Dechlorane Plus in air, dust, hand wipes, and hair at a typical e-waste site in South China: implications for human exposure.

Correlations between dechlorane plus concentrations in paired hair and indoor dust samples and differences between dechlorane plus isomer concentrations in hair from males and females

Dechlorane Plus (DP) in air and plants at an electronic waste (e-waste) site in South China

Dechlorane Plus in paired hair and serum samples from e-waste workers: Correlation and differences

Dechlorane Plus flame retardant in kingfishers (Alcedo atthis) from an electronic waste recycling site and a reference site, South China: Influence of residue levels on the isomeric composition

Sex-dependent accumulation and maternal transfer of Dechlorane Plus flame retardant in fish from an electronic waste recycling site in South China

It has been reported that breastfeeding can expose newborns to dechlorane plus (DP), but transplacental transfer of DP has not been documented. We measured DP and its dechlorinated analogs in matched maternal blood-placenta-cord blood samples from 72 residents of the e-waste recycling area of Wenling, China. DP was detected in cord sera, indicating the occurrence of prenatal DP exposure and the transfer of DP across the placenta. The concentration ratio in the cord serum and maternal serum was estimated to be 0.45 for syn-DP and 0.35 for anti-DP, indicating the placenta partially limited DP transfer with a greater extent for anti-DP. The DP concentrations in the maternal serum, placenta, and cord serum strongly correlated, indicating that DP could transfer between the tissues. The DP concentrations in the matched samples could be predicted from each other. The anti-DP/total DP concentration ratios in the placentas and cord sera were significantly different from those in the maternal sera, suggesting that DP stereoselectively bioaccumulates in human tissues. When the congener concentrations of polybrominated diphenyl ethers (PBDEs) were used as control variables, DP and total triiodothyronine concentrations were associated in the sera from mothers who had lived in Wenling for over 20 years.

Dechlorane Plus in serum from e-waste recycling workers: Influence of gender and potential isomer-specific metabolism

Legacy Dechlorane Plus in remediated electronic waste dismantling areas in East China: Multi-matrix exposure and isomer-specific bioaccumulation.

The occurrence and spatial distribution of dechloranes including mirex, dechlorane plus (DP), dechlorane (Dec) 602, Dec 603, and Dec 604 in surficial sediments of Lake Taihu were investigated in this study. The concentrations of mirex and DP ranged from below detection limit (BDL) to 1.29 ng g(-1) dw and 0.051 to 2.10 ng g(-1) dw, respectively. Dec 602, Dec 603, and Dec 604 on the other hand, were BDL in any of the samples. The contamination levels of DP were higher than that of Mirex at 21 of all 22 sampling sites. Levels of mirex and DP in the lake sediments were correlated when an extremely high mirex value was removed. Both mirex and DP levels were correlated with the amount of organic matters in the sediment samples. Spatial distribution of mirex and DP suggested that these two chemicals in the lake had similar input sources except for one site. Comparison to previously reported flame retardants' levels in the sediments shows that DP levels were similar with the levels of tetrabromobisphenol A, hexabromocyclododecane but lower than PBDEs and organophosphates levels in Lake Taihu. The higher levels in the north-east part of Lake Taihu adjacent to two major cities: Wuxi and Suzhou, indicated that city effluent might be a major source for DP contamination in the lake.

Dechlorane Plus (DP) is a high-production volume, chlorinated flame retardant comprising two major isomers, syn- and anti-DP. In this study, levels of DP were measured in soil and earthworm samples in farmland from a typical E-waste dismantling area in China. The concentrations of total DP ranged from 0.17 to 1,990ngg(-1)dw in soil samples and 3.43 to 89.2ngg(-1)lw in earthworm samples. Higher DP levels were found in some main E-waste dismantling sites than those in other sites. The ratios of anti-DP to total DP (f anti) ranged from 0.57 to 0.80 in soil samples and 0.47 to 0.81 in earthworm samples, respectively. The f anti in most samples in this study was in the range of the reported technical DP values. These results showed that improper E-waste dismantling activities could result in the emission of DP. Most earthworm samples showed very low BSAFs (biota-to-soil accumulation factors) for total DP. The values of BSAF were in the range of 0.0007-1.85, with an average value of 0.23. This study presents the first report of the DP in earthworms, which would be useful for ecological risk assessment of DP in terrestrial ecosystem.

The combined pollution of microplastics (MPs) and persistent organic pollutants (POPs) have attracted increasing attention from the international community in recent years. MPs can affect the toxicity, bioenrichment rate and bioavailability of POPs through adsorption and other interactions. Dechlorane Plus (DP) is a chlorinated flame retardant and a typical. DPs used mainly in various polymer materials, such as electrical wire and cable coating. The pollutions of MPs and DPs (syn and anti isomers, syn-DP [s-DP] and anti-DP [a-DP]) are ubiquitously present in the environment. However, the effect of MPs on the bioaccumulation of DP has not been reported. In this study, thick-shell mussels (Mytilus coruscus) were exposed to DPs (10 ng/L, DP10), DPs and polystyrene microplastics (PS) (10 ng/L DP +10 μg/L PS, DP10/PS10; 10 ng/LDP+20 μg/L PS, DP10/PS20) for 28 days to investigate the effect of MPs on DPs enrichment. Thick-shell mussels accumulated DPs in the adductor muscle, gill, and gonad showed an increasing trend with time, but the concentration of DPs in the visceral mass does not show a time-dependent manner. The concentration of DPs in the gonads and gills was significantly affected by the concentration of PS (p < 0.05), but there was no significant correlation between the concentration of DPs and the concentration of PS in the adductor muscle and visceral mass (p > 0.05). Moreover, DPs showed selective enrichment of syn-DP in thick-shell mussel tissues, and there was no significant correlation between this result and PS concentration (p > 0.05). These findings provide a new entry point for studying the interaction between microplastics and persistent organic pollutants in marine organisms.

Atmospheric concentrations of Dechlorane Plus (DP) were investigated in Taizhou, an electronic-waste (E-waste) dismantling region in East China. Passive air samplers with polyurethane foam (PUF) disks were deployed every three months during the sampling period of September 2009–August 2010. The total DP (syn- and anti-DP) concentrations in air ranged from not detected to 277 pg/m3, with a mean concentration of 53.9 pg/m3. A generally declining trend of DP levels was found from the E-waste dismantling region to the peripheral areas. The median values of total DP concentrations in autumn, winter, spring and summer were 52.2, 28.8, 39.7 and 30.1 pg/m3, respectively. The seasonal variations of DP concentrations were mainly associated with the intensity of E-waste dismantling activities and meteorological conditions. The mean value of anti-DP fractional abundance (f anti) was 0.74±0.08, which was consistent with those in the commercial DP products. This study confirmed a significant emission source related to the distribution of atmospheric DP in the E-waste dismantling area and supplied information for the seasonal variation of DP in the atmosphere.

Novel brominated flame retardants (NBFRs) and dechlorane plus (DP) have been widely used as alternatives to traditional BFRs. However, little is known about the temporal trends of NBFR and DP pollution in e-waste recycling sites. In the current study, three composite sediment cores were collected from an e-waste-polluted pond located in a typical e-waste recycling site in South China to investigate the historical occurrence and composition of NBFRs and DP. The NBFRs and DP were detected in all layers of the sediment cores with concentration ranges of 5.71~180,895 and 4.95~109,847 ng/g dw, respectively. Except for 2,3,5,6-tetrabromo-p-xylene (pTBX) and 2,3,4,5,6-pentabromoethylbenzene (PBEB), all the NBFR compounds and DP showed a clear increasing trend from the bottom to top layers. These results implied the long-term and severe contamination of NBFRs and DP. Decabromodiphenyl ethane (DBDPE) was the most abundant NBFR with the contribution proportions of 58 ± 15%, 73 ± 15%, and 71 ± 18% in three sediment cores, followed by 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE) and pentabromobenzene (HBB). The ratios of BTBPE/Octa-BDEs and DBDPE/Deca-BDEs varied from 0.12 to 60 and from 0.03 to 0.49, respectively, which had no clear increase trends with a decrease in sediment depth. As for DP, the fanti values (the concentration ratios of anti-DP to the sum of anti-DP and syn-DP) in sediment cores ranged from 0.41 to 0.83, almost falling in the range of those in DP technical products, suggesting that DP degradation did not occur in sediment cores. The environmental burdens of DBDPE, BTBPE, HBB, PBT, PBEB, pTBX, and DP were estimated to be 34.0, 5.67, 10.1, 0.02, 0.02, 0.01, and 34.8 kg, respectively. This work provides the first insight into the historical contamination status of NBFRs and DP in the sediments of an e-waste recycling site.

The highly chlorinated chemical Dechlorane Plus (DP) was introduced as a replacement flame retardant for Mirex, which is banned through the Stockholm Convention (SC) for its toxicity (T), environmental persistence (P), potential for bioaccumulation (B) and long-range environmental transport potential (LRETP). Currently, Dechlorane Plus is under consideration for listing under the Stockholm Convention and by the European Chemical Agency as it is suspected to also have potential for P, B, T and LRET. Knowledge of atmospheric concentrations of chemicals in background regions is vital to understand their persistence and long-range atmospheric transport but such knowledge is still limited for Dechlorane Plus. Also, knowledge on environmental occurrence of the less described Dechlorane Related Compounds (DRCs), with similar properties and uses as Dechlorane Plus, is limited. Hence, the main objective of this study was to carry out a spatial mapping of atmospheric concentrations of Dechlorane Plus and Dechlorane Related Compounds at background sites in Europe. Polyurethane foam passive air samplers were deployed at 99 sites across 33 European countries for 3 months in summer 2016 and analyzed for dechloranes. The study showed that syn- and anti-DP are present across the European continent (<MDL-2.6 pg/m3 and <MDL-12.3 pg/m3, respectively), including parts of the Arctic. This supports that these compounds have potential for long-range atmospheric transport to remote regions. The highest concentrations of Dechlorane Plus were observed in central continental Europe, with anti-DP fractions close to the commercial mixture of Dechlorane Plus. The only detected Dechlorane Related Compounds was Dechlorane-602, which was found in 27% of the samples (<MDL-0.33 pg/m3). The measured concentrations and spatial patterns of Dechlorane Plus and Dechlorane-602 in air across Europe indicate the influence of primary sources of these compounds on background concentrations in European air. Future air monitoring efforts targeting dechloranes is needed in both background and source areas, including consistent temporal trends.

Accumulation of Dechlorane Plus flame retardant in terrestrial passerines from a nature reserve in South China: The influences of biological and chemical variables