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Published on: April 24, 2018
Temperature and congener structure affect the enantioselectivity of toxaphene elimination by fish
Keith A Maruya1, Kelly L Smalling, Walter Vetter
1Skidaway Institute of Oceanography, 10 Ocean Science Circle, Savannah, Georgia 31411, USA. keithm@sccwrp.org
Abstract:
Recent advances in enantioselective separation techniques have enabled scientists to investigate environmental fate processes of chiral pollutants. In this study, congener- and enantiomer-specific toxaphene residues were monitored in captive, naturally contaminated fish (Fundulus heteroclitus) to characterize the effect of temperature and compound structure on the enantioselectivity of the elimination process. A previous study performed under warm water conditions (Tmean = 25 degrees C) demonstrated relatively rapid (t(1/2) approximately = 7-14 d) and enantioselective elimination of the reductive dechlorination metabolites 2-exo,3-endo,6-exo,8,9,-10-hexachlorobornane (B6-923 or Hx-Sed) and 2-endo,3-exo,5-endo,6-exo,8,9,10-heptachlorobornane (B7-1001 or Hp-Sed). As expected, repetition of this experiment at cooler water temperatures (Tmean = 15 degrees C) resulted in a decrease in overall (i.e., both enantiomers) first-order elimination rate constants. Enantiomer fractions or ratios (EFs/ERs) during elimination, however, varied by congener, ranging from racemic for very rapidly eliminated Cl5 homologues to increasingly nonracemic for selected Cl6-Cl8 homologues (including 86-923, several unknown Cl7 compounds, B8-1414, and B8-1945). As a result, we propose a classification to describe the environmental persistence of chiral toxaphene pollutants based on congener-specific elimination kinetics and susceptibility to biotransformation as measured by EFs/ERs.
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