High Concentrations Of BDE-209 Research Articles

Contamination Status of Pet Cats in Thailand with Organohalogen Compounds (OHCs) and Their Hydroxylated and Methoxylated Derivatives and Estimation of Sources of Exposure to These Contaminants.

In this study, we analyzed serum samples of pet cats from Thailand and estimated the contribution to organohalogen compounds (OHCs) exposure through cat food and house dust intake. BDE-209 was predominant in cat sera and accounted for 76% of all polybrominated diphenyl ethers (PBDEs). Decabromodiphenyl ether (BDE-209) is a major contaminant in dry cat food and house dust, which has been estimated to be a source of exposure for Thai pet cats. BDE-209 is a major contaminant of OHCs in dry cat food and house dust, which was estimated to be a source of exposure for Thai pet cats. On the other hand, the level of contamination by PCBs was lower than in other countries. Analysis of pet foods suggested that BDE-209 in pet cat serum was attributable to the consumption of dry cat food. On the other hand, house dust also contained high concentrations of BDE-209. Thus, high levels of BDE-209 in pet cat sera can be attributed to the consumption of dry cat food and house dust. These results suggest that pet cats are routinely exposed to non-negligible levels of OHCs.

Occurrences and possible sources of persistent organic pollutants (POPs) in ice-free area soils in East Antarctica

Antarctica is widely regarded as a sink for persistent organic pollutants (POPs). However, there is a scarcity of data on the occurrence and spatial pattern of POPs in Antarctica, especially in the cold-xeric East Antarctica. Here, organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), and polybrominated diphenyl ethers (PBDEs) in soils from the Larsemann Hills, the second-largest ice-free area along East Antarctica, were investigated. It is shown that the main OCP contaminants were HCB, p,p’-DDD and δ-HCH (3.7–1522.3 pg g−1, 38.2–2276.6 pg g−1 and < LOD–570 pg g−1, respectively). OCPs in soils were primarily caused by long-distance atmospheric transport, but local sources can be found in areas heavily impacted by local human activities. Among DDTs and HCHs, only p,p’-DDD and δ-HCH were detected, indicating that DDTs and HCHs have aged. For PCBs (14.1–993.4 pg g−1), low-chlorinated PCB congeners were found in soil samples far from the station areas (Zhongshan, Progress II, and Progress I), possibly due to long-range atmospheric transport, while high levels of high-chlorinated PCB were found in the soils inside the station area (Law Base) and close to the main road, possibly associated with local station activities. Among the measured PBDEs (81.8–695.5 pg g−1), BDE-209 was the most frequently observed species, and the low-BDE found in soil samples could be from BDE-209 photodegradation. The majority of samples containing high concentrations of BDE-209 are concentrated in the station areas, implying that its source may be related to local station activities.

Pollution Status and Human Exposure of Decabromodiphenyl Ether (BDE-209) in China.

Decabromodiphenyl ether (BDE-209/decaBDE) is a high-production-volume brominated flame retardant in China, where the decaBDE commercial mixture is manufactured in Laizhou Bay, Shandong Province, even after the prohibition of penta- and octaBDE mixtures. The demand for flame retardants produced in China has been increasing in recent years as China not only produces electronic devices but also has numerous electronic waste (e-waste) recycling regions, which receive e-wastes from both domestic and foreign sources. High concentrations of BDE-209 have been observed in biotic and abiotic media in each of the different areas, especially within the decaBDE manufacturers and e-waste recycling areas. BDE-209 has been viewed as toxic and bioaccumulative because it might debrominate to less brominated polybrominated diphenyl ethers (PBDEs) (lower molecular weight and hydrophobicity), which are more readily absorbed by organisms. The highest concentration of PBDEs in dust within urban areas reached 40 236 ng g–1 in the Pearl River Delta, and BDE-209 contributed the greatest proportion to the total PBDEs (95.1%). Moreover, the maximum hazard quotient was found for toddlers (0.703) for BDE-209, which was close to 1. This suggests that exposure to BDE-209 might lead to increased potential for adverse effects and organ harm (e.g., the lungs) through inhalation, dust ingestion, and dermal absorption, especially for the group of toddlers compared to others. In daily food and human tissues, the amount of BDE-209 was also extensively detected. However, the toxicity and adverse effect of BDE-209 to humans are still not clear; thus, further studies are required to better assess the toxicological effects and exposure scenarios, a more enhanced environmental policy for ecological risks regarding BDE-209 and its debrominated byproducts in China.

Species- and Tissue-Specific Profiles of Polybrominated Diphenyl Ethers and Their Hydroxylated and Methoxylated Derivatives in Cats and Dogs.

The adverse effects of elevated polybrominated diphenyl ether (PBDE) levels, reported in the blood of domestic dogs and cats, are considered to be of great concern. However, the tissue distribution of PBDEs and their derivatives in these animals is poorly understood. This study determined the concentrations and profiles of PBDEs, hydroxylated PBDEs (OH-PBDEs), methoxylated PBDEs (MeO-PBDEs), and 2,4,6-tribromophenol (2,4,6-tri-BPh) in the blood, livers, bile, and brains of dogs and cats in Japan. Higher tissue concentrations of PBDEs were found in cats, with the dominant congener being BDE209. BDE207 was also predominant in cat tissues, indicating that BDE207 was formed via BDE209 debromination. BDE47 was the dominant congener in dog bile, implying a species-specific excretory capacity of the liver. OH-PBDE and MeO-PBDE concentrations were several orders of magnitude higher in cat tissues, with the dominant congener being 6OH-BDE47, possibly owing to their intake of naturally occurring MeO-PBDEs in food, MeO-PBDE demethylation in the liver, and lack of UDP-glucuronosyltransferase, UGT1A6. Relatively high concentrations of BDE209, BDE207, 6OH-BDE47, 2'MeO-BDE68, and 2,4,6-tri-BPh were found in cat brains, suggesting a passage through the blood-brain barrier. Thus, cats in Japan might be at a high risk from PBDEs and their derivatives, particularly BDE209 and 6OH-BDE47.

Occurrence and Concentrations of Halogenated Flame Retardants in the Atmospheric Fine Particles in Chinese Cities.

The concentrations of halogenated flame retardants (HFRs) in PM2.5 were monitored for one year at 10 urban sites in China during 2013-2014. This study investigated four classes of HFRs: nine polybrominated diphenyl ethers (PBDEs), six nonbromodiphenyl ether (BDE) brominated flame retardants, two dechlorane plus (DP) flame retardants, and three chlorinated organophosphate flame retardants (OPFRs). Extremely high concentrations of BDE-209 and DBDPE were observed in only one city (Guangzhou), which was a consequence of the intensive e-waste recycling and disposal operations in the Pearl River Delta. This result differed from the tris(monochloropropyl) phosphate (TCPP) and tris(2-chloroethyl) phosphate (TCEP) distributions, which showed high concentrations in most cities, suggesting wide usage and large emissions in China in recent years. The highest TCPP and TCEP concentrations were observed in the summer, indicating that emission from local sources was an important factor controlling the levels in the air. This was not the case for BDE-209 and DBDPE, for which higher concentrations were found in winter. When bound to particulate matter due to low vapor pressure, these compounds may be more persistent in air, and temperature-dependent gas-particle partitioning was a key factor. Moreover, regional pollution and long-range transport had a significant influence on the seasonal distributions of BDE-209 and DBDPE, especially in cities (Guangzhou and Shanghai) close to electrical/electronic waste recycling sites. Residents in urban areas were exposed to higher levels of chlorinated OPFRs. This raises considerable concern, and an appropriate risk assessment is required.

Wide range of metallic and organic contaminants in various tissues of the Antarctic prion, a planktonophagous seabird from the Southern Ocean

Trace elements (n=14) and persistent organic pollutants (POPs, n=30) were measured in blood, liver, kidney, muscle and feathers of 10 Antarctic prions (Pachyptila desolata) from Kerguelen Islands, southern Indian Ocean, in order to assess their concentrations, tissue distribution, and inter-tissue and inter-contaminant relationships. Liver, kidney and feathers presented the highest burdens of arsenic, cadmium and mercury, respectively. Concentrations of cadmium, copper, iron, and zinc correlated in liver and muscle, suggesting that uptake and pathways of metabolism and storage were similar for these elements. The major POPs were 4,4'-DDE, mirex, PCB-153 and PCB-138. The concentrations and tissue distribution patterns of environmental contaminants were overall in accordance with previous results in other seabirds. Conversely, some Antarctic prions showed surprisingly high concentrations of BDE-209. This compound has been rarely observed in seabirds before, and its presence in Antarctic prions could be due to the species feeding habits or to the ingestion of plastic debris. Overall, the study shows that relatively lower trophic level seabirds (zooplankton-eaters) breeding in the remote southern Indian Ocean are exposed to a wide range of environmental contaminants, in particular cadmium, selenium and some emerging-POPs, which merits further toxicological investigations.

Fingerprint analysis of brominated flame retardants and Dechloranes in North Sea sediments

53 brominated and chlorinated flame retardants were investigated in sediment samples from the German rivers Elbe and Weser, the German Bight, Jadebusen, East Frisian Coast as well as the UK East coast. The aim of the presented study was to investigate the prevalence of different halogenated flame retardant groups as contaminants in North Sea sediments, identify determining factors for the distribution and levels as well as to identify area specific fingerprints that could help identify sources.In order to do that a fast and effective ASE extraction method with an on-line clean-up was developed as well as a GC-EI-MSMS and LC-ESI-MSMS method to analyse PBDEs, MeOBDEs, alternate BFRs, Dechloranes as well as TBBPA and HBCDD. A fingerprinting method was adopted to identify representative area-specific patterns based on detection frequency as well as concentrations of individual compounds. Concentrations in general were low, with<1ngg−1dw for most compounds. Exceptions were the comparably high concentrations of BDE-209 with up to 7ngg−1dw in selected samples and TBBPA in UK samples with 2.7±1.5ngg−1dw. Apart from BDE-209 and TBBPA, alternate BFRs and Dechloranes were predominant in all analysed samples, displaying the increasing relevance of these compounds as environmental contaminants.

The influence of land use on the concentration and vertical distribution of PBDEs in soils of an e-waste recycling region of South China

The vertical distribution of polybrominated diphenyl ethers (PBDEs) in soil at four sites within an e-waste recycling region of South China was investigated. PBDE concentrations in soil ranged from 1.38 to 765 ng/g. There was a trend of decreasing PBDE concentration with soil depth, especially in the paddy field. However, high concentrations of BDE-209 were found in deeper soils indicating a highly preferential migration. There was a stronger correlation between PBDEs and total organic carbon (TOC), compared to dissolved organic carbon (DOC), which suggests that the association between non-dissolved organic carbon (NDOC) and PBDEs is stronger than for DOC. Different land use types, in particular differences in farming activities, significantly influenced the vertical distribution of PBDEs in soils. PBDEs displayed a higher leaching tendency in moist paddy soil than in drier soils. The frequent flooding condition in paddy field may facilitate the vertical transfer of PBDEs to the deeper soils.

Debrominated and methoxylated polybrominated diphenyl ether metabolites in rainbow trout ( Oncorhynchus mykiss) after exposure to decabromodiphenyl ether

Abstract Decabromodiphenyl ether (BDE209) is the primary component in a commonly used flame retardant. Previous studies had proved that BDE209 itself was not toxic, while its metabolites including debrominated diphenyl ethers (De-BDEs) and methoxylated brominated diphenyl ethers (MeO-BDEs) posed a potential threat to organisms. Many studies had indicated that BDE209 could metabolize quickly in mammals, but lacking in the basic data about the metabolism of BDE209 in fish. In the present study, two replicate treatment groups of rainbow trout ( Oncorhynchus mykiss) were exposed to BDE209 via a single intraperitoneal injection approximately 100 and 500 ng/g, respectively. Muscle, liver and blood samples were collected to analyze the specific metabolites on day 1 and day 28 post injection. The highest concentration of BDE209 was detected in muscle tissues, from 796.1 ng/g wet weight (day 1) to 687.1 ng/g wet weight (day 28) in high dose group, suggesting that BDE209 could accumulate slightly in muscle tissues. However, BDE209 was not detected in the blood for all treatments. Most congeners of De-BDEs were found in muscle and liver tissues, with the highest concentration in the liver. The main De-BDEs were nona-, octa-, hepta- and penta-De-BDEs. A total of seven MeO-BDE metabolites were observed among different fish tissues. Blood had the highest contribution of the MeO-BDE metabolites. Each MeO-BDE congener increased over the 28 days. These results in contrast to other studies suggested possible species-specific differences in metabolic abilities.

Bioaccumulation and biomagnification of polybrominated diphenyl ethers in a food web of Lake Michigan

Polybrominated diphenyl ethers are hydrophobic chemicals and can biomagnify in food chains. Little is known about the biomagnification of PBDEs in the Lake Michigan food web. Plankton, Diporeia, lake whitefish, lake trout, and Chinook salmon were collected from Lake Michigan in 2006 between April and August. Fish liver and muscle and whole invertebrates were analyzed for six PBDEs (BDE-47, 99, 100, 153, 154, and 209). Carbon and nitrogen stable isotope ratios (delta(13)C and delta(15)N) were also quantified in order to establish the trophic structure of the food web. Geometric means of Sigma PBDE concentrations in fish ranged from 0.562 to 1.61 microg/g-lipid. BDE-209 concentrations ranged from 0.184 to 1.23 microg/g-lipid in all three fish species. Sigma BDE-47, 99, and 209 comprised 80-94% of Sigma PBDE molar concentration. Within each fish species, there were no significant differences in PBDE concentrations between liver and muscle. The highest concentration of BDE-209 (144 microg/g-lipid) was detected in Diporeia. Based on analysis of delta(15)N and PBDE concentrations, BDE-47 and 100 were found to biomagnify, whereas BDE-209 did not. A significant negative correlation between BDE-209 and trophic level was found in this food web. Biomagnification factors were also calculated and again BDE-47 and 100 biomagnified between food web members whereas BDE-209 did not. Diporeia could be one of the main dietary sources of BDE-209 for fish in Lake Michigan; BDE-47 and 100 biomagnified within this food chain; the concentration of BDE-209 decreased at higher trophic levels, suggesting partial uptake and/or biotransformation of BDE-209 in the Lake Michigan food web.

Flame Retardants in the Atmosphere near the Great Lakes

As part of the Integrated Atmospheric Deposition Network (IADN), air samples were collected at five sites around the Great Lakes (two urban, two rural, and one remote) every 12 days during 2005-2006, and the concentrations of polybrominated diphenylethers (PBDEs), 1,2-bis(2,4,6-tribromophenoxy)-ethane (TBE), Dechlorane Plus (DP), and decabromodiphenyl ethane (DBD PE) were measured. The highest mean concentrations of total PBDEs were found at the urban sites in Chicago and Cleveland (65 +/- 4 and 87 +/- 8 pg/m3, respectively), and the lowest at the remote site in Eagle Harbor (5.8 +/- 0.4 pg/m3). With the exception of Chicago, the atmospheric concentrations of BDE-47 and 99 (summed over the gas and particle phases) are decreasing rapidly with half-lives of approximately 2 years, but the concentrations of BDE-209 are not decreasing at any of the five sites. The atmospheric partial pressures of BDE-47 and 99 showed a strong Clausius-Clapeyron relationship with reciprocal atmospheric temperature. TBE, DBDPE and DP were detected at all sites, but with the exception of Chicago, there were insufficient data to determine temporal trends for these compounds. The influence of human population density and synoptic atmospheric transport patterns was explored to explain the relatively high concentrations of BDE-209 in Cleveland.

Exposure to polybrominated diphenyl ethers among workers at an electronic waste dismantling region in Guangdong, China

Polybrominated diphenyl ethers (PBDEs) are widely used as flame retardants. The aim of the present study was to evaluate the PBDE serum levels in residents from an electronic waste dismantling region, residents living within 50 km of the dismantling region, and a referent group with no occupational PBDE exposure. Fourteen PBDE congeners including BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154, BDE-183, BDE-196, BDE-197, BDE-203, BDE-206, BDE-207, BDE-208 and BDE-209 were quantified in these three groups by gas chromatography–negative chemical ionization (NCI) mass spectrometry in selected ion monitoring (SIM) mode. We found that the levels of all PBDE congeners in serum of residents from electronic waste dismantling region were significantly higher than those in the two other groups. The referents showed the lowest PBDE levels. Concentrations of congeners with a high number of bromine substituents, i.e., hepta- to decaBDEs in occupational exposure workers were 11–20 times higher than those in the referent group. BDE-209 was the dominant congener. The highest concentration of BDE-209 was observed among the electronic waste dismantling workers, and it was 3436 ng g−1 lipid weight (ng g−1 l.w.), which is the highest concentration of BDE-209 in humans worldwide. Some higher brominated PBDE congeners such as BDE-197, BDE-207 and BDE-208 also showed elevated concentrations in dismantling workers. This study confirms that BDE-209 is released to the environment and can bioaccumulate in the blood of electronic waste dismantling workers, and extensive occupational exposure to PBDEs leads to elevated concentrations of all PBDE congeners in serum.

Flame retardants, surfactants and organotins in sediment and mysid shrimp of the Scheldt estuary (The Netherlands)

Sediment and mysids from the Scheldt estuary, one of the largest and most polluted estuaries in Western Europe, were analyzed for a number of contaminants that have been shown to possess endocrine-disrupting activity, i.e. organotins, polybrominated diphenyl ethers (PBDEs), hexabromocyclododecane (HBCD), tetrabromobisphenol A (TBBPA), nonylphenol ethoxylates (NPE) and transformation products, nonylphenol (NP) and nonylphenol ether carboxylates (NPEC). In addition, in vitro estrogenic and androgenic potencies of water and sediment extracts were determined. Total organotin concentrations ranged from 84 to 348 ng/g dw in sediment and 1110 to 1370 ng/g dw in mysid. Total PBDE (excluding BDE-209) concentrations ranged from 14 to 22 ng/g dw in sediment and from 1765 to 2962 ng/g lipid in mysid. High concentrations of BDE-209 (240–1650 ng/g dw) were detected in sediment and mysid (269–600 ng/g lipid). Total HBCD concentrations in sediment and mysid were 14–71 ng/g dw and 562–727 ng/g lipid, respectively. Total NPE concentrations in sediment were 1422 ng/g dw, 1222 ng/g dw for NP and 80 ng/g dw for NPEC and ranged from 430 to 1119 ng/g dw for total NPE and from 206 to 435 ng/g dw for NP in mysid. Significant estrogenic potency, as analyzed using the yeast estrogen assay, was detected in sediment and water samples from the Scheldt estuary, but no androgenic activity was found. This study is the first to report high levels of endocrine disruptors in estuarine mysids.