Polychlorinated Biphenyls Concentrations In Sediments Research Articles

Assessment of exposure of benthic organisms to selected organochlorine pollutants in the west Spitsbergen fjords

Climate-related changes in environmental conditions, such as reduction of sea ice, intensive glacier retreat, and increasing summer precipitation, directly influence the arctic marine environment and, therefore, the organisms living there. Benthic organisms, being an important food source for organisms from higher trophic levels, constitute an important part of the Arctic trophic network. Moreover, the long lifespan and limited mobility of some benthic species make them suitable for the study of the spatial and temporal variability of contaminants. In this study, organochlorine pollutants (polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB)) were measured in benthic organisms collected in three fjords of western Spitsbergen. Two of these were recommended by the Marine Biodiversity and Ecosystem Functioning (MARBEF) Network of Excellence as European flagship sites, namely Hornsund as the Biodiversity Inventory and Kongsfjorden as the Long-Term Biodiversity Observatory. Adventfjorden, with notable human activity, was also studied. Ʃ7 PCB and HCB concentrations in sediments were up to 2.4 and 0.18 ng/g d.w. respectively. Concentrations of Ʃ7 PCBs and HCB measured in collected benthic organisms were up to 9.1 and 13 ng/g w.w., respectively. In several samples (41 of 169) the concentrations of ∑7 PCBs were below the detection limit values, yet nevertheless the results of the research show effective accumulation of target organochlorine contaminants by many Arctic benthic organisms. Important interspecies differences were observed. Free-living, mobile taxa, such as shrimp Eualus gaimardii, have accumulated a large quantity of contaminants, most probably due to their predatory lifestyle. ∑7 PCB and HCB concentrations were both significantly higher in Hornsund than in Kongsfjorden. Biomagnification occurred in 0 to 100 % of the predator-prey pairs, depending on the congener analyzed. Although the sampled organisms were proved to have accumulated organochlorine contaminants, the measured levels can be considered low, and not posing a substantial threat to the biota.

Monitored Natural Recovery of Contaminated Sediment in Cottonwood Bay, Texas

ABSTRACT Monitored natural recovery (MNR) is a response action for contaminated sediment that relies on natural processes to reduce ecological and human health risks to acceptable levels over time. Multi-media long-term monitoring is necessary to verify remedy effectiveness and success. Whereas MNR has most often been employed together with other engineered remedies to address contaminated sediment, this case study describes an evaluation demonstrating the suitability of MNR with adaptive management as a stand-alone sediment remedial strategy for Cottonwood Bay, located in Dallas, Texas. Current risks at the Cottonwood Bay site are associated with human consumption of fish contaminated with polychlorinated biphenyls (PCBs). The lines of evidence used to evaluate MNR included documentation of source control; review of PCB burial/isolation and surface sediment recovery; evaluation of sediment deposition and sediment stability; and demonstration of decreasing temporal trends in fish tissue PCB concentrations. The multiple lines of evidence demonstrated that source control and natural recovery processes have contributed substantially to reduced concentrations of PCBs and metals in surface sediments and PCBs in fish. MNR has been approved by the Texas Commission on Environmental Quality (TCEQ) and is incorporated as a stand-alone remedy in the revised Remedial Action Plan (RAP) for Cottonwood Bay. A long-term monitoring plan is being implemented as part of an MNR response action to confirm decreasing trends in surface sediment and fish fillet PCB concentrations over time and to demonstrate the continued effectiveness of natural recovery processes.

Occurrence and spatial characteristics of polychlorinated biphenyls (PCBs) in sediments from rivers in the western Niger delta of Nigeria impacted by urban and industrial activities

The characteristic concentrations of 28 PCB congeners, their spatial distributions, sources, and associated risks to the ecosystem were investigated in sediments of some rivers around a glass industry and power generating plant in the Niger Delta of Nigeria. Gas chromatography-mass spectrometry (GC-MS) was applied for the identification and quantification of PCBs in sediments from these rivers. The Ʃ28 PCB concentrations (dry weight) in sediments ranged from 1520 to 3540 ng g−1 for the Afiesere River, 976–5670 ng g−1 for the Edor River, and from 1440 to 6340 ng g−1 for the Okpare River. The homologue distribution patterns in sediments from these rivers indicated that low-chlorinated (2 Cl to 5 Cl) PCBs were more dominant than high-chlorinated (6 Cl to 10 Cl) PCBs with tri-, penta- and deca-PCBs as the top homologues. The PCB source analyses suggested that the PCB contamination of these river sediments could have originated from Aroclor mixtures, paints, pigments and other inadvertent sources. The risk assessment indicated a high risk to the ecosystem.

Spatiotemporal trends of polychlorinated biphenyls (PCBs) in surface and suspended sediments from the Lake Ontario Canadian nearshore 1994–2018: A fish consumption advisory perspective

Spatiotemporal trends for polychlorinated biphenyls (PCBs) were examined in surface and suspended sediments collected between 1994 and 2018 from over twenty nearshore stations on the Canadian side of Lake Ontario and the St. Lawrence River. In 2018, PCB concentrations ranged over an order-of-magnitude in surface (<10 ng/g−357 ng/g) and suspended sediments (<10 ng/g–330 ng/g), illustrating the presence of legacy hotspots as well as diffuse urban inputs. PCB concentrations in both surface and suspended sediments were consistently highest in Hamilton Harbour, but were also elevated at other stations around the perimeter of the Niagara basin as well as near Trenton and Kingston, Ontario. Generally, higher PCB concentrations were found in surface sediment relative to paired suspended sediment samples suggesting temporal improvements in nearshore sediment quality. However, many stations demonstrated temporal variability in PCB concentrations, a likely factor in the lack of an overall nearshore declining trend. Given that PCBs are listed as a consumption-limiting contaminant for all fish sampling blocks in the Canadian waters of Lake Ontario and are responsible for 78% of restricted advisories, sediment quality benchmarks that account for bioaccumulation potential should be considered over toxicologically-derived guidelines to gauge severity of PCB contamination of nearshore sediments. Relatively higher TOC-normalized PCB concentrations in the western end of Lake Ontario suggests additional research on PCB bioavailability from nearshore sediment would be beneficial in understanding basinwide trends of PCBs in fish, and that an adaptive approach to sediment management may be needed in the context of consumption advisories.

Terrestrial inputs govern spatial distribution of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) in an Arctic fjord system (Isfjorden, Svalbard).

Considerable amounts of previously deposited persistent organic pollutants (POPs) are stored in the Arctic cryosphere. Transport of freshwater and terrestrial material to the Arctic Ocean is increasing due to ongoing climate change and the impact this has on POPs in marine receiving systems is unknown This study has investigated how secondary sources of POPs from land influence the occurrence and fate of POPs in an Arctic coastal marine system. Passive sampling of water and sampling of riverine suspended particulate matter (SPM) and marine sediments for analysis of polychlorinated biphenyls (PCBs) and hexachlorobenzene (HCB) was carried out in rivers and their receiving fjords in Isfjorden system in Svalbard. Riverine SPM had low contaminant concentrations (<level of detection-28pg/g dw ΣPCB14, 16-100pg/g dw HCB) compared to outer marine sediments 630-880pg/g dw ΣPCB14, 530-770pg/g dw HCB). There was a strong spatial gradient in sediment PCB and HCB concentrations with lowest concentrations in river estuaries and in front of marine-terminating glaciers and increasing concentrations toward the outer fjord. This suggests that rather than leading to increased concentrations, inputs of SPM from land lead to a dilution of contaminant concentrations in nearshore sediments. Preliminary estimates of SPM:water activity ratios suggest that terrestrial particles (with low contaminant concentrations) may have the potential to act as sorbents of dissolved contaminants in the coastal water column, with implications for bioavailability of POPs to the marine food web. There is concern that ongoing increases in fluxes of freshwater, sediments and associated terrestrial material (including contaminants) from land to the Arctic Ocean will lead to increased mobilization and transport of POPs to coastal ecosystems. However, the results of this study indicate that on Svalbard, inputs from land may in fact have the opposite effect, leading to reduced concentrations in coastal sediments and waters.

Spatial characteristics, sources, and ecological and human health risks of polychlorinated biphenyls in sediments from some river systems in the Niger Delta, Nigeria

Polychlorinated biphenyls (PCBs) were quantified in sediments from the lower reaches of the Niger, Ase and Forcados Rivers in Nigeria with the aim of elucidating the sources, spatial characteristics and likely ecological and human health risks relating to exposure to PCBs in the sediments. A total of 28 PCB congeners, including 7 indicator PCBs and 12 dioxin-like PCBs, were identified and quantified after Soxhlet extraction with acetone/n-hexane/dichloromethane by gas chromatography–mass spectrometry. The Σ28 PCB concentrations in sediments from the Niger, Ase and Forcados Rivers ranged from 13.5 to 277 ng g−1, not detected to 1633 ng g−1 and 6.9 to 78.6 ng g−1 respectively. The PCB composition in sediments from these three rivers indicate the dominance of lower chlorinated (2-Cl to 5-Cl) congeners over higher chlorinated (6-Cl to 10-Cl) congeners. The ecological and human health risk assessment suggests potential risks for exposure of both organisms and humans to PCBs in sediments from these three river systems.

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

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

Microplastic pollution in deep-sea sediments and organisms of the Western Pacific Ocean

Microplastics are ubiquitous in marine environments. Sediments and marine organisms are recognized as the carriers and final destinations of microplastics. However, research on the concentration and abundance of microplastics in deep-sea sediments and organisms is limited. In this study, samples of sediments and organisms were collected from deep-sea locations of the western Pacific Ocean, with the depth ranging from 4601 m to 5732 m. Microplastics were extracted from the samples and analyzed by micro-Fourier-transform infrared spectroscopy. The average abundance of microplastics in the sediments was 240 items per kg dry weight of sediment. The microplastics were predominantly fibrous in shape (52.5%), blue in color (45.0%), and less than 1 mm in size (90.0%). The most commonly detected polymers were poly(propylene-ethylene) copolymer (40.0%) and polyethylene terephthalate (27.5%). The concentrations of polychlorinated biphenyls (PCBs), which are representatives of persistent organic pollutants, in the pore water of sediment samples were also investigated. A significant correlation between the distribution of microplastics and the PCB concentrations in sediments was found (P = 0.016). Microplastics were also detected in deep-sea organisms (i.e., Crinoidea, Pheronematidae, Ophiuroidea, and Gammaridea) in the sampling region, with an abundance of 0–3 items per individual biological sample. This assessment of microplastics in deep-sea sediments and benthic organisms of the western Pacific Ocean confirms that microplastic pollution exists in the deep-sea ecosystems of this region.

Distribution and Human Risk Assessment of Polycyclic Aromatic Hydrocarbons (PAHs) and Polychlorinated Biphenyls (PCBs) in Marine Sediments and Seafood from Gunsan Coast of Korea

Distributions of 16 PAHs and 82 PCBs (including dioxin-like PCBs, DL-PCBs, and non-dioxin-like PCBs, NDL-PCBs) were investigated in sediment and seafood samples collected from the Gunsan coast, Korea. Total PAH (Σ16PAH) concentrations in sediments were in a range of 0.09~108 (mean: 57.9) ng/g-dry and gradually decreased outwardly. PAHs in marine sediments were originated from both combustion processes and petroleum sources. The total PCB (Σ82PCB) concentrations in sediments were in a range of nd (not detected)-0.64 (mean: 0.27) ng/g-dry, and DL-PCB (Σ12 dioxin-like PCB) were in a range of nd-0.293 (mean 0.054) pg-TEQ/g-dry. DL-PCB concentrations were correlated with NDL-PCB concentrations. In this study, the concentrations of PAHs and PCBs in marine sediments did not exceed the ecotoxicological values. Total PAH concentrations ranged from nd to 24.3 (mean: 5.35) ng/g-wet, benzo[a]pyrene (BaP) was not detected in seafood samples and the concentrations of Σ4PAH (BaP, chrysene, benzo[a]anthracene, and benzo[b]fluoranthene; nd-18.5 ng/g-wet) were lower than the maximum level (30 ng/g-wet) set by EU. The concentrations of NDL-PCBs in seafood samples were in a range of nd-0.19 (mean: 0.08) ng/g-wet less than 1% of the EU-set maximum level. The DL-PCB concentrations were below 0.1 pg-TEQ/g-wet, less than 1% of the EU-set maximum level. Human risk assessment of PAHs and PCBs via seafood consumption was carried out, and both lifetime cancer risk and non-cancer risk were low. Key Words: PAHs, Dioxin-like PCBs, Sediment, Seafood, Human risk assessment

Polychlorinated biphenyls in stormwater sediments: Relationships with land use and particle characteristics

Polychlorinated biphenyls (PCBs) are classified as persistent organic pollutants (POPs). Concentrations of 209 PCB congeners as well as profiles of the ten homologues were determined in stormwater sediments collected from various (primarily roadway) sites with different land use. The total PCB concentrations ranged from 8.3 to 57.4 ng/g dry weight (dw), with a mean value of 29.2 ng/g dw. PCB concentrations varied with nearby land use. Higher stormwater sediment PCB concentrations were found in dense urban areas (average: 39.8 ± 10.5 ng/g) and residential areas (average: 35.3 ± 6.2 ng/g) compared to highways passing through greenspace (average: 18.0 ± 0.4 ng/g). The number of chlorines per biphenyl ranged from 3.63 to 5.39 and the toxic equivalency (TEQs) of the PCBs were between 1.5 and 18.0 pg/g at all sites. A non-Aroclor congener, PCB 11, was detected in all samples and was dominant at two sites. PCBs were sorbed to smaller stormwater particulate matter (≤75 μm) at higher concentrations compared to larger particles (>75 μm). PCB sorption tended to increase with the total organic carbon (TOC) of the particulate matter in the sediment samples. However, greater PCB mass (almost 80%) was present in the larger particles. Information on sediment PCB concentrations from different land uses, along with stormwater particulate matter data can allow the estimation of PCB loads and load reductions using stormwater control measures.

Bioaccumulation and cycling of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in three mangrove reserves of south China

Total 22 organochlorine pesticides (OCPs) compounds and 31 polychlorinated biphenyls (PCBs) congeners in mangrove sediments and tissues (leaf, branch, root and fruit) of nine species from three Mangrove Reserves of China were studied. The mean concentrations of total DDTs, HCHs, OCPs and PCBs in sediments were 2.84, 0.06, 3.84 and 0.17 ng g−1 dw, while those in tissues were 1.85, 0.22, 9.43 and 1.61 ng g−1 dw, respectively. The elevated OCPs and PCBs levels in mangrove leaves may be caused by atmospheric sedimentation. The biota sediment accumulation factor (BSAF) values of both OCPs (mean: 3.4) and PCBs (mean: 9.9) are generally larger than one, implying mangroves' bioaccumulation and their ability to intercept pollutants. The BSAFs of PCBs in mangrove tissues were negatively correlated with the PCB congener's octanol-water partition coefficients (KOW, R = 0.58, n = 31, p < 0.001), suggesting that lower chlorinated CB congeners are more bioaccumulative in mangroves. In order to better understanding the fate of these organochlorine compounds, the cycling (including the standing accumulation, the annual absorption, the annual net retention, the annual return, and the turnover period) of OCPs and PCBs in the Mangrove Reserves were estimated, and the results indicated that mangroves are playing important roles in retaining OCPs and PCBs.

Persistent reductions in the bioavailability of PCBs at a tidally inundated Phragmites australis marsh amended with activated carbon.

In situ amendment of sediments with highly sorbent materials like activated carbon (AC) is an increasingly viable strategy to reduce the bioavailability of persistent, sediment-associated contaminants to benthic communities. Because in situ sediment remediation is an emerging strategy, much remains to be learned about the field conditions under which amendments can be effective, the resilience of amendment materials toward extreme weather conditions, and the optimal design of engineered applications. We report the results of a multiyear, pilot-scale field investigation designed to measure the persistence and efficacy of AC amendments to reduce the bioavailability of polychlorinated biphenyls (PCBs) in an intertidal Phragmites marsh. The amendments tested were granular AC (GAC), GAC with a layer of sand, and a pelletized fine AC. Key metrics presented include vertically resolved black carbon concentrations in sediment and PCB concentrations in sediment, porewater, and several invertebrate species. The results demonstrate that all 3 amendments withstood Hurricane Sandy and remained in place for the duration of the study, successfully reducing porewater PCB concentrations by 34 to 97%. Reductions in invertebrate bioaccumulation were observed in all amendment scenarios, with pelletized fine AC producing the most pronounced effect. The present findings support the use of engineered AC amendments in intertidal marshes and can be used to inform amendment design, delivery, and monitoring at other contaminated sediment sites. Environ Toxicol Chem 2018;37:2496-2505. © 2018 SETAC.

PAHs, OCPs and PCBs in sediments from three catchments in Durban, South Africa

Polycyclic aromatic hydrocarbons (PAHs), organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were analysed from sediment samples collected in 2012 from rivers, surface runoff canals and estuaries in three highly urbanised catchments in durban, KwaZulu-Natal, South Africa. PAHs were ubiquitous, at concentrations between 36–6 800 ng g−1 dry mass (dm). Congener ratio diagnosis suggests the PAHs were derived predominantly from pyrogenic sources. Four OCPs and/or their metabolites were detected at varying frequencies and concentrations. Of these, dichlorodiphenyltrichloroethane (ddT) and metabolites were most frequently detected and were at a high concentration in sediment in some systems. Toxaphene was detected at a high concentration at some sites. The total PCB concentration varied widely, from below the method detection limit to 110 ng g−1 (dm). Based on the comparison of chemical concentrations to international sediment quality guidelines, PAH, OCP and PCB concentrations in most sediment samples posed a low risk to sediment-dwelling organisms. However, in some instances the risk was moderate or high. It is recommended that these compounds be monitored more frequently and comprehensively in aquatic ecosystems to better understand the ecological and human health implications.

Polychlorinated biphenyl (PCB) contamination in Galveston Bay, Texas: Comparing concentrations and profiles in sediments, passive samplers, and fish.

The industrialized portion of the Houston Ship Channel (HSC) is heavily contaminated with anthropogenic contaminants, most prominent of which are the polychlorinated biphenyls (PCBs). This contamination has driven adaptive evolution in a keystone species for Galveston Bay, the Gulf killifish (Fundulus grandis). We investigated the geographical extent of PCB impacts by sampling 12 sites, ranging from the heavily industrialized upper portion of the HSC to Galveston Island. At each site, PCB concentrations and profiles were determined in three environmental compartments: sediment, water (polyethylene passive samplers), and fish tissue (resident Gulf killifish). We observed a steep gradient of PCB contamination, ranging from 4.00 to 100,000 ng/g organic carbon in sediment, 290-110,000 ng/g lipid in fish, and 4.5-2300 ng/g polyethylene in passive samplers. The PCB congener profiles in Gulf killifish at the most heavily contaminated sites were shifted toward the higher chlorinated PCBs and were highly similar to the sediment contamination profiles. In addition, while magnitude of total PCB concentrations in sediment and total fish contamination levels were highly correlated between sites, the relative PCB congener profiles in fish and passive samplers were more alike. This strong correlation, along with a lack of dependency of biota-sediment accumulation factors with total contamination rates, confirm the likely non-migratory nature of Gulf killifish and suggest their contamination levels are a good site-specific indicator of contamination in the Galveston Bay area. The spatial gradient of PCB contamination in Galveston Bay was evident in all three matrices studied and was observed effectively using Gulf killifish contamination as an environmentally relevant bioindicator of localized contamination in this environment.

Assessing measurable adverse changes to benthic invertebrate communities based on site-specific sediment toxicity testing and community data at the Anniston, Alabama PCB site

ABSTRACTLaboratory toxicity tests were conducted for polychlorinated biphenyl (PCB)-containing sediment from Choccolocco Creek at the Anniston PCB Site. The objective of this investigation was to develop a site-specific PCB concentration–response relationship for invertebrate test organisms. Test results from reference locations were used to develop background-adjusted 10% (EC10*) and 20% (EC20*) effect concentrations for a range of survival, growth, and reproduction endpoints. The EC20* values ranged from 4.43 to 114 milligrams of PCBs per kilogram (mg/kg) of sediment on a dry weight basis for reproductive endpoints, 28 to 67.7 mg/kg sediment for growth, and 123 to 165 mg/kg sediment for survival. The aggregate EC20* response range for endpoints that demonstrated good test performance with reasonable ranges in control variability (<20%) and reference sample responses was 14.3 to 165 mg/kg. The PCB concentrations in sediments for a majority of the Site rarely exceed even the lowest of these thresholds. Given the protective process used to develop these thresholds, there is a high level of confidence that benthic communities are not impacted. This finding is supported by direct measurements of the benthic communities that have been living and reproducing on the Site.

PCB dechlorination hotspots and reductive dehalogenase genes in sediments from a contaminated wastewater lagoon

Polychlorinated biphenyls (PCBs) are a class of persistent organic pollutants that are distributed worldwide. Although industrial PCB production has stopped, legacy contamination can be traced to several different commercial mixtures (e.g., Aroclors in the USA). Despite their persistence, PCBs are subject to naturally occurring biodegradation processes, although the microbes and enzymes involved are poorly understood. The biodegradation potential of PCB-contaminated sediments in a wastewater lagoon located in Virginia (USA) was studied. Total PCB concentrations in sediments ranged from 6.34 to 12,700mg/kg. PCB congener profiles in sediment sample were similar to Aroclor 1248; however, PCB congener profiles at several locations showed evidence of dechlorination. The sediment microbial community structure varied among samples but was dominated by Proteobacteria and Firmicutes. The relative abundance of putative dechlorinating Chloroflexi (including Dehalococcoides sp.) was 0.01-0.19% among the sediment samples, with Dehalococcoides sp. representing 0.6-14.8% of this group. Other possible PCB dechlorinators present included the Clostridia and the Geobacteraceae. A PCR survey for potential PCB reductive dehalogenase genes (RDases) yielded 11 sequences related to RDase genes in PCB-respiring Dehalococcoides mccartyi strain CG5 and PCB-dechlorinating D. mccartyi strain CBDB1. This is the first study to retrieve potential PCB RDase genes from unenriched PCB-contaminated sediments.

Spatial variation of PAHs and PCBs in coastal air, seawater, and sediments in a heavily industrialized region

Concurrent coastal seawater (n=22), sediment (n=22), and atmospheric samples (n=10) were collected in the Aliaga industrial region, Turkey, to explore the spatial variation, sources, and air-seawater exchange of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Seawater Σ16PAH concentrations (particle+dissolved) ranged between 5107 and 294,624pgL-1, while Σ41PCB concentrations were in the range of 880-50,829pgL-1. Levels in sediments were highly variable ranging between 35.5-49,682 and 2.7-2450μgkg-1 in dry weight for Σ16PAHs and Σ41PCBs, respectively. Atmospheric concentrations varied between 1791-274,974 and 104-20,083pgm-3 for Σ16PAHs and Σ41PCBs, respectively. Sediment organic matter (OM) content and levels of Σ16PAHs and Σ41PCBs correlated weakly (r 2=0.19-0.23, p<0.05) suggesting that the spatial variations of PAHs and PCBs were mainly affected by local sources rather than their sorption to OM. The geographical distribution of PAH and PCB concentrations in air, seawater, and sediment and factor analysis on the sediment levels pointed out that the major sources in the region are steel plants, petroleum refinery, petrochemical complex, ship breaking, loading/unloading activities at the ports, vehicular emissions, and fossil fuel combustion emissions. The direction of the air-seawater exchange was also explored by estimating seawater fugacity fractions of PAHs and PCBs. For PAHs, the number of cases implying deposition (43.0%) and volatilization (39.5%) was similar, while for PCBs, the number of cases implying volatilization (60.4%) was much higher compared to deposition (21.6%). Fugacity fractions were generally <0.36 (deposition) at the sites close to industrial and ship breaking activities where the highest seawater and sediment levels were measured, implying that atmospheric deposition is an important mechanism affecting seawater and sediment PAH and PCB levels.

Impacts of channel morphology on residues and ecological risks of polychlorinated biphenyls in water and sediment in Chahe River

The impacts of channel morphology on the residues and ecological risks of 14 polychlorinated biphenyl (PCB) congeners in water and sediment were investigated in summer (July) and autumn (September) in the Chahe River, in Nanjing, China. The residual concentrations of tri-chlorobiphenyls (tri-CBs, PCB 18) and tetra-CBs (PCB 52) in water were significantly higher than those of penta-CBs to deca-CBs, and the average residual concentration of ∑PCBs (sum of 14 PCB congeners) in summer was about six times higher than in autumn. However, the residues in sediment did not change significantly. Redundancy analysis (RDA) indicated that channel morphology and the corresponding environmental indices had significant impacts on PCB residues and their composition profiles in water and sediment. The overflow weir and lake-type watercourse may remarkably reduce the residual concentration and ecological risks of PCBs in water. The highest reduction percentages of the residual concentration and ecological risks of ∑PCBs induced by an overflow weir were 78% and 67%, respectively, and those induced by a lake-type watercourse were 36% and 70%, respectively. The watercourses with different channel morphologies were ranked by residual ∑PCBs concentrations in the following descending order: the natural ecological watercourse, vertical concrete watercourse, and vegetation-type riprap watercourse. However, they were ranked by residual ∑PCBs concentrations in sediment in the following descending order: the vertical concrete watercourse, vegetation-type riprap watercourse, and natural ecological watercourse.

CHARACTERISTICS OF MARINE ENVIRONMENTAL GEOCHEMISTRY FROM HA TINH TO QUANG NAM (60-100M WATER DEPTH)

CHARACTERISTICS OF MARINE ENVIRONMENTAL GEOCHEMISTRY FROM HA TINH TO QUANG NAM (60-100M WATER DEPTH)

Spatial Distribution Characteristics and Risk Assessment of Polychlorinated Biphenyls (PCBs) in Sediments and Soils from the Dishui Lake and Its River System

In order to investigate the pollution levels of PCBs in urban artificial lake, fourteen PCB congeners in sediments and soils of Dishui Lake and its river system were quantified by GC/MS, and then the distributions, sources and ecological risk of PCBs were discussed. The results showed that the concentrations of ∑14 PCBs in sediments and soils ranged from 0.65-16.41 ng·g^-1 (dry weight, dw) and 0.47-1.27 ng·g^-1, respectively, which were at a low level in general. Higher concentrations of PCBs were found in surface sediments from the river system of Dishui Lake than those in surface and core sediments from Dishui Lake, which indicated that the sediments in Dishui Lake would be polluted by the river system in the process of diversion. The concentrations of PCBs in core sediments decreased with depth, which showed that the sediments of Dishui Lake had been polluted by PCBs since its completion. In all samples, Tetra-CBs and Penta-CBs accounted for 20.65% and 67.12% of ∑14 PCBs, respectively, and PCB105, PCB118 and PCB77 were the dominant compounds. The results of source apportionment by principal component analysis (PCA) indicated that PCBs in sediments and soils from Dishui Lake and its river system were influenced by the historical cumulative emissions of 2#, 1# PCBs used in China and municipal solid waste incineration and combustion sources. The toxic equivalents (TEQs) of 12 (DL-PCBs) ranged from 0.01-79.40 pg·g^-1, and the TEQs in 7 samples of surface sediments from Dishui Lake and its river system were beyond the interim sediments quality guidelines (ISQGs) suggested by USEPA, which would result in potential eco-toxicological risks for aquatic organisms.