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INSERT INTO `cyanodb_citations` VALUES (1,'KOMÁREK J., KAŠTOVSKÝ J., MAREŠ J., JOHANSEN J.R.',2014,'Taxonomic classification of cyanoprokaryotes (cyanobacterial genera) 2014, using a polyphasic approach','Preslia. <strong>86</strong>: 295–335',NULL,'http://www.preslia.cz/P144Komarek.pdf',0),(9,'ANAGNOSTIDIS K.',2001,'Nomenclatural changes in cyanoprokaryotic order Oscillatoriales','Preslia, Praha <strong>73</strong>(4): 359-375',NULL,NULL,0),(10,'BLANCHARD, F.N.',1913,'Two new species of Stigonema','Rhodora 15: 192-200',NULL,'https://www.archive.org/download/mobot31753003413363/mobot31753003413363.pdf',0),(11,'BOHUNICKÁ, M., JOHANSEN, J.R. et FUČÍKOVÁ, K.',2011,'<em>Tapinothrix clintonii</em> sp. nov. (Pseudanabaenaceae, Cyanobacteria), a new species at the nexus of five genera','Fottea <strong>11</strong>(1): 127–140.',NULL,'[pdf]fottea_fot-201101-0013.pdf',0),(12,'BÖCHER, T.W.',1950,'Structure and biology of four speciesof the Stigonemataceae from a shallow pool at Ivigtut','Meddelelser om Grønland 147(5): 1-21',NULL,'',0),(13,'BRANCO L.H.Z., KOMÁREK J., AZEVEDO M.T.P., SANT\'ANNA C.L. et WATANABE M.',2006,'The cyanobacterial genus<em> Cyanoarbor</em> (Chroococcales, Entophysalidaceae) and its occurrence in Brazil','Nova Hedwigia <strong><strong>82</strong></strong> (3-4): 365 - 380',NULL,NULL,0),(14,'CAISOVÁ, L.',2006,'<em>Pleurocapsa cuprea</em>, originally described as blue – green alga, is a eukaryotic alga similar to the species <em>Hildenbrandia rivularis</em> (Rhodophyta) [<em>Pleurocapsa cuprea</em>, popsaná jako sinice, je eukaryotní řasa z blízkosti druhu <em>Hildenbrandia rivularis</em> (Rhodophyta)]','Czech Phycology <strong>6</strong>: 69-76, 2006',NULL,'[pdf]fottea_fot-200601-0006.pdf',0),(15,'CASAMATTA D.A., GOMEZ S.R. et JOHANSEN J.R.',2006,'<em>Rexia erecta</em> gen. et sp. nov. and <em>Capsosira lowei </em>sp. nov., two newly described cyanobacterial taxa from the Great Smoky Mountains National Park (USA)','Hydrobiologia <strong>561</strong>: 13 - 26',NULL,NULL,0),(16,'CASAMATTA D.A, JOHANSEN J.R., VIS M.L. & BROADWATER S.T.',2005,'Molecular and morphological characterization of ten polar and near-polarstrains within the Oscillatoriales (Cyanobacteria)','Journal of Phycology 41: 421 - 438',NULL,'https://doi.org/10.1111/j.1529-8817.2005.04062.x',0),(17,'CHATTERJEE S. et KESHRI J.P.',2005,'<em>Borzia </em>(Cyanophyta) in West Bengal, India, with description of B-indica sp nov','Cryptogamie, Algologie <strong>26</strong>(4): 331 - 336.',NULL,NULL,0),(18,'FIORE M.F., SANT\'ANNA C.L.,  AZEVEDO M.T.P., KOMÁREK J., KAŠTOVSKÝ J., SULEK J. et  LORENZI A.S.',2007,'The cyanobacterial genus <em>Brasilonema</em>, gen. nov., a molecular and phenotypic evaluation','Journal of Phycology <strong>43</strong> (4): 789-798',NULL,NULL,0),(19,'FLECHTNER V.R., JOHANSEN J.R. et BELNAP J.',2008,'The biological soil crusts of the San Nicolas Island: Enigmatic algae from a geographically isolated ecosystem','Western North American Naturalist <strong>68</strong>(4): 405-436',NULL,'',0),(20,'HAUER T.',2000,'A comparison of the phytoplankton of fishponds with the field– and forest – catch basin in neighbourhood of Branišov. Bc. thesis [in Czech] – 12p','Faculty of Biological Sciences, The University of South Bohemia, České Budějovice, Czech Republic - unpublished',NULL,NULL,0),(21,'HOFFMANN L., KOMÁREK J. et KAŠTOVSKÝ J.',2005,'System of Cyanoprokaryotes (Cyanobacteria) - state in 2004','Arch. Hydrobiol./Algolgological Studies <strong>117</strong>: 95 - 115',NULL,NULL,0),(22,'JOHANSEN J.R., OLSEN, C.E., LOWE R.L., FUČÍKOVÁ K. et CASAMATTA D.A.',2008,'<em>Leptolyngbya</em> species from selected seep walls in the Great Smoky Mountains National Park','Algological Studies <strong>126</strong>: 21-36',NULL,NULL,0),(23,'JOHANSEN, J.R., ŘEHÁKOVÁ, K. et ACKER, F.',2011,'<em>Tapinothrix ozarkiana</em> sp. nov., with notes on distribution for the genus in North America','Fottea <strong>11</strong>(1): 141–148',NULL,'[pdf]fottea_fot-201101-0014.pdf',0),(24,'JOOSTEN A.M.T.',2006,'Flora of the Blue-green algae of the Netherlands I','239pp, KMNV Publishing, Utrecht.',NULL,NULL,0),(25,'KAŠTOVSKÝ, J., FUČÍKOVÁ, K., HAUER, T. et BOHUNICKÁ, M.',2011,'Microvegetation on the top of Mt. Roraima, Venezuela','Fottea <strong>11</strong>(1): 171–186.',NULL,'[pdf]fottea_fot-201101-0017.pdf',0),(26,'KOMÁREK J.',1992,'Diversita a moderní klasifikace sinic (Cyanoprocaryota) [Diversity and modern classification of Cyanobacteria (Cyanoprokaryota)','inaugural dissertation, not published',NULL,NULL,0),(27,'KOMÁREK J.',2001,'Review of cyanoprokaryotic genus<em> Romeria</em>','Czech Phycology <strong>1</strong>: 5 - 19',NULL,'[pdf]fottea_fot-200101-0002.pdf',0),(28,'KOMÁREK J.',2003,'Two <em>Camptylonemopsis</em> species (cyanoprokaryotes) from &quot;Mata Atlantica&quot; in Coastal Brazil','Preslia <strong>75</strong>: 223 - 232',NULL,'http://www.preslia.cz/P032CKom.pdf',0),(29,'KOMÁREK J.',2008,'The cyanobacterial genus <em>Macrospermum</em>','Fottea <strong>8</strong>(1): 79-86',NULL,'[pdf]fottea_fot-200801-0003.pdf',0),(30,'KOMÁREK J. et ANAGNOSTIDIS K.',1998,'Cyanoprokaryota 1. Teil: Chroococcales','In: ETTL H., GÄRTNER G., HEYNIG H. &amp; MOLLENHAUER D. (eds): Süsswasserflora von Mitteleuropa 19/1, Gustav Fischer, Jena-Stuttgart-Lübeck-Ulm, 548 pp.',NULL,NULL,0),(31,'KOMÁREK J. et ANAGNOSTIDIS K.',2005,'Cyanoprokaryota 2. Teil/ 2nd Part: Oscillatoriales','In: BÜDEL B., KRIENITZ L., GÄRTNER G. &amp; SCHAGERL M. (eds): Süsswasserflora von Mitteleuropa 19/2, Elsevier/Spektrum, Heidelberg, 759 pp.',NULL,NULL,0),(32,'KOMÁREK J. et KOMÁRKOVÁ J.',2002,'Review of the European <em>Microcystis</em>-morphospecies (Cyanoprokaryotes) from nature','Czech Phycology <strong>2</strong>: 1 - 24',NULL,'[pdf]fottea_fot-200201-0001.pdf',0),(33,'KOMÁREK J. et KOMÁRKOVÁ J.',2003,'Phenotype diversity of the cyanoprokaryotic genus <em>Cylindrospermopsis </em>(Nostocales); review 2002','Czech Phycology <strong>3</strong>: 1 - 30',NULL,NULL,0),(34,'KOMÁREK J. et KOMÁRKOVÁ J.',2004,'Taxonomic review of the cyanoprokaryotic genera <em>Planktothrix</em> and <em>Planktothricoides</em>','Czech Phycology <strong>4</strong>: 1-18',NULL,'[pdf]fottea_fot-200401-0001.pdf',0),(35,'KOMÁREK J. et KOMÁRKOVÁ-LEGNEROVÁ J.',2007,'Taxonomic evaluation of the cyanobacterial microflora from alkaline marshes of northern Belize. 1. Phenotypic diversity of coccoid morphotypes','Nova Hedwigia <strong>84</strong>(1-2): 65-111',NULL,NULL,0),(36,'KOMÁREK J. et ZAPOMĚLOVÁ E.',2007,'Planktic morphospecies of the cyanobacterial genus <em>Anabaena </em>= subg.  <em>Dolichospermum </em>– 1. part: coiled types','Fottea <strong>7</strong>: 1–31',NULL,'[pdf]fottea_fot-200701-0001.pdf',0),(37,'KOMÁREK J., ZAPOMĚLOVÁ E. et HINDÁK F.',2010,'<em>Cronbergia</em> gen. nov., a new cyanobacterial genus (Cyanophyta) with a special strategy of heterocyte formation','Cryptogamie, Algologie <strong>31</strong>(3): 321-341',NULL,NULL,0),(38,'KOMÁRKOVÁ J., JEZBEROVÁ J., KOMÁREK O. et ZAPOMĚLOVÁ E.',2010,'Variability of <em>Chroococcus </em>(Cyanobacteria) morphospecies with regard to phylogenetic relationships','Hydrobiologia <strong>639</strong>: 69-83',NULL,NULL,0),(39,'KORELUSOVÁ, J., KAŠTOVSKÝ, J. et KOMÁREK, J.',2009,'Heterogeneity of the cyanobacterial genus <em>Synechocystis</em> and description of a new genus <em>Geminocystis</em>','Journal of Phycology <strong>45</strong>: 928-937',NULL,'https://doi.org/10.1111/j.1529-8817.2009.00701.x',0),(40,'LIN Y.-M. et XIAO H.-X.',2004,'A new species of <em>Asterocapsa </em>(Cyanophyta) from Jilin Province, China','Bull. of Botanical Research <strong>24</strong>(4): 385-386<br>',NULL,NULL,0),(41,'MAREŠ, J.',2010,'<em> Anabaena fuscovaginata</em> (Nostocales), a new cyanobacterial species from periphyton of the freshwater alkaline marsh of Everglades, South Florida, USA','Fottea <strong>10</strong>(2): 235-243',NULL,'[pdf]F10-2-2010-05.pdf',0),(42,'MAREŠ J., KAŠTOVSKÝ J., MCGREGOR G. et KOMÁREK J.',2008,'The little known pseudofilamentous cyanobacterium <em>Wolskyella</em> (Synechococcales)','Nova Hedwigia <strong>87</strong>: 221-230',NULL,NULL,0),(43,'MARGHERI M.C., VENTURA S., KAŠTOVSKÝ J. et KOMÁREK J.',2008,'The taxonomic validation of the cyanobacterial genus Halothece','Phycologia <strong>47</strong>(5): 477-486',NULL,NULL,0),(44,'MATALONI G. et KOMÁREK J.',2004,'<em>Gloeocapsopsis aurea</em>, a new subaerophytic cyanobacterium from maritime Antarctica','Polar. Biol. <strong>27</strong>: 623-628',NULL,NULL,0),(45,'McGREGOR G.B.',2007,'Freshwater Cyanoprokaryota of North-Eastern Australia. 1. Oscillatoriales','Flora of Australia Supplementary Series No. 24.  Australian Biological Resources Study, Canberra.',NULL,NULL,0),(46,'MIYASHITA H., IKEMOTO H., KURANO N., MIYACHI S. & CHIHARA M.',2003,'<em>Acaryochloris marina</em> gen. et sp. nov. (Cyanobacteria), an oxygenic photosynthetic prokaryote containing chl <em>D</em> as a major pigment','J. Phycol. <strong>39</strong>: 1247 - 1253',NULL,'https://doi.org/10.1111/j.0022-3646.2003.03-158.x',0),(47,'CHOI D.H., NOH J.H., LEE C.M. et RHO S.',2008,'<em>Rubidibacter lacunae</em> gen. nov., sp. nov., a unicellular, phycoerythrin-containing cyanobacterium isolated from seawater of Chuuk lagoon, Micronesia','Int. J. Systematic and Evolutionary Microbiology <strong>58</strong>: 2807-2811&nbsp;',NULL,'https://dx.doi.org/10.1099/ijs.0.65798-0',0),(48,'RAJANIEMI P., KOMÁREK J., WILLAME R., HROUZEK P., KAŠTOVSKÁ K., HOFFMANN L. et SIVONEN K.',2005,'Taxonomic consequencesfrom the combined molecular and phenotype evaluation of selected <em>Anabaena</em> and <em>Aphanozomenon</em> strains','Arch. Hydrobiol./Algological Studies <strong>117</strong>: 371 - 391',NULL,NULL,0),(49,'RASOULOUNIRIANA D., SIBONI N., BEN-DOV E., KRAMARSKY-WINTER E., LOYA Y. et KUSHMARO A.',2009,'<em>Pseudoscillatoria coralii</em> gen. nov., sp. nov., a cyanobacterium associated with coral black band disease (BBD)','Diseases of aquatic organisms <strong>87</strong>: 91-96&nbsp;',NULL,NULL,1),(50,'ŘEHÁKOVÁ, K., JOHANSEN, J.R., CASAMATTA, D.A., XUESON, L. & VINCENT, J.',2007,'Morphological and molecular characterization of selected desert soil cyanobacteria: three species new to science including Mojavia pulchra gen. et sp. nov','Phycologia <strong>46</strong> (5): 481 - 502',NULL,'https://doi.org/10.2216/06-92.1',0),(51,'ROTT E.',2008,'<em>Chamaesiphon komárekii</em> species nova, a new benthic chroococcalean species (Cyanophyta/Cyanobacteria) from western coniferous forest streams in British Columbia','Algological Studies <strong>126</strong>: 37-46',NULL,NULL,0),(52,'SANT\'ANNA, C.L., AZEVEDO, T.M.P., KAŠTOVSKÝ, & KOMÁREK, J.',2010,'Two form–genera of aerophytic heterocytous cyanobacteria from Brasilian rainy forest \'Mata Atlântica\'','Fottea <strong>10</strong>(2): 217-228',NULL,'[pdf]fottea_fot-201002-0003.pdf',0),(53,'SEENAYA, G. & SUBBA RAJU, N.',1972,'On the Ecology and Systematic Position of the Alga known as<em>&nbsp;Anabaenopsis raciborskii</em> (Wolosz.) Elenk. and a Critical Evaluation of the Forms Described under Genus <em>Anabaenopsis</em>','In: DESIKACHARY T.V: Taxonomy and Biology of Blue-green Algae. - p. 52 - 57, University of Madras, Madras.',NULL,'',0),(54,'STRUNECKÝ, O., ELSTER, J. et KOMÁREK, J.',2011,'Taxonomic revision of the freshwater cyanobacterium „<em>Phormidium</em>“ <em>murrayi </em>= <em>Wilmottia murrayi</em>','Fottea <strong>11</strong>(1): 57–71.',NULL,'[pdf]F11-1-2011-07.pdf',0),(55,'SUDA S., WATANABE M.M., OTSUKA S., MAHAKAHANT A., YONGMANITHAI W., NOPARTNARAPORN N., LIU Y. et DAY J.G.',2002,'Taxonomic revision of water-bloom-forming species of oscillarioid cyanobacteria','International Journal of Systematic and Evolutionary Microbiology <strong>52</strong>: 1577 - 1595',NULL,NULL,0),(56,'TATON A., WILMOTTE A., ŠMARDA J., ELSTER J. et KOMÁREK J.',2011,'Plectolyngbya hodgsonii: a novel filamentous cyanobacterium from Antarctic lakes','Polar Biology <strong>34</strong>: 181-191',NULL,'https://dx.doi.org/10.1007/s00300-010-0868-y',0),(57,'TSENG C.K. et MAOSEN H.',1983,'On a new species of Camptylonemopsis (Cyanophyta) from South China','Chinese Journal of Oceanology and&nbsp; Limnology <strong>1</strong>(3):361-366',NULL,NULL,0),(58,'UHER, B.',2007,'Morphological characterization of three subaerial <em>Calothrix </em>species (Nostocales, Cyanobacteria)','Fottea <strong>7</strong>: 33–38',NULL,'[pdf]fottea_fot-200701-0002.pdf',0),(59,'VACCARINO M.A. et JOHANSEN J.R.',2011,'<em>Scytonematopsis contorta</em> sp. nov. (Nostocales), a new species from the Hawaiian Islands','Fottea <strong>11</strong>(2): 149–161',NULL,'[pdf]fottea_fot-201101-0015.pdf',0),(60,'WACKLIN P., HOFFMANN L. et KOMÁREK J.',2009,'Nomenclatural validation of the genetically revised cyanobacterial genus Dolichospermum (RALFS ex BORNET et FLAHAULT) comb. nova','Fottea <strong>9</strong>(1): 59–64',NULL,'[pdf]fottea_fot-200901-0005.pdf',0),(61,'WERNER V.R., SANT\'ANNA C.L. et AZEVEDO M.T.P.',2008,'<em>Cyanoaggregatum brasiliense</em> gen. et sp. nov., a new chroococcal Cyanobacteria from Southern Brasil','Revista Brasil. Botanica <strong>31</strong>(3): 491-497',NULL,NULL,0),(62,'ZAPOMĚLOVÁ E., JEZBEROVÁ J., HROUZEK P., HISEM D., ŘEHÁKOVÁ K. et KOMÁRKOVÁ J.',2009,'Polyphasic characterisation of three strains of <em>Anabaena reniformis</em> and <em>Aphanizomenon aphanizomenoides</em> (Cyanobacteria) and their reclasification to <em>Sphaerospermum</em> gen. nov. (incl. <em>Anabaena kisseleviana</em>)','Journal of Phycology <strong>45</strong>: 1363-1373',NULL,NULL,0),(63,'ZAPOMĚLOVÁ E., JEZBEROVÁ J., HROUZEK P., HISEM D., ŘEHÁKOVÁ K. et KOMÁRKOVÁ J.',2010,'Polyphasic characterisation of three strains of <em>Anabaena reniformis</em> and <em>Aphanizomenon aphanizomenoides</em> (Cyanobacteria) and their reclasification to <em>Sphaerospermum</em> gen. nov. (incl. <em>Anabaena kisseleviana</em>) (45: 1363-1373). Nomenclatural note','Journal of Phycology <strong>46</strong>: 415',NULL,NULL,0),(69,'ABED R.M.M., GARCIA-PICHEL F. & HERNADEZ-MARINÉ M.',2002,'Polyphasic characterization of benthic, moderately halophilic, moderately thermophilic cyanobacteria with very thin trichomes and the proposal of <em>Halomicronema excentricum</em> gen. nov., sp. nov.','Arch. Microbiol., 177: 369',NULL,'http://dx.doi.org/10.1007/s00203-001-0390-2',0),(70,'CHEN M., LI Y., BIRCH D. & WILLOWS R.D.',2012,'A cyanobacterium that contains chlorophyll f – a red-absorbing photopigment','FEBS Letters <strong>586</strong>(19): 3249–3254',NULL,'http://dx.doi.org/10.1016/j.febslet.2012.06.045',0),(71,'AGUIAR R., FIORE M.F., FRANCO M.W., VENTRELLA M.C:, LORENZI A.S., VANETTI C.A. et ALFENAS A.C.',2008,'A novel epiphytic cyanobacterial species from the genus Brasilonema causing damage to Eucalyptus leaves','&nbsp;J. Phycol. <strong>44</strong>:1325',NULL,'http://dx.doi.org/10.1111/j.1529-8817.2008.00584.x',0),(73,'HAUER, T., BOHUNICKÁ, M., JOHANSEN, J.R., MAREŠ, J. & BERRENDERO-GÓMEZ, E.',2014,'Reassessment of the cyanobacterial family Microchaetaceae and establishment of new families Tolypothrichaceae and Godleyaceae','Journal of Phycology 50: 1089-1100',NULL,'https://doi.org/10.1111/jpy.12241',0),(74,'BOHUNICKÁ, M., PIETRASIAK, N., JOHANSEN, J.R., BERRENDERO-GÓMEZ, E., HAUER, T., GAYSINA, L.A. & LUKEŠOVÁ A.',2015,'<em>Roholtiella</em>, gen. nov. (Nostocales, Cyanobacteria)—a tapering and branching cyanobacteria of the family Nostocaceae','Phytotaxa 197(2): 84-103',NULL,'http://dx.doi.org/10.11646/phytotaxa.197.2.2',0),(75,'KOMÁREK J., KAŠTOVSKÝ, J. & JEZBEROVÁ, J.',2011,'Phylogenetic and taxonomic delimitation of the cyanobacterial genus <em>Aphanothece </em>Nägeli<em>&nbsp;</em>and description of <em>Anathece </em>gen. novum','European Journal of Phycology 46(3): 315-326.',NULL,'http://dx.doi.org/10.1080/09670262.2011.606373',0),(76,'HINDÁK, F.',1975,'Einige neue und interessante Planktonblaualgen aus der Westslowakei','Algological Studies 13: 330-353',NULL,'',0),(78,'HINDÁK, F.',1982,'On some planctic coccoid blue-green algae characteristic by Fe-precipitates.','Algological Studies 32: 241-258',NULL,'',0),(79,'HICKEL, B.',1985,'<em>Cyanonephron styloides </em>gen. et sp. nov., a new chroococcal blue-green alga (Cyanophyta) from a brackish lake','Algological Studies 38/38: 99-104',NULL,'',0),(80,'Komárková-Legnerová, J.',1991,'<em>Epigloeosphaera</em>, a new cyanophyte genus from Nordic lakes','Algological Studies 62: 7-12',NULL,'',0),(81,'MOREIRA, D., TAVERA R., BENZERARA, K., SKOURI-PANET, F., COURADEAU, E., LOUSSERT FONTA, C., NOVELO, E., ZIVANOVIC, Y. & LÓPEZ-GARCÍA, P.',2017,'Description of <em>Gloeomargarita lithophora</em> gen. nov., sp. nov., a thylakoid-bearing basal-branching cyanobacterium with intracellular carbonates, and proposal for Gloeomargaritales ord. nov.','International Journal of Systematic and Evolutionary Microbiology 67: 653-658',NULL,'https://doi.org/10.1099/ijsem.0.001679',0),(82,'GEITLER, L.',1942,'Schizophyta: Klasse Schizophyceae. In: Die natürlichen Pflanzenfamilien, Sweite Auflage','&nbsp; In: Engler, A. &amp; Prantl, K. Eds., Vol.1b, 232 pp. &nbsp;Leipzig: Wilhelm Engelmann.',NULL,'',0),(83,'ERCEGOVIĆ, A.',1925,'Litofitska vegetacija vapnenaca i dolomita u Hrvatskoj. [La végétation des lithophytes sur les calcaires et les dolomites en Croatie.]','Acta Botanica Instituti Botanici Universitatis Zagrebensis 1:64-114',NULL,'',0),(84,'HOWE, M.A.',1932,'The geologic importance of the lime secreting algae&nbsp;','Professional Papers. United States Geological Survey 170: 57-64',NULL,'',0),(85,'DVOŘÁK, P., HINDÁK, F., HAŠLER, P., HINDÁKOVÁ, A. & POULÍČKOVÁ, A.',2014,'Morphological and molecular studies of<em> Neosynechococcus sphagnicola</em>, gen. et sp. nov. (Cyanobacteria, Synechococcales)','Phytotaxa 170 (1): 24–34',NULL,'http://dx.doi.org/10.11646/phytotaxa.170.1.3',0),(87,'Hindák, F.',1988,'Contribution to the taxonomy of some cyanophyte genera','Preslia 60: 289-308',NULL,'',0),(88,'CLEMENTS, F.E. & SCHANTZ, H.L.',1909,'A new genus of blue-green algae','Minnesota Botanical Studies 4: &nbsp;133-135',NULL,'https://www.archive.org/download/minnesotabotanic04geol/minnesotabotanic04geol.pdf',0),(89,'DANGEARD, P.J.L.',1941,'Chroococcales, genre <em>Mantellum </em>gen. nov','Le Botaniste 30: &nbsp;129-131',NULL,'',0),(90,'Hickel, B.',1991,'Two new chroococcal cyanophytes from a brackish environment (Schlei-Fjord), Germany.&nbsp;','Algological Studies 64: &nbsp;97-104',NULL,'',0),(91,'Rippka, R. & Cohen-Bazire, G.',1983,'&nbsp;The Cyanobacteriales: a legitimate order based on the type strain <em>Cyanobacterium stanieri</em>?','Annales de l\'Institut Pasteur, Microbiologie 134B: &nbsp;21-36',NULL,'',0),(92,'COUTINHO, F., TSCHOEKE, D.A., THOMPSON, F. & THOMPSON, C.',2016,'Comparative genomics of <em>Synechococcus</em> and proposal of the new genus <em>Parasynechococcus</em>','PeerJ',NULL,'https://doi.org/10.7717/peerj.1522',0),(93,'Chisholm, S. W., Frankel, S. L., Goericke, R., Olson, R. J., Palenik,  B., Waterbury, J. B., West-Johnsrud, L. & Zettler, E. R.',1992,'&nbsp;<em>Prochlorococcus marinus</em> nov. gen. nov. sp.: an oxyphototrophic marine prokaryote containing divinyl chlorophyll a and b.','Archives of Microbiology 157: 297-300',NULL,'',0),(94,'BUELL, H.F.',1938,'A community of blue-green algae in a Minnesota pond','Bulletin of the Torrey Botanical Club 65: 377-396',NULL,'',0),(95,'LEMMERMANN, E.',1899,'Ergebnisse einer Reise nach dem Pacific. (H. Schauinsland 1896/97.) Planktonalgen','<em>Abhandlungen herausgegeben vom Naturwissenschaftlichen zu Bremen</em> 16: &nbsp;313-398',NULL,'https://www.archive.org/download/abhandlungenhera16natu/abhandlungenhera16natu.pdf',0),(96,'Hindák, F.',1988,'&nbsp;Taxonomic position of two cyanophyte genera, <em>Cyanostylon</em> Geitler and <em>Siphonosphaera</em> gen. nov.&nbsp;','Algological Studies 49: &nbsp;411-423',NULL,'',0),(97,'ELENKIN, A.A.',1938,'Monographia algarum cyanophycearum aquidulcium &nbsp;et terrestrium in finibus URSS inventarum. (Sinezelenye vodorosli SSSR).<em>&nbsp; </em>Pars spec. (1-2). &nbsp;pp. 1-1908.','Moskva-Leningrad: Izd. AN SSSR.',NULL,'',0),(98,'ELENKIN, A.A.',1933,'O sistematicheskom podrazdenii poryadka Chroococcales Geitler (1925)','Trudy Botanicheskogo Instituta Akademii Nauk SSSR, Ser. 2, Sporovye Rasteniya 1: &nbsp;17-21.',NULL,'',0),(99,'PASCHER, A.',1914,'&nbsp;Über Symbiosen von Spaltpilzen und Flagellaten mit Blaualgen','<em>Berichte der Deutschen Botanischen Gesellschaft</em> 32(5): &nbsp;339-352',NULL,'https://www.archive.org/download/mobot31753002189998/mobot31753002189998.pdf',0),(100,'VAZ,M.G.M.V., GENUÁRIO, D.B., ANDREOTE, A.P.D., MALONE, C.F.S.,  SANT’ANNA, C.L., BARBIERO, L. & FIORE, M.F.',2015,'<em>Pantanalinema </em>gen. nov. and <em>Alkalinema</em> gen. nov.: novel pseudanabaenacean genera (Cyanobacteria) isolated from saline–alkaline lakes','International Journal of Systematic and Evolutionary Microbiology (2015), 65, 298–308',NULL,'https://dx.doi.org/10.1099/ijs.0.070110-0',0),(101,'Komárek, J. & Lukavský, J.',1988,'Arthronema, a new cyanophytegenus from Afro-Asian deserts','Algological Studies 50-53: 249-267',NULL,'',0),(102,'Anagnostidis K. & Komárek J.',1988,'Modern approach to the &nbsp;classification system of cyanophytes 3 - <em>Oscillatoriales.&nbsp;</em>','Algological Studies 50-53: 327-472',NULL,'',0),(103,'HAŠLER, P., DVOŘÁK, P. & POULÍČKOVÁ, A.',2014,'&nbsp;A new genus of filamentous epipelic cyanobacteria, <em>Johansenia</em>','&nbsp;Preslia 86: 81-94',NULL,'',0),(104,'HAŠLER, P., DVOŘÁK, P. & POULÍČKOVÁ, A.',2014,'<em>Johanseninema</em>, a corrected name for a recently described genus of filamentous epipelic cyanobacteria','Preslia 86: 293-294',NULL,'',0),(105,'MEFFERT, M.-E.',1988,'<em>Limnothrix</em> Meffert nov. gen. - the unsheathed planktic cyanophycean filaments with polar and central gas vacuoles','Algological Studies 50-53: &nbsp;269-276',NULL,'',0),(106,'DVOŘÁK, P., JAHODÁŘOVÁ, E., HAŠLER, P., GUSEV, E. & POULÍČKOVÁ, A.',2015,'&nbsp;A new tropical cyanobacterium <em>Pinocchia polymorpha</em> gen. et sp. nov. derived from the genus <em>Pseudanabaena</em>','Fottea 15(1): &nbsp;113-120',NULL,'https://doi.org/10.5507/fot.2015.010',0),(107,'LAUTERBORN, R.',1915,'Die sapropelische Lebewelt. Ein Beitrag zur Biologie des Faulschlammes natürlicher Gewässer','Verhandlungen des Naturhistorisch-Medizinischen Vereins zu Heidelberg ser. 2, 13: &nbsp;395-481',NULL,'',0),(108,'RASOULOUNIRIANA, D., SIBONI, N., BEN-DOV, E., KRAMARSKY-WINTER, E., LOYA, Y. & KUSHMARO, A.',2009,'<em>Pseudoscillatoria coralii</em> gen. nov., sp. nov., a cyanobacterium associated with coral black band disease (BBD)&nbsp;','Diseases of Aquatic Organisms 87: &nbsp;91-96',NULL,'',0),(109,'UMEZAKI, I.',1962,'[News and Notes] <em>Yonedaella</em> nom. nov.&nbsp;','Taxon 10: &nbsp;204',NULL,'',0),(110,'DADHEECH, P.K., MAHMOUD, H., KOTUT, K. & KRIENITZ, L.',2012,'<em>Haloleptolyngbya alcalis</em> gen. et sp. nov., a new filamentous cyanobacterium from the soda lake Nakuru, Kenya','Hydrobiologia 691: &nbsp;269-283',NULL,'https://doi.org/10.1007/s10750-012-1080-6',0),(111,'MISCOE, L.H., JOHANSEN, J.R., VACCARINO, M.A., PIETRASIAK, N. & SHERWOOD,  A.R.',2016,'The diatom flora and cyobacteria from caves on Kauai, &nbsp;Hawaii. II. Novel cyanobacteria from caves on Kauai, Hawaii','<em>Bibliotheca Phycologica</em> 120: &nbsp;75-152',NULL,'',0),(113,'HENTSCHKE, G.S., JOHANSEN, J.R., PIETRASIAK, N., RIGONATO, J., FIORE, M.F. & SANT´ANNA, C.L.',2017,'Komarekiella atlantica gen. et sp. nov. (Nostocaceae, Cyanobacteria): a new subaerial taxon from the Atlantic Rainforest and Kauai, Hawaii','Fottea 17(2): 178-190',NULL,'https://www.fottea.czechphycology.cz/pdfs/fot/2017/02/04.pdf',0),(114,'ALVARENGA, D.O., ANDREOTE, A.P.D., BRANCO, L.H.Z & FIORE, M.F.',2017,'Kryptousia macronema gen. nov., sp. nov. and Kryptousia microlepis sp. nov., nostocalean cyanobacteria isolated from phyllospheres','International Journal of Systematic and Evolutionary Microbiology',NULL,'https://doi.org/10.1099/ijsem.0.002109',0),(115,'NÄGELI, C.',1849,'Gattungen der einzelliger Algen physiologisch und systematisch bearbeitet','Friedrich Schultess, Zürich, 139 p.&nbsp;',NULL,'https://www.archive.org/download/gattungeneinzell00ng/gattungeneinzell00ng.pdf',0),(116,'CASAMATTA, D., STANIĆ, D., GANTAR, M. & RICHARDSON. L.L.',2012,'Characterization of Roseofilum reptotaenium (Oscillatoriales, Cyanobacteria) gen. et sp. nov. isolated from Caribbean black band disease','Phycologia 51(5): 489–499',NULL,'https://doi.org/10.2216/11-10.1',0),(117,'SCIUTO, K. & MORO, I.',2016,'Detection of the new cosmopolitan genus Thermoleptolyngbya (Cyanobacteria, Leptolyngbyaceae) using the 16S rRNA gene and 16S–23S ITS region','Molecular Phylogenetics and Evolution 105: 15–35',NULL,'https://doi.org/10.1016/j.ympev.2016.08.010',0),(118,'JOHANSEN, J.R., KOVÁČIK, Ľ., CASAMATTA, D.A., FUČÍKOVÁ, K. & KAŠTOVSKÝ, J.',2011,'Utility of 16S-23S ITS sequence and secondary structure for recognition of intrageneric and intergeneric limits within cyanobacterial taxa: <em>Leptolyngbya corticola</em> sp. nov. (Pseudanabaenaceae, Cyanobacteria)','Nova Hedwigia 92(3–4): 283– 302',NULL,'https://doi.org/10.1127/0029-5035/2011/0092-0283',0),(119,'SONG, G.-F., JIANG, Y.-G. & LI, R.-H.',2015,'Scytolyngbya timoleontis, gen. et sp. nov. (Leptolyngbyaceae, Cyanobacteria): a novel false branching Cyanobacteria from China','Phytotaxa 224(1): 72–84',NULL,'http://dx.doi.org/10.11646/phytotaxa.224.1.5',0),(120,'RIGONATO, J., GAMA, W.A., ALVARENGA, D.A., BRANCO, L.H.Z., BRANDINI, F.P., GENUÁRIO, D.B. & FIORE M.F.',2016,'Aliterella atlantica gen. nov., sp. nov., and Aliterella antarctica sp. nov., novel members of coccoid Cyanobacteria','International Journal of Systematic and Evolutionary Microbiology 66: 2853–2861',NULL,'https://doi.org/10.1099/ijsem.0.001066',0),(121,'JAHODÁŘOVÁ, E., DVOŘÁK, P., HAŠLER, P. & POULÍČKOVÁ, A.',2017,'Revealing hidden diversity among tropical cyanobacteria: the new genus Onodrimia (Synechococcales, Cyanobacteria) described using the polyphasic approach','Phytotaxa 326(1): 28-40',NULL,'https://doi.org/10.11646/phytotaxa.326.1.2',0),(122,'CHATCHAWAN, T., KOMÁREK, J., STRUNECKÝ, O., ŠMARDA, J. & PEERAPORNPISAL, Y.',2012,'<em>Oxynema</em>, a new genus separated from the genus <em>Phormidium </em>(Cyanophyta)','Cryptogamie, Algologie 33(1): 41-59',NULL,'https://doi.org/10.7872/crya.v33.iss1.2011.041',0),(123,'ZAMMIT, G., BILLI, D. & ALBERTANO, P.',2012,'The subaerophytic cyanobacterium Oculatella subterranea (Oscillatoriales, Cyanophyceae) gen. et sp. nov.: a cytomorphological and molecular description','European Journal of Phycology 47(4) 341-354',NULL,'https://doi.org/10.1080/09670262.2012.717106',0),(124,'LAMPRINOU, V., CHRISTODOULOU, M., HERNÁNDEZ-MARINÉ, M., PARMAKELIS, A. & ECONOMOU-AMILI, A.',2016,'Spelaeonaias gen. nov., a new true-branched cyanobacterium from Cave Vlychada (Diros, Peloponnese, Greece)','Phytotaxa 282(3): 171-185',NULL,'https://dx.doi.org/10.11646/phytotaxa.282.3.1',0),(125,'DADHEECH, P.K., ABED, R.M.M., MAHMOUD, H., MOHAN M.K. & KRIENITZ, L.',2012,'Polyphasic characterization of cyanobacteria isolated from desert crusts, and the description of <em>Desertifilum tharense</em> gen. et sp. nov. (Oscillatoriales)','Phycologia 51(3): 260-270',NULL,'https://doi.org/10.2216/09-51.1',0),(126,'CAI, F.-F., CHEN, Y.-X., ZHU, M.-L., LI, X.-CH. & LI, R.-H.',2017,'<em>Desertifilum salkalinema</em> sp. nov. (Oscillatoriales, Cyanobacteria) from an alkaline pool in China','Phytotaxa 292(3): 262-270',NULL,'https://doi.org/10.11646/phytotaxa.292.3.6',0),(127,'SIEGESMUND, M.A., JOHANSEN, J.R., KARSTEN, U., & FRIEDL, T.',2008,'<em>Coleofasciculus </em>gen. nov. (Cyanobacteria): Morphological and molecular criteria for revision of the genus <em>​Microcoleus</em>​ Gomont​​​','Journal of Phycology 44: 1572-1585',NULL,'https://doi.org/10.1111/j.1529-8817.2008.00604.x',0),(128,'VÁZQUEZ-MARTÍNEZ, J., GUTIERREZ-VILLAGOMEZ, J.M., FONSECA-GARCÍA, C., RAMÍREZ-CHÁVEZ, E., MONDRAGÓN-SÁNCHEZ, M.L., PARTIDA-MARTÍNEZ, L., JOHANSEN, J.R. & MOLINA-TORRES, J.',2018,'<em>Nodosilinea chupicuarensis</em> sp. nov. (Leptolyngbyaceae, Synechococcales) a subaerial cyanobacterium isolated from a stone monument in central Mexico','Phytotaxa 334(2): 67182',NULL,'https://doi.org/10.11646/phytotaxa.334.2.6',0),(129,'BRITO, Â., RAMOS, V., MOTA, R., LIMA, S., SANTOS, A., VIEIRA, J., VIEIRA, C.P., KAŠTOVSKÝ, J., VASCONSELOS, V.M. & TAMAGNINI, P.',2017,'Description of new genera and species of marine cyanobacteria from the Portuguese Atlantic coast','Molecular Phylogenetics and Evolution 111: 18–34',NULL,'http://dx.doi.org/10.1016/j.ympev.2017.03.006',0),(130,'CANTONATI, M., KOMÁREK, J., HERNÁNDEZ.MARINÉ, M. & ANGELI, M.',2014,'New and poorly known coccoid species (Cyanoprokaryota) from the mid-depth and deep epilithon of a carbonate mountain lake','Freshwater Science 33(2): 548-556',NULL,'https://doi.org/10.1086/675931',0),(131,'MAREŠ, J. & CANTONATI, M.',2016,'Phylogenetic position of Geitleribactron purpureum (Synechococcales, Cyanobacteria/Cyanophyceae) and its implications for the taxonomy of Chamaesiphonaceae and Leptolyngbyaceae','Fottea 16(1): 104-111',NULL,'https://doi.org/10.5507/fot.2016.002',0),(132,'STRUNECKÝ, O., ELSTER, J. & KOMÁREK, J.',2011,'Taxonomic revision of the freshwater cyanobacterium „<em>Phormidium</em>“ <em>murrayi </em>= <em>Wilmottia murrayi</em>','Fottea 11(1): 57-71',NULL,'https://doi.org/10.5507/fot.2011.007',0),(133,'NOVIS, P.M. & VISNOVSKY G.',2011,'Novel alpine algae from New Zealand: Cyanobacteria','Phytotaxa 22: 1-24',NULL,'https://doi.org/10.11646/phytotaxa.22.1.1',0),(134,'DE TONI, J.B.',1936,'Noterelle di nomenclatura algologica. VIII. Terzo elenco di Missoficee omonime.','<span dir=\'ltr\'>Morcelliana</span>, 6 p.',NULL,'',0),(135,'KÜTZING, F.T.',1843,'<span itemprop=\'name\'>Phycologia generalis : oder, Anatomie, physiologie und systemkunde der tange</span>','<span itemprop=\'publisher\'><span itemprop=\'name\'>F. A. Brockhaus</span></span>, Leipzig, 458 p.',NULL,'https://doi.org/10.5962/bhl.title.4746',0),(136,'GOLD-MORGAN, M., MONTEJANO, G. & KOMÁREK, J.',1996,'Freshwater epiphytic Chamaesiphonaceae from Central Mexico','Archiv für Hydrobiologie/Algological Studies 83: 257-271',NULL,'',0),(137,'TAVERA, R. & KOMÁREK, J.',1996,'Cyanoprokaryotes in volcanic lake Alchichica, Puebla State, Mexico','Archiv für Hydrobiologie, Algological Studies 83: 511-538',NULL,'',0),(138,'HAŠLER, P., DVOŘÁK, P., POULÍČKOVÁ, A. & CASAMATTA, D.A.',2014,'A novel genus <em>Ammasolinea </em>gen. nov. (Cyanobacteria) isolated from subtropical epipelic habitats','Fottea 14(2):',NULL,'https://doi.org/10.5507/fot.2014.018',0),(139,'JAHODÁŘOVÁ, E., DVOŘÁK, P., HAŠLER, P., HOLUŠOVÁ, K. & POULÍČKOVÁ, A.',2018,'Elainella gen. nov.: a new tropical cyanobacterium characterized using a complex genomic approach','European Journal of Phycology 53(1): 39-51',NULL,'https://doi.org/10.1080/09670262.2017.1362591',0),(140,'MÜHLSTEINOVÁ, R., JOHANSEN, J.R., PIETRASIAK, N., MARTIN, M.P., OSORIO-SANTOS, K. & WARREN, S.D.',2014,'Polyphasic characterization of <em>Trichocoleus desertorum</em> sp. nov. (Pseudanabaenales, Cyanobacteria) from desert soils and phylogenetic placement of the genus <em>Trichocoleus</em>','Phytotaxa 163(5): 241-261',NULL,'http://dx.doi.org/10.11646/phytotaxa.163.5.1',0),(141,'ENGENE, N., PAUL, V.J., BYRUM, T., GERWICK, W.H., THOR, A. & ELLISMAN, M.H.',2013,'Five chemically rich species of tropical marine cyanobacteria of the genus <em>Okeania </em>gen. nov. 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Lyngbya bouillonii sp. nov., a remarkable tropical reef-inhabiting blue-green alga','Belgian Journal of Botany 124(1): 82-88',NULL,'',0),(144,'CLAUS, G.',1962,'Beiträge zur Kenntnis der Algenflora der Abaligeter Höhle','Hydrobiologia 19(2):192-222',NULL,'',0),(145,'GOMONT, M.',1892,'Monographie des Oscillariées (Nostocacées homocystées)','Annales des Sciences Naturelles, Botanique, Série 7, 15: &nbsp;263-368',NULL,'https://www.archive.org/download/annalesdesscienc7151unse/annalesdesscienc7151unse.pdf',0),(146,'PERKENSON, R.B. III, JOHANSEN, J.R., KOVÁČIK, Ľ, BRAND, J., KAŠTOVSKÝ, J., CASAMATTA, D.A.',2011,'A unique Pseudanabaenalean (Cyanobacteria) genus Nodosilinea gen. nov. based on morphological and molecular data','Journal of Phycology 47: 1397-1412',NULL,'https://dx.doi.org/10.1111/j.1529-8817.2011.01077.x',0),(147,'LI, Z. & BRAND, J.',2007,'Leptolyngbya nodulosa sp. nov. (Oscillatoriaceae), a Subtropical Marine Cyanobacterium that Produces a Unique Multicellular Structure','Phycologia 46 (4): 396-401',NULL,'https://doi.org/10.2216/06-89.1',0),(148,'LEMMERMANN, E.',1899,'Ergebnisse einer Reise nach dem Pacific. (H. Schauinsland 1896/97) Planktonalgen','Abhandlungen der Naturwissenschaftlichen Verein zu Bremen 16: 313-398',NULL,'https://www.archive.org/download/abhandlungenhera16natu/abhandlungenhera16natu.pdf',1),(149,'LUKAS, K.J. & GOLUBIĆ, S.',1981,'New endolithic Cyanophytes from the north Atlantic Ocean: I. Cyanosaccus piriformis gen. et sp. nov.','Journal of Phycology 17(3): 224-229',NULL,'https://dx.doi.org/10.1111/j.1529-8817.1981.tb00843.x',0),(150,'LAMPRINOU, V., HERNÁNDEZ-MARINÉ, M., CANALS, T., KORMAS, K., ECONOMOU-AMILI, A. & PANTAZIDOU, A.',2011,'Morphology and molecular evaluation of Iphinoe spelaeobios gen. nov., sp. nov. and Loriellopsis cavernicola gen. nov., sp. nov., two stigonematalean cyanobacteria from Greek and Spanish caves','International Journal of Systematic and Evolutionary Microbiology 61: 2907–2915',NULL,'https://dx.doi.org/10.1099/ijs.0.029223-0',0),(151,'MARTINS, M.D., RIGONATO, J., TABOGA, S.R. & BRANCO, L.H.Z.',2016,'Proposal of Ancylothrix gen. nov., a new genus of Phormidiaceae (Cyanobacteria, Oscillatoriales) based on a polyphasic approach','International Journal of Systematic and Evolutionary Microbiology 66: 2396–2405',NULL,'https://dx.doi.org/10.1099/ijsem.0.001044',0),(152,'DADHEECH, P.K., MAHMOUD, H., KOTUT, K. & KRIENITZ, L.',2014,'Desertifilum fontinale sp. nov. (Oscillatoriales, Cyanobacteria) from a warm spring in East Africa, based on conventional and molecular studies','Fottea 14(2): 129-140',NULL,'https://dx.doi.org/10.5507/fot.2014.010',0),(153,'DADHEECH, P.K., CASAMATTA, D.A., CASPER, P. & KRIENITZ, L.',2013,'Phormidium etoshii sp. nov. (Oscillatoriales, Cyanobacteria) described from the Etosha Pan, Namibia, based on morphological, molecular and ecological features','Fottea 13(2): 235-244',NULL,'https://dx.doi.org/10.5507/fot.2013.019',0),(154,'FLORENZANO, G., SILI, C., PELOSI, E. & VINCENZINI, M.',1985,'Cyanospira rippkae and Cyanospira capsulata (gen. nov. and spp. nov.): new filamentous heterocystous cyanobacteria from Magadi lake (Kenya)','Archives of Microbiologogy 140: 301-306',NULL,'',0),(155,'MARTINS, M.D. & BRANCO, L.H.Z.',2016,'Potamolinea gen. nov. (Oscillatoriales, Cyanobacteria): a phylogenetically and ecologically coherent cyanobacterial genus','International Journal of Systematic and Evolutionary Microbiology 66(9): 3632-3641',NULL,'https://dx.doi.org/10.1099/ijsem.0.001243',0),(156,'SAW, J.H.W., SCHATZ, M., BROWN, M.V., KUNKEL, D.D., FOSTER, J.S., SHICK, H., CHRISTENSEN, S., HOU, S., WAN, X. &  DONACHIE, S.P.',2013,'Cultivation and Complete Genome Sequencing of Gloeobacter kilaueensis sp. nov., from a Lava Cave in Kīlauea Caldera, Hawai\'i','PLoS ONE 8(10): e76376',NULL,'https://doi.org/10.1371/journal.pone.0076376',0),(157,'MAREŠ, J., KOMÁREK, J., COMPERE, P. & OREN, A.',2013,'(2194) Proposal to conserve the name Gloeobacter violaceus against Aphanothece caldariorum, Gloeothece coerulea, and Gloeothece linearis (Cyanophyceae)','Taxon 62(5): 1055',NULL,'https://dx.doi.org/10.12705/625.23',0),(158,'MAREŠ, J., HROUZEK, P., KAŇA, R., VENTURA, S., STRUNECKÝ, O. & KOMÁREK, J.',2013,'The Primitive Thylakoid-Less Cyanobacterium Gloeobacter Is a Common Rock-Dwelling Organism','PLoS ONE 8(6): e66323',NULL,'https://doi.org/10.1371/journal.pone.0066323',0),(159,'HENTSCHKE, G.S., JOHANSEN, J.R., PIETRASIAK, N., FIORE, M.F., RIGONATO, J., SANT´ANNA, C.L. & KOMÁREK, J.',2016,'Phylogenetic placement of Dapisostemon gen. nov. and Streptostemon, two tropical heterocytous genera (Cyanobacteria)','Phytotaxa 245(2): 129-143',NULL,'https://dx.doi.org/10.11646/phytotaxa.245.2.4',0),(160,'SANT´ANNA, C.L., AZEVEDO, T.M.P., KAŠTOVSKÝ, J. & KOMÁREK, J.',2010,'Two form–genera of aerophytic heterocytous cyanobacteria from Brasilian rainy forest „Mata Atlântica”','Fottea 10(2): 217-228',NULL,'https://doi.org/10.5507/fot.2010.012',1),(161,'BAGCHI, S.N., DUBEY, N. & SINGH, P.',2017,'Phylogenetically distant clade of Nostoc-like taxa with the description of Aliinostoc gen. nov. and Aliinostoc morphoplasticum sp. nov.','International Journal of Systematic and Evolutionary Microbiology 67(9): 3329-3338',NULL,'https://doi.org/10.1099/ijsem.0.002112',0),(162,'CAIRES, T.A., DE MATTOS LYRA, G., HENTSCHKE, G.S., DE GUSMAO PEDRINI, A., SANT´ANNA, C.L. & DE CASTRO NUNES, J.M.',2018,'Neolyngbya gen. nov. (Cyanobacteria, Oscillatoriaceae): A new ﬁlamentous benthic marine taxon widely distributed along the Brazilian coast','Molecular Phylogenetics and Evolution 120: 196-211',NULL,'https://doi.org/10.1016/j.ympev.2017.12.009',0),(163,'GENUÁRIO, D.B., SANT ANNA, C.L. & MELO, I.S.',2018,'Elucidating the Cronbergia (cyanobacteria) dilemma with the description of Cronbergia amazonensis sp. nov. isolated from Solimões river (Amazonia, Brazil)','Algal Research 29: 233-241',NULL,'https://doi.org/10.1016/j.algal.2017.11.034',0),(164,'KOMÁREK, J., ZAPOMĚLOVÁ, E. & HINDÁK, F.',2010,'Cronbergia gen. nov., a new cyanobacterial genus (Cyanophyta) with a special strategy of heterocyte formation','Cryptogamie, Algologie 31(3) 321-341',NULL,'',0),(165,'KABIRNATAJ, S., NEMATZADEH, G.A., TALEBI, A.F., TABTABAEI, M. & SINGH, P.',2018,'Neowestiellopsis gen. nov, a new genus of true branched cyanobacteria with the description of Neowestiellopsis persica sp. nov. and Neowestiellopsis bilateralis sp. nov., isolated from Iran','Plant Systematics and Evolution 304:501–510',NULL,'https://doi.org/10.1007/s00606-017-1488-6',0),(166,'BROWN, I.I., MUMMEY, D. & COOKSEY, K.E.',2005,'A novel cyanobacterium exhibiting an elevated tolerance for iron','FEMS Microbiology Ecology 52: 307-314',NULL,'https://doi.org/10.1016/j.femsec.2004.11.020',0),(167,'LIU, Y., WANG, Z., LIN, S., YU, G. & LI, R.',2013,'Polyphasic characterization of Planktothrix spiroides sp. nov. (Oscillatoriales, Cyanobacteria), a freshwater bloom-forming alga superﬁcially resembling Arthrospira','Phycologia 52 (4): 326-332',NULL,'https://doi.org/10.2216/13–146.1',0),(168,'NGUYEN, L.T.T., CRONBERG, G., MOESTRUP, O. & DAUGBJERG, N.',2013,'Annamia toxica gen. et sp. nov. (Cyanobacteria), a freshwater cyanobacterium from Vietnam that produces microcystins: ultrastructure, toxicity and molecular phylogenetics','Phycologia 52(1): 25-36',NULL,'https://doi.org/10.2216/10-097.1',0),(169,'McGREGOR, G.B. & SENDALL, B.C.',2017,'Iningainema pulvinus gen nov., sp nov. (Cyanobacteria, Scytonemataceae) a new nodularin producer from Edgbaston Reserve, north-eastern Australia','Harmful Algae 62: 10-19',NULL,'https://dx.doi.org/10.1016/j.hal.2016.11.021',0),(170,'SHALYGIN, S., SHALYGINA, R., JOHANSEN, J.R., PIETRASIAK, N., BERRENDERO GÓMEZ, E., BOHUNICKÁ, M., MAREŠ, J., SHEIL, C.A.',2017,'Cyanomargarita gen. nov. (Nostocales, Cyanobacteria): convergent evolution resulting in a cryptic genus','Journal of Phycology 53: 762-777',NULL,'https://doi.org/10.1111/jpy.12542',0),(171,'KOMÁREK, J., GENUÁRIO, D.B., FIORE, M.F. & ELSTER, J.',2015,'Heterocytous cyanobacteria of the Ulu Peninsula, James Ross Island, Antarctica','Polar Biology 38: 475-492',NULL,'https://doi.org/10.1007/s00300-014-1609-4',0),(172,'KOMÁREK, J., NEDBALOVÁ, L. & HAUER, T.',2012,'Phylogenetic position and taxonomy of three heterocytous cyanobacteria dominating the littoral of deglaciated lakes, James Ross Island, Antarctica','Polar Biology 35: 759-774',NULL,'https://doi.org/10.1007/s00300-011-1123-x',0),(173,'JOHANSEN, J.R., OLSEN, C.E., LOWE, R.L., FUČÍKOVÁ, K. & CASAMATTA, D.',2008,'Leptolyngbya species from selected seep walls in the Great Smoky Mountains','Algological Studies 126: 21-36',NULL,'https://doi.org/10.1127/1864-1318/2008/0126-0021',0),(174,'SCIUTO, K., MOSCHIN, E. & MORO, I.',2017,'Cryptic Cyanobacterial Diversity in the Giant Cave (Trieste, Italy): The New Genus Timaviella (Leptolyngbyaceae)','Cryptogamie, Algologie 38(4):285-323',NULL,'https://doi.org/10.7872/crya/v38.iss4.2017.285',0),(175,'POPOVIĆ, S., SUBAKOV SIMIĆ, G., KORAĆ, A., GOLIĆ, I., KOMÁREK, J.',2016,'Nephrococcus serbicus, a new coccoid cyanobacterial species from Božana Cave, Serbia','Phytotaxa 289(2): 135–146',NULL,'http://dx.doi.org/10.11646/phytotaxa.289.2.3',0),(176,'VIILLANUEVA, C.D., HAŠLER, P. DVOŘÁK, P., POULÍČKOVÁ, A. & CASAMATTA, D.A.',2018,'Brasilonema lichenoides sp. nov. and Chroococcidiopsis lichenoides sp. nov. (Cyanobacteria): two novel cyanobacterial constituents isolated from a tripartite lichen of headstones','Journal of Phycology 54:224-233',NULL,'https://dx.doi.org/10.1111/jpy.12621',0),(177,'FRITSCH, F.E.',1929,'The encrusting algal communities of certainfast-flowing streams.','New Phytologists 28(3): 165-196',NULL,'',0),(178,'TURICCHIA, S., VENTURA, S., KOMÁRKOVÁ, J. & KOMÁREK, J.',2009,'Taxonomic evaluation of cyanobacterial microflora from alkaline marshes of northern Belize. 2. Diversity of oscillatorialean genera.​','Nova Hedwigia 89(1-2): 165-200',NULL,'',0),(179,'HOFFMANN L.',1985,'Quelques remarques sur la classification des Oscillatoriaceae','Cryptigamie:Algologie 6(2): 71-79',NULL,'',0),(180,'NüBEL U.,  GARCIA-PICHEL F. & MUYZER G.',2000,'The halotolerance and phylogeny of cyanobacteria with tightly coiled trichomes (<em>Spirulina </em>Turpin) and the description of <em>Halospirulina tapeticola</em> gen. nov., sp. nov.','International Journal of Systematic and Evolutionary Microbiology 50: 1265–1277',NULL,'https://dx.doi.org/10.1099/00207713-50-3-1265',0),(181,'ROLDÁN, M. RAMÍREZ, M., del CAMPO, J., HERNÁNDEZ-MARINÉ M. & KOMÁREK J.',2013,'<em>Chalicogloea cavernicola</em> gen. nov., sp. nov. (Chroococcales, Cyanobacteria), from low-light aerophytic environments: combined molecular, phenotypic and ecological criteria','International Journal of Systematic and Evolutionary Microbiology &nbsp;63: 2326–2333',NULL,'https://dx.doi.org/10.1099/ijs.0.045468-0',0),(182,'STRUNECKÝ, O., BOHUNICKÁ, M., JOHANSEN, J.R., ČAPKOVÁ, K., RAABOVÁ, L., DVOŘÁK, P. & KOMÁREK, J.',2017,'A revision of the genus Geitlerinema and a description of the genus Anagnostidinema gen. nov. (Oscillatoriophycidae, Cyanobacteria)','Fottea, 17(1): 114–126',NULL,'https://dx.doi.org/10.5507/fot.2016.025',0),(183,'MÜHLSTEINOVÁ, R., JOHANSEN, J.R., PIETRASIAK, N. & MARTIN, M.P.',2014,'Polyphasic characterization of Kastovskya adunca gen. nov. et comb. nov. (Cyanobacteria: Oscillatoriales), from desert soils of the Atacama Desert, Chile','Phytotaxa 163 (4): 216–228',NULL,'http://dx.doi.org/10.11646/phytotaxa.163.4.2',0),(184,'STRUNECKÝ, O., KOMÁREK, J. & ŠMARDA, J.',2014,'Kamptonema (Microcoleaceae, Cyanobacteria), a new genus derived from the polyphyletic Phormidium on the basis of combined molecular and cytomorphological markers','Preslia 86: 193–207',NULL,'',0),(185,'KOMÁREK, J., ZAPOMĚLOVÁ, E., ŠMARDA, J., KOPECKÝ, J., REJMÁNKOVÁ, E., WOODHOUSE, J., NEILAN, B.A. & KOMÁRKOVÁ, J.',2013,'Polyphasic evaluation of Limnoraphis robusta, a water–bloom forming cyanobacterium from Lake Atitlán, Guatemala, with a description of Limnoraphis gen. nov.','Fottea 13(1): 39–52, 2013',NULL,'https://dx.doi.org/10.5507/fot.2013.004',0),(186,'McGREGOR, G.B. & SENDALL, B.C.',2015,'Phylogeny and toxicology of &nbsp;Lyngbya wollei (Cyanobacteria, Oscillatoriales) from north-eastern Australia, with a description of Microseira gen. nov.','Journal of &nbsp;Phycology 51: 109–119&nbsp;',NULL,'DOI: 10.1111/jpy.12256',0),(187,'KOMÁRKOVÁ, J., ZAPOMĚLOVÁ, E. & KOMÁREK, J.',2013,'Chakia (cyanobacteria), a new heterocytous genus from Belizean marshes identified on the basis of the 16S rRNA gene','Fottea 13(2): 227–233',NULL,'https://dx.doi.org/10.5507/fot.2013.018',0),(188,'LAMPRINOU, V., HERNÁNDEZ-MARINÉ, M., CANALS, T.,KORMAS, K., ECONOMOU-AMILLI, E. & PANTAZIDOU, A.',2011,'Morphology and molecular evaluation of Iphinoe spelaeobios gen. nov., sp. nov. and Loriellopsis cavernicola gen. nov., sp. nov., two stigonematalean cyanobacteria from Greek and Spanish caves','International Journal of Systematic and Evolutionary Microbiology, &nbsp;61: 2907–2915',NULL,'DOI 10.1099/ijs.0.029223-0',1),(189,'LAMPRINOU,V.,  SKARAKI, K., KOTOULAS, G., ECONOMOU-AMILLI & PANTAZIDOU, A.',2012,'Toxopsis calypsus gen. nov., sp. nov. (Cyanobacteria, Nostocales) from cave ‘Francthi’, Peloponnese, Greece: a morphological and molecular evaluation','International Journal of Systematic and Evolutionary Microbiology &nbsp;62: 2870–2877',NULL,'DOI 10.1099/ijs.0.038679-0',0),(190,'LUCKING, R.,  BARRIE, F.R. & GENNEY, D.',2014,'Dictyonerna coppinsii, a new name for the European species known as Dictyonerna interrupturn (Basidiomycota: Agaricales: Hygrophoraceae) , with a validation ofits photobiont Rhizonerna (Cyanoprokaryota: Nostocales: Rhizonernataceae)','The Lichenologist 46(3): 261-267',NULL,'https://dx.doi.org/10.1017/S0024282913000352',0),(191,'WILDE, S.B., JOHANSEN, J.R., WILDE, H.D., JIANG, P., BARTELME, B.A. & HAYNIE, R.S.',2014,'Aetokthonos hydrillicola gen. et sp. nov.: Epiphytic cyanobacteria on invasive aquatic plants implicated in Avian Vacuolar Myelinopathy','Phytotaxa 181 (5): 243–260',NULL,'http://dx.doi.org/10.11646/phytotaxa.181.5.1',0),(192,'HAUER, T., BOHUNICKÁ, M. & MÜHLSTEINOVÁ, R.',2013,'Calochaete gen. nov. (Cyanobacteria, Nostocales), a new cyanobacterial type from the “páramo” zone in Costa Rica','Phytotaxa 109 (1): 36–44',NULL,'http://dx.doi.org/10.11646/phytotaxa.109.1.4',0),(193,'ZAPOMĚLOVÁ, E., SKÁCELOVÁ, O., PUMANN, P., KOPP, R. & JANEČEK, E.',2012,'Biogeographically interesting planktonic Nostocales (Cyanobacteria) in the Czech Republic and their polyphasic evaluation resulting in taxonomic revisions of Anabaena bergii Ostenfeld 1908 (Chrysosporum gen. nov.) and A. tenericaulis Nygaard 1949 (Dolichospermum tenericaule comb. nova)','Hydrobiologia &nbsp;698:353–365',NULL,'DOI 10.1007/s10750-012-1034-z',0),(194,'KAŠTOVSKÝ, J.BERRENDERO GOMEZ, E., HLADIL, J. & JOHANSEN, J.R.',2015,'Cyanocohniella calida gen. et sp. nov. (Cyanobacteria: Aphanizomenonaceae) a new cyanobacterium from the thermal springs from Karlovy Vary, Czech Republic','Phytotaxa 181 (5): 279–292',NULL,'http://dx.doi.org/10.11646/phytotaxa.181.5.3',0),(195,'KAŠTOVSKÝ, J., BERRENDERO GOMEZ, E., HLADIL, J. & JOHANSEN, J.R.',2014,'Cyanocohniella calida gen. et sp. nov. (Cyanobacteria: Aphanizomenonaceae) a new cyanobacterium from the thermal springs from Karlovy Vary, Czech Republic','Phytotaxa 181 (5): 279–292',NULL,'http://dx.doi.org/10.11646/phytotaxa.181.5.3',0),(196,'HROUZEK, P., LUKEŠOVÁ, A., MAREŠ, J. & VENTURA, S.',2013,'Description of the cyanobacterial genus Desmonostoc gen. nov. including D. muscorum comb. nov. as a distinct, phylogenetically coherent taxon related to the genus Nostoc','Fottea, Olomouc, 13(2): 201–213',NULL,'DOI: 10.5507/fot.2013.016',0),(197,'MISCOE, H.L., JOHANSEN, J.R., KOCIOLEK, J.P., LOWE, R.L., VACCARINO, M.A., PIETRASIAK N. & SHERWOOD, A.R.',2016,'The diatom flora and cyanobacteria from caves on Kauai, Hawaii. - Taxonomy, distribution, new species.','Bibliotheca Phycologica 120: 1-152',NULL,'',1),(198,'MACHADO-DE-LIMA, N.M., MARTINS, M.D. & BRANCO, L.H.Z.',2017,'Description of a tropical new species of Wilmottia (Oscillatoriales, Cyanobacteria) and considerations about the monophyly of W. murrayi','Phytotaxa 307 (1): 043–054',NULL,'https://doi.org/10.11646/phytotaxa.307.1.4',0),(199,'KOMÁREK, J. & KOMÁRKOVÁ-LEGNEROVÁ, J.',2007,'Several rare freshwater planktic cyanobacteria (Cyanoprokaryotes) from reservoirs in South America','Hoehnea 34(1): 49-58',NULL,'',0),(200,'KOMÁREK, J.',2012,'Nomenclatural changes in heterocytous Cyanoprokaryotes (Cyanobacteria, Cyanophytes)','Fottea 12(1): 141–148',NULL,'DOI: 10.5507/fot.2012.011',0),(201,'FLECHTNER, V.R., BOYER, S.L.,  JOHANSEN, J.R. &  DeNOBLE, M.L.',2002,'Spirirestis rafaelensis gen. et sp. nov. (Cyanophyceae), a new cyanobacterial genus from arid soils','Nova Hedwigia 74(1-2): &nbsp;1-24',NULL,'DOI: 10.1127/0029-5035/2002/0074-0001',0),(202,'KOMÁREK, J., KOMÁRKOVÁ, J., VENTURA, S., KOZLÍKOVÁ-ZAPOMĚLOVÁ E. & REJMÁNKOVÁ E.',2017,'Taxonomic evaluation of cyanobacterial microflora from alkaline marshes of northern Belize. 3. Diversity of heterocytous genera.','Nova Hedwigia 105(3-4): 445-486',NULL,'DOI: 10.1127/nova_hedwigia/2017/0425',1),(203,'SANT’ANNA, C.L.,  AZEVEDO M.T.P.,  FIORE M.F. , LORENZI, A.S., KAŠTOVSKÝ, J. & KOMÁREK, J.',2011,'Subgeneric diversity of Brasilonema (Cyanobacteria, Scytonemataceae)','Revista Brasileira de Botanica 34(1): 51-62',NULL,'',0),(204,'VACCARINO, M.A. & JOHANSEN, J.R.',2012,'Brasilonema angustatum sp, nov. (Nostocales), a new filamentous cyanobacterial species from the Hawaiian Islands','Journal of Phycology 48: 1178–1186',NULL,'DOI: 10.1111/j.1529-8817.2012.01203.x',0),(205,'BECERA–ABSALÓN, I,  RODARTE, B., OSORIO, K.,  ALBA-LOIS, L., SEGAL–KISCHINEVZKY, C. & MONTEJANO, G.',2013,'A &nbsp;new &nbsp;species &nbsp;of &nbsp;Brasilonema &nbsp; (Scytonemataceae, &nbsp;Cyanoprokaryota) &nbsp;from &nbsp;Tolantongo, Hidalgo, Central Mexico&nbsp;','Fottea 13(1): 25–38',NULL,'https://dx.doi.org/10.5507/fot.2013.003',0),(206,'BOURRELLY, P. & MANGUIN, É.',1952,'<em>Algues d\'eau douce de la Guadeloupe et dépendances: recueillies par la Mission P. 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Neue Formen.','Forschungsberichte aus der biologische Station Plön 12: 145–153',NULL,'',0),(209,'SMITH, G.M.',1916,'A preliminary list of algae found in Wisconsin lakes.','Transactions of Wisconsin Academy of Sciences, Arts and Letters 18: 531–565',NULL,'',0),(210,'PARAKUTTY, P.R.',1940,'The Myxophyceae of the Travancore State, India.','Proceedings of the Indian Academy of Sciences B 11: 117–124',NULL,'',0),(211,'Zukal, H.',1894,'Zur Frage über den Zellinhalt der Cyanophyceen.&nbsp;','<em>Berichte der Deutschen Botanischen Gesellschaft</em> 12: &nbsp;256-266',NULL,'',0),(212,'LUND, J.W.G.',1955,'Contributions to our knowledge of British algae. XIV. Three new species from the English Lake District.&nbsp;','<em>Hydrobiologia</em> 7: 219-228',NULL,'',0),(213,'SKUJA, H.',1956,'Taxonomische und biologische Studien über das Phytoplankton schwedischer &nbsp;Binnengewässer','Nova Acta Regiae Societatis Scientiarum Upsaliensis, Ser 4, 16 (3): 1‑404',NULL,'',0),(214,'ŠKORBATOV, L.A.',1923,'&nbsp;Myxophycearum in provincia Charkoviensi &nbsp;(Ukrainae) inventarum novae species &nbsp;et varietates. &nbsp;','Not. Syst. Inst. Cryptog. Horti Bot. 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Teil VIII ].&nbsp;','<em>Hedwigia</em> 68: &nbsp;93-114',NULL,'',0),(220,'STARMACH, K.',1957,'<em>Plectonema batrachospermum</em> sp. n.&nbsp;','<em>Acta Societatis Botanicorum Poloniae</em> 26(3): &nbsp;565-568',NULL,'',0),(221,'FRÉMY, P.',1930,'Les Myxophycées de l\'Afrique équatoriale française.&nbsp;','<em>Archives de Botanique, Mémoires</em> 3(2): &nbsp;1-508',NULL,'',0),(222,'SCHMIDLE, W.',1900,'Ueber einige von Professor Hansgirg in Ostindien gesammelte Süsswasseralgen.&nbsp;','<em>Hedwigia</em> 39: &nbsp;160-190',NULL,'',0),(223,'DIXIT, S.C:',1936,'&nbsp;The Myxophyceae of the Bombay Presidency, India &nbsp;','<em>Proceedings of the Indian Academy of Sciences </em>3(1): 93-106',NULL,'',0),(224,'GOMONT, M.',1899,'&nbsp;Sur quelques Oscillariées nouvelles','<em>Bulletin de la Société Botanique de France</em> 46: &nbsp;25-41',NULL,'',0),(225,'AN, G.S.',1992,'Validation of new species names of blue-green algae (Cyanophyta) from Korea.&nbsp;','<em>Fragmenta Floristica et Geobotanica</em> 37(2): &nbsp;417-424',NULL,'',0),(226,'ELENKIN, A.A.',1949,'<em>Monographia algarum Cyanophycearum aquidulcium &nbsp;et terrestrium in finibus URSS inventarum. Pars specialis (Syatematica), &nbsp;Fasc. II. III. Hormogoneae (Geitl.) Elenk</em>. &nbsp;pp. 985-1908, &nbsp;Mosqua &amp; Leningrad: Sumptibus Academiae Scientarum URSS.','&nbsp; Mosqua &amp; Leningrad: Sumptibus Academiae Scientarum URSS, pp. 985-1908,',NULL,'',0),(227,'SCHMIDLE, W.',1897,'Beiträge zur Algenflora des Schwarzwaldes und des Oberrheins VI','<em>Hedwigia</em> 36: &nbsp;1-25',NULL,'',0),(228,'STARMACH, K.',1963,'&nbsp;<em>Plectonema tatrica</em>, a new species of blue-green algae from the Tatra Mountains','<em>Acta Hydrobiologica</em> 10(4): &nbsp;427-434',NULL,'',0),(229,'AZEVEDO, M.T.P.',1991,'Edaphic blue-green algae from the São Paulo Botanical Garden, Brazil','<em>Algological Studies</em> 64: &nbsp;503-526',NULL,'',0),(230,'SCHWABE, G.H.',1960,'&nbsp;Zur autotrophen Vegetation in ariden Böden. Blaualgen und Lebensraum IV.&nbsp;','<em>Österreichische Botanische Zeitschrift</em> 107: &nbsp;281-309',NULL,'',0),(231,'UMEZAKI, I. & WATANABE, M.',1994,'Enumeration of the Cyanophyta &nbsp;(blue-green algae) of Japan 1. Chroococcales and Oscillatoriales','<em>Japanese Journal of Phycology</em> 42: &nbsp;175-219',NULL,'',0),(232,'LIU, Y., WANG, Z., LIN, S., YU, G. & LI, R.',2013,'Polyphasic characterization &nbsp;of <em>Planktothrix spiroides</em> sp. nov. (Oscillatoriales, Cyanobacteria), a freshwater bloom-forming alga superficially resembling <em>Arthrospira</em>. <em>Phycologia</em> 52(4): &nbsp;326-332','<em>Phycologia</em> 52(4): &nbsp;326-332',NULL,'',1),(233,'WOLOSZINSKA, J.',1913,'&nbsp;Das &nbsp;Phytoplankton einiger javanischer Seen mit Berücksichtigung des Sawa- Planktons.','Bulletin International de l\'Académie des Sciences de Cracovie. Classe &nbsp;des Sciences Mathématiques et Naturelles. Série B: Sciences Naturelles 1912: &nbsp;649-709.',NULL,'',0),(234,'UTERMöHL, H.',1925,'Limnologische Phytoplanktonstudien. Die Besiedelung &nbsp;ostholsteinischer Seen mit Schwebpflanzen: Mit 42 Textabbildungen und &nbsp;Kurventafel.&nbsp;','<em>Archiv für Hydrobiologie Supplement</em> 5: &nbsp;1-527.',NULL,'',0),(235,'GOMONT, M.',1892,'Monographie des Oscillariées (Nostocacées Homocystées) deuxiéme partie -Lyngbyées','<em>Annales des Sciences Naturelles, Botanique, Série 7,</em> 16: &nbsp;91-264',NULL,'',0),(236,'FARIDI, M..F. & KHALIL, Z.',1974,'A new species of <em>Oscillatoria</em> (Cyanophyceae) Pakistan.&nbsp;','<em>Biologia (Pakistan)</em> 20(1): &nbsp;65-??.',NULL,'',0),(237,'KLEBAHN, H.',1895,'Gasvacuolen, ein Bestandteil der Zellen der wasserblütebildenden Phycochromaceen.','<em>Flora</em> 80: &nbsp;241-282',NULL,'',0),(238,'SKUJA, H.',1948,'Taxonomie des Phytoplanktons einiger Seen in Uppland, Schweden','Symbolae Botanicae Upsalienses 9(3): 1–399',NULL,'',0),(239,'NYGAARD, G.',1926,'Plankton from two lakes of the Malayan region.&nbsp;','<em>Videnskabelige Meddelelser Dansk Naturhistorisk Forening</em> 82: &nbsp;197-240',NULL,'',0),(240,'GONZALVES, E.A. & KAMAT, N.D.',1959,'Two new species of Anabaena from Western India','Hydrobiologia 13(3): 236–238',NULL,'',0),(241,'LAMMERMANN, E.',1906,'Über die von Herrn Dr. Walter Volz auf seiner Weltreise gesammelte Süsswasseralgen','<em>Abhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen</em> 18(1): 143–174',NULL,'',0),(242,'LEMMERMANN, E.',1906,'Über die von Herrn Dr. Walter Volz auf seiner Weltreise gesammelten Süsswasseralgen.&nbsp;','<em>Abhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen</em> 18(1): &nbsp;143-174',NULL,'',0),(243,'ANTARIKANONDA, P.',1985,'A new species of the genus Anabaena: Anabaena siamensis sp. nov. (Cyanophyceae) from Thailand.','Nova Hedwigia 41:343-352',NULL,'',0),(244,'CRONBERG, G.',2003,'New and interesting cyanoprokaryotes from temperate, brackish ponds and Baltic Sea','Algological Studies 109: 197-211',NULL,'',0),(245,'LEMMERMANN, E.',1898,'Beitrag zur Algenflora von Schlesien.','<em>Abhandlungen Naturwissenschaftlicher Verein Bremen</em> 14:&nbsp; 1-520',NULL,'',0),(246,'WATANABE, M.',2003,'Studies on planktonic blue-green algae 9. <em>Anabaena akankoensis</em> sp. nov. from Lake Akan, Hokkaido','<em>Bulletin of the National Science Museum Series B (Botany)</em> 29(1): &nbsp;9-13',NULL,'',0),(247,'KISELEV, I.A.',1932,'Materiali po mikroflore jugo-vostocknoi Chasti Morja Laptevykh. &nbsp;(Beitrage zur Mikroflora des sud-ostlichen Teiles des Lapter-Meeres).','Gosudarstveniy Gydrologicheskii Institut Issledovaniya morei S.S.S.R 15: 66-104',NULL,'',0),(248,'CRONBERG, G. & KOMÁREK, J.',2004,'Some nostocalean Cyanoprokaryotes from lentic habitats of Eastern and Southern Africa','Nova Hedwigia 78(1-2): 71-106',NULL,'',0),(249,'WELSH, H.',1961,'A new species of <em>Hydrocoryne </em>Schwabe and <em>Anabaena </em>Bory','Revista Biologia 2(3-4): 257-260',NULL,'',0),(250,'WATANABE, M,',1992,'Studies on the planktonic blue-green algae. 4. Some <em>Anabaena</em> species with straight trichomes in Japan','<em>Bulletin</em> of the National <em>Science Museum</em>, Series <em>B</em> 18(4): 123-137',NULL,'',0),(251,'NYGAARD, G.',1949,'Hydrobiological studies on some Dannish ponds and lakes.','Kongelige Danske Videnskabernes <em>Selskab</em>,  Biologiske <em>skrifter</em>, 7(1): 1-293',NULL,'',0),(252,'LEMMERMANN, E.',1898,'Beiträge zur Kenntniss der Planktonalgen. II. Beschreibung neuer Formen<em></em>','<em>Botanisches Centralblatt</em> 76: &nbsp;150-156',NULL,'',0),(253,'HILL, H.',1976,'&nbsp;A new species of <em>Anabaena</em> (Cyanophyta, Nostocaceae) from a Minnesota lake. I.&nbsp;','<em>Phycologia</em> 15: &nbsp;61-64',NULL,'',0),(254,'KOMÁREK, J. & KOMÁRKOVÁ-LEGNEROVÁ, J.',2002,'Contribution to the &nbsp;knowledge of natural populations of planktic cyanoprokaryotes &nbsp;from central Mexico','Preslia 74: 207-233',NULL,'',0),(255,'CRONBERG, G. & KOMÁRKOVÁ, J.',1988,'&nbsp;<em>Anabaena farciminiformis</em>, a new nostocacean blue-green alga from Scania, South Sweden','Algological Studies 50-53: 277-282&nbsp;',NULL,'',0),(256,'BERNARD, C.',1908,'<em>Protococcacées et desmidiées d\'eau douce, récoltées à Java</em>. &nbsp;','Batavia: Landsdrukkerij, pp. 1-230',NULL,'',0),(257,'PANKOW, H.',1965,'Bemerkungen zur Systematik der <em>Anabaena</em>-formen mit spiralig, schraubig oder kreisförming gewundenen Trichomen','Limnologica 3(2): 163-172&nbsp;',NULL,'',0),(258,'TRELEASE, W.',1889,'The \'working\' of the Madison Lakes.&nbsp;','<em>Transactions of the Wisconsin Academy of Sciences, Arts, and Letters</em> 7: &nbsp;121-129',NULL,'',0),(259,'KOMÁRKOVÁ-LEGNEROVÁ, J. & ELORANTA, P.',1992,'Planktic blue-green algae (Cyanophyta) from Central Finland (Jyväskylä region) with special reference to the genus <em>Anabaena</em>.','Algological Studies 67: 103-133&nbsp;',NULL,'',0),(260,'VASISHTA, P.C.',1960,'<em>Anabaena nathii</em> sp. nov. from Hoshiarpur.','Ress. 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B</em> 22(3): &nbsp;93-97',NULL,'',0),(264,'KOMÁREK, J. & ETTL, H.',1958,'Algologische Studien','Verlag der Tschechoslowakischen Akademie der Wisseschaft, Prag, 1-358',NULL,'',0),(265,'KOMÁREK, J.',1984,'Sobre las cyanofíceas de Cuba: (3) Especies &nbsp;planctónicas que forman florecimientos de las aguas. - Acta &nbsp;Bot. Cubana, La Habana, 19: 33','Acta &nbsp;Botanica Cubana &nbsp;19: 1-33',NULL,'',0),(266,'DENIS, M. & FRÉMY, P.',1924,'Une nouvelle Cyanophycées hétérocystée: <em>Anabaena viguieri</em>.&nbsp;','<em>Bulletin de la Société Linnéenne de Normandie, série 6</em> 7: &nbsp;122-125',NULL,'',0),(267,'KOMÁREK J. & CRONBERG G.',2001,'Some chroococcalean and oscillatorialean Cyanoprokaryotes from southern African lakes, ponds and pools.','Nova Hedwigia 73(1-2): 129-160',NULL,'',0),(268,'AZEVEDO, M.T.P., SANT\'ANNA, C.L., SENNA, P.A.C., KOMÁREK, J. & KOMÁRKOVÁ, J.',2003,'Contribution to the microflora of chroococcalean cyanoprokaryotes in São Paulo State, Southeast Brazil.','Hoehnea 30(3): 285-295',NULL,'',0),(269,'WEST W. & WEST G.S:',1906,'A comparative study of the plankton of some Irish lakes','<em>Transactions of the Royal Irish Academy33 B: &nbsp;77-116</em>',NULL,'',0),(270,'THU N.K., TANABE Y., YOSHIDA M., MATSUURA H. & WATANABE M.M.',2012,'<em>Aerosakkonema funiforme</em> gen. et sp. nov. (Oscillatoriales), a new gas-vacuolated oscillatorioid cyanobacterium isolated from a mesotrophic reservoir.','Phycologia 51(6): 672-683',NULL,'https://dx.doi.org/10.2216/11-130.1',0),(271,'WEST W',1912,'Fresh-water algae &nbsp;with a supplement of marine diatoms','<em>Proceedings of the Royal Irish Academy</em> 31(16): &nbsp;1-62',NULL,'',0),(272,'KOMÁRKOVÁ-LEGNEROVÁ J. & CRONBERG G.',1994,'Planktic blue-green alage from lakes in South Scania, Sweden. Part I. 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Mit den &nbsp;opiz-preise Gekrönte Arbeit auf Kosten des Opizfondes.','<em>Archiv für die naturwissenschaftliche Landesdurchforschung von Böhmen</em> 8(4): &nbsp;1-268.',NULL,'',0),(276,'BECERRA-ABSALÓN, I., JOHANSEN, J.R., MUNOZ-MARTÍN, M.A. & MONTEJANO, G.',2018,'<em>Chroakolemma</em> gen. nov. (Leptolyngbyaceae, Cyanobacteria) from soil biocrusts in the semi-desert Central Region of Mexico','<em>Phytotaxa</em> 367(3): &nbsp;201-218',NULL,'https://doi.org/10.11646/phytotaxa.367.3.1',0),(277,'KILGORE, CH., JOHANSEN, J.R., MAI, T., HAUER, T., CASAMATTA, D.A. & SHEIL, C.A.',2018,'Molecular characterization of Geitleria appalachiana sp. nov. (Nostocales, Cyanobacteria) and formation of Geitleriaceae fam. nov.','FOTTEA 18(2): 150-163',NULL,'http://dx.doi.org/10.5507/fot.2018.002',0),(278,'GUIRY, M.D., JOHANSEN, J.R. & MAI, T.',2018,'Trichocolea Dumortier, 1822, nom. et orth. cons. (Jungermanniales, Bryophyta) vs Trichocoleus Anagnostidis, 2001 (Synechococcales, Cyanophyta) and Trichocolaceae H.Nakai vs Trichocolaceae T.Mai &amp; J.R.Johansen','Notulae algarum 72:1-2',NULL,'http://www.notulaealgarum.com/documents/Notulae%20algarum%20No.%2072.pdf',0),(279,'SANT\'ANNA, C.L.,  GAMA, W.A., RIGONATO, J.,  CORREA, G., MESQUITA, M.C.B. & MARINHO, M.M.',2019,'Phylogenetic connection among close genera of Aphanizomenonaceae (Cyanobacteria): <em>Amphiheterocytum</em> gen. nov., <em>Cylindrospermopsis</em> and <em>Sphaerospermopsis</em>','Algal Research 37: 205-214',NULL,'https://doi.org/10.1016/j.algal.2018.11.026',0),(280,'GEITLER, L.',1956,'<em>Oscillatoria carotinosa</em> n. sp. and <em>O. pseudoacutissima</em> n. sp., zwei Arten mit lokalisierter Karotinoidbildung.&nbsp;','<em>Österreichische Botanische Zeitschrift</em> 103: &nbsp;342-345',NULL,'',0),(281,'KUFFERATH, H.',1914,'Contribution à l\'étude de la flore algologique du Luxembourg &nbsp;meridionale. II. Chlorophycees (exclus. Desmidiacées), Flagellates et &nbsp;Cyanophycées','Annales de Biologie Lacustre 7: &nbsp;231-271',NULL,'',0),(282,'WEST, W. & WEST, G.S.',1911,'Part VII. Freshwater Algae','In: British Antarctic Expedition 1907–09. &nbsp;Vol. 1: &nbsp;Biology, p. 263–298 &nbsp;(Ed. J. Murray)',NULL,'',0),(283,'SKUJA, H.',1937,'Süsswasseralgen aus Griechenland und Kleinasien','Hedwigia 77: 15–70',NULL,'',0),(284,'CAMPBELL, S.E. & GOLUBIĆ, S.',1985,'Benthic cyanophytes (cyanobacteria) of Solar Lake (Sinai).','Algological STudies 38/39: 311-329',NULL,'',0),(285,'WOLOSZYNSKA, J.',1913,'&nbsp;Das &nbsp;Phytoplankton einiger javanischer Seen mit Berücksichtigung des Sawa- Planktons.','',NULL,'',1),(286,'ENGENE, N., TRONHOLM, A., SALVADOR-REYES, L.A., LUESCH, H. & PAUL, V.J.',2015,'<em>Caldora penicillata</em> gen nov., sp. nov. 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V. &amp; JEEJI BAI, N.(eds): Spirulina. ETTA National<br>Symposium MCRC, Madras, pp. 12–21',NULL,'',0),(312,'GARDNER N.L.',1917,'New Pacific coast marine algae','Univ. Calif. Publ. Bot. 6: 377–416',NULL,'',0),(313,'NÜBEL, U., GARCOA-PICHEL, F. & MUYZER, G',2000,'The halotolerance and phylogeny of cyanobacteria with tightly coiled trichomes (Spirulina Turpin) and the description of <em>Halospirulina tapeticola</em> gen. nov., sp. nov.','IJSEM 50: 1265-1277',NULL,'https://dx.doi.org/10.1099/00207713-50-3-1265',1),(314,'RüTZLER, K., SANTAVY, D.L. & ANTONIUS, A.',1983,'The black band disease of Atlantic reef corals: III. Distribution, ecology and development.','Marine Ecology - Pubblicazioni Della Stazione Zoologica Di Napoli I: Marine Ecology 4: 29–358.',NULL,'',0),(315,'ZIMBA, P.V., HUANG, I.S., FOLEY, J.E. & LINTON, E.W.',2017,'Identification of a new-to-science cyanobacterium, Toxifilum mysidocida gen. nov. &amp; sp. nov. (Cyanobacteria, Cyanophyceae)','Journal of Phycology 53(1): 188-197',NULL,'DOI: 10.1111/jpy.12490',0),(316,'MARTINS, M.D. & BRANCO, L.H.Z.',2016,'<em>Potamolinea </em>gen. nov. (Oscillatoriales, Cyanobacteria): a phylogenetically and ecologically coherent cyanobacterial genus','International Journal of Systematic and Evolutionary Microbiology 66(9): 3632-3641',NULL,'DOI 10.1099/ijsem.0.001243',1),(317,'MÜHLSTEINOVÁ, R. & GUIRY, M.',2018,'Seeking the true Oscillatoria: corrected epitypification of O. princeps Vaucher ex Gomont (Oscillatoriaceae, Cyanobacteria)&nbsp;','Notulae algarum No. 83',NULL,'http://www.notulaealgarum.com/documents/Notulae%20algarum%20No.%2083.pdf',0),(318,'SENDALL, B.C. &  McGREGOR, G.B.',2018,'Cryptic diversity within the Scytonema complex: Characterization of the paralytic shellfish toxin producer Heterosyctonema crispum, and the establishment of the family Heteroscytonemataceae (Cyanobacteria/Nostocales)','HArmful ALgae 80: 158-170',NULL,'https://doi.org/10.1016/j.hal.2018.11.002',0),(319,'ZHOU, W.-G., DING, D.-W., YANG, Q.-S., AHMAD, M., ZHANG, Y.-Z., LIN, X.-CH., ZHANG, Y.-Y., LING, J. & DONG, J.-D.',2018,'Marileptolyngbya sina gen. nov., sp. nov. and Salileptolyngbya diazotrophicum gen. nov., sp. nov. (Synechococcales, Cyanobacteria), species of cyanobacteria isolated from a marine ecosystem','Phytotaxa 383(1): 75-92',NULL,'https://doi.org/10.11646/phytotaxa.383.1.4',0),(320,'CAIRES, T.A., LYRA, G.M., HENTSCHKE, G.S., da SILVA, A.M.S., de ARAÚJO, V.L:,  SANT’ANNA, C.L. &  NUNES, J.M.C.',2018,'Polyphasic delimitation of a filamentous marine genus, <em>Capillus</em> gen. nov. (Cyanobacteria, Oscillatoriaceae) with the description of two Brazilian species','Algae 33(4): 291-304',NULL,'https://doi.org/10.4490/algae.2018.33.11.25',0),(321,'KOMÁREK, J.',1989,'Studies on the Cyanophytes of Cuba 7-9 &nbsp;','Folia Geobot. Phytotax., Praha, 24: 171-206',NULL,'',0),(322,'McGREGOR, G.B. & SENDALL, B.C.',2019,'<em>Potamosiphon australiensis</em> gen. nov., sp nov. (Oscillatoriales), a new filamentous cyanobacterium from subtropical north-eastern Australia','Phytotaxa 387(2): 77-93',NULL,'http://dx.doi.org/10.11646/phytotaxa.387.2.1',0),(323,'MARTINS, M.D., MACHADO-DE-LIMA, N.M. & BRANCO, L.H.Z',2018,'Polyphasic approach using multilocus analyses supports the establishment of the new aerophytic cyanobacterial genus Pycnacronema (Coleofasciculaceae, Oscillatoriales)','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.12805',1),(324,'CAIRES, T.A., LYRA, G.M., HENTSCHE, G.S., SILVA, A.M.S, ARAÚJO, V.L., SANT´ANNA, C.L. & NUNES, J.M.C.',2018,'Polyphasic delimitation of a filamentous marine genus, Capillus gen. nov. (Cyanobacteria, Oscillatoriaceae) with the description of two Brazilian species','Algae 33(4): 291-304',NULL,'https://doi.org/10.4490/algae.2018.33.11.25',1),(325,'GENUÁRIO, D.B., DE SOUZA, W.R., MONTEIRO, R.T.R., SANT´ANNA, C.L. & MELO, I.S.',2018,'Amazoninema gen. nov., (Synechococcales, Pseudanabaenaceae) a novel cyanobacteria genus from Brazilian Amazonian rivers','International Journal of Systematic and Evolutionary Microbiology 68: 2249-2257',NULL,'https://dx.doi.org/10.1099/ijsem.0.002821',0),(326,'VILLANUEVA, CH.D., GARVEY, A.D., HAŠLER, P., DVOŘÁK, P., POULÍČKOVÁ, A., NORWICH, A.R. & CASAMATTA D.A.',2019,'Descriptions of <em>Brasilonema geniculatum</em> and <em>Calothrix dumus</em> (Nostocales, Cyanobacteria): two new taxa isolated from cemetery tombstones','Phytotaxa 387(1): 1-20',NULL,'https://doi.org/10.11646/phytotaxa.387.1.1',0),(327,'WOLOSZYNSKA, J.',1911,'Przycynek do znajomosci glonów planktonowych [Beitrag zur Kenntnis der Planktonalgen]','Bulletin International de l\'Académie des Sciences de Cracovie. Classe &nbsp;des &nbsp;Sciences Mathématiques et Naturelles. Série B: Sciences Naturelles 1911: 529-530',NULL,'',0),(328,'UTERMÖHL, H.',1925,'Limnologische Phytoplanktostudien. Die Besiedlung ostholsteinnischer Seen mit Schwebpflanzen.','Archiv für Hydrobiologie, Supplement 5: 1-527',NULL,'',0),(329,'VAN GOOR, A.C.J.',1918,'Zur Kenntnis der Oscillatoriaceeen','&nbsp;Recueil des Travaux Botaniques Neerlandais 15: 256-263',NULL,'',0),(330,'DVOŘÁK, P., HAŠLER, P., PITELKOVÁ P., TABÁKOVÁ, P., CASAMATTA, D.A. & POULÍČKOVÁ, A.',2017,'A new cyanobacterium from the Everglades, Florida – Chamaethrixgen. nov.','Fottea 17(2): 269-276',NULL,'https://dx.doi.org/10.5507/fot.2017.017',0),(331,'GONZÁLEZ-RESENDIZ, L., JOHANSEN, J.R., ESCOBAR-SÁNCHEZ, V., SEGAL-KISCHINEVZKY, C., JIMÉNEZ-GARCÍA, L. & LEÓN-TEJERA, H.',2018,'Two new species of Phyllonema (Rivulariaceae, Cyanobacteria) with an emendation of the genus','Journal of Phycology 54: 638-652',NULL,'https://dx.doi.org/10.1111/jpy.12769',0),(332,'ALVARENGA, D.O., RIGONATO, J., BRANCO, L.H.Z., MELO, I.S. & FIORE, M.F.',2016,'<em>Phyllonema aviceniicola</em> gen. nov., sp. nov. and <em>Foliisarcina bertiogensis</em> gen. nov., sp. nov., epiphyllic cyanobacteria associated with <em>Avicennia schaueriana</em> leaves','International Journal of Systematic and Evolutionary Microbiology 66: 689-700',NULL,'https://dx.doi.org/10.1099/ijsem.0.000774',0),(333,'CAI, F., YANG, Y., WEN, Q. & LI, R.',2018,'Desmonostoc danxiaense sp. nov. (Nostocales, Cyanobacteria) from Danxia mountain in China based on polyphasic approach','Phytotaxa 367(3): 233-244',NULL,'https://doi.org/10.11646/phytotaxa.367.3.3',0),(334,'STRUNECKÝ, O., KOMÁREK, J., JOHANSEN, J.R. , LUKEŠOVÁ, A. & ELSTER, J.',2013,'Molecular and morphological criteria for revision of the genus <em>Microcoleus </em>(Oscillatoriales, Cyanobacteria)','Journal of Phycology 49: 1167-1180',NULL,'https://dx.doi.org/10.1111/jpy.12128',0),(335,'HEIDARI, F., ZIMA, J. jr., RIAHI, H. & HAUER, T.',2018,'New simple trichal cyanobacterial taxa isolated from radioactive thermal springs','Fottea 18(2): 137-149',NULL,'https://dx.doi.org/10.5507/fot.2017.024',0),(336,'CASAMATTA, D.A., JOHANSEN, J.R, VIS, M.L. & BROADWATER, S.T.',2005,'Molecular and morphological characterization of ten polar and near-polar strains within the Oscillatoriales (Cyanobacteria)','Journal of Phycology 41: 421-438',NULL,'https://doi.org/10.1111/j.1529-8817.2005.04062.x',1),(337,'BERRENDERO GÓMEZ, E.B., JOHANSEN, J.R., KAŠTOVSKÝ, J., BOHUNICKÁ, M. & ČAPKOVÁ, K.',2016,'<em>Macrochaete</em> gen. nov. (Nostocales, Cyanobacteria), a taxon morphologically and molecularly distinct from <em>Calothrix</em>','Journal of Phycology 52(4): &nbsp;638-655',NULL,'https://doi.org/10.1111/jpy.12425',0),(338,'CHAKRABORTY, S., MARUTHANAYAGAM, V., ACHARI, A., MAHANSARIA, R., PRAMANIK, A., JAISANKAR, P. & MUKHERJEE, J.',2018,'<em>Oxynema aestuarii </em>sp. nov. 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Plantes cellulaires et vasculaires. 262 pp','Paris,Friedrich Klincksieck&nbsp;',NULL,'',0),(343,'AGARDH, C.A.',1827,'Aufzählung einiger in den östreichischen Ländern gefundenen neuen &nbsp;Gattungen und Arten von Algen, nebst ihrer Diagnostik und beigefügten &nbsp;Bemerkungen','Flora oder Botanische Zeitung &nbsp;10 (40): 625-640',NULL,'',0),(344,'SKUJA, H.',1949,'Zur Süsswasseralgen-flora Burmas','Nova Acta Regiae Societatis Scientiarum Upsaliensis, Series 4 14(5): &nbsp;1-188',NULL,'',0),(345,'OSTENFELD C.H.',1908,'The Phytoplankton of the Aral Sea and its Affluents','In: Berg L.S. (ed.), Scientific Results of the Aral Sea Expedition 8: 123-225',NULL,'',0),(346,'FORTI, A.',1911,'Diagnoses myxophycearum novarum','Atti e Memorie dell\'Accademia di Agricoltura, Scienze e Lettere, Arti e Commercia di Verona, Series IV, 12: 1-5',NULL,'',0),(347,'KISELEV, I.A.',1927,'&nbsp;Zur Kenntnis des Algen des Aralsees [Novye dannye o vodoroslyakh Aralskogo morya.]','Bull. Sect. Ichthyol. appl. 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A.',1965,'Thermal algae of Western India - I. Algae of the hot spring at Akloli and Ganesh Puri','Hydrobiologia 25(3-4): 330-340',NULL,'',0),(382,'ČADO, I.',1958,'Sostav i zonal\'nost\' mikrofitov pribrežnych skal Ochridskogo ezera','Zbornik rabotite filos. fak. univ. Skopje, Hydrobiološki zavod Ochrid <strong>5</strong>(21): 1‑43',NULL,'',0),(383,'WEST, G.S.',1904,'West Indian freshwater algae','Journal of Botany 42:&nbsp; 281-294',NULL,'',0),(384,'FRITSCH, F.E.',1912,'&nbsp;Freshwater algae.','In: <em>National Antarctic Expedition 1901-1904 Natural History. Vol. VI. Zoology and Botany [Part 3]</em>. (Anon. Eds), pp. 1-66',NULL,'',0),(385,'SAUVAGEAU, M.',1892,'Sur les algues d\'eau douce recoltées en Algérie pendant le session de la Societé Botanique en 1892.','<em>Bulletin de la Société Botanique de France</em> 39',NULL,'',0),(386,'CHU, H.-J.',1952,'Some New Myxophyceae from Szechwan Province, China','The Ohio Journal of Science 52 (2): 96-101',NULL,'',0),(387,'FRITSCH, F.E. & RICH, I.',1929,'&nbsp;Freshwater algae from Grigualand West','Transactions of the Royal Society of South Africa 18: 91-92&nbsp;',NULL,'',0),(388,'VORONICHIN, N.N.',1923,'Novye vidy &nbsp;vodoroslej s Kavkaza I','Botaničeskie Materialy &nbsp;Instituta Sporovykh Rastenij Glavnogo Botanicheskogo Sada R.S.F.S.R. <strong>2</strong>(7): 97-112',NULL,'',0),(389,'GEITLER, L.',1933,'Diagnosen neuer Blaualgen von den Sunda-Inseln','Archiv für Hydrobiologie, Suppl. 12: 622-634',NULL,'',0),(390,'SARAF, A.G., DAWDA, H.G. & SINGH, P.',2019,'<em>Desikacharya </em>gen. nov., a phylogenetically distinct genus of Cyanobacteria along with the description of two new species, <em>Desikacharya nostocoides</em> sp. nov. and <em>Desikacharya </em>soli sp. nov., and reclassification of <em>Nostoc thermotolerans</em> to <em>Desikacharya thermotolerans</em> comb. nov.','International Journal of Systemetic and Evolutionary Microbiology 69(2): 307-315',NULL,'https://dx.doi.org/10.1099/ijsem.0.003093',0),(391,'SURADKAR, A., VILLANUEVA, C., GAYSINA, L.A., CASAMATTA, D.A., SARAF, A., DIGHE, G. MERGU, R. & SINGH, P.',2017,'Nostoc thermotolerans sp. nov., a soil dwelling species of Nostoc (Cyanobacteria) isolated from Madhya Pradesh, India','International Journal of Systematic and Evolutionary Microbiology 67: 1296-1305',NULL,'https://dx.doi.org/10.1099/ijsem.0.001800',0),(392,'BORZÍ, A.',1892,'Alghe d\'acqua dolce della Papuasia raccolte su cranii umani dissepolti','Nuova Notarisia 3: 35-53',NULL,'',0),(393,'LINDSTEDT, A.',1943,'Die Flora der marinen Cyanophyceen der schwedischen Westküste','Lund: Håkan Ohlssons Buchdruckerei, 121 pp.',NULL,'',0),(394,'GAMA, W.A., RIGONATO, J., FIORE, M.F. & SANT´ANNA, C.L.',2019,'New insights into <em>Chroococcus </em>(Cyanobacteria) and two related genera: <em>Cryptococcum </em>gen. nov. and <em>Inacoccus</em> gen. nov.','European Journal of Phycology',NULL,'https://doi.org/10.1080/09670262.2018.1563913',0),(395,'HOWE, M.A:',1918,'The marine algae and marine spermatophytes of the Tomas Barrera Expedition to Cuba','<em>Smithsonian Miscellaneous Collections</em> 68(11): 1-13',NULL,'',0),(396,'ZHANG, Q., ZHENG, L., LI, T., LI, R. & SONG., L',2019,'Aliterella shaanxiensis (Aliterellaceae), a new coccoid cyanobacterial species from China','Phytotaxa 374(3): 211-220',NULL,'https://doi.org/10.11646/phytotaxa.374.3.2',0),(397,'MAREŠ, J., JOHANSEN, J.R., HAUER, T., ZIMA, J. Jr., VENTIRA, S., CUZMAN, O., TIRIBILLI, B. & KAŠTOVSKÝ, J.',2019,'Taxonomic resolution on the genus Cyanothece (Chroococcales, Cyanobacteria), with a treatment on Gloeothece and three new genera, Croccosphaera, Rippkaea, and Zehria','Journal of Phycology 55: 578-610',NULL,'https://dx.doi.org/10.1111/jpy.12853',0),(398,'SHALYGIN, S., HUANG, I.-S., ALLEN, E.H., BURKHOLDER, J.M. & ZIMBA, P.V.',2019,'Odorella benthonica gen. &amp; sp. nov. (Pleurocapsales, Cyanobacteria): An odor and prolific toxin producer isolated from a California aqueduct','Journal of Phycology 55: 509-520',NULL,'https://dx.doi.org/10.1111/jpy.12834',0),(399,'SANT´ANNA, C.L., GAMA, W.A., SILVA, T.G. & VIEIRA, A.A.H.',2018,'A new species of Trichodesmium (Cyanobacteria) from freshwaters, Brazil','Rodriguésia 69(4): 2019-2024',NULL,'https://dx.doi.org/10.1590/2175-7860201869433',0),(400,'CELLAMARE, M., DUVAL, C., DRELIN, Y., DJEDIAT, C., TOUIBI, N., AGOGUÉ, H., LEBOULANGER, C., ADER, M. & BERNARD, C.',2018,'Characterization of phototrophic microorganisms and description of new cyanobacteria isolated from the saline-alkaline crater-lake Dziani Dzaha (Mayotte, Indian Ocean)','FEMS Microbiology Ecology, 94 (8): fiy108',NULL,'https://doi.org/10.1093/femsec/fiy108',0),(401,'CAI, F., LI, X., YANG, Y., JIA, N., HUO, D. & LI., R.',2019,'Compactonostoc shennongjiaensis gen. &amp; sp. nov. (Nostocales, Cyanobacteria) from a wet rocky wall in China','Phycologia',NULL,'https://doi.org/10.1080/00318884.2018.1541270',0),(402,'CAI, F., LI, X., GENG, R., PENG, Z., & LI, R.',2019,'Phylogenetically distant clade of Nostoc–like taxa with the description of Minunostoc gen. nov. and Minunostoc cylindricum sp. nov.','Fottea 19(1): 13-24',NULL,'https://dx.doi.org/10.5507/fot.2018.013',0),(403,'AKAGHA, S.C., JOHANSEN, J.R., NWANKWO, D.I. & YIN, K.',2019,'Lagosinema tenuis gen. et sp. nov. (Prochlorotrichaceae, Cyanobacteria): a new brackish water genus from Tropical Africa','Fottea 19(1): 1-12',NULL,'https://dx.doi.org/10.5507/fot.2018.012',0),(404,'PIETRASIAK, N., OSORIO-SANTOS, K., SHALYGIN, S., MARTIN, M.P. & JOHANSEN, J.R.',2019,'When is a lineage a species? A case study in Myxacorys gen. nov. (Synechococcales: Cyanobacteria) with the description of two new species from the Americas','Journal of Phycology 55: 976-996',NULL,'https://dx.doi.org/10.1111/jpy.12897',0),(405,'KONSTANTINOU, D., VOULTSIADOU, E., ZERVOU, S.-K., HISKIA, A. & GKELIS, S.',2019,'Leptohoe, a new genus of marine Cyanobacteria (Synechococcales) and three new species associated with sponges from the Aegean Sea','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.12866',0),(406,'GARDNER, N.L.',1918,'New Pacific coast marine algae III','University of California Publications in Botany 6(17): &nbsp;455-486',NULL,'',0),(407,'Campbell, S.E.',1985,'\'Oscillatoria limnetica\' from Solar Lake, Sinai, is a Phormidium (Cyanophyta or Cyanobacteria)','Algological Studies 38-39: 175-190',NULL,'',0),(408,'DEBNATH, M.,  SINGH, T. &  BHADURY, P.',2017,'New records of Cyanobacterial morphotypes with <em>Leptolyngbya indica</em> sp. nov. from terrestrial biofilms of the Lower Gangetic Plain, India','Phytotaxa 316 (2): 101–120',NULL,'https://doi.org/10.11646/phytotaxa.316.2.1',1),(409,'Claus G.',1962,'Data on the ecology of the algae of Peace Cave in Hungary','Nova Hedwigia 4: 55-79',NULL,'',0),(410,'SCHMIDT, G.',1914,'Zur Kenntnis einiger Oscillariaceen.&nbsp;','Berichte der Deutschen Botanischen Gesellschaft 32(2): 122-130&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;',NULL,'',0),(411,'KUFFERATH, H.',1929,'Algues et protistes muscicoles, corticoles et terrestres récoltés sur la montagne de Barba (Costa Rica)','Annales de Cryptogamie Exotique 2: 23-52',NULL,'',0),(412,'GARDNER, N.L.',1932,'The Myxophyceae of Porto Rico and the Virgin Islands','&nbsp;In: Scientific Survey of Porto Rico and the Virgin Islands. Volume VIII. Part 2. (Anon. Eds), pp. 249-311',NULL,'',0),(413,'LEMMERMANN, E.',1904,'Das Plankton schwedischer Gewässer','Arkiv för Botanik 2(2): &nbsp;1<em>-209.</em>',NULL,'',0),(414,'SARAF, A.G., DAWDA G.H. & SINGH, P.',2019,'Validation of the genus Desikacharya gen. nov. (Nostocaceae, Cyanobacteria) and three included species.','Notulae algarum 2019: 107',NULL,'http://www.notulaealgarum.com/documents/Notulae%20Algarum%20No.%20107.pdf',0),(415,'SONG, G.-F., XIANG, X.-F., WANG, Z.-J., LI, R.-H.',2015,'Polyphasic characterization of Stigonema dinghuense, sp. nov. (Cyanophyceae, Nostocophycidae, Stigonemaceae), from Dinghu Mountain, south China','Phytotaxa 213(3): 212-224',NULL,'http://dx.doi.org/10.11646/phytotaxa.213.3.2',0),(416,'JAO C.-C.',1948,'The marine Myxophyceae in the vicinity of Friday Harbor, Washington','Botanical Bulletin of Academia Sinica 2: &nbsp;161-177',NULL,'',0),(417,'SIMMER, H.',1901,'Vierter Bericht über der Kryptogamenflora der kreuzeckgruppe in Kärnten','Allgemeine botanische Zeitschrift für Systematik, Floristik, Pflanzengeographie 7(5): 83-86',NULL,'',0),(418,'WEST, G.S.',1902,'On some algae from hot springs','.Journal of Botany, British and Foreign 40: &nbsp;241-248',NULL,'',0),(419,'ANAGNOSTIDIS, K.',1961,'Untersuchungen über die Cyanophyceen einiger Thermen in Griechenland','Inst. Syst. Bot. &amp; Pflanzengeogr. Univ. Thessaloniki 7: &nbsp;1-322',NULL,'',0),(420,'SKUJA, H.',1939,'Beitrag zur Algenflora Lettlands II','<em>Acta Horti Botanici Universitatis Latviensis</em> 11/12: &nbsp;41-169',NULL,'',0),(421,'SHALYGIN, S., PIETRASIAK, N., GOMEZ, F., MLEWSKI, C., GERARD, E. & JOHANSEN, J.R.',2018,'Rivularia halophila sp. nov. (Nostocales, Cyanobacteria): the first species of Rivularia described with the modern polyphasic approach','European Journal of Phycology 53(4) 537-548',NULL,'https://doi.org/10.1080/09670262.2018.1479887',0),(422,'SKUJA, H.',1937,'Symbolae Sinicae. Botanische Ergebnisse der Expedition der Akademie der Wissenschaften in Wien nach Südwest-China 1914/1918','Verlag von J. Springer, Wien, (Eds. Handel-Mazzetti, H), &nbsp;Teil 1. Algae, , &nbsp;1-106 pp.',NULL,'',0),(423,'VORONICHIN, N.N.',1930,'Vodorosli Poljarnogo i Severnogo Urala','Trudy Leningradskogo Obsc. Estestvoisp., Vyp. 3, Ot. Bot. 60(3): 1-77',NULL,'',0),(424,'BOYE-PETERSEN, J.B.',1928,'On the knowledge of the fresh-water algae of Iceland','In: Rosenvinge, L.K. &amp; Warming, E. (Eds.) The botany of Iceland. Vol. II. Part II. Copenhagen &amp; London: Wheldon and Wesley, pp. 328-447',NULL,'',0),(425,'TILDEN, J.E.',1896,'American Algae','Century II, Minneapolis, Minnesota, No. 101-200',NULL,'',0),(426,'AGUILERA, A., BERRENDERO GOMEZ, E., KAŠTOVSKÝ, J., ECHENIQUE, R.O. & SALERNO, G.L.',2018,'The polyphasic analysis of two native Raphidiopsis isolates supports the unification of the genera Raphidiopsis and Cylindrospermopsis (Nostocales, Cyanobacteria)','Phycologia 57(2): 130-146',NULL,'https://dx.doi.org/10.2216/17-2.1',0),(427,'BOYE-PETERSEN, J.',1923,'The freshwater Cyanophyceae of Iceland','Arbejder fra den Botaniske have i København 101(7): &nbsp;251-324',NULL,'',0),(428,'FRÉMY, P.',1945,'Étude d\'une petite collection d\'Algues d\'eau douce de la Guinée Française','Bulletin du Muséum National d\'Histoire Naturelle, ser. 2, &nbsp;17(1): &nbsp;70-76',NULL,'',0),(429,'SENNA, P.A.C., SOUSA, M.G.M. & COMPERE, P.',1998,'A check-list of the algae of the Federal District (Brazil)','Scripta Botanica Belgica 16: &nbsp;12-88',NULL,'',0),(430,'WEST, W.',1892,'Algae of the English Lake District','Journal of the Royal Microscopical Society 1892, 6: 713-748',NULL,'',0),(431,'WANG, Y., CAI, F., JIA, N. & LI, R.',2019,'Description of a novel coccoid cyanobacterial genus and species Sinocapsa zengkensis gen. nov. sp. nov. (Sinocapsaceae, incertae sedis), with taxonomic notes on genera in Chroococcidiopsidales','Phytotaxa 409(3): 146-160',NULL,'https://doi.org/10.11646/phytotaxa.409.3.3',0),(432,'LEMMERMANN, E.',1911,'Algologische Beiträge VI','Archiv für Hydrobiologie und Planktonkunde 7: 364',NULL,'',1),(433,'TILDEN, J.E.',1898,'Observations on some west American thermal algae','Botanical Gazette 25: 89-105',NULL,'',0),(434,'DROUET, F.',1939,'The Myxophyceae of Maryland','Field Museum of Natural History, Botanical series 20(1): &nbsp;3-14',NULL,'',0),(435,'PRÁT, S.',1929,'<span data-field=\'publisher\' data-froala=\'light\' data-harvest=\'froala\' placeholder=\'Type something\'>Studie &nbsp;o biolithogenesi. Vápenité rasy a &nbsp;Cyanophyceae a jejich vyznam pri &nbsp;tvorení travertinu [Study on &nbsp;biolithogenesis. Calcareous race and &nbsp;Cyanophyceae and their role in &nbsp;creating travertine]</span>','&nbsp;Prague, Česká akademie věd a umění, pp. 1-187',NULL,'',0),(436,'FORTI, A.',1907,'Sylloge algarum omnium hucusque cognitarum. Vol. V. &nbsp;Sylloge Myxophycearum','Patavii, 761 pp.',NULL,'',0),(437,'GUARRERA, S.A. & KüHNEMANN, O.',1949,'Catálogo de las \'Chlorophyta\' y \'Cyanophyta\' de agua dulce de la República Argentina','Lilloa 19: &nbsp;219-318',NULL,'',0),(438,'RABENHORST, L.',1865,'Flora europaea algarum aquae dulcis et submarinae. Sectio II. Algas phycochromaceas complectens. &nbsp;pp. 1-319','Lipsiae, Apud Eduardum Kummerum, &nbsp;319 pp',NULL,'',0),(439,'KAMAT, N.D.',1963,'The algae of Kolhapur, India','Hydrobiologia 22: &nbsp;209-305',NULL,'',0),(440,'JAAG, O.',1935,'Eine neue Blaualge: <em>Plectonema capitata</em>','Bericht der schweizerischen botanischen Gessellschaft 44: &nbsp;437-442',NULL,'',0),(441,'ERCEGOVIC, A.',1932,'Ekoloske i socioloske studije o litofitskim cijanoficejama sa jugoslovenske obale Jadrana','Rad Jugoslovenske Akademije Znanosti i Umjetnosti, Zagreb 244: &nbsp;129-220',NULL,'',0),(442,'BISWAS, K.',1929,'Malayan aquatic biology. Freshwater algae with addendum','Journal Federated Malay States Museums 14:404–435',NULL,'',0),(443,'STARMACH, K.',1958,'<em>Lyngbya subclavata</em> n. sp. w Dolinie Roztoki w Tatrach','Fragmenta Floristica et Geobotanica Polonica 3(2): &nbsp;145-150',NULL,'',0),(444,'ZELLER, G.',1873,'Algae collected by Mr. S. Kurz in Arracan and British Burma, determined and systematically arranged by Dr. G. Zeller','The Journal of the Asiatic Society of Bengal 42(2): 1-269',NULL,'',0),(445,'SCHRAMM, A. & MAZÉ, H.',1865,'<em>Essai de classification des algues de la Guadeloupe</em>','&nbsp;Basse Terre, Guadeloupe: Imprimerie du Gouvernement, &nbsp;pp. [i]-ii, 1-52.',NULL,'',0),(446,'TSENG, C.K. & HUA, M.',1982,'On two new species of Gardnerula (Cyanophyta) and the taxonomy of the genera','Chinese Journal of Oceanography and Limnology 1(1): 111-120',NULL,'',0),(447,'WEBER VAN BOSSE, A.',1926,'Papers from Dr. Th. Mortensen\'s Pacific expedition 1914-16 XXXIII. Algues de l\'expédition danoise aux îles Kei','Videnskabelige Meddelelser Dansk Naturhistorisk Forening 81: &nbsp;57-155',NULL,'',0),(448,'BUCH, B., MARTINS, M.D. & BRANCO, L.H.Z.',2017,'A widespread &nbsp;cyanobacterium supported by polyphasic approach: proposition of <em>Koinonema pervagatum</em> gen. &amp; sp. &nbsp;nov. (Oscillatoriales)','.<em>Journal of Phycology</em> 53(5): &nbsp;1097-1105',NULL,'doi: 10.1111/jpy.12568',0),(449,'GONZÁLEZ-RESENDIZ, L., LEÓN-TEJERA, H.P., DÍAZ-LARREA, J., ALBA-LOIS, L., SEGAL-KISCHINEZKY, C.',2013,'Hassallia littoralis sp. nov. (Cyanobacteria, Microchaetaceae) from Mexico’s marine supralittoral based on morphological and molecular evidence','Phytotaxa 137(1): 35-47',NULL,'https://dx.doi.org/10.11646/phytotaxa.137.1.4',0),(450,'JAO, C.-C.',1944,'Studies on the fresh-water algae of China. XIII. New Myxophyceae from Kwangsi','Sinensia 15: &nbsp;75-90',NULL,'',0),(451,'ASENCIO, A.D., ABOAL, M. & HOFMANN, L.',1996,'A new cave-inhabiting blue-green alga: <em>Symphyonema cavernicolum</em> sp. nova (Mastigocladaceae, Stigonematales).','Arch. Hydrobiol./Algological Studies 83: 73-82',NULL,'',0),(452,'JOHANSEN J.R., BOHUNICKÁ, M., LUKEŠOVÁ, A., HRČKOVÁ, K., VACCARINO, M.A. & CHESARINO, N.M.',2013,'Morphological and molecular characterization within 26 strains of the genus Cylindrospermum (Nostocaceae, Cyanobacteria), with descriptions of three new species','Journal of Phycology 50: 187-202',NULL,'https://doi.org/10.1111/jpy.12150',0),(453,'BRüHL P. & BISWAS K.',1924,'&nbsp;Algae epiphyticae epiphloiae Indicae or Indian bark algae','J. Dept. Sci. Calcutta Univ. 5: 1-22&nbsp;',NULL,'',0),(454,'SOARES, F., TIAGO, I., TROVÃO, J., COELHO, C., MESQUITA, N., GIL, F., CATARINO, L., CARDOSO, S.M. & PORTUGAL. A.',2019,'Description of Myxacorys almedinensis sp. nov. (Synechococcales, Cyanobacteria) isolated from the limestone walls of the Old Cathedral of Coimbra, Portugal (UNESCO World Heritage Site)','Phytotaxa 419(1): 77-90',NULL,'https://doi.org/10.11646/phytotaxa.419.1.5',0),(455,'WILLE, N.',1914,'Süßwasseralgen von den Samoainseln, Hawaii, den Salomonsinseln und Ceylon, gesammelt von Dr. K. Rechinger','Denkschriften der Kaiserlichen Akademie der Wissenschaften [Wein], Mathematisch-naturwissenschaftliche Klasse 91: &nbsp;141-162',NULL,'',0),(456,'FRÉMY, A.',1923,'Description de deux Oscillariées nouvelles','Bulletin de la Société linnéenne de Normandie 7(6): 7-15',NULL,'',0),(457,'CHAKRABORTY, S., MARUTHANAYAGAM, V., ACHARI, A., PRAMANIK, A., PARASURAMAN, J. & MUKHERJEE, J.',2019,'Euryhalinema mangrovii gen. nov., sp. nov. and Leptoelongatus litoralis gen. nov., sp. nov. (Leptolyngbyaceae) isolated from an Indian mangrove forest','Phytotaxa 422(1): 58-74',NULL,'https://doi.org/10.11646/phytotaxa.422.1.4',0),(458,'FRÉMY, P.',1927,'&nbsp;Trois Oscilariées inédites trouvées dans l\'herbier Gomont','Bulletin du Museum National d\'Histoire Naturelle 33: 115-117',NULL,'',0),(459,'GHOSE, S.L.',1924,'A systematic and ecological account of a collection of blue-green algae from Lahore and Simla','Journal of the Linnean Society (Botany) 46: 333-346',NULL,'',0),(460,'HENTSCHE, G.S., RIGONATO, J., GENUÁRIO, D.B., LAUGHINGHOUSE IV., H.D. & SANT´ANNA, C.L.',2019,'Morphological and molecular characterization of Stigonema jureiensis sp. nov. (Nostocales, Cyanobacteria) from the Atlantic Rainforest, São Paulo, Brazil','Fottea 19(2): 185-191',NULL,'https://doi.org/10.5507/fot.2019.009',0),(461,'RADZI, R., MUANGMAI, N., BROADY, P., OMAR, W.M.W., LAVOUE, S., CONVEY, P. & MERICAN, F.',2019,'Nodosilinea signiensis sp. nov. (Leptolyngbyaceae, Synechococcales), a new terrestrial cyanobacterium isolated from mats collected on Signy Island, South Orkney Islands, Antarctica','PLoS ONE 14(11): e0224395',NULL,'https://doi.org/ 10.1371/journal.pone.0224395',0),(462,'KAŠTOVSKÝ, J., VESELÁ, J., BOHUNICKÁ, M.,  FUČÍKOVÁ, K., ŠTENCLOVÁ, L. & BREWER-CARIAS, C.',2016,'New and unusual species of cyanobacteria, diatoms and green algae, with a description of a new genus <em>Ekerewekia</em> gen. nov. (Chlorophyta) from the table mountain Churí-tepui, Chimantá Massif (Venezuela).&nbsp;','Phytotaxa 247(3): &nbsp;153-180',NULL,'http://dx.doi.org/10.11646/phytotaxa.247.3.1',0),(463,'DROUET, F.',1937,'The Brazilian Myxophyceae. I.','<em>American Journal of Botany</em> 24(9): &nbsp;598-608',NULL,'',0),(464,'ANAGNOSTIDIS, K.',1989,'<em>Geitlerinema</em>, a new genus of oscillatorialean cyanophytes.','Plant Systematics and Evolution 164: 33-46',NULL,'',0),(465,'DROUET, F.',1942,'Studies in Myxophyceae. I.&nbsp;','Publications of the Field Museum of Natural History, Botanical Series 20(6): &nbsp;123-141',NULL,'',0),(466,'KüTZING, F.T.',1849,'Species algarum.','&nbsp;F.A. Brockhaus. Leipzig, 922 pp',NULL,'',0),(467,'GONZÁLEZ GUERRERO, P.',1946,'Cianofíceas y algas continentales de Cádiz','Anales Jardín Botánico de Madrid 6(1): 237-335.',NULL,'',0),(468,'SETCHELL, W.A. & GARDNER, N.L.',1924,'XXIX Expedition of the California Academy of Sciences to the Gulf of California in 1921. The marine algae.','Proceedings of the California Academy of Science, Fourth Series 12(29): 695-949',NULL,'',0),(469,'GARDNER, N.L.',1927,'On a collection of Myxophyceae from Fukien Province, China','<em>University of California Publications in Botany</em> 14(1): &nbsp;1-20',NULL,'',0),(470,'UMEZAKI, I.',1995,'Marine blue-green algae from Palawan in the Philippines. 1. Chroococcales and Oscillatoriales.','Journal of Japanese Botany 70(3): &nbsp;123-139',NULL,'',0),(471,'SARAF, A., GAWDA, H.G., SUDKAR, A., BATULE, P., BEHERE, I., KOTULKAR, M., KUMAT, A. & SINGH, P.',2018,'Insights into the phylogeny of false-branching heterocytous cyanobacteria with the description of Scytonema pachmarhiense sp. nov. isolated from Pachmarhi Biosphere Reserve, India','FEMS Microbiology Letters 365: fny160',NULL,'https://dx.doi.org/10.1093/femsle/fny160',0),(472,'CAIRES, T.A.',2019,'<em>Capilliphycus </em>gen. nov.; validation of “Capillus T.A.Caires, Sant’Anna &amp; J.M.Nunes,” inval. (Oscillatoriaceae, Cyanobacteria)','Notulae Algarum No. 95',NULL,'http://www.notulaealgarum.com/documents/Notulae%20algarum%20No.%2095.pdf',0),(473,'DROUET, F.',1943,'Myxophyceae of eastern California &nbsp;and western Nevada.&nbsp;','Botanical Series Field Museum of Natural History 20: &nbsp;145-176',NULL,'',0),(474,'HAUCK, F. & RICHTER, P.',1892,'Phykotheka universalis','&nbsp;Fasc. I-XV (1885-1896) - exsiccata &nbsp;no. 1-750. Leipzig',NULL,'',0),(475,'MARTENS, G.',1869,'Beiträge zur Algen-Flora Indiens','Flora oder Allgemaine Botanische Zeitung 52: 233-238',NULL,'',0),(476,'SARAF, A., SURADKAR, A., DAWDA, H.G., GAYSINA, L.A., GABIDULLIN, Y., KUMAT, A., BEHERE, I., KOTULKAR, M., BATULE, P. & SINGH, P.',2019,'Phylogenetic complexities of the members of Rivulariaceae with the re-creation of the family Calotrichaceae and description of Dulcicalothrix necridiiformans gen nov., sp nov., and reclassification of Calothrix desertica','FEMS Microbiology Letters 366: fnz219',NULL,'https://doi.org/10.1093/femsle/fnz219',0),(477,'MARTENS, G.',1871,'A fifth list of Bengal Algae determined by Dr. G. Martens communicated by Mr. S. Kurz','Proceedings of the Asiatic Society Bengal 1871: 170-173',NULL,'',0),(478,'TAWONG, W., PONGCHAROEN, P., PONGPADUNG, P. & PONZA, S.',2019,'Neowollea manoromense gen. &amp; sp. nov. (Nostocales, Cyanobacteria), a novel geosmin producer isolated from Thailand','Phytotaxa 424(1): 1-17',NULL,'https://doi.org/10.11646/phytotaxa.424.1.1',0),(479,'HOLDEN, I.',1899,'Two new species of marine algae from Bridgeport, Connecticut','Rhodora 1: 197-198',NULL,'',0),(480,'WITTROCK, V.B. & NORDSTEDT, C.F.O.',1889,'Literatur-öfversigt [Literature review]. Algae aquae dulcis exsiccatae praecipue Scandinavicae quas adjectis algis marinis chlorophyllaceis et phycochromaceis.','Botaniska Notiser 1889(4): 157-171',NULL,'',0),(481,'HANSGIRG, A.',1892,'Beiträge zur Kenntniss der Süsswasser-Algen und Bacterien-Flora von Tirol und Böhmen.','Sitzungsberichte der Königl. Böhmischen Gesellschaft der Wissenschaften. Mathematisch-naturwissenschaftliche Classe 1892: 105-156',NULL,'',0),(482,'NOVICHKOVA, L.N.',1960,'Novye i interesnye sinezelenye vodorsli Takrov. (Algae Cyanophyceae novae et curiosae e Takyris.)','Botaniceskie Materialy Instituta Sporovyh Rastenij Glavnogo &nbsp;Botaniceskogo Sada RSFSR. (Notulae Systematicae ex Instituto Cryptogamico &nbsp;Horti Botanici Petropolitani Reipublicae Rossicae) 13: &nbsp;30-34.',NULL,'',0),(483,'LUCAS, A.H.S.',1919,'Notes on Australian marine algae, II','&nbsp;Proceedings of the Linnean Society of New South Wales 44: 174-179',NULL,'',0),(484,'GOMONT, M.',1890,'Essai de classification des Nostocacées homocystées.','Journal de Botanique [Morot] 4: 349-357',NULL,'',0),(485,'DROUET F.',1960,'Albanian algae collected by Guiseppe De Toni','Revue Algologique, Nouvelle Série 5(2): &nbsp;111-115',NULL,'',0),(486,'PIETRASIAK, N., MüHLSTEINOVÁ, R., SIEGESMUND, M.A. & JOHANSEN, J.R.',2014,'Phylogenetic placement of <em>Symplocastrum</em> (Phormidiaceae, Cyanophyceae) with a new combination <em>S. californicum</em> and two new species: <em>S. flechtnerae</em> and <em>S. torsivum</em>','Phycologia 53(6): &nbsp;529-541',NULL,'DOI: 10.2216/14-029.1',0),(487,'DROUET, F.',1943,'New species of Oscillatoriaceae','American Midland Naturalist 29(1): &nbsp;51-54.',NULL,'',0),(488,'FRIEDMANN, I.',1955,'Geilteria calcarea n. gen. et n. sp. A new atmophytic lime-incrusting blue-ggreen alga.','Bot. Notiser 108(4): 439-445',NULL,'',0),(489,'CASAMATTA, D.A., VILLANUEVA, C.D., GARVEY, A.D., STOCKS, H.S., VACCARINO, M., DVOŘÁK, P., HAŠLER, P. & JOHANSEN, J.R.',2020,'Reptodigitus chapmanii (Nostocales, Hapalosiphonaceae) gen. nov.: A unique nostocalean (Cyanobacteria) genus based on polyphasic approach','Journal of Phycology 56: 425-436',NULL,'https://dx.doi.org/10.1111/jpy.12954',0),(490,'BRANCO, L.H.Z., AZEVEDO, M.T.P., SANT\'ANNA, C.L. & KOMÁREK, J.',2006,'New morphospecies of <em>Symplocastrum</em> (Phormidiaceae, Oscillatoriales) from aerophytic habitats in Brazil.&nbsp;','Algological Studies 121: &nbsp;23-33',NULL,'',0),(491,'KIRCHNER, O.',1900,'Schizophyceae','In: &nbsp;ENGLER, A. &amp; PRANTL K. (eds.) Die natürlichen Pflanzenfamilien...I. Teil, Abt. 1a. &nbsp;pp. 45-92. Leipzig',NULL,'',0),(492,'KüTZING, F.T.',1847,'Diagnosen und Bemerkungen zu neuen oder kritischen Algen.','Botanische Zeitung 5: 193-198',NULL,'',0),(493,'WEST, W. & WEST, G.S.',1896,'On some new and interesting freshwater algae','Journal of the Royal Microscopical Society 16: &nbsp;149-165',NULL,'',0),(494,'WEST, W. & WEST, G.S.',1894,'&nbsp;On some freshwater algae from the West Indies','Journal of the Linnean Society of London, Botany 30: 264-280',NULL,'',0),(495,'RINO, J.A.',1972,'Contribuçao para o conhecimento das algas de agua doce de Moçambique III.&nbsp;','Revista de Ciências Biológicas, Série A 5: &nbsp;121-264',NULL,'',0),(496,'LEMMERMANN, E.',1908,'Algologische Beiträge VI.&nbsp;','<em>Archiv für Hydrobiologie und Planktonkunde: neue Folge der Forschungsberichte aus der Biologischen Station zu Plön</em> 4: &nbsp;165-192.',NULL,'',0),(497,'CAI, F., WANG, Y., YU, G., WANG, J., PENG, X. & Li, R.',2020,'Proposal of Purpurea gen. nov. (Nostocales, Cyanobacteria), a novel cyanobacterial genus from wet soil samples in Tibet, China','Fottea 2020(1): 86-97',NULL,'https://dx.doi.org/10.5507/fot.2019.018',0),(498,'.SCHMIDLE, W.',1903,'Berichte über die botanischen Ergebnisse der Nyassa-See und Kinga-Gerbirgs-Expedition der Hermann-und Elise-geb. Heckmann-Wentzel-Stiftung. V. Algen, insbesondere Solche des Plankton, aus dem Nyassa-See und seinen Umgebung, gesammelt von Dr. Fülleborn','Botanische Jahrbücher für Systematik Pflanzengeschichte und Pflanzengeographie 32: 56-88',NULL,'',0),(499,'SCHMIDLE, W.',1903,'Berichte über die botanischen Ergebnisse der Nyassa-See und &nbsp;Kinga-Gerbirgs-Expedition der Hermann-und Elise-geb. &nbsp;Heckmann-Wentzel-Stiftung. V. Algen, insbesondere Solche des Plankton, &nbsp;aus dem Nyassa-See und seinen Umgebung, gesammelt von Dr. Fülleborn.','Botanische Jahrbücher für Systematik Pflanzengeschichte und Pflanzengeographie 32: &nbsp;56-88.',NULL,'',0),(500,'SETCHELL, W.A.',1895,'Notes on some Cyanophyceae of New England','Bulletin of the Torrey Botanical Club 22: &nbsp;424-431',NULL,'',0),(501,'VASISHTA, P.C.',1963,'Five new cyanophyceae from Hoshiarpur.','<em>J</em>ournal of the Indian Botanical Society 42(4): 574 582',NULL,'',0),(502,'SETCHELL, W.A.',1924,'&nbsp;American Samoa: Part I. Vegetation of Tutuila &nbsp;Island Part II. Ethnobotany of the Samoans Part III. Vegetation of Rose &nbsp;Atoll.&nbsp;','Publications of the Carnegie Institution of Washington 341: 1-275',NULL,'',0),(503,'RACIBORSKI, M.',1910,'Phycotheca Polonica','Kosmos 35: 80-89',NULL,'',0),(504,'WITTROCK, V.B. & NORDSTEDT, C.F.O.',1884,'Algae aquae dulcis exsiccatae praecipue Scandinavicae quas adjectis chlorophyllaceis et phycochromaceis distribuerunt','Botaniska Notiser 1884: 121-128',NULL,'',0),(505,'MARGIN, A.G.E., SENNA, P.A.C. & KOMÁREK, J.',1997,'<em>Arthrospira skujae</em>, a new planktic tropical cyanoprokaryote.&nbsp;','Archiv für Protistenkunde 148(4):479-489',NULL,'',0),(506,'BRüHL, P. & BISWAS, K.',1922,'Commentationes algologicae. I. The algae of Bengal filter-beds','Journal of the Department of Science, University of Calcutta 4(Botany:1): 1-17',NULL,'',0),(507,'SENNA, P.A.C. & KOMÁREK, J.',1998,'<em>Dasygloea brasiliensis</em>, (syn.: <em>Lyngbya brasiliensis</em>) cyanoprokaryotes from the central part (\'cerrados\') of Brazil.&nbsp;','Algological Studies 88: 1-16',NULL,'',0),(508,'SCHAARCHMIDT, J.',1886,'Notes on Afghanistan algae.&nbsp;','<em>Journal of the Linnean Society of London Botany</em> 21(134): 241-250',NULL,'',0),(509,'DESIKACHARY,T.V.',1959,'<em><i>Cyanophyta</i></em>. 686 pp&nbsp;','New Delhi: Indian Council of Agricultural Research.',NULL,'',0),(510,'FRÉMY, P.',1932,'Cyanophycées vivant dans le thalle des <em>Codium</em>.&nbsp;','Compte Rendu Hebdomadaire des Séances de l\'Académie des Sciences. Paris 195: 1413-1414',NULL,'',0),(511,'VORONICHIN, N.N.',1932,'K poznanyu flory i rastitelnosti vodoroslej presnych vodoemov Kryma.&nbsp;','Botaničeskij Žurnal 17: 265-325',NULL,'',0),(512,'HARVEY, W.H.',1841,'<em>A manual of the British algae</em>: containing generic and specific descriptions of the known British species of sea-weeds and of <em>Confervae</em> both marine and fresh-water.&nbsp;','pp. 229. London: John Van Voorst',NULL,'',0),(513,'MEYER, K.J.',1924,'Fitoplankton reki Oki u g. Muroma v 1922 godu','Raboty okskoj biologiceskoj stancii 3, 1: 53-57',NULL,'',0),(514,'STARMACH, K.',1960,'<em>Microcoleus erectiusculus</em> sp. n.&nbsp;','Fragmenta Floristica et Geobotanica Polonica 6(4): &nbsp;769-772',NULL,'',0),(515,'HASSALL, A.H.',1845,'<em>A history of the British freshwater algae</em>, including descriptions of the Desmideae and Diatomaceae. With upwards of one hundred plates, illustrating the various species.&nbsp;','London, Edinburgh, Paris &amp; Leipzig: S. Highley, H. Baillière; Sunderland &amp; Knox; J.B. Baillière; T.O. Weigel, 462 pp.',NULL,'',0),(516,'MAZÉ, H.',1868,'Hydrophytes de la Guyane Française: nomenclature générale des plantes cellulaires de la Guyane recueillies par divers de 1835 a 1868.','Basse-Terre (Guadeloupe), 41 pp.',NULL,'',0),(517,'JAAG, O.',1938,'Die Kryptogamenflora des Rhein-falls und des Hochrheins von Stein bis Eglisau.','Mitteilungen der Naturforschenden Gesellschaft Schaffhausen, Zürich 14: 1-158',NULL,'',0),(518,'SETCHELL, W.A.& GARDNER, N.L.',1937,'The Templeton crocker expedition of the California Academy of Sciences 1932, No31- A Preliminary report on the algae&nbsp;','Proceedings of the California Academy of Science, series 4, 22: 65-98',NULL,'',0),(519,'KIRCHNER, O.',1878,'&nbsp;Algen','Kryptogamen-Flora von Schlesien. Part 1. Breslau: Kern\'s Verlag, 284 pp.',NULL,'',0),(520,'SCHMIDLE,  W.',1897,'Algologische Notizen. IV.&nbsp;','Allgemeine botanische Zeitschrift für Systematik, Floristik, Pflanzengeographie 4: 57-58.',NULL,'',0),(521,'RABENHORST, G.L.',1847,'<em>Deutschlands Kryptogamen-Flora</em> oder Handbuch zur Bestimmung der kryptogamischen Gewächse Deutschlands, der Schweiz, des Lombardisch-Venetianischen Königreichs und Istriens. Zweiter Band. Zweite Abteilung: Algen','Leipzig: Verlag von Eduard Kummer. 216 pp.',NULL,'',0),(522,'TSENG, C.K.',1983,'Common Seaweeds of China','Beijing: Science Press, 318 pp.',NULL,'',0),(523,'NODA, M.',1963,'Freshwater algae of north-eastern China','Journal of Faculty of Science Niagata University, series 2 4(3): 105-178',NULL,'',0),(524,'BORY de Saint-Vincent, J.B.',1826,'Dictionnaire Classique D´Histoire Naturelle 10: 1-642','Rey et Gravier Libraires-Éditeurs, &nbsp;Paris&nbsp;',NULL,'',0),(525,'HANSGIRG, A.',1890,'Über neue Süsswasser- und Meeres-Algen und Bacterien, mit Bemerkungen zur Systematik dieser Phycophyten und über den Einfluss des Lichtes auf die Ortsbewegungen des <em>Bacillus pfefferi</em> nob.&nbsp;','Sitzungsberichte der Königlichen Böhmischen Gesellschaft der Wissenschaften, Mathematisch-naturwissenschaftliche Classe 1890(1): 3-34',NULL,'',0),(526,'DROUET, F.',1939,'Francis Wolle\'s filamentous Myxophyceae','Field Museum of Natural History. Botanical series 20(2): 17-64.',NULL,'',0),(527,'TILDEN, J.E.',1896,'American Algae','Century II, No. 175',NULL,'',1),(528,'CASTAGNE, L.',1851,'Supplément &nbsp;au cataloque de plants qui croissent naturellement &nbsp;aux &nbsp;environs de Marseille.&nbsp;','Aix 125 pp.',NULL,'',0),(529,'SANTRA, S.C.',1984,'&nbsp;Algal flora of Sikkim Himalaya - I: A contribution to our knowledge of the blue-green algae of North-East Sikkim (India)','<em>Journal of Economic and Taxonomic Botany</em> 5(5): 1209-1219',NULL,'',0),(530,'JAO, C.C.',1939,'Studies on the freshwater algae of China. IV. Subaerial and aquatic algae from Nanyoh, Hunan','<em>Sinensia</em> 10: 161-239',NULL,'',0),(531,'VOUK,V.',1916,'Bioloska istrazivanja terminali voda Hrvatskoga Zagorja','<em>Jugoslav. Akad. Prir. Istraz. Hrvatske i Slavonije</em> 8(1): 1-17',NULL,'',0),(532,'BROADY, P.A. & INGERFELD, M.',1991,'<em>Placoma regulare </em>sp. nov. (<em>Entophysalidaceae</em>, Cyanobacteria) from New Zealand streams','Phycologia 30(6): 547-555',NULL,'',0),(533,'LV, H.-R., WANG, J., LV, J.-P., LIU, Q. & XIE, S.-L.',2017,'Synechococcus salsus sp. nov. (Cyanobacteria): A new unicellular, coccoid species from Yuncheng Salt Lake, North China','Bangladesh Journal of Plant Taxonomy 24(2): 137-147',NULL,'https://www.banglajol.info/index.php/BJPT/article/view/35109/23694',0),(534,'CAI, F., PENG, X. & LI, R.',2020,'Violetonostoc minutum gen. et sp. nov. (Nostocales, Cyanobacteria) from a rocky substrate in China','Algae 35(1): 1-15',NULL,'https://doi.org/10.4490/algae.2020.35.3.4',0),(535,'BORNET, E.',1892,'Les algues de P.-K.-A. Schousboe','Mémoires de la Société des Sciences Naturelles et Mathématiques de Cherbourg 28: &nbsp;165-376',NULL,'',0),(536,'MAREŠ, J., HAUER, T., KOMÁREK, J. & COMPERE, P.',2013,'(2195) Proposal to conserve the name Gloeothece (Cyanophyceae) with a conserved type','Taxon 62(5): 1056',NULL,'https://dx.doi.org/10.12705/625.24',0),(537,'PRINGSHEIM, E.G.',1965,'<em>Oscillatoria agardhii</em> var. <em>suspensa</em> nov. var','Archives of Microbiology 50(4): 401-413',NULL,'',0),(538,'GENUÁRIO, D.B., SOUZA, W.R., SANT´ANNA, C.L., MONTEIRO, R.T.R.& MELO, I.S.',2020,'Erratum: Amazoninema gen. nov., (Synechococcales, Pseudanabaenaceae) a novel cyanobacteria genus from Brazilian Amazonian rivers','International Journal of Systematic and Evolutionary Microbiology 70: 1441-1442',NULL,'https://dx.doi.org/10.1099/ijsem.0.003849',1),(539,'SHALYGIN, S., SHALYGINA, R.R., REDKINA, V.V., GARGAS, C.B. & JOHANSEN, J.R.',2020,'Description of Stenomitos kolaenensis and S. hiloensis sp. nov. (Leptolyngbyaceae, Cyanobacteria) with an emendation of the genus','Phytotaxa 440(2): 108-128',NULL,'https://doi.org/10.11646/phytotaxa.440.2.3',0),(540,'MORO, I., RASCIO, N., LA ROCCA, N., DI BELLA, M. & ANDREOLI, C.',2007,'Cyanobacterium aponinum, a new Cyanprokaryote from the microbial mat of Euganean thermal springs (Padua, Italy)','Algological studies 123: 1-15',NULL,'',0),(541,'DAVYDOV, D., SHALYGIN, S. & VILNET, A.',2020,'New cyanobacterium Nodosilinea svalbardensis sp. nov. (Prochlorotrichaceae, Synechococcales) isolated from alluvium in Mimer river valley of the Svalbard archipelago','Phytotaxa 442 (2): 061–079',NULL,'https://doi.org/10.11646/phytotaxa.442.2.2',0),(542,'LI, Z., MERTENS, K.N., CHOI, H.J. & SHIN, H.H.',2020,'Validation of “Dolichospermum hangangense H.J.Choi &amp; M.-S.Han,” nom. inval.(Aphanizomenonaceae, Cyanobacteria) from Han River, Korea','Notulae Algarum 124',NULL,'http://www.notulaealgarum.com/2020/documents/Notulae%20algarum%20No.%20124.pdf',0),(543,'RADZI, R. & MERICAN, F.',2020,'Validation of &nbsp;“Nodosilinea signiensis R.Radzi &amp; F.Merican,” nom. inval. (Prochlorotrich-aceae, Cyanophyceae)&nbsp;','Notulae Algarum 125',NULL,'http://www.notulaealgarum.com/2020/documents/Notulae%20algarum%20No.%20125.pdf',0),(544,'CAI, F. & Li, R.',2019,'Validation of Compactonostoc shennongjiaensegen. et sp. nov. (Nostocaceae, Cyanobacteria)','Notulae Algarum 121',NULL,'http://www.notulaealgarum.com/documents/Notulae%20Algarum%20No.%20121.pdf',0),(545,'TRONHOLM, A. & ENGENE, N.',2019,'Moorena gen. nov., a valid name for “Moorea Engene &amp; al.” nom. inval. (Oscillatoriaceae, Cyanobacteria)&nbsp;','Notulae Algarum 122',NULL,'http://www.notulaealgarum.com/documents/Notulae%20algarum%20No.%20122.pdf',0),(546,'GENUÁRIO, D.B., SOUZA, W.R., SANT´ANNA, C.L., MONTEIRO, R.T.R. & MELO, I.S.',2020,'Erratum: Amazoninema gen. nov., (Synechococcales, Pseudanabaenaceae) a novel cyanobacteria genus from Brazilian Amazonian rivers','International Journal of Systematic and Evolutionary Microbiology 70: 1441-1442',NULL,'https://dx.doi.org/10.1099/ijsem.0.003849',0),(547,'OSORIO-SANTOS, K., PIETRASIAK, N., BOHUNICKÁ, M., MISCOE, L.H., KOVÁČIL, L., MARTIN, M.P. & JOHANSEN, J.R.',2014,'Seven new species of Oculatella (Pseudanabaenales, Cyanobacteria): taxonomically recognizing cryptic diversification','European Journal of Phycology 49(4): 450-470',NULL,'https://doi.org/10.1080/09670262.2014.976843',0),(548,'LEE, N.-J., SEO, Y., KI, J.-S. & LEE, O.-M.',2020,'Morphology and molecular description of Wilmottia koreana sp. nov. Oscillatoriales, Cyanobacteria) isolated from the Republic of Korea','Phytotaxa 447(4): 237-251',NULL,'https://doi.org/10.11646/phytotaxa.447.4.2',0),(549,'SINGH, P., ŠNOKHOUSOVÁ, J., SARAF, A., SURADKAR, A. & ELSTER, J.',2020,'Phylogenetic evaluation of the genus Nostoc and description of Nostoc neudorfense sp. nov., from the Czech Republic','International Journal of Systematic and Evolutionary Bacteriology 70: 2740–2749',NULL,'https://doi.org/10.1099/ijsem.0.004102',0),(550,'SARAF, A., DAWDA, H.G., SUDKAR, A., AGRE, V. & SINGH, P.',2020,'Fortiea necridiiformans sp. nov., a soil-dwelling cyanobacterium from Pachmarhi Biosphere Reserve, India','International Journal of Systematic and Evolutionary Microbiology',NULL,'https://dx.doi.org/10.1099/ijsem.0.004337',0),(551,'JUNG, P., MIKHAILYUK, T., EMRICH, D., BAUMANN, K., DULTZ, S. & BÜDEL, B.',2020,'Shifting Boundaries: Ecological and Geographical Range extension Based on Three New Species in the Cyanobacterial Genera Cyanocohniella, Oculatella, and, Aliterella','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13025',0),(552,'MISHRA, D., SURADKAR, A., SARAF, A. & SINGH, P.',2020,'Phylogenetic evaluation of the true-branched heterocytous cyanobacteria and description of soil dwelling Westiellopsis akinetica sp. nov.','FEMS MIcrobiology Letters 367(5): fnaa046',NULL,'https://doi.org/10.1093/femsle/fnaa046',0),(553,'KOMÁREK, J., KOMÁRKOVÁ, J., VENTURA, S., KOZLÍKOVÁ-ZAPOMĚLOVÁ, E. & REJMÁNKOVÁ, E.',2017,'Taxonomic evaluation of cyanobacterial microflora from alkaline marshes of northern Belize. 3. Diversity of heterocytous genera','Nova Hedwigia 105(3-4): 445-486',NULL,'https://doi.org/10.1127/nova_hedwigia/2017/0425',0),(554,'BERTHOLD, D.E., LEFLER, F.W., WERNER, V.R. & LAUGHINGHOUSE IV, D.H.',2020,'Johannesbaptistia floridana sp. nov. (Chroococcales, Cyanobacteria), a novel marine cyanobacterium from coastal South Florida (USA)','Fottea 20(2): 152-159',NULL,'https://doi.org/10.5507/fot.2020.008',0),(555,'CAI, F.F. & LI, R.H.',2020,'Purpureonostoc, a new name for a recently described genus of Nostoc–like cyanobacteria','Fottea 20(2):111',NULL,'https://doi.org/10.5507/fot.2020.007',0),(556,'BECERRA-ABSALÓN, I., JOHANSEN, J.R., OSORIO-SANTOS, K. & MONTEJANO, G.',2020,'Two new Oculatella (Oculatellaceae, Cyanobacteria) species in soil crusts from tropical semi–arid uplands of México','Fottea 20(2): 160-170',NULL,'https://doi.org/10.5507/fot.2020.010',0),(557,'TUJI, A. & NIIYAMA, Y.',2018,'Two new Pseudanabaena (Cyanobacteria, Synechococcales) species from Japan, Pseudanabaena cinerea and Pseudanabaena yagii, which produce 2-methylisoborneol','Phycological Research 66: 291-299',NULL,'https://doi.org/10.1111/pre.12327',0),(558,'ZIMBA, P.V., SHALYGIN, S., HUANG, I.-S., MOMČILOVIĆ, M. & ABDULA, H.',2020,'A new boring toxin producer – Perforafilum tunnelli gen. &amp; sp. nov. (Oscillatoriales, Cyanobacteria) isolated from Laguna Madre, Texas, USA','Phycologia',NULL,'https://doi.org/10.1080/00318884.2020.1808389',0),(559,'SOARES, F., RAMOS, V., TROVAO, J., CARDOSO, S.M., TIAGO, I. & PORTUGAL, A.',2020,'Parakomarekiella sesnandensis gen. et sp. nov. (Nostocales, Cyanobacteria) isolated from the Old Cathedral of Coimbra, Portugal (UNESCO World Heritage Site)','European Journal of Phycology',NULL,'https://doi.org/10.1080/09670262.2020.1817568',0),(560,'KONSTANTINOU, D., VOULTSIADOU, E., PANTERIS, E. & GKELIS, S.',2021,'Revealing new sponge-associated cyanobacterial diversity: Novel genera and species','Molecular Phylogenetics and Evolution 155: 106991',NULL,'https://doi.org/10.1016/j.ympev.2020.106991',0),(561,'DUVAL, C., HAMLAOUI, S., PIQUET, B., TOUTIRAIS, G., YÉPRÉMIAN, C., REINHARDT, A., DUPERRON, S., MARIE, B., DEMAY, J. & BERNARD, C.',2021,'Diversity of cyanobacteria from thermal muds (Balaruc-Les-Bains, France) with the description of <em>Pseudochroococcus coutei</em> gen. nov., sp. nov.','FEMS Microbes 2: xtab006',NULL,'https://doi.org/10.1093/femsmc/xtab006',0),(562,'PIETRASIAK, N., REEVE, S, OSORIO-SANTOS, K., LIPSON D.A. & JOHANSEN J.R.',2021,'Trichotorquatus gen. nov. - A new genus of soil cyanobacteria discovered from American drylands','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13147',0),(563,'GENG, R., WANG, Y., CAI, F., ZHANG, Y., YANG, P., DAI, G., LI, R. & YU, G.',2021,'Neochroococcus gongqingensis gen. et sp. nov., a new member of coccoid cyanobacteria from a watercourse, Eastern China','Fottea 21(1): 44-52',NULL,'https://doi.org/10.5507/fot.2020.015',0),(564,'BARBOSA, M., BERTHOLD, D.E., LEFLER, F.W. & LAUGHINGHOUSE, D. H.',2021,'Diversity of the genus Brasilonema (Nostocales, Cyanobacteria) in plant nurseries of central Florida (USA) with the description of three new species: B. fioreae sp. nov., B. santannae sp. nov. and B. wernerae sp. nov.','Fottea 21(1): 82-99',NULL,'https://doi.og/10.5507/fot.2020.019',0),(565,'TUJI, A., YAMAGUCHI, H., KATAOKA, T., SATO, M., SANO, T. & NIIYAMA, Y.',2021,'Annamia dubia sp. nov. with a description of a new family, Geminocystaceae fam. nov. (Cyanobacteria)','Fottea 21(1): 100-109',NULL,'https://doi.org/10.5507/fot.2021.003',0),(566,'JAISWAL, T.P., CHAKRABORTY, S., SINGH, P., MISHRA, A.K. & SINGH, S.S.',2021,'Description of hot spring dwelling <em>Mastigocladus ambikapurensis</em> sp. nov., using a polyphasic approach','Plant Systematics and Evolution 307:33',NULL,'https://doi.org/10.1007/s00606-021-01755-2',0),(567,'JUNG, P., D´AGOSTINO, P.M., BÜDEL, B. & LAKATOS, M.',2021,'<em>Symphyonema bifilamentata</em> sp. nov., the Right <em>Fischerella ambigua</em> 108b: Half a Decade of Research on Taxonomy and Bioactive Compounds in New Light','Microorganisms 9:745',NULL,'https://doi.org/10.3390/microorganisms9040745',0),(568,'BERTHOLD, D.E., LEFLER, F.W., HUANG, I-S., ABDULLA, H., ZIMBA, P.V. & LAUGHINGHOUSE IV, H.D.',2021,'Iningainema tapete sp. nov. (Scytonemataceae, Cyanobacteria) from greenhouses in central Florida (USA) produces two types of nodularin with biosynthetic potential for microcystin-LR and anabaenopeptin production','Harmful Algae 101: 102969',NULL,'https://doi.org/10.1016/j.hal.2020.101969',0),(569,'BERTHOLD, D.E., LEFLER, F.W. & LAUGHINGHOUSE IV, H.D.',2021,'Untangling filamentous marine cyanobacterial diversity from the coast of South Florida with the description of Vermifilaceae fam. nov. and three new genera:<em> Leptochromothrix</em> gen. nov., <em>Ophiophycus </em>gen. nov., and <em>Vermifilum </em>gen. nov.','Molecular Phylogenetics and Evolution',NULL,'https://doi.org/10.1016/j.ympev.2020.107010',0),(570,'MALTSEV, Y., KEZLYA, E., MALTSEVA, S., KARTHICK, B., DVOŘÁK, P., KOCIOLEK, J.P. & KULIKOVSIY, M.',2021,'A new species of the previously monotypic genus Iningainema (Cyanobacteria, Scytonemataceae) from the Western Ghats, India','European Journal of Phycology',NULL,'https://doi.org/10.1080/09670262.2020.1834147',0),(571,'LEFLER, F.W., BERTHOLD, D.E. & LAIGHINGHOUSE IV, H.D.',2021,'The occurrence of Affixifilum gen. nov. and Neolyngbya (Oscillatoriaceae) in South Florida (USA), with the description od A. floridanum sp. nov and N. biscayensis sp. nov.','Journal of Phycology 57: 92-110',NULL,'https://doi.org/10.1111/jpy.13065-20-095',0),(572,'CURREN, E. & LEONG, S.CH.Y.',2018,'<em>Lyngbya regalis</em> sp. nov. (Oscillatoriales, Cyanophyceae), a new tropical marine cyanobacterium','Phytotaxa 367(2): 120-132',NULL,'https://doi.org/10.11646/phytotaxa.367.2.2',0),(573,'LAUGHINGHOUSE IV, H.D., LEFLER, F.W. & BERTHOLD, D.E.',2021,'Validation of the designation “Neolyngbya regalis”, nom. inval. (Oscillatoriaceae, Cyanobacteria)','Notulae algarum No. 182',NULL,'https://notulaealgarum.org/2021/documents/Notulae%20Algarum%20No.%20182.pdf',0),(574,'KOMÁREK, J., JOHANSEN, J.R., ŠMARDA, J. & STRUNECKÝ, O.',2020,'Phylogeny and taxonomy of Synechococcus–like cyanobacteria','Fottea 20(2): 171-191',NULL,'https://doi.org/10.5507/fot.2020.006',0),(575,'Dor, I.',1967,'Algues des sources thermales de Tiberiade','Lake Tiberias investigations 5: 3-29',NULL,'',0),(576,'NOWRUZI, B. & SOARES, F.',2021,'Alborzia kermanshahica gen. nov., sp. nov. (Chroococcales, Cyanobacteria), isolated from paddy fields in Iran','International Journal of Systematic and Evolutionary Microbiology',NULL,'https://doi.org/10.1099/ijsem.0.004828',0),(577,'RIGONATO, J., SANT´ANNA, C.L., GIANI, A., AZEVEDO, M.T.P., GAMA, W.A., VIANA, V.F.L., FIORE, M.F. & WERNER, V.R.R',2018,'Sphaerocavum: a coccoid morphogenus identical to Microcystis in terms of 16S rDNA and ITS sequence phylogenies','Hydrobiologia 81:35-48',NULL,'https://doi.org/10.1007/s10750-017-3312-2',0),(578,'SARAF, A., DAWDA, H.G., SUDKAR, A., BEHERE, I., KOTULKAR, M., SHAIKH, Z.M., KUMAT, A., BATULE, P., MISHRA, D. & SINGH, P.',2018,'Description of two new species of Aliinostoc and one new species of Desmonostoc from India based on the Polyphasic Approach and reclassification of Nostoc punensis to Desmonostoc punense comb. nov','FEMS Microbiology Letters 365: fny272',NULL,'https://doi.og/10.1093/femsle/fny272',0),(579,'SINGH, P., SHAKIH, Z.M., GAYSINA, L.M., SUDKAR, A. & SAMANTA, U.',2016,'New species of Nostoc (cyanobacteria) isolated from Pune, India, using morphological, ecological and molecular attributes','Plant Systematics and Evolution 302: 1381-1394',NULL,'https://10.1007/s00606-016-1337-z',0),(580,'LEE, N.-J., BANG, S.-D., KIM, T., KI, J.-S. & LEE, O.-M.',2021,'Pseudoaliinostoc sejongens gen. &amp; sp. nov. (Nostocales, Cyanobacteria) from floodplain soil of the Geum River in Korea based on polyphasic approach','Phytotaxa 479(1): 055-070',NULL,'https://doi.org/10.11646/phytotaxa.479.1.4',0),(581,'KABIRNATAJ, S., NEMATZADEH, G.A., TALEBI, A.F.. SARAF, A., SUDKAR, A., MEISAM, T. & SINGH, P.',2020,'Description of novel species of Aliinostoc, Desikacharya and Desmonostoc using a polyphasic approach','International Journal of Systematic and Evolutionary Bacteriology 70: <span dir=\'ltr\'>3413–3426</span>',NULL,'https://doi.irg/10.1099/ijsem.0.004188',0),(582,'CHAVADAR, M., SARAF, A., SURADKAR, A, MISHRA, D., KUMAR, N. & SINGH, P.',2021,'Constrictifilum karadense gen. et sp. nov., a new Nostocalean genus from Maharashtra, India','FEMS Microbiology Letters, 368, fnab057',NULL,'https://doi.org/10.1093/femsle/fnab057',0),(583,'RAHMATPOUR, N., HAUSER, D.A., NELSON, J.M., CHEN, P.Y., VILLARREAL A., J.C.A., HO, M.-Y. & LI, F.-W.',2021,'A novel thylakoid-less isolate fills a billion-year gap in the evolution of Cyanobacteria','Current Biology 31',NULL,'https://doi.org/10.1016/j.cub.2021.04.042',0),(584,'ALVARENGA, D.A., ANDREOTE, A.P.D., BRANCO, L.H.Z., DELBAJE, E., CRUX, R.B., VARANI, A, de M. & FIORE, M.F.',2021,'<em>Amazonocrinis nigriterrae</em> gen. nov., sp. nov., <em>Atlanticothrix silvestris</em> gen. nov., sp. nov. and <em>Dendronalium phyllosphericum</em> gen. nov., sp. nov., nostocacean cyanobacteria from Brazilian environments','International Journal of Systematic and Evolutionary Microbiology 71:004811',NULL,'https://doi.org/10.1099/ijsem.0.004811',0),(585,'JUNG, P., AZUA-BUSTOS, A., GONZALEZ-SILVA, C., MIKHAILYUK, T., ZABICKI, D., HOLZINGER, A., LAKATOS, M. & BÜDEL, B.',2021,'Emendation of the Coccoid Cyanobacterial Genus <em>Gloeocapsopsis </em>and Description of the New Species <em>Gloeocapsopsis diffluens</em> sp. nov. and <em>Gloeocapsopsis dulcis</em> sp. nov. Isolated From the Coastal Range of the Atacama Desert (Chile)','Fronties in Microbiology',NULL,'https://doi.org/10.3389/fmicb.2021.671742',0),(586,'SAMYLINA, O.S., , SINETOVA, M.A., KUPRIYANOVA, E.V., STARIKOV, A.Y., SUKHACHEVA, M.V. & TOUROVA, T.P.',2021,'Ecology and biogeography of the ‘marine Geitlerinema’ cluster and a description of Sodalinema orleanskyi sp. nov., Sodalinema gerasimenkoae sp. nov., Sodalinema stali sp. nov. and Baaleninema simplex gen. et sp. nov. (Oscillatoriales, Cyanobacteria)','FEMS Microbiology Ecology 97: fiab104',NULL,'https://doi.org/10.1093/femsec/fiab104',0),(587,'NOWRUZI, B. & SHALYGIN, S.',2021,'Multiple phylogenies reveal a true taxonomic position of Dulcicalothrix alborzica sp. nov. (Nostocales, Cyanobacteria)','Fottea 21(2): 235-246',NULL,'https://doi.org/10.5507/fot.2021.008',0),(588,'CAI, F., YU, G., LIU, Y., SUN, Y. & LI, R.',2021,'Description of two new species of Nostoc from China based on the polyphasic approach','Fottea 21(2): 259-271',NULL,'https://doi.org/10.5507/fot.2021.011',0),(589,'KIM, D.-H., CHOI, H.J., KI, J.-S. & LEE, O.-M.',2021,'Pinocchia daecheonga sp. nov. (Synechococcales, Cyanobacteria) isolated from a Daecheong Lake in Geum River, Republic of Korea','Phytotaxa 510(2): 135-147',NULL,'https://doi.org/10.11646/phytotaxa.510.2.2',0),(590,'TANG, J., LI, L., LI, M., DU, L., SHAH, M.M.R., WALERON, M.M., WALERON, M., WALERON, K.F. & DAROCH, M.',2021,'Description, Taxonomy, and Comparative Genomics of a Novel species, <em>Thermoleptolyngbya sichuanensis</em> sp. nov., Isolated From Hot Springs of Ganzi, Sichuan, China','Frontiers in Microbiology',NULL,'https://doi.org/10.3389/fmicb.2021.696102',0),(591,'HAUEROVÁ, R., HAUER, T., KAŠTOVSKÝ, J., KOMÁREK, J., LEPŠOVÁ-SKÁCELOVÁ, O. & MAREŠ, J.',2021,'<em>Tenebriella </em>gen. nov. – The dark twin of Oscillatoria','Molecular Phylogenetics and Evolution 165: 107293',NULL,'https://doi.org/10.1016/j.ympev.2021.107293',0),(592,'CHAKRABORTY, S., MARUTHANAYAGAM, V., ACHARI, A., PRAMANIK, A., JAISANKAR, P. & MUKHERJEE, J.',2021,'<em>Aerofilum fasciculatum</em> gen. nov., sp. nov. (Oculatellaceae) and<em> Euryhalinema pallustris</em> sp. nov. (Prochlorotrichaceae) isolated from an Indian mangrove forest','Phytotaxa 522(3): 165-186',NULL,'https://doi.org/10.11646/phytotaxa.522.3.1',0),(593,'BONTHOND, G., SHALYGIN, S., BAYER, T. & WEINBERGER, F.',2021,'Draft genome and description of <em>Waterburya agarophytonicola</em> gen. nov. sp. nov. (Pleurocapsales, Cyanobacteria): a seaweed symbiont','Antonie van Leeuwenhoek',NULL,'https://doi.org/10.1007/s10482-021-01672-x',0),(594,'WANG, Y., JIA. N., GENG, R., YU, G. & LI, R.',2021,'Phylogenetic insights into Chroococcus-like taxa (Chroococcales, Cyanobacteria), Describing Cryptochroococcus tibeticus gen. nov sp. nov. and Limnococcus fonticola sp. nov. from Quinghai-Tibet Plateau','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13205',0),(595,'AVERINA, S., POLYAKOVA, E., SENATSKAYA, E. & PINEVICH, A.',2021,'A new cyanobacterial genus Altericista and three species, A. laculadogae sp. nov, A. violacea sp. nov., and A. variichlora sp. nov., described using polyphasic approach.','Journal of Phycology 57: 1517-1529',NULL,'https://doi.org/10.1111/jpy.13188',0),(596,'ABDULLIN, S.R, NIKULIN, A.Y., BAGMET, V.B., NIKULIN, V.Y. & GONTCHAROV, A.A.',2021,'New cyanobacterium Aliterella vladivostokensis sp. nov. (Aliterellaceae, Chroococcidiopsidales), isolated from temperate monsoon climate zone (Vladivostok, Russia)','Phytotaxa 527(3): 221-233',NULL,'https://doi.org/10.11646/phytotaxa.527.3.7',0),(597,'RASOULI-DOGAHEH, S., KOMÁREK, J., CHATCHAWAN, T. & HAUER, T.',2022,'<em>Thainema </em>gen. nov. (Leptolyngbyaceae, Synechococcales): A new genus of simple trichal cyanobacteria isolated from a solar saltern environment in Thailand','PLoS ONE 17(1): e0261682',NULL,'https://doi.org/10.1371/journal.pone.0261682',0),(598,'PANOU, M. & GKELIS, S.',2022,'Unravelling unknown cyanobacteria diversity linked with HCN production','Molecular Phylogenetics and Evolution 166: 107322',NULL,'https://doi.org/10.1016/j.ympev.2021.107322',0),(599,'BERTHOLD, D.E., LEFLER, F.W. & LAUGHINGHOUSE, H.D.',2022,'Recognizing novel cyanobacterial diversity in marine benthic mats, with the description of Sirenicapillariaceae fam. nov., two new genera, <em>Sirenicapillaria </em>gen. nov. and <em>Tigrinifilum </em>gen. nov., and seven new species','Phycologia',NULL,'https://doi.org/10.1080/00318884.2021.2006589',0),(600,'KIM, D.-H., LEE, N.-J., YOON, S.-R., KIM, T., KI, J.-S. & LEE, O.-M.',2022,'<em>Porphyrosiphon annulatus</em> sp. nov. (Oscillatoriales, Cyanobacteria) isolated on moist soil in Suwon, Republic of Korea','Phytotaxa 532 (3): 288–300',NULL,'https://doi.org/10.11646/phytotaxa.532.3.6',0),(601,'DE ARAÚJO, V.L., DOS SANTOS, M.F., SCHNADELBACH, A.S., NUNES, J.M. DE C., FIORE, M.F. & CAIRES, T.A.',2022,'Expanding the occurrence of <em>Euryhalinema </em>(Leptolyngbyaceae, Cyanobacteria) to the Atlantic Ocean and description of <em>E. epiphyticum</em> sp. nov. on the Brazilian coast','Phytotaxa 532 (3): 246–258',NULL,'https://doi.org/10.11646/phytotaxa.532.3.3',0),(602,'MIKHAILYUK, T., VINOGRADOVA, O., HOLZINGER, A., GLASER, K., AKIMOV, Y. & KARSTEN, U.',2022,'<em>Timaviella dunensis</em> sp. nov. from sand dunes of the Baltic Sea, Germany, and emendation of <em>Timaviella edaphica</em> (Elenkin) O.M. Vynogr. &amp; Mikhailyuk (Synechococcales, Cyanobacteria) based on an integrative approach','Phytotaxa 532 (3): 192–208',NULL,'https://doi.org/10.11646/phytotaxa.532.3.1',0),(603,'JOHANSEN, J.R., GONZÁLEZ-RESENDIZ, L., ESCOBAR-SÁNCHEZ, V., SEGAL-KISCHINEVZKY, C., MARTÍNEZ-YERENA, J., HERNÁNDEZ-SÁNCHEZ, J., HERNÁNDEZ-PÉREZ, G. & LEÓN-TEJERA, H.',2021,'When will taxonomic saturation be achieved? A case study in <em>​Nunduva</em>​ and<em>​ Kyrtuthrix</em>​ (Rivulariaceae, Cyanobacteria)​​​​​​','Journal of Phycology 57: 1699-1720',NULL,'https://doi.org/10.1111/jpy.13201',0),(604,'MACHADO DE LIMA, N.M. & BRANCO, L.H.Z.',2020,'Biological soil crusts: new genera and species of Cyanobacteria from Brazilian semi-arid regions','Phytotaxa 470 (4): 263–281',NULL,'https://doi.org/10.11646/phytotaxa.470.4.1',0),(605,'FERNANDES, V.M.C., GIRALDO-SILVA, A., ROUSH, D. & GARCIA-PICHEL, F.',2021,'Coleofasciculaceae, a monophyletic home for <em>​Microcoleus steenstrupii</em>​ complex and other desiccation-tolerant filamentous Cyanobacteria​​​','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13199',0),(606,'TANG, J., DU, L.-M., LI, M., YAO, D., JIANG, Y, WALERON, M., WALERON, K. & DAROCH, M.',2022,'Characterization of a Novel Hot-Spring Cyanobacterium <em>Leptodesmis sichuanensis</em> sp. Nov. and Genomic Insights of Molecular Adaptations Into Its Habitat','Frontiers in Microbiology 12: 739625',NULL,'https://doi.org/10.3389/fmicb.2021.739625',0),(607,'MOLINARI-NOVOA, E.A., MAYATA, L.F., SÁNCHEZ OCHARAN, C.E. & GUIRY, M.D.',2021,'Nomenclatural notes on algae. I. Replacement names for various algal taxa','Notulae Algarum 177',NULL,'https://notulaealgarum.org/2021/documents/Notulae%20algarum%20No.%20177.pdf',0),(608,'TAWONG, W., PONGCHAROEN, P., PONGPADUNG, P. & PONZA, S.',2020,'Validation of “Neowollea manoromensis” Tawong, nom. inval. (Cyanophyta, Nostocaceae) from Thailand','Notulae Algarum No. 214',NULL,'https://notulaealgarum.org/2021/documents/Notulae%20algarum%20No.%20214.pdf',0),(609,'KOZLÍKOVÁ-ZAPOMĚLOVÁ, E., CHATCHAWAN, T., KAŠTOVSKÝ, J. & KOMÁREK J.',2016,'Phylogenetic and taxonomic position of the genus Wollea with the description of Wollea salina sp. nov. (Cyanobacteria, Nostocales)','Fottea 16(1): 43-55',NULL,'https://doi.org/10.5507/fot.2015.026',0),(610,'JURÁŇ, J., HAUER, T., JOHANSEN, J.R. & KRIENITZ, L.',2015,'(2365) Proposal to conserve the name <em>Cyanospira </em>G. Florenz. &amp; al. (Cyanophyceae) against <em>Cyanospira </em>Chodat (Euglenophyceae)','Taxon 64(4): 845–846',NULL,'http://dx.doi.org/10.12705/644.17',0),(611,'SOARES, F., TROVAO, J., AHN, A.-C., WILMOTTE, A., CARDOSO, S.M., TIAGO, I. & PORTUGAL, A.',2022,'Introducing Petrachlorosaceae fam. nov., <em>​Petrachloros </em>​gen. nov. and <em>​Petrachloros mirabilis</em>​ sp. nov. (Synechococcales, Cyanobacteria) isolated from a Portugese UNESCO monument​​​​​​​ ​​​','Journal of Phycology 58: 219-233',NULL,'https://doi.org/10.1111/jpy.13241',0),(612,'BRITO, A., ROCHA, M., KAŠTOVSKÝ, J., VIEIRA, J., VIEIRA, C.P., RAMOS, V., CORREIA, M., SANTOS, M., MOTA, R., ROQUE, J., PISSARRA, J., MELO, P. & TAMAGNINI, P.',2022,'A new cyanobacterial species with a protective effect on lettuce grown under salinity stress: Envisaging sustainable agriculture practices','Journal of Applied Phycology 34: 915-928',NULL,'https://doi.org/10.1007/s10811-022-02692-4',0),(613,'CAI, F., LI, S., ZHANG, H., YU, G. & LI, R.',2022,'Nodosilinea hunanesis sp. nov. (Prochlorotrichaceae, Synechococcales) from a Freshwater Pond in China Based on a Polyphasic Approach','Diversity',NULL,'http://dx.doi.org/10.3390/d14050364',0),(614,'CAI, F., YU, G. & LI, R.',2022,'Description of two new species of Pseudoaliinostoc (Nostocales, Cyanobacteria) from China based on the polyphasic approach','Journal of Oceanology and Limnology',NULL,'https://doi.org/10.1007/s00343-021-1111-0',0),(615,'TAWONG, W-, PONGCHAROEN, P. & NISHIMURA, T.',2022,'Geosmin–producing <em>Scytonema foetidum</em> sp. nov. (Scytonemataceae, Cyanobacteria): morphology and molecular phylogeny','Fottea 22(1): 78-92',NULL,'https://doi.org/10.5507/fot.2021.017',0),(616,'GAYSINA, L.A., JOHANSEN, J.R., SARAF, A., ALLAGUVATOVA, R.Z., PAL, S. & SINGH, P.',2022,'<em>Roholtiella volcanica</em> sp. nov., a New Species of Cyanobacteria from Kamchatkan Volcanic Soils','Diversity 14:220',NULL,'https://doi.org/10.3390/d14080620',0),(617,'GÄRTNER-STOYNEVA, M.P., GÄRTNER, G., UZUNOV, B., DESCY, J.-P. & OKELLO, W.',2022,'<strong>Cyanocystopsis kitagatae</strong> gen. et sp. nov. (Cyanoprokaryota/Cyanobacteria) from the tropical lake Kitagata (Uganda, Africa)','Wulfenia 28: 51:65',NULL,'',0),(618,'JUNG, P., SOMMER, V., KARSTEN, U. & LAKATOS, M.',2022,'Salty Twins: Salt-Tolerance of Terrestrial <em>Cyanocohniella </em>Strains (Cyanobacteria) and Description of <em>C. rudolphia</em> sp. nov. Point towards a Marine Origin of the Genus and Terrestrial Long Distance Dispersal Patterns','Microorganisms 10: 968',NULL,'https://doi.org/10.3390/microorganisms10050968',0),(619,'LEE, N.-J., KIM, T., KIM, D.-H., KI, J.-S. & LEE, O.-M.',2022,'<em>Edaphophycus epilithus</em> gen. et sp. nov. (Oscillatoriales, cyanobacteria) with a description of the morphology and molecular phylogeny','Phycological Research',NULL,'https://doi.org/ 10.1111/pre.12499',0),(620,'BALDARELLI, L.M., PIETRASIAK, N., OSORIO-SANTOS, K. & JOHANSEN, J.R.',2022,'<em>​Mojavia aquilerae </em>​and<em>​ M. dolomitesstris</em>​ - two new Nostocaceae (Cyanobacteria) species from the Americas​​​​​​','Journal of Phycology 58: 502-516',NULL,'https://doi.org/10.1111/jpy.13275',0),(621,'MOLINARI-NOVOA, E.A. & GUIRY, M.D.',2021,'Nomenclatural notes on algae. IV. Further replacement names for various algal taxa','Notulae Algarum 183',NULL,'https://notulaealgarum.org/2021/documents/Notulae%20algarum%20No.%20183.pdf',0),(622,'SHEN, L.-Q., ZHANG, Z.-C., SHANG, J.-L., LI, Z.-K., CHEN, M., LI, R. & QIU, B.-S.',2022,'<em>​Kovacikia minuta</em>​ sp. nov. (Leptoplyngbyaceae, Cyanobacteria), a new freshwater chlorophyll F proproducing Cyanobacterium​​​','Journal of Phycology 58: 424-435',NULL,'https://doi.org/10.1111/jpy.13248',0),(623,'CHRISTODOULOU, M., JOKELA, J., WAHLSEN, M., SAARI, L., ECONOMOU-AMILI, A., FIORE, M.F. & SIVONEN, K.',2022,'Description of Aliinostoc alkaliphilum sp. nov. (Nostocales, Cyanobacteria), a New Bioactive Metabolite-Producing Strain from Salina Verde (Pantanal, Brazil) and Taxonomic Distribution of Bioactive Metabolites in Nostoc and Nostoc-like Genera','Water 14: 2470',NULL,'https://doi.org/10.3390/w14162470',0),(624,'TAWONG, W., PONGCHAROEN, P., NISHIMURA, T. & SAIJUNTHA, W.',2022,'<em>Siamcapillus rubidus</em> gen. et sp. nov. (Oculatellaceae), a novel filamentous cyanobacterium from Thailand based on molecular and morphological analyses','Phytotaxa 558 (1): 033–052',NULL,'https://doi.org/10.11646/phytotaxa.558.1.2',0),(625,'JASSER, I., PANOU, M., KHOMOUTOVSKA, N., SANDZEWICZ, M., PANTERIS. E., NIYATBEKOV, T., LACH, L., KWIATKOWSKI, J., KOKOCIŃSKI, M. & GKELIS, S.',2022,'Cyanobacteria in hot pursuit: Characterization of cyanobacteria strains, including novel taxa, isolated from geothermal habitats from different ecoregions of the world','Molecular Phylogenetics and Evolution 170: 107454',NULL,'https://doi.org/10.1016/j.ympev.2022.107454',0),(626,'CONKLIN, K.Y., STANCHEVA, R., OTTEN, T.G., FADNESS, R., BOYER, G.L., READ, B., ZHANG, X. & SHEATH, R.G.',2020,'Molecular and morphological characterization of a novel dihydroanatoxin-a producing Microcoleus species (cyanobacteria) from the Russian River, California, USA','Harmful Algae 93: 101767',NULL,'https://doi.org/10.1016/j.hal.2020.101767',0),(627,'JUNG, P., BRUST, K., SCHULTZ, M., BÜDEL, B., DONNER, A. & LAKATOS, M.',2021,'Opening the Gap: Rare Lichens With Rare Cyanobionts – Unexpected Cyanobiont Diversity in Cyanobacterial Lichens of the Order Lichinales','Frontiers in Microbiology 12: 728378',NULL,'https://doi.org/10.3389/fmicb.2021.728378',0),(628,'PAL, S., SARAF, A., KUMAR, N., SINGH, A., TALUKDAR, U., KOHAR, N. & SINGH, P.',2022,'Digging deeper into the taxonomy of <em>Cylindrospermum </em>and description of<em> Johanseniella tripurensis</em> gen. et sp. nov. from India','FEMS Microbiology Letters 369: 1–9',NULL,'https://doi.org/10.1093/femsle/fnac074',0),(629,'TANG, J., SHAH, M.R., YAO, D., JIANG, Y., DU, L., ZHAO, K., LI, L., WALERON, M.M., WALERON, M., WALERON, K. & DAROCH, M.',2022,'Polyphasic Identification and Genomic Insights of <em>Leptothermofonsia sichuanensis</em> gen. sp. nov., a Novel Thermophilic Cyanobacteria Within Leptolyngbyaceae','Frontiers in Microbiology 13: 765105',NULL,'https://doi.org/10.3389/fmicb.2022.765105',0),(630,'ZAPOMĚLOVÁ, E., JEZBEROVÁ, J., ŘEHÁKOVÁ, K. & KOMÁRKOVÁ J.',2009,'Polyphasic characterization of three strains of <em>​Anabaena reniformis</em>​ and <em>​Aphanizomenon aphanizomenoides</em>​ (Cyanobacteria) and their reclassification to <em>​Sphaerospermum</em>​ gen. nov. (incl. <em>​Anabaena kisseleviana</em>​)​​​​​​​​​​​​','Journal of Phycology 45: 1363-1373',NULL,'hrrps://doi.org/10.1111/j.1529-8817.2009.00758.x',0),(631,'PAL, S., SARAF, A., KUMAR, N. & SINGH, P.',2022,'Phycological exploration of the global biodiversity hotspots of Northeast India: discovery of a new species of soil-dwelling cyanobacteria, <em>Desikacharya kailashaharensis</em> sp. nov.','FEMS Microbiology Letters 369: 1-10',NULL,'https://doi.org/10.1093/femsle/fnac099',0),(632,'BERTHOLD, D., WERNER, V.R., LEFLER, F.W., SIMON, I.P. & LAUGHINGHOUSE IV., H.D.',2022,'The novel marine cyanobacterium <em>Nunduva sanctimaloensis</em> sp. nov. (Nostocales, Cyanobacteria) from rocky shores and its reproduction through modified monocytes','Fottea 22(2): 192-203',NULL,'https://doi.org/10.5507/fot.2021.023',0),(633,'KUMAR, N., SARAF, A., PAL, S., MISHRA, D., SINGH, P. & JOHANSEN, J.R.',2022,'Circumscription of Fulbrightiella gen. nov. and Sherwoodiella gen. nov, two novel genera in the Calotrichaceae (Nostocales, Cyanobacteria)','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13297',0),(634,'LUKEŠOVÁ, A., JOHANSEN, J.R., MARTIN, M.P. & CASAMATTA, D.A.',2009,'<em>Aulosira bohemensis</em> sp. nov.: further phylogenetic uncertainty at the base of the Nostocales (Cyanobacteria)','Phycologia 48(2): 118-129',NULL,'https://doi.org/10.2216/08-56.1',0),(635,'STRUNECKÝ, O., IVANOVA, A.P. & MAREŠ, J.',2023,'An updated classification of cyanobacterial orders and families based on phylogenomic and polyphasic analysis','Journal of Phycology',NULL,'https://doi.org/10.1111/jpy.13304',0),(636,'STRUNECKÝ, O., RAABOVÁ, L., BERNARDOVÁ, A., IVANOVA, A.P., SEMANOVÁ, A., CROSSLEY, J. & KAFTAN, D.',2020,'Diversity of cyanobacteria at the Alaska North Slope with description of two new genera: Gibliniella and Shackletoniella','FEMS Microbiology Ecology 96(3): fiz189',NULL,'https://doi.org/10.1093/femsec/fiz189',0),(637,'MALTSEVA, S., KEZLYA, E., KRIVOVA, Z., GUSEV, E., KULIKOVSKIY, M. & MALTSEV, Y.',2022,'Phylogeny and fatty acid profiles of Aliinosotc vietnamicum sp. nov. (Cyanobacteria) from the soils of Vietnam','Journal of Phycology 58: 789-803',NULL,'https://doi.org/10.1111/jpy.13283',0);
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Journal of Phycology 50: 1094&nbsp;',9,'[73]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(32,'Hapalosiphonaceae','Elenkin',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(33,'Microchaetaceae','Lemmermann',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(34,'Nostocaceae','Eichler',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(35,'Nostochopsidaceae','Geitler',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-07-19 12:19:57','admin'),(36,'Rivulariaceae','Bornet et Flahault',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(37,'Scytonemataceae','Rabenhorst et al.',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(38,'Stigonemataceae','Bornet et al.',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(39,'Symphyonemataceae','Hoffman et al.',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(40,'Tolypotrichaceae','Hauer, Bohunická, Johansen, Mareš et Berrendero-Gómez 2014. Journal of Phycology 50: 1093',9,'[73]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2022-03-22 13:59:07','admin'),(41,'Ammatoideaceae','Elenkin',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-05 14:04:59','admin'),(42,'Borziaceae','Borzì',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(43,'Camptothricaceae','West et West',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(44,'Coleofasciculaceae','Komárek et al. 2014',2554,'[1][605]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:30:27','admin'),(45,'Cyanothecaceae','Komárek et al. 2014',2559,'[1]',NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:42:38','admin'),(46,'Desertifilaceae','Hašler et al. 2017. Phycologia 56(3): 287',2552,'[289]','','Family',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:22:50','admin'),(47,'Gomontiellaceae','Elenkin ex Geitler',2559,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:43:55','admin'),(48,'Homoeotrichaceae','',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(49,'Microcoleaceae','Strunecký et al. 2013. Journal of Phyclogy 49: 1176',10,'[334]','','Family',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(50,'Oscillatoriaceae','Engler',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(51,'Phormidiaceae','Anagnostidis et Komárek',10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(52,'Dermocarpellaceae','Christensen',11,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(53,'Hydrococcaceae','Kützing',11,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(54,'Hyellaceae','Borzì',11,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(55,'Xenococcaceae','Ercegovic',11,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(56,'Spirulinaceae','(Gomont) Hoffmann et al.',12,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(57,'Acaryochloridaceae','Komárek et al. 2014',2530,'[1]','invalid nominate genus','Family',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2023-01-31 08:31:08','admin'),(58,'Chamaesiphonaceae','Borzì',2559,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:45:03','admin'),(59,'Coelosphaeriaceae','Elenkin',13,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(60,'Heteroleibleiniaceae','(Komárek et Anagnostidis) Komárek et al. 2014',13,'[1]',NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(61,'Leptolyngbyaceae','(Komárek et Anagnostidis) Komárek et al. 2014',2548,'[1]',NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:28:53','admin'),(62,'Merismopediaceae','Elenkin',13,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(63,'Prochloraceae','Lewin',6,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:25:42','admin'),(64,'Pseudanabaenaceae','Anagnostidis et Komárek',2333,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-28 06:41:54','admin'),(65,'Romeriaceae','Komárek et al. 2014',13,'[1]',NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(66,'Synechococcaceae','Komárek et Anagnostidis',13,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(67,'Anabaenoideae',NULL,34,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(68,'Aphanothecoideae',NULL,16,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(69,'Entophysalidoideae',NULL,19,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(70,'Gomontielloideae',NULL,47,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(71,'Gomphosphaerioideae',NULL,20,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(72,'Heteroleibleinioideae',NULL,60,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(73,'Hormoscilloideae',NULL,47,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(74,'Hyelloideae',NULL,54,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(75,'Mastigocladoideae',NULL,96,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-12 05:38:16','admin'),(76,'Merismopedioideae',NULL,1,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(77,'Microchaetoideae',NULL,33,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(78,'Microcoleoideae',NULL,49,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(80,'Nostocoideae',NULL,34,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(81,'Oscillatorioideae',NULL,50,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(82,'Pascherinematoideae',NULL,54,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(83,'Phormidioideae',NULL,51,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(84,'Plectonematoideae',NULL,50,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(85,'Podocapsoideae',NULL,54,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(86,'Pseudanabaenoideae',NULL,64,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(87,'Siphononematoideae',NULL,19,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(88,'Solentioideae',NULL,54,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(89,'Synechococcoideae',NULL,66,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(90,'Tolypotrichoideae',NULL,33,NULL,NULL,'Subfamily/Tribe',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(91,'Borzinemataceae',NULL,9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(92,'Fischerellaceae',NULL,9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-07-16 05:08:10','admin'),(93,'Loriellaceae',NULL,9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-07-19 12:14:36','admin'),(94,'Schizothrichaceae',NULL,10,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(96,'Mastigocladaceae','',9,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-07-19 12:17:38','admin'),(97,'Acaryochloris','Miyashita et Chihara in Miyashita, Ikemoto, Kurano, Miyachi et Chihara 2003. Journal of Phycology 39: 1249',8,'','','Genus',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(98,'Adrianema','De Toni 1936. Noterelle di nomenclura algologica VIII.: 2',39,'','','Genus','[2]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(99,'Albrightia','Copeland 1936. Ann. New York Acad. Sci. 36: 85.',32,NULL,NULL,'Genus','[3]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(100,'Alternantia','Schiller, 1954. Oesterr. Acad. Wiss., Math.-Nat. Kl., Sitzungsber., Abt. 1, Biol. 163: 134.',65,'','','Genus','[4]','','','',NULL,NULL,0,1,'',0,'active','2023-01-31 07:51:36','admin'),(101,'Ammatoidea','W. et G.S. West, 1897. J. Roy. Microsc. Soc. London 1897: 506.',48,NULL,NULL,'Genus','[5]',NULL,NULL,NULL,NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(102,'Anabaena','Bory ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 224.',34,NULL,NULL,'Genus','[6]','[11][25][26][52][65][165][181]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(103,'Anabaenopsis','(Woloszyńska) Miller 1923. Arch. Russk. Protistol. 2: 125.',25,NULL,NULL,'Genus','[7][8]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-26 10:53:54','admin'),(104,'Aphanizomenon','Morren ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 241.',25,NULL,NULL,'Genus','[9]','[110][111]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(105,'Aphanocapsa','Nägeli, 1849. Gattungen einzelliger Algen: 52.',62,'[115]','','Genus','[10]','[17]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-05-24 05:04:32','admin'),(106,'Aphanothece','Nägeli 1849, nom. cons., Gattungen einzelliger Algen: 59',15,'','','Genus','[11]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(107,'Arthronema','Komárek et Lukavský, 1988. Algolog. Stud. 50-53: 266.',61,NULL,NULL,'Genus','[12]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:29:23','admin'),(108,'Arthrospira','Stitzenberger ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 246.',49,NULL,NULL,'Genus','[13]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(109,'Asterocapsa','Chu,1952. Ohio J. Sci. 52: (2): 97.',16,'[386]','','Genus','[14]','[12]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-06 05:10:26','admin'),(110,'Aulosira','Kirchner ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 256.',34,'','','Genus','[15]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(111,'Bacularia','Borzì, 1905. Nuova Notarisia 16: 21.',65,NULL,NULL,'Genus','[16]','[23]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:51:08','admin'),(112,'Baradlaia','Palik 1960. Ann. Univ. Sci. Budapest Sect. Biol. 3: 283.',32,NULL,NULL,'Genus','[17]',NULL,NULL,NULL,'Wall in a limestone cave','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(113,'Blennothrix','Kützing ex Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 429.',50,NULL,NULL,'Genus','[19]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(114,'Borzia','Cohn ex Gomont 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 198.',42,NULL,NULL,'Genus','[20]',NULL,NULL,NULL,NULL,NULL,1,1,NULL,0,'active','2019-06-06 06:30:59','admin'),(115,'Borzinema','De Toni 1936. Noter. Nomencl. Algol. 8: 2.',40,NULL,NULL,'Genus','[21]','[63]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(116,'Brachytrichia','Zanardini ex Bornet et Flahault 1887. Ann. Sci. Nat. Bot., ser. 7, 4: 371.',39,NULL,NULL,'Genus','[22]','[88]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(117,'Brachytrichiopsis','Jao 1944. Sinensia 15: 78',32,'[450]','','Genus','[23]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-10-08 04:51:38','admin'),(118,'Brasilonema','Fiore, Sant\'Anna, Azevedo, Komárek, Kaštovský, Sulek et Lorenzi, 2007. J. Phycol. 43:794',37,NULL,NULL,'Genus','',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-04-09 02:01:49',NULL),(119,'Calothrix','Agardh ex Bornet et Flahault, 1886. Ann. Sci. Nat. Bot., ser. 7, 3: 345.',1961,NULL,NULL,'Genus','[39]','[57][104][116][122][121][147][149]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-12-05 09:08:57','admin'),(120,'Camptylonemopsis','Desikachary 1948. Proc. Indian Acad. Sci., Sect. B. 18: 46.',33,NULL,NULL,'Genus','[40]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(121,'Capsosira','Kützing ex Bornet et Flahault, 1888. Ann. Sci. Nat. Bot., ser. 7, 5: 79.',26,NULL,NULL,'Genus','[41][65]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(122,'Chamaecalyx','Komárek et Anagnostidis, 1986. Algolog. Stud. 38-39: 199.',54,NULL,NULL,'Genus','[52]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(123,'Chamaesiphon','A. Braun et Grunow, 1865. – In Rabenhorst, Algen Eur. Decaden 72/73: 1726. - nomen conservandum',58,'','Several species (<em>Chamaesiphon subglobosus</em>, <em>C. polonicus</em>) are cultured as mono specific strains. In this case they grow in irregular groups, not forming characteristic colonies, <em>C. subglobosus</em> sometimes without sheaths (fig. 487). The heteropolarity is manifested in culture usually only by asymmetric cell division. (Komárek &amp; Anagnostidis, 1998)','Genus','[53]','[29][79][92][35][161]','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(124,'Chlorogloea','Wille, 1900. Nytt. Mag. Naturvidensk. 38: 5.',19,NULL,NULL,'Genus','[56]','[119][184]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(125,'Chlorogloeopsis','Mitra et Pandey 1967. Phykos 5: 112.',27,NULL,NULL,'Genus','[55]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(126,'Chondrogloea','Schmidle 1901. In Engler, Bot. Jahrb. Syst. 30: 247.',32,NULL,NULL,'Genus','[58]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:17:29','admin'),(127,'Chroococcidiopsis','Geitler, 1933. Arch. Hydrobiol., Suppl. 12: 625.',55,NULL,'Often overlooked and misinterpreted.','Genus','[59]','[12]',NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(128,'Chroococcidium','Geitler, 1933. Arch. Hydrobiol., Suppl. 12: 624.',55,NULL,NULL,'Genus','[60]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(129,'Chroococcopsis','Geitler, 1925. Arch. Protistenk. 51: 342.',55,NULL,'Four described, not well known species. Probably more taxa.','Genus','[61]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(130,'Chroococcus','Nägeli,1849. Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss. 10(7): 45.',16,NULL,'Variable genus; about 60 definable species from more than 120 described.','Genus','[62]','[146]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(131,'Chroogloeocystis','Brown, Mummey et Cooksey, 2005. FEMS Microbiology Ecology 52: 310-310',23,'[166]','no formal description in the paper','Genus','[24][25][26][27]','','','',NULL,NULL,0,0,NULL,0,'active','2023-02-01 13:46:39','admin'),(132,'Clastidium','Kirchner, 1880. Jahresh. Ver. Vaterl. Naturk. Württemb. 36: 196.',58,NULL,'Four species','Genus','[64]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(133,'Coccopedia','Troickaja, 1922. Bot. Mater. Inst. Sporov. Rast. Glavn. Bot. Sada RSFSR 1:131.',62,NULL,'Two species','Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(134,'Coelomoron','Buell, 1938. Bull. Torrey Bot. Club 65: 379.',59,'','','Genus','[66]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(135,'Coelosphaeriopsis','Lemmermann, 1900. Abh. Nat. Ver. Bremen 16: 352.',71,NULL,'Two not revised species','Genus','[67]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(136,'Coelosphaerium','Nägeli, 1849. Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss. 10(7): 54.',71,NULL,'From more than 20 described species about 10 are probably valid and occasionally cited in papers, but only 4 are well known.','Genus','[68]','[41][91][135]',NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(137,'Coleodesmium','Borzì ex Geitler 1942. In Engler et Prantl, Nat. Pflanzenfam., 2. Ed., 1b: 154.',40,NULL,'Seven species, from which three need revision. All taxa need further studies.','Genus','[69]','[19][42][44][43][58]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(138,'Colteronema','Copeland 1936. Ann. N. Y. Acad. Sci. 36: 79.',32,NULL,'Monospecific genus','Genus','[70]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:12:50','admin'),(139,'Crinalium','Crow, 1927. Ann. Bot. (London) 41: 165.',47,NULL,NULL,'Genus','[126]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(140,'Crocosphaera','Zehr, Rachel A.Foster, Waterbury et E.Webb in Mareš et al. 2019. Journal of Phycology 55: 601',15,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-30 09:31:02','admin'),(141,'Cronbergia','Komárek, Zapomělová et Hindák, 2010. Cryptogamie, Algologie 31(3): 329',34,'[164]','','Genus','[130]','','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(142,'Cuspidothrix','Rajaniemi, Komárek, Willame, Hrouzek, Kaštovská, Hoffmann et Sivonen, 2005. Arch. Hydrobiol./Algol. Stud. 117: 388',25,NULL,NULL,'Genus','[139][140]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-10-06 06:18:41','admin'),(143,'Cyanoarbor','Wang, 1989. Acta phytotax. sinica 27(2): 129-131.',19,NULL,NULL,'Genus','[143]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-06 14:39:45','admin'),(144,'Cyanobacterium','Rippka et Cohen-Bazire, 1983. Ann. Microbiol. (Inst. Pasteur) 134B: 32.',16,'','','Genus','[144]','',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2019-06-10 04:03:09','admin'),(145,'Cyanobium','Rippka et Cohen-Bazire 1983',416,'[574]','','Genus','[145]','',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2021-05-28 06:37:01','admin'),(146,'Cyanobotrys','L. Hoffman, 1991. Algolog. Stud. 64: 349.',38,NULL,'Monotypic genus','Genus','[147]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(147,'Cyanocatena','Hindák, 1975. Arch. Hydrobiol., Suppl. 46: 334.',16,NULL,'Monotypic genus.','Genus','[148]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-10 04:28:21','admin'),(148,'Cyanocatenula','Joosten, <em>2006</em>. Flora of the Blue-green algae of the Netherlands I., p. 207',2545,'','','Genus','','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:38:14','admin'),(149,'Cyanocomperia','Hindák, 2002. Nova Hedwigia, Beih. 123: 81',21,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(150,'Cyanocystis','Borzi, 1882. Nuovo Giorn. Bot. Ital. 14: 314.',52,NULL,'About 16 species','Genus','[151]','[159]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(151,'Cyanoderma','Weber van Bosse 1887. Nat. Verh. Holl. Maatsch. Wetensch. Haarlem, ser. 3, 5: 18',54,NULL,NULL,'Genus','[200]','[75][129][145]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(152,'Cyanodermatium','Geitler, 1933. Arch. Hydrobiol., Suppl.12: 627',53,NULL,'Two species, very little known.','Genus','[152]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(153,'Cyanodictyon','Pascher 1914. Ber. Deutsch. Bot. Ges. 32: 351.',66,NULL,NULL,'Genus','','[160]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(154,'Cyanogranis','Hindák,1982. Algolog. Stud. 32: 244.',16,NULL,'Two species','Genus','[154]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-10 04:42:58','admin'),(155,'Cyanokybus','Schiller, 1956. In Gessner et Vareschi, Ergebn. Deutsch. Limnol. Venezuela-Exped. 1952, p. 202.',16,NULL,'Monospecific genus.','Genus','[155]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(156,'Cyanonephron','Hickel, 1985. Algolog. Stud. 38-39: 100.',66,NULL,NULL,'Genus','',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(157,'Cyanophanon','Geitler, 1955. Österr. Bot. Zeitschr. 102: 269.',58,NULL,'Two species','Genus','[157]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(158,'Cyanosaccus','Lukas et Golubić 1981. Journal of Phycology 17: 225.',54,'[149]','','Genus','[158]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(159,'Cyanosarcina','Kováčik 1988. Algolog. Stud. 50-53: 175.',16,NULL,'Eight to ten species','Genus','[159]','[12][70]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(160,'Cyanospira','Florenzano, Sili, Pelosi et Vincenzini 1985. Archives of Microbiology 140: 305 nom. illeg.',25,'','name Cyanospira was used earlier by Chodat (1921) for different organism','Genus',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','2019-07-26 10:53:31','admin'),(161,'Cyanostylon','Geitler, 1928. Arch. Protistenk. 60: 441',16,NULL,NULL,'Genus','[160]','[173]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(162,'Cyanotetras','Hindák, 1988. Preslia 60: 291.',62,NULL,'Three species.','Genus','[161]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(163,'Cyanothamnos','Cronberg, 1991. Algolog. Stud. 64: 63-65.',66,NULL,'Monotypic genus','Genus','[162]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(164,'Cyanothece','Komárek, 1976. Arch. Protistenk. 118: 146.',45,'[397]','','Genus','[163]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:42:22','admin'),(165,'Cylindrospermopsis','Seenayya et Subba Raju, 1972. Tax. Biol. Blue-green Alg. (Madras), p. 55.',25,NULL,NULL,'Genus','[164][174][173][177][165][169][170][175][179][180][181]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-10-11 07:41:01','admin'),(166,'Cylindrospermum','Kützing ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 249.',34,'[452]','About 50 species, several need revision.','Genus','[182]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-10-08 12:01:34','admin'),(167,'Dalmatella','Ercegović, 1929. Acta Bot. Inst. Bot. Univ. Zagreb. 4: 39.',53,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(168,'Dasygloea','Thwaites ex Gomont, 1892. Ann. Sci. Nat.-Bot. 7, 15: 346.',430,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(169,'Dermocarpella','Lemmermann, 1907. Bot. Jahrb. Syst. 38: 349.',52,NULL,'Six species','Genus','[184]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(170,'Desmosiphon','Borzi, 1907. Atti Congr. Nat. Ital. Milano 1906: 372.',26,'','','Genus','[185]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 12:35:55','admin'),(171,'Dichothrix','Zanardini ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 3: 373',36,NULL,NULL,'Genus','[186]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(172,'Dolichospermum','(Ralfs ex Bornet et Flahault) Wacklin, Hoffmann et Komárek, 2009. Fottea 9(1): 60',25,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(173,'Doliocatella','Geitler 1933. Arch. Hydrobiol., Suppl. 12: 630.',38,'','','Genus','[187]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 12:42:53','admin'),(174,'Dzensia','Voronichin, 1929. Izv. Glavn. Bot. Sada SSSR 28: 158.',15,'','','Genus','[188]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 12:44:38','admin'),(175,'Entophysalis','Kützing 1843. Phycologia generalis: 177.',19,'[135]','','Genus','[189]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(176,'Epigloeosphaera','Komárková-Legnerová 1991. Algological Studies 62: 10-11.',66,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(177,'Epilithia','Ercegović, 1932. Rad Jugoslav. Akad. Znan. 244: 141.',53,'','','Genus','[191]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 12:50:35','admin'),(178,'Ercegovicia','de Toni 1936',54,NULL,NULL,'Genus',NULL,'[28]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(179,'Eucapsis','Clements et Shantz, 1909. Minn. Bot. Stud. 4: 134.',21,NULL,NULL,'Genus','[192]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(180,'Fischerella','(Bornet et Flahault) Gomont, 1895. J. Bot. 9: 52.',32,NULL,'About 15 species, from which only several are well known (and were isolated in cultures).','Genus','[194]','[72][156]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(181,'Fischerellopsis','Fritsch 1932. J. Bot. 70: 129.',32,NULL,'Two or three species; generic position and generic features need revision.','Genus','[195]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 12:56:04','admin'),(182,'Fortiea','De Toni 1936. Noter Nomencl. Algol. 8: 3.',29,'[73]','','Genus','[196]','[108]','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(183,'Gardnerula','De Toni, 1936. Noter. Nomencl. Algol. 8: 5.',36,NULL,NULL,'Genus','[197]','[139]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(184,'Geitleria','Friedmann 1955. Bot. Notiser 108: 444.',1066,'[488]','','Genus','[198]','','','',NULL,NULL,0,1,'',0,'active','2020-01-14 16:26:35','admin'),(185,'Geitleribactron','Komárek, 1975. Plant Syst. Evol. 123: 276',58,'[130][131]','Two species.','Genus','[199]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(186,'Geitlerinema','(Anagnostidis et Komárek) Anagnostidis, 1989. Plant. Syst. Evol. 164: 33-46.',2551,'[182]','','Genus','[201]','','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:21:07','admin'),(187,'Geminocystis','Korelusová, Kaštovský et Komárek 2009. Journal of Phycolology 45:933.',2287,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 12:29:12','admin'),(188,'Glaucospira','Lagerheim, 1892. Ber. Deutsch. Bot. Ges. 10(1): 365.',56,NULL,NULL,'Genus','[202]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-11 05:27:31','admin'),(189,'Gloeobacter','Rippka, Waterbury et Cohen-Bazire 1974. Archives for Microbiology 100: 435 nom. cons.',24,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(190,'Gloeocapsa','Kützing, 1843, nom. cons. Phycol. gen., p. 173.',23,'','','Genus','','[27][124][157][178]','','',NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:47:09','admin'),(191,'Gloeocapsopsis','Geitler, 1925. Beih. Bot. Centralbl. 2, 41: 229.',23,NULL,NULL,'Genus','[205]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:47:17','admin'),(192,'Gloeothece','Nägeli, 1849. Gattungen der einzelliger Algen: 57',16,'[115][536]','typus conservandum Gloeothece fuscolutea','Genus','[206]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-04-16 09:34:11','admin'),(193,'Gloeotrichia','J. Agardh ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 4: 365.',30,NULL,NULL,'Genus','[207]','[74][36][114][140]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-16 05:07:16','admin'),(194,'Gomontiella','Teodoresco, 1901. Verh. Zool.-Bot. Ges. Wien 51: 757.',47,NULL,NULL,'Genus','[208]','[48]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(195,'Gomphosphaeria','Kützing, 1836. Algarum Aquae Dulcis German. 16: 3.',71,NULL,NULL,'Genus','[209]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(196,'Halomicronema','Abed, Garcia-Pichel et Hernández-Mariné, 2002 Arch. Microbiol. 177: 368',416,'','','Genus','[211]','','','',NULL,NULL,0,0,'',0,'active','2023-01-31 07:29:00','admin'),(197,'Halothece','(Garcia-Pichel, Nübel et Muyzer) Margheri, Ventura, Kaštovský et Komárek, 2008. Phycologia 47 (5): 480',2558,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:32:58','admin'),(198,'Handeliella','Skuja in Handel-Mazzetti, 1937. Symb. Sinicae 1: 30.',32,NULL,NULL,'Genus','[215]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(199,'Hapalosiphon','Nägeli in Kützing ex Bornet et Flahault 1887. Ann. Sci. Nat. Bot., ser. 7, 5: 54.',32,NULL,NULL,'Genus','[216]','[53][120]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:17:07','admin'),(200,'Hassallia','Berkeley ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 5: 115.',40,NULL,NULL,'Genus','[217]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(201,'Herpyzonema','Weber van Bosse, 1913. Siboga Exped., p. 36.',39,NULL,NULL,'Genus','[218]','[68]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(202,'Heterocyanococcus','Kufferath, 1929. Ann. Cryptog. Exot. 2: 50.',27,NULL,NULL,'Genus','[219]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-20 06:08:06','admin'),(203,'Heteroleibleinia','(Geitler) Hoffmann, 1985. Cryptog. Algol. 6. 2: 76.',60,'','','Genus','[220]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(204,'Homoeoptyche','Skuja, 1944. Acta Horti Bot. Univ. Riga 14: 53.',38,NULL,NULL,'Genus','[224]','[177]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(205,'Homoeothrix','(Thuret ex Bornet et Flahault) Kirchner 1898, nom. cons. In Engler et Prantl, Nat.Pflanzenfam. 1(1a): 87.',48,NULL,NULL,'Genus','[223]','[8][20][101][109]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(206,'Hormathonema','Ercegović, 1929. Arch. Protistenk. 66: 167. [nomen conservandum]',53,NULL,'The genus <i>Hormathonema</i> was originally described with only one (type) species<i> H. paulocellulare</i><br> Ercegović 1929 (later corrected with slightly modified descriptions; Ercegović 1930, 1932). However, this first species corresponds to the previously described genus <i>Solentia</i> Ercegović 1927 (endolithic, with baeocytic reproduction), and the generic name <i>Hormathonema</i> was later commonly used for another type of mostly epilithic cyanoprokaryotes, from which <i>H. violaceo- nigrum</i> and <i>H. luteo-brunneum</i> are the most characteristic members. The, species <i>H. paulocellulare</i> was transferred therefore into the g. <i>Solentia</i> by Le Campion-Alsumard &amp; Golubić (1985b) and Le Campion-Alsumard &amp; al. (1996) (see p. 457), and the generic name <i>Hormathonema</i> was proposed for conservation in the later sense, with the type species H. violaceo-nigrum. (Komárek & Anagnostidis, 1998)','Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(207,'Hormoscilla','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 425.',47,NULL,NULL,'Genus','[225]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(208,'Hormothamnion','Grunow ex Bornet et Flahault, 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 259.',34,NULL,NULL,'Genus','[226]','[10]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(209,'Hormothece','Jao, 1944. Sinensia 15: 77.',16,NULL,NULL,'Genus','[227]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(210,'Hydrococcus','Kützing, 1833, nom. cons. Linnaea 8: 380. [nomen conservandum]',53,NULL,NULL,'Genus','[228]','[22][132]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-04-11 20:06:39',NULL),(211,'Hydrocoleum','Kützing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 15: 332.',49,NULL,NULL,'Genus','[229]','[3]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(212,'Hydrocoryne','Schwabe ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 5:128.',34,NULL,NULL,'Genus','[230]','[55][86][90]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(213,'Hyella','Bornet et Flahault 1886. J. Bot. 2: 163.',54,'','','Genus','[231]','','','',NULL,NULL,0,1,NULL,0,'active','2019-06-11 06:30:54','admin'),(214,'Hyphomorpha','Borzi, 1916. N. Giorn. Bot. Ital., ser. 2, 23: 582.',26,NULL,NULL,'Genus','[232]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(215,'Isactis','Thuret ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 4: 341.',36,NULL,NULL,'Genus',NULL,'[100]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(216,'Isocystis','Borzì ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 261.',34,NULL,NULL,'Genus','[233]','[142]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-12 04:14:21','admin'),(217,'Iyengariella','Desikachary 1953. Phytomorph. 3(3): 252.',39,NULL,NULL,'Genus','[234]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(218,'Jaaginema','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 395.',64,NULL,NULL,'Genus','[235]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(219,'Johannesbaptistia','De Toni, 1934. Noter. Nomencl. Algol. 1: 6.',18,NULL,NULL,'Genus','[236]','[54][85]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(220,'Katagnymene','Lemmermann, 1899. Abh. Naturwiss. Ver. Bremen 16: 354.',47,NULL,NULL,'Genus','[237]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(221,'Komvophoron','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 372.',47,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(222,'Kyrtuthrix','Ercegović 1929. Arch. Protistenk. 66 (1): 170',36,'','','Genus','[238]','','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(223,'Leibleinia','(Gomont) L. Hoffmann, 1985. Cryptog. Algol. 6, 2: 77.',64,NULL,NULL,'Genus','[239]','[106]',NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(224,'Lemmermanniella','Geitler, 1942. In Engler et Prantl, Nat. Pflanzenfam., ed. 2, 1b: 62.',66,NULL,NULL,'Genus','[240]','[107]',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-12 04:35:54','admin'),(225,'Leptolyngbya','Anagnostidis et Komárek 1988. Algological Studies 50-53: 390.',61,'','','Genus','[241]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(226,'Leptopogon','Borzi, 1906. Nuova Notarisia 18: 38.',32,NULL,NULL,'Genus','[242]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(227,'Letestuinema','Frémy, 1930. Arch. Bot. 3: 390.',26,NULL,NULL,'Genus','[243]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(228,'Limnococcus','(Komárek et Anagnostidis) Komárková, Jezberová, O. Komárek et Zapomělová, 2010. Hydrobiologia 639: 79',18,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:24:47','admin'),(229,'Limnothrix','Meffert, 1988. Arch. Hydrobiol./Algolog. Stud. 50-53: 317.',64,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(230,'Lithococcus','Ercegović, 1925. Acta Bot. Inst. Bot. Zagreb. 1: 83.',16,NULL,NULL,'Genus','[245]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-12 04:59:48','admin'),(231,'Lithomyxa','Howe, 1932. Shorter Contr. Gen. Geol., p. 63.',66,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(232,'Loefgrenia','Gomont 1896. Bot. Notiser 1897: 90.',32,NULL,NULL,'Genus','[246]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:13:05','admin'),(233,'Loriella','Borzì 1892. Nuova Notarisia 1892: 44.',32,NULL,NULL,'Genus','[247]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:14:18','admin'),(234,'Lyngbya','C. Agardh ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 118.',50,NULL,NULL,'Genus','[248]','[117][153][169][171]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(235,'Lyngbyopsis','Gardner, 1927. Mem. New York Bot. Gard. 7: 54.',49,NULL,NULL,'Genus','[249]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(236,'Macrospermum','Komárek, 2008. Fottea 8(1): 81',34,'[29]','','Genus','[250]','','','',NULL,NULL,0,1,'',0,'active','2022-10-11 07:29:56','admin'),(237,'Mantellum','Dangeard, 1941. Botaniste 30: 129.',62,NULL,NULL,'Genus','[252]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(238,'Mastigocladopsis','Iyengar et Desikachary, 1946. Proc. Ind. Acad. Sci. 24B: 158.',39,NULL,NULL,'Genus','[253]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(239,'Mastigocladus','Cohn ex Kirchner 1898. In Engler et Prantl, Nat. Pflanzenfam. 1(1a): 81.',32,NULL,NULL,'Genus','[254]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:16:50','admin'),(240,'Mastigocoleopsis','Geitler 1925. Beih. Bot. Centralbl. 41(2): 258.',32,NULL,NULL,'Genus','[255]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:14:23','admin'),(241,'Mastigocoleus','Lagerheim ex Bornet et Flahault 1887. Ann. Sci. Nat. Bot., ser. 7, 5: 54.',32,NULL,NULL,'Genus','[256]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:19:27','admin'),(242,'Matteia','Borzì 1907. Nuova Notarisia 18: 38.',32,NULL,NULL,'Genus','[257]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:14:29','admin'),(243,'Merismopedia','Meyen, 1839. N. Syst. Pflanzen-Physiol. 3: 440.',62,NULL,'Small-celled Merismopedia species with reddish cell content can be easily misidentified as Thiopedia (Rhodobacteria). - Palinska &amp; al. (1996) isolated from a salinic microbial mats in Norderney Island (Germany) five strains, which corresponded morphologically to three species, M. elegans, M. glauca and M. punctata. They proved the evolutionary relationship to Synechocystis (one strain) and the genotype similarity of all other studied strains by the 16S rDNA sequencing. The stability of different phenotypes, ecotypes, and variability of various species need the further study and confirmation. The identity<br> of, e.g., very variable M. glauca from saline biotopes (sensu Palinska &amp; al. 1996) and M. glauca from acidic peaty waters should be also revised. (Komárek & Anagnostidis, 1998)','Genus','[258]','[4][80]',NULL,NULL,NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(244,'Microchaete','Thuret ex Bornet et Flahault 1887, nom. cons. Ann. Sci. Nat. Bot., ser. 7, 5: 83.[ MICROCHAETE Thuret, Essai de classification des Nostochinees, p.7, 1875 ( Ann. des sc. nat., 6e serie, Bot., I, p. 378).',33,NULL,NULL,'Genus','[259]','[46][73]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(245,'Microcoleus','Desmaziéres ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 15: 350.',49,'[334]','','Genus','[260]','[21][183]','','',NULL,NULL,0,1,'',0,'active','2020-03-24 14:27:23','admin'),(246,'Microcrocis','Richter, 1892. In Hauck et richter, Phyk. Univers., Fasc. 11: 548.',2287,NULL,NULL,'Genus','[261]','[24][87][141]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:23:52','admin'),(247,'Microcystis','Kützing 1833 ex Lemmermann Cryptogamenfl. Mark Brandenb. 3/1: 45, 1907',21,NULL,NULL,'Genus','[262]','[30][39][62][138][166]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(248,'Mojavia','Řeháková et Johansen 2007. Phycologia 46 (5): 488',34,'[50]','','Genus','[264]','','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(249,'Myxobaktron','Schmidle, 1904. Hedwigia 43: 415.',15,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(250,'Myxohyella','Geitler, 1925. Beih. Bot. Centralbl. 41(2): 246.',53,NULL,NULL,'Genus','[265]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(251,'Myxosarcina','Printz, 1921. Kong. Norske Vidensk. Selsk. Skr. 1920(1): 35.',55,NULL,'The genera Chroococcidiopsis and Myxosarcina are distinguishable only by motility of baeocytes according to Waterbury &amp; Stanier (1978). This feature is, however, problematic; the traditional characters distinguish well both these taxa on the generic level. (Komárek & Anagnostidis, 1998)','Genus','[266]','[70]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(252,'Nematoplaca','Geitler, 1933. Arch. Hydrobiol., Suppl. 12: 628.',26,NULL,NULL,'Genus','[267]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(253,'Nephrococcus','Li, 1984. Acta Phytotax. Sin. 22: 191.',16,NULL,NULL,'Genus','[268]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(254,'Nodularia','(Mertens in Jürgens) ex Bornet et Flahault 1888, nom. cons. Ann. Sci. Nat. Bot., ser. 7, 7: 243.',25,NULL,NULL,'Genus','[269]','[158]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-07-16 08:22:42','admin'),(255,'Nostoc','Vaucher ex Bornet et Flahault, 1888. Ann. Sci. Nat. Bot., ser. VII, 7: 181.',34,'','','Genus','[270]','[7][67][89][112][113][125][128][131][137][163][174][182]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(256,'Nostochopsis','Wood ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 5: 80. [NOSTOCHOPSIS Wood, Podromus of a Study of the freshwater Algae of eastern North-Amaerica (Proceeding of the American Philosophical Society held to Philadelphia, p. 126, 1869).',32,NULL,NULL,'Genus','[271]','[123][127]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:19:43','admin'),(257,'Onkonema','Geitler, 1933. Arch. Hydrobiol., Suppl. 12: 627.',53,NULL,NULL,'Genus','[272]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(258,'Oscillatoria','Vaucher ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 198.',50,'','','Genus','[273]','[136][180]','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(259,'Palikiella','Claus 1962. Hydrobiologia 19(2): 201.',64,'','','Genus','[274]','','','',NULL,NULL,0,0,'',0,'active','2020-05-14 12:12:25','admin'),(260,'Pannus','Hickel, 1991. Algolog. Stud. 64: 100.',62,NULL,NULL,'Genus','[275]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(261,'Paracapsa','Naumann, 1924. Ark. Bot. 18: 6.',19,NULL,NULL,'Genus','[276]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(262,'Parenchymorpha','Tseng et Hua 1984. Sci. Sin., ser. B. 27(8): 813.',39,NULL,NULL,'Genus','[277]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(263,'Parthasarathiella','Subba Raju 1962. Trans. Amer. Microscop. Soc. 81: 93.',9,NULL,NULL,'Genus','[278]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-12 11:18:31','admin'),(264,'Pascherinema','de Toni, 1936. Noter. Nomencl. Algol. 8: 5.',58,NULL,NULL,'Genus','[279]','[69]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:46:21','admin'),(265,'Petalonema','Berkeley ex Correns, 1889. Flora 72: 321.',37,NULL,NULL,'Genus','[280]','[18][47]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(266,'Phormidiochaete','Komárek in Anagnostidis, 2001. Preslia, Praha, 73(4):374-375',48,NULL,NULL,'Genus','[282]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(267,'Phormidium','Kützing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 156.',50,NULL,NULL,'Genus','[283]','[38][94]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 07:25:27','admin'),(268,'Cyanoplacoma','(Schousboe ex Bornet et Thuret) Molinari et Guiry 2021. Notulae Algarum 183: 2',19,'[621]','','Genus','[284]','[1045]',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2022-08-11 13:50:51','admin'),(269,'Planktocyanocapsa','Hindák, 2002. Biológia, Bratislava, 57(4): 418',21,NULL,NULL,'Genus','[221][222]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(270,'Planktolyngbya','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 394.',64,NULL,NULL,'Genus','[285]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-06-12 12:15:43','admin'),(271,'Planktothricoides','Suda et M. M. Watanabe in Suda et al. 2002, Int. J. of Syst. and Evol. Microbiol 52: 1593',49,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(272,'Planktothrix','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 414.',49,NULL,NULL,'Genus','[286]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(273,'Plectonema','Thuret ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 96.',50,NULL,NULL,'Genus','[287]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(274,'Pleurocapsa','Thuret in Hauck, 1885. Rabenhorst´s Kryptogamenfl., ed. 2, 2: 515.',2557,'[349][350]','','Genus','[288]','[49][126][151]','','',NULL,NULL,0,1,'',0,'active','2023-02-01 09:28:54','admin'),(275,'Podocapsa','Ercegović, 1931. Acta Bot. Inst. Bot. Univ. Zagreb. 6: 33.',54,NULL,NULL,'Genus','[289]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(276,'Polychlamydum','West et West, 1897. J. Bot. 35: 271.',50,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(277,'Porphyrosiphon','Kützing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 15: 331.',49,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(278,'Prochlorococcus','Chisholm, Frankel, Goericke, Olson, Palenik, Waterbury, West-Johnsrud et Zettler in Komárek et al. 2020. Fottea 20(2): 178',416,'[93][574]','','Genus','[293]','','','',NULL,NULL,0,1,NULL,0,'active','2021-05-27 13:39:01','admin'),(279,'Prochloron','Lewin, 1977. Phycologia 16(2): 217',63,NULL,NULL,'Genus','[290][292]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(280,'Prochlorothrix','Burger-Wiersma, Stall et Mur 1989',2532,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 11:57:49','admin'),(281,'Proterendothrix','W. et G.S. West, 1897. J. Bot. 35: 299.',42,NULL,NULL,'Genus','[294]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(282,'Pseudanabaena','Lauterborn, 1915. Verh. Naturhist.-Med. Vereins Heidelberg, ser. 2, 13: 437.',64,NULL,'17 species in three subgenera:<br>Pseudanabaena, Skujanema Anagnostidis et Komárek 1988, and Ilyonema Anagnostidis et Komárek 1988.','Genus','[295]','[9]',NULL,NULL,NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(283,'Pseudocapsa','Ercegović, 1925. Acta Bot. Inst. Univ. Zagreb. 1: 95.',16,NULL,NULL,'Genus','[296]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(284,'Pseudoncobyrsa','Geitler, 1925. Beih. Bot. Centralbl. 41 (2): 237.',16,NULL,NULL,'Genus','[297]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(285,'Pseudophormidium','(Forti) Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 409.',61,NULL,NULL,'Genus','[298]','[77]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:33:12','admin'),(286,'Pseudoscytonema','Elenkin, 1949. Monogr. Algarum Cyanophyc., Pars Spec. 2: 1805.',49,NULL,NULL,'Genus','[299]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(287,'Pulvinularia','Borzi, 1916. Nuovo Giorn. Bot. Ital., ser. 2, 23: 574.',38,NULL,NULL,'Genus','[300]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(288,'Radaisia','Sauvageau, 1895. J. Bot. 9: 374.',54,NULL,NULL,'Genus','[301]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(289,'Radiocystis','Skuja 1948, Symb. Bot. Uppsala 9(3): 43.',16,NULL,NULL,'Genus','[302]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-25 10:39:33','admin'),(290,'Raphidiopsis','Fritsch et Rich, 1929. Trans. Roy. Soc. South Africa 18: 91.',25,NULL,NULL,'Genus','[303]','null[557]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-10-11 07:40:39','admin'),(291,'Rexia','Casamatta, Gomez et Johansen 2006. Hydrobiologia 561: 23',40,NULL,NULL,'Genus','[304]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(292,'Rhabdoderma','Schmidle et Lauterborn, 1900. Ber. Deutsch. Bot. Ges. 18: 148.',66,NULL,NULL,'Genus','[305]','[33][167]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(293,'Rhabdogloea','Schröder, 1917. Ber. Deutsch. Bot. Ges. 35: 549.',66,NULL,NULL,'Genus','[306]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(294,'Rhodostichus','Geitler et Pascher in Geitler, 1931. Arch. Protistenk. 73: 310.',66,NULL,NULL,'Genus','[307]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(295,'Richelia','J. Schmidt in Ostenfeld et J. Schmidt 1901. Vidensk. Meddel. Dansk Naturhist.Foren. København, p. 146.',34,NULL,NULL,'Genus','[309]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(296,'Rivularia','[Roth] C. Agardh ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 4: 345; (pre-starting-point syn.).',36,NULL,NULL,'Genus',NULL,'[5][56][64][76][84][186]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(297,'Romeria','Koczwara in Geitler, 1932. Rabenhorst´s Kryptogamenfl. Deutschl., ed. 2, 14: 915.',65,'[27]','The genus was described (generic diagnosis) as <em>Raciborskia</em>; the valid name <em>Romeria </em> was established as nomenclatoric change','Genus','[310][311][312][313][322][315]','[6][32][144]','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(298,'Rubidibacter','Choi, Noh, Lee et Rho 2008. Int. J. of Systematic and Evolutionary Microbiology 58: 2811',2558,'[47]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:33:05','admin'),(299,'Sacconema','Borzi ex Bornet et Flahault, 1886. Ann. Sci. Nat. Bot., ser. 7, 3: 381.',36,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(300,'Schizothrix','Kützing ex Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 292',430,'[145]','','Genus','[327]','[59][93][94][96][99][148]','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(301,'Schmidleinema','De Toni, 1936. Noter. Nomencl. Alg. 8: 5.',32,NULL,NULL,'Genus','[328]','[31]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(302,'Scytonema','Agardh ex Bornet et Flahault 1887. Ann. Sci. Nat. Bot., ser. 7, 5: 85.',37,NULL,NULL,'Genus','[329]','[60][61][66][78][98][175]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(303,'Scytonematopsis','Kiseleva 1930. Zhurn. Russk. Bot. Obsc. 15: 174.',37,NULL,NULL,'Genus','[330]','[152][179]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-13 08:32:56','admin'),(304,'Seguenzaea','Borzì 1907. Atti Congr. Nat. Ital. Milano 1906: 372.',40,NULL,NULL,'Genus','[331]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(305,'Sinaiella','Gruia 1965. Revista Biol. 5: 167.',42,NULL,NULL,'Genus','[332]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-13 08:36:55','admin'),(306,'Siphononema','Geitler, 1925. Arch. Protistenk. 51: 332.',19,NULL,NULL,'Genus','[333]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(307,'Siphonosphaera','Hindák, 1988. Algolog. Stud. 49: 416.',71,NULL,NULL,'Genus','[334]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(308,'Sirocoleum','Kützing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 15: 347.',49,NULL,NULL,'Genus','[335]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(309,'Snowella','Elenkin, 1938. Monogr. Algarum Cyanophyc., Pars Spec., 1: 278.',71,NULL,NULL,'Genus','[336]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(310,'Sokolovia','Elenkin, 1926. Bot. Mater. Inst. Sporov. Rast. Glavn. Bot. Sada RSFSR 4: 90.',61,NULL,NULL,'Genus','[337]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:34:32','admin'),(311,'Solentia','Ercegović, 1927. Acta Bot. Inst. Bot. Univ. Zagreb. 2: 79.',54,NULL,'According to the revision of LeCampion-Alsumard &amp; al.(1996), the genus Solentia is euendolithic, characterized by the mainly endolithic, wide gelatinous stalks, in which the few cells are situated at the ends or sparsely along the stalk, distant one far from another. Reproduction by baeocyte formation. (Komárek & Anagnostidis, 1998)','Genus','[338]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(312,'Spelaeopogon','Borzi, 1907. Nuova Notarisia 18: 38.',32,NULL,NULL,'Genus',NULL,'[143]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(313,'Sphaerocavum','Azevedo et Sant\' Anna, 2003. Arch. Hydrobiol./ Algological Studies 109: 81',21,'','','Genus','[339]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-06-18 08:45:39','admin'),(314,'Sphaerospermopsis','Zapomělová, Jezberová, Hrouzek, Hisem, Řeháková et Komárková, 2010. Journal of Phycology 46: 415.',25,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-10-06 06:22:45','admin'),(315,'Spirirestis','Flechtner et Johansen in Flechtner et al., 2002, Nova Hedwigia 74(1-2): 6&nbsp;',40,'[201]','','Genus','[340][341]','','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(316,'Spirulina','Turpin ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 249.',56,NULL,NULL,'Genus','[342]','[82][168][172]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(317,'Stanieria','Komárek et Anagnostidis, 1986. Algolog. Stud. 38-39: 208.',2557,NULL,NULL,'Genus','[343]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:30:23','admin'),(318,'Starria','Lang, 1977. J. Phycol. 13: 289.',47,NULL,NULL,'Genus','[344]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(319,'Stauromatonema','Frémy, 1930. Arch. Bot. 3: 385.',26,NULL,NULL,'Genus','[345]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(320,'Stichosiphon','Geitler, 1932. Rabenhorst´s Kryptogamenfl. Deutschl., ed. 2, 14: 411.',58,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:47:07','admin'),(321,'Stigonema','Agardh ex Bornet et Flahault, 1888. Ann. Sci. Nat. Bot., ser. 7, 5: 62.',38,NULL,NULL,'Genus','[346]','[154]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(322,'Symphyonema','Jao, 1944. Sinensia 15: 81.',39,'[450]','','Genus','[347]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-10-08 04:52:53','admin'),(323,'Symphyonemopsis','Tiwari et Mitra, 1969. Phykos 7: 193.',39,NULL,NULL,'Genus','[348]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(324,'Symploca','Kützing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 104.',49,NULL,NULL,'Genus','[349]','[51][130][176]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(325,'Symplocastrum','(Gomont) Kirchner, 1898. In: Engler et Prantl, Nat. Pflanzenfam. 1(1a): 69.',49,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(326,'Synechococcus','Nägeli, 1849. Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss.(Gatt. einzell. Algen) 10(7): 56.',66,'','Synechococcus is important experimental model organism the strains of which grow well in different types of culture equipments. To this genus belong also different strains designated commonly as Anacystis nidulans and ˝Agmenellum quadruplicatum˝ (=<em>Synechococcus nidulans</em>). The solitary Synechococcus cells without mucilage grow well in homogeneous liquid solutions.&nbsp;','Genus','[350]','[12][37][103]',NULL,NULL,NULL,NULL,1,1,NULL,0,'active','2021-05-28 06:46:47','admin'),(327,'Synechocystis','Sauvageau 1892. Bull. Soc. Bot. Fr. 39: 115.',62,NULL,NULL,'Genus','[351]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-13 10:52:36','admin'),(328,'Tapinothrix','Sauvageau, 1893. Bull. Soc. Bot. Fr. 39(1892): 123.',61,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:34:24','admin'),(329,'Thalpophila','Borzì 1907. Atti Congr. Nat. Ital. 1906: 373.',32,NULL,NULL,'Genus','[352]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:16:58','admin'),(330,'Thermosynechococcus','Katoh, Itoh, Shen et Ikeuchi in Komárek et al. 2020. Fottea 20(2): 184',2334,'[574]','','Genus','[354][353]','','','',NULL,NULL,0,1,NULL,0,'active','2021-05-28 06:42:55','admin'),(331,'Thiochaete','Welsh 1961. Nova Hedwigia 3: 39.',34,NULL,NULL,'Genus','[355]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-13 10:55:14','admin'),(332,'Tolypothrix','Kützing ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 5: 118.',40,NULL,NULL,'Genus','[356]','[150]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(333,'Trichocoleus','Anagnostidis, 2001. Preslia, Praha, 73: 369',1068,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(334,'Trichodesmium','Ehrenberg ex Gomont, 1892, nom. cons. Ann. Sci. Nat. Bot., ser. 7, 16: 193.',49,NULL,NULL,'Genus','[357]','[81][83][133][155][185]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(335,'Trichormus','(Ralfs ex Bornet et Flahault) Komárek et Anagnostidis 1989. Algolog. Stud. 56: 303.',34,NULL,NULL,'Genus','[358]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(336,'Tryponema','Ercegović, 1929. Arch. Protistenk. 66: 168.',19,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(337,'Tubiella','Hollerbach, 1935. Acta Inst. Bot. Acad. Sci. SSSR, ser. 2, 2: 34.',65,NULL,NULL,'Genus','[359]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(338,'Tychonema','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 410.',49,NULL,NULL,'Genus','[360]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(339,'Umezakia','M. Watanabe, 1987. Bull. Nat. Sci. Mus., ser. B, 13(3): 81.',25,NULL,NULL,'Genus','[361]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:16:05','admin'),(340,'Voukiella','Ercegović, 1925. Acta Bot. Inst. Bot. Univ. Zagreb. 1: 92.',39,NULL,NULL,'Genus','[362]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(341,'Westiella','Borzì 1907. Atti Congr. Nat. Ital. 1906: 373.',32,NULL,NULL,'Genus','[363]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:15:51','admin'),(342,'Westiellopsis','Janet, 1941. Ann. Bot. London, ser. 2, 5: 170.',32,NULL,NULL,'Genus','[364]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(343,'Wilmottia','Strumecký, Elster et Komárek, 2011. Fottea 11(1): 62',2555,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:34:49','admin'),(344,'Wollea','Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 223.',34,NULL,NULL,'Genus','[365]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(345,'Wolskyella','Claus, 1963. Nova Hedwigia 6: 32.',65,NULL,NULL,'Genus','[366]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(346,'Woronichinia','Elenkin, 1933. Trudy Bot. Inst. Akad. Nauk SSSR, ser. 2, Sporov. Rast. 1: 28.',71,NULL,NULL,'Genus','[367]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(347,'Xenococcus','Thuret in Bornet et Thuret, 1880. Notes Algol. 2: 74.',55,NULL,'About 20 described species, the majority of which need revision.','Genus','[368]','[45]',NULL,NULL,NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(348,'Xenotholos','Gold-Morgan, Montejano et Komárek, 1994. Arch. Protistenk.144: 391.',55,NULL,NULL,'Genus','[369]',NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(349,'Yonedaella','Umezaki 1962. Taxon 11 60: 204.',47,'','','Genus','','','','',NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:44:33','admin'),(350,'Amphithrix','Bornet et Flahault, 1886',36,NULL,NULL,'Genus',NULL,'[101]',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2019-06-14 05:32:20','admin'),(351,'Physactis','Küzing 1843',36,NULL,'A type species (generitype) appears not to have been designated - taxonomic status is uncertain, requiring further investigation','Genus',NULL,'[134]',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2019-06-12 12:07:01','admin'),(353,'Democladicidae','Gloch ex Glgúň, 1848',1,'','','Subclass',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(355,'Democladales','Glgúň et Smeagol, 1836',353,'','','Order',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(356,'Exemplocladales','Unknown author',353,'','','Order',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(357,'Mysterioordus','Žáříneček, Řáňušová et Šůžele, 2015',356,'[10][12][53][57][26][30][20][9][27][32][55][28][33][46][34][40]','','Genus',NULL,'[3][4][5][6][7][8][9][10][11][12][17][19][18][20][21][22][23][24][25][26][27][28][29][30][31][32][33][38][39][40][41][42][44][43][45][46][47][48]',NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(358,'Exemplocladaceae','Wo et Tso, Tujde Mag. 16:29, 1995',356,'','','Family',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(359,'Exemplophyceae','K.Ontrovéz, Las Páginas sobre las cosas mínusculas, 1982',356,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(360,'Democladus','Linné et Oleum, 1778',1,'','Demo note for a demo clade. Containing <strong>bold</strong> and <em>italic</em> text!','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(361,'Pseudocladoidella','Linné et Cukrowicz, 1768',358,'','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(362,'Pseudocladoidella Group A','Linné et Cukrowicz, 1769',361,NULL,NULL,'Species group',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(363,'Pseudocladoidella formerly ″Parapseudocladoideodelia″','Cukrowicz et Kolomotovova, Viergaldiche Gestaftsmacheningen und Vorlaage, 1775',361,'','','Species group',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(364,'Democladus demonstrativus','Ya, Sam et Nigdoinni, <em>2002</em>',360,NULL,'Used to be spelled \'<em>daemonstrativus</em>\',<br>but it was later changed in the \'<span style=\'font-family: Verdana,Geneva,sans-serif; font-size: 14px;\'><strong>LARGE-LETTERED JOURNAL</strong></span>\'<br><span style=\'font-size: 10px;\'>(see <a href=\'https://google.com\' target=\'_blank\' rel=\'noopener noreferrer\'>Google</a>)</span>','Species',NULL,NULL,NULL,NULL,NULL,NULL,1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(365,'Pseudocladoidella sibogiensis','Anna Weber-van Bosse 1900',363,NULL,'The Dutch phycologist Anna Antoinette Weber-van Bosse (1852- 1942) certainly demonstrated the spirit of adventure that qualifies her to be counted in the ranks of \'phycological trailblazers.\'Unfortunatelly, she did never discover <em>Pseudocladoidella sibogiensis,</em> and thus this species remains solely a fruit of our imagination.','Species',NULL,NULL,NULL,NULL,NULL,NULL,1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(366,'Democladus secundus','<br>',360,'[10][12]',NULL,'Species group',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(367,'Coleodesmium wrangelii','Borzì ex Geitler 1942',137,'','','Species',NULL,'',NULL,NULL,NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(368,'Squeltestivus','M.Y. Squel, 2017',1,'','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(369,'Lastidinsertysticidae','PDO',1,'','','Family',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(370,'Lastidinsertystis','Hob et It, 2017',1,'','','Genus',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(371,'Lastidinsertystis testivus','Hob et It, 2017',1,'','','Species',NULL,'','','',NULL,NULL,1,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(372,'Lastidinsertystis correctivus','Hob et It, 2017',1,'','','Species group',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(373,'Lastidinsertystis correctivus finalissimus','Hob et It, 2017',1,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(374,'Lastidinsertystis evenbeteris','Hob et It, 2017',1,'','','Species','[415][412]','','ATTIQ-HRB','XS120-b','Lava Pools','[86][65][168][38][166][1][185][186][187][188][189][190]',0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(375,'Lastidinsertysticidaceae clade A','',1,'','','Subfamily/Tribe',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(383,'Pseudocladoidella parapseudocladoideodelioides','',363,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(384,'Halomicronema excentricum','Abed, Garcia-Pichel &amp; Hernández-Mariné 2002. Archives for Microbiology 177: 369',196,'[69]','does not meet ICN/ICNP requirements for holotype/type strain','Species',NULL,'','','TFEP1','microbial mat','',1,0,'',0,'active','2019-06-13 09:06:04','admin'),(385,'Halomicronema hongdechloris','Chen, Li, Birch &amp; Willows 2012. FEBS Letters 586',196,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(386,'Brasilonema octagenarum','Aguiar, Fiore, Franco, Ventrella, Lorenzi, Venetti et Alfenas, 2008, J. Phycol. &nbsp;44(5): 1325',118,'[71]','','Species',NULL,'','BRNM/HY 1416','UFV-E1','Epiphytic','[169]',0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(387,'Hassallia bysssoidea','Hassall ex Bornet et Flahault',200,'[73]','','Species',NULL,'','K','CCALA 823',NULL,NULL,1,1,NULL,0,'active','2019-10-04 05:13:16','admin'),(388,'Rexia erecta','Casamatta, Gomez et Johansen 2006. Hydrobiologia 561: 23',291,'[15]','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(389,'Roholtiella','Bohunická, Pietrasiak et Johansen 2015. Phytotaxa 197(2): 88',34,'[74]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 10:41:45','admin'),(390,'Roholtiella edaphica','Bohunická et Lukešová 2015. Phytotaxa 197(2): 89',389,'[74]','','Species',NULL,'','CBFS A-041-1','CCALA 1063','soil','[113]',1,1,NULL,0,'active','2021-06-18 09:17:17','admin'),(391,'Roholtiella bashkiriorum','Gaysina et Bohunická 2015. Phytotaxa 197(2): 90',389,'[74]','','Species',NULL,'','CBFS A-036-1','CCALA 1057','soil','[117]',0,1,NULL,0,'active','2021-06-18 09:15:54','admin'),(392,'Roholtiella fluviatilis','Johansen et Gaysina 2015. Phytotaxa 197(2): 92',389,'[74]','','Species',NULL,'','CBFS A-038-1','CCALA 1058','water’s edge of the stream','[117]',0,1,NULL,0,'active','2021-06-18 09:17:40','admin'),(393,'Roholtiella mojaviensis','Pietrasiak et Johansen 2015. Phytotaxa 197(2): 92',389,'[74]','','Species',NULL,'','CBFS A-039-1','CCALA 1051','desert soil','',0,1,NULL,0,'active','2019-07-25 10:44:24','admin'),(394,'Anathece','Komárek et al., 2011. Europ. J. Phycol. 46(3): 321.',416,'[75]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:29:20','admin'),(395,'Cyanocatena','Hindák, 1975. Algolog. Stud. 13: 334.',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(396,'Cyanocatenula','Joosten, 2006. Flora of the blue-green algae of the Netherlands I., p. 34.',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(397,'Cyanogranis','Hindák, 1982. Algolog. Stud. 32: 244-245.',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(398,'Cyanonephron','Hickel, 1985. Algolog. Stud. 38/39: 100.',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(399,'Epigloeosphaera','Komárková-Legnerová, 1991. Algolog. Stud. 62: 10-11',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(400,'Gloeomargarita','Moreira, Tavera, Benzerara, Skouri-Panet, Couradeau, Gérard, Fonta, Novelo, Zivanovic et López-García 2017. International Journal of Systematic and Evolutionary Microbiology 67: 657',2529,'[81]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:39:30','admin'),(401,'Lemmermanniella','Geitler, 1942',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'active','2019-06-12 04:34:22','admin'),(402,'Lithococcus','Ercegovic 1925. Acta Bot. Univ. Zagreb 1: 83',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-06-12 04:59:31','admin'),(403,'Lithomyxa','Howe, 1932. Prof. Papers, United State Geological Survey, 170: 57-64',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(404,'Neosynechococcus','Dvořák, Hindák, Hašler et Hindáková 2014. Phytotaxa 170(1): 26',2549,'[85]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:37:34','admin'),(405,'Aphanocapsa','Nägeli, 1849. Neue Denks. Allg. Schweiz. Ges. Ges. Naturw. 10(7): 52',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(406,'Coccopedia','Troickaja, 1922. Bot. Mater. Inst. Spor. Rast. Glav. Bot. Sada RSFSR, 1: 129-131',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(407,'Cyanotetras','Hindák, 1988. Preslia 60: 289-308',62,'[87]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(408,'Eucapsis','Clements et Shantz. 1909.<em>&nbsp;</em>Minnesota Bot. Stud. 4: &nbsp;134',62,'[88]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(409,'Limnococcus','Komárková et al., 2010. Hydrobiologia 639: 79',62,'[38]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(410,'Mantellum','Dangeard, 1941. Le Botaniste 30: &nbsp;129-131',62,'[89]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(411,'Merismopedia','Meyen, 1839. Neues system der pflanzen-physiologie, 1-627',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(412,'Microcrocis','Richter, 1882.',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(413,'Pannus','Hickel, 1991. Algolog. Stud. 64: &nbsp;100-101',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(414,'Synechocystis','Sauvageau, 1892. Bull. Soc. Bot. Fr. 39: 104-128',62,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(415,'Prochlorococcales','',1,'','','Order',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(416,'Prochlorococcaceae','Komárek et Strunecký 2020. Fottea 20(2):178',13,'[574]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2021-05-27 13:36:21','admin'),(417,'Cyanobium','Rippka et Cohen-Bazire, 1983. Annal. Inst. Pasteur, Microbiol. 134B: &nbsp;21-36.',66,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(418,'Parasynechococcus','Coutinho, Tschoeke, Thompson et Thompson in Komárek et al. 2020. Fottea 20(2)182',416,'[574]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2021-05-27 13:46:45','admin'),(419,'Prochlorococcus','Chisholm et al., 1992. Arch. Microbiol. 157: 297-300',1,'','','Genus',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(420,'Coelomoron','Buell, 1938. Bull. Torrey Bot. Club 65: 377-396',59,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(421,'Coelosphaeriopsis','Lemmermann 1899. A<span itemprop=\'name\'>bhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen 16: 352</span>',59,'[95]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(422,'Coelosphaerium','Nägeli, 1849. Neue Denksch. Allg. Schweiz. Ges. Gesam. Naturwiss. 10(7): &nbsp;54',59,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(423,'Siphonosphaera','Hindák, 1988. Algolog. Stud. 49: 416-417',59,'','','Genus','[334]','','','',NULL,NULL,0,1,NULL,0,'active','2019-06-13 08:40:16',NULL),(424,'Snowella','Elenkin 1938. Monogr. Algarum Cyanophyc., Pars Spec., 1: 278',59,'','','Genus','[336]','','','',NULL,NULL,0,1,NULL,0,'active','2019-06-13 08:44:24','admin'),(425,'Woronichinia','Elenkin, 1933. Trudy Bot. Inst. Akad. Nauk SSSR, Ser. 2, 1: &nbsp;17-21.',59,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(426,'Acaryochloris','Miyashita et Chihara 2003. Journal of Phycology 39: 1249.',57,'[46]','the type species descrition does not meet requiremets of art. 8.4 of the ICN and Rule 27 of the ICNP','Genus',NULL,'','','','Mainly as a symbiont in colonial ascidians','',0,0,'',0,'active','2023-01-27 11:52:06','admin'),(427,'Cyanodictyon','Pascher, 1914. Berich. Deuts. Bot. Ges. 32(5): &nbsp;339-352',66,'','','Genus',NULL,'[160]','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(428,'Pseudanabaenales','Hoffmann, Komárek &amp; Kaštovský, 2005. Algolog. Stud. 117: 95-115',1,'','','Order',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(429,'Romeriaceae','Komárek et al., 2014. Preslia 86: 305',428,'','','Family',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(430,'Schizotrichaceae','Elenkin, 1949.',13,'','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(431,'Cyanocatenula','Joosten, 2006. Flora of the blue-green alga of the Netherlads, p. 207',65,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(432,'Alkalinema','Vaz et al. 2015, IJSEM 65: 302&nbsp;',61,'[100]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(433,'Allysophoron','&nbsp;Anagnostidis et Komárek 1988. Algolog. STud. 50-53: 373 &nbsp;(sub <em>Komvophoron</em>)',64,'','','Genus',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(434,'Arthronema','Komárek et Lukavský, 1988. Algolog. Stud. 50-53: 266',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(435,'Jaaginema','Anagnostidis et Komárek, 1988. Algolog. Stud. 50-53: 395',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(436,'Johanseninema','Hašler et al. 2014, Preslia 86: 293',64,'','','Genus',NULL,'[188]','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(437,'Limnothrix','Meffert 1988, Aloglog. Stud. 50-53: 269-270',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(438,'Onodrimia','Jahodářová, Dvořák et Hašler 2017. Phytotaxa 326(1): 30',61,'[121]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(439,'Onodrimia javanensis','Jahodářová et al.',438,'','','Species',NULL,'','','',NULL,NULL,1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(440,'Pinocchia','Dvořák, Jahodářová et Hašler 2015. Fottea 15(1): 114',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(441,'Pseudanabaena','Lauterborn 1915, <em>Verh. Naturhist.-Mediz. Ver. Heidelberg </em> 13: &nbsp;395-481',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(442,'Pseudoscillatoria','Rasoulouniriana et al. 2009, Diseases Aquat. Org. 87: &nbsp;91-96',49,'[108]','genus not formally designated','Genus',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(443,'Yonedaella','Umezaki 1962, Taxon 10: 204',64,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(444,'Haloleptolyngbya','Dadheech, Mahnoud, Kotut et Krienitz 2012. Hydrobiologia 691: &nbsp;272',416,'[110]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:28:25','admin'),(445,'Kovacikia','Miscoe, Pietrasiak et Johansen 2016. Bibliotheca Phycologica 120: 83',61,'[111]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(446,'Acaryochloridaceae','Komárek et al. 2014',8,'[1]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(447,'Komarekiella','G.S. Hentschke, J.R. Johansen et C.L. Sant’anna 2017. Fottea 17(2): 180',34,'[113]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 10:35:30','admin'),(448,'Komarekiella atlantica','G.S. Hentschke, J.R. Johansen et C.L. Sant Anna',447,'','','Species',NULL,'','SP469725','CCIBt3483','Atlancit rain foresst, wood, concrete','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(449,'Kryptousia','Alvarenga, Andreote, Branco et Fiore',40,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(450,'Kryptousia macronema','Alvarenga, Andreote, Branco et Fiore',449,'[114]','','Species',NULL,'','SP469781','CENA338T','Avicennia leaves','[172]',1,1,NULL,0,'active','2021-06-18 09:31:55','admin'),(451,'Kryptousia microlepis','Alvarenga, Andreote, Branco et Fiore',449,'','','Species',NULL,'','SP469782','CENA354T','Avicennia and Merostachys leaves','[172]',0,1,NULL,0,'active','2021-06-18 09:31:47','admin'),(452,'stichodo','',22,'','','Subfamily/Tribe',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(453,'Aphanothece','Nägeli 1849, nom. cons., Gattungen einzelliger Algen: 59',15,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(454,'Aphanothece microscopica','Nägeli 1849, nom. cons., Gattungen einzelliger Algen: 59',106,'','','Species',NULL,'','iconotype, Nägeli 1849, pl. I., H, fig 1','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(455,'appp','',106,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(456,'Roseofilum','Casmatta, Stanić, Gantar et Richardson 2012. Phycologia 51(5): 494',46,'[116]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:23:29','admin'),(457,'Roseofilum reptotaenium','Casmatta, Stanić, Gantar et Richardson 2012. Phycologia 51(5): 494',456,'[116]','','Species',NULL,'','BRY C-53584','','scleractinian coral host Siderastrea siderea','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(458,'Roseofilum corallyticum','(Rützler &amp; Santavy) Casamatta, Stanić, Gantar et Richardson 2012. Phycologia 51(5): 496',456,'[314]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1117',0,'active','0000-00-00 00:00:00',NULL),(459,'Thermoleptolyngbya','Sciuto et Moro 2016. Molecular Phylogenetics and Evolution 105: 33',1034,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:25:56','admin'),(460,'Thermoleptolyngbya albertanoe','Sciuto et Moro 2016. Molecular Phylogenetics and Evolution 105: 33',459,'','','Species',NULL,'','PAD A000626','CCALA 10257','thermal mud','[69]',1,1,NULL,0,'active','2021-10-07 13:05:08','admin'),(461,'Haloleptolyngbya alcalis','Dadheech, Mahnoud, Kotut et Krienitz 2012. Hydrobiologia 691: &nbsp;273',444,'[110]','','Species',NULL,'','B 400040749','UTEX B ZZ879','Plankton','[207]',1,1,NULL,0,'active','2021-06-18 11:00:36','admin'),(462,'Leptolyngbya corticola','Johansen et Kováčik 2011. Nova Hedwigia 92(3-4): 291',225,'[118]','','Species',NULL,'','BRY 37704','CCALA 085','bark of Fagus sylvatica','[54]',0,1,'',0,'active','2021-06-18 11:10:07','admin'),(463,'Scytolyngbya','Song et Li 2015. Phytotaxa 224(1): 74',61,'[119]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(464,'Scytolyngbya timoleontis','Song et Li 2015. Phytotaxa 224(1): 74',463,'[119]','','Species',NULL,'','CHCB XS 20120601','','epilithically on well’s stones (with dim light) in a water treatment facility with high Fe and Mn contents','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(465,'Aliterellaceae','Rigonato, Gama, Alvarenga, Branco, Brandini, Genuário et Fiore 2016. IJSEM 66: 2859',7,'[120]','','Family',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(466,'Aliterella','Rigonato, Gama, Alvarenga, Branco, Brandini, Genuário et Fiore 2016. IJSEM 66: 2859',23,'[120]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-02-01 13:45:30','admin'),(467,'Aliterella atlantica','Rigonato, Gama, Alvarenga, Branco, Brandini, Genuário et Fiore 2016. IJSEM 66: 2859',466,'[120]','','Species',NULL,'','SP 469035','CENA 595','marine, 107 m depth','',1,1,'',0,'active','2019-06-12 14:33:43','admin'),(468,'Aliterella antarctica','Rigonato, Gama, Alvarenga, Branco, Brandini, Genuário et Fiore 2016. IJSEM 66: 2860',466,'','','Species',NULL,'','SP 469036','CENA 408','ornithogenic soil with decomposing Deschampsia','',0,1,'',0,'active','2019-06-12 14:33:49','admin'),(469,'Onodrimia javanensis','Jahodářová, Dvořák et Hašler 2017. Phytotaxa 326(1): 30',438,'[121]','','Species',NULL,'','OLM 9224','UPOC E28/2016','Submersed bark of tree branches which fell into the hot water spring in rainforest','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(470,'Pinocchia polymorpha','Dvořák, Jahodářová et Hašler 2015. Fottea 15(1): 115',440,'','','Species',NULL,'','OLM Botany 24: 9219','UPOC 62-P/2013','Plankton and periphyton of freshwater tropical lake','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(471,'Oxynema','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012. Cryptogamie, Algologie 33(1):50',49,'[122]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(472,'Oxynema lloydianum','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012. Cryptogamie, Algologie 33(1):56',471,'[122]','','Species',NULL,'[265]','PC 0655991','',NULL,NULL,0,1,'clades:1194',0,'active','0000-00-00 00:00:00',NULL),(473,'Oxynema thaianum','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012. Cryptogamie, Algologie 33(1):50',471,'[122]','','Species',NULL,'','BRNM HY2363','CCALA 960','surface of wet salty soil in saltworks, sometimes in shallow water','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(474,'Oxynema acuminatum','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012. Cryptogamie, Algologie 33(1):56',471,'[122]','','Species',NULL,'[266][627]','PC 0655992','',NULL,NULL,0,1,'clades:1195',0,'active','2019-11-14 12:21:23','admin'),(475,'Kovacikia muscicola','Miscoe, Pietrasiak et Johansen 2016. Bibliotheca Phycologica 123: 80',445,'[111]','','Species',NULL,'','BISH 755073','HA7619-LM3','among mosses growing on the cave walls','',1,1,NULL,0,'active','2019-05-24 05:28:11','admin'),(476,'Cyanosarcina radialis','Miscoe, Pietrasiak et Johansen 2016. Bibliotheca Phycologica 120: 82',159,'[111]','','Species',NULL,'','BISH 755072','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(477,'Aphanocapsa lilacina','Miscoe et Johansen 2016. Bibliotheca Phycologica 120: 82',105,'[111]','','Species',NULL,'','BISH 755071','','basaltic rock walls near cave entrance','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(478,'Oculatella','Zammit, Billi et Albertano 2012. European Journal of Phycology 47(4): 351',1034,'[123]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(479,'Oculatella subterranea','Zammit, Billi et Albertano 2012. European Journal of Phycology 47(4): 352',478,'[123]','','Species',NULL,'','ARG CY21175','VRUC 135/Albertano 1985','&nbsp;biofilms on illuminated limestone in subterranean sites','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(480,'Oculatella kauaiensis','Miscoe et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 460',478,'[111][547]','','Species',NULL,'','BISH 755074','CCALA 1040','Damp cave wall in tropical island biome.','[113]',0,1,'',0,'active','2020-05-27 11:40:48','admin'),(481,'Stenomitos','Miscoe et Johansen 2016. Bibliotheca Phycologica 120: 84',61,'[111]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(482,'Stenomitos rutilans','Miscoe et Johansen 2016. Bibliotheca Phycologica 120: 85',481,'[111]','','Species',NULL,'','BISH 755075','','associated with moss growing on the basaltic cave walls','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(483,'Acaryochloris marina','Miyashita et Chihara 2003. Journal of Phycology 39: 1249',426,'','','Species',NULL,'','','MBIC11017','Mainly as a symbiont in colonial ascidians','',1,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(484,'Spelaeonaias','Lamprinou, Christodoulou, Hernández -Mariné et Economou-Amilli in Lamprinou et al. 2016. Phytotaxa 282(3): 175',37,'[124]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-02-01 13:55:06','admin'),(485,'Spelaeonainas floccida','Lamprinou, Christodoulou, Hernández -Mariné et Economou-Amilli in Lamprinou et al. 2016. Phytotaxa 282(3): 175',484,'[124]','','Species',NULL,'','ATHU-CY 3375','PH 00323987','Dim-light calcareous substrata, in caves','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(486,'Desertifilum','Dadheech et Krienitz 2012. Phycologia 51(3): 263',46,'[125]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(487,'Desertifium tharense','Dadheech et Krienitz 2012. Phycologia 51(3): 263',486,'[125]','','Species',NULL,'','B 400040620','CCAP 1420/4','desert biological soil crust','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(488,'Desertifilum salkalinema','Cai et Li 2017. Phytotaxa 262(3): 264',486,'[126]','nom. inval. (holotype not designated)','Species',NULL,'','','CHAB 7200','alkaline pool','',0,0,'',0,'active','0000-00-00 00:00:00',NULL),(489,'Coleofasciculus','Siegesmund, Johansen et Friedl 2008: 1575',44,'[127]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(490,'Coleofasciculus chthonoplastes','(Thuret ex Gomont) Siegesmund, Johansen et Friedl 2008: 1575',497,'','','Species',NULL,'','','SAG 2209','brackish &nbsp;to marine, nonterrestrial','',1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(491,'Geminocystis papuanica','Korelusová, Kaštovský et Komárek 2009. Journal of Phycolology 45:934',187,'[39]','','Species',NULL,'','BRNM HY 1409','','surface of wet soil in tropical rainy forests','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(492,'Geminocystis herdmanii','Korelusová, Kaštovský et Komárek 2009. Journal of Phycolology 45:933',187,'','','Species',NULL,'','BRNM HY1415','PCC 6308','planktic in oligotrophic lakes','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(493,'Geminobacterium','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 22',2287,'[129]','','Genus',NULL,'','','','','',0,1,NULL,0,'active','2021-05-07 12:30:51','admin'),(494,'Geminobacterium atlanticum','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 22',493,'[129]','','Species',NULL,'','CBFS A-073-1','LEGE 07459','epizoic on shells of the marine gastropod mollusc <em>Patella </em>sp.','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(495,'Hyella patelloides','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 24',213,'','','Species',NULL,'','CBFS A-075-1','LEGE 07179','epizoic or euendolithic on shells of the marine gastropod mollusc <em>Patella </em>sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(496,'Geitleribactron purpureum','Cantonati et Komárek 2014. Freswater Science 33: 550',185,'[130][131]','','Species',NULL,'','TR cLIM009 PHYTOB 796','','epilithic on stones in carbonate lake, 9-21 m depth','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(497,'Coleofasciculus','Siegesmund, Johansen et Friedl 2008. Journal of Phycology 44: 1575',44,'[127]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(498,'Coleofasciculus chthonoplastes','(Thuret ex Gomont) Siegesmund, Johansen et Friedl 2008. Journal of Phycology 44: 1575',497,'','','Species',NULL,'[890][891][892]','iconotype Gomont (1892), pl. 14, figs 5,8','SAG 2209','brackish to marine, nonterrestrial','',1,1,NULL,0,'active','2020-03-27 10:11:03','admin'),(499,'Godleya','Novis et Visnovsky 2011. Phytotaxa 22: 14',31,'[133]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(500,'Godleya alpina','Novis et Visnovsky 2011. Phytotaxa 22: 14',499,'[133]','','Species',NULL,'','CHR 610793','LCR-CY2','Alpine herbfield soil','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(501,'Acaryochloris marina','Miyashita et Chihara 2003. Journal of Phycology 39: 1249',426,'[46]','does not meet requiremets of art. 8.4 of the ICN','Species',NULL,'','','MBIC11017',NULL,NULL,1,0,'',0,'basionym','0000-00-00 00:00:00',NULL),(502,'Adrianema adriaticum','De Toni 1936. Noterelle di nomenclura algologica VIII.: 2',98,'[134]','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(503,'Tolypothrix pseudorexia','Novis et Visnovsky 2011. Phytotaxa 22: 14',332,'[133]','','Species',NULL,'','CHR 610792','LCR-CYTR','Aerophytic crust on greywacke rock surface, 1640 m, associated with alpine <em>Trentepohlia </em>sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(504,'Scytonematopsis maxima','Novis et Visnovsky 2011. Phytotaxa 22: 16',303,'[133]','','Species',NULL,'','CHR 610791','LCR-FBC','Alpine herbfield soil, 1640 m, associated with scattered Chionochloa sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(505,'Hormoscilla irregularis','Novis et Visnovsky 2011. Phytotaxa 22: 18',207,'[133]','','Species',NULL,'','CHR 610794','LCR-OSC2','Alpine herbfield soil, 1640 m, associated with scattered <em>Chionochloa </em>sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(506,'Phormidium arthurensis','Novis et Visnovsky 2011. Phytotaxa 22: 19',267,'[133]','','Species',NULL,'','CHR 610795','LCR-OSC4a','Alpine herbfield soil, 1640 m, associated with scattered <em>Chionochloa </em>sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(507,'Albrightia tortuosa','Copeland 1936. Ann. New York Acad. Sci. 36: 86',99,'','','Species',NULL,'','','','Lake','',1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(508,'Albrightia roraimae','Kaštovský, Fučíková, Hauer et Bohunická 2011. Fottea 11(1): 176',99,'[25]','','Species',NULL,'','BRNM HY 2260','','Benthic and periphytic among other filamentous cyanobacteria, in rock pools and on wet rocks','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(509,'Entophysalis arboriformis','Kaštovský, Fučíková, Hauer et Bohunická 2011. Fottea 11(1): 174',175,'[25]','','Species',NULL,'','BRNM HY 2259','','aerophytic, on wet walls among other cyanobacteria','[183]',0,1,NULL,0,'active','2019-05-24 18:53:19','admin'),(510,'Albrightia roraimae','Kaštovský, Fučíková, Hauer et Bohunická 2011. Fottea 11(1): 176',99,'[25]','','Species',NULL,'','BRNM HY 2260','','Benthic and periphytic among other filamentous cyanobacteria, in rock pools and on wet rocks','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(511,'Albrightia tortuosa','Copeland 1936. <span itemprop=\'name\'>Annals of the New York Academy of Sciences</span> 36: 86',99,'','','Species',NULL,'','','','lake','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(512,'Entophysalis arboriformis','Kaštovský, Fučíková, Hauer et Bohunická 2011. Fottea 11(1): 174',175,'[25]','','Species',NULL,'','BRMN HY 2259','','on wet walls among other cyanobacteria','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(513,'Geitleribactron crassum','Gold-Morgan, Montejano et Komárek 1996. Algological Studies 83: 266',185,'[136]','','Species',NULL,'','FCME BALE2438','','epiphytic on <em>​Cladophora</em>​ and <em>​Oedogonium</em>​​​','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(514,'Chamaecalyx calyculatus','Gold-Morgan, Montejano et Komárek 1996. Algological Studies 83: 268',122,'[136]','','Species',NULL,'','FCME PA 3490','','epihytic on <em>​Audouinella</em>','',0,1,NULL,0,'active','2019-04-16 02:52:50','admin'),(515,'Ammassolinea','Hašler, Dvořák, Poulíčková et Casamatta 2014. Fottea 14(2): 242',49,'[138]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(516,'Ammassolinea attenuata','Hašler, Dvořák, Poulíčková et Casamatta 2014. Fottea 14(2): 242',515,'[138]','','Species',NULL,'','OLM Botany 24: 9218','UPOC 61/2013','epipelic on mixed sediment of sand and organic detritus','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(517,'Eucapsis alpina','Clements et Shantz 1909.<em>&nbsp;</em>Minnesota Bot. Stud. 4: &nbsp;134',408,'[88]','','Species',NULL,'','Univ of Minnesota','','pond','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(518,'Elainella','Jahodářová, Dvořák et Hašler 2018. European Journal of Phycology 53(1): 42',1034,'[139]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:19:17','admin'),(519,'Elainella saxicola','Jahodářová, Dvořák et Hašler. European Journal of Phycology 53(1): 42',518,'[139]','','Species',NULL,'','OLM Botany 24: Lichens and others No. 9222','UPOC E1/2017','Ephemeral waterbody in the forest','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(520,'Trichocoleus desertorum','Mühlsteinová, Johansen et Pietrasiak 2014. Phytotaxa 163(5): 244',333,'[140]','','Species',NULL,'','BRY 37728','CCALA 1032','desert soils','[178]',0,1,'',0,'active','2019-04-16 11:50:50','admin'),(521,'Trichocoleus badius','(Johansen et Lowe) Mühlsteinová, Johansen et Pietrasiak 2014. Phytotaxa 163(5): 248',333,'[140]','','Species',NULL,'[231]','BRY C  37684','CRS-1','','[113]',0,1,NULL,0,'active','2020-04-20 14:42:57','admin'),(522,'Okeania','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1100',50,'[141]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(523,'Okeania hirsuta','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1101',522,'[141]','','Species',NULL,'','US 217947','PAB-10-FEB-10-1','mangrove, seagrass ﬂats at 2–3 m depth','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(524,'Okeania plumata','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1102',522,'[141]','','Species',NULL,'','US 217946','FK12-27','coral reef habitat at a depth of 10 m','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(525,'Okeania comitata','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1102',522,'[141]','','Species',NULL,'','US 217943','3L-OSC','epiphytically on the cyanobacterium <em>Moorea producens </em>strain 3L at 2–3 m depth','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(526,'Okeania erythroflocculosa','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1103',522,'[141]','','Species',NULL,'','US 217944','FFP12-1','shallow seagrass ﬂats','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(527,'Okeania lorea','Engene, Paul, Byrum, Gerwick, Thor et Ellisman 2013. Journal of Phycology 49: 1103',522,'[141]','','Species',NULL,'','US 217945','FK12-17','shallow coral reefs','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(528,'Moorena','Engene et Tronholm 2019. Notulae Algarum 122',44,'[142][545]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:32:46','admin'),(529,'Moorena producens','Engene et Tronholm 2019. Notulae Algarum 122',528,'[142][545]','species originally published under invalid name Moorea producens (Engene et al. 2012)','Species',NULL,'','BRNM HY-2364','3L','&nbsp;coral rubble and rocks at 2–3 m depth','',1,1,'',0,'active','2020-05-14 12:51:28','admin'),(530,'Moorena bouillonii','(L.Hoffmann &amp; Demoulin) Engene &amp; Tronholm 2019. Notulae Algarum 122',528,'[142][545]','','Species',NULL,'','LG V. Demoulin 7122 (sub Lyngbya bouilloni)','PNG5-198','coral reefs at a depth of 10 m. The colonies are found in association with the snapping shrimp (Alpheus frontalis).','',0,1,'',0,'active','2020-05-14 12:49:16','admin'),(531,'Oscillatoria gebhardtiana','Claus 1962. Hydrobiologia 19(2): 199',258,'[144]','','Species',NULL,'','','','cave','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(532,'Oscillatoria crassivaginata','Claus 1962. Hydrobiologia 19(2): 200',258,'[144]','','Species',NULL,'','','','cave','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(533,'Oscillatoria mauchiana','Claus 1962. Hydrobiologia 19(2): 200',258,'[144]','','Species',NULL,'','','','cave','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(534,'Palikiella hungarica','Claus 1962. Hydrobiologia 19(2): 202',259,'[144]','','Species',NULL,'','','','cave','[65]',1,0,NULL,0,'active','2019-04-16 02:53:18','admin'),(535,'Palikiella abaligetiensis','Claus 1962. Hydrobiologia 19(2): 203',259,'[144]','','Species',NULL,'','','','cave','[65]',0,0,NULL,0,'active','2019-04-16 02:53:48','admin'),(536,'Symploca lacrimans','Claus 1962. Hydrobiologia 19(2): 203',324,'[144]','','Species',NULL,'','','','cave','',0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(537,'Stigonema anomalum','Blanchard 1913. Rhodora 15: 194',321,'[10]','','Species',NULL,'','','','freshwater, free floating among other algae','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(538,'Stigonema medium','Blanchard 1913. Rhodora 15: 196',321,'','','Species',NULL,'','','','freshwater, forming soft sod among other algae','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(539,'Schizothrix pulvinata','Kützing ex Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 294',300,'','','Species',NULL,'','','','freshwater, on stones and wood','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(540,'Schizothrix fasciculata','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 294',300,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(541,'Schizothrix rubella','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(542,'Schizothrix cresswellii','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(543,'Schizothrix lacustris','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(544,'Schizothrix vaginata','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(545,'Schizothrix tinctoria','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(546,'Schizothrix mexicana','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(547,'Schizothrix penicillata','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','','freshwater','[59]',0,1,NULL,1,'active','2020-02-18 13:14:54','admin'),(548,'Schizothrix calcicola','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(549,'Schizothrix lateritia','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(550,'Schizothrix coriacea','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(551,'Schizothrix lardacea','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(552,'Schizothrix arenaria','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 295',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(553,'Schizothrix fragilis','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(554,'Schizothrix rubra','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(555,'Schizothrix friesii','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(556,'Schizothrix chalybea','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(557,'Schizothrix thelephoroides','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(558,'Schizothrix purpurascens','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(559,'Schizothrix mulleri','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 321',300,'[145]','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>wet or sandy soil or </span><span title=\'\'>flooded <span lang=\'en\'><span title=\'\'>places, near &nbsp;Fontainebleau</span></span></span></span>','[59]',0,1,'',0,'active','2020-02-17 13:29:30','admin'),(560,'Schizothrix beccarii','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(561,'Schizothrix lamyi','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(562,'Schizothrix fuscescens','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 324',300,'[145]','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 08:24:51','admin'),(563,'Schizothrix heufleri','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(564,'Schizothrix braunii','Gomont 1892. Annales des Sciences Naturelles, Botanique, Série 7, 15: 296',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(565,'Nodosilinea','Perkenson et Casamatta 2011. Journal of Phycology 47: 1404',2544,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:33:18','admin'),(566,'Leptolyngbya nodulosa','Li et Brand 2007. Phycologia 46(4): 397',225,'[147]','','Species',NULL,'','UTEX 2910 (cryopreserved)','UTEX 2910','marine','',0,1,'',0,'active','2019-07-17 11:25:42','admin'),(567,'Nodosilinea nodulosa','(Li et Brand) Perkenson et Casamatta 2011. Journal of Phycology 47: 1405',565,'','','Species',NULL,'','','UTEX 2910',NULL,NULL,1,1,'clades:566',0,'active','2019-07-17 11:27:58','admin'),(568,'Nodosilinea epilithica','Perkenson et Casamatta 2011. Journal of Phycology 47: 1405',565,'[146]','','Species',NULL,'','BRY 37707','Kováčik 1998/7','biofilm on the wall','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(569,'Phormidium bijugatum','Kongisser 1924. Trudy Leningradskogo obščestva jestestvoispytatelej 54(<em>3</em>): 70',267,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(570,'Nodosilinea bijugata','(Kóngisser) Perkenson et Kováčik 2011. Journal of Phycology 47: 1405',565,'[146]','','Species',NULL,'','','1986/5a',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(571,'Nodosilinea conica','Perkenson et Johansen 2011. Journal of Phycology 47: 1407',565,'[146]','','Species',NULL,'','BRY 37708','SEV4-5-c1','desert soil','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(572,'Nodosilinea chupicuarensis','Vázquez-Martínez, Gutierrez-Villagomez and Molina-Torres 2018. Phytotaxa 334(2): 171',565,'[128]','','Species',NULL,'','MEXU 4813','','stone surface','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(573,'Chondrocystis','Lemmermann 1899. A<span itemprop=\'name\'>bhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen 16: 353</span>',16,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(574,'Chondrocystis schauinslandii','Lemmermann 1899. A<span itemprop=\'name\'>bhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen 16: 353</span>',573,'[95]','','Species',NULL,'','','','lagoon','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(575,'Coelosphaeriopsis halophila','Lemmermann 1899. A<span itemprop=\'name\'>bhandlungen herausgegeben vom Naturwissenschaftlichen Verein zu Bremen 16: 353</span>',421,'[95]','','Species',NULL,'','','','lagoon','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(576,'Cyanosaccus piriformis','Lukas et Golubić 1981. Journal of Phycology 17: 225',158,'[149]','','Species',NULL,'','FH CYS298H','','in mollusk shells','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(577,'Mojavia pulchra','Řeháková et Johansen 2007. Phycologia 46 (5): 490',248,'[50]','','Species',NULL,'','BRY C-37693','CCALA 691','subaerophytic sandy desert soil','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(578,'Ancylothrix','Martins et Branco 2016. &nbsp;International Journal of Systematic and Evolutionary Microbiology 66: 2402',49,'[151]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(579,'Ancylothrix rivularis','Martins et Branco 2016. &nbsp;International Journal of Systematic and Evolutionary Microbiology 66: 2402',49,'[151]','','Species',NULL,'','SJRP 31538','','stream benthos','',1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(580,'Ancylothrix','Martins et Branco 2016. &nbsp;International Journal of Systematic and Evolutionary Microbiology 66: 2402',49,'[151]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(581,'Ancylothrix rivularis','Martins et Branco 2016. &nbsp;International Journal of Systematic and Evolutionary Microbiology 66: 2402',580,'[151]','','Species',NULL,'','SJRP 31538','8PC','stream benthos','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(582,'Ancylothrix terrestris','Martins et Branco 2016. &nbsp;International Journal of Systematic and Evolutionary Microbiology 66: 2403',580,'[151]','','Species',NULL,'','SJRP 31539','10PC','soil and bark of trees','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(583,'Desertifilum fontinale','Dadheech, Mahmoud, Kotut et Krienitz 2014. Fottea 14(2): 133',486,'[152]','','Species',NULL,'','B 40 0040927','UTEX LB 2975','thermal spring','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(584,'Phormidium etoshii','Dadheech, Casamatta, Casper et Krienitz 2013. Fottea 13(2): 237',267,'[153]','','Species',NULL,'','B 40 0040890','','hyposaline water puddles, springs and wet soil','',0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(585,'Cyanospira rippkae','Florenzano, Sili, Pelosi et Vincenzini 1985. Archives of Microbiology 140: 305',160,'[154]','description does not meet rules of ICN neither ICNP','Species',NULL,'','','Mag II 702','alkaline soda lake','',0,0,NULL,0,'active','2022-03-22 14:20:03','admin'),(586,'Cyanospira capsulata','Florenzano, Sili, Pelosi et Vincenzini 1985. Archives of Microbiology 140: 305',160,'[154][610]','description does not meet rules of ICN neither ICNP','Species',NULL,'','CBFS A-047','Mag I 504','alkaline soda lake','',1,0,'',0,'active','2022-03-22 14:19:49','admin'),(587,'Gloeobacter kilaueensis','Saw, Schatz, Brown, Kunkel, Foster, Shick, Christensen, Hou, Wan et Donachie 2013. PLoS ONE 8(10): &nbsp;e76376, p. 8',189,'','','Species',NULL,'','US 217948','ATCC BAA-2537 = CCAP 1431/1 = ULC0316','in epilithic biofilm on the wall of a lava cave','[265]',0,1,'',0,'active','2019-06-06 11:27:11','admin'),(588,'Gloeobacter violaceus','Rippka, Waterbury et Cohen-Bazire 1974. Archives for Microbiology 100: 435',189,'','','Species',NULL,'','BRNM HY-2366','PCC 7421','wet walls','',1,1,'',0,'active','2019-04-11 20:07:38',NULL),(589,'Gloeothece linearis','Nägeli 1849. Gattungen der einzelliger Algen: 58',192,'[115]','','Species',NULL,'','iconotype Nägeli 1849, tab 1, G, fig. 2','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(590,'Prochlorococcus marinus','Chisholm, Frankel, Goericke, Olson, Palenik, Waterbury, West-Johnsrud et Zettler in Komárek et al. 2020. Fottea 20(2): 178',278,'[574]','','Species',NULL,'','CBFS A–122–1','CCMP 1375','deep euphotic zone in oceans','',1,1,'',0,'active','2021-05-27 13:41:35','admin'),(591,'Dapisostemon','Hentschke, Sant’Anna et Johansen 2016. Phytotaxa 245(2): 136',28,'[159]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(592,'Dapisostemon apicaliramis','Hentschke, Sant’Anna et Johansen 2016. Phytotaxa 245(2): 136',591,'[159]','','Species',NULL,'','SP 401441','CCIBt 3318','terrestrial biofilms on wood','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(593,'Aliinostoc','Bagchi, Bubey et Singh 2017. International Journal of Systematic and Evolutionary Microbiology 67(9): 3336',34,'[161]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(594,'Aliinostoc morphoplasticum','Bagchi, Bubey et Singh 2017. International Journal of Systematic and Evolutionary Microbiology 67(9): 3337',593,'[161]','','Species',NULL,'','MCC 3177 (cryopreserved strain)','MCC 3177','stagnant, eutrophic-polluted water, attached to the benthic rocks and other submerged substrates','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(595,'Neolyngbya','Caires, Sant’Anna et Nunes 2018. &nbsp;Molecular Phylogenetics and Evolution 120: 201',2413,'[162]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2022-01-14 13:16:11','admin'),(596,'Neolyngbya maris-brasilis','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 203',595,'[162]','','Species',NULL,'','ALCB 114380','','epipsammic or epilithic in tidal pools in mediolittoral zone','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(597,'Neolyngbya granulosa','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 204',595,'[162]','','Species',NULL,'','ALCB 114378','','&nbsp;epilithic in tidal pools in mediolittoral zone, occurring especially at the edges in these pools','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(598,'Neolyngbya irregularis','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 205',595,'[162]','','Species',NULL,'','ALCB 114382','','epipsammic in estuary','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(599,'Neolyngbya nodulosa','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 205',595,'[162]','','Species',NULL,'','ALCB 114383','','epilithic on rocky shore','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(600,'Neolyngbya arenicola','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 206',595,'[162]','','Species',NULL,'','ALCB 114386','','episamic in tidal pools in mediolittoral zone','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(601,'Neolyngbya tenuis','Caires, Sant’Anna et Nunes 2018. Molecular Phylogenetics and Evolution 120: 206',595,'[162]','','Species',NULL,'','ALCB 114390','','epilithic in protected reef region in mediolittoral zone','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(602,'Cronbergia amazonensis','Genuário, Sant Anna et Melo 2018. Algal Research 29: 239',141,'[163]','','Species',NULL,'','SP 470029','CMAA 1598','surface of freshwater from the Solimões River, Brazil','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(603,'Neowestioellopsis','Kabirnataj, Nemazadeh, Talebi, Tabatabaei et Singh 2018. Plant Systematics and Evolution 304: 508',32,'[165]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:13:45','admin'),(604,'Neowestiellopsis persica','Kabirnataj, Nemazadeh, Talebi, Tabatabaei et Singh 2018. Plant Systematics and Evolution 304: 508',603,'[165]','','Species',NULL,'','MCC 3377 (cryopreserved strain)','MCC 3377','soil of paddy field having no water','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(605,'Neowestiellopsis bilateralis','Kabirnataj, Nemazadeh, Talebi, Tabatabaei et Singh 2018. Plant Systematics and Evolution 304: 508',603,'[165]','','Species',NULL,'','MCC 3376 (cryopreserved strain)','MCC 3376','almost dried mat on the soil of paddy field devoid of any water','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(606,'Neosynechococcus sphagnicola','Dvořák, Hindák, Hašler et Hindáková 2014. Phytotaxa 170(1): 26',404,'[85]','','Species',NULL,'','OLM Botany 24: Lichenes and others No. 9217','CAUP A1101','facultatively endophytic inside hyaline cells of Sphagnum, sheaths of cyanobacteria, dead cells of desmids, carapaces of dead crustaceans, and solitary','[86]',1,1,NULL,0,'active','2019-04-16 02:55:12','admin'),(607,'Prochlorococcales','',1,'','','Order',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(608,'Schizothrix Group C','Hobit (test)',300,'','','Species group',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(609,'Chroogloeocystis siderophila','Brown, Mummey et Cooksey, 2005. FEMS Microbiology Ecology 52:&nbsp;',131,'[166]','no formal description in the paper','Species',NULL,'','','ATCC BAA-845 = NIES-1031 = CCAP 1419/1','wet biofilm in cement drainage culvert connecet to thermal spring','',1,0,NULL,0,'active','2020-07-13 10:25:26','admin'),(610,'Planktothix spiroides','Wang et Li 2013. Phycologia 52(4): 328',272,'[167]','','Species',NULL,'','HAB2013-0222','fs1','pond','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(611,'Annamia','Nguyen 2013. Phycologia 52(1): 34',2287,'[168]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-07 12:30:26','admin'),(612,'Annamia toxica','Nguyen 2013. Phycologia 52(1): 34',611,'[168]','','Species',NULL,'','C CAT2458','','freshwater plankton','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(613,'Iningainema','McGregor et Sendall 2017. Harmful algae 62:17',37,'[169]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(614,'Gloeomargarita lithophora','Moreira, Tavera, Benzerara, Skouri-Panet, Couradeau, Gérard, Fonta, &nbsp;Novelo, Zivanovic et López-García 2017. International Journal of &nbsp;Systematic and Evolutionary Microbiology 67: 657',400,'[81]','','Species',NULL,'','FCME PueAl-43a','CCAP 1437/1 and PMC 919.15','microbialite in alkaline lake','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(615,'Cyanomargarita','Shalygin, Shalygina et Johansen 2017. Journal of Phycology 53: 769',1713,'[170]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-10-08 10:58:28','admin'),(616,'Cyanomargarita melechinii','Shalygin, Shalygina et Johansen 2017. Journal of Phycology 53: 769',615,'[170]','','Species',NULL,'','BRY 37764','APA-RS9','cold, small, spring-fed, unpolluted, flowing stream in secondary, young forest with coniferous and deciduous trees, below the water surface on the mosses and stones (10 cm), pH 8.4.','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(617,'Cyanomargarita calcarea','Shalygin, Shalygina et Johansen 2017. Journal of Phycology 53: 772',615,'[170]','','Species',NULL,'','BRY 37768','GSE-NOS12- 04C','wet limestone wall, pH 7.9','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(618,'Dactylothamnos','Komárek, Genuário, Fiore et Elster 2015. Polar Biology 38: 480',40,'[171]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(619,'Dactylothamnos antarcticus','Fiore, Genuário et Komárek 2015. Polar Biology 38: 480',618,'[171]','','Species',NULL,'','iconotype p. 483, fig. 8','CENA 410','in seepages among other algae and cyanobacteria in littoral of streams and lakes and on wetted rocks, during Antarctic summer season','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(620,'Calothrix polaris','Komárek et Elster 2015. Polar Biology 38: 479',119,'[171]','','Species',NULL,'','iconotype p. 480, fig. 4','','epiphytic on mosses and filamentous algae, rarely epilithic, mostly in seepages, &nbsp;margins of small streams and lakes','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(621,'Hydrocoryne australis','Genuário, Fiore et Komárek 2015. Polar Biology 38: 483',212,'[171]','holotype insufficiently designated','Species',NULL,'','','CENA 398','in shallow pools and soil seepages, on edges of stagnant waters, streams and in littoral of lakes, coastal Antarctica','',0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(623,'Hydrocoryne quesadae','Genuário, Fiore et Komárek 2015. Polar Biology 38: 484',212,'[171]','','Species',NULL,'','iconotype p. 488, fig. 13','','&nbsp;In wet soils, margins of seepages, streams and lakes, subaerophytic','[2]',0,1,NULL,0,'active','2019-07-10 07:28:43','admin'),(624,'Hassallia andreassenii','Komárek, Nedbalová et Hauer 2012. Polar Biology 35: 768',200,'[172]','','Species',NULL,'','BRNM HY2361','CCALA 954','surface of stones in the littoral of the flat lake','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(625,'Hassallia antarctica','Komárek, Nedbalová et Hauer 2012. Polar Biology 35: 770',200,'[172]','','Species',NULL,'','BRNM HY2362','CCALA 957','shallow lake, found in stone crevices, being only loosely attached to the substrate','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(626,'Calothrix elsteri','Komárek, Nedbalová et Hauer 2012. Polar Biology 35: 764',119,'[172]','','Species',NULL,'','BRNM HY2360','CCALA 953','alkaline lake with stagnant water level','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(627,'Pseudoscillatoria coralii','Rasoulouniriana, Siboni, Ben-Dov, Kramarsky-Winter, Loya, Kushmaro 2009. Diseaeses of Aquatic Organisms 87:',442,'[108]','','Species',NULL,'','','BgP10_4S','surface of the coral Favia sp.','',1,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(628,'Leptolyngbya appalachiana','Johansen et Olsen 2008. Algological Studies 126: 24',225,'','','Species',NULL,'','BRY C 37679','GSM-SFF-MF60','quarzite seep wall','',0,1,NULL,1,'active','2019-05-29 12:57:07','admin'),(629,'Leptolyngbya badia','Johansen et Lowe 2008. Algological Studies 126: 26',225,'[173]','','Species',NULL,'','BRY C 37684','','quarzite seep wall','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(630,'Timaviella','Sciuto et Moro 2017. Cryptogamie, Algologie, 38(4): 318',1034,'[174]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-04-11 20:08:09',NULL),(631,'Timaviella circinata','Sciuto et Moro 2017. Cryptogamie, Algologie, 38(4): 319',630,'[174]','','Species',NULL,'','PAD A000629','ULC 401','wall in limestone cave','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(632,'Timaviella karstica','Sciuto et Moro 2017. Cryptogamie, Algologie, 38(4): 319',630,'[174]','','Species',NULL,'','PAD A000630','ULC 402','limestone cave wall','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(633,'Nephrococcus serbicus','Popović, Subakov Simić et Komárek 2016. Phytotaxa 282(2):138',253,'[175]','','Species',NULL,'','BEOU T0008','','biofilm on wall in limestone cave','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(652,'aaa','xxx',24,'','','Genus',NULL,'','','',NULL,NULL,0,0,'',1,'deleted','0000-00-00 00:00:00',NULL),(653,'bbbb','sss',24,'','','Genus',NULL,'[222][225][229]','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(654,'bbbb 111','ooo',24,'','','Species',NULL,'[230]','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(655,'bbbb 222','',24,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(656,'bbbb 111','ttt',24,'','','Species',NULL,'[223]','','',NULL,NULL,0,0,'',1,'deleted','0000-00-00 00:00:00',NULL),(657,'bbbb 222','qqq',24,'','','Species',NULL,'[224]','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(658,'bbbb 333','',24,'','','Species',NULL,'[226][228]','','','habbbitat 333','',0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(659,'bbb 444','',653,'','','Species',NULL,'[227]','','','Blato','',0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(660,'Chroococcidiopsis','Geitler 1933. Arch. Hydrobiol., Suppl. 12: 625.',23,'','','Genus','[59]','[12]','','',NULL,NULL,0,1,'',0,'active','2019-05-24 05:49:13','admin'),(661,'Chroococcidiopsis lichenoides','Villanueva, Hašler et Casamatta',660,'[176]','','Species',NULL,'','OLM Botany 24: Lichens and others, No. 9227','UPOC 165/2015','&nbsp;in consortia as a lichen on granite cemetery tombstones','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(662,'Brasilonema lichenoides','Hašler et Casamatta',118,'[176]','','Species',NULL,'','OLM Botany 24: Lichens and others, No. 9226','UPOC 168/2015','in consortia as a lichen on granite cemetery tombstones','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(663,'Cyanocatena','Hindák, 1975. Algolog. Stud. 13: 334',66,'[76]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(664,'Prochlorococcus','Chisholm, Frankel, Goericke, Olson, Palenik, Waterbury, West-Johnsrud et Zettler, 1992. Arch Microbiol 157:',63,'','','Genus',NULL,'','','',NULL,NULL,0,0,'',1,'active','2019-06-12 12:56:06','admin'),(665,'Chamaesiphonopsis','Fritsch, 1929. New Phytol. 28(3): 173',58,'[177]','','Genus',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-06-06 14:01:37','admin'),(666,'Neosynechococcus','Dvořák, Hindák, Hašler et Hindáková, 2014. Phytotaxa 170(1): 26',61,'[85]','','Genus',NULL,'','','',NULL,NULL,0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(667,'Phormidesmis','Turicchia, Ventura, Komárková et Komárek, 2009. Nova Hedwigia 89(1-2): 179',61,'[178]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(668,'Planktolyngbya','Anagnostidis et Komárek. Algolog, 1988. Stud. 50-53: 394',61,'[102]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(669,'Plectolyngbya','Taton, Wilmotte, Šmarda, Elster et Komárek, 2011. Polar Biol. 34: 184',61,'[56]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(670,'Plectolyngbya hodgsonii','Taton, Wilmotte, Šmarda, Elster et Komárek',669,'[56]','','Species',NULL,'','BRNM/HY 1406','ANT.LPR2',NULL,NULL,1,1,'',0,'active','2019-07-10 11:29:56','admin'),(671,'Leibleinia','Hoffmann, 1985. Crypt. Algol. 6(2): 77',61,'[179]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(672,'Halospirulina','Nübel at al., 2000. IJSEM: 50: 1273',56,'[180]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(673,'Halospirulina tapeticola','Nübel, Garcia-Pichel et Muyzer 2000. IJSEM 50: 1275',672,'','','Species',NULL,'','','CCC Baja-95 Cl. 2T',NULL,NULL,1,1,'',0,'active','0000-00-00 00:00:00',NULL),(674,'Spirulina','Turpin ex Gomont 1892, p. 249',12,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(675,'Cyanoaggregatum','Werner, Sant Anna et Azevedo, 2008. Revista Brasil. Bot. 31(3): 493-494',15,'[61]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(676,'Chalicogloea','Roldán, Ramírez, del Campo, Hernández-Mariné et Komárek, 2013. IJSEM 63: 2329',16,'[181]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(677,'Chalicogloea cavernicola','Roldán, Ramírez, del Campo, Hernández-Mariné et Komárek, 2013. IJSEM &nbsp;2329-2330',676,'[181]','','Species',NULL,'','BCN-Phyc 6164','COLL 3T; CCALA 975','','[88]',1,1,NULL,0,'active','2021-06-17 12:21:07','admin'),(678,'Anagnostidinema','Strunecký, Bohunická, Johansen et Komárek, 2017. Fottea 17(1): 119',2555,'[182]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:33:34','admin'),(679,'Kastovskya','Mühlsteinová, Johansen et Pietrasiak, Phytotaxa 163 (4): 219',44,'[183]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(680,'Kastovskya adunca','(Schwabe) Mühlsteinová, Johansen et Pietrasiak, Phytotaxa 163(4): 219-221',679,'[183]','','Species',NULL,'','','ATA6-11-RM4, CCALA 1025',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(681,'Kamptonema','Strunecký, Komárek et Šmarda 2014. Preslia 86: 203',49,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-25 10:34:25','admin'),(682,'Kamptonema animale','(Agardh ex Gomont) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 203',681,'[184]','','Species',NULL,'[600][634]','','CCALA 139','&nbsp;warm, thermal and sulphur springs, wet soils, rarely in puddles, in stagnant cold water, walls of greenhouses, widely distributed in temperate and tropical zones','',1,1,'clades:1196',0,'active','2019-11-15 13:24:31','admin'),(683,'Kamptonema pavlovskoense','(Elenkin) Strunecký, Komárek et Šmarda, Preslia 86: 203',681,'[184]','','Species',NULL,'','','','periphytic in stagnant and flowing','',0,1,'clades:1203',0,'active','2019-11-15 13:18:07','admin'),(684,'Kamptonema cortianum','(Meneghini ex Gomont) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 203',681,'[184]','','Species',NULL,'[635][636][637]','','','in thermal and mineral springs','',0,1,'clades:1198',0,'active','2019-11-15 13:24:50','admin'),(685,'Kamptonema okenii','(Agardh ex Gomont) Strunecký, Komárek et Šmarda, Preslia 86: 203',681,'[184]','','Species',NULL,'[651][652][653]','','','mineral and sulphur springs, rocky pools, ditches and rice fields (also in sewage), with high conductivity and usually alkaline wate','',0,1,'clades:1202',0,'active','2019-11-15 13:14:18','admin'),(686,'Kamptonema laetevirens','(Crouan ex Gomont) Strunecký, Komárek et Šmarda, Preslia 86: 204',681,'[184]','','Species',NULL,'[650]','','','salty and sulphur thermal','',0,1,'clades:1201',0,'active','2019-11-15 13:11:30','admin'),(687,'Kamptonema gebhardtianum','(Claus) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 204',681,'[184]','','Species',NULL,'[648]','','','calcareous substrate (Abaliget Caves)','[65]',0,1,'clades:531',0,'active','2019-11-15 13:25:52','admin'),(688,'Kamptonema chlorinum','(Kützing ex Gomont) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 204',681,'[184]','','Species',NULL,'[638][639][640][641][642]','','','benthic on organic mud, in sulphuretes, sometimes also in slightly salty','',0,1,'clades:1197',0,'active','2019-11-15 13:26:14','admin'),(689,'Kamptonema jasorvense','(Vouk) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 204',681,'[184]','','Species',NULL,'[649]','','','thermal','[87]',0,1,'clades:1200',0,'active','2019-11-15 13:27:08','admin'),(690,'Kamptonema formosum','(Bory ex Gomont) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 204',681,'[184]','','Species',NULL,'[643][644][645][646][647]','','','wet soils, shallow pools and ponds','',0,1,'clades:1199',0,'active','2019-11-15 13:25:16','admin'),(691,'Kamptonema proteus','(Skuja) Strunecký, Komárek et Šmarda, 2014, Preslia 86: 204',681,'[184]','','Species',NULL,'[654]','','','benthos and free floating in stagnant water, tropical species','',0,1,'clades:1204',0,'active','2019-11-15 13:23:30','admin'),(692,'LImnoraphis','Komárek, Zapomělová, Šmarda, Kopecký, Rejmánková, Woodhouse, Neilan et Komárková, 2013. Fottea 13(1): 45',2413,'[185]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-01-14 13:15:49','admin'),(693,'Microseira','Mc Gregor et Sendall, 2015. J. Phycol. 51: 112-113',2553,'[186]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:28:13','admin'),(694,'Chakia','Komárková, Zapomělová et Komárek, 2013. Fottea 13(2): 228',37,'[187]','','Genus',NULL,'','','',NULL,NULL,0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(695,'Ophiothrix','Sant Anna, Azevedo, Kaštovský et Komárek, 2010. Fottea 10(2): 218',37,'[52]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(696,'Chakia','Komárková, Zapomělová et Komárek, 2013. Fottea 13(2): 228',37,'[187]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-23 04:27:03','admin'),(697,'Ophiothrix','Sant Anna, Azevedo, Kaštovský et Komárek, 2010. Fottea 10(2): 218',37,'[52]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(698,'Cyanopiothrix','Molinari et Guiry 2021. Notulae Algarum 183: 3',37,'[52][621]','','Genus',NULL,'[1058]','','',NULL,NULL,0,1,'',0,'active','2022-08-11 14:22:57','admin'),(699,'Ifinoe','Lamprinou et Pantazidou in Lamprinou et al., 2011. IJSEM 61: 2909',39,'[150]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(700,'Iphinoe','Lamprinou et Pantazidou in Lamprinou et al., 2011. IJSEM 61: 2909',37,'[150]','','Genus',NULL,'','','',NULL,NULL,0,0,'',0,'active','2023-02-01 13:54:00','admin'),(701,'Loriellopsis','Hernández-Mariné et Canals in Lamprinou et al., 2011. IJSEM 61: 2910',39,'','','Genus',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','2019-07-22 08:59:46','admin'),(702,'Streptostemon','Sant Anna, Azevedo, Kaštovský et Komárek 2010. Fottea 10(2): 220',40,'[52]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-07 15:13:36','admin'),(703,'Toxopsis','Lamprinou, Skaraki, Kotoulas, Economou-Amilli et Pantazidou 2012. IJSEM 62: 2872',31,'[189]','holotype of the type species not unambiguously defined','Genus',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-04-07 16:01:01','admin'),(704,'Rhizonemataceae','Budel &amp; Kauff ex Lucking &amp; Barrie, The Lichenologisl 46(3): 264',9,'[190]','','Family',NULL,'','','',NULL,NULL,0,0,'',0,'active','2019-07-19 12:21:06','admin'),(705,'Rhizonema','Lucking et Barrie, 2014, &nbsp;The Lichenologist 46(3): 265',704,'','','Genus',NULL,'','','',NULL,NULL,0,0,'',0,'active','2019-06-13 07:32:40','admin'),(706,'Aetokthonos','Wilde et Johansen in Wilde et al. 2014, Phytotaxa 181 (5): 247',37,'[191]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-02-01 13:52:36','admin'),(707,'Calochaete','Hauer, Bohunická &amp; Mühlsteinová, Phytotaxa 109(1): 38',33,'[192]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(708,'Chrysosporum','Zapomelova, Skácelová, Pumman, Kopp et Janeček, 2012. &nbsp;Hydrobiologia 698: 359',25,'[193]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(709,'Cyanocohniella','Kaštovský, Berrendero, Hladil et Johansen 2014. Phytotaxa 181(5): 281-282',34,'[195]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-10-11 07:29:47','admin'),(710,'Desmonostoc','Hrouzek et Ventura, 2013, Fottea 13(2): 211',34,'[196]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(711,'Goleter','Miscoe et Johansen in Miscoe et al., 2016, Bibl. Phycol. 120: 92',34,'[111]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(712,'Goleter apudmare','Miscoe et Johansen, 2016, Biblioth. Phycol. 120: 92-93',711,'[111]','','Species',NULL,'','BISH 755086','HA4340-LM2','Collected from the wall of Maniniholo Cave. The area of the wall was relatively dry compared to other parts of the cave but was littered with slimy, tan to blue-green colonies.','[265]',1,1,NULL,0,'active','2019-07-08 14:29:18','admin'),(713,'Brasilonema burkei','Miscoe, Pietrasiak et Johansen, 2016, Biblioth. Phycol. 120: 88',118,'[111]','','Species',NULL,'','BISH 755080','HA4348-LM4',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(714,'Desmonostoc geniculatum','Miscoe, Pietrasiak et Johansen, 2016, Biblioth. Phycol. 120: 89',710,'[111]','','Species',NULL,'','BISH 755081','HA4343-LM1',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(715,'Desmonostoc muscorum','(Agardh ex Bornet et Flahault) Hrouzek et Ventura, Fottea 13(2): 211',710,'[196]','','Species',NULL,'','Agardh Herbarium 6154 (LD)','NIVA–CYA 818',NULL,NULL,1,1,'clades:919',0,'active','0000-00-00 00:00:00',NULL),(716,'Desmonostoc vinosum','Miscoe et Johansen 2016, Biblioth. Phycol. 120: 90-91',710,'','','Species',NULL,'','BISH 755083','HA7617-LM4',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(717,'Nostoc cavernicola','Miscoe et Johansen, Biblioth. Phycol. 120: 93-94',255,'[111]','','Species',NULL,'','BISH 755087','HA4349-LM2',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(718,'Stenomitos frigidus','(Fritsch) Miscoe et Johansen in Miscoe et al. , 2016. Biblioth. Phycol. 120: 86',481,'[111]','','Species',NULL,'[518][502]','','',NULL,NULL,0,1,'clades:1394',0,'active','2019-06-11 06:46:22','admin'),(719,'Stenomitos tremulus','(Johansen et Casamatta) Miscoe et Johansen, 2016, Biblioth. Phycol. 120: 86',481,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(720,'Chroococcidiopsis muralis','(Lagerheim in Wittrock et Nordstedt) Miscoe et Johansen 2016, Biblioth. Phycol. 120: 87',660,'[111]','','Species',NULL,'','BISH 755078','HA8275-LM2',NULL,NULL,0,1,'clades:1300',0,'active','2019-05-24 05:47:16','admin'),(721,'Pelatocladus','Johansen et Vaccarino in Miscoe et al. 2016, Biblioth. Phycol. 120: 94-95',32,'[111]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2020-04-01 14:40:21','admin'),(722,'Pelatocladus maniniholoensis','Johansen et Vaccarino in Miscoe et al. 2016, Biblioth. Phycol. 120: 94-95',721,'[111]','','Species',NULL,'','BISH 759444','HA4357-MV3','walls in a cave','[265]',1,1,NULL,0,'active','2019-07-10 08:34:25','admin'),(723,'Tolypothrix carrinoi','Miscoe, Pietrasiak et Johansen &nbsp;in Miscoe et al. 2016, Biblioth. Phycol. 120: 95-96',332,'[111]','','Species',NULL,'','BISH 755079','HA7290-LM1',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(724,'Anagnostidinema pseudacutissimum','(Geitler) Strunecký, Bohunická, Johansen et Komárek, 2017, Fottea 17(1): 119',678,'','Epitype: dry material CBFS A–057','Species',NULL,'','','CCALA 150',NULL,NULL,1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(725,'Anagnostidinema amphibium','(Agardh ex Gomont) Strunecký, Bohunická, Johansen et Komárek, 2017, Fottea 17(1): 119-121',678,'[182]','Epitype: dry material CBFS A-058','Species',NULL,'[238][240][239][241]','','RO–MK72',NULL,NULL,0,1,'clades:1075',0,'active','2022-03-25 08:23:23','admin'),(726,'Anagnostidinema acutissimum','(Kufferath) Strunecký, Bohunická, Johansen et Komárek, 2017, Fottea 17(1): 121',678,'','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(727,'Anagnostidinema carotinosum','',678,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(728,'Anagnostidinema pseudacutissimum','(Geitler) Strunecký, Bohunická, Johansen et Komárek, 2017, Fottea 17(1): 119',678,'[182]','','Species',NULL,'[236][237]','epitype CBFS A-057','CCALA150',NULL,NULL,1,1,'clades:1074',0,'active','0000-00-00 00:00:00',NULL),(729,'Anagnostidinema amphibium','(Agardh ex Gomont) Strunecký, Bohunická, Johansen et Komárek, 2017, Fottea 17(1): 119-121',678,'','Epitype: dry material CBFS A508','Species',NULL,'','','RO–MK72',NULL,NULL,0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(730,'Anagnostidinema acutissimum','Kufferath) Strunecký, Bohunická, Johansen et Komárek 2017, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1076',0,'active','0000-00-00 00:00:00',NULL),(731,'Anagnostidinema carotinosum','(Geitler) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'[242][243]','','',NULL,NULL,0,1,'clades:1077',0,'active','0000-00-00 00:00:00',NULL),(732,'Anagnostidinema deflexum','(W. et G.S.West) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1078',0,'active','0000-00-00 00:00:00',NULL),(733,'Anagnostidinema epiphloeophyticum','(Anagnostidis) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1080',0,'active','0000-00-00 00:00:00',NULL),(734,'Anagnostidinema exile','(Skuja) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1081',0,'active','0000-00-00 00:00:00',NULL),(735,'Anagnostidinema ionicum','(Skuja) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1082',0,'active','0000-00-00 00:00:00',NULL),(736,'Anagnostidinema lacus–solaris','(Campbell et Golubic) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1083',0,'active','0000-00-00 00:00:00',NULL),(737,'Anagnostidinema lemmermannii','(Woloszynska) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1084',0,'active','0000-00-00 00:00:00',NULL),(738,'Anagnostidinema tenue','(Anisimova) Strunecký, Bohunická, Johansen, Čapková, Raabová, Dvořák et Komárek, Fottea 17(1): 121',678,'[182]','','Species',NULL,'[244]','','',NULL,NULL,0,1,'clades:1085',0,'active','0000-00-00 00:00:00',NULL),(739,'Wilmottia murrayi','(W. et G.S.West) Strunecký, Komárek et Elster 2011, Fottea 11(1): 63',343,'[54]','','Species',NULL,'[269][270]','BRNM 2334HY','CCALA 843 (KGI28)','aerophytic, whale bones, King George Island','',1,1,'clades:1208',0,'active','2020-03-31 08:00:55','admin'),(740,'Wilmottia stricta','Machado-de-Lima, Martins et Branco 2017, Phytotaxa 307(1): 51',343,'[198]','','Species',NULL,'','SJRP 31580!','16PC','Talhadinho stream, municipality of São Jose do Rio Preto, São Paulo State','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(741,'Johanseninema constrictum','(Szafer) Hašler, Dvořák et Poulíčková 2014, Preslia 86: 293',436,'[103][104]','','Species',NULL,'[254][253][255]','','','Epipelic species that occurs in muddy sediments, often with organic detritus, in freshwater','',1,1,'clades:1098',0,'active','0000-00-00 00:00:00',NULL),(742,'Planktothricoides raciborskii','(Woloszynska) Suda &amp; Watanabe 2002, IJSEM 52: 1593-1594',271,'[55]','','Species',NULL,'[655]','','NIES 207T',NULL,NULL,1,1,'clades:895',0,'active','2019-11-18 13:55:00','admin'),(743,'Planktothricoides attenuata','Komárek et Komárková-Legnerová 2007, Hoehnea 34(1): 54',271,'[199]','','Species',NULL,'','WAT5.1','','freshwater, planktic','[180]',0,1,'',0,'active','2019-11-18 11:41:57','admin'),(744,'Macrospermum volzii','Komárek 2008, Fottea 8(1): 82',236,'','','Species',NULL,'','','',NULL,NULL,1,1,'clades:917',0,'active','2019-04-17 17:32:13','admin'),(745,'Macrospermum fuellebornii','(Schmidle) Komárek 2008, Fottea 8(1): 82',236,'[29]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:914',0,'active','0000-00-00 00:00:00',NULL),(746,'Macrospermum mysorense','(Gonzalves et Kamat) Komárek 2008, Fottea 8(1): 82',236,'[29]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:915',0,'active','0000-00-00 00:00:00',NULL),(747,'Macrospermum unisporum','&nbsp;(Gardner) KOmárek 2008, Fottea 8(1): 82',236,'[29]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:916',0,'active','0000-00-00 00:00:00',NULL),(748,'Cronbergia siamensis','(Antarikanonda) Komárek, Zapomelová et Hindák 2010, Crypt. Algol. 31(3): 329,332',141,'[37]','','Species',NULL,'','BRNM HY-2333','CCALA 756',NULL,NULL,1,1,'clades:921',0,'active','0000-00-00 00:00:00',NULL),(749,'Cronbergia paucicellularis','Komárek, Zapomelová et Hindák 2010, Crypt. Algolog. 31(3): 332-333',141,'[37]','','Species',NULL,'','','','metaphyton on small polls in the Slovakian National Nature Reserve Šúr and blackwater Čičov oxbow','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(750,'Cronbergia planctonica','(Cronberg) Komárek, Zapomelová &amp; Hindák 2010, Crypt. Algolog. 31(3): 333',141,'[37]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:922',0,'active','0000-00-00 00:00:00',NULL),(751,'Sphaerospermopsis reniformis','(Lemmermann) Zapomělová, Jezberová, Hrouzek, Hisem, Řeháková et Komárková 2010, J. Phycol. 46: 415',314,'','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','0000-00-00 00:00:00',NULL),(752,'Sphaerospermopsis aphanizomenoides','&nbsp;(Forti) Zapomělová, Jezberová, Hrouzek, Hisem, Řeháková et Komárková 2010, J. Phycol. 46: 415',314,'[63]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(753,'Sphaerospermopsis kisseleviana','(Elenkin) Zapomělová, Jezberová, Hrouzek, Hisem, Řeháková et Komárková 2010, J. Phycol. 46: 415',314,'[63]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(754,'Cuspidothrixlr tropicalis','(Horecká et Komárek) Rajaniemi, Komárek, Willame, Kaštovská, Hoffmann et Sivonen, 2005, Algolog. Stud. 117: 388',142,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(755,'Cuspidothrix elenkinii','(Kiselev) Rajaniemi, Komárek, Willame, Kaštovská, Hoffmann et Sivonen, 2005, Algolog. Stud. 117: 389',142,'[48]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(756,'Cuspidothrix capricorni','(Cronberg et Komárek) Rajaniemi, Komárek, Willame, Kaštovská, Hoffmann et Sivonen, 2005, Algolog. Stud. 117: 389',142,'[48]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(757,'Cuspidothrix ussatschevii','(Proskina-Lavrenko) Rajaniemi, Komárek, Willame, Kaštovská, Hoffmann et Sivonen, 2005, Algolog. Stud. 117: 389',142,'[48]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(758,'Cuspidothrix issatschenkoi','(Usačev) Rajaniemi, Komárek, Willame, Kaštovská, Hoffmann et Sivonen, 2005, Algolog. Stud. 117: 388',142,'[48]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','0000-00-00 00:00:00',NULL),(759,'Chrysosporum bergii','(Ostenfeld) Zapomělová, Skácelová, Pumann, Kopp et Janeček 2012, Hydrobiologia 698: 359',708,'[193]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1205',0,'active','0000-00-00 00:00:00',NULL),(760,'Chrysosporum ovalisporum','&nbsp;(Forti) Zapomělová, Skácelová, Pumann, Kopp et Janeček 2012, Hydrobiologia 698: 359',708,'[193]','','Species',NULL,'','','','Planktic in freshwaters, but usually in water with higher conductivity and slightly saline conditions','',0,1,'clades:1206',0,'active','0000-00-00 00:00:00',NULL),(761,'Chrysosporum minor','(Kiselev) Komárek 2012, Fottea 12(1): 141',708,'[200]','','Species',NULL,'','','','Planktic in halophilic lakes, reservoirs with higher conductivity and in relict-lakes','',0,1,'clades:1207',0,'active','0000-00-00 00:00:00',NULL),(762,'Calochaete cimrmanii','Hauer, Bohunická &amp; Mühlsteinová 2013, Phytotaxa 109(1): 38',707,'[192]','','Species',NULL,'','CBFS! A–015','CCALA 1012','Surface soil in “páramo”','[96]',1,1,NULL,0,'active','2019-07-08 13:46:02','admin'),(763,'Aetokthonos hydrillicola','Wilde et Johansen, 2014, Phytotaxa 181(5): 247-248',706,'[191]','','Species',NULL,'','US Algal collection #217986','CCALA 1050',NULL,NULL,1,1,'',0,'active','0000-00-00 00:00:00',NULL),(764,'Rhizonema interruptum','Lücking &amp; Barrie, 2014, &nbsp;The Lichenologists 46(3): 265-266',705,'[190]','insufficient holotype specification','Species',NULL,'','','',NULL,NULL,1,0,'',0,'active','2019-06-13 07:51:36','admin'),(765,'Toxopsis calypsus','Lamprinou, Skaraki, Kotoulas, Economou-Amili &amp; Pantazidou, 2012, IJSEM',703,'[189]','holotype not unambiguously defined','Species',NULL,'','ATHU-CY 3314, PH1095565','','cave','[62]',1,0,'',0,'active','2020-04-07 16:01:23','admin'),(766,'Streptostemon capitatus','Sant Anna, Azevedo, Kaštovský et Komárek 2010, Fottea 10(2): 224',702,'[52]','','Species',NULL,'','SP 400882','','Blackish flat or tufty colonies on lateritic soils in tropical forest “Mata Atlântica”; near Paranapiacaba and São Paulo, SP,','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(767,'Streptostemon lutescens','Sant Anna, Azevedo, Kaštovský et Komárek, 2010, Fottea 10(2): 224',702,'[52]','','Species',NULL,'','SP 400883','','Subaerophytic on stones in tropical forests; near Jureia, SP,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(768,'Spirirestis rafaelensis','Flechtner et Johansen in Fletchner et al. 2002, Nova Hedwigia 74(1—2): 7',315,'[201]','','Species',NULL,'','BRY C 35162','SRS70','desert soil surface, hanging plateau below Wedge Overlook, San Rafael Swell, Emery County, Utah','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(769,'Loriellopsis cavernicola','Hernández-Mariné et Canals in Lamprinou et al 2011, IJSEM 61: 2910',701,'','holotype not properly designated','Species',NULL,'','BCN-Phyc 6000, PH 1089025','LF-B5','Cave ‘Papellona’&nbsp;','',1,0,'',0,'active','2019-10-04 07:01:10','admin'),(770,'Iphinoe spelaeobios','&nbsp;Lamprinou et Pantazidou in Lamprinou et al. 2011, IJSEM 61: 2909',700,'[150]','holotype not properly designated','Species',NULL,'','ATHU-CY 3313M, PH 1088600','LO2-B1','cave ‘Koutouki’, cave ‘Kastria’&nbsp;','',1,0,'',0,'active','2019-10-04 07:01:37','admin'),(771,'Cyanopiothrix epidendron','(Sant Anna, Azevedo, Kaštovský et Komárek) Molinari et Guiry 2021. Notulae Algarum 183: 3',698,'[52]','','Species',NULL,'','SP 400881','','On mosses and liverworths on bark of trees (Sapium sp.) in tropical forest Mata Atlântica; near Paranapiacaba SP,','',1,1,'synonyms:1059',0,'active','2022-08-11 14:24:36','admin'),(772,'Cyanopiothrix epibryos','(Komárek) Molinari et Guiry 2021. Notulae Algarum 183: 3',698,'[621]','','Species',NULL,'','','','Creeping on submersed substrates (mostly mosses and plants) in acidic, not polluted pools (“restingas”) near coast of SE Brazil, near the edge of tropical forest; near Ubatuba, SP,','',0,1,'synonyms:1060',0,'active','2022-08-11 14:26:05','admin'),(773,'Cyanopiothrix hansgirgii','(Schmidle) Molinari et Guiry 2021. Notulae Algarum 183: 3',698,'','','Species',NULL,'','','','On bark of trees; known from E India (near Poona) and central (equatorial) Africa','',0,1,'synonyms:1061',0,'active','2022-08-11 14:25:41','admin'),(774,'Chakia ciliosa','Komárková , Zapomělová et Komárek 2013, Fottea 13(2): 228',696,'[187]','','Species',NULL,'','BRNM HY2367','CCALA No. 1015','Freshwater, originally periphytic, growing among cyanobacteria and algae forming mats at the bottom of oligotrophic tropical and subtropical alkaline marshes.','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(775,'Chakia cubana','(Komárek) Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017, Nova Hedwigia 105(3-4): 452',696,'[553]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1132',0,'active','2020-08-21 13:13:43','admin'),(776,'Brasilonema bromeliae','Fiore, Sant Anna, Azevedo, Komárek, Kaštovský, Sulek et Lorenzi 2007, J. Phycol. 43: 796',118,'','','Species',NULL,'','BRNM  1332','SPC951','In the inner side of leaves of bromeliads and on environmental wooden substrates in a greenhouse of the Botanical Garden in Sa˜o Paulo','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(777,'Brasilonema epidendron','Sant Anna et Komárek 2011, Rev. Bras. Bot. 34(1): 52-54',118,'','','Species',NULL,'','BRNM HY 1333','','Subaerophytic, corticolous or on old wooden substrates in Atlantic Forest, Juréia,','',0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(778,'Brasilonema angustatum','Vaccarino et Johansen, 2012, J. Phycol. 48(5): 1180',118,'[204]','','Species',NULL,'','BISH-751683','HA4187- MV1','Terrestrial, in moss.Moleka Trail, Round Top Drive, Manoa Valley, Oahu, Hawaii,','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(779,'Brasilonema ornatum','Sant Anna et Komárek in Sant Anna et al, 2011, Rev. Bras. Bot. 34(1): 54',118,'[203]','','Species',NULL,'','','','Subaerophytic, on bark of trees among mosses and lichens. Campos do Jordão, SP','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(780,'Brasilonema roberti-lamii','(Bourrelly) Sant’Anna et Komárek in Sant Anna et al. 2011, Rev. Brasil. Bot. 34(1): 56',118,'[203]','','Species',NULL,'','','','Aerophytic','',0,1,'clades:784',1,'deleted','0000-00-00 00:00:00',NULL),(781,'Brasilonema sennae','(Komárek) Sant’Anna et Komárek in Sant Anna et al., 2011, Rev. Brasil. Bot. 34(1): 57, 59',662,'[203]','','Species',NULL,'','','CENA114','From wetted subaerophytic stony and iron substrates near springs, vicinity of Paranapiacaba, SP','',0,1,'clades:785',1,'deleted','0000-00-00 00:00:00',NULL),(782,'Brasilonema terrestre','Sant Anna et Komárek in Sant Anna et al. 2011, Rev. Brasil. Bot. 34(1): 59',118,'[203]','','Species',NULL,'','','CENA 116','Subaerophytic on concrete, &nbsp;SP, Cardoso Island','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(783,'Brasilonema tolantongensis','Becera-Absalón et Montejano in Becera-Absalón et al, 2013, Fottea 13(1): 27',118,'[205]','','Species',NULL,'','','Tolantongo','subtropical, subaerophytic environments, on wet limestone walls near runoffs. Tolantongo in the state of Hidalgo','',0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(784,'Tolypothrix roberti-lamyi','Bourrelly in Bourrelly &amp; Manguin 1952, p. 151',332,'[206]','','Species',NULL,'','','',NULL,NULL,0,0,'',0,'basionym','0000-00-00 00:00:00',NULL),(785,'Camptylonemopsis sennae','Komárek 2003, Preslia 75: 225',120,'[28]','','Species',NULL,'','BRNM HY 1203','','Subaerophytic on stony (rarely also metallic) subshates, in periodical shallow streams, on the edge of streaming water, near Paranapiacaba, SP state','',0,1,NULL,0,'basionym','2019-06-06 06:54:32','admin'),(786,'Brasilonema sennae','&nbsp;(Komárek) Sant’Anna et Komárek 2011, Rev. Brasil. Bot. 34(1): 57',118,'[203]','','Species',NULL,'','','CENA114','wetted subaerophytic stony and iron substrates near springs, &nbsp;vicinity of Paranapiacaba, SP','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(787,'Brasilonema roberti-lamyi','(Bourrelly) Sant’Anna et Komárek, 2011, Rev. Brasil. Bot. 34(1): 56',118,'[203]','','Species',NULL,'','','','Aerophytic','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(788,'Brasilonema ornatum','Sant’Anna et Komárek in Sant Anna et al. 2011, Rev. Brasil. Bot. 34(1): 54',118,'[203]','','Species',NULL,'','','','Subaerophytic, on bark of trees among mosses and lichens. Campos do Jordão, SP&nbsp;','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(789,'Brasilonema terrestre','Sant’Anna et Komárek in Sant Anna et al. 2011, Rev. Brasil. Bot. 34(1): 59',118,'[203]','','Species',NULL,'','','CENA116','Subaerophytic on concrete. Cardoso Island, SP','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(790,'Brasilonema epidendron','Sant’Anna et Komárek in Sant Anna et al. 2011, Rev. Brasil. Bot. 34(1): 52',118,'[203]','','Species',NULL,'','BRNM HY 1333','','Subaerophytic, corticolous or on old wooden substrates in Atlantic Forest. Juréia, SP','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(791,'Brasilonema tolantongensis','Becerra–Absalón et Montejano in Becera-Absalón et al., 2013, Fottea 13(1): 27',118,'[205]','','Species',NULL,'','iconotype Fig. 2','TOLANTONGO','on wet limestone walls near runoffs, Tolantongo, state of Hidalgo','',0,1,NULL,0,'active','2019-07-19 13:24:08','admin'),(792,'Brasilonema angustatum','Vaccarino et Johansen 2012, J. Phycol. 48: 1180',118,'[204]','','Species',NULL,'','HA4187-MV1, BISH-751683','HA4187-MV1','Terrestrial, in moss; Moleka Trail, Round Top Drive, Manoa Valley, Oahu, Hawaii,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(793,'Brasilonema octagenarum','Aguiar, Fiore, Franco, Ventrella, Lorenzi, Vanetti et Alfenas 2008, J. Phycol. 44: 1325',118,'[71]','','Species',NULL,'','BRNM HY 1416','UFV-E1','Epiphytic, covering leaves, stems, and apical buds of young E. grandis plants in a nursery garden in Timo´teo City, Minas Gerais,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(794,'Brasilonema burkei','Miscoe, Pietrasiak et Johansen 2016, Biblioth. Phycol. 120: 88',118,'[111]','','Species',NULL,'','BISH 755080','HA4348-LM4','on the damp rock walls, in the entrance of th cave, Maniniholo Cave, Hawaii','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(795,'Microseira wollei','(Farlow ex Gomont) G.B.McGregor &amp; Sendall ex Kenins',693,'[207][186]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2021-06-17 12:45:33','admin'),(796,'Limnoraphis hieronymusii','(Lemmermann) Komárek, Zapomělová, Šmarda, Kopecký, Rejmánková, Woodhouse, Neilan et Komárková 2013, Fottea 13(1):45, 47',692,'[185]','','Species',NULL,'','','N 929,','freshwater plankton','',1,1,'clades:797',0,'active','0000-00-00 00:00:00',NULL),(797,'Lyngbya hieronymusii','Lemmermann &nbsp;1905, Forschungsber. biol. Stat. Plőn 12: 146',234,'[208]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-05-24 10:25:42',NULL),(798,'Limnoraphis birgei','(G.M.Smith) Komárek, Zapomělová, Šmarda, Kopecký, Rejmánková, Woodhouse, Neilan et Komárková 2013, Fottea 13(1): 47',692,'[185]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:801',0,'active','0000-00-00 00:00:00',NULL),(799,'Limnoraphis cryptovaginata','(Škorbatov) Komárek, Zapomělová, Šmarda, Kopecký, Rejmánková, Woodhouse, Neilan et Komárková 2013, Fottea 13(1): 47',692,'[185]','','Species',NULL,'[267]','','KUTNAR',NULL,NULL,0,1,'clades:802',0,'active','0000-00-00 00:00:00',NULL),(800,'Limnoraphis robusta','(Parakutty) Komárek, Zapomělová, Šmarda, Kopecký, Rejmánková, Woodhouse, Neilan et Komárková 2013, Fottea 13(1):47',692,'[185]','','Species',NULL,'[268]','BRNM HY 2365','CCALA 966',NULL,NULL,0,1,'clades:803',0,'active','0000-00-00 00:00:00',NULL),(801,'Lyngbya birgei','G.M. Smith, 1916, Bull. Torrey Bot. Club 43(9): 482',234,'[209]','','Species',NULL,'','','','plankton, Mendosa, Monona, Kegonsa lakes, Wisconsin','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(802,'Lyngbya cryptovaginata','Škorbatov 1923, Not. Syst. Inst. Crypt. Horti Petrop. 2(6): 88',234,'[214]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(803,'Lyngbya hieronymusii f. robusta','Parakutty 1940, Proc. Ind. Acad. Sci. 11: 123',234,'[210]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(804,'Lyngbya robusta .','(Parakutty) Komárek et Komárková–Legnerová 2007, Hoehnea 34(1): 55',234,'[199]','','Species',NULL,'','','',NULL,NULL,0,0,'',1,'deleted','0000-00-00 00:00:00',NULL),(805,'Planktothrix cryptovaginata','(Škorbatov) Anagnostidis et Komárek 1988, Algol. Stud. 50–53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:802',1,'active','2020-04-20 08:12:16','admin'),(806,'Phormidiochaete balearica','(Bornet &amp; Flahault ex Forti) Komárek in Anagnostidis 2001: 375',266,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:807',0,'active','0000-00-00 00:00:00',NULL),(807,'Calothrix balearica','Bornet et Flahault ex Bomet et Flahault 1886, Ann. Sci. Nat., VIl. Bot., 3: 348',119,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(808,'Phormidiochaete fusca','(Starmach) Komrárek in Anagnostidis 2001, Preslia 73(4): 375',266,'[9]','','Species',NULL,'','','',NULL,NULL,0,0,'clades:811',0,'active','0000-00-00 00:00:00',NULL),(809,'Phormidiochaete nordstedtii','(Bornet &amp; Flahault ex De Toni) Komárek &nbsp;in Anagnostidis 2001, Preslia 73(4): 375',266,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:812',1,'active','2019-06-13 06:24:37','admin'),(810,'Phormidiochaete crustacea','(Borzì ex Bornet et Flahault) Bohunická et Johansen',266,'[11]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(811,'Homoeothrix fusca','Starmach 1934, Acta Soc. Bot Poloniae 11(3): 294-295',205,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(812,'Dichothrix nordstedtii','Bornet et Flahault ex Bornet et Flahault 1886, Ann. Sci. Nat., VIL Bot., 3: 374,',171,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(813,'Tychonema bornetii','(Zukal) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'[628]','','',NULL,NULL,0,1,'clades:823',0,'active','2019-11-14 13:13:44','admin'),(814,'Tychonema bourrellyi','(Lund) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:824',0,'active','0000-00-00 00:00:00',NULL),(815,'Tychonema decoloratum','(G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:825',0,'active','0000-00-00 00:00:00',NULL),(816,'Tychonema exospirum','(Skuja) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'[629]','','',NULL,NULL,0,1,'clades:826',0,'active','2019-11-14 13:17:38','admin'),(817,'Tychonema granulatum','&nbsp;(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'','','Species',NULL,'','','',NULL,NULL,0,1,'clades:827',1,'active','2019-11-14 14:01:14','admin'),(818,'Tychonema griseo-violaceum','(Skuja) Anagnostidis &amp; Komárek 1988, Algolog. STud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:828',1,'active','2019-11-14 14:15:28','admin'),(819,'Tychonema ingricum','&nbsp;(Woronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:829',1,'active','2019-11-14 14:26:26','admin'),(820,'Tychonema rhodonema','(Skuja) Anagnostidis &amp; Komárek 1988, Algolog. STud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:830',0,'active','0000-00-00 00:00:00',NULL),(821,'Tychonema sequanum','(Couté) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:831',0,'active','0000-00-00 00:00:00',NULL),(822,'Tychonema tenue','(Skuja) K.Anagnostidis &amp; J.Komárek 1988, Algolog. Stud. 50-53: 413',338,'[102]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:832',0,'active','0000-00-00 00:00:00',NULL),(823,'Lyngbya bornetii','Zukal 1894, Ber. Deutsch. Bot. Gess. 12: 260',234,'[211]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:05:03','admin'),(824,'Oscillatoria bourrellyi','Lund 1955, Hydrobiologia 7: 225',258,'[212]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(825,'Oscillatoria decolorata','G.S. West 1892, J. Bot. 37: 263',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(826,'Oscillatoria exospira','Skuja 1956, Nova Acta Rec. Soc. Sci. Upsal., Ser. 4, 16(3): 55',258,'[213]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(827,'Oscillatoria granulata','Gardner 1927, <em>Mem. New York Bot. Gard.</em> 7: 37',258,'[215]','','Species',NULL,'','','','freshwater, in pool at the Park, Santurce','[26]',0,1,'',0,'basionym','2019-11-14 14:00:05','admin'),(828,'Oscillatoria griseo-violacea','Skuja 1956, Nova Acta Reg. Soc. Sci. Upsal., Ser. 4, 16(4): 55',258,'[213]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-11-14 14:12:55','admin'),(829,'Oscillatoria ingrica','Voronichin 1931, Acta Horti Bot. Acad. Sci. URSS 44: 225',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(830,'Oscillatoria rhodonema','Skuja 1964, <em>Nova Acta Reg. Soc. Sci. Upsal., Ser. 4,</em> 18(3):: 49',258,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(831,'Oscillatoria exilis var. sequana','Couté 1979, Bull. Mus. Nat. Hist. Natur. Ser. 4, Sec. B, 1: 272',258,'[217]','','Species',NULL,'','','','Matrona Seqaanaque','[59]',0,1,'',0,'basionym','2019-11-15 12:30:04','admin'),(832,'Oscillatoria bornetii f. tenuis','Skuja 1930, Acta Horti Bot. Univ Latv. 10(3): 18',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(833,'Pseudophormidium africanum','(Borge) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:853',0,'active','0000-00-00 00:00:00',NULL),(834,'Pseudophormidium batrachosperma','(Starmach) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:854',0,'active','0000-00-00 00:00:00',NULL),(835,'Pseudophormidium battersii','(Gomont) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'[1043]','','',NULL,NULL,0,1,'clades:866',0,'active','2020-04-22 08:51:39','admin'),(836,'Pseudophormidium edaphicum','(Elenkin) Anagnostidis &amp; Komárek 1988, Algolog. Stud 50-53: 409',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:855',1,'active','2020-04-22 08:48:17','admin'),(837,'Pseudophormidium flexuosum','(Gardner) Anagnostidis &amp; Komárek 1988: 409',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:856',0,'active','0000-00-00 00:00:00',NULL),(838,'Pseudophormidium fortii','(Frémy) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53 409',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:857',0,'active','0000-00-00 00:00:00',NULL),(839,'Pseudophormidium hansgirgii','(Schmidle) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:858',0,'active','0000-00-00 00:00:00',NULL),(840,'Pseudophormidium hollerbachianum','(Elenkin) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:865',0,'active','0000-00-00 00:00:00',NULL),(841,'Pseudophormidium indicum','(Dixit) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:859',0,'active','0000-00-00 00:00:00',NULL),(842,'Pseudophormidium mucicola','(An) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:868',0,'active','0000-00-00 00:00:00',NULL),(843,'Pseudophormidium pauciramosum','(Anissimova) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'[543]','','',NULL,NULL,0,1,'clades:869',0,'active','2019-07-19 12:52:06','admin'),(844,'Pseudophormidium phormidioides','(Hansgirg ex Forti) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:860',0,'active','0000-00-00 00:00:00',NULL),(845,'Pseudophormidium purpureum','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:861',0,'active','0000-00-00 00:00:00',NULL),(846,'Pseudophormidium radiosum','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:862',0,'active','0000-00-00 00:00:00',NULL),(847,'Pseudophormidium rhenanum','(Schmidle) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:870',0,'active','0000-00-00 00:00:00',NULL),(848,'Pseudophormidium spelaeoides','(Čado) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:871',0,'active','0000-00-00 00:00:00',NULL),(849,'Pseudophormidium tatricum','(Starmach) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:872',0,'active','0000-00-00 00:00:00',NULL),(850,'Pseudophormidium tauricum','(Voronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:863',0,'active','0000-00-00 00:00:00',NULL),(851,'Pseudophormidium tenue','(Thuret ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 410',285,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:864',0,'active','0000-00-00 00:00:00',NULL),(852,'Pseudophormidium viride','(Schwabe) Azevedo 1991, Algolog. Stud. 64: 513',285,'[229]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:873',0,'active','0000-00-00 00:00:00',NULL),(853,'Plectonema africanum','Borge 1928, Hedwigia 68: 107',273,'[219]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-05-30 07:13:19',NULL),(854,'Plectonema batrachospermum','Starmach 1957, Acta Soc. Bot. Polon. 26(3): 568',273,'[220]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-05-30 07:19:51',NULL),(855,'Plectonema puteale f. edaphicum','Elenkin 1949, Monogr. Alg. Cyanoph. Pars spec. 2: 1782',273,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:46:54','admin'),(856,'Plectonema flexuosum','Gardner 1927, Mem. N.Y. Bot. Gard. 7: 47',273,'[215]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:14','admin'),(857,'Plectonema fortii','Frémy 1930, Arch. Mot. Mem. 3(2): 171',273,'[221]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:23','admin'),(858,'Plectonema hansgirgii','Schmidle 1900, Hedwigia 39:: 186',273,'[222]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:31','admin'),(859,'Plectonema indicum','Dixit 1936, Proc. Ind. Acad, Sci. 3(1) : 99',273,'[223]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:43','admin'),(860,'Plectonema phormidioides','&nbsp;Hansgirg ex Forti 1907, Syll. Myxoph. p. 493',273,'[436]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:45:28','admin'),(861,'Plectonema purpureum','Gomont 1892, An. Sci. Nat. VII Bot. 16: 101',273,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:45:50','admin'),(862,'Plectonema radiosum','Gomont 1892, An. Sci. Nat. VII Bot, 16: 100',273,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:47:07','admin'),(863,'Plectonema tauricum','Voronichin 1932, &nbsp; &nbsp;313',273,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:48:19','admin'),(864,'Plectonema tenue','Thuret ex Gomont 1892, An. Sci. Nat. VII Bot. 16: 101',273,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:48:26','admin'),(865,'Plectonema boryanum f. hollerbachianum','Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1787',273,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:00','admin'),(866,'Plectonema battersii','Gomont 1899, Bull. Soc. Bot. France 46: 36',273,'[224]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-05-30 07:19:59',NULL),(867,'Plectonema golenkinianum','Gomont 1899, Bull. Soc. Bot. France 46: 35',273,'[224]','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'active','2019-06-07 08:53:39','admin'),(868,'Plectonema mucicola','An 1992, Fragm. Florist. Geobot. 37(2): 410',273,'[225]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:41:53','admin'),(869,'Plectonema purpureum f. pauciramosum','Anissimova in Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1798',273,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:46:01','admin'),(870,'Plectonema rhenanum','Schmidle 1897, Hedwigia 36: 19',273,'[227]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:47:17','admin'),(871,'Plectonema spelaeoides','Čado 1959, : 2',273,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:47:49','admin'),(872,'Plectonema tatricum','Starmach 1963: 431',273,'[228]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:48:01','admin'),(873,'Plectonema polymorphum var, viridis','Schwabe 1960, Oster. Bot. Ztschr. 107(3-4): 291',273,'[230]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-07-31 12:45:42','admin'),(874,'Planktothrix agardhii','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'[1017][1018][1019][1020][1021]','','',NULL,NULL,1,1,'clades:911',0,'active','2020-04-16 12:36:39','admin'),(875,'Planktothrix arnoldii','&nbsp;(Kisselev) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:897',0,'active','2020-04-16 12:42:25','admin'),(876,'Planktothrix clathrata','(Skuja) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:898',0,'active','2020-04-17 05:59:16','admin'),(877,'Planktothrix compressa','(Utermöhl) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'[1022]','','',NULL,NULL,0,1,'clades:899',1,'active','2020-04-17 06:34:37','admin'),(878,'Planktothrix geitleri','(Kisselev) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'[1023]','','',NULL,NULL,0,1,'clades:900',0,'active','2020-04-17 06:38:57','admin'),(879,'Planktothrix mougeotii','(Bory ex Gomont) Anagnostidis &amp; Komárek 1988: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:901',0,'active','2020-04-17 10:59:31','admin'),(880,'Planktothrix planctonica','(Elenkin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:902',0,'active','0000-00-00 00:00:00',NULL),(881,'Planktothrix geitleri','(Kisselev) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(882,'Planktothrix cryptovaginata','(Schkorbatov) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(883,'Planktothrix prolifica','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'[1032]','','',NULL,NULL,0,1,'clades:904',0,'active','2020-04-17 09:47:12','admin'),(884,'Planktothrix perornata','(Skuja) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:903',1,'active','2020-04-17 09:35:25','admin'),(885,'Planktothrix rubescens','(De Candolle ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'[1033][1034][1035][1036][1037][1038][1039][1040][1041]','','',NULL,NULL,0,1,'clades:905',0,'active','2020-04-17 11:05:14','admin'),(886,'Planktothrix zahidii','(Faridi &amp; Khalil) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:907',0,'active','0000-00-00 00:00:00',NULL),(887,'Planktothrix suspensa','(Pringsheim) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:906',0,'active','0000-00-00 00:00:00',NULL),(888,'Planktothrix isothrix','(Skuja) Komárek &amp; Komárková 2004, Czech Phycol. 4: 14',272,'[34]','','Species',NULL,'[1024][1025][1026][1027][1028][1029]','','',NULL,NULL,0,1,'clades:908',0,'active','2020-04-17 07:09:20','admin'),(889,'Planktothrix lacustris','(Klebahn) Umezaki &amp; Watanabe 1994, &nbsp;Jpn. J. Phycol. 42: 199',272,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:909',0,'active','0000-00-00 00:00:00',NULL),(890,'Planktothrix miyadii','(Negoro) Umezaki &amp; Watanabe 1994, Jpn. J. Phycol. 42: 199',272,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:910',0,'active','0000-00-00 00:00:00',NULL),(891,'Planktothrix iwanoffiana','(Nygaard) Umezaki &amp; Watanabe 1994, Jpn. J. Phycol. 42: 199',272,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(892,'Planktothrix raciborskii','(Woloszynska) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 416',272,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:905',1,'active','2020-04-17 10:40:14','admin'),(893,'Planktothrix pseudoagardhii','Suda &amp; Watanabe in Suda et al. 2002, IJSEM 52: 1593',272,'[55]','','Species',NULL,'','','T1-8-4T (= NIES 845T)',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(894,'Planktothrix spiroides','Wang &amp; Li in Liu et al. 2013, Phycologia 52(4): 328',272,'[167]','','Species',NULL,'','HAB2013-0222','Strain fs1','Pond,&nbsp;<br>Guangdong Province','',0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(895,'Oscillatoria raciborskii','Woloszynska 1912, Bull. Internat. Acad, Sci. Cracovie, mat.-nat., Ser. B. 6: 686',258,'[233]','','Species',NULL,'','','','planktic, &nbsp;Rawa Demangan, Java','[157]',0,1,'',0,'active','2019-11-18 13:53:22','admin'),(896,'Oscillatoria agardhii var. isothrix','Skuja 1948: 49',258,'','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(897,'Oscillatoria arnoldii','Kisselev 1927',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(898,'Oscillatoria mougeotiii var. clathrata','Skuja 1956, Nova Acta Reg. Soc. Sci. Upsal. 16(3): 58',258,'[213]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(899,'Lyngbya compressa','Utermöhl 1925, Arch Hydrobiol. Suppl. 5: 285',234,'[234]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(900,'Oscillaria geitleri','Kisselev 1927, Izv. Otd. Prikl. Ichtiol. nauč.-prom. Issled. 5(2): 280',258,'[347]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2020-04-17 06:38:06','admin'),(901,'Oscillatoria mouegotii','Bory ex Gomont 1892, Ann. Sci. Nat. VII. Bot. 16: 230 ???',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(902,'Oscillatoria ornata f. planctonica','Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1265',258,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(903,'Oscillatoria perornata','Skuja 1949, Nova Acta Reg. Soc. Sci. Upsal. Ser. 4, 14(5): 47',258,'','','Species',NULL,'[1030][1031]','','',NULL,NULL,0,1,'',0,'basionym','2020-04-17 09:35:12','admin'),(904,'Oscillatoria prolifica','Gomont 1892, Ann. Sci. Nat. &nbsp;VII, Bot., 16: 205',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(905,'Oscillatoria rubescens','De Candolle ex Gomont 1892, An. Sci. Nat. Bot., ser. VII, &nbsp;16: 204',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(906,'Oscillatoria agardhii var. suspensa','Pringsheim 1965, Arch. Microbiol. 50: 402',258,'[537]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2020-04-17 11:21:47','admin'),(907,'Oscillatoria zahidii','Faridi &amp; Khalil 1974, Biologia (Pakistan) 20(1): 65',258,'[236]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(908,'Oscillatoria agardhii var. isothrix','SKUJA, 1948, &nbsp;Symb. bot. Upsal. 9(3): 49',258,'[238]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(909,'Trichodesmium lacustre','Klebahn 1895, <em>Flora</em> 80: 271',334,'[237]','','Species',NULL,'[710][711]','','',NULL,NULL,0,1,'',0,'basionym','2020-01-09 13:48:58','admin'),(910,'Oscillatoria miyadii','Negoro 1943, Sci. Rep. Tokyo Bunrika Daigaku, Sect. B. No. 94: 80',258,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(911,'Oscillatoria agardhii','Gomont 1892, Ann. Sci Nat. VII Bot, &nbsp;16: 205',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(912,'Planktothrix iwanoffiana','(Nygaard) Umezaki et Watanabe 1994, Jpn. J. Phycol. 42: 199',272,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:913',1,'active','2020-01-09 12:50:19','admin'),(913,'Trichodesmium iwanoffianaum','Nygaard 1926, Vidensk. Medd. Dansk Naturh. Foren. 82: 21',334,'[239]','','Species',NULL,'[708][709]','','','freshwater; Sumatra – Lake Toba','[157]',0,1,'clades:891',0,'basionym','2020-01-09 12:53:31','admin'),(914,'Anabaena fuellebornii','Schmidle ????',102,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(915,'Anabaena mysorensis','Gonzalves et Kamat 1959, Hydrobiologia 13: 237',102,'[240]','','Species',NULL,'','personal collection of Gonzalves No M. 12','','attached to grass in a puddle, Devarayi, Mysore State','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(916,'Anabaena unispora','Gardner 1927, Mem N.Y. Bot. Garden 7: 59',102,'[215]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(917,'Anabaena volzii','Lemmermann 1906, &nbsp;Abh. Nat. Ver. Bremen 18(1): 153',102,'[242]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(918,'Anabaena alatospora','Gonzalves et Kamat 1959, Hydrobiologia 13(3): 236',102,'[240]','','Species',NULL,'','personal collection of Gonzalves No M.11','','mucilaginous mass in a puddle, Devarayi, Mysore State','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(919,'Nostoc muscorum','Agardh ex Bornet et Flahault 1888, Ann. Sc. Nat. 7th Ser: 7:200',255,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(920,'Cyanocohniella calida','Kaštovský, Berrendero, Hladil et Johansen 2014, Phytotaxa 181(5): &nbsp;282',709,'[195]','','Species',NULL,'','CBFS A-023','CCALA 1049','Thermal mineral water and atmophytic localities around thermal springs, Karlovy Vary','',1,1,'',0,'active','2020-08-24 08:23:47','admin'),(921,'Anabaena siamensis','Antarikanonda 1985, Nova Hedwigia 41: 345',102,'[243]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(922,'Cylindrospermum planctonicum','Cronberg 2003, Algolog. Stud. 109: 205',166,'[244]','','Species',NULL,'','','','plankton of the brackish water bays of Osthammarsfjärden','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(923,'Dolichospermum flos-aquae','([Lyngbye] Brébisson ex Bornet et Flahault) &nbsp;Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 60',172,'[60]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:924',0,'active','0000-00-00 00:00:00',NULL),(924,'Anabaena flos-aquae','[Lyngb ye] Brébisson ex Bornet et Flahault 1888, Ann. Sci. Nat. Bot. VII, 7: 228',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(925,'Dolichospermum affinine','(Lemmermann) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:926',0,'active','2019-12-12 06:04:17','admin'),(926,'Anabaena affinis','&nbsp;Lemmermann 1898, Abh. Naturw. Ver. Bremen 14: 261',102,'[245]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(927,'Dolichospermum akankoensis','(M. Watanabe) Wackli, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:928',0,'active','0000-00-00 00:00:00',NULL),(928,'Anabaena akankoensis','M. Watanabe 2003, Bull. Natn. Sci. Mus.,Tokyo, Ser. B, 29: 9–13',102,'[246]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(929,'Anabaena arctica','Kiselev 1932, Gosud. Hidrol. Inst., Issled. Morej SSSR 15: 98',102,'[247]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(930,'Dolichospermum arcticum','(Kiselev) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:929',0,'active','0000-00-00 00:00:00',NULL),(931,'Anabaena bituri','Cronberg et Komárek 2004, Nova Hedwigia 78: 75',102,'[248]','','Species',NULL,'','A2055','','planktic, small reservoirs in the vicinity of Lake Kariba','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(932,'Dolichospermum bituri','(Cronberg et Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:931',0,'active','0000-00-00 00:00:00',NULL),(933,'Anabaena berezowskii','Usačev 1928, Tr. Sibir. Naučn. Ribochoz. Stan. Krasnojarsk 3(2): 32',102,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(934,'Dolichospermum berezowskii','(Usačev) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:933',0,'active','0000-00-00 00:00:00',NULL),(935,'Anabaena bothai','Welsh 1961, Rev. de Biol. 2(3/4): 259–260',102,'[249]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(936,'Dolichospermum bothai','(Welsh) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:935',0,'active','0000-00-00 00:00:00',NULL),(937,'Anabaena caspica','Ostenfeld 1902, Vidensk. Medd. Naturh. Fören. Kjøbenhavn 1901: 138',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(938,'Dolichospermum caspicum','&nbsp;(Ostenfeld) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:937',0,'active','0000-00-00 00:00:00',NULL),(939,'Anabaena circinalis','Rabenhorst ex Bornet et Flahault 1988, Ann. Sci. Nat. 7, Bot 7: 230',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(940,'Dolichospermum circinalis','(Rabenhorst ex Bornet et Flahault) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:939',0,'active','0000-00-00 00:00:00',NULL),(941,'Anabaena citrispora','M. Watanabe 1992, Bull. Nat. Sci. Mus., ser. B, 18(4): 124–126',102,'[250]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(942,'Dolichospermum citrisporum','(M. Watanabe) Wacklin, Hoffmann et Komárek 2009, Fottes 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:941',0,'active','0000-00-00 00:00:00',NULL),(943,'Anabaena spiroides var. minima f. compacta','Nygaard 1949, &nbsp;Kong. Danske Vidensk. Selsk., Biol. Skr. 7(1): 205',102,'[251]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(944,'Dolichospermum compactum','(Nygaard) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'[246]','','',NULL,NULL,0,1,'clades:943',0,'active','0000-00-00 00:00:00',NULL),(945,'Anabaena spiroides var. crassa','Lemmermann 1898, &nbsp;Bot. Centralbl. 76(5-6): 155',102,'[252]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(946,'Dolichospermum crassum','(Lemmermann) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'[247]','','',NULL,NULL,0,1,'clades:945',0,'active','0000-00-00 00:00:00',NULL),(947,'Anabaena curva','&nbsp;Hill 1976, &nbsp;Phycologia 15(1): 62',102,'[253]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(948,'Dolichospermum curvum','(Hill) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:947',0,'active','0000-00-00 00:00:00',NULL),(949,'Anabaena viguieri var. danica','Nygaard 1949, Kong. Danske Vidensk. Selsk., Biol. Skr. 7(1): 212',102,'[251]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(950,'Dolichospermum danicum','(Nygaard) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'[248]','','',NULL,NULL,0,1,'clades:949',0,'active','0000-00-00 00:00:00',NULL),(951,'Anabaena delicatula','Lemmermann 1898, Bot. Centralbl. 76: 155',102,'[252]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(952,'Dolichospermum delicatulum','(Lemmermann) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:951',0,'active','0000-00-00 00:00:00',NULL),(953,'Anabaena ellipsoides','Bolochoncev ex Woronichin 1931, Tr. Bot. Sada AN SSSR 44: 221',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(954,'Dolichospermum ellipsoides','(Bolochoncev ex Voronichin) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:953',0,'active','0000-00-00 00:00:00',NULL),(955,'Anabaena fallax','Komárek et Komárková-Legnerová 2002, Preslia 74: 223',102,'[254]','','Species',NULL,'','','','planktic, Chapultepec Park, Mexico City','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(956,'Dolichospermum fallax','(Komárek et Komárková- Legnerová) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:955',0,'active','0000-00-00 00:00:00',NULL),(957,'Anabaena farciminiformis','Cronberg et Komárková-Legnerová 1988, Algolog. Stud. 50– 53: 278',102,'[255]','','Species',NULL,'','','','planktic; O. Grevie, Scania','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(958,'Dolichospermum farciminiformis','(Cronberg et Komárková-Legnerová) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:957',0,'active','0000-00-00 00:00:00',NULL),(959,'Anabaena fusca','Hill 1976, Phycologia 15(1): 70',102,'[253]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(960,'Dolichospermum fusca','(Hill) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:959',0,'active','0000-00-00 00:00:00',NULL),(961,'Anabaena halbfassii','Bachmann, Ber. Dtsch. Bot. Ges. 31: 187, 1913',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(962,'Dolichospermum halbfassii','(Bachmann) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:961',0,'active','0000-00-00 00:00:00',NULL),(963,'Anabaena helicoidea','Bernard 1908, Protococc. &amp; Desmid. d’Eau Douce, p. 52',102,'[256]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(964,'Dolichospermum helicoideum','(Bernard) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:963',0,'active','0000-00-00 00:00:00',NULL),(965,'Anabaena heterospora','Nygaard 1949 Kong. Danske Vidensk. Selsk., Biol. Skr., 7(1): 195',102,'[251]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(966,'Dolichospermum heterosporum','(Nygaard) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 61-62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:965',0,'active','0000-00-00 00:00:00',NULL),(967,'Anabaena jacutica','Kiselev 1932, Gosud. Hidrol. Inst., Issled. Morej SSSR 15: 100',102,'[247]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(968,'Dolichospermum jacuticum','(Kiselev) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:967',0,'active','0000-00-00 00:00:00',NULL),(969,'Anabaena lemmermannii','Richter in Lemmermann 1903, Forschungsber. Biol. Stat. Plön 10: 153',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(970,'Dolichospermum lemmermannii','(Richter in Lemmermann) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:969',0,'active','0000-00-00 00:00:00',NULL),(971,'Anabaena spiroides var. longicellularis','Pankow 1965, Limnologova &nbsp;3(2): 163–172, 1965',102,'[257]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(972,'Dolichospermum longicellularis','(Pankow) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'[249]','','',NULL,NULL,0,1,'clades:971',0,'active','0000-00-00 00:00:00',NULL),(973,'Anabaena macrospora','&nbsp;Klebahn 1895, Flora 80: 269',102,'[237]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(974,'Dolichospermum macrosporum','(Klebahn) &nbsp;Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(975,'Anabaena maxima','Cronberg et Komárek 2004, Nova Hedwigia 78(1/2): 77',102,'[248]','','Species',NULL,'','A 2058','','Planktic in large lakes','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(976,'Dolichospermum maximum','(Cronberg et Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:975',0,'active','0000-00-00 00:00:00',NULL),(977,'Dolichospermum maximum','(Cronberg et Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(978,'Anabaena mendotae','Trelease 1889, Trans. Wisconsin Acad. Sci. 7: 123',102,'[258]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(979,'Dolichospermum mendotae','(Trelease) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:978',0,'active','0000-00-00 00:00:00',NULL),(980,'Anabaena mucosa','Komárková-Legnerová et Eloranta 1992, Algolog. Stud. 67: 125–126',102,'[259]','','Species',NULL,'','','','freshwater, lake Keitele, Suolahti bay','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(981,'Dolichospermum mucosum','(Komárková-Legnerová et Eloranta) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:980',0,'active','0000-00-00 00:00:00',NULL),(982,'Anabaena nathii','Vasishta 1960, Res. Bull. (N.S.) Panjab Univ., 11(I–II): 67',102,'[260]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(983,'Dolichospermum nathii','(Vasishta) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:982',0,'active','0000-00-00 00:00:00',NULL),(984,'Anabaena nygaardii','Cronberg et Komárek 2004, Nova Hedwigia 78: 77– 78',102,'[248]','','Species',NULL,'','','','planktic, eutrophic water, lake Kariba','',0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(985,'Dolichospermum nygaardii','(Cronberg et Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:984',0,'active','0000-00-00 00:00:00',NULL),(986,'Anabaena perturbata','Hill 1976, Phycologia 15(1): 67',102,'[261]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(987,'Dolichospermum perturbatum','(Hill) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:986',0,'active','0000-00-00 00:00:00',NULL),(988,'Anabaena planctonica','Brunnthaler, Sitzungsb. K. Akad. Wiss. Wien, mat.–nat., 112: 292, 1903',102,'[262]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(989,'Dolichospermum planctonicum','(Brunnthaler) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:988',0,'active','0000-00-00 00:00:00',NULL),(990,'Anabaena pseudocompacta','M. Watanabe 1996, Bull. Nat. Sci. Museum, Ser. B, 22(3): 94',102,'[263]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(991,'Dolichospermum pseudocompactum','(M. Watanabe) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:990',0,'active','0000-00-00 00:00:00',NULL),(992,'Anabaena sigmoidea','Nygaard 1949 Kong. Danske Vidensk. Selsk. Biol. Skr. 7(1): 199',102,'[251]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(993,'Dolichospermum sigmoideum','(Nygaard) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:992',0,'active','0000-00-00 00:00:00',NULL),(994,'Anabaena skujae-laxa','Komárek et Zapomělová 2007, Fottea 7(1): 27',102,'[36]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(995,'Dolichospermum skujae-laxum','(Komárek et Zapomělová) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'[250]','','',NULL,NULL,0,1,'clades:994',0,'active','0000-00-00 00:00:00',NULL),(996,'Anabaena solitaria f. smithii','Komárek &nbsp;in Komárek &amp; Ettl 1958, Algolog. Studien p. 129',102,'[264]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(997,'Dolichospermum smithii','(Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'[251]','','',NULL,NULL,0,1,'clades:996',0,'active','0000-00-00 00:00:00',NULL),(998,'Anabaena solitaria','Klebahn 1895, &nbsp;Flora 80: 270',102,'[237]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(999,'Dolichospermum solitarium','(Klebahn) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:998',0,'active','0000-00-00 00:00:00',NULL),(1000,'Anabaena spiroides','Klebahn 1895, Flora 80: 268',102,'[237]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1001,'Dolichospermum spiroides','(Klebahn) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1000',0,'active','0000-00-00 00:00:00',NULL),(1002,'Anabaena torques-reginae','Komárek 1984, Acta Bot. Cubana 19: 14–16',102,'[265]','','Species',NULL,'','','','Boca de Laguna del Tesoro in peninsula Zapata','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1003,'Dolichospermum torques-reginae','(Komárek) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1002',0,'active','0000-00-00 00:00:00',NULL),(1004,'Anabaena viguieri','Denis et Frémy 1924, Bull. Soc. Linn. Normandie, Ser. 7, 6: 122',102,'[266]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1005,'Dolichospermum viguieri','(Denis et Frémy) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1004',0,'active','0000-00-00 00:00:00',NULL),(1006,'Anabaena werneri','Brunnthaler 1903, Sitzungsb. K. Akad. Wiss. Wien, mat.–nat., 112(1): 292',102,'[262]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1007,'Dolichospermum werneri','(Brunnthaler) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1006',0,'active','0000-00-00 00:00:00',NULL),(1008,'Anabaena zinserlingii','Kosinskaja 1929, Russ. Arch. Protistol. 8(3/4): 245, 248',102,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1009,'Dolichospermum zinserlingii','(Kosinskaja) Wacklin, Hoffmann et Komárek 2009, Fottea 9(1): 62',172,'[60]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1008',0,'active','0000-00-00 00:00:00',NULL),(1010,'Anathece clathrata','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','M10D5',NULL,NULL,1,1,'clades:1022',0,'active','0000-00-00 00:00:00',NULL),(1011,'Anathece minutissima','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1024',0,'active','0000-00-00 00:00:00',NULL),(1012,'Anathece stratus','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1026',0,'active','0000-00-00 00:00:00',NULL),(1013,'Anathece bachmannii','Komárek, Kaštovský et Jezberová 2011.<em>&nbsp;European Journal of Phycology 46(3):322</em>',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1027',0,'active','0000-00-00 00:00:00',NULL),(1014,'Anathece bacteriosa','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1028',0,'active','0000-00-00 00:00:00',NULL),(1015,'Anathece endophytica','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1016,'Anathece smithii','Komárek, Kaštovský et Jezberová 2011. European Journal of Phycology 46(3): 322',394,'[75]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1029',0,'active','0000-00-00 00:00:00',NULL),(1017,'Epigloeosphaera glebulenta (Zalessky)','Komárková=Legnerová J. 1991. Algological STudies 62: 11',176,'[80]','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1018,'Epigloeosphaera filamentosa','Komárek et Cronberg 2001. Nova Hedwigia 73(1-2): 134',176,'[267]','holotypus (icona typica): figura nostra 2a, e','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1019,'Epigloeosphaera brasilica','Azevedo, Sant\'Anna, Senna, Komárek &amp; Komárková 2003. Hoehnea 20: 286',176,'[268]','','Species',NULL,'','SP 355737','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1020,'Cyanocatenula calyptrata','Joosten 2006. Flora of the blue-green algae of the Netherlands, p. 34, 207',148,'[24]','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1021,'Cyanoaggregatum brasiliense','Werner, &nbsp;Sant\'Anna, et &nbsp;Azevedo, 2008. Revista Brasileira de Botanica 31(3): 494',675,'[61]','','Species',NULL,'','HAS 6897','HAS 6897',NULL,NULL,1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1022,'Aphanothece clathrata','W. West in W. et G.S.West 1906. Trans. Roy, Irish Acad. 33(A): 111',106,'[269]','','Species',NULL,'','','','','[67]',0,1,'',0,'basionym','2019-04-16 02:48:00','admin'),(1023,'Aerosakkonema','Thu et Watanabe 2012. Phycologia 51(6): 675',2553,'[270]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:27:51','admin'),(1024,'Microcystis minutissima','W.West 1912. Proc. Royal. Irish Acad. 31(16): 1-62',247,'[271]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1025,'Aphanothece minutissima','(W.West) Komárková-Legnerová et Cronberg 1994. Algolog. Stud. 72: 24',106,'[272]','','Species',NULL,'','','','','[90]',0,1,'',0,'active','2019-04-16 02:47:40','admin'),(1026,'Aphanothece stratus','Komárek et Cronberg 2001, Nova Hedwigia 73(1-2): 133',106,'[267]','','Species',NULL,'','','','','[228]',0,1,NULL,0,'basionym','2019-04-16 02:47:03','admin'),(1027,'Aphanothece bachmannii','Komárková-Legenerová et Crongberg 1994. Algolog. Stud. 72: 21',106,'[272]','','Species',NULL,'','','','','[90]',0,1,NULL,0,'basionym','2019-04-16 02:48:24','admin'),(1028,'Aphanothece bacteriosa','Komárek et Komárková-Legnerová 2007. Nova Hedwigia 84(1-2): 72',106,'[35]','','Species',NULL,'','','','','[95]',0,1,NULL,0,'basionym','2019-04-16 02:48:39','admin'),(1029,'Aphanothece smithii','Komárková-Legnerová et Cronberg 1994. Algolog. Stud. 72: 25',106,'[272]','','Species',NULL,'','','','','[90]',0,1,NULL,0,'basionym','2019-04-16 02:47:28','admin'),(1030,'Albertania','Zammit 2018. Phycologia 57(5): &nbsp;483',1034,'[273]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:17:33','admin'),(1031,'Albertania skiophila','Zammit 2018. Phycologia 57(5): 483',1030,'[273]','','Species',NULL,'','CY21176','SA373/Zammit 2014','subaerophytic on limestone in catacombs','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1032,'Albertania','Zammit 2018. Phycologia 57(5): 483',61,'[273]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1033,'Albertania skiophila','Zammit 2018. Phycologia 57(5): 483',61,'[273]','','Species',NULL,'','CY21176','SA373/Zammit 2014','catacomb sites in Rabat','',1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1034,'Oculatellaceae','Mai et Johansen in Mai et al. 2018. <em>Phytotaxa</em> 365(1): 17',2547,'[274]','','Family',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:16:38','admin'),(1035,'Pegethrix','Mai, Johansen et Bohunická in Mai et al. 2018. Phytotaxa 365(1): 17',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1036,'Pegethrix bostrychoides','Mai, J.R.Johansen &amp; Bohunická 2018. Phytotaxa 365(1): 17',1035,'[274]','','Species',NULL,'','BRY37770','GSE-PSE-MK47-15B','Sandstone seep wall with small moist area and larger pond below the rock face, within Strait Cliffs Formation, in the GSENM, Kane County, Utah,','',1,1,NULL,0,'active','2021-05-07 11:24:05','admin'),(1037,'Pegethrix olivacea','Mai, J.R.Johansen &amp; Bohunická 2018. Phytotaxa 365(1): 22',1035,'[274]','','Species',NULL,'','BRY37772!','GSE-PSE-MK46-15A','Sandstone seep wall with small moist area and larger pond below the rock face, within Strait Cliffs Formation, in the GSENM, Kane County, Utah','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1038,'Pegethrix convoluta','Mai, Johansen &amp; Bohunická 2018. Phytotaxa 365(1): 22',1035,'[274]','','Species',NULL,'','BRY37773!','GSE-PSE-MK38-07D','Lower Calf Creek Falls site, Grand Staircase-Escalante National Monument, large seep wall and waterfall in Navajo Sandstone, in the GSENM, Kane County, Utah,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1039,'Pegethrix indistincta','Mai, Johansen &amp; Bohunická 2018. Phytotaxa 365(1): 24',1035,'[274]','','Species',NULL,'','BRY 37774!, BRY37775!, BRY37776!','GSE-TBC-7GA','Lower Calf Creek Falls site, Grand Staircase-Escalante National Monument, large seep wall and waterfall in Navajo Sandstone, in GSENM, Kane County, Utah,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1040,'Drouetiella','Mai, Johansen et Pietrasiak 2018, Phytotaxa 365(1): 27',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1041,'Drouetiella lurida','(Gomont) Mai, J.R.Johansen &amp; Pietrasiak 2018, Phytotaxa 365(1): 28',1040,'[274]','','Species',NULL,'[486]','Epitype BRY37777','Lukesova 1986/6,','tailings of Cainozoic clay','[54]',1,1,'clades:1042',0,'active','2021-05-07 11:33:09','admin'),(1042,'Phormidium luridum','Gomont 1892, Annales des Sciences Naturelles, ser. 7 16:165',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1043,'Leptolyngbya lurida (Gomont)','Anagnostidis &amp; Komárek 1988. Algolog. Stud. 80: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-05-31 10:39:02',NULL),(1044,'Drouetiella fasciculata','Mai, Johansen et Bohunická 2018. Phytotaxa 365(1): 32',1040,'[274]','','Species',NULL,'','BRY37779!','GSE-PSE-MK29-07A','Lower Calf Creek Falls site, in the Grand Staircase-Escalante National Monument, Large seep wall and waterfall in Navajo Sandstone, found in mats with filamentous algae, in the GSENM, Kane County, Utah,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1045,'Drouetiella hepatica','Mai, Johansen et Pietrasiak 2018. Phytotaxa 365(1): 33',1040,'[274]','','Species',NULL,'','BRY37778!','UHER 2000/2452','&nbsp;National Park Slovak Paradise: Waterfall Kaskady, gorge Sucha Bela','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1046,'Timaviella obliquedivisa','Mai, Johansen et Bohunická 2018. Phytotaxa 365(1): 34',630,'[274]','','Species',NULL,'','BRY37787!, BRY37788!','GSE-PSE-MK28-08A','Big Horn Seep Wall, Grand Staircase-Escalante National Monument, Hanging garden (concave wet rock face in a grotto with vascular plants hanging from the rock) on a sandstone rock wall in the Carmel-Page formation, partly covered with organic debris, mosse','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1047,'Timaviella radians','Mai, Johansen &amp; Bohunická 2018. Phytotax 365(1): : 36',630,'[274]','','Species',NULL,'','BRY37789!','GSE-UNK-7R','Lower Calf Creek Falls site, Grand Staircase-Escalante National Monument, Large seep wall and waterfall in Navajo Sandstone, in the GSENM, Kane County, Utah.&nbsp; Mats in waterfall.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1048,'Cartusia','Mai, Johansen et Pietrasiak 2018. Phytotaxa 365(1): 38',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1049,'Cartusia fontana','(Hansgirg) Mai, Johansen et Pietrasiak 2018. Phytotaxa 365(1): 38',1048,'','','Species',NULL,'[233]','Epitype BRY37780','Kovacik 1999/1',NULL,NULL,1,1,'Lyngbya fontana',0,'active','2019-06-05 11:58:20','admin'),(1050,'Lyngbya fontana','Hansgirg 1892. Archiv für die naturwissenschaftliche Landesdurchforschung von Böhmen 8: 85',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,0,'',1,'active','2019-06-05 11:58:20','admin'),(1051,'Tildeniella','Mai, J.R.Johansen &amp; Bohunická 2018. Phytotaxa 365(1): 40',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1052,'Tildeniella torsiva','Mai, Johansen &amp; Pietrasiak 2018. Phytotaxa 365(1): 40',1051,'[274]','','Species',NULL,'','BRY37781!','Uher 1998/13d','National Park Slovak Paradise: Gorge Prielom Hornadu, found in limestone wall near tourist walkway','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1053,'Tildeniella nuda','Mai, Johansen &amp; Bohunická 2018, Phytotaxa 365(1): 42',1051,'[274]','','Species',NULL,'','BRY37782!','Zehnder 1965/U140,','Stansstaad, &nbsp;found on a wet stone wall','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1054,'Komarkovaea','Mai, Johansen &amp; Pietrasiak 2018. Phytotaxa 365(1): 44',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1055,'Komarkovaea angustata','Mai, Johansen et Pietrasiak 2018. Phytotaxa 365(1): 44',1054,'[274]','','Species',NULL,'','BRY37783','EY1-AM2','&nbsp;El Yunque National Forest: Waterfall in the forest','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1056,'Kaiparowitsia','Mai, Johansen &amp; Bohunická, 2018. Phytotaxa 365(1): 46',1034,'[274]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1057,'Kaiparowitsia implicata','Mai, Johansen et Bohunická 2018. Phytotaxa 365(1): &nbsp;46',1056,'[274]','','Species',NULL,'','BRY37784','GSE-PSE-MK54-09C','Utah, Camp Spring Site 1, Grand Staircase-Escalante National Monument','',1,1,NULL,0,'active','2019-07-10 07:37:29','admin'),(1058,'Chroakolemma','Becerra-Absalon et Johansen 2018',61,'[276]','','Genus',NULL,'','','',NULL,NULL,0,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(1059,'Chroakolemma opaca','Becerra-Absalón et Johansen 2018. Phytotaxa 367(3): 204',61,'[276]','','Species',NULL,'','FCME CB18!,','UNAM 701',NULL,NULL,1,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1060,'Chroakolemma pellucida','Becerra-Absalón et Johansen 2018. <em>Phytotaxa</em> 367(3):&nbsp; 204',61,'[276]','','Species',NULL,'','FCME CB1!','UNAM 719',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1061,'Chroakolemma','Becerra-Absalón et Johansen 2018. <em>Phytotaxa</em> 367(3): &nbsp;201-218',61,'[276]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1062,'Chroakolemma opaca','Becerra-Absalón et Johansen 2018. <em>Phytotaxa</em> 367(3): &nbsp;204',1061,'','','Species',NULL,'','FCME CB18','UNAM 701','Aerophytic, forming surface biocrust with other species from semi-desert soils, Ampliación La Peña, in Mezquital Valley, Hidalgo','[100]',1,1,'',0,'active','2021-06-18 11:01:45','admin'),(1063,'Chroakolemma pellucida','Becerra-Absalón et Johansen 2018. <em>Phytotaxa</em> 367(3): &nbsp;204',1061,'[276]','','Species',NULL,'','FCME CB1!','UNAM 719','Aerophytic, in biocrusts with other species from semi-desert soils, Outside of the cone of the volcanic lake, Atexcac, Puebla','[100]',0,1,NULL,0,'active','2021-06-18 11:02:26','admin'),(1064,'Chroakolemma edaphica','(Elenkin) Becerra-Absalón et Johansen 2018. <em>Phytotaxa</em> 367(3): &nbsp;207',1061,'[276]','','Species',NULL,'[234][235][1042][1044]','','',NULL,NULL,0,1,'clades:855',0,'active','2020-04-22 08:53:20','admin'),(1065,'Leptolyngbya edaphica (Elenkin)','Anagnostidis et Komárek in Anagnostidis 2001. Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,0,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1066,'Geitleriaceae','Kilgore et Johansen 2018. Fottea 18(2): 159',9,'[277]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-06-11 05:52:59','admin'),(1067,'Geitleria appalachiana','Kilgore et Johansen 2018. Fottea 18(2): 159',184,'[277]','','Species',NULL,'','BRY37793','','wall in a cave with light present','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1068,'Trichocoleusaceae','T.Mai et J.R.Johansen 2018. Notulae algarum 72:2',2548,'[278][274]','','Family',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:36:06','admin'),(1069,'Pantanalinema','Vaz et al., 2015. IJSEM 65: 301',61,'[100]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1070,'Pantanalinema rosaneae','Vaz et al. 2015',1069,'[100]','','Species',NULL,'','SP428.663','CENA516','water samples collected from Salina Verde in the Pantanal wetlands, Mato Grosso do Sul<br>State','',1,1,'',0,'active','2019-12-05 13:01:25','admin'),(1071,'Alkalinema pantanalense','Vaz et al. 2015. IJSEM 65: 305',432,'[100]','','Species',NULL,'','SP428.668','CENA528','water samples collected from Salina Preta in the Pantanal wetlands, Mato Grosso do Sul State','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1072,'Amphiheterocytum','Sant Anna et al. 2019. Algal Research 37: 212',25,'[279]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1073,'Amphiheterocytum lacustre','Sant Anna et al. 2019. Algal Research 37: 212',1072,'[279]','','Species',NULL,'','SP 469314','CCIBt 3622','Free floating in freshwater tropical eutrophic lakes, Amanari Lake, &nbsp;Ceará<br>State','[172]',1,1,'',0,'active','2021-07-28 05:15:29','admin'),(1074,'Oscillatoria pseudacutissima','Geitler 1956. Österr. Bot. Zeitschr. 103(2–3): 343',258,'[280]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1075,'Oscillatoria amphibia','Agardh ex Gomont, 1892. Ann. Sci. Nat.–Bot. 16: 221',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1076,'Oscillatoria acutissima','Kufferath, 1914. Ann. Biol. Lac. 7: 264',258,'[281]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1077,'Oscillatoria carotinosa','Geitler, 1956. Österr. Bot. Zeitschr. 103(2–3): 342',258,'[280]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1078,'Oscillatoria deflexa','W. et G.S. West, 1911. Brit. Antarct. Exped. 1(7): 295',258,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,1,'basionym','0000-00-00 00:00:00',NULL),(1079,'Oscillatoria deflexa','W. et G.S. West, Brit. Antarct. Exped. 1(7): 295',258,'[282]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1080,'Geitlerinema epiphloeophyticum','Anagnostidis, 2001. Preslia 73: 364',186,'[9]','icona typica Brühl &amp; Biswas 1923, J. Dept. Sci. Calcutta Univ. 4: 3, pl. 1 5a-b, figura nostra 8','Species',NULL,'','','','Subaerophytic, epiphytic','',0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1081,'Oscillatoria exilis','&nbsp;Skuja, 1964. N. Acta Reg. Soc. Sci. Upsal. Ser. 4, 18(3): 51',258,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1082,'Oscillatoria ionica','Skuja, 1937. Hedwigia 77: 30',258,'[283]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1083,'Oscillatoria lacus–solaris','Campbell et Golubic, 1985. Algol. Stud. 38/39: 324–325',258,'[284]','','Species',NULL,'','','CAMPBELL/OSLSSL 7803801','benthic mats of Solar Lake','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1084,'Oscillatoria lemmermannii','Woloszynska, 1912. Bull. Int. Acad. Sci. Cracovie, mat.–nat., Ser. B, 1913: 687',258,'[233]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1085,'Oscillatoria amphibia f. tenuis','Anisimova in Elenkin, 1949. Monographia algarum 2: 1326',258,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1086,'Caldora','Engene et al. 2015, J. Phycol. 51: 678',44,'[286]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:32:19','admin'),(1087,'Caldora penicillata','(Gomont) Engene, Tronholm et Paul, J. Phycol. 51: 679',1086,'[286]','','Species',NULL,'[245]','','','epizoic on corals and epilithic, Looe Key, Florida','',1,1,'clades:1088',0,'active','0000-00-00 00:00:00',NULL),(1088,'Phormidium penicillatum','Gomont, 1893. Bulletin de la Société Botanique de France 40: 159',267,'[287]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1089,'Cephalothrix','Da Silva Malone, Rigonato, Laughinghouse, Schmidt, Bouzon, Wilmotte, Fiore &amp; &nbsp;Sant\'Anna, 2015. IJSEM 65: 3003',2553,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:28:33','admin'),(1090,'Cephalothrix komarekiana','Malone et al, 2015. IJSEM 65: 3003',1089,'[288]','','Species',NULL,'','SP427.779','CCIBt 3277','grows in an alkaline lake in the Brazilian Pantanal wetlands','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1091,'Cephalothrix lacustris','Malone et al., 2015. IJSEM 65: 3004',1089,'[288]','','Species',NULL,'','SP 428.686','CCIBt 3261','grows in a freshwater lake in the Botanical Garden','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1092,'Jacksonvillea','Hašler, Casamatta, Dvořák et Poulíčková 2017, Phycologia 56(3): 289',46,'[289]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1093,'Jacksonvillea apiculata','Hašler, Casamatta, Dvořák et Poulíčková, 2017. Phycologia 56(3): 291',1092,'[289]','ISOTYPE: OLM Botany 24: Lichens and others no. 9221, strain UPOC 58/2013,','Species',NULL,'','OLM Botany 24: Lichens and others no. 9220','UPOC 77b/2013','epipsamic, on fine sandy sediment with low portion of organic detritus, Lake Oneida, &nbsp;Jacksonville, Florida,','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1094,'Halotia','Genuarion et al., &nbsp;2015. IJSEM 65(2): 667',34,'[295]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1095,'Halotia branconii','Genuário et al, 2015. IJSEM 65(2): 667-670',1094,'[295]','Etymology: Halotia branconii &nbsp;named for L. H. Z. Branco, a Brazilian taxonomist of cyanobacteria','Species',NULL,'','SP 428496','CENA392','on bones in Antarctica and mangrove soils in Brazil','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1096,'Halotia longispora','Genuário et al. 2015, IJSEM 65(2): 670',1094,'[295]','','Species',NULL,'','SP 428499)','CENA420','in mangrove soil in Brazil and in Antarctica (close to the Baranowski glacier)','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1097,'Halotia werneriae','Genuário et al. 2015, IJSEM 65(2): 671',1094,'[295]','','Species',NULL,'','SP 428501','CENA158','in mangrove soil in Brazil and on bones in Antarctica','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1098,'Oscillatoria constricta','Szafer, 1910. Bull. Int. Acad. Sci. Cracovie, Mat-Nat Sci, ser. B: 164',258,'[297]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1099,'Lightfootiella','&nbsp;(Lightfoot) Hašler, Pentecost, Jahodářová, Dvořák &amp; Poulíčková, 2018. Phytotaxa 362 (2): 177',23,'','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:47:23','admin'),(1100,'Lightfootiella montana','(Lightfoot) Hašler, Pentecost, Jahodářova, Dvořák &amp; Poulíčková 2018: 177',1099,'[298]','Basionym: Ulva montana Lightfoot 1777','Species',NULL,'[256][257][258][261][262][263][259]','','','aerophytic to subaerophytic, on quartzite or granitic stones, sometimes among mosses, in mountains','',1,1,'',0,'active','2021-06-18 08:26:49','admin'),(1101,'Oscillatoria princeps','Vaucher ex Gomont',258,'[304][235][317]','','Species',NULL,'','CBFS A-89-1 (epitype)','CCALA 1115','benthos of lakes','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1102,'Limnolyngbya','Li et Li, 2016, Phycologia 55(4): 479',61,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1103,'Limnolyngbya circumcreta','(G.S.West) X.Li &amp; R.Li. 2016, Phycologia 55(4): 480',1102,'[306]','','Species',NULL,'[264]','HAB2014-0112 - neotype','CHAB 5683','Pond, lake, and reservoir','',1,1,'clades:1104',0,'active','0000-00-00 00:00:00',NULL),(1104,'Lyngbya circumcreta','G.S.West, 1907. Journal of the Linnaean Society of London, Botany 38: 174',234,'[307]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1105,'Nunduva','González–Resendiz, León–Tejera et Johansen in González–Resendiz et al., 2018, Fottea 18(1): 88',36,'[308]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1106,'Nunduva fasciculata','González–Resendiz, León–Tejera et Johansen in González–Resendiz et al., 2018, Fottea 18(1): 88',1105,'[308]','Isotypes: FCME–C57, FCME–C58, Paratypes: FCME–C36, –C645, –C719, –C737, –C1313,<br>–C1288, –C1289 and –C1290','Species',NULL,'','FCME–C694','FCME C694–M8–K148','Supratidal and intertidal fringe; epilithic on granitic rock; Oaxaca: San Agustín Bay','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1107,'Nunduva kania','González–Resendiz, León–Tejera et Johansen in González–Resendiz et al., 2018, Fottea 18(1): 89',1105,'[308]','','Species',NULL,'','UNAM C458–M16–K66','FCME C458–M16–K66','Intertidal fringe; epilithic on basaltic rock; Veracruz: Playa Hermosa','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1108,'Limnospira','Nowicka-Krawczyk, Mühlsteinová et Hauer 2019. Scientific Reports 9: 694, p. 3',2413,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-01-14 13:16:32','admin'),(1109,'Spirulina fusiformis','Voronichin 1934. Trudy Soveta Izucheniu Prirodnych Resursov, Ser. Sibirsk. 8: 182',316,'[310]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','2019-08-05 05:49:59','admin'),(1110,'Limnospira fusiformis','(Voronichin) Nowicka-Krawczyk, Mühlsteinová et Hauer 2019. Scientific Reports 9: 694, p. 6',1108,'[Nowicka]','','Species',NULL,'[761][762][763][764][765][766]','','SAG 85.79 = CCALA 026 = UTEX 2340',NULL,NULL,1,1,'clades:1109',1,'active','2022-01-20 12:43:14','admin'),(1111,'Arthrospira indica','Desikachary et Jeei Bai 1992. ETTA Nat. Symp., Madras: 15',108,'[311]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','2019-08-05 05:37:00','admin'),(1112,'Limnospira indica','(Desikachary et Jeeji Bai) Nowicka-Krawczyk, Mühlsteinová et Hauer 2019. Scientific Reports 9: 694, p. 7',1108,'','','Species',NULL,'[767]','','PCC 8005',NULL,NULL,0,1,'clades:1111',0,'active','2020-03-03 12:45:07','admin'),(1113,'Limnospira maxima','(Setchell et Gardner) Nowicka-Krawczyk, Mühlsteinová et Hauer 2019. Scientific Reports 9: 694, p. 7',1108,'','','Species',NULL,'[768][769][770]','','UTEX 2720 (sub. A. fusiformis)',NULL,NULL,0,1,'clades:1114',0,'active','2020-03-03 12:47:54','admin'),(1114,'Arthrospira maxima','Setchell et Gardner 1917. Univ. Calif. Publ. Bot. 6: 377',108,'[312]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1115,'Nunduva biania','León–Tejera, González–Resendiz et Johansen in González–Resendiz et al. 2018, Fottea 18(1): 89',1105,'[308]','Isotype: FCME–C708 (environmental sample).','Species',NULL,'','C708–M–10–K85 (UNAM)','FCME C708–M10–K85','Intertidal fringe; epilithic on granitic rock; Oaxaca: San Agustín Bay','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1116,'Nunduva britannica','Hauer in González-Resendiz et al. 2018, Fotte 18(1): 93',1105,'[308]','','Species',NULL,'','CBFS A–081–1','CCAP 1445/1','Brackish, estuarine; Newtown, Isle of Wright, England','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1117,'Phormidium corallyticum','Rützler et Santavy, 1983. &nbsp;Marine Ecology 4: 301',267,'[314]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1118,'Toxifilum','Zimba, Huang, Foley et Linton, 2017.<em>&nbsp;Journal of Phycology</em> 53(1): 190',1034,'[315]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:26:45','admin'),(1119,'Toxifilum mysidocida','Zimba, Huang, Foley et Linton, 2017. J. Phycol. 53(1): 190',1118,'[315]','','Species',NULL,'','PH NB2011F','','Benthic, &nbsp;from Rincon Bayou salt marsh, Nueces Bay, TX,','',1,1,'',0,'active','2020-12-07 07:57:15','admin'),(1120,'Potamolinea','Martins et Branco 2016, IJSEM 66(9): 3640',2555,'[155]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 10:34:19','admin'),(1121,'Heteroscytonema','McGregor et Sendal in Sendal &amp; McGregor 2018, Harmful Algae 80: 168',1122,'[318]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1122,'Heteroscytonemataceae','McGregor et Sendal in Sendal &amp; McGregor 2018, Harmful Algae 80: 168',9,'[318]','','Family',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1123,'Heteroscytonema crispum','&nbsp;(Bornet ex De Toni) McGregor &amp; Sendall in Sendall &amp; McGregor 2018, Harmful Algae 80: 169',1121,'[318]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1124',0,'active','2019-07-16 05:38:44','admin'),(1124,'Scytonema crispum','Bornet ex De Toni 1907 ex De Toni 1936',302,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1125,'Marileptolyngbya','Zhou et Ling 2018. Phytotaxa 383(1): 78',2544,'[319]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:34:31','admin'),(1126,'Marileptolyngbya sina','Zhou et Ling 2018. Phytotaxa 383(1): 78',1125,'[319]','','Species',NULL,'','CCTCC M 2015061 (cryopreserved material)','CCTCC M 2015061','epiphytic on Thalassia hemperichii','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1127,'Salileptolyngbya','Zhou 2018. Phytotaxa 383(1):79',2544,'[319]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:34:49','admin'),(1128,'Salileptolyngbya diazotrophica','Zhou 2018. Phytotaxa 383(1): 80',1127,'','','Species',NULL,'','CCTCC M 2017362 (cryopreserved)','CCTCC M 2017362','plankton-trawled 200-m deep seawater','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1129,'Capilliphycus','Caires, Sant´Anna et Nunes in <em>&nbsp;</em>Caires 2019, Notulae Algarum No. 95',2413,'[320][472]','','Genus',NULL,'[665]','','',NULL,NULL,0,1,'',0,'active','2022-01-14 13:15:32','admin'),(1130,'Capilliphycus salinus','&nbsp;Caires, Sant´Anna et Nunes in &nbsp;Caires 2019. Notulae Algarum No. 95',1129,'[320][472]','paratype: ALCB 103416','Species',NULL,'[666]','ALCB 114379','ALCB 114379','Epilithic in tidal pools with high salinity (50 psu) in the supralittoral zone; Bahia State, Pedra do Sal Beach, Salvador city','',1,1,'',0,'active','2019-11-28 07:48:37','admin'),(1131,'Capilliphycus tropicalis','Caires, Sant´Anna et Nunes in &nbsp;Caires 2019. Notulae Algarum No. 95',1129,'[472][320]','','Species',NULL,'[667]','ALCB 114392','ALCB 114392','Epilithic in protected reef region in mediolittoral zone; Bahia State, Camaçari city, Arembepe Beach','',0,1,'',0,'active','2019-11-28 07:48:56','admin'),(1132,'Schmidleinema cubanum','Folia Geobot. Phytotax., Praha, 24: 192',301,'[321]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1133,'Potamosiphon','G.B. McGregor &amp; B.C. Sendall 2019. Phytotaxa 387(2): 87',2553,'[322]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:28:09','admin'),(1134,'Potamosiphon australiensis','G.B. McGregor &amp; B.C. Sendall 2019. Phytotaxa 387(2): 87',1133,'[322]','','Species',NULL,'','BRI AQ826842','','small coastal stream in the Mary River catchment, rocks and other large debris from the stream bed','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1135,'Potamolinea magna','Martins et Branco 2016, IJSEM 66(9): 3640',1120,'[155]','','Species',NULL,'','SJRP 31642','','stream bottoms','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1136,'Lyngbya aerugieo-caerulea','Gomont, Ann. Sci. nat. 7, Bot. 16 : 146, 1892',234,'[235]','','Species',NULL,'','','','freshwater; rivers in <span lang=\'en\'><span title=\'\'>Campania</span></span>','[69]',0,1,NULL,0,'basionym','2020-01-06 09:00:44','admin'),(1137,'Potamolinea aerugineo-caerulea','(Gomont) Martins et Branco 2016. IJSEM 66(9): 3640',1120,'','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1136',0,'active','0000-00-00 00:00:00',NULL),(1138,'Capillus','T. A. Caires, C. L. Sant’Anna et J. M. C. Nunes 2018. Algae 33(4): 295',50,'[324]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1139,'Capillus salinus','T. A. Caires, C. L. Sant’Anna et J. M. C. Nunes 2018. Algae 33(4): 295',1138,'[324]','','Species',NULL,'','ALCB 114379','','Epilithic in tidal pools with high salinity (50 psu) in the supralittoral zone. This species formed large mats surrounding the full extent of the tidal pool.','',1,1,'',1,'deleted','0000-00-00 00:00:00',NULL),(1140,'Capillus tropicalis','T. A. Caires, C. L. Sant’Anna et J. M. C. Nunes 2018. Algae 33(4): 295',1138,'[324]','','Species',NULL,'','ALCB 114392','','Epilithic in protected reef region in mediolittoral zone.','',0,1,NULL,1,'deleted','0000-00-00 00:00:00',NULL),(1141,'Amazoninema','D. B. Genuário et al. 2020. IJSEM 70: 1441',2544,'[325][546]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 07:33:52','admin'),(1142,'Amazoninema brasiliense','D. B. Genuário et al. 2020. IJSEM 70: 1441',1141,'[325][546]','','Species',NULL,'','SP 428496','CMAA1602','freshwater from Amazon and Solimões rivers','',1,1,'',0,'active','2020-05-15 06:27:18','admin'),(1143,'Brasilonema geniculatum','Villanueva et Casamatta 2019. Phytotaxa 387(1): 9',118,'[326]','','Species',NULL,'','OL100180','UPOC 151/2014','Growing in a lichen-dominated consortium on granite cemetery tombstones','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1144,'Calothrix dumus','Villanueva et Casamatta 2019. Phytotaxa 387(1):12',119,'','','Species',NULL,'','OL 100181','UPOC 168/2015','Growing in lichen dominated consortia on granite cemetery tombstones','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1145,'Hassallia bouteillei','Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 5: 116',200,'','','Species',NULL,'','','','vertical chalk rocks','',0,1,NULL,0,'active','2019-10-04 05:13:10','admin'),(1146,'Limnothrix redekei','(van Goor) Meffert 1988. Arch. Hydrobiol./Algological Studies 50-53: 274',229,'','','Species',NULL,'','','SAG 3.89',NULL,NULL,1,1,'clades:1147',0,'active','0000-00-00 00:00:00',NULL),(1147,'Oscillatoria redekei','Van Goor 1918. Recl. Trav. bot. neerl. 15: 258',258,'[329]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1148,'Oscillatoria rosea','Utermöhl 1925. Arch. Hydrobiol., Suppl. 5: 285, nom. illeg.&nbsp;',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1149,'Oscillatoria planctonica','Woloszynska 1911. Bull. Acad. Sci. Cracoviae 1911: 530',258,'[327]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1150,'Limnothrix planctonica','(Woloszynska) Meffert 1988. Archiv f¨r Hydrobiologie/Algological Studies 50-53: 270',229,'[105]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1151,'Limnothrix rosea','(Utermöhl) Meffert 1988. Archiv für Hydrobiologie/Algological Studies 50-53: 274, nom. illeg.',229,'[105]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1148',0,'active','0000-00-00 00:00:00',NULL),(1152,'Chamaethrix','Dvořák et al. 2017. Fottea 17(2): 270',61,'[330]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1153,'Chamaethrix vaginata','Dvořák et al. 2017. Fottea 17(2): 270',1152,'[330]','','Species',NULL,'','OLM Botany 24: Lichenes and others No. 9225','UPOC F12/109','soil crust','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1154,'Foliisarcina','Alvarenga et al. 2016. IJSEM 66: 694',2557,'[332]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:28:39','admin'),(1155,'Foliisarcina bertiogensis','Alvarenga et al. 2016. IJSEM 66: 694',1154,'[332]','','Species',NULL,'','SP 429275','CENA 333','leaves of Avicennia schaueriana','',1,1,NULL,0,'active','2019-06-10 12:58:53','admin'),(1156,'Phylonema','Alvarenga et al. 2016. IJSEM 66: 695',36,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1157,'Phylonema aviceniicola','Alvarenga et al. 2016. IJSEM 66: 695',1156,'[332]','','Species',NULL,'','SP 429276','CENA 341','phylosphere of Avicennia','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1158,'Phylonema ansata','González-Resendiz, León-Tejera et Johansen 2018. Journal of Phycology 54: 641',1156,'[331]','','Species',NULL,'','FCME C58','','epilithic on supratidal and intertidal fringes','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1159,'Phylonema tangolundensis','González-Resendiz, León-Tejera et Johansen 2018. Journal of Phycology 54: 641',1156,'[331]','','Species',NULL,'','FCME C76','C76-M18-K59','epilithic on supratidal fringe','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1160,'Desmonostoc danxiaense','Cai et Li 2018. Phytotaxa 367(3): 237',710,'','nom. inval. (holotype designation missing)','Species',NULL,'','','CHAB 5868','Wet rocky wall in subtropical region.','',0,0,'',0,'active','0000-00-00 00:00:00',NULL),(1161,'Tolypothrix distorta','Kützing ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 5: 118',332,'[73]','','Species',NULL,'','','ACOI 731',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1162,'Geilterinema splendidum','(Greville ex Gomont) Anagnostidis 1989',186,'[464]','','Species',NULL,'[622]','epitype CBFS A–056-1','CCALA 1004',NULL,NULL,1,1,'',0,'active','2019-11-12 13:01:24','admin'),(1163,'Oscillatoria splendida','Greville ex Gomont 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 244',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1164,'Arthrospira jenneri','Stizenberger ex Gomont Ann. Sci. Nat. Bot., ser. 7, 16: 247',108,'[235][309]','','Species',NULL,'[773][774]','','','<span lang=\'en\'><span title=\'\'>ponds, lakes</span><span title=\'\'>,</span><span title=\'\'>&nbsp;reservoirs</span></span>','[92]',1,1,'',0,'active','2020-03-06 12:11:04','admin'),(1165,'Spirulina major','Kutzing ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 251',316,'','','Species',NULL,'[780][781][782][783]','','',NULL,NULL,1,1,'',0,'active','2020-03-16 13:32:34','admin'),(1166,'Aerosakkonema funiforme','Thu et Watanabe 2012. Phycologia 51(6): 675',1023,'[270]','','Species',NULL,'','EM block TNS-AL-57095','NIES2861','freshwater reservoir','[158]',1,1,'',0,'active','2021-06-18 10:44:52','admin'),(1167,'Planktothrix iranica','Heidari et Hauer 2018. Fottea 18(2): 139',272,'[335]','','Species',NULL,'','CBFS A–82–1','AS S8A','Benthic mat in the thermal spring (28 °C) with high natural radioactivity','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1168,'Nodosilinea radiophila','Heidari et Hauer 2018. Fottea 18(2): 142',565,'','','Species',NULL,'','CBFS A-83-1','TM S2B','Benthic mat in the thermal spring (27 °C) with very high natural radioactivity,','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1169,'Nodosilinea ramsarensis','Heidari et Hauer 2018. Fottea 18(2): 143',565,'[335]','','Species',NULL,'','CBFS A-84-1','KHS-S2.6','Soil around the thermal spring (32 °C)','',0,1,'',0,'active','2019-11-06 08:14:36','admin'),(1170,'Laspinema','Heidari et Hauer 2018. Fottea 18(2): 144',2257,'[335]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2020-10-13 06:34:31','admin'),(1171,'Laspinema thermale','Heidari et Hauer 2018. Fottea 18(2): 144',1170,'[335]','','Species',NULL,'','CBFS A-85-1','HK S5','Benthic mat in thermal springs','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1172,'Lapinema lumbricale','Heidari et Hauer 2018. Fottea 18(2): 145',1170,'[335]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1174',0,'active','0000-00-00 00:00:00',NULL),(1173,'Laspinema etoshii','(Dadheech, Casmatta, Casper et Krienitz) Heidari et Hauer 2018. Fottea 18(2): 145',1170,'[335]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:584',0,'active','0000-00-00 00:00:00',NULL),(1174,'Phormidium lumbricale','Casamatta, Johansen, Vis et Broadwater 2005. Journal of Phycology 41(2): 431',267,'[16]','','Species',NULL,'','BRY C-37699','UTCC 476',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1175,'Klisinema','Heidari et Hauer 2018. Fottea 18(2): 145',46,'[335]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:23:10','admin'),(1176,'Klisinema persicum','Heidari et Hauer 2018. Fottea 18(2): 145',1175,'[335]','','Species',NULL,'','CBFS A-86-1','SHAFA S10','Soil around thermal springs (50 °C) with high radiation background.','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1177,'Ramsaria','Heidari et Hauer 2018. Fottea 18(2): 146',2555,'[335]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:34:42','admin'),(1178,'Ramsaria avicennae','Heidari et Hauer 2018. Fottea 18(2): 146',1177,'[335]','','Species',NULL,'','CBFS A-087-1','','Benthic mat in thermal springs (35 °C) with high radiation background','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1179,'Persinema','Heidari et Hauer 2018. Fottea 18(2): 146',2546,'[335]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','2023-01-31 08:13:10','admin'),(1180,'Persinema komarekii','Heidari et Hauer 2018. Fottea 18(2): 146',1179,'[335]','','Species',NULL,'','CBFS A-88-1','TM S1','Benthic mat in thermal springs (27 °C) with high radiation background.','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1181,'Macrochaete','Berrendero, Johansen et Kastovsky in Berrendero et al. 2016, J. Phycol. 52(4): 641',36,'[337]','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1182,'Macrochaete lichenoides','Berrendero, J.R.Johansen &amp; Kastovsky in Berrendero et al. 2016, J. Phycol. 52(4): 644',1181,'[337]','','Species',NULL,'','CBFS A-049','SAG 32.92','lichen phycobiont, Punta del Papagayo, Lanzarote,','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1183,'Leptolyngbya angustata','Casamatta et Johansen 2005. Journal of Phycology 41: 430',225,'[16]','','Species',NULL,'','BRY C-37697','UTCC 473',NULL,NULL,0,1,NULL,1,'active','2019-05-29 12:56:50',NULL),(1184,'Macrochaete psychrophila','Berredero, .Johansen et Kastovsky in Berrendero et al. 2016, J. Phycol. 52(4): 642',1181,'[337]','','Species',NULL,'','CBFS A-048','CCALA 1092','epilithic, soil surface and biological soil crust in cold environments - high mountains','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1185,'Macrochaete santannae','Berrendero, Johansen et Kastovsky in Berrendero et al. 2016, J. Phycol. 52(4): 642',1181,'[337]','','Species',NULL,'','CBFS A-050','CCALA 1093.','Epilithic, on an exposed vertical igneous rock surface receiving periodic moisture; Rodovia dos Tamoios, Caraguatatuba, Sao Paulo State','[172]',0,1,NULL,0,'active','2021-06-18 09:21:35','admin'),(1186,'Parthasarathiella db-testing','Říha 2019',263,'[299]','This is not a species: this is just the app being tested...','Species','[27]','[185][178]','HRB01','XY001',NULL,NULL,0,0,'',1,'deleted','0000-00-00 00:00:00',NULL),(1187,'Oxynema aestuarii','Chakraborty et Mukherjee 2018. Phytotaxa 374(1): 37',471,'[338]','','Species',NULL,'','cryopreserved MCC 3874','','soil surface biofilm in brackish water (salinity 1.5%).','',0,1,NULL,0,'active','2020-03-02 13:31:17','admin'),(1188,'Stigonema mamillosum','Agardh ex Bornet et Flahault 1886. Revision des Nostocacées &nbsp;hétérocystées contenues dans les principaux herbiers de France &nbsp;(Troisième fragment). <em>Annales des Sciences Naturelles, Botanique, Septième série</em> 5:&nbsp; 77',321,'','','Species',NULL,'','','',NULL,NULL,1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1189,'Petalonema alatum','Berkeley ex Correns, 1889. Flora 72: 321.',265,'[339]','','Species',NULL,'','','','shady places on wet limestone rocks','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1190,'Fortiea contorta','Hauer, Bohunická et Mareš 2014. Journal of Phycology 50:1094',182,'[73]','','Species',NULL,'','CBFS A-024-1','PCC 7126',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1191,'Fortiea laiensis','Vaccarino et Johansen 2014. Journal of Phycology 50: 1096',182,'[73]','','Species',NULL,'','BISH 750698','','waterfall','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1192,'Fortiea coimbrae','Hauer, Bohunická et Mareš 2014. Journal of Phycology 50:1097',182,'','','Species',NULL,'','CBFS A-018-1','ACOI 1451','vase with Chara sp.','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1193,'Iningainema pulvinus','McGregor et Sendall, 2017. Harmful Algae 62: 17',613,'[169]','','Species',NULL,'','AQ522230','ES0614','freshwater ambient spring wetland, Edgbaston Reserve','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1194,'Oscillatoria lloydiana','Gomont, 1899, Bull. Soc. Bot. France 46: 39',258,'[224]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1195,'Oscillatoria acuminata','Gomont 1892, Ann. Sci. Nat. Bot., ser. 7, 16: 227',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1196,'Oscillatoria animalis','Agard ex Gomont 1892, <em>Ann. Sci. Natur., Botanique, Série 7,</em> 16: 227-228',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1197,'Oscillatoria chlorina','Kützing 1843, &nbsp;Phycologia generalis, p. 185',258,'[135]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1198,'Oscillatoria cortiana','Meneghini, 1837, Coment. Med. Dot. Spongia 4: 326',258,'[340]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1199,'Oscillatoria formosa','Bory, 1827, Dict. Class. d´Hist. Nat. 12: 474',258,'[341]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1200,'Oscillatoria jasorvensis','Vouk, 1919, &nbsp;Jugosl. Akad. Prirod. Istr.Hrvatske i Slovenie, Mat. Prir.Razr. 14: 128',258,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1201,'Oscillatoria laetevirens','Crouan et Crouan, 1867, Fl. Finistére p. 112',258,'[342]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1202,'Oscillatoria okenii','Agardh, 1827, Flora oder Botanische Zeitung 10(40): 633-634',258,'[343]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1203,'Phormidium pavlovskoense','Elenkin, 1949, Monogr. Alg. Cyanoph. Aquidulc. Terr. URSS, Fasc. 2, 1501–1502',267,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1204,'Oscillatoria proteus','Skuja, 1949, N. Acta Reg. Soc. Sci. Upsal., ser. 4, 14(5): 48',258,'[344]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','2019-11-15 13:18:54','admin'),(1205,'Anabaena bergii','Ostenfeld 1908, Scientific Results of the Aral Sea Expedition 8: 142',102,'[345]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1206,'Aphanizomenon ovalisporum','Forti 1911, <em>Atti Mem. Accad. Agric. Sci. Lett., Arti Comm. Verona, Series IV</em> 12: &nbsp;3-5',104,'[346]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1207,'Anabaena bergii var. minor','Kiselev 1927, Bull. Sect. Ichthyol. appl. Etud. scient. -ind. (U)<em>2</em>, 279',102,'[347]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1208,'Lyngbya murrayi','W. et G.S.West, &nbsp;1911, Brit. Antarct. Exp. 1: 289',234,'','','Species',NULL,'','','','free-floating, Green Lake','',0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1209,'Ewamiania','McGregor &amp; Sendall 2017. Australian Systematic Botany 30(1):43',37,'','','Genus',NULL,'','','',NULL,NULL,0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1210,'Ewamiania thermalis','McGregor &amp; Sendall 2017. Australian Systematic Botany 30(1):46',1209,'[348]','','Species',NULL,'','BRI AQ522229','','thermal spring','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1211,'Pleurocapsa fuliginosa','Hauck, 1885. Rabenhorst´s Kryptogamenfl., ed. 2, 2: 515.',274,'[350][349]','','Species',NULL,'','neotype BISH 755070','HA4302-MV1','Rock face near the stream/wet [Shalygin et al. 2019]','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1212,'Limnococcus limneticus','(Lemmermann) Komárková, Jezberová, Komárek et Zapomělová 2010, Hydrobiologia 639:&nbsp;',228,'[38]','','Species',NULL,'','','CCALA No. 890',NULL,NULL,1,1,'clades:1213',0,'active','0000-00-00 00:00:00',NULL),(1213,'Chroococcus limneticus','Lemmermann, Bot. Zentralbl. 76: 153, 1898',130,'[252]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1214,'Limnococcus cumulatus','(Bachmann) Plinski et Komárek 2017, Cyanobacteria of the Gulf of Gdansk and southern Baltic, p. 145',228,'[351]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1215',0,'active','0000-00-00 00:00:00',NULL),(1215,'Chroococcus cumulatus','Bachmann, 1921, Mitt. Naturf. Ges. Luzern 8: 11',130,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'basionym','0000-00-00 00:00:00',NULL),(1216,'Pleurocapsa minor','Hansgirg 1891. Věst. Král. české pol. nauk, třída mathematicko-přírodovědecká 1890(2): 89',274,'[352][349]','','Species',NULL,'','epitype BISH 751766','HA4230-MV1','on stones in springs near Prague (Malá Chuchle, Radotín) [Hanshirg 1891]','',0,1,'',0,'active','2019-07-19 05:47:29','admin'),(1217,'Limnococcus distans','(Smith) Plinski et Komárek 2017, Cyanobacteria of the Gulf of Gdansk and southern Balt, p. 145',228,'[351]','','Species',NULL,'[271]','','',NULL,NULL,0,1,'clades:1218',0,'active','0000-00-00 00:00:00',NULL),(1218,'Chroococcus limneticus var. distans','Smith 1916, Bull. Torrey Bot, Club 43:481',130,'[353]','','Species',NULL,'','','','plankton, Birch, Soft and Tamarack lakes','',0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1219,'Kyrtuthrix dalmatica','Ercegović 1929. Arch. Protistenk. 66 (1): 170',222,'[354]','','Species',NULL,'','','','limestone in a splash zone [Ercegović 1929]','',1,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1220,'Limnococcus dispersus','(Keissler) Plinski et Komárek 2017, Cyanobacteria of the Gulf of Gdansk and southern Balt, p. 144',228,'[351]','','Species',NULL,'[272]','','',NULL,NULL,0,1,'clades:1221',0,'active','2019-06-10 05:41:22','admin'),(1221,'Chroococcus minor var. dispersus','Keissler 1902, Verh. Zool. - Bot. <a href=\'//Zool.-Bot\'></a> Ges, Vien 52: 311',130,'[355]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1222,'Brachytrichia maculans','Gomont 1902. Bot. Tidskrift 24: 210',116,'[356]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'basionym','0000-00-00 00:00:00',NULL),(1223,'Kyrtuthrix maculans','(Gomont) Umezaki 1958: 64',222,'','','Species',NULL,'','PC 0123984','','marine littoral','',0,1,'clades:1222',0,'active','0000-00-00 00:00:00',NULL),(1224,'Kyrtuthrix huatulcensis','León-Tejera, González-Resendiz et Johansen 2016. Phytotaxa 278(1): 8',222,'[358]','','Species',NULL,'','FCME-PTM C708','','Supratidal and intertidal fringes; epilithic on granitic rock. [León-Tejera et al. 2016]','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1225,'Leptolyngbya indica','Debnath et Bhadury 2017. Phytotaxa 316(2): 105',225,'[359]','','Species',NULL,'','IISER Kolkata VSP 006','IISER Kolkata IISER Kolkata','early soil crust in arsenic affected alluvial rice field','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1226,'Dolichospermum hangangense','H.J. Choi &amp; M.-S. Han 2020. Notulae Algarum 124',172,'[360][542]','','Species',NULL,'','fixed material of strain HYCP1307-DH5','HYCP1307-DH5','plankton','',0,1,'',0,'active','2020-05-14 12:31:13','admin'),(1227,'Romeria leopoliensis','(Raciborski) Koczwara in Geitler 1932:916',297,'','','Species',NULL,'[777][778][779]','','','planktic; in einem See bei Lwów','[118]',1,1,NULL,0,'active','2020-03-16 12:21:37','admin'),(1228,'Romeria minima','(Lemmermann) Komárek 2001. Czech Phycology 1: 7',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1229,'Romeria alascensis','(Hortobágy et Hilliard) Komárek 2001. Czech Phycology 1: 7',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1230,'Romeria caruaru','Komárek, S.M.F.O. Azevedo, P. Domingos, Komárková, et M. Tichý 2001. Algologica Studies 103: 14&nbsp;',297,'[27][362]','','Species',NULL,'','BRNM HY-1201','','plankton','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1231,'Romeria chlorina','Böcher 1949. Kong. danske Vidensk. Selsk., biol., 21(1): 26',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1232,'Romeria cylindrocellularis','Hindák 1988. Preslia 60: 295',297,'[27]','','Species',NULL,'','iconotype Fig. 3: 1','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1233,'Romeria westii','(Kufferath) Anagnostidis 2001. Preslia 73: 360',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1234,'Romeria gracilis','(Koczwara) Koczwara ex Geilter 1932. Rabenh.’s Krypt.-Fl. 14: 916.',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1235,'Romeria hieroglyphica','Komárek et Komárková-Legnerová 2007. Hoehnea 34(1): 50',297,'','','Species',NULL,'','SP 355744','','plankton in small shallow pond on pastures','',0,1,'',0,'active','0000-00-00 00:00:00',NULL),(1236,'Romeria cryophila','Kol 1966. Ann. hist.-nat. Mus. Nat. Hung., Bot. (Budapest) 58: 161-168',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1237,'Romeria simplex','(Hindák) Hindák 1988. Presla 60: 299',297,'[27]','','Species',NULL,'','iconotype Hindák 1975 tab. 7, fig. 1','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1238,'Romeria victoriae','Komárek et Cronberg 2001. Nova Hedwigia 73: 141',297,'[27]','','Species',NULL,'','iconotype Komárek & Cronberg 2001, fig. 13b','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1239,'Romeria elegans','(Woloszynska in Koczwara) Woloszynska et Koczwara ex Geilter 1932. Rabenh.’s Krypt.-Fl. 14: 916',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1240,'Romeria nivicola','(Kol) O. Komárek et Komárek 2001. Nova Hedwigia Beiheft 123 :131',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1241,'Romeria heterocellularis','Komárek 2001',297,'[27]','no formal description','Species',NULL,'','','',NULL,NULL,0,0,NULL,0,'active','0000-00-00 00:00:00',NULL),(1242,'Romeria austriaca','Claus 1961. Int. Rev. ges. Hydrobiol. 46(4): 520',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1243,'Romeria crassa','Hindák 1988. Preslia 60: 299',297,'[27]','','Species',NULL,'','iconotype Hindák 1988, fig. 5','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1244,'Romeria okensis','(Meyer) Hindák 1975. Arch Hydrobiol./Algological Studies 13: 340',297,'[27]','','Species',NULL,'[823]','','',NULL,NULL,0,1,'clades:2063',0,'active','2020-03-20 10:01:47','admin'),(1245,'Romeria mexicana','(Rouchijainen) Komárek 2001. Czech Phycology 1: 10',297,'[27]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1246,'Romeria obruseacuminata','(Starmach) Komárek in Anagnostidis 2001. Preslia 73: 374',297,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1247,'Komvophoron hindakii','Hašler et Poulíčková 2010',221,'[103][363]','does not meet requirements of art. 7.11 of ICN; ambiguous type designation','Species',NULL,'','','','Epipelic species in stagnant freshwaters, usually on mud with higher portion of organic compounds under aerobic conditions.','',0,0,'',0,'active','0000-00-00 00:00:00',NULL),(1248,'Pycnacronema','M.D. MArtins et Branco 2019. Journal of Phycology 55: 152',2555,'[364]','','Genus',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:34:31','admin'),(1249,'Pycnacronema brasiliensis','M.D. Martins et Branco 2019. Journal of Phycology 55: 152',1248,'[364]','','Species',NULL,'','SJRP 31641','45PC','on barks of trees and wet rocks','',1,1,'',0,'active','0000-00-00 00:00:00',NULL),(1250,'Pycnacronema arboriculum','M.D. Martins et Branco 2019. Journal of Phycology 55: 153',1248,'[364]','','Species',NULL,'','SJRP 31885','41PC','on barks of trees','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1251,'Pycnacronema conicum','M.D. MArtins et Branco 2019. Journal of Phycology 55: 155',1248,'[364]','','Species',NULL,'','SJRP 31652','7PC','on barks of trees','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1252,'Pycnacronema marmoreum','M.D. Martins et Branco 2019. Journal of Phycology 55: 155',1248,'[364]','','Species',NULL,'','SJRP 31651','42PC','on barks of trees','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1253,'Pycnacronema rubrum','M.D. Martins et Branco 2019. Journal of Phycology 55: 155',1248,'[364]','','Species',NULL,'','SJRP 31640','43PC','bark of trees','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1254,'Pycnacronema savanensis','M.D. Martins &amp; Branco 2019. Journal of Phycology 55: 155',1248,'[364]','','Species',NULL,'','SJRP 31884','49PC','soil crust','',0,1,NULL,0,'active','0000-00-00 00:00:00',NULL),(1278,'$ DEBUGGING...','Hobit 2019',1,'[301]','The CyanoDB is being debugged','Species',NULL,'[3]','xxx','yyy',NULL,NULL,1,0,'clades:502',1,'active','2019-04-18 17:45:01','admin'),(1279,'Phormidium molle','Gomont 1892. Ann. Sci. Nat. Bot., ser. 7 (16): 163.',258,NULL,NULL,'Species',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2019-05-24 19:26:31',NULL),(1280,'Phormidium molle','Gomont 1892. Ann. Sci. Nat. Bot. Ser. 7, 16: 163',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-04-24 14:56:42',NULL),(1281,'Phormidesmis mollis','(Gomont) Turicchia, Ventura, Komárková et Komárek 2009. Nova Hedwigia 89: 179',667,'[178]','','Species',NULL,'','','3CC04S05',NULL,NULL,1,1,'clades:1280',0,'active','2019-07-15 07:14:13','admin'),(1282,'Phormidesmis communis','Raabová, Kováčik, Elster et Strunecký 2019. Phytotaxa 395(1): 12',667,'[365]','the description does not meet requiremets of art. 8.4 of the ICN','Species',NULL,'','','AB 11-10',NULL,NULL,0,0,'',0,'active','2019-04-24 15:18:38',NULL),(1283,'Phormidesmis antarctica','Raabová, Kováčik, Elster et Strunecký 2019. Phytotaxa 395(1): 12',667,'[365]','the description does not meet requiremets of art. 8.4 of the ICN','Species',NULL,'','','CCALA 1101',NULL,NULL,0,0,'',0,'active','2019-04-24 15:22:44',NULL),(1284,'Phormidesmis nigrescens','Raabová, Kováčik, Elster et Strunecký 2019. Phytotaxa 395(1): 12',667,'[365]','the description does not meet requiremets of art. 8.4 of the ICN','Species',NULL,'[537]','','CCALA 1102',NULL,NULL,0,0,'clades:1329',0,'active','2019-07-17 11:09:38','admin'),(1285,'Leptodesmis','Raabová, Kováčik, Elster et Strunecký 2019. Phytotaxa 395(1): 13',61,'[365]','the description does not meet requiremets of art. 8.4 of the ICN','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2019-05-06 04:57:25','admin'),(1286,'Leptodesmis paradoxa','Raabová, Kováčik, Elster et Strunecký 2019. Phytotaxa 395(1): 13',1285,'[365]','the description does not meet requiremets of art. 8.4 of the ICN','Species',NULL,'','','',NULL,NULL,1,0,'',0,'active','2019-05-06 04:57:29','admin'),(1287,'Dapis','Engene, Tronholm et V.J. Paul 2018. Journal of Phycology 54: 443',50,'[366]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-05-06 04:55:54','admin'),(1288,'Dapis pleousa','Engene, Tronholm et V.J. Paul 2018. Journal of Phycology 54: 443',1287,'[366]','','Species',NULL,'','US 223311','FFP12-7','common in tropical and subtropical marine habitats, in shallow (&gt;2 m) and calm waters. Typically grows on intertidal, soft bottom habitats, and can also grow epiphytically on seagrass or macroalgae or float on ocean surface. Seasonally it can form exte','[113]',1,1,'',0,'active','2019-05-06 04:55:27','admin'),(1289,'Dapis pnigousa','Engene, Tronholm et V.J. Paul 2018. Journal of Phycology 54: 444',1287,'[366]','','Species',NULL,'','US217967','BCBC12-12','common coral reefs environments, in deeper waters (12–30 m depth)','[113]',0,1,'',0,'active','2019-05-06 04:55:32','admin'),(1290,'Oculatella ucrainica','O.M. Vynogradova et Mikhailyuk 2017. Ukrainian Botanical Journal 74(6): 518',478,'[367]','','Species',NULL,'','KW-A 32375','SAG 2563','biological crusts dominated by Nostoc edaphicum and Hassalia sp. on the surface of coquina, clay and chalk outcrops, and hypolitically under pieces of quartz','[118]',0,1,'',0,'active','2019-05-10 05:23:03','admin'),(1291,'Oculatella kazantipica','O.M. Vynogradova et Mikhailyuk 2017. Ukrainian Botanical Journal 74(6): 518',478,'[367]','','Species',NULL,'','KW-A 32376','SAG 2567','coquina beach exposed to direct sunlight, in biological crusts with dominance of <em>Microcoleus vaginatus</em> at seaside.','[118]',0,1,'',0,'active','2019-05-10 05:22:47','admin'),(1292,'Plectonema tomasinianum','Bornet ex Gomont',273,'[235]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-05-10 05:23:34','admin'),(1293,'Plectonema boryanum','Gomont 1899. <em>Bulletin de la Société Botanique de France</em> 46: &nbsp;36',273,'[224]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-10 05:23:28','admin'),(1294,'Leptolyngbya boryana','(Gomont) Anagnostidis et Komárek 1988. Arch. Hydrobiol./Algological Studies 50-53): 391',225,'[102]','','Species',NULL,'','','NIES-2135',NULL,NULL,1,1,'clades:1293',0,'active','2019-05-10 05:21:33','admin'),(1295,'Aphanothece atro-crustacea','Skuja 1964, Nova Acta Reg. Soc. Sci. Upsal. ser. 4 18(3)',106,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-23 12:12:28',NULL),(1296,'Aphanothece bacilloidea','Gardner 1927, Mem. New York Bot. Gard. 7: 5',106,'[215]','','Species',NULL,'','','','depressions in limestone','',0,1,NULL,0,'active','2019-05-23 12:23:01',NULL),(1297,'Aphanocapsa parietina','Nägeli 1849. Gattungen der einzelliger Algen: 52',105,'[115]','','Species',NULL,'','protologue Tab. I B, fig. 1','',NULL,NULL,1,1,'',0,'active','2019-06-05 13:01:52','admin'),(1298,'Cyanosarcina fontana','L. Kováčik 1988. Arch. Hydrobiol./Algological Studies 50-53: 176',159,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-05 13:02:33','admin'),(1299,'Symploca muralis','Kützing ex Gomont 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 112',324,'[235]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-06-05 12:59:06','admin'),(1300,'Pleurocapsa muralis','Lagerheim in Wittrock et Nordstedt. 1893. Alg. Exs. <strong>23</strong>: 1097',274,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-06-06 12:57:04','admin'),(1301,'Nostoc commune','Vaucher ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot. ser. 7, 7: 203',255,'','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-06-05 12:57:34','admin'),(1302,'Leptolyngbya aeruginea','(Kützing ex Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'[467]','','',NULL,NULL,0,1,'clades:1304',0,'active','2019-05-24 12:05:19',NULL),(1303,'Paracapsa siderophila','Naumann 1924. Arkiv för Botanik 18(21): 6',261,'[368]','','Species',NULL,'','','','benthic in a lake, on stones with iron','[90]',1,1,'',0,'active','2019-06-06 12:43:47','admin'),(1304,'Lyngbya aeruginea','Kützing ex Hansgirg 1892, 88',234,'[275]','','Species',NULL,'[466]','','','swamp, warm and cold water','',0,1,'',0,'active','2019-05-24 11:58:50',NULL),(1305,'Leptolyngbya africana','&nbsp;(Lemmermann) Anagnostidis &amp; Komárek 1988',225,'[102]','','Species',NULL,'[471]','','',NULL,NULL,0,1,'clades:1306',0,'active','2019-05-27 11:24:45',NULL),(1306,'Phormidium africanum','Lemmermann 1914, Wiss. Ergebn. Dt. Zentr. Afr. Exp. 1907-1908, 2: 89',267,'[369]','','Species',NULL,'','','','Lake Kivu, hot springs','',0,1,'',0,'active','2019-05-24 13:09:24',NULL),(1307,'Leptolyngbya amplivaginata','(Van Goor) Anagnostidis et Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'[469][468][470]','','',NULL,NULL,0,1,'clades:1308',0,'active','2019-05-27 08:46:15',NULL),(1308,'Lyngbya amplivaginata','Van Goor 1918, Réc. Trav. Bot. Néerl. 15: 257',234,'[329]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-27 08:21:49',NULL),(1309,'Leptolyngbya angusta','Anagnostidis 2001, Preslia 73(4): 364',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1310',0,'active','2019-05-27 08:45:25',NULL),(1310,'Lyngbya perelegans var. angusta','Skuja 1964, Nova Acta Reg. Soc. Sci. Upsal., ser. 4, l8 (3): 58',234,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-07-23 04:13:20','admin'),(1311,'Leptolyngbya angustata','Casamatta et Johansen in Casamatta et al. 2005, J. Phycol 41(2): 430-431',225,'[16]','','Species',NULL,'','BRY C-37697','UTCC473','Benthic substrate of Kuparuk River, near Toolik Lake','',0,1,NULL,0,'active','2019-05-27 10:50:34',NULL),(1312,'Leptolyngbya angustissima','(West &amp; G.S.West) Anagnostidis et Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'[472][474][473]','','',NULL,NULL,0,1,'clades:1313',0,'active','2019-05-27 12:23:03',NULL),(1313,'Phormidium angustissimum','West et West, 1897. J. Bot. 35: 298',267,'[370]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-27 11:45:54',NULL),(1314,'Leptolyngbya antarctica','(West &amp; G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1315',0,'active','2019-05-27 12:35:43',NULL),(1315,'Phormidium antarcticum','West &amp; G.S.West 1911, British. Antarct. Exped. 1(7): 292',267,'[282]','','Species',NULL,'','','','Pony Lake','',0,1,NULL,0,'active','2019-05-27 12:34:25',NULL),(1316,'Leptolyngbya appalachiana','Johansen &amp; Olsen in Johansen et al. 2008, Algolog. Stud. 126: 24, 26',225,'[22]','','Species',NULL,'','BRY C37679','GSM-SFF-MF60','quartzite seep wall on Cataloochie Road, Great Smoky Mts. National Park, Haywood County, North Carolina','',0,1,NULL,0,'active','2019-05-27 13:03:50',NULL),(1317,'Leptolyngbya aspera','(Schwabe) Anagnostidis 2001, Preslia 73: 364',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1318',0,'active','2019-05-27 13:19:08',NULL),(1318,'Lyngbya ferruginea var. aspera','Schwabe 1944, <em>Mitteilungen der deutschen Gesellschaft für Natur- und Völkerkunde Ostasiens</em>, Suppl. 21: 178',234,'[371]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-27 13:18:40',NULL),(1319,'Leptolyngbya batrachosperma','Anagnostidis 2001, Preslia 73: 364',225,'[9]','Holotypus (protologus): Skuja 1926, Acta Horti. Bot. Univ. Latv. 1: 176','Species',NULL,'[475]','','','','',0,1,'',0,'active','2019-05-28 13:25:11',NULL),(1320,'Leptolyngbya benthonica','(Skuja) Anagnostidis 2001, Preslia 73: 364',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1321',0,'active','2019-05-29 08:07:31',NULL),(1321,'Lyngbya bipunctata var. benthonica','Skuja 1964, Nova Acta Reg. Soc. Sci. Univ. Upsal., ser. 4, 18(3): 57',234,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-05-29 08:06:59',NULL),(1322,'Leptolyngbya bigranulata','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'[476][477]','','',NULL,NULL,0,1,'clades:1323',0,'active','2019-05-29 11:00:09',NULL),(1323,'Phormidium bigranulatum','Gardner 1926, Rhodora 28: 2',267,'[372]','','Species',NULL,'','','','Growing on or within the gelatinous tegument of <em>Rivularia (Gloeotrichia) indica</em>, attached to submerged aquatic plants','',0,1,'',0,'active','2019-05-29 10:45:14',NULL),(1324,'Leptolyngbya bijahensis','(Copeland) Anagnostidis 2001, Preslia 73(4): 364',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1325',0,'active','2019-05-29 11:27:58',NULL),(1325,'Phormidium bijahense','Copeland 1936, Ann. N.Y. Acad. Sci. 36: 188',267,'[374]','','Species',NULL,'','','','thermal springs','',0,1,'',0,'active','2019-05-29 11:27:32',NULL),(1326,'Leptolyngbya blennophila','Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','nomen novum','Species',NULL,'[478]','','',NULL,NULL,0,1,'',0,'active','2019-05-30 08:22:04',NULL),(1327,'Leptolyngbya borchgrevinkii','Komárek 2007, Polish Polar Rerearch 28(3): 226',225,'[375]','holotypus hic designatus: figura nostra 8a–h (iconotypus)','Species',NULL,'','BRNM/HY 1414','','slowly streaming and shallow water, wetlands of maritime Antarctic','',0,1,'',0,'active','2019-05-29 12:20:42',NULL),(1328,'Leptolyngbya vincentii','Komárek 2007, Polish Polar Research 28(3): : 219',225,'[375]','holotypus hic designatus: figura nostra 4a–h (iconotypus)','Species',NULL,'','BRNM−HY 1411','','seepages in maritime Antarctic','',0,1,NULL,0,'active','2019-05-29 12:25:29',NULL),(1329,'Leptolyngbya nigrescens','Komárek 2007, Polish Polar Research 28(3): 221',225,'[375]','holotypus hic designatus: figura nostra 6a–b (iconotypus)','Species',NULL,'','BRNM−HY 1412','','Subaerophytic, on wet rock, less frequently on soil and the surface of mats in seepages','',0,1,'',0,'active','2019-05-29 12:39:17',NULL),(1330,'Leptolyngbya fritschiana','&nbsp;Komárek 2007, Polish Polar Research 28(3): 224',225,'[375]','holotypus hic designatus: figura nostra 7a–h (iconotypus)','Species',NULL,'','BRNM−HY 1413','','in streaming waters, at the edge of streams, up to subaerophytic','',0,1,'',0,'active','2019-06-05 13:24:32','admin'),(1331,'Leptolyngbya andina','(Schwabe) Anagnostidis 2001, Preslia 73(4): 364',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1332',0,'active','2019-05-30 07:06:32',NULL),(1332,'Plectonema andinum','Schwabe 1960, Nova Hedwigia 2: 257',273,'[376]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-30 07:13:02',NULL),(1333,'Leptolyngbya badia','Johansen &amp; Lowe in Johansen et al. 2008, Algolog. Stud. 126: 26',225,'[173]','','Species',NULL,'','BRY C 37684','','quartzite stepp wall on Cataloochie Road, Great Smoky Mts. Nat. Park, Haywood Country, North Carolina','',0,1,'',0,'active','2019-05-30 07:52:18',NULL),(1334,'Leptolyngbya bijugata','(Kongisser) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:569',0,'active','2019-05-30 08:21:20',NULL),(1335,'Leptolyngbya borodinii','(Kongisser) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1336',1,'active','2019-05-30 10:49:46',NULL),(1336,'Lyngbya borodinii','Kongisser 1931, J. Soc. bot. Russie 16(5-6): 502',234,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-05-30 08:43:39',NULL),(1337,'Limnothrix borodinii','(Kongisser) Anagnostidis 2001, Preslia 73: 360',229,'[9]','','Species',NULL,'[479]','','',NULL,NULL,0,1,'clades:1336',0,'active','2019-05-30 10:45:38',NULL),(1338,'Leptolyngbya breviarticulata','&nbsp;(Claus) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1339',0,'active','2019-05-30 11:06:39',NULL),(1339,'Phormidium treleasei f. breviarticulatum','Claus 1961, Int. Rev. Ges. Hydrobiol. 46(4): 526',267,'[377]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-30 11:06:12',NULL),(1340,'Leptolyngbya calotrichoides','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1341',0,'active','2019-05-30 11:22:05',NULL),(1341,'Plectonema calotrichoides','Gomont 1899, Bull. Soc. Bot. France 46: 30',273,'[224]','','Species',NULL,'','','','maritimas America','',0,1,NULL,0,'active','2019-05-30 11:20:56',NULL),(1342,'Plectonema carneum Kützing ex Lemmermann 1910: 206','Kützing ex Lemmermann 1910, Krypt.-Fl. Mark Brandenb. 3: 206',273,'[378]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-05-30 11:36:36',NULL),(1343,'Leptolyngbya carnea','(Kützing ex Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud.: 391',225,'[102]','','Species',NULL,'[481][480][482]','','',NULL,NULL,0,1,'clades:1342',0,'active','2019-05-30 11:43:34',NULL),(1344,'Leptolyngbya cartilaginea','&nbsp;(Copeland) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1345',0,'active','2019-05-30 12:26:03',NULL),(1345,'Phormidium valderianum var. cartilagineum','&nbsp;Copeland 1936, Ann. NY Acad. Sci. 36: 180',267,'[374]','','Species',NULL,'','','','thermophilic, slope of Bijou geyser, Yellowstone Nat. Park','',0,1,NULL,0,'active','2019-05-30 12:24:35',NULL),(1346,'Leptolyngbya cataractarum','(Rabenhorst ex Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'[483][484]','','',NULL,NULL,0,1,'clades:1347',0,'active','2019-05-30 12:56:16',NULL),(1347,'Lyngbya cataractarum','Rabenhorst ex Hansgirg, 1892, <em>Arch. naturwis. Landesdurchforschung von Böhmen</em> 8(4): 91',234,'[275]','','Species',NULL,'','','','wet rocks, Teplice','',0,1,NULL,0,'active','2019-05-30 12:42:30',NULL),(1348,'Leptolyngbya cebennensis','(Gomont) Umezaki &amp; Watanabe 1994, Jpn. J. Phycol. 42: 203',225,'[231]','','Species',NULL,'[485]','','',NULL,NULL,0,1,'clades:1349',0,'active','2019-05-30 13:25:36',NULL),(1349,'Phormidium cebennense','Gomont 1899, Bull. Soc. Bot. France 46: 38',267,'[224]','','Species',NULL,'','','','wet granit rocks','',0,1,NULL,0,'active','2019-05-30 13:21:33',NULL),(1350,'Leptolyngbya chlorina','(Perfiliev) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1351',0,'active','2019-05-31 10:29:24',NULL),(1351,'Lyngbya chlorina','Perfiliev 1923, Bull. Kom. Sapropel. Leningr. 1: 63',234,'','','Species',NULL,'','','',NULL,NULL,0,1,NULL,0,'active','2019-05-31 10:29:01',NULL),(1352,'Leptolyngbya circularis','McGregor 2007, Flora Australia, Suppl. 24: 29',225,'[45]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-03 08:02:12',NULL),(1353,'Leptolyngbya compacta','(Hansgirg ex Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'[487][488][489]','','',NULL,NULL,0,1,'',0,'active','2019-06-03 09:04:03',NULL),(1354,'Lyngbya compacta','Hansgirg ex Hansgirg 1892, Prodromus, p. 88',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-03 08:24:26',NULL),(1355,'Leptolyngbya copelandii','Anagnostidis 2001, Preslia 73(4): 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1356',0,'active','2019-06-04 06:08:24','admin'),(1356,'Phormidium truncatum var. thermale','.Copeland 1936, Ann. N.Y. Acad. Sci.36: 181-182',267,'[374]','type no. 440','Species',NULL,'','','','thermophilic (48.3\' C, pH. 9.0) Bijou Geyser cone, Upper Geyser Basin, Yellowstone Nat. Park','',0,1,'',0,'active','2019-06-04 06:10:47','admin'),(1357,'Leptolyngbya corticola','&nbsp;Johansen et Kováčik in Johansen et al. 2011, Nova Hedwigia 92(2-4): 291',1,'[118]','','Species',NULL,'','BRY 37704','CCALA 085',NULL,NULL,0,1,'',1,'active','2019-06-03 12:25:55','admin'),(1358,'Leptolyngbya crassior','&nbsp;(Skuja) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1359',0,'active','2019-06-04 06:08:38','admin'),(1359,'Lyngbya perelegans var. crassior','&nbsp;Skuja 1964, Nova Acta Reg. Soc. Sci. Upsal. ser. 4, 18(3): 57',234,'[216]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-04 06:09:48','admin'),(1360,'Leptolyngbya crispata','(Playfair) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1361',0,'active','2019-06-04 06:08:52','admin'),(1361,'Plectonema crispatum','Playfair 1915, Proc. Lin. Soc. N.S.W. 40: 350',273,'','','Species',NULL,'','','','pinky-brown stratum on a zinc-footwasher at the Presbyterian Church, Lismore district','',0,1,'',0,'active','2019-06-04 06:10:09','admin'),(1362,'Leptolyngbya crossbyana','(Tilden) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1363',0,'active','2019-06-04 06:09:00','admin'),(1363,'Phormidium crossbyanum','Tilden 1909',267,'[380]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-04 06:10:56','admin'),(1364,'Leptolyngbya dangeardii','(Frémy) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1365',0,'active','2019-06-04 06:09:13','admin'),(1365,'Plectonema dangeardii','Frémy 1930, Arch. Bot. Mém. 3(2): 175',273,'[221]','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>standing up to slightly flowing water</span></span>','[201]',0,1,'',0,'active','2019-06-04 06:10:14','admin'),(1366,'Leptolyngbya crassior','(Skuja) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1359',1,'active','2019-06-04 11:49:40','admin'),(1367,'Leptolyngbya desmidiacearum','(Noda) Umezaki &amp; Watanabe 1994, Jap. J. Phycol. 42: 204',225,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1368',0,'active','2019-06-04 11:51:36','admin'),(1368,'Plectonema desmidiacearum','Noda 1971, , J. Fac. Sci. Niigata Univ., ser. D (Biol.), no. 8: 61',273,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-04 12:01:13','admin'),(1369,'Schizothrix diplosiphon','(Voronichin) Anagnostidis 2001, Preslia 73: 368',300,'[9]','','Species',NULL,'[491]','','',NULL,NULL,0,1,'',0,'active','2019-06-04 12:03:55','admin'),(1370,'Leptolyngbya ectocarpi','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','','','',0,1,'clades:1371',0,'active','2019-06-04 11:50:18','admin'),(1371,'Phormidium ectocarpi','Gomont 1899, Bull. Soc. Bot. France 46: 37',267,'[224]','','Species',NULL,'','','','mud, <span lang=\'en\'><span title=\'\'>the coastal</span><span title=\'\'>&nbsp;regions of </span><span title=\'\'>England</span> <span title=\'\'>near </span><span title=\'\'>Plymouth</span></span>','[92]',0,1,'',0,'active','2019-06-04 11:52:48','admin'),(1372,'Leptolyngbya eliskae','Turicchia et al. 2009, Nova Hedwigia 89(1-2): 182',225,'[178]','iconotypus figura nostra 12 g-i','Species',NULL,'','BRNM 1454','3CC01S07','alkaline marshes','[95]',0,1,'',0,'active','2019-06-04 11:50:32','admin'),(1373,'Leptolyngbya elongata','(Thomas &amp; Gonzalves) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1374',0,'active','2019-06-04 11:50:48','admin'),(1374,'Phormidium africanum f. elongatum','Thomas &amp; Gonzalves 1965, Hydrobiologia 25:&nbsp;',267,'[381]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-04 11:52:40','admin'),(1375,'Leptolyngbya endophytica','Komárek 2004',225,'','???','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-04 12:08:08','admin'),(1376,'Pseudoscytonema endolithicum','(Ercegovic) Anagnostidis in Komárek &amp; Anagnostidis 2005, Suesswasserfl. Mitteleuropa 19/2: 546',286,'[31]','','Species',NULL,'[492]','','',NULL,NULL,0,1,'',1,'active','2019-08-08 07:55:14','admin'),(1377,'Leptolyngbya ercegovicii','(Čado) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1378',0,'active','2019-06-05 10:49:12','admin'),(1378,'Phormidium ercegovicii','Čado 1958, Zbornik Rabot. Filos. Fak. Univ. Skopje 5(21): 5',267,'[382]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-05 12:16:05','admin'),(1379,'Leptolyngbya erebi','(West &amp; G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[493]','','',NULL,NULL,0,1,'clades:1380',0,'active','2019-06-05 10:49:30','admin'),(1380,'Lyngbya erebi','West &amp; G.S.West 1911, Brit. Antarct. Exped. Vol. 1 Biology: 289',234,'[282]','','Species',NULL,'','','','in pond on Mt. Erebus','[2]',0,1,'',0,'active','2019-06-05 10:51:38','admin'),(1381,'Leptolyngbya fallax','(Hansgirg ex Forti) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1382',0,'active','2019-06-05 10:49:35','admin'),(1382,'Lyngbya fallax','Hansgirg 1891, &nbsp;Sitzungsber. Königl. Böhm. Ges. Wiss. Mat.-nat. Cl. 1: 348',234,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-05 10:51:48','admin'),(1383,'Leptolyngbya ferruginea','(G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1384',0,'active','2019-06-05 11:42:24','admin'),(1384,'Lyngbya ferruginea','&nbsp;G.S.West 1904, J. Bot. 42: 292',234,'[383]','','Species',NULL,'','','','freshwater, Roseau Valley','[18]',0,1,'',0,'active','2019-06-05 11:41:29','admin'),(1385,'Lyngbya fontana','Hansgirg 1892, Arch. naturwis. Landesdurchforsch. Böh. 8(4): 85.',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-05 13:05:49','admin'),(1386,'Leptolyngbya foveolarum','(Rabenhorst ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[495][494][496][497][498][499][500]','','',NULL,NULL,0,1,'clades:1387',0,'active','2019-06-05 13:04:53','admin'),(1387,'Phormidium foveolarum','Gomont 1892, Ann. Sci. &nbsp;Nat. Bot. ser. 7, 16: 164',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-05 13:00:49','admin'),(1388,'Aulosira laxa','Kirchner ex Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 256.',110,'','','Species',NULL,'','','NIES 50',NULL,NULL,1,1,'',0,'active','2019-06-05 12:58:23','admin'),(1389,'Wollea saccata','Bornet et Flahault 1888. Ann. Sci. Nat. Bot., ser. 7, 7: 223',344,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-05 12:56:51','admin'),(1390,'Leptolyngbya fragilis','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[501]','','',NULL,NULL,0,1,'clades:1391',0,'active','2019-06-05 13:04:27','admin'),(1391,'Phormidium fragile','Gomont 1892, Ann. Sci. NAt. Bot, ser. 7, 16: 163',267,'[235]','','Species',NULL,'','','','salt water','[60]',0,1,'',0,'active','2019-06-05 13:00:57','admin'),(1392,'Crocosphaera watsonii','Zehr, Rachel A.Foster, Waterbury et E.Webb in Mareš et al. 2019. Journal of Phycology 55: 601',140,NULL,NULL,'Species',NULL,NULL,'CBFS A-099-1','WH 8501','Open warm oligotrophic tropical ocean','',1,1,NULL,0,'active','2022-03-19 08:55:42','admin'),(1393,'Leptolyngbya frigida','(Fritsch) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[502]','','',NULL,NULL,0,1,'clades:1394',1,'active','2019-06-11 06:48:37','admin'),(1394,'Phormidium frigidum','Fritsch 1912, Nat. Antarct. &nbsp;Exped. 1901-04, 6(Freshw. Alg.): 29',267,'[384]','','Species',NULL,'','','','Dull brick-coloured ice, situated in long level line, as though in situation of former water-level. McMurdo Bay','[2]',0,1,'',0,'active','2019-06-05 13:32:49','admin'),(1395,'Leptolyngbya fritschiana','&nbsp;Komárek 2007, &nbsp;Polish Polar Res. 28(3): 221-224',1,'[375]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-06-05 13:24:16','admin'),(1396,'Ammatoidea normannii','W. et G.S. West, 1897. J. Roy. Microsc. Soc. London 1897: 506',101,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-05 14:04:02','admin'),(1397,'Tapinothrix bornetii','Sauvageau 1892. <em>Bulletin de la Société Botanique de France</em> 39: 123',328,'[385]','','Species',NULL,'','','','on submersed stones in running water','',1,1,'',0,'active','2019-06-05 14:05:14','admin'),(1398,'Anabaenopsis elenkinii','Miller 1923. Arch. Russk. Protistol. 2: 125',103,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-05 14:03:25','admin'),(1399,'Aphanizomenon flos-aquae','Ralfs ex Bornet et Flahault 1888',104,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 05:03:10','admin'),(1400,'Asterocapsa gloeotheceformis','Chu 1952. Ohio J. Sci. 52: (2): 97',109,'[386]','','Species',NULL,'','','','(Chu 1952) on wet surfaces of caves and rocks and cliffs under dripping water at<br>an altitude between 2000 and 3500 meters in Mt. Omei and Mt. Kingfu','[38]',1,1,'',0,'active','2019-06-06 12:44:16','admin'),(1401,'Baradlaia speluncaecola','Palik 1960',112,NULL,NULL,'Species',NULL,NULL,'','','in a cave','[65]',1,1,NULL,0,'active','2019-06-06 12:46:49','admin'),(1402,'Blennothrix vermicularis','&nbsp;(Kützing) Anagnostidis et Komárek 1988, Algolog. Stud. &nbsp;50-53: 430',113,'[102]','','Species',NULL,'[990][992][670][671]','','',NULL,NULL,1,1,'',0,'active','2020-04-07 07:38:34','admin'),(1403,'Borzia trilocularis','Cohn ex Gomont, 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 198.',114,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:47:50','admin'),(1404,'Brachytrichia quoyi','Bornet et Flahault 1887',116,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:48:29','admin'),(1405,'Brachytrichiopsis filiformis','Jao 1944. Sinensia 15:78',117,NULL,NULL,'Species',NULL,NULL,'','','dry limestone stones','[38]',1,1,NULL,0,'active','2019-06-06 12:50:32','admin'),(1406,'Camptylonemopsis lahorensis','(Ghose) Desikachary 1948',120,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:51:34','admin'),(1407,'Crinalium endophyticum','Crow 1927',139,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:52:23','admin'),(1408,'Leptolyngbya fritschii','Anagnostidis 2001, Preslia 73(4): 366',225,'[9]','nomen novum','Species',NULL,'','','',NULL,NULL,0,1,'clades:1409',0,'active','2019-06-06 12:57:47','admin'),(1409,'Plectonema notatum var. africanum','&nbsp;Fritsch &amp; Rich 1929, Trans. Roy. Soc. South Africa &nbsp;18: 90',273,'[387]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-06 12:56:05','admin'),(1410,'Leptolyngbya tenuissima','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[503]','','',NULL,NULL,0,1,'clades:1411',0,'active','2019-06-06 12:58:53','admin'),(1411,'Plectonema tenuissimum','Gardner 1927, Mem. N.Y. Bot. Gard. 7: 47-48',273,'[215]','type: no 1049b','Species',NULL,'','','','on the wall or a house in Maricao,&nbsp;','[26]',0,1,'',0,'active','2019-06-06 12:56:16','admin'),(1412,'Leptolyngbya gelatinosa','(Voronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1413',0,'active','2019-06-06 12:58:30','admin'),(1413,'Phormidium gelatinosum','Voronichin 1923, Bot. Mater. 2(7): 97',267,'[388]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-06 12:54:35','admin'),(1414,'Leptolyngbya gelatinicola','(Geitler) Anagnostidis 2001, Preslia 73(4): 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1415',0,'active','2019-06-06 12:58:19','admin'),(1415,'Phormidium gelatinicola','Geitler 1933, Arch. Hydrogiol. Suppl 12: 633',267,'[389]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-06 12:54:22','admin'),(1416,'Leptolyngbya geysericola','(Copeland) Anagnostidis 2001, Preslia 73(4): 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1417',0,'active','2019-06-06 12:58:40','admin'),(1417,'Phormidium geysericola','&nbsp;Copeland 1936, Ann. N.Y. Acad. Sci. 36: 186',267,'[374]','','Species',NULL,'','','','thermophilic, Riverside Geyser, Yellowstone Nat. Park','[113]',0,1,'',0,'active','2019-06-06 12:54:59','admin'),(1418,'Chlorogloea tuberculosa','(Hansgirg) Wille 1900',124,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:53:47','admin'),(1419,'Leptolyngbya glacialis','(West &amp; West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[504]','','',NULL,NULL,0,1,'clades:1422',0,'active','2019-06-06 12:58:47','admin'),(1420,'Alternantia serra','Schiller 1954',100,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 12:45:52','admin'),(1421,'Arthronema africanum','&nbsp;(Schwabe et Simonsen) Komárek et Lukavský 1988',107,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-12 04:17:57','admin'),(1422,'Phormidium glaciale','West &amp; West 1911, Brit. Ant. Exped. Vol. 1 Biol., p. 291',267,'[282]','','Species',NULL,'','','','freshwater, Blue Lake, Coast Lake, Clear Lake,','[2]',0,1,'',0,'active','2019-06-06 12:55:25','admin'),(1423,'Bacularia coerulescens','Borzì 1905. Nuova Notarisia 16: 21',111,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2022-03-22 13:54:46','admin'),(1424,'Desikacharya','Saraf, Dawda et P. Singh 2019. Notulae algarum 107',34,'[390][414]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-09-12 05:21:36','admin'),(1425,'Desikacharya nostocoides','Saraf, Dawda et P. Singh 2019. Notulae algarum 107',1424,'[390][414]','','Species',NULL,'','metabolically inactive strain GCC 20181','GCC 20181','seepage-dwelling cyanobacteria found to be growing as a mat having influence of both soil, a nearby small rocky shade and dripping water','[156]',1,1,'',0,'active','2019-09-12 05:22:01','admin'),(1426,'Desikacharya soli','Saraf, Dawda et P. Singh 2019. Notulae algarum 107',1424,'[390][414]','','Species',NULL,'','metabolically inactive strain GCC 20182','GCC 20182','typical soil-dwelling cyanobacteria which were found to be growing as a macroscopic mat','[156]',0,1,'',0,'active','2019-09-12 05:22:19','admin'),(1427,'Nostoc thermotolerans','Sudarkar, Villanueva, Gaysina, Casamatta, Saraf, Dighe, Mergu et P. Singh 2017. IJSEM 67: 1303',255,'[391]','','Species',NULL,'','inconotype Fig. 7.','MCC 3156','Soil-dwelling cyanobacteria which was found to be growing as a mat inside the crevices of a small hillock.','[156]',0,1,'',0,'active','2019-06-06 13:48:48','admin'),(1428,'Chamaecalyx swirenkoi','(Širšov) Komárek et Anagnostidis 1986. Algological Studies 38-39: 199',122,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 13:57:36','admin'),(1429,'Chlorogloeopsis fritschii','Mitra et Pandey 1967. Phykos 5',125,'','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-06-06 13:57:09','admin'),(1430,'Chamaesiphon confervicola','<em>Chamaesiphon confervicola</em> A. Braun in Rabenhorst 1865',123,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 14:12:56','admin'),(1431,'Chondrogloea africana','Schmidle 1901',126,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 14:12:44','admin'),(1432,'Chroococcidiopsis thermalis','Geitler 1933. Arch. Hydrobiol., Suppl. 12: 625.',660,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 14:14:36','admin'),(1433,'Chroococcopsis gigantea','Geitler, 1925. Arch. Protistenk. 51: 342.',129,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-06 14:27:04','admin'),(1434,'Clastidium setigerum','Kirchner 1880',132,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 04:18:00','admin'),(1435,'Colteronema funebre','Copeland 1936',138,'[374]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2020-01-13 15:29:26','admin'),(1436,'Coelomoron regularis','Buell 1938',134,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 04:00:47','admin'),(1437,'Coelosphaerium kuetzingianum','Nägeli 1849',422,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 08:40:28','admin'),(1438,'Cyanoarbor rupestris','Wang, 1989. Acta phytotax. sinica 27(2',143,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 04:02:15','admin'),(1439,'Cyanobacterium stanieri','Rippka et Cohen-Bazire 1983',144,'','does not meet ICN/ICNP rules for holotypes/type strains','Species',NULL,'','','PCC 7202',NULL,NULL,1,0,'',0,'active','2019-06-10 04:04:13','admin'),(1440,'Leptolyngbya gloeophila','(Borzì) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53:&nbsp;',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1441',0,'active','2019-06-10 04:06:35','admin'),(1441,'Plectonema gloeophilum','Borzì 1892, <em>Nuova Notarisia</em> 3: 40',273,'[392]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-10 04:09:23','admin'),(1442,'Leptolyngbya gloeophila 2','(Kützing ex Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','invalid name','Species',NULL,'','','',NULL,NULL,0,1,'clades:1443',0,'active','2019-06-10 04:07:13','admin'),(1443,'Lyngbya gloeophila','Kützing ex Hansgirg 1892: 87',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-10 04:05:36','admin'),(1444,'Pseudophormidium golenkinianum','(Gomont) Anagnostidis 2001, Preslia 73: 370',285,'[9]','','Species',NULL,'[505][507]','','',NULL,NULL,0,1,'clades:1445',0,'active','2019-06-10 04:08:51','admin'),(1445,'Plectonema golenkinianum','Gomont 1899, Bull. Soc. Bot. France 46: 35',273,'[224]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-10 04:09:47','admin'),(1446,'Leptolyngbya gracilis','(Lindstedt) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[508]','','',NULL,NULL,0,1,'clades:1447',0,'active','2019-06-10 04:07:23','admin'),(1447,'Phormidium gracile','Lindstedt 1943, &nbsp;Flora mar. Cyanoph. schwed. Westküste, p. 69',267,'[393]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-10 04:10:19','admin'),(1448,'Leptolyngbya gracillima','(Zopf ex Hansgirg) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53:391',225,'[102]','','Species',NULL,'[509][510][511]','','',NULL,NULL,0,1,'clades:1449',0,'active','2019-06-10 07:07:04','admin'),(1449,'Plectonema gracillimum','(Zopf) Hansgirg 1892, Arch. Naturwiss. Durchforsch. Böhmen 8 (4): 41',273,'[275]','','Species',NULL,'','','','','[54]',0,1,'',0,'active','2019-06-10 04:10:00','admin'),(1450,'Chroococcidium gelatinosum','Geitler 1933. Arch. Hydrobiol., Suppl. 12: 624.',128,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:12:13','admin'),(1451,'Coccopedia limnetica','Troickaja 1922',133,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:02:38','admin'),(1452,'Cyanobotrys lambinonii','L. Hoffman 1991. Arch. Hydrobiol./Alglological Studies 64',146,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2022-03-22 14:02:13','admin'),(1453,'Cyanocatena planctonica','Hindák 1975',663,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:05:59','admin'),(1454,'Cyanocomperia africana','Hindák 2001. Nova Hedwigia, Beih. 123: 81',149,NULL,NULL,'Species',NULL,NULL,'','','thermal spring','[207]',1,1,NULL,0,'active','2021-06-18 08:31:43','admin'),(1455,'Cyanocystis versicolor','Borzí 1882',150,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:07:21','admin'),(1456,'Cyanoderma bradypii','(Kuhn in Welcker) Weber van Bosse 1887',151,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:07:45','admin'),(1457,'Cyanodermatium gelatinosum','Geitler 1933',152,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:08:07','admin'),(1458,'Cyanodictyon endophyticum','Pascher 1914',153,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:08:37','admin'),(1459,'Cyanogranis basifixa','Hindák 1982. Arch. Hydrobiol./Algological Studies 32',397,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:06:46','admin'),(1460,'Cyanokybus venezuelae','Schiller 1956',155,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:09:03','admin'),(1461,'Cyanonephron styloides','Hickel 1985',156,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:09:29','admin'),(1462,'Cyanophanon mirabile','Geilter 1955',157,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:09:47','admin'),(1463,'Cyanostylon microcystoides','Geitler 1928',161,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:10:07','admin'),(1464,'Cyanotetras fusca','Hindák 1988',162,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-12 05:47:00','admin'),(1465,'Cyanothamnos plancticus','Cronberg 1991',163,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-10 13:10:58','admin'),(1466,'Cyanothece aeruginosa','(Nägeli) Komárek 1976. Archiv für Protistenkunde 118: 146',164,'[397]','','Species',NULL,'','Epitype CBFS A-103-1','SAG 87.79',NULL,NULL,1,1,'',0,'active','2020-04-16 08:27:07','admin'),(1467,'Cylindrospermum majus','Kützing ex Bornet et Flahault 1888',166,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 04:58:30','admin'),(1468,'Dalmatella buaensis','Ercegović 1929',1,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,1,'active','2019-06-10 13:05:42','admin'),(1469,'Dalmatella buaensis','Ercegović 1929',167,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:10:10','admin'),(1470,'Cryptococcum','Gama, Rigonato, Fiore et Sant Anna 2019. Eur. J. Phycol.',16,'[394]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-10 13:03:06','admin'),(1471,'Cryptococcum brasiliense','Gama, Rigonato, Fiore et Sant Anna 2019. Eur. J. Phycol.',1470,'[394]','','Species',NULL,'','SP 469754','CCIBt3410','growing on dry soil among pebbles','[172]',1,1,'',0,'active','2019-06-10 13:04:01','admin'),(1472,'Cryptococcum komarkovaum','Gama, Rigonato, Fiore et Sant Anna 2019. Eur. J. Phycol.',1470,'[394]','','Species',NULL,'','SP 469762','CCALA 054','aquatic, thermal spring','',0,1,'',0,'active','2019-06-10 13:04:10','admin'),(1473,'Inacoccus','Gama, Rigonato, Fiore et Sant Anna 2019. Eur. J. Phycol.',16,'[394]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-26 12:54:51','admin'),(1474,'Inacoccus carmineus','Gama, Rigonato, Fiore et Sant Anna 2019. Eur. J. Phycol.',1473,'[394]','','Species',NULL,'','SP 469755','CCIBt 3411','terrestrial, growing on rocks and concrete','[172]',1,1,'',0,'active','2019-07-26 12:55:01','admin'),(1475,'Leptolyngbya granulifera','(Copeland) Anagnostidis 2001, Preslia 73: 366',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1476',0,'active','2019-06-10 07:30:02','admin'),(1476,'Phormidium tenue var. granuliferum','Copeland 1936, Ann. N.Y. Acad. Sc.i 36: 178',267,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-10 07:29:21','admin'),(1477,'Leptolyngbya halophila','(Hansgirg) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[512][513][514]','','',NULL,NULL,0,1,'clades:1478',0,'active','2019-06-11 05:13:24','admin'),(1478,'Lyngbya halophila','Hansgirg ex Gomont 1892, Ann. Sci. Nat. Bot.,, ser. VII, &nbsp;16: 151',234,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-06-11 05:12:47','admin'),(1479,'Leptolyngbya hansgirgiana','&nbsp;Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','nomen novum','Species',NULL,'[515][516][517]','','',NULL,NULL,0,1,'',0,'active','2019-06-11 05:13:35','admin'),(1480,'Leptolyngbya hendersonii','(Howe) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1520',0,'active','2019-06-11 08:44:25','admin'),(1481,'Dasygloea amorpha','Berkeley ex Gomont 1892',168,NULL,NULL,'Species',NULL,'null[599]','','',NULL,NULL,1,1,NULL,0,'active','2019-08-29 13:04:35','admin'),(1482,'Dermocarpella hemisphaerica','Lemmermann, 1907. Bot. Jahrb. Syst. 38: 349',169,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 04:59:29','admin'),(1483,'Desmosiphon maculans','Borzi, 1907. Atti Congr. Nat. Ital. Milano 1906: 372.',170,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-12 06:05:30','admin'),(1484,'Dichothrix penicillata','Zanardini ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 3: 373',171,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:00:25','admin'),(1485,'Doliocatella formosa','Geitler, 1933. Arch. Hydrobiol., Suppl. 12: 630',173,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:01:36','admin'),(1486,'Dzensia salina','Voronichin, 1929. Izv. Glavn. Bot. Sada SSSR 28',174,'','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-06-11 05:02:04','admin'),(1487,'Entophysalis granulosa','Kützing 1843. Phycologia generalis: 177',175,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:02:31','admin'),(1488,'Epilithia adriatica','Ercegović 1932. Rad Jugoslav. Akad. Znan. 244: 141.',177,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:09:56','admin'),(1489,'Ercegovicia litoralis','(Ercegović) de Toni 1936',178,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:10:38','admin'),(1490,'Fischerella thermalis','Schwabe ex Gomont 1895',180,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:11:03','admin'),(1491,'Fischerellopsis harrisii','Fritsch 1932. J. Bot. 70',181,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:11:31','admin'),(1492,'Fortiea caucasica','(Elenkin) De Toni 1936',182,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:11:52','admin'),(1493,'Gardnerula corymbosa','(Harvey) De Toni 1936',183,NULL,NULL,'Species',NULL,'null[899][900]','','',NULL,NULL,1,1,NULL,0,'active','2020-03-27 11:07:45','admin'),(1494,'Geitleria calcarea','Friedmann 1955',184,'[488]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2020-01-14 16:26:52','admin'),(1495,'Geitleribactron periphyticum','Komárek 1975',185,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:53:22','admin'),(1496,'Glaucospira agilissima','Lagerheim 1892',188,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:53:44','admin'),(1497,'Gloeocapsa atrata','Kützing 1845',190,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:54:06','admin'),(1498,'Gloeotrichia pisum','Thuret ex Bornet et Flahault 1886',193,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:54:26','admin'),(1499,'Gomontiella subtubulosa','Teodoresco 1901',194,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:54:42','admin'),(1500,'Gomphosphaeriaceae','Elenkin',6,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-11 05:51:27','admin'),(1501,'Gomphosphaeria','Kützing 1836. Algarum Aquae Dulcis German. 16: 3.',1500,'','','Genus','[209]','',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-11 05:51:16','admin'),(1502,'Gomphosphaeria aponina','Kützing 1836',1501,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-11 05:51:11','admin'),(1503,'Halothece californica','Margheri, Ventura, Kaštovský et Komárek 2008',197,'[43]','','Species',NULL,'','BRNM HY1321','',NULL,NULL,1,1,'',0,'active','2019-06-13 05:53:12','admin'),(1504,'Handeliella stockmayeri','Skuja 1937',198,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:53:40','admin'),(1505,'Hapalosiphon pumillus','Kirchner ex Bornet et Flahault 1888',199,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:11:43','admin'),(1506,'Herpyzonema intermedium','Weber van Bosse 1913',201,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:55:56','admin'),(1507,'Heterocyanococcus haumanii','Kufferath 1929',202,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:59:01','admin'),(1508,'Heteroleibleinia rigidula','(Kützing ex Hansgirg) Hoffmann 1985',203,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:56:46','admin'),(1509,'Homoeoptyche repens','Skuja 1944',204,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:57:13','admin'),(1510,'Homoeothrix juliana','(Bornet et Flahault) Kirchner 1898',205,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:57:32','admin'),(1511,'Hormoscilla xishaensis','(Hua) Anagnostidis et Komárek 1988',207,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:58:33','admin'),(1512,'Hormathonema violaceo-nigrum','Ercegović 1930',206,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:58:07','admin'),(1513,'Hormothamnion enteromorphoides','Grunow ex Bornet et Flahault 1886',208,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:59:09','admin'),(1514,'Hormothece rupestris','Jao 1944',209,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 05:59:33','admin'),(1515,'Hydrococcus rivularis','Kützing 1833',210,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:00:07','admin'),(1516,'Hydrocoleum homoeotrichum','Kützing ex Gomont 1892, Ann. Sci. Nat. Bot. ser. 7, 15: &nbsp;344',211,'[145]','','Species',NULL,'[674][675][676][677][678][679][680]','','','freshwater, <span lang=\'en\'><span title=\'\'>rapidly</span><span title=\'\'>&nbsp;flowing</span><span title=\'\'>&nbsp;streams </span><span title=\'\'>and waterfalls</span></span> near Issoudun','[59]',1,1,'',0,'active','2019-12-04 12:26:07','admin'),(1517,'Hydrocoryne spongiosa','Schwabe ex Bornet et Flahault 1886',212,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:01:39','admin'),(1518,'Hyella caespitosa','Bornet et Flahault 1888',213,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:02:03','admin'),(1519,'Hyphomorpha antillarum','Borzì 1916',214,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:02:25','admin'),(1520,'Phormidium hendersonii','Howe 1918, Smithsonian Miscellaneous Collections 68(11): 2',267,'[395]','Types in herb. U. S. Nat. Museum and in herb. N. Y. Botanical Garden.','Species',NULL,'','','','On reef at Cayo Hutia (Jutias)','[16]',0,1,'',0,'active','2019-06-13 06:25:14','admin'),(1521,'Leptolyngbya henningsii','(Lemmermann) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1522',0,'active','2019-07-01 12:59:03','admin'),(1522,'Phormidium henningsii','Lemmermann 1910, Kryptogamenflora p. 124',267,'[378]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-01 13:02:22','admin'),(1523,'Isactis plana','Thuret ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 4',215,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:02:56','admin'),(1524,'Isocystis messanensis','Borzì ex Barnet et Flahault 1888',216,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:03:40','admin'),(1525,'Iyengariella tirupatiensis','Desikachary 1953',217,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:04:01','admin'),(1526,'Jaaginema subtilissimum','<em>Jaaginema subtilissimum</em> (Kützing ex De Toni) Anagnostidis et Komárek 1988',218,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:04:25','admin'),(1527,'Johannesbaptistia pellucida','(Dickie) Taylor et Drouet 1938',219,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:04:43','admin'),(1528,'Katagnymene pelagica','Lemmermann 1899',220,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:05:06','admin'),(1529,'Komvophoron schmidlei','(Jaag) Anagnostidis et Komárek 1988',221,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:05:38','admin'),(1530,'Leibleinia baculum','(Gomont) L. Hoffmann 1985',671,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:06:01','admin'),(1531,'Lithococcus ramosus','Ercegović 1925',402,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:09:56','admin'),(1532,'Lemmermanniella','Geitler 1942. In Engler et Prantl, Nat. Pflanzenfam., ed. 2, 1b: 62.',66,NULL,NULL,'Genus',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-06-13 06:07:54','admin'),(1533,'Lemmermanniella pallida','(Lemmermann) Geitler 1942',1532,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:07:06','admin'),(1534,'Lithomyxa calcigena','Howe 1931',231,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:09:15','admin'),(1535,'Loefgrenia anomala','Gomont 1896',232,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:10:22','admin'),(1536,'Loriella osteophila','Borzì 1892',233,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:10:41','admin'),(1537,'Lyngbya confervoides','C. Agardh ex Gomont 1892',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-12 05:07:37','admin'),(1538,'Lyngbyopsis willei','Gardner 1927, Mem. NY Bot. Gard. 7: 55',235,'[215]','','Species',NULL,'','','','on rocks in a brook, Utadao','[26]',1,1,'',0,'active','2019-11-15 13:36:26','admin'),(1539,'Mastigocladopsis jogensis','Iyengar et Desikachary 1946',238,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-12 05:36:55','admin'),(1540,'Mastigocladus laminosus','Cohn ex Kirchner 1898',239,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:11:51','admin'),(1541,'Mastigocoleopsis obtusa','(N. Carter) Geitler 1925',240,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:12:20','admin'),(1542,'Mastigocoleus testarum','Lagerheim ex Bornet et Flahault 1888',241,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:13:09','admin'),(1543,'Matteia conchicola','Borzì 1907',242,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-07-16 05:11:48','admin'),(1544,'Microcoleus vaginatus','Gomont &nbsp;ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 15: 355-356',245,'[145]','','Species',NULL,'[978][979][980][981][983][984][985][986][987][988][989]','','',NULL,NULL,1,1,'',0,'active','2020-04-07 07:13:49','admin'),(1545,'Microcrocis dietelii','Richer 1892',246,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:15:37','admin'),(1546,'Microcystis aeruginosa','(Kützing) Kützing 1846',247,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:16:01','admin'),(1547,'Merismopedia punctata','Meyen 1939',243,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:14:20','admin'),(1548,'Myxobaktron usterianum','Schmidle 1904',249,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:16:29','admin'),(1549,'Myxohyella socialis','(Setchell et Gardner) Geitler 1925',250,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:16:46','admin'),(1550,'Myxosarcina concinna','Printz 1921',251,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:17:01','admin'),(1551,'Nematoplaca incrustans','Geilter 1933',252,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:17:21','admin'),(1552,'Nephrococcus confertus','Li 1984',253,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:17:45','admin'),(1553,'Nodularia spumigena','Mertens ex Bornet et Flahault 1888',254,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:18:00','admin'),(1554,'Nostochopsis lobata','Wood ex Bornet et Flahault 1886',256,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-07-16 05:31:38','admin'),(1555,'Onkonema compactum','Geitler 1933',257,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:19:51','admin'),(1556,'Parenchymorpha xishanica','Tseng et Hua 1984',262,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 10:42:02','admin'),(1557,'Parthasarathilella prolifica','Subba Raju 1962',263,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:22:45','admin'),(1558,'Pascherinema moniliforme','(Pascher) de Toni 1936',264,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:23:03','admin'),(1559,'Phormidiochaete nordstedtii','(Bornet et Flahault) Komárek 2001',266,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:24:04','admin'),(1560,'Phormidium inundatum','Kützing ex Gomont 1892',267,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:25:50','admin'),(1561,'Pannus spumosus','Hickel 1991',260,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:20:08','admin'),(1562,'Cyanoplacoma vesiculosum','(Schousboe ex Bornet et Thuret) Molinari et Guiry 2021. Notulae Algarum 183: 3',19,'[621]','','Species',NULL,'','','',NULL,NULL,1,1,'',1,'active','2022-08-11 13:54:39','admin'),(1563,'Planktocyanocapsa stagnalis','Hindák 2002',269,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:26:47','admin'),(1564,'Planktolyngbya limnetica','(Lemmermann) Komárková-Legnerová et Cronberg 1992',668,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:27:07','admin'),(1565,'Podocapsa pedicellata','Ercegović 1931',275,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:27:27','admin'),(1566,'Polychlamydum insigne','West et G.S. West',276,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 06:27:47','admin'),(1567,'Porphyrosiphon notarisii','Kützing ex Gomont 1892',277,'[145]','','Species',NULL,'[610][611][612][613][614][615][616]','','','<span lang=\'en\'><span title=\'\'>bare ground, meadows, tree bark</span></span>','[69]',1,1,'',0,'active','2019-11-11 13:04:57','admin'),(1568,'Prochloron didemni','Lewin ex L. Hoffmann et Greuter 1996',279,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2020-05-25 11:26:55','admin'),(1569,'Aliterella shaanxiensis','Q. Zhang et L.R. Song 2019. Phytotaxa 374(3): 213',466,'[396]','','Species',NULL,'','HBI HZ 20130817','FACHB–2293','freshwater plankton','[38]',0,1,'',0,'active','2019-06-13 05:52:52','admin'),(1570,'Proterendothrix scolecoidea','West et G.S. West 1897',281,NULL,NULL,'Species',NULL,'null[694]','','',NULL,NULL,1,1,NULL,0,'active','2020-01-06 09:19:53','admin'),(1571,'Pseudanabaena catenata','Lauterborn 1915',282,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:23:58','admin'),(1572,'Pseudocapsa dubia','Ercegović 1925',283,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 08:00:20','admin'),(1573,'Pseudoncobyrsa lacustris','(Kirchner) Geitler 1925',284,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:28:24','admin'),(1574,'Pseudoscytonema malayense','(Biswas) Elenkin 1949, Monogr. Algarum, pars II,III, p. 1805',286,'[226]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1861',0,'active','2019-08-08 08:23:16','admin'),(1575,'Pulvinularia suecica','Borzì 1916',287,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-07-16 05:39:27','admin'),(1576,'Radaisia gomontiana','Sauvageau 1892',288,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:29:49','admin'),(1577,'Radiocystis geminata','Skuja 1948',289,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:30:15','admin'),(1578,'Raphidiopsis curvata','Fritsch et Rich 1929',290,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:30:42','admin'),(1579,'Rhabdoderma lineare','Schmidle et Lauterborn 1900',292,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:22:55','admin'),(1580,'Rhabdogloea ellipsoidea','Schröder 1917',293,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:23:04','admin'),(1581,'Rhodostichus expansus','Geitler et Pascher in Geitler 1931',294,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:35:11','admin'),(1582,'Richelia intracellularis','&nbsp;Johnson Schmidt 1901',295,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:35:31','admin'),(1583,'Rivularia atra','Roth ex Bornet et Flahault 1886. Ann. Sci. Nat. Bot., ser. 7, 4: 353',296,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:33:43','admin'),(1584,'Rubidibacter lacunae','Choi, Noh, Lee et Rho 2008. Int. J. of Systematic and Evolutionary Microbiology 58: 2811',298,'[47]','','Species',NULL,'','','UTEX L2944','','[131]',1,1,'',0,'active','2021-06-18 08:07:29','admin'),(1585,'Sacconema rupestre','Borzi ex Bornet et Flahault, 1886. Ann. Sci. Nat. Bot., ser. 7, 3: 381',299,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:34:00','admin'),(1586,'Schmidleinema indicum','(Schmidle) De Toni 1936',301,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:36:40','admin'),(1587,'Scytonema hofmanni','Agardh ex Bornet et Flahault 1887. Ann. Sci. Nat. Bot., ser. 7, 5: 97',302,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:34:47','admin'),(1588,'Scytonamatopsis woronichinii','Kiseleva 1930',303,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:34:35','admin'),(1589,'Seguenzaea sicula','Borzì 1907',304,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:36:16','admin'),(1590,'Sinaiella terricola','Gruia 1965',305,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:37:02','admin'),(1591,'Siphononema polonicum','(Raciborski) Geitler 1925',306,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:37:28','admin'),(1592,'Siphonosphaera pannonica','Hindák 1988',423,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:37:47','admin'),(1593,'Sirocoleum guyanense','Kützing ex Gomont 1892. Ann. Sci. Nat. Bot., ser. 7, 15: 348',308,'[145]','','Species','','','','','sea- shore','',1,1,'',0,'active','2019-08-29 11:54:22','admin'),(1594,'Snowella rosea','(Snow) Elenkin 1938',424,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:38:27','admin'),(1595,'Sokolovia neumaniae','Elenkin 1926',310,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2023-01-31 08:34:40','admin'),(1596,'Solentia stratosa','Ercegović 1927',311,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:39:08','admin'),(1597,'Spelaeopogon sommieri','Borzì 1907',312,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:40:02','admin'),(1598,'Sphaerocavum brasiliense','<em>&nbsp;</em>Azevedo et Sant\' Anna 2003',313,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:40:20','admin'),(1599,'Stanieria cyanosphaera','(Komárek et Hindák) Komárek et Anagnostidis 1986',317,NULL,NULL,'Species',NULL,NULL,'','Hindák 1965/25 = PCC 7347',NULL,NULL,1,1,NULL,0,'active','2020-05-04 05:56:53','admin'),(1600,'Starria zimbabweensis','Lang 1977. J. Phycol. 13: 289',318,NULL,NULL,'Species',NULL,NULL,'','SAG 74.90 = UTEX 1754',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:40:53','admin'),(1601,'Stauromatonema viride','Frémy 1930',319,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:41:11','admin'),(1602,'Stichosiphon regularis','Geitler 1932',320,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:41:28','admin'),(1603,'Symphyonema sinense','Jao 1944. Sinensia 15: 81',322,'[450]','','Species',NULL,'','','',NULL,NULL,1,1,'',0,'active','2019-10-08 04:53:31','admin'),(1604,'Symphyonemopsis katriensis','Tiwari et Mitra 1969',323,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:42:06','admin'),(1605,'Symplocastrum friesii','(Agardh) Kirchner 1900, Schizophyceae, p. 68',325,'[491]','','Species',NULL,'[724][725][726][728][729][730][731][732]','','','terram nudam, vias silvaticas umbrosas, rupes madidas et muscosas, etiam stillicidia et locos inundatos','',1,1,'',0,'active','2020-02-17 12:57:11','admin'),(1606,'Synechococcus elongatus','(Nägeli) Nägeli 1849',326,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:22:04','admin'),(1607,'Synechococcus elongatus','(Nägeli) Nägeli 1849',1,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,1,'active','2019-06-14 04:43:10','admin'),(1608,'Synechocystis aquatilis','Sauvageau 1892',327,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:43:42','admin'),(1609,'Thalpophila cossyrensis','Borzì 1907',329,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:43:56','admin'),(1610,'Thiochaete chutteri','Welsh 1961',331,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 11:37:29','admin'),(1611,'Trichocoleus delicatulus','(West et G.S.West) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:2117',0,'active','2020-03-27 13:27:38','admin'),(1612,'Trichodesmium erythraeum','Ehrenberg ex Gomont 1892, Ann. Sci. Nat. Bot., Sér. 7, 16: 196',334,'[235]','','Species',NULL,'[697][698][699][700]','','','marine, Red Sea, Indian Ocean, near&nbsp; Zanzibar','[232]',1,1,'',0,'active','2020-01-08 14:11:23','admin'),(1613,'Trichormus variabilis','(Kützing ex Bornet et Flahault) Komárek et Anagnostidis 1987',335,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 11:35:47','admin'),(1614,'Tryponema endolithicum','Ercegović 1925',336,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-13 11:40:59','admin'),(1615,'Tubiella elenkinii','Hollerbach 1934',337,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 04:21:04','admin'),(1616,'Prochlorothrix hollandica','Burger-Wiersma, Stall et Mur 1989',280,NULL,NULL,'Species',NULL,NULL,'','PCC 9006',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:07:32','admin'),(1617,'Cylindrospermopsis raciborskii','(Woloszynska) Subba Raju 1972. Taxonomy and Biology of Blue-green Algae, 1.Int. Symp. Tax. Biol. Blue-green Algae, Madras, p. 55',165,'','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1793',0,'active','2019-07-25 11:43:19','admin'),(1618,'Cyanobium gracile','Rippka et Cohen-Bazire 1983',145,'','type not specified (does not meet requirements of ICN nor ICNP)','Species',NULL,'','','PCC 6307',NULL,NULL,1,0,'',0,'active','2021-05-28 06:36:09','admin'),(1619,'Umezakia natans','M. Watanabe 1987',339,NULL,NULL,'Species',NULL,NULL,'','NIES-2665',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:07:46','admin'),(1620,'Voukiella rupestris','Ercegović 1925',340,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:08:02','admin'),(1621,'Westiella intricata','Borzì 1907',341,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:08:17','admin'),(1622,'Westiellopsis prolifica','Janet 1941',342,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:08:35','admin'),(1623,'Wolskyella filamentosa','Claus 1963',345,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:06:36','admin'),(1624,'Woronichinia naegeliana','(Unger) Elenkin 1933',425,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:06:11','admin'),(1625,'Xenococcus schousboei','Thuret 1875',347,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:05:13','admin'),(1626,'Xenotholos huastecanus','Gold-Morgan, Montejano et Komárek 1994',348,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:05:23','admin'),(1627,'Yonedaella lithophytica','(Ercegović) Umezaki 1962',349,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-06-14 05:04:47','admin'),(1628,'Zehria','Johansen et Mareš 2019. Journal of Phycology 55: 603',21,'[397]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 14:18:25','admin'),(1629,'Zehria floridana','Johansen et Mareš 2019. Journal of Phycology 55: 603',1628,NULL,NULL,'Species',NULL,NULL,'CBFS A-100-1','WH 8904',NULL,NULL,1,1,NULL,0,'active','2019-07-30 09:29:43','admin'),(1630,'Lusitaniella','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 25',2556,'[129]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 13:24:33','admin'),(1631,'Lusitaniella coriacea','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 25',1630,'[129]','','Species',NULL,'','CBFS A074-2','LEGE 07167','epilithic mats, on the surface of (immersed) rocks or in tide puddles','[82]',1,1,'',0,'active','2019-06-14 11:03:51','admin'),(1632,'Jaaginema litorale','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 26',218,'[129]','','Species',NULL,'','CBFS A-076-1','LEGE 07176','epilithic on wave-exposed rocks in intertidal zones','[82]',0,1,'',0,'active','2019-06-14 11:04:18','admin'),(1633,'Calenema','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 29',1034,'[129]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:18:29','admin'),(1634,'Calenema singularis','Ramos, Brito et Kaštovský 2017. Molecular Phylogenetics and Evolution 111: 30',1633,'[129]','','Species',NULL,'','CBFS A-072-1','LEGE 06188','coastal sea water in surf zone','[82]',1,1,'',0,'active','2019-06-14 13:00:59','admin'),(1635,'Odorella','Shalygin, Huang, Allen, Burkholder et Zimba 2019. Journal of Phycology 55: 511',2557,'[398]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:29:35','admin'),(1636,'Odorella benthonica','Shalygin, Zimba et Huang 2019. Journal of Phycology 55:511',1635,'[398]','','Species',NULL,'','PH 00179868','CCALA 10281','benthos in an aqueduct','[113]',1,1,'',0,'active','2019-08-14 04:53:18','admin'),(1637,'Trichodesmium brasiliense','Sant Anna, Gama, Silva et Vieira 2018. Rodriguésia 69(4): 2021',334,'[399]','','Species',NULL,'','SP469314','','pond, presence of macrophytes','[172]',0,1,'',0,'active','2019-06-14 13:01:43','admin'),(1638,'Desertifilum dzianense','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard 2018. FEMS Microbiology Ecology 94(8)',486,'[400]','','Species',NULL,'','cryopreserved strain PMC 872.14','PMC 872.14','stromatolites, saline-alkaline environment','[215]',0,1,'',0,'active','2019-06-14 13:48:40','admin'),(1639,'Sodalinema','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard 2018. FEMS Microbiology Ecology 94(8)',50,'[400][586]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-08-27 12:44:33','admin'),(1640,'Sodalinema komarekii','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard 2018. FEMS Microbiology Ecology 94(8)',1639,'[400]','','Species',NULL,'','cryopreserved strain PMC 869.14','PMC 869.14','water column and stromatolites, salinealkaline environment','[215]',1,1,'',0,'active','2019-06-14 13:48:06','admin'),(1641,'Sodaleptolyngbya','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard 2018. FEMS Microbiology Ecology 94(8)',1034,'[400]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:27:10','admin'),(1642,'Sodaleptolyngbya stromatolitii','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard 2018. FEMS Microbiology Ecology 94(8)',1641,'[400]','','Species',NULL,'','cryopreserved strain PMC 867.14','PMC 867.14','stromatolites, saline-alkaline environment','[215]',1,1,'',0,'active','2019-06-14 14:04:51','admin'),(1643,'Haloleptolyngbya elongata','M. Cellamare, C. Duval, N. Touibi, C. Djediat et C. Bernard',444,'[400]','','Species',NULL,'','cryopreserved strain PMC 893.15','PMC 893.15','water column, saline-alkaline environment','[215]',0,1,'',0,'active','2019-06-14 14:05:33','admin'),(1644,'Minunostoc','F. Cai et R. Li 2019. Fottea 19(1): 14',34,'[402]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2019-06-20 05:56:24','admin'),(1645,'Minunostoc cylindricum','F. Cai et R. Li 2019. Fottea 19(1): 15',1644,'[402]','ambiguous holotype designation','Species',NULL,'','','','wet rocky wall','[38]',1,0,'',0,'active','2019-06-20 05:56:11','admin'),(1646,'Compactonostoc','F. Cai et R. Li 2019. Notulae Algarum 121',34,'[401][544]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-05-14 12:37:55','admin'),(1647,'Compactonostoc shennongjiaensis','F. Cai et R. Li 2019. Notulae algarum 121',1646,'[401][544]','','Species',NULL,'','HBI SNJ201101','CHAB5781','rocky walls in cold region','[38]',1,1,'',0,'active','2020-05-14 12:38:57','admin'),(1648,'Lagosinema','Akagha et Johansen 2019. Fottea 19(1): 3',2546,'[403]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:13:47','admin'),(1649,'Lagosinema tenuis','Akagha et Johansen 2019. Fottea 19(1): 4',1648,'[403]','','Species',NULL,'','BRY37768','NGPC151','brackish water','[219]',1,1,'',0,'active','2019-06-27 08:03:12','admin'),(1650,'Myxacorys','Pietrasiak et Johansen 2019. Journal of Phycology 55: 980',61,'[404]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-12-05 14:40:38','admin'),(1651,'Myxacorys chilensis','Pietrasiak et Johansen 2019. Journal of Phycology',1650,'[404]','','Species',NULL,'','NMC 86485','ATA2-1-KO14','soil crust on fine sand','[178]',1,1,'',0,'active','2019-06-27 11:50:22','admin'),(1652,'Myxacorys californica','soil crust on fine sand',1650,'[404]','','Species',NULL,'','NMC 86516','WJT36-NPBG1','biological soil crust on coarse granitic sandy soil','[113]',0,1,'',0,'active','2019-06-27 11:50:15','admin'),(1653,'Leptothoe','Konstantinou et Gkelis 2019. Journal of Phycology',2545,'[405]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:36:05','admin'),(1654,'Leptothoe sithoniana','Konstantinou et Gkelis 2019. Journal of Phycology',1653,'[405]','','Species',NULL,'','ΤAU A01001','TAU-MAC 0915','rocky reef of the sublittoral zone; found to live in association with the sponge Petrosia ficiformis at a depth of 19.5 m','[62]',1,1,'',0,'active','2019-07-01 10:57:05','admin'),(1655,'Leptothoe kymatousa','Konstantinou et Gkelis 2019. Journal of Phycology',1653,'[405]','','Species',NULL,'','TAU A01002','TAU-MAC 1215','rocky reef of the sublittoral zone; found to live in association with the sponge <em>Chondrilla nucula</em> at a depth of 9.6 m','[62]',0,1,'',0,'active','2019-07-01 10:57:20','admin'),(1656,'Leptothoe spongobia','Konstantinou et Gkelis 2019. Journal of Phycology',1653,'[405]','','Species',NULL,'','TAU A01003','TAU-MAC 1015','rocky sublittoral zone; found to live in association with the sponges <em>Acanthella acuta</em> and<em> Dysidea avara</em> at depths of 9.6 and 19.5 m','[62]',0,1,'',0,'active','2019-07-01 10:57:13','admin'),(1657,'Leptolyngya homogenea','(Gerdner) Anagnostidis 2001',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1658',0,'active','2019-07-02 10:35:51','admin'),(1658,'Phormidium purpurascens var. homogeneum','Gardner 1927, Mem. New York Bot. Garden 7: 45',267,'[215]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-02 10:36:55','admin'),(1659,'Leptolyngbya hormoides','(Setchell et Gardner) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1660',0,'active','2019-07-02 12:07:18','admin'),(1660,'Phormidium hormoides','Setchell &amp; Gardner in Gardner 1918, Univ. Calif. Publ. Bot. 6 (17): 467',267,'[406]','Physiological Laboratory, University of California, Berkeley, 1905. Type no. 1535, Gardner','Species',NULL,'','','','on glass aquaria of salt water from Pacific Ocean, California, Berkeley','[113]',0,1,'',0,'active','2019-07-03 10:39:43','admin'),(1661,'Leptolyngbya hypolimnetica','(Campbell) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1662',0,'active','2019-07-03 10:35:41','admin'),(1662,'Phormidium hypolimneticum','Campbell 1985, Algolog. Stud. 38/39: 184',267,'[407]','type of the culture - PCC Paris, Heinz Steinitz Marine Biology Laboratory, Elat, Israel','Species',NULL,'','','','hypolimnion of the Solar Lake, Sinai','[105]',0,1,'',0,'active','2019-07-03 10:41:07','admin'),(1663,'Leptolyngbya indica','',1,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,1,'active','2019-07-03 10:59:11','admin'),(1664,'Leptolyngbya jadertina','(Kützing ex Hansgirg) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'[520][522][524]','','',NULL,NULL,0,1,'synonyms:523',0,'active','2019-07-09 08:42:50','admin'),(1665,'Leptolyngbya komarovii','(Anissimova) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1666',0,'active','2019-07-10 06:15:03','admin'),(1666,'Phormidium komarovii','Anissimova in Elenkin 1949, Monogr. Cyanoph. 2, p. 1468',267,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-10 06:15:37','admin'),(1667,'Leptolyngbya lagerheimii','(Gomont ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391',225,'[102]','','Species',NULL,'[525][526][527][528]','','',NULL,NULL,0,1,'clades:1668',0,'active','2019-07-10 08:24:40','admin'),(1668,'Lyngbya lagerheimii','Gomont ex Gomont 1892, Ann. Sci. Nat., série 7, ​Botanique 16: 147',234,'[235]','','Species',NULL,'','','','lagoon Rodrigo de Freitas, Rio de Janeiro','[172]',0,1,'',0,'active','2019-07-10 08:01:30','admin'),(1669,'Lyngbya aestuarii','Liebman ex Gomont 1892',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-10 08:01:16','admin'),(1670,'Leptolyngbya laminosa','(Gomont ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[529][530][531][532]','','',NULL,NULL,0,1,'clades:1671',0,'active','2019-07-10 13:26:58','admin'),(1671,'Phormidium laminosum','Gomont ex Gomont 1892, Ann. Sci. Nat., serie 7 Bot. 16: 167',267,'[235]','','Species',NULL,'','','','thermal water','',0,1,'',0,'active','2019-07-10 13:28:08','admin'),(1672,'Leptolyngbya lapidea','(Geitler) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1673',0,'active','2019-07-10 13:27:12','admin'),(1673,'Phormidium lapideum','Geitler 1933, Arch. Hydrobiol. Suppl. 12: 633',267,'[389]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-10 13:28:14','admin'),(1674,'Leptolyngbya leptotrichiformis','(Krieger) Anagnostidis &amp; Komárek in Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1675',0,'active','2019-07-10 13:27:25','admin'),(1675,'Lyngbya leptotrichiformis','Krieger 1944, Ber. Dtsch. Bot. Ges. 61(5): 257',234,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-10 13:27:46','admin'),(1676,'Leptolyngbya lignicola','(Frémy) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1677',0,'active','2019-07-11 08:03:50','admin'),(1677,'Phormidium lignicola','Frémy 1930, Arch. Bot. Mem. 3(2): 142',267,'[221]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-11 08:03:35','admin'),(1678,'Leptolyngbya maior','(Claus) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1679',0,'active','2019-07-11 13:18:49','admin'),(1679,'Phormidium fragile f. maius','Claus 1962, Nova Hedwigia 4: 69',267,'[409]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-11 08:03:23','admin'),(1680,'Leptolyngbya margaretheana','&nbsp;(Schmid) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1681',0,'active','2019-07-11 11:31:45','admin'),(1681,'Lyngbya margaretheana','Schmidt 1914, Ber. Dtsch. Bot. Ges. 32: 128',234,'[410]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-11 11:31:08','admin'),(1682,'Leptolyngbya margaritata','(Kufferath) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1683',0,'active','2019-07-11 11:31:55','admin'),(1683,'Lyngbya margaritata','Kufferath 1929, Ann. Crypt. Exot. 2: 48-49',234,'[411]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-11 11:31:21','admin'),(1684,'Leptolyngbya marina','(Gardner) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1685',0,'active','2019-07-11 13:31:13','admin'),(1685,'Phormidium tenue var. marinum','Gardner 1932, Sci. Surv. Porto Rico 8(2): 282',267,'[412]','','Species',NULL,'','','','forming thin layers on sand rock in the lower littoral belt','[26]',0,1,'',0,'active','2019-07-11 13:29:48','admin'),(1686,'Leptolyngbya membraniporae','(Lindstedt) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1687',0,'active','2019-07-11 13:31:21','admin'),(1687,'Lyngbya membraniporae','Lindstedt 1943',234,'[393]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-11 13:30:05','admin'),(1688,'Phormidium scytonematicola var. minus','Gardner 1927',267,'[215]','','Species',NULL,'','','','on rocks','[26]',0,1,'',0,'active','2019-07-11 13:29:39','admin'),(1689,'Leptolyngbya minor','(Gardner) Anagnostidis 2001, Preslia 73: 369',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1688',0,'active','2019-07-11 13:31:27','admin'),(1690,'Leptolyngbya minuta','(Lindstedt) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53:392',225,'[102]','','Species',NULL,'[533]','','',NULL,NULL,0,1,'clades:1691',0,'active','2019-07-12 09:59:43','admin'),(1691,'Phormidium minutum','Lindstedt 1943, Flora mar. Cyanoph. schwed. Westküste, p. 68',267,'[393]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-12 09:58:29','admin'),(1692,'Leptolyngbya minutissima','(Kufferath) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'[534]','','',NULL,NULL,0,1,'clades:1693',0,'active','2019-07-12 09:59:54','admin'),(1693,'Lyngbya minutissima','Kufferath 1929, Ann. Crypt. Exot. 2(1): 48',234,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-12 09:59:13','admin'),(1694,'Leptolyngbya mucicola','&nbsp;(Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[535]','','',NULL,NULL,0,1,'',0,'active','2019-07-12 10:00:03','admin'),(1695,'Lyngbya mucicola','Lemmermann 1904, Ark. Bot. 2(2): 70',234,'[413]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-12 09:59:24','admin'),(1696,'Leptolyngbya mucosa','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1697',0,'active','2019-07-12 10:00:07','admin'),(1697,'Phormidium mucosum','Gardner 1927, Mem. N.Y. Bot. Gard. 7: 43',267,'[215]','','Species',NULL,'','','','basin in a garden in Humacao','[26]',0,1,'',0,'active','2019-07-12 09:58:41','admin'),(1698,'Desikacharya thermotolerans','(Sudkar et al.) Saraf et P. Singh 2019. Notulae algarum 107',1424,'[414]','','Species',NULL,'','','MCC 3156',NULL,NULL,0,1,'clades:1427',0,'active','2019-09-12 05:24:09','admin'),(1699,'Anabaena oscillarioides','Bory ex Bornet et Flahault 1888',102,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,1,1,NULL,0,'active','2019-07-16 08:52:42','admin'),(1700,'Stigonema dinghuense','Song et Li 2015. Phytotaxa 213(3): 214',321,'[415]','','Species',NULL,'','CHCB DH-2013012030-1','','Wet rocky walls in the temperate region.','[38]',0,1,'',0,'active','2019-07-16 10:42:22','admin'),(1701,'Leptolyngbya muralis','(Gardner) Anagnostidis &amp; Komárek 1988',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1702',0,'active','2019-07-17 10:48:12','admin'),(1702,'Plectonema murale','Gardner 1927, Mem. N.Y. Bot. Gard. 7: 47',273,'[215]','type no 732 c','Species',NULL,'','','','on the wall of a bridge, Juan Martin, Fajardo','[26]',0,1,'',0,'active','2019-07-17 10:46:55','admin'),(1703,'Leptolyngbya mycoidea','(Frémy) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1704',0,'active','2019-07-17 10:48:19','admin'),(1704,'Phormidium mycoideum','&nbsp;Frémy in Feldmann 1935, Notes Stat. Ocennogr. Salammbo (Tunis) 29: 7',267,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-17 10:47:13','admin'),(1705,'Leptolyngbya nana','(Tilden) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1706',0,'active','2019-07-17 11:33:30','admin'),(1706,'Lyngbya nana','Tilden 1896, Amer. Alg. 2: 179',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-17 10:47:33','admin'),(1707,'Leptolyngbya norvegica','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1710',0,'active','2019-07-17 11:44:02','admin'),(1708,'Leptolyngbya nigrescens','Komárek 2007, Polish Poalr Res. 28(3): 221',1,'[375]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-07-17 11:03:53','admin'),(1709,'Leptolyngbya nodulosa','Li &amp; J.Brand 2007,&nbsp;',1,'','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-07-17 11:25:23','admin'),(1710,'Plectonema norvegicum','Gomont 1899, Bull. Soc. Bot. France 46: 34',273,'[224]','','Species',NULL,'','','','marine','[80]',0,1,'',0,'active','2019-07-19 08:17:12','admin'),(1711,'Leptolyngbya nostochoides','(Jao) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1712',0,'active','2019-07-19 08:18:29','admin'),(1712,'Phormidium nostochoides','Jao 1948, Bot. Bull. Acad. Sin. 2: 169',267,'[416]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 08:16:53','admin'),(1713,'Cyanomargaritaceae','Shalygin et al. 2017',9,'[170]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-07-19 12:00:14','admin'),(1714,'Leptolyngbya nostocorum','(Bornet ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[538]','','',NULL,NULL,0,1,'clades:1715',0,'active','2019-07-19 11:09:24','admin'),(1715,'Plectonema nostocorum','&nbsp;Bornet ex Gomont 1892, Ann. Sci. Nat., Bot. 7, 16: 102',273,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 11:08:54','admin'),(1716,'Leptolyngbya notata','&nbsp;(Schmidle) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1717',0,'active','2019-07-19 11:09:31','admin'),(1717,'Plectonema notatum','Schmidle in Simmer 1901, Allg. Bot. Ztschr. 7: 84-85',273,'[417]','','Species',NULL,'','','','1500 m a s','[49]',0,1,'',0,'active','2019-07-19 11:09:01','admin'),(1718,'Leptolyngbya ochracea','(Thuret ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1719',0,'active','2019-07-23 04:07:43','admin'),(1719,'Lyngbya ochracea','Thuret ex Gomont 1892, Ann. Sci. Nat. Bot. 7, 16: 149',234,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 12:02:10','admin'),(1720,'Leptolyngbya ochridana','(Čado) Anagnostidis &amp; Komárek 2001, Preslia 73: 367',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1721',0,'active','2019-07-19 12:00:57','admin'),(1721,'Phormidium gelatinosum f. ochridanum','Čado 1958, Zborn. Rab. Filoz. Fak. Univ. Skopje, Hidrob. Zav., OSchrid, 5(21): 40',267,'[382]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 12:02:58','admin'),(1722,'Leptolyngbya olivacea','(Kützing ex Hansgirg) Anagnostidis 2001, Preslia 73: 367',225,'[102]','','Species',NULL,'[539][540]','','',NULL,NULL,0,1,'clades:1723',0,'active','2019-07-19 12:01:05','admin'),(1723,'Lyngbya olivacea','Kützing ex Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 87',234,'[275]','','Species',NULL,'','','','freshwater','',0,1,'',0,'active','2019-07-19 12:02:35','admin'),(1724,'Leptolyngbya orientalis','(G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[541][542]','','',NULL,NULL,0,1,'clades:1725',0,'active','2019-07-19 12:15:15','admin'),(1725,'Phormidium orientale','&nbsp;G.S.West 1902, J. Bot. 40: 248',267,'[418]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 12:03:07','admin'),(1726,'Leptolyngbya patinae','(Schwabe) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1727',0,'active','2019-07-19 13:08:57','admin'),(1727,'Lyngbya patinae','Schwabe 1944, Mitt. deutsch. Ges. Nat.- Völker. Ostasiens Suppl. 21: 180',234,'[371]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 13:08:25','admin'),(1728,'Leptolyngbya perelegans','(Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1729',0,'active','2019-07-19 13:09:04','admin'),(1729,'Lyngbya perelegans','&nbsp;Lemmermann 1899,&nbsp;',234,'[95]','','Species',NULL,'','','','Laysan','[113]',0,1,'',0,'active','2019-07-19 13:08:33','admin'),(1730,'Leptolyngbya perforans','(Geitler) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[544][545]','','',NULL,NULL,0,1,'clades:1731',0,'active','2019-07-19 13:34:06','admin'),(1731,'Schizothrix perforans','Geitler 1928, Arch. Protistenk. 60(2): 446',300,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 13:33:07','admin'),(1732,'Leptolyngbya phormidioides','(Anagnostidis) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1733',0,'active','2019-07-19 13:34:13','admin'),(1733,'Oscillatoria acuminata f. phormidioides','Anagnostidis 1961, Untersuch. Cyanophyceen, p. 233',258,'[419]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-19 13:33:39','admin'),(1734,'Plectonema polymorphum','Schwabe 1960, Nova Hedwigia 2(1-2): 25',273,'[376]','','Species',NULL,'[546]','','',NULL,NULL,0,1,'',0,'active','2019-07-23 04:13:41','admin'),(1735,'Leptolyngbya polymorpha','(Schwabe) Anagnostidis 2001, Preslia 73: 367',1,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-07-22 10:14:22','admin'),(1736,'Leptolyngbya polysiphoniae','(Frémy) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'[547]','','',NULL,NULL,0,1,'clades:1737',0,'active','2019-07-23 04:14:30','admin'),(1737,'Lyngbya polysiphoniae','Frémy 1930, Arch. Bot., Mém. 3(2): 194',234,'[221]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 04:12:39','admin'),(1738,'Leptolyngbya protospira','(Skuja) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1739',0,'active','2019-07-23 04:14:38','admin'),(1739,'Lyngbya protospira','<em>Skuja 1939, </em>Acta Horti Botanici Universitatis Latviensis 11/12: 50',234,'[420]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 04:13:01','admin'),(1740,'Leptolyngbya pseudotenuis','(Stockmayer &amp; Skuja) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1742',0,'active','2019-07-23 11:16:31','admin'),(1741,'Rivularia halophila','Shalygin et Pietrasiak 2018. European Journal of Phycology 53(4): 539',296,'[421]','','Species',NULL,'','NMC865010','PUNA-NP3 = CCALA 1120 = CCMP 3497','situated in hyperarid environment, attached to the substrate, close to the air-water interface among precipitated salt crystals','[170]',0,1,'',0,'active','2019-07-23 06:49:06','admin'),(1742,'Phormidium pseudotenue','Stockmayer &amp; Skuja in Skuja 1937, Symbolae Sinicae p. 39',267,'[422]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 12:11:00','admin'),(1743,'Leptolyngbya pseudotenuis','(Stockmayer &amp; Skuja) Anagnostidis 2001, Preslia 73: 367',1,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1742',1,'active','2019-07-23 11:16:00','admin'),(1744,'Leptolyngbya pseudovalderiana','&nbsp;(Voronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[548]','','',NULL,NULL,0,1,'clades:1745',0,'active','2019-07-23 12:11:19','admin'),(1745,'Phormidium pseudovalderianum','Voronichin 1930, Tr. Leningr. Obšč. Estestv. 60(3): 68',267,'[423]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 12:10:42','admin'),(1746,'Phormidium purpurascens','Gomont ex Gomont<em>&nbsp;</em>1892, Ann. Sci. Nat., Bot. 7, &nbsp;16: 166',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 12:10:29','admin'),(1747,'Leptolyngbya purpurascens','&nbsp;(Gomont ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[549][550][551]','','',NULL,NULL,0,1,'clades:1746',0,'active','2019-07-23 12:17:09','admin'),(1748,'Leptolyngbya purpurea','(Gomont) Anagnostidis &amp; Komárek 1988&nbsp;',225,'[102]','','Species',NULL,'[552]','','',NULL,NULL,0,1,'clades:1749',0,'active','2019-07-23 13:13:13','admin'),(1749,'Lyngbya purpurea','Gomont 1892, Ann. Sci. NAt. Bot. 7, 16: 149',234,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 13:12:01','admin'),(1750,'Phormidium ramosum','Boye Petersen 1932, Bot. Icel. 2(2): 281',267,'[424]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 13:12:32','admin'),(1751,'Leptolyngbya ramosa','(Boye-Petersen) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1750',0,'active','2019-07-23 13:13:23','admin'),(1752,'Lyngbya rivulariarum','Gomont 1892, Ann. Sci. Nat. Bot. 7, 16: 148',234,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 13:12:11','admin'),(1753,'Leptolyngbya rivulariarum','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1752',0,'active','2019-07-23 13:13:29','admin'),(1754,'Phormidium rubrum','Tilden 1896, AMer. Alg. 2: 186',267,'[425]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-23 13:12:40','admin'),(1755,'Leptolyngbya rubra','(Tilden) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1754',0,'active','2019-07-23 13:13:35','admin'),(1756,'Phormidium angustissimum var. saxicola','Gardner 1932, New York Acad. Sci., Sci. Surv, Puerto Rico (2): 279',267,'[412]','','Species',NULL,'','','','Forming thin cushions on rocks in the littoral belt; Santurce, San Juan,','[26]',0,1,'',0,'active','2019-07-23 13:28:50','admin'),(1757,'Leptolyngbya saxicola','(Gardner) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1756',0,'active','2019-07-23 13:29:25','admin'),(1758,'Plectonema schmidlei','Limanowska 1912, Arch. Hydrobiol. Planktonk. 7: 364',273,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 07:36:53','admin'),(1759,'Leptolyngbya schmidlei','(Limanowska) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1758',0,'active','2019-07-25 07:38:28','admin'),(1760,'Lyngbya scottii','&nbsp;Fritsch 1912, Nat. Antarct. Exped. 1901-1904, 6: 29',234,'[384]','','Species',NULL,'','','','Granite Harbour','[2]',0,1,'',0,'active','2019-07-25 07:37:46','admin'),(1761,'Leptolyngbya scottii','(Fritsch) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'[553][554][555][556]','','',NULL,NULL,0,1,'clades:1760',0,'active','2019-07-25 07:38:38','admin'),(1762,'Phormidium scytonematicola','Gardner 1927, Mem. N.Y.Bot. Gard, 7: 42',267,'[215]','','Species',NULL,'','','','on rock by the road north of Maricao, in depressions in rock &nbsp;at Hacienda <br>Catalina','[26]',0,1,'',0,'active','2019-07-25 07:37:21','admin'),(1763,'Leptolyngbya scytonematicola','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1762',0,'active','2019-07-25 07:38:44','admin'),(1764,'Phormidium spirale','Jao 1948, Bot. Bull. Acad. Sin. 2: 169',267,'[416]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-25 07:37:28','admin'),(1765,'Leptolyngbya spiralis','&nbsp;(Jao) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1764',0,'active','2019-07-25 07:38:49','admin'),(1766,'Phormidium spirale','Jao 1948, Bot. Bull. Acad. Sin. 2: 169',1,'[416]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-07-25 07:39:43','admin'),(1767,'Phormidium subcapitatum','Petersen 1923, Arb. Bot. København 101(7): 282',267,'[427]','','Species',NULL,'','','','In soil in a potato field','[66]',0,1,'',0,'active','2019-07-25 11:53:40','admin'),(1768,'Leptolyngbya subcapitata','&nbsp;(Petersen) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1767',0,'active','2019-07-25 11:51:32','admin'),(1769,'Lyngbya subcyanea','Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 88',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-25 11:52:48','admin'),(1770,'Leptolyngbya subcyanea','(Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1769',0,'active','2019-07-25 11:51:40','admin'),(1771,'Cylindrospermopsis acuminato-crispa','Coute et Bouvy 2004. Archive für Hydrobiologie/Algological Studies 113: 69',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:48:40','admin'),(1772,'Cylindrospermopsis africana','Komárek &amp; Kling 1991. Algological Studies 61: 38',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2021-06-18 09:07:05','admin'),(1773,'Cylindrospermopsis catemaco','Komárková-Legnerová et Tavera 1996. Archiv für Hydrobiologie/Algological Studies 83: 413',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:49:20','admin'),(1774,'Cylindrospermopsis curvispora','Watanabe 1995. Bulletin of the National Museum of Nature and Science, Series B (Botany) 21 (2): 48.',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:49:49','admin'),(1775,'Raphidiopsis acuminato-crispa','(Couvy &amp; Bouvy) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1771',0,'active','2019-07-25 11:53:59','admin'),(1776,'Raphidiopsis africana','(Komárek et Kling) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1772',0,'active','2019-07-25 11:54:09','admin'),(1777,'Raphidiopsis catemaco','(Komárková-Legnerová et Tavera) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1773',0,'active','2019-07-25 11:54:28','admin'),(1778,'Raphidiopsis curvispora','(Watanabe) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1774',0,'active','2019-07-25 11:54:51','admin'),(1779,'Cylindrospermopsis cuspis','Komárek et Kling 1991. Archiv für Hydrobiologie/Algological Studies 61: 38',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:50:05','admin'),(1780,'Anabaenopsis gangetica','G.U. Nair 1967. Hydrobiologia 30(1): 147',103,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:47:45','admin'),(1781,'Lyngbya submonilifera','Frémy 1945, Bull. Mus. Nat. Hist. Nat. 17: 73',234,'[428]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-25 11:52:56','admin'),(1782,'Cylindrospermopsis helicoidea','Cronberg &amp; Komárek 2004. Nova Hedwigia 78 (1–2): 83',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:50:21','admin'),(1783,'Anabaenopsis philippinensis','W.R. Taylor 1932. American Journal of Botany 19: 462',103,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:35:50','admin'),(1784,'Cylindrospermopsis sinuosa','Coute, Leitao &amp; Sarmento 2003. Archiv für Hydrobiologie/Algological Studies &nbsp;111:',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:50:39','admin'),(1785,'Cylindropermopsis taverae','Komárek et Komárková-Legnerová 2002. Preslia 74: 229',165,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:48:05','admin'),(1786,'Leptolyngbya submonilifera','(Frémy) Senna &amp; Compère in et al. 1998, Scr. Bot. Belg. 16 : 81',225,'[429]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1781',0,'active','2019-07-25 11:51:17','admin'),(1787,'Raphidiopsis cuspis','(Komárek et Kling) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1779',0,'active','2019-07-25 11:55:05','admin'),(1788,'Raphidiopsis gangetica','(G.U. Nair) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1780',0,'active','2019-07-25 11:55:18','admin'),(1789,'Leptolyngbya subsalina','Turicchia, Ventura, Komárková &amp; Komárek 2009, Nova Hedwigia 89: 183',225,'[178]','','Species',NULL,'','BRNM 1455','3LM05S03','Dominant in mats in marshes with higher salinity; Orange Walk, Little Belize,','[95]',0,1,'',0,'active','2019-07-25 11:51:51','admin'),(1790,'Raphidiopsis helicoidea','(Cronberg et Komárek) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'','does not meet reaquirements of Art. 41.5 of ICN (basionym not clearly indicated)','Species',NULL,'','','',NULL,NULL,0,0,'clades:1782',0,'active','2019-07-25 11:55:27','admin'),(1791,'Raphidiopsis philippninensis','(W.R. Taylor) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1783',0,'active','2019-07-25 11:55:36','admin'),(1792,'Raphidiopsis raciborskii','(Woloszynska) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 144',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1793',0,'active','2019-07-25 11:55:45','admin'),(1793,'Anabaena raciborskii','Woloszynska 1912. Bulletin International de L’Academie des Sciences de Cracovie. Classe des Sciences Mathematiques et Naturelles. Série B: Sciences Naturelles: 684',102,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-25 11:47:11','admin'),(1794,'Raphidiopsis sinuosa','(Coute, Leitaio et Sarmento) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 145',290,'[426]','does not meet reaquirements of Art. 41.5 of ICN (basionym not clearly indicated)','Species',NULL,'','','',NULL,NULL,0,0,'clades:1784',0,'active','2019-07-25 11:55:54','admin'),(1795,'Phormidium subterraneum','Copeland 1936, Ann.N.Y. Acad. Sci. 36: 188',267,'[374]','','Species',NULL,'','','','freshwater, Sunken Spring, Mammoth Hot Springs','[113]',0,1,'',0,'active','2019-07-26 06:16:10','admin'),(1796,'Leptolyngbya subterranea','Umezaki &amp; M.Watanabe 1994, Jap. J. Phycol. 42: 205',225,'[231]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1795',0,'active','2019-07-26 06:16:34','admin'),(1797,'Lyngbya subtilis','West 1892, J. Royal Microscop. Soc. 1892, 6: 741',234,'[430]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-26 06:15:55','admin'),(1798,'Leptolyngbya subtilis','(West) Anagnostidis 2001, Preslia 73: 367',225,'[9]','','Species',NULL,'[558][559][560]','','',NULL,NULL,0,1,'clades:1797',0,'active','2019-07-26 06:16:40','admin'),(1799,'Lyngbya subtilissima','Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 87',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-26 11:27:38','admin'),(1800,'Leptolyngbya subtilissima','(Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'[561][562][563][564]','','',NULL,NULL,0,1,'clades:1799',0,'active','2019-07-26 11:28:33','admin'),(1801,'Phormidium subtruncatum','Voronichin 1930, Tr. Leningr. Obšč. Estestv 60(3): 69',267,'[423]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-26 11:27:17','admin'),(1802,'Leptolyngbya subtruncata','(Voronichin) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1801',0,'active','2019-07-26 11:28:40','admin'),(1803,'Phormidium subuliforme','Gomont 1892, Ann. Sci. Nat., Bot. 7, 16: 169',267,'[235]','','Species',NULL,'','','','hot stream, Sant Paul island, Pacific','',0,1,'',0,'active','2019-07-26 11:27:23','admin'),(1804,'Leptolyngbya subuliformis','(Gomont) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1803',0,'active','2019-07-26 11:28:45','admin'),(1805,'Lyngbya tenerrima','Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 106',234,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-26 12:01:52','admin'),(1806,'Leptolyngbya tenerrima','(Hansgirg) Komárek in Anagnostidis 2001, Preslia 73: 374',225,'[9]','','Species',NULL,'[565][566][567][568][569]','','',NULL,NULL,0,1,'clades:1805',0,'active','2019-07-26 12:01:17','admin'),(1807,'Leptolyngbya tentaculiformis','McGregor 2007, Freshwater Cyanoprokaryota of North-Eastern Australia 1, p. 30',225,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-26 12:52:10','admin'),(1808,'Phormidium tenue','Gomont 1892, Ann. Sci. Nat., Bot. 7, 16: 169',267,'[235]','','Species',NULL,'','','','freshwater, thermal','',0,1,'',0,'active','2019-07-26 12:51:45','admin'),(1809,'Leptolyngbya tenuis','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[570][572][575][576][577]','','',NULL,NULL,0,1,'clades:1808',0,'active','2019-07-30 07:41:26','admin'),(1810,'Plectonema terebrans','Bornet &amp; Flahault ex Gomont 1892, Ann. Sci. Nat., Bot. 7, 16: 103',273,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-29 05:56:36','admin'),(1811,'Leptolyngbya terebrans','(Bornet &amp; Flahault ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[573]','','',NULL,NULL,0,1,'clades:1810',0,'active','2019-07-29 05:57:00','admin'),(1812,'Leptolyngbya thermalis','Anagnostidis in Anagnostidis et Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[574]','','','thermal water; Nigrita','[62]',0,1,'',0,'active','2019-07-30 06:30:21','admin'),(1813,'Oscillatoria thermarum','&nbsp;Voronichin 1927, Tr. Balneol. Inst. Kavkaz. Miner. Vod. Pjatigorsk 5: 114',258,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-30 06:29:44','admin'),(1814,'Leptolyngbya thermarum','(Voronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1813',0,'active','2019-07-30 06:30:29','admin'),(1815,'Leptolyngbya thermobia','Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'[578]','','','thermal water; Kamenna Vourla','[62]',0,1,'',0,'active','2019-07-30 08:00:57','admin'),(1816,'Phormidium thermophilum','Elenkin 1914, Suesswass.-Alg. Kamtschatka Exped., organ. par Th. P. Riabouchinsky, 11: 171-172',267,'[226]','description also in Elenkin 1949','Species',NULL,'','','','thermal water; Malkinskije kliuczi, Kamchatka','[117]',0,1,'',0,'active','2019-07-30 10:37:18','admin'),(1817,'Leptolyngbya thermophila','(Elenkin) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1816',0,'active','2019-07-30 10:36:32','admin'),(1818,'Phormidium treleasii','&nbsp;Gomont 1899, Bull. Soc. Bot. France 46: &nbsp;37-38',267,'[224]','','Species',NULL,'','','','thermal water; Arkansas','[113]',0,1,'',0,'active','2019-07-30 11:01:39','admin'),(1819,'Rippkaea','Johansen et Mareš 2019. Journal of Phycology 55: 603',21,'[397]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 14:19:17','admin'),(1820,'Rippkaea orientalis','Johansen et Mareš 2019. Journal of Phycology 55: 603',1819,'[397]','','Species',NULL,'','CBFS-A017-1','PCC 8801','Soil of a rice field, tropical biome.','[44]',1,1,'',0,'active','2019-07-30 10:34:58','admin'),(1821,'Sinocapsa','Wang et Li 2019. Phytotaxa 409(3): 154',23,'[431]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:45:40','admin'),(1822,'Sinocapsa zengkensis','Wang et Li 2019. Phytotaxa 409(3): 154',1821,'[431]','','Species',NULL,'','HBI CHAB6571','CHAB 6571','crust samples on an exposed depression of rough concrete surface from a rural house roof','[38]',1,1,'',0,'active','2019-07-30 10:35:55','admin'),(1823,'Leptolyngbya treleasii','(Gomont) Anagnostidis &amp; Komárek 1988, &nbsp;Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[579]','','',NULL,NULL,0,1,'clades:1818',0,'active','2019-07-31 06:02:34','admin'),(1824,'Phormidium truncatum','Lemmermann 1908, <em>A</em>rch. Hydrobiol. Planktonk. 4: 189',267,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-31 06:01:22','admin'),(1825,'Leptolyngbya truncata','(Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1824',0,'active','2019-07-31 06:02:38','admin'),(1826,'Phormidium valderianum','Gomont 1892, Ann. Sci. Nat. Bot. 7, 16: 167',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-31 06:01:04','admin'),(1827,'Leptolyngbya valderiana','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[580][581][582][583][584][585][586][587][588][589]','','',NULL,NULL,0,1,'clades:1826',0,'active','2019-07-31 06:02:43','admin'),(1828,'Lyngbya vandenberghenii','Symoenes in Symoenes et van den Werff 1951, Bull. Soc. Roy. Bot. Belg. 83: 214',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-07-31 06:01:40','admin'),(1829,'Leptolyngbya vandenberghenii','(Symoens) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1828',0,'active','2019-07-31 06:02:46','admin'),(1830,'Phormidium vesiculosum','Copeland 1936, Ann. N.Y. Acad. Sci. 36: 172',267,'[374]','','Species',NULL,'','','','thermal eater, Yellowstone National Park','[113]',0,1,'',0,'active','2019-07-31 06:01:10','admin'),(1831,'Leptolyngbya vesiculosa','(Copeland) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1830',0,'active','2019-07-31 06:02:50','admin'),(1832,'Leptolyngbya voronichiniana','Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','nomen novum; diagnosis <em>Ph. tenuissimum</em> Voronichin 1930','Species',NULL,'[590][591][595]','','',NULL,NULL,0,1,'',0,'active','2019-07-31 12:17:01','admin'),(1833,'Phormidium laminosum f. weedii','Tilden 1898, Bot. Gaz. 25: 99-100',267,'[433]','','Species',NULL,'','','','thermal water; overflow of channel (temperature 49-54.5<sup>o</sup>C), Spasmodic Geyser, Yellowstone National Park','[113]',0,1,'',0,'active','2019-07-31 11:00:38','admin'),(1834,'Leptolyngbya weedii','(Tilden) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'[592]','','',NULL,NULL,0,1,'clades:1833',0,'active','2019-07-31 11:01:42','admin'),(1835,'Phormidium weissii','Drouet 1939, Field Mus. Nat. His., Bot. ser, 20(1): 10',267,'[434]','','Species',NULL,'','','','brackish and marine water,','[113]',0,1,'',0,'active','2019-07-31 11:00:17','admin'),(1836,'Leptolyngbya weissii','(Drouet) Anagnostidis 2001, Preslia 73: 368',225,'[9]','','Species',NULL,'[593]','','',NULL,NULL,0,1,'clades:1835',0,'active','2019-07-31 11:01:21','admin'),(1837,'Plectonema yellowstonense','Prát 1929, Stud<em>y </em>on biolithog., p. 98',273,'[435]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-31 10:59:53','admin'),(1838,'Leptolyngbya yellowstonensis','(Prát) Anagnostidis &amp; Komárek 1988, Algolog. STud. 50-53: 393',225,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1837',0,'active','2019-07-31 11:01:05','admin'),(1839,'Phormidium woronichinii','Anissimova in Elenkin 1949, Monogr. Algarum, p. 1467',267,'[226]','','Species',NULL,'','','','brackish; Slaviansk','[118]',0,1,'',0,'active','2019-07-31 11:00:12','admin'),(1840,'Leptolyngbya woronichinii','(Anissimova) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 393',225,'[102]','','Species',NULL,'[594]','','',NULL,NULL,0,1,'clades:1839',0,'active','2019-07-31 11:01:12','admin'),(1841,'Leptolyngbya undosa','(Čado) Anagnostidis &amp; Komárek 1988',225,'','without combination, description in Komárek &amp; Anagnostidis 2005,&nbsp;','Species',NULL,'','','',NULL,NULL,0,0,'clades:1842',0,'active','2019-07-31 12:40:15','admin'),(1842,'Phormidium undosum','Čado 1958, Zbor. rab. filos. fak Skopje 5(21): 8',267,'[382]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-07-31 12:39:49','admin'),(1843,'Arthrospira argentina','(Frenguelli) Guarrera &amp; Kühnemann 1949, Lilloa 19: 297',108,'[437]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1844',0,'active','2019-08-05 05:37:16','admin'),(1844,'Spirulina argentina','&nbsp;Frenguelli 1937, Notas Mus. la Plata 2, Bot. 15: 165',316,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-08-05 05:50:17','admin'),(1845,'Spirulina amethystina','Buell 1938, Bull. Torrey Bot. Club 65: 389',316,'[94]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-05 05:49:54','admin'),(1846,'Arthrospira amethystina','(Buell) De Toni 1949, Gen. &amp; Sp. Myx. 1: 75',108,'','','Species',NULL,'','','','Benthic, in heliothermal waters; Lake of the Isles Lagoon, Minnessota','[113]',0,1,'clades:1845',0,'active','2020-02-27 12:09:42','admin'),(1847,'Spirulina ardissonei','Cohn ex Rabenhorst 1865, Flora Europ. Algarum, p. 91',316,'[438]','','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2019-08-05 05:50:06','admin'),(1848,'Arthrospira ardissonei','(Cohn) Forti 1907, Syloge Algarum, p. 206',108,'[436]','','Species',NULL,'','','','marine; near Genoa','[69]',0,1,'clades:1847',0,'active','2019-08-05 05:36:32','admin'),(1849,'Oscillatoria balkrishnanii','(Kamat) Rino 1972, Rev. Cienc. Biol. Ser. A 5: 137',258,'[495]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-02-27 14:00:02','admin'),(1850,'Arthrospira balkrishnanii','Kamat 1963, Hydrobiologia 22(3-4): 278',108,'[439]','','Species',NULL,'','','','puddles; in Kolhapur','[156]',0,1,'clades:1849',0,'active','2020-02-27 13:46:46','admin'),(1851,'Arthrospira baryana','Stizenberger 1854',108,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,0,NULL,0,'active','2019-08-05 05:49:03','admin'),(1852,'Arthrospira braunii','&nbsp;(Kützing) Forti 1907, Sylloge Algarum, &nbsp;Vol. V, p. 206',108,'[436]','','Species',NULL,'','','','Berlin','[60]',0,1,'clades:1853',0,'active','2020-03-02 12:28:34','admin'),(1853,'Spirulina braunii','Kützing 1863, Rab. Fl. Eur. Alg. II, p. 91',316,'','','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-03-02 12:26:54','admin'),(1854,'Arthrospira brevis','Wang 1933',108,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-07 12:26:07','admin'),(1855,'Pseudoscytonema capitatum','(Jaag) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 432',286,'[102]','','Species',NULL,'[597]','','',NULL,NULL,0,1,'clades:1856',0,'active','2019-08-08 07:32:54','admin'),(1856,'Plectonema capitata','Jaag 1935, Ber. schweiz. bot. Gess. 44: 442',273,'[440]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-08 11:57:12','admin'),(1857,'Plectonema congregationis','Schwabe 1962, Rev. Algol. 2: 90',273,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-08-08 11:57:18','admin'),(1858,'Pseudoscytonema congregationis','(Schwabe) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 432',286,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1857',0,'active','2019-08-08 11:58:08','admin'),(1859,'Plectonema endolithicum','Ercegovic 1932, Rad Jugosl. Akad. Znan. Umjet. Zagreb 244: 159',273,'[441]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-08 11:57:33','admin'),(1860,'Pseudoscytonema endolithicum','(Ercegovic) &nbsp;Komárek &amp; Anagnostidis 2005, Suesswasser. Mitt. Europe, vol.19/2: 546',286,'[31]','citation in book P. endolithicum Anagnostidis 2001, but there in this paper is not combination','Species',NULL,'[492]','','',NULL,NULL,0,1,'clades:1859',0,'active','2019-08-08 11:58:12','admin'),(1861,'Plectonema malayense','&nbsp;Biswas 1929, J. Fed. Malay State Mus. 14: 411',273,'[442]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-08 11:57:44','admin'),(1862,'Lyngbya sphaerocephala','Jao et Lee in Jao et al. 1974, Rep. Sci. Res. Exped. Qomolangma Feng Reg., p. 124',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-08-08 11:56:51','admin'),(1863,'Pseudoscytonema sphaerocephalum','&nbsp;(Jao et Lee) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 434',286,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1862',0,'active','2019-08-08 11:58:29','admin'),(1864,'Plectonema spongiosum','Schwabe 1962, Nova Hedwigia 4(3-4): 523',273,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-08-08 11:57:52','admin'),(1865,'Pseudoscytonema spongiosum','(Schwabe) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 434',286,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1864',0,'active','2019-08-08 11:58:37','admin'),(1866,'Lyngbya subclavata','Starmach 1958, Fragm. Flor. Geobot. Polonica 3(2): 147',234,'[443]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-08 11:56:57','admin'),(1867,'Pseudoscytonema subclavatum','(Starmach) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 434',286,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1866',0,'active','2019-08-08 11:58:44','admin'),(1868,'Sirocoleum kurzii','Gomont 1892, Ann. Sci. Nat., Bot.7, 15: 349',308,'[145]','','Species',NULL,'[598]','','',NULL,NULL,0,1,'',0,'active','2019-08-28 12:25:58','admin'),(1869,'Sirocoleum indicum','Zeller 1873, &nbsp;J. Asiatic Soc. Bengal 42(2): 178',308,'[444]','','Species',NULL,'','','','wetted maritim rocks; Arracan, Akyab,','[161]',0,1,'',1,'active','2019-08-29 11:54:47','admin'),(1870,'Sirocoleum cyaneum','Crouan in Schram et Mazé 1865, Essai &nbsp;de la Guadeloupe, p. 30',308,'[445]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-29 13:14:49','admin'),(1871,'Sirocoleum lyngbiiforme','Crouan in Schram et Mazé 1865, Essai de la Guadeloupe, p. 30',308,'[445]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-29 13:15:21','admin'),(1872,'Sirocoleum indicum','Zeller 1873, J. Asiatic Soc. Bengal 42(2): 178-179',308,'[444]','','Species',NULL,'','','','wetted maritime rocks; Arracan, Akyab','[161]',0,1,'',0,'active','2019-08-29 13:14:55','admin'),(1873,'Gardnerula jensenii','(Weber van Bosse) Tseng &amp; Hua 1982, Chin. J. Oceanol. Limnol. 1(1): 116',183,'[446]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1874',0,'active','2019-08-29 13:15:46','admin'),(1874,'Sirocoleum jensenii','Weber Bosse 1926, Vidensk. Medd. Dansk Naturhist. For. 81: 68',308,'[447]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-08-29 13:15:14','admin'),(1875,'Koinonema','Buch, Martins et Branco 2017, J. Phycol. 53: 1102-1103',50,'[448]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-09-02 12:34:21','admin'),(1876,'Koinonema pervagatum','Buch, Martins et Branco 2017, J. Phycol. 53: 1103',1875,'[448]','','Species',NULL,'','SJRP 32540','63PC','pond bottom; Sao Jose do Rio Preto Municipal Reservoir Park, municipality of Sao Jose do Rio Preto, Sao Paulo State','[172]',1,1,'',0,'active','2019-09-02 12:34:37','admin'),(1877,'Hassallia littoralis','González-Resendiz et León-Tejera 2013. Phytotaxa 137(1): 37',200,'[449]','','Species',NULL,'','FCME PTM9586','','igneous rocks near seaside, slightly wetted by the sea breeze and totally exposed to sunlight','[100]',0,1,'',0,'active','2019-10-04 05:12:49','admin'),(1878,'Symphyonema cavernicola','Asencio, Aboal et L. Hoffmann 1996. Arch. Hydrobiol./Algological Studies 83: 75',322,'[451]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-10-14 13:10:01','admin'),(1879,'Lyngbya aureo-fulva','West W. et G.S., 1897, J. Bot. 35: 298',234,'[370]','','Species',NULL,'','','','Pungo Andongo','[185]',0,1,'',0,'active','2019-10-14 11:42:42','admin'),(1880,'Porphyrosiphon aureo-fulvus','(West &amp; West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1879',0,'active','2019-10-14 11:41:42','admin'),(1881,'Lyngbya calcifera','Brühl &amp; Biswas 1924, J. Dept. Sci. Univ. Calcutta 5 (Bot.): 12',234,'[453]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-10-15 12:19:59','admin'),(1882,'Porphyrosiphon calciferus','&nbsp;(Brühl &amp; Biswas) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1881',0,'active','2019-10-15 12:20:42','admin'),(1883,'Myxacorys almedinensis','Soares, Tiago et Portugal 2019. Phytotaxa 419(1): 80',1650,'[454]','','Species',NULL,'','COI 00094076','ULC 467 = DSM 109598','surface of limestone walls','[82]',0,1,'',0,'active','2019-10-15 12:19:18','admin'),(1884,'Porphyrosiphon ceylanicus','(Wille) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'[601][602][603]','','',NULL,NULL,0,1,'clades:1885',0,'active','2019-10-18 13:14:35','admin'),(1885,'Lyngbya ceylanica','Wille in Rechinger 1914, Denskrch. mathem.-natur. 91: 161',234,'[455]','Nr 260G, 2714, 2740','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>forest undergrowth</span></span>','[165]',0,1,'',0,'active','2019-10-18 13:14:04','admin'),(1886,'Porphyrosiphon corbierei','(Frémy) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'[605]','','',NULL,NULL,0,1,'clades:1887',0,'active','2019-10-18 13:14:43','admin'),(1887,'Lyngbya corbierei','Frémy 1923, Bull. Soc. Linn. Normandie 7(6): 15',234,'[456]','','Species',NULL,'','','','Carentan','[59]',0,1,'',0,'active','2019-10-18 13:14:11','admin'),(1888,'Porphyrosiphon dendrobius','(Brühl &amp; Biswas) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'[606][607]','','',NULL,NULL,0,1,'clades:1889',0,'active','2019-10-18 13:16:36','admin'),(1889,'Lyngbya dendrobia','Brühl &amp; Biswas 1923, J. Dept. Sci. Calcutta Univ. 5: 8',234,'[453]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-10-18 13:14:19','admin'),(1890,'Porphyrosiphon fuscus','Gomont ex Frémy 1927, Bull. Mus. Nat. Hist. Natur. 33: 115',277,'[Fré]','Ex Coll. &nbsp;Henry , no. 358 et 363','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-11-04 13:26:49','admin'),(1891,'Euryhalinema','Chakraborty et Mukherjee 2019. Phytotaxa 422(1): 70',416,'[457]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 11:59:51','admin'),(1892,'Euryhalinema mangrovii','Chakraborty et Mukherjee 2019. Phytotaxa 422(1): 70',1891,'[457]','','Species',NULL,'','MCC 3171 (cryopreserved)','AP9F','on soil','[156]',1,1,'',0,'active','2019-10-30 05:40:47','admin'),(1893,'Leptoelongatus','Chakraborty et Mukherjee 2019. Phytotaxa 422(1): 70',2544,'[457]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:34:04','admin'),(1894,'Leptoelongatus litoralis','Chakraborty et Mukherjee 2019. Phytotaxa 422(1): 70',1893,'[457]','','Species',NULL,'','MCC 3170 (cryopreserved)','AP25','soil surface','[156]',1,1,'',0,'active','2019-10-30 05:49:49','admin'),(1895,'Porphyrosiphon fuscus','Gomont ex Frémy 1927',277,'[458]','Ex Coll. Henry, no &nbsp;358 et 363.&nbsp;','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>Cochinchinam, near Saigon</span></span>','[168]',0,1,'',0,'active','2019-11-05 13:07:07','admin'),(1896,'Porphyrosiphon kaernbachii','(Hennings) De Toni 1892',277,'','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1898',0,'active','2019-11-06 06:37:00','admin'),(1897,'Porphyrosiphon kashyapii','(Ghose) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1899',0,'active','2019-11-06 06:37:20','admin'),(1898,'Scytonema kaernbachii','Hennings 1892',302,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-06 06:36:30','admin'),(1899,'Lyngbya kashyapii','Ghose 1924, J. Linn. Soc. (Botany) 46: 339',234,'[459]','','Species',NULL,'','','','on moist ground which has been under water for sometime, &nbsp;drying tanks of the Shalamar Gardens, Lahore','[253]',0,1,'',0,'active','2019-11-06 06:37:45','admin'),(1900,'Stigonema jureiensis','Hentsche et Sant Anna 2019. Fottea 19(2): 187',321,'[460]','','Species',NULL,'','SP 427311','','On a humid igneous rock in a dense rainforest area.','[172]',0,1,'',0,'active','2019-11-06 06:35:51','admin'),(1901,'Nodosilinea signiensis','Radzi et Merican 2020. Notulae Algarum 125',565,'[461][543]','','Species',NULL,'','USM 11833','','Mats in cracks and crevices in rocks and beneath loose fragments of stone collected from west-facing slope below Robin Peak','[2]',0,1,'',0,'active','2020-05-14 12:30:03','admin'),(1902,'Porphyrosiphon latissimum','Kaštovský, Fučíková et Bohunická &nbsp;in Kaštovský et al. 2016, Phytotaxa 247(3): 160',277,'[462]','','Species',NULL,'','CBFS! A-020,','','sandstone rocks, on top of Churí-tepui and Roraima','[183]',0,1,'',0,'active','2019-11-07 14:21:16','admin'),(1903,'Porphyrosiphon lomniczensis','(Kol) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1904',0,'active','2019-11-08 09:00:33','admin'),(1904,'Lyngbya lomniczensis','Kol 1926, Folia crypt. (Szeged) 1(4): 224',234,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-11 12:18:51','admin'),(1905,'Porphyrosiphon luteus','(Gomont ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'[609]','','',NULL,NULL,0,1,'clades:1906',0,'active','2019-11-11 12:18:34','admin'),(1906,'Lyngbya lutea','Gomont ex Gomont 1892, Ann. Sci. Nat., Bot., Série 7, 16: 141',234,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-11 12:18:55','admin'),(1907,'Lyngbya martensiana','Meneghini ex Gomont 1892',234,'[235]','','Species',NULL,'[617]','','','thermal','[69]',0,1,'',0,'active','2019-11-11 13:28:37','admin'),(1908,'Arthrospira miniata','Gomont 1892, Ann. Sci. Nat., Bot., Série 7 16: 248',108,'[235]','','Species',NULL,'[618][619][620][794]','','',NULL,NULL,0,1,'',0,'active','2020-03-17 13:57:14','admin'),(1909,'Porphyrosiphon robustus','Gardner 1927, Mem. New York Bot. Gard. 7: 41-42',277,'[215]','types no. 1570, 1185 a','Species',NULL,'','','','Growing on rock among moss, Utuado; &nbsp;on red soil, <em>Mayagüez</em>','[26]',0,1,'',0,'active','2019-11-11 14:31:35','admin'),(1910,'Porphyrosiphon samoensis','(Wille) Drouet 1937, Am. J. Bot. 24(9): 602',277,'[463]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-12 12:59:38','admin'),(1911,'Porphyrosiphon kaernbachii var. samoensis','&nbsp;Wille 1914, Bot. Zoolog. Ergebnise, Teil VI: 145',277,'[455]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1910',0,'active','2019-11-12 12:59:34','admin'),(1912,'Porphyrosiphon shackletonii','(West &amp; G.S.West) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1913',0,'active','2019-11-12 13:00:22','admin'),(1913,'Lyngbya shackletonii','West &amp; G.S.West 1911, Brit. Antarc. Exped., part VII, vol 1. : 289',234,'[282]','','Species',NULL,'','','','freshwater; Lake at Hut Point','[2]',0,1,'',0,'active','2019-11-12 12:59:01','admin'),(1914,'Phormidium stagninum','Anagnostidis 2001, Preslia 73: 371',267,'[9]','Basionym &nbsp;= Lyngbya stagnina Kützing sensu auctorum (Skuja 1929, Kiss 1968)','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2019-11-12 14:27:49','admin'),(1915,'Porphyrosiphon stagninum','(Kützing ) Anagnostidis 2001, Preslia 73: 371',277,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1916',0,'active','2019-11-12 14:28:05','admin'),(1916,'Lyngbya stagnina','&nbsp;Kützing 1843, Phycologia generalis, p. &nbsp;22',234,'[135]','pre-starting points name','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2019-11-12 14:27:34','admin'),(1917,'Porphyrosiphon velasquezii','Drouet 1942, Publ. Field Mus. Nat. Hist. Bot. Ser. 20(6): 130',277,'[465]','','Species',NULL,'','','','Forming crusts on soil wet intermittently with fresh water','[163]',0,1,'',0,'active','2019-11-12 14:28:08','admin'),(1918,'Porphyrosiphon versicolor','&nbsp;(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 409',277,'','','Species',NULL,'[623][624][625][626]','','',NULL,NULL,0,1,'clades:1919',0,'active','2019-11-14 12:07:12','admin'),(1919,'Lyngbya versicolor','Gomont 1892, Ann. Sci. Nat., Bot., Série 7, 16: 147',234,'[235]','','Species',NULL,'','','','freshwater, puddles, pools','[59]',0,1,'',0,'active','2019-11-14 11:46:43','admin'),(1920,'Phormidium granulatum','(Gardner) Anagnostidis 2001, Preslia 73: 371',267,'[9]','','Species',NULL,'[631]','','',NULL,NULL,0,1,'clades:827',0,'active','2019-11-14 14:04:45','admin'),(1921,'Phormidium griseo-violaceum','(Skuja) Anagnostidis 2001, Preslia 73: 370',267,'[9]','','Species',NULL,'[632]','','',NULL,NULL,0,1,'clades:828',0,'active','2019-11-15 12:03:56','admin'),(1922,'Phormidium ingricum','(Woronichin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413',267,'[102]','','Species',NULL,'[633]','','',NULL,NULL,0,1,'clades:829',0,'active','2019-11-15 12:03:49','admin'),(1923,'Oscillatoria ingrica','Woronichin 1931, Acta Horti Bot. Acad. Sci. URSS 44: 225',1,'','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-11-14 14:26:12','admin'),(1924,'Tychonema rhodonema','&nbsp;(Skuja) Anagnostidis et Komárek 1988, Algolog. Stud. 50-53: 413',1,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-11-15 12:07:49','admin'),(1925,'Blennothrix boergesenii','(Gardner) Anagnostidis 2001, Preslia 73: 373',113,'[9]','','Species',NULL,'[656]','','',NULL,NULL,0,1,'clades:1926',0,'active','2019-11-19 13:07:27','admin'),(1926,'Hydrocoleum boergesenii','Gardner 1932, Sci. Surv. Porto Rico, Vol. 8(2): &nbsp;289',211,'[412]','','Species',NULL,'','','','spring; Christianssted\'s Lagoon, St. Croix','[35]',0,1,'',0,'active','2019-11-19 13:07:50','admin'),(1927,'Blennothrix brebissonii','(Kützing ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 429',113,'[102]','','Species',NULL,'[657][658][660]','','',NULL,NULL,0,1,'clades:1928',0,'active','2020-04-16 11:28:35','admin'),(1928,'Hydrocoleum brebissonii','&nbsp;Kützing ex Gomont 1892, Ann. Sci. Nat. Bot., Ser. 7, 15: 343',211,'[145]','','Species',NULL,'','','','freshwater; Falaise','[59]',0,1,'',0,'active','2019-11-20 11:31:06','admin'),(1929,'Blennothrix bremii','(Nägeli ) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53:429',113,'[102]','','Species',NULL,'[661][662]','','',NULL,NULL,0,1,'clades:1930',0,'active','2019-11-20 11:30:51','admin'),(1930,'Hydrocoleum bremii','Nägeli &nbsp;in Kützing 1849, Spec. Algarum, p. 892',211,'[466]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-20 11:31:12','admin'),(1931,'Hydrocoleum caespitulum','(Harvey) Chapman 1961',211,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-11-21 12:21:17','admin'),(1932,'Hydrocoleum cantharidosmum','Gomont 1892, Ann. Sci. Nat., Bot., Série 7 15: 336',211,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-11-21 12:21:23','admin'),(1933,'Hydrocoleum caput-avis','Fiorini-Mazzanti ex Forti 1907',211,'[436]','','Species',NULL,'','','','thermal spring, near Terracina','[69]',0,1,'',0,'active','2019-11-21 14:13:57','admin'),(1934,'Hydrocoleum cavanillesii','González Guerrero 1946',211,'[467]','','Species',NULL,'','','','marine, near Puerto Real (Cádiz)','[88]',0,1,'',0,'active','2019-11-21 14:14:05','admin'),(1935,'Hydrocoleum coccineum','Gomont 1892, Ann. Sci. Nat. Bot., ser. 7, 15: 342',211,'[145]','','Species',NULL,'','','','marine; near Antibes','[59]',0,1,'',0,'active','2019-11-21 14:14:17','admin'),(1936,'Symplocastrum coccineum','(Gomont) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1935',0,'active','2019-11-21 14:13:34','admin'),(1937,'Hydrocoleum codicola','Setchell &amp; Gardner 1924, Proc. Calif. Acad. Sci, 4th Ser. 12: 702',211,'[468]','Type: No. 1319, Herb. Calif. Acad. Sci., collected by Ivan M. Johnston (No. 8a), in June, at San Marcos Island, Gulf of California.','Species',NULL,'','','','marine; Gulf of California, San MArcos Island','[113]',0,1,'',0,'active','2019-11-22 12:46:06','admin'),(1938,'Blennothrix coerulea','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 429',113,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1939',0,'active','2019-11-25 13:49:58','admin'),(1939,'Hydrocoleum coeruleum','Gardner 1927, Univ. Calif. Publ. Bot. 14(1): 3',211,'[469]','Type A289, in the Farlow Herbarium, Harvard University, Cambridge, Mass','Species',NULL,'','','','In mountain streams. Kuliang, near Foochow','[38]',0,1,'',0,'active','2019-11-25 13:51:05','admin'),(1940,'Blennothrix comoides','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 429',113,'[102]','','Species',NULL,'[663]','','',NULL,NULL,0,1,'clades:1941',0,'active','2019-11-25 14:07:40','admin'),(1941,'Hydrocoleum comoides','Gomont 1892, Ann. Sci. Nat Bot. Ser. 7, 15: 335',211,'[145]','','Species',NULL,'','','','marine','[13]',0,1,'',0,'active','2019-11-27 09:34:08','admin'),(1942,'Blennothrix confluens','&nbsp;(Setchell &amp; Gardner) Umezaki 1995, J. Jap. Bot. 70(3): 136',113,'[470]','','Species',NULL,'[664]','','',NULL,NULL,0,1,'clades:1943',0,'active','2019-11-27 09:33:07','admin'),(1943,'Microcoleus confluens','Setchell &amp; N.L.Gardner &nbsp;in Gardner 1918, Univ. Cal. Publ. Bot. 6: 471',245,'[406]','Type no. 1641, Gardner','Species',NULL,'','','','on rocks in the upper part of the littoral belt, San Francisco, California','[113]',0,1,'',0,'active','2019-11-27 09:33:33','admin'),(1944,'Scytonema pachmarhiense','Saraf et Singh 2018. FEMS Microbiology Letters 365(15): 7',302,'[471]','','Species',NULL,'','MCC 3343 (cryopreserved)','MCC 3343','freshwater body','[156]',0,1,'',0,'active','2019-11-27 09:32:43','admin'),(1945,'Hydrocoleum eatonii','Reinsch ex Geitler 1932, Kryptogamen Flora p. 1152',211,'[305]','','Species',NULL,'','','','freshwater, <span lang=\'en\'><span title=\'\'>on water mosses</span></span>, Kerguelen Islands','',0,1,'',0,'active','2019-12-03 08:00:43','admin'),(1946,'Hydrocoleum floccosum','Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 15: 341',211,'[145]','','Species',NULL,'[668][669]','','','marine, Mediterranean Sea, Sainte-Marguerite Island','[59]',0,1,'',0,'active','2019-12-03 08:01:39','admin'),(1947,'Hydrocoleum fontanum','Jao 1944, Sinensia 15: 89',211,'[450]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-03 08:00:49','admin'),(1948,'Blennothrix fontana','(Jao) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 429',113,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1947',0,'active','2019-12-03 09:10:57','admin'),(1949,'Hydrocoleum glutinosum','Gomont ex Gomont 1892, Ann. Sci. NAt. Bot. ser. 7, 15: 339',211,'[145]','','Species',NULL,'','','','marine,','',0,1,'',0,'active','2019-12-03 08:02:03','admin'),(1950,'Blennothrix glutinosa','(Gomont ex Gomont) Anagnostidis &amp; Komárek in Anagnostidis 2001, Preslia 73: 373',113,'[9]','','Species',NULL,'[672][673]','','',NULL,NULL,0,1,'clades:1949',0,'active','2020-04-07 07:38:34','admin'),(1951,'Blennothrix groesbeckiana','(Drouet) Anagnostidis 2001, Preslia 73: 373',113,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1953',0,'active','2019-12-03 12:57:24','admin'),(1952,'Hydrocoleum groesbeckianum','Drouet 1942, Publ. Field Mus. Nat. Hist., Bot. Ser. 20(6): 137',1,'[465]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-12-02 14:30:13','admin'),(1953,'Hydrocoleum groesbeckianum','Drouet 1943, Bot. Ser. Field Mus. Nat. Hist., &nbsp;20(7): 166',211,'[473]','TYPE in Cryptogamic Herbarium of Field Museum, Groesbeck 271, 272, Nov. 1940','Species',NULL,'','','','in the travertine quarry near Bridgeport, California','[113]',0,1,'',0,'active','2019-12-04 07:31:01','admin'),(1954,'Hydrocoleum heterotrichum','Gomont ex Gomont 1892, Ann. Sci. Nat., Bot. Ser. 7, 15: 342',211,'[145]','','Species',NULL,'','','','freshwater, <span lang=\'en\'><span title=\'\'>at the source of the river</span></span>, Dalmatia','[53]',0,1,'',0,'active','2019-12-04 07:31:04','admin'),(1955,'Blennothrix heterotricha','(Gomont ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 429',113,'[102]','','Species',NULL,'[1007][1008][1009][1010][1011][1012]','','',NULL,NULL,0,1,'clades:1954',0,'active','2020-04-16 11:25:17','admin'),(1956,'Hydrocoleum hieronymii','Richter in Hauck &amp; Richter 1892, <em>Phykotheka universalis</em> no.543',211,'[474]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-05 08:26:27','admin'),(1957,'Hydrocoleum kurzii','Martens 1869, Flora Allgem.e Bot. Zeit. 52: 235',211,'[475]','pre-starting point name; no 1686 in Calcutta','Species',NULL,'','','','','[156]',0,0,'',0,'active','2019-12-05 08:26:17','admin'),(1958,'Hydrocoleum lauterbachii','Hieronymus et Schmidle in Lauterbach &amp; Schumann 1901, Pfl. Deutsch. Schutzg. Südsee, p. 3',211,'','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>Freshwater, in slowly flowing water in Kaiser-Wilhelms-Land</span></span>','[139]',0,1,'',0,'active','2019-12-05 08:26:11','admin'),(1959,'Blennothrix lauterbachii','(Hieronymus &amp; Schmidle) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 430',113,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1958',0,'active','2019-12-05 08:26:42','admin'),(1960,'Dulcicalothrix','Saraf, Sudkar, Dawda, Gaysina, Gabidullin, Kumat, Behere, Kotulkar, Batule et Singh 2019. FEMS Microbiology Letters 366: fnz219: 8',1961,'[476]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-12-05 09:09:35','admin'),(1961,'Calotrichaceae','Bennet et Murray 1889',9,'[476]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2019-12-05 09:20:32','admin'),(1962,'Dulcicalothrix necridiiformis','Saraf, Sudkar, Dawda, Gaysina, Gabidullin, Kumat, Behere, Kotulkar, &nbsp;Batule et Singh 2019. FEMS Microbiology Letters 366: fnz219: 8',1960,'[476]','','Species',NULL,'','MCC 3314 (metabolically inactive)','MCC 3314','oligotrophicwater body as bluish green macroscopic colonies found submerged in shallow water. The water temperature at the time of collection was 38.2◦C while the pH was recorded as 7.3','[156]',1,1,'',0,'active','2021-06-18 08:53:21','admin'),(1963,'Calothrix desertica','Schwabe 1960. Österreichische Botanische Zeitschrift 107: 282',119,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-12-05 09:19:47','admin'),(1964,'Dulcicalothrix desertica','(Schwabe) Saraf, Sudkar, Dawda, Gaysina, Gabidullin, Kumat, Behere, Kotulkar, Batule et Singh 2019. FEMS Microbiology Letters 366: fnz219: 9',1960,'[476]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1963',0,'active','2019-12-05 09:20:02','admin'),(1965,'Hydrocoleum lenormandii','Martens 1871, Proc. Asiat. Soc. Bengal 1871: 173',211,'[477]','pre-starting point name','Species',NULL,'','','','salt lake near Calcutta on tsubmerged grasses','[156]',0,0,'',0,'active','2019-12-06 08:14:33','admin'),(1966,'Hydrocoleum lyngbyaceum','Kützing ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. <em>7,</em> 15: 337',211,'[145]','','Species',NULL,'','','','marine, north coast of Galia','[59]',0,1,'',0,'active','2019-12-06 08:14:43','admin'),(1967,'Blennothrix lyngbyacea','(Kützing ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 430',113,'[102]','','Species',NULL,'[681][682][683][684][685][686][687][688][689][975][976][977]','','',NULL,NULL,0,1,'clades:1966',0,'active','2020-04-03 12:17:01','admin'),(1968,'Hydrocoleum violaceum','Martens ex Geitler 1932, Kryptogamen Flora p. 1152',211,'[305]','','Species',NULL,'[690]','','','freshwater, in stagnant water, Calcutta','[156]',0,1,'',0,'active','2019-12-06 08:14:54','admin'),(1969,'Neowollea','Tawong 2019',34,'[478][608]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-22 13:19:57','admin'),(1970,'Neowollea manoromense','Tawong 2019. Phytotaxa 424(1): 3',1969,'[478][608]','','Species',NULL,'','QBG 132168','NUACC15','shallow freshwater pond','[166]',1,1,'',0,'active','2022-03-22 13:20:39','admin'),(1971,'Hydrocoleum majus','Holden 1899, Rhodora 1: 197',211,'[479]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-09 07:47:19','admin'),(1972,'Blennothrix majus','(Holden) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 430',113,'[102]','','Species',NULL,'[691]','','',NULL,NULL,0,1,'clades:1971',0,'active','2019-12-09 07:48:51','admin'),(1973,'Hydrocoleum meneghinianum','Kützing ex Forti 1907, Sylloge algarum, p. 325',211,'[436]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-11 12:14:10','admin'),(1974,'Hydrocoleum mirificum','Jao 1948, Bot. Bull. Acad. Sinica 2: 172',211,'[416]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-11 12:14:39','admin'),(1975,'Blennothrix mirifica','&nbsp;(Jao) Anagnostidis 2001, Preslia 73: 373',113,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1974',0,'active','2019-12-11 12:14:57','admin'),(1976,'Hydrocoleum muscicola','Hansgirg ex Forti 1907, Sylloge algarum, p. 323',211,'[436]','','Species',NULL,'','','','freshwater; river Ombla, Dalmatia','[53]',0,1,'',0,'active','2019-12-11 12:14:30','admin'),(1977,'Hydrocoleum oligotrichum','Braun ex Gomont 1892, Ann. Sci. Nat. Bot., Ser. 7, 15: 345',211,'[145]','','Species',NULL,'[692]','','','calcareous rocks, near Basel','[91]',0,1,'',0,'active','2019-12-11 12:14:17','admin'),(1978,'Symplocastrum oligotrichum','(Braun ex Gomont) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1977',0,'active','2019-12-11 12:15:27','admin'),(1979,'Hydrocoleum penicillatum','Taylor 1929, Bull. Torrey Bot. Club 56: 201',211,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2019-12-12 07:59:34','admin'),(1980,'Hydrocoleum platense','Nordstedt in Wittrock &amp; Nordstedt 1889, Botan, Notiser 1889(4): 168',211,'[480]','','Species',NULL,'','','','freshwater, <span lang=\'en\'><span title=\'\'>the</span><span title=\'\'>stones</span><span title=\'\'>on the</span><span title=\'\'>banks of</span><span title=\'\'>the Rio de la</span><span title=\'\'>Plata (</span><span title=\'\'>near </span><span title=\'\'>Montevideo','[182]',0,1,'',0,'active','2019-12-12 07:59:38','admin'),(1981,'Hydrocoleum ravenelii','Wolle ex Forti 1907, Sylloge Algarum, p. 322',211,'[436]','','Species',NULL,'[693]','','','freshwater, Texas','[113]',0,1,'',0,'active','2019-12-12 07:59:49','admin'),(1982,'Blennothrix ravenelii','(Wolle ex Forti) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 430',113,'[102]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1981',0,'active','2019-12-12 07:59:16','admin'),(1983,'Hydrocoleum rivularioides','Hansgirg 1892, <em>Sitzungsberi. Königl. Böh. Gesell. Wiss. Mat.-nat. Classe</em> 1892: 141',211,'[481]','','Species',NULL,'','','','freshwater, <span lang=\'en\'><span title=\'\'>grows on rocks</span></span> near Kardaun, South Tirolia','[49]',0,1,'',0,'active','2019-12-13 12:21:48','admin'),(1984,'Schizothrix rivularioides','(Hansgirg) Forti 1907, Sylloge algarum p. 354',300,'[436]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1983',0,'active','2019-12-17 07:37:42','admin'),(1985,'Hydrocoleum rufescens','Gardner 1927, Mem. New York Bot. Gard. 7: 57-58',211,'[215]','Type no. 972','Species',NULL,'','','','Growing on clay soil, Experiment Station, Mayagüez','[113]',0,1,'',0,'active','2019-12-17 07:38:42','admin'),(1986,'Hydrocoleum stankovicii','Čado 1958, Zbor. rabot. Filos. Fak. Univ. Skopje 5(21)',211,'[382]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-17 07:38:46','admin'),(1987,'Hydrocoleum subcrustaceum','Hansgirg ex Forti 1907, Sylloge algarum p. 323',211,'[436]','','Species',NULL,'','','','freshwater, <span lang=\'en\'><span title=\'\'>mountains </span><span title=\'\'>streams</span></span>; Dalmacia','[53]',0,1,'',0,'active','2019-12-18 11:59:43','admin'),(1988,'Hydrocoleum subhomoeotrichum','&nbsp;Sampaio 1961',211,'','','Species',NULL,'','','','freshwater, wet sandy soils near the river Douro','[82]',0,1,'',0,'active','2019-12-18 11:59:49','admin'),(1989,'Hydrocoleum subincrustaceum','&nbsp;Hansgirg in Kamat 1963, Hydrobiologia 22: 301',211,'[439]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-19 07:54:13','admin'),(1990,'Hydrocoleum terrestre','Novichkova 1960, Bot. mat. Otd. Spor. Rast. Bot. Instit. Komarova, Acad. Nauk SSSR 13:30',211,'[482]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-19 07:54:19','admin'),(1991,'Hydrocoleum turfosum','Voronichin 1923, Bot. Mat. Inst. Spor. Rast. Glav. Bot. Sada 2: 99',211,'[388]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2019-12-19 07:54:29','admin'),(1992,'Dasygloea turfosa','(Voronichin) Angnostidis 2001 ex Komárek &amp; Anagnostidis 2005. Süsswasserflora 19/2, p. 526',168,'[31]','','Species',NULL,'','','','freshwater, among <em>Sphagnum</em> in lakes and swamps, Caucasus','[243]',0,1,'clades:1991',0,'active','2019-12-19 09:01:18','admin'),(1993,'Hydrocoleum violaceum','Martens ex Geitler 1932, Kryptogamen-Flora, p. 1152',1,'[305]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2019-12-19 13:51:07','admin'),(1994,'Trichodesmium clevei','(Schmidt) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 418',334,'[102]','','Species',NULL,'[695]','','','Marine, Gulf of Siam,','[121]',0,1,'',0,'active','2020-01-08 14:12:50','admin'),(1995,'Trichodesmium contortum','(Wille) Brandt 1903, Nordisches Plankton 20: 18',334,'','','Species',NULL,'[696]','','','marine, tropical seas','',0,1,'',0,'active','2020-01-08 14:12:56','admin'),(1996,'Trichodesmium flos-aquae','Ehrenberg 1830',334,'','pre-starting point name','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-01-10 07:20:46','admin'),(1997,'Trichodesmium hildebrandtii','Gomont 1892, Ann. Sci. Nat. Bot., Sér. 7, 16: 197',334,'[235]','','Species',NULL,'[701][702][703][704][705][706]','','','marine, Indian Ocean,','[165]',0,1,'',0,'active','2020-01-10 07:20:59','admin'),(1998,'Trichodesmium iwanoffianum','Nygaard 1926',1,'','','Species',NULL,'','','','freshwater; Sumatra – Lake Toba','[157]',0,1,'',1,'active','2020-01-09 12:36:32','admin'),(1999,'Trichodesmium lacustre','Klebahn 1895',1,'','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-01-09 13:08:46','admin'),(2000,'Trichodesmium lenticulare','(Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 419',334,'[102]','','Species',NULL,'','','','marine, Pacific Ocean (island of Laysan and Hawaii)','[113]',0,1,'Haliarachne lenticularis',0,'active','2020-01-10 08:29:53','admin'),(2001,'Trichodesmium montagnei','Coquerel 1854',334,'','pre-starting point name','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-01-10 13:50:09','admin'),(2002,'Trichodesmium radians','(Wille ex Kirchner) Golubic 1978',334,'','','Species',NULL,'[712]','','','marine','',0,1,'Heliotrichum radians',0,'active','2020-01-10 13:52:06','admin'),(2003,'Trichodesmium scoboideum','Lucas 1919, Proc. Lin. Soc. New South Wales 44: 177-178',334,'[483]','','Species',NULL,'','','','marine; Hope Islands near Cooktown','[121]',0,1,'',0,'active','2020-01-10 13:50:24','admin'),(2004,'Trichodesmium thiebautii','Gomont ex Gomont 1890, J. Botan. 4 (20): 356',334,'[484]','','Species',NULL,'[713][714][715]','','','marine, Atlantic Ocean, Canary Islands, Guadeloupe','',0,1,'',0,'active','2020-01-10 13:50:28','admin'),(2005,'Symplocastrum albaniense','&nbsp;(Drouet) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'','','','','',0,1,'clades:2006',0,'active','2020-01-13 15:06:10','admin'),(2006,'Schizothrix albaniensis','Drouet 1960, Revue Algolog., N. Sér, 5(2): 112',300,'[485]','','Species',NULL,'','','','subaerophytic; on wet limestone rocks in dripping water','[47]',0,1,'',0,'active','2020-01-13 15:05:03','admin'),(2007,'Symplocastrum aurantiacum','(Kützing) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'[717][718][753][754][755]','','','subaerophytic (?), &nbsp;on rocks and woody substrates in stagnant water','[54][60]',0,1,'clades:2034',0,'active','2020-02-24 14:30:30','admin'),(2008,'Microcoleus aurantiacus','Hansgirg 1892,<em>&nbsp;</em>Arch. naturwiss. Landesdurch. Böhmen 8(4): 78',1,'[275]','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>On rocky shores, on the edge of peat swamps</span></span>','',0,1,'',1,'active','2020-01-13 13:16:08','admin'),(2009,'Schizothrix aurantiaca','Kützing 1849, Spec. Algarum, p. 320',300,'[466]','pre-starting point name','Species',NULL,'','','','','',0,0,'',1,'active','2020-02-24 13:32:17','admin'),(2010,'Symplocastrum californicum','(Drouet) Pietrasiak &amp; Johansen in Pietrasiak et al. 2014, Phycologia 53(6): 532',325,'[486]','','Species',NULL,'','BRY37761','WJT9-NPBG9',NULL,NULL,0,1,'clades:2011',0,'active','2020-01-13 15:06:48','admin'),(2011,'Schizothrix californica','Drouet 1943, Am. Midl. Natur. 29(1): 52-53',300,'[487]','','Species',NULL,'','','','&nbsp;in crusts on barren ground','[113]',0,1,'',0,'active','2020-01-13 15:05:17','admin'),(2012,'Symplocastrum flechtnerae','Pietrasiak &amp; Mühlsteinová in Pietrasiak et al. 2014 - Phycologia 53(6): 532',325,'[486]','','Species',NULL,'','BRY37762','WJT32-NPBGF','Desert soils, Cadiz Valley, south of Highway 62, Joshua Tree National Park, San Bernardino County, California','[113]',0,1,'',0,'active','2020-01-13 15:06:55','admin'),(2013,'Symplocastrum torsivum','Pietrasiak &amp; Johansen in Pietrasiak et al. 2014 - Phycologia 53(6): 534',325,'[486]','','Species',NULL,'','BRY37763','CPER-KK1','Short-grass prairie soils, Central Plains Experimental Research site, near Fort Collins, Colorado','[113]',0,1,'',0,'active','2020-01-13 15:07:02','admin'),(2014,'Reptodigitus','Casamatta, Villanueva, Stocks, Vaccarino et Johansen 2020. Journal of Phycology 56: 429',32,'[489]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-08-13 07:21:21','admin'),(2015,'Reptodigitus chapmanii','Casamatta, Villaneuva, Stocks, Vaccarino et Johansen 2020. Journal of Phycology 56:429',2014,'[489]','','Species',NULL,'','CBFS A-117-1','SJR-DC','Epiphytic on <em>Vallisneria alterniflora</em> in fresh or brackish slow-flowing water','[113]',1,1,'',0,'active','2020-08-13 07:22:10','admin'),(2016,'Symplocastrum corticulum','Branco et al. 2006, Algolog. Stud. 121: 25',325,'[490]','','Species',NULL,'','SJRP26907','','tree bark as the margins of the Castores stream, Sao Paulo State','[172]',0,1,'',0,'active','2020-02-14 09:27:38','admin'),(2017,'Symplocastrum parallelum','Branco et al. 2006, Algolog. Stud. 121: 26-27',325,'[490]','','Species',NULL,'','SP365626','','on tree barks, Mata Atlantica, Sao Paulo State','[172]',0,1,'',0,'active','2020-02-14 09:28:20','admin'),(2018,'Symplocastrum silvaticum','Branco et al. 2006, Algolog. Stud. 121: 27, 31',325,'[490]','','Species',NULL,'','SJRP26908','','Atlantic rainforest, Mata Atlantica, Sao Paulo State','[172]',0,1,'',0,'active','2020-02-14 09:28:28','admin'),(2019,'Symplocastrum grunovianum','(Elenkin) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'[721][722][723]','','',NULL,NULL,0,1,'clades:2020',0,'active','2020-02-14 09:28:04','admin'),(2020,'Schizothrix grunoviana','Elenkin 1949, Monographia algarum Cyanophycearum, p. 1733',300,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-02-19 12:01:37','admin'),(2021,'Symplocastrum muelleri','(Nägeli ex Gomont) Anagnostidis 2001, Preslia 73: 371',325,'[9]','','Species',NULL,'[733][734]','','',NULL,NULL,0,1,'clades:559',0,'active','2020-02-18 09:27:38','admin'),(2022,'Symplocastrum naegelii','(Kützing) Anagnostidis 2001, Preslia 73: 371',325,'[9]','basionym: Hypheothrix naegelii','Species',NULL,'[736]','','','Epilithic in streams in central and southern Europe','',0,1,'clades:2036',0,'active','2020-02-25 14:16:46','admin'),(2023,'Symplocastrum penicillatum','(Gomont) Anagnostidis 2001, Preslia 73: 372',325,'[9]','','Species',NULL,'[738][739][741][742][743]','','','Freshwater, in flowing waters, waterfalls and in stony littoral of clear mountain lakes, among mosses','[59]',0,1,'clades:2037',0,'active','2020-02-26 13:18:05','admin'),(2024,'Leibleinia penicillata','Kützing 1847, Bot. Zeit. 5: 194',671,'[492]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-02-18 13:43:57','admin'),(2025,'Symplocastrum purpurascens','(Gomont ex Gomont) Anagnostidis 2001',325,'[9]','','Species',NULL,'[744][745][746]','','','Euterrestrial, subaerophytic, on sandy soils or among mosses','',0,1,'clades:558',0,'active','2020-02-26 13:27:10','admin'),(2026,'Symplocastrum sauterianum','&nbsp;[Grunow in Rabenhorst] Anagnostidis 2001',325,'[9]','','Species',NULL,'[749][748][756]','','','Freshwater, epiphytic on <em>Cladophora glomerata, </em>near Salzburg','[49]',0,1,'clades:2039',0,'active','2020-02-26 14:05:43','admin'),(2027,'Symplocastrum britoniae','Gardner 1932, Sci. Surv. Porto Rico and the Virgin Isl. Volume VIII. Part 2, p. 287',325,'[412]','','Species',NULL,'','','','Growing on mosses, along Catalina-Yunque trail, Luquillo Mts.','[26]',0,1,'',0,'active','2020-02-25 12:24:21','admin'),(2028,'Schizothrix cuspidata','(West &amp; West) West &amp; West 1896',1,'[493]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-02-19 13:15:36','admin'),(2029,'Symploca cuspidata','West et West 1894',324,'[494]','','Species',NULL,'','','','On trees, summit of Trois Pitons','[18]',0,1,'',0,'active','2020-02-25 12:24:12','admin'),(2030,'Schizothrix cuspidata','(West &amp; West) West &amp; West 1896',300,'[493]','','Species',NULL,'[750][751]','','',NULL,NULL,0,1,'clades:2029',0,'active','2020-02-25 12:23:04','admin'),(2031,'Symploca aeruginosa','Setchell et Gardner in Gardner 1918, Univ. Calif. Publ. Bot. 6: 469',324,'[406]','','Species',NULL,'[752]','','','Growing on mud-covered rocks, near the upper tide limit. St. Michael, Alaska','[113]',0,1,'',0,'active','2020-02-25 12:23:31','admin'),(2032,'Symploca atlantica','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16: 109',324,'[235]','','Species',NULL,'','','','marine, along the Atlantic coast','[92]',0,1,'',0,'active','2020-02-25 12:23:55','admin'),(2033,'Symploca borealis','Rabenhorst ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16:&nbsp;',324,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-02-25 12:24:06','admin'),(2034,'Microcoleus aurantiacus','Hansgirg 1892, Arch. naturwis. Landesdurch. Böhmen 8(4): 78',245,'[275]','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>On rocky shores, on the edge of peat swamps, .</span><span title=\'\'>mostly in</span> <span title=\'\'>mountain areas, ŠumavaMts.</span></span>','[54]',0,1,'',0,'active','2020-02-25 12:22:37','admin'),(2035,'Hypheothrix','(Gomont) Kircgner 1898',10,'','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2020-03-03 08:57:42','admin'),(2036,'Hypheothrix naegelii','Kützing ex Gomont 1892, Ann. Sci. Nat., Bot. Sér. 7, 15: 328',2035,'[145]','','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-03-03 08:57:14','admin'),(2037,'Schizothrix penicillata','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 15: 305',300,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-03 08:55:05','admin'),(2038,'Inactis','(Gomont) Kirchner 1898',430,'','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2020-03-03 08:58:25','admin'),(2039,'Inactis sauteriana','Grunow ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 15: 327',2038,'[145]','','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-03-03 08:57:51','admin'),(2040,'Phormidium breve','(Kützing ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 405',267,'[102]','','Species',NULL,'[757][795][796][797][798][799][800][801][802][803][804]','','',NULL,NULL,0,1,'clades:2060',0,'active','2020-03-20 08:53:00','admin'),(2041,'Arthrospira curta','Lemmermann 1908, Arch. Hydrob. Planktonk. 4: 172',108,'[496]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-03 08:53:14','admin'),(2042,'Borzia curta','(Lemmermann) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 370',114,'[102]','','Species',NULL,'[758]','','','Freshwater, known only from marshes of Sicily','[69]',0,1,'clades:2041',0,'active','2020-03-03 08:52:44','admin'),(2043,'Arthrospira desikacharyiensis','Vasishta 1962',108,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2020-03-03 09:01:43','admin'),(2044,'Arthrospira funiformis','Vouk 1915, Yugoslav. Akad. Prirod. Istras. Hrvatski Islavon., Mat. Prirod. 6: 15',108,'','','Species',NULL,'','','','','',0,1,'',0,'active','2020-03-03 14:23:46','admin'),(2045,'Oscillatoria funiformis','(Vouk) Komárek in Anagnostidis 2001, Preslia 73: 375',258,'[9]','','Species',NULL,'[759][760][596]','','','Marine, on rocks, in detritus and among <em>Cladophora </em>and other algae in tide pools along high‑tide level','',0,1,'clades:2044',0,'active','2020-03-03 09:00:53','admin'),(2046,'Purpureonostoc','Cai et Li 2020. Fottea 20(2):111',34,'[497][555]','Originally published as <em>​Purpurea (Fottea 20: 87, 2020)</em>','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-09-16 13:52:58','admin'),(2047,'Purpureonostoc tibetica','Cai et Li 2020. Fottea 20(2):111',2046,'[497][555]','Cai et Li 2020. Fottea 20(1): 88, According to DECIPHER both 16S sequences are chimera','Species',NULL,'','TBCN 201701','CHAB 5880','Free–living on wet soil','[38]',1,1,'',0,'active','2020-09-16 13:54:32','admin'),(2048,'Arthrospira gigantea','(Schmidle) Anagnostidis 1998',108,'','combination missing??','Species',NULL,'[771]','','','planktic, solitary among other algae in stagnant and slow flowing waters, distributed only in the tropics','',0,0,'clades:2049',0,'active','2020-03-05 12:28:22','admin'),(2049,'Spirulina gigantea','&nbsp;Schmidle 1903, Bot. Jahr. Syst. Pflanzenges, Pflanzengeogr. 32: 59',316,'[499]','','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>in a quiet bay of the Mbasi river</span></span>','[232]',0,1,'',0,'active','2020-03-05 12:25:04','admin'),(2050,'Arthrospira gomontiana','Setchell 1895, Bull. Tor. Bot. Club 22: 430',108,'[500]','','Species',NULL,'[772]','','','in a pool of fresh water near Factory Pond in the northern part of Bridgeport, New England','[113]',0,1,'',0,'active','2020-03-06 09:31:30','admin'),(2051,'Arthrospira joshii','Vasishta 1963, J. Ind. Bot. Soc. 42(4): 574',108,'[501]','','Species',NULL,'','','','in a tank near Hoshiarpur','[156]',0,1,'',0,'active','2020-03-09 07:35:41','admin'),(2052,'Arthrospira khannae','Drouet &amp; Strickland in Drouet 1942, Publ. Field Nat. Hist., Bot. Ser. 20(6): 141',108,'[465]','false <em>Arthrospira ghannae</em> Drouet &amp; Strickland in Drouet 1942','Species',NULL,'','type in Cryptogamic Herbarium of Field Museum, No 697','','Planktic in bodies of fresh water; pond near the zoological garden, Rangoon,','[161]',0,1,'',0,'active','2020-03-09 07:36:03','admin'),(2053,'Spirulina laxa','Smith 1916, Bull. Torr. Bot. Club 43: 481',316,'[353]','','Species',NULL,'[775][776]','','','along shore, Soft Lake, Wisconsin','[113]',0,1,'',0,'active','2020-03-13 07:26:38','admin'),(2054,'Arthrospira laxissima','Setchell 1924, Publ. Carnegie Inst. Wash. 341: 183',108,'[502]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-13 07:27:00','admin'),(2055,'Arthrospira leopoliensis','Raciborski 1910, Kosmos 35: 82',108,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-17 12:21:07','admin'),(2056,'Arthrospira margaritae','(Frémy) Gomont ex &nbsp;Komárek &amp; Anagnostidis 2005, Cyanoprokaryota p. 351',108,'[31]','nom. invalid - combination missing','Species',NULL,'[785][786]','','','epiphytic on <em>Calothrix pilosa</em>, described from the coast of Margarita Island','[183]',0,1,'',0,'active','2020-03-18 07:08:50','admin'),(2057,'Arthrospira massartii','Kufferath 1914<em>, </em>Ann. Biol. Lacustre 7: 264&nbsp;',108,'[281]','','Species',NULL,'[787][788]','','','Freshwater, in flowing and stagnant waters, described from a spring','[74]',0,1,'',0,'active','2020-03-18 07:09:23','admin'),(2058,'Spirulina meneghiniana','Zanardini ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 250-251',316,'[235]','','Species',NULL,'[789][790][791][792][793]','','','the western shores at Carteret','[59]',0,1,'',0,'active','2020-03-18 07:09:48','admin'),(2059,'Arthrospira miniata','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 248',1,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-03-17 13:55:22','admin'),(2060,'Oscillatoria brevis','Kützing ex Gomont 1892, Ann. Sci. Nat., Bot., Sér.,7 16:229',258,'[235]','','Species',NULL,'','','','freshwater,&nbsp;','[92][59]',0,1,'',0,'active','2020-03-20 08:52:15','admin'),(2061,'Spirulina nordstedtii','Gomont 1892, Ann. Sci. Nat. Bot., Sér. 7, 16: 252',316,'[235]','','Species',NULL,'[805]','','','salt waters, near Landskrona','[90]',0,1,'',0,'active','2020-03-23 12:04:36','admin'),(2062,'Spirulina subsalsa','Oersted ex Gomont 1892, Ann. Sci. Nat. Bot., Sér. 7, 16: 254',316,'[235]','','Species',NULL,'[806][807][808][809][810][811][812][813][814][815][816][817][818][819][820][821][822]','','','in the salt water, island Fyn; in marine biotopes, and in inland salty and brackish stagnant waters, frequently also in mineral and thermal springs','[55]',0,1,'',0,'active','2020-03-23 12:04:49','admin'),(2063,'Arthrospira okensis','Meyer 1924, Rab. okskoj. biol. stancii 3, 1: 53-57',108,'[513]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-30 07:06:40','admin'),(2064,'Arthrospira pellucida','Wang 1933',108,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2020-03-23 12:02:26','admin'),(2065,'Arthrospira platensis','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 247-248',108,'[235]','','Species',NULL,'[824][825][826][827][828][829]','','','near Montevideo','[182]',0,1,'clades:2066',0,'active','2020-03-23 14:03:10','admin'),(2066,'Spirulina jenneri var. platensis','Nordstedt in Wittrock &amp; Nordstedt 1884, Bot. Notiser 1884: 127',316,'[504]','pre-starting point name&nbsp;','Species',NULL,'','','','near Montevideo','[182]',0,0,'',0,'active','2020-03-24 08:32:36','admin'),(2067,'Arthrospira santannae','Komárek &amp; Komárková-Legnerová 2007, Hoehnea 34(1): 51',108,'[199]','TYPE: BRASIL. RIO DE JANEIRO: Rio de Janeiro, ponds, 13-IX-1996','Species',NULL,'','','SP355964','Planktic, the settling-reservoir near the city of Rio de Janeiro','[172]',0,1,'',0,'active','2020-03-24 08:33:20','admin'),(2068,'Arthrospira setchellii','De Toni 1936, Brescia 1: 5',108,'','unclear species','Species',NULL,'[830]','','',NULL,NULL,0,1,'',0,'active','2020-03-24 08:44:51','admin'),(2069,'Arthrospira skujae','Magrin, Senna &amp; Komárek 1997, Arch. Protistenk. 148(4): 483, 486',108,'[505]','figura typica: figura nostra no. 2B','Species',NULL,'[831]','SP294687','','Freshwater; Porto Velho, Provincia Rondonia','[172]',0,1,'',0,'active','2020-03-24 08:45:05','admin'),(2070,'Arthrospira spirulinoides','Ghose 1924, J. Linn. Soc. (Botany) 46: 338',108,'[459]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-24 08:46:15','admin'),(2071,'Spirulina spirulinoides','(Ghose) Geitler 1925, Die Süsswasser-Flora Deutschlands,p. 344',316,'[296]','','Species',NULL,'[832][834][835]','','',NULL,NULL,0,1,'clades:2070',0,'active','2020-03-24 08:44:24','admin'),(2072,'Spirulina subtilissima','Kützing ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16: 252',316,'[235]','','Species',NULL,'[836][837][838]','','','freshwater; near Abano','[69]',0,1,'',0,'active','2020-03-24 09:29:09','admin'),(2073,'Arthrospira tenuis','Brühl &amp; Biswas 1922, J<em>. Dep. Sci., Univ. Calcutta 4 (1): 7</em>',108,'[506]','','Species',NULL,'[839][840]','','',NULL,NULL,0,1,'',0,'active','2020-03-25 07:09:56','admin'),(2074,'Spirulina versicolor','Cohn ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16: 253',316,'[235]','','Species',NULL,'[841][842][843][844]','','','marine, North Sea, Kiel','[60]',0,1,'',0,'active','2020-03-25 07:11:53','admin'),(2075,'Dasygloea terrestris','(Azevedo) Senna &amp; Komárek 1998, Algolog. Stud. 88',168,'[507]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2076',0,'active','2020-03-30 07:37:17','admin'),(2076,'Lyngbyopsis terrestris','Azevedo 1991, Algolog. Stud. 64: 509',235,'[229]','','Species',NULL,'','','','in soil','[172]',0,1,'',0,'active','2020-03-30 07:36:16','admin'),(2077,'Microcoleus acremannii','Casamatta &amp; Johansen &nbsp;i Casamatta et al. 2005, J. Phycol. 41: 434',245,'[16]','isolated by J. Acreman, originally deposited as Lyngbya sp','Species',NULL,'','BRY C-37703','UTCC313','Sand dunes near Presque’ile, Ontario,','[111]',0,1,'',0,'active','2020-03-30 08:15:11','admin'),(2078,'Microcoleus acutirostris','Gomont 1892, Ann. Sci. Nat., Bot. Sér. 7 15: 352',245,'[145]','','Species',NULL,'[845]','','','Plougastel estuary','[59]',0,1,'',0,'active','2020-03-25 07:08:55','admin'),(2079,'Trichocoleus acutissimus','(Gardner) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'[846][847][848]','','',NULL,NULL,0,1,'clades:2080',0,'active','2020-03-25 08:01:03','admin'),(2080,'Microcoleus acutissimus','Gardner 1927, Mem. NY Bot. Gard. 7: 55-56',245,'[215]','','Species',NULL,'','','','on a church wall, Sabana Grande','[26]',0,1,'',0,'active','2020-03-25 07:57:52','admin'),(2081,'Microcoleus aitchinsonii','Schaarschmidt 1886, J. Linn. Soc. London Bot. 21: 241-242',245,'','pre-starting-point name','Species',NULL,'','','','','[238]',0,0,'',0,'active','2020-03-25 14:04:52','admin'),(2082,'Microcoleus amoenus','(Kützing ex Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013; J. Phycol. 49(6): 1176',245,'[334]','','Species',NULL,'[849][850][851][852][853][854][855][856][857][858][859]','','',NULL,NULL,0,1,'clades:2083',0,'active','2020-03-25 14:04:59','admin'),(2083,'Oscillatoria amoena','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16: 225',258,'[235]','','Species',NULL,'','','','Padova','[69]',0,1,'',0,'active','2020-03-25 14:08:31','admin'),(2084,'Microcoleus amorphus','Wolle ex Drouet 1939,',245,'','','Species',NULL,'[860][861]','','',NULL,NULL,0,1,'',0,'active','2020-03-25 14:05:14','admin'),(2085,'Microcoleus amplus','Gardner 1927, Mem. NY Bot. Gard. 7: 56',245,'[215]','','Species',NULL,'[862]','','','Growing on mud by a stream near Rio Piedras','[26]',0,1,'',0,'active','2020-03-25 14:05:26','admin'),(2086,'Microcoleus anguiformis','Harvey ex Kirchner 1898',245,'','','Species',NULL,'[863]','','',NULL,NULL,0,1,'',0,'active','2020-03-25 14:05:37','admin'),(2087,'Microcoleus annulatus','Fritsch et Rich 1924',245,'','','Species',NULL,'','','','wet soil','',0,1,'',0,'active','2020-03-25 14:05:51','admin'),(2088,'Microcoleus antarcticus','Casamatta &amp; Johansen in Casamatta et al. 2005, &nbsp;J. Phycol. &nbsp;41(2): 434',245,'[16]','isolated by W. Vincent, originally deposited as Phormidium subfuscum Kütz. ex Gom.','Species',NULL,'','BRY C-37702','UTCC474','Benthic substrate of a lake on McMurdo Ice Shelf,','[2]',0,1,'',0,'active','2020-03-30 08:23:06','admin'),(2089,'Microcoleus attenuatus','(Fritsch) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49(6):1176',245,'[334]','','Species',NULL,'[864]','','',NULL,NULL,0,1,'clades:2090',0,'active','2020-03-25 14:06:48','admin'),(2090,'Lyngbya attenuata','Fritsch 1912, Freshwater Algae p. 28',234,'[384]','','Species',NULL,'','','','pond in ice off Black Island, McMurdo Strait, December 31st, 1902','[2]',0,1,'',0,'active','2020-03-25 14:07:50','admin'),(2091,'Microcoleus autumnalis','( Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013',245,'[334]','','Species',NULL,'[865][866][867][868][869][870][871]','','',NULL,NULL,0,1,'',0,'active','2020-03-25 14:07:16','admin'),(2092,'Phormidium autumnale','Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 16: 187',267,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-25 14:08:56','admin'),(2093,'Microcoleus baicalensis','Izhboldina 1984',245,'','','Species',NULL,'','','','Freshwater, on sand, mud, at a depth of 15-20 to 100 m; Lake Baikal','[117]',0,1,'',0,'active','2020-03-25 14:06:29','admin'),(2094,'Microcoleus beggiatoiformis','(Rabenhorst ex Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49(6): 1176',245,'[334]','','Species',NULL,'[872][873][874][875]','','',NULL,NULL,0,1,'clades:2095',0,'active','2020-03-25 14:07:26','admin'),(2095,'Oscillatoria beggiatoiformis','Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 16: 235-236',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-25 14:08:26','admin'),(2096,'Phormidium biasolettianum','Kützing ex Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 16: 190',267,'[235]','','Species',NULL,'[876][877][878][879]','','','At mills near Trieste','[69]',0,1,'',0,'active','2020-03-26 08:00:52','admin'),(2097,'Microcoleus lacustris','Farlow ex Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 15: 359-360',245,'[145]','','Species',NULL,'[918][919]','','','freshwater, near Newton','[113]',0,1,'',0,'active','2020-04-01 07:15:50','admin'),(2098,'Microcoleus burmanicus','(Zeller) Desikachary 1959, Cyanophyta, p. 346',245,'[509]','','Species',NULL,'[905]','','',NULL,NULL,0,1,'synonyms:882',0,'active','2020-03-30 08:45:52','admin'),(2099,'Microcoleus brasiliensis','Borge 1925',245,'','','Species',NULL,'','','','In a lake with rain water','[172]',0,1,'',0,'active','2020-03-26 14:34:06','admin'),(2100,'Microcoleus brebissonii','(Kützing) Hansgirg 1892, Prodromus der Algenflora, p. 79-80',245,'[275]','','Species',NULL,'[880][881]','','',NULL,NULL,0,1,'',0,'active','2020-03-26 14:34:30','admin'),(2101,'Microcoleus burmanicus','Desikachary 1959; Cyanophyta p. 346',245,'[509]','','Species',NULL,'[882]','','',NULL,NULL,0,1,'',1,'active','2020-03-27 06:58:21','admin'),(2102,'Microcoleus calidus','(Gomont ex Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013,J. Phycol. 49(6): 1176',245,'[334]','','Species',NULL,'[883][884][885][886][887]','','',NULL,NULL,0,1,'clades:2103',0,'active','2020-03-26 14:35:35','admin'),(2103,'Phormidium calidum','Gomont ex Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 16: 182',267,'[235]','','Species',NULL,'','','','sulfur thermal, near Cura','[183]',0,1,'',0,'active','2020-03-26 14:33:47','admin'),(2104,'Microcoleus californicus','Drouet 1943, Bot. Ser. Field Mus. Nat. Hist. 20: 167',245,'[473]','TYPE in the Cryptogamic Herbarium of Field Museum','Species',NULL,'','','','In shallow pools of alkaline water, in a cold pool in the travertine quarry, Bridgeport,','[113]',0,1,'',0,'active','2020-03-26 14:35:56','admin'),(2105,'Microcoleus cataractarum','Hansgirg ex Forti 1907 - Sylloge algarum, p. 377',245,'[436]','','Species',NULL,'[888]','','','cold water, near Ljubljana','[87]',0,1,'',0,'active','2020-03-30 06:14:36','admin'),(2106,'Microcoleus caucasicus','(Elenkin et Kosinskaja) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49(6): 1176',245,'[334]','','Species',NULL,'[889]','','',NULL,NULL,0,1,'clades:2107',0,'active','2020-03-30 06:14:57','admin'),(2107,'Oscillatoria terebriformis f. caucasica','Elenkin et Kosinskaja in Elenkin 1949, Monographia algarum p. 1345',258,'[226]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-30 06:12:33','admin'),(2108,'Trichocoleus cavanillesii','(González Guerrero) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2109',0,'active','2020-04-03 12:53:40','admin'),(2109,'Microcoleus cavanillesii','González Guerrero 1946, An. Jard. Bot. Madrid 6(1): 270',245,'[467]','','Species',NULL,'','','','the rivers Ito, San Pedro, Guadalete','[88]',0,1,'',0,'active','2020-03-30 06:15:17','admin'),(2110,'Microcoleus chthonoplastes','Thuret ex Gomont 1892, Ann. Sci. Nat. Bot. Ser. 7, 15. 353-354',245,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-30 06:16:04','admin'),(2111,'Microcoleus codii','Frémy 1932',245,'[510]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-30 06:15:26','admin'),(2112,'Phormidium corium','Gomont ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 172-173',267,'[235]','','Species',NULL,'[893][894][895][896][897][898]','','',NULL,NULL,0,1,'',0,'active','2020-03-30 06:13:57','admin'),(2113,'Microcoleus crustaceus','(Voronichin) Strunecký, Komárek &amp; Johansen in Strunecky et al. 2013',245,'[334]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2114',0,'active','2020-03-30 06:15:33','admin'),(2114,'Phormidium crustaceum','Voronichin 1932, Botan. Žur. 17: 314',267,'[511]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-03-30 06:14:17','admin'),(2115,'Microcoleus cryophilus','Carlson 1913',245,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2020-03-30 06:15:43','admin'),(2116,'Lyngbya curvata','Rabenhorst ex Hansgirg 1892, Prodromus der Algenflora p. 102',234,'[275]','','Species',NULL,'[901][902][903][904]','','','in swamps','',0,1,'',0,'active','2020-03-30 06:12:03','admin'),(2117,'Microcoleus delicatulus','West &nbsp;&amp; West 1896, J. Roy. Microscop. Soc. 16: 164-165',245,'[493]','','Species',NULL,'','','','Glen Tummel, Perthshire, Scotland','[92]',0,1,'',0,'active','2020-03-30 06:15:57','admin'),(2118,'Microcoleus dillwynii','Harvey 1841, A manual of the British algae, p. 169',245,'[512]','pre-starting point name','Species',NULL,'','','','on rocks and stones in the stream, which run through the wood, Penllergaer, Swansea','[92]',0,0,'',0,'active','2020-03-30 06:15:51','admin'),(2119,'Microcoleus erectiusculus','Starmach 1960, Fragm. Flor. Geobot. Polonica 6(4): &nbsp;771',245,'[514]','<span lang=\'en\'><span title=\'\'>fixed material is deposited in Department of Algology PAN Cracow</span></span>','Species',NULL,'','','','<span lang=\'en\'><span title=\'\'>wet</span><span title=\'\'>&nbsp;ground,Góra Parkowa, Krynica</span></span>','[81]',0,1,'',0,'active','2020-03-31 06:09:59','admin'),(2120,'Trichocoleus erectiusculus','(Starmach) Anagnostidis &amp; Komárek in Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2119',0,'active','2020-04-01 06:02:37','admin'),(2121,'Microcoleus evagineus','González Guerrero',245,'','unclear','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 05:58:11','admin'),(2122,'Microcoleus favosus','(Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49: 1176',245,'[334]','','Species',NULL,'[906][907]','','',NULL,NULL,0,1,'clades:2123',0,'active','2020-04-01 05:58:19','admin'),(2123,'Phormidium favosum','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 180-181',267,'[235]','','Species',NULL,'','','','freshwater','',0,1,'',0,'active','2020-04-01 06:02:13','admin'),(2124,'Microcoleus ferrugineus','Frémy 1936, Acta Bot. Inst. Bot. Univ. Zagreb. 11: 61',245,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 05:58:35','admin'),(2125,'Microcoleus fonticola','(Kützing ex Gomont ) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49: 1176',245,'[334]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 05:59:35','admin'),(2126,'Wilmottia murrayi','(West &amp; G.S.West) Strunecký, Elster &amp; Komárek 2011, Fottea 11(1): 62',1,'[132]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-03-31 07:59:42','admin'),(2127,'Microcoleus gracilis','Hassall 1845, A history of the British freshwater algae, p. 261',245,'[515]','pre-starting point name','Species',NULL,'','','','near Aberdeen','[92]',0,0,'',0,'active','2020-04-01 05:59:43','admin'),(2128,'Microcoleus granulatus','Tutin 1940',245,'','unclear','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 06:00:10','admin'),(2129,'Microcoleus guyanensis','Crouan &amp; Crouan in Mazé 1868',245,'[516]','pre-starting point name','Species',NULL,'[908][909]','','',NULL,NULL,0,0,'',0,'active','2020-04-01 06:00:34','admin'),(2130,'Microcoleus hiemalis','(Jaag) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, &nbsp;J. Phycol. 49: 1177',245,'[334]','','Species',NULL,'[910]','','',NULL,NULL,0,1,'clades:2131',0,'active','2020-04-01 06:00:45','admin'),(2131,'Oscillatoria hiemalis','Jaag 1938',258,'[517]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 06:01:49','admin'),(2132,'Trichocoleus hospitus','(Hansgirg ex Gomont) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'[911][913][914]','','',NULL,NULL,0,1,'clades:2133',0,'active','2020-04-01 06:02:42','admin'),(2133,'Microcoleus hospitus','Hansgirg ex Gomont 1892, Ann. Sci. Nat. Bot.,ser. 7, 15: 361',245,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 06:01:06','admin'),(2134,'Microcoleus howellii','Setchell &amp; Gardner 1937, Proceedings of the California Academy of Science, series 4, 22: 71',245,'[518]','Herb. Calif. Acad. Sci., collected by J. T. Howell (413), Apr. 27, 1932','Species',NULL,'','No. 236515','','tide pools at Villamil, Albemarle Island, Galapagos','[174]',0,1,'',0,'active','2020-04-01 06:01:28','admin'),(2135,'Microcoleus hyalinus','(Kützing) Kirchner 1878, Kryptogamen-Flora von Schlesien, p. 244',245,'[519]','pre-starting point name','Species',NULL,'[915]','','','on damp rocks, Teplice nad Metují (Weekelsdorf), Wölfelsfall (Poland)','',0,0,'',1,'active','2020-04-01 07:42:01','admin'),(2136,'Phormidium irriguum','(Kützing ex Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 405',267,'[102]','','Species',NULL,'[916][917]','','',NULL,NULL,0,1,'clades:2137',0,'active','2020-04-01 07:40:09','admin'),(2137,'Oscillatoria irrigua','<em>Kützing ex Gomont 1892, </em>Ann. Sci. Nat., Bot., Sér. 7, 16: 218-219',258,'[235]','','Species',NULL,'','','','freshwater, running water','[59]',0,1,'',0,'active','2020-04-01 07:39:49','admin'),(2138,'Microcoleus ivlevii','Čado 1958, &nbsp;Zbornik Rabot. Filos. Fak. Univ. Skopje, Hydrobioloski Zavod, Ochrid 6(5): 14',245,'[382]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-01 07:34:19','admin'),(2139,'Microcoleus lacustris','(Rabenhorst) Farlow ex Gomont 1892',1,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,1,'active','2020-04-01 07:00:24','admin'),(2140,'Microcoleus hyalinus','(Kützing) Kirchner 1878, Kryptogamen-Flora von Schlesien, p. 244',245,'[519]','pre-starting point name','Species',NULL,'[915]','','','on damp rocks, Teplice nad Metují (Weekelsdorf), Wölfelsfall (Poland)','',0,0,'',0,'active','2020-04-02 05:56:17','admin'),(2141,'Microcoleus lauterbachii','Schmidle 1897, Allgem. bot. Zeitschr. Syst., Floristik, Pflanzeng. 4: 57-58',245,'[520]','','Species',NULL,'','','','freshwater lagoon','[139]',0,1,'',0,'active','2020-04-02 05:57:29','admin'),(2142,'Microcoleus leptodermus','(Kützing) Rabenhorst 1847, Deutschlands Kryptogamen-Flora, p. 76',245,'[521]','pre-starting-point name','Species',NULL,'[920][922][923][924][925]','','',NULL,NULL,0,0,'',0,'active','2020-04-16 11:59:56','admin'),(2143,'Microcoleus limbatus','(Harvey) Bornet 1889, Ackenasy Forschungsreise S.M.S. Gazelle 4: 2',245,'','pre-starting point name','Species',NULL,'[926]','','',NULL,NULL,0,0,'',0,'active','2020-04-16 12:00:37','admin'),(2144,'Phormidium limicola','Kützing 1843, Phycologia generalis p. 192',267,'[135]','syn. Ph. autumale??','Species',NULL,'[927]','','',NULL,NULL,0,0,'',0,'active','2020-04-02 06:00:33','admin'),(2145,'Phormidium lucidum','Kützing ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 179',267,'[235]','','Species',NULL,'[928][929][930]','','','freshwatre, thermal, Karlovy Vary','[54]',0,1,'',0,'active','2020-04-02 06:01:32','admin'),(2146,'Microcoleus lyngbyaceus','Kützing ex Forti 1907',245,'[436]','','Species',NULL,'[931][932][933][934][1014]','','',NULL,NULL,0,1,'',0,'active','2020-04-16 11:44:31','admin'),(2147,'Microcoleus lyngbyei','(Kützing) Crouan &amp; Crouan 1867, Florule du Finistère p. 114',245,'[342]','','Species',NULL,'[935]','','','freshwater','',0,1,'',0,'active','2020-04-02 05:58:53','admin'),(2148,'Microcoleus majusculus','Tseng &amp; Hua in Tseng 1983, Common Seaweeds of China, p. 30',245,'[522]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-02 05:59:03','admin'),(2149,'Microcoleus manshuriense','Noda 1963, &nbsp;J. Fac. Sci. &nbsp;Niigata University, serie 2, 4(3): 112',245,'[523]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-16 12:01:45','admin'),(2150,'Microcoleus maritimus','Bory 1826, Dict. Cl. D´Histoire Naturelle 10: 526',245,'[524]','pre-starting point name','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-04-02 05:59:25','admin'),(2151,'Lyngbya membranacea','(Kützing) Thuret 1875',234,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,0,NULL,0,'active','2020-04-03 05:23:44','admin'),(2152,'Trichocoleus minimus','(Frémy) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2153',0,'active','2020-04-03 12:54:06','admin'),(2153,'Microcoleus minimus','Frémy 1930, Archives de Botanique, Mémoires 3: 82',245,'[221]','','Species',NULL,'','','','stagnant water','[201]',0,1,'',0,'active','2020-04-03 05:24:55','admin'),(2154,'Microcoleus tisserantii','Frémy 1930, Arch. Bot. , Mém. 3(2): 84',245,'[221]','','Species',NULL,'','','','bark of tree','',0,1,'',0,'active','2020-04-03 05:28:22','admin'),(2155,'Microcoleus violaceus','Frémy 1930, &nbsp;Arc. Bot., Mém. 3(2): 81',245,'[221]','','Species',NULL,'','','','subaerophytic, on rock, on siliceous stones','[201]',0,1,'',0,'active','2020-04-03 05:31:37','admin'),(2156,'Microcoleus paludosus','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 15: 358-359',245,'[145]','','Species',NULL,'[937][938][939]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 05:25:20','admin'),(2157,'Oscillatoria pannosa','Bory ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 244',258,'[235]','','Species',NULL,'[940][941][942]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 05:24:10','admin'),(2158,'Microcoleus plantae','(Brüger) Forti 1907, Sylloge Algarum, p. 375-376',245,'[436]','','Species',NULL,'[943]','','','thermal, Bormio','[69]',0,1,'',0,'active','2020-04-03 05:25:45','admin'),(2159,'Trichocoleus polythrix','(Hansgirg) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'[944][945]','','',NULL,NULL,0,1,'clades:2160',1,'active','2020-04-03 12:58:59','admin'),(2160,'Microcoleus polythrix','Hansgirg 1890',245,'[525]','pre-starting point name','Species',NULL,'','','','marine,&nbsp;','',0,0,'',0,'active','2020-04-03 05:26:51','admin'),(2161,'Schizothrix wollei','Drouet 1939, Field Mus. Nat. Hist. Bot. 20: 41',300,'[526]','','Species',NULL,'[946]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 05:30:34','admin'),(2162,'Microcoleus purpureus','Gardner 1927, Mem. NY Bot. &nbsp;Gard. 7: 56-57',245,'[215]','','Species',NULL,'','','','on a wall (a cemetery), in Fort San Cristobal','[26]',0,1,'',0,'active','2020-04-03 05:25:57','admin'),(2163,'Oscillatoria repens','Agardh ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 16: 356',258,'[235]','description in Agardh &nbsp;1824 - Systema algarum. Lundae [Lund]: Literis Berlingianis, p. 61','Species',NULL,'[947][948]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 05:29:16','admin'),(2164,'Phormidium retzii','Gomont &nbsp;ex Gomont 1892, Ann. Sci. Nat., Bot. Sér. 7, 16: 175-176',267,'[235]','','Species',NULL,'[949][950][951][952][953][954]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 05:30:05','admin'),(2165,'Lyngbya rupestris','(Agardh) Hansgirg 1892, Prodromus der Algenflora von Böhmen, p. 105',234,'[275]','','Species',NULL,'[955][956][957][958][959][960]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 13:30:18','admin'),(2166,'Schizothrix rupicola','Tilden 1896, American Algae, p. 153-154',300,'[425]','','Species',NULL,'[961]','','','terrestrial','[113]',0,1,'',1,'active','2020-04-03 13:04:00','admin'),(2167,'Microcoleus rushforthii','Johansen &amp; Casamatta in Casamatta et al. 2005, J. Phycol. 41(2): 433',245,'[16]','','Species',NULL,'','BRY C-37701','UTCC296','spring in Markham, Ontario','[111]',0,1,'',0,'active','2020-04-03 12:34:01','admin'),(2168,'Microcoleus salinus','(Kützing) Montagne in Castagne 1851, p. 113',245,'[528]','pre-starting point name, unclear','Species',NULL,'[1015][1016]','','',NULL,NULL,0,0,'',0,'active','2020-04-16 11:57:52','admin'),(2169,'Microcoleus sampaianus','Sampaio 1941, Bull. de la Soc. Broteriana, Ser. 2, 5: 11',245,NULL,NULL,'Species',NULL,NULL,'','','','[82]',0,1,NULL,0,'active','2020-04-03 12:34:12','admin'),(2170,'Trichocoleus sanctae-crucis','(Frémy) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2171',0,'active','2020-04-03 12:32:39','admin'),(2171,'Microcoleus sanctae-crucis','Frémy 1939, Dansk. Bot. Ark. 9 (7): l7',245,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:34:23','admin'),(2172,'Microcoleus setchellianus','(Gomont) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, &nbsp;J. Phyc. 49(6): 1177',245,'[334]','','Species',NULL,'[962]','','',NULL,NULL,0,1,'clades:2173',0,'active','2020-04-03 12:34:44','admin'),(2173,'Phormidium setchellianum','Gomont 1892, Ann. Sci. Nat., Bot. Sér. 7, 16: 190',267,'[235]','','Species',NULL,'','','','benthic, on stones, Connecticut','[113]',0,1,'',0,'active','2020-04-03 12:31:58','admin'),(2174,'Microcoleus sikkimensis','Santra 1984',245,'[529]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:35:00','admin'),(2175,'Microcoleus sinensis','Jao 1939, Sinensia 10: 191',245,'[530]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:35:09','admin'),(2176,'Trichocoleus sociatus','(West &amp; West) Anagnostidis 2001, Preslia 73:&nbsp;',333,'[9]','','Species',NULL,'[963]','','',NULL,NULL,0,1,'',1,'active','2020-04-03 12:58:40','admin'),(2177,'Microcoleus sociatus','West &amp; West 1897, J. Bot. , Brit. &nbsp;Forein 35: 271',245,'[370]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:35:20','admin'),(2178,'Microcoleus steenstrupii','Boye-Petersen 1923, Arbej. Bot. København 101(7): 292',245,'[427]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:35:29','admin'),(2179,'Microcoleus subandinus','Schwabe 1944',245,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2020-04-03 12:35:36','admin'),(2180,'Microcoleus subsalsus','(Gomont) Strunecky, Komárek et Johansen in Strunecky et al. 2013',245,'[334]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2181',0,'active','2020-04-03 12:35:46','admin'),(2181,'Phormidium subsalsum','Gomont 1899, Bull. Soc. Bot. France 46: 38',267,'[224]','','Species',NULL,'','','','salt water, Alsatahag','[80]',0,1,'',0,'active','2020-04-03 12:32:07','admin'),(2182,'Microcoleus subtorulosus','Gomont ex Gomont 1892, Ann. Sci. Nat., Bot. Sér. 7, 15: 360',245,'[145]','','Species',NULL,'[964][965][966][967][968][969]','','','freshwater, rivers near Lund','[90]',0,1,'',0,'active','2020-04-03 12:35:54','admin'),(2183,'Trichocoleus tenerrimus','(Gomont) Anagnostidis 2001, Preslia 73: 355',334,'[9]','','Species',NULL,'[970][971][972]','','',NULL,NULL,0,1,'clades:2184',0,'active','2020-04-03 12:49:30','admin'),(2184,'Microcoleus tenerrimus','Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7, 15: 355',245,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:36:05','admin'),(2185,'Microcoleus terrestris','(Desmazières) Thuret ex Hansgirg 1892; Prodromus der Algenflora p. 76',245,'[275]','','Species',NULL,'[973][974]','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:36:15','admin'),(2186,'Microcoleus thermalis','Vouk 1916, Jugoslav. Akad. Prir. Istraz. Hrvatske i Slavonije 8: 12',245,'[531]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:36:25','admin'),(2187,'Trichocoleus thermalis','(Vouk) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2186',1,'active','2020-04-03 12:58:23','admin'),(2188,'Microcoleus thomensis','Sampaio 1958, Minostr. do Ultramar. Lisboa, Estud., Ens. &amp; Doc. 47: 27',245,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 12:36:35','admin'),(2189,'Schizothrix rupicola','Tilden 1896',300,'[425]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-03 13:33:17','admin'),(2190,'Trichocoleus voukii','&nbsp;(Frémy) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2191',0,'active','2020-04-12 10:01:31','admin'),(2191,'Microcoleus voukii','Frémy 1932, Com. Rendu Hebdom. &nbsp;Séan.\'Acad. Sci.195: 1413-1414',245,'[510]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-12 09:59:20','admin'),(2192,'Trichocoleus wuitneri','(Frémy ex Frémy) Anagnostidis 2001, Preslia 73: 369',333,'[9]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2193',0,'active','2020-04-12 10:01:59','admin'),(2193,'Microcoleus wuitneri','Frémy 1932, Com. Rendu Hebdom. Séan. Acad. Sci. 195: 1413',245,'[510]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-12 09:59:57','admin'),(2194,'Microcoleus vulgaris','(Kützing ex Gomont ) Strunecky, Komárek &amp; Johansen in Strunecky et al. 2013, J. Phycol. 49(6): 1177',245,'[334]','','Species',NULL,'[993][994][995][996][997][998][999][1000][1001][1002]','','',NULL,NULL,0,1,'clades:2195',0,'active','2020-04-12 09:59:30','admin'),(2195,'Phormidium vulgare','Kützing 1843, Phycologia generalis p. 193',267,'[135]','pre-starting-point name','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2020-04-13 15:52:34','admin'),(2196,'Microcoleus wallrothii','Strunecký, Komárek &amp; Johansen in Strunecký et al. 2013, J. Phycol. 49: 1177',245,'[334]','','Species',NULL,'[1003][1004][1005]','','',NULL,NULL,0,1,'clades:2197',0,'active','2020-04-12 09:59:42','admin'),(2197,'Oscillatoria violacea','Wallroth ex Gomont 1892, Ann. Sci. Nat., Bot., Sér. 7 16: 240',258,'[235]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-12 10:01:13','admin'),(2198,'Microcoleus weeksii','Setchell &amp; Gardner in Gardner 1918, Univ. Calif. Publ. Bot. 6: 470',245,'[406]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-12 09:59:49','admin'),(2199,'Microcoleus furcatus','(Rabenhorst) Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 79',245,'[275]','','Species',NULL,'[1013]','','',NULL,NULL,0,1,'',0,'active','2020-04-16 11:40:17','admin'),(2200,'Cyanoplacoma regulare','(Broady et Ingerfeld) Molinari &amp; Guiry 2021. Notulae Algarum 183:2',19,'[532][621]','','Species',NULL,'[1047]','CHR 379746','','first orders streams, colonies attached to stable rock surfaces and bryophytes','[134]',0,1,'',1,'active','2022-08-11 13:54:35','admin'),(2201,'Synechococcus salsus','H.-R. Lv et S.-L. Xie',326,'[533]','holotype insufficiently defined (only herbarium code mentioned)','Species',NULL,'','SXU','','salt lake','[38]',0,0,'',0,'active','2020-04-14 12:32:54','admin'),(2202,'Violetonostoc','F. Cai et R. Li 2020. Algae 35(1): 3',34,'[534]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-04-16 09:57:17','admin'),(2203,'Violetonostoc minutum','F. Cai et R. Li 2020. Algae 35(1): 3',2202,'[534]','','Species',NULL,'','HBI SSSA201402','CHAB 5840','Free-living on rocky substrates (cloudy, subtropical humid monsoon climate)','[38]',1,1,'',0,'active','2020-04-16 09:56:50','admin'),(2204,'Cyanothece svehlovae','Mareš, J.R. Johansen et Hauer 2019. Journal of Phycology 55: 597',164,'[397]','','Species',NULL,'','CBFS A098-1','NIVA-CYA 258/1','Polar terrestrial habitat. Lichen vegetation growing on gravel','[2]',0,1,'',0,'active','2020-04-16 09:33:41','admin'),(2205,'Gloeothece aequatorialis','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 598',192,'[397]','','Species',NULL,'','CBFS A-010-1','SAG 36.87','Wet stony wall, gneiss, tropical biome','[190]',0,1,'',0,'active','2020-04-16 09:34:07','admin'),(2206,'Gloeothece aurea','Mareš, Hauer et J.R. Johansen 2019. Journal of Phycology 55: 598',192,'[397]','','Species',NULL,'','CBFS A-080-1','CCALA 1111','Calcareous stone surface, tropical rainforest.','[100]',0,1,'',0,'active','2020-04-16 09:34:42','admin'),(2207,'Gloeothece bryophila','J. R. Johansen 2019. Journal of Phycology 55: 598',192,'[397]','','Species',NULL,'','CBFS A-101-1','HA4964-KK2','Growing among mosses and liverworts on a wet lava wall, tropical island biome.','[113]',0,1,'',0,'active','2020-04-16 09:35:17','admin'),(2208,'Gloeothece citriformis','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 599',192,'[397]','','Species',NULL,'','CBFS A-69-1','PCC 7424','Soil of a rice field, tropical biome.','[224]',0,1,'',0,'active','2020-04-16 09:35:33','admin'),(2209,'Aphanocapsa membranacea','Rabenhorst 1865',105,'[438]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-16 09:33:10','admin'),(2210,'Gloeothece membranacea','(Rabenhorst) Bornet 1892',192,'[397][535]','','Species',NULL,'','neotype CBFS A-105-1','SAG 26.84=PCC6501',NULL,NULL,0,1,'clades:2209',0,'active','2020-04-16 09:36:43','admin'),(2211,'Gloeothece reniformis','Mareš, Hauer et J.R. Johansen',192,'[397]','','Species',NULL,'','CBFS A-097-1','CCALA 1113','Volcanic stone surface, tropical island','[113]',0,1,'',0,'active','2020-04-16 09:36:57','admin'),(2212,'Gloeothece fuscolutea','Nägeli 1849',192,'[115]','','Species',NULL,'','L0055243','',NULL,NULL,1,1,'',0,'active','2020-04-16 09:36:15','admin'),(2213,'Gloeocapsa tepidariorum','A. Braun in Rabengorst 1865',190,'[438]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-04-17 06:27:24','admin'),(2214,'Gloeothece tepidariorum','(A. Braun in Rabenhorst) Lagerheim 1883:44',192,'[397]','','Species',NULL,'','neotype CBFS A-104-1','CCALA 1112',NULL,NULL,0,1,'clades:2213',0,'active','2020-04-17 06:27:52','admin'),(2215,'Gloeothece tonkinensis','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 600',192,'[397]','','Species',NULL,'','Figure 11, a–f in Mareš et al. 2019','Viet Nam 01','Rice field, tropical biome.','[168]',0,1,'',0,'active','2020-04-17 06:28:08','admin'),(2216,'Gloeothece verrucosa','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 601',192,'[397]','','Species',NULL,'','CBFS A-071-1','PCC 7822','Soil of rice fields, tropical biome','[156]',0,1,'',0,'active','2020-04-17 06:28:28','admin'),(2217,'Crocosphaera subtropica','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 602',140,'[397]','','Species',NULL,'','CBFS A-078-1','ATCC 51142','Subtropical ocean, intertidal area.','[113]',0,1,'',0,'active','2020-04-17 06:29:04','admin'),(2218,'Crocosphaera chwankensis','Mareš et J.R. Johansen 2019. Journal of Phycology 55: 602',140,'[397]','','Species',NULL,'','CBFS A-079-1','CCY 0110','Marine sediment, tropical ocean','',0,1,'',0,'active','2020-04-17 06:28:53','admin'),(2219,'Microcoleus heterotrichus','[Kützing] Wolle ex Hansgirg 1892, Arch. naturwiss. Landesdurchf. Böhmen 8(4): 79',1,'[275]','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-04-16 11:49:16','admin'),(2220,'Planktothrix spiroides','Wang &amp; Li in Liu &amp; al. 2013, Phycologia 52(4): 328',1,'','','Species',NULL,'','','',NULL,NULL,0,1,'',1,'active','2020-04-17 11:12:13','admin'),(2221,'Stenomitos kolaensis','Shalygin, Shalygina et Johansen',481,'[539]','','Species',NULL,'','KPABG (C) 4182','Pasv RS28','Al-Fe humic podzol soil in a young boreal forest composed of coniferous and deciduous trees','[117]',0,1,'',0,'active','2020-04-24 10:40:53','admin'),(2222,'Stenomitos hiloensis','Johansen, Gargass et Shalygin 2020. Phytotaxa 440(2): 114',481,'[539]','','Species',NULL,'','BISH 776187','HA6792-KK3','Seep wall in tropical rain forest','[113]',0,1,'',0,'active','2020-04-24 10:40:32','admin'),(2223,'Cyanobacterium aponinum','Moro, Rascio, La Rocca, Di Bella et Andreoli 2007. Algological Studies 123: 9',144,'[540]','does not meet ICN/ICNP rules for holotypes/type strains; the genus is not valid','Species',NULL,'','','PCC 10605','cyanobacterial mat covering thermal mud, water temperature 40 C, pH 6,8','[69]',0,0,'',0,'active','2020-05-06 08:04:23','admin'),(2224,'Chroococcidiopsis cyanosphaera','Komárek et Hindák 1975. Arch. Hydrobiol./Algological Studies 13: 320',660,NULL,NULL,'Species',NULL,NULL,'','Hindák 1965/25, Hindák 1962/26','periphytic in mineral springs and pools','[16]',0,1,NULL,0,'active','2020-05-06 08:03:34','admin'),(2225,'Nodosilinea svalbardensis','Davydov et Shalygin 2020. Phytotaxa 442(2): 64',565,'[541]','','Species',NULL,'','KPABG 3220','LID-610001','Sand wetlands, an upper surface of the sand.','[89]',0,1,'',0,'active','2020-05-14 12:11:44','admin'),(2226,'Oculatella cataractarum','Bohunická et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 457',478,'[547]','','Species',NULL,'','BRY37749','CCALA 1038, CCALA 1039','Wet sandstone seep wall among other algae in semi-arid shrub-steppe','[113]',0,1,'',0,'active','2020-05-27 11:35:01','admin'),(2227,'Oculatella hafnerensis','Kováčik et Johansen 2014. Eur. J. Phycol. 49(4): 460',478,'[547]','','Species',NULL,'','BRY37751','CCALA 1047','suspended benthos of a temperate lake','[49]',0,1,'',0,'active','2020-05-27 12:20:37','admin'),(2228,'Oculatella neakameniensis','Kováčik et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 460',478,'[547]','','Species',NULL,'','BRY37752','CCALA 1042','Semi-arid volcanic soil','[62]',0,1,'',0,'active','2020-05-27 12:20:52','admin'),(2229,'Oculatella mojaviensis','Pietrasiak et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 461',478,'[547]','','Species',NULL,'','BRY37754','CCALA 1044','Dolomitic soils in hot desert of North America.','[113]',0,1,'',0,'active','2020-05-27 12:20:42','admin'),(2230,'Oculatella coburnii','Pietrasiak et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 462',478,'[547]','','Species',NULL,'','BRY37757','CCALA 1046','Granitic soils in hot desert of North America.','[113]',0,1,'',0,'active','2020-05-27 12:20:26','admin'),(2231,'Oculatella atacamensis','Osorio-Santos et Johansen in Osorio-Santos et al. 2014. Eur. J. Phycol. 49(4): 463',478,'[547]','','Species',NULL,'','BRY37758','CCALA 1047','Soils and under diaphanous (quartz) rocks at the rock-soil interface in the Atacama Desert.','[178]',0,1,'',0,'active','2020-05-27 12:20:13','admin'),(2232,'Wilmottia koreana','N. Lee, Y. Seo, J. Ki et O. Lee 2020. Phytotaxa 447(4): 242',343,'[548]','','Species',NULL,'','NIBRCY0000001018','FBCC-A812 (=ACKU585)','tree bark','[40]',0,1,'',0,'active','2020-06-17 06:01:07','admin'),(2233,'Nostoc neudorfense','P. Singh, Šnokhousová et Elster 2020. IJSEM70: 2748',255,'[549]','','Species',NULL,'','CCALA 1121 (metabolically inactive strain)','CCALA 1121','seepage/wet soil','[54]',0,1,'',0,'active','2020-07-15 12:35:45','admin'),(2234,'Fortiea necridiiformans','Saraf, Dawda, Suradkar, Agre et P. Singh 2020. IJSEM',182,'[550]','','Species',NULL,'','GCC 20206 (metabolically inactive)','PS4G','Saraf et al. 2020: Bluish-green mat growing luxuriantly in soil constantly seeped by the water from the adjoining freshwater lake. The sampling site was also surrounded by small stones. The temperature at the time of sample collection was 27 °C and the pH','[156]',0,1,'',0,'active','2020-08-13 07:57:50','admin'),(2235,'Cyanocohniella crotaloides','P. Jung, Mikhailyuk, Emrich, Dultz et Büdel 2020. Journal of Phycology',709,'[551]','','Species',NULL,'','HBG024670','DSM 109255 = SAG 2592','beach mat','[79]',0,1,'',0,'active','2020-08-13 07:57:31','admin'),(2236,'Oculatella crustae-formantes','P. Jung, Mikhailyuk, Emrich, Dultz et Büdel 2020. Journal of Phycology',478,'[551]','','Species',NULL,'','HBG 024671','DSM 109267 = SAG 2593','Biological soil crusts','[80]',0,1,'',0,'active','2020-08-13 07:56:48','admin'),(2237,'Aliterella chasmolithica','P. Jung, Mikhailyuk, Emrich, Dultz et Büdel 2020. Journal of Phycology',466,'[551]','','Species',NULL,'','HBG 024669','DSM 109265 = SAG NA2019.003','Chasmolithic in boulders of granite','[178]',0,1,'',0,'active','2020-08-13 07:57:15','admin'),(2238,'Westiellopsis akinetica','Mishra et P. Singh 2020. FEMS Microbiology Letters 367 (5): fnaa046, p. 8',342,'[552]','','Species',NULL,'','GCC 20191 (metabolically inactive culture)','SNS 3','Mishra et al. 2020: Growing as dark green mats on the soil in the SNPG garden in between dense shade of small herbaceous plants. The soil surrounding the mats had organic debris along with fine particles of stone and sand. The pH of the soil was found to','[156]',0,1,'',0,'active','2020-08-14 11:18:19','admin'),(2239,'Dictyophoron','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 455',32,'[553]','','Genus',NULL,'',NULL,NULL,'','[95]',0,1,NULL,0,'active','2020-08-21 13:46:35','admin'),(2240,'Dictyophoron claviapex','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 455',2239,'[553]','','Species',NULL,'','iconotype Fig. 8','',NULL,NULL,1,1,'',0,'active','2020-08-21 13:47:00','admin'),(2241,'Gloeotrichia aurantiaca','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 465',193,'[553]','','Species',NULL,'','iconotype Fig. 15a','','','[95]',0,1,'',0,'active','2020-08-24 06:16:34','admin'),(2242,'Hassallia maya','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 468',200,'[553]','','Species',NULL,'','iconotype Fig. 18a','',NULL,NULL,0,1,'',0,'active','2020-08-24 06:16:07','admin'),(2243,'Nodularia aggregata','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 471',254,'[553]','','Species',NULL,'','iconotype Fig. 19','','','[95]',0,1,'',0,'active','2020-08-24 06:15:51','admin'),(2244,'Scytonema belizensis','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 473',302,'[553]','','Species',NULL,'','iconotype Fig. 21','','','[95]',0,1,'',0,'active','2020-08-24 06:15:04','admin'),(2245,'Stigonema eliskae','Komárek et Komárková 2017. Nova Hedwigia 105: 477',321,'[553]','','Species',NULL,'','iconotype Fig. 24','','','[95]',0,1,'',0,'active','2020-08-24 06:14:35','admin'),(2246,'Tolypothrix caribica','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 479',332,'[553]','','Species',NULL,'','iconotype Fig. 27','',NULL,NULL,0,1,'',0,'active','2020-08-24 06:13:44','admin'),(2247,'Anabaena lutea','Gardner 1927. Mem. New Yourk Bot. Garden7: 58',102,'[215]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-08-24 06:17:20','admin'),(2248,'Trichormus luteus','Komárek, Komárková, Ventura, Kozlíková-Zapomělová et Rejmánková 2017. Nova Hedwigia 105(3-4): 481',335,'[553]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2247',0,'active','2020-08-24 06:15:29','admin'),(2249,'Croatella','Ercegović 1925. Acta Bot. Univ. Zagreb 1: 91',40,'[83]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-08-24 06:13:20','admin'),(2250,'Croatella lithophila','Ercegović 1925. Acta Bot. Univ. Zagreb 1: 91',2249,'[83]','','Species',NULL,'','','','on surface of wet rocks among other cyanobacteria','[53]',1,1,'',0,'active','2020-08-24 06:59:26','admin'),(2251,'Cylindrospermum rectangulare','Playfair 1915. Proceedings if the Linnean Society of New South Wales 40: 349',166,'[379]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2020-08-24 08:18:02','admin'),(2252,'Johannesbaptistia floridana','Berthold &amp; Laughinghouse IV 2020. Fottea 20(2): 153',219,'[554]','','Species',NULL,'','US 227647','BLCC-M67','Marine sediment','[113]',0,1,'',0,'active','2020-09-16 14:13:33','admin'),(2253,'Oculatella dilatativagina','Becerra-Absalón et Johansen 2020. Fottea 20(2): 164',478,'[556]','','Species',NULL,'','FCME CB18','UAM 687, according to GenBank UAM 426','Aerophytic, forming surface biocrust from semi–desert soils','[100]',0,1,'',0,'active','2020-09-16 14:13:57','admin'),(2254,'Oculatella leona','Becerra-Absalón et Johansen 2020. Fottea 20(2): 165',478,'[556]','','Species',NULL,'','FCME CB2','UAM710, according to GenBank UAM 427','Aerophytic, in biocrusts with other species from semi–desert soils','[100]',0,1,'',0,'active','2020-09-16 14:14:14','admin'),(2255,'Pseudanabaena cinerea','Tuji et Niiyama 2018. Phycological research 66: 293',282,'[557]','','Species',NULL,'','TNS AL-58685','NIES-4065','plankton in lakes and reservoirs','[39]',0,1,'',0,'active','2020-09-21 05:59:18','admin'),(2256,'Pseudanabaena yagii','Tuji et Niiyama 2018. Phycological research 66: 294',282,'[557]','','Species',NULL,'','TNS AL-58682','NIVA-CYA 111','lake plankton','',0,1,'',0,'active','2020-09-21 05:59:33','admin'),(2257,'Laspinemaceae','Zimba, Shalygin et Huang 2020. Phycologia',10,'[558]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-10-13 06:48:35','admin'),(2258,'Perforafilum','Zimba, Shalygin et Huang 2020. Phycologia',2257,'[558]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2020-10-13 06:48:24','admin'),(2259,'Perforafilum tunneli','Zimba, Shalygin et Huang 2020. Phycologia',2258,'[558]','','Species',NULL,'','PH00172109','PZ1','microbial mat within wind-tidal sand flats (Zimba et al. 2020)','[113]',1,1,'',0,'active','2020-10-13 06:48:19','admin'),(2260,'Parakomarekiella','Soares, Ramos et Portugal 2020. European Journal of Phycology',34,'[559]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-01-07 13:57:50','admin'),(2261,'Parakomarekiella sesnandensis','Soares, Ramos et Portugal 2020. European Journal of Phycology',2260,'[559]','','Species',NULL,'','COI 00088998','ULC591','artificial limestone wall','[82]',1,1,'',0,'active','2021-01-07 14:07:53','admin'),(2262,'Xenococcus spongiosum','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 5',347,'[560]','','Species',NULL,'','TAU A01004','TAU-MAC 0615T','Rocky reef of the sublittoral zone, at a depth of 9.8 m; found to live in association with the sponge Ircinia variabilis','[62]',0,1,'',0,'active','2021-02-19 12:10:17','admin'),(2263,'Rhodoploca','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',2545,'[560]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:36:30','admin'),(2264,'Rhodoploca sivonenia','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',2263,'[560]','','Species',NULL,'','ΤAU A01005','TAU-MAC 1815T','Rocky reef of the sublittoral zone at a depth of 9.6 m; in association with the sponge Agelas oroides.','[62]',1,1,'',0,'active','2021-05-07 07:06:32','admin'),(2265,'Cymatolege','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',2545,'[560]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:35:51','admin'),(2266,'Cymatolege spiroidea','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',2265,'[560]','','Species',NULL,'','ΤAU A01006','TAU-MAC 1315T','Rocky reef of the sublittoral zone at a depth of 6.8 m; found to live in association with the sponge Aplysina aerophoba.','[62]',1,1,'',0,'active','2021-05-07 07:06:23','admin'),(2267,'Cymatolege isodiametrica','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',2265,'[560]','','Species',NULL,'','ΤAU A01007','TAU-MAC 1715T','Rocky reef of the sublittoral zone at a depth of 21 m; found to live in association with the sponge Hexadella racovitzai','[62]',0,1,'',0,'active','2021-05-07 07:06:17','admin'),(2268,'Metis','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 6',1034,'[560]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 07:26:00','admin'),(2269,'Metis fasciculata','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 7',2268,'[560]','','Species',NULL,'','ΤAU A01008','TAU-MAC 1415T','Sublittoral zone at a depth of 21 m; found to live in association with the sponge Axinella damicornis.','[62]',1,1,'',0,'active','2021-05-07 07:25:47','admin'),(2270,'Aegeococcus','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 7',2526,'[560]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:34:42','admin'),(2271,'Aegeococcus anagnostidisii','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 7',2270,NULL,NULL,'Species',NULL,NULL,'ΤAU A01009','TAU-MAC 0815T','Overhang of the sublittoral zone at a depth of 21 m; found to live in association with the sponge Axinella damicornis.','[62]',1,1,NULL,0,'active','2021-05-07 07:50:59','admin'),(2272,'Aegeococcus thuretii','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 11',2270,'[560]','','Species',NULL,'','ΤAU A01010','TAU-MAC 2015T','Rocky reef of the sublittoral zone at a depth of 19.3 m; found to live in association with the sponge Stryphnus ponderosus.','[62]',0,1,'',0,'active','2021-05-07 07:51:05','admin'),(2273,'Thalassoporum','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 11',2527,'[560]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:36:54','admin'),(2274,'Thalassoporum komareki','Konstantinou et Gkelis 2021. Molecular Phylogenetics and Evolution 155, 106991, p. 11',2273,'[560]','','Species',NULL,'','ΤAU A01011','TAU-MAC 1515T','Rocky reef of the sublittoral zone at a depth of 9.8 m; found to live in association with the sponge Spirastrella cunctatrix.','[62]',1,1,'',0,'active','2021-05-07 07:50:34','admin'),(2275,'Pseudochroococcus','Duval, Hamlaoui et Bernard 2021. FEMS Microbes 2: xtab006, p. 4',16,'[561]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 09:06:00','admin'),(2276,'Pseudochroococcus coutei','Duval, Hamlaoui et Bernard 2021. FEMS Microbes 2: xtab006, p. 4',2275,'[561]','','Species',NULL,'','PMC 885.14 formaldehyde-fixed, cryopreserved','PMC 885.14','Epilithic biofilm, retention basin of the thermal springs.','[59]',1,1,'',0,'active','2021-05-07 09:05:44','admin'),(2277,'Trichotorquatus','Pietrasiak et Johansen 2021. Journal of Phycology , p 4',1034,'[562]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 11:30:15','admin'),(2278,'Trichotorquatus maritimus','Pietrasiak, Reeve et Johansen 2021. Journal of Phycology , p 4',2277,'[562]','','Species',NULL,'','NMC 109455','SMER-A','Biological soil crusts in coastal sage scrub.','[113]',1,1,'',0,'active','2021-05-07 11:30:05','admin'),(2279,'Trichotorquatus coquimbo','Osorio-Santos, Pietrasiak et Johansen 2021. Journal of Phycology , p 7',2277,'[562]','','Species',NULL,'','NMC 109461','ATA2-1- KO25A','Biological soil crust.','[178]',0,1,'',0,'active','2021-05-07 11:29:56','admin'),(2280,'Trichotorquatus andrei','Pietrasiak et Johansen 2021. Journal of Phycology , p 9',2277,'[562]','','Species',NULL,'','NMC 109459','WJT9-NPBG15','Sandy, gravelly soil from mixed parent material, algal and lichen crust present but not common, plants present.','[113]',0,1,'',0,'active','2021-05-07 11:29:51','admin'),(2281,'Trichotorquatus ladouxae','Pietrasiak et Johansen 2021. Journal of Phycology , p 10',2277,'[562]','','Species',NULL,'','NMC 109456','WJT36-NPBG11','Sandy, gravelly soil from granitic outcrops, plants and well-developed algal crusts.','[113]',0,1,'',0,'active','2021-05-07 11:30:01','admin'),(2282,'Neochroococcus','R. Geng et G. Yu 2021. Fottea 21(1): 46',16,'[563]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 11:58:58','admin'),(2283,'Neochroococcus gongqingensis','R. Geng et G. Yu 2021. Fottea 21(1): 46',2282,'[563]','','Species',NULL,'','HBI JXGQ201806','CHAB 4018','Free–living in freshwater channels','[38]',1,1,'',0,'active','2021-05-07 11:58:36','admin'),(2284,'Brasilonema fioreae','Berthold, Barbosa, Lefler et Laughinghouse 2021. Fottea 21(1): 84',118,'[564]','','Species',NULL,'','US227704','LCC–T72','In greenhouses attached to walls, rocks, and planters.','[113]',0,1,'',0,'active','2021-05-07 12:31:52','admin'),(2285,'Brasilonema santannae','Berthold, Barbosa, Lefler et Laughinghouse 2021. Fottea 21(1): 84',118,NULL,NULL,'Species',NULL,NULL,'US227696','BLCC–T43=ULC544','Walls, rocks and planters in greenhouses.','[113]',0,1,NULL,0,'active','2021-05-07 12:32:09','admin'),(2286,'Brasilonema wernerae','Berthold, Barbosa, Lefler et Laughinghouse 2021. Fottea 21(1): 84',118,NULL,NULL,'Species',NULL,NULL,'US227697','BLCC–T49=ULC573','Subaerophytic and terrestrial.','[113]',0,1,NULL,0,'active','2021-05-07 12:31:29','admin'),(2287,'Geminocystaceae','Tuji, Yamaguchi et Niiyama 2021. Fottea 21(1): 102',6,'[565]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-07 12:28:52','admin'),(2288,'Annamia dubia','Tuji, Yamaguchi et Niiyama 2021. Fottea 21(1): 102',611,'[565]','','Species',NULL,'','TNS AL–58964','NIES–4383','Plankton in lakes','[39]',0,1,'',0,'active','2021-05-07 12:29:27','admin'),(2289,'Mastigocladus ambikapurensis','Jaiswal et Singh 2021. Plant Systematics and Evolution 307: 33 p. 10',239,'[566]','','Species',NULL,'','GCC 20207','GCC 20207 (TA-9)','Jaiswal et al. (2021): TA-9 was isolated from a hot spring having temperature around 52 °C and pH 8.2. The salinity, total dissolved solids, conductivity and alkalinity were measured on-site with the values being 324 ppm, 475 ppm, 668 μS cm<sup>−1</sup> a','[156]',0,1,'',0,'active','2021-05-13 08:55:35','admin'),(2290,'Symphyonema bifilmentata','Jung, Büdel et Lakatos 2021. Microbes 9:745, p. 5',322,'[567]','','Species',NULL,'','HBG 024930','DSM 112338 = CCAP 1427/4','shallow soil deepening that was every then and now wet','[91]',0,1,'',0,'active','2021-05-13 09:22:19','admin'),(2291,'Iningainema tapete','Berthold et Laughinghouse 2021. Harmful Algae 101: 101969, p. 3',613,'[568]','','Species',NULL,'','US 227647','BLCC-T55','subaerial and terrestrial','[113]',0,1,'',0,'active','2021-05-13 11:41:03','admin'),(2292,'Iningainema sahyadrensis','Maltsev et Kulikovskiy 2021. European Journal of Phycology 2021',613,'[570]','','Species',NULL,'','AHMA MZ-Iac9','Iac9','Wet rocky wall in tropical region','[156]',0,1,'',0,'active','2021-05-14 10:26:04','admin'),(2293,'Vermifilaceae','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 11',10,'[569]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-14 11:12:59','admin'),(2294,'Leptochromothrix','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 11',2293,'[569]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-14 11:12:42','admin'),(2295,'Leptochromothrix valpauliae','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 11',2294,'[569]','','Species',NULL,'','US 227661','BLCC-M82 = ULC 597','Marine, epipsammic or within dislodged floating mats','[113]',1,1,'',0,'active','2021-05-14 11:12:17','admin'),(2296,'Leptochromothrix engenei','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 12',2294,'[569]','','Species',NULL,'','US 227662','BLCC-M83 = ULC 598','Marine, epipsammic or within dislodged floating mats','[113]',0,1,'',0,'active','2021-05-14 11:12:11','admin'),(2297,'Ophiophycus','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 14',2293,'[569]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-14 11:12:48','admin'),(2298,'Ophiophycus aerugineus','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 14',2297,'[569]','','Species',NULL,'','US 227666','BLCC-M88 = ULC 599','Epipelic on silty marine sediments near mangroves and in floating mats near mangroves','[113]',1,1,'',0,'active','2021-05-14 11:12:22','admin'),(2299,'Vermifilum','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 14',2293,'[569]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-14 11:12:52','admin'),(2300,'Vermifilum ionodolium','Berthold, Lefler et Laughinghouse 2021. Molecular Phylogenetics and Evolution 160: 107010, p. 15',2299,'[569]','','Species',NULL,'','US 223412','BLCC-M29 = ULC 454','Epilithic on partially submerged coastal intertidal limestone, epipelic on sand or silt, and found forming benthic mats near mangroves.','[113]',1,1,'',0,'active','2021-05-14 11:12:36','admin'),(2301,'Affixifilum','Lefler, Berthold et Laughinghouse 2021. Journal of Phycology 57: 97',2413,'[571]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 13:15:25','admin'),(2302,'Affixifilum floridanum','Lefler, Berthold et Laughinghouse 2021. Journal of Phycology 57: 99',2301,'[571]','','Species',NULL,'','US 227641','BLCC-M61','Shallow subtropical marine waters','[113]',1,1,'',0,'active','2021-05-14 12:52:33','admin'),(2303,'Affixium granulosum','Lefler, Berthold et Laughinghouse 2021. Journal of Phycology 57: 100',2301,'[571]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:597',0,'active','2021-05-14 12:52:40','admin'),(2304,'Lyngbya regalis','Curren et Leong 2018. Phytotaxa 367(2): 122',1,'[572]','Holotype insufficiently specified (no herbarium or other collection is mentioned)','Species',NULL,'','','WCP1',NULL,NULL,0,0,'',1,'active','2021-05-14 12:52:15','admin'),(2305,'Neolyngbya regalis','Lefler, Berthold et Laughinghouse 2021. Notulae Algarum No. 182',595,'[571][573]','','Species',NULL,'','US 227641','BLCC-M54 = ULC586',NULL,NULL,0,1,'',0,'active','2021-05-14 13:13:50','admin'),(2306,'Neolyngbya biscayensis','Lefler, Berthold et Laughinghouse 2021. Journal of Phycology 57: 101',595,'[571]','','Species',NULL,'','US 227649','BLCC-M69 = ULC 530','Shallow subtropical marine waters','[113]',0,1,'',0,'active','2021-05-14 13:13:31','admin'),(2307,'Thermostichales','Komárek et Strunecký 2020. Fottea 20(2): 174',1,'[574]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-21 07:55:47','admin'),(2308,'Thermostichaceae','Komárek et Strunecký 2020. Fottea 20(2): 174',2307,'[574]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-21 08:04:13','admin'),(2309,'Thermostichus','Komárek et Strunecký 2020. Fottea 20(2): 174',2308,'[574]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-21 08:04:07','admin'),(2310,'Synechococcus vulcanus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-21 08:04:27','admin'),(2311,'Thermostichus vulcanus','(Copeland) Komárek et Strunecký 2020. Fottea 20(2):174',2309,'[574]','','Species',NULL,'','neotype CBFS A-092-1','',NULL,NULL,1,1,'clades:2310',0,'active','2021-05-21 08:04:04','admin'),(2312,'Synechococcu elongatus var. amphigranulatus','Copelant 1936',1,'[374]','','',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2021-05-27 12:19:47','admin'),(2313,'Synechococcus elongatus var. amphigranulatus','Copeland 1936',1,'[374]','','',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2021-05-27 12:19:26','admin'),(2314,'Synechococcus elongatus var. amphigranulatus','Copland 1936',1,'[374]','','',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2021-05-27 12:39:01','admin'),(2315,'Synechococcus arcuatus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:14:36','admin'),(2316,'Thermostichus arcuatus','(Copeland) Komárek et Strunecký 2020. Fottea 20(2):174',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2315',0,'active','2021-05-27 13:17:35','admin'),(2317,'Synechococcus bigranulatus','Skuja 1933',326,'','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:14:47','admin'),(2318,'Synechococcus elongatus var. amphigranulatus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:15:03','admin'),(2319,'Synechococcus lividus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:14:55','admin'),(2320,'Synechococcus vescus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:15:16','admin'),(2321,'Synechococcus praelongus','Emoto et Yoneda 1940',326,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2021-05-27 13:15:28','admin'),(2322,'Synechococcus sublividus','Emoto et Yoneda 1941',326,NULL,NULL,'Species',NULL,NULL,'','',NULL,NULL,0,1,NULL,0,'active','2021-05-27 13:12:56','admin'),(2323,'Synechococcus sulphuricus','Dor 1967',326,'[575]','type not specified (does not meet requirements of art. 40. 1. ICN)','Species',NULL,'','','',NULL,NULL,0,0,'',0,'active','2021-05-27 13:24:10','admin'),(2324,'Synechococcus viridissimus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-27 13:15:22','admin'),(2325,'Thermostichus bigranulatus','(Skuja) Komárek et Strunecký 2020. Fottea 20(2):174',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2317',0,'active','2021-05-27 13:30:51','admin'),(2326,'Thermostichus lividus','(Copeland) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2319',0,'active','2021-05-27 13:30:55','admin'),(2327,'Thermostichus praelongus','(Emoto et Yoneda) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2321',0,'active','2021-05-27 13:30:59','admin'),(2328,'Thermistichus sublividus','(Emoto et Yoneda) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2322',0,'active','2021-05-27 13:30:47','admin'),(2329,'Thermostichus sulphuricus','(Dor) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','invalid due to invalidity of basionym','Species',NULL,'','','',NULL,NULL,0,0,'clades:2323',0,'active','2021-05-27 13:31:03','admin'),(2330,'Thermostichus vescus','(Copeland) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2320',0,'active','2021-05-27 13:31:06','admin'),(2331,'Thermostichus viridissimus','(Copeland) Komárek et Strunecký 2020. Fottea 20(2):175',2309,'[574]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2324',0,'active','2021-05-27 13:31:08','admin'),(2332,'Parasynechococcus marenigrum','Coutinho, Tschoeke, Thompson et Thompson in Komárek et al. 2020. Fottea 20(2)182',418,'[574]','','Species',NULL,'','CBFS A–094–1','WH 8102','Marine/oceanic picoplankton from tropical to subpolar zones','',1,1,'',0,'active','2021-05-27 14:00:47','admin'),(2333,'Pseudanabaenales','',1,NULL,NULL,'Order',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-05-28 06:39:09','admin'),(2334,'Thermosynechococcaceae','Komárek, Strunecký et Johansen 2020. Fottea 20(2): 183',2530,'[574]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 11:54:54','admin'),(2335,'Synechococcus elongatus var. vestitus','Copeland 1936',326,'[374]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-05-28 06:52:59','admin'),(2336,'Thermosynechococcus vestitus','(Copeland) Komárek et Sgtrunecký 2020. Fottea 20(2): 184',330,'[574]','epitype CBFS A-120-1','Species',NULL,'','neotype Copeland 1936, p. 59, fig. 24','NES2133',NULL,NULL,1,1,'clades:2335',0,'active','2021-05-28 06:52:33','admin'),(2337,'Picosynechococcus','Komárek, Johansen et Strunecký 2020. Fottea 20(2): 185',2287,'[574]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 14:24:15','admin'),(2338,'Picosynechococcus fontinalis','Komárek, Johansen et Strunecký 2020. Fottea 20(2): 185',2337,'[574]','','Species',NULL,'','CBFS A-093-1','FG-1','freshwater bodies in the area of warm, mineral pools','[52]',1,1,'',0,'active','2021-05-28 06:58:16','admin'),(2339,'Alborzia','Nowruzi et Soares 2021. IJSEM, p. 8',16,'[576]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-06-11 06:01:39','admin'),(2340,'Alborzia kermanshahica','Nowruzi et Soares 2021. IJSEM, p. 8',2339,'[576]','','Species',NULL,'','ALBORZ CCC1399-a','CCC1399-b = MCC 4116','growing in a soil sample of a paddy field','',1,1,'',0,'active','2021-06-11 06:02:01','admin'),(2341,'Nostoc punensis','Singh 2021. Plant Sys. Evol. 302: 1392',255,'[579]','','Species',NULL,'','cryopreserved MCC 2741','MCC 2741','Singh et al.: freshwater body dwelling cyanobacteria showing the potential to grow luxuriantly in<br>the transient zone between the water and the soil','[156]',0,1,'',0,'active','2021-06-21 08:53:07','admin'),(2342,'Desmonostoc punense','Saraf et al. 2018. FEMS Microbiology Letters',710,'[578]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2341',0,'active','2021-06-21 08:55:53','admin'),(2343,'Aliinostoc soli','Saraf, Singh, Dawda, Suradkar, Behere, Kotulkar, Shaikh, Kumat, Batule et Mishra 2018. FEMS Microbiology Letters 365 (24): fny272, p. 7',593,'[578]','','Species',NULL,'','cryopreserved strain MCC 3342','ZH1(3)_PS','Saraf et al. 2018: Soil dwelling strain with the pH being measured at 7.3.','[156]',0,1,'',0,'active','2021-06-21 09:15:01','admin'),(2344,'Aliinostoc tiwarii','Saraf, Singh, Dawda, Suradkar, Behere, Kotulkar, Shaikh, Kumat, Batule &nbsp;et Mishra 2018. FEMS Microbiology Letters 365 (24): fny272, p. 6',593,'[578]','','Species',NULL,'','cryopreserved strain MCC 3346','LI_PS','fresh water with pH 7,3','[156]',0,1,'',0,'active','2021-06-21 09:13:53','admin'),(2345,'Desmonostoc magnisporum','Saraf, Singh, Dawda, Suradkar, Behere, Kotulkar, Shaikh, Kumat, Batule &nbsp;et Mishra 2018. FEMS Microbiology Letters 365 (24): fny272, p. 8',710,'[578]','','Species',NULL,'','MCC 3345','AR6_PS','Singh et al. 2018: Freshwater dwelling strain with the pH being measured at 7.3. The temperature at the time of samplingwas 32.4◦C while the electrical conductivity was 90 μS','[156]',0,1,'',0,'active','2021-06-21 09:20:54','admin'),(2346,'Pseudoaliinostoc','Lee, Ki et Lee 2021. Phytotaxa 479(1): 60',34,'[580]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-06-21 09:25:52','admin'),(2347,'Pseudoaliinostoc soli','(Saraf &amp; Singh et al.) Lee, Ki et Lee 2021. Phytotaxa 479(1): 61',2346,'[580]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:2343',0,'active','2021-06-21 09:31:09','admin'),(2348,'Pseudoaliinostoc tiwarii','(Saraf &amp; Singh et al.) Lee, Ki et Lee 2021. Phytotaxa 479(1): 61',2346,'[580]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2344',0,'active','2021-06-21 09:32:12','admin'),(2349,'Pseudoaliinostoc sejongens','Bang, Ki et Lee 2021. Phytotaxa 479(1): 62',2346,'[580]','','Species',NULL,'','NIBRCY 0000001020','FBCC-A406','Floodplain soil','[40]',0,1,'',0,'active','2021-06-21 10:24:07','admin'),(2350,'Aliinostoc catenatum','Kabirnataj et al. 2020. IJSEM 70:3420',593,'[581]','','Species',NULL,'','GCC 20201','SA24','in a garden densely mixed with grass','[244]',0,1,'',1,'active','2022-08-23 10:42:35','admin'),(2351,'Aliinostoc magnakinetifex','Kabirnataj et al. 2020. IJSEM 70:3422',593,'[581]','','Species',NULL,'','GCC 20202','SA18','soil in garden','[244]',0,1,'',0,'active','2021-06-21 10:49:11','admin'),(2352,'Aliinostoc constrictum','Kabirnataj et al. 2020. IJSEM 70:3422',593,'[581]','','Species',NULL,'','GCC 20203','SA30','field filled with stagnant water','[244]',0,1,'',0,'active','2021-06-21 10:54:06','admin'),(2353,'Desikacharya constricta','Kabirnataj et al. 2020. IJSEM 70:3424',1424,'[581]','','Species',NULL,'','GCC 20204','SA10','paddy field filled with stagnant water','[244]',0,1,'',0,'active','2021-06-21 11:02:54','admin'),(2354,'Desmonostoc persicum','Kabirnataj et al. 2020. IJSEM 70:3425',710,'[581]','','Species',NULL,'','GCC 20205','SA14','paddy field','[244]',0,1,'',0,'active','2021-06-21 11:06:51','admin'),(2355,'Pseudoaliinostoc constrictum','(Kabirnataj et al.) Lee, Ki et Lee',2346,'[580]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2352',0,'active','2021-06-21 11:10:05','admin'),(2356,'Constrictifilum','Chavadar et al. 2021. FEMS Microbiology Letters 368, fnab057, p. 9',34,'[582]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-06-28 10:53:52','admin'),(2357,'Constrictifium karadense','Chavadar et al. 2021. FEMS Microbiology Letters 368, fnab057, p. 9',2356,'[582]','','Species',NULL,'','MCC 4007','MKW3','Chavader at al. 2021: Growing as a part of cyanobacterial/algal bloom in water logged<br>sugarcane field.','[156]',1,1,'',0,'active','2021-06-28 10:58:57','admin'),(2358,'Anthocerotibacter','F.-W. Li 2021. Current Biology 31: e2',2524,'[583]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:31:47','admin'),(2359,'Anthocerotibacter panamensis','F.-W. Li 2021. Current Biology 31: e3',2358,'[583]','','Species',NULL,'','BH 283079','UTEX 3164','in hornwort <em>Leiosporoceros dussii</em>','[102]',1,1,'',0,'active','2021-06-28 11:57:32','admin'),(2360,'Amazonocrinis','Alvarenga et al. 2021. IJSEM71: 004811, p. 6',34,'[584]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-07-14 12:09:52','admin'),(2361,'Amazomocrinis nigriterrae','Alvarenga et al. 2021. IJSEM71: 004811, p. 7',2360,'[584]','','Species',NULL,'','SP428476','CENA 67','soil','[172]',1,1,'',0,'active','2021-07-16 10:39:49','admin'),(2362,'Atlanticothrix','Alvarenga et al. 2021. IJSEM71: 004811, p. 8',34,'[584]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-07-14 12:17:10','admin'),(2363,'Atlanticothrix silvestris','Alvarenga et al. 2021. IJSEM71: 004811, p. 8',2362,'[584]','','Species',NULL,'','SP428478','CENA 357','Garcinia gardneriana leaves','[172]',1,1,'',0,'active','2021-07-16 10:39:55','admin'),(2364,'Dendronalium','Alvarenga et al. 2021. IJSEM71: 004811, p. 9',34,'[584]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-07-14 12:24:20','admin'),(2365,'Dendronalium phyllosphaericum','Alvarenga et al. 2021. IJSEM71: 004811, p. 10',2364,'[584]','','Species',NULL,'','SP428479','CENA 369','Euterpe edulis leaves','[172]',1,1,'',0,'active','2021-07-16 10:40:11','admin'),(2366,'Gloeocapsopsis crepidinum','(Thuret) Geither ex Komárek 1993. Bull. Natl. Sci. Mus. Tokyo, Ser. B (Bot.), 19: 24.',191,'[585]','','Species',NULL,'','epitype HBG 024929','LEGE 06123=CCAP1425/1',NULL,NULL,1,1,'',0,'active','2021-08-05 11:01:48','admin'),(2367,'Gloeocapsopsis dulcis','Azusa-Bustos et Jung 2021. Fronties in Microbiology 12: p. 7',191,'[585]','','Species',NULL,'','HBG 024931','AAB1=DSM 112007','Hypolithic biofilm under quartz stones of the Coastal Range of the Atacama Desert.','[178]',0,1,'',0,'active','2021-08-05 11:00:58','admin'),(2368,'Gloeocapsopsis diffluens','Jung et Büdel 2021. Fronties in Microbiology 12: p. 8',191,'[585]','','Species',NULL,'','HBG 024928','PJ S16=DSM109259','Hypolithic biofilm under quartz stones','[178]',0,1,'',0,'active','2021-08-05 11:06:16','admin'),(2369,'Baaleninema','Samylina, Sinetova, Kupriyanova and Tourova 2021. FEMS Microbiology Ecology 97, fiab 104: 20',50,'[586]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-08-27 12:35:49','admin'),(2370,'Baaleninema simplex','Samylina, Sinetova, Kupriyanova and Tourova 2021. FEMS Microbiology Ecology 97, fiab 104: 21',2369,'[586]','','Species',NULL,'','cryopreserved strain PCC 7105 in stored in PCC','PCC 7105',NULL,NULL,1,1,'',0,'active','2021-11-03 16:28:41','admin'),(2371,'Sodalinema orleanskyi','Samylina, Sinetova, Kupriyanova and Tourova 2021. FEMS Microbiology Ecology 97, fiab 104: 21',1639,'[586]','','Species',NULL,'','cryopreserved strain Ey-1201','IPPAS B-2037 = Ey-1201','Biofilms in saline-alkaline lakes.','[232]',0,1,'',0,'active','2021-08-27 13:21:19','admin'),(2372,'Sodalinema gerasimenkoae','Samylina, Sinetova, Kupriyanova and Tourova 2021. FEMS Microbiology Ecology 97, fiab 104: 22',1639,'[586]','','Species',NULL,'','cryopreserved strain B-353','CCALA 1011 = IPPAS B-353','Cyanobacterial mats, biofilms and Ctenocladus communities in saline-alkaline and soda lakes.','[117]',0,1,'',0,'active','2021-08-27 13:21:12','admin'),(2373,'Sodalinema stali','Samylina, Sinetova, Kupriyanova and Tourova 2021. FEMS Microbiology Ecology 97, fiab 104: 22',1639,'[586]','','Species',NULL,'','cryopreserved strain CCY 9619','CCY 3619 = DSM 101427 = SAG 31.92 = IPPAS B-2050','Marine cyanobacterial mats.','[60]',0,1,'',0,'active','2021-08-27 13:21:06','admin'),(2374,'Dulcicalothrix alborzica','Nowruzi et Shalygin 2021. Fottea 21(2): 237',1960,'[587]','','Species',NULL,'','ALBORZ CCCC1387-a','CCC1387–b','on sumberged pebbles in river bank','[244]',0,1,'',0,'active','2021-09-15 06:55:18','admin'),(2375,'Nostoc favosum','Cai et Li 2021. Fottea 21(2): 261',255,'[588]','','Species',NULL,'','HBI JLCN201401','CHAB5709','Free–living on edge of a stream in the soil','[38]',0,1,'',0,'active','2021-09-15 07:23:28','admin'),(2376,'Nostoc mirabile','Cai et Li 2021. Fottea 21(2): 261',255,'[588]','','Species',NULL,'','HBI HBCN201402','CHAB 5784','Free–living on wet rocky substrates','[38]',0,1,'',0,'active','2021-09-15 13:36:41','admin'),(2377,'Pinocchia daecheonga','Kim, Choi, Ki et Lee 2021. Phytotaxa 510(2): 138',440,'[589]','','Species',NULL,'','NIBR CY0000001019','FBCC A230','planktonic species living in freshwater lakes in lentic and mesotrophic states','[40]',0,1,'',0,'active','2021-09-29 14:31:32','admin'),(2378,'Thermoleptolyngbya sichuanensis','Daroch, Tang, and Shah 2021. Frontiers in Microbiology 12: 696102',459,'[590]','holotype does not meet criteria of ICN (metabolically inactive)','Species',NULL,'','','A183 = FACHB-2491','thermal springs','[38]',0,0,'',0,'active','2021-10-07 13:26:02','admin'),(2379,'Thermoleptolyngbya oregonensis','Sciuto et Moro 2016. Molecular Phylogenetics and Evolution 105: 33',459,'[117]','','Species',NULL,'','PAD A000627','PCC 8501','thermal environment','[113]',0,1,'',0,'active','2021-10-07 13:23:44','admin'),(2380,'Tenebriella','Hauerová, Hauer et Kaštovský 2021. Molecular Phylogenetics and Evolution 165: 107293, p. 4',50,'[591]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-10-07 13:43:54','admin'),(2381,'Tenebriella amphibia','Hauerová, Hauer et Kaštovský 2021. Molecular Phylogenetics and Evolution 165: 107293, p. 4',2380,'[591]','','Species',NULL,'','CBFS A-123','RMCB14 = CCALA 1132','flooded sand pit','[54]',1,1,'',0,'active','2021-10-07 13:45:46','admin'),(2382,'Oscillatoria curviceps','Agardh ex Gomont 1892. Annales des Sciences Naturelles, Botanique, S´erie 7 16: 213',258,'[145]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2021-10-07 13:53:17','admin'),(2383,'Tenebriella curviceps','(Agardh ex Gomont) Hauerová, Hauer et Kaštovský 2021. Molecular Phylogenetics and Evolution 165: 107293, p. 5',2380,'[591]','','Species',NULL,'','lectotype in LD, epitype CBFS A-124','CCALA 1133',NULL,NULL,0,1,'clades:2382',0,'active','2021-10-07 13:57:08','admin'),(2384,'Euryhalinema palustris','Chakraborty et Mukherjee 2021. Phytotaxa 522(3): 182',1891,'[592]','The orthographic error in species epithet was corrected (i.e. from <em>​pallustris </em>​to <em>​palustris</em>​)​​​​ ​​​​​​','Species',NULL,'','cryopreserved strain MCC 3172','MCC 3172','soil surface','[156]',0,1,'',0,'active','2021-10-15 08:33:18','admin'),(2385,'Aerofilum','Chakraborty et Mukherjee 2021. Phytotaxa 522(3): 182',1034,'[592]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-10-15 08:36:35','admin'),(2386,'Aerofilum fasciculatum','Chakraborty et Mukherjee 2021. Phytotaxa 522(3): 182',2385,'[592]','The structures denoted as \'gas vesicles\' by the authors are not gas vesicles.','Species',NULL,'','cryopreserved strain MCC 3478','MCC 3478','Soil surface','[156]',1,1,'',0,'active','2021-10-15 08:44:43','admin'),(2387,'Waterburya','Bonthond et Shalygin 2021. Antonie van Leeuwenhoek',54,'[593]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-10-26 13:18:48','admin'),(2388,'Waterburya agarophytonicola','Bonthond et Shalygin 2021. Antonie van Leeuwenhoek',2387,'[593]','','Species',NULL,'','C A-99685','KI4T','epiphyte on Agarophyton vermiculophyllum','[60]',1,1,'',0,'active','2021-10-26 13:26:41','admin'),(2389,'Cryptochroococcus','Y. Wang, N. Jia et R. Li 2021. Journal of Phycology',16,'[594]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-11-11 12:09:33','admin'),(2390,'Cryptochroococcus tubeticus','Y. Wang, N. Jia et R. Li 2021. Journal of Phycology',2389,'[594]','','Species',NULL,'','HBI CHABTP2001','CHAB TP201716.4','Surfaces of wet rocks along the shore of Lake Cuo’e','[38]',1,1,'',0,'active','2021-11-11 12:37:22','admin'),(2391,'Limnococcus fonticola','Y. Wang, N. Jia et R. Li 2021. Journal of Phycology',228,'[594]','','Species',NULL,'','HBI CHABT2002','CHAB TP201720.1','Algal mats at the bottom of a spring in the hot spring zone of Qinghai-Tibet Plateau','[38]',0,1,'',0,'active','2021-11-11 12:45:56','admin'),(2392,'Altericista','Averina, E. Polyakova, Senatskaya &amp; Pinevich 2021. Jsournal of Phycology 57: 1526',62,'[595]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2021-11-11 13:29:18','admin'),(2393,'Altericista lacusladogae','Averina, E. Polyakova, Senatskaya &amp; Pinevich 2021. Jsournal of Phycology 57: 1526',2392,'[595]','','Species',NULL,'','LE A0000363','CALU 1127','middle latitude freshwater pools; in plankton, benthos, or periphyton','[117]',1,1,'',0,'active','2021-11-11 13:35:58','admin'),(2394,'Altericista violacea','Averina, E. Polyakova, Senatskaya &amp; Pinevich 2021. Jsournal of Phycology 57: 1526',2392,NULL,NULL,'Species',NULL,NULL,'LE A0000369','CALU 1077','middle latitude freshwater pools; in plankton, benthos, or periphyton','[117]',0,1,NULL,0,'active','2021-11-12 07:18:56','admin'),(2395,'Altericista variichlora','Averina, E. Polyakova, Senatskaya &amp; Pinevich 2021. Jsournal of Phycology 57: 1527',2392,'[595]','','Species',NULL,'','LE A0000372','CALU 1173','middle latitude freshwater pools; in plankton, benthos, or periphyton','[117]',0,1,'',0,'active','2021-11-12 07:36:55','admin'),(2396,'Aliterella vladivostokensis','Abdulin, A.Y. Nikulin, Bagmet et V.Y. Nikulin 2021. Phytotaxa 527(3): 223',466,'[596]','','Species',NULL,'','VLA CA-1212','VCA-43','aerophytic (concrete)','[117]',0,1,'',0,'active','2021-12-06 13:07:39','admin'),(2397,'Thainema','Rasouli-Dogaheh et Hauer 2022. PLoS ONE 17(1): e0261682, p. 13',61,'[597]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 10:08:19','admin'),(2398,'Thainema salinarum','Rasouli-Dogaheh et Hauer 2022. PLoS ONE 17(1): e0261682, p. 13',2397,'[597]','','Species',NULL,'','CBFS A-119-1','CCALA10287','solar saltern','[166]',1,1,'',0,'active','2022-01-14 11:02:40','admin'),(2399,'Speleotes','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 10',7,'[598]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 11:23:54','admin'),(2400,'Speleotes  anchialus','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 10',2399,'[598]','','Species',NULL,'','TAU-A01015','TAU-MAC 1118','on the surface of (immersed) rocks near artificial light, in the entrance of the anchialine cave Túnel de la Atlantida in Jameos del Aqua','[88]',1,1,'',0,'active','2022-01-14 11:35:33','admin'),(2401,'Haliplanktos','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 11',7,'[598]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 11:49:38','admin'),(2402,'Haliplanktos anthonyquinnii','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 11',2401,'[598]','','Species',NULL,'','TAU-A01016','TAU-MAC 3018','on the subsurface of rocks, close to seawater in the intertidal zone','[62]',1,1,'',0,'active','2022-01-14 11:58:00','admin'),(2403,'Olisthonema','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 11',44,'[598]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 12:03:06','admin'),(2404,'Olisthonema eestii','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 11',2403,'[598]','','Species',NULL,'','TAU-A01017','TAU-MAC 3318','freshwater, epiphytic, benthic','[56]',1,1,'',0,'active','2022-01-14 12:11:29','admin'),(2405,'Speos','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 12',61,'[598]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 12:14:17','admin'),(2406,'Speos fyssasii','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',2405,NULL,NULL,'Species',NULL,NULL,'TAU-A01018','TAU-MAC 5718','mats in terrestrial show cave near artificial light and under dropping water','[62]',1,1,NULL,0,'active','2022-01-14 12:19:46','admin'),(2407,'Stenomitos pantisii','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',481,'[598]','','Species',NULL,'','TAU-A01019','TAU-MAC 4318','epilithic mats on the surface of rocks, under low sunlight and high moisture in Grava cave','[62]',0,1,'',0,'active','2022-01-14 12:25:49','admin'),(2408,'Komarekiella chia','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',447,'[598]','','Species',NULL,'','TAU-A01020','TAU-MAC 0117','epilithic mats on the surface of calcareous substrate in a terrestrial cave, near artificial light','[62]',0,1,'',0,'active','2022-01-14 12:35:22','admin'),(2409,'Cyanocohniella hyphalmyra','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',709,'[598]','','Species',NULL,'','TAU-A01021','TAU-MAC 3117','epilithic mats on the surface of rocks in the shore of the brackish lake','[62]',0,1,'',0,'active','2022-01-14 12:42:05','admin'),(2410,'Nodularia mediterranea','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',254,'[598]','','Species',NULL,'','TAU-A01022','TAU-MAC 3317','benthos of a shallow brackish lagoon- lake','[62]',0,1,'',0,'active','2022-01-14 12:47:17','admin'),(2411,'Iphianassa','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',39,'[598]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 12:50:06','admin'),(2412,'Iphianassa zackieohae','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 166: 107322, p. 13',2411,'[598]','','Species',NULL,'','TAU-A01023','TAU-MAC 2318','brown mats in the cave wall with direct sunlight in Grava cave','',1,1,'',0,'active','2022-01-14 12:57:20','admin'),(2413,'Sirenicapillariaceae','D.E. Berthold, Lefler &amp; Laughinghouse 2022. Phycologia',10,'[599]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 13:12:08','admin'),(2414,'Sirenicapillaria','D.E. Berthold, Lefler et Laughinghouse 2022. Phycologia',2413,'[599]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 13:18:24','admin'),(2415,'Sirenicapillaria glauca','D.E. Berthold, Lefler et Laughinghouse 2022. Phycologia',2414,'[599]','','Species',NULL,'','US 227772','BLCC-M125.','Epipsammic, epiphytic and floating on marine water surface','[113]',0,1,'',0,'active','2022-01-14 13:23:54','admin'),(2416,'Sirenicapillaria rigida','D.E. Berthold, Lefler et Laughinghouse 2022. Phycologia',2414,'[599]','','Species',NULL,'','US 227691','BLCC-M116','Benthic, wrapped around seagrasses in marine coasts.','[113]',0,1,'',0,'active','2022-01-14 13:29:01','admin'),(2417,'Sirenicapillaria stauglerae','D.E. Berthold, Lefler &amp; Laughinghouse 2022. Phycologia',2414,'[599]','','Species',NULL,'','US 227770','BLCC-M121','Benthic on marine coasts.','[113]',1,1,'',0,'active','2022-01-14 13:42:26','admin'),(2418,'Tigrinifilum','D.E. Berthold, Lefler &amp; Laughinghouse 2022. Phycologia',2413,'[599]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-01-14 13:44:06','admin'),(2419,'Tigrinifilum floridanum','D.E. Berthold, Lefler &amp; Laughinghouse 2022. Phycologia',2418,'[599]','','Species',NULL,'','US 223427','BLCC-M48','Entangled within larger benthic cyanobacteria or dislodged floating mats.','[113]',1,1,'',0,'active','2022-01-14 13:48:21','admin'),(2420,'Tigrinifilum guerandense','D.E. Berthold, Lefler &amp; Laughinghouse 2022. Phycologia',2418,'[599]','','Species',NULL,'','US 227675','BLCC-M99','Entangled within cyanobacterial mats of inland salt flats.','[59]',0,1,'',0,'active','2022-01-14 13:53:21','admin'),(2421,'Capilliphycus flaviceps','Lefler, D.E. Berthold &amp; Laughinghouse 2022. Phycologia',1129,'[599]','','Species',NULL,'','US 227779','BLCC-M137','within floating marine mats of larger filamentous cyanobacteria','[113]',0,1,'',0,'active','2022-01-14 13:58:05','admin'),(2422,'Capilliphycus guerandensis','Lefler, D.E. Berthold &amp; Laughinghouse 2022. Phycologia',1129,'[599]','','Species',NULL,'','US 227655','BLCC-M76','Hypersaline pools within inland salt flats.','[59]',0,1,'',0,'active','2022-01-14 14:02:06','admin'),(2423,'Limnospira fusiformis','(Voronichin) Nowicka-Krawczyk, Mühlsteinová et Hauer 2019. Scientific Reports 9: 694, p. 6',1108,'[309]','','Species',NULL,'','','SAG 85.79 = CCALA 026 = UTEX 2340',NULL,NULL,1,1,'synonyms:761',0,'active','2022-01-20 12:47:36','admin'),(2424,'Porphyrosiphon annulatus','D. Kim, N. Lee, S. Yoon, T. Kim, Ki et O. Lee 2022. Phytotaxa 532(3): 293',277,'[600]','','Species',NULL,'','NIBR CY0000001276','FBCC-A1260','on the moist soil under the rock','[40]',0,1,'',0,'active','2022-02-08 07:28:13','admin'),(2425,'Euryhalinema epiphytica','V.L. Araújo, A.S. Schnadelbach, J.M.C. Nunes et T.A. Caires 2021. Phytotaxa 532(3):254',1891,'[601]','','Species',NULL,'','ALCB 125750 (strain preserved with 4% formaldehyde)','ALCB 125750','Marine, in protected areas of the mediolittoral zone, as epiphyte on benthic macroalgae <em>Bostrychia </em>Montagne (Rhodophyta) and associated to <em>Neolyngbya </em>sp.','[172]',0,1,'',0,'active','2022-02-08 07:46:50','admin'),(2426,'Timaviella edaphica','O.M. Vynogradova et Mikhailyuk 2022. Phytotaxa 532(3): 198',630,'[602]','combination not clearly indicated; basionym incorrectly cited (wrong page); basionym does not meet requirements of art. 39. 1 of the ICN (latine description or diagnosis)','Species',NULL,'','','DSM 112877','sea coast, biocrusts with dominance of cyanobacteria','[118]',0,0,'',0,'active','2022-02-08 09:36:26','admin'),(2427,'Timaviella dunensis','Mikhailyuk et O.M. Vynogradova 2022. Phytotaxa 532(3): 198',630,'[602]','','Species',NULL,'','KW A-32531','Us-6-3 = DSM112875','Sand dunes, biocrusts with dominance of cyanobacteria and streptophyte algae.','[60]',0,1,'',0,'active','2022-02-08 09:41:56','admin'),(2428,'Nunduva komarkovae','Gonzalez–Resendiz, Leon–Tejera et J.R. Johansen 2021. Journal of Phycology 57: 1703.',1105,'[603]','','Species',NULL,'','FCME C1088-K118.1','C1088-K118.1-M21','Epilithic on intertidal fringes (...; 0–1 m ASL); epilithic on a granitic rock, in partially exposed rock crevices','[100]',0,1,'',0,'active','2022-02-24 07:03:47','admin'),(2429,'Nunduva sanagustinensis','Gonzalez–Resendiz, Leon–Tejera et J.R. Johansen 2021. Journal of Phycology 57: 1705.',1105,'[603]','','Species',NULL,'','FCME C708-K271','C708-K271','Epilithic on supratidal fringes (... up to 5–6 m ASL); epilithic on granitic rock, both in partially sunny and exposed surfaces as well as slightly shadowed rock crevices.','',0,1,'',0,'active','2022-02-24 07:11:53','admin'),(2430,'Kyrtuthrix munecosensis','Gonzalez–Resendiz, Leon–Tejera et J.R. Johansen 2021. Journal of Phycology 57: 1707.',222,'[603]','','Species',NULL,'','FCME C1937-Ec','','Epilithic on an intertidal platform (..., up to 0–1 m ASL); epilithic in partially sunny and exposed granitic rock','[100]',0,1,'',0,'active','2022-02-24 07:16:56','admin'),(2431,'Kyrtuthrix totonaca','Gonzalez–Resendiz, Leon–Tejera et J.R. Johansen 2021. Journal of Phycology 57: 1708.',222,'[603]','','Species',NULL,'','FCME C399-Ec-M59','','Epilithic on an intertidal platform (..., up to 0–1 m ASL); epilithic in partially sunny and exposed granitic rock','[100]',0,1,'',0,'active','2022-02-24 09:04:44','admin'),(2432,'Pycnacronema caatingensis','Machado de Lima et Branco 2020. Phytotaxa 470(4):265',1248,'[604]','','Species',NULL,'','SJRP 32601','CATCC2','topsoil','[172]',0,1,'',0,'active','2022-03-03 06:13:07','admin'),(2433,'Pycnacronema edaphicum','Machado de Lima et Branco 2020. Phytotaxa 470(4):266',1248,'[604]','','Species',NULL,'','SJRP 32604','CATCA7','topsoil','[172]',0,1,'',0,'active','2022-03-03 06:18:40','admin'),(2434,'Gracilinea','Machado de Lima et Branco 2020. Phytotaxa 470(4):266',2555,'[604]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:33:51','admin'),(2435,'Gracilinea arenicola','Machado de Lima et Branco 2020. Phytotaxa 470(4):266',2434,NULL,NULL,'Species',NULL,NULL,'SJRP 32602','CATCC10','topsoil','[172]',1,1,NULL,0,'active','2022-03-03 06:28:31','admin'),(2436,'Marmoreocelis','Machado de Lima et Branco 2020. Phytotaxa 470(4):266',44,'[604]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-03 06:30:51','admin'),(2437,'Marmoreocelis xerophila','Machado de Lima et Branco 2020. Phytotaxa 470(4):269',2436,'[604]','','Species',NULL,'','SJRP 32603','CATCB5','topsoil','[172]',1,1,'',0,'active','2022-03-03 11:37:12','admin'),(2438,'Konicacronema','Machado de Lima et Branco 2020. Phytotaxa 470(4):269',2560,'[604]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:44:07','admin'),(2439,'Konicacronema caatingensis','Machado de Lima et Branco 2020. Phytotaxa 470(4):269',2438,'[604]','','Species',NULL,'','SJRP 32601','CATCB1','topsoil','[172]',1,1,'',0,'active','2022-03-03 11:42:42','admin'),(2440,'Allocoleopsis','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-03 13:36:09','admin'),(2441,'Allocoleopsis franciscana','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2440,'[605]','','Species',NULL,'','ASU C000005','PCC 7113','Terrestrial on greenhouse soils and biocrusts','[113]',1,1,'',0,'active','2022-03-04 17:17:31','admin'),(2442,'Funiculus','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-04 17:22:05','admin'),(2443,'Funiculus sociatus','(West et West) Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2442,'[605]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:2177',0,'active','2022-03-07 14:24:33','admin'),(2444,'Funiculus tenuis','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2442,'[605]','','Species',NULL,'','ASU C000003','HSN023 = UTEX ZZ1247','Terrestrial, commonly found in biological soil crusts.','[113]',1,1,'',0,'active','2022-03-07 14:29:03','admin'),(2445,'Crassifilum','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-07 14:30:42','admin'),(2446,'Crassifilum sonorensis','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2445,'[605]','','Species',NULL,'','ASU C000001','SON62 = UTEX ZZ1244','biological soil crust','[113]',1,1,'',0,'active','2022-03-08 13:50:35','admin'),(2447,'Arizonema','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-08 13:52:42','admin'),(2448,'Arizonema commune','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2447,'[605]','','Species',NULL,'','ASU C000000','HS024 = UTEX ZZ1248','biological soil crust','[113]',1,1,'',0,'active','2022-03-08 13:59:07','admin'),(2449,'Crustifilum','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-08 13:59:59','admin'),(2450,'Crustifilum hispaliculae','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2449,'[605]','','Species',NULL,'','ASU C000004','SEV30 = UTEX ZZ1245','biological soil crust','[113]',1,1,'',0,'active','2022-03-08 14:06:45','admin'),(2451,'Parifilum','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',44,'[605]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-08 14:11:53','admin'),(2452,'Parifilum solicrustae','Moreira-Fernandes, Giraldo-Silva, D. Roush et Garcia-Pichel 2021. Journal of Phycology',2451,'[605]','','Species',NULL,'','ASU C00002','SON57 = UTEX ZZ1246','biological soil crust','[113]',1,1,'',0,'active','2022-03-08 14:17:11','admin'),(2453,'Leptodesmis sichuanensis','Daroch, Tang et Shah 2022. Frontiers in Microbiology 12: 739625, p. 12',1285,'[606]','','Species',NULL,'','','PKUAC-SCTA121 = FACHB-3319','thermal springs','[38]',0,0,'',0,'active','2022-03-22 12:22:32','admin'),(2454,'Wollea salina','Chatchawan, Kozlíková, Komárek et Kaštovský 2022. Fottea 16(1): 48',344,'[609]','The holotype defined by the authors does not meet ICN rules (Art. 8.4).','Species',NULL,'','','CCALA 1091','on wet salty soils, sometimes slightly covered by shallow layer of water (in salines, 0–35 ppt)','[166]',0,0,'',0,'active','2022-03-22 13:42:20','admin'),(2455,'Neowollea salina','(Chatchawan, Kozlíková, Komárek &amp; Kaštovský) Tawong, Pongcharoen, Pongpadung et Ponza 2021. Notulae Algarum No. 214',1969,'[608]','Basionym is not valid.','Species',NULL,'','','',NULL,NULL,0,0,'clades:2454',0,'active','2022-03-22 13:44:59','admin'),(2456,'Borziella','Molinari et Guiry 2021. Notulae Algarum No. 177',66,'[607]','replaces name <em>Bacularia </em>​Borzì','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-22 13:54:58','admin'),(2457,'Borziella coerulescens','(Borzì) Molinari et Guiry 2021. Notulae Algarum No. 177',2456,'','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1423',0,'active','2022-03-22 13:54:03','admin'),(2458,'Caeruleovitis','Molinari &amp; Sánchez Ocharan 2021. Notulae Algarum No. 177',38,'[607]','replaces name <em>Cyanobotrys </em>​L. Hoffmann​​​','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-22 13:58:56','admin'),(2459,'Caeruleovitis lambinonii','(L.Hoffmann) Molinari &amp; Sánchez Ocharan 2021. Notulae Algarum No. 177',2458,'[607]','','Species',NULL,'','','',NULL,NULL,1,1,'clades:1452',0,'active','2022-03-22 14:02:21','admin'),(2460,'Borziella gracilis','(Komárek) Molinari et Guiry 2021. notulae Algarum No. 177',2456,'[607]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-03-22 14:04:06','admin'),(2461,'Borziella indurata','(Copeland) Molinari et Guiry 2021. Notulae Algarum No. 177',2456,'[607]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-03-22 14:05:18','admin'),(2462,'Borziella thermalis','(Frémy) Molinari et Guiry 2021. Notulae Algarum No. 177',2456,'[607]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-03-22 14:07:06','admin'),(2463,'Borziella vermicularis','Molinari et Guiry 2021. Notulae Algarum No. 177',2456,'[607]','based on <em>Rhabdoderma vermiculare</em> sensu Fedorov 1969 non Fott 1952','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-03-22 14:10:47','admin'),(2464,'Neocyanospira','Molinari et Guiry 2021. Notulae Algarum No. 177',25,'[610][607]','replaces <em>​Cyanospira</em>​ Florenzano et al. 1985​​​','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-03-22 14:16:38','admin'),(2465,'Neocyanospira capsulata','(Florenzano, Sili, Pelosi et Vincenzini) Molinari et Guiry 2021. Notulae Algarum No. 177',2464,'[607][610]','','Species',NULL,'','CBFS A-047','',NULL,NULL,1,1,'clades:586',0,'active','2022-03-22 14:22:04','admin'),(2466,'Neocyanospira globosa','(Hirano) Molinari et Guiry 2021. Notulae Algarum No. 177',2464,'[607]','','Species',NULL,'','','',NULL,NULL,0,1,'',0,'active','2022-03-22 14:23:25','admin'),(2467,'Petrachlorosaceae','F. Soares, Trovao et Portugal 2022. Jsournal of Phycology',13,'[611]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-04-11 12:48:19','admin'),(2468,'Petrachloros','F. Soares, Trovao et Portugal 2022. Journal of Phycology',2467,'[611]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-04-11 12:50:49','admin'),(2469,'Petrachloros mirabilis','F. Soares, Trovao et Portugal 2022. Journal of Phycology',2468,'[611]','','Species',NULL,'','COI00099798','ULC 683','attached to the limestone walls','[82]',1,1,'',0,'active','2022-04-11 12:55:26','admin'),(2470,'Oculatella lusitanica','Brito, Tamagnini, Melo et Kaštovský 2022. Journal of Phycology 34: 919',478,'[612]','','Species',NULL,'','CBFS A-125-1','LEGE 161147','Aerophytic, isolated from a clay pot','[82]',0,1,'',0,'active','2022-05-04 13:56:29','admin'),(2471,'Nodosilinea hunanesis','F. Cai et R. Li 2022. Diversity',565,'[613]','','Species',NULL,'','HBI HN201910','ZJJ01','Free-living in water','[38]',0,1,'',0,'active','2022-05-20 06:38:44','admin'),(2472,'Pseudoaliinostoc jiangxiense','F. Cai et R. Li 2022. Journal of Oceanology and Limnology',2346,'[614]','','Species',NULL,'','HBI JXGJ201701','CHAB 5870','wet soil','[38]',0,1,'',0,'active','2022-05-20 06:56:18','admin'),(2473,'Pseudoaliinostoc yunnanense','F. Cai et R. Li 2022. Journal of Oceanology and Limnology',2346,'[614]','','Species',NULL,'','HBI YNDL201601','CHAB 5871','Free-living in water','[38]',0,1,'',0,'active','2022-05-20 07:06:20','admin'),(2474,'Scytonema foetidum','Tawong, Pongcharoen et Nishimura 2022. Fottea 22(1): 80',302,'[615]','','Species',NULL,'','QBG 131045','NUACC06','Wet soil','[166]',0,1,'',0,'active','2022-06-21 12:44:00','admin'),(2475,'Roholtiella vulcanica','Gaysina, Singh, Johansen, Saraf, Pal et Allaguvatova 2022. Diversity 14: 620, p. 12',389,'[616]','Based on Art. 60.1 of the ICN the original specific epithet \'volcanica\' was corrected to \'vulcanica\'.','Species',NULL,'','BCAC 1','BCAC 516','tundra volcanic illuvial–humus soils down the east slope of Gorely volcano, pH 4.65, soil moisture 55%, soil temperature 12 C','[117]',0,1,'',0,'active','2022-08-04 07:00:28','admin'),(2476,'Cyanocystopsis','Stoyneva-Gärtner, Gärtner, Uzunov et J.-P. Descy 2022. Wulfenia 28: 62',11,'[617]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-04 07:22:36','admin'),(2477,'Cyanocystopsis kitagatae','Stoyneva-Gärtner, Gärtner, Uzunov et J.-P. Descy 2022. Wulfenia 28: 62',2476,'[617]','','Species',NULL,'','iconotype Figure 10A, B','','plankton in tropical lake','[234]',1,1,'',0,'active','2022-08-04 07:32:55','admin'),(2478,'Cyanocohniella rudolphia','P. Jung et Sommer 2022. Microorganisms 10:968, p. 9',709,'[618]','','Species',NULL,'','HBG 025346','SY-1-2-Y = DSM 113757','Biocrusts with moss in potash tailings pile surroundings','[60]',0,1,'',0,'active','2022-08-04 07:54:47','admin'),(2479,'Edaphophycus','N. Lee, D. Kim, T. Kim, J. Ki et O. Lee 2022. Phycological Research',44,'[619]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-05 08:14:58','admin'),(2480,'Edaphophycus epilithus','N. Lee, D. Kim, T. Kim, J. Ki and O. Lee',2479,'[619]','','Species',NULL,'','NIBRCY0000001290','FBCC-A203','brick wall','[40]',1,1,'',0,'active','2022-08-05 08:19:53','admin'),(2481,'Mojavia aguilerae','Baldarelli, Pietrasiak et J.R.Johansen 2022. Journal of Phycology',248,'[620]','','Species',NULL,'','NMC 109462','ATA2-1-KO23','biological soil crust','[178]',0,1,'',0,'active','2022-08-05 08:34:04','admin'),(2482,'Mojavia dolomitestris','Pietrasiak et J.R.Johansen 2022. Journal of Phycology',248,NULL,NULL,'Species',NULL,NULL,'NMC 109463','CMT-3FDIN-NPC3','biological soil crust','[113]',0,1,NULL,0,'active','2022-08-05 08:41:41','admin'),(2483,'Nostoc desertorum','Řeháková et Johansen 2007. Phycologia 46(5): 488',255,'[50]','','Species',NULL,'','BRY C-37691','CCALA 693','biological soil crust','[113]',0,1,'',0,'active','2022-08-05 08:51:12','admin'),(2484,'Cyanoplacoma','Molinari et Guiry 2021. Notulae Algarum 183: 2',19,'[621]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,1,'active','2022-08-11 09:33:46','admin'),(2485,'Cyanoplacoma adriatica','Hauck 1895. Kryptogamen-Flora von Deutschland, Österreich und der Schweiz. Zweite Auflage: 515',2487,NULL,NULL,'Species',NULL,'[1049][1051]','','',NULL,NULL,0,1,'synonyms:1049',0,'active','2022-08-11 14:15:12','admin'),(2486,'Kovacikia minuta','Li-Qin Shen, Renhui Li et Qiu 2022. Journal of Phycology 58: 426',445,'[622]','','Species',NULL,'','CCNU ZLHB201601','CCNU0001','shaded pond','[38]',0,1,'',0,'active','2022-08-11 13:19:05','admin'),(2487,'Cyanoplacoma','Schousboe ex Bornet et Thuret, 1876. Notes Algol. 1: 4.',19,'','','Genus',NULL,'[1050]',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-11 14:15:12','admin'),(2488,'Cyanoplacoma vesiculosa','Schousboe ex Bornet et Thuret 1876',2487,NULL,NULL,'Species',NULL,'[1053]','','',NULL,NULL,1,1,NULL,0,'active','2022-08-11 14:15:12','admin'),(2489,'Cyanoplacoma africana','Wille 1903. Deutsche Sudpolar-Expedition 1901-1903 8: 90',2487,NULL,NULL,'Species',NULL,'[1057]','','',NULL,NULL,0,1,'synonyms:1057',0,'active','2022-08-11 14:21:17','admin'),(2490,'Cyanoplacoma micrococca','Hansgirg 1892. Sitzungsberichte der Königl. Böhmischen Gesellschaft der Wissenschaften. Mathematisch-naturwissenschaftliche Classe 1892: 228.',2487,'','','Species',NULL,'','','',NULL,NULL,0,1,'synonyms:1057',0,'active','2022-08-11 14:21:12','admin'),(2491,'Cyanoplacoma regulare','Broady et Ingerfeld 1991. Phycologia 30(6): 548',2487,'[532]','','Species',NULL,'[1052]','CHR379746','','first-order streams where colonies are found attached to stable rock surfaces and to bryophytes','[134]',0,1,'',0,'active','2022-08-11 14:15:12','admin'),(2492,'Cyanoplacoma violacea','Setchell &amp; N.L.Gardner in Gardner 1918. University of California Publications in Botany 6: 456',2487,NULL,NULL,'Species',NULL,'[1055]','','',NULL,NULL,0,1,'synonyms:1055',0,'active','2022-08-11 14:17:37','admin'),(2493,'Cyanoplacoma willei','Gardner 1927. Memoirs of the New York Botanical Garden 7: 29',2487,'[215]','','Species',NULL,'[1054]','','',NULL,NULL,0,1,'synonyms:1054',0,'active','2022-08-11 14:16:50','admin'),(2494,'Aliinostoc alkaliphilum','Christodoulou, Economou-Amilli, Fiore et Sivonen 2022. Water 14: 2470, p. 7',593,'[623]','','Species',NULL,'','SP 400047','CENA 513','free-living, planktic in alkaline brackish waters.','[172]',0,1,'',0,'active','2022-08-14 09:08:45','admin'),(2495,'Aliinostoc catenatum','Kabirnataj et al. 2020. IJSEM 70:3420',593,'[581]','','Species',NULL,'','GCC 20201','GCC 20201',NULL,NULL,0,1,'',0,'active','2022-08-14 09:15:21','admin'),(2496,'Siamcapillus','Tawong, Pongcharoen, T. Nishimura et Saijuntha 2022. Phytotaxa 558(1): 36',1034,'[624]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-22 10:42:19','admin'),(2497,'Siamcapillus rubidus','Tawong, Pongcharoen, T. Nishimura et Saijuntha 2022. Phytotaxa 558(1): 36',2496,'[624]','','Species',NULL,'','QBG 132167','NUACC13','cyanobacterial mat covering on surface soil at the border of a small freshwater pond','[166]',1,1,'',0,'active','2022-08-22 10:52:32','admin'),(2498,'Hillbrichtia','Jasser, Panou, Sandzewicz, Gkelis et Kwiatowski 2022. Molecular Phylogenetics and Evolution 170: 107454, p. 11',50,'[625]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-22 11:49:49','admin'),(2499,'Hillbrichtia pamiria','Jasser, Panou, Sandzewicz, Gkelis et Kwiatowski 2022. Molecular Phylogenetics and Evolution 170: 107454, p. 12',2498,'[625]','','Species',NULL,'','TAU A01012','Cylx 15.1T','benthic mat (upstream) and as a freefloating mat (downstream) in a hot spring','[258]',1,1,'',0,'active','2022-08-22 11:54:54','admin'),(2500,'Amphirytos','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 170: 107454, p. 13',1034,'[625]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-22 11:59:26','admin'),(2501,'Amphirytos necridicus','Panou et Gkelis 2022. Molecular Phylogenetics and Evolution 170: 107454, p. 13',2500,'[625]','','Species',NULL,'','TAU A01013','TAU-MAC 0315','epilithic mat in a hot spring','[62]',1,1,'',0,'active','2022-08-22 12:06:59','admin'),(2502,'Thermoleptolyngbya hindakii (\'hindakiae\')','Panou, Kokociński et Gkelis 2022. Molecular Phylogenetics and Evolution 170: 107454, p. 13',459,'[625]','In the original paper was used incorrect specific name termination -iae (Art. 60.8 c of the ICN) &nbsp;','Species',NULL,'','TAU A01014','UNIE1T','compact mat in Uniejów artificial geothermal pond','[81]',0,1,'',0,'active','2022-08-23 10:59:41','admin'),(2503,'Microcoleus anatoxicus','Stancheva and Conklin 2020. Harmful Algae 93: 101767, p. 6',245,'[626]','','Species',NULL,'','UC 2085190','PTRS2','riverine benthic algal mat','[113]',0,1,'',0,'active','2022-08-23 11:34:20','admin'),(2504,'Aliterella compacta','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 14',466,'[627]','','Species',NULL,'','HBG 025115','DSM 112641','Photobiont of <em>Peltula clavata.</em>','[121]',0,1,'',0,'active','2022-08-23 12:34:53','admin'),(2505,'Aliterella gigantea','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 14',466,'[627]','','Species',NULL,'','HBG 025116','DSM 112646','Photobiont of <em>Peltula capensis.</em>','[228]',0,1,'',0,'active','2022-08-23 12:37:30','admin'),(2506,'Sinocapsa ellipsoidea','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 16',1821,'[627]','','Species',NULL,'','HBG 025117','DSM 112642','Photobiont of the saxicolous lichen <em>Peccania cerebriformis.</em>','[49]',0,1,'',0,'active','2022-08-23 12:44:12','admin'),(2507,'Pseudocyanosarcina','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 16',23,'[627]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-08-23 12:47:41','admin'),(2508,'Pseudocyanosarcina phycocyania','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 17',2507,'[627]','','Species',NULL,'','HBG 025114','DSM 112640','Photobiont of the saxicolous lichen <em>Peltula clavata.</em>','[121]',1,1,'',0,'active','2022-08-23 12:52:34','admin'),(2509,'Komarekiella globosa','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 18',447,'[627]','','Species',NULL,'','HBG 025113','DSM 112645','Photobiont of the lichen species<em> Lichinella cribellifera.</em>','[88]',0,1,'',0,'active','2022-08-24 06:05:52','admin'),(2510,'Komarekiella gloeocapsoidea','Jung, Büdel et Lakatos 2021. Frontiers in Microbiology 12: 728378, p. 19',447,'[627]','','Species',NULL,'','HBG 025111','DSM 112644','Photobiont of the saxicolous lichen <em>Gonohymenia </em>sp.','[54]',0,1,'',0,'active','2022-08-24 06:11:05','admin'),(2511,'Johanseniella','Pal et Singh 2022. FEMS Microbiology Letters 369 (1), p. 6',34,'[628]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2022-09-29 09:26:17','admin'),(2512,'Johanseniella tripurensis','Pal et Singh 2022. FEMS Microbiology Letters 369 (1), p. 6',2511,'[628]','','Species',NULL,'','GCC20225','URH-6-PS','Soil','[156]',1,1,'',0,'active','2022-09-29 09:32:35','admin'),(2513,'Leptothermofonsia','Daroch, Tang et Shah 2022. Frontiers in Microbiology 13: 765105, p. 12',61,'[629]','The description does not meet requirements of ICN nor ICNP.','Genus',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2022-09-30 13:27:04','admin'),(2514,'Leptothermofonsia sichuanensis','Daroch, Tang et Shah 2022. Frontiers in Microbiology 13: 765105, p. 12',2513,'[629]','The description does not meet requirements of ICN nor ICNP on typification.','Species',NULL,'','','E412 = FACHB 2490','thermal spring','[38]',1,0,'',0,'active','2022-09-30 13:34:20','admin'),(2515,'Raphidiopsis taverae','(Komárek et Komárková-Legnerová) Aguilera, Berrendero Gómez, Kaštovský, Echenique et Salerno 2018, Phycologia 57(2): 145',290,'[426]','','Species',NULL,'','','',NULL,NULL,0,1,'clades:1785',0,'active','2022-10-11 07:39:24','admin'),(2516,'Desikacharya kailashaharensis','Pal et Singh 2022. FEMS Microbiology Letters 369:9',1424,'[631]','','Species',NULL,'','GCC20222','KLS-BP-3A_PS','Pal et al. (2022): Sampling done during monsoon in the month of August from a field covered with grasses with close proximity to a small stream. Physiochemical readings include pH 7.8, EC 543 μS, TDS 386 ppm, and salt concentration 259 ppm','[156]',0,1,'',0,'active','2022-11-30 09:57:53','admin'),(2517,'Nunduva sanctimaloensis','Berthold, Werner et Laughinghouse 2022. Fottea 22(2): 194',1105,'[632]','','Species',NULL,'','US 227670','BLCC–M94 = ULC648','Benthic and epilithic in marine intertidal','[59]',0,1,'',0,'active','2022-11-30 10:27:40','admin'),(2518,'Fulbrightiella','N. Kumar, P. Singh et J.R. Johansen 2022. Journal of Phycology',1961,'[633]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-02 13:00:11','admin'),(2519,'Fulbrightiella bharadwajae','N. Kumar, P. Singh et J.R. Johansen 2022. Journal of Phycology',2518,'[633]','','Species',NULL,'','GCC20211','18G-PS','in a small vernal pool associated with a wet meadow surrounded by evergreen coniferous forests; The temperature of the water body was 12.7°C, pH 5.25, electrical conductivity 54.0 uS  m1, total dissolved solids 38.5 ppm, and salinity 27.3.','[156]',1,1,'',0,'active','2023-01-02 13:11:11','admin'),(2520,'Fulbrightiella oahuensis','J.R. Johansen et P. Singh 2022. Journal of Phycology',2518,'[633]','','Species',NULL,'','BISH 786238','HA4248- MV3','Blackish-brown mat growing on a wet rock wall','[265]',0,1,'',0,'active','2023-01-02 13:17:09','admin'),(2521,'Sherwoodiella','J.R. Johansen et P. Singh 2022. Journal of Phycology',1961,'[633]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-02 13:18:57','admin'),(2522,'Sherwoodiella mauiensis','J.R. Johansen et P. Singh 2022. Journal of Phycology',2521,'[633]','','Species',NULL,'','BISH 786239','HA4860-CV1','Epilithic in a small stream','[265]',1,1,'',0,'active','2023-01-02 13:26:43','admin'),(2523,'Aulosira bohemensis','Lukešová, J.R. Johansen, Martin et Casamatta 2009. Phycologia 48(2): 121',110,'[634]','','Species',NULL,'','BRY 37704','ISB-2 = UTEX2947','soil in wet meadow','[54]',0,1,'',0,'active','2023-01-06 14:08:54','admin'),(2524,'Anthocerobacteraceae','Strunecký et Mareš 2023',8,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:32:07','admin'),(2525,'Aegococcales','Strunecký et Mareš 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:33:13','admin'),(2526,'Aegeococcaceae','Strunecký et Mareš 2023',2525,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:34:14','admin'),(2527,'Thalassosporaceae','Strunecký et Mareš 2023',2333,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:36:39','admin'),(2528,'Gloeomargaritales','Moreira et al. 2017',1,'[81]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:38:24','admin'),(2529,'Gloeomargaritaceae','Moreira et al. 2017',2528,'[81]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-27 09:39:13','admin'),(2530,'Acaryochloridales','Strunecký et Mareš 2023',1,'[635]','invalid nominate genus','Order',NULL,'',NULL,NULL,NULL,NULL,0,0,NULL,0,'active','2023-01-31 08:30:42','admin'),(2531,'Prochlorotrichales','Strunecký et Mareš 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 11:55:58','admin'),(2532,'Prochlorotrichaceae','Burger-Wiersma et al. 1989',2531,'','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 11:57:29','admin'),(2533,'Cephalothrix alaskensis','Strunecký, Raabová, Bernardová, Ivanova, Smanova, Crossley et Kaftan 2020. FEMS Microbiology Ecology 96(3): fiz189, p. 13',1089,'[636]','','Species',NULL,'','CBFS A–108–1','L30','periphyton on the water soil shoreline','[113]',0,1,'',0,'active','2023-01-30 12:12:21','admin'),(2534,'Albertania alaskaensis','Strunecký, Raabová, Bernardová, Ivanova, Smanova, Crossley et Kaftan 2020. FEMS Microbiology Ecology 96(3): fiz189, p. 14',1030,'[636]','','Species',NULL,'','CBFS A–109–1','KL12','periphyton on willow roots','[113]',0,1,'',0,'active','2023-01-30 12:15:56','admin'),(2535,'Tildeniella alaskaensis','Strunecký, Raabová, Bernardová, Ivanova, Semanova, Crossley et Kaftan 2020. FEMS Microbiology Ecology 96(3): fiz189, p. 14',1051,'[636]','','Species',NULL,'','CBFS A–116–1','KL16','periphyton on willow roots','[113]',0,1,'',0,'active','2023-01-30 12:34:16','admin'),(2536,'Leptodesmis alaskaensis','Strunecký et Raabová 2020. FEMS Microbiology Ecology 96(3): fiz189, p. 16',1285,'[636]','Genus is not valid.','Species',NULL,'','CBFS A–111–1','V20','mat in dry channels','[113]',0,0,'',0,'active','2023-01-30 12:40:30','admin'),(2537,'Pseudophormidium americanum','Strunecký et Raabová 2020. FEMS Microbiology Ecology 93(3): fiz189, p. 15',285,'[636]','','Species',NULL,'','MK861904','KT1','Dry soil','[113]',0,1,'',0,'active','2023-01-30 13:19:13','admin'),(2538,'Gibliniella','Strunecký et Raabová 2020. FEMS Microbiology Ecology 96(3):fiz189, p. 16',416,'[636]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 13:21:46','admin'),(2539,'Gibliniella alaskaensis','Strunecký et Raabová 2020. FEMS Microbiology Ecology 96(3):fiz189, p. 16',2538,'[636]','','Species',NULL,'','CBFS A–114–1','L31','crust on stones in a lake','[113]',1,1,'',0,'active','2023-01-30 13:28:23','admin'),(2540,'Shackletoniella','Strunecký et Raabová 2020. FEMS Microbiology Ecology 96(3): fiz189, p. 16',1034,'[636]','','Genus',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-30 15:21:40','admin'),(2541,'Shackletoniella antarctica','(West et G.S.West) Strunecký, Raabová et Bernardová 2020.',2540,'[636]','','Species',NULL,'','','ULC037',NULL,NULL,1,1,'clades:1315',0,'active','2023-01-30 15:25:48','admin'),(2542,'Aliinostoc vietnamicum','Maltseva, Kezlya et Maltsev 2022. Journal of Phycology 58: 791',593,'[637]','','Species',NULL,'','MELIT HVP225','VP225','Forest soil in the monsoon tropical region with summer rains','',0,1,'',0,'active','2023-01-31 07:24:45','admin'),(2543,'Nodosilineales','Strunecký et Mareš 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:32:06','admin'),(2544,'Nodosilineaceae','Strunecký et Mareš 2023',2543,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:33:06','admin'),(2545,'Cymatolegaceae','Strunecký et Mareš 2023',2543,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 07:35:30','admin'),(2546,'Persinemataceae','Strunecký et Mareš 2023',2543,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:12:44','admin'),(2547,'Oculatellales','Strunecký et Mareš 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:14:44','admin'),(2548,'Leptolyngbyales','Strunecký et al. 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:28:43','admin'),(2549,'Neosynechococcaceae','Strunecký et Mareš 2023',2548,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 08:37:09','admin'),(2550,'Geitlerinematales','Strunecký et al. 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:19:28','admin'),(2551,'Geitlerinemataceae','Strunecký et al. 2023',2550,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:20:27','admin'),(2552,'Desertifilales','Strunecký et al. 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:22:11','admin'),(2553,'Aerosakkonemataceae','Strunecký et al. 2023',10,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:27:40','admin'),(2554,'Coleofasciculales','Strunecký et al. 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:29:52','admin'),(2555,'Wilmottiaceae','Strunecký et al. 2023',2554,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 10:31:11','admin'),(2556,'Lusitaniellaceae','Strunecký et Mareš 2023',12,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-01-31 13:24:06','admin'),(2557,'Pleurocapsaceae','GGeitler 1925',6,NULL,NULL,'Family',NULL,NULL,NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:27:21','admin'),(2558,'Halothecaceae','Strunecký et Mareš 2023',6,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:32:34','admin'),(2559,'Gomontiellales','Strunecký et Mareš 2023',1,'[635]','','Order',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 09:43:26','admin'),(2560,'Konicacronemataceae','Strunecký et Mareš 2023',2559,'[635]','','Family',NULL,'',NULL,NULL,NULL,NULL,0,1,NULL,0,'active','2023-02-01 13:43:44','admin');
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Islands',0),(23,'Jamaica','Caribbean Islands',0),(24,'Martinique','Caribbean Islands',0),(25,'Montserrat','Caribbean Islands',0),(26,'Puerto Rico','Caribbean Islands',0),(27,'Saint Bathélemy','Caribbean Islands',0),(28,'Saint Kitts and Nevis','Caribbean Islands',0),(29,'Saint Lucia','Caribbean Islands',0),(30,'Saint Martin','Caribbean Islands',0),(31,'Saint Vincent and the Grenadines','Caribbean Islands',0),(32,'Sint Maarten','Caribbean Islands',0),(33,'Trinidad and Tobago','Caribbean Islands',0),(34,'Turks and Caicos Islands','Caribbean Islands',0),(35,'Virgin Islands','Caribbean Islands',0),(36,'(Unspecified in East Asia)','East Asia',0),(37,'Hong Kong','East Asia',0),(38,'China','East Asia',0),(39,'Japan','East Asia',0),(40,'Korea','East Asia',0),(41,'Korea DPR','East Asia',0),(42,'Macao','East Asia',0),(43,'Mongolia','East Asia',0),(44,'Taiwan','East Asia',0),(45,'(Unspecified European)','Europe',0),(46,'Åland Islands','Europe',0),(47,'Albania','Europe',0),(48,'Andorra','Europe',0),(49,'Austria','Europe',0),(50,'Belgium','Europe',0),(51,'Bosnia and Herzegovina','Europe',0),(52,'Bulgaria','Europe',0),(53,'Croatia','Europe',0),(54,'Czech Republic','Europe',0),(55,'Denmark','Europe',0),(56,'Estonia','Europe',0),(57,'Faroe Islands','Europe',0),(58,'Finland','Europe',0),(59,'France','Europe',0),(60,'Germany','Europe',0),(61,'Gibraltar','Europe',0),(62,'Greece','Europe',0),(63,'Greenland','Europe',0),(64,'Guernsey','Europe',0),(65,'Hungary','Europe',0),(66,'Iceland','Europe',0),(67,'Ireland','Europe',0),(68,'Isle of Man','Europe',0),(69,'Italy','Europe',0),(70,'Jersey','Europe',0),(71,'Latvia','Europe',0),(72,'Liechtenstein','Europe',0),(73,'Lithuania','Europe',0),(74,'Luxembourg','Europe',0),(75,'Macedonia','Europe',0),(76,'Malta','Europe',0),(77,'Monaco','Europe',0),(78,'Montenegro','Europe',0),(79,'Netherlands','Europe',0),(80,'Norway','Europe',0),(81,'Poland','Europe',0),(82,'Portugal','Europe',0),(83,'Romania','Europe',0),(84,'San Marino','Europe',0),(85,'Serbia','Europe',0),(86,'Slovakia','Europe',0),(87,'Slovenia','Europe',0),(88,'Spain','Europe',0),(89,'Svalbard and Jan Mayen','Europe',0),(90,'Sweden','Europe',0),(91,'Switzerland','Europe',0),(92,'United Kingdom','Europe',0),(93,'Vatican','Europe',0),(94,'(Unspecified Mesoamerican)','Mesoamerica',0),(95,'Belize','Mesoamerica',0),(96,'Costa Rica','Mesoamerica',0),(97,'El Salvador','Mesoamerica',0),(98,'Guatemala','Mesoamerica',0),(99,'Honduras','Mesoamerica',0),(100,'Mexico','Mesoamerica',0),(101,'Nicaragua','Mesoamerica',0),(102,'Panama','Mesoamerica',0),(103,'(Unspecified in North Africa)','North Africa',0),(104,'Algeria','North Africa',0),(105,'Egypt','North Africa',0),(106,'Libya','North Africa',0),(107,'Morocco','North Africa',0),(108,'Tunisia','North Africa',0),(109,'Western Sahara','North Africa',0),(110,'(Unspecified in North America)','North America',0),(111,'Canada','North America',0),(112,'Saint Pierre and Miquelon','North America',0),(113,'United States','North America',0),(114,'(Unspecified in North Asia)','North Asia',0),(115,'Belarus','North Asia',0),(116,'Moldova','North Asia',0),(117,'Russian Federation','North Asia',0),(118,'Ukraine','Europe,North Asia',0),(119,'(Unspecified in Oceania)','Oceania',0),(120,'American Samoa','Oceania',0),(121,'Australia','Oceania',0),(122,'Clipperton Island','Oceania',0),(123,'Cocos (Keeling) Islands','Oceania',0),(124,'Cook Islands','Oceania',0),(125,'Fiji','Oceania',0),(126,'French Polynesia','Oceania',0),(127,'Guam','Oceania',0),(128,'Christmas Island','Oceania',0),(129,'Kiribati','Oceania',0),(130,'Marshall Islands','Oceania',0),(131,'Micronesia','Oceania',0),(132,'Nauru','Oceania',0),(133,'New Caledonia','Oceania',0),(134,'New Zealand','Oceania',0),(135,'Niue','Oceania',0),(136,'Norfolk Island','Oceania',0),(137,'Northern Mariana Islands','Oceania',0),(138,'Palau','Oceania',0),(139,'Papua New Guinea','Oceania',0),(140,'Pitcairn','Oceania',0),(141,'Samoa','Oceania',0),(142,'Solomon Islands','Oceania',0),(143,'Tokelau','Oceania',0),(144,'Tonga','Oceania',0),(145,'Tuvalu','Oceania',0),(146,'United States Minor Outlying Islands','Oceania',0),(147,'Vanuatu','Oceania',0),(148,'Wallis and Futuna','Oceania',0),(149,'(Unspecified in South & South East Asia)','South & South East Asia',0),(150,'Bangladesh','South & South East Asia',0),(151,'Bhutan','South & South East Asia',0),(152,'British Indian Ocean Territory','South & South East Asia',0),(153,'Brunei Darussalam','South & South East Asia',0),(154,'Cambodia','South & South East Asia',0),(155,'Disputed Territory','South & South East Asia',0),(156,'India','South & South East Asia',0),(157,'Indonesia','South & South East Asia',0),(158,'Laos','South & South East Asia',0),(159,'Malaysia','South & South East Asia',0),(160,'Maldives','South & South East Asia',0),(161,'Myanmar','South & South East Asia',0),(162,'Nepal','South & South East Asia',0),(163,'Philippines','South & South East Asia',0),(164,'Singapore','South & South East Asia',0),(165,'Sri Lanka','South & South East Asia',0),(166,'Thailand','South & South East Asia',0),(167,'Timor-Leste','South & South East Asia',0),(168,'Viet Nam','South & South East Asia',0),(169,'(Unspecified in South America)','South America',0),(170,'Argentina','South America',0),(171,'Bolivia','South America',0),(172,'Brazil','South America',0),(173,'Colombia','South America',0),(174,'Ecuador','South America',0),(175,'Falkland Islands','South America',0),(176,'French Guiana','South America',0),(177,'Guyana','South America',0),(178,'Chile','South America',0),(179,'Paraguay','South America',0),(180,'Peru','South America',0),(181,'Suriname','South America',0),(182,'Uruguay','South America',0),(183,'Venezuela','South America',0),(184,'(Unspecified in Sub-Saharan Africa)','Sub-Saharan Africa',0),(185,'Angola','Sub-Saharan Africa',0),(186,'Benin','Sub-Saharan Africa',0),(187,'Botswana','Sub-Saharan Africa',0),(188,'Burkina Faso','Sub-Saharan Africa',0),(189,'Burundi','Sub-Saharan Africa',0),(190,'Cameroon','Sub-Saharan Africa',0),(191,'Cape Verde','Sub-Saharan Africa',0),(192,'Central African Republic','Sub-Saharan Africa',0),(193,'Comoros','Sub-Saharan Africa',0),(194,'Congo','Sub-Saharan Africa',0),(195,'Congo DR','Sub-Saharan Africa',0),(196,'Côte d\'Ivoire','Sub-Saharan Africa',0),(197,'Djibouti','Sub-Saharan Africa',0),(198,'Equatorial Guinea','Sub-Saharan Africa',0),(199,'Eritrea','Sub-Saharan Africa',0),(200,'Ethiopia','Sub-Saharan Africa',0),(201,'Gabon','Sub-Saharan Africa',0),(202,'Gambia','Sub-Saharan Africa',0),(203,'Ghana','Sub-Saharan Africa',0),(204,'Guinea','Sub-Saharan Africa',0),(205,'Guinea-Bissau','Sub-Saharan Africa',0),(206,'Chad','Sub-Saharan Africa',0),(207,'Kenya','Sub-Saharan Africa',0),(208,'Lesotho','Sub-Saharan Africa',0),(209,'Liberia','Sub-Saharan Africa',0),(210,'Madagascar','Sub-Saharan Africa',0),(211,'Malawi','Sub-Saharan Africa',0),(212,'Mali','Sub-Saharan Africa',0),(213,'Mauritania','Sub-Saharan Africa',0),(214,'Mauritius','Sub-Saharan Africa',0),(215,'Mayotte','Sub-Saharan Africa',0),(216,'Mozambique','Sub-Saharan Africa',0),(217,'Namibia','Sub-Saharan Africa',0),(218,'Niger','Sub-Saharan Africa',0),(219,'Nigeria','Sub-Saharan Africa',0),(220,'Réunion','Sub-Saharan Africa',0),(221,'Rwanda','Sub-Saharan Africa',0),(222,'Saint Helena, Ascension and Tristan da Cunha ','Sub-Saharan Africa',0),(223,'Sao Tomé and Principe','Sub-Saharan Africa',0),(224,'Senegal','Sub-Saharan Africa',0),(225,'Seychelles','Sub-Saharan Africa',0),(226,'Sierra Leone','Sub-Saharan Africa',0),(227,'Somalia','Sub-Saharan Africa',0),(228,'South Africa','Sub-Saharan Africa',0),(229,'South Sudan','Sub-Saharan Africa',0),(230,'Sudan','Sub-Saharan Africa',0),(231,'Swaziland','Sub-Saharan Africa',0),(232,'Tanzania','Sub-Saharan Africa',0),(233,'Togo','Sub-Saharan Africa',0),(234,'Uganda','Sub-Saharan Africa',0),(235,'Zambia','Sub-Saharan Africa',0),(236,'Zimbabwe','Sub-Saharan Africa',0),(237,'(Unspecified in West & Central Asia)','West & Central Asia',0),(238,'Afghanistan','West & Central Asia',0),(239,'Armenia','West & Central Asia',0),(240,'Azerbaijan','West & Central Asia',0),(241,'Bahrain','West & Central Asia',0),(242,'Cyprus','West & Central Asia',0),(243,'Georgia','West & Central Asia',0),(244,'Iran','West & Central Asia',0),(245,'Iraq','West & Central Asia',0),(246,'Israel','West & Central Asia',0),(247,'Jordan','West & Central Asia',0),(248,'Kazakhstan','West & Central Asia',0),(249,'Kuwait','West & Central Asia',0),(250,'Kyrgyzstan','West & Central Asia',0),(251,'Lebanon','West & Central Asia',0),(252,'Oman','West & Central Asia',0),(253,'Pakistan','West & Central Asia',0),(254,'Palestine, State of','West & Central Asia',0),(255,'Qatar','West & Central Asia',0),(256,'Saudi Arabia','West & Central Asia',0),(257,'Syrian Arab Republic','West & Central Asia',0),(258,'Tajikistan','West & Central Asia',0),(259,'Turkey','West & Central Asia',0),(260,'Turkmenistan','West & Central Asia',0),(261,'United Arab Emirates','West & Central Asia',0),(262,'Uzbekistan','West & Central Asia',0),(263,'Yemen','West & Central Asia',0),(264,'(Any country)','Cosmopolitan',0),(265,'Hawaii (USA)','Oceania',0);
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INSERT INTO `cyanodb_data` VALUES (1,102,'diagnosis','Trichomata aequalia vel ad apices sensim attenuata, evaginata vel vaginis saepius evanescentibus cincta, libera vel in stratum mucosum congesta. Cellulae apicales difformes. Heterocystae intercalares plures. Sporae situs varii, modo heterocystis utrinque contiguae, modo inter cellulas vegetativas ortae, solitariae vel catenatae. (Conf. Wittrock in Wittrock et Nordstedt, Algae exsicc., n° 496.)','Bornet et Flahault (1888)',NULL,0,0),(2,104,'diagnosis','Thallus minimus squamiformis, aerugineus, libere natans, e filis in laminulas plumosas vel in fasciculos fusiformes aggregatis formatus; trichomata evaginata, utrinque attenuata; sporae cylindricae elongatae in inlervallo heterocystarum formatae, solitariae, inter heterocystas sparsae.','Bornet et Flahault (1888)',NULL,0,1),(3,228,'diagnosis','Genus cyanocaryoticum, cum cellulis in coloniis parvis consociates, non filamentosum. Coloniae mucilaginosae, paecipue microscopicae, natantes, lobatae vel abbitu irregulari, (1)2-ad 40 cellullares, cum cellulis praecipae distantis, irregualriter ordinatis, vel 2-4-8 indistincte aggregatae. Mucus coloniae tenuis, sine colore, homogeneus, interdum ad marginnem diffluens. Cellulae sphaericae, post divisionem hemisphaericae, aeruginosae, griseo-virides, olivaceo-virides vel lutescentes, ad 22 lm in diametro. Divisio cellularum in planos duas vel tres in generationes subsequentibus, cellulae filiales in forma<br>sphaerica ante divisionem sequentem crescent.','Komárková et al. (2010)',NULL,0,0),(4,108,'diagnosis','Trichomala cylindracea, evaginata, in spiram eximie regularem plus minusve laxam contorta, apice aequalia aut attenuata; cellula apicalis superne rotundata; calyptra nulla.','Gomont (1892)',NULL,0,0),(5,110,'diagnosis','Fila libera aequalia, sparsa, vel in fasciculos approximata, vaginata. Vaginae membranaceae arctae. Trichomata indefi- nita ex articulis aeque longis ac latis, cylindricis vel doliiformibus, ultimis conformibus rotundatis. Heterocystae intercalares. Sporae in intervallo inter heterocystas ortae, ab eis remotae vel juxta eas positae, cylindricae, catenatae.','Bornet et Flahault (1888)',NULL,0,0),(6,114,'diagnosis','Trichomata evaginata, libera, ambitu oblonga, paucirticulata.','Gomont (1892)',NULL,0,0),(7,116,'diagnosis','Frons initio solida, demum cava, filis nostochineis, in gelatina nidulantibus farcta. Fila flexuoso-curvata, parallela, sursum attenuata et in apicem piliformem desinentia, ramosissima. Pseudo-rami nunc Scytonematum modo gemini li- beri,nunc sursum simplices basi cruribus duobus divergentibus suffulti. Vaginae in junioribus distinctae, tubulosae, demum confluentes obsoletae. Heterocystae intercalares sine ullo ordine positae.','Bornet et Flahault (1887)',NULL,0,0),(8,118,'diagnosis','Cyanobacterium filamentosum, ad substrata praecipue subaerophytica adherens, strata tomentosa formans; filamenta cum vaginis firmis, plus minusve dense irregulariterque fasciculata, isopolares, cylindrica, cum heterocytis solitariis intercalaribus; ramificatio tolypotrichoideum vel scytonematoideum rarissime praesens. Akinetae carentes. Reproductio hormogoniis, apice filamentis liberantibus. Typus generis <i>Brasilonema bromeliae</i>, spec. nova.','Fiore et al. (2003)',NULL,0,0),(9,140,'diagnosis','[diagnosis of <i>Erythrosphaera</i>]: <i>Erythrosphaera marina</i> gen. nov., sp. nov. is a unicellular cyanobacterium that has been observed in and cultured from surface water of the tropical Atlantic from 15°N to 30°S (off the coast of Brazil) when the water temperature exceeded 26°C. It has coccoid cells, 2-5 µm in diameter, that divide in two successive planes at right angles to one another. This cyanobacterium contains phycoerythrin, very rich in phycourobilin, as its major light harvesting pigment; is an obligate photoautotroph and will only grow in a restricted range between 26°-34°C. In continuous illumination <i>E. marina</i> grew in a simple mineral medium with nitrate or ammonia as sources of combined nitrogen, but did not fix dinitrogen under these conditions when combined nitrogen was absent. However, when incubated in a diel light/dark cycle (14 hr L/10 hr D, in 25 µEin m<sup>-2</sup>sec<sup>-1</sup> at 27°C in a mineral medium devoid of combined nitrogen, <i>E. marina</i> fixed dinitrogen and grew with a 35 hr doubling time. Experiments have shown that <i>E. marina</i> photosynthesizes and accumulates glycogen during the light period and then uses the stored glycogen reserves to drive nitrogen fixation at night. The details of this diel separation of photosynthesis and dinitrogen fixation will be discussed and compared with the strategies used by other nitrogen-fixing cyanobacteria. [invalid diagnosis]<strong> </strong>','Waterbury et al. (1988 : 1089)',NULL,0,0),(10,137,'diagnosis','Fila subdichotome divisa. Trichomata Saepe pluria (2-oo ) in vagina communi inclusa. Heterocystae basilares. Sporae (secundum Borzi) majores, ovatae vel ellipticae, singulae aut pauciseriatae, interjectae, exosporio crassiusculo. Caespites penicillati. Plantae aquae dulcis.','Bornet et Flahault (1888)',NULL,0,0),(11,142,'diagnosis','Trichomata libere natantia, brevia vel longa, recta vel circinata, cylindrica, leve constricta vel non-constricta ad septa, ad 6 um lata, ad apices clare acuta. Cellulae cylindraceae, protoplasmate subtiliter granulari et aerotopis facultative impletis; cellulae apicales<br> elongatae, attenuatae et acuminatae, plerumque hyalinae. Heterocytae inter-calares, solitariae, cylindraceae ad ellipticae. Akinetes intercalares, solitariae vel rare bi-nae, elongatae, ab heterocytis remotae vel confines. - Planktice in aquis.<strong> </strong>','Rajaniemi et al. (2005)',NULL,0,0),(12,141,'diagnosis','Fila cyanoprocaryotica, isopolaria, uniseriata, simplicia, solilaria vel in aggregationibus liberis plus minusve irregulariter disposita, sine vaginis conspicuis, curta, recta, arcuata vel paulo flexuosa. Trichomata paucicellularia (ad 35-cellularia), usque ad 120 um longa, cylindrica, cum helerocylis sporisque, ad dissepimenta constricta. Cellulae vegetativae sphaericae, doliiformes, ovales ad cylindricae. Heterocytae binatim in parte centrali trichomatis, per divisionem symmetricam unae cellulae vegetativae oriundae; trichomata postea inter heterocytis intercalaribus separantur; heterocytae sphaerieae vel ovales, in trichomatibus adultis in positione terminali. Akineta solitaria vel in seriebus, ovalia vel cylindrica, apo- vel paraheterocytice evolventia.<br> <br>','Komárek et al. (2010)',NULL,0,0),(13,149,'diagnosis','Coloniae microscopicae, liberae, gelatinosae aut indefinitae. Cellulae solitariae liberae, in muco irregulariter dispersae, elongatae, contentu, aerugineo, homogeneo, cum pseudovacuolis (aerotopis). Reproductio divisione cellularum perpendiculariter ad axem transver salem in duas partes, et disintegratione coloniarum.','Hindák (2002)',NULL,0,1),(14,148,'diagnosis','Coloniae libere natantes. Cellulae solitariae, geminatae vel 4 in serie brevi intra mucum colonialem irregulariter distributae. Cellulae solitariae calyptra brunnea ambitu semicirculari in extremo unico (verosimiliter praecipitia ferrea). Geminatae vel seriales calyptra unica vel calyptris in extremis ambobus. Cellulae minutissimae sine aerotopis. Divisio cellularis fissione binaria simplici divisio nis plano unico. Cellula filialis una tantum calyptra statim post divisionem, postea calyptra nova ad cellulae filiali alterae extremum oppositum formata est. Cellulae post divisionem saepe in positione obliqua vel etiam parallela rotatant.','Joosten (2006)',NULL,0,1),(15,166,'diagnosis','Trichomata aequalia, brevia, evaginata, muco amorpho involuta, in stratum indefinite expansum aggregata; articuli cylindrici diamelro longiores. Heterocystae terminales. Sporae sub heterocysta ortae, singulae, rarius plurimae seriatae. (Conf. Thuret, Observations sur la reproduction de quelques Nostochinees, in Memories de la Soc. des sc. de Cherbourg, 1857, t. V; - Borzi, Morfologia, etc., in Nuovo Giornale bot. ital., 1878, vol. X.)','Bornet et Flahault (1888)',NULL,0,0),(16,165,'diagnosis','Trichomata recta vel spiraliter connexa, leviter contracta versus fines; cellulae cylindricales cum nullis vel haud ullis constrictionibus ad parietes transversas; heterocystae semper terminales; cum trichomata fragmentur, novae heterocystae orientur adterminos liberos trichomatum per transformationem cellularum vegetativarum terminalium ; sporae praesentes intercalares in situ.<br>','Seenayya et Subba Raju (1972)',NULL,0,0),(17,171,'diagnosis','Fila subdichotome divisa; trichomata saepe pluria (2-6) in vagina communi inclusa. Heterocystae nunc basilares , nunc intercalares, in unica specie nullae. Caespites penicillati vel pulvinati.','Bornet et Flahault (1886)',NULL,0,0),(18,183,'diagnosis','Thallus filiformis ramosus e filis numerosis intra vaginam communem fasciculatim inclusis formatus. Fila pscudoramosa dense congesta. Heterocystae terminales et intercalares. Planta marin Symplocae hydnoidis faciem haud male referens.','Bornet et Flahault (1886)',NULL,0,0),(19,187,'diagnosis','Cellulae cyanoprocaryoticae, solitariae, sphaericae vel paucim ovales, post divisionem hemisphaericae et mox binae (quattuor) coniunctae, nunquam in coloniis, 3-10 um in diametro, sine mucilagine, vel cum involucris tenuis, diffluentibus, incoloris, circum cellulis solitariis. Cellulae aeruginosae, griseo-virides vel subroseae. Contentu cellularum homogeneo, sine separatio in centro- et chromatoplasma, interdum, cum stiis longitudinalibus (positio thylakoidarum). Systema thylokoidarum in cellulis longitudine plus minusve paralleliter vel irregulariter ordinata. Divisio cellularum in partes duas similares in planos duas in generationes subsequentis; cellulae filiales, aequales, hemisphaericae, crescentes in status originali subgloboso ante proxima divisione. Cellulae semper in cellulis duobus filialis dividuntur in planes perpendiculares in generaciones subseqventes.','Korelusová et al. (2009)',NULL,0,1),(20,193,'diagnosis','Frons sphaerica nunc usque ad extremum solida, nunc aetate progrediente inflato-cava. Fila e centro radiantia, pseudo-ramosa. Vaginae ad basim trichomalum perspicuae, superne in gelatinam amorpham confluentes. Trichomata flagelliformia, interrupte torulosa. Heterocystae basilares. Sporae e cellula heterocystam superante formatae, in basi vaginae persistentis et earum tegumentum exterius constituentis involutre. Hormogonia seriata numerosa.','Bornet et Flahault (1887)',NULL,0,0),(21,199,'diagnosis','Fila libera, lateraliter haud concreta, e cellulis singulis, rarius binis formata, ramosa. Rami erecti a filo primario re- pente parum diversi. Vaginae fere ubique continuae. Heterocystae intercalares. Plantae aquaticae, caespitoso-floccosae, tenerae. (Conf. Itzigsohn, Skizzen zu einer Lebensgeschichte des Hapalosiphon Braunii, 1855; - Borzi, Morfologia etc., in N. Giornale bot. ital., XI, p. 381,1879.)','Bornet et Flahault (1888)',NULL,0,0),(22,200,'diagnosis','Fila fragilia pseudo-ramosa; pseudo-rami solitarii, eruptione laterali trichomatis formati, sub heterocysta ipsa, rarius inter heterocystas, egredientes. Vagina tenuis, sicca, fragilis. Algae crustaceo-tomentosae, minutae.','Bornet et Flahault (1888)',NULL,0,1),(23,205,'diagnosis','Thallus crustiformis vel caespitosus, purpureus vel violaceus, e duobus stratis formatus : inferiore horizontaliter ex- panso, intricato, filamentoso, vel e cellulis minutis in lineas radiatas subseriatis contexto; superiore verticali, filis erectis simplicibus, hinc illinc in pilum mox evanescentem attenuatis constante. Vaginae tenues, arctissimae, continuae. Hormogonia solitaria vel seriata. Sporae...<strong> </strong>Bornet et Flahault (1886) sub <i>Leptochaete</i> Borzi: Fila simplicia, saepius tenerrima, thallum indefinite crustiformem, tenuem, plerumque late effusum efficientia. Multiplicatio hormogoniis et conidiis chroococcoideis ex articulorum basalium<br> transmutatione ortis.','Kirchner: Bornet et Flahault (1886) sub <i>Amphithrix</i> Kützing',NULL,0,0),(24,208,'diagnosis','Thallus e filis longitudinaliter concretis formatus, nunc in stratum expansus, nunc filiformis erectus, laciniato-ramosus, membrana communi nulla circumdatus. Vaginae membranacea tenues, saepe muco involutae et confluentes, hyalinae. Trichomata moniliformia. Heterocystae intercalares. Sporae nondum visae.','Bornet et Flahault (1888)',NULL,0,0),(25,211,'diagnosis','Fila plus minusve pseudo-ramosa pulvinulos caespitosos rarissime calce induratos, aut caespites jndefinitos, etiam strata haud caespitosa<br> phormidioidea formantia. Vaginae semper hyalinae, cylindraceae, sublamellosae, plus minusve mucosae vel subamorphae et aetate provecta omnino diffluentes, chlorozincico iodurato nunquam caerulescentes. Trichomata intra vaginam pauca, saepius laxe aggregata; articuli diametro trichomatis breviores, in speciebus nonnullis brevissimi; apex trichomatis rectus, plus minusve altenuatus, capitatus membrana cellulae apicalis superne in calyptram incrassata.<br>','Gomont (1892)',NULL,0,0),(26,212,'diagnosis','Frondes irregulariter et vage divisae; fila saepius plura in vagina communi inclusa. Heterocystae intercalares. Bornet et Flahault (1888) sub <i>Hormothamnion</i>: Thallus e filis longitudinaliter concretis formatus, nunc in stratum expansus, nunc filiformis erectus, laciniato-ramosus, membrana communi nulla circumdatus. Vaginae membranacea tenues, saepe muco involutae et confluentes, hyalinae. Trichomata moniliformia. Heterocystae intercalares. Sporae nondum visae.','Bornet et Flahault (1888)',NULL,0,1),(27,215,'diagnosis','Thallus planus, crustaceus, orbicularis, tennis, pagina inferiori adnatus, ambitu crescens. Fila parallela erecta sim- plicia, rarius parce pseudoramosa. Heterocystae basilares. Sporae ignotae. Plantae marinae.<br>','Bornet et Flahault (1886)',NULL,0,0),(28,216,'diagnosis','Thallus parvus aut minimus, laete caeruleus vel dilute aerugineo-olivascens, submembranaceo-lubricus. Trichomata tenerrima (4-5 ?m crassa) recta, apices versus sensim attenuata, paralleliter decurrentia, fasciculatim et densissime congregata, articulis elliptico aut sphaerico-compressis, arcte et saepe oblique connexis, plerumque mutua pressione angulosis. Sporae exacte globosae, cellulis vegetativis duplo majores, aureo-fuscae, exosporio crasso, subtiliter granulato-scabro.','Bornet et Flahault (1888)',NULL,0,0),(29,223,'diagnosis','Plantae epiphyticae, marinae. Fila medio affixa, utrinque erecta. Vaginae tenues, hyalinae.','Gomont (1892) sub subgenus',NULL,0,0),(30,234,'diagnosis','Fila vaginata, libera, simplicia, nunc caespitosa, nunc in stratum floccosum vel pannosum intricata. Vaginae firmae, tenues aut, aetate provecta, crassae et lamellosae, hyalinae, rarius luteo-fuscae. Trichomata in speciebus nonnullis ad genicula constricta, apice recta, aequalia aut leviter attenuata; membrana cellulae apicalis nonnunquam in calyptram incrassata.','Gomont (1892)',NULL,0,0),(31,241,'diagnosis','Fila libera, irregulariter ramosa. Articuli, praeter ramigeros, unica cellula constantes. Rami biformes, partim cylin- drici, partim flagelliformes (in pilum attenuati). Vagina continua. Heterocystae singulae (rarissime binae) terminales vel laterales, numquam intercalares. Multiplicatio hormogoniis [et cellulis chroococcoideis?]. Sporae ignotae. Contentus cellularum homogeneus.','Bornet &amp; Flahault (1888)',NULL,0,0),(32,248,'diagnosis','Genus cyanoprocaryoticum generis <i>Nostoc </i>similis. Coloniae microscopicae in natura, subsphaericae, ellipsoideae vel irregulares, tegumentis firmis et mucilaginosis circumdatae, despues in seriebus macroscopicis, repentis vel erectis ordinatae in vitro; series subcoloniis pseudofilamentosae, de subcoloniis et microcoloniis compositae, praecipue in vitro. Cellulae subsphaericae, in coloniis in trichomas uniseriatas vel pluriseriatas et valde flexuosas conjunctae, ad dissepimenta valde constrictae, vel in aggregationis densis agglomeratae. Heterocytae semper terminales, vel laterales in agglomerationis, heterocytae intercalares raris. Coloniae iuvenes cum heterocytis utrinque terminalibus. Reproductio disintegratione coloniis, cellulis solitariis liberantis de coloniis, vel hormogoniis<br> paulocellularibus. Hormogoniae germinantes sine heterocytis, saepe cum cellulis binis dilatatis intercalaribus; hormogoniae plerumque acute flexae inter cellulis dilatatis.','Řeháková et al. (2007)',NULL,0,1),(33,245,'diagnosis','Fila simplicia aut vage pseudo-ramosa, ad terram repentia, necnon inter varias Algas vigentia. Vaginae hyalinae plus minusve regulariter cylindraceae, haud lamellosae, in speciebus pluribus demum diffluentes, in unica specie chlorozincico ioduralo caerulescentes. Trichomata in filis bene evolutis intra vaginam permulta, arcte congesta, saepe funiformi- contorta; apex trichomatis rectus, attenuatus; cellula apicalis acute, rarius obtuse conica, in<br> unica specie capitata.','Gomont (1892)',NULL,0,0),(34,244,'diagnosis','Fila simplicia, basi affixa, erecta. Trichomata in vagina solitaria. Heterocystae basilares<br> et intercalares. Sporae (ubi cognitae) e cellulis inferioribus formatae. Plantae minutae, marinae vel aquae dulcis, in caespitibus stellatis vel tomentosis aggregatae.','Bornet et Flahault (1888)',NULL,0,0),(35,254,'diagnosis','Fila libera vaginata. Trichomata sterilia eximie aequalia. Vagina hyalina arcta, plerumque tenerrima, mucosa, nonnun- quam evanescens. Articuli breves depressi, disciformes. Heterocystae compressae. Sporae globosae, subglobosae vel disciformes, in intervallo heterocystarum seriatae, episporio laevi. (Voyez Bornet et Thuret, Notes algologiques, pl. XXIX.).','Bornet et Flahault (1888)',NULL,0,0),(36,255,'diagnosis','Thallus mucosus, gelatinosus vel coriaceus, initio globosus vel oblongus, demum in speciebus diversis formas varias induens (globosus, foliosus, filiformis, bullosus, maculiformis), solidus vel cavus, liber vel affixus, strato corticali densiori (peridermide dicto) et saturatius colorato cinctus. Fila flexuoso-curvata et implicata, in thallum coalita; vaginae nunc ubique distinctae, nunc confluentes indiscernendae. Trichomata saepius torulosa. Articuli sphaerico-depressi, dolii formes vel cylindrici. Heterocystae intercalares et (in junioribus) terminales. Sporae sphaericae vel oblongae, ad medium inter heterocystas seriatae, evolutione centrifuga (Conf. Borzi, Morfologia, etc., in Nuovo Giornale bot. ital., 1878, vol. X, p. 241).','Bornet &amp; Flahault (1888)',NULL,0,0),(37,256,'diagnosis','Frons gelatinosa, defnita. Trichomata unica serie cellularum formata, ramosa. Heterocystae intercalares et laterales, pedicellatae vel sessiles. Planta aquatica, Rivulariis cavis subsimilis.','Bornet et Flahault (1886)',NULL,0,0),(38,258,'diagnosis','Trichomata cylindracea, libera, evaginata, aut rarius vaginis pertenuibus, fragilibus, mucosis inclusa, interdum ad genicula constricta, haud moniliformia, pice saepius attenuata recta curvata vel plus minusve regulariter terebriformia, in speciebus nonnullis vulgo, sed non constanter, per totam longitudiem spiralia; membrana cellulae apicalis in speciebus pluribus superne incrassata.','Gomont (1892)',NULL,0,0),(39,267,'diagnosis','Fila vaginata, simplicia, in stratum pannosum adhaerens aut rarius fluitans basi affixum et laciniatum agglomerata, haud sine ruptura segreganda. Vaginae tenues, hyalinae, mucosae, agglutinantes, pro parte aut omnino diffluentes. Trichomata cylindracea, in speciebus nonnullis ad genicula constricta, etiam moniliformia, apice saepius attenuato recta aut curvata, capitata aut non capitata, nunquam evidenter spiralia; membrana cellulae apicalis in speciebus<br> pluribus superne in calyptram incrassata.','Gomont (1892)',NULL,0,0),(40,269,'diagnosis','Cellulae in colonias aggregatae, raro solitariae vel binae. Coloniae microscopicae, libere natantes, cum cellulis solitaris, sine tegumentis gelatinosis communibus. Cellulae cyanoprocaryoticae, sine aerotopis (pseudovacuolis), muco hyalino tectae. Mucus cellulae bilamelosus. Divisio cellularum in partes duas. Reproductio desintegratione coloniarum.','Hindák (2002)',NULL,0,0),(41,266,'diagnosis','Cyanophycea filamentosa; filamenta solitaria vel in colonias aggregata, praecipue periphytica, e trichomatibus vaginisque composita, heteropolaria, raro false divaricata. Vaginae plus minusve firmae, praecipue lamellosae, interdum coloratae, ad apices apertae, trichomam<br> unam continentes. Trichomata heteropolaria, basim dilatata (1.5-13.2 um lata), ad apices gradatim et flagellatim attenuata at elongata, semper sine heterocytis, akinetis et aerotopis. Cellulae contentu homogeneo vel granuloso, perpendiculariter dividuntur, ad apices elongatae, contentu plus minusve hyalino; cellula apicalis tenuis cylindrica,<br> elongata. Reproductio desintegratione trichomatum.<strong> </strong>','Anagnostidis (2001)',NULL,0,0),(42,273,'diagnosis','Fila vaginata, libera, eruptione laterali trichomatis pseudo-ramosa, pseudo-ramis solitariis aut geminatis. Vaginae firmae, hyalinae, rarius luteo-aureae. Trichomata frequenter ad genicula constricta; apex trichomatis rectus, rarissime attenuatus; calyptra nulla. <br> Plantae <i>Scytonematis</i> facie, saepius caespitosae et hydrophilae.<br>','Gomont (1892)',NULL,0,0),(43,277,'diagnosis','Fila simplicia. Vaginae purpurae aut persicinae. Trichomata intra vaginam solitaria; cellula apicalis haud capitata.','Gomont (1892)',NULL,0,0),(44,296,'diagnosis','Thallus hemisphaericus, globosus vel inflato-lobatus cavus, interdum in stratum indefinitum confluens. Fila e centro radiantia, repetite pseudo-ramosa. Heterocystae basilares. Sporae nondum notae.','Bornet et Flahault (1886)',NULL,0,0),(45,291,'diagnosis','A generis totis in Microchaetaceis divisione cellularum in planis duobus differt. Fila pseudoramosa, trichomis solitariis vel paucis. Trichomae isopolares. Hormogonia paucicellulares, divisibilia in plana duo.','Casamatta et al. (2006)',NULL,0,0),(46,297,'diagnosis','Trichomata solitaria, evaginata, brevissima 1—8 (16) cell., saepissime 4 cell., arcuata aut spiraliter contorta, anfractibus 1—2 (plerumque incompletis), ad genicula constricta. Cellulae cylindricae; diametro longiores, (0,8—1,5 u crass., 3,5—9 u long), apicibus rotundatis aut applanatis. Cytoplasma homogeneum, hyalinum, luteo-viride aut pallide-aeruginosum, dissepimenta partim uno granulo notata. crass. cell. 1,3—1,5 u long. cell. 4-9 u.','Koczwara (1929: 108) [diagnosis of <em>Raciborskia</em>]',NULL,0,0),(47,299,'diagnosis','Trichomata irregulariter caespitoso-aggregata, 2 — plura vagína commuii fuscescente, lamelloso stratificata, valde ampliato-saccata, demum apice soluta, involuta et thallum exiguum gelatinosum laciniato-lobulatum constituentia; pseudoramulis brevibus, moniliformibus, discretis, heterocysta basilari, globosa instructis; sporis aureo-fuscis, articulos vegetativos duplo superantibus; exosporio crassiusculo scabro.<strong> </strong>','Bornet &amp; Flahault (1886)',NULL,0,0),(48,300,'diagnosis','Fila pulvinulos definitos, saepe calce induralos, aut fasciculos<br> erectos, prostratos vel fluctuantes formantia, aut in stratum pannosum intricata, saepe inferne trunciformia, superne crebre, rarius parce pseudo-ramosa et subsimplicia. Vaginae hyalinae, luteo-fuscae vel purpureae, passim caeruleae, firmae, lamellosae, apice acuminatae, chlorozincico iodurato in speciebus fere cunctis caerulescentes. Trichomata intra vaginam pauca, plus minusve laxe aggregata; articuli diametro trichomatis saepius longiores, nunquam eo multo breviores; apex trichomatis rectus, plerumque attenuatus, haud capitatus. Membrana cellulae apicalis superne non incrassata. Plantae terrestres vel aquaticae, nunquam omnino marinae, frequenter in stillicidiis vigentes.<br>','Gomont (1892)',NULL,0,1),(49,302,'diagnosis','Fila pseudo-ramosa; pseudo-rami solitarii vel gemini ex eruptione laterali trichomatis formati, in intervallo heterocystarum, interdum quoque, sed rarius, sub ipsis heterocystis egredientes. Trichomata in vagina solitaria, recta. Hormogonia terminalia solitaria. Sporae, in paucis speciebus tantum visae, sphaericae aut ovatae, exosporio tenui et laevi. (Conf. Borzi, loc. cit., 1879, p. 368.) <br> <strong>Diagnosis of Diplocolon </strong>Nägeli: Bornet et Flahault (1887): Fila pseudo-ramosa; pseudo-rami solitarii vel gemini ex eruptione laterali trichomatis formati, in intervallum hetero- cystarum, interdum quoque, sed rarius, sub heterocystis ipsi egredientes. Trichomata in vagina communi pluria, contorta Thallus difformis, constrictus, irregulariter claviformis. Terrestris.','Bornet &amp; Flahault (1886)',NULL,0,0),(50,308,'diagnosis','Fila elongata caespitosa, fruticulosa, subdichotome ramosa. Vaginae firmae aut vix diffluentes, haud coloratae, cy- lindraceae, non lamellosae,\r\nchlorozincico iodurato non caerulescentes. Trichomata intra vaginam numerosa, in fasciculos plures distinctos saepe aggregata; apex trichomatis rectus; cellula apicalis conica, haud capitata.','Gomont (1892)',NULL,0,0),(51,313,'diagnosis','Coloniae microscopicae, natantes, cavae, sphaericae vel rare juvenes irregulares, postea sphaerae cavae aut irregulares, complanatae, prominentiis ornatae vel prominentiis nullis, saepe clathratae, cellulae in strato unico dispositis superficiem coloniae versus; involucrum mucilaginosum inconspicuum, incolor; cellulae sphaericae distantes dispositae; contentus cellularis aerotopis munitus. Cellulae divisio in planis duobus perpendicularibus ad coloniae superficiem. Multiplicatio coloniarum fragmentatione.','Azevedo et Sant\'Anna (2003)',NULL,0,0),(52,315,'diagnosis','Colonia molliter acervata in agaro, marginibus leviter irregularibus, non caespitosa, atroveneta, remantes atroveneta ad menses quatuor; olivacea vel ochracea ad mortem cellulosum in culturis vetustioribus siccis. Colonia compacta, filis dense dispositis, non mucilagina. Fila non horizontaliter vel verticaliter extensa e colonia etsi visibiles intra coloniam. Morphologia colonialis similaris in ambobus agaro basali Boldii et agaro Z-8. Fila spiras arctas regulares formantia, 6-20 um diametro. Spirae leviter decrescentes in culturis novis, 16-28 um diametro ad partem latissimam, 12-16 um diametro ad extrema angustata spirarum, distantia inter spiras regulares 8-12(-16) um. Fila interdum in spiras laxiores contorta vel etiam extensa, haec in culturis vetustioribus frequentiora. Rami falsi duplices vel simplices, in spiras laxas vel in fila extensa praesentes, non observati in spiras arctas. Rami falsi plerumque ab heterocyteis distantes. Vagina firma plerumque incolorata, interdum succinea vel umbrina, in culturis novis tenuis, in culturis vetustioribus crassiorescens, 1-4 um lata. Trichomata ad septa haud constrictae ad leviter constrictas, in culturis vetustioribus et in filis laxiter spiralibus vel extensis frequenticus constrictae, 5.5-14.0 um diametro. Cellulae plerumque breviores quam longae, infrequenter quadratae, 2.0-7.2 um longae, sine aerotopis, contentis interdum granularibus praecipue in culturis vetustioribus. Heterocyteae intra filas intercalares vel baseless, pro parte maxima simplices, in positione intercalari infrequenter duplices, raro triplices, sphaericae ad ovales, interdum in positione basali adpressae in latere uno, brunnescentes, 8-9 um diametro, 4-9 um longae.<br> Typus SRS70 die 19. Maji 1995 a solo deserti, lat. bor. 39°06.066&#39;, long. occ. 110°44.713&#39;, Pro-spectus Cunei, Sanctus Raphael Unda, Utah, USA. Holotypus hic designatus: BRY C 35162, Herbarium Cryptogamorum Nonvascularium, Brigham Young University, Provo, Utah. Isotypi: BRY C 35162, Herbarium Cryptogamorum Nonvascularium, Brigham Young University, Provo, Utah. Isotypus in statu vivo: 2660, UTEX Congeries Culturamm, University of Texas.Austin, Texas.<br> A Scytonema et Tolypothrix filis regulatim arcte torsivis in helices dextrales differt. Fila libra, regulatim arcte torsiva. Rami falsi duplices vel simplices. Vaginae firmae, tenues vel crassae, interdum lamellatae. Trichomata solitaria intra vaginam. Cellulae breviores quam latae. Heterocyteae intercalares vel basilares, sphaericae ad ovales vel adpressae. Akineta non observata.<br>','Flechtner et al.(2002)',NULL,0,0),(53,316,'diagnosis','Trichomata exilia, in spiram plus minusve laxam aut plane densam contorta, apice constanter aequalia. Protoplasma homogeneum aut vix granulosum.','Gomont(1892)',NULL,0,1),(54,321,'diagnosis','Fila libera, rarius lateraliter aggregata, in frondem definitam non concreta. Articuli filorum majorum e cellulis binis vel pluribus formati. Heterocystae saepius laterales, passim intercalares. Plantae terrestres, rigidae, atro-fuscae, vel aqua- ticae, pulvinatae, molliores. (Conf. Borzi, Morfologia e biologia delle Alghe ficocromacee, in N. Giorn. bot. ital., 1879, vol. XI, p.374.)','Bornet et Flahault (1888)',NULL,0,0),(55,324,'diagnosis','Fila vaginata, e basi prostrata ascendentia et in fasciculos erectos aut rarius plus minusve procumbentes necnon anas- tomosantes dense coalita, passim pseudoramosa, pseudoramis solitariis. Vaginae leones, hyalinae, firmae aut submucosae. Trichomata apice recta, hand raro paulum attenuata; membrana cellulae apicalis superne in speciebus nonnullis leviter incrassata.','Gomont, 1892',NULL,0,0),(56,328,'diagnosis','Thallus crustiformis vel caespitosus, purpureus vel violaceus, e duobus stratis formatus : inferiore horizontaliter ex- panso, intricato, filamentoso, vel e cellulis minutis in lineas radiatas subseriatis contexto; superiore verticali, filis erectis simplicibus, hinc illinc in pilum mox evanescentem attenuatis constante. Vaginae tenues, arctissimae, continuae. Hormogonia solitaria vel seriata. Sporae...<strong> </strong>Bornet et Flahault (1886) sub <i>Leptochaete</i> Borzi: Fila simplicia, saepius tenerrima, thallum indefinite crustiformem, tenuem, plerumque late effusum efficientia. Multiplicatio hormogoniis et conidiis chroococcoideis ex articulorum basalium<br> transmutatione ortis.','Bornet et Flahault (1886) sub <i>Amphithrix</i> Kützing',NULL,0,0),(57,330,'diagnosis','Diagnosis missing','not published',NULL,0,1),(58,333,'diagnosis','Filamenta solitaria, praecipue metaphytica vel subaerophytica, raro in coloniis planis aggregata, haud vel rarissime divaricata, cum trichomatibus sparsis vel numerosis. Vaginae plus minusve cylindricae vel (raro) ad apices attenuatae, non striatae vel tenuissime striatae, imitatae vel mucilaginosae, diffluentes, sine colore, a trichomatibus distantes. Trichomata 0.5-3 um lata. Cellulae semper longiores quam latae, cylindricae, contentu plus minusve homogeneo. Cellula apicalis conica, apiculata vel rotundata, sine calyptra.<strong> </strong>','Anagnostidis (2001)',NULL,0,0),(59,334,'diagnosis','Trichomata cylindracea, evaginata, in fasciculos squamuliformes, discretos, libere natantes muco fugacissimo aggre- gata, apice recta attenuata<br> leviter capitata. Cellula apicalis truncato-conica, calyptram convexam praebens.','Gomont (1892)',NULL,0,0),(60,332,'diagnosis','Fila pseudo-ramosa; pseudo-rami solitarii eruptione laterali trichomatis formati, sub heterocysta ipsa, interdum, sed rarius, ad medium inter heterocystas egredientes. Caespites pulvinati vel floccosi. Plantae aquae dulcis. Sporae (ubi cognitae) sphaericae, ovatae vel ellipticae, absque ordine interjectae, saepe multiseriatae, exosporio laevi et tenui (secundum Borzi:).','Bornet et Flahault (1888)',NULL,0,0),(61,343,'diagnosis','Filamenta cylindrica, plus minusve recta vel paucim flexuousa, arcuata et circinata, non ramosa, solitaria vel ad multis consociata, plus minusve paralleliter in fasciculis repentes, in muco diffluenti t sine colore, aggregata; fila singularia cum vaginis facultativis, tenuis, firmis, apice apertis, non ramosis, hyalinis, incoloratis, non lamellosis. Trichoma recta el leviter curva et flexuosa, cylindrica, ad septa non vel paucim constricta, ad apices non attenuata, 3.0-6.0 µm lata; heterocytis vel akinetis carentibus. Cellulae<br> cylindricae, aeruginosae, saepe cum granulis sparsis ed distinctis, dispersis impletae; granula interdum ad septa transversalia agglomerata; cellulae plus minusve quadraticae vel paucim brevior vel longior uam latae; cellula apicalis cylindrica, cum cellulis vegetativis similis, terminaliter obtusa, rotundata<br> vel oblonge-conica, sine calyptra. Thylakoides asciculatae, praecipue parietales vel plus minusve paralleliter vel paucim irregulariter dispositae. Cellulae perpendiculariter dividuntur, zonis meristematicis bsentibus. Reproductio disintegratione trichomatibus in partes immobilibus, necridis carentibus.','Struneský et al. (2011)',NULL,0,0),(62,344,'diagnosis','Thallus tubulosus, cylindricus, mollis. Fila subrecta paralleliter agglutinata vel leniter curvato-implicata, vaginis confluentibus. Heterocystae intercalares. Sporae catenatae heterocystis contiguae vel ab eis remotae. (Conf. Wolle, Fresh-water Algae of the United-States, p. 290, tab. 199, fig. 1.)','Bornet et Flahault (1888)',NULL,0,0),(63,196,'diagnosis','Moderately halophilic and halotolerant, benthic, marine, filamentous, non-heterocystous cyanobacteria of very thin trichomes. Growth is optimal at salinities between 4.5 and 12% (w/v) total salts and ceases above 17% and below 3%. Trichomes are cylindrical, around or slightly less than 1 |jm wide. Thylakoids are arranged concentrically and parallel to the plasma membrane, single or stacked. Pores are distributed irregularly on cell wall and septa. No junctional pores observed.','Abed et al. (2002)',NULL,0,0),(64,196,'etymology','<i>Halomicronema</i> Ha.lo.mi.cro.ne&#39;ma. Gr.n. hals, halos salt; Gr. adj. mikros, small Gr. n. n. nema, filament; M.L.n.n. Halomicronema salt-tolerant small filament','Abed et al. (2002)',NULL,0,0),(65,279,'diagnosis','Prochloraceae: Prochloron: unicellulares, capsulatae aut sine capsula mucilaginosa visibili. Unicellulares, sphaericae, sine capsula mucilaginosa visibili. Usque adhuc unus solum repro-ductionis modus cognitus, id est, divisio in duas partes per constrictionem aequatorialem. Usque adhuc inventae solum ut cellulae in coloniis ascidiarum conviventes in oris maritimis.','Lewin (1977)',NULL,0,0),(66,279,'etymology','Pro.chlo&#39;ron. Gr. prefix pro primitive; Gr. adj. chloros green; M.L. neut. n. Prochloron primitive green (cell).<strong> </strong>','Lewin (1977)',NULL,0,0),(67,236,'diagnosis','genus cyanobacteriis heterocytosis. filamenta solitaria, libere natantia vel in strata irregularia, macroscopica aggregata, sine vaginis, vel cum muco incolore, tenue, amorpho circumdatae. trichomata uniseriata, plus minusve recta vel irregulariter flexuosa, not ramosa, symmetrica vel subsymmetrica, ad dissepimenta constricta, ad apices paucim attenuata vel cylindrica, cum heterocytis duobus subapicalis, raro cum heterocyta tertia centrali. cellulae cylindricae vel paucim barriliformes, plus minusve isodiametricae vel longior quam latae, contentu aerugineo, homogeneo, cum granulis sparsis et aerotopis solitariis facultativis; cellula terminalis cylindrica vel conica, apice rotundata. heterocytae intercalares, solitariae, cylindricae, plerumque latior quam cellulae vegetativae, in trichomatibus subapicaliter dispositae, rare plus una heterocyta centralis. akinetes late ovales, intercalares, cum heterocytis conjunctae, valde ad eos partes externis dispositae, solitariae, rarissime binae, cum episporio laevi vel ornati, praecipue duas in una trichoma. reproductio trichomatibus fragmentatione et akinetis germinatione.','Komárek (2008)',NULL,0,0),(68,131,'etymology','The root ˝cystis˝ (from Greek ˝kystis˝ - bladder or bag) was incorporated into generic name of isolate 5.2 s.c.l. ... In accordance with this observation, the root ˝Chroo˝ (from Greek Chroo - skin) was incorporated into the generic name of isolate 5.2 s.c.l. ... Thus, the Greek root ˝Gloe˝ (sticky) was incorporated into the generic name of this isolate - ˝Chroogloeocystis˝.','Brown et al. (2005)',NULL,0,0),(69,141,'etymology','The genus is named to the honour of Swedish phycologist Gertrud Cronberg.','undefined',NULL,0,0),(70,271,'etymology','<i>Planktothricoides </i>(Plank.to.thric.oi´des. N.L. n. <i>Planktothrix </i>a genus of cyanobacteria; Gr. comp. oides resembling; N.L. fem. n. <i>Planktothricoides </i>resembling <i>Planktothrix </i>Anagnostidis et Komárek).','Suda et al. (2002)',NULL,0,0),(71,280,'etymology','Pro´ chlor, o.thrix. Gr. pref. protos first (primordial); Gr. adj. chloros green; Gr. n. thrix hair or thread; M.L. fern. n. Prochlorothrix primordial green hair.<strong> </strong>','Castenholz (2001)',NULL,0,0),(72,278,'etymology','Pro.chlo´ o.coc´ cus. Gr. prefix pro primitive; Gr. adj. chloros green; Gr. n. kokkos grain or kernel; M.L. masc. n. Prochlorococcus primitive green kernel (cell).','Castenholz (2001)',NULL,0,1),(73,291,'etymology','This genus is named in honor of Rex Lowe on the occasion of his 60th birthday, in appreciation of his professional accomplishments and personal friendship.&nbsp;','Casamatta et al. (2006)',NULL,0,0),(74,298,'etymology','<i>Rubidibacter</i> (Ru.bi.di.bac´ter. L. adj. <i>rubidus </i>red, reddish; N.L. masc. n. <i>bacter </i>rod; N.L. masc. n. <i>Rubidibacter </i>redcoloured rod).','Choi et al. (2008)',NULL,0,0),(75,326,'etymology','Der Name leitet sich [from Greek] von zusammenhängen und ˝Kern˝ ab.','Geitler (1942)',NULL,0,0),(76,327,'etymology','Der Name leitet sich [from Greek] von ˝zusammenhängen˝ und ˝Blase, im Sinn von kugeliger Zelle˝ ab. Er ist, wie Sauvageau selbst betont, unzutreffend, da die Zellen typischerweise nicht zusammenhängen, wurde aber gewählt, um die Ähnlichkeit mit Synechococcus hervorzuheben.','Geitler (1942)',NULL,0,0),(77,99,'description','Thallic, small clusters of free filaments; all filaments of the same morphology, flexuous, irregularly and freely tangled, laterally branched, cylindrical, composed from simple trichomes and sheaths; Sheaths thick, firm, homogeneous or layered (nothing is known about colouration). Trichomes uniserial, cylindrical, composed from moniliform rows of cells, with deep constrictions at cross walls, with a terminal growth; branches of the same width and morphology as the main filaments and trichomes; types of the true branching: T-type, pseudodichotomous V-type. Cells barrel-shaped up to cylindrical, narrowed at both ends, usually longer than wide, blue-green with a granular content and sometimes with prominent solitary granules; apical cells more cylindrical, end cells rounded. Known chroococcal stages (?, two-celled groups). Heterocytes and akinetes not known.','komárek (1992)',NULL,0,0),(78,100,'description','Unicellular - colonial; elongated cells are arranged serially into rows and pseudofilamentous colonies, and oriented by their longer axis parallely to the long axis of a colony, but shifted a little aside one to another; colonies are simple or pseudo- dichotomously branched. Sheaths (envelopes) around the rows of cells are wide, colourless, structureless, sometimes slightly diffluent at the margin. Cells rod-like, more or less rectangular with cut ends, usually a little distant one from another, with<br> pale blue-green (or greyish) content.','komárek (1992)',NULL,0,0),(79,98,'description','Thallic, branched filaments; thallus irregular, flattened, endolithic, composed from free, irregularly disposed, tangled, branched filaments. Filaments unsheathed, but with wide, fine, colourless, difluent, sametime slightly visible, rarely brownish and limited mucilaginous envelopes. Trichomes uniserial, irregularly waved , more o less cylindrical or with slightly irregularly swollen cells, at the ends sametimes slightly widened, not constricted or constricted at cross walls; types of the true branching: T- type, pseudodichotomous V- type, reverse Y- type; trichomes sometimes irregularly barrelshaped, isodiametric or longer than wide, end cell rounded; cell content blue- green, homogeneous. Heterocytes and akinetes not known.','komárek (1992)',NULL,0,0),(80,101,'description','Filamentous; filaments isopolar, long, solitary or in groups, cylindrical, in the middle usually arcuated or irregularly curved, with firm sheaths, which are sometimes yellowish brown coloured and layered; sometimes occur false branchings. Trichomes at cross walls slightly constricted or unconstricted, uniserial, attenuated at both ends and sometimes terminated by long, thin hairs with co1ourless cells. Heterocytes and akinetes always missing.','komárek (1992)',NULL,0,0),(81,102,'description','Filamentous; filaments solitary or in free clusters (subg. Dolichospermum) or in macroscopic mats on the substrate (subg. Anabaena), usually with coiled and tangled, sometimes up to screw-like coiled, rarely with more or less parallel oriented trichomes, along the length of the same width or slightly narrowed to the ends, with more or less deep constrictions at cross walls, always without firm sheaths, but sometimes with mucilaginous, hyaline, colourless, often diffluent envelopes; trichomes uniserial, often moniliform, isopolar, always metameric (heterocytes develop solitary and intercalary in more or less certain distances one from another; in one developed trichome always 3-9, rarely more, heterocytes). Cells cylindrical, barrel-shaped or spherical, shorter up to longer than wide, pale or bright blue-green or olive-green, containing aerotopes (subg. Dolichospermum) or without aerotopes, but sometimes with granular content (subg. Anabaena); terminal cells sometimes slightly elongated, conical, conical rounded or spherical, not vacuolized. Heterocytes spherical, widely oval or cylindrical, sometimes elongated, usually slightly greater than vegetative cells. Akinetes spherical,oval or cylindrical, solitary or several in a row, intercalar, developing always paraheterocytic, close to heterocytes from their both sides, or slightly distant from them.','Komárek (1992)',NULL,0,0),(82,144,'description','Cells solitary or in groups of twos after division, sometimes in irregular clusters, but never in colonies, without gelatinous envelopes, more or less cylindrical, rod- shaped with rounded ends up to widely oval, straight or slightly arcuate. Cell content homogeneous, without separation of centro- and chromatoplasma, but sometimes with lengthwise striation. Thylakoids situted in cells lengthwise; cell wall S-layer of square lattice (P4) was identified in <i>C. minervae</i> and <i>C. cedrorum</i>.','komárek & anagnostidis (1998)',NULL,0,0),(83,144,'description','Unicellular; cells solitary or in groups, oval, shortly cylindrical or irregularly cylindrical with widely rounded ends, without or with very fine mucilaginous layers around the cells. Cells usually pale blue-green to olive-green, mainly containing phycocyanin, with homogeneous content or with fine, dispersed granules, probably immotile, not forming filamentous involution forms. Probably with chromatic adaptation (?).','komárek (1992)',NULL,0,0),(84,157,'description','Heteropolar cells solitary or in groups, elongate, attached to the substrate by one end, long cylindrical when old, sometimes irregularly laterally or Y-shaped divaricate, at the base slightly widened-rounded and sometimes with short, cup- shaped, simple sheath (pseudovagina). Cell content pale blue-green, olive-green or light redaish, homogeneous or with solitary granules, usually with visible, separate chromatoplasma (lateral position of thylakoids). <br>','komárek & anagnostidis (1998)',NULL,0,0),(85,157,'description','Unicellular; cells elongated, narrow, cylindrical up to very long cylindrical, heteropolar, rounded at the apex and shortly widened: at the base, attached to the substrate by help of the very fine, cup-shaped, colourless, thin pseudovagina. The ˝filamentous˝ cells are sometimes in the upper part asymmetrically pseudodichotomously divaricated, at the ends with developed rows of daughter cells - exocytes. Cell content pale blue-green, thylakoids in cells concentrically arranged along the cell walls.','komárek (1992)',NULL,0,1),(86,165,'description','Filaments free-floating, solitary, straight, bent or screw-like coiled, in several species narrowed towards ends, without sheaths. Trichomes isopolar (heteropolar only in trichomes with only one heterocyte), subsymmetrical, with or without constrictions at cross-walls. Cells are cylindrical or barrel-shaped, usually distinctly longer than wide, pale blue-green, yellowish or olive-green, facultatively with aerotopes; end cells are conical or bluntly or sharply pointed. Heterocytes only terminal, oval, ovoid or conical, sometimes slightly curved and drop-like, unipored; they develop after ± asymmetrical division of the end cells, usually˝ asynchronously at both ends of the trichome. Akinetes are ellipsoidal or cylindrical, in coiled specimens usually slightly curved, developing usually slightly distant from heterocytes, rarely adjacent to apical heterocytes. Reproduction by trichome fragmentation and by akinetes. - Nine species are recently accepted (Fig. 3), but more morphotypes can be recognised, in future (comp. Fig. 2). ','komárek & komárková (2003)',NULL,0,0),(87,165,'description','The thin trichomes (<4 um in diameter) are straight or loosely coiled; vegetative cells are cylindrical and exhibit randomly distributed gas vesicle clusters. Heterocysts occupy exclusively terminal positions, at one or both ends of the trichomes. As the vegetative cells that give rise to them, heterocysts are conical to spear-shaped. Cylindrical akinetes, singly, in pairs or short chains, are formed adjacent to, or slightly distant from, the heterocysts. Sheath layers and hormogonia that differ structurally from the mature filaments are not produced.','castenholz (2001)',NULL,0,0),(88,165,'description','Planktonic; trichomes solitary, straight, slightly curved or spirally coiled, sub-symmetric structure; gas vesicles present; mucilaginous envelope absent. Heterocytes conical or long ovoid in shape, always terminal at one or both ends of the trichome developing from asymmetric division of the apical cell; the ends of the trichome attenuated when heterocytes not present; vegetative cells cylindrical with little or no constriction at the cross-walls; akinetes cylindrical or oblong-ovate, solitary or in pairs, intercalary, generally near to but remote from the heterocytes with para-heterocytic development.','baker & fabbro (199933):',NULL,0,0),(89,165,'description','Up to now, known species of the genus <i>Cylindrospermopsis</i> have been found only in freshwater plankton. The main diacritical features, characterizing this genus among nostocacean cyanobacteria, are as follows (Fig. 2):<br> (1) The filaments are isopolar, solitary, straight or coiled, free floating,cylindrical or slightly narrowed toward both ends. This feature is identical with the genus <i>Aphanizomenon</i>, from which it differs, however, by the mode ofheterocytedevelopment.<br> (2) The heterocytes develop only from terminal, narrowed cells, after asymmetrical cell division from the apical smaller part. From this point of view, the most related genus is <i>Anabaenopsis</i>, in which the heterocytes also divide from smaller cells after asymmetrical division. This division proceeds always intercalarly, two heterocytes being formed from two neighbouring cells, situated in a mirror-like position (the terminal position of heterocytes in <i>Anabaenopsis</i> is only secondary, after the disintegration of the trichome between two heterocytes). The apical heterocytes in <i>Cylindrospermopsis</i> do not usually develop simultaneously at both trichome ends, but one after another (Fig. 2,1-II).<br> (3) The akinetes develop facultatively beside or slightly distant from heterocytes, solitarily, in pairs, or in short series. The development of akinetes with combination with heterocytes gives to the <i>Cylindrospermopsis</i> filaments a typical subsymmetric appearance. Of the other related genera, only the genus <i>Aphanizomenon</i> has subsymmetric trichomes, but the heterocytes develop intercalarly at several places from one vegetative cell. The genus <i>Anabaenopsis</i> has a typical metameric structure. Another genus, in which the heterocytes develop at both trichome ends (but not after an asymmetrical cell division) is <i>Cylindrospermum</i>, which has, however, typical symmetrical trichomes (with terminal heterocytes and akinetes developing symmetrically beside heterocytes).','komárková (1998)',NULL,0,0),(90,165,'description','Filaments solitary, straight or screw-like coiled, free-floating, slightly narrowed to the both ends, without sheaths; trichomes isopolar (or secondary heteropolar - transient stages), with slight .constrictions or unconstricted at cross-walls, subsymmetric (according to the position of heterocytes and akinetes). Cells cylindrical, isodiametric or shorter or longer than wide, pale blue-green or yellowish, with aerotopes; end cells (before heterocyte formation) narrowed, conical, bluntly pointed. Heterocytes ovoid or conical, sometimes slightly curved, unipored, terminal; they develop from the terminal cells, which change into proheterocytes after asymmetrical cross division of the end cell in a young trichome. Akinetes oval to cylindrical with rounded ends, developing asymmetrically on a trichome, solitary or in short rows (up to three), slightly distant from the terminal heterocytes, rarely close to heterocytes.','komárek (1992)',NULL,0,0),(91,165,'description','Trichomes straight or spirally coiled tapering slightly towards the ends; cells cylindrical with little or no constrictions at the crosswalls; heterocysts always terminal, when the trichomes break new heterocysts arise at the free ends of the trichomes by the transformation of the end vegetative cells; spores present intercalary in position','seenayya et subba raju(1972)',NULL,0,0),(92,107,'description','Filamentous; filaments simple, unbranched, rarely solitary, usually joined and tangled in fine, diffluent mats, microscopic, or later macroscopic, forming blue-green layers. Trichomes without mucilage, without sheaths, at cross walls unconstricted or slightly constricted, isopolar, slightly irregularly waved, narrow, 0.8-5 /um wide, uniserial, more or less cylindrical up to the ends,. immotile. All cells cylindrical, after division more or less isodiametrical or slightly shorter than wide, later up to 5-times longer than wide, without aerotopes, sometimes with several prominent granules within protoplast, with thylakoids arranged concentrically along the cell walls; end cells widely rounded or obtuse. Swollen involution cells appear in trichomes in dependence on the environmental conditions. Cell content intensely blue-green, without phyco-erythrin. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(93,110,'description','Filamentous; filaments solitary or in groups or clusters, rarely in mats, slightly irregularly coiled, sometimes more or less parallel oriented, with firm, distinct, colourless sheaths enveloping one (rarely two) trichomes, opened at the ends (only exceptionally they occur young trichomes without sheaths). Trichomes of the same width along the whole length, not attenuated towards the ends, constricted at the cross walls, uniserial, isopolar, metameric (With several heterocytes<br> developing regularly in certain distances from one another along the trichome). Cells cylindrical or barrel-shaped, more or less isodiametrical up to longer than wide, blue-green, pale greyish-blue, olive green or reddish, very rarely with scarce aerotopes, usually with prominent granules; terminal cells not elongated, rounded. Heterocytes spherical, oval or cylindrical, usually of the same width or slightly greater than vegetative cells. Akinetes usually elongated, oval up to cylindrical, rarely spherical, developing always apoheterocytic (in rows between two heterocytes, and successively towards heterocytes), sometimes irregularly.','Komárek (1992)',NULL,0,0),(94,106,'description','Colonies multicellular, micro- to macroscopic (up to several centimeters in diameter), with cells arranged irregularly, loosely or densely in common mucilage, gelatinous, spherical or (usually) amorphous, greenish, blue-green or brown. Common mucilage fine, colourless, homogeneous and diffluent (subg. <em>Anathece</em>), or distinct, delimited, more or less smooth on the surface, structureless (subg. <em>Cyanogastrum</em>), or in marginal parts lamellate and yellowish or yellow- brown (rarely reddish), with cells in their own indistinct or distinct and/or lamellose, delimited envelopes (subg. Aphanothece). Cells widely oval to cylindrical (rod-shaped) with rounded ends, rarely oval-fusiform, straight or slightly arcuate, sometimes with clearly visible chromatoplasma; in a few planktic species solitary aerotopes occur facultatively.<br>Cell division by binary fission (mainly cleavage) in one plane in &nbsp;successive generations, perpendicular to the longitudial cell axis; In &nbsp;several species the daughter cells shift immediately after the division &nbsp;from the longitudinal position, giving the impression of \'oblique\' or &nbsp;\'longitudinal\' division. In several species facultative nanocyte &nbsp;production has been recorded. Reproduction by fragmentation of colonies, &nbsp;sometimes even into solitary cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(95,106,'description','Unicellular - colonial; colonies many-celled, micro- or macroscopic (up to several cm in diameter), mucilaginous, irregularly spherical or irregular, with cells irregularly, scarcely or densely arranged through the whole colony, greenish, bluish, brownish or reddish coloured; colonial slime diffluent or (rather) limited, usually without structure, colourless or near the surface yellowish, yellow-brownish or reddish coloured (particularly in aerophytic species); cells quite without own mucilaginous envelopes (subg. <i>Anacystis</i>) or facultatively (especially in the marginal parts of colonies) with their own, fine, sometimes concentrically lamellated mucilaginous envelopes (subg. Aphanothece). Cells widely oval, oval, ellipsoidal or rod-like, straight or slightly curved, with rounded ends, in one species with facultative aerotopes, pale greyish plue-green, pale to bright blue-green or reddish, sometimes with visible chromatoplasma (peripheral location of thylakoids).','komárek (1992)',NULL,0,1),(96,106,'description','Zellen ellipsoidisch bis zylindrisch-stäbchenförmig, gerade oder leicht gekrümmt, zu vielen in mehr oder weniger formlosen, gallertartigen bis schleimigen Lagern vereinigt, in homogener Gallerte, manchmal mit engen oder blasigen, niemals ineinander-r geschachtelten, aber manchmal geschichteten Hüllen, welche mehr oder weniger zerfließen. Teilung quer zur Längsachse. Zellen regellos nach allen Raumrichtungen gelagert. Gelegentlich Nannocytenbildung.','Geitler (1932)',NULL,0,1),(97,108,'description','Filamentous; filaments unbranched, solitary and free living (floating), or in mats which are microscopic or macroscopic, covering the substrate, more or less regularly screw-like and more or less freely coiled along the whole length, with unchanged or continually changing (decreasing or increasing) width of screws; trichomes:spirals width ratio = (2.5)-5-(10). Sheaths usually missing, rarely facultatively developed, colourless, tube-like, joined to trichomes, opened at the ends, containing always only one trichome. Trichomes isopolar, 3-10 jum wide, uniserial, composed from cylindrical cells, constricted br unconstricted at the visible cross walls, not attenuated or slightly attenuated towards the ends, motile (rotation). Cells without aerotopes or (in planktic species) with aerotopes, more or less isodiametric or shorter than wide, sometimes granular and with condensed granules at the cross walls; end cells widely rounded and usually with thickened outer cell walls or with calyptras (in developed trichomes); special perforation of cell walls (cross walls and side walls; see in Guglielmi et Cohen-Bazire 1982; all species?). Cell content pale or bright blue-green or olive green; thylakoids situated perpendicularly and irregularly along the cell walls. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(98,109,'description','Cells solitary, in few-celled groups or in more or less spherical, microscopic colonies, forming granular mats. Cells or their groups enveloped by distinct, delimited, usually firm sheaths, which are colourless or coloured by sheath pigments (reddish, yellow, etc.), and covered by irregularly, but evenly distributed, conical or rounded wart-like processes and forming granular or spiny surface of their colonies. Cells subspherical, oval or irregular in outline, sometimes slightly elongated or polygonal-rounded. Common envelopes thin or thick, with the surface covered by minute or stout, wart-like projections of different length.','Komárek et Anagnostidis (1998)',NULL,0,0),(99,109,'description','Unicellular - colonial; colonies more or less spherical, in irregular agglomerations which form grumose, gelatinous, reddish, olive-green, yellow to golden yellow or brown, or light bluish mass, later macroscopic; colonial envelopes thick, stiff, with confluent layers at the margin, colourless, yellow or pink, up to yellowish brown or dark brown; surface of gelatinous envelopes both of individual cells and colonies covered by minute or stout wart-like projections of different length; cells enclosed in the thick-sheathed own envelopes, lamellated or not, not confluent. Cells spherical, oblong or more or less irregular, enclosed in 2-4-8-16 in one special colony; cell content homogeneous or finely granular, without aerotopes, olive green, bright blue-green or brownish green.','komárek (1992)',NULL,0,1),(100,112,'description','Filamentous; filaments simple, straight or waved, with true branching, enveloped by a calcified sheath (envelope), solitary or in free clusters, creeping on the substrate. Trichomes uniserial, cylindrical, of the same width along the whole length, narrow, without constrictions at cross walls; true branching lateral (usually unilateral); type of branching: T-type. Cells cylindrical, longer than wide, end cells cylindrical and rounded at the apex. Heterocytes lateral or at the end of short, l-celled or several-celled branches, which are morphologically identical with main trichomes; they occur rarely in an intercalar position. Akinetes not known.','Komárek (1992)',NULL,0,0),(101,111,'description','Cylindrical cells are arranged more or less in parallel (lengthwise, in one direction) in narrow, filamentous or tubular, elongated mucilaginous colonies, tapering and pointed or open at both ends. Cells are slightly distant, but not in rows or in pseudofilaments. The mucilage is fine, homogeneous, colorless, and usually distinctly delimited at the margin. Cells are always cylindrical, straight, with rounded ends, solitary or in pairs after division, pale blue-green, (2.2)3-15(20) X 0.5-3 μm. Cells divide perpendicularly to the long cell axis in two, more or less isomorphic daughter cells.','komárek (2003)',NULL,0,0),(102,111,'description','Colonies mucilaginous, elongate, in the form of tubular sheaths, more or less tapering and (sometimes) pointed (rarely rounded) or open at both ends; slime homogeneous, fine, colourless, enveloping numerous, more or less lengthwise and parallely to the longitudinal axis (axial core) oriented cells, but without regular arrangement (not in rows or in pseudofilaments); cells slightly distant from one another, only after division two together for a short time. Colonies sometimes joined into an amorphous, clathrate thallus. Cells cylindrical, rod- shaped, with rounded ends.','komárek &amp; anagnostidis (1998)',NULL,0,0),(103,111,'description','Zellen lang zylindrisch, gerade, in farbloser, homogener Gallerte lose gelagert, einen zylindrischen, weit ausgebreiteten, mehr oder weniger zerrissenen Thallus bildend. Zellteilung nach einer Raumrichtung. </u></u></u></u>','Geitler (1935)',NULL,0,1),(104,115,'description','Filamentous-thallic; thallus thin, flat, felt-like. Filaments free, tangled, creeping, regularly and Tolypthrix-like false branched, with single branches; older filaments thick, enveloped by a thick, lamellate sheath, younger filaments with thin, homogeneous sheath. Trichomes uniserial, old ones torulous, deeply constricted at cross walls, rarely with true branching, irregularly waved, with more cylindrical young trichomes and young branches, slightly attenuated towards the ends. Cells isodiametric or slightly shorter or longer than wide, without prominent inclusions. Heterocytes develop intercalary, after alse branching remain often at bases of branches, oval or more or less spherical. Old trichomes change often in chroococcoid stages. Akinetes not known.','komárek(1992)',NULL,0,0),(105,114,'description','Filamentous; solitary filaments or small groups of trichomes. Trichomes with a limited growth, usually short (with up to 16 cells/trichome), 0.5-7 μm wide, uniserial, unbranched, more or less straight or slightly curved, isopolar, not attenuated to the ends, mainly constricted, rarely unconstricted at the cross walls. Sheaths lacking, sometimes (facultatively) with fine mucilage enveloping trichomes. Immotile, rarely with indistinct trembling of trichomes. All cells morphologically and functionally identical, isodiametric or slightly shorter or longer than wide, cylindrical up to barrel-shaped, end cells widely rounded; thylakoids probably concentrically arranged along the cell walls. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(106,114,'description','Trichomes of <i>Borzia</i> are without a gelatinous sheath and are usually composed of 3 to 8 cells. Terminal cells of a trichome are hemispherical, and other cells are barrel-shaped This genus may be looked upon as one that is in a permanent hormogonial condition.','Smith (1950:575)',NULL,0,0),(107,116,'description','Filamentous - thallic; thallus flat up to hemispherical, up to 5 cm in diameter, mucilaginous, sometimes crusty, hollow in the center when old, dark green or brownish, composed from horizontal layers of freely tangled or more or less parallely and radially (vertically to the substrate) arranged, true branched trichomes, without loop formations. Sheaths present in young trichomes, colourless or yellowish, absent and diffluent in old trichomes, but filaments enveloped by common, limited mucilage. Trichomes more or less cylindrical in the middle part, uniseriate; trichomes and branches toward the ends continually narrowed, sometimes up to the hairs with narrow,<br> elongated cells; old trichomes (in old parts of thallus) more freely coiled, thinner, with more elongated and more cylindrical cells; types of true branching: reverse V-type, rarely V-type. Heterocytes intercalar, spherical, barrel-shaped, sometimes shorter or longer than wide, usually wider than vegetative cells. Akinetes missing.','komárek (1992)',NULL,0,0),(108,117,'description','Filamentous - thallic; thallus irregularly cylindrical, mucilaginous up to filiform, attached by its basis to the substrate, narrowed to the apical end, divided in long, flexuous filamentous processi, up to 2 cm long and about 1 mm wide when old; later form gelatinous, layered mass; within mucilage numerous, irregularly tangled and freely coiled trichomes. Trichomes uni-serial, more or less cylindrical along the whole length, not attenuated towards the ends, clearly constricted at cross walls, torulous; trichomes irregularly true branched, branches morphologically identical with main trichomes; types of true branching: T-type, rarely V-type. Cells barrel-shaped, isodiametric or slightly longer or shorter than wide. Heterocytes present, solitary, intercalar, barrel-shaped. Akinetes unknown.','komárek (1992)',NULL,0,0),(109,119,'description','Filaments heteropolar, differentiated into basal (usually joined to the substrate) and apical parts, simple, solitary or in small groups, separated one from another (not in common mucilage), rarely with single, lateral false branches, oriented more or less in direction of the original growth; the filaments sometimes creeping on the substrate. Trichomes always with basal, more or less spherical or hemispherical heterocytes, and occasionally with intercalar cylindrical heterocytes; at intercalar heterocytes sometimes division of trichomes and their subsequent disintegration; trichomes sometimes with widened basal part, constricted or unconstricted at the cross walls, ending by the hair-like apical part composed from narrow, long, hyaline cells; the hair formation is dependent on phosphorus-metabolism; (trichomes in several species obligatory without hairs - they represent probably a special genus different from both the Calothrix and Microchaete). Sheaths always present, usually firm, sometimes lamellated and yellow-brownish coloured, or funnel-like widened at the ends; cells cylindrical or barrel-shaped. Aerotopes in vegetative cells absent, but occur in hormogonia (always 7). Akinetes rarely in basal parts (known in few species only). Probably able to chromatic adaptation (all species 7).','Komárek (1992)',NULL,0,0),(110,118,'description','Filamentous cyanobacterium, attached to solid (mainly subaerophytic) substrates, forming macroscopic, velvet-like strata, sometimes<br> composed from densely arranged, erect fascicles. Filaments ensheathed, intensely fasciculated, parallel situated, long, 12–26 um wide, cylindrical, of the same width along the whole length; Tolypothrix- or Scytonema-like false branching occurs sporadically, mainly in terminal parts of filaments. Sheaths thin or slightly thickened, sometimes slightly lamellate, colorless or yellow brown, at the ends roundly closed, open after hormogonia release. Trichomes cylindrical, not or very slightly constricted at cross walls, not attenuated toward ends. Cells of different length, very short (up to 1 ⁄ 5 of width) in hormogonia, apical parts of trichomes and in meristematic zones, up to longer than wide in old parts; apical cells morphologically identical with other vegetative cells, rounded at the apex. Heterocytes solitary, intercalary, discoid up to cylindrical, up to longer than wide. Without akinetes','fiore et al. (2007)',NULL,0,0),(111,120,'description','Filaments heteropolar, rarely straight and erect, usually creeping on the substrate, but distinctly divided into basal end with a heterocyte and the apical end, simple,unbranched, solitary or in small, microscopic groups. Trichomes with basal, more or less spherical or hemispherical heterocytes, occasionally also with intercalar, cylindrical heterocytes; at intercalar heterocytes sometimes division of trichomes and their disintegration; trichomes cylindrical, not attenuated, but sometimes with slightly widened apical parts, constricted at the cross walls. Sheaths always present, firm, thin, colourless, open at the ends. Cells cylindrical or barrel-shaped, sometimes more rounded at the ends, without aerotopes, but sometimes with a granular content, blue-green, yellowish or pale greyish-blue. Akinetes not well known.','Komárek (1992)',NULL,0,0),(112,122,'description','Cells heteropolar, slightly elongate, more or less club-shaped, attached to the substrate individually by their narrower ends, solitary or in groups, always enveloped by a thin (rarely a little thickened), firm, colourless sheath (pseudovagina); Joined to the substrate by the narrow base or by a pad (more or less discoid), which is a pan of a sheath. Pseudo vagina opens at the apex before the exocyte liberation. Cell content homogeneous (thylakoids are regularly distributed throughout the cell), usually pale blue-green, olive-green or reddish. Several marine and a few freshwater species are known. ','komárek & anagnostidis (1998)',NULL,0,0),(113,122,'description','Unicellular; solitary cells or groups of cells, joined by one end to the substrate. Cells always polarized, attached by one (basal, morphologically distinct) end to the substrate, usually by help of a pad or leg, and with free, widely rounded apical end; they are usually club-shaped, narrowed to the basis. Around cells firm, thin, sometimes layered sheaths, opened at the apex during the cell division (pseudovagina). Cell content grey, greyish blue-green, blue-green, yellowish or pinkish red, finely granular, always without aerotopes. Thylakoids probably peripherally situated.','komárek (1992)',NULL,0,0),(114,123,'description','Cells heteropolar, slightly or distinctly elongate, attached by their bases to the substrate (stones, plants), to the margin of sheaths of their mother cells or radially and more or less parallely arranged in gelatinous colonies; solitary cells, or micro- to macroscopic colonies, which are shrub-like, more or less spherical (with radially arranged cells in common mucilage) or flat (composed of a few layers of densely and parallely clustered cells). Cells spherical, later growing in club-shaped, cylindrical, pear-shaped, oval or ellipsoidal form; always enveloped by a sheath (pseudovagina), which is thin, colourless or slightly lamellate and yellowish or brownish, opening at the apex after cell division and exocyte separation, at the base usually narrowed and sometimes ending in an adhering pad (disc, sometimes with a very short stipe); the cells are sometimes slightly withdrawn from the base of a sheath; in some species the sheaths are diffluent forming a gelatinous mass, in which daughter cells remain enclosed. Cell content homogeneous, sometimes with distinguishable chromatoplasma (thylakoids are wavy, situated principially parietally but in several modifications, sometimes partly protruding into the centroplasma), in several species with prominent, solitary granules (cyanophycin, carboxysomes); cell content usually pale blue-green, yellowish, olive-green, greyish, pinkish or reddish-violet, sometimes almost colourless (the colour changes in numerous species in one and the same colony. ','komárek & anagnostidis (1998)',NULL,0,0),(115,123,'description','Unicellular; solitary, more or less elongated cells or groups of cells joined to the substrate /subg. <i>Chamaesiphon</i>/, or forming microscopic shrub-like colonies or layered, narrow mats with densely and parallely gathered cells on stones or submersed plants, perpendicularly oriented to the substrate /,subg: <i>Godlewskia </i>(Janczewski)Geitler 1925/. Cells always polarized, joined to the substrate with one (basal) end by means of a small mucilaginous pad (cells without pads occur only in upper parts of multilliyered colonies); cells oval, cylindrical or club-shaped, rounded at the apex. Around cells mucilaginous sheaths, fine and diffluent of firm and lamelaed; the sheaths open at the apex during the division process (pseudovaginae). Cell content grey, blue-green or pinkish, usually finely granular, always without aerotopes. Thylakoids localized peripherally, +/- concentrically, sometimes, moreover, with several central localized, coiled thylakoids','komárek (1992)',NULL,0,1),(116,121,'description','Thallous; thallus attached to the substrate, cushion-like, hemispherical or prostrate, up to several mm high, brownish or blackish, gelatinous, later confluent from more subcolonies, in the middle sometimes + concentrically layered, composed from basal, irregular, densely tangled trichomes (sometimes joined in a dense irregular cell mass - ˝chroococcal˝ stages), from which grow long, erected,parallely and densely gathered, radially oriented, true branched trichomes, with numerous, repeatedly<br> pseudodichotomously (rarely laterally) divaricated branches, growing +/- in the same radial direction. Branching types ˝Y˝ and ˝T˝. Trichomes uniseriate, constricted at cross<br> walls. Sheaths fine, thick, not or sometimes slightly lamellated, firm or diffluent, colourless or yellowish-brown. Cells subspherical, barrel-shaped, rounded-quadratic or rounded-polygonal, with blue-green content. Heterocytes intercalar or lateral, +/- ellipsoidal, with colourless or yellowish cell wall. Akinetes arise sporadically in basal parts, with firm, thick, brown cell wall.','komárek (1992)',NULL,0,0),(117,349,'description','Filamentous, colonial; trichomes free disposed within a mucilaginous colony. Colonies small, more or less spherical, up to 200 um in diameter, brownish, sometimes confluent in.gelatinous irregular mats. Trichomes irregularly curved or flexuous, uniseriate, unbranched, along the whole length of the same width, torulose, constricted at cross walls. Mucilage hyaline or brownish, gelatinous, homogenous, limited. Cells barrel-shaped, isodiametrical or slightly shorter than wide, with homogeneous content, pale blue-green; apical cells rounded, without calyptra. Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(118,125,'description','Thallous; thallus in form of a compact stratum of indefinite size, composed of irregular or irregular-rounded cell-packets and aggregates, or of uniserial up to multiserial short rows of cells (trichomes with 3-20 cells), usually without distinct mucimginous envelopes, but sometimes single cell-packets enclosed in thin, firm sheaths. Elongated branches or typical filaments not formed. Cells rounded or angular, with pale blue-green, granula content. Heterocytes terminal and intercalar, irregularly disposed, sometimes lacking. Akinetes not observed.','komárek (1992)',NULL,0,0),(119,124,'description','Colonies mucilaginous, multicellular, in outline more or less spherical, hemispherical, flattened or granular irregular<br> with rough surface, often composed of subcolonies, micro-, later usually macroscopic, attached to the substrate (plants, stones) or free-living, epipelic or metaphytic, sometimes forming a large gelatinous mass composed of single microcolonies. Cells irregularly arranged in common mucilage, but sometimes forming (particularly in marginal parts) short, irregular rows of cells, usually radially oriented; the rows are sometimes oriented perpendicularly to the substrate. Cells spherical or oval, in old colonies sometimes rounded<br> polygonal, without or with indistinct and diffluent, rarely distinct, delimited and firm individual mucilaginous envelopes, with blue-green, greyish, pale olive-green, yellowish or reddish, finely granular content.','komárek & anagnostidis (1998)',NULL,0,0),(120,124,'description','Colonies mucilaginous, microscopic, composed of distinct, parallely arranged and fasciculate rows of cells which are slightly distant from one another, situated within individual gelatinous, sometimes slightly lamellate, colourless envelopes, solitary or joined together and thus forming gelatinous «fascicles», which are sometimes attached by one end to the substrate; the mucilaginous envelopes<br> surrounding cells are confluent laterally, but rows («mucilaginous fascicles») are not enveloped by any common sheath or mucilage (rows of cells or their «fascicles» are located more or less separately). Cells spherical or subspherical, after division hemispherical, probably with homogeneous content. ','komárek & anagnostidis (1998)[sub lithocapsa]',NULL,0,0),(121,124,'description','Unicellular - colonial; colonies irregular, gelatinous, in outline more or less spherical, hemispherical or flat and grumose, micro- up to macroscopic, attached to the substrate or free living, epipelic or in metaphyton, sometimes form gelatinous masses composed from single microcolonies. Cells are arranged in common mucilage of colonies usually in rows (sometimes indistinct), sometimes radially or paral1ely oriented, usually without their own envelopes. Cells more or less spherical, ellispoidal or irregular, with blue-green, greyish, pale olive-green, yellowish or reddish, finely granular content. ','komárek (1992)',NULL,0,1),(122,124,'description','Unicellular - colonial; gelatinous colonies microscopic, composed from parallely disposed and fasciculated rows of cells, which are within colony enveloped by wide, slightly lamellated, colourless gelatinous envelopes and distant one from another; envelopes around cells confluent by their sides together, but common mucilage around the colony is missing. Cells more or less spherical, after division hemispherical, probably with homogeneous content.','komárek (1992)[sub lithocapsa]',NULL,0,1),(123,124,'description','Zellen kugelig oder ellipsoidisch, meisy ohne deutliche Spezialhüllen, in gemeinsamer Gallerte zu afrechten oder radiären, meist undeutlichen Reihen angeordnet, zu mehr oder weniger halbkugeligen oder flachen und höckerigen, unregelmäßigen, festsitzenden Lagern vereinigt, welche manchmal aus Teilkolonien zusammengesetzt sein können. Zellteilungen nach drei Raumrichtungen, aber meist mit Betonung einer bestimmten Raumrichtung. Nannocyten bei einer Art bekannt.','Geitler (1932)',NULL,0,1),(124,124,'description','Kolonien aus parallelen Zellreihen nach drei Raumrichtungen gebildet und aus bis 130 u langen, bis 95 p breiten Bündeln zusammengesetzt, ohne gemeinsame Gallerthülle. Zellen kugelig oder ellipsoidisch, nach der Teilung oft halbkugelig.','Geitler (1932)[sub <i>Lithocapsa</i>]',NULL,0,1),(125,126,'description','Thallous; thallus micro- or macroscopic, prostrate, mucilaginous or slightly cotton-like, sometimes incrustated by calcium-carbonate, composed from free, +/- tangled filaments. Sheaths fine, thin, colourless or yellowish, sometimes indistinct. Trichomes always uniseriate, with lateral true branches (T-type), cylindrical or torulous when old; branches arise mainly from one side, cylindrical at the base, torulous in the middle and again cylindrical and narrowed to the apex. Cells in torulous part barrel-shaped, usually isodiametric or slightly longer or shorter than wide, in other parts long-cylindrical. Heterocytes usually commonly present, intercalar, solitary, more or less cylindrical. Akinetes not proved.','komárek (1992)',NULL,0,0),(126,104,'description','Filamentous; filaments free-floating, solitary, only in few species joined into fascicle-like, microscopic or macroscopic (up to 2 cm long) colonies with parallely oriented trichomes; trichomes straight, slightly curved or slightly coiled, along the length cylindrical or sharply or continually narrowed to the ends, at cross walls not constricted or constricted, always without firm sheaths, several species with very fine, mucilaginous, diffluent and colourless envelope (?); trichomes uniserial, in the middle part usually cylindrical, isopolar, with distinctly elongated and sometimes vacuolized cells at ~ the ends, with the apical cells long, cylindrical and hyaline (at the end rounded or obtuse), or intensely elongated, narrowed, vacuolized up to hyaline and sharply or bluntly pointed, or conical, slightly elongated and only occasionally with small vacuoles (subgenera?); trichomes always subsymmetric, with 1-3 distant, intercalary developed heterocytes, which are localized subsymmetrically at the fully developed trichomes (shifted to one end of a trichome). Vegetative cells cylindrical or barrel-shaped, more or less isodiametrical or slightly shorter or longer than wide, pale blue-green or blue-green, usually with aerotopes, but several species facultatively or always without gas vesicles under special environmental conditions. Heterocytes barrel-shaped or cylindrical with rounded or obtuse ends, which can completely disappear under special conditions (under high N-content). Akinetes rarely spherical or widely oval, usually oval to long, cylindrical with rounded ends, developing raheterocytically, solitary or in short rows (in two or three), close to heterocytes or slightly,; distant from them, usually in asymmetrical position in a trichome. Vegetative cells divide cross-wise and grow to the original size before &nbsp;the next division; terminal cells not capable to divide; without &nbsp;meristematic zones. Reproduction by trichome disintegration and by &nbsp;akinetes.','Komárek (1992)',NULL,0,0),(127,127,'description','Cells solitary or in more or less spherical or irregular groups, with thin, firm, colourless sheaths, usually periphytic on a variety of aerophytic or submersed substrates. Cells spherical, hemispherical or irregular-rounded, enveloped by sheaths. Without pseudofilamentous stages. Thylakoids distributed usually irregularly throughout the protoplast. Cell wall S-layer of special ribbon-like type found in two strains (Budel & Rhiel 1985).','komárek & anagnostidis (1998)',NULL,0,0),(128,127,'description','Unicellular; spherical cells, rarely solitary, sometimes gathered in free living irregular agglomerations or forming more or less spherical or irregular colonies. Cells or small groups of cells are enveloped by thin, firm, colourless, sometimes slightly layered sheaths (envelopes), which split during the liberation of daughter cells. Cells spherical or irregular spherical, with a blue-green, yellowish, greyish or reddish content, sometimesslightly granular. Thylakoids usually distributed irregularly , over the whole cell volume.','komárek (1992)',NULL,0,0),(129,128,'description','Unicellular - colonial; small agglomerations of cells, irregularly localized in fine, diffluent, colourless, sometimes slightly lamellated mucilaginous envelopes; colonies microscopic, but sometimes form macroscopically visible gelatinous masses. Cells spherical, hemispherical, irregular spherical, oval, more or less rounded, usually of different size in one colony, rarely irregular, blue-green; usually without own mucilaginous envelopes.','komárek (1992)',NULL,0,0),(130,130,'description','Unicellular - colonial; colonies usually microscopic, only few-celled, more or less spherical, rarely many-celled, forming macroscopic, gelatinous mats; colonial slime fine, diffluent, homogeneous and colourless or lamellated, limited and (rarely) coloured; around gathered cells special own envelopes, usually copying the shape of cells, homogeneous or lamellated (up to rich lamellated) [subg. Chroococcus], or the old envelopes diffluent and the cells remain distant from one another [subg. Limnococcus]. Cells rarely spherical (young reproduction cells), usually hemispherical up to irregular (often in a form of a sector of a sphere), with homogeneous or granular content, sometimes with several prominent granules visible in light microscope, pale or bright blue-green, yellowish, pinkish or violett, rarely with aerotopes (in some planktic species); sometimes (particularly in species with larger cells) with visible chromatoplasma (thylakoids are concentrated on the periphery of cells).','komárek (1992)',NULL,0,0),(131,130,'description','Zellen kugelig, nach der Teilung halbkugelig bzw. quadranten-und oktantenförmig, selten einzeln, meist zu 2, 4, seltener bis zu 16 oder noch mehr in Kolonien beisammen, mit homogenen oder geschichteten, deutlich ineinander geschachtelten, aber nicht wie bei Gloeocapsa blasig aufgetrieben und sehr deutlich gegeneinander abgegrenzten Hüllen. Bei manchen Arten (Gruppe II la) liegen mehrere Zellen in einer gemeinsamen, homogenen Gallerte. Teilungen abwechselnd nach 2 oder 3 aufeinander senkrecht stehenden Raumrichtungen; spätere Teilungswände meist schief orientiert, wenn die Tochterzellen nicht früher auseinanderfallen. Tochterzellen normalerweise zu vieren quadratisch oder würfelig gestellt, in vielzelligen Kolonien in der Regel sekundär verschoben oder durch schiefe Teilungen von Anfang an anders gelagert. Meist deutlicher Rhythmus zwischen Wachstum ohne Teilung und Teilung ohne Wachstum. Nannocytenbildung anscheinend selten.','geitler (1932)',NULL,0,0),(132,129,'description','Unicellular - colonial; solitary cells or (rather) dense agglomerations or groups and/or pseudofilamentous rows of cells, not polarized (only initial stages), spherical or irregular, polygonal with rounded ends, sometimes slightly flattened from sides and of different size, enveloped by thin, firm, layered, colourless sheath (envelope). End cells in pseudofilaments or solitary cells sometimes club-shaped. Cell content blue-green, olive-green or reddish, with solitary granules. Chromatic adaptation. ','komárek (1992)',NULL,0,0),(133,129,'description','Thallus aus haufenartig dicht beisammenliegenden, selten auf ganz kurze Strecken undeutlich fadenförmig und aufrecht angeordneten Zellen bestehend; Zellen oft einzeln, isoliert liegend. Zellmembran dick, oft geschichtet. Endosporen zu vielen (bis 64?) in vergrößerten Zellen gebildet.','geitler (1932)',NULL,0,0),(134,131,'description','p. 307: Unicellular cyanobacterium with bladder-like cells typically packed as duplexes, or in extracellular polymeric substance covered clumps and small chains without the ability to produce baeocystes. No growth without added combined nitrogen occurred. While requiring<br> relatively large amounts of iron for growth (>40 uM), the isolate was shown to facilitate removal of iron from culture media.; p. 310-311: The isolate is a unicellular cyanobacterium with cells typically packed as duplexes, or in clumps or small chains (Figs. 3 and 4), covered with extracellular polymeric substance (EPS). Cells exhibit oval shape (average longitudinal diameter of 4 ± 0.77 μm, and average transverse diameter of 3.3 ± 0.64 μm; n = 10). Micrographs (Figs. 3-5) indicate a bladder-like shape, similar to that of Synechocystis PCC 6803 cells. Although the morphology of 5.2 s.c.l cells is reminiscent of the <i>Synechocystis</i> genus, a salient difference is that isolate 5.2 s.c.l has a EPS cover, visible on SEM and TEM micrographs as a 0.3-0.4 μm skin-like envelope. ... EPS envelope of single 5.2 s.c.l cells may reach; ~1 μm, suggesting its importance to adhesion of 5.2 s.c.l cells to surfaces. ... This finding, as well as its pronounced capacity to<br> form biofilms on culture flask walls (data not shown), suggests that isolate 5.2 s.c.l is a sessile organism.','Brown et al. (2005)',NULL,0,0),(135,103,'description','Filamentous; filaments solitary or in free clusters with several tangled trichomes, free floating, along the length of the same width, without (rarely) or with constrictions at the cross walls, straight, arcuated or irregularly screw-like or spirally coiled, without sheaths, but sometimes with very diffluent, colourless, homogeneous slimy envelopes (staining!); trichomes originally metameric (the heterocytes develop intercalary in pairs in certain distances one from another), but<br> trichomes often disintegrate soon after heterocyte formation between heterocytes, the position of which i,s finally terminal in short disintegrated fragments of an original trichome (usual stage of population). Cells cylindrical or barrel-shaped, shorter up to several times longer than wide, pale blue-green, usually containing aerotopes facultatively missing). Heterocytes develop after the asymmetrical, mirror-like division of two neighbouring proheterocytic cells, spherical or widely oval, rarely ovoid or elongated, rounded conical, usually slightly greater than vegetative cells. Akinetes spherical or oval, solitary or several in a short row, intercalar (rarely occur terminal<br> after disintegration of trichomes), arise always paraheterocytic, but usually a slightly distant from heterocytes.','komárek (1992)',NULL,0,0),(136,132,'description','Cells solitary or in groups, heteropolar, attached to the substrate by their basal ends, elongate, ovoid, ellipsoidal, pear-shaped to cylindrical, widely or narrowly rounded at their bases, more or less narrowed to the apex and extended into a fine gelatinous hair; cells with homogeneous content. Mucilaginous sheaths (pseudovagina) thin, firm, sometimes slightly and indistinctly lamellate.','komárek & anagnostidis (1998)',NULL,0,0),(137,132,'description','Unicellular; solitary elongated cells, rarely grouped together, joined more or less perpendicularly by one (basal) end to the substrate, usually to filamentous algae or submerged water plants. Cells always polarized, attached to the substrate by the narrowed mucilaginous pad, on the apical end also narrowed and prolonged into thin mucilaginous hair-like string (sometimes long); cell-form widely oval, ellipsoidal, ovoid or pear-shaped, rarely slightly club-shaped. Around cells sometimes thin, mucilaginous, often diffluent, colourless sheaths (pseudovaginae), which open at the top during the cell division, if remained. Cell content pale blue-green, usually without visible granules, always without aerotopes.','komárek (1992)',NULL,0,1),(138,135,'description','Colonies microscopic, more or less spherical, up to 500 um in diameter, freeliving, enveloped by colourless, fine, homogeneous mucilage. Cells spherical or oval before division, situated more or less in the colonial periphery in one layer, each surrounded by its own, narrow, delimited gelatinous envelope, with more or less homogeneous or slightly granular content. ','komárek & anagnostidis (1998)',NULL,0,0),(139,135,'description','Unicellular – colonial; colonies microscopic, spherical or composed from several subcolones, free floating, enveloped by<br> mucilaginous, colourless, fine but more or less limited envelope, without any inner stalk system, with cells arranged peripherally in one layer, and ˝hollow˝ (?) in the centre. Cells spherical or slightly irregular elongated, usually surrounded by their own mucilaginous envelopes, sometimes of the unequal size, distant one from another, without aerotopes.','komárek (1992)',NULL,0,0),(140,133,'description','Colonies microscopic, mucilaginous, flat, tabular, with cells irregularly distributed in one layer (without forming<br> rows perpendicular to one another). Mucilage colourless, homogeneous, with irregular outline. Cells spherical, without individual gelatinous envelopes.','Komárek & Anagnostidis (1998)',NULL,0,0),(141,133,'description','Unicellular - colonial; colonies free living, microscopic, table-like or flat and waved, with irregular outlines, with cells arranged irregularly (not in perpendicullir rows) in one plane (layer), with usually greater amount of cells; common mucilaginous envelope is colourless, fine, diffluent at the margin; cells without own mucilaginous envelopes. Cells spherical, after division shortly hemispherical, with homogeneous, pale blue-green content, without aerotopes.','Komárek (1992)',NULL,0,1),(142,133,'description','Zellen kugelig, zu flachen, tafelförmigen, freischwimmenden Kolonien vereinigt, unregelmäßig (nicht wie bei Merismopedia in Längs- und Querreihen) angeordnet, in gemeinsamer Gallerte. Zellteilung nach zwei Raumrichtungen.',' Geitler (1932)',NULL,0,0),(143,134,'description','Cells are arranged more or less peripherally in one or a few layers (may be variable) near the surface of the microscopic, spherical, free-living colonies, which are sometimes composed of subcolonies. Colonial mucilage is fine, homogeneous, colorless, and usually diffuse at the margin, but usually more densely clustered in the center. Cells in young colonies are randomly and sparsely distributed, distant and variably arranged, and usually slightly shifted from one layer; later cells are arranged distinctly peripherally, forming one to three irregular layers. Cells are slightly elongated, widely oval to almost spherical, and radially situated in the colony (generic feature), pale blue-green or olive green, and 1-6.5 X 0.8-4 μm. One species (C. minimum) has distinct aerotopes (gas vacuoles). Cell division occurs in two planes in successive generations, perpendicular to one another and more or less to the colony surface. Reproduction is by disintegration of colonies.','Komárek (2003)',NULL,0,0),(144,134,'description','Colonies microscopic, more or less spherical or irregular spherical, sometimes compound, free floating, enveloped by fine, colourless, diffluent, very often indistinct, rarely distinct delimited mucilage. Cells in young colonies randomly and more or less sparsely disposed, diverging slightly radially from one another, in old colonies concentrated in the peripheral layer or up to three layers thick. In the center of colonies is a condensed cluster of slime, from which radiate irregular, fine and diffluent stalks or protuberances, which very soon disappear (staining !); in the center of old colonies fine slime. Cells slightly elongate, situated more or less radially in the outer layers.','Komárek & Anagnostidis (1998)',NULL,0,0),(145,134,'description','Unicellular - colonial; colonies microscopic, spherical, oval or irregularly spherical, mucilaginous, free living (floating or in metaphyton) in freshwater reservoirs, enveloped by colourless, fine and diffluent mucilaginous envelopes; cells are situated +/- radially and +/- irregularly in one to 3 layers on the periphery of colonies. Cells slightly elongated, widely oval, obovoid or almost spherical, radially and (in old colonies) densely arranged, without aerotopes, greyish blue-green, bright blue-green or olive green, finely granulated. Mucilaginous envelopes unstructured, but particularly in young colonies the dense mucilage clusters (irregular, fine, diffluent stalks) are in the centre of colonies (the cells are joined to the lobes of this cluster); this central mucilaginous cluster later disappears.','Komárek (1992)',NULL,0,1),(146,136,'description','<i>Coelosphaerium </i>comprises free-living, spherical or oval mucilaginous colonies, in which the cells are arranged irregularly in one marginal layer (but sometimes slightly shifted to one another), or near the surface of the sphere. Colonies sometimes are composed of subcolonies. Mucilage is colorless and homogeneous. Cells are spherical, pale or bright blue-green, and 1-7 μm in diameter. One species has visible aerotopes. Cell division occurs in two planes in successive generations, perpendicular to one another and to the colony surface. Reproduction is by disintegration of a colonv and bv liberation of subcolonies.','Komárek (2003)',NULL,0,0),(147,136,'description','Colonies microscopic, more or less spherical or oval, sometimes composed of subcolonies, rarely irregular when old, free-living, usually floating in plankton, enveloped by fine, colourless, usually not sharply defined, sometimes indistinct mucilage; mucilage limited to just around the peripheral layer of cells or forming a gelatinous layer (margin) around cells. Cells more or less in one layer on the colonial periphery, spherical or hemispherical after division, usually slightly or distinctly distant from one another, with or without aerotopes. Mucilage homogeneous, fine, never structured, without any stalks in the colonial center.',' Komárek & Anagnostidis (1998)',NULL,0,0),(148,136,'description','Unicellular - colonial; colonies microscopic, spherical or composed, free living (mainly planktic), enveloped by colourless, indistinct or limited fine mucilage, without any inner stalk system, with cells situated in one layer near the surface of colony. Cells spherical, mainly distant one from another, peripherally situated, in old colonies more densely than in young ones, pale or bright blue-green, two species with aerotopes. ','Komárek (1992)',NULL,0,1),(149,136,'description','Zellen kugelig, elhpsoidisch oder verkehrt-eiförmig, während der Teilung oft leicht „herzförmig˝, zu hohlkugeligen, freischwimmenden Kolonien vereinigt, nicht auf deutlichen Gallertstielen sitzend, meist ohne oder mit undeutlichen Spezialhüllen. Kolonialgallerte häufig radiär gestreift. Zellteilung in den Kolonien nach zwei aufeinander senkrecht stehenden Raumrichtungen. Ausserdem Teilung der ganzen Kolonie.','Geitler (1932)',NULL,0,1),(150,105,'description','Colonies microscopic, more or less spherical, irregular or flat, in several species macroscopic, irregular, usually with numerous, sparsely or densely, irregularly arranged cells; colonial mucilage mainly colourless, more or less homogeneous with indistinct margin, or (particularly in macroscopic colonies) firm, formless, I but clearly delimited; cells without individual gelatinous envelopes or occasionially (in firm colonies) with narrow, diffluent individual envelopes. Cells more or less spherical, after division hemispherical, without aerotopes. Cell wall S-layer of hexagonal lattice (identified in few small-celled species).','Komárek, Anagnostidis (1998)',NULL,0,0),(151,105,'description','Unicellular - colonial; colonies many-celled, irregular, usually amorph, microscopic (mainly benthic, planktic,periphytic, meta- phytic) or macroscopic (periphytic, aerophytic, epipelic), gelatinous, with irregularly, loosely or densely distributed cells; mucilage colourless, fine, diffluent or limited (in small, microscopic colonies), rarely yellowish, brownish or bluish (mainly in macroscopic colonies); cells without own mucilaginous envelopes. Cells spherical, after division hemispherical, pale greyish-blue or blue-green, rarely bright blue-green or olive-green, sometimes with visible chromatoplasma (peripheral location of thylakoids), in planktic species rarely with aerotopes (revision I); sometimes with granular content or with several prominent granules.','Komárek (1992)',NULL,0,0),(152,105,'description','Zellen kugelig oder fast kugelig, meist zu vielen in formlosen, weichen, oft mehrere Zentimeter großen Gallertlagern vereinigt, meist lose gelagert, in farbloser, homogener Gallerte eingebettet, aber oft mit einer dünnen, mehr oder weniger zerfließenden Spezialhülle umgeben, welche auch um Tochterzellen (um zwei vier, seltener um mehrere) als gemeinsame Hülle ausgebildet sein kann. Ineinanderschachtelung der Hüllen kommt nicht (oder nur ganz ausnahmsweise) vor. Gelegentlich Nannocyten-bildung. Zellen regellos angeordnet.','Geitler (1932)',NULL,0,1),(153,138,'description','Thallous; thallus membranous, leathery or fibrous, macroscopic up to 1 mm high, composed from more or less free, horizontally growing, densely packed, slightly flexuous filaments of the same morphology, with true, laterally branching of trichomes, and from more or less erect, usually pseudodichotomously branched filaments (T- and V-types of branching); pseudodichotomous branches arise by longitudinal division of the apical cells, lateral branches of intercalar cells; filaments usually crooked, somewhat roughened, cylindrical. Trichomes +/- cylindrical, toralous, uniseriate, distinctly constricted at cross-walls, enclosed in colourless or yellow~brown, firm, thick, lamellated sheaths, with apical growth. Cells subcylindrical, barrel-shaped to ellipsoidal, longer than wide; end cells rounded, sometimes slightly up to distinctly enlarged. Heterocytes and akinetes were not observed.','komárek (1992)',NULL,0,0),(154,137,'description','Filamentous; filaments united into intensely branched, mucilaginous, polarized, up to 1 cm high, blue-green or brownish or reddish fascicles; sheaths branched, firm, thin or thick, often lamellated, opened at the apex, colour- less or yellow-brown, containing 1 to several trichomes. Trichomes polarized with basal, usually elliptical heterocytes, parallely oriented, falsely, branched, cylindrical, uniserial, constricted at the cross walls, to the ends not narrowed or only slightly narrowed; false<br>branching initiate at the intercalar heterocytes. Cells shortly barrel-shaped, end cells widely rounded. Aerotopes absent. Akinetes develop rarely near the trichome bases, solitary or in short rows.','Komárek (1992)',NULL,0,0),(155,139,'description','Filamentous; filaments unbranched, irregularly waved or coiled, solitary or in microscopic clusters; trichomes without or with fine, diffluent and facultative sheaths, isopolar, more or less equally wide along the whole length or slightly narrowed to the ends, clearly and obligatory flattened from sides, on the cross section oval, uniserial, slightly constricted or unconstricted at the cross walls, immotile. Cells more or less isodiametrical or slightly shorter or longer than wide, without aerotopes, with slightly granular and blue-green content. End cells widely rounded. Heterocytes and akinetes are missing.','komárek (1992)',NULL,0,0),(156,140,'description','Cells solitary, in pairs, or in amorphous aggregates, capable of producing large amounts of diffluent mucilage, spherical to elongated, with dispersed thylakoids in fasciculated packets, with high concentrations of urobilin-containing phycoerythrin lightharvesting pigments. Diazotrophic. Marine in tropical oceans.','Mareš et al. 2019',NULL,0,0),(157,145,'description','Cells solitary or in twos after division, not in colonies, small, usually about 1-2(4) um long and about 1(-3) μm wide, without gelatinous envelopes, oval, ellipsoid to shortly rod-shaped, usually with well visible chromatoplasma. Thylakoids are arranged panetally along the cell walls.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(158,145,'description','Unicellular; cells solitary or in groups, widely oval up to shortly cylindricalor shortly rod-like with rounded ends, usually small (+/- up to 2 um in diam.), without mucilage or with very narrow, fine gelatinous layer around the cells. Cells with blue-green, pale blue-green or pinkish cell content (dependent on the PC/PE ratio), immotile. Usually without ability of chromatic adaptation. Thylakoids probably located concentrically near the cell wall. GC-content of the DNA = approx. 66-71 mol. percent. Without filamentous involution cells. Obligatory photoautotroph.','komárek (1992)',NULL,0,1),(159,141,'description','Nostocacean cyanoprokaryotic (cyanobacterial) taxonomic unit with isopolar, uniserial, unbranched filaments with heterocytes and akinetes. Trichomes solitary, without sheaths, free-tloating, or in fine, mucilaginous thallus, more or less straight or slightly flexuous, short (up to 80-120 um long), with terminal heterocytes on both isopolar ends, cylindrical, distinctly constricted at the cross-walls. Cells more or less spherical, barrel-shaped or slightly elongate or oval. Heterocytes terminal, spherical, ovoid or slightly oval, but developing intercalarly from one vegetative cell, which elongates, later symmetrically divides and from each daughter cell a heterocyte develops. Thus, the proheterocytes are originally situated in pairs in the intercalary position, but the trichomes quickly break at the junction between the young intercalary heterocytes. Akinetes arise next to the polar heterocytes, slightly distant from them by 1-2 vegetative cells, solitary or in short rows, or in the centre of short trichomes in chains; they are oval or oval-cylindrical.','komárek et al. (2010)',NULL,0,0),(160,143,'description','Colonies gelatinous, polarized, firm +/- «erect», ramified, macroscopically visible when old; ramification<br> is pseudodichotomous or irregular. Attached to the substrate. Cells in colonies arranged. irregularly or indistinctly radially. Cells irregular-rounded, more or less spherical, hemispherical, ellipsoidal or angulate- rounded, sometimes grouped 2-4 together in colonies; cells in marginal parts or at the apex of the colony sometimes indistinctly elongated. Around cells narrow, distinct envelopes. Colonial mucilage distinct, firm on the surface, confluent within colony.','Komárek & Anagnostidis (1998)',NULL,0,0),(161,143,'description','Unicellular - colonial; colonies gelatinous, polarized, firm, ramified, macroscopically visible when old; ramification is pseudodichotomous or irregular. Attached to the substrate. Cells in colonies arranged irregularly, or indistinctly radially. Cells irregular-rounded, more or less spherical, hemispherical, ellipsoidal or angulate-rounded, sometimes grouped 2-4 together in colonies; cells in marginal parts or at the apex of the colony sometimes indistinctly elongated. Around cells narrow, distinct envelopes. Colonial mucilage distinct, firm on the surface, confluent within colony.','Komárek (1992)',NULL,0,0),(162,142,'description','Trichomes free-floating, solitary, short or long, straight or coiled, cylindrical, slightly constricted or non-constricted at cross walls, up to 6 µm wide, clearly narrowed and pointed at the ends. Cells cylindrical, cell content finely granular and/or with facultative aerotopes; apical cells elongated, attenuated and acuminate, mainly colourless (hyaline). Heterocytes only intercalary, solitary, cylindrical or elliptical. Akinetes intercalary, solitary or rarely in twos, elongated ± cylindrical, distant from or aside heterocytes','Rajaniemi et al. (2005)',NULL,0,0),(163,147,'description','Colonies free floating with cells irregularly arranged in very fine slime, microscopic, irregular, with varying number of cells; in young colonies cells sometimes are arranged in irregular rows. Mucilage structureless, colourless, diffluent at the margin; cells without their own gelatinous envelopes, but often with brownish or blackish rings (ferric precipitates). Cells cylindrical, elongate with rounded ends, sometimes slightly arcuate.','komárek & anagnostidis (1998)',NULL,0,0),(164,147,'description','Unicellular-colonial; colonies free-floating, always microscopic, irregular in outline, with few or many freely, irregularly arranged cells, enveloped by very fine, indistinct, diffluent, colourless, wide mucilage, sometimes visible only after staining. Cells pale blue-green or pale grey, without gas vesicles, almost spherical up to cylindrical, straight or slightly arcuated, widely rounded at ends, with circular, blackish ferric precipitations on the cell surface and between cells; precipitations arise often at the place of cell division and remain sometimes free within common mucilage.','komárek (1992)',NULL,0,0),(165,146,'description','Filamentous, thalous; filaments more or less free living, not coalescing laterally in compact mats, irregularly branched, growing and intricated in caespitose, brownish thallus. Trichomes multiseriate with irregular lateral true branching; branches uniseriate or multiseriate, more or less short, often grouped together. Sheaths partly lamellated, hyaline to yellow-brownish. Cells in the main trichomes more or less irregular globose or shorter than wide. Heterocytes intercalar, localized usually in the marginal position in the multiseriate trichome, more or less globose.','komárek (1992)',NULL,0,0),(166,148,'description','Colonies free-floating. Cells solitary, in pairs or in short rows of four cells, irregularly distributed within the colonial mucilage. Solitary cells with a brown cap with semicircular outline at one end, probably consisting of ferric precipitates. Cell pairs or rows of four cells with a single cap or with a cap on either side. Cells very small, without aerotopes. Cell division by simple binary fission, with a single plane of division. Only one daughter cell has a cap immediately after cell division. Later, a new cap is formed at the opposite end of the other daughter-cell. Cells often rotate into an oblique or even parallel position after cell division.','Joosten (2006)',NULL,0,0),(167,150,'description','Cells solitary or in flattened or hemispherical groups (parallely or radially arranged), attached to the substrate; cells heteropolar, usually slightly or distinctly elongate, widely oval, obovoid, club-shaped or pear-shaped, rarely almost spherical or hemispherical, attached to the substrate more or less perpendicularly by the narrowed end and sometimes by discoidally widened sheath, or by widened base, at the apex rounded; in cultures only irregular groups of cells. Cells in colonies of variable size, with homogeneous, pale blue-green, olive-green or violet content. Sheaths (pseudovaginae) thin, firm, colourless.','Komárek & Anagnostidis (1998)',NULL,0,0),(168,150,'description','Solitary cells or groups of cells, joined by the basal end to the substrate. Cells more or less polarized, +/- spherical, oval or club-shaped, sometimes narrowed to the basis, attached to the substrate by the small gelatinous pad and by rounded basis; apical end widely rounded. Around cells firm, thin sheaths, later ˝opened˝ on the apical end (pseudovaginae). Cell content greyish blue-green, olive green or pinkish red, finely granular, always without aerotopes','Komárek (1992)',NULL,0,1),(169,149,'description','Colonies microscopic, solitary, free, with cells placed without any order in a mucilage. Cells elongated, with aerotopes, dividing logitudinally into equal parts.','Hindák (2002)',NULL,0,0),(170,156,'description','Colonies free-living, more or less irregularly spherical, globose or ellipsoidal, sometimes composed of subcolonies, with a system of mucilaginous, pseudodichotomously branched and structureless stalks, radiating from the center of colonies (staining!); common gelatinous material surrounding the whole colony not present. Cells more or less elongate, solitary and crosswise at the ends of divaricate stalks, more or less on the colonial periphery, without aerotopes, with parietally (concentrically) localized thylakoids.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(171,156,'description','Unicellular - colonial; colonies microscopic (up to 29 µm in diam.), free floating, more or less spherical, oval up to irregular, mucilaginous, with cells distant from one another, arranged more or less in a layer near the surface of the colony, connected by radially, pseudodichotomously branched, hyaline, mucilaginous stalks, radiating from the centre of the colony (staining !); the solitary cells are surrounded by a thin layer of mucilage, but the whole colony is not enveloped by a scarce, hyaline, diffluent slime. Cells elongated, slightly arcuated, with few peripherally and concentrically arranged thylakoids along the cell walls, joined to the stalks by their longer side, pale blue-green, yellowish green or greyish blue-green, without conspicuous inclusions or aerotopes.','komárek (1992)',NULL,0,1),(172,152,'description','Unicellular - colonial; mats on substrate, wide, thin, crustaceous, microscopic or macroscopic, composed from erected, parallel, pseudodichotomously or pseudotetrachotomously divaricated, short pseudofilaments, which are oriented more or less perpendicularly to the substrate; pswdofilaments enveloped by firm sheaths and are joined tightly together or confluent by their sides; from above they look as pseudoparenchymatous layer. Cells irregular, sometimes slightly elongated in the direction of pseudofilaments.','komárek (1992)',NULL,0,0),(173,151,'description','Unicellular - colonial; thallus in outline circular, attached to the substrate (red marine algae), composed from basal, discoid, blastoparenchymatous layer of cells and from more or less parallely oriented, erected short, straight, not divaricated and fasciculated pseudofilaments, each enveloped by its own thin and firm sheath; pseudofilaments are free, not confluent by their sides (sheaths) together. Cells irregular, in pseudofilaments elongated and at their ends widened, more or less spherical, blue-green.','komárek (1992, sub geitleriella)',NULL,0,0),(174,151,'description','Thallus in Sohle und aufrechte Fäden gegliedert. Sohle mehr oder weniger kreisförmig, aus kriechenden, radiär ausstrahlenden, dichotom (oder scheindichotom ?) verzweigten Fäden bestehend. Aufrechte Fäden kurz, gerade, parallel, unverzweigt, mit festen Membranen, seitlich nicht miteinander verwachsen. Sporangien terminal an den aufrechten Fäden. Endosporen durch simultane Teilungen gebildet.','geitler (1932, sub. nematoradaisia)',NULL,0,0),(175,151,'description','Thallus in Sohle und aufrechte Fäden gegliedert. Sohle mehr weniger kreisförmig, blastoparenchymatisch. Aufrechte kurz, gerade, unverzweigt, büschelig angeordnet, mit Membranen, seitlich nicht miteinander verwachsen, äjien terminal an den aufrechten Fäden.','geitler (1932, sub. radaisiella)',NULL,0,0),(176,155,'description','In colonies; colonies small, few-celled, microscopic, more or less spherical or subspherical, sometimes composed of subcolonies, with cells in short perpendicular rows, more or less distant from one another, sometimes three-dimensionally arranged within colonial slime. Mucilage fine, delimited or diffluent, colourless, forming wide margin around cells. Cells hemispherical, rectangular or cubicroundeii, without or with individual fine envelopes. Monotypic genus.  Komárek (1992): Unicellular - colonial; colonies microscopic (up to 150 um long), sometimes composed from subcolonies, irregularly oval, free living, with distinct, smooth or slightly diffluent, wide, colourless, mucilaginous envelopes; cells are arranged in rows containing (2)3 up to 9 or more cells in one row, for- ming later usually double-rows in one colony, or up to four parallel rows; the cells are sometimes enveloped by their own mucilaginous envelopes (this phenomenon results in slightly lamellated common mucilage); between the cells are remarkable spaces. Cells irregular, at the end of a row more or less rounded at the outer side, the inner cells rounded-cubic, more or less isodiametric, slightly flattened from sides; cells with blue-green, +/- homogeneous content or with solitary granules, without aerotopes. The arrangement of cells in rows is the most characteristical feature of this genus within the family Chroococcaceae.','Komárek & Anagnostidis (1998)',NULL,0,0),(177,154,'description','Colonies free floating, microscopic, subspherical to irregular in outline, mucilaginous, composed of a cluster of irregularly aggregated cells embedded within fine, homogeneous, colourless and diffluent slime. Ferric precipitates occur the gelatinous colonies. Cells spherical or subspherical, sometimes widely oval.','Komárek & Anagnostidis (1998)',NULL,0,0),(178,154,'description','Unicellular - colonial; colonies are free floating, microscopical, up to 40-celled, mucilaginous, +/- spherical up to irregular, embedded by a fine, homogeneous, colourless and more or less diffluent slime, with irregularly localized cells in the centre. In the centre of the cluster of cells is situated one large, more or less spherical grain, usually brownish with iron-oxid precipitations, or several small precipitations are spread through the colony; colonies without precipitations are rare. The cells are heaped around the central body or gathered into the ˝small groups, spherical, oval or shortly cylindrical, pale greyish blue-green, without gas vesicles.','Komárek (1992)',NULL,0,0),(179,158,'description','Thallus endolithic, penetrating into carbonate substrates, such as calcareous, marine littoral stones, rocks, ooid grains and mollusc shells, microscopic (to 85 um long), sometimes simply finger-like branched, composed of polarized groups of cells (= shortened heteropolar pseudofilaments). Cells solitary, in pairs or in groups (clusters) with up to 12 cells, usually more or less ovoid, pear-shaped or club-shaped, sometimes pear-shaped with remarkably elongate pedicell, on both ends rounded, enclose within ends of mucilaginous solitary, pseudodichotomous or finger-like branches of thallus, orientated by their narrowed ends to the ; surface of the upper substrate; the whole colony appears as a finger-like fascicle of pear-shaped cells immersed in the substrate. The gelatinous envelopes are firm, colourless or yellowish to yellow-brown, layered, narrowed and elongate toward the substrate surface, and provide the connection with the outer environment by a small opening. The varication of the thallus is caused by the lengthwise division of endolithic cells and cell clusters, and by the consequent directional production of gelatinous stalks. Cell content of variable colour greyish, bluish, olive-green, blue-green, red, pink), finely granular, without conspicuous inclusions. ','komárek & anagnostidis (1998)',NULL,0,0),(180,158,'description','Unicellular, sometimes forming polarized and specially oriented groups of cells. Thallus endolithic, penetrating in carbonate substrates in calcareous, marine littoral stones and rocks, microscopic, up to 85 um long, sometimes simply finger-like branched. Cells solitary, in pairs ot in groups (clusters) with up to 8 cells, more or less pear-shaped or club-shaped, on both ends rounded, enclosed within ends of mucilaginous finger-like branches of thallus, oriented by their narrowed ends to the surface of the substrate. The mucilaginous envelopes are gelatinous, firm, colourless, layered, narrowed and elongated toward the substrate surface, and provide the connection with the outer environment by a small opening. The branching is caused by division of endolithic cell clusters and through the consequent directional production of gelatinous ˝stalks˝. Cell content of variable colour (greyish, olive-green, blue – green, reddish), finely granular, without conspicuous inclusion.','komárek (1992)',NULL,0,0),(181,153,'description','Cells occur in spherical to irregularly reticulate, slimy, microscopic flat or three-dimensional colonies, which are sometimes elongate, composed from irregularly branching and anastomosing mucilaginous strands, later forming an amorphous mass with holes. The mucilage is fine, colorless, and sometimes diffuse. Cells are arranged in strands in one or more rows, and later irregularly. Cells are more or less spherical, slightly elongated to rod-shaped, small, up to 4.5 μm long (or diameter), without obvious gas vesicles, and pale blue-green, greyish, or olive green. Cell division is by binary fission, always perpendicularly to one (longer) cell axis. Daughter cells are isomorphic and grow to the original shape and size before the next division.','Komárek (2004)',NULL,0,0),(182,153,'description','Colonies free floating, initially more or less spherical, soon becoming irregularly reticulate, flat or three-dimensional, often elongate, composed of gelatinous, irregularly divaricate and anastomozing strands, with uniseriate, in older stages multiseriate rows of cells. Mucilage structureless, colourless, usually indistinct and diffluent at the margin. Cells spherical or slightly elongate, without prominent inclusions.','Komárek &amp; Anagnostidis (1998)',NULL,0,1),(183,153,'description','Unicellular - colonial; colonies free living, microscopic, sometimes elongated (up to 400 um long), in a form of an irregular or irregular-spherical net composed of mucilaginous, incidentally dividing (tube-like) strings, containing an irregular, uniserial or (later, in old colonies) multiserial and densely packed row(s) of more or less spherical, ellipsoidal, oval up to rod-like cells. Cells pale blue-green, yellowish or greyish blue, without aerotopes, sometimes forming pseudofilaments. Mucilage fine, colourless, homogeneous, sometimes visible only after staining. The mucilage envelopes the whole colony (in old colonies). In majority of species occur between or at the cells granular or ring-like, iron-oxide precipitations, usually between pairs of cells. The thylakoids are (in a small number) located<br> peripherally within the cell. Involutional filamentous cells (?).','Komárek (1992)',NULL,0,1),(184,153,'description','Zellen kugelig, zu netzförmigen Kolonien vereinigt; Netze kugelig oder flach. Maschen des Netzes in der Regel aus einer einzigen Zellreihe gebildet.','Geitler (1932)',NULL,0,1),(185,159,'description','Colonies microscopic, packet-like or subspherical-irregular, more or less rounded, with densely aggregated cells, enveloped by thin, usually firm, colourless envelopes, adjacent to cell clusters; finally in dense, sarcinoid packets, forming agglomeration of macroscopic, irregular mats. Cells spherical, subspherical, oval, hemispherical or irregular-rounded, enveloped by thin mucilaginous sheaths, usually packed closely to one another.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(186,159,'description','Unicellular- colonial; colonies microscopic, 2-l6-multicelled, sarcinoid , up to 50 um in diameter, later usually grouped into rich agglomerations of colonies, Chroococcus-like when young, later in characteristic packett-like formations with more or less cubically packed cells, enveloped usually by narrow, tight, fine or firm, colourless, sometimes slightly lamellated gelatinous envelope. Cells spherical, oval and hemispherica when young, later irregular, polygonal with rounded corners, usually densely agglomerated, flattened at the sides neighbouring to other cells; cell content blue-green or pinkish, sometimes slightly granular.','komárek (1992)',NULL,0,1),(187,163,'description','Colonies free-living, more or less spherical in outline, composed of a system of irregular and irregularly divaricate mucilaginous, indistinctly tube-like stalks radiating to all sides from the colonial center, containing short rows of rod-like cells, arranged more or less one after another; the appearance of a colony is like a densely branched bush with radially oriented branches. False branching of stalks arises after a displacement of divided cells from the original<br> direction, by the following cell division they lie in a new direction and by formation of a new sheath. Mucilaginous stalks colourless, thin, fine, sometimes diffiuent, enveloping cell rows; the slime sometimes overlaps the end cells and extends in thin threads. Cells oval to rod-shaped with rounded ends, without aerotopes.','komárek & anagnostidis (1998)',NULL,0,0),(188,163,'description','Unicellular, colonial; colourless, free floating, in outline irregularly spherical up to 55 μm in diameter, composed from irregular and irregularly branched rows of elongated cells, radiating from the centre of a colony and irregularly, densely ramified; the appearance of the colony is like the densely branched shrub with radially oriented branches. Rows of cells are enveloped by very thin, colourless and diffluent mucilage, overlapping sometimes end cells in a form of thin mucilaginous strings; wide gelatinous envelopes are missing. Cells cylindrical, rod-like with mostly cut or slightly rounded ends, straight or slightly bent, with pale green, not granular content, without prominent granules and aerotopes; end cells rounded or sometimes rounded-pointed. Common branching arise by a shift of a cell from the original position in the radial row of cells and by a folowing cell division in a new direction.','komárek (1992)',NULL,0,1),(189,167,'description','Thallus at first epilithic, more or less thick, gelatinous, forming amorphous mass with irregularly disposed cells (sometiems ensheathed), in groups or forming irregular rows of cells or pseudofilaments; later endolithic. Endolithic pseudofilaments grow parallely to one another and perpendicularly into the calcareous substrate; they are thick, enveloped by wide, distinct, clearly delimited, colourless and more or less homogeneous gelatinous envelopes. Endolithic pseudofilaments are composed of one or more rows of cells and are sometimes pseudodichotomously divaricate. Cells more or less spherical or irregular-rounaed, in epilithic parts of thallus smaller, subspherical, oval or polygonal, rarely elongate, but more spherical than in endolithic pseudofilaments, where they are usually ellipsoidal or cylindrical, clearly distant from one another. End cells sometimes wider than cells in pseudofilaments. Gelatinous envelopes in epilithic parts are usually more delimited, coloured and lamellate, than in endolithic parts, where they are colourless, more or less homogeneous. Cells pale blue-green.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(190,167,'description','Unicellular - colonial; thallus develops firstly epilithic, more or less amorphous with irregularly disposed cells, later endolithic, composed from two types of pseudofilaments in the epilithic, thick, gelatinous mass are irregular rows of cells, the endolithic pseudofilaments grow parallely into the calcareous substrate; they are thick, enveloped by wide, distinct, colourless and more or less homogeneous gelatinous envelope. Pseudofilaments are composed from one or more rows of cells and sometimes pseudodichotomously branched. Cells more or less irregular, in epilithic parts of thallus smaller, oval or polygonal, more spherical than in endolithic pseudofilaments, where they are usually more elongated, ellipsoidal or cylindrical, clearly distant one from another. End cells probably more widened, gelatinous envelopes in epilithic parts are usually more limited, coloured and lamellated. Cells pale blue-green.','komárek (1992)',NULL,0,1),(191,167,'description','Lager zum Teil epilithisch, zum Teil endolithisch, weit ausgebreitet. Aufbau aus zweierlei Fäden: epilithische Fäden auf der Oberfläche von Steinen unregelmäßig ausgebreitet, dick, endolithische Fäden senkrecht eindringend, mehr oder weniger parallel, dünn. Wachstum durch interkalare Teilungen und durch Teilung der Endzellen nach drei Raumrichtungen; Fäden in den älteren Teilen 2- oder mehrreihig, dichotom verzweigt. Zellen der epilithischen Fäden meist kugeng oder ellipsoidisch, seltener länglich, oft polygonal abgeplattet, meist Ghroococcalen-axtiig regellos verteilt und nicht deutlich fädig angeordnet; Zellen der endo-lithisehen Fäden mehr oder weniger länglich und zylindrisch, oft voneinander entfernt, oft in regelmäßigen Reihen; Endzelle der endolithischen Fäden apikal etwas verdickt. Membranen der epilithischen Fäden fest, gefärbt, oft geschichtet; Membranen der endolithischen Fäden farblos. Wahrscheinlich Gronidienbildung in den epilithischen Fäden, Nannocyten. Keine Endosporen-bildung.','geitler (1932)',NULL,0,1),(192,161,'description','Colonies microscopic to macroscopic, mucilaginous, irregular, attached to the substrate or free living, composed of several irregularly or more or less radially arranged, thick and wavy gelatinous strands, which sometimes change into an amorphous mass, particularly in basal parts of a colony; cells are placed solitary or in small groups in terminal parts of strands, very rarely In short, few-celled rows. Gelatinous strands colourless, sometimes indistinctly or distinctly transversely lamellated. Cells spherical, after division hemispherical.','komárek & anagnostidis (1998)',NULL,0,0),(193,161,'description','Unicellular - colonial; colonies gelatinous, microscopic, composed from thick, mucilaginous, colourless, more or less radially oriented and irregularly curved stalks, usually crosswise lamellated (result of one-sided production of slime from cells), at the basis confluent; stalks sometimes pseudodichotomously branched; colonies loosely joined to the substrate or free living in metaphyton or in plankton (one species). Cells disposed at the ends of stalks, enveloped their own diffluent envelopes solitary, in pairs or in irregular groups, spherical or hemispherical, rarely of irregular shape; cell content pale blue-green, olive-green or bright blue-green, usually slightly granular.','komárek (1992)',NULL,0,1),(194,161,'description','Gallertkolonien, welche aus mehr oder weniger deutlich radiär gestellten, aber unregelmäßig gekrümmten Gallertfäden zusammengesetzt sind. Zellen meist nur an den Enden, einzeln oder zu wenigen, seltener Reihen bildend, kugelig, nach der Teilung gegeneinander abgeplattet. Die Gallertfäden entstehen durch einseitige, gleichsinnige Membranbildung und Vergallertung der Membransubstanz, zeigen dementsprechend eine transversale Schichtung. Teilung der Zellen nach drei Raumrichtungen.','Geitler (1932)',NULL,0,0),(195,164,'description','Cells solitary or in twos after division (but sometimes aggregated in groups, clusters and mats), without gelatinous, envelopes or with a narrow (rarely wide), fine, hyaline, indistinct gelatinous margin around single cells. Cells widely oval to almost cylindrical with widely rounded ends, With length/width ratio = (1)1.2-1.8(2.6) : 1. Cell content with net-like (reticulate) keritomization (= irregular to radial arrangement of thylakoids, intrathylakoidal spaces). S-layer with p2 symmetry was found in <i>C. aeruginosa</i>. Net-like type of nucleoids. Involution cells irregular (never filamentous as in Synechococcus); (fig. 27d, 30). In several species motility was recorded.','komárek & anagnostidis (1998)',NULL,0,0),(196,164,'description','Unicellular; cells solitary or in irregular groups, oval, widely oval, ellipsoidal or almost cylindrical with widely rounded ends, mainly longer than 3 μm (up to 100 μm long) and (1.8)6-52 μm wide, without mucilage or with very fine and thin gelatinous layer around the cells. Cells with blue-green, olive-green or pinkish up to violet cell content, sometimes with dispersed prominent granules and with keritomized chromatoplasma (especially arranged groups of thylakpids). Cells immotile or slightly motile. GC-content of the DNA = approx. 42 mol. percent (acc. to Rippka et Cohen-Bazire 1983, only two strains studied). Involution cells irregular.','komárek (1992)',NULL,0,1),(197,170,'description','Thallous; thallus joined to the substrate, crusty, more or less of circular outline, forming circular dark reddish-black spots, which later sometimes confluent by their margins. Basal part is composed from the ˝chroococcoid˝ mass of densely agglomerated cells enveloped by their own mucilaginous, sometimes lamellated sheaths, occasionally arranged in pseudofilamentous rows, and from erected filaments repeatedly pseudodichotomously and laterally branched; branching types: V and T. Erected trichomes are uniserial, rarely two-serial. Basal cells more or less spherical or polygonal-rounded, cells in trichomes barriliform, shorter or (at the ends), longer than wide. Sheaths thin, but distinct, colourless or (when old) yellow or yellow-brown. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(198,166,'description','Filaments in fine or compact, mucilaginous mats, slightly curved or irregularly coiled, cylindrical along the whole length or slightly narrowed in the middle, without sheaths, but with very fine, colourless, homogeneous, diffluent mucilage, symmetrical, constricted at the cross walls. Cells cylindrical, more or less isodiametric or longer than wide, rarely barrel-shaped or almost spherical, without aerotopes, sometimes with dispersed granules and visible chromatoplasma, pale or bright, blue-green. Heterocytes always only terminal (arise from end cells), ovoid, oval or conical, unipored, developing at both ends of trichomes, rarely only at the one end (facultatively?). Akinetes develop only close to heterocytes, at both trichome ends, rarely spherical, usually oval or cylindrical, solitary or in rows up to 7, sometimes<br> with sculptured outer cell wall layers.','komárek (1992)',NULL,0,0),(199,162,'description','Cells occur in microscopic, free-floating colonies that are flat or platelike and composed from slightly elongated cells, the longer axis of which lies in the plane of the colony. Colonies typically are few-celled. The cells are arranged in short perpendicular rows, but have irregularities. The colony is surrounded by very fine, colorless, and diffuse mucilage. Cells are oval or ovoid, sometimes in twos or flat tetrads, have pale blue-green color and, homogeneous content. One species has gas vesicles and visible aerotopes; another species has iron precipitates within the mucilage. Cells are 1.5-5 μm long and 1-4.5 μm wide. Cells divide by binary fission in two planes in successive generations, perpendicularly to one another and to the plane of the colony.','Komárek (2003)',NULL,0,0),(200,162,'description','Colonies microscopic, free floating, flat, tabular, one-layered, few-celled, surrounded by wide, homogeneous mucilaginous envelope. Cells oval, arranged in twos or flat tetrads. Cell content homogeneous, with solitary granules. ',' Komárek & Anagnostidis (1998)',NULL,0,0),(201,162,'description','Unicellular - colonial; colonies microscopic, free living, with 1-16, mainly 4-8 cells, which are more or less regularly joined into flat, unilayered, tabular agglomerations; the short rows of cells are situated more or less perpendicularly to each other; the flat, cellular agglomerations are enveloped by the spherical, oval or ellipsoidal, not structured, fine mucilaginous envelopes; the envelopes are colour less or homogeneously coloured with fine ferric precipitations. Cells more or less oval, ellipsoidal or slightly irregular ovoid, usually tightly joined one to another; colonies usually slightly elongated in the direction of the longer axis of cells. Cell content pale blue-green or olive green, without aerotopes, sometimes with dispersed granules.','Komárek (1992)',NULL,0,1),(202,169,'description','Cells solitary or aggregated into groups, polarized, attached by one end to the substrate (by narrower,almost stalk-like, or widened, flattened basal part), hemispherical, oval or club-shaped, with thin or thick, sometimes lamellate, colourless sheaths.','komárek & anagnostidis (1998)',NULL,0,0),(203,169,'description','Solitary cells or groups of cells, ,joined to the substrate. Cells more or less polarized, attached to the substrate by the gelatinous pad and by rounded basis; apical end +/- rounded; they are vase-like or club-shaped, narrowed or widened to the basis. Around cells firm, sometimes lamellated sheaths, which are later ˝opened˝ at the apical end (pseudovaginae). Cell content greyish blue-green, olive-green or pinkish red, finely granular, always without aerotopes.','komárek (1992)',NULL,0,0),(204,171,'description','Filamentous - thallous; filaments heteropolar, differentiated into basal and apical parts, obligatory commonly falsely branched, solitary or in fasciculated colonies or strata; false branching lateral, always with only one branch, growing usually at first parallely with original trichome, later diverging. Trichomes and branches with basal heterocytes, rarely develop intercalar heterocytes, solitary or (rarely) in twos; heterocytes usually heteropolar (unipored). Sheaths always present, usually firm, colourless or yellow-brown and lamellated, at the end joined to the trichome or widened and diverging. Trichomes with cylindrical or barrel-shaped cells, at the cross walls constricted or unconstricted, hair-like narrowed to the apical ends; hairs are composed from a row of long, narrow, hyaline cells. Aerotopes and akinetes lacking.','komárek (1992)',NULL,0,0),(205,172,'description','Main generic diacritical characters (obligatory for all species):<br> - The genus Dolichospermum (evaluated by 16S rRNA gene sequencing) belongs genetically into the unique cluster of nostocalean heterocytous cyanobacteria.<br> - This genetically separated group (Dolichospermum) represents a complex cluster, the different members of which do not differ less than in 92% of 16S<br> rRNA gene similarity one from another.<br> - Trichomes are isopolar, metameric with respect to heterocytes position, with constrictions at cross-walls, without firm sheaths, sometimes with fine<br> mucilaginous, diffluent envelopes. The growth of trichomes is theoretically endless.<br> - Apical cells are morphologically similar to vegetative cells, they are not differentiated and are able to divide.<br> - Gas vesicles occur obligatorily in cells in vegetative phase. They are joined into irregular aerotopes (sooner “gas vesicles”) over the whole cell volume;<br> aerotopes are recognizable in cells under optical microscope.<br> - Heterocytes arise intercalarly, solitary (exceptionally in pairs); they develop from vegetative cells in ± metameric position.<br> - Akinetes develop paraheterocytically, it means connected with heterocytes, rarely aside heterocytes from both sides or (more commonly) separated from them<br> by several cells, solitary up to 5(6) in a row. They develop successively in the direction from heterocytes and often arise after fusion of two or few neighbouring vegetative cells. The ripe akinetes are usually three or more-times larger than vegetative cells.<br> - All species (morphotypes) are planktic in vegetative state, never form sessile mats on the substrate. The filaments live solitary or in small clusters.<br> Autapomorphic characteristics: Filaments living isolated or in free clusters; metameric structure of trichomes with heterocytes developing solitary;<br> obligatory gas vesicles in vegetative cells; akinetes develop paraheterocytically.','wacklin et al. (2009)',NULL,0,0),(206,177,'description','Colonial; thallus epilithic, small, pulverous, thin, irregular, composed from basal Gloeocapsa-like agglomerations of more or less spherical or hemispherical cells and radiating pseudofilamentous, short rows of cells, enveloped by common sheath; rows of cells grow all-sided, paralle1y and densely arranged and irregularly ˝branched˝. Sheaths more or less thickened, open at the apex of pseudofilaments; around cells usually own mucilaginous sheaths. Cells in pseudofilaments more or less oval, irregularly elongated or almost cylindrical.','komárek (1992)',NULL,0,0),(207,174,'description','Colonies mucilaginous, microscopic to macroscopic, more or less spherical, oval or ovoid, sometimes formed from hemispherical subcolonies, up to 1 cm in diameter, with distinct and delimited, firm pellicular surface. Cells almost spherical or oval up to long cylindrical, without their own gelatinous envelopes, in young colonies irregularly distributed, later in more or less regular, parallel and radially oriented rows, surrounded by scarcely visible (staming !) tube-like gelatinous sheaths.','Komárek & Anagnostidis 1998',NULL,0,0),(208,174,'description','Unicellular - colonial; colonies spherical or oval, later irregular, macroscopic, up to 1 cm in diameter (later more), sometimes composed from subcolonies, limited by firm mucilaginous layer (˝periderm˝); daughter colonies connected sometimes with the original mother colony by gelatinous, hyaline, wide strings, which later disappear. Cells spherical up to oval or shortly rod-like, particularly before division elongated or up to several times longer than wide (involution forms ?), within colony disposed in radial rows and sometimes in gelatinous tubes, which are, however, situated irregularly inside of colony.',' Komárek (1992)',NULL,0,1),(209,179,'description','Colonies free-living, usually in metaphyton or rarely on soil, cubic, with cells, arranged three-dimensionally in perpendicular rows; sometimes large colonies composed of sub- colonies; colonies small, few-celled or ,multicellular with up to more than 128 cells; rows mold colonies sometimes a little disturbed. Mucilage colourless, hyaline, delimited, rarely diffluent (sometimes almost invisible); special gelatinous envelopes around cells are absent or indistinct, facultative. Cells spherical or widely oval before division.','komárek & anagnostidis (1998)',NULL,0,0),(210,179,'description','Unicellular - colonial; colonies microscopic, more or less cubic (three-dimensional) up to irregular, mucilaginous, sometimes agglomerated in groups of colonies, free living in metaphyton or in soil, enveloped by colourless, usually diffluent or limited mucilage; cells are arranged into perpendicular rows, later sometimes slightly irregular. Cells spherical or slightly elongated (before division), situated tightly or more or less distant one from another, without aerotopes, pale greyish blue-green or bright blue-green, mainly with slightly granular content. Mucilaginous envelopes unstructured or slightly concentrically lamellated, keeping more or less the cubic form of a colony. The facultative motility of cells in cultures was described in the ˝High GC-cluster of Synechocystis˝ (Waterbury 1989) belonging probably to this genus.','komárek (1992)',NULL,0,0),(211,179,'description','Zellen kugelig, durch regelmäßig abwechselnde Teilungen nach drei Raumrichtungen in geraden Reihen angeordnet und zu Würfeln oder Quadern vereinigt, manchmal in  Vierergruppen, meist ohne deutliche Spezialhüllen, in gemeinsamer Gallerte. Kolonien freischwimmend.','geitler (1932)',NULL,0,0),(212,178,'description','Thallus epilithic, in the form of small, microscopic, slightly globular or formless colonies, consisting of basal groups of irregular-rounded, ellipsoidal or pear- shaped cells, which are irregularly arranged and mainly enveloped by stratified sheaths (gloeocapsoid stages); later very short, only few-celled pseudofliaments are formed, which grow parallel to one another and vertically from basal clusters, and are pseudodichotomously or pseudotetrachotomously diversified;<br> sheaths around cells within pseudofliaments, or enveloping also the whole row of cells (pseudofilaments), sometimes stratified.','komárek & anagnostidis (1998)',NULL,0,0),(213,173,'description','Filamentous – thallous; filaments attached to the substrate, erected, joined to the fasciculated, brownish thallus, up to 1/2 cm long, but without special adhering cellular organelles or discs. Trichomes uniserial, laterally (usually unilaterally) true-branched (T-type), composed from barrel-shaped cells, Basal parts of filaments thick, torulous, not branched, younger parts thinner, more or less cylindrical, morphologically different from basal filaments; in upper parts of filaments common ramification, branches short, arcuated. Sheaths thin or thick, colourless up to yellow-brown, sometimes copying the moniliform shape of trichomes; around cells in old filaments own thick envelopes. Cells with homogeneous or granular (often peripherally) content, more or less isodiametrical, old cells sometimes vacuolized, cells in hormogonia granular. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(214,176,'description','Colonies are microscopic to (rarely, when old) macroscopic, composed of clusters of irregular mucilaginous spheres or elongated formations, with smooth surfaces, on which scarce and irregularly situated solitary cells are observed (from above). Mucilage is firm, homogeneous, colorless, and distinctly delimited. Cells are widely oval to cylindrical, up to 4.2 μm long, distant (after division in pairs), with no obvious gas vesicles, and pale blue-green. Cell division is only in one plane in successive generations, perpendicular to the longer cell axis.','Komárek (2003)',NULL,0,0),(215,176,'description','Colonies mucilaginous, more or less spherical, oval or elongate, microscopic, solitary, in pairs or compound, forming irregular groups where colonies of different size are tightly grouped together, free floating in the plankton, metaphyton, or living in sapropel; cells distributed irregularly and distant from each other on the surface of the primary colonial mucilage (hyaline gelatinous spheres or cylinders), without their own gelatinous envelopes. Mucilage of primary colonies homogeneous, delimited, smooth on the surface. Cells oval or rod-shaped, small, short, without aerotopes or prominent granules. ',' Komárek & Anagnostidis (1998)',NULL,0,1),(216,176,'description','Unicellular - colonial; colonies microscopic in a form of slightly irregular mucilaginous spheres, on the surface of which are scarcely, irregularly distributed elongated cells; gelatinous spheres composed usually into irregular agglomerations. Mucilage homogeneous, not structured, colourless, limited with more or less firm margin. Cells oval or rod-like, more or less distant one from another, without aerotopes, pale blue-green or greyish.',' Komárek (1992)',NULL,0,1),(217,182,'description','Filamentous; filaments heteropolar, differentiated into basal part with a heterocyte and free apical end, cylindrical, simple, solitary or in small groups; filaments usually creeping on the substrate or growing in periphyton. Sheaths_firm, envelop always only one trichome, colourless, sometimes thick and lengthwise and crosswise layered. Trichomes always with a basal, hemispherical or spherical heterocyte rarely also with cylindrical intecalar heterocytes, at which trichomes disintegrate; trichomes cylindrical or slightly widened at the base, narrowed in the middle part and clearly widened at the ends, constricted or unconstricted at the cross walls, but usually constricted at the ends. Cells cylindrical or barrel-shaped, in the middle part usually clearly longer than wide, at the bases and at the ends shortened up to isodiametrical or shorter than wide; end cells widely rounded or spherical. Aerotopes absent. Akinetes develop rarely in basal parts of trichomes, usually in rows and separated by heterocytes (known in several species only).','komárek (1992)',NULL,0,0),(218,185,'description','Heteropolar cells joined to the substrate by one end, solitary or in irregularly parallel or stellate groups. Cells ovoid-oval or shortly club-shaped when young, later cylindrical, rod-shaped, rounded at the apex, slightly and shortly attenuate or rounded at the base, attached to the substrate by fine mucilaginous pad, scarcely visible in light microscope (staining !); without sheaths. Cell content homogeneous, grey-blue, blue-green or olive-green, rarely. slightly granulate, sometimeswith differentiated chromato- and centroplasmic areas (peripheral arrangement of thylakoids).','komárek & anagnostidis (1998)',NULL,0,0),(219,185,'description','Solitary cells or groups of cells, joined by one end to the substrate. Cell polarized, differentiated in the rounded and sometimes narrowed basal end, attached by the help of a small mucilaginous pad to the substrate (staining !), and in the apical rounded end; they are cylindrical, straight or slightly curved, slightly club-shaped or oval when young, without any sheath. Cell content greyish or pale blue-green, more or less homogeneous or slightly granular. Thylakoids situated peripherally along the cell walls as a visible chromatoplasma. Filamentous involution cells.','Komárek (1992)',NULL,0,0),(220,183,'description','Filamentous; filaments heteropolar with firm, common, lamellated, at the ends open and lacerated sheaths, up to 300 μm in diameter at the basis (in the upper part narrower), enveloping many parallely, fuscicle-like oriented (coaxial) trichomes with their own lamellated sheaths, up to 1 cm high; filaments repeatedly (up to 5-times) falsely branched, divaricated or forming the compact blue-green strata on the substrate; the upper part of filaments and their branches usually slightly swollen, where are the meristematic zones of trichomes. Common sheaths thick, hyaline, in the inner portions usually yellowish-brown. Trichomes blue-green, heteropolar, with a basal heterocyte, usually a little widened at the basis, later thin and again clearly widened in the upper part, at the ends narrowed and sometimes elongated into short or long hairs; commonly are developed intercalar heterocytes, at which trichomes disintegrate (false branching) and develop their own sheaths; trichomes in the middle, narrow part more or less cylindrical,<br> not constricted at the cross walls, at bases and in upper widened parts sometimes constricted. Cells blue-green, at bases shorter or slightly longer than wide, in the middle (narrow) part cylindrical and usually longer than wide, in the upper parts shorter than wide and again elongated in hyaline hairs. Heterocytes of different form, hemispherical, spherical, oval up to long cylindrical. Aerotopes and akinetes unknown.','komárek (1992)',NULL,0,0),(221,181,'description','Filamentous - thallous; filaments single or in fascicles, arranged parallel or coiled within a common gelatinous, diffluent mass, enveloped by their own, fine sheaths, with common, lateral true-branchings (T-type), uniserial, rarely multiserial, with club-shaped ends of trichomes and branches. Branches arise after the lengthwise cell division in main trichomes, sometimes very commonly; they are long or short (in the latter case they change completely in hormogonia), with diffluent, fine sheaths. Trichomes usually constricted at cross-walls, with barrel-shaped cells, isodiametric or shorter or longer than wide. Occasionally occurs false branching. Heterocytes solitary in main filaments and in long branches, short. Akinetes develop solitary, rarely, in main creeping trichomes, subspherical.','komárek (1992)',NULL,0,0),(222,180,'description','Filamentous - thallous; thallus usually felt-like, rarely in compact mats, composed from creeping, uni- or multiserial filaments and morphologically different, more or less erected uniserial branches. Creeping trichomes usually moniliform, enveloped by thick, waved, sometimes slightly lamellated and coloured sheath, with usually barriliform cells, sometimes enveloped by their own gelatinous sheaths; erected true branches develop usually unilaterally after the lengthwise cell division in basal trichomes (T-type of branching), usually cylindrical, with cylindrical and often elongated cells and thin, mainly colourless sheaths. Cells usually with slightly granular<br> plasma, thylakoids distributed irregularly over the whole cell content. Heterocytes intercalar, subspherical in basal trichomes, cylindrical in branches. Akinetes develop occasionally and irregularly in basal trichomes (known only in few species).','komárek (1992)',NULL,0,0),(223,184,'description','Filamentous - thallous; thallus loosely tufted, up to 2 mm thick, with coiled, creeping or erected filliments, irregularly laterally and pseudodichotomously true branched (V- and T-branching types), without prostrate basal system and without morphological differentiation into main and lateral branches. Sheaths firm, intensely lime-incrusted, colourless , containig a single trichome. Trichomes uniserial, moniliform, indistinctly or intensely constricted at cross-walls.<br> Cells cylindrical or barrel-shaped, sometimes with own, narrow special envelopes and granular, pale greyish-green content, with distinct chromatoplasma and solitary granules; end cells sometimes slightly widened-rounded. Thylakoids distributed over the whole cell content. Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(224,189,'description','Cells solitary or aggregated in irregular groups, widely oval or rod shaped, surrounded by narrow, delimited gelatinous envelopes, containing one or more ensheathed cells. Cells non motile.','komárek & anagnostidis (1998)',NULL,0,1),(225,189,'description','Unicellular; cells solitary or in irregular groups, rod- shaped or widely oval up to almost spherical, with thin, fine and indistinct or multilayered sheaths around the cells and helding sometimes more cells together. Immotile. Cells with almost colour less content and solitary granules, in masses violet. Thylakoids and phycobilisomes absent, a cytoplasmatic membrane, which follows the contour of the cell wall, is the only unit membrane system in the cell. GC-content of the DNA = approx. 65 mol. percent. Without involution cells.','komárek (1992)',NULL,0,1),(226,187,'description','Cells cyanoprokaryotic, solitary, spherical or slightly oval, after division hemispherical and for a short time two (four) together, never forming colonies, 3-10 um in diameter, without mucilage or (mainly) with narrow, fine, colorless, and usually diffluent and indistinct mucilaginous envelopes. Cell content homogeneous, without separation of centroand chromatoplasma, sometimes with lengthwise striation (thylakoids situated in cells lengthwise). Color of cells is pale blue-green, bright-green, grey, or pinkish.','Korelusová et al. (2009)',NULL,0,0),(227,186,'description','Filamentous; filaments unbranched, rarely solitary, usually more or less parallely oriented in fine, smooth, diffluent and membranaceous mats, microscopic and later macroscopic, covering the substrate; trichomes always without sheaths, isopolar, straight or slightly waved or coiled, narrow, more or less thin, 1-4 um wide, uniserial, composed of cylindrical cells, slightly constricted or unconstricted at the cross walls, usually narrowed and slightly bent to the ends, usually intensely motile. Cells cylindrical, elongated, more or less isodiametrical (rarely), later always longer than wide (up to several times). without aerotopes, sometimes with several prominent granules (carotenoids), with thylakoids arranged concentrically along the cell walls; end cells rounded or (usually) narrowed and bent, sometimes hooked, pointed or narrowed-rounded, sometimes terminated by spherical calyptra. Cell content pale blue-green, yellowish green, olive-green or bright green, without chromatic changes (?). Heterocytes and akinetes absent.','komárek (1992)',NULL,0,1),(228,175,'description','Colonies gelatinous, irregular, granular, microscopic to macroscopic and covering the substrate, sometimes (especially when young) polarized, attached to the substrate, later composed of subcolonies forming aggregates, which are sometimes radially or serially disposed within the thallus. Cells or their groups disposed in colonies more or less in radial or erect rows, enveloped by their own, usually layered and distinct,. delimited mucilaginous envelopes; cells spherical to irregular, often of variable size in a colony, with pale blue-green, olive-green or  yellowish, finely granular content.','komárek & anagnostidis (1998)',NULL,0,0),(229,175,'description','Unicellular - colonial; colonies gelatinous, irregular, granular, microscopic up to macroscopic and covering the substrate, composed from agglomerated subcolonies, which are sometimes radially disposed within the thallus. Cells or their groups disposed in colonies more or less in radial or erected rows, enveloped by their own, usually layered mucilaginous envelopes; cells spherical up to irregular, in one colony often of different size, with pale blue-green, olive-green or yellowish, finely granular content.','komárek (1992)',NULL,0,1),(230,175,'description','Zellen mit weiten, blasigen, ineinandergeschachtelten Membranhüllen; Zellen bzw. Zellgruppen in aufrechten Reihen angeordnet, weit ausgebreitete, krustige Lager bildend. Dauerzellen.','geitler (1932)',NULL,0,0),(231,188,'description','Filamentous; filaments (trichomes) solitary, thin (up to 3 μm wide), without sheaths, regularly screw-like coiled with wide and more or less long screws, usually intensely motile (rotation). Sometimes slightly flexible, cylindrical, not attenuated to the ends, not constricted at the cross walls. Cells pale blue-green or yellowish, with homogeneous content, sometimes with few fine granules, probably always longer than wide.','komárek (1992)',NULL,0,0),(232,192,'description','Colonies usually small, composed of sheathed cells or groups of cells (2-, 4- or more-celled); cells obligatorily enclosed within their own gelatinous envelopes and sometimes surrounded by common mucilage, usually in and irregularly distributed in large agglomerations (micro- to macroscopic mucilaginous or «granular˝ thallus). Cells and groups of cells enclosed in hyaline or concentrically lamellate, colourless or intensely bluish, violet or yellow-brown envelopes, delimited at the margin. Cells widely oval to rod-shaped, rounded at the ends, pale blue-green, blue-green, olive-green or violet.','komárek & anagnostidis (1998)',NULL,0,1),(233,192,'description','Unicellular - colonial; colonies (groups of cells) microscopic or forming multicellular agglomerations of small colonies, up to macroscopic, gelatinous, granular or in amorph layers; cells or their groups enveloped always by own mucilaginous, usually concentrically lamellated, limited envelopes, which copy the cell form. The mucilage layers are developed by the periodical production of slime from cells; mucilage colourless, yellow-brownish, bluish or dark blue, rarely reddish; cells situated in colonies irregularly, more or less distant one from another. Cells widely oval, oval or rod-like, pale greyish blue, blue-green or olive green, usually with slightly granular content or with several prominent granules.','komárek (1992)',NULL,0,1),(234,192,'description','Zellen ellipsoidisch bis zylindrisch, gerade oder gebogen, an den Enden nicht verjüngt oder zugespitzt, sondern breit abgerundet, in kleinen Kolonien oder großen Lagern. Teilung senkrecht auf die Längsachse, Verteilung der Tochterzellen nach drei Raumrichtungen. Hüllen- und Koloniebau in den typischen Fällen nach Art von Gloeocapsa: Hüllen blasig, ineinandergeschachtelt, geschichtet oder ungeschichtet; manchmal die äußeren Hüllen verquellend, die Zellen dann nur von Spezialhüllen umgeben und in gemeinsamer Gallerte eingebettet. Hüllen farblos oder gelb bis braun, blau bis violett (oder rot ?) gefärbt. Nannocytenbildung in typischer Weise (unter starker Verkleinerung der Zellen) anscheinend selten, oft aber angedeutet durch schnellen Teilungsablauf, wodurch mehrere kurze bis fast kugelige Zellen ohne Spezialhüllen in einer gemeinsamen Hülle zu liegen kommen. Dauerzellen unbekannt.','geitler (1932)',NULL,0,1),(235,191,'description','Rarely solitary cells, mostly micro- or macroscopic, irregular, formless or granular colonies, composed of densely, irregularly aggregated cells or their small goups, surrounded by mucilaginous envelopes. Cells subspherical, more or less irregular-rounded in outline, sometimes slightly elongate (never spherical), enveloped by thin, narrow, clearly delimited, rarely slightly diffluent, sometimes feebly lamellate, often coloured sheaths (yellow, red, rusty red, etc.), usually following the cell outline.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(236,191,'description','Unicellular- colonial; colonies microscopic, later agglomerated into macroscopic, disintegrating granular, irregular strata, subaerophytic or submerse, mainly on stony substrates. Cells more or less spherical, later irregular, rounded polyedrical, agglomerated into irregular packets, differently large, with own mucilaginous, limited, firm, lamellated or not lamellated and colou- red, usually not very wide envelopes which sometimes more or less copy the cell shape; groups of cells unified together by the common mucilaginous sheath. Cells with blue-green, usually homogeneous content. Sheaths coloured, yellow- brown or orange-reddish up to violet.','komárek (1992)',NULL,0,0),(237,190,'description','Colonies micro-, later macroscopic (rarely only microscopic), usually multicellular, mucilaginous, amorphous, epilithic or epiphytic (rarely free floating or metaphytic), composed of small groups of irregularly arranged cells, enveloped by wide, usually stratified individual gelatinous envelopes, joined together into a formless mass. Cells and their groups always surrounded by wide gelatinous sheaths, concentrically lamellate (lamellation distinct or scarcely visible), in several species intensely or partly coloured by sheath pigments (gloeocapsin, scytonemin), yellow, yellow-brown, orange, red, blue or violet; gelatinous envelopes do not copy exactly the cell shape. Gelatinous envelopes usually delimited, only in some stages of the life cycle or under special conditions diffluent (also sometimes in cultures). Cells always spherical or rarely indistinctly elongated and oval, after division hemispherical, usually with pale blue-green, homogeneous content, sometimes with solitary granules; gas vesicles only in one planktic species.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(238,190,'description','Unicellular - colonial; colonies microscopic, small in a form of irregular agglomerations, or large, up to macroscopic, gelatinous, amorph, sometimes covering large areas of wet stony substrates; colonies composed from groups of cells, which are closed in mucilaginous, usually wide and concentrically lamellated envelopes, in several species intensely reddish, bluish, orange or yellowish coloured; cells situated in colonies irregularly, more or less distant one from another, in old colonies in great numbers. Mucilaginous envelopes fine, but layered and limited; solitary cells produce soon after division their own, wide envelopes, which do not just copy the cell shape. Cells spherical, only shortly after division hemispherical, pale blue-green or olive-green, usually with slightly granular content. During vegetation cycles develop mor- phologically different stages (status), conditioned by ecological influences.','komárek (1992)',NULL,0,1),(239,190,'description','Zellen kugelig, zu 2 - 8, seltener zu mehreren in Kolonien, mit ineinander geschachtelten, blasig aufgetriebenen Membranhüllen. Kolonien einzeln oder zu vielen beisammen und dann oft weitausgedehnte Lager bildend. Membranhüllen geschichtet oder ungeschichtet.<br> Zellteilungen meist regelmäßig abwechselnd nach drei aufeinander senkrecht stehenden Raumrichtungen; Zellen in größeren Kolonien oft sekundär verschoben und infolge ungleichzeitiger Teilungen unregelmäßig gelagert. Gelegentlich Nannocytenbildung, häufig Aphanocapsa-artige Stadien. Bei einigen Arten große Zellen mit fester Membran (Dauerzellen); Dauerzellen oft infolge von Umwandlung eben geteilter Zellen zweiteilig.','geitler (1932)',NULL,0,1),(240,198,'description','Filamentous - thallous; thallus crusty, flat, 2-3~layered, widely spread on the substrate, with usually erected, parallely and densely arranged or slightly tangled filaments, confluent laterally by their sheaths. Trichomes uniserial, rarely with two cells aside, with constrictions at cross-walls, cylindrical or slightly narrowed in the basal and widened near the apical part; in the upper parts with numerous false branchings, in the lower ones with true branchings of the T-type; branches arising from false ramification are usually short, perpendicular to the original trichome, changing often into hormocysts. The lower parts of thallus with destroyed, dying trichomes. The true branches grow initially perpendicularly to the mother trichome, later curve to the direction of the original trichome. Sheaths around old trichomes usually colourless, homogeneous and thin, diffluent and confluent at the margin, in the younger (upper) part of thallus lamellated, funnel-like striated, with yellow- brown inner layers. Cells barrel-shaped. Heterocytes intercalar or basal (after false branching), solitary. Akinetes not known.','komárek (1992)',NULL,0,0),(241,195,'description','Colonies are free-living, spherical or irregularly oval, and sometimes composed of subcolonies. They have a central system of thick mucilaginous stalks that are nearly pseudodichotomously divided and may be diffuse within the colony. Stalks widen at the ends and envelope individual cells with a thin mucilage layer. Cells are slightly elongate, obovate, or club-shaped, and radially oriented more or less at the colony periphery, which is sometimes enveloped by a fine, colorless, and diffuse mucilage. Cells have a homogeneous pale or bright blue-green, olive-green, or red content and are (4.2)6-12(15) X 2-8(13.2) μm. After division, the cells may remain joined together and form a characteristic cordiform shape. Cells in colonies are slightly distant and sometimes slightly radially displaced from one another. Cell division occurs in two planes in successive generations, perpendicular to one another and to the colony surface. Reproduction is by colony disintegration','Komárek (2003)',NULL,0,0),(242,195,'description','Colonies spherical or irregular, commonly composed of subcolonies, free-living, sometimes enveloped by indistinct, fine and diffluent mucilage; from the center of colony radiates a system of more or less thick, gelatinous stalks, which are, however, always thinner than the cell width; stalks are widened at the ends and envelope individual cells with a narrow layer; the stalk system is sometimes diffluent in the middle of the colony. Cells are always elongate, radially situated at the ends of stalks, obovate or club-shaped, after division remain and grow parallely joined together for a long part of the cell cycle, forming the characteristic cordiform shape. Solitary cells or cordiform couples are always slightly distant from one another with remarkable spaces between them, sometimes slightly radially displaced from one another.','Komárek & Anagnostidis (1998)',NULL,0,0),(243,195,'description','Unicellular - colonial; colonies microscopic, spherical or irregular, commonly composed of several daughter colonies, free living (mainly in the metaphyton), usually enveloped by narrow, indistinct, fine and diffluent mucilage. A system of +/- thick, pseudodichotomously branched and radially oriented stalks widened to the ends and envelopin the individual cells by a narrow layer of slime sometimes visible only after staining (!) is developed within the colony; the stalk system is (sometimes<br> diffluent in the colonial center. Cells radially oriented, situated in the periphery of a colony, always elongated, obovate or club-shaped, after division remain and grow joined (by their longer sides) together for a long part of the cell cycle, forming the characteristic cordiform shape; solitary cells or ˝cordiform˝ stages are always slightly distant one from another with remarcable spaces between them, usually slightly radially shifted to one another. Cells pale blue-green, yellowish or pinkish, without aerotopes, sometimes<br> with solitary granules, in colonies situated more or less peripherally and radially.','Komárek (1992)',NULL,0,1),(244,195,'description','Zellen ellipsoidisch, verkehrt-eiförmig oder abgerundet kegelig, während der Teilung herzförmig, seltener fast kugelig, oft in Vierergruppen, mit oder ohne Spezialhülle, in einer Schicht in gemeinsamer Gallerte zu hohlkugeligen, freischwimmenden Kolonien vereinigt, auf radiär gestellten, verzweigten Gallertstielen sitzend. Zellteilung meist nach zwei aufeinander senkrecht stehenden Raumrichtungen. Gelegentlich Teilung der ganzen Kolonie.','Geitler (1932)',NULL,0,1),(245,193,'description','Filamentous - colonial; trichomes heteropolar with basal heterocytes and apical hair-like ends with own sheaths, united radially into gelatinous, hemispherical or spherical colonies, which are microscopic up to several cm in diameter, olive green, yellow-green, brown or dark blue-blackish. The whole colony enveloped by a fine or firm slime; trichomes always oriented with heterocytes in to the centre of the colony. Trichomes rarely false branched (during trichome division), the branches separate soon from the mother trichome, but remain parallel and radially located within the colonial slime and form their own gelatinous sheaths. Colonies are joined to the substrate or free floating. Trichomes uniserial, rarely with intercalar heterocytes (developing before or during trichome disintegration), constricted or unconstricted at the cross walls, more or less straight or coiled. Sheaths are always present, but sometimes gelatinize within the mucilage of colonies, especially near apicall parts of trichomes (near the margin of a colony). Upon the basal heterocytes oval or cylindrical akinetes develop (solitary or in rows) at the end of the vegetation periods. The cells in several species (particularly in hormogonia) contain aerotopes (planktic species).','komárek (1992)',NULL,0,0),(246,194,'description','Filamentous; filaments (trichomes) solitary, uniserial, without sheaths, straight, short, flattened from sides and composed from C-like curved cells forming a tube-like formation with a norrow or wide opening along the whole trichome length, which can be localized straight or slightly screw-like on the trichome; cross walls slightly constricted or unconstricted, trichome ends not attenuated or slightly narrowed. Cells very short, flattened and curved, at the cross section in the form of ˝C˝. Heterocytes and akinetes lacking.','komárek (1992)',NULL,0,0),(247,201,'description','Filamentous - thallous; thallus (mats) composed from clusters of irregularly coiled, true-branched filaments; trichomes uniserial, morphologically not diversified in main trichomes and branches, constricted at cross-walls, with typical reverse Y-branchings, more or less cylindrical, not attenuated to the ends, with rounded end cells, enveloped by thick sheaths. Sheaths firm, widened, lamelated, yellow-brown, sometimes with hyaline outer layers. Cells cylindrical or barrel-shaped. Heterocytes intercalar, elongated, cylindrical or barrel-shaped. Akinetes not known.','komárek (1992)',NULL,0,0),(248,200,'description','Filamentous; filaments heteropolar, with basal parts with heterocytes and free apical ends, commonly falsely branched with solitary lateral branches initiating at the heterocytes (mainly unipored) and fragile (sometimes liberating from the “mother” filament), united in fasciculate, caespitose, crustaceous, thin or woolly mats, sometimes creeping on a substrate; branches diverging from the main trichome, more or less short, usually arcuated. Sheaths thick, firm, lamellated, colourless or yellow-brown, open at the apex. Trichomes and branches with basal (rarely also with intercalar) heterocytes, cylindrical, not attenuated or slightly attenuated at apexes, constricted at the cross walls. Cells barrel-shaped, shorter than wide up to discoid; end cells slightly narrowed and widely rounded, with granular content. Aerotopes and akinetes lacking. Cells divide crosswise to the trichome axis, characteristic are the &nbsp;terminal meristematic zones. Reproduction by separated branches or &nbsp;hormogonia, which germinate at both sides, but later (after formation of &nbsp;heterocytes); they change in heteropolar growth.','Komárek (1992)',NULL,0,0),(249,199,'description','Filamentous - thallous; thallus from free, coiled filamentous clusters, joined to the substrate, later sometimes free floating in metaphyton. Filaments irregularly arcuated, with uniserial trichomes (only rarely with some cells length-wise divided), laterally (usually unilaterally) true-branched (T-type) and morphologically not differentiated in main and lateral trichomes, only rarely are branches slightly narrower. Sheaths thin, colourless, rarely indistinctly layered. Heterocytes intercalar, exceptionally lateral. Cells cylindrical, only rarely indistinctly constricted at cross-walls or barrel-shaped, sometimes with finely and sparsely<br> granular content. Heterocytes intercalar, cylindrical. Sometimes occur solitary akinetes.','komárek (1992)',NULL,0,0),(250,203,'description','Filamentous; filaments solitary or in_groups, heteropolar, joined with one end to the substrate (usually by a pad or a short leg) and with free second end, with simple, firm, colourless, thin sheath enveloping the trichome and open at the apex. Trichomes thin, mainly up to 4 μm wide, uniserial, simple, +/- straight (˝starr˝), curved or slightly flexuous, not attenuated at the ends, constricted or unconstricted at the cross walls. Very rarely false branching with one lateral branch, after division of trichomes between two vegetative cells. Cells shorter up to longer than wide, cylindrical or barrel-shaped; end cells rounded or conically rounded, without aerotopes. Heterocytes and akinetes lacking.','komárek (1992)',NULL,0,0),(251,202,'description','Thallous; thallus in form of small, simple, three-dimensional, tetrahedral, cubic or iregular, packet-like clusters of densely and irregularly gathered cells of indefinite size, microscopic; cells sometimes arranged in short rows, without enveloping common mucilage. Cells irregular, subspherical, flattened at sides connected with neighbouring cells, with blue-green, slightly granular content. Around cells firm, thin, not gelatinizing and not stratified colourless sheaths. Heterocytes subspherical or hemispherical, developing at sides (marginally) of cell clusters. Akinetes not observed.','komárek (1992)',NULL,0,0),(252,204,'description','Thallous; thallus composed from haevily pseudodichotomously ramified, heteropomr, more or less creeping fimments. Trichomes uniserial, torulous, with numerous short true branches, not morphologically diversified from main trichomes (V- and T- type of branching); sheaths firm, thin, limited, waved at the surface, colourless, not lamellated, not gelatinizing, only at the end (around hormogonia) slightly lamellated and telescopic; trichomes and branches from dense agglomerations, but not confluent by sheath sides. Cells irregularly subspherical or barrel-shaped, connected in trichomes by pit-connections. Heterocytes and akinetes not observed.','komárek (1992)',NULL,0,0),(253,113,'description','Filamentous - thallic; filaments solitary, in fascicle-like colonies or in mats (microscopic up to macroscopic), composed from (1)2 to several trichomes closed within the firm or more or less mucilaginous, usually slightly widened, colourless, sometimes slightly lengthwise (and rarely also crosswise) lamellated, or outer diffluent sheaths, open at the apex; the filaments are isopolar or more or less polarized (not trichomes!), sometimes specifically branched, but without typical tolypotrichoid or scytonematoid false branching (sheaths are branched only, never trichomes). Trichomes 8-30μm wide, long, uniserial, more or less flexuous or waved, isopolar, composed from shortly cy1lndrical cells, slightly constricted or unconstricted at the cross walls, not attenuated towards ends. Cells always several times shorter than wide (discoid), without aerotopes, usually with fine granulation; end cells widely rounded, sometimes with a narrow calyptra. Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(254,206,'description','Thallus mainly epilithic, with irregularly or +/- in rows clustered cells, or pseudofilamentous. Epilithic pseudofuaments are composed of the irregular uni- or multiseriate rows of irregular groups of more or less spherical cells, which are surrounded by their own mucilaginous, sometimes widened and slightly lamellate envelopes; sometimes develop endolithic (boring) pseudofilaments, which grow directly into the limestone substrate and are composed of uniseriate rows of cells which are usually distant from one another, and separated by thick, mucilaginous, usually transversely lamellate and layered sheaths; all pseudofilaments are enveloped by lamellate, gelatinous, wide and delimited sheaths, sometimes coloured, yellowish-brown or violet, sometimes laterally (or pseudodichotomously) divaricate («branched»). «Branches» are lateral and arise after the lengthwise division of cells in pseudofllaments; endolithic pseudofllaments sometimes consisting only of one (-2) terminal cells. Cells spherical, irregular or polygonal, slightly elongate in euendolithic pseudofilaments, usually wider at their ends.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(255,206,'description','Unicellular - colonial; thallus composed from epilithic and endolithic pseudofilaments. Epilithic pseudo filaments form the irregular uni- or mor~ seriate rows or irregular groups of more or less spherical cells, which are enveloped by their own mucilaginous, sometimes widened and slightly lamellated envelopes; endolithic (boring) pseudofilaments grow directly into the limestone substrate and are composed from uniseriate rows of cells which are distant one from another, separated by thick, mucilaginous, usually crosswise lamellated layers; all pseudofilaments are enveloped by lamellated gelatinous, wide sheaths, sometimes coloured, yellowish-brown or violet, sometimes divaricated (˝branched˝). Cells spherical, irregular or polygonal, slightly elongated in endolithic pseudofilaments, usually more widened at their ends.','Komárek (1998)',NULL,0,1),(256,212,'description','Filamentous - thallous; filaments isopolar, contain one or more &nbsp;trichomes placed together and more or less parallely within one sheath, &nbsp;joined and coiled into the spread, macroscopic, gelatinous up to &nbsp;leathery, irregularly clathrate or compact, dirty green mat. Trichomes &nbsp;uniserial not branched (but after &nbsp;disintegration they remain parallely &nbsp;situated in the common sheath = similarity with false branching of <em>Blennothrix </em>or <em>Coleodesmium</em>), &nbsp;isopolar, of the same width along the whole trichome, without narrowed &nbsp;and elongated terminal cells, clearly constricted at cross walls. &nbsp;Sheaths firm, more or less thin, structureless, colourless, limited,up &nbsp;to 30 μm wide; sheaths with more trichomes sometimes divaricate, ramify &nbsp;and later split from one another, but remain in one thallus, more or &nbsp;less parallely and later irregularly arranged in one gelatinous mat. &nbsp;Cells barrel-shaped, longer or shorter than wide, pale blue-green. &nbsp;Heterocytes intercalar, barrel-shaped up to cylindrical. Akinetes arise &nbsp;solitary, always paraheterocytic, elongated, ellipsoidal. Cells divide cross-wise by binary fission; without meristematic zones, &nbsp;all cells capable to divide. Reproduction probably by hormogonia.','Komárek (1992)',NULL,0,0),(257,212,'description','Filamentous - thallous; filaments composed from one to more parallely arranged trichomes enveloped by limited, thin or thick, firm or gelatinous sheaths, single or many together, joined more or less in a mucilaginous mat or forming fasciculate or clustering colonies. Trichomes simple, not branched, not attenuated to the ends, of the same width along the whole length, uniserial, moniliform, clearly constricted at cross walls, probably isopolar and metameric. Sheaths colourless, structureless. Cells subspherical or barrel-shaped, not elongated to the ends. Heterocytes interca1ar, probably only single, several in a trichome. Akinetes not known. Reproduction was not described. Cells divide evidently cross-wise along the whole trichome, reproduction probably by hormogonia.','Komárek (1992) sub <em>Hormothamnion</em>',NULL,0,0),(258,205,'description','Filamentous; filaments solitary or in groups, heteropolar, attached with one end to the substrate (usually by a mucilaginous pad) and with free second end, erected or irregularly waved and creeping on the substrate, with simple, firm, thin sheath enveloping the trichome and open at the apex, colourless or coloured (yellow-brown, violet). Trichomes up to 15 um wide at the base, uniserial, simple, +/- straight or waved, from the widened base continually attenuated to the ends up to a thin cellular hair (subg. Homoeothrix), or thin and cylindrical along the greatest part of a trichome and at the end hair-like elongated (Subg. Tapinothrix; probably different genera); at crosswalls usually constricted, rarely unconstricted; rarely false branching with one lateral branch, after division at necridic cells or between two vegetative cells (7; different genera 7). Cells shorter than wide or more or less isodiametric, rarely longer than wide before cell division, cylindrical or barrel-shaped, usually pale blue-green, olive-green or greyish, rarely (in large species) blue-green, without aerotopes; hair cells usually vacuolized. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(259,207,'description','Filamentous; solitary, free-living trichomes or small groups of trichomes. Trichomes with a limited growth, more or less short (up to 30 cells per trichome), rarely long with many cells (in cultures), up to 140 um long, 4-12 um wide, simple, isopolar, uniserial, unbranched, sheathless, straight, sightly irregularly waved or semicircular curved, not attenuated at the ends, constricted or unconstricted at the cross walls. Trichomes immotile, easily disintegrating into short segments (immotile<br> hormocytes). Cells always shorter than wide, rarely up to almost isodiametric, shortly cylindrical or barrel-shaped, end cells widely rounded, without aerotopes, thylakoids irregularly coiled, +/- perpendicularly situated to the longitudinal cell walls. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(260,208,'description','Filamentous - thallous; filaments composed from one to more parallely arranged trichomes enveloped by limited, thin or thick, firm or gelatinous sheaths, single or many together, joined more or less in a mucilaginous mat or forming fasciculate or clustering colonies. Trichomes simple, not branched, not attenuated to the ends, of the same width along the whole length, uniserial, moniliform, clearly constricted at cross walls, probably isopolar and metameric. Sheaths colourless, structureless. Cells subspherical or barrel-shaped, not elongated to the ends. Heterocytes interca1ar, probably only single, several in a trichome. Akinetes not known.','komárek (1992)',NULL,0,0),(261,211,'description','Filamentous; filaments rarely solitary, Usually joined in flattened mats or small compact strata, composed from gelatinous, longitudinally stratified lamellated, usually colourless, rarely yellow-brown sheaths, which are sometimes diffluent at the margin, enclosing one or several, more or less parallely situated trichomes; old sheaths sometimes densely crosswise lamellated. Filaments sometimes branched (only sheaths). Trichomes cylindrical, usually unconstricted or slightly constricted at the crosswalls, sometimes_slightly narrowed to the ends. Cells more or less isodiametrical or slightly shorter or longer than wide; end cells cylindrical or conical, outside rounded, sometimes with thickened outer cell wall or with narrow calyptra. At cross walls slight granulation. Trichomes are usually motile (gliding) within sheaths.','komárek (1992)',NULL,0,0),(262,209,'description','Unicellular - colonial; colonies microscopic, composed from thick mucilaginous, colourless, usually more or less crosswise lamellated (additional growth zones) stalks, at the bases confluent and sometimes pseudodichotomously branched, usually joined to the substrate, at the upper end or in apical parts with freely disposed cells. Cells solitary, in groups or loosely arranged in short rows, widely oval, oval or cylindrical with rounded ends, blue-green, with homogeneous or slightly granular content.','komárek (1992)',NULL,0,0),(263,210,'description','Cells grouped initially into unilayered, pseudoparenchymatous, nemato- or blas- toparenchymatous colonies, more or less circular in outline, covering the substrate (stones, plants), from which radially oriented rows of tightly packed cells grow on the margin; old colonies remain monolayered, or erect pseudofilaments (?) grow in the center, which are more or less parallel to one another, or form aggregates of clustered cells; pseudofilaments enveloped by thin, colourless sheaths; sheaths laterally confluent. The cells in old colonies form flattened layers up to hemispherical formations, or thin or thick, on the surface granular, black- green, black-brown or violet macroscopic mats. In old parts of the thallus are the cells or their groups (usually with 4-8 cells) more distant from one another, enveloped by their individual mucilaginous sheaths, sometimes even forming sarcinoid packets. Cells are spherical, oval, irregular or elongate at the ends of pseudofilaments, pale blue-green or olive-green, with more or less homogeneous content.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(264,210,'description','Unicellular - colonial; cells gathered firstly into unilayered , pseudoparenchymatous, nemato- or blastoparenchymatous, more or less circular colony covering the substrate (stones, plants), from which grow on the margin radially oriented, tightly gathered rows of cells; in old colonies develop erected pseuaofilaments. Pseudofilaments are situated parallely unbranched or later pseudodichotomously or pseudotetrachotomously divaricated, enveloped by thin, colourless sheaths; sheaths confluent together by their sides. Old colonies hemispherical, or forming thick, on the surface granular, black-green, black-brown or violet macroscopic mats. In old parts of thallus are the cells or their groups (usually with 4 or 8 cells) more separated, enveloped their own mucilaginous sheaths, sometimes forming even sarcinoid packets.˝ Cells spherical, oval, irregular or elongated at the ends of pseudofilaments, pale blue-green or olive green, with more or less homogeneous content.','komárek (1992)',NULL,0,0),(265,215,'description','Filamentous – thallous; thallus flat, covering the substrate in form of the irregular crustaceous monolayer or of dark green or blackish spots, with heteropolar filaments, arranged parallely and densely into one-layered stratum, oriented perpendicularly to the substrate. Trichomes straight or slightly waved, uniseriate, with basal heterocytes, more or less cylindrical from the basis along the main part of the whole trichome length, in the apical part successive narrowed and elongated in short or long, cellular hair with intense constrictions at cross-walls. Sheaths fine, gelatinous, indistinctly stratified, colourless or yellow-brown, soon gelatinizing, diffluent and confluent together (trichomes are at last embedded by gelatinous mass, striated parallely with trichomes - rests of gelatinized sheaths). False branching in upper part of trichomes separated trichomes remain parallely joined to the original one, but not in direct connection. Cells barrel-shaped, in the hair cylindrical, with blue-green, slightly granular content. Heterocytes basal, hemispherical or spherical, before false branching also intercalar, which usually soon obtain the spherical form. Akinetes missing.','komárek (1992)',NULL,0,0),(266,213,'description','Thallus highly differentiated, composed of irregular, more or less ramified (rarely simple) pseudofilaments, creeping on calcareous substrates (usually limestone or shells of molluscs, rarely on other stones or on plants), but mainly euendolithic (or endophytic) growing into the substrate (boring types). Pseudofilaments with one or more rows of cells, sometimes in older parts are formed irregular groups of cells, often nematoparenchymatously arranged; pseudofilaments usually laterally (rarely pseudodichotomously) divaricate. Thus, thallus is differentiated into (1) initial, epilithic or superficially endolithic part, from which grow (ii) pseudofilaments into the substrate (sometimes with branching); apical parts of endolithic pseudofilaments (i.e., deepest parts in the substrate) are usually morphologically different from initial pseudofilaments. Mucilaginous sheaths are firm, thick, usually layered, rarely gelatinized and commonly visible also between cells. Cells more or less spherical, subspherical, oval or rounded polygonal, of diverse size, sometimes distinctly elongate, cylindrical, ovoid, at the ends of pseudofilaments oval or club-shaped (rarely hemispherical). Thylakoids irregularly arranged (<i>H. balani</i>, <i>H. caespitosa</i>).','komárek & anagnostidis (1998)',NULL,0,0),(267,213,'description','Pseudofilamentous; thallus composed from filament-like, irregular rows of cells creeping on substrate (usually carbonate rich) or/and boring it. Initial (surface) stages are gathered cell groups enveloped by own, distinct, colourless, firm sheaths (chroococcalean stages). Pseudofilaments grow into the stony substrate from the ˝basal nematoparenchymatous colony, uniseriate or (rarely) polyseriate, laterally pseudobranched (divaricated) with different frequency, enveloped by thin or thickened, firm or mucilaginous, sometimes layered sheaths, straight or slightly curved, at the ends with distinctly elongated terminal and subterminal cells.','komárek (1992)',NULL,0,0),(268,214,'description','Filamentous - thallous; thallus composed from creeping and/or erect filaments with common, irregular and repeated true, pseudodichotomous branchings, more or less polarized. Trichomes and branches of the same morphology, moniliform, torulous, uniserial and later multiserial (up to with five cells), in old basal parts sometimes forming chroococcoid clusters of cells; branchings of V- and T- type (latter in young, creeping trichomes). Sheaths thin, homogeneous, colourless up to thick, clearly stratified<br> and coloured (yellow-brown), enveloping the whole branched trichome. Cells subspherical, polygonal-rounded or barrel-shaped (in uniseriate trichomes), blue-green or violet, finely granulated. Heterocytes solitary, intercalar, usually flattened, shorter than wide. Akinetes not known.','komárek (1992)',NULL,0,0),(269,217,'description','Filamentous - thallous; thallus attached in tufts, composed from basal, pseudo- dichotomously branched, coiled and more or less prostrate filaments and upper unbranched, free, erect filaments arising from lower trichomes after true branching. Trichomes uniserial, composed from cylindrical cells in young and apical trichome parts and from barrel-shaped cells in older trichomes; trichomes are true branched (typical reverse V-type, less frequently lateral T-type); young trichomes and branches  are continually:attenuated to the ends, forming cellular, cylindrical, narrow and long hairs with elongated cells. Sheaths present, wide, co1ourless, enclosing one or more trichomes, in lower parts lamellated, divergent. Cells shorter than wide in lower trichomes and up to ten times longer than wide in hairs. Heterocytes absent, akinetes arise in short rows at old parts of trichomes, subspherical, a little larger than vegetative cells, with thickened, dark cell wall.','komárek (1992)',NULL,0,0),(270,216,'description','Filamentous; filaments solitary, in small,microscopic fascicles or in formless, microscopic, gelatinous colonies, attached to the substrate, in metaphyton or free floating, with fine, diffluent, structureless, colourless, sometimes hardly visible gelatinous envelopes. Trichomes uniserial, simple curved or coiled, isopolar, usually slightly narrowed to both ends, clearly constricted at cross walls. Cells barrel-shaped, isodiametrical or longer or shorter than wide, sometimes with solitary granules within cells. Heterocytes missing. Akinetes arise in rows, more or less in the middle of tricho- mes (apoheterocytic orimin), a little larger than vegetative cells, with thick cell walls.','komárek (1992)',NULL,0,0),(271,219,'description','Solitary pseudofilaments, unbranched or rarely laterally or pseudodichotomously divaricate (and occasionally anastomozing), straight or slightly wavy, consisting of one row of transversally located narrow-oval cells, situated perpendicularly to the longitudinal axis of the pseudofilaments. Mucilaginous envelopes tube-like, colourless, structureless, slightly diffluent or more or less distinct at the margin, rounded at the ends. Clear spaces are visible between cells, only after division the daughter cells remain together. Cells discoid, in lateral view transversally narrow-oval pale grey-blue or blue-green with fine granular content without gas vesicles, apical cell rounded. Pseudofilaments sometimes contain numerous necridic cells.','komárek & anagnostidis (1998)',NULL,0,0),(272,219,'description','Unicellular - pseudofilamentous; pseudofilaments free living or in small groups, solitary, cylindrical, up more than 1 mm long, uniseriate, very rarely pseudodichotomously divaricated and again joined, composed from the simple row of ˝transversally elongated˝, more or less discoid cells, which are oriented by their ˝longer˝ axis cross-wise to the axis of pseudofilaments and of the enveloping sheath. Sheaths gelatinous, colourless, not layered, fine, thin up to slightly widened from cells and sometimes diffluent at the margin. Cells are slightly or clearly distant one from another, only after division the daughter cells remain joined short time together; divarication starts after the shift of one daughter cell from the original direction of pseudofilament and by the following division of both daughter cells. Cell content pale blue-green or olive- green, homogeneous or finely granular.','komárek (1992)',NULL,0,0),(273,221,'description','Filamentous; filaments (trichomes) solitary or agglomerated in clusters or in fine, mucilaginous colonies (mats), straight or slightly waved or arcuated, moniliform, simple, short or (rarely) long (up to 650 um), without firm sheaths, sometimes with very fine, diffluent, colourless, narrow mucilaginous envelope (staining !); trichomes deeply and widely constricted, not attenuated towards the ends, with indistinct motility (trembling). Cells more or less spehrical or barrel-shaped, up to 10 μm wide, without gas vesicles, sometimes with irregularly dispersed prominent granules; end cells rounded (subg. Abys- sophoron) or with conical outer<br> cell walls (subg. <i>Komvophoron</i>).','komárek (1992)',NULL,0,0),(274,222,'description','Thallus endolithic, irregular, isopolar, composed from more or less parallely situated filaments, without false or true branchings, but with common lateral loops, rounded at the ends; filaments in loop-like formations grow tightly aside, parallely. Trichomes uniserial, isopolar, with more or less isodiametric cells, clearly constricted at cross-walls, narrowed to the both hair-like ends up to the sharply pointed terminal cells. Sheaths firm, colourless, slightly widened, not gelatinizing. Heterocytes present, intercalar. Akinetes missing.','Komárek (1992)',NULL,0,0),(275,220,'description','Filamentous; solitary trichomes or (extraordinary) small clusters of several trichomes, free-floating or free-living among other algae. Trichomes rarely straight, usually irregularly coiled up to screw-like coiled, 10-30 μm wide, usually with a limited growth, rarely long and multicelled, simple, uniserial, unbranched, without firm sheaths, but enveloped by a wide, colourless, sometimes diffluent mucilaginous envelope; trichomes at the ends not attenuated or only with few (-5) last cells slightly narrowed, sometimes with calyptra, at the cross walls constricted or unconstricted. Trichomes immotile, easy disintegrating into motile hormocytes (or with indistinct, slow and interrupted trembling without envelopes). Cells always shorter than wide, shortly cylindrical or barrel-shaped, without or with aerotopes (planktic species); thylakoids irregularly coiled with reticular arrangement through the cell. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(276,223,'description','Filamentous; filaments solitary, rarely (in old stages) tangled together, isopolar, waved or irregularly spirally coiled (particularly in the middle parts), sometimes with more or less erected and free ends, creeping on the substrate (usually coiling about other filamentous cyanophytes or algae) and attached to it by the central part, with simple, firm but thin, colourless sheath enveloping the trichome and opened at the apex, unbranched or very rarely falsely branched (usually with one lateral branch), 1.5-12 (?) μm wide. Trichomes cylindrical, with cylindrical cells, sometimes with a little modified morphology of cells in apical parts (trichome ends more constricted at cross walls or slightly widened), unconstricted or constricted at the cross walls in the middle part, not attenuated, immotile. Cells +/- isodiametric, slightly shorter or up to distinctly longer than wide, cylindrical or sometimes barrel-shaped at the ends, without aerotopes, pale greyish, blue-green or yellowish; end cells rounded, without thickened cell wall or calyptra. Heterocytes and akinetes lacking.','komárek (1992)',NULL,0,0),(277,226,'description','Thallous; thallus composed from free, separated, initially creeping filaments and later erected branches; filaments more or less densely parallely situated forming Symploca-like fascicles. Trichomes uniserial, only rarely with cells dividing lengthwise and laterally branched (V- and T- type). Cells barrel-shaped (forming torulous trichomes) in old filaments with thickened, usually brownish sheaths, young trichomes and branches with cylindrical cells, with thin, colour less sheaths. Heterocytes intercalar, rarely lateral. Akinetes missing.','komárek (1992)',NULL,0,0),(278,218,'description','Filamentous; filaments usually solitary or freely clustered (tangled and coiled) into small colonies, rarely forming macroscopically visible mats; trichomes always without sheaths, cylindrical, isopolar, usually wawed or coiled, narrow, thin, 0.5-3 μm wide, uniseriate, usually not narrowed to the ends, slightly constricted or unconstricted at the cross walls, always immotile. Cells cylindrical, elongated, longer than wide (up to several times), without aerotopes, sometimes with solitary granules (rarely at the cross walls); end cells rounded_or narrowed, pointed or conical – rounded, always - without calyptra. Cell content pale blue-green, grey, yellowish or olive-green; in some species ability of chromatic adaptation (changeable phycobiline ratio).<br>Cell division by the crosswise binary fission, perpendicularly to the &nbsp;long axis of a trichome, daughter cells grow +/- up to the original size &nbsp;before the next division. All cells capable to divide. Reproduction by &nbsp;the fragmentation of trichomes without necridic cells into immotile &nbsp;hormocytes (indistinct motility was not proved yet).','Komárek (1992)',NULL,0,0),(279,228,'description','Cells irregularly deposited in wide, homogenous, amorphous, colorless, and diffluent mucilage, distant one from another in microscopic colonies usually of a small number of cells (2-40). Cells spherical, after division subspherical, up to 22 um in diameter, usually with gray-green, bluegreen, or olive-green content. Cell division by binary ission, in 2-3 planes in successive generations. The cells reach the original spherical shape before the next division. Reproduction proceeds by disintegration of colonies or liberation of cells from colonies.','komárková et al. (2010)',NULL,0,0),(280,229,'description','Filamentous; filaments solitary, free floating, straight or slightly curved or irregularly screw-like coiled, many-celled, isopolar, without sheath or with very fine, colourless , facultative sheath (in several species). Trichomes cylindrical, composed from cells which are isodiametric or longer than wide (sometimes several times), unconstricted or slightly constricted at the cross walls, with very thin walls, with missing or very reduced motility, 1-6 um wide, not tapering to the ends, usually with cylindrical (but sometimes with conical) apical cells, without terminal calyptra (but rarely with conical plasmatic protrusions). Cells pale blue-green, yellowish or pinkish, able to produce facultative gas vesicles; aerotopes are localized at the ends of cells, or united into long, large, central aerotope; thylakoids sometimes slightly waved, localized parallely along the cell walls. Phycobiline composition changeable (with unstable phycoerythrin/phycocyanin ratio). Known involution cells. No toxic strains. Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(281,227,'description','Thallous; thallus joined to the substrate, more or less hemispherical, macroscopic (up to 2 mm in diameter), gelatinous, firm, composed from more or less straight, polarized, branched, more or less erected filaments. Filaments situated more or less parallely and near one to another, radially oriented, with true branchings (V- type). Sheaths colour less in young filaments, later yellow to brown, thick, lamellated. Trichomes uniserial, composed from barrel-shaped, mainly isodiametric cells. Heterocytes very rare, intercalar.','komárek (1992)',NULL,0,0),(282,224,'description','Colonies microscopic, in form of mucilaginous spheres, simple or compound, with several spherical subcolonies, sometimes slightly irregular oval, free floating in plankton or metaphyton, consisting of fine, homogeneous, colourless mucilage; beneath the surface is a layer of irregularly, more or less tangentially arranged cells, sometimes overlapped by a thin, but distinctly delimited layer of colonial slime. Cells oval or rod-shaped, up to several times longer than wide, usually slightly distant one from another or in small clusters, pale blue-green, without aerotopes. Without stalks in the colonial center.','komárek & anagnostidis (1998)',NULL,0,0),(283,224,'description','Unicellular - colonial; colonies microscopic, spherical, irregularly spherical up to irregular, mucilaginous, free living (mainly floating) in freshwater reservoirs, with cells situated more or less in the peripheral layer, without any mucilaginous stalks. Cells are oval to rod-like, without aerotopes, placed in the surface layer tangentially and irregularly or in small groups, sometimes more or less parallely. Mucilage is colourless, fine, limited or diffluent, sometimes slightly concentrically lamellated.','komárek (1992)',NULL,0,0),(284,225,'description','Filamentous; filaments long, solitary or coiled into clusters and fine mats (which are sometimes up to macroscopic and several cm in diameter), arcuated, waved or intensely coiled, isopolar, thin, fine, 0.5-3.2 um wide, with simple, thin but firm, usually colourless facultative sheaths opened at the apical end; sheaths joined to the trichomes or slightly distant from them, enveloping only one, very rarely (in short sections) two trichomes; rarely up to very rarely false branching (more common under special cultivation conditions), usually with only one lateral branch. Trichomes fine, cylindrical, usually not attenuated to the ends or slightly attenuated, with rounded or conical apical cells, not constricted or constricted at the cross walls, immotile. Cells +/- isodiametrical or longer than wide (up to several times), cylindrical, with +/- homogeneous content, without aerotopes, rarely with scarce prominent granules, pale blue-green, greyish, olive-green, yellowish or reddish; end cells without thickened cell walls or calyptras. Heterocytes and akinetes are absent.<br>Cells divide by +/- symmetrical (rarely asymmetrical) crosswise binary &nbsp;fission, cells grow into original size before next division. &nbsp;Reproduction by motile (?) hormogonia, liberating from trichomes at &nbsp;their ends, fragmentated without help of typical necridic cells, but &nbsp;sometimes after death of sacrifying cells.','Komárek (1992)',NULL,0,0),(285,232,'description','Thallous; filaments heteropolar, attached by one end to the substrate, erected, near the base laterally branched (true branching of the V- type?), joined into blue-green, up to 1 mm long, more or less rigid fascicles. Filaments (trichomes) sheathless, always uniserial, at the end narrowed in a long cellular hair, at the base 2-4 μm wide, constricted at the cross-walls. Cells cylindrical, longer than wide. Heterocytes and akinetes not observed.','komárek (1992)',NULL,0,0),(286,231,'description','Cells irregularly arranged in macroscopic, flat, originally slimy and later hard, crustose colonies, usually heavily encrusted by lime. Cells are enveloped by their own gelatinous envelopes. Cells are spherical to oval and short cylindrical, slightly distant from one another, rarely in groups, only slightly over 1 μm in diameter, with no obvious gas vesicles, and pale blue-green. Cell division probably is in one plane in successive generations.','Komárek (2003)',NULL,0,0),(287,231,'description','Unicellular - colonial; colonies mucilaginous, micro- up to macroscopic, covering the stony substrate as a gelatinous mat, with numerous ca1careous precipitations up to hard, intensely calcified. Cells arranged in the colony irregularly, sometimes gathered in small, 2-, 4- to more-celled groups, with their own mucilaginous envelopes, which are more or less homogeneous, not layered, colourless, diffluent and confluent by their margins in a homogeneous mass; cells spherical, ovoid up to shortly cylindrical, very small (below 1 μm wide), pale blue-green or greyish up to colourless.','Komárek (1992)',NULL,0,1),(288,231,'description','Colonies distributed over a substrate, crustose, usually heavily incrusted with lime, hard, primarily composed of a mucilaginous layer of homogeneous slime with irregularly arranged cells (never in rows), surrounded by their own gelatinous, diffluent envelopes. Cells more or less spherical, ovoid or short cylindrical, sometimes aggregated into small, 2-, 4- or few-celled, irregular groups.','Komárek & Anagnostidis (1998)',NULL,0,1),(289,230,'description','Colonies endolithic, irregularly reticulate, composed of randomly divaricate and anastomozing,<br> more or less limited and firm mucilaginous, filamentous strands, colourless, homogeneous, inside with uniseriate, irregular rows of cells, oriented parallel to the strands; in places with widened mucilage, the cells are irregularly distributed; without special envelopes around them. Cells spherical, ellipsoidal<br> or oval, near to one another after division.','komárek & anagnostidis (1998)',NULL,0,0),(290,230,'description','Unicellular - colonial; colonies endolithic, filamentous, irregularly net-like, composed from thin, mucilaginous strings, in which the cells are arranged in irregular rows with cells clearly distant one from another; old parts of strings are widened with irregularly disposed cells. Mucilaginous strings homogeneous, without any structures, special envelopes around solitary cells are missing. Cells spherical, ellipsoidal or oval','komárek (1992)',NULL,0,0),(291,230,'description','Lager endolithisch, fadenförmig, wiederholt „verzweigt˝. Zellen meist ellipsoidisch, seltener kugelig, in dicken Lagerteilen regellos, in dünnen parallel zur Längsachse der „Fäden˝ gestellt, in den jüngsten Teilen in einer Reihe. Keine Spezialhüllen: Zellen in homogener, kaum sichtbarer Gallerte.','Geitler (1932)',NULL,0,0),(292,235,'description','Filamentous; filaments more or less parallely and densely joined in fascicles and perpendicularly oriented to the substrate, radially composed in macroscopic, hemispherical colonies or (later) in thick layers, attached to stones and sometimes incrusted, or covered by anorganic particles; filaments always with colourless, firm sheaths, which are joined to trichomes, often branched and anastomozing (only sheaths, not trichomes) and enveloping one, rarely two trichomes, opened at the ends, rarely ,crosswise lamellated. Trichomes isopolar, cylindrical, 5-8 μm wide, with or without slight constrictions at the cross walls, at the end not attenuated, with the end cell widely rounded, with thickened outer cell wall. Cells more or less isodiametric or slightly longer or shorter than wide, without aerotopes, olive-green or blue-green, slightly granular. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(293,233,'description','Thallous; thallus attached to the substrate, grass-like, composed from more or less rigid, erected, regularly and repeatedly pseudodichotomously divaricated free filaments. Trichomes always uniserial, constricted at the cross walls, composed of short, more or less isodiametric and barrel-shaped cells, with rounded-conical apical cells, true-branched (V-type). Sheaths thick, not confluent, distinctly limited, intensely lamellated, funoel-like with diverging layers, but not widened at the ends, incrusted by lime; the ends of layers causes the transverse lamellation on the sheath surface. Heterocytes present, solitary, intercalar, rarely terminal at the ends of branches; sometimes they occur near the bases of branches. Akinetes develop occasionally in rows, oval or ellipsoidal, slightly larger than are the vegetative cells, but with thin cell wall (?).','komárek (1992)',NULL,0,0),(294,237,'description','Cells occur in flat, microscopic formations attached to substrata (as epiphytes on other algae) in one layer and arranged more or less in perpendicular rows. Cells are spherical, pale blue-green or reddish in color, have homogeneous content or distinguishable centro- and chromatoplasm, and are 0.8-4 μm in diameter. Cells usually are enveloped by thin, very fine, colorless, and diffuse mucilage. Division is by binary fission, in two planes perpendicular to one another and to the substrate; from this process, flat formations arise on the substrate, but sometimes have slightly shifted cells.','komárek (2003)',NULL,0,0),(295,237,'description','Small, more or less spherical cells, solitary or in groups (in one layer), attached on the substrate (usually epiphytic on other algae and filamentous cyanoprokaryotes), forming one-layered colony; cells are usually arranged in perpendicular rows on a substrate (sometimes indistinct; result of cell division in two perpendicular planes). Cells more or less spherical, usually without distinct mucilaginous envelopes (but with basal gelatinous discs ?).','komárek & anagnostidis (1998)',NULL,0,0),(296,237,'description','Unicellular; cells solitary or in flat groups, arranged in one plane (layer), sometimes more or less in irregular rows, joined to the substrate (by mucilaginous pads ?), but not evidently heteropolar, usually more or less spherical or slightly oval, with homogeneous or slightly granular content. Without mucilage. Attached usually to other filamentous algae.','komárek(1992)',NULL,0,0),(297,236,'description','Cyanobacterial, heterocytous, filamentous genus. Filaments are free-living, solitary, in small irregular clusters or in fine macroscopic mats.<br>Trichomes have symmetric to subsymmetric structure with two subapical heterocytes and sometimes with one ± central heterocyte; they are nearly straight or irregularly coiled with fine, colourless, diffluent and indistinct slime, uniserial, unbranched, ± cylindrical, constricted at crosswalls, sometimes narrowed to the ends and in distinct central parts. Cells cylindrical or slightly barrel-shaped, ± isodiametric or rather longer than wide, with blue-green, homogeneous content with scarce granules and facultatively with solitary aerotopes; terminal cells are rounded, conical or narrowed and bluntly pointed. Heterocytes always solitary, intercalar, cylindrical, usually wider than vegetative cells, usually two in subapical position in a trichome, or with the third heterocyte ± in the middle of a trichome. Akinetes widely oval, developing from several neighbouring cells, large, solitary, rarely in pairs, always attached to outer heterocytes; in one trichome develop usually only two akinetes, outside from heterocytes, rarely also at the “inner” side of a heteocyte.','Komárek (2008)','[251]',0,0),(298,234,'description','Filamentous; filaments thick, rarely solitary, usually connected into thick, layered, sometimes leathery strata (mats), rarely tangled into free clusters of coiled filaments, usually macroscopic, up to several cm or dm in diameter, with firm sheaths, which are sometimes layered or stratified and brownish coloured, opened at the ends; very rarely without sheaths (usually only reproduction hormogonia); unbranched or slightly falsely branched with short and sporadical branches. Trichomes isopolar, straight or slightly waved, thick (5.5-60 um), uniserial, composed of shortly cylindrical or barrel-shaped discoid tells, unconstricted or constricted at the cross walls, not attenuated or attenuated to the ends, not motile or slightly motile (but with motile hormogonia !). Cells very short, always shorter (usually several times) than long, without or (rarely) with facultative aerotopes, usually finely granulated, sometimes more at the cross walls; cell content blue-green, olive green, yellowish, brownish or pinkish, with coiled tylakoids, situated more or less over the whole cell content; end cell with thickened outer cell wall or with prominent calyptra. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(299,241,'description','Thallous; thallus composed from free, densely irregularly coiled, creeping filaments. Sheaths thin, firm, colourless, homogeneous. Trichomes always uniserial, with cylindrical cells, not or slightly constricted at cross walls, commonly irregularly laterally true-branched; branching of T- type; branches more or less short, 1-2- few-celled, terminated by apical, unipored heterocytes or long, continually tapering to the hair-like ends. Cells more or less isodiametric or longer than wide (especially in ends of branches), blue-green or pinkish. Heterocytes terminal at branches or lateral (laterally attached to trichomal cells), rarely interkalar, usually solitary, rarely in pairs. Akinetes missing.','komárek (1992)',NULL,0,0),(300,239,'description','Thallous; thallus in a form of soft, spongy mats, sometimes with small lime crystalls, smooth or gelatinous at the surface, up to compact, ocasionally layered, dirty blue-green or olive green, composed from more or less densely tangled filaments. Trichomes uniserial, irregularly coiled, with thin, distinct, colourless sheaths, which diffluent in old stages; true branching of T- or reverse Y- type, often unilateral, in some stages the branching is rare or almost absent; branches usually continually tapering to the ends. False branching also facultatively present, but not common. Heterocytes intercalar, solitary or (rarely) in pairs. Akinetes very rare, solitary in old parts of trichomes.','komárek (1992)',NULL,0,0),(301,240,'description','Thallous; thallus in a form of thin mats, composed from free, irregularly coiled filaments. Filaments with thick, firm, homogeneous or layered, diverging, colourless, sometimes transversally constricted sheaths. Trichomes uniserial with isodiametrical and more or less long, cylindrical cells with blue-green content, constricted at cross-walls. True branching common, lateral, of T- and v-type; branches long, continually tapering to the ends (but not forming terminal hairs; the hair-like ends are thin rests of empty sheaths ?), or short, cylindrical. Heterocytes and akinetes not known.','komárek (1992)',NULL,0,0),(302,238,'description','Thallous; filaments sheathed and true branched, flexuous, creeping on the substrate or tangled in clusters. Sheaths thin, colourless, not lamellated. Trichomes uniserial, constricted at cross-walls, with T- or reverse V-like branching; branches usually slightly thinner than main trichomes, sometimes slightly attenuated towards_the ends; terminal cells elongated, rounded. Cells more or less barrel-shaped (in main trichomes) up to cylindrical in branches, isodiametrical or distinctly longer than wide. Heterocytes intercalar (bipored), more or less spherical, wider than vegetative cells or lateral (unipo- red), attached to the vegetative cells or at the ends of short branches (with 1 or few cells). Akinetes not observed.','komárek (1992)',NULL,0,0),(303,242,'description','Thallous; thallus in a form of thin mat, covering the substrate, grey-green, composed from densely, more or less paralely situated, slightly irregularly waved, creeping filaments; sheaths thin, homogeneous, sometimes laterally confluent. Trichomes always uniserial, cylindrical, commonly irregularly branched (V-type), with barrel-shaped and cylindrical, more or less isodiametric cells (moniliform-torulous and cylindrical segments irregularly alternate along trichomes). Heterocytes intercalar.','komárek (1992)',NULL,0,0),(304,246,'description','Colonies microscopic to macroscopically visible, flat, tabular, free-living, mucilaginous,<br> composed of one layer of densely packed cells, sometimes composed of subcolonies; cells sometimes arranged in perpendicular rows (usually in young colonies), later quite irregularly (in several species rows of cells rarely are formed); mucilage colourless, cells without individual mucilaginous envelopes. Cells elongate, ellipsoidal, oval or rod-shaped, with rounded ends, oriented with their longer axis perpendicular to the plane of colony (during the life cycle stages with rounded cells occur). Thylakoids (in <i> M. geminata</i>) are wavy and disposed through the whole cell content (Chang in litt.).','komárek & anagnostidis (1998)',NULL,0,0),(305,246,'description','Unicellular - colonial; colonies many-celled, microscopic, rarely macroscopically remarkable (with many cells), table-like, flat or slightly waved, uniserial, mucilaginous, usually with irregular outline, with cells gathered in one layer in the plane of colony; in young colonies are the cells more or less in rows perpendicular one to another, in old colonies irregularly and usually very densely gathered, in several cases up to polygonal in outline (subg. Beckia). Mucilaginous envelope fine, colourless, diffluent; cells without their own mucilaginous envelopes. Cells rarely spherical when young, later (at least in a part of the life cycle)<br> elongated, situated perpendicularly to the plane of colony, widely oval, oval up to rod-like, with rounded ends, sometimes several hundreds in a colony; cells usually without visible chromatoplasma (irregular arrangement of thylakoids within the cells).','komárek (1992)',NULL,0,1),(306,246,'description','Zellen zu tafelförmigen Kolonien von mehr oder weniger unregelmäßigem Umriß vereinigt, ellipsoidisch bis zylindrisch (die Längsachse senkrecht auf der Fläche der Kolonie stehend), mit abgerundeten Enden, ohne Spezialhüllen, in<br> gemeinsamer Gallerte liegend. Teilungen nach zwei Raumrichtungen, parallel zur Längsachse.','geitler (1932, sub holopedia)',NULL,0,0),(307,247,'description','Colonies micro- or macroscopic, free floating, spherical, oval, lobate to irregular, or elongate, in several species irregularly clathrate, sometimes composed of subcolonies or clustered together, with irregularly, sparsely or (usually) densely arranged cells in common<br> mucilage. Mucilage fine, colourless, usually homogeneous or only indistinctly lamellate, diffluent or distinct and delimited, in several species with refractive outline (surface); around individual cells gelatinous envelopes never present. Cells spherical or hemispherical after division, with gas vesicles (joined into distinct aerotopes). Hexagonal substructure (p6) of S-layers was found in cell walls of several Microcystis strains.','komárek & anagnostidis (1998)',NULL,0,0),(308,247,'description','Unicellular - colonial; colonies gelatinous, free floating or attached to the substrate, microscopic, spherical, discoid or irregular, later usually macroscopic, amorph, irregular, sometimes net-like, with numerous cells without own mucilaginous envelopes, irregularly distributed within the common slime, sometimes densely agglomerated; colonial mucilage colourless, usually homogeneous, fine, diffluent (staining !), rarely with the limited, sometimes refractive margin. Cells spherical or (after division) hemispherical, with homogeneous, blue-green, greyish or yellowish content, in several planktic species with several up to numerous aerotopes; sometimes with visible chromatoplasma. Several strains are toxic, and producing b-cyclocitral.','komárek (1992)',NULL,0,0),(309,247,'description','Zellen kugelig oder länglich, zu vielen in kugeligen, ellipsoidischen, unregelmäßigen oder netzförmig durchbrochenen Kolonien, welche manchmal aus Teilkolonien zusammengesetzt sind, vereinigt. Die Zellen liegen in einer gemeinsamen, homogenen, weichen, typischerweise ungefärbten Gallerthülle, welche manchmal zerfließt; Spezialhüllen zerfließend. Zellen meist sehr dicht gelagert, durch gegenseitige<br> Abplattung oft eckig. Zellteilungen nach allen Raumrichtungen. Teilung bei länglichen Zellen quer zur Längsachse. Nannocyten bisher nur bei Microcystis flos-aquae bekannt. Kolonien meist freischwimmend; Zellen bei vielen Arten mit Gasvakuolen.','Geitler (1932)',NULL,0,0),(310,245,'description','Filamentous; filaments solitary or joined in fine, thin strata or mats. Filaments composed from a gelatinous, fine, usually colourless and diffluent, homogeneous sheath, in which are densely packed trichomes, parallely arranged and sometimes irregularly screw-like coiled together; number of trichomes changes usually from 2-3 up to more than hundred within one filaments; filaments usually simple, rarely simply branched (only sheaths). Trichomes cylindrical, with straight, usually narrowed<br> ends. Cells usually isodiametrical, rarely shorter or longer (up to three times) than wide; end cells usually conical, rarely with calyptra. (Species with very narrow trichomes and cells always clearly longer than wide and small number of trichomes within sheaths belong probably in a special genus of Schizothrichaceae).','komárek (1992)',NULL,0,0),(311,243,'description','Colonies microscopic, rarely (in large species) macroscopic, free-living, tabular, with one layer of densely or loosely arranged cells in the plane of the colony square or rectangular, later sometimes with irregular outline, flat or wavy; large colonies sometimes contorted or composed of several subcolonies. Colonies consist of few to very many (in several species over 4000) cells; cells arranged in perpendicular rows, distant or close together. Colonial mucilaginous envelopes colourless, structureless, hyaline, fine, usually with indistinct narrow or wide  margin; cells sometimes with individual gelatinous envelopes (in several species facultatively so). Cells spherical or widely elliptical (when they are elongate or oval, the longer axis lies in the plane of the colony), after division hemispherical, with homogeneous, pale or bright blue-green or reddish (violet, pink) content; in a few species in central parts of cells appear refractive bodies or aerotopes. The parietal arrangement of thylakoids was found in all up to now studied members of Merismopedia.','komárek & anagnostidis (1998)',NULL,0,0),(312,243,'description','Unicellular - colonial; colonies free floating, microscopic, rarely (in several “large” species) macroscopically visible, usually table-like, flat or slightly waved, with cells situated in one plane, in rows more or less perpendicular one to another (sometimes two or four cells more or less in duplets or quadriplets), squared or rectangular when young, in later stages sometimes irregular or composed from smaller, clustered, table-like colonies; colonies with 4-16, but in several species up to several hundreds of cells (up to 4000); mucilaginous envelope of colonies colour less, usually homogeneous, fine, diffluent at the margin, rarely limited,<br> in few species with ferric precipitations; around cells sometimes own, colourless mucilaginous envelopes. Cells spherical or widely oval (before division), after division hemispherical, with homogeneous content, sometimes finely granular or with visible chromatoplasma, in several planktic species one or more: aerotopes in a cell.','komárek (1992)',NULL,0,0),(313,243,'description','Kolonien tafelförmig, durch regelmäßig abwechselnde Teilungen nach zwei aufeinander<br> senkrecht stehenden Raumrichtungen gebildet, meist, namentlich in der Jugend, eben und quadratisch oder rechteckig, oft im Alter gefaltet oder mehr oder weniger kugelig zusammengerollt und mit einspringenden rechten Winkeln, immer aus einer einzigen Zellage bestehend, in der Regel freischwimmend. Zellen kugelig oder ellipsoidisch bis zylindrisch (im letzteren Fall steht die lange Achse senkrecht zur Ebene der Kolonie), oft in Vierergruppen, mit oder ohne Spezialhüllen, in gemeinsamer Gallerte.','geitler (1932)',NULL,0,0),(314,244,'description','Filaments solitary or in small groups, attached to or creeping on the substrate, heteropolar, with basal heterocytes and free apical ends,more or less cylindrical along the whole length. Sheaths distinct, firm, thin or thick, sometimes slightly lamellated, usually colourless, open at the apex. Whole trichomes cylindrical or slightly attenuated towards the ends (different subgenera ?), constricted or not constricted at the cross-walls, in the apical part sometimes with meristematic zones (shorter cells and deeper constrictions). Cells isodiametric, shorter or longer than wide, cylindrical or rarely barrel-shaped; apical cells always rounded. Heterocytes basal, hemispherical, spherical or slightly elongated and rounded; not frequently also intercalar, cylindrical; rarely false branching at heterocytes. Facultatively develop<br> akinetes, solitary or in rows, near the basis.','komárek (1992)',NULL,0,0),(315,253,'description','Colonies micro- to macroscopic, gelatinous, composed of more or less spherical subcolonies, forming a granular, slimy mass. Subcolonies (1) 2-4-many-celled, enveloped by mucilaginous, wide, stratified or unstratified, sometimes yellow- brownish coloured envelopes, distinctly delimited at the surface. Cells aggregated in the centre of subcolony, oval and slightly arcuate to kidney-shaped, or irregular-rounded after intense division, in an indistinct wreath-shaped<br> arrangement; around cells sometimes indistinctly striated gelatinous envelopes.','komárek & anagnostidis (1998)',NULL,0,0),(316,253,'description','Unicellular - colonial; colonies microscopic, spherical, with one up to many (64) cells irregularly or slightly tangentially agglomerated in the centre of a colony; the cells are enveloped by more or less narraw, own, fine, hyaline or slightly lamellated sheaths, and their groups are situated in a wide, colour- less or yellowish gelatinous envelope, which is slightly concentrically lamellated on the periphery and firmly limited. Cells oval and usually slightly arcuated up to kidney-shaped, with rounded ends, later irregular, rounded-pollygonal. Cell content yellowish or blue-green, homogeneous, with scattered small granules.','komárek (1992)',NULL,0,1),(317,248,'description','Cyanobacterial genus similar to the genus <em>Nostoc</em>. Colonies microscopic in nature, subsphaerical, ellipsoid to irregular, surrounded by a firm and mucilaginous covering. Series of subcolonies create macroscopic, upright or horizontal pseudofilaments in liquid culture. Cells subsphaerical, joined into uniseriate trichomes or strongly flexuous pleuroseriate colonies, strongly constricted at the crosswalls, or agglomerated into dense aggregations. Heterocytes mainly terminal, or lateral in agglomerations, with intercalary heterocytes very rare. Young colonies only with terminal heterocytes. Reproduction with colonial disintegration, by free solitary cells (hormocytes) or multicelled hormogonia. Hormogonia germinating without heterocytes, often with intercalary paired widened cells which often cause acute bending of the hormogonia.','Řeháková et al. (2007)',NULL,0,1),(318,250,'description','Pseudofilamentous; thallus composed from multiseriate, repeatedly irregularly, laterally divaricated (˝branched˝), creeping pseudofilaments, only at the ends uniseriate and with characteristical apical growth, enveloped by fine, thin, mucilaginous, colourless, not layered sheaths, which do not confluent together. Cells more or less separated one from another, within pseudofilaments in irregular nematoparenchymatous rows, or (in basal parts) in pseudoparenchymatous clusters; cells are irregular, apical cells usually a little elongated and rounded.','komárek (1992)',NULL,0,0),(319,250,'description','Thallus in marinen Algen lebend. Fäden mit Ausnahme der Spitze mehrreihig, unregelmäßig seitlich verzweigt, mit deutlichem Spitzenwachstum, frei, nicht seitlich miteinander verwachsen. Membranen mehr oder weniger verschleimend, Zellen daher mehr oder weniger isoliert. Fadenverlauf in alten Lagerteilen oft verwischt. Endoeporen unbekannt.','geitler (1932)',NULL,0,0),(320,252,'description','Thallous; thallus covering the substrate, composed from basal pseudo- or nematoparenchymatous part, in which the cells divide irregularly, and from which grow, the more or less erected, short, densely parallely agglomerated, but well recognizable filaments with confluent, colourless sheaths. Trichomes later multiserial, laterally and pseudodichotomously, repeatedly branched (more or less V-type), slightly narrowed to the ends (hormogonal trichome structure well visible particularly in preserved samples). Cells irregular - rounded, end cell usually conical - rounded; around cells sometimes own, more or less thick, firm or slightly gelatinizing envelopes. Heterocytes and akinetes missing.','komárek (1992)',NULL,0,0),(321,256,'description','Thallous; thallus attached to the substrate, gelatinous, irregularly subspherical, spherical or lobate, with more or less smooth, mucilaginous surface, solid or hollow in the centre, up to 3.5 cm in diameter, bluish, olive-green or yellow-green. Common mucilage usually homogeneous, colourless or yellowish-brown. Filaments oriented indside of colony more or less radially, commonly branched, slightly coiled, with fine, gelatinous, diffluent (mainly in marginal parts), colourless or yellow-brown sheaths. Trichomes always uniserial, composed from isodiametrical, barrel-shaped or elongated (up to twice longer than wide), ellipsoidal, blue green cells. Branching true, lateral (T- or v-type); branches long, many-celled, cylindrical, terminated by slightly narrowed or widened, rounded apical cells; or very short, cylindrical (l-several-celled) branches, terminated by heterocytes. Heterocytes intercalar (bipored), lateral (unipored) o terminal (unipored). Akinetes not known.','Komárek (1992)',NULL,0,0),(322,249,'description','Solitary cells without mucilage or with very fine, narrow individual gelatinous layer, straight or slightly arcuate, several times longer than wide, fusiform, gradually tapering to the ends and pointed or pointed-rounded. Cell content homogeneous, blue-green, olive-green or yellowish, in one planktic species with aerotopes.','komárek & anagnostidis (1998)',NULL,0,0),(323,249,'description','Solitary cells without mucilage or with very narrow fine, diffluent and colourless slime envelope; never in colonies. Cells elongated, spindle-like, continually attenuated to the ends, at the ends bluntly pointed or rounded, more or less straight or slightly arcuated, facultatively with aerotopes and with solitary granules; after division are the cells asymmetrical, with one end more nerrowed, and the second one rounded; the ratio length: width in fullgrown cells always > 10:1, in young cells > 5:1. Ability to form filamentous involutionary cells.','komárek (1992)',NULL,0,1),(324,249,'description','Zellen zylindrisch und an den Enden zugespitzt, oder spindelförmig, oder ellipsoidisch und zugespitzt, gerade oder mehr oder weniger spiralig, S-förmig oder unregelmäßig gekrümmt, selten einzellen, meist zu wenigen in zarter, schwer sichtbarer Gallerte zu Kolonien vereinigt. Teilung quer.','geitler (1932; sub dactylococcopsis, incl. rhabdogloea)',NULL,0,0),(325,251,'description','Cells in small groups (subcolonies) with up to 32 cells, later in packet-like, cubic-rounded or irregular, sometimes slightly flattened or blastoparenchymatous colonies, forming granular mats on the substrate; cells densely packed. Colonies freeliving among other algae or freely on the substrate. Mucilaginous envelopes (sheaths) thin or very slightly widened, distinct, firm, colourless or yellow-brown. Cells rounded polygonal or rounded-irregular, in young colonies in more or less short perpendicular rows, later irregularly disposed.','komárek & anagnostidis (1998)',NULL,0,0),(326,251,'description','Unicellular - colonial; colonies more or less spherical, microscopic, sarcinoid, not polarized, later multicellular, packet-like or sarcinoid, grouped usually densely in irregular agglomerations, enveloped by narrow, tight, fine or firm, colourless, sometimes slightly lamellated envelopes. Cells irregular spherical, later irregular,more or less polygonal with rounded corners; cell content blue-green, olive-green, yellowish or reddish, with solitary granules.','komárek (1992)',NULL,0,0),(327,251,'description','Kolonien abgerundet würfelig, aus dicht gedrängten, far: kubischen oder verschieden abgeplatteten Zellen bestehend, ein Blastoparenchym bildend. Teilungen nach drei Raumrichtunger. die anfangs regelmäßig senkrecht aufeinander stehen; im Alter auch schiefe Teilungen. Membranen dünn, aber deutlich, oder mitteldick. Endosporenbildung.','geitler (1932)',NULL,0,0),(328,254,'description','Filamentous; filaments solitary or in groups or clusters, rarely in mats, isopolar, unbranched (without false or true branching), more or less straight, curved, coiled or irregularly spirally coiled with fine, diffluent sheaths of a special two-layered structure (type species), opened at both ends. Trichomes uniserial, cylindrical, rarely shortly and slightly attenuated at the ends of developed trichomes, constricted at cross walls, metameric, with more heterocytes in more or less regular distances from one another. Cells shortly barrel-shaped, their length never exceeds the width, with (planktic species) or without (benthic species) gas vesicles joined in the aerotopes (two mentioned groups of species differ cytologically and ecologically - subgenera ?); gas vesicles occur facultatively only in planktic species. Cell content yellowish, pale olive-green or blue-green, thylakoids irregularly coiled, spread allover the cell volume, sometimes more gathered in the peripheral layer of cells. Heterocytes of the same shape of cells, sometimes slightly differ in their size (slightly smaller or larger than vegetative cells). Akinetes shortly barrel-shaped (shorter than wide), or spherical, developing apoheterocytic, but often with irregularities.','komárek (1992)',NULL,0,0),(329,255,'description','Thallous; thallus micro- or macroscopic, gelatinous, amorph or spherical, later irregularly spherical, lobate, smooth or warty on the surface, filamentous or forming flat gelatinous or ˝paper-like˝ (when dry) colonies, usually with distinct periderm on the colonial surface. Filaments within colony irregularly coiled and loosely or densely agglomerated, sometimes more gathered in peripheral layer; sheaths around trichomes present, but visible usually only in the periphery of colony or in young colonies, wide, fine mucilaginous, confluent with colonial mucilage, sometimes yellowish-brown. Trichomes isopolar, of the same width along the whole length, apical cells morphologically not different from other cells; cells cylindrical, barrel-shaped up to almost spherical (forming moniliform trichomes; variability of cell-size and -shape sometimes distinct in one and the same species). Heterocytes solitary, develop in trichomes terminally or interca- lary. (their frequency or absence is dependent on nitrogen metabolism); trichomes in principle metameric. Akinetes arise apoheterocytic, oval, little larger than cells; almost all cells between heterocytes change suc- cesively in akinetes towards heterocytes. Nostoc has special life (vegetation) cycle, during which forms several special and characteristic stages (Mollenhauer 1986, Lazaroff 1972, Komárek & Anagnostidis 1989). From several described subgenera are probably acceptable typical Nostoc and Amorphonostoc, which differ in morphology of colonies (Amorphonostoc has not periderm) and by a type of life cycle, which is more simple in Amorphonostoc.','komárek (1992)',NULL,0,0),(330,257,'description','Cells in pseudofilamentous colonies; thallus microscopic, irregular, periphytic, creeping over the substrate, with cells arranged into flat or three-dimensional groups (chroococcacean stages) or in short, irregular rows, enveloped by thin, firm, but confluent sheaths, or into pseudofilaments with irregular divarications; rows of cells uni- to two- or multiseriate, mainly with apical growth (e.g., with prevailing division of «terminal» cells). Cells irregular, polygonal-rounded in rows and especially at their ends elongate or more or less cylindrical, slight narrowed and rounded.','komárek & anagnostidis (1998)',NULL,0,0),(331,257,'description','Unicellular - colonial - pseudofilamentous; thallus microscopic,irregular, periphytic, creeping on the substrate, with cells arranged into flat or three - dimensional groups (chroococcacean stages), short, irregular rows, enveloped by thin, firm, but confluent sheaths, up into pseudofilaments with irregular branching; rows of cells uni- up to two- or multiseriate, mainly with the apical growth (= prevailing division of ˝terminal˝ cells). Cells irregular, in rows and especially at their ends elongated or more or less cylindrical, slight narrowed and rounded.','komárek (1992)',NULL,0,1),(332,259,'description','Pseudofilamentous; pseudofilaments solitary, or in small irregular groups cylindrical, isopolar, straight or slightly irregularly waved, with uniserially arranged, slightly separated one from another and in rows arranged cells within thick, homogeneous, colourless sheaths (according to original description = thickened cell-walls, 0,5-2 um wide), which are closed at both ends. Cells not motile, cylindrical, isodiametrical or longer than wide, elongated in the pseudofilament axis, enveloped probably by own gelatinous capsules (in spite of the indistinctness of sheath structures); cell content blue-green, differentiated in dark peripheral and light centroplasmic regions; in centroplasma are regularly two or three (-four) large spherical, dark blue and refractive granules,','komárek (1992)',NULL,0,0),(333,258,'description','Filamentous; filaments simple, never branched, usually in fine, smooth, layered (but not leathery) strata (mats), microscopic or (later) macroscopic up to several cm in diameter, rarely solitary or in small groups, without sheaths, only in suboptimal (extreme) conditions (or sometimes in cultures) enveloped by thin, colourless, firm sheaths, opened at the apex. Trichomes isopolar! Straight or slightly waved, usually wider than 8 μm (up over 60 μm wide), uniserial, composed of shortly cylindrical or barrel-like (discoid) cells (always shorter than wide, usually several times), constricted or unconstricted at the cross walls, not attenuated or shortly attenuated to the ends, motile under convenient environmental conditions (waving, trembling, oscillation). Cells without aerotopes but with fine granulation (sometimes prominent at the cross walls) or with solitary granules, blue-green, brownish or pinkish, with coiled thylakoids, situated usually irregularly throughout the whole cell content. End cells widely rounded, sometimes capitate or with narrow calyptra. False branching, heterocytes and akinetes absent.','komárek (1992)',NULL,0,1),(334,262,'description','Filamentous-thallous; thallus attached, heterotrichous with filaments originally creeping on the substrate, without or with very fine, colourless, unstructured and diffluent sheath (visible usually only in the upper parts of filaments). Trichomes uniseriate, flexuous, clearly constricted at cross-walls, commonly true pseudodichotomously branched, (T-, V- and indistinct reverse Y-type),towards the apices continually attenuated into the long, cellular, cylindrical, thin, hair-like ends. In the centre of old colonies arise from coalesced filaments pseudoparenchymatous flat, cellular discs with one layer of cells, adhering firmly to the substrate, from which radially arise repeatedly branched filaments, oriented_more or less parallely, free upon the substrate. Cells more or less barrel-shaped up to irregular. Heterocytes missing. Akinetes arise in short disintegrating rows, spherical or subspherical, larger than vegetative cells.','komárek (1992)',NULL,0,0),(335,263,'description','Filamentous; thallous; mats prostrate on the substrate, olive green up to blackish-green, later wooly, with densely and irregularly coiled filaments, sometimes forming erected fascicles. Filaments of different width, with very fine, narrow, colourless, thin sheaths, which are occasionally visible only at the ends of branches, sometimes with hyaline dead cells in the apical parts, resembling the sheath formation. Basal trichomes in old parts uni- or two- (rarely three-) serial, constricted at cross-walls, without visible sheaths, with common true branching of T-type. Upper parts of branches, ends of basal trichomes and young trichomes narrower than basal trichomes, uniserial, clearly constricted or not constricted at cross-walls. Cells shortly barrel-shaped or irregular-subspherical, but in some parts (particularly in branches) cylindrical, or distinctly elongated, blue-green; apical cells rounded. Heterocytes intercalar, of different shape, usually more or less cylindrical, variable in length. Akinetes arise in older parts of filaments, change from solitary vegetative cells.','komárek (1992)',NULL,0,0),(336,261,'description','Thallus attached to the substrate, hard, leathery, more or less spherical or hemispherical, often with abundant ferric precipitations, to 0.5 cm in diameter. Cells arranged irregularly within structureless, irregular mucilage and with individual gelatinous envelopes, or in irregular rows, sometimes slightly radially oriented. Cells more or less spherical or irregular.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(337,261,'description','Unicellular - colonial; thallus joined to the substrate, hard, leathery, more or less spherical or hemispherical, with common ferric precipitations, up to 0.5 cm in diameter. Cells situated irregularly within own gelatinous envelopes or in structure less mucilage, or in irregular rows, sometimes slightly radially oriented. Cells more or less spherical or irregular.','Komárek (1992)',NULL,0,0),(338,261,'description','Lager hart, lederig, kugelig bis halbkugelig, an Steinen festgewachsen, bis 0,5 cm groß, mit Eisen imprägniert. Zellen in gemeinsamer Gallerte in Radialen Reihen bzw. Gallertfäden angeordnet.','Geitler (1932)',NULL,0,1),(339,264,'description','Pseudofilaments of «connected» cells solitary, uniseriate, more or less cylindrical, heteropolar, more or less erect, without wide mucilaginous envelopes, attached by one end (with modified basal, usually ovoid cell with narrowed basal stipe) to the substrate. Cells in pseudofilaments more or less of the same size and shape, rounded or barrel-shaped (causing the moniliform appearance of pseudofilaments), only the basal cell is modified and the terminal cell(s) slightly enlarged and usually elongate-rounded, but not exceeding distinctly the pseudofilament width. Around cells narrow, firm sheaths, visible only during cell division or after baeocyte liberation.','komárek & anagnostidis (1998)',NULL,0,0),(340,264,'description','Pseudofilamentous; pseudofilaments solitary, isolated, moniliform, uniserial, heteropolar, composed from more or less elongated basal cells joined to the substrate by narrow and shortly elongated end, and from a row of spherical, barrel-shaped or obovate cells, which arise probably by the successive and repeated crosswise cell division; apical cell usually elongated, cylindrical and rounded. Without gelatinous sheath, but at the apex, where the cells divide into nanocytes (7), occurs very narrow, firm, colourless sheath. Cells with pale blue-green content.','komárek (1992)',NULL,0,1),(341,265,'description','Filaments free, usually solitary or in small groups, slightly coiled, creeping on the substrate or a little erected, heteropolar, with morphologically separated base (sometimes with a heterocyte) and free apical end, with false branching (branches lateral, solitary or in pairs, dividing after the disintegration of trichomes at heterocytes). Sheaths firm, very thick, distinctly funnel-like, lamellated, colourless or yellow-brown, limited from outside. Trichomes cylindrical in basal and middle parts, with elongated, cylindrical or barrel-shaped cells; in terminal parts are cells shorter, barrel-shaped and usually widened; apical cells always rounded. Heterocytes intercalar, solitary, more or less spherical and usually wider than vegetative cells. Akinetes missing.','komárek (1992)',NULL,0,0),(342,266,'description','','Komárek & Hauer orig.',NULL,0,0),(343,267,'description','Filamentous; filaments unbranched, rarely solitary, usually in fine, smooth, layered up to leathery strata (mats), microscopic and later macroscopic up to several cm in diameter, usually covering substrates of different types. Sheaths develop facultatively in different frequencies, only in suboptimal conditions (subg. Gomontinema), in dependence on changing environmental factors (subg. Phormidium), or regularly in all conditions (with exceptionally living free trichomes - subg. Hansgirgia); sheaths are tube-like, firm, colourless, joined to the trichomes, not layered, opened at the ends, containing always only one trichome. Trichomes isopolar, more or less straight, coiled or waved, usually 2-12(14) μm wide, uniserial, never branched, composed of cylindrical up to slightly barrel-shaped cells, more or less isodiametrical or slightly shorter or longer than wide, constricted or unconstricted at the cross walls, not attenuated and bent or screw-like twisted towards the ends, motile (waving, creeping, oscillations) within and out of sheaths. Cells without aerotopes or exceptionally with aerotopes under special, suboptimal conditions (but never characteristic of planktic<br> species), sometimes with granular content or with prominent granules spread throughout the cell volume, or agglomerated at the cross walls; end cells widely rounded, attenuated or pointed, sometimes with calyptra. Cell content usually blue-green, rarely brownish, pinkish or violet, sometimes modifications with stable PE:PC ratio occur; thylakoids situated perpendicularly to the cell wall (radially in a cross section). Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(344,260,'description','Colonies microscopic, free floating, hollow, in young stages irregularly spherical with holes, later more irregular in outline, flattened, wavy or hemispherical, arcuate, clathrate or composed of subcolonies, in old stages usually elongate and lobate, with one to three layers of more or less radially or irregularly, densely distributed cells. Around colonies fine, colourless, homogeneous, watery (diffluent at the margin) mucilage. Cells spherical, with or without gas vesicles (two different genera?).','komárek & anagnostidis (1998)',NULL,0,0),(345,260,'description','Unicellular, colonial; colonies free-floating or mixed with-other algae 1 and among water plants, microscopic, flattened, irregular in outline, clathrate and waved, composed of subcolonies, with cells situated irregularly in one plane, in a layer of 1-3; young colonies more or less spherical, old colonies irregular, many-celled. Colonial mucilage fine, homogeneous, colourless, diffluent. Cells spherical or slightly elongated (before division), after division hemispherical, pale blue-green, with or without gas vesicles, sometimes surrounded with special fine, diffluent mucilaginous envelopes.','komárek (1992)',NULL,0,1),(346,270,'description','Filamentous; filaments solitary, with thin, simple, colourless, but firm sheaths, very exceptionally with false branching; trichomes cylindrical, isopolar, straight, waved, coiled up to more or less screw-like or spirally coiled, narrow, up to 3 μm wide, uniserial, usually not narrowed to the ends, indistinctly constricted or unconstricted at the cross walls, always immotile. Cells cylindrical, rarely shorter than wide, usually longer than wide (up to several times), without aerotopes or with facultative polar aerotopes, some- times with solitary granules; end cells rounded or narrowed-rounded, always without calyptra. Cell content pale grey-blue, blue-green, yellowish or olive-green, thylakoids localized peripherally along the cell walls.','komárek (1992)',NULL,0,0),(347,271,'description','The trichomes are solitary, float, are generally straight, or slightly bent near the apex and attenuated toward their ends. Occasionally, a very thin, clear sheath is observed. Cross walls are slightly constricted, or not constricted and not granulated. Many small gas vacuoles are scattered at the periphery of the cells and they are easily ruptured during observation with a light microscope when the cover slip is placed on a drop of culture. It has no phycoerythrin and no capacity<br> to undergo complementary chromatic adaptation. Fatty acid composition is Type 4. DNA base composition is about 44 mole % GC. This species forms a independent phylogenetic cluster from Planktothrix based on 168 rDNA sequence analysis. The type species of this genus is Planktothricoides raciborskii. The genus description is based on the data cited above.','Suda et al. (2002)',NULL,0,0),(348,268,'description','Cells in more or less globular colonies, located near the surface of gelatinous, irregular spheres; thallus is small or expanded, mucilaginous, more or less lobate or vesiculose with wavy or smooth surface, usually «hollow», with cells situated in one or several layers in the outer part of the colony, irregularly or radially arranged in irregular rows or groups, or in flattened layers. Gelatinous envelopes colourless, yellow-brownish or pinkish coloured. Cells without or with individual envelopes, which are sometimes layered, more or less spherical, irregular in outline or slightly elongate, with homogeneous, blue-green, olive-green, yellow-green or pinkish, sometimes slightly granular content.','Komárek &amp; Anagnostidis (1998, sub Placoma)',NULL,0,0),(349,268,'description','Unicellular - colonial; thallus small or expanded, gelatinous, more or less spherical, irregular spherical, slightly lobate or vesiculose with waved surface, usually hollow, with cells situated in one or several layers on the surface of a colony, irregularly, radially or in irregular rows or groups. Gelatinous envelopes colourless, yellow-brownish or pinkish coloured. Cells with or without special own envelopes, sometimes layered, more or less spherical, irregular in outline or slightly elongated, with homogeneous, blue-green, olive-green, yellow-green or pinkish, sometimes slightly granular content.','komárek (1992)',NULL,0,1),(350,268,'description','Lager halbkugelig oder unregelmäßig-gekröseartig, gefaltet, lappig, im Alter im Innern hohl, weit ausgebreitete Überzüge bildend. Zellen in weiten blasigen Hüllen, nach Art von Gloeocapsa in Zellfamilien, welche an der Peripherie des Lagers<br> mehr oder weniger deutlich radial orientiert sind.','Geitler (1932)',NULL,0,1),(351,272,'description','Filaments solitary, rarely in small irregular and easy disintegrating fascicles (groups) (in the mass developments), more or less straight or slightly waved, isopolar, free living; usually growing without sheath. Sheaths occur facultatively in several species, in typical planktic species only under unfavourable conditions; they are fine, thin, colourless, joined to the trichome, opened at the apex. Trichomes with cylindrical; cells, slightly constricted at the cross walls, sometimes slightly tapering to the ends, up to 4 mm long, 3.5-10 um wide; occasionally with slight movement (trembling).Cells slightly shorter than wide up to +/- isodiametric, rarely Slightly longer than wide, with aerotopes through the whole cell volume (but sometimes without gas vesicles in parts of trichomes); end cells (when fully developed) widely rounded or slightly narrowed and with thickened outer cell wall or with calyptra. Without chromatic adaptation, with +/- constant phycobilin ratios. Presence of carotenoids myxoxanthophyll and oxillaxanthin. False branching, heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(352,269,'description','Cells rarely solitary or in couples, mostly in random groups, forming irregular dense expanded aggregations. Colonies microscopic, free, irregular, to 100 um in diameter, composed of joined solitary cells, not covered by common mucilaginous envelopes.<br> Cells cyanoprokaryotic, spherical, (0.8)-1-1.8 μm in diameter, blue-green to pale blue-green in colour; aerotopes (pseudovacuoles) missing. Mucilage of cells wide, firm, spherical, hyaline, 4-6 μm wide, bilamellate, composed of an inner light spherical part and an outer darker part with a distinct margin.','Hindák (2002; for type species)',NULL,0,0),(353,274,'description','Thallus creeping on the substrate (mainly on stones), crustose, in a thin layer or in three-dimensional clusters, composed of irregular groups of cells (chroococcacean stages), from which irregular or radial rows of cells grow, sometimes irregularly and pseudodichotomously branched; in several species the pseudofllaments are partly endolithic. Rows of cells uni- or multiseriate, enveloped by more or less thin, firm, sometimes lamellate and yellowish-brownish coloured sheaths which are laterally confluent. Cells irregular, of variable size, sometimes (in pseudofilaments) slightly elongate, with homogeneous or slightly granular content, sometimes with several prominent granules, blue-green, pale blue-green or pinkish.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(354,274,'description','Unicellular - pseudofilamentous; thallus creeping on the substrate (mainly on stones), crust-like or in a thin layer, composed from irregular groups of cells (chroococcacean state), from which grow irregularly or radially rows of cells, sometimes irregularly branched; in several species are the pseudofilaments endolithic; rows of cells uni- or multicellular, enveloped by more or less thin, firm, sometimes lamellated and yellowish-brownish coloured sheaths, which confluent together by their sides. Cells irregular, of different size, sometimes (in pseudofilaments) slightly elongated, with homogeneous or slightly granular content, sometimes with several prominent granules, blue- green, pale blue-green or pinkish.','komárek (1992)',NULL,0,1),(355,273,'description','Filamentous; filaments long, isopolar, solitary or in macroscopic clusters, usually waved or coiled, always with more or less thick, firm, colourless sheaths, sometimes slightly lamellated, open at the apex, obligatory and frequently falsely branched. Trichomes isopo1ar, 8-25 μm wide, uniserial, composed of shortly cylindrical or barrel-like (discoid) cells (always shorter than wide, usually several times), constricted or unconstricted at the cross walls, not attenuated or very shortly attenuated towards the ends, immotile (with exception of hormogonia). Cells without aerotopes, sometimes with granular, blue-green, olive-green or grey-blue content; end cells widely rounded, sometimes capitate or with slightly thickened outer cell wall. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(356,275,'description','Thallus epilithic, granular, thin, irregularly covering the substrate, composed of more or less erect or aggregated, more or less parallel or irregular rows of several separate cells (up to 4-6), which are polarized, narrowed towards the basal end and wider in the upper part. «Terminal» cells irregular spherical, ellipsoidal, pear - shaped, drop-like or club-shaped; the short rows of cells sometimes pseudodichotomously divaricate, enveloped by thick, firm, layered and coloured sheaths.','komárek & anagnostidis (1998)',NULL,0,0),(357,275,'description','Unicellular - colonial; thallus epilithic, granular, thin, irregularly covering the substrate, composed from more or less erected or agglomerated, more or less parallel rows of several separated cells (up to 4-6), which are polarized, narrowed towards the ˝basal end and more widened in the upper part, ˝terminal˝ cells sometimes irregular spherical, pear-shaped, drop-like or club-shaped; the short rows of cells sometimes pseudodichotomously or pseudotetrachotomously divaricated, enveloped by thick, firm, layered sheaths. Cells pale blue-green, with more or less homogeneous content.','komárek (1992)',NULL,0,1),(358,278,'description','Marine planktonic cyanobacteria that possess spherical to slightly rod-shaped cells (0.5-0.8 X 0.7-1.6 um) and divide by binary fission in a single plane. They lack phycobilisomes and contain divinyl-chlorophyll a and b (a2 and b2). The members of this genus (Fig. BIO.22) range in size from 0.5 to 0.8 um in width and 1.0-1.6 um in length (predivisional cells). Although they show a superficial resemblance to various slightlv larger strains of picoplanktonic marine Ssnechococcus (see Fig. B10.24F), all isolates of Prochlorococcus are distinguished by their lack of phycobilisomes and phycobiliproteins (except small quantities of PE III in the case of strain CCMP 1375T; see Hess et al.,1999. and possibly other strains). As a light-harvesting-antenna members of the genus Prochlorococcus synthesize divinyl-chlorophyll a and b (a2 and b2) (Goericke and Repeta, 1993). Thi the principal characteristic distinguishing this genus is the replacement of phycobilisomes bv a chlorophyll a/b complex analogous to that of green algal and green plant chloroplasts. This pigment composition confers a yellow-green color to the culture.','Castenholz (2001)',NULL,0,1),(359,277,'description','Filamentous; filaments unbranched, usually slightly coiled, solitary or in microscopic up to macroscopic clusters or compact mats, always with sheaths (only escaped hormogonia and germinating hormogonia without sheaths). Sheaths firm, thick, later always layered, tube-like, joined to the trichomes or slightly distant from them, colourless or coloured with yellow-brown or reddish sheath-pigments (intensity of ´colouration´ is dependent on the environmental conditions, type of colouration is species-specific), open at the apex, containing one, very rarely two parallel trichomes; sheaths are often characteristically widened and coiled after hormogonia release. Trichomes isopolar ,6-20 um wide, cylindrical, with or without constrictions at the cross walls, immotile (hormogonia motile ?). Cells isodiametrical or slightly longer or shorter than wide, without aerotopes, sometimes with granular content or several prominent granules; end cells widely rounded, sometimes with thickened outer cell wall. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(360,279,'description','Division. Prochlorophyta (Lewin, 1976). Prokaryotic algae resembling cyanophytes, from which they differ in<br> that they form chlorophylls a and b and lack accessory red or blue bilin pigments. Class. Prochlorophyceae. With the characters of the division.<br> Order. Prochlorales. Unicellular or filamentous, branched or unbranched.<br> Family. Prochloraceae. Unicellular, encapsulated or not.<br> Genus. <i>Prochloron</i>. Unicellular, spherical, without evident mucilaginous sheath. Only form of reproduction so far observed: binary division, by equatorial constriction. So far, only found as extracellular symbionts of ascidians on marine shores.','Lewin (1977)',NULL,0,0),(361,282,'description','Filamentous; filaments (trichomes) solitary or agglomerated in very fine, mucilaginous mats, straight or slightly waved or arcuated, simple, usually ; not very long, without any branching, 0.8-3 um wide, composed from cylinidrical cells, usually with slight constrictions at the distinct cross walls; only in young trichomes are the cross walls thin and unclear, without firm sheaths, sometimes with fine, colourless, diffluent, narrow mucilagi- nous envelopes (staining); ends of trichomes not attenuated, but the apical cell is sometimes conical; indistinct and facultative motility (trembling). Cells cylindrical, always longer than wide, without aerotopes, but sometimes with solitary granules (subg. Pseudanabaena, Skujanema) , or with gas vesicles agglomerated into aerotopes, localized in the ends of cells (in polar positions) (subg. Ilyonema), thylakoids localized parallely, peripherally; special pore patterns on the cell walls; end cell cylindrical and rounded at the end (subg. Pseudanabaena), or more or less conical up to bluntly or sharply pointed (subg. Skujanema, Ilyonema).','komárek (1992)',NULL,0,0),(362,285,'description','Filamentous; filaments solitary, joined into microscopic or macroscopic clusters or mats (strata) covering the substrate, obligatory with firm, irregularly tube-like, colourless sheaths, commonly and intensely irregularly falsely branched, sometimes with two parallel trichomes in a sheath. Trichomes often fragmentated,. cyrrndical, isopolar; usually short, irregularly curved and coiled, 1-18 um wide, uniserial, composed of barrel-shaped or cylindrical cells, constricted or unconstricted at cross walls, not attenuated or slightly attenuated to the ends, immotile. Cells isodiametrical or slightly longer or shorter than wide, without aerotopes, but usually irregularly granulated or with several prominent granules, blue-green, greyish blue-green or pinkish; end cells rounded or conical-rounded, sometimes with thickened outer cell wall. Heterocytes and akinetes absent.','komárek (1992)',NULL,0,0),(363,286,'description','Filaments rarely solitary, mainly in clusters or fine mats, isopolar, composed from a trichome with both widened ends and from a simple, firm, colourless, thin sheath, opened at the apex. Trichomes z long, uniserial, curved or flexuous, isopolar, composed from cylindrical or slightly barrel-shaped cells, which are usually longer than wide, unconstricted or constricted at the cross walls; they are shorter and wider towards the ends and the constrictions become deeper, the end cell is widely rounded or almost spherical; trichomes clearly widened at both ends. False branching rare up to common, one or two lateral branches develop after the trichome division between two vegetative cells (necridic cells ?). Cells without aerotopes, but often with solitary granules or granules near the cross walls, often vacuolized at the ends; end cells contain usually one large vacuole. Heterocytes and akinetes lacking.','komárek (1992)',NULL,0,0),(364,281,'description','Filamentous; filaments relatively short, solitary, composed from cylindrical trichomes, slightly narrowed to the ends, not constricted at the cross walls, and wide, colourless sheaths, usually irregularly swollen and wavy on the surface; filaments grow endophytically within sheaths of other filamentous cyanophytes or epiphytically, creeping on their surface. Cells more or less isodiametrical or slightly longer or shorter than wide, end cells conical-rounded.','komárek (1992)','[281]',0,0),(365,287,'description','Thallous; thallus microscopic, attached to the substrate, composed from more or less circular, discoidal, basal layer of cells with nematoparenchymatous arrangement of radially oriented, laterally confluent filaments, later slightly hemispherical; from the basal disc grow parallely and radially oriented filaments with laterally confluent sheaths. Trichomes uniserial or biserial in short segments, pseudodichotomously divaricated at the ends (branching of V-type). Sheaths more or less thick, homogeneous or indistinctly layered, colourless or yellowish, confluent. Cells rounded-irregular, blue-green. Heterocytes interca1ar, solitary. Akinetes not observed.','komárek (1992)',NULL,0,0),(366,288,'description','Thallus at first in the form of a flat, discoidal or irregular, nemato- or blastoparenchymatous colony (these stages rarely lacking), attached to the substrate, from which more or less erect, short, parallely arranged, straight or slightly curved, simple or sometimes pseudodichotomously divaricate, uniseriate or multiseriate rows of cells (pseudofilaments) arise. Mucilaginous sheaths around pseudofilaments confluent, forming later homogeneous mucilage; old colonies m the form of a narrow, flat, gelatinous or crustose layer with parallely arranged pseudofilaments, oriented perpendicularly to the substrate. Cells more or less irregular- polyhedral-rounded, at the ends of pseudofilaments enlarged; the apical cells, dividing later into baeocytes, are therefore larger than vegetative cells and develop terminally or subterminally, on the top of pseudofilaments, i. e., near the surface of flat colonies.','komárek & anagnostidis (1998)',NULL,0,0),(367,288,'description','Unicellular - colonial - pseudofilamentous; thallus crust-like, composed from more or less erect, parallel situated pseudofilaments; cells situated in irregular, mono- or multilayered rows, enveloped by firm gelatinous sheaths, which confluent by their sides together. Cells more or less irregular polyhedral, at the ends of erect pseudofilaments enlarged.','komárek (1992)',NULL,0,1),(368,289,'description','Colonies free floating, more or less spherical to irregular, microscopic, with fine, colourless, diffluent gelatinous envelopes, with cells more or less irregularly grouped in the colonial center and radiating in all directions in more or less uniseriate rows; cells in radial rows slightly distant from one another or (after division) in pairs, widely oval or almost spherical, facultatively with aerotopes.','komárek & anagnostidis (1998)',NULL,0,0),(369,289,'description','Unicellular - colonial; colonies more or less spherical or slightly irregularly oval, microscopic, up to 100 μm in diameter, free-living, enveloped by very fine, colourless and diffluent gelatinous mucilage, with more or less radially oriented cells in short, variable rows, which are usually slightly disordered; cells separated slightly one from another, sometimes in pairs (after division). In the centre of colony and in old colonies are sometimes the rows of cells not clearly distinct. Cells spherical up to widely oval (particularly before division), with pale blue-green content, sometimes with scarcely occurring aerotopes.','komárek (1992)',NULL,0,1),(370,290,'description','Trichomes solitary, free floating, without sheaths and gelatinous envelopes, straight, waved or screw-like coiled, isopolar, uniserial, usually slightly attenuated toward both ends (or to one end after trichome disintegration), but not elongated in cellular hair-like ends, constricted at cross-walls. Cells barrel-shaped, sometimes slightly elongated to the ends, facultatively with gas vesicles (aggregated in aerotopes); apical cells conical-rounded or pointed. Heterocytes missing. Akinetes develop in the middle of trichomes in series.','komárek (1992)',NULL,0,1),(371,291,'description','Differing from all genera in the Microchaetaceae by cell division in two planes. Filaments falsely<br> branching, with one or more trichomes per filament. Trichomes isopolar. Hormogonia one to few celled, capable of undergoing division in two planes.','casamatta et al. (2006)',NULL,0,0),(372,293,'description','Fusiform cells are arranged irregularly, distant, rarely more or less in one direction, in microscopic mucilaginous colonies. Mucilage is fine, homogeneous, colorless, and usually diffuse or indistinct at the margin. Cells are fusiform or cylindrical with conical cell ends, sometimes pointed, often slightly curved, (1.8)3-12(22) X (0.5)1-3.5(6) μm, with pale blue-green or olive-green content. Involution filamentous cells are up to more than 25 μm long (known only from culture). Cell division is by binary fission, transverse to the long axis into two more or less isomorphic daughter cells. Reproduction is by disintegration of colonies','Komárek (2003)',NULL,0,0),(373,293,'description','Colonies mucilaginous, microscopic (rarely macroscopic), irregular, usually free-floating, with cells distant from one another, situated irregularly (more or less parallel in young colonies) in fine, diffluent (rarely limited), colourless, structureless mucilage; number of cells usually small<br> (sometimes only 1-3 cells in a colony). Cells elongate, narrow, spindle-shaped, ellipsoidal or more or less cylindrical with short attenuate and acute or acute-rounded<br> poles, without aerotopes, straight or slightly arcuate or sigmoidally coiled; around the cells or their small groups thereof sometimes a fine individual, homogeneous envelope. In cultures (R. smithii/ellipsoidea) pseudofilamentous formations and filamentous involution cells (like in Synechococcus) often with asymmetrical cell division.','Komárek & Anagnostidis (1998)',NULL,0,0),(374,293,'description','Unicellular - colonial; colonies microscopic, containing relatively small number of cells, mucilaginous, with more or less elongated cells, disposed freely, distant one from another, sometimes oriented more or less in one direction; colonial slime colourless, without structure or very finely and indistinctly, irregularly concentrically lamellated, fine, sometimes diffluent at the margin. Sometimes few small colonies clustered together. Cells spindle-like, narrowed to both ends, pointed, rounded-pointed or narrowed-rounded, straight or curved, with pale blue-green or grey-blue, homogeneous content. Involution cells filament-like.','Komárek (1992)',NULL,0,0),(375,293,'description','Zellen zylindrisch und an den Enden zugespitzt, oder spindelförmig, oder ellipsoidisch und zugespitzt, gerade oder mehr oder weniger spiralig, S-förmig oder unregelmäßig gekrümmt, selten einzellen, meist zu wenigen in zarter, schwer sichtbarer Gallerte zu Kolonien vereinigt. Teilung quer.','Geitler (1932; sub <i>Dactylococcopsis</i>, incl. <i>Myxobaktron</i>)',NULL,0,0),(376,292,'description','Cells in small microscopic, irregularly oval or elongate-irregular mucilaginous colonies, usually distant from one another or in short pseudofilamentous rows, irregularly and widely spaced, but often oriented in one direction in a colony. Mucilage fine, colourless, homogeneous, sometimes diffluent (staining !); cells rarely with individual fine, indistinct gelatinous envelopes. Cells cylindrical, rod- shaped, straight, arcuate or sigmoid, with rounded ends, sometimes several times longer than wide; occasionally are present long, filamentous involution cells or unevenly long cells in one colony.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(377,292,'description','Unicellular - colonial; colonies microscopic, containing usually relatively small number of cells, only old colonies rarely with many cells, mucilaginous, with more or less elongated cells, loosely arranged, distant one from another, oriented more or less in one direction or in loose rows (this position is disturbed in old colonies); colonial slime colourless, without structure, homogeneous and usually diffluent at the margin. Sometimes few small colonies clustered together. Cells long oval up to rod-like, rounded at the ends, straight, arcuated or sigmoid, with pale blue-green, rarely pinkish homogeneous content. Involution cells filament-like.','komárek (1992)',NULL,0,1),(378,292,'description','Zellen länglich-ellipsoidisch bis zylindrisch, gerade oder halbkreisförmig bis S-förmig gekrümmt, in gemeinsamer, meist schwer sichtbarer homogener Gallerte zu wenigen beisammen. Kolonien flach-hautartig oder rundlich. Zellen einzeln oder nach der Teilung zu zwei bis mehreren in Reihen. Teilung quer.','Geitler (1932)',NULL,0,0),(379,294,'description','Colonies widely spreading, consisting of one layer of erect, parallely and more or less densely arranged rows of cells, vertically oriented to the substrate and enveloped by common, fine mucilage and indistinct mucilaginous tube-like envelopes; cells in rows, slightly distant from one another, uniseriately organized one after another or (in Short sections) oriented at right angles to the row. Mucilage in the basal parts of colonies more dense than elsewhere (there it forms an irregular net-like structure, seen from above), in the upper parts fine, homogeneous. Cells cylindrical, with rounded poles (never spindle-shaped).','komárek & anagnostidis (1998)',NULL,0,0),(380,294,'description','Pseudofilamentous - colonial; colonies in form of wide, macroscopic, encrusted layers, dark purple up to reddish black, up. to 50 μm thick, composed from erected, parallely disposed rows of cells enveloped by fine, colourless gelatinous envelopes, only at bases distinctly limited, con- fluent by their sides. Cells rod-like, cylindrical, rounded at the ends, sometimes slightly curved, by their longer axis oriented to the surface of the colony (lying in the ˝axis of the row of cells), or<br> secondary perpendicularly to it. Cells with pale pink content, in more layers reddish. The reddish colour of the colony is caused by the colour of cells, not of mucilage.','komárek (1992)',NULL,0,1),(381,283,'description','Colonies spherical or irregularly packet-like, in aggregates, microscopic (aggregates often of macroscopic size), with radially or fan-like oriented, later irregularly, densely aggregated cells; colonies enveloped by thin, firm, smooth, colourless, sometimes striated sheaths; often composed of subcolonies. Cells irregular spherical, after division hemispherical, later irregular or in the form of  segments of a sphere, more or less radially oriented in the colonies; in old colonies the cells are densely and irregularly aggregated.','komárek & anagnostidis (1998)',NULL,0,0),(382,283,'description','Unicellular - colonial; initial cells spherical, later hemispherical up to irregularly rounded-conical, packed into colonies; colonies are in a form of 2-16-celled up to multicelled packet-like aggregates with tightly, radially and ˝fan-like˝ oriented cells (with the ˝conical˝ part oriented into the centre of a colony), enveloped by a thin, colourless, usually firm, tight and sometimes slightly structured (lamellated) gelatinous envelope (the outer layers of which in several species gelatinate m. and become to be diffluent). Cells blue-green, pale greyish blue-green or yellowish and olive-green, sometimes with several prominent granules in plasma or with finely granular content.','komárek (1992)',NULL,0,0),(383,280,'description','Prochlorothrix is a filamentous organism that divides exclusively by binary fission in one plane and has slight to prominent constrictions at the cross-walls. Cells are longer (3-10 μm) than broad (0.5-1.5 μm in diameter). However, under salt stress (i.e., 25 mM NaCl) cells may<br> enlarge to reach 15 μm in length and 3 μm in width. Thylakoids arranged in layers parallel to the long axis at the periphery of the cytoplasm. Phycobilisomes absent. Motility absent; polar gas vacuoles present; sheaths absent or poorly developed; apical cells undifferentiated (rounded). LacksN2-fixing ability. Phycobiliproteins (i.e., CPE, C-PC,<br> and APC) absent; chlorophyll a and chlorophyll b present. Zeaxanthin and β-carotene are the major carotenoids.','Castenholz (2001)',NULL,0,0),(384,284,'description','Colonies ucilaginous, more or less polarized, attached to stony substrates, gelatinous, more or less hemispherical or flattened, (to 2 or more mm high), with cells situated in distinctly «branched», divaricate, radially or vertically oriented rows, enveloped by gelatinous, tubular and confluent sheaths, and, moreover, cells with individual spherical, distinct, delimited or diffluent, non-stratified envelopes (staining !). The whole colony is embedded in homogeneous mucilage with distinct margin. Cells more or less spherical, ellipsoidal or cylindrical with rounded ends, sometimes up to 25 um long.','komárek & anagnostidis (1998)',NULL,0,0),(385,284,'description','Unicellular - colonial; thallus joined to the stony substrate, gelatinous, more or less hemispherical or flattened (up to 2 mm in diameter), with cells, situated in distinct ˝branched˝, radially or vertically oriented rows, enveloped by gelatinous tubular and confluent envelopes and, moreover, by own spherical but not layered envelopes, which are distinct or more or less diffluent. The whole colony is embedded by homogeneous, limited mucilage. Cells large (up to 25 /um long), ellipsoidal<br> up to shortly cylindrical cells with rounded ends, with slightly granular content.','komárek (1992)',NULL,0,1),(386,284,'description','Zellen ellipsoidisch bis zylindrisch, mit nicht ineinander geschachtelten, distinkten oder zerfließenden Spezialhüllen, in gemeinsamer homogener Gallerte liegend, zu deutlichen, mitunter verzweigten Reihen angeordnet, halbkugelige oder flache festsitzende<br> Lager bildend.','Geitler (1932)',NULL,0,0),(387,297,'description','Generic phenotype characters:<br>- Trichomes free-living, solitary, or few in irregular mucilaginous clusters.<br>- Trichomes short, usually (l)2-12(23)-celled, exceptionally with more (up to &gt;60) cells, frequently fragmentation.<br>- Trichomes usually irregularly wavy or coiled, rarely almost straight, or irregularly screw- like , 0.6-3 um wide.<br>- Trichomes constricted at cross-walls (species without constrictions belong probably to other genera (genotypes); it concerns particularly<em>&nbsp;R. austriaca</em> and <em>R. cryophila</em>. Characteristical is the occasional shift of neighbouring cells within trichomes.<br>- Trichomes enveloped by fine, colourless, diffuse mucilaginous envelopes (in all species?). Sheaths are lacking.<br>- Cell cylindrical, always longer than wide. In few species the Y-shaped cells were found.<br>- Cell division cross-wise, sometimes asymmetrical. Heterocellular trichomes occur.<br>- Terminal cells do not differ from other cells, capable to divide.<br>- Thylakoids arranged parietally in cylindrical cells.<br>- Cell connected by gelatinous matrix of various width; pores in connecting cross-walls are lacking (always?).<br>- Gas vesicles lacking.<br>- Reproduction by trichome fragmentation.','Komárek (2001: 6-7)','[322]',0,0),(388,297,'description','Filamentous and pseudofilamentous; trichomes solitary or rarely in microscopic colonies, free-floating, fine, few-celled, disintegrating up to solitary cells, unbranched, irregularly up to screw-like coiled, with sometimes freely connected cells by their ends, enveloped usually by very fine, diffluent, colourless, slightly visible mucilaginous envelopes (staining !), always without sheaths, isopolar, 0.6-3 um wide, constricted at the cross walls, not attenuated at the ends, immotile. Cells elongated, cylindrical, always longer than wide (usually several times), cut or rounded at the ends, without aerotopes; end cells cut or rounded, without thickened cell walls or calyptras. Cell content pale blue-green, greyish or yellowish, usually homogeneous, thylakoids localized peripherally (as known). Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(389,297,'description','Cells joined in free floating, isopolar, bent, circular to coiled pseudofilaments embedded in hyaline mucilaginous envelopes, without motion; cells without gas vesicles;cell division by binary fission in two equal parts; without nanocytes and involution cells.','Hindák (1988: 293-294)',NULL,0,1),(390,297,'description','Le genre Romeria Koczwara in Geitler, 1932, Rabenhorst´s Kryptogamenfîora (= <i>Raciborskia</i> Koczw. 1928, Kosmos, 53 = Amalia J. De Toni 1934) (PI. 80, flg. 6 à 8) montre des filaments libres solitaires, très courts, formés d´un petit nombre de cellules (1 à 16 mais le plus souvent 4) contour- nés irrégulièrement en C, en S. Il n´y a pas<br> de gaine visible et les cellules sont assez allongées, rétrécies au niveau des cloisons. Chez une espèce on observe une auréole muqueuse très diffluente. Il s´agit toujours de filaments très étroits (1 à 2 y de diamètre), très peu colorés. Nous avons examiné l´échantillon-type distribué par raciborski sous le nom de <i>Arthrospira leopoliensis</i> dans la Phycotheca Poloniae, n° 9. La teinte de ces minuscules trichomes desséchés depuis des années (1909) est si pâle qu´il est impossible de savoir s´il s´agit d´une Cyanophycée ou d´une Bactérie. Récemment claus (1961,Int. Rev. Ges. Hydrobiol. 46, 4) a décrit une espèce nouvelle qui montre des cellules non rétrécies aux cloisons, qui se déplace comme les Spirulines mais plus lentement et qui est peut-être un Borzia (voir Komárek, 1969, - in lit.l.c.).','Bourrelly (1970: 309)',NULL,0,1),(391,297,'description','','Kondrateva (1968: 74)','[325]',0,1),(392,297,'description','Trychomy pojedyncze, krótkie, l—8—(16)-komórkowe, skręcone półkulisto lub spiralnie (l—2 skręty spirali), bez pochwy, lecz u jednego gatunku z delikatną osłoną galaretowatą, przy ściankach poprzecznych wcięte. Komórki podłużnie cylindryczne, na końcach zaokrąglone. Istnieje pewne podobieństwo do rodzaju <i>Rhabdoderma</i>.','Starmach (1966: 364)',NULL,0,1),(393,297,'description','Kommt entweder in einzelnen Fäden oder kleinen Kolonien vor, die aus einigen kurzen Fäden zusammengesetzt und mit ihren Enden mittels Schleim verbunden sind. Die Gallerte fehlt oder ist farblos, sehr undeutlich, zerfliessend und bildet um die Trichome herum breite Hüllen. Die Fäden sind selten gerade, in der Regel unregelmässig „S˝-förmig oder kreisförmig gebogen, der ganzen Länge nach gleich breit, mit abgerundeten Endzellen; an den Querwänden ist manchmal eine Einschnürung bemerkbar. Heterocysten und Arthrosporen fehlen. Die Zellen sind zylindrisch und teilen sich senkrecht zur Achse des Trichoms. Vermehrung: durch Teilung der Trichome und event. durch den Zerfall der Kolonie im Laufe der Vegetationsperiode, zuletzt durch völligen Zerfall in einzelne Zellen.','Komárek (1958: 159-160)',NULL,0,1),(394,297,'description','','Hollerbach et al. (1953: 466)','[308]',0,1),(395,297,'description','The trichomes of <i>Romeria</i> are short, curved to spirally twisted, and rarely with more than a dozen uniseriately arranged cells. There may or may not be an evident gelatinous sheath external to a trichome. The cells are cylindrical, with more or less broadly rounded poles, and with a length twice to several times the breadth.Heterocysts and akinetes are never formed, and reproduction is by fragmentation of trichomes.','Smith (1950: 575)',NULL,0,1),(396,297,'description','','Elenkin (1949: 1427)','[314]',0,1),(397,297,'description','Trichome einzeln, sehr kurz, ein- bis acht- (bis sechszehn-) zellig, halbkreisförmig oder schraubig gebogen mit l - 2 Umgängen, scheidenlos (bei einer Art mit Gallerthülle), an den Quer- wänden eingeschnürt. Zellen lang zylindrisch, an den Enden abgerundet. Nach dem polnischen Geographen E. Romer benannt.-Vermutlich gehört hierher auch <i>Spirulina okensis</i> (C. Meyer) Geitl.(= <i>Arthrospira okensis</i> C.Meyer, Arbeiten Oka-Station, 1926, 40, Fig. 2).','Geitler(1942: 217)',NULL,0,1),(398,297,'description','Trichome einzeln, sehr kurz, 1-8 (-16) zellig, halbkreisförmig oder schraubig gebogen, mit l bis 2 Umgängen, scheidenlos (bei einer Art mit Gallerthülle), an den Querwänden eingeschnürt. Zellen lang-zylindrisch, an den Enden abgerundet.','Geitler (1932: 915)',NULL,0,1),(399,297,'description','Nici krótkie, 1—8 (16) komórkowe, najczęściej 4 - r o komórkowe, łukowato<br> lub e s o w a t o zgięte, częściowo zwinięte spiralnie. Spirale albo niepełne, albo tworzą l, rzadko 2 niezupełne zwoje; zwoje luźne, szerokie i nieregularne. Komórki dłuższe niż szerokie, walcowate, na końcach zaokrąglone lub spłaszczone, od siebie wyraźnie oddzielone. Występują wplanktonie stawów, tworząc czasami zakwit.','Koczwara (1929: 107, sub <i>Raciborskia</i>)',NULL,0,1),(400,296,'description','Filaments heteropolar, differentiated into basal and apical parts, simple, joined parallely into firm, at the beginning of the vegetation cycle hemispherical or spherical, later sometimes vaste, flat, macroscopic, irregular strata, up to several cm or dm in diameter and several mm thick; strata are layered (sometimes with several layers), with densely agglomerated trichomes, oriented by their bases with heterocytes to the substrate and by the apical hair-like parts to the surface of the colony. Strata are gelatinous up to leathery or intensely incrusted by calcium carbonate, always covering the substrate. Trichomes +/- cylindrical, constricted or unconstricted at the cross walls, dividing at intercalar heterocytes: the divided trichomes separate one from another, but remain parallely located within the mother sheaths in the colony. Hairs are composed from the narrow, long, hyaline cells. Sheaths firm, sometimes lamellated, colourless or yellow-brown, enveloping all the ˝daughter˝ trichomes, which produce their own','Komárek (1992)',NULL,0,0),(401,298,'description','Non-motile, unicellular rods and oxygenic photoautotroph. Reproduction occurs by transverse binary fission in a single plane. Do not produce well-defined sheath layers. Contain phycoerythrin and photosynthetic thylakoids located peripherally. Require seawater for growth. Contain zeaxanthin, b-carotene and echinenone as major carotenoid pigments.','Choi et al. (2008)',NULL,0,0),(402,295,'description','Trichomes solitary, short, few-20-celled, straight or slightly arcuated, more or less cylindrical along the whole length, without sheaths or gelatinous envelopes, isopolar, slightly constricted at cross-walls. Cells diametric or shorter than wide, blue-green. Heterocytes more or less spherical, develop terminally, on one or (later) on both ends; they are sphe- rical, wider than vegetative cells. Akinetes missing.','komárek (1992)',NULL,0,0),(403,299,'description','Filamentous - colonial; filaments heteropolar, irregularly falsely branched, attached by the bases to the substrate or creeping among detritus and other algae, forming shrub-like colonies, composed from heteropolar trichomes and intensely swollen sheaths. Trichomes solitary or in pairs in one sheath, uniseriate, heteropolar, constricted at cross-walls, with basal heterocytes, in the apical part narrowed in elongated, cellular hair; hair-cells cylindrical, hyaline. Sheaths very thick, swollen, widened, up to 10-times wider than trichomes, firstly closed, later open at the apex, intensely lamellated, at the apex funnel-like divaricated, partly yellowish-brown or brown. Heterocytes basal or intercalar (before the false branching) and secondary at bases of branches, spherical or hemispherical. Akinetes described at trichome bases, more or less spherical, but not well known.','komárek (1992)',NULL,0,0),(404,302,'description','Filamentous - thallous; solitary branched filaments or mats on the substrate. Filaments free or in fascicles, sometimes densely coiled, creeping on the substrate or with erected branches, commonly falsely branched, with one or (obligatory) two lateral branches. Branching initiates after trichome disintegration by help of necridic cells between two heterocytes, usually not at heterocytes; both branches grow parallely aside or in crossing position; the filaments make sometimes typical loop-like lateral formations before branching, in which tops of the trichomes later divide. Trichomes isopolar, cylindrical, not diversified in basal and apical parts,uniseriate, usually with solitary heterocytes, constricted (rarely not constricted) at cross walls; terminal parts of branches cylindrical or slightly widened, with rounded apical cell; middle parts of trichomes sometimes with elongated, cylindrical cells. Sheaths firm, limited, parallel or diverging, lamellated, usually yellow-brown (coloured by scytonemin) in some parts. Cells pale or olive-green, usually with solitary, irregularly disposed granules or with granular content, rarely yellowish or pinkish coloured; apical cells sometimes with large vacuoles. Heterocytes intercalar, solitary, rarely in pairs, cylindrical or barrel-shaped. Akinetes were several times mentioned, but not proved and well described.','Komárek (1992)',NULL,0,0),(405,300,'description','Filamentous - colonial; filaments polarized, thick, containing rarely one, usually several more or less parallely situated trichomes; sheaths fine, slightly or clearly widened, gelatinous, homogeneous, rarely layered or lamellated, with straight or irregularly wavy, limited margin; sometimes fine special sheaths enveloping the simple trichomes occur; sheaths colour1ess or partly coloured, yellow, yellowish-brown, reddish or blue- violet; ends of sheaths characteristically narrowed and bluntly pointed, usually closed, sometimes branched. Filaments in free divaricated, microscopic or up to macroscopic filamentous thallus (subg. Schizothrix), joined in erected fascicles (subg. Symplocastrum Gomont 1892), or incrusted heavily by calcium carbonate and forming more or less hard, hemispherical or layered colonies on the (usually stony) substrate (subg. Inactis (Kutzing) Gomont 1892). Thallus usually joined to the substrate, rarely free (in soil or metaphyton). Trichomes cylindrical, isopolar, not polarized (in contrast to filaments I), usually not attenuated to the ends, unconstricted or slightly constricted at the cross-walls. Cells cylindrical, rarely more or less isodiametrical, usually longer than wide; apical cells mainly conical and rounded, without calyptra and without thickened outer cell wall. Heterocytes and akinetes missing.<br>Cell division crosswise to the trichome axis, without meristematic zone; &nbsp;all cells capable to divide. Reproduction by motile hormogonia, which &nbsp;separate from trichomes probably without help of necridic cells.','Komárek (1992)',NULL,0,0),(406,306,'description','Thallus (colonies) polarized, attached by one end to the substrate, micro- to macroscopic. Initial cells solitary, cylindrical or subspherical to irregularly and narrowly club-shaped, attached by the basal end to the substrate, straight or slightly curved, with colourless and/or later yellowish pseudovagina, later dividing intensely in the upper part and forming pseudofliamentous to irregular, large colonies of aggregated cells; cells are oriented more or less in rows within thallus, or (in old parts) irregularly. Cells sometimes produce their individual mucilaginous, colourless envelopes, which are lamellate in old parts of thallus<br> and yellowish-brown or orange coloured (in one species).','komárek & anagnostidis (1998)',NULL,0,0),(407,306,'description','Colonial; initial cells solitary, cylindrical up to irregularly and narrowly club-shaped, by the basal end attached to the substrate, straight or slightly curved, with colour less and later yellowish pseudovagina, later dividing intensely in the upper part and forming pseudofilamentous up to irregular, rich colonies of cells, which are oriented within thallus more or less in rows or (in old parts) irregularly. Thallus micro-up macroscopic. Cells produce their own mucilaginous colour less envelopes, which are in old parts of thallus lamellated and yellowish-brown or orange coloured.','komárek (1992)',NULL,0,0),(408,301,'description','Thallous; thallus forms mats on the substrate or mixed with other algae, composed from basal, prostrate filaments creeping on the substrate and more or less erected branches; basal trichomes torulous, uni- or multiserial, true or falsely branched, constricted at cross walls, prostrate or semicircularly bent; branches cylindrical, uniseriate, creeping or erected, mainly falsely, repeatedly, tolypotrichoid branched. Sheaths distinct, limited, thick, lamellated, closed or funnel-like open at the apex, sometimes telescopic, usually (in some parts) yellow-brown. Cells barrel-shaped or almost cylindrical, pale or olive-green, slightly or regularly granular, sometimes with distinct solitary granules. Heterocytes develop intercalarly, solitary or in pairs, usually unipored (before false branching), cylindrical, hemispherical or almost spherical. Akinetes not found.','komárek (1992)',NULL,0,0),(409,307,'description','Colonies microscopic, free floating, more or less spherical, composed of radially and slightly irregularly divaricate thick, tube-like, colourless stalks, originating from the colonial center. Cells narrower than stalks, situated within the end of stalks; the whole stalk system with cells is enveloped by the common, fine, diffluent, colourless mucilage; stalks slightly distant from one another. Cells in strings solitary or grouped in twos after division, geminate.','komárek & anagnostidis (1998)',NULL,0,0),(410,307,'description','Unicellular - colonial; colonies microscopic, +/- spherical, subspherical up to irregularly oval, mucilaginous, multicelled, free living (planktic), enveloped by fine, unstructured, colourless, indistinct, gelatinous envelopes; cells situated solitary or in twos (after division) within the end parts of fine, mucilaginous, colourless, tube-like sheaths opened at the ends, radially oriented and pseudodichotomously branched, originating from the centre of a colony; between single tube-like sheaths are spaces. Cells spherical, after division hemispherical, pale yellowish, blue-green, without aerotopes, in the colony placed +/- peripherally.','komárek (1992)',NULL,0,1),(411,308,'description','Filamentous; filaments joined in gelatinous mats and later more or less erected fascicles, usually long, commonly branched (only sheaths), with limited, more or less cylindrical, firm, homogeneous, widened, colourless or slightly yellowish sheath, which is in small distances transversally constricted, but not longitudinally lamellated. Sheaths contain several up to greater number of trichomes sometimes freely, later densely parallely aggregated in fascicles. Trichomes cylindrical with straight ends, usually unconstricted at cross walls. Cells more or less isodiametrical or slightly longer or shorter than wide, without calyptra.','komárek (1992)',NULL,0,0),(412,303,'description','Filamentous - thallous; solitary branched filaments, clusters with parallely or irregularly arranged filaments or mats on the substrate. Filaments free or densely coiled, creeping on the substrate, or joined to the substrate by middle parts and free ends of branches, sparsely or commonly falsely branched, usually with two (rarely with one) branches. Branching initiates after trichome disintegration by help of necridic cells, rarely after loop-formation, not at heterocytes. Trichomes isopolar, but sometimes (young trichomes) forming Homoeothrix-like heteropolar stages; ends of young trichomes and branches cylindrical with rounded terminal cells, but later always distinctly narrowed and sometimes with elongated, cylindrical, vacuolized apical and subapical cells; trichomes constricted or unconstricted at cross walls. Sheaths firm, limited, hyaline or (usually) parallely lamellated and telescopic, in majority of species yellowish-brown in old specimens. Cells shorter or longer than wide, variable in length, pale or olive-green, rarely pinkish or bright blue-green, towards the ends elongated and vacuolized, always without gas vesicles; numerous necridic cells. Heterocytes develop in dependence on the nitrogen concentration, intercalar, usually solitary, cylindrical or barrel-shaped, of diffe- rent length. Akinetes described only rarely in rows (revision necessary).','komárek (1992)',NULL,0,0),(413,304,'description','Filamentous-thallous; filaments composed from trichomes and sheaths; trichomes of two types, torulous,creeping on the substrate and cylindrical, erect, joined parallely in densely agglomerated fascicles (macroscopically visible); creeping filaments uni- or (rarely) multiseriate, hypothallic, sometimes true branched (T-type of branches), with more or less barrel-shaped cells and solitary intercalar, barrel-shaped heterocytes; erect trichomes more or less cylindrical, constricted or unconstricted at cross walls, with solitary intercalar, usually cylindrical (sometimes very long) heterocytes. In both basal and particularly erect filaments common false branching, usually with one lateral branch (rarely with two branches),diverging at heterocytes. Sheaths thin, firm, usually not la- mellated, colourless. Cells pale, olive or bright blue-green, with solitary distinct granules. Akinetes not known.','komárek (1992)',NULL,0,0),(414,312,'description','Filamentous - thallous; filaments free, creeping or erect, sometimes in fascicles, irregularly branched. Trichomes in basal parts mostly torulous, with distinct constrictions at cross walls, uniseriate or (rarely) biseriate, with rare true branching (T-type); young trichomes and branches cylindrical; irregular false branching commonly occurs in younger trichomes, developing by help of necridic cells, with one, rarely two branches; branches waved, cylindrical or with waved sides; terminal parts of trichomes cylindrical or slightly widened, end cells widely rounded. Sheaths firm, thin or thick, usually slightly lamellated. Cells blue-green, isodiametric or slightly longer or shorter than wide, usually with solitary distinct granules in the cell content. Heterocytes rare, intercalar, solitary, sometimes lacking. Akinetes were described in one species, in rows in old trichomes.','komárek (1992)',NULL,0,0),(415,309,'description','Snowella comprises free-living, spherical or oval microscopic colonies, sometimes composed of subcolonies, that have a central system of thin, nearly pseudodichotomously divided gelatinous stalks (may be confluent) that bear cells at their ends (periphery of colony). Colonies are enveloped by very fine, unstructured, and diffuse mucilage. Cells are spherical or slightly radially elongated, and pale blue-green, olive green, or<br> yellowish in color; one species may be pinkish. Two species have one or a few central aero-topes. The cells are 0.6-4.2 μm in diameter (or long). Cell division is by binary fission in two planes, perpendicular to one another and to the colonial surface. Reproduction is by disintegration of colonies.','Komárek (2003)',NULL,0,0),(416,309,'description','Colonies more or less spherical or irregularly oval, rarely compound, free floating, with distinct or indistinct (staining !), homogeneous, colourless and wide mucilaginous envelopes. Within colonies there is a more or less stable system of fine, thin, thread-like mucilaginous stalks radiating from the colonial center, more or less pseudodichotomously divaricated and sometimes fasciculate, widened in the center. Cells spherical or slightly elongate, joined to the ends of stalks during the whole life cycle, distant from one another. If the cells are densely disposed on the periphery of old multicellular colonies, there always remain at least narrow spaces between them; cells usually not strictly in one peripheral layer, but slightly radially shifted from one another.','Komárek & Anagnostidis (1998)',NULL,0,0),(417,309,'description','Unicellular - colonial; colonies microscopic, +/- spherical or irregularly oval, rarely composed, free living (floating), with indistinct, smooth, colourless, fine and wide mucilaginous envelopes;<br> within the colonies a system of fine, thin (thread-like), +/- stable, mucilaginous, +/- pseudodichotomously branched and sometimes fasciculating stalks, which are sometimes widened in the centre. Cells spherical or slightly radially elongated, joined to the ends of stalks during almost the whole life cycle, distant from one another, sometimes slightly radially shifted to one another (if the cells are densely disposed in old colonies, always remain at least narrow spaces between them); cells pale greyish blue-green, yellowish or pinkish, without or with solitary central aerotopes (granules ?).','Komárek (1992)',NULL,0,1),(418,305,'description','Filamentous; filaments (trichomes) solitary, free living, immotile, without gelatinous sheaths or envelopes, torulous, simple, not branched, composed from spherical cells and at one end narrowed, with ellipsoid-cylindrical, slightly elongated cells. Cells pale blue-green, with solitary large, prominent granules within the cell content. Heterocytes and akinetes not known.','komárek (1992)',NULL,0,0),(419,313,'description','Colonies microscopic, free-floating, in young stages small hollow spheres or irregular, later hollow, spherical, broadly elliptical, cylindrical or irregular in shape, with holes in the colony surface, slightly flattened, sometimes clathrate; mucilaginous envelope narrow, diffluent, inconspicuous, colourless; cells spherical, initially loosely arranged, later more or less densely arranged, always on the colony surface; cell content with aerotopes.','Azevedo et Sant\'Anna (2003)',NULL,0,0),(420,311,'description','Thallus composed of epilithic (mainly petrified), and endolithic, coiled and/or, curred pseudofliaments with apical and/or intercalary growth. Epilithic part (if developed) spreads over the surface of limestone substrates and is composed of simple, short uniseriate or multiseriate rows of spherical or slightly elongate, irregularly disposed cells, intensely calcified; endolithic pseudofliaments are common, long, enclosed within widened mucilaginous stalks, within which is a uniseriate row of solitary, usually elongate cells, which are distinctly distant one from another; at the ends of pseudofliaments one enlarged, oval, obovoid, club- shaped or irregular terminal cell is developed; cells within pseudofliaments are distant from one another, separated by a transversely layered mucilage. All pseudofliaments are enveloped by wide, lamellate, gelatinous sheath, sometimes icoloured, pseudodichotomously or laterally and repeatedly divaricate («branched»), sometimes widened at the apex (the cells are sometimes wider in the apical parts of branches than near their bases); lateral branches develop after the lengthwise division of apical cells (or cells in their apical parts) in endolithic pseudofilaments and grow perpendicularly or obliquely to the stony surface. Cells are of irregular shape, more or less spherical or elongate, with more or less homogeneous, pale blue-green content.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(421,311,'description','Unicellular - colonial; thallus composed from epilithic and endolithic pseudofilaments. Epilithic part spread over the surface of limestone substrate, composed from simple and short uniseriate or multiseriate rows of spherical or slightly elongated, irregularly disposed cells; endolithic pseudofilaments are common,long, mucilaginous stalks, at the ends of which is situated one enlarged, oval, obovoid, club-shaped<br> or irregular end cell, rarely uniseriate with a row of solitary cells, distant one from another, separated by a crosswise layered mucilage; all pseudofilaments are enveloped by wide, lamellated, gelatinous sheath, sometimes coloured, pseudodichotomously or laterally divaricated (˝branched˝); lateral branches develop after the division of apical cells in endolithic pseudofilaments. Cells of irregular shape, more or less spherical up to elongated, with more<br> or less homogeneous, pale blue-green content.','komárek (1992)',NULL,0,1),(422,311,'description','Lager epilithisch, weit ausgebreitet, von unbestimmter Gestalt, aus aufrechten, freien, niemals erwachsenen „Fäden˝ bestehend, welche gegen die Basis zu verjüngt und aus einer Reihe von Zellen gebildet sind; zwischen den Zellen große Stücke von Membranhüllen, welche einseitig von den Zellen gebildet werden: Membranhüllen dick, geschichtet. „Verzweigungen˝ entstehen dadurch, daß interkalare Zellen, anscheinend infolge von Druck der umgebenden Membranteile, seitlich herausgepreßt werden und<br> von neuem zu wachsen beginnen. Fortpflanzung durch Freiwerden einzelner apikaler Protoplasten und Austreten aus der Membranhülle (Gonidien).','Geitler (1932; sub<i> Hormathonema</i>)',NULL,0,0),(423,310,'description','Filamentous, heteropolar; filaments uniserial, not branched, solitary or in groups, attached to the substrate (= legs of Hydracarines) by a small, cup-shaped sheath, narrowed on the basis into a short leg (pad); trichomes with slightly widened, rounded basis, without a heterocyte, enveloped by the short sheath, cylindrical, slightly and gradually narrowed to the ends, constricted at the cross-walls. Cells shorter than wide, to the ends up to isodiametrical or slightly longer than wide, end cells narrowed, more or less conical and rounded, never elongated into hairs.<br>','komárek (1992)',NULL,0,0),(424,315,'description','Colony softly mounded on agar, with slightly irregular margins, not tufted, dark blue-green, maintaining its colour at four months; the only evidence of colour change to olive or ochre occurring with cell death in drying, older cultures. Colony compact, with densely arranged filaments, but no evidence of external mucilage production. Although filaments can be seen within the colony at 30x magnification, filaments do not extend horizontally or vertically from the colony. Colony morphology is similar on both Bold´s Basal and Z-8 media. Filaments forming tight, regular spirals which can be seen to taper slightly in young cultures. Filaments 6-20 um in diameter; spirals 16-28 urn in diameter at their widest point, tapered end of spirals about 75-80% of the maximum diameter; distance between regular spirals 8-12(-16) um. Some filaments more loosely coiled, or even extended; these filaments increasing in frequency in older cultures. Both single and double false branching occasionally observed in more loosely coiled or extended filaments, but not in tightly spiraled filaments. False branching usually distant from the heterocytes. Sheath firm, usually colourless, occasionally golden to brown, thin in young cultures becoming thicker and lamellated in older cultures, 1-4 um thick. Trichomes not to slightly constricted at the crosswalls, more commonly constricted in older cultures and in loosely coiled or extended filaments, 5.5-14.0 um in diameter.Cells mostly shorter than wide, occasionally quadratic, 2.0-7.2 um long, without aerotopes, cell contents sometimes granular, especially in older cultures. Heterocytes both intercalary and basal within filaments, mostly single but occasionally double in intercalary position, rarely triple, spherical to oval, sometimes appressed on one side in basal position, light brown, 8-9 um in diameter, 4-9 um long.<br> Differs from Scytonema and Tolypothrix in that the filaments are regularly, tightly coiled in a right-handed helix. Filaments free, forming tight, regular spirals. False branches double or single. Sheaths firm, thin to thick, sometimes lamellated. Trichomes solitary within the sheath. Cells shorter than broad. Heterocytes both intercalary and basal, spherical to oval or appressed. Akinetes not observed.','flechtner et al.(2002)',NULL,0,0),(425,319,'description','Filamentous - thallous; thallus gelatinous, firm, flat, crusty, composed from basal, creeping, coiled filaments, from which grow numerous erect, densely parallely oriented, not very long branches, which are repeatedly divaricated. Trichomes in creeping filaments multiserial, sometimes disintegrating, in chroococcoid mass, from which grow erect trichomes - branches (T-type of branching); erect trichomes uniseriate, repeatedly V-like true branched, branches grow more or less parallely and perpendicularly to the substrate. Sheaths thin, firm, colourless, sometimes slightly gelatinizing at sides, not or slightly lamellated, closed at the apex of young trichomes; trichomes mainly torulous, with clear constrictions at cross walls, more or less cylindrical or slightly widened to the ends, with broadly rounded terminal cells. Cells irregular rounded or barrel-shaped, isodiametric or slightly longer or shorter than wide. Heterocytes intercalar, rounded barrel- shaped. Akinetes not known.','komárek (1992)',NULL,0,0),(426,318,'description','Filamentous; filaments unbranched, uniserial, isopolar, solitary, short or variable in length, straight to helically twisted, more or less equally wide along the whole length, about 15 um wide and slightly torulose, without sheaths or with delicate sheaths 3 um thick following the contours of the cell; trichomes flattened and triradiate in transverse section slightly constricted at the cross walls, immotile. Cells shorter than broad, in cross section with broad arm-like projections 120 degrees apart, separated by U-shaped depressions, arms broaden somewhat toward their extremities which may be obtuse to truncate at outer edge; pigmentation is concentrated in arms. Thylakoids localized along the cell walls and more agglomerated and coiled within the protrusions. Cell content blue-green, without prominent granules and inclusions. Heterocytes and akinetes are missing.','komárek (1992)',NULL,0,0),(427,316,'description','Filamentous; filaments unbranched, always without sheaths, rarely solitary (free floating), usually in clusters or in fine mats which are up to macroscopicall visible and covering the substrate regularly screw- like coiled along the whole trichome length, with unchanged width of screws (very rarely is the spirality destroyed as anomalies); screws are very densely tight, touching one to another or with small spaces between them, trichomes:spirals width ratio being (2)-2.5-(4). Trichomes isopolar, 0.5-3(6?) um wide uniserial, compoused of cylindrical cells, unconstricted at the cross walls which are usually unvisible in light microscope, not attenuated towards the ends, intensely motile (rotation). Cells without aerotopes and prominent granules, more or less isodiametric, less (?) or longer than wide, usually with homogeneous content, pale blue-green, olive green or pinkish, with changeable PC: PE ratio, with asymmetrically localized thylakoids near the “outer” walls, with special perforation of the side walls (cf. Guglielmi et Cohen-Bazire 1982; all species ?); end cells widely rounded, without thickened cell walls or calyptras. Heterocytes and akinetes absent.','Komárek (1992)',NULL,0,0),(428,317,'description','Cells solitary or in groups, more or less spherical, usually attached to the substrate by any side (cells are not polarized), secondarily (and in cultures) in free or attached irregular, usually microscopic aggregates. Cells in a colony of variable size, with homogeneous, pale blue-grey, blue-green, yellowish, olive-green, reddish to dark red or violet content. Sheaths (vaginae) thin, firm, mucilaginous, colourless, forming a narrow hyaline layer («wall») around solitary cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(429,317,'description','Solitary cells (up to 40 um in diam.) or irregular groups of cells,  joined to the substrate and one to another. Cells spherical or slightly widely  oval, attached to the substrate by any part of a cell wall. Around the cells  firm, thin, colourless sheaths, opened in any place of the surface during  reproduction. Cell content greyish blue-green or reddish, thylakoids in parallel  fascicles in the peripheral layer or irregularly through the whole cell volume;  always without aerotopes.','komárek (1992)',NULL,0,1),(430,320,'description','Cells solitary or in groups, more or less short cylindrical or club-shaped; heteropolar, elongate, attached by one end to the substrate usually by a mucilaginous pad, very soon (during the cell development) dividing transversely and successively into uniseriate, cylindrical, straight or curved, pseudofilamentous rows of numerous exocytes (sometimes very long), enveloped by firm, colourless sheath (pseudovagina), which later opens at the apex; exocytes remain for long time in pseudofilamentous formations. Cell content pale blue-geen, greyish blue, olive-green, sometimes with visible keritomy (position of thylakoids  in fascicles throughout the whole cell) and solitary granules.','Komárek & anagnostidis (1998)',NULL,0,0),(431,320,'description','Unicellular; cells elongated, always polarized, attached to the  substrate by their basal ends by help of a morphologically diversified pad,  which is the basal part of the firm, thin, usually layered sheath (pseudovagina),  solitary or in groups; young cells oval, cylindrical or obovate, which start  usually very soon divide into a row of exocytes forming the long pseudofilaments  within the mother sheaths (adult individuals); pseudovaginas are open at the apical ends. Cell content pale blue-green, cells sometimes with several prominent granules, thylakoids more or less coiled, distributed all over the cell (generic character ?).','komárek (1992)',NULL,0,0),(432,322,'description','Filamentous – thallous; thallus pulvinate, woolly, up to 1.5 cm thick, greyish blue with many densely coiled or more or less parallely arranged filaments, some- times joined in erected fascicles. Filaments irregularly branched, not distinctly morphologically diversified in basal sections and branches. Trichomes uniseriate, probably isopolar, with cells rarely shorter or (usually) longer than wide, cylindrical, not constricted or slightly constricted at cross walls, not attenuated towards the ends, with rounded terminal cells. Branching of two types, true or reverse V-type, and false, scytonematoid; branching initiates always distant from heterocytes (reverse V-branching originates always from special oblong cells, located between two shortened cells, containing densely granular and deeply coloured content; later the oblong cell lengthwise divides and new cells elongate). Sheaths firm, limited, homogeneous or slightly lamellated, brownish in old parts. Cells blue-green, with slightly granular content. Heterocytes intercalar, more or less cylindrical, solitary. Akinetes not observed.','Komárek (1992)',NULL,0,0),(433,323,'description','Filamentous - thallous; thallus wooly, in cushion-like patches,  blue-green or brownish, with irregularly, densely coiled, branched filaments.  Filaments slightly diversified in thicker main filaments and thinner branches, not polarized. Trichomes in main filaments cylindrical, constricted at cross  walls, usually with cells shorter than wide, rarely isodiametrical or longer  than wide, with numerous true branchings of reverse V-type, occasionally with false branching, which starts usually after disintegration of trichomes at heterocytes; trichomes in branches more or less cylindrical, with cells shorter (during intense division) or longer than wide, without constrictions at cross walls or with constrictions (regularly in segments from which hormocysts develop). Cells blue-green, with solitary prominent granules. Sheaths distinct, firm, hyaline, not lamellated, in hormocysts thick, dark brown, but also not lamellated. Heterocytes terminal ( in germinating hormocysts and after trichome disintegration) and intercalar, more or less spherical or shortly cylindrical, in branches cylindrical. Akinetes not found.','komárek (1992)',NULL,0,0),(434,321,'description','Filamentous - thallous; thallus wooly or crusty, composed from free, coiled, true branched filaments, usually attached to the substrate, not diversified distinctly in basal filaments and branches. Trichomes two or multiseriate (only in young trichomes and at ends of branches uniseriate), sometimes very thick, irregularly laterally true branched (T- and V-type of branching), irregularly coiled, sometimes narrowed (with less number of cell rows) towards the ends, apical cell is sometimes larger than the other ones. Sheaths thin or thick, limited, later wide, lamellated and usually yellowish-brown; around cells in old parts of filaments sometimes special envelopes (trichomes disintegrating in separated cells within filaments). Cells barrel-shaped or roundly irregular, connected usually by one pore (˝pit connections˝) one with another, which disappear in some segments of trichomes; cell content blue-green or olive green, usually with prominent solitary granules. Heterocytes intercalar, solitary, rarely lateral, in a similar form as neighbournig vegetative cells. Akinetes not known. Sometimes chroococcoid cell clusters arise.','komárek (1992)',NULL,0,0),(435,324,'description','Filamentous - colonial; colonies in form of flat mats on the substrates (initial stages), from which grow up vertically erected fascicles of filaments, specifically coiled and parallely oriented; erected fascicles form occasionally small, characteristical ˝grass-like˝ mats. Fascicles (not filaments) are sometimes branched or anastomotic. Trichomes solitary, slightly coiled, cylindrical, usually not constricted at cross walls, enveloped obligatory by firm, thin, sometimes outside gelatinized sheaths. Ends of trichomes usually cylindrical, rarely slightly attenuated. Cells cylindrical, without aerotopes and usually without prominent granules, terminal cells rounded, without calyptras.','Komárek (1992)',NULL,0,0),(436,326,'description','Cells solitary or grouped in microscopic or macroscopic, irregular clusters, but not forming mucilaginous colonies; cells sometimes in short series of pseudofilamentous formations with 2-4 (20) cells. Mucilage absent or very fine, colourless, homogeneous, diffluent, around single cells. Cells long oval or cylindrical, sometimes several times longer than wide, straight, arcuate or sigmoid, 1.5 up to more than 20 um long and 0.4-6 (11) um wide, with parietal thylakoids; fine subunit arrays with p4 symmetry were found in few Synechococcus strains. Particularly in cultures there can arise long filamentous involution forms.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(437,326,'description','Unicellular; cells live solitary or agglomerated in groups, but without common mucilage, oval, widely oval or rod-like, sometimes curved or sigmoid, rounded at the ends, with homogeneous content or with several dispersed or solitary polar granules, usually pale blue-green, rarely olive green, bright blue-green or pinkish, immotile. Without chromatic adaptation. Thylakoids localized along cells walls. Filament-like involution cells. Photoautotroph.','komárek (1992)',NULL,0,1),(438,326,'description','Zellen ellipsoidisch bis zylindrisch, gerade, selten leicht gebogen, an den Enden abgerundet, einzeln oder zu zweien, nur ausnahmsweise zu vieren aneinanderhängend, ohne oder mit kaum sichtbarer, dünner Gallerthülle. Teilung quer. Zellen manchmal aktiv beweglich  (Planokokken - Stadium).','Geitler (1942)',NULL,0,1),(439,326,'description','Zellen ellipsoidisch bis zylindrisch, gerade, an den Enden abgerundet, einzeln oder zu zweien, nur ausnahmsweise zu vieren aneinanderhängend, ohne oder mit kaum sichtbarer sehr dünner Gallerthülle. Teilung quer. Zellen manchmal beweglich (Planococcen-Stadium).','Geitler (1932)',NULL,0,1),(440,327,'description','Cells solitary, spherical, after division hemispherical and for a short time two together, never forming colonies, without mucilage or (mainly) with narrow, fine, colourless and usually diffluent and indistinct mucilaginous envelopes. Cells spherical or widely oval. In several strains the cell walls contain a special  «S-layer» with characteristical hexagonal (p6) substructure (Šmarda et al. 1979; Vaara 1982; etc.) (fig. 154). The stability, function and taxonomic significance of this layer is not yet clear. Different but stable pigment ratios in related species (and populations) have been found (Kováčik in litt.).','komárek & anagnostidis (1998)',NULL,0,0),(441,327,'description','Unicellular; cells live solitary or agglomerated, but without common mucilage, spherical or slightly widely oval before division, sometimes enveloped by own thin, fine, colourless, diffluent mucilaginous envelope (staining !), with homogeneous content or with several prominent granules, sometimes with visible chromatoplasma, pale blue-green, olive-green, bright- green or pinkish.','Komárek (1992)',NULL,0,0),(442,327,'description','Zellen kugelig, einzeln, nur nach der Teilung zu zweien und dann ungefähr halbkugelig,ohne sichtbare Gallerthülle oder bei den großzelligen Arten mit dünner Hülle.','Geitler (1942)',NULL,0,0),(443,327,'description','Zellen kugelig, einzeln, nur nach der Teilung zu zweien beisammen, ohne sichtbare Gallerthülle (atypisch: S. crassa).','Geitler (1932)',NULL,0,0),(444,329,'description','Filamentous – thallous; thallus in form of mats on the substrate  with more or less parallely oriented or slightly-coiled creeping filaments-with  not very common true branches. Trichomes uniseriate, not distinctly diversified,  old  more torulous, young ones cylindrical and sometimes slightly thinner,  both constricted at cross walls, not attenuated toward the ends, with rounded  terminal cells. True branching of T-type, lateral; branches bent soon into  the direction of the original trichome.<br>   Sheaths thick, lamellated, gelatinizing  from outside and confluent sometimes with neighbouring sheaths. Cell barrel-shaped  or cylindrical, with finely granular content. Heterocytes intercalar, barrel-shaped, solitary, not very common. Akinetes described, small, developing serially in rows in old trichomes, with thickened cell wall.','komárek (1992)',NULL,0,0),(445,336,'description','Lager endolithisch, von unbestimmter Gestalt, unterhalb der Oberfläche in Steinen ausgebreitet, aus senkrecht zur Oberfläche des Substrats orientierten Fäden bestehend. Fäden frei, durch Querteilung wachsend, mehr oder weniger parallel zueinander, einreihig; Verzweigung seitlich, durch eine Ausstülpung des oberen Teiles der Zellen eingeleitet, niemals dichotom. Zellen viel länger als breit, zylindrisch. Endosporen unbekannt.','Geitler (1932)',NULL,0,0),(446,331,'description','Filamentous - colonial; thallus in form of flat gelatinous mats  with densely interwoven filaments attached to the substrate. Trichomes heteropolar,  uniseriate, with basal and intercalar heterocytes, more or less cylindrical,  slightly tapering to the ends, constricted at cross walls. Sheaths thin, narrow, limited, fine, colourless, unlayered. Cells more or less cylindrical, rectangular with slightly rounded ends, with very pale blue-green or almost colour less content, not divided in chromato- and centroplasmic regions, sometimes with solitary, prominent granules (probably sulphur granules); the end cells conical-rounded. Heterocytes hyaline/spherical or elipsoidal in terminal (basal) positions, cylindrical (rectangular) when intercalar; basal heterocytes develop from end cells, or intercalarly from two neighbouring divided cells, from which arise two heterocytes one near another; the trichome divides between two intercalar heterocytes, which remain later in terminal position. Akinetes were not observed.','komárek (1992)',NULL,0,0),(447,335,'description','Solitary filaments or (mainly) periphytic mats, clusters and strata, which are composed from +/- coiled trichomes enveloped by colourless, fine or limited mucilage, without prominent sheaths; strata sometimes macroscopic.  Tri- chomes uniseriate, isopolar, metameric, irregularly coiled, in later  stages with several solitary, intercalar heterocytes which are usually situated  in +/-regular distances in the trichome one from another, mainly clearly constricted at the cross walls, to the ends not attenuated, without any branching; end cells rounded or conical. Cells spherical, barrel-shaped or cylindrical, always without aerotopes. Heterocytes spherical, oval or cylindrical. Akinetes develop always apoheterocytic, i.e., they start to develop from vegetative cells in the middle between two heterocytes and later change all or almost all vegetative cells into akinetes, towards heterocytes.','komárek (1992)',NULL,0,0),(448,338,'description','Filamentous; filaments solitary, free floating or coiled in clusters  or fine strata, planktic, tychoplanktic, benthic or metaphytic, straight,  arcuated or freely irregularly coiled, many-celled, up to 5 mm long, isopolar,  without sheaths or facultatively with very fine and indistinct mucilaginous  enveloping layers. Trichomes cylindrical, isopolar, not attenuated to the  ends, unconstricted (or indistinctly constricted) at the cross walls, more  or less isodiametric or slightly longer or shorter than wide, with thin cell  walls, 2-16 um wide, without any branching, without or with reduced motility;  end cell 5 rounded, usually with thickened  outer cell wall or with narrow  calyptra. Cells mostly cylindrical, pale blue-green, yellowish or reddish,  always without gas vesicles, but sometimes intensely vacuolated during prominent  phases of vegetation cycles and with keritomized chromatoplasma (special  location of thylakoids combined with vacuolization). Changeable phycobilin  pigments ratio, usually with higher content of phycoerythrin. Heterocytes  and akinetes absent.','komárek (1992)',NULL,0,0),(449,339,'description','Filamentous; filaments solitary, free floating, in young stages  isopolar, later branched, without diversified basal parts, straight or slightly  curved. Young trichomes uniseriate, isopolar, not branched, more or less constricted at cross walls, continually attenuated to the ends, with terminal cells elongated, narrow, rounded (Raphidiopsis-like stage); later stages with developing intercalar solitary heterocytes and oval akinetes, sometimes with true branching (T-type); branches initiate by the longitudinal division of the parental cell. Sheaths fine, gelatinous,wide, hyaline, diffluent (staining !). Cells cylindricalor irregular barrel-shaped, usually longer than wide, only after intense division shorter than wide, cell content pale blue-green with gas vesicles (visible aerotopes). Heterocytes occur usually scarcely (common only in nitrogen deficient environment), spherical or oval, akinetes solitary or in short irregular rows, oval, thick-walled, widely oval up to almost spherical.','komárek (1992)',NULL,0,0),(450,337,'description','Colonies in the form of an amorphous, gelatinous mass, spreading over the substrate, composed of more or less cylindrical tubes, densely and more or less parallely arranged, sometimes wider in some sections than others, unbranched; sheaths fine and scarcely visible or with distinct margin, rounded or truncate at the ends, later open. Within the sheaths a uniseriate row (rarely 2-3 rows) of usually “zig-zag” disposed cells, rarely in straight, wavy or screw-shaped formations. Cells elongate, oval to cylindrical, enveloped by very fine, colourless, scarcely visible gelatinous envelopes (staining !), slightly distant from or touching one another.','komárek & anagnostidis (1998)',NULL,0,0),(451,337,'description','Unicellular - pseudofilamentous - colonial; colonies widely spread  in a thin layer on the substrate,_gelatinous, blue-green, composed from densely,  more or less parallel oriented sheath-like tubes, in which are the cells  in one row or (later) in zig-zag or slightly screw-like coiled rows, rarely  organized irregularly. Sheaths simple, sometimes slightly widened, colourless,  sharply limited or diffluent, not layered, at the ends roundly closed, or  (after escaping, of solitary cells) opened and cut, (3.3)4 - 6.7 (8.3) um  wide. Cells elongated, ellipsoid, oval or cylindrical with rounded ends, with solitary large granules within plasma, touching one to another by their ends.','komárek (1992)',NULL,0,1),(452,344,'description','Filamentous - colonial; colonies macroscopic, gelatinous, smooth on the surface, more or less cylindrical or subspherical, sometimes tube-like, submersely living. Trichomes of the same width along the whole length, more or less straight or slightly curved, uniseriate, not branched, not attenuated or widened at the ends, intensely constricted at cross walls; terminal cells rounded; irregularly or more or less parallely and densely arranged in common, diffluent mucilage. On the surface of colonies is the fine pelicula; sheaths around trichomes are absent. Heterocytes intercalar, solitary, causing probably the metameric structure of trichomes. Akinetes arise paraheterocytic, at both sides of heteocytes, in short series, spherical or oval.','komárek (1992)',NULL,0,0),(453,345,'description','Solitary pseudofilaments, simple, unbranched, to 12 um wide, composed from thin or wide sheaths and (inside) from 1-4 straight, uniseriate rows of cylindrical cells; cells situated one after another, close to or distant from one another (if more rows are within sheaths, they are arranged parallel to one another). Sheaths smooth, structureless and homogeneous, colourless, or thin, firm on the marginal surface. Cells rod-shaped, long cylindrical, more or less rounded at the ends, usually several times longer than wide. <br>','komárek & anagnostidis (1998)',NULL,0,0),(454,345,'description','Unicellular - pseudofilamentous; pseudofilaments solitary, not  branched, containing 1-4 more or less parallel rows of elongated, cylindrical  cells, enveloped by colourless. wide and not stratified, homogeneous envelope  different width; cells are situated in pseudofilaments; serially one after  another, not touching and slightly distant one from another. Cells cylindrical  or rod-like, with solitary prominent granules (always ?) at their apexes,  pale blue-green.','komárek (1992)',NULL,0,0),(455,341,'description','Filamentous- thalous; thallus composed from free, irregularly  coiled, creeping, intensely laterally true branched filaments. Trichomes always uniseriate, morphologically not diversified in ˝main˝ filaments and branches, .cylindrical, not constricted at cross walls, of the same width, only little attenuated to the ends of branches; terminal cells rounded; true branching of the T-type. Sheaths thin, firm, homogeneous, not lamellated, colourless (only walls of hormocysts are yellowish-brown). Cells blue-green, with solitary granules, usually longer than wide. Heterocytes intercalar, solitary, cylindrical. Akinetes not well known and described.','komárek (1992)',NULL,0,0),(456,340,'description','Filamentous - thallous; thallus more or less spherical, gelatinous,  firm, yellow- brown, macroscopic (up to 1 mm in diameter), with continual  smooth surface, inside in mucilage with irregularly arranged (in the peripheral  parts more or less radial) coiled filaments. Trichomes irregularly waved,  uniseriate, constricted at cross walls, of the same width along the whole  length, not attenuated, with wide rounded terminal cells, sometimes true branched (T-type ?). Sheaths around trichomes visible at the periphery of a colony, wide,homogeneous or finely lamellated, yellowish-brown, in the middle of colony diffluent, colourless, homogeneous. Cells barrel-shaped, more or less isodiametrical or slightly longer than wide, blue-green. Heterocytes common, solitary, intercalar or terminal, spherical or slightly elongated. Akinetes not known.','komárek (1992)',NULL,0,0),(457,347,'description','Cells attached to the substrate, solitary or in monolayered groups, sometimes forming blastoparenchymatous colonies or a crustose or flat thin thallus with densely arranged cells; young stages characterized usually by discontinuous groups of sessile cells, sometimes with spaces between one another. Cells more or less polarized, sometimes slightly or distinctly elongate along the vertical axis (this polarity is particularly recognizable ill solitary cells). Around cells usually firm, less frequently gelatinous sheaths. Cells in old colonies are sometimes organized into short, horizontal, irregular rows. All cells more or less the same size, at the colonial margin usually rounded or elongate.','Komárek & anagnostidis (1998)',NULL,0,0),(458,347,'description','Unicellular - colonial; cells attached to the substrate in one  layer, forming flat up to pseudoparenchymatic, circular or elongated in outline  colonies; colonies microscopic, later composed from densely agglomerated cells. Cells more or less spherical, subspherical, oval, irregular, polygonal with rounded corners, or slightly pyriform, usually enveloped by colour- less, thin, firm or diffluent, sometimes slightly layered, tight or slightly widened mucilaginous sheaths; cell content blue-green, greyish or reddish.','komárek (1992)',NULL,0,1),(459,347,'description','Thallus entweder dauernd eine festgewachsene, einschichtige blastoparenchvmatische Scheibe, oder nur in der Jugend scheibenförmig und später durch Bildung aufrechter Fäden mehr oder weniger halbkugelig oder flach krustenförmig, oder aus locker vereinigten Zellen bestehend, dann aber mit meist deutlicher Polarität der Zellen. Aufrechte Fäden, wenn vorhanden, kurz und wenigzellig, anfangs unverzweigt, frühzeitig an den Spitzen dicho- bis tetrachotom verzweigt, seitlich miteinander verwachsen und zu einem scheinbaren parenehymatischen Lager zusammenschließend. Zellen durch schnell aufeinanderfolgende Teilungen oft in Vierer- oder Achtergruppen. Sporangien, wenn vorhanden, in den Scheiben randstendig, in den aufrechten Fäden terminal. Endosporen zu vielen sukzedan gebildet; entleerung der Endosporen durch Aufreissen oder durch verschleimung der Wand.','Geitler (1932)',NULL,0,1),(460,343,'description','Filaments solitary or in clusters, cylindrical along the whole length, ± straight or slightly coiled, with facultative sheath, sometimes in dense, irregular fascicles with colorless and diffluent slime, not enveloped together by a firm, wide sheath. Sheaths around single trichomes thin, ± fine but firm, colorless, sometimes diffluent, attached to trichomes. Never falsely branched. Trichomes cylindrical, not or only very slightly (exceptionally) constricted at cross walls, not attenuated or widened towards ends, without calyptra. Cells isodiametric, rarely shortened to ½ of their width, or up to 2× longer than wide, sometimes with different length in one and the same trichome, cylindrical, pale blue-green, usually with scattered larger granules, which are sometimes gathered more at cross-walls; apical cells cylindrical, rounded at the apex, without calyptra. Position of thylakoids in cells mostly parietal with few occasional irregularities (dependent on environmental conditions). ','strunecký et al. (2011)',NULL,0,0),(461,346,'description','Colonies more or less spherical or irregular oval, commonly composed of subcolonies, free-living, usually with a narrow, colourless enveloping mucilaginous layer.  In the center of colonies is a system of radially and more or less parallely oriented, simple, unbranched stalks, which split along their whole length after cell division; stalks thick, usually as wide as the width of cells, commonly densely packed together and so causing the radial lamellation of the central colonial mucilage (staining !); the stalk system sometimes diffluent within old colonies. Cells rarely almost spherical, usually slightly elongate, widely oval, oval or obovoid, separating from one another immediately after division, but in old colonies very densely, radially aggregated in the peripheral layer. <br>','komárek & anagnostidis (1998)',NULL,0,0),(462,346,'description','Unicellular - colonial; colonies microscopic, +/- spherical or  irregularly oval, usually composed from subcolonies, free living (plankton,  metaphyton), with +/- narrow enveloping mucilaginous layer. Within colonies  is developed a system of parallely and radially oriented tube-like stalks,+/-  originating all from the centre of a colony; stalks are +/- thick, later widened as is the width of the cells and causing the radial lamellation of the mucilage (staining !); the stalk system lateral diffluents in the centre. Cells +/- radially elongated, joined to the ends (or within) of stalks, widely oval or slightly obovoid, in old colonies usually very densely, radially agglomerated in the peripheral layer. Cells pale blue-green or yellowish, in 5 species with aerotopes (obligatorily or facultatively).','komárek (1992)',NULL,0,0),(463,348,'description','Colonial, thallus attached to the substrate (usually growing submersed, epiphytic on algae and waterplants, rarely epilithic); sessile, solitary cells occur only in the beginning of the life cycle, later, after repeated cell division, arise (1) 2-layered or multilayered, thick, usually rounded, hemispherical or irregularly hemispherical thalli, in which the cells are irregularly aggregated or organized more or less into short radial rows; colonies enveloped by thin, firm, colourless sheaths. Cells hemispherical or polygonal-rounded, sometimes shortly but distinctly elongate, occasionally with their own thin firm sheaths.','komárek & anagnostidis (1998)',NULL,0,0),(464,348,'description','Unicellular - colonial; cells agglomerated in colonies with densely  aggregated cells. Colonies attached to the substrate, pseudoparenchymatous,  later globose or dome-shaped, multilayered, enveloped by a common sheath;  tendency of cells to form pseudofilamentous rows; colonies circular or elongated  in outline or irregular tridimensional, later several-layered, microscopic  up to macroscopically visible (point-like). Cells subspherical, more or less  oval or polygonal-rounded, or slightly elongated in marginal parts, enveloped  by thin, colourless, usually firm mucilaginous sheath; cell content pale or bright blue-green, olive-green, greyish or reddish.','komárek (1994)',NULL,0,0),(465,342,'description','Filamentous - thallous; filaments intensely true-branched, composed from primary thicker, more or less creeping, torulous, uni-, two or polyseriate trichomes and secondary lateral ones, generally thinner and growing in erect uniseriate branches (T-type of branching) without visible sheaths. Trichomes intensely constricted at cross walls, only young branches sometimes consist in some segments of long, cylindrical cells, without constrictions at cross walls; branches not attenuated towards the ends; at the ends of secondary branches dilated terminal portions (chains of more or less rounded cells) with short, wide cells, intensely constricted at cross walls, occasionally two-seriate (after lengthwise division), called ˝pseudohormocysts˝ by original author; ˝pseudohormocysts˝ probably with narrow sheaths. Cells in old trichomes barrel-shaped, isodiametric or slightly shorter or longer than wide. Heterocytes oblong-cylindrical, intercalar, solitary, cylindrical, of different length. Akinetes develop solitary, in old parts od trichomes.','Komárek (1992)',NULL,0,0),(466,330,'description','Not published, probably corresponding with thermophilic traditional Synechococcus species from the vicinity of <i>S. lividus.</i>','Katoh et al. 2001','[353]',0,0),(467,99,'reproduction','Cell division evidently by the cross-wise, perpendicular fission. Reproduction by two- or few-celled hormogonia, differentiating terminally at the ends of branches (rather known type in the Fischerellaceae). Disintegration of filaments, after which often persist the \"chroococcoid\" groups.','komárek (1992)',NULL,0,0),(468,100,'reproduction','Cell division not described, probably by the cross-wise fission of elongated cells; reproduction probably by the disintegration of a colony.','komárek (1992)',NULL,0,0),(469,101,'reproduction','Cell division crosswise to the long axis of trichomes. Reproduction by hormogonia, which develop regularly at both ends of trichomes.','komárek (1992)',NULL,0,0),(470,104,'reproduction','Vegetative cells divide cross-wise and grow to the original size before the next division; terminal cells not capable to divide; without meristematic zones. Reproduction by trichome disintegration and by akinetes.','komárek (1992)',NULL,0,1),(471,102,'reproduction','Cells divide cross-wise and grow to the original size before the next division; without meristematic zones. Reproduction by trichome fragmentation (usually at heterocytes) and by akinetes.','komárek (1992)',NULL,0,0),(472,103,'reproduction','Cells divide cross-wise, sometimes asymmetrically, and grow to the original size before the next division; all cells capable to divide; without meristematic zones. Reproduction by trichome fragmentation and by akinetes.','komárek (1992)',NULL,0,0),(473,105,'reproduction','Cell division by binary fission in two perpendicular planes in successive generations (mainly cleavage); cells remain sometimes in groups together after division (in twos or tetrads). Reproduction by colony disintegration. In a few species facultative nanocyte production is recorded.','komárek, anagnostidis (1998)',NULL,0,0),(474,105,'reproduction','Cell division always in two perpendicular planes in successive generations; the daughter cells separate soon one from another within the colonial mucilage and grow into the original size and spherical shape before the next division. Reproduction by the disintegration of colonies, sometimes up to small groups of cells, and by solitary cells liberated from a colony.','komárek (1992)',NULL,0,0),(475,106,'reproduction','Cell division by binary fission (mainly cleavage) in one plane in successive generations, perpendicular to the longitudial cell axis; In several species the daughter cells shift immediately after the division from the longitudinal position, giving the impression of \"oblique\" or \"longitudinal\" division. In several species facultative nanocyte production has been recorded. Reproduction by fragmentation of colonies, sometimes even into solitary cells.<br>','komárek et anagnostidis (1998)',NULL,0,1),(476,106,'reproduction','Division of cells always only in one (cross) direction, perpendicular to the lengthwise axis in. successive generations; however, sometimes move the daughter cells from the long axis already during the division process, particularly in small-celled species with oval cells. Reproduction by the disintegration of colonies (sometimes to solitary cells or small groups of cells). It is known the nanocyte production in several species.','komárek (1992)',NULL,0,1),(477,107,'reproduction','Cell division crosswise, sometimes asymmetrical; all cell capable to divide. Reproduction by trichome fragmentation in few-celled (up to unicellular) immotile segments, without necridid. cells.','komárek (1992)',NULL,0,0),(478,108,'reproduction','Cell division cross-wise, perpendicularly to the long axis of a trichome, daughter cells grow more or less to the original size before the next division. All cells capable to divide with the exception of apical ones. Reproduction by fragmentation of trichomes into motile hormogonia, which separate by help of necridic cells.','komárek (1992)',NULL,0,0),(479,110,'reproduction','Cells divide cross-wise to the trichome-axis and grow into the original size before the next division; all cells capable to divide, without meristematic zones. Reproduction by hormogonia escaping from sheaths and by akinetes.','komárek (1992)',NULL,0,0),(480,109,'reproduction','Cells divide by irregular binary fission within their sheaths, in different planes in successive generations; the divided cells are liberated occasionally from splits in the firm envelopes. Within the genus were recognized three types of life cycle (probably on a subgenus or genus level); (i) Cells solitary or in small, 2-4- to few- celled colonies, enveloped only by firm sheath, which splits after cell division. (ii) Cells form many-celled clusters, enveloped by firm, more or less spherical and, on the surface, spiny sheaths; within colonies sometimes with nanocyte-like cell division; the large colonies gelatinize or disintegrate, and daughter cells are liberated with their own spiny sheaths. (iii) Irregular-shaped cells, enclosed in spiny sheaths, are localized in an amorphous gelatinous mass.','komárek et anagnostidis (1998)',NULL,0,0),(481,109,'reproduction','Cell division by irregular binary fission within sheaths, \"in two or three planes\" (after Chu, 1952), multiplication by \"vegetative division\", liberation of cells from envelopes, or by fragmentation of a colony.','komárek (1992)',NULL,0,0),(482,109,'reproduction','Aplanospores present.','Chu, 1952',NULL,0,0),(483,111,'reproduction','Cell division crosswise (transversely) to the long axis into two isomorphic daughter cells, which reach the original length before next division. Reproduction by liberation of solitary cells (planocytes?) from the ends of tube-like sheaths and by disintegration of a colony','komárek & anagnostidis (1998)',NULL,0,0),(484,111,'reproduction','Cell division always cross-wise, perpendicularly to the longer axis of cells. Multiplication through the discharge of cylindrical, feebly motile planocytes from the open ends of tubular sheaths. ','Komárek (1992)',NULL,0,1),(485,112,'reproduction','Cell division cross-wise to the trichome axis, multiplication by fragmentation of trichomes.','Komárek (1992)',NULL,0,0),(486,114,'reproduction','Reproduction by the cross-wise cell division, all cells capable to divide. Trichomes divide between vegetative cells without necridia, after they reach a distinct length (usually only with several cells). Trichome fragments immotile (hormocytes), isopolar, germinate at both ends.','komárek (1992)',NULL,0,0),(487,121,'reproduction','Cell division in branches mainly crosswise, less lengthwise (before branching and sometimes before heterocyte formation), in basal parts usually irregularly in more directions. Reproduction by terminal hormogonia (2- up to 20-celled) differentiating from the ends of branches, and by terminally liberating monocytes.','komárek (1992)',NULL,0,0),(488,117,'reproduction','Cell division cross-wise, perpendicularly to the trichome axis. Reproduction by hormogonia or hormocytes.','komárek (1992)',NULL,0,0),(489,116,'reproduction','Cell division cross-wise, in meristematic zones. Reproduction by hormogonia, fhich fragmentate from branches after separation of terminal hairs.','komárek (1992)',NULL,0,0),(490,120,'reproduction','Cell division perpendicularly to the long axis of trichomes (subapical meristematic zones). Trichomes disintegrate into hormogonia in the upper part with the help of necridic cells. Reproduction by hormogonia, which develop by a special manner: in their middle develop one or two heterocytes, which separate two fiillments one from another and change into basal heterocytes.','Komárek (1992)',NULL,0,0),(491,118,'reproduction','Reproduction by hormogonia: fragmentation of trichomes by necridic cells or without necridic cells, but by formation of special lamellae between divided cells.','fiore et al. (2007)',NULL,0,0),(492,119,'reproduction','Cell division perpendicularly to the long axis of trichomes (probably always without subapical meristematic zones). Trichomes disintegrate at heterocytes and separately develop in new trichomes. Reproduction by motile hormogonia, which divide from the trichome, but help of the necridic cells and liberate from the sheath after separation of the terminal hair; hormogonia of several species with aerotopes (in all species 7; maybe an intergeneric feature).','Komárek (1992)',NULL,0,0),(493,122,'reproduction','Cell division starts by the transverse (horizontal) binary fission, in which the first division plane is perpendicular to the longer (vertical) axis of the polarized cell; later the upper (distal) part of the original mother cell divides spatially, successively or almost simultaneously, while the basal (proximal) part remains undivided. This division type results in more small daughter cells (exocytes) differentiated within the upper part of the mother sheath. After their liberation from the sheath (pseudovagina) the basal part is able to grow into the form of the original mother cell again (or divides later into two or four cells). This process is sometimes repeated. Rarely complete cell division occurs. Reproduction by liberated exocytes, which attach again to the substrate. In a few isolated strains, the cells do not grow (in agar cultures or in liquid medium) attached in the typical position, but the type of heteropolar division is retained.','komárek & anagnostidis (1998)',NULL,0,0),(494,122,'reproduction','Reproduction by asymmetrical cell division: cells firstly divide perpendicularly to the long (vertical) axis of the cell, later the apical part divides successively (or almost simultaneously) in different planes into several daughter cells (exocytes), which liberate from the pseudovagina by the apical opening. Rarely divides the whole cell into daughter cells. The upper (\"fertile\") part of the cell can separate from the \"basal\" part and divide into the exocytes several times.','komárek (1992)',NULL,0,0),(495,115,'reproduction','Cell division perpendicularly to the trichome axis. Reproduction by solitary cells and by hormogonia, which differentiate<br> at the ends of branches.','komárek(1992)',NULL,0,0),(496,123,'reproduction','Cell division always asymmetric, crosswise near the apex; the separated daughter cells (exocytes) are liberated from opened sheaths or are attached to the empty pseudovagina (origin of shrub-like or layered colonies) or remain in the common colonial mucilage (origin of gelatinous colonies with radially oriented cells). Reproduction by the liberation of exocytes from mother cells or from colonies.','komárek & anagnostidis (1998)',NULL,0,0),(497,123,'reproduction','Cells divide by_the crosswise fission, usually asymmetrically_near the apex ; sometimes develop the apical daughter cells (exocytes) repeatedly in a rapid sequence and form apical chains of exocytes. The cell division at the apical end can repeat several times. Exocytes are motile and join to the end of opened pseudovaginae or separate completely from the mother cell and attach to the substrate.','komárek (1992)',NULL,0,1),(498,125,'reproduction','Cell division irregularly in one to three or more planes. Reproduction by liberation of solitary cells from a thallus (sometimes after rupture of the sheath), of groups of two or more cells, or by short, few-celled hormogonia. Hormogonia composed of small cylindrical cells, which enlarge and become spherical during further development.','komárek (1992)',NULL,0,0),(499,126,'reproduction','Cell division crosswise, perpendicularly to the trichome, commonly occur meristematic zones. Reproduction by hormogonia (with torulous cells ?).','komárek (1992)',NULL,0,0),(500,124,'reproduction','Cell division in three perpendicular planes (less frequently irregularly), but occasionally repeatedly in one plane (origin of rows); cells more or less attain the original size (not always the original shape) before the next division. Nanocytes described in one species (C. microcystoides), but they arise from the successive division of cells without remaining in a common sheath (revision !). Reproduction by solitary cells or groups of cells, resulting from the fragmentation of colonies into several-celled mucilaginous clusters.','komárek & anagnostidis (1998)',NULL,0,0),(501,124,'reproduction','Cell division by binary fission in one or several (?) planes (sometimes probably in different directions in successive generations, but with one plane of division predominating). Reproduction not described, probably by clusters of cells enveloped by gelatinous sheaths. Little known genus, still of uncertain taxonomic status.','komárek & anagnostidis (1998)[sub lithocapsa]',NULL,0,0),(502,124,'reproduction','Cells divide in three or more planes in successive generations and grow more or less into the original size (not shape) before the next division. There were described also planocyte and nanocyte formations (relation to the family Xenococcaceae ?). Reproduction usually by the fragmentation of colonies into several-celled mucilaginous clusters','komárek (1992)',NULL,0,1),(503,124,'reproduction','Cell division probably in more directions, but with prevailing one plane of division in successive generations. Reproduction not described, probably by clusters of cells.','komárek (1992)[sub lithocapsa]',NULL,0,1),(504,113,'reproduction','Cell division crosswise, perpendicularly to the long trichome axis, in a rapid sequence. Reproduction by differently long, usually short, motile hormogonia, which separate from the trichome by help of necridic cells and liberate later from sheaths; separation of hormogonia, which remain within sheaths, causes the development of polytrichal filaments and a special type of false branching. The whole trichome sometimes disintegrates into hormogonia up to solitary cells.','Komárek (19892)',NULL,0,0),(505,127,'reproduction','Cells divide irregularly (in various planes), successively by binary fission and retain usually their irregular shape during the cell cycle; mother cells divide often into daughter cells of different shape and size. Some cells later change into baeocytes (or only some of the cells in a colony); baeocytes few or many, of different number in various species. Waterbury &amp; Stanier (1978) have never found motile baeocytes in Chroococcidiopsis, but this phenomenon does appear temporarily, being dependent on environmental factors (e. g., Andersen, in litt.). Divided cells or single cells sometimes are liberated from irregularly split mucilaginous envelopes (sheaths). Sheaths sometimes gelatinize. Different types of cell division and baeocyte production (large variability) were described by Geitler &amp; Ruttner (1935, fig.12) and Friedmann (1961, fig. 25).','komárek & anagnostidis (1998)',NULL,0,0),(506,127,'reproduction','Division of enlargeded cells by different modes: (i) successively in different planes in succeeding generations (the daughter cells do not grow in this case usually into original shape and size before next division with the exception of liberated cells; within sheath occur then sometimes daughter cells of different size); (ii) by successive or almost spontaneous irregular cell division (multiple fission) into immotile nanocytes, which liberate from the enveloping sheath by an opening (or combined with gelatinization of sheaths). Reproduction by liberated daughter cells of by clusters of ensheated cells.','komárek (1992)',NULL,0,0),(507,128,'reproduction','Cell division irregularly in more pmnes in successive generations, sometimes without growing into the original size and shape. Daughter cells within one group (from one mother cell) are often of different size. Another type of cell division: from large cells arise sometimes 8-16(32) nanocytes.','komárek (1992)',NULL,0,0),(508,129,'reproduction','Irregular cell division in different planes in successive generations, sometimes with later prevailing division in one plane (formation of pseudofilaments); enlarged cells divide occasionally into large numbers (-64) of nanocytes, which liberate by an opening from mother enveloping sheath.','komárek (1992)',NULL,0,0),(509,131,'reproduction','Light, TEM and SEM micrographs indicate that isolate 5.2 s.c.l reproduces by binary fission in either one or two successive planes at right angles. ... Isolate 5.2 s.c.l does not exhibit extensive vegetative binary fission following generation of baeocytes, a trait characteristic of the genus <i>Chroococcidiopsis </i>[31]. Additionally, isolate 5.2.s.c.l is quite morphologically distinct from filamentous <i>Microcoleus</i>.','Brown et al. (2005)',NULL,0,0),(510,130,'reproduction','Division of cells in three directions perpendicular each to another in first successive generations, later more or less irregular (in other directions); daughter cells grow more or less into the original size before the next division, but not always into the original shape. Daughter cells form usually soon their own gelatinous envelopes. Multiplication by the disintegration of colonies, sometimes up to solitary cells.','komárek (1992)',NULL,0,0),(511,132,'reproduction','Cell division by successive transverse division in the apical part or (very rarely?) along the whole length of the cell (exocyte formation). Exocytes (motile) more or less spherical or slightly elongate, separate from the apical cell end solitary or in a cluster, and attach again to the substrate. The basal remnant of the mother cell develops often into a new mother cell.','komárek & anagnostidis (1998)',NULL,0,0),(512,132,'reproduction','Cells divide firstly asymmetrically in their apical parts, later successively or almost spontaneously, always perpendicularly to the long axis of a cell, forming sometimes a row of daughter cells (exocytes) at the apical end, from which they liberate and join again to the substrate; sometimes remains the basal part of the cell undivided and further divisions proceed successively only in the upper part of the cell. The basal sterile part can again grow and again to divide at its apical end. Rarely divides the whole elongated cell into daughter cells - exocytes. The young cellsdevelop firstly with rounded apex, only later form the apical mucilaginous strings.','komárek (1992)',NULL,0,1),(513,133,'reproduction','Cell division in two planes,more or less perpendicular to one another; cells separate from one another soon after division. Reproduction by colony disintegration. <br> Komárek (1992):Cell division by binary fission in two perpendicular planes, perpendicularly to the plane of the colony. Colony disintegration.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(514,138,'reproduction','Cell division evidently by the cross-wise, perpendicular fission. Reproduction by few-celled hormogonia, which separate at the ends of branches.','komárek (1992)',NULL,0,0),(515,136,'reproduction','Cell division in two planes in successive generations, perpendicular one to another and more or less so to the colonial surface. Reproduction by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(516,136,'reproduction','Cell division in two directions in successive generations, perpendicular to each other and to the surface of the colony; the daughter cells separate one from another and grow into the original spherical shape and size before the next division. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,1),(517,135,'reproduction','Cell division by fission probably in two perpendicular planes in successive generations; reproduction probably by disintegration of colonies. <br> Komárek (1992): Reproduction by “cell division” and \"division of colonies\".','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(518,137,'reproduction','Cell division cross-wise to the long axis of a trichome. Meristematic zones (?). Reproduction by the hormogonia, liberating from sheaths; probably disintegrate by help of necridic cells.','Komárek (1992)',NULL,0,0),(519,139,'reproduction','Cell division cross the daughter cells grow more or less into the original size before the next division. Reproduction by hormogonia, which separate from the mother trichome without help of necridic cells, but sometimes with special separating discs.','komárek (1992)',NULL,0,0),(520,143,'reproduction','Cells divide evidently in various planes in successive generations and grow more or less into the original size before the next division. Reproduction by fragmentation of thallus in small groups of cells or in solitary cells. Monotypic genus.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(521,143,'reproduction','Cells divide evidently in various planes in successive generations grow more or less into the original size before the next division. Reproduction by fragmentation of thallus in small groups of cells or in solitary cells.','Komárek (1992)',NULL,0,0),(522,145,'reproduction','Cell division by binary fission (obligatory by pinching ?),transverse to the long axis, resulting in two isomorphic daughter cells. Cells grow into the original shape and size before the next division.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(523,145,'reproduction','Reproduction by the simple binary transverse fission, perpendicularly to the long axis of the cell.','komárek (1992)',NULL,0,1),(524,144,'reproduction','Cell division by binary fission (pinching), transversely to the longer cell axis, resulting in two isomorphic, rarely asymmetric daughter cells. Cells grow into the original shape and size before the next division. ','Komárek &amp; Anagnostidis 1998',NULL,0,0),(525,144,'reproduction','Reproduction by the simple binary transverse fission, repeatedly perpendicularly to the long axis of the cell. Cells grow into the original size before the next division.','Komárek (1992): ',NULL,0,0),(526,146,'reproduction','Reproduction by cylindrical, uniserial hormogonia with several up to more than 20 cells, which separate from the ends of branches, and by a special type of unicellular monocytes (called by Hoffmann 1991 as phragmocytes); phragmocytes arise by the fragmentation of a part of lateral branch under the apical cylindrical hormogonium in solitary cells; sometimes the whole branch disintegrates with except of some basal cells and the cells corresponding to the apical meristematic zone (hormogonium); phragmocytes liberate simultaneously at the apex of lateral branches after the separation of the apical hormogonium. The development of new trichomes and filaments from phragmocytes and hormogonia was not observed.','komárek (1992)',NULL,0,0),(527,147,'reproduction','Cells divide by binary fission in one plane in successive generations, transversely to the longitudinal axis, often where the ring-like precipitations are located. Reproduction by disintegration of colonies. Monospecific genus.<br>','komárek & anagnostidis (1998)',NULL,0,0),(528,147,'reproduction','Cell division by binary fission, perpendicularly to the longer cell axis. After division remain daughter cells sometimes connected for a short time (with remaining iron-oxid precipitates}, later separate one from another. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,0),(529,134,'reproduction','Cell division in two planes in successive generations, perpendicular one to another and more or less to the colonial surface; reproduction by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(530,134,'reproduction','Division of cells in two directions in subsequent generations, perpendicular to each other and to the surface of the colony. Old colonies disintegrate in small subcolonies up to solitary cells.','komárek (1992)',NULL,0,1),(531,150,'reproduction','Cell division only by rapid successive multiple fission, resulting in numerous, spherical baeocytes, which are liberated from the sheath (pseudovagina) through a rupture at the cell apex; cell division in various planes, but the first plane is always \"vertical\", from the apex to the base. Baeocytes grow to the mother cell size before the next division (i.e. several times larger than baeocytes). Reproduction only by non-motile baeocytes, which attach to the substrate.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(532,150,'reproduction','Reproduction by the rapid successive up to simultaneous total division of cells (multiple fission) into more small daughter cells (nanocytes). The first division proceeds in the cells perpendicularly to the substrate (special type?) or +/- irregulary, further division planes are irregular. Immotile nanocytes escape through the apical or subapical openings in the pseu- dovagina. All cells divide obligatory only once into small nanocytes, which grow after joining to the substrate again into the original size and shape before the next division. Very rarely remains the \"basal\" nanocyte within the mother pseudovagina','Komárek (1992)',NULL,0,1),(533,155,'reproduction','Cell division changes in three or more planes, later mostly in one plane (origin of short rows); cells later shift within colony and again divide in more planes. Reproduction by disintegration of colonies and by the liberation of solitary cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(534,155,'reproduction','Ability of cell division in 3 or more planes, perpendicularly to each other, but the repeated division perpendicularly to one axis of a row prevails in later generations; the cells grow into the original size after their division and before the next binary fission, but<br> not into the original shape. Reproduction by colony desintegration.','Komárek (1992)',NULL,0,0),(535,156,'reproduction','Cells divide by binary fission, transversely to their longitudinal axis and perpendicularly to the colonial surface, always in one plane in successive generations. Cells reach the original size before the next division. Reproduction by disintegration of colonies. Monotypic genus.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(536,156,'reproduction','Cell division only in one direction in successive generations, perpendicular to the longer axis of the cell. The colonies disintegrate into small cell groups up to solitary cells','Komárek (1992)',NULL,0,1),(537,151,'reproduction','Cell division in different planes in the basal parts of thallus, later in pseudofilaments cross-wise, perpendicularly to the axis of pseudofilaments. The apical spherical cells divide into nanocytes. Reproduction by liberated nanocytes.','komárek (1992, sub geitleriella)',NULL,0,0),(538,154,'reproduction','Cell division only in the transverse plane, perpendicular to the longer axis of slightly elongate cells, in one plane in successive generations. Reproduction by fragmentation of colonies.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(539,154,'reproduction','Cell division (pinching) repeatedly only ion one crosswise direction, perpendicular to the one (longer) axis of cells in successive generations. Reproductions by the disintegrations of colonies.','Komárek (1992)',NULL,0,0),(540,153,'reproduction','Cell division always in one plane in successive generation more or less perpendicularly to the mucilaginous strands; hemispherical divided cells grow to the original shape before the next division. Reproduction by disintegration of colonies.','Komárek &amp; Anagnostidis (1998)',NULL,0,1),(541,153,'reproduction','Division of cells (pinching) in one and the same plane in successive generations, perpendicularly to the longer axis of cells (and usually also to the axis of a mucilaginous string). After division the cells separate from each other a distance of up the the length of one cell. The development of a three-dimensional colony starts from a short pseudofilament. Reproduction by the disintegration of colonies.','Komárek (1992)',NULL,0,1),(542,157,'reproduction','Reproduction by simultaneous or successive (from the apex) differentiation of exocytes in the upper part of the cylindrical cells, rarely along the whole cell; cell division by transverse fission. Exocytes separate one by one, or a great part of a cell is transformed into a row of exocytes; they are liberated terminally from the mother cell end, become attached by their long sides to the substrate, change their polarity and grow into a new cell from an upper side.','komárek & anagnostidis (1998)',NULL,0,0),(543,157,'reproduction','Reproduction by exocytes, which different-late by the rapid successive (or almost spontaneous ?) crosswise fission of cell ends; they remain usually for a distinct period joined to the mother cell as rows of small cells, later separate, join to the substrate by their side, change their polarity and grow from the upper side into the new ,cylindrical cell (Geitler 1960).','komárek (1992)',NULL,0,1),(544,149,'reproduction','One of the main generic diagnostic features is the longitudinal cell division into two parts, not transverse as in great majority of coccoid Cyanobacteria. Longitudinal cell division is characteristic of the genera from the group of <i>Woronichinia-Gomphoshaeria, Snowella</i>.','Hindák (2002)',NULL,0,0),(545,158,'reproduction','Cell division at first horizontal, i.e. perpendicular to the vertical axis, later in further directions, by<br> binary fission; the upper part divides after separation of the upper-outer part of a cell simultaneously by multiple fission or by successive (up to 3) binary fissions into many (to 32 or more) small, rounded baeocytes (to 5 um in diameter), which escape from the sheaths into the environment, become attached to the limestone and penetrate again into the substrate. The «apical» large cells divide usually only lengthwise by binary fission, rarely both lengthwise and crosswise; (fig. 587).','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(546,158,'reproduction','Cell division at first perpendicularly to the vertical or horizontal axes, or in more directions, by binary fission, later (after separation of the upper-outer part of a cell), the upper part divides spontaneously in many (up to 32 or more) small, rounded nanocytes (up to 5 um ), which escape from the sheaths into the environment, attach to the limestone and penetrate again into the substrate.','Komárek (1992)',NULL,0,0),(547,152,'reproduction','Cell division (binary fission) irregular, in more planes in successive generations, but in pseudofilaments prevails the crosswise division to the pseudofilaments. Nanocytes not observed. Reproduction probably by the clusters of several cells.','komárek (1992)',NULL,0,0),(548,159,'reproduction','Cell division irregular in three, later different planes; daughter cells do not reach the original form before next division; nanocytes (or baeocytes) always lacking. Reproduction by the liberation of cells or groups of cells from sheaths.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(549,159,'reproduction','Division of cells firstly in three directions perpendicular each to other in successive generations, later slightly irregular; each daughter cell divide later more or less in three perpendicular planes, but the daughter cells remain gathered to packett-like sarcinoid formations. Nanocytes are absent. Multiplication by the disintegration of colonies.','komárek (1992)',NULL,0,1),(550,163,'reproduction','Cell division by binary fission, in the same plane in successive generations, perpendicular to the longitudinal axis; cells sometimes diverge from one another slightly after division and reach the original size and shape before next fission. Reproduction by disintegration of colonies. Monotypic genus.','komárek & anagnostidis (1998)',NULL,0,0),(551,163,'reproduction','Cell division only crosswise, perpendicularly to the long axis of a cell. Reproduction by disintegration of colonies. ','Komárek (1992)',NULL,0,1),(552,161,'reproduction','Cell division in two or more planes in successive generations, perpendicular to one another, later irregularly (successive binary fission); reproduction by solitary cells and by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(553,161,'reproduction','Cell division firstly in two directions by binary fission from which increase the Chroococcus-like group of cells, later also irregularly in more planes. Reproduction by the disitegration of colonies.','komárek (1992)',NULL,0,1),(554,167,'reproduction','Cell division irregular in three or more planes, in endolithic pseudofilaments mostly transverse, but sometimes lengthwise to the axis of pseudofilaments. In pseudofilaments division occurs in both intercalary and apical cells. Sometimes there is division into baeocytes m epilithic pseudofilaments by successive cell division. Reproduction by solitary cells, baeocytes, or by small gelatinous clusters of cells.','Komárek & Anagnostidis (1998)',NULL,0,0),(555,167,'reproduction','Cell division irregular in different planes, in endolithic pseudofilaments mostly crosswise to the axis of pseudofilaments. Sometimes production of nano- cytes by successive cell division. Reproduction by solitary cells (nanocytes) or by small gelatinous clusters with cells','komárek (1992)',NULL,0,1),(556,166,'reproduction','Cells divide cross-wise and grow more or less into the original size before the next division. Without meristematic zones, all cells capable to divide. Reproduction by trichome fragmentation into hormogonia and by akinetes.','komárek (1992)',NULL,0,0),(557,162,'reproduction','Cell division into two equal parts, in two perpendicular planes in successive generations; reproduction by fragmentation of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(558,162,'reproduction','Cell division in two perpendicular. planes in successive generations; the cells remain joined together in 2-4-8-32-celled colonies, later desintegrate in smaller colonies up to in solitary cells.','komárek (1992)',NULL,0,1),(559,169,'reproduction','Reproduction by successive multiple fission of cells into baeocytes; first cell division always horizontal, perpendicular to the long vertical. axis, later in various planes. Baeocytes numerous, usually several times smaller than the original mother cell.','Komárek &amp; Anagnostidis (1998): ',NULL,0,0),(560,169,'reproduction','Reproduction by the rapid successive, total division of cells (multiple fission) into more small daughter cells (nanocytes). The first or several first division planes are oriented parallel with the substrate (perpendicularly to the vertical axis of the sessile cell). Immotile nanocytes escape from the pseudovagina through the apical opening. All cells divide obligatory only once into small nanocytes, which grow after joining to the substrate again into the +/- original size and shape (before the next division).','komárek (1992)',NULL,0,0),(561,164,'reproduction','Cells always divide by binary fission (cleavage) into two morphologically equal, hemispherical daughter cells, in one plane, which is perpendicular to the longer cell axis in successive generations. Cells grow to the original size and shape before the next division takes place. Reproduction by cell division and succeeding separation of daugther cells.','komárek & anagnostidis (1998)',NULL,0,0),(562,164,'reproduction','Reproduction by the cell division, perpendicular to one (longer) axis of the cell into two morphologically identical semiglobular daughter cells, which grow up to the original shape before the next division; the cells_divide repeatedly in only one plane in the succeeding generations.','komárek (1992)',NULL,0,1),(563,175,'reproduction','Cells divide in three or more planes in successive generations and reach approximately the original size before the next division. The rows of cells originate probably by the prevalence of cell division in one plane. Reproduction mainly by small colonies or gelatinous groups of cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(564,175,'reproduction','Cells divide in three or more planes in successive generations and grow more or less into the original size before the next division. The rows of cells arise probably by the prevailing cell division in one plane. Reproduction mainly by small colonies or groups of cells.','Komárek (1992)',NULL,0,1),(565,170,'reproduction','Cells divide irregularly in three or more planes in basal parts, and usually crosswise in erected trichomes, with numerous lateral divisions. Reproduction by planocytes, which separate from terminal parts of trichomes and liberate from sheaths, and by free clusters of several cells enveloped by mucilaginous envelopes.','komárek (1992)',NULL,0,0),(566,176,'reproduction','Cell division by transverse binary fission into two equal daughter cells, perpendicularly to the long axis. Reproduction by the disintegration of compound and single colonies, even into unicellular fragments.','Komárek &amp; Anagnostidis (1998)',NULL,0,1),(567,176,'reproduction','Division of cells only perpendicular to their longer axis; daughter cells separate soon one from another. Reproduction by the disintegration of colonies in mucilaginous clusters with several or solitary cells','komárek (1992)',NULL,0,1),(568,173,'reproduction','Cells divide crosswise or lengthwise (before the branching). Reproduction by hormogonia. usually 5-15-celled, which arise on the ends of short branches, and probably by fragments of thallus.','komárek (1992)',NULL,0,0),(569,174,'reproduction','Cell division (according to Voronichin´s orig. fig:) by binary fission (pinching), in one direction in successive generations, perpendicular to the longer axis (origin of radial rows); reproduction by disintegration of colonies.','Komárek &amp; Anagnostidis 1998',NULL,0,0),(570,174,'reproduction','Cell division-by pinching, only in one plane, perpendicular to the longer axes of cells. Reproduction by liberating small daughter colonies or by gelatinous clusters containing several cells.','Komárek (1992): ',NULL,0,1),(571,177,'reproduction','Cells divide irregularly in basal parts of thallus and more or less crosswise in the upper pseudofilaments. Reproduction by liberation of solitary cells from the thallus and, probably, by the disintegration of thallus.','komárek (1992)',NULL,0,0),(572,180,'reproduction','Reproduction by uniserial hormogonia, which seprate from ends of branches; they are usually morphologically very distinct (different from other cells in branches) and contain aerotopes (liberation usually during humid vegetation periods).','komárek (1992)',NULL,0,0),(573,181,'reproduction','Reproduction by hormogonia, which are usually club-shaped (clavate), cylindrical or only slightly constricted at cross-walls, with cells morphologically distinguishable from cells in trichomes, sometimes with aerotopes; the whole short branches, or ends of long branches (like in Fischerelm species) change usually in hormogonia. Hormogonia escape from the ends of sheaths.','komárek (1992)',NULL,0,0),(574,178,'reproduction','Cells in basal parts divide in various planes, apical cells sometimes divide into baeocytes. Still a problematic and not revised monotypic genus.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(575,179,'reproduction','Cells divide regularly in three perpendicular planes in successive generations without displacement of daughter cells (this type of division causes development of regular cubic colonies); cells grow into the original spherical form before next division. Reproduction by colony disintegration.','komárek & anagnostidis (1998)',NULL,0,0),(576,179,'reproduction','Division of cells regularly in three directionsin succeeding generations, perpendicularly to each other. Cells grow into the original size and shape before next division. Reproduction by the disintegration of a colony.','komárek (1992)',NULL,0,0),(577,182,'reproduction','Cell division cross-wise, perpendicularly to the long axes of trichomes; in old trichomes apical meristematic zones. Trichomes disintegrate at heterocytes. Reproduction by hormogonia, which separate from trichomes by necridic cells and by akinetes.','komárek (1992)',NULL,0,0),(578,184,'reproduction','Cell division crosswise or lengthwise (before true branching). Reproduction by hormogonia (fractured segments of filaments).','Komárek (1992)',NULL,0,0),(579,171,'reproduction','Division of cells perpendicularly to the long axis of a trichome (sometimes meristematic zones), disintegration of trichomes at intercalar heterocytes before false branching. Reproduction by hormogonia, which divide from trichomes by help of necridic cells after separation of the terminal hair.','komárek (1992)',NULL,0,0),(580,185,'reproduction','Cell division transverse, more or less in the middle or in the upper part of a cell (asymmetrically displaced towards the apex), rarely two divisions occur almost simultaneously. The liberated, usually elongate apical daughter cell becomes: attached to the substrate by either end. ','komárek & anagnostidis (1998)',NULL,0,0),(581,185,'reproduction','Cell division perpendicularly to the longer axis of cells, usually asymmetrically in their upper part, rarely in the middle. The upper daughter cells (exocytes) liberate from the sessile part and attach by one end again to the substrate; very rarely separate two exocytes almost simultaneously.','komárek (1992)',NULL,0,0),(582,186,'reproduction','Cell division by the crosswise binary fission, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable to divide with the exception of apicalones. Reproduction by motile hormogonia, which separate without help of necridic cells or by fragmentation of whole trichomes.','komárek (1992)',NULL,0,1),(583,187,'reproduction','pinkish. Cell division by binary fission (mainly byp inching) into two morphologically equal, hemispherical daughter cells, which reach the original globular shape before next division; cells always divide into two perpendicular planes in successive generations.','Korelusová et al. (2009)',NULL,0,0),(584,188,'reproduction','Cells divide crosswise to the axis of a trichome. Reproduction probably by the trichome disintegration.','komárek (1992)',NULL,0,0),(585,191,'reproduction','Cell division irregularly in various planes in successive generations. Reproduction by liberation of divided and ensheathed cells from ruptured mother sheaths. Nanocyte production rarely observed in several species (?). Occasional presence of enlarged resting cells with thick, firm and usually intensely coloured envelopes.','komárek & anagnostidis (1998)',NULL,0,0),(586,191,'reproduction','Cell division in different directions in succeeding generations, the cells do not grow into the oriminal form before the next fission. Occasiollally division into spherical nanocytes (˝Aphanocapsa˝ or ˝Gloeocapsa˝ - status). Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,0),(587,189,'reproduction','Cell division by simple binary transverse fission, perpendicular to the long axis of the cell. Reproduction<br> probably by liberation of solitary ensheathed cells or small groups of cells. ','komárek & anagnostidis (1998)',NULL,0,1),(588,189,'reproduction','Reproduction by the simple binary transverse fission, perpendicularly to the long axis of cells.','komárek (1992)',NULL,0,1),(589,193,'reproduction','Cell division perpendicularly to the long axis of a trichome, usually in meristematic zones. Reproduction by disintegration of trichomes within colonies and, particularly, by hormogonia, differentiating after the separation of the apical hair by help of necridic cells, and sometimes liberating from old colonies. Division of colonies.','komárek (1992)',NULL,0,0),(590,194,'reproduction','Cell division crosswise to the long axis of a trichome. Reproduction by the disintegration of trichomes in hormocytes.','komárek (1992)',NULL,0,0),(591,195,'reproduction','Cell division in two planes in successive generations, perpendicular to one another and to the colony surface; the daughter cells divide completely in the later period of a cell cycle. Reproduction by the colony disintegration.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(592,195,'reproduction','Cell division in two directions in subsequent generations, perpendicular to each other and to the surface of the colony; the daughter cells remain after division joined together, forming the ˝cordiform˝ cells. Reproduction by the disintegration of colonies.','Komárek (1992)',NULL,0,1),(593,192,'reproduction','Cell division transverse to the longitudinal axis, in one plane in succesive generations; cells grow in the original size and shape before next division; they produce their own envelopes just after division. Reproduction by disintegration of colonial aggregates and (in several species) by the liberation of cells after gelatinization of envelopes. Nanocyte production recorded in a few species.','komárek & anagnostidis (1998)',NULL,0,1),(594,192,'reproduction','Cell division (binary fission) crosswise, perpendicularly to the long axis of elongated cells in successive generations; the daughter cells separate soon one from another and produce immediately their own mucilaginous envelopes; cells grow into the original size and shape before the next division, but also the production of nanocytes was sporadically observed. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,1),(595,197,'reproduction','Reproduction is performed asexually by binary division.','Margheri et al. (2008)',NULL,0,0),(596,190,'reproduction','Cell division by binary fission within gelatinous envelopes, in three perpendicular planes in successive generations; daughter cells shift in mucilage irregularly and produce their own gelatinous envelopes soon after division (= formation of lamellate sheaths). Cells grow to the original size and shape before next division (difference from Chroococcaceae). Reproduction by liberation of groups of cells or solitary cells (with or without envelopes) from the colonial mass and by disintegration of colonies into small gelatinous clusters containing several cells. In some species is known nanocyte production. Aphanocapsa-stages (with diffluent sheaths, resulting in arrangement of cells in more or less homogeneous slime) and resting stages (cells enveloped by thick, firm sheaths, incorrectly designated as ˝akinetes˝ = ˝Dauerzellen˝) develop under unfavourable conditions.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(597,190,'reproduction','Cell division in three perpendicular planes in successive generations; the daughter cells soon separate one from another after division, they develop their mucilaginous envelopes and grow into the original spherical - shape and size before the next division. Reproduction by disintegration of colonies into small cell clusters or into solitary cells with narrow gelatinous envelopes. It is known the nanocytic cell division. The described akinetes are probably only resting stages with dense mucilaginous envelopes, caused by environmental, unfavourable conditions (status, ecomorphoses), not real akinetes as known in filamentous cyanophytes.','komárek (1992)',NULL,0,1),(598,200,'reproduction','Cells divide crosswise to the trichome axis, characteristic are the terminal meristematic zones. Reproduction by separated branches or hormogonia, which germinate at both sides, but later (after formation of heterocytes); they change in heteropolar growth.','komárek (1992)',NULL,0,1),(599,198,'reproduction','Cells divide cross-wise, particularly<br> in subapical meristematic zones. Reproduction by hormocysts or by fragmentation of filaments.','komárek (1992)',NULL,0,0),(600,203,'reproduction','Cell division by symmetrical cross-wise binary fission, cells grow into the original size before the next division. Reproduction by motile hormogonia, liberating from the apical part of trichomes by help of necridic cells (?). Hormogonia join by one end to the substrate and germinate at the opposite end.','komárek (1992)',NULL,0,0),(601,199,'reproduction','Cells divide cross-wise, without meristematic zones. Reproduction by hormogonia, separating from trichomes (usually ends of branches) by help of necridic cells.','komárek (1992)',NULL,0,0),(602,202,'reproduction','Cells divide irregularly in different planes and remain joined together in irregular packets','komárek (1992)',NULL,0,0),(603,204,'reproduction','Cells divide cross-wise, sometimes a little oblique and irregular, or length-wise before branching. At the ends of branches develop terminal hormogonia, liberating from sheaths through the apical opening. Hormogonia uniserial, composed from short cells, intensely constricted at cross walls.','komárek (1992)',NULL,0,0),(604,201,'reproduction','Cells divide cross-wise in trichomes, in old parts sometimes successively in more planes into numerous nanocytes,<br> liberating from enveloping sheath. Hormogonia formation not observed','komárek (1992)',NULL,0,0),(605,206,'reproduction','Cells divide irregularly in various planes, in pseudofilaments with predominant crosswise binary fission. After division, they separate soon from one another and produce their own sheaths. Reproduction by solitary cells (monocytes) which are liberated from the mucilaginous sheaths in the upper part of pseudofilaments, or by small gelatinous clusters of several cells. Baeocytes not observed (even not in culture).','komárek & anagnostidis (1998)',NULL,0,0),(606,206,'reproduction','Cells divide irregularly in different planes, in pseudofilaments with prevailing crosswise binary fission. After division, they separate soon one, from another and produce their own sheaths. Reproduction by solitar cells (monocytes) which liberate from the mucilaginous sheaths, or by small. gelatinous clusters of several cells. Nanocytes not observed.','Komárek (1998)',NULL,0,1),(607,205,'reproduction','Crosswise cell division by symmetric binary fission, only in special parts of a trichome (unclear or distinct meristematic zones - generic feature 7); cells grow into the original size before the next division (always 7). Reproduction by disintegration of an upper part of a trichome into motile hormogonia, after the separation of the hair. Hormogonia attach by one end to the substrate and germinate at the other ones.','komárek (1992)',NULL,0,0),(608,209,'reproduction','Cell divison (binary fission) crosswise, perpendicularly to the long axis of cells, in one and the same plane in successive cell cycles. Daughter cells soon separate one from another and form their own gelatinous envelopes, widened to the basis of a stalk. Reproduction by the disintegration of colonies and liberation of solitary cells.','komárek (1992)',NULL,0,0),(609,208,'reproduction','Reproduction was not described. Cells divide evidently cross-wise along the whole trichome, reproduction probably by hormogonia.','komárek (1992)',NULL,0,0),(610,211,'reproduction','Cell division crosswise; daughter cells grow more or less into the original size before the next division. Reproduction by motile hormogonia; fragmentation of trichomes by help of necridic cells.','komárek (1992)',NULL,0,0),(611,210,'reproduction','Cell division in various planes in successive cell cycles, but the crosswise binary fission prevails in marginal parts or in surface layers of colonies. Typical nanocytes not observed. Reproduction by solitary cells or by small clusters of cells. Not a well known genus, almost all the species must be revised; data about Hydrococcus from saline waters and mineral lakes are still uncertain.','Komárek &amp; Anagnostidis (1998): ',NULL,0,0),(612,210,'reproduction','Cell division in different planes in successive cell cycles, in marginal or erected rows prevails the cross-wise binary fission. Typical nanocytes not observed. Reproduction by solitary cells or by small clusters of cells.','komárek (1992)',NULL,0,0),(613,207,'reproduction','Cell division crosswise, with all cells capable to divide. Reproduction by the division of trichomes, proceeding regularly by help of special sacrified cells like discs; trichomes disintegrate along the total length, sometimes up to solitary cells. Hormocytes germinate at both ends (isopolar).','komárek (1992)',NULL,0,0),(614,215,'reproduction','Cells divide perpendicularly to the trichome axis, probably along the whole length with exception of a hair (no meristematic zones were recorded). Reproduction by hormogonia, liberating from the thallus.','komárek (1992)',NULL,0,0),(615,212,'reproduction','Cells divide cross-wise by binary fission; without meristematic zones, all cells capable to divide. Reproduction probably by hormogonia','komárek (1992)',NULL,0,1),(616,212,'reproduction','Reproduction was not described. Cells divide evidently cross-wise along the whole trichome, reproduction probably by hormogonia.','Komárek (1992) sub <i>Hormothamnion</i>',NULL,0,1),(617,213,'reproduction','Cells divide by binary fission, irregularly in various planes, in pseudofilaments crosswise (perpendicularly to the long axis of pseudofilament), before branching also lengthwise or obliquely. Oldest cells near the substrate surface often change into baeocytes, which arise after rapid successive or almost simultaneous repeated cell division (multiple fission). Reproduction by baeocytes, rarely by liberation of solitary small cells (?).','komárek & anagnostidis (1998)',NULL,0,0),(618,213,'reproduction','Cells divide irregularly in different planes, in boring pseudofilaments mainly crosswise. Enlarged cells divide sometimes in nanocytes, usually in the surface parts of thallus. Reproduction by nanocytes and by solitary cells, surrounded by gelatinous envelopes; they divide irregularly and the pseudofilaments differentiate soon from them.','komárek (1992)',NULL,0,0),(619,216,'reproduction','All cells capable to divide, cell division crosswise, perpendicularly to the trichome axis. Reproduction by short hormogonia (sometimes disintegrating up into solitary cells) and by akinetes.','komárek (1992)',NULL,0,0),(620,214,'reproduction','All cells capable to divide in different planes, in filaments usually mainly perpendicularly to the trichome-axis. Terminal cells of branches divide often repeatedly in nanocytes. Reproduction by nanocytes which liberate from the opened sheaths at the ends of filaments and branches, by solitary liberated cells (sometimes with own envelopes) and by fragments of filaments (rarely by hormogonia).','komárek (1992)',NULL,0,0),(621,217,'reproduction','Cells divide crosswise, particularly in indistrict, short, meristematic zones. Reproduction by hormogonia, which separate from trichomes by help of necridic cells.','komárek (1992)',NULL,0,0),(622,218,'reproduction','Cell division by the crosswise binary fission, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable to divide. Reproduction by the fragmentation of trichomes without necridic cells into immotile hormocytes (indistinct motility was not proved yet).','komárek (1992)',NULL,0,1),(623,219,'reproduction','Cell division in one plane, perpendicular to the longitudinal axis of pseudofilaments (i. e., transversely to the longer axis of cells); reproduction by disintegration of pseudofilaments and by facultative liberation of solitary cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(624,219,'reproduction','Cell division only in one plane in succeeding generations, always cross-wise to the axis of pseudofilaments, i.e., cross-wise to the shorter axis of cells. Reproduction probably by fragmentation of pseudofilliments.','komárek (1992)',NULL,0,1),(625,220,'reproduction','Cells divide by the crosswise fission, all cells capable to divide (but sometimes within short division zones), with the exception of apical ones. Division of trichomes in more or less constant distances, by a help of a special intercellular discs (special sacrified cells ?). Fragmented trichomes remain sometimes chain-like connected by their ends, by rests of intercellular discs. Reproduction by a total disintegration of trichomes. Hormocytes germinate at both ends (isopolar).','komárek (1992)',NULL,0,0),(626,222,'reproduction','Cell division crosswise. Reproduction by hormogonia. Trichomes divide and separate usually at the tops of loops (without connection with heterocytes) and the ends of divided trichomes grow and later form new attenuated trichome ends.','Komárek (1992)',NULL,0,0),(627,224,'reproduction','Cell division by transverse binary fission into two equal parts, perpendicular to the longer cell-axis, in one plane in successive generations. Cells become more or less the original size before the next division. They soon separate from one another after division and usually shift to the parallel position; rarely remaining in short rows. Reproduction by «budding» of daughter spherical colonies from the surface of the old mother colony, or by disintegration of colonies into small clusters of cells or even solitary cells.','komárek & anagnostidis (1998)',NULL,0,0),(628,224,'reproduction','Cell division always perpendicularly to the lengthwise axis of elongated cells, in one and the same plane in successive generations; however, the daughter cells soon shift from the original direction and form groups with parallely situated cells. Colonies reproduce by the ˝budding˝ of small daughter colonies, or by disintegration of colonies into small groups of cells enveloped by slime, up into solitary cells.','komárek (1992)',NULL,0,0),(629,221,'reproduction','Cell division perpendicularly to the longer trichome axis, cells grow into the original shape and size before the next division. Reproduction by disintegration of trichomes without necridic cells; trichomes disintegrate regularly +/- in their middle after they reach a distinct length. Hormocytes germinate at both sides (isopolar).','komárek (1992)',NULL,0,0),(630,226,'reproduction','Reproduction by 8-10- celled hormocyst, which separate at the ends of branches. Sheaths of hormocysts thick, usually brownish. Hormogonia not known. Aerophytic, known mainly from flower-pots in glass-houses.','komárek (1992)',NULL,0,0),(631,223,'reproduction','Cells divide by symmetrical, crosswise binary fission, cells grow into the original size before next division. Reproduction by immotile hormocytes which adhere lengthwise by their sides to the substrate and grow up at both poles. Hormocytes liberate from trichomes in their apical parts without help of necridic cells.','komárek (1992)',NULL,0,0),(632,225,'reproduction','Cells divide by +/- symmetrical (rarely asymmetrical) crosswise binary fission, cells grow into original size before next division. Reproduction by motile (?) hormogonia, liberating from trichomes at their ends, fragmentated without help of typical necridic cells, but sometimes after death of sacrifying cells.','komárek (1992)',NULL,0,1),(633,227,'reproduction','Reproduction by nanocytes and monocytes (probably immotile), which arise at the ends of branches; monocytes differentiate usually in rows. Hormogonia and akinetes not known.','komárek (1992)',NULL,0,0),(634,165,'reproduction','Cells divide cross-wise (sometimes asymmetrically) and grow more or less into the original size before the next division. Without meristematic zones all cells capable to divide. Reproduction by trichome fragmentation and by akinetes.','komárek (1992)',NULL,0,0),(635,230,'reproduction','Cell division by binary fission, probably only in one plane in successive generations, perpendicular to the length of the strands. Reproduction possibly by liberation of solitary cells. Insufficiently known monospecific genus.','komárek & anagnostidis (1998)',NULL,0,0),(636,230,'reproduction','Cell division probably only in one plane, more or less perpendicular to the axis of strings. Reproduction not described, probably by liberated solitary cells or small clusters of cells in mucilaginous envelopes.','komárek (1992)',NULL,0,0),(637,232,'reproduction','Cells divide evidently crosswise, reproduction was not described, hormogonia were not observed.','komárek (1992)',NULL,0,0),(638,228,'reproduction','Cell division by binary ission, in 2-3 planes in successive<br> generations. The cells reach the original spherical shape before the<br> next division. Reproduction proceeds by disintegration of colonies or liberation of cells from colonies.','komárková et al. (2010)',NULL,0,0),(639,229,'reproduction','All cells capable to divide (crosswise binary fission), daughter cells grow into the original size before next division. Reproduction by the fragmentation of trichomes without help of necridic cells, hormogonia immotile (or facultatively motile ?).','Komárek (1992)',NULL,0,0),(640,233,'reproduction','Cell division crosswise. Reproduction by 10-14-celled hormogonia, separating from ends of trichomes (branches). Hormogonia divide sometimes during germination in two (or more) segments; the first branching follows soon after germination of hormogonia.','komárek (1992)',NULL,0,0),(641,231,'reproduction','Cell division probably in one plane in successive generations. Reproduction possibly by solitary, liberated cells. Insufficiently known, monospecific genus.','komárek & anagnostidis (1998)',NULL,0,1),(642,231,'reproduction','Cells divide probably only in one plane in successive generations. Reproduction not described, probably by small groups of cells enveloped by mucilage.','komárek (1992)',NULL,0,1),(643,236,'reproduction','Reproduction by fragmentation of trichomes and by akinetes.','Komárek (2008)',NULL,0,0),(644,238,'reproduction','Cells divide crosswise or lengthwise before branching. Reproduction by trichome disintegration, hormogonia were not described.','komárek (1992)',NULL,0,0),(645,234,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, usually in a rapid sequence. Sometimes irregular meristematic zones. Reproduction by +/- short, motile hormogonia, which separate from trichomes by help of necridic cells. Disintegration of mats.','komárek (1992)',NULL,0,0),(646,235,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, daughter cells grow up to the original size before the next division. All cells capable to divide. Reproduction by motile hormogonia, which escape from the open sheaths in the periphery of a colony.','komárek (1992)',NULL,0,0),(647,239,'reproduction','Cells divide crosswise or lengthwise before branching. Reproduction by hormogonia or by disintegration of trichomes.','komárek (1992)',NULL,0,0),(648,237,'reproduction','Cells divide perpendicularly to the substrate and probably in two planes perpendicular to one another (deduced from the arrangement of cells, but according to the original diagnosis in three planes? ). Insufficiently known genus, probably with more species.','komárek & anagnostidis (1998)',NULL,0,0),(649,237,'reproduction','Cell division probably in two planes perpendicular one to another and to the substrate (formation of flat groups). Cells grow more or less up to the original size before the next division. Reproduction by liberated solitary daughter cells.','komárek (1992)',NULL,0,0),(650,240,'reproduction','Cells divide evidently crosswise and lateral before branching. Reproduction was not described, hormogonia were not observed.','komárek (1992)',NULL,0,0),(651,242,'reproduction','Cells divide crosswise and lengthwise before branching. Reproduction probably by hormogonia, which were, however, not described.','komárek (1992)',NULL,0,0),(652,243,'reproduction','Cell division (binary fission) into two equal daughter cells, in two planes perpen- dicularly to one another and to the plane of the colony in successive generations; cells do not change their alignment after division (reason for regular perpendicular , rows of cells) and reach the original size before next division. Reproduction by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(653,243,'reproduction','Cell division in two planes in successive generations, perpendicular one to another and to the plane of a flat colony. Daughter cells shift slightly one from another, but they remain in perpendicular rows in a colony. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,0),(654,241,'reproduction','Cells divide crosswise and lengthwise before branching. Reproduction by hormogonia.','komárek (1992)',NULL,0,0),(655,244,'reproduction','Reproduction by hormogonia, which separate from trichomes in apical parts. Hormogonia develop heteropolar or firstly isopolar with two central heterocytes, which shift later into the basal position.','komárek (1992)',NULL,0,0),(656,245,'reproduction','Cell division crosswise, daughter cells grow into the original size before the next division. Reproduction by motile fragments of trichomes or hormogonia; fragmentation usually by help of necridic cells.','komárek (1992)',NULL,0,0),(657,246,'reproduction','Cells divide lengthwise in two perpendicular planes in successive generations (i. e., lengthwise with the longer cell axis) and perpendicularly to the plane of colony; cells separate and slightly shift apart from one another after division. Reproduction by disintegration of colonies. During the vegetation cycle of several species there are various morphological («Synechocystis-», «Merismopedia-», typical «Microcrocis-») stages.','komárek & anagnostidis (1998)',NULL,0,0),(658,246,'reproduction','Division of cells more or less in two planes, perpendicularly one to another and to the plane of colony (i.e., lengthwise); the cells form in young colonies the perpendicular rows, later in more-celled colonies are arranged irregularly. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,1),(659,247,'reproduction','Cell division by binary fission in three perpendicular planes in regular «cubic» arrangement; cells grow into the original size and shape before next division. Reproduction by disintegration of colonies into small clusters of cells or even into&nbsp; solitary cells.','komárek & anagnostidis (1998)',NULL,0,0),(660,247,'reproduction','Cell division in three planes in successive generations, perpendicular one to another; daughter cells soon separate one from another, and grow into the original size and shape before the next division. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,0),(661,249,'reproduction','Reproduction only by crosswise cell division, always perpendicularly to the long axis of the cell; sometimes occurs the asymmetrical cell division.','komárek (1992)',NULL,0,0),(662,252,'reproduction','Cells divide irregularly, in filaments mainly crosswise. Reproduction probably by solitary liberated cells (monocytes) and possibly also by short pieces of disintegrated trichomes; hormogonia were not observed.','komárek (1992)',NULL,0,0),(663,251,'reproduction','Cells divide irregularly by binary fission in three or more planes, in older colonies often obliquely, forming groups&nbsp; of cells. In old colonies some cells occasionally (mainly in the margin) change into temporarily motile baeocytes (planocytes). Reproduction by disintegration of colonies and by baeocytes.','komárek & anagnostidis (1998)',NULL,0,0),(664,251,'reproduction','Division of cells in three or more directions in successive generations, the daughter cells do not grow into original shape of the mother cell; several cells divide in distinct phases of life cycle (under special conditions) into motile nanocytes.','komárek (1992)',NULL,0,0),(665,253,'reproduction','Cells divide by binary fission, irregularly, mainly perpendicular to the longer cell axis (origin of the cell arrangement). Reproduction by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(666,253,'reproduction','Cell division transversally and later in different planes in successive generations, forming tangentially oriented cells in a colony. The cells reach +/- their original size, but not shape before the next division. Reproduction by the disintegration of the colony.','komárek (1992)',NULL,0,1),(667,254,'reproduction','Cells divide crosswise to the trichome axis and grow into the original size before the next division, all cells capable to divide, without meristematic zones. Reproduction by hormogonia, disintegration of trichomes, and by akinetes.','komárek (1992)',NULL,0,0),(668,250,'reproduction','Cell division irregular in more planes in successive generations, in pseudofilaments, particularly at their ends, with prevailing crosswise binary fission. End cells divide occassionally into nanocytes. Reproduction probably only by nanocytes.','komárek (1992)',NULL,0,0),(669,256,'reproduction','Cells divide crosswise, sometimes in meristematic (mainly apical) zones. Reproduction mainly by hormogonia with short barrel-shaped cells; hormogonia germinate bipolar.','Komárek (1992)',NULL,0,0),(670,255,'reproduction','Cells divide crosswise. Reproduction by motile hormogonia, which differentiate from trichomes by disintegration at heterocytes, by disintegration of thallus and by akinetes, respectively.','komárek (1992)',NULL,0,0),(671,257,'reproduction','Cells divide irregularly in different planes, in rows mostly perpendicular to the growth direction; sometimes successive division in several smaller cells (monocytes ?, nanocytes ?), which are liberated from thallus and serve to the reproduction. Monotypic genus. <br>','komárek & anagnostidis (1998)',NULL,0,0),(672,257,'reproduction','Cells divide irregularly in different planes, in rows mostly perpendicularly to the growth direction; sometimes successive division in several smaller cells (nanocytes), which liberate from thallus and serve to the reproduction.','komárek (1992)',NULL,0,1),(673,261,'reproduction','Cell division not described, but probably irregular and in various planes in successive generations. Little known, unrevised, monotypic genus; the ferric precipitates can hardly be used as the only generic differential feature, in other characters similar to Chlorogloea.','komárek & anagnostidis (1998)',NULL,0,0),(674,261,'reproduction','Cell division not described, but probably<br> irregular in different planes in successive generations.','komárek (1992)',NULL,0,0),(675,258,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, in a rapid sequence. Sometimes occur irregular meristematic zones. Reproduction by +/- short, motile hormogonia, which separate from the ends or from whole trichomes by help of necridic cells.','Komárek (1992)',NULL,0,0),(676,260,'reproduction','Cell division in two planes in successive generations, perpendicularly to the surface of the colony into two equal parts. Reproduction by colony disintegration.','komárek & anagnostidis (1998)',NULL,0,0),(677,260,'reproduction','Cell division in two directions perpendicular to the surface of the colony. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,1),(678,263,'reproduction','Cells divide in more planes, but only crosswise in young trichomes and. branches. Reproduction by hormogonia, which separate from the ends of branches, by disintegration of trichomes, by planocytes and by akinetes (germination was described).','komárek (1992)',NULL,0,0),(679,262,'reproduction','Cells divide crosswise , or lengthwise (irregularly) before branching and in pseudoparenchymatous discs. Reproduction by hormogonia and liberating akinetes. Hormogonia separate from trichomes by help of necridic cells.','komárek (1992)',NULL,0,0),(680,264,'reproduction','Cell division transversely to the pseudofilament axis, or (mainly from enlarged terminal cells) successively into few or several (2-16) oval or spherical, motile baeocytes. Reproduction by means of baeocytes. Little known genus, never found again for about 70 years, needs revision.','komárek & anagnostidis (1998)',NULL,0,0),(681,264,'reproduction','Cell divide in pseudofilaments by the repeated crosswise fission and grow before the next division into the original size. Apical enlarged cells divide sometimes successively in 2-16 nanocytes, which escape from the thin, firm sheath, opened at the apex (real sporangia 7; sheaths are not visible in pseudofilaments). Nanocytes are motile, join to the substrate and change in a new basal cell, which start to divide crosswise in the upper part. One nanocyte remains sometimes joined to the pseudofilament and grows into normal vegetative cell.','komárek (1992)',NULL,0,1),(682,265,'reproduction','Reproduction by hormogonia, separating from the apical parts of trichomes.','komárek (1992)',NULL,0,0),(683,259,'reproduction','Cells divide crosswise. Reproduction probably by fragmentation of pseudofilaments (in original description is supposed the trichomal structure of pseudofilaments and fragments of pseudofilaments are described as ˝true hormogonia with conical rounded terminal cells˝,but not motile).','komárek (1992)',NULL,0,0),(684,269,'reproduction','Cell division in two equal parts. Reproduction by disintegration of colonies.','Hindák (2002)',NULL,0,0),(685,268,'reproduction','Cell division irregular, in various planes, predominantly perpendicular to the surface of a colony. Reproduction by solitary liberated cells or by mucilaginous clusters of cells. Freshwater (usually from running waters) as well as marine species (rocky littorals of seas and oceans); only one species known from Europe.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(686,268,'reproduction','Cell division irregular, probably in more planes, predominantly perpendicular to the surface of a colony. Reproduction probably by solitary liberated cells or by mucilaginous clusters of cells.','komárek (1992)',NULL,0,1),(687,267,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable of division with the exception of apical ones, sometimes indistinct meristematic zones occur. Reproduction by variously long, +/- motile hormogonia, which separate at the end parts of trichomes by help of necridic cells or by fragmentation of whole trichomes (also with necridic cells).','komárek (1992)',NULL,0,0),(688,272,'reproduction','Cell division crosswise,the cells grow to the original size before the next division. Meristematic zones irregular (?). Reproduction by trichome disintegration into hormogonia, by help of necridic cells.','Komárek (1992)',NULL,0,0),(689,270,'reproduction','Cell division by the crosswise binary fission, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable to divide. Reproduction by fragmentation of trichomes without necridic cells into immotile (?) hormogonia.','komárek (1992)',NULL,0,0),(690,275,'reproduction','Cells divide in several planes, but with predominant transverse division, perpenidicular to the long axis of the row of cells (origin of short pseudofilaments) or lengthwise; the divarication of rows is initiated by the lengthwise cell division (with respect to the axis of the pseudofliament). The smaller or narrower «basal» cells sometimes divide into baeocytes. Reproduction by baeocytes and probably also by small groups of cells, surrounded by gelatinous envelopes. Little known monotypic genus, which needs revision.','komárek & anagnostidis (1998)',NULL,0,0),(691,275,'reproduction','Cells divide in more planes, but with prevailing cross division, perpendicular to the long axis of the row of cells (short pseudofilament); the divarication of rows is initiated by the lengthwise cell division (in respect to the axis of the pseudofilament). The smaller or narrower ˝basal˝ cells divide sometimes in nanocytes. Reproduction by nanocytes and probably also by small groups of cells, enveloped by gelatinous envelopes.','komárek (1992)',NULL,0,1),(692,273,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, in a rapid sequence. Irregular meristematic zones. Reproduction by motile hormogonia, liberating and escaping from sheaths at the ends of filaments, by means of necridic cells. Hormogonia germinate end grow at both ends (isopolar development). The absence of heterocytes was hesitated by Hoffmann et Demoulin (1985); in the case of heterocyte production must be Plectonema transferred into Scytonema (Nostocales).','komárek (1992)',NULL,0,0),(693,274,'reproduction','Cells divide irregularly by binary fission in various planes, in pseudofilaments predominantly crosswise. The lengthwise division of apical cells in pseudofilaments resulting in pseudodichotomous divarication is a typical feature of the genus (fig. 610). Enlarged cells, which arise in different parts of thallus, sometimes divide into baeocytes. Reproduction bybaeocytes.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(694,274,'reproduction','Cells divide irregularly in different planes; enlarged cells from different parts of thallus divide sometimes in nanocytes. Reproduction by nanocytes.','komárek (1992)',NULL,0,1),(695,277,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable of division with the exception of apical ones (meristematic zones ?). Reproduction by variously long hormogonia (motile ?) which separate from trichomes by help of necridic cells.','komárek (1992)',NULL,0,0),(696,281,'reproduction','Cell division crosswise to the long axis of a trichome. Reproduction probably by the fragmentation of trichomes.','komárek (1992)',NULL,0,0),(697,282,'reproduction','Cell division perpendicularly to the longer trichome axis, cells grow into the original shape and size before the next division. Trichomes disintegrate (in several species up to solitary cells or few-celled segments) without necridic cells.','komárek (1992)',NULL,0,0),(698,284,'reproduction','Cell division probably only perpendicularly to the long axis of the radially oriented cells. Reproduction imperfectly described, probably by solitary cells. (Since the cell division proceeds irregularly in more than two planes, the genus belongs to the Entophysalidaceae).','komárek & anagnostidis (1998)',NULL,0,0),(699,284,'reproduction','Cell division not described, probably predominantly perpendicularly to the longer axis of radially oriented cells, or sometimes irregularly. Reproduction not described.','komárek (1992)',NULL,0,1),(700,285,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable to divide, but the indistinct meristematic zones arise. Reproduction by intense and common fragmentation of trichomes into motile hormogonia or immotile hormocytes (7), usually by help of necridic cells.','komárek (1992)',NULL,0,0),(701,287,'reproduction','Reproduction by hormogonia, which develop from the apical ends of radially arranged filaments. The cells divide in young germinating hormogonia in different planes (origin of basal disc).','komárek (1992)',NULL,0,0),(702,288,'reproduction','Cells divide within thallus irregularly, in pseudofilaments predominantly crosswise in one plane in successive generations. Baeocytes differentiate by simultaneous or successive cell divisions of apical cells. Reproduction by baeocytes, many per cell, and later liberated from the colony. From about ten described species, several are satisfactorily characterized, however, only one (the type species) is known from Europe.','komárek & anagnostidis (1998)',NULL,0,0),(703,288,'reproduction','Cells divide within thallus irregularly, in pseudofilamentous rows predominantly in one plane in successive generations. Large apical and subapical cells often divide in great amount of nanocytes. Reproduction probably by nanocytes.','komárek (1992)',NULL,0,1),(704,283,'reproduction','Cell division successively in three or more different planes (mainly radially in colonies); cells do not grow to the original, more or less spherical form before the next division. Nanocytes always lacking.','komárek & anagnostidis (1998)',NULL,0,0),(705,283,'reproduction','Division of cells in three perpendicular planes in successive generations in the beginning, later divide more or less radially in the colony, without the divided cells having grown into the original spherical shape, but growing more or less into the original size. Multiplication by the disintegration of colonies.','komárek (1992)',NULL,0,0),(706,286,'reproduction','The cell division crosswise, the daughter cells grow into original size before the next division. Reproduction by hormogonia,<br> liberating from the ends of trichomes; hormogonia of different length (up to 16-celled), but also short. Probably also reproduction by solitary cells<br> (planocytes or monocytes ?).','komárek (1992)',NULL,0,0),(707,289,'reproduction','Cells divide transversely in one plane in successive generations, in later stages perpendicularly<br> to the radiating rows. Reproduction by disintegration of mucilaginous colonies.','komárek & anagnostidis (1998)',NULL,0,0),(708,289,'reproduction','Cells divide crosswise in one plane in consequent generations and the daughter cells remain after division often longer time near one to another. Reproduction by the disintegration of colonies.','komárek (1992)',NULL,0,1),(709,294,'reproduction','Cell division transversely to the longitudinal axis, in the same plane in successive generations. Reproduction probably by the liberation of solitary cells. The classification into the Entophysalidaceae or Hydrococcaceae (near Cyanodermatium) is possible, considering the structure of colonies and basal cells (see also Bourrelly 1970).','komárek & anagnostidis (1998)',NULL,0,0),(710,294,'reproduction','Cells divide only crosswise, perpendicularly to the longer axis, only in one place in consequent generations. Reproduction probably by solitary cells.','komárek (1992)',NULL,0,1),(711,295,'reproduction','Cells divide crosswise. Reproduction by disintegration of trichomes, typical hormogonia not observed','komárek (1992)',NULL,0,0),(712,292,'reproduction','Cells only divide transversely to the longer axis, symmetrically or asymmetrically; daughter cells sometimes remain joined together in short pseudofilamentous rows. Reproduction by disintegration of colonies.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(713,292,'reproduction','Cell division (binary fission) by cleavage, always perpendicular to the longer axis of cells, in involution cells sometimes irregularly (asymmetrically). Daughter cells separate one from another, or form short pseudofilamentous rows. Reproduction by disintegration of colonies and by solitary cells.','komárek (1992)',NULL,0,1),(714,296,'reproduction','Cell division perpendicularly to the long axis of a trichome, later in meristematic zones. Reproduction by disintegration of trichomes whithin colonies and heterocytes and by hormogonia, separating after the separation of the hair by the help of necridic cells and sometimes liberating from the colonies.','Komárek (1992)',NULL,0,0),(715,293,'reproduction','Cell division by binary fission, transverse to the long axis into two more or less isomorphic daughter cells; the cells separate from one another before the next division. Reproduction by disintegration of colonies.','komárek & anagnostidis (1998)',NULL,0,0),(716,293,'reproduction','Cell division (binary fission) in two, perpendicularly to the longer axis of cells, in the middle of cells or slightly excentrically in involution cells. Cells separate soon one from another. Reproduction by disintegration of colonies and by solitary cells.','komárek (1992)',NULL,0,0),(717,297,'reproduction','Cell division by symmetrical (under suboptimal conditions asymmetrical) crosswise binary fission, always perpendicularly  to the longer axis of cells; daughter cells grow +/- to the original size before next division. All cells capable to divide. Reproduction by the easy trichome fragmentation up to solitary cells within enveloping mucilage, without necridic cells, and by the disintegration of mucilaginous clusters with solitary cells or by trichome fragments.','Komárek (1992)',NULL,0,0),(718,297,'reproduction','',' Komárek (1970: 358)','[324]',0,0),(719,297,'reproduction','Überwinternde Zustände sind einzelne Zellen in Gallerthüllen im Benthos der Wasserbehälter. Im Frühjahr beginnen die Zellen zu wachsen, verlängern sich und teilen sich entweder in zwei oder mehrere Zellen auf einmal. In diesem Zustande gelangen sie ins Plankton. In den ersten Stadien bilden sie einzelne, ziemlich lange, kontinuite, verdrehte Fäden, welche jedoch sehr bald in Teiltrichome zerfallen. Die Schnelligkeit<br> der Zellteilung ist sehr ungleichmässig auch in demselben Teiche. Ich beobachtete auch in einer Population Typen, wo sich die Zellen in zwei ziemlich lange Tochterzellen teilten, und umgekehrt Trichome, die sich auf einmal in einige kurze Zellen teilten. Beim Zerreissen des Trichomes bleiben beide Enden beieinander, event. verschieben sich etwas infolge des weiteren Wuchses, oder sie biegen sich; später entstehen Kolonien, die aus mehreren mehrzelligen Trichomen zusammengesetzt sind, aneinander mit ihren Enden angeschlossen. In diesem Zustand überdauert <i>R. elegans</i> den längsten Teil der Vegetationszeit, bis sie in einzelne Zellen auf den Grund sinkend zerfällt. Der Beginn und das Ende der Vegetation ist ziemlich allmählich. Hochproduktionen und Wasserblüten bildet sie nicht. Die Vegetation dauert vom<br> VI. bis IX., schwache Maxima entstehen im VII. bis VIII., meist erscheinen sie jedoch nur sporadisch. Sie vegetiert in der Regel gemeinsam mit planktischen chlorokokkalen Algen, beziehungsweise auch Kieselalgen (z. B. <i>Melosira granulata</i>), anderen Blaualgen und Cryptomonaden.','Komárek (1958: 161-162)',NULL,0,1),(720,298,'reproduction','Reproduction occurs by transverse binary fission in a single plane.','Choi et al. (2008)',NULL,0,0),(721,299,'reproduction','Cells divide perpendicularly to the lengthwise trichome axis (meristematic zones ?). Reproduction probably by hormogonia.','komárek (1992)',NULL,0,0),(722,300,'reproduction','Cell division crosswise to the trichome axis, without meristematic zone; all cells capable to divide. Reproduction by motile hormogonia, which separate from trichomes probably without help of necridic cells.','komárek (1992)',NULL,0,1),(723,302,'reproduction','Cells divide crosswise to the trichome axis, mainly in meristematic zones near the ends of branches. Reproduction by hormogonia, which develop at the ends of branches and liberate from sheaths. Hormogonia germinate at both ends and form isopolar filaments.','komárek (1992)',NULL,0,0),(724,303,'reproduction','Cells divide crosswise to the trichome axis. Reproduction by hormogonia, which separate from the filament by help of necridic cells, liberate from the sheath and germinate at both ends.','komárek (1992)',NULL,0,0),(725,306,'reproduction','Cells divide irregularly, usually in three or various planes in successive generations (development of «stigonematoid˝ thallus), but in apical parts or in sides of thallus with predominating crosswise fission (development of rows of cells). Reproduction by solitary cells or groups of cells with their own gelatinous envelopes; solitary cells (motile monocytes, planocytes) escape from the splitting envelopes at the marginal and apical parts of thallus (after which remain the cup-shaped remnants of sheaths). Resting stages (cells enveloped by firm sheaths) were also described.','komárek & anagnostidis (1998)',NULL,0,0),(726,306,'reproduction','Cells divide irregularly, usually in three or more planes in successive generations (development of ˝stigonematoid˝ thallus), but in apical parts of thallus or in its sides with prevailing crosswise fission (development of rows of cells). Reproduction by solitary cells or groups of cells enveloped by gelatinous envelopes or by solitary cells (motile planocytes), which escape from the splitting envelopes at the marginal and apical parts of thallus (after which remain the cup-shaped rests of sheaths). The resting stages (cells enveloped by firm sheaths) were also described.','komárek (1992)',NULL,0,0),(727,308,'reproduction','Cell division crosswise, perpendicularly to the long axis of trichomes. Reproduction by motile hormogonia, separating from trichomes by help of necridic cells (?).','komárek (1992)',NULL,0,0),(728,310,'reproduction','Cell divison crosswise to the lenth of trichomes. Reproduction probably by disintegration of trichomes up to solitary cells.','komárek (1992)',NULL,0,0),(729,304,'reproduction','Cell division mainly crosswise, sometimes asymmetrically. Reproduction by 8-10- celled hormogonia, which separate serially from the ends of branches by help of necridic cells, by hormocytes (short ensheathed branches) and by solitary cells, clusters or 2-celled groups of cells, originating from the disintegrating old trichomes.','komárek (1992)',NULL,0,0),(730,305,'reproduction','Cells divide probably crosswise. About reproduction is nothing known (hormogonia ?) .','komárek (1992)',NULL,0,0),(731,311,'reproduction','Cell division in various planes, apical or subapical (rarely lateral or basal) cells (endolithic, near the surface of rocks and stones) sometimes divide into several to numerous baeocytes. Reproduction by baeocytes and small clusters of cells enveloped by mucilage (?).','komárek & anagnostidis (1998)',NULL,0,0),(732,311,'reproduction','Cell division in different planes, apical cells sometimes divide into nanocytes. Reproduction by nanocytes and small clusters of cells enveloped by mucilage.','komárek (1992)',NULL,0,1),(733,307,'reproduction','Cell division in two perpendicular planes in successive generations, reproduction by colony disintegration.','komárek & anagnostidis (1998)',NULL,0,0),(734,307,'reproduction','Cell division into two equal parts by binary fission, in two planes in successive generations, perpendicularly to each other and to the surface of the colony; the cells grow into the original size and shape before the next division. Multiplication of colonies by their disintegration in two or more parts.','komárek (1992)',NULL,0,0),(735,309,'reproduction','Cell division in two directions in successive generations, perpendicular to each other and to the surface of a colony; soon after division the cells separate one from another in distant positions. The colonies disintegrate into small cell groups up to solitary cells.','komárek (1992)',NULL,0,0),(736,313,'reproduction','Cell division on two planes in successive generations.','Azevedo et Sant\'Anna (2003)',NULL,0,0),(737,312,'reproduction','Cell division crosswise, without distinct meristematic zones. Reproduction by hormocysts, which separate solitary or in rows from ends of branches, 8- or more-celled, with firm, thick sheaths. Hormogonia not known.','komárek (1992)',NULL,0,0),(738,316,'reproduction','Cell division crosswise, perpendicularly to the long axis of a trichome, daughter cells grow +/- up to the original size before the next division. All cells capable to-divide. Reproduction by fragmentation of trichomes into motile hormogonia without necridic cells.','komárek (1992)',NULL,0,0),(739,317,'reproduction','Cell division only by multiple fission, more or less simultaneously or in rapid sequence in various directions, resulting in numerous spherical, motile baeocytes (planocytes), which liberate from the split or gelatinized sheaths. Small baeocytes reach the original size (several times larger than baeocytes) before the next multiple fission. Reproduction only by baeocytes.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(740,317,'reproduction','Reproduction by the almost spontaneous total cell division (multiple fission) into many small daughter cells (nanocytes); nanocytes are motile (planocytes), and escape from the firm, layered sheath through an irregular opening. All cells divide obligatory only once into nanocytes, which grow into the +/- original size and shape before the next division.','komárek (1992)',NULL,0,1),(741,319,'reproduction','Cells divide in different planes in basal trichomes and pseudoparenchymatous mass, but mainly crosswise in erected branches. Reproduction by solitary monoaytes (planocytes ?), which liberate from the end of branches after opening of the sheath, rarely from intercalar cells. Hormogonia and hormocysts not known.','komárek (1992)',NULL,0,0),(742,318,'reproduction','Cell division crosswise, reproduction by fragmentation, sometimes in short pieces up to solitary cells.','komárek (1992)',NULL,0,0),(743,322,'reproduction','Cell division crosswise to the trichome length. Reproduction by hormogonia, separating from ends of branches.','komárek (1992)',NULL,0,0),(744,321,'reproduction','Cells divide in all planes, but the crosswise fission is mostly common in trichomes. Meristematic zones occur only in sections, in which hormogonia arise. Reproduction by hormogonia, which liberate from the ends of trichomes and branches, morphologically different from trichomes (more cylindrical, uniseriate); hormogonia two- or more-celled, rarely many-celled.','komárek (1992)',NULL,0,0),(745,290,'reproduction','Reproduction by disintegration of trichomes.','komárek (1992)',NULL,0,1),(746,320,'reproduction','Cell division by repeated binary fission, transverse to the longer (vertical) axis into a row of more or less short cylindrical or discoidal exocytes, liberating at the apex from the opened sheath (pseudovagina); separated exocytes in pseudofilaments are able to divide repeatedly. The exocytes are attached to the substrate by one end (of the elongated exocyte) and grow into a new cell along the original exocyte long axis. (According to special cytology and biology probably a special cyanoprokaryotic type.)','komárek & anagnostidis (1998)',NULL,0,0),(747,320,'reproduction','Cell division always only perpendicularly to the long axes of the attached individuals; first division is more or less asymmetrical, dividing the upper part from the basal cell; then the upper exocyte(s) grow continually and divide successively (the formed exocytes divide repeatedly within´the mother sheath); this process results into a row of exocytes forming the pseudofilament. Single exocytes or their clustered groups (in S. indicus) liberate from the open sheath at the free, apical end. Exocytes are polarized, join to the substrate by the one end (in comparison with the orientation within the mother sheath) and start to grow at the opposite apical end.','komárek (1992)',NULL,0,0),(748,329,'reproduction','Cells divide crosswise. Reproduction only by solitary cells (monocytes), liberating from open sheaths, hormogonia or hormocysts not known.','komárek (1992)',NULL,0,0),(749,327,'reproduction','Cell division by binary fission (mainly by pinching) into two morphologically equal, hemispherical daughter cells, which reach the original globular shape before next division; cells always divide in two perpendicular planes in successive generations. If the mucilaginous envelopes are formed around cells, they split together with dividing cells.','komárek & anagnostidis (1998)',NULL,0,0),(750,327,'reproduction','Cell division (pinching) always in two perpendicular planes in successive generations (recognizable only on solid substrates); daughter cells separate soon after division and grow into the oriminal size and shape before next binary fission. Reproduction by solitary cells.','komárek (1992)',NULL,0,0),(751,323,'reproduction','Cell division crosswise to the trichome length. Reproduction by (3-13-celled) hormocysts, which arise at the ends of branches, solitary or up to four in series; cells in hormocysts wider than in branches, constricted at cross walls; during the germination of hormocysts, the single heterocytes usually develop (both heteropolar or isopolar germlings arise).','komárek (1992)',NULL,0,0),(752,326,'reproduction','Cells divide by binary fission, transversely (always in one plane in successive generations, perpendicular to the longitudinal axis) into two isomorphic or different (after asymmetric binary fission) daughter cells, which occasionally remain joined for longer period in pairs (obligatory by cleavage ?). Reproduction by cell division; (fig. 127).','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(753,326,'reproduction','Cell division (pinching or cleavage) always by binary fission, perpendicular to the longer axis of the cell, i.e., in the same plane in successive generations; daughter cells grow more or less in the original size before the next division. After division the cells separate or remain arranged in short rows (pseudofilaments) of several cells, freely connected with their ends. Under suboptimal conditions arise the elongated filamentous involution cells, which are able to divide asymmetrically. Reproduction by solitary cells.','komárek (1992)',NULL,0,1),(754,324,'reproduction','Cells divide crosswise to the trichome axis. Reproduction by hormogonia.','komárek (1992)',NULL,0,0),(755,331,'reproduction','Cells divide evidently crosswise to the trichome long axis. Reproduction not described, probably by hormogonia.','komárek (1992)',NULL,0,0),(756,332,'reproduction','Cells divide crosswise to the trichome axis, with subterminal meristematic zones. Reproduction by hormogonia, Which germinate at both ends, but after heterocyte formation (usually in pairs) change in heteropolar growth.','komárek (1992)',NULL,0,0),(757,335,'reproduction','Cell division perpendicularly to the long axis of a trichome. Reproduction by hormogonia, which separate from trichomes at heterocytes, and by the germination of akinetes. Disintegration of mats.','komárek (1992)',NULL,0,0),(758,339,'reproduction','Cells divide crosswise to the trichome axis, or longitudinally before branching. Reproduction by trichome disintegration and by akinetes.','komárek (1992)',NULL,0,0),(759,334,'reproduction','Cell division by the crosswise fission of all cells, with exception of apical ones. The cells grow into original size before the next division. Reproduction by fragmentation of trichomes into motile hormogonia by help of necridic cells and by disintegration of colonies. Hormogonia germinate at both ends (isopolar).','komárek (1992)',NULL,0,0),(760,342,'reproduction','Cells divide in different planes in old trichomes, and mainly crosswise in branches. Reproduction by solitary monocytes (planocytes ?), which liberate from ˝pseudohormocysts˝, and from old, torulous trichomes and branches.','Komárek (1992)',NULL,0,0),(761,338,'reproduction','Cells divide by symmetric binary fission with very different division frequencies on a trichome and during the vegetation phase; all cells capable to divide. Reproduction by fragmentation of trichomes into non-motile hormocytes.','komárek (1992)',NULL,0,0),(762,337,'reproduction','Cell division transverse, in the same plane in successive generations, perpendicular to the longitudinal axis; reproduction by solitary cells liberated from gelatinous tubes. Monospecific genus.','komárek & anagnostidis (1998)',NULL,0,0),(763,337,'reproduction','Division only in one plane perpendicular<br> to the long axis of cells. Reproduction by solitary cells escaping from the open sheaths at their apexes.','komárek (1992)',NULL,0,1),(764,340,'reproduction','Cells divide evidently crosswise to the trichome, with the exception of branching. Reproduction not described (hormogonia ?).','komárek (1992)',NULL,0,0),(765,343,'reproduction','Cells divide in the trichome perpendicularly by binary fission; all cells (including apical) are able to divide, without meristematic zones; disintegration of trichomes into immotile segments, without ecridic cells. Phylogenetic similarity is about 90% against the Geitlerinema and 87.7-96.9 % to the nearest Phormidium clusters (Fig. 2). -','strunecký et al. (2011)',NULL,0,0),(766,341,'reproduction','Cell division only crosswise to the trichome axis. Reproduction by hormogonia, which separate by help of necridic cells from ends of branches and obligatory by 2-12-celled hormocysts, which can develop serially at the terminal parts of branches.','komárek (1992)',NULL,0,0),(767,345,'reproduction','Cell division only transversely to the longitudinal axis, in the same plane in successive generations; reproduction by fragmentation of pseudofilaments and liberation of cells from sheaths (planocytes).','komárek & anagnostidis (1998)',NULL,0,0),(768,345,'reproduction','Cell division by the crosswise fission, reproduction by fragmentation of pseudofilaments or by liberation of solitary cells from the open envelopes, which are motile (planocytes).','komárek (1992)',NULL,0,0),(769,347,'reproduction','Cells divide irregularly in two or more different planes, but usually perpendicular to the substrate; divided cells separate from one another or remain closed in a common sheath. Occasionally in solitary cells occurs successive baeocytic division into numerous baeocytes, which are liberated from the enveloping sheaths by their splitting or gelatinization. The baeocytes differentiate from the whole mother cell, or the cell first divides into two parts by more or less horizontal binary fission and only one (upper) part divides into baeocytes.','komárek & anagnostidis (1998)',NULL,0,0),(770,347,'reproduction','Division of cells irregular, more or less perpendicularly to the substrate; cells do not grow into original shape before the next division. From cells arise sometimes nanocytes, which serve to the reproduction.','komárek (1992)',NULL,0,1),(771,344,'reproduction','Cells divide only by crosswise binary fission. Reproduction by hormogonia.','komárek (1992)',NULL,0,0),(772,348,'reproduction','Cells divide by binary fission in various planes forming spatially layered aggregations. Occasionally some marginal or surface cells divide into baeocytes. Reproduction by baeocytes which escape from split sheaths, and by solitary cells (ensheathed?).','komárek & anagnostidis (1998)',NULL,0,0),(773,348,'reproduction','Division of cells irregular, in more directions perpendicularly to the substrate, but later crosswise (parallely to the´substrate) or obliquely; cells grow or do not grow in the original size before next division. From some cells (usually in marginal parts of colonies) arise sometimes nanocytes (reproduction cells).','komárek (1994)',NULL,0,0),(774,349,'reproduction','Cell division crosswise to the length of trichomes. Reproduction probably by disintegration of trichomes and colonies.','Komárek (1992)',NULL,0,0),(775,346,'reproduction','Cell division in two planes perpendicular to one another in successive generations, and perpendicular to the colony surface; reproduction by disintegration of colonies and especially by liberation of solitary cells (sometimes spontaneously) from the colony (expulsingcells).','komárek & anagnostidis (1998)',NULL,0,0),(776,346,'reproduction','Cell division in two directions in successive generations, perpendicular to each other and to the surface of the colony, immediately after division separating from one another. Reproduction by the disintegration of colonies and by the liberation of solitary cells (sometimes by their almost spontaneous ˝expulsion˝) from the colony (mainly at the end of the life cycle or in stress situations).','komárek (1992)',NULL,0,0),(777,141,'reproduction','','Komárek et al. (2010)','[131][132]',0,0),(778,98,'eco_distro','The single species is know from calcareous rocks of the tide zone of the Adriatic Sea coast (Dalmatia). A little know genus.','komárek (1992)',NULL,0,0),(779,99,'eco_distro','The type species is the single member of this genus; it grows among other cyanophytes or on the surface of their thallus in slightly thermal, alkalic springs in the Yellowstone National Park (U.S.A.). A little known genus.','komárek (1992)',NULL,0,1),(780,100,'eco_distro','All 5 species were described from one polluted concrete basin near Vienna (Austria), and they were not proved again. Very unclear genus, maybe bacteria.','komárek (1992)',NULL,0,0),(781,101,'eco_distro','The type species (<i>A. normannii</i>) occurs sporadically in periphyton and metaphyton on water plants in clear and cold streaming waters and in littoral of clear, unpolluted lakes. Localities are known allover the world, but the taxonomic identity of all floristic data is not clear. One species was described from a spring in Georgia (USSR), the another one from thermal springs in the Yellowstone National Park (U.S.A.).','komárek (1992)',NULL,0,0),(782,104,'eco_distro','Almost all species are planktic, sometimes forming characteristic water blooms, the most known type species (<i>A. flos-aquae</i>) is important in managed fish ponds and in lakes; mainly are distributed in eutrophic water reservoirs, few species are halophilic. All species have limited areas of distribution (and possess characteristic species ecology), several species are described as endemites (e.g., from Caspian Sea).','komárek (1992)',NULL,0,1),(783,102,'eco_distro','Planktic species, sometimes forming water blooms (mainly from the subg. <em>Dolichospermum</em>) or in mats covering different substrates, water plants, submersed woods, stones etc. Several species grow benthic or in soils, several are known from salinic (brackish) biotopes. Many species have limited geographic areas of distribution.','Komárek (1992)',NULL,0,0),(784,103,'eco_distro','Planktic species forming sometimes water blooms, rarely occur in metaphyton of small water bodies with submerse vegetation and in paddy fields (the non-planktic species need revision). Mainly distributed in tropical and subtropical regions, but occur commonly also in summer seasons in warmer areas of temperated zones. Several species prefer alkalic and highly mineral or salinic waters.','komárek (1992)',NULL,0,0),(785,105,'eco_distro','Majority of species grows in periphyton, benthos and metaphyton of stagnant and streaming freshwater biotopes (usually with clear water, common in lakes), several species are known from the sea littoral (psammon, periphyton), thermal springs, or from subaerophytic or submerse endolithic biotopes. Very characteristic species grow subaerophytically on wet rocks and walls or among mosses in moors and peaty bogs. Planktic species need the revision. (type of cell division). Distributed allover the world, but several species are ecologically sharply limited and occur in geographically limited areas of distribution.','komárek (1992)',NULL,0,0),(786,106,'eco_distro','Widely distributed genus with species, limited usually by very specific ecological conditions. They live epipelic in stagnant waters (<i>A. stagnina, A. nidulans</i>), in soils (<i>A. pallida</i>), subaerophytic on wet rocks and walls (<i>A. castagnei, A. caldariorum, A. saxicola</i>), several fine species are planktic (<i>A. minutissima, A. brevis,</i> or <i>A. elabens</i> with facultatively developed aerotopes), and several characteristic species were described from salinic environments (<i>A. halophytica, A. rubra</i>, etc.). <i>A. bullosa</i> and <i>A. thermicola</i> are known from thermal springs.','komárek (1992)',NULL,0,1),(787,107,'eco_distro','The single known species, <i>A. africanum</i>, grows in wet, salinic places (drying pools) in desert areas (Libya, Kuwait) below the surface of sandy substrate. Probably more species exist with different ecology.','komárek (1992)',NULL,0,0),(788,108,'eco_distro','Several species are benthic in freshwater biotopes (<i> A. jenneri</i>, <i>A. platensis</i>, etc.), several are planktic, mainly in tropical and salinic (mineral) lakes and water reservoirs (<i>A. maxima</i> , <i>A. fusiformis</i>), and used as important biotechnological organisms for mass culture (usually under the<br> incorrect name ˝<i>Spirulina platensis˝</i> ). Few species are known from marine littoral biotopes (<i>A. funiformis</i> ).','komárek (1992)',NULL,0,0),(789,108,'eco_distro',' Plantae hydrophilae aut halophilae, nunquam terrestres.','Gomont (1892)',NULL,0,0),(790,110,'eco_distro','Mainly metaphytic species, growing in not polluted water reservoirs, usually among or on submerse water plants, or benthic. Several species are important members of the microflora in paddy fields (<i>A. fertilissima</i>). Almost all species grow in geographically limited areas of distribution, mainly in tropical regions (special ecology).','komárek (1992)',NULL,0,0),(791,109,'eco_distro','All species subaerophytic, known from wet rocks in China (Szechwan, Anhui), Nepal and India (the Himalayas), Japan and probably also from central America. genus, several species could be possibly the status resting of Gloeocapsa or Gloeocapsopsis (comp. also the genus Endospora). If the genus is definable, it comprises probably more species occurring mainly in aerophytic localities in SE Asia.','komárek (1992)',NULL,0,0),(792,111,'eco_distro','All five described species are from metaphytic and periphytic habitats in freshwater. Two species are known from thermal springs (Copeland, 1936; Fremy, 1949).','komárek (2003)',NULL,0,0),(793,111,'eco_distro','The different species occur in periphyton and metaphyton of special biotopes (thermal springs, alkalic tropical swamps). A little known genus','Komárek (1992)',NULL,0,1),(794,112,'eco_distro','Aerophytic, known only from limestone walls of one cave in Hungary. A little known species.','Komárek (1992)',NULL,0,0),(795,114,'eco_distro','The different species occur in periphyton and metaphyton of clear, mainly small freshwater water bodies with water plants (three species), epiphytically (endogloeic) in the mucilage of other freshwater algae (1), benthic in lakes (1) or aerophytic on calcareous substrates (2). Known mainly from the Europe, the type species B. trilocularis has probably cosmopolitan distribution (but it is not common).','komárek (1992)',NULL,0,0),(796,121,'eco_distro','The type species was described from Europe, later found in various places all over the world including tropical countries, but recently not confirmed; it occurs attached to water plants, stones and submersed wood in swamps and on wet rocks (identity of all these samples is not doubtless). Another species was described from Brasil (epiphytic on <i>Stigonema </i>and <i>Batrachospermum </i>on submerged rocks in clean running waters).','komárek (1992)',NULL,0,0),(797,117,'eco_distro','The single species grows aerophytic on insolated rocks in China.','komárek (1992)',NULL,0,0),(798,116,'eco_distro','Marine, in littoral on stones and shells. Occurs on limestone coasts in tropical and subtropical seas allover the world.','komárek(1992)',NULL,0,0),(799,120,'eco_distro','Epiphytic and epilithic species, growing in submerse, not polluted freshwater biotopes. Majority of species described from tropical countries and known usually only from few localities.','komárek (1992)',NULL,0,0),(800,118,'eco_distro','In the inner side of leaves of bromeliads and on environmental wooden substrates in a greenhouse of the Botanical Garden in São Paulo, Brazil. [type species]','fiore et al. (2007)',NULL,0,0),(801,119,'eco_distro','Only periphytic species, growing on water plants, other algae, on stones and wooden substrates in different aquatic habitats, particularly in not polluted biotopes. Several species are known from marine littorals (incl. the type species).','Komárek (1992)',NULL,0,0),(802,122,'eco_distro','Nine species are marine, occurring in littorals of different seas, mainly attached to other algae. Three freshwater species are known from the periphyton of algae and submerged plants in creeks and from littorals of pools and lakes from the northern temperate zone.','komárek (1992)',NULL,0,0),(803,115,'eco_distro','The type species grows subaerophytically on wet rocks and walls near Messina (Italy), but not known enough.','komárek(1989)',NULL,0,0),(804,123,'eco_distro','Only freshwater species growing sessile on aquatic<br> plants, on other algae and on stones, on which they cause sometimes coloured<br> (yellow, brown, blackish-violet) spots. One species is epizoic on planktic Crustaceans. <br> Many species have geographically limited areas of distribution; they are characteristic mainly for communities of periphytic algae in mountain creeks (the Alps, the Carpathians, etc.). However, the genus occurs all over the<br> world (different species in different frequences).','komárek (1992)',NULL,0,0),(805,125,'eco_distro','The single (type) species isolated repeatedly from garden soils and paddy fields in India (Uttar Pradesh, near Allahabad). Important model strains, used particularly for the study of atmospheric nitrogen fixation.','komárek (1992)',NULL,0,0),(806,126,'eco_distro','Known only from tropical countries (Africa, India, Indonesia); on wet rocks and epilithic submersely in clear springs and lakes.','komárek (1992)',NULL,0,0),(807,124,'eco_distro','Type species and two further species are known from sea littorals (epiphytic or epilithic), two species from hypersalinic lakes in central-asiatic USSR and in deserts of Egypt. Majority of species described from freshwater biotopes, usually from littoral and benthos of lakes and mountain creeks. <br> One species is aerophytic (growing on limestone-rocks; in caves and shaded places). Two species are known only from tropics, two species only from Antarctica.','komárek (1992)',NULL,0,0),(808,124,'eco_distro','Epilithic on limnestone rocks, described from Croatia (Yugoslavia), but not yet confirmed. Little known genus, the relation to Chlorogloea is particularly unclear.','komárek (1992)[sub lithocapsa]',NULL,0,0),(809,113,'eco_distro','Only in aquatic biotopes. Five species are known from the marine littoral or from salinic swamps, growing mainly periphytic on macroscopic algae or among organic detritus. Eight species grow in clear and usually cold springs and creeks (rarely also in stagnant waters) in mountains, mainly on mosses or submerse plants, rarely on stony substrates (usually in temperate zones in geographically distant localities); one species was described from a mountain creek in Portorico, few species are known only from central and SE-Asiatic high mountain regions, one species is known from streaming waters in Antarctica.','Komárek (1989)',NULL,0,0),(810,127,'eco_distro','Ecologically interesting genus: many species grow in different extreme biotopes, in periphyton of thermal and mineral springs, katharobic springs, alkalic or hypersalinic swamps, aerophytic or endolithic in stones in hot or Antarctic deserts, in polar regions, or symbiotic with lichens. Several species have cosmopolitan distribution, but they occur only in their special biotopes.','komárek (1992)',NULL,0,0),(811,128,'eco_distro','The type species was described from periphyton on water plants in one lake in Indonesia (Sumatra); not revised, no other known species.','komárek (1992)',NULL,0,0),(812,129,'eco_distro','Periphytic on stones in clear stagnant (lake littorals) and strea_ming water biotopes, usually in the mountain areas. Marine species not revised.','komárek (1992)',NULL,0,0),(813,131,'eco_distro','Yellowstone thermal waters (about 50 centigrades) with high iron content, pH &gt;7','Brown et al. (2005)',NULL,0,0),(814,130,'eco_distro','Widely distributed genus in freshwaters, less in salinic localities, mainly in metaphyton of waters of different kind, also in aerophytic, thermal and soil biotopes; a group of species lives in plankton of water reservoirs (few species facultatively with aerotopes). Many species were repeatedly incorrectly identified and misinterpreted (the ecology is important for the correct determination).','komárek (1992)',NULL,0,0),(815,132,'eco_distro','All species are known from clear, streaming or stagnant mountains waters,the commonest (and probably cosmopolitan) <i>C. setigerum</i> grows on algae and plants, <i>C. rivulare</i> usually on stones in European mountain areas; <i>C. sicyoideum</i> is known only from Chinese mountains. One species is known from Arctic Canadian lakes.','komárek (1992)',NULL,0,0),(816,133,'eco_distro','Both species are known from the metaphyton of swamps, one from freshwater (USSR, near Leningrad), the second one from salinic (USSR, Turkestan) localities.','komárek (1992)',NULL,0,0),(817,138,'eco_distro','The single species known still only from Yellowstone National Park, U.S.A. Terrestrial, atmophytic near thermal springs (places influenced by hot steam). A little known genus','komárek (1992)',NULL,0,0),(818,136,'eco_distro','Ten species are known from plankton of lakes and reservoirs across North America and worldwide (Prescott, 1962; Whitford and Schumacher, 1969; Duthie and Socha, 1976; Stein and Borden, 1979; Sheath and Steinman, 1982; some = <i>Woronichinia</i> spp.); they rarely occur in metaphyton (Komárek and&nbsp; Anagnostidis, 1998).','komárek (2003)',NULL,0,0),(819,136,'eco_distro','Well known species (<i>C. dubium</i>, <i>C. kuetzingianum</i> , <i>C. confertum</i>, <i>C. minutissimum</i>, etc.) are planktic, <i>C. dubium</i> is known only from northern Europe, three other probably with the cosmopolite distribution, the last two being more common in warmer and tropical areas. All species occur redominantly in large, not very eutrophicated reservoirs. The taxonomy, ecology and distribution of other species are still unclear.','komárek (1992)',NULL,0,0),(820,135,'eco_distro','Type species described from a lagoon on the island Laysan (Hawaii, USA), another one is not well described; the type species was not revised after the first description. Into this genus belongs possibly also <i>Coelosphaerium chlamydocystis</i> Skuja 1964.','komárek (1992)',NULL,0,0),(821,137,'eco_distro','Epiphytically on water plants or epilithic on stones in clear, unpolluted creeks, usually in mountains areas. Three species are described from Africa.','komárek (1992)',NULL,0,0),(822,140,'eco_distro','<a href=\"http//genome.jgi-psf.org/draft_microbes/crowa/crowa.home.html\">Link to genus page at JGI  Microbes</a><br>It occurs in ocean waters warmer than 24°C. It has been isolated from offshore open ocean oligotrophic waters in the western tropical Atlantic and from the tropical Pacific oceans where it may achieve cell densities exceeding 1,000 cells per milliliter within the euphotic zone. The size, abundance and rapid growth rate (i.e., 35 hour doubling time at 30°C) of <i>Crocosphaera</i> WH8501 indicate that this diazotrophic cyanobacterium is capable of contributing significantly to oceanic carbon and nitrogen budgets in the tropical regions of the world´s oceans.','From JGI Microbes',NULL,0,0),(823,142,'eco_distro','Planktic in stagnant freshwater, rarely (secondary) in running waters.','Rajaniemi et al. (2005)',NULL,0,0),(824,139,'eco_distro','The type species grows endogloeic in the mucilage of subaerophytic Aphanocapsa (on wet rocks in England), one species known from pools in Antarctica, another from soil biotopes in the Netherlands. One species from India is unclear.','komárek (1992)',NULL,0,0),(825,143,'eco_distro','The single (type) species is described and known only from one locality, from moist rocky substrate or mixed with other algae among mosses near the Jingbo Lake, Heilongjiang province, China.','komárek (1992)',NULL,0,0),(826,145,'eco_distro','The type strain was described from the culture. According to the ˝morphological as well as biochemical characters also other species belong to this genus, which grow in marine (saline) or freshwater phytoplankton (cf. picoplanktic species mentioned, e.g., by Y. Watanabe from Japan, G. Kennaway from Wales, Taylor et ale 1990 from England and Scottland, or red species presented by Ernst 1990 from Germany), in mucilage ot epiphytically of other, mainly planktic cyanophytes (known yet as different ˝small Synechococcus-like species˝; compo Chang 1980)) as well as several small periphytic or metaphytic Synechococcus- (e.g., <em>S. diatomicola</em>, <em>S. parvus</em>, etc.) or Cyanothece-species (without keritomic thylakoidal system, e.g., <em>C. gaarderi, C. cedrorum, C. eximia</em>, etc.).','Komárek (1992)',NULL,0,0),(827,144,'eco_distro','The type species was described from the culture, but further picoplanktic freshwater and marine species belong probably to this genus, which needs further study, particularly from the point of view of cytomorphology, life cycles, variation range of physiological and morphological characters, and ecology. The ˝Marine-cluster C of Synechococcus˝ with oceanic picoplanktic species (Platt et al. 1983, Waterbury 1989, Newman et Carr 1990, Waterbury et al.1979) belongs probably also to this genus.','komárek (1992)',NULL,0,0),(828,146,'eco_distro','Aerophytic species growing on almost nude calcareous soil in the lowland tropical area. Known only from the northern coast of Papua New Guinea (Madang province).','komárek (1992)',NULL,0,0),(829,147,'eco_distro','Planktic in eutrophic water bodies, known from the central Europe (Austria, Czechoslovakia, Germany). Very similar to some<br> <i>Cyanodictyon</i> species (cf. <i>Cyanodictyon imperfectum</i>).','komárek (1992)',NULL,0,0),(830,134,'eco_distro','All species prefer the stagnant freshwater biotopes (swamps, small´ - reservoirs). The type species is known only from North America (USA, Minnesota), two species from littorals of lakes and swamps in tropical countries (described from Cuba, from metaphyton among aquatic plants). C. pusillum is commonly spread in plankton of slightly eutrophized reservoirs in temperate and subtropic zones (probably cosmopolite), but occurring in several morphotypes.','komárek (1992)',NULL,0,0),(831,150,'eco_distro','All species live in aquatic biotopes, attached to different plants. Eight species (inclusive the type species) are freshwater (mountain creeks, not polluted streams, swamps, pools, tropical stagnant streaming waters), occurring mainly on aquatic mosses or on other algae, with different areas of distribution. The marine species occur attached to the littoral higher algae.','komárek (1992)',NULL,0,0),(832,155,'eco_distro','The type and single species, <i>C. venezuelae</i>, grows in metaphyton of periodical pools (salinic/freshwater ?) in old coastal corral areas, overgrown by vegetation, near tropical seas. Till now known only from the Caribbean district (Venezuela, Cuba).','komárek (1992)',NULL,0,0),(833,156,'eco_distro','In fresh or in slightly salinic waters, described from large lakes in Germany (Schleswig-Holstein) and in southern Sweden (Scania) and Finland, usually near the sea shore; probably widely distributed.','Komárek (1992)',NULL,0,0),(834,151,'eco_distro','The only species was described fromthe marine littoral of California (U.S.A.), where it grows epiphytically on the red alga of the genus Rhodymenia. This species destroys the surface cell layers of the host alga. A little known genus, its delimitation from Nematoradaisia is unclear.','komárek (1992, sub geitleriella)',NULL,0,0),(835,154,'eco_distro','Planktic in fishponds, ponds and small reservoirs (gravel pit lakes) in Central Europe (Austria, Czechoslovakia, Germany). Little known genus','komárek (1992)',NULL,0,0),(836,153,'eco_distro','Cyanodictyon species are mainly planktonic in oligotrophic to mesotrophic (rarely dystrophic) water bodies; one species is endgloeic within the mucilage of Anabaena (Geitler, 1932). Probably widely distributed.','Komárek (2003)',NULL,0,0),(837,153,'eco_distro','The type species lives endogloeic within mucilaginous colonies of planktic Anabaena species, the other species are free-living, planktic, in clear or eutrophized lakes, known mainly from northern Europe (Scandinavia, northern Germany) and northern N. America (Canada).','Komárek (1992)',NULL,0,0),(838,157,'eco_distro','Both species are known from periphyton; they grow attached to the filamentous algae, submersed plants and detritus particles, in more or less clear, unpolluted small water bodies, pools, backwaters, swamps, <i>C. mirabile</i> mainly in mountain areas of the whole temperate zone, <i>C. minor</i> in the central (Pannonian) basin of the river Danube (Europe).','komárek (1992)',NULL,0,0),(839,149,'eco_distro','Water bloom, thermal spring; Lake Bogoria, Kenya','Hindák (2002)',NULL,0,0),(840,158,'eco_distro','Marine. Boring into mollusc shells, rocks and other limestone substrates in water depths from 0.5 m above to 75 m below MWL, in ovoid grains from the shallow subtidal zone and in the intertidal zone. One species known from the shores of eastern Florida and Bermuda Islands, two from the limestone Mediterranean coasts of Greece.','komárek (1992)',NULL,0,0),(841,152,'eco_distro','Both species epilithic, described from stones in the littoral zone of lakes in Sumatra (Indonesia).','komárek (1992)',NULL,0,0),(842,159,'eco_distro','Several species growing in metaphyton and among detritus in stagnant or streaming, usually clear waters, sometimes with plenty of water plants, one species is known from moors, one is subaerophytic, three are known only from tropics, two were described from thermal springs. The type species is known from the periphyton of spring with cold (stenotherm) water.','komárek (1992)',NULL,0,0),(843,163,'eco_distro','The type species is freshwater, planktic, still known only from one eutrophic lake in S. Sweden (Scania).','komárek (1992)',NULL,0,0),(844,161,'eco_distro','The type species is described from the littoral of clear alpine lakes in the central Europe, two species are known from similar biotopes in China; one from Scandinavia, one species was described from plankton of the lake Volvi, Greece.','komárek (1992)',NULL,0,0),(845,167,'eco_distro','All cells described and known only from rocky limestone shores of Mediterranean Sea (Yugoslavia - Dalmatia, S. Greece).<br> Little known genus.','komárek (1992)',NULL,0,1),(846,166,'eco_distro','Mainly periphytic species, growing in benthos, on water plants and submersed woody and stony substrates, usually in not polluted and slightly eutrophized waters. Several species grow in soils. Mainly with geographically limited areas.','komárek (1992)',NULL,0,0),(847,162,'eco_distro','Not well known genus. In plankton and metaphyton of small, freshwater, not very eutrophicated and polluted water reservoirs, mainly with plenty of water plants, rarely in lakes. The type species is known from the central Europe, the other ones from the subtropical Cuba and from south Canadian lakes.','komárek (1992)',NULL,0,0),(848,169,'eco_distro','Little known genus, found only from a few localities. Four species are marine, living attached to the higher littoral algae, two species are freshwater, known from Sphagnum leaves in alpine moors (Switzerland) and from periphyton on algae in a clear lake in Chatham islands (type species).','komárek (1992)',NULL,0,0),(849,164,'eco_distro','In metaphyton of shallow pits, pools, moors, swamps and small lakes with plenty of water plants, rarely secondary in plankton; two (and probably more) species occur in salinic and hypersalinic swamps; few species grow subaerophytically on barks of trees wet rocks and in humid, several only in thermal spring.','komárek (1992)',NULL,0,0),(850,175,'eco_distro','Majority of species grows in water level or intertidal zones on rocky shores of seas allover the world and less of inland lakes, one species grows aerophytically on wet serpentine rocks in the central Europe.','komárek (1992)',NULL,0,0),(851,170,'eco_distro','The type species grows on submersed freshwater substrates. It was described from Italy (Sicily - wet and submersed rocks with streaming water) and later was found epilithic and epiphytic in littoral of lakes in Sweden. Ecological differences and both distant localities make genotype identity of both these populations uncertain.','komárek (1992)',NULL,0,0),(852,176,'eco_distro','Populations typically develop in benthic habitats (epipelic, among plants) in oligotrophic and mesotrophic pools, ponds, and lakes; sometimes they float in metaphyton or in plankton.','Komárek (2003)',NULL,0,0),(853,173,'eco_distro','The single species, <i>D. formosa</i>, has a special ecology: it was found only in streaming (waterfalls), very acid (pH = about 5.5) waters in Indonesia (Sumatra).','komárek (1992)',NULL,0,0),(854,174,'eco_distro','The up to now single species was described from a hypersalinic inland lake in central USSR (southern Siberia).','komárek (1992)',NULL,0,0),(855,177,'eco_distro','Marine, epilithic in the splash zone of calcareous coasts; known only from the Mediterranean region (Yugoslavia - Dalmatia). Little known genus.','komárek (1992)',NULL,0,0),(856,180,'eco_distro','Majority of species are subaerophytic, growing on wet (often acidic, peaty) soils, several species occur only in tropical forests (on bark of trees, mosses, etc.).','komárek (1992)',NULL,0,0),(857,181,'eco_distro','Tropical species, living submersely in clear water biotopes and subaerophytic on wet rocks.','komárek (1992)',NULL,0,0),(858,179,'eco_distro','The majority of species (5) is known from acidic and cold (stenotherm) swamps, peaty pools, raised bogs and clear lakes (mainly in temperate up to subpolar zones), inclusive the type species <i>E. alpina</i> ; one species is described from volcanic soils, one from slightly alkalic waters (swamps with water plants, channels, lakes, pools) of tropical and warmer areas of the temperate zone, two species are halophilic','komárek (1992)',NULL,0,0),(859,182,'eco_distro','Periphytic among other algae and water plants with plenty of detritus (tropical alkalic pools and swamps, moors in temperate zones, littoral of lakes), the type species is known from creeks and waterfalls in limestone mountains, one species was described from the littoral of tropical salinic lake. All species probably with geographically limited areas of distribution.','komárek (1992)',NULL,0,0),(860,184,'eco_distro','Aerophyiic, epilithic on calcareous rocks in caves. The type species is distributed probably worldwide (Israel, France, Roumania, Spain, Yugoslavia, USA, Cook Islands), but very distinct, only under very special ecological conditions (caves of a special- character, in deepest and least illuminated areas of the photic zone); the second species, G. floridana, grows under simi1ar conditions, but known only from the USA (Florida).','Komárek (1992)',NULL,0,0),(861,171,'eco_distro','The majority of species live periphytically on stones or on water plants in clear waterfalls, streaming water, on wet stony walls and in littorals of water reservoirs. Several species are known from marine littoral.','komárek (1992)',NULL,0,0),(862,171,'eco_distro','Plantae marinae vel aquae dulcis.','Bornet et Flahault (1886)',NULL,0,0),(863,185,'eco_distro','The both species grow attached to the water plants, filamentous algae, detritus particles and solid substrates in the littoral of clear or slightly eutrophized lakes, ponds and similarwater bodies. Known yet from the temperate zone of the Europe (Austria, Czechoslovakia, Finland, Germany).','komárek (1992)',NULL,0,0),(864,186,'eco_distro','Rarely growing in solitary filaments usually in mats, in soils or in submersed, not polluted freshwater biotopes, covering different substrates (leaves of plants, stones, wood, etc.). Several species are known from mineral or thermal springs.','komárek (1992)',NULL,0,1),(865,188,'eco_distro','Few species known from plankton of lakes and reservoirs and from metaphyton among water plants in swamps, usually in tropical regions (E. African lakes, Cuba, Ecuador, etc.). One species known from N. Europe, one from thermal springs in Yellowstone Park (USA).','komárek (1992)',NULL,0,0),(866,191,'eco_distro','The type species is marine (stony littoral in the surf zone), and-probab1y with world-wide distribution, other species grow subaerophytically on wet or periodically moistened rocks, walls and wooden substrates (known mostly from the temperate zone and high mountains of Eurasia), but probably more distributed. The subaerophytic mode of life causes the formation of different, morphologically variable modifications. Probably more species exist.','komárek (1992)',NULL,0,0),(867,189,'eco_distro','The single (type) species known from the culture, isolated from the surface of a limestone rock (Switzerland).','komárek (1992)',NULL,0,1),(868,193,'eco_distro','Two species are euplanktic, few species develop periphytically on water plants and on submerged stones and woods, but later sometimes liberate from the substrate and flow on the water surface. Several species live in the detritus (metaphyton) in swamps and reservoirs with abundant water vegetation. The majority of species have limited areas of distribution (tropic, nordic, etc.). All species are freshwater, only the planktic G. echinulata grows in both fresh and in brackish waters of<br> the temperate zone (e.g. in Baltic Sea).','komárek (1992)',NULL,0,0),(869,193,'eco_distro','Plantae aquae dulcis aut subsalsae.','Bornet et Flahault (1887)',NULL,0,0),(870,194,'eco_distro','The type species described from the drying pools on rocks in Romania. The validity of this genus was several times hesitated, because similar flattened and tube-like formation occur sometimes in different Oscillatoria-species as a drying effect (comp., e.g., Anagnostidis et Schwabe 1966). However, from the original type material exist several exsiccates (isotypes), which confirm the existence of this species. The genus was revised by Claus (1966), who described other species from<br> Hungary (aerophytic in caves, thermal springs); however, the genus needs in each case further investigations','komárek (1992)',NULL,0,0),(871,194,'eco_distro','Kleine, dünne Stäbchen, deren stumpfe Enden bogig zusammengekrümmt sind. Einzeln oder ganz vorübergehend zu zwei bis vieren zusammenhängend. Längsteilung.','Geitler (1932; sub <i>Cyanarcus</i>)',NULL,0,0),(872,195,'eco_distro','The majority of species free living in the methaphyton of the littoral of lakes and in swamps and pools, among other algae and water plants (one in salinic swamps), usually with limited areas of distribution. Three species are planktic in + clear lakes and ponds. Two species are exclusively tropical, the other are known predominantly from the temperate zone.','komárek (1992)',NULL,0,0),(873,192,'eco_distro','Majority of species is known from aerophytic localities, mainly from wet rocks in mountains, allover the world. Few species grow in metaphyton of clear small water bodies with plenty of detritus and water plants, one species was described from plankton of Scandinavian lakes.','komárek (1992)',NULL,0,1),(874,197,'eco_distro','Benthic cyanobacterial mats in heliothermal shallow hypersaline ponds along marine coast. [type species]','Margheri et al. (2008)',NULL,0,0),(875,190,'eco_distro','Majority of species is known from wet or dry, periodically moisted stony and rocky walls and from rocks with streaming water, distributed allover the world. The taxonomy of populations from different areas is not quite clear, but most species are considered as world-wide distributed. They occur mainly in mountains, but also in all other rocky areas, including the arid regions. Few species are periphytic and metaphytic in waters with water pmnts, very rarely occur in plankton and secondary in cryoseston in high mountains.','komárek (1992)',NULL,0,1),(876,200,'eco_distro','Majority of species are aerophytic, growing on stones and bark of trees, several species occur rarely in submerse biotopes. Distribution of various species is not well known, mainly because of many misidentifications.','komárek (1992)',NULL,0,1),(877,200,'eco_distro','Plantae terrestres.','Bornet et Flahault (1888)',NULL,0,1),(878,198,'eco_distro','Aerophytic, known only from dry walls in China (Yunnan).','komárek (1992)',NULL,0,0),(879,203,'eco_distro','All species are known from aquatic habitats, where they grow attached at different substrates (wood, stones, water plants, other algae, etc.). They occur in freshwater, as well as in marine biotopes. One species lives epizoic on planktic Crustaceans. The genus is known over the world, however, several species have limited areas of distribution or they are known only from few localities. Not yet in cultures.','komárek (1992)',NULL,0,0),(880,199,'eco_distro','Majority of species grow in stagnant waters (metaphytic, littoral of lakes, swamps), usually clear and with water plants (in tropical and temperate zones), several species prefer moors and peaty waters. One species occurs in thermal waters, two species grow subaerophytic.','komárek (1992)',NULL,0,0),(881,202,'eco_distro','Known from soils in Costa Rica. Probably nearly related to Chlorogloeopsis.','komárek (1992)',NULL,0,0),(882,204,'eco_distro','Epiphytic on the rhodophycean alga Sterrocladia, still known only from Guayana.','komárek (1992)',NULL,0,0),(883,201,'eco_distro','Both species are aerophytic, known from limestone rocks in Indonesia (species) and Papua-New Guinea.','komárek (1992)',NULL,0,0),(884,206,'eco_distro','Marine; all species described from Mediterranean Sea; they occur on rocky limestone shores, probably more distributed. The genus must by retypified and the generic name should be conserved in the sense of Ercegović (1930,1932) and, particularly, Le Campion et Golubić (1985).','Komárek (1998)',NULL,0,1),(885,205,'eco_distro','All species are known from submerse biotopes. The majority of species grow on stones (on the upper or bottom sides) or epiphytic in streams (particularly in mountain creeks), in tarns, less on different substrates in other stagnant waters. One species is marine, few live endogloeic within mucilage of other algae. Almost all species are known from geographically limited areas.','komárek (1992)',NULL,0,0),(886,209,'eco_distro','A little known genus containing periphytic species growing subaerophytically or in clear, freshwater submerse biotopes. Two species are known from China, one from Indonesia, one from Spain.','komárek (1992)',NULL,0,0),(887,208,'eco_distro','Both species are marine, growing on the muddy bottom of sea beaches or among marine algae. One species was described from Pacific islands, the second,one (type species) was recorded from Caribbean district, Canary Islands and from Mauritius.','komárek (1992)',NULL,0,0),(888,211,'eco_distro','Different species known from the periphyton in streaming, usually clear waters, or in lakes or marine littorals (growing on sand, stones or macroalgae). Two species with calcareous precipitations in sheaths (growing in waters in limestone areas). One species was described from periphyton on water plants in tropical swamps (Angola).','komárek (1992)',NULL,0,0),(889,211,'eco_distro','Plantae aquaticae, praecipue marinae.','Gomont (1892)',NULL,0,0),(890,210,'eco_distro','Type species known from stones, plants and wooden substrates in rapid floating, cold streams, mainly in mountains, probably with cosmopolitan distribution (however, this species is still little known and the identity of populations from different countries must be revised). Three other species (very little known, sometimes only from one locality) have similar ecology, one species was described from the littoral of lakes. Data of Hydrococcus from salinic waters and mineral lakes are uncertain.','komárek (1992)',NULL,0,0),(891,207,'eco_distro','Two species are known from marine localities (epi- or endozoic in everte- brates) , one species was isolated from soil in England.','komárek (1992)',NULL,0,1),(892,215,'eco_distro','Two species are marine, growing on stone surface and epiphytic on algae in shallow beaches (one cosmopolitan ?, one known from Japan), one species grows on wood and stones in the splash zone of littoral of clear streams in Finland.','komárek (1992)',NULL,0,0),(893,212,'eco_distro','The type species known from stagnant freshwater swamp,pools and ponds with vascular submerse plants (forming mats on water plants, rarely secondary floating). Recorded from several very distant areas (Europe, India, Japan, S. Argentine), but never well documented; the identity of all these records should be controlled.','komárek (1992)',NULL,0,1),(894,212,'eco_distro',' Both species are marine, growing on the muddy bottom of sea beaches or among marine algae. One species was described from Pacific islands, the second,one (type species) was recorded from Caribbean district, Canary Islands and from Mauritius.','Komárek (1992) sub <i>Hormothamnion</i>',NULL,0,1),(895,213,'eco_distro','All species grow in submerse biotopes, on limestone substrates, either in marine (stony and rocky sea littoral, shells,old corral reefs), or in freshwater biotopes (usually in not polluted creeks). Marine species probably with wide distribution in all seas of the tropical and temperate zones. In spite of it, majority of species is little known and needs further studies. Distribution of frehwater species is known a little only.','komárek (1992)',NULL,0,0),(896,216,'eco_distro','One species grows subaerophytic on wet walls, several are periphytic in different freshwater biotopes (springs, littorals of stagnant water), one species is planktic, one was described from soil.','komárek (1992)',NULL,0,0),(897,214,'eco_distro','Two species aerophytic and epiphytic, growing on bark and leaves of trees and on epiphytic mosses in tropical forests (Madagaskar, Antilles); one species grows on submerse wood in stagnant waters (Africa- Gaboon).','komárek (1992)',NULL,0,0),(898,217,'eco_distro','The type species lives submersely and epilithic in streaming water, known only from mountain creeks in India.','komárek (1992)',NULL,0,0),(899,218,'eco_distro','Mainly benthic organisms, growing on the bottom of diverse water biotopes, pools, lakes, reservoirs with rich vegetation of water plants, commonly in metaphyton. Several species known from mineral, thermal or salinic waters.','komárek (1992)',NULL,0,1),(900,219,'eco_distro','Several times was found and studied only the type species <i>J. pellucida</i>, which occurs in metaphyton of not polluted swamps, small water bodies with plenty of submersed vegetation and littorals of stagnant waters, all over the tropical regions and in warmer areas of the northern temperate zone. Other species have similar ecology, one species was described from thernal springs in Yellowstone Park (USA). Not yet well known genus, the revision in cultures is necessary.','komárek (1992)',NULL,0,0),(901,220,'eco_distro','Two species, described from oceanic plankton (Pacific) and one from Central European moors, correspond precisely to the generic diagnosis. Three others (clear freshwater reservoirs with water plants - Europe, and planktic in large water reservoirs in South Africa) grow in long filaments.','komárek (1992)',NULL,0,0),(902,222,'eco_distro','Marine; the single species grows on limestone rocks in the Mediterranean region (France, Greece, Yugoslavia).','komárek (1992)',NULL,0,1),(903,224,'eco_distro','The type species occurs rarely planktic in slightly eutrophized lakes in western Baltic region (southern Norway and Sweden, Denmark, northern Germany); two other species were described from small reservoirs with water plants in eastern Slovakia (Czechoslovakia), however, their generic position is not indisputable.','komárek (1992)',NULL,0,0),(904,221,'eco_distro','Mainly benthic species, living solitary or in fine mats on the sandy or muddy bottom of unpolluted lakes, pools, small water reservoirs and streams, in metaphyton on plants, rarely in plankton (particularly tychoplankton). Two species are known from thermal and mineral springs, one is endogloeic (grows in the mucilage of other planktic cyanophytes). Distribution not well known; different species have probably the limited ecological demands and areas of distribution.','komárek (1992)',NULL,0,0),(905,223,'eco_distro','Majority of species grow epiphytic on other filamentous and thallic algae and water plants. Both freshwater and marine species are known. A little known genus, not yet in cultures.','komárek (1992)',NULL,0,0),(906,225,'eco_distro','<i>Leptolyngbya</i> species are very common in soils and in periphyton and metaphyton of freshwater and halophilous (marine) biotopes, several species are known from thermal and mineral springs or from aerophytic rocky sites or walls; characteristic species grow endogloeic in<br> mucilage and in colonial slime of other algae. They grow well in cultures and are available for cultivation, one strain of ˝<i>Plectonema boryanum</i>˝ (=<i>Leptolyngbya boryanum</i>) was used as a model strain for bioassays. Taxonomy is not well known in respect of their morphological simplicity.','komárek (1992)',NULL,0,1),(907,227,'eco_distro','Sessile, epilithic and on shells of molluscs in streaming waters in tropical countries (equatorial Africa).','komárek (1992)',NULL,0,0),(908,165,'eco_distro','All <i>Cylindrospermopsis</i> species are known from plankton of freshwater eutrophic reservoirs in tropical, subtropical or temperate regions (in summer), where they form sometimes water-blooms. In tropics, the appearance is often connected with nitrogen limitation ofphytoplankton. With increasing data about distribution and importance appeared a necessity of detailed autecological studies of <i>C. raciborskii</i>. We select several important ecological articles for information: Baxter (1996), Bormans (1999), Dokulil &amp; Mayer (1996),<br> Fabbro &amp; Duivenvoorden (1996), Padisák (1991, 1999, 2002), Présing &amp; al.(1996), Komárková &amp; al. (1999), Gorzó (1987), Vörös (1995). - As a water-bloom forming species, <i>Cylindrospermopsis</i> (particularly <i>C. raciborskii</i>)<br> belongs to important dominant cyanobacterial plankters of eutrophic reservoirs in all tropical regions, and recently also in temperate zone. Majority of populations produce cyanotoxins (cylindrospermopsin),<br> which insert this genus among the most important cyanobacterial types in the present water management. Already wide literature exists about toxicity of <i>Cylindrospermopsis</i>(see special papers); we list here only the basic titles (in an alphabetic order): Baker (1996), Carmichael &amp; al. (2001), Chiswell &amp; al. (1999), Chorus &amp; Bartam(1999), Eaglesham &amp; al. (1999), Falconer (1996), Falconer &amp; al. (1999), Francis (1878), Hawkins &amp; al. (1985), Lagos &amp; al. (1997, 1999), McGregor &amp; Everding (1998), Ohtani &amp; al. (1992), Seawright &amp; al. (1999), Saker &amp; Eaglesham (1999), Schembri &amp; al. (2001), Senogles &amp; al. (2000), Shaw &amp; al. (1999, 2000), Skulberg &amp; al. (1993), Thomas &amp; al. (1998), Vörös (1995) and many others.','Komárek (2002: 35)','',0,0),(909,165,'eco_distro','All species planktic in eutrophized water basins (water blooms), commonly in tropical countries; more common <i>A. raciborskii</i> facultatively also in temperate zones during the summer seasons.','komárek (1992)',NULL,0,0),(910,230,'eco_distro','The single species L. ramosus was described as endolithic, subaerophytic cyanophyte from localities in calcareous rocky areas in Croatia (Yugoslavia) and not yet revised or proved from other regions.','komárek (1992)',NULL,0,0),(911,232,'eco_distro','The single (type-) species grows epiphytically, submersely on water plants and algae, mainly is reported from freshwater Batrachospermum. Known only from Brasil. Maybe only a stage of Nostochopsis.','komárek (1992)',NULL,0,0),(912,228,'eco_distro','Mainly as a symbiont in colonial ascidians. [type species]','myiashita et al. (2003)',NULL,0,1),(913,229,'eco_distro','Planktic or tychoplanktic species,<br> occurring in freshwater, mesotrophic up to eutrophic reservoirs (lakes,<br> ponds, artificial valley reservoirs). The most common type species (L. redekei)<br> is distributed all over the temperate zones, the founds from tropical countries<br> must be revised. The distribution of different species is not quite clear<br> because of many misidentifications by authors. More known are species from<br> temperate zone.','komárek (1992)',NULL,0,1),(914,233,'eco_distro','Grows aerophytic, described from wet human bones in Melanesia and found also on limestone substrate in Papua New Guinea. The data from a polluted river near Berlin (central Europe) are very probably incorrect.','komárek (1992)',NULL,0,0),(915,231,'eco_distro','The single (type) species grows in clear creeks-in North America, where it forms several cm thick, layered mats, which take substantial part in travertine production. In spite of this, it was not yet confirmed; the generic identity with Aphanothece is possible.','Komárek (1992)',NULL,0,1),(916,238,'eco_distro','Both species are freshwater, growing attached to the stony substrate in streaming waters; tropical species (India, Tunisia).','komárek (1992)',NULL,0,0),(917,234,'eco_distro','Usually growing in mats covering different subaerophytic or submerse substrates, several species are marine or brackish. Rarely occur in clusters of tangled filaments in metaphyton of not very polluted water bodies with_numerous water plants. Few species occur in plankton as solitary trichomes (rarely -L. birgei, etc.). Common all over the world (mainly the halophilic species).','komárek (1992)',NULL,0,0),(918,234,'eco_distro','Plantae aquae salsae, dulcis aut thermalis, nunquam terrestres.','Gomont (1892)',NULL,0,0),(919,235,'eco_distro','The single species known only from the warm creeks with stony beds in Great Antilles (Cuba, Portorico).','komárek (1992)',NULL,0,0),(920,239,'eco_distro','The type species, <i>M. laminosus</i>, is typical obligatory thermophilic species and occurs in thermal springs throughout the world (including Antarctica). However, it is very probably dependent on a special set of environmental conditions (temp. 45-60°C, pH &gt;7.5, aerobic, low salinity), and all other records, particularly from cold water belong evidently to other species. Also the very wide variability, ascribed to M. laminosus, concern probably in some cases a mixture of genotypic different procaryotes. Other species must be revised.','komárek (1992)',NULL,0,0),(921,237,'eco_distro','Type species described from periphyton on filamentous algae in sea littorals; to this genus belong probably further cyanophytes, which grow attached to similar substrates and which were described as different Xenococcus species (but not reproducing by nanocytes and growing only in spherical cells; e.g. <i>X. gracilis, X. minimus</i>, <i>X. schousboei</i> p.p., etc.).','komárek (1992)',NULL,0,0),(922,240,'eco_distro','The aerophytic type species was described from bark of trees in New Kaledonia and not recorded again.','komárek (1992)',NULL,0,0),(923,242,'eco_distro','Marine; the single species was described from shells of molluscs (Petunculus) on the coast of Sicily, Italy.','komárek (1992)',NULL,0,0),(924,243,'eco_distro','Free floating in water or in metaphyton, detritus, among water plants, usually in submerged biotopes with numerous water vegetation. Several small species are planktic, several live in halophilic biotopes (sea shores, salinic swamps) or in thermal springs. Distribution allover the world, but several species have clearly ecologically and geographically limited areas of distribution. To this genus belongs evidently also ˝Low GC-cluster of Synechocystis˝, defined by Waterbury (1989; freshwater, with facultative gliding motility, forming flat sheets, photoautotroph, facultatively containing phycoerythrins in cells).','komárek (1992)',NULL,0,0),(925,241,'eco_distro','Marine; creeping epili thic on calcareous stones and on the surface of shells of molluscs, distributed over the European, South African and American coasts of temperated and subtropical zone. Data from freshwaters (M. testarum var.aquae-dulcis from rivers in Russia) should be revised.','komárek (1992)',NULL,0,0),(926,244,'eco_distro','Majority of species grow epiphytic on algae and submerse plants in moors, swamps and ponds, few species are epilithic in streaming water or in littoral of lakes. Few species are known from algae in marine littoral, several taxa occur only in geographically limited areas (tropical regions). One strain used as an important experimental model organismus under the name ˝Fremyella diplosiphon˝(probably able to chromatic adaptation).','komárek (1992)',NULL,0,0),(927,245,'eco_distro','Mainly benthic and soil species, covering the substrate or growing in psammon under a slight layer of wet sand. Several species known from sandy and muddy marine beaches and river aestuaries or from other types of sea coasts or inland salinic biotopes. Several species are known from wet soil or from littoral of clear or slightly polluted water bodies, where they cover mud or water plants. Known also from wet rocks and mineral springs.','komárek (1992)',NULL,0,0),(928,245,'eco_distro','Plantae terrestres aut aquaticae, nonnunquam marinae.','gomont 1892',NULL,0,0),(929,246,'eco_distro','Epipelic and metaphytic species growing mainly in small water bodies (pools and waters with water vegetation or with sandy substrate), but two species are known from brackish up to salinic localities in flat sea beaches and in riverine aestuaries (M. sabulicola, M. marina). Known from northern temperate zone, rarely from tropics (mainly not revised data).','komárek (1992)',NULL,0,0),(930,247,'eco_distro','Free floating in plankton of freshwater, more or less eutrophic water reservoirs (sometimes forming heavy water blooms). Several species live benthic in moors, epiphytic or epilithic in different types of stagnant and running waters and on wet rocks. Many species have world wide distribution (with exception of subpolar regions), but several taxa are ecologically and therefore also fytogeographically limited. The majority of not-planktic species without ability to form gas vesicles belongs probably to the genus <i>Aphanocapsa</i>.','komárek (1992)',NULL,0,0),(931,248,'eco_distro','Subaerophytic in sandy desert soil.','Řeháková et al. (2007)',NULL,0,1),(932,249,'eco_distro','Cell division transverse, perpendicular to the longitudinal axis, in the same plane in successive generations, into two, more or less isomorphic daughter cells soon separating from one another (rarely asymmetrically).','komárek & anagnostidis (1998)',NULL,0,0),(933,249,'eco_distro','Little known and sporadically occurring genus. The type species was described from brackish waters in Philippines, one species grows planktic in hypersaline lakes (Near East), one free floating in pools in southern Africa (Angola). Probably more species described under other generic names, usually from tropical regions and more or less extreme (hypersalinic) biotopes.','komárek (1992)',NULL,0,1),(934,252,'eco_distro','The single species was described from creeks in the central Sumatra (Indonesia), where it grows on the surface of stones.','komárek (1992)',NULL,0,0),(935,251,'eco_distro','In metaphyton and periphyton in submerse habitats among algae and water plants, in hot and mineral springs; majority of species occurs in aerophytic biotopes (wet rocks, tree trunks), including the type species. About distribution is little known, but many species have probably the limited areas of distribution in respect of the special ecology.','komárek (1992)',NULL,0,0),(936,253,'eco_distro','The single (type) species grows aerophytically among other algae on the bark of trees in mountains (1140 m), so far known only from China (the upper river Xin-pen). From wet rocks in Asian mountains are known populations representing probably further species of this genus.','komárek (1992)',NULL,0,0),(937,254,'eco_distro','Four defined species (including the type species <i>N. spumigena</i>) are planktic with aerotopes within the cells forming sometimes heavy water blooms. They occur rarely in freshwater reservoirs, mainly in slightly salinic or brackish waters, salinic and coastal lakes (Baltic Sea; aestuaries of rivers - Spain, Australia; lakes in Western coast of North America, etc.). Three species are benthic, always without aerotopes, occurring in coastal or inland salinic and mineral pools, marshes and lakes (<i>N. harveyana</i>) , in alkalic streams and in littoral of lakes and pools (<i>N. sphaerocarpa</i>) or in rice fields as an important fixator of nitrogen (<i>N. willei</i>). <i>N. harveyana</i> has probably cosmopolitan distribution, <i>N. sphaerocarpa</i> is known mainly from the temperate zone (Europe), <i>N. willei</i> is probably pantropic. From other little known species, one is described from Antarctica, few taxa live surely in soils (probably special species), one species was described from thermal waters.','komárek (1992)',NULL,0,0),(938,250,'eco_distro','Marine, growing endophytically in marine red and brown algae. Probably more widely distributed, but still little known.','komárek (1992)',NULL,0,0),(939,256,'eco_distro','Freshwater; all species grow attached (old colonies later sometimes free floating) to mosses, atones and submersed wood in not polluted creeks and streams, known over the whole tropical zone (one variable species or several taxa ?). Rarely found also in temperate zone, sometimes from stagnant pools (different species ?).','Komárek (1992)',NULL,0,0),(940,255,'eco_distro','Different species grow in freshwater biotopes, epipelic, epilithic and epiphytic in not polluted lakes, ponds and pools, many species grow in different soils (especially from the subgenus Amorphonostoc) or on their surface. N. flagelliforme from Chinese semi deserts is edible. Several species are important components of subpolar soil or water-biotopes and nitrogen-fixers. Few species grow endophytically in fungi, (Geosiphon), mosses, liverworts, ferns and vascular plants (roots of Cycas, Gunnera). In world collections are numerous isolated strains, which are, however, insufficiently identified.','komárek (1992)',NULL,0,0),(941,257,'eco_distro','The type species grows periphytic (epiphytic on other algae and cyanophytes) in warm and thermal springs in tropical countries (Indonesia - Java, Zambia).','komárek (1992)',NULL,0,0),(942,261,'eco_distro','The only species described from stony, ferric littoral of one lake in Sweden. Very little known genus, not revised after the first description. From the genera Chlorogloea or Chondrocystis differs only by the ferric precipitations.','komárek (1992)',NULL,0,0),(943,258,'eco_distro','All species grow in mats on different substrates (mud, stones, sandy bottom, etc.), mainly in shallow water biotopes, in littoral regions of freshwater reservoirs and seas, in pools, rarely on wet soils. Characteristic are the ˝floating Oscillatorieta˝, developing primarily benthic, later floating as macroscopic clusters on the water surface (sometimes in masses). Distribution allover the world, but several species have the geographically limited areas of distribution.','Komárek (1992)',NULL,0,0),(944,258,'eco_distro','Plantae hydrophilae, thermales vel halophilae, raro et casu terram humidam incolenles.','Gomont (1892)',NULL,0,0),(945,260,'eco_distro','Free-floating (planktic) in lakes, small reservoirs, sometimes in slightly salinic water. One species originally attached to filamentous algae or submersed plants, secondary living meristonic.','komárek (1992)',NULL,0,0),(946,263,'eco_distro','Isolated from soils (including paddy fields), known only from tropical areas (India, Egypt). Very near to Westiellopsis.','komárek (1992)',NULL,0,0),(947,262,'eco_distro','Marine; creeping on the gelatinous membranous outgrowth of Strombus-shell. Known only from the littoral of Xisha Islands, South China Sea.','komárek (1992)',NULL,0,0),(948,264,'eco_distro','Both species distinguish in dimensions and slightly in cell form, and grow epiphytically on leaves on Sphagnum, or Potamogeton; described from Czechoslovakia (Bohemia). Not found after description, very problematical genus with strange morphology in cyanophytes (revision is needed; according to Drouet et Daily 1956 = fungi).','komárek (1992)',NULL,0,0),(949,265,'eco_distro','Subaerophytic or submersely (freshwater), epilithic, on soil or epiphytic, several species are known from geographically limited areas (tropical species).','komárek (1992)',NULL,0,0),(950,259,'eco_distro','Both species were described from one locality, wetted wood and calcareous stones in a limestone cave, Hungary (Abaliget). Mixed among other algae.','komárek (1992)',NULL,0,0),(951,269,'eco_distro','in plankton of eutrophic gravel pit lakes. Type locality: gravel pit lake Štrkovec in Bratislava, W Slovakia','Hindák (2002)',NULL,0,0),(952,268,'eco_distro','Three species known from rocky littorals of seas and oceans; freshwater species described from wet rocks with streaming water or from streams of different kind from very distant localities allover the world. Little known genus, which needs further studies.','Komárek (1992)',NULL,0,0),(953,267,'eco_distro','Rarely solitary filaments, usually in mats on different aeric or water substrates (soil, wet rocks, mud, water plants, stones and woods in both stagnant and streaming waters), some species occur in the marine littoral. Several species are known from extreme lacalities (thermal springs, desert soils, etc.), few of them take part in the biolithogenic processes and form travertine crusts in limestone water biotopes.','komárek (1992)',NULL,0,0),(954,267,'eco_distro','Plantae terrestres vel aquaticae, haud frequenter halophilae.','gomont (1892)',NULL,0,0),(955,272,'eco_distro','Almost all species are planktic, few of them causing the water blooms, mainly in mesotroph or slightly eutrophised up to eutrophic reservoirs (usually lakes). One species (Pl. cryptovaginata) grows in metaphyton of unpolluted pools and ponds among submerse water plants. Two species have cosmopolite distribution, another ones are geographically limited, mainly occurring under special ecological situations; two species are known from tropical countries only.','Komárek (1992)',NULL,0,0),(956,270,'eco_distro','Planktic species, usually in large, mesotrophic reservoirs; several species are limited only in tropical and warm areas of temperated zones, several species are presumably nordic.','komárek (1992)',NULL,0,0),(957,275,'eco_distro','Both species described from the surf zone of the calcareous rocky littoral of mediterranean coast in Dalmatia (Yugoslavia). Little known genus, which needs revision.','komárek (1992)',NULL,0,0),(958,273,'eco_distro','In clear (usually katharobic to oligosaprobic) water basins, springs or creeks, in metaphyton and periphyton.','komárek (1992)',NULL,0,0),(959,274,'eco_distro','Type species and several other taxa known from the sea littorals (surf- or intertidal zones); freshwater species known usually from clear mounta,in streams or from the stony surf zones of not polluted lakes and water reservoirs, all over the world. Majority of species grow on limestone substrates.','Komárek (1992)',NULL,0,0),(960,277,'eco_distro','Mainly aerophytic and subaerophytic algae occurring on wet rocks (often in mountains), rarely on barks of trees, on the mud and in soil. Few species are described from marine littoral, several are known from periphyton in clear submerse localities.','komárek (1992)',NULL,0,0),(961,279,'eco_distro','It has so far only been found, perhaps as a facultative symbiont, associated with didemnid ascidians in marine litoral habitat.','Lewin (1976)',NULL,0,0),(962,279,'eco_distro','It has only been found growing epizoically on calcified colonial ascidians (<i>Didemnum</i> spp.) in subtropical coastal waters.','Lewin (1975)',NULL,0,0),(963,281,'eco_distro','The single species was described from filaments of Porphyrosiphon in Angola, and not found and revised again.','komárek (1992)',NULL,0,0),(964,282,'eco_distro','Several species live planktic, tychoplanktic or benthic in oligotrophic, mesotrophic up to slightly eutrophic water reservoirs, other species grow in soil or endogloeic in colonial planktic rotifers or in mucilage of other algae. Few species are known from extreme biotopes (mineral and hot springs, salinic or hypersalinic localities).','komárek (1992)',NULL,0,0),(965,284,'eco_distro','The type species described from the stony littoral zone of the lake Bodensee (Switzerland/Germany). Very little known and not revised genus, possibly a stage of an bangiacean species (Rhodophyceae).','komárek (1992)',NULL,0,0),(966,285,'eco_distro','Periphytic species, known from soils, different submerse substrates (mainly stones), one species known from streams with intensely flowing water, another species lives endogloeic within mucilage of other algae.','komárek (1992)',NULL,0,0),(967,287,'eco_distro','The epiphytic type-species was described from water mosses (Fontinalis) in-littoral of one lake in Sweden.','komárek (1992)',NULL,0,0),(968,288,'eco_distro','Majority of species known from marine biotopes, one species described from streams in central Africa. All species need taxonomic revision; they are very little known, not found again after their description.','komárek (1992)',NULL,0,0),(969,283,'eco_distro','From the four described species, one is known from the subaerophytic localities in calcareous rocks (Europe), one from tropical soils, one from halophilic swamps and one from the plankton of Caspian sea. Probably more species distributed, but overlooked or misinterpreted with other cyanophytes (Chroococcus, Myxosarcina, Gloeocapsa, etc.).','komárek (1992)',NULL,0,0),(970,286,'eco_distro','The type species was described from the ˝dirty pond˝ in Malaysia, 4 species are known from pools, wet rocks and waterfalls in high mountains (Alps, Carpathians, Himalaya), 1 species was isolated from soils in Aroentine.','komárek (1992)',NULL,0,0),(971,289,'eco_distro','The type species occurs commonly in plankton of the nordic lakes in the Europe, northern Japan and North America, where occurs in the typical form. This species is published often also from other regions, especially of the temperate zone, but also from tropical countries. The genotypic identity of such populations with the type species should be proved.','komárek (1992)',NULL,0,0),(972,294,'eco_distro','Grows epilithic on stones in creeks with streaming water, usually in forest zone, in shaded places; type species described from the Austrian Alps and not yet revised. The second species (unclear) is known only from streams in mountain areas in England.','komárek (1992)',NULL,0,0),(973,295,'eco_distro','Marine, endophytic within cells (intracellular) or rarely epiphytic (on the surface of frustules) of oceanic, planktic Diatoms (Rhizosolenia, Hemiaulus, Chaetoceros, etc.), mainly in warm, tropical seas.','komárek (1992)',NULL,0,0),(974,292,'eco_distro','Several planktic species, few taxa were described from metaphyton and detritus in not polluted water biotopes with numerous water plants. One species is kryosestonic, one is known from salinic water.','Komárek (1992)',NULL,0,0),(975,296,'eco_distro','Only periphytic species, often on calcareous substrates (and then intensely incrusted by calcium carbonate), but exist also epilithic and epiphytic, not incrusted species. Important members of travertine-forming biocenoses. Several species known from marine littoral; in fresh waters, they prefer clear, unpolluted, streaming or stagnant waters.','Komárek (1992)',NULL,0,0),(976,296,'eco_distro','Plantae marinae, subsalsae, rarius aquae dulcis.','Bornet et Flahault (1886)',NULL,0,0),(977,293,'eco_distro','Ten to fifteen species are known, mostly planktonic in lakes and reservoirs, but also endogloeic in Microcystis colonies (Komarek and Anagnostidis, 1998). One metaphytic species occurs in acidic peaty swamps.','komárek (2003)',NULL,0,0),(978,293,'eco_distro','Majority species planktic (usually in large lakes) or living in metaphyton of clear water bodies, one species known only from tropics. One species is kryosestonic from spring and summer snow fields.','komárek (1992)',NULL,0,0),(979,297,'eco_distro','* freshwater plankton and metaphyton (12)<br> -mass developments (2 cases: S. Bohemia, Brazil - Caruaru)<br> * marine plankton (1)<br> * cryoseston (2) __<br> * benthic - epipelic (2)<br> * benthic -&gt;-metaphytic - mountain streams (1)<br> * aerophytic (on mosses) (1)<br>','komárek, sulek et hauer(2003)',NULL,0,1),(980,297,'eco_distro','Mainly planktic species, usually from large, clear up to mesotrophic or slightly eutrophic reservoirs, lakes and ponds, rarely (<i>R. simplex</i>) from the hypertrophic pond; one species is known from marine plankton (Mexico Gulf), where it grows sometimes joined by one end to detritus particles. Majority of freshwater planktic species known only from northern temperate zone.','komárek (1992)',NULL,0,0),(981,297,'eco_distro','Einzelne Arten sind planktische Organismen, die in Seen, Teichen und Flüssen vorkommen. Eine Art hat man aus dem Benthos dänischer Seen beschrieben, wurde jedoch bisher noch nicht bestätigt. Alle Arten sind bisher nur aus Europa bekannt, nur Kol beschrieb <i>R. elegans</i><br> var. <i>nivicola</i> aus dem Kryoseston im Yellowstoner Nationalpark in den USA','Komárek (1958: 160)',NULL,0,1),(982,297,'eco_distro','Forma planctonica, habitat lacus ad Leopolim in Polonia.','Koczwara (1929: 108, sub <i>Raciborskia</i>)',NULL,0,1),(983,298,'eco_distro','surface seawater [type species]','Choi et al. (2008)',NULL,0,0),(984,299,'eco_distro','All unsufficiently described species from communities of subaerophytic localities, wet rocky walls and stony littoral of lakes.','komárek (1992)',NULL,0,0),(985,300,'eco_distro','Many species grow in littoral of lakes joined to the stony or wooden substrates (usually in surf zone) or in metaphyton among water plants and in moors and swamps. Characteristical are the Inactis-species, forming crusty hemispherical colonies or layers on stones and rocks in littoral zone of lakes, streaming water or on wet rocks, usually in limestone areas. Several species are known from sea coasts and salty biotopes, other live in springs, mineral and thermal springs or in waterfalls. Aerophytic species grow also in wet soils, often in moors. Several representants of the subg. Symplocastrum form characteristical mats with erected Symploca-like fascicles<br> on wet, not polluted forest soils or old wooden substrates. The species from the section <i>Hypheothrix</i> (Kutzing) Lemmermann belong probably to the genus <i>Phormidium</i>.','komárek (1992)',NULL,0,0),(986,300,'eco_distro','Plantae terrestres vel aquaticae, nunquam omnino marinae, frequenter in stillicidiis vigentes.','gomont (1892)',NULL,0,1),(987,301,'eco_distro','Tropical aerophytic and freshwater species. The type species is known from humid, subaerophytic biotopes (epiphytic on liverworts, tree-trunks, on humid walls, etc.) in India, two other species are known from swamps in Antilles (alkaline swamps in Cuba; Guadeloupe).','komárek (1992)',NULL,0,0),(988,302,'eco_distro','Many Scytonema-species grow aerophytic or subaerophytic on wet rocks, wood, soil, epiphytic on mosses; several species are incrusted by calcium carbonate and represent dominant members of microphytes in travertine springs. Few species are known from atmophytic habitats near thermal waters. The submersely living species grow usually in rocky littoral of lakes, rarely among water plants, mainly on alkalic substrate, rarely in moors or acidic waters, few species are marine, occurring on corral reefs or in brackish water. The genus is very common mainly in tropical regions, but particularly the variability of tropical taxa is unsufficiently known and many species are arbitrarily misinterpreted.','komárek (1992)',NULL,0,0),(989,303,'eco_distro','Periphytic and metaphytic species, five species´ are known from tropical re- gions (rice fields, littoral of lakes, springs, swamps), one species is ma- rine, one described from thermal springs (USA), one from the rocky littoral of lakes and submersed stones of the alpine zone of Central European high mountains.','komárek (1992)',NULL,0,0),(990,306,'eco_distro','The type species S. polonicum grows epilithic in the surf zone of cold and clear mountain (alpine) streams and littorals of lakes; till now known from the limestone areas of the European high mountain areas (Alps, highest part of Carpathians, etc.). Second species described from thermal springs in Czechoslovakia (western Carpathians).','komárek (1992)',NULL,0,0),(991,308,'eco_distro','Mainly periphytic species, growing (four species), other species known from thermal and mineral springs.','komárek (1992)',NULL,0,0),(992,308,'eco_distro','Plantae marinae.','gomont (1892)',NULL,0,0),(993,310,'eco_distro','The single (type) species grows epizootically on legs of a Hydracarine Neumania triangularis. Described from the central Asia, from the central Asia, from the vicinity of Buchara, and not revised.<br> According to Geitler (1942), it is possibly a Trichobacterium.','komárek (1992)',NULL,0,0),(994,304,'eco_distro','Aerophytic and atmophytic species, described from wet walls and mosses, from the nature and glasshouses; known from Italy and Austria.','komárek (1992)',NULL,0,0),(995,305,'eco_distro','The type species was isolated from soil in Romania.','komárek (1992)',NULL,0,0),(996,311,'eco_distro','Marine. On limestone shores in tide and surf zones. Described from the Mediterranean Sea (Dalmatia, Yugoslavia), but more distributed.','komárek (1992)',NULL,0,0),(997,307,'eco_distro','The type species was described from the plankton of the lake Balaton (H, SE Europe), and not confirmed yet from other localities.','komárek (1992)',NULL,0,0),(998,309,'eco_distro','Seven species are known from the plankton of temperate fresh and brackish waters, particularly from cold, northern, mesotrophic lakes (Komarek and Anagnostidis, 1998).','Komárek (2003)',NULL,0,0),(999,309,'eco_distro','Cell division only by binary fission in two planes in successive generations, perpendicular to one another and to the colony surface; disintegration of colonies even into solitary cells.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(1000,309,'eco_distro','Freshwater (or in slight brackish biotopes), mainy in plankton of large, slightly eutrophized reservoirs, rarely secondary in metaphyton. Several species are known only from limited areas (1 from<br> North-American large lakes, 2 from northern regions of N temperated zone, 1 from Alpine lakes), two species possess probably +/- world-wide distribution (S. litoralis, S. lacustris).','Komárek (1992)',NULL,0,1),(1001,313,'eco_distro','Planktonic in eutrophic water bodies','Azevedo et Sant\'Anna (2003)',NULL,0,0),(1002,312,'eco_distro','Three species were described from aerophytic localities, wet rocks and walls in limestone areas in Southern Italy. All other species and localities should be revised.','komárek (1992)',NULL,0,0),(1003,316,'eco_distro','Several species are benthic or grow in metaphyton of freshwater biotopes, usually in not heavy artificially polluted waters, in detritus among water plants. Several species prefer thermal and mineral springs, ˝Sulphuretum˝ - communities, or halophilic biotopes (marine coastal and brackish waters).','komárek (1992)',NULL,0,0),(1004,316,'eco_distro','Plantae hydrophilae vel halophilae, in stratum continuum agglomerata aut inter varias Algas sparsa.','Gomont (1892)',NULL,0,0),(1005,317,'eco_distro','Two species are known from the periphyton of alkalic lakes and swamps in Cuba and in Austria (Nesider lake), one species is known from the marine littoral.','Komárek (1992)',NULL,0,0),(1006,319,'eco_distro','On stones in springs, creeks, rarely in lake littoral. Tropical species, known from equatorial Africa and Indonesia.','komárek (1992)',NULL,0,0),(1007,318,'eco_distro','The type species was isolated from the soil sample collected from cavities in granitic rocks near the ancient city Zimbabwe, Zimbabwe.','komárek (1992)',NULL,0,0),(1008,315,'eco_distro','Arid soils, Utah, Texas, USA','flechtner et al.(2002)',NULL,0,0),(1009,322,'eco_distro','Aerophytic species, described from wet calcareous rocks in south China (Kwangsi).','komárek (1992)',NULL,0,0),(1010,321,'eco_distro','Stigonema-species occur in various biotopes allover the world, usually attached to the substrate or in soil, but not very common. More in tropical regions. Many species grow aerophytically or subaerophytically on bark of trees or wet rocks, from lowland to the alpine zone of high mountains (different species). Several species are known from pools, swamps and moors, where they grow in metaphyton or attached to stones and wood. Important are soil species in tropical habitats.','komárek (1992)',NULL,0,0),(1011,290,'eco_distro','Only planktic, freshwater species, sometimes forming slight water blooms, several species occur only in geographically limited areas (tropical species, China, etc.).','komárek (1992)',NULL,0,0),(1012,320,'eco_distro','Majority of species was described from different tropical regions, where they grow epiphytically on other algae and submerged water plants. The most common type species, S. sansibaricus, has pantropical distribution, but it was found also in basins with thermal water and tropical water plants in temperate zone. One species is known from Himalayas, another one grows on stones in Alpine creeks in the European high mountain areas.','komárek (1992)',NULL,0,0),(1013,329,'eco_distro','The type species-described from volcanic rocks near thermal springs (atmophytic) in the island Pantellaria, Italy, the other species are known from calcareous substrate of thermal springs in Yellowstone National Park, USA and from thermal waters in Japan.','komárek (1992)',NULL,0,0),(1014,327,'eco_distro','Several species are planktic in fresh water reservoirs or in salinic or sea waters, other grow in metaphyton of pools, of thermal and mineral springs, of salinic (brackish) swamps or in moors. The ˝Marine cluster of Synechocystis˝, defined by Waterbury (1989), belongs evidently to this genus. The ˝Aphanocapsa˝ species found within hollow hairs of polar bears in zoos (comp. Lewin 1979) is evidently also a Synechocystis species.','komárek (1992)',NULL,0,0),(1015,323,'eco_distro','The type species was described from the culture, isolated from paddy-field soil in India (Katni).','komárek (1992)',NULL,0,0),(1016,326,'eco_distro','Several species grow within mats and colonies of other algae, or form fine colonies on wet substrates (mud, wood, stones, etc.). A group of species is known from the metaphyton and periphyton of thermal and mineral springs few are described from aerophytic sites. Interesting picoplanctic or planktic species were found in oceans as well as in freswater reservoirs (lakes) (S. rhodobactron and others). The genus is surely heterogeneous and its taxonomy must be solved by help of ultrastructural procedures and by methods of molecular taxonomy. The “Marine cluster A” (with motile cells, reddish cell content, with chromatic adaptation,<br> photoautotroph; comp. Waterbury 1989) represents evidently a special, botanically not yet revised genus.','komárek (1992)',NULL,0,0),(1017,324,'eco_distro','Majority of species are aerophytes growing on wet soil, rocks, walls or wet mosses. Several species are marine, known from stony littorals of seas, three species were described from the edges of thermal springs, influenced by hot water steam (atmophytic).','komárek (1992)',NULL,0,0),(1018,324,'eco_distro','Plantae terrestres aut hydrophilae, rarius halophilae.','gomont (1892)',NULL,0,1),(1019,330,'eco_distro','thermophilic','Katoh et al. (2001)',NULL,0,0),(1020,331,'eco_distro','The type species was found in a very polluted stream of organic nature (effluent of a creamery), attached to the stony substrate, in the Vaal River, southern Transvaal, South Africa. Never revised, further observations are necessary.','komárek (1992)',NULL,0,0),(1021,332,'eco_distro','Mainly submerse, growing in littorals of not polluted water reservoirs on stones or among other algae and water plants, in springs, mineral springs, streams, pools, etc.; several species are ecologically limited (they grow only in moors, alkalic swamps, in limestone areas, etc.). Many species are known_only from tropical biotopes, however, they need mostly taxonomic revisions. Several species are described from aerophytic habitats (wet sandy soils, bark of trees, wet stones, calcareous or sandstone walls, etc.).','komárek (1992)',NULL,0,0),(1022,335,'eco_distro','Majority of species live in soil (incl. the type-species), less are periphytic in littorals of different waters (important are species from rice fields, which are intense nitrogen fixators); few species are known from marine littorals. A couple of ecologically interesting species grow endophytically in intercellular spaces of <i>Azolla </i>or in roots of several Cycadaceae. Many species are known only from tropics, only few are distributed in temperate or subpolar zones.','komárek (1992)',NULL,0,0),(1023,339,'eco_distro','The type species was isolated from plankton of a lake in central Japan (the planktic populations with dominant not branched trichomes can be misinterpreted with Raphidiopsis). The type culture TAC 101 is kept in Japanese algal strain collections. Umezakia is the single planktic member of Stigonematales.','komárek (1992)',NULL,0,0),(1024,334,'eco_distro','Only planktic species, from which three are freshwater (rarely occurring in large water reservoirs), the other are marine. They cause sometimes reddish water blooms in tropical seas and oceans, sometimes in lower layers (several meters under the water level).','komárek (1992)',NULL,0,0),(1025,334,'eco_distro','Plantae sociales, pelagicae, innumerabili copia per aequora calidiora vagantes.','Gomont (1892)',NULL,0,0),(1026,342,'eco_distro','The type species isolated from garden soil samples, India (Madras).','Komárek (1992)',NULL,0,0),(1027,338,'eco_distro','Planktic, tychoplanktic or benthic species, known mainly from North-European, oligotrophic, mesotrophic or slightly eutrophic water reservoirs. Probably mainly cold-stenotherm species, distributed in colder parts of temperate zone.','komárek (1992)',NULL,0,0),(1028,337,'eco_distro','Soil species (type-species) known up to now only from the vicinity of St. Peterburg (USSR).','komárek (1992)',NULL,0,0),(1029,340,'eco_distro','Described from wet limestone rocks (attached to the substrate) in Croatia and not revised again. The data from Czechoslovakia are uncertain.','komárek (1992)',NULL,0,0),(1030,341,'eco_distro','One species is atmophytic, growing near thermal springs in volcanic areas of South Italy (island Pantelleria), second species described from tropical soils.','komárek (1992)',NULL,0,0),(1031,345,'eco_distro','Little known genus, the type species described from freshwater swamps in South Africa, the second one is marine, both not yet revised.','komárek (1992)',NULL,0,0),(1032,347,'eco_distro','Attached to different substrates (stones, algae, water plants) in different water biotopes; several species are known from mountain streams, other ones from the sea littorals. Several species have<br> probably the special areas of distribution. A little known genus.','komárek (1992)',NULL,0,0),(1033,344,'eco_distro','Freshwater species; the type-species is known from several localities (stagnant waters) in North America (firstly joined to the substrate, later free floating). The second species (<i>W. bharadwajae</i>) was described from pond and paddy field bottom in India.','komárek (1992)',NULL,0,0),(1034,348,'eco_distro','Attached to different substrates, usually epiphytic. All species known still now only from streaming mountain waters.','komárek (1994)',NULL,0,0),(1035,349,'eco_distro','The type species is known from calcareous rocks (not or rarely perforating the substrate) in the upper littoral belt in Adriatic Sea and southern Japan.','Komárek (1992)',NULL,0,0),(1036,346,'eco_distro','Almost all species are planktic or tychoplanktic,less metaphytic or epipelic, few are known only from limited areas in the Europe (Scandinavian lakes, clear swamps in central Europe, etc.), from North America or from Himalayas. Three species with obligatory possessing aerotopes cause occasional ˝water blooms˝ in eutrophized reservoirs, two in temperate zones, one in tropics.','komárek (1992)',NULL,0,0),(1037,118,'eco_distro','Known from greenhouse of the Botanical Garden in São Paulo, Brazil. [type species]','fiore et al. (2007)',NULL,0,0),(1038,197,'eco_distro','Guerrero Negro, Baja California Sur, Mexico. [type species]','Margheri et al. (2008)',NULL,0,0),(1039,165,'eco_distro','Cylindrospermopsis is primarily a tropical genus. The type species, ˝Anabaena˝(=<i>Cylindrospermopsis</i>) <i>raciborskii</i>, was found and described in 1912 from Indonesia (Java), and this species was later recorded under various names from almost all tropical regions, from India (Bruhl &amp; Biswas 1922, Desikachary 1959, Singh 1962, Hortobagyi 1969, Seenayya &amp; Subba Raju 1972), Philippines (Taylor 1932, Behre 1956: fa. <i>maior</i> and fa. <i>minor</i>), Egypt (Brunnthaler 1914), Japan (Negoro 1953), Brazil ( Cronberg 1978, Branco &amp; Senna 1991, Sant´Anna 1991, Bouvy&amp; al. 2000), Cuba (Komárek 1984), Australia (Hawkins &amp; al. 1985, Baker &amp; Fabbro 1995), etc. Recently, numerous data exist about heavy water blooms of the pantropical <i>Cylindrospermopsis raciborskii</i> from the whole tropical Asia, Africa, Australia, central and South America and from numerous Oceanic Islands. Moreover, the 7 new common <i>Cylindrospermopsis</i> species described in the period of 1990-2003, almost all spread in different areas of tropical regions, prove the diversification ability and ecological potential of this genus. Another indication of development and vitality of <i>Cylindrospermopsis</i> is the invasive pressure of <i>C. raciborskii</i> into temperate zones, and the formation of different morphotypes in different parts of its wide geographic area. Already Kogan (1956), Obuchova &amp; Kosenko (1964) and Proškina-Lavrenko &amp; Makarova (1968) described several species from central Asia (Turkmenistan, Kazakhstan, Caspic Sea), which all belong to the vicinity of <i>C. raciborskii</i>, but their stability and relations are unclear (Fig. 2). In 1955, Prescott &amp; Andrews described one probably <i>Cylindrospermopsis</i> species from Kansas (Wooster Lake) in North America (<i>Anabaenopsis seriata</i>). Later, since the studies of Hill (1970, from Minnesotta lakes), several north American localities of <i>Cylindrospermopsis</i> are known, particularly from southern states of USA and Mexico. The first European record of <i>C. raciborskii</i> (sub <i>Anabaenopsis</i>) was published probably by Skuja (1937) from the lake Kastoria in Greece (Tab. 6B). In 1942, Szalai registered the first population of <i>Cylindrospermopsis</i> from Hungary {<i>Anabaenopsis raciborskii</i> var. <i>longiscellula</i>; Fig. 2H). Further populations from Pannonian district were registered by Hamar (1977), Jeeji Bai &amp; al. (1977), Schmidt (1977), Horecká &amp; Komárek (1979), Padisák (1991,1997) and others.<i> C. raciborskii</i> forms now common regular populations in the lowland of Danube river. Kondrateva (1968) recorded localities from southern Ukraine (Odessa district, basin of Danube river) and Aksenova (1974) from the river Don. Further records are known from lakes in Danube delta (Kaštovský, orig. data). The species collected also from Slovakia and Moravian part of the Czech Republic by Hindák (1988), and from Austria by Claus (1961; ˝<i>Anabaenopsis woloszynskae</i>˝; Fig. 2G), Dokulil &amp; Mayer (1996), and Dokulil &amp; Teubner (2000). In 2002 there were reported localities also from Germany (Nixdorf and Mischke, pers. comm.). The next European localities are known from Italy (Ventura pers. comm.), and from central and southern France (Coute &amp; al. 1997, 2003) (Fig. 5).','komárek & komárková (2003)',NULL,0,0),(1040,165,'eco_distro','Invasion of <i>C. raciborskii </i>in Europe. Main selected records.','Komárek &amp; Komárková (2003)','[177]',0,0),(1041,165,'eco_distro','All species occur in tropical regions and several of them form rich populations, dominating in phytoplankton community in tropical reservoirs. Up to know, only one species (type-species, <i>C. raciborskii</i>) is well known and studied, evidently from two reasons: this pantropical species has tendency to invade warm regions of temperate zones (in Europe, it is well known from Mediterranean countries, south France, Pannonian region), where it forms also water blooms. The second reason of its study is the intense production of cyanotoxins (cylindrospermopsin).','Komárek (2002: 35)',NULL,0,0),(1042,228,'eco_distro','The shallow waters of the Republic of Palau, probably widely<br> distributed in the tropical and subtropical marine coastal environment.<br> Growth characteristics. Heterotrophic growth in the light or dark was not observed even in various. [type species]','myiashita et al. (2003)',NULL,0,1),(1043,248,'eco_distro','Known from Cadiz Valley, Joshua Tree National Park, San Bernadino County, California, USA.','Řeháková et al. (2007)',NULL,0,1),(1044,279,'eco_distro','Known from Mangrove swamps in Baja California, Mexico.','Lewin (1975)',NULL,0,0),(1045,298,'eco_distro','Known from Chuuk lagoon, Micronesia [type species]','Choi et al. (2008)',NULL,0,0),(1046,308,'diagnosis','<b>Diagnosis of Dasygloea</b><br>\r\nVaginae amplissimae, hyalinae aut luteo-fuscae. trichomata. intra vaginam paucissima, valde remota. Apex trichomatis rectus, haud capitatus. ','Thwaites, [in English Botany, tab. 2941, 1848. - Kutzing, Species Algar., p. 272] ex <u>Gomont 1892</u>',NULL,0,0),(1047,255,'other','<em><strong>Nostoc</strong></em> is a genus of cyanobacteria found in various environments that forms <a href=\'https://en.wikipedia.org/wiki/Colony_(biology)\' title=\'Colony (biology)\'>colonies</a> composed of <a href=\'https://en.wikipedia.org/wiki/Filamentation\' title=\'Filamentation\'>filaments</a> of <a href=\'https://en.wiktionary.org/wiki/moniliform\' title=\'wiktionary:moniliform\'>moniliform</a> cells in a gelatinous sheath.<br>The name <em>Nostoc</em> was coined by <a href=\'https://en.wikipedia.org/wiki/Paracelsus\' title=\'Paracelsus\'>Paracelsus</a>.<sup><a href=\'https://en.wikipedia.org/wiki/Nostoc#cite_note-1\'>[1]</a></sup><br><em>Nostoc</em> can be found in <a href=\'https://en.wikipedia.org/wiki/Soil\' title=\'Soil\'>soil</a>, &nbsp;on moist rocks, at the bottom of lakes and springs (both fresh- and &nbsp;saltwater), and rarely in marine habitats. It may also grow <a href=\'https://en.wikipedia.org/wiki/Symbiosis\' title=\'Symbiosis\'>symbiotically</a> within the <a href=\'https://en.wikipedia.org/wiki/Tissue_(biology)\' title=\'Tissue (biology)\'>tissues</a> of <a href=\'https://en.wikipedia.org/wiki/Plant\' title=\'Plant\'>plants</a>, such as the evolutionarily ancient angiosperm <em><a href=\'https://en.wikipedia.org/wiki/Gunnera\' title=\'Gunnera\'>Gunnera</a></em><sup><a href=\'https://en.wikipedia.org/wiki/Nostoc#cite_note-2\'>[2]</a></sup> and the <a href=\'https://en.wikipedia.org/wiki/Hornwort\' title=\'Hornwort\'>hornworts</a> (a group of <a href=\'https://en.wikipedia.org/wiki/Bryophyte\' title=\'Bryophyte\'>bryophytes</a>), providing <a href=\'https://en.wikipedia.org/wiki/Nitrogen\' title=\'Nitrogen\'>nitrogen</a> to its host through the action of terminally differentiated cells known as <a href=\'https://en.wikipedia.org/wiki/Heterocysts\' title=\'Heterocysts\'>heterocysts</a>. These bacteria contain photosynthetic pigments in their cytoplasm to perform <a href=\'https://en.wikipedia.org/wiki/Photosynthesis\' title=\'Photosynthesis\'>photosynthesis</a>.','Wikipedia, the free encyclopedia',NULL,0,0),(1048,102,'other','<em><strong>Anabaena</strong></em> is a <a href=\'https://en.wikipedia.org/wiki/Genus\' title=\'Genus\'>genus</a> of <a href=\'https://en.wikipedia.org/wiki/Filamentation\' title=\'Filamentation\'>filamentous</a>\r\n<a href=\'https://en.wikipedia.org/wiki/Cyanobacteria\' title=\'Cyanobacteria\'>cyanobacteria</a> that exist as <a href=\'https://en.wikipedia.org/wiki/Plankton\' title=\'Plankton\'>plankton</a>. They are known for <a href=\'https://en.wikipedia.org/wiki/Nitrogen-fixing\' title=\'Nitrogen-fixing\'>nitrogen-fixing</a> abilities, and they form <a href=\'https://en.wikipedia.org/wiki/Symbiosis\' title=\'Symbiosis\'>symbiotic</a> relationships with certain plants, such as the <a href=\'https://en.wikipedia.org/wiki/Mosquito_fern\' title=\'Mosquito fern\'>mosquito fern</a>. They are one of four genera of cyanobacteria that produce <a href=\'https://en.wikipedia.org/wiki/Neurotoxin\' title=\'Neurotoxin\'>neurotoxins</a>, &nbsp;which are harmful to local wildlife, as well as farm animals and pets. &nbsp;Production of these neurotoxins is assumed to be an input into its &nbsp;symbiotic relationships, protecting the plant from <a href=\'https://en.wikipedia.org/wiki/Grazing\' title=\'Grazing\'>grazing</a> pressure.<br>A <a href=\'https://en.wikipedia.org/wiki/DNA\' title=\'DNA\'>DNA</a>\r\n<a href=\'https://en.wikipedia.org/wiki/Sequencing\' title=\'Sequencing\'>sequencing</a> project was undertaken in 1999, which mapped the complete <a href=\'https://en.wikipedia.org/wiki/Genome\' title=\'Genome\'>genome</a> of <em>Anabaena</em>, which is 7.2 million base pairs long. The study focused on <a href=\'https://en.wikipedia.org/wiki/Heterocyst\' title=\'Heterocyst\'>heterocysts</a>, which convert <a href=\'https://en.wikipedia.org/wiki/Nitrogen\' title=\'Nitrogen\'>nitrogen</a> into <a href=\'https://en.wikipedia.org/wiki/Ammonia\' title=\'Ammonia\'>ammonia</a>. Certain species of <em>Anabaena</em> have been used on <a href=\'https://en.wikipedia.org/wiki/Rice\' title=\'Rice\'>rice</a>\r\n<a href=\'https://en.wikipedia.org/wiki/Paddy_field\' title=\'Paddy field\'>paddy fields</a>, proving to be an effective natural <a href=\'https://en.wikipedia.org/wiki/Fertilizer\' title=\'Fertilizer\'>fertilizer</a>.','Wikipedia, the free encyclopedia',NULL,0,0),(1049,374,'other','Lorem ipsum dolor sit amet, ei per corpora reprimique, per ne nominati mediocrem. Ne tollit placerat qui, admodum reprimique ea qui, ne eam stet inani feugait. Eos adhuc aliquam recteque cu. Eam tractatos theophrastus in. Ne mel nisl voluptatibus, sit viris legimus ad.<br>Ex quidam repudiandae nec, at debet virtute electram mei. Soluta postea habemus et pri. Nam in ferri definiebas. Eu tractatos necessitatibus vim, ut sed nisl melius adolescens.<br>Quod adipisci complectitur cu vel, ex amet impetus fabulas quo, ea eos molestiae efficiendi. Delenit gloriatur adolescens ne has, qui at oblique consequat. Ad eos agam postulant. Porro temporibus dissentiet has at, sea no luptatum convenire consequuntur, ea laudem omnesque verterem mei. Has molestie contentiones ei, in hinc wisi ius, pri quidam accumsan ex. Magna invenire perpetua eu quo, an fuisset disputando vim. Dolor hendrerit mel ex, nec in aliquid consetetur, nec volumus lucilius consequuntur no.<br>Splendide consetetur nec ex, mei tamquam saperet accusamus ad, vix ridens eligendi liberavisse ne. Et usu nonumy iudicabit, virtute recteque periculis pro ei. Quot porro dolorem ut usu, eu duo quando legendos. Ut case dictas vel. Mei primis persecuti complectitur ei.<br>Ad eos enim imperdiet aliquando, in sit aeque solet disputando. Sint adolescens te has, in ius platonem iudicabit. Eu nulla saepe admodum nam, partiendo consequuntur mei an. Fugit movet dolores no est, ad sea erant eloquentiam. Clita labore has ea, oratio alterum vix no, et nec suas justo nonumes.','<u><strong>Lorem Ipsum</strong></u>','[415]',0,0),(1050,297,'diagnosis','Cellulae plus minus inclinatae, nunquam rectae, 3.7 — 8.3 X 0.6 — 0.8 um, aequaliter crassae, apicibus rotundatae, materiam pallide coeruleam homogeneam continentes, indumento ex muco hyalino, latitudine cellularum aequaliter crasso singillatim circumdatae, et per ipsum inter se conglutinatae, sine muco communi, plerumque pro ratione paucae in coloniis sphaeroideis, raro singillatim dispositae; per divisionem multiplicantur.','<span data-field=\'content\' data-froala=\'intermediate\' data-harvest=\'froala\' placeholder=\'Type something\'>Hortobagyi et Hilliard (1965: 141) [diagnosis of <em>Campylotropium</em>]:</span>',NULL,0,0),(1051,383,'other','Tralalalá','blabla',NULL,0,1),(1052,383,'other','zxczxczx','cacxcczxczxczxc',NULL,0,1),(1053,374,'eco_distro','It lives.','Me',NULL,0,0),(1054,448,'etymology','The species is named after the Atlantic Rainforest, where the species was first found.','Hentschke et al. 2017',NULL,0,0),(1055,447,'etymology','Genus named in honor of Professor Jiří Komárek','Hentschke et al. 2017',NULL,0,0),(1056,453,'description','Colonies multicellular, micro- to macroscopic (up to several centimeters &nbsp;in diameter), with cells arranged irregularly, loosely or densely in &nbsp;common mucilage, gelatinous, spherical or (usually) amorphous, greenish, blue-green or brown. Common mucilage fine, colourless, homogeneous and &nbsp;diffluent (subg. <em>Anathece</em>), or distinct, delimited, more or less smooth on the surface, structureless (subg. <em>Cyanogastrum</em>), &nbsp;or in marginal parts lamellate and yellowish or yellow- brown (rarely &nbsp;reddish), with cells in their own indistinct or distinct and/or &nbsp;lamellose, delimited envelopes (subg. Aphanothece). Cells widely oval to &nbsp;cylindrical (rod-shaped) with rounded ends, rarely oval-fusiform, &nbsp;straight or slightly arcuate, sometimes with clearly visible chromatoplasma; in a few planktic species solitary aerotopes occur &nbsp;facultatively.','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1057,603,'description','True branching heterocytous genus found distributed as dried mats. Shows close resemblance to species of <em>Westiellopsis </em>but lacks coccoid masses in main filaments along with lacking hormocytes in the branches. Prominently T-type branched. Main reason for its separation is a unique and strong phylogenetic position based on the 16S rRNA gene.','Kabirnataj et al. 2018',NULL,0,0),(1058,408,'description','Colonies free-living, usually in metaphyton or rarely on soil, cubic, &nbsp;with cells, arranged three-dimensionally in perpendicular rows; &nbsp;sometimes large colonies composed of sub- colonies; colonies small, &nbsp;few-celled or ,multicellular with up to more than 128 cells; rows mold &nbsp;colonies sometimes a little disturbed. Mucilage colourless, hyaline, &nbsp;delimited, rarely diffluent (sometimes almost invisible); special &nbsp;gelatinous envelopes around cells are absent or indistinct, facultative. &nbsp;Cells spherical or widely oval before division.','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1059,408,'reproduction','Cells divide regularly in three perpendicular planes in successive &nbsp;generations without displacement of daughter cells (this type of &nbsp;division causes development of regular cubic colonies); cells grow into &nbsp;the original spherical form before next division. Reproduction by colony &nbsp;disintegration.','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(1060,190,'reproduction','<span data-field=\'note\' data-froala=\'intermediate\' data-harvest=\'froala\'>Various &nbsp;Gloeocapsa species grow in morphologically very diverse stages, &nbsp;independence on seasonal and local environmental changes. The various &nbsp;status (st. ˝familiaris˝, ˝simplex˝, ˝lamellosus˝, ˝coloratus˝, &nbsp;˝perdurans˝, etc.) were described in numerous species. The knowledge of &nbsp;seasonal variability of the whole population is therefore necessary to &nbsp;the correct identification.</span>','Komárek (1992)',NULL,0,0),(1061,606,'description','Cells cyanoprokaryotic, solitary or in irregular clusters, sometimes pseudofilaments, oval or cylindrical, cell content homogenous, parietal thylakoids. Color of cells is blue-green. Reproduction by binary fission.','Dvořák et al. (2014)',NULL,0,0),(1062,189,'description','Cells solitary or aggregated in irregular groups, widely oval or rod &nbsp;shaped, surrounded by narrow, delimited gelatinous envelopes, containing &nbsp;one or more ensheathed cells. Cells non motile. Cell division by simple binary transverse fission, perpendicular to the long axis of the cell. Reproduction probably by liberation of solitary ensheathed cells or small groups of cells.<u><br></u>','Komárek &amp; Anagnostidis (1998)',NULL,0,0),(1063,593,'description','Widely spread genus with members comprising strains from rice fields of Thailand, water bodies of India and saline-alkaline lakes of Brazil. All members show close morphological resemblance to the genus Nostoc with almost nodistinguishable differences being evident. A promising diacritical feature is the presence of motile hormogonia with gas vesicles. The filaments are loosely arranged with variable tendencies for coiling. The ecology of this genus is diverse, and it is possible to assign a specific habitat for most of the Aliinostoc strains. The water resources from where the organisms are isolated are rich in total dissolved ions, salts etc., as revealed from high water conductivity. Another striking feature is that more new species belonging to this genus could be anticipated from both southern and northern latitudes on both sides of the Equator indicating a possible pattern of biogeographical distribution centering around the tropical regions.','Bagchi et al. (2017)',NULL,0,0),(1064,595,'description','Thallus caespitose, forming extensive mats, brown to green. Filaments straight, (8.1-) 9.5–15.7 µm diam. Sheath hyaline, thin or thick, ﬁrm, sometimes lamellated. Trichomes green to light-brown, occasionally slightly constricted at the cross-walls, (6.9-) 7.9–12.8 µm diam. Short cells, 1.3–2.1 µm long, 5.0–6.0 times larger than long. Cell content green, usually granulated, with numerous gas vesicles. Cross-walls granulated, with large granules. Apical cells rounded or conical-rounded, sometimes capitate, rare thickened. Hormogonia formed by straight fragmentation helped by necridic cells, or often in diagonal position, in this case helped or not by necridic cells.','Caires et al. 2018',NULL,0,0),(1065,581,'diagnosis','Filamentous cyanobacteria, forming bright green compact biofilms on aerophytic substrata or dark green mats on submerged substrata. Sheaths very thin, rare, colourless, 4.5–7.0 µm wide. Trichomes cylindrical, uniseriate, not or slightly constricted at the cross-walls, attenuated and bent at the ends. Cells cylindrical, shorter than wide to isodiametric, without aerotopes. Cell content slightly granular, blue–green. Apical cells conical-rounded and narrowed, calyptra absent. Thylakoids radially distributed in the cells; in the lateral view, organized in bundles situated irregularly over the whole protoplast. All cells are capable of division. Reproduction by fragmentation of trichomes by necridic cells. Heterocytes and akinetes missing.','Martins et al. (2016)',NULL,0,0),(1066,611,'description','Trichomes solitary, cylindrical, up to 3.5 um wide, constricted at the cross walls. Sheaths absent. Cells cylindrical, longer than wide. Terminal cells rounded. Thylakoids arranged radially. Akinetes and heterocytes not observed.','Nguyen et al. (2013)',NULL,0,0),(1067,400,'description','Unicellular rods with oxygenic photoautotrophic metabolism and gliding motility. Contain chlorophyll a and phycocyanin and photosynthetic thylakoids located peripherally. Reproduction by transverse binary fission in a single plane. Do not produce well-defined sheath layers. Contain spherical inclusions of earth alkaline carbonates in the cytoplasm.','Moreira et al. (2017)',NULL,0,0),(1068,614,'description','Exhibits the following properties in addition to those given in the genus description. Cells are 1.1 μm wide and 3.9 μm long on average. Growth occurs at 15–30 C (optimum 25 C) in alkaline freshwater and BG11 medium. The G+C content of the genomic DNA of the type strain is 52.2 mol%.','Moreira et al. (2017)',NULL,0,0),(1069,615,'description','Macroscopic colonies in nature hemispherical to spherical to irregularly globular, with tapering trichomes &nbsp;embedded in the colonial mucilage but extending outside of the mucilage to impart a fuzzy appearance to the colony. Filaments with distinct lamellated sheath, which is often funnel- or collar-like at the distal ends. Trichomes typically largest at the base and tapering to a thin hair distally, arranged in parallel, singly, or doubly false branched, sometimes forming concentric layers in large colonies. Heterocytes basal or rarely intercalary. Akinetes absent, but large swollen arthrospores present in some species.','Shalygin et al. (2017)',NULL,0,0),(1070,618,'diagnosis','Thallus solitary or forming small colonies, composed from heteropolar filaments, falsely branched and fan-like divaricated. Filaments composed from one trichome in a colorless or slightly brownish, thin sheath. Trichomes cylindrical, slightly and continually narrowed toward ends, terminal cells rounded. Cells more or less isodiametric or slightly shorter or longer than wide. Heterocytes solitary or in twos, basal or intercalar, akinetes or arthrospores are missing. Reproduction by hormogonia and fragmentation.','Komárek et al. (2015)',NULL,0,0),(1071,630,'description','Long flexuous and curved filaments, red-brown in colour. Trichomes, often false branched, slightly constricted at the cross wall, surrounded by a multilayered colorless sheath. Cells from isodiametric to longer than wide, 1.1-4.4 μm long and 1.2-2.1 μm wide, with parietal thylakoids. Apical cells rounded or tapered. Reproduction by fragmentation of trichomes in short hormogonia, without necridic cells.','Sciuto et al. (2017)',NULL,0,0),(1072,658,'other','BBB 333','Blabla',NULL,0,0),(1073,658,'other','bbb 444','blublu',NULL,0,0),(1074,658,'other','bbb 444 222','blibli',NULL,0,0),(1075,1101,'description','Comparison of the reference strain’s appearance with the original publications is shown on Fig. 1. Trichomes blue-green, highly motile, not constricted at the cross-walls, narrowing toward the often bent ends, 24–36 μm wide in the central area of the trichome and 14–27 (30) μm wide at the ends. Apical cells nearly hemispherical and often yellowish (together with up to five adjacent cells). Granulation never located at the cross-walls, but fine to larger granules randomly dispersed throughout cells. Cells 2–9 μm long, new cell walls form from the outside of the trichome often before the previous division is finished. Cell wall colourless and thick, necridic cells present, no sheath or calyptra observed.','Mühlsteinová et al. 2018',NULL,0,0),(1076,1101,'eco_distro','Blue-green mats first probably growing on the bottom of fresh-water reservoirs, later often released and floating at the water surface.','Mühlsteinová et al. 2018',NULL,0,0),(1077,258,'description','','Mühlsteinová et al. 2018',NULL,0,1),(1078,258,'description','Trichomes bluegreen to brownish-green, occasionally purple when old, highly motile, not or slightly constricted at the cross-walls, sometimes narrowing toward the often bent ends, central section of trichomes (19) 22–80 μm wide. Apical cells rounded and sometimes yellowish (together with several adjacent cells). Granulation never located at the cross-walls, but fine to large granules may be present in the cells. Cells much shorter than wide, new cell walls forming perpendicularly to the trichome axis, often before the previous division is finished. Cell wall colourless and thick, necridic cells present, sheath observed only in culture under stress conditions. No calyptra observed.','Mühlsteinová et al. 2018',NULL,0,0),(1079,1108,'description','Trichomes isopolar, cylindrical, regularly spirally coiled with a tendency to loosening the coils, unbranched, more or less tapering towards the ends, not or slightly constricted at cross-walls, blue green or dark green. Cells always shorter than wide. Terminal cells rounded or subcapitate with thickened outer cell wall or calyptra.','Nowicka-Krawczyk et al. 2019',NULL,0,0),(1080,1108,'eco_distro','Planktic in freshwater as well as in water with higher salinity, most of the species known so far prefer habitats with elevated pH and electrical conductivity.','Nowicka-Krawczyk et al. 2019',NULL,0,0),(1081,1125,'description','Thallus blue-green. Filaments straight, curved, or entangled, without branching. Trichomes uniseriate, cylindrical. Sheaths thin, colorless, fibrous monolayer. Cells longer than wide, cylindrical, distinctly constricted at the cross wall, not attenuated at the ends. Apical cells rounded.','Zhou et al. 2018',NULL,0,0),(1082,1126,'description','Thallus blue-green. Filaments straight or coiled, uniseriate, without false branching, 1.75–2.28 μm wide. Sheath thin, colorless, attached to trichomes. Trichomes cylindrical, distinctly constricted at the cross wall. Cells longer than wide, 2.23–3.46 μm long and 1.04–1.73 μm wide. Apical cells rounded, sometimes extended, without calyptra, longer than wide, 1.86–3.66 μm long and 1.24–1.85 μm wide. Thylakoids parietal, varying from three to four at the lateral portion. No heterocytes. Gas vesicles absent. Cyanophycin granules (CG) and lipid droplet (ld) present.','Zhou et al. 2018',NULL,0,0),(1083,1126,'eco_distro','pH 8.09; Conductivity 40.79 ms/ccm; dissolved oxygen 103.8% sat; salinity 26.4‰','Zhou et al. 2018',NULL,0,0),(1084,1127,'description','Thallus blue-green. Filaments straight or curved to floating mats, without branching. Sheath thick, multilayer, covered the trichomes. Cells cylindrical and elongated, distinctly constricted at the cross wall. Apical cell rounded. Reproduction by hormogonia. Typical from saline environment.','Zhou et al. 2018',NULL,0,0),(1085,1128,'description','Thallus blue-green. Filaments not branched, straight or curved to floating mats, 1.49–2.27 μm wide. Sheaths firm, thick, covered the trichomes. Trichomes not attenuated at the end. Distinctly constricted at the crosswalls. Cells longer than wide, 1.53–2.37 μm in length and 0.93–1.44 μm in width. Apical cell 1.38–2.43 μm in length, 0.79–1.48 μm in width, and without calyptra. Thylakoids in parietal arrangement, varying from four to five. Gas vesicles absent. No heterocytes. Reproduction via hormogonia.','Zhou et al. 2018',NULL,0,0),(1086,1133,'diagnosis','Filaments single, or forming loose aggregations amongst littoral vegetation; straight or slightly flexuous. Sheath colourless, hyaline, lamellated when mature, open at the apex. Trichomes isopolar, cylindrical, not or slightly constricted at the cross walls. Vegetative cells discoid, 7–10 × broader than long; contents finely granular, without aerotopes; apical cell rounded, without calyptra or thickened outer cell wall. Reproduction by motile hormogonia formed by necridia, or by diagonal fragmentation without the formation of necridia.','McGregor &amp; Sendall 2019',NULL,0,0),(1087,1134,'diagnosis','Filaments single, or forming loose aggregations amongst littoral vegetation; straight or flexuous, up to 21 μm wide. Sheath colourless, hyaline, lamellated when mature, open at the apex. Trichomes isopolar, cylindrical, not or slightly constricted at the cross walls. Vegetative cells discoid, 7–10 × broader than long, 1.7–2.5 μm long × 15.7–17.8 μm wide; contents finely granular, without aerotopes; apical cell rounded, without calyptra or thickened outer cell wall. Reproduction by motile hormogonia formed by necridia, or by diagonal fragmentation without the formation of necridia.','McGregor &amp; Sendall 2019',NULL,0,0),(1088,1135,'description','Thallus mucilaginous, dark blue–green. Filaments densely entangled, 13.2–16.8 μm wide. Sheaths facultative, attached to trichomes, firm, thin, colourless. Trichomes motile, cylindrical, not attenuated, not constricted to slightly constricted at the ungranulated or slightly granulated crosswalls, 9.6–16.8 μm wide. Cells 0.4–0.9 time longer than wide, 4–12.8 μm long. Cell content blue–green, homogeneous to finely granulated. Apical cell rounded, without calyptra.','Martins &amp; Branco 2016',NULL,0,0),(1089,1138,'description','Thallus forming extensive fasciculate mats or small clusters, brown, brown-green, olive-green to darkgreen, dark blue-green to black. Filaments straight, isopolar, unbranched, (8-) 12-30 (-46) μm diam. Sheaths hyaline or bright yellow to yellow-brown, firm, thin or thick, sometimes lamellated. Trichomes not or slightly constricted at the cross-walls, not or slightly attenuated towards ends, (6.6-) 10-21 (-24) μm diam., sometimes some trichomes become contorted to originate the necridial regions. Cells 1.4-5.6 (-6) μm long, 1.2-11 times wider than long. Cross-walls often granulated, sometimes with large granules. Apical cells rounded, conical, conicalrounded, flat-rounded, truncate, rarely capitate, sometimes thickened, without calyptra. Hormogonia formed by fragmentation perpendicular to the longitudinal axis of the trichome helped by necridic cells, or in diagonal position, in this case helped or not by necridic cells.','Caires et al. 2018',NULL,0,0),(1090,1139,'description','Thallus fasciculate, forming extensive mats, brown. Filaments straight, 14-16.4 μm diam. Sheaths hyaline, thin or slight thick, firm. Trichomes cylindrical, slightly constricted at the cross-walls, andsometimes slightly attenuated towards ends, 12.1-14.6 μm diam. Discoid cells, 1.7-2.5 μm long, 5.8-7 times wider than long. Cell content dark-green, granulated. Crosswalls granulated, sometimes with large granules. Apical cells rounded, conical-rounded, conical, flat-rounded, without thickening. Hormogonia formed by cross-wise diagonal fragmentation of the trichome, helped or not by necridic cells.&nbsp;<br><strong>Ultrastructural notes:</strong> Thylakoidal membranes presented parietal or irregular arrangement, which are distributed in different regions of the cell; cyanophycin granules occurred frequently near the cross-walls. Gas vesicles were observed usually in the inter-thylakoid space, frequently forming irregular clusters (aerotopes) near the cell wall and cross-wall.','Caires et al. 2018',NULL,0,0),(1091,1142,'description','Thalli are microscopic in nature and in liquid media, growing as blue-green mats on the bottom of an Erlenmeyer flask or attached to its walls. Filaments entangled, unbranched, with motility. Sheath rare, hyaline, &nbsp;inconspicuous, attached to the cells. Trichomes flexuous, constricted, slightly attenuated towards ends. Vegetative cells longer than wide and/or subquadratic, 1.3–2.5 μm long, 1.7–2.0 μm wide. Terminal cell cylindrical with rounded apex or conic. Involution cells detected.','Genuário et al. 2018',NULL,0,0),(1092,1141,'description','Thalli microscopic, filaments entangled, unbranched, with motility; sheath rare, hyaline, inconspicuous, attached to the cells; trichomes uniseriate, isopolar, slightly attenuated towards ends; vegetative cells longer than wide and/or subquadratic. Hormogonia present. Necridial cells and gas vesicles absent. Involution cells detected.','Genuário et al. 2018',NULL,0,0),(1093,1143,'description','Thallus macroscopic, purple-brown in nature (and culture), growing in mats on granite substrate. Filaments often in fascicles, straight or bent, slightly tapering, false branched. Sheaths purple-brown (fresh isolates and in culture, later colorless), distinct, firm, up to 3.5 μm wide, seldom layered at the basal part near the false branching. Trichomes straight, bent, constricted at cross walls. Cells usually flattened to almost isodiametric, green to blue-green or brownish with peripheral chromatoplasm and central nucleoplasm, frequently granulated, highly vacuolated, 3.2-8.6 μm long × 12.1-20.2 μm wide, apical cells rounded without calyptra. Heterocytes common, intercalary single or in pairs, occasionally flattened but typically square to hemispherical, 5.7-10.1 μm long × 16.7-18.2 μm wide, akinetes not present. Reproduction by hormogonia and fragmentation of trichomes via necridic cells. Meristematic zones if present usually short and located near the apices.','Villanueva et al. 2019',NULL,0,0),(1094,1144,'description','Thallus macroscopic, blue-green, in mats on granite substrates. Filaments straight or bent, solitary or in dense clusters, variably false branched with scytonematoid, tolypotrichoid as well as rivulariacean solitary branching. Sheaths colorless in culture and as fresh samples, distinct, firm, up to 3.5 μm wide, seldom layered at the basal part near the false branching, opened and layered at the apical part. Trichomes straight, bent, or undulated inside the sheath, constricted at cross walls, slightly tapering at the ends. Cells green to blue-green, flattened or barrel-shaped, frequently granulated, non-vacuolated, 3-4.5 μm long × 9-10.5 μm wide at basal part, 2-3.5 μm long × 6.5-7.1 μm wide at the apical part, apical cells rounded or conical. Heterocytes common, typically spherical or hemispherical, 5.1-5.4 μm long × 7.8-8.9 μm wide, often basal, sometimes developing intercalary in pairs before trichome breakage and formation of heteropolar arrangement of trichomes, akinetes not present. Reproduction by hormogonia and fragmentation of trichomes using help of necridic cells. Meristematic zones if present usually short and located near the apical or basal parts.','Villanueva et al. 2019',NULL,0,0),(1095,772,'description','Filaments solitary or few parallel situated in small groups, thick (over 10 μm wide), creeping on the substrate (on mosses, aquatic plants or aerophytic on bark of trees), flexuous, heteropolar or seemingly isopolar, enveloped by thin, firm, sometimes slightly lamellated sheaths; the sheath is closed at the apex or open after hormogonia liberation. Filaments are simple, with rare false branching of coleodesmoid type, ma-ximally two joined parallel together; the branches grow after separation from the mother trichome ± parallel to the mother filament. Trichomes strictly cylindrical along the whole length, not attenuated towards ends, not constricted at cross–walls. Cells cylindrical, always shorter than wide, blue–green, pale blue–green, olive–green, yellowish or violet; apical cells widely rounded, without calyptra. Heterocytes basal, solitary, arise on the basis of young filaments and young branches, usually hemispherical; occasionally develop barrel–shaped or cylindrical intercalary, solitary heterocytes. Akinetes not known. Reproduction by hormogonia, separation of false branches and by fragmentation of filaments.','Sant Anna et al. 2010',NULL,0,1),(1096,698,'description','Filaments solitary or few parallel situated in &nbsp;small groups, thick (over 10 μm wide), creeping on the substrate (on &nbsp;mosses, aquatic plants or aerophytic on bark of trees), flexuous, &nbsp;heteropolar or seemingly isopolar, enveloped by thin, firm, sometimes &nbsp;slightly lamellated sheaths; the sheath is closed at the apex or open &nbsp;after hormogonia liberation. Filaments are simple, with rare false &nbsp;branching of coleodesmoid type, ma-ximally two joined parallel together; &nbsp;the branches grow after separation from the mother trichome ± parallel &nbsp;to the mother filament. Trichomes strictly cylindrical along the whole &nbsp;length, not attenuated towards ends, not constricted at cross–walls. &nbsp;Cells cylindrical, always shorter than wide, blue–green, pale &nbsp;blue–green, olive–green, yellowish or violet; apical cells widely &nbsp;rounded, without calyptra. Heterocytes basal, solitary, arise on the &nbsp;basis of young filaments and young branches, usually hemispherical; &nbsp;occasionally develop barrel–shaped or cylindrical intercalary, solitary &nbsp;heterocytes. Akinetes not known. Reproduction by hormogonia, separation &nbsp;of false branches and by fragmentation of filaments.','Sant´Anna et al. 2010',NULL,0,0),(1097,1145,'description','Strato caespitoso immerso orbiculari, atro-fusco, usque ad 2 millimetr. lato; fllis 1 decimillimetr longis, 5-7 u crassis, pseudo-ramosis; pseudo-ramis facillime deciduis; vaginis arctis, tenuissimis, aureo-fuscis vel hyalinis, fragillimis, tubulosis continuis; trichomatibus 4-5 u crassis, torulosis, olivaceis; articulis diametro paulo brevioribus; heterocystis basilaribus solitariis aureis (v. v.).','Bornet et Flahault 1888',NULL,0,0),(1098,1152,'description','Filaments solitary or in mats, straight or undulate, &nbsp;occasionally &nbsp;falsely &nbsp;branched &nbsp;(Scytonema type); sheaths usually colorless, distinct, firm, thin or thick, &nbsp;seldom &nbsp;intensely &nbsp;colored &nbsp;(brownish &nbsp;to &nbsp;black). &nbsp;Trichomes &nbsp; unconstricted &nbsp; or &nbsp; slightly &nbsp; constricted &nbsp; at &nbsp; cross–walls, without meristematic zones, occasionally two tightly attached in a common sheath (Blennothrix type). &nbsp;Cells &nbsp;rectangular, &nbsp;isodiametric &nbsp;to &nbsp;longer &nbsp;than &nbsp;wide. Apical cells rounded to conical. Reproduction by disintegration &nbsp;into &nbsp;short &nbsp;parts &nbsp;(hormogonia), &nbsp;usually &nbsp;by the help of necridic cells.','Dvořát et al. 2017',NULL,0,0),(1099,1153,'description','Thallus green, blue–green or blackish in fine mats or aggregates, filaments long, straight, bent to &nbsp;undulated, &nbsp;4.15±0.52 &nbsp;μm &nbsp;in &nbsp;diameter, &nbsp;occasionally &nbsp;falsely branched (Scytonema type). Sheath usually col-orless, distinct, firm, thin or thick when intensely violet to &nbsp;dark &nbsp;violet, &nbsp;brownish &nbsp;to &nbsp;black. &nbsp;Trichomes &nbsp;uncon-stricted &nbsp;or &nbsp;slightly &nbsp;constricted &nbsp;at &nbsp;cross–walls, &nbsp;without &nbsp;meristematic &nbsp;zones, &nbsp;occasionally &nbsp;two &nbsp;tightly &nbsp;attached &nbsp;in &nbsp;a &nbsp;common &nbsp;sheath &nbsp;(Blennothrix &nbsp;type). &nbsp;Cells &nbsp;rectan-gular, isodiametric to longer than wide, 3.74±1.34 μm length, &nbsp;2.8±0.46 μm &nbsp;width, &nbsp;blue–green &nbsp;with &nbsp;distinct &nbsp;peripheral &nbsp;chromatoplasma &nbsp;and &nbsp;inner &nbsp;centroplasma, &nbsp;often granulated. Apical cells rounded to conical. Reproduction by disintegration into short parts (hormogonia), usually by the help of necridic cells.','Dvořák et al. 2017',NULL,0,0),(1100,1049,'description','Filaments straight or flexuous, sometimes with more than one trichome in a common sheath, sometimes forming fascicles of trichomes, without false branching. Sheaths firm, thin, colorless. Trichomes not tapering, not or only slightly constricted at the cross-walls, up to 3.5 μm wide. Cells mostly shorter than wide up to isodiametric.','Mai et al. 2018',NULL,0,0),(1101,1049,'etymology','named for the ruins of the Cartusian Monastery in National Park Slovak Paradise, from which the reference strain was collected','Mai et al. 2018',NULL,0,0),(1102,660,'description','Cells solitary or in more or less spherical or irregular groups, with &nbsp;thin, firm, colourless sheaths, usually periphytic on a variety of &nbsp;aerophytic or submersed substrates. Cells spherical, hemispherical or &nbsp;irregular-rounded, enveloped by sheaths. Without pseudofilamentous &nbsp;stages. Thylakoids distributed usually irregularly throughout the &nbsp;protoplast. Cell wall S-layer of special ribbon-like type found in two &nbsp;strains (Budel &amp; Rhiel 1985).','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1103,660,'reproduction','Cells divide irregularly (in various planes), successively by binary &nbsp;fission and retain usually their irregular shape during the cell cycle; &nbsp;mother cells divide often into daughter cells of different shape and &nbsp;size. Some cells later change into baeocytes (or only some of the cells &nbsp;in a colony); baeocytes few or many, of different number in various &nbsp;species. Waterbury &amp; Stanier (1978) have never found motile &nbsp;baeocytes in Chroococcidiopsis, but this phenomenon does appear &nbsp;temporarily, being dependent on environmental factors (e. g., Andersen, &nbsp;in litt.). Divided cells or single cells sometimes are liberated from &nbsp;irregularly split mucilaginous envelopes (sheaths). Sheaths sometimes &nbsp;gelatinize. Different types of cell division and baeocyte production &nbsp;(large variability) were described by Geitler &amp; Ruttner (1935, &nbsp;fig.12) and Friedmann (1961, fig. 25).','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1104,1154,'description','Cells isolate or forming regular (young, with few cells) or irregular (older, with more cells) colonies with variable number of cells (usually up to 64 cells), sometimes several colonies grouped; colonial envelope thin, firm, colourless; cells usually close to each other within the colony, variable in shape; cell division by binary fission, in two or three planes in successive generations; reproduction by baeocyte formation.','Alvarenga et al. 2016',NULL,0,0),(1105,1155,'description','Solitary cells or, more commonly, microscopic colonies (stratified) with several cells (up to 64 or more), forming multicolonial groups, irregular to squarish in outline, up to 44.2 mm (longer axis: mean 27.1 mm; n=34), with dense, more or less regularly arranged cells, clusters of four cells are recognizable within the older colonies or groups. Colonial envelope sometimes visible, thin, usually tightly surrounding the aggregates, hyaline. Cells rounded when isolate, hemispherical when in pairs, nearly squarish when in dense colonies (mutual pressure) or irregular when dividing or forming baeocytes. Isolate cells 2.1–5.7 mm diameter without sheath (mean 3.7 mm; n=37), 3.6–7.1 mm diameter with sheath (mean 5.4 mm; n=37), cells in colonies 1.3–5.2 mm diameter. Cell content usually brownish, sometimes bright green, with few large granules or finely granular. Baeocytes are short cylindrical rounded or more or less spherical, from 1.7 mm diameter when young, with thin, hyaline sheath when a little older, content is brownish to light green.','Alvarenga et al. 2016',NULL,0,0),(1106,1156,'description','Filaments in groups not surrounded by abundant mucilage or gelatin, without radial disposition, entangled, long; branches rare; sheath present, usually thin and hyaline, opened at the apex; trichomes heteropolar, usually constricted; cells of variable length, shorter or longer than wide; heterocytes basal or intercalary, single or in pairs, variable in shape; necridia present; akinetes absent; phyllosphere inhabitant.','Alvarenga et al. 2016',NULL,0,0),(1107,1157,'description','Filaments in groups (culture), up to 535 um long, 3.2–13.0 um diameter (mean 6.49 um; n=112), commonly narrowed towards the ends, rarely branched. Sheath usually thin (widened and lamellate sheaths occasionally found), firm, colourless, lamellate, opened at the apex of the adult filament. Trichomes long and sharply narrowed towards the ends in older trichomes, short but not so evidently attenuated in young ones (cylindrical trichomes are not rare), distinctly constricted at cross-walls, without hairs. Cells 1.7–8.1 um long (mean 4.6 um; n=138), 4.1–8.5 um diameter (mean 6.1 um), length/diameter ratio from 0.3 to 1.3 at swallowed region; 1.5–6.0 um long (mean 3.0 um), 3.5–6.1 um diameter (mean 4.7mm), length/diameter ratio from 0.3 to 1.2 at the middle of trichomes. Cell content blue-green to light green, centroplasm and chromatoplasm evident, large granules present.','Alvarenga et al. 2016',NULL,0,0),(1108,1158,'description','Thallus caespitose or cushion-like, 5 mm high, blackish green, not slippery to the touch (Fig. 2A). Older, basal, &nbsp;colony filaments prostrate on substrate with vertically erect tight loops (Fig. 2, B–C). Filaments isopolar, 11.7–21.35 um wide, not attenuated. Sheath thick, firm, lamellated with divergent layers, hyaline to ochre, with closed apex. Ascendant tight loops with trichomes in common sheath (Figs. 2, B–F and K; 3A; Fig. S1, A–D, F, G and I), occasionally breaking at the tip forming geminate false branches (Fig. S1B). Trichomes straight to coiled (Fig. S1D), spiral or only curved, cylindrical, torulose in parts and constricted at cross walls (Figs. 2, D–I and 3B; Fig. S1I), 3.2–7.3 um wide. Cells cylindrical or barrel-shaped, green to blue- green, 1.5–(2–3.3)–5.7 um long (Figs. 2, G–I and 3D). Heterocytes intercalary, compressed-discoid, hemispherical when terminal due to breakage, (1.6–3.8)–7 um long, (4.2–8)–10.4 um wide (Fig. 2, G–I). Necridia rare to common, single or in pairs (Fig. 2B), 2 lm long, 10 lm in diameter. Hormogonia isopolar. TEM images showing thylakoids with irregular arrangement (Fig. 3, C and D), cyanophycin granules, polyphosphate bodies, carboxysomes, and other subcellular structures (Fig. 3, C and D).','González-Resendiz et al. 2018',NULL,0,0),(1109,1159,'description','Filaments in culture straight to flexuous, isopolar or rarely heteropolar (Fig. 4, B–G), with short loops quickly developing into geminate false branches (Fig. 4K), 4.8–7.2 lm in diameter. Sheath hyaline (Fig. 4, B–I) to ochre (Fig. 4, J and L). Trichomes constricted at cross walls, blue-green at first, later olive to brownish ochre (Fig. 4, B–L), (1.5)–2.0–3.3 um diameter. Cells with granulose content, shorter than wide, (1.5)–2.0–3.3 um wide, (1.1)–2.6–4.8 um long. Hormogonia isopolar (Fig. 4, D–F, J), rounded, and later sometimes heteropolar through attenuation or formation of protoheterocytes at one end (Fig. 4E), abundant, straight to curved, (2.3)–5.9–27 4.8 um long, (1.3)– 2.7–4.8 um in diameter. Heterocytes rare, intercalary, short, 3.3 um long, 2.6 um in diameter. Necridia common, single or up to three (Fig. 4, C and L), 1.3–4.06 um in diameter, 1.2–4.4 um long.','González-Resendiz et al. 2018',NULL,0,0),(1110,1160,'description','Colonies usually olive green to yellow-brownish, forming diffluent mucilaginous, filaments densely entangled, &nbsp;aggregated &nbsp;into &nbsp;macrocolonies &nbsp;(up &nbsp;to &nbsp;0.5 &nbsp;cm &nbsp;in &nbsp;diameter). &nbsp;Vegetative &nbsp;cells &nbsp;barrel-shaped &nbsp;to &nbsp;oval, &nbsp;2.48–(3.71)–4.4 μm long, 2.65–(3.14)–3.97 μm wide [L: W ratio 1.14 (± 0.13)]. Heterocytes usually intercalary, sometimes terminal due to fragment at intercalary heterocytes, solitary, spherical to oval, 3.97 (±0.7) μm long, 3.54 μm wide [L: W ratio 1.12 (± 0.13)]. Akinetes usually in long chains, oval, 7.94 μm long, 5.59 μm wide [L: W ratio 1.45 (±0.2)]. Hormogonia oval, motile, straight, not as densely entangled as vegetative filaments.','Cai et al. 2018',NULL,0,0),(1111,186,'description','Thallus thin, delicate, mostly bright blue–green, diffluent, sometimes fascicle–like, usually forming thin mats; occasionally isolated trichomes. Sheaths absent. Trichomes ± parallel–arranged, cylindrical, straight, slightly flexuous, not constricted at the cross–walls, bent and spherically capitate at the ends, motile, with intense gliding in the direction of the longitudinal axis, sometimes accompanied by a distinctive rotation, 1.5–3 μm wide. Cells rarely short, up to 2–4(6) × longer than wide, 3.5–8 μm long, pale grayish, blue–green or bright blue–green, without evident chromatoplasma or centroplasma, sometimes with translucent cyanophycin granules at the cross–walls, without aerotopes. Apical cells in developed trichomes bent or/and apparently spherical–capitate. Thylakoids concentrically arranged, peripheral and more or less parallel to the longitudinal cell walls, forming a wavy concentric inner cylinder. Centroplasma includes droplets of polyphosphates, starch and carboxysomes (Fig. 3, A–D). The main diacritic features are trichomes lacking sheaths and particularly the morphology of the end cells that are bent, sphe-rically capitate, and elongated up to 15 μm when mature. Reproduction by disintegration of trichomes into motile hormogonia, without necridic cells.','Strunecký et al. 2017',NULL,0,0),(1112,1162,'description','Colony (thallus) spreading, with bundles of filaments, sometimes forming coils, bright green to blue–green, olive when old, not mucilaginous. Trichomes up to 1 mm long, intensely motile, slightly bent and entangled, slightly constricted at the distinct cross–walls, 2–2.3 μm wide. Cells 2–4× longer than wide, pale grayish, blue–green or bright blue–green, without evident chromatoplasma or centroplasma, with translucent cyanophycin granules at the cross–walls, (3)3.5–8 μm long. The main diacritic feature is morphology of trichomes without sheaths and particularly the shape of the end cells, which are in developed stages attenuated and elongated, narrowed, bent, spherically capitate, up to 15 μm long.','Strunecký et al. 2017',NULL,0,0),(1113,728,'description','Colonies (thallus) spreading, mounded, in cultures penetrating the agar, with rings of trichomes visible as minute coils in the colony, blue–green, dark green, pale olive–green to orange. Sheaths absent. Trichomes thin, bright blue–green, usually straight or slightly bent, dispersed evenly and loosely without mat formation, unconstricted or only indistinctly constricted at the cross–walls, 1.3–2.2 μm wide, slightly attenuated and bent at the ends, motile with gliding motility. Sheaths absent. Cells pale olive–green to bright blue–green, sometimes with orange granules at the cross–walls, 2–4× longer than wide, 4–8 μm long. Apical cells (developed) cylindrical rounded and elongated, conical, sometimes bent or hooked, never calyptrate. Necridic cells not observed. Thylakoids parietal with generally straight four to five layers of thylakoid membranes. Thylakoids in transversal section with triangle or rhombic organization (Fig. 3G). Numerous polyphosphates of variable size were found, mainly at the peripheral part of the cells (e.g., Fig. 3I).','Strunecký et al. 2017',NULL,0,0),(1114,108,'description','Trichomes are isopolar, cylindrical, spirally coiled or straight (Fig. 1, Fig. 2a–c). Trichomes of both types (spirally coiled and straight) are motile, unsheathed or with a thin, inconspicuous sheath, not or only slightly constricted at the cross walls and with rounded apical cells lacking calyptra or thickened cell wall (Fig. 1e–i; Fig. 2a,b). Cells of both trichome types are shorter than they are wide; 6–8 μm wide, 2.6–5.6 μm long. Both types of trichomes possess granulation at cross walls (Fig. 1g–i).','Nowicka-Krawczyk et al. 2019',NULL,0,1),(1115,1164,'description','Trichomes are isopolar, cylindrical, spirally coiled or straight (Fig. 1, Fig. 2a–c). Trichomes of both types (spirally coiled and straight) are motile, unsheathed or with a thin, inconspicuous sheath, not or only slightly constricted at the cross walls and with rounded apical cells lacking calyptra or thickened cell wall (Fig. 1e–i; Fig. 2a,b). Cells of both trichome types are shorter than they are wide; 6–8 μm wide, 2.6–5.6 μm long. Both types of trichomes possess granulation at cross walls (Fig. 1g–i).','Nowicka-Krawczyk et al. 2019',NULL,0,0),(1116,1164,'eco_distro','Benthic mats in standing waters in temperate zones with optimum growth between pH 6.8 and 7.5, and electrical conductivity between 250 and 445 μS.cm<sup>−1</sup>','Nowicka-Krawczyk et al. 2019',NULL,0,0),(1117,681,'diagnosis','Filaments solitary without sheaths, or with very fine, facultative and diffluent sheaths, sometimes with several to many trichomes associated more or less in parallel without common firm sheaths. The fascicles are not enveloped in slime. Trichomes simple, cylindrical along their whole length (up to the end), uniseriate, pale bluegreen, slightly constricted or unconstricted at cross-walls, motile, (2.5) 3–5 (5.3) μm wide. Cells isodiametric or slightly longer or shorter than wide. End cells rounded, bent and hooked without calyptra, 2–3 end cells usually bent or folded from the longitudinal axis, with distinct movement. All cells are capable of division (without meristematic zones). The cell content is heterogenous, sometimes with a slightly more distinct peripheral chromatoplasma. Arrangement of thylakoids in cells is parietal or semiparietal with a circular pattern containing bundles of thylakoids, crossing the interior of cells. Solitary granules of polyphosphate and cyanophycin are present in cells. Comparison of 16S rDNA revealed it is phylogenetically similar (95%) to the Microcoleus vaginatus cluster, whereas its similarity when compared with all the other orders of cyanobacteria is under 93% (Table 3).','Strunecký et al. 2014',NULL,0,0),(1118,1166,'diagnosis','Trichomata singularia vel relaxata aggregata, liber natantia. paene recta vel paulo concurvata aliquando laxe complicata, non vel paulo constricata ad septa, non vel rarius attenuata ad apices, 11.7-16.6 um lata, ad 23 mm longissima in culturis. Trichomata interdum volubilia inter se quasi funiculosa. Trichomata caeruleoviridia vel olivácea, sine phycoerythrin. Cellulae disciformes 2.6-4.1 um longae. Cellulae ad apices rotundatae vel deplanatae et rotundatae, nullae calyptrae. Vesiculae gaseosae minutae spargentes in protoplasmate. Thylacoides dispositae irregulariter transversim protoplasmate toto. Vagina percuam tenuis et translucens, solum in culturis interdum observata. utcunque absens in cellulis naturalibus. Neque pseudoramosa neqiie heterocystae et akinetes praesens in trichomatc. Reproductio trichomatibus fragmentât ione ad cellulas<br>necridium. Conipositio acido pingtii typus 2.','Thu et al. 2012',NULL,0,0),(1119,1023,'description','Trichomes blue-green or olive-green in colour, solitary or in loose clusters, and free-floating. Trichomes almost straight or slightly waved and sometimes gently folded, not or slightly constricted at cross-walls, and not or rarely attenuated towards the end cells. Occasionally, a very thin and fine sheath in culture. Arrangement of thylakoids irregular. Reproduction by the help of necridic cells.','Thu et al. 2012',NULL,0,0),(1120,706,'description','Main filaments creeping, forming attached irregular disks on the underside of leaves of aquatic plants, more or less radiating from the center of the colony, sometimes biseriate to multiseriate, typically branching mostly to one side. Sheath colorless, homogenous. Trichomes monoseriate to multiseriate, tapering towards filament apices. Cells in main filaments compressed spherical to almost spherical. Cells in branches becoming longer than wide and cylindrical. End cells separated from subterminal cells, forming a dehiscent cap like structure at the end of branches. Heterocytes present, mostly intercalary, rarely lateral. Akinetes present, in masses within the main filaments. Hormogonia released from tips of branches.','Wilde et al. 2014',NULL,0,0),(1121,763,'description','Main filaments creeping, forming attached irregular disks on the underside of leaves of aquatic plants, more or less radiating from the center of the colony, sometimes biseriate to multiseriate, typically branching mostly to one side. Sheath colorless, homogenous. Trichomes monoseriate to multiseriate, tapering towards filament apices. Cells in main filaments compressed spherical to almost spherical. Cells in branches becoming longer than wide and cylindrical. End cells separated from subterminal cells, forming a dehiscent cap like structure at the end of branches. Heterocytes present, mostly intercalary, rarely lateral. Akinetes present, in masses within the main filaments. Hormogonia released from tips of branches.','Wilde et al. 2014',NULL,0,0),(1122,1167,'description','Thallus macroscopic brown–green mats. Filaments solitary, isopolar, straight, dark blue–green or brown–green, without sheath. Trichomes cylindrical, motile, not constricted or very slightly constricted at the not granulated cross–walls, not attenuated to the ends. Cells 4–6 um in width, shorter than wide or sometimes isodiametric, cell content blue–green, without aerotopes, and apical cells rounded, not tapered, nor capitate, without calyptra, with granular content mainly in older cells. Division by necridic cells and formation hormogonia.','Heidari et al. 2018',NULL,0,0),(1123,1168,'description','Solitary filaments, straight or wavy, with very thin, colorless sheath. Immotile. Trichomes strongly constricted at the cross walls, 1–2 μm wide. Cells isodiametric or longer than wide, 2–5 μm long, with distinct granules at the cross walls. Reproduction with hormogonia.','Heidari et al. 2018',NULL,0,0),(1124,1169,'description','Solitary filaments, straight, with very thin, colorless sheath. Immotile. Trichomes strongly constricted at cross walls, (0.8) 1.0–1.5 μm wide. Cells isodiametric or a little longer than wide, 1.0–2.0 μm long, usually with one prominent granule per cell. Nodules are formed very seldom, of multiseriate filaments were not observed. Reproduction with hormogonia.','Heidari et al. 2018',NULL,0,0),(1125,1170,'description','Filaments straight or wavy, blue–green or olive green. Sheath is thin, inconspicuous. Trichomes cylindrical, isopolar, unbranched, always slightly constricted at cross walls, motile. Cells shorter than wide. The terminal cell is elongated, conical, bent or straight inflated, rounded end without calyptra. Thylakoids have radial arrangement. Aerotopes are not present.','Heidari et al. 2018',NULL,0,0),(1126,1171,'description','Filaments straight, in natural environment forming benthic mats. Trichomes 3–4 (5) μm wide, slightly constricted on cross walls, cells always shorter than wide, terminal cell elongated, conical, bent, never acuminate.','Heidari et al. 2018',NULL,0,0),(1127,1175,'description','Trichomes straight, isopolar, unbranched, blue–green, motile, with a distinctive oscillation, not constricted or slightly constricted at the ungranulated cross–walls, usually attenuated at the ends. No sheath is present. Cells mostly isodiametric or longer than wide, rarely shorter. Terminal cells strongly bent and acute conical to conical, never pointed. Cell content homogeneous or finely granulated.','Heidari et al. 2018',NULL,0,0),(1128,1176,'description','Trichomes solitary, 3–5 um wide, bright blue–green, mostly straight, long, without sheats, intensely motile, not or slightly constricted. Cells isodiametric or longer than wide 3–5 um long. Terminal cell conical, elongated.','Heidari et al. 2018',NULL,0,0),(1129,1177,'description','Filaments solitary, cylindrical along the whole length, straight, with facultative sheath. Sheaths around single trichomes thick, firm, colorless, not lamellate. Trichomes cylindrical, isopolar, constricted at cross walls, not attenuated towards ends, unbranched. Cells up to 4× longer than wide, cylindrical, pale blue–green, with scattered larger granules. Terminal cells rounded at the apex, without calyptra. Reproduction by disintegration of trichome into immotile segments, sometimes with participation of necridic cells.','Heidari et al. 2018',NULL,0,0),(1130,1178,'description','Filaments entangled or fasciculated, flexuous, enveloped by a facultative, thick, homogeneous and colorless sheath, 4 – 6 μm wide. Trichomes cylindrical, straight, blue–green, constricted at cross walls, not attenuated, immotile, 3.5– 4 μm wide. Cells longer than wide, apical cells rounded, without calyptra 5 –14 μm long. Cell content blue–green, homogenous, ungranulated cross wall. Sometimes with large granules in the cells.','Heidari et al. 2018',NULL,0,0),(1131,1180,'description','Trichomes solitary, straight, pale blue green, 1– 2 μm wide, constricted at the cross walls, without sheaths. Cells 2–5 times longer than wide ( 5–8 μm). Without aerotopes. Apical cells cylindrical, rounded.','Heidari et al. <span class=\'fr-marker\' data-id=\'0\' data-type=\'false\' style=\'display: none; line-height: 0;\'>​</span><span class=\'fr-marker\' data-id=\'0\' data-type=\'true\' style=\'display: none; line-height: 0;\'>​</span>2018',NULL,0,0),(1132,1179,'description','Filaments solitary, cylindrical along the whole length, straight, with facultative sheath. Sheaths around single trichomes thick, firm, colorless, not lamellate. Trichomes cylindrical, isopolar, constricted at cross walls, not attenuated towards ends, unbranched. Cells up to 4× longer than wide, cylindrical, pale blue–green, with scattered larger granules. Terminal cells rounded at the apex, without calyptra. Reproduction by disintegration of trichome into immotile segments, sometimes with participation of necridic cells.','Heidari et al. 2018',NULL,0,0),(1133,1183,'description','Most similar to L. boryana and L. foveolarum (Rabh. ex Gom.) Anagnost. et Kom., but with wider filaments, wider trichomes, and tapered hormogonia. Thallus consisting of densely entangled filaments, penetrating the agar, dark dull olive-green in color. Filaments with a single trichome, rarely with 2–3 tight- ly entwined trichomes, with occasional false branching, typically 3.4–4.0 um wide, up to 6.0 um wide when containing more than one trichome. Sheath colorless, diffluent, thin, rarely extending past the trichome apex, occasionally absent. trichomes immotile, very short to over 200 um long, not evidently tapering, but sometimes producing tapered hormogonia, with cell division as in the Pseudanabaenaceae, constricted at the crosswalls, with crosswalls often scarcely visible, lacking necridia, (2.5)3.0–3.5 um wide. Cells nongranular, with 5–7 thylakoid layers peripheral along the outside walls and crosswalls, with centroplasm cylindrical and clearly visible, quadratic or shorter than broad, 1.2–3.5 um long. End cells bluntly rounded, not set apart morphologically from other cells.','Casamatta et al. 2005',NULL,0,0),(1134,1186,'other','<a href=\'https://en.wikipedia.org/wiki/Database_testing\' rel=\'noopener noreferrer\' target=\'_blank\'>Wikipedia: Database testing</a><br><strong>Database testing</strong> usually consists of a layered process, including the <a href=\'https://en.wikipedia.org/wiki/User_interface\' title=\'User interface\'>user interface</a> (UI) layer, the business layer, the data access layer and the database &nbsp;itself. The UI layer deals with the interface design of the database, &nbsp;while the business layer includes databases supporting <a href=\'https://en.wikipedia.org/wiki/Strategic_management\' title=\'Strategic management\'>business strategies</a>.','Říha 2019',NULL,0,1),(1135,1187,'description','Trichomes attenuated, solitary, unbranched, blue-green (appeared as mats), cells 1.5–2.5μm long and 2.03–2.45μm in width, slight constrictions in the crosswalls, apical cells sharply pointed, always without any crosswalls and without calyptra, facultative and firm mucilaginous sheath, motile (gliding movement). Reproduction occurs vegetatively by the disintegration of hormogonia (short filaments). Akinetes, gas vacuoles, heterocytes absent, thylakoids radially arranged.','Chakraborty et al. 2018',NULL,0,0),(1136,1089,'description','Thallus fasciculated, blue–green. Cylindrical and straight trichomes, slightly attenuated, sometimes bent at the end, unconstricted or slightly constricted at the crosswalls, facultative hyaline and firm sheath, attached to trichome or wider. Cells wider than long, 2.0–3.4 (mean 2.6) um long, 4.2–6.5 (mean 5.2) um wide. Apical cell strongly or slightly capitate, sometimes with conical calyptra, cell content with facultative aerotopes. Hormogonia formation by biconcave necridic cells. Thylakoids radially oriented.&nbsp;','Malone et al. 2015',NULL,0,0),(1137,1090,'description','Cylindrical and straight trichomes, bent at the end, slightly attenuated, unconstricted or constricted at the crosswalls, facultative hyaline and firm sheath, narrow or wide. Cells wider than long, 2.0–3.5 um long, 4.8–7.3 um wide. Apical cell slightly or strongly capitate, cell content with facultative aerotopes. Hormogonia formation by biconcave necridic cells.','',NULL,0,0),(1138,1091,'description','Cylindrical and straight trichomes, bent at the end, slightly attenuated and constricted at the crosswalls, hyaline and firm sheath, attached to trichome or wide. Cells wider than long, 2.2–3.1 um long, 5.6–6.7 um wide. Apical cell strongly capitate with conical calyptra, cell content with facultative aerotopes.Hormogonia formation by biconcave necridic cells.','',NULL,0,0),(1139,696,'description','Thalli live solitary or in small clusters among other algae and cyanobacteria. Simple filaments are heteropolar with a basal heterocyte, later simply Tolypothrix type false branching, rarely binary falsely branched, up to forming creaping isopolar filaments with numerous types of false branching. Filaments cylindrical, usually slightly widened towards ends (also narrowed when forming hormogonia); in narrow parts only (9.8)13.6–16 μm wide, later, especially at the ends up to 30 μm wide. Almost cylindrical filaments can also occur. Sheaths are of different width. When thick, they are densely lamellate, colorless up to yellow–brown mostly in inner parts, outer layers remain often colorless, sometimes partly with calcareous incrustations. Trichomes are uniseriate, of variable width, composed of variously shaped cells. Cells in some parts clearly constricted at cross walls, in terminal parts usually not constricted, sometimes club–like widened, terminal cells rounded. The width of young trichomes ranges from 6 to 10.5 μm, in apical and club–shaped widened segments elder trichomes can be up to 12.4 μm wide. Cells in younger parts are usually barrel–shaped or almost spherical, isodiametric or slightly shorter or longer than wide, in middle parts cylindrical and up to twice as long as wide, and at the ends usually cylindrical and often shorter than wide, bright blue–green. Heterocytes are basal in young germinating filaments, hemispherical or almost spherical, later ovoid, oval or cylindrical, 7.4–22.3 × 5–12.4 μm in diameter. In well developed filaments the heterocytes are spread irregularly between vegetative cells. Akinetes missing; reproduction by hormogonia and usually 1–4 celled hormocytes with densely lamellate, yellow–brown sheaths. Germination of hormocytes proceeds without the heterocyte which appears later during growth of a new filament.','Komárková , Zapomělová et Komárek 2012',NULL,0,0),(1140,775,'description','Filaments solitary or in clusters, at the bases 8.5–12.4 μm wide, at the ends 11–17.4 μm wide. Trichomes 4.5–8.5 μm, at the ends up to 10 μm wide. Trichomes composed of morphologically diverse cells, mostly shorter than wide up to isodiametric, usually clearly constricted at the cross walls. False branching mostly of tolypothrichoid type, branches fan-like divaricated at the ends. Cells barrel-shaped up to almost cylindrical, rarely longer than wide, but mostly shorter up to isodiametric. Filaments often composed of cells of various morphology. Meristematic zones with short cells, occurring usually near the ends of branches. Reproduction mostly by hormogonia.','(Komárek) Komárek, Komárková, VEntura, Kozlíková-Zapomělová et Rejmánková 2017',NULL,0,0),(1141,774,'other','Filaments solitary or in small clusters, among other algae and cyanobacteria. Filaments simple, heteropolar with basal heterocytes, later simply (tolypotrichoidally), rarely binary falsely branched, up to forming creeping isopolar filaments with numerous false branches. Filaments cylindrical, usually slightly widened, or rarely narrowed towards ends; in narrow, lower parts (9.8–)13.6–16 μm wide, later, especially at ends, up to 28 μm wide, almost cylindrical filaments can also occur. Sheaths very thick, densely lamellated, yellow-brown, mostly in inner parts, outer layers generally remain colourless, occasionally \'telescopic\'; dense lamellation usually occurs in upper parts of filaments, resulting in wide, frayed (\'ciliose\') appearance; the sheaths sometimes contain partly calcareous incrustations. Trichomes monoseriate, of variable width, composed of cells with various morphology, in some parts, clearly constricted at the cross walls, in terminal parts usually unconstricted, sometimes club-shaped widened, terminal cells rounded; the width of young trichomes ranges from 6 to 10.5 μm, in apical and club-shaped widened segments the mature trichomes can be up to 12.4 μm wide. Cells in central parts of trichomes are usually barrel-shaped or almost spherical, isodiametric or slightly shorter or longer than wide, in middle parts cylindrical up to 2× longer than wide, at the ends usually cylindrical and often shorter than wide, bright blue-green. Heterocytes basal in young, germinating filaments, hemispherical or almost spherical, later intercalary, ovoid, irregularly oval or cylindrical, 7.4–22.3 × 5–12.4 μm. Akinetes or arthrospores absent, reproduction by hormogonia and usually 1–2-celled, more or less discoidal hormocytes with densely lamellated, yellow-brown sheaths.','Komárková, Zapomělová et Komárek 2013',NULL,0,0),(1142,1190,'description','Colony brownish-black. Filaments heteropolar, with variable morphology along the length of mature filaments, often irregularly coiled or bent (Fig. 4, a–d), with trichomes sometimes becoming so tightly coiled and bent within the sheath that filaments are wider and the continuity of the trichomes is obscured (Fig. 4i), with false branching, particularly in tightly coiled regions of the filament (Fig. 4c), with branching not obviously associated with heterocyte proximity, without sheath (Fig. 4, a, e, and j–l) or enclosed in a thin, firm colorless sheath (Fig. 4, b–f, and i). Basal portions of trichomes often with a terminal, unipolar heterocyte, with subterminal vegetative cells typically distinctly wider than subsequent cells (Fig. 4h), with cells clearly constricted at the cross walls, 4.0–6.0 um wide. Internal portions of some trichomes thinner, slightly constricted to unconstricted at the crosswalls, with elongated cells (Fig. 4, a and d), 2.0–4.0 lm wide, but thallus also with trichomes widened in internal portions, up to 8 um wide, with cells longer than wide to short discoid cells as short as 1.5 um long (Fig. 4l). Apical regions of trichomes mostly thin like internal portions (2.0 um wide) (Fig. 4, f and g) or distinctly<br>swollen (producing hormogonia; Fig. 4, a and e), slightly constricted to strongly constricted at the crosswalls, with cells shorter than wide to isodiametric, 5.0–8.0 um wide. Hormogonia lacking heterocytes, untapered, distinct constrictions at crosswalls, and with cells isodiametric or longer than wide, produced either by fragmentation from apices (cells 3.2–6.0 um long, 8.0–8.8 um wide; Fig. 4k) or presumably by germination from akinetes (cells 4.0–6.0 um long, 2.4–4.8 um wide; Fig. 4j). Vegetative cells blue-green to brownish violet, near heterocytes longer than wide, 8.0–10.0 um long, becoming elongated in the center of mature filaments,<br>up to 30 lm long, and becoming shorter and broad at the swollen apices, 2.0–5.6 um long. Terminal heterocytes hemispherical to long conical, 4.4–14.0 um long, 4.4–8.0 um wide, intercalary heterocytes abundantly produced, cylindrical or barrelshaped (Fig. 4, a and d), 6.0–18.4 um long, 4.4–8.0 um wide. Akinetes not observed.','Hauer et al. 2014',NULL,0,0),(1143,1191,'description','Colony blue-green, thin, spreading from center. Filaments heteropolar, with variable morphology along the length of mature filaments, lacking firm sheath but sometimes enclosed in soft diffluent mucilage (Fig. 5j). Basal portions of trichomes typically with a terminal, unipolar heterocyte (Fig. 5, a, c, d, g, and j), sometimes with a second heterocyte forming adjacent to or 2–3 cells away from the terminal heterocyte (Fig. 5, h and k), with cells clearly constricted at the crosswalls, 4.0–5.2 um wide. Internal portions of mature trichomes becoming thinner, slightly constricted to unconstricted at the cross walls, with elongated cells (Fig. 5, e and h), 3.0–4.0 lm wide. Apical regions of mature trichomes distinctly swollen, slightly constricted to strongly constricted at the cross walls, with cells shorter than wide to isodiametric (Fig. 5, c, f, and j), 5.0–7.0 um wide. Hormogonia lacking heterocytes, with inconspicuous tapering, slight constrictions at crosswalls, and with cells shorter than wide<br>(Fig. 5d). Vegetative cells blue-green, near heterocytes isodiametric to longer than wide, 4.0–7.0 um long, becoming elongated in the center of mature filaments (Fig. 5h), up to 22 um long, and becoming short and broad, or nearly spherical at the swollen apices, 2.6–6.0 um long. Terminal heterocytes spherical and diminutive, 4.0–5.0 um in diameter, becoming enlarged, elongate oval to elongate cylindrical with age, 6.0–24.0 um long, opposite of swollen ends (intercalary when releasing hormogonia), spherical to balloon-shaped, sometimes elongated, homogenous or with a large clear vacuole, length 1.4–17.4 um, 4.0–10.0 um wide. Akinetes<br>sporulate and released as single cells which quickly divide and remain associated with the akinete cell<br>wall (Fig. 5, a and b), 22–24 lm long, 10.0–12.0 um wide.','Hauer et al. 2014',NULL,0,0),(1144,1192,'description','Colony blue-green, thin, spreading from center. Filaments heteropolar, with variable morphology along the length of mature filaments, lacking sheath or sometimes enclosed in firm mucilaginous sheath. Basal portions of trichomes sometimes with a terminal, unipolar heterocyte, with cells clearly constricted at the cross walls, 6.0–7.6 um wide. Internal portions of mature trichomes becoming thinner, distinctly constricted to less frequently slightly constricted at the cross walls, with elongated cells, 2.6–6.0 um wide. Apical regions of mature trichomes thin or very gradually widened, distinctly constricted at the cross walls, with cells longer than wide, 4.8–8.4 um wide. Hormogonia lacking heterocytes, untapered, distinct constrictions at cross walls, and with cells mostly longer than wide, produced by fragmentation from apices, with cells 4.0–10.8 um long, 5.6–6.8 um wide. Vegetative cells blue-green, near basal region shorter or longer than wide, 5.2–7.6 um long, becoming elongated in the center of mature filaments, 5.0–26 um long, and becoming shorter and broad in the apical portion, (2.4)-5.0–14 um long. Basal heterocytes spherical to ellipsoidal, intercalary heterocytes ellipsoidal or oval. Akinetes produced abundantly in series, enlarged, with coarsely granular cytoplasm, 6.4–14 um long, 6.4–9.2 um wide.','Hauer et al. 2014',NULL,0,0),(1145,613,'description','Filaments densely arranged, radiating from the centre of irregularly spherical to discoid, blue-green to olive-green colonies. Filaments isopolar, uniseriate, cylindrical, straight or flexuous, main filament generally wider than the lateral filaments which gradually taper to a bluntly conical end; with single or geminate false-branching. Sheath firm, lamellated, uncoloured to yellowish or yellow-brown, closed at the apex. Vegetative cells isodiametric to shorter than broad, slightly constricted at the cross walls. Heterocytes basal and intercalary, solitary, spherical to compressed-ovoid. Akinetes absent.','McGregor et Sendal 2017',NULL,0,0),(1146,1193,'description','Filaments densely arranged, radiating from the centre of spherical to discoid, blue-green to olive-green colonies, 5–25 mm in diameter. Filaments isopolar, uniseriate, cylindrical, straight or flexuous, 20–39 um in diameter, main filament generally wider than the lateral filaments which gradually taper to a bluntly conical end; with single or geminate false-branching. Sheath firm, lamellated, uncoloured to yellowish or yellow-brown, closed at the apex. Vegetative cells isodiametric to shorter than broad, slightly constricted at the cross walls, 3.3–8.2 um long 18.0–27.5 um wide in the main filament, 3.5–5.0 um long 4.2–12.0 um wide in lateral branches, with granular contents. Heterocytes basal and intercalary, solitary, spherical to compressed-ovoid, 6.3–9.5 um long 11.0–19.0 um wide. Akinetes absent.','McGregor et Sendal 2017',NULL,0,0),(1147,484,'description','Thallus spread in tufts forming woolly mats, dark blue-grey. Sheaths firm, attached to trichomes, not lamellated. Filaments true-branched, commonly with Y-like type of branching, rarely with false branching. Trichomes uniseriate, ± isopolar, with cells shorter or longer than wide, barrel-shaped, cylindrical, slightly and/or distinctly constricted. Heterocytes intercalary and also terminal at the germinating ensheathed hormogonia (hormocytes). Reproduction succeeded by the formation of ensheathed hormogonia that usually grow subaerophytically over the liquid medium. Akinetes not observed.','Lamprinou, Christodoulou, Hernández-Mariné et Economou-Amilli, 2016',NULL,0,0),(1148,485,'description','Thallus woolly, partly growing subaerophytically with densely coiled and/or parallel-arranged filaments. Filaments long, isopolar, very slightly attenuated towards the ends. Sometimes heteropolar young filaments are obvious germinating from hormogonia with a basal heterocyte. Filaments true-branched with a Y-like type of branching, rarely with false scytonematoid branching. Y-type of branching originating from the.oblique division of an intercalary cell followed by a second oblique division perpendicular to the previous one but without lateral displacement of the branch point. Heterocytes intercalary, 5.2–10.7 μm (8.15 μm ± 1.63, n=30) wide and 6.7–15 μm (9.62 μm ± 2.85, n=30) long with a pale yellow content. Mature filaments 7.8–12 μm (9.55 μm ± 0.99, n=30) wide. Branches narrower than the main filament, 4.84–8.1 μm (6.58 μm ± 0.91, n=30) wide. Sheath thin and firm, colorless. Trichomes constricted at the cross walls and extending slightly attenuated at the ends. Cells cylindrical or dolichoform to barrel-shaped, 5.16–13 μm (8.2 μm ± 1.9, n=30) long at the mature filaments, and 8.17–15.6 μm (10.98 μm ± 2.34, n=30) long at the young filaments, with smooth finely granulated content, blue-green to violet-brownish due to the phycoerythrin predominance. End cells more or less rounded. Ensheathed hormogonia 32.74–73.69 μm (53.5 μm ± 11.49, n=30) long and 6.73–9.07 μm (7.88 μm ± 0.76, n=30) wide, maintaining 4–17 cells and growing subaerophytically at the ends or at intercalary sites of the trichomes. Necridic cells sometimes present.','Lamprinou, Christodoulou, Hernández-Mariné et Economou-Amilli, 2016',NULL,0,0),(1149,471,'diagnosis','Filamenta cyanoprocaryotica, in stratum planum aerugineum vel aerugineo-viride agglomerata, recta vel paucim flexuosa, simplicia, cylindrica, sine ramificatione. Vaginae facultativae, tenues, incolores, diffluentes vel adsunt. Trichoma cylindrica, uniseriata, fragilia, ad genicula non vel interdum leviter constricta, in parte apicali ad extremum attenuata et interdum flex a, cum cellula terminali plus minusve aClita vel acute-rotundata. Cellulae isodiametricae vel longiores vel breviores quam lalae. Thylakoidae radialiter dispositae. Heterocytae akinetesque carentes. -Plantae hydrophilae vel subaerophyticae, plerumque halophilae velthermales.','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012',NULL,0,0),(1150,473,'diagnosis','Filamenta in stratum planum aerugineo-viride agglomerata, plus minusve recta vel flexllosa. Vaginae facultativae, tenues, diffluentes. Trichoma fragilia, ad genicula lev iter constricta, 7.5-9 um lata, ad extremum breve attenuata et f7exa, cum cellula apicali subacuta. Cellulae breviores quam lalae ad isodiametricae.','Chatchawan, Komárek, Strunecký, Šmarda et Peerapornpisal 2012',NULL,0,0),(1151,1194,'diagnosis','Stratum atro-viride. Trichomata obscure aeruginea, flexuosa, ad genicula non constricta, 8-9 um crassa, apice curvata, breviter attenuata, acutissiine acuminata et interdum quasi mucronata; articuli diametro trichomatis ad triplo breviores 2,5-3um longi. Dissepimenta granulis protoplasmaticis saape notata; cellula apicalis acuminata ; calyptra nulla.','Gomont 1899',NULL,0,0),(1152,1195,'diagnosis','Trichomata i n stratum rerugineo-viride agglomerata, recta, fragilia, interdum ad genicula leviter constricta, 3 um ad 5 um crassa, apice breviter attenuata acutissime acuminata haud capitata uncinata vel tortuosa ; articuli &nbsp;diametro trichomatis longiores, rarius subquadrati, 5 , 5 um ad 8 um longi ; dissepimenta granulata aut granulis protoplasmaticis totam cellulam implentibus obducta ; cellula apicalis quasi mucronat a ; calyplra nulla','',NULL,0,0),(1153,682,'description','Trichomata in stratum reruginosum agglomerata, recta, fragilia, ad genicula baud constricta, 3 um ad 4 crassa, apice breviter attenuata acutissime acuminata haud capitata uncinata vel torluosa; articuli subquadrati vel &nbsp;diametro ad duplo breviores, 1.6 um ad 5 um longi, protoplasmate tenui-granuloso farcti; dissepimenta passim granulata; cellula apicalis quasi mucronata; calyptra nulla.','Agard ex Gomont 1892',NULL,0,0),(1154,1196,'description','Trichomata in stratum reruginosum agglomerata, recta, fragilia, ad &nbsp;genicula baud constricta, 3 um ad 4 crassa, apice breviter attenuata &nbsp;acutissime acuminata haud capitata uncinata vel torluosa; articuli &nbsp;subquadrati vel &nbsp;diametro ad duplo breviores, 1.6 um ad 5 um longi, &nbsp;protoplasmate tenui-granuloso farcti; dissepimenta passim granulata; &nbsp;cellula apicalis quasi mucronata; calyptra nulla.','Agard ex Gomont 1892',NULL,0,0),(1155,1197,'description','Stratum tenuissi mum, arachnoideum, luteo-viride. Trichomata aureo-viridia, chlorina, recta vel arcuata, fragilia, ad genicula non constricta, 3.5 um ad 4 um crassa, apice recta vel curvula non attenuata; articuli dianmetro trichomatis paulo breviores vel longiores, &nbsp;3.7 um ad 8 um longi, protoplasmate vix granuloso farcti; dissepimenla pellucida, non granulata; cellula apicalis superne rotundala; calyptra nulla (v. v.) .','Kützing ex Gomont 1892',NULL,0,0),(1156,1198,'description','Trichomata aeruginea, in stratum obscure vel atro-aerugnosum agglomerala, eximie recta, fragilia, ad genicula leviter constricta, 5. um ad 8 um crassa, apicem versus longissime et sensim attenuata, ad extremum arcuata vel undulata; articuli quadrati vel diametro longiores, rarissime breviores, 5.4 um ad 8,2 um longi (apicalibus usque ad 14 um longis), interdum granulis protoplasmaticis conspersi; dissepimenta non granulata; cellula apicalis obtusa, haud capitata; calyptra nulla (v. s. ).','Meneghini ex Gomont 1892',NULL,0,0),(1157,1199,'description','Trichomata pulchre aeruginea, in stratum obscure aeruginosum agglomerata, recta, elongata, flexilia, ad genicula vulgo leviter constricta, 4 um ad 6 um crassa, apice haud capitata sub-obtuse et breviter attenuata vel rotundata uncinata; articuli quadrati vel diametro ad duplo breviores, 2.5 um ad 5 um longi; dissepimenta interdum tenue granulata; calyptra nulla (v. v.).','Bory ex Gomont 1892',NULL,0,0),(1158,1201,'description','Stratum tenue, membranaceum, pulchre viride. Trichomata luteole viridia, eximie recta, fragilia, ad genicula leviter, constricta, 3 um ad 5 um crassa, apice breviter attenuata undulata et uncinata, rarius in totum recta; articuli subquadrali, 2.5 um ad 5 um longi . Protoplasma uniformiter granulosum aut dissepimenta punctata; cellula apicalis plus minusve obtusa vel subacuta, haud capitata; calyptra nulla (v. v.)','Crouan ex Gomont 1892',NULL,0,0),(1159,1202,'description','Trichomata in stratum atro-aeruginosum agglomerata, recta, in speciminibus siccis fragilia, ad genicula evidenter constricta, 5.5 um ad 9 um crassa, apicem versus longissime et sensim attenuata undulata et ad extremum uncinatoarcuata; articuli diametro ad triplo breviores, 2.7um ad 4.5 um longi (apicalibus subquadratis, usque ad 8 um longis), proloplasmate tenui-granuloso farcti; cellula apicalis obtusa vel subacuta, haud capitata; calyptra nulla (v. s.)','Agardh ex Gomont 1892',NULL,0,0),(1160,1203,'description','Strato expanso, luteo-viridi, tenui, fere papyraceo. Trichomatibus fere restis vel parum arcuatis, interdum paulo flexuosis, luteo-virescentibus, 4-5.8 um lat., cum vaginatis 4.2-6 um lat., ad genicula leviter vel non contrictis, ad apices evidenter vel rarius vixattenuatis et parum curvatis. Vaginis plerumque parum distinctis, diffluentibus, chlorozincico jodurato non coerulescentibus. Atriculis fere quadratis vel 3-4 um long, id est ad sesquialterum diametro brevioribus, dissepimentis non granulatis. Cellulis apicalibus rotundato vel acutiusculo conoideis sine calyptra.','Elenkin 1949',NULL,0,0),(1161,759,'description','Trichomes free-floating, solitary, straight or slightly arcuate, narrowed towards ends, constricted at the cross-walls, with indistinct mucilaginous envelopes. Cells barrel-shaped, ± spherical or hemispherical, with aerotopes, ± isodiametric or sometimes shorter than wide, 4–8 × 8 um in the trichome centre; apical cells narrowed, end cells slightly elongated, usually 6–8 um long and conical-rounded. Heterocytes solitary, intercalary, spherical, 8–10.2 um in diameter. Akinetes widely oval, with thick, colourless exospore, intercalary, solitary, distant from heterocytes, ±21–24 × 10–20 um','Komárek 2013',NULL,0,0),(1162,760,'description','Trichomes free-floating in plankton, solitary, straight or slightly arcuate, up to more than 1.5 um long, towards ends slightly attenuated, slightly to distinctly constricted at the cross-walls. Cells cylindrical, isodiametric up to 3 × longer than wide, with pale blue-green content with aerotopes, (2.5) 3.5 up to 15 × (2.4) 3–5.1 um; terminal cells up to 3–7 × longer than wide (up to 30 um long), 3–5 um wide, narrowed, at the ends rounded-pointed. Heterocytes spherical to ellipsoidal, (4.4) 6.1–12 × (4.8) 5–8.5 um. Akinetes widely oval, intercalary, mostly distant, rarely joined to heterocytes, (13.6) 18–27.8 × 10.8–15.1 um, with yellow or brownish exospore.','Komárek 2013',NULL,0,0),(1163,761,'description','Trichomes free-floating, solitary, usually very slightly irregularly coiled or flexuous, clearly continually narrowed towards ends, constricted at the cross-walls. Cells shortly barrel-shaped, usually shorter than wide, with &nbsp;facultative aerotopes, up to isodiametric, 2.5–6 × 4.2–5.6 (6.5) um; terminal cells narrowed and elongated, apical cells narrow conical and pointed-rounded. Heterocytes intercalary, solitary, ± spherical, 4.5–6.5 (9) × 5–6.5 (7) um. Akinetes widely oval, intercalary, solitary, distant from heterocytes, (8.4) 13–16 × (9.8) 11–13 um','Komárek 2013',NULL,0,0),(1164,493,'description','Spherical cells, solitary or forming aggregates. Division by binary fission in one plane. Irregular, longitudinal or semi radial arrangement of thylakoids. Presence of long and abundant piluslike structures.','Ramos et al. 2017',NULL,0,0),(1165,692,'diagnosis','Filamenta cyanoprocaryotica, simplicia, libera, solitaria, 5–25 μm lata, vel in fasciculis parvis, fatiscentis, aggregata, recta vel paucim flexuosa, vaginata. Vaginae plus minusve firmae, achroae, hyalinae, tenues vel paucim incrassatae. Trichoma uniseriata, ad dissepimenta non constricta vel paucim constricta, cylindrica, ad apices non attenuata, non distincte calyptrata. Cellulae cylindricae, curtae, semper brevior quam latae, cum vesiculis gaseosis (aerotopis) impletae. Heterocyta akinetesque carentes. Reproductio hormogoniis cylindraceis. – Praecipue natantes in plancto aquis dulcis.','Komárek et al. 2013',NULL,0,0),(1166,796,'description','Filaments cyanoprokaryotic, simple, solitary, free–floating, 5–25 μm wide, or growing in small aggregations, straight or slightly curved, with distinct sheaths. Sheaths firm, colorless, hyaline, thin or slightly widened. Trichomes uniseriate, not or slightly constricted at the cross–walls, cylindrical, not narrowed towards ends, without clear calyptra. Cells cylindrical, short, always wider than long, with facultative gas vesicles<br>(and aerotopes), present in distinct segments of a trichome. Heterocytes and akinetes missing. Reproduction by intense hormogonia production.','',NULL,0,0),(1167,801,'description','Filaments free-floating, straight, rarely curved. Sheaths firm, hyaline, homogeneous. Trichomes not constricted at cross walls, ends rounded but not attenuated. Cells shorter than broad, with many “gas vacuolesů at times. Filaments 24-20 µ wide; trichomes 22-18 µ wide.','Smith 1916',NULL,0,0),(1168,739,'description','Solitary trichomes, in cluster or fine mats, blue–green or dark blue–green (on agar). Filaments solitary or several to many ± parallely arranged, fasciculated, associated in common, colorless, very fine and diffluent slimy &nbsp;envelope; fascicles up to more than 50 μm wide. Single trichomes have facultatively delicate, but firm, colorless, unlamellated sheaths, open at the end. Trichomes straight or slightly curved, not or only slightly constricted at cross walls, (3.1)3.6–5.4 μm wide. Cells quadratic or longer, rarely also shorter than wide, (2.6)3.4–7.2(11) μm long, pale blue–green, with homogeneous, finely granular content, usually with scattered large granules which are sometimes constricted near cross– walls; cross–walls sometimes indistinct. Terminal cells rounded at the ends. Thylakoids ± parietal, fasciculated.','Strunecký et al. 2011',NULL,0,0),(1169,1208,'description','L. filis inter algas varias Myxophycearum libere natantibus, stratum non formatis, flexuosis ; vaginis tenuibus arctissimis et achrois ; trichomatibus laete serugineocoeruleis, inter cellulas non constrictis, apicibus rectis, non attenuatis, obtusis vel rotundato-truncatis; cellulis diametro trichomatis 1 1/2 - 1 3/4 plo longioribus, cytioplasmate homogeneo cum granulis magnis 1 vel 2 prope dissepimenta utrobique aggregatis. Crass, fil. 3.1-3.3 um long, &nbsp;cell. 5-6 um','West &amp; West 1911',NULL,0,0),(1170,740,'description','Filaments entangled or fasciculate, flexuous, enveloped by a facultative, thin, homogeneous and colorless sheath, 3.2–5.6 μm wide. Trichomes cylindrical, straight, blue-green, constricted at the cross-walls, not attenuated, 3.2–5.5 μm wide. Cells isodiametric or slightly longer or shorter than wide, apical cells rounded or conical, without calyptra 2.4–8.8 μm long. Cell content blue-green, homogenous, sometimes with evident chromatoplasm and centroplasm, ungranulated cross-walls. Reproduction by disintegration of trichomes without necridic cells.','Machado de Lima et al. 2017',NULL,0,0),(1171,1021,'description','Colonies hollow, initially rounded, later elongated, usually irregular in outline, composed of many irregular groups of cells; mucilage firm, thick, homogeneous, colourless, hyaline; cells oval or cylindrical with rounded ends, disposed in a single flat or slightly curved layer, on irregular rows, slightly distant from each other, mosaic-like pattern, slightly below the surface of the mucilaginous colonial envelope; without aerotopes; cell division symmetrical by binary fission in one plane perpendicular to the long axis; reproduction by proliferation of daughter colonies from the oldest ones.','Werner et al. 2008',NULL,0,1),(1172,675,'description','Colonies hollow, initially rounded, later elongated, usually irregular in outline, composed of many irregular groups of cells; mucilage firm, thick, homogeneous, colourless, hyaline; cells oval or cylindrical with rounded ends, disposed in a single flat or slightly curved layer, on irregular rows, slightly distant from each other, mosaic-like pattern, slightly below the surface of the mucilaginous colonial envelope; without aerotopes; cell division symmetrical by binary fission in one plane perpendicular to the long axis; reproduction by proliferation of daughter colonies from the oldest ones.','Werner et al. 2008',NULL,0,0),(1173,1021,'diagnosis','Coloniae liberae, natantes, microscopicae, cavae, rotundatae vel elongatae, 62.0-160.0 μm latae, 92.0-340.0 μm longae; vagina firma, homogenea, incolor, hyalina; cellulae ovatae vel teretes apicebus rotundatis, sine singulis mucosis involucris, 1.5-2.3 longiores quam latiores, 2.4-3.8 μm longae, 1.4-2.0 μm latae (in medio 1.68 x 3.06 μm ± 0.18 x 0.45; n = 23); cellulae compactae disppositae in catervis superficie &nbsp;vaginae strato unico; strato plano vel leviter curvato, seriebus irregularibus, liviter distantibus, mosaicis similibus, sitae leviter infra superficiem involucri coloniali mucosi, contentum cellulare viridi-fuscum, homogeneum, sine aerotopis; divisio cellularis plano singulari ad axem perpendicularem; efformatio coloniarum filiarum a coloniis veternis.','Werner et al. 2008',NULL,0,0),(1174,1021,'description','Colonies free-floating, hollow, microscopic, rounded or elongated, 62.0-160.0 μm diameter, 92.0-340.0 μm long;mucilaginous envelope firm, thick, homogeneous, colorless, hyaline; cells oval or cylindrical with rounded<br>ends, without individual mucilaginous envelopes, 1.5-2.3 times longer than wide, 1.4-2.0 μm diameter, 2.4-3.8 μm long (average of 1.68 × 3.06 μm and standard deviation of 0.18 × 0.45; n = 23), disposed in irregular groups, in a single, flat or slightly curved layer, on irregular rows, slightly distant from each other, mosaic-like pattern,<br>slightly below the surface of the mucilaginous colonial envelope; cell content blue-green, homogeneous, without aerotopes; cell division in one plane perpendicular to the long axis; daughter colonies formed from oldest ones.','Werner et al. 2008',NULL,0,0),(1175,1210,'diagnosis','Filaments densely arranged to form blackish-green hemispherical caespitose mats beginning as small 1–4-cm-diameter circular tufts, up to mats 4–6 cm wide by several metres long. Filaments isopolar, cylindrical, straight or flexuous, 15.5–40 um in diameter, densely arranged and erect, often parallely fasciculate, up to 3 cm long, with tolypotrichoid false-branching, rarely with scytonematoid false-branching. Vegetative cells short barrel-shaped or isodiametric, 0.5–1.2 as long as wide, 7.2–16.9 um long, 10.4–14.5 um wide, slightly constricted at the cross-walls, with granulated contents; terminal cells widely rounded. Sheath firm, thick, lamellated, uncoloured to yellowish or yellow–brown in colour, cylindrical, closed at the apex. Heterocytes basal and intercalary, solitary, rarely up to 2(3) in a series, developing particularly at the base of branches, spherical or ovoid, 7.5–16.5 um in diameter, 9.0–24.6 um long. Akinetes not observed. Reproduction by up to 12-celled hormogonia, often with terminal heterocytes, not constricted at cross-walls, separated by necridic cells.','McGregor &amp; Endall 2017',NULL,0,0),(1176,1209,'diagnosis','Filaments densely arranged to form blackish-green hemispherical caespitose mats. Filaments isopolar, cylindrical, straight or flexuous, densely arranged and erect, often parallely fasciculate, with tolypotrichoid false-branching, rarely with scytonematoid false-branching. Vegetative cells short barrel-shaped or isodiametric, 0.5–1.2 as long as wide, slightly constricted at the cross-walls, with granulated contents; terminal cells widely rounded. Sheath firm, thick, lamellated, uncoloured to yellowish or yellow–brown in colour, cylindrical, closed at the apex. Heterocytes basal and intercalary, solitary, rarely up to 2(3) in a series, developing particularly at the base of branches, spherical or ovoid. Akinetes not known. Reproduction by hormogonia, often with terminal heterocytes, not constricted at cross-walls, separated by necridic cells.','McGregor &amp; Sendall 2017',NULL,0,0),(1177,1209,'etymology','The epithet is from the indigenous Ewamian peoples whose traditional lands include Talaroo thermal springs.','McGregor &amp; Sendall 2017',NULL,0,0),(1178,274,'description','Zellen &nbsp; kugelig &nbsp;(durch &nbsp;gegenseitigen &nbsp;Druck &nbsp;kantig), &nbsp;mit &nbsp;dünnen &nbsp;Hüllmembranen, &nbsp; in &nbsp;den &nbsp;drei &nbsp;Richtungen &nbsp; des &nbsp;Raumes &nbsp; sich &nbsp; theilend &nbsp; und &nbsp; zu &nbsp;rundlichen &nbsp; &nbsp;oder &nbsp; unregelmässig &nbsp; traubig &nbsp; lappigen &nbsp; Familien &nbsp; vereinigt. &nbsp; &nbsp; Die &nbsp;sich &nbsp;nicht &nbsp;mehr &nbsp;theilenden &nbsp;Zellen &nbsp;nehmen &nbsp;an &nbsp;Grösse &nbsp;zu, &nbsp;verdicken &nbsp;ihre &nbsp;Membran &nbsp;und &nbsp;ihr Inhalt &nbsp;zerfällt &nbsp; zuletzt &nbsp;in &nbsp;zahl-reiche &nbsp; rundliche &nbsp; Schizosporen. &nbsp; &nbsp; Zeilen &nbsp; und &nbsp; Familien &nbsp; m &nbsp; krustigen &nbsp; Lagern &nbsp; ordnungslos &nbsp; vertheilt. &nbsp;','Hauck 1885',NULL,0,0),(1179,1211,'description','Lager dünn krustenartig, matt schwärzlich. Zellen 5—20 u dick, einzeln und zu 2—4 &nbsp;— vielzelligen, bis 50 —100 u dicken Familien vereinigt; Zellinhalt fast homogen gold- oder rothbräunlich bis schmutzig &nbsp;violett. &nbsp; &nbsp;Hüllmembranen farblos.&nbsp;','Hauck 1885',NULL,0,0),(1180,1211,'description','Colony dark blackish brown, hard, dry, in discrete small clumps, arising from the substrate, consisting of large sarcinoid clusters of coccoid cells, with pseudofilament production uncommon, not obviously divaricately branching, but sarcinoid divaricating clusters may expand outward as they divide radially from a central point, forming compact disc-like expanses. Sheaths colorless, thin, tight, scarcely apparent. Pseudofilaments uni- or multiseriate, 4–8 μm wide when uniseriate, up to 20 μm wide in multiseriate filaments. Cells spherical or more commonly ovoid with sides appressed by neighboring cells, typically in large sarcinoid packets, at first the color of red wine, becoming bluish gray, with mature cells russet-brown to dull copper-brown, with thin cross walls, with few but distinct spherical granules, diameter (2) 4–17(20) μm, sometimes individual cells becoming rounded, enlarged, up to 25 μm in diameter. Chromoplasm often appearing in a parietal position. Baeocytes uncommon, rounded, 3–3.5 μm in diameter.','Shalygin et al. 2019',NULL,0,0),(1181,1211,'eco_distro','Auf Steinen an der Fluthgrenze im adriatischen Meere, der Ostsee und wohl auch der Nordsee.','Hauck 1885',NULL,0,0),(1182,1218,'description','Colonies spherical or ovoid, of four to thrirty-two cells, rarely more, embedded in a copious, hyaline, unlamellated, gelatinous envelope. Cells hemispherical to spherical, with greyish or light blue-green contens, gas vacuoles rarely present. Diameter of cells 7-6.5 um, diameter of colonies up to 60 um.','Smith 1916',NULL,0,0),(1183,1219,'diagnosis','Thallo in superficie cinereo vel luteo-viridi. Filamentis geminis 15- 20 μ crassis, usque ad 400 μ longis. Articulis 4-7 μ crassis, 5- 9 μ longis, ad genicula constrictis, quadratis, cylindricis vel saepissime doliiformibus. Heterocystis sine tegmento circa 9 μ crassis. Vaginis achrois, tenuibus in basali tantum parte saepe luteo-bruneis. Hormogoniis 25- 40 μ longis. Coutentu aerugineoviridi. Habitat in rupibus marinis in pluribus locis orae Dalmatiae mediae.','Ercegović 1929',NULL,0,0),(1184,222,'diagnosis','Strato endolithico, sub superficie irregulariter et late expanso. Thallo &nbsp;composito e filamentis geminis, quae apicali parte in unum unita, &nbsp;basali vero parte attenuata et in acutum et brevem filum protracta &nbsp;speciem ferunt unius tantum filamenti media parte inflexi et ambobus &nbsp;dimidiis arcte intra se adhaerentibus. Filamentis a superficie intra &nbsp;petram verticaliter penetrantibus, divisione vegetativa cellularum &nbsp;intercalarium orientibus, ex una tantum serie cellularum conjunctarum &nbsp;compositis, parallelis, homogeneis, vaginatis, pseudoramosis. &nbsp;Pseudoramis laterali convexione vaginarum et trichomatum orientibus. &nbsp;Vaginis firmis, achrois vel ex parte coloratis. Articulis plus minusve &nbsp;homogeneis, arcte conjunctis. Heterocystis intercalaribus singulis. &nbsp;Propagatio hormogoniis.','Ercegović 1929',NULL,0,0),(1185,1224,'diagnosis','Most similar to K. maculans, from which it differs in having a stratified sheath, thinner thalli, thinner trichomes, and shorter cells (Table 1). Differing from K. dalmatica by its epilithic habit and stratified sheath (Table 1). Differing from both species in the absence of false branches and thalli and smaller cell dimensions (Table 1).','León-Tejera et al. 2016',NULL,0,0),(1186,1224,'description','In natural populations—thalli blue-green, crustaceous, flat, soft, forming neatly delimited and commonly abundant freckle or mole-type colonies 0.5 to 1.0 cm in diameter, less frequently forming longer mat-like colonies up to a few centimeters long, 60–80 μm high. Filaments arranged in tight parallel series, isopolar, forming sharply bent loops in the lower part (Fig. 1 A, B, D, F), with distal ends always directed and attenuated towards the upper part of the thallus (Fig. 1 A, C, E), to 60 μm long from the basal loop to the terminus. Colonial mucilage firm, generally colorless (Fig. 1 E–G), but sometimes yellowish or brownish in the upper surface of the crust (Fig. 1 A), lamellated (Fig. 1 H, Fig. 2 A, B, H), maintaining the integrity of crustose thalli in intertidal populations subject to battering waves at high tide and drought at low tide. Individual sheaths enclosing and binding both parts of a single bent trichome, producing an evident external layer for each paired portion of a single trichome (Fig. 1 H, 2 H, 3 C, H), embedded in the common mucilaginous matrix (Fig. 3 A–C, H). Trichomes constricted at cross walls (Fig. 2 A–G), (1.2) 2–3 (5) μm wide. Cells variable in form, commonly cylindrical or subspherical, sometimes having the shape of a truncated cone, or extremely irregular with different values of length and diameter within a single cell (Fig. 1 B–F. Fig. 2 B, C, D, E), (1) 1.5–3 (6.) μm long. Hormogonia isopolar or heteropolar (Fig. 3 D–G, L), liberated through the upper surface, after release soon becoming bent and somewhat attenuated before heterocytes are differentiated (Fig. 1 G. Fig. 2 A, B. Fig. 3 F–G, K). Heterocytes solitary, intercalary, mostly cylindrical to quadrate, 1.8–3.1 μm in diameter (Fig. 1 B–E), shorter to longer than wide ((1.5) 3–4 (10) μm long); near the apices and sometimes after release of attenuated trichome segments (heteropolar hormogonia) have subspherical shape, 3 μm in diameter (Fig. 2 C–F).&nbsp;<br>In cultures (C708, C695)—thalli soon (1–2 weeks) losing typical parallel disposition of filaments (Fig. 3 A–B). Hyaline sheaths surrounding single trichomes difficult to distinguish, gelatinized, remaining evident around pairs of trichomes (Fig. 3 A–C, H). Trichomes contorted, conserving constricted cells of a wide range of cell shape and sizes (3–10 μm wide), terminally attenuated (Fig. 3 A, C–D, G). Hormogonia commonly short, one to few-celled (4–10 μm long), straight or curved or folded, attenuated or not (Fig. 3 D–G). Cells with big pigmented granules (Fig. 3 A–H).','León-Tejera et al. 2016',NULL,0,0),(1187,1041,'description','Colony reddish brown or brown in actively growing cultures, turning olive-green as culture senesces (Fig. 14a). Filaments long, without false branching, 2.0–2.6 (3.4) μm wide. Sheath firm, thin, colorless, up to 0.8 μm wide (Fig. 14c). Trichomes not or slightly constricted at distinct cross-walls, without necridia, lacking meristematic zones, with cell division occurring throughout the length of the trichomes, 1.7–2.1 μm wide. Hormogonia absent. Cells mostly longer than wide (Figs. 14b, d), rarely isodiametric after division, with parietal thylakoids, with up to three granules usually in the middle of the cell, (2.1) 2.9–3.8 (5.4) μm long. End cells untapered, rounded. D1-D1’ helix 64 nucleotides long, with basal side loop of 7 nucleotides (5’-CAUCCCA-3’), at mid-helix with one large internal loop at position 14–17/41–44, one pair of mismatched nucleotides at position 9 on the 5’ strand (U/U) and one sub-terminal internal loop at 23–24/34–35 immediately separated from the terminal loop by a 5’-GC:GC-3’ clamp. Terminal loop of 5 nucleotides, terminal sequence 5’-AUAGU-3’ (Fig. 6i). Box B 34 nucleotides long, with one basal internal loop at position 5/27–28 and one unpaired adenine residue at position 9 of the 5’ strand (Fig. 7h). V2 helix 18 nucleotides long, unique in sequence and shape, terminal loop of 4 nucleotides, sequence 5’-UUUG-3’ (Fig. 8f). V3 helix was not reported as the sequence from NCBI terminated before the end of the ITS region.','Mai et al. 2018',NULL,0,0),(1188,1225,'diagnosis','Morphologically and ecologically quite distrinct than other validly described soil-borne species of the genus <em>Leptolyngbya </em>with very thin trichomes with constriction; cells cylindrical, longer than broad; cell division transverse, daughter cells divided and attained full length before next division; absence of false branch and necridic cell; apical cells subobtuse to obtuse when older. The 16S rRNA sequence is different from other known species.','Debnath et al. 2017',NULL,0,0),(1189,1225,'diagnosis','In nature, LBK isolate grown in alluvial rice field soil (affected by arsenic) in LGP of West Bengal, India. The trichomes are light blue green, microscopic; in solid culture plate blue green spreading colonies (Fig. 2A) and in liquid medium they appeared as blue green biomass with glass wall attachment later free, when older becoming yellowish green. Filaments are flexuous and entangled. Cells are less constricted with translucent cross walls (Fig. 2B). Sheath facultative, colourless, transparent, firm and attached to the trichome (Figs. 2B, C). Cells are cylindrical, 1.5–2.56 μm long and 0.7 to 0.97 (≤1) μm wide (Figs. 2D, E). Terminal cells subobtuse to obtuse (Figs. 2D, E). Centroplasma and chromatoplasma clearly distinguishable in centre and periphery towards the cell wall (Fig. 2F).','Debnath et al. 2017',NULL,0,0),(1190,1226,'diagnosis','Trichomes solitary, straight filaments; vegetative cells barrel-shaped to spherical, 5.1-11.5 μm wide and 5.0-10.1 μm length, length : width (L : W) ratio 0.5-1.8, with gas vesicles. Heterocytes round, colorless or light green. Akinetes light green, thin cylindrical, narrower towards the ends than at the center, 10.9-15.8 μm wide and 19.7-51.9 μm length, L : W ratio 1.7-3.8, separate from heterocytes.','Choi et al. 2018',NULL,0,0),(1191,1030,'description','Filamentous cyanobacteria, forming green, greenbrown and black compact subaerophytic biofilms on solid substrata. Filaments fine, long, straight to wavy or coiled. Sheaths thin, firm, colourless, attached to the trichomes, sometimes widened at the ends. Trichomes cylindrical, not constricted at cross walls, sometimes slightly constricted toward the end. Cells isodiametric, slightly shorter than wide or longer than wide with green or blue-green content. No heterocytes or akinetes. Plectonematoid false branching may or may not occur, and is usually due to the presence of necridic cells. Reproduction occurs via formation of hormogonia, produced by fragmentation of trichomes, often by means of irregular necridic cells.','Zammit 2018',NULL,0,0),(1192,1031,'description','Filaments with a single trichome per sheath, with or without occasional false branching. Sheath colourless, firm, thin, often open at the ends. Trichomes occasionally slightly attenuated toward their ends. Trichome fragmentation via the random occurrence of necridic cells within a filament. Cells variable in shape, mostly isodiametric, sometimes slightly shorter or longer than wide. Cell size 2–4 um long, 2–3 um wide. Cell contents homogenous, may occasionally appear grainy. Necridic cells sometimes present. Apical cell rounded. Hormogonia straight, made up of two to eight cells. Filaments grow preferentially in dimly lit areas.','Zammit 2018',NULL,0,0),(1193,1227,'description','Trichomes solitary, short, irregularly arcuated, (1)2-4(8)-celled, with very fine and indistinct diffuse slime, slightly constricted at cross-walls. Cells cylindrical, 3-6 x 0.8-1.2 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1194,1228,'description','Trichomes solitary or few in mucilaginous colourless colonies, (1)-4-celled, constricted et cross-walls. Cells 1.5-3 x 0.7-0.8 μm, pale greyish blue-green.','Komárek 2001',NULL,0,0),(1195,1228,'eco_distro','Metaphytic in small clear streams; Czech Republic (Beskydy Mts.), Italy.','Komárek 2001',NULL,0,0),(1196,1229,'description','Trichomes in small mucilaginous clusters, (1)2-4(8)-celled, clearly constricted et cross-walls, arcuated. Cells 3.7-8.3 x 0.6-0.8 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1197,1229,'eco_distro','Planktic in oxidation pond; USA (Alaska).','Komárek 2001',NULL,0,0),(1198,1230,'other','Trichomes disintegrating (numerous solitary cells in population), irregularly coiled, solitary in diffuse, indistinct slime, 1-4(12)-celled, constricted et cross-walls. Cells 1-12.8 x 0.7-1 μm, pale greyish blue-green.','Komárek 2001',NULL,0,0),(1199,1230,'eco_distro','Planktic in meso- to eutrophic reservoirs; tropical, Brazil (state Pernambuco).','Komárek 2001',NULL,0,0),(1200,1231,'description','Trichomes solitary, arcuated, very short (“few-celled”), not constricted et cross-walls, but disintegrating and composed from few segments with constrictions, mucilage?. Cells 1.5-2.5 x ± 1μm, yellow-green.','Komárek 2001',NULL,0,0),(1201,1231,'eco_distro','Benthic, epipelic in lakes with muddy bottom; Czech Republic, Denmark, northern Germany.','Komárek 2001',NULL,0,0),(1202,1232,'description','Trichomes irregularly wavy, solitary, with numerous cells, but disintegrating, with wide mucilaginous envelopes, constricted at cross-walls. Cells short, cylindrical, 1-1.5 x ± 1μm, yellow-green or pale blue-green.','Komárek 2001',NULL,0,0),(1203,1232,'other','Planktic in eutrophic ponds; Slovakia.','Komárek 2001',NULL,0,0),(1204,1233,'description','Trichomes very short, arcuated, 2-3-celled, more in gelatinous mass, constricted at cross-walls. Cells long cylindrical, ± 6 x 1 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1205,1233,'eco_distro','Subaerophytic, epiphytic on wet mosses; tropical species, Costa Rica.','Komáreka 2001',NULL,0,0),(1206,1227,'eco_distro','Planktic in ponds and lakes; known mainly from central Europe, probably over the whole temperate zones.','Komárek 2001',NULL,0,0),(1207,1234,'description','Trichomes solitary, irregularly wavy to coiled, 2-18-celled, with very fine, colourless, mucilaginous envelopes, constricted at cross-walls. Cells short cylindrical to almost barrel-shaped, 3.5-4.6 x 1.2-1.5 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1208,1234,'eco_distro','Planktic in ponds and lakes; cosmopolitan (?).','Komárek 2001',NULL,0,0),(1209,1235,'description','Trichomes solitary, very irregularly coiled, 12-24-celled, with mucilaginous, diffuse envelopes, constricted at cross-walls. Cells long cylindrical, 4.5-9.2 x 1-1.3 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1210,1235,'eco_distro','Planktic in small eutrophic ponds and pools; tropical species (?), Brazil (São Paulo state).','Komárek 2001',NULL,0,0),(1211,1236,'description','Trichomes solitary, almost straight or slightly arcuated, 8-16-celled, with mucilaginous envelopes, not constricted at cross-walls. Cells cylindrical, 1-3 x 1-1.5 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1212,1236,'eco_distro','Kryosestic; Poland (High Tatra Mts.).','Komárek 2001',NULL,0,0),(1213,1237,'description','Trichomes solitary, slightly wavy to almost straight, 4-16-celled, constricted at cross-walls. Cells cylindrical, 4-12 x ± 1.2-1.6 μm, pale blue-green; sometimes Y-formed cells occur.','Komárek 2001',NULL,0,0),(1214,1237,'eco_distro','Planktic in eutrophic village ponds; Slovakia.','Komárek 2001',NULL,0,0),(1215,1238,'description','Trichomes solitary, wavy to coiled, (1)2-18-celled, but sometimes with numerous cells (up to &gt; 60), slightly constricted at cross-walls. Cells cylindrical, 4.5-9(13) x ± 1.5 μm, pale greyish blue-green.','Komárek 2001',NULL,0,0),(1216,1238,'eco_distro','Planktic in lakes and large reservoirs; tropical species – central, east and southern Africa.','Komárek 2001',NULL,0,0),(1217,1239,'description','Trichomes solitary, always irregularly wavy, 2-12-celled, with diffuse, colourless mucilaginous envelopes, slightly constricted at cross-walls. Cells cylindrical, (2.5?)3-9 x (1?)1.3-2 μm, pale glue-green.','Komárek 2001',NULL,0,0),(1218,1239,'eco_distro','Planktic in ponds, lakes and rivers; known mainly from temperate Eurasia, but recorded also from India; cosmopolitan (?).','Komárek 2001',NULL,0,0),(1219,1240,'description','Trichomes solitary, irregularly wavy to coiled, facultatively with very diffuse and indistinct slime, usually with up to 12, rarely with numerous cells, constricted at cross-walls, usually heterocellular. Cells cylindrical, (3.5)4-14 x ± 2 μm, pale greyish blue-green.','Komárek 2001',NULL,0,0),(1220,1240,'eco_distro','Kryosestic; coastal Antarctica, Japan, USA (mountains).','Komárek 2001',NULL,0,0),(1221,1241,'description','Trichomes solitary, almost straight to slightly wavy, with indistinct mucilaginous envelopes, 2-23-celled, constricted at cross-walls, heterocellular. Cells cylindrical, 2.6-8.2 x (1.4)2.2-2.8 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1222,1241,'eco_distro','Planktic and metaphytic in large reservoirs; tropical species, Brazil (São Paulo state).','Komárek 2001',NULL,0,0),(1223,1242,'description','Trichomes solitary, short, almost straight or arcuated, usually 6-celled, not constricted at cross-walls, cylindrical, to 10 μm long, with diffuse slime envelopes. Cells ± isodiametric or shorter (!) than wide, ± 2.3 μm wide, pale blue-green.','Komárek 2001',NULL,0,0),(1224,1242,'eco_distro','Benthic in shallow lakes; eastern Austria.','Komárek 2001',NULL,0,0),(1225,1243,'description','Trichomes solitary, slightly wavy, with narrow, indistinct mucilaginous envelopes, 2-4(12)-celled, constricted at cross-walls. Cells cylindrical to sausage-shaped, 3-5(7) x (2)2.5-2.8 μm, greyish to pale blue-green; Y-shaped cells occur.','Komárek 2001',NULL,0,0),(1226,1243,'eco_distro','In summer plankton of fishponds; Slovakia.','Komárek 2001',NULL,0,0),(1227,1244,'description','Trichomes solitary, irregularly to almost regularly screw-like coiled, with diffuse mucilaginous envelopes, up to 27-celled, constricted at cross-walls. Cells cylindrical, arcuated, 5.2-12 x 2-3 μm, pale blue-green.','Komárek 2001',NULL,0,0),(1228,1244,'eco_distro','Planktic in eutrophic ponds, reservoirs and large rivers; Czech Republic, Hungary, Russia, Slovakia, Ukraine.','Komárek 2001',NULL,0,0),(1229,1245,'description','Trichomes solitary, slightly wavy, 2-8-celled (sometimes with more cells?), constricted at cross-walls, heterocellular, sometimes attached by one end to floating microscopic particles. Cells long cylindrical, 8-48(80!) x 2-3 μm, pale greyish blue-green.','Komárek 2001',NULL,0,0),(1230,1245,'eco_distro','Marine, planktic; Gulf of Mexico.','Komárek 2001',NULL,0,0),(1231,1247,'description','Trichomes solitary, seldom in fine mats, variable in length, usually from 50 to 800 μm, without visible sheaths, but amorphous slime can occur, trichomes straight or bent, 7–12 μm wide, motile (gliding) and/or seldom immotile, vegetative cells spherical, hemispherical, barrel-shaped or slightly cylindrical; all cells with four small surface holes located diagonally in the cell corners (Nomarski differential contrast); apical cells usually longer than wide, broadly conical, sometimes with a conical protrusion; cell content homogenous or with scattered granules, visible peripheral chromatoplasm, trichomes divide into short parts by breakage (hormogonia or hormocytes), no necridic disks observed. Under laboratory conditions trichomes quickly disintegrate into few- or one-celled fragments (Figs 15, 23), followed by subsequent disappearance on both solid and liquid media over several days.','Hašler &amp; Poulíčková 2001',NULL,0,0),(1232,497,'description','Filaments with multiple trichomes per sheath. Sheath colorless, unlamellated. Trichomes slightly constricted at the crosswalls, nontapering, with phormidiacean cell division. Cells with radial or fasciculated thylakoid arrangement. End cells rounded to conically rounded, noncalyptrate, typically longer than wide. Genome containing at least one ribosomal operon in which the 16S–23S ITS has genes for both tRNAIle and tRNAAla. Habitat brackish to marine, nonterrestrial.','Siegesmund et al. 2008',NULL,0,0),(1233,498,'description','Trichomes slightly constricted at the cross walls (Fig. 1, a–l) with one to many trichomes in a common sheath (Fig. 1, d and h), with limited gliding motility, tapering only at the terminal cell, lacking necridia, 2–5.5 lm wide. Cells longer than wide, blue-green to dirty blue-green, minutely granular in the centroplasm, with phormidiaceaen-type cell division, thylakoids not visible or appearing fasciculated, 4–14 lm long. Apical cell bluntly rounded after trichome breakage (Fig.1, f–h, k), becoming elongated and conical, not capitate, without calyptra.','Siegesmund et al. 2008',NULL,0,0),(1234,1061,'diagnosis','Genetically most similar to Scytolyngbya, from which it differs in the coloration and width in the sheath material and in the presence of coiled filaments. Morphologically similar to Chamaethrix, from which it differs by the obligately blackish coloration of the sheaths. It also differs notably in the secondary structure of the conserved domains of the 16S-23S ITS region and is phylogenetically distinct based on 16S rRNA gene sequence.','Becerra-Absalón et al. 2018',NULL,0,0),(1235,1061,'description','Solitary or intricated filaments, entangled with other filamentous cyanobacterial species forming biocrusts or biofilms on soil surfaces. In culture on agar-solidified media, filaments forming thin and compact biofilms, intricated, sometimes coiled, with rare single false branching. Sheaths firm, firstly thin and colorless, soon becoming thick and colored, open at the end, with one trichome per sheath. Trichomes isopolar, fine, cylindrical, sometimes tapering at ends, straight or coiled, constricted at the crosswalls. Cells isodiametric or longer than wide, with homogenous content, without aerotopes, with rare granules, pale blue-green. Apical cell conical or rounded. Reproduction by hormogonia, produced both by simple fragmentation and through formation of necridial cells.','Becerra-Absalón et al. 2018',NULL,0,0),(1236,1062,'description','Solitary or intricated filaments entangled with other filamentous cyanobacteria species forming biocrust. In culture the thallus is a thin and compact biofilm. Filaments intricated, sometimes coiled, 2.1–5.8 μm wide, with rare single false branching, with hormogonia often developing from the false branches that break but remain attached by sheath material to the parent filament. Sheaths firm, firstly thin and colorless, soon becoming thick, blackish, opaque, obscuring the trichome, open at the ends, with one trichome per sheath. Trichomes isopolar, fine, cylindrical, sometimes tapering at ends, constricted at cross walls, 1–3.8 μm wide. Cells distinctly longer than wide, sometimes isodiametric, pale blue-green, with homogenous content, lacking aerotopes, rarely granulated, 1.6–6.9 μm long. Apical cell conical, sometimes rounded. Reproduction by hormogonia, produced both by simple fragmentation and through formation of necridial cells.','Becerra-Absalón et al. 2018',NULL,0,0),(1237,1063,'description','Solitary or intricated filaments entangled with other filamentous cyanobacteria species forming biocrust. In culture the thallus is a thin and compact biofilm. Filaments intricated, sometimes coiled, 2.7–5.7 μm wide, with rare single false branching, with hormogonia often developing from the false branches that break but remain attached by sheath material to the parent filament. Sheaths firm, firstly thin and colorless, later thick, blackish, but translucent, frequently open at the ends, with one trichome per sheath. Trichomes isopolar, fine, cylindrical, constricted at cross walls, 1–3.2 μm wide. Cells distinctly longer than wide, sometimes isodiametric, pale blue-green, with homogenous content, lacking aerotopes, rarely granulated, 1.8–4.4 μm long. Apical cell cylindrical and rounded, sometimes obtusely conical. Reproduction by hormogonia, produced both by simple fragmentation and through formation of necridial cells.','Becerra-Absalón et al. 2018',NULL,0,0),(1238,1248,'description','Mats attached to the substrate. Filaments densely entangled, trichome motility present. Sheaths facultative, firm, thin, colorless, hyaline. Trichomes isopolar, cylindrical along their whole length, not constricted or constricted at the cross walls, not attenuated toward the apex, 4.8–8 um wide. Cells isodiametric or shorter or longer than wide. Cell content finely granular or with scattered larger granules. Apical cell rounded or conical-rounded, without calyptra, with thickened cell wall. Heterocytes and akinetes absent. Reproduction by disintegration of trichomes into hormogonia.','Martins et al. 2019',NULL,0,0),(1239,1249,'description','Thallus dark blue-green. Filaments entangled, 5.5–8 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, slightly constricted at the ungranulated cross walls, 4.8–7.2 um wide. Cells cylindrical, shorter to longer than wide, 3.2–7.2 um long. Cell content blue-green, homogeneous, one<br>or several terminal cells usually pale. Apical cells conical-rounded, with thickened cell wall, 4.8–7.2 um wide, 3.6–7.2 um long.','Martins et al. 2019',NULL,0,0),(1240,1250,'description','Thallus dark blue-green. Filaments entangled, 7–8 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, slightly constricted at the ungranulated cross walls, 6.5–7.5 um wide. Cells cylindrical, shorter to longer than wide, 4–7.5 um long. Cell content blue-green, homogeneous. Apical cells slightly conical-rounded, with thickened cell wall, 6.5–7.5 um wide, 4.5–7.2 um long.','Martins et al. 2019',NULL,0,0),(1241,1251,'description','Thallus dark blue-green. Filaments entangled, 7.2–8.8 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, not or slightly constricted at the ungranulated cross walls, 6.4–7.6 um wide. Cells cylindrical, shorter to longer than wide, 4–9.6 um long. Cell content blue-green, homogeneous. Apical cells conical-rounded, with thickened cell wall, 6.4–7.6 um wide, 4.8–9.2 um long.','Martins et al. 2019',NULL,0,0),(1242,1252,'description','Thallus dark blue-green. Filaments entangled, 7.2–9.2 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, not to slightly constricted at the ungranulated cross walls, 6.4–8 um wide. Cells cylindrical, shorter to longer than wide, 4–10.4 um long. Cell content brown-reddish, keritomized chromatoplasm. Apical cells rounded, with thickened cell wall, 6.4–8 um wide, 6.2–10.4 um long.','Martins et al. 2019',NULL,0,0),(1243,1253,'description','Thallus dark blue-green. Filaments entangled, 6–8.8 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, constricted at the granulated or ungranulated cross walls, 6–8 um wide. Cells cylindrical, shorter to longer than wide, 3.2–9.6 um long. Cell content brown-reddish, granulated. Apical cells rounded, with thickened cell wall, 5.6–8 um wide, 5.6–8.4 um long.','Martins et al. 2019',NULL,0,0),(1244,1254,'description','Filaments entangled, 5–7 um wide. Sheaths firm, thin, homogenous, colorless. Trichomes motile, cylindrical, not attenuated, not slightly constricted at the ungranulated cross walls, 4–7 um wide. Cells cylindrical, shorter to longer than wide, 3.5–8 um long. Cell content blue-green, homogeneous. Apical cells rounded, with thickened cell wall, 4–7 um wide, 5.5–8 um long.','Martins et al. 2019',NULL,0,0),(1245,612,'description','Trichomes straight, motile (trembling) with 4–8 or many cells. Trichomes typically 20–46 um, but up to 229 um long in culture. Cells mostly blue-green, with scattered granules, usually long cylindrical or barrel-shaped when starting division, 1.5-3.5 um wide and 6.3-12.0 um long. Terminal cells flattened or slightly conical. Necridic cells, akinetes, aerotopes and heterocytes not observed.','Nguyen et al. 2013',NULL,0,0),(1246,1087,'description','Thalli vary in shape from amorphic feathery, undulating or wispy to puffball-shaped clumps, often forming thick, undulating, digital projections; specimens up to 20 cm long; basal parts composed of empty polysaccharide sheaths, colorless or whitish, and mucilaginous; exterior composed of living, pigmented, filaments that vary in coloration such as red, orange, and green; filaments unbranched with individual sheaths, typically entangled into fasciculated bundles; filaments (4) 5–6 (7) um in diameter; trichomes cylindrical, surrounded by thin (&gt;0.5 um), barely visible, polysaccharide sheaths; cells barrel-shaped or cylindrical (4) 5–6 (7) um broad and (5) 6–8 (10) um long, with no constrictions at cross-walls; terminal cells of filaments rounded; trichomes lack heterocysts or other specialized cells; producing secondary metabolites dolastatin 10 and/or symplostatin 1, and sometimes largazole.','Engene et al. 2015',NULL,0,0),(1247,1086,'diagnosis','Thalli habit from amorphic feathery or wispy to puffball clumps, sometimes mat-like. Coloration varies from red to orange and green. Each filament composed of entangled, thin, unbranched filaments; trichomes cylindrical, lacking heterocysts, and other specialized cells, surrounded by barely visible polysaccharide sheaths. Cells barrel-shaped or sometimes cylindrical.&nbsp;','Engene et al. 2015',NULL,0,0),(1248,1129,'description','Thallus forming extensive fasciculate mats or small clusters, brown, brown-green, olive-green to darkgreen, dark blue-green to black. Filaments straight, isopolar, unbranched, (8-) 12-30 (-46) μm diam. Sheaths hyaline or bright yellow to yellow-brown, firm, thin or thick, sometimes lamellated. Trichomes not or slightly constricted at the cross-walls, not or slightly attenuated towards ends, (6.6-) 10-21 (-24) μm diam., sometimes some trichomes become contorted to originate the necridial regions. Cells 1.4-5.6 (-6) μm long, 1.2-11 times wider than long. Cross-walls often granulated, sometimes with large granules. Apical cells rounded, conical, conicalrounded, flat-rounded, truncate, rarely capitate, sometimes thickened, without calyptra. Hormogonia formed by fragmentation perpendicular to the longitudinal axis of the trichome helped by necridic cells, or in diagonal position, in this case helped or not by necridic cells.','Caires et al. 2018',NULL,0,0),(1249,1130,'description','Thallus fasciculate, forming extensive mats, brown. Filaments straight, 14-16.4 μm diam. Sheaths hyaline, thin or slight thick, firm. Trichomes cylindrical, slightly constricted at the cross-walls, and sometimes slightly attenuated towards ends, 12.1-14.6 μm diam. Discoid cells, 1.7-2.5 μm long, 5.8-7 times wider than long. Cell content dark-green, granulated. Crosswalls granulated, sometimes with large granules. Apical cells rounded, conical-rounded, conical, flat-rounded, without thickening. Hormogonia formed by cross-wise diagonal fragmentation of the trichome, helped or not by necridic cells.&nbsp;<br><strong>Ultrastructural notes:</strong> Thylakoidal membranes presented parietal or irregular arrangement, which are distributed in different regions of the cell; cyanophycin granules occurred frequently near the cross-walls. Gas<br>vesicles were observed usually in the inter-thylakoid space, frequently forming irregular clusters (aerotopes)<br>near the cell wall and cross-wall.','Caires et al. 2018',NULL,0,0),(1250,1131,'description','Thallus fasciculate, forming small clusters, black. Filaments straight, 12-15.8 μm diam. Sheaths hyaline, thick, firm, frequently lamellated. Trichomes slightly constricted at the cross-walls, 10.1-12.9 μm diam., someone occasionally becomes contorted to originate the necridial regions. Cells 1.4-2.1 μm long, 1.2 times wider than long. Cell content green, sometimes granulated, and with numerous gas vesicles. Cross-walls granulated. Apical cell rounded or conicalrounded, rarely capitate. Hormogonia formed by straight fragmentation helped by necridic cells, or in diagonal position, in this case helped or not by necridic cells.&nbsp;<br><strong>Ultrastructural notes: </strong>This species presented thylakoidal membranes with irregular arrangement and numerous gas vesicles occurring in great number near both cross and cell walls.','Caires et al. 2018',NULL,0,0),(1251,118,'molecular','','Fiore et al. 2007','[193]',0,0),(1252,667,'description','Filaments solitary or in irregular clusters, colonies sometimes densely and ± parallel entangled and forming flat or hemispherical mats on substrates, cylindrical, more or less slightly coiled, sometimes joined in irregular parallel formation, with facultative sheaths (usually present). Developed sheaths are firm, firstly thin, colorless, slightly yellowish-brown or black, in old cultures thick, lamellate, sometimes mucilaginous, containing one, rarely 2–3 trichomes. Trichomes cylindrical, usually distinctly constricted at the cross-walls, not attenuated towards ends, without diversified terminal cells, necridic cells present. False pseudobranching and distinct nodi are occasionally present. Cells isodiametric, slightly shorter or longer than wide, with central granules. Cells are usually rounded from the sides, with parietally arranged thylakoids, sometimes with small irregularities. Terminal cells are rounded without calyptra.','Raabová et al. 2019',NULL,0,0),(1253,1282,'description','Filaments straight or slightly curved, solitary or entangled, with one or two trichomes per sheath. Filaments pale blue-green, constricted at the cross-walls. Sheath colorless, thick, sometimes narrowed towards the ends, mucilaginous. Filaments 1–2.5(3) μm wide. Cells are 1–3(3.5) μm long. Cells are barrel-shaped or shorter than wide, occasionally longer than wide. Central granules are present in cells. Nodi are rarely present on filaments in old cultures, or they are falsely pseudobranched. Apical cells are rounded without calyptra.','Raabová et al. 2019',NULL,0,0),(1254,1282,'eco_distro','Subaerophytic in soil crusts, on bones and in epilithon in lakes; probably distributed worldwide.','Raabová et al. 2019',NULL,0,0),(1255,1283,'description','Filaments straight or curved, solitary or irregularly arranged in clusters, or entangled, with one or more trichomes per sheath. Filaments pale blue-green, dark olive-green to yellow-brown. Filaments slightly constricted at the cross-walls. Sheaths are invisible in young cultures or thin, colorless, in old cultures getting thicker, colorless or brownish when exposed to strong light, sometimes lamellate. Filaments 1.5–3(4) μm wide. Cell length is 1–3(5) μm. Cells are barrel-shaped or shorter than wide, occasionally longer than wide. Central granules are characteristic. Specific nodi are present on filaments in old cultures, or scarcely falsely pseudobranched. Apical cells are rounded, without calyptra.','Raabová et al. 2019',NULL,0,0),(1256,1284,'description','Filaments long, straight or curved, solitary or sometimes in ± irregular clusters with more filaments per sheaths. Filaments sometimes entangled. Sheaths thick in young cultures, colorless or grey. In old cultures sheaths firm, lamellate, violet or blackish, sometimes open at the end. Filaments slightly constricted at the end, occasionally with necridic cells. Distinct nodi sometimes occur on filaments in old cultures. Cells are barrel-shaped. Central granules are present in center of cells. Filaments are 1.5–2.5(4) μm wide and 1–2(3.8) μm long. Apical cells are rounded, without calyptra.','Raabová et al. 2019',NULL,0,0),(1257,1284,'eco_distro','Wet rocks, surface of bones, cave walls; very similar strains are known from the littoral of lakes and from thermal springs; deglaciated areas in the Arctic, Antarctica, in Greece (caves), probably distributed worldwide.','Raabová et al. 2019',NULL,0,0),(1258,1285,'description','Filaments straight, curved, flexuose or wavy, solitary, one filament per sheath. Filaments pale bluegreen to dark green. Filaments slightly constricted at cross-walls, slightly wider on the apical part of filament. Sheaths are thick, colorless. Cells barrel shaped and with central granules in cells. Apical cell is rounded without calyptra. Morphology of filaments change during the life cycle. The morphology of young filaments similar to <em>Leptolyngbya corticola</em> or<em> L. boryana </em>(Gomont) Anagnostidis &amp; Komárek (1988: 391), but when older similar to <em>Phormidesmis</em>.','Raabová et al. 2019',NULL,0,0),(1259,1286,'description','Filaments straight, curved, flexuose or wavy, solitary, one filament per sheath. Filaments pale bluegreen to dark green, slightly constricted at cross-walls. Sheaths thick, colorless. Filaments 2.5–3.5(4) μm wide, occasionally with necridic cells. Cell length 1–2 μm. Cells barrel shaped or shorter than wide, occasionally longer than wide with central granules in cells. Apical cell is rounded without calyptra.','Raabová et al. 2019',NULL,0,0),(1260,1286,'eco_distro','Antarctica, South Shetlands, caldera Deception Island, mud of littoral pools','Raabová et al. 2019',NULL,0,0),(1261,1287,'description','filamentous cyanobacteria that often form entangled masses to extensive mats; filaments unbranched, straight or curved, and up to a few centimeters in length; trichomes cylindrical, not attenuated toward the end, not constricted to slightly constricted at cellular cross walls, and enclosed by thin yet clearly visible polysaccharide sheaths; cells always discoid, shorter than wider; terminal cells of the filaments rounded and sometimes slightly elongated; heterocysts or other specialized cells absent.','Engene et al. 2018',NULL,0,0),(1262,1288,'description','growth form ranges from small tufts to large mats and extensive blooms; filaments darkblackish, unbranched, straight or slightly waved, up to several centimeters in length, and ranging between (27) 32–35 (40) um in diameter; trichomes cylindrical, not attenuated towards the end, not constricted to slightly constricted at cellular cross walls, and surrounded by thin (0.5 um) polysaccharide sheaths; cells always discoid, shorter than wide, (28)30–34 (40) um wide, and (1) 2–3 (4) um long; terminal cells of the filaments rounded or cupuliform; filaments lack heterocysts or other specialized cells, but contain nitrogen-fixing genes; multiple cyanophycin granules per cell, thylakoid membranes positioned close to and perpendicular to cross walls; bundles of gas vesicles; produces the bioactive secondary metabolite malyngolide','Engene et al. 2018',NULL,0,0),(1263,1289,'description','thin red or red-brownish mats and extensive blooms; filaments dark red, unbranched, straight or curved, up to a few centimeters in length, and ranging between (22) 26–29 (39) um in diameter; trichomes cylindrical, not attenuated toward the end, not constricted to slightly constricted at cellular cross walls, and enclosed by thin polysaccharide sheaths; cells always discoid, shorter than wide, (22) 24–26 (34) um wide, and (1) 3–4 (5) um long; terminal cells of the filaments rounded and sometimes slightly elongated; lack of heterocysts or other specialized cells, but contain nitrogen-fixing genes; produces lyngbic acid','Engene et al. 2018',NULL,0,0),(1264,1290,'description','Thallus flat, thin, spreading diffusely from the center, penetrating into the agar, blue-green. Filaments flexuous,(1.5)1.9–2.5(3.0) μm wide, mostly unbranched. Sheath very common, nearly obligate in older cultures, thin and tightly attached when young, later distinctly widened, colorless. Trichomes motile only in young state, olivegreen, (1.3)1.7–2.3(2.7) μm wide, clearly constricted at cross walls (especially in young cultures) and sometimes with granules, lacking necridia, not attenuated to the end. Cells isodiametric to longer than wide, (1.3)1.7–3.7(4.7) μm, with nongranular cytoplasm and parietal thylakoids clearly visible in the light microscope. Mature apical cells bluntly conical, longer than vegetative cells, 1.3–1.7(2.3) μm wide, (2.3)3.3–6.7 (7.7) μm long, with a reddish-orange spot in the apex of the cell. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix with only 8 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix with 52 nucleotides, with a unilateral bulge on the 5′ side of the helix.','Vinogradova et al. 2017',NULL,0,0),(1265,1291,'diagnosis','Morphologically and phylogenetically it is the most similar to <em>O. hafneriensis</em> and <em>O. neakameniensis</em>, from which differs in higher degree of sheath formation, false branching, granulations at cross walls and longer intercalary cells, and by composition and secondary structure of 16S-23S ITS region.','Vinogradova et al. 2017',NULL,0,0),(1266,1291,'description','Thallus a thin film penetrating into the agar, spreading diffusely from the center of thallus, bluegreen. Filaments weakly waved, rarely with false branching or more than one trichome in common sheath. Sheath nearly obligate, first thin and tightly attached, (1.3)1.5–1.9 μm wide, in old cultures firm, gradually expanded, sometimes &nbsp;lamellate, 5–7.5 μm wide, colorless. Trichomes olive-green, (1.1)1.3–1.7 μm wide, unconstricted to slightly constricted at the cross walls (especially in young cultures) often flanking with granules, lacking necridia, not attenuated to the end. Cells consistently longer than wide, with nongranular cytoplasm, with parietal thylakoids clearly visible in the light microscope, (2)2.3–4.7(5) μm long, in old cultures up to 7.5 μm long. Mature apical cells elongated-conical, longer than vegetative cells, 1.3–1.5 μm wide, (4.0)5.0–7.0(8.7) μm long, with a reddishorange spot in the apex of the cell. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix 15 nucleotides long, with a terminal loop of 7 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix region with 53 nucleotides, with a unilateral bulge on the 5′ side of the helix at nucleotides.','Vinogradova et al. 2017',NULL,0,0),(1267,1114,'description','Triehomes 7-9um diam., forming an open regular spiral of 3-8 turns 40-60um diam., 70-80um between the turns, slightly tapering at the ends; cells 5-7um long, not constricted, with numerous, coarse, angular, refringent granules frequently crowded at the partitions; end walls of the terminal cells rounded, slightly thickened; color verdigris.','Gardner 1917',NULL,0,0),(1268,1114,'eco_distro','Floating in abundance among other species of Cyanophyceae in warm salt water. Key Route Power-house, Oakland, California, July, 1916.','Gardner 1917',NULL,0,0),(1269,482,'description','Colony tough, mounded in the agar, red-brown. Filaments short, 1–1.7 µm in width. Sheath absent or thin, colorless, tightly adhering to trichomes, visible only when empty. Trichomes short, untapered, unconstricted at the crosswalls, sometimes coiling, 0.8–1.2 µm wide. Cells longer than wide, with parietal thylakoids, with claret-colored, nongranular cytoplasm, 2.8–4.8 µm long.','Miscoe et al. 2016',NULL,0,0),(1270,1296,'description','Cells aggregated into microscopic masses, indefinite in shape and size, not forming a definite stratum, short, cylindrical, 0,8-1 um diameter, about 2 times as long as the diameter.','Gardner 1927',NULL,0,0),(1271,477,'description','Colonies macroscopic, forming irregular mass­es of minute mucilaginous spheres on the rock substrate, pinkish purple on both native substrate and agar. Mucilage clear, diffluent. Cells lacking individual sheaths, mostly solitary, but also in pairs, rarely in tetrads showing division in two planes, spherical, lilac in color, 0.8–1.6 µm in diameter. Cytoplasm homogenous or with 1–2 granules per cell.','Miscoe et al. 2016',NULL,0,0),(1272,476,'description','Colonies diffuse, dark green to black on the agar, composed of tightly arranged cells, at first in radially arranged colonies or cubical colonies, later forming rounded three dimensional aggregates, 10–28 µm in diameter. Mucilage diffluent, not forming any firm sheaths. Cells bright blue-green, becoming dark blue-green or grey, with clear demarcation of centroplasm and parietal thylakoids, with nongranular cytoplasm, dividing by binary fission, spherical, subspherical, oval, or irregularly shaped, constricted bacilli immediately prior to or during division, solitary, in pairs, or in aggregates of 4, 8 or numerous cells, 2.5–4.3 µm in diameter.&nbsp;','Miscoe et al. 2016',NULL,0,0),(1273,445,'description','Filaments unbranched. Sheath colorless, often absent. Trichomes constricted at the crosswalls, lacking necridia, mostly with rounded end cells. &nbsp;Cells longer than wide, with parietal thylakoids.','Miscoe et al. 2016',NULL,0,0),(1274,475,'description','Colony a spreading mat, penetrating the agar, dark purplish brown. Filaments lacking pseudobranching, sometimes with a widened sheath containing one to two coiled trichomes, up to 3.2 µm wide. Sheath thin, colorless. Trichomes untapered, slightly to distinctly constricted at the crosswalls, 1.5–1.7 µm wide. Cells mostly a little longer than wide, grayish green to purplish brown in color, homogenous with parietal thylakoids, 1.0–2.0 µm long. End cells rounded with no granules present.','Miscoe et al. 2016',NULL,0,0),(1275,480,'description','Colonies green, penetrating into the agar. Filaments consisting of a single trichome, sometimes coiled, with or without a sheath, 1.2–1.7 µm wide. Sheath, thin, colorless, evident only when trichome is absent. Trichomes untapered, unconstricted at crosswalls, 0.9–1.2 µm wide. Cells green in color, longer than wide, 2.4–3.2 µm long. Apical cells elongated, conical, some with red inclusions at the apices, 1.8–7.8 µm long, 0.9–1.4 µm wide.','Miscoe et al. 2016',NULL,0,1),(1276,478,'description','Filamentous cyanobacteria, forming reddish, sometimes greenish compact subaerophytic biofilms on solid calcareous substrata. Filaments fine, long, coiled into clusters and wavy, ensheathed and mostly unbranched. Sheaths colourless, thin, firm, enveloping one trichome and usually attached to it or slightly distant, occasionally open at the ends. Trichomes fine (1–3 um wide) and cylindrical, slightly constricted at cross walls, not attenuated toward the ends. False branching occurs very rarely under culture conditions. Cells cylindrical, longer than wide, with homogeneous content, no aerotopes, rare presence of granules. Apical cell conical-rounded, with an orange spot at the tip. No heterocytes or akinetes. Cells divide by symmetrical crosswise binary fission. Reproduction via formation of hormogonia, produced by fragmentation of trichomes, mostly without the formation of necridic cells.','Zammit et al. 2012',NULL,0,0),(1277,479,'description','Filaments generally unbranched, with a single trichome per sheath. Sheath colourless, firm, thin, often open at the ends. Trichomes cylindrical, slightly constricted at the cross walls, not attenuated towards their ends, 1–2 um wide. No necridic cells present. Trichomes appear purple-red when isolated in unicyanobacterial culture, and exhibit gliding movement and phototaxis. Vegetative cells reddish, cylindrical, 1–2 um wide, 1.5–3 um long. Cell contents homogeneous. Cells appear longer towards the middle of the trichome. Apical cell rounded with an orange structure at the tip and rhodopsin-like pigment. Hormogonia straight, made up of 2–6 cells, cells slightly longer than wide. It forms subaerophytic biofilms on illuminated calcareous substrata in subterranean sites.','Zammit et al. 2012',NULL,0,0),(1278,481,'description','Filaments without false branching, less than 2.5 µm in width. Sheath thin. Trichomes short, untapered, lacking necridia. Cells longer than wide, with parietal thylakoids. End cells cylindrical, rounded, similar to intercalary cells.','Miscoe et al. 2016',NULL,0,0),(1279,720,'description','Thallus in nature powdery and blackish, consisting of smooth dark green hemispheres when on agar. Cells either solitary or in irregular groups of up to 4 cells, mostly spherical, sarcinoid cell division into packets of four cells, rarely in very short linear series, blue-green, granulated, 2.9–6.3 µm in diameter. Cells producing baeocytes up to 30.0 µm in diameter. Baeocytes up to 32 in a single mother cell, 3–4 µm in diameter in early stages of development.','Miscoe et al. 2016',NULL,0,0),(1280,794,'description','Colonies green brown and in round tufty clumps on the agar. Filaments long, brownish purple, sometimes with double false branching. Sheath thin, colorless, tightly adhering to the cell. Filaments when young cylindrical, unconstricted, with intercalary heterocytes, with thin crosswalls, 3.6–8.9 µm wide. When mature, filaments becoming irregularly widened in the central parts of the trichome, or widened at the apices, 5.3–26.3 µm wide, sometimes with the presence of thylakoid-free cell sap. Vegetative cells with purplish-gray cytoplasm, in young filaments longer than wide, cylindrical, 2.6–10.7 µm long. In broadened parts of trichome, vegetative cells becoming disk-like, 2.0–5.4 µm long. Apical cells globose, as wide as trichomes in young filaments, becoming wider than trichomes in mature filaments. Heterocytes intercalary with two polar nodules, compressed cylindrical, shorter to longer than wide, fulvous yellow, 4.6–6.8 µm wide, 6.4–8.2 µm long.','Miscoe et al. 2016',NULL,0,0),(1281,714,'description','<strong>:<i>&nbsp;</i></strong>Colonies small, densely clumped, consisting of small clusters of coccoid cells or filaments, purplish black in color. Filaments composed of uniseriate series of globose cells, strongly contorted to give the appearance of being multiseriate, strongly constricted, 3.0–8.0 µm wide. Vegetative cells spherical, compressed globose, or irregularly obovoid, blackish, brownish violet, or dull blue-green, 2.5–8.0 µm long. &nbsp;Heterocytes clear, apical, elongated, spherical or hemispherical, with homogenous contents, 2.7–5.8 µm long, 3.6–6.1µm wide. Akinetes intercalary, apoheterocytic, in long series, with smooth, thickened wall, dull yellow-green, minutely granular, 3.3–7.5 µm long, 5.5–7.0 µm wide. Hormogonia emerging from akinetes perpendicular to the axis of the filament.','Miscoe et al. 2016',NULL,0,0),(1282,716,'description','Colonies forming golden yellow to light orange mucilaginous spheres on the agar. Filaments loosely arranged hormogonia in recently transferred cultures, forming twisted and coiled aggregates in older cultures, embedded in a soft, diffluent common mucilage. Sheath colorless, without a firm outer layer. Trichomes sinuous, 2.5–3.6 µm in width. Cells compressed globose to longer than broad, but not deeply constricted at crosswalls, yellow brown to grey, with granular cell contents, 2.0–4.0 µm long. Heterocytes colorless, intercalary, spherical to compressed, 2.5–3.5 µm long, 2.5–3.0 µm wide. Akinetes blackish green to yellowish brown, becoming wine-colored, granular, with a thin, smooth epispore, 3.0–6.7 µm long, 3.0–7.0 µm wide.','Miscoe et al. 2016',NULL,0,0),(1283,711,'description','Filaments heteropolar, clearly tapering, strongly constricted at the crosswalls. Sheath thin, barely visible. Vegetative cells isodiametric in basal portion, longer than wide near trichome apices. Heterocytes solitary, basal, hemispherical. Akinetes forming in series in basal portion of trichome.','Miscoe et al. 2016',NULL,0,0),(1284,712,'description','Colony a diffuse, light colored, spreading colony, dull grayish blue-green. Filaments heteropolar, clearly tapering, strongly constricted at the crosswalls, 4.0–6.0 µm wide at the base, tapering gradually to ends, apices 2.2–2.9 µm wide. Sheath colorless, thin, barely visible. Vegetative cells homogenous to sparsely granular, isodiametric in basal portion, longer than wide near trichome apices, 3.8–4.0 µm wide, 2.5–5.5 µm long. Heterocytes solitary, basal, hemispherical, 2.5–4.4 µm long, 3.6–4.4 µm wide. Akinetes forming in series in basal portion of trichome, homogenous to coarsely granular, 3.3–7.5 µm long, 2.5–5.7 µm wide.','Miscoe et al. 2016',NULL,0,0),(1285,717,'description','<strong><i></i></strong>Colonies blackish mucilaginous spheres or hemispheres on the agar, without a firm outer layer. Sheath colorless, diffluent. Filaments at first loosely arranged in a common mucilage, becoming more densely arranged with age, but always with trichomes apparent. Trichomes sinuous, entangled, without differentiated end cells. Cells spherical to compressed globose, slightly shorter to slightly longer than wide, grey to pale dull brown, with granulated cytoplasm, 1.8–3.0 µm wide, 1.5–3.7µm long. Heterocytes rare, clear, enlarged, spherical to ovoid, 4–6.2 µm in diameter. Akinetes with homogenous cytoplasm, mostly longer than wide, intercalary, irregularly shaped, 4–8.6 µm long, 3–5.7 µm wide.','Miscoe et al. 2016',NULL,0,0),(1286,721,'description','Filaments of main axis uniserate, lacking sheaths, densely laterally branched, strongly constricted at the crosswalls. Cells comprising the main axis rounded. Filaments of branches swollen at the base, markedly tapering to thin, unconstricted, unbranched trichomes. Cells of branch filaments rounded at base, becoming cylindrical and elongated. Heterocytes intercalary, lateral, or terminal, isodimetric to elongate-cylindrical.','Miscoe et al. 2016',NULL,0,0),(1287,722,'description','Colonies bright blue-green, with rounded tufts penetrating agar. Filaments of main axis straight, not coiled, uniserate, lacking sheaths, richly, mostly one-sided, laterally branched, strongly constricted at the crosswalls, 6-13 µm wide. Cells comprising the main axis rounded, slightly shorter to slightly longer than wide, 6-11 µm long. Filaments of branches never branching when still attached to main axis, swollen at the base, quickly tapering to 3.4-7 µm wide. Cells of branch filaments rounded at base, becoming cylindrical, up to 4 times as long as wide, 6-15 µm long. Heterocytes intercalary, lateral and terminal, 5-8 µm wide in the main axis, 7-14 µm long, typically more elongated in the branched regions 4-7 µm wide, 7-19 µm long.','Miscoe et al. 2016',NULL,0,0),(1288,723,'description','Colonies fuzzy, with upright filaments, light green on the agar, spreading in all directions from the colony center. Sheath thin, colorless, only apparent when cells are absent. Filaments heteropolar, with rare single and double false branching. Trichomes slightly to distinctly constricted at the cross walls, 7.1–16.0 µm wide. Cells blue-green, minutely granular, compressed disc-like to shorter than wide when rapidly dividing, becoming barrel-shaped to cylindrical and longer than wide in older cultures, 4.0–13.6 µm long. End cells hemispherically rounded. Heterocytes basal, one to three in a series, orange gold in color, subspherical to spherical, 9.0–13.2 µm long, 8.5–13.0 µm wide.','Miscoe et al. 2016',NULL,0,0),(1289,1304,'description','Lager dünnhäutig, lebhaft blau- bis smaragdgrün, schleimig. Fäden 1.7 bis 2.3 um dick, gekrümmt, dicht verflochten. Veget. Zellen etwas länger als dick, mit blaugrünem Inhalte. Scheiden eng, farblos.','Kützing ex Hansgirg 1892',NULL,0,0),(1290,1304,'other','Czech Republic','country',NULL,0,1),(1291,1306,'description','Stratum tenue, laete-aerugineum. Fila recta vel varie curvata, parallela. Vaginae in mucum &nbsp;amorphum diffluentes, chlorozincico jodurato caerulescentes. Trichomata pallide aeruginea, ad genicula distincte constricta, apice non attenuata. &nbsp;Cellulae quadratae vel rectangulares, 1,5-2 um latae, 1,5-4 um longae. Cellula &nbsp;apicalis subtruncata, &nbsp;calyptram par\'am &nbsp;praebens.&nbsp;','Lemmermann 1914',NULL,0,0),(1292,1311,'diagnosis','Thallus constans ex filis dense intricatis, in agarum penetrantem, obscure olivaceus. Fila trichomis singularibus, raro trichomis 2–3 arcte torsivis, interdum singulatim pseudoramosa, typice 3.4–4.0 mm lata, usque ad 6 mm ubi ultra trichomas singularem continentem. Vagina incolorata diffluens tenuis raro ultra apicem trichomatis extensa, interdum absens. Trichomata immobilia, brevissima vel usque ad ultra 200 mm longa, non decrescentia, autem interdum hormogonia angustata errerentes, divisione cellularum ut in Pseudanabaenaceis, ad septa constricta, septis saepe vix visibilis, necridiis carentibus, (2.5)3.0–3.5 mm lata. Cellulae non granulares, thylacoidibus 5–7 peripheralibus secus parietes externos et septa, centroplasmate cylindrico et distincte visibilis, quadraticae vel breviores quam latiores, 1.2–3.5 mm longae. Cellulae apicales obtusi rotundatae, non differentes quam cellulae intercalares.','Casamatta et Johansen 2015',NULL,0,0),(1293,1311,'etymology','Named for the distinctively tapering hormogonia (angustata = narrowed)','Casamatta et Johansen 2005',NULL,0,0),(1294,1313,'diagnosis','P. strato tenuissimo membrauaceo pallide aerugineo; filis flexuosis et tortuoso-intricatis; vaginis muco hyalino agglutinatis; trichomatibus angustissimis, laete aerugineis, ad dissepimenta constrictis, apicibus rectis et non capitatis cellulis diametro 2-8-plo (plerumque 4-5-plo) longioribus, protoplasmate homogeneo. Crass, trich. 0.6-0.8 um.','West et West 1897',NULL,0,0),(1295,1315,'diagnosis','Ph. filis non in strato associatis, sed inter algas varias Myxophycearum libere natantibus, brevibus; vaginis indistinctis, plerumque diffluentibus; trichomatibus brevibus vel brevissimis, pallide serugineis, valde et subirregulariter spiraliter contortis, apicibus obtusis et non attenuatis; cellulis diametro trichomatis 1-2-plo longioribus, contentu homogeneo. Crass, trich. 0.6 um; long. cell. 0.6-1.2 um','West et West 1911',NULL,0,0),(1296,1316,'diagnosis','Fila solitaria, 1.2-2.5 um lata. Vagina incolorata, tenuis, interdum absens. Trichomae constricta, non desceresentes, cellulis apicalibus, obtuse rotundis, 1.2-1.7 um latae. Cellulae nongranulatae vel granula singularia ad septa, plerumque longiores quam latae, thylacoidibus peripheralibus interdum visibilibus secus parietes externos, 1.5-4.0 um longae.','Johansen et Olsen in Johansen et al. 2008',NULL,0,0),(1297,1319,'diagnosis','Filamenra solitaria, flexuosa, &nbsp;plus minusve 1.7 um lata; vaginae tenues, firmae; trichomata cylindrica, ad dissepimenta haud constricta, ad apices haud attenuata. Cellulae plus minusve isodianetricae, aeruginosae; cellula apicalis rotundata. - Habitatio in muco algarum, praecipued <em>Batrachospermum</em>&nbsp;','Anagnostidis 2001, Preslia 73: 364',NULL,0,0),(1298,1323,'description','Filaments scattered on or within the soft tegument of the host, long and relatively straight, 0.8-1.0 um in diameter; trichome 0.7-0.9 um in diameter, not constricted at the dissepiments, neither uncinate nor capitate; cells 9-13 um long, cross walls inconspicuous, with two conspicuous granules at each cross wall, eruginous; sheath imperceptible except where there is a break in the trichome or occasionally at the ends of the trichome.','Gardner 1926',NULL,0,0),(1299,1325,'description','Stratum salmon-pink, flesh-colored or red, often mixed with other algae or poorly developed, up to 2 mm. In thickness, soft spongy to flocculent; at high temperatures filaments often free or in small clumps. Filaments packed, twisted and contorted, or for short distances straight to flexuous, with completely confluent sheaths. Sheaths thin, soft, confluent into a general homogeneous matrix, hyaline or in masses pinkish. Trichomes twisted, often crooked, rarely straight, 0.3-0.5 um in diameter, long or at high temperatures often fragile and short, not constrlcted at the cross walls. Cells 1.5-3.0 diameters in length, pale blue-green, with inconspicuous cross walls. Apices straight, not tapering; endcells rounded, unmodified.','Copeland 1936',NULL,0,0),(1300,1327,'diagnosis','Thallus macroscopicus, luteo−brunescens vel aurantiaco−brunescens, strata tenues formans cum superficie laevi. Filamenta plus−minusve recta, paucim circinata vel flexuosa, solitaria ad dense conglomerata in fasciculis irregularis, ad marginem plus minusve paralleliter fasciculatis; aliquot filamenta in fasciculis dense spiraliter circulariterque contorta. Trichoma cylindrica, pal− lide griseo−aeruginosa vel luteo−fusca, in massis aurantiaco−fusca, 1.2–2.4 μm lata, ad dissepimenta not vel rarissime paucim constricta, ad apices not attenuata. Vaginae facultativae sed distinctae, tenues, firmae, sine colore. Cellulae paucim vel clare longior quam latae (ad 2.5−plo), cellulae terminales rotundatae cum membrana externa paucim incrassata (“capitatae”).','Komárek 2007',NULL,0,0),(1301,1328,'diagnosis','Thallus macroscopicus, planus, aurantiacus vel vermiculato-lateritius, stratum supernum in coloniis crustaceis in locis humidis irriguisque formans. Filamenta dense irregulariterque intricata, vel plus minusve paralleliter ordinata praecipue in partis marginalis. Trichoma tenues, cylindracea, ad apices non attenuata, pallide griseo−aeruginosa, in massis lateritia, (0.5)0.6–1.0(1.2) μm lata, ad dissepimenta non constricta; dissepimenta vix visibilia. Vaginae tenues, incolores, saepe gelatinosae et diffluentes in massis. Cellulae plus minusve isodiametricae, vel paulo longior quam latae (ad 2–5−plo), cellula apicalis rotundata.','Komárek 2007',NULL,0,0),(1302,1329,'diagnosis','Thallusmicroscopicus; filamenta libere intricata, vel in fasciculis parvis, irregularibus, nigrescentis, mucilaginisque aggregata. Filamenta irregulariter circinata vel flexuosa, plus minusve 2.0–2.5 μm lata, ad apices leviter attenuata (vaginae). Trichoma cylindrica, pallide griseo−aeruginosa, 0.8–2.2 μm lata, ad apices not attenuata, leviter ad dissepimenta constricta. Vaginae tenues vel distinctae, postea firmae, externe levae vel paucim granulosae, spadiceae vel nigrae in medio filamentis. Cellulae plus minusve curtae, isodiametricae vel paulo longiores quam latae; cellula apicalis rotundata.','Komárek 2007',NULL,0,0),(1303,1330,'diagnosis','Filamenta solitaria vel thallus micro− vel macroscopicus, plus minusve planus, mucilagineus, griseus cum filamentis intricatis, fasciculatis, plus minusve paralleliter ordinatis. Filamenta paucim circinata vel flexuosa, recta ad apices. Trichoma cylindrica, ad apices not attenuata, pallide griseo−aeruginosa ad incolora, in massis luteo−brunescens, 1.0–2.2 μm lata, ad dissepimenta not constricta; dissepimenta vix visibilia. Vaginae tenues, sine colore, diffluentes. Cellulae paucim longiores quam latae (ad 2−plo), sine granulis; cellula apicalis interdum conice rotundata.','Komárek 2007',NULL,0,0),(1304,1333,'diagnosis','Fila badia, dense intricata, trichomis plerumque una vel raro duabus, usque ad 2.5 um lata. Vagina fulginosa, firma, laevis, aperta, fulginosa. Trichoma constricta ad septa, non descrescentes, cellulis apicalibus obtuse rotundis, 1.0-1.3 um latae. Cellulae nongranulatae, subaeruginosae, 2.0 um longae.','Johansen et Lowe in Johansen et al. 2008',NULL,0,0),(1305,1341,'diagnosis','Crustas variis Algis Myxophyceis lormatas incolens. Fila vix elongata, in glomerulos densos intricata, pressione radiantia, valde tortuosa. Homoeothricis modo utrinque attenuata et quasi pilifera, haud infrequenter pseudo-ramosa, pseudo-ramis geminatis, patentibus, saepius parallelis. Vaginae in media parte filorum crassse et aureo-fuscae, extremitates versus sensim ac sensim attenuatae et decoloratae. Trichomata dilute aeruginea, torulosa, submoniliformia, 2-2,5 um crassa, brevi-articulata; articuli diametro ad triplo breviores; cellula apicalis rotundata.','Gomont 1899',NULL,0,0),(1306,1345,'description','Stratum extended, up to 4 (rarely 5) cm in thickness; cartilaginous, homogeneous, not lamellate, deep blue-green above, pale blue-green to whitish in lower portions, surface covered with anastomoslng wrlnkles raised as much as 2 mm above the general surface. Trichomes 1.3-2.0 um in diameter; cells 3.5-6.0 um in length. Sheaths distinct in part, completely confluent i n other parts. Otherwlse as in the species.','Copeland 1936',NULL,0,0),(1307,1347,'description','Lager haut- bis lederartig, öfters sehr dick (4 bis 12 mm), dunkel stahlblau gefärbt, in grösseren Lappen sich ablösend. Fäden etwa 2.5 bis 3 um &nbsp;dick, gerade oder leicht gekrümmt, oft undeutlich gegliedert, in farblosen, 3 bis 4 um breiten Scheiden eingeschlossen. Veget. Zellen etwas kürzer oder ebenso lang als breit, mit blaugrünem Inhalte.','Rabenhorst ex Hansgirg 1892',NULL,0,0),(1308,1349,'diagnosis','Stratum tenue, valde expansum, pulchre aureo-fuscum. Fila flexuosa, intricata, aul subrecta, paralleliter disposita; vaginae arctae, papyraceae, demum in mucum diftluentes, chlorozincico iodurato baud caerulescentes. Trichomata dilute fusca, apice recta, haud attenuata, ad genicula non constricta, 2 [um crassa; articuli diametro breviores 1-1,5 um longi; dissepimenta non granulata; cellula apicalis rotundata, calyptra carens.','Gomont 1899',NULL,0,0),(1309,1354,'description','Lager lederartig oder fleischig, compact, schmutzig blau- oder dunkel-olivengrün. Fäden 1.5 bis 2.5 um dick, gekrümmt, dicht verflochten, undentlich gegliedert, mit eng anliegenden, dünnen, farblosen Scheiden und blass blaugrünem Inhalte','Hansgirg ex Hansgirg 1892',NULL,0,0),(1310,1356,'description','Stratum often poorly developed, up to 1.5 mm in thickness, epiphytic on other algae, soft, homogeneous, orange-brown. Trlchomes mostly closely packed, wavy to irregularly contorted, rarely parallel, 0.8-1.3 um in diameter wlth indistinct cross walls, not constricted at the cross walls, pale blue-green. Sheaths confluent into an amorphous sllmy matrix. Cells cyllndrical, 2 - 4 um in length, mostly with homogeneous contents, sometimes with 1-2 granules: cross malls not granulated. End-cells feebly broadened, truncate to subtruncate,<br>with slightly thlckened end membranes.','Copeland 1936',NULL,0,0),(1311,462,'description','Thallus ex filis dense intricatis constans substrato adhaerens in tegete tenui, aeruginosus in culturis juvenibus, tristiolivaceus in culturis vetustioribus. Fila in culturis juvenibus non ramosa vel raro pseudoramosa, plerumque isopolaria et non angustata, autem mimimum aloquot trichomatibus angustatis, 2.0–2.5 μm lata. Fila in cultura vestioribus non ramosa, saepe heteropolaria, apice basali uno tumido 4.0–4.8 μm lato, cito decrescentes ad 2.0–2.5 μm latos, subinde isopolare apicibus ambabus leviter tumidis. Vagina incolor, non lamellata, mollis et difluens ad basim, tenuis et vix evidens pro majore parte trichomae, post rumpens ultra apicem trichomae extensa. Trichomae indistincte vel leviter constrictae ad septa, isopolares ubi impigre crescentes, heteroplares in culturis vestioribus, 2.5–3.5 μm ad basim ubi constrictiones septi manifestissimae sunt, pro parte maxima 2.0–2.2 μm latae. Hormogonia dissolutione ad septum vel formatione necridiorum formantia, trichomae isopolares in dimidio rumpentes vel trichomae heteropolares ad apices frangentes, itaque hormogonis cellularum paucarum orientibus. Cellulae viridicaeruleae, typice granulo centrali uno ubi impigre crescentes, non granulares vel minute granulares in culturis vetustioribus, vacuolis formantibus in cellulis emorientibus, 1.3–3.0 μm longae<br>ubi impigre crescentes, saepe 4–7 μm longae in culturis vetustioribus. Cellulae apicales semper obtusirotundatae. Thylacoides in 3–6 strata, peripherales secus parietes externos et septa, typice non manifestae in trichomis vetustioribus per microscopium pallidum','Johansen et Kováčik in Johansen et al. 2011',NULL,0,0),(1312,1361,'description','Stratum sordide olivaceum. Fila primum sessilia caespitosa, deinde arete intricata, abundanter pseudo-ramosa, pseudo-ramis solitariis, curvatis. Vaginae distinctae hyalinae. Trichomata pallide aeruginosa paene hyalina, apicibus conicis, ad genicula haud constricta, protoplasmate homogeneo. Dissepimenta distincta haud granulata. Trich. diam. 2-3, cell. alt. 1-2 um','PLayfair 1915',NULL,0,0),(1313,1365,'diagnosis','Filis solitariis aut paucis aggregatis, gracilibus, elongatis, subrectis, 2.5 um crassis, repetite pseudoramosis, pseudoramis vulgo geminatis, rarius solitariis, erecto-patentibus; vaginis hyalinis, cylindricis, firmis, chlorozincico iodurato haud caerulescentibus; trichomatibus pallide aerugineis, ad genicula haud, constrictis, 1,5 um crassis; articulis diametro 2-6-plo longioribus, 3-9 um longis, protoplasmate granuloso farctis; dissepimentis pellucidis, passim inconspicuis, non granulatis; cellula apicali superne rotundata; calyptra nulla.','Frémy 1930',NULL,0,0),(1314,1370,'diagnosis','','Gomont 1899',NULL,0,1),(1315,1371,'diagnosis','','Gomont 1899',NULL,0,1),(1316,1371,'diagnosis','','Gomont 1899',NULL,0,1),(1317,1371,'diagnosis','Stratum tenue, roseum. Fila fragilia, recta, arcte intricala vel\' paralleliter disposita; vaginae saepius indistinctae, in mucum amorphum, chlorozincico iodurato caerulescentem diffluentes. Trichomata pallide roseola, moniliformia, apice raro et vix attenuata, 1,3-2 um crassa; articuli diametrum trichomatis fere aequantes aut vix superantes, 1,3-2,6 um longi. Protoplasma homogeneum. Cellula apicalis rotundata, rarius paulum elongata, attenuata, calyptra carens (v. s.).','Gomont 1899',NULL,0,0),(1318,1372,'diagnosis','Filamenta cylindrica, recta vel paucim irregulariter flexuosa, rare solitaria, praecipue in strata macroscopica intricata, saepe plus minusve paralleliter in coloniis ordinata, saepe cum vaginis tenuis, firmis, hyalinis. Trichomata cylindrica, pallide grise-aeruginosa, rare in protoplasmate cum granulis parvis, irreguaribus, ad dissepimenta non constricta, ad apices non attenuata (vel paucim attenuata in culturis), cum articulis paulo visibilis, plus minusve 2.4 µm lata, subinde repens. Cellulae longior quam latae, cylindricae, cellulae terminales cylindricae, apice complanate rotundatae et cum membrana exteriore paucim incrassata. Hormogonia curta, cylindrica.','Turicchia et al. 2009',NULL,0,0),(1319,1372,'description','Filaments straight or slightly irregularly flexuous forming macroscopic mats, often in more or less parallel oriented fascicles. Trichomes cylindrical, pale grey or greyish-green, not constricted at cross-walls, not attenuated towards ends (in cultures sometimes slightly attenuated), more or less 2.4 µm wide, with slightly visible cross-walls (staining!), slightly motile. Sheaths facultative, thin, smooth, firm, coloures. Cells longer than wide, sometimes with solitary, small irregular granules, end cells cylindrical, rounded, with thickened outer cell wall. Hormogonia cylindrical with indistinct cross walls, short.','Turicchia et al. 2009',NULL,0,0),(1320,1380,'description','L. strato valde expanso, cartilagineo, 3-5 mm crasso, obscure aerugineo vel vix colorato; filis flexuosis, densissime tortuoso-intricatis; vaginis tenuibus arctis, validis et achrois, crebro vacuis; trichomatibus angustissimis pallide aerugineis, inter cellulas non constrictis, apicibus rectis, obtusis et non attenuatis; cellulis diametro trichomatis paullo brevioribus, contentu homogeneo. Crass. fil. et trich 0.9 um; long. cell. 0.6-0.8 um.','West et West 1911',NULL,0,0),(1321,1384,'description','L. filis tenuissimis, in stratum luteo-ochraceum dense intricatis; vaginis initio tenuibus, hyalinis, demum crassioribus et ferrugineis; trichomatibus aerugineis, continuis, non torulosis, ad dissepimenta non constrictis, cellulis diametro trichomatis 5-6-plo longioribus; dissepimentis distinctis et non granulosis; cellula apicali cylindrica et obtusa, calyptra nula. Crass. fil 1.8-2.4 um; crass. trich. 0.8-0.9 um.','West 1904',NULL,0,0),(1322,1387,'description','Stratum atro-viride, tenuissimum, ·orbiculare , in foveolis rupium cretacearum nidulans. Vaginae in mucum gelatinosum amorphum, chlorozincico iodurato non crerulescentem omnino diffluentes. Trichomata pallide aeruginea, varie contorta, parallela, moniliformia, apice non attenuata, 1,5 um circiter crassa; articuli subquadrati vel diametro paulo breviores, 0,8 um ad 1,8 um longi; protoplasma haud granulosum; cellula apicalis rotundata; calyptra nulla.','Gomont 1892',NULL,0,0),(1323,1391,'description','Straturn mucosum, lamellosum, luteo- au fusco-aerugineum Vaginae i mucum gelalinosum fibrosum, chlorozincico iodurato non coerulescentem diffluentes. Trichomata plus minusve flexuosa, laete arugiea, varie inricata au subparallela, moniliformia, apie attenuata, 1.2 um ad 2,3 umcrassa; articuli subquadrati, 1.2 um ad 3 um longi; protoplasmahaud granulosum; cellula apicalis acute conica; calyptra nulla.','Gomont 1892',NULL,0,0),(1324,1394,'description','Strato, ut videtur, tenni, membranaceo, colore? (ut videtur aerugineo); filis plerumque plus minusve tortuosis et intricatis, interdum parallelis; vaginis mucosis, in muco hyalino difluentibus ; trichomatibus inter cellulas &nbsp;distincte coustrictis, saepe fere moniliformibus, apice non attenuato, cellula apicali rotundata; cellulis tarn longis quam latis vel ad duplo longioribus, cytoplasmate dilute aerugineo, homogeneo, rar egranulato; dissepimentis plerumque cum granulo magno distincto saepe deplanato in utraque parte, interdum modo in altera parte, vel sine granulis; calyptra nulla. Diam. trich. = \'0.8-1.2 um (interdum ad 1.5 um).','Fritsch 1912',NULL,0,0),(1325,109,'description','Plant mass grumose, gelatinous, olive-green, yellow to golden brown or light blue; cells spherical or oblong, 2-4-8-16 or more cells enclosed in the thick-sheathed envelope, lamellated or not, not confluent; colonial sheath very thick, stiff, with confluent lamellae at the margin of the envelope; sheath colorless, yellow or pink, becoming mostly yellowish brown with age; surface of sheath of both individual cells and the colonial envelope covered by short or long, minute or stout wart-like projections; cell contents homogeneous, or finely granulated (pseudovacuoles?), olive-green, bright blue-green or brownish green; cell division in two or three planes. Multiplication by vegetative division or fragmentation of the colony; aplanospores present.','Chu 1952',NULL,0,0),(1326,1400,'description','Plant mass grumose, crustaceous, gelatinous, olive-green; cells 2-4-8 in groups enclosed in a wide colorless or pinkish lamellated sheath; few to many small colonies in turn covered by a very wide, pale yellowish gelatinous envelope, spherical or oblong, or angled under mutual compression; wart-like projections on the surface of the sheath soft, short, with widened bases, numerous, and nearly covering the whole surface of the envelope; cells 7-9 x 12-16 um; colonies 70-250um in diameter; cell contents homogeneous or finely granulated (pseudovacuoles?), blue-green.','Chu 1952',NULL,0,0),(1327,492,'description','Solitary cyanoprocaryotic spherical cells, after division hemispherical, blue-green with homogeneous or slightly irregularly keritomic content, (3)3.5–4(4.5) um in diameter. Thylakoids in cells are arranged irregularly or ± parallely. Division by binary fission in two morphologically similar, hemispherical daughter cells.','Korelusová et al. 2009',NULL,0,0),(1328,1411,'description','Filaments prostrate or scattered among other filamentous algae, 1.4-1.6 um diam.; trichomes slightly constricted at the dissepiments, especially at the meristematic ends, not attenuated; cells aeruginous, quadrate, cross-walls plainly visible; apical cells rounded; sheath scarcely discernible, except in the very oldest parts, hyaline; branching very sparse.','Gardner 1927',NULL,0,0),(1329,1417,'description','Stratum tough, fibrous, not lamellate, usually with numerous included granules of silica, up to 3 cm in thickness, with corded streamer-like projections up to 10 cm in length and up to 1 cm in diameter, pale salmon to &nbsp;yellowish, whitish below. Filaments very long, straight, and mostly parallel, not crowded, trichomes not constricted at the cross walls, 0.4-0.6 um in diameter, pale blue-green, often yellowish and almost colorless; apices neither taperlng nor capitate. Sheaths hyaline, completely confluent Into a generally colorless matrix. Cells 1-2 diameters in length, 0.4-1.0 um Iong, and not granulated at the cross walls; cell contents homogeneous; cross walls inconspicuous and for the most part dificultly visible. Endc ells rounded, unmodlfled.','Copeland 1936',NULL,0,0),(1330,1422,'description','Ph. strato valde expanso, laete aeruginoso vel aeruginoso-caeruleo, usque ad 2 mm crasso; fills flexuosis densissime tortuoso-intricatis, vaginis in muco hyalino diffluentibus; trichomatibus angustissimis, laete aeruginosis, inter cellulas plus minusve constrictis, apicibus rectis non attenuatis nec capitatis; cellulis tam longis quam latis vel paullo longioribus, contentu homogeneo. Crass, trich. 0.8-0.9 um, &nbsp;long. cell. 0.8-1.1 um','West &amp; West 1911',NULL,0,0),(1331,1424,'description','Genus showing typical Nostoc-like morphology with rounded terminal cells and presence of both terminal and intercalary heterocytes. Coiling is easily visible though may vary to different degrees. As of now, one of the characteristic features is the presence of well-defined constrictions between the cells, thus giving the barrel-shaped vegetative cells an enhanced look. The genus may occur in soil, freshwater and seepages. The filaments can be very long in some cases, while others may have a moderate number of cells. The most important criterion for the establishment as a new genus is the distinct phylogenetic clustering based on the 16S rRNA gene.','Saraf et al. 2019',NULL,0,0),(1332,1425,'description','Macroscopic greenish mat dwelling in the natural habitat; grows more or &nbsp;less in seepages where the confluence of little amount of water and soil &nbsp;is seen. Appears with a small amount of mucilage with a soft texture. &nbsp;Collection from nature is easy as the mucilage is not very dense. The &nbsp;laboratory-grown culture also has a mat-like appearance, although &nbsp;colonies at the ends may appear more discrete. Under themicroscope, &nbsp;usually appears light green in colour. Extremely long filaments have a &nbsp;large amout of visible cells. Vegetative cells are usually barrel &nbsp;shaped, though sometimes may also appear a bit longer than the width. &nbsp;Constrictions are very prominent in between the cells. Cellular contents &nbsp;seem to appear slightly granular giving the entire filament a slightly &nbsp;textured appearance. The terminal vegetative cells range in size &nbsp;from3.44 to 5.33 μmlong to 3.95–4.04μm wide. The intercalary vegetative &nbsp;cells range in size from 3.83 to 5.09 μm long to 3.44–5.33 μm wide. &nbsp;Sheaths are distinct, appearing throughout the trichome, with a &nbsp;slightly mucilaginous appearance. In most of the cases observed, the &nbsp;heterocytes appear at both the ends of the filament. Heterocytes are &nbsp;yellowish in colour and usually appear almost spherical. The terminal &nbsp;heterocytes range in size from 4.11 to 5.46μm long to 4.41–5.21 μm wide. &nbsp;The intercalary heterocytes range in size from 4.72 to 6.32μm long to &nbsp;4.98–6.03μm wide. Akinetes were not observed in any stage of the life &nbsp;cycle.','Saraf et al. 2019',NULL,0,0),(1333,1426,'description','Macroscopic mat with a dark greenish colour in the natural habitat. Appears very clearly in almost dry soil as mats having feathery exterior appearance. The mats have little mucilage around them and picking the mat from nature is easy. Laboratory-grown cultures appear slightly leathery in appearance and grow as discrete colonies on the plates. Appears dark greenish blue in the microscope with cellular contents being densely granular. Extremely long filaments with a large number of cells are visible and even the comparatively shorter filaments also have more than 15 cells and terminal heterocytes. The vegetative cells appear barrel shaped with some cells being larger than the routine vegetative cells. The presence of a small amount of mucilaginous sheath is evident all around the trichome. Constrictions are prominent between the adjacent cells. The heterocytes appear yellowish in colour. Heterocytes are present both at the intercalary and terminal positions. The shape of the heterocyte varies, with the intercalary heterocytes being spherical while the terminal heterocytes appear slightly oblong in shape. Terminal heterocytes appear at both the ends of the trichome in many cases. The terminal vegetative cells range in size from 3.24 to 4.22 μm long to 3.57–3.74μm wide. The intercalary vegetative cells range from 3.58-4.93 μm long to 3.79–4.48μm wide. Terminal heterocytes range in size from 5.26 to 6.51 μm long to 4.21–5.21 μm wide. Intercalary heterocytes range in size from 4.91 to 6.89 μm long to 4.17–5.70 μm wide. Neither the natural occurring sample nor the laboratory-grown culture showed any evidence of akinete formation.','Saraf et al. 2019',NULL,0,0),(1334,1427,'description','Macroscopic light blue-green mats in natural habitat; appear as soft textured entities as wild specimens, slightly mucilaginous, moist and slightly leathery in nature. Mats can be picked up and separated easily from each other. In culture, colonies start growing as light blue-green filaments with an irregular pattern of growth which is multidirectional and has a mat-like appearance. Colonies appear leathery and moist on plates. Filaments appear loosely packed and irregular, with occasional slight coiling. Sheaths are distinct, appearing throughout the trichome, with a slightly hyaline appearance, and are prominent at the ends of the trichome especially around the heterocytes. Older cultures grown in nitrogen-deficient medium (around 5 months) turn yellowish in liquid medium, but again turn green after inoculation into fresh nitrogen-deficient medium. Trichomes are usually long, consist of 31–152 cells and are highly constricted at the cross-walls, which are evident in all stages of growth. Cellular contents are typically granular. Vegetative cells are 3.63–4.92 μm in length and 3.46–3.81μm in width, usually barrel-shaped. Terminal vegetative cells are 3.64–4.29μm in length and 3.30–3.49μm in width, with perfectly curved ends. Vegetative cells near to intercalary heterocytes are 3.43–4.46 μm in length and 3.51–3.53 μm in width. Vegetative cells near to terminal heterocytes are 3.93–4.79 μm in length and 3.37–3.77 μm in width. Heterocytes are both intercalary and terminal; terminal heterocytes are 4.74–5.78 μm in length and 3.39–4.49 μm in width, spherical with slightly elongated ends; intercalary heterocytes are 4.74–6.00 μm in length and 4.45–5.27 μm in width and spherical in shape. Akinetes were not observed.','Sudarkar et al. 2017',NULL,0,0),(1335,422,'description','Colonies microscopic, more or less spherical or oval, sometimes composed of subcolonies, rarely irregular when old, free-living, usually floating in plankton, enveloped by fine, colourless, usually not sharply defined, sometimes indistinct mucilage; mucilage limited to just around the peripheral layer of cells or forming a gelatinous layer (margin) around cells. Cells more or less in one layer on the colonial periphery, spherical or hemispherical after division, usually slightly or distinctly distant from one another, with or without aerotopes. Mucilage homogeneous, fine, never structured, without any stalks in the colonial center.&nbsp;','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1336,1441,'description','Filis late expansis, tortuoso-intricatis, hyalinis aut pallidissime coerulescentibus; vaginis arctis, achrois; articulis diametro brevioribus aut subaequalibus, ad 2-2,5 latis; pseudoramulis solitariis, patentibus, raro geminis.&nbsp;','Borzí 1892',NULL,0,0),(1337,1443,'description','Fäden 1.5 bis 2 um dick, einzeln oder büschelig gehäuft, meist leicht gekrümmt und verworren, undeutlich gegliedert, mit dünnen, eng anliegenden, leicht zerfliessenden Gallertscheiden und blass blaugrünem, bis fast farblosem Inhalte. Veget. Zellen 1 bis1.5 mal so lang als breit.','Hansgirg 1892',NULL,0,0),(1338,867,'description','Roseum vel rubro-fuscum, stratum expansum in rupibus marinis formans, aut in Algis majoribus insidens. Fila intricata, elongata, flexuosa, abundanter, etiam repetite pseudo-ramosa; pseudo-rami geminati, patentes, elongati, lilo primario tenuiores, subflagelliformes. Vaginae hyalinae, crassiusculae, chlorozincico iodurato vis coerulescentes. Trichomata roseola, brevi-articulata, torulosa, 1,2-2 um crassa; articuli diametro usque ad triplo breviores. Protoplasma homogeneum; cellula apicalis rotundata','Gomont 1899',NULL,0,0),(1339,1449,'description','Lager dünnbäutig, nicht selten weit ausgebreitet, von blass bläulicher, gelblich- bis graugrünlicher Farbe oder schmutzig gelblichgrau, in feuchtem Zustande meist schleimig. Fäden mit der Scheide 2 bis 4 um dick, mit einfachen oder doppelten Seitenästchen, mehr oder minder deutlich gegliedert. Veget. Zellen 1 bis 3mal so lang als breit, mit hell bläulichgrünem, bis fast farblosem Inhalte. Scheiden dünn, eng anliegend, meist farblos.','Hansgirg 1892',NULL,0,0),(1340,1470,'description','Cells hemispherical to rounded, solitary or rarely grouped in few-celled colonies. Cell content green, blue green to olive green, homogeneous to granulate, fasciculate thylakoids. Sheaths hyaline surrounding the cells, simple to lamellate. Reproduction only by binary fission in three irregular planes.&nbsp;','Gama et al. 2019',NULL,0,0),(1341,1471,'description','Cells hemispherical to rounded, 8.3–(11.6)–15.5 μm diam., solitary or rarely grouped in few-celled colonies. Sheaths hyaline surrounding cells and colonies, smooth or rarely lamellate. Cell content granulate, green to blue-green. Nanocytes never observed.','Gama et al. 2019',NULL,0,0),(1342,1472,'description','Cells hemispherical to rounded, 8.7–(10.8)–13.9 μm diam., solitary or rarely grouped in few-celled colonies. Sheaths hyaline surrounding cells and colonies, smooth or rarely lamellate. Cell content intensely granulated, blue-green to yellowish-green. Nanocytes never observed.','Gama et al. 2019',NULL,0,0),(1343,1473,'description','Cells hemispherical to rounded, solitary or rarely grouped in few-celled colonies. Cell content green olive to purple brownish, homogeneous to granulate, fasciculate thylakoids. Hyaline to generally intense red sheaths surrounding cells, simple to lamellate. Reproduction by binary fission in three irregular planes and nanocytes present.','Gama et al. 2019',NULL,0,0),(1344,1474,'description','Cells hemispherical to rounded, 4.7–(6.7)–11.9 μm diam., solitary or rarely grouped in few-celled colonies. Hyaline to intense red-coloured sheaths surrounding cells and colonies, smooth or rarely lamellate. Cell content finely granulated, purplebrownish to green-brownish. Nanocytes present, formed by polygonal cells surrounded by redcoloured sheaths.','Gama et al. 2019',NULL,0,0),(1345,1501,'description','Colonies are free-living, spherical or irregularly oval, and sometimes composed of subcolonies. They have a central system of thick mucilaginous stalks that are nearly pseudodichotomously divided and may be diffuse within the colony. Stalks widen at the ends and envelope individual cells with a thin mucilage layer. Cells are slightly elongate, obovate, or club-shaped, and radially oriented more or less at the colony periphery, which is sometimes enveloped by a fine, colorless, and diffuse mucilage. Cells have a homogeneous pale or bright blue-green, olive-green, or red content and are (4.2)6-12(15) X 2-8(13.2) μm. After division, the cells may remain joined together and form a characteristic cordiform shape. Cells in colonies are slightly distant and sometimes slightly radially displaced from one another. Cell division occurs in two planes in successive generations, perpendicular to one another and to the colony surface. Reproduction is by colony disintegration.','Komárek 2003',NULL,0,0),(1346,1520,'description','Forming firm, cartilaginous, suborbicular or depressed-hemi-spheric, lubricous, bluish olivaceous or light green, often decolorate discs or cushions 2-7.5 cm broad and 1-2.5 cm thick, becoming corneous or corneous-coriaceous and only 1-3 mm thick on drying, rather conspicuously lamellate, the lamellae (when fresh) mostly 300-600 um thick, all except the youngest consisting chiefly of empty hyaline more or less confluent, though usually easily perceptible, sheaths with occasional flexuous or contorted living filaments and inclusions of foreign algae and varied detritus; filaments of the superficial lamella crowded, usually flexuous or contorted, occasionally rather strict and suberect; vaginae close, mostly inconspicuous, not affected by chlor-zinc-iodine ; trichomata pale olivaceous, 1. 5-1.8 um thick, not constricted at the septa, the apex straight, not attenuate; cells 2-6 times as long as broad, 3-9 um long, the apical rounded, calyptra none.','Howe 1918',NULL,0,0),(1347,671,'description','Filamentous; filaments solitary, rarely (in old stages) tangled together, isopolar, waved or irregularly spirally coiled (particularly in the middle parts), sometimes with more or less erected and free ends, creeping on the substrate (usually coiling about other filamentous cyanophytes or algae) and attached to it by the central part, with simple, firm but thin, colourless sheath enveloping the trichome and opened at the apex, unbranched or very rarely falsely branched (usually with one lateral branch), 1.5-12 (?) μm wide. Trichomes cylindrical, with cylindrical cells, sometimes with a little modified morphology of cells in apical parts (trichome ends more constricted at cross walls or slightly widened), unconstricted or constricted at the cross walls in the middle part, not attenuated, immotile. Cells +/- isodiametric, slightly shorter or up to distinctly longer than wide, cylindrical or sometimes barrel-shaped at the ends, without aerotopes, pale greyish, blue-green or yellowish; end cells rounded, without thickened cell wall or calyptra. Heterocytes and akinetes lacking.','Komárek 1992',NULL,0,0),(1348,671,'reproduction','Cells divide by symmetrical, crosswise binary fission, cells grow into the original size before next division. Reproduction by immotile hormocytes which adhere lengthwise by their sides to the substrate and grow up at both poles. Hormocytes liberate from trichomes in their apical parts without help of necridic cells.&nbsp;','Komárek 1992',NULL,0,0),(1349,402,'description','Colonies endolithic, irregularly reticulate, composed of randomly divaricate and anastomozing, more or less limited and firm mucilaginous, filamentous strands, colourless, homogeneous, inside with uniseriate, irregular rows of cells, oriented parallel to the strands; in places with widened mucilage, the cells are irregularly distributed; without special envelopes around them. Cells spherical, ellipsoidal or oval, near to one another after division.','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1350,402,'reproduction','Cell division by binary fission, probably only in one plane in successive generations, perpendicular to the length of the strands. Reproduction possibly by liberation of solitary cells.','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1351,1532,'description','Colonies microscopic, in form of mucilaginous spheres, simple or compound, with several spherical subcolonies, sometimes slightly irregular oval, free floating in plankton or metaphyton, consisting of fine, homogeneous, colourless mucilage; beneath the surface is a layer of irregularly, more or less tangentially arranged cells, sometimes overlapped by a thin, but distinctly delimited layer of colonial slime. Cells oval or rod-shaped, up to several times longer than wide, usually slightly distant one from another or in small clusters, pale blue-green, without aerotopes. Without stalks in the colonial center. Cell division by transverse binary fission into two equal parts, perpendicular to the longer cell-axis, in one plane in successive generations. Cells become more or less the original size before the next division. They soon separate from one another after division and usually shift to the parallel position; rarely remaining in short rows. Reproduction by «budding» of daughter spherical colonies from the surface of the old mother colony, or by disintegration of colonies into small clusters of cells or even solitary cells.&nbsp;','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1352,1569,'description','The thallus was composed of solitary cells or, more commonly, microscopic colonies, forming extended and compact multicolonial groups (Fig. 1 A–B). Colonies were mostly irregular, sometimes rounded, with several cells (up to 32–64 cells or more) (Fig. 1 C–D). Cells were cylindrical with rounded ends when isolate (Fig. 1 F–G), sometimes irregular by mutual extrusion when in dense colonies (Fig. 1 C–D). Cells were 2.8–3.7 μm long (mean = 3.3 ± 0.3 μm, n = 40), 2.0–2.7 μm in diameter (mean = 2.2 ± 0.2 μm, n = 40), 1.3 to 1.7 × longer than wide (mean, 1.5 ×) (Fig. 1 F–G). With pressure cells were easily removed from colonies while the mucilaginous envelope remained (Fig. 1 E). The chromatoplasm and centroplasm were usually recognizable under light microscopy (Fig. 1 E–G).<br>TEM showed that the cells were enveloped by firm and compacted mucilaginous sheath (Fig. 2 A–B). The cell wall consisted of three layers measured about 40 nm width, in which the electron-dense peptidoglycan layer (Fig. 2 C, E). The centroplasm and chromatoplasm were usually recognizable. DNA fibrils and spherical polyphosphate bodies were seen in centroplasm via TEM (Fig. 2 C, F). The chromatoplasm was composed of phycobilisomes, glycogen granules, thylakoids and their associated structures (Fig. 2 E–F). The ultrastructure showed that three to five parietal thylakoids could be parallel to the cell wall (Fig. 2 C, E–F). Binary fission occurred via a constrictive pinching mechanism in which all cell wall layers were involved (Fig. 2 D).','Zhang et al. 2019',NULL,0,0),(1353,764,'description','Photobiont of Dictyonema coppinsii; filamentous. Trichomes isopolar, uniseriate, cylindrical, formed by low rectangular cells 15–20 mm wide and 5–10 mm high, with blue-green 2014 Dictyonema coppinsii—Lu¨cking et al. 265 pigmentation embedded in a thin, dense, gelatinous, hyaline sheath; terminal cells smaller, 7–13 mm wide and 3–7 mm high. Branching rare, representing true branching of T type. Heterocytes sparse to frequent, intercalar, yellowish, 12–18 mm wide and 4–8 mm high. Asexual reproduction not observed.','Lücking et al. 2014',NULL,0,0),(1354,705,'description','Filamentous or broken into irregular clusters of rounded cells. Trichomes isopolar, uniseriate, cylindrical, formed by rectangular cells with blue-green to olive-green pigmentation embedded in a thin, dense, gelatinous, hyaline or brownish sheath (Fig. 1C); terminal cells smaller and often yellow rather than blue-green but not rounded or hair-like (Fig. 1E). Branching rare, representing true branching of T or akin towards V type, with the division plane periclinal or slightly oblique (Fig. 1D). Heterocytes frequent, intercalar (Fig. 1C). Asexual reproduction rare, by hormogonia (Fig. 1F) and akinetes.','Lücking et al. 2014',NULL,0,0),(1355,423,'description','&nbsp;Colonies microscopic, free floating, more or less spherical, composed of radially and slightly irregularly divaricate thick, tube-like, colourless stalks, originating from the colonial center. Cells narrower than stalks, situated within the end of stalks; the whole stalk system with cells is enveloped by the common, fine, diffluent, colourless mucilage; stalks slightly distant from one another. Cells in strings solitary or grouped in twos after division, geminate.&nbsp;','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1356,424,'description','Snowella comprises free-living, spherical or oval microscopic colonies, sometimes composed of subcolonies, that have a central system of thin, nearly pseudodichotomously divided gelatinous stalks (may be confluent) that bear cells at their ends (periphery of colony). Colonies are enveloped by very fine, unstructured, and diffuse mucilage. Cells are spherical or slightly radially elongated, and pale blue-green, olive green, or yellowish in color; one species may be pinkish. Two species have one or a few central aero-topes. The cells are 0.6-4.2 μm in diameter (or long). Cell division is by binary fission in two planes, perpendicular to one another and to the colonial surface. Reproduction is by disintegration of colonies.','Komárek 2003',NULL,0,0),(1357,1118,'description','Filaments composed of a uniseriate trichome. Sheath usually present, thin, colorless. Filaments gliding and attenuated at the end. Cells longer than wide, with peripheral thylakoids. Filaments and single cells within are bright green. Both external and cross cell walls undulated.','Zimba et al. 2017',NULL,0,0),(1358,1119,'description','Filaments are rarely solitary, usually forming clusters or mats on substrate, rarely freely floating; filaments are undulated, narrowing at the ends, with thin sheaths, and are unbranched. Filaments are 1.3-3.3 um and the width is 0.5-2.5 um wide and exhibit gliding motility. Cells are cylindrical, up to 3.1 um long, with peripherally arranged thylakoids. Polyphosphate bodies and cyanophycin granules occur in cell corners with micro plasmodesmata present between cross cell walls. The molecular sequence closest affiliations are to Prochlorothrix and Limnothrix. Carotenoids include aphanizanthin, zeaxanthin, and b-carotene. Chlorophyll a and phycobilins (including PC, allophycocyanin, and PE) are present. Cellular fatty acids include palmitic acid (C16:0), palmitoleic acid (C16:1), pentadecylic acid (C15:0), and oleic acid (C18:1x9).','Zimba et al. 2017',NULL,0,0),(1359,425,'description','Colonies more or less spherical or irregular oval, commonly composed of subcolonies, free-living, usually with a narrow, colourless enveloping mucilaginous layer. &nbsp;In the center of colonies is a system of radially and more or less parallely oriented, simple, unbranched stalks, which split along their whole length after cell division; stalks thick, usually as wide as the width of cells, commonly densely packed together and so causing the radial lamellation of the central colonial mucilage (staining !); the stalk system sometimes diffluent within old colonies. Cells rarely almost spherical, usually slightly elongate, widely oval, oval or obovoid, separating from one another immediately after division, but in old colonies very densely, radially aggregated in the peripheral layer.&nbsp;<br>Cell division in two planes perpendicular to one another in successive generations, and perpendicular to the colony surface; reproduction by disintegration of colonies and especially by liberation of solitary cells (sometimes spontaneously) from the colony (expulsingcells).','Komárek &amp; Anagnostidis 1998',NULL,0,0),(1360,1628,'diagnosis','Morphologically identical to Crocosphaera, but differing phylogenetically and having shorter BoxB helix in the 16S-23S ITS (26 nt vs. 32–33 nt). Differs from other morphologically similar coccoid genera through the absence of mucilage surrounding cells as well as by the ability to fix atmospheric N2. Note: observations are based exclusively on culture material.','Mareš et al. 2019',NULL,0,0),(1361,1628,'description','Cells solitary or briefly in pairs following binary fission, without mucilage, short bacilloid to spherical, 1.0–2.0 times as long as wide. Diazotrophic.','Mareš et al. 2019',NULL,0,0),(1362,1629,'diagnosis','Morphologically identical to Crocosphaera, but differing phylogenetically. Differs from other morphologically similar coccoid genera through the absence of mucilage surrounding cells as well as by the ability to fix atmospheric N2. Differs from the Zehria strains from Singapore in its smaller cell size. Note: observations are based exclusively on culture material.','Mareš et al. 2019',NULL,0,0),(1363,1629,'description','Cells solitary or briefly in pairs following binary fission, without mucilage, short bacilloid to spherical, 1.0–1.7 times as long as wide, 4–5.2 um wide, 4–8 um long, dividing cells showing constriction of the wall, 7–11 um long.','Mareš et al. 2019',NULL,0,0),(1364,1630,'description','Thin trichomes (less than 3 lm width) composed by cylindrical, isodiametric or elongated cells and more or less conical terminal cells (Fig. 7A1, 7B1 and 7C1). Large amount of slime can be observed surrounding the filaments (Fig. 7A2, 7B2 and 7C2). Parietal arrangement of the thylakoids (Fig. 7A3, 7B3 and 7C3). Terminal cells are more or less conical (Fig. 7B3 and 7C3), sometimes rounded with calyptra (Fig. 7A4, 7B4, 7C4). Reproduction by hormogonia, necridic cells not observed. Motile.','Brito et al. 2017',NULL,0,0),(1365,1631,'description','Trichomes straight or curved, irregularly clustered or in bundles, forming ‘‘leathery” mats, motile. Cylindrical cells 1.5–2.8 um wide, 2–6 um long, isodiametric or elongated (Fig. 7A1 and 7A3). The terminal cells are more or less conical, sometimes rounded with calyptra (Fig. 7A4). Slime surrounding the filaments can be observed (Fig. 7A2), structured sheaths not visible. Contains PE and PC (Fig. 2C). 16S-23S rRNA ITS region 444 nucleotides long: D1-D10 helix with 90 nucleotides; Box-B 35 nucleotides long with 4 nucleotides in the terminal loop; tRNAIle with 74 nucleotides (Fig. 8 and Table S3).','Brito et al. 2017',NULL,0,0),(1366,494,'description','Spherical cells with 2.0–3.0 lm in diameter. Blue- or olivegreen cells solitary or more often forming aggregates (Fig. 1B and E) surrounded by slime (Fig. 1C and E). Irregular arrangement of the thylakoids (Fig. 1D), and presence of long and abundant pilus-like structures extending to adjacent cells (Fig. 1F). Contains phycocyanin (PC) but not phycoerythrin (PE) (Fig. 2A). 16S-23S rRNA ITS region 367 nucleotides long: D1-D10 helix with<br>18 nucleotides; Box-B 29 nucleotides long with 10 nucleotides in the terminal loop; tRNAIle and tRNAAla with 74 and 73 nucleotides, respectively (Fig. 3 and Table S3).','Ramos et al. 2017',NULL,0,0),(1367,495,'description','Thallus brown, rarely red- or violet brown. Proximal part of pseudofilament uni-, bi- or multiseriate, with more or less spherical, polygonal rounded or oval cells 2.5–5.5 um in diameter. Distal part of thallus usually uniseriate, cells club-shaped or cylindrical, 3–5 um wide and up to 10 um length (terminal cells rarely up to 20) (Fig. 5A). Colourless multi-layered sheath, easily observed by TEM (Fig. 5C and D). Colonies held together by extracellular polymeric substances (EPS) (Fig. 5B and E) from which the pseudofilaments emerge (Fig. 5D–F). Cells divide by binary fission, reproduction by baeocytes. The thylakoids arrangement is parietal (Fig. 5C and D). Contains PE and PC but high PE:PC ratio (Fig. 2B). 16S-23S rRNA ITS region 657 nucleotides long: D1-D10helix with 61 nucleotides; Box-B helix 22 nucleotides long with 6 nucleotides in the terminal loop; tRNAIle and tRNAAla with 74 and 73 nucleotides, respectively (Fig. 6 and Table S3).','Ramos et al. 2017',NULL,0,0),(1368,1632,'description','Thallus filamentous, blue-green (Fig. 9A and B), without sheath or with very fine mucilaginous layer around the trichome, immotile, forming a firm biofilm. Trichomes slightly constricted at the cross walls. Cylindrical cells 1.2–2.1 um wide and 2–4 um long (Fig 9C), apical cells shortly narrowed or rounded, without calyptra. Parietal arrangement of the thylakoids (Fig. 9C). Contains PC but not PE (Fig. 2F). 16S-23S rRNA ITS region 447 nucleotides long: D1-D10 helix with 60 nucleotides; Box-B 30 nucleotides long with 5 nucleotides in the terminal loop; tRNAIle with 74 nucleotides (Fig. 10 and Table S3).','Brito et al. 2017',NULL,0,0),(1369,1633,'description','Trichomes with parietal arrangement of thylakoids (distinguishable centro- and chromatoplasm), constricted at the cross walls, cells shorter than wide or almost isodiametric. End of filament is distinctly wider and cells are more constricted than the normal vegetative cells. Colourless fine sheath, sometimes wider and layered. Reproduction by hormogonia, necridic cells present.','Brito et al. 2017',NULL,0,0),(1370,1634,'description','Filaments forming tuft-like aggregates, trichome olive green to dark brown (Fig. 11A and B), (1.5) 1.9–4 (5.5) lm wide, cells length irregular (0.5–5 lm), mostly shorter than wide or isodiametric (Fig 11D and E). Cells barrel shaped with sharp constrictions at the cells junctions (Fig. 11C–F), and at the end of filaments are deeply constricted, more spherical and slightly wider that normal cells, later separated by necridic cells as hormogonia (Fig. 11F). Colourless sheath, well defined sometimes wider and layered (more visible with TEM, Fig. 11C). Contains the phycobilin pigments phycoerythrin (PE) and phycocyanin (PC) (Fig. 2G). 16S-23S rRNA ITS region 553 nucleotides long: D1-D10 helix with 58 nucleotides; Box-B 56 nucleotides long with 4 nucleotides in<br>the terminal loop; tRNAIle and tRNAAla with 74 and 73 nucleotides, respectively (Fig. 12 and Table S3).','Brito et al. 2017',NULL,0,0),(1371,1635,'diagnosis','Akin to Pleurocapsa in morphology, differing by random baeocyte formation throughout younger pseudodofilaments, and phylogenetically (16S, rbcX phylogenies; ITS structures; 16S, rbcX p-distance), more closely related to a clade containing an undescribed baeocyte producer Pleurocapsalean cyanobacterium (strain ATA3-5Q-K04-AU5, GenBank MG869762), than to Pleurocapsa sensu stricto.','Shalygin et al. 2019',NULL,0,0),(1372,1635,'description','Thallus attached to the substrate in both natural populations (?) and culture, forming blackish spherical aggregates, later having almost uniform substrate coverage. Frequent three-dimensional macrocolonies epilithic (not endolithic). Pseudofilaments moderately long, uni- or multi-seriate, forming irregular groups of cells with pseudodichotomous branches located peripherally. Stages with only sarcinoid cells rare. Sheaths thin, colorless, tightly attached to the cell walls. Common and individual F layers present. Cells of various shapes and sizes, with enlarged mother cells common in culture. Cytoplasm usually homogeneous, sometimes granular, heterogeneous before baeocyte formation. Recently released baeocytes dividing in 2 planes, typically crosswise, with older cells dividing in various planes. Reproduction by motile (?) baeocytes without individual F layer; mother cells containing 2–24 baeocytes. Baeocytes develop throughout pseudofilaments randomly in any actively growing cells (i.e., sarcinoid, coccoid, elongated, pseudodichotomously divaricated). Formation of baeocytes within small, young coccoid cells observed.','Shalygin et al. 2019',NULL,0,0),(1373,1636,'diagnosis','Morphologically similar to Pleurocapsa sp. (strain HA4230, GenBank KC525081), differing by phylogenetic position, 16S p-distance value (&gt;4% dissimilarity) as well as sequential and minor structural dissimilarities of ITS region. Baeocyte formation throughout the pseudofilaments and thallus.','Shalygin et al. 2019',NULL,0,0),(1374,1636,'description','Macroscopic colonies in the form of dark pigmented clumps arising from the substrate. In culture, growing attached to the sides of the culture vessel, surface of bricks, carbonate rocks, and seashells. Young stages composed of radial to irregular oriented pseudofilaments with pseudodichotomous branches pointed outward from the colony center, later growing in irregular multiseriate sarcinoid colonies, usually pseudodichotomously divaricate at the margins. Sheaths firm, thin, colorless, both common and individual. Pseudofilaments uni- or multiseriate, frequently pseudodichotomously branched, pale blue-green, olive to olive-red in color, up to 35 lm long. Cells spherical, elongated, occasionally with “Chroococcus-like” appearance, sometimes with granular cytoplasm, 5–7 lm in diameter.','Shalygin et al. 2019',NULL,0,0),(1375,1637,'description','Thallus microscopic, fasciculate, 70-96 μm wide, 820–868.5 μm long, formed by several (6-10) trichomes densely aggregated. Trichomes straight, not attenuated, strongly constricted, without mucilage. Cells elongated or more rarely barrel shaped, with gas vesicles, 4.6–7.1 μm wide, 4.9–7.4 μm long; apical cell hemispheric or elongated.','Sant Anna et al. 2018',NULL,0,0),(1376,1638,'diagnosis','Thallus dark green or blackish green, forming mats. Filaments solitary or entangled, more or less straight or wavy. Trichomes cylindrical, pale blue–green, not or slightly constricted at cross-wall, with a thin sheath colorless, motility present. Cells mainly longer than wide (rarely isodiametric), 2.4–3.4 μm wide. Cell content homogeneous, plenty of small granules. Apical cell conical-rounded, slightly hooked or bent, sometimes with extrusions. Aerotopes absent.','Cellamare et al. 2018',NULL,0,0),(1377,1640,'diagnosis','Thallus emerald green, diffluent, forming thin mats. Filaments solitary, nearly straight, flexuous, blue-green or yellow-green. Trichome cylindrical, slightly constricted at the crosswalls, very slightly attenuated at the ends, sometimes with a very fine, attached and diffluent sheath. Cells longer than wide, 2.4–3 μmwide. Cell content with a large refractive granule on either or both sides of the cross-walls. Apical cell rounded, hemispherical, often with a large granule (aerotope?). Motility present.','Cellamare et al. 2018',NULL,0,0),(1378,1642,'description','Thallus bright-green, forming thin, flattened and expanded mats. Filaments solitary or entangled, nearly straight or slightly flexuous. Trichomes thin, cylindrical, pale blue-green, not attenuated at the ends, slightly constricted at cross-walls, sheaths thin, attached, diffluent, colorless. Cells longer than wide, 1.5–2 μmwide. Apical cell rounded, with a refractive granule (numerous aerotopes with TEM). Motility present.','Cellamare et al. 2018',NULL,0,0),(1379,1643,'diagnosis','Thallus bright-green, forming mats. Filaments solitary or entangled, straight or slightly arcuated, flexuous, sometimes undulated. Trichomes pale blue-green, thin, very constricted at cross-walls, not attenuated towards the ends, with a firm sheath with a thin transparent zone. Cells cylindrical, always longer than wide (up to 3 times), 0.9–1.5 μm wide. Apical cell conical-rounded. Motility was not observed.','Cellamare et al, 2018',NULL,0,0),(1380,1644,'description','Colonies macroscopic, irregularly clustering, gelatinous, free–living on wet rocky wall, blue–green. Filaments flexuous, freely entangled, sheath usually present, colourless. Vegetative cells barrel–shaped, and more or less longer than wide. Heterocytes and akinetes not known.','Cai et al. 2019',NULL,0,0),(1381,1645,'description','Colonies are macroscopic, gelatinous, irregularly clustered, free–living on wet rocky wall in the form of irregular, amorphous, blue–green gelatinous clusters. Filaments flexuous, freely entangled. Sheath usually present, colourless. Vegetative cells barrel–shaped, 3.1– (4.3)–5.4 μm long, 2.5– (3.2)–3.8 μm wide, length: width ratio 1.3. Heterocytes and akinetes were not observed during 3 years of observation. In the BG11 and BG110 medium, the novel strains were never shown to form heterocysts. The strains did not grow in the BG110 medium, since the cultures started to bleach after 4 days of incubation in this medium.','Cai et al. 2019',NULL,0,0),(1382,1646,'description','In nature, macroscopic colonies free-living on wet rocky walls; in culture, forming macroscopic masses on test tube bottom. Colonies not forming spherical colonies, but several small young microscopic colonies clustered to create macroscopic colonies with densely entangled filaments. Colonies amorphous, fine, thin, mucilaginous, yellow-brownish or olive green. Sheath colourless, usually distinct at colony margins. Trichomes uniseriate or biseriate only in short segments. Filaments densely entangled, forming compact young microcolonies and enclosed by firm mucilage layer. Cells barrel shaped or almost spherical; heterocytes uncommon, cap shaped, slightly smaller than vegetative cells, terminal in young colonies, intercalary in old colonies. Akinetes not found.','Cai et al. 2019',NULL,0,0),(1383,1647,'description','Macroscopic thallus fine, thin and mucilaginous and growing on wet rocky walls. Thalli usually composed of a few colonies, up to 2 mm in diameter, yellow-brownish or olive green. Sheath colourless, usually visible in marginal parts of colonies. Trichomes uniseriate or only in short segments biseriate. Filaments usually densely entangled, forming compact young microcolonies, with several young microscopic colonies eventually aggregating into larger compact macroscopic masses. Cells barrel-shaped or almost spherical, 2.6–5.3 μm long, 2.7–5.7 μm wide, length:width ratio 0.96. Heterocytes uncommon, cap-shaped, slightly smaller than vegetative cells, 1.7–(2.3)–3.3 μm long, 2.2–(2.9)–3.7 μm wide, terminal in young colonies, intercalary in old colonies. Akinetes were not observed during 2 years of observation.','Cai et al. 2019',NULL,0,0),(1384,1648,'description','Filaments solitary, lacking sheath material. Trichomes motile, without branching, straight to curved, flexuous, thin, less than 3 μm in diameter. Hormogonia formed by simple fragmentation without necridia. Cells nongranular or with colored elongated granules, with polar bodies resembling aerotopes typically at crosswalls, with parietal thylakoids.','Akagha et al. 2019',NULL,0,0),(1385,1649,'description','Thallus in young cultures a thin mat coating the walls and bottom of culture vessel, later forming a floating mat, consistently pale blue–green. Sheaths always absent. Trichomes motile, straight to sinuous, flexuous, not coiled, without false branching, not constricted to slightly constricted at the crosswalls, 2–2.5 μm wide. Hormogonia form by simple fragmentation, without necridia, as short as a single cell in length. Cells nongranular or possessing elongate bluish and brownish granules, often with polar bodies resembling aerotopes at the crosswalls, with parietal thylakoids which are detectable in some cells as the presence of peripheral chromatoplasm, dividing by simple binary fission and achieving full length before next division, not in meristematic zones, 3.2–7.5 μm long. Apical cells cylindrical with rounded apices, not different in length or morphology from internal cells.','Akagha et al. 2019',NULL,0,0),(1386,1650,'description','Colony with sinuous, wavy fascicles of filaments, spreading from center, olive green in color. Filaments with single trichomes without sheath in young cultures and hormogonia (Fig. 1A), later with one to two trichomes in a common sheath (Fig. 1. B and C), soon after forming two trichomes in a sheath the sheath ruptures and the filament forms pseudobranches (Fig. 1D), also forming tight loops within a common filament, which break to form geminate pseudobranches. Sheath colorless, soft, thin. Trichomes sometimes twisted within the sheath, slightly constricted at the crosswalls, with meristematic zones, with necridia, up to 3 μm wide. Cells shorter than wide to isodiametric, occasionally longer than wide when stressed, with chromoplasm distinct from centroplasm (i.e., evident parietal thylakoids). Apical cells rounded to conical, sometimes forming irregularly shaped involution cells (Fig. 1B). Hormogonia may be widened at one end, tapering towards the more actively growing opposite end (Figs. 2, C and R, 3C). Following transfer to fresh, nutrient-replete media trichomes lack sheath material and terminal slime caps; in senescent cultures with well-developed sheath present, with a broadened terminal or subterminal slime cap (Fig. 1, B and C). Calyptra never present.','Pietrasiak et al. 2019',NULL,0,0),(1387,1651,'diagnosis','Morphologically very similar to M. californica, differing only in the infrequent presence of involution cells and the prominent slime cap in mature cultures; molecularly differing in consistent sequence divergence in Helix 21 of the 16S rRNA molecule (Fig. 4).','Pietrasiak et al. 2019',NULL,0,0),(1388,1651,'description','Filaments consisting of sheathless trichomes early in life cycle, possessing one to two trichomes in a common sheath when mature, (1.6)–2–3.2 μm wide. Trichomes slightly constricted at the crosswalls, 1.6–3.0 μm wide. Cells at first ungranulated, developing polyphosphate bodies at 4 weeks, which dissipate with maturation of the population, 1–3 μm long. Apical cells up to 5.4 μm long. Involution cells slightly widened, inconspicuous, rare. Terminal slime cap extending outward from the apical cells 1.2–1.4 μm.','Pietrasiak et al. 2019',NULL,0,0),(1389,1652,'diagnosis','Morphologically very similar to M. chilensis, differing only in the frequent presence of prominent involution cells, longer vegetative cells, and presence of an inconspicuous slime cap in mature cultures; molecularly differing in consistent sequence divergence in Helix 21 of the 16S rRNA molecule (Fig. 4).','Pietrasiak et al. 2019',NULL,0,0),(1390,1652,'description','Filaments consisting of sheathless trichomes early in life cycle, with one to two trichomes in a common sheath when mature, 1.6–3.6 μm wide. Trichomes slightly constricted at the crosswalls, 1.6–3.2–(3.4) μm wide. Cells at first ungranulated, developing polyphosphate bodies at 4 weeks, which dissipate with maturation of the population, 1.2–5 μm long. Apical cells up to 4.0 μm long. Involution cells distinctly widened, conspicuous, common, up to 4 μm wide. Terminal slime cap extending outward from the apical cells 1.0 μm.','Pietrasiak et al. 2019',NULL,0,0),(1391,1653,'description','Filaments densely and irregularly entangled, forming compact colony (thallus), attached to the substrate, pinkish to reddish or brownish-red; unbranched, straight to curved, not attenuated toward the ends. Sheaths colorless, firm, thin, and slightly to rarely distinct. Trichomes 0.8–2.9 um wide, immotile, slightly constricted to strongly constricted at the cross walls. Cells isodiametric, longer or shorter than wide with peripheral thylakoids; apical cells rounded or conical rounded.','Konstantinou et al. 2019',NULL,0,0),(1392,1654,'description','Filaments with a single trichome per sheath, unbranched, straight to curved, densely, and irregularly entangled and joined in clusters. Sheaths colorless, firm, thin, and slightly distinct. Trichomes cylindrical, slightly constricted at the cross walls, not attenuated toward the ends. Trichomes appear reddish and do not exhibit gliding movement. Hormogonia formation common. Cells typically barrel shaped, shorter than wide to isodiametric, 0.76–1.65 um in length and 0.97–1.8 um in width. Cell contents homogenous. Thylakoids (three to four) arranged peripherally. End cells rounded.','Konstantinou et al. 2019',NULL,0,0),(1393,1655,'description','Filaments with a single trichome per sheath, unbranched, curved or wavy, occasionally irregularly spirally or screw-like coiled, and irregularly entangled and joined in clusters. Sheaths colorless, firm, and thin. Trichomes cylindrical and slightly constricted to strongly constricted at the cross walls. Trichomes pinkish to pale purple, not attenuated toward the ends. Hormogonia formation common. Cells longer than wide, 1.02–1.91 um in length and 0.7–1.08 um in width. Cell contents homogenous. Thylakoids (three to four) arranged peripherally. End cells rounded.','Konstantinou et al. 2019',NULL,0,0),(1394,1656,'description','Filaments with a single trichome per sheath, unbranched, straight to curved, and irregularly entangled and joined in clusters. Sheaths colorless, firm, and thin. Trichomes cylindrical and constricted to strongly constricted at the cross walls. Trichomes pinkish, not attenuated toward the ends. Hormogonia formation common. Cells longer than wide, 1.36–2.76 um in length and 0.84–1.97 um in width. Cell contents homogenous. Thylakoids<br>(three to four) arranged peripherally. End cells rounded.','Konstantinou et al. 2019',NULL,0,0),(1395,1522,'description','Lager schwärzlich -blaugrün. Trichome gerade oder wenig gebogen, an den Scheidewänden deutlich eingeschnürt, am Ende wenig verjüngt, 1,8—2 um breit, lebhaft blaugrün. Scheiden dünn, &nbsp;fest, hyalin, durch Chlorzinkjod nicht blau gefärbt. Zellen fast quadratisch, etwas länger oder etwas kürzer als breit, 1,2—3 um lang, an den Scheidewänden nicht granuliert. Endzelle stumpf kegelförmig.','Lemmermann 1907',NULL,0,0),(1396,1658,'description','Filamtents forming a thin, compact, pale-purplish stratun; trichomes 1.2-1.5 um diam., pale purplish, not constricted; cells qundrate to one-half as long as the diameter, homogeneous; cross walls dostinct; apical cells blunt.','Gardner 1927',NULL,0,0),(1397,1660,'description','Strato indefinito tenui, expanso, gelatinoso; trichomatibus brevibus, leviter flexuosis, moniliformibus, 2.4-2.7 um diam.; vaginis hyalinis, amplis, gelatinosis, diffluentibus; cellulis quadratis aut subquadratis, maxime ad dissepimenta constrictis, cellula apicali majori, subsphaerica, membrana superne non incrassata.&nbsp;','Setchell et Gardner in Gardner 1918',NULL,0,0),(1398,1662,'diagnosis','Stratum expansum vel flocculosum, aerugineum aut nigro-viride. Filia recta aut subflexuosa, laxa intricata. Vaginae tenue et firmae. Trichomata ad genicula non constricta, apice recta non attenuata. Cellula apicalis rotundata, calyptra nulla. Articuli diametro trichomatis longiores, 1.05-2.45 um crassi et 3.8-12.0 um longi.','Campbell 1985',NULL,0,0),(1399,1662,'description','Thallus benthic to pseudo-planktic (suspended); stratiform to flocculent; composed of loosely woven (unbranched) filaments and motile trichomes which form and then abandon their sheaths. Sheaths are thin and firm. Thallus and trichome coloration varies from pale grayish to dark blue-green. Trichomes are straight or slightly &nbsp;bent, not constricted at the crosswalls, usually several hundred microns long. The trichome end does not taper. The end cells is rounded. There is no thickening of the endcell wall and no calyptra. Cells may contain granulation which is ± evenly distributed. Sulphur granules often adhere to the outside of trichomes in the hypolimnion. Cell width is 1.05-2.45 um; cell length 3.8-12.0 um in nature and in culture. The organism is halophilic and polyeuryhaline.','Campbell 1985',NULL,0,0),(1400,707,'description','Colony on agar dark green or brown, amorphous. Filaments usually very long with basal heterocyte, swollen at the base, then gradually tapering towards the end, without terminal hair, often with false branching, single or double. Sheath 0.5–1.5 μm thick, unstructured, colorless. Trichomes notably constricted at cross-walls, 7–9 μm wide at the base and 3.0–4.3 μm wide at well-developed ends. Cells olive green, brown to violet, cylindrical or barrel shaped, shorter or longer than wide, 3–8 μm long, basal:apical ratio 1.8–2. Terminal cell longer than wide, cylindrical or bluntly conical. Heterocytes basal or intercalary, green to yellowish, hemispherical or cylindrical, rarely conical, 4–7 μm wide, 4–8 μm long. Reproduction by hormogonia with almost spherical cells. No akinetes were observed.','Hauer et al. 2013',NULL,0,0),(1401,762,'description','The life cycle contains several morphologically distinct stages (Fig. 1). One was described above, i.e long, gradually tapering, heteropolar filaments (Figs 1A, B, P). The second consists of hormogonia composed of short, isodiametric, barrel-shaped to spherical cells resembling in morphology Nostoc Vaucher ex Bornet et Flahault (1888: 181) types lacking the sheath (Fig. 1E). Some cells within the hormogonia grow in size and change their shape to spherical (Figs 1D, O). Cells may sometimes divide in more than one plane (Figs 1L, M, O), but never form a true branch. A new filament then germinates from the hormogonia (Fig. 1C). The first cell of the filament becomes a heterocyte. The hormogonia with large spherical cells (e.g. Fig. 1D) occur in young cultures only.<br>Our strain differs from the morphologically similar genus Calothrix Agardh ex Bornet et Flahault (1886: 345) by the absence of a terminal hair and frequent false single or double branching (Figs 1G, H, N). As notable from Fig. 2, the 16S rRNA sequence of Calochaete cimrmanii is very distant from members of Rivulariaceae and is more related to Microchaetaceae. The most similar are sequences of Tolypothix strains UAM 332, 334, 337 and PCC 7504, but the degree of tapering is significantly lower in these strains. The low degree of tapering itself is one of the key diacritical features of the genus Tolypothrix Kützing ex Bornet et Flahault (1887: 118), which is accepted in both the botanical (Komárek &amp; Anagnostidis 1989) and bacteriological (Castenholz 2001) literatures. From the above mentioned Tolypothrix strains, Calochaete cimrmanii differs also by living in a significantly different –non-aquatic, high mountain– habitat.','Hauer et al. 2013',NULL,0,0),(1402,1668,'description','Fila plus minusve regulariter spiralia, passim recta. Vaginae tenues, hyalinae. Trichomata circiter 2 um crassa; articuli diametro trichomatis breviores aut longiores, 1,2 um ad 3 um longi ; dissepimenla binis granulis protoplasmaticis notala? (praeparationem microscopicam vidi).','Gomont 1892',NULL,0,0),(1403,1671,'description','Stratum laete aerugineum, luteolum necnon lateritium, tenue, membranaceum, valde expansum. Fila flexuosa, dense intricata. Vaginae arctae, papyraceae, mucosae, vel in mucum amorphum omnino diffluentes, chlorozincico iodurato caerulescenles. Trichomata laete caruginosa, ad genicula haud constricta, apice recta breviler attenuata non capitata , 1 um ad 1.5 um crassa ; articuli diametro trichomatis longiores, 2 um ad 4 um longi; dissepimenta quaternis granulis protoplasmaticis notata, plerumque inconspicua ; cellula apicalis acute conica; calyptra nulla (v. s.).','Gomont 1892',NULL,0,0),(1404,669,'description','Filaments solitary, in clusters or forming mats, 0.8–4 lm wide, without heterocytes andakinetes, with thin sheaths, with false branching of both tolypotrichoid and scytonematoid types. Trichomes cylindrical,<br>not or slightly attenuated towards the ends, not or slightly constricted at cross-walls. Cells isodiametric or<br>slightly shorter or longer than wide, with thin cross-walls, without gas vesicles, heterocytes and akinetes. Arrangement of thylakoids is parietal with facultative circular formations. Reproduction by fragmentation of trichomes and hormocytes (immotile hormogonia).','Taton et al. 2011',NULL,0,0),(1405,670,'description','Filaments solitary or in small, free clusters, thin, slightly or irregularly coiled, longer filaments with obligatory false branching (in nature). Trichomes are cylindrical, pale greyish or blue-green, not or slightly constricted at cross-walls, but visible in OM as constricted at cross-walls (compare photos from OM with EM), not attenuated towards the ends, 1–2.5(3) um wide. Cells cylindrical with homogeneous content, ± isodiametric or slightly longer or shorter than wide, but with almost invisible cross-walls in LM without staining; end cells rounded without calyptra. Sheaths very thin, colourless, attached or slightly widened from trichomes, diffluent. False branching obligatory, branches solitary or in pairs.','Taton et al. 2011',NULL,0,0),(1406,630,'eco_distro','','Sciuto et &nbsp;al. 2017',NULL,0,1),(1407,1675,'description','Fäden einzeln oder zu mehreren zwischen anderen Algen, unregelmäzig gekrümmt. &nbsp;Zellen etwa 1 um breit, &nbsp;etwa &nbsp;doppelt so lang. An den Scheidewanden &nbsp;eingeschnürt. Farbe blass-blaugrün. Endzelle &nbsp;abgerundet. Die Fadenenden &nbsp;stehen oft weit aus &nbsp;den farblosen &nbsp;Scheiden hervor, &nbsp;Nach Färbung (etwa mit Gentianaviolett) besonders in den älteren Scheidenteilen &nbsp;trichterförmige Trichomstücke sichtbar. Mit Blutlaugensalz und Salzsäure keine Eissnreaktion.','Krieger 1944',NULL,0,0),(1408,630,'eco_distro','Distributed in mountain and polar environments; occurring in freshwater and subaerophytic habitats, such as wet soils and wet rock surfaces.','Sciuto et al. 2017',NULL,0,0),(1409,765,'description','Thallus green to dark green forming small moss-like strata. Young filaments isopolar, bent in the middle. Older filaments heteropolar and pseudobranched, with basal heterocysts and rarely with intercalary heterocysts. Heteropolar filaments (10) 12–18 um wide (12.3±1.2 mm, n=30), isopolar filaments 10–14 um (10.6±1.3 um, n=30). Cells shorter than wide, 6–9 um wide, 2–5 um long. Reproduction by hormogonia. Akinetes present.','Lamprinou et al. 2012',NULL,0,0),(1410,1681,'diagnosis','Filis solitariis; rectis vel vix curvatis, tenuissimis; vaginis hyalinis, tenuissimis; trichomatibus pallide aerugineis, ad genicula non constrictis, apice non attenuatis, 0,8-l,6 um crassis; articulis subquadratis ant diametro duplo longioribus, 1,6-3,2 um longis; contentu homogeneo, sed dissipimentis 2—4 granulis pallidis notatis; dissipinientis pellucidis; cellula apicali rotundata; calyptra nulla.&nbsp;','Schmidt 1914',NULL,0,0),(1411,1683,'description','Filaments mesurant 2 à 2 1/4 um de diamètre à gaine nette incolore. Trichome formé de cellules arrondies, un peu oblongues, allongées dans le sens de la longueur du filament, à contenu homogène, vert-bleu. Les cellules sont séparées les unes des autres, leur écartement atteint parfois la longueur même des cellules qui mesurent 1,5 à 2 um de long et 1 à 1,5 um de large','Kufferath 1929',NULL,0,0),(1412,1685,'description','Plants forming a thin stratum with the filaments intricately interwoven and tortuous and with distinct sheaths more or less diffluent: trichomes aeruginous, constricted at the cross-walls, finely granular, 2-2.3 um diam., with cells 1.5-2.5 times as long as the diameter; apical cell straight, blunt, rounded, and wall not thickened.','Gardner 1932',NULL,0,0),(1413,1688,'description','Trichomes 1-1.5 um diam.; sheaths distinct, more or less confluent when denselly aggregated, pale rose-pink in color.','Gardner 1927',NULL,0,0),(1414,1697,'description','Filaments 7.2-7.8 um diam., long, straight, or arcuate and smooth; trichome 2.5-3 um diam., not constricted at the dissepiments, neither uncinate nor capitate; cells 2-2.5 times as long as the diameter, contents homogeneous, walls inconspicuous; apical cells rounded; end wall not thiekened perceptbly more than the others; color pale aaruginous; sheath relatively thick, more or less gelatinous, hyaline, homogeneous.','Gardner 1927',NULL,0,0),(1415,1105,'description','Colonies caespitose on rocks in the marine habitat, formed by filaments arranged in erect fascicles, with heteropolar appearance achieved after basal fragmentation. Sheaths lamellate, thin or wide, becoming diffluent at the end, colorless or yellow–brown, and roundly closed or open at the end. Trichomes are untapered or distinctly tapered at some phase of life–cycle and/or in culture material, sometimes developing a hyaline or semi–hyaline hair, vacuolated or not; with geminate and single false branches, mainly in basal parts of filaments. Trichomes constricted or not at cross walls, in both environmental samples and strains. Cells of variable length and shape, shorter than wide to almost isodiametric in environmental and culture material. Heterocytes are basal or intercalary, solitary or serial (–3), of variable length and shape. Hormogonia, isopolar or heteropolar, produced through trichome fragmentation, with or without necridic cells, cell constriction or heterocyte breakup. Akinetes unobserved.','González-REsendiz et al. 2019',NULL,0,0),(1416,1106,'description','Thallus caespitose, composed of blackish–green erect filaments densely fasciculate (Figs 1A–1B, 3A), 2–3 cm high, filaments with rare geminate false branching, 9–15 μm wide (Fig. 1C). Sheaths firm, cylindrical, stratified, yellowish brown (Figs 1C, 1G–1H, 2B, 4A) Trichomes cylindrical, constricted or not at cross–walls, 6–10 μm wide (Figs 1H, 1J, 1K); slightly tapered towards the ends as well as in hormogonia (Figs 2K, 4A); apical cell colorless, distinctively short and spherical–rounded, bead–like (Figs 1D–1G, 5D–5E). Cells with blue–green to olive–green granulated content (Fig. 1K), isodiametric in old filaments, 5 to 8 μm long, shorter than wide in apical zones, 2–3 μm long 5.6–7 wide. Heterocytes intercalary, elongated, flattened, discoid or cylindrical 8–15 μm long, up to 2 to 3 times longer than wide, 4.5–6.7 μm long, 1.8–4.8 μm wide, rarely three short heterocytes contiguous or near one another (Figs 1H–J, 2A–2B). Reproduction by isopolar hormogonia attached to filaments, straight or more frequently crescent–shaped (Figs 2G–2J, 3B, 3D–3F, 4C, 5C, 5G, 5I). Hormogonia, produced by necridic cell or heterocytes formation (Figs 2B–2G, 5H) Akinetes not observed in environmental or culture conditions. Transmission electron microscopy (TEM) images obtained from Nunduva fasciculata field material show thylakoids disposed in packets (Fig. 4B) with isopolar hormogonia with bead–like terminal cell<br>(Fig. 4C).','González-Resendiz et al. 2019',NULL,0,0),(1417,1107,'description','Thallus filamentous, heteropolar and isopolar (6B, 6D, 6F–6H), with frequent geminate false branching (6A, 6D, 6F). Sheaths diffluent, lamellate, colorless, open at the end. Trichomes constricted at cross walls, 1.7–2.6 μm long, 7.5–9 μm wide, tapered to form long hair composed by semi–hyaline and “vacuolated” cells up to 1–1.5 μm wide (6A, 6E–6F). Cells with olive–green granulated content, 2 to 5 μm long, wider than long; in the apical zone cells are longer than wide, 1.7–2.8 μm long, 1.2–1.5 μm wide. Heterocytes basal and no more than one, conical or hemispherical in shape (4.9–5.4 μm wide 2.5–2.6 μm long) (6F–6H). Reproduction by heteropolar and isopolar hormogonia, produced by separation of branches and by deep cell constriction without necridic cell (Figs 6B–6D, 6E, 6H–6J arrows). Akinetes not observed in culture conditions.','González-Resendiz et al. 2018',NULL,0,0),(1418,1115,'description','Thallus caespitose, composed of yellowish–brown erect heteropolar filaments, 3–8 μm wide (Fig. 7A), with rare single false branching. Sheaths diffluent, lamellate, colorless to yellowish, and flared at the apex (Figs 7B–7D, 8B, 8L–8O arrows). Trichomes cylindrical, constricted or not at cross–walls, 2–7 μm wide, slightly swollen at base and tapered without hair (Figs 7A, 7D–7E, 7H, 8A, 8–8F, 8L–8O). Cells shorter than wide, with olive–green granulated content, 1–2.7 μm long in basal zone; 0.5–0.8 μm long in apical zone. Heterocytes intercalary or basal, elongated, discoid or cylindrical, 4–4.5 μm, long 4–6 μm wide, rarely two short heterocytes contiguous or near one another (Figs 7B–7C, 7F–7G, 8D arrow). Reproduction by isopolar hormogonia that may remain temporarily within the sheaths (Fig. 7H), or heteropolar hormogonia produced by cell constriction, or heterocyte formation and by separation of branches (Figs 8F, 8L, 8J, 8O arrows). Akinetes not observed in environmental or culture conditions.','González-Resendiz et al. 2018',NULL,0,0),(1419,1116,'description','Young cultures with heteropolar filaments, straight or wavy, taper towards the end, 5–11 um wide, with thin, colorless unstratified sheath, with geminate false branching (Fig. 9A). Trichomes 5–9 um wide, clearly constricted at cross walls, swollen at basal part, without a terminal hair (Figs 9B–9D). Cells distinctly shorter than wide. Heterocytes basal, sometimes in pairs, hemispherical or trapezoid, up to 10 um wide. Reproduction by trichome disintegration. Old cultures with heteropolar or isopolar filaments (Fig. 9G), straight or wavy, not tapering towards the end, 5–13 um wide, with colorless sheath, up to 4 um thick, stratified, frayed when old (Figs 9E–9F, 9J). Trichomes 5–9 um wide, width slightly varying along the length of trichome. Cells distinctly shorter than wide up to isodiametric, well developed terminal cell almost spherical (Figs 9H, 9I, 9G). Heterocytes basal and intercalary, cylindrical (Figs 9I–9J). Reproduction by isopolar hormogonia (Fig. 9K) and by trichome disintegration. Akinetes not observed.','González-Resendiz et al. 2018',NULL,0,0),(1420,1121,'description','Filamentous, solitary, or many together forming a caespitose, woolly thallus, olive-green to blackish green in color. Filaments straight to variously flexuous, sometimes slightly coiled, cylindrical, with solitary or geminate false-branching, initiated following the formation of necridic cells; sheath firm, lamellated, with a smooth exterior surface, colorless or yellowish-brown in mature filaments. Trichomes isopolar, not or slightly constricted at the cross walls. Vegetative cells discoid to short barrel-shaped, blue-green in color; apical cells widely rounded. Heterocytes intercalary, discoid to subspherical, single or up to two in series. Reproduction by hormogonia,<br>which develop at the ends of branches and liberate from the sheaths. Akinetes absent.','Sendal &amp; McGregor 2018',NULL,0,0),(1421,1700,'description','Thallus macroscopic, caespitose, cushion like, dull-brown to blackish-green. Sheaths thin, firm, colorless, yellow or yellowbrown. Mature filaments polyseriate, heteropolar, 41.3–77.1 μm (=57.8μm) wide, richly branched at the base. Branches T-type and narrower than the main filament, 14.4–50.2 μm (=34.8 μm) wide, with long, broadly developed lateral branches or with short mammilliform hormogonia. Hormogonia short, uniseriate, arising on both sides, 13.2–27.9 μm (=19.6 μm) wide and 35.2–59.2 μm (=45.8 μm) long. Cells spherical, 8.2–18.3 μm (=12.6cμm) wide and 8.8–18.5 μm (=13.1μm) long, in older parts regularly barrel-shaped. Heterocytes mostly lateral, nearly spherical, 6.2–13.8 μm (=9.2 μm) wide and 6.2–12.9 μm (=8.5μm) long. Akinetes not observed.','Song et al. 2015',NULL,0,0),(1422,1702,'description','Filaments much contorted and geniculate, 3.6-4 um diam., branching sparse ; trichomes 1.5-1.8 um diam., slightly constricted at the cross-walls, not attenuated at the apices; cells pale aeruginous, quadrate to 2 times as long as the diameter; apical cell blunt.','Gardner 1927',NULL,0,0),(1423,566,'diagnosis','Proprietatibus descriptis pro genere sed differt characteribus sequentibus: filamentis distincte complanatis e cellulis aliquot centum cylindricis 1.2–2.4 um longis 1.1–1.5 um diametro compositis; nodulis discretis compactis forma ac amplitudine variabilis secus filamenta dispositis, parte filamenti in collationem arctum plicata et per vaginam distinctam omnino circumcincta constantibus; reproductione per fractione trichomatum ad situs cellularum necroticarum; et hormogonia motibus tremulis.','Li et Brand 2007',NULL,0,0),(1424,566,'etymology','Specific epithet is the Latin name for ‘little knot’ or ‘nodule’, a characterization of the distinguishing feature of this organism.','Li et Brand 2007',NULL,0,0),(1425,1710,'description','Stratum crustaceum fuscum vel fusco-viride, siccitate subdurum, sine contritione haud dissolvendum. Fila vix elongata, tortuosa, abundanter pseudo-ramosa, pseudo-ramis plerumque geminatis, patentibus, brevibus, filo primario aequicrassis. Vaginae haud attenuate, initio laeves, hyalinae, demum crassae, erosae, luteofuscae, chlorozincico iodurato haud caerulescentes. Trichomata dilute aeruginea, torulosa, submoniliformia, &nbsp;1,5-2 um crassa, breviarticulata, articulis diametro ad duplo brevioribus; cellula apicalis rotundata (v. s.).','Gomont 1899',NULL,0,0),(1426,1216,'description','Colony compact, olive-brown, soft to hard, dry, in clumps or small irregular mounds, arising from the substrate with extensions that are higher than wide, consisting of aggregates of coccoid cells, in diads or tetrads, but not forming large cubical sarcinoid clusters, containing pseudofilamentous, pseudodichotomously branching aggregates, united laterally by the confluence of thin gelatinous sheaths. Sheaths colorless, thin, scarcely apparent, later, in the older stages, more robust with yellowish-orange color. Pseudofilaments uni- or biseriate, 5–12.5 μm wide, with rounded end cells lighter in color than central cells, 4–10 μm wide, 3.5–22 μm long. Cells of the central portion of the thallus irregular, with binary to multiple fission, but mainly sarcinoid, dark olive-green, brown, to brownish orange in older parts of colony, nongranular, with reticulate nature of the cytoplasm often evident, 2.5–10 μm wide, up to 11.5 μm long. Baeocytes uncommon, 1.4–2.8 μm in diameter.','Shalygin et al. 2019',NULL,0,0),(1427,1715,'description','Fila gracilia, elongata, subrecta, initia crebre, aeate provecta parce pseudo-ramosa, pseudo-ramis solitaiis aut geminatis. &nbsp;Vaginae hyalinae, &nbsp;tenuissimae, cylindeaceae, chlorozincico iodurato non caerulescentes. Trichomata pallide luteo-viridia, ad genicula constricta, 1 ad 1,5 um crassa; articuli diametro longiores, 2 ad 2,5 um longi; dissepimenta non granulata; cellula apicalis rotundata.','Gomont 1892',NULL,0,0),(1428,1717,'description','Fäden 1.72-2 um breit, vielfach gebogen, locker, kein Lager bildend, blaugrün, selten verzweigt. Zweige einzeln abgehend, Scheiden hyalin, dünn. Die Farbe der Tricheme sehr dilut, Scheidewände schwer sichtbar. Zellen <br>viereckig, meist zweimal so lang als breit. Jederseits liegt an der Scheidewand eine sehr grosse protoplasmatische Granel. Endzelle abgerundet. Oft ist die grosse Protoplasmagranel in zwei kleinere aufgelöst.&nbsp;','Schmidle in Simmer 1901',NULL,0,0),(1429,1719,'description','Fila tenuissima, in stralum luteo-ochraceum intricata, plus minusve curvata, fragilia. Vaginae initio tenues, hyalinae, demum crassae et ochraceae, chlorozincico iodurato non caerulescentes. Trichomata aeruginea, frequenter interrupta, eximie torulosa, 0,9 um crassa; articuli diametro trichomatis breviores, 0,6 ad 0,8 um longi; dissepimenta haud granulata; cellula apicalis rotundata; calyptra nulla.','Thuret ex Gomont 1892',NULL,0,0),(1430,1723,'description','Lager dünn, hautartig, olivenbraun gefärbt. Fäden gekrümmt, locker verflochten, 1 bis 1.8 um dick, oft undeutlich gegliedert. Veget. Zellen fast ebenso lang wie breit, mit oliven- oder gelblich grünem Inhalte. Scheiden dünn, eng anliegend.','Kützing ex Hansgirg 1892',NULL,0,0),(1431,1725,'description','P. strato tenuissimo, pallida aerugineo; filis subrectis vel leviter flexuosis, angustissimis, plus minusve intricatis; vaginis hyalinis, arctissimis, delicatissimis et non mucosis; trichomatibus laete aerugineis, angustissimis, ad dissepimenta non constrictis, apicibus rectis et non capitatis; cellulis diametro 3 1/4- 4 1/2 plo longioribus, &nbsp;protoplasmate homogeneo. Crass, trich. 1,6-1,8 um.&nbsp;','West 1902',NULL,0,0),(1432,1729,'description','Lager epiphytisch auf &nbsp;Meeresalgen sitzend. Fäden den Scheiden 1,5-2 um breit. Zellen fast quadratisch oder cylindrisch, 2-7 um lang. Scheiden sehr dünn, schwer zu unterscheiden.','Lemmermann 1899',NULL,0,0),(1433,791,'description','Thallus macroscopic, blackish–violet mats, densely fasciculated and prostrate on substrate. Mature filaments isopolar, cylindrical, 17.5 – 24.5 μm wide ( x= 21 μm), closed at rounded ends, open after hormogonia are released. Sheaths thin, not lamellated when young, slightly lamellated with age, colorless. Mature trichomes 12.5 – 20 μm wide ( x= 7 μm), not attenuated, not or slightly constricted, generally of same width along the whole length, becoming wider at the ends when forming hormogonia; sometimes calyptras are found in apical cells. Young trichomes attenuated in single or both ends. False branching rare, predominantly double, although sometimes single, or in some filaments growing from an attached hormogonium. Cells violet to brown, variable in length, shortest in hormogonia, apical cells and meristematic zones; longer in older parts, 5.25 – 18.7 μm in length ( x= 11.4 μm), with granular content mainly in older cells; vacuole– like structures were found in rows of neighboring cells. Heterocytes solitary, intercalar, discoidal to rectangular, wider than long in trichomes 12.48 –16.4 μm wide ( = 14.85 μm) by 7.4 – 15.6 μm long ( x= 9.6 μm); solitary, basal, hemispherical in hormogonia. Hormogonia with asymmetrical growth becoming heteropolar, wider than trichomes 16.2 – 41.5 μm wide (x = 23 μm).','Becerra-Absalón et al. 2013',NULL,0,0),(1434,769,'description','Thallus is expanded, partially endolithic. Creeps on the substrata, sometimes interwoven with other cyanobacteria. Trichomes are uniseriate, surrounded by a mucilaginous sheath, embedded with calcareous deposits at the base. Trichomes are irregularly branched, at the tips (true V-branching) and laterally (true T-branching). Cells are cylindrical or torulose, 4.5–6.5 mm long and violet. Heterocysts are intercalary. Reproduces by hormocysts. A ring of mucilaginous material helps separation.','Lamprinou et al. 2011',NULL,0,0),(1435,693,'description','Freshwater; thallus a prostrate, greenish blue-black woolly mat of densely aggregated filaments. Filaments straight to variously contorted, facultatively and infrequently pseudobranched. Sheath colorless, hyaline, when old distinctly lamellated (roughened) and colored, open at the apex. Trichomes isopolar, uniformly cylindrical, up<br>to 70 lm wide; not or slightly constricted at the cross-walls. Cells discoid, 5–159 broader than long; contents finely granular, without aerotopes; apical cells rounded, without a calyptra or thickened outer cell wall. Reproduction by motile hormogonia formed by necridia.','McGregor &amp; Sendall 2015',NULL,0,0),(1436,1737,'diagnosis','Filis rectis aut arcuatis, solitariis aut in fasciculos parvos aggregatis, ad 200 um longis; vaginis tenuissimis, hyalinis, arctis, papyraceis, chlorozincico iodurato non caerulescentibus; trichomatïbus pallide aerugineis aut violaceis, ad genicula constrictis, 2 um circiter crassis, apice non attenuatis; articulis diametro duplo aut triplo breviorïbus, contentu homogeneo; dissepimentis pellucidis, non granulatis; cellula apicali superne convexa, vix attenuata, non capitata (v. in form.).','Frémy 1930',NULL,0,0),(1437,1122,'description','Heterocystous, uniseriate, filamentous, with obligatory false branching. Thallus prostrate, forming flat or woolly mats, sometimes occurring as solitary filaments amongst other algae. Trichomes monoseriate, isopolar, cylindrical. Sheaths usually thick, firm or gelatinous, often lamellated, colorless or variously colored. Heterocytes intercalary, occurring singly or in pairs. Akinetes absent. Reproduction by the formation of hormogonia.','Sendall &amp; McGregor 2018',NULL,0,0),(1438,1181,'description','Filamentous cyanobacterium with heteropolar thallus. Filaments creeping or attached to the substrate, solitary or in small groups, but not in distinct colonies, with rare false branching. Sheath firm, attached to the trichome, colorless, yellow-brown or brown, homogenous or slightly layered in older filaments, sometimes open at the end. Trichomes widened at the base, with at first one basal heterocyte, later developing a larger heterocyte above the first heterocyte, and finally with a single large heterocyte when the original heterocyte is shed, constricted at the cross walls,  +-continuously narrowed toward the apex, with most species being able to produce a long hyaline or semi-hyaline hair. Akinetes not observed. Reproduction by necridic cells and by separation of secondary branches. D1–D10 helix of the 16S–23S ITS region with a subapical unilateral bulge of six nucleotides (typical sequence 5-GGUAAU-30) on the 30 side of the helix in all ribosomal operons.','Berrendero et al. 2016',NULL,0,0),(1439,1184,'description','Thallus filamentous, heteropolar. Sheath firm, attached to the trichome, yellow-brown, colorless at the apical part of trichome, homogenous or slightly layered in older filaments, sometimes opened at the end (Fig. 1, A and F). Trichomes constricted at the cross walls (Fig. 1, C and E), with vegetative cells at the base of filament (7) 8–10 (13) um wide by (4) 5–6 (8) um long, with cells in the middle part of filaments (5.5) 6–7 um wide by (3.5) 4–5.5 (6) um long (Fig. 1, A, C, E, F), ending in hyaline or semi-hyaline hairs (Fig. 1, B, D, G) composed of up to 50 cylindrical cells, not constricted or constricted at the cell walls, 1.5–3 lm wide by 3–7 (10) um long. Chromatoplasma and pale centroplasma clearly differentiated (Fig. 1C). Heterocytes rarely occurring in intercalary position, mostly basal, one or two (especially in developed filaments), with most basal heterocyte smaller, conical or hemispherical, 4–6 um long and 5–7 um wide, with second, sub-basal heterocyte hemispherical, (5) 6–11 (13) um wide by (3) 5–9 (10) um long (Fig. 1, A, C, E–G).','Berrendero et al. 2016',NULL,0,0),(1440,1185,'description','Thallus filamentous, heteropolar. Sheath firm, attached to the trichome, yellow-brown, colorless at the apical part of trichome, homogenous or slightly layered in older filaments, sometimes opened at the end (Fig. 3C). Trichomes slightly constricted or constricted at the cross walls, with vegetative cells at the base of filament 6–10 um wide by 4–6 (8) um long, with cells in the middle part of filaments 3–5 um wide by 3–5 (6) um long, ending in very long hyaline or semi-hyaline hairs composed of up to 80 cylindrical cells, not constricted or constricted at the cell walls, with hair cells 1.5–2 um wide by 4–5 (8) um long (Fig. 3F). Chromatoplasma and pale centroplasma clearly differentiated. Heterocytes rarely occurring in intercalary position, mostly basal, one (Fig. 3, D and E), rarely two, the first heterocyte being shed soon after formation of the second heterocyte. Before the initial basal heterocyte is lost, it is hemispherical, 3–4 (5) um wide by (5) 6–7 lm long, with second, subbasal heterocyte hemispherical, 6–7 (8.5) um wide by 4–5 um long (Fig. 3, A and B).&nbsp;','Berrendero et al. 2016',NULL,0,0),(1441,1182,'description','Thallus filamentous, heteropolar. Sheath firm, attached to the trichome, yellow-brown, colorless at the apical part of trichome, homogenous or slightly layered in older filaments, widened and closed at the end (Fig. 4E). Trichomes green, constricted at the cross walls, with vegetative cells at the base of filament 10–15 um wide by 5–6 (8) um long, with cells in the middle part of filaments 7–8 um wide by (3.5) 4–5 (6) um long. Trichome ending in a distinct, tan-colored tapered or conical cell, 4–7 (9) um wide and 5–13 lm long (Fig. 4, A, B, F). Two to five penultimate cells are often rounded or oval, 8–9 um wide and (4) 6–8 um long (Fig. 4, A and F). Hyaline hairs were not observed. Chromatoplasma and pale centroplasma clearly differentiated. Basal heterocytes one (Fig. 4C), rarely two (Fig. 4, B and G). Before the initial basal heterocyte is lost, it is hemispherical, 6.5–7.5 um wide by (3.5)4–6.5 um long, with second, sub-basal heterocyte hemispherical, (6) 7–9.5 um wide by 4–6 um long (Fig. 4, A and B). Heterocyte occurs in intercalary position as well (Fig. 4, C and D.), with hormogonia production often starting adjacent to heterocytes (Fig. 4D).','Berrendero et al. 2016',NULL,0,0),(1442,1741,'diagnosis','Differing ecologically from all described species by occurrence in hypersaline evaporation lake. Similar to calcified species <em>R. haematites</em>, <em>R. dura</em> and <em>R. rufescens</em>, but having basal cells distinctly shorter than wide with greater maximal width. Also similar to <em>R. biasolettiana</em>, from which it differs by presence of granules inside the cells, presence of slime pads, branching pattern and geographic distribution (Table 1).','Shalygin et al. 2018',NULL,0,0),(1443,1741,'description','In the natural environment, blackish macroscopic colonies compact, irregular-spherical to hemispherical, &nbsp;sometimes pillow-like, attached to the substrate, establishing microbial communities with eukaryotic algae and heterotrophic bacteria, often encrusted and surficially whitened with calcium carbonate, up to several cm. Filaments initially short, long in older stages, both commonly singly and geminately branched, with young isopolar Tapinothrix clintonii-like forms with trichomes tapered towards both ends, usually attached to the long, lamellated main filaments, maximally 500 μm long. Young filaments isopolar or heteropolar, sometimes with geminate branches, rarely aggregated into star-like fascicles (up to 20 μm in diameter), occasionally attached to long main filaments. Sheaths firm, attached to trichomes or widened, usually intensely lamellated, sometimes with perpendicular striations near branches, rarely swollen, usually colourless, yellowish when old or slightly violet, up to 35 μm wide. Mucilaginous pads on the surface of the sheaths of the main filaments connecting those with the young attenuated trichomes. Trichomes usually single, sometimes two inside a single widened sheath, attenuated, rarely with moderately long hairs, 7–12 (17) μm wide. In senescent cultures, long trichomes not or slightly constricted at crosswalls, sometimes coiled inside the thick, robust sheath, 8–17 (19) μm wide. Meristematic zones present with densely packed short cells. Cells near the bases usually distinctly shorter than wide, rarely up to isodiametric, in hairs (when present) always longer than wide, barrel-shaped when young, rarely almost without constrictions in old filaments, granulated, intensely blue-green, sometimes with several small or a few massive granules, in short trichomes very constricted, with sub-spherical cells, dividing by centripetal binary fission. Heterocytes rare in nitrogen-rich media, in nitrogen-free medium heterocytes of different shapes and sizes, intercalary and terminal, occasionally two in a row, 10–12 (19) μm in diameter. Necridic cells with colour similar to vegetative cells, but sometimes brown. Reproducing by short, 2–8 (12) celled hormogonia, tapered to one end or isopolar, rarely with a basal heterocyte.','Shalygin et al. 2018',NULL,0,0),(1444,1742,'description','Stratum subcoriaceum multilamellosum, expansum, molle, superficie olivaceo-viride vel aerugineum, intus ± lutescens vel pallescens. Trichomata 0,8-1,5 um crassa, recta vel flexuosa, subparallele aggregata vel leviter intricata, ad genicula subito et modice constricta, apice non attenuata. Vaginis angustis, achrois, mox diffluentibus chlorozincico iodurato haud coerulescentibus. Cellulis breve cylindraceis angulis rotundatis, 1-2<sup>​plo</sup> longioribus quam latioribus, contentu non granuloso, olivaceo vel pallide aeruginoso, cum chromatoplasmate valde colorato a centroplasmate claro distincte limitato. Cellula apicalis aut supernee rotundata, aut elongata et leviter conoidea.','Stockmayer &amp; Skuja in Skuja 1937',NULL,0,0),(1445,1746,'description','Strtum compactum coriaceum, fusco-violaceum Fila valde tortuosa, arct intricata. Vaginae initio arctae, papyracerae demum diffluentes et agglutinata, chorozincico iodurato non carulescentes Trichomata pallide fusco-violacea, apice nec attenuata nec curvata, ad genicula haud constricla, 1,5 ad 2,5 um crassa; articuli subquadrati, vel diamelro fere ad dplo longiores, 2 um ad 4,5 um longi; dissepimenta quaternis granulis protoplasmaticis notata; cellula apicalis rotundata; calyptra nulla (v. s.).','Gomont ex Gomont 1892',NULL,0,0),(1446,1749,'description','Stratum gelatnosum, siccitate translucens, purpureum (ex Harvey). Fila tenuissima, mollia, valde elongata, modice flexuosa. Vaginae tenuissimae, hyalinae, papyraceae, chlorozincico iodurato non caerulescentes. Trichomata violacea (ex Harvey), ad genicula haud constricta, 1,4 ad 1,8 um crassa; articuli subquadrati (v. s.).','Gomont 1892',NULL,0,0),(1447,1752,'description','Fila tenuissima, tortilia. Vaginae hyalinae, tenuissimae, papyraceae. Trichomata dilute aeruginea, 0,75 um ad 0,8 um crassa, ad genicula constricta, apice non attenuata; articuli diametro trichomatis ad quadruplo longiores, 2,3 um ad 3,2 um longi; dissepimenta pellucida; protoplasma haud granulosum; cellula apicalis rotundata; calyptra nulla (v.s.).','Gomont 1892',NULL,0,0),(1448,1756,'description','Filaments very intricate and tortuous, with a very fragile, hyaline sheath, forming dense, thin, tough layers, light blue-green in color; trichomas 0.9-1 um diam., slightly constricted at the conspicuous cross-walls; cells homogeneous or with 1-2 coarse granules usually at the cross-walls, about four times as long as the diam.; apices neither uncinate, attenuate, nor capitate.','Gardner 1932',NULL,0,0),(1449,1760,'description','Filis angustis, plerumque valde tortuosis, interdum subrectis, stratum in superficie Phormidii formantibus; vaginis primo tenuibus hyalinis, demum modice incrassatis extus rugosis cum particulis numerosis adhaerentibus, non lamellatis; trichomatibus cum cellula apicali acuta conica, non capitatis aut attenuatis, plerumque modice inter cellulas constrictis; cellulis tam longis quam latis vel paulo longioribus, plerumque cytoplasmate homogeneo, dissepimentis indistinctis, sed interdum cum granulis dense aggregatis in utraque parte dissepimentarum; calyptra nulla. Diam. fil. = 3.4-5 um ; diam. trichi. = 2.6-3 um.','Fritsch 1912',NULL,0,0),(1450,1762,'description','Filaments short, crooked, forming a more or less compact layer on the filaments of the host, prostrate, with the ends free and more or less erect, 2.5-3 um diam.; cells quadrate to 3 times as long, pale aeruginous, protoplast homogeneous; cross-wall inconspicuous<sup>​</sup>; apices straight, blunt, not capitate; sheaths very thin, inconspicuous.','Gardner 1927',NULL,0,0),(1451,1767,'description','Ph. strato membranaceo, atro-ærugine, trichomatibus flexuoso-curvatis, saepe parallelis, aete aerugineis, 1.8-2.2 um crassis ad genicula leviter constrictis, apice rectis, interdum attenuatis, subcapitatis; articulis diametro aequalibus vel ad 3-plo longioribus, interdum granulis sparsis farctis; cellula apicali calyptram rotundatam vel depresso conicam jpaebente; vaginis mucosis, chlorozincico jodurato non coerulescentibus.','Petersen 1923',NULL,0,0),(1452,447,'description','In &nbsp;nature, &nbsp;growing &nbsp;on &nbsp;the &nbsp;bark &nbsp;of &nbsp;trees, &nbsp;wood, or concrete. &nbsp;Thallus microscopic in natureand in culture. In culture primarily growing attached to the glass &nbsp;walls &nbsp;of &nbsp;the &nbsp;test &nbsp;tubes &nbsp;in &nbsp;liquid &nbsp;media, &nbsp;and &nbsp;re-leased &nbsp;as &nbsp;tufts &nbsp;which &nbsp;detach &nbsp;and &nbsp;settle &nbsp;to &nbsp;the &nbsp;bottom &nbsp;of &nbsp;the &nbsp;test &nbsp;tube &nbsp;as &nbsp;they &nbsp;grow, &nbsp;on &nbsp;agar &nbsp;growing &nbsp;radi-ally &nbsp;from &nbsp;the &nbsp;center &nbsp;via &nbsp;hormogonia &nbsp;release, &nbsp;forming &nbsp;a &nbsp;dense &nbsp;creeping &nbsp;mat. &nbsp;Colonies &nbsp;spherical &nbsp;when &nbsp;de-veloping &nbsp;from &nbsp;akinetes, &nbsp;elongate &nbsp;when &nbsp;developing &nbsp;from &nbsp;hormogonia, &nbsp;eventually &nbsp;aggregated &nbsp;loosely &nbsp;into &nbsp;macroscopic &nbsp;thalli &nbsp;through &nbsp;release &nbsp;of &nbsp;difflu-ent &nbsp;mucilage. &nbsp;Akinetes &nbsp;apoheterocytic, &nbsp;spherical &nbsp;or &nbsp;subspherical, &nbsp;granulated, &nbsp;developing &nbsp;from &nbsp;vegetative &nbsp;cells in trichomes, germinating into two equal vegeta-tive &nbsp;cells &nbsp;or &nbsp;alternatively &nbsp;into &nbsp;a &nbsp;large &nbsp;vegetative &nbsp;cell &nbsp;and a smaller heterocyte, either of which develops into &nbsp;spherical colonies with a firm mucilage layer, which eventually &nbsp;become &nbsp;larger &nbsp;colonies &nbsp;enclosed &nbsp;within &nbsp;a &nbsp;diffluent mucilage. Hormogonia developing from older more diffuse colonies; when first formed motile, short, lacking firm mucilage, later immotile with heterocytes and &nbsp;akinetes, &nbsp;developing &nbsp;into &nbsp;multiseriate &nbsp;filaments, which &nbsp;eventually &nbsp;become &nbsp;elongate &nbsp;colonies &nbsp;enclosed &nbsp;in a firm mucilage. &nbsp;Cells quadratic in young hormo-gonia, becoming spherical or subspherical as filament matures, dividing perpendicular or longitudinal to the main &nbsp;axis &nbsp;of &nbsp;filament. &nbsp;Heterocytes &nbsp;spherical, &nbsp;com-pressed subspherical or oval.','Hentsche et al. 2017',NULL,0,0),(1453,1781,'description','Fila solitaria, inter alias algas sparsa, recta vel laxe undulata. Trichomata 2 um crassa, submoniliformia; articuli paulo breviores quant latiores, ad dissepimenta evidenter constricta, contentu subtiliter granuloso; dissepi- menta pellucida; cellulla apicalis rotundata, nec capitata nec incrassata; vaginae tenues et firmae.','Frémy 1945',NULL,0,0),(1454,1789,'diagnosis','Filamenta plus minusve recta vel flexuosa, longa, rare solitaria, plerumque in strata macroscopica, dense paralleliter vel irregulariter contorta, cum vaginis tenuis, incoloris, diffluentibus. Trichomata cylindrica, pallide virides vel aeruginosae, ad dissepimenta non, rare paucim constricta, ad apices non attenuata, cum articulis paulo visibilis, 1.5–2.0 μm lata. Cellulae plus minusve isodiametricae, interdum paulo longiores quam latae, contentu homogeneo; cellulae terminales cylindricae, rotundatae, cum membrana exterior paucim incrassata. Hormogonia curta, cum cellulis paucis. - Habitatio: Strata communes in paludis alcalinis salinisque, bentice dominans et fluitantes.','Turicchia et al. 2009',NULL,0,0),(1455,1795,'description','Stratum extended, soft leathery, up to 1.5 mm. thick, easily torn, surface sometimes tomentose with dendritic lime; yellowish green to grayish within. Trichomes more or less parallel or irregularly disposed, often contorted, densely packed, cir. 0.4 um in diameter. not constricted at the easily visible cross walls, yellowish green; apices straight, not tapering. Sheaths confluent, invisible, without pigmentation. Cells 2-3 diameters in length; end cells rounded, not calyptrate.','Copeland 1936',NULL,0,0),(1456,1797,'description','L. solitaria et sparsa, trichomatibus subflexuosis, libere natantibus, distincte articulatis; vaginis arctis, achrois; articulis diametro duplo; cytioplasmate pallide aerugineo et homogeneo. Lat. fil. 1.5-1.8 um.','Wset 1892',NULL,0,0),(1457,1799,'description','Fäden gekrümmt, 1 bis 1.8 um dick, zu wenig compactem, schleimigem, lebhaft spangrünem Lager verflochten. Veget. Zellen fast so lang wie breit, an den Scheidewänden leicht eingeschnürt ; Scheiden dünn, farblos.','Hansgirg 1892',NULL,0,0),(1458,1803,'description','Slratum luteo-viride, lamellosum. Vaginae in mucum gelalinosum amorphum chlorozincico iodurato non caerulescentem protinus diffluentes. Trichomata aeruginosa, recta, ad genicula constricta, distincte articulata, apice longe attenuala arcuata vel tortuosa haud capilata, 2 um ad 2,8 um crassa; articuli diametro trichomatis ad quadruplo longiores, 6 um ad 8 um longi; protoplasma homogeneum, floccosum aut grosse granulosum; cellula apicalis plus minusve acute conica; calyptra nulla (v. s . ) .','Gomont 1892',NULL,0,0),(1459,1805,'description','Fäden 1.8 bis 2.5 um dick, einzeln oder zu Bündeln vereinigt, gerade oder leicht gekrümmt. Veget. Zellen 1/2 bis 1 1/2 mal so lang als breit, mit blau-, oder olivengrünem Inhalte. Endzeilen öfters gebogen.','Hansgirg 1892',NULL,0,0),(1460,1808,'description','Stratum laete aerugineum, tenue, membranaceum, expansum. Fila elongata, subrecta, dense intricata. Vaginae tenues, in mucum fibrosum demum diffluentes, chlorozincico iodurato caerulescentes. Trichomala laete aeruginosa, recta, ad genicula leviter constricta, plerumque indistincte arliculalta, apice initio recta deinde uncinata et attenuata baud capitala, 1 um ad 2 um crassa; articuli diametro teichomatis ad triplo longiores, 2,5 um ad 5 um longi; protoplasma homogeneum; cellula apicalis demum acute conica; calyptra nulla (v.v.).','Gomont 1892',NULL,0,0),(1461,1810,'description','Fila gracilia, elongata, flexuosa, vulgo parce pseudoramosa, pseudo-ramis saepius solitariis. Vaginae hyalinae tenuissimae, cylindraceae, chlorozincico iodurato non caerulescentes. Trichomata dilute aeruginea, non torulosa, 0,95 um ad 1,5 um crassa; articuli diametro trichomatis longiores, 2 um ad 6 um longi; dissepimenta binis granulis protoplasmaticis notata; cellula apicalis rotundata (v.v.).','Bornet &amp; Flahault ex Gomont 1892',NULL,0,0),(1462,1812,'diagnosis','Filamenta recta vel arcuata, solitaris, 1-16 um lata, cum vagina fina, sine colore, hyalina, ad trichomatibus contigua. Trichomata 0.8-1.5 um lata, palescens aeruginea, ad apices not attenuata, ad dissepimenta non constricta, saepa cum 2 granulis apud dissepimentis. Cellulae cylindricae, longior quam latae, rare isodiametricae, 1-5-7 um longae, cellulae apicalis rotundatae.','Anagnostidis 1961 as Lyngbya limnetica',NULL,0,0),(1463,1815,'diagnosis','Filamenta solitaria vel in fasciculos contorta, irrgulariter vel &nbsp;plus minusve regulariter spiraliter flexuosa (spirae 10-12 um latae, l8-24 um longae), &nbsp;plus minusve 1.8-2 um lata; vaginae tenues, sine colore; trichomata pallide aeruginea, 1.5- 2 um lata, ad dissepimenta haud, seu paulum constricta, cylindrica, ad apices haud attenuata. Cellulae &nbsp;1.2-3 um longae, contentu homogeneo, interdum cum granulis, solitariis subapicalibus. Cellulae apicales cylindricae rotundataeqe.','Anagnostidis 2001',NULL,0,0),(1464,1816,'diagnosis','Strato olivaceo, tenui, membranaceo, valde expanso; filis varie flexuosis, dense intricatis;vaginis tenuibus, mucosis, plerumque inconspicuis, in mucum amorphum omnio diffluentibus, chlorozincico jodurato non coerulescentibus; trichomatibus flavescenti-viridibus, ad genicula non constrictis aut rarius leviter constrictis, apice interdum attenuatis, 2-2.4 um crassis; articulis quadratis vel saepius longioribus, 2.5-6 um long; dissepimentis bene conspicuis, distinctissimis; contentu plerumque granuloso aut rarius homogeneo; cellula apicali acute conica; calyptra nula.','Elenkin 1949',NULL,0,0),(1465,1818,'diagnosis','','Gomont 1899',NULL,0,0),(1466,1819,'diagnosis','No spatially delimited mucilaginous structures observed in this species in contrast to all other known <em>Aphanothece </em>and <em>Gloeothece </em>species. Note: observations are based exclusively on culture material.','Mareš et al. 2019',NULL,0,0),(1467,1819,'description','Cells solitary, unable to float in liquid medium. Mucilaginous envelopes absent. Cells broadly oval to cylindrical with rounded ends, 4–9 um long, 3–5 um wide, bright to pale bluegreen, cell content homogenous or finely granular. No large granules visible in TEM. Secondary structure of the D1-D10 helix distinct from all other taxa in this study, with a short helix on the 30 side of the central helix, and a single adenosine residue on the 50 strand opposite the unilateral bulge on the 30 strand, with D1-D10, BoxB, and V3 helices all unique among the ITS regions studied in this work.','Mareš et al. 2019',NULL,0,0),(1468,1821,'description','In liquid cultures, coccoid cyanobacteria, unicellular cells without envelopes, blue-green when fresh, yellow or yellow green and larger when old, spherical, oval, irregular or elongated. Colonies microscopic or macroscopic, not floating, with irregularly and densely arranged cells in common sheath, dark green when fresh, yellow when old. Thylakoids irregularly arranged. Sheath rigid, thick, not stratified and diffluent, colorless or golden. Reproduction by binary fission in three or more planes.','Wang et al. 2019',NULL,0,0),(1469,1822,'description','Morphological analysis of <em>Sinocapsa zengkensis </em>CHAB 6571 showed that this strain presented unicellular cells that irregularly aggregated to form dense colonies (Fig. 1c, 1f) by common rigid colorless or golden envelopes (Fig. 1h) without floating (Fig. 1b), in liquid cultures. Unicellular cells exhibited spherical or irregular-round shape (average longitudinal diameter of 4.88 ± 0.64 μm, and average transverse diameter of 3.95 ± 0.39 μm, larger than that of <em>Aliterella </em>spp.) and with visible chromatoplasm (Fig. 1d arrow) suggesting the distribution of concentrated thylakoids on the periphery of cells in fresh cultures. Unicellular cells were not surrounded with mucilaginous envelopes (Fig. 1d–e). However, the occurrence of several prominent granules with the disappearance of partial thylakoids within the cells of 4–month–old cultures were obvious (Fig. 1g), which old cells had larger cell sizes (average longitudinal diameter of 5.77 ± 0.84 μm, and average transverse diameter of 4.41 ± 0.57 μm). And the color of 6–month–old cell contents turned all yellow. The ultrastructure of 2–month–old cells showed the irregular arrangement of thylakoids in the cytoplasm (Fig. 2) and the initial accumulation of cyanophycin (Fig. 2a, 2c–d, 2f Cg). Sheath of the colonies were thick (up to 4 μm or thicker) but not stratified or diffluent under light microscope (Fig. 1f) and TEM (Fig. 2f). The ultrastructure also indicated that the cellular morphology of CHAB 6571 was the consequence of the increase in number and volume of cells nested in a shared common envelope, which the traces of squeezed envelope were visible between cells (Fig. 1h, Fig. 2d–e). Division of cells was in three or more planes by binary fission and no baeocytes were observed during the entire cultivation process.','Wang et al. 2019',NULL,0,0),(1470,1822,'etymology','zengkensis refers to the Village Zengkeng','Wang et al. 2019',NULL,0,0),(1471,1818,'other','Stratum olivaceum, expansum, lamellosum, stratis pluribus superpositis, papyraceis compositum. Fila muco tenaci, chlorozincico iodurato caerulescenti, agglutinata, parallela, tenuissima, recta, rigida. Vaginae tenuissimae, hyalinae. Trichomata dilute aeruginea, apice recta, haud attenuata, ad genicula non constricta, 0,6-0,8 &nbsp;um crassa, longissime articulala; articuli ad undecies diametro longiores; cellula apicalis rotundata; calyptra nulla.','Gomont 1899',NULL,0,0),(1472,1826,'diagnosis','Stratum lubricum, &nbsp;expansum, &nbsp;lamellosum, &nbsp;fere ad tria &nbsp;centimetra &nbsp;crassum, &nbsp;lamellis &nbsp;discoloribus, &nbsp;superioribus &nbsp;sordide &nbsp;viridibus, &nbsp;inferioribus &nbsp;decoloratis, &nbsp;compositum. &nbsp;Fila flexuosa, dense intricata. &nbsp;Vaginae &nbsp;arctae, &nbsp;papyraceae, demum &nbsp;in &nbsp;mucum &nbsp;tenacem &nbsp;diffluentes &nbsp;et agglutinatae, &nbsp;chlorozincico iodurato caerulescentes. Trichomata &nbsp;aeruginea; apice recta, non atltenuata, ad genicula haud constricta, 2um ad 2,5 um crassa; articuli diametro longiores, 3,3 ad 6,7 um longi; dissepimenta binis vel quaternis granulis proloplasmaticis notata; cellula apicalis rotundata; calyptra nulla.','Gomont 1892',NULL,0,0),(1473,1830,'description','Stratum gelatinous, homogeneous, translucent and pale blue-green to golden-green, up to 1 cm thick, frequently and characterlstically with long or short, flexible, gelatlnous. erect or waving cords &nbsp;arising &nbsp;from the upper surface, 3-10 mm in diameter and up to 0.6 m. long, bearing at their upper ends gasfllled sacs or vesicles 1-6 cm in dlameter, that tend to float at the surface and support the cords in an erect position. Trichomes not crowded, straight to flexuous, not contorted, &nbsp;often more or less parallel, alike in all parts of the plant &nbsp;mass, 2.6-3.2 um In dlameter (usually 3.0 um), often very slightly constricted at the cross walls. Sheaths invisible, completely confluent into a colorless, homogeneous matrix. Cells cylindrical, 6-15 um in length (usually 8-12 um), much longer than their diameter, &nbsp;frequently spaced in the trichome with the gap between &nbsp;cells up to 0.5 um, pale blue-green, wlth usually two polar granules which lie at or near &nbsp;the end walls. &nbsp;Apices straight, not tapering (except for the end-cells). End-cells at first rounded, then obtusely pointed, gradually becoming long, sharp-pointed, and sometimes with a tiny bent hook on the tip, without calyptra; termlnal half or two-thirds of each end cell modifled, remainder of cell &nbsp;normal.&nbsp;','Copeland 1936',NULL,0,0),(1474,1833,'description','Stratum aeruginous; filaments often strongly bent; sheath not visible; trichomes pale aeruginous, not constricted at joints, with apex sharply bent, briefly attenuate and not capitate, 2.5-3 um in diameter, the dissepiments generally distinct; articulation 1.5-2.5 times as long as the diameter; protoplasm commonly containing granules; dissepiments sometimes marked by granuules; apical cell acutely conical; no calyptra.&nbsp;','Tilden 1898',NULL,0,0),(1475,1835,'description','Stratum aerugineum aut nigrescens, mucosum vel membranaceum; trichomatibus rectis undulatisve, fragilibus, paralleliter in muco amorpho hyalino chlorozincico iodurato haud caerulescente dispositis, ad genicula evidenter constrictis numquam torulosis, 1.0 um ad 2.5 um crassis, superne rectis vel curvatis uncinatisve, ad apices sensim et longe attenuatis et acutis; articulis subquadratis aut diametro usque duplo longioribus, 1.5 um ad 5 um longis; protoplasmate per totam cellulam homogeneo, raro tenui-granuloso; dissepimentis conspicuis, haud granulatis; cellula apicali acute conica, haud capitata, sine calyptra.','Drouet 1939',NULL,0,0),(1476,1839,'description','Strato tenui membranaceo, plerumque e filis brevibus, series laxas haud regulariter dispositas formantibus. Trichomatibus as genicula non constrictis, 0.6-0.8 um lat., dissepimentis tenuibus, sed semper bene conspicuis. Vaginis diffluentibus, chlorozincici iodurato non coerulescentibus. Articulis 3.4-5 um long, id est diametro ad sextuplo longioribus, protoplasmate homogeneo. Cellulis apicalibus rotundatis.','Anissimova in Elenkin 1949',NULL,0,0),(1477,1848,'description','Trichomatibus crassioribus, distincte articulatis, laxe spiralibus, agilibus saepe invicem complexis, 10 um crassis; articulis diam. 2-pIo brevioribus; anfractuum distantia 9,5 um; apiculo leviter attenuato, obtuso; contentu olivaceo, homogeneo, pellucido.','Forti 1907',NULL,0,0),(1478,1852,'description','Strato aerugineo, gelatinoso;trichomatibus cire, 9 um crassis, articulatis, laxe spiraliter tortis, rigidulis, fragilibus, articulis levinus homogeneis diam. subaequatilis.','Forti 1907',NULL,0,0),(1479,1856,'description','Thallus braun, aus festsitzenden Fäden, rasenbildend auf Stamm und Ästen einer entrindeten Fichte in der Spritzzone eines kleinen Wasserfalles. Liegende Fäden sohlenartig ein dichtes Geflecht bildend, Fadenenden senkrecht vom Substrat abstehend. Fäden bis 2 mm lang, dünn, 2—3,5 um breit (in fixiertem Zustande bis 5 um &nbsp;breit) äusserst spärlich scheinverzweigt mit dicken, festen, farblosen, geschichteten Scheiden, &nbsp;hormogonienbildend. Die einzelnen Schichten der Scheide an ihrem Ende glockenförmig erweitert, sonst auf ihrer ganzen Länge (kaum sichtbar) parallel geschichtet, langsam aufquellend. Zellen in älteren Trichomteilen 1,7—2,5 um (meist 2,0 um) breit, meist länger als breit, quadratisch oder in den Teilungszonen kürzer als breit, an den Querwänden allermeist nicht eingeschnürt, an den Fadenenden meist leicht eingeschnürt bis tonnenförmig. Zellen mit wenig Ectoplasten, zuweilen an den Querwänden unregelmässig granuliert. Enden der Trichome mit nicht teilungsfähiger kopfiger Endzelle; diese ist teilweise bis vollständig vakuolisiert. Von den übrigen Arten der Gattung verschieden durch die kopfige Endzelle, die subterminale Teilungszone und die seltenen Verzweigungen.','Jaag 1935',NULL,0,0),(1480,1866,'description','Stratum tenere pelliculosum, griseo-coeruleo-viride, siccitate griseo-luteolum, ad saxa irrigata sub cataractis expansum; fila elongata, intricata, apice 3.5-3.5 um crassa, in parte media 3-3.5 um crassa; vaginae hyalinae, firmae, mediocriter crassae, non lamelosae vel aetate provecta indistinctae lamellosae, apice difluentes at incrassatae, chlorozincico jodurato coerulescentes; trichomata pallide aeruginea in apice incrassata, 2.5-3.5 um crassa, in media parte 1.6-2.4 um crassa; cellula apicalis late globosa cum vacuolis magnis; cellulae subapicales ad dissepimenta evidenter constricta, cellulae in media parte filorum cylindricae, subquadratae, ad dissepimenta granulatae. Propagatio hormogoniis et filorum fragmentatione.','Starmach 1958',NULL,0,0),(1481,1593,'description','Caspites molles, sordide virescentes aut obscure aeruginei, ad tria centimeta alti. Fila subdicholome aut fasciculatoramosa. Vaginae hyalina vel sordide luteo-virescentes, &nbsp;crassae, agglutinantes, transverse repetite corrugatrae et quasi squamosae, non diffluentes, apice clausae et acuminatae aut aperlae. Trichomata aeruginosa, intra vaginam ad basim filorum pauca, superne permulta, subrecta, parallela, haud funiformi-contorta, ad genicula constricta, 4 um ad 5.5 um crassa articuli subquadrati vel diametro trichomatis ad triplo longiores, 3.5 um ad 12 um longi, interdum protoplasmate grosse granuloso farcti; dissepimenta haud granulata; cellula apicalis acute conica.','Kützing ex Gomont 1892',NULL,0,0),(1482,1868,'description','Caespites penicillati, molles, fluctuantes, nunc obscure, nunc laete virides. Fila pseudo-ramosa, pseudo-ramis adpressis. Vaginae hyalinae, mucosae, subcrassoe, superficie leves aut rugosae et corrugatae, apice clausae et acuminatae vel apertae. Trichomata pallide aeruginosa, aut violascentia, parallela, subrecta aut funiformi-contorta, apice acuminata, &nbsp;ad genicula non constricta, 7 um ad 10 um crassa; articuli diametro trichomatis duplo ad quadruplo breviores, 2 um ad 4 um longi; dissepimenta frequenter granulata; cellula apicalis obtuse conica (v. s.).','Gomont 1892',NULL,0,0),(1483,1869,'description','Cespite parvulo, vix semiunciali, virldi; vaginis a basi 1/60 lin. crassa ad 1/250 lin. attenuatis, achromaticis; filis initio pulchre aerugineis, apice obtusis, obsolete articulatis, articulis diametro aequalibus, 1/750 lin. crassis, deinde pallldioribus et dlvlsione longitudinali et transversali in gonidia 1/1500 lin. crassa, seriata, diametro 2-4plo longiora, collapsls. (Slrocoleo Gujanensi affine, sed multo tenuius. Genus accuratius observandum).','Zeller 1873',NULL,0,0),(1484,1872,'description','Cespite parvulo, vix semiunciali, viridi; vaginis a basi 1/60 lin. crassa &nbsp;ad 1/250 lin. attenuatis, achromaticis; filis initio pulchre aerugineis, apice obtusis, obsolete articulatis, articulis diametro aequalibus, 1/750 lin. crassis, deinde pallidioribus et divisione longitudinali et transversali in gonidia 1/1500 lin. crassa, seriata, diametro 2-4plo longlora, coUapsls. (<em>Slrocoleo Gujanens</em>i affine, sed multo tenuius. Genus accuratius observandum).&nbsp;','Zeller 1873',NULL,0,0),(1485,1875,'description','Thallus gelatinous, mucilaginous, microscopic, attached to the substrate. Trichomes loosely entangled, motility present: oscillation and rotation, isopolar, cylindrical, not constricted or slightly constricted at the cross walls, bent at the tip, gradually attenuated toward the apex. Cells isodiametric or shorter or longer than wide. Cell content homogeneous or finely granular. Apical cell conical rounded and narrowed calyptra absent. &nbsp;Reproduction by disintegration of trichomes into hormogonia by necridic cells.','Buch et al. 2017',NULL,0,0),(1486,1875,'etymology','koinos (Gr. adj.) = common, ordinary (referring to the morphology of trichome); nema (Gr. n.) = thread; Koinonema = ordinary filament','Buch et al. 2017',NULL,0,0),(1487,1876,'description','Thallus gelatinous, mucilaginous, microscopic, attached to the substrate. Trichomes loosely entangled, motility present: oscillation and rotation, isopolar, cylindrical, not constricted or slightly constricted at the cross walls, gradually attenuated and bent toward the apex, 3–6.4 um wide. Cells 0.6–1.8 time longer than wide, 3–9 um long. Cell content blue-green, homogeneous, or finely granular. Apical cell conical rounded and narrowed, calyptra absent, 2–4.4 um wide, 3–8.5 um long.','Buch et al. 2017',NULL,0,0),(1488,1877,'description','Cespitose short mats brown to blackish (Figs. 1, 2), filaments cylindrical (Fig. 13), straight or curved; parallely oriented or intermingled, sometimes forming fascicles 200–300 μm long and 5–12 μm in diameter, without a common sheath (Figs. 2, 3, 20, 21). Falsely branched, branches tightly joined or irregularly divaricated to the main filament (Figs. 4, 8, 11, 21, 24). Trichomes 3–6 μm wide (Figs. 3, 5), constricted at cross-walls (Figs. 15, 16). Cells cylindrical to barrel-shaped (Figs. 15, 16), shorter than wide, 3–6 μm wide, 1–3 μm long, with slightly granulated content. Terminal cells widely rounded, sometimes nearly spherical, hyaline to greenish or yellowish (Figs. 12, 15, 16) (2-4 μm long × 3–6 μm wide). Sheaths firm, stratified, slender, hyaline (Fig. 16) to thick and amber or dark yellowishbrown, often widening with pronounced, rounded terminals (3–7 μm in diameter) (Figs. 11, 12, 16), generally closed and rarely opened at the apex (Figs. 10, 14). Heterocytes spherical, ovoid to cylindrical (Figs. 4, 5, 9, 11), 4–6 μm in diameter, 4–8 μm long (Fig. 5), one basal (Figs. 4, 8, 11, 19), rarely two (Fig. 9), and less frequently intercalary. Akinetes not detected. Reproduction by hormogonia (Figs. 6, 7, 18, 22, 23).','González-Resendiz et al. 2013',NULL,0,0),(1489,1879,'description','L. terrestris, strato spongioso membranaceo aureo-fulvo vel flavo; filis dense intricatis, flexuosis vaginis firmis, glabris et lamellosis, flavis vel flavo-brunneis trichomatibus aerugineis, ad dissepimenta leviter constrictis, apicibus haud attenuatis; cellulis quadratis, nonnunquam diametro paullo brevioribus; protoplasmate delicate granulato. Crass. fil. 13.5-14.5 um; crass. trich. 8.5-9.5 um.','West W. et G.S.&nbsp; 1897',NULL,0,0),(1490,1883,'description','Thallus macroscopic, green; filaments long, straight, curved, sometimes loose and solitary, frequently presenting untangled arrangements forming long rope-like structures; occasionally with false branching in mature filaments. Sheaths thin, colorless, distant from the trichomes, closed at the ends, opened after hormogonia release. Trichomes sometimes with exceeding sheath, distinctly constricted at the cross walls; cells usually rectangular, barrelshape, isodiametric or longer than wide, 1.3–1.7 μm long, 0.7–1.5 μm wide; apical cells usually rounded to slightly conical, without calyptra; thylakoids arranged peripherally; reproduction by hormogonia by help of necridic cells.','Soares et al. 2019',NULL,0,0),(1491,1567,'description','Stratum expansum, tomentosum, fusco-purpureum. Fila varie curvata &nbsp;et &nbsp;dense intricata. Vaginae purpurae, saepe apice hyalinae, &nbsp;nonnunquam stratis discoloribus, &nbsp;internis coloratis, externis hyalinis, formatae, firmae, demum cras­sissimae et valde lamellosae, apice acuminata et fibrillosae, chlorozincico iodurato caerulescentes. Trichomata &nbsp;aerugi­nosa, vulgo ad &nbsp;genicula constricta, 8 ad 19 um crassa; articuli diametro trichomatis subaquilongi vel eo ad triplo breviores, 4·.5 &nbsp;ad 12 um longi, protoplasmate granuloso farcti; &nbsp;cellula apicalis attenuato-obtusa.','Kützing ex Gomont 1892',NULL,0,0),(1492,1885,'description','Stratum olivaceo-violaceum vel rubrum; fila elongata, 10— 14 um crassa, recta; vaginae tenues, hyalinae, aetate provecta saepe rubescentes, chlorozincico iodurato non caerulescentes. Trichomata aeruginea vel violascentia, ad genicula haud constricta, apice non attenuata, 8—12 um, crassa; articuli diametro trichomatis aequates vel duplo-triplo breviores; dissepimenta non granulata; cellula apicalis rotundata, calyptra nulla.','Wille 1914',NULL,0,0),(1493,1887,'description','Stratum natans, expansum, aerugineo-sericeum. Fila recta plus minusve intricata. Vaginae hyalinae, firmae, &nbsp;tenues, lamellosœ, aetate erosae et fibrosae, chlorozincio iodurato non cœrulescentes, Trichomata luteole-viridia, ad genicula non constricta, apice haud attenuata, 9 ad 10 um crassa, articuli 3,5 ad 4 um longi ; protoplasma omnino homogeneum; dissepimenta inconspicua, granulorum delicatissimorum lineis binis obducta; cellulla apicalis rotundata, calyptra nulla.','Frémy 1923',NULL,0,0),(1494,1891,'description','Thallus blue-green. Filaments long, straight to slightly curved, trichome unbranched. Sheath absent. Cells much longer than wide, cylindrical, apical cells with flat ends, constrictions at the cross walls distinct.','Chakraborty et al. 2019',NULL,0,0),(1495,1892,'description','Filaments typically unbranched, straight, isopolar cyanobacterium attached to the soil surface (mainly subaerophytic) growing as an extensive mat-like biofilm. Cell shape appears to be having a slight broad apex and narrow base, much longer than wide, 1.25–2.6 μm long, 0.4–0.6 μm width, mucilaginous sheath completely absent, cell contents homogeneous, green without any granulated appearance, aerotopes absent, terminal cells consist of typical flattened ends. No heterocytes and akinetes. Cell division takes place by asymmetrical binary fission. Reproduction via the formation of hormogonia with the help of straight fragmentation of trichomes without producing any necridic cells.','Chakraborty et al. 2019',NULL,0,0),(1496,1891,'other','Thallus light greenish in color. Filaments long, straight, unbranched. Trichome covered with a thin diffluent mucilaginous sheath, cells much longer than wide, distinct constrictions at the cross wall.','Chakraborty et al. 2019',NULL,0,1),(1497,1893,'description','Thallus light greenish in color. Filaments long, straight, unbranched. Trichome covered with a thin diffluent mucilaginous sheath, cells much longer than wide, distinct constrictions at the cross wall.','Chakraborty et al. 2019',NULL,0,0),(1498,1894,'description','Filaments typically unbranched, straight, isopolar cyanobacterium attached to the soil surface (mainly sub-aerophytic) growing as an extensive mat-like biofilm. Cell shape cylindrical, appears to be elongated, much longer than wide, 1.8–3.5 μm long, 0.8–1.8 μm width, facultative, mucilaginous sheath facultatively present, cell contents homogeneous, green without any granulated appearance, aerotopes absent, terminal cells consist of typical flattened ends. No heterocytes and akinetes. Cell division takes place by asymmetrical binary fission. Reproduction via the formation of hormogonia with the help of straight fragmentation of trichomes without producing any necridic cells.','Chakraborty et al. 2019',NULL,0,0),(1499,1895,'diagnosis','Stratum tenue, nigro-fuscum. Fila varie curvata et dense intricata. Vagiae firmae, modice crassae, hyalinae vel sapius brunneo-purpurea (in speciminibus siccis), apice haud raro contractae, chlorozincico iodurato &nbsp;caerulescentes. Trichomata aeruginosa, ad genicula haud constricta, extra vaginam saepius curvata, 4 ad 6,6 um crassa; articuli diametro trichomatis quam saepissime longiores , 4,4 ad 9 um longi, protoplasmate obscure granuloso farcti. Cellula apicalis rotundata aut subconica (v. s.).&nbsp;','Gomont ex Frémy 1937',NULL,0,0),(1500,1899,'diagnosis','Strato expanso, obscure purpureo; filamentis curvatis, densissime intricatis; vaginis firmis, crassis, obscure caeruleis vel purpureas, laevibus, chitinosis; trichomatibus tenuibus, ad genicula non-constrictis, 3-4 um crassis; articulis quadratis, diametro brevioribus, protoplasmate grosse granuloso; dissepimentis haud granulosis, saepe obliquis vel curvatis; apicibus rotundatis, non-capitatis; calyptra nulla.&nbsp;','Ghose 1924',NULL,0,0),(1501,1900,'description','Filaments forming a felt–like thallus, erect, more or less parallel, tortuous 23–33 μm diam., sometimes slightly tapered from the base towards the ends, intensely branched. Branches identical to the main filament, bending toward the apex. Sheaths massive, hyaline, yellowish, mosaic–like sculptured with irregular margins. Trichomes with uni– and multiseriate parts 16–25 μm diam, composed by dark–green compressed or spherical cells, 5–11 μm diameter. Apex rounded, usually uniseriate, slightly tapered or not. Heterocytes lateral, irregulary sphaerical.','Hentschke et al. 2019',NULL,0,0),(1502,1901,'description','(Culture conditions) Mat creeping on agar, pale blue-green to olive-green in colour. Filaments long, immotile, solitary, occasionally forming spirals under normal light conditions of 27 μmol m-2 s-1 (Fig 1A and 1C). Under low light intensity of &lt;4 μmol m-2 s-1, uniseriate trichomes can lie parallel or twisted around one another within a common sheath (Fig 1D and 1E). This resembles nodule formation whereby filament width in these areas<br>becomes wider, up to 5.0 μm wide (Fig 2C–2E). Cells 1.0 (1.5)– 2.0 μm wide, 1.0–2.0 (2.3) μm long, shorter to longer than wide, discoid to barrel-shaped (Fig 2A–2G). Apical cells rounded, non–capitate, without calyptra and lacking granules (Fig 2G). Sheath colourless, thin.','Radzi et al. 2019',NULL,0,0),(1503,1902,'description','Cells approximately isodiametric, 4.5–6.0(7.0) μm wide, 3.5–5.5(7.0) μm long, barrel shaped, distinctly constricted at the cross walls, with granulated, yellow-brown content without aerotopes. Apical cells rounded, without calyptra, of the same dimensions as other cells in the filament (Figs 4B, E, G). Sheath wide, distinctly lamellate, yellow to brown, widely open at the tip, considerably longer than the trichome (Figs 4B, E–G). Filament, including the sheath, (25)30–40(50) μm wide. Generally one trichome per sheath, two in rare cases of pseudobranching (Fig. 4F). Reproduction by disintegration of the ends of trichomes into one or more motile hormogonia (Fig. 4C) with 8–22 cells. Necridic cells were not observed.','Kaštovský et al. 2016',NULL,0,0),(1504,1902,'etymology','From the Latin adjective latissimus (widest), referring to the extraordinary width of the filament of the species.','Kaštovský et al. 2016',NULL,0,0),(1505,1902,'eco_distro','This taxon occurred frequently on wet sandstone rocks, on top of Churí-tepui and Roraima, Venezuela. This species was observed in 10 % of the samples from Churí-tepui wet walls and previously also more frequently on Roraima (30 % of wet walls samples, identified as P. cf. notarisii, Kaštovský et al. 2011).','Kaštovský et al. 2016',NULL,0,0),(1506,1906,'description','Stratum subgelatinosum, coriaceum, Iuleo-fuscum vel olivascens, siccitate saepe nigro-violaceum. Fila tortilia, flexilia, arcte intricata. Vaginae hyalinae, leves, chlorozincico iodurato caerulescentes, initio tenues, aetate provecta ad 3 um crassae et lamellosae. Trichomata olivacea, ad genicula non constricta, apice haud attenuata, 2,5 ad 6 um crassa; articuli quadrati, aut diametro ad triplo breviores, 1,5 ad 5,5 um longi, protoplasmate granuloso, dissepimenta vulgo obducente, farcti; cellula apicalis calyptram rotundatam praebens.','Gomont 1892',NULL,0,0),(1507,1907,'description','Caespites aeruginei, siccitate saepe violascentes. Fila elongala, subflexuosa, flexilia. Vaginae hyalinae, aetate provecta crassae et rugosae, chlorozincico iodurato non caerulescentes. Trichomata pallide aeruginea, ad &nbsp;genicula haud constricta, apice non attenuata, 6 um ad 10 um crassa; articuli diametro trichomatis duplo ad quadruplo breviores, 1,75 um ad 3,3 um longi; dissepimenla inconspicua aut granulis proloplasmaticis notata; cellula apicalis rotundata; calyptra nulla.','Meneghini ex Gomont 1892',NULL,0,0),(1508,1908,'description','Stratum tenuissimum, mucosum, fusco-rubescens, Algas majores, saxa limumque velamine continuo obducens. Trichomata siccitate viridescentia, valde elongata et flexilia, agglutinata, in spiram laxissimam, diametro 4 um aequantem contorta, ad genicula haud constricta, apice plus minusve longe attenuata et subcapitata, 2 um ad 3 um crassa; anfractus 11 um ad 13 um inter se distantes; articuli subquadrati aut diametro ad triplo longiores, 3,5 um ad 7 um longi; dissepimenta fere inconspicua, haud granulata.','Gomont 1892',NULL,0,0),(1509,1909,'description','Filaments closely intertwined, forming a loose floccose stratum, of moderate length, 30-36 um diam.; trichomes not constricted, neither attenuated nor capitate, 16-20 um diam.; cells one-third to one-half as long as the diameter, homogeneous, bright aeruginous, cross-walls very distinct; apical cell rounded, wall not thickened · sheath rigid, at first hyaline homogeneous later changing to pale rose-pink and becoming decidedly lamellose, <br>the ends usually extending much beyond the trichomes, and becoming collapsed and more or less lacerated.','Gardner 1927',NULL,0,0),(1510,1913,'description','L. filis sparsis inter stratum algarum Myxophycearum, subrectis; vaginis firmis achrois distincte lamellosis; trichomatibus Iaete aerugineo-coeruleis, inter cellulas non constrictis, massa intercellulari inflato- torulosa et refringenti erebro interruptis, apicibus rectis; cellulis diametro trichomatis quadruple brevioribus, cytioplasmate minute granulate; cellula apicali elongato-conica et pallidissime aeruginea. Crass.fil. 12-12.5 um, trich. 8.5-9.5 um; long. cell. 2-2.4 um.','West et West 1911',NULL,0,0),(1511,1916,'description','L. lacustris, aeruginosa, mucoso-compacta; trichomatibus pulcherrime aeruginosis (diam. 1/300´´´ s.v.), &nbsp;flexuosis, intricatis , rigidulis, distinctissime articulalis; articulis vel duplo brevioribus, &nbsp;dimidiatis, vel 3-4 plo brevioribus, non dimidiatis, granulosis.','Kützing 1843',NULL,0,0),(1512,1917,'description','Stratum aerugineum vel fusco-viride, crustosum, late expansum, filis longis, inferne tortuosis et compacte intertextis, superne in fascicules breves coalitis; vaginis primum hyalinis demum pallide roseis et fusco-rubris, tenuibus, inconspicue lamellosis, chlorozincico iodurato caerulescentibus; trichomatibus aerugineis, 3 um ad 5 um crassis, ad genicula paullo constrictis, ad apices leviter attenuatis; articulis diametro usque ad duplo longioribus, dissepimentis pellucidis non granulatis, protoplasmate aerugineo tenui-granuloso; cellula apicali conica, membrana superna non incrassata.','Drouet 1942',NULL,0,0),(1513,1917,'etymology','This species is named in honor of Dr. Gregorio T. Velasquez of the University of the Philippines.','DRouet 1943',NULL,0,0),(1514,1919,'description','Stratum initio adhaerens, deinde libere natans, lubricum, submolle, extus ferrugineum, intus sordide olivaceo-viride. Fila elongata, tortuosa, arcte intricata. Vaginae hyalinae, interdum luteolae, !eviter mucosae et agglutinantes, ad 2 um crassae, chlorozincico iodurato caerulescentes. Trichomata aeruginea, ad genicula non constricta, apice nec attenuata nec capitata, 2,8 um ad 3,2 um crassa; articuli vulgo subquadrati, rarius diametro breviores aut eo ad duplo longiores, 2 um ad 6,4 um longi; dissepimenta pellucida, nonunquam granulata; cellula apicalis rotundata; calyptra nulla.','Gomont 1892',NULL,0,0),(1515,827,'description','Plants not forming a distinct stratum, but interspersed among other algae; trichomes relatively long and flexuous, neither constricted nor attenuated, 3.4-3.8 um diam.; cells for the most part quadrate, conspicuous by the presence of granules at the distinct cross-walls; apical cells blunt, end wall slightly thickened.','Gardner 1927',NULL,0,0),(1516,831,'description','A typo latitudine majore cellulis et apicis constante diametro differt. Cellulae longitudo : 4-6 um; latitudo : 2,5-5 um.&nbsp;','Couté 1980',NULL,0,0),(1517,1538,'description','Filaments 4-6 mm long, variable in diameter, forming a flocculent stratum, composed of 1-6 trichomes, branching fairly abundant; trichomes smooth or in part slightly constricted at the cross-walls towards the apices, 5.8-6.2 um diam.; cells quadrate to one third as long as the diameter, pale aeruginous, homogeneous; apical cell blunt, rounded, with slightly thickened terminal wall; sheaths firm, smooth, hyaline, homogeneous, 1-2 um thick.','Gardner 1927',NULL,0,0),(1518,743,'diagnosis','Trichoma libere natantia, solitaria, sine vaginis, recta vel paucim arcuata, ad dissepimenta not vel paucim constricta, plus minusve cylindrica et ad apices usu gradatim attenuata, ad 6-6.8 μm lata in media parte, apice ad 3.5-4 μm lata. Cellulae plus minusve isodiametricae vel paucim abbreviatae, contentu pallide aeruginoso vel olivaceo-viridi, interdum cum aerotopis numerosis parvis facultativis; cellula apicalis conicerotundata vel rotundata, sine calyptra. Heterocytae akinetesque carentes.','Komárek et Komárková-Legnerová 2007',NULL,0,0),(1519,895,'description','Trichomata solitaria, luteo-viridia, valde elongata, ad genicula non constricta, 8—9 um crassa, apicem versus attenuata et eximie flexuosa; articulis diametro trichomatis duplo brevioribus. apicalibus subquadratis, protoplasmate valde granuloso cum pseudovacuolis; cellula apicalis obtusa; calyptra nulla.','Woloszynska 1912',NULL,0,0),(1520,1926,'description','Filaments moderately elongated, relatively narrow and smooth, unbranched, closed at the apices, 30-50 um diam., enclosing 1-7 trichomes in any cross diameter, but many more throughout their entire length; sheath hyaline, homogeneous, moderately firm; trichomes pale aeruginous, 6.3-6.5 um diam., scattered or entwined about each other within the sheath, attenuated at the apices, straight, not capitate; apical cell blunt-conical, in part with a very slightly thickened end wall; cells short, 1.8-2.2 um long, with homogeneous contents.','Gardner 1932',NULL,0,0),(1521,1928,'description','Caespituli atro-violacei. Fila subsimplicia, rigida, recta, siccitate fragilia, fasciculato-agglutinata. Vaginae &nbsp;lyngbyaceae, papyraceae, inferne subamplae et lamellosae, superne arctae, transverse leviter corrugatae, apice contractae. Trichomata &nbsp;purpureo-chalybea vel fuscescentia, iultra vaginam plerumque solitaria et recta, aut rarius plura, arcte congesta et contorto-implicata, ad genicula non constricla, 8 um ad 10 um crassa; articuli diametro trichomatis duplo ad quadruplo breviores, 2,4 um ad 5 um longi; dissepimenta saepius granulata ;<br>apex trichomatis eximie attenuato-capitatus; cellula apicalis depresso-conica.','Kützing ex Gomont 1892',NULL,0,0),(1522,1930,'description','Trichomatibus inclusis 2-10, aequalibus, 15 um crassis, articulis obsoletis diametro 3 - 5plo brevioribus, vaginis usque 55-75 um crassis, saepius longitudinaliter striolatis .','Nägeli ex Kützing 1849',NULL,0,0),(1523,1933,'description','Strato caespitoso, deformato, erecto, sordide viridi, 6-9 cm. alto; trichomatibus inclusis in vagina communi, fasciculatis, flexuosis, intricatis; articulis irregularibus; vagina hyalina, subtilissime longitudinaliter striata, 10-12 um crassa.','Fiorini-Mazzanti ex Forti 1907',NULL,0,0),(1524,1934,'description','Filamentis longis 15-100 um latis, trichomatibus 1-7 intra vaginam gelideam dichroam extus luteam intus hyalinam aliquando transverse zonis luteofuscis provisam consociatis; cellulis 6-7 um latis, 2-4 um longis ad septum non constrictis atque cellula apicale 6-12 um longa.&nbsp;','González Guerrero 1946',NULL,0,0),(1525,1935,'description','Pulvinuli parasitici, caespitosi, globosi, rubro-sanguinei, siccitate violacei. Fila recta, e centro radiantia, parallela, fasciculato-erecta, vage pseudo-ramosa, dense aggregata. Vaginae amplae, cylindraceae, apice acuminatae aut apertae. Trichomata coccinea, recta, intra vaginam pauca vel solitaria, remota, parallela, ad genicula non constricta 5,5 &nbsp;ad 9,5 um crassa; articuli diametro irichoma tis vix aequilongi aut eo ad triplo breviores, 2,5 ad 6 um longi; dissepimenta haud granulata; apex trichomatis sublonge attenuatus, obtusus, eximie capitatus.','Gomont 1892',NULL,0,0),(1526,1937,'description','Filaments associated more or less into loose rope-like colonies interwoven among the utricles of the host; sheath very delicate and hyaline, containing few to many trichomes; trichomes cylindrical or at times slightly tapering at the apices, pale blue-green, 2.75-3.25 um diam.; cells not constricted at the dissepiments, 0.5-1.5 times as long as the diameter, the terminal cells somewhat enlarged and rounded with decidedlythickened end walls.','Setchell &amp; Gardner 1924',NULL,0,0),(1527,1939,'description','Plants either attached or free-floating in more or less flocculent masses; filaments flexuous, up to 2 cm long, with few, mostly 1 but up to 4, trichomes in a sheath; filaments with single trichome, 44-48 um diam.; sheath subgelatinous, hyaline, homogeneous, often with transverse constrictions; triehome 24-28 um diam., neither attenuate nor capitate; cells 2-3 um long, not constrieted at the cros-walls; terminal cell slightly round; end wall not at all or only slightly thickened, contents finely granular, dark blue-green.','Gardner 1927',NULL,0,0),(1528,1941,'description','Pulvinuli haemispherici, viridi-violascentes, caespitosi, mucosi, ad sesquicentimetrum alti. Fila erecta, inferne tortuosa et saepe spiraliter implicato-contorta, superne libera, subrecta, vix ramosa. Vaginae amplae, lyngbyaceae, ambitu regulares, lubricae, parum mucosae, interdum lamellosae et fibrillosae, apice plerumque apertae. Trichomata aruginosa, intra vaginam pauca, in parte superiore filorum solilaria, ad genicula constricta (in speciminibus siccis), 14 um ad 21 um crassa; articuli diameteo trichomatis triplo ad septuplo breviores, 3 um ad 5 um longi; dissepimenta granulata; apex trichomatis attenuato-truncatus.','Gomont 1892',NULL,0,0),(1529,1943,'description','Filaments erect, forming a blue-green, compact, spongy stratum of indefinite expansion on rocks; sheath &nbsp;gelatinous, moderately ample, irregular on the surface, hyaline, homogeneous, distinct at first or later diffluent; trichomes 1-8 in a sheath, separate or loosely entwined, very slightly constricted at the dissepiments, 4-4.5 um diam., straight and not attenuated at the apices; cells 2-4 times shorter than the diameter, protoplast homogeneous; apical cell moderately rounded, end wall slightly thickened.&nbsp;','Setchell et Gardner 1918',NULL,0,0),(1530,459,'description','Filaments forming expanded blue-green mats on the substratum and large floating membranaceous aggregates in older liquid cultures. Under natural conditions, thalli live solitarily or mixed with other cyanobacteria and diatoms. Slow gliding motility on solid medium. Flexuous, indefinite length long, isopolar, unbranched trichomes. Each trichome individually surrounded by a thin colorless sheath. Inside the trichomes, cells 1–3.6-fold longer than wide. Cells usually 1.2–6.5 um long and 0.8–2 um wide. Parietal thylakoids. Reproduction by trichome fragmentation into short hormogonia without necridia. Allophycocyanin and C-phycocyanin rich. Typical from thermal environments.','Sciuto &amp; Moro 2016',NULL,0,0),(1531,1944,'description','occur as mats in the nature with dark bluish green colour and mucilaginous texture; dark blue green filaments in the laboratory grown culture, which on long time incubation may start to appear yellowish in the microscope; prominently false branched with the frequency of false branching increasing with the age of culture; false branching appears both solitary and binary; branches are less in width as compared to the main filament; tapering towards the terminal cells seen prominently in all branches; sheath is prominent, thick and colourless<br>but perfectly distinct in both texture and colour; sheath present throughout the length of trichome with constrictions at the cross walls; constrictions between cells prominent in younger filaments, while the constrictions become less evident in older filaments; hormogonia present and may serve as reproductive<br>propagules; younger vegetative cells appear dark bluish green in colour, while the older ones become a bit yellowish; textured cytoplasm prominent; vegetative cells vary a lot in shape ranging from cylindrical to barrel shaped; width is usually more than the length; terminal cell have curved ends, which may ormay not be<br>tapering; curved ends of the terminal cells of a trichome both in the main filaments and the false branches; length varies from 4.9 to 7.6 μm, while the width ranges from 8.6 to 9.1 μm; heterocytes appear solitary and never in pairs; long and cylindrical with concave and convex ends; colour of the heterocytes is usually yellowish; position of the heterocytes is usually intercalary; length varies from 7.8 to 15.2 μm, while the width ranges from<br>8.7 to 9.7 μm. Akinetes not observed.','Saraf et al. 2018',NULL,0,0),(1532,1945,'description','Fäden einzeln, bis 18 mm lang. 8-12 trochome enthaltend, 50-86 um breit. Trichome 4-5 um breit. Zellen bis 5mal kürzer als breit. Scheiden farblos, fest, leicht geschichtet, halb so breit wie fie Fäden.','Reinsch ex Geitler 1932',NULL,0,0),(1533,1946,'description','Stratum atro-purpureum, floccosum, variis Algis affixum. Vaginae crassiusculae, demum omnino diffluentes. Trichamata pallide rubro-violacea, intra vaginam plus minusve numerosa, flexilia, apice frequenter arcuata, ad genicula eximie constricta (in speciminibus siccis), 8 um ad 12 um crassa; articuli diametro trichomatis duplo ad quadruplo breviores, 2 um ad 4 um longi; dissepimenta irregulariter granulata; apex trichomatis attenuatus, obtusus.','Gomont 1892',NULL,0,0),(1534,1949,'description','Stratum luteo-fuscum aut sordide vel luteo-virescens, haud caespitosum, mucosum, indefinite expansum, aut thallus cylindraceus. Vaginae ambitu valde irregulares et subamorphae, demum omnino diffluentes. Trichomata pallide virescentia aut fuscescentia, ad genicula non constricta, 14 um ad 21 um, vulgo 17 ad 19 um crassa; articuli diametro trichomatis triplo ad sextuplo breviores 2,5 um ad 3,5 um longi; dissepimenta granulata; apex trichomatis attenuato-truncatus.','Gomont ex Gomont 1892',NULL,0,0),(1535,1953,'description','Stratum corrugato-crustaceum, ad centimetrum crassum, griseum vel roseum vel aerugineum, calce impregnatum, filis longis gracilibus basi ramosis, passim caespitosis passim intertextis; vaginis cylindraceis gelatinosis hyalinis crassis multi-lamellosis, ambitu erosis, chlorozincico iodurato haud caerulescentibus, ad apices longe acuminatis; trichomatibus aerugineis vel luteolis, 4 um ad 8 um crassis, cylindricis, ad genicula non constrictis, ad apices abrupte attenuatis et truncatis, intra vaginas praecipuius solitariis raro duabus vel pluribus; articulis brevibus, praecipue 2-5-plo brevioribus, nonnumquam subquadratis, dissepimentis grosse-granulato, protoplasmate tenuigranuloso; cellula apicali depresso-hemisphaerica vel quasi-truncata, superne membranam incrassatam praebente.','Drouet 1943',NULL,0,0),(1536,1953,'etymology','named in honor of M. J. Groesbeck','Drouet 1943',NULL,0,0),(1537,1954,'description','Caespituli nigri, circiter quinque millimetra alti. Fila adnaa, abbreviata, inferne trunciformia, trunco brevi, a basi tenuiori apicem versus dilatato tune i laciniis diviso et repetite pseudo-ramoso, pseudo-ramis plus minusve divaricatis, flexuosis. Vagina subarctae, paulum mucosae, ambitu irregulares et erosae, in parte media filorum dilatatae, apicem versus longe attenuatae, acuminatae, apertae vel clausae, transverse corrugatae. Trichomata viridi-fusca, intra vaginam plura, arcte aggregata, recta, vel spiraliter implicatocontorta, interdum solitaria, ad genicula non constricta, 16 ad 19 um crassa; articuli brevissimi, diametro trichomatis triplo ad quintuplo breviores, 3,4 um ad 4,5 um longi, protoplasmate tenui-granuloso farcti; apex trichomatis levissime<br>attenuatus, vix capitatus, truncatus','Gomont ex Gomont 1892',NULL,0,0),(1538,1516,'description','Caespites fluctuantes, chalybeo-vel fusco-nigrescentes, indefiniti expansi. Fila simplicia &nbsp;aut parce pseudo-ramosa, flexuosa, plus minusve flexilia, fasciculato-implicata. Vaginae ]amellosae, subdiffluentes, cylindraceae, superficie erosae, transverse corrugatae, apice apertae aut acuminatae. Trichomata aeruginea vel chalybea, intra vaginam plura, parallela vel implicato-contorta, interdum solilaria, ad genicula haud constricta, 6 um ad 8 um crassa; articuli diametro trichomatis subaequilongi, vel eo ad duplo breviores, 4 um ad 5,5 um longi; dissepimenta frequenter granulata; apex trichomatis sublonge attenuatus, evidenter capitatus; cellula apicalis depresso-conica.','Kützing ex Gomont 1892',NULL,0,0),(1539,1957,'description','Caespite atro-viridi, vaginis diametro 1/300\'\' tenerrime membranaceis apice attenuatis, distincte trans- versim striolatis punctatitisque; filis inelusis plerumque binis vel ternis, fiexuosis, 1/600\'\' crassis, viridibus; articulis obsoletis diametro aequalibus.&nbsp;','Martens 1869',NULL,0,0),(1540,1958,'description','Lager <em>Phormidium</em>-artig, getrocknet fast schwarz. Fäden steif, gerade, 32 um breit. Scheiden eng, in den älteren Teilen bis 4 um dick, durch Chlorzinkjod sich nicht violett färbend, oft querfaltig, meist nur 1, selter 2-3 Trichome enthaltend, Zellen an den Querwänden nicht eingeschnürt, ca 28 um breit, sehr kurz. Endzelle nicht verjüngt und nicht kopfig-abgerundet.','Geitler 1932',NULL,0,0),(1541,1960,'description','Tapering heterocytous cyanobacteria found in freshwater and terrestrial habitats. No hair formation evident even after reducing phosphorous concentration. Morphologically similar to the genus Calothrix in having tapering trichomes but differing very clearly in habitat. 16S rRNA gene phylogeny clearly separates Dulcicalothrix from the morphologically similar genera <em>Calothrix</em>, <em>Rivularia </em>and <em>Macrochaete</em>.','Saraf et al. 2019',NULL,0,0),(1542,1962,'description','Bluish green macroscopic appearance in nature, found submerged in shallow water. Trichomes prominently tapering at one end with the broad base having a basal heterocyte. The attenuation is continuous and regular with the apical/distal ends being distinctly attenuated. Sheath surrounding the filament is colorless and has clear lamellation. Cells usually constricted at the ends with the older filaments having more prominent constrictions. Bow shaped necridia formation is the diagnostic feature of the species, oftenwith hormogonia formation adjacent to the necridia. Vegetative cells are wider near the basal heterocyte and continue to narrow towards<br>the distal end. In older filaments, width of the vegetative cells is prominently more than the length. In younger filaments the length of the vegetative cells is more than the width. Distal vegetative cells are 5.20–5.26 μm in length to 3.63–3.69 μm in width. Intercalary vegetative cells with sheath are 6.20–6.26 μm in length to 8.16–8.21 μm in width. Intercalary vegetative cells without sheath are 6.27–6.37 μm in length to 6.46–6.54 μm in width. Heterocytes are always basal and solitary with the shape being usually spherical although sometimes with a slightly elongated end. Basal heterocytes are 5.80–5.90 μm in length to 6.0–6.60 μm in width. Akinetes were not observed.','Saraf et al. 2019',NULL,0,0),(1543,1965,'description','Vaginis pollucidis arctis, 1/100 lin. crassis; filis internis fasciculatim contortis, 1/600 lin. crassis, obsolete articulatis; articulis diametro aequalibus, subgranulatis.','Martens 1871',NULL,0,0),(1544,1965,'etymology','named afte botanist Dr. René Lenormand','Martens 1871',NULL,0,0),(1545,1966,'description','Caespites nigro-virides, vel stratum rnucosum, late expansum. Fila adnata, basi simplicia, superne pseudo-ramosa, pseudo-ramis numerosis, subadpressis. Vaginae amplae, mucosae, ambitu erosae, ad apicem acuminatae aut saepius apertae, interdum omnino diffluentes et agglutinatae. Trichomata luteo-viridia, ad basim filorum numerosa et spiraliter implicato-contorta, in ramulis solitaria, ad genicula non constricta, 8 um ad 16 um, vulgo 9 um ad 11 um crassa; articuli diametro trichomatis triplo ad sextuplo breviores, 2,5 um ad 4,5 um longi; dissepimenta granulata; apex trichomatis attenuato-truncatus.','Kützing ex Gomont 1892',NULL,0,0),(1546,1968,'description','Lager büschelig, dunkelviolett. Scheiden eng, 3 oder mehr Trichome enthalted. Trichome violett, 4-5.5 um breit. Zellen bis 1/3 mal so lang wie breit. Endzelle kegilig-abgerundet.','Martens ec Geitler 1932',NULL,0,0),(1547,1968,'description','Caespite atroviolaceo; vaginis diametro 1/180 ad 1/150 lin., arctis, &nbsp;pellucidis; filis inclusis ternis v. pluribus, flexuosis, 1/360 lin. crassis, pallide violaceis, obsolete articulatis; articulis granulatis, diametro triplo brevioribus.','Martens 1871',NULL,0,0),(1548,1969,'description','Colonies are filamentous, with densely packed trichomes, blue-green, forming rough mats. Trichome was solitary or gathered in fascicles, straight or slightly curved, unbranched, narrowing toward the ends, constricted at the cross-wall, without a sheath. Vegetative cells were barrel-shaped, and apical cells rounded-pointed. Heterocyte cells were intercalary or terminal, spherical, sometimes elliptical, the width slightly larger than the length. Akinete cells were cylindrical (young) to elliptical (old), generally solitary on either side of the heterocyte cell, dark green with granular contents, smooth at surface, and were never found away from heterocyte cells.','Tawong et al. 2019',NULL,0,0),(1549,1970,'description','Colonies are filamentous, with densely packed trichomes, blue-green, forming rough mats. Trichome was solitary or gathered in fascicles, straight or slightly curved, unbranched, narrowing toward the ends, constricted at the cross-wall, without a sheath. Vegetative cells were barrel-shaped, 2.9–(3.92)–5.9 μm in length, 4.0–(4.78)–6.6 μm in width, L:W ratio 0.53–(0.84)–0.96, and apical cells rounded-pointed. Heterocyte cells were intercalary or terminal, spherical, sometimes elliptical, the width slightly larger than the length with 3.8–(5.0)–6.8 μm in length, 4.5–(5.6)–7.5 μm in width, and L:W ratio 0.77–(0.90)–1.00. Akinete cells were cylindrical (young) to elliptical (old), generally solitary on either side of the heterocyte cell, dark green with granular contents, smooth at surface, with 9.60–(13.4)–16.1 μm in length, 7.3–(9.3)–11.7 μm in width, L:W ratio 1.18–(1.46)–2.65, and were never found away from heterocyte cells.','Tawong et al. 2019',NULL,0,0),(1550,1973,'description','H. cespitulo fusco-viridi rigidulo, 1-3\'\' alto; vaginis crassiusculis monstruosis rigidis, basi fere setaceis, opacis, apice penicillatim divisis, hinc achromaticis, illinc fuscescentibus; trichomatibus internis 1/60\'\' crassis, fasciculatim contortis, obsolete articuJatis, pallide viridibus, non granulatis.','Kützing 1849',NULL,0,0),(1551,1973,'description','Strato caespituloso, fusco-viridi, rigidulo, 2-6 mm alto; vaginis subcrassis, monstrosis, rigidis, basi fere setaceis,<br>opacis, apice penicillatim divisis, hinc achromaticis, illinc fuscescentibus; trichomatibus internis 3-7 um crassis, fasciculatim contortis, indistincte articulatis, pallide viridibus, non granulatis.','Kützing ex Forti 1907',NULL,0,0),(1552,1976,'description','Strato verrucoso vel floccoso, olivaceo, muscos submersos arcte involventi; trichomatibus 3-4 um crassis, 2-10-nis, rarius singulis vel plurimis in fasciculos apice floccosos, 9-10 um diam. consociatis; articulis diam. 2-3-plo brevioribus; contentu aerugineo-viridi; vaginis plerumque arctis, sufficienter crassis, hyalinis, indistincte stratosis, superficie saepe opacis.','Hansgirg ex Forti 1907',NULL,0,0),(1553,1977,'description','Pulvinuli griseo-fuscescentes, calce indurati, durissimi, demum confluentes. Fila erecta, caespitosa, flexuosa, simplicia aut apice bifida. Vaginae amplae, ambitu irregulares et erosae, lamellosae, subdffluentes, apice nunc acuminatae, nunc dilatato-ochreatae et evanescentes. Trichoma pallide luteo-viidia, intra vagiam plra (usque ad sex), laxe aggregata et spiraliter intricato-contorta aut soliaria, ad genicula non constricta, cicier 6 um crassa; articuli inaequilongi, diametro trichomatis longiores aut usque ad duplo breviores, 3 um ad 9 um longi, protoplasmate grosse granuloso farcti; apex trichomatis sublonge attenuatus, evidenter capitatus; cellula apicalis depresso conica.','Braun ex Gomont 1892',NULL,0,0),(1554,1980,'description','H. cespite unciali saturate ærugineo, fasciculis apice attenuatis, cum vaginis ad 200 um crassis; trichomatibus multis subparallelis in vagina communi apice clausa crassa demum fuscencenti inclusis, 4—4 1/2 um crassis, apice paullulum attenuatis obtusis, obsolete articulatis, articulis diametro 3-5-plo longioribus, geniculis interdum paullum contractis (præcipue apicem versus) cytioplasmate granulis nonnullis submagnis sparsis repleto. Fortasse ad genus Sirocoleum Kütz. pertineat.&nbsp;','Nordstedt in Wittrock &amp; Nordstedt 1889',NULL,0,0),(1555,1981,'description','Strato rubro-fuscescenti, expanso; trichomatibus plerumque ad 12 um diam., aerugineis vel aerugineo-fuscescentibus, saepius singulis nonnunquam geminis vel ternis, rectis vel leviter contortis, aequalibus; articulis diam. 2-3-plo brevioribus, irregulariter granulatis; vaginis plantae vivae angustis, achrois, pellucidis, aetate provecta amplis saepe distincte lamellosis, firmis, pulchre luteo-fuscis, superficie levissimis, 20-25 um crassis; apice saepe conico.','Wolle ex Forti 1907',NULL,0,0),(1556,1983,'description','Lager olivenbraun bis schwarzbraun, matt glänzend, an vom Wasser berieselten Steinen und Felsen festgewachsen. Fäden zu halbkugeligen, rivularia-artigen, öfters geschichteten und zu einer bis 1/2 cm dicken festen Krust zusammenfliessenden Polstern vereinigt, einzeln, zu 2 oder mehreren in dünen Bündeln vereinigt, 1 bis 2 um breit, mit blass blaugrünem Inhalte, öfters fast calothrix-artig endigend; Zellen 1 bis 1 1/2 um breit, etwa 2mal so lang; Specialscheiden fast farblos, eng anliegend; gemeinsame Gallertscheiden gelblich gefärbt, 4 bis 6 um breit.','Hansgirg 1892',NULL,0,0),(1557,1985,'description','Filaments containing 1-5 trichomes, mostly straight, or somewhat tortuous, smooth, unbranched, narrow, spindle-form, closed at the apices when young, later the ends dissolving and the trichomes extruding; trichomes nearly parallel, separated from each other for the most part, moderately constricted at the dissepiments, acuminate at the apices; cells homogeneous, pale to bright aeruginous; cross-walls very thin; apical cell blunt-conical, with a very small calyptra; sheath ample, hyaline when young, changing to pinkish red at maturity, homogeneous.','Gardner 1927',NULL,0,0),(1558,1986,'description','Filaments solitary or in groups, not forming a compact thallus, not branched and probably not calcified. Sheaths fine, colourless, uneven from outside, containing several trichomes. Trichomes blue-green, not constricted at cross-walls, attenuated towards ends, about 6 μm wide. Cells usually shorter than wide, 3.5-6 μm long, granulated at cross-walls. Apical cells conical-rounded, with conical calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1559,1987,'description','Strato pelliculari-crustaceo, 1-3 mm. crasso, saepe calce valde incrustato et solido, laevi vel verrucoso-irregulari, brunneo-rufo, sectione sordide aerugineo-viridi; filamentis 2-10 consociatis, 3-4 um diam., rarius singulis vel pluribus parallele decurrentibus, sursum scandentibus, vagina singula circumfusis, in fasciculos 15-45 um<br>diam. consociatis; cellulis subquadratis vel diametro dimidio brevioribus, ante divisionem diam. sesquilongioribus, contentu aerugineo vel olivaceo, rarius pallide rufis; vaginis specialibus parum incrassatis, arcte instantibus, apicem versus leviter incrassatis; trichomatibus apice nudis, radiatim dispositis.','Hansgirg ex Forti 1907',NULL,0,0),(1560,1988,'description','Filaments with one to several trichomes in sheaths; sheaths cylindrical, lamellated, slightly diffluent; trichomes pale blue-green, not or very slightly constricted at cross-walls, 3.9-7.5 μm wide; cells 1.5-5.5 μm long, apical cells depressed-conical or almost rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1561,1992,'description','Filaments solitary, curved, 28-50 μm wide, up to 2 mm long; sheaths colourless, with transversal constrictions, when old almost diffluent, containing 1-2(3) trichomes; trichomes 6-6.3 μm wide, not constricted; cells nearly isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1562,1136,'description','Stratum obscure aerugineum. Fila fluexuosa, fragilia. Vaginae hyalinae, firmae, tenues, chlorozincico iodurato non carulescentes. Trichomata pallide aruginea, extra vaginam rectissima, ad genicula haud constricta, apice interdum capilala, 4 um ad 6 um crassa; articuli diametro trichomatis subaquilongi vel eo ad duplo breviores, 2,3 um ad 3 um longi; protoplasma crassis granulis dissepimenta frequenter obducentibus conspersum; dissepimenta haud raro granulata; cellula apicalis superne depresso-conica vel rotundata, membranam leviter incrassatam praebens.','Gomont 1892',NULL,0,0),(1563,1570,'description','P. trichomatibus aerugineis et flexuosis, apicibus saepe subattenuatis; cellulis subquadratis vel diametro paullo brevioribus. Crass, fil. 9.5-19 um; crass. trich. 4.5-5.5 um.','West et West 1897',NULL,0,0),(1564,1994,'description','Trichomes in free-swimming, spindle-like, to 2 mm long fascicles, consisting of 20-30 trichomes; trichomes cylindrical, slightly coiled, dark reddish, 6.3-7.7 μm wide, not attenuated at the ends; cells up to 2x longer than wide, apical cells rounded or obtuse, without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1565,1995,'description','Trichomes solitary, coiled, not constricted at cross-walls, cells longer than wide, 4-6.5 μm wide (but in Umezaki 1974 very short), with thin slimy envelopes.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1566,1612,'description','Fasciculi brevissimi , vix ad millimetrum longi, purpureosanguinei (sec. Ehrenberg), in speciminibus siccis griseovirides vel fuscescentes. Trichomata recta, parallela, ad genicula constricta, tenuiora apice sublonge attenuata, &nbsp;crassiora brevissime, 7 um ad 11 um, rarius ad 21 um crassa; articuli diametro subaequilongi vel eo ad triplo breviores, 5,4 um ad 11 um longi, protoplasmate grosse granuloso farcti.','Ehrenberg ex Gomont 1892',NULL,0,0),(1567,1997,'description','Fasciculi duo ad quinque millimetra longi, in speciminibus siccis luteo-fusci vel fusco-virides. Trichomata ad genicula haud constricla, apice breviter attenuata, 13 um ad 22 um crassa; articuli diametro trichomatis semper et usque ad triplo breviores, protoplasmate tenui-granuloso vel homogeneo farcti.','Gomont 1892',NULL,0,0),(1568,1998,'description','Fascicles with ± parallel arranged trichomes, 50-100 μm wide, 650-900 μm long, free-floating, blue-green, rarely in solitary filaments. Trichomes straight or slightly curved, pale blue-green, (5)7-8(9.5) μm wide, cylindrical, strongly constricted at the cross-walls, not or sometimes very slightly attenuated at the ends. Cells 2-5 μm long, shortly barrel-shaped, cell content with aerotopes. Apical cells not lengthened, nearly hemispherical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1569,913,'description','Fascicles with ± parallel arranged trichomes, 50-100 μm wide, 650-900 μm long, free-floating, blue-green, rarely in solitary filaments. Trichomes straight or slightly curved, pale blue-green, (5)7-8(9.5) μm wide, cylindrical, strongly constricted at the cross-walls, not or sometimes very slightly attenuated at the ends. Cells 2-5 μm long, shortly barrel-shaped, cell content with aerotopes. Apical cells not lengthened, nearly hemispherical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1570,909,'description','Fäden gerade, ungleich lang, annähernd parallel, zu Bündelchen von gegen 200 um dicke und bis 1000 um Lange und von hellbräunlichgelber Farbe vereinigt. Zellen meist kugelig tonnenförmig, stark abgerundet, mit flachen Wänden aneinander grenzend, 5-6 um dick, meist 3-6 um lang, Endzellen der Fäden mitunter mehr cylindrisch und verlängert, bis 12 um und dabei etwas verjüngt. - Die Verbindung der Fäden miteinander in den Bündeln ist eine sehr lockere; sie scheinen zwar durch etwas Gallerte zusammengehalten zu werden, doch ist diese so minimal, dass, wenn man die Alge in zerriebene Tusche legt, die Tuschetheilchen bis fast unmittelbar an die Zellen vordringen. Die Zellen enthalten Gasvacuolen; letztere sind in den Zuckerpräparaten weniger gut haltbar als die von Gloiotrichia oder Anabaena. Durch Behandlung der Zellen mit Alkohol und Haematoxylin treten, ähnlich wie bei Gloiotrichia, intensiv gefärbte Körner hervor, die zu einer centralen Gruppe vereinigt sind.','Klebahn 1895',NULL,0,0),(1571,2000,'description','Gallertlager linsenförmig 450—700 gross. Zellen ca. 8 um dick und 4-7 um lang. Endzelle haubenförmig. Inhalt der Zelle vakuolenreich.','Lemmermann 1899 (as Haliarachne lenticularis)',NULL,0,0),(1572,2000,'description','Trichomes radially-arranged forming free-floating colonies, 450-700 μm in diameter; trichomes about 8 μm wide, constricted at cross-walls; cells 4-7 μm long, apical cells with calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1573,2002,'description','Trichomes arcuated or slightly wavy, arranged radially in star-shaped colonies, 6-9(-11?) μm wide, constricted or unconstricted at cross-walls, cells longer than wide, blue-green or reddish, with aerotopes. Terminal cells widely rounded, without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1574,2003,'description','Fasciculis brevissimis ad 5 mm longis, siccitate fuscis: trichomatibus rectis ad genicula haud constrictis, apice rotundatis haud attenuatis, 9- 10 um crassis; articulis diametro trichomatis, 3 plo- brevioribus, contentu tenuigranuloso farctis, dissepimentis non aut vix granulatis. - An Oscillatorian consisting of bundles of trichomes, apparently the shortest in the genus, not more than 0.5 mm long. Colour when preserved in formalin dusky brown. Trichomes straight, not constricted at the genicula, nor attenuated toward the apex, 9 or 10 um thick, the articuli one-third the width of the trichome, with a finely granular content. Apices rounded, hemispherical, without calyptra. Dissepiments nearly or quite clear.','Lucas 1919',NULL,0,0),(1575,2004,'description','Trichomes in free-swimming fascicles, ± straight, partly rope-like contorted, or radially-arranged (“star-like”), blue-green or brownish-green when dried, 7-16 μm wide, not constricted at the cross-walls, briefly attenuated at the ends. Cells up to 2x as long as wide, sometimes nearly isodiametric, 8-26 μm long. Apical cells rounded, rounded with thickened cell wall (narrow calyptra?), or slightly widened and rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1576,2004,'description','Fasciculi ad sex millimetra longi, in specimiibu siccis fusco-virides. Trichomata i media parte fasciculorum funiformi-contorta, extremum versus soluta, ad genicula haud constricta, apice breviter attenuata aut iterdum inflata, 7 um ad 1 um crassa; articuli diametro trichomatis ad duplo longiores, rarius subquadrati, 8 um ad 26 um Iongi, protoplasmate grosse granuloso, dissepimenta saepe obducente farcti.','Gomont 1892',NULL,0,0),(1577,2005,'description','Filaments long, pseudobranched, developed to felt-like, incrusted, calcified, blue-green thallus among other algae. Sheaths thick, lamellated, firstly hyaline, later inside or entirely dark brown, containing one or two or more trichomes. Trichomes blue-green, 4-5 μm wide, straight or flexuous, not or slightly constricted at the cross-walls, long-attenuated at the ends. Cells 1/2-1/3x shorter than wide; cells content granulated. Apical cells long-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1578,2008,'description','Lager dünn, ziemlich fest, fast krustenförmig, schwärzlichbraun oder schmutzig rothbraun. Fäden meist gekrümmt. 4 bis 6 um dick, einzeln, zu 2 oder mehreren, oft fast parallel verlaufend, in einer 10 bis 50 um dicken, oft deutlich geschichteten, goldgelben, rosenrothen oder bräunlichen, selten farblosen, an den Enden offenen Gallertscheide eingeschlossen. Veget. Zellen ebenso oder 1/2 so lang, seltener etwas länger als breit, mit blass blaugrünem Inhalte.&nbsp;','Hansgirg 1892',NULL,0,0),(1579,2007,'description','Thallus thin, expanded, nearly leathery, blackish brown. Filaments pseudobranched. Sheaths thick, up to 10 μm wide, lamellated, yellow, rarely colourless, containing one to several trichomes. Trichomes pale blue-green, about 5 μm wide, sporadically (in parts) constricted at the cross-walls. Cells &nbsp;± &nbsp;isodiametric to 1/2x as long as wide. Apical cells rounded-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1580,2009,'description','S. minuta, flexuosa, curvula; vagina crassa, molli, aurantiaca, longitudinaliter striolata; trichomatibus internis viridibus solitariis vel binis parallelis, hinc moniliformibus, 1/700-1/60\'\' crassis, illince cylindricis, 1/500\'\' crassis, apice attenuatis, interdum exsertis.','Kützing 1849',NULL,0,0),(1581,2011,'description','Stratum pannosum fragile, aerugineum vel decoloratum, filis primum unitrichomatiferis tortilibus inter varias myxophyceas crescentibus, demum basin pluritrichomatiferis rectis et supra fastigiato-ramosis, ramis longis tortilibus trichomata praecipuius solitaria includentibus; vaginis hyalinis arctis demum crassioribus atque obscure lamellosis, ambitu erosis, chlorozincico iodurato caerulescentibus; trichomatibus pallide aerugineis vel viridi-aerugineis, 2 um ad 5 um crassis, cylindricis, ad genicula non constrictis, ad apices brevi-attenuatis; articulis quadratis vel diametro usque duplo longioribus, protoplasmate sparse tenui-granuloso, dissepimentis pellucidis; cellula apicali truncato-conica.','Drouet 1943',NULL,0,0),(1582,2012,'description','Thallus forming a blue-green phormidioid mat on agar, spreading onto dry glass; fascicles visible without &nbsp;magnification, very rarely producing upright tufts (Fig. 2). Filaments mostly with two to three trichomes, infrequently with more (up to 12) trichomes (Figs 11–15); trichomes frequently parallel in fascicle-like bundles (Figs 12, 15, 36) but not forming true fascicles in a common &nbsp;sheath, 4.5–16–(24) um wide. Sheaths common, open, colorless, often lamellate with lengthwise striation (Fig. 33), rarely with crosswise striation, sometimes irregularly widened, wavy or constricted. Trichomes slightly motile in exponential phase of growth, straight or curved, not to slightly constricted, more constricted in wider portions of trichome, sometimes with granulation at the crosswalls in exponential phase, slightly tapering to apices, with simple fragmentation common, rarely with necridia, which were most common in exponential phase, 3–3.5 um wide in exponential phase of growth, becoming up to 4 um wide in stationary phase. Hormogonia short, with as few as two cells when first formed (Figs 34–36). Cells longer than wide, up to three times longer than wide, with phormidiacean cell division, with fasciculated thylakoids evident (Figs 32, 33, 35, 37, 38), infrequently granular in the centroplasm, 4–9–(11) um long. Apical cells conical and longer than wide when mature, bluntly rounded (Figs 34, 35), tapering to a point (Figs 36, 38), or with a small irregularity (Figs 32, 37), often slightly brownish, 4.5–11 um long, 2.5–3 lm wide.','Pietrasiak et Mühlsteinová in Pietrasiak et al. 2014',NULL,0,0),(1583,2012,'etymology','Named in honor of our mutual colleague and friend, Valerie R. Flechtner','Pietrasiak et Mühlsteinová in Pietrasiak et al. 2014',NULL,0,0),(1584,2013,'description','Thallus forming a blue-green phormidioid mat on agar with nodules and coils of spiraled filaments, developing numerous pointed tufts of filaments up to 1 mm above the agar in the 6 mo after transfer (Fig. 3). Filaments with one to three trichomes, mostly parallel (Figs 16–19), with filaments containing spirally twisted trichomes present throughout the life cycle (Figs 20, 21, 39), 4.5–7–(18) um wide. Sheath commonly present, open, colorless, often lamellated with lengthwise striation (Fig. 47), more rarely with crosswise striations (Fig. 17), wavy or &nbsp;onstricted, rarely irregularly widened (Fig. 16). Trichomes motile throughout life cycle, not constricted at the cross-walls (Figs 16–20), or rarely slightly constricted (Figs 41, 42), slightly tapering to apices (Figs 41, 42, 44), with simple fragmentation common, rarely with necridia, which were most common in exponential phase of growth, 2–3 um wide in exponential growth, becoming up to 3 lm wide in stationary phase. Hormogonia short, with as few as two cells when first formed (Fig. 45). Cells slightly longer than wide to up to four times longer than wide, with phormidiacean cell division, with fasciculated thylakoids evident (Figs 39, 41–47), infrequently granular in the centroplasm, (3.5)–4–11–(12) um long. Apical cells conical and longer than wide when mature, infrequently bluntly rounded (Fig. 43), more commonly tapering to a point (Figs 44–46) or with a small nipple or irregularity (Figs 40, 41, 47), often slightly brownish in stationary phase (Fig. 21), 4.5–11 lm long, 2–3 um wide.','Pietrasiak &amp; Johansen in Pietrasiak et al. 2014',NULL,0,0),(1585,2013,'etymology','Torsivum (Latin) = spirally twisted.','Pietrasiak &amp; Johansen in Pietrasiak et al. 2014',NULL,0,0),(1586,2014,'description','Filaments long and sometimes tapering; usually uniseriate, sometimes multiseriate. Sheath present, colorless, thin (rarely thick), or at times not present. Trichomes slightly to strongly constricted at cross walls. Heterocytes present, intercalary, basal, or apical. Displays ‘T’ type branching. Akinetes present, in series, with granular cytoplasm and thick epispore, separating this genus from most other Hapalosiphonaceae.','Casamatta et al. 2020',NULL,0,0),(1587,2015,'description','Thallus consisting of densely entangled fibers, forming a thick, forest green mat on bottom of liquid culture flask, occasionally detaching and forming a floating surface layer. Filaments mostly uniseriate, sometimes biseriate, brown, grass green, or blue green with cell growth in multiple planes of division. Trichomes constricted at the cross walls, sometimes strongly, when actively growing not or only slightly constricted, sometimes tapering apically, main axis 7.5–17 um wide, branches tapering to 3.75–5 um wide at apices. Sheaths colorless, very thin, often not apparent. Cells variable in size; shorter than wide in main axis, becoming longer than wide in branches, apical cells in branches longer and tapered, as opposed to the wider, isodiametric, globose basal cells. Heterocytes basal, apical, or intercalary, when intercalary forming to the side of the main axis, 5–6 um wide, 4–5 um long. Akinetes oval to spherical, thick walled, forming in series, with granular brown contents, germinating perpendicular to the axis of the filament, 5–13 um wide.','Casamatta et al. 2020',NULL,0,0),(1588,2016,'diagnosis','Fila agglutinata, interdum parallele disposita, fasciculos prostratum, ferrugineo-castaneis usque nigro-castaneis; filamentis flexuosis cum 1 trichoma, 12.2-16.0 um diam.; vaginae crassiusculae, homogeneus vel cum parallele lamellae, hyalinae usque aurantiaco-ferrugineis, interdum coalescentes, trichomatibus abusque constrictis, genicula non visibili, 8.510.5 um diam.; articulis (3.0)4.0-7.0 um longis usque 0.8 longiores quam latiores, protoplasma granulatum, caerulescentes; cellula apicalis rotundata conica usque acute conica.','Branco et al. 2006',NULL,0,0),(1589,2017,'diagnosis','Fila parallele disposita, coalescente, fasciculos prostratum, caerulescentes; filamentis non ramosis cum 1 trichoma, 8.0-12.0 um diam.; vaginae apice apertus, homogeneus vel lamellosae, hyalinae usque luteo-casteneis, trichomatibus constrictis, 8.0-9.0 um diam.; articulis 3.0-7.0 um longis, 1.1-2.2(2.6) &nbsp;latiores quam longiores, protoplasma granulatum, caerulescentes; cellula apicalis rotundata cylindricis vel rotundata conica.','Branco et al. 2006',NULL,0,0),(1590,2018,'diagnosis','Fila agglutinata, fasciculos erectis, usque ad 2mm elatis, nigro-ferrugineis usque aurantiaco-ferrugineis; filamentis ramosis cum 1 trichoma, interdum 2 vel 3 trichomatibus, 12.0-19.0 um diam.; vaginae apice clauso, lamellosae, hyalinae usque aurantiaco-ferrugineis, trichomatibus constrictus, 3.2-3.6 um diam.; articulis 3.6-6.0 um longis, 1.1-2.0 longiores quam latiores, protoplasma granulatum, chromatoplasma visibili, caerulescentes; cellula apicalis rotundata cylindricis.','Branco et al. 2006',NULL,0,0),(1591,2020,'description','Thallus membranaceous, dark dirty reddish or greenish, with ± parallelly-arranged filaments. Sheaths colourless, wide; filaments 5.6-11 μm wide. Trichomes not constricted at cross-walls (?), 2.2-4.5 μm wide. Cells ± &nbsp;isodiametric, or slightly longer than wide.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1592,1605,'description','Strato indefinite expanso, nigro vel olivaceo-chalybeo; filis inferne tortuosis et intricatis, superne subrectis, parallelis, in lacinias adpressas subdichotome divisis et pseudoramosis, fasciculos rigidos, erectos, spiniformes, ad 3 cm. altos formantibus; vaginis cylindricis, firmis, apice acuminatis, lamellosis, levibus aut ambitu paulum erosis, chlorozincico jodurato caerulescentibus; trichomatibus dilute aerugineis, intra vaginam paucis vel solitariis, parallelis, ad genicula evidenter constrictis, 3-6 um crassis; articulis diam. trichomatis subaequilongis vel eo usque 2-plo longioribus, 4-11 um longis, cunctis (apicalibus exceptis) contentu grosse granuloso farctis; rellula apicali truncato conica.','Forti 1907',NULL,0,0),(1593,2021,'other','','',NULL,0,1),(1594,559,'description','Fila in stratum indefinitum, expansum, fusco-vel viridiatrum intricata, aut fasciculos decumbentes muscis affixos formantia, aut libere natantia, elongata et modice flexuosa, in laciniis adpressis divisa el pseudo-ramosa. Vaginae luteo-aureae, firmae aut subdiffluentes, ambitu irregulares, apice acuminatae, chlorozincico iodurato caerulescentes. Trichomata aeruginea, intra vaginam pauca, interdum solitaria, ad genicula leviter constricta, 7 um ad 13 um crassa; articuli diametro trichomatis ad duplo breviores vel eo paulo longiores, 4 um ad 9 um longi, proloplasmate grosse granuloso farcti; cellula apicalis obtuse conica.','Gomont 1892',NULL,0,0),(1595,2022,'description','Thallus crusty, hard, thick, calcified, blue-green on the surface, colourless inside. Sheaths thin, colourless, firm. Trichomes coiled, blue-green, very slightly constricted at cross-walls, 4-7 μm wide. Cells &nbsp;± &nbsp;isodiametric or slightly shorter than wide, usually slightly constricted at cross-walls.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1596,547,'description','Stralum molle, nigro viride. Fila flexuosa, in fasciculos fluctuantes apice penicillatim divisos arcte implicata, simplicia aut subsimplicia. Vaginae non lamellosae, chlorozincico iodurato non caerulescentes, inferne crassiusculae, ambitu irregulares et erosae, frequenter teansverse plicatae, superne arctae, cylindraceae. Trichomata aeruginosa, ad genicula haud constricta, plerumque intra vaginam solitaria, in parte autem inferiore filorum duo vel plura, 2,7 um ad 5 um crassa; articuli diametro trichomatis paulo breviores vel ad duplo longiores, 2 um ad 9 um longi; dissepimenta feequenter irregulare granulata; cellula apicalis obtuse conica.','Gomont 1892',NULL,0,0),(1597,2024,'description','cespite obscure aerugineo; trichomatibus rigidiusculis, aerugineis, 1/700- 1/650\'\' &nbsp;in fasciculos apice penicillatim solutos implicatis contortisque, ad genicula transversim punetatis, vaginis subtilibns laevissimis, plerumque inconspicuis.','Kützing 1847',NULL,0,0),(1598,558,'description','Stratum indefinilum, expansum, atro-violaceum. Fila modice elongata, in laciniis plus minusve divaricatis subdichotome divisa et pseudo-ramosa, inferne intricata, superne sub parallela et faciculos tortuosos repentes fomantia. Vaginae purureo-aurantiaca vel rosea apice hyalinae, fimae soldae, crassissima eteximie lamellosae, ambitu irregulares et erosae, apice acuminatae, chlorozincico iodurato caerulescentes. Trichomata pallide aeruginea, intra vaginam numerosa, paulum remota et paallela, ad genicula vulgo constricta, 6 um ad 8 um crassa articuli diametro trilchomatis subaequilongi, aut eo ad duplo breviores, 3 um ad 8 um longi, omnes, apicalibus exceptis, protoplasmate grosse granuloso farcti; cellula apicalis conica, saepe acutissima.','Gomont 1892',NULL,0,0),(1599,2026,'description','Thallus small, spherical, epiphytic. Sheaths thick, colourless, 2.7-4.5 μm wide. Trichomes 2.5-6 μm wide, granulated at the cross-walls. Cells 1/2-1/3x as long as wide. Apical cells?','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1600,2027,'description','Plants forming slender symplocoid fascicles coalescing more or less at the base and about 5 mm high; filaments branching more or less freely at the base but simple above throughout the greater portion of their length, containing 1-3 trichomes at the base and but a single one above, intertwined and closely appressed, forming acute fascicles, 15-20 um diam. above in the unbranched portion, with closed, acute apices; trichomes constricted at the cross-walls; cells cylindrical, homogeneous to densely granular, aeruginous, 3.7-4 um. diam., 2-4.5 times as long as the diam.; apical cell blunt rounded, not capitate; sheath hyaline, homogeneous.','Gardner 1932',NULL,0,0),(1601,2029,'description','S. bryophila, late expansa, griseo-lutea; fasciculis erectis, angustis subulatis, aggregatis (passim densis), 8-15 mm altis, aeruginescentibus; trichomatibus aerugineis, flexuoso-intricatis, in strato strictioribus, apicibus versus fasciculorum, 1-3 in lata vagina inclusis, saepe interruptis, distincte articulatis; articulis diametro 2-4 plo longioribus; vaginis amplis, achrois, pellucidis vel interdum stratis parallelis formatis, in ambitu saepe subrugosis, apice angustioribus et saepe ramosis. Diam. trich. (s. vag.) l.9-2.3 um; crass, trich. c. vag. 13.5-25 um.','West &amp; West 1894',NULL,0,0),(1602,2031,'other','Strato expanso, aeruginoso, parce fasciculos 1 mm altos ostendentibus; filis 4-4,5 um diam., laxe intricatis; trichomatibus maxime torulosis, 3-3.5 um diam.; cellulis quadratis, cellula terminali rotundata nec capitata nec calyptrata; cytioplasmate homogeneo, dilute aerugineo; dissepimentis obscuris; vaginis tenuibus, hyalinis, strictis, primo levibus demum exteriore asperis. &nbsp;Filaments 4-4.5 um diam., forming an aeruginous stratum of erect, &nbsp;loose fascicles, 1 mm high; trichomes decidedly torulose, 3-3.5 um diam.; cells quadrate, terminal cell much rounded, neither capitate nor calyptrate; protoplast homogeneous, pale aeruginous, dissepiments &nbsp;obscure; sheath very thin, colorless, close, at first smooth, later becoming roughened on the outside.&nbsp;','Gardner 1918',NULL,0,0),(1603,2032,'description','Fasciculato caepitosa, nigro-viridis. Fasciculi erecti, ad centimetrum alti. Fila densissime implicata, libera, simplicia, valde et angulose torluosa. Vaginae tenues, firmae chlorozincico iodurato caerulescentes. Trichomata viridiluteola, 4 um ad 6 um crassa, per totam longitudinem ad genicula constricta; articuli vulgo quadrati aut diametro breviores, rarius longiores, 2 um ad 6 um longi; protoplasma vix granulosum; dissepimenta conspicua, pellucida, haud granulata; membrana celluloe apicalis in calyptram depressoconicam superne incrassata.','Gomont 1892',NULL,0,0),(1604,2033,'description','S. pulchre as laete aerugineo-cyanea, fasciculis aggregatis, tres, quatuor lineas ad pollicem usque altis, a basi lata sublamelliformi acuminatis, apice saepius solutis subpenicilliformibus; trichomatibus subaequalibus, leviter curvatis, erectis, subparallelis, parum intricatis, raro interruptis, laete coeruleo-aerugineis, lucidis, muco matricali achroo laxe conglutinatis, humectatis valde lubricis, mucosis, sub luce obliqua distincte atriculatis, articularis diametro &nbsp;paulo longioribus, post divisionem factam dimidio brevioribus; cytioplasmate granuloso pulchre aerugineo; vaginis arctis, passim tumidis , homogeneis, laevissimis, achromacitis, superne saepe vacuis. Diam. s.v. 1/422-1/382´´´','Rabenhorst 1865',NULL,0,0),(1605,2034,'description','Lager dünn, ziemlich fest, fast krustenförmig, schwärzlichbraun oder schmutzig rothbraun. Fäden meist gekrümmt. 4 bis 6 um dick, einzeln, zu 2 oder mehreren, oft fast parallel verlaufend, in einer 10 bis 50 um dicken, oft deutlich geschichteten, goldgelben, rosenrothen oder bräunlichen, selten farblosen, an den Enden offenen Gallertscheide eingeschlossen. Veget. Zellen ebenso oder 1/2 so lang, seltener etwas länger als breit, mit blass blaugrünem Inhalte.&nbsp;','Hansgirg 1892',NULL,0,0),(1606,2037,'description','Stratum molle, nigroviride. Fila flexuosa, in fasciculos fluctuantes apice penicillatim divisos arcte implicata, simplicia aut subsimplicia. Vaginae non lamellosae, chlorozincico iodurato non caerulescentes, inferne crassiusculae, ambitu irregulares et erosae, frequenter transverse plicatae, superne arctae, cylindraceae. Trichomata aeruginosa, ad genicula haud constricta, plerumque intravaginam solitaria, in parte autem inferiore filorum duo vel plura, 2,7 um ad 5 um crassa; articuli diametro trichomatis paulo breviores vel ad duplo longiores, 2 um ad 9 um longi; dissepimenta feequenter irregulare granulata; cellula apicalis obtuse conica.','Gomont 1892',NULL,0,0),(1607,2023,'description','Thallus soft, expanded, dark green, greyish blue-green to dull blue-green, later incrusted, yellowish to fleshy, warty, uneven, outside rough, inside zonated. Filaments at the base entangled, at the ends ± parallelly-aggregated to ascending, penicillate fascicles (tufts), not or sparsely pseudobranched. Sheaths firm, distinct, colourless, not or sporadically lamellated, in the basal part thick and uneven, containing 2-3(5) or occasionally many trichomes, in the upper part thin, containing mostly only a single trichome. Trichomes blue-green, 2.4-5(6) μm wide, not or somewhat constricted at the irregularly granulated cross-walls. Cells shorter or up to 2x longer than wide, 2-9 μm long. Apical cells obtuse-conical or rounded-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1608,2025,'description','Thallus expanded, flat or sometimes cushion-shaped, black-red or violet to dark purple, rarely blackish brown. Filaments nearly dichotomously pseudobranched, in lower part entangled, in upper parts forming somewhat parallelly-arranged and twisted, creeping, up to 3 cm long tufts. Sheaths reddish to purple-red or red-orange, firm, at the ends (or in shade) colourless, pointed at the ends, thick, distinctly lamellated, outside uneven, acuminate at the ends, containing numerous trichomes, which are somewhat remote one from another and parallelly-arranged. Trichomes pale blue-green, (5)6-8 μm wide, usually constricted at the cross-walls. Cells 3-8 μm long, mainly ± isodiametric. Apical cells conical, often pointed.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1609,516,'description','trichomes solitary, later aggregated into macroscopic &nbsp;heap–like &nbsp;colonies, &nbsp;straight &nbsp;or &nbsp;slightly bent, more or less attenuated at the apical cells, trichome &nbsp;without &nbsp;mucilaginous &nbsp;sheath, &nbsp;motile, &nbsp;not &nbsp;or slightly constricted at the cross–walls, cells rectangu-lar or barrel–like, 5.25±0.79 μm wide, 4.32±1.04 μm long, cell content green, blue–green or pale blue–green with visible chromatoplasma (especially under labora-tory conditions), without granules at the cross–walls, trichomes divide into hormogonia via the formation of necridic cells. Species possesses radial arrangement of thylakoids on transversal plane. Thylakoids on longitu-dinal plane form skew–like structures.&nbsp;','Hašlet et al. 2014',NULL,0,0),(1610,516,'etymology','the species epithet is derived from attenu-ated ends of trichomes','Hašler et al. 2014',NULL,0,0),(1611,1846,'description','In reddish or blackish mats, trichomes 3.5- 5 μm wide, greyish to violet, not constricted at cross-walls, coils 9.5-18 μm wide, 14-24 μm high.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1612,1850,'description','Trichomes (solitary or in mats?), not constricted at cross-walls, 3.5-4(-5) μm wide; coils only 6-7 μm wide and 12-15 μm high; cells distinctly shorter than wide, 0.8-1.2 μm long, apical cells rounded without calyptra.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1613,2042,'description','Trichomes short, S‑like curved, 8‑12‑celled, 4 μm wide, distinctly constricted at the ungranulated cross‑walls, not tapered at the end. Cells nearly barrel‑shaped, shorter than wide, c. 2‑3 μm long, bright blue‑green. Apical cells widely-rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1614,2045,'description','Trichomes usually solitary among other algae, or in small clusters, pale steel‑blue, olive‑green, pale green to dark green, sometimes slightly violet, 11‑16 μm wide, very loosely, but ± regularly screw‑like coiled, strongly knotted and contorted, comparatively short, not constricted or very slightly constricted at the thin, distinct and ungranulated cross‑walls, not attenuated at the ends, without sheaths. Cells very short, discoid, 2.5‑4 μm long. Apical cells rounded to very convex, without thickened outer cell wall, without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1615,2046,'description','In nature, growing on the wet soil. Colonies usually purple to black, irregularly clustering, forming diffluent mucilage. In liquid media culture growing at-tached to the glass walls of the test tubes, filaments ag-gregated into macrocolonies (up to 1 mm in diameters). Filaments flexuous, freely entangled, sheath present or not, colorless. Vegetative cells purple, barrel–shaped to cylindrical. Heterocytes spherical or cylindrical, usu-ally develop in intercalary position, 1 to 3, trichomes divided in the position of heterocyte, leading to 1–3 heterocytes in terminal. Akinetes oval, varying in color from brown, green to purple,easily distinguished from vegetative cells, up to 10 μm long, up to 7 μm wide (average size 7.95 μm long and 6.12 μm wide), usually in short chains (1 to 8). Akinetes develop intercalarly, usually distant from heterocytes, occasionally appear between two heterocytes.','Cai et al. 2020',NULL,0,0),(1616,2047,'description','Colonies purple to black, forming diffluent mucilage. Filaments flexuous, freely entangled, sheath present or not, colorless. Vegetative cells barrel–shaped to cylindrical, 2.28–3.78–5.34 μm long, 2.66–3.36–4.2 μm wide. Heterocytes spherical or cylindrical, 2.79–3.71–4.92 μm long, 2.66–3.46–4.45 μm wide. Akinetes oval, brown, green to purple, 7.95 μm long and 6.12 μm wide.','Cai et al. 2020',NULL,0,0),(1617,2044,'description','','Komárek &amp; Anagnostidis 2005',NULL,0,1),(1618,2048,'description','Trichomes pale to dark blue-green, (2.5)3-4 μm wide, regularly coiled, not constricted at the ± visible cross-walls, slightly conical- attenuated at the ends; spirals (8)11-16 μm wide, distance between spirals 7-12(15) μm, apical cells ± conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1619,2049,'description','Fäden einzeln unter anderen Algen, kurz, zerbreehlich, gerade, ohne Schleimhülle, ohne Scheidewände, tief blaugrün mit körnigem Inhalt. Spiren 11-16 um breit, locker, regelmässig. Breite des Trichoms 3-4 um..','Schmidle 1902',NULL,0,0),(1620,2050,'description','The diameter of the trichome is from 2.5-3 um. It is regularly twisted into a rather lax spiral, the distance between the turns being 16-18 um and the width of the turn about 6 um. Caduceus forms are not uncommon. The cells of the trichome vary from 4-5 um in length; the cell divisions in vigorous trichomes are indistinct with few granules and with the cell contents light bluish green by transmitted light. In the majority of the cells large vacuoles are present.&nbsp;','Setchell 1895',NULL,0,0),(1621,1164,'description','Trichomata plus minusve saturate aeruginea, stratum tenue formantia aut &nbsp;inter alias Algas sparsa, fragilia, in spiram laxam, diametro 9 um ad 15 um aequantem contorta, frequenter in caducei figuram implicata, ad genicula haud raro subconstricta, apice aequalia, haud capitata, 5 um ad 8 um crassa; anfractus 21 um ad 31 um inter se distantes; articuli subquadrati aut diametro breviores, 4 um ad 5 um longi, protoplasmate vix granuloso farcti; dissepimenla interdum subtiliter granulata.','Stizenberger ex Gomont 1892',NULL,0,0),(1622,2051,'description','Trichomes solitary, free-floating, blue-green, regularly screw-like coiled, not attenuated towards ends, not constricted, 4.2-5.1 μm wide, coils 6.8-7.6 μm wide, 17-19.2 μm high; cells short, with aerotopes, apical cells rounded, without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1623,2052,'description','Trichomata planctonica in flore-aquae erescentia, aeruginea, in spiram laxam amplissimam diametro circa 20 um contorta, ad genicula haud constricta, ad apices leviter attenuata et subcapitata, 3 um ad 5 um crassa; anfractubus circa 20 um inter se distantibus; articulis brevibus, diametro 3-plo brevioribus usque ad subquadratis, dissepimentis granulatis, protoplasmate pseudovacuolas grandes continenti.&nbsp;','Drouet &amp; Stricland in Drouet 1942',NULL,0,0),(1624,2053,'other','Plant mass dark blue-green. Cells 2.5-2 um wide, in a very loose spiral. Width of spiral 6-4 um, distance between turns 20-15 um. Cells contents blue-green.','Smith 1916',NULL,0,0),(1625,1227,'description','Trichome meist 4zellig halbkreisförmig, oder S-förming gebogen, seltener 1-2 Windungen bildend. Zellen zylindrisch, schwach gebogen, 0.8-1 um breit, 3-6 um lang, schmutzig gelbgrünlich, an den Enden durch gegenseitigen Druck abgeplattet. Windungen 6-12 um, meist 9 um breit.','Geitler 1932',NULL,0,0),(1626,2055,'description','Die Fäden halbkreisförmig oder S- förmig gebogen, selten 1 - 2 Windungen bildend. Die Zellen cylindrisch, wenig gebogen 0,8 -1 um dick, 3 - 6 um lang, schmutzig gelbgrünlich, ohne Pseudovakuolen, an den beiden Enden flach. Windung 6 - 12, gewöhnlich 9 um breit, sehr flach. Am häufigsten bilden 4 Zellen einen Faden. Gallerthülle, Dauerzellen oder Heterocysten fehlen. &nbsp;','Raciborski 1910',NULL,0,0),(1627,1165,'description','Trichomata dilute aeruginea, inter varias Algas sparsa aut in stratum saturate aerugineum agglomerala, plus minusve fluxuosa, in spiram laxiusculam regularem, diametro 2,5 um ad 4 um aequantem contorta, 1,2 um ad 1,7 um crassa; anfractus inter se 2,7 um ad 5 um distantes.','Gomont 1892',NULL,0,0),(1628,2056,'description','Trichomes pale blue-green, 6-7 μm wide, constricted at the ungranulated and translucent cross-walls, not attenuated at the ends; coils 15-20 μm wide, distances between coils 60-70 μm; cell content scarcely granulated.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1629,2057,'description','Trichomes greyish blue-green or yellowish blue-green, 5-6 μm wide, regularly loosely screw-like coiled, not constricted at the cross-walls, to 350 (or more?) μm long; cells usually shorter than wide, with ± homogeneous content, without aerotopes. Apical cells rounded conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1630,2058,'description','Stratum arugineum, compactum. Trichomata dilute aruginea, flexilia, curvata, in spiram plus minusve laxam, subirregularem, diametro 3,2 um ad 5 um aquantem contorta, 1,2 um ad 1,8 um crassa; anfractus 3 um ad 5 um et ultra inter se distantes.','Gomont 1892',NULL,0,0),(1631,2060,'description','Trichomata aeruginosa, sparsa aut in stratum olivascens agglomerata, eximie recta, fragilia, ad genicula haud constricta, 4 um ad 6,5 um crassa, apice haud capitata subacute et breviter attenuata uncinata vel tortuosa, passim cellulis inflato-torulosis et refringentibus interrupta; articuli diametro trichomatis duplo ad triplo breviores, 1,5 um ad 2,8 um longi, protoplasmate tenui-granuloso farcti; dissepimenta non granulata; calyptra nulla.','Kützing ex Gomont 1892',NULL,0,0),(1632,2061,'description','Stratum subolivaceo-viride. Trichomata dilute aeruginosa, ambitu recta, fragilia, in spiram eximie regularem diametro 5 um aequantem contorta, 2 um crassa; anfractus inter se 5 um distantes.','Gomont 1892',NULL,0,0),(1633,2062,'description','Trichomatla pallide aeruginosa, in stratum saturate aerugineum aut aerugineo-lutescens agglomerata, vel inter varias Oscilliarieas sparsa, ambitu irregulariter tortuosa, rarissime recta, in spiram densam subirregularem, passim laxiusculam, aut rarius regularem, diametro 3 um ad 5 um requantem contorta, 1 um ad 2um crassa; an fractus contigui vel subcontigui.','Oersted ex Gomont 1892',NULL,0,0),(1634,2062,'description','Thallus soft, thin, flaky, ± expanded, mucilaginous, sometimes spotty, bright blue‑green, emerald green, olive‑green, dirty blue‑green to blackish, frequently also only in solitary trichomes among other cyanoprokaryotes. Trichomes pale to bright blue‑green, sometimes emerald green, occasionally yellowish or pale violet or reddish, (0.8)1‑2(2.2) μm wide, regularly densely screw‑like coiled (rarely with irregularities), straight or variously curved, sometimes circle‑like (spirally) coiled, not constricted at the ± invisible cross‑walls (in LM), 150‑500(‑700) μm long. Coils dextral, regularly tightly joined to one another, nearly parallelly-arranged, only exceptionally (especially at the trichome ends) somewhat irregularly loosely coiled and not attaching together, but in that case colourless or very pale blue‑green (pathological stage ?), 3‑5 μm wide, (2)3‑5(5.6) μm high, short to long; rapidly motile, with very intense right‑handed screw‑like rotation and simultaneous gliding. Apical cells rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1635,1244,'description','Trichomes pale blue‑green, free‑floating, solitary, cylindrical, with up to 27 cells, immotile, (1.2)2‑3 μm wide, ± regularly and distinctly screw‑like coiled (with maximum 8 coils), constricted at cross-walls, sometimes disintegrating in solitary cells. Mucilaginous envelopes up to 15 μm wide; the slime is colourless, diffuse, fine (staining!). Spirals (helices) (8)15‑16 μm wide, distance between spirals (5)12‑15 μm. Cells cylindrical up to long barrel‑shaped, arcuated, sigmoid, 2‑2.5x longer than wide, 5‑6.3(12) μm long, with homogeneous content. Apical cell rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1636,2065,'description','Trichomata aeruginea, stratum tenue saturate aerugineum formantia, fragilia, in spiram laxam et amplissimam, diametro 26 um ad 36 um aequantem contorta, ad genicula subconstricta, apice !eviter attenuata, haud capitata, 6 um ad 8 um crassa; anfractus 43 um ad 57 um inter se distantes; articuli subquadrati, vel diametro breviores, 2 um ad 6 um longi, protoplasmate grosse granuloso dissepimenta vulgo obducente farcti.','Gomont 1892',NULL,0,0),(1637,2066,'description','Cellulæ granulis repletæ, (latitudine 1/3-1/4 brevioribus; anfractibus laxis, distantia c. 30 — 50 um). Crassitud. 7 — 8 um.','Nordstedt in Wittrock &amp; Nordstedt 1884',NULL,0,0),(1638,2067,'diagnosis','Trichoma libere natantia, solitaria, sine vaginis vel involucris mucilaginosis distinctis, dense vel libere dextrorse et plus minusve regulariter helicoidales, cylindrical, ad apices not attenuate, ad dissepimenta not constricta, 2.8-3.8 µm lata; spirae longitudine equaliter, (8.8)-12.5-18.5 µm latae, 5.5-5.8 µm altae (sed ad 40 mm in trichomatibus libere torsis); dissepimenta tenua, paucim visibilia in microscopis opticis. Cellulae1-4 × 2.8-3.8 µm, contentu pallide aeruginoso, interdum cum granulis parvis ad dissepimenta locatis, cum vesiculis gaseosis facultativis; cellula terminalis rotundata, sine calyptra. Heterocytae akinetesque carentes.','Komárek &amp; Komárková-Legnerová 2007',NULL,0,0),(1639,2067,'description','Filaments (trichomes) solitary, free-floating, without sheaths, screw-like, densely or loosely righthanded (dextral) coiled, cylindrical along the whole length, not attenuated or tapered at the ends, not constricted at cross-walls; the width of coiling is the same along the whole trichome (not narrowed towards ends); trichome width 2.8-3.8 µm, width of coils (8.8-)12.5-18.2(-18.5) µm, height of coils (very variable) 5.5-5.8 (in densely coiled trichomes) up to 25-40 µm (loosely coiled trichomes). Cross-walls hardly visible (staining !), cells pale blue-green, ± isodiametric or shorter than wide after division (up to 1/3 of width), sometimes slightly granular at crosswalls, aerotopes not observed, but possibly gas vesicles are present; terminal cells widely rounded, without calyptra.','Komárek&nbsp; &amp; Komárková-Legnerová 2007',NULL,0,0),(1640,2069,'diagnosis','Trichomata solitaria, libere natantia, cylindracea, regulariter spiraliterque tortusa, ad dissepimenta haud constricta, apice not attenuata nec capitata; vaginae carentes; spirae 7.4-1 1.8 urn in diametro, 7.4-13 urn longae; cellulae cylindraceae, 3.1-9.3 x 3.1-4.3 urn, contentu homogeneo, aerugineo, dissepimenta distincta, haud granulata; cellula apicalis rotundata, not incrassata; vesiculi gaseosi carentes','Margin et al. 1997',NULL,0,0),(1641,2069,'etymology','Named to the honor of Dr. H. Skujae','Margin et al. 1997',NULL,0,0),(1642,2072,'description','Stratum mucosum, sordide virescens. Trichomata agglutinata, dilutissime viridia, luteola, flexuosa, in spiram eximie regularem, diametro 1,5 um ad 2,5 um aequantem contorta, 0,6 um ad 0,9 um crassa; anfractus inter se 1,25 um ad 2 um distantes.','Kützing ex Gomont 1892',NULL,0,0),(1643,2074,'description','Stratum tenue, mucosum, nigro-purpureum. Trichomata in speciminibus vivis purpureo-violacea, passim aeruginosa (sec. auct.), in siccis omnia aeruginosa, flexilia, ambitu recta aut subrecta, in spiram densam regularem) diametro 3 um ad 4.4 um aequantem contorta, 1,2 u. ad 1,8 um crassa; anfractus contigui.','Cohn ex Gomont 1892',NULL,0,0),(1644,2078,'description','Fila flexuosa. Vaginae mucosae, agglutinantes. Trichomata olivaceo-viridia, intra vaginam numerosa, in fasciculos apice acuminatos, funiformi-contortos arcte aggregata, undulata, ad genicula constricta (in speciminibus siccis), apice longe attenuata, 9 um ad 11 um crassa; articuli diametro trichomatis duplo ad triplo breviores, 3,5 um ad 5,5 um longi, protoplasmate tenui-granuloso farcti; dissepimenta granulata? ; cellula apicalis haud capitata, acutissime conica.','Gomont 1892',NULL,0,0),(1645,2080,'description','Filaments small and relatively straight, 400-550 um long, 20- 35 um diam., containing 15-30 trichomes, closed at the conical tips when young, later opened and the trichomes extruding; trichomes straight, almost parallel in the sheath, not constricted at the cross-walls, long and very sharply acuminate at the apices; 1.8-2.2 um diam.; cells pale aeruginous, homogeneous, 2-4 times a s long as the diam.; apical cell longer and very sharp, conical; cross-walls obscure; sheath hyaline, irregular along the margin, somewhat mucous.','Gardner 1927',NULL,0,0),(1646,2081,'description','Microcoleus aquaticus, strato serugineo-chalybeo, trichomatibus aequalibus in fasciculos filiformibus, articulis diametro subaequalibus vel paullo brevioribus, subtiliter &nbsp;granulatis, apiculo subobtusis vel obtuso-rotundatis; vagina universali crassa, undulato-constricta et transversim striata [ut in <em>Symphyosiphoni Thelephoroidi </em>(Mon-tagne), Rabenhorst], achroa. — Differt ab aliis <em>Microcoleis </em>vagina distinctissirne undulato-constricta, transversim striata. Crassitudo fascicul. 0.010 millim., vaginae 0.016 millim ; diameter artic. 0.003 millim.','Schaarchmidt 1886',NULL,0,0),(1647,2083,'description','Trichomala obscure aeruginea, sparsa aut agglomerata, elongata, recta, flexilia, ad genicula leviler constricta, 2,5 um ad 5 um crassa, apice longe attenuata capitata uncinata vel undulata; articuli subquadrati, 2,5 um ad 4.2 um longi, apicalibus longioribus; dissepimenta lineis geminis tenue granulatis notata; cellula apicalis calyptram depresso-conicam praebens.','Gomont 1892',NULL,0,0),(1648,2084,'description','Forming a thin gelatinous membrane on dripping rocks, amorphous; sheaths of the trichomes at first thin, then more gelatinous and thicker, cohering. Internal trichomes aeruginous, slender, simple. Sheath variable with age. First barely discernible, then twice the diameter of the trichomes. Most frequently only one in a sheath, but sometimes two or three. Diameter, without sheath, 10-13 um.','Wolle 1887',NULL,0,0),(1649,2085,'description','Filaments tortuous, mostly open at the apices with extruding trichomes, smaller, younger ones closed; 30-60 trichomes densely entwined in the center of the filaments, 4.6-5 um diam., very bright blue-green in color: 2-3 cells attenuated at the apices, not constricted at the dissepiments; cells quadrate to twice as long as broad, densely congested with fine irregular granules; cross-walls very distinct; apical cell conical; sheath white, smooth, homogeneous, ample, 9-12 um<sup>​</sup> thick','Gardner 1927',NULL,0,0),(1650,2087,'description','Filaments solitary, rarely pseudobranched, to 50 μm wide; sheaths thick, firm, cylindrical, with crosswise lamellation in young stages; trichomes blue-green, many in a sheath, ± parallelly-arranged and coiled together, not constricted, 4-6 μm wide; cells ± quadratic.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1651,2090,'description','Filis stratum definitum non formantibus, sed numerosis ad superficiem stratuum Phormidii afiixis vel repentibus, flexuosis, fragilibus; vaginis achrois firmis tenuibus; trichomatibus inter cellulas haud constrictis, cellulis tam longis quam latis vel paulo brevioribus, cytoplasmate homogeneo dilute aerugineo, dissepimentis pellucidis, valde indistinctis; apice trichomatis plus minusve distincte attenuato, plerumque rotundato, interdum paulo capitato, saepe modiee arcuato. Diam. fil. = 5-6 um; diam. trich. = 4.8-5.7 um.','Fritsch 1912',NULL,0,0),(1652,2092,'description','Stratum expansum, fragile, nitens, atro-aerugineum, interdum luleo-fuscum. Fila recta, rarius flexuosa, varie in-tricata. Vaginae arctae, fragiles, mucosae, distinctae aut in mucum amorphum diffluentes at agglutinatae, chlorozincico iodurato non caerulescentes. Trichomata aeruginea, ad genicula haud constricta, 4 um ad 7 um crassa, apice breviter attenuata et eximie capilata vix curvata aut recta; articuli quadrati vel diametro ad duplo breviores, 2 um ad 5 um longi. Dissepimenla frequenter granulata; cellula apicalis calyptram rotundatam praebens.','Gomont 1892',NULL,0,0),(1653,2093,'description','Filaments solitary or in tufts; sheaths colourless or yellow, 20-40(-75) μm wide, with 8-25 or more trichomes; trichomes pale green, (3)3.2-3.5(4.2) μm wide, not constricted, attenuated at the ends; cells 3-7 μm long; apical cells rounded-conical or acute-conical.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1654,2094,'description','Stratum calce incruslatum, canescens, superficie aerugineum. Trichomata dilutissime aeruginosa, per totam longitudinem plus minusve laxe et regulariler spiralia aut interdum subrecta, fragilia, ad genicula haud constricta, 4 um ad 5 um crassa, apice evidenter attenuato eximie capitata; articuli quadrati vel diametro longiores, 4 um ad 7 um longi; dissepimenta lineis geminis grosse granulatis punctata; cellula apicalis calyptram conicam valde conspicuam praebens.','Gomont 1892',NULL,0,1),(1655,2095,'description','Stratum calce incruslatum, canescens, superficie aerugineum. Trichomata dilutissime aeruginosa, per totam longitudinem plus minusve laxe et regulariler spiralia aut interdum subrecta, fragilia, ad genicula haud constricta, 4 um ad 5 um crassa, apice evidenter attenuato eximie capitata; articuli quadrati vel diametro longiores, 4 um ad 7 um longi; dissepimenta lineis geminis grosse granulatis punctata; cellula apicalis calyptram conicam valde conspicuam praebens.','Gomont 1892',NULL,0,0),(1656,2096,'description','Ph. rivulare, compactum, coriaceum, lamellosum, atro-chalybeum; trichomatibus inaequalibus (diam. 1/700 - 1/350\'\')\' articulis in majoribus diametro duplo brevioribus, in minoribus diametro aeqnalibus; geniculis lineis gemiuls, transversalibus , punctatis notatis.','Kützing 1843',NULL,0,0),(1657,2099,'description','Filaments simple; sheaths thin, containing about 10 trichomes; trichomes blue-green, 4.5-5.7 μm wide, constricted at cross-walls; cells 7-14.3 μm long, apical cells conical.','Borge 1925',NULL,0,0),(1658,2100,'description','Lager büschelig-rasig, stahlblau bis schwärzlichviolett gefärbt, einzelne Büschel bis 5 mm lang. Fäden leicht gekrümmt, zu zwei bis 8 oder einzeln in farblosen, eng anliegenden Scheiden eingeschlossen. Veget. Zellen 9 bis 11 um dick, 1/3-1/2 mal so lang, mit stahlblauem oder röthlichbräunlichem Inhalte;','Hansgirg 1892',NULL,0,0),(1659,2103,'description','Stralum tenue, membranaceum, obscure viride. Trichomata vaginis carentia, muco amorpho paralleliter agglutinata, obscure aeruginosa, subrecta, non torulosa, 6 um ad 8um· crassa, apice recta vix attenuata et levissime capitata; articuli subquadrati vel diametro usque ad duplo breviores, 3 um ad 8 um longi; dessepimenta non granulata; cellula apicalis calyptram oblique depresso-conicam paebens.<sup>​</sup>','Gomont 1892',NULL,0,0),(1660,2104,'description','Stratum pannosum expansum rubro-fuscum, filis longis gracilibus intertextis copiose ramosis, basin usque ad 30 trichomata includentibus; vaginis hyalinis crassis gelatinosis inconspicue lamellosis vel fibrosis, ambitu erosis vel levibus vel diffluentibus, chlorozincico iodurato ad apices aegre caerulescentibus; trichomatibus laete aerugineis, 3 um ad 4 um crassis, ad genicula constrictis; cellulis diametro usque ad 2 1/2plo longioribus, protoplasmate non aut sparsim grosse-granuloso, dissepimentis conspicuis; cellula apicali acute conica.','Drouet 1943',NULL,0,0),(1661,2105,'description','Strato minutissimo, aliis algis adfixo; filamentis rectis leniterve incurvis, 2-4 (raro 1 vel pluribus) intra vaginam gelatinosam communem, tenuissimam, hyalinam fasciculatim consociatis, fasciculis saepe Schizotrichis more ramosis; filamentis singulis vagina propria tenui, arcta, hyalina donatis, circiter 2-2,5 um. latis, distincte articulatis; cellulis 3/4-1 longis quam latis, contentu dilute caeruleo-viridi, non vel vix granulato.','Hansgirg ex Forti 1907',NULL,0,0),(1662,2109,'description','Filamentis simplicibus longis, 6-30 um latis, trichomatibus 1-8 intra vaginam homogeneam hyalinam consociatis, vagina extrinsecus corpusculis alienis adhaeris ornata; cellulis 2,5-3 um latis 5-7 um longis; contentu homogeneo, ad septum nom constrictis, apicalibus in aciculam terminatis.','González Guerrero 1946',NULL,0,0),(1663,2110,'description','Fila stratum sordide vel nigro virescens, panuosum, longe lateque expansum, compactum, stratificatum, stratis discoloribus, formantia, aut sparsim inter varias Algas crescentia, tortuosa, haud saepe ramosa. Vaginae cylindraceae, ambitu plus minusve inrequales et erosae, apice plerumque apertae, interdum omnino diffluentes chlorozincico iodurato non caerulescentes. Trichomata Iaete aeruginosa, brevia, subrecta, intra vaginam, in fasciculos vulgo apice acuminatos, raro funiformi-contortes, arctissime aggregata, ad genicula conslricla, 2,5 um ad 6 um crassa; articuli subquadrati, aut ad &nbsp;duplo longiores quam latiores, 3,6 um ad 10 um Iongi; dissepimenta non granulata; cellula apicalis haud capitata, acute conica.','Thuret ex Gomont 1892',NULL,0,0),(1664,2110,'description','Fila stratum sordide vel nigro virescens, panuosum, longe lateque expansum, compactum, stratificatum, stratis discoloribus, formantia, aut sparsim inter varias Algas crescentia, tortuosa, haud saepe ramosa. Vaginae cylindraceae, ambitu plus minusve inrequales et erosae, apice plerumque apertae, interdum omnino diffluentes chlorozincico iodurato non caerulescentes. Trichomata Iaete aeruginosa, brevia, subrecta, intra vaginam, in fasciculos vulgo apice acuminatos, raro funiformi-contortes, arctissime aggregata, ad genicula conslricla, 2,5 um ad 6 um crassa; articuli subquadrati, aut ad &nbsp;duplo longiores quam latiores, 3,6 um ad 10 um Iongi; dissepimenta non granulata; cellula apicalis haud capitata, acute conica.','Thuret ex Gomont 1892',NULL,0,1),(1665,2111,'description','Filaments solitary, nearly straight or ± undulate, long, up to 40 μm wide. Sheaths variably thick, ± uneven at the margins, open at the ends, usually partly or totally diffluent, containing 4-8 trichomes parallelly-arranged or rope-like contorted. Trichomes reddish or pale blue-green (when dried), about 4 μm wide, seemingly long; nearly straight or undulated, not constricted at the cross-walls. Cells nearly isodiametric or 1/2 as long as wide, 2-4 μm long; cell content fine granulated, frequently covering the cross-walls. Apical cells obtuse-conical, without calyptra or thickened cell wall.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1666,267,'description','Stratum nigro- vel fusco-aeruginosum, valde expansum, membranaceum, coriaceurn. Fila elongata, plus minusve flexuosa, arcte intricala. Vaginae tenues, papyraceae, aut in mucum amorphum diffluentes, chlorozincico iodurato caerulescentes. Trichomata aeruginosa, ad genicula non constricta, apice recta breviter attenuata non capitata, 3 um ad 4.5 um crassa; articuli subquadrati vel diametro ad duplo longiores, 3.4 um ad 8 um longi, granulis protoplasmaticis haud frequenter farcti; dissepimenta non granulata, vulgo conspicua; cellula apicalis obtuse conica; calyptra nulla','Gomont ex Gomont 1892',NULL,0,0),(1667,2112,'description','Stratum nigro- vel fusco-aeruginosum, valde expansum, membranaceum, coriaceum. Fila elongata, plus minusve flexuosa, arcte intricala. Vaginae tenues, papyraceae, aut in mucum amorphum diffluentes, chlorozincico iodurato caerulescentes. Trichomata aeruginosa, ad genicula non constricta, apice recta breviter attenuata non capitata, 3 um &nbsp;ad 4.5 um crass ; articuli subquadrati vel diametro ad duplo longiores, 3.4 um ad 8um longi, granulis protoplasmaticis haud frequenter farcti; dissepimenta non granulata, vulgo conspicua; cellula apicalis obtuse conica; calyptra nulla.','Gomont ex Gomont 1892',NULL,0,0),(1668,2115,'diagnosis','Filis stratum aerugineum praebentibus, circ. 36 um crassis, simplicibus, trichomatibus permultis subparallelis, rectis aut funis instar contortis, in vagina communi hyalina chlorozincico iodurato non caerulescente arete aggregatis, confectis. Trichomatibus simplicibus, vagina propria tenuissima cinctis, elongatis, circ. 4 um crassis, ad genicula non constrictis, extra vaginam communem directis, apicibus leniter attenuatis, haud capitatis. Cellulis diametro trichomatis aeque fere longis, aut interdum etiam duplo longioribus aut brevioribus, compagibus haud granulatis; cellula apicali paene semiglobosa.','Carlson 1913',NULL,0,0),(1669,2115,'description','Thallus blue-green; filaments unbranched, containing many trichomes; sheaths colourless; trichomes about 4 μm wide, cells longer than wide or shorter; apical cells nearly hemispherical.','Komárek &amp; Anagnostids2005',NULL,0,0),(1670,2116,'description','Lager compact, hautartig, geschichtet, braun, olivengelb oder dunkel blaugrün, unten entfärbt. Fäden gekrümmt, dicht verflochten, ohne Scheiden 8 bis 14, mit diesen 12 bis 22 um dick. Veget. Zellen 1/6 bis 1/3 mal so lang als breit, mit blaugrünem oder bräunlichem Inhalte. Scheiden dünn, seltener bis 4 um dick, farblos oder gelb bis braungelb, bei der auf feuchter Erde vegetirenden Form öfters an der Oberfläche rauh.','Hansgirg 1892',NULL,0,0),(1671,2116,'description','Thallus toughy, layered, filaments coiled 12-22 μm, trichomes 8-14 μm wide; sheaths thick.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1672,2117,'diagnosis','Fila variis algis consociatis, simplicia; vaginae mucosae, achroae, apice evanescentes. Trichomata subparallela subtortiave intra vaginam permulta; articulis diametro paullo longioribus; dissepimenta distincta non granulata, cellula apicalis obtusa. Crass, trich. 1.5 -2.0 um; diam. vag. circ. 45 um .','West et West 1896',NULL,0,0),(1673,2118,'description','Filaments branched, cylindrical, articulate, bluish-green, branches inclosed in bundless within a sheath, joints very short.','Harvey 1841',NULL,0,0),(1674,2076,'diagnosis','Thallus filamentosus, prostratus, caeruleus, 30.8-47.2 um diametro; filamenta funiformia, infra torta, ad apices ramosa; vaginae firmae, incolores vel flavidae, parum lamellosae; trichomata in vagina pluria vel 1-2, ad genicula manifeste constricta, ad apices attenuata; cellulae apicales rotundato-conicae, vel acuto-conicae; cellulae subquadratae vel usque 2plo lariores quam longiores; protoplasma caeruleum, haud granulatum. Cellulae 6.2-8.1 x 3.5-6.7 um.','Azevedo 1991',NULL,0,0),(1675,2076,'description','Thallus filamentous, creeping, blue-green, 30.8-47.2 um in diameter; filament rope-like, twisted in the lower part, branched at the apices; shaeths firm, colourless or yellowish, slightly lamellose; trichomes several or 1-2 in a sheath, clearly constricted at the cross walls, apices sometimes tapered; apical cells rounded-conical, rounded or acute-conical; cells squarish to 2 times broader than long, cell content blue-green, homogeneous. Cells 6.2-8.1 x 3.5-6.7 um.','Azevedo 1991',NULL,0,0),(1676,2075,'description','Thallus filamentous, creeping, prostrate, blue-green; filaments to 47.2 μm wide, pseudobranched at the apices; sheaths firm, colourless or yellowish, slightly lamellose, containing 1-2 trichomes (acc. to drawing up to 5-6), open at the ends; trichomes constricted, blue-green, cells ± &nbsp;quadratic to 2x shorter than wide.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1677,2077,'diagnosis','Thallus constans ex tege tenui plana, aeruginosus. Fila vagina carentibus in culturis, 6 um lata. Trichomata motu prolapso, ad septa non constricta, divisione cellularum ut in Oscillatoriaceis, necridiis carentibus, non decresentia vel leviter decrescentia in cellulis apicalibus 2–4, 6 um lata pro parte majore, ad apices ad 4.5 um decrescentia. Cellulae aeruginosae, granulis minutis in centroplasmate, cum vel sine granulis ad septa, chromoplasmate peripheralibus per microscopium lucens visibilibus, thylakoidibus peripheralibus fasciculatis per microscopium electronicum visibilibus, 3– 6 um longae inter septa completa. Cellulae apicales obtusiconicae, breviores quam latiores, calyptra non capitata.','Casamatta &amp; Johansen in Casamatta et al. 2005',NULL,0,0),(1678,2077,'description','Thallus thin flat mat of filaments, blue-green. Filaments in culture without evident sheath, 6 um wide. Trichomes with gliding motility, unconstricted at the crosswalls, with cell wall formation commencing before prior cell division is complete as in the Oscillatoriaceae, without necridia, not or slightly tapering in the last 2–4 apical cells, 6 um wide in the majority of the trichome, tapering as narrow as 4.5 um at the apices. Cells bluegreen, with minute granules in the centroplasm, with or without granules at the crosswalls, with marginal chromoplasm visible in light microscope, with peripheral fascicular thylakoids visible by means of the electron microscope, 4–6 um long between complete cell walls. End cells bluntly conical, shorter than wide, with a noncapitate calyptra.','Casamatta et Johansen in Casamatta et al. 2005',NULL,0,0),(1679,2077,'etymology','Named for Judy Acreman, who isolated this strain, maintains the UTCC collection, and was helpful throughout this study.','Casamatta et Johansen in Casamatta et al. 2005',NULL,0,0),(1680,2088,'other','Thallus constans ex tege effusa filorum visibilium, olivaceus. Fila trichomatibus singularibus, non pseudoramosa, 7– 9 um lata. Vagina incolorata, tenuis, non lamellata, aperta, sed raro ultra apicem trichomatis extensa. Trichomata recta vel flexuosa, ad septa non constricta, necridiis carentibus, ad apicem decrescentia, 6–7 um lata. Cellulae granulares, grulis prope septa apprime aggregatis, septis vix visibilibus, thylakoidibus peripheralibus fasciculatis per microscopium electronicum visibilibus, breviores quam latiores, 1.5–3.5-(5) um longae. Cellulae apicales obtusirotundatae ad obtusiconicae, infrequenter calyptratae, sed nunquam capitatae in aspecto.','Casamatta et Johansen in Casamatta et al. 2005',NULL,0,0),(1681,2088,'description','Thallus a spreading mat of filaments that are visible to the naked eye, olive-green in color. Filaments with one trichome only, without false branching, 7–9 um wide. Sheath colorless, thin, unlamellated, open, but rarely extending past the trichome apex. Trichomes straight or flexuous, not constricted at the crosswalls, lacking necridia, tapering toward the apex, 6–7 um wide. Cells granular, with granules especially concentrated at the crosswalls, with peripheral fascicular thylakoids visible &nbsp;by means of the electron microscope, with cross walls scarcely visible, shorter than broad, 1.5–3.5–(5) um long. End cells bluntly rounded to bluntly conical, &nbsp;infrequently calyptrate, but never capitate in appearance.','Casamatta et Johansen in Casamatta et al. 2005',NULL,0,0),(1682,2088,'etymology','Named for its region of origin','Casamatta et Johansen in Casamatta et al. 2005',NULL,0,0),(1683,2098,'description','Filis 1/1500 lin. crassis, aerugineis v. lutescentibus, indistincte articulatis, parum flexuosis, &nbsp;aplce attenuatis, in fasciculos pullide fuscos, 1/300 lin crassos, flexuosos, contortis; vaginis ad 1/100 lin. crassis, pellucidis, fibrillosis, margine undulatis.','Zeller 1873, Hedwigia 12: 169-170',NULL,0,0),(1684,2107,'diagnosis','Trichomatibus calce non incrustatis, per totam longitudinem plus minusve laxe et regulariter spiralibus, rarius rectis, ad genicula haud longitudinem, 4-5.5 um lat., ad apices evidenter attenuatis, rectis vel interdum uncinatis, eximie capitatis. Articulis quadratis vel diametro longioribus, 4-7 um long.; dissepimentis lineis geminis grosse granulatis punctatis. Cellulis apicalibus calyptram conicam valde conspicuam praebentibus.','Elenkin et Kosinskaja in Elenkin 1949',NULL,0,0),(1685,2119,'diagnosis','Filaments simplicibus vel in fasciculis parvis, flexuosis stratis <em>Schizothricis friesii</em> /Ag.) Gom. affixis, vaginis achromis, non stratosis apice apertis at omnino diffluentibus, chlorozincico iodurato non coerulescentibus; trichomatibus pulchre aerugineis, intra vaginam 1-30, plerumque funiformi-contortis, ad dissepimenta leviter constrictis; cellulis cylindricis, diametro circiter duplo longioribus, contentu tenuissime granulato, dissepimentis non granulosis; cellulis apicalibus rotundatis vel plus minusve obtuse conicis. Latitudo filamentorum usque ad 30 um; latitudo cellularum (vel trichomatum) 2.0-2.5 um, saepissime 2.2-2.3 um; longitudo cellularum 3.5-6.0 um; longitudo cellularum apicalium usque ad 7.7 um.','Starmach 1960',NULL,0,0),(1686,2123,'description','Stratum nigro-aerugineum, siccitate atro-chalybeum, modice expansum papyraceum, aut crassum basi affixum fluitans. Trichomata plerumque vagin a carentia, muco amorpho, chlorozincico iodurato non caerulescente agglutinata, aeruginea, elongata, plus minusve flexuosa, non torulosa, 4,5 um ad 9 um crassa, extremitatem versus recta aut laxissime spiralia; apice sensim attenuata, eximie capitata; articuli quadrati vel diamelro ad duplo breviores, 3 um ad 7 um longi; dissepimenta lineis geminis margaritaceo-punctatis notata; cellula apicalis obtuse truncata, calyptram subhaemisphericam praebens.','Gomont 1892',NULL,0,0),(1687,2123,'description','Thallus black, blue-green or olive-green, occasionally slightly incrusted with CaCO<sub>3</sub>, dark steel-blue when dried, forming expanded papyraceous or thickly attached layers to submerged substrates. Filaments long, ± curved or straight, sometimes regularly loosely spirally-coiled or only at the ends. Sheaths usually absent, or fine, thin, diffluent, mucilaginous. Trichomes blue-green, (4)4.5-7.5(9) μm wide, not constricted at the coarsely granulated cross-walls, slightly gradually attenuated at the ends and capitate. Cells isodiametric to 1/2x as long as wide, rarely slightly longer, (2.4)3-7 μm long; cell content homogeneous. Apical cells capitate, with obtuse-conical to nearly hemispherical calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1688,2123,'eco_distro','Freshwater, mostly in cold, flowing freshwaters on limestone substrates (in rivers, cataracts), benthic attached on rocks, stones, on sand, and hydrophytes; data from thermal springs should be revised. Records also exist about this species boring into limestone, or participating in the formation of \'Furchensteine\' at the littoral of lakes (the taxonomic identity must be confirmed); distributed worldwide, possibly cosmopolitan.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1689,2127,'description','Filaments very slender.','Hassall 1845',NULL,0,0),(1690,2129,'description','Caespites molles, sordide virescentes aut obscure aruginei, ad tria centimetra alti. Fila subdichotome aut fasciculatoramosa. Vaginae hyalinae vel sordide luteo-virescentes, &nbsp;crassae, agglutinantes, transverse repetite corrugatae et quasi squamosae, non diffluentes, apice clausae et acuminatae aut apertae. Trichomata aeruginosa, intra vaginam ad basim filorum pauca, superne permulta, subrecta, parallela, haud funiformi-contorta, ad genicula constricta, 4 um ad 5,5 um crassa; articuli subquadrati vel diametro trichomatis ad triplo longiores, 3,5 um ad 12 um. longi, interdum protoplasmate grosse granuloso farcti; dissepimenta haud granulata; cellula apicalis acute conic.','Kützing 1849 ex Gomont 1892',NULL,0,0),(1691,2134,'description','Filamenta per algas alias sparsa, non stratum formantia; vaginis firmis, hyalinis, comparate levibus, trichomata usque ad 25 arcte collecta includentibus; trichomatibus aeruginosis, 6-6.5 um diam., ad apices lente attenuatis, neque capitatis neque constrictis; cellulis 2-3 um longis, protoplastis homogeneis.','Setchellet Gardner 1937',NULL,0,0),(1692,2135,'description','Lager blaugrün, dünn, krustenartig, oft weit ausgebreitet, häufig auch einzelne Bündel unter andern Algen; Fäden sehr dünn, wenige in einem Bündel; Zellen ungefähr so lang wie dick, an den Scheidewänden eingeschnürt, mit hell bläulichem Inhalt; gemeinsame Scheiden weit, ungeschichtet, farblos, an den Enden getheilt. Fäden 1,1-1,5 um, Scheiden - 7,5 um dick.','Kirchner 1878',NULL,0,0),(1693,2136,'description','Thallus blackish to dark blue-green, or greyish. Sheaths lacking or rarely developed. Trichomes purple-greyish or bluish (when dried!), straight, flexible, 6-11.2 μm wide, not constricted at the sometimes granulated cross-walls, not attenuated at the ends. Cells 1-1/2x as long as wide, 4-11 μm long. Apical cells convex, slightly capitate, with thickened cell walls.','Komárek &nbsp;&amp; Anagnostidis 2005',NULL,0,0),(1694,2136,'eco_distro','Freshwater, in stagnant and flowing waters, also on moist rocks, not very common; Europe: France, Germany, Poland, Scotland, Sweden, Switzerland; outside Europe: Afghanistan, Africa (Gabon), Australia, Azores, Japan, islands in Indian Ocean, etc.','Komárek &nbsp;&amp; &nbsp;Anagnostidis 2005',NULL,0,0),(1695,2137,'description','Stratum nigro-chalybeum. Trichomata livide purpureochalybea (sec. Kützing), in speciminibus siccis hyalina vel pallide caerulea, recta, flexilia, non torulosa, 6 um ad 11 um crassa, apice haud attenuata subcapitata admodum recta; articuli quadrati vel diametro ad duplo breviores, 4 lum ad 11 um longi; protoplasma in speciminibus siccis pellucidum, vix granulosum; dissepimenta passim granulis protoplasmaticis crassis notata; membrana cellulae apicalis superne convexa, evidenter incrassata.','Kützing ex Gomont 1892',NULL,0,0),(1696,2138,'description','Filaments in fascicles, later forming mucilaginous mats; sheaths wide, gelatinous, colourless, not lamellated, constricted, containing one to several to many trichomes; trichomes 5.8-7.3 μm wide, cells ± isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1697,2138,'eco_distro','Freshwater; on shores (on mosses or shells of<em>&nbsp;Dreissenia</em>) of &nbsp;Lake Ochrid, Montenegro.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1698,2097,'diagnosis','Fila in stratum nigro-aerugineum intricata., tortuosa, simplicia aut vage ramosa et apice bifida. Vaginae subtenues, mucosae et agglutinantes, interdum diffluentes, apice saepius evanescentes, chlorozincico iodurato hand caerulescentes. Trichomata laete aeruginosa, subparallela, extra vaginam rectissima, ad genicula eximie constricta, 4 um ad 5 um crassa, articuli passim subdoliiformes, diametro trichomatis paulum vel ad triplo longiores, 6 um ad 12 um longi, granulis protoplasmaticis globulosis sparsim farcti; dissepimenta haud granulata; cellula apicalis plus minusve obtuse conica, haud capitata.','Farlow ex Gomont 1892',NULL,0,0),(1699,2140,'description','Lager blaugrün, dünn, krustenartig, oft weit ausgebreitet, häufig auch einzelne Bündel unter andern Algen; Fäden sehr dünn, wenige in einem Bündel; Zellen ungefähr so lang wie dick, an den Scheidewänden eingeschnürt, mit hell bläulichem Inhalt; gemeinsame Scheiden weit, ungeschichtet, farblos, an den Enden getheilt. Fäden 1,1-1,5 um, Scheiden - 7,5 um dick.','Kützing ex Kirchner 1878',NULL,0,0),(1700,2141,'description','Die Alge bildet 4-5 und mehr Millimeter lange, schmale, im ganzen ca. 60 um breite, nach vornen sich verschmälernde und nicht zerteilte Büschel, welche an Wasserpflanzen angewachsen sind. Die Scheide ist sehr breit, gelatinös, mit un regelmässigem, zerfliessendem Rande. Sie enthält an der Basis ca. 6-18 dicht aneinander gelagerte und meist nicht gerade verlaufende Fäden, deren Zahl nach aufwärts abnimmt. Die Zellen sind 3-4 um breit und um das doppelte länger (6 —10 um), rechteckig, blaugrün, in Längsreihen sehr fein granuliert und im Spiritus materiale meist nur lose zusammenhängend. Die Endzellen sind nicht verschmälert und breit abgerundet.','Schmidle 1897',NULL,0,0),(1701,2141,'description','Filaments 4-5 mm long, unbranched, sheaths thick, diffluent, containing 6-18 trichomes; trichomes blue-green, 3-4 μm wide, not constricted at cross- walls; cells up to 2x longer than wide; apical cells widely-rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1702,2144,'description','Ph. limicola, late expansum , viridi-nigrum; trichomatibus in radios aerugineos, raro fuscescentes prorepentibus, inaequalibus (diam.1/1200´´-1/450\'\'); articulis diametro aequalibus, vel (ut in tenuioribus) triplo longioribus, hyalinis; apiculo attenuato, obtuso.','Kützing 1843',NULL,0,0),(1703,2145,'diagnosis','Stratum firmum, crassiusculum, superficie atro-viride, subtus plus minusve decoloratum. Fila modice flexuosa, subparallela. Vaginae in mucum fibrosum diffluentes, chlorozincico iodurato non caerulescentes. Trichomata olivacea, ad genicula !eviter constricta, 7 um ad 8 um crassa, apice recta et plus minusve attenuato-capitata, passim quasi mucronata; articuli brevissimi, diametro trichomatis duplo ad quadruplo breviores, 2 um ad 2,5 um longi; dissepimenta lineis binis punclatis granulata; cellula apicalis superne rotundata aut subconica, calyptram praebens.','Kützing ex Gomont 1892',NULL,0,0),(1704,2146,'other','Ph. riparium, expansum, viridi-atrum non lamellosum; trichomatibus aequalibus (diam. 1/690\'\'); omnibus vaginatis, flexuosis, parallelis, virescentibus; articulis confluentibus, non granulosis; vaginis coalitis, arctissimis, hiyalinis, laevissimis.','Kützing 1843 as Ph. lyngbyaceum',NULL,0,0),(1705,2153,'diagnosis','Filis pulchre aerugineis, 5-6 um crassis, ad 200 um longis; vaginis omnino diffluentïbus; trichomatïbus 3-8 arcte funiformi-contortis, subtorulosis, 1,2-1,5 um crassis, apicem versus non attenuatis; articulis subquadratis, contentu homogeneo; cellula apicali extus hemisphaerica, haud capitata.','Frémy 1930',NULL,0,0),(1706,2154,'diagnosis','Filis inter alias algas lignicolas sparsis, ad 30 um crassis, passim pseudoramosis; vaginis modice mucosis, cylindraceis, tenuibus, apice evanescentibus, chlorozincico iodurato haud caerulescentibus; trichomatibus in eadem vagina saepe permultis, arcte congestis, subparallelis, rectis aut spiralïbus, laete aerugineis, ad genicula haud constrictis, 2 um crassis; articulis subquadratis aut diametro trichomatis 1,5-plo longioribus; dissepimentis aegre conspicuis<sup></sup>;<sup></sup> protoplasmate omnino homogeneo; cellula apicali acute conica, haud capitata.<sub>​</sub>','Frémy&nbsp; 1930',NULL,0,0),(1707,2154,'description','Filaments solitary, ± 30 μm wide, sometimes divaricated, with many trichomes, which are bright blue‑green, 2 μm wide, not constricted at cross‑walls, sheaths slightly mucilaginous, diffluent at the ends, cells ± isodiametric to 1.5x longer than wide, apical cells shortly-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1708,2154,'eco_distro','Subaerophytic, corticolous on moist bark of trees, tropical central Africa.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1709,2155,'diagnosis','Filis repentibus, in strato Calothricis Bossei intermixtis, redis aut undulatis, valde elongatis, ad 30 um crassis, raro pseudoramosis; vaginis cylindraceis, laevibus, tenuibus, apicem versus evanescentibus, interdum omnino diffluentïbus, chlorozincico iodurato haud caerulescentibus; trichomatibus violaceis intra vaginam permultis, arcte congestis, parallelis aut saepius funiformi-contortis, extra vaginam redis, ad genicula haud constrictis, apice nec attenuatis nec capitatis, 1,2-1,5 um crassis; articulis subquadratis vel diametro trichomatis ad duplo longioribus, 1,2-3 umi longis, contentu homogeneo; cellula apicali cylindrato-conica.','Frémy 1930',NULL,0,0),(1710,2155,'description','Filaments prostrate, very long, ± 30 μm wide, rarely divaricated with many trichomes, which are violet, 1.2‑1.5 μm wide, not constricted at cross‑walls; sheaths thin, sometimes entirely diffluent; cells ± isodiametric to 2x longer than wide, 1.2‑3 μm long, apical cells cylindrical and rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1711,2155,'eco_distro','Freshwater, submerged in springs on quarzite rocks and &nbsp;benthic on siliceous stones, &nbsp;from 2‑5m of depth, tropical Africa (Gabon).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1712,2156,'diagnosis','Fila inter varias Algas crescentia, aut in stratum nigro-aeuginosum intricata, tortuosa, simplicia aut apice bifida. Vaginae modice mucosae, apice evanescentes et apertae aut acuminatae et clausa, chlorozincico ioddurato non caerulescentes. Trichomata laete aeruginosa, parallela, recta, aut funilformi-contorta, ad genicula non constricta 5um ad 7 um crassa; articuli diametro trichomatis circiter vel eo ad duplo longiores, 4 um ad 13 um longi; haud granulala; cellula apicalis haud capitata.','Gomont 1892',NULL,0,0),(1713,2156,'description','Filaments solitary or forming a dark blue-green thallus, unbranched or sometimes divided at the ends, to 50 μm wide and to 1600 μm long. Sheaths slightly mucilaginous, open and diffluent at the ends or closed and pointed, colourless, containing usually many straight, parallelly-arranged or rope-like twisted trichomes. Trichomes bright blue-green, 4.6-7 μm wide, not constricted at the not or granulated cross-walls, not attenuated at the ends. Cells nearly isodiametric or up to 2x longer than wide, 4-13(14) μm long. Apical cells not capitate, conical, sometimes acute-conical and slightly bent.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1714,2156,'eco_distro','Freshwater, in stagnant waters, on wet rocks and soils, at lake margins, widely distributed in the north temperate zone (Europe, USA); recorded also from moist soils in N Africa','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1715,2158,'diagnosis','Trichomatibus inaequalibus, pulchre aerugineis vel smaragdinis, rarius e luteolo viridibus, indistincte articulatis, in fasciculos flexuosos anastomosantes intricatos contortis, 2-4,5 um crassis; articulis diametro aequalibus vel duplo triplove longioribus vaginis crassis, gelatinoso-diaphanis, lamelloso-fibrillosis, apice<br>clausis vel apertis contentu granuloso.','Forti 1907',NULL,0,0),(1716,2158,'description','Filaments consisting of contorted fascicles of trichomes; sheaths colourless, lamellated; trichomes blue-green or yellowish-green, 2-4.5 μm wide; cells shorter than wide to isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1717,2160,'description','Lager hautartige, gelbbraune, meist dünne, etwas schlüpferige Ůberzüge auf am Ufer des Meeres an der Fluthgrenze untergetauchten Felsen, Steinen, Muscheln etc. bildend. Fäden meist zu 2 bis 6, seltener mehre oder blos einzeln, in einer gemeinsamen, geschichteten, ziemlich dicken Scheide eingeschlossen, aus welcher sie blos an den Enden hervorragen, wobei dann an jedem Faden noch die eng anliegende, farblose, dünne Specialscheide sichtbar wird. Die Zellen der Faden etwa 1/2 bis 1 um breit, 1 bis 2 mal so lang, mit blass blaugrünem, seltener olivengelblichem gekorntem Inhalte. Gemeinsame Gallertscheiden mit 6 Fäden, an der Basis etwa 6 bis 10 um breit, mit gelben bis &nbsp;goldgelben innern imd fast farblosen äusseren Schichten, meist wie<br>derholt fast dichotomisch getheilt.','Hansgirg 1890',NULL,0,0),(1718,2159,'description','Thallus membranaceous, yellow‑brown, mostly thin, slightly mucilaginous. Filaments repeatedly subdichotomously divaricated, ± 6‑10 μm wide. Sheaths thick, lamellated, inside gold‑yellow to brownish, outside nearly colourless, containing solitary, or rather 2‑6, rarely more trichomes. Trichomes pale blue‑green or yellowish green, 0.5‑1 μm wide, with narrow, special sheaths. Cells up to 2x longer than wide. Apical cells rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1719,2159,'eco_distro','Marine, on stones, mussel valves and algae, described from Adriatic Sea (Istria, Dalmatia).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1720,2133,'description','Lager endophytisch, im Thallus verschiedener marinen oder im Brack- und im Sůsswasser lebenden Rivulariaceen (insb. der marinen <em>Rivularia atra)</em>, seltener auch im Gallertlager einiger Lyngbyaceen. Faden zu 2 bis 8 bis 16, seltener einzeln, oder mehrere bündelweise vereinigt, in einer gemeinsamen, enganliegenden, farblosen, dünnen Gallertscheide, mit der Specialscheide 0.7 bis 1 seltener bis 1.5 um dick, oft undeutlich gegliedert, am Ende öfters verdünnt, resp. mit einem schnabelartigen Fortsatze der dünnen, farblosen Specialgallertscheide versehen. Veget. Zellen 1 bis 21/2 mal so lang als breit, mit oft sehr blass bläulichgrünem, feingekörntem Inhalte. Einzelne Bündel von 6 und mehr Fäden sind 6 bis 10 um dick.&nbsp;','Hansgirg 1890',NULL,0,0),(1721,2161,'description','Stratum molle, expansum, aerugineum aut fuscum, lapides et plantas aquaticas investiens, usque ad 5 cm altum, filis elongatis, substrictis aut subflexuosis, penicillatim aggregatis, fasciculatim pseudo-ramosis pseudo-ramis subadpressis, inferne subsimplicibus; vaginis hyalinis demum luteolis, non aut modice lamellosis, chlorozincico iodurato pulchre caerulescentibus, ambitu irregularibus aut erosis, frequenter (in speciminibus siccis) transverse plicatis, crassis vel in statu juvenili tenuibus cylindraceisque; trichomatibus aerugineis, ad genicula non aut leviter constrictis, 4 um ad 6 um crassis, plerumque intra vaginam singulis binisve aut ad bases filorum usque ad quinqueis, apice non aut leviter attenuata; articulis diametro trichomatis longioribus, raro subquadratis, 3.5 um ad 10 um longis; protoplasmate dense grosse-granuloso, dissepimentis haud granulatis; cellula apicali rotundata vel obtuse conica.','Drouet 1939',NULL,0,0),(1722,2161,'description','Thallus expanded, blue-green or brownish, to 5 cm thick. Filaments fasciculated, sheaths hyaline or yellowish, slightly lamellate, thick; trichomes blue-green, 4-6 μm wide, not or slightly constricted, cells 5-7 μm long.&nbsp;','Komárek &amp; Anagnostidis 2005&nbsp;',NULL,0,0),(1723,2161,'eco_distro','Aquatic, on stones and submerged plants; known from eastern USA.','Komárek &amp; Anagnostidis 2005&nbsp;',NULL,0,0),(1724,2162,'description','Filaments 15-25 um (up to 50 um) thick, acuminate, scattered promiscuously among other algae, more or less contorted, closed at the apices when young, dissolving, and the trichomes protruding at the apices when older, with the trichomes crowded close to each other in the center and more or less intertwined but finally separating into separate strands and forming new filaments; trichomes up to 60 or more within a sheath, mostly parallel, 1.7-1.9 um diam., pale purplish-drab, not constricted, with acute and in part uncinate apices; cells homogeneous, 3-4 times as long as the diam.; sheath hyaline, homogeneous, somewhat gelatinous and irregular along the margin.','Gardner 1927',NULL,0,0),(1725,2163,'diagnosis','Filis cinereo-hyalinis rigidiusculis in fasciculum filiformem flexuosum elongatum nigrum subsimplicem apice penicillatum paralleliter &amp; densissime compactis.','Agardh 1824',NULL,0,0),(1726,2164,'description','Stratum pulchre arugineum, vel atro-chalybeum, crassum, compactum, aut rarius fasciculi penicillati, necnon arbusculiformes et vage ramosi, basi affixi, fluctuantes. Fila varie intricata, plus minusve recta, fragilia. Vaginae tenues, fragiles, plerumque in mucum amorphum prolinus diffluentes, chlorozincico iodurato non caerulescentes; trichomataaœruginea, ad genicula vulgo non constricta, rarius passim torulosa, apice recta. non capitata, 4,5 um· ad 12 um crassa; articuli diametro trichomatis breviores aut longiores, 4 um ad 9um longi, protoplasmate granuloso dissepimenta interdum obducente farcti; dissepimenta non granulata; cellula apicalis vix attenuata, truncata, membranam superne vix incrassatam praebens.','Gomont 1892',NULL,0,0),(1727,2165,'description','Lager haut- bis lederartig, compact, geschichtet, kurz strahlend, lebhaft blaugrün oder stahlblau bis schwärzlichgrün, die unteren Schichten meist entfärbt. Fäden gerade oder leicht gekrümmt, mit den leicht verschleimenden, dünnen Scheiden 6.8 bis &nbsp;8 um dick. Veget. Zellen fast so lang wie breit, an den Scheidewänden leicht eingeschnürt, mit blaugrünem Inhalte; Endzellen abgerundet, heller oder rosenroth gefärbt;','Hansgirg 1892',NULL,0,0),(1728,2165,'description','Thallus toughy, filaments 6.8-8 μm wide, cells blue-green, ± isodiametric.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1729,2165,'eco_distro','On wet rocks, central Europe.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1730,2166,'description','Filaments 9.6-16 mic. in diameter, forming a loose, cobwebby mass within sandstone rock, as far at least as 10-15 mm from surface; sheaths cylindrical, rough, usually colorless and not lamellose, but sometimes brownish and lamellose; trichomes 3.5-4.8 mic. in diameter, not constricted at the joints, one to many in a sheath; apical cell truncate conical; cells 5-8 mic. in length; transverse walls usually invisible.','Tilden 1910',NULL,0,0),(1731,2166,'eco_distro','In bare and dry sandstone cliffs. Soldiers\' Home, Minnehaha Falls. September 1896, Minnesota.','Tilden 1910',NULL,0,0),(1732,2167,'diagnosis','Thallus constans ex tege effusa ﬁlorum visibilium, aeruginosus ad brunneoviridis hebetatus. Fila trichomatibus singularibus, non pseudoramosa, 10–12 um lata. Vagina incolorata, ﬁrma, non lamellata, ultra apicem trichomatis extensa, 0.5–1.0 um crassa. Trichomata ad septa non constricta, divisione cellularum ut in Oscillatoriaceis, necridiis, 8–10 um lata. Cellulae aeruginosae, atroaeruginosae, vel atropurpureae, granulis minutis ad grandi in centroplasmate, thylakoidibus peripheralibus fasciculatis per microscopium lucens et microscopium electronicum visibilibus, 3–7 um longae. Cellulae apicales obtusiconicae ad obtusirotundatae.','Casamatta et al. 2005',NULL,0,0),(1733,2167,'description','Thallus a spreading mat of ﬁlaments visible to the naked eye, penetrating the agar, blue-green to a dirty brownish green. Filaments with a single trichome only, not false branched, 10–12 um wide. Sheath colorless, ﬁrm, unlamellated, extending past the trichome apex, 0.5–1.0 um thick. Trichomes unconstricted at the crosswalls, with cell wall formation commencing before prior cell division is complete as in the Oscillatoriaceae, with necridia, 8–10 um wide. Cells blue-green, blackish blue-green, or blackish purple, with minute to large granules in the centroplasm, with peripheral fascicular thylakoids visible in both light microscope and electron microscope, 3–7 um long. End cells bluntly conical to bluntly rounded.','Casamattaet al. 2005',NULL,0,0),(1734,2167,'etymology','Named for Samuel R. Rushforth, graduate advisor, mentor, collaborator, and friend','Casamatta et al. 2005',NULL,0,0),(1735,2169,'description','Filaments with diffluent, open sheaths; numerous trichomes constricted at cross-walls, (2)2.2‑2.5(2.7) μm wide, cells (2.5)4.5‑7.5(9) μm long; apical cells conical and sharply pointed, sometimes slightly curved.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1736,2169,'eco_distro','Among other algae on wet stones and walls, described from Portugal.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1737,2170,'description','Filaments solitary, straight or irregularly curved, mostly 12‑50 μm wide; sheaths colourless, sometimes diffluent; trichomes pale blue‑green, (0.6)0.8‑1 μm wide, constricted at cross‑walls; cells up to 4 μm long; apical cells rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1738,2170,'eco_distro','Marine, on rocks, among other cyanoprokaryotes in lagoons and in lower littoral belt, described from West Indies (St. Croix, Bonaire Island), known also from Argentina and Japan.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1739,2173,'diagnosis','Stratum tenue, arachnoideum, fusco-purpureum, siccilate atro-chalybeum. Vaginae delicatulae, plerumque in mucum amorphum omnino diffluentes, chlorozincico ioduralo non &nbsp;caerulescentes. Trichomata dilute purpurea, parallela, recta vel modice flexuosa, non torulosa, 4. um ad 4,8 um. crassa, apice capitala et vix attenuata arcuata vel uncinata; arliculi subquadrati vel diametro longiores, 3 um ad 6 um longi; dissepimenta saepe lineis geminis punctatis granulata; cellula apicalis calyptram depresso-conicam praebens.','Gomont 1892',NULL,0,0),(1740,2173,'description','Thallus thin, brown-purple, dried dark steel-blue or dirty violet. Filaments straight or slightly curved. Sheaths delicate, thin, mostly diffluent. Trichomes pale purple or reddish, 4-6.5(7.5) μm wide, not constricted at the often granulated cross-walls, slightly attenuated at the ends, bent and capitate. Cells nearly quadrate or longer than wide, 3-6.6 μm long. Apical cells capitate, with flat-conical calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1741,2173,'eco_distro','Benthic on stones and stony substrate in cold streams, littoral of clear lakes, and possibly also from wet soils near Alpine streams, mainly in mountains; Alpine regions, from Europe known from Alps (Austria, Italy, Switzerland); originally described from North America, where is common in clear springs and streams in high mountains.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1742,2177,'other','M. inter alias algas aquaticas repertus; fills simplicibus, elongatis et flexuosis; vaginis firmis, hyalinis, ad apicem apertis; trichomatibus multis (9-13) intra vaginam, subparallelis vel contortis, ad dissepimenta constrictis, dissepimentis non granulosis; cellulis diametro 2-3 (plerumque 2)-plo longioribus, cylindricis; protoplasmate granuloso; cellula apicali acute conica (diametro circiter 5-plo longiori). Crass, fil. 54-65 um; crass, trich. 2-7-3 um.','West &amp; West 1897',NULL,0,0),(1743,2178,'diagnosis','M. filis 30-65 um crassis, simplicibus vel parce pseudoramosis; vaginis distinctis hyalinis, vix lamellosis, usque ad 20 um crassis, chlorozincico jodurato carulescentibus; trichomatibus intra vaginam plus minusve numerosis, sæpe funiformi-contortis, 3-5 um crassis, articulis 3-8 um longis, ad genicula vix constrictis (in sicco); protoplasmate granuloso; cellulis apicalibus usque ad 13 um longis, obtuse conicis, haud capitatis, sine calyptra.','Boye-Petersen 1923',NULL,0,0),(1744,2179,'description','Thallus dark blue-green, membranaceous; filaments numerous, sheaths mucilaginous, completely diffluent; trichomes bright blue-green, 5.5-6 μm wide, not constricted; cells 1/3-2/3x as long as wide, sometimes nearly isodiametric; apical cells rounded or conical, mostly with small calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1745,2179,'eco_distro','Freshwater, periphytic on submerged stones in a rapid flowing stream; Chile.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1746,2181,'diagnosis','Stratum atro-virens, clathratum (in unico specimine viso). Fila recta, flexilia, subparalleliter aggregata. Vaginae in mucum amorphum, chlorozincico iodurato haud caerulescentem diffluentes. Trichomata pallide aeruginea, ad genicula non constricta, 4-6 um crassa apice attenuato laxe spiralia vel uncinata, capitata; articuli diametro longiores, rarius quadrati, 6-7 um longi, dissepimenta granulis protoplasmaticis vulgo notata; cellula apicalis (statu evoluto) calyptram depresso-conicam vel rotundatam praebens.','Gomont 1899',NULL,0,0),(1747,2181,'description','Thallus dark green, clathrate. Filaments straight, ± parallelly-arranged. Sheaths mucilaginous, diffluent. Trichomes pale blue-green, 4-6 μm wide, not constricted at the mostly granulated cross-walls, attenuated and slightly spirally-coiled or hooked (bent) at the ends, capitate. Cells 6-7 μm long, rarely isodiametric. Apical cells with compressed-conical or rounded calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1748,2182,'diagnosis','Stratum chalybeum plantas aquaticas limumve obducens. Fila subamorpha, fragilia. Vaginae valde mucosae, agglutinantes, chlorozincico iodurato caerulescentes. Trichomata aeruginea, in vaginis vulgo numerosa, parallela, recta, ad genicula eximie constricta, apicern versus interdum longissime attenuata, 6 um ad 10 um crassa; articuli diametro trichomatis subaequilongi, 5 um ad 10 um longi, passim doliiformes, granulis protoplasmaticis sparsis farcti; cellula apicalis conica vel cylindrato-conica, haut capitata.','Gomont 1892',NULL,0,0),(1749,2182,'description','Thallus expanded, steel to grey bluish or brownish. Filaments somewhat amorphous, fragile. Sheaths very mucilaginous, agglutinating, containing several to many trichomes. Trichomes blue-green, 6-10 μm wide, straight, parallelly-arranged, distinctly constricted at the ± translucent cross-walls, gradually attenuated at the ends. Cells weakly barrel-shaped, nearly isodiametric or 1/2-2/3x as long as wide, rarely slightly longer than wide, 3-5-10(11) μm long. Apical cells not capitate, conical or cylindrical-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1750,2182,'eco_distro','Freshwater, in flowing and stagnant waters, on mud, walls, stones, rocks and water plants, rarely in thermal springs; widely distributed in all temperate, subtropical and tropical zones; Europe: Croatia, England, France, Germany, Greece, Italy, Sweden, Switzerland, etc.; outside Europe: Brazil, China (Province Hunan), Japan.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1751,2183,'description','Thallus dark green, blue‑green to grey blue‑green, lamellated. Filaments densely aggregated or solitary among other algae, not or sparsely pseudobranched, 10‑30(50) μm wide. Sheaths colourless, hyaline, variably thick, uneven from outside, rough, occasionally diffluent, attenuated or open at the ends. Trichomes dark olive‑green or blue‑green, (1.3)1.5‑2 μm wide, 4-6 up to ± numerous within the sheaths, often seemingly loosely arranged, slightly or distinctly constricted at the usually translucent and rarely granulated cross‑walls, long-attenuated at the ends. Cells up to 3x as long as wide, rarely longer, 1.8‑6.5(8.5) μm long; cell content mostly finely granular. Apical cells long, very acute-conical, not capitate.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1752,2183,'eco_distro','Marine, on rocks, rock‑pools and algae in littoral and supralittoral zones, in salt‑marshes brines, on roots of mangroves, sometimes in inland stagnant salt waters (Czech Republic) and flowing salt water (Kazachstan ‑ f. <em>minor </em>Elenkin); common and distributed worldwide, cosmopolitan, but only in tropical and subtropical to temperate regions.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1753,2184,'diagnosis','Fila in stratum griseo-aerugineum dense intricata aut variis Algis permixta, simplicia vel parce pseudo-ramosa. Vaginae amplae, ambitu irregulares, apice acuminatae aut apertae, interdum omnino diffluentes, chlorozincico iodurato non caerulescentes. Trichomata viridi-olivacea, intra vaginam plus minusve numerosa, elongata, flexuosa, vulgo sublaxe aggregata, ad genicula eximie constricta, apice saepius longissime attenuata, 1,5um ad 2 um crass ; articuli longiores quam latiores, frequenter diametro trichomatis ad triplo longiores, 2.2 um ad 6 um longi; dissepimenta pellucida, haud raro granulala; cellula apicalis haud capilata, acuttisime conica.','Gomont 1892',NULL,0,0),(1754,2185,'description','Thr. Lager oft weit ausgebreitet, aus netzförmig anastomosirenden, haardicken Bündeln bestehend, selten hautartig-faserig, von schmutzig oliveubrauner bis braunschwärzlicher Farbe, matt glänzend. Fäden zu wenigen bis vielen in einer gemeinsamen, farblosen, nicht deutlich geschichteten Gallertscheide, 4 bis 6 um dick; veget. Zellen ungefähr so lang als breit, Endzellen stumpf abgerundet, meist etwas länger als breit.','Hansgirg 1892',NULL,0,0),(1755,2187,'description','Filaments solitary, unbranched, very long, usually straight, (16)19‑28 μm wide. Sheaths distinct, firm, colourless; open at the ends, containing 7‑12(16) trichomes, ± parallelly and densely-aggregated. Trichomes greyish blue‑green, 2‑2.8 μm wide, not constricted at the ungranulated cross‑walls. Cells longer than wide, 3.2‑5.6 μm long. Apical cells acute-conical, usually up to 10 μm long.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1756,2187,'eco_distro','Thermal springs, mostly sulphurous; Europe: Croatia, Hungary, France, and Greece (as <em>Microcoleus sociatus </em>fa.); known also from Georgia and Japan; probably sometimes differently interpreted and more widely distributed.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1757,2178,'description','Filaments with few to many loosely arranged trichomes per sheath. Sheaths colourless, unlamellated or lamellated; trichomes usually immotile, bright blue-green, tapering towards ends, unconstricted to indistinctly constricted at the cross-walls, (3.8)4-5 μm wide. Cells 3.5-9 μm wide, apical cells conical, elongated, never capitate, 7.5-12 μm long.','Boyer et al. 2002',NULL,0,0),(1758,2178,'eco_distro','Desert soils, USA','Boyer et al. 2002',NULL,0,0),(1759,1544,'diagnosis','Fila sparsim repentia, rarius in stratum nigrum et nitens intricata, tortuosa, haud raro confuse pseudo-ramosa. Vaginae cylindracae, ambitu plus minusve inaequales, agglutinantes, apice acuminatae et clausae, aut apertae et evanescentes, interdum omnino diffluentes, chlorozincico iodurato non carulescentes. Trichomata aeruginosa intra vaginam permulta, arcte congesta, plerumque funiformi-contorta, extra vaginam recta, ad genicula haud constricta, apice sublonge attenuata et capitata, 3,5 um ad 7 um crassa; articuli subquadrati, vel diametro trichomatis ad duplo breviores, rarius ad duplo longiores, 3 um ad 7 um longi; dissepimenta frequenter granulata; membrana cellulae apicalis superne in calyptram depresso-conicam incrassata.','Gomont 1892',NULL,0,0),(1760,1544,'description','Filaments solitary, creeping or forming a ± thick, sometimes membranaceous, soft, blackish green to dark blue-green, inside greyish, strand-like thallus, sparsely pseudobranched, variably curved, attenuated at the ends. Sheaths usually colourless, not lamellated, variably thick, rough, uneven, sometimes diffluent, occasionally with annular transversal constrictions, containing usually numerous, densely entangled or nearly parallelly-arranged, often rope-like contorted trichomes. Trichomes long, bright blue-green or olive-green to dirty green (also reddish?), (2.5)-3-7-(9?) μm wide, not constricted at the often granulated cross-walls, usually gradually attenuated at the ends, motile. Cells are shorter than wide, 2-5(6.7) μm long. Apical cells ± &nbsp;capitate, bluntly-rounded, with conical, obtuse-conical, or hemispherical calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1761,1544,'eco_distro','Subaerophytic, on soils, desert soils, moist walls, stones, dried mud, calcareous rocks, waterfalls, littoral of lakes, rarely submerged in stagnant and flowing waters, often in polluted localities, sometimes together with other cyanoprokaryotes (<em>Schizothrix, Porphyrosiphon</em>) forming phormidioid masses; recorded also from marine (?) or brackish (?) littorals (coasts); known from both temperate and tropical zones, probably distributed worldwide and cosmopolitan.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1762,1402,'description','Thallus elongate‑cylindrical, cespitose, gelatinous, greenish or dark green, attached to the substrate. Filaments long. Sheaths thick, widened, diffluent or delimited when young, containing few to numerous trichomes. Trichomes 14‑20(21) μm wide, pale greenish, mostly straight, sometimes slightly curved, not constricted at the cross‑walls, shortly attenuated at the ends, sometimes slightly bent. Cells very short, discoid. Apical cells usually attenuated, obtuse- or acute-conical (truncate).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1763,1402,'eco_distro','Marine, on coastal stones, walls, algae, etc., widely distributed (?); Europe: known mainly from Mediterranean region, Adriatic Sea, Aegean Sea (Greece).','Komárek &amp;Anagnostidis 2005',NULL,0,0),(1764,2190,'description','Filaments very long, usually unbranched, rarely sporadically pseudobranched at the ends, nearly straight or ± bent, up to 50 μm or more wide. Sheaths entirely diffluent, containing many trichomes, densely and parallelly-arranged in fascicles or loosely rope‑like contorted. Trichomes reddish or greenish‑reddish, very long, 1.6‑1.8 μm wide, not constricted at the translucent, ungranulated cross‑walls. Cells 2‑5x longer than wide, 3.2‑9 μm long. Apical cells acute-conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1765,2190,'eco_distro','Marine, endophytic within the <em>Codium bursa </em>thallus, described from Mediterranean Sea coasts of France (Banyuls), known also from numerous localities along the continental and island coasts of Aegean Sea, Greece (Thessaloniki, Kassandra, Piraeus, Lesbos); outside Europe known probably from subtropical Pacific coasts (Japan, Mexico).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1766,2191,'description','Cette dernière a la même teinte et le même aspect général que M. wuitneri cependant, elle en diffère très nettement par ses trichomes plus gros (1,6-1<sup>um</sup>, 8 au lieu de 1<sup>um </sup>, 2), longuement atténués vers leurs extrémités, et surtout par ses cellules apicales en forme de cône très aigu.','Frémy 1932',NULL,0,0),(1767,2193,'description','Filaments formés ordinairement d\'un grand nombre de trichomes: trichomes épais de 1.2 um non atténués vers leur sommet: articles 3 à 5 fois plus longs que larges, non rétrécis aux articulations cellule apicale à membrane supérieure arrondie, sans épaississement dépourvue de coiffe.','Frémy 1932',NULL,0,0),(1768,2192,'description','Filaments very long, unbranched, nearly straight or ± curved, up to 20 μm wide. Sheaths commonly completely diffluent, occasionally very thin, containing numerous, ± densely and nearly parallelly-arranged or rope‑like involuted trichomes in fascicles. Trichomes pinkish reddish or red, (1)1.2‑(2) μm wide, very long, not constricted at the usually translucent, ungranulated cross‑walls, not attenuated at the ends, not capitate. Cells longer than wide, frequently up to 5x longer, 4.5‑6 μm long. Apical cells cylindrical and rounded, without thickened cell walls or calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1769,2192,'eco_distro','Marine, endophytic within the thallus of <em>Codium </em>species or epiphytic on other algae, often together with other cyanoprokaryotes (<em>Microcoleus codii, Brachytrichia balani </em>var. <em>purpurea); </em>described from coasts of Mediterranean Sea in France (Banyuls), known also from Canary Islands (Tenerife) and from Pacific coast of Mexico.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1770,2195,'description','Ph. terrestre, olivaceo-myochroum, nigrum, membranaceum, radians; trichomatibus vel rectis, vel flexuosis, aequalibus (diam. 1/450´´´), hyalino-olivaceis; articulis ad genicula transversim punctatis, diametro subaequalibus; stria media tenuissima, transversali dimidiatis; apiculo attenuato, obtuso, interdum brevissime barbatulo.','Kützing 1843',NULL,0,0),(1771,2195,'eco_distro','Auf Erde in Gürten, in Schmutzwinkeln, Rinnsteinen und an den Ausflüssen der Küchen.','Kützing 1843',NULL,0,0),(1772,2196,'eco_distro','subaerophytic on various substrates, partly submersed, in temperate zones','Strunecký et al. 2013',NULL,0,0),(1773,2197,'description','Physeumatibus, tenuissimis, violaceo-coerulescentibus, e strato obscure-virente,nitido longe radiantibus. Ad &nbsp;fenestrarum &nbsp;commiasuras in vitro stillitidiis irrotato expansa. Hyeme. (Exsiccata membranam nitidam contiguam praestat, ex gua physeumata belle violacea s. coerulea prominent, ab.<em> O. auctumnali tenuitate differt.)</em>','Wallhrot 1833',NULL,0,0),(1774,2198,'description','Trichomes blue-green, 7-8 μm wide, not constricted at the cross-walls, cells 1.8-2.5 μm long.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1775,2198,'eco_distro','Marine, on <em>Griffithsia</em> in the lower littoral region; Pacific Ocean coasts (USA -California)','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1776,2199,'description','Lager krustenförmig, schmutzig spangrün, später oft verblichen, und ziemlich hart werdend. Fäden gerade oder leicht gekrümmt, sehr dünn, mit blass blaugrünem Inhalte, zu zwei oder einzeln in an den Enden fast dichotom getheilten, öfters auch zerfetzten, farblosen, meist deutlich geschichteten, bis 11 um breiten, glatten Gallertscheiden eingeschlossen.','Hansgirg 1892',NULL,0,0),(1777,2199,'eco_distro','An feuchten Felsen oder am Rande von Torfsümpfen u. ä. selten (5—11). So bei Weckelsdorf (Kirchner Algenfl. p. 245), am Rande der torfigen Sümpfe bei Habstein nächst Hirschberg','Hansgirg 1892',NULL,0,0),(1778,702,'description','Filaments firstly polarized with basal heterocytes, later joined many together into the tight and densely arranged fascicles, up to over 1 mm long; they are firstly creeping, later ± erect and usually forming small tufts with ± parallel situated trichomes, heteropolar, ± cylindrical, sometimes slightly widened at the basis and slightly widened or narrowed at the apex, without hairs, without branches, quite extraordinary only with scytonematoid false branching, usually with basal heterocytes. Sheaths thin, firm, lamellated, colourless or yellowish, open at the apex. Trichomes cylindrical or slightly narrowed in the middle part and slightly widened at the basis and at the apex, 3–6 μm wide, not constricted at cross–walls, with basal and less frequently also intercalary heterocytes. Cells cylindrical, isodiametric or slightly shorter or longer than wide, olive–green, greyish blue–green or yellowish; apical cells rounded or spherical and ± hyaline. Basal heterocytes subspherical, hemispherical, oval or oval–cylindrical, intercalar heterocytes cylindrical, usually distinctly longer than wide. Akinetes not known. Reproduction by hormogonia.','Sant Anna et al. 2010',NULL,0,0),(1779,767,'description','Many filaments ± parallely and densely arranged in erect fascicles, cylindrical, long, 8–11 μm wide, without branching. Sheaths distinct, colourless, sometimes slightly lamellated. Trichomes slightly widened at the apex, in the middle and to the basis sometimes indistinctly narrowed, in the upper part 5–6 μm wide, in narrow parts only 3 μm wide, not constricted at cross–walls, only rarely indistinctly constricted at the ends and in hormogonia. Cells blue–green, olive–green to yellowish, ± isodiametric, in meristematic zones and in hormogonia shorter than wide, in narrower parts cylindrical and up to 2× longer than wide; end cells widely rounded, sometimes more pale yellowish. Basal heterocytes ovoid, shortly barrel–shaped, hemispherical up to cylindrical–rounded; intercalar heterocytes ± cylindrical, 5–12 μm long.','Sant Anna et al. 2010',NULL,0,0),(1780,766,'description','Many filaments joined ± parallel into dense, rich fascicles; filaments 6–8 μm wide, at the basis up to 11 μm wide, ± cylindrical, long. Sheaths distinct, slightly lamellated, yellowish. Trichomes ± cylindrical, not constricted at cross–walls, sometimes very slightly widened, at the basis and towards ends, 4–6 μm wide, rarely narrowed up to 1.8 μm. Cells usually with slightly visible cross–walls, shorter than wide up to ± isodiametric, pale greyish blue–green; apical cells spherical, ± hyaline, sometimes with refractive content. Heterocytes basal, short, hemispherical, and intercalar, cylindrical, 8–11 × 3.5–5 μm.','Sant Anna et al. 2010',NULL,0,0),(1781,703,'description','Thallus green to dark green forming small moss-like strata. Young filaments isopolar, bent in the middle. Older filaments heteropolar and pseudobranched, with basal heterocysts and rarely with intercalary heterocysts. Heteropolar filaments (10) 12–18 um wide (12.3±1.2 um, n=30), isopolar filaments 10–14 mm (10.6±1.3 um, n=30). Cells shorter than wide, 6–9 um wide, 2–5 um long. Reproduction by hormogonia. Akinetes present.','Lamprinou et al. 2012',NULL,0,0),(1782,2201,'diagnosis','LM observations-Unicellular, cells solitary or agglomerated in groups (Figs A, B), but without common mucilage. Cells widely coccoid, sometimes curved or sigmoid, rounded at the ends, with a mean diameter of 2.0–3.5 μm and a length of 3–5 μm, usually pale blue-green, rarely olive-green, bright blue-green or pinkish, division always by binary fission, perpendicular to the longer axis of the cell, reproduction by solitary cells (Figs C, D). TEM observations-Cells with several dispersed or solitary polyhedral bodies, thylakoids localized along cells walls, photosynthetic pigments attached to it (Figs E, F).The new species is closely allied to S. elongatus C. Nägeli, but differs from it by having shorter cell with length 1.0–1.5 times of width, and cell length of <em>S. elongatus</em> is 1.5–3.0 times of width.','Lv et al. 2017',NULL,0,0),(1783,2202,'description','Thallus macroscopic, free-living on rocky substrates in natural conditions, violet to black-brown. In liquid culture, growing as a spherical macroscopic biomass on the bottom of the test tube. Long filaments loosely aggregated in young colonies, and always enclosed by firm mucilage layer. The young colonies eventually becoming compact macroscopic colonies with densely entangled filaments. Sheath colorless, usually visible in younger colonies. Trichomes isopolar, apical cell morphologically not different from other cells. Cells spherical to barrel-shaped. Heterocytes, spherical or oval, smaller than vegetative cells, terminal in young colonies, intercalary in old colonies. Akinetes not known. Reproduction by fragmentation of the trichomes into motile hormogonia.','Cai et al. 2020',NULL,0,0),(1784,2203,'description','In culture, growing as a spherical macroscopic biomass on the bottom of the test tube or attached to the tube walls. Long filaments loosely aggregated in young colonies, and always enclosed by firm or wide mucilage layer. The young colonies eventually becoming compact spherical macroscopic colonies, with densely entangled filaments. Sheath colorless, usually distinct at younger colony margins, and not visible in the older colonies. Cells violet to black-brown, sometimes granulated, spherical to barrel-shaped, 2.17-2.81 μm long and 1.8-2.6 μm wide (smaller than that of Nostoc-like genera). Heterocytes spherical or oval, smaller than vegetative cells, 1.15-1.85 μm long, 0.95-1.76 μm wide (smaller than that of Nostoc-like genera), terminal in young colonies, interincalary in old colonies. Akinetes not observed during three years of cultivation.','Cai et al. 2020',NULL,0,0),(1785,1466,'description','Cells solitary or in pairs during division, oval to cylindrical with widely rounded ends, 21–25.2 um wide and 21.5–39.4 um long, blue-green to yellowish, granulated. Chromatoplasma more concentrated at cell margin, with reticulate keritomization evident. Mucilaginous sheath absent. Cells dividing by transverse binary fission in a single plane. D1-D1ʹ helix identical in sequence in both operons, with a basal clamp of 6 bp, a 3ʹ unilateral bulge of 6 nt, and a large terminal loop with 16 nt. BoxB and V3 helices differing in sequence and structure between both operons and from helices present in <em>Cyanothece svehlovae</em>.','Mareš et al. 2019',NULL,0,0),(1786,2204,'description','Cells solitary or in pairs during division, occasionally in small aggregates, oval to shortly cylindrical with widely rounded ends, 10.0–14.5 um wide and 13.5–23 um long, blue-green to yellowish, containing granules. Chromatoplasma more concentrated at cell margin, but reticulate keritomization sometimes visible. Mucilaginous sheath absent. Cells dividing by transverse binary fission in a single plane. All secondary structures of conserved domains differing between operons. D1-D1ʹ helix, with a basal clamp of 5–6 bp, a 3ʹ unilateral bulge of 5–6 nt, and a large terminal loop with 14–15 nt. BoxB and V3 helices differing in sequence and structure between both operonsand from helices present in C. aeruginosa. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1787,2204,'diagnosis','On average, smaller cells than both <em>Cyanothece aeruginosa</em> and <em>C. major</em>, which have also been reported from Antarctica. Terrestrial on lichen vegetation, while <em>C. aeruginosa</em> and <em>C. major</em> are aquatic in the original sense. Secondary structures of conserved domains of the ITS region all differing from those in <em>C. aeruginosa</em> SAG 87.79, but especially notable in the shorter length of the V3 helix in both operons. Significantly larger cells than <em>C. epiphytica</em>, which was found in a similar microhabitat (on mosses in Himalaya). Neither halophilic (<em>C. halobia</em>, <em>C. shiloi</em>) nor planktonic (<em>C. lineata</em>).','Mareš et al. 2019',NULL,0,0),(1788,2204,'etymology','Named in honor of Dana Švehlová, the technical assistant of Prof. Jiří Komárek, who has made much of the recent progress in cyanobacterial taxonomy possible.','Mareš et al. 2019',NULL,0,0),(1789,2205,'description','Colonies consisting of small cell clusters joined into a gray-green to olive-green smooth macroscopic gelatinous mass covering the substrate, 14–36 um long by 12–28 um wide. Mucilaginous envelopes wide, colorless, with 1–2 diffluent, often scarcely visible, concentric lamellations around small clusters of cells. Cells oval to cylindrical, mostly in groups of 4–8, rarely solitary, 5–6 um wide, 6–14 um long, with dividing cells 9–12 um long. Cell contents weakly pigmented, grayish olive to yellowish olive colored, mostly homogenous, sometimes minutely granular. No large storage granules visible in TEM. Secondary structure of the D1-D10 helix having a terminal loop of 13 nucleotides and two adenine residues on the 50 strand opposite the unilateral bulge on the 30 strand, with BoxB helices and V3 helices being unique among all species for which ITS sequence is available at present. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1790,2205,'diagnosis','Similar to <em>Gloeothece palea</em> and <em>G. rupestris</em>, but differing from those species by greater cell dimensions, absence of yellow pigments in the mucilaginous envelopes (based exclusively on culture observation), and origin in an equatorial tropical habitat in Africa.','Mareš et al. 2019',NULL,0,0),(1791,2206,'diagnosis','Cells mostly subspherical to widely oval, typically with a lower length:width ratio than any other <em>Gloeothece</em> species. Golden-yellowish pigmentation in the layer of mucilage immediately surrounding the cells.','Mareš et al. 2019',NULL,0,0),(1792,2206,'description','Small cell clusters joined into yellow-brownish, macroscopic, irregularly subspherical gelatinous colonies growing on the substrate surface. Envelopes around cells wide, mostly colorless, sometimes infused with golden-yellow pigment in the layer of mucilage immediately surrounding the cells, with 1–2 nearly diffluent, often scarcely visible, concentric lamellations around small clusters of cells, with an outer mucilage that is soft but not diffluent. Colonies 13–34 um long by 10–24 um wide. Cells mostly in groups of 2–8, rarely solitary, 4–4.5 um wide, 5–6 um long, with dividing cells 7 um long. Cell contents weakly pigmented, pale olive colored, mostly homogenous. No large granules visible in TEM. Secondary structure of the D1-D10 helix having a terminal loop of 12 nucleotides and a single cytosine residue on the 50 strand opposite the unilateral bulge on the 30 strand, with D1-D1ʹ, BoxB, and V3 helices having closest sequence and structural similarity to these structures in G. reniformis, but still being unique among all species for which ITS sequence is available at present. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1793,2207,'diagnosis','Similar to <em>Gloeothece palea</em> and <em>G. aequatorialis</em> in cell dimensions, but differing from those species by posessing densely packed colonies with limited mucilage, and rare occurrence of distinct individual sheaths around solitary cells or small clusters of cells.','Mareš et al. 2019',NULL,0,0),(1794,2207,'description','Colonies when young densely packed with cells not separated by individual sheaths, but possessing soft mucilage not extending more than 3 um beyond outer margin of cell cluster, with densely granular cells blue-green in color. Colonies when mature with cells more loosely aggregated in colonial mucilage extending up to 5 lm beyond outer margin of individual cells or the cell cluster, sometimes with individual sheaths evident, rarely with a single lamallate layer, with nongranular pale grayish blue-green cytoplasm. Mucilage soft but usually defined, sometimes diffluent, colorless, never yellowish. Cells oval to oval-elliptical, slightly irregular in shape when compressed in colony, 5.2–6.7 um wide, 6.2–11.2 um long, with dividing cells 9.6–12.5 um long. Secondary structure of the D1-D1´ helix having a terminal loop of three nucleotides and four residues (5ʹ–AACA–3ʹ) on the 5 0 strand opposite the unilateral bulge on the 30 strand, with D1-D1ʹ, BoxB, and V3 helices having very close structural similarity to these same structures in<em> Gloeothece tepidariorum</em>, but differing in sequence, particularly in the terminal loops.','Mareš et al. 2019',NULL,0,0),(1795,2208,'diagnosis','No mucilaginous structure observed in this species in contrast to all other known <em>Gloeothece </em>species. Cells frequently reach lemon-like shape before division. Note: observations are based exclusively on culture material.','Mareš et al. 2019',NULL,0,0),(1796,2208,'description','Cells solitary, unable to float in liquid medium. Mucilaginous envelopes absent. Cells broadly oval, with some lemon-shaped or slightly arcuated, 7–12 um long, with longer dividing (constricted and/or with crosswall forming) cells 11–15 um long, 4.7–8.0 um wide, pale grayish green, cell content finely granular. No large granules visible in TEM. Secondary structure of the D1-D1´ helix markedly different between operons, with the helix from the operon with tRNA<sup>Ile</sup> being unique among Gloeothece species thus far sequenced by having a basal clamp of 5 bp instead of four, and the smallest number of nucleotides (only 7) in the unilateral bulge on the 3´ strand. The D1-D1ʹ helix from the operon with no tRNA genes is distinct from all other Gloeothece species for which this operon was recovered in the presence of a second unilateral bulge on the 3ʹ strand (5ʹ–ACAU–3ʹ). BoxB and V3 helices distinct from all other Gloeothece species. V3 helix absent in the operon with the tRNA<sup>Ile</sup> gene.','Mareš et al. 2019',NULL,0,0),(1797,2210,'description','Reference strain: Colonies 12–20 um long by 10–18 um wide, in rapidly growing culture smaller, compact colonies with 8–16 cells. Sheath wide, colorless, with a single lamellation around small clusters of cells contained within one colony, rarely up to two concentric layers, with an outer mucilage that is distinctly delimited to almost diffluent. Cells mostly in groups of 2–4, but up to 16, 4.5–6–(8) um wide, 5.6–9 um long, with longer dividing (constricted, and/or with crosswall forming) cells up to 11 um long. Cell contents finely to coarsely granular. Secondary structure of the D1-D1´ helix having a terminal loop of three nucleotides and four residues (5ʹ–AACA–3ʹ) on the 5´ strand opposite the unilateral bulge on the 30 strand, with D1-D1ʹ, BoxB, and V3 helices having closest sequence and structural similarity to these structures in <em>Gloeothece reniformis</em>, but still being unique among all species for which ITS sequence is available at present. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1798,2211,'diagnosis','Cells frequently divide unevenly, reaching a kidney-like shape just before division, and producing daughter cells in a mirrored-diagonal position.','Mareš et al. 2019',NULL,0,0),(1799,2211,'description','Small cell clusters joined into olivegreen to brownish, macroscopic, irregularly subspherical gelatinous colonies growing on the substrate surface. Envelopes around cells wide, colorless to yellow-brown, with a single or no lamellation around small clusters of cells contained within one colony, with inner lamellation distinct to diffluent, with an outer mucilage that is distinctly delimited. Colonies 14–28 um long by 9–24 um wide. Cells mostly in groups of 4–8, but up to 16, 5–6 um wide, 8–10.5 um long, with longer dividing (constricted and/or with crosswall forming) cells up to 11 um long, with division uneven to produce kidney-shaped structures when dividing. Cell contents pale yellowish olive color, finely to coarsely granular. Medium-sized granules (mostly cyanophycin) visible in TEM. Secondary structure of the D1-D1´ helix having a terminal loop of 11 nucleotides and two nucleotides on the 5´ strand opposite the unilateral bulge on the 3´ strand in the operon with no tRNA<br>gene, a terminal loop of 13 nucleotides and one cytosine on the 50 strand opposite the unilateral bulge on the 3´ strand in the operon with the tRNA<sup>Ile</sup> gene, with D1-D1ʹ, BoxB, and V3 helices having closest sequence and structural similarity to these structures in <em>Gloeothece aurea</em>, but still being unique among all species for which ITS sequence is available at present. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1800,2214,'description','<em>Description of the strains examined in this study</em>: Sheath wide, colorless, rarely with some yellowish coloration in a few colonies, with (0)–1–4 concentric lamellations around small clusters of cells contained within one colony, with an outer mucilage that is distinctly delimited to almost diffluent. Colonies 15–40 um long by 12–26 um wide. Cells mostly in groups of 2–8, but up to 32, 4.0–5.4 um wide, 5–9 um long, with longer dividing constricted, with crosswall forming) cells up to 12 um long. Cell contents blue-green, finely to coarsely granular. Secondary structure of the D1-D1´ &nbsp;helix having a terminal loop of 5 nucleotides and four residues (5ʹ–AACA–3ʹ) on the 5´ strand opposite the unilateral bulge on the 30 strand, with D1-D1ʹ, BoxB, and V3 helices having very close structural similarity to these same structures in <em>Gloeothece bryophila</em>, but differing in sequence, particularly in the terminal loops and central helix. The presence of nifD gene confirmed.','Mareš et al. 2019',NULL,0,0),(1801,2215,'diagnosis','Larger cells than any other <em>Gloeothece </em>species except<em> G. baileyana</em> and <em>G. verrucosa</em>, from which it is distinguished by cells being distributed in a delimited but diffluent mucilage lacking visible lamellation, surface structures, or pigmentation (based exclusively on culture observation).','Mareš et al. 2019',NULL,0,0),(1802,2215,'description','Colonies consisting of irregularly arranged cells in large mucilaginous investment joined into macroscopic dark-brown floating gelatinous mats. Mucilage colorless, without visible lamellation or envelopes around individual cells or small colonies. Cells dividing by transverse binary fission in a single plane, 8–10 um wide, 8–12 um long. Cell contents pale to dark brownish-green or brown, mostly homogenous, sometimes granulated. No large granules visible in TEM. Secondary structure of the D1-D1´ &nbsp;helix having a terminal loop of 11 nucleotides and five residues (5ʹ–AAAAA–3ʹ) on the 5´ &nbsp;strand opposite the unilateral bulge on the 3´ strand, with D1-D1´, BoxB helices similar to those in <em>G. verrucosa</em>, with a V3 helix unique among all species for which ITS sequence is available at present.','Mareš et al. 2019',NULL,0,0),(1803,2215,'etymology','Named for the Tonkin region of Vietnam','Mareš et al. 2019',NULL,0,0),(1804,2216,'diagnosis','Larger cells than any other <em>Gloeothece </em>species except G. baileyana, which however has blueish envelopes; also distinguished from other taxa by the rusty yellow-brown envelopes with delicate warts on their surface.','Mareš et al. 2019',NULL,0,0),(1805,2216,'description','Colonies consisting of small cell clusters joined into larger, olive-green to brownish macroscopic irregular gelatinous mats or flocks, 16–36 um long by 12–28 um wide. Envelopes wide, colorless near cells, unevenly infused with a rusty brownish-yellow pigment, with 1–2 nearly diffluent, often scarcely visible, concentric lamellations around small clusters of cells, with an outer mucilage that is minutely warty. Cells mostly in groups of 2–8, rarely solitary, 6–8 um wide, 9–18 um long, with dividing cells 14–20 um long. Cell contents weakly pigmented, dirty olive colored, mostly homogenous, sometimes minutely granular. No large granules visible in TEM. Secondary structure of the D1-D1´ helix having a terminal loop of 10 nucleotides and five residues (5ʹ–AACGA–3ʹ) on the 5´ strand opposite the unilateral bulge on the 3´ strand, with a BoxB helix similar to that in <em>G. tonkinensis</em>, with a V3 helix uniquely shorter than in all other species for which ITS sequence is available at present.','Mareš et al. 2019',NULL,0,0),(1806,1392,'diagnosis','Differing from all other species by the complete absence of oval or elongated cells. Percent dissimilarity based on aligned ITS sequences among strains in the genus &lt;0.6%, percent dissimilarity to other species in the genus 12.5%–19.0%.','Mareš et al. 2019',NULL,0,0),(1807,1392,'description','Cells mostly solitary in nature, but also producing cell aggregates through production of mucilage, spherical, 2.5–6 lm in diameter. Confirmed diazotroph. Secondary structure of the D1-D1ʹ helix with a single adenosine residue on the 5´ strand opposite the basal unilateral bulge on the 3´strand, and with a subterminal 3´ unilateral bulge characteristic of both <em>Crocosphaera </em>species and <em>Zehria floridana</em>. BoxB and V3 helices distinct from all other <em>Crocosphaera </em>species.','Mareš et al. 2019',NULL,0,0),(1808,1392,'etymology','In honor of Stanley W. Watson, American marine microbiologist','Mareš et al. 2019',NULL,0,0),(1809,2217,'diagnosis','Differing from all other species by the production of markedly elongate cells in stationary phase which can exceed a 3:1 length-to-width ratio, and also through the production of short temporary chains of cells. Also with a D1-D10 helix shorter in nucleotides than in all other species. Percent dissimilarity based on aligned ITS sequences among strains in the genus = 0.0%, percent dissimilarity to other species in the genus 12.5%–18.8%.','Mareš et al. 2019',NULL,0,0),(1810,2217,'description','Cells solitary and spherical in exponential phase, without mucilage production or clumping, with dispersed thylakoids in fasciculated packets, 3.3–4.4 um in diameter, becoming thin and elongated in stationary growth phase, often medianly constricted, clumping in small aggregates without visible mucilage, sometimes forming short chains, 1.2–1.8 um wide, 2.8–7.1 um long. Secondary structure of the D1-D1ʹ helix shorter than in all other <em>Crocosphaera </em>species, lacking the subterminal 3ʹ unilateral bulge and with nucleotides on the 5´ strand opposite the basal unilateral bulge on the 3´ strand. BoxB helix most similar in structure to that in <em>C. watsonii</em>, but with four nucleotide substitutions and two fewer nucleotides in the terminal helix.','Mareš et al. 2019',NULL,0,0),(1811,2218,'diagnosis','Most similar to <em>Crocosphaera watsonii</em>, particularly in exponential growth phase, but differing from that taxon through the production of cylindically elongated cells in stationary phase. Also with a uniquely long and branched D1-D1´ helix unique among all cyanobacteria for which ITS structure analysis have been completed. Percent dissimilarity based on aligned ITS sequences to other species in the genus 14.3%–19.0%.','Mareš et al. 2019',NULL,0,0),(1812,2218,'description','Cells spherical to cylindrically elongated, with clumping not observed, with dispersed thylakoids in fasciculated packets, 3.0–4.4 um wide, 3.7–6.7 um long. Secondary structure of the D1-D1ʹ helix highly unusual, with terminal branching in the helix and a large unpaired loop in central helix. BoxB helix identical in length to that of <em>Crocosphaera </em>species, but differing at the terminus.','Mareš et al. 2019',NULL,0,0),(1813,2219,'description','Lager büschelig-rasenförmig, stahlblau bis schwärzlichblaugrün. Fäden zu 2 bis vielen parallel verlaufend, gekrümmt, ungleich (4.5 bis 10 um) dick, mit 4.5 bis 6 um breiten und ebenso langen oder an dickeren Fäden mit 6 bis 10 (seltener mehr) um dicken, 1/3 bis 1 mal so langen, blau- oder olivengrün gefärbten Zellen, in einer weiten, meist 25 bis 56 um breiten], farblosen, oft geschichteten und quer gestreiften Scheide eingeschlossen. Einzelne Bündel sind 2 bis 5 mm lang.','Hansgirg 1892',NULL,0,0),(1814,2219,'eco_distro','mountain streams, fast flowing water; near Tuchoraz, Český Brod and Krkonoše Mts.','Hansgirg 1892',NULL,0,0),(1815,911,'diagnosis','Stratum natans, valde expansum, laete aeruginosum. Trichomata dilute aeruginea, in totum recta, fragilia, ad genicula haud constricta, 4 um ad 6 um crassa, aetate provecta ad apicem sensim et longe attenuata obtusa capitata; articuli subquadrati vel diametro fere ad duplo breviores, 2,5 um ad 3,5 um longi, saepe protoplasmate refringente, grosse granuloso farcti; dissepimenta granulata; cellula apicalis paululum attenuata, truncata, calyptram convexam praebens.','Gomont 1892',NULL,0,0),(1816,911,'eco_distro','near the pools; Sweden (Lund) and France (Croisic)','',NULL,0,0),(1817,898,'diagnosis','Trichomata mobilia, aut singula inter ceteras algas planctonicas natantia, aut plurima strata stro-aeruginosa vel chalybeo-viridia limo affixa efformantia, elongata, plusminusve recta vel paulum flexuosa, apicibus non attenuatis nec curvatis vel capitatis, ad dissepimenta haud constricta, 5-6 µ crassa; cellulis diametro trichomatis 2-3-plo brevioribus, 2-3 µ longis; dissepimentis tenuibus plerumque sine granulis aut interdum indistincte granulatis; protoplasto chalybeo-aeruginoso vel aerugineo-viridi, cum chromatoplasmate saturate et centroplasmate parum colorato sed plus minus grosse reticulato-clathrato et vacuolis gaseosis destituto; cellula apicali obtuse rotundata, calyptra nulla.','Skuja 19565',NULL,0,0),(1818,874,'description','Trichomes mostly solitary, free-floating, up to 300 μm long, straight or somewhat curved, sometimes joined to blue-green or olive-green, microscopic, loose fascicles, occasionally forming benthic membranaceous coat (thallus), without sheaths, or very rarely and facultatively, especially in young stages, with fine sheaths. Trichomes (2.3)4-6(9.8) μm wide, immotile, not constricted (or very slightly constricted) at the granulated cross-walls, ± gradually attenuated at the ends. Cells shorter than wide or frequently isodiametric, up to 2x longer than wide (before division); cell content blue-green, with numerous aerotopes, without PE. Apical cells convex, sometimes bluntly-conical or ± pointed, sometimes with convex calyptra, rarely capitate.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1819,874,'eco_distro','Freshwater, planktic in lakes and ponds, often forming water blooms, widely distributed in temperate zones','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1820,875,'description','Trichomes solitary, free-floating, blue-green, usually straight, constricted at cross-walls, narrowed towards ends; cells with aerotopes, 2-3 x 9-10 μm, apical cells with oval calyptra.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1821,875,'eco_distro','Described from plankton of saline Aral Sea (Kazakhstan/Uzbekistan).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1822,876,'description','Trichomes solitary, free-floating in phytoplankton in vegetative state, but often developing in benthos at the beginning of the vegetation period, forming blackish blue-green or dark greenish strata on mud; trichomes ± straight or slightly flexuous, slightly constricted at cross-walls, cylindrical, not attenuated towards ends, 5-6.5(8-9?) μm wide, slightly motile. Cells always shorter than wide, 2-3 μm long, blue-green, with aerotopes. Apical cells cylindrical, widely-rounded, without calyptra or thickened cell walls.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1823,876,'eco_distro','Freshwater, benthic and planktic in lakes; known from lakes in Sweden and northern and central Germany.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1824,877,'description','Filaments solitary, free-floating, very rarely with fine and slightly visible sheaths, which develop well only in culture. Trichomes cylindrical, sometimes a little complanated from sides, blue-green, (5)6.5-7.5(9.5) μm wide, slightly constricted at cross-walls, not attenuated towards the ends. Cells usually shorter than wide, with numerous aerotopes. Apical cells widely-rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1825,877,'eco_distro','Freshwater, planktic in lakes; known only from Germany.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1826,878,'description','Trichomes solitary, free-floating, (5)6-8(11) μm wide, blue-green, straight or slightly-arcuated, not or very slightly constricted at the cross-walls, gradually (rarely abruptly) narrowed towards the ends (at the ends 3.5-4 μm wide) and roundly-obtuse at the end; cells 2.5-4 μm long with fine, facultative aerotopes.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1827,878,'eco_distro','Freshwater or slightly halophilic, planktic, described from Aral Sea, occurs in Kazakhstan and in reservoirs in desert areas of central Asia.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1828,888,'description','Colour: blue-green, trichome-width: (5)5.5-10 µm; trichome ends cylindrical, not attenuated, or very slightly attenuated; apical cells cylindrical, widely rounded.&nbsp;','Komárek &amp; Komárková 2004',NULL,0,0),(1829,888,'eco_distro','eutrophic (to hypertrophic) reservoirs','Komárek &amp; Komárková 2004',NULL,0,0),(1830,908,'diagnosis','Trichomata ± recta,solitaria, varie longa, libere natantia, apice nec attenuata nec curvata, ad genicula vix vel lenissime constricta, 6-9.5 um crassa, cellulis plerumque ,paulo brevioribus (1/3-3/4) quam latioris, raro isodiametricis; protoplasto dilute aeruginoso, medio contentu refringente, grosse granuloso vel vacuolis gaseosic farcto; cellula apicali superne convexa, truncato-rotundata, interdum cum membrana incrassata; calyptra nulla.','Skuja 1948',NULL,0,0),(1831,903,'description','Trichomes solitary, in flocculant mass or in clusters, pale blue-green, usually free‑floating, straight or wavy, distinctly constricted at cross‑walls, 10‑15 μm wide, narrowed towards ends and usually slightly arcuated. Cells finely granulated, 2‑6.5 μm long, with one or few large, flattened oval aerotopes, which can be missing in parts of trichomes. Apical cells rounded‑conical, without thickened outer cell walls or without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1832,903,'eco_distro','Freshwater, planktic, free-floating in lakes and small water bodies, described from Burma and known rarely from tropical Asia (e.g., Pakistan) and Africa, maybe also from southern Europe (Mediterranean region);','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1833,880,'description','Trichomes solitary, rarely in small loose clusters, cylindrical, 7.5-10(11.5) μm wide, in the middle straight or irregularly wavy and coiled, and particularly at the apices loosely spirally-coiled, not attenuated or rarely slightly attenuated at the ends, but sometimes straight at the ends or loosely screw-like coiled along the whole length, blue-green, finely but distinctly constricted at the cross-walls. Cells ± 1/4 as long as wide, 2.4-3.4 μm long, with densely arranged aerotopes, up to isodiametric. Apical cells convex, widely rounded, without calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1834,880,'eco_distro','Freshwater, developed in littoral of reservoirs, later planktic, in lakes; Europe: Czech Republic, S Russia, Ukraine.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1835,883,'description','Trichomes straight or curved, 2-5(5.8) μm wide (always less than 6 μm), seldom solitary, mostly forming purple-red, dirty purple (when dried violet), irregular and loose flakes (groups) or bundles, not constricted at often granulated cross-walls, gradually attenuated at the ends, ± motile (facultatively?). Cells reddish or pinkish-violet, nearly isodiametric or rarely longer or shorter than wide, 4-6 μm long, with aerotopes. Apical cells capitate, obtuse-conical, usually with calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1836,883,'eco_distro','Freshwater, planktic in colder lakes and stagnant waters, forming red water blooms; Europe: Denmark, England, Germany, Hungary, S Norway, Sweden; outside Europe: commonly distributed in North America','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1837,904,'other','Stratum natans, valde expansum, conspicue purpureum (sec. auct.), in speciminibus siccis amoene lilacinum. Trichomata in tolum recta, elongata, flexilia, ad genicula haud constricta,aetate provecta ad apicem sensim et longe attenuata obtusa capilata, 2,2 um ad 5 um crassa; articuli subquadrati vel diametro paulo longiores, 4 um ad 6 um longi, cunctis, apicalibus exceptis, protoplasmate refringenti, grosse granuloso farcti; dissepimenta frequenter granulata; cellula apicalis paululum attenuata, truncata, calyptram depressoconicam praebens.','Gomont 1892',NULL,0,0),(1838,893,'description','Trichomes are pale blue-green or yellow-green. Trichomes are solitary and they float, they sometimes become entangled and sink to the bottom of culture tubes, but they never attach there. They are straight or slightly curved, sometimes attenuated towards the ends and not surrounded by sheath under conditions favourable for growth. Cross-walls may be slightly constricted or not constricted and not granulated. Gas vesicles are relatively large and scattered at the periphery of the cells. Apical cells show variable shapes such as rounded, tapered, bluntly conical, occasionally capitate, with and without calyptra. Cell dimensions are 3±0–6±4 µm wide, 1±2–4±2 µm long and the ratio of cell length to width is about 1: 3–1: 1. PE is absent. Not capable of complementary chromatic adaptation. Fatty acid composition is type 2B. DNA G­C content is about 40 mol%. Growth temperature range is 20–30 °C. Salinity up to 0±78% is tolerated for growth. 16S rDNA sequence is the only distinguishing character between P. agardhii and this species.','Suda et al. 2002',NULL,0,0),(1839,742,'description','Trichomes are pale blue-green or yellow-green. Apical cells are rounded, more or less tapered, bent but not pointed, bluntly conical and have no calyptra. Cell width is 5±4–2±2 µm, cell length is 1±7–6±7 µm and the ratio of cell length to cell width is 2: 7–1: 1. On occasion, thick sections are found in a single trichome in both lab cultures and field samples. Growth temperature range is 20–30 °C; some strains grow at 40 °C. Salinity up to 0±78% is tolerated for growth.&nbsp;','Suda et al. 2002',NULL,0,0),(1840,885,'description','Trichomes straight or slightly curved, solitary, free-floating, sometimes forming purple-red (when dried violet) free-swimming irregular clusters and water blooms, without sheaths (very fine sheaths can appear only in culture), pale purple-red, (3.9)6-8(9.4) μm wide, facultatively slowly motile, without rotation, not constricted at the sometimes granulated cross-walls, gradually attenuated to the ends. Cells nearly isodiametric, or slightly longer or shorter than wide, after the division 1/2-1/3x as long as wide, 2-4(5) μm long, with numerous aerotopes, with large amount of PE. Apical cells rounded, tapered, bluntly conical, rarely capitate, with convex calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1841,885,'eco_distro','Freshwater, planktic, in mesotrophic and eutrophic, large lakes and stagnant waters, forming red water blooms; cold water form, often in winter colouring the water red under the ice; it occurs in several regions in northern temperate zone with obligatory distribution','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1842,905,'other','Stratum natans, valde expansum, submembranaceurn, amelhysteo-rubescens (sec. auct.), in speciminibus siccis amoene lilacinum. Trichotnata in totum eximie recta, rigida, fragilia, ad genicula haud constricta, aetate provecta ad apicem sensim et longe attenuata, obtusa, leviler capitata, 6 um ad 8 um crassa. Articuli diametro trichomatis duplo ad triplo breviores, 2 um ad 4 um longi, cunctis, apicalibus exceptis, protosplasmate refringenti, grosse granuloso farcti; dissepimenta frequenter granulata; cellula apicalis paululum attenuata, truncata, calyptram convexam praebens.','De Candole ex Gomont 1892',NULL,0,0),(1843,887,'description','Trichomes solitary, free-floating (suspended among other algae), only in old cultures tending to accumulate near the surface, blue-green, yellow-green or olive-green, cylindrical, up to several mm long, straight or slightly curved, 2-4 μm wide, not or sometimes very slightly constricted at the ends. Cells nearly isodiametric or somewhat longer or shorter than wide (after division!); cell content with numerous large and characteristically elongated aerotopes. Apical cells mostly longer, up to 6 μm long, nearly hemispherical up to rounded-conical, with only 2-3 aerotopes, sometimes calyptrate. Little known species.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1844,887,'eco_distro','Freshwater, planktic in mesotrophic to eutrophic reservoirs, described from \'Kiessee\' by Göttingen in Germany, known also from Czech Republic, probably more widely distributed in temperate zone.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1845,886,'description','Trichomes single, floating, straight, olive-blue-green, cylindrical, not constricted at cross-walls, 2.5-3.5 μm wide, not attenuated towards ends, apical cells cylindrical-rounded; 1-3 aerotopes in each cell.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1846,886,'eco_distro','polluted pond in Pakistan (Peshawar)','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1847,1880,'description','Thallus soft, spongy, membranaceous, yellow; filaments (10)13.5- 14.5(15) μm wide; sheaths firm, thick, yellow to brown, sometimes layered; trichomes blue-green, 8.5- 9.5 μm wide, slightly constricted; cells isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1848,1880,'eco_distro','On moist soil and wet rocks; Angola, India (Assam).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1849,1882,'description','Filaments initially aggregated into clusters, later fused into extensive, 0.5-2 mm thick, greyish-blackish thallus (mats); incrusted with calcium carbonate; sheaths about 2 μm thick, brown; trichomes blue-green, 4 μm wide, not constricted; cells 6-10 μm long.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1850,1882,'eco_distro','On bark of trees and walls; tropical species, India (Calcutta).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1851,1884,'description','Thallus olive-green, violet or red, filaments 10-14 μm wide, sheaths colourless, lamellated, when older often red; trichomes blue-green or violet, 8-12 μm wide, constricted or unconstricted, cells isodiametric or shorter than wide.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1852,1884,'eco_distro','On moist soils, mosses, and in stagnant waters; probably pantropical, occurs in numerous tropical regions.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1853,1888,'description','Thallus ± expanded, compact, tomentose, moistened grey-brown, dried brown to black, filaments 9.6-11(13.2) μm wide, sheaths up to 3 μm wide, usually colourless and unlamellated, but when old brownish, lamellated, trichomes yellow or brown, (6.6)9-10(12) μm wide, not or somewhat constricted, cells 4-6-8 μm long.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1854,1888,'eco_distro','Subaerophytic, on the bark of trees and moist soils, India.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1855,1896,'description','Thallus membranaceous, red-brown; filaments 8-16 μm wide, sheaths red-brown or hyaline, trichomes 7-10 μm wide, cells ± isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1856,1896,'eco_distro','Aerophytic, at bases of trees; New Guinea.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1857,1910,'description','Filaments 11-12 μm wide, sheaths thick, brown or red, sometimes colourless, cells nearly as long as wide or 1/2x as long','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1858,1910,'eco_distro','On rocks, Samoa Islands.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1859,1897,'description','Thallus expanded, dark red or dull violet, sheaths firm, thick, blue-reddish or purple, trichomes 3-4 μm wide, not constricted, cells quadrate or shorter than wide.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1860,1897,'eco_distro','On moist soils near Lahore, India.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1861,1903,'description','Filaments up to 6 μm wide. Sheaths thick, yellow-brown, slightly lamellated, smooth at the surface. Trichomes about 3 μm wide, slightly constricted at cross-walls. Cells 2-3x shorter than wide, apical cells rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1862,1903,'eco_distro','Subaerophytic on rocks, mainly in mountains in Europe: Slovakia (High Tatra Mts.).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1863,1905,'description','Thallus leathery, somewhat gelatinous, yellowish brown to olive-green, when dry often violet. Filaments densely entangled, up to 9 mm wide. Sheaths colourless, smooth, at first thin, later up to 3 μm thick and lamellated. Trichomes olive-green, 2.5-6 μm wide, not constricted at the often granulated cross-walls, not attenuated at the ends. Cells isodiametric to 1/3x as long as wide, 1.5-5.5 μm long. Apical cells rounded, with hardly visible rounded calyptra.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1864,1905,'eco_distro','Marine, common on coastal rocks (mainly in upper zone); rock-pools, stones, walls, on various algae and cyanoprokaryotes, also in littoral of salty and brackish waters, marshes and estuaries; records from thermal (salty?) springs must be revised; distributed worldwide, probably cosmopolitan.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1865,1912,'description','Filaments nearly straight, 12-12.5 μm wide, sheaths firm, colourless, lamellated, trichomes bright blue-green, 8.5-9.5 μm wide, not constricted at cross-walls; cells 2-2.4 μm long, apical cells conical.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1866,1912,'eco_distro','Stagnant waters, among other algae; Antarctica','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1867,833,'description','Filaments entangled, joined to fascicles, 14-18 μm wide; sheaths colourless, trichomes pale blue-green, 7-10 μm wide, constricted at cross-walls.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1868,833,'eco_distro','Freshwater, described from a stream in E Africa','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1869,834,'description','Filaments live solitary or in small groups, 4.4-7.8 μm wide, composed of thin, colourless sheaths, which are sometimes slightly telescopically widened at the ends, and short trichomes; variously coiled and flexuous. False branching not very common. Trichomes not constricted at cross-walls, slightly attenuated towards ends, sometimes screw-like coiled within sheaths. Cells greyish or yellowish blue-green, shorter than wide, 1.1-2 μm long, in the middle 3.8-6.8 µm, near the apex 2.6-4.0 μm wide.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1870,834,'eco_distro','Freshwater, endogloeic, in the mucilage of <em>Batrachospermum</em>; S Poland (Carpathian region).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1871,854,'diagnosis','Filamentis pro rata parte brevibus (ad 2 mm), flexuosis, solitariis vel binis - quaternis, sed stratum non formantibus, in muco inter frondes <em>​Batrachospermi &nbsp;</em>viventibus. Pseudoramis geminis vel solitariis, obliguae erempentibus. Vaginis hyalinis, tenuibus, non lamellosis, infra apicem interdum contraherentibus, apice laciniatis et diffluentibus, chlorozincico joduratonon coerulescentibus. Fila in media parte 4.9-7.8 um, saepius 6.2-6.7 um lata, sub apice 4.4-5.5 um lata. Trichomatibus caesio vel flavo aeruginosis, in utroquae apice leaviter attenuatis, ad genicula non constrictis, media in parte 3.8-6.8, saepius 4.4-5.4 um latis, sub apice 2.6-4, saepius 3-3.3 um latis. Cellulae 2-3-plo diametro trichomatis breviores, saepius 1.1-2.2 um longae, contentu tenuiter granulato, ad dissepimenta non granulato; cellula apicalis rotundata, rarius depresso subconica. &nbsp;Propagatio hormogoniis et fragmentatione filorum, interdum in cellulas solitarias.','Starmach 1957',NULL,0,0),(1872,854,'eco_distro','near Krynica - Poland,','Starmach 1957',NULL,0,0),(1873,521,'diagnosis','Fila badia, dense intricata, trichomis plerumque una vel raro duabus, &nbsp;usque ad 2.5 um lata. Vagina fulginosa, firma, laevis, aperta, &nbsp;fulginosa. Trichoma constricta ad septa, non descrescentes, cellulis &nbsp;apicalibus obtuse rotundis, 1.0-1.3 um latae. Cellulae nongranulatae, &nbsp;subaeruginosae, 2.0 um longae.','Johansen et al. 2008 (sub L. badia)',NULL,0,0),(1874,835,'description','Thallus blackish or brownish green. Filaments long, flexuous, richly and repeatedly falsely branched, usually with two pseudobranches, which are usually narrower than the main filament. Sheaths colourless, fairly thick in main filaments. Trichomes pale blue-green, 2-3.5 μm wide, constricted at cross-walls, slightly attenuated towards ends. Cells always shorter than wide, cell content homogeneous, apical cells rounded, without calyptra.&nbsp;','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1875,835,'eco_distro','Marine, epilithic in littoral water level zone','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1876,866,'diagnosis','Stratum nigro vel fusco-viride. Fila elongata, flexuosa, abundanter, etiam repetite pseudo-ramosa; pseudo-rami vulgo geminati, elongati, filo primario tenuiores. Vaginae hyalinae, in filo primario crassiusculae, chlorozincico iodurato haud caerulescentes. Trichomata dilute a3euginea, brevi-articulata, torulosa, 2-3,5 um crassa, apice subattenuata; articuli diametro usque ad quadruplo breviores; protoplasma homogeneum; cellula apicalis rotundata.','Gomont 1899',NULL,0,0),(1877,866,'eco_distro','Marine,','Gomont 1899',NULL,0,0),(1878,837,'description','Filaments solitary among other algae, 5.8-6.5 μm wide; sheaths very thin, trichomes blue-green, not constricted at cross-walls.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1879,837,'eco_distro','Aerophytic, described from soil in a wood in Puerto Rico (Coamo).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1880,856,'description','Filaments not forming a stratum, more or less scattered among other algae, 5.8-6.5 um diam.; trichomes not constricted; apices not attenuated; cells quadrate to slightly longer than broad, homogeneous, aeruginous; cross-walls conspicuous; apical cells rounded to blunt-conical; sheath very thin, white, 0.5- 0.8 um diam.; branching single, moderately abundant.','Gardner 1927',NULL,0,0),(1881,856,'eco_distro','Growing on soil in the woods, Coamo Springs, no. 272 b, type','Gardner 1927',NULL,0,0),(1882,838,'description','Thallus tufty, clustered, dark blue-green; filaments densely entangled, 18-21 μm wide, richly pseudobranched; sheaths colourless, homogeneous, 2-2.5 μm thick; trichomes 17-18 μm wide, not constricted at cross-walls, cells shorter than wide to almost isodiametric.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1883,838,'eco_distro','Freshwater, on stones from flowing waters in central Africa (Gabon).','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1884,857,'diagnosis','Stratum caespitosum, lanosum, obscure aerugineum; fila valdre intricata, flexuosa ad tria millimetra longa, 18-21 um crassa, crebre et repetite pseudoramosa; rami solitarii, aut etiam fasciculati, saepius gemini et tune inter se ad basin sat longe coaliti, aut etiam cruciati, filo primario conformes; vaginae hyalinae, homogeneae, laeves, utrinque 2-2,5 um crassae, chlorozincico iodurato haud caerulescentes; trichomata pulchre caerulea, 17-18 um ad genicula haud constricta, apicem versus nec attenuata, nec capitata; articuli saepius subquadrati aut paulo &nbsp;longiores quam latiores, interdum apicem versus ad dimidium breviores, protoplasmate grosse granuloso farcti; dissepimenta non granulata; cellula apicalis superne non attenuata, rotundata.','Frémy 1930',NULL,0,0),(1885,857,'eco_distro','Freshwatre; Gabon, near Mbigou','Frémy 1930',NULL,0,0),(1886,1444,'description','Thallus expanded, pinkish or red-brown, ± thin, membranaceous. Filaments entangled, long, richly and repeatedly pseudobranched; pseudobranches in pairs, distant, long, thinner than main filaments, nearly hair-like towards ends. Sheaths colourless, thick. Trichomes pinkish or reddish, 1-2.2(2.5) μm wide, not or very slightly constricted at the ungranulated cross-walls, not attenuated at the ends. Cells short, up to 1/3 x as long as wide, 0.4-1.5 μm long; cell content homogeneous. Apical cells rounded.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1887,1444,'eco_distro','Marine, on rocks, shells of molluscs, in aquaria and periphytic on algae, widely distributed in Mediterranean Sea (Greece, Italy), known also from Baltic Sea (Sweden); recorded also from N American coasts.','Komárek &amp; Anagnostidis 2005',NULL,0,0),(1888,1445,'diagnosis','Roseum vel rubro-fuscum, stratum expansum in rupibus marinis formans, aut in Algis majoribus insidens. Fila intricata, elongata, flexuosa, abundanter, etiam repetite pseudo-ramosa; pseudo-rami geminati, patentes, elongati, lilo primario tenuiores, subflagelliformes. Vaginae hyalinae, crassiusculae, chlorozincico iodurato vis coerulescentes. Trichomata roseola, brevi-articulata, torulosa, 1 ,2-2 um crassa; articuli diametro usque ad triplo breviores. Protoplasma homogeneum; cellula apicalis rotundata.','Gomont 1899',NULL,0,0),(1889,2221,'description','Macrocolonies in form of thin, blue-green film growing on agar surface. Filaments long, occasionally coiled or slightly waved, seldom containing two trichomes, with or without sheath, 1.8–2 (4.5) μm wide. Mucilaginous sheaths colorless, soft, hyaline to firm and persistent beyond the apex of the trichome, rarely slightly swollen, clearly visible as wider than the trichome, in older stages mostly firm. Trichomes distinctly constricted at the cross-walls, granulated mostly in the older stages, 1.5–2 μm wide. Cells bright blue-green when young, pale green when old, from isodiametric to elongate, 1.5–2.5 (4) μm long, rarely with polar granules. Apical cells rounded to slightly conical, elongated up to 4.5 μm long. Thylakoids peripheral, necridia present.','Shalygin et al. 2020',NULL,0,0),(1890,2222,'description','Filaments long to short, arranged in parallel or spiral, with or without sheaths, 2 μm wide. Sheath firm, colorless, thin, usually visible only during or following hormogonia formation. Trichomes isopolar, unbranched, untapered, clearly constricted near the transverse cell walls, 0.7–1.8 μm wide. Cells isodiametric, blue-green, not granulated, 0.5–1.2 μm long. Apical cells rounded, same size as regular cells. Hormogonia short, 2-8 celled usually with appressed cells. Necridia frequent. Thylakoids parietal.','Shalygin et al. 2020',NULL,0,0),(1891,2222,'other','<strong>Comparison with other taxa:</strong>—Up until this manuscript, Stenomitos contained only three species: <em>S. rutilans</em> Miscoe et J.R. Johansen in Miscoe et al. (2016: 85), <em>S. tremulus</em> (J.R. Johansen et Casamatta in Casamatta et al. 2005: 420) Miscoe et J.R. Johansen in Miscoe et al. (2016: 86), and<em>&nbsp;S. frigidus</em> (Fritsch 1912: 31) Miscoe et J.R. Johansen in Miscoe et al. (2016: 86). <em>Stenomitos kolaensis</em> and <em>S. rutilans</em> are easily distinguished under the microscope via differences in coloration: blue-green versus red-brown, respectively, as well as differences in diameter and length of the cells, and the occurrence of necridia in <em>S. kolaensis</em> (Table 1). It is unlikely that geographical distribution for the <em>S. kolaensis</em> from the near Arctic will overlap with Hawaiian taxa in tropical rainforest climate.<em>&nbsp;S. tremulus</em> was isolated from a pond in Bylot Island, Nunavut, Canada at a latitude very similar to the site in the Kola Peninsula from which <em>S. kolaensis</em> originates. <em>S. kolaensis</em> was isolated from soils, has wider trichomes and shorter cells than<em>&nbsp;S. tremulus</em>, and shares only 97.75% genetic identity based on the 16S rRNA gene; it is consequently easily separated from that species.<br><em>S. hiloensis</em> is ecologically similar to <em>S. rutilans</em>, but shows clear phylogenetic and morphological separation from <em>S. rutilans. S. hiloensis</em> has blue-green cells in contrast to red-brown in <em>S. rutilans</em>, additionally filament were little bit wider. <em>S. hiloensis</em> is thinner and has shorter cells than <em>S. kolaensis</em>.','Shalygin et al. 2020',NULL,0,0),(1892,481,'description','Stenomitos Miscoe et Johansen (2016) emend. Filaments without false branching, less than 2.5 μm wide. Sheaths thin, in some species firm, persistent, and swollen, sometimes containing two or rarely more trichomes. Trichomes short to long, with necridia present or absent, evidently constricted in some species. Cells longer than wide, occasionally isodiametric, with parietal thylakoids. Apical cells cylindrical, rounded, or conical. Polar granules forming in stationary growth phase.','Shalygin et al. 2020',NULL,0,0),(1893,1599,'description','(sub <em>​Chroococcidiopsis cyanosphaera)</em> Cells spherical to oval, solitary or in irregular clusters, with bluish-grey +- homogeneous content, REproduction by up to 64 (and more) endospores, developing by a simultaneous division of the protoplast; the endospores are released by a rupture of the mother cell-wall, but sometimes reach full growth before a futher forming of endospores inside the original sporangia. Endospores spherical, 2-3um in diameter; vegetative cells up to 20(30) um in diameter; sporangia (with differentiating protoplast) up to 30(40) um in diameter.','Komárek &amp; Hindák 1975',NULL,0,0),(1894,2225,'diagnosis','Akin to <em>Nodosilinea nodulosa</em>, distinguished from it by pseudobranched filaments and its occurrence on wetted sand. Different from any other representatives of the genus <em>Nodosilinea </em>by its phylogenetic position based on 16S rRNA and 16S-23S ITS rRNA gene phylogenies, p-distance analysis, and differences in secondary structures of Box-B helices.','Davydov et al. 2020',NULL,0,0),(1895,2225,'description','In liquid medium form macroscopic, blue-green loose aggregates floating on the surface or settle to the bottom of the glass. In agar plate strain forms a tight blue-green mat. In natural populations filaments are quite long, occasionally slightly waved, mostly unbranched, rarely with single pseudobranchings. Nodules present—up to 4 μm wide in low light in the culture only. Sheaths soft, thin, colorless, adherent to the edges of the cells, sometimes widened, hyaline. Trichomes are distinct constricted at the cross walls, with cells dividing throughout the trichome length. Cells in natural populations are elongate, in cultures shorter to longer than wide 1.2–2.1 μm long (on the ends of trichomes longer than in the middle parts), 1.2–1.7 μm wide, blue-green, pale blue-green when old, often with one prominent granule per cell. At the end of trichomes cells are rounded, similar to intercalary cells. Hormogonia and necridic cells are (rare) presented.','Davydov et al. 2020',NULL,0,0),(1896,529,'description','The thallus morphology ranges from tufts to extensive mats. The coloration is highly varied, ranging from dark red to greenish-brown. Filaments 30–67 (-82) μm in width. Sheaths are colourless, thin (1–2 μm, but can be 12 μm wide in extreme situations), slightly lamellose. Trichomes are cylindrical, attenuated at the ends, constricted on the cell walls, cells (25) 30–65 (70) μm wide and 3–7 μm long. Apical cells are rounded, without calyptra. The genomic DNA G+C content is 41.2 mol%.&nbsp;','Tronholm &amp; Engene 2019',NULL,0,0),(1897,528,'description','Large filamentous cyanobacteria are common in tropical marine oceans, abundant on coral reefs, rocks or mangroves at depths ranging between 0.3–30 m. Filaments are unbranched, &lt;10 cm in length, with wide diameters [25–65 (82) μm]. Trichomes are cylindrical, not attenuated towards ends, constricted or not constricted on crosswalls, surrounded by thick (3–5 μm) and distinct polysaccharide sheaths. The sheaths are typically covered by a rich diversity of mucus (often containing heterotrophic bacteria and other micro-organisms). The cells are discoid, always shorter than they are wide [20–55 (70) μm wide and (2) 3–10 μm long]. The trichomes contain necridic cells separating the trichomes into hormogonia. The terminal cells of the filaments and those of the hormogonia are rounded. Non-diazotrophic and the filaments lack heterocysts or other specialized cells. Members of the genus are photosynthetic and contain phycobiliproteins (phycocyanin, phycoerythrin, and allophycocyanin) and chlorophyll a. Strains are often rich in bioactive secondary metabolites typically biosynthesized by PKS, NRPS or mixed PKS/NRPS pathways.','Tronholm et Engene 2019',NULL,0,0),(1898,602,'diagnosis','In culture, macroscopic benthic mats were observed at the beginning of cultivation, followed by the formation of a fine green layer on the surface of the liquid culture medium. There were straight and coiled trichomes (without sheath), solitary or enclosed by diffluent mucilage. Trichomes are uniseriate, isopolar, short (120 μm long), non-branched with both intercalary (rare) and terminal (very frequent) heterocytes. Terminal heterocytes were observed at both ends after a symmetrical division of a single, elongated and intercalary vegetative cell, while akinetes are formed at the paraheterocytic position. Unipored intercalar heterocytes were also detected in the trichomes. Vegetative cells are constricted, quadratic or longer than they are wide (3.5–6.9 μm length and 3.7–4.5 μm width) and contain aerotopes (completely or partially absent or/and present throughout the &nbsp;trichomes). Heterocytes are usually spherical or sub-spherical, intercalary (bipored and rare) and terminal at both ends (unipored and frequent) with lengths of 3.6–6.3 μm and widths of 3.6–4.8 μm. Akinetes are oval or cylindrical, developing paraheterocytic (slightly distant from heterocytes by 4 vegetative cells), solitary or in rows, with lengths of 7.0–10.6 μm and widths of 5.0–8.0 μm. Mature akinetes are frequently found detached from trichomes.','Genuário et al. 2018',NULL,0,0),(1899,2226,'diagnosis','Differs from the type species, <em>O. subterranea</em>, by the blue-green colour. Differs from all other species in having granules at the crosswalls.','Osorio-Santos et al. 2014',NULL,0,0),(1900,2226,'description','Thallus a thin spreading mat, with aggregations of filaments forming wavy extensions from the central mass, not penetrating the agar, bright blue-green. Filaments flexuous, rarely false branched, with sheath 1.3–1.7 μm wide. Sheath absent, or thin and tightly attached or distinctly widened, colourless, 0.5–1 μm thick. Trichomes motile, with a pair of minute granules frequently flanking the crosswalls, with occasional elongated granules, sometimes with only very minute granules flanking the crosswalls, unconstricted to slightly constricted at the crosswalls, lacking false branching, lacking necridia, with breakage occurring following oblique cross-wall formation, untapered, 0.8–1.3–(1.7) μm wide. Cells consistently longer than wide, with non-granular cytoplasm, with parietal thylakoids sometimes evident in the light microscope, (1.4)–1.6–6.6–(8.7) μm long. Apical cells when mature bluntly conical, on average slightly longer than vegetative cells, with a reddish-orange spot in the apex of the cell, 2.1–7.7–(12.8) μm long. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a bilateral bulge at nucleotides 16-17/41-42, and the subterminal bilateral bulge at nucleotides 22-24/34-36, similar in structure to the type species. V2 helix 17 nucleotides long with a terminal loop of only 3 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix with a large bilateral bulge (6 nucleotides) in mid helix.','Osorio-Santos et al. 2014',NULL,0,0),(1901,480,'description','Thallus a thin mat, spreading evenly and diffusely from the centre of the thallus, penetrating into the agar, intense blue-green. Filaments flexuous, sometimes coiled, with sheath common but not obligately formed, with sheath 1.2–1.7 μm wide. Trichomes motile, unconstricted to slightly constricted at the crosswalls, lacking false branching, lacking necridia, with breakage occurring following oblique crosswall formation, untapered, 0.9–1.4 μm wide. Cells consistently longer than wide, with nongranular cytoplasm, with parietal thylakoids sometimes evident in the light microscope, 1.0–4.4 μmlong. Apical cells when mature bluntly conical, on average longer than vegetative cells, with a reddish-orange spot in the apex of the cell, 1.3–7.8 μm long, 0.9–1.5 μm wide. D1-D1′ helix of the 16S-23S ITS region 124 nucleotides long, with a short side helix on the 3′ side of the helix. V2 helix with 51 nucleotides, with three bilateral bulges. Box-B with 32 nucleotides, with 4 nucleotides in the terminal loop. V3 helix not differing in structure from the type species.','Osorio-Santos et al. 2014',NULL,0,0),(1902,480,'diagnosis','Differs from all other species in the length and structure of the D1-D1′ helix of the 16S-23S ITS region.','Osorio-Santos et al. 2014',NULL,0,0),(1903,2227,'description','Thallus a thin mat, with some aggregations of filaments extending from the central mass, not penetrating into the agar, blue-green. Filaments flexuous, rarely with more than one trichome in common mucilage, with sheath 1.4–2.4 μm wide. Sheath very common, nearly obligate in older cultures. Trichomes motile, unconstricted to slightly constricted at the crosswalls, often with minute granules flanking the crosswalls, lacking false branching, lacking necridia, with breakage occurring following oblique crosswall formation, untapered, 1.1–1.9 μm wide. Cells consistently longer than wide, with nongranular cytoplasm, with parietal thylakoids sometimes evident in the light microscope, 1.0–4.4 μm long. Apical cells when mature bluntly conical, on average longer than vegetative cells, with a reddish-orange spot in the apex of the cell, 2.0–5.8 μm long, 1.0–1.7 μm wide. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix 15 nucleotides long, with a large terminal loop of 9 nucleotides. Box-B with 34 nucleotides, with 5 nucleotides in the terminal loop. V3 helix region with 52 nucleotides, with a unilateral bulge on the 5ʹ side of the helix at nucleotides 9-12.','Osorio-Santos et al. 2014',NULL,0,0),(1904,2227,'diagnosis','Morphologically most similar to <em>O. neakameniensis</em>, from which it differs in the higher degree of sheath formation and shorterminimum cell length, also differing fromthat taxon and all others in the length and structure of the V2 helix of the 16S-23S ITS.','Osorio-Santos et al. 2014',NULL,0,0),(1905,2227,'etymology','<em>hafneriensis </em>= from Hafnersee','Osorio-Santos et al. 2014',NULL,0,0),(1906,2228,'diagnosis','Morphologically most similar to <em>O. hafneriensis</em>, differing from that taxon by length and structure of the V2 helix of the 16S-23S ITS region. Also similar to the desert soil species <em>O. coburnii, O. mojaviensis</em> and<em> O. atacamensis</em>, but differing from all those species by having thinner trichomes and a unique secondary structure in the V3 helix of the 16S-23S ITS region.','Osorio-Santos et al. 2014',NULL,0,0),(1907,2228,'description','Thallus a thin mat, spreading evenly and diffusely from the centre of the thallus, not penetrating into the agar, blue-green. Filaments flexuous, with sheath frequently present, nearly obligate in older cultures, with sheath 1.2–4.1 μm wide. Trichomes motile only in newly transferred cultures, sometimes with minute granules flanking the crosswalls, unconstricted to slightly constricted at the crosswalls, lacking false branching, lacking necridia, with breakage occurring following oblique crosswall formation, untapered, 1.2–1.7 μm wide. Cells consistently longer than wide, with nongranular cytoplasm, with parietal thylakoids sometimes evident in the light microscope, 1.5–5.4 μm long. Apical cells when mature bluntly conical, on average longer than vegetative cells, with a reddish-orange spot in the apex of the cell, 2.3–7.7 μm long, 1.1–1.7 μm wide. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix with<br>only 8 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix region with<br>52 nucleotides, with a bilateral bulge at nucleotides 12-14/43.','Osorio-Santos et al. 2014',NULL,0,0),(1908,2228,'etymology','<em>neakameniensis</em> = from the island Nea Kameni','Osorio-Santos et al. 2014',NULL,0,0),(1909,2229,'diagnosis','Morphologically and ecologically most similar to <em>O. neakameniensis</em>,<em>&nbsp;O. coburnii</em> and <em>O. atacamensis</em>, differing from these species in the production of necridic cells.','Osorio-Santos et al. 2014',NULL,0,0),(1910,2229,'description','Thallus a thin mat, spreading unevenly but diffusely from the centre of the thallus, penetrating into the agar, blue-green. Filaments flexuous, with sheath common, especially in older cultures, rarely false branching, with sheath 2.0–2.6 μm wide. Trichomes motile only in newly transferred cultures, with minute granules rarely at the crosswalls, unconstricted or slightly constricted at the cross-walls, with breakage occurring following formation of necridic cells or rare oblique cross-wall formation, untapered, 1.6–2.2 μm wide. Cells isodiametric or mostly longer than wide, with nongranular cytoplasm, with parietal thylakoids evident in the light microscope, 1.5–5.0 μm long. Apical cells when mature bluntly conical, on average longer than vegetative cells, rarely with irregular outgrowth, with a reddish-orange spot in the apex of the cell, 2.4–6.8 μm long, 1.4–2.0 μm wide. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix with only 8 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix region with 52 nucleotides, with a unilateral bulge on the 5′ side of the helix at nucleotides 9–12.','Osorio-Santos et al. 2014',NULL,0,0),(1911,2230,'diagnosis','Morphologically and ecologically most similar to <em>O. neakameniensis, O. mojaviensis</em> and<em> O. atacamensis</em>, differing from these taxa in structure in the terminal loop of the Box-B helix of the 16S-23S ITS region.','Osorio-Santos et al. 2014',NULL,0,0),(1912,2230,'description','Thallus a thin mat, spreading unevenly but diffusely from the centre of the thallus, not penetrating into the agar, blue-green. Filaments flexuous, with sheath rare, rarely false branching, with sheath 1.7–2.8 μm wide. Trichomes motile only in newly transferred cultures, without granules at the cross-walls, slightly to distinctly constricted at the crosswalls, lacking necridia, with breakage occurring following rare oblique cross-wall formation, untapered, 1.4–1.8 μm wide. Cells isodiametric to longer than wide, with nongranular cytoplasm, with parietal thylakoids sometimes evident in the light microscope, 1.8–4.8 μm long. Apical cells when mature bluntly conical, on average longer than vegetative cells, rarely with irregular outgrowth, with a reddish-orange spot in the apex of the cell, 2.4–5.4 μm long, 1.4–1.8 μm wide. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix with only 8 nucleotides. Box-B with 34 nucleotides, with 4 nucleotides in the terminal loop. V3 helix region with 52 nucleotides, with a unilateral bulge on the 5′ side of the helix at nucleotides 9–12.','Osorio-Santos et al. 2014',NULL,0,0),(1913,2230,'etymology','<em>coburnii </em>= named in honour of Professor Miles C. Coburn','Osorio-Santos et al. 2014',NULL,0,0),(1914,2231,'diagnosis','Similar to the arid soil species <em>O. coburnii, O. mojaviensis</em> and <em>O. neakameniensis</em>, but differing from those species by having a unique secondary structure in the V3 helix of the 16S-23S ITS region.','Osorio-Santos et al. 2014',NULL,0,0),(1915,2231,'description','Thallus a thin mat, spreading unevenly but diffusely from the centre of the thallus, penetrating into the agar, blue-green. Filaments flexuous, rarely with more than one trichome in a common mucilage, with sheath common, especially in older cultures, rarely false branching, with sheath 1.8–4.1 μm wide. Trichomes not motile, with minute granules rarely at the crosswalls, slightly constricted at the crosswalls, with breakage occurring following oblique crosswall formation, untapered, 1.5–2.3 μm wide. Cells isodiametric or mostly longer than wide, with nongranular cytoplasm, with distinct parietal thylakoids in the light microscope, 1.5–7.4 μm long. Apical cells when mature bluntly conical, on average longer than vegetative cells, rarely with irregular outgrowth, with a reddish-orange spot in the apex of the cell, 2.5–9.9 μm long, 1.4–2.1 μm wide. D1-D1′ helix of the 16S-23S ITS region 64 nucleotides long, with a large subterminal bilateral bulge of 9 nucleotides. V2 helix with only 8 nucleotides. Box-B with 34 nucleotides, with 6 nucleotides in the terminal loop. V3 helix region with 52 nucleotides, with minor mismatches in the helix at nucleotides 9/49, 12 and 15–16.','Osorio-Santos et al. 2014',NULL,0,0),(1916,2232,'description','Filaments solitary or forming loose fascicles, straight or flexuous, enveloped by thin, hyaline, and colorless sheaths. Trichomes isopolar, cylindrical, straight or curved, blue-green, not or slightly constricted at the cross–walls, not attenuated, 3.24–4.25 μm wide. Single trichomes have firm, colorless, unlamellated sheaths, open at the end. Vegetative cells isodiametric or rarely longer or shorter than wide, 2.61–5.35 μm long, with scattered large granules. Terminal cells rounded or conical, without calyptra. Thylakoids parietal, fasciculated. Reproduction by disintegration of the trichomes without necridic cells.','Lee et al. 2020',NULL,0,0),(1917,2233,'description','Natural samples are macroscopic green colonies in wet soil or seepage, almost 2–3 mm in diameter and convex hemispherical, have a thick and rough texture with slimy exterior, and have slightly curved filaments with true branching. In the laboratory-grown culture, apical cells are curved at the ends but are not always rounded; filament length varies from short to long; vegetative cells also vary from square to barrel-shaped, sometimes slightly cylindrical or spherical; vegetative cells appear constricted prominently. Terminal vegetative cells range in length from 3.41 to 5.68 μm and in width from 2.53 to 3.61 μm, intercalary vegetative cells are 2.80 to 5.63 μm in length and 2.80 to 4.39 μm in width. Slightly colourless mucilaginous texture is present all around the trichomes. Heterocytes are prominent, spherical to globose in shape, appear at both the terminal and the intercalary positions, and are light green to yellowish. Terminal heterocytes are 4.69–5.94 μm in length and 3.24–3.56 μm in width, while intercalary heterocytes are 5.22–6.74 μm in length and 5.35–6.53 μm in width.','Singh et al. 2020',NULL,0,0),(1918,2234,'description','Bluish-green mat growing luxuriantly in soil constantly seeped by water from adjoining freshwater lake. Laboratory-grown culture shows creeping growth on solid media. Filaments usually isopolar, rarely heteropolar, when isopolar having broadened terminal ends and narrow middle part, when heteropolar broadening observed only at the apical end. Sheath thin, mucilaginous and present throughout the length of the trichome. Trichome prominently constricted at the crosswalls in the broadened part and slightly constricted in the narrow part. Vegetative cells shorter than wide at the broadened ends, longer than wide in the narrow middle part; barrel shaped at the broadened ends, 3.6–5.0 μm long, 4.9–5.8 μm wide; cylindrical to elongated in the middle part, 7.5–9.5 μm long, 3.7–4.9 μm wide. Heterocytes terminal and intercalary with or without vacuoles. Terminal heterocytes rare, oblong, 6.0–7.0 μm long, 5.5–6.0 μm wide. Intercalary heterocytes abundant and variably shaped; when oblong compressed 5.0–6.7 μm long, 6.0–7.3 μm wide; when oblong 6.9–8.3 μm long, 6.4–7.7 μm wide; when oblong elongated 10.8–15.3 μm long, 5.0–6.8 μm wide. Hormogonia present; tapered; with terminal heterocyte. Monocytes released from the broadened end of the filaments. Akinetes observed; circular; 10.0 μm in diameter. Necridia bow-shaped.','Saraf et al. 2020',NULL,0,0),(1919,2235,'description','Populations of Cyanocohniella crotaloides sp. nov. show a polymorphic life cycle. The adult and main form resembles those of Nostoc-like thallus structures with curved, constricted filaments that are embedded in a nonlamellated, fine and colorless sheath. The cells are round to spherical, 2.1–3.7 μm in diameter, with parietal thylakoids, and rarely with intercalary oval to spherical heterocyts. Young filaments or motile hormogonia show a Pseudanabaena/Leptolyngbya-like morphology with constricted cells that are cylindrical and 1.5–3.1 μm wide. The apical cells of these filaments are longer than wide, 1.5–3.1 μm, and oval to conical. Mature filaments resemble a Chlorogloeopsis-like morphology with cells of different sizes in one trichome formed by cell division in two planes. The cells are spherical, oval, or irregularly shaped and vary from 2.6 to 5 μm. The filaments are ensheathed in a visible, firm, and colorless sheath with apical and multiple intercalary hormocytes. Akinetes are formed in this stage and stayed attached to the filaments as single cells or in series with a brownish color. The cells are spherical to oval, 2.8–6.3 μm in diameter. The species tested negatively for nodularin/microcystin genes.','Jung et al. 2020',NULL,0,0),(1920,2235,'etymology','‘Crotaloides’ according to the rattlesnake-like habit of the Chloreogloeoposis-like stage where variable cell types and cell sizes are combined and look like a rattle.','Jung et al. 2020',NULL,0,0),(1921,2236,'description','The species has single filaments without false branching that are 0.8–1.6 μm wide with a firm sheath. The trichomes and single cells are 0.5–1.1 μm wide (0.7 μm in average)/1.2–2.9 μm long, frequently granulated, and constricted at the cross walls with a parietal organization of the thylakoids. Apical cells are longer than broad, 0.6–2.5 μm wide/1.5–7.7(9.5) μm long with the typical orange ‘eye-spot’ in the very tip of the apical cells of mature filaments. The species tested positively for nodularin/microcystin genes.','Jung et al. 2020',NULL,0,0),(1922,2237,'description','Microscopic irregular or rounded colonies with variable number of cells (up to 32–64 cells or more), usually aggregated into irregular, extended, compact multicolonial groups, sometimes solitary cells. Mucilage unstratified, colorless, and firm surrounding cells and colonies. Cells mostly irregular to rounded, 1.5–3.2 um long, 1.5–2.4 um in diameter with parietal thylakoids. Cell contents blue-green, slightly granulated, or sometimes homogeneous. Thylakoids parietal. Reproduction by simple binary cell division in three or more planes. The species tested negatively for nodularin/microcystin genes.','Jung et al. 2020',NULL,0,0),(1923,2238,'description','Dark greenish brittle and soft mat like growth in the shade of herbaceous plants. The lab grown culture shows star like diffused growth on agar plates. The filaments are profusely branched with typical unidirectional/bidirectional T-type branching. The prostrate filaments give rise to erect lateral branches with very slight tapering at the branch ends. The young filaments aremonoseriate but the older prostrate filaments may also show biseriate condition. Cells of the prostrate filaments are distinctly constricted while the cells of the lateral branch lack them. The vegetative cells adjacent to heterocytes appear oblong with compressed ends, and range in size from7.1–9.3 μm in length to 3.5–4.7 μm in width. The vegetative cells away from heterocytes are irregular in shape and can be spherical or even elongated with size ranging from 3.6–7.2 μm in length to 3.5–6.1 μm in width. Heterocytes in prostrate filaments are differently shaped and can be spherical to oblong to elongated and range in size from 3.7–9.3 μm in length to 2.5–6.7 μm in width. Monocytes range in size from5.6–6.2 μmin length to 3.5–3.8 μm in width and appear oval or oblong, slightly compressed in the middle and are liberated from prostrate filaments. Akinetes are characteristically thick walled and granulated and larger than cells of the prostrate filament. Akinetes range in size from 6.5–7.8 μm in length to 3.4–4.5 μm in width. The heterocytes near to the chain of akinetes appear irregularly shaped, highly granulated and cylindrical with distinct polar granules. All the cells have slight colorless sheath surrounding them.','Mishra et al. 2020',NULL,0,0),(1924,2250,'diagnosis','Strato epilithico, crustaceo, cum aliis algis permixto. Filamentis e centro radiantibus vel inordinate inter alias algas permixtis, ad 500 um longis, im superiore parte usque ad 35 um crassis, pseudoramosis. Trichomatibus, praesertim apud exemplaria adulta, basim versus eximie attenuatis, apice 2—3,5 crassioribus quam media parte; aerugineis, sub apice tantum ad genicula constrictis. Cellulis 2 um (ad basim) usque ad 8 um (sub apice) crassis; in superiore parte dimidio et ultra crassioribus. Vaginis crassissimis, dilute luteobrunneolis, stratosis vel homogeneis, saepe diffluentibus. Heterocystis singulis, basalibus, 6—9 um crassis.','Ercegović 1925',NULL,0,0),(1925,2251,'description','Stratum obscure-viride. Trichomata pallidissime aeruginosa, ad genicula constricta, apicibus conicis. Vagina tenuissima, distincte observata. Cellulae quadratae vel cylindraceae, disjunctae, protoplasmate homogeneo vel minute granulato. Heterocystides rotundato-conicae vel oblongae subcylindraceae; apicibus rotundatis. Gonidia stricte cylindracea, lateritibus planis, apicibus truncatis; vel doliformia, lateribus levissime arcuatis, apicibus truncatis; vel rarius elliptico-lanceolata, apicibus rotundatis;protoplasmate granulato, dilutissime aeruginoso paene hyalino. Trich. diam. 4-5; cell. alt. 6-10, saepe 8 um. Heterocyst. conic, long. 6-10, lat. 5-6, cylindr. long. 11-12, lat. 6 um. Gonid. cylindr. long. 12-15, lat. 5-6, doliform. long. 1 6-20, lat. 7-8, lanceol. 22 x 10um.','Playfair 1915',NULL,0,0),(1926,920,'description','-','Kaštovský et al. 2014',NULL,0,1),(1927,709,'description','','Kaštovský et al. 2014',NULL,0,1),(1928,920,'description','Population with a polymorphic life cycle. Hormogonia and young filaments with isodiametric to cylindrical cells, not constricted or slightly constricted at cross-walls, (1)1.5(2) μm wide, with intercalary cells (1)1.5–2.5 μm long, with apical cells longer than wide, oval to conical, 1.5–2.5 μm long. Sheath absent or thin, fine, colorless to slightly yellow (Figs. 1A–C). Intercalary cells gradually become constricted at the cross-walls and oval to spherical shape, (2)3.0–4.5(5) μm in diameter. Intercalary heterocytes rarely present, oval or spherical, 5–6(7) μm in diameter. Apical cells remain similar in form to intercalary cells, but may become less wide as filaments become attenuated towards apices (Figs. 1D–H). Mature filaments with cells spherical, oval or irregularly shaped, 2–7(8) μm in diameter, with cells irregularly arranged in ensheathed filaments, sometimes evidencing cell division in two planes, partly biseriate, with heterocytes rarely present, sheath colorless to slightly yellow, usually thin, unlamellated (Figs. 1K–N). Akinetes single or in series, spherical to oval, often with yellowish cell walls, 4–8(10) μm in diameter.','Kaštovský et al. 2014',NULL,0,0),(1929,709,'other','Thallus blue-green to dark green, filaments hypervariable in the course of the life cycle. Motile hormogonia germinating from akinetes, composed of 4–8 cells. Filaments developing from hormogonia with cylindrical cells, not constricted or slightly constricted at cross-walls, without sheath or with fine colorless or slightly yellowish, unlamellated sheath, slightly attenuated towards apices, with apical cells longer than wide, oval to conical, lacking calyptra. Filaments of next phase with marked constrictions at the cell walls, attenuated towards apices, with cells becoming oval to spherical, producing intercalary oval to spherical heterocytes and one- to two-celled apical hormocytes, with apical cells similar in form to common cells of the filament. Filament of mature phase with cells spherical, oval or irregularly shaped, with cells irregularly arranged in ensheathed filaments, sometimes evidencing cell division in two planes, producing partly biseriate filaments. Akinetes single or in series, with cell walls often yellowish. Necridia absent during entire life cycle.','Kaštovský et al. 2014',NULL,0,0),(1930,2252,'description','Thallus light to dark blue green, coiled, epipelic on sand/mud, embedded in clear gelatinous matrix, pseudofilaments ± 1 mm long, curved and wavy, 24.0–29.2 (30) μm diam. Unicellular pseudofilaments, mostly uniseriate, sometimes pseudopolyseriate, often pseudodichotomously divaricated. Sheath hyaline, gelatinous, 2.6 μm thick, bacterial film often embedded. Healthy, dividing cells and divaricating pseudofilaments contain little to no space between cells. Slight or clear distance between cells in older pseudofilaments. Cell content light to dark green to blue–green, very finely granular, homogeneous, without gas vesicles. Cells discoid, 4.0–7.8 (8.8) μm long and 18.5–23.3 (23.7) μm in width. Apical cell rounded, light green to yellow. Reproduction through filament disintegration, necridia. Forms club–shaped, expansion of cells (8–12 cells) that are twice wider than vegetative cells.','Berthold et al. 2020',NULL,0,0),(1931,2252,'diagnosis','Cells of pseudofilaments are much larger than previous species including <em>Johannesbaptistia pellucida</em>,<em> J. primaria</em>, and<em> J. willei</em>.','Berthold et al. 2020',NULL,0,0),(1932,2253,'description','Thallus a thin mat, Filaments flexuous, lacking false branching, sometimes more than one trichome in a common sheath, 1.2–8 μm wide. Sheath firm, thin, colorless, becoming widened, lamellate, with wavy edges, up to 4 μm wide. Trichomes not motile, constricted at the crosswalls, 1–1.8 μm wide. Cells non–granular, blue–green, longer than wide, 2.1–4.4 μm long. Apical cells conically tapered when mature, with a prominent red granule at the tip of the cell, 4.4–5.0 μm long.','Becerra-Absalón et al. 2020',NULL,0,0),(1933,2253,'diagnosis','Morphologically similar to <em>O. kazantipica</em> by the presence of widened, lamellate sheath, but <em>O. dilatativagina</em> differs in constrictions or very marked wavy edges in the sheath, also false branches were not observed, the cells are shorter, have no granules, and are from a different habitat. Ecologically similar to <em>O. leona</em>, <em>O. mojaviensis</em>, <em>O. coburnii</em>, <em>O. atacamensis</em> and<em> O. neakameniensis</em>, but morphologically differing from these species by the very widened sheath and by the maximum width of the filament.','Becerra-Absalón et al. 2020',NULL,0,0),(1934,2254,'diagnosis','Morphologically and ecologically similar to<em> O. mojaviensis</em>, <em>O. atacamensis</em> and <em>O. coburnii</em>, but differing by slightly thicker filaments and absence of false branching.','Becerra-Absalón et al. 2020',NULL,0,0),(1935,2254,'description','Thallus a thin mat. Filaments flexuous, with a single trichome per sheath, lacking false branches, 2.9–4.4 μm wide. Sheath firm, thin, unlamellated, colorless. Trichomes not motile, not to slightly constricted at the crosswalls, 1.5–2.7 μm wide. Cells non–granular, blue–green, longer than wide, 2.4–4.4 μm long. Apical cells conically tapered when mature, with a prominent red granule at the tip of the cell, 4.0–4.9 μm long. Hormogonia observed, separated by simple fission without necridia.','Becerra-Absalón et al. 2020',NULL,0,0),(1936,2255,'description','Trichomes solitary, almost straight with conspicuous constrictions at cross-walls, brownish green or greenish gray to gray, 1.4–2.5 μm wide, without mucilage or sheath, not attenuated nor differentiated at the ends, without calyptra, not motile. Cells cylindrical, greenish gray to gray, longer than wide, rarely isodiametric, 2.3–9.9 μm long, ratio of width to length 1.1–6.3, with aerotopes at both ends of cells, sometimes with one to several small granules, differentiated in centro- and chromatoplasmic regions. Cell division perpendicular to the longitudinal axis of the trichome. Trichomes separate between two neighboring cells or by fragmentation without necridic cells. Heterocytes are not known. The thallus has the musty odor imparted by 2-methylisoborneol.','Tuji &amp; Niiyama 2018',NULL,0,0),(1937,2256,'description','Trichomes solitary or aggregated to form thin membranous colony, straight or curved with conspicuous constrictions at cross-walls, bright blue-green, 1.5–2.3 μm wide, occasionally with sheath, not attenuated nor differentiated at the ends, without calyptra, not motile, but short trichomes sometimes show trembling. Cells cylindrical with rounded ends, longer than wide or almost isodiametric, bright bluegreen, 1.9–6.8 μm long, ratio of width to length 0.9–4.5, with aerotopes at both ends of cells, differentiated in centro- and chromatoplasmic regions, without granules. Cell division perpendicular to the longitudinal axis of the trichome. Trichomes separate between two neighboring cells or by fragmentation without necridic cells. Heterocytes are not known. Thallus has the extreme musty odor imparted by 2-methylisoborneol.','Tuji &amp; Niiyama 2018',NULL,0,0),(1938,2257,'diagnosis','Monophyletic group of genera based on 16S rRNA and rpoC1/rbcX phylogenies, sister to the clade containing Microcoleus, Limnoraphis, and Trichodesmium, with filaments (1.5) 5.5–7.8 (10.7) μm wide, possessing conical or strongly acuminate apical cells.','Zimba et al. 2020',NULL,0,0),(1939,2258,'diagnosis','Akin to Laspinema (except for strongly acuminate apical cells) and misidentified ‘Oscillatoria acuminata’ by morphology, differs by burrowing movement and by phylogenetic position (16S rRNA, rpoC1/rbcX phylogenies), more closely related to several uncultured tropical lineages from hypersaline lagoons than to Laspinema sensu stricto.','Zimba et al. 2020',NULL,0,0),(1940,2258,'description','Filaments uniseriate; forming circular, nearly concentric fascicles on the surface of agar or as three-dimensional spheres in the liquid culture medium. Sheaths thin, tightly adherent. Bright green trichomes motile with gliding, rotating, burrowing movement. Apical cells long, attenuated in exponential phase, having numerous cell divisions within apical termini in late exponential cultures. Reproduction by hormogonia. Necridia biconcave.','Zimba et al. 2020',NULL,0,0),(1941,2259,'diagnosis','Morphologically similar to Oxynema, differing by burrowing/boring ability, phylogenetic position, thylakoid arrangement, and 16S rRNA p-distance value.','Zimba et al. 2020',NULL,0,0),(1942,2259,'etymology','Named in honour of Dr Wes Tunnell, founding Centre Director of the Centre for Coastal Studies, Texas A&amp;M University Corpus Christi, and scholar who focused our attention on the Laguna Madre’s unique algal flora.','Zimba et al. 2020',NULL,0,0),(1943,2259,'other','Seven toxins produced: two apratoxins and one each of coibacin, cyanopeptolin, lyngbyabellin, microcystin, and malyngamide classes.','Zimba et al. 2020',NULL,0,0),(1944,2261,'diagnosis','Morphologically similar to <em>Komarekiella</em>, from which it differs by the presence of an inclusion/vesicle in the akinetes and smaller size of heterocytes. It also differs in sequences and in most of the ITS secondary structures of the conserved domains of the 16S-23S ITS region.','Soares et al. 2020',NULL,0,0),(1945,2261,'description','xx','Soares et al. 2020',NULL,0,1),(1946,2260,'description','In nature, thalli microscopic, growing on limestone surfaces. In liquid media, forming thin biofilm layers attached to the walls of the test tube, or forming agglomerated dense aggregates deposited at the bottom of the test tube. Cells blue-green, dark green when mature. Cells spherical to subspherical, forming macroscopic compact dense aggregates, enclosed by a mucilage layer (Figs 24–26, 37–40). Cells in trichomes or sometimes free-living, isodiametric, quadrate, straight or straight to bent (Figs 33, 34). Cells divide in more than one plane, forming multiseriate trichomes (Fig. 26). Heterocytes intercalary and terminal (Figs 32, 33), placed laterally when cells are in compact aggregates. Akinetes spherical to subspherical, developing from vegetative cells in trichomes (Fig. 35), reproducing by equal division forming elongated trichomes surrounded by a thick, firm mucilage layer (Figs 27, 28, 35), or by unequal division forming bigger spherical and encapsulated colonies (Figs 29–31, 36). Akinetes with granular content and with frequent presence of inclusions/vesicles (Figs 29, 30, 34–36, 39). The thylakoid arrangement exhibits a fascicular architecture (Figs 38, 39).','Soares et al. 2020',NULL,0,0),(1947,2260,'diagnosis','Morphologically similar to <em>Komarekiella</em>, from which it differs by the presence of an inclusion/ vesicle in the akinetes and smaller size of heterocytes. It also differs in sequences and in most of the ITS secondary structures of the conserved domains of the 16S-23S ITS region.','Soares et al. 2020',NULL,0,0),(1948,2261,'description','Thallus microscopic, blue-green, later dark green, becoming yellowish when very old (more than 6 months). Cells at first forming thin biofilm layers attached to the walls of the test tubes, later forming compact dense aggregates at the bottom of the test tube. Cells in hormogonia isodiametric, quadrate, sometimes wider than longer (1.8–3.4 μm long, 2.4–4.0 μm wide); hormogonia straight or straight to bent, forming uniseriate filaments up to 4 μm wide. Cells spherical or subspherical when mature, dividing in more than one plane, forming multiseriate filaments up to 15 μm wide, creating compact and aggregated colonies. Akinetes spherical or subspherical (3.7–7.9 μm long, 3.2–6.1 μm wide), slightly larger than vegetative cells (2.8–6.3 μm long, 2.5–5.2 μm wide), with granular content and with frequent presence of a vesicle (1.2–2.6 μm in diameter). Heterocytes spherical when terminal; spherical, subspherical or compressed when intercalary (2.1–3.7 μm in diameter).','Soares et al. 2020',NULL,0,0),(1949,2262,'description','Cells more or less spherical, usually densely and irregularly aggregated, attached to the substratum. Cells pinkish to reddish, 3.18–6.48 μm in diameter. Sheaths distinct, thin, colorless. Cells divided irregularly in two or more different planes. Baeocytes successfully arised, rounded. Thylakoids irregularly arranged.','Konstantinou et al. 2021',NULL,0,0),(1950,2263,'description','Filaments consolidated into fascicles, partly rope-like contorted, rarely solitary, unbranched. Filaments forming compact colony (thallus), attached to the substratum, pinkish. Sheaths thin, colorless and slightly to rarely distinct. Trichomes straight to curved, 0.72–1.09 μm wide, slightly constricted at the cross walls. Cells more or less isodiametric, with peripheral thylakoids. Apical cells rounded without calyptra.','Konstantinou et al. 2021',NULL,0,0),(1951,2264,'description','Thallus pinkish, composed of fasciculated filaments (rarely solitary filaments) attached to the substratum. Filaments long with a single trichome per sheath, unbranched, straight to curved. Sheaths colorless, thin, and slightly distinct. Trichomes slightly constricted at the cross walls. Hormogonia rare. Cells longer than wide to isodiametric, 0.89–1.96 μm in length and 0.72–1.09 μm in width. Thylakoids (two to three) arranged peripherally. End cells rounded.','Konstantinou et al. 2021',NULL,0,0),(1952,2265,'description','Filaments joined to densely-arranged irregular clusters, colonies often forming mats on a substratum, straight, curved, more or less coiled. Sheaths firm, thin, colorless, lamellated, containing one to few trichomes. Trichomes cylindrical, 1.3–2.5 μm wide, slightly constricted at the cross walls, attenuated or not towards ends, pinkish to reddish or brownish. False branching and nodule formation are occasionally present. Cells isodiametric, slightly shorter than wide with peripheral thylakoids. Apical cells rounded without calyptra.','Konstantinou et al. 2021',NULL,0,0),(1953,2263,'etymology','From Greek word stem ρoδο- (rhodo-) indicating the rose color and the verb πλέκω (pleko) - intertwine.','Konstantinou et al. 2021',NULL,0,0),(1954,2265,'etymology','The name comes from the Greek Κυματολήγη (Cymatolege) one of the 50 Nereids, daughters of Nereus, sea nymphs of Greek mythology; Cymatolege had the power to stop the waves of the sea.','Konstantinou et al. 2021',NULL,0,0),(1955,2266,'description','Filaments irregularly joined in clusters, straight to curved, tightly spirally coiled, frequently false branched, sometimes forming nodules. Sheaths firm, thin, colorless, containing one to four trichomes. Trichomes pinkish (old trichomes olivish to greyish), slightly constricted at the cross-walls, frequently with loose to tight screw-like coils, attenuated towards ends. Cells more or less isodiametric or slightly shorter (0.76–1.54 μm) than wide (1.06–1.92 μm). Thylakoids (six to eight) arranged peripherally. End cells rounded.','Konstantinou et al. 2021',NULL,0,0),(1956,2267,'description','Filaments long, irregularly joined in clusters, straight, curved or wavy, occasionally false branched. Sheaths firm, thin, colorless, containing one and rarely two or three trichomes. Trichomes not attenuated towards ends. Cells more or less isodiametric, 2.19–1.00 μm in length and 0.92–1.94 μm in width. Thylakoids (five to six) arranged peripherally. End cells rounded.','Konstantinou et al. 2021',NULL,0,0),(1957,2268,'description','Filaments arranged into fascicles, rarely solitary, unbranched. Filaments forming compact colony (thallus), attached to the substratum, purple to reddish. Sheaths thin, colorless and slightly to rarely distinct. Trichomes straight to curved or wavy, 0.57 – 1.76 μm wide, clearly constricted at the cross walls. Cells longer than wide, with peripheral thylakoids. Apical cells rounded (with/without calyptra?).','Konstantinou et al. 2021',NULL,0,0),(1958,2268,'etymology','The name comes from Greek Мῆτις (Metis), a Titaness in ancient Greek mythology, daughter of Oceanus and Tethys, first wife of Zeus.','Konstantinou et al. 2021',NULL,0,0),(1959,2269,'description','Thallus violet to purple, filaments joined in fascicles, rarely solitary, attached to the substratum. Filaments long with a single trichome per sheath, unbranched, straight, curved, or wavy. Sheaths colorless, thin, and slightly distinct. Trichomes clearly constricted at the cross walls. Hormogonia formation present. Cells longer (1.3–2.89 μm) than wide (0.57–1.76 μm). Thylakoids (four to five) arranged peripherally. End cells rounded with a calyptra (?).','Konstantinou et al. 2021',NULL,0,0),(1960,2270,'description','Cells solitary or grouped in irregular clusters, but not forming mucilaginous colonies. Mucilage fine, colorless, around single cells. Cells cylindrical, usually longer (1.17–4.42) than wide (0.61–1.3 μm), with parietal thylakoids. Color of cells is pinkish to pale orange. Reproduction by binary fission.','Konstantinou et al. 2021',NULL,0,0),(1961,2271,'description','Cells solitary or irregularly grouped in clusters. Cells cylindrical with rounded ends, usually three times longer (1.17–4.42 μm) than wide (0.6–1.3 μm), with thin slightly distinct or indistinct mucilage layer. Cells with homogenous or finely granulated content, mostly pinkish.','Konstantinou et al. 2021',NULL,0,0),(1962,2272,'description','Cells solitary or irregularly grouped in clusters. Cells cylindrical with rounded ends, usually two times longer (1.77–3.48 μm) than wide (0.8–1.2 μm), with thin slightly distinct or indistinct mucilage layer. Cells with homogenous or finely granulated content, orange.','Konstantinou et al. 2021',NULL,0,0);
INSERT INTO `cyanodb_data` VALUES (1963,2273,'description','Trichomes usually in fine mats, more or less straight, cylindrical, short, consisting of few to several cells, with conspicuous constrictions at cross walls, without sheaths. Apical cells usually not differentiated, without calyptra (?). Sometime slow gliding motility occurs. Cells cylindrical, rarely barrel-shaped, longer than wide, with or without gas vehicles. Thylakoids arranged peripherally, parallelly to cell walls; the structural (peptidoglycan) layer of the cross-wall is usually thicker than the layer surrounding the rest of the cell; with multiple pores near cells poles.','Konstantinou et al. 2021',NULL,0,0),(1964,2273,'etymology','The genus name is made of the Greek word θαλασσοπόρος (thalassoporos) [from θάλασσα (thalassa) - sea and πορεία (poreia) - course, route], meaning the seafarer, the navigator.','Konstantinou et al. 2021',NULL,0,0),(1965,2274,'description','Trichomes rarely solitary, usually in fine, thin, indefinite, prostrate colonies (fine mats), forming brownish-red clusters. Trichomes straight, rarely curved, few celled (3–10), deeply constricted at cross walls, not attenuated at the ends. Cells cylindrical with rounded ends, longer (1.3–3.24 μm) than wide (1.08–1.74 μm), sometimes with small polar aerotopes. Apical cells flat-rounded, rarely conical-rounded; at the top of the apical cell appears to be a small protrusion, probably with ring-like aerotope. Thylakoids arranged peripherally (five to six).','Konstantinou et al. 2021',NULL,0,0),(1966,2276,'diagnosis','Solitary cells or small colonies of 2, 4 or 8 cells surrounded by dense, colorless and slightly lamellate mucilaginous envelopes. Cells, spherical or hemispherical 14–18 μm in diameter with pale-green, blue–green or grey homogeneous to granulate cell contents. Cell division occurring by binary fission in three or more planes, or irregularly in old colonies.','Duval et al. 2021',NULL,0,0),(1967,2277,'diagnosis','Differing from the sister genus <em>Kaipairowitsia </em>ecologically in its occurrence only in desert soils and morphologically by having wider cell dimensions and differing cell shape, cells of <em>Trichotorquatus </em>being in general isodiametric to shorter than wide while cells of <em>Kaipairowitsia </em>are in general longer than wide (Figs. 1-6). <em>Trichotorquatus </em>also lacks the Arthronema-like outgrowths and presence of multiple trichomes in a single sheath typical for <em>Kaipairowitsia</em>. Morphologically, closest to Leptolyngbya sensu stricto, but phylogenetically distant from that taxon.','Pietrasiak et al. 2021',NULL,0,0),(1968,2277,'description','Colony forming a floating mat in liquid culture by capturing oxygen bubbles during photosynthesis, on agar not penetrating the substrate, but occasionally with upright solitary filaments. Filaments always with a single trichome, only rarely producing pseudobranches, flexuous or straight, not typically entangled. Sheath colorless, firm, thin to variable in thickness, adhering tightly to the trichome, sometimes absent at the ends, often forming a distinctive telescoping collar near trichome apices or a telescoping frayed appearance along the mid-region of the filament, often distinctively kinked and bent, persistent after trichome escapes from sheath. Trichomes slightly constricted to constricted at the crosswalls, with constrictions visible only when sheath is absent, up to 4.3 um wide. Cells isodiameteric to longer than wide, rarely shorter than wide (only immediately after cell division), with thylakoids either parietal or in strand-like fascicles extending longitudinally through the centroplasm, typically with nongranular cell contents, sometimes with one or two minute granules visible at the crosswalls, bright turquoise blue-green cell contents in healthy cultures, becoming yellowish in senescent cultures. Apical cells rounded, longer on average than vegetative cells, sometimes with paler coloration, otherwise not morphologically distinct from vegetative cells. Necridia present, often in rows.','Pietrasiak et al. 2021',NULL,0,0),(1969,2277,'etymology','Trichotorquatus L. = Collared trichome, named for the telescoping sheath at the apex of many trichomes forming a collar around the trichome.','Pietrasiak et al. 2021',NULL,0,0),(1970,2278,'description','Morphology in culture: Colony dark turquoise green, flatly spreading on agar medium with few upright solitary filaments (Figs. 1, A–L; 3, A–K; 5, D, E, L and M; 6, D and E). Filaments mostly unbranched, single and double false branching rarely observed, with a single trichome in each sheath, 2.2-7.3 um wide (mean=3.1 um wide). Sheath typically thin, sometimes widened, firm and rigid, sometimes absent, 0.2-2.4 um thick when present, often having a telescoping frayed appearance along the length of the trichome. Trichomes bright turquoise green, distinctly constricted at the crosswalls, fragmenting at necridia or at simple separating cell divisions, 2.1-4.3 um wide (mean= 2.8 um wide). Cells with distinct chromoplasm and centroplasm, with thylakoids either parietal or in strand-like fascicles extending longitudinally through the centroplasm, 0.9-10.0 um long (mean=2.5 um long), dividing cells up to 9.4 um long, with some non-dividing cells abnormally elongated up to 26 um long. Apical cell blue-green, 2.2-32 um long (mean=4.7 um long). Necridia often in rows, forming sections up to 32 um long. Hormogonia very short, often with 1-6 cells, produced under all culture conditions.','Pietrasiak et al. 2021',NULL,0,0),(1971,2279,'etymology','Coquimbo, named for the Coquimbo Region of the Atacama Desert.','Pietrasiak et al. 2021',NULL,0,0),(1972,2279,'description','Morphology in culture: Colony dark turquoise, with occasionally raised solitary filaments (Figs. 2, A–E; 3, L–Q; 5, A and I; 6A). Filaments unbranched, with a single trichome in each sheath, 2.2-3.6 um wide (mean = 2.6 um wide). Sheath sometimes absent, 0.1-0.6 um thick when present, rarely with short telescoping collar near trichome apices, smooth along the length of the filament. Trichomes bright turquoise green, distinctly constricted at the crosswalls, fragmenting at necridia or at simple separating cell divisions, 1.8-3.4 um wide (mean= 2.5 um wide). Cells with distinct chromoplasm and centroplasm, with thylakoids either parietal or in strand-like fascicles extending longitudinally through the centroplasm, 1.2-5.6 um long (mean=2.4 um long), dividing cells up to 4.6 um long. Apical cell pale yellowish green, 1.6-5.0 um long (mean=3.0 um long). Necridia often in rows, forming sections up to 4.9 lm long. Hormogonia short, often with 4-10 cells.','Pietrasiak et al. 2021',NULL,0,0),(1973,2280,'description','Morphology in culture: Colony dark turquoise, with occasionally raised solitary filaments (Figs. 2, F–J; 4, A–F; 5, B, F, J and N; 6, B and F). Filaments unbranched, with a single trichome in each sheath, 1.6-5.6 um wide (mean=2.7 um wide). Sheath sometimes absent, 0.2-3.0 um thick when present, smooth, frequently wide enough to see trichomes clearly. Trichomes bright turquoise green, distinctly constricted at the crosswalls, fragmenting at necridia or at simple separating cell divisions, 1.0-2.8 um wide (mean= 2.1 um wide). Cells with distinct chromoplasm and centroplasm, with thylakoids either parietal or in strand-like fascicles extending longitudinally through the centroplasm, 1.5-5.0 um long (mean=2.9 um long), dividing cells up to 5.4 um long, with some non-dividing cells elongated up to 12.4 um long. Apical cell often more yellowish than vegetative cells, 1.4-6.3 um long (mean=3.2 um long). Necridia often in rows, forming sections up to 11 um long. Hormogonia typically 4-8 cells long.','Pietrasiak et al. 2021',NULL,0,0),(1974,2280,'etymology','Andrei, named in honor of Jim Andre, Director of the Granite Mountains Research Station and good friend of the authors.','Pietrasiak et al. 2021',NULL,0,0),(1975,2281,'description','Morphology in culture: Colony dark turquoise, with occasionally raised solitary filaments (Figs. 2, K–N; 4, G–M; 5, C, G, K and O; 6, C and G). Filaments mostly unbranched, pseudobranches present but rare, with a single trichome in each sheath, 2.0-7.0 um wide (mean=3.1 um wide). Sheath sometimes absent, 0.2-3.0 um thick when present, smooth to rough appearance along the length of the trichome. Trichomes bright turquoise green, distinctly constricted at the crosswalls, fragmenting at necridia or at simple separating cell divisions, 2.0-3.6 um wide (mean= 2.6 um wide). Cells with distinct chromoplasm and centroplasm, with thylakoids either parietal or in strand-like fascicles extending longitudinally through the centroplasm, 1.2-4.0 um long (mean=2.4 um long), dividing cells up to 4.4 um long. Apical cell blue-green, 1.8-4.6 um long (mean=3.1 um long). Necridia often in rows, forming sections up to 12 um long. Hormogonia short, typically under 10 cells long.','Pietrasiak et al. 2021',NULL,0,0),(1976,2281,'etymology','Ladouxae, named in honor of Tasha LaDoux, who facilitated our research in Wonderland of Rocks, Joshua Tree National Park and ever since has been a dear friend of the authors.','Pietrasiak et al. 2021',NULL,0,0),(1977,1056,'etymology','Named for the Kaiparowits Plateau, a major geological formation in the Grand Staircase-Escalante National Monument from which the taxon was isolated.','Mai et al. 2018',NULL,0,0),(1978,1056,'description','Filaments flexuous, entangled, sometimes fasciculated, with one to several trichomes in a common sheath, unbranched. Sheath thin, colorless. Trichomes bent, flexuous, entangled, sometimes forming nodules, less than 2.0 μm wide. Hormogonia and necridia absent. Cells cylindrical, longer than wide, sometimes with outgrowths. End cells rounded.','Mai et al. 2018',NULL,0,0),(1979,1035,'etymology','Pege (Gr): water, stream or spring; thrix (Gr.): hair','Mai et al. 2018',NULL,0,0),(1980,1035,'description','Filaments mostly solitary, at times with multiple hormogonia in a common sheath, or with loose nodule formation, with infrequent double and single false branching. Sheath clear, thin and firm to soft and widened, but never diffluent. Trichomes straight, flexuous, or entangled within a sheath into a loose nodule, sometimes spirally coiled, slightly constricted at the crosswalls, with slow gliding motility observed in trichomes lacking sheath, not tapered. Cells mostly shorter than wide, becoming isodiametric to slightly longer than wide before division, without aerotopes, sometimes with granules in cytoplasm; with parietal thylakoids. Apical cells rounded, without calyptra. Involution cells with axillary bud-like structures rare. Reproduction by trichome fragmentation via disintegration at necridia or without the presence of necridia.','Mai et al. 2018',NULL,0,0),(1981,1036,'description','Colony bright blue green, with radial fasciculation, penetrating the agar. Filaments long or short, sometimes forming nodules (Fig. 10a), or loosely to tightly spirally coiled (Figs. 10b–g), rarely singly (Fig. 10i) or doubly false branched (Fig. 10h), 2.0–6.0 μm wide (to 14 μm wide at nodules). Sheath firm, colorless, usually attached to trichome, occasionally softer, widened (Figs. 10b, i–k), sometimes irregular and stratified (Fig. 10k). Trichomes untapered, more or less constricted at the distinctly visible cross-walls, occasionally with tight, regular, screw-like coils (Fig. 10l), necridia not observed, 1.5–2.5–(3.0) μm wide. Cells slightly shorter than wide to longer than wide, rarely with a single central granule, with parietal thylakoids, 1.0–3.0 μm long. End cells rounded.','Mai et al. 2018',NULL,0,0),(1982,1036,'etymology','bostrychos (Gr.): curl, anything twisted; Latinized to bostrychoides.','Mai et al. 2018',NULL,0,0),(1983,1037,'diagnosis','Morphologically most similar to P. convoluta in the formation of nodules, however, differing from this and other species in the dirty, olive-green coloration of trichomes.','Mai et al. 2018',NULL,0,0),(1984,1037,'description','Colony dark olive-green, hairy, spreading radially, flat and mucilaginous or mounded. Filaments long or short, frequently irregularly bent due to uneven cell division along filament (Fig. 11a–d), false branched (Fig. 11e), sometimes loosely coiled to form irregular nodules (Fig. 11d), 2.0–3.3–(3.7) μm wide. Sheath firm, colorless, usually attached to trichome, occasionally widened (Fig. 11h), up to 1.7 μm wide. Trichomes constricted at indistinctly visible cross-walls, cell division along trichomes often irregular, producing cells with variable shape and width (Figs. 11g–k), with necridia, 1.9–2.8 μm wide in young trichomes, 2.4–3.5 μm wide in actively dividing trichomes. Hormogonia few-celled (Figs. 11h–k). Cells occasionally isodiametric (1.7–2.6 μm long), shorter than wide in meristematic regions (1.1–1.7 μm long), often with a large central granule. End cells typically rounded, but sometimes elongated and/or irregularly shaped (Fig. 11k).','Mai et al. 2018',NULL,0,0),(1985,1038,'diagnosis','Differing from other species in the genus based on the frequent formation of loose irregular nodules. Distinguishable from <em>P. indistincta</em> in the cytosine residue opposite the basal 3’ unilateral bulge of the D1-D1’ helix (Figs. 6c, d) and the V3 helix sequence and structure (Figs. 9c, d). Some similarity with <em>P. bostrychoides</em> and<em> P. olivacea</em> in nucleotides 1–15 on the 5’ strand and their complement was observed, but the absence of the V2 helix and other dissimilarities clearly set them apart.','Mai et al. 2018',NULL,0,0),(1986,1038,'description','Colony bright blue green, radially spreading, growing into the agar. Filaments fasciculated, long, sometimes singly or doubly false branched (Fig. 12a), straight or slightly bent (Figs. 12a–b, e), frequently forming loose to compact nodules (Figs. 12b–c), 1.4–3.9–(4.9) μm wide. Sheath firm, colorless, usually attached to trichome (Fig. 12e), occasionally widened (Figs. 12d–e), rarely irregular and stratified, up to 1.3 μm wide. Trichomes untapered, not or slightly constricted at distinctly visible cross-walls, with necridia (Figs. 12b, e–f), lacking meristematic zones, with cell division occurring throughout trichome, 1.3–2.5 (3.2) μm wide. Hormogonia few-celled (Fig. 12a). Cells slightly shorter than wide to longer than wide, sometimes with a single central granule, with parietal thylakoids, 1.0–2.5–(3.7) μm long. End cells rounded.','Mai et al. 2018',NULL,0,0),(1987,1039,'diagnosis','Morphologically intermediate between other species, differing in the absence of spiraling and nodule formation; with conserved ITS domains almost identical in shape to D1-D1’ helix of P. convoluta (Fig. 6d). Distinguishable from this species in the adenine residue opposite the basal 3’ unilateral bulge of the D1-D1’ helix and sequence from position 1–15/69–90 (Figs. 6d), and the V3 helix sequence and structure (Figs. 9d).','Mai et al. 2018',NULL,0,0),(1988,1039,'description','Colony bright blue green or olive-green. Filaments long, with variation in width between young and mature trichomes (Figs. 13a), rarely singly or doubly false branched (Figs. 13a–b), rarely with more than one trichome sharing a common sheath (Fig. 13c), 2.3–4.0 μm wide. Sheath firm, usually attached to trichome, occasionally widened, rarely irregular and stratified (Fig. 13d), absent in immature filaments or hormogonia. Trichomes untapered, not or slightly constricted at distinctly visible crosswalls, with necridia (Figure 13c–d, f), with meristematic zones, 1.9–3.3 μm wide. Hormogonia short (Figs. 13e–f). Cells typically isodiametric, often shorter than wide especially in meristematic zones (Fig. 13f), slightly longer than wide in young trichomes (Fig. 13a–b), (1.3)–1.7–2.7 μm long. End cells rounded.','Mai et al. 2018',NULL,0,0),(1989,1040,'etymology','Drouetiella: named in honor of Francis Drouet, a prominent North American phycologist of the late 20th century whose monographic works still serve as a primary bibliographic reference into the nomenclature of the cyanobacteria.','Mai et al. 2018',NULL,0,0),(1990,1040,'description','Filaments mostly solitary, at times consolidated into fascicles, with infrequent single false branching. Sheath clear, thin, and firm, occasionally widened. Trichomes untapered, straight, flexuous, or spirally coiled, but not in nodules, slightly constricted at the crosswalls. Cells mostly longer than wide, becoming isodiametric to slightly shorter than wide in dividing trichomes, without aerotopes, rarely with a central granule in the cytoplasm; with parietal thylakoids. Apical cells cylindrical, untapered, rounded, without calyptra. Reproduction by trichome fragmentation via disintegration without necridia.','Mai et al. 2018',NULL,0,0),(1991,2282,'description','Colonies microscopic, usually small, regular cubic, with 8–16 cells, more or less grouped together; sometimes large colonies composed of sub–colonies; colonies olive–green or red–brown, surrounded by mucilaginous envelopes; mucilage fine, homogeneous and colorless; cells usually spherical or hemispherical after division, with granular content, blue–green, grey–green, olive–green, yellowish, or red–brown; cells arranged three–dimensionally in perpendicular rows and divide regularly in three perpendicular planes in subsequent generations; thylakoids irregularly arranged.','Geng et al. 2021',NULL,0,0),(1992,2282,'diagnosis','Using light microscopy, this species appears morphologically similar to the genus Eucapsis regarding colonial form and cellular spatial arrangement. However, the phylogenetic tree produced from 16S rRNA gene sequences indicated that this species held a unique position in the family Chroococcaceae and was close to the recently established genus Cryptococcum but separated from the Chroococcus ‘sensu stricto’ clade and Eucapsis. In addition, the 16S rRNA sequence of this strain showed low similarity with those of Eucapsis spp. and of the genus Cryptococcum, and significant differences in the secondary structure of the 16S–23S ITS region also supported the establishment of this new cyanobacterial genus.','Geng et al. 2021',NULL,0,0),(1993,2283,'description','Colonies are microscopic, small, more or less regular cubic, typically with 8–16 cells, sometimes grouped together, large colonies composed of subcolonies. Colonies are surrounded with mucilage, but single cells are not. Mucilage fine, homogeneous, colorless, not stratified or diffluent; cells hemispherical to rounded, sometimes oval, with a diameter of 8.44–(10.25)–12.32 μm; content granular, blue–green, grey–green, or olive–green in growth phase, and yellowish, yellow or red–brown in decline phase; cells arranged three–dimensionally in perpendicular rows and divided regularly in three perpendicular planes in the subsequent generation, more often forming cube colony morphology of eight cells. Thylakoids are irregularly arranged at the periphery of cells (Fig. 2). Ecology: this species is planktic and inhabits mesotrophic water.','Geng et al. 2021',NULL,0,0),(1994,2283,'diagnosis','<em>gongqingensis </em>comes from Latin “gongqing”, which refers to the Gongqing city where the strain was collected.','Geng et al. 2021',NULL,0,0),(1995,2284,'description','Thallus dense, erect, forest green in color, with heteropolar trichomes. Filaments with sheath, fasciculate, straight or bent, slightly tapering, with Scytonemataceae–type false branching. Filaments 15.7–22.9 μm wide (19.5 ± 2.1 μm). Sheath thin, thicker near branching, hyaline, 3.2 ± 1.2 μm wide. Trichomes cylindrical, straight, slightly constricted at cross–walls, 12.4–20.2 μm wide (16.4 ± 1.8 μm). Cells somewhat isodiametric, light green to dark grey or orange in color, granulated, highly vacuolated, 12.4–20.2 μm wide × 5.1–10.1 μm long. Apical cells rounded, calyptra not present. Heterocytes common, intercalary, square and sometimes flattened, 12.1–18.3 μm wide × 5.3–11.7 μm long. Akinetes not present. Reproduction by motile and aerosolizing hormogonia.','Barbosa et al. 2021',NULL,0,0),(1996,2284,'etymology','“fioreae” (L.) is an epithet that honors Dr. Marli de Fátima Fiore for her dedication and work on cyanobacterial systematics, genetics, and bioactive compounds.','Barbosa et al. 2021',NULL,0,0),(1997,2285,'description','Thallus dense, erect, green to dark grey in color. Filaments often fasciculate, straight or bent, slightly tapering, with Scytonemataceae–type false–branching, 19.2–26.1 μm wide (22.9 ± 2.2 μm). Sheath thin, hyaline to yellow brown, often encrusted, 4.7 ± 1.3 μm wide. Trichomes cylindrical, straight to flexuous, slightly constricted at cross–walls, 13.0–21.4 μm wide (18.2 ± 2.4 μm). Cells isodiametric, sometimes wider than long, green to reddish brown in color, granulated, highly vacuolated, 13.0–21.4 μm wide × 5.9–13.4 μm long. Apical cells are rounded and blunt, calyptra present. Heterocytes common, intercalary, square and sometimes elongated, 20.3–26.1 μm wide × 12.4–18.2 μm long. Akinetes not present. Hormogonia rare or not present.','Barbosa et al. 2021',NULL,0,0),(1998,2285,'etymology','“santannae” (L.) is an epithet that honors Dr. Celia Leite Sant’Anna for her dedication and work in cyanobacterial systematics and taxonomy.','Barbosa et al. 2021',NULL,0,0),(1999,2286,'description','Thallus dense, erect, composed of heteropolar trichomes, olive green in color. Filaments often fasciculate, straight or bent, slightly tapering, with Scytonemataceae–type false–branching, 24.1–29.9 μm wide (26.6 ± 2.1 μm). Sheath occasionally thick, extends past filament, hyaline, 4.5 ± 1.5 μm wide. Trichomes cylindrical, straight, and slightly constricted at cross–walls, 19–26.7 μm wide (22.6 ± 2.6 μm). Cells isodiametric, sometimes wider than long, light brown to reddish brown in color, granulated, highly vacuolated, 19.0–26.7 μm wide × 7.6–14.4 μm long. Apical cells are rounded, calyptra is present. Heterocytes are common, intercalary, square and elongated, 18.6–26.5 μm wide × 6.3–17.6 μm long. Akinetes not present. Reproduction by hormogonia.','Barbosa et al. 2021',NULL,0,0),(2000,2286,'etymology','“wernerae” (L.) is an epithet that honors Dr. Vera Regina Werner for her dedication and work on the study of cyanobacterial systematics and taxonomy.','Barbosa et al. 2021',NULL,0,0),(2001,2287,'description','Morphologically two types of cyanobacteria, with coccoid cells solitary or in groups and with uniseriate solitary trichomes. Solitary cells spherical to rod–shaped with rounded ends, with or without mucilage, without sheaths, divided by binary fission in one plane or into two perpendicular planes in successive generations. Trichome cells longer than wide, with rounded or flattened apical cells, without sheaths. Thylakoids radial, semi radial, irregular in the transverse plane, and parallel in the longitudinal plane.','Tuji et al. 2021',NULL,0,0),(2002,2288,'description','Trichomes solitary, planktic, uniseriate without false branching, straight or waved, not constricted at the cross–walls, immotile, without sheaths, 30–40 μm long, but up to several hundred μm long in cluture. Cells blue–green to pale blue–green, with scattered granules, usually long cylindrical, 1.2–3.5 μm wide and 4.6–16.2 (−26.7) μm long, 1.5–11.1 as long as width. Apical cells rounded or flattened. Necridic cells, calyptra, aerotopes, akinetes and heterocytes not observed. Thylakoids peripherally radial in the transverse plane, parallel in the longitudinal plane. Cells produces microcystin.','Tuji et al. 2021',NULL,0,0),(2003,2289,'description','Dark greenish, soft spongy, macroscopic mats were found to grow in submerged condition by adhering to the wall of the hot spring in natural condition. In pure culture condition, colonies grow as bluish green creeping mat on solid media, while a clumped appearance was visible in the liquid medium. Usually, filaments are densely entangled to each other. Filaments are uniseriate, and branches appear from both the sides of the filament. Initiation of branching can be seen even in young filaments. Typical T-type true branching is prominent though at some places, false branching is also seen. However, V or reverse Y-type branching was never been observed. Branches are usually narrower than the main filaments and also exhibit tapering ends with elongated cells. The vegetative cells of the main axis exhibit granular cytoplasm and their shape varies from globose to spherical having deep constrictions at the cross walls but sometimes there was a little bit distortion in the branch primordial cells. The vegetative cells of the main filament are 5.2–8.0 μm in length and 6.5–8.5 μm in width, whereas the size of the vegetative cells of the branches is varied from initial to terminal position. The size of the initial cell of the branch is 5.2–6.8 μm in length and 7.5–8.2 μm in width, whereas the size of the terminal cells ranges from 5.5–6.6 μm in length and 3.5–4.5 μm in width. Heterocytes are prominent and can be intercalary, terminal and lateral sessile and the shape varies from spherical, cylindrical to barrel shaped. Intercalary heterocytes 5.5–7.8 μm in length to 5.2–8.0 μm in width. Lateral heterocytes are slightly smaller than the others, i.e., 4.8–6.0 μm in length to 5.0–6.5 μm in width and are circular to oval in shape with slightly broader base. Terminal heterocytes 5.2–5.5 μm in length to 5.0–5.5 μm in width. Circular monocytes are 8.2–10.0 μm in length and width and emerging from the main filaments and comparatively larger in size. Akinetes and hormogonia were not visible.','Jaiswal et al. 2021',NULL,0,0),(2004,2289,'diagnosis','The strain TA-9 exhibits prominent T-type branching, rare false branching and distinctive positioned heterocytes (intercalary, terminal and lateral sessile) and the above said features show significant differences from <em>Mastigocladus laminosus</em> having T-type and reverse Y-type of branching pattern with only intercalary heterocytes (Fig. 1a, j; Online Resource 2). The presence of lateral sessile heterocytes, which is smaller than intercalary and terminal heterocytes, is typical distinctive character of this novel species (Fig. 1e, g; Table 2). The branches of strain TA-9 have less tapered ends as compared to M. laminosus. Monocytes are present, whereas hormogonia and akinetes are not detected. Monocytes are larger than the heterocytes and the vegetative cells (Fig. 1j). Phylogenetically, the strain TA-9 establishes single clade with other thermal isolates of true branching but on separate node (Fig. 3). Secondary structures of the ITS region of strain TA-9 prove significant differences from the other phylogenetically closely related taxa (Fig. 4 and Fig. 5).','Jaiswal et al. 2021',NULL,0,0),(2005,2289,'etymology','The epithet ambikapurensis (am.bi.ka.pu.ren’sis. N.L. masc. adj.ambikapurensis) refers to district Ambikapur from where the strain was isolated.','Jaiswal et al. 2021',NULL,0,0),(2006,322,'diagnosis','Emended diagnosis: Thallus pulvinate or wooly, up to 1.5 cm thick, greyish blue with multiple densely coiled, or parallel-arranged filaments, sometimes joined into erect fascicles. Filaments irregularly branched, sometimes distinctly morphologically diversified in basal sections and branches. Trichomes uniseriate, isopolar, with vegetative cells usually longer than wide, cylindrical, not constricted or slightly constricted at cross walls, not attenuated towards the ends, with rounded terminal cells. Cell content blue-green, often with granulation of various graininess and/or with prominent vacuole-like rounded structures. Branching of two types, true branching of Y-type (reverse Y-branching originates always from special oblong cells within basal sections, each followed by two shortened cells, from which one divides into one elongated cell that starts the lateral branch) and/or T-type (initiates at two swollen, globose cells with prominent, vacuole-like and granular inclusions that divide into smaller, rounded to isodiametric cells that start the lateral branch) and false-branching of scytonematoid-type (including necridic cells); branching initiates remote from the heterocytes. Sheaths firm, homogeneous or slightly lamellated, yellow-brown in color in mature parts. Vegetative cells blue-green in color with slightly granular content. Heterocytes intercalary, cylindrical, solitary. Akinetes not observed. Cell division crosswise to the trichome length. Reproduction mostly by hormogonia, separating from trichome apices or defragmentation of, especially, the lateral branches. A small genus with three species currently taxonomically accepted: S. cavernicolum from a cave in Spain [10], S. kaboorum from the littoral zone of an acidic, coastal oligotrophic lake in Australia [11], the former type species of the genus S. sinense [12] from wet, calcareous rocks of China and S. sinense var. minor from Papua New Guinea [13] but without any of them being deposited at culture collections nor available genetic information. Two sequenced isolates from soil in Papua New Guiana that were not taxonomically defined supported the distinct phylogenetic position of this genus [2].','Jung et al. 2021',NULL,0,0),(2007,2290,'description','Pulvinate macroscopic thallus, up to 1 cm thick, dark green, wooly, that dyes liquid medium transparent-brownish during aging. Filaments are interwoven, on agar first creeping, later slightly erect and parallel arranged. Two types of filaments can be distinguished from each other, swollen basal branches and thin lateral branches. Basal branches: trichomes 3.3–6.6 um wide, with necridia, mostly uniseriate, bloated but tapered/waisted towards heterocytes that were always present in medium with and without nitrogen; cells barrel-shaped, rounded, squeezed, constricted at cross-walls, wider than long, 2.4–3.3 (6) um  1.3–1.7um, coarse granulated, with at least one big vacuole-like structure in each cell, blue-green. Lateral branches: up to 200 um long, uniseriate, without necridia; filaments straight, parallel; regular, not tapered towards the ends, fine granulated, fine vacuolated, cells regular, quadratic or slightly longer than wide, 2–2.3 um  2–2.8 um, very slightly constricted at cross-walls, blue-green; apical tip rounded to slightly conical, yellowish, 2.8 m  1.8 um. Branching patterns are of true-branching T-type towards all sides of the basal section and false-branching (scytonematoid). Heterocytes are frequent independent of the culture medium used which occur solitary or rarely in pairs of two. They are thick-walled, yellow, intercalary and rectangular in lateral branches, 2.3 um  3.6–5 (8.5) um but sub-globose, squeezed and bloated in basal sections, 2–2.2 um  3.6–3.9 um. Sheaths of the trichomes are hyaline, colorless, firm, limited, not lamellated, very tight but ruptured by the apical cells of lateral branches. Mature cultures with limited, hyaline but much wider sheaths. Hormogonia or akinetes were not observed, fragmentation of lateral branches (tips) as main dispersal pattern (Figures 1 and 2; Table 1).','Jung et al. 2021',NULL,0,0),(2008,2290,'etymology','‘bifilamentata’—‘having two types of filaments’, due to the clear morphological separation of the species into basal and lateral sections','Jung et al. 2021',NULL,0,0),(2009,2291,'description','Filaments fasciculate and collectively unidirectional, phototactically oriented. Main filaments isopolar, cylindrical, uniseriate, straight to bent, 8 – 18 μm in diameter, main filament generally wider than lateral filaments which gradually attenuate to a bluntly conical, bent end; with single and/or geminate false-branching. Filament end with facultative terminal widening of sheath. Sheath thin, colorless to yellow/orange. Young developing filaments with thin hyaline sheath, older sheath wider and yellow/orange. Young and developing lateral filaments blue-green with cells and heterocytes longer than wide. Young lateral filaments spread, with single and germinate false branching. Older lateral filaments with thicker sheath, cells with vacuoles, and fasciculate. Horizontal or lead filaments with thicker sheath, cells and heterocytes wider than long. Vegetative cells isodiametric to shorter than wide, slightly constricted at cross walls, 3.3–8.2 μm long × 18.0–27.5 μm wide in the main filament, 3.5–5.0 μm long × 4.2–12.0 μm wide in lateral filaments. Heterocytes basal and intercalary, solitary, rectangular to compressed-ovoid, 6.3–9.5 μm long × 11.0–19.0 μm wide. Akinetes absent. Cell content blue-green to green with granulation or an enlarged individual vacuole. Spherical cellular inclusions within vegetative cells are a diacritical marker.','Berthold et al. 2021',NULL,0,0),(2010,2291,'etymology','“<em>tapete</em>” (L. carpet) refers to the ability of this cyanobacterium to form thick carpet-like mats','Berthold et al. 2021',NULL,0,0),(2011,2292,'diagnosis','Thallus densely arranged, entangled in macroscopic crusts among other algae and cyanobacteria, initially ± fruticose, later irregularly flattened, crispy or wavy, up to several cm in diameter, olive-green, yellow brown to brown to dark brown. Thallus in fascicles or bush-like. Filaments isopolar, uniseriate, cylindrical, straight or flexed, 25–43 μm (up to 62 μm with two trichomes at same filament) in diameter, main filament generally wider than the lateral filaments; with single or geminate false-branching. Sheath firm, layered with changeable thickness, yellowish to yellow-brown, closed at the apex. Ends of trichomes sometimes overlap the sheaths. Terminal vegetative cells (15.5)16.9–20.7(21.5) μm wide and (5.5)6.1–9.2(10.0) μm long, with perfectly rounded ends. Vegetative cells cylindrical or slightly constricted at the cross walls, (16.5)17.1–21.4(22.0) μm wide, (4.0)4.8–7.7(8.0) μm long in the main filament, (12.5)13.0–15.6(16.0) μm wide, (4.0)4.3–6.0 μm long in lateral branches, with granular polyphosphate inclusions. With age, cells generate vacuole-like structures, which can fill the entire cell, sometimes in rows of neighbouring cells. Apical cells rounded and in terms of shape distinct from other vegetative cells. Heterocytes intercalary, solitary, barrel-shaped to compressed-ovoid, 12.0–13.5(14.1) μm long and 15.0–19.0 μm wide. Akinetes absent. Reproduction by disintegration of the thallus or by hormogonia.','Maltsev et al. 2021',NULL,0,0),(2012,2292,'etymology','‘sahyadrensis’ reflects the term Sahyadri, which is another name of the mountain range Western Ghats','Maltsev et al. 2021',NULL,0,0),(2013,2293,'description','Homocytous, uniseriate, filamentous cyanobacteria. Thalli prostrate, sometimes fascicular, on submerged and/or exposed marine littoral substrata, and floating unconsolidated substrate. Trichomes with constriction every even number of cells. Cells discoid, sheath lacking, apical cells range from bluntly rounded, to conical rounded, to rounded. Reproduction by hormogonia and fragmentation. &nbsp;','Berthold et al. 2021',NULL,0,0),(2014,2293,'diagnosis','Monophyletic group of marine genera based on the 16S rRNA sequence phylogenies, sister to the clade containing <em>Dapis</em>, <em>Okeania</em>, and <em>Trichodesmium </em>as well as the sister clade containing <em>Affixifilum</em>, <em>Limnoraphis</em>, and <em>Neolyngbya</em>.','Berthold et al. 2021',NULL,0,0),(2015,2294,'description','Homocytous filamentous cyanobacteria, forming dark green or red/purple prostrate, sometimes fascicular thallus, on submerged and/or exposed marine littoral substrata and floating mats. Trichomes uniseriate, cylindrical, constricted at cross-walls of even number of cells (2, 4, and 8), attenuated at ends, sheaths absent, flexuous and motile. Cells discoid, shorter than wide, apical cell rounded, narrowed at times, with occasional calyptra. Cell content light to dark green, blue green, or pink or red, with sparse vacuoles, facultative granulated cross-walls. All cells capable of division. Reproduction by fragmentation, necridia, and hormogonia.','Berthold et al. 2021',NULL,0,0),(2016,2294,'diagnosis','Genus is delimited by ecology, morphology, and molecular and phylogenetic analyses based on the 16S rRNA gene sequence and characteristic 9-base pair insert within the 16S rRNA gene.','Berthold et al. 2021',NULL,0,0),(2017,2294,'etymology','“<em>Leptochromothrix</em>” (G.) is in reference to the thin and colorful filaments: “<em>lepto</em>” thin, “<em>chromo</em>” colorful, “<em>thrix</em>” hair.','Berthold et al. 2021',NULL,0,0),(2018,2295,'description','Thallus dark green and prostate, sometimes fascicular. Trichomes cylindrical, very flexuous, with constriction every even number of cells, 8.7–9.9 μm in diameter, facultative attenuation. Cells discoid, wider than long, 2.2–3.8 μm long; apical cell bluntly rounded, with occasional calyptra. Cell content light to dark green or blue green, with sparse vacuoles; Cross-walls heavily granulated, prominent in young or older filaments, and noticeable every even number of cells. Reproduction by hormogonia.','Berthold et al. 2021',NULL,0,0),(2019,2295,'diagnosis','Species delimited by morphology and molecular and phylogenetic analyses based on the 16S rRNA gene and 16S-23S rRNA ITS region, unique 9-base pair insert within the 16S rRNA gene.','Berthold et al. 2021',NULL,0,0),(2020,2295,'etymology','“<em>valpauliae</em>” is named in honor of Dr. Valerie J. Paul for her substantial contribution to the study of marine cyanobacteria and their chemical ecology.','Berthold et al. 2021',NULL,0,0),(2021,2296,'diagnosis','Species delimited by morphology and molecular and phylogenetic analyses based on the 16S rRNA gene and 16S-23S rRNA ITS region, distinctive 9-base pair insert within the 16S rRNA gene.','Berthold et al. 2021',NULL,0,0),(2022,2296,'description','Thallus light to dark red to purple, prostrate, sometimes fascicular. Trichomes cylindrical, straight to flexuous, with slight constriction between individual cells and extensive constriction between every two cells, 8.8–9.9 μm in diameter, facultative attenuation. Cells discoid, wider than long, 3.3–5.0 μm long; apical cell bluntly rounded, with occasional calyptra. Cell content light to dark pink to red, with large or many small vacuoles; cross-walls granulated throughout trichome development. Reproduction by hormogonia.','Berthold et al. 2021',NULL,0,0),(2023,2296,'etymology','“<em>engenei</em>” is in honor of Dr. Niclas Engene for his contributions to marine cyanobacterial taxonomy and natural products research.','Berthold et al. 2021',NULL,0,0),(2024,2297,'description','Homocytous filamentous cyanobacteria, forming light to dark olive green planktic trichomes or intertwined within floating prostrate mats of unconsolidated substrate near mangroves. Trichomes uniseriate, cylindrical, coiling, and flexuous, slightly constricted at cross-walls of even number of cells (2, 4, and 8), facultative attenuation, sheaths absent. Cells discoid, shorter than wide; apical cell conical rounded, without calyptra. Cell content olive green, light blue-green, facultative granulated cross-walls. All cells capable of division. Reproduction by fragmentation, necridia, and hormogonia.','Berthold et al. 2021',NULL,0,0),(2025,2297,'etymology','“<em>ophiophycus</em>” (G.) is in reference to the snake-like appearance of filaments, where apical cells may have two large vacuoles that resemble eyes. “<em>ophio</em>” snake, “<em>phycus</em>” algae','Berthold et al. 2021',NULL,0,0),(2026,2297,'diagnosis','Genus is delimited by ecology, morphology, and molecular and phylogenetic analyses based on the 16S rRNA and 16S-23S rRNA ITS region.','Berthold et al. 2021',NULL,0,0),(2027,2298,'description','Thallus light to dark olive green, flaky and loose, coiled, prostrate. Trichomes cylindrical, straight to very flexuous, slightly constricted or extensive constriction every 2, 4, and 8 cells; motile, 12.6–15.4 (19.6) μm in diameter; attenuated. Cells discoid, wider than long, 2.4–4.4 μm long; apical cell conical and rounded. Cell content olive green, grey, blue-green, purple; cross-walls finely granulated. Reproduction by fragmentation hormogonia.','Berthold et al. 2021',NULL,0,0),(2028,2298,'diagnosis','Species delimited by morphology and molecular and phylogenetic analyses based on the 16S rRNA gene and 16S-23S rRNA ITS region.','Berthold et al. 2021',NULL,0,0),(2029,2298,'etymology','“<em>aerugineus</em>” (L.) is a reference to the crystal blue green coloration of the trichomes.','Berthold et al. 2021',NULL,0,0),(2030,2299,'description','Homocytous filaments, forming light to dark black, prostrate, sometimes fascicular thallus, on submerged and/or exposed marine littoral substrata, epilithic on limestone or epipelic on sand and silt forming mats within mangroves. Trichomes uniseriate, cylindrical, straight to flexuous, highly constricted in even number of cells (2, 4, 8, and 16) in younger trichomes, while less constricted or not in older, facultative attenuation with bent ends, sheaths absent; highly motile and oscillate by bending and rotating counterclockwise at ends. Cells discoid, shorter than wide, apical cell rounded, blunt and narrowed, with occasional yellow calyptra. Cell content red, rust, light to dark green, purple, grey, yellow, gold, brown, facultative granulated crosswalls. All cells capable of division. Reproduction by fragmentation, necridia, and hormogonia.','Berthold et al. 2021',NULL,0,0),(2031,2299,'etymology','“<em>Vermifilum</em>” (L.) is a reference to the worm-like appearance of trichomes as they rotate and creep. “<em>vermi</em>” worm, “<em>filum</em>” filament.','Berthold et al. 2021',NULL,0,0),(2032,2299,'diagnosis','Genus is delimited by ecology, morphology, molecular and phylogenetic analyses based on the 16S rRNA gene sequence and 9-base pair insert within the 16S rRNA gene sequence.','Berthold et al. 2021',NULL,0,0),(2033,2300,'diagnosis','Species delimitated by characteristic D1-D1′ and Box B secondary structures of the 16S-23S rRNA ITS and the 16S-23S rRNA ITS percent dissimilarity.','Berthold et al. 2021',NULL,0,0),(2034,2300,'description','Thallus light to dark golden brown to black, prostrate or sometimes fascicular. Trichomes cylindrical, straight to flexuous, wavy at times, intensely motile, bent and rotating at ends, slightly constricted or extensive constriction every even 2, 4, 8, and 16 cells; 9.7–14.6 μm in diameter. Cells discoid, wider than long, 1.9–4.1 μm long; apical cell bluntly rounded with occasional yellow calyptra. Cell content homogenous, light green, grey to dark grey, gold, reddish-brown and purple in younger cells while dark purple, brown and magenta in older ones, sometimes with large vacuoles; cross-walls granulated. Reproduction by fragmentation and hormogonia.','Berthold et al. 2021',NULL,0,0),(2035,2300,'etymology','“<em>ionodolium</em>” (L.) is in reference to purple pigmentation of cells grouped in “barrels” in mature trichomes. “<em>iono</em>” violet-colored, “<em>dolium</em>” barrel.','Berthold et al. 2021',NULL,0,0),(2036,2301,'diagnosis','<em>Affixifilum </em>resembles closely related genera, such as <em>Neolyngbya </em>and <em>Capilliphycus</em>. However, molecular analyses place this genus in a separate clade based on 16S rRNA phylogeny, as well as distinct 16S-23S rRNA ITS secondary structures. This genus is found in shallow tropical marine waters as attached mats, while Neolyngbya is found in both tropical and subtropical waters attached to substrates. Diagnostic features include intense granulation, noted in both the Florida (USA) and Brazilian populations, as well as the formation of<br>multiple terminal hormogonia by apical attenuation, a feature not seen in closely related genera.','Lefler et al. 2021',NULL,0,0),(2037,2301,'description','Thallus forms dense, attached mats. Filaments straight to wavy, isopolar, unbranched. Trichomes cylindrical and slightly constricted at cross walls, attenuation common, surrounded by sheath. Sheath hyaline thin or thick, lamellate. Cells short and discoidal. Cell contents densely granulated, gas vesicles present. Cross walls granulated. Apical cells rounded, calyptra common, attenuating when forming hormogonia. Hormogonia formed within trichomes by straight fragmentation with or without necridia. Terminal hormogonia formed by attenuation of the apices and formation of several hormogonia.','Lefler et al. 2021',NULL,0,0),(2038,2301,'etymology','Reference to the affixing nature of the cyanobacterial mats.','Lefler et al. 2021',NULL,0,0),(2039,2302,'description','Filaments straight 10.9–12.5 um diam. Sheath hyaline, thin or thick, sometimes lamellate. Trichomes purple to golden, slightly constricted at cross walls, 8.7–10.1 um diam. Cells short, 1.1–1.6(2.2) um long. Cell content purple to maroon, slightly gold in some cases, densely granulated. Cross walls granulated with large granules. Apical cells rounded, calyptra uncommon. Hormogonia formed by straight fragmentation with or without necridic cells.','Lefler et al. 2021',NULL,0,0),(2040,2302,'etymology','in honor of the state of Florida (USA)','Lefler et al. 2021',NULL,0,0),(2041,2304,'description','Thallus spreading, flat, forming dark brown-green mats. Filaments mostly single, straight to wavy with no observed false branching. Sheath colourless, smooth and lamellated, 1.0–2.1 μm wide. Trichomes constricted at the cross-walls, granulated, yellow or brown coloured. Cells discoid, typically 12.9–16.5 μm wide and 0.6–2.0 μm long. Apical cells widely rounded, sometimes attenuated with calyptra. Hormogonia formed through straight fragmentation of trichomes and observed to emerge from sheath. Separation discs and necridic cells occasionally present.','Curren et Leong 2018',NULL,0,0),(2042,2305,'description','Filaments straight, 13.1–15.4 (17) um diam. Sheath hyaline, thick, occasionally lamellate. Trichomes amber to brown, slightly constricted at cross walls, (9) 11.0–12.6 lm diam. Cells short, 1.51–2.0 um length. Cell content green to amber, heavily granulated at cross walls, aerotopes facultative. Apical cells rounded, sometimes capitate, can be larger than other cells and appear empty. Hormogonia formed by straight and uneven fragmentation via necridic cells.','Berthold et al. 2021',NULL,0,0),(2043,2306,'description','Filaments straight, (15.7) 18.2–24.6 (31) um diam, sheath hyaline, thick. Trichomes emerald green, slightly constricted at cross walls, (14) 16.1–21.3 (25) um diam. Cells short (1.5) 2.0–2.8 (3.6) um length. Cell content green, with aerotopes and granules. Granulation at cross walls. Apical cells rounded, can be larger than other cells, lacking pigments, and containing aerotopes. Hormogonia formed by straight fragmentation and<br>uneven fragmentation, via necridic cells.','Berthold et al. 2021',NULL,0,0),(2044,2306,'diagnosis','“biscaynensis” is a reference to Biscayne Bay where the sample was collected.','Berthold et al. 2021',NULL,0,0),(2045,2307,'description','Unicellular and colonial cyanobacteria. Cells elongated, without prominent mucilaginous envelopes with few parietal thylakoids. Thermophilic (up to over 80 °C).','Komárek et al. 2020',NULL,0,0),(2046,2309,'description','Cyanobacterial cells solitary, in irregular agglomerations, or in short, few–celled indistinct rows, narrow, with rounded ends, usually several times longer than wide, straight, strictly cylindrical or slightly curved or arcuated, without prominent slime envelopes. Cell division perpendicular in one plane in subsequent generations, symmetrical or slightly asymmetrical, with daughter cells usually separating soon after division, less frequently forming short rows of a few cells. Cytoplasm sometimes with visible narrowed peripheral chromatoplasma (= few, ± parietal thylakoids), usually pale or intensely olive–green or blue–green, without aerotopes, usually with solitary granules situated in the terminal parts of cells.','Komárek et al. 2021',NULL,0,0),(2047,2309,'eco_distro','','Komárek et al. 2020',NULL,0,0),(2048,416,'description','Unicellular photosynthetic prokaryotes with elongated cells and with 1–4 parietally arranged thylakoids, without gelatinous envelopes. Reproduction by binary fission of cells, perpendicular to the long axis of the cell. At present this family comprises the genera Prochlorococcus, Parasynechococcus and Cyanobium, which differ mainly by phylogenetic markers, by modifications in arrangement of thylakoids in cells and partly by ecology (marine vs. freshwater ecosystems).','Komárek et al. 2020',NULL,0,0),(2049,278,'description','Oxygenic photoautotrophs possessing divinyl chlorophylls–a and –b as their principal photosynthetic pigments. Cells lacking mucilage, spherical to rod shaped just prior to division, cells individual or in pairs, dividing by transverse binary fission, with peripheral photosynthetic thylakoids closely appressed to one another.','Komárek et al. 2020',NULL,0,0),(2050,278,'etymology','Latin<em> Pro</em>=before, <em>chlorococcu</em>s=green coccoid, named for the presence of chlorophyll–b, and idea that this taxon could be the predecessor of chloroplasts in green algae.','Komárek et al. 2020',NULL,0,0),(2051,590,'description','Cells 0.6 to 0.8 μm in diameter, 1.2 to 1.6 μm in length just prior to division.','Komárek et al. 2020',NULL,0,0),(2052,418,'description','Planktic, marine, solitary picocyanobacterial cells without prominent slime envelopes, subspherical up to slightly elongated and short rod–like, maximally 2.5 μm long, with 1–4 parietally arranged thylakoids, without gas vesicles. Reproduction by ± symmetrical binary fission, perpendicular to the longer axes of the cells, in one division plane in the following generations.','Komárek et al. 2020',NULL,0,0),(2053,418,'etymology','Gr. <em>Para </em>= similar to; <em>Parasynechococcus</em> = similar to Synechococcus','Komárek et al. 2020',NULL,0,0),(2054,2332,'description','Cells planktic, marine, solitary, (0.4)0.6–1.2(2.1) μm long, 0.4–0.8 μm wide. Mucilaginous envelopes absent or facultatively forming a very narrow, diffluent and indistinct layer around individual cells. Cytoplasm with (1)2–4 parietal thylakoids, each a little distant from one another, with white bodies between thylakoids in the cells probably corresponding to polyphosphate inclusions, with a few small cyanophycin granules and numerous ribosomes in the centroplasma (Fig. 3A). Cyanophages sometimes seen adsorbed on the cell wall.','Komárek et al. 2020',NULL,0,0),(2055,2332,'etymology','referring to the dark water of open ocean in the Sargasso Sea','Komárek et al. 2020',NULL,0,0),(2056,2334,'description','Unicellular photosynthetic prokaryotes with rod–like cells and with 1–4 parietally arranged thylakoids, without or with very slight, colourless and diffluent gelatinous envelopes. Reproduction by crosswise, sometimes asymmetrical cell division. Living solitary or in irregular groups. The family is currently comprised of only one genus, <em>Thermosynechococcus </em>gen. nov.','Komárek et al. 2020',NULL,0,0),(2057,330,'description','Cells solitary or in irregular groups (or strata on the substrate), without prominent slime envelopes, oval, cylindrical, straight or slightly curved, with ± homogeneous content, rounded or truncated at the ends, (3.0)4.0–17.0(32.0) μm long and 1.1–3.0(4.8) μm wide, with parietal thylakoids. The cell length is variable, sometimes also within the same population. The cells sometimes remain in short, few–celled, filamentous–like formations. Reproduction by binary fission, perpendicular to the long axis of the cells, occasionally in non–morphologically equal parts (asymmetrically).','Komárek et al. 2020',NULL,0,0),(2058,2337,'description','Cells solitary, without prominent mucilaginous envelopes, slightly elongated and oval, rounded at the ends, sometimes very slightly curved, with homogeneous, blue–green or greenish content, motile, with ± parietal, a little irregularly organized and waved thylakoids, without gas vesicles. The cells are connected rarely freely in short (few–celled) filamentous formations. Reproduction by cell binary fission in one plane, perpendicular to the longer axis of the cell.','Komárek at al. 2020',NULL,0,0),(2059,2337,'eco_distro','Planktic and in periphyton in watery localities in mineral springs, sometimes with higher content of salts, rarely also in the littoral of seas.','Komárek at al. 2020',NULL,0,0),(2060,2338,'description','planktic, periphytic, or metaphytic , solitary, slightly oval cyanobacterial cells with few parietal thylakoids and ± homogeneous content, 1.2–3.0 × 0.8–2.0 μm.','Komárek et al. 2020',NULL,0,0),(2061,2338,'etymology','pico = extremely small Synechococcus–like type from springs','Komárek et al. 2020',NULL,0,0),(2062,145,'description','Emended description: Cells solitary, lacking sheaths, without prominent gelatinous envelopes, but producing a thin layer of diffluent mucilage visible with staining by India ink, shortly oval to rod–shaped; cells occurring singly or in pairs, pale blue–green, with homogenous cell content (to 2–4 μm long), dividing by perpendicular symmetrical transverse binary fission, with few parietal photosynthetic thylakoids, not closely appressed to one another, with accessory pigments zeaxanthin and α–carotene.','Komárek et al. 2020',NULL,0,0),(2063,1618,'description','Emended description: Cells solitary, without enveloping sheaths, but with thin layer of diffluent mucilage, with homogenous pale blue–green cytoplasm, 0.4–2.4 μm long, 0.2–1.0 μm in diameter.<sup>​</sup>​​​​','Komárek et al. 2020',NULL,0,0),(2064,2339,'description','Genus showing typical <em>Chroococcus</em>-like morphology. At first spherical cells, solitary or in subcolonies of two to four cells, individually surrounded by a thick sheath. Later, cells hemispherical, irregularly arranged in aggregates of 4–16 cells, surrounded by a thin and colourless sheath; cell colour varying from yellowish, pale blue-green to olive green. Division by binary fission in three perpendicular planes; irregular fasciculated thylakoids. As of now, the genus occurs in soils. The most important criterion for establishment as new genus is the distinct 16S rRNA gene-based phylogenetic separation from <em>Chroococcus </em>sensu stricto.','Nowruzi &amp; Soares 2021',NULL,0,0),(2065,2339,'etymology','Al. bor\'zi.a. N.L. fem. n. Alborzia a genus named after Alborz, a mountain range in northern Iran','Nowruzi &amp; Soares 2021',NULL,0,0),(2066,2340,'etymology','the species was named after the Kermanshah province, Iran','Nowruzi &amp; Soares 2021',NULL,0,0),(2067,2340,'description','Unicellular, colonial, microscopical. On solid agar media, fast growing, forming green macroscopic colonies. On liquid culture medium, yellowish colonies at the bottom of the flask; slow growth. Cells at first subspherical, widely oval or spherical, 0.7–2.5 μm in diameter; pale blue-green; solitary or sometimes organized in spherical colonies of two to four cells (Fig. 2a), not densely packed together and never in rows or in regular arrangements. Cells individually surrounded by a conspicuous, thick and easily recognisable, lamellated sheath (Figs 2b and 3c, d). Later, cells hemispherical to spherical (Fig. 2c), olive green, rarely solitary, surrounded by a colourless, thin sheath (Fig. 2d), usually irregularly arranged in aggregates of 2–16 cells (Fig. 2e), up to 100 μm. In older cells, sheath is less recognisable or absent (Fig. 2f). Cell division by binary fission in three perpendicular planes (usually perpendicular to one another; irregularly in old colonies; Fig. 2g); cells do not reach the original shape before next division. Reproduction by cell division and by their liberation from colonies. Rarely nanocyte production. Fasciculated thylakoids are arranged irregularly throughout the cells (Fig. 3a). Presence of polyphosphate bodies.','Nowruzi &amp; Soares 2021',NULL,0,0),(2068,677,'etymology','ca.ver.ni co.la. L. n. caverna grotto; L. suff. -cola (from L. n. incola) inhabitant, dweller; N.L. n. cavernicola an inhabitant of a cavern','Roldán et al. 2013',NULL,0,0),(2069,676,'etymology','Cha.li.co.gloe9a. Gr. n. chalix chalk; Gr. n. gloios glutinous substance; N.L. fem. n. Chalicogloea glutinous substance growing on chalk','Roldán et al. 2013',NULL,0,0),(2070,2341,'description','Macroscopic colonies in natural habitat, as soft-textured mat-like entities as wild specimens, exhibit bluish green to dark bluish green appearance, only slightly mucilaginous, and can be picked up and separated easily from each other. On agar colonies start as blue-green filaments with irregular growth. No typical colony like appearance in plates with the irregular, multi-directional pattern of growth having more of mat-like appearance. All types of colonies that seem to appear have brittle appearance in plates. Thallus looks like an aggregation of irregularly arranged loose filaments with no prominent coiling. Cells have single plane of division. Sheath distinct, appearing all throughout the trichome. Sheath has colorless appearance. Exposure to sunlight also does not impart any kind of color to the sheath. Old cultures grown in nitrogendeficient medium (around 8 months) turn yellowish in liquid medium but again turn green after inoculation into fresh nitrogen-deficient medium. Signs of series of akinetes are also evident in very old cultures. Trichomes noticeably constricted at the cross-walls with the constrictions being evident in all stages of growth in any phase. Young 4–5 celled filaments occurring as hormogonia also present, but they usually appear rarely and trichomes are usually long. Cellular contents are usually granular. Vegetative cells are 3.5–4.5 um in length and 3.1–4.9 um in width, generally barrel shaped. Heterocytes are both intercalary and terminal, 4.7–5.5 um in length and 3.7–5.1 um in width, usually <s>​</s>spherical, though sometimes may also appear subspherical. Akinetes are rare, were not evident in any kind of series, perfectly oblong, much longer than the width, 6.5–8 um in length and 3.8–4.5 um in width.','Singh et al. 2016',NULL,0,0),(2071,2341,'etymology','The specific epithet ‘punensis’ is in honor of the city Pune, where this species was isolated.','Singh et al. 2016',NULL,0,0),(2072,2341,'diagnosis','Different from other closely related species due to the presence of a distinct sheath throughout the length of the trichome, significant difference in size and shape of the vegetative cells, heterocytes and the akinetes is found. Phylogenetic analyses using the 16S rRNA gene along with the rbcL, psbA, nifD genes and the PC-IGS operon gave a strong pattern of distinct clustering in case of all the molecular markers.','Singh et al. 2016',NULL,0,0),(2073,2343,'description','Found growing on soil as macroscopic mats with the presence of ample amount of water around the mats too; soft leathery texture in the natural habitat with sufficient light at the time of collection; color of mats is distinctly bluish green; laboratory-grown cultures appear proficiently as mats on plates retaining the bluish green of the natural sample in the initial stages of growth; prolonged growth in nitrogen-deficient media gradually makes the cultures turn yellowish and later brownish on the plates; gas vesicles evident: hormogonia formation also seen; thin hyaline sheath is present all around the filament with the sheath being evident even at the ends; prominently constricted cells; coiling of the filaments is average and overall the filaments are usually not entangled with each other; protoplasm appears clearly granular; vegetative cells almost barrel shaped to sometimes even appearing isodiametric; vegetative cells range in length from 3.6 to 4.0 μm while the width is around 3.2–3.7 μm; heterocytes are present at both the terminal and intercalary positions; heterocytes almost spherical in shape measuring about 3.8–4.3 μm in length to 3.7–4.9 μm in width; large sized spherical or oval akinetes prominently present; usually exhibit a prominent yellowish coloration.','Saraf et al. 2018',NULL,0,0),(2074,2343,'diagnosis','Phylogenetically and morphologically most similar to A. tiwarii from which it differs by having less wide &nbsp;vegetative cells. Differing fromA. morphoplasticum by having both wider vegetative cell and less oval heterocyte. Secondary structure of D1-D1’ helix region easily distinguishes A. soli from A. tiwarii and A. morphoplasticum. Strong phylogenetic support is evident for its distinct positioning and establishment as a new species of the genus Aliinostoc. Detailed morphological differences have been documented in Table 1.','Saraf et al. 2018',NULL,0,0),(2075,2343,'etymology','so’li. L. gen. n. soli of soil','Saraf et al. 2018',NULL,0,0),(2076,2344,'description','Growing like soft macroscopic mats in the natural habitat with easily visible greenish blue color; mats may range from 3 to 6 mm in diameter, usually soft texture when collected from the nature; on culturing in the laboratory, the filaments appear less coiled with more of a scattered view; filaments not entangled and not coalescent together; coiling is definitely not as dense as present in Nostoc; sheath present around the entire filament and appears more dense and thick in older cultures; presence of sheath is around the entire filament even at the ends<br>and around the terminal cells; gas vesicles seen; hormogonia formation clearly evident; loosely arranged &nbsp;filaments with variable tendencies for coiling; protoplasm appears clearly granular; cells almost barrel shaped to sometimes even appearing isodiametric; constriction prominent at the cross walls in between all the cells; cells prominently constricted at the cross walls; vegetative cells range in length from 5.3 to 5.6 μm while the width<br>is around 5.2–5.6 μm; heterocytes at both terminal and intercalary positions; heterocytes almost spherical in shape measuring about 3.8–4.3 μmin length to 3.7–4.9 μmin width; old decaying cells in chains in vegetative filaments also visible.','Saraf et al. 2018',NULL,0,0),(2077,2344,'diagnosis','Phylogenetically and morphologically most similar to A. soli, from which it differs by having distinctly wider cells. Differing from A. morphoplasticum by having both wider vegetative cells and less oval heterocyte. Differentiated from both species in the secondary structure of the D1-D1’ helix. Strong phylogenetic support is evident for its distinct positioning and establishment as a new species of the genus Aliinostoc. Detailed morphological differences have been documented in Table 1.','Saraf et al. 2018',NULL,0,0),(2078,2344,'etymology','ti.wa’ri.i. N.L. gen. n. tiwarii named in honor of Prof. D.N. Tiwari of the Department of Botany, Banaras Hindu University, India; a well-known researcher of cyanobacterial physiology and genetic studies along with being a hugely respected teacher','Saraf et al. 2018',NULL,0,0),(2079,2345,'description','Macroscopic amorphous colonies but not exactly mat like in the natural conditions; exhibit greenish color while the older colonies may start to appear dull green also; on being grown in the laboratory, the cultures appear light bluish in color; filaments are not very long and usually covered with thin transparent hyaline sheath all across the filament with the visibility being even at the ends; granular cytoplasm visible; cells appear prominently constricted; hormogonia formation is evident; vegetative cells appear almost barrel shaped or sometimes may even appear isodiametric; size of the vegetative cells may range from 4.0–4.5 μm in length to 4.1–4.7 μm in width; heterocytes prominently present at both terminal and intercalary positions; shape of the heterocytes may vary from being spherical to oblong; size of the heterocytes may range from 5.3–6.0 μm in length to 4.8–5.6 μm in width; akinetes distinctly visible with large size; irregular shape and dense protoplasmic contents at both terminal and intercalary positions; akinetes are also present just adjacent to the heterocyte.','Saraf et al. 2018',NULL,0,0),(2080,2345,'diagnosis','Morphologically differs from D. muscorum in having comparatively wider and longer vegetative cells. The heterocyte of D. magnisporum differs from D. muscorum in having longer and less wide heterocyte. The characteristic feature of this species is the presence of large sized and irregularly shaped akinetes at both the intercalary and terminal positions. Strong phylogenetic support is evident for its distinct positioning and establishment as a new species of the genus Desmonostoc. Detailed morphological differences have been documented in Table 1.','Saraf et al. 2018',NULL,0,0),(2081,2345,'etymology','mag.ni.spo’rum. L. adj. magnus large; Gr. n. spora, a seed and, in biology, a spore; N.L. neut. adj. magnisporum with large spores (akinetes)','Saraf et al. 2018',NULL,0,0),(2082,2346,'description','Filaments solitary, coiling or forming irregular bundles, surrounded by amorphous mucilage and overall usually not entangled. Sheaths colorless, hyaline, thin, sometimes thick, partially firm. Trichomes isopolar or curved, distinctly constricted at cross-walls. Vegetative cells barrel-shaped to spherical or cylindrical sometimes even appearing isodiametric. Heterocytes usually intercalary, rarely terminal. Intercalary heterocytes spherical to elliptical, terminal heterocytes subelliptical to oval. Akinetes spherical to elliptical or oval, intercalary, rarely large sized spherical akinetes present. Hormogonia with gas vesicles.','Lee et al. 2021',NULL,0,0),(2083,2346,'diagnosis','Pseudoaliinostoc shows close morphological resemblance to the genus Aliinostoc with almost no distinguishable differences being evident. But differs from other closely related Nostoc-like by 16S rRNA gene sequence (Fig. 2).','Lee et al. 2021',NULL,0,0),(2084,2349,'description','Filaments solitary or forming irregular bundles, surrounded by amorphous mucilage. Sheaths colorless, hyaline, thin, slightly thick, partially firm. Trichomes isopolar, straightly or curved, olive-green, distinctly constricted at cross-walls, 4.5–5.2 μm. Vegetative cells barrel-shaped, 2.9–5.3 μm long. Apical cells round, rounded-conical, sometimes narrower than vegetative cells. Heterocytes usually intercalary, rarely terminal. Intercalary heterocytes spherical to elliptical, 6.0–9.3×5.5–8.7 μm. Terminal heterocytes subelliptical to oval, 5.0–6.9×5.0–6.3 μm. Akinetes spherical to elliptical, intercalary, 6.8–7.7×7.2–8.3 μm. Hormogonia with gas vesicles.','Lee at al. 2021',NULL,0,0),(2085,2349,'etymology','sejongens, from Sejong Weir, the Republic of Korea','Lee at al. 2021',NULL,0,0),(2086,2350,'description','Macroscopic colonies in the form of dense greenish blue mats found near the base of a tree in a garden. Colonies appearing in nature as thick mats rather than exhibiting a discrete colony-like appearance. Mats having significant amount of mucilage around them and overall appearance showing the microhabitat having adequate amounts of moisture. Laboratory grown cultures having lightly coloured sheath around the entire trichome. Vegetative cells cylindrical to barrel shaped; usually with prominent constrictions between individual cells. Most of the cells are longer than the width and exhibit granular cytoplasm. Trichomes initially bright greenaish blue in colour but turn yellowish to brownish on prolonged growth. Filaments are usually not entangled and are loosely arranged with a slight tendency for coiling. Vegetative cells 3.2–9.5 μm in length to 2.4–4.0 μm in width. Heterocytes usually terminal; spherical to cylindrical; 3.0–10.2 μm in length to 3.2–5.5 μm in width. Akinetes large, prominently visible and are full of dense granular material. Akinetes may be in chains or solitary; generally oval though sometimes may also appear irregularly enlarged at one side; 3.4–11.3 μm in length to 3.3–6.4 μm in width.','Kabirnataj et al. 2020',NULL,0,0),(2087,2350,'etymology','catenatum ( ca. te. na\'tum. L. neut. adj. catenatum chained, because of the chained akinetes)','Kabirnataj et al. 2020',NULL,0,0),(2088,2351,'description','Macroscopic growth in the form of greenish blue discrete colonies found in a garden. Colonies appear very compact and have a comparatively tough mucilaginous texture. Trichomes also show the presence of lightly coloured sheath. Vegetative cells prominently constricted but not tapering at the ends; spherical to squarish or even cylindrical; 1.4–4.3 μm in length to 2.9–4.1 μm in width. Older cultures show lighter appearance and large numbers of disintegrated cells. Older filaments show a coiled appearance though young ones may be straight. Heterocytes terminal and intercalary; spherical though sometimes cylindrical at the terminal positions; 2.5–5.5 μm in length to 2.5–5.1 μm in width. Fragmentation between vegetative cells and heterocytes also seen. Hormogonia visible, both with and without heterocytes. Akinetes large; spherical and granular; 6.3–10.1 μm in length to 5.2–8.4 μm in width.','Kabirnataj et al. 2020',NULL,0,0),(2089,2351,'etymology','magnakinetifex ( magn. a. ki. ne\' ti. fex. L. masc. adj. magnus large; N.L. neut. n. akinetum akinete; L. suff. -fex (from L. v. facio to make) making; N.L. n. magnakinetifex the maker of large akinetes)','Kabirnataj et al. 2020',NULL,0,0),(2090,2352,'description','Macroscopic growth in the form of dark greenish mat in a paddy field filled with water. Mats appear rough in texture and have lot of colourless slimy mucilaginous material associated with them. Older mats on exposure to sunlight appear puffier, thicker and take up an almost dark greenish–brownish colour. Laboratory grown cultures exhibit typical dark bluish green colour and rough texture. Trichomes have mucilaginous sheath all around them and even at the ends. Vegetative cells appear granular with gas vesicles; usually barrel shaped to &nbsp;pherical/cylindrical with terminal cell slightly tapered; 2.5–6.5 μm in length to 3.1–5.6 μm in width. The cells are characteristically constricted at their ends, thus being the defining feature of this strain. Heterocytes prominently visible; terminal and intercalary; spherical to oblong with clear polar nodules; 6.5–8.0 μm in length to 3.0–6.8 μm in width. Akinetes were not observed.','Kabirnataj et al. 2020',NULL,0,0),(2091,2352,'etymology','constrictum ( con. stric\'tum. L. neut. past part. adj. constrictum constricted)','Kabirnataj et al. 2020',NULL,0,0),(2092,2353,'description','Macroscopic colonies in the form of dark bluish green mats collected from a paddy field having stagnant water; appear puffy and surrounded by large amounts of colourless mucilaginous material. The mats turn thicker and darker in colour on prolonged exposure to sunlight. Colourless sheath also surrounds the entire trichome even at the ends. Trichomes usually coiled and the vegetative cells are distinctly constricted between the ends; cytoplasm is also densely granular along with the presence of gas vesicles. Vegetative cells usually barrel shaped but sometimes may be wider than the length; terminal vegetative cells curved at the ends; 3.0–6.2 μm in length to 3.8–5.7 μm in width. Heterocytes intercalary and terminal; spherical or globose; polar nodules clearly visible; 6.0–7.9 μm in length to 5.5–7.2 μm in width. Akinetes were not observed.','Kabirnataj et al. 2020',NULL,0,0),(2093,2353,'etymology','constricta ( con. stric\'ta. L. fem. past part. adj. constricta constricted)','Kabirnataj et al. 2020',NULL,0,0),(2094,2354,'description','Macroscopic growth in the form of bluish green colonies growing as thick mats in paddy fields. At the time of collection the mats appear brightly coloured while they appear to loose colour later and become dull in appearance in later stages. The laboratory grown culture also appears bright bluish green and grows luxuriantly in nitrogen-deficient BG11 plates. The filaments appear long with slight tendency for coiling. Light coloured mucilaginous sheath surrounds all the amorphous colonies but is not truly mat like in the natural conditions; light mucilaginous sheath is also present all across the trichomes even at the ends. Vegetative cells barrel shaped to cylindrical; 1.9–5.5 μm in length and 2.2–5.4 μm in width; terminal vegetative cells curved at the ends. Heterocytes intercalary and terminal; intercalary heterocytes almost spherical with two polar nodules clearly visible; terminal heterocytes oblong and elongated at the ends with single polar nodule; 4.6–7.1 μm in length to 4.5–7.1 μm in width. Hormogonia formation also observed with the trichome having around nine vegetative cells and no heterocytes. Akinetes large; solitary; prominently intercalary; barrel shaped with length greater than width; 6.3–9.1 μm in length to 4.3–7.0 μm in width.','Kabirnataj et al. 2020',NULL,0,0),(2095,2354,'etymology','persicum (per\' si. cum. L. neut. adj. persicum, Persian, from Persia, the ancient Iran, referring to the place of origin of the type strain)','Kabirnataj et al. 2020',NULL,0,0),(2096,2356,'description','Filaments uniseriate and heteropolar with ovate-shaped terminal vegetative cell. Trichomes constricted at the cross-walls with prominent sheath covering throughout the length. Vegetative cells barrel-shaped to cylindrical with prominent granulation. Heterocytes usually terminal and rarely intercalary. 16S rRNA gene phylogenetic tree clearly separates Constrictifilum from the other phylogenetically related taxa.','Chavadar et al. 2021',NULL,0,0),(2097,2356,'etymology','<em>Constrictifilum </em>(Con.stric.ti.fi’lum. L. past. part. constrictus constricted, contracted; L. neut. n. <em>filum </em>a thread; N.L. neut. n. Constrictifilum a constricted thread)','Chavadar et al. 2021',NULL,0,0),(2098,2357,'description','Growing as a part of cyanobacterial/algal bloom formed in the water logged sugarcane field. In laboratory, the strain grows as discrete and irregular-shaped brownish colonies on solid media. Filaments uniseriate, heteropolar without hair formation and unbranched; straight or slightly curved. Sheath colorless; thin when young and thick in older filaments. Both the ends of the filament get defined at the early stages of the life cycle with heterocyte at one end and ovate-shaped terminal vegetative cell at the other end. Vegetative cells barrel-shaped to cylindrical without aerotopes. Terminal vegetative cells 6.11–9.49 μm long and 5.6–8.05 μm wide. Intercalary vegetative cells 4.11–8.21 μmlong and 5.98–8.28 μmwide. Heterocytes usually terminal; rarely intercalary. Terminal heterocytes are hemispherical, 6.13–9.71 μm long and 6.15–7.95 μm wide. Intercalary heterocytes are compressed hemispherical or cylindrical, 6.24–14.5 μm long and 6.4–9.6 μm wide. Formation of necridia followed by release of hormogonia with ovate-shaped terminal vegetative cell is the diagnostic feature of the species.','Chavadar et al. 2021',NULL,0,0),(2099,2357,'etymology','<em>karadense </em>(ka.da.den’se. N.L. neut. adj. <em>karadense </em>pertaining to Karad)','Chavadar et al. 2021',NULL,0,0),(2100,2358,'diagnosis','Differ from genera of Chroococcales, Chroococcidiopsidales, Nostocales, Oscillatoriales, Pleurocapsales, Spirulinales, and Synechococcales in lacking thylakoid membranes. Most similar to Gloeobacter in Gloeobacterales but lacks phycoerythrin.','Rahmatpour et al. 2021',NULL,0,0),(2101,2358,'etymology','An.tho.ce.ro.ti.bac’ter. N.L. masc. n. Anthoceros a genus of hornworts; N.L. masc. n. bacter a rod; N.L. masc. n. Anthocerotibacter a rod from hornworts.','Rahmatpour et al. 2021',NULL,0,0),(2102,2359,'description','The cells are rod-shaped, 0.5-1 um wide and 2-10 um long. Thylakoid membranes are absent. Carboxysomes are present, and polyphosphate granules often appear toward the cell poles. The major pigments are allophycocyanin, phycocyanin, and chlorophyll a. No phycoerythrin nor phycoerythrocyanin is present. Colonies are generally light to dark green in both liquid and solid BG11 medium, and never purple, orange, or brown like in Gloeobacter. Growth can occur under 10 - 100 umol photons m-2s-1 light intensities. No nitrogenase genes are present and cells do not grow without supplementing combined nitrogen. The type strain (C109) was originally isolated from a surface-sterilized hornwort <em>Leiosporoceros dussii</em> from Cocle, Panama (83° 7’34.6’’ N, 80°08’13.7’’ W). GC content of the type strain is 55.51%.','Rahmatpour et al. 2021',NULL,0,0),(2103,2359,'etymology','pa.na.men’sis. N.L. masc./fem. adj. panamensis, of or pertaining to Panama where the type strain was isolated.','Rahmatpour et al. 2021',NULL,0,0),(2104,2360,'description','Filaments entangled or loosely entangled, up to 1 mm long, with single-pored heterocytes at just one or both ends, unbranched. Sheath absent. Trichomes cylindrical, distinctly constricted at cross-walls. Cell content light green, blue-green to brownish blue-green, centroplasm and chromatoplasm sometimes distinguishable, granulated or with few prominent granules. Single-pored heterocytes usually isolated, sometimes in pairs, basal, variable in shape and size, conical-rounded, cylindrical-rounded to hemispherical or spherical. Two-pored heterocytes occasional to common, cylindrical, elliptical or nearly spherical. Akinetes rarely produced; when present, elliptical, single or in rows up to three akinetes, epispore thick, with striae.','Alvarenga et al. 2021',NULL,0,0),(2105,2360,'etymology','Amazonocrinis ( A. ma. zo. no. cri´nis. Gr. fem. pl. n. Amazones, the Amazones; L. masc. n. crinis, lock of hair; N.L. masc. n. Amazonocrinis an Amazonian lock of hair; referring to the Amazon rainforest, from where the type strain was isolated).','Alvarenga et al. 2021',NULL,0,0),(2106,2361,'etymology','Amazonocrinis nigriterrae ( ni. gri. ter´rae. L. masc. adj. niger, black; L. fem. n. terra, earth; N.L. fem. n. nigriterrae of black earth; referring to the soil from which its type strain was isolated).','Alvarenga et al. 2021',NULL,0,0),(2107,2361,'description','Filaments loosely entangled, flexuous, longer than 600 μm, usually with single-pored heterocytes at just one end, occasionally at both ends, unbranched. Sheath absent. Trichomes cylindrical, distinctly constricted at cross-walls. Cells 2.9–5.3 μm long (4.0 μm average), 2.4–3.1 μm diam. (2.7 μm average), length:diameter ratio from 1.0 to 2.1 (1.5 μm average). Cell content light green, blue-green to brownish blue-green, centroplasm and chromatoplasm sometimes distinguishable, with few prominent granules. Single-pored heterocytes usually isolated, basal, variable in shape and size, conical-rounded or cylindrical-rounded, 3.7–4.9 μm long (4.3 μm average), 3.1–3.9 μm diam. at the larger axis (3.4 μm average). Two-pored heterocytes frequent, cylindrical or elliptical, 4.3–5.8 μm long (5.0 μm average), 3.2–4.9 μm diam. at the larger axis (3.9 μm average). Akinetes not observed.','Alvarenga et al. 2021',NULL,0,0),(2108,2362,'etymology','Atlanticothrix ( At. lan. ti´ co. thrix. Gr. masc. adj. atlantikos, Atlantic; Gr. fem. n. thrix, hair; N.L. fem. n. Atlanticothrix Atlantic hair; a filament from the Atlantic Forest, in reference to where the type strain of this filamentous cyanobacterium was isolated from).','Alvarenga et al. 2021',NULL,0,0),(2109,2362,'description','Filaments in groups or interwoven, unbranched, up to 500 μm long, sometimes forming extensive mats, occasionally isolate cells among filaments, commonly with single-pored heterocytes at just one end, unbranched. Sheath sometimes present, thin, hyaline, but mostly absent. Trichomes cylindrical, distinctly constricted at cross-walls. Cell content light blue-green, brownish green or reddish, centroplasm and chromatoplasm usually indistinguishable, granulated (sometimes with just one or several prominent granules). Vegetative cells barrel-shaped. Single-pored heterocytes usually isolated, basal, variable in shape and size, conical-rounded to spherical. Akinetes elliptical, epispore not evident. Heterocyte germination common.','Alvarenga et al. 2021',NULL,0,0),(2110,2363,'etymology','Atlanticothrix silvestris ( sil. ves´tris. L. fem. adj. silvestris, related to the forest; in reference to the type strain being isolated from samples collected in a forest).','Alvarenga et al. 2021',NULL,0,0),(2111,2363,'description','Filaments in groups, short, up to 300 μm long, commonly with single-pored heterocytes at just one end, unbranched. Sheath sometimes present, thin, hyaline, but mostly absent. Trichomes cylindrical, distinctly constricted at cross-walls. Vegetative cells barrel-shaped, 1.0–3.0 μm long (1.4 μm average), 1.7–3.6 μm diam. (2.3 μm average), length:diameter ratio from 0.4 to 1.5 (0.8 μm average). Cell content light blue-green, brownish green or reddish, centroplasm and chromatoplasm usually indistinguishable, granulated (sometimes with just one prominent granule). Single-pored heterocytes usually isolated, basal, variable in shape and size, conical-rounded to spherical, 1.6–3.1 (–2.4) μm long, 1.8–2.9 (–2.2) μm diam. at the larger axis. Two-pored heterocytes occasional, cylindrical to spherical, 1.5–2.7 (–2.1) μm long, 2.0–2.8 (–2.3) μm diam. at the larger axis. Akinetes elliptical, 2.3–4.1 (–3.3) μm long, 2.1–3.1 (–2.7) μm diam. at the larger axis, epispore not evident. Heterocyte germination common.','Alvarenga et al. 2021',NULL,0,0),(2112,2364,'etymology','Dendronalium ( Den. tro. na´lium. Gr. neut. n. dendron, tree; N.L. neut. n. Dendronalium, an organism found in trees; a reference to most of the strains having been isolated from tree samples).','Alvarenga et al. 2021',NULL,0,0),(2113,2364,'description','Filaments entangled or tightly interwoven, up to 200 μm long, occasionally arranged in parallel, occasionally circinate, usually with single-pored heterocytes at just one end, occasionally at both ends, unbranched. Sheath sometimes present, thin, hyaline. Trichomes cylindrical, distinctly constricted at cross-walls. Cell content blue-green, brownish green, reddish green or light green, centroplasm and chromatoplasm sometimes distinguishable, granulated (sometimes with one or several prominent granules). Cells cylindrical, barrel-shaped<br>or rounded, sometimes elliptical. Single-pored heterocytes usually isolated, sometimes in pairs, basal, variable in shape and size, conical-rounded to spherical. Two-pored heterocytes common, cylindrical to spherical. Akinetes cylindrical rounded to elliptical, in irregular rows with up to eight akinetes, epispore hyaline, smooth, but not always evident. Heterocyte germination common.','Alvarenga et al. 2021',NULL,0,0),(2114,2365,'etymology','Dendronalium phyllosphericum ( phyl. lo. sphe´ ri. cum. Gr. neut. n. phyllon, leaf; L. fem. n. sphaera, sphere; L. neut. suff. -icum, related to; N.L. neut. n. phyllosphericum, related to the phyllosphere; referring to most of the isolated strains having been obtained from leaf samples).','Alvarenga et al. 2021',NULL,0,0),(2115,2365,'description','Filaments tightly interwoven, occasionally arranged in parallel, occasionally circinate, up to 200 μm long, with single-pored heterocytes at just one or at both ends, unbranched. Sheath sometimes present, thin, hyaline. Trichomes cylindrical, distinctly constricted at cross-walls. Cells cylindrical, barrel-shaped or rounded, 1.4–4.0 μm long (2.7 μm average), 1.3–2.6 μm diam. at the larger axis (1.9 μm average), length:diameter ratio from 0.8 to 2.5 (1.4 μm average). Cell content brownish green, reddish green or light green, centroplasm and chromatoplasm sometimes distinguishable, granulated (sometimes with one or several prominent granules). Single-pored heterocytes usually isolated, sometimes in pairs, basal, variable in shape and size, conical-rounded to nearly spherical, 1.2–4.2 μm long, 1.6–2.7 μm diam. at the larger axis. Two-pored heterocytes cylindrical, 2.0–5.0 μm long, 1.9–3.1 μm diam. at the larger axis. Akinetes cylindrical rounded to elliptical, 3.0–5.0 μm long, 2.9–3.9 μm diam. at the larger axis, epispore hyaline, smooth. Heterocyte germination common.','Alvarenga et al. 2021',NULL,0,0),(2116,191,'diagnosis','Emended diagnosis: Forms mat-like structures in liquid cultures that easily disintegrate into single, rounded aggregates of one millimeter. Rarely solitary cells, mostly micro- or macroscopic, irregular, formless, or granular colonies, composed of densely, irregularly aggregated cells or their small groups, surrounded by mucilaginous envelopes. Cells subspherical, more or less irregular rounded in outline, sometimes slightly elongate (never spherical or ellipsoidal) enveloped by thin, narrow, and clearly delimited, sometimes diffluent toward outer periphery, sometimes feebly lamellate, and sometimes colored sheaths, usually following the cell outline. Tetrads sometimes present; nanospores were not observed. Cell division is irregularly in various planes in successive generations. Reproduction by liberation of divided end ensheathed cells from ruptured mother sheaths. The occasional presence of enlarged resting cells with thick, firm, and usually intensely colored envelopes can be observed.<br><em>Gloeocapsopsis </em>differs from other coccoid cyanobacterial genera by their dense but not squeezed aggregation of cells that have an irregularly rounded but never spherical or elongated form surrounded by a firm envelope.','Jung et al. 2021',NULL,0,0),(2117,2366,'diagnosis','Emended diagnosis: Cells aggregating, up to macroscopic clumps or mats of a few millimeters, gelatinous, irregular, olive-green to blue-green when young. Cells irregular-spherical, (2.5) 4–8 μm in diameter, with thin, colorless, limited, and non-lamellate sheath; outer envelopes hyaline, diffluent. Cell content is vivid olive green<br>or slightly blue-grayish, usually homogeneous, not granulated. Tetrad formation present and nanospores absent; Reproduction by liberation of divided end ensheathed cells from ruptured mother sheaths. The parietal thylakoid position is visible in light microscopy.','Jung et al. 2021',NULL,0,0),(2118,2367,'description','Unicellular, spherical cells, 2.4(±0.2) μm × 2.2(±0.3) μm and 3.3(±0.4) μm in diameter, often angularly clinched, and heterogeneous in size during colony development (Figures 2, 4, and 5; Supplementary Tables 1 and 2). Cell content is homogeneous, non-granulated, green to olive green, and never blue, with parietal thylakoid membranes and thylakoid-free nucleoplasm in the center. The sheath of single cells is always colorless, slightly lamellate, and limited with up to 1 μm thickness. Binary fission of mother cells leads to division in different directions, without nanocytes. Cells often agglomerated into irregular packets of two or more cells, often forming tetrads, surrounded by a common firm, limited, sometimes slightly lamellate, and colorless sheath. Older colonies can be observed as two types: (1) packages containing small, geometrically clinched cells embedded together in a common colorless, limited, and firm sheath forming a rounded pattern; (2) tetrad-like packages with cells unitedly clinched in packages of only a few cells that are agglomerated densely with other packages of about the same size, held together by a colorless sheath that firmly mimics the shape of the cell packages.','Jung et al. 2021',NULL,0,0),(2119,2367,'etymology','‘<em>dulcis</em>’ – ‘sweet’, due to the high contents of trehalose and sucrose that the species accumulates when confronting desiccation','Jung et al. 2021',NULL,0,0),(2120,2368,'description','Unicellular, spherical cells, 3.2(±0.2) μm × 2.4(±0.2) μm, 4.0(±0.3) μm in diameter, and more or less uniform throughout colony development (Figures 2, 7, 8; Supplementary Tables 1 and 2). Cell content is homogeneous, non-granulated, olive green, and sometimes bluish, with parietal thylakoid membranes and thylakoid-free nucleoplasma in its center. Single cells always show colorless, non-lamellate, and limited sheaths of up to 1 μm thickness. Binary fission of mother cells leads to division in different planes, without nanocytes. the irregular arrangement, surrounded by an irregular sheath with varying electron density. Cell divisions were observable<br>by the formation of a septum (Figures 8B,D, arrows), which gave rise to the formation of colonies. Recently divided cells stayed in the sheath of the thin mother cell (Figure 8C). The central nucleoplasm was free of thylakoids and contained medium electron-dense carboxysomes, clearly detected by their polygonal shape (Figures 8B,C). The electron density of the carboxysomes varied (Figure 8E). Other electron-dense granules were determined as cyanophycin granules due to their round appearance and their radiating pattern (Figure 8C).<br>Thylakoids showed a parietal arrangement (Figure 8C), and during septum formation were pushed inward<br>(Figure 8D). At a higher magnification, distinct electrondense phycobilisomes were clearly visible on thylakoid<br>membranes (Figure 8E). Cells in colonies were surrounded by a thin cell wall (Figure 8C) and embedded in a somewhat multi-layered sheath with varying electron densities from electron dense (Figure 8D) to loose and apparently disintegrating (Figure 8F, arrow).','Jung et al. 2021',NULL,0,0),(2121,2368,'etymology','‘<em>diffluens</em>’ – ‘diffluent’, because of the diffluent gelatinous sheath of older colonies that release single unsheathed cells.','Jung et al. 2021',NULL,0,0),(2122,2369,'diagnosis','Thallus blue–green, fine, smooth and diffluent, forming biofilms. Filaments solitary, straight or slightly waved, flexuous. Trichomes motile, cylindrical, very slightly constricted at the cross walls, not attenuated towards the ends, sometimes with thin and colorless sheath, containing only one trichome. Cells cylindrical, elongated up to 4 times (rarely isodiametric), (1.6)3.2–5.0(6.9) μmlong and 1.2–2.8(4.0) μmwide and cyanophycin granules at the cross-walls. Apical cell rounded, without calyptra, polar gas vacuoles are absent. Thylakoid arrangement is parietal.','Samylina et al. 2021',NULL,0,0),(2123,2369,'etymology','Baaleninema = The name of the genus refers to the name of Professor Dr Chase van Baalen (1925–1986), an American microbiologist who was the first who studied strain PCC7105 and deposited it to the Pasteur Culture Collection and to the filamentous morphology (Greek word νμα, or n´ıma means ‘filament’).','Samylina et al. 2021',NULL,0,0),(2124,2370,'diagnosis','Thallus attached to substrates and forming biofilms. Trichomes straight, very slightly constricted at the cross walls, not attenuated towards the ends, sheath absent or thin and colorless, contain only one trichome. Highly motile. Cells cylindrical, elongated, (1.6)1.9–4.8(6.9) μm long and 1.2–2.8 μm wide and cyanophycin granules at the cross-walls. Apical cell rounded, without calyptra, polar gas vacuoles are absent. Thylakoid arrangement is parietal.','Samylina et al. 2021',NULL,0,0),(2125,1639,'diagnosis','Thallus emerald green, diffluent, forming thin mats or freefloating filaments. Filaments solitary or parallel in bundles, nearly straight, flexuous, blue–green, pale blue–green or yellow–green. Trichomes motile, cylindrical, slightly constricted at the cross walls, slightly attenuated towards the ends, sheaths are absent or thin and colorless, containing only one trichome. Bundles of trichomes can be surrounded by amorphous, colorless slime. Cells cylindrical, isodiametric or elongated, (2.3)2.6–5.7 μm long and 2.0–4.6 μm wide. Cross-walls with 1–2 cyanophycin granules on either or both sides and/or with yellowish granulations with homogeneous or finely granular content. Apical cells rounded, hemispherical, sometimes with extrusions, often with a large polar gas vacuole. Thylakoid arrangement is parietal with a central fascicle, sometimes with spherical formations. Possess nifH genes of ‘desulfo’ type.','Samylina et al. 2021',NULL,0,0),(2126,1639,'eco_distro','The taxon occurs in saline–alkaline and soda lakes and marine and mixosaline to hypersaline inland environments.','Samylina et al. 2021',NULL,0,0),(2127,2371,'etymology','The specific epithet (orleanskyi) named in honor of Dr Vladimir K. Orleansky, a Russian algologist who worked in theWinogradsky Institute of Microbiology of Russian Academy of Sciences.','Samylina et al. 2021',NULL,0,0),(2128,2371,'description','Thallus blue–green, diffluent, forming biofilms or free-floating solitary filaments. Trichomes blue–green or pale blue–green, motile, cylindrical nearly straight, flexuous, slightly attenuated towards the ends and very slightly constricted at cross-walls. Sheath thin and colorless, contain only one trichome. Cells cylindrical, elongated (2.9–5.0 × 2.1–2.7 μm). Granulations at cross-walls are yellowish with homogeneous or finely granular content. Apical cell rounded, hemispherical, often with a large polar gas vacuole. Thylakoid arrangement is parietal with a central fascicle. Differs significantly from other Sodalinema species in the length and structure of the V2 helix of the 16S–23S ITS region and geography (Africa).','Samylina et al. 2021',NULL,0,0),(2129,2372,'etymology','The specific epithet (gerasimenkoae) is named in memory of the prominent microbiologist and cyanobacterial specialist Dr Lyudmila M. Gerasimenko who worked in the Winogradsky Institute of Microbiology of Russian Academy of Sciences and isolated the type strain of the species.','Samylina et al. 2021',NULL,0,0),(2130,2372,'description','Thallus blue–green, diffluent, forming biofilms or free-floating solitary filaments. Trichomes motile, cylindrical nearly straight, flexuous, slightly attenuated towards the ends and very slightly constricted at cross-walls. Sheath thin and colorless, contain only one trichome. Cells cylindrical, isodiametric or elongated ((2.3)3.0–4.6(5.0) × (2.2)3.0–4.6 μm). Cross-walls with a refractive granule on either or both sides coupled with minor yellowish granulations with homogeneous or finely granular content. Apical cell rounded, hemispherical, often with a large polar gas vacuole. Thylakoid arrangement is parietal with a central fascicle. Differs significantly from other Sodalinema species in the structure of the V2 helix of the 16S–23S ITS region, geography (Asia) and ecology.','Samylina et al. 2021',NULL,0,0),(2131,2373,'description','Thallus blue–green, diffluent, forming biofilms or free-floating solitary filaments. Trichomes motile, cylindrical nearly straight, flexuous, slightly attenuated towards the ends and very slightly constricted at cross-walls. Sheath thin and colorless, contain only one trichome. Cells cylindrical, elongated (2.6–4.8(5.5) × 2.0–3.3(3.5) μm). A refractive granule on either or both sides of the cross walls can be present. Apical cell rounded, &nbsp;sometimes with extrusions, often with a large polar gas vacuole. Thylakoid arrangement is parietal with a central fascicle. Differs significantly from other Sodalinema species in the structure of the V2 helix of the 16S–23S ITS region, geography (Europe) and ecology (halophilic).','Samylina et al. 2021',NULL,0,0),(2132,2373,'etymology','The specific epithet (stali) named in honor of Professor Dr. Lucas J. Stal, an outstanding microbiologist known for his long-term research in the field of cyanobacterial ecology and who isolated the type strain of the species.','Samylina et al. 2021',NULL,0,0),(2133,2374,'diagnosis','Similar to many Calothrix species differ from those by presence of multiple short, isopolar/heteropolar hormogonia encapsulated within a single sheath. Forms independent clade from any established Dulcicalothrix spp., based on 16S rRNA, rbcL and rpoC1 phylogenies. Additionally, different from type species of Dulcicalothrix in ITS sequence.','Nowruzi et Shalygin 2021',NULL,0,0),(2134,2374,'description','In natural populations, form dark green or blackish spots on the surface of the submerged paddles. In cultures, form similar colonies on the agar surface. Filaments from short to long, more or less straight or wavy, usually with transparent, hyaline sheaths. Occasionally single collars observed in the middle part of the filaments. Sheaths tightly adherent to the edges of the cells, sometimes widened or onion–like swollen, always colorless. Trichomes, 7.0–7.5 μm wide at the middle, up to 8 μm wide at the base. Single–, double–false, and geminate branching frequent. Trichomes gradually taper to the conical cells, without formation of the hairs, sometimes onion–like swollen in the base (8 μm), 7.0–7.5 μm wide at the middle. Cells grey–green, granulated, of different shapes, mostly discoid 7.5 × 3–4 μm, sometimes without constrictions. Heterocytes single or two in the row, basal or intercalary, of different shapes and sizes: hemispherical or half–rounded, 6 × 8 μm, rounded, 4.5 μm or oblong 7.5 × 4–6 μm. Necridia present.','Nowruzi et Shalygin 2021',NULL,0,0),(2135,2374,'etymology','Alborzica. Adj. from Alborz, the name of a mountain range in northern Iran from where this species was isolated.','Nowruzi et Shalygin 2021',NULL,0,0),(2136,2375,'description','Colonies spherical, start yellow green, and become to gray green. Filaments released by the colony rupture, covered with or without sheath, and the filaments densely entangled to form young colony. Within the colony, the filaments segmented into several small groups, and the small groups showing compartmentalization of mucilage, later to form small spherical colony. Consequently, the older colony consist of aggregations of microcolonies, just like a beehive. Eventually the older colony broken to release these small colonies. Sheath thick, colorless. Vegetative cells short barrel shaped to subspherical, or oblong, 2.7–3.1–3.8 μm long and 2.7–4.4–4.6 μm wide. Heterocytes subspherical, with a diameter of 2.8–4.3–4.9 μm. Akinetes not observed during years of cultivation.','Cai et al. 2021',NULL,0,0),(2137,2375,'etymology','favosum = “favose”, refers to typical morphological characteristics of this species','Cai et al. 2021',NULL,0,0),(2138,2376,'description','Thallus macroscopic in nature and in culture. In culture, forming macroscopic masses on test tube bottom in liquid media. On agar, macroscopic colonies, as aggregation of spherical colonies with distinct mucilage, which remain distinct throughout the whole life cycle. Macrocolonies dark green. Filaments with no sheath released from the colony, and later form distinct, colorless sheath, and terminal heterocyte outside of the sheath. Then the trichomes irregular, tightly entangled in the sheath, to form young long filamentous colony, the heterocytes appeared at the end of the colony. The sheath outside of the colony, shrank to separate the filamentous colony into smaller colonies. Later these smaller colonies connected by heterocyte, and eventually formed spherical colonies. Vegetative cells elliptic or spherical, 2.8–3.4–3.7 μm long and 3.0–3.5–3.9 μm wide. Heterocytes larger than vegetative cells, short barrel shaped that protrude from the population, subspherical within the colony. 3.3–3.9–4.2 μm long, 3.6–4.1–4.8 μm wide. Akinetes not observed during years of cultivation.','Cai et al. 2021',NULL,0,0),(2139,2376,'etymology','<em>mirabile</em>, referring to unique morphological characteristics of this species','Cai et al. 2021',NULL,0,0),(2140,2377,'description','Trichomes solitary or forming small colony (mats) in culture. Cells blue-green. Trichomes straight or slightly curved, few- or multi-celled. Facultative sheaths thin, colorless. Cells cylindrical, rounded slightly barrelshaped, 1.57–5.99 (8) μm long and 1.04–1.87 (2.19) μm wide. Cells clearly constricted at cross-walls, connected with hyaline bridges, content homogeneous. Terminal cells cylindrical or conical or rounded. Thylakoids parietal. Reproduction by one-celled to multi-celled hormogonia without necridic cells.','Kim et al. 2021',NULL,0,0),(2141,2377,'diagnosis','Vegetative cells of Pinocchia daecheonga facultatively has no polar aerotope (Table 1). The ultrastructure observed by TEM showed parietal arrangement of the thylakoids like the order Synechococcales (Fig. 3). It differed from the already-known <em>Pinocchia polymorpha</em> Dvořák, Jahodářová et Hašler (Dvořák et al. 2015) and other close relatives (e.g., <em>Leptoelongatus litoralis</em> Chakraborty et Mukherjee (Chakraborty et al. 2019) and <em>Leptothoe spongobia </em>Konstantinou &amp; Gkelis (Konstantinou et al. 2019) by 16S rRNA gene sequences (species in Fig. 4).','Kim et al. 2021',NULL,0,0),(2142,2377,'etymology','daecheonga, from the Daecheong lake in Korea','Kim et al. 2021',NULL,0,0),(2143,2378,'description','The cell morphology of the A183 strain indicated by light microscopy revealed straight, wavy, and occasionally bent trichomes (Figure 1A). The SEM and TEM (Figures 1B–D) showed that trichomes of strain A183 were unbranched and composed of 80–120 elongated barrel-shaped cells, 1.30–1.60 um in length and 1.05–1.10 um in width. Constrictions were observed at the cross-walls of cells (Figures 1B–D). Individual cells of the filaments were divided by centripetal invagination of the cell wall (Figure 1E). Intracellular connections between vegetative cells were not observed (Figure 1D). The TEM analysis also exhibited that the three to five thylakoid layers were located in parallel at the inner periphery of cells (Figures 1C,D) and can be described as parietal according to recent classification (Mareš et al., 2019). Sheath, septum, phycobilisome, carboxysomes, cyanophycin granule, and polyphosphate bodies were present in the cytoplasm (Figures 1C–F), and small lipid droplets were also observed (Figure 1C).','Tang et al. 2021',NULL,0,0),(2144,2378,'etymology','Species epithet derives from the name of collection site.','Tang et al. 2021',NULL,0,0),(2145,460,'description','Filaments forming expanded blue-green mats on the substratum and large floating membranaceous aggregates in older liquid cultures. With LM, variously curved, flexuous, densely packed, isopolar trichomes, with rounded apical cells. Each trichome individually surrounded by a thin colorless sheath. Cells longer than wide (1.2–3 lm long and 0.8–1 lm wide) with distinct constrictions at the cross walls. Homogeneous cell content and lack of gas vesicles. Reproduction by trichome fragmentation into short hormogonia without necridia. Cell division always symmetrical, perpendicular to the longitudinal axis of the trichome, and daughter cells dividing and growing to the size of the mother cell before the next division. Slow gliding motility on solid medium. With TEM, 3–4 parietal thylakoids and a multilayered sheath approximately 0.15 lm thick. Water-soluble pigments: allophycocyanin, C-phycocyanin (the most abundant), and phycoerythrin. Lipidsoluble pigments: two different myxoxanthophylls (sensu Karsten and Garcia-Pichel, 1996), isozeaxanthin, zeaxanthin, chlorophyll a, echinenone and b-carotene. Typical of thermal environments, usually growing on thermal muds.','Sciuto &amp; Moro 2016',NULL,0,0),(2146,460,'diagnosis','detected by molecular and phylogenetic analyses based on the 16S rRNA gene and 16S–23S ITS region. 16S–23S ITS region with distinctive boxB and V3 helices','Sciuto &amp; Moro 2016',NULL,0,0),(2147,460,'etymology','the specific epithet ‘‘<em>albertanoae</em>” (fem. gen.) was given in the honor of the phycologist Patrizia Albertano, who devoted a great part of her research career to the study of Leptolyngbyaceae and who gave a precious contribution to the first paper on strain ETS-08 (i.e., Moro et al., 2010)','Sciuto &amp; Moro 2016',NULL,0,0),(2148,2379,'diagnosis','detected by molecular and phylogenetic analyses based on the 16S rRNA gene and 16S–23S ITS region. 16S–23S ITS region with distinctive boxB and V3 helices','Sciuto &amp; Moro 2016',NULL,0,0),(2149,2379,'description','Filaments forming expanded blue-green mats on the substratum and large floating membranaceous aggregates in older liquid cultures. With LM, variously curved, flexuous, isopolar trichomes, with rounded apical cells. Each trichome individually surrounded by a thin colorless sheath. Cells longer than wide (2–6.5 um long and 0.8–1.8 lm wide) with distinct constrictions at the cross walls. Homogeneous cell content. Reproduction by trichome fragmentation into short hormogonia without necridia. Cell division always symmetrical, perpendicular to the longitudinal axis of the trichome, and daughter cells dividing and growing to the size of the mother cell before the next division. Slow gliding motility on solid medium. With TEM, 4–6 parietal thylakoids and unlayered sheath. Water-soluble pigments: allophycocyanin, C-phycocyanin, and phycoerythrin. Lipid-soluble pigments: one myxoxanthophyll (sensu Karsten and Garcia-Pichel, 1996), isozeaxanthin, zeaxanthin, chlorophyll a, echinenone and b-carotene. Typical of thermal environments.','Sciuto &amp; Moro 2016',NULL,0,0),(2150,2379,'etymology','the specific epithet ‘‘oregonensis” (fem. adj.) refers to the country of the type locality','Sciuto &amp; Moro 2016',NULL,0,0),(2151,2380,'description','Thallus in form of dark isopolar filaments with ability to form distinct mats. Sheaths facultatively present, colorless, sometimes lamellated, with only one trichome present in a single sheath, false branching not present. Trichomes gently tapering toward both ends; unbranched; not or only slightly constricted at the cross walls; color ranging from pale greyish green to golden brown and purple. Several last cells of the trichome often yellowish. Cells always distinctly shorter than wide, actual length depending on the phase of division. New cell walls often formed before the previous one is finished, making parts of the trichome reminiscent of a ruler. Small granules often located at the cross walls. Apical cells rounded, calyptra occasionally present. Necridia and hormogonia frequent. Trichomes movement by gliding. Division of cells exclusively cross-wise, reproduction by the disintegration of trichomes.','Hauerová et al. 2021',NULL,0,0),(2152,2380,'etymology','From the latin word <em>tenebris </em>– dark; referring to the conspicuously dark color of filaments when creating visible biomass.','Hauerová et al. 2021',NULL,0,0),(2153,2381,'description','Thallus in form of dark filaments creeping on substrate. Filaments up to 33 μm wide. Sheaths facultatively present, colorless, sometimes lamellated, only one trichome present in a sheath. Trichomes 14–24 μm wide, gently tapering toward the ends, (10) 12–20 μm wide at the end; unbranched; not or only slightly constricted at the cross walls; color ranging from golden brown to purple. Several last cells of the trichome often yellowish. Cells distinctly shorter than wide, 1.5–6 μm long depending on the phase of division. New cell wall often formed before the previous one finished, making parts of the trichome reminiscent of a ruler. Small granules often located at the cross walls. Apical cells rounded, calyptra occasionally present. Necridia and hormogonia frequent. Trichomes gliding.<br><strong>Ultrastructural notes</strong>: The granulation is often located at the crosswalls and the ends of the trichomes can be terminated by a prominent calyptra (Fig. 3 B).','Hauerová et al. 2021',NULL,0,0),(2154,2381,'etymology','From latin word <em>amphibius </em>referring to both freshwater and terrestrial origin of studied strains','Hauerová et al. 2021',NULL,0,0),(2155,2383,'description','Thallus in form of dark filaments creeping on substrate, eventually forming dark mats that can be released to float on water surface. Filaments 18–25 μm wide. Sheaths facultatively present, colorless, thin, only one trichome present in a sheath. Trichomes 10–17 μm wide, gently tapering toward the ends, 9–12 μm wide at the end; unbranched; not or only slightly constricted at the cross walls; straight or loosely spirally-coiled or hooked at the ends; color ranging from pale greyish green to brownish and purple. Several last cells of the trichome<br>often yellowish. Cells distinctly shorter than wide, 2–5 μm long depending on the phase of division. New cell wall often formed before the previous one finished, making parts of the trichome reminiscent of a ruler. Small granules often located at the cross walls. Apical cells rounded, calyptra occasionally present. Necridia and hormogonia frequent. Trichomes gliding.','Hauerová et al. 2021',NULL,0,0),(2156,2384,'description','Thallus blue-green, growth pattern appears like fascicles or bundles rather than forming a mat-like biofilm. Filaments isopolar, uniseriate, unbranched, cells slightly longer than their width, cell length ranged from 1.4 - 2.1 μm and width 0.9 - 1.1 μm. Cross walls have distinct constrictions. Trichomes were cylindrical, immotile, no heterocyte or akinete. Small sized filaments known as hormogonia helps in propagation. Necridic cells present. Ultrastructure includes parietal thylakoids, aerotopes present.','Chakraborty et al. 2021',NULL,0,0),(2157,2384,'etymology','The specific epithet ‘<em>pallustris</em>’ represents the swampy habitat of the strain from where it was collected.','Chakraborty et al. 2021',NULL,0,0),(2158,2385,'description','Thallus blue-green, growth like fascicles or bundles. Filaments isopolar, uniseriate, unbranched, cells slightly longer than their width, cell length ranged from 1.4 - 2.1 μm and width 0.9 - 1.1 μm. Cross walls have distinct constrictions.','Chakraborty et al. 2021',NULL,0,0),(2159,2385,'etymology','The generic epithet “Aerofilum” is derived from Aero Greek for ‘air’ as the strain possesses gas vesicles (aerotopes) and filum Greek for ‘filament’.','Chakraborty et al. 2021',NULL,0,0),(2160,2386,'description','Thallus blue-green, growth pattern appears like fascicles or bundles rather than forming a mat-like biofilm. Filaments isopolar, uniseriate, unbranched, cells slightly longer than their width, cell length ranged from 1.4 - 2.1 μm and width 0.9 - 1.1 μm. Cross walls have distinct constrictions. Trichomes were cylindrical, immotile, no heterocyte or akinete. Small sized filaments known as hormogonia helps in propagation. Necridic cells present. Ultrastructure includes parietal thylakoids, aerotopes present.','Chakraborty et al. 2021',NULL,0,0),(2161,2386,'etymology','The specific epithet ‘<em>fasciculatum</em>’ reflects the growth pattern of the strain appearing to grow as a cluster or fascicles instead of forming a mat-like biofilm.','Chakraborty et al. 2021',NULL,0,0),(2162,2387,'diagnosis','Akin to <em>Stanieria </em>by morphology, different from which by marine habitat, epi-endophytic growth on the rhodophyte <em>A. vermiculophyllum</em>, and based on 16S rRNA gene phylogeny.','Bonthond et al. 2021',NULL,0,0),(2163,2387,'description','In culture, small groups of cells forming blackish visible aggregates (macrocolonies). Microcolonies consist of mostly individual, spherical cells; or oblate-spherical cells in groups growing together. Cells in the microcolony of different sizes, terracotta or pale grey-brown by color. Cells surrounded by thin, colorless mucilaginous envelopes, never with common slime. Baeocytes formation through multiple fission of the mature cells, which are much larger than baeocytes. Baeocytes are released by cell wall breakage. Reproduction exclusively by baeocyte production.','Bonthond et al. 2021',NULL,0,0),(2164,2387,'etymology','Named in honour of John B. Waterbury—an important cyanobacterial researcher, who worked on morphology and physiology of many marine baeocyte producers.','Bonthond et al. 2021',NULL,0,0),(2165,2388,'description','Macrocolonies slowly growing in liquid BG11 medium (20 PSU) under low light conditions in form of tight blackish clusters. Microcolonies small, consisting of released baeocytes (3.5–6 lm in diameter), growing baeocytes (up to 8 lm in diameter), and large, mature cells ready to form baeocytes through multiple fission (7–20 lm in diameter). Mucilaginous envelopes colorless, adherent to the cell walls, rarely slightly widened and more robust especially in the stressed cultures. Released baeocytes growing to large sizes (up to 19–20 lm), after which multiple fission occurs. Sometimes baeocytes form in the smaller mother cells, 10–15 lm. Growing cells spherical or oblate-spherical, terracotta by color, released baeocytes pale grey-brown. Unreleased baeocytes abundant, 64 or 128 per one mother cell; small, 2–2.5(3) in diameter.','Bonthond et al. 2021',NULL,0,0),(2166,2388,'diagnosis','Morphologically similar to <em>Stanieria sublitoralis</em>, but differing by phylogenetic position on the 16S rRNA gene tree and by being associated with <em>Agarophyton vermiculophyllum</em>. Akin to <em>Chroococcopsis gigantea</em>, different by 16S rRNA gene phylogeny, smaller cells, lacking daughter cells and its distribution in marine to brackish habitats.','Bonthond et al. 2021',NULL,0,0),(2167,2388,'etymology','<em>Agarophyton</em>- from the marine red alga <em>Agarophyton vermiculophyllum</em> (Ohmi) Gurgel et al., and -<em>cola</em> from L. n. <em>incola</em>; an inhabitant.','Bonthond et al. 2021',NULL,0,0),(2168,2389,'diagnosis','Growing in benthic habitat, similar to typical Chroococcus in morphology, but morphologically differing with tightly arranged colonial cells and often staggered and arranged asymmetrically pairs of cells in common colonies; molecularly differing in 16S rRNA gene sequence phylogeny and similarity (&lt;94.5%), and ITS secondary structures.','Wang et al. 2021',NULL,0,0),(2169,2389,'description','Colonies microscopic, loosely stacked, usually 2–8-celled, rarely solitary cells. Solitary cells with large cell volume ≥4-celled colonies. Mucilage surrounding individual cells and colonies; mucilaginous envelopes clearly delimited, form, not stratified or diffluent, colorless. Individual cells rarely spherical (only in solitary cells), subspherical or hemispherical in colonies, homogeneous, darkgreen, olive-green, green when young, yellowish when old. Thylakoids irregularly arranged. Cell division in three planes by binary fission, without nanocytes or baeocytes.','Wang et al. 2021',NULL,0,0),(2170,2389,'etymology','<em>Crypto </em>(Gr.) = hidden; <em>chroococcus </em>(L.) = genus <em>Chroococcus</em>; a hidden subgenus of the genus <em>Chroococcus</em>.','Wang et al. 2021',NULL,0,0),(2171,2390,'diagnosis','Not floating; morphologically differing from Chroococcus-associated taxa with tightly arranged colonial cells and often staggered and arranged asymmetrically pairs of cells in common colonies; phylogenetically forming a unique clade from other Chroococcus-associated taxa; low similarity (94.5%) of 16S rRNA gene sequences compared with other cyanobacterial taxa and unique secondary structures of the ITS region.','Wang et al. 2021',NULL,0,0),(2172,2390,'description','In liquid culture, microscopic colonies or macroscopic dark-green mats loosely stacked on the bottom of glass test tubes (Fig. 1G). Colonies usually 2–8-celled, rarely solitary cells, 11.05–21.91 um wide in 2–4-celled colonies. Solitary cells with large cell volume, ≥4-celled colonies. Mucilage surrounding individual cells and colonies, mucilaginous envelopes clearly delimited, firm, not stratified or diffluent, colorless, 1–2 um wide. Colonial cells tightly arranged as pairs of cells in common colonies, often staggered and arranged asymmetrically. Individual cells rarely spherical (only in solitary cells), subspherical, or hemispherical in colonies, 4.57–11.13 um, homogeneous, olive-green and green when young (Fig. 1, A–E), granulated, and yellowish when old (Fig. 1F). In old cultures, deformed and shrunken dead cells are sometimes stained by red material of the surrounding reddish bacterial groups (Fig. 1, J–L). Thylakoids are irregularly arranged (Fig. 2, A–F). Cell division occurs in three irregular planes by binary fission, without nanocytes or baeocytes.','Wang et al. 2021',NULL,0,0),(2173,2390,'etymology','Named for the original site of collection for the type strain, Tibet, China.','Wang et al. 2021',NULL,0,0),(2174,2391,'diagnosis','Planktonic, morphologically corresponding to genus <em>Limnococcus </em>(specifically the former Chroococcus limneticus) in the variable mucilage and diverse cellular morphology, differing from type species <em>L. limneticus</em> by the clearly delimited and lamellated mucilage, and ultrastructurally by the loose and dense irregular thylakoid arrangements as well; phylogenetically close to L. limneticus and distant from Merismopediaceae; differing from other Chroococcus-associated taxa by predicted short D1– D1 &nbsp;stems in secondary structures of the ITS region.','Wang et al. 2021',NULL,0,0),(2175,2391,'description','In liquid culture, microscopic, free-floating, dispersed, usually 2–4-celled, rarely 8-celled, often solitary cells. Individual cells subspherical or hemispherical in colonies. Solitary cells often large in volume, spherical, oval, kidney shaped or elongated when fresh (Fig. 3, A–D), variously shaped when old (Fig. 3, E–I). Colonies or individual cells 8.43–21.45 um in diameter. Mucilage surrounding individual cells and colonies, clearly<br>delimited, lamellated (Fig. 3 arrows in B, D and F; Fig. 2 arrows in G and I), colorless, sometimes detaching in culture and increasing the viscosity of the culture. Cells homogenous, olive-green, bluegreen when young, granulated, and yellowish when old (Fig. 3, D and I). Thylakoids irregularly arranged, with both loose and dense segments (Fig. 2, G–L). Cell division in three planes by irregular or regular binary fission, without nanocytes or<br>baeocytes.','Wang et al. 2021',NULL,0,0),(2176,2391,'other','<em>fonticola </em>(L.) = an inhabitant of a fountain','Wang et al. 2021',NULL,0,0),(2177,2392,'description','Coccoid cyanobacteria olive green-, brown-, violet-, or dark green-colored in liquid culture or in colonies on agar. Cell division in two successive planes at right angle; daughter cells single or paired, rarely in tetrads, shapeless aggregates occasionally produced. Sheath and capsule absent; a small amount of mucilage present. Thylakoids are stacked in 4–6 peripheral layers. Freshwater, nonhalotolerant cyanobacteria. Palmitic and a-linolenic acids predominate. Phycoerythrin produced, and able to complementary chromatic adaptation. In one of the species, chl d and chl f produced under far-red light.','Averina et al. 2021',NULL,0,0),(2178,2392,'etymology','Similar to Synechocystis in morphology and ultrastructure, but differs as follows: (i) belongs to the freshwater non-halotolerant ecotype; (ii) contains palmitate and a-linoleate as major fatty acids; (iii) is able to complementary chromatic adaptation, chl d and f are produced in one of the species under far-red light; (iv) is distinct in the 16S rRNA, rpoC1, and rbcL genes from Synechocystis spp.; and (v) is distinct from Synechocystis spp. in the 16S-23S ITS region sequence and folding.','Averina et al. 2021',NULL,0,0),(2179,2392,'etymology','Altericista (L. fem. n. Al.te.ri.cis ta. L. masc. adj. alter another; Gr. n. kiste/L. n. cista a box; Altericista another box-shaped cell).','Averina et al. 2021',NULL,0,0),(2180,2393,'description','Olive green- or brown-colored coccoid cyanobacteria 2.0  0.2 um long (min., 1.3 um; max., 2.9 um) and 1.8  0.2 um wide (min., 1.2 um; max., 2.3 um); single, in pairs, rarely in tetrads, occasionally in shapeless aggregates. Sheath or capsule absent; thylakoids stacked in 4–6 peripheral layers. Loose precipitate is produced in unstirred liquid culture; growth in stirred culture occurs at a rate of ~0.2–0.4  d<sup>-1</sup>. Surface colonies rounded, with slightly wavy edge, moderately folded and granular, bordered with slime. Freshwater, nonhalotolerant cyanobacteria (suppressed by ~1% addition of sodium chloride to the modified BG-11 medium containing 0.05% of total salt). Type-III chromatic adaptation is observed. Nucleotide sequence of 16S rRNA gene is &lt;98% similar to those in other species of the genus; distinct in nucleotide sequences of the B-Box and V3 domains of the 16S-23S ITS region (the B-Box domain, also in folding).','Averina et al. 2021',NULL,0,0),(2181,2393,'etymology','A. lacusladogae: (L. masc. adj. la.-cus.la do.gae. L. masc. nom. lacus a lake, lacusladogae, of Lake Ladoga (Northwest Russia), the largest freshwater lake in Europe.','Averina et al. 2021',NULL,0,0),(2182,2394,'description','Violet-colored coccoid cyanobacteria 1.7  0.2 um long (1.3 um, min.; 2.0 um, max.) and 1.5  0.1 um wide (0.9 um, min.; 1.8 um, max.). Cell aggregation, ultrastructure, cultural characteristics, ecotype, and salt response as in the type strain <em>A. lacusladogae</em> CALU 1127. Phycoerythrin-rich cyanobacteria; type-II chromatic adaptation is observed. Nucleotide sequence of 16S rRNA gene is &lt;98% similar to those in other species of the genus; distinct in nucleotide sequences of the B-Box and V3 domains of the 16S-23S ITS region (the B-Box domain, also in folding).','Averina et al. 2021',NULL,0,0),(2183,2394,'etymology','A. violacea: (L. fem. adj. vi.o.la ce.a. L. fem. adj. violacea, violet-colored).','Averina et al. 2021',NULL,0,0),(2184,2395,'description','Dark green-colored coccoid cyanobacteria 2.0  0.2 um long (min., 1.6 um; max., 2.6 um) and 1.8  0.2 um wide (1.4 um, min.; 2.3 um, max.). Cell aggregation, ultrastructure, cultural characteristics, ecotype, and salt response as in the type strain <em>Altericista lacusladogae</em> CALU 1127. Type-III and type-VI chromatic adaptations are observed; accessory chl d and chl f produced in farred light. Nucleotide sequence of 16S rRNA gene is &lt;98% similar to those in other species of the genus; distinct in nucleotide sequences of the B-Box, D-D0 domain, and V3 domains of the 16S-23S ITS region (the B-Box and D-D’ domains, also in folding).','Averina et al. 2021',NULL,0,0),(2185,2395,'etymology','Altericista variichlora: (L. fem. adj. va.ri.i.-chlo ra. L. masc. adj. varius different, Gr. masc. adj. chloros/L. n. chloris green; variichlora possessing different chlorophylls).','Averina et al. 2021',NULL,0,0),(2186,2396,'description','Cells solitary, more commonly irregular or in rounded colonies with many cells (up to 32–64 or more), usually aggregated irregularly, extended (Fig. 1 A–C). Mucilage unstratified, colorless and firm, surrounding cells and colonies. Cells cylindrical 1.6–6.87 μm long, 1.17–5.85 μm wide, 1 to 1.75 × longer than wide (mean, 1.28 ×) (Fig. 1 C–D). Cells easily squeezing from colonies with pressure (Fig. 1 C). The chromatoplasm and centroplasm usually recognizable with light microscopy (Fig. 1 C–D). Cell contents blue-green, slightly granulated, or sometimes homogeneous. Reproduction by simple binary cell division in three or more planes.','Abdullin et al. 2021',NULL,0,0),(2187,2396,'etymology','The species epithet ‘vladivostokensis’ is derived from the type locality Vladivostok City.<sub>​</sub>','Abdullin et al. 2021',NULL,0,0),(2188,2397,'description','Filaments straight or flexuous, mostly bright blue-green or green; no branching, immotile; sheath colorless, sometimes indistinct under the LM; no heterocytes or other special cells present. Trichomes solitary, cylindrical, &lt;3 μm wide, and slightly constricted at the cross-walls. Cells mostly isodiametric or slightly longer than wide, usually with pale-to-shiny granules located at cross-walls; no aerotopes. Terminal cells rounded, without calyptra, and morphologically similar to other cells. Reproduction by trichome fragmentation.','Rasouli-Dogaheh et al. 2022',NULL,0,0),(2189,2397,'etymology','Thai (ไทย) refers to Thailand—country of origin of the type species,—nema (νήμα)—thread (Gr.), refers to appearance of the organism.','Rasouli-Dogaheh et al. 2022',NULL,0,0),(2190,2398,'description','Colony pale to bright blue-green. Filaments, 1–3 μm wide. Trichomes mostly straight and slightly constricted, or not constricted at the cross-walls. One trichome present in a sheath with no branching, but the presence of sheaths for some filaments could not be determined with certainty under the LM. Cells longer than wide (2–3.5 μm long), mostly isodiametric (1.5–2 μm long) with pale yellowish-to-golden granules. Reproduction by trichome fragmentation. Aerotopes absent. Terminal cells typically rounded, without calyptra. Necridic cells absent (Fig 6). TEM micrographs demonstrated definite presence of sheaths. Parietal thylakoids (4–5 per cell) were visible in the longitudinal section but were less discernable in the cross-section. Cyanophycin granules were observed among thylakoids. Apical cells were rounded. The cell wall was simple like that of most species in the Leptolyngbyaceae family.','Rasouli-Dogaheh et al. 2022',NULL,0,0),(2191,2398,'diagnosis','According to a recent taxonomic classification [9], Thainema salinarum differs from Halomicronema excentricum morphologically in terms of cell size and the lack of gliding motility and gas vesicles.','Rasouli-Dogaheh et al. 2022',NULL,0,0),(2192,2398,'etymology','Name of the species refers to the original habitat of the material.','Rasouli-Dogaheh et al. 2022',NULL,0,0),(2193,2399,'description','Colonies microscopic, multicellular, epilithic, composed of small groups of irregularly arranged cells (Fig. 3A), enveloped by wide, individual gelatinous envelopes, joined together into a formless mass (Fig. 3B). Cells and their groups always surrounded by wide gelatinous sheaths. Cells always spherical, olive blue-green or brown content.','Panou &amp; Gkelis 2022',NULL,0,0),(2194,2399,'etymology','The name comes from the Greek word Σπηλαιώτης, meaning the one who lives in caves.','Panou &amp; Gkelis 2022',NULL,0,0),(2195,2400,'description','Colonies micro- or macroscopic, irregular, gelatinous, dirty greyish brown composed of spherical or cubic-like subcolonies, 15–75 μm in diameter (Fig. 3A, Table S4). Subcolonies with 4–16 cells, surrounded by individual delimited, more or less wide, usually distinctly lamellate, pale envelopes. Outer sheaths usually pale, almost colourless. Cells dirty brown-green, spherical or slightly elongate after and before division, 6–8 μm in diameter (Fig. 3B, Table S4).','Panou &amp; Gkelis 2022',NULL,0,0),(2196,2400,'etymology','The specific epithet refers to the anchialine ecosystems, the habitat of the species; from the Greek word ἀγχίαλος meaning close to the sea.','Panou &amp; Gkelis 2022',NULL,0,0),(2197,2401,'description','Colonies microscopic, multicellular, subsphericalirregular with densely aggregated cells (Fig. 3E), enveloped by thin, usually firm, colourless envelopes in dense sarcinoid packets forming of macroscopic irregular mats. Cells spherical, subspherical, oval, hemispherical, enveloped by thin mucilaginous sheaths, usually packed closely to one another (Fig. 3D).','Panou &amp; Gkelis 2022',NULL,0,0),(2198,2401,'etymology','The Genus name derives from the Greek word ἁλίπλαγκτος meaning the one surrounded by the sea, the sea-wanderer or sea-roaming.','Panou &amp; Gkelis 2022',NULL,0,0),(2199,2402,'description','Colonies microscopic, containing 2–32 cells, 12 × 12 μm in diameter (Table S4), or composed of many-celled colonies, arranged packet-like aggregates with thin colourless mucilaginous envelopes (Fig. 3 D-E, Table S4); thallus pale greyish. Cells more or less spherical, after division hemispherical, 2–3 μm in diameter, pale blue<br>green.','Panou &amp; Gkelis 2022',NULL,0,0),(2200,2402,'etymology','The specific epithet refers to Anthony Quinn Bay in Rhodes Island, Greece, the species type locality, a beach named after the famous actor Anthony Quinn.','Panou &amp; Gkelis 2022',NULL,0,0),(2201,2403,'description','Thallus thin, delicate, mostly bright brown–red, diffluent, sometimes fascicle-like, usually forming thin mats (Fig. 5A); rarely isolated trichomes. Sheaths absent. Trichomes ± parallel-arranged, cylindrical, straight, slightly flexuous, not constricted at the cross-walls, bent and spherically capitate at the ends (Fig. 5C) motile, with intense gliding in the direction of the longitudinal axis, sometimes accompanied by a distinctive rotation.','Panou &amp; Gkelis 2022',NULL,0,0),(2202,2403,'etymology','The genus name Olisthonema is made up of the Greek words ὀλισθαίνω (olisthaín¯o) - slide and νῆμα (nema)-filament.','Panou &amp; Gkelis 2022',NULL,0,0),(2203,2404,'description','Colony (thallus) spreading, with bundles of filaments, sometimes forming coils, bright red to brown (Fig. 5 A-B). Trichomes up to 1 mm long, intensely motile, slightly bent and entangled, slightly constricted at the distinct cross-walls, 2–2.3 μm wide. Cells 2–4 × longer than wide, brown red, with translucent, sometimes reddish, granules at the cross-walls (Fig. 5C), (3)3.5–8 μm long (Table S4). The main diacritic feature is morphology of trichomes without sheaths and particularly the shape of the end cells, which are in developed stages attenuated and elongated, narrowed, bent, spherically capitate, up to 15 μm long (Fig. 5C). Contains PE.','Panou &amp; Gkelis 2022',NULL,0,0),(2204,2404,'etymology','The specific epithet refers to Estonia (Eesti in Estonian) where the strain was isolated from.','Panou &amp; Gkelis 2022',NULL,0,0),(2205,2405,'description','Filamentous cyanobacteria, forming green and black compact subaerophytic biofilms (Fig. 5H) on solid substrata. Filaments fine, long and wavy. Young filaments appear to be more or less straight. Sheaths thin, firm, colourless, attached to the trichomes, sometimes widened at the ends. Trichomes cylindrical, not constricted at cross walls, sometimes slightly constricted toward the end (Fig. 5I, Table S4). Cells isodiametric, slightly shorter than wide or longer than wide with green or blue-green content. Reproduction occurs via formation of<br>hormogonia, produced by fragmentation of trichomes, often by means of irregular necridic cells (Fig. 5H).','Panou &amp; Gkelis 2022',NULL,0,0),(2206,2405,'etymology','The Genus name comes from the Greek word σπέος, meaning cave.','Panou &amp; Gkelis 2022',NULL,0,0),(2207,2406,'description','Filaments with a single trichome per sheath. Sheath colourless, firm, thin (Fig. 5I). Trichomes occasionally slightly attenuated toward their ends (Fig. 5I). Trichome fragmentation via the random occurrence of necridic cells within a filament (Fig. 5H). Cells variable in shape, mostly isodiametric, sometimes slightly shorter or longer than wide. Cell size 2.8–5.1 μm long, 3.3–4.1 μm wide (Table S4). Cell contents homogenous, may occasionally appear grainy. Necridic cells sometimes present. Apical cell rounded. Filaments grow preferentially in dimly lit areas. Sheaths in apical cell appear to be enlarged, more or less rounded detached from the cell (Fig. 5I).','Panou &amp; Gkelis 2022',NULL,0,0),(2208,2406,'etymology','This name is in tribute to Pavlos Fyssas (1979–2013) a Greek musician and activist, murdered by a member of the criminal organization Golden Dawn.','Panou &amp; Gkelis 2022',NULL,0,0),(2209,2407,'description','Macrocolonies in form of thin, blue-green film growing on agar surface. Filaments long, occasionally coiled or slightly waved (Fig. 5D), with or without sheath, 1.8–2 (4.5) μm wide (Table S4). Mucilaginous sheaths colorless, soft, hyaline to firm and persistent beyond the apex of the trichome, rarely slightly swollen, clearly visible as wider than the trichome, in older stages mostly firm (Fig. 5F). Trichomes distinctly constricted at the cross-walls, granulated mostly in the older stages, 1.5–2 μm wide forming nodules (Fig. 5E). Cells bright bluegreen when young, pale green when old, from isodiametric to elongate, 1.5–2.5 (4) μm long, rarely with polar granules (Table S4). Apical cells rounded to slightly conical, elongated up to 4.5 μm long. Reproduction occur with hormogonia with the formation of necridic cells (Fig. 5F). Contains PC.','Panou &amp; Gkelis 2022',NULL,0,0),(2210,2407,'etymology','This name is in tribute to Ioannis D. Pantis (1957–2017), a Greek university professor of Ecology, whose pioneering work contributed greatly to environmental protection and ecosystem management, including coastal areas, in Greece.','Panou &amp; Gkelis 2022',NULL,0,0),(2211,2408,'description','Thallus at first bright blue-green, becoming a darker duller blue-green with age, and consisting of many subspherical colonies or aggregations of filaments enclosed in a common mucilage, up to 1 cm long. Colonies with compact aggregations of cells (Fig. 9A), at first with filamentous arrangement not visible, later released within a few days of transfer to fresh media (Fig. 9C), motile, 3 μm wide. Filaments at first uniseriate (Fig. 9B), later multiseriate (Fig. 9C), up to 10 μm wide. Vegetative cells in hormogonia quadratic, isodiametric to longer than wide, 3.4–4.6 μm long, becoming spherical or compressed subspherical in mature filaments, dividing in more than one plane, 4.1–6.2 μm in diameter (Table S4). Heterocytes developing in germinating akinetes<br>2–3 μm in diameter, later 3–5.3 μm in diameter. Akinetes 3.5–6 μm in diameter (Table S4).','Panou &amp; Gkelis 2022',NULL,0,0),(2212,2408,'etymology','The specific epithet comes from the Greek word Хίος (Chios) referring to the island located in the Aegean Sea, Greece.','Panou &amp; Gkelis 2022',NULL,0,0),(2213,2409,'description','Macroscopic growth in the form of dark greenish mat in rocks in the shore of a brackish lake. Mats appear rough in texture and have lot of colourless slimy mucilaginous material associated with them (Fig. 9D). Older mats on exposure to sunlight appear puffier, thicker and take up an almost light brownish colour (Fig. 9E). Laboratory grown cultures exhibit typical light brownish colour, dark blue-green in younger stages (Fig. 9F). Trichomes have mucilaginous sheath all around them and even at the ends. Vegetative cells appear granular with gas vesicles; usually barrel shaped to spherical/cylindrical with terminal &nbsp;cell slightly tapered; 2.5–6.5 μm in length to 3.1–5.6 μm in width (Table S4). Trichomes irregular waived to coiled (Fig. 9F), cells are characteristically constricted at their ends (Fig. 9F), thus being the defining feature of this strain. Heterocytes prominently visible; terminal and intercalary; spherical to oblong with clear polar nodules; 6.5–8.0 μm in length to 3.0–6.8 μm in width. Akinetes were not observed.','Panou &amp; Gkelis 2022',NULL,0,0),(2214,2409,'etymology','The specific epithet derives from the greek word ὑφάλμυρος, meaning brackish.','Panou &amp; Gkelis 2022',NULL,0,0),(2215,2410,'description','Strain growing in benthic mats in shallow brackish lake. Filaments in small clusters or mats on the substrate, more or less straight, 6–8.2 μm wide (Table S4). Trichomes cylindrical, constricted at the cross-walls (Fig. 9G); sheaths sometimes slightly layered, distinct, but fine, diffluent and colourless, up to 1 μm wide. Terminal cells shortly barrel-shaped, always without gas vesicles, blue-green, sometimes with small granules, terminal cells in young trichomes often conical (Fig. 9G). Heterocytes, 3.6–3.9 μm length and 3.6–9.1 μm wide, shortly barrelshaped or ± rounded when terminal. Sheaths in terminal heterocytes enlarged and rounded (Fig. 5H). Akinetes more or less compressed or rounded, up to 2–4 in series (Fig. 9I) (Table S4). Rounded sheath in terminal heterocyte and akinetes in series are the main diacritic features of the species. Contains PC.','Panou &amp; Gkelis 2022',NULL,0,0),(2216,2410,'etymology','The specific epithet comes from the from Late Latin Mediterraneum mare (Mediterranean Sea).','Panou &amp; Gkelis 2022',NULL,0,0),(2217,2411,'description','Thallus in tufts forming woolly mats (Fig. 7E), dark brown, epilithic growing in dark mats on rocks in terrestrial caves. Sheaths firm, attached to trichomes, not lamellated. Filaments truebranched, only with T-brancing (Fig. 7A). Trichomes uniseriate, ± isopolar, with cells shorter or longer than wide, often enlarged near heterocytes. Cells with different forms across a trichome, barrel-shaped, cylindrical, slightly and/or distinctly constricted (Fig. 7A-C). Heterocytes intercalary barrel shaped and terminal with conical form (Fig. 7B, 8D, and 8F). Cells and heterocytes contain polar granules, up to one and three polar granules respectively (Fig. 7D).','Panou &amp; Gkelis 2022',NULL,0,0),(2218,2411,'etymology','The genus name comes from the ancient Greek name Ἰφιάνασσα, one of the three maenadic daughters of Argive Proetus that inhabited a cave after going mad.','Panou &amp; Gkelis 2022',NULL,0,0),(2219,2412,'description','Thallus woolly (Fig. 7E), partly growing subaerophytically with densely coiled and/or parallel-arranged filaments. Filaments long, isopolar, very slightly attenuated towards the ends (Fig. 7D). Sometimes heteropolar young filaments are obvious germinating from hormogonia with a basal heterocyte. Filaments truebranched with a T-like type of branching (Fig. 7A), T-type of branching originating from the oblique division of an intercalary cell (Fig. 7C). Cell before branching often enlarged and forming a type of nodule (Fig. 7C). Heterocytes intercalary, 5.2–10.7 μm (8.15 μm ± 1.63, n = 30) wide and 6.7–15 μm (9.62 μm ± 2.85, n = 30) long with a pale yellow content (Table S4). Mature filaments 7.8–12 μm (9.55 μm ± 0.99, n = 30) wide. Branches narrower than the main filament, 4.84–8.1 μm (6.58 μm ± 0.91) wide. Sheath thin and firm, colorless. Trichomes constricted at the cross walls and extending slightly attenuated at the ends. Cells cylindrical or dolichoform to barrel-shaped, 5.16–13 μm (8.2 μm ± 1.9, n = 30) long at the mature filaments, and 8.17–15.6 μm (10.98 μm ± 2.34, n = 30) long at the young filaments, with smooth finely granulated content, blue-green to brownish, macroscopically violet (Fig. 7A, 8F) (Table S4). End cells more or less rounded (Fig. 7D). Ensheathed hormogonia (Fig. 7D). Strain in grown cultures form young woolly mats, later joined in larger ones moving to top of the culture, with a part of the mat growing subaerophytically on top of the liquid media (Fig S3 A-B). Necridic cells sometimes present (Fig. 7D).','Panou &amp; Gkelis 2022',NULL,0,0),(2220,2412,'etymology','The specific epithet is in tribute to Zaharias (Zak) Kostopoulos (1985–2018) a Greek LGBTQI + and HIV activist, and drag queen, known also as Zackie Oh.','Panou &amp; Gkelis 2022',NULL,0,0),(2221,2413,'description','Homocytous, uniseriate, isopolar, straight to slightly curved to coiled, filamentous. Thalli planktonic and/or attached to substrata and vegetation, prostrate, erect, fascicular or not. Euryhaline. Filaments with or without sheaths. Trichomes with or without constriction at cross wall. Cell content granulated typically at cross-walls. Cells discoid, apical cells range from bluntly rounded, to conical rounded, to rounded, calyptra present or not. Reproduction by single cell release, hormogonia, and/or diagonal fragmentation. False branching is rare. Currently, this family includes the genera <em>Affixifilum, Capilliphycus, Limnoraphis, Limnospira, Neolyngbya, Sirenicapillaria</em> and <em>Tigrinifilum</em>, which differ by 16S rRNA phylogeny.','Berthold et al. 2022',NULL,0,0),(2222,2413,'diagnosis','Monophyletic group of marine/brackish/freshwater genera based on the 16S rRNA gene phylogeny, sister to the Laspinemataceae clade.','Berthold et al. 2022',NULL,0,0),(2223,2413,'etymology','Name based on the genus <em>Sirenicapillaria</em>, a rigid marine filamentous cyanobacterium that forms nuisance benthic blooms across the Florida western and southern coasts.','Berthold et al. 2022',NULL,0,0),(2224,2414,'description','Homocytous filamentous cyanobacteria, forming dark brown, blue green erect thallus on benthos. Long coarse filaments (c. 10 cm) with thick, sometimes facultative and lamellate hyaline sheath. Trichomes cylindrical, thicker in the centre and slowly attenuated towards apices, uniseriate, constricted at cross-walls. Cells discoid, shorter than wide. Cell content light to dark brown, greyish green and blue green. Apical cell rounded, narrowed at times, with occasional calyptra. Reproduction by release of individual cells, straight or diagonal trichome fragmentation, necridia, hormogonia. Rarely false branches.','Berthold et al. 2022',NULL,0,0),(2225,2414,'etymology','From Latin Siren (Greek Σειρήν), a Siren, and Latin capillus, hair, in reference to the long thalli and ‘mermaid’s hair’ appearance of these marine cyanobacteria.','Berthold et al. 2022',NULL,0,0),(2226,2415,'description','Thallus erect, light to dark blue green. Filaments straight and somewhat flexuous, longer than 10 cm, 18.4–25.2(–28) μm wide with thick hyaline sheath. Trichomes cylindrical, (14–)15–20(–21) μm wide,<br>thicker in the centre and gradually attenuated towards the ends. Cells slightly constricted at cross walls. Cells discoid, wider than long, 1.3–2.8 μm long. Cell content light to dark green, blue green to greyish, with<br>lightly pigmented cells towards apices. Apical cell rounded, at times conical, with occasional calyptra. Reproduction by straight or diagonal trichome fragmentation, hormogonia, and necridia.','Berthold et al. 2022',NULL,0,0),(2227,2415,'etymology','Latin adjective glaucus, -a, -um, in reference to the ‘sea green’ cell and thalli colour of this cyanobacterium.','Berthold et al. 2022',NULL,0,0),(2228,2416,'description','Thallus dark brown, tangled, web-like. Filaments straight and rigid, 5 cm long, 28–83(–94) μm wide with thick, lamellate hyaline sheath. Trichomes cylindrical, 22.8–63.3 μm wide, thicker in the middle and gradually attenuated towards apices. Cells slightly constricted at cross walls. Cells discoid, wider than long, 1.8–3.9 μm long. Cell content light to dark brown, with pigmentless cells towards apices. Apical cell rounded, at times conical, with occasional calyptra. Reproduction by release of individual cells, straight or diagonal trichome fragmentation, necridia, hormogonia.','Berthold et al. 2022',NULL,0,0),(2229,2416,'etymology','Latin adjective rigidus, -a, -um, in reference to the physical rigidity of the filaments.','Berthold et al. 2022',NULL,0,0),(2230,2417,'description','Thallus erect, light to dark brown, almost black. Filaments straight and flexuous, 5 cm long, 12.5–33(–35) μm wide with thick hyaline sheath. Trichomes cylindrical, 10–26.8 μm wide, thicker in the centre and gradually attenuated towards apices. Cells slightly constricted at cross walls. Cells discoid, wider than long, 1.0–2.4 μm long. Cell content light to dark brown, grey to red, with pigmentless cells towards apices. Apical cell rounded, at times conical, with occasional calyptra. Reproduction by straight or diagonal trichome fragmentation, hormogonia and necridia. Rarely false branches.','Berthold et al. 2022',NULL,0,0),(2231,2417,'etymology','The epithet stauglerae is in honour of Elizabeth ‘Betty’ Staugler for her committed work in studying and surveying coastal marine habitats and the ‘Eyes on Seagrass’ Florida Sea Grant Extension programme, which first noted the emergence of this cyanobacterium blanketing areas that had previously been inhabited by seagrasses.','Berthold et al. 2022',NULL,0,0),(2232,2418,'description','Homocytous filamentous cyanobacteria forming solitary and free-floating, straight, wavy to slightly flexuous filaments, with or without thin hyaline sheath. Trichomes cylindrical. Cells slightly constricted between meristematic zones, highly constricted between dividing cells in older filaments. Cross-walls densely granulated and darkened except at the filament ends. Cells discoid, wider than long. Cell content light to dark green, blue green, brown, and grey. Apical cell rounded, with occasional clear calyptra. Reproduction by fragmentation or hormogonia.','Berthold et al. 2022',NULL,0,0),(2233,2418,'etymology','From Latin tigrinus, striped like a tiger, and Latin filum, a thread, in reference to the resemblance of a ‘banded tiger’ characteristic of the filaments.','Berthold et al. 2022',NULL,0,0),(2234,2419,'description','Filaments solitary and free-floating, or attached to substrate. Filaments straight, wavy, to flexuous, (9–)10.2–19 μm wide with thick hyaline sheath. Trichomes cylindrical, (7–)8.0–19.2 μm wide. Cells slightly constricted between meristematic zones, highly constricted between dividing cells in older filaments. Cross-walls densely granulated and darkened. Cells discoid, wider than long, rarely isodiametric, 1.0–2.7 μm long. Cell content light to dark green, blue green, brown, and grey. Apical cell rounded, with occasional clear calyptra. Reproduction by fragmentation or hormogonia.','Berthold et al. 2022',NULL,0,0),(2235,2419,'etymology','Latin floridanum, in reference to the widespread occurrence of this cyanobacterium throughout the southern Florida coast.','Berthold et al. 2022',NULL,0,0),(2236,2420,'description','Thallus solitary, floccose, free-floating, light to dark blue green. Filaments straight, wavy to flexuous, without sheath. Trichomes cylindrical, 5.3–6.2 μm wide. Cells slightly constricted between meristematic zones, highly constricted between dividing cells in older filaments. Cross-walls densely granulated and darkened. Cells discoid, wider than long, rarely isodiametric, 1.5–2.9 μm long. Cell content light to dark green, blue green, brown and grey. Apical cell rounded. Reproduction by filament disintegration or fragmentation.','Berthold et al. 2022',NULL,0,0),(2237,2420,'etymology','The epithet guerandense, is a reference to the salt flats in Guérande where the species originates.','Berthold et al. 2022',NULL,0,0),(2238,2421,'description','Thallus amorphous and entangled, mat-like. Filaments straight, 14–18.9 μm in diameter, rarely coiled. Sheath thick, facultative, hyaline, not lamellate. Cells slightly constricted. Cross walls densely granulated. Cells discoid, wider than long, 10.7–14 μm wide, 1.4– 2.4 μm long. Cell content green, green-yellow, and yellow at apices. Apices conical to rounded, without calyptra. Hormogonia formed by straight fragmentation, with or without necridic cells. Diagonal fragmentation occurs with or without necridic cells.','Berthold et al. 2022',NULL,0,0),(2239,2421,'etymology','Latin adjective flavus, -a, -um, yellow, and Latin ending -ceps (caput), head, in reference to the tendency for yellowing of the apices of the trichome.','Berthold et al. 2022',NULL,0,0),(2240,2422,'description','Thallus light to dark forest green, and yellow to orange when exposed to air (drying). Filaments straight to flexuous, 18.5–29.2 μm in diameter, rarely coiled. Sheath thin, facultative, hyaline, not lamellate. Cells not constricted. Cells discoid, wider than long, 15.8–24.9 μm wide, 1–2.2 μm long. Cell content green. Apices conical to rounded, attenuating, without calyptra. Apical cell yellow. Hormogonia formed by straight fragmentation, with or without necridic cells. Diagonal fragmentation occurs with or without necridic cells.','Berthold et al. 2022',NULL,0,0),(2241,2422,'etymology','The epithet guerandensis is a reference to the salt flats in Guérande where the species originates.','Berthold et al. 2022',NULL,0,0),(2242,2424,'description','Thallus tomentose, expanded, and blue-green to yellowish-brown. Filament straight or slightly curved and up to 30 μm in width, a filament contains a solitary trichome, but occasionally two. Sheaths firm and thick, longitudinally and transversely annular lamellated, yellowish-brown in nature. Sheaths initially colorless and later yellow-brown or pink in the culture. Trichome blue to green, constricted at the cross-walls, not attenuated at the end, motile. Cells flat rectangle with L/W 1/3–1/4, 4.2–6.1 μm long and 11.1–23.2 μm wide. Apical cells conical or round without calyptra. Reproduction with hormogonia formed by necridic cells.','Kim et al. 2022',NULL,0,0),(2243,2424,'diagnosis','<em>Porphyrosiphon annulatus</em> had a relatively large trichome by the interspecies comparison, possessed shorter and flatter rectangular cells compared to the type species P. notarisii, and displayed transversely annular lamellations in the sheath.','Kim et al. 2022',NULL,0,0),(2244,2424,'etymology','“annulatus” was named so because sheath yielded a feature of transversely annular lamellations','Kim et al. 2022',NULL,0,0),(2245,2425,'description','Thallus forming olive-green to moss-green mats in culture. Sheath absent. Trichomes straight to slightly waved, unbranched, isopolar, slightly constricted at the cross-walls, not attenuated towards ends, 0.8–1.0 μm diam. Cells 1.6–4.3 μm long, 2.5 times longer than wide. Gas vesicles absent. Apical cells flattened, without calyptra. Necridic cells absent.','De Araújo et al. 2022',NULL,0,0),(2246,2425,'etymology','Specific epithet “epiphyticum” reflects the occurrence of this species growing on a red macroalgae.','De Araújo et al. 2022',NULL,0,0),(2247,2426,'description','Thallus radially spreading, felt with fleecy surface or firm, leathery, dirty grey-blue-green to dark brown. Filaments long, flexuousus and curved, 2.6–4.1 (5.0) μm wide. False branching rare, single and geminate. Sheath thin and colorless or dull grey, with increasing age becoming thick, ocassionally swollen, slightly to intensely brownish, sometimes with sharply outlined almost blackish outer layer. Trichomes slightly constricted and sometimes granulated at cross-walls, 2.2–2.6 μm wide. Cells cylindrical, isodiametric to elongated, with 4-6 parietal thylakoids, 2.2–4.3 μm long. End cells rounded. Necridia present. Trichome fragmentation occurred with or without necridia and led to the formation of short hormogonia.The cell division symmetrical and perpendicular to the long axis of the filament; however in meristematic zones it may be oblique. D1-D1’ helix 67 nucleotides long, with four internal loops at positions 6/54–62, 13-15/45-47, 21/ 39 and 24/35-36, with terminal loop having sequence 5’- CAUG -3’. Box B helix 35 nucleotides long, with two unpaired cytosine residues at positions10 and 30. Terminal loop 5 nucleotides long, 5’-GACAG-3’.V2 helix 10 nucleotides long, terminal loop 4 nucleotides, 5’-AUGA-3’. V3 helix 60 nucleotides long, with two asymmetrical internal loops at positions 5/54-56 and 23/33-34, and two unpaired uracil and adenine residues at positions 46 and 51 of the 3’ strand. Terminal loop 3 nucleotides long, 5’-GAU-3’.','Mikhailyuk et al. 2022',NULL,0,0),(2248,2426,'diagnosis','Differing from all Timaviella species in sheath appearance, length of D1-D1’ and Box-B helices, structure and sequence of the regions above the basal stem.','Mikhailyuk et al. 2022',NULL,0,0),(2249,2427,'etymology','Named for its occurrence in biocrusts on dunes; dunensis (L) = of dunes.','Mikhailyuk et al. 2022',NULL,0,0),(2250,2427,'description','Thallus radially spreading, expanded, leathery, brownish, dark olive, blue-green to light greenish. Filaments long, variously curved, (3.0) 3.8-4.9 (6.0) μm wide. False branching rare, mostly double. Sheath colourless, firm, thick. Trichomes slightly constricted at cross-walls, occasionally becoming almost biseriate due to oblique division and compression of cells, 2.2–3.3 μm wide. Cells cylindrical, isodiametric to longer than wide, with parietal thylakoids, 2.2–3.5 μm long. End cells rounded to conical. Necridia in both young and senescing trichomes, hormogonia rare. D1-D1’ helix 85 nucleotides long, with a 3’ unilateral bulge at position –/ 73-80, five internal loops at position 10/68, 14-15/63-64, 20/58, 23/54-55 and 31/46. Terminal loop having sequence 5’-UCUC-3’. Box B helix 48 nucleotides long, with several assymetrical internal loops at position 6/41–42, 9–10/39 and –/30–32. Terminal loop 5 nucleotides long, 5’-AUAAU-3’. V2 helix 10 nucleotides long, terminal loop 4 nucleotides, 5’-AUUA-3’. V3 helix 60 nucleotides long, with several internal loops at positions 4/53–55, 9–10/47–50 and 23/34. Terminal loop having sequence 5’-GAAA-3’.','Mikhailyuk et al. 2022',NULL,0,0),(2251,2427,'diagnosis','Morphologically and ecologically similar to T. edaphica differing in the colorless sheath, wider filaments and trichomes, conical end cells, longer Box-B and D1-D1’ helices; structure of V3 helix in the position 9-50 and of basal stem and terminal loop in V2. Differs from T. circinata in Box-B and V3 helices length, the structure in the D1-D1’, Box-B and V3 helices, as well as the color of thallus, rare false branching, wider trichomes, parallel thylakoids and presence of necridia.','Mikhailyuk et al. 2022',NULL,0,0),(2252,2428,'description','In environmental material, thallus is caespitose up to 0.5 cm high, formed by blue-green to dark green entangled, abruptly attenuated filaments (Fig. 6, K–M), sometimes with a small apical bead-like protuberance, not forming a hair, with hemicircular basal heterocytes and subquadrate to longer intercalary heterocytes (10–12 9 12–20 um wide/long), sheaths hyaline to yellow-brown, lamellated (Fig. 6, L–N). Filaments are iso- and heteropolar, slightly curved, with double and single false branching, 20–30 um wide. Trichomes are not to slightly constricted, 9–15 lm wide. Cells are shorter than wide, 3–6 um long. Heterocytes are shorter than wide. Reproduction is by hormogonia 40–60 um long, mainly isopolar, formed by trichome fragmentation or by biconcave lens-shaped necridia, generally developing into heteropolar young filaments (Fig. 6, F–G, J). Akinetes are not observed. In culture, filaments are heteropolar with lamellated, hyaline sheaths (Fig. 6A). Trichomes constricted at cross walls, thickened at the base, gradually attenuated, and ending in a hair (Fig. 6, C and D). Cells are granulated, shorter than wide (Fig. 6, A and B), 3–7 lm long. Necridia is uncommon, light bluegreen. Heterocytes are basal and intercalary, scarce, hemispherical, spherical to oval-cylindrical, solitary, 7–10 um wide. Reproduction is by iso- and heteropolar hormogonia that develop from one or more cells and remain for some time in chains within the sheath (Figs. 6, F–J). Akinetes are not observed.','Johansen et al. 2021',NULL,0,0),(2253,2428,'etymology','<em>komarkovae </em>(L.) = dedicated to Jarka Komarkova, a renowned cyanobacterial researcher and friend, who we miss keenly.','Johansen et al. 2021',NULL,0,0),(2254,2429,'description','In environmental material, thallus is caespitose up to 1–2 mm high, formed by bluegreen to dark green apically attenuated filaments, densely entangled at the base with basal and intercalary heterocytes (Fig. 7, B and C). Sheaths are open hyaline to yellow-brown, lamellated (Fig. 7, A–E). Filaments are iso- and heteropolar, slightly curved, with double and single false branching (see Gonzalez-Resendiz et al. 2015, fig. 4, A for C701), 10–30 um wide, wider at basal parts. Trichomes are not slightly constricted, 8–16 um wide. When mature, isopolar filaments sometimes erect at both attenuated ends and frequently forming hair (Fig. 7A). Cells are shorter than wide, 4–9 um long. Apical cells are slightly attenuated, sometimes forming a short, nonhyaline hair. Heterocytes are scarce, generally shorter than wide, mostly 3–6 um long (Fig. 7B). Reproduction is by terminal or basal hormogonia 30–70 (80) um long, iso- or heteropolar, formed mainly by biconcave lens-shaped necridia or trichome fragmentation, generally developing into heteropolar young filaments (Fig. 7C). Akinetes are not observed. In culture, filaments are heteropolar with lamellated, hyaline, apically open sheaths (Fig. 7, E–F, H, K). Trichomes constricted at cross-walls, thickened at the base, gradually attenuated, and ending in a hair (Fig. 7, E–G). Cells are granulated, shorter than wide in main portion and also in the tapered region of trichomes (Fig. 7K). Necridia are dark blue-green, biconcave lens-shaped. Heterocytes are scarce, basal and intercalary, hemispherical, spherical to oval-cylindrical, complanate, solitary, and sometimes two together 12–14 um long. Reproduction is by basal hormogonia; consisting of flattened or irregularly twisted or contorted cells enclosed in a widened sheath (Fig. 7, H–J). Basal hormogonia sometimes separate from the filament, and later, every cell has the ability to develop into small iso- orheteropolar hormogonia that are released (Fig. 7, E, H–J).','Johansen et al. 2021',NULL,0,0),(2255,2429,'etymology','<em>sanagustinensis </em>(L.) = from San Agustın, Oaxaca in Pacific Mexico','Johansen et al. 2021',NULL,0,0),(2256,2430,'description','In environmental material, thalli crustaceous is flat, up to 1 cm in diameter, formed by colonies of bluegreen to dark green loosely parallelly disposed erect, straight or flexuous filaments, 125–230 um high (Fig. 8, A and B). Sheaths are gelatinized but lamellated, hyaline at the base and central parts, becoming slightly yellow-brown or golden at the upper apices of the filaments (Fig. 8, B, D–I), sometimes becoming widened and diffluent at apical parts. Filaments are apically attenuated, isopolar, folded at the base, commonly forming simple loops, occasionally forming lateral foldings giving a branched appearance (Fig. 8, A, C, E, G, J). Single, individual filaments 9–17 (20) um wide and (11) 18–22 um wide when folded double (Fig. 8, B, D–H). Trichomes are slightly to very constricted at cross-walls, 4.6–6 um wide. Cells are variably shaped, from subquadrate to trapezoidal or barrelshaped, 2.6–6.1 um long (Fig. 8, D–H). Heterocytes are intercalary, solitary, variably shaped from subspherical, short cylinders to quadrate (4.3) 5–11.1 (14.6) um long (4.6) 6–10.1 um wide (Fig. 8, D, F, H, K,). Reproduction is by terminal iso- or heteropolar, generally thin hormogonia, 4–7 um wide (12.2) 19–30 um long (Fig. 8, G and I). Akinetes are not observed.','Johansen et al. 2021',NULL,0,0),(2257,2430,'etymology','(L.) = from Playa Munecos (Doll’s Beach), Veracruz in the Gulf of Mexico','Johansen et al. 2021',NULL,0,0),(2258,2431,'description','In environmental material, thalli are crustaceous flat, up to 1 cm in diameter, formed by colonies of blue-green to dark green parallelly disposed filaments with intercalary heterocytes, 80–230 um high (Fig. 9, A and B), with sheaths firm, lamellated, hyaline at the base and central parts (Fig. 9, A–D), can become yellow-brown or golden at the upper apices. Filaments are isopolar folded at the base, forming generally simple loops and occasionally forming lateral foldings giving a branching appearance (Fig. 9C), apically attenuated. Single, individual filaments 8–10 um wide and double (folded) 13–24 um wide. Trichomes are slightly (rarely) to commonly very constricted but with long series of similar width cells 5–8 um wide (Fig. 9, A–D, G). Cells are variable from subquadrate to trapezoidal or barrel shaped, with cells 4–8.5 um long, apical hair cells 5–7 um long, 2.8–4.5 um wide. Heterocytes are solitary, intercalar or terminal in some hormogonia, variable from subspherical, short cylinders to quadrate (4) 5–6 (10) um long, (5) 7–9 (12) um wide (Fig. 9, E and F). Fragmentation is by terminal iso- or heteropolar, generally thin, hormogonia, 3–5 um wide, 25–51 um long (Fig. 9, D and E). Akinetes are not observed. In culture material, filaments lose their parallel arrangement, becoming contorted and entangled, generally very sinuous or irregularly folded, with only a few showing a parallel disposition, individually 11–19 um wide, when doubled 24–42 um wide. Sheaths are hyaline, gelatinized, lamellated. Trichomes are very constricted at the cross walls, 6–9.5 um wide. Cells are blue-green, variably shaped, 4–7.7 um long. Heterocytes are intercalary, uncommon, variably shaped 7–8 um wide. Hormogonia<br>without sheath, with 2–3 semicircular cells, 10–12 um long. Akinetes are not observed.','Johansen et al. 2021',NULL,0,0),(2259,2431,'etymology','(L.) = from prehispanic Totonaca region, Veracruz in the Gulf of Mexico','Johansen et al. 2021',NULL,0,0),(2260,2432,'description','Thallus dark blue-green. Filaments entangled, 7.0–11.0 μm wide. Sheaths firm, thin, homogeneous, colorless. Trichomes cylindrical, not attenuated, constricted at the ungranulated cross walls, 5.5–8.0 μm wide. Cells cylindrical, isodiametric, shorter or longer than wide, 3.0–7.5 μm long. Cell content blue-green, granulated. Apical cells slightly conical-rounded, with thickened cell wall, sometimes with yellow cell content, 6.0 μm long.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2261,2432,'etymology','L. adj. <em>caatingensis </em>= from Brazilian biome Caatinga','Machado de Lima &amp; Branco 2020',NULL,0,0),(2262,2433,'description','Thallus dark blue-green. Filaments with many trichomes per sheath, 8.0–32.0 μm wide. Sheaths firm, thin, homogeneous, colorless. Trichomes cylindrical, not attenuated, constricted at the ungranulated cross walls, 4.8–6.40 μm wide. Cells cylindrical, isodiametric, shorter or longer than wide, 3.2–8.8 μm long. Cell content blue-green, granulated. Apical cells slightly conical-rounded, with thickened cell wall, sometimes with yellow cell content, 8.0–8.8 μm long.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2263,2433,'etymology','G. n. <em>edaphos </em>= soil, ground; <em>edaphica </em>= from soils','Machado de Lima &amp; Branco 2020',NULL,0,0),(2264,2434,'description','Filaments entangled among soil granules. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, unconstricted at the cross walls. Cells cylindrical, isodiametric to longer than wide. Cell content finely granular. Apical cell conical-rounded to conical-obtuse, without calyptra. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2265,2434,'etymology','L. adj. <em>gracilis </em>simple, modest; L. noun fem. <em>linea </em>line/filament; Gr<em>​</em>acilinea = simple filament','Machado de Lima &amp; Branco 2020',NULL,0,0),(2266,2435,'description','Filaments entangled among soil granules, 4.0–7.0 μm wide. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, unconstricted at the cross walls, 4.0–5.0 μm wide. Cells cylindrical, isodiametric to longer than wide, 4.0–10.0 μm long. Cell content finely granular. Apical cell conical-rounded to conical-obtuse, without<br>calyptra, 7.5–10.0 μm long. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2267,2435,'etymology','L. n. <em>arena </em>= sand; L. suffix <em>cola </em>= inhabitant; <em>arenicola </em>= inhabiting sandy substrates','Machado de Lima &amp; Branco 2020',NULL,0,0),(2268,2436,'description','Filaments entangled among soil granules. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, constricted at the cross walls. Cells cylindrical, shorter than wide. Cell content blue-green to dark green, keratomized. Apical cell conical-rounded, without calyptra. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2269,2436,'etymology','G. noun. <em>marmor </em>= marble; L. noun. <em>cella </em>= room, cell, <em>Marmoreocelis</em>-referring to the cell with marble aspect due to keritomy','Machado de Lima &amp; Branco 2020',NULL,0,0),(2270,2437,'description','Filaments entangled among soil granules, 6.8–8.0 μm wide. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, constricted at the cross walls, 6.0–7.2 μm wide. Cells cylindrical, shorter than wide, 2.4–6.2 μm long. Cell content blue-green to dark green, keratomized. Apical cell conical-rounded, without calyptra, 5.2–11.2 μm long. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2271,2437,'etymology','G. adj. <em>xeros </em>= dry; G. noun. <em>phílos </em>= friend; <em>xerophila </em>= occurring in dry, xeric habitat','Machado de Lima &amp; Branco 2020',NULL,0,0),(2272,2438,'description','Filaments entangled among soil granules. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, constricted at the cross walls. Cells cylindrical, shorter than wide. Cell content blue-green, granulated. Apical cell conical to pointed, without calyptra. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2273,2438,'etymology','G. adj. <em>konikó</em> = conical; Gr. n. <em>akro</em> = tip; Gr. <em>nema </em>= filament; <em>Konicacronema </em>= filament with conical apical cell','Machado de Lima &amp; Branco 2020',NULL,0,0),(2274,2439,'description','Filaments entangled among soil granules, 4.0–7.0 μm wide. Sheaths firm, thin, colorless, hyaline. Trichomes isopolar, not attenuated at the ends, constricted at the cross walls, 4.0–6.0 μm wide. Cells cylindrical, shorter than wide to isodiametric, 2.4–5.0 μm long. Cell content blue-green with brown/yellow granules. Apical cell conical to pointed, without calyptra, 4.0–9.0 μm long. Reproduction via hormogonia.','Machado de Lima &amp; Branco 2020',NULL,0,0),(2275,2439,'etymology','L. adj. <em>caatingensis </em>= from Brazilian biome Caatinga','Machado de Lima &amp; Branco 2020',NULL,0,0),(2276,44,'description','<em>Emended Description</em>: Desiccation-resistant, filamentous cyanobacteria, mostly terrestrial, but also found in intertidal zones. Filaments are solitary or entangled and forming mats. Filaments are without branching, heterocysts, necridia, or akinetes. Trichomes are cylindrical, uniseriate, iso- or heteropolar, slightly or very constricted to not constricted, and with thin colorless to thick colored sheaths; trichomes enveloped by a common sheath are frequently found in the family. Apical cells are attenuated, elongated and conical or elongated and pointed, or rounded with no calyptra. Trichomes and cultures are blue green in color. Cells  isodiametrical or slightly shorter or longer than wide, with fasciculated to radial, sometimes irregular thylakoids arrangement. Cell content is homogeneous to finely granulated, sometimes with scattered larger granules. Reproduction by disintegration of trichomes into hormogonia is present in the family. Sunscreens pigments such as mycosporine-like amino acids (MAAs) are present in at least two genera of the family as are light harvesting pigments such as phycoerythrocyanin. Gliding motility is very often present.','Fernandes et al. 2021',NULL,0,0),(2277,2440,'description','Terrestrial, common in cool desert soils. Trichomes are cylindrical, 5–7 μm wide, iso- or heteropolar, constricted at the cross-walls, sometimes attenuated toward the apex, with facultative, thin to thick, colorless, hyaline sheaths that can be open at the end and extend outside the filament; multiple trichomes enveloped by a single sheath are common. Apical cells are conical and elongated or rounded. Cells are elongated to quadratic and granulated.','Fernandes et al. 2021',NULL,0,0),(2278,2440,'etymology','Allocoleopsis Allo.cole.o’psis. Gr. adj. allos, other; N.L. n. coleus from Greek koleon, sheath; Gr. suffix –opsis, looking like. Allocoleopsis, looking like another coleus.','Fernandes et al. 2021',NULL,0,0),(2279,2441,'description','Solitary filaments or bundled into rope like structures. Trichomes are heteropolar, 5–6 μm wide, slightly constricted at cross-walls (visible under light microscopy at 1009), with thin or diffluent and colorless sheaths that do not open at the end. Trichomes are olive green in culture. Cells are elongated to quadratic, 6–7.5 μm long and 5–6 μm wide. Apical cells are rounded to slightly conical. Mesophilic grows between 10°C and 35°C and it is sensitive to temperatures below 10°C. Growth is optimal at 35°C. Commonly found in biological soil crusts but uncommon in hot deserts.','Fernandes et al. 2021',NULL,0,0),(2280,2441,'etymology','Allocoleopsis franciscana fran.cis.ca.na L.- suffix -an native of, relating to. Franciscana, referring to the isolation area, San Francisco, California.','Fernandes et al. 2021',NULL,0,0),(2281,2442,'description','Terrestrial. Filaments are solitary or entangled. Trichomes are cylindrical, around or slightly less than 4 μm wide, very constricted, with thin, colorless sheaths that open at the end and extend outside the filament. Multiple trichomes enveloped by a single sheath are common. Apical cells are pointed, longer than wide. Taper involves apical cell only. Cells are quadratic and granulated.','Fernandes et al. 2021',NULL,0,0),(2282,2442,'etymology','<em>Funiculus </em>Fu.ni’.cu.lus. L. m. n., <em>funiculus</em>, a small or slender rope.','Fernandes et al. 2021',NULL,0,0),(2283,2444,'description','Solitary filaments or bundled into rope like structures. Trichomes are heteropolar, highly constricted at cross-walls (visible under light microscopy at 400x and 1,000x), with thin or diffluent and colorless sheaths that open at the end and extend outside the filament. Cells are quadratic to shorter than wide, 2.5–4 μm long, and finely<br>granulated. Apical cells are pointed and elongated. Mesophilic grows between 4 and 35°C, and it is sensitive to temperatures below 4°C. Growth is optimal at 30°C.','Fernandes et al. 2021',NULL,0,0),(2284,2444,'etymology','Funiculus tenuis te’.nu.is L. adj. tenuis, delicate.','Fernandes et al. 2021',NULL,0,0),(2285,2445,'description','Terrestrial. Solitary filaments or bundled into rope like structures. Trichomes are slightly constricted (visible under light microscopy at 1,000x), cylindrical, iso- or heteropolar, 7 - 8.5 μm wide. Sheaths facultative, thin, colorless, hyaline, and sometimes open at the end and extend outside the filament. Apical cells are rounded, sometimes elongated. Cells are quadratic to shorter.','Fernandes et al. 2021',NULL,0,0),(2286,2445,'etymology','Cra.ssi.fi’.lum. L. crassus, thick or stout. Crassifilum, thick filament.','Fernandes et al. 2021',NULL,0,0),(2287,2446,'description','Filaments are solitary or entangled. Trichomes are slightly constricted at cross-walls (visible under light microscopy at 1,0009), with thin, colorless sheaths, sometimes sheaths open at the end and extend outside the filament. Mostly one trichome per sheath, sometimes two. Cells are quadratic to shorter than wide, 6–7.5 μm long and 7.5–8.5 μm wide. Apical cells are rounded, not tapered, sometimes elongated. Mesophilic grows at 10–40°C, and it is sensitive to temperatures below 10°C. Growth is optimal at 35°C.','Fernandes et al. 2021',NULL,0,0),(2288,2446,'etymology','Crassifilum sonorensis so.no.re’n.sis (L. demonym, originating from Sonoran Desert).','Fernandes et al. 2021',NULL,0,0),(2289,2447,'description','Terrestrial. Filaments solitary or entangled. Trichomes are thin, cylindrical, around or slightly less than 4 μm wide, constricted to not constricted at cross-walls. Sheaths facultative, thin to thick, colorless, hyaline, sometimes open at the end and extend outside the filament. Multiple trichomes enveloped by a single sheath are common, sometimes twist simulating a knot or a spiral. Apical cells are conical, but sometimes pointed, no calyptra. Cells are quadratic or slightly shorter or longer than wide, and finely granulated.','Fernandes et al. 2021',NULL,0,0),(2290,2447,'etymology','Arizonema A.ri.zo.ne’ma. NL. Arizona a U.S. State, prob. from Tohono O’Odham alı ṣonak, little spring; Gr.n.n. nema filament. Arizonema, Arizonan filament.','Fernandes et al. 2021',NULL,0,0),(2291,2448,'description','Filaments are solitary or form bundles. Trichomes are not constricted at cross-walls. Filaments with thin or diffluent and colorless sheaths sometimes open at the end and extend outside the filament. Cells are quadratic to shorter than wide, 2.8–3.8 μm long. Apical cells are pointed or conical, sometimes with bulge on either side, sometimes tapered. Mesophilic grows at 10–35°C and is sensitive to temperatures below 10°C. Growth is optimal at 30°C.','Fernandes et al. 2021',NULL,0,0),(2292,2448,'etymology','<em>Arizonema commune</em> com.mu’.ne L.n.a. <em>commune </em>common, universal.','Fernandes et al. 2021',NULL,0,0),(2293,2449,'description','Terrestrial. Filaments are solitary or tangled. Trichomes are cylindrical, around or slightly less than 5 μm wide, are slightly constricted at cross-walls with facultative, thin, colorless, hyaline sheaths. Multiple trichomes enveloped by a single sheath are common. Apical cells are rounded, but sometimes can be conical. Cells are quadratic or longer than wide, granulated, and cell wall is welldefined.','Fernandes et al. 2021',NULL,0,0),(2294,2449,'etymology','<em>Crustifilum </em>Crus.ti.fi’.lum. L.f.n. <em>crusta </em>crust. L.n.n. <em>filum</em>, thread. <em>Crustifilum </em>thread of crust.','Fernandes et al. 2021',NULL,0,0),(2295,2450,'description','Filaments are solitary or form bundles. Trichomes are slightly constricted at cross-walls (visible under light microscopy at 1,000x). Apical cells are elongated and conical or elongated and rounded, sometimes paler that the rest of the trichome. Cells are quadratic or longer than wider, 5–7 μm long, granulated with well-defined cell walls. Mesophilic grows at 4–35°C, and it is sensitive to temperatures below 4°C. Growth is optimal at 25°C.','Fernandes et al. 2021',NULL,0,0),(2296,2450,'etymology','<em>Crustifilum hispaliculae</em> his.pa.li.cu.lae. L. n. Hispalis, the city of Seville; L. diminutive suffix, -<em>cula</em>; N.L. f.n., <em>hispaliculae</em>, of the small Seville, from the location of Sevilleta, New Mexico.','Fernandes et al. 2021',NULL,0,0),(2297,2451,'description','Terrestrial. Filaments are solitary or bundled into rope like structures. Trichomes are cylindrical, around or slightly less than 5 μm wide, slightly constricted at cross-walls. Sheaths facultative, thin, colorless, hyaline. Multiple trichomes enveloped by a single sheath are common, sometimes twist simulating a knot or a spiral. Apical cells are always rounded. Cells are quadratic to longer than wider.','Fernandes et al. 2021',NULL,0,0),(2298,2451,'etymology','<em>Parifilum </em>Pa.ri.fi.lum. L. n. n. <em>par </em>doublet, set of two; L. n. n<em>&nbsp;filum</em>, thread. <em>Parifilum</em>, thread made of doublets.','Fernandes et al. 2021',NULL,0,0),(2299,2452,'description','Filaments are solitary or entangled. Trichomes are slightly constricted at cross-walls (visible under light microscopy at 1,000x) and more constricted every two cells with facultative, thin or diffluent and colorless sheaths that do not open at the end. Cells are quadratic to elongated, 5–7 μm long. Apical cells are always rounded. Mesophilic grows at 10–35°C, and it is sensitive to temperatures below 10°C. Growth is optimal at 15°C.','Fernandes et al. 2021',NULL,0,0),(2300,2452,'etymology','<em>Parifilum solicrustae</em> L. n. n. <em>solum</em>, soil.; L. f. n. <em>crusta</em>, crust; N. L, <em>solicrustae</em>, of the soil crust.','Fernandes et al. 2021',NULL,0,0),(2301,2453,'description','Observed under the light microscopy the filaments of A121 strain were blue-green, thin, straight, bent, wavy, and occasionally curved (Figure 5). Trichomes observed with TEM show barrel shaped cells forming a single filament without any branching; meanwhile, SEM and light microscopy photos indicate much longer filaments. Trichomes observed in longitudinal direction were characterized by long cylindrical cells with contraction in the transverse wall. Typical length of each cell ranged from 2.0 to 3.0 um and had a width of 0.9–1.4 um (Figure 5). Each of the cylindrical cells was separated from a neighboring cell with centripetal invagination of the cell wall, and no connections between the cells were observed. Each of the cells had between three and five thylakoid layers located in parallel on the inner periphery of the cells. Cells were observed to contain carboxysomes, cyanophycin granules, and polyphosphate bodies. The strain was motile. The strain was capable of growing in standard BG11 medium at a maximal temperature of 50°C and in the presence of 0.1 M NaHCO3. The strain can be successfully cryopreserved in 10% DMSO for a period exceeding 24 months.','Tang et al. 2022',NULL,0,0),(2302,2453,'etymology','Species epithet derives from the name of the collection site.','Tang et al. 2022',NULL,0,0),(2303,2454,'description','Colonies are filamentous, with densely and parallel packed trichomes, enveloped by colourless, delimited distinct slime, blue–green, forming rough mats in strong development. Trichomes very rarely ± solitary (initial stages), usually in fascicles, straight, waved to slightly curved, with the same width along the whole length, unbranched, constricted at cross–walls, with very indistinct own sheaths, or without them. Cells barrel–shaped to cylindrical, blue–green, ± isodiametric to slightly longer than wide, 1.5˗2 × ± 1.6 μm wide, apical cells rounded–pointed. Heterocytes intercalary, oval to barrel–shaped, very slightly wider than vegetative cells. Young akinetes cylindrical, later oval, elongate, larger than the vegetative cells, situated to both sides of a heterocyte, solitary, rarely a few in short rows, smooth at the surface, with a slightly brown exospore, 7–10 × 3.2–4.5 μm.','Kozlíková-Zapomělová et al. 2016',NULL,0,0),(2304,2454,'etymology','specific name according to the character of habitat','Kozlíková-Zapomělová et al. 2016',NULL,0,0),(2305,678,'description','Colonies spreading, green to blue–green, mucilaginous, amorphous. Sheaths absent. Trichomes thin, mostly bright blue–green (aquamarine), usually straight or slightly bent, dispersed evenly and loosely without mat formation, unconstricted or only indistinctly constricted at cross–walls. Sheaths absent. Trichomes cylindrical, straight, not capitate, motile with intense gliding in the direction of the longitudinal axis, sometimes accompanied by bending and distinctive rotation, 1–3 μm wide. Cells usually 2–4 longer than wide, 4–8 μm long, sometimes with visible peripheral chromatoplasma, sometimes with evident carotenoid granules, without aerotopes, after division growing to the size of the mother cells before the next cell division. Apical cells in developed trichomes bent, narrowed and pointed–rounded, never calyptrate or capitate. Thylakoids parietal, with triangle or rhombic organization in transversal section. Reproduction by disintegration of trichomes in hormogonia without necridic cells.','Strunecký et al. 2017',NULL,0,0),(2306,678,'etymology','Named in memory of the prominent late cyanobacterial specialist Konstantinos Anagnostidis, combined with the Greek word nema – a cable.','Strunecký et al. 2017',NULL,0,0),(2307,2467,'description','Microscopic; spherical to hemispherical cells, solitary or forming colonies; reproduction by binary fission; thylakoids arranged parietally; individual mucilaginous envelopes facultative, rarely present.','Soares et al. 2022',NULL,0,0),(2308,2468,'description','Microscopic; when in nature, growing on limestone surfaces. In liquid media, growing on the bottom of test tubes, sometimes forming thin biofilms attached to test tube walls. Color of cultures green, olivaceous-green, or yellow; cells spherical to hemispherical, solitary or forming colonies with a variable number of cells in compacted aggregates; reproduction by binary fission; thylakoids arranged parietally; with facultative, rarely present, individual mucilaginous envelopes.','Soares et al. 2022',NULL,0,0),(2309,2468,'etymology','The genus name was derived from the Greek words pέsqa, Petra, meaning stone/rock, and vkxqός, chloros/khlοros, meaning green.','Soares et al. 2022',NULL,0,0),(2310,2469,'description','Microscopic, growing on limestone surfaces. Color of cultures green, olivaceous-green, or yellow. Cells spherical to hemispherical, solitary or forming colonies with a variable number of cells in compacted aggregates; young cells rounded, 0.5–1.7 μm in diameter; mature cells enlarged, 1.3–1.9 μm; elongated cells before division, 1.3–3 μm in diameter; reproduction by binary fission in one plane parallel to the short axis; thylakoids arranged parietally; facultative, rarely present, mucilaginous envelopes.','Soares et al. 2022',NULL,0,0),(2311,2469,'etymology','The species name refers to the royal charter “Scientiae thesaurus mirabilis” signed by King D. Dinis in 1290 when the University of Coimbra, the first University in Portugal, was created.','Soares et al. 2022',NULL,0,0),(2312,2470,'description','Thallus flat, thin mat, blue-green, filaments flexuous, rarely with more than one trichome in common mucilage, with sheath 1.0–1.5 μm wide. Sheath hyaline, non-lamellate, colorless, in older filament rarely widened with wavy edges. Trichomes motile constricted at the crosswalls, without granulation at the crosswalls or in cytoplasma, parietal position of thylakoid clearly visible in electron microscopy micrographs (Fig. 1c–h). False branching lacking, necridic cells not produced. Cells consistently longer than wide, 0.9–1.1 (1.2) μm wide and (1.2) 1.5–1.8 (2.2) μm long. Apical cells rounded or rounded conical, generally longer than vegetative cells (1.9–5.6 μm) (Fig. 1d–f), with a reddishorange spot in the apex (Fig. 1d). Contains phycocyanin (PC) but not phycoerythrin (PE)(Fig. S1).','Brito et al. 2022',NULL,0,0),(2313,2470,'etymology','Lusitanica—from Portugal','Brito et al. 2022',NULL,0,0),(2314,2470,'diagnosis','<em>Oculatella lusitanica</em> does not have distinct morphological characteristics, sharing morphological features with the different <em>Oculatella </em>species. It is blue-green as the majority of the species described, differing in color from the type species, <em>Oculatella subterranea</em> Zammit, Billi &amp; Albertano, which is reddish. While <em>O. subterranea </em>contains PC and PE, <em>O. lusitanica</em> contains only PC. The width of <em>O. lusitanica</em> filaments (1.0–1.5 μm) is similar to that reported for <em>O. crustae-formantes</em> (0.8–1.6 μm), the species with the thinner filaments described within the genus, and to<em> O. cataractarum</em> (1.3–1.7 μm) and <em>O. kauaiensis</em> (1.2–1.7 μm). The trichome width is also in the same range of the three mentioned species. Similarly to <em>O. crustae-formantes</em> (1.2–2.9 μm), <em>O. lusitanica</em> has shorter cell length (1.5–3.0 μm) compared to other species. In addition, it does not have granules at crosswalls as reported for some strains (<em>O. subterranea, O. kauaiensis, O. coburnii, O. leona</em> and <em>O. dilatativagina</em>). A morphological comparison between <em>O. lusitanica</em> and all known <em>Oculatella </em>species is depicted in Table 1, and the determination key for <em>Oculatella </em>genus leading to the identification of <em>Oculatella lusitanica</em> is shown in Fig. S2.','Brito et al. 2022',NULL,0,0),(2315,2471,'description','The thallus is blue-green, macroscopic, in aggregates. Filaments are straight or bent, unbranched, solitary, and free-floating. The sheath is soft, layered, colorless, adherent to the edges of the cells, often becoming wide. Trichomes are isodiametric, constricted at the cross walls, and forming long, loose spirals under normal light condition; nodules are present under low light intensity (&lt;4 umol/(m-2.s-1)). Cells are green to blue-green, lacking a gas vesicle, slightly cylindrical, more or less longer than they are wide, 1.02–1.75–2.74 um long, and 1.10–1.10–1.34 um wide, with a length: width ratio of 1.0–2.42; the cell content is divided into peripheral chromatoplasma and central nucleoplasma. The thylakoids are parietally arranged (four or five per cell) (Figure 3). Reproduction is by hormogonia or trichome breakage.','Cai et al. 2022',NULL,0,0),(2316,2471,'etymology','hunanesis refers to the Hunan province where the strain was isolated, transliterated into Latin','Cai et al. 2022',NULL,0,0),(2317,2472,'description','Growing as a soft macroscopic mat on wet soils, with visible blue green color. Filaments loosely or densely entangled, sometimes straight. Sheath colorless, thin, or slightly thick, distinct or gelatinized. Trichomes isopolar, straightly or curved, blue-green, distinctly constricted at the cross-walls, attenuated at the ends. Vegetative cells barrel-shaped to spherical or cylindrical, 3.20-3.41-4.95-μm long, 3.40-3.62-4.78-μm wide. Heterocytes usually intercalary, rarely terminal, spherical or barrelshaped, 3.53-3.84-4.77-μm long, 3.20-3.59-4.15-μm wide. Akinetes intercalary, elliptical, 5.01-5.85-6.72-μm long, 2.24-3.24-3.50-μm wide.','Cai et al. 2022',NULL,0,0),(2318,2472,'etymology','jiangxiense refers to Jiangxi province where the strain was isolated, transliterated into Latin','Cai et al. 2022',NULL,0,0),(2319,2473,'description','Filaments straight, loosely or densely entangled. Sheath colorless, thin, usually invisible. Trichomes isopolar, straightly or curved, blue-green, distinctly constricted at the cross-walls. Vegetative cells spherical to cylindrical, 2.15-3.79-5.21-μm long, 2.05-2.25-4.89-μm wide. Heterocytes usually intercalary, rarely terminal, 3.30-3.59-4.25-μm long, 2.90-3.05-4.40-μm wide. Akinetes intercalary, oval, 5.19-5.72-6.00-μm long, 3.68-3.87-4.18-μm wide.','Cai et al. 2022',NULL,0,0),(2320,2473,'etymology','yunnanense refers to Yunnan province where the strain was isolated, transliterated into Latin','Cai et al. 2022',NULL,0,0),(2321,2474,'description','Blue–green mat–like biofilm; isopolar filament with 3.94–(5.43)–9.45 μm in width, cylindrical, continually widened toward the basal zone, single or binary false branching, sometime single false branching present after loop–like lateral formation, filament densely arranged; sheath thin, smooth, sometime rough, distinct in texture colorless and rarely up to brownish; sheath present throughout the length of trichome; trichome cylindrical, constricted or unconstricted at cross–walls, less or absent constrictions in younger filaments but distinct in older filaments, basal parts widened, terminal parts of branches slightly cylindrical, with rounded–tapering apical ends; vegetative cell cylindrical to disc–like shape with 2.38–(4.49)–12.77 μm in length and 2.85–(4.27)– 0.70 μm in width, with granular content, young cells mostly longer than wide, whereas old cells were shorter than width, blue–green in color; apical cell conically rounded without calyptra and less presence of sheath covering; heterocytes intercalary, cylindrical to discoid shape; single or in pairs; length ranging from 4.20–(7.39)–12.74 μm, whereas the width ranging from 3.84–(5.24)–7.62 μm; reproduction by homogonia; akinetes not present. D1–D1′ helix of the 16S–23S rRNA ITS region with 99 nucleotide long, V2 helix with 67 nucleotides, Box–B with 31 nucleotides, V3 helix with 88 nucleotides with five internal loops; both tRNA coding isoleucine and alanine were present.','Tawong et al. 2022',NULL,0,0),(2322,2474,'etymology','From the Latin “<em>foetidum</em>”; this species produces an earth/musty odor.','Tawong et al. 2022',NULL,0,0),(2323,2475,'description','Thallus flat, in the form of upright tufts with visible filaments on the substrate, blue-green, olive-green, or brown-green. Filaments short to long, single or rarely false branched, heteropolar. Sheath thick, firm, clearly delimited, in old cultures widened, distinctly layered, closed at the ends or becoming diffluent towards the ends, colorless. Trichomes constricted at crosswalls, not tapered or distinctly gradually tapered, slightly or distinctly swollen at the base, 2.9–9.1 m wide. Cells shorter than wide, isodiametric or sometimes longer than wide, barrel-shaped, cylindrical, to almost spherical or spherical compressed, with smooth to finely granulated content, olive-green, brown, purplish-grey, or blue-green, 3.1–10.6 long. End cells conical, conical rounded, or rounded. Heterocytes terminal, with smooth pale-yellow content, shorter than wide, hemispherical or spherical, pale green, 5.0–7.4 m wide, 3.3–5.3 m long. Hormogonia short, with cells 3.5–6.5 m wide, 1.4–6.5 m long. Arthrospores forming in chains, released from one side or the end of filament by destruction of the sheath, 6.7–8.9 m wide, 3–7.1 m long. In old cultures some filaments tightly coiled and variously curved.','Gaysina et al. 2022',NULL,0,0),(2324,2475,'etymology','From the Latin volcanica (=from volcano), referring to the habitat of origin of the taxon.','Gaysina et al. 2022',NULL,0,0),(2325,2476,'description','Filaments with spherical cells with net-like (?keritomic) content, short or long, firstly uniseriate, elongating through binary divisions. Later filaments ramificate with consequently increasing density through specific successive division and visible cell-wall remnants, with branches lying in more than one plane and a subsequent formation of claviform blue-green cells. Claviform cells firstly are with net-like content, but soon become homogenous. They divide mainly longitudinally, in multiple consecutive divisions, forming complex clusters, but remain connected on a common stalk. Each cluster contains numerous typical small groups of four. Single spherical spores restore the filamentous stage by binary transversal divisions. More rarely, it can develop through multiple divisions of a spherical cell released from the top of the claviform cell after its single transversal division. Free-floating in the phytoplankton of a small tropical lake.','Stoyneva-Gärtner et al. 2021',NULL,0,0),(2326,2476,'diagnosis','The present genus differs from <em>Cyanocystis </em>Borzi mainly by the presence of two different stages in the life cycle, by its peculiar division and reproduction as well as by free-floating mode of life in the limnoplankton.','Stoyneva-Gärtner et al. 2021',NULL,0,0),(2327,2476,'etymology','Combination of the Latin name of the genus <em>Cyanocystis </em>and suffix -<em>opsis</em>, which means ‘looking like’.','Stoyneva-Gärtner et al. 2021',NULL,0,0),(2328,2477,'description','Filaments with spherical cells with net-like (?keritomic) content, up to 6 – 6.5 μm in diameter. Filaments are short or long, firstly uniseriate, elongating through binary divisions, with cells reaching 10 –12 μm length during division. Later filaments ramificate intensively through specific successive division and visible cell-wall remnants between the cells, with branches lying in more than one plane and a subsequent formation of claviform blue-green cells, (8) –10 – (12) μm long. Claviform cells firstly are with net-like content, similar to the content of the filamentous stage, but soon become homogenous. They divide mainly longitudinally, in multiple consecutive divisions, thus forming complex clusters (45 – 85 –100 –125 μm in diameter), but remain connected on a common stalk in typical smallest groups of four. Single spherical spores (which almost immediately achieve the net-like content) restore the filamentous stage by binary transversal divisions. More rarely, the filamentous stage can develop directly through multiple divisions of a spherical cell (5 – 6 – 6.5 μm in diameter) with homogenous content, released from the top of a claviform cell after its single transversal division. Free-floating in the phytoplankton of a small tropical lake.','Stoyneva-Gärtner et al. 2021',NULL,0,0),(2329,2477,'etymology','The species epithet <em>kitagatae </em>refers to the first locality, where the species was found – tropical crater lake Kitagata (Uganda, Africa).','Stoyneva-Gärtner et al. 2021',NULL,0,0),(2330,2478,'description','Populations of <em>Cyanocohniella rudolphia</em> sp. nov. show a polymorphic life cycle. This species forms bright green to blue-green heterogeneous mats on agar associated with a liquid and slimy mucilage. The adult and main form resemble <em>Nodularia</em>-like structures with straight, constricted and parallel always arranged uniseriate filaments embedded in a non-lamellated, fine and colorless sheath. During this stage, cells are rounded to ellipsoidal, flattened at the cross walls, 3–4.5 m long, 2.8–3.5 m wide. In addition, the uniseriate filaments can also become densely curved, resembling a Nostoc-like morphology embedded in a well-pronounced, non-lamellate, hyaline sheath of up to 13 m thickness. At this stage, cells are smaller than those of the Nodularia-like stage, isodiametric with a diameter of 2.1–3.5 m. Heterocytes also are present on nitrogen-containing medium, which are ellipsoidal and wider (3.8–5.3 m) than long (3–4 m) and intercalary. Akinetes are formed during the <em>Nodularia</em>-like stage in uniseriate series as oval, mostly granulated blue-green to brown cells with a thick cell wall that can be up to 7.5 m long and 4.1 m wide and can sometimes be surrounded by a massive sheath layer. After serial akinete formation, the uniseriate akinete containing filaments detach. From the akinetes young filaments or motile hormogonia develop that show a Pseudanabaena/Leptolyngbya-like morphology with constricted cells that are cylindrical and 2.4–3.8 m long and 2.7 m wide. The apical cells of these filaments are longer (up to 5.3 m) than wide (2.7 m) and conical. During this stage, cells are granulated. Cell division takes place in one plane during all stages. Thylakoid position is coiled as the cell content is homogeneously distributed across the mostly non-granulated blue-green cells.','Jung et al. 2022',NULL,0,0),(2331,2478,'etymology','‘<em>Rudolphia</em>’ is the name of the respective potash pit ‘Schacht Rudolph’, belonging to the former potash works ‘Teutonia’, Schreyahn.','Jung et al. 2022',NULL,0,0),(2332,2479,'description','Filaments slightly intertwined, containing one or multiple trichomes. Sheaths colorless, lamellated, firm or diffluent, thick, attached to or separated from trichomes. Trichomes bluegreen to gray-green, attenuated ends, constricted at crosswalls, gliding motility, unbranched. Cells shorter than wide, circular in cross-section. Apical cells beak, rounded, sharp, pointed, without calyptra, not capitate. Thylakoid pattern parietal to the irregular, with a central fascicle arrangement. Reproduction with frequently long hormocyte or sometimes fragmentation by necridic cells.','Lee et al. 2022',NULL,0,0),(2333,2479,'etymology','Edaphophycus is derived from ‘edaphos’ (Greek), which means bottom or soil, and ‘phykos’ (Greek), which means alga.','Lee et al. 2022',NULL,0,0),(2334,2480,'description','In a natural sample, each trichome is wrapped in the sheath or numerous trichomes are enclosed in the mucilage (Figs 2–5). Filaments entwined and twisted, containing one to multiple trichomes. Sheaths colorless, lamellated, firm or diffluent, thick. Trichomes blue-green to gray-green, attenuated ends, constricted at cross-walls, gliding motility, unbranched. Cells shorter than wide, frequently isodiametric, circular in cross-section (1.22) 1.44–4.31 (4.82) μm long. Apical cells beak, rounded, sharp, pointed, sometimes hemispherical, without calyptra, not capitate. Thylakoid pattern parietal to the irregular, with a central fascicle arrangement. Reproduction with frequently long hormocyte or sometimes fragmentation by necridic cells.','Lee et al. 2022',NULL,0,0),(2335,2480,'etymology','‘Epilithus’ means ‘on the surface of a rock’','Lee et al. 2022',NULL,0,0),(2336,2481,'description','Thallus in desert soils microscopic, on Z8 agar dark blue-green, consisting of numerous globular to irregularly shaped microcolonies, in liquid Z8 media forms a dark blue-green mat consisting of numerous microcolonies, with a few erect aggregates of microcolonies. Microcolonies in culture with cells densely packed, with trichomes not evident in globular colonies, thinner filamentous colonies appearing 1–4 cells wide and several times longer than wide, larger colonies subspherical. Mucilage colorless, thin, with a firm outer layer. Trichomes 3.5–6.5 um wide, disarticulating to produce masses of solitary cells (monocytes). Hormogonia and hormocytes not observed. Vegetative cells spherical, oval, or irregular when closely appressed to neighboring cells, as long as wide or shorter than wide, 4.2–6.0 um long, 3.5–6.5 um wide in uniseriate filaments, becoming up to 8.3 um long and 10.3 um wide in multiseriate filaments. Apical cells often bluntly conical. Heterocytes very rare, 4.2– 6.3 um long, 4.2–6.7 um wide. Akinetes largest cells, without notable epispores, non-granular. At 4 weeks after transfer onto solid media producing numerous gold-colored senescent cells.','Baldarelli et al. 2022',NULL,0,0),(2337,2481,'etymology','Named in honor of Lorgio Aguilera, who was of great assistance during our field sampling in the Atacama Desert.','Baldarelli et al. 2022',NULL,0,0),(2338,2481,'diagnosis','Similar to <em>M. pulchra</em> and<em> M. dolomitestris</em>, differing in the ability to produce bluntly conical end cells and abundant enlarged cells in multiseriate filaments.','Baldarelli et al. 2022',NULL,0,0),(2339,2482,'description','Thallus in desert soils microscopic, on agar dark green to blue-green. Colonies forming globular, oval, to irregular-shaped growths on agar, colonies spread mostly flat on agar medium eventually forming large colonies rising well above the surface of the Petri dish, in liquid no erect aggregates of microcolonies observed but attaches as microcolonies to glass surfaces. Microcolonies in culture with cells very densely packed, with trichomes not evident in globular colonies, at first composed of uniseriate filaments, producing few multiseriate filaments, in older cultures dominated by larger elongated colonies with numerous densely packed cells. Mucilage at first colorless, developing into a firm thick sheath early in the life cycle (2 weeks), mucilage turning partially yellow-brown or yellow-pinkish 1 month after transfer and becoming compartmentalized around dissociated cells. Trichomes 3.0–7.5 um wide, with subspherical apical cells. Cells pale green to blue-green to bright bluegreen when actively growing, when old, yellow-green to yellow, with centroplasm less pigmented when mature, 2.5–6.0 um long. Akinetes enlarged spherical to subspherical cells in uniseriate filaments, up to 7.5 um wide, germinating to produce solitary monocytes. Heterocytes not observed. Monocytes numerous in 1-month-old cultures, 6–8 um in long.','Baldarelli et al. 2022',NULL,0,0),(2340,2482,'diagnosis','Similar to <em>Mojavia aguilerae</em>, but with firm, colorless to yellowish, compartmentalized mucilage and enlarged, nearly spherical akinetes. Similar to <em>M. pulchra</em>, but with more densely packed microcolonies, the rarity of brownish sheath pigmentation, and the absence/rarity of heterocytes.','Baldarelli et al. 2022',NULL,0,0),(2341,2482,'etymology','Dolomitis (L.) = dolomite limestone, and –estris (L.), a suffix meaning “living in.” Growing in soils derived from dolomite.','Baldarelli et al. 2022',NULL,0,0),(2342,248,'description','Colonies are microscopic and free-living in desert soils. On agar, macroscopic colonies start as conglomerations of small, spherical to lobate colonies, which remain distinct throughout the life cycle. Even old colonies consist of aggregations of microcolonies, and form fairly flat masses on the agar surface (Fig. 7B). Macrocolonies start dark green, and become yellowgreen to gray green. Microcolonies are rounded, irregular, not becoming macroscopic, averaging 40–45 um long by 30–35 um wide. Sheaths are thin, firm, and colourless in young colonies, with trichomes lying less than 4 um from the outer surface, becoming brownish yellow and compartmentalized in older colonies. Trichomes are unrecognizable in the younger colonies, becoming visible but still very compact after one month of growth, curved and bent, 2–7 mm wide. Hormogonia with oval to quadratic compressed cells are 2–6 um long by 2–5 um wide. Vegetative cells are rounded to irregularly compressed in compact colonies before trichomes are visible; in the trichome they are usually barrel-shaped to oval, or quadratic after division, constricted at the cross-walls, 2–7 um long by 2–7 um wide. Heterocytes are oval to rounded, intercalary or apical in position, 3–8 um long by 2–8 um wide. Akinetes are round to oval, intercalary to apical in position, with smooth to granular surface, yellowish, 6–11 um long by 5–11 wide.','Řeháková et al. 2007',NULL,0,1),(2343,2483,'description','Colonies are microscopic and free-living in desert soils. On agar, &nbsp;macroscopic colonies start as conglomerations of small, spherical to &nbsp;lobate colonies, which remain distinct throughout the life cycle. Even &nbsp;old colonies consist of aggregations of microcolonies, and form fairly &nbsp;flat masses on the agar surface (Fig. 7B). Macrocolonies start dark &nbsp;green, and become yellowgreen to gray green. Microcolonies are rounded, &nbsp;irregular, not becoming macroscopic, averaging 40–45 um long by 30–35 um &nbsp;wide. Sheaths are thin, firm, and colourless in young colonies, with &nbsp;trichomes lying less than 4 um from the outer surface, becoming brownish &nbsp;yellow and compartmentalized in older colonies. Trichomes are &nbsp;unrecognizable in the younger colonies, becoming visible but still very &nbsp;compact after one month of growth, curved and bent, 2–7 um wide. &nbsp;Hormogonia with oval to quadratic compressed cells are 2–6 um long by &nbsp;2–5 um wide. Vegetative cells are rounded to irregularly compressed in &nbsp;compact colonies before trichomes are visible; in the trichome they are &nbsp;usually barrel-shaped to oval, or quadratic after division, constricted &nbsp;at the cross-walls, 2–7 um long by 2–7 um wide. Heterocytes are oval to &nbsp;rounded, intercalary or apical in position, 3–8 um long by 2–8 um wide. &nbsp;Akinetes are round to oval, intercalary to apical in position, with &nbsp;smooth to granular surface, yellowish, 6–11 um long by 5–11 wide.','Řeháková et al. 2007',NULL,0,0),(2344,248,'description','Cyanobacterial genus similar to the genus Nostoc. Colonies microscopic in nature, subsphaerical, ellipsoid to irregular, surrounded by a firm and mucilaginous covering. Series of subcolonies create macroscopic, upright or horizontal pseudofilaments in liquid culture. Cells subsphaerical, joined into uniseriate trichomes or strongly flexuous pleuroseriate colonies, strongly constricted at the crosswalls, or agglomerated into dense &nbsp;aggregations. Heterocytes mainly terminal, or lateral in agglomerations, with intercalary heterocytes very rare. Young colonies only with terminal heterocytes. Reproduction with colonial disintegration, by free solitary cells (hormocytes) or multicelled hormogonia. Hormogonia germinating without heterocytes, often with intercalary paired widened cells which often cause acute bending of the hormogonia.','Řeháková et al. 2007',NULL,0,0),(2345,2486,'description','Filaments formed mats in liquid culture, often attached to the bottom or floating on the surface (Fig. 1). Filaments were isopolar, solitary, lacked heterocysts, or were coiled into clusters and mats. Filaments were purplish-brown under white light but became grass green under far-red light. Filaments were formed by individual trichomes joined by thin and colorless sheaths. Individual trichomes were fine, cylindrical, usually did not attenuate at their ends, had rounded apical cells, and had slight constriction at crosswalls. Cells were 0.93–2.17 μm long and 1.14–1.31 μm wide and were slightly smaller with a much thicker sheath under far-red light compared with those under white light. Cells had four to six parietal thylakoid membranes and occasionally had slightly darker prominent granules.','Shen et al. 2022',NULL,0,0),(2346,2486,'etymology','The specific epithet “minuta” refers to the smaller cell size of <em>Kovacikia minuta</em> compared to <em>K. muscicola</em> HA7619-LM3.','Shen et al. 2022',NULL,0,0),(2347,2491,'description','Colonies purple blue-green; young colonies up to 0.1 mm diameter, solid, developing into mature colonies up to 10 mm diameter, consisting of a membranous sheet folded into a somewhat cerebriform, hollow sac. Cells cuboid to spherical and ellipsoidal, either very regularly arranged in cubical patterns in 3-5 layers or with different degrees of a less regular, radiating pseudo filamentous arrangement in up to 12 layers; increasing<br>in size away from the colony surface, the increase being up to 20-fold in colonies with regular cell arrangement and four-fold in colonies with the least regular cell arrangement; outer cells from 1.5 um in diameter; innermost cells up to 30 um in diameter. Inner enlarged cells can become markedly vacuolate with a single massive vacuole almost entirely filling the largest cells. Mucilage between neighbouring cells is 1-5 um thick, colourless, firm, mostly homogeneous but occasionally faintly lamellate. Reproduction by release of single cells from the colony surface.','Broady &amp; Ingerfeld 1991',NULL,0,0),(2348,2494,'description','On solid media, colonies are irregular, dark brown in color with no distinct periderm. In liquid media, filaments form small clusters that are loosely attached to the bottom of the flasks. Filaments are long and flexuous (Figure 1C), sometimes forming irregular clusters, rarely interwoven (Figure 1A) with variable tendencies for coiling (Figure 1C,D). Sheaths are colorless, very thin, visible after staining with Indian ink (Figure 1H). Trichomes uniseriate, isopolar, without false branching, constricted at the cross-walls, non-motile (Figure 1C–H). Vegetative cells are cylindrical with rounded ends, oval or barrel-shaped (3.3) 3.5–6.6 um long and 2.6–3.5 um wide, brown in color with smooth and finely granulated content. Apical cell rounded. Very slightly tapered terminal cells were sometimes observed. Heterocytes in terminal and intercalary positions, mostly solitary, rarely up to three in a row with yellow–green homogenous content (Figure 1C,E–H). Terminal heterocytes almost spherical to spherical (3.0) 3.2–5.0 (5.6) um in diameter, and cylindrical with rounded ends to oblong 3.9–5.9 um long and (3.2) 3.4–4.0 um wide. Intercalary heterocytes cylindrical with rounded ends or cylindrical to oval (4.2) 4.4–7.0 (7.4) um long and (2.8) 3.1–5.0 (5.7) um wide or almost spherical to spherical 3.6–5.0 (5.7) um in diameter. Akinetes develop in rows (Figure 1I,J). Fully developed akinetes appear spherical to oval, with dark green color, up to 12 m wide. Motile hormogonia with gas vesicles bearing terminal heterocytes were occasionally observed (Figure 1K).','Christodoulou et al. 2022',NULL,0,0),(2349,2494,'etymology','al.ka.li0phi.lum. N.L. n. alkali (from the Arabic word ‘alqali’, ashes of salt wort); N.L. adj. philus -a -um (from Gr. masc. n. philos, friend); N.L. neut. adj. alkaliphilum, friend of alkaline environments.','Christodoulou et al. 2022',NULL,0,0),(2350,2496,'diagnosis','Most similar to <em>Leptolyngbya </em>sensu stricto such as thin and untapered trichome with colorless sheath but with distant phylogenetic position based on 16S rDNA and rpoC1 gene sequences. Differs from the sister genus/clades ecologically in its occurrence in a cyanobacterial mat on tropical surface soil and morphologically by being wider and longer with a frayed sheath appearance.','Tawong et al. 2022',NULL,0,0),(2351,2496,'description','Filaments straight, flexuous, loosely entangled, frequently single or double false branching. Trichomes with a parietal arrangement of thylakoids (distinguishable centroplasm and chromotoplasm), slightly constricted or nonconstricted at the cross wall, gray-green to reddish content in healthy trichomes becoming orangebrown to green-yellow in older trichomes. Older trichomes wider than younger trichome. Cells shorter than width to longer than width in the same trichome. Sheath colorless, fine, often forming a frayed appearance along the middle part or at branching region of the filament. Reproduction via hormogonia. Necridic cells present.','Tawong et al. 2022',NULL,0,0),(2352,2496,'etymology','Siam in Latin is the old name for Thailand, referring to the locality where the organism was isolated, while capillus in Latin means thread or filament.','Tawong et al. 2022',NULL,0,0),(2353,2497,'diagnosis','Species separated by morphology, molecular and phylogenetic analyses based on 16S rDNA, 16S–23S rDNA ITS region, and rpoC1 gene sequences. Unique structures of D1–D1′, V2, Box-B, and V3 helices among all cyanobacteria in the Oculatellaceae for which ITS structure analyses have been reported.','Tawong et al. 2022',NULL,0,0),(2354,2497,'description','In environmental material, filaments were blue-green with a parietal longitudinal arrangement of thylakoids along the trichome, sometimes with multiple granule content and entangled with other filamentous cyanobacterial genera, i.e. Scytonema C.Agardh ex É.Bornet &amp; C.Flahault (1886:86), forming biocrusts or biofilms on soil surfaces. In culture material on solid agar, macroscopic colonies formed fascicles of filaments, with reddish to orange-brown, flat facultative growth. In liquid culture material, filaments gray green-reddish to orange-brown and becoming yellow-green with age, cotton ball-like forming floating with oxygen bubbles during photosynthesis, sometimes as tufted filament attached to tube surfaces. Filaments straight, flexuous, sinuous, sometimes spiral and coiled, often with a loop, loosely entangled forming fascicles, 2.8–4.6 μm in width (average 3.9 μm), frequently single and double false branching, sometimes bent at ends. Sheaths firm, thin, colorless, frequently frayed appearance along the middle part or at the branching regions of the filament, open or closed at the end, with one trichome per sheath. Trichomes untapered, slightly constricted or unconstricted at the distinctly visible cross-wall, with parietal longitudinally arranged fascicles of thylakoids along the inside walls. Vegetative cells mostly gray to blue-green, brown, various shape, shorter than width to longer than width the same trichome, 1.5–5.1 μm length (average 3.0 μm), 1.9–3.9 μm in width (average 3.0 μm), 0.5–2.0 in length to width ratio (average 1.0), with distinct chromatoplasm and centroplasm, parietal thylakoid, regularly nongranular cell content, sometimes with one or multiple granules visible in older cells. Apical cells cylindrical with rounded apices. Hormogonia simple fragmentation, often with 6–14 cells. Necridia cells single or often in rows at up to 7 μm long. Reproduction by fragmentation at necridia cells and<br>hormogonia. Phycoerythrin (54.11%) as the dominant phycobiliprotein pigment, with maximum spectral peak at 566 nm.','Tawong et al. 2022',NULL,0,0),(2355,2497,'etymology','<em>rubidus </em>in Latin means reddish referring to the dominant pigment phycoerythrin and color of filament in the exponential growth phase','Tawong et al. 2022',NULL,0,0),(2356,2498,'description','Colonies (thallus) spreading, mounded, in cultures growing as big bubbles (Fig. S1) with a firm trichome layer (Fig. 9B), blue-green, dark green. Sheaths absent. Trichomes cylindrical, straight, not capitate, motile with intense gliding in the direction of the longitudinal axis, sometimes accompanied by bending and distinctive rotation, 1–3 μm wide. Cells usually 2–4 longer than wide, 4–8 μm long, sometimes with visible parietal chromatoplasma, sometimes with evident cyanophycin granules (Fig. 9C-E), without aerotopes, after division growing to the size of the mother cells before the next cell division (Fig. 5E). Apical cells in developed trichomes bent, narrowed, rounded or pointed-rounded, never calyptrate or capitate. Thylakoids parietal (Fig. 9D-E), with triangle or rhombic organization in the transversal section (Fig. 9B).','Jasser et al. 2022',NULL,0,0),(2357,2498,'etymology','The genus name refers to Anna Hillbricht-Ilkowska (1930–2021), a distinguished Polish limnologist whose research concerned productivity models of freshwaters, plankton succession as well as landscape ecology concept and holistic approach in limnological studies.','Jasser et al. 2022',NULL,0,0),(2358,2499,'description','Colonies (thallus) spreading, mounded, in cultures growing as big bubbles (Fig. S1) with a firm trichome layer (Fig. 9B), blue-green, dark green. Sheaths absent. Trichomes thin, bright blue-green, usually straight or slightly bent, dispersed evenly and loosely without mat formation, indistinctly or slightly constricted at the cross<br>walls (Fig. 9A-B), 1.8–3.2 μm wide, slightly attenuated and bent at the ends, motile with gliding motility. Cells pale olive-green to bright bluegreen, with huge cyanophycin granules at the cross walls (Fig. 9C-E), 2–4 × longer than wide, 3.8–7.9 μm long. Apical cells (developed) cylindrical, rounded and elongated. Necridic cells not observed. Thylakoids parietal, with generally straight four to five layers of thylakoid membranes (Fig. 9C-D). Thylakoids in transversal section with triangle or rhombic organization (Fig. 9C). Numerous polyphosphates and carboxysomes of variable size were found, mainly at the parietal part of the cells (e.g., Fig. 9C-E).','Jasser et al. 2022',NULL,0,0),(2359,2499,'etymology','The specific epithet refers to the Pamir Mountains, which lie mostly in the Gorno-Badakhshan Province of Tajikistan from where the strain was isolated.','Jasser et al. 2022',NULL,0,0),(2360,2500,'description','Filaments mostly solitary, at times with multiple hormogonia in a common sheath, or with loose nodule formation (Fig. 7AB). Sheath clear, thick and widened, three to four layers (Fig. 7C-D). Trichomes straight, flexuous, or entangled within a sheath into a loose nodule, sometimes spirally coiled, slightly constricted at the cross walls, with slow gliding motility observed in trichomes lacking sheath, not tapered. Cells mostly shorter than wide, becoming isodiametric to slightly longer than wide before division, without aerotopes, sometimes with cyanophycin granules in cytoplasm (Fig. 7A-B); with parietal thylakoids. Apical cells rounded, without calyptra. Reproduction by trichome fragmentation via disintegration at necridia (Fig. 7A,C,E).','Jasser et al. 2022',NULL,0,0),(2361,2500,'etymology','The genus name is made of the Homeric ancient Greek word ἀμφίρυτος (amphírytos) meaning literally flowed around, surrounded everywhere by water.','Jasser et al. 2022',NULL,0,0),(2362,2501,'description','Colony bright blue-green (Fig. 7A-B). Filaments long or short, loosely to tightly spirally coiled, rarely singly, 2.0–6.0 μm wide. Sheath firm, colorless, usually attached to the trichome, occasionally softer, widened, sometimes irregular and stratified. Trichomes untapered, more or less constricted at the distinctly visible crosswalls, occasionally with tight, regular, screw-like coils, necridia observed, 1.5–2.5-(3.0) μm wide (Fig. 7A,C,E). Cells slightly shorter than wide to longer than wide, with one to two granules, with parietal thylakoids, 1.0–3.0 μm long (Fig. 7D). End cells rounded. Necridic cells are formed both intercalary and in terminal cells.','Jasser et al. 2022',NULL,0,0),(2363,2501,'etymology','The specific epithet refers to the ability of the species to form necridic cells; from the Greek νεκριδικός (necridicos).','Jasser et al. 2022',NULL,0,0),(2364,2502,'description','Filaments forming expanded blue-green mats (Fig. 8AB) on the substratum and large floating mucilaginous mats in older liquid cultures (Fig S1). Variously curved, flexuous, densely packed, isopolar trichomes, with rounded apical cells. Each trichome is individually surrounded by a thin colorless sheath (Fig. 8C-E). Cells longer than wide (1.2–3.2 μm long and 0.7–1.1 μm wide) with slightly or not visible constrictions at the cross walls. Homogeneous cell content and lack of gas vesicles. Reproduction by trichome fragmentation into short hormogonia without necridia (Fig. 8A). Cell division always symmetrical, perpendicular to the longitudinal axis of the trichome, and daughter cells dividing and growing to the size of the mother cell before the next division. Slow gliding motility. With TEM, 3–4 parietal thylakoids, and a multilayered thin sheath approximately (Fig. 8C-E).','Jasser et al. 2022',NULL,0,0),(2365,2502,'etymology','The specific epithet refers to František Hindák (1937–2019), a noted Slovakian phycologist who carried out intense research on the biology and taxonomy of green algae and cyanobacteria and established more than 90 algal taxa.','Jasser et al. 2022',NULL,0,0),(2366,2503,'description','<strong>Macroscopic view of the mats in the field:</strong> Thallus was fine, soft, disintegrating, brown with slight purple hues, sometimes dark olivegreen to almost black, periphytic in streams, forming large mats on the top of mud and other soft substrata, and often twisted around underwater branches and plant roots (Fig. 6 A–B). Mats were only loosely attached to the bottom surface, and thus easy removable.&nbsp;<br><strong>Microscopic view in environmental conditions:</strong> Filaments were up to 5 mm long, flexible, slightly and irregularly curved, sometimesspirally-coiled, loosely entangled within a mat; olive-green, violet or brown (Fig. 6 C). Thin colorless sheaths were observed infrequently at the end of the filaments (Fig. 6 D), but they were not consolidated to support a gelatinous, mucilaginous mat. Filaments were motile, with trembling, gliding and slight rotation, but oscillation and clockwise rotation was not observed; often single long motile filaments were<br>creeping within the mucilage of green algae and other cyanobacteria. Trichomes were slightly attenuated at the straight apex in some cells. Cell diameters ranged from 5 to 9 μm wide, 2.8–4.5 μm long, rarely isodiametric (longer than wide during cell division only), and not constricted at the often granulated cross walls (Fig. 7 A, C, E). Apical cells capitate, 4.3–5.9 μm wide, with typically rounded, but sometimes truncated calyptra.<br><strong>Microscopic view in culture conditions</strong>: strain PTRS2 in BG-11 culture conditions shows trichomes brown, brownish-greenish, sometimes purple or yellowish, with gliding movement, long, flexuous, rarely straight, not attenuated or so at the apex (1–3 apical cells may be elongated and narrowed), which was straight, not hooked (Fig. 7 B). Cells were 4.4–7.5 μm wide, 2.8–4.1 μm long, shorter that wide, rarely isodiametric (longer than wide during cell division only), not or sometimes slightly constricted at typically granulated cross walls. Apical cell capitate, 3.1–5.4 μm wide, with typically rounded, but sometimes truncated calyptras (Fig. 7 B, G). Sheath lacking or thin at the end of trichomes with actively dividing, thicker and diffluent in old cultures with short cells in stationery phase, colorless. When cultured in BG-11(-N), after 20 days of N-starvation, many cells were keritomized, (e.g., “vacuolized” and with “net-like” protoplast) caused by possibly widened thylakoids (Fig. 7 I). In both BG-11 and BG-11 (-N) many filaments disintegrated in hormogonia by help of necridic cells after 20<br>days of culturing (Fig. 7 H and I).','Conklin et al. 2020',NULL,0,0),(2367,2503,'etymology','The species epithet refers to the anatoxin-a production of this species, persisting in culture conditions to date four years after its isolation.','Conklin et al. 2020',NULL,0,0),(2368,2504,'description','Unicellular thallus is extended, compact, irregular in shape, and composed of numerous colonies or isolated ensheathed cells. The colonies on agar are blue-green, single, irregularly rounded, and of various sizes that aggregate to bigger uneven structures that become olive green to light brown when old. The cells aggregate into larger, loose clusters, with various single cells tightly encapsulated in a common sheath when young. Within these smaller packets, the young cells are oval to ellipsoid but slightly geometrically and vivid blue-green, with longitudinal diameter of 2.4–2.8 and transverse diameter of 1.4  0.2 um. It forms mostly single cells that are loosely embedded in a common sheath during aging and that are mostly rounded and only sometimes slightly ellipsoidal, 3.5–4.5 um in diameter and pale blue-green, and surrounded by a hyaline, diffluent to sometimes limited sheath. Solitary cells without sheath were rarely observed. Cell content is mostly homogeneous, sometimes slightly finely granulated with parietal thylakoid position. The sheath is up to 5 mm wide, hyaline, sometimes lamellate, limited, and not following the shapes of the cells but rather rounded. Reproduction is by simple binary cell division in three or more planes and forms baeocytes by successive fission containing up to hundreds of cells in a common sheath; nanocytes were not observed. The cells are not motile and were not able to grow on BG 11 medium without nitrogen.','Jung et al. 2021',NULL,0,0),(2369,2504,'etymology','<em>Compacta</em>—from Latin “compact” due to the smaller packets comprising various compressed cells.','Jung et al. 2021',NULL,0,0),(2370,2505,'description','It is unicellular. The colonies on agar are brownish on the outside but greenish to blue-green in the inside, single, regularly rounded, and emerging up to 3 mm from the agar. It forms rounded balllike cell clusters of blue-green color in liquid cultures and which do not float. The cells aggregate into larger, limited clusters, with various single cells tightly, but never compressed, encapsulated in a common sheath. The aggregates are rounded to spherical when young but enlarge to irregularly rounded patches during aging. The cells are oval, vivid blue-green with a longitudinal diameter of 4.8–5.3 um and with a transverse diameter of 3.0–3.2 um. The cells from the outer periphery of large colonies are brownish. The sheath is hyaline, firm, and limited but turns yellow to brown during aging or at the periphery of older, macroscopic colonies. The sheath capsules of single cells embedded in cell clusters are frequent; here the sheath is firm and strictly limited, forming a capsule. Solitary cells without sheath were frequently observed in case of deliberated cells. The cell content is mostly homogeneous, sometimes slightly finely granulated, with hyaline granules positioned at the outer periphery of the cells and with parietal thylakoid position. Reproduction is by simple binary cell division in three or more planes, forming baeocytes by successive fission containing up to hundreds of cells embedded in a common sheath; nanocytes were not observed. The cells are not motile and were not able to grow on BG 11 medium without nitrogen.','Jung et al. 2021',NULL,0,0),(2371,2505,'etymology','<em>Gigantea</em>—from Latin “gigantic” due to the big cells compared to other known <em>Aliterella </em>species.','Jung et al. 2021',NULL,0,0),(2372,2506,'description','It is unicellular. Young single colonies on agar are slimy and diffluent, which combine into comprehensive, flat, and slimy biofilms, forming thick, rigid, flake-like aggregates of vivid green color during aging. The unicellular cells irregularly aggregated, but not squeezed, in dense colonies with irregular round to elongated cells that are curved when elongated, with longitudinal diameter of 4.1–4.3 um and transverse diameter of 1.9–2.7 um. The sheath is variable but always colorless, tight, and not lamellate; it is diffluent when forming large colonies, limited, and rigid, forming smaller round cell packages, turn capsule-like when comprising single cells or two cells and absent in single cells and freshly released or liberated cells; the sheath turns yellow in old cultures. The cell content is mostly homogeneous, sometimes slightly finely granulated to granulated when older, with parietal thylakoid position. Reproduction is by simple binary cell division in three or more planes, forming baeocytes by successive fission containing up to hundreds of cells embedded in a common sheath; nanocytes were not observed. The cells are not motile and were not able to grow on BG 11 medium without nitrogen.','Jung et al. 2021',NULL,0,0),(2373,2506,'etymology','Ellipsoidea—from Latin “elliptical,” describing the curved longitudinal shape of the cells.','Jung et al. 2021',NULL,0,0),(2374,2507,'description','This is unicellular. It forms macroscopic rounded, balllike baeocytous colonies in liquid culture and thick &nbsp;threedimensional layers on agar. The cells are large compared to other Chroococcidiopsidales, up to 8 um; the single cells are polygonal but mostly tightly pressed against each other in rounded colonies of a few dozens of cells held together by a very firm, rigid, colorless, and limited sheaths. Reproduction by simple binary cell division in three or more planes; baeocytes or nanocytes were not observed.','Jung et al. 2021',NULL,0,0),(2375,2507,'etymology','<em>Pseudocyanosarcina</em>—This means that it looks like Cyanosarcina, a pleurocapsalean cyanobacteria genus that shares morphological features.','Jung et al. 2021',NULL,0,0),(2376,2508,'description','This is unicellular. It forms three-dimensional, rounded, baeocyte-like colonies of different sizes on agar when young and which aggregate into bigger clots of about 3-mm thickness. It forms dark green to blackish rounded structures of about 1–3 mm in diameter that do not float in liquid culture, without single cells swimming in the medium. The cells dyed in liquid medium (but not agar plates) were pinkish, probably due to the released phycocyanin granules of dead cells. It forms dense, rounded, bubble-like colonies that are tightly agglomerated, resembling baeocytes, comprising a few to several dozens of cells. The cells are blue-green to bright green, of irregularly rounded shape of (4.7) 5.8–6.1 (8.9) um in diameter and tightly pressed against each other within rounded colonies, very firmly held together by a limited, slightly lamellate, not diffluent, colorless sheath. Rarely observed are single cells of polygonal to rounded, ellipsoidal shape that mostly adhere to the bigger colonies and are unsheathed. The cell content is granulated, with a few small granules and bigger phycocyanin granules of up to 3 um that could be observed throughout a variety of tested media, light conditions, and temperatures using light microscopy (blue), simple polarized light (red), and under autofluorescence. The arrangement of the thylakoid membranes is lamellar and parietal, not filling out the whole cell. Reproduction is by simple binary cell division in three or more planes. The cells are not motile and were not able to grow on BG 11 medium without nitrogen.','Jung et al. 2021',NULL,0,0),(2377,2508,'etymology','Phycocyanin—the name of the blue pigment unique for cyanobacteria that can be found as granules in the cells.','Jung et al. 2021',NULL,0,0),(2378,2509,'description','The colonies on agar are rounded, rigid, and firm, forming blackish to dark green rounded balls of up to 3-mm diameter in liquid culture that do not float or disintegrate into single cells. The cells are always arranged in rounded to irregularly rounded structures surrounded by a rigid, strictly limited, and thick mucilaginous, hyaline, non-lamellate sheath. Within these up to macroscopic globose structures, rounded cells of 4.7–5.1 um in diameter form long, strictly uniseriate filaments, rarely with heterocytes. The ruptured sheaths release short, unsheathed hormogonia of similar morphology or short filaments made of only a few cells embedded in a thick, firm, non-lamellate, and hyaline sheath. The later type is often made of smaller cells that can be tightly pressed against each other. Oval heterocytes of 5.4–6.2 (6.8) um in diameter can rarely be observed, but their number drastically increases under nitrogen-depleted conditions within smaller packages of cells (praemordia) comprising a few dozen cells. The thylakoid membrane orientation is parietal in parallel stacks.','Jung et al. 2021',NULL,0,0),(2379,2509,'etymology','<em>Globosa </em>from Latin, which means “globose” due to the rounded form of the colonies that reach up to 3 mm in size.','Jung et al. 2021',NULL,0,0),(2380,2510,'description','The colonies on agar form a dense creeping, flat, irregularmat, growing radially from the center via hormogonia release, forming dull blue-green, loose flocks in liquid medium. Thecolonies are formed by (mostly single) cells surrounded by a limited, hyaline, sometimes slightly lamellate, sheath with short uniseriate filaments. Mostly, uniseriate short filaments are formed by only a few cells that are loosely connected that stretch out to praemordia-like aggregates comprising only a few dozen cells. Heterocytes are only visible under nitrogen-depleted conditions forming apical and within short rows of cells. The heterocytes are rounded or spherical, 5.3–5.4 um in diameter. The cells are round, 4.4–4.6 um in diameter, dull blue-green, finely granulated, and have a characteristic vacuole-like structure centered in the cells. The thylakoid membrane orientation is parietal in parallel stacks.','Jung et al. 2021',NULL,0,0),(2381,2510,'etymology','<em>Gloeocapsoidea</em>—from Latin “looks like <em>Gloeocapsa</em>” due to the morphology of the adult stage resembling <em>Gloeocapsa</em>.','Jung et al. 2021',NULL,0,0),(2382,2511,'description','Filaments uniseriate, isopolar when in early growth stage, becoming heteropolar upon fragmentation mid-filament, and mucilaginous. Sheath absent or thin, transparent, and diffluent. Heterocytes terminal, developing prior to akinete formation, sometimes intercalary. Proakinetes elongated. Akinetes paraheterocytic, distinctly larger than vegetative cells and heterocytes.','Pal et al. 2022',NULL,0,0),(2383,2511,'etymology','<span data-field=\'authority\' data-froala=\'light\' data-harvest=\'froala\' placeholder=\'Type something\'><em>Johanseniella </em>(Jo.han.se.ni.el’la. N.L. fem. n. <em>Johanseniella</em>, &nbsp;named in honor of well-known phycologist Professor Jeffery R. Johansen &nbsp;for his contributions tomodern taxonomy and inspiring an entire &nbsp;generation of taxonomists.).</span>','',NULL,0,0),(2384,2512,'description','Thick bluish-green mat on soil surface growing adjacent to a paddy field. Shiny, clumped, bluish-green colored mat in liquid medium.On a plate, colonies appearmucilaginous, firstly discrete, greenish, radial, or star-like, spreading from the center and later forming greenish, nonhomogenous and flat mat, older colonies turn yellowish and then brownish at later stages, elevation remains flat. Under the microscope, trichomes appear green in color, numerous, uniseriate, isopolar, loosely tangled, long, and straight, sometimes flexuous, without any sheath and remain in fascicles. Vegetative cells cylindrical, longer than wide, constricted at ends, sometimes granulated, and terminal cells crescent-shaped. Size of the vegetative cells in intercalary and terminal positions ranges from 1.83 to 3.97 μm long and by 1.42–2.22 μm wide and 2.15–3.92 μm long by 1.44–2.48 μm wide, respectively. Heterocytes always terminal, solitary, unipored, sometimes present at both ends of the filament, elongated, conical, or rarely narrowly oblong with blunt apices. Size of heterocytes ranges from 2.27 to 4.48 μm long and 1.67 to 2.47 μm wide. Reproduction via hormogonium formation and akinetes. Akinetes solitary, larger than most vegetative cells, formed adjoining to the terminal heterocyte at one end only,<br>shape and size vary majorly, some are narrowly oblong to oval and elliptical with sometimes one side more curved than another, mature akinetes granulated whereas younger proakinetes appear nongranulated and elongated, length varies from4.98 to 11.21 μm and width 3.99 to 5.64 μm. Epispore smooth, covered with a very thin transparent layer of mucilage. Hormogonia formed by fragmentation of filament or by degeneration of vegetative cells; aerotopes not observed.','Pal et al. 2022',NULL,0,0),(2385,2512,'etymology','<em>tripurensis </em>(tri.pu.ren’sis. N.L. fem. adj. tripurensis, pertaining to Tripura, from where the sample was collected).','Pal et al. 2022',NULL,0,0),(2386,2513,'description','Cells brownish colored; filamentous; coiled or tangled filaments; sheath colorless, very thin, not lamellate; trichome slightly constricted and composed of cylindrical, elongated cells; narrow trichome; apical cells are round; cells longer than broad; no false branching (Figure 4A). Trichomes unbranched and composed of cylindrical, elongated cells, 1.2–1.8 um in length and 0.8–1.1 um in width. Cross-walls of the cells contained constrictions (Figures 4B,C). Centripetal invagination of the cell wall divided individual cells, and intracellular connections between vegetative cells were not present (Figure 4C). Five to six thylakoids in the parietal arrangement were located parallel at the cells’ inner periphery. Sheath, septum, phycobilisome, carboxysomes, cyanophycin granule, lipid droplets, and polyphosphate bodies were all present in the cytoplasm (Figures 4C,D).','Tang et al. 2022',NULL,0,1),(2387,2513,'etymology','“Lepto” exhibiting morphology typical to the members of Leptolynbyaceae family, “thermo” similar to thermophilic (high temperature tolerant), “fonsia,” genus epithet derived from the Latin word fons meaning spring, since both representative of the genus to date, i.e., E412 and Greenland 10, are hot spring isolates;','Tang et al. 2022',NULL,0,0),(2388,2514,'description','Cells brownish colored; filamentous; coiled or tangled filaments; sheath &nbsp;colorless, very thin, not lamellate; trichome slightly constricted and &nbsp;composed of cylindrical, elongated cells; narrow trichome; apical cells &nbsp;are round; cells longer than broad; no false branching (Figure 4A). &nbsp;Trichomes unbranched and composed of cylindrical, elongated cells, &nbsp;1.2–1.8 um in length and 0.8–1.1 um in width. Cross-walls of the cells &nbsp;contained constrictions (Figures 4B,C). Centripetal invagination of the &nbsp;cell wall divided individual cells, and intracellular connections &nbsp;between vegetative cells were not present (Figure 4C). Five to six &nbsp;thylakoids in the parietal arrangement were located parallel at the &nbsp;cells’ inner periphery. Sheath, septum, phycobilisome, carboxysomes, &nbsp;cyanophycin granule, lipid droplets, and polyphosphate bodies were all &nbsp;present in the cytoplasm (Figures 4C,D).','Tang et al. 2022',NULL,0,0),(2389,2514,'etymology','“sichuanensis” species epithet derives from the name of collection province.','Tang et al. 2022',NULL,0,0),(2390,314,'diagnosis','Trichomata solitaria, libere natantia, brevia vel longa, circinata vel recta, plus minuusque constricta ad septa, cum vel sine vaginis mucosis, ad apices attenuata vel non-attenuata. Cellulae vacuolis gaseosis impletae, sphaericae vel cupiformes, post divisionem compressae. Heterocytae intercalares, solitariae, sphaericae. Akinetes plus minuusque sphaericae (proportio longitudo:latitudo 0.9–1.3), ad heterocytis utrinque vel unilaterale adjunctae. Planktice in aquis.','Zapomělová et al. 2009 (sub. Sphaerospermum)',NULL,0,0),(2391,314,'description','Trichomes of varying length, solitary, free-floating, coiled or straight, more-or-less constricted at the cell-walls, with or without mucilaginous sheaths. Terminal cells elongated and tapered or undifferentiated. Vegetative cells with aerotopes, spherical or barrel shaped, compressed during division. Heterocytes only intercalary, solitary, spherical. Akinetes spherical or nearly spherical (length:width ratio 0.9–1.3), from one or both sides adjacent to heterocytes. Planktonic in stagnant freshwater, rarely (secondary) in running waters.','Zapomělová et al. 2009 (sub. Sphaerospermum)',NULL,0,0),(2392,290,'description','Filaments solitary, free floating, without sheaths and gelatinous envelopes, straight, flexuous, or coiled. Trichomes uniserial, thin (&lt; 4 um in diameter) with or without constrictions at cross-walls, isopolar or subsymmetric, with or without heterocytes. If heterocytes present, only terminal, and oval, ovoid or conical, sometimes slightly curved and drop-like, unipored, and usually developed asynchronously at both ends of the trichome. Trichomes without heterocytes usually slightly attenuated toward both ends (or one end after trichome disintegration), apical cells conical-rounded or pointed but not elongated in cellular hair-like ends. Vegetative cells cylindrical or barrel-shaped, usually distinctly longer than wide, pale blue-green, yellowish or olive-green, facultative gas vesicles (aggregated in aerotopes). Akinetes solitary or in pairs, ellipsoidal or cylindrical, in coiled specimens usually slightly curved, usually developing distant from heterocytes, rarely adjacent to apical heterocytes. Reproduction by disintegration of trichomes and by akinetes.','Aguilera et al. 2018',NULL,0,0),(2393,2516,'description','Bluish-green mat on soil surface growing in a field covered with grass. Mucilaginous, gelatinous, light green coloured mats in liquid medium; in solid medium, colonies initially discrete to irregular in later stages of growth, mucilaginous with raised elevation, margin entire to somewhat undulate, soft textured, and light green. Under the microscope, trichomes appear light green, long, filamentous, numerous, loosely entangled, and young filaments less coiled than older filaments. Sheath difficult to distinguish. Vegetative cells barrel-shaped with some cells longer than width, terminal vegetative cells curved or crescent-shaped at the end, light-green coloured, granulated, and sometimes constricted, without aerotopes; intercalary vegetative cells range in size between 2.04 and 2.75 μm length and 1.74 and 2.06 μm width; terminal vegetative cells vary from length 2.13–2.70 μm to width 1.83–2.07 μm. Heterocytes spherical or oval to oblong in shape, both intercalary as well as terminal; intercalary heterocyte ranges in size from length 3.16–3.69 μm to width 2.55–2.99 μm; terminal heterocyte with length ranging from2.73 to 3.73 μm and width 2.38 to 2.93 μm. Reproduction via hormogonia formation and akinetes. Akinetes oval to oblong with variable ends, sometimes one side slightly curved, length varying from 3.59 to 4.02 μm and width 2.25 to 3.06 μm, epispore smooth, granulated, always formed adjacent to heterocyte, and found solitary or in pairs.','Pal et al. 2022',NULL,0,0),(2394,2516,'etymology','kailashaharensis (kai.la.sha.har.en’sis. N.L. fem. adj. kailashaharensis, pertaining to Kailashahar, a place in the state of Tripura, India, from where the sample has been isolated).','Pal et al. 2022',NULL,0,0),(2395,2517,'description','Epilithic or free–floating in spherical clusters. Thallus dark green to blue green, caespitose in the environment, fasciculate or not in culture. Filaments heteropolar, straight or flexuous, ± 2 mm long, 16.4–21.1 (19 ± 1.5) μm wide, with single or double false branching. Sheath hyaline, colorless, sometimes thick, lamellate and constricted, and sometimes expanded towards filament ends. Trichomes cylindrical, usually slightly to deeply constricted at cross–walls, 10.5–17.7 (14.5 ± 2.7) μm wide, very tapered only at the ends, usually ending in apical hyaline hairs. Cells in young developing trichomes (7.4–13.4 μm wide) are longer than wide, while older trichomes (10.5–17.7 μm wide) have discoid to flattened oval cell, always shorter than wide, 1.7–3.7 (2.4 ± 0.5) μm long; apical cells spherical, rounded to triangular, at times elongated to include several cells (±6) as seen throughout reproduction cycle. Cell content blue–green to forest green, finely granulated, cross–walls sometimes granulated. Heterocyte discoid, quadratic, cylindrical, basal or intercalary, in single (usually basal or intercalary) or serially intercalary in double, or triple, 8.8–17.3 μm length, 11–13 μm wide. Reproduction by monocytes released through vacuolized apical cells individually released from sheath or by isopolar or heteropolar hormogonia. Reproduction also facilitated by trichome fragmentation, with or without necridic cells, cell constriction or heterocyte breakup. Akinetes not observed.','Berthold et al. 2022',NULL,0,0),(2396,2517,'etymology','“<em>sanctimaloensis</em>” is to honor the French port, Saint–Malo, Ille–et–Vilaine, Brittany where the cyanobacterium was sampled','Berthold et al. 2022',NULL,0,0),(2397,2518,'diagnosis','Similar in morphology to <em>Calothrix</em>, <em>Dulcicalothrix</em>, and <em>Macrochaete</em>, but phylogenetically separate from those genera and with percent similarity of the 16S rRNA genes &lt;94.5% in comparison to other tapering genera.','Kumar et al. 2022',NULL,0,0),(2398,2518,'description','Filaments heteropolar, wider in the basal region, gradually tapering to the distal end, but not forming a terminal hyaline hair. Akinetes absent. Basal heterocytes present, with a senescent heterocyte often seen attached terminally to living heterocytes.','Kumar et al. 2022',NULL,0,0),(2399,2518,'etymology','Named in honor of U.S. Senator J. William Fulbright, a noted multilateralist in the mid-20th century who founded the Fulbright Fellowship Program, which supported the collaboration leading to this article.','Kumar et al. 2022',NULL,0,0),(2400,2519,'description','Colony macroscopically visible in small ponds, bluish-green to brownish, mucilaginous and shiny in appearance. Colony in laboratory-grown cultures on agar-solidified media in slants or Petri plates a bluish-green mat with shiny, mucilaginous texture. Colonies grown in low-phosphorous concentrations exhibiting less mucilage, more brittle texture, and less shiny appearance. Cultures grown in liquid media bluish green, with filaments adhering to each other rather than to the walls of the glass tubes. Filaments lacking a bulbous swollen base, gradually tapering from the base to the apex, when mature tapering to a non-hyaline trichome over 2 um wide, sparsely false branched, less than 20 um long in young filaments, over 200 um long in mature filaments. Sheath thin, firm, colorless, not lamellated and tightly bound to the cells of the trichome. Trichomes not too distinctly constricted at the cross walls, especially in basal regions, appearing less constricted in the long, thin terminal<br>regions of mature filaments, in basal region near heterocyte 2.3–5.1 um wide, in intercalary region 2.6–3.5 um wide, and in terminal region 2.2–3.2 um in wide. Vegetative cells prominently granulated, longer than wide or shorter than wide, 3.3–4.1 um long near the base, 2.6–6.2 um long in the main part of the trichome, becoming 2.1–4.7 um long near the terminus. Heterocytes terminal, basal in position, yellow in color, spherical or with clearly rounded free terminal ends and flattened to the adjacent vegetative cell, sometimes in pairs or series,<br>the newer cell subterminal to the older senescing heterocyte, 3.1–6.7 um long, 3.1–4.6 um wide. Necridia<br>present. Akinetes not observed.','Kumar et al. 2022',NULL,0,0),(2401,2519,'diagnosis','Morphologically most similar to <em>Calothrix clavata</em>, but differing in its smaller dimensions, particularly width of the basal region of the trichomes, which are 5–7 um wide in <em>C. clavata</em>. Differing from all other <em>Calothrix </em>species based on narrower trichome dimensions.','Kumar et al. 2022',NULL,0,0),(2402,2519,'etymology','Named in honor of Professor Yajnavalkya Bharadwaja (1895–1963), who received training with Prof. F. E. Fritsch and established the Banaras School of Phycology at the Banaras Hindu University. Prashant Singh is a fourth-generation member of this school, and we are pleased to honor this distinguished Indian phycologist.','Kumar et al. 2022',NULL,0,0),(2403,2520,'diagnosis','Similar to <em>Fulbrightiella bharadwajae</em>, but with wider trichomes, less tapering, and purplish cell color. Morphologically similar to <em>Calothrix elenkinii</em>, but much more constricted at the cross walls and purplish in color.','Kumar et al. 2022',NULL,0,0),(2404,2520,'description','Colony macroscopically a blackishbrown mat growing subaerially on a wet rock face, mucilaginous to the touch. Colony in laboratorygrown cultures on agar-solidified media in slants a blackish mat with a purplish-brown cast, not penetrating the agar. Filaments usually lacking a bulbous swollen base, in wider trichomes sometimes with swollen basal region, gradually tapering from the base to the apex, rarely false branched, less than 30 um long in young filaments, up to 250 um long in mature filaments. Sheath thin, firm, colorless, not lamellated, usually tightly bound to the cells of the trichome but at times becoming wider with the edge of the sheath clearly visible apart from the cellular portion of the filament, often extending beyond the distal end of the trichome (hormogonia release?), in regions where fragmentation of the trichome has occurred frequently gelatinized and forming a widened sphere or oval around the trichome ends and achieving a diameter of 8–13 um. Trichomes consistently constricted at the cross walls throughout the length of the trichome, but with constrictions sometimes obscured by the tight sheath, especially strongly constricted in basal and mid-regions regions, appearing less constricted at the terminal regions of mature filaments, in basal region near heterocyte 3.5–8.0 um wide, in intercalary region 2.5–5.5 um wide, and in terminal region 2.5–4.8 um in wide. Vegetative cells purplish in color, granular in the centroplasm, with prominent spherical polyphosphate granules, mostly shorter than wide to isodiametric, sometimes longer than wide, 2.0–11.0 um long near the base, 1.4–8.0 um long in the middle part of the trichome, becoming 3.4–6.0 um long near the terminus. Heterocytes mostly terminal, basal in position, yellow in color, spherical or with clearly rounded free terminal ends and flattened to the adjacent vegetative cell, sometimes in pairs or series, the newer cell subterminal to the older senescing heterocyte, 2.5–5.5 um long, 3.0–6.4 um wide, with intercalary heterocytes discoid, 1.6–2.8 um long, 5.8–6.0 um wide. Necridia rare. Akinetes not observed.','Kumar et al. 2022',NULL,0,0),(2405,2520,'etymology','Named for the island of Oahu, Hawai’i, from which the sample was collected.','Kumar et al. 2022',NULL,0,0),(2406,2521,'description','Filaments heteropolar, wider in the basal region, which is bulbous, gradually tapering to the distal end, but not forming a terminal hyaline hair, or isopolar and tapering toward both ends, or isopolar and untapered when present as hormogonia. Akinetes absent. Heterocytes forming in pairs in middle of isopolar filaments, leading to fragmentation of the filament and formation of heteropolar filaments, having the appearance of being basal and solitary.','Kumar et al. 2022',NULL,0,0),(2407,2521,'diagnosis','Similar in morphology to <em>Calothrix</em>, <em>Fulbrightiella</em>, <em>Dulcicalothrix</em>, <em>Macrochaete</em>, and <em>Roholtiella</em>, but distinctive in the formation of pairs of heterocytes in mid-filament in isopolar filaments, leading to fragmentation of filament to form heteropolar filaments. Also phylogenetically separate from those genera and with percent similarity of the 16S rRNA genes &lt;94.5% in comparison to other tapering genera.','Kumar et al. 2022',NULL,0,0),(2408,2521,'etymology','Named in honor of Professor Alison R. Sherwood, noted phylogeneticist, collaborator, and friend who secured NSF support for the sampling of the Hawaiian Islands that led to the discovery of this genus and species.','Kumar et al. 2022',NULL,0,0),(2409,2522,'description','Colony on agar-solidified media a dark olive-green spreading mat. Filaments isopolar and untapered, or isopolar and tapered toward both apices, or heteropolar with a basal heterocyte and tapered distal end, usually lacking a bulbous swollen base, in wider trichomes sometimes with swollen basal region, gradually tapering from the base to the apex, lacking a terminal hair, rarely false branched, less than 30 um long in hormogonia, up to 80 um long in mature filaments, heteropolar tapering filaments lacking heterocytes also form through simple fragmentation of isopolar filaments. Sheath thin, colorless, often not evident, not lamellated, usually tightly bound to the cells of the trichome when present, sometimes soft and widened, rarely extending beyond the distal end of the trichome. Trichomes constricted at the cross walls at the basal and mid-trichome regions, becoming unconstructed or only slightly constricted toward the distal ends, with constrictions sometimes obscured by the sheath, in basal region adjacent to heterocyte 6.0–8.4 um wide, in intercalary region 3.6–5.0 um wide, and in terminal region 2.0–3.0 um in wide. Vegetative cells blue-green in color, with prominent spherical polyphosphate granules present in the centroplasm, mostly shorter than wide to isodiametric, longer than wide only in the distal apical regions, 3.0–6.0 um long near the base, 2.5–4.5 um long in the middle part of the trichome, becoming 4.0–6.0 um long at the terminus. Heterocytes rare, forming in pairs in mid-filament, but having the appearance of being terminal after trichome fragmentation, sometimes senescing and forming secondary basal heterocyte adjacent to the degenerating heterocyte, yellow in color, with clearly rounded free terminal ends and flattened to the adjacent vegetative cell, solitary, 2.5–4.0 um long, 4.0–6.0 um wide. Necridia and akinetes not observed.','Kumar et al. 2022',NULL,0,0),(2410,2522,'diagnosis','Differentiated from other heterocytous tapering genera by the formation of isopolar filaments that taper toward both ends, which become heteropolar only after fragmentation mid-filament by simple fragmentation or following formation of a pair of heterocytes.','Kumar et al. 2022',NULL,0,0),(2411,2522,'etymology','Named for the island of Maui, Hawai’i, from which the sample was collected.','Kumar et al. 2022',NULL,0,0),(2412,2523,'description','Filaments generally unbranched, with a single trichome per sheath. Sheath unlamellated, colorless, firm, thin, not evident in older trichomes consisting mostly of akinetes. Trichomes constricted at the crosswalls, isopolar, with metameric heterocyte formation, with apoheterocytic akinete formation, very rarely with single false branching, (4.3)–5–6.2–(6.8) um wide in actively growing cultures, up to 8 um wide in older trichomes. Vegetative cells blue-green, granular, barrel-shaped to cylindrical, (2.3)–5.2–7.7–(11.4) um long, with median length of 6.5 mm. Intercalary heterocytes produced singly or in pairs, with two polar nodules, similar in diameter to vegetative cells, 4.8–8.6 um wide, (4.4)–7–11–(18.4) um long. Terminal heterocytes produced singly at terminus, with a single polar nodule, generally spherical or globose, (5.1)–6.4–7.7–(9.7) um wide, 4.5–9.8 um long. Akinetes produced in long series, excreting brownish wall material particularly into crosswalls, which become dark brown and thickened, 4.4–5.7 um wide, 4.3–11 mm long. Hormogonia developing from akinetes, emerging from lateral walls, growing perpendicular to main axis of trichome.','Lukešová et al. 2009',NULL,0,0),(2413,2523,'etymology','<em>Aulosira bohemensis</em> = <em>Aulosira </em>from Bohemia','Lukešová et al. 2009',NULL,0,0),(2414,2523,'diagnosis','Most similar to <em>Aulosira terrestre</em> Subba-Raju, from which it differs by shorter and wider cells and by germination of akinetes perpendicular to the trichome axis.','Lukešová et al. 2009',NULL,0,0),(2415,2530,'description','Unicellular cyanobacteria with cell diameter below 3 lm and parietal thylakoid arrangement. The members are morphologically cryptic to other cyanobacterial groups (Synechococcales, Prochlorococcales, etc.). This order is currently defined mainly by phylogenetic clustering (Figs. 1, 2, 5.6, S1).','Strunecký et al. 2023',NULL,0,0),(2416,57,'description','This family currently consists of an isolated lineage with a single genus isolated from ascidians (Miyashita et al. 2003), epiphytic on marine macroalgae (Ohkubo et al. 2006), or from the coastal marine benthos. Spheroidal or oval cells sized 1.5–2.5 lm have 7–15 continuous concentric thylakoid membranes and closely stacked phycobilisomes (Marquardt et al. 2000, Chen et al. 2009). The prominent ability of Acaryochloris to produce chlorophyll d (chl d) as the main photosynthetic pigment was believed to support its unique position among cyanobacteria (Miyashita et al. 2003). Later, it was found that phylogenetically close Acaryochloris thomasi did not produce chl d, and instead, it possesses monovinyl-chl a and chl b (Partensky et al. 2018). Simultaneously, various cyanobacteria from different orders were reported to contain chl d (Gomez-Lojero et al. 2018). Thus, the production of chl d does not seem to be a valid diacritical marker of Acaryochloridaceae.','Strunecký et al. 2023',NULL,0,0),(2417,2533,'description','Thallus fasciculated, blue-green or yellow-green when old. Cylindrical, straight or twisted trichomes, sometimes bent and coiled, not attenuated, constricted at the cross-walls with variable cell size within trichomes; with pairs of cells having conical trim outside of common cell wall, hyaline and firm sheath. End cells rounded, not calyptrate. Cells yellowishgreen to pale green, sometimes with orange granules and visible stacked thylakoids, always wider than long, (1.4) 1.8–2 (2.9) μm long, (4.7) 5–6.5 (7.1) μm wide. Apical cell not capitate, cell content without aerotopes. Hormogonia formation by characteristic thin biconcave necridic cells. (Figs 7A–G, 9A)','Strunecký et al. 2020',NULL,0,0),(2418,2533,'etymology','alaskaensis (L.): found at Alaska','Strunecký et al. 2020',NULL,0,0),(2419,2534,'description','Thallus bright green to yellow-brownwhen old with characteristic growth pattern on agar makingwell isolated spots . Trichomes solitary, not fasciculated, bright yellow-green to olive green, with characteristic 90 degrees turned cell within the trichome (Fig. 6B and G), occasionally 1–12 thin cells (hair) at the end of filament (0.8–1.3 μm wide, 1.4–3 μm long) (Fig. 6E, F and H), occasionally false branching (Fig. 6A), not constricted at cross-walls, necridia not observed. Cells mostly isodiametric, or longer than wide before division, with parietal thylakoids, 1.8–3 μm wide, 1.9–4 μm long. End cells tapered, rounded, making characteristic mushroom like calyptra. Sheath clear, thin, and firm, occasionally widened. Freshwater, periphytic on roots or in snow. (Fig. 6A–L, 9F)','Strunecký et al. 2020',NULL,0,0),(2420,2534,'etymology','<em>alaskaensis </em>(L.): found at Alaska.','Strunecký et al. 2020',NULL,0,0),(2421,2535,'description','Trichomes flexuous, irregularly curved and coiled, untapered, cylindrical, isopolar, uniseriate, not constricted at the visible cross-walls, always with thin sheath, without necridia and hormogonia. Cells 1.1–1.6 μmwide, &nbsp;isodiametric or slightly longer 1.6–3 μm than wide. End terminal cells rounded. The main diacritical feature is the arctuation of the majority of filaments but they are never spirally coiled nor false branched.','Strunecký et al. 2020',NULL,0,0),(2422,2535,'etymology','alaskaensis (L.): found at Alaska','Strunecký et al. 2020',NULL,0,0),(2423,2536,'description','Thallus entangled in mats forming an intensely green surface layer. Filaments straight, curved, flexuose orwavy, solitary, one filament per sheath. Motile. Filaments pale bluegreen to dark green, slightly constricted at cross-walls, may become slightly wider on the apical part of filament. Sheaths thick, colorless. Filaments 1–1.5 (1.6) μm wide, without necridic cells. Cell length 1.4–4.3 μm. Cells barrel-shaped longer than wide, isodiametric or shorter than wide, with central granules in cells. Uniseriate, length of cells differs at opposite trichome ends. Apical cell is rounded without calyptra. In young cultures cells are longer than wide whereas with central granules, in old cultures (∼4–6 weeks) cells isodiametric or shorter than wide.','Strunecký et al. 2020',NULL,0,0),(2424,2536,'etymology','<em>alaskaensis </em>(L.): found at Alaska.','Strunecký et al. 2020',NULL,0,0),(2425,2537,'description','Filamentous; filaments solitary, joined into microscopic mats, firm, tube-like, colorless multilayered sheaths, commonly and intensely irregularly falsely branched. Trichomes, cylindrical, isopolar, uniseriate, irregularly curved and coiled, (1.9)2.2–2.7(4) μm wide, composed of barrel-shaped cells constricted at cross-walls, not attenuated to the ends, nonmotile. Cells isodiametric or slightly shorter than wide with cell length (1)1.2–2.5(3.4) μm, without aerotopes, without necridia and hormogonia, green. End cells conically-rounded. Cell division crosswise, perpendicular to the long axis of a trichome, daughter cells grow to the original size before the next division. Isolated from soil.','Strunecký et al. 2020',NULL,0,0),(2426,2537,'etymology','<em>americanum </em>(L.): from the Americas, to date all sequenced strains were found at North or South America','Strunecký et al. 2020',NULL,0,0),(2427,2538,'description','Thallus thin, yellow-green, green or yellow-brown. Cylindrical filaments without necridic cells solitary or densely entangled to mats. Trichomes long, wavy, typically spirally coiled, rarely straight, untapered, isopolar with rounded-end cells, 0.6–1 μm wide, intensely motile. Sheets thin and firmly attached to filaments. Cells not or slightly constricted at the translucent crosswalls. Phylogenetically distinct from all other genera in the Synechococcales.','Strunecký et al. 2020',NULL,0,0),(2428,2538,'etymology','<em>Gibliniella </em>named in honor of Anne E. Giblin, a well–known North American ecologist who studies anthropogenic inputs to ecosystems','Strunecký et al. 2020',NULL,0,0),(2429,2539,'description','Thallus yellow-green to green. Trichomes solitary or fasciculated, wavy, spirally coiled, rarely straight, bright yellow-green to bright green, without false branching, not constricted at cross-walls, necridia not observed, intensely motile. Cells mostly longer than wide,with parietal thylakoids, 0.7–1μm wide. End cells rounded. Sheath clear, thin and firm. Freshwater in lake.','Strunecký et al. 2020',NULL,0,0),(2430,2540,'description','Filamentous cyanobacteria, forming greenish or reddish compact biofilms. Filaments fine, long, arctuated,waved or intensely coiled, ensheathed and unbranched without necridic cells. Sheaths colorless, thin, firm, enveloping one trichome and usually firmly attached. Trichomes fine 1–3 μm wide, cylindrical, slightly constricted at cross-walls. Up to date found in the Antarctic and north of North America.','Strunecký et al. 2020',NULL,0,0),(2431,2541,'description','Filaments short to long, curved, wavy or coiled, with colorless, thin sheaths. Filaments 1–1.5 (2) μm wide, slightly constricted on cross-walls, without necridic cells, cells longer than wide 1.7–7 (10) μm long, without aerotopes, with prominent parietal thylakoid pattern, pale blue-green, brownish, olive green, yellowish or reddish; end cells without thickened cell walls or calyptras. Cells divide by a symmetrical crosswise binary fission; cells grow long before next division. Heterocytes and akinetes absent. Apical cell rounded, long with prominent granules at the apex. Freshwater in flowing water or forming thick mats at lake bottom.','Strunecký et al. 2020',NULL,0,0),(2432,2540,'etymology','the generic name ‘Shackletoniella’ was derived from the name of Sir Ernest Shackleton, a polar explorer who led British expeditions to the Antarctic including scientific investigations','Strunecký et al. 2020',NULL,0,0),(2433,2542,'description','Macroscopic growth as gray or grayblue irregular flake-like colonies found in soil. Colonies have very loose mucilaginous texture without periderm. Filaments isopolar, straight or curved, and twisted. Filaments show presence of lightly colored sheath with 0.6–2.0 um thickness. Vegetative cells barrel-shaped, spherical to cylindrical, bluegreen to gray-green, 4.0–5.0 um long, and 2.5–3.0 um wide or 2.2–3.7 um in diameter, with granular polyphosphate inclusions. Cell wall thin or thickened and brownish. Terminal vegetative cells not differ in shape and size. Terminal heterocytes spherical, 3.0–5.7 in diameter. Intercalary heterocytes yellowish to brownish, solitary or recorded in rows, oval to cylindrical, 6.2–8.0 um long to 4.7–6.0 um wide. Akinetes large, spherical to oval or oblong, solitary or successively in row, maximally to 6 beside one another, 6.4–8.0 um long to 5.7–6.6 um wide. Akinetes gray-green, granular with thick colorless smooth сell wall. Hormogonia visible, both with and without heterocytes. Reproduction by motile hormogonia, fragmentation of filaments and thallus, and akinetes. Gas vesicles present in hormogonia.','Maltseva et al. 2022',NULL,0,0),(2434,2542,'etymology','The species epithet “vietnamicum” refers to country of isolation, Vietnam.','Maltseva et al. 2022',NULL,0,0),(2435,2543,'description','An order defined mainly by monophyletic clustering in multigene and 16S rRNA gene phylogenies (Figs. 1, 2, 5.9, S1). The majority of included strains are filamentous with cell widths below 2 um and parietal thylakoids. Strains with isodiametric cells up to twice as long before division are cryptic to Leptolyngbyaceae. The rest of the strains with cylindrical cells several times longer than wide are slightly thinner than Prochlorotrichales; however, their morphological divergence is low. Ecological distribution is highly diverse.','Strunecký et al 2023',NULL,0,0),(2436,2544,'description','Based on Nodosilinea (Perkerson et al. 2011), Nodosilineaceae, however, includes strains with diverse trichome morphologies and ecological requirements. Trichomes are usually flexuous, short or long, solitary or entangled, forming nodules, straight, bent, or spirally coiled. Reproduction by disintegration of the trichomes into motile hormogonia without production of necridic cells. Cell division in two planes was observed in Nodosilinea. Cell size probably varies according to growth conditions, and it is generally 1–3.5 um wide, 2–5 times longer than wide (5–10 um), slightly constricted at cross walls. The family exhibits strictly parietal thylakoid architecture, and polyphosphate granules may occur close to cell walls. Prominent aerotopes were found in the benthic genus Halomicronema (Abed et al. 2002).','Strunecký et al. 2023',NULL,0,0);
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INSERT INTO `cyanodb_excludenda` VALUES (1,'Achronema','Skuja, 1948. Symb. bot. upsal. 9(3): 30.','Bacteria (Thiobacteriae).',0),(2,'Actinocephalum','Saito, 1905. Bot. Mag. Tokyo 19: 36.','Fungi.',0),(3,'Algolia','Ørsted, 1844. De region. mar., p. 44.','Fungi (?)',0),(4,'Allogonium','Kützing, 1843. Phycol. gener., p. 245.','red alga (Bangiaceae).',0),(5,'Anhaltia','S. H. Schwabe, 1834. Linnaea 9: 127.','Bacteria (?).',0),(6,'Aspalatia','Ercegović, 1927. Acta Bot. Inst. Bot. Univ. Zagreb. 2: 82.','germlings of BANGIA (Bangiaceae); (FREMY 1934, GEITLER 1942).',0),(7,'Asterocystis','Gobi, 1879. Arb. St. Petersb. Ges. Naturf. 10: 83.','red alga (Bangiaceae).',0),(8,'Asterothrix','Kützing, 1843. Phycol. gener., p. 200.','Fungi (?).',0),(9,'Atractella','Printz, 1921. Kgl. Norske Vidensk. Selsk. Skr. 1920, 1: 93.','? (Oscillatoriales), unclear description.',0),(10,'Artactiella','Saccardo, 1886. Syll. Fung. 4: 578.','Fungi.',0),(11,'Beggiatoa','Trevisan, 1845. Nomencl. Alg. 58.','Bacteria (nom. cons. among bacteria, against Trevisan, 1842).',0),(12,'Boanema','Ercegović, 1927. Acta Bot. Inst. Bot. Univ. Zagreb. 2: 84.','development stage of NEMALION (Rhodophyceae)',0),(13,'Brachtia','Trevisan, 1848. Algae cocc., p. 57.','green alga (Chlorophyceae)',0),(14,'Bromicolla','Eichwald, 1843. Forh. Skand. Naturf. Mote 3: 615.','green alga (Chlorophyceae)',0),(15,'Byssus','[Mich.] Linné, 1753. Spec. plant., p. 1168.','mixture of algae, incl. APHANIZOMENON (pre-starting-point).',0),(16,'Calialoa','Trevisan, 1848. Alghe cocc., 41.','unidentifiable',0),(17,'Callonema','Reinsch, 1874-1875. Contr. Algol. Fungol., p. 40.','Rhodophyceae (?).',0),(18,'Camptothrix','West et West, 1897. J. Bot. 35: 269.','unidentifiable, probably initial stages of another cyanophyte-species.',0),(19,'Chaetococcus','Kützing, 1849. Tab. phycol. 1: 51.','unidentifiable.',0),(20,'Chalarodora','Pascher, 1929. Jahrb. wiss. Bot. 71: 460.','genus of Glaucophyceae.',0),(21,'Chamaesiphonosira','Geitler, 1975. Arch. Microbiol. 103: 234-236.','Bacteria.',0),(22,'Chlorobium','Nadson, 1906. Bull. Jard. Bot. St. Petersburg 6: 190.','Bacteria.',0),(23,'Chroodactylon','Hansgirg, 1855. Ber. Dtsch. Bot. Ges. 3: 14.','red alga (Rhodophyceae).',0),(24,'Chroostipes','Pascher, 1914. Ber. Dtsch. Bot. Ges. 32: 351.','probably bacteria.',0),(25,'Chroothece','Hansgirg, 1884. Österr. bot. Ztschr. 34: 352.','red alga (Rhodophyceae).',0),(26,'Chrysostigma','Kirchner, 1843','pre-starting-point name, probably used for Scytonema cincinatum.',0),(27,'Chthonoblastus','Kützing, 1843','pre-starting-point name, used for different genera, mainly from Oscillatoriales (unclear typification).',0),(28,'Cladiscothallus','Renault, 1896. Etud. Gites Min. France, 553.','fossil alga (Cyanophyte ?).',0),(29,'Clathrochloris','Geitler, 1925. Pascher´s Süsswasserfl. 12: 457.','Bacteria.',0),(30,'Clonothrix','Roze, 1896. J. Bot. 10: 325.','Bacteria.',0),(31,'Collenia','Walcott, 1914. Smiths. Misc. Coll. 64(2): 110.','fossil species of Cyanophytes.',0),(32,'Conidiothrix','Benecke et Petersen, 1921. Dansk Bot. Arkiv. 4(1): 8.','Bacteria.',0),(33,'Constantinea','Postels et Ruprecht, 1840. III. Alg., p. 17.','red alga (Rhodophyceae).',0),(34,'Cyanidium','Geitler, 1935. Arch. Hydrobiol., Suppl. 12: 624.','red alga (Rhodophyceae)',0),(35,'Cyanochaete','Gobi, 1916. Bot. Jap. 30: 6.','GLOEOCHAETE Lagerh., 1883; (Glaucophyceae), nomen altern.',0),(36,'Cyanocloster','Kufferath, 1929. Ann. Crypt. Exot. 2: 49.','probably MONORAPHIDIUM (Chlorellales, Chlorophyceae); type-species; C. muscicolus from Costarica.',0),(37,'Cyanococcus','Hansgirg, 1905. Beih. Bot. Centralbl. 18, 2: 521.','? (possibly Glaucophyceae).',0),(38,'Cyanocyta','Hall et Claus, 1963. J. Cell. Biol. 19: 558.','Glaucophyceae.',0),(39,'Cyanophora','Koršikov, 1924. Russ. Arch. Protistol. 3: 57, 71.','Glaucophyceae.',0),(40,'Cyanoptyche','Pascher, 1929. Jahrb. wiss. Bot. 71: 459.','Glaucophyceae.',0),(41,'Cyanotheca','Pascher, 1914. Ber. Dtsch. Bot. Ges. 32: 351.','Bacteria (Caulobacteriae); see Claus, 1961.',0),(42,'Cyclosperma','Bonnemaison, 1822. J. phys. 44: 179.','pre-starting-point syn. to LYNGBYA G. Agardh ex Gomont, 1892 (?).',0),(43,'Dactylococcopsis','Hansgirg, 1888. Notarisia 3: 590.','green algae from the genera MONORAPHIDIUM and ANKISTRODESMUS (Chlorellales, Chlorophyceae); type-species: D. rupestris from Czechoslovakia; sensu auct. post. = RHABDOGLOEA Schröder, 1917; or MYXOBAKTRON Schmidle, 1904.',0),(44,'Dactylogloea','Borzi (1887) ex Borzi, 1914. N. Giorn. Bot. Ital., N. S. 21(4): 348, 358.','1887 – nomen nudum, 1914 – unidentifiable (Oscillatoriales ?).',0),(45,'Dermocarpa','Crouan et Crouan, 1858. Ann. Sci. Nat. Bot., ser. 4, 9: 70.','nomen ambiguum (type = mixture of different species from different genera); see Komárek et Anagnostidis, 1986.',0),(46,'Dermogloea','Zanardini, 1872. Atti R. Istr. Veneto Sci. Lett. Arti, ser. 4, 1: 1885.','undefiniable.',0),(47,'Desmanthos','Skuja, 1956. Nova Acta Reg. Soc. Sci. Upsal., ser. 4, 16(3): 83.','Bacteria; later homonym to DESMANTHUS Willdenow 1806 nom. cons.; = SKUJAEPHYCONEMA Burkart, 1959.',0),(48,'Detoniella','Trevisan in De Toni et Trevisan, 1889. Syll. Schizomyc., p. 929.','Bacteria.',0),(49,'Elisa','Gray, 1821. New Arr. Brit. Pl. 1: 282.','mixture of filamentous Cyanophytes and Algae.',0),(50,'Embryosphaera','Trevisan, 1848. Alg. coccot., p. 36.','green alga (Chlorophyceae).',0),(51,'Entothrix','Kützing, 1843. Phycol gener., p. 224.','unidentifiable; ex Forti 1907 = probably MICROCOLEUS.',0),(52,'Ernstiella','Chodat, 1911. Bull. Soc. Bot. Genéve 2, ser. 3: 125.','mixture of Cyanophyte species (from the genera SIPHONONEMA, CHAMAESIPHON,',0),(53,'Erythroconis','Orsted, 1842. Naturhist. Tidsskr. 3: 555.','unidentifiable.',0),(54,'Euactis','Kützing, 1843. Phycol. gener., p. 240.','pre-starting-point name, unclear taxonomic position; probably RIVULARIA.',0),(55,'Exococcus','Nägeli, 1847. Neue Denkschr. Allg. Schweiz. Ges. Gesammten Naturwiss. 9(2): 170.','unidentifiable genus and species from Cyanophyceae (? Hydrococcaceae).',0),(56,'Filarszkia','Forti in De Toni, 1907. Syll. Alg. 5: 258.','hormocysts of Scytonema (?).',0),(57,'Fridaea','Wille, 1909. In Engler & Prantl, Nat. Pflanzenfam., Nachtr. 1(2): 77, 79.','later homonym (orth. var.) to FRIEDAEA Schmidle, 1905; (Chlorophyceae).',0),(58,'Gervasia','Borzi ex Forti in De-Toni, 1907. Syll. Alg. 5: 704.','nomen nudum.',0),(59,'Girardia','Gray, 1821. New Arr. Brit. Pl., 1: 287.','unidentifiable.',0),(60,'Glaucocystis','Itzigsohn in Rabenhorst, 1854. Alg. eur. Exsicc., n. 1935.','Glaucophyceae.',0),(61,'Glaucocystopsis','Bourrelly, 1960. C. R. Hebd. Séances Acad. Sci. 251: 416.','Glaucophyceae.',0),(62,'Glaucosphaera','Koršikov, 1930. Arch. Protistenk. 70: 222.','Glaucophyceae.',0),(63,'Goliothrix','Zopf, 1882. Morph. Spaltpfl., p. 51.','mixture of different Cyanophytes.',0),(64,'Gloeochaete','Lagerheim, 1883. Öfvers. Kgl. Vetensk. – Ak. Förhandl. 1883, 2: 39.','Glaucophyceae.',0),(65,'Gloeocapsomorpha','Zalesskij, 1918. Ežeg. Russk. Paleontol. Obšč. 1: 34.','fossil cyanophyte genus.',0),(66,'Gloionema','Agardh, 1817. Syn. Alg. Scand., p. 120.','pre-starting-point syn. of MICROCOLEUS (?).',0),(67,'Goniotrichum','Kützing, 1843. Linnaea 17: 89.','red alga (Bangiaceae, Rhodophyceae).',0),(68,'Guyotia','Schmidle, 1905. Allg. Bot. Ztschr. 11: 64.','unclear described, unidentifiable genus (PLACOMA ?).',0),(69,'Hapalopsis','Kufferath, 1942. Bull. Soc. Roy. Bot. Belg. 74: 96.','stage of  STIGONEMA (?).',0),(70,'Haplonema','Borzi, 1914.','probably invalidly published, taxonomically unclear.',0),(71,'Hassallia','Trevisan, 1848. Alghe cocc., p. 67.','later (and pre-starting-point) homonym to HASSALLIA Berkeley, 1845 (= HASSALLIA',0),(72,'Havrella','Breton et Saulot, 1986. Cryptogamie – Algologie 7, 4: 286-287.','Bacteria.',0),(73,'Heterochroa','Areschoug, 1866. Alg. Scand. Exs., ser. 2, 6: 289.','later homonym to HETEROCHROA Bunge in Ledebour, 1830; pre-starting-point syn., probably to SCHIZOTHRIX Kützing ex Gomont, 1892 (?).',0),(74,'Homalococcus','Kützing, 1863. Osterpr. Realschule Nordhausen, p. 6.','unidentifiable.',0),(75,'Hormobolus','Borzi, 1914. Boll. Stud. Inform. Reale Giard. Colon. 1: 93.','probably SCYTONEMA Agardh ex Bornet et Flahault, 1886 (?).',0),(76,'Humida','Gray, 1821. New Arr. Brit. Pl. 1: 281.','unidentifiable, mixture of filamentous Cyanophytes.',0),(77,'Hygrocrocis','C. A. Agardh, 1824. Syst. Alg. 23: 45.','Bacteria.',0),(78,'Ialomitzia','Gruia, 1969. Rev. Algol., ser. 2, 7: 292.','unclearly described, not revised (probably Fungi imperf.; comp. BOURRELLY 1970).',0),(79,'Juguspira','Crow, 1927. Trans. Amer. Micr. Soc. 46: 147.','unclearly described, confused morphology.',0),(80,'Kirchneriellopsis','Kufferath in Conrad et Kufferath, 1954. Mém. Inst. Roy. Sci. Nat. Belg. 127: 271.','probably coccal green alga without pyrenoid (? syn. with RAPHIDOCELIS).',0),(81,'Kneuckeria','Schmidle, 1905. Allg. Bot. Ztschr. 1905: 64.','red alga (Bangiaceae, Rhodophyceae).',0),(82,'Krkia','Pevalek, 1929. Acta Bot. Inst. Bot. Univ. Zagreb 6: 16.','unclearly described, probably syn. with CYANOCYSTIS (?).',0),(83,'Kyanostichus','Romanov, 1964. Two new algae from a Calif. Oxid. Pond, p. 1.','indeterminable cyanophyte species (?).',0),(84,'Kybotion','Pascher, 1940. Arch. Protistenk. 93: 348.','Chrysophyceae.',0),(85,'Lagerheimiella','Borzi, 1914.','non ”LAGERHEIMIELLA Boedijn, 1940”; probably invalidly published, unclear.',0),(86,'Lampropedia','Schroeter, 1886. In Cohn, Kryptogamenfl. Schlesiens, 1: 151.','Bacteria; later homonym is LAMPROPEDIA Pringsheim, 1966.',0),(87,'Leptothrix','Kützing, 1843. Phycol. gener., p. 198.','Bacteria.',0),(88,'Leuconostoc','Van Tieghem, 1878. Ann. Sci. Nat. Bot. 7(6): 198.','Bacteria.',0),(89,'Leucothrix','Örsted, 1844. De region mar., p. 44.','Bacteria.',0),(90,'Limnactis','Kützing, 1843. Phycol. gener., p. 237.','mixture of GLOEOTRICHIA and RIVULARIA, pre-starting-point genus.',0),(91,'Lithonema','Hassall, 1845.','pre-starting-point name, unclear; not LITHONEMA Ercegović, 1929.',0),(92,'Lophopodium','Kützing, 1849. Tab. Phycol. 1: 45.','unclear filamentous, heteropolar genus of Cyanophytes.',0),(93,'Loten','Adanson, 1763. Fam. Plant. 2: 3.','mixture of filamentous Cyanophytes.',0),(94,'Marssoniella','Lemmermann, 1900. Ber. Dtsch. Bot. Ges. 18: 275.','spores of GURLEYA (Microsporidia); see Komárek & Vávra, 1968.',0),(95,'Mastichothrix','Kützing, 1843.','pre-starting-point name, unclear content.',0),(96,'Mastigothrix','Reinsch, 1867.','pre-starting-point name, unclear; not MASTIGOTHRIX Poche, 1913.',0),(97,'Merismoarcus','Hindák, 1988. Biológia, Bratislava, 43: 749.','probably Bacteria.',0),(98,'Merizomyria','Pollini, 1817. Biblkioth. Ital. 7: 420.','unclear, probably a mixture of filamentous Cyanophytes; STIGONEMA (?).',0),(99,'Micraloa','Biasoletto, 1832. Alg. microsc., p. 44-47.','unclear, according to Drouet & Daily, 1956 = fytoflagellates; type species: M. protogenita.',0),(100,'Micrascidium','Borzi, 1914.','unclear, probably never validly published.',0),(101,'Microcystis','Kützing, 1833. Linnaea 8: 372.','green algae (Chlorophyceae).',0),(102,'Microdiscus','Steinecke, 1915. Schr. Phys.-ökon. Ges. Königsberg 56: 25.','unclear, epiphytic on CLOSTERIUM; type species = M. parasiticus (unclear reproduction, not revised).',0),(103,'Microhaloa','Kützing, 1843. Phycol. gener., p. 169.','mixture of coccal Cyanophytes and green algae.',0),(104,'Montanoa','Guerrero, 1947. Anal. Jard. Bot. Madrid 7: 267.','unclear description, possibly CALOTHRIX (?).',0),(105,'Nelliecarteria','De-Toni, 1936. Nomencl. Algol. 8: 5.','Fungi.',0),(106,'Nemacola','Massalongo, 1955. Flora 38: 36.','unclear, probably a pre-starting-point syn. to MICROCOLEUS (?).',0),(107,'Nematococcus','Kützing, 1833. Linnaea 8: 381.','Fungi.',0),(108,'Neoadelia','Bompard, 1867. Hedwigia 6: 129.','unclear, probably pre-starting-point syn. to SYMPLOCA Kützing ex Gomont, 1892.',0),(109,'Oligoclonium','Brooker-Klugh, 1921. Contr. Canad. Biol. 1918/20: 181.','degenerated oscillatoriacean trichomes.',0),(110,'Oscillaria','sensu auct.','pre-starting-point orth. var. of OSCILLATORIA Vaucher ex Gomont, 1892.',0),(111,'Palmogloea','Kützing, 1843. Phycol. gener., p. 176.','mixture of green algae with (?) APHANOCAPSA.',0),(112,'Paraplectonema','Frémy, 1939. Arch. Bot. 3: 178.','Bacteria.',0),(113,'Paulinella','Lauterborn, 1895. Ztschr. Wiss. Zool., p. 59.','syncyanotic genus of Testacea with cyanelles.',0),(114,'Pediochloris','Geitler, 1925. In Pascher´s Süsswasserfl. 12: 457.','Bacteria.',0),(115,'Pelodictyon','Lauterborn, 1913. Allg. Bot. Ztschr. 19: 98.','Bacteria.',0),(116,'Pelonema','Lauterborn, 1916. Verh. Naturh. Med. Ver. Heidelberg 13: 408.','Bacteria.',0),(117,'Peloploca','Lauterborn, 1913. Allg. Bot. Zrschr. 19: 99.','Bacteria.',0),(118,'Phragmonema','Zopf, 1882. Morph. Spaltpfl., p. 49.','red alga (Rhodophyceae).',0),(119,'Phytoconis','Bory de Saint Vincent, 1797. Mém. Conferva & Byssus, p. 52.','unidentifiable.',0),(120,'Pilgeria','Schmidle, 1901. Hedwigia 40: 53.','unclear, unidentifiable.',0),(121,'Pleococcus','Kützing, 1843. Linnaea 17: 84.','syn. of ”BOTRYDINA Brébisson” (= consortium of COCCOMYXA with protonemes).',0),(122,'Pleurococcus','Meneghini, 1837. Consp. Algol. Eugan., 337.','nomen ambiguum, type = probably green alga (Chlorophyceae).',0),(123,'Pluto','Copeland, 1936. Ann. N. Y. Acad. Sci. 36: 72.','CYANIDIUM (Rhodophyceae).',0),(124,'Polycoccus','Kützing, 1843. Linnaea 17: 84.','probably developmental stage of Nostoc punctiforme.',0),(125,'Pontothrix','Nadson et Krasilnikov, 1932. Dokl. Akad. Nauk SSSR 1932 A: 264, 247.','Bacteria.',0),(126,'Porphyridium','Nägeli, 1849. Gatt. einzell. Algen, p. 71.','red alga (Bangiaceae, Rhodophyceae).',0),(127,'Portacus','Rafinesque, 1819. J. Phys. 89: 107.','unidentifiable genus, probably from Nostocales.',0),(128,'Pseudospirulina','Pankow et Jahnke, 1964. Österr. Bot. Ztschr. 111(4): 335.','stalks of Vorticella.',0),(129,'Rhizonema','Thwaites in Smith et Sowerby, 1849. Suppl. Engl. Bot. 4: 2954.','? SCYTONEMA mixed with fungal hyphae.',0),(130,'Rosaria','N. Carter, 1922. J. Linn. Soc. 16: 54.','NELLIECARTERIA (Fungi).',0),(131,'Schmidlea','Lauterborn, 1913. Allg. Bot. Zrschr. 19: 98.','Bacteria.',0),(132,'Scythymenia','Agardh, 1824. Syst. Alg., p. 20(xx).','pre-starting-point syn. of STIGONEMA Agardh ex Bornet et Flahault, 1886 (?).',0),(133,'Skujaephyconema','Burkhart, 1959. Darwiniana 11: 765.','Bacteria.',0),(134,'Skujapelta','Hall et Claus, 1967. J. Phycol. 3: 50.','Glaucophyceae.',0),(135,'Sorospora','Hassall, 1845. Brit. Freshw. Algae 1: 309.','probably mixture of several epilithic Cyanophyte species.',0),(136,'Sphaenocystis','Reinsch','erroneous citation, correctly see under ”SPHAENOSIPHON Reinsch”.',0),(137,'Sphaerothrombium','Kützing, 1833. Linnaea 8: 370.','pro syn., unclear (? MICROCYSTIS Kützing ex Lemmermann, 1907).',0),(138,'Staurocladia','González-Guerrero, 1966. A. Inst. Bot. Cavanilles 23: 135.','indeterminable Cyanophytes (?).',0),(139,'Symphyosiphon','Kützing, 1843. Phycol. gener., p. 218.','mixture of filamentous Cyanophytes.',0),(140,'Tetrapedia','Reinsch, 1867. Algenfl. Franken, p. 37.','green algae from different genera; see Geitler 1942, Claus 1963.',0),(141,'Tetrarcus','Skuja, 1934. Acta Horti Bot. Univ. Latv. 7: 46.','probably Rhodobacteria.',0),(142,'Thamniastrum','Reinsch, 1888. Notarisia 3(11): 513.','free stalk-system of  Gomphosphaeriaceae (probably of SNOWELLA).',0),(143,'Thionema','Kolkwitz, 1938. Ber. Dtsch. Bot. Ges. 56: 15.','Bacteria.',0),(144,'Thioploca','Lauterborn, 1907. Ber. Dtsch. Bot. Ges. 25: 242.','Bacteria.',0),(145,'Thiosiphon','Klas, 1936. Akad. Wiss. Wien Sitzungsb. mat.-nat. Kl., Abt. 145:213.','Bacteria.',0),(146,'Thiospirillopsis','Uphof, 1927. Arch. Hydrobiol. 18: 83.','Bacteria.',0),(147,'Thiothrix','Vinogradskij, 1888. Beitr. Morphol. Physiol. Bacter., p. 29.','Bacteria.',0),(148,'Trichocystis','Kützing, 1846. Tab. phycol. 1: 20.','? zoochlorellas.',0),(149,'Trichospira','McNeill, 1948. Castanea 13: 44.','unclear genus from Oscillatoriales; later homonym to TRICHOSPIRA Humboldt, Bonpland et Kunth, 1818.',0),(150,'Urococcus','(Hassall) Hassall et Kützing, 1849. Spec. Alg., p. 206.','green alga (Chlorophyceae).',0),(151,'Vaginaria','Bonnemaison, 1822. J. Phys., Chém., Hist. Nat. & Arts 94: 175.','pre-starting-point syn., probably to MICROCOLEUS Desmaziéres ex Gomont, 1892; later homonym to VAGINARIA Persoon, 1805.',0),(152,'Vaginaria','Gray ex Kuntze, 1898. Rev. Gen. Pl. 3(3): 435.','pre-starting-point syn., to MICROCOLEUS Desmaziéres ex Gomont, 1892; later homonym to VAGINARIA Persoon, 1805.',0),(153,'Xanthotrichum','Wille ex Schütt, 1893. Pflanzenleben Hochsee, p. 39. Cyanophyceae, Oscillatoriales, Phormidiaceae, Phormidioideae','TRICHODESMIUM Ehrenberg ex Gomont, 1892, nom. cons.',0),(154,'Zachariasia','Lemmermann, 1895. Vorarb. Fl. Plöner Seengeb., p. 60.','unclear description, not revised (with “chlorophora stellata”), probablya red alga (Bangiaceae, Rhodophyceae).',0),(155,'_Giraffa camelopardalis','Linnaeus, 1758','Originally <em>Cervus camelopardalis </em><sup>Linnaeus, 1758</sup> is nowadays considered neither a member of the genus CERVUS (=deer) nor a cyanobacterium',1),(156,'Phormidium murrayi','&nbsp;(W. et G.S.West) Anagnostidis et Komárek, 1988, &nbsp;Algological Studies 50–53: 408','',1),(157,'Moorea','Engene, Rottacker, Kaštovský, Byrum, Choi, Ellisman, Komárek et Gerwick &nbsp;2012. International Journal of Systematic and Evolutionary Microbiology &nbsp;62: 1176','name used previously in botanical literature',0),(158,'','','',0);
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INSERT INTO `cyanodb_gps` VALUES (1,'19°57′54″S','42°64′44″W','',386,0),(2,'11°11′111″N','222°22′222″E','Bratyiszlávos',374,0),(3,'11°11′12″N','222°22′21″E','Budínská Pešča',374,0),(5,'37°42′021″N','088°40′030″W','',390,0),(6,'55°57′047″N','058°15′053″E','',391,0),(7,'55°57′047″N','058°15′052″E','',392,0),(8,'34°02′029″N','116°08′042″W','',393,0),(9,'23°10′000″S','049°09′000″W','State &nbsp;Park &nbsp;of &nbsp;Santa &nbsp;Virginia',448,0),(10,'23°53′050″S','046°12′031″W','mangrove forest at the Bertioga resort, north of the municipality of Guarujá',450,0),(11,'23°20′036″S','045°04′022″W','anta Virgínia nucleus of the Serra do Mar state park, north of the municipality of Ubatuba',451,0),(12,'','','St. Croix',457,0),(13,'45°20′006″N','011°46′056″E','Garden Hotel, Euganean Thermal District, Montegrotto Terme, Padova, Italy',460,0),(14,'00°15′035″S','035°05′020″E','Lake Nakuru',461,0),(15,'48°58′000″N','014°56′000″E','',462,0),(16,'30°29′018″N','115°18′001″E','Xishui county, Hubei Province, China',464,0),(17,'25°15′036″S','045°07′040″W','',467,0),(18,'62°09′047″S','058°27′046″W','Admiralty Bay, King George Island and South Shetlands Archipelago, Antarctica',468,0),(19,'06°47′001″S','105°30′009″E','Java, near the Tamanjaya village, Ujung Kulon NP',469,0),(20,'48°28′018″N','020°29′044″E','Baradla Cave',112,0),(21,'11°28′020″N','107°20′028″E','&nbsp;Lake Hồ Đâu Co, province Đồng Nai',470,0),(22,'13°00′049″N','100°03′035″E','solar saltern in Ban Laem district, Petchaburi province',473,0),(23,'22°13′013″N','159°34′046″W','Waikapala e Cave, Kauai, Hawaii',475,0),(24,'22°12′011″N','159°33′056″W','Maniniholo Cave, Kauai, Hawaii',477,0),(25,'41°53′034″N','012°29′038″E','Domus Aurea, Rome',479,0),(26,'35°52′051″N','014°23′052″E','&nbsp;St Paul’s Catacombs, Rabat',479,0),(27,'22°12′011″N','159°33′056″W','near Maniniholo cave, Kauai, Hawaii',480,0),(28,'22°13′013″N','159°34′046″W','Waikapala &nbsp;e Cave, Kauai, Hawaii',482,0),(29,'36°38′019″N','022°22′043″E','Vlychada Cave',485,0),(30,'26°28′000″N','074°36′000″E','Thar Desert, Rajasthan, India',487,0),(31,'','','Jiaxing, Zhejiang Province, China',488,0),(32,'','','Wind flat, Zingst, Baltic Sea, Germany',490,0),(33,'','','vicinity of Wanang, Papua-New Guinea',491,0),(34,'','','Wisconsin, USA',492,0),(35,'37°01′008″N','008°55′036″W','Martinhal beach, Portugal',494,0),(36,'41°50′059″N','008°52′000″W','Moledo do Minho beach, Portugal',495,0),(37,'45°15′038″N','010°56′056″E','Lake Tovel, Italy',496,0),(38,'42°53′020″S','171°32′008″E','Mt Philistine, Arthur’s Pass National Park, New Zealand',500,0),(39,'','','Coast of Republic of Palau',426,0),(40,'','','Mt Philistine, Arthur’s Pass National Park, New Zealand',503,0),(41,'','','Mt Philistine, Arthur’s Pass National Park, New Zealand',504,0),(42,'','','Mt Philistine, Arthur’s Pass National Park, New Zealand',505,0),(43,'','','Mt Philistine, Arthur’s Pass National Park, New Zealand',506,0),(44,'','','Yellowstone - Firehole Lake',507,0),(45,'','','Roraima, Venezuela',508,0),(46,'','','Mount Roraima, Venezuela',509,0),(47,'','','Roraima mountain, Venezuela',510,0),(48,'','','Yellowstone, Firehole Lake',511,0),(49,'','','Roraima mountain, Venezuela',512,0),(50,'','','Huautla, Morelos, Mexico',513,0),(51,'','','La Media Luna, San Luis Potosí, Mexico',514,0),(52,'30°03′031″N','081°42′052″W','Pond at Fiddlers Ridge Drive, Jacksonville, FL',516,0),(53,'','','Bald Mountain, Colorado, USA',517,0),(54,'11°26′045″N','107°23′011″E','Cat Tien National Park, province Đồng Nai, Vietnam',519,0),(55,'27°13′018″S','070°20′043″W','Atacama desert, Chile',520,0),(56,'09°17′025″N','082°11′023″W','Bocas del Toro National marine park, Panama',523,0),(57,'23°35′024″N','081°31′006″W','&nbsp;Looe Key, Florida, USA',524,0),(58,'12°12′014″N','068°58′054″W','Curacao, Netherlands Antilles',525,0),(59,'27°45′019″N','080°31′019″W','Indian River Lagoon, Florida, USA',526,0),(60,'24°33′029″N','080°22′045″W','Big Pine Ledge, Florida Keys, Florida, USA',527,0),(61,'','','Curacao, Netherlands Antilles',529,0),(62,'','','New Ireland, Papua New Guinea',530,0),(63,'','','Hansa Bay, Madang Province, Papua New Guinea',530,0),(64,'','','Abaliget cave, Hungary',531,0),(65,'','','Abaliget cave, Hungary',532,0),(66,'','','Abaliget cave, Hungary',533,0),(67,'','','Abaliget cave, Hungary',534,0),(68,'','','Abaliget cave, Hungary',535,0),(69,'','','Wind flat, Zingst, Baltic Sea, Germany',498,0),(70,'','','Abaliget cave, Hungary',536,0),(71,'42°36′048″N','070°48′041″W','Chebacco Pond, Essex, Massachusetts, USA',537,0),(72,'42°36′048″N','070°38′041″W','Chebacco Pond, Essex, Massachusetts, USA',538,0),(73,'22°70′000″N','114°16′000″E','South China Sea',566,0),(74,'','','Vieste (Foggia), Italy',568,0),(75,'34°12′043″N','106°45′028″W','Sevilleta Long Term Ecological Research site, Socorro County, New Mexico, USA',571,0),(76,'20°51′030″N','100°55′041″W','&nbsp;San Miguel de Allende, Guanajuato, Mexico',572,0),(77,'25°46′009″N','171°43′059″W','Laysan island',574,0),(78,'25°46′900″N','171°43′059″W','island of Laysan',575,0),(79,'27°05′048″N','080°06′030″W','East Florida, USA',576,0),(80,'','','Eilat, Israel',384,0),(81,'34°06′035″N','115°28′049″W','Cadiz Valley, Joshua Tree National Park, San Bernadino County, California, USA',577,0),(82,'20°51′039″S','049°36′054″W','Barra Funda stream, municipality of Neves Paulista, Sao Paulo State, Brazil',579,0),(83,'20°51′039″S','049°36′054″W','Barra Funda stream, municipality of Neves Paulista, Sao Paulo State, Brazil',581,0),(84,'29°73′041″S','052°41′039″W','municipality of Cachoeira do Sul, Rio Grande do Sul State, Brazil',582,0),(85,'00°18′023″N','036°04′043″E','Lake Bogoria National Reserve, Kenya',583,0),(86,'18°59′039″S','015°52′005″E','Okandeka Spring, Etosha National Park, Namibia',584,0),(87,'','','lake Magadi, Kenya',585,0),(88,'','','lake Magadi, Kenya',586,0),(89,'19°24′054″N','155°16′030″W','Kīlauea Caldera, Hawai\'i, USA',587,0),(90,'28°58′054″N','064°24′030″W','Sargasso Sea',590,0),(91,'43°12′009″N','006°52′000″E','Mediterranean Sea',590,0),(92,'25°04′012″S','475°50′027″W','State Park of Ilha do Cardoso, State of São Paulo, Brazil',592,0),(93,'23°48′000″N','080°12′000″E','Sihora town, district Jabalpur, Madhya Pradesh, India',594,0),(94,'12°49′047″S','038°13′036″W','Jauá Beach, Camaçari city, Bahia State, Brazil',596,0),(95,'12°23′056″S','037°53′011″W','Porto Sauípe Beach, Entre Rios city, Bahia State, Brazil',596,0),(96,'13°52′055″S','038°56′032″W','Três Coqueiros -Barra Grande Beach, Cairú city, Bahia State, Brazil',597,0),(97,'23°10′054″S','044°11′012″W','Ilha Grande – Saco de Dois Rios Estuary, Angra dos Reis city, Rio de Janeiro State, Brazil',598,0),(98,'23°01′058″S','043°28′051″W','Pontal’s Beach, Rio de Janeiro city, Rio de Janeiro State, Brazil',599,0),(99,'25°33′044″S','048°19′009″W','Pontinha’s Beach, Paranaguá city, Ilha do Mel, Paraná State, Brazil',600,0),(100,'12°23′056″S','037°53′011″W','Porto Sauípe Beach, Entre Rios city, Bahia State, Brazil',601,0),(101,'03°14′034″S','060°00′029″W','Solimões River, Amazonas State, Brazil',602,0),(102,'36°39′000″N','051°24′000″E','Mazandaran province, Iran',604,0),(103,'36°44′000″N','050°50′000″E','Mazandaran province, Iran',605,0),(104,'49°25′043″N','019°29′048″E','Peat bog Klin near Námestovo, Slovakia',606,0),(105,'44°05′026″N','110°46′032″W','near La Duke Hot Spring, Montana, USA',609,0),(106,'23°32′038″N','113°23′002″E','Guangdong Province, China',610,0),(107,'','','Hoamy Reservoir, Hue area, Vietnam',612,0),(108,'19°24′058″N','097°24′013″W','Lake Alchichica, Mexico',614,0),(109,'67°03′203″N','033°30′014″E','&nbsp; &nbsp; vicinity of the Apatity town, Apatity District, Murmansk province, Kola Peninsula, Russia',616,0),(110,'37°29′006″N','112°03′047″W','Sheep Creek Drainage, in the Carmel Formation, Grand Staircase-Escalante National Monument, Utah, USA,',617,0),(111,'','','Ulu Peninsula, Antarctica',619,0),(112,'','','Baranowski glacier, Antarctica',621,0),(113,'','','Ulu Peninsula, Antarctica',624,0),(114,'','','Ulu Peninsula, Antarctica',625,0),(115,'','','Ulu Peninsula, Antarctica',626,0),(116,'','','Eilat, Israel',627,0),(117,'','','Cataloochie Road, Great Smoky Mountains National Park, Haywood County, North Carolina, USA',628,0),(118,'','','Cataloochie Road, Great Smoky Mountains National Park, Haywood County, North Carolina, USA',521,0),(119,'45°42′036″N','013°45′052″E','The Giant Cave, Sgonico, Trieste, North-Eastern Italy',631,0),(120,'45°42′036″N','013°45′052″E','The Giant Cave, Sgonico, Trieste, North-Eastern Italy',632,0),(121,'43°38′013″N','019°55′025″E','',633,0),(122,'12°12′120″N','015°25′055″E','jkkjhkjlhkljhklhlkjhkjhlkhl',658,0),(123,'5°5′250″N','12°12′36″E','ZxZXZXZX',658,0),(124,'6°6′250″S','12°13′045″W','',658,0),(125,'30°17′020″N','081°24′025″W','H. Warren Smith Cemetery, Jacksonville Beach, Florida, USA',661,0),(126,'30°17′020″N','081°24′025″W','&nbsp;Granite tombstones from the H. Warren Smith Cemetery, Jacksonville Beach, Florida,USA',662,0),(127,'39°06′066″N','110°44′713″W','',768,0),(128,'37°56′45,84″N','23°49′43,46″E','',770,0),(129,'41°17′100″N','001°54′495″E','',769,0),(130,'20°17′850″S','046°22′017″W','',777,0),(131,'25°07′059″S','047°58′019″W','',782,0),(132,'22°45′019″S','045°35′025″W','',788,0),(133,'25°07′059″S','047°58′019″W','',789,0),(134,'20°17′085″S','046°22′017″W','',790,0),(135,'23°32′038″N','113°23′002″E','',894,0),(136,'50°13′060″N','012°53′086″E','',920,0),(137,'37°19′127″N','111°31′505″W','',1036,0),(138,'37°19′127″N','111°31′505″W','',1037,0),(139,'37°49′447″N','111°25′125″W','',1038,0),(140,'37°49′447″N','111°25′125″W','',1039,0),(141,'37°49′447″N','111°25′125″W','',1044,0),(142,'37°43′012″N','111°28′273″W','',1046,0),(143,'37°49′447″N','111°25′125″W','',1047,0),(144,'37°32′35″N','111°38′26″W','',1057,0),(145,'20°1′60″N','98°54′57″W','',1062,0),(146,'19°20′006″N','097°26′045″W','',1063,0),(147,'35°36′041″N','083°46′011″W','Great Smoky Mountains NP, a cave near Cades Cove and White Oak Sink',1067,0),(148,'24°35′04″N','813°10′10″W','',1087,0),(149,'18°5′79″S','56°37′92″W','',1090,0),(150,'30°0′39″S','51°10′94″W','',1091,0),(151,'30°81′505″N','818°30′051″W','',1093,0),(152,'47°51′010″N','015°02′024″E','Lunzer See (origin of an epitype)',1101,0),(153,'15°41′174″N','961°41′528″W','',1106,0),(154,'15°41′174″N','961°41′528″W','',1115,0),(155,'18°24′042″N','109°59′006″E','Xincun Bay, Lingshui County, Hainan Province',1126,0),(156,'22°00′010″N','118°59′052″E','northern South China Sea',1128,0),(157,'26°06′059″S','152°17′023″E','',1134,0),(158,'20°51′039″S','049°36′054″W','',1135,0),(159,'12°57′006″S','038°20′042″W','',1139,0),(160,'12°44′027″S','038°09′000″W','',1140,0),(161,'03°12′047″S','058°32′041″W','Amazon',1142,0),(162,'03°16′004″S','060°00′039″W','Solimões',1142,0),(163,'30°17′020″N','081°24′026″W','',1143,0),(164,'30°17′020″N','081°24′026″W','',1144,0),(165,'','','Magny-en-Vexin',1145,0),(166,'25°25′010″N','080°39′018″W','Grass &nbsp;Prairie &nbsp;in &nbsp;Everglades &nbsp;National &nbsp;Park',1153,0),(167,'23°53′050″S','042°12′031″W','',1155,0),(168,'23°53′050″S','046°12′031″W','',1157,0),(169,'15°41′017″N','096°14′015″W','',1158,0),(170,'15°46′025″N','096°05′028″W','',1159,0),(171,'','','Nam Ngum Reservoir',1166,0),(172,'36°86′053″N','050°60′023″E','Abe siah, Ramsar, Iran.',1167,0),(173,'30°89′090″N','050°67′049″E','Talesh Mahalleh, Ramsar, Iran',1168,0),(174,'36°89′030″N','050°67′047″E','Khak sefid, Ramsar, Iran',1169,0),(175,'34°00′033″N','050°33′006″E','Hakim, Mahallat city',1171,0),(176,'34°00′041″N','050°32′046″E','Mahallat',1176,0),(177,'36°53′042″N','050°41′030″E','Saddat Mahalleh, Ramsar, Iran',1178,0),(178,'36°89′090″N','050°67′049″E','Talesh Mahalleh, Ramsar, Iran',1180,0),(179,'32°59′00″N','78°24′37″E','',1184,0),(180,'21°38′049″N','088°20′026″E','Lothian island',1187,0),(181,'23°36′000″S','045°26′000″W','',1185,0),(182,'48°56′011″N','020°21′052″E','Slovenský raj NP',1189,0),(183,'21°36′011″N','157°57′022″W','Laie Falls, Oahu, Hawaii',1191,0),(184,'','','Coimbra, Portugal',1192,0),(185,'22°42′059″S','145°25′040″E','',1193,0),(186,'18°07′008″S','143°57′040″E','Queensland: Talaroo thermal springs',1210,0),(187,'21°21′005″N','157°46′008″W','Maunawili stream, Ohahu, Hawaii',1211,0),(188,'15°41′017″N','096°14′015″W','San Agustín Bay, Huatulco, Oaxaca',1224,0),(189,'','','Near city of Most',1041,0),(190,'23°33′002″N','088°20′006″E','',1225,0),(191,'37°58′042″N','127°40′016″E','Lake Chuncheon',1226,0),(192,'37°42′031″N','127°27′007″E','Lake Cheongpyeong',1226,0),(193,'35°52′050″N','014°23′049″E','St Agatha’s Crypt in St Agatha’s Catacomb Complex, Rabat, Malta',1031,0),(194,'08°06′015″S','036°13′023″W','Tabocas reservoir near Caruaru, Pernambuco',1230,0),(195,'49°17′057″N','017°43′028″E','Bezedník pond',1247,0),(196,'20°47′004″S','049°21′033″W','',1249,0),(197,'22°40′038″S','045°38′054″W','',1250,0),(198,'23°13′003″S','044°43′011″W','',1251,0),(199,'20°47′007″S','049°21′037″W','',1252,0),(200,'30°03′030″S','051°10′017″W','',1253,0),(201,'20°21′000″S','046°38′000″W','Casca d’Anta waterfall, Serra da Canastra National Park, Minas Gerais State',1254,0),(202,'','','South Hutchinson Island, IRL, Florida',1288,0),(203,'','','Carrie Bow Cay, Belize',1289,0),(204,'45°43′085″N','035°85′025″E','',1290,0),(205,'45°47′004″N','035°85′047″E','',1291,0),(206,'57°07′018″N','014°34′022″E','',1303,0),(207,'','','Czech Republic',1304,0),(208,'','','Congo DR',1306,0),(209,'','','USA, Alaska',1311,0),(210,'','','Antarctica',1315,0),(211,'35°38′030″N','083°03′040″W','USA',1316,0),(212,'','','Latvia',1319,0),(213,'','','Amoy Island, Fukien Province, China',1323,0),(214,'','','Bijah Spring Group, Yellowstone Nat. Park, USA',1325,0),(215,'','','Antarctic',1327,0),(216,'','','Antarctic',1328,0),(217,'','','Jardin Peak near Admiralty Bay, King George Island, Antarctic',1329,0),(218,'','','James Ross Island, Antarctic',1330,0),(219,'','','USA',1333,0),(220,'','','USA',1341,1),(221,'','','USA',1345,0),(222,'','','Czech Republic',1347,0),(223,'','','France',1349,0),(224,'','','USA',1356,0),(225,'','','Australia',1361,0),(226,'','','Africa',1365,0),(227,'','','United Kingdom',1370,1),(228,'34°48′000″N','005°41′000″E','',1397,0),(229,'48°28′018″N','020°29′044″E','',1401,0),(230,'24°56′000″N','075°76′000″E','',1425,0),(231,'24°55′000″N','075°79′000″E','',1426,0),(232,'24°55′000″N','075°75′000″E','',1427,0),(233,'25°01′016″S','047°55′031″W','',1471,0),(234,'23°20′036″S','045°07′044″W','',1474,0),(235,'32°54′012″N','106°52′045″E','Shaanxi Province: Hongsi Lake, Hanzhong',1569,0),(236,'41°07′045″N','008°40′007″W','Lavadores beach',1631,0),(237,'41°02′059″N','008°39′019″W','Portugal, Aguda beach',1632,0),(238,'41°07′045″N','008°40′007″W','Lavadores beach',1634,0),(239,'','','California',1636,0),(240,'31°03′302″S','050°02′809″W','',1637,0),(241,'12°46′015″S','045°17′017″E','Dziani Dzaha lake',1638,0),(242,'12°46′015″S','045°17′017″E','Dziani Dzaha lake',1640,0),(243,'12°46′015″S','045°17′017″E','Dziani Dzaha lake',1642,0),(244,'12°46′015″S','045°17′017″E','Dziani Dzaha lake',1643,0),(245,'25°15′035″N','107°42′047″E','Small Seven–hole Scenic Area, Guizhou province, China',1645,0),(246,'31°44′037″N','110°30′055″E','Shennongjia Forestry District, Hubei province',1647,0),(247,'06°29′027″N','003°23′049″E','',1649,0),(248,'29°18′059″S','071°14′055″W','',1651,0),(249,'34°02′029″N','116°08′042″W','',1652,0),(250,'39°57′004″N','024°41′006″E','',1654,0),(251,'39°57′004″N','023°41′006″E','',1655,0),(252,'39°57′004″N','023°41′006″E','',1656,0),(253,'09°29′058″N','083°30′024″W','',762,0),(254,'22°12′011″N','159°33′056″W','Kauai, Maniniholo 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River',2015,0),(272,'20°38′040″S','049°18′029″W','',2016,0),(273,'24°33′034″S','047°04′042″W','',2017,0),(274,'23°36′010″S','045°26′043″W','',2018,0),(275,'30°46′033″N','090°52′015″E','',2047,0),(276,'42°53′047″S','171°32′027″E','above the tree line in upper Otira Valley, Arthurs Pass National Park',2200,0),(277,'34°59′029″N','111°01′016″E','Yuncheng salt lake',2201,0),(278,'25°15′034″N','107°42′047″E','',2203,0),(279,'','','Queen Maud Land, Antarctica, nearby the Norwegian Meterological station',2204,0),(280,'','','Yaoundé',2205,0),(281,'17°29′003″N','092°02′042″W','Palenque ruins.',2206,0),(282,'19°24′054″N','155°14′013″W','Thurston Lava Tube, Hawaii Volcanoes National Park, Hawaii, USA',2207,0),(283,'21°21′057″N','157°47′027″W','Old Pali Highway, Island of Oahu, Hawaii',2211,0),(284,'','','hu Tho area, Tonkin, Vietnam',2215,0),(285,'','','Rice fields of Central Rice Research Institute, Cuttack, Orissa, India',2216,0),(286,'28°00′000″S','048°00′000″W','Tropical Atlantic Ocean, off Brazil',1392,0),(287,'','','Texas',2217,0),(288,'','','Chwaka, Zanzibar',2218,0),(289,'','','Five km north-west from Nikel town, Kola Peninsula, Russia,',2221,0),(290,'19°42′013″N','155°08′010″W','Akeola Road near Hilo, Hawaii',2222,0),(291,'40°27′008″N','011°46′057″E','',2223,0),(292,'78°39′005″N','016°20′014″E','',2225,0),(293,'37°49′045″N','111°25′013″W','',2226,0),(294,'46°35′015″N','014°07′059″E','',2227,0),(295,'36°24′015″N','025°23′045″E','',2228,0),(296,'35°30′014″N','115°41′032″W','',2229,0),(297,'34°03′056″N','116°10′013″W','',2230,0),(298,'27°50′049″S','071°00′034″W','',2231,0),(299,'37°18′017″N','127°02′003″E','',2232,0),(300,'48°53′042″N','014°56′011″E','',2233,0),(301,'22°47′000″N','073°43′000″E','',2234,0),(302,'53°28′024″N','006°08′032″E','',2235,0),(303,'78°56′058″N','011°28′036″E','',2236,0),(304,'26°06′040″S','070°32′055″W','',2237,0),(305,'25°16′005″N','082°59′030″E','',2238,0),(306,'44°54′034″N','015°36′031″E','',2250,0),(307,'25°27′054″N','080°20′006″W','',2252,0),(308,'20°16′003″N','098°54′058″W','',2253,0),(309,'19°20′013″N','097°21′019″W','',2254,0),(310,'40°42′012″N','141°18′000″E','',2255,0),(311,'27°12′037″N','097°26′021″W','',2259,0),(312,'27°51′000″N','097°25′000″W','',1119,0),(313,'40°12′032″N','008°25′038″W','Old Cathedral of Coimbra',2261,0),(314,'39°57′003″N','023°41′006″E','',2262,0),(315,'39°57′004″N','023°41′006″E','',2264,0),(316,'39°57′004″N','023°41′006″E','',2266,0),(317,'39°57′004″N','023°41′006″E','',2267,0),(318,'39°57′004″N','023°41′006″E','',2269,0),(319,'39°57′004″N','023°41′006″E','',2271,0),(320,'39°57′004″N','023°41′006″E','',2272,0),(321,'39°57′004″N','023°41′006″E','',2274,0),(322,'43°26′044″N','003°40′030″E','',2276,0),(323,'36°26′028″N','117°09′052″W','',2278,0),(324,'29°18′059″S','071°14′055″W','',2279,0),(325,'33°52′034″N','115°54′035″W','',2280,0),(326,'34°02′029″N','116°08′042″W','',2281,0),(327,'29°12′059″N','115°49′056″E','',2283,0),(328,'28°38′019″N','081°32′054″W','',2284,0),(329,'28°38′019″N','083°32′054″W','',2285,0),(330,'28°38′019″N','081°32′054″W','',2286,0),(331,'36°02′008″N','140°24′013″E','',2288,0),(332,'23°41′055″N','083°41′003″E','',2289,0),(333,'28°38′019″N','081°32′054″W','',2291,0),(334,'18°23′010″N','073°23′021″E','',2292,0),(335,'25°27′038″N','080°20′013″W','',2295,0),(336,'25°27′038″N','080°20′013″W','',2296,0),(337,'27°09′050″N','080°10′050″W','',2298,0),(338,'25°32′020″N','080°19′044″W','',2300,0),(339,'25°27′045″N','080°20′020″W','',2302,0),(340,'25°27′045″N','080°20′020″W','',2306,0),(341,'34°19′003″N','047°26′006″E','',2340,0),(342,'19°10′014″N','073°00′053″E','',2343,0),(343,'22°27′029″N','078°26′041″E','',2344,0),(344,'19°37′023″N','074°39′027″E','',2345,0),(345,'36°28′036″N','127°15′016″E','',2349,0),(346,'36°19′048″N','053°06′000″E','',2350,0),(347,'36°19′048″N','053°04′048″E','',2351,0),(348,'36°24′000″N','052°21′036″E','',2352,0),(349,'36°22′048″N','053°10′048″E','',2353,0),(350,'36°19′012″N','052°11′024″E','',2354,0),(351,'17°15′006″N','074°10′039″E','',2357,0),(352,'08°37′035″N','080°08′014″W','',2359,0),(353,'03°16′024″S','060°11′059″W','',2361,0),(354,'23°20′005″S','044°49′055″W','',2363,0),(355,'23°20′036″S','042°04′022″W','',2365,0),(356,'04°00′048″S','038°52′055″W','',1073,0),(357,'23°48′059″S','070°29′025″W','',2367,0),(358,'25°58′024″S','070°36′056″W','',2368,0),(359,'','','lake 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Francisco, California',2441,0),(407,'41°01′000″N','113°00′000″W','Great Basin Desert',2444,0),(408,'38°08′000″N','113°07′000″W','',2446,0),(409,'41°01′000″N','113°00′000″W','Great Basin Desert',2448,0),(410,'34°03′000″N','106°07′000″W','Chihuahuan Desert',2450,0),(411,'32°08′000″N','113°07′000″W','Sonoran Desert',2452,0),(412,'30°05′014″N','101°56′055″E','Ganzi Prefecture, Sichuan Province',2453,0),(413,'40°12′032″N','008°25′038″W','',2469,0),(414,'40°26′037″N','008°26′033″W','',2470,0),(415,'41°28′000″N','124°08′000″E','',2471,0),(416,'26°25′005″N','115°34′001″E','',2472,0),(417,'26°11′007″N','100°35′005″E','',2473,0),(418,'16°51′010″N','100°36′044″E','',2474,0),(419,'52°33′011″N','158°02′006″E','',2475,0),(420,'00°03′047″S','029°58′031″E','',2477,0),(421,'52°55′089″N','011°04′062″E','',2478,0),(422,'37°40′024″N','127°02′032″E','',2480,0),(423,'29°18′059″S','071°14′055″W','',2481,0),(424,'35°30′013″N','115°41′031″W','',2482,0),(425,'35°38′006″N','115°30′045″W','',2483,0),(426,'30°32′043″N','114°24′058″E','',2486,0),(427,'43°49′000″S','173°02′000″E','',2491,0),(428,'19°28′013″S','056°03′022″W','',2494,0),(429,'16°44′055″N','100°11′045″E','',2497,0),(430,'37°46′002″N','073°01′012″E','',2499,0),(431,'41°22′034″N','023°47′009″E','',2501,0),(432,'51°59′016″N','018°46′040″E','',2502,0),(433,'38°36′049″N','122°49′052″W','',2503,0),(434,'','','Fuerteventura',2509,0),(435,'24°24′046″N','092°08′029″E','',2512,0),(436,'30°05′014″N','101°56′055″E','',2514,0),(437,'24°19′022″N','092°00′022″E','',2516,0),(438,'48°39′012″N','002°01′029″W','',2517,0),(439,'32°48′023″N','075°32′036″E','',2519,0),(440,'21°20′006″N','157°48′058″W','',2520,0),(441,'20°48′034″N','156°36′018″W','',2522,0),(442,'49°06′000″N','014°09′000″E','',2523,0),(443,'68°37′012″N','149°38′008″W','',2533,0),(444,'68°46′037″N','149°39′008″W','',2534,0),(445,'68°36′047″N','148°51′004″W','',2535,0),(446,'68°38′042″N','149°34′052″W','',2536,0),(447,'68°37′015″N','149°39′042″W','',2537,0),(448,'68°37′049″N','149°38′032″W','',2539,0),(449,'11°26′007″N','107°25′025″E','',2542,0);
/*!40000 ALTER TABLE `cyanodb_gps` ENABLE KEYS */;
UNLOCK TABLES;

--
-- Table structure for table `cyanodb_images`
--

DROP TABLE IF EXISTS `cyanodb_images`;
/*!40101 SET @saved_cs_client     = @@character_set_client */;
/*!40101 SET character_set_client = utf8 */;
CREATE TABLE `cyanodb_images` (
  `id` int(11) NOT NULL AUTO_INCREMENT,
  `filename` char(255) COLLATE utf8_czech_ci NOT NULL,
  `description` text COLLATE utf8_czech_ci,
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INSERT INTO `cyanodb_images` VALUES (1,'acary_myiashi03.gif',NULL,0,'2017-08-28 19:37:14'),(2,'adrianema.jpg','Adrianema; from Komárek 1992',0,'2017-08-28 19:37:14'),(3,'albrightia.jpg','Albrightia; from Komárek (1992)',0,'2017-08-28 19:37:14'),(4,'alternatia.jpg','Alternantia; from Komárek 1992',0,'2017-08-28 19:37:14'),(5,'amatoidea.jpg','Ammatoidea; from Komárek 1992',0,'2017-08-28 19:37:14'),(6,'anabaena.jpg','Anabaena; from Komárek 1992',0,'2017-08-28 19:37:14'),(7,'anabaenopsis.jpg','Anabaenopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(8,'anabaenopsis_key_taylor1932.jpg','Anabaenopsis; key from Taylor (1932)  ',0,'2017-08-28 19:37:14'),(9,'aphanizomenon.jpg','Aphanizomenon; from Komárek (1992)',0,'2017-08-28 19:37:14'),(10,'aphanocapsa.jpg','Aphanocapsa; from Komárek 1992',0,'2017-08-28 19:37:14'),(11,'aphanothece.jpg','Aphanothece; from Komárek 1992',0,'2017-08-28 19:37:14'),(12,'arthronema.jpg','Arthronema; from Komárek 1992',0,'2017-08-28 19:37:14'),(13,'arthrospira.jpg','Arthrospira; from Komárek (1992)',0,'2017-08-28 19:37:14'),(14,'asterocapsa.jpg','Asterocapsa; from Komárek 1992',0,'2017-08-28 19:37:14'),(15,'aulosira.jpg','Aulosira; from Komárek (1992)',0,'2017-08-28 19:37:14'),(16,'bacularia.jpg','Bacularia; from Komárek 1992',0,'2017-08-28 19:37:14'),(17,'baradlaia.jpg','Baradlaia; from Komárek 1992',0,'2017-08-28 19:37:14'),(18,'baustriacastarm66.jpg','<i>Borzia austriaca</i>; from Starmach (1966: 366)',0,'2017-08-28 19:37:14'),(19,'blennothrix.jpg','Blennothrix; from Komárek (1992)',0,'2017-08-28 19:37:14'),(20,'borzia.jpg','Borzia; from Komárek 1992',0,'2017-08-28 19:37:14'),(21,'borzinema.jpg','Borzinema; from Komárek 1992',0,'2017-08-28 19:37:14'),(22,'brachytrichia.jpg','Brachytrichia; from Komárek (1992)',0,'2017-08-28 19:37:14'),(23,'brachytrichiopsis.jpg','Brachytrichiopsis; from Komárek (1992)',0,'2017-08-28 19:37:14'),(24,'braun05_fig1.jpg','Chroogloeocystis; from Brown et al. (2005) ',0,'2017-08-28 19:37:14'),(25,'braun05_fig2.jpg','Chroogloeocystis; from Brown et al. (2005) ',0,'2017-08-28 19:37:14'),(26,'braun05_fig5.jpg','Chroogloeocystis; from Brown et al. (2005) ',0,'2017-08-28 19:37:14'),(27,'braun05_fig7.jpg','Chroogloeocystis; from Brown et al. (2005) ',0,'2017-08-28 19:37:14'),(28,'cacuminatocrispadraw-kom-legntavera96.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Komárková-Legnerová & Tavera (1996: 416 sub <i>Cylindrospermopsis philippninensis</i>), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(29,'cacuminatocrispadraw1-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(30,'cacuminatocrispadraw2-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(31,'cacuminatocrispadraw3-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(32,'cacuminatocrispadraw4-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(33,'cacuminatocrispafoto-kom-legntavera96.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Komárková-Legnerová & Tavera (1996: 416 sub <i>Cylindrospermopsis philippninensis</i>)',0,'2017-08-28 19:37:14'),(34,'cacuminatocrispafoto1-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(35,'cacuminatocrispafoto2-coute04.jpg','<i>Cylindrospermopsis acuminato-crispa</i>; from Coute & Bouvy (2004)',0,'2017-08-28 19:37:14'),(36,'cafricanadraw-cronkom03.jpg','<em>Cylindrospermopsis africana</em>; from Cronberg &amp; Komárek (2003) sec. Komárek &amp; Komárková (2003) Komárek &amp; Kling (1996: 33) sec. Komárek &amp; Komárková (2003)',0,'2017-08-28 19:37:14'),(37,'cafricanadraw-komkling91.jpg','<i>Cylindrospermopsis africana</i>; from Komárek & Kling (1996: 33) sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(38,'cafricanafoto-komkling91.jpg','<i>Cylindrospermopsis africana</i>; from Komárek & Kling (1996: 42)',0,'2017-08-28 19:37:14'),(39,'calothrix.jpg','Calothrix; from Komárek 1992',0,'2017-08-28 19:37:14'),(40,'camptylonemopsis.jpg','Camptylonemopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(41,'capsosira.jpg','Capsosira; from Komárek 1992',0,'2017-08-28 19:37:14'),(42,'ccatemacodraw-kom-legntavera96.jpg','<i>Cylindrospermopsis africana</i>; from Komárková-Legnerová & Tavera(1996: 413), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(43,'ccatemacofoto-kom-legntavera96.jpg','<i>Cylindrospermopsis catemaco</i>; from Komárková-Legnerová & Tavera(1996: 415), sec. Komárek & Komárková (2003, pp)',0,'2017-08-28 19:37:14'),(44,'ccatemacotab-kom-legntavera96.jpg','<i>Cylindrospermopsis catemaco</i>; from Komárková-Legnerová & Tavera(1996: 413)',0,'2017-08-28 19:37:14'),(45,'ccfphilippninensisdraw1-komkomova02.jpg','<i>Cylindrospermopsis catemaco</i>; from Komárek & Komárková-Legnerová (2002: 228; sub Cylindrospermopsis cf. philippinensis), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(46,'ccurvispora-draw-mwatanabe95.jpg','<em>Cylindrospermopsis acuminato-crispa</em>; from Cronberg &amp; Komárek (2003), sec.Komárek &amp; Komárková (2003) M. Watanabe (1995), sec. Komárek &amp; Komárková (2003)',0,'2017-08-28 19:37:14'),(47,'ccurvispora-photo-mwatanabe95.jpg','<em>Cylindrospermopsis curvispora</em>; from M. Watanabe (1995)',0,'2017-08-28 19:37:14'),(48,'ccurvisporadraw-cronkom03.jpg','<i>Cylindrospermopsis curvispora</i>; from Cronberg & Komárek(2003), sec.Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(49,'ccuspisdraw-komkling96.jpg','<i>Cylindrospermopsis cuspis</i>; from Komárek & Kling (1996: 39), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(50,'ccuspisdraw-komkom03.jpg','<i>Cylindrospermopsis cuspis</i>; from Komárek & Komárková (2003, specimens from E Brazil)',0,'2017-08-28 19:37:14'),(51,'ccuspisfoto-komkling96.jpg','<i>Cylindrospermopsis cuspis</i>; from Komárek & Kling (1996: 43)',0,'2017-08-28 19:37:14'),(52,'chamaecalyx.jpg','Chamaecalyx; from Komárek 1992',0,'2017-08-28 19:37:14'),(53,'chamaesiphon.jpg','Chamaesiphon; from Komárek (1992)',0,'2017-08-28 19:37:14'),(54,'chelicoideadraw-cronkom03.jpg','<i>Cylindrospermopsis helicoidea</i>; from Cronberg & Komárek (2003), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(55,'chlorogleopsis.jpg','Chlorogloeopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(56,'chlorogloea.jpg','Chlorogloea; from Komárek (1992)',0,'2017-08-28 19:37:14'),(57,'chondrocystis.jpg',NULL,0,'2017-08-28 19:37:14'),(58,'chondrogloea.jpg','Chondrogloea; from Komárek 1992',0,'2017-08-28 19:37:14'),(59,'chroococcidiopsis.jpg','Chroococcidiopsis; from Komárek (1992)',0,'2017-08-28 19:37:14'),(60,'chroococcidium.jpg','Chroococcidium; from Komárek (1992)',0,'2017-08-28 19:37:14'),(61,'chroococcopsis.jpg','Chroococcopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(62,'chroococcus.jpg','Chroococcus; from Komárek (1992)',0,'2017-08-28 19:37:14'),(63,'chroogl_trom_brown05.gif','Chroogloeocystis; from Brown et al. (2005)',0,'2017-08-28 19:37:14'),(64,'clastidium.jpg','Clastidium; from Komárek (1992)',0,'2017-08-28 19:37:14'),(65,'clowei_casamatta_et_al_2006.gif','Capsosira; from Casamatta et al. 2006 ',0,'2017-08-28 19:37:14'),(66,'coelomoron.jpg','Coelomoron; from Komárek 1992',0,'2017-08-28 19:37:14'),(67,'coelosphaeriopsis.jpg','Coelosphaeriopsis; from Komárek (1992)',0,'2017-08-28 19:37:14'),(68,'coelosphaerium.jpg','Coelosphaerium; from Komárek (1992)',0,'2017-08-28 19:37:14'),(69,'coleodesmium.jpg','Coleodesmium; from Komárek 1989',0,'2017-08-28 19:37:14'),(70,'colteronema.jpg','Colteronema; from Komárek (1992)',0,'2017-08-28 19:37:14'),(71,'cphilippinensisdraw-hupes38.jpg','<i>Cylindrospermopsis philippinensis</i>; from Woloszynska (1912; coiled trichomes of <i>˝Anabaenopsis raciborskii˝</i>; possibly <i>C. philippinensis</i>, but compare also with coiled trichomes of <i>C. raciborskii</i> and with <i>C. acuminato-crispa</i>); sec. Huber-Pestalozzi (1938)',0,'2017-08-28 19:37:14'),(72,'cphilippinensisdraw-kom-ova98.jpg','<i>Cylindrospermopsis philippinensis</i>; from Komárková (1998; partly probably <i>C. acuminato-crispa</i>)',0,'2017-08-28 19:37:14'),(73,'cphilippinensisdraw-komkom03.jpg','<i>Cylindrospermopsis philippinensis</i>; from Komárek & Komárková (2003, fig. <b>d</b>  belongs probably to <i>C. acuminato-crispa</i>)',0,'2017-08-28 19:37:14'),(74,'cphilippinensisdrawtaylor32.jpg','<i>Cylindrospermopsis philippinensis</i>; from Taylor (1932; sub <i>Anabaenopsis philippinensis</i>); sec. Huber-Pestalozzi (1938)',0,'2017-08-28 19:37:14'),(75,'cracborskii_draw2_tox_ohtani1992.jpg','<i>Cylindrospermopsis raciborskii</i>; from Ohtani et al.(1992). For explanation see page 7941-2 l.c.',0,'2017-08-28 19:37:14'),(76,'cracborskii_draw_tox_ohtani1992.jpg','<i>Cylindrospermopsis raciborskii</i>; from Ohtani et al.(1992). For explanation see page 7941-2 l.c.',0,'2017-08-28 19:37:14'),(77,'craciborskii-draw-hill69.jpg','<i>Cylindrospermopsis raciborskii</i>; from Hill (1969)',0,'2017-08-28 19:37:14'),(78,'craciborskii-draw2-hill69.jpg','<i>Cylindrospermopsis raciborskii</i>; from Hill (1969)',0,'2017-08-28 19:37:14'),(79,'craciborskii-foto-hill69.jpg','<i>Cylindrospermopsis raciborskii</i>; from Hill (1969)',0,'2017-08-28 19:37:14'),(80,'craciborskii-mcgregor-graf1-00.jpg','<i>Cylindrospermopsis raciborskii</i>; mean +- SE cylindrospermopsin concentration for selected reservoirs (in SE Australia); from McGregor & Fabbro (2000)',0,'2017-08-28 19:37:14'),(81,'craciborskii-mcgrgor-map00.jpg','<i>Cylindrospermopsis raciborskii</i>; from distribution in NE Australia from McGregor & Fabbro, 2000',0,'2017-08-28 19:37:14'),(82,'craciborskii-mcgrgor-photo1-00.jpg','<i>Cylindrospermopsis raciborskii</i>; from McGregor & Fabbro (2000)',0,'2017-08-28 19:37:14'),(83,'craciborskii-mcgrgor-tab1.jpg','<i>Cylindrospermopsis raciborskii</i>; from McGregor & Fabbro 2000',0,'2017-08-28 19:37:14'),(84,'craciborskii-mcgrgor-tab2.jpg','<i>Cylindrospermopsis raciborskii</i>; from McGregor & Fabbro (2000)',0,'2017-08-28 19:37:14'),(85,'craciborskii-photo-kom-ova-99.jpg','<i>Cylindrospermopsis raciborskii</i>; from Komárková & al. (1999), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(86,'craciborskii-tab-eko-seenayya72.jpg','<i>Cylindrospermopsis raciborskii</i>; from Seenayya et Subba Raju 1972',0,'2017-08-28 19:37:14'),(87,'craciborskii-tab-tox-carmichel01.jpg','<i>Cylindrospermopsis raciborskii</i>; from Carmichael 2001',0,'2017-08-28 19:37:14'),(88,'craciborskii-tab1-kom-ova99.jpg',NULL,0,'2017-08-28 19:37:14'),(89,'craciborskii-tab2-kom-ova99.jpg',NULL,0,'2017-08-28 19:37:14'),(90,'craciborskii-tab3-kom-ova99.jpg',NULL,0,'2017-08-28 19:37:14'),(91,'craciborskii-tab4-kom-ova99.jpg',NULL,0,'2017-08-28 19:37:14'),(92,'craciborskii_draw2_couteetal97.jpg','<i>Cylindrospermopsis raciborskii</i>; from Coute et al. (1997: 59, 60)',0,'2017-08-28 19:37:14'),(93,'craciborskii_draw_couteetal97.jpg','<i>Cylindrospermopsis raciborskii</i>; from Coute et al. (1997: 59, 60)',0,'2017-08-28 19:37:14'),(94,'craciborskii_draw_geitler1932.jpg','<i>Cylindrospermopsis raciborskii</i>; from Geitler (1932) [ Probably  partly <i>C. philippinensis</i>  - see this species.]',0,'2017-08-28 19:37:14'),(95,'craciborskii_draw_padisak1990.jpg','<i>Cylindrospermopsis raciborskii</i>; from Padisák (1991; <i>sub Anabaenopsis raciborskii</i>)',0,'2017-08-28 19:37:14'),(96,'craciborskii_draw_proskina1968.jpg','<i>Cylindrospermopsis raciborskii</i>; from  Proškina-Lavrenko & Makarova (1968)',0,'2017-08-28 19:37:14'),(97,'craciborskii_eko2_saker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(98,'craciborskii_eko_couteetal97.jpg','<i>Cylindrospermopsis raciborskii</i>; from Coute et al. (1997: 60)',0,'2017-08-28 19:37:14'),(99,'craciborskii_eko_saker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(100,'craciborskii_foto2_saken1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(101,'craciborskii_foto_saken1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(102,'craciborskii_graf1_saker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(103,'craciborskii_tab2_saker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al. (1999)',0,'2017-08-28 19:37:14'),(104,'craciborskii_tab3_saker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al.(1999)',0,'2017-08-28 19:37:14'),(105,'craciborskii_tab_raker1999.jpg','<i>Cylindrospermopsis raciborskii</i>; from Saker et al.(1999)',0,'2017-08-28 19:37:14'),(106,'craciborskiidraw-bakerfabbro99.jpg','<i>Cylindrospermopsis raciborskii</i>; from Baker & Fabbro (1999: 34) sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(107,'craciborskiidraw-hind88.jpg','<i>Cylindrospermopsis raciborskii</i>; from Hindák (1988: 287)',0,'2017-08-28 19:37:14'),(108,'craciborskiidraw-singh62.jpg','<i>Cylindrospermopsis raciborskii</i>; from Singh (1962), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(109,'craciborskiidraw1-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Bruhl & Biswas (1922: 577; sub. <i>Cylindrospermum doryphorum</i>); sec. Desikachary (1959); Horecká & Komárek (1979), Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(110,'craciborskiidraw2-akom-ova1998.jpg','<i>Cylindrospermopsis raciborskii</i>; from Komárek (1984: 28); sec. Komárková (1998: 333), Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(111,'craciborskiidraw2-bkom-ova1998.jpg','<i>Cylindrospermopsis raciborskii</i>; from Horecká & Komárek (1979:300); sec. Komárková (1998:333), Komarek & Komárková (2003)',0,'2017-08-28 19:37:14'),(112,'craciborskiidraw2-kom79.jpg',NULL,0,'2017-08-28 19:37:14'),(113,'craciborskiidraw3-kom-ova99.jpg',NULL,0,'2017-08-28 19:37:14'),(114,'craciborskiidraw3a-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Singh (1969:..; sub <i>Anabaenopsis raciborskii</i>); sec. Kondrateva (1968; sub <i>Anabaenopsis koganii</i>), Horecká & Komárek (1979: 298)',0,'2017-08-28 19:37:14'),(115,'craciborskiidraw3b-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Kogan (1967:...sub <i>Anabaenopsis raciborskii</i>) sec. Obuchova in Obuchova & Kosenko (1964; sub <i>Anabaenopsis koganii</i>), Kondrateva (1968: 296), Horecká & Komárek (1979: 298), Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(116,'craciborskiidraw3ca-kom79.jpg',NULL,0,'2017-08-28 19:37:14'),(117,'craciborskiidraw3d-kom79.jpg',NULL,0,'2017-08-28 19:37:14'),(118,'craciborskiidraw3e-kom79.jpg',NULL,0,'2017-08-28 19:37:14'),(119,'craciborskiidraw4-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Skuja (1937: ...; sub. <i>Anabaenopsis raciborskii</i>); sec. Kondrateva (1968: 295), Horecká & Komárek (1979: 298), Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(120,'craciborskiidraw5-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Horecká & Komárek (1979: 301), Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(121,'craciborskiidrawkaufmannii-kom79.jpg','<i>Cylindrospermopsis raciborskii</i>; from Schmidle in Brunnthaler (1914: 223; sub <i>Aphanizomenon kaufmannii</i>); sec. Huber-Pestalozzi (1938; sub <i>Cylindrospermum ? Kaufmannii</i>), Horecká & Komárek (1979: 298), Komárek & Komárková (2003) ',0,'2017-08-28 19:37:14'),(122,'craciborskiigraf-dokulilmayer96.jpg','<i>Cylindrospermopsis raciborskii</i>; from Dokulil & Mayer (1996)',0,'2017-08-28 19:37:14'),(123,'craciborskiimap-dokulilmayer96.jpg','<i>Cylindrospermopsis raciborskii</i>; from Dokulil & Mayer (1996)',0,'2017-08-28 19:37:14'),(124,'craciborskiivarlongoscelldraw-komkom03.jpg','<i>Cylindrospermopsis raciborskii</i>; from Szalai (1942): <i>Anabaenopsis raciborskii var. longiscellula</i>: ....; sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(125,'cracibotskiitab1hill69.jpg','<i>Cylindrospermopsis raciborskii</i>; from Hill (1969)',0,'2017-08-28 19:37:14'),(126,'crinalium.jpg','Crinalium; from Komárek 1989',0,'2017-08-28 19:37:14'),(127,'croco_tree_zehr2001a.gif','Crocosphaera; tree from Zehr et al. (2001)  ',0,'2017-08-28 19:37:14'),(128,'crocosphaera_int.gif','Crocosphaera; taxon info from CMB',0,'2017-08-28 19:37:14'),(129,'crocosphaera_zehr&al.jpg',NULL,0,'2017-08-28 19:37:14'),(130,'cronbergia_key_kom2010.gif','Cronbergia; key from Komárek et al. (2010)',0,'2017-08-28 19:37:14'),(131,'cronbergia_reprod1_kom2010.gif','Cronbergia; from Komárek et al. (2010)',0,'2017-08-28 19:37:14'),(132,'cronbergia_reprod2_kom2010.gif','Cronbergia; from Komárek et al. (2010)',0,'2017-08-28 19:37:14'),(133,'cronbergia_tree_kom2010.gif','Cronbergia; tree from Komárek et al. (2010)  ',0,'2017-08-28 19:37:14'),(134,'csinuosadraw-coute03.jpg','<i>Cylindrospermopsis sinuosa</i>; from Coute et al. (2003:...), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(135,'csinuosadraw1-coute03.jpg','<i>Cylindrospermopsis sinuosa</i>; from Coute et al. (2003:...), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(136,'csinuosafoto-coute03.jpg','<i>Cylindrospermopsis sinuosa</i>; from Coute et al. (2003:...)',0,'2017-08-28 19:37:14'),(137,'csinuosafoto1-coute03.jpg','<i>Cylindrospermopsis sinuosa</i>; from Coute et al. (2003:...)',0,'2017-08-28 19:37:14'),(138,'ctaverae-kom02.jpg','<i>Cylindrospermopsis taverae</i>; from Komárek & Komárková-Legnerová(2002: 228), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(139,'cusp2005_draw1.gif','Cuspidothrix; from Rajaniemi et al. (2005) ',0,'2017-08-28 19:37:14'),(140,'cusp2005_draw2.gif','Cuspidothrix; from Rajaniemi et al. (2005) ',0,'2017-08-28 19:37:14'),(141,'cusp2005_tree.gif','Cuspidothrix; tree from Rajaniemi et al. (2005) ',0,'2017-08-28 19:37:14'),(142,'cusp2005_tree2.gif','Cuspidothrix; tree from Rajaniemi et al. (2005) ',0,'2017-08-28 19:37:14'),(143,'cyanoarbor.jpg','Cyanoarbor; from Komárek 1992',0,'2017-08-28 19:37:14'),(144,'cyanobacterium.jpg','Cyanobacterium; from Komárek 1989',0,'2017-08-28 19:37:14'),(145,'cyanobium.jpg','Cyanobium; from Komárek (1992)',0,'2017-08-28 19:37:14'),(146,'cyanobium_kom99.jpg','Cyanobium; ultrastructure from Komárek et al. (1999): C. gracile, type strain',0,'2017-08-28 19:37:14'),(147,'cyanobotrys.jpg','Cyanobotrys; from Komárek 1992',0,'2017-08-28 19:37:14'),(148,'cyanocatena.jpg','Cyanocatena; from Komárek (1992)',0,'2017-08-28 19:37:14'),(149,'cyanocatenula_joosten_2006.jpg','Cyanocatenula; from Joosten (2006: 35)',0,'2017-08-28 19:37:14'),(150,'cyanocomperia_hind_2002.jpg','Cyanocomperia; from Hindák (2002)',0,'2017-08-28 19:37:14'),(151,'cyanocystis.jpg','Cyanocystis; from Komárek (1992)',0,'2017-08-28 19:37:14'),(152,'cyanodermatium.jpg','Cyanodermatium; from Komárek 1992',0,'2017-08-28 19:37:14'),(153,'cyanodictyon.jpg','Cyanodictyon; from Komárek (1992)',0,'2017-08-28 19:37:14'),(154,'cyanogranis.jpg','Cyanogranis; from Komárek (1992)',0,'2017-08-28 19:37:14'),(155,'cyanokybus.jpg','Cyanokybus; from Komárek 1992',0,'2017-08-28 19:37:14'),(156,'cyanonephron.jpg','Cyanonephron; from Komárek (1992)',0,'2017-08-28 19:37:14'),(157,'cyanophanon.jpg','Cyanophanon; from Komárek (1992)',0,'2017-08-28 19:37:14'),(158,'cyanosaccus.jpg','Cyanosaccus; from Komárek 1992',0,'2017-08-28 19:37:14'),(159,'cyanosarcina.jpg','Cyanosarcina; from Komárek 1992',0,'2017-08-28 19:37:14'),(160,'cyanostylon.jpg','Cyanostylon; from Komárek 1992',0,'2017-08-28 19:37:14'),(161,'cyanotetras.jpg','Cyanotetras; from Komárek 1992',0,'2017-08-28 19:37:14'),(162,'cyanothamnos.jpg','Cyanothamnos; from Komárek 1992',0,'2017-08-28 19:37:14'),(163,'cyanothece.jpg','Cyanothece; from Komárek (1992)',0,'2017-08-28 19:37:14'),(164,'cylindrospermopsis.jpg','Cylindrospermopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(165,'cylindrospermopsis-key-kom-ova98.jpg','Cylindrospermopsis; key Komárková (1998)',0,'2017-08-28 19:37:14'),(166,'cylindrospermopsis-schembri01tox.jpg','<i>Cylindrospermopsis raciborskii</i>; from Schembri & al. (2001)',0,'2017-08-28 19:37:14'),(167,'cylindrospermopsis-tab-kom-ova98.jpg','Cylindrospermopsis; from Komárková (1998)',0,'2017-08-28 19:37:14'),(168,'cylindrospermopsis_graf_saker1999.jpg','Cylindrospermopsis; tree from Saker et al. (1999) ',0,'2017-08-28 19:37:14'),(169,'cylindrospermopsis_key2_kom02.jpg','Cylindrospermopsis; key from Komárek (2002: 35,36)',0,'2017-08-28 19:37:14'),(170,'cylindrospermopsis_key_kom02.jpg','Cylindrospermopsis; key from Komárek (2002: 35,36)',0,'2017-08-28 19:37:14'),(171,'cylindrospermopsisdraw-hind88.jpg','Cylindrospermopsis; from Hindák (1988)',0,'2017-08-28 19:37:14'),(172,'cylindrospermopsisdraw-kom79.jpg','Cylindrospermopsis; from Horecká & Komárek (1979)',0,'2017-08-28 19:37:14'),(173,'cylindrospermopsisdraw2kom_ova98.jpg','Cylindrospermopsis; from Komárková (1998); sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(174,'cylindrospermopsisdrawkom_ova98.jpg','Cylindrospermopsis; from Komárková (1998); sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(175,'cylindrospermopsiskey-komkom03.jpg','Cylindrospermopsis; key from Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(176,'cylindrospermopsiskladogram-kom79.jpg','Cylindrospermopsis; from Horecká & Komárek (1979)',0,'2017-08-28 19:37:14'),(177,'cylindrospermopsismap-komkom03.jpg','Cylindrospermopsis; map of distribution from Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(178,'cylindrospermopsismolecular-komkom03.jpg','Cylindrospermopsis; tree from Castenholz(2001, according to Saitou & Nei 1987 and Van de Peer & al. 1993), sec. Komárek & Komárková (2003)',0,'2017-08-28 19:37:14'),(179,'cylindrospermopsistab-coute03.jpg','Cylindrospermopsis; key from Coute et al. (2003)',0,'2017-08-28 19:37:14'),(180,'cylindrospermopsistaxondraw-komkom03.jpg','Cylindrospermopsis;  Komárek & Komárková (2003) ',0,'2017-08-28 19:37:14'),(181,'cylindrospermopsistaxondraw2-komkom03.jpg','Cylindrospermopsis; Komárek & Komárková (2003) ',0,'2017-08-28 19:37:14'),(182,'cylindrospermum.jpg','Cylindrospermum; from Komárek 1992',0,'2017-08-28 19:37:14'),(183,'dalmatella.jpg','Dalmatella; from Komárek 1992',0,'2017-08-28 19:37:14'),(184,'dermocarpella.jpg','Dermocarpella; from Komárek 1992',0,'2017-08-28 19:37:14'),(185,'desmosiphon.jpg','Desmosiphon; from Komárek 1992',0,'2017-08-28 19:37:14'),(186,'dichotrix.jpg','Dichotrix; from Komárek 1992',0,'2017-08-28 19:37:14'),(187,'doliocatella.jpg','Doliocatella; from Komárek 1992',0,'2017-08-28 19:37:14'),(188,'dzensia.jpg','Dzensia; from Komárek 1992',0,'2017-08-28 19:37:14'),(189,'enthophysalis.jpg','Enthophysalis; from Komárek 1992',0,'2017-08-28 19:37:14'),(190,'epigloeosphaera.jpg','Epigloeosphaera; from Komárek 1992',0,'2017-08-28 19:37:14'),(191,'epilithia.jpg','Epilithia; from Komárek 1992',0,'2017-08-28 19:37:14'),(192,'eucapsis.jpg','Eucapsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(193,'fiore_et_al07_tree1.gif','Brasilonema; tree from Fiore et al. (2007) ',0,'2017-08-28 19:37:14'),(194,'fischerella.jpg','Fischerella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(195,'fischerellopsis.jpg','Fischerellopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(196,'fortiea.jpg','Fortiea; from Komárek 1992',0,'2017-08-28 19:37:14'),(197,'gardnerula.jpg','Gardnerula; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(198,'geitleria.jpg','Geitleria; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(199,'geitleribactron.jpg','Geitleribactron; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(200,'geitleriella.jpg','Cyanoderma; from Komárek (1992), sub Geitleriella ',0,'2017-08-28 19:37:14'),(201,'geitlerinema.jpg','Geitlerinema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(202,'glaucospira.jpg','Glaucospira; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(203,'gleobacter.jpg','Gloeobacter; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(204,'gleocapsa.jpg','Gloeocapsa; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(205,'gloeocapsopsis.jpg','Gloeocapsopsis; from  Komárek 1992 ',0,'2017-08-28 19:37:14'),(206,'gloeothece.jpg','Gloeothece; from Komárek 1992',0,'2017-08-28 19:37:14'),(207,'gloeotrichia.jpg','Gloeotrichia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(208,'gomontiella.jpg','Gomontiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(209,'gomphosphaeria.jpg','Gomphosphaeria; from Komárek (1992) ',0,'2017-08-28 19:37:14'),(210,'halomic_abed02.jpg','Halomicronema; tree from Abed et al. (2002)  ',0,'2017-08-28 19:37:14'),(211,'halomic_abed02-2.jpg','Halomicronema; from Abed et al. (2002)  ',0,'2017-08-28 19:37:14'),(212,'halomic_ultra1.jpg','Halomicronema; ultrastructure from Abed et al. (2002)',0,'2017-08-28 19:37:14'),(213,'halomic_ultra2.jpg','Halomicronema; ultrastructure from Abed et al. (2002)',0,'2017-08-28 19:37:14'),(214,'halomic_ultra3.jpg','Halomicronema; ultrastructure from Abed et al. (2002)',0,'2017-08-28 19:37:14'),(215,'handeliella.jpg','Handeliella; from Komárek (1992) ',0,'2017-08-28 19:37:14'),(216,'hapalosiphon.jpg','Hapalosiphon; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(217,'hassallia.jpg','Hassallia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(218,'herpyzonema.jpg','Herpyzonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(219,'heterocyanococcus.jpg','Heterocyanococcus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(220,'heterolebleinia.jpg','Heteroleibleinia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(221,'hind_2002.jpg','Planktocyanocapsa; from Hindák (2002)  ',0,'2017-08-28 19:37:14'),(222,'hind_2002a.jpg','Planktocyanocapsa; from Hindák (2002)  ',0,'2017-08-28 19:37:14'),(223,'homeothrix.jpg','Homoeothrix; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(224,'homoeoptyche.jpg','Homoeoptyche; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(225,'hormoscilla.jpg','Hormoscilla; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(226,'hormothamnion.jpg','Hormothamnion; from Komárek 1992',0,'2017-08-28 19:37:14'),(227,'hormothece.jpg','Hormothece; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(228,'hydrococcus.jpg','Hydrococcus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(229,'hydrocoleum.jpg','Hydrocoleum; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(230,'hydrocoryne.jpg','Hydrocoryne; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(231,'hyella.jpg','Hyella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(232,'hypnomorpha.jpg','Hyphomorpha; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(233,'isocystis.jpg','Isocystis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(234,'iyengariella.jpg','Iyengariella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(235,'jaaginema.jpg','Jaaginema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(236,'johannesbaptistia.jpg','Johannesbaptistia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(237,'katagymene.jpg','Katagnymene; from Komárek (1992) ',0,'2017-08-28 19:37:14'),(238,'kyrtuthrix.jpg','Kyrtuthrix; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(239,'leibleinia.jpg','Leibleinia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(240,'lemmermanniella.jpg','Lemmermanniella; from Komárek 1992',0,'2017-08-28 19:37:14'),(241,'leptolyngbya.jpg','Leptolyngbya; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(242,'leptopogon.jpg','Leptopogon; from Komárek 1992',0,'2017-08-28 19:37:14'),(243,'letestuinema.jpg','Letestuinema; from Komárek 1992',0,'2017-08-28 19:37:14'),(244,'limnotrix.jpg','Limnothrix; from Komárek 1992',0,'2017-08-28 19:37:14'),(245,'lithococcus.jpg','Lithococcus; from Komárek 1992',0,'2017-08-28 19:37:14'),(246,'loefgrenia.jpg','Loefgrenia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(247,'loriella.jpg','Loriella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(248,'lyngbya.jpg','Lyngbya; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(249,'lyngbyopsis.jpg','Lyngbyopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(250,'macrospermum2_kom+ha2008.gif','Macrospermum; from Komárek 2008 ',0,'2017-08-28 19:37:14'),(251,'macrospermum_kom+ha2008.gif','Macrospermum; description by Komárek 2008 (orig.)',0,'2017-08-28 19:37:14'),(252,'mantellum.jpg','Mantellum; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(253,'mastigocladopsis.jpg','Mastigocladopsis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(254,'mastigocladus.jpg','Mastigocladus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(255,'mastigocoleopsis.jpg','Mastigocoleopsis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(256,'mastigocoleus.jpg','Mastigocoleus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(257,'matteia.jpg','Matteia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(258,'merismopedia.jpg','Merismopedia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(259,'microchaete.jpg','Microchaete; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(260,'microcoleus.jpg','Microcoleus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(261,'microcrocis.jpg','Microcrocis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(262,'microcystis.jpg','Microcystis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(263,'microcystis_dimorpha_kom+ha2008.jpg',NULL,0,'2017-08-28 19:37:14'),(264,'mojavia_rehakova2007.gif','Mojavia; from Řeháková et al. (2007) ',0,'2017-08-28 19:37:14'),(265,'myxohyella.jpg','Myxohyella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(266,'myxosarcina.jpg','Myxosarcina; from Komárek 1992',0,'2017-08-28 19:37:14'),(267,'nematoplaca.jpg','Nematoplaca; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(268,'nephrococcus.jpg','Nephrococcus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(269,'nodularia.jpg','Nodularia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(270,'nostoc.jpg','Nostoc; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(271,'nostochopsis.jpg','Nostochopsis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(272,'onkonema.jpg','Onkonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(273,'oscillatoria.jpg','Oscillatoria; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(274,'palikiella.jpg','Palikiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(275,'pannus.jpg','Pannus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(276,'paracapsa.jpg','Paracapsa; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(277,'parenchymorpha.jpg','Parenchymorpha; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(278,'parthasarathiella.jpg','Parthasarathiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(279,'pascherinema.jpg','Pascherinema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(280,'petalonema.jpg','Petalonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(281,'phormidiochaete_kom+ha2008.gif','Phormidiochaete by Komárek & Hauer (orig.)',0,'2017-08-28 19:37:14'),(282,'phormidiochaete_kom01.jpg','Phormidiochaete; from Anagnostidis (2001)  ',0,'2017-08-28 19:37:14'),(283,'phormidium.jpg','Phormidium; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(284,'placoma.jpg','Placoma; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(285,'planktolyngbya.jpg','Planktolyngbya; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(286,'plantothrix.jpg','Planktothrix; from Kommárek 1992 ',0,'2017-08-28 19:37:14'),(287,'plectonema.jpg','Plectonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(288,'pleurocapsa.jpg','Pleurocapsa; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(289,'podocapsa.jpg','Podocapsa; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(290,'proch_lewin75.jpg','Prochloron; from Lewin (1977: 155-156) ',0,'2017-08-28 19:37:14'),(291,'proch_lewin75_ultra.jpg','Prochloron; from Lewin (1975:157)',0,'2017-08-28 19:37:14'),(292,'proch_lewin75a.jpg','Prochloron; from Lewin (1977: 155-156) ',0,'2017-08-28 19:37:14'),(293,'prochlorococcus_caste2001.jpg','Prochlorococcus; light micrograph from Castenholz (2001: 507)',0,'2017-08-28 19:37:14'),(294,'protherendothrix.jpg','Proterendothrix; from Komárek 1992',0,'2017-08-28 19:37:14'),(295,'pseudanabaena.jpg','Pseudanabaena; from Komárek 1992',0,'2017-08-28 19:37:14'),(296,'pseudocapsa.jpg','Pseudocapsa; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(297,'pseudoncobyrsa.jpg','Pseudoncobyrsa; from Komárek 1992',0,'2017-08-28 19:37:14'),(298,'pseudophormidium.jpg','Pseudophormidium; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(299,'pseudoscytonema.jpg','Pseudoscytonema; from Komárek 1992',0,'2017-08-28 19:37:14'),(300,'pulvinularia.jpg','Pulvinularia; from Komárek 1992',0,'2017-08-28 19:37:14'),(301,'radaisia.jpg','Radaisia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(302,'radiocystis.jpg','Radiocystis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(303,'raphidopsis.jpg','Raphidiopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(304,'rerecta_casamatta_et_al_2006.gif','Rexia; from Casamatta et al. (2006) ',0,'2017-08-28 19:37:14'),(305,'rhabdoderma.jpg','Rhabdoderma; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(306,'rhabdogloea.jpg','Rhabdogloea; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(307,'rhodostichus.jpg','Rhodostichus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(308,'rholl53.jpg','Romeria; description by Hollerbach et al. (1953: 466)',0,'2017-08-28 19:37:14'),(309,'richeliageit42.jpg','Richelia; from Schmidt 1901, sec. Geitler 1942',0,'2017-08-28 19:37:14'),(310,'romeriadraw1.jpg','Rhabdoderma and Romeria; comparison of vegetation cycles, from Komárek (2001: 12,17-19 )',0,'2017-08-28 19:37:14'),(311,'romeriadraw2.jpg','Romeria; review of species from Komárek (2001: 12,17-19)',0,'2017-08-28 19:37:14'),(312,'romeriadraw3.jpg','Romeria; review of species from Komárek (2001: 12,17-19)',0,'2017-08-28 19:37:14'),(313,'romeriadraw4.jpg','Romeria; review of species from Komárek (2001: 12,17-19)',0,'2017-08-28 19:37:14'),(314,'romeriaelenkin49desc.jpg','Romeria; description by Elenkin (1949: 1427)',0,'2017-08-28 19:37:14'),(315,'romeriakey.jpg','Romeria; key from Komárek (2001: 16)',0,'2017-08-28 19:37:14'),(316,'romeriakeygeit32.jpg','Romeria; key from Geitler (1932: 915):  Sec. Elenkin (1949: 1427; in Russian)  ',0,'2017-08-28 19:37:14'),(317,'romeriakeyhind88.jpg','Romeria; key from Hindák (1988: 294-295)',0,'2017-08-28 19:37:14'),(318,'romeriakeyhind88a.jpg','Romeria; key from Hindák (1988: 294-295)',0,'2017-08-28 19:37:14'),(319,'romeriakeyhol53.jpg','Romeria; key from Hollerbach et al. (1953: 466-467)',0,'2017-08-28 19:37:14'),(320,'romeriakeyhol53a.jpg','Romeria; key from Hollerbach et al. (1953: 466-467)',0,'2017-08-28 19:37:14'),(321,'romeriakeystarm66.jpg','Romeria; key from Starmach (1966: 365)',0,'2017-08-28 19:37:14'),(322,'romeriakom03desc.jpg','Romeria; from Komárek, Sulek &amp; Hauer (2003)',0,'2017-08-28 19:37:14'),(323,'romeriakom03ultra.jpg','Romeria; ultrastucture from Komárek, Sulek et Hauer (2003)',0,'2017-08-28 19:37:14'),(324,'romeriakom70.jpg','Rhabdoderma and Romeria; vegetation cycles from Komárek (1970: 358)',0,'2017-08-28 19:37:14'),(325,'romeriakond68desc.jpg','Romeria; description by Kondrateva (1968: 74)',0,'2017-08-28 19:37:14'),(326,'romeriakond68eko.jpg','Romeria; from Kondrateva (1968: 74)',0,'2017-08-28 19:37:14'),(327,'schizothrix.jpg','Schizothrix; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(328,'schmidleinema.jpg','Schmidleinema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(329,'scytonema.jpg','Scytonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(330,'scytonematopsis.jpg','Scytonematopsis; from Komárek 1992',0,'2017-08-28 19:37:14'),(331,'seguenzaea.jpg','Seguenzaea; from Komárek 1992',0,'2017-08-28 19:37:14'),(332,'sinaiella.jpg','Sinaiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(333,'siphononema.jpg','Siphononema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(334,'siphonosphaera.jpg','Siphonosphaera; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(335,'sirocoleum.jpg','Sirocoleum; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(336,'snowella.jpg','Snowella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(337,'sokolovia.jpg','Sokolovia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(338,'solentia.jpg','Solentia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(339,'sphaerocavum_kom+ha2008.jpg','Sphaerocavum; from Komárek & Hauer orig. ',0,'2017-08-28 19:37:14'),(340,'spirirestis.jpg','Spiriestis; from Flechtner et al.(2002:8-10):',0,'2017-08-28 19:37:14'),(341,'spirirestis2.jpg','Spiriestis; from Flechtner et al.(2002:8-10):',0,'2017-08-28 19:37:14'),(342,'spirulina.jpg','Spirulina; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(343,'stanieria.jpg','Stanieria; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(344,'starria.jpg','Starria; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(345,'stauromatonema.jpg','Stauromatonema; from  Komárek 1992 ',0,'2017-08-28 19:37:14'),(346,'stigonema.jpg','Stigonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(347,'symphyonema.jpg','Symphyonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(348,'symphyonemopsis.jpg','Symphyonemopsis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(349,'symploca.jpg','Symploca; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(350,'synechococcus.jpg','Synechococcus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(351,'synechocystis.jpg','Synechocystis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(352,'thalpophila.jpg','Thalpophila; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(353,'thermosynechococcus_katoh_et_al2001.gif','Thermosynechococcus; as mentioned in Katoh et al, 2001',0,'2017-08-28 19:37:14'),(354,'thermosynechococcus_kom+ha2008.gif','Thermosynechococcus; from Komárek & Anagnostidis 1998 ',0,'2017-08-28 19:37:14'),(355,'thiochaete.jpg','Thiochaete; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(356,'tolypothrix.jpg','Tolypothrix; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(357,'trichodesmium.jpg','Trichodesmium; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(358,'trichormus.jpg','Trichormus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(359,'tubiella.jpg','Tubiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(360,'tychonema.jpg','Tychonema; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(361,'umezakia.jpg','Umezakia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(362,'voukiella.jpg','Voukiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(363,'westiella.jpg','Westiella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(364,'westiellopsis.jpg','Westiellopsis; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(365,'wollea.jpg','Wollea; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(366,'wolskyella.jpg','Wolskyella; from Komárek 1992  ',0,'2017-08-28 19:37:14'),(367,'woronichinia.jpg','Woronichinia; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(368,'xenococcus.jpg','Xenococcus; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(369,'xenotholos.jpg','Xenotholos; from Komárek 1994 ',0,'2017-08-28 19:37:14'),(370,'yonedaella.jpg','Yonedaella; from Komárek 1992 ',0,'2017-08-28 19:37:14'),(387,'35054-hi-pseudomonas.jpg',NULL,1,'2019-02-15 23:21:05');
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-- Table structure for table `cyanodb_sequences`
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CREATE TABLE `cyanodb_sequences` (
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) ENGINE=InnoDB AUTO_INCREMENT=911 DEFAULT CHARSET=utf8 COLLATE=utf8_czech_ci;
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INSERT INTO `cyanodb_synonyms` VALUES (1,'Cyanophyceae','Sachs 1874','','',NULL,0),(2,'Cyanophyta','Steinecke 1931','','',NULL,0),(3,'Actinocephalus','Kützing, Phyc. gen., p. 190-191.','','pre-starting-point syn.',NULL,0),(4,'Agmenellum','Brébisson, 1839. Mem. Soc. Acad. Sci., Arts, Bell.-Lett. Falaise, 1839: 2.',NULL,NULL,NULL,0),(5,'Ainactis','Kützing, 1843. Phycol. gener., p. 237.',NULL,'pre-starting-point syn.',NULL,0),(6,'Amalia','De Toni, 1934. Noter. nom. alg. 1: 5.',NULL,NULL,NULL,0),(7,'Amorphonostoc','Elenkin, 1936. Priroda 20(10): 969-970.',NULL,'probably special subgenus or genus',NULL,0),(8,'Amphitrix','Kützing ex Bornet et Flahault, 1886. Ann. Sci. Nat. Bot. 7, 3: 343.',NULL,'pro parte trichali',NULL,0),(9,'Anabaenella','Welsh, 1964. Nova Hedwigia 7: 20.',NULL,'subg. ILYONEMA',NULL,0),(10,'Anabaenothrix','Randhawa, 1936. Proc. Ind. Acad. Sci. 3(B): 407.',NULL,NULL,NULL,0),(11,'Anabaina','Bory de Saint Vincent, 1822. Dict. Class, d´Hist. Nat. 1: 308.',NULL,NULL,NULL,0),(12,'Anacystis','Meneghini, 1837. Consp. Algol. Eugan., p. 324.',NULL,'type material; sensu auct. post.',NULL,0),(17,'Aplococcus','roze, 1896. J. Bot. 10: 319-323.',NULL,'?',NULL,0),(18,'Arthrosiphon','Kützing, 1845. Phyc. germ., p. 117.',NULL,'pre-starting-point syn.',NULL,0),(19,'Arthronema','Hassall, 1845. Brit. Freshw. Alg., p. 238.',NULL,'pre-starting-point syn.',NULL,0),(20,'Arthrotilum','Rabenhorst, 1865. Fl. Eur. Alg. 2, p. 230.',NULL,'?',NULL,0),(21,'Arturoa','Gonzalez-Guerrero, 1951. Anal. Jard. Bot. Madrid 10: 210.',NULL,'without sheaths',NULL,0),(22,'Askenasya','Möbius, 1887. Ber. Dtsch. Bot. Ges. 5: 56.',NULL,NULL,NULL,0),(23,'Bacillosiphon','Copeland, 1936. Ann. N. Y. Acad. Sci. 36: 66.',NULL,NULL,NULL,0),(24,'Beckia','Elenkin, 1938. Monogr. Alg. Cyanoph. URSS, pars. Spec. 1: 71.',NULL,NULL,NULL,0),(25,'Belmontia','Archibald, 1967. Nova Hedwigia 12(3-4): 532.',NULL,'later homonym to BELMONTIA E. H. F. Meyer, 1838 (Phaner.)',NULL,0),(26,'Belonia','Carmichael in Hookers, 1833. Brit. Fl. 2: 379.',NULL,'pre-starting-point syn.',NULL,0),(27,'Bichatia','Turpin, 1828, Mem. Mus. Hist. Nat. Paris 16: 162.',NULL,NULL,NULL,0),(28,'Brachynema','Ercegović, 1931. Acta Bot. Inst. Bot. Univ. Zagreb 6: 36.',NULL,'later homonym',NULL,0),(29,'Brachythrix','A. Braun in Rabenhorst, 1865. Fl. Eur. Alg. 2: 118.',NULL,NULL,NULL,0),(30,'Cagniardia','Trevisan, 1848. Sagg. Monogr. Alg. Coccot., p. 47.',NULL,'?',NULL,0),(31,'Camptylonema','Schmidle, 1900. Hedwigia 39: 181.',NULL,'later homonym',NULL,0),(32,'Campylotropium','Hortobagyi et Hilliard, 1965. Acta bot. hung. 11: 141.',NULL,'incl.',NULL,0),(33,'Catella','Alvik, 1934. Bergens Mus. Arbok 1934 (Naturw. Rekke 6): 37.',NULL,'incl.',NULL,0),(34,'Chamaenema','Kützing, 1833. Linnaea 8: 364.',NULL,'pre-starting-point syn.',NULL,0),(35,'Chamaesiphonopsis','Fritsch, 1929. New Phytol. 28: 193.',NULL,'incl.',NULL,0),(36,'Chalarctis','Kützing, 1843. Phycol. gener., p. 236.',NULL,'pre-starting-point syn.',NULL,0),(37,'Chroobacter','Pringsheim, 1953. Arch. Microbiol. 19: 361.',NULL,'incl.',NULL,0),(38,'Cirrosiphon','Duvigneaud et Symoens, 1949. Lejeunia 13: 86.',NULL,'possibly a special genus of Phormidiaceae',NULL,0),(39,'Clathrocystis','Henfrey, 1856. Trans. Microsc. Soc. London 2, 4: 53.',NULL,NULL,NULL,0),(40,'Coccochloris','Sprengel, 1807. Fl. Hal. Mant. 1: 14.',NULL,NULL,NULL,0),(41,'Coelocystis','Nägeli in Kützing, 1849. Spec. Alg., p. 209.',NULL,NULL,NULL,0),(42,'Coleodesmiopsis','Dutt, Datta et Gupta, 1982',NULL,NULL,NULL,0),(43,'Coleodesmiumopsis','Cryptog.Algol. 3: 180.',NULL,NULL,NULL,0),(44,'Coleodesmium','Borzi, 1879. N. Giorn. Bot. Ital. 11: 348.',NULL,'validis. of pre-starting-point name',NULL,0),(45,'Coleonema','Schousboe ex Bornet et Thuret, 1880. Not. alg. 2: 73-75.',NULL,'pro syn.',NULL,0),(46,'Coleospermum','Kirchner in Cohn, 1878. Kryptogamenfl. Schlesiens 2: 239.',NULL,NULL,NULL,0),(47,'Croatella','Ercegović, 1925. Acta Bot. Inst. R. Univ. Zagreb 1: 92.',NULL,'incl.',NULL,0),(48,'Cyanarcus','Pascher, 1914. Ber.',NULL,NULL,NULL,0),(49,'Cyanoderma','Hansgirg, 1890. Phys. algol. Mitt. Sitzungsb. kgl. böhm. Acad. 1890: 91.',NULL,NULL,NULL,0),(50,'Cyanogastrum','Schiller, 1956. Ergebn. Dtsch. Limnol. Venezuela-Exp. 1952, p. 203-204.',NULL,'probably special subgenus',NULL,0),(51,'Cyanohydnum','Copeland, 1936. Ann. N. Y. Acad. Sci. 36: 199.',NULL,'incl.',NULL,0),(52,'Cyanospira','Florenzano et al., 1985. Arch. Microbiol. 140: 305.',NULL,'subg. DOLICHOSPERMUM',NULL,0),(53,'Cyanothrix (1)','Schmidle, 1897. All. Bot. Ztschr. 3(3): 37.',NULL,NULL,NULL,0),(54,'Cyanothrix (2)','Gardner, 1926. Mem. N. Y. Bot. Garden 7: 30.',NULL,'later homonym',NULL,0),(55,'Cystocoleus','Thuret, 1875. Ann. Sci. Nat.-Bot. 6, 1: 376.',NULL,'pre-starting-point syn.',NULL,0),(56,'Dasyactis','Kützing, 1843. Phycol. gener., p. 239.',NULL,'pre-starting-point syn.',NULL,0),(57,'Desmarestella','Bory de Saint Vincent, 1824. Dict. class. Hist. Nat. 5: 438.',NULL,'pre-starting-point syn.',NULL,0),(58,'Desmonema','Berkeley et Thwaites ex Bornet et Flahault, 1886. Ann. Sci.Nat.-Bot. 7, 5: 126.',NULL,'later homonym',NULL,0),(59,'Dictyothrix','Kützing (1843) ex Forti, 1907. Syll. Myxoph., p. 308.',NULL,NULL,NULL,0),(60,'Dillwynella','Bory de Saint Vincent, 1891. Dict. class. 1: 593.',NULL,NULL,NULL,0),(61,'Diplocolon','Nägeli ex Bornet et Flahault, 1886. Ann. Sci. Nat.-Bot. 7, 5: 129.',NULL,'incl.',NULL,0),(62,'Diplocystis','Trevisan, 1848. Sagg. Monogr. Alg. Coccot., p. 40.',NULL,NULL,NULL,0),(63,'Diplonema','Borzi, 1917. N. Giorn. Bot. Ital. 24: 103.',NULL,'later homonym',NULL,0),(64,'Diplotrichia','J. Agardh, 1842. Alg. mar. medit. adriat., p. 10.',NULL,'pre-starting-point syn.',NULL,0),(65,'Dolichospermum','Thwaites in Ralfs, 1843. Ann. Nat. Hist. 11: 161.',NULL,'subgenus',NULL,0),(66,'Drilosiphon','Kützing, 1843. Phycol. gener., p. 214.',NULL,'pre-starting-point syn.',NULL,0),(67,'Echeverriopsis','Kufferath, 1929. Ann. crypt. exot. 2: 49.',NULL,NULL,NULL,0),(68,'Eleutheronema','Weber van Bosse in Borzi, 1914. N. Giorn. Bot. Ital. 21:354.',NULL,'nomen nudum',NULL,0),(69,'Endonema','Pascher, 1929; Jahrb. wiss. Bot. 70: 347.',NULL,'later homonym',NULL,0),(70,'Endospora','Gardner, 1927. Mem. N. Y. Bot. Garden 7: 27.',NULL,NULL,NULL,0),(72,'Fischera','S. H. Schwabe, 1837. Linnaea: 124.',NULL,'pre-starting-point syn.',NULL,0),(73,'Fremyella','De Toni, 1936. Noter. nom. alg., p. 9.',NULL,NULL,NULL,0),(74,'Gaillardotella','Mougeot, 1898. Stirpes vogesorhen. 8, nr. 796.',NULL,NULL,NULL,0),(75,'Geitleriella','De-Toni, 1936. Noter. Nomencl. Algol. 8: 5.',NULL,NULL,NULL,0),(76,'Geocyclus','Kützing, 1843. Phycol. gener., p. 235.',NULL,'pre-starting-point syn.',NULL,0),(77,'Glaucothrix','Kirchner in Cohn, 1878. Kryptogamenfl. Schlesiens 2: 229.',NULL,'pre-starting-point syn.',NULL,0),(78,'Gloeochlamys','Schmidle, 1899. Allg. Bot. Ztschr. 5: 192.',NULL,NULL,NULL,0),(79,'Godlewskia','Janczewski, 1883. Mem. Acad. Cracov. 11: 142.',NULL,'subgenus',NULL,0),(80,'Gonidium','Ehrenberg ex Meneghini, 1849. Linnaea 14: 213.',NULL,NULL,NULL,0),(81,'Haliarachne','Lemmermann, 1899. Abh. Maturw. Ver. Bremen 16: 353.',NULL,'incl.',NULL,0),(82,'Halospirulina','Nübel, Garcia-Pichel et Muyzer, 2000 Int. J. Syst. Evol. Microbiol. 50: 1265-1277',NULL,NULL,NULL,0),(83,'Heliotrichum','Wille ex Schütt, 1893. Pflanzenleben Hochsee, p. 39.',NULL,NULL,NULL,0),(84,'Heteractis','Kützing, 1843. Phycol. gener., p. 239.',NULL,'pre-starting-point syn.',NULL,0),(85,'Heterohormogonium','Copeland, 1936. Ann. N. Y. Acad. Sci. 36: 64.',NULL,NULL,NULL,0),(86,'Hilsea','Kirchner, 1879. Kryptogamenfl. Schlesiens 2: 239.',NULL,'pre-starting-point syn.',NULL,0),(87,'Holopedium','(Lagerheim) Lagerheim, 1893. Nuova Notarisia 4: 209.',NULL,NULL,NULL,0),(88,'Hormactis','Thuret, 1875. Ann. Sci. Nat.-Bot. 6, 1: 376.',NULL,'pre-starting-point syn.',NULL,0),(89,'Hormosiphon','Kützing, 1843. Phycol. gener., p. 209.',NULL,'pre-starting-point syn.',NULL,0),(90,'Hormothamnion','Grunow ex Bornet et Flahault, 1886. Ann. Sci. Nat. Bot., ser. 7, 7: 259.',NULL,NULL,NULL,0),(91,'Hydroepicoccum','De-Notaris, 1868. Erb. Crittog. Ital., ser. 2: 178.',NULL,NULL,NULL,0),(92,'Hyellococcus','Schmidle, 1905. Allg. Bot. Ztschr. 11: 64.',NULL,NULL,NULL,0),(93,'Hypheothrix (1)','Kützing, 1843. Phycol. gener., p. 229.',NULL,'pre-starting-point syn.',NULL,0),(94,'Hypheothrix (2)','(Gomont ex Gomont) Kirchner, 1898. In Engler & Prantl, Nat. Pflanzenfam. 1(1a): 67.',NULL,'now considered subgenus of Schizotrix',NULL,0),(96,'Inactis','Kützing, 1843. Phycol. gener., p. 202.; Thuret, 1875. Ann. Sci. Nar.-Bot. 6, 1: 375.',NULL,'pre-starting-point syn.',NULL,0),(98,'Inconia','Libert, 1826. Ann. Soc. Linn. Paris 5: 402.',NULL,'pre-starting-point syn.',NULL,0),(99,'Inomeria','Kützing, 1845. Phycol. german., p. 191.',NULL,'pre-starting-point syn.',NULL,0),(100,'Isactis','[Thuret 1875] ex Wolle 1887',NULL,NULL,NULL,0),(101,'Kuetzingina','Kuntze, 1898. Rev. Gener. Pl. 3(3): 411.',NULL,NULL,NULL,0),(103,'Lauterbornia','Pringsheim, 1968. Arch. Microbiol. 63: 1-6.',NULL,'incl.',NULL,0),(104,'Leibleinia (1)','Endlicher, 1836. Gen. plant., p. 5.; Meneghini, 1838, Cenni Algh., p. 31.',NULL,'pre-starting-point syn.',NULL,0),(106,'Leibleinia (2)','Kützing, 1843. Phycol. gener., p. 221.',NULL,'pre-starting-point syn.',NULL,0),(107,'Lemmermannia','Elenkin, 1933. Acta Inst. Bot. Acad. Sci. USSR, 2, 1: 26.',NULL,'later homonym',NULL,0),(108,'Leptobasis','Elenkin, 1915. Bull. Jard. Imp. Pierre le Grande 15: 21.',NULL,'later homonym',NULL,0),(109,'Leptochaete','Borzi ex Bornet et Flahault, 1886. Ann. Sci. Nat.-Bot. 7, 3:341.',NULL,'pro parte trichali',NULL,0),(110,'Limnanthe','Kützing, 1843. Linaea: 86.',NULL,'pre-starting-point syn.',NULL,0),(111,'Limnochlide','Kützing, 1843. Phycol. gener., p. 203.',NULL,'pre-starting-point syn.',NULL,0),(112,'Linckia (1)','Wiggers, 1780. Prim. Fl. Holsat. 94.',NULL,'pre-starting-point syn., mixed with Xanthophyceae ?',NULL,0),(113,'Linckia (2)','[“Mich.”] Roth, 1802. Neue Beitr. Bot. 1:297.',NULL,'pre-starting-point syn.',NULL,0),(114,'Linckiella','Gaillon, 1833. Tab. synopt. meth. gen. Nemazoaires, p. 29.',NULL,'pre-starting-point syn.',NULL,0),(115,'Lithonema','Ercegović, 1929. Ann. Protist. 2: 136.',NULL,'later homonym',NULL,0),(116,'Lophopodium','Kützing, 1849. Tab. phycol. 1: 45.',NULL,'pre-starting-point syn.',NULL,0),(117,'Lpp-group A','sensu Rippka et al., 1979. J. gener. Microbiol. 111: 29-34.',NULL,NULL,NULL,0),(118,'Lpp-group B','sensu Rippka et al., 1979. J. gener. Microbiol. 111: 29-34.',NULL,NULL,NULL,0),(119,'Lithocapsa','Ercegović, 1925. Acta Bot. Inst. Bot. Zagreb. 1: 82.',NULL,NULL,NULL,0),(120,'Lunoevia','Sukačev, 1908. J. Bot. Soc. Imp. Nat. St.-Petersb. 3: 124.',NULL,NULL,NULL,0),(121,'Mastichonema','Kützing, 1843. Phycol. gener., p. 232.',NULL,'pre-starting-point syn.',NULL,0),(122,'Mastigonema','S. H. Schwabe, 1833. Linnaea 11: 112.',NULL,'pre-starting-point syn.',NULL,0),(123,'Mazaea','Bornet et Grunow, 1881. Bull. Soc. Bot. Fr. 33: 287.',NULL,'pre-starting-point syn.',NULL,0),(124,'Monocapsa','Itzigsohn in Rabenhorst, 1853. Alg. exsicc., Dec. 27: 263.',NULL,NULL,NULL,0),(125,'Monormia','Berkeley, 1832. Glean. Brit. Alg., p. 46.',NULL,'pre-starting-point syn.',NULL,0),(126,'Myxoderma (1)','Hansgirg, 1890. Phys. algol. Mitt. Sitzungsb. kgl. bohm. Acad. 1890: 91.',NULL,NULL,NULL,0),(127,'Myxoderma (2)','Schmidle, 1901. Engl. Bot. Jahrb. 25: 216.',NULL,NULL,NULL,0),(128,'Nematonostoc','Nylander ex Elenkin, 1934. Priroda 20(10): 969-970.',NULL,'incl.',NULL,0),(129,'Nematoradaisia','Geitler, 1925. Beih. Bot. Centrabl. 41 (2): 242',NULL,NULL,NULL,0),(130,'Neoadelia','Bompard, 1867. Hedwigia 6: 129.',NULL,'pre-starting-point syn.',NULL,0),(131,'Nostochium','Link in Nees, 1820. Hor. Phys. Berol, p. 6.',NULL,'pre-starting-point syn.',NULL,0),(132,'Oncobyrsa','Meneghini, 1842. Atti R. Accad. Sci. Torino, ser. 2, 5: 95.',NULL,NULL,NULL,0),(133,'Pelagothrix','J. Schmidt, 1901. Vidensk. Medd. Nat. Foren. Kjobenhavn, p. 144.',NULL,NULL,NULL,0),(134,'Physactis','Kützing, 1843. Phycol. gener. p. 235.',NULL,NULL,NULL,0),(135,'Planosphaerula','Borzi, 1905. Nuova Notarisia, ser. 16: 20.',NULL,NULL,NULL,0),(136,'Plaxonema','Tangl, 1883. Denkschr. K. Akad. Wiss. Wien, mat.-nat., 48: 1.',NULL,'pre-starting-point syn.',NULL,0),(137,'Polycoccus','Kützing, 1841. Naturk. Verh. Holl. Maatch. Wetensch. Haarlem, Taf. Q.',NULL,'pre-starting-point syn.',NULL,0),(138,'Polycystis','(Kützing) Kützing, 1849. Spec. Alg., p. 210.',NULL,NULL,NULL,0),(139,'Polythrix','Zanardini ex Bornet et Flahault, 1886. Ann. Sci. Nat.-Bot. 7, 3: 380.',NULL,'later mononym',NULL,0),(140,'Portacus','Kuntze, 1891. Rev. Gener. 2: 911.',NULL,NULL,NULL,0),(141,'Pseudoholopedia','(Ryppowa) Elenkin, 1935. Monogr. Alg. Cyanoph. URSS 1: 539.',NULL,'incl.',NULL,0),(142,'Pseudonostoc','Elenkin, 1949. Monogr. Alg. Cyanoph. URSS, pars spec. 2: 1225.',NULL,'incl.',NULL,0),(143,'Pseudospelaeopogon','Elenkin, 1949. Monogr. Alg. Cyanoph. URSS, pars spec. 2: 1839.',NULL,'incl.',NULL,0),(144,'Raciborskia','Koczwara, 1928. Kosmos 53: 108.',NULL,'later homonym',NULL,0),(145,'Radaisiella','Geitler, 1925. Beih. Bot. Centralbl. 2, 41: 242.',NULL,'incl.',NULL,0),(146,'Rhodococcus','Hansgirg in Wittrock et Nordstedt, 1884. Alg. Exsicc. 14: 697.',NULL,'?',NULL,0),(147,'Rivulariopsis','(Kirchner) Voronichin, 1923. Bot. Mat. Inst. Spor. Rast. Gl. Bot. Sada Petrohrad 1(8): 115.',NULL,'subgenus?',NULL,0),(148,'Schizodictyon','Kützing, 1943. Phycol. gener., p. 230.',NULL,'pre-starting-point syn.',NULL,0),(149,'Schizosiphon','Kützing, 1843. Phycol. gener., p. 233.',NULL,'pre-starting-point syn.',NULL,0),(150,'Sclerothrix','Kützing, 1833. Alg. Aq. dulc., Dec. 2. no. 17.',NULL,'pre-starting-point syn.',NULL,0),(151,'Scopulonema','Ercegović, 1930. Arch. Protistenk. 71: 365.',NULL,NULL,NULL,0),(152,'Setchelliella','De-Toni, 1936. Noter. nom. alg. 8: 6.',NULL,NULL,NULL,0),(153,'Siphoderma','Kützing, 1843. Linnaea 17: 220.',NULL,'pre-starting-point syn.',NULL,0),(154,'Sirosiphon','Kützing, 1843. Phycol. gener., p. 219.',NULL,'pre-starting-point syn.',NULL,0),(155,'Skujaella','De Toni, 1938. Diagn. Alg. nov. 1, 4: 397.',NULL,NULL,NULL,0),(156,'Sommierella','Borzi, 1917. N. Giorn. Bot. Ital. 24: 79.',NULL,'incl.',NULL,0),(157,'Sorospora','Hassall, 1845. Hist. Brit. Freshw. Algae 1: 309.',NULL,NULL,NULL,0),(158,'Spermosira','Kützing, 1843. Phycol. gener., p. 213.',NULL,'pre-starting-point syn.',NULL,0),(159,'Sphaenosiphon','Reinsch, 1874/1875. Contr. alg. fung., p. 15.',NULL,'?',NULL,0),(160,'Sphaerodictyon','Geitler, 1925. Beih. Bot. Centralbl. 2, 41: 231.',NULL,NULL,NULL,0),(161,'Sphaerogonium','Rostafinski, 1883. R. Akad. Krak. 10: 280.',NULL,NULL,NULL,0),(162,'Sphaeronema','Umezaki, 1961. Mem. Coll. Agric. Kyoto Univ., 83: 31.',NULL,'later homonym',NULL,0),(163,'Sphaeronostoc','Elenkin, 1936. Priroda 20(10): 969-970.',NULL,'incl.',NULL,0),(164,'Sphaerospermum','Zapomělová, Jezberová, Hrouzek, Hisem, Řeháková et Komárková, 2009. Journal of Phycology 45: 1370',NULL,NULL,NULL,0),(165,'Sphaerozyga','C. A. Agardh, 1827. Flora 10, 2: 634.',NULL,'pre-starting-point syn.',NULL,0),(166,'Sphinctosiphon','G. S. West, 1907. Linn. Soc. J.-Bot. 38: 145.',NULL,'syn. after orig. fig.',NULL,0),(167,'Spirillopsis','Naumann, 1921. K. Sv. Vet.-Acad. Handl. 62(4): 18.',NULL,'incl.',NULL,0),(168,'Spirillum','Hassall, 1845. Brit. Freshw. Alg., p. 279.',NULL,'pre-starting-point syn.',NULL,0),(169,'Spirocoleus (1)','Möbius, 1889. Hedwigia 28: 312.',NULL,'pre-starting-point syn. for Leptolyngbya',NULL,0),(171,'Spirocoleus (2)','Möbius ex Crow, 1927. Trans. Amer. Microsc. Soc. 46(2): 147.',NULL,'sensu Crow, non sensu Möbius',NULL,0),(172,'Spirulinopsis','Bharadwaja, 1963. Proc. Ind. Acad. Sci. 57B(4): 248.',NULL,'?',NULL,0),(173,'Spilocapsa','Ley, 1947. Bot. Bull. Acad. Sinica 1: 77.',NULL,'?',NULL,0),(174,'Stratonostoc','Elenkin, 1936. Priroda 20(10): 969-970.',NULL,'incl.',NULL,0),(175,'Symphyosiphon','Kützing, 1843. Phycol. gener., p. 218.',NULL,'pre-starting-point syn.',NULL,0),(176,'Symphyothrix','Kützing, 1843. Phycol. gener., p. 200.',NULL,'pre-starting-point syn.',NULL,0),(177,'Thackerella','Bharadwaja, 1963. Proc. Ind. Acad. Sci. 57, b4: 254.',NULL,NULL,NULL,0),(178,'Thaumaleocystis','Trevisan, 1848. Alghe Coccot., p. 79.',NULL,NULL,NULL,0),(179,'Tildenia','Kosinskaja, 1926. Not. Syst. Inst. Crypt. Horti Bot. Pr. USSR 4: 85.',NULL,'later homonym',NULL,0),(180,'Trichophora','Bonnemaison, 1822. J. Phys. 94: 176?.',NULL,'pre-starting-point syn.',NULL,0),(181,'Trichormus','Allmann, 1843. Ann. Nat. Hist. 9: 161.',NULL,'pre-starting-point syn.',NULL,0),(182,'Undina','Fries, 1825. Syst. orb. veg. I, Pl. Homon., p. 348.',NULL,'pre-starting-point syn.',NULL,0),(183,'Vaginaria','Gray, 1821. Nat. Arr. Brit. Pl. 1: 280.',NULL,'pre-starting-point syn.',NULL,0),(184,'Vanhoeffenia','Wille, 1928. Dtsch. Südpolar-Exp. 1901-03, 8: 422.',NULL,'?',NULL,0),(185,'Xanthotrichum','Wille ex Schütt, 1893. Pflanzenleben Hochsee, p. 39.',NULL,NULL,NULL,0),(186,'Zonotrichia','J. Agardh, 1842. Alg. mar. medit. adriat., p. 9.',NULL,'pre-starting-point syn.',NULL,0),(188,'Johansenia','Hašler et al. 2014, Preslia 86: 81-94',NULL,'nom. illeg.',NULL,0),(231,'Leptolyngbya badia','Johansen et Lowe 2008. Algological Studies 126: 26',NULL,NULL,NULL,0),(232,'Leptolyngbya lurida (Gomont)','Anagnostidis &amp; Komárek 1988. Algolog. Stud. 80: 392',NULL,'',NULL,1),(233,'Leptolyngbya fontana (Hansgirg)','Komárek in Anagnostidis 2001, Preslia, Praha 73: 374',NULL,'',NULL,0),(234,'Leptolyngbya edaphica','(Elenkin) Anagnostidis &amp; Komárek in Anagnostidis 2001, Preslia 73: 366',NULL,'',NULL,0),(235,'Lyngbya lagerheimii f. edaphica','Elenkin 1949, Monographia algarum Cyanophycearum, p. 1577',NULL,'',NULL,0),(236,'Phormidium pseudacutissimum','(Geitler) Anagnostidis et Komárek, 1988. Arch. Hydrobiol. Suppl./Algol. Stud. 50–53: 404',NULL,'',NULL,0),(237,'Geitlerinema pseudacutissimum','(Geitler) Anagnostidis, 1989. Plant. Syst. Evol. 164: 43',NULL,'',NULL,0),(238,'Phormidium amphibium','(Agardh ex Gomont) Anagnostidis et Komárek, 1988. Algolog. Stud. 50–53: 404',NULL,'',NULL,0),(239,'Oscillatoria amphibia f. contorta','West G.S. 1909. &nbsp;J. Bot. 67: 243',NULL,'',NULL,0),(240,'Oscillatoria amphibia f. circinata','Anagnostidis, 1961. Ereynai Kyanoph. Therm. Ellados, p. 233',NULL,'',NULL,0),(241,'Geitlerinema amphibium','(Agardh ex Gomont) Anagnostidis, 1989. Plant. Syst. Evol. 164: 38',NULL,'',NULL,0),(242,'Phormidium carotinosum','(Geitler) Anagnostidis et Komárek, 1988. Algolog. Stud. 50–53: 404',NULL,'',NULL,0),(243,'Geitlerinema carotinosum','(Geitler) Anagnostidis, 1989. Plant. Syst. Evol. 164: 39',NULL,'',NULL,0),(244,'Geitlerinema tenue','(Anisimova) Anagnostidis, 2001. Preslia 73: 364',NULL,'',NULL,0),(245,'Lyngbya penicilliformis','Silva in Silva, Basson, &amp; Moe, 1996. University of California Publications in Botany 79:39',NULL,'',NULL,0),(246,'Anabaena compacta','(Nygaard) Hickel, 1985. Algological Studies 38/39:&nbsp; 269-270',NULL,'',NULL,0),(247,'Anabaena crassa','(Lemmermann) Komárková-Legnová &amp; Cronberg 1992, Algological Studies 67: 24-25',NULL,'',NULL,0),(248,'Anabaena danica','(Nygaard) Komárková-Legnerová &amp; Eloranta 1992, Algological Studies 67: 112',NULL,'',NULL,0),(249,'Anabaena longicellularis','(Pankow) Komárková-Legnerová et Eloranta, 1992. &nbsp;Algological Studies 67: 125',NULL,'',NULL,0),(250,'Anabaena flos-aquae var. laxa','<em>Skuja, 1956. Nova Acta Regiae Societatis Scientiarum Upsaliensis, Series 4</em>, 16(3): 78',NULL,'',NULL,0),(251,'Anabaena smithii','(Komárek) M. Watanabe, 1992. Bull. Nat. Sci. Mus., ser. B, 18(4): 131',NULL,'',NULL,0),(252,'Johansenia constricta','(Szafer) Hašler, Dvořák et Poulíčková 2014, Preslia 86: 84',NULL,'',NULL,0),(253,'Pseudanabaena constricta','(Szafer) Lauterborn, 1915. Verh. Natur. Med. Ver. Heidelberg 13: 437',NULL,'',NULL,0),(254,'Komvophoron constrictum','(Szafer) Anagnostidis et Komárek 1988, Algological Studies 50–53: 373',NULL,'',NULL,0),(255,'Anabaena constricta','(Szafer) Geitler 1925, In Pascher’s Süsswasserflora 12: 312',NULL,'',NULL,0),(256,'Palmella alpicola','Lyngbye, &nbsp;1819. <em>Tentamen hydrophytologiae danicae</em>, p. 206',NULL,'',NULL,0),(257,'Palmella montana','Agardh, 1824. Systema algarum, p. 15',NULL,'',NULL,0),(258,'Gloeocapsa shuttleworthiana','Kützing 1843. <em>Phycologia generalis</em>, p. 173',NULL,'',NULL,0),(259,'Sorospora montana','Hassall, 1845. <em>A history of the British freshwater algae</em>, p. 309',NULL,'',NULL,0),(260,'Protococcus magma','Brébisson, &nbsp;1835. <em>Mémoires de la Société Académique des Sciences, Artes et Belles-Lettres de Falaise</em> 1835: 40',NULL,'',NULL,0),(261,'Gloeocapsa magma','(Brébisson) Kützing, 1847. <em>Botanische Zeitung</em> 5: 17',NULL,'',NULL,0),(262,'Gloeocapsa magma var. simmeri','(Schmidle) Novácek ex Geitler, 1932. Kryptogamen-Flora von Deutschland, p. 1164',NULL,'',NULL,0),(263,'Chroococcus simmeri','Schmidle ex Geitler, 1932. Kryptogamen-Flora von Deutschland,198',NULL,'',NULL,0),(264,'Planktolyngbya circumcreta','(G.S.West) Anagnostidis &amp; Komárek, 1988, &nbsp;Algological Studies 80: 394',NULL,'',NULL,0),(265,'Phormidium lloydianum','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 405',NULL,'',NULL,0),(266,'Phormidium acuminatum','(Gomont) Anagnostidis et Komarek 1988, Algol. Stud. 50-53: 404',NULL,'',NULL,0),(267,'Planktothrix cryptovaginata','(Škorbatov) Anagnostidis et Komárek, 1988, Algol. Stud. 50–53: 416',NULL,'',NULL,0),(268,'Lyngbya robusta','(Parakutty) Komárek et Komárková–Legnerová, &nbsp;2007, Hoehnea 34(1): 55',NULL,'',NULL,0),(269,'Phormidium murrayi','(W. et G.S.West) Anagnostidis et Komárek, 1988, Algological Studies 50–53: 408',NULL,'',NULL,0),(270,'Microcoleus glaciei','Casamatta, Johansen, Vis et Broadwater, &nbsp;2005, J. Phycol. 41: 432–433',NULL,'',NULL,0),(271,'Chroococcus distans','(Smith) Komárková-Legnerová et Cronberg 1994',NULL,'',NULL,0),(272,'Chroococcus dispersus','(Keissler) Lemmermann 1904',NULL,'',NULL,0),(273,'Gloeocapsa minor f. dispersa','(Keissler) Hollerbach in Elenkin 1938',NULL,'',NULL,0),(274,'Acaryochloris marina','Miyashita et Chihara 2003. Journal of Phycology 39: 1249','[46]','does not meet requiremets of art. 8.4 of the ICN',501,1),(275,'Oscillatoria gebhardtiana','Claus 1962. Hydrobiologia 19(2): 199','[144]','null',531,1),(276,'Phormidium etoshii','Dadheech, Casamatta, Casper et Krienitz 2013. Fottea 13(2): 237','[153]','null',584,1),(277,'Tolypothrix roberti-lamyi','Bourrelly in Bourrelly & Manguin 1952, p. 151','[206]','null',784,1),(278,'Camptylonemopsis sennae','Komárek 2003, Preslia 75: 225','[28]','null',785,1),(279,'Lyngbya hieronymusii','Lemmermann  1905, Forschungsber. biol. Stat. Plőn 12: 146','[208]','null',797,1),(280,'Lyngbya birgei','G.M. Smith, 1916, Bull. Torrey Bot. Club 43(9): 482','[209]','null',801,1),(281,'Lyngbya cryptovaginata','Škorbatov 1923, Not. Syst. Inst. Crypt. Horti Petrop. 2(6): 88','[214]','null',802,1),(282,'Lyngbya hieronymusii f. robusta','Parakutty 1940, Proc. Ind. Acad. Sci. 11: 123','[210]','null',803,1),(283,'Calothrix balearica','Bornet et Flahault ex Bomet et Flahault 1886, Ann. Sci. Nat., VIl. Bot., 3: 348','','null',807,1),(284,'Homoeothrix fusca','Starmach 1934, Acta Soc. Bot Poloniae 11(3): 294-295','','null',811,1),(285,'Dichothrix nordstedtii','Bornet et Flahault ex Bornet et Flahault 1886, Ann. Sci. Nat., VIL Bot., 3: 374,','','null',812,1),(286,'Lyngbya bornetii','Zukal 1894, Ber. Deutsch. Bot. Gess. 12:: 260','[211]','null',823,1),(287,'Oscillatoria bourrellyi','Lund 1955, Hydrobiologia 7: 225','[212]','null',824,1),(288,'Oscillatoria decolorata','G.S. West 1892, J. Bot. 37: 263','','null',825,1),(289,'Oscillatoria exospira','Skuja 1956, Nova Acta Rec. Soc. Sci. Upsal., Ser. 4, 16(3): 55','[213]','null',826,1),(290,'Oscillatoria granulata','Gardner 1927, Mem. New York Bot. Gard. 7: 37','[215]','null',827,1),(291,'Oscillatoria griseo-violacea','Skuja 1956, Nova Acta Reg. Soc. Sci. Upsal., Ser. 4, 16(4): 55','[213]','null',828,1),(292,'Oscillatoria ingrica','Voronichin 1931, Acta Horti Bot. Acad. Sci. URSS 44: 225','','null',829,1),(293,'Oscillatoria rhodonema','Skuja 1964, Nova Acta Reg. Soc. Sci. Upsal., Ser. 4, 18(3):: 49','[216]','null',830,1),(294,'Oscillatoria exilis var. sequana','Couté 1979, Bull. Mus. Nat. Hist. Natur. Ser. 4, SEc. B, 1: 272','[217]','null',831,1),(295,'Oscillatoria bornetii f. tenuis','Skuja 1930, Acta Horti Bot. Univ Latv. 10(3): 18','','null',832,1),(296,'Plectonema africanum','Borge 1928, Hedwigia 68: 107','[219]','null',853,1),(297,'Plectonema batrachospermum','Starmach 1957, Acta Soc. Bot. Polon. 26(3): 568','[220]','null',854,1),(298,'Plectonema puteale f. edaphicum','Elenkin 1949, Monogr. Alg. Cyanoph. Pars spec. 2: 1782','','null',855,1),(299,'Plectonema flexuosum','Gardner 1927, Mem. N.Y. Bot. Gard. 7: 47','[215]','null',856,1),(300,'Plectonema fortii','Frémy 1930, Arch. Mot. Mem. 3(2): 171','[221]','null',857,1),(301,'Plectonema hansgirgii','Schmidle 1900, Hedwigia 39:: 186','[222]','null',858,1),(302,'Plectonema indicum','Dixit 1936, Proc. Ind. Acad, Sci. 3(1) : 99','[223]','null',859,1),(303,'Plectonema phormidioides',' Hansgirg ex Forti 1907, Syll. Myxoph. p. 493','','null',860,1),(304,'Plectonema purpureum','Gomont 1892, An. Sci. Nat. VII Bot. 16: 101','[145]','null',861,1),(305,'Plectonema radiosum','Gomont 1892, An. Sci. Nat. VII Bot, 16: 100','[145]','null',862,1),(306,'Plectonema tauricum','Voronichin 1932,    313','','null',863,1),(307,'Plectonema tenue','Thuret ex Gomont 1892, An. Sci. Nat. VII Bot. 16: 101','[145]','null',864,1),(308,'Plectonema boryanum f. hollerbachianum','Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1787','','null',865,1),(309,'Plectonema battersii','Gomont 1899, Bull. Soc. Bot. France 46: 36','[224]','null',866,1),(310,'Plectonema mucicola','An 1992, Fragm. Florist. Geobot. 37(2): 410','[225]','null',868,1),(311,'Plectonema purpureum f. pauciramosum','Anissimova in Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1798','[226]','null',869,1),(312,'Plectonema rhenanum','Schmidle 1897, Hedwigia 36: 19','[227]','null',870,1),(313,'Plectonema spelaeoides','Čado 1959, : 2','','null',871,1),(314,'Plectonema tatricum','Starmach 1963: 431','[228]','null',872,1),(315,'PLectonema polymorphum var, viridis','Schwabe 1960, Oster. Bot. Ztschr. 107(3-4): 291','[230]','null',873,1),(316,'Oscillatoria arnoldii','Kisselev 1927','','null',897,1),(317,'Oscillatoria mougeotiii var. clathrata','Skuja 1956, Nova Acta Reg. Soc. Sci. Upsal. 16(3): 58','[213]','null',898,1),(318,'Lyngbya compressa','Utermöhl 1925, Arch Hydrobiol. Suppl. 5: 285','[234]','null',899,1),(319,'Oscillaria geitleri','Kisselev 1927, Izv. Otd. Prikl. Ichtiol. nauč.-prom. Issled. 5(2): 280','','null',900,1),(320,'Oscillatoria mouegotii','Bory ex Gomont 1892, Ann. Sci. Nat. VII. Bot. 16: 230 ???','[235]','null',901,1),(321,'Oscillatoria ornata f. planctonica','Elenkin 1949, Monogr. Alg. Cyanoph., Pars Spec. 2: 1265','[226]','null',902,1),(322,'Oscillatoria perornata','Skuja 1949, Nova Acta Reg. Soc. Sci. Upsal. Ser. 4, 14(5): 47','','null',903,1),(323,'Oscillatoria prolifica','Gomont 1892, Ann. Sci. Nat.  VII, Bot., 16: 205','[235]','null',904,1),(324,'Oscillatoria rubescens','De Candolle ex Gomont 1892, An. Sci. Nat. Bot., ser. VII,  16: 204','[235]','null',905,1),(325,'Oscillatoria agardhii var. suspensa','Pringsheim 1965, Arch. Microbiol. 50: 402','','null',906,1),(326,'Oscillatoria zahidii','Faridi & Khalil 1974, Biologia (Pakistan) 20(1): 65','[236]','null',907,1),(327,'Oscillatoria agardhii var. isothrix','SKUJA, 1948,  Symb. bot. Upsal. 9(3): 49','[238]','null',908,1),(328,'Trichodesmium lacustre','Klebahn 1895, Flora 80: 271','[237]','null',909,1),(329,'Oscillatoria miyadii','Negoro 1943, Sci. Rep. Tokyo Bunrika Daigaku, Sect. B. No. 94: 80','','null',910,1),(330,'Oscillatoria agardhii','Gomont 1892, Ann. Sci Nat. VII Bot,  16: 205','[235]','null',911,1),(331,'Trichodesmium iwanoffianaum','Nygaard 1926, Vidensk. Medd. Dansk Naturh. Foren. 82: 21','[239]','null',913,1),(332,'Anabaena fuellebornii','Schmidle ????','','null',914,1),(333,'Anabaena mysorensis','Gonzalves et Kamat 1959, Hydrobiologia 13: 237','[240]','null',915,1),(334,'Anabaena unispora','Gardner 1927, Mem N.Y. Bot. Garden 7: 59','[215]','null',916,1),(335,'Anabaena volzii','Lemmermann 1906,  Abh. Nat. Ver. Bremen 18(1): 153','[242]','null',917,1),(336,'Nostoc muscorum','Agardh ex Bornet et Flahault 1888, Ann. Sc. Nat. 7th Ser: 7:200','','null',919,1),(337,'Anabaena siamensis','Antarikanonda 1985, Nova Hedwigia 41: 345','[243]','null',921,1),(338,'Cylindrospermum planctonicum','Cronberg 2003, Algolog. Stud. 109: 205','[244]','null',922,1),(339,'Anabaena flos-aquae','[Lyngb ye] Brébisson ex Bornet et Flahault 1888, Ann. Sci. Nat. Bot. VII, 7: 228','','null',924,1),(340,'Anabaena affinis',' Lemmermann 1898, Abh. Naturw. Ver. Bremen 14: 261','[245]','null',926,1),(341,'Anabaena akankoensis','M. Watanabe 2003, Bull. Natn. Sci. Mus.,Tokyo, Ser. B, 29: 9–13','[246]','null',928,1),(342,'Anabaena arctica','Kiselev 1932, Gosud. Hidrol. Inst., Issled. Morej SSSR 15: 98','[247]','null',929,1),(343,'Anabaena bituri','Cronberg et Komárek 2004, Nova Hedwigia 78: 75','[248]','null',931,1),(344,'Anabaena berezowskii','Usačev 1928, Tr. Sibir. Naučn. Ribochoz. Stan. Krasnojarsk 3(2): 32','','null',933,1),(345,'Anabaena bothai','Welsh 1961, Rev. de Biol. 2(3/4): 259–260','[249]','null',935,1),(346,'Anabaena caspica','Ostenfeld 1902, Vidensk. Medd. Naturh. Fören. Kjøbenhavn 1901: 138','','null',937,1),(347,'Anabaena circinalis','Rabenhorst ex Bornet et Flahault 1988, Ann. Sci. Nat. 7, Bot 7: 230','','null',939,1),(348,'Anabaena citrispora','M. Watanabe 1992, Bull. Nat. Sci. Mus., ser. B, 18(4): 124–126','[250]','null',941,1),(349,'Anabaena spiroides var. minima f. compacta','Nygaard 1949,  Kong. Danske Vidensk. Selsk., Biol. Skr. 7(1): 205','[251]','null',943,1),(350,'Anabaena spiroides var. crassa','Lemmermann 1898,  Bot. Centralbl. 76(5-6): 155','[252]','null',945,1),(351,'Anabaena curva',' Hill 1976,  Phycologia 15(1): 62','[253]','null',947,1),(352,'Anabaena viguieri var. danica','Nygaard 1949, Kong. Danske Vidensk. Selsk., Biol. Skr. 7(1): 212','[251]','null',949,1),(353,'Anabaena delicatula','Lemmermann 1898, Bot. Centralbl. 76: 155','[252]','null',951,1),(354,'Anabaena ellipsoides','Bolochoncev ex Woronichin 1931, Tr. Bot. Sada AN SSSR 44: 221','','null',953,1),(355,'Anabaena fallax','Komárek et Komárková-Legnerová 2002, Preslia 74: 223','[254]','null',955,1),(356,'Anabaena farciminiformis','Cronberg et Komárková-Legnerová 1988, Algolog. Stud. 50– 53: 278','[255]','null',957,1),(357,'Anabaena fusca','Hill 1976, Phycologia 15(1): 70','[253]','null',959,1),(358,'Anabaena halbfassii','Bachmann, Ber. Dtsch. Bot. Ges. 31: 187, 1913','','null',961,1),(359,'Anabaena helicoidea','Bernard 1908, Protococc. & Desmid. d’Eau Douce, p. 52','[256]','null',963,1),(360,'Anabaena heterospora','Nygaard 1949 Kong. Danske Vidensk. Selsk., Biol. Skr., 7(1): 195','[251]','null',965,1),(361,'Anabaena jacutica','Kiselev 1932, Gosud. Hidrol. Inst., Issled. Morej SSSR 15: 100','[247]','null',967,1),(362,'Anabaena lemmermannii','Richter in Lemmermann 1903, Forschungsber. Biol. Stat. Plön 10: 153','','null',969,1),(363,'Anabaena spiroides var. longicellularis','Pankow 1965, Limnologova  3(2): 163–172, 1965','[257]','null',971,1),(364,'Anabaena maxima','Cronberg et Komárek 2004, Nova Hedwigia 78(1/2): 77','[248]','null',975,1),(365,'Anabaena mendotae','Trelease 1889, Trans. Wisconsin Acad. Sci. 7: 123','[258]','null',978,1),(366,'Anabaena mucosa','Komárková-Legnerová et Eloranta 1992, Algolog. Stud. 67: 125–126','[259]','null',980,1),(367,'Anabaena nathii','Vasishta 1960, Res. Bull. (N.S.) Panjab Univ., 11(I–II): 67','[260]','null',982,1),(368,'Anabaena nygaardii','Cronberg et Komárek 2004, Nova Hedwigia 78: 77– 78','[248]','null',984,1),(369,'Anabaena perturbata','Hill 1976, Phycologia 15(1): 67','[261]','null',986,1),(370,'Anabaena planctonica','Brunnthaler, Sitzungsb. K. Akad. Wiss. Wien, mat.–nat., 112: 292, 1903','[262]','null',988,1),(371,'Anabaena pseudocompacta','M. Watanabe 1996, Bull. Nat. Sci. Museum, Ser. B, 22(3): 94','[263]','null',990,1),(372,'Anabaena sigmoidea','Nygaard 1949 Kong. Danske Vidensk. Selsk. Biol. Skr. 7(1): 199','[251]','null',992,1),(373,'Anabaena skujae-laxa','Komárek et Zapomělová 2007, Fottea 7(1): 27','[36]','null',994,1),(374,'Anabaena solitaria f. smithii','Komárek  in Komárek & Ettl 1958, Algolog. Studien p. 129','[264]','null',996,1),(375,'Anabaena solitaria','Klebahn 1895,  Flora 80: 270','[237]','null',998,1),(376,'Anabaena spiroides','Klebahn 1895, Flora 80: 268','[237]','null',1000,1),(377,'Anabaena torques-reginae','Komárek 1984, Acta Bot. Cubana 19: 14–16','[265]','null',1002,1),(378,'Anabaena viguieri','Denis et Frémy 1924, Bull. Soc. Linn. Normandie, Ser. 7, 6: 122','[266]','null',1004,1),(379,'Anabaena werneri','Brunnthaler 1903, Sitzungsb. K. Akad. Wiss. Wien, mat.–nat., 112(1): 292','[262]','null',1006,1),(380,'Anabaena zinserlingii','Kosinskaja 1929, Russ. Arch. Protistol. 8(3/4): 245, 248','','null',1008,1),(381,'Aphanothece clathrata','W. West in W. et G.S.West 1906. Trans. Roy, Irish Acad. 33(A): 111','[269]','null',1022,1),(382,'Microcystis minutissima','W.West 1912. Proc. Royal. Irish Acad. 31(16): 1-62','[271]','null',1024,1),(383,'Aphanothece stratus','Komárek et Cronberg 2001, Nova Hedwigia 73(1-2): 133','[267]','null',1026,1),(384,'Aphanothece bachmannii','Komárková-Legenerová et Crongberg 1994. Algolog. Stud. 72: 21','[272]','null',1027,1),(385,'Aphanothece bacteriosa','Komárek et Komárková-Legnerová 2007. Nova Hedwigia 84(1-2): 72','[35]','null',1028,1),(386,'Aphanothece smithii','Komárková-Legnerová et Cronberg 1994. Algolog. Stud. 72: 25','[272]','null',1029,1),(387,'Oscillatoria pseudacutissima','Geitler 1956. Österr. Bot. Zeitschr. 103(2–3): 343','[280]','null',1074,1),(388,'Oscillatoria amphibia','Agardh ex Gomont, 1892. Ann. Sci. Nat.–Bot. 16: 221','[235]','null',1075,1),(389,'Oscillatoria acutissima','Kufferath, 1914. Ann. Biol. Lac. 7: 264','[281]','null',1076,1),(390,'Oscillatoria carotinosa','Geitler, 1956. Österr. Bot. Zeitschr. 103(2–3): 342','[280]','null',1077,1),(391,'Oscillatoria deflexa','W. et G.S. West, 1911. Brit. Antarct. Exped. 1(7): 295','','null',1078,1),(392,'Geitlerinema epiphloeophyticum','Anagnostidis, 2001. Preslia 73: 364','[9]','icona typica Brühl & Biswas 1923, J. Dept. Sci. Calcutta Univ. 4: 3, pl. 1 5a-b, figura nostra 8',1080,1),(393,'Oscillatoria exilis',' Skuja, 1964. N. Acta Reg. Soc. Sci. Upsal. Ser. 4, 18(3): 51','[216]','null',1081,1),(394,'Oscillatoria ionica','Skuja, 1937. Hedwigia 77: 30','[283]','null',1082,1),(395,'Oscillatoria lacus–solaris','Campbell et Golubic, 1985. Algol. Stud. 38/39: 324–325','[284]','null',1083,1),(396,'Oscillatoria lemmermannii','Woloszynska, 1912. Bull. Int. Acad. Sci. Cracovie, mat.–nat., Ser. B, 1913: 687','[233]','null',1084,1),(397,'Oscillatoria amphibia f. tenuis','Anisimova in Elenkin, 1949. Monographia algarum 2: 1326','[226]','null',1085,1),(398,'Phormidium penicillatum','Gomont, 1893. Bulletin de la Société Botanique de France 40: 159','[287]','null',1088,1),(399,'Oscillatoria constricta','Szafer, 1910. Bull. Int. Acad. Sci. Cracovie, Mat-Nat Sci, ser. B: 164','[297]','null',1098,1),(400,'Lyngbya circumcreta','G.S.West, 1907. Journal of the Linnaean Society of London, Botany 38: 174','[307]','null',1104,1),(401,'Spirulina fusiformis','Voronichin 1934. Trudy Soveta Izucheniu Prirodnych Resursov, Ser. Sibirsk. 8: 182','[310]','null',1109,1),(402,'Arthrospira indica','Desikachary et Jeei Bai 1992. ETTA Nat. Symp., Madras: 15','[311]','null',1111,1),(403,'Arthrospira maxima','Setchell et Gardner 1917. Univ. Calif. Publ. Bot. 6: 377','[312]','null',1114,1),(404,'Phormidium corallyticum','Rützler et Santavy, 1983.  Marine Ecology 4: 301','[314]','null',1117,1),(405,'Schmidleinema cubanum','Folia Geobot. Phytotax., Praha, 24: 192','[321]','null',1132,1),(406,'Lyngbya aerugieo-caerulea','Gomont, Ann. Sci. nat. 7, Bot. 16 : 146, 1892','[235]','null',1136,1),(407,'Oscillatoria redekei','Van Goor 1918. Recl. Trav. bot. neerl. 15: 258','[329]','null',1147,1),(408,'Oscillatoria rosea','Utermöhl 1925. Arch. Hydrobiol., Suppl. 5: 285, nom. illeg.','','null',1148,1),(409,'Oscillatoria splendida','Greville ex Gomont 1892. Ann. Sci. Nat. Bot., ser. 7, 16: 244','[235]','null',1163,1),(410,'Phormidium lumbricale','Casamatta, Johansen, Vis et Broadwater 2005. Journal of Phycology 41(2): 431','[16]','null',1174,1),(411,'Oscillatoria lloydiana','Gomont, 1899, Bull. Soc. Bot. France 46: 39','[224]','null',1194,1),(412,'Oscillatoria acuminata','Gomont 1892, Ann. Sci. Nat. Bot., ser. 7, 16: 227','[235]','null',1195,1),(413,'Oscillatoria animalis','Agard ex Gomont 1892, Ann. Sci. Natur., Botanique, Série 7, 16: 227-228','[235]','null',1196,1),(414,'Oscillatoria chlorina','Kützing 1843,  Phycologia generalis, p. 185','[135]','null',1197,1),(415,'Oscillatoria cortiana','Meneghini, 1837, Coment. Med. Dot. Spongia 4: 326','[340]','null',1198,1),(416,'Oscillatoria formosa','Bory, 1827, Dict. Class. d´Hist. Nat. 12: 474','[341]','null',1199,1),(417,'Oscillatoria jasorvensis','Vouk, 1919,  Jugosl. Akad. Prirod. Istr.Hrvatske i Slovenie, Mat. Prir.Razr. 14: 128','','null',1200,1),(418,'Oscillatoria laetevirens','Crouan et Crouan, 1867, Fl. Finistére p. 112','[342]','null',1201,1),(419,'Oscillatoria okenii','Agardh, 1827, Flora oder Botanische Zeitung 10(40): 633-634','[343]','null',1202,1),(420,'Phormidium pavlovskoense','Elenkin, 1949, Monogr. Alg. Cyanoph. Aquidulc. Terr. URSS, Fasc. 2, 1501–1502','[226]','null',1203,1),(421,'Oscillatoria proteus','Skuja, 1949, N. Acta Reg. Soc. Sci. Upsal., ser. 4, 14(5): 48','[344]','null',1204,1),(422,'Anabaena bergii','Ostenfeld 1908, Scientific Results of the Aral Sea Expedition 8: 142','[345]','null',1205,1),(423,'Aphanizomenon ovalisporum','Forti 1911, Atti Mem. Accad. Agric. Sci. Lett., Arti Comm. Verona, Series IV 12:  3-5','[346]','null',1206,1),(424,'Anabaena bergii var. minor','Kiselev 1927, Bull. Sect. Ichthyol. appl. Etud. scient. -ind. (U)2, 279','[347]','null',1207,1),(425,'Lyngbya murrayi','W. et G.S.West,  1911, Brit. Antarct. Exp. 1: 289','','null',1208,1),(426,'Chroococcus limneticus','Lemmermann, Bot. Zentralbl. 76: 153, 1898','[252]','null',1213,1),(427,'Chroococcus cumulatus','Bachmann, 1921, Mitt. Naturf. Ges. Luzern 8: 11','','null',1215,1),(428,'Chroococcus limneticus var. distans','Smith 1916, Bull. Torrey Bot, Club 43:481','[353]','null',1218,1),(429,'Chroococcus minor var. dispersus','Keissler 1902, Verh. Zool. - Bot. Ges, Vien 52: 311','[355]','null',1221,1),(430,'Brachytrichia maculans','Gomont 1902. Bot. Tidskrift 24: 210','[356]','null',1222,1),(441,'Trichocoleus deserti','','','',NULL,1),(465,'Lyngbya hieronymusii','Lemmermann &nbsp;1905, Forschungsber. biol. Stat. Plőn 12: 146',NULL,NULL,NULL,0),(466,'Leptothrix aeruginea','Kützing 1843',NULL,'',NULL,0),(467,'Schizothrix aeruginea','(Kützing) Desikachary 1959, <em><em>Cyanophyta</em></em>. &nbsp;p 334',NULL,'in Desikachary false (Rabenhorst) Desikachary 1959',NULL,0),(468,'Lyngbya amplivaginata f. hyalina','Hollerbach 1935',NULL,'',NULL,0),(469,'Lyngbya amplivaginata f. edaphica','Elenkin 1949',NULL,'',NULL,0),(470,'Porphyrosiphon amplivaginatus','&nbsp;(Van Goor) Anagnostidis &amp; Komárek 1988',NULL,'',NULL,0),(471,'Lyngbya pseudoafricana','Iltis 1972, <em>Cahiers de l\' O.R.S.T.O.M. Série Hydrobiologie</em> 6(3-4): 215',NULL,'',NULL,0),(472,'Lyngbya angustissima','(West et West) Iltis &nbsp;1972, <em>Cahiers de l\' O.R.S.T.O.M. Série Hydrobiologie</em> 6(3-4): 215',NULL,'',NULL,0),(473,'Leptolyngbya angustissima f. major','(West &amp; West) Aysel 2005',NULL,'',NULL,0),(474,'Phormidium angustissimum f. majus','Frémy 1930',NULL,'',NULL,0),(475,'Lyngbya rivulariorum','Gomont sensu Skuja 1926, Acta Horti. Bot. Univ. Latv. 1: 176 (non orig.)',NULL,'',NULL,0),(476,'Phormidium bigranulatum f. brevicellulatum','Claus',NULL,'',NULL,0),(477,'Phormidium bigranulatum f. majus','Vasishta 1965, J. Bomb. Natur. Hist. Soc. 62(1): 110',NULL,'',NULL,0),(478,'Oscillatoria gloiophila','Grunow in Rabenhorst 1865, Flora Europ. Algarum, p. 98',NULL,'',NULL,0),(479,'Leptolyngbya borodinii','(Kongisser) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 390',NULL,'',NULL,0),(480,'Plectonema roseolum','Gomont 1892',NULL,'',NULL,0),(481,'Hypheothrix roseola','Richter 1879',NULL,'',NULL,0),(482,'Lyngbya roseola','Richter in Wittrock &amp; Nordstedt 1882',NULL,'',NULL,0),(483,'Phormidium cataractarum','Rabenhorst 1863, Kryptogamen-Flora von Sachsen, p. 83',NULL,'',NULL,0),(484,'Hypheothrix cataractarum','Nägeli in Kützing 1849, Species algarum, p. 269',NULL,'',NULL,0),(485,'Lyngbya cebennensis','(Gomont) Compère 1974, Bull. Jard. Bot. Belgique <a href=\'//Bot.Belgique\'></a>44(1-2): 18',NULL,'',NULL,0),(486,'Leptolyngbya lurida','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 392',NULL,'',NULL,0),(487,'Hypheothrix compacta','(Kützing) Rabenhorst 1865, Flora europaea algarum, p. 79',NULL,'',NULL,0),(488,'Leptothrix compacta','Kützing 1843, Phycologia generalis, p. 199',NULL,'',NULL,0),(489,'Lyngbya compacta var. symplociformis','Grunow ex Hansgirg 1892, Prodromus, p. 88',NULL,'',NULL,0),(490,'Leptolyngbya delicatula','(Compère) Anagnostidis 2001, Preslia 73: 366','[Anagnostidis K. 2001: ]','',NULL,0),(491,'Leptolyngbya diplosiphon','(Voronichin) Anagnostidis &amp; Komárek 1988','[Algolog. Stud. 50-53: 391]','',NULL,0),(492,'Leptolyngbya endolithica','(Ercegović) Anagnostidis et Komárek 1988, Algolog. Stud. 50-53: 391','','',NULL,0),(493,'Lyngbya erebi var. thermalis','Claus 1961, Internat. Rev. ges. Hydrobiol. 46(4):514-541','','',NULL,0),(494,'Lyngbya foveolarum','[Montagne] Hansgirg 1892, Arch. Naturwiss. Landes. Böhmen 8(4): 86','','',NULL,0),(495,'Phormidium foveolarum var. leptotrichoides','Hansgirg ex Forti 1907, Syloge Algarum, p. 222','','',NULL,0),(496,'Oscillatoria foveolarum','&nbsp;(Montagne) Hansgirg ex Hansgirg 1892, Arch. Naturwis. LAndesd. Böhmen 8(4): 86','','',NULL,0),(497,'Lyngbya foveolarum var. leptotrichoides','Hansgirg 1892, Arch. Naturwiss. Landsd. Böhmen 8(4): 86','','',NULL,0),(498,'Phormidium foveolarum f. maior','&nbsp;Elenkin 1915','','',NULL,0),(499,'Hypheothrix foveolarum','(Montagne) Rabenhorst 1865, Flora Europea Algarum, p. 77','','',NULL,0),(500,'Leptothrix foveolarum','Montagne 1849, Ann. Sci. Nat. Bot. 12: 287','','',NULL,0),(501,'Lyngbya fragilis','(Gomont) Compère 1974, Bull. Jard. Bot. &nbsp;NAt. Belg. 44(1/2): 18','','',NULL,0),(502,'Pseudanabaena frigida','(Fritsch) Anagnostidis 2001, Preslia 73: 360','','',NULL,0),(503,'Leptolyngbya gardneriana','Anagnostidis 2001, Preslia 73(4): 366','','',NULL,0),(504,'Phormidium glaciale f. longiarticulata','Wille 1928','','',NULL,0),(505,'Leptolyngbya golenkiniana','(Gomont) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391','','',NULL,0),(506,'Plectonema golenkinianum f. anisimovianum','Elenkin 1949, Monogr. algarum, Izd. AN SSSR','','',NULL,0),(507,'Plectonema golenkinianum f. anisimovianum','Elenkin 1949, Monogr. Algarum, Izd. AN SSSr','','',NULL,0),(508,'Phormidium gracile var. roseum','Lindstedt 1943, Flora mar. Cyanoph. schwed. Westküste','','',NULL,0),(509,'Glaucothrix gracillima','Zopf, Zur Morphol. der Spaltpflanzen T. 6, Hansgirg, Uiber den Polymorph, der Algen, T. 1, Wittr. et Nordst&nbsp;','','',NULL,0),(510,'Lyngbya gracillima var. phormidioides','Hansgirg 1892, Arch. Naturwiss. Durchfors. Böhmen 8(4): 108','','',NULL,0),(511,'Lyngbya gracillima','[Kützing] Hansgirg 1892, Aech. Naturwiss. Durchfors. Böhmen 8(4): 108','','',NULL,0),(512,'Phormidium halophilum','(Hansgirg ex Hansgirg) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 408','','',NULL,0),(513,'Lyngbya halophila var. fuscolutea','&nbsp;Hansgirg 1892, Arch. Naturwiss. Durchfors. Böhmen 8(4): 92','','',NULL,0),(514,'Lyngbya halophila f. fuscolutea','(Hansgirg ex Hansgirg) Poljansky 1953','','',NULL,0),(515,'Lyngbya tenuissima','&nbsp;(Nägeli) Hansgirg ex Hansgirg 1892, Arch. Naturwiss.Durchforsch.Böhmen 8(4): 86','','',NULL,0),(516,'Leptothrix tenuissima','Nägeli in Kützing 1849, Species Algarum, p. 265','','',NULL,0),(517,'Hypheothrix tenuissima','(Nägeli) Rabenhorst 1865, Flora europaea algarum,p.77','','',NULL,0),(518,'Leptolyngbya frigida','(Fritsch) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391','','',NULL,0),(519,'Leptolyngbya hollerbachiana','(Elenkin) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 391','','',NULL,0),(520,'Lyngbya jadertina','(Meneghini) Hansgirg 1889, <em>Österr. Bot. Zeitschr.</em> 39: 42','','',NULL,0),(521,'Hypheothrix jadertina','(Meneghini) Kützing ex Rabenhorst 1865, Flora Europea Algarum, p. 89','','',NULL,1),(522,'Leptothrix jadertina','(Meneghini) Kützing 1849, Phycologia generalis, p. 265','','',NULL,0),(523,'Hypheothrix jadertina','(Meneghini) Kützing ex Rabenhorst 1865, Flora Europea Algarum, p. 89','','',NULL,0),(524,'Oscillaria jadertina','Meneghini in Rabenhorst 1865, Flora Europea Algarum p. 89','','',NULL,0),(525,'Spirocoleus lagerheimii','Möbius 1889, Hedwigia 28: 312','','',NULL,0),(526,'Lyngbya lagerheimii f. minor','(Voronichin et Chachina) Elenkin 1949, Sinezelenyye vodorosli SSSR, p. 1577','','',NULL,0),(527,'Lyngbya lagerheimii f. lacerata','Prasad, Mehrotra &amp; Singh 1976','','',NULL,0),(528,'Lyngbya lagerheimii f. minor','Desikachary 1959, Cyanophyta p. 291','','',NULL,0),(529,'Lyngbya laminosa','(Gomont ex Gomont) Hansgirg 1892, Arch. naturwiss. Landesdurch. Böhmen 8(4): 88','','',NULL,0),(530,'Oscillaria laminosa','Agardh 1827, Flora oder Botanische Zeitung 10: 633','','',NULL,0),(531,'Leptothrix laminosa','(Agardh) Rabenhorst 1847, Deutschlands Kryptogamen-Flora, p. 79','','',NULL,0),(532,'Hypheothrix laminosa','(Agardh) Rabenhorst 1865, Flora Europea Algarum, p. 79','','',NULL,0),(533,'Lyngbya minuta','Lindstedt 1943, Flora mar. Cyanoph. schwed. Westküste, p. 68','','',NULL,0),(534,'Lyngbya kufferathii','DeToni 1934','','',NULL,0),(535,'Lyngbya gloiophila','Lemmermann 1899, Abh. Naturwiss. Ver. &nbsp;Bremen 16: 355','','',NULL,0),(536,'Leptolyngbya nigricans Komárek 2005','Komárek 2005, Suess. Mit. Eurpa 19/2, p. 235','','nomen nudum',NULL,1),(537,'Leptolyngbya nigricans','Komárek 2005, Suesswaserfl. Mitt. Europa 19/2, p. 235','','nomen nudum',NULL,0),(538,'Plectonema nostocorum f. discolor','Cedercreutz 1929, Memor. Soc. Fauna et Flora Fennica 5: 154','','',NULL,0),(539,'Leptothrix olivacea','Kützing 1847','','',NULL,0),(540,'Hypheothrix olivacea','(Kützing) Rabenhorst 1865','','',NULL,0),(541,'Phormidium orientale var. longiarticulatum','Halasz 1942','','',NULL,0),(542,'Lyngbya orientalis','(G.S.West) Compère 1974, Bull. Jard. Bot. Nat. Belgique 44: 18','','',NULL,0),(543,'Leptolyngbya pauciramosa','(Anissimova) Anagnostidis &amp; Komárek 1988, Algolog. STud. 50-53: 392','','',NULL,0),(544,'Schizothrix coriacea var. endolithica','Ercegovic 1925, Acta Bot. Inst. Bot. Univ. Zabrabensis 10: 85','','',NULL,0),(545,'Schizothrix perforans var. maior','Geitler 1928','','',NULL,0),(546,'Leptolyngbya polymorpha','(Schwabe) Anagnostidis 2001, Preslia 73: 367','','',NULL,0),(547,'Leibleinia polysiphoniae','&nbsp;(Frémy) Compère 1985, Bull. Jard. Bot. Nat. Belgique 55: 487','','',NULL,0),(548,'Phormidium valderianum f. pseudovalderianum','(Woronichin) Elenkin 1949, Monogr. Alg. Cyanop. Pars spec. 2: 1472','','',NULL,0),(549,'Leptothrix purpurascens','Kützing 1847, &nbsp;Bot. Zeit. 5: 220','','',NULL,0),(550,'Phormidium purpurascens var. circinatum','Virieux 1911','','',NULL,0),(551,'Phormidium purpurascens var. laminatum','Copeland 1936, Ann. N.Y. Acad. Sci. 36: 184','','',NULL,0),(552,'Oscillatoria purpurea','Hooker &amp; Harvey 1845, London J. Bot. 4: 297','','',NULL,0),(553,'Lyngbya scottii var. minor','Fritsch 1912, Nat. Antarct. Exped. 1901-4, 6: 29','','',NULL,0),(554,'Lyngbya scottii f. minor','(Fritsch) Elenkin 1949, Monographia algarum, p. 1600','','',NULL,0),(555,'Lyngbya scottii f. lomniczensis','(Kol) Elenkin 1949, Monographia Algarum, p. 1600','','',NULL,0),(556,'Lyngbya scottii f. ucrainica','Elenkin 1949, Monographia Algarum, p. 1600','','',NULL,0),(557,'Cylindrospermopsis','Seenayya et Subba Raju, 1972. Tax. Biol. Blue-green Alg. (Madras):&nbsp; 55.','','',NULL,0),(558,'Leptolyngbya distincta','(Schmidle) Anagnostidis &amp; Komárek 1988, Preslia 73: 391','','',NULL,0),(559,'Lyngbya martensiana var. distincta','Nordstedt ex Schmidle 1897','','',NULL,0),(560,'Lyngbya kuetzingii var. distincta','(Nordstedt) Lemmermann 1905','','',NULL,0),(561,'Hypheothrix subtilissima','(Kützing) Rabenhorst 1865, Flora europaea algarum, p. 77','','',NULL,0),(562,'Leptothrix subtilissima','Kützing 1847, Tabule phycologicae p. 40','','',NULL,0),(563,'Phormidium subtilissimum','Rabenhorst ex Levi-Morenos 1892','','',NULL,0),(564,'Phormidium detersum','Gomont 1892, Ann. Sci. Nat., Bot. 7, 15: 330','','',NULL,0),(565,'Oscillatoria tenerrima','[Kützing 1843] ex Prain 1905, Rec. Bot. Surv. India 3: 333','','',NULL,0),(566,'Oscillatoria thrix','Corda 1836, Almanach Carlsbad','','',NULL,0),(567,'Oscillatoria tenerrima var. nigricans','Hansgirg ex Drouet 1957','','',NULL,0),(568,'Lyngbya tenerrima var. marina','Hauck ex Hansgirg 1893','','',NULL,0),(569,'Lyngbya tenerrima var. kuetzingiana','Hansgirg ex Forti 1907, Sylloge Myxophycearum, p. 170','','',NULL,0),(570,'Anabaena tenuis','Meneghini 1837, Come. Med. Spongia 4: 329','','',NULL,0),(571,'Lyngbya comperei','Senna 1983, Taxon 32(3): 467','','',NULL,0),(572,'Lyngbya comperei','Senna 1983, Taxon 32(3): 467','','',NULL,0),(573,'Plectonema terebrans f. hansgirgiana','(Hansgirg) Forti 1907, Sylloge Myxophycearum, p. 498','','',NULL,0),(574,'Lyngbya limnetica','sensu Anagnostidis 1961, Cyanoph. Thermalalguellen Griechenl. p. 123-124','','',NULL,0),(575,'Phormidium tenue f. circinata','Frémy 1930','','',NULL,0),(576,'Phormidium tenue var. minus','Tiwari 1972','','',NULL,0),(577,'Lyngbya comperei f. chungii','&nbsp;(Gardner) Bourrelly 1984','','',NULL,0),(578,'Lyngbya lagerheimii','Gomont 1892 sensu Palik 1949 and Anagnostidis 1961','','',NULL,0),(579,'Lyngbya treleasii','(Gomont) Compère 1974, ​Bull. Jard. Bot. Nat. Belg.44(1/2): 19','','',NULL,0),(580,'Lyngbya valderiana','(Gomont) Compère 1974','','',NULL,0),(581,'Phormidium valderiae','(Delponte) Schmidle 1901','','',NULL,0),(582,'Phormidium valderianum f. medium','Elenkin 1949','','',NULL,0),(583,'Phormidium valderianum f. majus','Hollerbach 1934','','',NULL,0),(584,'Phormidium valderianum f. circinatum','Anagnostidis 1961','','',NULL,0),(585,'Phormidium valderianum var. tenue','Voronichin 1923','','',NULL,0),(586,'Phormidium valderianum f. tenue','(Voronichnin) Elenkin 1949','','',NULL,0),(587,'Phormidium valderianum var. longiarticulatum','Li 1984','','',NULL,0),(588,'Phormidium valderianum var. validum','Li 1984','','',NULL,0),(589,'Lyngbya valderiana','&nbsp;(Gomont) Hansgirg 1905','','',NULL,0),(590,'Phormidium tenuissimum','Voronichin 1930, Tr. Leningr. Obšč. Estestv. 60(3): 68','','',NULL,0),(591,'Lyngbya delicatula','Compère 1985, Bull. Jard. Bot. Nat. Belg. 55: 488','','',NULL,0),(592,'Phormidium weedii','(Tilden) Copeland 1936,<em>&nbsp;Ann. N. Y. Acad. Sci. 36:172</em>','','',NULL,0),(593,'Lyngbya weissi','(Drouet) Compère 1974, Bull. Jard. Bot. Nat. Belgique 44: 19','','',NULL,0),(594,'Leptolyngbya delicatula','(Compère) Anagnostidis 2001, Preslia 73: 366','','',NULL,0),(595,'Leptolyngbya delicatula','(Compère) Anagnostidis 2001, Preslia 73: 366','','',NULL,0),(596,'Arthrospira breviarticulata','Setchell &amp; N.L.Gardner 1918, Univ. Calif. Publ. Bot. 6: 466','','',NULL,0),(597,'Plectonema jaagii','Geitler 1942, Emgler &amp; Prantl, Vol. 1b: &nbsp;Schizophyta, p. 157','','',NULL,0),(598,'Porphyrosiphon kurzii','(Gomont) Drouet 1968, Proc. Acad. Nat. Sci. Philadelphia, Monogr. 15: 162','','',NULL,0),(599,'Sirocoleum amorphum','(Thwaites ex Gomont) I.Umezaki &amp; M.Watanabe 1994, Jap. J. Phycol. 42: 201','','',NULL,0),(600,'Porphyrosiphon animalis','(Agardh) Drouet 1968','','',NULL,0),(601,'Lyngbya ceylanica var. constricta','Frémy 1930','','',NULL,0),(602,'Lyngbya ceylanica var. hyalinia','Ley 1948','','',NULL,0),(603,'Lyngbya ceylanica var. bankurensis','Sinha &amp; Mukherjee 1984','','',NULL,0),(604,'Phormidium corbierei (Frémy) Anagnostidis 2001: 370','&nbsp;(Frémy) Anagnostidis 2001, Preslia 73: 370','','',NULL,0),(605,'Phormidium corbierei','&nbsp;(Frémy) Anagnostidis 2001, Preslia 73: 370','','',NULL,0),(606,'Lyngbya dendrobia f. lurida','Brühl et Biswas 1923','','',NULL,0),(607,'Lyngbya dendrobia var. skujae','&nbsp;Desikachary 1959','','',NULL,0),(608,'Scytonema kaernbachii','Hennings 1892','','',NULL,1),(609,'Lyngbya microscopica','Crouan &amp; Crouan ex Gomont 1892','','',NULL,0),(610,'Scytonema notarisii','Meneghini 1849','','',NULL,0),(611,'Lyngbya notarisii','(Meneghini) Wille 1884','','',NULL,0),(612,'Schizothrix notarisii','(Meneghini) Sampaio 1964','','',NULL,0),(613,'Porphyrosiphon notarisii var. canus','&nbsp;Baker &amp; Bold 1970','','',NULL,0),(614,'Porphyrosiphon notarisii var. maior','Gardner 1927','','',NULL,0),(615,'Porphyrosiphon notarisii var. minor','&nbsp;Li 1989','','',NULL,0),(616,'Porphyrosiphon notarisii','sensu Croasdal 1973','','',NULL,0),(617,'Porphyrosiphon martensianus','(Meneghini ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(618,'Porphyrosiphon miniatus','(Gomont) Drouet 1968','','',NULL,0),(619,'Spirulina miniata','Hauck 1878','','',NULL,0),(620,'Spirulina sp.','Umezaki 1961','','',NULL,0),(621,'Porphyrosiphon splendidus','(Greville ex Gomont) Drouet 1968','','',NULL,1),(622,'Porphyrosiphon splendidus','(Greville ex Gomont) Drouet 1968','','',NULL,0),(623,'Microcoleus versicolor','(Wartmann) Collins ex Forti 1907','','',NULL,0),(624,'Phormidium versicolor','[Wartmann in Rabenhorst 1861] ex Gomont 1892','','',NULL,0),(625,'Lyngbya versicolor f. edaphica','Elenkin 1949','','',NULL,0),(626,'Lyngbya versicolor var. undulata','Prasad, Mehrotra &amp; Singh 1976','','',NULL,0),(627,'Oscillatoria acuminata f. longe-attenuata','Geitler &amp; Ruttner 1935','','',NULL,0),(628,'Oscillatoria bornetii','(Zukal) Forti 1907','','',NULL,0),(629,'Phormidium exospirum','(Skuja) Anagnostidis 2001','','',NULL,0),(630,'Tychonema granulatum','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413','','',NULL,1),(631,'Tychonema granulatum','(Gardner) Anagnostidis &amp; Komárek 1988, Algolog. Stud. 50-53: 413','','',NULL,0),(632,'Tychonema griseo-violaceum','(Skuja) Anagnostidis &amp; Komárek 1988','','',NULL,0),(633,'Tychonema ingricum','(Woronichin) Anagnostidis &amp; Komárek 1988','','',NULL,0),(634,'Phormidium animale','(Agardh ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(635,'Oscillatoria cortiana','Meneghini ex Gomont 189','','',NULL,0),(636,'Phormidium cortianum','(Meneghini ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(637,'Oscillaria cortii','Kützing 1836','','',NULL,0),(638,'Phormidium chlorinum','(Kützing ex Gomont) Umezaki &amp; Watanabe 1994','','',NULL,0),(639,'Lyngbya chlorina','(Kützing) Hansgirg 1885','','',NULL,0),(640,'Oscillatoria chlorina var. perchlorina','&nbsp;Lauterborn 1915','','',NULL,0),(641,'Oscillatoria chlorina f. perchlorina','(Lauterborn) Elenkin 1949','','',NULL,0),(642,'Lyngbya amoena var. chlorina','(Kützing) Hansgirg ex Forti 1907','','',NULL,0),(643,'Phormidium formosum','(Bory ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(644,'Oscillatoria tenuis var. formosa','(Bory) Kützing ex Gomont 1892','','',NULL,0),(645,'Oscillaria meugeotii','Bory 1827','','',NULL,0),(646,'Oscillaria amphibia','Kützing 1836','','',NULL,0),(647,'Oscillaria cortiana','&nbsp;Richter in Wittrock et Nordstedt 1884','','',NULL,0),(648,'Phormidium gebhardtianum','(Claus) Anagnostidis &amp; Komárek 1988','','',NULL,0),(649,'Phormidium jasorvense','(Vouk) Anagnostidis &amp; Komárek 1988','','',NULL,0),(650,'Phormidium laetevirens','(Crouan &amp; Crouan ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(651,'Phormidium okenii','(Agardh ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(652,'Lyngbya cortiana','(Meneghini) Hansgirg 1892','','',NULL,0),(653,'Lyngbya okenii','(Agardh) Hansgirg 1884','','',NULL,0),(654,'Phormidium proteus','(Skuja) Umezaki &amp; Watanabe 1994','','',NULL,0),(655,'Planktothrix raciborskii','(Wołoszyńska) Anagnostidis et Komárek 1988','','',NULL,0),(656,'Microcoleus boergesenii','(Gardner) Frémy 1939','','',NULL,0),(657,'Schizothrix brebissonii','(Kützing ex Gomont) Bourrelly 1970','','',NULL,0),(658,'Microcoleus brebissonii','(Kützing) ex Hansgirg 1892','','',NULL,0),(659,'Microcoleus heterotrichus','[Kützing] Wolle ex Hansgirg 1892','','',NULL,1),(660,'Microcoleus brebissonii var. aerugineus','Rabenhorst ex Hansgirg 1892','','',NULL,0),(661,'Hydrocoleum bremii var. obscurum','Hansgirg 1891','','',NULL,0),(662,'Hydrocoleum bremii f. obscura','(Hansgirg) Poljanskij in Hollerbach &amp; al. 1953','','',NULL,0),(663,'Calothrix comoides','Harvey ex Bornet &amp; Flahault 1886','','',NULL,0),(664,'Hydrocoleum confluens','(Setchell &amp; Gardner) Drouet 1942','','',NULL,0),(665,'Capillus','Caires, Sant’Anna et Nunes 2018','','',NULL,0),(666,'Capillus salinus','Caires, Sant’Anna et Nunes 2018','','',NULL,0),(667,'Capillus tropicalis','Caires, Sant’Anna et Nunes 2018','','',NULL,0),(668,'Microcoleus floccosus (Hauck) Hauck 1885','(Hauck) Hauck 1885','','',NULL,0),(669,'Oscillatoria floccosa','Hauck 1876','','',NULL,0),(670,'Hydrocoleum glutinosum var. vermiculare','(Kützing) Gomont 1892','','',NULL,0),(671,'Hydrocoleum glutinosum f. vermiculare','&nbsp;(Kützing) Kossinskaja 1948','','',NULL,0),(672,'Phormidium glutinosum','(Agardh) Braun 1852','','',NULL,0),(673,'Lyngbya glutinosa','Agardh 1824','','',NULL,0),(674,'Hydrocoleum homoeotrichum','Kützing 1843','','pre-starting point',NULL,0),(675,'Hydrocoleum homoeotrichum f. minor','(Voronichin) Elenkin 1949','','',NULL,0),(676,'Hydrocoleum homoeotrichum var. tirolense','Hansgirg 1893','','',NULL,0),(677,'Hydrocoleum homoeotrichum var. calcicola','Hansgirg 1893','','',NULL,0),(678,'Hydrocoleum homoeotrichum var. ecapitata','&nbsp;Wille in Rechinger 1914','','',NULL,0),(679,'Hydrocoleum homoeothrichum var. minus','&nbsp;Geitler 1933','','',NULL,0),(680,'Hydrocoleum homoeothrichum var. tenue','Golubic 1957','','',NULL,0),(681,'Hydrocoleum lyngbyaceum','Kützing 1849','','',NULL,0),(682,'Hydrocoleum lyngbyaceum var. rupestre','Kützing 1849','','',NULL,0),(683,'Hydrocoleum lyngbyaceum var. rupestre','Kützing ex Gomont 1892','','',NULL,0),(684,'Lyngbya olivacea','Zanardini 1839','','',NULL,0),(685,'Phormidium thinoderma','Kützing 1843','','',NULL,0),(686,'Oscillaria littoralis','Desmasiere 1858','','',NULL,0),(687,'Phormidium kuetzingianum','&nbsp;Le Jolis 1863','','',NULL,0),(688,'Microcoleus nigrescens','Ardisone 1872','','',NULL,0),(689,'Hydrocoleus lyngbyaceus','Kützing ex Forti 1907','','',NULL,0),(690,'Hydrocoleum violaceum','Martens 1871','','pre-starting point name',NULL,0),(691,'Hydrocoleum holdenii','Tilden 1901','','',NULL,0),(692,'Hydrocoleum oligotrichum','Braun 1865','','pre-starting point name',NULL,0),(693,'Hydrocoleum ravenelii','Wolle 1877','','pre-starting point name',NULL,0),(694,'Lyngbya scolecoidea','(West &amp; G.S.West) Bourrelly','','',NULL,0),(695,'Pelagothrix clevei','&nbsp;Schmidt 1901','','',NULL,0),(696,'Xanthotrichum contortum','Wille in Schütt 1893, Pflanzenleben d. Hochsee, p. 39','','',NULL,0),(697,'Trichodesmium ehrenbergii','Montagne 1844','','',NULL,0),(698,'Oscillatoria erythraea','(Ehrenberg) Geitler 1932','','',NULL,0),(699,'Trichodesmium hindsii','Montagne 1844','','',NULL,0),(700,'Skujaella erythraea','(Ehrenberg) De Toni 1938','','',NULL,0),(701,'Trichodesmium indicum','(Hauck) Lemmermann 1899','','',NULL,0),(702,'Trichodesmium ehrenbergii f. indicum','&nbsp;Hauck 1888','','',NULL,0),(703,'Oscillatoria hildebrandtii','(Gomont) Geitler 1932','','',NULL,0),(704,'Skujaella hildebrandtii','&nbsp;(Gomont) De Toni 1939','','',NULL,0),(705,'Trichodesmium hildebrandtii f. atlanticum','&nbsp;Reinsch 1904','','',NULL,0),(706,'Oscillatoria hildenbrandtii','&nbsp;(Gomont) Geitler 1932','','',NULL,0),(707,'Planktothrix iwanoffiana','(Nygaard) Umezaki &amp; Watanabe 1994','','',NULL,1),(708,'Oscillatoria iwanoffiana','(Nygaard) Geitler 1932','','',NULL,0),(709,'Oscillatoria iwanoffiana','(Nygaard) Bourrelly &amp; Manguin 1952','','',NULL,0),(710,'Oscillatoria lacustris','(Klebahn) Geitler 1925','','',NULL,0),(711,'Skujaella lacustris','&nbsp;(Klebahn) De Toni 1946','','',NULL,0),(712,'Trichodesmium tenue','Wille 1904','','',NULL,0),(713,'Oscillatoria thiebautii','(Gomont) Geitler 1932','','',NULL,0),(714,'Skujaella thiebautii','(Gomont) De Toni 1939','','',NULL,0),(715,'Trichodesmium thiebautii f. major','Wille','','',NULL,0),(716,'Schizothrix aurantiaca','Kützing 1849','','',NULL,1),(717,'Schizothrix aurantiaca','Kützing ex Gomont 1892','','',NULL,0),(718,'Schizothrix aurantiaca var. crassa','Zeller 1875','','',NULL,0),(719,'Microcoleus aurantiacus','(Kützing) Hansgirg 1887','','',NULL,1),(720,'Microcoleus aurantiacus','(Kützing) Hansgirg ex Hansgirg 1892','','',NULL,1),(721,'Hypheothrix sauteriana','[Grunow in Rabenhorst 1865] ex Hansgirg 1892','','',NULL,0),(722,'Schizothrix grunoviana','Elenkin 1949','','',NULL,0),(723,'Lyngbya sauteriana','(Grunow) Hansgirg 1892','','',NULL,0),(724,'Oscillatoria friesii','Agardh 1817','','',NULL,0),(725,'Schizothrix friesii f. repens','Frémy 1942','','',NULL,0),(726,'Microcoleus friesii','(Agardh) Thuret 1875','','',NULL,0),(727,'Symploca friesii','(Agardh) Rabenhorst 1863','','',NULL,0),(728,'Symploca friesii','(Agardh) Rabenhorst 1863','','',NULL,0),(729,'Schizothrix friesii','[Agardh] ex Gomont 1892','','',NULL,0),(730,'Symploca friesiana','Kützing 1843','','',NULL,0),(731,'Scytonema friesii','(Agardh) Montagne &amp; Fries 1836','','',NULL,0),(732,'Oscillatoria bangii','Carmichael ex Forti 1907','','',NULL,0),(733,'Schizothrix muelleri f. lyngbyoidea','Gomont 1899','','',NULL,0),(734,'Microcoleus muelleri','Gomont 1886','','',NULL,0),(735,'Hypheothrix naegelii','Kützing 1849, Species Algarum, p. 268','','',NULL,1),(736,'Schizothrix naegelii','(Kützing ex Gomont) Geitler 1925','','',NULL,0),(737,'Leibleinia penicillata','Kützing 1847','','',NULL,1),(738,'Heteroleibleinia penicillata','(Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(739,'Symplocastrum penicilatum','(Kutzing) Forti 1907','','',NULL,0),(740,'Schizothrix penicillata','Gomont 1892','','',NULL,1),(741,'Inactis penicillata','(Kützing) Forti 1907','','',NULL,0),(742,'Schizothrix penicillata','Kützing ex Gomont 1892','','',NULL,0),(743,'Lyngbya penicillata','(Kützing) Rabenhorst 1865','','',NULL,0),(744,'Schizothrix purpurascens var. cruenta','Gomont 1892','','',NULL,0),(745,'Schizothrix purpurascens var. fasciculata','&nbsp;Frémy 1924','','',NULL,0),(746,'Schizothrix purpurascens var. pulvinata','Frémy 1924','','',NULL,0),(747,'Schizothrix sauteriana','Grunow ex Forti 1907','','',NULL,1),(748,'Inactis sauteriana','Grunow in Rabenhorst 1865','','',NULL,0),(749,'Inactis sauteriana','Grunow ex Forti 1907','','',NULL,0),(750,'Schizothrix cuspidata var. luteofusca','West &amp; West 1896','','',NULL,0),(751,'Symplocastrum cuspidatum','(West &amp; West) Forti 1907','','',NULL,0),(752,'Symploca laeteviridis','Setchell &amp; Gardner 1903','','',NULL,0),(753,'Schizothrix aurantiaca','Kützing 1849','','',NULL,0),(754,'Microcoleus aurantiacus','(Kützing) Hansgirg 1887','','',NULL,0),(755,'Microcoleus aurantiacus','(Kützing) Hansgirg ex Hansgirg 1892','','',NULL,0),(756,'Schizothrix sauteriana','Grunow ex Geitler 1932','','',NULL,0),(757,'Arthrospira brevis','(Kützing) Drouet 1968','','',NULL,0),(758,'Spirulina curta','(Lemmermann) Geitler 1925, Cyanophycea, p. 344','','',NULL,0),(759,'Spirulina funiformis','(Vouk) de Toni 1946','','',NULL,0),(760,'Spirulina breviarticulata','(Setchell et Gardner) Geitler 1932','','',NULL,0),(761,'Arthrospira fusiformis','&nbsp;(Voronichin) Komárek &amp; Lund 1990','','',NULL,0),(762,'Arthrospira platensis','(Nordstedt) Gomont sensu Rich 1931','','',NULL,0),(763,'Arthrospira platensis f. minor','Rich 1931','','',NULL,0),(764,'Spirulina geitleri f. minor','(Rich) Fott et Karim 1973','','',NULL,0),(765,'Arthrospira fusiformis var. minor','Rich in Iltis 1970','','',NULL,0),(766,'Oscillatoria platensis','(Nordstedt) Bourrelly 1970 p.p.','','',NULL,0),(767,'Arthrospira platensis f. granulata','&nbsp;Desikachary 1959','','',NULL,0),(768,'Spirulina maxima','&nbsp;(Setchell et Gardner) Geitler 1932','','',NULL,0),(769,'Spirulina geitleri','De Toni 1936','','',NULL,0),(770,'Oscillatoria pseudoplatensis','Bourrelly 1970','','',NULL,0),(771,'Oscillatoria gigantea','(Schmidle) Compère 1974','','',NULL,0),(772,'Spirulina gomontiana','(Setchell) Geitler 1925','','',NULL,0),(773,'Spirulina jenneri','(Stizenberger ex Gomont) Geitler 1925','','',NULL,0),(774,'Oscillatoria jenneri','(Gomont) Compère 1974','','',NULL,0),(775,'Oscillatoria laxa','&nbsp;(Smith) Cmpère 1974','[Algues de la région du Lac Tchad. II. Cyanophycées. Série Hydrobiologie 8(3-4): 165-198.]','',NULL,0),(776,'Arthrospira laxa','(Smith) Crow 1927','[The generic characters of Arthrospira and Spirulina Turp.  - Transactions of the American Microscopical Society 46: 142]','',NULL,0),(777,'Raciborskia leopoliensis','&nbsp;(Raciborski) Koczwara 1929','','',NULL,0),(778,'Amalia leopoliensis','(Raciborski) DeToni 1934','','',NULL,0),(779,'Synechococcus leopoliensis','(Raciborski) Komárek 1970','','',NULL,0),(780,'Arthrospira major','(Kützing ex Gomont) Crow 1927','','',NULL,0),(781,'Spirulina oscillarioides','Turpin 1827,','','pre-starting-point syn.',NULL,0),(782,'Spirulina major f. constans','Emoto et Hirose 1952','','',NULL,0),(783,'Oscillatoria oscillarioides','&nbsp;[Turpin] Iltis 1970','','',NULL,0),(784,'Arthrospira major','&nbsp;(Kützing) Chang et Tseng 1990','','',NULL,0),(785,'Spirulina margaritae','(Gomont) Frémy 1927','','',NULL,0),(786,'Arthrospira margaritae','Gomont nom. nud.','','',NULL,0),(787,'Spirulina massartii','(Kufferath) Geitler 1925','','',NULL,0),(788,'Arthrospira massartii var. indica','Desikachary 1959','','',NULL,0),(789,'Spirulina meneghiniana f. fontinalis','Schwabe 1944','','',NULL,0),(790,'Spirulina meneghiniana f. crassa','Bharadwaja 1963','','',NULL,0),(791,'Spirulina meneghiniana f. minor','Hortobágyi 1963','','',NULL,0),(792,'Arthrospira meneghiniana','(Zanardini ex Gomont) Crow 1927','','',NULL,0),(793,'Oscillatoria meneghiniana','Zanardini ex Gomont 1892','','',NULL,0),(794,'Arthrospira miniata var. constricta','Hoffmann','','',NULL,0),(795,'Arthrospira neapolitana','(Kützing ex Gomont) Drouet 1969','','',NULL,0),(796,'Lyngbya brevis','(Kützing ex Gomont) Hansgirg 1892','','',NULL,0),(797,'Oscillatoria brevis var. neapolitana','(Kützing) Gomont 1892','','',NULL,0),(798,'Oscillatoria brevis f. variabilis','Wille 1922','','',NULL,0),(799,'Oscillatoria brevis var. non-granulata','Kamat 1963','','',NULL,0),(800,'Oscillatoria brevis f. acuminata','Claus 1961','','',NULL,0),(801,'Oscillatoria brevis f. capitata','Claus 1961','','',NULL,0),(802,'Oscillatoria neapolitana','Kützing ex Gomont 1892','','',NULL,0),(803,'Oscillatoria terebriformis f. brevis','Kützing ex Schwabe 1944','','',NULL,0),(804,'Oscillatoria brevis','Kützing 1833','','',NULL,0),(805,'Arthrospira nordstedtii','(Gomont) Crow 1927','','',NULL,0),(806,'Spirulina oceanica','(Crouan &amp; Crouan) Crouan &amp; Crouan 1854','','',NULL,0),(807,'Spirulina tenuissima','Kützing 1836','','',NULL,0),(808,'Oscillatoria oceanica','Crouan 1852','','',NULL,0),(809,'Spirulina subsalsa f. genuina','Gomont 1892','','',NULL,0),(810,'Spirulina subsalsa f. oceanica','(Crouan) Gomont 1892','','',NULL,0),(811,'Spirulina neumannii','Schmidle 1901','','',NULL,0),(812,'Spirulina compacta','Perfilev 1923','','',NULL,0),(813,'Spirulina tenuissima var. salina','Wisłouch 1924','','',NULL,0),(814,'Spirulina supersalsa','Schiller 1956','','',NULL,0),(815,'Spirulina condesata','Welsh 1964','','',NULL,0),(816,'Oscillatoria subsalsa','(Oersted) Bourrelly 1970','','',NULL,0),(817,'Oscillatoria neumannii','(Schmidle) Iltis 1972','','',NULL,0),(818,'Arthrospira oceanica','Crow 1927','','',NULL,0),(819,'Arthrospira tenuissima','(Kützing) Crow 1927','','',NULL,0),(820,'Arthrospira subsalsa','(Oersted ex Gomont) Crow 1927','','',NULL,0),(821,'Oscillatoria subsalsa','Agardh 1824','','',NULL,0),(822,'Lyngbya subsalsa','(Agardh) Hansgirg 1893','','',NULL,0),(823,'Spirulina okensis','(Meyer) Geitler 1932','','',NULL,0),(824,'Spirulina platensis','(Gomont) Geitler 1925','','',NULL,0),(825,'Spirulina platensis var. tenuis','Rao 1937','','',NULL,0),(826,'Spirulina platensis var. non-constricta','Banerji 1938','','',NULL,0),(827,'Oscillatoria platensis','(Nordstedt) Bourrelly 1970 p.p.','','',NULL,0),(828,'Arthrospira platensis var. tenuis','(Rao) Desikachary 1959','','',NULL,0),(829,'Hydrocoleum platense','Nordstedt in Wittrock &amp; Nordstedt 1889','','',NULL,0),(830,'Spirulina setchellii','De Toni 1937','','',NULL,0),(831,'Spirulina gigantea','SCHMIDLE sensu SKUJA (1949)','','',NULL,0),(832,'Spirulina spirulinoides f. tenuis','Singh 1939','','',NULL,0),(833,'Spirulina spirulinoides f. tenuis','Singh 1939','','',NULL,1),(834,'Arthrospira spirulinoides f. tenuis (','Singh) Desikachary 1959','','',NULL,0),(835,'Oscillatoria spirulinoides','Woronichin 1932','','',NULL,0),(836,'Arthrospira subtilissima','(Kützing) Crow 1927','','',NULL,0),(837,'Spirulina subtilissima var. brevis','Croasdale 1948','','',NULL,0),(838,'Spirulina subtilissima','Kützing 1843','','pre-starting point name',NULL,0),(839,'Spirulina tenuis','(Brühl &amp; Biswas) Geitler 1925','','',NULL,0),(840,'Arthrospira platensis var. tenuis','(Rao) Desikachary 1959','','',NULL,0),(841,'Spirulina tenuissima f. versicolor','Kosinskaja 1948','','',NULL,0),(842,'Spirulina subsalsa f. versicolor','Koster 1958','','',NULL,0),(843,'Spirulina subsalsa status versicolor','Anagnostidis et Golubić 1966','','',NULL,0),(844,'Arthrospira versicolor','(Cohn ex Gomont) Crow 1927','','',NULL,0),(845,'Oscillaria microcoleiformis','Crouan 1867','','pre-starting point name',NULL,0),(846,'Hypheothrix acutissima','Gardner 1927','','',NULL,0),(847,'Microcoleus acutissimus var. colorata','Bongale 1987','','',NULL,0),(848,'Microcoleus acutissimus f. minor','Bongale 1987','','',NULL,0),(849,'Phormidium amoenum','Kützing ex Gomont 1892','','',NULL,0),(850,'Phormidium amoenum','Kützing 1843','','',NULL,0),(851,'Phormidium amoenum','Kützing ex Anagnostidis &amp; Komárek 1988','','',NULL,0),(852,'Phormidium amoenum var. infusionum','Kützing ex Elenkin 1949','','',NULL,0),(853,'Oscillatoria amoena f. maharastrensis','Kamat 1963','','',NULL,0),(854,'Oscillatoria amoena var. major','Vasishta 1965','','',NULL,0),(855,'Oscillatoria amoena var. lacustris','Margalef 1952','','',NULL,0),(856,'Oscillatoria amoena var. non-granulata','Ghose 1927','','',NULL,0),(857,'Lyngbya amoena','Hansgirg 1892','','',NULL,0),(858,'Lyngbya boryana','Kirchner ex Hansgirg 1892','','',NULL,0),(859,'Microcoleus boryanus','(Kützing) Rabenhorst 1847','','',NULL,0),(860,'Dasygloea amorpha','Thwaites 1848','','',NULL,0),(861,'Microcoleus amorphous','Wolle 1887','','',NULL,0),(862,'Microcoleus amplus var. minor','Kamat 1963','','',NULL,0),(863,'Microcoleus anguiformis','Harvey in Hassall 1845','','',NULL,0),(864,'Phormidium attenuatum','(Fritsch) Anagnostidis &amp; Komárek 1988','','',NULL,0),(865,'Phormidium autumnale','Trevisan 1844','','',NULL,0),(866,'Oscillatoria autumnalis','Agardh 1812','','',NULL,0),(867,'Lyngbya antliaria','(Mertens) Hansgirg 1885','','',NULL,0),(868,'Lyngbya antliaria var. repens','(Agardh) Kirchner ex Hansgirg 1892','','',NULL,0),(869,'Lyngbya autumnalis','(Gomont) Senna 1983','','',NULL,0),(870,'Oscillatoria antliaria','Mertens in Jürgens 1822','','',NULL,0),(871,'Phormidium antliarium','(Mertens) Gomont 1890','','',NULL,0),(872,'Oscillatoria beggiatoiformis','Rabenhorst 1865','','',NULL,0),(873,'Phormidium beggiatoiforme','(Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(874,'Oscillatoria terebriformis f. beggiatoiformis','Elenkin 1949','','',NULL,0),(875,'Oscillatoria terebriformis var. beggiatoiformis','Grunow in Rabenhorst 1865','','',NULL,0),(876,'Phormidium biasolettianum','Kützing 1843','','',NULL,0),(877,'Microcoleus biasolettianus','(Kützing) Rabenhorst 1847','','',NULL,0),(878,'Phormidium papyraceum var. biasolettianum','(Kützing) Dalla Torre &amp; Sarnthein 1901','','',NULL,0),(879,'Lyngbya membranacea var. biasolettiana','(Kützing) Hansgirg ex Forti 1907','','',NULL,0),(880,'Hydrocoleum brebissonii','Kützing 1845-1849','','',NULL,0),(881,'Microcoleus brebissonii var. aerugineus','Rabenhorst ex Hansgirg 1892','','',NULL,0),(882,'Chthonoblastus burmanicus','Zeller 1873','','',NULL,0),(883,'Phormidium calidum','Gomont 1890','','',NULL,0),(884,'Phormidium calidum var. olivaceum','Gardner 1927','','',NULL,0),(885,'Oscillatoria tenuis var. calida','(Agardh) Mougéot &amp; Rouméguère 1887','','',NULL,0),(886,'Lyngbya calida','Borge 1933','','',NULL,0),(887,'Oscillatoria calida','Agardh in Kunth 1822','','',NULL,0),(888,'Microcoleus cataractarum','Hansgirg 1890','','',NULL,0),(889,'Phormidium caucasicum','(Elenkin &amp; Kossinskaja) Anagnostidis 2001','','',NULL,0),(890,'Conferva chthonoplastes','Mertens in Hornemann 1813','','',NULL,0),(891,'Oscillatoria chtonoplastes','Hofman-Bang ex Gomont 1892','','',NULL,0),(892,'Microcoleus chthonoplastes var. lyngbyei','(Kützing) Rabenhorst in Hansgirg 1893','','',NULL,0),(893,'Oscillatoria corium','Agardh 1812','','',NULL,0),(894,'Microcoleus corium','(Agardh) Rabenhorst 1847','','',NULL,0),(895,'Phormidium corium f. terrestre','Mitra 1951','','',NULL,0),(896,'Phormidium corium var. constrictum','Playfair 1915','','',NULL,0),(897,'Phormidium corium','(Agardh) Kützing 1843','','',NULL,0),(898,'Lyngbya corium','Hansgirg 1892','','',NULL,0),(899,'Microcoleus corymbosus','Harvey 1858','','',NULL,0),(900,'Polythrix corymbosa','[Harvey] Grunow ex Bornet et Flahault 1886','','',NULL,0),(901,'Microcoleus curvatus','Meneghini 1842','','',NULL,0),(902,'Lyngbya curvata f. viridis','Rabenhorst 1865 ex Gomont 1892','','',NULL,0),(903,'Scytonema curvatum','(Meneghini) Borzì 1879','','',NULL,0),(904,'Siphoderma curvatum','(Meneghini) Kützing 1843','','',NULL,0),(905,'Chthonoblastus burmanicus','Zeller 1873','','',NULL,0),(906,'Lyngbya favosa','(Gomont) Thérézien &amp; Couté 1977','','',NULL,0),(907,'Oscillatoria favosa','Bory 1827','','',NULL,0),(908,'Sirocoleum guyanense','Gomont 1890','','',NULL,0),(909,'Microcoleus guyanensis','Gomont ex Gomont 1892','','',NULL,0),(910,'Phormidium hiemale','(Jaag) Anagnostidis 2001','','',NULL,0),(911,'Microcoleus hospitus','Hansgirg 1890','','',NULL,0),(912,'Microcoleus hospitus','Hansgirg ex Forti 1907','','',NULL,0),(913,'Microcoleus hospita var. elongatus','Nygaard 1932','','',NULL,0),(914,'Microcoleus hospita var. epilithicus','Ercegovic 1925','','',NULL,0),(915,'Schizothrix hyaline','Kützing 1849','','',NULL,0),(916,'Microcoleus irriguus','(Kützing) Drouet 1968','','',NULL,0),(917,'Phormidium irriguum f. minor','Sciuto &amp; Moro 2012','','',NULL,0),(918,'Microcoleus lacustris f. minor','Desikachary 1959','','',NULL,0),(919,'Microcoleus lacustris f. intermedius','Vasishta 1961','','',NULL,0),(920,'Phormidium leptodermum','Kützing 1843','','',NULL,0),(921,'Phormidium leptodermum','Kützing ex Forti 1907','','',NULL,0),(922,'Phormidium leptodermum var. capitatum','Gardner 1927','','',NULL,0),(923,'Lyngbya leptoderma','(Kützing) Kirchner 1880','','',NULL,0),(924,'Phormidium vulgare var. leptodermum','Kützing 1849','','',NULL,0),(925,'Lyngbya vulgaris var. leptoderma','Kützing ex Hansgirg 1892','','',NULL,0),(926,'Calothrix limbata','Harvey 1863','','',NULL,0),(927,'Oscillatoria tenuis var. limicola','(Kützing) Anzi 1875','','',NULL,0),(928,'Microcoleus lucidus','(Agardh) Rabenhorst 1847','','',NULL,0),(929,'Lyngbya lucida','(Kützing ex Gomont) Hansgirg 1892','','',NULL,0),(930,'Oscillatoria lucida','Agardh 1827','','',NULL,0),(931,'Phormidium lyngbyaceum','Kützing 1843','','',NULL,0),(932,'Microcoleus lyngbyaceum','Kützing 1849','','',NULL,0),(933,'Lyngbya lyngbyacea','(Kützing) Hansgirg 1884','','',NULL,0),(934,'Microcoleus lyngbyaceus var. vermiformis','Baker et Bold 1970','','',NULL,0),(935,'Chthonoplastus lyngbyei','Kützing 1843','','',NULL,0),(936,'Oscillatoria lyngbyacea','Kützing 1843','','',NULL,1),(937,'Chthonoblastus paludosus','Kützing 1849','','',NULL,0),(938,'Microcoleus paludosus f. granulosus','(Degterev) Poljanskij 1953','','',NULL,0),(939,'Microcoleus paludosus var. acuminatus','Gardner 1927','','',NULL,0),(940,'Microcoleus pannosus','(Bory) Rabenhorst 1847','','',NULL,0),(941,'Phormidium pannosum','(Bory) Kützing 1843 ex Gomont 1892','','',NULL,0),(942,'Oscillatoria pannosa','Bory 1827','','',NULL,0),(943,'Chthonoblastus plantae','Brügger 1863','','',NULL,0),(944,'Microcoleus polythrix','Hansgirg ex Gomont 1892','','',NULL,0),(945,'Inactis polythrix','Forti 1907','','',NULL,0),(946,'Microcoleus pulvinatus','Wolle ex Gomont 1892','','',NULL,0),(947,'Microcoleus repens','(Agardh) Harvey 1841','','',NULL,0),(948,'Oscillatoria repens','Agardh 1824','','',NULL,0),(949,'Oscillatoria retzii','Agardh 1812','','',NULL,0),(950,'Microcoleus retzii','(Agardh) Rabenhorst 1847','','',NULL,0),(951,'Phormidium retzii f. majus','Parukutty 1940','','',NULL,0),(952,'Phormidium retzii f. fasciculata','Gomont 1892','','',NULL,0),(953,'Phormidium retzii f. rupestris','Gomont 1892','','',NULL,0),(954,'Lyngbya retzii','Hansgirg 1892','','',NULL,0),(955,'Oscillatoria rupestris','Agardh 1824','','',NULL,0),(956,'Microcoleus rupestris','(Agardh) Rabenhorst 1847','','',NULL,0),(957,'Lyngbya rupestris var. rivularis','Kützing ex Hansgirg 1892','','',NULL,0),(958,'Phormidium rupestre','(Agardh) Kützing 1849','','',NULL,0),(959,'Phormidium rupestre var. rivulare','Kützing ex Elenkin 1949','','',NULL,0),(960,'Oscillatoria rupestris','Agardh 1824 ex Gomont 1892','','',NULL,0),(961,'Microcoleus rupicola','(Tilden) Drouet 1943','[Field Museum of Natural History][ Botanical Series 20: 145-176]','',NULL,0),(962,'Lyngbya setcheliana','(Gomont) Bourrelly 1984','','',NULL,0),(963,'Microcoleus sociatus var. tenuis','Behre 1953','','',NULL,0),(964,'Lyngbya subtorulosa','(Brébisson) Kirchner ex Hansgirg 1892','','',NULL,0),(965,'Microcoleus subtorulosus var. rupestris','Li 1989','','',NULL,0),(966,'Phormidium subtorulosum','Brébisson in Kützing 1847','','',NULL,0),(967,'Oscillatoria subtorulosa','(Brébisson) Farlow ex Forti 1907','','',NULL,0),(968,'Lyngbya subtorulosa','(Brébisson) Hauck ex Hansgirg 1892','','',NULL,0),(969,'Lyngbya subtorulosa','(Gomont ex Gomont) Hansgirg 1893','','',NULL,0),(970,'Schizothrix tenerrima','(Gomont) Drouet 1968','','',NULL,0),(971,'Microcoleus tenerrimus var. minor','Elenkin 1949','','',NULL,0),(972,'Microcoleus tenerrimus var. longus','Umezaki 1952','','',NULL,0),(973,'Microcoleus terrestris var. vaucheri','(Kützing) ex Kirchner ex Hansgirg 1892','','',NULL,0),(974,'Microcoleus terrestris var. repens','(Kützing) ex Kirchner ex Hansgirg 1892','','',NULL,0),(975,'Microcoleus thinoderma','(Kützing) Rabenhorst 1847','','',NULL,0),(976,'Microcoleus lyngbyaceus','Thuret 1875','','',NULL,0),(977,'Microcoleus lyngbyaceus','Thuret ex Gomont 1892','','',NULL,0),(978,'Oscillatoria vaginata','Vaucher 1803','','',NULL,0),(979,'Trichophorus vaginatus','(Vaucher) Desvaux 1809','','',NULL,0),(980,'Microcoleus vaginatus var. vaucheri','Gomont 1892','','',NULL,0),(981,'Microcoleus vaginatus var. monticola','Gomont 1892','','',NULL,0),(982,'Microcoleus annulatus','Fritsch et Rich 1924','','',NULL,1),(983,'Microcoleus vaginatus f. annulatus','Geitler ex Elenkin 1949','','',NULL,0),(984,'Geitlerinema sandbergii','(Skuja) Anagnostidis 2001','','',NULL,0),(985,'Oscillatoria sandbergii','Skuja 1964','','',NULL,0),(986,'Microcoleus vaginatus f. monticola','(Gomont) Elenkin in Starmach 1973','','',NULL,0),(987,'Microcoleus vaginatus var. acuminatus','Gardner 1927','','',NULL,0),(988,'Microcoleus vaginatus var. minor','Gardner 1927','','',NULL,0),(989,'Conferva vaginata','(Vaucher) Sprengel 1806','','',NULL,0),(990,'Microcoleus vermicularis','Hauck 1885','','',NULL,0),(991,'Hydrocoleum glutinosum var. vermiculare','Gomont 1892','','',NULL,1),(992,'Lyngbya vermicularis','Rabenhorst 1865','','',NULL,0),(993,'Phormidium vulgare','Kützing ex Gomont 1892','','',NULL,0),(994,'Phormidium vulgare var. luteum','[Agardh] Kützing ex Elenkin 1949','','',NULL,0),(995,'Phormidium vulgare var. myochroum','Kützing ex Elenkin 1949','','',NULL,0),(996,'Lyngbya vulgaris','Kirchner ex Hansgirg 1892','','',NULL,0),(997,'Lyngbya vulgaris var. lutea','Kützing ex Hansgirg 1892','','',NULL,0),(998,'Lyngbya vulgaris var. myochroa','Kützing ex Hansgirg 1892','','',NULL,0),(999,'Lyngbya vulgaris var. purpurascens','Kützing ex Hansgirg 1892','','',NULL,0),(1000,'Lyngbya vulgaris var. fusca','Kützing ex Hansgirg 1892','','',NULL,0),(1001,'Lyngbya vulgaris var. leptoderma','Hansgirg ex Forti 1907','','',NULL,0),(1002,'Oscillaria vulgaris','(Kützing) P.Crouan &amp; H.Crouan 1867','','',NULL,0),(1003,'Oscillatoria violacea','Wallroth 1833','','',NULL,0),(1004,'Phormidium violaceum','(Wallroth ex Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(1005,'Lyngbya violacea','(Wallroth) Hansgirg 1892','','',NULL,0),(1006,'Schizothrix furcata','Rabenhorst 1865','','',NULL,1),(1007,'Microcoleus heterotrichus','[Kützing] Wolle ex Hansgirg 1892','','',NULL,0),(1008,'Hydrocoleum heterotrichum','Kützing 1843','','',NULL,0),(1009,'Vaginaria racomitrii','Kützing 1836','','',NULL,0),(1010,'Inactis heterotrichum','Kirchner 1878','','',NULL,0),(1011,'Microcoleus heterotrichus','Wolle 1887','','',NULL,0),(1012,'Hydrocoleum heterotrichum','Gomont 1890','','',NULL,0),(1013,'Schizothrix furcata','Rabenhorst 1865','','',NULL,0),(1014,'Phormidium lyngbyaceum','Kützing ex Gomont 1892','','',NULL,0),(1015,'Chthonoblastus salinus','Kützing 1843','','',NULL,0),(1016,'Microcoleus gracilis var. salinus','Kützing ex Wolle 1887','','',NULL,0),(1017,'Oscillatoria agardhii f. aequicrassa','Elenkin 1949','','',NULL,0),(1018,'Oscillatoria agardhii f. moebiusii','Elenkin 1949','','',NULL,0),(1019,'Oscillatoria agardhii f. lemmermannii','Elenkin 1949','','',NULL,0),(1020,'Oscillatoria agardhii f. wislouchii','Elenkin 1949','','',NULL,0),(1021,'Oscillatoria agardhii f. gomontii','Elenkin 1949','','',NULL,0),(1022,'Oscillatoria compressa','(Utermöhl) Geitler 1925','','',NULL,0),(1023,'Oscillatoria (Oscillaria) geitleri','Kiselev 1927 ex Elenkin 1949','','',NULL,0),(1024,'Oscillatoria agardhii f. isothrix','(Skuja) Poljansky 1953','','',NULL,0),(1025,'Oscillatoria mougeotii','Kützing ex Forti 1907','','',NULL,0),(1026,'Oscillatoria mougeotii f. clathrata','Skuja ex Starmach 1966','','',NULL,0),(1027,'Planktothrix mougeotii','(Bory ex Gomont) Anagnostidis et Komárek 1988 sine typo','','',NULL,0),(1028,'Oscillatoria mougeotii var. major','Elenkin 1914','','',NULL,0),(1029,'Oscillatoria mougeotii f. major','(Elenkin) Elenkin 1949','','',NULL,0),(1030,'Oscillatoria perornata f. attenuata','Skuja 1949','','',NULL,0),(1031,'Planktothrix perornata','(Skuja) Anagnostidis et Komárek 1988','','',NULL,0),(1032,'Lyngbya prolifica','Greville 1828','','',NULL,0),(1033,'Oscillatoria rubescens var. caucasica','Schmidle 1897','','',NULL,0),(1034,'Oscillatoria rubescens f. caucasica','(Schmidle) Elenkin 1949','','',NULL,0),(1035,'Oscillatoria rubescens var. crassior','Kützing ex Gomont 1892','','',NULL,0),(1036,'Oscillatoria rubescens f. crassior','Kützing ex Forti 1907','','',NULL,0),(1037,'Oscillatoria rubescens var. curvata Kamat 1963','Kamat 1963','','',NULL,0),(1038,'Oscillatoria rubescens var. kolhapurensis','Kamat 1963','','',NULL,0),(1039,'Oscillatoria rubescens f. varesensis','Grunow ex Forti 1907','','',NULL,0),(1040,'Oscillatoria pharaonis','Bory 1827','','',NULL,0),(1041,'Oscillatoria pharaonis','Bory ex Gomont 1892','','',NULL,0),(1042,'Pseudophormidium edaphicum','(Elenkin) Anagnostidis &amp; Komárek 1988','','',NULL,0),(1043,'Leptolyngbya battersii','(Gomont) Anagnostidis &amp; Komárek 1988','','',NULL,0),(1044,'Plectonema edaphicum','(Elenkin) Vaulina 1959','','',NULL,0),(1045,'Placoma','Schousboe ex Bornet et Thuret, 1876. Notes Algol. 1: 4.','','',268,1),(1046,'Placoma vesiculosum','Schousboe ex Bornet et Thuret 1876','','',1562,1),(1047,'Placoma regulare','Broady et Ingerfeld 1991. Phycologia 30(6): 548','[532]',NULL,2200,1),(1048,'Placoma adriatica','Hauck 1885','','',NULL,1),(1049,'Oncobyrsa adriatica','(Hauck) Molinari et Guiry 2021. Notulae algarum 183: 2','undefined',NULL,2485,0),(1050,'Placoma','Molinari et Guiry 2021. Notulae algarum 183: 2','',NULL,2487,0),(1051,'Placoma adriatica','Hauck 1895. Kryptogamen-Flora von Deutschland, Österreich und der Schweiz. Zweite Auflage: 515','null',NULL,2485,0),(1052,'Placoma regulare','Broady et Ingerfeld 1991. Phycologia 30(6): 548','[532]',NULL,2491,0),(1053,'Placoma vesiculosa','Schousboe ex Bornet et Thuret 1876','null',NULL,2488,0),(1054,'Placoma willei','(Gardner) Molinari et Guiry 2021. Notulae Algarum 183: 3','[215]',NULL,2493,0),(1055,'Placoma violacea','(Setchell et N.L.Gardner) Molinari et Guiry 2021. Notulae Algarum 183: 3','undefined',NULL,2492,0),(1056,'Oncobyrsa adriatica var. micrococca','(Hansgirg) Molinari et Guiry 2021. Notulae Algarum 183: 2','null',NULL,2490,0),(1057,'Oncobyrsa africana','(Wille) Molinari et Guiry 2021. Notulae Algarum 183: 2','null',NULL,2489,0),(1058,'Ophiothrix','Molinari et Guiry 2021. Notulae Algarum 183: 2','[52]',NULL,698,0),(1059,'Ophiothrix epidendron','Sant Anna, Azevedo, Kaštovský et Komárek, 2010, Fottea 10(2): 218','[52]',NULL,771,0),(1060,'Ophiothrix epibryos','(Komárek) Sant Anna, Azevedo, Kaštovský et Komárek 2010, Fottea 10(2): 220','',NULL,772,0),(1061,'Ophiothrix hansgirgii','(Schmidle) Sant Anna, Azevedo, Kaštovský et Komárek 2010, Fottea 10(2): 220','',NULL,773,0);
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