山西省空气污染物PM_(2.5)时空分布特征研究

基于山西省11个地级市2015年7月至2016年5月的PM_(2.5)月均浓度数据,运用地理信息系统(GIS)和分级统计法分析了山西省PM_(2.5)的时空变化特征。结果表明:山西省PM_(2.5)月平均浓度变化具有季节性,2015年8—9月和2016年4—5月污染较轻,2015年12月至2016年1月污染较严重;晋南各城市污染均比较严重,而位于晋北的大同市和晋西的吕梁市PM_(2.5)月均浓度一直处于达标状态。主成分分析发现,除吕梁市外,其他地级市对山西省PM_(2.5)污染的贡献接近,表明不同地级市的PM_(2.5)月均浓度变化主要受大尺度的天气变化影响。研究结果有利于了解山西省PM_(2.5)污染的时空分布格局,进而有助于针对性地开展污染防控工作。     

冬季沈阳市典型源排放PM_(10)浓度分布模拟分析

选取沈阳市7个典型的大气污染源2006年12月~2007年2月的PM10排放浓度资料,利用CALPUFF对PM10浓度月平均分布做模拟分析。模拟结果分析表明:冬季月平均PM10浓度分布的范围与风场、地形有直接的关系。地势平坦、风速大时,污染物扩散范围大,污染物浓度小;地势不平、风速小时,污染物扩散范围小,污染物浓度大。1月份是沈阳市冬季月平均大气污染最严重的月份,污染物分布主要集中在市区的北部、东部和南部地区,东部地区大气污染最为严重。     

贵阳市白云区大气PM_(10)和PM_(2.5)污染特征

使用β射线法在线监测仪连续监测了贵阳市白云区PM_(10)和PM_(2.5)浓度,分析了2014年6月1日—12月31日7个月内PM_(10)、PM_(2.5)的浓度水平、时变规律和PM_(2.5)/PM_(10)的变化情况。结果表明,监测时段内PM_(10)和PM_(2.5)的日均浓度平均值分别为76.8μg/m~3和40.0μg/m~3,均达到国家二级标准;浓度超标的天数占总观测天数的5.1%和9.3%,属污染轻微的地区。PM_(2.5)/PM_(10)在25.3%~78.8%之间周期性波动,平均值为52.1%。PM_(10)和PM_(2.5)的浓度变化具有很好的正相关性(r=0.919 8,p0.000 1);日均值在7个月中呈现明显的周期性变化,各月相对稳定,12月的PM_(10)和PM_(2.5)浓度最高且变化最为剧烈,6月最为平缓。PM_(10)和PM_(2.5)浓度小时变化总体上呈双峰型分布,最高值出现在出现在09:00—10:00和19:00—21:00前后,最低值出现在14:00—17:00之间。     

区域大气环境中PM_(2.5)/PM_(10)空间分布研究

提出了一种利用移动监测技术研究区域大气环境中PM2.5/PM10空间分布的方法,并在2004年12月进行了宁波市全市域PM2.5/PM10空间分布的研究.数据显示:相同路径所代表的地区PM2.5和PM10具有很好的相关性,多数路径上PM2.5与PM10数据的相关系数平方在0.95以上,而不同路径上PM2.5与PM10的比值不同.文中给出了宁波市PM2.5/PM10污染的空间分布图,直观地显示出PM2.5/PM10污染的空间分布情况,突出了污染的重点点位和地区.     

北京地铁车厢内PM_(2.5)和PM_(10)污染特征研究

地铁是人们出行的重要交通方式,车厢内颗粒物污染可影响人体健康。2016年春、秋、冬季对北京地铁1号、2号、4号、10号线进行现场监测,探讨北京地铁车厢内颗粒物污染特征。研究结果表明,北京地铁车厢内PM_(2.5)平均浓度超标率为83.8%~98.7%,地铁1号线PM_(10)平均浓度超标率为59.6%。地铁车厢内PM_(2.5)和PM_(10)浓度存在工作日和周末组间显著性差异,表明客运量对车厢内颗粒物浓度有较大影响。地铁车厢内PM_(2.5)和PM_(10)浓度存在季节性差异,冬季车厢内颗粒物平均浓度最高。不同线路车厢内PM_(2.5)和PM_(10)浓度存在组间差异,地铁通风空调系统、门系统和客运量是造成其差异的主要原因。     

不对称街谷内PM_(2.5)浓度垂直分布特征及成因

当前细颗粒物PM2.5已成为城市环境的主要污染物,研究城市不对称街谷内PM2.5浓度的垂直分布特征,对居民日常生活与健康出行有现实意义。实验选取2013年3个不同阶段对高度在1~35 m范围的街谷进行PM2.5浓度监测,同时引用街谷内流场模型与浓度场模型,对PM2.5浓度垂直分布特征及成因进行探究。结果表明,不对称街谷受大气对流、风速、风向影响,街谷内细颗粒物存在不均匀分布特点,在较高侧随着壁面高度的增加PM2.5浓度大体呈S型曲线变化。同时在同一阶段监测的4天中街谷内PM2.5浓度分布特征大体一致,而阶段之间差异明显;街谷内PM2.5浓度垂直分布的最高浓度差出现在阶段1,高达75μg/m3,阶段2与阶段3浓度差相对减弱,仅在20~30μg/m3之间。通过阶段2与阶段3对比可知,北京冬季供暖燃煤对大气细颗粒物的贡献较大,导致颗粒物浓度偏高;而非采暖期气温回升,大气对流作用较强,有助于大气颗粒物扩散,因而街谷内PM2.5污染程度相对较低。     

空气中PM_(10)浓度的BP神经网络预报研究

建立了某市PM10浓度预报的分段BP神经网络模型,经验证,所建立的BP预报模型,预测精度比较高,PM10日平均浓度误差大多在-0．010～0．010mg／m^3范围内,相对误差在-20％～20％,表明BP神经网络对PM10的浓度预报是一种有效的工具。     

京津冀地区AOD和PM_(2.5)质量浓度的特征及相关性分析

为了探讨京津冀地区AOD和PM_(2.5)的变化特征及其相关性对NASA MODIS气溶胶光学厚度产品与京津冀地区PM_(2.5)质量浓度进行了比较分析。结果表明,AOD和PM_(2.5)均有明显的时间和空间分布特征且二者变化特征一致:张家口、承德、秦皇岛是观测期间2014年11月—2015年3月污染最轻的3个城市;京津冀南部AOD值和PM_(2.5)质量浓度明显高于北部。通过各市AOD和PM_(2.5)质量浓度的相关性分析,其最优模型均是非线性模型。根据各市最优模型得到的决定系数,邢台市、衡水市和石家庄市AOD和PM_(2.5)质量浓度具有比较好的相关性,北京市和天津市的相关性相对较差。     

大气PM_(2.5)遥感反演研究进展

PM_(2.5)是中国空气质量的重要评价指标,影响着环境和人体健康。近年来,遥感反演已逐渐成为监测PM_(2.5)的热点。介绍了大气PM_(2.5)反演常用的遥感数据优缺点及适用范围,对遥感反演方法进行归纳和总结,阐述构建PM_(2.5)与气溶胶光学厚度关系模型、消除气象因素和垂直分布等参数影响的方法,并展望PM_(2.5)遥感反演在高时空分辨率数据和模型耦合等方面的发展趋势。     

PM_(2.5)遥感反演技术研究进展

PM2.5是表征空气质量最为重要的指标之一。近年来随着卫星遥感技术的迅速发展,通过气溶胶光学厚度(AOD)间接反演PM2.5已成为监测PM2.5的重要技术手段。从遥感反演PM2.5基本原理、遥感数据源、PM2.5时空分布计算方法以及发展趋势4个方面对PM2.5遥感反演技术的研究进展进行了综述。     

Use of principal component analysis to profile temporal and spatial variations of chlorinated solvent concentration in groundwater

This work aims at evaluating spatial distribution patterns of concentration variations for chlorinated solvents in groundwater, based on principal component analysis and geographic information system (GIS) tools. The study investigates long-time series of chlorinated solvent concentrations in groundwater measured for 18 contaminated industrial sites. The characterization of contaminant plumes and delineation of pollutant sources are essential for choosing appropriate monitoring and remediation strategies, as contaminated groundwaters are characterized by complex patterns of spatial and temporal concentration variability, with wide unpredictable fluctuations over time. The present work describes the results of a new exploratory statistical method called the Variability Index Method (VIM) applied to environmental data to assess the performance of using concentration variations as molecular tracers to reveal aquifer dynamics, industrial impacts, and point sources for contamination plumes. The application of this method provides a useful assessment of controls over contaminant concentration variations as well as support for remediation techniques.     

Open burning and open detonation PM10 mass emission factor measurements with optical remote sensing

Emission factors (EFs) of particulate matter with aerodynamic diameter ≤10 µm (PM₁₀) from the open burning/open detonation (OB/OD) of energetic materials were measured using a hybrid-optical remote sensing (hybrid-ORS) method. This method is based on the measurement of range-resolved PM backscattering values with a micropulse light detection and ranging (LIDAR; MPL) device. Field measurements were completed during March 2010 at Tooele Army Depot, Utah, which is an arid continental site. PM₁₀ EFs were quantified for OB of M1 propellant and OD of 2,4,6-trinitrotoluene (TNT). EFs from this study are compared with previous OB/OD measurements reported in the literature that have been determined with point measurements either in enclosed or ambient environments, and with concurrent airborne point measurements. PM₁₀ mass EFs, determined with the hybrid-ORS method, were 7.8?×?10^?3 kg PM₁₀/kg M1 from OB of M1 propellant, and 0.20 kg PM₁₀/kg TNT from OD of TNT. Compared with previous results reported in the literature, the hybrid-ORS method EFs were 13% larger for OB and 174% larger for OD. Compared with the concurrent airborne measurements, EF values from the hybrid-ORS method were 37% larger for OB and 54% larger for OD. For TNT, no statistically significant differences were observed for the EFs measured during the detonation of 22.7 and 45.4 kg of TNT, supporting that the total amount of detonated mass in this mass range does not have an effect on the EFs for OD of TNT.

Implications: Particulate matter (PM) in the atmosphere affects the health of humans and ecosystems, visibility, and climate. Fugitive PM emissions are not well characterized because of spatial and temporal ubiquity and heterogeneity. The hybrid-ORS method is appropriate for quantifying fugitive PM emission factors (EFs) because it captures the spatial and temporal dispersion of ground level and elevated plumes in real time, without requiring numerous point measurement devices. The method can be applied to provide an opportunity to reduce the uncertainty of fugitive PM EFs and readily update PM emissions in National Emission Inventories for a range of fugitive PM sources.     

Spatial and temporal variations in PM10 and PM2.5 source contributions and comparison to emissions during the 1995 integrated monitoring study

The ambient PM₁₀ and PM_2.5 data collected during the fall and winter portions of the 1995 Integrated Monitoring Study (IMS95) were used to conduct Chemical Mass Balance (CMB) Modeling to determine source contribution estimates. Data from the core and saturation monitoring sites provided an extensive database for evaluating the spatial and temporal variations of contributing sources. Geological sources dominated fall samples, while secondary ammonium nitrate and carbonaceous sources were the largest contributors for winter samples. Secondary ammonium nitrate concentrations were uniform across all sites during both the fall and winter. Site-to-site variability was primarily due to differences in geological contributions in the fall, and carbonaceous source contributions in the winter. During the winter, diurnal profiles of particulate matter (PM) were driven by variations in carbonaceous sources at urban sites, and by variations in secondary ammonium nitrate at rural sites. Although records of day-specific PM activities were recorded during the study, no correlation was observed between 24-h CMB results and specific activities. The ambient data collected during IMS95 was also used to evaluate the adequacy of the emissions inventory. Comparison of ambient and emissions based ratios of NMHC/NO_x, PM/NO_x, CO/NO_x, and SO_x/NO_x suggested that emissions of NMHC and CO in some locations may be underestimated, while emissions for PM and SO_x may be overestimated. Comparison of fractional primary CMB source contribution estimates to corresponding fractional emissions estimates indicated that geological sources were overemphasized in the inventory, while carbonaceous sources were underrepresented.     

基于BP人工神经网络的城市PM2.5浓度空间预测

针对PM2.5日均质量浓度,采用BP人工神经网络模型,预测研究区空气中PM2.5浓度的空间变异,通过与普通克里格(Ordinary Kriging)插值方法对比验证BP人工神经网络预测模型的精度.结果表明:BP人工神经网络预测模型下研究区检验样本点位置的PM2.5仿真浓度与观测浓度之间的均方差、平均绝对误差、平均相对偏差和相关系数分别为0.296 μg2/m6、0.412 μg/m3、1.650％和0.851;而与此同时,普通克里格插值方法下的对应结果分别为1.041 μg2/m6、0.689 μg/m3、11.910％、0.638.研究成果在肯定BP人工神经网络预测模型可用于揭示PM2.5浓度空间变异特征的同时,也证实了其相对于普通克里格插值方法在固定空间点位准确预测PM2.5浓度方面的优势.     

Source apportionment of PM10 and PM2.5 in five Chilean cities using factor analysis

Chile is a fast-growing country with important industrial activities near urban areas. In this study, the mass and elemental concentrations of PM10 and PM2.5 were measured in five major Chilean urban areas. Samples of particles with diameter less than 10 microm (PM10) and 2.5 microm (PM2.5) were collected in 1998 in Iquique (northern Chile), Valparaiso, Vi?a del Mar, Rancagua (central Chile), and Temuco (southern Chile). Both PM10 and PM2.5 annual mean concentrations (PM10: 56.9-77.6 microg/m3; PM2.5: 22.4-42.6 microg/m3) were significantly higher than the corresponding European Union (EU) and U.S. Environmental Protection Agency (EPA) air quality standards. Moreover, the 24-hr PM10 and PM2.5 U.S. standards were exceeded infrequently for some of the cities (Rancagua and Valparaiso). Elements ranging from Mg to Pb were detected in the aerosol samples using X-ray fluorescence (XRF). For each of the five cities, factor analysis (FA) was applied to identify and quantify the sources of PM10 and PM2.5. The agreement between calculated and measured mass and elemental concentrations was excellent in most of the cities. Both natural and anthropogenic sources were resolved for all five cities. Soil and sea were the most important contributors to coarse particles (PM10-PM2.5), whereas their contributions to PM2.5 were negligible. Emissions from Cu smelters and oil refineries (and/or diesel combustion) were identified as important sources of PM2.5, particularly in the industrial cities of Rancagua, Valparaiso, and Vi?a del Mar. Finally, motor vehicles and wood burning were significant sources of both PM2.5 and PM10 in most of the cities (wood burning was not identified in Iquique).     

Particulate matter in California: part 2--Spatial, temporal, and compositional patterns of PM2.5, PM10-2.5, and PM10

Geographic and temporal variations in the concentration and composition of particulate matter (PM) provide important insights into particle sources, atmospheric processes that influence particle formation, and PM management strategies. In the nonurban areas of California, annual-average PM2.5 and PM10 concentrations range from 3 to 10 microg/m3 and from 5 to 18 microg/m3, respectively. In the urban areas of California, annual-averages for PM2.5 range from 7 to 30 microg/m3, with observed 24-hr peaks reaching levels as high as 160 microg/m3. Within each air basin, exceedances are a mixture of isolated events as well as periods of elevated PM2.5 concentrations that are more prolonged and regional in nature. PM2.5 concentrations are generally highest during the winter months. The exception is the South Coast Air Basin, where fairly high values occur throughout the year. Annual-average PM2.5 mass, as well as the concentrations of major components, declined from 1988 to 2000. The declines are especially pronounced for the sulfate (SO4(2-)) and nitrate (NO3-) components of PM2.5 and PM10) and correlate with reductions in ambient levels of oxides of sulfur (SOx) and oxides of nitrogen (NOx). Annual averages for PM10-2.5 and PM10 exhibited similar downwind trends from 1994 to 1999, with a slightly less pronounced decrease in the coarse fraction.     

Impact assessment of meteorological and environmental parameters on PM2.5 concentrations using remote sensing data and GWR analysis (case study of Tehran)

Environmental Science and Pollution Research - The PM2.5 as one of the main pollutants in Tehran city has a devastating effect on human health. Knowing the key parameters associated with PM2.5...     

冬季沈阳市典型源排放PM10浓度分布模拟分析

选取沈阳市7个典型的大气污染源2006年12月～2007年2月的PM10排放浓度资料,利用CALPUFF对PM10浓度月平均分布做模拟分析。模拟结果分析表明：冬季月平均PM10浓度分布的范围与风场、地形有直接的关系。地势平坦、风速大时,污染物扩散范围大,污染物浓度小;地势不平、风速小时,污染物扩散范围小,污染物浓度大。1月份是沈阳市冬季月平均大气污染最严重的月份,污染物分布主要集中在市区的北部、东部和南部地区,东部地区大气污染最为严重。     

Characterization of PM2.5 and PM10 in the South Coast Air Basin of southern California: Part 1--Spatial variations

In December 1994, the South Coast Air Quality Management District (SCAQMD) initiated a comprehensive program, the PM10 Technical Enhancement Program (PTEP), to characterize fine PM in the South Coast Air Basin (SCAB). A 1-year special particulate monitoring project was conducted from January 1995 to February 1996 as part of the PTEP. Under this enhanced monitoring, HNO3, NH3, and speciated PM10 and PM2.5 concentrations were measured at five stations (Anaheim, downtown Los Angeles, Diamond Bar, Fontana, and Rubidoux) in the SCAB and at one background station at San Nicolas Island. PM2.5 and PM10 mass and 43 individual species were analyzed for a full chemical speciation of the particle data. The PTEP data indicate that the most abundant chemical components of PM10 and PM2.5 in the SCAB are NH4+ (8-9% of PM10 and 14-17% of PM2.5), NO3- (23-26% of PM10 and 28-41% of PM2.5), SO4- (6-11% of PM10 and 9-18% of PM2.5), organic carbon (OC) (15-19% of PM10 and 18-26% of PM2.5), and elemental carbon (EC) (5-8% of PM10 and 8-13% of PM2.5). On an annual average basis, PM2.5 comprises 52-59% of the SCAB PM10. Annual average PM10 and PM2.5 concentrations showed strong spatial variations, low at coastal sites and high at inland sites. Annual average PM10 concentrations varied from 40.8 micrograms/m3 at Anaheim to 76.8 micrograms/m3 at Rubidoux, while annual average PM2.5 concentrations varied from 21.7 micrograms/m3 at Anaheim to 39.8 micrograms/m3 at Rubidoux. The chemical characterizations of the PM2.5 and PM10 concentrations, as well as their spatial variations, were examined; the important findings are summarized in this paper, and the temporal variations are discussed in the companion paper.