Rma. Velzeboer et al., Geographical patterns of occurrence and composition of saxitoxins in the cyanobacterial genus Anabaena (Nostocales, Cyanophyta) in Australia, PHYCOLOGIA, 39(5), 2000, pp. 395-407
Cyanobacterial samples were collected between April 1989 and May 1997 from
six drainage divisions in coastal areas of Australia: the northeast coast,
southeast coast, Tasmania, Murray-Darling Basin, South Australian coast and
southwest coast. Saxitoxins were detected in approximately 70% of all fiel
d samples and 57% of cultured strains of Anabaena circinalis. Maximum saxit
oxin concentrations were 4466 and 2553 mug g(-1) dry weight cells in field
samples and strains, respectively. Toxin profiles were similar in the major
ity of field samples and strains. The toxins were predominantly C-toxins (C
1 and C2) and gonyautoxins (GTX2 and GTX3), with saxitoxin sensu stricto (S
TX). GTX5 and decarbamoyl gonyautoxins (dcGTX2 and dcGTX3) being present in
minor amounts, A unique toxin composition (exclusively STX and GTX5) was F
ound in a geographically isolated strain from the southwest coast of Austra
lia. N1-hydroxy saxitoxins (neoSTX, GTX1 and GTX4) were not detected in any
field sample or cultured strain. Anabaena circinalis may not be the only A
nabaena species producing saxitoxins, as very low concentrations of GTX3 (1
4 mug g(-1) dry weight cells or less) were detected in two other Anabaena s
pecies: A. perturbata var. tumida and A. spiroides. One decarbamoyl gonyaut
oxin (dcGTX3) was also present in one A. perturbata var. tumida strain. Ana
toxin-a was not detected in Australian strains of Anabaena. Trace amounts o
f 0.23 and 0.10 mug microcystin-LR equivalents g(-1) dry weight cells were
found in two cultured strains of Anabaena cylindrica. An increase in toxin
concentration from 0 to 4423 mug saxitoxins gl dry weight cells was observe
d over a 3-month period in a series of samples collected from a persistent
bloom of A. circinalis at Wongulla Lagoon. South Australia. This temporal v
ariation in saxitoxin concentrations is similar to that reported for microc
ystins in Microcystis aeruginosa (Chroococcales, Cyanophyta).