Selected Polychlorinated Biphenyls Congeners Research Articles

Novel Ferrocene-Containing Triacyl Derivative of Resveratrol Protects Ovarian Cells from Toxicity Caused by Ortho-Substituted Polychlorinated Biphenyls

Polychlorinated biphenyls (PCBs) can induce neurotoxicity, immunotoxicity, reproductive toxicity, genotoxicity, and carcinogenicity (IARC group 1 Carcinogens). Scientific data suggest that resveratrol possesses the ability to attenuate ortho-PCB-induced toxicity. Recently, a novel ferrocene-containing triacyl derivative of resveratrol (RF) was synthesized and in this study, its potential to protect CHO-K1 cells from selected PCB congeners (75 µM) was evaluated. Cell viability/proliferation was observed by Trypan Blue (TB), Neutral Red (NR), Kenacid Blue (KB), and MTT bioassays, ROS formation by fluorescent probes, and the extent of apoptosis by flow cytometry. All applied bioassays confirmed that RF (2.5–100 μM) remarkably improves viability in PCB 153-treated cells with an increase in cell survival almost up to control levels. This effect was not determined after PCB 77 exposure, although ROS formation was decreased at RF ≥ 50 µM. Apoptosis was significant (p < 0.05) for both congeners. In PCB 77-treated cells, RF did not suppress the induction of cell death. The intended protective effect of RF was evident when cells were treated with PCB 153, and this correlates with results obtained for cell viability. Compared to resveratrol, the novel RF showed promising results in terms of improved biological activity and cell protection against PCB 153 toxicity at all concentrations tested.

Ecological and Health Risk Assessment of Polychlorinated Biphenyls in Water and Sediments in Bodo Riverine Area, River State, Nigeria

Concentrations of nine polychlorinated biphenyls (PCBs) were assessed in sediments and water in the Bodo River area, Gokana Local Government of River state Nigeria to assess the risk associated within the region due to the effect of oil spillage and marine pollution. The analytical procedure involved the application of Gas Chromatography coupled with mass spectrometric detection (GC/MS) for identification and quantification of and polychlorinated biphenyls respectively with high degree of accuracy and precision after triplicate analysis. All the selected PCB congeners analyzed were detected in the analyzed samples at different frequencies. The total concentrations of PCBs ranged from nd (not detected) to 4.15 mg/kg in sample A with an average concentration of 1.66 mg/kg, nd to 8.4 mg/kg in sample B with an average concentration of 3.25 mg/kg and nd to 7.30 mg/kg in sample C with an average concentration of 3.64 mg/kg in sediments. While the total concentrations of PCBs in the water sample ranged from nd (not detected) to 1.25 mg/kg in sample A with an average concentration of 0.56 mg/kg, nd to 4.50 mg/kg in sample B with an average concentration of 1.20 mg/kg and nd to 2.2 mg/kg in sample C with an average concentration of 0.88 mg/kg. Health risk assessment employed in this study includes the chronic daily intake and the carcinogenic risk via ingestion, inhalation and dermal contact using established guidelines. The total concentrations of PCBs were used to assess the cancer risk probabilities in humans via ingestion, dermal contact and inhalation of sediments particles. Very low cancer risk was found in all water samples compared to sediments samples caused by ƩPCBs. The results of the ecological risk assessment of PCBs in the Bodo River demonstrated the presence of PCBs in all sampling sites showing that the sites were highly contaminated with largely negative biological effects and a high potential risk to the environment.

Particle/gas partitioning behavior of polychlorinated biphenyls (PCBs) in global atmosphere: Equilibrium or steady state?

Particle/gas (P/G) partitioning governs the atmospheric transport and fate of semi-volatile compounds (SVOCs). Here, we provide a comprehensive investigation of P/G partitioning of polychlorinated biphenyls (PCBs) by comparing the performance of seven models, (including five equilibrium models: Junge-Pankow model, Harner-Bidleman model, Dachs-Eisenreich model, pp-LFER model, mp-pp-LFER model, one empirical Li-Jia model, and one steady-state Li-Ma-Yang model). For this comparison, 5019 monitoring data points from urban, rural and remote sites for PCBs taken from published papers have been accessed, against which the predictions of these models have been evaluated. Among the 5019 monitoring data points, there are 2791 monitoring data for six selected PCB congeners (CB-28 + 31, −52, −101, −153, −180, −207) and 2228 for dozens of other PCB congeners. We find that in predicting the P/G partition quotient (KP) of the six selected PCB compounds, the Li-Ma-Yang model performs best across the entire logKOA (octanol-air partition coefficient) range (from 7.8 to 15.3), with 86 ± 10% of 2791 monitoring data points lying within a deviation of ±1 log unit of the root mean square error (RMSE) of 0.67 ± 0.18 in urban, rural and remote areas. This model is far superior to the other models in predicting KP, especially in the MP Domain (logKOA ≥ 12.50), with 96% of the data points falling within a deviation of ±1 log unit and a RMSE of 0.48, in comparison to the less than 7% for the five equilibrium models and 20% for the empirical Li-Jia model. These findings suggest that when the particle deposition is not negligible, the P/G partitioning of PCBs in ambient atmosphere is not in equilibrium, but in a steady or quasi-steady state. Similar to PBDEs, the properties of individual PCB congeners, such as KOA, are the primary factors affecting the P/G partitioning of PCBs.

Assessment of polychlorinated biphenyls (PCBs) in the Himalayan Riverine Network of Azad Jammu and Kashmir

The emission of polychlorinated biphenyls (PCBs) in South Asian countries is one of the great environmental concerns and has resulted in the contamination of surrounding high altitude regions such as Azad Jammu and Kashmir (AJK), Pakistan. This first investigation of Polychlorinated Biphenyl (PCBs) concentrations in the ambient air, water and surface soil was conducted along the extensive stream network in the AJK valley of the Himalayan Region. In 2014, surface soil samples were taken and passive air and water samplers were deployed along the four main rivers, namely Jhelum, Neelum, Poonch and Kunhar, and analysed for PCBs (33 congeners) using GC-MS/MS. The ∑33PCBs concentrations ranged from 31.17 to 175.2 (mean ± SD: 81 ± 46.4 pg/L), ND to 1908 (1054 ± 588.5 pg/g), and 29.8 to 94.4 (52.9 ± 22.7 pg/m3) in surface water, soil and air matrices, respectively. The levels of dioxin-like PCBs (∑8DL-PCBs) contributed considerably towards the total PCBs concentrations: 60.63% (water), 43.87% (air) and 13.76% (soil). The log transformed air-water fugacity (log fa/fw) ratios ranged from −9.37 to 2.58; with 86.3% of the sampling sites showing net volatilization of selected PCB congeners. Similarly, the fugacity fractions for air-soil exchange exhibited narrow variation (0.8 to < 1) indicating net volatilization of PCBs. The ecological risk assessment showed low potential ecological risks (Eri = 1.58–7.63) associated with PCB contamination. The present findings provide baseline data that suggest cold trapping of POPs in the remote mountainous areas of Pakistan and can support environmental management of POPs at the regional level.This pioneer investigation campaign to assess the PCBs concentrations in Himalayan Riverine Network of Azad Jammu and Kashmir, Pakistan helps to develop baseline data of PCBs from the strategically important riverine environment that would help in future regional as well as global ecological studies. However, the effects of temperature variations on the sampling rates of chemicals across a wide spectrum of volatility along the elevation gradient were not taken under consideration for PCBs atmospheric concentrations.

Occurrence of organochlorine pesticides and polychlorinated biphenyls in sediment and fish in Cau Hai lagoon of Central Vietnam: Human health risk assessment

This is the first study on polychlorinated biphenyls (PCBs) in fish from the Cau Hai lagoon, a part of the largest coastal lagoon in Southeast Asia. Seven selected PCB congeners and organochlorine pesticides in sediments and edible fish tissues were quantified by GC–MS. The sum of ICES-7 PCB and DDTs concentrations in fish species consumed regularly and of economic value were in ranges 26–43 ng g−1 lw and 182–277 ng g−1 lw, respectively. The ratio between the parent DDT compound and the sum of metabolites, DDE and DDD, was most of the time smaller than 1, suggesting primarily an historical contamination of the lagoon. An agglomerative hierarchical clustering indicates sites located in the north-western part of the Cau Hai lagoon were characterized by above-average concentrations of DDE and DDT. Comparing to previous data, a large decrease in ∑DDT residues can be seen over the past 20 years.

Enrichment, isolation and biodegradation potential of psychrotolerant polychlorinated-biphenyl degrading bacteria from the Kongsfjorden (Svalbard Islands, High Arctic Norway)

Persistent organic pollutants (POPs), such as polychlorinated biphenyls (PCBs), have been detected in abiotic Arctic matrices: surface sediments and seawater from coastal areas in the Kongsfjorden were collected and analyzed. Levels of PCBs varied depending on the sampling site. Total PCB concentrations were between 11.63 (site C2W) and 27.69pgl−1 (site AW). These levels were comparable to those reported previously in lake sediments from the northern Svalbard.The occurrence and biodegradation potential of cold-adapted PCB-oxidizing bacteria in seawater and sediment along the fjord was also evaluated. After enrichment with biphenyl, 246 isolates were obtained with 45 of them that were able to grow in the presence of the PCB mixture Aroclor 1242, as the sole carbon source. The catabolic gene bphA was harbored by 17 isolates with affiliates to the genera Algoriphagus, Devosia and Salinibacterium that have been never reported as able to utilize PCBs, thus deserving further investigation. The total removal of Aroclor 1242 and selected PCB congeners was evaluated at 4 and 15°C for eight bphA-harboring isolates and Gelidibacter sp. DS-10. With few exceptions, tested strains showed greater efficiency at 15 than at 4°C. Isolates were able to reduce most chromatographic peaks by >50%, with some di- and trichlorobiphenyls that were quite totally removed (>90%).

Removal of polychlorinated biphenyl congeners in mixture Delor 103 from wastewater by ozonation vs/and biological method

Polychlorinated biphenyls (PCBs) produced in Slovakia as a commercial mixture Delor 103 cause the main contamination of sediment, water and fish in the eastern part of Slovakia. Delor 103 is a mixture of 40% PCB congeners, nine of them: PCB 8 (2,4′-dichlorobiphenyl), PCB 28 (2,4,4′-trichlorobiphenyl), PCB 52 (2,2′,5,5′-tetrachlorobiphenyl), PCB 101 (2,2′,4,5,5′-pentachlorobiphenyl), PCB 118 (2,3′,4,4′,5-pentachlorobiphenyl), PCB 138 (2,2′,3,4,4′,5′-hexachlorobiphenyl), PCB 153 (2,2′,4,4′,5,5′-hexachlorobiphenyl), PCB 180 (2,2′,3,4,4′,5,5′-heptachlorobiphenyl), and PCB 203 (2,2′,3,4,4′,5,5′,6-octachlorobiphenyl), were monitored for their removal by ozonation and biodegradation using Achromobacter xylosoxidans. Ozonation improved the removal of PCB 52, 118, 153, 138, 180, and 203 using biological method with A. xylosoxidans. Degradation of 55% of the total amount of nine selected PCB congeners was achieved by the biological method with A. xylosoxidans, while 86% of the total amount of the nine selected PCB congeners were removed by the ozonation method; using a combination of biological and chemical methods, ozonation and A. xylosoxidans, showed a 94% removal efficiency of the selected PCB congeners present in mixture Delor 103.

Fate and transport of polychlorinated biphenyls (PCBs) in the River Thames catchment – Insights from a coupled multimedia fate and hydrobiogeochemical transport model

The fate of persistent organic pollutants (POPs) in riverine environments is strongly influenced by hydrology (including flooding) and fluxes of sediments and organic carbon. Coupling multimedia fate models (MMFMs) and hydrobiogeochemical transport models offers unique opportunities for understanding the environmental behaviour of POPs. While MMFMs are widely used for simulating the fate and transport of legacy and emerging pollutants, they use greatly simplified representations of climate, hydrology and biogeochemical processes. Using additional information about weather, river flows and water chemistry in hydrobiogeochemical transport models can lead to new insights about POP behaviour in rivers. As most riverine POPs are associated with suspended sediments (SS) or dissolved organic carbon (DOC), coupled models simulating SS and DOC can provide additional insights about POPs behaviour. Coupled simulations of river flow, DOC, SS and POP dynamics offer the possibility of improved predictions of contaminant fate and fluxes by leveraging the additional information in routine water quality time series. Here, we present an application of a daily time step dynamic coupled multimedia fate and hydrobiogeochemical transport model (The Integrated Catchment (INCA) Contaminants model) to simulate the behaviour of selected PCB congeners in the River Thames (UK). This is a follow-up to an earlier study where a Level III fugacity model was used to simulate PCB behaviour in the Thames. While coupled models are more complex to apply, we show that they can lead to much better representation of POPs dynamics. The present study shows the importance of accurate sediment and organic carbon simulations to successfully predict riverine PCB transport. Furthermore, it demonstrates the important impact of short-term weather variation on PCB movement through the environment. Specifically, it shows the consequences of the severe flooding, which occurred in early 2014 on sediment PCB concentrations in the River Thames.

Atmospheric concentrations and loadings of organochlorine pesticides and polychlorinated biphenyls in the Canadian Great Lakes Basin (GLB): Spatial and temporal analysis (1992–2012)

Long-term air monitoring data for POPs are required to determine the effectiveness of source reduction measures and factors controlling air concentrations. Air samples were collected between 1992 and 2012 at three sites with different geographical characteristics (Burnt Island, Egbert and Point Petre) in the Canadian Great Lakes Basin (GLB) using high-volume samplers and analyzed for organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs). Spatial and temporal trends of gas-phase concentrations of OCPs, selected PCB congeners and ƩPCBs (84 congeners) were assessed. Egbert had the highest concentrations of some OCPs due to historical [dichlorodiphenyltrichloroethanes (DDTs), dieldrin, γ-hexachlorocyclohexane (γ-HCH)] and current (endosulfan) applications of these pesticides in the surrounding agricultural cropland. This shows that agricultural areas are a source of OCPs to the GLB. High o,p'-/p,p'-DDT ratios were determined and an increasing trend was observed at Point Petre and Burnt Island up to 2004; indicating that the GLB is influenced by dicofol-type DDT sources, which have higher o,p’-/p,p’-DDT ratios than technical DDT. Atmospheric PCB concentrations at Egbert and Point Petre are higher than those measured at Burnt Island, likely due to urban influence and greater populations. Loadings calculations suggest that the atmosphere is a source of α-endosulfan and p,p’-DDT to the lakes and the opposite is true for p,p’-DDE. Long-term decreasing trends were observed for both OCPs and PCBs; consistent with control measures implemented in North America. Atmospheric PCB concentrations are decreasing relatively slowly, with halflives in the range of 9–39 years. Chlordane, α-endosulfan, β-endosulfan, dieldrin, and DDT-related substances showed halflives in the range of 7–13 years. α-HCH and γ-HCH were decreasing rapidly in air, with halflives of 5 years. Long-term declining trends of PCBs and OCPs suggest that regulatory efforts to reduce emissions to the GLB environment have been effective, but emissions from primary and secondary sources might limit future declines.

The distribution of Polychlorinated Biphenyls (PCBs) in the River Thames Catchment under the scenarios of climate change

Measurements have shown low levels of PCBs in water but relatively high concentrations in the resident fish of the River Thames (UK). To better understand the distribution and behaviour of PCBs in the Thames river basin and their potential risks, a level III fugacity model was applied to selected PCB congeners (PCB 52, PCB 118 and PCB 153). The modelling results indicated that fish and sediments represent environmental compartments with the highest PCB concentrations; but the greatest mass of PCBs (over 70%) is likely to remain in the soil. As emissions decline, soil could then act as a significant secondary source of PCBs with the river bed-sediment functioning as a long-term reservoir of PCBs. The predicted changes in temperature and rainfall forecast in the UK Climate Projections 2009 (UKCP09) over the next 80years had only a modest influence on PCB fate in the model. The most significant result was a tendency for climate change to enhance the evaporation of PCBs from soil to air in the Thames catchment.

Proinflammatory adhesion molecules facilitate polychlorinated biphenyl-mediated enhancement of brain metastasis formation.

Polychlorinated biphenyls (PCBs) are environmental toxicants that cause vascular inflammation and facilitate the development of brain metastases. The crucial event in metastasis formation is adhesion of blood-borne tumor cells to the vascular endothelium, followed by their transcapillary migration. The aim of the present study was to examine the mechanisms of PCB118-induced brain metastasis formation at the blood-brain barrier level with the focus on tumor cell adhesion to the brain endothelium. PCB118 was administered orally to wild-type or intercellular cell adhesion molecule-1 (ICAM-1)-deficient mice, followed by an injection of Lewis lung carcinoma cells into the carotid artery. Treatment with PCB118 resulted in enhanced development of brain metastases. Injection of tumor cells induced overexpression of ICAM-1 and vascular endothelial cell adhesion molecule-1 (VCAM-1) in brain endothelium that was further potentiated in mice exposed to PCB118. PCB118 did not affect the number of adhered and extravasated tumor cells in ICAM-1-deficient mice. Additional in vitro studies indicated that VCAM-1-neutralizing antibody protected against PCB118-induced adhesion of tumor cells to cultured brain endothelial cells. These results indicate that exposure to selected PCB congeners, such as PCB118, induces adhesion and transcapillary migration of tumor cells. This process is facilitated by proinflammatory adhesion molecules and results in potentiation of brain metastasis formation.

Trends in European Background Air Reflect Reductions in Primary Emissions of PCBs and PBDEs

Data are presented for polychlorinated biphenyls (PCBs) and polybrominated diphenyls ethers (PBDEs) in passive air samplers (PAS) collected along a rural/remote latitudinal transect from southern UK to northern Norway during 2004-2008. This study is part of an ongoing campaign, using semipermeable membrane devices (SPMDs) as PAS over two year intervals since 1994. Absolute sequestered amounts of selected PCB congeners have decreased in a first order fashion between 1994-2008, with the average time of 8.4+/-3.2 years for atmospheric concentrations to decline by 50%. PCBs have continued to fractionate with latitude during this period. PBDE concentrations declined by 50% between 2000 and 2008 every 2.2+/-0.4 years. Results are discussed in terms of sources, long-range atmospheric transport, global fractionation, and clearance processes. It is concluded that the spatial and temporal trends in background European air mainly reflect the strength of primary diffusive emissions of these compounds and subsequently their ongoing declines. The direct evidence for this is similar rates of decline at all the sites; similar rates of decline for all congeners; no systematic change in the fractionation pattern since 1994. The latest results indicate a reduction in the rate of decline for PCBs (and hence in primary emissions).

Evaluation of Activated Carbon as a Reactive Cap Sorbent for Sequestration of Polychlorinated Biphenyls in the Presence of Humic Acid

This study investigated the interferences caused by high humic acid concentrations on the adsorption of coplanar and noncoplanar polychlorinated biphenyls (PCBs) on coconut shell activated carbon. In particular, the research focuses on the application of activated carbon as a reactive cap for contaminated sediment sites, a possible intervention to reduce contaminant flux through pore water, and to organisms in aquatic environments. Kinetic and equilibrium studies were conducted using activated carbon as a sorbent for individual PCB congeners including BZ 1, 52, 77, 153, and 169, respectively, in the presence and absence of humic acid. Results showed that preloading of activated carbon with humic acid significantly reduced the adsorption affinity for all selected PCB congeners. Experiments conducted without preloading of activated carbon demonstrated that desorption upon subsequent spiking with humic acid (simulating long-term exposure to pore water that contains high humic acid concentrations) was not found to be statistically significant, and varied with coplanarity of PCBs. Results provide important information for the design of reactive caps in sediments where high concentrations of dissolved organic carbon are found, and highlight the importance of considering site conditions when designing effective reactive caps.

Catalytic Role of Palladium and Relative Reactivity of Substituted Chlorines during Adsorption and Treatment of PCBs on Reactive Activated Carbon

The adsorption-mediated dechlorination of polychlorinated biphenyls (PCBs) is a unique feature of reactive activated carbon (RAC). Here, we address the RAC system, containing a tunable amount of Fe as a primary electron donor coupled with Pd as an electrochemical catalyst to potentially respond to the characteristic of contaminated sites, effectively traps and treats various PCB congeners. A dramatic increase in RAC reactivity with Pd doping at as low as 0.01% suggests its critical role for accelerating hydrodechlorination of PCBs. Characteristic adsorption and dechlorination behavior and ensuing decomposition pathways of 13 selected PCB congeners are discussed with their surface interactions with RAC. Important findings include (i) inherent dechlorination susceptibility of chlorines in para > meta > ortho position, regardless of independent or competitive conditions as well as substrate effects, (ii) favorable reduction of more toxic coplanar PCB congeners, (iii) preferential electrophilic attack to chlorines in a less substituted phenyl ring and an isolated chlorine, regardless of the steric or inductive effect as a dominant limiting factor for the dechlorination of ortho or meta PCBs, respectively, (iv) prominent dechlorination inhibition for higher ortho congeners but negligible inhibition for higher meta congeners, and (v) eventual complete dechlorination of higher PCB congeners to biphenyl.

Contamination profiles of selected PCB congeners, chlorinated pesticides, PCDD/Fs in Antarctic fur seal pups and penguin eggs

The aim of this study was to investigate levels of some major environmental contaminants, such as polychlorinated biphenyls (PCBs), polychlorinated dibenzo- p-dioxins and dibenzofurans (PCDD/Fs) and organochlorine pesticides in Antarctic samples. Concentrations of some persistent organic pollutants (POPs) were investigated in Antarctic fur seal pups and eggs of three species of penguins. Dichloro-diphenyl-trichloroethane (DDT) was the main pollutant, followed by PCBs; other organochlorine compounds such as hexachlorobenzene (HCB) and PCDD/Fs were usually found only in minor quantities. Adélie penguin eggs had significantly higher mean PCB concentrations ( p < 0.05) compared to the other two penguin species, but there was no difference in DDT levels ( p > 0.05). TEQ values in fur seal blubber in our study were one order of magnitude lower than those considered to elicit physiological effects in aquatic mammals. In general, POP concentrations in our samples suggested that likely the study populations were not currently at risk for adverse health effects, but indicated a clear need for further monitoring to assess the presence and time trend of a broad range of contaminants, mainly emerging POPs thought to be increasing in polar regions.

Polychlorinated Biphenyl Levels in Peripheral Blood and Non-Hodgkin's Lymphoma: A Report from Three Cohorts

The incidence of non-Hodgkin's lymphoma (NHL) unrelated to HIV infection has steadily increased over the past several decades and remains substantially unexplained. Limited evidence suggests that increased concentrations of polychlorinated biphenyls (PCB) measured in blood or fat tissue are associated with increased risk of NHL. Although PCB congeners vary in their biological activity, the relation between individual congeners and NHL risk has not been examined previously using prospectively collected biospecimens. We examined congener-specific associations in three prospective cohorts. Prediagnostic serum or plasma concentrations of selected PCB congeners were measured among NHL cases and controls from these cohorts: Janus (190 cases and 190 controls) in Norway and CLUE I (74 cases and 147 controls) and the Nurses' Health Study (30 cases and 78 controls) in the United States. All blood samples were collected in the 1970s or 1980s. We used logistic regression to calculate odds ratios (OR) and 95% confidence intervals (95% CI) for the relations between risk of NHL and lipid-corrected plasma or serum concentrations. Several congeners (i.e., 118, 138, and 153) that were present at higher levels and were moderately to highly correlated with each other showed exposure-response trends with risk of NHL in all three cohorts. These associations were observed primarily among subjects diagnosed closer to the date of blood collection in the two cohorts with sufficient cases to permit stratification by time. Among cases diagnosed within the median years of follow-up (16 years in Janus and 12 years in CLUE I), ORs and 95% CIs for increasing fourths of concentration of congener 118 relative to the lowest fourth were as follows: 2.4 (0.9-6.5), 4.9 (1.6-15.3), and 5.3 (1.5-18.8; P(trend) < 0.005) in Janus and 8.1 (1.0-68.9), 6.6 (0.7-59.0), and 13.0 (1.6-106.8; P(trend) < 0.05) in CLUE I. Similar patterns were seen for congeners 138 and 153 and for total PCBs. Limited evidence of exposure-response trends was also observed for several other congeners. The primary 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane metabolite, p,p'-DDE, was not significantly associated with NHL in most analyses but slightly to moderately confounded the PCB associations. The results from these three cohorts suggest that concentrations of certain PCBs in blood are associated with increased risk of NHL.

Thyroid hormone status of Atlantic croaker exposed to Aroclor 1254 and selected PCB congeners

Atlantic croaker ( Micropogonias undulatus) were exposed to the polychlorinated biphenyl (PCB) mixture (Aroclor 1254) or one of three individual congeners (planar PCB 77 or ortho-substituted PCB 47 and PCB 153) in the diet for 30 days to investigate the effects of PCBs on circulating thyroid hormones, thyroxine (T 4) and triiodothyronine (T 3). Aroclor 1254 (0.2 and 1.0 mg/kg body mass/day) decreased plasma T 3 levels consistently, but the effects on T 4 levels were inconsistent from year to year. Exposure to PCB 153 (0.1 and 1.0 mg/kg body mass/day) significantly lowered both T 4 and T 3, while PCB 47 at the same doses had no effect on thyroid hormone levels. The lower doses of PCB 77 (0.004, 0.01 and 0.02 mg/kg body mass/day) had no effect on T 4 or T 3, whereas the highest dose (0.1 mg/kg body mass/day) increased T 4 levels significantly. The results of the present study demonstrate that exposure to PCBs at environmentally realistic concentrations can have profound effects on the thyroid status of Atlantic croaker. The ortho-substituted PCB 153 appears to contribute at least partially to the deleterious effects of Aroclor 1254 on thyroid status, whereas the planar PCB 77 at concentrations present in the mixture is unlikely to alter thyroid hormone levels.

Persistent organic pollutants in European background air: derivation of temporal and latitudinal trends

Data are presented for polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), polybrominated diphenyls ethers (PBDEs) and selected organochlorine compounds (OCs) in passive air samplers (PAS) along a rural/remote latitudinal transect from southern UK to northern Norway during 2002-2004. This study is part of an ongoing campaign, using semi-permeable membrane devices (SPMDs) as PAS over two year intervals since 1994. Data for PCBs, selected OCs and PBDEs are compared with that from previous campaigns. Absolute sequestered amounts of selected PCB congeners have decreased in a first order fashion between 1994-2004, with an average atmospheric clearance rate of 4.1 +/- 0.6 years and continue to fractionate with latitude. HCB has also declined between 1998-2004, with a clearance rate of 6 +/- 2.4 years. Data on DDT and its breakdown products indicate little fresh release in Europe. Comparison of PBDEs in 2000-02 and 2002-04 indicates site differences, generally with increases at UK sites and decreases in Norway. BDE-28, 47 and 49 decreased with increasing latitude (p < 0.04), while the other congeners did not show any significant latitudinal dependence. Transect data are presented for PAHs the first time. Three- and 4-ringed compounds dominated the mixture present in the SPMD. The PAH composition of the SPMDs at site 3 was compared to the average composition taken by active sampling at the same site. SPMD performance for sampling PAHs leaves many uncertainties, but they can be successfully used to semiquantitatively detect PAHs in the atmosphere. Fluorene and phenanthrene increased with latitude (p > 0.05), while 1-methylphenanthere, fluoranthene, benzo[b]fluoranthene and indeno[123-cd]pyrene decreased. Results are discussed in terms of sources, long-range atmospheric transport, global fractionation and clearance processes.

Bioaccumulation of PCBs in Burbot (Lota lota L.) After Delivery in Natural Food

Burbot (Lota lota) caught from Lake Päijänne, Central Finland, were exposed under laboratory conditions to four polychlorinated biphenyl (PCB) congeners delivered through diet, and accumulation of congeners to muscle, intestine, gonads, and liver were determined. The selected PCB congeners (PCB18, PCB44, PCB137, and PCB169) were added to intact dead vendace (Coregonus albula) and burbot were fed 5 or 10 contaminated meals (2- and 4-week experiment, respectively). Concentrations of fed congeners were different in the examined tissues. The highest concentrations of all the congeners were found in the livers of burbot. The mean retention efficiencies were 65.0% and 81.7% after 5 and 10 oral doses, respectively. The retention efficiency of the coplanar 169 was lower than those of the other fed congeners. The background organochlorine concentrations of the burbot of this study were compared with the PCB concentrations of burbot caught in the 1970s from Lake Päijänne. These concentrations were compared in order to clarify the PCB load and persistence in a boreal aquatic food web. The total PCB concentration in burbot has not declined during the last decades. The most abundant PCB congeners in the field were PCB138 and PCB153. Residual concentrations of pesticides were also found, especially the DDE, which is a metabolite of DDT.

Apoptosis-mediated neurotoxic potential of a planar (PCB 77) and a nonplanar (PCB 153) polychlorinated biphenyl congeners in neuronal cell cultures

Polychlorinated biphenyls (PCBs) are ubiquitous environmental contaminants, some of which may be neurotoxic depending on the chemical structure of the congeners. This study investigated the neurotoxic potential of 3,3′,4,4′-tetrachlorobiphenyl (TCB) (PCB 77, a non- ortho-substituted planar congener) and 2,2′,4,4′,5,5′-hexachlorobiphenyl (HCB) (PCB 153, a di- ortho-substituted nonplanar congener) by assessing cell viability and apoptotic cell death in neuronal cell cultures. We have combined morphological and biochemical techniques to establish the relevance of apoptosis in neuronal cell death induced by the two selected PCB congeners. Treatment with both planar and nonplanar congeners caused the loss of cell viability and accelerated apoptosis in a time- and concentration-dependent manner. However, the extent of apoptosis generated was greater for the non- ortho-substituted planar congener (PCB 77) than for the di- ortho-substituted nonplanar congener (PCB 153). This was correlated with the loss of cell viability since the planar congener was more cytotoxic. Based on our findings, the apoptosis induced by PCBs involves the increase of caspase-3 activity in neuronal cell cultures. It is reasonable to assume that PCB-induced apoptosis may be linked to the neurotoxic effect of these toxicants and that different molecular mechanisms may operate in the induction of apoptosis depending on the planarity or nonplanarity of the PCB congeners.