Spatial distribution and historical deposition behaviors of perfluoroalkyl substances (PFASs) in sediments of Lake Chaohu,a shallow eutrophic lake in Eastern China

Sediment samples were collected from the Chaohu Lake basin to investigate the spatial distribution and historical deposition behaviors of 17 perfluoroalkyl substances (PFASs). Concentrations of the total PFASs (∑PFASs) in limnetic sediments ranged from 0.719 to 2.429 ng/g dry weight (dw), with an average of 1.449 ng/g dw. A clear gradient in the spatial distribution was observed from west to east in surface sediments of Lake Chaohu. Perfluorooctane sulfonic acid and perfluorooctanoic acid were predominant in limnetic sediments, with an average of 0.383 and 0.275 ng/g dw, respectively. The ∑PFASs concentrations in riverine sediments were the highest in the Shiwuli River, followed by the Nanfei River. PFASs in riverine sediments indicated that industrial discharge and urban runoff played key roles in PFAS distribution and pollution levels. In vertical profiles, concentrations of the ∑PFASs and PFAS congeners in three sediment cores generally increased with decreasing depths, indicating that the input history of the ∑PFASs could be attributed to the development of industrialization and urbanization in the Chaohu Lake basin. The correlations between PFASs and sedimentary characteristics, organic carbon, nutrients and inorganic salts suggested that both hydrophobic and electrostatic effects played important roles in PFAS distribution and pollution levels in sediments of Lake Chaohu.     

Variation and distribution of total mercury in water, sediment and soil from northern Lake Victoria, East Africa

Lake Victoria, the world's largest tropical freshwater lake, is an important resource, ecologically and economically. THg distribution in the northern parts of the lake are not well known, so to answer this gap, patterns in total mercury (THg) in water, soil and two dated sediment cores from northern Lake Victoria were determined. Water THg concentrations ranged from 0.7 to 5.8 ng/L, and there were no apparent differences observed between Napoleon and Winam Gulfs. Two precipitation samples had Hg concentrations of 7 and 31 ng/L. Surface soil samples collected from various agricultural sites around Jinja, Napoleon Gulf, have THg concentrations between 12.7 and 48.4 ng/g dry weight; they were correlated with organic carbon, total phosphorus and % clay. A near-shore core taken in Itome Bay in Napoleon Gulf, and an offshore core collected from the deepest part of the lake had similar THg concentrations and profiles (78 to 458 ng/g dry weight). The increase in THg concentration in the profiles of both cores began around 1960 and peaked around 1980. The similar sedimentary THg profiles and fluxes in the cores suggest that the THg sources to L. Victoria are primarily atmospheric, with some erosion inputs, and that equatorial African ecosystems are not exempt from the global increase in baseline THg concentrations.     

Effects of co-exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin and perfluorooctane sulfonate or perfluorooctanoic acid on expression of cytochrome P450 isoforms in chicken (Gallus gallus) embryo hepatocyte cultures

In this study we investigated the effect of a single-compound exposure or two compound co-exposure to tetrachlorodibenzo-p-dioxin (TCDD) plus perfluorooctane sulfonate (PFOS) or perfluorooctanoic acid (PFOA) on the mRNA expression of cytochromes P450 (CYP) 1A4, 4V2 and 3A37, ethoxyresorufin-O-deethylase (EROD) activity and cell viability in chicken (Gallus gallus domesticus) embryo primary hepatocyte cultures. Cell viability after 24 h of incubation was significantly decreased in cells exposed to PFOS at concentrations between 30 µM and 60 µM with or without co-exposure to TCDD (0.3 nM at maximum). PFOA did not decrease cell viability even at maximum concentrations of 60 µM. TCDD induced CYP1A4 mRNA and EROD activity substantially as reported previously. PFOS also increased CYP1A4 mRNA in a concentration-dependent manner. Co-exposure of cells to PFOS plus TCDD did not change CYP1A4 mRNA levels compared to cells treated with TCDD alone. PFOS alone did not induce CYP4V2 mRNA, however 40–50 µM PFOS plus TCDD (0.3 nM) induced CYP4V2 mRNA compared to TCDD alone (P < 0.05). This trend was similar to that observed with co-exposure to TCDD plus PFOA, suggesting that PFOA alone did not induce CYP4V2 mRNA, whereas co-exposure to TCDD plus PFOA induced the expression levels. PFOS alone decreased CYP3A37 mRNA by a maximum of 45%, however after co-exposure to TCDD, recovery of mRNA expression to levels measured in DMSO-treated cells was observed. Our data suggest a complex gene response to mixtures of dioxin-like and perfluorinated compounds.     

Quantification of fluorotelomer-based chemicals in mammalian matrices by monitoring perfluoroalkyl chain fragments with GC/MS

Perfluorocarboxylic acids (PFCAs), namely perfluorooctanoic acid (PFOA) and perfluorononanoic acid (PFNA), have been identified as persistent, bioaccumulative and potentially toxic compounds. The structural analog, 8-2 fluorotelomer alcohol (8-2 fTOH) is considered the probable precursor of these stable metabolites. Because simultaneous quantification is needed for volatile and non-volatile perfluorinated chemicals (PFCs) in complex matrices, a GC/MS method was developed and tested based on selected ion monitoring of perfluorinated alkyl parent chain fragment ions. Although the method requires a derivatization step, combined GC/MS analysis of PFCA-me's and FTOHs increases analytical efficiency and decreases sample analysis time. The method instrument detection limits are between 7.1 and 24.5 ng/mL extract (MTBE), and the method quantification limits are below 50 ng/mL serum or ng/g liver for all PFCs investigated. Recoveries from mouse serum and liver homogenates, which were spiked with FTOHs and PFCAs at levels of 25 and 200 ng/mL or ng/g, ranged from 81 to 101%. Finally, the utility of the method was demonstrated by dosing male CD-1 mice with 30 mg/kg-BW of 8-2 fTOH and quantifying PFCs 6h post-treatment. The advantages of this method are (1) the simultaneous detection of both volatile and non-volatile fluorotelomer-based chemicals in complex matrices, such as mammalian tissues, (2) as a confirmatory method to LC-MS/MS, and (3) as an alternative method of analysis for laboratories without access to LC-MS/MS.     

Occurrence and distribution of organochlorine pesticide residue levels in water,sediment and aquatic weeds in the Nyando River catchment,Lake Victoria,Kenya

Samples of water, sediments and aquatic weeds were collected from 26 sites in the Nyando River catchment of the Lake Victoria basin in 2005–2006. The objective was to investigate levels of organochlorine pesticides that have either been banned or are restricted for use in Kenya. The pesticides investigated were lindane, aldrin, endosulfan, endrin, dieldrin, DDT, heptachlor and methoxychlor. These pesticides had previously found wide applications in public health and agriculture in Kenya for control of disease vectors and crop pests respectively. Results showed that mean concentrations were highest for methoxychlor (8.817 ± 0.020?µg l^?1) in water, sediments (92.893 ± 3.039 µg kg^?1), and weeds (39.641 ± 3.045?µg kg^?1), the weeds also tended to accumulate aldrin (15.519 ± 3.756?µg kg^?1). The results show that the pesticides are still in use and are detected in the catchment. Stringent management and public awareness measures are required to enforce the ban on the organochlorine pesticides in order to safeguard the environment and ecosystems of Lake Victoria.     

The inhibition of human and rat 11β-hydroxysteroid dehydrogenase 2 by perfluoroalkylated substances

11β-Hydroxysteroid dehydrogenase 2 (11β-HSD2) regulates active glucocorticoid access to glucocorticoid and mineralocorticoid receptors by metabolizing it to an inactive form. Perfluoroalkylated substances (PFASs) are man-made polyfluorinated compounds that are widely used and persistent in the environment. We tested the inhibitory potencies of four PFASs including perfluorooctanoic acid (PFOA), perfluorooctane sulfonate (PFOS), perfluorohexanesulfonate (PFHxS) and perfluorobutane sulfonate (PFBS) on human and rat 11β-HSD2. PFOS was a potent inhibitor of both human (IC(50)=48 nM) and rat (IC(50)=293 nM) 11β-HSD2 activities. The potencies for the inhibition of human and rat 11β-HSD2 activities were PFOS>PFOA>PFHxS>PFBS. PFASs showed competitive inhibition of both human and rat 11β-HSD2 activities. This observation indicates that PFOS is a potent endocrine disruptor for glucocorticoid metabolism. Article from the Special issue on Targeted Inhibitors.     

An in-vitro investigation of the effect of perfluorooctane sulphonate on cell lines of embryonic origin

Fluorinated organic compounds, such as perfluorooctane sulfonate, are stable chemicals with a wide range of industrial applications. The potential toxicity of perfluorooctane sulfonate is not well characterized, and even less known are the mechanisms underlying its toxic effects. Perfluorooctane sulfonate change of inner mitochondrial membrane permeability has been implicated as a potential mechanism of toxicity. In this study, we research that perfluorooctane sulfonate effects the expression of Apaf1 and Caspase3 genes in the amnion and fetal lung cell line that initiate the cells to undergo apoptosis. The expression of Caspase3 and Apaf1 was determined by using quantitative RT-PCR. In the study there is significant increase in expression of Caspase3 and Apaf1 in amnion and fetal lung cell line exposed to high dose (p < 0.001, p = 0.004). Also there is significant increase in cell lines exposed for a long period of time to perfluorooctane sulfonate (p = 0.001). But no significant increase was seen in the low doses and exposed for a short period of time. In conclusion, apoptotic gene expression is increase in cells exposed perfluorooctane sulfonate by dose dependent manner was determined. So this work is the first study examines the apoptotic effects of perfluorooctane sulfonate in human embryonic cells it will lead the way to the other topical studies.     

Surficial sediment phosphorus fractions along a biogeochemical gradient in Nyanza (Winam) Gulf, northeastern Lake Victoria and their possible role in phosphorus recycling and internal loading

Different phosphorus fractions and metal element composition of surficial sediments were measured on three occasions in 2005 and 2006 along a transect between Nyanza Gulf and offshore Lake Victoria, in order to assess the potential for sediments to contribute to the water column P concentrations in Lake Victoria. Total phosphorus (TP), apatite phosphorus (AP), inorganic phosphorus (IP) and organic phosphorus (OP) increased in sediments along the gulf towards the main lake while the non-apatite inorganic phosphorus (NAIP) increases were less defined. The longitudinal gradient of sediment TP and its fractions in Nyanza Gulf is a result of high rates of terrigenous input and resuspension and transport of the light, phosphorus rich inorganic and organic matter towards the main lake. TP in the sediment ranged from 812.7 to 1,738 mg/kg dry weight (DW) and was highest in the Rusinga Channel, the exchange zone between the gulf and the main lake. AP was the most important TP fraction, contributing between 35 and 57.3% of TP. Ca content in the sediment was strongly associated with TP and AP in the sediment (r² = 0.92 and 0.98, respectively) in the gulf and the channel, indicating the importance of apatite in controlling P availability in these zones. In the gulf and the Rusinga Channel, the less bioavailable apatite phosphorus dominated, whereas in the deeper main lake OP was the major fraction illustrating the importance of anaerobic release of P from sediments and acceleration of internal P loading in the main lake.     

Specific method for determination of gefitinib in human plasma, mouse plasma and tissues using high performance liquid chromatography coupled to tandem mass spectrometry

A rapid, sensitive and specific method was developed and validated using liquid chromatography-tandem mass spectrometry (LC/MS/MS) for determination of gefitinib in human plasma and mouse plasma and tissue. Sample preparation involved a single protein precipitation step by the addition of 0.1 mL of plasma or a 200 mg/mL tissue homogenate diluted 1/10 in human plasma with 0.3 mL acetonitrile. Separation of the compounds of interest, including the internal standard (d8)-gefitinib, was achieved on a Waters X-Terra C18 (50 mm x 2.1 mm i.d., 3.5 microm) analytical column using a mobile phase consisting of acetonitrile-water (70:30, v/v) containing 0.1% formic acid and isocratic flow at 0.15 mL/min for 3 min. The analytes were monitored by tandem mass spectrometry with electrospray positive ionization. Linear calibration curves were generated over the range of 1-1000 ng/mL for the human plasma samples and 5-1000 ng/mL for mouse plasma and tissue samples with values for the coefficient of determination of > 0.99. The values for both within- and between-day precision and accuracy were well within the generally accepted criteria for analytical methods (< 15%). This method was subsequently used to measure concentrations of gefitinib in mice following administration of a single dose of 150 mg/kg intraperitoneally and in cancer patients receiving an oral daily dose of 250 mg.     

Organochlorine Pesticides in Sediments around Chaohu Lake: Concentration Levels and Vertical Distribution

Eighteen organochlorine pesticides (OCPs) were investigated in surface sediments from the Nanfei River and in four sediment cores from the primary estuaries of Chaohu Lake, Eastern China. The results indicate that the OCP concentrations in the surface and core sediments around Chaohu Lake were 3.48–121.08 (with a mean of 34.93) ng/g and 0.60–39.28 (7.07) ng/g, respectively. Significantly higher concentrations of ΣOCPs were observed in sediment samples from the Nanfei River and its estuary. The three important OCP contributors around Chaohu Lake were dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexane isomers (HCHs), and hexachlorobenzene (HCB), which originated primarily from the historical use of technical DDTs and HCHs. A principal component analysis (PCA) suggests that HCB and lindane may originate from the same sources, and DDTs were greatly influenced by organic carbon from the soil environment and the impact of urbanization processes.     

Simultaneous quantification of capsaicin and dihydrocapsaicin in rat plasma using HPLC coupled with tandem mass spectrometry

A rapid, simple and sensitive HPLC–ESI–MS/MS method was developed for the simultaneous determination of capsaicin and dihydrocapsaicin in rat plasma. Plasma samples containing capsaicin, dihydrocapsaicin and phenacetin (internal standard) were prepared based on a simple protein precipitation by the addition of two volumes of acetonitrile. The analytes and internal standard were separated on a Zorbax SB-C18 column (3.5 μm, 2.1 mm × 100 mm) with mobile phase of acetonitrile/water (55:45, v/v) containing 0.1% formic acid (v/v) at a flow rate of 0.2 mL/min with an operating temperature of 25 °C. Quantification was performed on a triple quadrupole mass spectrometer equipped with electrospray ionization (ESI) source by selected reaction monitoring (SRM) of the transitions at m/z 306–137 for capsaicin, m/z 308–137 for dihydrocapsaicin and m/z 180–110 for the IS. Linear detection responses were obtained for capsaicin and dihydrocapsaicin ranging from 1 to 500 ng/mL and the lower limits of quantitation (LLOQs) for the two compounds were 1 ng/mL. The intra- and inter-day precisions (R.S.D.%) were within 9.79% for the two analytes, while the deviations of assay accuracies were within ±10.63%. The average recoveries of the analytes were greater than 89.88%. The analytes were proved to be stable during all sample storage, preparation and analytic procedures. The method was successfully applied to the pharmacokinetic studies of capsaicin and dihydrocapsaicin in rats after subcutaneous administration of capsaicin (natural, containing 65% capsaicin and 35% dihydrocapsaicin).     

Perfluorinated Compounds in Aquatic Products from Bohai Bay,Tianjin, China

To understand concentrations of perfluorinated compounds (PFCs) in aquatic products, and risks to human health, concentrations of 12 PFCs were measured in edible tissues of aquatic products collected from Tianjin, China, a typical industrial area on the western Bohai Sea. Perfluorooctane sulfonate (PFOS) was the predominant PFC. Concentrations of PFOS in aquatic products from Tianjin Binhai New Area (TBNA) ranged from <0.10 to 241 ng/g wet weight, with the greatest concentration observed in the edible portions of mullet (Mugil so-iuy Basilewsky). Concentrations of PFOS in mullet from the TBNA were greater than those in other species of lower trophic levels, which suggests biomagnification. Concentrations of PFOS in aquatic products from markets were greater than those of locally farmed or wild marine products. Relatively great concentrations of PFOS were not only observed in products from the rapidly growing industrial areas such as Tangu District (TG) and Hangu District (HG), but also in less industrialized areas like the Dagang District (DG). The results of the hazard assessment indicated that consumption of seawater-farmed fish and market fish posed a greater hazard than wild marine fish or freshwater-farmed fish, but the risk to human health was not great.     

Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography–tandem mass spectrometry

The current paper describes a validated method for the detection and quantification of naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018), an ingredient of a herbal mixture called “Spice”, by means of HPLC–ESI–MS–MS in serum. Lower limit of detection and lower limit of quantification were 0.07 and 0.21 ng/ml, respectively. In 2 subjects who consumed ca. 50 μg/kg of JWH-018 by smoking, the active ingredient was detected by means of the described method. Thereby, the serum concentrations reached values of approx. 10 ng/ml and dropped within 3 h very fast (<10% of the measured maximum concentrations).     

Assessment of persistent organochlorine compounds contamination on the Lake Victoria water and sediments: a case study in Tanzania

The current study was conducted to establish the levels of organochlorine pesticides (OCPs), its degradation products, and indicatory polychlorinated biphenyls (PCBs) in water and sediments from Lake Victoria in Tanzania. Seven indicator PCBs were identified in sediments, and five were identified in water. The PCBs loading ranged from lower than the limit of detection (LOD) to 10.28 µg kg^?1 DW and 0.95 to 2.24 µg l^?1 in sediments and water, respectively. PCBs, CB 138 and CB 153 dominated the load, because of their chemical stability and high degree of chlorination. In addition, ten OCPs were identified in sediments, and seven OCPs were identified in water. The levels of organochlorine compounds in sediments were higher than in water samples, implying that sediments may serve as a sink for these compounds. The presence of these compounds is probably as a result of either historical use, long-range environmental transport or environmental persistence. The levels of organochlorine compounds in the lake water and sediments are below the maximum residue limit set by EU and FAO, except for aldrin and dieldrin. Based on the Threshold Effect Concentration (TEC) for freshwater ecosystems, aldrin and dieldrin are the only OCPs that seem to be a threat to the lake environment.     

Determination of Trace Phthalic Acid Monoesters in Sediments and Soils by GC-MS

A simple procedure for determining trace phthalic acid monoesters (PAMs) in sediments/soils was developed. The method used ultrasonic extraction, silylation derivatization, and GC-MS. After ultrasonic extraction, the supernatants were reextracted with dichloromethane, silylated, and did not require further clean-up before GC-MS analysis. Effects of parameters, such as extraction solvents, pH of water as extraction solvent and sediment/soil properties, on the recovery of PAMs were studied. Five sediments from Tianjin city and one red soil from Jiangxi province were used. The results showed that organic carbon (OC) content played an important role in the recovery of PAMs. The optimal extraction solvent for sediments/soils with >1% of OC content and high CEC was 0.01 M HCl aqueous solution and pure water was better for sediments/soils with <1% of OC content. In 5 g sediment/soil sample (dry weight), the method detection limit (MDL) was below 0.04 ng/g for mono-n-butyl phthalate (MBP) and 0.02 ng/g for mono-(2-ethylhexyl)-phthalate (MEHP). Average recoveries of MBP and MEHP were 81.6%?105.2% and 76.0%?95.6%, respectively, with relative standard deviations ≤ 6.6%. MBP and MEHP in the sediment and soil samples studied were detected at levels of 9.2–57.1 and 13.0–166.7 ng/g, respectively.     

PCB concentrations in sediments from the Gulf of Nicoya estuary, Pacific coast of Costa Rica

Thirty-one sediment samples collected from 1996-2003 from the Gulf of Nicoya estuary on the northwestern coast of Costa Rica, have been obtained for PCB analyses. This is part of the first study to evaluate the PCB contamination in coastal Costa Rica. Overall, the concentrations are low, especially when compared to sediments from more temperate climates and/or sediments from more heavily industrialized areas. Values average less than 3 ng/g dw sediment, however, a few samples contained up to 7 ng/g dw sediment. Sediments with the highest concentrations were located in the Punta Morales area, where muds were sampled from among mangrove roots. The Puntarenas samples had surprisingly low PCB concentrations, likely due to their sandy lithology. The congener distribution within the majority of the samples showed signs of either recent sources or lack of degradation. However, a few sites, specifically some of the inter-gulf islands and more remote samples had congener distributions indicative of airborne contaminants and/or degradation. Considering the presence of airborne PCBs in the Gulf of Papagayo to the north, the lack of airborne PCBs and more varied congener distribution in the Gulf of Nicoya estuary was surprising.     

Determination of doxazosin and verapamil in human serum by fast LC-MS/MS: application to document non-compliance of patients

A rapid and sensitive method using liquid chromatography–tandem mass spectrometry (LC–MS/MS) for simultaneous determination of doxazosin and verapamil in human serum has been developed. Trimipramine-d₃ as an isotopic labelled internal standard was used for quantification. Serum samples were prepared by simple liquid–liquid extraction with mixture of tert butyl methyl ether and ethyl acetate (1:1, v:v). The analytes and internal standard were separated on C18 column using an isocratic elution with 5 mM ammonium formate with 0.02% formic acid and 0.02% formic acid in acetonitrile (55:45, v:v) at a flow rate of 1.1 mL/min. Positive TurboIonSpray mass spectrometry was used with multiple reaction monitoring of the transitions at: m/z 455.3 → 165.2 and 150.2 for verapamil, m/z 452.2 → 344.4 and 247.4 for doxazosin, m/z 298.2 → 103.1 for trimipramine-d₃. Linearity was achieved between 1 and 500 ng/mL (R² ≥ 0.997) for both analytes. An extensive pre-study method validation was carried out in accordance with FDA guidelines. This assay was successfully applied to determine the serum concentrations of doxazosin and verapamil in suspect non-compliance patients.     

Phytoplankton community structure and environment in the Kenyan waters of Lake Victoria

• 1 Phytoplankton species composition, numerical abundance, spatial distribution and total biomass measured as chlorophyll a concentration were studied in relation to environmental factors in September 1994 (dry season) and March 1995 (rainy season), respectively, in the Kenyan waters of Lake Victoria; 103 species were recorded.
• 2 Blue‐green algae (Cyanophyceae) were most diverse, followed by diatoms (Bacillariophyceae), green algae (Chlorophyceae) and dinoflagellates (Dinophyceae).
• 3 Twinspan separated the phytoplankton communities in the Nyanza Gulf and those in the open lake during both seasons. During the dry season, the Nyanza Gulf was strongly dominated by blue‐greens, while diatoms dominated in the open lake. During the rainy season, blue‐greens remained dominant in the Nyanza Gulf although the number of species found was lower than during the dry season; in the open lake, blue‐greens replaced diatoms as the dominant group and there were more species than in the dry season.
• 4 Canonical correspondence analysis indicated that the phytoplankton species distribution was significantly correlated with turbidity during the dry season and with SiO₂ during the rainy season. Chlorophyll a concentrations ranging from 2.0 to 71.5 mg m^‐3 in the dry season and 2.0–17.2 mg m^‐3 in the rainy season confirm earlier reports of increasing phytoplankton biomass in Lake Victoria since the 1960s.

     

南淝河沉积物中半挥发性有机污染物分析

采用GC/MS对南淝河沉积物中半挥发性有机污染物进行了分析,共检测出包括多环芳烃和酞酸酯在内的有机化合物有54种,沉积物中有机污染物种类多。对EPA优先控制污染物中的16种多环芳烃（PAHs）进行了定量监测,结果表明多环芳烃的总量已达到30.61mg/Kg。与国外生态风险评价标准对比表明有多种多环芳烃化合物的含量超过风险评价指标的低值,有的甚至超过高值,已有可能对生态环境产生了影响,为较高生态风险区,PAHs污染比较严重。     

Polycyclic aromatic hydrocarbons in surficial sediments and caged mussels of the St. Marys River, 1985

During 1985, a biological monitoring study was conducted in the St. Marys River to determine the availability and source areas of polycyclic aromatic hydrocarbons (PAHs) and the relative importance of water and sediment to tissue contaminant concentrations. Clean unionid mussels (Elliptio complanata) were exposed in cages for three weeks at 14 stations and surficial sediments were obtained at 12 of these. The highest concentrations of total PAHs as well as many individual compounds were found in sediments and mussels from the Algoma Steel Slip above St. Marys Falls and in sediments below the discharge of the Edison Sault Electric Co. Canal. Although concentrations were lower below the Falls, elevated levels persisted downstream along the Ontario shore into Lake George. PAHs were also accumulated by mussels exposed along the Michigan shoreline, but at lower levels than along the Ontario shore. From 23 to 63 percent of the PAHs in sediments and 6 to 27 percent of those in mussels were comprised of compounds with mutagenic and/or carcinogenic properties. The predominance of higher molecular weight PAHs in both sediments and mussels as well as lower molecular weight PAHs and nitrogen- and sulfur-containing PAHs in certain areas, indicates that high temperature combustion of fossil fuels is the major source of PAHs, augmented by localized spills of fossil fuels and coke oven by-products.Mussels contained fewer PAHs (up to 18 vs. 25) at lower concentrations (µg kg^-1 vs. mg kg^-1) than the associated surficial sediments. Also, mussels suspended at mid-depth in the water column accumulated similar concentrations to those exposed to sediments, indicating that the major exposure pathway is via the water filtered by these organisms, and hence, is due primarily to external industrial inputs.