Dechlorane Plus Research Articles

The sources of Dechlorane Plus (DP) in surface sediment from Bohai Sea and the northern part of the Yellow Sea, China: Evidence from the fractional abundance of anti-DP ([formula omitted]) combined with lignin biomarker

Dechlorane Plus (DP) is a highly chlorinated flame retardant that exists widely in the environment. In the present study, we studied the distribution, potential sources and inventory of DP in surface sediment samples from Bohai Sea (BS) and the northern part of the Yellow Sea (NPYS), China. The concentrations of DP in surface sediments ranged from 19.90 to 118.5 pg/g dry weight (dw), with a mean value of 57.30 pg/g dw (excluding K3 station), which are in general lower than most of the previously reported values in other regions. The highest DP concentration appeared at K3 station near the city of Dalian, and the next high concentration occurred in the mud area of the eastern Bohai Bay. We used an integrated approach, in which the traditional fractional abundance of anti-DP (fanti) was combined with terrestrial biomarker lignin, to identify sources of DP in the region. We found that DP in the estuarine area was mainly from the Yellow River input. Similarly, Yalu River input was the major contributor of DP in NPYS. On the other hand, DP in the mud area of the eastern Bohai Bay was mainly from atmospheric deposition and the hydrodynamic transport. The sedimentary burden of DP for the surface sediment of a thickness of 3 cm in BS and NPYS was estimated to be 254.4 kg, with a spatial density of 17.20 pg/cm2.

Effects of dechlorane plus on intestinal barrier function and intestinal microbiota of Cyprinus carpio L

Dechlorane Plus (DP) is a typical polychlorinated flame retardant that has been emerged in chemical products. Due to its accumulation and amplification effect, the toxicity of DP has become a widespread environmental safety issue. However, whether DP can affect the intestinal tract of teleost fish remains largely unclear. To understand its effects on the intestinal barrier, morphological characteristics and intestinal microbiome of common carp, different concentrations (30, 60 and 120 μg/L) of DP were exposed to common carps for 4 weeks. The results indicated that DP evidently shortened the intestinal folds and damaged the intestinal epithelium layer. In addition, the mRNA expression levels of occludin, claudin-2 and zonula occludens-1 (ZO-1) were significantly decreased with increasing DP concentrations. Furthermore, the relative abundance of some microbiota species were also changed significantly. Our study first demonstrated that DP could cause damage to the intestinal epithelium and destroy the intestinal barrier and increase the relative abundance of pathogenic bacteria, thereby increasing the probability of contact between intestinal epithelium and pathogenic bacteria, which in turn lead to an increased susceptibility to various diseases and poor health. In summary, our findings reveal that chronic DP exposure can have a harmful effect on the intestinal flora balance and is potentially linked to human disease.

Time trend of exposure to dechloranes: Plasma samples of German young adults from the environmental specimen bank collected from 1995 to 2017.

Dechloranes, like Dechlorane Plus® are commonly used flame retardants identified by the EU as substances of very high concern (SVHC) because of their persistence and bioaccumulation potential. To characterize the dechlorane exposure of Germans in the last two decades, 180 archived blood plasma samples of the German Environmental Specimen Bank (students aged 20-29 years) collected at six time points between 1995 and 2017 were analyzed for four dechloranes; namely Dechlorane Plus® (syn- and anti-DDC-CO), dechlorane 602 (DDC-DBF), and dechlorane 603 (DDC-Ant). These were quantified using a GC-MS/MS method. Overall, anti- and syn-DDC-CO were detected in 88% and 98% of the samples, whereas DDC-DBF and DDC-Ant were found in 40% and 37% of the samples, respectively. The median (95th percentile) values were 1.0ng/g lipid weight (l.w.) (3.0ng/g l.w.). for anti-DDC-CO, 0.6ng/g l.w (1.9ng/g l.w.). for syn-DDC-CO, 0.1ng/g l.w (0.6ng/g l.w.). for DDC-DBF, and 0.1ng/g l.w (0.2ng/g l.w.). for DDC-Ant. The 95th percentile concentrations of the sum of syn- and anti-DDC-CO decreased from 4.2ng/g l.w. in 1995, to 2.9ng/g l.w. in 1999, and subsequently increased to 3.7ng/g l.w. in 2008, and up to 5.9ng/g l.w. in 2017. A statistically significant decrease with time was observed for DDC-DBF and DDC-Ant, but not for DDC-CO. Our medians found in blood samples in 2017 are similar to those observed in Germany in 2013/14, but higher compared to values reported in other European countries. Overall, more toxicological and monitoring data is needed to better characterize the potential impact on health.

Investigating the presence of emerging and legacy POPs in European domestic air

Presence of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs) and dechlorane plus (DP) were evaluated in indoor domestic air from four European countries (Belgium, Italy, Spain and Portugal). The main pollutants were hexachlorohexanes (sum of α-, β- and γ-HCH; ΣHCHs) and ΣPCBs (sum of PCB-28, 52, 101, 118, 138, 153 and 180), with median concentrations of 366 and 306 pg/m3, respectively. By decreasing order came hexachlorobenzene (HCB; 130 pg/m3), ΣDDXs (sum of DDTs, DDEs and DDDs; 94.4 pg/m3), ΣPBDEs (sum of BDE-17, 28, 47, 66, 99, 100, 153, 154, 183, 206, 207 and 209; 6.08 pg/m3) and DP (0.30 pg/m3). Lower ΣPCBs and ΣDDXs levels were found at Portuguese homes compared to Belgian, Italian and Spanish households. Italian samples presented also lower ΣHCHs concentrations while Spanish homes revealed higher HCB and BDE-209 indoor air concentrations than those obtained in the other countries. ΣHCHs, ΣDDXs and ΣPBDE levels mirrored lindane, dicofol and Penta-, DecaBDE use, respectively. The influence of building characteristics, surroundings and inhabitants habits on pollutant air concentrations was investigated. Data generated were used to conduct a human exposure assessment for toddlers and adults with median (P50) and upper (P95) concentrations. Results indicated that health risk posed by inhalation of ΣPCBs, ΣHCHs, ΣDDXs, HCB, ΣPBDEs and DP were 2 to 5 orders of magnitude lower than oral Reference Dose (RfD) values, and 90 (PCB-28) and 12 (γ-HCH) times lower than Minimal Risk Levels (MRLs) for toddlers at the worst case scenario.

Global emissions of Dechlorane Plus

Dechlorane Plus (DP) is a chlorinated flame retardant applied in parallel to or as a replacement product for regulated flame retardants. Detection of DP in environmental media all over the world in recent years necessitates the development of detailed global emission estimates for environmental model studies. Based on production, usage and disposal data two global atmospheric emission scenarios were made with a detailed geographical distribution. The total DP emission is estimated to be 0.02 t/year and 3.2 t/year in a low and high emission scenario, respectively, reflecting the uncertainties in production volumes and emission factors. The emission estimates are tested by implementation in the Danish Eulerian Hemispheric Model, an advanced chemistry-transport model. An evaluation against measurements in the Arctic from the early 2010s, considered to represent background concentrations, shows that the predicted concentration range for the high emission scenario is in line with the measured range, whereas the predicted concentrations for the low emission estimate are more than a factor of 100 lower than the measurements, rendering the high emission estimate most probable.

Transfer of dechlorane plus between human breast milk and adipose tissue and comparison with legacy lipophilic compounds

In this study, levels of dechlorane plus (DP) in breast milk and matched adipose tissue samples were measured from 54 women living in Wenling, China. Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were measured simultaneously for comparison. The levels of ∑DPs/∑PBDEs varied from less than one to several dozens of ng g−1 lipid weight (lw) in matrices and the levels of ∑PCBs varied between several to hundreds of ng g−1 lw. In the same matrix, ∑DPs and ∑PCBs/∑PBDEs showed a significant relationship (p < 0.05), indicating that they shared common sources. Accordingly, there was a strong association of lipid-adjusted concentrations of individual compounds (BDE-209 excluded) between matrices (p < 0.001), suggesting that breast milk could be a proxy for adipose tissue in human bioburden monitoring of these compounds. The predicted lipid-adjusted milk/adipose ratios varied from 0.62 to 1.5 but showed significant differences (p<0.001) between compounds, suggesting a compound-specific transfer between milk lipids and adipose tissue lipids. Specifically, the milk/adipose ratios for syn-DP and anti-DP (−1.40 and 1.3, respectively) were significantly higher than those of CB congeners and hexa/hepta-BDE congeners (p < 0.05). In addition, unlike PCBs/PBDEs (excluding BDE-209), DP’s hydrophobicity might not be responsible for its preferable distribution in milk lipids. Instead, the interaction with nonlipid factors played a key role. The fraction of anti-DP between the two kinds of matrices was not significantly different, suggesting that the biochemical transfer processes may not be efficient enough to distinguish DP isomers. Nevertheless, the congener patterns of PCBs/PBDEs gave a clue about the compound-specific transfer between milk and adipose tissue. To our knowledge, this is the first to report the relationships of DP between adipose tissue and breast milk. These results could provide useful and in-depth information on biomonitoring of DP and facilitate the understanding of the accumulation and excretion potentials of DP and its distribution-related mechanism in humans.

Full-scale evaluation of reversed A2/O process for removal of multiple pollutants in sewage

This study evaluated the removal of multiple pollutants, i.e., polybrominated diphenyl ethers (PBDEs), novel halogenated flame retardants (HFRs), sulfonamide antibiotics (SAs), and heavy metals (HMs), by a full-scale reversed A2/O process in a sewage treatment plant (STP) in Guangzhou, China. The reversed A2/O process demonstrated high removal efficiencies (REs) for total PBDEs (60.5% ± 4.3%), novel HFRs (98.4% ± 2.8%) and HMs (70.1% ± 1.2%), and a relatively low RE for SAs (25.0% ± 2.3%). BDE 209, the dominant PBDE congener, showed a high residual concentration (13.41 ± 5.18 ng/L) in the suspended particulate matter (SPM) of treated effluents. Some novel HFRs, dechlorane plus (DP) and decabromodiphenyl ethane (DBDPE), were detected in the SPM of the raw sewage (7.50 ± 4.14 ng/L and 11.52 ± 11.65 ng/L, respectively). The removal of SAs was mainly through biodegradation in the activated sludge bioreactors (ASBs). Of the HMs, Mn and Ni exhibited the lowest REs (47.5% ± 2.2% and 35.0% ± 2.6%, respectively), while Cr and Cu showed the highest removal (REs > 80%). In terms of treatment units in the reversed A2/O process, ASBs showed the highest RE (27.8%) for the multiple pollutants. The information can aid in our understanding of removal properties of STPs on various pollutants and evaluating the ecological/health risks of STPs as point pollutant sources

Exposure to Low Doses of Dechlorane Plus Promotes Adipose Tissue Dysfunction and Glucose Intolerance in Male Mice.

The prevalence of type 2 diabetes (T2D) continues to increase worldwide. It is well established that genetic susceptibility, obesity, overnutrition and a sedentary life style are risk factors for the development of T2D. However, more recently, studies have also proposed links between exposure to endocrine-disrupting chemicals (EDCs) and altered glucose metabolism. Human exposure to environmental pollutants that are suspected to have endocrine disruptor activity is ubiquitous. One such chemical is Dechlorane Plus (DP), a flame retardant, that is now detected in humans and the environment. Here we show that exposure of mice to low, environmentally relevant doses of DP promoted glucose intolerance in mice fed a high-fat diet independent of weight gain. Furthermore, DP had pronounced effects on the adipose tissue, where it induced the development of hypertrophied white adipose tissue (WAT), and increased serum levels of resistin, leptin, and plasminogen activator inhibitor-1. In addition, DP exposure induced "whitening" of brown adipose tissue (BAT), and reduced BAT uncoupling protein 1 expression. Importantly, some of these effects occurred even when the mice were fed a regular, low-fat, diet. Finally, WAT adipogenic markers were reduced with DP treatment in the WAT. We also show that DP directly inhibited insulin signaling in murine adipocytes and human primary subcutaneous adipocytes in vitro. Taken together, our results show that the exposure to low and environmentally relevant levels of DP may contribute to the development of T2D.

Intergenerational transfer of Dechlorane Plus and the associated long-term effects on the structure and function of gut microbiota in offspring

The gut microbiota has been shown to be highly involved in many vital physiological processes that play key roles in human health. The intergenerational transfer of Dechlorane Plus (DP) and the complex interaction between DP and microbiota has been poorly studied. Additionally, the structural and functional effects of DP on the gut microbiota have not been studied. This study aimed to investigate the DP transfer in Sprague-Dawley rats during pregnancy and the effects of DP exposure on gut microbiota, as detected by 16S rRNA gene sequencing. The results showed that excretion in feces is a very important elimination pathway of orally dosed DP. The main intergenerational transfer pathway of DP might be via lactation rather than transplacental transport. The 16S rRNA sequencing revealed that DP exposure could decrease the richness and diversity of gut microbiota, especially at the genus level. Furthermore, in DP exposure groups, the gut microbiota production of metabolites of short-chain fatty acids was dramatically increased. The results demonstrated that DP exposure not only altered the gut microbiota structures, but also immensely influenced metabolic functions, causing long-term impact to offspring. This data indicates that more attention should be paid to the long-term health effects related to DP exposure.

Halogenated and organophosphorous flame retardants in surface soils from an e-waste dismantling park and its surrounding area: Distributions, sources, and human health risks

Electronic waste (e-waste) dismantling is an important source of flame retardant emissions, and may have potentially adverse effects on surrounding area. This study investigated their influence on the surrounding area and the human health risks after an industrial park was built in 2015 and environmentally friendly technologies were introduced at an e-waste dismantling site in South China. The concentrations of flame retardants, including polybrominated diphenyl ethers (PBDEs), polybromobenzenes (PBBzs), Dechlorane plus (DP), and organophosphate esters (OPEs), in the soils were measured. The results showed that soil contamination was greater in the industrial park than in the surrounding area. The PBDE concentrations were the highest with BDE209, a daca-BDE, being the dominant congener, followed by OPEs, where triphenyl phosphate levels were the highest. Furthermore, triphenyl phosphate can be used as an indicator of flame retardant emissions during e-waste dismantling in this region. The fanti value of DP was stable at around 0.75. The principal component analysis showed that direct emission was the major source of pollutants in the industrial park. The direct emission proportion decreased in the surrounding area, but migration and transformation increased. None of the chemicals posed a non-carcinogenic risks to children and adults via oral uptake or dermal contact when the absorption factors of the chemicals were included in the estimation. However, the total hazard quotients for children were close to a unit in the industrial park, of which, the PBDE and OPE proportions accounted for 84.2% and 15.8% of the total, respectively. However, the PBBz and DP percentages were negligible. Therefore, PBDEs and OPEs should be given more attention in the future.

Fractions Transformation and Dissipation Mechanism of Dechlorane Plus in the Rhizosphere of the Soil-Plant System.

The fractions transformation and dissipation mechanism of Dechlorane Plus (DP) in the rhizosphere of soil-plant system were investigated and characterized by a 150-day experiment using a rhizobox system. The depuration, accumulation, and translocation of DP in rice plants were observed. The contributions of plant uptake, microbial degradation, and bound-residue formation to DP dissipation under the rhizosphere effect were modeled and quantified. The gradients of DP concentrations correlated well with microbial biomass in the rhizosphere (R2 = 0.898). The rhizosphere facilitated the bioavailability of DP (excitation) and modified the bound-residue formation of DP (aging). DP concentrations in roots were positively correlated with the labile fraction of DP in soil (R2 = 0.852-0.961). There were spatiotemporal variations in the DP fractions. Dissolved and soil organic carbon were important influences on fraction transformation. Contributions to total DP dissipation were in the following ranges: microbial degradation (8.33-54.14%), bound-residue formation (3.64-16.43%), and plant uptake (0.54-3.85%). With all of these processes operating, the half-life of DP in the rhizosphere was 105 days. The stereoselectivity of DP isomers in both rice and DP fractions in soil were observed, suggesting a link between stereoselective bioaccumulation of DP in terrestrial organisms and dissipation pathways in soil.

Evidence for complex sources of persistent halogenated compounds in birds from the south China sea

Persistent halogenated compounds (PHCs), including dichlorodiphenyltrichloroethane and its metabolites (DDTs), polybrominated diphenyl ethers (PBDEs), alternative brominated flame retardants (ABFRs), and dechlorane plus (DP), were analyzed in muscle of six bird species from the South China Sea. DDTs, with concentrations up to 19,000 ng/g lipid weight (lw), were the dominant contaminants contributing to 66–99% of PHCs in birds. Concentrations of PBDEs, ABFRs, and DP ranged from 1.1 to 130, 0.73–40, and 0.21–2.5 ng/g lw, respectively. Historically pollution of DDTs and flame retardants in surrounding Asian lands were the main sources for PHCs in birds. BDE 209 was the primary PBDE congener in all birds. 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE) and decabromodiphenyl ethane (DBDPE) were the main ABFRs. Anti-DP and p,p′-DDE were the dominating compounds of DP and DDTs, respectively. Only concentrations of BDEs 153, 203, 196, and 207, p,p′-DDE, and p,p′-DDD showed significant and positive correlations with δ15N values in samples. The resident birds, red-footed booby (Sula sula), had much lower levels of p,p′-DDE and most of PBDEs than those in migratory birds from the South China Sea. Results of stable isotope ratios of carbon suggest the highly variable food items for the five migratory bird species. The abundance of DBDPE in red-footed booby might be related with the ingestion of plastic debris, which still warrants further verification.

Distribution, composition profiles, source identification and potential risk assessment of Polychlorinated Biphenyls (PCBs) and Dechlorane Plus (DP) in sediments from Liaohe Estuary

Polychlorinated biphenyls (PCBs) and Dechlorane Plus (DP) were analyzed to evaluate the environmental quality in sediments from Liaohe Estuary (LHE), northern China. The concentration of ∑24PCBs ranged from 106.7 to 270.0 pg g−1 dry weight, with a mean value of 186.6 pg g−1 in surface sediments. The PCBs concentrations in the eastern region of Gaizhou Beach (GZB) were higher than those in the western region, indicating that the effects of hydrodynamic transportation and deposition of fine-grained sediments are the factors controlling the distribution and behaviors of PCBs in LHE. Principal component analysis (PCA)-multiple linear regression (MLR) revealed that 15.9% of PCBs in LHE originated from local sources directly discharged by anthropogenic activities, 73.9% from surface runoff of eroded soils contaminated by PCBs and 10.2% from atmospheric deposition and microbial degradation. The concentration of DP varied from 10.1 to 45.7 pg g−1 dry weight, with an average value of 28.0 pg g−1 dry weight. The spatial distribution pattern of DP indicated that hydrodynamic forces and the sedimentary environment were prominent factors influencing the accumulation and distribution of DP in LHE. The mass inventories for a sediment thickness of 2 cm in the whole area of LHE were 4.1 kg and 0.6 kg for ∑24PCBs and DP, respectively. At present, the ecological risk for sediments of LHE is low for both PCBs and DP.

Uptake of halogenated organic compounds (HOCs) into peanut and corn during the whole life cycle grown in an agricultural field

Here, we elucidated the uptake and translocation of numerous halogenated organic compounds (HOCs) into corn and peanut throughout their life cycle cultivated in an agricultural field of an electronic waste recycling area, where plants were simultaneously exposed to contaminants in soil and ambient air. The geometric mean concentrations of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were 22.3 and 11.9 ng/g in peanut and 16.6 and 13.6 ng/g in corn, respectively. Decabromodiphenyl ethane (DBDPE, 6.07 ng/g) and dechlorane plus (DPs, 6.22 ng/g) also showed significant concentrations in peanuts. The plant uptake was initiated from root absorption at the emergence stage but it was subsequently surpassed by leaves absorption from the air since the late seedling stage or early reproductive stage. There was a rapid uptake of lower halogenated HOCs at the early vegetative stages in both species. However, robust uptake of highly halogenated compounds at the reproductive stages suggests a delayed accumulation of them by the plants. PBDE and PCB congener profiles suggest more noticeable tendency for inter-compartment translocation in peanut than in corn during the plant development. The DP and HBCD isomeric compositions in peanut (enriched with syn-DP and γ-HBCD) were different from those in the rhizosphere soils and air, suggesting a more stereoisomer-selective uptake and/or biotransformation in this species compared to corn. The bioaccumulation factors for root-soil and stem-root of these HOCs in most cases were <1. The tissue-distributions demonstrated that leaves serve as a significant reservoir of absorbed HOCs under the field conditions, whereas the low concentrations in peanut and corn kernels indicated translocation of most HOCs into this compartment was significantly hindered (especially for highly halogenated compounds).

Toxic effects of dechlorane plus on the common carp (Cyprinus carpio) embryonic development

Dechlorane Plus (DP) is a widely used chlorinated flame retardant, which has been extensively detected in the environment. Although DP content in the surface water is low, it can pose a continuous exposure risk to aquatic organisms due to its strong bioaccumulation. Considering that the related studies on the toxicity mechanism of DP exposure are limited, the effect of DP on carp embryo development was evaluated. In the present work, carp embryos were exposed to different concentrations (0, 30, 60, and 120 μg/L) of DP at 3 h post-fertilization (hpf). The expression levels of neural and skeletal development-associated genes, such as sox2, sox19a, Mef2c and BMP4, were detected with quantitative PCR, and the changes in different developmental toxicity endpoints were observed. Our results demonstrated that the expression levels of sox2, sox19a, Mef2c and BMP4 were significantly altered and several developmental abnormalities were found in DP-exposed carp embryos, such as DNA damage, increased mortality rate, delayed hatching time, reduced hatching rate, decreased body length, and increased morphological deformities. In addition, the activities of reactive oxygen species and malondialdehyde were remarkably higher in 60 and 120 μg/L DP exposure groups than in control group. These results suggest that DP can exhibit a unique modes of action, which lead to aberration occurrence in the early development stage of common carps, which may be related to some gene damage and oxidative stress. Besides, the parameters evaluated here can be used as tools to access the environmental risk for biota and humans exposed to DP.

Distribution behaviour in body compartments and in ovo transfer of flame retardants in North American Great Lakes herring gulls

Polybrominated diphenyl ethers (PBDEs) and other halogenated flame retardants (HFRs) continue to be an environmental concern. In the Laurentian Great Lakes, herring gulls (Larus argentatus) are an important wildlife sentinel species, although very little information is available regarding the body distribution (limited to e.g. liver and blood) of these contaminants and in relation to depuration via in ovo transfer. Maternal transfer rates and distribution were presently determined in six body compartments from eight female, Great Lakes herring gulls and separate egg compartments from their entire clutch. Among the 25 PBDEs and 23 non-PBDE HFRs assessed, only six PBDE congeners (BDE-47/99/100/153/154/209), hexabromocyclododecane (HBCDD), and Dechlorane Plus (syn- and anti-DDC-CO) were frequently detectable and quantifiable. Σ6BDE concentrations were an order of magnitude greater than non-PBDE HFR concentrations, and were greatest in the adipose (9641 ± 2436 ng/g ww), followed by egg yolk (699 ± 139 ng/g ww) > muscle (332 ± 545 ng/g ww) > liver (221 ± 65 ng/g ww) > plasma (85.4 ± 20.4 ng/g ww) > brain (54.6 ± 10.6 ng/g ww) > red blood cells (RBCs; 23.5 ± 5.6 ng/g ww) > albumen (7.3 ± 1.3 ng/g ww). Σ2DDC-CO and HBCDD were frequently below the method limit of quantification in the brain, RBCs, plasma, and albumen. Additionally, novel methoxylated-polybrominated diphenoxybenzene contaminants were detected and quantified in herring gull tissues and eggs. The primary difference in PBDE congener profiles was the resistance of both BDE-153 and -154 towards accumulation in the brain, and a corresponding increase in BDE-209 accumulation, which may suggest congener-specific differences in crossing the blood-brain barrier in herring gulls. Maternal transfer rates of PBDEs and non-PBDE HFRs were low (∼4.7 and ∼2.9 % respectively), suggesting that in ovo transfer is not a significant mode of depuration for these compounds.

Measuring exposure of e-waste dismantlers in Dhaka Bangladesh to organophosphate esters and halogenated flame retardants using silicone wristbands and T-shirts

Silicone (polydimethylsiloxane or PDMS) wristbands and cotton T-shirts were used to assess the exposure of e-waste recyclers in Dhaka, Bangladesh to polybrominated diphenyl ethers (PBDEs), novel brominated flame retardants (NBFRs), dechlorane plus (DPs), and organophosphate esters (OPEs). The median surface-normalized uptake rates of PBDEs, NBFRs, DPs, and OPEs were 170, 8.5, 4.8, and 270 ng/dm2/h for wristbands and 5.4, 2.0, 0.94, and 23 ng/dm2/h for T-shirts, respectively. Concentrations of Tris(2-chloroethyl) phosphate (TCEP), Tris(1,3-dichloro-2-propyl) phosphate (TDCIPP), Tri-m-cresyl phosphate (TmCP), Bis(2-ethlyhexyl) tetrabromophthalate (BEH-TEBP), and Dechlorane plus (DPs) in wristbands were significantly correlated with those in T-shirts. Wristbands accumulated ~7 times more mass than T-shirts, especially of compounds expected to be mainly in the gas phase. We introduce the silicone “sandwich” method to approximate the easily releasable fraction (ERF) from T-shirts, hypothesized to be related to dermal exposure. ERFs varied from 6 to 75% of total chemical accumulated by T-shirts and were significantly negatively correlated with compounds' octanol-air partition coefficient (log Koa). The median daily exposure doses via dermal transfer from the front of the T-shirt to the front body trunk were 0.32, 0.13, 0.11, and 9.1 ng/kg-BW/day for PBDEs, NBFRs, DPs, and OPEs, respectively. The evidence of e-waste recycler exposure to flame retardants in this low income country, lacking protective personal equipment, calls for measures to minimize their exposure and for chemical management regulations to consider exposures to chemicals in waste products.

Human exposure to legacy and emerging flame retardants in indoor dust: A multiple-exposure assessment of PBDEs

Human exposure to flame retardants (FRs) in indoor environments is a growing concern. In this study, the concentrations of polybrominated diphenyl ethers (PBDEs) and their alternatives, such as novel brominated flame retardants (NBFRs), dechlorane plus (DP), and organophosphate flame retardants (OPFRs), were measured in dust from indoor environments in Korea to investigate their occurrence, contamination profiles, and health risks. Legacy and emerging FRs were detected in dust samples, indicating widespread contamination of indoor environments. The concentrations of alternative FRs were higher in dust from offices compared with house dust, suggesting that office environments are major consumers of alternative FRs. Similar compositional profiles for indoor dust were found for PBDEs in different microenvironments and regions, while OPFR composition varied widely due to disparate applications. The estimated daily intakes of PBDEs, NBFRs, and OPFRs via dust ingestion were lower than the reference doses proposed by previous studies. A multiple-exposure assessment showed that dust ingestion was a major contributor to total PBDEs for toddlers and adults. However, major exposure pathways of BDEs 47 and 209 differed between toddlers and adults. Our study suggests that multiple exposure pathways should be considered in a comprehensive exposure assessment of PBDEs.

Polybrominated diphenyl ethers and alternative halogenated flame retardants in mangrove plants from Futian National Nature Reserve of Shenzhen City, South China

Halogenated flame retardants (HFRs) are ubiquitous in the environment, but little information is available about the bioaccumulation of HFRs in mangrove plants. In this study, three mangrove plant species were collected from Futian National Nature Reserve of Shenzhen City, South China to investigate the bioaccumulation of polybrominated diphenyl ethers (PBDEs) and several alternative halogenated flame retardants (AHFRs), including decabromodiphenyl ethane (DBDPE), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), hexabromobenzene (HBB), pentabromotoluene (PBT), tetrabromop-xylene (pTBX), pentabromoethylbenzene (PBEB) and dechlorane plus (DP). The mean concentrations of PBDEs, DBDPE, BTBPE, pTBX, PBT, PBEB, HBB and DP in mangrove plant species were 2010, 1870, 36.2, 18.7, 40.1, 17.8, 9.68 and 120 pg g−1 dry weight, respectively. PBDEs were the dominant HFRs in mangrove plant tissues, followed by DBDPE. The relative abundance of BDE 209 in three mangrove plant tissues were much lower than those in sediments. Significant negative relationships between log root bioaccumulation factors and log Kow, and between log TFr-s (from root to stem) and log Kow were observed, indicating that HFRs with low hydrophobicity were easily absorbed by mangrove roots and stems. A positive correlation between log TFs-l (from stem to leaf) and log Kow were found, suggesting that air-leaf exchange may occur in mangrove plants. This study highlights the uptake of HFRs by mangrove plants, which can be used as remediation for HFRs contamination in the environment.

Alternative halogenated flame retardants (AHFRs) in green mussels from the south China sea

Restrictions of legacy brominated flame retardants, such as polybrominated diphenyl ether (PBDE) and polybrominated biphenyl (PBB), have resulted in increased usage of alternative halogenated flame retardants (AHFRs). Consequently, AHFRs contamination has caused a major concern in the scientific community. However, there is limited information on their presence in marine mussels. In this study, we investigated the occurrence and distribution of polybrominated biphenyls (PBBs), AHFRs and dehalogenated products in green mussels collected from 22 locations in the northern South China Sea (SCS). Our results revealed that ∑AHFRs were ubiquitous in green mussels with concentrations in the range of 1.08–7.71 ng/g lipid weight (lw). Among target AHFRs, hexabromobenzene (HBB), decabromodiphenyl (DBDPE) and dechlorane plus (DP) were predominant with their mean values of 1.19, 1.00 and 0.82 ng/g lw, respectively. There were negligible stereoisomer enrichments of DP in green mussels based on fanti values, indicating a limited bioaccumulation and metabolism of DP in green mussels. In comparison with other locations, concentrations of the AHFRs in green mussels determined here were at moderate levels. Additionally, there were significant linear relationships between some AHFRs (e.g., HBB and PBEB), suggesting their similar commercial applications and sources in the environment. The estimated daily intakes of AHFRs through consumption of green mussels by the local population in South China were 0.05–0.14 ng/kg body weight/day and 0.17–0.44 ng/kg body weight/day based on the mean and 95th concentrations, respectively. To the best of our knowledge, the present study is the first to report AHFRs and dehalogenated products in green mussels.