4.7 Article

Incorporating bioavailability into toxicity assessment of Cu-Ni, Cu-Cd, and Ni-Cd mixtures with the extended biotic ligand model and the WHAM-Ftox approach

期刊

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
卷 22, 期 23, 页码 19213-19223

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-015-5130-2

关键词

Bioavailability; Toxicity; Metals; Mixture interactions; WHAM-F-tox; Biotic ligand model

资金

  1. Belgian Federal Science Policy Office (BELSPO) [3E150127]

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There are only a limited number of studies that have developed appropriate models which incorporate bioavailability to estimate mixture toxicity. Here, we explored the applicability of the extended biotic ligand model (BLM) and the WHAM-F-tox approach for predicting and interpreting mixture toxicity, with the assumption that interactions between metal ions obey the BLM theory. Seedlings of lettuce Lactuca sativa were exposed to metal mixtures (Cu-Ni, Cu-Cd, and Ni-Cd) contained in hydroponic solutions for 4 days. Inhibition to root elongation was the endpoint used to quantify the toxic response. Assuming that metal ions compete with each other for binding at a single biotic ligand, the extended BLM succeeded in predicting toxicity of three mixtures to lettuce, with more than 82 % of toxicity variation explained. There were no significant differences in the values of f (mix50) (i.e., the overall amounts of metal ions bound to the biotic ligand inducing 50 % effect) for the three mixture combinations, showing the possibility of extrapolating these values to other binary metal combinations. The WHAM-F-tox approach showed a similar level of precision in estimating mixture toxicity while requiring fewer parameters than the BLM-f(mix) model. External validation of the WHAM-F (tox) approach using literature data showed its applicability for other species and other mixtures. The WHAM-F (tox) model is suitable for delineating mixture effects where the extended BLM also applies. Therefore, in case of lower data availability, we recommend the lower parameterized WHAM-F-tox as an effective approach to incorporate bioavailability in quantifying mixture toxicity.

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