霾期间上海低层气溶胶微物理属性与地面相对湿度分析

用2007年1月至2010年11月美国国家航空航天局(NASA)的CALIPSO星载激光雷达资料,通过532 nm总后向散射系数、体积退偏比和色比,分析了上海地区霾期间低层0~2 km高度气溶胶微物理属性与地面相对湿度的关系。结果表明,当地面相对湿度为65%~80%时,后向散射系数在0~0.001 km-1·sr-1范围内出现的频率最大;当地面相对湿度为50%~65%时,后向散射系数大于0.001 km-1·sr-1的频率最大;低层大气中聚集的主要是规则气溶胶粒子,当地面相对湿度为65%~80%时,气溶胶粒子最为规则,其次为80%~95%的地面相对湿度。当地面相对湿度为50%~65%时,不规则气溶胶粒子所占比重较大;霾期间,低层大气中细粒子气溶胶均占主导地位,但随着地面相对湿度的增大,气溶胶粒子粒径逐渐增大。在地面相对湿度为80%~95%时,大颗粒气溶胶相对较多。     

Scattering Properties of Atmospheric Aerosols over Lanzhou City and Applications Using an Integrating Nephelometer

The data, measured by a three-wavelength Integrating Nephelometer over Lanzhou City during the winters of 2001/2002 and 2002/2003 respectively, have been analyzed for investigating the scattering properties of atmospheric aerosols and exploring their relationship and the status of air pollution. The aerosol particle volume distribution is inverted with the measured spectral scattering coefficients. The results show that the daily variation of the aerosol scattering coefficients is in a tri-peak shape. The average ratio of backscattering coefficient to total scattering coefficient at 550 nm is 0.158; there exists an excellent correlation between the scattering coefficients and the concentration of PM10. The average ratio of the concentration of PM10 to the scattering coefficients is 0.37 g m-2, which is contingent on the optical parameters of aerosol particles such as the size distribution, etc.; an algorithm is developed for inverting the volume distribution of aerosol particles by using the histogram and Monte-Carlo techniques, and the test results show that the inversion is reasonable.     

Characteristics and source of black carbon aerosols at Akedala station, Central Asia

Black carbon concentration and weather data were online monitored continuously from March 2008 to February 2009 at the Akedala regional atmosphere station in the arid region of Central Asia. We present the daily, monthly and seasonal variations of BC concentration in the atmosphere and discuss the possible emission sources. Black carbon concentration in this region varies in the range of 43.7–1,559.2?ng/m³. A remarkable seasonal variation of BC in the aerosol was observed in the order of winter?>?spring?>?autumn?>?summer. The peak value of BC appeared at 10:00–13:00 while the lowest one at 7:00–9:00 each day. Air masses backward trajectories show the potential emission sources in the northwest from spring to autumn. Through back trajectory also revealed that BC in winter might be attributed to the emission from the anthropogenic activities, including domestic heating, cooking, combustion of oil and natural gas, and the medium-range transport from those cities in northern slope of Tianshan Mountains and Siberia. Some BC aerosols from the arid region of Central Asia were transported to the Pacific Ocean by the Westerlies.     

Scattering and absorption coefficients of aerosols in a semi-arid area in China: Diurnal cycle, seasonal variability and dust events

The authors investigated variations of aerosol scattering and absorptive properties in a semi-arid climate Observatory in the Inner Mongolia of China and factors affecting the variation. They use integrated nephelometer and aethalometer observations collected in 2005 and 2006 at the Silinhot Observatory. The results are as follows. 1) in autumn and winter, the diurnal cycle of scattering coefficient exhibited a clear bi-modal variation, and the scattering coefficient was indicative of the type of sandy weather. 2) The concentration of black carbon (BC) aerosols was much higher in winter than in the other seasons with an evident bimodal diurnal variation. 3) When the wind speed was lower than 3.5 m s^?1, the dilution effect of air evidently influenced the scattering coefficient and BC mass concentration; for the wind speed above 3.5 m s^?1, there appeared to be little correlation between wind speed and scattering coefficient or BC mass concentration. 4) Atmospheric visibility calculated from the aerosol scattering and absorptive coefficients was in good agreement with the direct observation of visibility. 5) Absorption by aerosols accounted for 25% of the total extinction in December.     

基于CALIPSO卫星资料的华东地区气溶胶垂直分布特征

基于2010年12月1日—2011年11月30日美国国家航空航天局云—气溶胶激光雷达与红外探测者卫星搭载的激光雷达CALIPSO的监测数据,通过分析消光后向散射系数、体积退偏比和色比,得到了华东地区垂直方向上气溶胶粒子的散射能力、尺度、规则程度随高度的变化及其季节变化特征。结果表明:随着高度的增加华东地区大气的散射能力减弱。整层大气不同季节粒子的形状大小不同,春季不规则、大粒径粒子所占比例与其他季节相比较大。夏季较规则、小粒径的粒子较多。各高度层的后向散射系数值分布范围为5×10-4~20×10-4 km-1·sr-1。对不同高度消光后向散射系数、体积退偏比和色比随时间变化的研究表明,春季受沙尘输送的影响,0~4 km大气层中不规则大粒径粒子较多;4~8 km大气层由于所含气溶胶粒子较少,大气散射能力随季节变化不明显;而8~10 km大气层中粒子含量最少,导致大粒径粒子所占比例较高,此外该高度层在秋季不规则、大粒径粒子相对较多,冬季规则、小粒径粒子相对较多。     

Aerosol physical characteristics at Bhubaneswar, East coast of India

Physical characterization of atmospheric aerosols was carried out using various equipments like Grimm's spectrophotometer, Aetholometer and Microtops-II at Bhubaneswar, a coastal city in the east coast of India. Meteorological parameters were recorded on-line with an automatic weather station, which showed weather relatively free from extreme events with high humidity during the period. The pre-monsoon months showed an increase in aerosol mass in the higher size ranges. The black carbon (BC) showed maximum values during winter which may be due to various anthropogenic activities like biomass burning and forest fire as well as dry conditions conducive to transport from far off places. The α values representing aerosol size distribution and β values showing the total aerosol concentration in vertical air column rose simultaneously in pre-monsoon months to attain maximum values during February–March 2008. The AOD was also correlated with PM-10 and BC concentrations.     

天津市区秋冬季大气气溶胶散射系数的变化特征

通过对天津市区2006年9月至2007年2月期间散射系数进行统计分析,得出天津市区秋冬季气溶胶散射系数特征：散射系数小时平均值变化范围在100～10000 Mm~（-1）,日变化呈典型双峰形,峰值出现在早6时和晚22时,散射系数分别为508.5和431.4 Mm。冬季散射系数要高于秋季。雾日、霾日和晴天时的平均散射系数分别为588.8,403.7和172.5Mm,雾日的散射系数最大,晴天的散射系数最小。细粒子PM_（2.5）浓度日变化与散射系数日变化曲线非常接近,两者呈正相关,相关系数达到0.78。出现大风扬沙天气时散射系数变化剧烈,PM_（10）浓度出现高值,而散射系数却降低,扬沙天气导致空气中的大粒子浓度增加,当PM_（10）质量浓度表现为高值时,散射系数并没有表现为高值。     

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.     

山西夏季气溶胶散射特征的飞机观测研究

利用3个架次的积分浊度仪和PCASP-100X（Passive Cavity Aerosol Spectrometer Probe）机载观测资料,分析了2013年山西夏季空中有云、无云和少云3种不同条件下气溶胶散射系数的分布特征,讨论了气溶胶散射系数垂直变化与气溶胶数浓度、气象条件的关系,并结合HYSPLIT（Hybrid of Single Particle Lagrangian Integrated Trajectory model）后向轨迹模型研究气溶胶的运动轨迹和可能的污染来源。结果表明:山西夏季空中气溶胶总散射系数变化范围为0～499 Mm-1,晴空气溶胶数浓度和总散射系数明显大于有云和少云时。气溶胶总散射系数一般随高度的增加而递减。造成气溶胶总散射系数、数浓度偏高的原因有下垫面污染源多、风速小、相对湿度高以及逆温层的存在。550 nm波段气溶胶后向散射比大于0.1,粒径0.1～0.5 μm的气溶胶粒子对散射影响最大,说明山西空中细粒子污染比较严重。气溶胶总散射系数与数浓度有一定的相关性。引起气溶胶总散射系数、数浓度较高的气团传输路径主要为西南路径,局地排放的气溶胶大于远距离传输的气溶胶对散射系数的贡献。     

Scattering Properties of Atmospheric Aerosols over Lanzhou City and Applications Using an Integrating Nephelometer

The data, measured by a three-wavelength Integrating Nephelometer over Lanzhou City during the winters of 2001/2002 and 2002/2003 respectively, have been analyzed for investigating the scattering properties of atmospheric aerosols and exploring their relationship and the status of air pollution. The aerosol particle volume distribution is inverted with the measured spectral scattering coefficients. The results show that the daily variation of the aerosol scattering coefficients is in a tri-peak shape. The average ratio of backscattering coefficient to total scattering coefficient at 550 nm is 0.158; there exists an excellent correlation between the scattering coefficients and the concentration of PM10. The average ratio of the concentration of PM10 to the scattering coefficients is 0.37g m^-2, which is contingent on the optical parameters of aerosol particles such as the size distribution, etc.; an algorithm is developed for inverting the volume distribution of aerosol particles by using the histogram and Monte-Carlo techniques, and the test results show that the inversion is reasonable.     

Connection between ozone concentration and atmosphere circulation at peak Moussala

Connection between ozone concentration and atmosphere circulation is investigated based on measurements at BEO station, peak Moussala (2,925 m a.s.l.), for the period 09 August 2006 to 29 January 2008. Ozone concentration data are collected with UV-analyzer “Environnement O₃ 42” and meteo data with weather station “Vaisala”. There are measurements of ⁷Be. Data from NOAA HYSPLIT model for particle trajectories are also used. Eight wind directions and three ranges of wind velocities are employed in the analysis. A comparison of ozone concentrations in upward and downward air transport according to HYSPLIT model is made. The number of cases with ozone concentration above 63 ppb has been counted. Mann–Whitney nonparametric test is employed as a basic statistical method. Correlation between atmosphere pressure and tropospheric ozone content is made. The same is done for ⁷Be and ozone. The main conclusion is that there is not any local or regional pollution effect detectable at peak Moussala, but most of the ozone measured is due to emissions of hydrocarbons and NO _x over a larger region. There could be some regional sources of ozone building substances in southwest direction from peak Moussala. Air transported from the north quarter has higher ozone concentrations compared to the south quarter. In vertical direction, upward transport of air masses shows higher values of ozone concentration. Higher wind velocity is associated with low ozone concentrations at peak Moussala. The annual course of ozone concentration has summer maximum and winter minimum. There is right connection between air pressure and ozone concentration. The same is valid for the correlation between ⁷Be and ozone. Diurnal ozone course shows daytime maximum in winter and nighttime maximum in summer.     

Chemical Composition of Summertime PM2.5 and Its Relationship to Aerosol Optical Properties in Guangzhou, China

Urban aerosols have a large effect on the deterioration of air quality and the degradation of atmospheric visibility.Characterization of the chemical composition of PM 2.5 and in situ measurements of the optical properties of aerosols were conducted in July 2008 at an urban site in Guangzhou,Southern China.The mean PM 2.5 concentration for the entire period was 53.7±23.2 μg m 3.The mean PM 2.5 concentration (82.7±25.4 μg m 3) on hazy days was roughly two times higher than that on clear days (38.8±8.7 μg m 3).The total water-soluble ion species and the total average carbon accounted for 47.9%±4.3% and 35.2%±4.5%,respectively,of the major components of PM 2.5.The increase of secondary and carbonaceous aerosols,in particular ammonium sulfate,played an important role in the formation of haze pollution.The mean absorption and scattering coefficients and the single scattering albedo over the whole period were 53±20 M m 1,226±111 M m 1,and 0.80±0.04,respectively.PM 2.5 had a high linear correlation with the aerosol extinction coefficient,elemental carbon (EC) was correlated with aerosol absorption,and organic carbon (OC) and SO 4 2 were tightly linked to aerosol scattering.     

沈阳冬夏季可吸入颗粒物浓度及尺度谱分布特征

利用沈阳大气成分监测站颗粒物监测仪 (Grimm 180) 连续测得的夏季 (2006年8月)、冬季 (2006年12月和2007年1月) 可吸入颗粒物的数浓度和质量浓度数据, 分析了沈阳市可吸入颗粒物浓度日变化、谱分布及污染特征, 在此基础上结合沈阳市常规气象资料, 分析了气象要素和颗粒物污染之间的关系。结果表明:沈阳市冬、夏季部分时段可吸入颗粒物浓度存在明显的日变化和日际变化; 谱分布较好地符合Junge分布; 沈阳冬季PM₁₀超标日数占冬季观测总天数的77%, PM_2.5超标日数 (按美国EPA日均标准) 占冬季观测总天数的87%, PM₁₀平均数浓度为6668.7个/cm3, 平均质量浓度达252.8μg/m3, 分别是夏季的3.0和2.4倍; 冬、夏季PM_2.5/PM₁₀平均质量分数分别为0.647和0.603, PM_2.5占可吸入颗粒物总数量的99%以上; 浓度变化在很大程度上受到各种气象要素的影响, 与温度、风速负相关, 与湿度正相关, 降雨、降雪过程使得颗粒物浓度明显降低, 近地层逆温和雾是颗粒物增多的一个重要因素。颗粒物污染对城市能见度影响较大。     

南京北郊2011年春季气溶胶粒子的散射特征

利用南京北郊2011年春季积分浊度仪的观测资料,结合PM_2.5质量浓度、能见度和常规气象资料,分析了南京北郊春季气溶胶散射系数的变化特征、散射系数与PM_2.5质量浓度和能见度的关系。结果表明,观测期间气溶胶散射系数平均值为311.5±173.3 Mm^-1,小时平均值出现频率最高的区间为100~200 Mm^-1;散射系数的日变化特征明显,总体为早晚大,中午及午后小。散射系数与PM_2.5质量浓度的变化趋势基本一致,但与能见度呈负相关关系。霾天气期间散射系数日平均值为700.5±341.4 Mm^-1,最高值达到近1 900 Mm^-1;结合地面观测资料、NCEP/NCAR再分析资料和后向轨迹模式分析显示,霾期间气块主要来自南京南部和东南方向。     

THE DIRECT EFFECTS OF AEROSOLS AND DECADAL VARIATION OF GLOBAL SEA SURFACE TEMPERATURE ON THE EAST ASIAN SUMMER PRECIPITATION IN CAM3.0

Using the CAM3.0 model, we investigated the respective effects of aerosol concentration increasing and decadal variation of global sea surface temperature(SST) around year 1976/77 on the East Asian precipitation in boreal summer. By doubling the concentration of the sulfate aerosol and black carbon aerosol separately and synchronously in East Asia(100-150 °E, 20-50 °N), the climate effects of these aerosols are specifically investigated. The results show that both the decadal SST changing and aerosol concentration increasing could lead to rainfall decreasing in the center of East Asia, but increasing in the regions along southeast coast areas of China. However, the different patterns of rainfall over ocean and lower wind field over Asian continent between aerosol experiments and SST experiments in CAM3.0 indicate the presence of different mechanisms. In the increased aerosol concentration experiments, scattering effect is the main climate effect for both sulfate and black carbon aerosols in the Eastern Asian summer. Especially in the increased sulfate aerosol concentration experiment, the climate scattering effect of aerosol leads to the most significant temperature decreasing, sinking convection anomalies and decreased rainfall in the troposphere over the central part of East Asia. However, in an increased black carbon aerosol concentration experiment, weakened sinking convection anomalies exist at the southerly position. This weakened sinking and its compensating rising convection anomalies in the south lead to the heavy rainfall over southeast coast areas of China. When concentrations of both sulfate and black carbon aerosols increase synchronously, the anomalous rainfall distribution is somewhat like that in the increased black carbon concentration aerosol experiment but with less intensity.     

东亚地区人为气溶胶直接辐射强迫及其气候效应的数值模拟

利用耦合化学过程的区域气候模式RegCM3,模拟研究3种主要人为排放气溶胶(硫酸盐、黑碳、有机碳)对东亚区域气候的影响.计算分析近20 a来3种气溶胶的时空分布、综合辐射强迫作用及其对地面气温和降水的影响.模拟结果表明:3种气溶胶冬夏季分布有所不同,冬季气溶胶大值区主要分布在南方地区,而夏季大值区北移;气溶胶短波辐射强迫在大气层顶和地面均为负值;气溶胶的加入对东亚地区地表气温有明显影响,冬季降温中心位于四川盆地,夏季降温大值区位于华北地区.气溶胶直接气候效应使得冬季东亚大部分地区降水减少,夏季东亚地区降水与中国南方地区夏季气溶胶浓度有较好的相关关系,中国东部雨带有南移趋势.     

塔克拉玛干沙漠与撒哈拉沙漠沙尘气溶胶光学特性对比研究

基于2007—2021年CALIPSO和MODIS主、被动卫星遥感探测数据,对塔克拉玛干沙漠和撒哈拉沙漠的气溶胶光学特性时空分布特征进行探究及对比分析。结果表明：（1）两大沙漠的沙尘气溶胶对总气溶胶的贡献率最大,气溶胶类型季节变化的相对单一性反映了塔克拉玛干沙漠和撒哈拉沙漠地区存在沙漠沙尘排放对总气溶胶成分的显著影响;（2）塔克拉玛干沙漠气溶胶光学厚度AOD的峰值出现在春季（春季>夏季>秋季>冬季）,而撒哈拉沙漠AOD的峰值出现在夏季（夏季>春季>秋季>冬季）;（3）撒哈拉沙漠总气溶胶抬升高度与塔克拉玛干沙漠相近,但近地面层消光系数明显小于塔克拉玛干沙漠;塔克拉玛干沙漠的消光系数平均值在所有季节中均大于撒哈拉沙漠,故塔克拉玛干沙漠的沙尘气溶胶AOD比撒哈拉沙漠的大;相比沙漠沙尘气溶胶,塔克拉玛干沙漠和撒哈拉沙漠都无明显的污染沙尘和抬升烟活动。上述研究结果揭示了两大沙漠源区沙尘气溶胶光学特性的观测事实与利用大气气溶胶时空变化特征反映区域气候变化的可能性。     

Observed changes in aerosol physical and optical properties before and after precipitation events

Precipitation scavenging of aerosol particles is an important removal process in the atmosphere that can change aerosol physical and optical properties. This paper analyzes the changes in aerosol physical and optical properties before and after four rain events using in situ observations of mass concentration, number concentration, particle size distribution, scattering and absorption coefficients of aerosols in June and July 2013 at the Xianghe comprehensive atmospheric observation station in China. The results show the effect of rain scavenging is related to the rain intensity and duration, the wind speed and direction. During the rain events, the temporal variation of aerosol number concentration was consistent with the variation in mass concentration, but their size-resolved scavenging ratios were different. After the rain events, the increase in aerosol mass concentration began with an increase in particles with diameter 0.8 μm [measured using an aerodynamic particle sizer(APS)], and fine particles with diameter 0.1 μm [measured using a scanning mobility particle sizer(SMPS)]. Rainfall was most efficient at removing particles with diameter ～0.6 μm and greater than 3.5 μm. The changes in peak values of the particle number distribution(measured using the SMPS) before and after the rain events reflect the strong scavenging effect on particles within the 100–120 nm size range. The variation patterns of aerosol scattering and absorption coefficients before and after the rain events were similar, but their scavenging ratios differed, which may have been related to the aerosol particle size distribution and chemical composition.     

华北中部夏季气溶胶和云分布特征

气溶胶与云的垂直分布特征是气溶胶间接气候效应关注的重点。基于2018年7—8月华北中部6架次飞机观测数据,研究气溶胶和云滴的垂直和水平分布特征。结果表明:华北中部780~5687 m高度内气溶胶数浓度( N_a )平均值为821.36 cm-3,最大量级可达到104 cm-3,云中气溶胶数浓度(N_acc)占总颗粒浓度的80%以上,表明细颗粒占大多数,气溶胶粒子算术平均直径( D_m )平均值为0.12~0.52 μm;大气层结对气溶胶垂直分布影响较大,逆温阻挡气溶胶垂直输送,高空(高度2000 m以上) D_m 的垂直分布受到相对湿度影响较大; N_a 和 D_m 在垂直方向波动较大,水平方向波动较小;低层云中云滴数浓度(N_c)较大、液态水含量(L)较小,而中层和高层云中N_c较小、L较大,N_c和云滴有效半径(R_e)的概率密度函数均为双峰型分布,L的概率密度函数为单峰型分布;气溶胶数浓度谱基本呈现多峰型分布,而云滴数浓度谱多呈现单峰型分布。     

Comparison of Two Air Pollution Episodes over Northeast China in Winter 2016/17 Using Ground-Based Lidar

This study analyzes and compares aerosol properties and meteorological conditions during two air pollution episodes in 19–22 (E1) and 25–26 (E2) December 2016 in Northeast China. The visibility, particulate matter (PM) mass concentration, and surface meteorological observations were examined, together with the planetary boundary layer (PBL) properties and vertical profiles of aerosol extinction coefficient and volume depolarization ratio that were measured by a ground-based lidar in Shenyang of Liaoning Province, China during December 2016–January 2017. Results suggest that the low PBL height led to poor pollution dilution in E1, while the high PBL accompanied by low visibility in E2 might have been due to cross-regional and vertical air transmission. The PM mass concentration decreased as the PBL height increased in E1 while these two variables were positively correlated in E2. The enhanced winds in E2 diffused the pollutants and contributed largely to the aerosol transport. Strong temperature inversion in E1 resulted in increased PM_2.5 and PM₁₀ concentrations, and the winds in E2 favoured the southwesterly transport of aerosols from the North China Plain into the region surrounding Shenyang. The large extinction coefficient was partially attributed to the local pollution under the low PBL with high ground-surface PM mass concentrations in E1, whereas the cross-regional transport of aerosols within a high PBL and the low PM mass concentration near the ground in E2 were associated with severe aerosol extinction at high altitudes. These results may facilitate better understanding of the vertical distribution of aerosol properties during winter pollution events in Northeast China.