Polybrominated Biphenyl Ethers Research Articles

Non-target screening analysis of hazardous noxious substances using gas chromatography-quadrupole time-of-flight mass spectrometry

The forensic investigation of hazardous noxious substances (HNS) is paramount for an effective response to chemical spill emergencies and other accidents. Analyzing unknown emergency samples poses a challenge due to the limited availability of background information, making the selection of appropriate sample preparation and analytical methodologies difficult. The utilization of high-resolution mass spectrometers (HRMS) in screening both target and non-target substances proves instrumental in revealing hazardous substances that may be overlooked alongside the intended analytes. In this study, a gas chromatography-quadruple time-of-flight mass spectrometer (GC-QTOF-MS) was employed to identify numerous organic compounds in an indoor dust sample. The compounds detected encompassed normal alkanes, fatty acids (saturated and unsaturated), alcohols, phenols, sterols, drugs, polycyclic aromatic hydrocarbons (PAHs), pesticides, flame retardants (such as polybrominated biphenyl ethers, PBDEs), plasticizers (such as phthalates and phosphates), among others. Notably, concentrations of n-alkanes, fatty acids, and phthalates were relatively high, while PAHs and pesticides were present at trace levels. The application of GC-QTOF-MS provides a swift and confirmative approach for analyzing target, suspect, and non-target compounds in both routine and emergency scenarios. This methodology proves invaluable in enhancing our capability to comprehensively assess and address chemical incidents, ensuring a more thorough and accurate response.

Preferential association of PBDEs and PAHs with mineral particles vs. dissolved organic carbon: Implications for groundwater contamination at e-waste sites

Polybrominated biphenyl ethers (PBDEs) and polycyclic aromatic hydrocarbons (PAHs) are commonly detected contaminants at e-waste recycling sites. Against the conventional wisdom that PBDEs and PAHs are highly immobile and persist primarily in shallow surface soils, increasing evidence shows that these compounds can leach into the groundwater. Herein, we compare the leachabilities of PBDEs vs. PAHs from contaminated soils collected at an e-waste recycling site in Tianjin, China. Considerable amounts of BDE-209 (0.3–2 ng/L) and phenanthrene (42–106 ng/L), the most abundant PBDE and PAH at the site, are detected in the effluents of columns packed with contaminated soils, with the specific concentrations varying with hydrodynamic and solution chemistry conditions. Interestingly, the leaching potential of BDE-209 appears to be closely related to the release of colloidal mineral particles, whereas the leachability of phenanthrene correlates well with the concentration of dissolved organic carbon in the effluent, but showing essentially no correlation with the concentration of mineral particles. The surprisingly different trends of the leachability observed between BDE-209 and phenanthrene is counterintuitive, as PBDEs and PAHs often co-exist at e-waste recycling sites (particularly at the sites wherein incineration is being practiced) and share many similarities in terms of physicochemical properties. One possible explanation is that due to its extremely low solubility, BDE-209 predominantly exists in free-phase (i.e., as solid (nano)particles), whereas the more soluble phenanthrene is mainly sorbed to soil organic matter. Findings in this study underscore the need to better understand the mobility of highly hydrophobic organic contaminants at contaminated sites for improved risk management.

Application of multicriteria decision analysis to assess the greenness of molecularly imprinted polymers synthesis components

The study applies multicriteria decision analysis (MCDA) to rank the components of molecularly imprinted polymers (MIPs) synthesis according to their greenness. The components are taken from papers that are describing synthesis of MIPs for persistent organic pollutants (POPs) sorbents. Functional monomers (n = 14), target/surrogate molecules (n = 10), porogens (n = 8), cross-linking agents (n = 8) and initiators (n = 4) are described with 10 criteria referring to their safety of application, toxicity, environmental persistence and bioaccumulability. The rankings are performed according to three scenarios, with the application of different weights. The ranking results give a specific guide on the selection of green synthesis components for polybrominated biphenyl ethers (PBDEs) as representatives of POPs, by identification of problematic and recommended chemicals. The results are useful in designing MIP synthesis protocols.

Research on the distribution of harmful substances in automotive products based on chemical quantitative

At present, China's automotive industry lacks standardized standards and testing methods for conducting harmful substance testing and evaluation of products.This article finely disassembled a passenger car model and conducted detection and analysis of harmful substances. More than 320000 materials were tested, involving 85 assembly components. This article studies six harmful substances in automotive materials, including lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls, and polybrominated biphenyl ethers. The content of harmful substances and their distribution in different materials and components are analyzed. This article provides technical reference for conducting hazardous substance assessments in the automotive industry through data analysis. The harmful substance mainly contained in the studied automotive product is lead, which is mainly distributed in materials such as copper alloys, aluminum, steel, solder, plastics, etc. The content of mercury, cadmium, hexavalent chromium, polybrominated biphenyls, and polybrominated biphenyl ethers in automobiles is generally low.

Biomonitoring of organic pollutants in pet dog plasma samples in North-Western Spain

Most of organic pollutants (OPs) have the ability to interfere with biological systems causing negative effects in living beings, including humans. In the last decades, pets have been used as bioindicators of human exposure because they share the same habitat with their homeowners. We sought to determine levels of approximately 70 OPs, including polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polybrominated biphenyl ethers (PBDEs), organophosphate pesticides (OPPs), polycyclic aromatic hydrocarbons (PAHs) and pyrethroids (PYRs) in plasma samples from 39 pet dogs from Ourense (north-western Spain). The results revealed that PAHs were the dominant OPs (mean value 175 ± 319 ng/g lipid weight (lw)), followed by PYRs (132 ± 352 ng/g lw), PCBs (122 ± 96 ng/g lw), OCPs (33 ± 17 ng/g lw), PBDEs (19 ± 18 ng/g lw) and OPPs (2.1 ± 2.7 ng/g lw) in plasma samples. We have previously detected the target OPs in hair samples of pets, collected simultaneously and similar trend of some OPs has been observed. Moreover, pyrene and chrysene showed correlations between levels detected in both matrices.

Global research into the relationship between electronic waste and health over the last 10 years: A scientometric analysis.

The aims of this research were to conduct the first holistic and deep scientometric analysis of electronic waste and health and provide with the prediction of research trends and hot topics. A comprehensive literature search was conducted via the Web of Science Core collection databases on 26 August 2022 to identify all articles related to electronic waste and health. A total of 652 records have been extracted from the Web of Science after applying inclusion and exclusion criteria and were analyzed using bibliometrix software of R-package, VOSviewer, and CiteSpace, visualized by tables and diagrams. The number of publications and total citations had shown a general growth trend from 2012 to 2021, with an average annual growth rate of 23.74%. Mainland China was the significant nation with the greatest number of publications, citations, and international links. The journal publishing the most was "Science of the Total Environment" (n = 56). Huo X and Hu XJ were the top two author contributing to this field with the highest h-index (23). Over time, the focus in this field shifted to exposure to heavy metal, polychlorinated biphenyls, polybrominated biphenyl ethers, and poly- and perfluorinated alkyl substances from electronic waste, and managements, such as hydrometallurgy. By this scientometric analysis, we found that the most active country, journal, organization and author contributing to this filed, as well as high impact documents and references and research hotspots. Also, we found that the hotspots might be exposure to toxic substances from electronic waste procession, its impact on human health and relevant managements. And evironmentally friendly materials to replace heavy metal mate rials, and environmentally friendly and effective recycling methods of electronic waste need to be further studied.

Behavioral changes and transcriptomic effects at embryonic and post-embryonic stages reveal the toxic effects of 2,2′,4,4′-tetrabromodiphenyl ether on neurodevelopment in zebrafish (Danio rerio)

Polybrominated biphenyl ethers (PBDEs) are new persistent pollutants that are widely exist in the environment and have many toxic effects. However, their toxicity mechanisms on neurodevelopment are still unclear. In this study, zebrafish embryos were exposed to 2, 2′, 4, 4′-tetrabromodiphenyl ether (BDE-47) (control, 10, 50 and 100 μg/L) at 2 h postfertilization (hpf) – 7 dpf. Locomotion analysis indicated that BDE-47 increased spontaneous coiling activity in zebrafish embryos under high-intensity light stimuli and decreased locomotor in zebrafish larvae. RNA-Seq analysis revealed that most of the up-regulated pathways were related to the metabolism of cells and tissues, while the down-regulated pathways were related to neurodevelopment. Consistent with the locomotion and KEGG results, BDE-47 affected the expression of genes for central nervous system (gfap, mbpa, bdnf &pomcb), early neurogenesis (neurog1 & elavl3), and axonal development (tuba1a, tuba1b, tuba1c, syn2a, gap43 &shha). Furthermore, BDE-47 interfered with gene expression of the Wnt signaling pathway, especially during embryonic stages, suggesting that the mechanisms of BDE-47 toxicity to zebrafish at various stages of neurodevelopment may be different. In summary, early neurodevelopment effects and metabolic disturbances may have contributed to the abnormal neurobehavioral changes induced by BDE-47 in zebrafish embryos/larvae, suggesting the neurodevelopmental toxicity of BDE-47.

Applying the Global Monitoring Plan and analysis of POPs results in atmospheric air in Mexico (2017-2018).

Air is one of the target matrices of the Global Monitoring Plan (GMP) of the Stockholm Convention to determine concentrations and transport of Persistent Organic Pollutants (POPs). Mexico participates in the GMP for POPs in ambient air through the AIR-Global Environment Facility (GEF) program. The objective of this study was to analyze the results of POPs monitoring of air samples collected in Los Mochis, Sinaloa, Mexico, between 2017 and 2018. Passive samplers were used for the determination of chlorinated basic POPs, indicator polychlorinated biphenyls (Ind. PCBs), polybrominated biphenyl ethers (PBDEs), polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and dioxin-like polychlorinated biphenyls (dl-PCBs). A principal component analysis was applied to determine relationships between pollutants and groups present in the ambient air of the rural study area. Of the total POPs analyzed, 85.56% were detected in ambient air samples from Mexico. Organochlorine compounds, as DDT derivatives, were identified mainly, as well as PBDEs, PCDDs, and PCDFs. The prevalence of compounds differed according to the seasonality of sampling, with no change in average concentration between monitoring years.

Increasing Trends of Legacy and Emerging Organic Contaminants in a Dated Sediment Core From East-Africa

Temporal trends of industrial organic contaminants can show how environmental burdens respond to changes in production, regulation, and other anthropogenic and environmental factors. Numerous studies have documented such trends from the Northern Hemisphere, while there is very limited data in the literature from sub-Saharan Africa. We hypothesized that the temporal trends of legacy and contemporary industrial contaminants in sub-Saharan Africa could greatly differ from the regions in which many of these chemicals were initially produced and more extensively used. For this purpose, a dated sediment core covering six decades from a floodplain system in urban Dar es Salaam, Tanzania, was analysed. The samples were analysed for selected legacy persistent organic pollutants (POPs) [polychlorinated biphenyls (PCBs) and polybrominated biphenyl ethers (PBDEs)] and chemicals of emerging concern (CECs) [alternative brominated flame retardants (aBFRs), chlorinated paraffins (CPs), and dechloranes]. All groups of chemicals showed a steep increase in concentrations towards the uppermost sediment layers reflecting the more recent years. Concentrations of the individual compound groups in surface sediment were found in the order CPs >> aBFRs ∼ ∑25PBDEs > dechloranes ∼ ∑32PCBs. Time trends for the individual compounds and compound groups differed, with ∑32PCBs showing presence in sediments since at least the early 1960s, while some CECs first occurred in sediments corresponding to the last decade. Investigations into potential drivers for the observed trends showed that socioeconomic factors related to growth in population, economy, and waste generation have contributed to increasing concentrations of PBDEs, aBFRs, CPs, and Dechlorane Plus. Further monitoring of temporal trends of industrial organic contaminants in urban areas in the Global South is recommended.

Human CYP enzyme-activated genotoxicity of 2,2′,4,4′-tetrabromobiphenyl ether in mammalian cells

Polybrominated biphenyl ethers (PBDEs) are a group of persistent organic pollutants with endocrine-disrupting, neurotoxic, tumorigenic and DNA-damaging activities. They are hydroxylated by human liver microsomal CYP enzymes, however, their mutagenicity remains unknown. In this study, 2,2′,4,4′-tetrabromobiphenyl ether (BDE-47, relatively abundant in human tissues) was investigated for micronuclei induction and DNA damage in mammalian cells. The results indicated that BDE-47 up to 80 μM under a 6 h/18 h (exposure/recovery, covering 2 cell cycles) regime did not induce micronuclei in V79-Mz and V79-derived cell lines expressing human CYP1A1 or 1A2, while it was moderately positive in human CYP2B6-, 2E1-and 3A4-expressing cell lines (V79-hCYP2B6, V79-hCYP2E1-hSULT1A1 and V79-hCYP3A4-hOR, respectively). Following 24 h exposure, BDE-47 induced micronuclei in V79-hCYP2E1-hSULT1A1 and V79-hCYP3A4 cells at increased potencies. In the human hepatoma (HepG2) cells BDE-47 (48 h exposure) was inactive up to 40 μM, however, pretreatment of the cells with ethanol (0.2%, v:v, inducer of CYP2E1) or rifampicin (10 μM, inducer of CYP3A4) led to significant micronuclei formation by BDE-47; pretreatment with bisphenol AF (100 nM) also potentiated BDE-47-induced micronuclei formation (which was blocked by a CYP2E1 inhibitor trans-1,2-dichloroethylene or a CYP3A inhibitor (ketoconazole). Immunofluorescent staining of centromere protein B with the micronuclei formed by BDE-47 in HepG2 cells pretreated with ethanol or rifampicin demonstrated selective formation of centromere-containing micronuclei. The increased phosphorylation of both histones H2AX and H3 in HepG2 by BDE-47 also indicated an aneugenic potential. Therefore, this study suggests that BDE-47 is an aneugen activated by several human CYP enzymes.

Removal of heavy metal ions and polybrominated biphenyl ethers by sulfurized nanoscale zerovalent iron: Compound effects and removal mechanism

Sulfurized nanoscale zerovalent iron (S-nZVI) has been widely reported to be able to quickly remove heavy metals/persistent organic pollutants, but the limited understanding of the complicated removal process of heavy metals-organic combined pollutants restricts the application of S-nZVI. Here, we demonstrate that there is significant difference in the effectiveness of S-nZVI for removing single pollutant and complex pollutants. The removal kinetic constant (kobs) of heavy metals by S-nZVI followed a sequence of Cr(VI)>Pb(II)>Ni(II)>Cd(II) with or without polybrominated diphenyl ethers (PBDEs). While the capacity of co-existing cations increasing the kobs of PBDEs followed the order: Ni(II)>Pb(II)>Cd(II), and the co-existence of Cr(VI) anion inhibited the reduction of PBDE by S-nZVI because the generated Cr-Fe precipitate hindered the electron transfer. The de-passivation process on S-nZVI surface by Cd(II) ions slightly accelerated the transformation rate of electron. Nevertheless, the co-existing Pb(II) significantly accelerated the transformation of BDE-209 via the galvanic effect from the generated Pb0/Fe0 bimetal. Interestingly, the kobs of BDE-47 in Ni(II)/S-nZVI system was 5.51 times higher than that of Pb(II)/S-nZVI system, implying that an atomic hydrogen mechanism dominated the reduction of BDE-47 by Ni(II)/S-nZVI. In conclusion, the results provided a deep comprehending of removal mechanism of heavy metal-organic complex pollutants by S-nZVI.

Polybrominated Diphenyl Ether in E-waste Dismantling Sites in Taizhou City, Zhejiang Province: Concentration, Distribution, and Migration Trend

The concentration of polybrominated biphenyl ethers (PBDEs) in surface soil and atmosphere of e-waste dismantling sites in Taizhou city, Zhejiang Province was determined. The concentration ranges of ∑12PBDEs in surface soil of e-waste dismantling site, farmland, and resident areas in Fengjiang Town (FJ) and Binhai Town (BH) were 21.8-1310 ng ·g-1 and 6.19-220 ng ·g-1, respectively. No significant difference was observed in the distribution of PBDEs between the FJ and BH soil. The concentration range of ∑12PBDEs in the atmosphere of FJ and BH were 262-3240 pg ·m-3 and 840-2990 pg ·m-3, respectively. The median levels of PBDEs in the atmosphere of FJ and BH were 1410 pg ·m-3 and 840 pg ·m-3 in winter and 1590 pg ·m-3 and 1960 pg ·m-3 in summer, respectively. However, a significant difference was observed in the distribution of 11 PBDE congeners, except BDE-209, during winter and summer seasons. The migration trend analysis showed the differences between the soil and air of FJ and BH. The main migration trend of 3-5-BDEs was the volatilization from soil to atmosphere, and the increase in temperature promoted the volatilization of these PBDEs from soil to atmosphere in FJ. This indicated that the PBDEs in soil had become a major source of pollution emission and suggested that soil remediation should be carried out at the e-waste dismantling site and parts of farmland in FJ. Contrary to FJ, atmospheric deposition was the major migration trend of PBDEs and the soil was the main sink of PBDEs in BH. This indicated that e-waste dismantling site in BH could be a new source of PBDEs emission in this area.

Non-invasive biomonitoring of organic pollutants using feather samples in feral pigeons (Columba livia domestica)

A large portion of organic pollutants (OPs) represent a potential hazard to humans and living beings due to their toxic properties. For several years, birds have been used as biomonitor species of environmental pollution. Polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polybrominated biphenyl ethers (PBDEs), organophosphate pesticides (OPPs), polycyclic aromatic hydrocarbons (PAHs) and pyrethroids (PYRs) were assessed in body feather samples of 71 feral pigeons (Columba livia domestica) collected from Asturias and Galicia (NW Spain). The percentage of detection for all chemical groups were above 90% in studied birds. The general pattern was dominated by PAHs (mean value ± standard deviation (SD) 32 ± 15 ng/g) followed by OCPs (3.8 ± 1.1 ng/g), PYRs (3.4 ± 3.8 ng/g), PCBs (1.6 ± 1.0 ng/g), OPPs (1.3 ± 0.70 ng/g) and PBDEs (0.80 ± 0.30 ng/g). Significant differences were observed between age, location and gender suggesting different sources of exposure and accumulation pathways.

A novel management strategy for removal and degradation of polybrominated diphenyl ethers (PBDEs) in waste printed circuit boards

Waste printed circuit boards (PCBs) contain a high level of brominated flame retardants (BFRs), among which polybrominated biphenyl ethers (PBDEs) are the most widely used additive BFRs. PBDEs are considered to be a type of persistent organic pollutants (POPs). The efficient removal/degradation of PBDEs in waste PCBs is an urgent problem in electronic waste treatment, but the degradation of PBDEs is a great challenge due to their extreme stability and persistence in nature. In this study, a novel management strategy was developed for removal and degradation of PBDEs in waste PCBs by using a simple subcritical methanol (SubCM) process. The results showed that reaction temperature, residence time, solid-to-liquid ratio, and additive NaOH are key factors influencing the removal of PBDEs from waste PCBs. Under optimal conditions (200 °C, 60 min, 1:20 g/mL), the removal efficiency of ∑8PBDEs from waste PCBs could reach 91.3% and 98.8% for the proposed process of SubCM and SubCM + NaOH, respectively. When the temperature is below 200 °C, highly brominated PBDEs congeners in waste PCBs were degraded into 2,'3,4′,6-Tetrabromodiphenyl ether (BDE71) and 2,4,4′-Tribromodiphenyl ether (BDE28) after SubCM treatment. 4-Bromophenyl ether (BDE4) and diphenyl ether were generated by the further debromination of BDE71 and BDE28 with the increase of treatment temperature. The debromination temperature of PBDEs congeners in SubCM could be markedly lowered by adding 4 g/L of NaOH. The complete debromination of PBDEs congeners in waste PCBs could be achieved at 300 °C and 250 °C for the developed process of SubCM and SubCM + NaOH, respectively.

Method optimisation for the simultaneous determination of legacy and emerging halogenated flame retardants in particulate matter collected in an electronic waste recycling facility

ABSTRACT The diffusion and the recycling of electric and electronic equipment waste (WEEE) are an important issue for industrialised countries. During treatment operations of this equipment, legacy and emerging halogenated flame retardant can be released in the environment, causing great concern for their toxicity. For this purpose, a method to simultaneously determine polybrominated biphenyl ethers, hexabromocyclododecane, 10 emerging brominated flame retardants and in parallel-polychlorinated biphenyls was optimised and applied to particulate matter samples collected within a WEEE facility. In this paper, starting from a previously published method, we drastically simplified the sample preparation, reducing the overall completion time, solvent consumption, costs and achieving adequate selectivity and sensitivity for all the target compounds. The multi–analyte method was evaluated in terms of reproducibility, linearity, recovery, limits of detection, limit of quantification, and matrix effect and compared to the previous method. Quantitative analyses were carried out by gas chromatography-mass spectrometry in negative chemical ionisation, using matrix-matched calibration curves. The reliability and robustness of the method were demonstrated through the analysis of certified and reference compounds in Standard Reference Material 2585. The most abundant compounds in particulate matter samples, collected in an electric and electronic equipment waste treatment plant, were BDE 47 (3.9 ng m−3), CB 138 (2.7 ng m−3), and 1,2-bis(2,4,6-tribromophenoxy) ethane (4.2 ng m−3).

Baby Steps Forward: Recommendations for Better Understanding Environmental Chemicals in Breast Milk and Infant Formula.

Baby Steps Forward: Recommendations for Better Understanding Environmental Chemicals in Breast Milk and Infant Formula.

Combined toxicity of organophosphate flame retardants and cadmium to Corbicula fluminea in aquatic sediments

Organophosphate flame retardants (OPFRs), as alternatives to polybrominated biphenyl ethers (PBDEs), are frequently detected in various environmental matrices. Owing to urbanization and industrial pollution, co-contamination of OPFRs and heavy metals is ubiquitous in the environment. The toxicity of OPFRs in aqueous phase is a significant concern, but uncertainty still exists regarding the co-toxicity to benthic organisms of OPFRs and metals in sediments. Hence, we explored the physiological response of Corbicula fluminea to OPFRs and Cd in sediments. The results indicated that the antioxidant system in the clams was stimulated in the presence of OPFRs and Cd, and the oxidative stress increased with increasing concentrations of OPFRs. In contrast, the cytochrome P450 (CYP450) content and acetylcholinesterase (AChE) activity were reduced by exposure to both OPFRs and Cd. The cytochrome P450 4 family (CYP4) mRNA expression and OPFR toxicity were lower than those in previously reported experiments conducted in the water phase. Moreover, the expression levels of metallothionein (MT) and AChE mRNA decreased when OPFRs and Cd were present together. The highest integrated biomarker response (IBR) index (IBR = 15.41) was observed in the presence of 45 mg kg−1 Cd + 200 mg kg−1 OPFRs, rather than the 45 mg kg−1 Cd + 400 mg kg−1 OPFRs treatment (IBR = 9.48). In addition, CYP450 and AChE in the digestive glands of C. fluminea exhibited significant correlations with the concentration of the OPFR/Cd mixture (p < 0.01) and could be effective biomarkers for OPFR and Cd co-contamination. The results potentially contribute to more realistic predictions and evaluations of the environmental risks posed by OPFRs in aquatic sediments contaminated with heavy metals, particularly with respect to the risk to benthic organisms.

Environmental Endocrine Disruptors and Neurological Disorders

We live in a world where daily exposure to environmental chemicals is inevitable. Many studies point to environmental chemicals a major cause of neurological diseases. Properly intervening in and managing the exposure requires up-to-date information about neurotoxic chemicals that may lead to neurological disorders. The recent literature on the neurotoxic effects of environmental chemicals was reviewed, including both animal and human studies. Parkinson’s disease, Alzheimer’s disease and autism are closely associated with environmental chemicals such as polychlorinated biphenys (PCBs), dioxins, polybrominated biphenyl ethers (PBDE), and perfluoroalkyls. There is strong evidence linking environmental chemical exposure to neurodevelopmental and neurodegenerative diseases. In particular, it is important to pay close attention to a high risk-age group where the window of exposure is critical to causing neurological disease. Key Words: Alzheimer disease, Parkinson disease, Neurotoxic chemicals, Endocrine disruptors

Halogenated organic pollutants in aquatic, amphibious, and terrestrial organisms from an e-waste site: Habitat-dependent accumulation and maternal transfer in watersnake

Dichlorodiphenyltrichloroethanes (DDTs), Polychlorinated biphenyls (PCBs), and halogenated flame retardants (HFRs) were measured in aquatic, amphibious, and terrestrial wildlife collected from an e-waste contaminated pond and its surrounding region. The species-specific bioaccumulation and maternal transfer of chemicals in the watersnake were investigated. Total concentrations of target chemicals ranged from 1.3 × 103 to 4.8 × 105 ng g−1 lipid weight. PCBs were the predominant (72–95%) contaminants, followed by polybrominated biphenyl ethers (PBDEs, 4–27%). The concentrations of PCBs and HFRs except decabromodiphenyl ethane (DBDPE) were higher in aquatic organisms and terrestrial birds than in amphibians and lizards. Relatively high DDT levels were observed in the terrestrial birds and toads, but high DBDPE was found in the aquatic species except for waterbird eggs. Species-specific congeners profiles for PCB and PBDE and isomeric composition for dechlorane plus were observed. These results indicated a habitat-dependent accumulation among different species. Maternal transfer examined by the ratio of egg to carcass for watersnakes indicated multi-linear correlations between maternal transfer potential and octanol-water partition coefficient (log KOW) of chemicals. The same maternal transfer efficiencies were found for chemicals with log KOW between 6 and 8, then the maternal transfer potential rapidly decreased with increasing of log KOW.

Erratum: "Hydroxylated Polybrominated Biphenyl Ethers Exert Estrogenic Effects via Nongenomic G Protein-Coupled Estrogen Receptor Mediated Pathways".

[This corrects the article DOI: https://doi.org/10.1289/EHP2387.].