Analysis of trace organic contaminants in sediment,pore water,and water samples from Onsan Bay,Korea: instrumental analysis and in vitro gene expression assay

Persistent organic pollutants and alkylphenols (APs) were determined in sediment and water samples from Onsan Bay, Korea, by using instrumental analysis and in vitro gene expression cell bioassay. Polycyclic aromatic hydrocabons (PAHs) were the predominant compounds in sediments with concentrations as great as 573 ng/g dry weight. The PAH concentrations were elevated in sediment from inland rivers that flow through Onsan City (mean: 116 ng/g dry wt) and discharge into Onsan Bay. Concentrations of polychlorinated biphenyls (PCBs) in sediments ranged from <1.00 to 56.2 ng/g dry weight. Among different organochlorine (OC) pesticides analyzed (hexachlorobenzene, hexachlorocyclohexanes, chlordanes, and DDTs), DDT concentrations were the greatest, ranging from <0.01 to 7.58 ng/g dry weight. The spatial gradient of contaminant concentrations suggested that streams and rivers are the major sources of PCBs, PAHs, and APs to the bay. Maximum concentrations of nonylphenol, octylphenol, and bisphenol A in sediments were 860, 11, and 204 ng/g dry weight, respectively. Screening of Onsan Bay sediment samples for dioxinlike activity with the H4IIE-luc in vitro cell bioassay revealed that 17 of 22 samples contained significant dioxinlike activity. Further fractionation of sediment extracts indicated that mid-polar and more polar fractions were responsible for the significant dioxinlike activity. Based on a mass balance analysis, PAHs apparently accounted for only a small portion of dioxinlike responses elicited by sediment extracts. Only one raw extract of sediment elicited a significant estrogenic response by MVLN cells. The combination of instrumental analysis and in vitro bioassay was useful to assess sediment quality and characterize the causative agents or potential toxic compounds present.     

Occurrence and Partitioning of Phenolic Endocrine-Disrupting Chemicals (EDCs) Between Surface Water and Suspended Particulate Matter in the North Tai Lake Basin, Eastern China

Concentrations and distribution of octylphenol (OP), nonylphenol (NP), and bisphenol A (BPA) in surface water and suspended particulate matter (SPM) from the north Tai Lake basin, China were studied. Aqueous and particulate (dry weight) concentrations for OP, NP, and BPA varied from 10.5–1,175 ng/L to <1.52–5,365 ng/g, respectively. The spatial distribution of endocrine-disrupting chemicals (EDCs) in dissolved and particulate phases showed that the amount of EDCs in water that were adsorbed to SPM gradually increased from upstream to downstream. There were good correlations between particulate EDCs and particulate organic carbon, with correlation coefficients of 0.46–0.57. Regression analysis of in situ SPM–water partition coefficients (log K’ _oc) and log K _ow for EDCs indicated that the hydrophobicity of chemicals greatly contributed to their SPM–water partitioning. Strong positive correlations (r = 0.68–0.82) among in situ log K’ _oc of OP, NP, and BPA and flow velocity of water were observed, indicating the critical importance of riverine hydrodynamics on the sorption of these compounds.     

Residues of Organochlorines in Sediments and Tilapia Collected from Inland Water Systems of Hong Kong

The levels and patterns of organochlorines including DDTs, HCHs, and PCBs were investigated in sediments and tilapia (Tilapia mossambica) collected from inland water systems [Tai Wai (S1), Fo Tan (S2), Siu Lek Yuen (S3), Tai Po (S4), and Tai Wo (S5)] in the New Territories of Hong Kong. Sediment and tilapia samples were also collected from two fish ponds for comparison. The ranges of DDTs, HCHs, and PCBs in river sediments were 2.82–8.63 ng/g (DW), 0.05–2.07 ng/g (DW), and 43–461 ng/g (DW), respectively. All these values were significantly higher (p < 0.05) than the pond sediments. Low chlorinated congeners (especially mono-, tri-, and tetrachlorobiphenyls) were enriched in sediment samples accounting for 70–80% of total PCBs.  The ranges of DDTs, HCHs, and PCBs in tilapia muscle collected from Fo Tan and Tai Wai were 28.2–40.1 ng/g (DW), 2.04–3.76 ng/g (DW) and 267–310 ng/g (DW), respectively. These values were also significantly higher (p < 0.05) than those collected from the fish ponds. Higher chlorinated PCBs (tetra-, penta-, hexa-, and heptachlorobiphenyls) were commonly found in tilapia accounting for almost 60% of the total PCBs. The effect of lipid contents in organochlorines accumulation was not significant (p < 0.05) in general. Received: 24 July 1998/Accepted: 18 November 1998     

Quantification and Source Identification of Polycyclic Aromatic Hydrocarbons in Core Sediments from Sundarban Mangrove Wetland, India

The distribution and potential sources of 16 polycyclic aromatic hydrocarbons (PAHs) in sediment cores (<63 μm particle size) of the Sundarban mangrove wetland, northeastern coast of Bay of Bengal (India), were investigated by gas chromatography coupled to mass spectrometry. The total concentrations of 16 PAHs (∑₁₆PAHs) ranged from 132 to 2938 ng/g, with a mean of 634 ng/g, and the sum of 10 out of 16 priority PAHs (∑₁₀PAH) varied from 123 to 2441 ng/g, with a mean of 555 ng/g, and the 5 carcinogenic PAHs (benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, indeno[1,2,3-cd]pyrene, and dibenz[a,h]anthracene) accounted for 68–73% of the priority PAHs. Maximum concentrations of the sediment core were obtained at subsoil depth of 12–16 cm. The prevalence of four to six aromatic ring PAHs and cross-plots of specific isomer ratios such as phenanthrene/anthracene, fluoranthene/pyrene, and methylphenanthrenes/phenanthrene suggested the predominance of wood and coal combustion sources, the atmospheric deposition, and surface runoff to be the major transport pathways. A good correlation existed between the benzo[a]pyrene level and the total PAH concentrations, making this compound a potential molecular marker for PAH pollution. Total TEQ_S^carc values calculated for samples varied from 6.95 ng/g TEQ_S^carc to 119 ng/g TEQ_S^carc, with an average of 59 ng/g dry weight TEQ_S^carc. The baseline data can be used for regular monitoring, considering the industrial and agricultural growth around this coastal environment.     

Chlorinated Polycyclic Aromatic Hydrocarbons in Sediments from Industrial Areas in Japan and the United States

Chlorinated polycyclic aromatic hydrocarbons (ClPAHs) are widespread environmental pollutants in the urban environment. Nevertheless, there is little information available regarding the occurrence and profiles of ClPAHs in environmental matrices. In this study, residual concentrations and profiles of 20 individual ClPAHs and 16 US EPA-priority PAHs were determined using high- resolution gas chromatography–high-resolution mass spectrometry in sediments from water bodies near industrialized areas: Tokyo Bay, Japan; the Saginaw River watershed, Michigan, USA; a former chlor-alkali plant, Georgia, USA; and the New Bedford Harbor Superfund site, Massachusetts, USA. A sediment core from Tokyo Bay showed temporal patterns in the distribution of ClPAHs from the 1950s through 2004. The fluxes of ClPAHs and 16 priority PAHs in Tokyo Bay sediment core were 0.029–0.57 ng/cm²/year and 85-609 ng/cm²/year, respectively; fluxes were lowest in the 1950s and highest in 1989–1990. In the United States, a high mean concentration of ClPAHs was found in sediment collected near a former chlor-alkali plant [8820 pg/g dry weight (dry wt)], and lower mean concentrations were found for New Bedford Harbor (1880 pg/g dry wt) and the Saginaw River watershed (1140 pg/g dry wt). Among individual ClPAHs, 6-ClBaP and 1-ClPyr were the dominant compounds in sediments; this pattern is similar to the pattern reported in the literature for waste incineration and ambient urban air samples. Significant correlation between ΣClPAH concentrations and Σparent-PAH concentrations in Tokyo Bay sediment implies that the sources and distribution of ClPAHs are directly related to those of parent PAHs. We also analyzed ClPAHs and parent PAHs in blue mussels from New Bedford Harbor. The mean concentration of ClPAHs in mussels from New Bedford Harbor was 21 ng/g lipid weight, a concentration three orders of magnitude lower than the mean concentration of parent PAHs. Low-molecular-weight ClPAHs predominated in mussel tissues. Toxic equivalents (TEQs) of ClPAHs analyzed in sediment ranged between 1.1 fg TEQ/g dry wt (Tokyo Bay) and 2.4 fg TEQ/g dry wt (Saginaw River watershed). The dioxinlike toxicity contributed by ClPAHs in sediment from contaminated areas was five orders of magnitude lower than that previously reported for dioxins.     

Estrogenic Compounds and Estrogenicity in Surface Water,Sediments, and Organisms from Yundang Lagoon in Xiamen,China

Seven estrogenic compounds—estrone (E1), 17β-estradiol (E2), 17α-ethynylestradiol (EE2), diethylstilbestrol (DES), nonylphenol (NP), octylphenol (OP), and bisphenol A (BPA)—in sediments, surface water, pore water, and organisms were investigated and estrogenic activities were estimated by examining estradiol equivalent (EEQ) concentrations in Yundang Lagoon of Xiamen. The results showed that estrogenic compounds were present in all matrixes of interest: in surface water, ranging from 609.61 to 711.31 ng/l; in pore water, ranging from 562.12 to 1038.15 ng/l; in sediments, ranging from 1433.12 to 2060.41 ng/g; and in biota samples, ranging from 1373.76 to 3199.09 ng/g (lipid weight). NP was the predominant component in all collected samples and the highest concentration was 1964.80 ng/g in sediment. Total EEQ ranged from 4.56 to 13.79 ng/l in surface water, from 2.40 to 17.16 ng/l in pore water, and from 8.66 to 23.95 ng/g in sediments. However, major contributors to total EEQ concentrations were E2, E1, and DES. The EEQ concentrations in surface water samples were at a higher level in comparison to that reported in European countries. To biological sample, the highest level of total estrogenic compounds was found in the short-necked clam. Higher values of the biota–sediment accumulation factor (BSAF) were found in short-necked clam and black seabream, indicating that the living habits of organism and physical–chemical properties of estrogenic compounds might influence the bioavailability of estrogenic compounds in organisms.     

Bisphenol A, 4-tert-Octylphenol,and 4-Nonylphenol in The Gulf of Gdańsk (Southern Baltic)

The organic derivatives of phenol are classed as dangerous compounds, and their presence has been detected in surface water, bottom water, phytoplankton, zooplankton, and mussel as well as liver and muscle of fish from the Gulf of Gdańsk and in liver, muscle, and guano of gulls residing in the coastal zone of this basin. The greatest sources of bisphenol A (BPA), 4-tert-octylphenol (OP), and 4-nonylphenol (NP) were found to be the Vistula River and the water purification plant in D?bogórze. In living organisms, concentrations of BPA, OP, and NP ranged between the limit of quantification and several hundred ng g^?1 dry weight (dw), and the highest concentrations were found for BPA. Prolonged alimentary exposure to BPA, OP, and NP in fish and birds was indicated by liver/muscle concentration ratios generally >1. The most influential factors on BPA and alkylphenol concentrations in the tissues of fishes and gulls were mainly diet and habitat. The study confirmed possible bioaccumulation in the food web. High BPA and NP concentrations in guano (≤2,700 and ≤300 ng g^?1 dw, respectively) indicated the ability of birds to detoxify and signalled the reintroduction of these compounds to seawater. Herring, flounder, and cod from the Southern Baltic are a safe food source for human consumption because their BPA and alkylphenol contents are low.     

Polychlorinated naphthalenes, biphenyls, dibenzo-p-dioxins, and dibenzofurans as well as polycyclic aromatic hydrocarbons and alkylphenols in sediment from the Detroit and Rouge Rivers, Michigan, USA

Sediment from the upper Detroit and lower Rouge Rivers in southeastern Michigan, USA, were analyzed to examine the distribution of polychlorinated naphthalenes (PCNs), biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), and dibenzofurans (PCDFs) as well as polycyclic aromatic hydrocarbons (PAHs) and alkylphenolic compounds such as butylphenol, octylphenol, and nonylphenol (NP). Sediments from a non-point source location in Lake Michigan were also analyzed for target compounds. Concentrations of target compounds in the upper Detroit and lower Rouge Rivers varied considerably among locations, and notable spatial variation existed. Concentrations of PCNs and PCDDs/PCDFs in sediments from the upper Detroit and lower Rouge Rivers ranged from 0.08 to 187 ng/g and 69 to 1420 pg/g dry weight, respectively. Total PCBs, PAHs, and NP concentrations ranged from 8 to 25,000, 17 to 44,000, and < 10 to 60,000 ng/g dry weight, respectively. Concentrations of all target compounds except PCNs were significantly correlated with total organic carbon content of sediments. Similarly, concentrations of PCBs, PCDDs, and PCDFs were significantly correlated with each other. The distribution of organic contaminants in the upper reaches of the Detroit River and lower Rouge River suggested the presence of localized, but multiple, sources of contamination for each compound class. Conners Creek combined sewer overflow has been identified as one of the potential sources for the upper Detroit River, where the highest concentrations PCBs and PCDDs/PCDFs were found. Polycyclic aromatic hydrocarbon and NP concentrations were consistently high in sediment from the lower Rouge River. Analysis of data from selected locations suggested that PCNs contributed a greater proportion of the dioxin-like activity than PCBs and PCDDs/PCDFs contributed.     

Polychlorinated Biphenyls and Organochlorine Pesticides in Human Adipose Tissue and Breast Milk Collected in Hong Kong

Contamination from persistent organic pollutants is a pervasive global problem that urgently demands global concern and action. In the present study, concentrations of organochlorine (OC) pesticides and polychlorinated biphenyls (PCBs) were determined in 37 samples of female adipose tissue collected in Hong Kong hospitals. Among the pollutants analyzed, DDTs (2.79 ng/g fat), HCHs (0.72 ng/g fat), and PCBs (0.19 ng/g fat) were prominent compounds in most of the adipose tissue. p,p′-DDE and hexachlorinated biphenyls were found in all samples, whereas heptachlor epoxide and dieldrin were found only in some samples. An estimation of toxic equivalency concentration (TEQ) due to dioxin-like coplanar PCBs was also performed. The estimated TEQ_PCBs was 2.01 pg/g fat. This study also compared our previous results obtained from the milk samples of the same donors. Significant correlations are obtained for DDTs and HCHs between milk and adipose tissue. Detailed review of available information concerning OC pesticides and PCBs in different ecological compartments indicated that bioconcentration and biomagnification of these contaminants are common phenomena of the Pearl River Delta region, which has undergone rapid socioeconomic change in the past 20 years. It is suggested to establish a regional organization in order to coordinate the monitoring of persistent organic pollutants in the region.     

The Effects of Nonylphenol and Octylphenol on Embryonic Development of Sea Urchin (<Emphasis Type="Italic">Paracentrotus lividus</Emphasis>)

In this study, embryotoxic and genotoxic effects of nonylphenol (NP) and octylphenol (OP), which are the derivates of alkylphenol (APs), were evaluated using the gametes and embryos of the sea urchin Paracentrotus lividus. The sperm and eggs of sea urchins were exposed to increasing concentrations of NP (0.937–18.74 μg/L) and OP (5–160 μg/L) under static conditions. The endpoints were sperm fertilization success, quantitative and morphologic changes in mitotic activity, larval malformations, developmental arrest, and embryonic/larval mortality. A dose–response-related reduction (approximately 20%) was observed in fertilization success and significant increases in the number of larvae with skeleton malformations at the pluteus stage of the contaminated sperms. The spermiotoxic and embryotoxic concentrations were determined as 0.937 μg/L for NP and 4.685 μg/L for OP for this species. The embryotoxicity of NP and OP is concentration dependent, and significant growth reduction at the early life stages and an increase in larval malformations as skeleton deformities at the pluteus stage were observed. Cytogenetic analysis of embryos showed a decreasing curve in mitotic indexes (number of mitosis per embryo) with increasing concentrations of NP and OP. It can be concluded that NP and OP adversely affect the reproduction and embryonic developmental stages of the P. lividus and this is of great ecological importance because of the hazard at the population level.     

Polynuclear aromatic and chlorinated hydrocarbons in mussels from the coastal zone of Ushuaia, Tierra del Fuego, Argentina

Mussels (Mytilus edulis chilensis) were collected from 12 coastal locations in Ushuaia Bay, Argentina, and the surrounding area in October 1999 and again in October 2003. Concentrations of polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and selected chlorinated pesticides were determined to assess the impact of a fast-growing population in the area. Total PAH concentrations ranged from 2.24 to an extremely high concentration of 2,420 μg/g lipid measured in mussels collected near an oil jetty used to discharge to shore storage tanks. The composition of PAHs in these samples indicates that the source of these compounds inside Ushuaia Bay is predominantly petrogenic, with some pyrogenic background, whereas mostly pyrogenic-related PAHs were evident in areas outside the bay. Total concentrations of PCBs ranged between 12.8 and 8,210 ng/g lipid, with the highest concentration, detected inside Ushuaia harbor, representing a 10-fold increase when compared with historical data. Chlorinated pesticides were detected at comparatively lower concentrations, with 4-4'- 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene being the most common. The aggressive increase in population and related activities observed in the city of Ushuaia over the last two decades might have affected the environmental quality of the local bay. Moreover, the oceanographic and atmospheric conditions existing in Ushuaia Bay and surrounding areas may favor the accumulation and long-term presence of these organic pollutants in all compartments of this fragile environment.     

Dioxin-Like Toxicity in the Saginaw River Watershed: Polychlorinated Dibenzo-<Emphasis Type="Italic">p</Emphasis>-Dioxins,Dibenzofurans, and Biphenyls in Sediments and Floodplain Soils from the Saginaw and Shiawassee Rivers and Saginaw Bay,Michigan, USA

Sediment and floodplain soils in the Saginaw River Watershed, Michigan, USA, have been demonstrated to be contaminated with a variety of organic compounds, including polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins (PCDDs), and polychlorinated dibenzofurans (PCDFs). Existing data indicate that, at some locations, the contamination exceeds human health risk-based regulatory levels and ecological risk-based screening levels. In this study, concentrations of PCBs including non-ortho coplanar congeners, PCDDs, and PCDFs were measured in more than 120 sediment and floodplain soil samples collected from the Shiawassee River (a tributary of the Saginaw River), the Saginaw River, and Saginaw Bay, to determine the sources and magnitude of contamination, and to elucidate the contributions from individual contaminant groups to the overall 2,3,7,8-tetrachlorodibezo-p-dioxin equivalents (TEQs). Sediment and soil extracts were also analyzed for total dioxin-like activity by means of the H4IIE-luc cell bioassay. Elevated concentrations of PCBs (>1000 ng/g, dry weight) were found in surface sediment and floodplain soil samples collected from the Shiawassee River near Chase Lake, from Middleground Island in the Saginaw River, and from subsurface sediments in Saginaw Bay. Concentrations of PCDDs and PCDFs in sediment and floodplain soils from the Saginaw River and Saginaw Bay were 2 to 3 orders of magnitude higher than concentrations in the samples from the Shiawassee River. The highest PCDD/F concentration (55,200 pg/g, dry weight in a subsurface layer) was found in sediment collected at the mouth of the Saginaw River. Concentrations of PCDFs were greater than the concentrations of PCDDs in sediment from the Saginaw River. 2,3,7,8-TCDF, 1,2,3,7,8-PeCDF, and 2,3,4,7,8-PeCDF were the major PCDF congeners found in sediments from the Saginaw River. The elevated concentrations of PCDFs, and the predominance of the less highly chlorinated PCDF congeners, in sediments from the Saginaw River were similar to previously determined characteristics of the PCDF contamination of the Tittabawassee River, another tributary of the Saginaw River. These results suggest the existence of a major source of PCDFs within the watershed. A few localized areas of high PCDD/F and PCB concentrations, with unique congener compositions, in the Saginaw River indicated the presence of other minor sources, such as wastewater treatment plants. PCDFs were the major contributors to TEQs in sediment and soils from the Saginaw River and Saginaw Bay. Approximately 30% of the samples analyzed in this study had values exceeding the screening level of 50 pg TEQ/g, dry wt, suggested for soils by the Agency for Toxic Substances and Disease Registry.     

Organochlorine Pesticides and Polychlorinated Biphenyls (PCBs) in Sediments and Biota from Four US Arctic Lakes

Organochlorine (OC) concentrations in surface sediment, snails (Lymnea sp.), and two freshwater fish species (grayling, Thymallus arcticus; and lake trout, Salvelinus namaycush) from four lakes in the US Arctic were determined. In surface sediment, chlorinated benzenes (including hexachlorobenzene, HCB), and p,p′-DDT were the primary analytes detected (max = 0.7 ng/g dry wt), while individual polychlorinated biphenyl (PCB) congeners were always below 0.1 ng/g. A wider range of compounds and higher concentrations were found in lake trout, the top predatory fish species in the same lakes. The concentration ranges for hexachlorocyclohexanes (HCHs), chlordane-related compounds (CHLORs), DDTs, and PCBs in lake trout and grayling were similar to those reported for other arctic freshwater fish (1–100 ng/g wet wt), but one to two orders of magnitude lower than Great Lakes salmonids. Nitrogen isotope analysis confirmed that differences in OC concentrations between grayling and lake trout are explained partly by differences in food web position. Received: 30 August 1996/Accepted: 24 July 1997     

In Vitro Bioassay Determination of Dioxin-Like and Estrogenic Activity in Sediment and Water from Ulsan Bay and Its Vicinity, Korea

Extracts of sediment and water samples collected from Ulsan Bay, Korea, were screened for their ability to induce dioxin-like and estrogenic gene expression in vitro. Each sample was tested as raw extract (RE) and fractionated extract (FE). Based on the initial screening of RE, 23 of 31 sediment samples showed significant dioxin-like activity in H4IIE-luc bioassay, whereas most sediment samples did not elicit estrogenic response in MVLN bioassay. Most of the activities associated with FE samples revealed that mid-polar (F2) and most polar (F3) fractions were responsible for the significant reporter gene expression in H4IIE-luc bioassay. The results suggest that complex interactions may have depressed the activities of the known arylhydrocarbon receptor (AhR) agonists present in F1 samples. The F2 samples were the most active fraction. All F2 samples except one induced significant dioxin-like activity, and over half of the F2 samples induced significant estrogenic activity. Ten of the F2 samples produced magnitudes of response in H4IIE-luc bioassay similar to those induced by a 2,3,7,8-tetrachlorodibenzo-p-dioxin standard. Sediment associated with F2 samples was estimated to contain 24.9–826 pg TCDD-EQ/g DW. Based on a qualitative mass balance analysis, polycyclic aromatic hydrocarbons (PAHs) appeared to account for both the estrogenic and dioxin-like responses observed. Over half of the F3 samples were either cytotoxic or caused morphological changes in both H4IIE-luc and MVLN cells. Known concentrations of alkylphenols and bisphenol A were not great enough to account for both the estrogenic response and cytotoxicity observed for F3 samples. Despite the apparent toxic or stressful effects, most of F3 samples induced significant dioxin-like activity in vitro, adding to a growing body of evidence that suggests the presence of unidentified, relatively polar, AhR agonists in sediment from some areas. Received: 11 June 2000/Accepted: 28 August 2000     

Relationship between lysosomal membrane destabilization and chemical body burden in eastern oysters (Crassostrea virginica) from Galveston Bay,Texas, USA

Lysosomal destabilization was measured by using hemocytes of eastern oysters (Crassostrea virginica) collected along a chemical concentration gradient in Galveston Bay, Texas, USA. Results of the lysosomal response were compared to concentrations of organic compounds and trace elements in oyster tissue. Concentrations (on a dry-wt basis) ranged from 288 to 2,390 ng/g for polycyclic aromatic hydrocarbons (PAHs), 38 to 877 ng Sn/g for tri-n-butyltin (TBT), 60 to 562 ng/g for polyclorinated biphenyls (PCBs), and 7 to 71 ng/g for total DDT. Trace element concentrations (on a dry-wt basis) ranged from 1.1 to 4.0 microg/g for Cd, 105 to 229 microg/g for Cu, 212 to 868 microg/g for Al, and 1,200 to 8,180 microg/g for Zn. The percentage of destabilized lysosomes ranged from 34 to 81%. A significant positive correlation (p < 0.05) was observed between lysosomal destabilization and body burden of organic compounds (PAHs, PCBs, TBT, and chlorinated pesticides). No significant correlation was found between metal concentrations and lysosomal destabilization. Based on lysosomal destabilization, the study sites in Galveston Bay can be placed in one of three groups: healthy (Hanna Reef and Confederate Bay), moderately damaged (Offats Bayou and Todd's Dump), and highly damaged (Yacht Club and Ship Channel). Lysosomal destabilization that is consistent with toxic chemical body burdens supports previous observations that lysosomal membranes are damaged by toxic chemicals and indicates that this method can serve as an early screening tool to assess overall ecosystem health by using oysters.     

Trace Organic Contaminants,Including Toxaphene and Trifluralin,in Cotton Field Soils from Georgia and South Carolina,USA

Residues of organic contaminants—including toxaphene, DDT, trifluralin, hexachlorocyclohexanes, polychlorinated biphenyls, polycyclic aromatic hydrocarbons (PAHs) and nonylphenol—were measured in 32 cotton field soils collected from South Carolina and Georgia in 1999. Toxaphene, trifluralin, DDT and PAHs were the major contaminants found in these soils. The maximum concentration of toxaphene measured was 2,500 ng/g dry weight. Trifluralin was detected in all the soils at concentrations ranging from 1 to 548 ng/g dry weight. Pesticide residues were not proportional to soil organic carbon content, indicating that their concentrations were a reflection of application history and dissipation rates rather than air–soil equilibrium. Soil extracts were also subjected to in vitro bioassays to assess dioxinlike, estrogenic, and androgenic/glucocorticoid potencies. Relatively more polar fractions of the soils elicited estrogenic and androgenic/glucocorticoid activities, but the magnitude of response was much less than those found in coastal marine sediments from industrialized locations.Received: 23 November 2002/Accepted: 13 January 2003     

Urinary concentrations of bisphenol A and triclosan and associations with demographic factors in the Korean population

Bisphenol A (BPA) and triclosan are synthetic phenolic compounds to which the general public can be extensively exposed via consumer products and environmental contamination.In this study, we assessed exposure to BPA and triclosan in the Korean adult population aged 18–69 based on the Korean National Human Biomonitoring Survey conducted in 2009. Relying on data from 1870 representative Koreans, we found that the geometric mean urinary concentrations of BPA and triclosan were 1.90 ng/ml [95% confidence interval (CI): 1.81–1.99] and 1.68 ng/ml (95% CI: 1.48–1.90), respectively. The creatinine-adjusted geometric means of BPA and triclosan were 1.79 μg/g creatinine (95% CI: 1.70–1.90) and 1.58 μg/g creatinine (95% CI: 1.39–1.81), respectively. About 99.8% of the Korean adult population had urinary concentrations of BPA and about 92.6% of the Korean adult population had urinary concentrations of triclosan above the level of 0.05 ng/ml (limit of detection, LOD). Urinary BPA concentrations were higher in residents of rural areas, whereas urinary triclosan concentrations were significantly associated with cigarette smoking. These findings suggested that most Koreans had detectable levels of BPA and triclosan in their urine and that the body burden of BPA and triclosan varied according to demographic and geographic factors.     

Nonylphenol and Nonylphenol Ethoxylates in Fish,Sediment, and Water from the Kalamazoo River,Michigan

A survey measuring concentrations of nonylphenol (NP) and its ethoxylates (NPEs) in fish was performed in the Kalamazoo River, Michigan, USA, in 1999. Of 183 fish analyzed, 59% had no detectable NP or NPE. Detected concentrations were reported to range from 3.3 (limit of detection) to 29.1 ng NP/g wet weight. To further explore the means of exposure of NP and NPE in the fish, concentrations of NP and its mono-through tri-ethoxylates (NPE_1–3) were measured in fish, sediment, and water collected near two wastewater treatment plants on the Kalamazoo River in 2000. Samples were analyzed using exhaustive steam distillation with concurrent liquid extraction. Nonylphenol ethoxycarboxylates (NPE_1–3C) were also analyzed in water. Concentrations of NP and NPEs in fish were less than the method detection limits (MDLs) in all the samples except one fish, which contained 3.4 ng NP/g wet weight, just above the detection limit of 3.3 ng/g. Three of 36 sediments and 1 of 24 water samples contained detectable concentrations of NP or NPE₁. NPE₂, NPE₃, and NPEC were not detected in water samples. Received: 18 December 2001/Accepted: 13 May 2002     

Distribution and Sources of Aliphatic and Polycyclic Aromatic Hydrocarbons in Surface Sediments,Fish and Bivalves of Abu Qir Bay (Egyptian Mediterranean Sea)

Polycyclic aromatic hydrocarbons (PAHs) were detected and quantified in recent marine sediments and selected species from fishes, bivalves and crustaceans of Abu Qir Bay during the period January–October 2004. Nineteen sampling stations were chosen to collect sediment samples covering almost the Bay area. Total PAHs found in the surficial bottom sediments of the Bay were identified in moderate values ranging between 69 and 1,464 ng/g dry weights. The distribution pattern of these compounds showed the availability of most di, tri- and tetra aromatics in the Bay area in addition to their alkyl derivatives. High molecular weight aromatic hydrocarbons of five or more ring were detected everywhere in the Bay sediments. Certain number of pairs of isomer PAH concentrations are used for five origin molecular indices to identify the PAH concentration sources in the sediments of the Bay: Fluo/Py, Fluo/[Fluo + Py], LMW/HMW, BbF/BaP and BkF/BaP. Abu Qir Bay sediment samples were contaminated mainly by pyrolytic and petrogenic contaminations with strong pyrolytic inputs in the southwestern basin, while the northeastern area of the Bay is contaminated mainly by petrogenic PAHs. The studied biota samples of the Bay revealed levels of moderately contaminated specimens with total PAHs, while the carcinogenic PAH, benzo(a)pyrene were detected in most biological samples in levels ranged between 30.3 and 358 ng/g with an average of 152.4 ng/g should be taken into consideration.     

Estrogenic compounds in seawater and sediment from Halifax Harbour, Nova Scotia, Canada

Abstract-Samples of seawater and surface sediment were collected from seven locations around Halifax Harbour, Nova Scotia, Canada, and analyzed for the presence of the organic estrogenic contaminants, bisphenol A (BPA), 17beta-estradiol (E2), and 17alpha-ethinylestradiol (EE2). Samples were extracted using solid phase extraction (seawater) or sonication (sediments), followed by fractionation on a two-layer alumina/silica gel column prior to analysis by liquid chromatography-tandem mass spectrometry (LCMS/MS) with negative-ion electrospray ionization. Levels of the three compounds consistently ranked as BPA > E2 > EE2. The least potent compound and plasticizer BPA reached levels of up to 2.6 ng/L in seawater and 9.5 ng/g in sediments; the natural product E2 was detected at concentrations up to 0.57 ng/L and 0.86 ng/g; while the synthetic estrogen EE2 was in most cases below the method detection limit (0.14 ng/L and 0.28 ng/g). The highest levels were observed in the influent of a secondary treatment plant that discharges into the harbor, with concentrations of 32.4 ng/L for BPA and 5.3 ng/L for E2. Overall, the results indicate that these compounds readily associate with suspended particles rather than remaining in the soluble phase. Measurement of the octanol-water partition coefficient (log K(OW)) confirmed these results, with values of 3.41, 3.89, and 4.16 for BPA, E2, and EE2, respectively. Partitioning experiments using spiked field samples further confirmed these findings, with sorption directly related to sediment total organic content and following the order EE2 > E2 > BPA.