Soil pollution by PAHs in urban soils: a comparison of three European cities

The purpose of this study was to determine the degree of contamination with polycyclic aromatic hydrocarbons (PAHs) in samples of urban soil from three European cities: Glasgow (UK), Torino (Italy) and Ljubljana (Slovenia). Fifteen PAHs (naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylene, indeno[1,2,3-c,d]pyrene) were measured in urban soil samples, using harmonised sampling, sample extraction and analyte quantification methods. Although the mean concentration of each PAH in urban soils of each city showed a wide range of values, high levels of contamination were only evident in Glasgow, where the sum of concentrations of 15 PAHs was in the range 1487-51,822 microg kg(-1), cf. ranges in the other two cities were about ten-fold lower (89.5-4488 microg kg(-1)). The three predominant PAHs were phenanthrene, fluoranthene and pyrene, with the sum of these compounds about 40% of the total PAH content. These data, together with some special molecular indices based on ratios of selected PAHs, suggest pyrogenic origins, especially motor vehicle exhausts, to be the major sources of PAHs in urban soils of the three cities. The largest concentrations for PAHs were often found in sites close to the historic quarters of the cities. Overall, the different climatic conditions, the organic carbon contents of soil, and the source apportionment were the dominant factors affecting accumulation of PAHs in soil.     

Polycyclic aromatic hydrocarbons study and toxic equivalency factor (TEFs) in Tehran, IRAN

Polycyclic aromatic hydrocarbons (PAHs) are toxic pollutants released by various urban combustion sources. Benzo[a]pyrene (BaP) is a representative member of the class of PAHs. Health risk assessment associated with inhalatory PAHs uptake is often estimated on the basis of the BaP concentrations in air. Atmospheric particulate PAHs concentrations were measured at five locations in Tehran, Iran. Sixteen PAHs were extracted from the airborne particles and analyzed by HPLC. Total PAHs concentrations (16 compounds) at five station Arjanteen, Enghelab, Azadi, Bahman, Haft Houz were respectively, 70.2, 96.5, 130, 79.1, 44.1 ng/m(3). The information obtain from the present study indicated that mean of human carcinogens are: benzo[a]antheracene (0.17-4.76 ng/m(3)), chrysene (1.74-3.62 ng/m(3)), benzo[b]fluoranthene (0-5.25 ng/m(3)), benzo[k]fluoranthene (0.32-1.72 ng/m(3)), benzo[a]pyrene (1.41-3.82 ng/m(3)), dibenzo[a,h]anthracene (0.33-2.13 ng/m(3)), and indeno[1,2,3-cd]pyrene (0.25-11.08 ng/m(3)). The development and the establishment of a toxicity equivalency factor (TEF) are used in the assessment of mixtures containing PAHs. The contribution of the carcinogenic potency of BaP alone is in the range of 49.6-76.3% of the total carcinogenic activity. The annual number of lung cancer cases (persons per million) among Tehran residents (population = 10 millions) attributable to these carcinogenic PAHs compounds in 2005 was estimated at 58 persons per million. In Tehran urban areas vehicular emission are the primary contributor to PAHs concentrations, with additional local contributors like industrials emissions.     

Non-occupational exposure to silica dust in vicinity of slate pencil industry, India

Biomonitoring of polycyclic aromatic hydrocarbons (PAHs) in the leaves of Calotropis gigantea R.Br. were performed at seven sites in the surrounding areas of a Thermal Power Plant (TPP), using the gas chromatography and mass spectrometry technique. The primary objective of the study was to monitor the degree of PAHs load in the nearby sites around TPP compared to distant sites. Total PAH (SigmaPAH) concentrations in the leaves ranged from 372.18 (at control site 7) to 4362.35 ng g(-1) d.w. (at highest polluted site 4). The concentration factors ranged from 2.65 to 11.72 for the sites located at 1 km to the point source and 1.0 to 7.08 for distant sites. The share of carcinogenic PAHs to the total PAHs differed with the site, ranging from 10.76% to 26.92%. The sites located closer to TPP have shown higher concentrations of medium and high molecular weight PAHs, which decreased gradually with the distance from the source. The total PAH burden at control site was dominated by the low and medium molecular weight PAHs compounds viz., naphthalene, acenaphthylene, acenaphthene, phenanthrene, fluoranthene, pyrene, chrysene, coronene., whilst at other sites medium and high PAHs viz., fluoranthene, pyrene, benzo (a) anthracene, chrysene, benzo (b) fluoranthene, benzo (e) pyrene and coronene showed the highest values. These results support the biomonitoring ability of Calotropis gigantea R.Br. leaves to monitor PAHs contamination.     

Analysis of polycyclic aromatic hydrocarbons in the atmospheric particulate: focused microwaves for a faster extraction method

In this paper, improvements obtained by using focused microwaves for extraction, in the analysis of polycyclic aromatic hydrocarbons (PAHs) adsorbed on particulate matter, are discussed. The method was tested on the following PAHs, which are considered to be among the most harmful with regard to carcinogenicity: benzo[a]anthracene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, indeno[1,2,3-cd]pyrene, dibenzo[a,h]anthracene. The extraction of PAHs and concentration of the sample can be performed in 3 h with a recovery of at least 70% and a maximum standard deviation of 4%. These steps are followed by clean-up on a SPE (solid-phase extraction) cartridge and analysis by GC-MS. Real samples collected in the urban area of Bari were analysed according to the proposed procedure.     

Levels of PAHs in the soils of Belgrade and its environs

Polycyclic aromatic hydrocarbons (PAHs) were analysed in 39 soil samples (0–10 cm upper layer) collected in Belgrade, the capital of Serbia. The sampling sites were randomly selected from urban, urban/recreational and rural areas; the samples were collected in April and December 2003 and July and October 2004. The sum of the 16 PAHs corresponding to the recreational zone (298 μg/kg) was close to the urban zone (375 μg/kg). Mean soil ΣPAH concentration from rural areas was 18 μg/kg dry weight. Comparing to values observed in the urbanized locations around the world, the overall levels of PAHs in this study are low. The PAH ratios obtained pointed to a domination of pyrogenically formed PAHs in the examined soils. The dominant PAHs in soil samples in urban zones were fluoranthene, benz[a]anthracene, phenanthrene and pyrene, mostly emitted from noncatalyst vehicles which are still in use in Serbia. The total carcinogenic potency for each sampling site was calculated. Regardless of the used carcinogenic activity factors, carcinogenic potency of 7 sites were 3–9 times higher than the reference ones indicating the increased carcinogenic burden of soils from these sites.     

公园地表土中多环芳烃的分离提取及含量分析

比较加压液体萃取法、超声波辅助萃取技术和微波辅助提取技术对公园地表土中多环芳烃的提取效率,并对目标化学成分进行分析鉴定。以超高效液相色谱-三重四极杆质谱作为分析方法,共分离检测出16种多环芳烃类化合物,分别为萘、苊、苊烯、氟、菲、蒽、荧蒽、芘、苯并[a]蒽、艹屈、苯并[b]荧蒽、苯并[k]荧蒽、苯并[a]芘、二苯并[a,h]蒽、茚并[1,2,3-cd]芘和苯并[ghi]苝。结果表明:加压液体萃取法、超声波辅助萃取技术和微波辅助提取技术均可以有效提取公园地表土中多环芳烃类成分。超高效液相色谱-质谱联用技术可以有效地分析公园地表土中多环芳烃类成分。     

Distribution and potential sources of polycyclic aromatic hydrocarbons in soils around coal-fired power plants in South Africa

The distribution and potential sources of 15 polycyclic aromatic hydrocarbons (PAHs) in soils in the vicinity of three South African coal-fired power plants were determined by gas chromatography–mass spectrometry. PAH compound ratios such as phenanthrene/phenanthrene + anthracene (Phen/Phen + Anth) were used to provide reliable estimation of emission sources. The total PAH concentration in the soils around three power plants ranged from 9.73 to 61.24 μg g^?1, a range above the Agency for Toxic Substances and Disease Registry levels of 1.0 μg g^?1 for significantly contaminated site. Calculated values of Phen/Phen + Anth ratio were 0.48?±?0.08, 0.44?±?0.05, and 0.38?+?0.04 for Matla, Lethabo, and Rooiwal, respectively. Flouranthene/fluoranthene + pyrene (Flan/Flan + Pyr) were found to be 0.49?±?0.03 for Matla, 0.44?±?0.05 for Lethabo, and 0.53?±?0.08 for Rooiwal. Such values indicate a pyrolytic source of PAHs. Higher molecular weight PAHs (five to six rings) were predominant, suggesting coal combustion sources. A good correlation existed between most of the PAHs implying that these compounds were emitted from similar sources. The carcinogenic potency B[a]P equivalent concentration (B[a] Peq) at the three power plants ranged from 3.61 to 25.25 indicating a high carcinogenic burden. The highest (B[a] Peq) was found in samples collected around Matla power station. It can therefore be concluded that the soils were contaminated with PAHs originating from coal-fired power stations.     

Sedimentary record of polycyclic aromatic hydrocarbons in a sediment core from a maar lake, Northeast China: evidence in historical atmospheric deposition

A maar lake is an excellent ecosystem to study the atmospheric deposition of pollutants, as its contaminants are primarily by atmospheric deposition. In this study, a sediment core from Sihailongwan Maar Lake, Northeast China, was collected and the historical atmospherically deposited polycyclic aromatic hydrocarbons (PAHs) were analyzed. The concentrations of TPAHs (the sum of the US EPA proposed 16 priority PAHs, excluding naphthalene and pyrene) ranged from 473.9 to 2289 ng g(-1) with a slow increasing stage in the deeper sediments and a sharp increasing stage in the upper sediments. The input rate of TPAHs, especially that of PAH(9) (the sum of fluoranthene, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd)pyrene, dibenzo(ah)anthrathene, and benzo(ghi)perylene), correlated well to the Chinese historical socioeconomic data. This indicates that sediment PAHs were mainly derived from human activities and PAH(9) can be regarded as a better indicator of the local socioeconomic development. Source identification suggested that PAHs were originated primarily from mixed sources (e.g., coal and biomass burning and petroleum combustion), except for perylene which was mostly of diagenetic origin. In addition, the down-core PAHs profile clearly illustrated that PAHs sources in Northeast China experienced a transformation from low- and moderate temperature to high-temperature combustion processes, especially after the late 1980s. Additionally, an ecological risk assessment using two redefined biological thresholds (TEQ(ERL) and TEQ(ERM)) indicated that most of the PAHs measured in the present sediment core would not cause an immediate toxic effect; only FLU and PHEN are a potential source of concern for biological impairment.     

Bioaccumulation of PAHs in the Zebra Mussel at Times Beach, Buffalo, New York

The zebra mussel, Dreissena polymorpha, was utilized in an in situ study in the Times Beach Confined Disposal Facility (CDF) located in Buffalo, New York, Mussels, placed both in the water column (upper position) and at the sediment surface (lower position), survived a 34-day exposure to the CDF. At the CDF, total polycyclic aromatic hydrocarbon (PAH) concentrations in the water column were below detection limits (<0.010 mg 1-1), mean total PAH concentrations in the sediment were 164.41 mg kg-1, and mean total PAH concentrations in mussel tissues after the 34-day exposure were 6.58 mg kg-1. PAH concentrations in mussels exposed for 34 days at the CDP were compared to a baseline PAH concentrations in mussel tissue prior to study initiation (Day 0), and mussel tissue from the reference site (Black Rock Channel Lock). There was a significant increase in total PAHs in mussel tissues over the 34 Day period at the CDF. No significant accumulation occurred at the reference site. PAHs which increased significantly in mussel tissue at the CDF were fluoranthene, pyrene, chrysene, and benzo(a)anthracene. Benzo(a)anthracene concentrations increased significantly in mussels at the upper position overall at Times Beach. Concentrations of Total PAHs, fluoranthene, pyrene, and chrysene were not related to position.     

Polycyclic aromatic hydrocarbons in surface sediments from drinking water sources of Taihu Lake, China: sources, partitioning and toxicological risk

Sources, partitioning and toxicological risk of 15 priority polycyclic aromatic hydrocarbons (PAHs) in surface sediments from drinking water sources of Taihu Lake, with an area of 2428 km(2) located in the most developed and populated area of China, were studied, and the results were compared with those in other lakes of China and the USA. Concentrations of the 15 PAHs in sediments ranged from 436.6 to 1334.9 ng g(-1) (dw). Gasoline combustion, coal combustion, diesel combustion from shipping and spillage of petroleum were apportioned to be the main sources of PAHs in this area by principal component analysis, which contributed 35.19%, 26.43%, 25.41% and 12.97% to the PAH sources estimated by further multiple linear regression. Levels of PAHs in sediments were negatively correlated with contents of clay and fine silt (<16 μm), while positively with contents of medium silt, coarse silt and sand (>16 μm). Humin with size larger than 16 μm contained the largest part of the burden of PAHs in sediments, but the specific partitioning domain (bound humic acid, lipid or insoluble residue) depended on properties of organic matter reflected by optical absorbance at 465 and 665 nm. Total toxic benzo[a]pyrene equivalent (TEQ(carc)) of the carcinogenic PAHs in sediments varied from 31.8 to 209.3 ngTEQ(carc) g(-1). Benzo[a]pyrene and dibenzo[a,h]anthracene contributed 45.36 and 25.31% to total TEQ(carc), posing high toxicological risk to this area.     

Determination of Polycyclic Aromatic Hydrocarbons in Rougan, a Traditional Chinese Barbecued Food, by Capillary Gas Chromatography

Several polycyclic aromatic hydrocarbons (PAHs), including those which are carcinogenic, have been detected in rougan, a traditional Chinese barbecued pork dish. The food samples were cleaned up by caustic digestion, solvent extraction, liquid-liquid partition, and column chromatography. The determination was carried out using capillary gas-chromatography with a flame ionization detector. A 25-m HP-1 capillary column was used. Fluorene, phenanthrene, anthracene, benzo[a]anthracene, chrysene and benzo[k]fluoranthene were detected in three of the five samples within the range of 3-17 ng/g. Fluoranthene and pyrene were detected in only two of the samples at similar levels. Two potent carcinogenic compounds, benzo[a]pyrene and benzo[b,j,k]fluoranthene, were not detected in any of the samples. No detectable PAHs have been found in meat cooked without the direct contact of food with flame and smoke. In barbecuing over an open charcoal fire, animal fat and juices dripping onto the open fire probably enhanced the formation of PAHs.     

Occurrence of dissolved PAHs in the Jinsha River (Panzhihua)--upper reaches of the Yangtze River,Southwest China

16 priority polycyclic aromatic hydrocarbons (PAHs) were determined in water samples from the Jinsha River (Panzhihua part), Southwest China. Total dissolved PAH concentrations varied from 21.89 microg l(-1) to 382.8 microg l(-1). It was found that the concentration of PAHs decreased along the flow direction due to the higher density distribution of coal chemical industry in the upstream of our study rivers. The pollution levels in our study area are significantly higher than previously reported values in other waters both in China and other countries. The predominance of benzo[k]fluoranthene and indeno[1,2,3-cd]pyrene was clearly observed in all water samples. On average these two compounds accounted for 98.3% of the total dissolved PAH concentration in water. The results showed the positive correlations among total dissolved PAHs, benzo[k]fluoranthene and indeno[1,2,3-cd]pyrene, which suggested that these two predominant PAHs have similar source and environmental behaviors in our study area. When compared with the survey results of organic micropollutants two decades ago, it was found that hydrocarbon pollution both predominated and even increased with the development of coal chemical industry in this area during the past 20 years. The results therefore provide important information on the current contamination status of a key industrial city in China, and points to the need for urgent action to investigate the relationship between the PAH composition and concentration in water from the Jinsha River and the wastewater discharge from coal chemical industry, and to identify the source, transport pathway and fate of PAHs in the area. It should then be necessary to adopt appropriate and instant measures to control the pollution around this area.     

Particle-bound polycyclic aromatic hydrocarbons in an urban, industrial and rural area in the western Mediterranean

Particle-bound PAHs were measured at three sites in southeastern Spain (an urban background location, a suburban-industrial site in the vicinity of two cement plants and a rural area) in order to investigate the influence of the type of location on PAH concentrations. A clear influence of cement production on particulate PAH levels could not be established since for the urban background and suburban-industrial sites the average concentrations of total PAHs in the PM2.5 fraction were very similar (1.085 and 1.151 ng m(-3), respectively), with benzo[b+k]fluoranthene and chrysene as the predominant compounds. Diagnostic ratios, used to identify PAH emission sources, pointed to traffic as the main source of particulate PAH at both locations. As expected, PAH levels at the rural site were significantly lower (0.408 ng m(-3) in the PM10 fraction) due to increasing distance from the emission sources. PAH seasonal variations at the urban background and suburban-industrial sites were the same as reported in many previous studies. Average winter to summer ratios for total PAHs were 4.4 and 4.9 for the urban background and industrial sites, in that order. This seasonal cycle could be partially explained by the higher temperature and solar radiation during summer enhancing PAH evaporation from the particulate phase and PAH photochemical degradation, respectively. The study of PAH distribution between the fine and coarse fraction at the urban site revealed that on average around 80% of total PAHs were associated with fine particles.     

Distribution and source of polycyclic aromatic hydrocarbons (PAHs) in the surface soil along main transportation routes in Jiaxing City, China

Polycyclic aromatic hydrocarbons (16 EPA-PAHs) in urban surface soil from Jiaxing City were determined using HPLC. The total concentration of 16 EPA-PAHs was detected from 18.73 to 441.34 pg/g. Individual PAH occupation analysis demonstrates that four-ring PAHs comprise as much as 44.16% and were prevalent in the composition of PAH pollutants. The other components were two-ring PAHs (7.36%), three-ring PAHs (17.28%), five-ring PAHs (16.16%), and six-ring PAHs (15.04%). Source analysis on the characteristic ratios of anthracene(Ane)/[Ane+phenanthrene(Phe)], fluoranthene(Fla)/[Fla+pyrene(Pyr)], and benzo[a]pyrene(Bap)/benzo[g,h,i]perylene(Bgp) reveals that PAH pollutants originated mainly from coal combustion, but vehicular emission as a source was not negligible. All PAHs discussed in the paper have similar source in most sampling sites. The spatial distributions of pollution sources were closely related to geographic location, geographic condition, and living habit of indigenes. A linear relationship between 2-3-ring PAHs, 4-6-ring PAHs, SOM, and ∑PAHs were investigated and significant correlativity were expatiated lastly. It revealed that coefficient between 2-3-ring PAHs and ∑PAHs is 0.56, between 4-6-ring PAHs and ∑PAHs is 0.99, between SOM and ∑PAHs is 0.82.     

Polycyclic aromatic hydrocarbon (PAH) concentration and composition determined in farmed blue mussels (Mytilus edulis) in a sea loch pre- and post-closure of an aluminium smelter

Concentrations of polycyclic aromatic hydrocarbons (2- to 6-ring parent and branched PAH) from an actively producing commercial shellfish farm in Loch Leven, Scotland, were found in excess of 4000 ng g(-1) wet weight tissue. These concentrations were considerably greater than had been recorded from mussels sampled elsewhere around the Scottish mainland. The PAH composition of the mussels from Loch Leven was dominated by the 5-ring, parent compounds; benzo[b]fluoranthene was the dominant compound. This data was consistent with the source being a discharge from an aluminium smelter. The individual compounds benz[a]anthracene, benzo[a]pyrene and dibenz[a,h]anthracene returned values of 304 ng g(-1), 446 ng g(-1) and 39 ng g(-1) respectively; these were well above the 15 ng g(-1) pragmatic guideline limit. Over the two year monitoring period, the concentrations of these compounds in mussels from Loch Etive, a reference location, ranged between 'not detected' and 4 ng g(-1)(for benz[a]anthracene). Mussels were transferred from a clean location to Loch Leven which demonstrated that the rate of uptake of PAH was rapid. Following closure of the aluminium smelter, the PAH concentrations in mussels decreased. Differences between the two sites within Loch Leven were noted with the longer-term impact remaining greater for the mussels closer to the original point discharge.     

Vertical distribution of polycyclic aromatic hydrocarbons (PAHs) in Hunpu wastewater-irrigated area in northeast China under different land use patterns

The concentrations of polycyclic aromatic hydrocarbons (PAHs) were determined in groundwater and soil profiles from upland field and paddy field in the Hunpu wastewater-irrigated area of northeast China. In the study area, the peak concentrations of total PAHs were within or just below the topsoil, and the contents decline with depth at various trend verified by the Spearman's rank correlation test. The total PAH concentrations in upland soil layers ranged from 46.8 to 2,373.0 microg/kg (dry wt.), while the concentrations in paddy soil layers ranged from 23.1 to 1,179.1 microg/kg (dry wt.). The 16 priority PAHs were all detected in the analyzed soil samples, and naphthalene (Nap), phenanthrene (Phe), fluoranthene (Fla), chrysene (Chr), and benzo[a]pyrene (Bap) were selected for further study in terms of their vertical distributions. The concentrations of both total and individual PAHs in upland soil were generally higher than those in the corresponding layers of paddy soil. The concentrations of total and individual PAH were notably different between the corresponding horizons in upland and paddy soil were probably attribute to the different sources and properties of the PAHs and soil; different methods of soil tillage and plant growing. Special PAH compound ratios, such as phenanthrene/anthracene, fluoranthene/pyrene, LMW/HMW, and parent PAH ratios (Ant/178, Fla/202, BaA/228, and Ilp/276) were used to identify the source of soil PAHs. The data suggests that the possible sources of PAHs in the Hunpu wastewater-irrigation area are the incomplete combustion of coal, petroleum and crude oil, automobile exhausts. These sources lead to pollution of the soil and groundwater by wet/dry deposition and vertical downward migration.     

Persistent organic pollutants in European background air: derivation of temporal and latitudinal trends

Data are presented for polynuclear aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), polybrominated diphenyls ethers (PBDEs) and selected organochlorine compounds (OCs) in passive air samplers (PAS) along a rural/remote latitudinal transect from southern UK to northern Norway during 2002-2004. This study is part of an ongoing campaign, using semi-permeable membrane devices (SPMDs) as PAS over two year intervals since 1994. Data for PCBs, selected OCs and PBDEs are compared with that from previous campaigns. Absolute sequestered amounts of selected PCB congeners have decreased in a first order fashion between 1994-2004, with an average atmospheric clearance rate of 4.1 +/- 0.6 years and continue to fractionate with latitude. HCB has also declined between 1998-2004, with a clearance rate of 6 +/- 2.4 years. Data on DDT and its breakdown products indicate little fresh release in Europe. Comparison of PBDEs in 2000-02 and 2002-04 indicates site differences, generally with increases at UK sites and decreases in Norway. BDE-28, 47 and 49 decreased with increasing latitude (p < 0.04), while the other congeners did not show any significant latitudinal dependence. Transect data are presented for PAHs the first time. Three- and 4-ringed compounds dominated the mixture present in the SPMD. The PAH composition of the SPMDs at site 3 was compared to the average composition taken by active sampling at the same site. SPMD performance for sampling PAHs leaves many uncertainties, but they can be successfully used to semiquantitatively detect PAHs in the atmosphere. Fluorene and phenanthrene increased with latitude (p > 0.05), while 1-methylphenanthere, fluoranthene, benzo[b]fluoranthene and indeno[123-cd]pyrene decreased. Results are discussed in terms of sources, long-range atmospheric transport, global fractionation and clearance processes.     

Toxic equivalency factors for PAH and their applicability in shellfish pollution monitoring studies

Fish and shellfish are exposed to a wide range of polycyclic aromatic hydrocarbons (PAH) following oil spills at sea, and can become contaminated as a result. Finfish have a more effective mixed-function oxidase enzyme system than shellfish, and are therefore able to metabolise and excrete PAH more effectively than the invertebrates. Thus, contamination by high-molecular weight PAH, including those with carcinogenic potential and so of concern with regard to human consumers, is therefore usually observed in shellfish, and particularly in bivalve molluscs. Oil spills are not the sole source of PAH, however, as parent compounds are also generated by a wide range of combustion processes. In this paper, consideration is given to monitoring data gathered following recent oil spills (both of crude oil and diesel fuel), alongside data from other studies. These include studies conducted around a former gasworks site and downstream of an aluminium smelter in the UK, and from mussel monitoring studies undertaken in the UK and the USA (including the Exxon Valdez oil spill and the National Status and Trends programme), and in other countries in Europe. For comparative purposes the PAH concentrations are summed and also expressed as benzo[a]pyrene equivalents, their relative concentrations being weighted in relation to the carcinogenic potential of individual PAH compounds using toxic equivalency factors (TEF). Our aim was to assess the utility of this approach in fishery resource monitoring and control following oil spills. Certainly this approach seems useful from the data assessed in this study. and the relative ranking of the various studies seems to reflect the relative degree of concern for human consumers due to the differing contamination sources. As a simple tool for control purposes it is equally applicable to PAH derived from oil spills, and from industrial and combustion sources.     

广东省南海市主干道气溶胶中多环芳烃(PAHs)的研究

气溶胶采样点位于广东省南海市桂江路边缘及两侧 ,采集时间为 2 4 h,连续采集三天。使用仪器为国产大体积采样器。同时在公园内设点采样 ,以作背景研究。样品经超声波抽提和层析柱分离得到正构烷烃、芳烃 (AHs)和极性组分等三种有机组分。对 PAHs进行 GC MS分析 ,气溶胶中具有较高含量的芴、菲、蒽、荧蒽、芘、苯并 [a]蒽、、苯并 [b]荧蒽、苯并 [k]荧蒽、苯并 [a]芘、茚并 [1 ,2 ,3-cd]芘、二苯并 [a,h]蒽、苯并 [g,h,i]等。通过 TSP研究认为 ,主干道的机动车排放和扬尘是气溶胶的主要来源 ,气候改变也是 TSP变化的另一重要因素。     

多环芳烃的健康风险评价以及暴露参数的敏感性分析

在暴露情景假设和评估模型的确定下,有必要对污染场地的风险计算结果有影响的模型参数开展敏感性分析,以便在开展土壤健康风险评估工作时,提高评估的准确性和科学性,节约修复成本。以上海市某污染场地为例,对模型参数敏感性开展敏感性分析。贡献率结果显示,经口摄入土壤和皮肤接触土壤为场地表层污染土壤的主要致癌风险暴露途径。敏感性分析结果显示,致癌风险与体重呈反向变化,当体重参数减小时,暴露风险将向不利的方向移动。当体重参数在大范围减小时,敏感程度较高。致癌风险与暴露周期、暴露频率、每日摄入土壤量、暴露皮肤表面积、皮肤表面土壤粘附系数呈同向变化,当这些参数增大时,暴露风险将向不利的方向移动;其中暴露周期和暴露频率的敏感程度中等。上海市敏感用地下苯并(a)蒽、苯并(b)荧蒽、茚并(1,2,3-c,d)芘、苯并(a)芘、二苯并(a,h)蒽风险控制值分别为0.726、0.726、0.726、0.072 6、0.072 6 mg/kg。