南四湖上级湖表层沉积物中多环芳烃的含量及分布特征

对南四湖上级湖表层沉积物中的15种美国环保暑(US EPA)优控多环芳烃(PAHB)进行了定量分析.测定结果表明,沉积物中15种PAHs总合量范围为163.0～2983.8ng/g dry wt..相关分析表明,南四湖上级湖表层沉积物中PAHs浓度的空间分布受入湖河流影响较大,与入湖河流两岸的工农业布局和城市分布存在一定的相关性;南四湖上级湖表层沉积物中的多环芳烃主要来源于煤炭、木材及石油的不完全燃烧;目前南四湖上级湖表层沉积物样品中的PAHs含量处于低风险水平,尚未对生物造成显著的负面影响.     

中国表层水体沉积物中多环芳烃源解析及评价

采用索氏提取气相色谱-质谱法测定中国6个重点水体表层沉积物中16种多环芳烃的含量。各化合物含量范围分别为长江6.20~163 ng/g、淮河7.90~249 ng/g、海河12.1~401 ng/g、松花江5.75~152 ng/g、太湖29.1~2 810 ng/g和滇池19.1~795ng/g；16种多环芳烃的总量分别为：长江1 147 ng/g、淮河1 723 ng/g、海河2 595 ng/g、松花江793 ng/g、太湖12472 ng/g、滇池3 714 ng/g，属中等污染水平。利用特征分子比值法分析结果表明6条水体表层沉积物中PAHs均可能以燃料（包括柴油、汽油、煤、木材）燃烧以及焦化污染为主。淮河和滇池还可能存在轻微石油泄漏污染。利用沉积物质量基准法（SQGs）和沉积物质量标准法分别对6条水体表层沉积物中多环芳烃的风险评估表明严重的多环芳烃生态风险在这些水体表层沉积物中不存在，但长江、淮河、松花江、海河均可能存在一定的潜在风险，负面生物毒性效应会偶尔发生，风险主要来源于荧蒽和菲。太湖和滇池水体中存在的潜在多环芳烃风险种类较多，风险主要来源于菲、荧蒽、芘、苯并（a）蒽、苊和蒽，对水生生物毒性效应较高，有必要进行更深入细致的调查研究高风险区域底栖生物的受损状况、污染来源和途径，以制定合理的污染控制对策。     

南宁城市内河水体和表层沉积物中多环芳烃分布特征

采用改进的固相萃取、加速溶剂萃取和高效液相色谱对南宁7条城市内河的水体和表层沉积物样品中6种多环芳烃的残留状况进行了分析测定。检测结果表明,水体中多环芳烃以荧蒽为主,6种多环芳烃在水体中的总残留浓度为26.8～163 ng/L,内河水体各点位苯并[α]芘均超过我国地表水环境质量标准限值,对干流水质存在一定影响。7个点位沉积物中多环芳烃总含量为118.06～416.73μg/kg,6种多环芳烃均有检出。     

京杭大运河扬州段表层沉积物中多环芳烃的分布及风险评价

采用HPLC定量检出京杭大运河扬州段表层沉积物中16 种优控PAHs 的总量范围在505~4532.2ng/g (干重) 之间,平均值为2359.4ng/g,属中等污染水平,沉积物中的多环芳烃主要来源于煤炭、木材及石油的不完全燃烧;利用沉积物质量基准法(SQGs)对京杭大运河扬州段沉积物中多环芳烃的风险评价表明, 严重的多环芳烃生态风险在京杭大运河扬州段沉积物中不存在,负面生物毒性效应会偶尔发生, 风险主要来源于低环的多环芳烃。     

天津滨海新区黑潴河下游沉积物多环芳烃风险评价及环境基准值的比较

对黑潴河下游表层沉积物中16种多环芳烃(PAHs)的污染现状进行了调查研究。结果表明,表层沉积物中PAHs总量变化范围为41.2～129.3ng/g(平均值为83.7ng/g),PAHs的组成以5～6环PAHs组分为主。黑潴河下游沉积物中PAHs主要来源于周边地区化石燃料的高温燃烧。比较了基于不同方法建立的沉积物中PAHs环境基准值的差异,分析产生差异的原因,选择生态效应区间法对黑潴河沉积物中的PAHs进行了生态风险评价。黑潴河下游PAHs生态风险较小,属PAHs低生态风险河道。     

广州大学城珠江水域多环芳烃的污染特征

利用GC-MS对广州大学城珠江水域的地表水及表层沉积物中多环芳烃(PAHs)的含量进行了分析。结果表明,广州大学城珠江水域及表层沉积物中均可检出PAHs,水体优控PAHs总量在1061.7~6577.8ng/L之间,沉积物中优控PAHs总量分布在896.1~7248ng/g之间。广州大学城珠江水域的PAHs属混合来源,主要有石油类产品的输入(漏油泄油)和化石燃料的燃烧(大气沉降)。     

重点流域水系沉积物中多环芳烃标准样品制备

环境标准样品是监测过程中重要的质量控制手段,中国受天然基体标准样品制备技术的制约,尚未拥有自己的沉积物中多环芳烃标准样品。为制备符合中国重点流域沉积物类型及多环芳烃浓度水平的沉积物标准样品,对中国6个重点流域的沉积物进行了采样,获得了制备多环芳烃标准样品的原料。分析常温及冷冻2种干燥方式对多环芳烃的影响,为制备大批量多环芳烃标准样品提供数据支持。对11个点位样品采用气相色谱质谱法测定16种优控多环芳烃化合物浓度,结果表明,样品均匀性良好,样品中多环芳烃检出率在99%以上,江河沉积物样品中多环芳烃浓度区间为664~2.91×103μg/kg,湖泊样品最高值达到1.25×105μg/kg,其主要污染源是化学燃料的燃烧。为中国制备水系沉积物中多环芳烃标准样品积累了技术基础。     

气溶胶与降尘中多环芳烃的含量分布研究

通过广东省茂名市区四个不同功能点大气气溶胶和降尘中多环芳烃的含量分布研究发现 :1、气溶胶中优控多环芳烃大大高于降尘中的含量 ,为降尘的 5.97～ 1 9.3倍 ;以石化厂区为例 ,非优控多环芳烃在气溶胶中的相对含量更高 ,为降尘的 2 4 .7倍。2、气溶胶中优控多环芳烃和非优控多环芳烃的分布为随分子量增加而含量增高的趋势 ,但降尘中优控多环芳烃的高含量相对集中于萤蒽至苯并 (b)萤蒽之间。3、不同功能区由于排放源的差别所表现出的气溶胶和降尘中优控多环芳烃总量及总量比值、部分强致癌和致癌物含量及含量比值均存在差异。4、对气溶胶和降尘中多环芳烃研究可以对降尘中非优控多环芳烃降解和溶解量进行估算。以石化厂区为例 ,降尘中非优控多环芳烃比原始含量已减少76%。     

黄河兰州段水环境中多环芳烃污染初步研究

2004年11月对黄河兰州段11个采样点的水样、悬浮颗粒物和表层沉积物中的多环芳烃(PAHs)污染作了初步研究。调查结果显示,在此河段中,16种优先控制的PAHs均有检出,总PAHs浓度范围分别为水中,2920~6680ng/L;表层沉积物中,960~2940ng/g(干重);悬浮物中,4145~29090ng/g(干重);其中含量较高的是和芘,且分子量较小的PAHs所占的比例较大。来源分析结果显示,黄河兰州段水环境中PAHs的来源是燃烧源和石油源混合的结果,为混合输入型。用生物学阈值对表层沉积物质量进行评价,黄河兰州段表层沉积物的PAHs污染不算严重,偶尔会产生负面生态效应。     

山美水库流域表层沉积物中DDTs农药的残留特征及风险评估

利用GC-ECD检测了山美水库流域表层沉积物中DDTs农药含量,分析了其残留与组成特征及生态风险.结果表明,表层沉积物中DDTs平均含量为4.07 ng/g,其含量范围为0.96～8.20 ng/g;DDTs含量大小顺序为桃溪与湖洋溪汇流(8.20 ng/g)>湖洋溪(4.67 ng/g)>桃溪(4.59 ng/g)>山美水库(1.96 ng/g).表层沉积物中新的DDTs输入量比较少;沉积物中DDTs主要来自于早期残留或是施用农药长期风化后的土壤;大多数采样点DDTs发生好氧生物降解,降解产物以DDE为主.对照Ingersoll风险评估标准,表层沉积物中DDTs农药残留具有较高的生态风险.     

Polycyclic aromatic hydrocarbons in surface water and bed sediments of the Hungarian upper section of the Danube River

This study was performed to elucidate the distribution, concentration trend and possible source of polycyclic aromatic hydrocarbons (PAHs) in surface water and bed sediments of the Hungarian upper section of the Danube River and the Moson Danube branch. A total of 217 samples (water and sediments) were collected from four different sampling sites in the period of 2001–2010 and analysed for the 16 priority US Environmental Protection Agency PAHs. Concentrations of total 16 PAHs (∑PAHs) in water samples ranged from 25 to 1,208 ng/L, which were predominated by two- and three-ring PAHs. The ∑PAH concentrations in sediments ranged from 8.3 to 1,202.5 ng/g dry weight. Four-ring PAHs including fluoranthene and pyrene were the dominant species in sediment samples. A selected number of concentration ratios of specific PAH compounds were calculated to evaluate the possible sources of PAH contamination. The ratios reflected a pattern of pyrogenic input as a major source of PAHs. The levels of PAHs determined were compared with other sections of the Danube and other regions of the world.     

Distributions, sources and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in topsoil at Ji’nan city, China

Surface soil (0-5 cm) samples from 17 sampling sites including different functional areas at Ji'nan city in Shandong Province of China were collected and analyzed for 16 EPA priority polycyclic aromatic hydrocarbons (PAHs). The total PAH concentrations were in the range from 1.31 mg kg(-1) to 254.08 mg kg(-1) (dry weight), and the average level of total PAHs was 23.25 mg kg(-1). The highest total PAHs concentrations were found in steel and iron plant at industrial areas. The total PAHs concentrations in industrial areas were markedly higher than those in other different functional areas. According to comparing total PAHs concentration in Ji'nan city to that of other urban areas, it was found that total PAHs concentrations were 6 to 137 times higher than other areas because of some specific sampling sites such as steel and iron plant and one main roadside. The results showed that PAHs in topsoil of Ji'nan city were suffered from strong pyrogenic influence, especially in industrial areas. However about 52.9% soil samples were mainly originated from both pyrogenic and petrogenic mixed sources based on Flu/Pyr ratios and Phe/Ant ratios. Furthermore, It was found that all individual PAHs except Fle were significantly correlated (P < 0.01) with LMW, HMW, total PAHs and SOM, and individual PAHs except Fle in soils were significantly correlated (P < 0.01) with each other. The nemerow composite index to assess the environmental quality showed that the soil sample of steel and iron plant in industrial areas and one main roadside were heavy pollution of PAHs, and about 47% soil sampling sites were safety, about 53% soil sampling sites were got different grades of PAHs pollution.     

Polycyclic aromatic hydrocarbons and ecotoxicological characterization of sediments from the Huaihe River, China

The distribution, source, ecological risk and ecotoxicity of polycyclic aromatic hydrocarbons (PAHs) of sediments from 7 sampling sites, named as Xinyang (XY), Huainan (HN), Bengbu (BB), Xuyi (XuY), Fuyang (FY), Mengcheng (MC) and Zhengzhou (ZZ), in the Huaihe River basin, China, have been investigated. The total concentrations of 16 USEPA priority PAHs ranged from 62.9 to 2232.4 ng g?1 dry weight (d.w.) with a mean concentration of 1056.8 ng g?1 d.w. Through the assessment of ecological risk, we found that the levels of PAHs in the Huaihe River should not exert adverse biological effects. The total benzo[a]pyrene toxicity equivalent (TEQ) values calculated for samples varied from 0.01 to 194.1 ng g?1 d.w., with an average of 65.9 ng g?1. The toxicity data were accordant with the chemical analysis results in this study. HN, BB and ZZ showed the greatest pollution extent both in the chemical analysis and the study of ecotoxicological effects.     

淮南市大气PM_(10)中多环芳烃污染特征的研究

对2008年05至11月淮南市5个采样点大气可吸入颗粒物(PM10)样品进行分析,总结了研究区内PM10及其中16种PAHs的浓度特征、季节变化规律和来源解析。研究区内16种PAHs浓度总和的范围在15.20~111.58ng.m-3之间,平均值为40.40ng.m-3,中位数为33.34ng.m-3。PAHs总量的季节变化与采样时环境温度显示出较好的负相关性,即秋季>春季>夏季;运用多环芳烃比值综合判断,淮南市大气PM10中PAHs主要以燃煤和机动车尾气混合来源为主,石油源和木材燃烧来源的贡献较小。     

Concentration, distribution and source apportionment of atmospheric polycyclic aromatic hydrocarbons in the southeast suburb of Beijing, China

Total suspended particle samples and gas phase samples were collected at three representative sampling sites in the southeastern suburb of Beijing from March 2005 to January 2006. The samples were analyzed for 16 US EPA priority PAHs using GC/MS. Concentrations of Sigma PAHs in particle and gas phases were 0.21-1.18 x 10(3) ng m(-3) and 9.5 x 10(2) ng-1.03 x 10(5) ng m(-3), respectively. PAH concentrations displayed seasonal variation in the order of winter>spring>autumn>summer for particle phase, and winter>autumn>summer>spring for gas phase. Partial correlation analysis indicates that PAH concentrations in particle phase are negatively correlated with temperature and positively correlated with air pollution index of SO(2). No significant correlation is observed between gas phase PAHs and the auxiliary parameters. Sources of PAH are identified through principal component analysis, and source contributions are estimated through multiple linear regression. Major sources of atmospheric PAHs in the study area include coal combustion, coke industry, vehicular emission and natural gas combustion.     

Distribution and sources of polycyclic aromatic hydrocarbons in Wuhan section of the Yangtze River, China

Polycyclic aromatic hydrocarbons (PAHs) are important organic contaminants with great significance for China, where coal burning is the main source of energy. In this study, concentrations, distribution between different phases, possible sources and eco-toxicological effect of PAHs of the Yangtze River were assessed. PAHs in water, suspended particulate matters (SPM) and sediment samples at seven main river sites, 23 tributary and lake sites of the Yangtze River at the Wuhan section were analyzed. The total concentrations of PAHs in the studied area ranged from 0.242 to 6.235 μg/l in waters and from 31 to 4,812 μg/kg in sediment. The average concentration of PAHs in SPM was 4,677 μg/kg, higher than that in sediment. Benzo(a)pyrene was detected only at two stations, but the concentrations were above drinking water standard. The PAHs level of the Yangtze River was similar to that of some other rivers in China but higher than some rivers in foreign countries. There existed a positive relationship between PAHs concentrations and the TOC contents in sediment. The ratio of specific PAHs indicated that PAHs mainly came from combustion process, such as coal and wood burning. PAHs may cause potential toxic effect but will not cause acute biological effects in sedimentary environment of the Wuhan section of the Yangtze River.     

Spatial distribution and seasonal variation of polycyclic aromatic hydrocarbons (PAHs) contaminations in surface water from the Hun River, Northeast China

The objectives of this study were to investigate the levels, dispersion patterns, seasonal variation, and sources of 16 priority polycyclic aromatic hydrocarbons (16 EPA-PAHs) in the Hun River of Liaoning Province, China. Samples of surface water were collected from upstream to downstream locations, and also from the main tributaries of the Hun River in dry period, flood period, and level period, respectively. After appropriate preparation, all samples were analyzed for 16 EPA-PAHs. Total PAHs concentrations varied from 124.55 to 439.27 ng l^?1 in surface water in dry period, 1,615.75 to 5,270.04 ng l^?1 in flood period, and 2,247.42 to 7,767.9 ng l^?1 in level period. The 16 EPA-PAHs concentrations were significantly increased in the order of level period > flood period > dry period. The composition pattern of PAHs in surface water was dominated by low molecular weight PAHs, in particular two- to three-ring PAHs. In addition, two-ring PAH accounted for 39.33 to 88.27 % of the total PAHs in level period. Low molecular weight PAHs predomination together with higher levels of PAHs in flood and level period suggested a relatively recent local source of PAHs. Special PAHs ratios such as phenanthrene/anthracene and fluoranthene/pyrene indicated that under dry weather season conditions, the PAHs found in surface water were primarily from petrogenic source, while under wet weather season conditions they were from mixed source of both petrogenic inputs and combustion sources. The comparison of PAHs contamination among different types of areas in China suggested that atmospheric depositions might be the most important approaches of PAHs into water system. Although the Hun River exists low PAHs ecological risk now, potential toxic effects will be existed in the future especially in flood and level period.     

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.     

Distribution and risk assessment of polycyclic aromatic hydrocarbons (PAHs) from Liaohe estuarine wetland soils

Thirty-one surface soil samples were collected from Liaohe estuarine wetland in October 2008 and May and August 2009. The concentrations of 16 polycyclic aromatic hydrocarbons (PAHs), identified as priority pollutants by the US EPA, were measured by gas chromatography. PAHs were predominated by three- and four-ring compounds. The total PAH concentrations ranged from 704.7 to 1,804.5 μg/kg with a mean value of 1,001.9 μg/kg in October 2008, from 509.7 to 1,936.9 μg/kg with an average of 887.1 μg/kg in May 2009, and from 293.4 to 1,735.9 μg/kg with a mean value of 675.4 μg/kg in August 2009. The PAH concentration detected at most sites shared the same pattern, with maximum concentrations during the autumn (October) and minimum concentrations during the summer (August). The ecological risk assessment of PAHs showed that adverse effects would occasionally occur in the soils from Liaohe estuarine wetland based on the effects range low (ERL)/effects range median and the toxic equivalency factors. The results revealed that some of the individual PAHs were in excess of ERL which implied possible acute adverse biological effects. The BaP(eq) values in some sites surpassed the Dutch target value. Therewith, quite a part of soils in the wetland were subjected to potential ecological risks.