多环芳烃在水稻籽粒中的分布及其与环境介质含量的关系

介绍了江西南昌某郊区采集的成熟期(2008年9月)和收割期(2008年10月)的水稻籽粒中多环芳烃(PAHs)的富集情况,并与同时期的环境介质(土壤、空气气相以及颗粒物)中多环芳烃的含量及分布情况作了相关性分析。结果表明,研究区水稻籽粒中16种多环芳烃(∑PAHs)总量平均为(74.8±13.6)ng/g,水稻土壤中∑PAHs含量平均为(203.7±14.3)ng/g,空气气相样品中∑PAHs含量平均为68.25 ng/m3,以3环和4环多环芳烃为优势化合物;颗粒物样品中∑PAHs含量平均为42.28 ng/m3,以4环、5环和6环多环芳烃为优势化合物。各介质多环芳烃含量在国内同类地区中均位于中等偏下水平。将多环芳烃在水稻籽粒和各个介质之间的生物富集系数与化合物的辛醇分配系数KOC、KOA作对数变换后比较,发现水稻籽粒中多环芳烃的分布与水稻土和空气颗粒物中的多环芳烃没有太大关系;而与空气气相中的多环芳烃关系较明显,证实了前人得到的气相化合物对植物体内化合物的分配起着主要贡献的研究结论。     

黄河兰州段水环境中多环芳烃来源解析

根据黄河兰州段水环境中多环芳烃的监测数据,对研究河段污染源排放特点进行了分析,采用比值法和轮廓图法对水环境中各介质(水体、悬浮颗粒物及底泥)中的多环芳烃进行了源解析,得出污染源主要来自石油及其炼制产品燃烧,有个别采样断面是石油及其炼制产品、煤、木碳燃烧等混和源所致.综合考虑源解析结果以及黄河兰州段工矿企业特点,提出了相应的多环芳烃治理措施,以期为研究河段水环境治理提供参考方法.     

原煤尾气和煤渣中多环芳烃相关性测定

对原煤、尾气和煤渣中多环芳烃进行了相关性测试。在模拟工业锅炉代表性燃烧条件下将烟煤和无烟煤样品在管式炉中燃烧，分别采用ＧＣＭＳ和ＨＰＬＣ法对原煤、尾气和煤渣中的多环芳烃种类和含量进行了定性和定量测定。通过在特定条件下某一煤种中多环芳烃种类、含量在燃前、燃后变化的相关性，探索煤中多环芳烃在燃烧过程中的衍变规律     

不同方法对提取原煤中PAHs分布的影响

选取超声提取法和索氏提取法,对淮北煤田主采煤层新鲜煤样中多环芳烃进行提取,并利用气相色谱-质谱联用仪对提取液中的多环芳烃进行定量分析,研究了不同方法对提取原煤中(US-EPA)优先控制的多环芳烃种类、质量分数和分布的影响。结果表明,在本实验条件下索氏提取法在提取原煤中多环芳烃能力上优于超声提取法。      

二叠纪—三叠纪界线大火燃烧的地层记录:研究进展回顾与评述

黑碳和燃烧源多环芳烃作为大火燃烧的产物有很强的化学惰性及生物惰性,能够在地层中长期稳定地保存,所以成为恢复古代大火历史的最常用指标。近年来世界各地二叠系—三叠系(P-Tr)界线地层中相继发现了黑碳(木炭等)和燃烧源多环芳烃等记录,特别是在煤山P-Tr界线地层,黑碳和燃烧源多环芳烃含量在生物灭绝线附近(25～26层)出现极高的峰值,据此首次明确地提出了P-Tr界线大火事件。P-Tr界线大火的规模、性质如何,与P-Tr界线生物灭绝有什么关系等,值得深入讨论和研究。大火事件发生在陆地上,通过其燃烧及排放的烟尘等,把陆地、大气和海洋密切联系起来,有利于通过系统的整体观来研究当时的气候环境变迁。因此,在回顾和总结P-Tr界线地层中的大火燃烧记录基础上,评述了大火事件与生物灭绝及相关地质事件和环境变化之间的联系,以期引起国内外专家学者的关注,为P-Tr界线生物灭绝及相关研究提供新的思路。     

第二松花江中下游河段底泥中多环芳烃的初步研究

第二松花江中下游河段8个底泥中多环芳烃（PAHs）分析表明，5种多环芳烃含量和多环芳烃总量随取样点位置发生明显的变化，城区河段底泥中各种PAHs含量和PAHs总量均高于非城区河段。2环加3环与5环PAHs化合物分布特点表明第二松花江中下游非城区河段底泥中PAHs的来源以石油类污染为主，而城区河段PAHs的来源则主要是化石燃料高温燃烧。第二松花江中下游河段（尤其是城区河段）底泥中PAHs具有较高生态风险，可能会对生物产生一定的负面影响。     

污染土壤中多环芳烃的微生物降解及其机理研究进展

多环芳烃(PAHs)是一类普遍存在于环境中的难降解危险性“三致”有机污染物。微生物对多环芳烃的降解是去除土壤中多环芳烃的主要途径。研究表明，对于土壤中低分子量多环芳烃类化合物，微生物一般以唯一碳源方式代谢；而大多数细菌和真菌对四环或四环以上的多环芳烃的降解作用一般以共代谢方式开始。本文重点论述了高分子量多环芳烃：芘和苯并(a)芘的微生物降解及其机理。并介绍了多环芳烃污染的微生物—植物联合修复机制，最后展望了污染土壤中多环芳烃的研究趋势。     

伊通地堑下第三系原油和生油岩中芳构化五环三萜及其地球化学意义

详细研究了吉林伊通地堑下第三系生油岩和原油中的芳烃生物标志物，包括常规的多环芳烃，以及丰富的来源于高等植物的芳香二萜和芳构化的五环三萜。目前，原油中芳构化五环三萜类生物类生物标志物国内外均尚报道极少。还详细讨论了利用原油中最新发现的芳构化五环三萜在解决本区生物输入，油源对比以及石油成因等方面的重要意义。     

北京密云房山地区土壤中多环芳烃的组成与分布特征

选择北京城近郊房山与密云地区的土壤进行了多环芳烃的定量分析，同时探讨了多环芳烃在土壤中的分布特征与来源。研究结果显示：密云、房山两地土壤中多环芳烃的含量值具有明显差异，提示了两地工业活动影响强度的不同；各采样区土壤中多环芳烃总量的平均值在45．98～388．23ng／g变化，根据多环芳烃的特征参数可以推测研究区土壤中的多环芳烃主要来自于化石燃料的不完全燃烧。     

贵阳市大气环境中颗粒态多环芳烃特征

多环芳烃(PAHs)类物质具有致癌性、致畸性、致突变性和生物累积性,能长期留存在环境中[1].燃煤是多环芳烃的主要来源,贵阳市特殊的能源结构、地形和气候条件,造成了典型的煤烟型大气污染,我们首次研究了贵阳市大气颗粒物中颗粒态PAHs的特征.     

Organic pollutants associated with macromolecular soil organic matter: Mode of binding

A study of ether-linked moieties in macromolecular bound residues of polycyclic aromatic hydrocarbons (PAH) generated in bioremediation experiments was performed using high temperature hydrolysis degradation with subsequent analysis of the products by GC-MS. This hydrolysis reaction was specifically designed to cleave ether bonds including relatively stable diarylether structures. Among the reaction products, aromatic alcohols representing typical microbiologically derived metabolites of PAH were found in addition to natural compounds. Thus, parts of the bound residues appeared to be linked within the macromolecular material by ether bonds. Model experiments with an oxidoreductase enzyme and aromatic alcohols indicate the formation of these ether bonds to be an enzyme-catalysed process.     

环境中的多环芳烃及其生物恢复技术

多环芳烃是一大类广泛存在于环境中的有机污染物。天然燃烧、火山爆发、矿物资料及其它有机物的不完全燃料和热解产生的PAH进入大气中，气态沉降、城市地表径流、城市污水、废水及油的溢涵和渗漏等是PAH进行地表水的主要途径，大气中PAH的干、湿沉降，污水灌溉，地面及地下储油装置的渗漏，地面固体废物堆的淋滤等是土壤中PAH的主要来源，沉积物和土壤是PAH的主要环境归宿。生物恢复是一种处理有机污染的新方法。     

The role of zooplankton fecal pellets in the sedimentation of polycyclic aromatic hydrocarbons in Dabob Bay,Washington

Polycyclic aromatic hydrocarbon (PAH) compositions were determined in plankton, sediment-trap-collected particulate material and sediment cores from Dabob Bay using a high performance liquid Chromatographie (HPLC)/fluorescence technique. The annual flux of individual PAH measured in a series of sediment traps was compared with the flux of corresponding compounds determined from ²¹⁰Pb dated bottom sediments. Systematic seasonal variations in the fluxes and concentrations of PAH, Al and organic carbon in the trap-collected particulates and seasonally collected plankton were also investigated to determine whether or not PAH are associated with either terrestrial or marine-derived materials.Concentrations of all PAH studied increased tenfold within the last 80–100 yr of sediment deposition, except for perylene which displayed a reasonably constant concentration profile. This suggests at least two sources contribute to the observed sedimentary PAH compositions in Dabob Bay, i.e., anthropogenic combustion and a natural source. Plankton and sediment trap-collected particulates contained PAH mixtures qualitatively similar to underlying surface sediments. Microscopic examination indicated fecal pellets were the major form of particulate material in the sediment traps. The fecal pellets collected in the sediment trap time series quantitatively account for essentially 100% of the PAH fluxes measured in the ²¹⁰Pb dated sediments, implying Zooplankton fecal pellets control the removal of PAH to Dabob Bay sediments. These measurements provide clear evidence that the PAH studied are not produced after sediment deposition. The observed seasonal covariations of PAH and Al in both sediment trap and plankton samples further indicate that PAH originate from terrestrially-based sources, are introduced into the marine environment by runoff and erosion or atmospheric deposition and are not produced by marine plankton.     

Polycyclic aromatic hydrocarbons in Recent lake sediments—I. Compounds having anthropogenic origins

Polycyclic aromatic hydrocarbons (PAH) in sediment cores from Lake Lucerne, Lake Zürich, and Greifensee, Switzerland, and Lake Washington, northwest U.S.A., have been isolated, identified and quantified by glass capillary gas chromatography and gas chromatography/mass spectrometry. Surface sediment layers are greatly enriched in PAH—up to 40 times—compared to deeper layers. In addition, concentration increases in upper sediments generally correspond to increasing industrialization and urbanization in the catchment basins of the lakes. Few PAH could be detected in pre-industrial revolution sediments, indicating that background levels for most PAH in aquatic sediments are extremely low.These results are consistent with an anthropogenic source for most of the aromatic hydrocarbons present in the modern sediments. A comparison of PAH distributions in the sediments and in possible source materials shows that urban runoff of street dust may be the most important PAH input to these lacustrine sediments. There is evidence that a significant contribution to the PAH content of street dust comes from material associated with asphalt.     

Enhanced biodegradation of polycyclic aromatic hydrocarbons using nonionic surfactants in soil slurry

The effect of nonionic surfactants on the solubility and biodegradation of polycyclic aromatic hydrocarbons (PAHs) in the aqueous phase and in the soil slurry phase, as well as the fate of these surfactants, were investigated. The PAH solubility was linearly proportional to the surfactant concentration when above the critical micelle concentration (CMC), and increased as the hydrophile–lipophile balance (HLB) value decreased. Substantial amounts of the sorbed phenanthrene in the soil particles were desorbed by non-ionic surfactants into the liquid phase when the ratio of soil to water was 1:10 (g/ml). Brij 30 was the most biodegradable surfactant tested, showed no substrate inhibition up to a concentration of 1.5 g/l, and was definitely used as a C source by the bacteria. Naphthalene and phenanthrene were completely degraded by phenanthrene-acclimatised cultures within 60 h, but a substantial amount of naphthalene was lost due to volatilization. The limiting step in the soil slurry bioremediation was bioavailability by the micro-organisms for the sand slurry and mass transfer from a solid to aqueous phase in the clay slurry.     

The global distribution of polycyclic aromatic hydrocarbons in recent sediments

Polycyclic aromatic hydrocarbons (PAH) and their alkyl homologs are distributed in sediments throughout the world. The qualitative PAH pattern is remarkably constant for most of the locations studied, and the quantitative PAH abundance increases with proximity to urban centers. These findings are consistent with anthropogenic combustion's being the major source of these compounds. Two non-combustion sources of PAH have also been noted: retene coming from abietic acid and perylene probably coming from various extended quinone pigments.     

对重金属和辐射污染的土壤和地下水的微生物修复

由重金属和辐射产生的环境污染在世界范围内产生了一系列问题.利用特殊的微生物如金属还原和耐金属细菌对环境中的金属和辐射污染进行处理具有非常好的前景.现场的生物修复的成功应用将对清除污染环境中的重金属和辐射提供潜在方法.最近的研究还关注于了解在微生物群体内重金属和辐射对微生物的作用.生物毯和生物膜是在生物修复中具有代表性的两种微生物群落的机能.金属的种类和价态变化、转移过程以及微生物代谢作用是对金属和辐射生物修复的三种重要的组成部分.结合以上三方面,可以更好的了解自然中的微生物和生物修复过程之间的关系.     

The polycyclic aromatic hydrocarbon concentrations in soils in the Region of Valasske Mezirici, the Czech Republic

The polycyclic aromatic hydrocarbon (PAH) contamination of urban, agricultural and forest soil samples was investigated from samples obtained in the surroundings of Valasske Mezirici. Valasske Mezirici is a town located in the north-east mountainous part of the Czech Republic, where a coal tar refinery is situated. 16 PAHs listed in the US EPA were investigated. Organic oxidizable carbon was also observed in the forest soils. The PAH concentrations ranged from 0.86-10.84 (with one anomalous value of 35.14) and 7.66-79.39 mg/kg dm in the urban/agricultural and forest soils, respectively. While the PAH levels in the urban/agricultural soils are within the range typically found in industrialized areas, the forest soils showed elevated PAH concentrations compared to other forest soils in Western and Northern Europe. The PAH concentrations and their molecular distribution ratios were studied as functions of the sample location and the meteorological history. The soils from localities at higher altitudes above sea level have the highest PAH concentrations, and the PAH concentrations decrease with increasing distance from the town.     

地下水有机污染治理技术现状及发展前景

概述了现有的几种地下水有机污染治理方法：抽出处理、注气－抽取土壤气、内在生物净化、流线控制、多技术结合法、生物治理、吸附、原位反应墙等工作原理和治理效果;简要分析了地下水有机污染治理技术存在的问题和发展前景。     

Effects of physical mixing on the attenuation of polycyclic aromatic hydrocarbons in estuarine sediments

To examine the role of physical disturbance on the long-term preservation of polycyclic aromatic hydrocarbons (PAHs) in sediments, cores were collected from two sites removed from point sources of PAHs and representing contrasting seabed mixing regimes. Although ΣPAH concentrations in sediments over the past 50 years were not significantly different between the two sites, several PAH isomer ratios were significantly different (P<0.05) between the two sites. Downcore changes in PAH isomer ratios resulted from preferential losses of the more linear PAH isomers. Thus, episodic, intense seabed mixing contributes to more efficient removal of selected PAHs. However, PAHs are still sufficiently stable relative to mixing events that historical PAH profiles can be used to reconstruct major resuspension events.