Polychlorinated biphenyls (PCBs) and polybrominated biphenyl ethers (PBDEs) in environmental samples from Ny-Ålesund and London Island, Svalbard, the Arctic.

Polychlorinated biphenyls (PCBs) and polybrominated biphenyl ethers (PBDEs) were determined in environmental samples collected from Ny-Ålesund and London Island, Svalbard, the Arctic. Total PCB concentrations (∑25PCBs) varied from 0.57 to 2.52 ng g(-1) dry weight (dw) in soil, 0.30 to 1.16 ng g(-1) dw in plants and 0.56 to 0.98 ng g(-1) dw in reindeer dung. The non-Aroclor congener of CB-11 was predominant in most samples compared to other congeners, accounting for 16.0±9.8% to the ∑25PCBs. The ∑13PBDEs concentrations were 1.7-416, 36.7-495 and 28.1-104 pg g(-1) dw in soil, plants and reindeer dung, respectively. The signature of enantioselective biotransformation was observed in all samples for chiral CB-95, whereas in parts of samples for other chiral PCBs. Bioaccumulation factors (BAFs) in six plant species varied within individual contaminant congeners and plant species, with BAFs less than 1 for ∑PCBs and higher than 1 for ∑PBDEs. BAF values decreased with increasing soil concentrations, suggesting that high background levels in soil restricted the accumulation of these contaminants by plants.

Polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans and polybrominated diphenyl ethers in sediments and fish species from the Murchison Bay of Lake Victoria, Uganda.

Polychlorinated dibenzo-p-dioxins/furans (PCDD/Fs) and polybrominated diphenyl ethers (PBDEs) were analyzed in sediments and fish from the Murchison Bay of Lake Victoria by high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS). Average concentrations of total (Σ) PCDD/Fs and ΣPBDEs in sediments ranged from 68.8 to 479 pg g(-1) dry weight (dw) and 60.8 to 179 pg g(-1) dw, respectively. Contamination levels of sedimentary PCDD/Fs and PBDEs were low to moderate compared to other urbanized regions worldwide. The concentrations in different fish species (Nile perch; Lates niloticus and Nile tilapia; Oreochromis niloticus) were 5.32 to 49.0 pg g(-1) wet weight (ww) for PCDD/Fs and 59.3 to 495 pg g(-1) ww for PBDEs. Higher concentrations of the pollutants were found in L. niloticus than O. niloticus, which could be attributed to species differences in feeding habits and lifestyles. World Health Organization-toxic equivalents (WHO2005-TEQs) for PCDD/Fs ranged from 0.08 to 0.33 pgTEQg(-1) dw and 0.001-0.14 pg TEQg(-1) ww in sediments and fish, respectively. The TEQ values were low compared to the data for fresh water fish reported in literature and within a permissible level of 3.5 pg g(-1) ww recommended by the European Commission. Based on the Commission set value and minimum risk level criteria formulated by the Agency for Toxic Substances and Disease Registry, the fish from the Murchison Bay was fit for human consumption.

Dioxins contamination in the feed additive (feed grade cupric sulfate) tied to chlorine industry.

The sources of polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) found in animal feed additive (feed grade cupric sulfate, CuSO4) were investigated and traced back to the formation of chlorinated organic compounds in the chlor-alkali industry. PCDD/Fs could be transported through the supply chain: hydrochloric acid (HCl) by-produced during formation of chlorinated organic compounds in chlor-alkali industry → spent acid etching solution (acid-SES) generated in printed circuit board production → industrial cupric salt → CuSO4 in animal feed, and finally enter the food chain. The concentration ranges in HCl and acid-SES were similar, of which the level in acid-SES was also consistent with that in various cupric salt products including CuSO4 based on Cu element content. PCDD/Fs also showed very similar congener profiles in all the sample types. This indicates a probable direct transport pathway of PCDD/Fs into the food chain, which may eventually be exposed to humans through consumption. To date this is the first study in China that systematically reports on the PCDD/Fs transport from industrial pollution sources to industrial processes and finally enters the human food chain.

Polychlorinated biphenyls and hexachlorocyclohexanes in sediments and fish species from the Napoleon Gulf of Lake Victoria, Uganda.

Polychlorinated biphenyls (PCBs) and hexachlorocyclohexanes (HCHs) were analyzed in surface sediments (<30 cm depth) and two fish species: Nile perch (Lates niloticus) and Nile tilapia (Oreochromis niloticus). The samples were collected from the Napoleon Gulf on the northern shore of Lake Victoria. The analysis was done using a gas chromatograph (GC) coupled to a high resolution mass spectrometer for PCBs and a GC equipped with an electron capture detector for HCHs. Total (Σ) PCBs in the muscles of fish varied widely with mean values ranging from 41 to 670 pg g(-1) lipid weight (lw). The PCB levels in L. niloticus were significantly greater than those in O. niloticus. The large variability observed in the data was attributed to differences in feeding habits and trophic levels. While O. niloticus is a filter-eating fish species feeding mainly on phytoplankton and zooplankton, L. niloticus have predatory feeding behaviors and prefer a diet of live fish and, therefore, are more prone to bio-accumulate contaminants. The mean PCB concentrations in the sediments varied from 362 to 848 pg g(-1) dry weight. Variations in PCB levels were observed from one study site to another, this was attributed to the nature and particle size of the sediments. HCH isomers were detected in fish at mean concentrations of up to 45,900 pg g(-1) lw. The PCB and HCH concentrations were lower than those from previous studies elsewhere in literature and were below the maximum residue limits set by the European Commission and FAO/WHO Codex Alimentarius Commission, implying that the fish was fit for human consumption.

Polychlorinated biphenyls in sediments and fish species from the Murchison Bay of Lake Victoria, Uganda.

Polychlorinated biphenyls (PCBs) were determined in sediments and two fish species collected from the Murchison Bay in Lake Victoria, using high resolution gas chromatography coupled to a high resolution mass spectrometer. Total PCB concentrations (Σ18PCBs) varied widely with mean values ranging from 777 to 4325pg g(-1) dry weight (dw) for sediments and 80 to 779pg g(-1) wet weight (ww) for fish. The PCB levels in the sediments were significantly higher at the station closest to Nakivubo channel, presumably due to effluents discharged by the channel, which may contain domestically produced commercial PCB mixtures. For fish, the concentrations in Nile perch (Lates niloticus) were significantly greater than those in Nile tilapia (Oreochromis niloticus) at all study stations, possibly due to dietary differences among species. World Health Organization-toxic equivalents (WHO2005-TEQs) for the dioxin-like PCBs were 0.04-0.64pg g(-1) dw and 0.01-0.39pg g(-1) ww for sediments and fish, respectively. The non-ortho PCBs exhibited the highest contribution to the Σ12TEQs (>75%) compared to the mono-ortho PCBs in both fish species. The TEQs in the present study were lower than many reported worldwide in literature for fish and were within the permissible level recommended by the European Commission, implying that the fish did not pose health hazards related to PCBs to the consumers.

[Identification of two interference peaks during dioxin analysis for biological samples].

Two interference peaks which generally appeared in company with 13C labeled 2,3,7,8-tetrachlorodibenzofuran (13C12-2,3,7,8-TCDF) in the same ion channel during dioxin analysis for biological samples were identified using high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS) and high resolution gas chromatography/low resolution mass spectrometry (HRGC/LRMS). It was firstly inferred that the interference peaks should be the two isomers of dichlorodiphenyldichloroethylene (DDE), which was a breakdown product of dichlorodiphenyltrichloroethane (DDT), one of the typical organic chlorine pesticides (OCPs). Thereafter, the standard solution of DDE including o,p'-DDE and p,p'-DDE was analyzed for confirmation. By evaluation of the peak separation in HRGC/HRMS, comparison of the GC retention times and ion abundance ratios of the two interference peaks in real samples with the two DDE isomers in standard solution, the interference peaks were finally confirmed as o,p'-DDE and p,p'-DDE in sequence on a DB-5MS column. This study provided valuable information for accurate identification of dioxin compounds during the biological sample analysis.

Temporal trends of PCBs, PCDD/Fs and PBDEs in soils from an E-waste dismantling area in East China.

The temporal trends of polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polybrominated diphenyl ethers (PBDEs) were investigated in soils from an E-waste dismantling area in East China between 2005 and 2011. Isotope dilution high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS) was employed for the sample analysis. PCB levels declined as expected, while PCDD/Fs generally remained at a constant level during the sampling period, and PBDE concentrations tended to be slightly lower after 2007 although the decline was not statistically significant. The congener profiles indicated that lowly-halogenated congeners of these persistent organic pollutants (POPs) accounted for the decreasing levels and relative proportions of the POPs, suggesting that they have been gradually eliminated from the field soil over the years. However, the concentration levels of some heavy congeners (e.g., CB-209, OCDD and OCDF) showed different trends from those of the lighter ones. The general tendencies of the three types of POPs in soils were consistent with those reported in other studies in this area. The results implied that the enhanced regulations and centralized dismantling action introduced in 2005 might exert a limited influence on these three types of POPs in soils during the sampling period.

Levels and profiles of Dechlorane Plus in a major E-waste dismantling area in China.

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 1,990 ng g(-1) dw in soil samples and 3.43 to 89.2 ng g(-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.

Bioaccumulation of PCDD/Fs, PCBs and PBDEs by earthworms in field soils of an E-waste dismantling area in China.

A total of 60 paired samples of earthworm, corresponding soil and wormcast were collected to investigate the bioaccumulation tendency of polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in earthworms from a typical E-waste dismantling area in east China. Significant correlations were observed for the total concentrations among different matrix types except for PCDD/Fs in soil and earthworm. The bioaccumulation tendency showed some differences among the contaminants. Calculated biota-soil accumulation factors (BSAFs) indicated that PCBs and PBDEs had higher bioaccumulation potential compared to PCDD/Fs, which was somewhat different from laboratory studies. The plot of mean BSAFs versus log Kow values for PCBs and PBDEs was well fitted by a second-order polynomial with the maximum BSAF at approximately log Kow of 6.5. While for PCDD/Fs, only a slightly decreasing trend was observed with increasing log Kow. Composition analysis indicated that tetra-, penta- and hexa-halogenated homologs had higher bioaccumulation levels, indicating that medium-halogenated congeners with log Kow around 6.5 are more easily accumulated by earthworms. Furthermore, the ratios of BDE-47/-99 and BDE-99/-100 showed some discrepancies with the technical products and other biotic species, suggesting different bioaccumulation potential of PBDEs in earthworm.