-
[show abstract]
[hide abstract]
ABSTRACT: A purification method for lower polybrominated diphenyl ethers (PBDEs, from tri- to hexa-BDE) in sediment for compound-specific isotope analysis (CSIA) was developed in this study. The compounds were extracted using a Soxhlet apparatus with addition of activated alumina and Florisil in the paper tube during the Soxhlet extraction provided for less complex extracts. Then, the extract was isolated from polar compounds using a multi-layer silica gel column, separated into different fractions using alumina/silica (Al/Si) gel columns and finally purified using a Florisil column. The mean recoveries of the major PBDE congeners in the spiked samples ranged from 76.2% to 82.4%. The purity of the samples was verified by GC-MS in full scan mode. The stable isotopic integrity of the spiked samples after the purification was tested by comparing the stable carbon isotope ratios (δ(13)C) of the processed and the unprocessed standard materials. The differences in the δ(13)C values for each compound between the processed and unprocessed standards were less than 0.5‰, with the exception of BDE100 (0.54‰). Finally, the purification and isotope analysis method was successfully applied to measure the δ(13)C of PBDEs in sediments. This application of the method indicated that CSIA seems to be a promising method for providing intrinsic characteristics for further environmental fate studies of PBDEs.
Talanta 07/2013; 111C:93-7. · 3.79 Impact Factor
-
[show abstract]
[hide abstract]
ABSTRACT: Two fish species (mud carp and northern snakehead) forming a predator/prey relationship and sediment samples were collected from a pond contaminated by e-waste. The concentrations and stable carbon isotope ratios (δ13C) of individual polychlorinated biphenyl (PCB) and polybrominated diphenyl ether (PBDE) congeners were measured to determine if compound-specific carbon isotopic analysis (CSIA) could be used to provide insight into the metabolism and trophic dynamics of PCBs and PBDEs. Significant correlations were found in the isotopic data of PCB congeners between the sediment and the fish species and between the two fish indicating identical origin of PCBs in sediment and fish. Most PCB congeners in the fish species were enriched in 13C compared with the PCB congeners in the sediments as a result of isotopic fractionation during the metabolism of PCBs in fish. The isotopic data of several PCB congeners showing isotopic agreement or isotopic depletion could be used for source apportionment or to trace the reductive dechlorination process of PCBs in the environment. The PCB isotopic data co-varied in the northern snakehead with in the mud carp when compared to the sediment, implying that a similar isotopic fractionation occurs from the prey to the predator fish for a PCB congener possibly due to similar metabolic pathways. The PBDE congener patterns differed in the three sample types with a high abundance of BDE209, 183, 99, and 47 in the sediment, BDE47, 153, and 49 in the mud carp and BDE47, 100, and 154 in the northern snakehead. The isotopic change of BDE congeners, such as BDE47 and BDE49, in two fish species, provides evidence for biotranformation of PBDEs in biota. The results of this study suggest that CSIA is a promising tool for deciphering the fate of PCBs and PBDEs in the environment.
Environmental Science & Technology 04/2013; · 4.80 Impact Factor
-
[show abstract]
[hide abstract]
ABSTRACT: The debromination and trophic dynamics of PBDEs in fish and whether or not compound-specific isotopic analysis (CSIA) can be used to trace these processes were investigated. Two predator/prey relationships were established in laboratory by two predatory fish species, oscar fish (OF) and redtail catfish (RF) feeding on tiger barb (TB) exposed to a commercial PBDE mixture. Metabolic debromination of PBDEs was observed in the TB and the OF, but not in the RF. The calculated biomagnification factors (BMFs) were uniform for most of the congeners in RF/TB but varied in OF/TB, which can be attributed to the metabolic debromination in the OF. The δ(13)C values of BDE47 and BDE28 were lower in fish than in those in the commercial mixture but the δ(13)C values of BDE99 were slightly higher. These results indicated that CSIA can be used to trace the biotransformation of PBDEs in biota.
Environmental pollution (Barking, Essex: 1987) 02/2013; 176C:36-41. · 3.43 Impact Factor
-
[show abstract]
[hide abstract]
ABSTRACT: A separation and isotopic analysis method was developed to accurately measure the stable carbon isotope ratios of polybrominated diphenyl ethers (PBDEs) with three to six substituted bromine atoms in fish samples. Sample extracts were treated with concentrated sulfuric acid to remove lipids, purified using complex silica gel column chromatography, and finally processed using alumina/silica (Al/Si) gel column chromatography. The purities of extracts were verified by gas chromatography and mass spectrometry (GC-MS) in the full-scan mode. The average recoveries of all compounds across the purification method were between 60% and 110%, with the exception of BDE-154. The stable carbon isotopic compositions of PBDEs can be measured with a standard deviation of less than 0.5‰. No significant isotopic fraction was found during the purification of the main PBDE congeners. A significant change in the stable carbon isotope ratio of BDE-47 was observed in fish carcasses compared to the original isotopic signatures, implying that PBDE stable carbon isotopic compositions can be used to trace the biotransformation of PBDEs in biota.
Science of The Total Environment 04/2012; 425:208-13. · 3.29 Impact Factor
-
[show abstract]
[hide abstract]
ABSTRACT: The gastrointestinal absorption, metabolic debromination, and hydroxylation of three commercial brominated diphenyl ether (BDE) mixtures were separately studied in juvenile common carp. The absorption rate of penta-BDE was higher than that of octa- and deca-BDE, likely because of the lower molecular volumes of its major congeners. However, no significantly positive relationships were found between the number of bromine atoms and the absorption rate, especially for congeners with a bromine atom number larger than six. The major congeners in fish carcass were, respectively, BDE-47 and BDE-100 in the penta-BDE exposure; BDE-154, -155, -149, and BDE-153 in the octa-BDE exposure; and BDE-154, -155, -149, -188, -179, and BDE-202 in the deca-BDE exposure. Congeners with at least one meta- or para- doubly flanked bromine atom easily undergo metabolic debromination in fish. None of the targeted MeO-polybrominated diphenyl ether (PBDE) congeners were detected in serum samples, implying that the methylation of OH-PBDE is not likely occurring in fish. Eleven OH-PBDEs and several unidentified OH-PBDE congeners were found in penta-BDE-exposed fish. The similar level among three mono-OH-BDE47 congeners suggested that the position of OH in the phenyl ring is not selective. The hydroxylation is not a significant metabolic pathway compared with debromination. No OH-PBDE congeners were found in the serum samples from deca-BDE-exposed fish, which may attributable to the low level of PBDE precursors in fish.
Environmental Toxicology and Chemistry 12/2011; 31(4):731-8. · 2.81 Impact Factor
