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Species-dependent variation in sensitivity of Microcystis species to copper sulfate: implication in algal toxicity of copper and controls of blooms
Copper sulfate is a frequently used reagent for Microcystis blooms control but almost all the previous works have used Microcystis aeruginosa as the target organism to determine dosages. The aim of this study was to evaluate interspecific differences in the responses of various Microcystis species t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227962/ https://www.ncbi.nlm.nih.gov/pubmed/28079177 http://dx.doi.org/10.1038/srep40393 |
Sumario: | Copper sulfate is a frequently used reagent for Microcystis blooms control but almost all the previous works have used Microcystis aeruginosa as the target organism to determine dosages. The aim of this study was to evaluate interspecific differences in the responses of various Microcystis species to varying Cu(2+) concentrations (0, 0.05, 0.10, 0.25, and 0.50 mg L(−1)). The half maximal effective concentration values for M. aeruginosa, M. wesenbergii, M. flos-aquae, and M. viridis were 0.16, 0.09, 0.49, and 0.45 mg L(−1) Cu(2+), respectively. This showed a species-dependent variation in the sensitivity of Microcystis species to copper sulfate. Malonaldehyde content did not decrease with increasing superoxide dismutase content induced by increasing Cu(2+), suggesting that superoxide dismutase failed to reduce Cu(2+) damage in Microcystis. Considering the risk of microcystin release when Microcystis membranes are destroyed as a result of Cu(2+) treatment and the stimulation effects of a low level of Cu(2+) on growth in various species, our results suggest that copper sulfate treatment for Microcystis control could be applied before midsummer when M. aeruginosa and M. viridis are not the dominant species and actual amount of Cu(2+) used to control M. wesenbergii should be much greater than 0.10 mg L(−1). |
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