Spatiotemporal multimedia emission inventory for polycyclic aromatic hydrocarbons near petroleum production plants in China based on a 10′ × 10′ grid

A spatiotemporal model was developed to investigate emissions of polycyclic aromatic hydrocarbons (PAHs) in Daqing, a Chinese city with large petroleum industry plants. The model was based on land-use types determined on a 10′?×?10′ grid. A geographic information system and regression analyses were used to characterise spatial and temporal variations in PAH emissions into multiple environmental media. The simulated results were validated using previously published experimental data, and the model was found to function well. PAH emissions to the atmosphere, soil, and surface water between 1998 and 2013 were estimated. The results indicated that PAH emissions to the atmosphere increased but PAH emissions to the soil and surface water decreased over the study period. PAH emissions to the atmosphere were markedly higher in winter than in summer. PAH emissions were concentrated in urban areas and areas near petroleum production plants, indicating that PAH emissions were closely related to industrial activities. The results will support research into the migration and transformation of PAHs and human health and ecological risk assessments. The results may also be useful for developing policies for controlling PAH pollution and managing risks associated with PAHs.     

环渤海北部沿海地区表层土壤中PAHs的污染特征及风险评价

系统采集了环渤海北部沿海地区31个表层土壤样品,利用GC/MS分析了16种USEPA优控多环芳烃(PAHs)的含量和组分特征,运用主成分因子载荷法揭示了其污染来源,并初步评价了其风险水平.结果表明,沿海地区65%的土壤已被污染,最高污染样点PAHs含量达920.4ng·g-1,平均含量309.5ng·g-1,与国内外相关研究比较,处于中低等污染水平.各类燃料的不完全燃烧是该地区土壤中PAHs的主要来源,石油类挥发或泄漏对采油区土壤中PAHs的累积影响显著.     

Historical record of anthropogenic polycyclic aromatic hydrocarbons in a lake sediment from the southern Tibetan Plateau

High-altitude lake sediments can be used as natural archives to reconstruct the history of pollutants. In this work, the temporal distribution of polycyclic aromatic hydrocarbons (PAHs) was determined in a sediment core collected from the southern Tibetan Plateau (TP), which was dated by using the ²¹⁰Pb dating method and validated with the ¹³⁷Cs fallout peak. The concentrations of the anthropogenic PAHs (Σ₈PAH) in the sediment core ranged from 0.83 to 12 ng/g dw, and the fluxes of the Σ₈PAH were in the range of 2.1–27 g/cm²/year. The temporal variations in the concentration and input flux of anthropogenic PAHs were low with little variability before the 1950s, and then gradually increased from the 1950s to the 1980s, and an accelerated increase was observed after the early 1980s. The content of total organic carbon played an insignificant role in affecting the time trends of PAHs in the sediment core. Diagnostic concentration fractions of PAH components indicate PAHs in the lake sediment of the southern TP which are mainly from biomass burning and/or from long-range atmospheric transport.     

Source characterisation and mid-term spatial and temporal distribution of polycyclic aromatic hydrocarbons in molluscs along the Basque coast (northern Spain)

The variability of polycyclic aromatic hydrocarbons (PAH) measured in the soft tissues of Mediterranean mussels (Mytilus galloprovincialis) and Pacific oysters (Crassostrea gigas) are investigated. Samples were collected from estuarine waters within the Basque Country (Bay of Biscay), between 2003 and 2011. PAH bioaccumulation showed some seasonality and significant differences were observed between cold (autumn–winter) and warm (spring–summer) seasons. Sites located within the ports of Bilbao and Pasaia showed the highest PAH concentrations in molluscs, and the highest percentages of samples above the established Environmental Quality Standards and Environmental Assessment Criteria. Probably due to human activities carried out in the area, no clear trends were observed, between 2003 and 2011, for the autumn data. Since the Basque coast is an area with high population density and industrial activity, the congener profiles (which reveal the predominance of tetra-aromatics) and the diagnostic ratios identified urban/industrial combustion processes as the main PAH sources. However, natural and petrogenic sources cannot be disregarded.     

汕头经济特区土壤中优控多环芳烃的分布

运用气相色谱-质谱方法对汕头经济特区131个土样中的美国EPA优控多环芳烃(PAHs)进行定性、定量测定,讨论了PAHs的分布特征。结果表明,该区表层土壤中优控PAHs的总质量分数范围从22.1 ng/g到1256.9 ng/g之间,平均质量分数为(317.3210.2) ng/g。其分布随采样点的位置不同而有显著变化:工业区附近多环芳烃的质量分数最高,城市中心次之,郊区最低。大多数样点中?PAHs质量分数和单种PAH质量分数都呈现w(5~20 cm)> w(0~5 cm)>w(20~40 cm)>w(40~100 cm)的垂直分布规律。该区土壤PAHs以3环和4环化合物为主,单种PAH以萘、菲和苯并[b]萤蒽为主。     

固定化毛霉对工业和农田污染土壤中多环芳烃的降解和生物有效性评价

为了探讨微生物修复不同类型多环芳烃污染土壤的可行性,应用固定化毛霉对多环芳烃污染工业土壤及农田土壤进行微生物修复,用羟丙基-β-环糊精(HPCD)提取模拟评价多环芳烃的微生物可利用性,并分析多环芳烃微生物降解和生物可利用性的相关关系.焦化厂污染土壤中多环芳烃的30 d降解率为77.6%,沈抚灌区污染土壤中多环芳烃的30 d降解率为54.2%,焦化厂土壤和污灌区农田土壤中多环芳烃降解差异明显.焦化厂土壤和污灌区土壤中多环芳烃的30 d降解量和多环芳烃的环糊精可提取量具有相关性,各环数多环芳烃的环糊精可提取量变化解释了焦化厂和污灌区土壤中多环芳烃降解的差异机制,说明可用环糊精提取量预测微生物降解土壤多环芳烃的情况.     

Continuous monitoring of ambient polycyclic aromatic hydrocarbons near open‐air burning of metal scraps

Airborne concentrations of PAH in the vicinity of the source region with open‐air burning of metal scraps were measured between February, 1992 and November, 1993. The activity of open‐air burning decreased significantly since 1993 due to prohibition regulation. Both gaseous phase and particle‐bound PAH were measured at five sampling sites, which included one reference sampling site far away from the source region. Both values of gaseous and particle‐bound PAH concentrations, which were measured in the vicinity of source region, decreased clearly during the two years monitoring period. It shows that the uncontrolled open‐air burning of metal scraps was a significant emission source of airborne PAH in the study area. The profiles of various species of PAH were also compared. A large decrease in benzo(a)pyrene was observed in the source region.     

Vertical distribution and environmental significance of PAHs in soil profiles in Beijing,China

Vertical distribution of both the concentration and composition of polycyclic aromatic hydrocarbons (PAHs) in ten profiles in Beijing has been investigated. The results showed that PAH concentrations and compositions in topsoil from different sampling sites were different. PAH concentrations were much higher in topsoil of the investigated urban area, industrial region, and paddy field with wastewater irrigation than in other areas. Moreover, PAH concentrations in topsoil were much higher than those at greater depth, where the concentrations were relatively consistent in most soil profiles. The fingerprints of PAHs in the samples from topsoil (0–30 cm) in the same profiles were similar and were obviously different from those at greater depth, suggesting that PAH sources were consistent in topsoil samples and were discriminating between topsoil and deeper soils. PAHs in topsoil mainly arose from mixed sources of combustion of liquid fuel, coal, and/or wood, as well as wastewater irrigation, while those at greater depth were derived from soil genesis and the process of soil formation.     

Cytochrome P450 1A activity in liver and fixed wavelength fluorescence detection of polycyclic aromatic hydrocarbons in the bile of tongue-fish (Cynoglossus acrolepidotus, Bleeker) in relation to petroleum hydrocarbons in the eastern Gulf of Thailand.

This investigation was conducted in an area of oil spill along the east coast of Thailand to examine the relations among cytochrome P450 1A activity in liver and PAHs in the bile of the tonguefish and petroleum hydrocarbons in the sediments. PAH sediment concentrations in the reference and oil spill areas were 5.03 +/- 0.42 and 0.21 +/- 0.043 microg(-1) dry weight respectively Cytochrome activity in fish liver from oil spill area was 45.40 +/- 3.50 pmoles/ min/mg protein, almost threefold higher than that from the reference sites. Flourescense detection in bile metabolites at the oil spill area, 69.8 +/- 9.9 flourescense unit was significantly higher than that at the reference sites, 22.9 +/- 5.5 and 22.2 +/- 3.5 fluorescence unit. A strong correlation was found among cytochrome P450 1A activity in liver, PAH of bile metabolites and petroleum hydrocarbons. Both cytochrome and bile metabolites activity decreased seaward varying to the distance from the oil polluted area. We concluded that both detections in tonguefish can be regarded as a complementary biomarkers for the exposure of PAHs in tropical marine environments.     

Spatial distribution and temporal trends of polycyclic aromatic hydrocarbons (PAHs) in water and sediment from Songhua River, China

The spatial and temporal distributions of polycyclic aromatic hydrocarbons (PAHs) in the Songhua River, Harbin, China, were investigated. Seventy-seven samples, 42 water and 35 sediment samples, were collected in April and October of 2007 and January of 2008. The concentrations of total PAHs in water ranged from 163.54 to 2,746.25 ng/L with the average value of 934.62 ng/L, which were predominated by 2- and 3-ring PAHs. The concentrations of total 16 PAHs in sediment ranged from 68.25 to 654.15 ng/g dw with the average value of 234.15 ng/g dw, which were predominated by 4-, 5- and 6-ring PAHs. Statistical analysis of the PAH concentrations shown that the highest concentrations of the total PAHs were found during rainy season (October of 2007) and the lowest during snowy season (January of 2008). Ratios of specific PAH compounds, including fluoranthene/(fluoranthene + pyrene) (Flu/(Flu + Pyr)) and phenanthrene/(phenanthrene + anthracene) (An/(Ant + PhA)), were calculated to evaluate the possible sources of PAH contaminations. These ratios reflected pyrolytic inputs of PAHs in Songhua River water and a mixed pattern of pyrolytic and petrogenic inputs of PAHs in the Songhua River sediments. Ecotoxicological risk levels calculated for PAHs suggested that there were individual PAHs, which can less frequently cause biological impairment in some samples, but no samples had constituents that may frequently cause biological impairment. Total toxic benzo[a]pyrene equivalent of ΣcPAHs varied from 10.03 to 29.7 ng/g dw and from 0.36 to 1.92 ng/g dw for total toxic tetrachlorodibenzo-p-dioxin equivalent. The level of PAHs indicated a low toxicological risk to this area.     

珠江三角洲地区水体表层沉积物中多环芳烃的来源、迁移及生态风险评价

检测了珠江三角洲河流及南海近海表层沉积物中25种多环芳烃的含量．其含量范围为138-6793ng·g-1．主成分分析/多元回归分析结果表明,珠江三角洲水体沉积物中多环芳烃来源主要有石油排放,煤、木柴等低温燃烧排放,机动车尾气排放及生物成因．其相对贡献分别为石油排放占36％、煤、木柴燃烧占27％、机动车尾气占25％,自然来源占12％．珠江、东江河流沉积物中多环芳烃主要来源于区域内工业和生活废物的直接排入和机动车尾气的近距离沉降．西江沉积物中多环芳烃大气沉降是主要输入途径．南海沉积物中多环芳烃河流输入是主要途径．在多环芳烃由河流向海洋的输送过程中,茈可以作为一个有效指标示踪河流输送的多环芳烃．风险评价表明,东江及珠江部分河段沉积物可能存在着对生物的潜在危害,其它区域多环芳烃的生态风险处于较低水平．     

Einschätzung der Konzentrationsprofile polyzyklischer aromatischer Kohlenwasserstoffe (PAK) in Böden des Biosphärenreservates Spreewald

To work out background values, the information of concentration profiles of PAHs in soils of uncontaminated territories is indispensable. This investigation shows PAH concentrations of different soil samples like agricultural soils, grassland, forest and litter from the biosphere reserve in Spreewald, Germany. The mean values of the soil samples are about 460 μg Σ-PAK/kg d.m. A top value of 7.2 mg Σ-PAK/kg d.m. shows a sample of a flooded grassland area. The relation of the concentrations in the litter, forest, grassland and agricultural soil samples is about 5∶3∶2∶1. Compared to the other samples, the litter samples contain a higher amount of low molecular PAHs. Increasing distance to the former power plants Lübbenau and Vetschau (brown coal) lead to decreasing PAH contents in the soil samples of forests from 2190.9 after 4 km to 294.8 Σ-PAK/kg d.m. after 16 km. In comparison to results obtained in Nordrhein-Westfalen and Bayern, the PAH measurements indicate Spreewald to be an uncontaminated and rural area.     

Revealing the factors affecting occurrence and distribution of polycyclic aromatic hydrocarbons in water and sediments of Lake Baikal and its tributaries

The concentrations of polycyclic aromatic hydrocarbons (PAH), total carbon (TC), total organic carbon (TOC), total nitrogen (TN) and dissolved inorganic nitrogen (DIN) in water and sediments of Lake Baikal and its tributaries were measured. It was found that according to existing water and sediment quality standards limiting permissible PAH concentrations, both surface waters and sediments in Lake Baikal watershed can be considered as unpolluted with PAHs compounds. Nevertheless, the spatial distribution of PAH concentrations in lake water indicates the existence of some point PAH sources in and around the lake. These sources were natural oil seeps and communal facilities such as residential coal-fired and oil-fired boilers. It was observed that concentrations of PAHs in both water and sediments are controlled by organic matter content and organic matter mineralisation degree, as indicated by PAH-to-carbon and nitrogen-to-carbon ratios respectively. It was found that PAH/TOC and PAH/TC ratios characterise PAH loading on water and sediments respectively, whereas DIN/TOC and TN/TC ratios characterise self-purification of water and sediments respectively. It was proved that PAH/TOC and DIN/TOC ratios can be used as tracers to evaluate the PAH contributions from tributaries to Lake Baikal.     

Air pollution from aluminum smelting plants. II. the contribution from an aluminum smelting plant using the söderberg process to polycyclic aromatic hydrocarbons and mutagens in ambient air

Extracts of airborne particles collected in the surroundings of an aluminum smelting plant have been analyzed for polycyclic aromatic hydrocarbons (PAH) and tested for mutagenic activity. The results were discussed in relation to the meteorological conditions during sampling and showed that the ambient concentrations of these parameters are significantly influenced by the emissions from the smelting plant in the summer, but not in the winter. The results from the mutagenicity testing showed that the mutagenic activity of particle extracts from this area was equal to or lower than what has been reported from other urban areas in Scandinavia.

The contribution of PAH and mutagens to the concentrations of these compounds in ambient air was estimated based on parallel measurements of fluoride and from emission values of fluoride, PAH and mutagens. It was concluded that whereas the smelter emissions could account for more than 50% of the yearly average of ambient PAH, the contribution of mutagens was significantly less.     

Ökotoxikologische Bioindikation

Atmospheric heavy metals, (Pb, Cd, Cu, Zn), PAHs, and PCBs, depositions were monitored in scots pine needles during a monitoring network programme (Monitoring Programme Natural Budget Berlin and Environs) in 1991 in the city of Berlin, and the surrounding rural areas of Brandenburg (Germany). The total area of the network covered 3,000 km². The passive monitoring technique is based on the fact that the concentrations of heavy metals, PAH’s and PCB’s in the needles are closely correlated to atmospheric depositions/emissions. The objectives of the project were to characterize qualitatively and quantitatively the regional atmospheric deposition patterns of heavy metals, PAH’s and PCB’s in rural and polluted urban areas of Berlin and Brandenburg. The indication of the locations which could be characterized as heavy metals, PAH and PCB pollution sources was also targetted in this investigation. After conclusion, comparison with similar studies conducted in different parts of Germany and Europe would be possible. The regional background deposition levels showed different distribution patterns. The lead and PAH concentrations in the pine needles were closely correlated to the locations of combustion sources petrol, oil, brown coal and heavy traffic activities. The PCB and cadmium concentration levels in the pine needles represented a more ubiquitous distribution pattern.     

Monitoring von PAK-Metaboliten in Aalmuttern (Zoarces viviparus) aus der Wismar-Bucht

Background, aim, and scope Polycyclic aromatic hydrocarbons (PAH) are important environmental contaminants in the marine environment. The Baltic is known to be significantly contaminated with PAH. The eelpout (Zoarces viviparus) has been used for coastal monitoring in the Baltic. The aim of the present study was to elucidate whether the eelpout can be used to investigate PAH contamination in the Mecklenburg Bight and whether PAH sources may be revealed by the relation of the metabolites. Material and methods PAH metabolites were determined in the bile fluid of eelpout caught in spring 2008 at three sampling locations in the Wismar Bight. Two metabolites were determined by means of HPLC and fluorescence detection. In addition, bile pigments were measured photometrically. Results The concentrations of 1-hydroxypyrene in bile were significantly different at all three sampling locations under investigation. Highest concentrations were found near the city of Wismar with a mean value of 1086?ng/ml. Concentrations for individual fish ranged from <22.5 to 3317?ng/ml 1-hydroxypyrene. Concentrations of 1-hydroxyphenanthrene were lower and ranged from 2.1 to 803?ng/ml in individual samples. In fish caught next to the city of Wismar a mean value of 96?ng/ml 1-hydroxyphenanthrene was calculated. Discussion In the light of substantial anthropogenic contamination in this area caused by harbor, shipyards and shipping traffic, high values of 1-hydroxypyrene found in eelpout near the city of Wismar appear to be very plausible. Furtheron, the 1-hydroxypyrene results are in accordance to literature data. 1-Hydroxyphenantrene in eelpout bile was found in higher concentrations compared to earlier investigations. Spatial differences in the relation of the two metabolites may indicate a local source of PAH. Recommendations and perspectives PAH metabolites are useful parameters for monitoring the PAH pollution of fish like eelpout. Additional information regarding potential PAH sources can be gained from the relations of individual metabolites.     

Gehalte an polycyclischen aromatischen Kohlenwasserstoffen (PAK) in Oberböden Hamburgs

The contents of 19 polycyclic aromatic hydrocarbons (PAH) in topsoil samples from 108 sites within the territory of the federal state of Hamburg were analyzed. The investigation was performed to provide a view on background values in the metropolitan area and the influence of land use on PAH in soils. Known contaminated sites were not included in the investigation. Values in the area ranged from 0.1 to 44.3 mg/kg d.m. with a median of 3.6. 80% of the measurements were below 10 mg/kg d.m. Contents decreased strongly with a growing distance from the city’s center. The median is 4.4 mg/kg d.m. in the center, 1.3 in the rural periphery (marsh) and 0.4 mg/kg d.m. in preweichselian uplands (“geest”). PAH contaminations originate from diffuse atmospheric emissions caused by car traffic and room heating, but also by war damages which lead to widespread burnings and consequently to the widespread dispersion of remains. The contents measured are in the range of published values from other densely populated areas, although a comparatively comprehensive investigation from another region does not exist.     

Chemical contamination of soils in the New York City area following Hurricane Sandy

This paper presents a unique data set of lead, arsenic, polychlorinated biphenyl (PCB), and polycyclic aromatic hydrocarbon (PAH) concentrations in soil samples collected from the metropolitan New York City area in the aftermath of Hurricane Sandy. Initial samples were collected by citizen scientists recruited via social media, a relatively unusual approach for a sample collection project. Participants in the affected areas collected 63 usable samples from basements, gardens, roads, and beaches. Results indicate high levels of arsenic, lead, PCBs, and PAHs in an area approximately 800 feet south of the United States Environmental Protection Agency (US EPA) Superfund site at Newtown Creek. A location adjacent to the Gowanus Canal, another Superfund site, was found to have high PCB concentrations. Areas of high PAH contamination tended to be near high traffic areas or next to sites of known contamination. While contamination as a direct result of Hurricane Sandy cannot be demonstrated conclusively, the presence of high levels of contamination close to known contamination sites, evidence for co-contamination, and decrease in number of samples containing measureable amounts of semi-volatile compounds from samples collected at similar locations 9 months after the storm suggest that contaminated particles may have migrated to residential areas as a result of flooding.     

Removal of high concentrations of polycyclic aromatic hydrocarbons from contaminated soil by biodiesel

Solubilizing experiments were carried out to evaluate the ability of biodiesel to remove polycyclic aromatic hydrocarbons (PAHs) from highly contaminated manufactured gas plant (MGP) and PAHs spiked soils with hydroxypropyl-β-cyclodextrin (HPCD) and tween 80 as comparisons. Biodiesel displayed the highest solubilities of phenanthrene (420.7 mg·L^-1), pyrene (541.0 mg·L^-1), and benzo(a)pyrene (436.3 mg·L^-1). These corresponded to several fold increases relative to 10% HPCD and tween 80. Biodiesel showed a good efficiency for PAH removal from the spiked and MGP soils for both low molecular weight and high molecular weight PAHs at high concentrations. Biodiesel was the best agent for PAH removal from the spiked soils as compared with HPCD and tween 80; as over 77.9% of individual PAH were removed by biodiesel. Tween 80 also showed comparable capability with biodiesel for PAH solubilization at a concentration of 10% for the spiked soils. Biodiesel solubilized a wider range of PAHs as compared to HPCD and tween 80 for the MPG soils. At PAH concentrations of 229.6 and 996.9 mg·kg^-1, biodiesel showed obvious advantage over the 10% HPCD and tween 80, because it removed higher than 80% of total PAH. In this study, a significant difference between PAH removals from the spiked and field MGP soils was observed; PAH removals from the MGP soil by HPCD and tween 80 were much lower than those from the spiked soil. These results demonstrate that the potential for utilizing biodiesel for remediation of highly PAH-contaminated soil has been established.     

Distribution,levels, and risk assessment of polycyclic aromatic hydrocarbons in the soot of some kitchens in the Cape Coast Metropolis of Ghana

The effect of using firewood for cooking, baking, and heating in poorly ventilated kitchens on the formation of polycyclic aromatic hydrocarbons (PAH) in kitchen soot in the Cape Coast Metropolis of Ghana has been studied. The kitchens in Ghana, especially those in the rural areas, are simple clay hut structures with small doors. The kitchens have little or no openings for ventilation and, as a result, the cook is exposed directly to high doses of smoke containing different compounds including PAH. In this study, a total of 42 soot samples were collected for 6 weeks from seven kitchens and analyzed using gas chromatography with flame-ionization detection (GC/FID). The average PAH concentration in the kitchen soot samples ranged from 0.7 to 445 µg kg^?1. The unit risk of PAH associated with the dermal contact/inhalation of the kitchen soot occurred at 7.4 × 10^?3 in children and at 4.8 × 10^?5 in the adults, showing the impact. However, the high level of PAH measured in this work especially that of benzo[a]pyrene (B[a]P) may cause cancer in the women who are exposed to the smoke. The study was therefore designed to find out the level of PAH in kitchen soot and their contributions as the monitoring tools in the assessment of risks and hazards of PAH in Ghana.