Fate, residues and dietary risk assessment of the fungicides epoxiconazole and pyraclostrobin in wheat in twelve different regions, China.

The fungicides epoxiconazole and pyraclostrobin have been widely used to control wheat fusarium head blight. This study was designed to investigate the dissipation behaviors in different climate regions and provide data for the modification of maximum residue limits of the two fungicides. Wheat samples were collected from field sites in twelve different regions, China and analyzed with an HPLC-MS/MS method for simultaneous detection of epoxiconazole and pyraclostrobin in wheat. The average recoveries of epoxiconazole and pyraclostrobin in wheat matrix were 87-112% and 85-102%, respectively, with the relative standard deviations ≤8.1%. The limits of quantification of epoxiconazole and pyraclostrobin in grain and straw were both 0.01 mg/kg. The dissipations of epoxiconazole and pyraclostrobin followed first-order kinetics, with the half-lives of 10.3 days and 7.6 days, respectively. The terminal residues of epoxiconazole and pyraclostrobin in grain were below 0.034 and 0.028 mg/kg, separately, both lower than the maximum residue limits recommended by China. Based on Chinese dietary pattern and terminal residue distributions, the risk quotients of epoxiconazole and pyraclostrobin were 13.9% and 65.9%, respectively, revealing the evaluated wheat exhibited an acceptably low dietary risk to consumers.

Antibiotics and Food Safety in Aquaculture.

Antibiotics are widely used in aquaculture. Intensive farming drives indiscriminate use of antibiotics, which results in residues of antibiotics in cultured aquatic products and bacterial resistance. This perspective attempts to present a brief update on usage, regulations, residues, and potential human health risk of antibiotics used in aquaculture. Through the comprehensive literature review, we provide a view that the safety of aquatic products still requires further attention and more rigorous risk assessment. Finally, we make a few suggestions for future research directions: reduce the use of antibiotics to bring down the speed of resistance development and monitor resistant pathogens and genes, strictly manage the environmental sanitation of aquaculture and pay attention to the quality of water bodies introduced into aquaculture, seek international cooperation to establish an information bank of antibiotic residues and antibiotic-resistant genes, and set up a quantitative model to assess the risk of antibiotic resistance associated with the antibiotic residues.

Bioaccumulation and human health risk assessment of DDT and its metabolites (DDTs) in yellowfin tuna (Thunnus albacares) and their prey from the South China Sea.

DDTs were detected in yellowfin tuna (Thunnus albacares, 92.1-221.8 ng‧g-1 lipid weight) and their prey (54.9-93.5 ng‧g-1 lipid weight) from the South China Sea (SCS). DDT levels reported in this study were lower than those of the previous studies indicated the recent mitigation of DDT contamination in the SCS. Higher DDT levels were observed in fat abdominal muscle than lean dorsal muscle in adult yellowfin tuna. Meanwhile, DDT levels in adult yellowfin tuna were higher than the young ones. The composition profiles of DDT and its metabolites suggested DDTs in fish in the SCS were mainly derived from the historical use of technical DDTs. DDTs were biomagnified through food chains with the trophic magnification factor of 2.5. Risk assessment results indicated that dietary exposure to DDTs through lifetime fish consumption from the SCS would pose little cancer and noncarcinogenic risk to coastal residents.

Bioaccumulation of short-chain chlorinated paraffins in chicken (Gallus domesticus): Comparison to fish.

Short chain chlorinated paraffins (SCCPs) are a complex group of chlorinated organic pollutants that have raised an increasing public attention. However, limited information is currently available on the bioaccumulation of SCCPs in terrestrial birds which are abundant and widely distributed around the world. In the present study, chicken (Gallus domesticus) was used as a model organism to provide significant implications for other avian species. We investigated the transfer of SCCPs from dietary sources (feed and topsoil) to chicken and their tissue distribution behavior. SCCPs were detected in chicken feed (54-170 ng/g, dry weight), topsoil (170-860 ng/g, dry weight), and adult chicken tissues (460-13000 ng/g, lipid weight). Adult chicken tended to accumulate SCCP congeners with lower n-octanol-water partition coefficients (KOW) and octanol-air partition coefficients (KOA). The accumulation ratio values for SCCPs of the chicken were more influenced by KOA than by KOW, which was contrary to those for aquatic fish. Levels and homologue profiles of SCCPs varied among chicken tissues. SCCP levels in the livers were significantly lower than those in the other tissues (p < 0.05). The accumulation potential for SCCP congeners with higher KOW increased in the order of muscle < liver < fat.

Geographical distribution and risk assessment of dichlorodiphenyltrichloroethane and its metabolites in Perna viridis mussels from the northern coast of the South China Sea.

Mussels (Perna viridis) were collected from the northern coast of the South China Sea (NSCS) to investigate the geographical distribution and potential risk of dichlorodiphenyltrichloroethane and its metabolites (DDTs). DDTs had concentrations that ranged from 248 ng/g to 4650 ng/g lipid weight (lw), with an average of 807 ± 932 ng/ng lw. A comparison of the levels of DDTs in mussels indicated that the NSCS is still one of the most polluted areas in the world, although a decreasing trend was observed. DDT metabolites were predominant in all samples, suggesting that historical residue was the main source of DDT pollution. However, there were new inputs of DDTs which likely associated with antifouling paints. The human health risk assessment revealed that the current concentrations of DDTs in mussels might pose little health risk for the consumers.

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.

Occurrence and congener profiles of polybrominated diphenyl ethers in green mussels (Perna viridis) collected from northern South China Sea and the associated potential health risk.

Polybrominated diphenyl ether (PBDE) contamination has become a major concern over the effects on human health. In the present study, we collected widely consumed green mussels (Perna viridis) samples from the northern South China Sea (NSCS) to investigate the occurrence, spatial distribution, congener profiles as well as potential risk of 18 PBDEs. All the target PBDEs were detected in green mussel samples, indicating their ubiquitous distribution. The concentrations of the total 18 PBDES (ΣPBDEs) in all samples varied from 6.96 to 55.6 ng/g lipid weight (lw), with BDE-47 and BDE-209 being the predominant PBDE congeners. Overall, the ΣPBDEs pollution in green mussels from NSCS was at a moderate to high level in comparison with the PBDEs pollution worldwide. The dietary exposure of the local population in South China to PBDEs via consuming green mussels was estimated to be 0.30-0.80 ng/kg body weight (bw)/day. Evaluation of the exposure risk for BDE-47, 99, 153 and 209 indicated that health risks due to green mussel consumption are substantially lower than the U.S. EPA minimum concern level.

Contamination Evaluation and Source Identification of Heavy Metals in the Sediments from the Lishui River Watershed, Southern China.

Seven heavy metals (Cr, Mn, Co, Ni, Cu, Zn, Pb) were measured in surface sediments from the Lishui River watershed, an area with increased soil erosion in China. The mean concentrations of heavy metals were 61.20 mg/kg (Cr), 757.15 mg/kg (Mn), 9.39 mg/kg (Co), 25.31 mg/kg (Ni), 22.84 mg/kg (Cu), 91.66 mg/kg (Zn), and 40.19 mg/kg (Pb), respectively. The spatial distribution of heavy metals was site-specific, exhibiting a remarkably high level in the sampling stations with intense agricultural activities (Lixian) and industrial activities (Jinshi). Contamination indexes including contamination factor, pollution load index, nemerow multi-factor index, potential ecological risk index, and human health risk were used to assess the pollution degree of the river sediments. The results indicated the pollution degree of heavy metals decreased in the order of Mn>Pb>Zn>Cr>Cu>Ni>Co. Heavy metals resulted in non-pollution to moderate pollution, with low ecological risk and an acceptable carcinogenic risk caused by Cr and Ni for children and adults. Person's correlation analysis and principal component analysis, coupled with cluster analysis, revealed that the sediments from the Lishui River were mainly influenced by two sources. Cr, Co, Ni, and Cu were mainly derived from natural sources, while Mn, Zn, and Pb originated from agricultural and industrial activities, mining, and vehicular traffic.

Size-dependent concentrations and bioaccessibility of organophosphate esters (OPEs) in indoor dust: A comparative study from a megacity and an e-waste recycling site.

Indoor dust ingestion is an important pathway in human exposure to environmental pollutants, and the bioaccessibility of pollutants can largely influence human exposure risk assessment. In the present study, the concentrations and compositions of organophosphate esters (OPEs) were investigated for different sizes (50 µm to 2 mm) of indoor dust collected from a megacity, Guangzhou, and an e-waste recycling site. The concentrations of total OPEs were 5360 to 6830 ng/g and 560 to 20,500 ng/g across all sizes of dust from Guangzhou and the e-waste site, respectively. The levels and compositions of OPEs were consistent in different fractions of dust from Guangzhou. The highest concentrations of OPEs were found in the finest fraction of dust from the e-waste site. OPEs in Guangzhou dust showed decreasing bioaccessibility when the log KOW of FRs increased from 4 to 11. The bioaccessibility of most OPEs in dust from the e-waste site was much lower than those in Guangzhou dust, indicating low bioaccessibility in the components of dust, such as e-waste debris, from the e-waste site. The human exposure risks of OPEs in dust from Guangzhou were generally higher than those in dust from the e-waste site. Chitosan and montmorillonite could significantly decrease the bioaccessibility of all OPEs, except for tri-ethyl phosphate (TEP) and tris­(2­butoxyethyl) phosphate (TBOEP) in dust (p < 0.05), indicating chitosan and montmorillonite as promising food additives to enhance the elimination of OPEs.

Polycyclic aromatic hydrocarbons in sediments and marine organisms: Implications of anthropogenic effects on the coastal environment.

Intensive human activities aggravate environmental pollution, particularly in the coastal environment. Sixteen priority polycyclic aromatic hydrocarbons (PAHs) were determined in the sediments and marine species from Zhanjiang Harbor, a large harbor in China. The total PAH concentrations ranged from 151 to 453 ng/g dry weight (dw) in sediments and from 86.7 to 256 ng/g wet weight (ww) in organism tissues. High levels of PAHs occurred in the sample sites next to the estuary. A decrease in PAH levels was observed in comparison to the previous survey prior to 2012. Fish exhibited lower lipid weight normalized PAH concentrations than the other species, which may be related to their efficient metabolic transformation. Three ring PAHs dominated both in marine sediments and species, but low molecular weight PAHs exhibited higher proportions in biota than in sediments (p < 0.05). Petrogenic and pyrolytic sources both contributed to the occurrence of PAHs, and the latter became increasingly important in the study area. The ecological risk from PAHs in the sediments was relatively low (9% incidence of adverse biological effect) according to the effects-based sediment quality guideline values. Exposure to PAHs via consuming seafoods might pose a health risk to local residents. Overall, these results revealed anthropogenic activities in the coastal area have an impact on the local ecosystem.

The distribution and accumulation of phosphate flame retardants (PFRs) in water environment.

Phosphate flame retardants (PFRs) were measured in surface water (n=11), suspended particle matter (SPM, n=11), sediment (n=11), and fish samples (n=26) from the Pearl River Delta located in South China. Triethyl phosphate (TEP), tri(2-chloroethyl) phosphate (TCEP), tris(chloroisopropyl) phosphate (TCIPP), tri-n-butyl phosphate (TNBP), triphenyl phosphate (TPHP), and tricresyl phosphate (TMPP) were detected in more than half of surface water, SPM, and sediment samples. The median ΣPFR levels were 837ng/L, 54.6ng/g dry weight (dw), and 37.1ng/g dw in surface water, SPM, and sediment samples, respectively. No significant correlations were found between the concentrations of most PFRs and organic carbon contents in SPM and sediment (p>0.05). In surface water samples, tris(2-butoxyethyl) phosphate (TBOEP, 27% of ΣPFRs) and TEP (23% of ΣPFRs) were the predominant chemicals, while TNBP (38% of ΣPFRs) and TCEP (32% of ΣPFRs) dominated in ΣPFRs in SPM samples, and TCEP (48% of ΣPFRs) and TCIPP (25% of ΣPFRs) dominated in ΣPFRs in sediment samples. The proportions of phenyl-PFRs and chlorinated-PFRs in ΣPFRs increased from surface water to SPM and sediment. The distribution ratios of PFRs between water and organic carbon in SPM (or observed KOC) were generally 2-3 orders of magnitude higher than the predicted KOC. TNBP (nd-2.42ng/g wet weight (ww)), TCEP (nd-4.96ng/g ww), and TCIPP (nd-2.42ng/g ww) were detected in 27%, 35%, and 23% of all fish samples, respectively. The log bioaccumulation factors (BAFs) ranged 2.56-2.78, 2.15-3.11, and 2.61-3.10 for TNBP, TCEP, and TCIPP, respectively. The biota-sediment accumulation factors (BSAFs) of TNBP, TCEP, and TCIPP were generally lower than 1 except for the BSAF of TCIPP in common carp. The results indicate the species-specific bioaccumulation of PFRs in fish species.

Hexabromocyclododecanes (HBCDs) in fish: Evidence of recent HBCD input into the coastal environment.

Hexabromocyclododecanes (HBCDs) are flame retardants and emerging persistent organic pollutants. In the present study, α-, ß-, and γ-HBCDs were measured in several fish species from rivers and an electronic waste (e-waste) recycling site in Pearl River Delta, South China. The concentrations of HBCDs were 12.8 to 640, 5.90 to 115, and 34.3 to 518ng/g lipid weight (lw) in mud carp (Cirrhinus molitorella), tilapia (Tilapia nilotica), and plecostomus (Hypostomus plecostomus), respectively. Plecostomus showed the highest HBCD concentrations among three fish species. The contributions of α-HBCD to total HBCDs were 78% to 97%, 93% to 99%, and 87% to 98% in carp, tilapia, and plecostomus, respectively. Fish samples from a harbor and the e-waste site exhibited the highest HBCD concentrations among all samples. The HBCD concentrations were not significantly correlated with the gross domestic product or population data. e-Waste recycling activities, harbor construction, and shipment might be recent HBCD sources.

Stereoselective bioaccumulation of syn- and anti-Dechlorane plus isomers in different tissues of common carp (Cyprinus carpio).

Common carps (Cyprinus carpio) were exposed to syn- and anti-Dechlorane Plus (DP) isomers to investigate absorption, tissue distribution, and stereoselective bioaccumulation of DP isomers. The absorption efficiencies of anti-DP in the gastrointestinal system were higher than those of syn-DP. A linear accumulation was found for both isomers in all fish tissues except for serum; and the liver and gill exhibited the highest and lowest DP assimilation efficiency, respectively. The elimination of DP isomers in all tissues followed first-order kinetics, with the fastest depuration rate occurring in the liver and serum. The biomagnification factors (BMFs) of both isomers were less than one in all tissues, except for serum. Anti-DP was preferably accumulated in the liver, gill, and serum, whereas syn-DP was selectively accumulated in the carcass and gastrointestinal tract. As a whole, fish did not show selective accumulation of the syn- or anti-DP isomer in the uptake stage, whereas a selective accumulation of syn-DP in fish was observed during the depuration period, which could be due to a selective excretion of anti-DP. Metabolism cannot be ruled out as a possible reason considering the high fanti values and the high elimination rate of DPs in the liver.

Legacy and emerging organohalogenated contaminants in wild edible aquatic organisms: Implications for bioaccumulation and human exposure.

Highly industrialized and urbanized watersheds may receive various contaminants from anthropogenic activities. In this study, legacy and emerging organohalogenated contaminants (OHCs) were measured in edible wild aquatic organisms sampled from the Pearl River and Dongjiang River in a representative industrial and urban region in China. High concentrations of target contaminants were observed. The Pearl River exhibited higher concentrations of OHCs than the Dongjiang River due to high industrialization and urbanization. Agrochemical inputs remained an important source of OHCs in industrialized and urbanized watershed in China, but vigilance is needed for recent inputs of polychlorinated biphenyls (PCBs) originated from e-waste recycling activities. Bioaccumulation of dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexanes (HCHs), PCBs, polybrominated diphenyl ethers (PBDEs), and Dechlorane Plus (DP) was biological species- and compound-specific, which can be largely attributed to metabolic capability for xenobiotics. No health risk was related to the daily intake of DDTs, HCHs, and PBDEs via consumption of wild edible species investigated for local residents. However, the current exposure to PCBs through consuming fish is of potential health concern.

Flame retardants on the surface of phones and personal computers.

Mobile phones and personal computers (PCs) are essential products that are frequently contacted in daily life. Thus, phones and computers containing flame retardants (FRs) may play vital roles in human exposure to FRs. We measured several FRs, including polybrominated diphenyl ethers (PBDEs), 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), decabromodiphenyl ethane (DBDPE), tetrabromobisphenol (TBBPA), and phosphate flame retardants (PFRs), on the surfaces of phones and PCs (laptop keyboards and mice). Triphenyl phosphate (TPHP, 228pg/cm2) and tris(chloroisopropyl) phosphate (TCIPP, 43pg/cm2) were the most abundant chemicals on the surfaces of phones, while TPHP (65pg/cm2), TCIPP (48pg/cm2), and DBDPE (22pg/cm2) were dominant on the surfaces of PCs. The usage time and time after the production of the electronics were not significantly correlated with the FR concentrations, except for that of BDE 209. The concentrations of FRs differed on the surfaces of different brands of electronics. Dermal contact with the surface of electronics may contribute to human exposure to FRs, which should be of concern.

Brominated and phosphate flame retardants (FRs) in indoor dust from different microenvironments: Implications for human exposure via dust ingestion and dermal contact.

Indoor dust has been widely used to monitor flame retardants (FRs) in indoor environment, but most studies only focused on floor dust. In the present study, FRs were examined in indoor dust from different locations. Dust from air conditioner (AC) filters, beddings, floor, and windows in bedrooms, and dust from AC filters, printer table surface, computer table surface, floor, and windows in offices were collected, respectively. Polybrominated diphenyl ether congener 209 (BDE 209) and decabromodiphenyl ethane (DBDPE) were the most abundant brominated flame retardants (BFRs), and tris(chloroisopropyl) phosphate (TCIPP), tris(1,3-dichloroisopropyl) phosphate (TDCIPP), and triphenyl phosphate (TPHP) were the most abundant phosphate flame retardants (PFRs). In bedrooms, the AC filter dust had the highest median levels of BDE 209 (536 ng/g) and DBDPE (2720 ng/g), while bed dust had the highest median levels of ΣPFRs (2750 ng/g) among dust samples. In offices, printer table dust had higher median levels of BDE 209 (1330 ng/g), DBDPE (8470 ng/g), and ΣPFRs (11,000 ng/g) than those in other dust samples. The high dust ingestion values of BDE 209, DBDPE, and individual PFR were 0.28, 1.20, and <0.01-0.32 ng/kg bw/day and 7.37, 31.2, and <0.01-4.54 ng/kg bw/day for BDE 209, DBDPE, and individual PFR for adults and toddlers, respectively. The high dermal exposure values of individual PFR during sleeping were <0.01-0.23 and <0.01-0.36 ng/kg bw/day for adults and toddlers, respectively. More human exposure pathways other than dust ingestion should be considered, such as the dermal contact with beddings and furniture.

Alteration of Diastereoisomeric and Enantiomeric Profiles of Hexabromocyclododecanes (HBCDs) in Adult Chicken Tissues, Eggs, and Hatchling Chickens.

The concentrations and enantiomer fractions (EFs) of α-, ß-, and γ-hexabromocyclododecanes (HBCDs) were measured in chicken diet sources (soil and chicken feed), home-raised adult chicken (Gallus domesticus) tissues, eggs during incubation, and hatchling chicken tissues. HBCD concentrations were not detected-0.69 ng/g dry weight (dw) and 25.6-48.4 ng/g dw in chicken feed and soil, respectively. HBCDs were detected in all adult chicken tissues, except the brain, at median levels of 13.1-44.0 ng/g lipid weight (lw). The proportions of α-HBCD in total HBCDs increased from 51% in soil to more than 87% in adult chicken tissues. The accumulation ratios (ARs) of α-HBCD from diet to adult chicken tissues were 4.27 for liver, 11.2 for fat, and 7.64-12.9 for other tissues, respectively. The AR and carry-over rate (COR) of α-HBCD from diet to eggs were 22.4 and 0.226, respectively. The concentrations of α-HBCD in hatchling chicken liver (median: 35.4 ng/g lw) were significantly lower than those in hatchling chicken pectoral muscle (median: 130 ng/g lw). The EFs of α-HBCD decreased from soil to adult chicken tissues and from eggs to hatchling chicken liver. Meanwhile, the EFs of γ-HBCD increased from soil to adult chicken tissues. These results indicate the preferential enrichment of (-)-α-HBCD and (+)-γ-HBCD in chickens. The alteration of diastereoisomeric and enantiomeric patterns of HBCDs might be influenced by the different absorption and elimination rates of the six HBCD enantiomers as well as variations in HBCD metabolism in chickens.

Bioaccumulation of short chain chlorinated paraffins in a typical freshwater food web contaminated by e-waste in south china: Bioaccumulation factors, tissue distribution, and trophic transfer.

Short chain chlorinated paraffins (SCCPs) are under review for inclusion into the Stockholm Convention on Persistent Organic Pollutants. However, limited information is available on their bioaccumulation and biomagnification in ecosystems, which is hindering evaluation of their ecological and health risks. In the present study, wild aquatic organisms (fish and invertebrates), water, and sediment collected from an enclosed freshwater pond contaminated by electronic waste (e-waste) were analyzed to investigate the bioaccumulation, distribution, and trophic transfer of SCCPs in the aquatic ecosystem. SCCPs were detected in all of the investigated aquatic species at concentrations of 1700-95,000 ng/g lipid weight. The calculated bioaccumulation factors (BAFs) varied from 2.46 to 3.49. The relationship between log BAF and the octanol/water partition coefficient (log KOW) for benthopelagic omnivorous fish species followed the empirical model of bioconcentration, indicating that bioconcentration plays an important role in accumulation of SCCPs. In contrast, the relationship for the benthic carnivorous fish and invertebrates was not consistent with the empirical model of bioconcentration, implying that the bioaccumulation of SCCPs in these species could be more influenced by other complex factors (e.g., habitat and feeding habit). Preferential distribution in the liver rather than in other tissues (e.g., muscle, gills, skin, and kidneys) was noted for the SCCP congeners with higher log KOW, and bioaccumulation pathway (i.e. water or sediment) can affect the tissue distribution of SCCP congeners. SCCPs underwent trophic dilution in the aquatic food web, and the trophic magnification factor (TMF) values of SCCP congener groups significantly correlated with their corresponding log KOW values (p < 0.0001). The present study results improved our understanding on the environmental behavior and fate of SCCPs in aquatic ecosystem.

Tracing the biotransformation of polychlorinated biphenyls (PCBs) in common carp (Cryprinus carpio): Enantiomeric fraction and compound-specific stable carbon isotope analyses.

Metabolites of polychlorinated biphenyls (PCBs) in fish are difficult to detect in vivo due to the complexity of biometabolism. In the present study, atropisomeric fraction analysis of chiral PCB congeners and compound-specific isotopic analysis (CSIA) were applied to trace the biotransformation of PCBs in fish by exposure of common carp (Cryprinus carpio) to the commercial PCB mixture Aroclor 1242. Stereoselective elimination of the chiral PCB congeners 91, 95, and 136 was observed, indicating a stereoselective biotransformation process. The δ(13)C values of PCBs 5/8, 18, and 20/33 in fish were increased compared with those in the spiked food, while PCBs 47/48 and 49 showed significant heavy isotope depletion. These results suggested a significant biotransformation of the corresponding individual PCB congeners although the potential PCB metabolites, hydroxylated PCBs (OH-PCBs) and methylsulfone PCBs (MeSO2-PCBs), were not detected in the fish tissue samples throughout this experiment. The results of the present study demonstrated that a combination of chiral analysis and CSIA is a promising new approach for investigating the biotransformation of PCBs in biota.