4.7 Article

Diastereomer- and enantiomer-selective accumulation and depuration of 1,2-dibromo-4-(1,2-dibromoethyl) cyclohexanes (DBE-DBCHs) and 1,2,5,6-tetrabromocyclooctanes (TBCOs) in earthworms (Eisenia fetida)

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 826, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.154145

Keywords

1,2-Dibromo-4-(1,2-dibromoethyl) cyclohexane; 1,2,5,6-Tetrabromocyclooctane; Diastereomer; Enantiomer; Bioaccumulation; Earthworm

Funding

  1. National Key Research Development Plans of Special Project [2018YFC1801002]
  2. National Natural Science Foundation of China [41877479, 22076213]

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This study evaluated the accumulation and depuration of DBE-DBCH and TBCO diastereomers in earthworms and found that different diastereomers exhibited different accumulation and depuration kinetics.
Due to the regulation of hexabromocyclododecane (HBCD), much attention has been paid to its potential substitutes, 1,2-dibromo-4-(1,2-dibromoethyl) cyclohexane (DBE-DBCH) and 1,2,5,6-tetrabromocyclooctane (TBCO). DBE-DBCH and TBCO contain several diastereomers and enantiomers, which may exhibit different environmental behaviors and biological effects. In this study, the accumulation and depuration of individual DBE-DBCH and TBCO diastereomers by earthworms (Eisenia fetida) from diastereomer-contaminated soils were evaluated. The accumulation and depuration kinetics of DBE-DBCH and TBCO diastereomers followed one-compartment first-order kinetics. The biota soil accumulation factor (BSAF) of beta-DBE-DBCH (2.74 g(oc) g(lip)(-1)) was 1.26 times that of alpha-DBE-DBCH (2.18 g(oc) g(lip)(-1)), while the BSAF of beta-TBCO (2.15 g(oc) g(lip)(-1)) was 1.62 times that of alpha-TBCO (1.3 g(oc) g(lip)(-1)), showing the diastereomer-specific accumulation of DBE-DBCH and TBCO. DBE-DBCH and TBCO diastereomers appeared to be transformed in earthworm-soil systems; however, no evidence of bioisomerization of the four diastereomers in earthworms was found, and no potential metabolites of debromination and hydroxylation were detected. Furthermore, the selective enrichment of E1-alpha-DBE-DBCH and E1-beta-DBE-DBCH (E1 represents the first enantiomer eluted) occurred in earthworms as the enantiomer fractions (EFs) for alpha-DBE-DBCH (0.562-0.763) and beta-DBE-DBCH (0.516-0.647) were significantly greater than those in the technical products (0.501 for alpha-DBE-DBCH and 0.497 for beta-DBE-DBCH, p < 0.05), especially in the depuration stage. The results demonstrated the diastereomer-and enantiomer-selective accumulation of DBE-DBCH and the diastereomer-selective accumulation of TBCO in the earthworm.

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