How should environmental exposure risk be assessed? A comparison of four methods for exposure assessment of air pollutions

Methods commonly used to assess the environmental exposure risk at a location (e.g., proximity models) are usually based on different assumptions, leading to conflicting results and recommendations in epidemiological studies. In this case study, a comparative evaluation of the accuracy levels associated with four commonly used exposure risk estimate models [i.e., traditional proximity model (TPM), emission weighted proximity model (EWPM), the American Meteorological Society/EPA regulatory model (AERMOD), and ordinary kriging interpolation (OKI)] were conducted. Results show that at the annual and the monthly scales, the normalized exposure risk values simulated by AERMOD and EWPM have higher accuracy levels than the simulations from the TPM and OKI methods. However, AERMOD has higher accuracy than that of the EWPM, and this was attributed to the differences of input data. EWPM provided the most accurate simulations when analysts have access to only point emission source data. The results also indicate that the accuracies of the exposure risks simulated by AERMOD and EWPM can be influenced by factors such as the modeling extent, the distance settings, and so forth.     

飞信通讯手段在突发环境污染事件处置时的应用

对现有移动通讯方式在突发环境污染事件中的应用进行了比较。通过实例,简述了飞信作为突发环境污染事件应急处置时通讯方式的应用。结果表明,飞信综合了一对一、多对多的语音和图文信息传输方式,在技术资料支持和监测结果通报方面具有明显的实用价值,配合防爆型对讲机,可以满足应对突发环境污染事件时对通讯的要求。     

“十一五”期间新疆大气降尘量时空分布特征及影响因素分析

通过对"十一五"期间新疆134个大气降尘监测点位数据进行统计分析发现,"十一五"期间,全疆年均降尘量维持在22.2~24.6 t/km2.月,变化幅度小于10%。一年内降尘主要集中在3~6月份,占全年降尘量的51%。在空间分布上,新疆年均降尘量呈现明显的南疆高于北疆的特征,南疆五地、州的总降尘量占全疆总降尘量的70.2%,为新疆降尘的主要集中区。特殊的气象、生态环境是决定新疆大气降尘时空分布特征的主要因素。     

Chemical compositions and sources of atmospheric PM10 in heating, non-heating and sand periods at a coal-based city in northeastern China

Mass concentrations and chemical components (18 elements, 9 ions, organic carbon [OC] and elemental carbon [EC]) in atmospheric PM(10) were measured at five sites in Fushun during heating, non-heating and sand periods in 2006-2007. PM(10) mass concentrations varied from 62.0 to 226.3 μg m(-3), with 21% of the total samples' mass concentrations exceeding the Chinese national secondary standard value of 150 μg m(-3), mainly concentrated in heating and sand periods. Crustal elements, trace elements, water-soluble ions, OC and EC represented 20-47%, 2-9%, 13-34%, 15-34% and 13-25% of the particulate matter mass concentrations, respectively. OC and crustal elements exhibited the highest mass percentages, at 27-34% and 30-47% during heating and sand period. Local agricultural residuals burning may contribute to EC and ion concentrations, as shown by ion temporal variation and OC and EC correlation analysis. Heavy metals (Cr, Ni, Zn, Cu and Mn) from coal combustion and industrial processes should be paid attention to in heating and sand periods. The anion/cation ratios exhibited their highest values for the background site with the influence of stationary sources on its upper wind direction during the sand period. Secondary organic carbon were 1.6-21.7, 1.5-23.0, 0.4-17.0, 0.2-33.0 and 0.2-21.1 μg m(-3), accounting for 20-77%, 44-88%, 4-77%, 8-69% and 4-73% of OC for the five sampling sites ZQ, DZ, XH, WH and SK, respectively. From the temporal and spatial variation analysis of major species, coal combustion, agricultural residual burning and industrial emission including dust re-suspended from raw material storage piles were important sources for atmospheric PM(10) in Fushun at heating, non-heating and sand periods, respectively. It was confirmed by principal component analysis that coal combustion, vehicle emission, industrial activities, soil dust, cement and construction dust and biomass burning were the main sources for PM(10) in this coal-based city.     

杭州城区春节PM2.5中水溶性离子在线观测

利用大气细颗粒物水溶性组分在线连续监测分析系统(AIM-URG9000D),考察了杭州城区春节期间PM2.5中无机水溶性离子的浓度变化范围,探讨了这些离子的日变化特征和影响因素,同时分析了集中燃放烟花爆竹对水溶性离子浓度的影响。结果表明,SO2-4、NO-3、NH+4是PM2.5中水溶性离子的主要成分,分别占全部水溶性组分的33.3%、28.4%、19.4%;强致癌物质NO-2浓度为2.07μg/m3,远大于膜采样结果;NO-3与SO2-4的质量比为0.85,表明机动车尾气排放导致的大气污染正逐步加重;各水溶性离子有着各自不同的日变化规律。相关性分析表明,NH+4与NO-3、SO2-4的相关系数分别为0.92、0.81;K+、Cl-、Mg2+3者之间的相关系数均在0.9以上。烟花爆竹燃放期间,PM2.5浓度急剧上升,Cl-、SO2-4、K+、Mg2+浓度分别达到燃放前的18、6、53、76倍。     

构建覆盖国家环境监测网的质量控制体系

"十二五"期间,中国将全面完成国家环境监测网的布局与建设,环境管理将开始由以环境污染控制为目标导向,向以环境质量改善为目标导向转变,以全面考核空气、水环境和土壤等环境质量的新环境管理时代即将来临。从现有环境监测质控体系所发挥的作用、存在的问题以及环境管理的需求出发,提出构建覆盖国家环境监测网的质量控制体系,论述各级环境监测站的质控职责,尤其是省级监测站作为地区质量控制中心,应该和国家站一起加大自身质控能力建设,为提高环境监测数据的可信度做好质控工作。     

“基于质谱技术的全组分痕量重金属分析仪器开发和应用示范”项目进展

介绍了国家重大科学仪器设备开发专项"基于质谱技术的全组分痕量重金属分析仪器开发和应用示范"项目在电感耦合等离子体质谱仪(ICP-MS)研发、低温等离子体样品引入ICP-MS联用系统、ICP-MS监测汞的采样与预处理等方面的研究进展,并对ICP-MS应用发展及产业化前景进行了展望。     

固相萃取-高效液相色谱法测定废水中的酚类化合物

建立了Supelclean ENVI-Chrom P柱固相萃取-高效液相色谱法测定废水中11种酚类化合物的分析方法,并对固相萃取条件和液相色谱条件进行了讨论。该方法分离效果良好,净化效果明显,方法检出限为2×10-3~2×10-2mg/L,平行分析(n=6)的RSD为2.7%~16.4%,废水加标回收率除2,4-二硝基酚偏低以外,其他化合物的回收率为61.4%~115.8%。     

气质联用法测固定污染源中三氟甲烷、四氟甲烷、六氟乙烷和六氟化硫

建立了固定污染源排气中三氟甲烷、四氟甲烷、六氟乙烷和六氟化硫的采样和气质联用分析方法,检出限分别为0.06、0.15、0.21、0.71 mg/m3,精密度在3.2%以下,相关系数大于0.999 6,并对浙江省内2家典型企业排放的温室气体进行了监测,实际样品监测结果表明,该方法能够满足废气中4种温室气体的监测要求。     

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.