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JPR Advance Access originally published online on April 27, 2004
Journal of Plankton Research 2004 26(8):925-935; doi:10.1093/plankt/fbh084
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Journal of Plankton Research Vol. 26 No. 8 © Oxford University Press 2004; all rights reserved

Cyanobacteria and cyanobacterial toxins in three alkaline Rift Valley lakes of Kenya—Lakes Bogoria, Nakuru and Elmenteita

Andreas Ballot*, Lothar Krienitz, Kiplagat Kotut1, Claudia Wiegand2, James S. Metcalf3, Geoffrey A. Codd3 and Stephan Pflugmacher2

Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Department of Limnology of Stratified Lakes, Alte Fischerhütte 2, D-16775 Stechlin, Germany, 1 Kenyatta University, Botany Department, Po Box 43844, Nairobi, Kenya, 2 Leibniz-Institute of Freshwater Ecology and Inland Fisheries, AG Biogeochemical Regulation, Müggelseedamm 301, D-12587 Berlin, Germany and 3 Division of Environmental and Applied Biology, School of Life Sciences, University of Dundee, Dundee DD1 4HN, UK

* Corresponding Author: ballot{at}igb-berlin.de

Received December 17, 2003; accepted in principle February 11, 2004; accepted for publication April 13, 2004; published online April 27, 2004

For decades frequent mass mortalities of Lesser Flamingos (Phoeniconaias minor Geoffroy) have been observed at alkaline-saline Kenyan Rift Valley lakes. To estimate the potential influence of toxic cyanobacteria on these mass deaths, the phytoplankton communities were investigated in Lakes Bogoria, Nakuru and Elmenteita. Cyanobacterial toxins were analyzed both in the phytoplankton from the three lakes and in isolated monocyanobacterial strains of Arthrospira fusiformis, Anabaenopsis abijatae, Spirulina subsalsa and Phormidium terebriformis. Lake Bogoria was dominated by the cyanobacterium A. fusiformis. In L. Nakuru and L. Elmenteita the phytoplankton mainly consisted of A. fusiformis, A. abijatae and Anabaenopsis arnoldii, and in L. Nakuru an unknown Anabaena sp. was also found. Furthermore, this is the first time A. abijatae and the unknown Anabaena sp. have been found in Kenyan lakes. Phytoplankton wet weight biomass was found to be high, reaching 777 mg L–1 in L. Bogoria, 104 mg L–1 in L. Nakuru and 202 mg L–1 in L. Elmenteita. Using HPLC, the cyanobacterial hepatotoxins microcystin-LR, -RR -YR, -LF and -LA and the neurotoxin anatoxin-a were detected in phytoplankton samples from L. Bogoria and L. Nakuru. Total microcystin concentrations amounted to 155 µg microcystin-LR equivalents g–1 DW in L. Bogoria, and 4593 µg microcystin-LR equivalents g–1 DW in L. Nakuru, with anatoxin-a concentrations at 9 µg g–1 DW in L. Bogoria and 223 µg g–1 DW in L. Nakuru. In L. Elmenteita phytoplankton, no cyanobacterial toxins were found. A. fusiformis was identified as one source of the toxins. The isolated strain of A. fusiformis from L. Bogoria was found to produce both microcystin-YR (15.0 µg g–1 DW) and anatoxin-a (10.4 µg g–1 DW), whilst the A. fusiformis strain from L. Nakuru was found to produce anatoxin-a (0.14 µg g–1 DW). Since A. fusiformis mass developments are characteristic of alkaline-saline lakes, health risks to wildlife, especially the Arthrospira-consuming Lesser Flamingo, may be expected.


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