Occurrence,distribution and possible sources of organochlorine pesticides in peri-urban vegetable soils of Changchun,Northeast China

The characterizations of residue levels and sources of organochlorine pesticides (OCPs) in soils are necessary to evaluate the potential pollution and risks of OCPs to the ecosystems and human health. A total of 51 surface soil samples were collected from peri-urban vegetable fields of Changchun and 13 OCPs were analyzed to learn the composition, spatial distribution and sources. The concentrations were in the ranges of 0.94–107.8 ng g^?1 for DDTs, 0.89–98.3 ng g^?1 for HCHs, 0.22–18.20 ng g^?1 for Chlordanes, nd–4.49 ng g^?1 for aldrin and nd–9.66 ng g^?1 for dieldrin, respectively. The total OCPs concentrations ranged from 2.44 to 177.1 ng g^?1 and the higher residues were mainly distributed in northeast and southwest sites, as well as sites along the Yitong River. According to the concentrations and detection frequencies, DDTs and HCHs were the most dominant compounds. Compositional analysis and principal component analysis suggested that DDT, HCH and chlordane in most soil samples derived from historical application except the slight fresh introduction at some locations. There exist a variety of OCPs residues in peri-urban vegetable soils of Changchun, but it is still safe and suitable for agricultural production for the most part, and some specific locations with high OCPs residues ought to be a cause for concern.     

南亚热带典型地区农业土壤中多环芳烃和有机氯农药研究

参考美国EPA标准方法对南亚热带潮汕地区农业土壤中持久性有机污染物多环芳烃（PAHs）和有机氯农药（OCPs）进行分析,并对其分布和来源进行研究,最后探讨了不同种植方式下污染物的污染特征。结果表明：该区农业土壤中PAHs含量范围从22．1ng／g到1256．9ng／g,与其它地区的污染程度和一些土壤环境质量标准相比,该区处于中等污染水平。高温裂解是土壤PAHs的主要来源。OCPs在被禁止20a后在土壤中仍有残留,残留水平从4．6ng／g到1021．5ng／g,其中HCHs和DDTs的残留未超过国家土壤环境质量标准。早期使用残留是其主要污染源,但新近仍有DDT和硫丹的输入。PAHs和OCPs的污染主要集中在土壤表层和亚表层,且随着深度的加深,污染逐渐减少,但40cm以下,污染变化很小。菜地土壤PAHs污染水平低于稻田土壤,而OCPs污染水平高于稻田土壤。     

Distribution characteristics,sources, and ecological risk assessment of polycyclic aromatic hydrocarbons in sediments from Haizhou Bay,China

Sixteen USEPA priority polycyclic aromatic hydrocarbons (PAHs) were analyzed by gas chromatography–mass spectrometry. Twenty samples were collected from the surface sediments of Haizhou Bay in this survey. This research aimed to identify the PAHs' contamination level, composition pattern, pollution sources, and assess the ecological risk of PAHs. The results showed that the sum of PAH concentrations ranged from 116.6 ng g^?1 to 2414.9 ng g^?1 (mean: 662.42 ng g^?1), which is higher than the reported values for different wetlands worldwide. Three- and four-ring PAHs (accounts for more than 70% of the total PAH content) were predominant in the wetland sediment. The PAHs source distribution in the surface sediments were determined using diagnostic ratio and PCA/MLR. Consequently, multiple PAHs sources were found. Of the total PAH, 79.25% was derived from vehicular emission, 20.75% from coal combustion. The effect range low/effect range median (ERL/ERM) values indicated a low toxicity risk level. However, the fluoranthene concentrations exceeded the ERL level, and even the ERM level, in some stations. The mean effects range–median quotient (M-ERM-Q) suggests a low ecological risk for the PAHs in the sediments.     

Residues of Aliphatic and Polycyclic Aromatic Hydrocarbons in Some Fish Species of Lake Temsah,Ismailia, Egypt: An Analytical Search for Hydrocarbon Sources and Exposure Bioindicators

Residues of aliphatic and polycyclic aromatic hydrocarbons (PAHs) were monitored in some fish species collected from Temsah Lake, near Ismailia, Egypt. Fish were selected to represent different feeding habits and ecological niches in the lake's ecosystem. Fish samples were extracted using organic solvents, and residues of aliphatic and PAHs were separated using column chromatography and detected using gas liquid chromatography. Fish species were Clupea sirm, Mugil sehli, Mugil capito, Morone labrax, and Sciasna sp. Clupea sirm, a surface feeder fish had the highest concentration of aliphatic hydrocarbons, 320 ± 54 ng g^?1, while Morone labrax, a predatory fish that live in the water column, had the highest concentration of PAHs, 315.87 ± 46 ng g^?1. Even-number aliphatic hydrocarbons were more frequently detected in all fish species in comparison to odd-number aliphatic hydrocarbons, suggesting a petrogenic origin of these compounds. Meanwhile, the pattern of PAHs detected in the present study suggested that they originate from atmospheric deposition rather than land-based runoff. Morone labrax fish and Clupea sirm fish were the most suitable candidate bioindicators of exposure to aliphatic hydrocarbons and PAHs through fish consumption of the five fish species examined in this study.     

Pollution,sources, and ecological-health risks of polycyclic aromatic hydrocarbons in coastal waters along coastline of China

Abstract

This study investigated the distribution, sources, and potential risks of polycyclic aromatic hydrocarbons (PAHs) in coastal waters along over 18,000?km of coastline in China. Concentrations of PAHs in coastal waters ranged from 141.99 to 717.72?ng/L. Approximately 84.38% of sampling sites were determined at moderate PAH pollution level. PAHs in coastal waters at most of sampling sites mainly originated from combustion based on characteristic ratios of PAHs. Ecological risks posed by PAHs in coastal waters were evaluated as high level at 59.38% of sampling sites and moderate level at 40.63% of sampling sites although toxic equivalent quotients of PAHs only ranged from 2.86 to 126.52?ng/L benzo[a]pyrene that was not detected at all sampling sites. Maximal cancer risk/hazard quotient of total PAHs in coastal waters for adults and children reached 6.34?×?10^?4/5.85?×?10^?2 and 2.25?×?10^?3/7.72?×?10^?2, respectively. PAHs exerted high cancer risks for children at 31.25% of sampling sites. Health risks posed by PAHs in coastal waters of this study were higher than those of Japan, Belgium, Greece, Italy, Spain, USA, and Australia, but much lower than those of Singapore, Iran, Brazil, and Egypt. These findings indicate that PAH pollution has become a crucial stress affecting the sustainable development of coastal regions.     

Influence of anthropogenic activities on polycyclic aromatic hydrocarbons in sediments from mangrove wetland at Dongzhai Harbor,China: distribution,sources, probability risk,and temporal trend

Sixteen polycyclic aromatic hydrocarbons (PAHs) in 37 surface sediments and a sediment core from the Dongzhai National Nature Reserve in Hainan island of China were analysed. The total concentration of the 16 PAHs ranged from 15.7 to 464.0 ng g^?1 (mean value of 76.7 ng g^?1) in the surface sediments, and 8.6–115.9 ng g^?1 (average 39.3 ng g^?1) in the sediment core. Combustions of petroleum, biomass, coal, and grass were the major pyrogenic sources in surface sediments, and some areas had petrogenic sources (mainly petroleum spills). Results of the ecological risk assessment show little negative effect of most of the PAHs in the study area. The depositional flux of PAHs generally increased from the deeper layers toward the upper layers of the sediments. The flux rate rapidly increased after the 1980s, in contrast to that of some developed countries.     

Distribution,Sources Identification,and Ecological Risk of PAHs and PCBs in Coastal Surface Sediments from the Northern Persian Gulf

Hormozgan Province plays a vital role in fishery, petroleum, and industrial activities in southern Iran. However, no comprehensive studies on organic pollution have been performed. PCBs and PAHs were analyzed in surface sediments from areas receiving industrial (nine sites), river (one site), and urban (two sites) effluents. The sediment samples were collected in March and September 2010 (in dry and wet seasons) at the highest tidal time. The overall pollution level of PCBs ranged from 2.5 ± 0.8 to 462.0 ± 206.7 ng/g dry weight. CB153 congener dominated in most of the sediment samples. Congener profiles of PCBs showed close similarity with formulations of commercial products such as Aroclor 1260 and 1254 g. A wide range of 55.3 to 1231.6 ng/g dry weight was detected for ∑PAHs. Results of PCA and PCA-MLR tests confirmed both petrogenic and pyrogenic origins for PAH pollution. The higher means of ∑PAHs and ∑PCBs in industrial and urban wastewaters were found near the shore, evidencing the role of these wastewaters in the PAH and PCB contamination in Hormozgan sediment. The concentrations of PAHs and PCBs in detected hotspots exceed the U.S. NOAA sediment quality guidelines.     

Polycyclic aromatic hydrocarbons in traffic soil and Pinus needles of Beijing,China

Abstract

This study was conducted to examine the impact of vehicular traffic on the contamination status of urban traffic sites in Beijing with respect to polycyclic aromatic hydrocarbons (PAHs). The soil and Pinus pinea needle samples were collected at 12 sites on Three Ring Road in Beijing, China, from July 2009 to March 2010. Total PAH concentrations at traffic sites ranged from 113.86 to 2226.24 ng g^?1 with an average value of 658.71 ± 742.41 ng g^?1 in soil samples and 112.03 to 2016.80ng g^?1 with an average value of 680.29 ± 485.61 ng g^?1 in needle samples. The PAH pattern was dominated by two- and three-ring PAHs (contributing >80% to the total PAHs) at all the 12 traffic sites. Seasonal variations of PAHs compounds indicated the PAHs concentrations in autumn and winter were higher than those in spring and summer due to temperature effects. This work indicates that the low ring PAHs were the major profile at the roadside of a busy street with heavy traffic in Beijing.     

Distribution Characteristics and Risk Assessments of PAHs in Fish from Lake Taihu,China

The concentrations of PAHs in four species of fish (Common carp, Crucian carp, Bighead carp, and Topmouth culter) from Lake Taihu were tested, and the human health risks of PAHs by fish consumption were evaluated. Results showed that concentrations of PAHs in fish from Lake Taihu were 52.5–247.6 ng/g wet weight (ww), and the BaP equivalent concentrations of total PAHs (B[a]P_eq) were 0.2–0.6 ng/g ww, which were less than the screening value of 2.6 ng/g wet for human consumption. The concentration sequences of PAHs in fish from Lake Taihu from high to low were Bighead carp > Crucian carp > Common carp > Topmouth culter. The human health risk level of PAHs by fish consumption was 5.8 ± 2.5 × 10^?6, which was less than the maximum acceptable risk level of 1 × 10^?5 for human health set by the U.S. Environmental Protection Agency. The tissue residue guideline (TRG) of PAHs for protecting aquatic wildlife was 1.3 mg/kg diet ww, which was higher than the concentrations of PAHs in fish from Lake Taihu. The results indicated that fish consumption from Lake Taihu would not cause health risk or harmful effects on wildlife that consume aquatic biota.     

Ecotoxicological Risk Assessment of Polychlorinated Biphenyls (PCBs) in Bank Sediments from along the Yamuna River in Delhi,India

The River Yamuna originates from the Yamunotri glacier of the Himalayas and travels 22 km in the Delhi region. The river is used for various purposes in Delhi including drinking water supply. Twenty-eight polychlorinated biphenyls (PCBs) congeners were measured in bank sediments along the river, and their ecotoxicological risk was evaluated. Concentrations of ∑28PCBs varied from 0.20–21.16 ng g^?1 (dry wt.) with mean and median values of 6.63 ng g^?1 and 5.84 ng g^?1 (±0.69 ng g^?1), respectively. The concentration of 12 dl-PCBs concentrations varied from 0.04–2.86 ng g^?1 with a mean of 1.04 ± 0.11 ng g^?1, and their toxic equivalency ranged between <0.01–28.67 pg WHO-TEQ g^?1 with a mean of 10.77 ± 1.06 pg WHO-TEQ g^?1. CB-37, CB-44, CB-114, and CB-118 congeners were dominant among all PCBs congeners. The tri-PCBs (49%) were the main contributors to the PCB homolog followed by tetra-PCBs (35%), and penta-PCB (14%). Because there are no environmental guidelines in India for PCBs in river and marine sediments, concentrations of PCBs and their toxic equivalents were compared in a screening-level assessment with established freshwater sediment quality guidelines and found lower than those guideline values, which suggests no adverse ecotoxicological effect.     

Monitoring of level of mean concentration and toxicity equivalence (TEQ) of polychlorinated biphenyls (PCBs) in selected vegetables,beans and grains in khanewal and multan,Pakistan

Contamination of food chain by Polychlorinated biphenyls through use of pesticides, electric and industrial waste poses human health risk. In previous studies, PCB species were stated as endocrine disrupting pollutants and showed toxic health effects like cancerous and noncancerous in animals. The aim of this study was to investigate the levels of PCBs and its toxicity equivalence in food item from plant source to evaluate the health risk in Khanewal and Multan, Pakistan. Samples were collected and processed for further analysis of PCB species through GC/MS after extraction and clean up. The mean concentrations of PCBs ranged as 2.71–151.67 ng/g in beans and grains and 2.30–97.00 ng/g dry weight in vegetables and were lower than 200–3000 ng/g PCBs recommended by FDA tolerance level for all foods. The mean concentrations of two NDL-PCB species detected in all vegetables, beans and grains except S.indicum and T.aestivum were lower than maximum allowable concentration of non-dioxin like PCBs i.e. 40ngg^?1 reported by European Commission. Mean TEQ of sum of 14 PCB species ranged as 1.52–5.91 ng-WHO-TEQg^?1 in vegetables and 1.46–10.04 ng-WHO-TEQg^?1 in beans and grains. The present study concluded that the mean concentrations and mean TEQs of PCB species in most of the vegetables, beans and grains were found safe but due to higher consumption rate of some vegetables and grains, posed the moderate level of risk for human health. This study emphasizes on an implement of the strict rules regarding the use of restricted chemicals to diminish the effluence in food chains. Current research will be useful in up gradation of effective measures to reduce the poisonous contribution of PCB sources and the sustainability of terrestrial ecosystem in the country.     

Bioaccessibility-Based Risk Assessment of PAHs in Soils from Sites of Different Anthropogenic Activities in Lagos,Nigeria Using the Fed Organic Estimation Human Simulation Test Method

The aim of this study was to carry out a bioaccessibility-based risk assessment of polycyclic aromatic hydrocarbons (PAHs) in soils from sites of different anthropogenic activities in Lagos, Nigeria. Using an in vitro gastrointestinal model—Fed Organic Estimation Human Simulation Test method (FOREShT), the concentration of bioaccessible 16 priority US Environmental Protection Agency (USEPA) PAHs in soils were determined. Total concentration of 16 priority USEPA PAHs was also determined. The concentration range was 702–253,922 ng g^?1 and 92–760 ng g^?1 for total and bioaccessible PAHs, respectively. For persons involved with activities at these sites no health risks were observed, based on bioaccessibility values of PAHs. Mean daily intake of PAHs from these soils were below the oral mean daily intake threshold for PAHs in food. Also, overall estimated theoretical cancer risk (2.5 × 10^?09, 6.5 × 10^?07, 5.5 × 10^?10, 2.7 × 10^?09, 6.5 × 10^?10, 9.5 × 10^?10, 2.0 × 10^?09, and 4.1 × 10^?07 for the eight sites based on their bioaccessible concentration) for exposure to PAHs in surface soils were below the health guidelines for extreme (1 × 10^?04) and normal (1 × 10^?06) exposures.     

Concentration,Distribution, Source,and Risk Assessment of PAHs and Heavy Metals in Surface Water from the Three Gorges Reservoir,China

Fifteen polycyclic aromatic hydrocarbons (PAHs) and heavy metals (Cr, Ni, As, Cd, Pb, and Hg) were quantified in 19 surface water sites of the Three Gorges Reservoir, China. The total concentrations of 15 PAHs and six heavy metals in the 19 sample sites ranged from 130.8 ng L^?1 to 227.5 ng L^?1 and 3.2 μg L^?1 to 6.0 μg L^?1, respectively. The mean concentration of As was the highest among the six heavy metals (2.1 ± 0.3 μg L^?1), followed by Cr (0.5 ± 0.3 μg L^?1), Ni (1.3 ± 0.1 μg L^?1), Cd (0.2 ± 0.01 μg L^?1), Pb (0.07 ± 0.08 μ g L^?1) and Hg (0.05 ± 0.08 μg L^?1). The isomer ratio results suggest that PAHs at most sites were mainly from petroleum combustion, while coal and biomass combustion was the main source at sites 1, 2, 6, 7, 9, 14, and 17. Based on principal component analysis, the main source of heavy metals was anthropogenic activities and weathering of bedrocks. Depending on characteristic of RQ_(NCs) ≥ 1 and RQ_(MPCs) < 1, BaA showed higher potential ecological risk than other PAHs, therefore, all sampling site needed to be paid much more attention, included some remedial actions. Meanwhile, after assessing human health risk of heavy metal, it was unlikely to experience adverse health effects, even exposing through more pathways and six kinds of heavy metals simultaneously.     

Characterization,source apportionment,and human health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in road dust of a small island state in the Caribbean

Sixty-four and fifty-six road dust samples were collected over two seasons from various locations throughout the island of Trinidad and analyzed for the 16 priority PAHs. Total PAH concentrations ranged from 21 ng g^?1 to 4723 ng g^?1 (d.w.) for the rainy season and 36 ng g^?1 to 2428 ng g^?1 (d.w.) for the dry season. The Σ4–6 ring PAHs accounted for 88% and 63% of the 16 PAHs in road dust samples for the rainy and dry seasons, respectively. PAH diagnostic ratios, principal component analysis, and cluster analysis revealed both pyrogenic and petrogenic sources in road dust for the two seasons, with major contributions from vehicular emissions. Contributions from incomplete combustion and petroleum sources were also identified. The estimated Incremental Lifetime Cancer Risk (ILCR) associated with exposure to road dust PAHs in Trinidad for the rainy and dry seasons indicated no potential risk for both children and adults, as denoted by ILCR values lower than 10^?6.     

PAH contamination in road dust from a moderate city in North China: The significant role of traffic emission

To investigate the contamination level, distribution, possible source, and human exposure risk of polycyclic aromatic hydrocarbons (PAHs) in the urban traffic environment, 15 PAHs were measured in 34 road dust samples (particle size < 25 μm) collected from three grades of roads and park paths in Xinxiang, China. ΣPAHs concentrations ranged from 311 to 21200 ng g^?1, with a mean of 5890 ng g^?1 and decreased in the following order: main roads (7650 ng g^?1) > collector streets (7410 ng g^?1) > bypasses (2970 ng g^?1) > park paths (1570 ng g^?1), indicating that significant positive correlation existed between PAH contamination and traffic density. PAHs in all samples were dominantly composed of 4-ring PAHs, accounting for 44.8% of the total. Pyrene, fluoranthene, and chrysene were the predominant individual components and accounted for 14.7% (1.2–19.2%), 12.9% (3.3–20.3%), and 11.0% (2.5–18.6%) of ΣPAHs, respectively. The specific isomer ratios indicated that traffic emission was the dominant source of PAHs in road dust. The incremental lifetime cancer risk values showed that cancer risk from exposure to road dust–borne PAHs was acceptable for local residents in Xinxiang.     

Behaviour of selected PCBs,PAHs and γ-HCH in the Scheldt estuary,S.W. Netherlands

The behaviour of some organic micropollutants in the abiotic compartments water, particulate matter and bottom sediments of the Scheldt estuary, S.W. Netherlands, was studied between 1986 and 1989. Special attention was given to two individual PolyChlorinated Biphenyl congeners (PCB 52 and PCB 153), two Polycyclic Aromatic Hydrocarbons (PAHs) fluoranthene and benzo(a)pyrene and γ-HCH. Dissolved PCBs and γ-HCH behave conservatively during estuarine mixing. The concentration of γ-HCH in the fresh-water is extremely high in spring compared to the other seasons. Dissolved fluoranthene does not behave conservatively. The concentration of dissolved fluoranthene in the freshwater endmember shows a seasonal dependence with highest concentrations in winter and lowest in summer. Benzo(a)pyrene could hardly be detected in the dissolved phase with the methods used. PCBs and PAHs in particulate matter and sediments behave essentially conservatively as a result of the mixing of riverine particulates with high, and marine particulates with low organic micropollutant contents. Particulate fluoranthene is removed at low salinities under (nearly) anoxic conditions probably by microbial degradation. The rivers Scheldt and Rupel appear to be the major sources for the compounds studied. However, in particular the organic micropollutant contents of the sediments indicate that important emissions along the estuary were or are still present. Measurements of individual PCBs and PAHs in the <63 μm fraction of a dated sediment core from a salt marsh in the eastern part of the Scheldt estuary show that the recent input of PCBs and PAHs into the estuaryis probably 2–3 times lower than the maximum input in the mid-1960s. The PCB profile shows postdepositional congener-selective mobilization caused by advective transport. The PAH assemblage is remarkably uniform in the sediment core. The PAH ratios indicate that combustion of coal is the main source of PAHs in the Scheldt estuary.     

Effect of Electron Donor to Sulfate Ratio on Mercury Methylation in Floodplain Sediments under Saturated Flow Conditions

A column transport experiment was conducted to examine the release and methylation of Hg using Hg contaminated sediment from the floodplain of the South River near Waynesboro, Virginia. Three input solutions were sequentially introduced into the column. Input 1 was unamended South River water, Input 2 was river water amended with 100 mg L^?1 SO₄ and 3600 mg L^?1 lactate, and Input 3 was river water amended with 500 mg L^?1 SO₄ and 340 mg L^?1 lactate. During the first stage of the experiment (Input 1) the effluent Hg concentration was initially 4 µg L^?1 and peaked at 21 µg L^?1 and after 21 pore volumes stabilized at 13 µg L^?1. During the second stage, at high lactate to SO₄ ratios, elevated concentrations of acetic and propionic acids were detected, indicating that fermentative bacteria were dominant. During the third stage, at high SO₄ to lactate ratios, a decrease in SO₄ and an increase in H₂S concentrations were detected in the column effluent indicating that SO₄ reduction was occurring. Concentrations of methyl Hg (MeHg) in the effluent were variable over the duration of the experiment. During the first phase, concentrations of MeHg remained <3.3 ng L^?1. During the fermentative stage, concentrations of MeHg increased to a maximum value of 32 ng L^?1, and during the sulfate-reducing stage to a maximum value of 266 ng L^?1. When the column was deconstructed both molecular and cultural techniques indicated that sulfate reducing bacteria were most dominant near the influent port. These results indicate that the formation of MeHg in the sediment is not limited by the availability of Hg and that the bacterial community that contributes to mercury methylation can respond quickly to changes in the abundances of electron donors and acceptors.     

Elucidation of polycyclic aromatic hydrocarbon sources in the sinking particles in Lake Biwa, Japan

We examined monthly changes in polycyclic aromatic hydrocarbons (PAHs) in sediment trap samples collected from the northern basin of Lake Biwa, Japan, from September 2003 to July 2004 to elucidate the sources of PAHs in the lake. The most abundant concentrations were those of pyrene and fluoranthene, at μg g⁻¹ levels throughout the sampling period, with a strong positive relationship (r = 0.996, n = 10, P < 0.01). From the monthly changes in each PAH concentration and their ratios, we suspected two different sources: petroleum sources of lighter PAHs and combustion sources of middle to heavier PAHs. Because pyrene and fluoranthene decreased significantly with time during the sampling period (P < 0.05) and an abnormally high ratio of phenanthrene to anthracene was reported in September 2003, it appears that petroleum was accidentally spilled in September 2003. Although perylene was commonly found at μg g⁻¹ levels in the sediment, its concentration was comparable with those of the other PAHs in sediment trap samples. As perylene showed no significant relationship with other PAHs or other indicator molecules, we suspect that the source of perylene was different from those of other PAHs, and the perylene was mainly formed from its precursors after deposition.     

First report on OH-PAHs in South African Clarias gariepinus bile from an urban impacted system

The concentrations of selected hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) were determined in the bile of the African sharptooth catfish Clarias gariepinus from impoundments in the urban impacted Klip River system in Soweto, South Africa. Fish were sampled from three impoundments (Lenasia, Fleurhof, and Orlando dams) during the early high-flow season (September/October) of 2013. Biliary OH-PAHs were analysed using a high-pressure liquid chromatograph coupled to a tandem mass spectrometer (HPLC-MS/MS). Seven of the thirteen targeted metabolites were present in the fish of Soweto. The ΣOH-PAHs ranged between 0.1 and 1 876 ng ml^?1, with greatest ΣOH-PAH mean at Orlando (947 ng ml^?1) followed by Fleurhof (371 ng ml^?1). The most dominant metabolite in the sampling area was 2–,3–OH fluorene, ranging between not detected and 1 429 ng ml^?1, with the greatest mean at Orlando (709 ng ml^?1). PAH metabolites quantified in C. gariepinus most likely originated from the sediments. The hepatosomatic index of the C. gariepinus increased proportionally with the biliary OH-PAH concentrations. To the authors’ knowledge this data on biliary OH-PAH for fish is the first for South Africa.     

Dioxin-like Polychlorinated Biphenyls Contamination and Distribution in Soils from the Modern Yellow River Delta,China

The concentrations of 12 dioxin-like Polychlorinated Biphenyls (dl-PCBs) were determined from 37 soil samples collected from the modern Yellow River Delta (China) in March 2006. The PCB concentrations were determined by dual capillary GC-ECD. The total dl-PCBs concentrations were in the range of 108.7 to 2153 ng/kg with an average of 800.5 ng/kg. The toxic equivalency (TEQ) in this area varies from 2.3 × 10^{? 5} to 9.5 × 10^{? 5} ng-TEQ/kg, so the delta is slightly polluted by PCBs. PCB118, the main congener, accounted for 46.7% of the total dl-PCB. More than 60% dl-PCBs were penta-PCBs. The spatial distribution of the dl-PCBs is discussed in detail. The distribution of the PCBs suggests that water runoff is the main source of the total contaminant burden in the delta, and that atmospheric precipitation plays an important role.