Organochlorines in Greenland glaucous gulls (Larus hyperboreus) and Icelandic gulls (Larus glaucoides)

Glaucous gulls (Larus hyperboreus) and Icelandic gulls (Larus glaucoides) were sampled in 1994 from four different areas in Greenland, three on the west coast and one on the east coast. Livers of 93 glaucous gulls and seven Icelandic gulls were analysed for polychlorinated biphenyls (PCBs, IUPAC Nos. 28, 31, 52, 101, 105, 118, 138, 153, 156 and 180), DDTs (p,p'-DDE, p,p'-DDD, p,p'-DDT), hexachlorocyclohexanes (alpha-, beta- and gamma-HCH), hexachlorobenzene (HCB) and trans-nonachlor (TNC). The overall geometric means of the concentrations found in glaucous gull liver were for sigma PCBs 388 (range 20-5557), for sigma DDTs 363 (17-8604), sigma HCHs 7.4 (1-53), HCB 47 (4-594) and trans-nonachlor 19 (3-187) micrograms kg-1 wet wt., respectively. The geometric means of concentrations in Icelandic gull liver were for sigma PCBs 112 (24-435), for sigma DDTs 95 (25-298), sigma HCHs 2.9 (1.4-5.2), HCB 22 (8-58) and trans-nonachlor 5.1 (2.4-8.6) micrograms kg-1 wet wt., respectively. Significantly (P = 0.05) higher concentrations of PCBs, DDTs and HCHs were found in glaucous gulls at Ittoqqortoormiit at the east coast than in gulls from Qeqertarsuaq at the west coast of Greenland. This tendency was also seen for HCB and trans-nonachlor, but the differences were not statistically significant (P = 0.05). A decreasing trend in organochlorine concentrations followed the East Greenland Current, flowing from north to south down the east coast and to the north on the west coast. Gulls taken from the most northerly sampling area of the west coast, however, showed slightly higher concentrations than those from the central west coast. There appeared to be a tendency for higher concentrations to be found in males than females, and in adults compared to young glaucous gulls, but the differences were not statistically significant (P = 0.05). The concentration ranges found in gulls from Greenland were similar to those reported previously for gulls from northern Norway and Russia. A principal component analysis revealed no obvious link between the presence of higher chlorinated PCBs and higher PCB concentrations in glaucous gulls. Significantly higher proportions of higher chlorinated PCBs were found in glaucous gulls than in Icelandic gulls, and in adult glaucous gulls compared to young gulls of 1-2 calendar years. As no such difference was found between female and male gulls it seems that PCBs of all degrees of chlorination may be passed equally well from mother to offspring.     

The use of blue tit eggs as a biomonitoring tool for organohalogenated pollutants in the European environment

In the present study, large scale geographical variation in the occurrence of organohalogenated pollutants (OHPs) was investigated throughout Europe using eggs of a terrestrial resident passerine species, the blue tit (Cyanistes caeruleus). Blue tit eggs from 10 sampling locations, involving suburban, rural and remote areas, in 7 European countries were collected and analysed. Sum polychlorinated biphenyl (PCB) levels ranged from 150 ng/g lipid weight (lw) to 2003 ng/g lw. Sum polybrominated diphenyl ethers (PBDEs) ranged from 3.95 ng/g lw to 114 ng/g lw. As expected, PCB and PBDE concentrations were significantly higher in the sampled suburban locations compared to the rural and remote locations. Sum organochlorine pesticides (OCPs) ranged from 122 ng/g lw to 775 ng/g lw. OCP concentrations were, against the expectations, found to be lower in the rural sampling locations compared to the other locations. Contamination profiles of PCBs, PBDEs and OCPs differed also among the sampling locations, which may be due to local contamination sources. Finally, we compared the results of this study with previously reported OHP concentrations in the eggs of a closely related species, the great tit (Parus major), from the same sampling locations in Europe. We found no differences in concentrations between the species. In addition, we found a significant, positive correlation between the sum PCB concentrations in blue tit eggs and great tit eggs, suggesting similar exposure pathways, mechanisms of accumulation and maternal transfer of PCBs. In conclusion, our results suggest the usefulness of eggs from passerine birds as a biomonitoring tool for OHPs on a large geographical scale.     

Burdens of PBBs, PBDEs, and PCBs in tissues of the cancer patients in the e-waste disassembly sites in Zhejiang, China

This study was conducted to explore the burdens of PBBs, PBDEs, and PCBs among cancer patients living in the e-waste disassembly sites. The contents of 23 PBB congeners, 12 PBDE congeners, and 27 PCB congeners in kidney, liver, and lung samples were measured by GC-MS. The results showed that low-brominated PBBs and PBB153 were the predominant congeners. PBDE47 were the most predominant PBDE congeners. PBDE209 were detected in > 70% of the samples, with geometric means ranging from 64.2 to 113.9 ng g^− 1 lipid. Among the three subfamilies of PHAHs, PCB concentrations were the highest. The detected levels of PHAHs were in the same order of magnitude in the three tissues, which indicated that any of the three tissues could be the suitable indicator for assessing body burdens of PHAHs. PBB contents (181-192 ng g^− 1 lipid) were obviously higher than those reported in the general USA population (3-8 ng g^− 1 lipid). PBDE levels (174.1-182.3 ng g^− 1 lipid) were comparable to those reported in the USA population, but significantly higher than those of the European population. PCBs levels were comparable to those of the European population. The high cancer incidence in the disassembly sites may be related to higher burdens of PBBs, PBDEs, and PCBs in tissues.     

Bioaccumulation behaviour of polybrominated diphenyl ethers (PBDEs) in a Canadian Arctic marine food web

A comparative analysis of the bioaccumulation behaviour of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) was conducted involving simultaneous measurements of PBDE and PCB concentrations in organisms of a Canadian Arctic marine food web. Concentrations of individual PBDE congeners (BDE-28, -47, -99, -153, -154 and -183) in Arctic marine sediments (0.001-0.5 ng.g(-1) dry wt) and biota (0.1-30 ng.g(-1) wet wt) were low compared to those concentrations in biota from urbanized/industrial regions. While recalcitrant PCB congeners exhibited a high degree of biomagnification in this food web, PBDE congeners exhibited negligible biomagnification. Trophic magnification factors (TMFs) of PCBs ranged between 2.9 and 11, while TMFs of PBDEs ranged between 0.7 and 1.6. TMFs of several PBDE congeners (BDE-28, -66, -99, -100, -118, -153 and -154) were not statistically greater than 1, indicating a lack of food web magnification. BDE-47 was the only PBDE with a TMF (i.e. 1.6) statistically greater than 1, hence showing evidence of biomagnification in the food web. However, the TMF of BDE-47 (1.6) was substantially lower than TMFs of recalcitrant Cl(5)-Cl(7) PCBs (TMFs~9-11). Species-specific bioaccumulation factors (BAFs) of PBDEs in homeotherms were much smaller than those for PCBs. This further indicates the low degree or absence of biomagnification of PBDEs compared to PCBs in this food web. The field observations suggest PBDEs exhibit a relatively rapid rate of depuration though biotransformation in Arctic marine organisms, which is consistent with laboratory studies in fish and rats.     

Contaminant blubber burdens in Atlantic bottlenose dolphins (Tursiops truncatus) from two southeastern US estuarine areas: Concentrations and patterns of PCBs, pesticides, PBDEs, PFCs, and PAHs

Polychlorinated biphenyls (PCBs), chlorinated pesticides (i.e., dichlorodiphenyltrichloroethane (DDT) and its metabolites, chlordanes (CHLs), dieldrin, hexachlorobenzene (HCB), and mirex), polybrominated diphenyl ethers (PBDEs), perfluorinated chemicals (PFCs), and polyaromatic hydrocarbons (PAHs) were measured in blubber biopsy samples collected from 139 wild bottlenose dolphins (Tursiops truncatus) during 2003-2005 in Charleston (CHS), SC and the Indian River Lagoon (IRL), FL. Dolphins accumulated a similar suite of contaminants with ∑ PCB dominating (CHS 64%, IRL 72%), followed by ∑ DDT (CHS 20%, IRL 17%), ∑ CHLs (CHS 7%; IRL 7%), ∑ PBDE (CHS 4%, IRL 2%), PAH at 2%, and dieldrin, PFCs and mirex each 1% or less. Together ∑ PCB and ∑ DDT concentrations contributed ∼ 87% of the total POCs measured in blubber of adult males. ∑ PCBs in adult male dolphins exceed the established PCB threshold of 17 mg/kg by a 5-fold order of magnitude with a 15-fold increase for many animals; 88% of the dolphins exceed this threshold. For male dolphins, CHS (93,980 ng/g lipid) had a higher ∑ PCBs geomean compared to the IRL (79,752 ng/g lipid) although not statistically different. In adult males, the PBDE geometric mean concentration was significantly higher in CHS (5920 ng/g lipid) than the IRL (1487 ng/g). Blubber ∑ PFCs concentrations were significantly higher in CHS dolphins. In addition to differences in concentration of PCB congeners, ∑ PBDE, TEQ, ∑ CHLs, mirex, dieldrin, and the ratios ∑ DDE/∑DDT and trans-nonachlor/cis-nonachlor were the most informative for discriminating contaminant loads in these two dolphin populations. Collectively, the current ∑ PCB, ∑ DDT, and ∑ PBDEs blubber concentrations found in CHS dolphins are among the highest reported values in marine mammals. Both dolphin populations, particularly those in CHS, carry a suite of organic chemicals at or above the level where adverse effects have been reported in wildlife, humans, and laboratory animals warranting further examination of the potential adverse effects of these exposures.     

Polybrominated diphenyl ethers and polychlorinated biphenyls in indoor dust in Durban,South Africa

Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were measured in indoor dust of three microenvironments in Durban, South Africa. The sum of eight PBDEs and three PCBs were quantified by gas chromatography with mass spectral detection. The mean concentrations of ∑_n = 8 PBDEs and ∑_n = 3 PCBs in 10 homes, 11 offices, and 13 university students’ computer laboratories were 1710, 1520, and 818 ng/g, and 891, 923, and 1880 ng/g for PBDEs and PCBs, respectively. The concentration of PCBs found in homes was independent (P = 0.0625) of building construction year. Similarly, no relationship was observed between PCB concentrations and floor type. The concentrations of PBDEs correlated (r = 0.60) with PCB concentrations in homes, thus assuming similar sources. The elevated concentrations of PBDEs and PCBs may have significant implications for human exposure.     

The status of soil contamination by semivolatile organic chemicals (SVOCs) in China: a review

This paper summarizes the published scientific data on the soil contamination by semivolatile organic chemicals (SVOCs) in China. Data has been found for more than 150 organic compounds which were grouped into six classes, namely, polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs) and phthalic acid esters (PAEs). An overview of data collected from the literature is presented in this paper. The Chinese regulation and/or other maximum acceptable values for SVOCs were used for the characterization of soils. In general, the compounds that are mostly studied in Chinese soils are OCPs, PAHs and PCBs. According to the studies reviewed here, the most abundant compounds were PAEs and PAHs (up to 46 and 28 mg kg(-1) dry weight, respectively); PCBs and OCPs occurred generally at concentrations lower than 100 microg kg(-1) dry weight. Nevertheless, quite high concentrations of PCDD/Fs, PCBs and PBDEs were observed in contaminated sites (e.g., the sites affected by electronic waste activities). The average concentrations of PAHs and OCPs in soils of North China were higher than those in South China. The principal component analysis demonstrated different distribution patterns for PAH, PCB and PCDD/F congeners and for the various sites/regions examined. The isomer ratios of DDTs and hexachlorocyclohexanes (HCHs) indicated different sources and residue levels in soils. Finally, this review has highlighted several areas where further research is considered necessary.     

Organochlorine pesticide, polychlorinated biphenyl and heavy metal concentrations in wolves (Canis lupus L. 1758) from north-west Russia

The wolf Canis lupus is a major terrestrial predator in eastern Europe and, as a top carnivore, may be exposed to high concentrations of contaminants that are readily transferred through the food chain. Despite this, there are few published data on pollutant and pesticide levels in wolves. This study utilised tissues from animals legally killed by hunters for other reasons (animals were not killed for the purposes of this study) to carry out the only detailed investigation of contaminants in wolves in Europe and the first in animals from Eastern Europe. The livers of 58 wolves from the Tver and Smoliensk regions of northwest Russia (54°N 31°E to 57°N 35°E) were analysed for seven organochlorine pesticides, 24 PCB congeners, Aroclor 1254-matched summed PCBs (ΣPCBs), total mercury, cadmium and lead. Cadmium, most of the organochlorine pesticides and many PCB congeners were not detectable in any of the wolves. Hexachlorobenzene, alpha-HCH, pp′DDE, PCB congeners 118, 138, 149 and 156 and lead were detected in up to 6% of livers. Dieldrin, PCB congeners 153, 170 and 180, ΣPCBs and mercury were detected more frequently. Contaminant levels were generally low; maximum wet weight concentrations of any of the organochlorine pesticides, ΣPCBs and mercury were less than 0.1, 1 and 0.25 μg g⁻¹, respectively. PCB congeners 153, 170 and 180 accounted for 41% of the ΣPCBs. Dieldrin, ΣPCBs and mercury concentrations did not vary significantly between males and females nor between adult and juvenile (<12 months old) wolves apart from the ΣPCB concentration, which was on average five times higher in adults than juveniles. Liver residues were generally below the level normally associated with adverse effects except for lead levels which exceeded the critical 5 μg g⁻¹ dry wt. concentration in three of the 58 animals examined.     

Brominated flame retardants in the Arctic environment — trends and new candidates

Polybrominated diphenyl ethers (PBDEs) containing two to 10 bromines are ubiquitous in the Arctic, in both abiotic and biotic samples. Hexabromocyclododecane (HBCD) is also ubiquitous in the Arctic, with the γ-HBCD isomer predominating in air, the α-HBCD isomer predominating in biota and similar concentrations of α-, β- and γ-HBCD found in marine sediments. Other brominated flame retardants (BFRs) found in some Arctic samples are polybrominated biphenyls (PBBs), tetrabromobisphenol A (TBBPA), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), hexabromobenzene (HxBBz), pentabromoethylbenzene (PBEB), pentabromotoluene (PBT), and 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane (TBECH). Temporal trends of tetra- to heptaBDEs and HBCD show increasing concentrations or a tendency to levelling off depending on the matrix (air, sediment, biota) and location, but no uniform picture for the Arctic emerges. BDE-209 concentrations are increasing in air. PBDEs and HBCD spatial trends in seabirds and marine mammals are similar to those seen previously for polychlorinated biphenyls (PCBs), with highest concentrations found in organisms from East Greenland and Svalbard. These trends indicate western Europe and eastern North America as important source regions of these compounds via long range atmospheric transport and ocean currents. Latitudinal trends showed lower concentrations and fluxes of PBDEs at higher latitudes. The tetra-hexaBDEs and α-HBCD biomagnify in Arctic food webs. Results for BDE-209 are more conflicting, showing either only low or no biomagnification potential. PBDE and HBCD concentrations are lower in terrestrial organisms and higher in marine top predators such as some killer whale populations in Alaska and glaucous gulls from the Barents Sea area. Higher concentrations are seen near populated areas indicating local sources. Findings of BTBPE, HxBBz, PBEB, PBT and TBECH in seabirds and/or marine mammals indicate that these compounds reach the Arctic, most probably by long range atmospheric transport and accumulate in higher trophic level organisms and that increasing use as PBDE replacements will lead to increasing concentrations.     

Concentrations of polybrominated diphenyl ethers, polychlorinated dibenzo-p-dioxins and dibenzofurans, and polychlorinated biphenyls in human blood samples from Korea

Analysis of blood samples is an effective way of evaluating contamination by persistent pollutants such as polybrominated diphenyl ethers (PBDEs), polychlorinated dibenzo-p-dioxin/furans (PCDD/Fs), and polychlorinated biphenyls (PCBs) in human population. Concentrations of PBDEs, PCDD/Fs and PCBs were measured in the blood of laborers (n = 13) working full time in two different municipal waste incinerator (MWI) plants and residents from the general population (n = 22) living in areas near MWIs in Korea. The concentrations of PBDEs were found to be slightly higher in the blood of incineration workers (8.61-46.05 ng/g lipid; mean, 19.33 ng/g lipid; median, 15.94 ng/g lipid) in comparison to that of residents from the general population (7.24-28.89 ng/g lipid; mean, 15.06 ng/g lipid; median, 14.34 ng/g lipid). The total average PCDD/Fs and PCB TEQ concentration was 20.11 pg/g lipid, averaged over incineration workers (17.73 pg/g lipid) and the general population (21.52 pg/g lipid). In addition, the average total crude concentration of PCDD/Fs was 7.40 ng/g lipids, which was 4.1 times greater than for PBDEs. Congener specific analysis confirmed that BDE 47 was a predictive indicator for total PBDE concentration (correlation coefficient r = 0.912), and that PCB 153 was a predictive indicator for total PCB concentration (r = 0.967). The PBDE levels in human blood in Korea are much higher than those reported in other countries. The presence of the BDE 183 congener was characteristic in the blood of workers from an electronic dismantling facility in MWIs.     

Biomagnification of PBDEs and PCBs in food webs from the Baltic Sea and the northern Atlantic Ocean

Biomagnification of polychlorinated biphenyls (PCBs) and polybrominated diphenylethers (PBDEs) in food webs from the Baltic Sea and the northern Atlantic Sea was investigated. For this, we used PCB and PBDE concentration data, together with data on fish body weight and delta15N of fish and zooplankton as a measure of trophic position. In the Baltic Sea material, consisting of zooplankton, sprat, herring and salmon, we report biomagnification of all PCB congeners but PCB #209 and of PBDEs with 3-6 or 7 bromine atoms. Higher brominated PBDEs and PCB 209 did not biomagnify likely due to their high molecular weights or sizes and subsequent inefficient dietary uptake in fish. If salmon was excluded from the statistical analysis, strong biomagnification of PCB #209 was evident, indicating species differences in biomagnification. In the Baltic Sea material delta15N and body weight covaried. In the Atlantic Sea material, consisting of fish samples (herring and salmon) of larger body sizes, we show positive correlation between concentrations of most PCBs and PBDEs and body weight without increasing delta15N. This shows that biomagnification in some cases depends on body size and not trophic position. We conclude that there probably is trophic position dependence in biomagnification, which was manifested in a food chain from zooplankton to piscivores, but no further trophic position influence on biomagnification in fish at the highest trophic levels. In these fish, there was a body size effect leading to biomagnification, probably due to slower clearance in larger fish. PCB concentrations were generally between 2 and 6 times higher in Baltic Sea salmon than in Atlantic Sea salmon. Higher PBDE concentrations in the Baltic compared to the Atlantic Sea salmon were also found, but with a larger variation between congeners. Nona- to deca-BDEs were found in most investigated samples, which illustrates the bioavailability of these compounds. Unidentified penta-, hexa-, hepta-, and octa- BDEs were found in several samples.     

Levels, fluxes and time trends of persistent organic pollutants in Lake Thun, Switzerland: Combining trace analysis and multimedia modeling

Levels, mass fluxes, and time trends of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) in Lake Thun, a peri-Alpine lake, are investigated. We present measurements of PBDEs and PCBs in air, lake water, lake sediment, and tributary water. These measurements are combined with a multimedia fate model, based on site-specific environmental parameters from the lake catchment. Measured loadings of PBDEs and PCBs in air and tributaries were used to drive the model. The model satisfactorily reproduces PBDE and PCB congener patterns in water and sediment, but it tends to yield concentrations in water below the measurements and concentrations in sediment exceeding the measurements. A sensitivity analysis reveals that partitioning of PBDEs and PCBs between the aqueous dissolved phase and suspended particulate matter in the water column strongly affects the model results, in particular the concentrations in water and sediment. For lower-brominated PBDEs, approximately 70% and 30% of input into the lake stems from atmospheric deposition and from tributaries, respectively. For heavier PBDEs and all PCBs, rivers appear to deliver the major load (64-92%). Waste water effluents are of minor importance. 50-90% of the total input is buried in the permanent sediment. Sediment burial makes PBDEs and PCBs less available for recycling in the environment, and reduces concentrations in the outflowing river. If use of deca-BDE increases in the future, levels in Lake Thun will follow the same trend. If the use and resulting environmental emissions decrease, concentrations in water will rapidly decline, according to our calculations, while sediment levels will decrease at a considerably slower rate.     

PCB dechlorination enhancement in Anacostia River sediment microcosms

In situ treatment of PCB contaminated sediments via microbial dechlorination is a promising alternative to dredging, which may be reserved for only the most contaminated areas. Reductive dechlorination of low levels of weathered PCB mixtures typical of urban environments may occur at slow rates. Here, we report that biostimulation and bioaugmentation enhanced dechlorination of low concentration (2.1 mg PCBs/kg dry weight) historical PCBs in microcosms prepared with Anacostia River, Washington, DC, sediment. Treatments included electron donors butyrate, lactate, propionate and acetate (1 mM each); alternate halogenated electron acceptors (haloprimers) tetrachlorobenzene (TeCB, 25 μM), pentachloronitrobenzene (PCNB, 25 μM), or 2,3,4,5,6-PCB (PCB116, 2.0 μM); and/or bioaugmentation with a culture containing Dehalococcoides ethenogenes strain 195 (3 × 10⁶ cells/mL). Dechlorination rates were enhanced in microcosms receiving bioaugmentation, PCNB and PCNB plus bioaugmentation, compared to other treatments. Microcosm subcultures generated after 415 days and spiked with PCB116 showed sustained capacity for dechlorination of PCB116 in PCNB, PCNB plus bioaugmentation, and TeCB treatments, relative to other treatments. Analysis of Chloroflexi 16S rRNA genes showed that TeCB and PCNB increased native Dehalococcoides spp. from the Pinellas subgroup; however this increase was correlated to enhanced dechlorination of low concentration weathered PCBs only in PCNB-amended microcosms. D. ethenogenes strain 195 was detected only in bioaugmented microcosms and decreased over 281 days. Bioaugmentation with D. ethenogenes strain 195 increased PCB dechlorination rates initially, but enhanced capacity for dechlorination of a model congener, PCB116, after 415 days occurred only in microcosms with enhanced native Dehalococcoides spp.     

Organohalogenated contaminants in eggs of rockhopper penguins (Eudyptes chrysocome) and imperial shags (Phalacrocorax atriceps) from the Falkland Islands

In this study, we evaluated the use of seabird eggs of two common bird species from the Falkland Islands as bioindicators of contamination with organohalogenated contaminants (OHCs). We compared contamination levels and profiles of different OHCs between eggs of the rockhopper penguin (Eudyptes chrysocome) and the imperial shag (Phalacrocorax atriceps). In addition, laying order effects on OHC concentrations and profiles were also investigated in both species. For polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs) as well as polybrominated diphenyl ethers (PBDEs), concentrations were significantly lower in eggs of rockhopper penguins (27.6 ± 0.70 ng/g lw, 56.5 ± 1.33 ng/g lw and 0.98 ± 0.04 ng/g lw, respectively) compared to the imperial shags (140 ± 5.54 ng/g lw, 316 ± 11.53 ng/g lw, 1.92 ± 0.15 ng/g lw, respectively). On the other hand, 2′MeO-BDE 68 and 6MeO-BDE 47, two brominated compounds of reported natural origin, were significantly higher in the penguin eggs (0.55 ± 0.05 ng/g lw and 7.01 ± 0.64 ng/g lw, respectively) compared to the shag eggs (0.17 ± 0.03 ng/g lw and 0.50 ± 0.06 ng/g lw, respectively). In addition, PCB, OCP and PBDE contamination profiles differed markedly between the two species. Various factors, such as diet, feeding behaviour, migratory behaviour and species-specific metabolism, may be responsible for the observed results. For both rockhopper penguins and imperial shags, PCB, OCP and PBDE concentrations and profiles did not significantly change in relation to the laying order. This suggests that, for both species, any egg of a clutch is useful as a biomonitoring tool for OHCs. Although our results showed that OHCs have also reached the Falkland Islands, concentrations were relatively low compared to other studies. However, future monitoring may be warranted to assess temporal trends of different OHCs.     

Distribution of polychlorinated biphenyls, organochlorine pesticides and polybrominated diphenyl ethers in human umbilical cord serum, maternal serum and milk from Wielkopolska region, Poland

The levels of organochlorinated pesticides (OCPs): p,p'-DDT and its metabolites, hexachlorobenzene (HCB), hexachlorocyclohexane isomers (HCHs), chlordanes and their metabolites, and 18 polychlorinated biphenyl (PCB) congeners were measured in maternal serum, umbilical cord serum and human milk collected from 22 mothers living in the Wielkopolska region, Poland. Additionally, 11 polybrominated diphenyl ether (PBDE) congeners were measured in the human milk samples. p,p'-DDT and its major metabolite, p,p'-DDE, together with HCB, were found in all milk and serum samples. Median concentrations of p,p'-DDE in maternal serum, umbilical cord serum and milk were 343, 329 and 634ng/g lipid weight (lw). PCB congeners 138, 153 and 180 were the major congeners measured in all serum samples, while CB 170 was detected in 74% and 100% of umbilical cord and maternal serum, respectively. Except for CBs 74, 101 and 105, which had a detection frequency of 77%, 23% and 82%, respectively, all investigated PCB congeners were measured in all human milk samples. The median concentrations of sum PCBs in maternal serum, umbilical cord serum and milk were 79, 60 and 133 ng/g lw, respectively. A good correlation (Spearman R(S)>0.75, p<0.001) was found for major PCBs, p,p'-DDT and p,p'-DDE, between maternal and umbilical cord serum, while the correlation was weaker between milk and serum. The median of sum PBDEs in human milk was 2.0 ng/g lw (range 0.8 to 8.4), with BDE 47 being always the most abundant PBDE congener and, together with BDE 153, being present in all samples. In general, results found in the investigated group are at the low end of the concentration range measured in Europe.     

PBBs, PBDEs, and PCBs levels in hair of residents around e-waste disassembly sites in Zhejiang Province, China, and their potential sources

This study was conducted to explore the exposure potential of Chinese residents to PBBs, PBDEs, and PCBs in e-waste disassembly sites in Zhejiang province. The contents of 23 PBB congeners, 12 PBDE congeners, and 27 PCB congeners in hair and in their potential sources, including soil and e-waste, were measured via GC-MS. The levels of PHAHs in the three subfamilies (i.e., the PBBs, PBDEs, and PCBs) were all considerably higher (P<0.05) in hair samples collected from the disassembly sites than from the control site. The highest levels of PBBs (57.77 ng g(-1) dw), PBDEs (29.64 ng g(-1) dw), and PCBs (181.99 ng g(-1) dw) in hair were all found in those from the disassembly site Xinqiu, which are respectively 2, 2, and 10 times more than those observed in hair from the control site Yandang. Among the three subfamilies of PHAHs, PCBs were the most predominant pollutants detected. PBBs, which have very limited information available in China, can be detected at a comparable level with PBDEs in these samples in the study. Therefore, these observations suggested that more attention should be given over the potential for environmental or occupational exposure to PHAHs present in e-waste. By and large, the PHAH levels measured in the hair samples were consistent with those detected in the soil. Hair analysis could thus be a valid screening tool for assessing human PHAHs exposure in and around e-waste disassembly sites.     

Polybrominated diphenyl ether (PBDE) flame retardants

Polybrominated diphenyl ether, PBDE, flame retardants are now a world-wide pollution problem reaching even remote areas. They have been found to bioaccumulate and there are concerns over the health effects of exposure to PBDEs, they also have potential endocrine disrupting properties. They are lipophilic compounds so are easily removed from the aqueous environment and are predicted to sorb onto sediments and particulate matter or to fatty tissue, aiding their distribution throughout the environment. PBDEs are structurally similar to PCBs and DDT and, therefore, their chemical properties, persistence and distribution in the environment follow similar patterns. Concentrations of PBDEs found in environmental samples are now higher than those of PCBs. Evidence to date demonstrates that PBDEs are a growing problem in the environment and concern over their fate and effects is warranted. The manufacture of reactive and additive flame retardants is briefly discussed and their fate and behaviour in the environment is assessed. PBDE toxicology is reviewed and methods of analysis are evaluated.     

Spatial and temporal changes of chlorinated pesticides, PCBs, dioxins (PCDDs/PCDFs) and brominated flame retardants in human breast milk from Northern Russia

This study presents for the first time temporal changes of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in Russian human breast milk samples. Concentrations of OCPs and PCBs in samples from three locations in the North West of Russia in 2000-2002 (n=42), were compared to corresponding levels measured in 1993-1996 (n=58). In addition brominated flame retardants (BFRs), consisting of polybrominated diphenylethers (PBDEs) (including BDE-209) and hexabromocyclododecane (HBCD) were analysed in samples from 2000-2002 (n=37). The present levels of SigmaDDTs and SigmaHCHs were 5 and 10 times higher than corresponding levels in the neighbouring country Norway. Median concentrations of SigmaHCHs (196 microg/kg lw), SigmaCHBs (19.7 microg/kg lw) and SigmaPCBs(16) (316 microg/kg lw) were highest in Murmansk. The percentage of p,p'-DDT to SigmaDDTs and ratio DDE/DDT suggest possible ongoing use of DDT in Russia. Levels of PBDE were low and dominated by the congeners BDE-47 and BDE-153. The deca brominated BDE-209 was detected in all analysed samples (median concentration 0.19 microg/kg lipid). Levels of SigmaOCPs and SigmaPCBs decreased 56 and 30% in Murmansk and 36 and 43% in Arkhangelsk during the study period. The decline of SigmaOCPs was significant at both locations (p<0.05-p<0.0001). For SigmaPCBs, the decreasing trend was only significant in Arkhangelsk (p<0.0001). In addition, a decline of Sigmatotal TEQs (SigmaTEQs of PCDDs/PCDFs, non-ortho- and mono-ortho PCBs) was observed in Murmansk and Arkhangelsk during the study period. The exposure of infants by PCDDs/PCDFs and dioxin-like PCBs is still exceeding the daily tolerable intake (TDI) in North West Russia. However, the concentrations of PCDDs/PCDFs and dioxin-like PCBs seem to decline very rapidly.     

Polychlorinated biphenyls (PCBs) in sediments of the southern Baltic Sea — trends and fate

Polychlorinated biphenyls (PCBs) have been determined in recent [0–1(2), 1(2)–5 and 5–10 cm deep layers] sediments from different sites of the southern Baltic Sea, including the Szczecin Lagoon, collected from May 1996 to October 1999, i.e. before and after the great flood in Poland of July/August 1997. The PCB distribution has been correlated with location and hydrological conditions as well as with organic carbon, algal pigments and their derivatives in the sediments. The sum of PCB (seven congeners) was equal to 1–149 ng/g dry wt., on average this was rather low (up to 40 ng/g). There was a decreasing trend in PCBs concentrations in the bottom sediments of the southern Baltic in 1996 but considerable amounts were still accumulated there. The flood of 1997 caused a distinct increase of PCB concentration level in the sediments, which again showed a decreasing trend in the next few years. This illustrates that at present the main source of PCBs for the southern Baltic are not a direct consequence of human activity, but from floods and heavy rains washing these compounds from land to the sea. Algae and algal detritus play an important role in the transport and distribution of PCBs in the southern Baltic. High correlation of PCBs with chlorophyll a derivatives — products of zooplankton grazing — indicates that PCBs are ingested by zooplankton with phytoplankton and then exuded with fecal pellets. PCBs bound to algal detritus or to fecal pellets in the water column are transferred to sediments, there they may be trapped either in a bonded and unchanged form or resuspended, remobilized and/or dechlorinated, depending on their properties and environmental conditions.     

Sedimentation of polychlorinated biphenyls (PCBs) in limnic and marine environments

The sedimentation rates of PCBs in two southern Swedish lakes and a coastal bay in the southern Baltic were determined using sediment traps. The rates were similar at the three locations and ranged from 1.2 to 10.9 μg PCBs m⁻² month⁻¹ during summer. The source for PCBs in sedimenting material is probably the atmosphere. PCB concentrations in sedimenting material were higher than those in surface sediment. This may be due to recirculation of sediment-bound PCBs.The reproducibility of collecting by sediment traps was examined by deploying duplicate traps simultaneously. There were no significant differences in PCB concentration of sedimenting material between traps placed in duplicate. Concentrations of PCBs in the different collecting vessel was similar within one trap.