The role of biotic and abiotic degradation processes during the formation of typical toxaphene peak patterns in aquatic biota.

Toxaphene residues in cod liver and fish oil samples from different countries have been analyzed by HRGC-ECD and HRGC-MS as well as with multidimensional gas chromatography. The results have been compared to patterns obtained by photolysis and microbial degradation of selected single chlorobornanes and technical toxaphene. Enantiomeric ratios of the components Parlar #44 and #62 showed significant deviations from 1, indicating metabolism in cod fish and perhaps other species at least for some congeners. Parlar #50 was found to be a racemate, which corresponds to its known stability under biotic and abiotic conditions.

Multidimensional gas chromatographic enantiomer quantification of some chlorinated xenobiotics in cod liver and fish oils.

Four chiral HRGC column systems for the separation of selected organochlor pesticides and photoconversion products (heptachlor, cis- and trans-chlordane, o,p'-DDT, o,p'-DDD, and alpha-HCH) were tested. Cod hver oil and fish oil samples from different countries were comparatively analyzed. Of all these columns, the fourth was the most suitable one for the analysis of the selected compounds. The enantiomer ratios [ER] of cis-chlordane, trans-chlordane, photodieldrin, alpha-HCH, and o,p'-DDD in fish oils are nearly 1.0, while the ERs of the same substances are significantly different from 1.0 in cod liver oils. Contrary to that, the ER values of o,p'-DDT are remarkable different from 1 in the cod liver oils as well as in the fish oils.