AbstractHazard assessments of chemicals in aquatic organisms often include chronic toxicity testing. The evaluation of exposure duration and of the life stages tested according to standard test methods has led to the development of shorter chronic toxicity tests. A similar evaluation of biological endpoints (i.e., survival, growth and reproduction) could result in tests that are more economical. We analyzed endpoints for 28 chemicals and seven fish species in 34 chronic toxicity studies. When all endpoints were compared, survival was equal to or more sensitive than all other endpoints 56 to 69 of the time. Individual endpoints were more sensitive than survival 19 to 61 of the time, except for reproduction, which was always more sensitive (although there were few observations). The no observed effect concentration (NOEC) for growth could be predicted from the NOEC for survival by using interendpoint correlations (r= 0.949 to 0.974). Ratios of NOECs for survival to those for all other endpoints examined were 5 or less in 93 to 96 of the comparisons (specific endpoint comparisons ranged from 80 to 100).The determination of the survival endpoint requires less time and money than does the determination of most other endpoints, and it appears adequate for hazard assessments in the initial stage of estimating chronic toxicity. However, a factor of at least 0.2 should be applied to the estimated no‐effect concentrations for survival to include other potential biologically significant effects at least 95 of the time. The factor of 0.2 is based on frequency analyses that resulted in the NOECs for survival being 5 times or less than the NOECs for most other endpoints about 95 of the time. Univariate analyses, however, indicated a range of 0.13 to 0.22 for the factor. A thorough evaluation of other published studies that contain endpoints other then survival should be conducted to define the appropriate factor more accuratel
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