Allen W. Olmstead

Toxicity assessment of environmentally relevant pollutant mixtures using a heuristic model

Abstract In this study, 9 chemicals were chosen from a recent report on surface water concentrations of a variety of xenobiotics to test the hypothesis that the toxicity of chemical mixtures could be estimated using a model based on the toxicity of the individual chemicals. Concentration-response curves for the endpoints of lifespan, growth rate, and fecundity were generated for each chemical experimentally using the crustacean, Daphnia magna. From this data, a mathematical model for the combined toxicity of these chemicals was generated that merged the concepts of concentration addition and independent joint action. Toxicity of a mixture was modeled at various levels at which the ratio of the chemicals within the mixture was maintained at that reported for median detected environmental levels. Toxicity of the mixture was then determined experimentally and compared to model predictions. The model accurately predicted the most sensitive endpoint, as well as the lowest toxic effect level of the mixture. Results demonstrated that, for this mixture of chemicals, toxicity was not influenced significantly by interactions among the chemicals and a single constituent dominated toxicity. According to model predictions and experimental results, the median detected environmental concentrations of chemicals constituting this mixture provided no margin of safety.

Stress signaling: coregulation of hemoglobin and male sex determination through a terpenoid signaling pathway in a crustacean.

SUMMARY Environmental signals can activate neuro-endocrine cascades that regulate various physiological processes. In the present study, we demonstrate that two responses to environmental stress signaling in the crustacean Daphnia magna - hemoglobin accumulation and male offspring production - are co-elevated by the crustacean terpenoid hormone methyl farnesoate and several synthetic analogs. Potency of the hormones with respect to the induction of both hemoglobin and male offspring was highly correlated, suggesting that both processes are regulated by the same terpenoid signaling pathway. Six clones of the D. pulex/pulicaria species complex that were previously characterized as unable to produce male offspring and five clones that were capable of producing males were evaluated for both hemoglobin induction and male offspring production in response to methyl farnesoate. Four of the five male-producing clones produced both hemoglobin and male offspring in response to the hormone. Five of the six non-male-producing clones produced neither hemoglobin nor males in response to the hormone. These results provide additional evidence that both physiological processes are regulated by the same signaling pathway. Furthermore, the results indicate that the non-male-producing clones are largely defective in some methyl farnesoate signaling component, downstream from methyl farnesoate synthesis but upstream from the genes regulated by the hormone. A likely candidate for the site of the defect is the methyl farnesoate receptor. As a consequence of this defect, non-male-producing clones have lost their responsiveness to environmental signals that are transduced by this endocrine pathway. This defect in signaling would be likely to enhance population growth in stable environments due to the elimination of males from the population, assuming that other processes critical to population growth are not also compromised by this defect.