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(A and B) Arthronema gygaxiana UTCC393, showing involution cell (A) and asymmetric cell division (B). (C and D) Pseudanabaena tremula UTCC471, showing typical unconstricted trichomes without sheaths (C) as well as rare subtly constricted trichomes with sheaths (D). (E-H) Leptolyngbya angustata UTCC 473, showing false branching (E), hormogonia (F), tapered hormogonium (G), and multiple trichomes in a common sheath (H). (I) Leptolyngbya tenerrima. Scale bars, 10 mm.

(A and B) Arthronema gygaxiana UTCC393, showing involution cell (A) and asymmetric cell division (B). (C and D) Pseudanabaena tremula UTCC471, showing typical unconstricted trichomes without sheaths (C) as well as rare subtly constricted trichomes with sheaths (D). (E-H) Leptolyngbya angustata UTCC 473, showing false branching (E), hormogonia (F), tapered hormogonium (G), and multiple trichomes in a common sheath (H). (I) Leptolyngbya tenerrima. Scale bars, 10 mm.

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... The 50 μL PCR reaction contained: 27 μL DNA containing supernatant, 0.5 μL of each primer (0.01 mM concentration), and 22 μL PCR Master Mix (Promega, Madison, WI, USA). PCR amplification proceeded as detailed in Casamatta et al. (2005), and products were frozen and sent to Eurofins Scientific (Louisville, Kentucky) for Sanger sequencing. ...
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