Total PCB Concentrations Research Articles

Bioanalytical and non-targeted mass spectrometric screening for contaminants of emerging concern in Southern California bight sediments

Assessing the impact of chemical contaminants on aquatic ecosystem health remains challenging due to complex exposure scenarios and the myriad of impact metrics to consider. To expand the breadth of compounds monitored and evaluate the potential hazard of environmental mixtures, cell-based bioassays (estrogen receptor alpha (ERα) and aryl hydrocarbon receptor (AhR)) and non-targeted chemical analyses with high resolution mass spectrometry (NTA-HRMS) were used to assess the quality of ∼70 marine sediment samples collected from 5 distinct coastal and offshore habitats of the Southern California Bight. AhR responses (<0.12–4.5 ng TCDD/g dry weight) were more frequently detectable and more variable than for ERα (<0.1–0.5 ng E2/g dry weight). The range of AhR and ERα responses increased by habitat as follows: Channel Islands < Mid-shelf < Marinas < Ports < Estuaries. The narrow range and magnitude of ERα screening response suggested limited potential for estrogenic impacts across sediments from all 5 habitats. The AhR response was positively correlated with total PAH and PCB concentrations and corresponded with a chemical score index representing the severity of metal and organic contamination. NTA-HRMS fingerprints generated in positive electrospray ionization mode were clearly distinguishable among coastal vs. offshore samples, with the greatest chemical complexity (n = 982 features detected) observed in estuarine sediment from a highly urbanized watershed (Los Angeles River). The concordance and complementary nature of bioscreening and NTA-HRMS results indicates their utility as holistic proxies for sediment quality, and when analyzed in conjunction with routine targeted chemical monitoring, show promise in identifying unexpected contaminants and novel toxicants.

Characterization, source and risk assessments of sediment contaminants (PCDD/Fs, DL-PCBs, PAHs, PCBs, OCPs, metals) in the urban water supply area

Water resources are becoming more valuable day by day. They need to evaluate the pollution and risk situations of the sources that supply water in detail. It is aimed to determine the level of POPs (PCDD/Fs, DL-PCBs, PAHs, PCBs, and OCPs) and metals, which are persistent pollutants, in the surface sediments taken from Yuvacık lake to reveal their possible sources, and to make toxicological and ecological risk assessments of sediment quality. It is one of the most comprehensive studies on the sediment scale for a drinking water source and is a first for the study area. Seventeen 2,3,7,8-substituted PCDD/Fs were analyzed with US EPA method (M.1613). The concentrations of all POPs were determined by GC-MS/MS. The range of ∑PCDD/F is 3.171 (Y8) to 28.42 (Y10) pg/g, with the highest concentrations of OCDD and 1234678-HpCDF compounds. Total DL-PCB concentrations 6.369 (Y8) to 37.41 (Y9) pg/g Total PAH concentrations in the samples ranged from 36.97 ng/g (Y1) to 81.38 ng/g (Y10). The PAH compounds with the highest concentrations at all sampled points were Phenanthrene 3141 (Y7) - 21,636 (Y10) and Naphthalene (11.40–19.41) ng/g. Total OCP concentrations ranged from 1.045 ng/g (Y8) to 4.179 ng/g (Y2), while total PCB concentrations ranged from 0.308 (Y1) to 1.55029 (Y9) ng/g. DDT p,p (0.4078–3.2544 ng/g) has the highest concentration among OCPs. PCB 101, 153, 138, and 180 are the highest detected PCB congeners. As a result of the source analysis, three different main sources were determined for all pollutant groups. They show accumulation in the sediment as a result of long-distance atmospheric transport. Toxicological values were found below acceptable limits. The main metals posing ecological risk were Ag, Cu, and Cd. Monitoring of POPs and assessing their toxicological and ecological risks are important for planning water resources and should be applied especially for critical basins.

Application of a pharmacokinetic model in characterizing sources of polychlorinated biphenyl exposure and determining threshold daily intakes for adverse health effects in infants and toddlers

Characterization of PCB exposure sources for vulnerable population groups is essential to minimize the health effects of PCB exposure. At the same time, it is important to consolidate the knowledge on threshold intakes of PCBs for infants and toddlers to prevent health effects. We estimated total PCB concentrations from birth to 2 years of age in children from Slovak and Czech populations, which continue to have high PCB concentrations in breast milk. Using a pharmacokinetic (PK) model, we characterized dominant PCB exposure sources and estimated new threshold estimated daily intakes (TEDI) (above which adverse effects cannot be excluded) for postnatal PCB exposure in infants and toddlers. In the PK model, concentrations of seven indicator PCBs in breast milk and cord blood samples from 291 mother-child pairs from the Slovak birth cohort, and 396 breast milk samples from Czech mothers we used, together with their physiological characteristics and PCB concentrations from other exposure sources (food, dust, air). The estimated total PCB concentrations in children's blood at different ages were compared with threshold PCB concentrations of 500, 700 and 1000 ng·glipid−1 in serum proposed by the French Agency for Food, Environmental and Occupational Health & Safety (ANSES) and the German Environment Agency (UBA), above which possible adverse health effects may be expected. We estimated that up to 20.6% of Slovak children and up to 45.7% of Czech children at two years of age exceeded the threshold value of 700 ng·glipid−1 in blood. Mean TEDIs leading to values of 500 ng·glipid−1 in blood for children up to two years ranged between 110 and 220 ng·kg−1·bw·day−1, varying according to breastfeeding duration. Breast milk and prenatal exposure contributed to 71%–85% of PCBs exposure at two years of age. In contrast, the contributions of PCBs from dust and indoor air were negligible.

Damselfish Embryos as a Bioindicator for Military Contamination on Coral Reefs at Johnston Atoll, Pacific Ocean

This study investigated the association between sediment contamination, PCB accumulation in adult nesting males and the occurrence of embryonic abnormalities in the damselfish, Abudefduf sordidus, from two sites with high PCB contamination and three “reference” sites (contaminants very low or not measurable) within Johnston Atoll, Central Pacific Ocean. Developmental abnormalities were assessed in damselfish embryos collected in the field during four natural spawning seasons (1996, 1998, 1999, and 2001). Laboratory incubations of abnormal embryos demonstrated that the observed abnormalities were lethal. PCBs were measured in fish collected in three years. Mean whole-body concentrations of total PCBs ranged from 364.6 to 138,032.5 ng/g lipid. A significant residue–effect relationship was found between total PCB concentration and embryo abnormalities. The occurrence of embryo abnormalities was positively related to fish PCB concentration (other contaminants were also evaluated including metals and dioxins). This study demonstrates the utility of using damselfish embryos as a bioindicator tool for monitoring coral reefs. It also provides baseline-monitoring criteria and evaluates sediment quality benchmarks used for ecological risk assessments on coral reefs.

Spatial distribution, source identification and ecological risk assessment of POPs and heavy metals in lake sediments of Istanbul, Turkey

Istanbul needs to be protected and constantly monitored water resources due to its increasing population and the decrease in precipitation. This study aims to comprehensively reveal surface sediments collected from reservoirs that supply water to Istanbul concerning POPs (PAHs, PCBs, and OCPs) and heavy metals; to identify possible sources of PAHs, and conduct their ecological risk assessment. Pollution indices in this study were used as contamination degree (CD) contamination factor (CF), geoaccumulation index (Igeo), pollution load index (PLI) and Sediment Quality Guidelines (SQGs). Total PAH concentrations of surface sediments at the sampling points ranged from 46.29 ng/g (A7) to 403.9 ng/g (A15). Benzo(b)fluoranthene (5.647–59.42 ng/g), Pyrene (3.625–83.10 ng/g), Fluoranthene (3.363–66.48 ng/g), Phenanthrene (3.115–52.48 ng/g), Chrysene (3.532–43.98 ng/g), Naphthalene (6.606–36.20 ng/g), Benzo(g,h,i)perylene (3.316–41.73 ng/g) and Indeno(1,2,3-c,d)pyrene (3.453–38.84 ng/g) are the dominant PAH compounds. PAH pollution may be caused by the village-town settlements near the dam and the O7-D020 highway. Total OCP concentration ranged from 2.233 ng/g (A12) to 7.337 ng/g (A1), while total PCB concentration ranged from 0.246 ng/g (A13) to 3.708 ng/g (A1). The lowest total OCP and PCB concentrations were found in surface sediments taken from Kazandere, Papuçdere and Alibey Dam lakes. DDT p,p (0.072–5.177 ng/g) has the highest concentration among all sediment samples. While the most dominant OCP compounds in the samples were DDT p,p, DDE p,p and DDD p,p, HCH alpha, HCH beta, respectively, PCB 153, 138 and 180 were the highest detected PCB congeners in the same samples. Total heavy metal concentration varied from 77,812 mg/kg to 267,072 mg/kg. According to PAH diagnostic analysis, the surface sediments of Terkos, Büyükçekmece, Elmalı, Darlık, Sazlıdere, Alibey and Ömerli Dams were polluted by petrogenic sources, while the surface sediments of Kazandere and Papuçdere Dams were affected by pyrogenic sources. None of the levels of POPs in the samples exceeded the ERM values. Slight and moderate contamination of heavy metals, such as Pb and Zn, were present in most of the sampling points according to CD, CF, PLI and Igeo values. The quality criteria of heavy metals showed that almost all of the sampling points had Cd, Pb and Hg concentrations below the ERL values. The Ni concentrations at most of the sampling points significantly exceeded the ERM values. The concentrations of As, Cr, Cu and especially Ni and Zn exhibit a significant toxic risk to aquatic organisms to sediment quality criteria.

Passive Air Sampling of PCDD/Fs, PCBs, PAEs, DEHA, and PAHs from Informal Electronic Waste Recycling and Allied Sectors in Indian Megacities.

Xenobiotic chemical emissions from the informal electronic waste recycling (EW) sector are emerging problem for developing countries, with scale and impacts that are yet to be evaluated. We report an intensive polyurethane foam disk passive air sampling study in four megacities in India to investigate atmospheric organic pollutants along five transects viz., EW, information technology (IT), industrial, residential, and dumpsites. Intraurban emission sources were estimated and attributed by trajectory modeling and positive matrix factorization (PMF). ∑17PCDD/Fs, ∑25PCBs, ∑7plasticizers, and ∑15PAHs concentrations ranged from 3.1 to 26 pg/m3 (14 ± 7; Avg ± SD), 0.5-52 ng/m3 (9 ± 12); 7.5-520 ng/m3, (63 ± 107) and 6-33 ng/m3 (17 ± 6), respectively. EW contributed 45% of total PCB concentrations in this study and was evidenced as a major factor by PMF. The dominance of dioxin-like PCBs (dl-PCBs), particularly PCB-126, reflects combustion as the possible primary emission source. PCDD/Fs, PCBs and plasticizers were consistently highest at EW transect, while PAHs were maximum in industrial transect followed by EW. Concentrations of marker plasticizers (DnBP and DEHP) released during EW activities were significantly higher (p < 0.05) in Bangalore than in other cities. Toxic equivalents (TEQs) due to dl-PCBs was maximum in the EW transect and PCB-126 was the major contributor. For both youth and adult, the highest estimated inhalation risks for dl-PCBs and plasticizers were seen at the EW transect in Bangalore, followed by Chennai and New Delhi.

Occurrence of polychlorinated biphenyl congeners in marine sediment of Makran region, Chabahr bay, Iran

In this study, selected PCB congeners (IUPAC numbers 28, 52, 101, 138, 153, and 180) were quantified in 34 stations of Chabahr bay and around it in the Makran region of Iran. The sum of total PCB concentrations varied from below the detection limit to 485 ng kg−1 dry weight of sediment. Based on the Canadian Sediment Quality Guidelines, the effect of detected PCBs was negligible for aquatic organisms. According to the dominance of PCB 28 and 52 with average range of 62 to 100% of total PCBs, maritime transportation and atmospheric deposition appear to be the important source of PCBs in this region. Further, the presence of components of commercial products such as ClophenA50 appears to be one of the probable sources.

Polychlorinated biphenyls in indoor dust from urban dwellings of Lahore, Pakistan: Congener profile, toxicity equivalency, and human health implications.

This study is the pioneer assessment of the PCBs in indoor dust particles (from air conditioners) of an urbanized megacity from South Asian. The ∑35 PCB concentration ranged from 0.27 to 152.9ng/g (mean: 24.84±22.10ng/g). The tri- and tetra-PCBs were dominant homologues, contributing 57.36% of the total PCB concentrations. The mean levels of Σ8 -dioxin-like (DL), Σ6 -indicator PCBs and WHO2005 -TEQ for DL-PCBs were 2.22±2.55ng/g, 9.49±8.04ng/g and 4.77±4.89pg/g, respectively. The multiple linear regression indicated a significant correlation of dusting frequency (p=1.06×10-04) and age of the house (p=1.02×10-06) with PCB concentrations in indoor environment. The spatial variation of PCB profile revealed relatively higher concentrations from sites near to illegal waste burning spots, electrical locomotive workshops, and grid stations. Human health risk assessment of PCBs for adults and toddlers through all three exposure routes (ie, inhalation, ingestion, and dermal contact) demonstrated that toddlers were vulnerable to high cancer risk (4.32×10-04 ), while adults were susceptible from low to moderate levels of risk (3.16×10-05 ). Therefore, comprehensive investigations for PCBs in the indoor settings, focusing particularly on the sensitive populations with relationship to the electronic devices, transformers, and illegal waste burning sites, are recommended.

Distribution and ECo-Toxicological Risk Assessment of Legacy Persistent Organic Pollutants in Surface Water of Talar, Babolrood and Haraz Rivers

In the outer Alborz Range in the Northern Province of Iran, the Haraz, Talar and Babolrood Rivers are the three largest rivers where most of the agricultural, aquacultural and industrial activities are found. Total indicator polychlorinated biphenyls (iPCBs) ranged ND–474, ND–273 and ND–559 ng/L in Haraz, Talar and Babolrood Rivers, respectively. Significantly lower (p &lt; 0.05) concentrations of DDT, lindane and dieldrin were observed in the upstream stations than downstream stations of both Babolrood and Haraz Rivers. However, in Talar River, PCB residues in upstream was significantly higher (p &lt; 0.05) than downstream. Furthermore, PCB-28 in Talar River and PCB-101 and PCB-153 in Bablrood and Haraz Rivers were high in water samples at all stations. A significant difference was observed among the stations. In October, November and December, there was negligible variations in total PCB concentration among the stations. Alarming levels of some of the legacy persistent organic pollutants (POPs) may pose adverse effects on the aquatic species dwelling in the Talar, Babolrood and Haraz Rivers of Iran.

Assessment of PCB contamination, the potential for in situ microbial dechlorination and natural attenuation in an urban watershed at the East Coast of the United States

Sediment contamination is a major environmental issue in many urban watersheds and coastal areas due to the potential toxic effects of contaminants on biota and human health. Characterizing and delineating areas of sediment contamination and toxicity are important goals of coastal resource management in terms of ecological and economical perspectives. Core and surficial sediment samples were collected from an industrialized urban watershed at the East Coast of the United Stated and analyzed to evaluate the PCB contamination profile and toxicity resulting from dioxin-like PCBs as well as reductive dechlorination potential of indigenous PCB halorespiring bacteria through dechlorination activity assays. To support the experimental results an anaerobic dechlorination model was applied to identify microbial dechlorination pathways. The total PCB concentration in core samples ranged from 3.9 to 225.6 ng/g·dry weight (dw) decreasing with depth compared to 353.2 to 1213.7 ng/g·dw in surficial samples. The results of this study indicated an increase in PCB contamination over the last century as the industrial activity intensified. The toxicity resulting from dioxin-like PCBs was reduced up to 94% in core samples via 21 pathways resulting from the dechlorination model. Dechlorination rates in surficial sediment were between 1.8 and 13.2 · 10−3 mol% PCB116/day, while lower rates occurred in the core sediment samples. Dechlorination was achieved mainly through meta followed by para dechlorination. However, the rarer ortho dechlorination was also observed. Detection of indigenous PCB dechlorinating bacteria in the sediments and reduction of toxicity indicated potential for natural attenuation when point and nonpoint source PCBs in the urban watershed are controlled and PCB loading reduced.

Organohalogen contaminants in common loons (Gavia immer) breeding in Western Alberta, Canada

We examined the influence of biological and geographical factors on the levels and patterns of organohalogen contaminants in blood of adult common loons (Gavia immer) collected from 20 lakes in Alberta, Canada. The loons were captured in the 2006 and 2007 breeding seasons over a 900 m elevation gradient across the eastern slope of the Canadian Rocky Mountains. While PCBs dominated the composition of these contaminants in loons at all sites (∑PCBs > p,p’-DDE > ∑PBDEs > ∑Chlordanes > HCB), p,p’-DDE and ∑PBDEs were also important, averaging approximately 50% and 20% of total PCB concentrations, respectively. ∑PCBs and ∑PBDEs were higher in males than in females. Inter-lake variation was apparent for contaminant concentrations and patterns and were largely explained by dietary signatures (δ15N and δ13C) and proximity to a large hydroelectric dam. Mean ∑PCB (19.6 ng/g wet weight (ww)) and organochlorine pesticide (OCP) (p,p’-DDE: 11.8 ng/g, cis-nonachlor: 0.10 ng/g, trans-nonachlor: 0.32 ng/g, HCB: 0.34 ng/g ww) concentrations in loons were approximately 4- to 17-fold lower than average concentrations reported in common loons from Atlantic Canada and were well below concentrations which have been associated with impaired reproductive success and eggshell thinning in other piscivorous birds. Dominant PBDE congeners were BDE47, BDE99, and BDE100. The regional mean for ∑PBDEs (4.04 ng/g ww) in loons from the present study was within the range reported for ∑PBDEs in nestling bald eagle plasma from British Columbia. This is the first report of PBDEs in loons and the first report of PCBs and OCPs in common loons from Western North America.

Aroclor misidentification in environmental samples: how do we communicate more effectively between the laboratory and the data user?

Disposal of carbonless copy paper (CCP) paper sludge during the 1960s contaminated a site in the USA with PCBs. Despite historic records of CCP sludge disposal and absence of evidence of any other disposal, a dispute arose among the parties over the source of the PCBs. Aroclor 1242 is well documented as the PCB mixture used in CCP, yet Aroclors 1242, 1248, 1254, and 1260 were reported by the analytical laboratory. How could the PCBs at a single, small site be reported as four different Aroclors? Some claimed that there had to be at least four Aroclors source inputs to the site. Disposal of four different Aroclors at this site would simply defy logic and the historic record. Weathering of the mixtures is part of the story. A larger issue is the conflict between the intent of the USEPA 8082 method to determine the total PCB content in environmental samples to facilitate environmental cleanup and disposal decisions within a regulatory context versus the data users' intent to identify the PCB sources. This inappropriate extension of the data leads to erroneous conclusions. To mitigate problems like this, laboratory analysis requests need to be matched to the intended data usage; conversely, the data must not be over-interpreted beyond the limits of the method. The PCB analysis community needs to develop a better articulation of the limits of Aroclor identification for the broader community that may naïvely assume that if the laboratory reports "Aroclor 1248," then someone must have placed Aroclor 1248 at the site. After all, when a laboratory reports "lead" or "chloroform," those identifications are never in question.

Influence of Selected Coagulants of Indicator and Dioxin-Like PCB Removal from Drinking Water

Abstract The aim of the research was to compare selected coagulants efficiency in indicator and chosen dioxin-like PCB removal from surface water. As coagulants, there were used aluminium sulfate and 5 hydrolyzed polyaluminium chlorides, with trade names: PAX-XL1, PAX-XL10, PAX-XL19, PAX-XL60, PAX-XL69. For the research, surface water was used, collected from dam reservoir. The water composition was modified with standard mixtures PCB MIX24 and MIX13, in order to obtain concentration of each congener equal to 300 ng/dm3. The PCB MIX24 mixture was composed of indicator congeners solution: 28, 52, 101, 118, 138, 153, and 180, whereas the MIX13 mixture - solution of three dioxin-like PCB 77, PCB 126, and PCB 169. It was demonstrated that the application of aluminium sulfate allowed for reaching better effects for purifying water of PCB, than with the usage of pre-hydrolyzed salts, polyaluminium chlorides. Out of the studied coagulants, the best effects for indicator PCB removal were obtained with the application of aluminium sulfate, total PCB concentration was decreased by 65%. The highest efficiency for indicator congeners removal (90%) was obtained for PCB 138 and 153. After the application of hydrolyzed polyaluminium chlorides PAX-XL1, PAX-XL10 decrease in higher chlorinated PCB concentration was obtained, in the range of 23 to 74%. Selectivity of chosen PCB congener removal, depending on applied coagulant, was demonstrated; with the usage of aluminium sulfate, removal of heptachlorobiphenyl PCB 180 at the level of 34% was obtained, whereas with the application of PAX-XL1 and PAX-XL10 higher reduction efficiency for this congener was obtained, i.e. 83 and 74% respectively. For dioxin-like PCB, after application of aluminium sulfate, total concentration reduction by 74% was obtained, efficiency of this congeners removal amounted to from 54 (PCB 77) up to 72% (PCB 126), similar results were obtained after the usage of PAX-XL1. The lowest PCB removal from water rate was stated for coagulants PAX-XL60 and PAX-XL69.

A modeling approach to compare ΣPCB concentrations between congener-specific analyses.

Changes in analytical methods over time pose problems for assessing long-term trends in environmental contamination by PCBs. Congener-specific analyses vary widely in the number and identity of the 209 distinct PCB chemical configurations (congeners) that are quantified, leading to inconsistencies among summed PCB concentrations (ΣPCB) reported by different studies. Here, we present a modeling approach using linear regression to compare ΣPCB concentrations derived from different congener-specific analyses measuring different co-eluting groups. The approach can be used to develop a specific conversion model between any 2 sets of congener-specific analytical data from similar samples (similar matrix and geographic origin). We demonstrate the method by developing a conversion model for an example data set that includes data from 2 different analytical methods, a low resolution method quantifying 119 congeners and a high resolution method quantifying all 209 congeners. We used the model to show that the 119-congener set captured most (93%) of the total PCB concentration (i.e., Σ209 PCB) in sediment and biological samples. ΣPCB concentrations estimated using the model closely matched measured values (mean relative percent difference = 9.6). General applications of the modeling approach include 1) generating comparable ΣPCB concentrations for samples that were analyzed for different congener sets; and 2) estimating the proportional contribution of different congener sets to ΣPCB. This approach may be especially valuable for enabling comparison of long-term remediation monitoring results even as analytical methods change over time. Integr Environ Assess Manag 2017;13:227-232. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.

Enhancement of coagulation process with powdered activated carbon in PCB and heavy metal ions removal from drinking water

Suitability of powdered activated carbon CWZ-30 for enhancing the coagulation process used for the removal of contaminants from surface water was evaluated. Aluminium sulphate, aluminium chloride and pre-hydrolysed polyaluminium chloride (PAX18 and PAX-XL1905) were used as coagulants, and the following parameters were analysed in water sampled from the Kozłowa Góra dam reservoir (Poland): concentrations of heavy metals (Cu, Cd, Ni, Pb) and indicator PCBs (28, 52, 101, 118, 138, 153, 180). The highest reduction in heavy metal concentration was obtained with the use of PAX-XL1905. It amounted, in case of copper, cadmium, nickel and lead, to 64, 39, 18 and 85%, respectively. Enhancement of coagulation with powdered activated carbon CWZ-30 in the amount of 30 mg L−1, increased the efficiency of these metals removal up to 79, 53, 26 and 95%, respectively. The best results for total PCB concentration removal were obtained with the use of PAX18. Application of powdered activated carbon also allowed to obtain better effects of PCB removal from water. Therefore, the coagulation process enhanced with powdered activated carbon had crucial impact on the reduction of analysed heavy metals concentration and indicator PCBs.

Compositional Variation of PCBs, PAHs, and OCPs at Gas Phase and Size Segregated Particle Phase during Dust Incursion from the Saharan Desert in the Northwestern Anatolian Peninsula

A dust incursion occurred in Istanbul on 1 February 2015 from the Saharan Desert. During this episode, 938 μg·m−3of TSP concentration was observed. TSP concentration was 64 μg·m−3and 78 μg·m−3on the following two days. Particles of 3 μm were dominant during the episode; however, particles &lt; 0.49 μm were dominant after the episode. The averages of total (gas + particle) PCB, PAH, and OCP concentrations were 279 pg·m−3, 175 ng·m−3, and 589 pg·m−3, respectively. Tri-CBs were dominant in most of the samples. Flt and Phe had the highest contribution to PAH species.β-HCH and heptachlor had the highest share in terms of OCPs. Particle phase PCBs exhibited monomodal size distribution, whereas OCPs had bimodal size distribution. PAHs exhibited either monomodal or bimodal size distribution on different days. The mass median diameter of PAHs did not change significantly during different atmospheric conditions due to their local sources. Gas/particle partitioning of each pollutant was evaluated by plotting their subcooled vapor pressure against the partitioning coefficient. From 1 to 3 February, the slope of the regression line shifted close to −1, indicating that the least favorable conditions were present during dust incursion for an equilibrium state.

A novel pollution pattern: Highly chlorinated biphenyls retained in Black-crowned night heron (Nycticorax nycticorax) and Whiskered tern (Chlidonias hybrida) from the Yangtze River Delta

Contamination of organochlorine pesticides (OCPs), polychlorinated diphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), hydroxylated polybrominated diphenyl ethers (OH-PBDEs) and their methylated counterparts (MeO-PBDEs) were determined in Black-crowned night heron (Nycticorax nycticorax) and Whiskered tern (Chlidonias hybrida) from two drinking water sources, e.g. Tianmu lake and East Tai lake in Yangtze River Delta, China. A novel PCBs contamination pattern was detected, including 11% and 6.9% highly chlorinated biphenyls (PCBs with eight to ten chlorines) in relation to total PCB concentrations in the Black-crowned night heron and Whiskered tern eggs, respectively. The predominating OCPs detected in the present study were 4,4′-DDE, with concentration range 280–650 ng g−1 lw in Black-crowned night heron and 240–480 ng g−1 lw in Whiskered tern, followed by β-HCH and Mirex. 6-MeO-BDE-90 and 6-MeO-BDE-99 are the two predominant congeners of MeO-PBDEs whereas 6-OH-BDE-47 contributes mostly to the OH-PBDEs in both species. Contamination level was considered as median or low level compared global data.

Nano-occurrence and removal of PCBs within the Europe's largest petrochemical MBR system

The occurrence of 45 PCBs was studied in a wastewater treatment plant (WWTP), which treats industrial wastewater from the zone of Porto Marghera (Venice, Italy) in an MBR, and in the Naviglio del Brenta River, which serves as a source of process water supply for this industrial zone. The focus of the study was placed on the comparison of levels of contamination of the WWTP effluent and the river water by selected PCBs in order to understand the major source of PCB pollution for the Lagoon of Venice and contrast them with the current legislation. Out of 45, 31 PCBs were detected in the WWTP at total median PCB concentration of 5.5 ng/L with a predominant presence of six indicator – PCBs (PCB 28, 52, 101, 138, 153 and 180), which accounted for 50–55% of total PCBs in both wastewater and sludge samples. The total PCB concentration was reduced by around 90% during the applied wastewater treatment to a median concentration of 0.5 ng/L at the WWTP effluent. In the samples collected from the river, 27 PCBs were detected at total median concentration of 2.1 ng/L, which is few times higher than the total PCB concentration found in the WWTP effluent. This result suggests that the current legislative limitations applied to the WWTPs effluent discharges into the Lagoon of Venice, regarding the presence of PCBs (i.e. absent) is rather arbitrary given the higher concentration levels encountered in river water than in the WWTP effluent of the studied industrial WWTP.

Decadal re-evaluation of contaminant exposure and productivity of ospreys (Pandion haliaetus) nesting in Chesapeake Bay Regions of Concern

The last large-scale ecotoxicological study of ospreys (Pandion haliaetus) in Chesapeake Bay was conducted in 2000–2001 and focused on U.S. EPA-designated Regions of Concern (ROCs; Baltimore Harbor/Patapsco, Anacostia/middle Potomac, and Elizabeth Rivers). In 2011–2012, ROCs were re-evaluated to determine spatial and temporal trends in productivity and contaminants. Concentrations of p,p′-DDE were low in eggs and below the threshold associated with eggshell thinning. Eggs from the Anacostia/middle Potomac Rivers had lower total PCB concentrations in 2011 than in 2000; however, concentrations remained unchanged in Baltimore Harbor. Polybrominated diphenyl ether flame retardants declined by 40%, and five alternative brominated flame retardants were detected at low levels. Osprey productivity was adequate to sustain local populations, and there was no relation between productivity and halogenated contaminants. Our findings document continued recovery of the osprey population, declining levels of many persistent halogenated compounds, and modest evidence of genetic damage in nestlings from industrialized regions.

Human Serum from Urban and Rural Adolescents and Their Mothers Shows Exposure to Polychlorinated Biphenyls Not Found in Commercial Mixtures.

Although polychlorinated biphenyls are no longer sold as commercial mixtures, they are still being produced through modern manufacturing processes. We have previously shown that non-Aroclor PCB 11 is prevalent in indoor and outdoor air and sediment and detected in human serum. Here we report the prevalence of non-Aroclor PCB congeners (≤0.20 wt % in Aroclor) in human serum collected from urban and rural adolescents and their mothers. We hypothesized that additional non-Aroclor congeners are present in serum. Sera were extracted and detected for 209 PCBs using gas chromatography-tandem mass spectrometry. A list of 70 non-Aroclor PCB congeners was determined by measurement of original Aroclors. PCB 11, 14, 35, and 209 are the major dominating and most frequently detected congeners. PCB 14 and 35 have not been previously reported for environmental matrices. Adolescents have significantly lower total non-Aroclor PCB concentrations than mothers in East Chicago (p < 0.001) and Columbus Junction (p = 0.008). There are significant differences in non-Aroclor PCBs between East Chicago community and Columbus Junction community (p < 0.001). Non-Aroclor PCBs represent an average of 10% (and up to 50%) of total PCBs measured in serum. An average of 50% (and up to 100%) of these concentrations may be attributed to aryl azo and phthalocyanine paint pigments.