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Toxicity of pentachlorophenol to native aquatic species in the Yangtze River
Xiaowei Jin1, Jinmiao Zha, Yiping Xu
1State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, P.O. Box 2871, Shuangqing Road 18, Haidian District, Beijing 100085, China.
Introduction:
While the literature is replete with studies of the toxic potency of pentachlorophenol (PCP), site-specific criteria for native aquatic species that can be used in ecological risk assessments has been lacking and application of toxicity information for non-native species is controversial.
Materials And Methods:
In the present study, acute and chronic toxicities of PCP to six aquatic species native to the Yangtze River were determined. The HC₅ and HC₅₀ (hazardous concentration for 5% and 50% of species) were derived from dose-response curves for these native aquatic species and were then compared with those derived for non-native species.
Results:
The acute toxicity values for the native species ranged from 8.8 × 10⁻² mg l⁻¹ (Plagiognathops microlepis) to 1.1 mg l⁻¹ (Soirodela polyrhiza), while chronic toxicity values based on no observed effect concentrations (NOECs) ranged from 0.01 mg l⁻¹ (Macrobrachium superbum) to 0.25 mg l⁻¹ (Soirodela polyrhiza). Native aquatic benthos was more sensitive to acute PCP exposure than non-native species. There was no significant difference in NOECs derived from native fish species and those based on non-native fish species. The median acute HC₅ and HC₅₀ derived from the toxicity data of native taxa were both less than those derived from non-native taxa. There was no significant difference between chronic HC₅s derived from the two sets of taxa. However, the median chronic HC₅₀ derived from native taxa was less than that derived from non-native taxa.
Conclusion:
The study upon which we report here provides site-specific toxicity information developed for native species which can be used for the protection of local aquatic life from a common contaminant, PCP.
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