If the standard procedures are used to measure the incipient LC50 for different species of fish will there still be a large variability in toxicity data? The LC50 steady state is proportional to the concentration of contaminant in the tissue of the organism that causes the adverse effect, so if the LC50 steady state is measured for different species, there shouldn't be much variability, is that right? If that is the case then does using a tissue residue approach still help reduce variability in toxicity data compared to measuring the contaminant in water?