Pollutants often exhibit different environmental behaviors at varying redox potentials, and the fate and microbial response of 6-OH-BDE-47 and 6-MeO-BDE-47 under these conditions remain unclear. Herein, C-labeled 6-OH-BDE-47 and 6-MeO-BDE-47 were used to investigate their fate in water-sediment systems at different redox potentials. For 6-OH-BDE-47, aerobic microorganisms and nitrate electron acceptors promoted nonextractable residues (NERs) formation and anaerobic microorganisms facilitated their release and was highest formed in the O-containing group. For 6-MeO-BDE-47, aerobic microorganisms, electron acceptors, and anaerobic microorganisms promoted NER formation, and was highest formed in the nitrate group. Microorganisms markedly promoted 6-OH/MeO-BDE-47 transformation. For 6-OH-BDE-47, the degradation followed the order nitrate group (29.6 %) > O-containing group (6.5 %) > sulfate group (1.45 %) > anaerobic group (0 %), while for 6-MeO-BDE-47, the order was O-containing group (8.8 %) > nitrate group = sulfate group = anaerobic group (0 %). The complexity of the 6-OH-BDE-47 and 6-MeO-BDE-47 microbial community network was consistent with the results of redox potentials, where microbial networks connectivity linking were more complex under O-containing and nitrate conditions. Overall, our study comprehensively revealed the fate of 6-OH-BDE-47 and 6-MeO-BDE-47 under different redox conditions, showing that electron acceptors can alter microbial community structure and regulating interactions. It provided guidelines for selecting electron acceptors in the remediation of 6-OH-BDE-47 and 6-MeO-BDE-47.
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http://dx.doi.org/10.1016/j.jhazmat.2024.136663 | DOI Listing |
Sci Total Environ
December 2024
University of Hohenheim, Institute of Food Chemistry, Department of Food Chemistry (170b), D-70599 Stuttgart, Germany. Electronic address:
Methoxylated polybrominated diphenyl ethers (MeO-BDEs) are a class of environmentally relevant halogenated natural products. The two most relevant isomers, 2'-MeO-BDE 68 and 6-MeO-BDE 47, were repeatedly detected at levels comparable with persistent organic pollutants in marine environmental and food samples. MeO-BDEs were suspected to be biosynthesized by bromoperoxidases through the merging of two bromophenol units, three of which (2,4-dibromophenol, 2,6-dibromophenol and 2,4,6-tribromophenol) are abundant in marine environments, followed by O-methylation to give MeO-BDEs.
View Article and Find Full Text PDFJ Hazard Mater
November 2024
School of Engineering, China Pharmaceutical University, Nanjing 210009, China. Electronic address:
Sci Total Environ
January 2023
College of Grassland, Resources and Environment, Inner Mongolia Agricultural University, Inner Mongolia Key Laboratory of Soil Quality and Nutrient Resource, Hohhot 010018, China; Key Laboratory of Agricultural Ecological Security and Green Development at Universities of Inner Mongolia Autonomous, Hohhot 010018, China.
As a class of persistent organic pollutant, polybrominated diphenyl ethers (PBDEs) and their hydroxylated and methoxylated derivatives (OH-PBDEs and MeO-PBDEs) have been widely detected in soil environments. However, studies on the bioavailability and transformation of PBDEs and their derivatives in soil organisms remain scarce. In this study, a detailed kinetic investigation on the accumulation and biotransformations of BDE-47, 6-MeO-BDE-47 and 6-OH-BDE-47 in earthworms (Eisenia fetida) exposed to artificially contaminated soils was conducted.
View Article and Find Full Text PDFChemosphere
February 2022
Key Laboratory of Drug Quality Control and Pharmacovigilance (Ministry of Education) & School of Engineering, China Pharmaceutical University, Nanjing, 210009, China. Electronic address:
As endocrine disrupting chemical, 2,2',4,4'-tetrabromodiphenyl ether (BDE-47) is widely distributed in water environment with a high detection rate. 6-hydroxy-2,2',4,4'-tetrabromodiphenyl ether (6-OH-BDE-47) and 6-methoxy-2,2',4,4'-tetrabromodiphenyl ether (6-MeO-BDE-47) are two main derivatives of BDE-47. To explore the aquatic risk of BDE-47 and its derivatives, the effects of them and their ternary mixture on the reproduction, growth, energy allocation, and neurological and antioxidant responses of Daphnia magna were monitoring during different exposure periods, i.
View Article and Find Full Text PDFChemosphere
June 2018
State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China.
Two metabolites, OH-BDEs and MeO-BDEs, of polybrominated diphenyl ethers (PBDEs) were ubiquitously detected in animal tissues and environmental samples, drawing a widely public concern to their toxicity. The comparison of toxicity between PBDEs and their metabolites has been a focus in recent years, however, comparisons seldom involve neurobehavioral toxicity of PBDEs metabolites in published works. In this study, zebrafish larvae were exposed to 6-OH-BDE-47 and 6-MeO-BDE-47 and their neurobehavioral traits (including locomotion, path angle, and social activity) were recorded using the instrument Zebrabox; meanwhile, light illumination was used as stimuli in the test duration.
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