海口市PM_(10)、PM_(2.5)和PM_1质量浓度的变化特征分析

利用2013年在海口市气象局地面气象观测站采集的PM10、PM2.5和PM1质量浓度数据,分析了2013年可吸入颗粒物质量浓度的变化特征,并对其成因进行了初步分析。结果表明:2013年海口市PM10、PM2.5和PM1质量浓度的变化趋势基本相同,PM10、PM2.5质量浓度的超标率低,达到一级标准的概率分别为74.0%和68.8%,超过2级标准的天数分别为1和9 d,ρ(PM2.5)/ρ(PM10)与ρ(PM1)/ρ(PM2.5)的比例平均分别为78.1%和85.1%;海口PM10、PM2.5和PM1质量浓度冬季最高,夏季最低,春、秋两季处于冬夏之间;PM10、PM2.5和PM1质量浓度的日变化呈双峰现象,一个峰出现在上午,一个峰出现在夜间;颗粒物质量浓度的变化主要受到气象条件和污染物排放的影响。     

Ground-Based In Situ Measurements of Near-Surface Aerosol Mass Concentration over Anantapur: Heterogeneity in Source Impacts

Surface measurements of aerosol physical properties were made at Anantapur(14.62°N,77.65 °E,331 m a.s.l),a semiarid rural site in India,during August 2008-July 2009.Measurements included the segregated sizes of aerosolsas as well as total mass concentration and size distributions of aerosols measured at low relative humidity(RH<75%) using a Quartz Crystal Microbalance(QCM) in the 25-0.05 μm aerodynamic diameter range.The hourly average total surface aerosol mass concentration in a day varied from 15 to 70 μg m-3,with a mean value of 34.02±9.05μgm-3 for the entire study period.A clear diurnal pattern appeared in coarse,accumulation and nucleation-mode particle concentrations,with two local maxima occurring in early morning and late evening hours.The concentration of coarse-mode particles was high during the summer season,with a maximum concentration of 11.81±0.98μgm-3 in the month of April,whereas accumulationmode concentration was observed to be high in the winter period contributed >68% to the total aerosol mass concentration.Accumulation aerosol mass fraction,A f(=Ma/Mt) was highest during winter(mean value of Af～0.80) and lowest(Af～0.64) during the monsoon season.The regression analysis shows that both R eff and R m are dependent on coarse-mode aerosols.The relationship between the simultaneous measurements of daily mean aerosol optical depth at 500 nm(AOD500) and PM 2.5 mass concentration([PM2.5]) shows that surface-level aerosol mass concentration increases with the increase in columnar aerosol optical depth over the observation period.     

辽宁中部城市群可吸入颗粒物PM10和PM2.5的污染特征研究

利用2006年8月-2007年10月辽宁中部沈阳、鞍山、抚顺和本溪4城市可吸入颗粒物PM10、PM2.5、PM1及同步气象因子的监测资料,分析了可吸入颗粒物分布特征、污染水平及其与气象因子的关系。结果表明：受区域天气系统的影响,4城市PM10和PM2.5的日平均浓度变化趋势基本一致,具有区域分布特征;PM10超标率冬季为最高;PM2.5日平均浓度占PM10比例夏季和冬季最大;PM10、PM2.5和PM1之间有很好的相关性;PM10与风速、温度呈负相关,PM2.5和PM1与能见度、风速、温度呈负相关,与相对湿度成正相关。     

Using Föhn conditions to characterize urban and regional sources of particles

Characterizations of urban and regional sources of particulate matter (PM) were performed in the Milan area (North of Italy) during Föhn and stagnant (non-Föhn) conditions. The measurements were performed at two different places: in an urban area North of Milan (Bresso) and in a regional area at the EMEP-GAW station in Ispra (about 65 km NW from Milan) during the winter periods of the years 2002–2007. Particle size distributions and chemical bulk analysis of aerosols are combined with single particle mass spectrometry to obtain information about the chemical content of the particles and their mixing state. Föhn conditions are characterized by extremely clean background air from which background aerosol is scavenged, and consequently local sources (here defined as sources between the sampling sites and the mountain range top about 100–150 km away depending on the wind direction) determine the aerosol properties.It was observed that during Föhn events the accumulation mode in the size range 50 nm < d < 300 nm practically disappears and that the size fraction below 50 nm dominates the total number distribution. The significant change in the number size distribution and the large decrease in PM10 mass during Föhn events are accompanied by a significant change in the chemical composition of the particles. Results from bulk chemical analysis showed high amounts of carbonaceous compounds and very low concentrations of ammonium nitrate (as indicator for secondary chemistry) during Föhn episodes, in contrast to stagnant conditions, when secondary components are dominating the aerosol composition. Single particle measurements confirm the high contribution of carbonaceous compounds in locally emitted particles.It was concluded that particles that originated in the urban area come mainly from combustion processes, especially direct traffic emissions, domestic heating and industrial activities, whereas the regionally emitted particles are different with much less traffic contribution.We estimate that under prevailing (non-Föhn) winter conditions, about 50–65% of the aerosol mass load in the city of Milan are caused by local emissions, and about 35–50% come from regional background. This finding suggests that in order to improve air quality in a big city like Milan, it is important to combine local traffic restriction interventions with other long-term regional scale air-quality-measures.     

2007和2008年夏季北京奥运馆大气PM10与PM2.5质量浓度变化特征

为了监测北京奥运主场馆附近大气颗粒物的污染状况以及评估奥运污染源减排措施对北京大气颗粒物质量浓度变化的影响,利用颗粒物在线监测仪器TEOM于2007年和2008年夏季,在奥运主场馆附近的中国科学院遥感应用研究所办公楼楼顶对大气颗粒物PM10和PM2.5进行了连续同步观测。结果表明,2007年夏季监测点附近大气PM10与PM2.5质量浓度的平均值分别为153.9和71.2μg.m-3,而2008年夏季PM10与PM2.5质量浓度的平均值分别为85.2和52.8μg.m-3。与奥运前一年同时段相比,奥运时段大气PM10和PM2.5的质量浓度分别下降44.5%和25.1%。对比分析奥运前后的2次典型污染过程发现,空气相对湿度的增加和偏南气流输送的共同影响易造成大气颗粒物的累积增长,而降雨的湿清除作用和偏北气流则会使大气颗粒物浓度迅速降低。在相近的气象条件下,奥运前后的污染过程中,大气细粒子的日均增长速率分别为25.1和13.9μg.m-3.d-1,而大气粗粒子的日均增长速率分别为20.8和2.2μg.m-3.d-1,奥运时段污染累积过程中大气粗、细粒子的增长速率分别显著低于和略低于奥运前同时段污染过程中颗粒物的增长速率。污染源减排措施的实施是奥运期间大气颗粒物质量浓度降低的主要原因,从控制效果来看,奥运期间实施的污染源减排措施对大气粗粒子的控制效果明显好于大气细粒子。     

通辽市可吸入颗粒物质量浓度变化监测分析

文章基于通辽市2011年6月至2013年5月可吸入颗粒物质量浓度(PM10)资料数据,统计结果表明:(1)PM10年均质量浓度为85.92μg·m-3,未达到国家环境空气质量二级标准;(2)PM10季均质量浓度特征是春季冬季秋季夏季,PM10月平均质量浓度与季节分布基本一致;(3)PM10质量浓度在一周中呈现出单峰变化的特点,不同季节PM10质量浓度周变化不同;(4)PM10质量浓度日变化呈现双峰型分布。PM10浓度峰值从夏季到冬季逐渐推迟,这主要与日出日落时间和其他气象条件,以及上下班交通高峰相关;春季峰值还与沙尘天气发生时间有关。     

南京北郊冬季大气气溶胶及其湿清除特征研究

利用WPS(宽范围颗粒粒径谱仪)、雨滴潜仪和雾滴谱仪测量了2007～2008年冬季南京北郊大气气溶胶数浓度谱分布和降水强度,分析了气溶胶粒子的分布特征以及气溶胶粒径与湿清除系数的关系.结果表明:气溶胶粒子具有明显的双峰型R变化特征,数浓度主要集中在0.02～O.2μm粒径范围内,受汽车尾气排放、混合层高度变化以及颗粒物水平输送的影响较大.降雨、降雪和雾过程都对气溶胶粒子有不同程度的清除,降雨和浓雾对核模态和粗模态的气溶胶粒子的清除能力显著,降雪对粒径小于0.03μm的气溶胶粒子的清除能力较强.     

Aerosol spectra and new particle formation observed in various seasons in Nanjing

The aerosol number spectrum and gas pollutants were measured and the new particle formation （NPF） events were discussed in Nanjing. The results showed that the size distributions of aerosol number concen- trations exhibited distinct seasonal variations, implying the relations of particle sizes and their sources and sinks. The number concentrations of particles in the nuclei mode （10-30 nm）, Aitken mode （30-100 nm）, accumulation mode （100 -1000 nm） and coarse mode （〉1μm） varied in the order of summer 〉 spring 〉 autumn, summer 〉 autumn 〉 spring, autumn 〉 summer 〉 spring, and spring 〉 autumn 〉summer, re- spectively. The diurnal variation of total aerosol number concentrations showed three peaks in all observed periods, which corresponded to two rush hours and the photochemistry period at noon. In general, the NPF in summer occurred under the conditions of east winds and dominant air masses originating from marine areas with high relative humidity （50%-70%） and strong solar radiations （400 -700 W m-2）. In spring, the NPF were generally accompanied by low relative humidity （14%-30%） and strong solar radiations （400-600 W m-2）. The new particle growth rates （GR） were higher in the summertime in the range of 10- 16 nm h-1. In spring, the GR were 6.8-8.3 nm h-1. Under polluted air conditions, NPF events were seldom captured in autumn in Nanjing. During NPF periods, positive correlations between 10- 30 nm particles and 03 were detected, particularly in spring, indicating that NPF can be attributed to photochemical reactions.     

2008年北京奥运会期间大气气溶胶物理特征分析

应用MODIS卫星的气溶胶产品资料和地面的光学粒子计数器的资料,对比分析了北京地区2006、2007、2008年7～9月的气溶胶光学厚度、细粒子光学厚度、Angstrom指数、气溶胶粒子数浓度谱及体积谱,发现2008年北京奥运会期间(7月20日～9月20日)的气溶胶光学厚度比2006、2007年同期明显降低,气溶胶细模态光学厚度占总光学厚度的比上升,Angstrom指数上升,气溶胶细粒子数浓度没有明显相对变化,而粗粒子数浓度则减少约50%.利用大气标高,将MODIS反演的气溶胶柱的质量浓度转化为地面气溶胶质量浓度.用粒子计数器得到的体积谱,在假定气溶胶粒子密度的情况下,计算出其质量浓度.将这两种方法得到的气溶胶质量浓度与国家环境保护部公布的空气质量指数换算得到的可吸入颗粒物(PM10)质量浓度进行比较.结果表明:北京奥运期间空气质量总体达到了国家二级空气质量标准;与2006、2007年同期相比,2008年气溶胶PM10质量浓度明显下降,而这主要是由气溶胶粗粒子的减少引起的.     

Characteristics of mass concentrations depending on synoptic features during airborne dustfall episodes observed at Cheongwon in Korea in 2005

Sandstorms in the desert and loess regions of north China and Mongolia, as well as the associated dustfall episodes on the Korean Peninsula, were monitored in 2005. The ground mass concentrations of PM10 and PM2.5 were analyzed during dustfall episodes at Cheongwon, in central south Korea, based on synoptic features at surface, 850 hPa and 500 hPa levels. A total of seven dustfall episodes lasting eleven days were observed and the mass concentration ratios of PM2.5 and PM10 during dustfall episodes were classified into a severe dustfall episode (SDE) and a moderate dustfall episode (MDE) depending upon two synoptic features. The main synoptic feature was for SDEs, which occurred frequently under a surface anticyclone and cyclone located in the west and east of the Korean Peninsula with large amplitude trough at 500 hPa over the northern Korean Peninsula. The sandstorms at the source headed directly to Korea via a strong N-NW wind without passing through any large cities or industrial areas of east China. The PM10 mass concentration sharply increased during the SDEs; however, the fine aerosol fraction of PM2.5 levels was relatively low with 13.6% of the mass concentration. In a synoptic feature for MDEs, a slow moving cyclone headed to Korea via the industrial areas of northeastern China under a small amplitude trough at a 500 hPa level. A weak anticyclone was also located over China. MDEs showed low mass concentrations of coarse PM10 particles and large fraction of fine PM2.5 particles at 46.3%.     

青藏高原黑碳气溶胶传输及沉降的季节特征模拟分析

根据全球气溶胶气候模式GEM-AQ/EC的1995~2004年模拟,分析了青藏高原大气黑碳气溶胶的来源、传输及沉降季节特征。研究表明:青藏高原黑碳气溶胶主要来自自由对流层和大气边界层的输送。相对于自由对流层的黑碳输送,紧邻青藏高原的南亚、东亚以及东南亚大气边界层的输送更有效,它形成了青藏高原由北向南、自西往东黑碳气溶胶浓度和沉降明显递增的基本分布形态。横跨欧亚大陆自由对流层的黑碳气溶胶由西向东向青藏高原的输送全年不变,夏季输送路径最北但强度最弱,冬季路径最南而强度最强。大气边界层黑碳气溶胶的输送受控于亚洲季风环流变化,来自南亚的黑碳气溶胶在春季越过孟加拉湾传输进入高原东南部,夏季则可翻越喜马拉雅山抵达青藏高原南部腹地;同时我国中部排放的黑碳气溶胶也在东亚夏季风向北扩展中驱动它从东向西往青藏高原东北部传输。从秋季到冬季,随着夏季风撤退,南亚黑碳源区向青藏高原传输衰退,东亚冬季风的反气旋性环流的南侧及西南侧的偏东风携带秋季我国东南部源区和冬季东南亚源区黑碳气溶胶向青藏高原东南部传输。受青藏高原明显的暖湿季和干冷季气候影响,干湿沉降分别主导了青藏高原冬季和夏季黑碳沉降,夏季青藏高原黑碳气溶胶沉降总量大多超过8~10 kg·km-2,在高原东北部的最高值超过40 kg·km-2。冬季青藏高原黑碳气溶胶沉降量最低,大部地区黑碳沉降低于5 kg·km-2。青藏高原黑碳沉降的冬夏季节相差约为2~8倍。     

天津冬季大气能见度与空气污染的相互关系

为探求天津冬季大气能见度特征与空气污染的相互关系,于2008年12月至2009年1月连续观测大气能见度和空气污染物浓度(PM10、PM2.5质量浓度,O_3、NO_2和SO_2体积浓度),并结合相对湿度进行相关分析。结果表明:天津冬季大气能见度平均值为11.59 km,日变化呈明显的单峰特征,其变化特征受到空气污染物,尤其是气溶胶质量浓度及相对湿度变化共同影响;观测期内霾的发生频率接近50%;采用非线性回归方程拟合能见度与气溶胶质量浓度相互关系显示,PM2.5质量浓度对水平能见度的贡献大于PM10质量浓度,并且高湿情况下,能见度与气溶胶质量浓度相关性更好。     

Using Föhn conditions to characterize urban and regional sources of particles

Characterizations of urban and regional sources of particulate matter (PM) were performed in the Milan area (North of Italy) during Föhn and stagnant (non-Föhn) conditions. The measurements were performed at two different places: in an urban area North of Milan (Bresso) and in a regional area at the EMEP-GAW station in Ispra (about 65 km NW from Milan) during the winter periods of the years 2002–2007. Particle size distributions and chemical bulk analysis of aerosols are combined with single particle mass spectrometry to obtain information about the chemical content of the particles and their mixing state. Föhn conditions are characterized by extremely clean background air from which background aerosol is scavenged, and consequently local sources (here defined as sources between the sampling sites and the mountain range top about 100–150 km away depending on the wind direction) determine the aerosol properties.It was observed that during Föhn events the accumulation mode in the size range 50 nm < d < 300 nm practically disappears and that the size fraction below 50 nm dominates the total number distribution. The significant change in the number size distribution and the large decrease in PM10 mass during Föhn events are accompanied by a significant change in the chemical composition of the particles. Results from bulk chemical analysis showed high amounts of carbonaceous compounds and very low concentrations of ammonium nitrate (as indicator for secondary chemistry) during Föhn episodes, in contrast to stagnant conditions, when secondary components are dominating the aerosol composition. Single particle measurements confirm the high contribution of carbonaceous compounds in locally emitted particles.It was concluded that particles that originated in the urban area come mainly from combustion processes, especially direct traffic emissions, domestic heating and industrial activities, whereas the regionally emitted particles are different with much less traffic contribution.We estimate that under prevailing (non-Föhn) winter conditions, about 50–65% of the aerosol mass load in the city of Milan are caused by local emissions, and about 35–50% come from regional background. This finding suggests that in order to improve air quality in a big city like Milan, it is important to combine local traffic restriction interventions with other long-term regional scale air-quality-measures.     

泰山PM10及其中化学成分变化特征

为研究华北平原区域背景气溶胶成分及其变化特征,2010年6月至2011年7月在泰山顶采集了64个PM10滤膜样品,分析了样品的PM10及其中无机盐离子和有机碳（OC）、元素碳（EC）的质量浓度,并对各成分相关性等进行了分析。泰山PM10年均质量浓度约为68.4 mg/m³,其中无机盐离子约占总质量的64.8%,碳气溶胶约占17.4%。无机盐离子的质量浓度从春季逐渐增大,夏季达到峰值,秋季下降,冬季最小;OC质量浓度从春季至秋季逐渐增高,冬季最低,EC变化类似,但夏秋两季差别不大。二次有机碳（SOC）与OC的比值四季均在50%以上,年均值约为58.5%。通过后向轨迹聚类分析发现,在经过城市的较短轨迹以及南方较短混合轨迹的影响下,泰山PM10质量浓度较高,而西北长距离传输气团PM10浓度均较低。     

山西省PM_(10)气溶胶污染特征分析

文章针对大同市2006—2009年、榆社县2006—2008年PM10质量浓度数据,使用趋势分析、后向轨迹模拟不同高度的PM10的传输路径,可以看出:PM10浓度的日变化特征为"两高三低";PM10浓度日际变化不明显,只在典型日PM10浓度值明显增大;PM10浓度月变化特征为1、5、12月浓度高,春季5月份由于为沙尘期浓度高。PM10浓度季节变化规律与采暖期和非采暖期变化相符合,即采暖期的冬春季浓度高、非采暖期的夏秋季浓度低;从2006—2009年间,两站PM10质量浓度基本呈逐年下降趋势。不同气象要素与PM10浓度的相关性,按相关系数绝对值从大到小排列依次为:露点温度、气温、降水量、相对湿度。其中露点温度和PM10浓度呈显著负相关性,气温与PM10浓度呈较弱负相关性。     

Study on Size Distributions of Airborne Particles by Aircraft Observation in Spring over Eastern Coastal Areas of China

The authors studied the size distributions of particles at an altitude of 2000 m by aircraft observation over eastern costal areas of China from Zhuhai, Guangdong to Dalian, Liaoning (0.3,7-30μm, 57 channels,including number concentration distribution, surface area concentration distribution and mass concentration distribution). In these cities, the average daily concentrations of PM10 are very high. They are among the most heavily polluted cities in China. The main pollution sources are anthropogenic activities such as wood, coal and oil burning. The observed size distributions show a broad spectrum and unique multi-peak characteristics, indicating no significant impacts of individual sources from urban areas. These results are far different from the distribution type at ground level. It may reflect the comprehensive effect of the regional pollution characteristics. Monitoring results over big cities could to some extent reflect their pollution characteristics.     

A study of aerosol properties over Lahore (Pakistan) by using AERONET data

It is well established that aerosols affect the climate in a variety of ways. In order to understand these effects, we require an insight into the properties of aerosols. In this paper we present a study of aerosol properties such as aerosol optical depth (AOD), single scattering albedo (SSA) and aerosol radiative forcing (ARF) over mega city of Lahore (Pakistan). The data from Aerosol Robotic Network (AERONET) have been used for the period December 2009 to October 2011. The seasonal average values of AOD, asymmetry parameter (ASY) and volume size distribution in coarse mode were observed to be highest in summer. On the other hand, the average values of Angstrom exponent (AE) and imaginary part of refractive index (RI) were found to be maximum in winter. The average value of real part of RI was found to be higher in spring than in all other seasons. The SSA exhibited an increasing trend with wavelength in the range 440 nm–1020 nm in spring, summer and fall indicating the dominance of coarse particles (usually dust). However, a decreasing trend was found in winter in the range 675 nm–1020 nm pointing towards the dominance of biomass and urban/industrial aerosols. As far as aerosol radiative forcing (ARF) is concerned, we have found that during the spring season ARF was lowest at the surface of Earth and highest at top of the atmosphere (TOA). This indicates that the atmosphere was warmer in spring than in all the remaining seasons.     

北京市大气细粒子的质量浓度特征研究

大气能见度的降低是当今国际上比较突出的城市环境问题。北京近年的监测结果表明 ,大气中通过消光作用使大气能见度下降的气溶胶细粒子的污染程度呈现上升趋势。从 2 0 0 1年对北京市气溶胶细粒子 (空气动力学直径小于 2 .5μm的粒子 ) 4个季节的采样监测结果分析 (有效采样天数为 50d)得出 ,北京市细粒子质量浓度年平均值已超过美国国家标准的 7倍以上。研究发现细粒子的质量浓度不仅与环境条件有关 ,而且与气象条件也有着密切的关系。文中以细粒子的观测数据为基础 ,结合当时的气象条件进行细粒子浓度与气象条件定量关系的研究     

金沙区域可吸入颗粒物浓度及其与气象因子的相关分析

选用咸宁市金沙区域2006年6月至2007年5月可吸入颗粒物质量浓度监测资料,分析了金沙颗粒物质量浓度时间分布特征。分析结果表明：金沙三种可吸入颗粒物PM10、PM2.5、PM1.0质量浓度变化规律基本一致,年季变化表现为秋冬大,夏春小;日变化呈双峰双谷型周期性变化,白天大于夜间,最大值出现在下午16-19时,最小值出现在清晨03-07时,除秋季外第二峰谷表现不明显。且雨雾天气PM10浓度较晴到多云低。且通过与2006年6月至2007年5月的地面气象要素资料相关分析,发现PM10质量浓度与气温、气压呈显著正相关,与降水、风速、湿度呈显著负相关。     

Large aerosol particles in cirrus type clouds

Research flights in November 1990 over the central parts of the United States, Wyoming and Colorado, were aimed to the investigation of the properties and microstructure of cirrus clouds (mainly cirrocumulus lenticularis). Among the other parameters measured on board the NCAR Saberliner were the concentration and size distribution of submicron particles and, in some cases, the particle deliquescence. For coarse insoluble particles found inside and outside of cloud elements, size distributions and morphology information were obtained by evaluating inertial impactor samples with an optical microscope and scanning electron microscope. In addition, the coarse particle composition was determined by x-ray energy spectrum analysis. The following conclusions from these measurements are:The large and coarse particle size distribution can be roughly simulated by a log-normal function with the modus around r=0.5 μm. Particle concentrations are very variable between several tenths and several particles per cm³. Particle volume distribution features a distinct maximum around 0.75 μm without a broad plateau which was observed in the case of sampling at lower altitude. Aerosol composition heterogeneity at cirrus cloud level is well documented by the evaluation of the fine particle sampling taken with the UMR sampling system. This heterogeneity can be partly explained by the interaction between aerosol and cloud elements, which is documented by the measured particle size distribution curves inside and outside of cloud elements. Assuming that particle deliquescence is caused by H₂SO₄ and/or by (NH₄)₂SO₄, particle soluble mass fractions were found to be around 30% in the first case and about 40% in the second. The most frequently occurring elements in large and coarse particles at cirrus cloud level were Si, Cl, Ba, S, Ca and C.