POLYBROMINATED BIPHENYLS tained an unknown (Rf 0.27) in the alachlor experiment and an unknown (Rf 0.30) in the propachlor experiment (Tables III and IV). According to Lamoureux et al. (1971) and Sharp (1972), these herbicides in the plants were rapidly conjugated with nature products as transitory metabolites. Two of them have been identified as conjugates of glutathion and -glutamylcystein. Since model metabolites were not available at the time and these metabolites and degradation products did not accumulate in the food-chain organisms (Tables III and IV), no attempt was made to identify them.Total 14C was higher in organisms than in water. For example, snail accumulated 24 times more alachlor metabolites than did the water. We do not know whether this constitutes an environmentally acceptable level, but we do know that the accumulation is much less than that of organochlorine pesticides such as DDT which is concentrated over several thousand times more in organisms than in water (Metcalf et al., 1971).In summary, alachlor and propachlor were rapidly degraded in the water. There was no evidence to indicate that these two herbicides and their degradation products were magnified in the food chain. For example, the total radioactivity in a food chain from algae -* mosquito -*• fish decreased from 0.66 to 0.23 ppm in alachlor, and from 0.21 to 0.015 ppm in propachlor.
ACKNOWLEDGMENTThe provision of ring-14C-labeled alachlor and propa-chlor by Monsanto Co., St. Louis, Mo., is appreciated. The cooperation of W. F. Childers, Section of Aquatic Biology, Illinois Natural History Survey, who provided some of the aquatic organisms, is greatly appreciated. LITERATURE CITED Booth, G.