Development of methods for evaluating toxicity to freshwater ecosystems.

This article presents a summary of a collaborative research program involving five European research groups, that was partly funded by the European Commission under its Environmental Research Program. The objective of the program was to develop aquatic toxicity tests that could be used to obtain data for inclusion at Level 2 of the Risk Evaluation Scheme for the Notification of Substances as required by the 7th Amendment to EC Directive 79/831/EEC. Currently only a very limited number of test methods have been described that can be used for this purpose and these are based on an even smaller number of test species. Tests based upon algae (Chlamydomonas reinhardi, Scenedesmus subspicatus, and Euglena gracilis), protozoa (Tetrahymena pyriformis), rotifera (Brachionus calyciflorus), crustacea (Gammarus pulex), and diptera (Chironomus riparius) were developed. The tests encompassed a range of end points and were evaluated against four reference chemicals: lindane, 3, 4-dichloroaniline (DCA), atrazine, and copper. The capacity of the tests to identify concentrations that are chronically toxic in the field was addressed by comparing the effects threshold concentrations determined in the laboratory tests with those determined for similar and/or related species and end points in stream and pond mesocosm studies. The lowest no-observed-effect concentrations (NOEC), EC(x), or LC(x) values obtained for lindane, atrazine, and copper were comparable with the lowest values obtained in the mesocosms. The lowest chronic NOEC determined for DCA using the laboratory tests was approximately 200 times higher than the lowest NOEC in the mesocosms.

A pond mesocosm study to determine direct and indirect effects of lindane on a natural zooplankton community.

We assessed the threshold concentrations for toxic effects by lindane on a zooplankton community using mesocosms in a natural pond. Enclosures (1000 litres) were treated to give mean concentrations of 0, 2, 6, 12, 18, 24, and 50 microg litre(-1) over a test period of 39 days. Larvae of the phantom midge Chaoborus flavicans showed a high susceptibility to lindane and were virtually eliminated from enclosures with > or =12 microg litre(-1) 4 days after application. Populations of cyclopoid nauplii (Eucyclops serrulatus) were reduced at a lindane concentration of 2 microg litre(-1) and showed high mortality after 11 days exposure to > or =6 g litre(-1). No lindane-induced effects could be seen in the cladoceran species Daphnia longispina and Chydorus sphaericus. Rotifer species were probably not directly affected by lindane; however loss of the principal predator Chaoborus was accompanied by an increase in the numbers of Asplanchna priodonta. A simultaneous decrease in Keratella quadrata possibly reflected predation since its decline showed no dose-response relationship with lindane and it is among the major prey of Asplanchna. Such complex secondary effects, occurring through trophic interactions between a predator and two co-occurring prey, would not have been predicted from single-species toxicity tests. These, and effects on cyclopoid populations that occurred predominantly through the mortality of nauplii, demonstrate the value of toxicological studies on natural communities. We conclude that a combination of laboratory and field investigations, coupled with mono-species and community assessments, provide the best route for understanding the effects of toxicants such as lindane for regulatory purposes.

Toxicity of lindane to freshwater insect larvae in compartments of an experimental pond.

The acute and chronic toxicities of lindane to larvae of the freshwater insects Chironomus riparius Meigen, Chaoborus flavicans (Meigen), and Sigara striata (L.) were investigated in mesocosm compartments of an experimental pond. The following median lethal concentrations (LC50s) were determined: 240-hr LC50 of 2.0 micrograms lindane liter-1 for second instar C. riparius, 72-hr LC50 of 6.5 micrograms lindane liter-1 for fourth instar C. riparius, and 96-hr LC50s of 4.0 and 3.9 micrograms lindane liter-1 for fourth instar C. flavicans and fourth or fifth instar S. striata, respectively. Lindane significantly reduced the growth over 10 days of second instar C. riparius compared to that of the control at the treatment concentrations where larvae survived (1.0, 2.5, and 7.0 micrograms lindane liter-1). A significant increase in the median emergence time in comparison to that of the control was observed for C. riparius exposed to 0.8 and 2.0 micrograms lindane liter-1, with higher concentrations causing 100% mortality. The findings compare well with previously reported laboratory data on the toxicity of lindane to insects and support the methodology and results of a laboratory growth test for C. riparius.