| Generic name: CYANOCYSTIS Borzi, 1882. Nuovo Giorn. Bot. Ital. 14: 314.
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Synonyms:
SPHAENOSIPHON Reinsch, 1874/1875. Contr. alg. fung., p. 15.
KRKIA Pevalek 1929
DERMOCARPA Crouan p. p. excl. typo (incl. sensu Waterbury & Stanier 1978
p.p.)
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| Diagnosis:
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| Type species: Cyanocystis versicolor Borzi 1882. |
Descriptions:
Komárek & Anagnostidis (1998): 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 (1992): 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
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| Genotype differences, molecular data:
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Reproduction strategies, life cycles, cell division:
Komárek & Anagnostidis (1998): 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 (1992): 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
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| Ultrastructure:
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Taxonomic position, higher hierarchy:
Cyanophyceae, Chroococcales, Dermocarpellaceae
Notes to taxonomy, misinterpretations:About 16 species
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Ecology, ecophysiology, ecological significance:
Komárek (1992): 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.
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Physiology and biochemistry:
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Distribution, endemism, problematic citations:
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Reference strain:
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Infrageneric scheme, species concept:
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List of species:
Cyanocystis aquae-dulcis (Reinsch) Kann 1978
Cyanosystis croatica (Pevalek) Komárek et Anagnostidis 1995
Cyanocystis farlowii (Börgesen) Komárek et Anagnostidis 1986
Cyanocystis flahaultii (Sauvageau) Komárek et Anagnostidis 1995
Cyanocystis hemisphaerica (Setchel et Gardner) Kaas 1985
Cyanocystis mexicana Montejano et al. 1993
Cyanocystis minima (Geilter) Komárek et Anagnostidis 1986
Cyanocystis olivacea (Reinsch) Komárek et Anagnostidis 1986
Cyanocystis pacifica (Setchell et Gardner) Komárek et Anagnostidis 1986
Cyanocystis plectonematis (Frémy) Komárek et Anagnostidis 1986
Cyanocystis pseudoxenococcoides (Bourrelly) Bourrelly 1970
Cyanocystis sphaeroidea (Setchell et Gardner) Komárek et Anagnostidis 1986
Cyanocystis tatrensis (Starmach) Komárek et Anagnostidis 1995
Cyanocystis valie-allorgei (Bourrelly) Bourrelly 1970
Cyanocystis versicolor Borzi 1882
Cyanocystis violacea (Crouan) Komárek et Anagnostidis 1986
Cyanocystis xenococcoides (Geitler) Compere 1985
Unclear taxa:
Cyanocystis parva Conrad 1914
Dermocarpa bicayensis Sauvageau 1895
Dermocarpa cavanillesiana Gonzalez-Guerrero 1946
Dermocarpa cuspidata (Reinsch) Geitler 1932
Dermocarpa depressa W. et G.S. West 1897
Dermocarpa elliptica Skovotzov 1946
Dermocarpa enteromorphae Anand 1937
Dermocarpa fossae Fjerdingstad 1950
Dermocarpa gaditana Gonzalez 1947
Dermocarpa gardneriana Drouet 1942
Dermocarpa hollenbergii Drouet 1942
Dermocarpa marchantae Setchell et Gardnet 1924
Dermocarpa minuta Drouet 1942
Dermocarpa reinschii Setchell et Gardner 1924
Dermocarpa rosea (Reinsch) Batters 1889
Dermocarpa setchelli Drouet 1942
Dermocarpa smaragdina (Reinsch) Tilden 1910
Dermocarpa solheimii Drouet 1942
Dermocarpa sorediformis (Reinsch) Geitler 1932
Dermocarpa strangulata Sauvageau 1895
Dermocarpa vickersiae Collins 1911
Dermocarpa xenococcoides f. minor Geitler in Geilter et Ruttner 1935
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| Keys:
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| List of stains: |
Drawings:
Komárek (1992)
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| Application technology:
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Literature:
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2.1 taxonomy: Geitler 1932(sub Dermocarpa), Feldmann & Feldmann 1953, Ginsburg-Ardre 1966, Geitler 1967, Ardre 1969, Bourrelly 1970, Geitler 1975, Bourrelly 1977, Christensen 1980, Kaas 1985, Bourrelly 1985, Komárek & Anagnostidis 1986, Friedmann & Friedmann 1989, Hua & al. 1989, Komárek 1992, Komárek & Anagnostidis 1998 |
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2.2 cytomorphology:
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2.3 16S rRNA sequencing:
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2.4 biology and life cycles:
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2.5 ecology:
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