Polychlorinated Biphenyls Homologues Research Articles

Enhanced biodegradation of polychlorinated biphenyls by co-cultivation of resuscitated strains with unique advantages

The investigation into viable but non-culturable (VBNC) bacteria through the implementation of resuscitation promoting factors (Rpfs) has broadened the potential sources for isolating strains capable of degrading polychlorinated biphenyls (PCBs). Nonetheless, there has been limited research on the efficacy of resuscitated strains and the potential improvement of their performance through co-cultivation. In this work, the PCB degradation potential of resuscitated strains, specifically Pseudomonas sp. HR1 and Achromobacter sp. HR2, as well as their co-cultures, was investigated. Of particular importance was the comparative analysis between the optimal co-culture and individual strains regarding their ability to degrade PCB homologs and mineralize intermediate metabolites. The results suggested that the resuscitated strains HR1 and HR2 demonstrated robust growth and effective degradation of Aroclor 1242. The co-culture CO13, with an optimal HR1 to HR2 ratio of 1:3, exhibited a remarkable improvement in PCB degradation and intermediate metabolite mineralization compared to individual strains. Analysis of functional genes and degradation metabolites revealed that both the individual strains and co-culture CO13 degraded PCBs via the HOPDA-benzoate pathway, then mineralized through protocatechuate meta- and ortho-cleavage pathways, as well as the catechol ortho-cleavage pathway. This study represents the first documentation of the improved PCB degradation through the co-cultivation of resuscitated strains, which highlights the great promise of these resuscitated strains and their co-cultures as effective bio-inoculants for enhanced bioremediation.

Centurial deposition records of polychlorinated biphenyls and organochlorine pesticides in sediment cores from a plateau deep-water lake of China: Significance of anthropogenic impacts, transformation signals and ecological risks revealed by full congener analysis

Lake Fuxian, the largest deep freshwater lake in China, has been suffering from increasing ecological and environmental issues along with the rapid urbanization and industrialization in the past 40 years. To better understand the historical pollution of persistent organic pollutants (POPs) in Lake Fuxian, comprehensive analyses of 209 polychlorinated biphenyl (PCB) congeners and 20 organochlorine pesticides (OCPs) were conducted in two intact sediment cores (Core V1 and Core V2). The total mass concentrations of PCBs ranged from 7.60 to 31.47 ng/g (dry weight basis) and 5.55 to 28.90 ng/g during the period of 1908–2019 in Core V1 and 1924–2019 in Core V2, respectively. PCBs exhibited a consecutive increasing trend from 1940s to 2019 in Core V1. The temporal trend of PCBs in Core V2 basically matched to the history of PCB usage and prohibition in China (increasing from 1940s to mid-1960s, a remarkable drop in mid-1970s, and then increasing until 2019). Moreover, low-chlorinated PCBs were dominant among PCB homologues. Mono-CBs, di-CBs, tri-CBs and tetra-CBs accounted for 86.71 %–98.57 % in sediment segments. The PCB sources included unintentional emission and atmospheric deposition, as well as biological transformation. The total mass concentrations of OCPs ranged from 0.74 to 3.82 ng/g in Core V1 and 0.35 to 2.23 ng/g in Core V2, respectively. Similar trend was observed in the two sediment cores with peaks in the early 1990s. The predominant OCPs were γ-hexachlorohexane (γ-HCHs), dieldrin and p,p′-DDD. The ecological risks posed by PCBs and p-p′-DDD in Lake Fuxian were relatively low. In contrast, dieldrin might pose a potential threat to exposed organisms and apparently adverse ecological effects were caused by γ-HCH. This study will provide important baseline information on historical POPs contamination of Lake Fuxian.

Evaluation of Polychlorinated Biphenyls in Sediments from Surface Waters of Igodan, Okunmo, Lebi, Idepe and OAUSTECH in Okitipupa, Ondo State Nigeria

The presence of PCBs in water bodies is an emerging issue for water quality. This is because, once PCBs reach a lake or river, they concentrate in the sediments by attaching to the organic matter. Therefore, the objective of this paper is to evaluate the level of polychlorinated biphenyls (PCBs) in sediment from surface waters of Igodan, Okunmo, Lebi, Idepe and Oaustech in Okitipupa, Ondo State Nigeria using appropriate standard methods. Data obtained reveals that in Igodan the concentration of PCBs in sediment w.as PCB 44 (5.42±0.00), PCB 18 (3.04±0.00), PCB 28 (3.27±0.07) and PCB 170 (6.60±0.00). Okunmo PCBs concentration in sediment was PCB 44 (0.67±0.00), PCB 18 (0.03±0.00), PCB 28 (0.32±0.00) and PCB 170 (0.18±0.00). Lebi PCBs concentration in Sediment was PCB 44 (0.82±0.00), PCB 18 (3.96±0.00), PCB 28 (1.12±0.00) and PCB 170 (1.08±0.00). Except for PCB 170 (0.33±0.02), the PCB concentration in sediment from the Idepe and the OAUSTECH were both below the detection limit (BDL). Correlation between Physicochemical Parameters and PCBs homologs shows a negative correlation for the relationship of EC (Electrical Conductivity), TOC (Total Organic Carbon) and pH at ( -0.283), (-0.262) and ( -0.246) respectively. According to multivariate investigation, releases from nearby factories, deterioration of electrical cables and transformers, waste from university laboratories and facilities, as well as diesel residues from lister engines could be associated with the elevated levels of PCBs in sediments collected from the five sampled sites in Ondo State. TriPCBs > tetraPCBs were in this order in which the median concentrations of PCB homologues were found in sediments from the surface water.

Polychlorinated biphenyls (PCBs) in intertidal sediment and water from Lagos lagoon: Baseline report on occurrence, distribution and ecotoxicological risk assessment

To assess the occurrence and potential ecological risk associated with organic micropollutants in Lagos lagoon, 27 polychlorinated biphenyls (PCBs) were analysed in sediments and surface water. Sediment samples were obtained from 18 designated sites (SD1 – SD18) using a Van Veen grab sampler and extracted following standard procedures. Cleaned extracts were analysed using gas chromatography with electron capture detector (ECD). The concentration of ∑PCBs in sediment samples ranged between 6757.61 and 273.46 µg/kg. The PCB homologues distribution patterns in sediments indicated that the low-chlorinated (∑di-PCB - ∑penta-PCB) PCBs were more dominant with 61.1 % occurrence than the high-chlorinated ((∑hexa-PCB - ∑nona-PCB) PCBs with 38.9 % relative abundance. The following is the decreasing order of the average homologue composition of PCBs in sediment samples: ∑tetra-PCB (24.6%) > ∑octa-PCB (21 %) > ∑hexa-PCB (13.8 %) > ∑penta-PCB (12.8) > ∑tri-PCB (11.4 %) > ∑hepta-PCB (7.8 %) > ∑nona-PCB (4.9 %) > ∑di-PCB (2.9 %). More so, the ∑PCBs in surface water samples ranged from 69.28 to 440.90 ng/L, with the mean ranging between 7.21 and 16.33 ng/L. The class distribution of PCB homologue profiles in water samples indicated that highly-chlorinated (∑hexa-PCB to ∑nona-PCB) PCBs were the dominant homologues, with 94.4 % occurrence, compared to the very low occurrence rate (5.6 %) of the low-chlorinated (∑di-PCB to ∑penta-PCB) PCBs. Hexa-PCBs (PCB-138 and PCB-153) were the dominant congeners in most water samples. The concentrations of ∑PCBs in sediments and surface water were unprecedentedly high at almost all locations. The total toxicity equivalent concentrations (TTECs) of dioxin-like PCBs for the sediment samples ranged from 0.001 to 2.43 µg/kg, with an average of 0.34 µg/kg. These findings suggest that PCB congeners are pervasive from anthropogenic point sources of pollution. Intensive site-specific monitoring and remediation are recommended.

Seasonal Air–Sea Exchange Dynamics of Polychlorinated Biphenyls Over the East China Marginal Seas: The Role of Water Masses in a Complex Coastal–Ocean Current System

AbstractContinental marginal seas are key reservoirs of anthropogenic pollutants. Understanding the physical processes controlling the air–sea exchange dynamics of polychlorinated biphenyls (PCBs) in the continental margin seas is crucial to constrain the contribution of PCBs from land and rivers to the ocean; however, the transport and fate of PCBs, and their controlling factors of air–sea exchange in the continental marginal seas still remain poorly understood. Here, we collected atmospheric and surface water samples from the Yellow Sea (YS) and East China Sea (ECS) in summer 2018 and winter 2019, and examined the PCB concentrations. The PCB air–sea gas exchange fluxes showed higher net volatilization in winter, largely due to southward movement of the strengthened Yellow Sea Coastal Current and Yangtze River Diluted Water with high PCB concentrations. Both the dissolved PCB concentrations in seawater and wind speed were the primary factors influencing the PCB air–sea exchange fluxes in winter. By contrast, weak PCB volatilization fluxes occurred when the Taiwan Warm Current with low PCB concentrations dominated in the ECS in summer. In comparison, the accumulation and release of some PCB homologues caused by a green tide in the coastal YS could lead to increased volatilization flux in summer. Our results suggest the transfer of air–sea exchange dynamics of PCBs from a water concentration‐dominated pattern to an environmental parameter‐controlled one due to their decreased land‐based input, and highlight the impact of water mass‐triggered changes (environmental parameters and algal blooms) on the air–sea exchange behavior of PCBs in the continental marginal sea.

Assessment of Polychlorinated Biphenyls and Their Hydroxylated Metabolites in Postmortem Human Brain Samples: Age and Brain Region Differences.

Exposure to polychlorinated biphenyls (PCBs) and their hydroxylated metabolites (OH-PCBs) has been implicated in neurodevelopmental disorders. However, the distribution of PCBs and OH-PCBs in the human brain has not been characterized. This study investigated the age-, sex-, and brain region-specific distribution of all 209 PCBs using gaschromatography–tandem mass spectrometry (GC–MS/MS) in neonatal (N = 7) and adult (N = 7) postmortem brain samples. OH-PCB analyses were performed by GC–MS/MS (as methylated derivatives) and, in a subset of samples, by nontarget liquid chromatography high-resolution mass spectrometry (Nt-LCMS). Fourteen higher chlorinated PCB congeners were observed with a detection frequency >50%. Six lower chlorinated PCBs were detected with a detection frequency >10%. Higher chlorinated PCBs were observed with higher levels in samples from adult versus younger donors. PCB congener profiles from adult donors showed more similarities across brain regions and donors than younger donors. We also assess the potential neurotoxicity of the PCB residues in the human brain with neurotoxic equivalency (NEQ) approaches. The median ΣNEQs, calculated for the PCB homologues, were 40-fold higher in older versus younger donors. Importantly, lower chlorinated PCBs made considerable contributions to the neurotoxic potential of PCB residues in some donors. OH-PCBs were identified for the first time in a small number of human brain samples by GC–MS/MS and Nt-LCMS analyses, and all contained four or fewer chlorine.

Uptake of PCBs into sediment dwellers and trophic transfer in relation to sediment conditions in the Salish Sea

We examined uptake of polychlorinated biphenyls (PCBs) into various marine sediment feeders relative to physical and geochemical factors and transfer to higher trophic levels. PCBs exceeding Canadian Council Ministers of the Environment Guidelines by 6–55× were found in industrialized harbours and some near-outfall sediments, indicating ongoing land input. Sediment PCBs were correlated with organic flux and content. Tissue PCBs were >10× sediment PCBs in all samples and highest in Victoria Harbour infauna, suggesting considerable uptake from these extremely contaminated, organically enriched, chronically disturbed sediments. Sediment PCBs were the primary predictor of tissue lipid PCBs followed by %fines. This results in generally higher tissue PCBs in more depositional regions. The lipid/sediment PCBs (uptake rate) declined with increasing sediment PCBs, acid volatile sulfides and benthos biomass turnover. PCB homologue composition did not change with uptake from sediments or at higher trophic levels, suggesting minimal metabolization in tissues. Trophic bio-magnification occurs since lipid PCBs were 2–100× higher in seal blubber than sediment feeders. PCBs were compared with polybrominated diphenyl ethers (PBDEs) for the same samples. PCBs were highest in industrialized harbours, whereas PBDEs were elevated in harbours but highest near wastewater discharges. This reflects differences in usage history, sediment dynamics, and affinities. PCBs appear to be more bio-accumulative and persistent at higher trophic levels than PBDEs.

Improving the Adsorption Efficiencies of Polychlorinated Biphenyls and Polybrominated Diphenyl Ethers Using a Passive Water Sampling Device in Marine Environment

This study focused on improving the adsorption efficiencies of organic micropollutants, such as polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) using a passive water sampling device (PWSD) in a marine environment during summer. Two factors were considered when increasing the adsorption efficiency by improving the sampling rate (Rs) of PWSDs for target PCBs and PBDEs: 1. Controlling the invasion of the sticky organisms that cause biofouling by tearing the semipermeable membrane device (SPMD) inside the PWSD canister; 2. Preventing various suspended solids from clogging the PWSD pores. To resolve these problems, two types of enhanced PWSD samplers were devised, namely a round prest-type PWSD canister with zooplankton netting (netted), and a copper-coated prest-type PWSD canister. Copper is generally toxic to marine organisms. The netted and copper-coated PWSD samplers were deployed in Masan Bay and Ulsan Bay and their adsorption efficiencies for PCBs and PBDEs were compared with that of the prest-type PWSD sampler. The copper-coated PWSD had an Rs 1.5~1.8 times higher than that of the netted and prest-type PWSDs. A comparison of the adsorption amount of PCBs and PBDEs showed similar results, and copper-coated PWSD adsorbed more target compounds than the netted and prest-type PWSDs. The adsorption patterns of PCB homologues were similar regardless of the sampling site and sampler type, but those of PBDE homologues in the netted and prest-type PWSDs deployed in Ulsan Bay were somewhat different from the others. By comparing the adsorption amounts of PCB and PBDE homologues according to the octanol-water partition coefficients, it was found that the coppercoated PWSD adsorbed more PCBs and PBDEs than the netted and prest-type PWSDs, especially high molecular homologues. Based on these results, the copper-coated PWSD could be used to effectively prevent the biofouling of the SPMD membrane and clogging of the PWSD canister during both summer and winter.

Effect of membrane filtration on the fate of polychlorinated biphenyls in wastewater treatment

The Spokane River is impacted by levels of polychlorinated biphenyls (PCBs) that have triggered fish consumption advisories and exceed water quality standards. Select wastewater treatment plants (WWTPs) on the river have been upgraded from secondary (biological) treatment to tertiary treatment in the form of membrane filtration to address phosphorus contamination. Because membrane filtration is effective at removing particles, it is likely to reduce PCB concentrations in the effluent as well. In this work, PCBs measured in the influents and effluent of several WWTPs discharging to the river were examined. Implementation of membrane filtration reduced PCB concentrations in the effluent (and therefore PCB loads to the river) by 33% at a facility that produces recycled and virgin paper and by ∼55% at municipal WWTPs, compared to secondary (activated sludge) treatment. Largest reductions in concentrations in effluent and loads were achieved for higher molecular weight (MW) PCB congeners (i.e. those with six or more chlorines), homologs, and formulations. The more modest reductions in effluent concentrations achieved at the paper WWTP may be due to the mix of PCBs in the wastewater there: it contained primarily the low MW Aroclor 1242 (presumably from carbonless copy paper) and PCB 11 (3,3′-dichlorobiphenyl) possibly from pigments. PCBs that appear to be associated with silicone products such as caulk, tubing, and o-rings are relatively more abundant in the effluent of some plants compared to the influent, suggesting that these congeners arise from contamination during sampling or from within the plant itself. At some WWTPs, this contamination accounts for nearly a third of PCBs measured in the effluent.

Concentrations, sources, and exposure risk of polychlorinated biphenyls in soil profiles of the floodplain of the lower reaches of the River Niger, Nigeria.

The concentrations of 28 polychlorinated biphenyls (PCBs) were determined in soils collected at three depths from thirteen different sites along the floodplain of the lower reaches of the River Niger (LRRN) in Nigeria. The aim of the study was to provide data on the levels of contamination, sources of the contaminants, and risks to the ecosystem and humans. Soil samples were Soxhlet extracted with a solvent mixture of dichloromethane (DCM)/n-hexane and cleaned up on a column packed with Florisil and silica gel. The PCBs in the samples were quantified by gas chromatography-mass spectrometry. The Ʃ28 PCB concentrations in the floodplain soils varied between not detected (nd) and 11,151ngg-1 for different sampling sites and depths. The PCB concentrations and homologue distribution patterns in soil profiles of the floodplain of the LRRN showed remarkable differences with respect to sites and depths. The results obtained were used to evaluate the ecological and human health risks, which indicated that there is a potential risk to organisms and humans from exposure to PCBs in these soil profiles. The source evaluation as determined by principal component analysis suggested that PCBs in these soil profiles came from burnt circuit boards, cable wires, use of paints, discharges from transformers, long-range migration, and deposition.

Leaching characteristics and hazard evaluation of bottom ash generated from common biomedical waste incinerators

India has more than 202 biomedical waste incinerators, however, knowledge on the chemical characteristics of incinerator ash is lacking. The objective of this study was to evaluate the lecahablility characteristics of bottom ash and to study the levels of incineration by-products viz. polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs). Bottom ash samples from 13 common biomedical waste treatment facilities (CBMWTF) were colleted and subjected to leachig test, sequential extraction procedure (SEP) and PAHs and PCBs analysis. Among metals, cadmium, chromium, manganese, lead and zinc were found higher than the regulatory limits indicating its hazardous nature. SEP showed that substantial fraction of Cd (30%) and Zn (25%) were associated with leachable fractions, whereas metals such as Cr, Fe, Mn, and Ni were mainly associated with reducible, organics and residual fractions. Concentrations of USEPA 16 priority PAHs ranged between 0.17–12.67 mg kg−1 and the total toxic equivalents (TEQ) were in the range of 0.9–421.9 ng TEQ/g. PAHs with 4-rings dominated all the samples and accounted for 68% to total PAHs concentrations. Concentration of Σ19 PCB congeners ranged from 420.4 to 724.3 µg kg−1. PCBs homologue pattern was dominated by mono- to tetra chlorinated congeners (60–86%). The findings indicate the need for segregation of plastics from biomedical waste, improvement of combustion efficiency, and efficient air pollution control devices for the existing incinerators in CBMWTFs.

Accumulation characteristics and estimated dietary intakes of polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans and polychlorinated biphenyls in plant-origin foodstuffs from Chinese markets

The levels and accumulation characteristics of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polychlorinated biphenyls (PCBs) were investigated in nine pools of representative plant-origin foodstuffs randomly collected from markets located in five regions of the Chinese mainland during 2018–2019. The collected foodstuffs consisted of cereals, beans, potatoes, leafy vegetables, root and stem vegetables, melon vegetables, legume vegetables, edible fungi, and mixed vegetable oil. In the fresh plant food pools, the concentrations of toxic equivalency (WHO-TEQ) were in the ranges of 0.9–14.5 pg/kg in upperbound (UB) scenario and 0.002–7.3 pg/kg in lowerbound (LB) scenario on a fresh weight basis; and TriCDFs and TeCBs were the predominant PCDD/F and PCB homologues, respectively. In the mixed vegetable oil, the WHO-TEQ concentrations were 129.4 pg/kg and 103.6 pg/kg on a lipid weight basis in UB and LB scenarios, respectively; and high-chlorinated PCDD/F and PCB homologues were much more abundant. The estimated plant food-borne dietary intakes of WHO-TEQ by a standard adult in the five surveyed regions were in the ranges of 3.39–4.20 and 1.57–2.13 pg WHO-TEQ/kg body weight/month in UB and LB scenarios, respectively. Among all surveyed regions, consumption of cereals and vegetable oil made up the primary contributions to the estimated dietary intakes of WHO-TEQ. TriCDFs accounted for 41.1–83.9% of the PCDD/Fs dietary intakes via consumption of plant foods, and TeCBs made up 61.2–73.0% of the PCBs dietary intakes via consumption of plant foods, suggesting that the potential toxic effects of TriCDFs and TeCBs on human health should be concerned.

Municipal waste landfill as a source of polychlorinated biphenyls releases to the environment.

This study aimed to investigate the impact of municipal waste landfill on polychlorinated biphenyls (PCBs) release to the environment concerning groundwater flow directions. The contents of polychlorinated biphenyls in soils, plants and water were analysed at various distances from the landfill. Thanks to low solubility PCBs in water groundwater flow direction, under the landfill, have an influence on PCBs concentration in groundwater. Strong PCBs’ sorption to organic matter caused that no affect groundwater flow directions on PCB content in soils and plants’ tissues was observed. The largest PCBs deposition zone was located 50 m from the contamination source (landfill). Tri-CB and tetra-CB homologues were capable of migration deep into the soil profile, which could be related to the geological material from which the soils under study were developed, as well as to the properties of the PCB homologues.

Distribution characteristics and environmental fate of PCBs in marine sediments at different latitudinal regions: Insights from congener profiles

Sediments were sampled from Hangzhou Bay (HB), the South China Sea (SCS), and Antarctica (AZ) to better understand the distribution characteristics and environmental fate of polychlorinated biphenyls (PCBs) at different latitudes. Numerous PCB congeners (68) were detected among the sampling sites, supporting the ubiquity of PCB congeners. High and low chlorinated congeners dominated the PCB profiles of AZ and SCS, respectively, whereas the PCB homologues were evenly distributed in the HB. As a fraction of low chlorinated PCBs originates from an exogenous input, the low mean ratios of ∑Tetra-CBs to ∑PCBs and ∑Tetra-CBs to the sum of ∑Tri- and ∑Di-CBs suggest that microbial transformation of PCBs is weak in marine surface sediments, if any occurs at all. Furthermore, PCB contamination levels in marine sediments may be primarily influenced by latitude rather than pollution sources. Thus, the findings of this study suggest that Antarctica is becoming a prospective hotspot for PCBs.

Spatial characteristics and risk assessment of polychlorinated biphenyls in surficial sediments around crude oil production facilities in the Escravos River Basin, Niger Delta, Nigeria

In this study, the concentrations of 28 polychlorinated biphenyl (PCB) congeners, including 12 dioxin-like PCBs and 7 indicator PCBs, were determined in sediments around oil production facilities in the Escravos River Basin of the Niger Delta in Nigeria. The aim was to describe the spatial patterns, sources, and ecosystem risks associated with exposure to PCBs in sediments of this river basin. Gas chromatography-mass spectrometry (GC–MS) was used to determine the concentrations of PCBs in the sediments. The Ʃ28 PCB concentrations in sediments from the Escravos River Basin ranged between 226 and 31,900 ng g−1 with a median concentration of 2300 ng g−1. The results indicated that sediments around crude oil production facilities, such as, wellheads, flow stations, and truck lines, had significantly higher levels of Ʃ28 PCBs (p < 0.05) than those collected near residential communities within the river basin. The median concentrations of PCB homologues in sediments from this river basin followed the sequence: hexaPCBs > penta-PCBs > tetra-PCBs > hepta-PCBs > tri-PCBs > di-PCBs > deca-PCBs > octa-PCBs > nona-PCBs. The risk assessment of PCBs in sediments from this river basin suggest very high potential risks for both organisms and humans.

Passive sampler derived polychlorinated biphenyls (PCBs) in indoor and outdoor air in Bursa, Turkey: Levels and an assessment of human exposure via inhalation

Although polychlorinated biphenyls (PCBs) were banned several years ago, they can still be measured in the environment, especially in indoors, where their concentrations tend to be higher than outdoors in some cases. The current study reports the results of a study conducted to determine concentrations of a total of 40 PCBs congeners in the living rooms and kitchens of eight different houses, and in the outdoor air of three houses during summer and autumn in Bursa in 2014. The province of Bursa, having eighteen of organized industrial zones, indoor air pollution is of great importance. The average concentration of ∑40PCBs in living rooms and the kitchen were 604 ± 210 pg/m3 and 639 ± 2514 pg/m3 during summer, respectively; while concentrations in autumn were 362 ± 167 pg/m3 and 309 ± 93 pg/m3, respectively. The average ∑40PCBs outdoor concentrations were 303 ± 183 pg/m3 and 41 ± 23 pg/m3 for summer and autumn, respectively. The ∑40PCBs concentrations in summer were almost two times higher than in autumn for indoor environment. The predominant PCB homologs in indoor samples were penta- (40%), tetra- (23%) and tri-CBs (17%) while they were penta- (37%) and tetra-CBs (22%) for outdoor samples. The results of the study indicated the presence of intentionally and unintentionally produced PCBs. The I/O ratios suggested the indoor sites as the most important PCBs source than outdoor sites. Finally, the measured PCB concentrations did not represent a cancer risk for human health for exposure via inhalation in all sampling points.

Tissue Distribution and Immunomodulation in Channel Catfish (Ictalurus punctatus) Following Dietary Exposure to Polychlorinated Biphenyl Aroclors and Food Deprivation.

Although most countries banned manufacturing of polychlorinated biphenyls (PCBs) over 40 years ago, PCBs remain a global concern for wildlife and human health due to high bioaccumulation and biopersistance. PCB uptake mechanisms have been well studied in many taxa; however, less is known about depuration rates and how post-exposure diet can influence PCB concentrations and immune response in fish and wildlife populations. In a controlled laboratory environment, we investigated the influence of subchronic dietary exposure to two PCB Aroclors and food deprivation on tissue-specific concentrations of total PCBs and PCB homologs and innate immune function in channel catfish (Ictalurus punctatus). Overall, we found that the concentration of total PCBs and PCB homologs measured in whole body, fillet, and liver tissues declined more slowly in food-deprived fish, with slowest depuration observed in the liver. Additionally, fish that were exposed to PCBs had lower plasma cortisol concentrations, reduced phagocytic oxidative burst activity, and lower cytotoxic activity, suggesting that PCBs can influence stress and immune responses. However, for most measures of immune function, the effects of food deprivation had a larger effect on immune response than did PCB exposure. Taken together, these results suggest that short-term dietary exposure to PCBs can increase toxicity of consumable fish tissues for several weeks, and that PCB mixtures modulate immune and stress responses via multiple pathways. These results may inform development of human consumption advisories and can help predict and understand the influence of PCBs on fish health.

Occurrence and risk evaluation of organochlorine contaminants in surface water along the course of Swartkops and Sundays River Estuaries, Eastern Cape Province, South Africa.

Organochlorine contaminants were analysed in surface water from Sundays (SDE) and Swartkops Estuaries (SWE), Eastern Cape Province, which is among the largest estuaries in South Africa. The concentration of Σ18OCPs ranged from 16.7 to 249.2ng/L in autumn, 19.9-81.4ng/L in winter, 43.6-126.8ng/L in spring and 68.3-199.9ng/L in summer for SDE, whereas in SWE, the values varied from 20.9 to 259.7ng/L in autumn, 58.9-263.9ng/L in winter, 3.2-183.6ng/L in spring and 118.0-188.9ng/L in summer. Among all OCPs, α-HCH, β-HCH, p,p'-DDE, p,p'-DDT, endrin, dieldrin and endrin aldehyde were predominant in surface water samples from SDE and SWE. Furthermore, the mean concentration of polychlorinated biphenyls (PCBs) ranged from 126.7ng/L in winter to 151.0ng/L in spring for SDE and 249.0ng/L in spring to 727.6ng/L in winter for SWE. Tri- and tetra-PCBs dominated the PCB homologue profile. Hierarchical cluster analysis grouped the study sites into three regions from least polluted to most polluted, indicated that SWE is more polluted compared to SDE, probably due to the influx of agricultural and industrial effluents. Carcinogenic and non-carcinogenic risk assessment revealed that the water from both estuaries is not safe for drinking, although suitable for bathing.

Polybrominated diphenyl ethers and polychlorinated biphenyls in indoor dust from electronic repair workshops in southern Nigeria: Implications for onsite human exposure

The concentrations of 9 polybrominated diphenyl ethers (PBDEs) and 28 polychlorinated biphenyls (PCBs), including the 7 indicator PCBs and 12 dioxin-like PCBs, were determined in indoor dusts from electronic repair workshops in southern Nigeria. The study was aimed at providing information on the distribution and compositional patterns of PBDEs and PCBs in electronic repair workshop dusts as well as evaluating the human exposure risk to these compounds via non dietary ingestion, inhalation and dermal contact pathways. The PBDEs and PCBs in the electronic repair workshop dusts were extracted with a mixture of hexane/acetone by ultrasonication, and the extracts were purified with a multilayer silica gel/alumina column. The PBDEs and PCBs in the purified extracts were determined by means of gas chromatography-mass spectrometry. The concentrations of the PBDEs ranged from 14 to 2578 ng g−1 with a prevalence of 85 to 95% for BDE-28, BDE-47, BDE-99 and BDE-100. The hazard indices for PBDEs were >1 for exposure to dust from television/radio/stereo repair workshops whereas the total cancer risk values were within the acceptable range of 10−6 to 10−4. The Σ28 PCB concentrations ranged from 96.6 to 3949 ng g−1. The PCB compositional patterns indicate that hexa-PCBs are the most prevalent PCB homologues in the electronic repair workshop dusts. The TEQ for the dl-PCBs in the electronic repair workshop dusts ranged from 2.40 to 4.31 g−1. The estimated hazard indices and cancer risk values suggest that there is a substantial risk (carcinogenic and non-carcinogenic) associated with human exposure to PCBs in dusts from these electronic repair workshops. The principal component analysis results indicate that the PCBs in the electronic repair workshop dusts arise from inputs from the technical mixtures of Aroclor 1252, Aroclor 1254 and Aroclor 1260.

Levels and fingerprints of chlorinated aromatic hydrocarbons in fly ashes from the typical industrial thermal processes: Implication for the co-formation mechanism

Municipal solid waste incineration (MSWI) and iron and steel making plants are two of important sources of chlorinated aromatic hydrocarbons (CAHs). In this study, the typical CAHs including polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs), polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs) and chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs) in fly ash samples collected from MSWI, iron ore sintering (IOS) and steel smelting (SS) plants were simultaneously identified and quantified. The total concentrations of quantified CAHs in different fly ashes showed a large variation (5.88-4255 ng/g). Cl-PAHs were found to be predominant CAH species in most of fly ash samples, and the concentrations of mono-chlorinated PAHs in all fly ashes were obviously higher than those of di-chlorinated PAHs. The fingerprints of CAHs in MSWI fly ashes were mainly characterized by the high content of PCDDs, especially the hexa-CDD homologue. However, in IOS and SS fly ashes, tetra- to hexa-CDF homologues showed the higher abundance, and tetra-to octa-CDFs predominated over tetra- to octa-CDDs by factors of 3-26. The strong concentration correlations were observed between tetra- to octa-CDF homologues, middle-chlorinated PCN and PCB homologues, between tetra- to octa-CDD homologues, between low-chlorinated PCB and PCN homologues, between di-chlorinated PAH homologues, and between deca-CB and highly chlorinated PCN homologues. These results implied that the main formation mechanism of CAHs might be significantly varied with the change of chlorination degree and aromatic ring structure.