Modifications to the algal growth inhibition test for use as a regulatory assay

Abstract

AbstractBiological assays using aquatic invertebrates and fish do not necessarily predict protection levels for primary producers such as algae and aquatic macrophytes. State regulatory programs may not be protecting the environment from many phytotoxic compounds. Recent modifications of the U.S. Environmental Protection Agency's algal test were evaluated for their potential use as a regulatory assay. Primary goals of this investigation were to downsize the algal assay and to evaluate various methods of automation. Disposable microplates with 2‐ml sample wells were evaluated as an alternative testing chamber for the 96‐h growth inhibition test withRaphidocelis subcapitata(formerly known asSelenastrum capricornutum). We compared the standardized Erlenmeyer® flask test to the microplate test using CuCl2, NaCl, phenol, ZnCl2, and a surfactant. We noted improved control performance with the microplate test, whereas median inhibitory concentration values were similar for both methods. Other procedures we addressed included the use of EDTA, filtration of samples, and the effect of colored samples on algal growth. We also evaluated growth estimates by comparing manual cell counting to more automated growth estimates using fluorescence and ab‐sorbance endpoints. The use of fluorescence and absorbance measurements demonstrated reductions in replicate variability over manual counting and may offer time‐saving alternatives for laboratory analysts.