Remote and in situ measurements of aerosol concentration in the Arctic troposphere from the Yak-42D “Roshydromet” research aircraft

The results are presented of measurements of aerosol content at different heights in the Arctic troposphere in the area of Naryan-Mar city and the Yamal Peninsula on June 24, 2014 using in situ and remote instruments installed on the Yak-42D "Roshydromet" research aircraft. The maximum aerosol content was detected in the layer up to 3000 m, and the aerosol concentration in the troposphere over the Yamal Peninsula is higher than that in the area of Naryan-Mar by 100 times. The in situ aircraft instrument measured the number concentration of black carbon particles in the tropospheric aerosol. To identify the sources of aerosol in the Arctic troposphere during airborne measurements the air mass trajectory analysis was performed. Simulations were conducted using the TRACAO trajectory model and FLEXPART particle dispersion model. The possible contribution of long-range and local transport of industrial pollutants to the Arctic troposphere was analyzed. The air mass transport was simulated using the trajectory model. Model computations of aerosol concentration in the troposphere using the satellite data on the gas flaring incite that the high content of black carbon in the lower troposphere over the Yamal Peninsula was caused by its transfer from the oil-producing areas located on the adjoining territory of Russia. The contribution of long-range transport of pollutants from industrial enterprises in Western Europe to the Arctic area under study was insignificant in the period under consideration.     

1984～2000年印度洋与中国地区上空对流层中上层及平流层气溶胶变化和输送特征

利用美国SAGE II (Stratospheric Aerosol and Gas Experiment II)卫星最新版（6.0版）1.020 μm通道逐日气溶胶消光系数资料，得出了对流层中上层及平流层（10 km以上高度）气溶胶光学厚度的平均分布和变化特征。结果表明:气溶胶光学厚度在低纬度大，在印度洋的岛屿上空有三个高值中心，气溶胶光学厚度高值中心与对流层中上层的上升气流的高值中心相对应。与17年(1984～2000年)年平均相比，近6年（1995～2000年）孟加拉湾至青藏高原东南部上空气溶胶光学厚度明显增加；中国东部地区上空气溶胶光学厚度增加，中西部地区则减小。气溶胶光学厚度存在三个经向的增加带和两个经向的减小带。中纬度与赤道之间的布鲁尔-多普森环流（Brewer-Dobson Circulation）带来的低层大气与对流层中上层及平流层之间的气溶胶输送是导致气溶胶这种经向一致变化的主要因素。气溶胶的这种输送产生的近地面大气污染物向中上层大气输送有可能产生重要的气候变化。     

Studies of ice nucleation by Arctic aerosol on AGASP-II

Aerosol particles were collected on filters for studies of their ability to nucleate ice during the second Arctic Gas and Aerosol Sampling Program (AGASP-II) in April, 1986. The ice nuclei (IN) samples were collected from an aircraft at altitudes ranging from the surface to the vicinity of the tropopause in Arctic locations over Alaska, northern Canada and Greenland. Samples of other components of the aerosol were collected and measurements were made of other properties of the aerosol coincident in time with the IN samples. The IN filters were exposed to water saturation in a dynamic developing chamber at –15° C and –25° C. Ice crystals grew on the IN and were counted on the filters at discrete time intervals during the exposure period to determine the rate of ice nucleation and the final concentration of (IN). Results show that Arctic haze aerosol, identified by pollutant signatures, had lower IN concentrations, a lower IN to total aerosol fraction and slower ice nucleation rates than aerosol which had a chemical signature more indicative of the remote unpolluted troposphere. These observations suggest that the Arctic haze aerosol does not efficiently form ice in the arctic troposphere. This may be a factor contributing to the long-range transport of Arctic haze.     

利用MODIS卫星资料对中国中东部和印度次大陆气溶胶特性的分析

利用Terra和Aqua卫星上的MODIS探测反演气溶胶产品,比较分析了中国中东部和印度次大陆地区的气溶胶物理特性的异同。研究结果表明:中国中东部气溶胶类型以烟尘为主,印度次大陆地区东、西部分别以烟尘和沙尘为主。两地气溶胶光学厚度均有明显的年际变化,冬季低,夏季高。在夏季,两地烟尘所占比例都很大,且光学厚度也大,故两地污染状况都比较严重。总体来说,中国中东部地区污染程度要高于印度次大陆地区。     

Application of particle induced X-ray emission to aerosol long-range transport studies—transport pathways of pollution aerosol over the Atlantic ocean and Europe

Particle induced X-ray emission analysis (PIXE) has been applied to aerosol long-range transport studies. The combination of a size fractionating sampler and a multi-element technique has enabled the identification of the transport pathways of individual constituents over the Atlantic Ocean and Europe. Chemical and size distribution data were obtained for aerosols collected at different sampling sites for the ground layer and the free atmosphere. Evaluation of these data under the aspect of air mass history extended the elemental determination in long range transport. A statistical technique was introduced and used to succeed in the semi-quantitative determination of transported pollutants.     

Airborne Observations of Cloud Condensation Nuclei Spectra and Aerosols over East Inner Mongolia

A set of vertical profiles of aerosol number concentrations, size distributions and cloud condensation nuclei(CCN)spectra was observed using a passive cloud and aerosol spectrometer(PCASP) and cloud condensation nuclei counter, over the Tongliao area, East Inner Mongolia, China. The results showed that the average aerosol number concentration in this region was much lower than that in heavily polluted areas. Monthly average aerosol number concentrations within the boundary layer reached a maximum in May and a minimum in September, and the variations in CCN number concentrations at different supersaturations showed the same trend. The parameters c and k of the empirical function N = c S~kwere 539 and1.477 under clean conditions, and their counterparts under polluted conditions were 1615 and 1.42. Measurements from the airborne probe mounted on a Yun-12(Y12) aircraft, together with Hybrid Single-Particle Lagrangian Integrated Trajectory model backward trajectories indicated that the air mass from the south of Tongliao contained a high concentration of aerosol particles(1000–2500 cm~(-3)) in the middle and lower parts of the troposphere. Moreover, detailed intercomparison of data obtained on two days in 2010 indicated that the activation efficiency in terms of the ratio of NCCNto N_a(aerosols measured from PCASP) was 0.74(0.4 supersaturations) when the air mass mainly came from south of Tongliao, and this value increased to 0.83 on the relatively cleaner day. Thus, long-range transport of anthropogenic pollutants from heavily polluted mega cities,such as Beijing and Tianjin, may result in slightly decreasing activation efficiencies.     

生物质燃烧输送对青藏高原气溶胶光学辐射特性的影响研究

利用青藏高原拉萨(Lhasa)和珠峰(QOMS_CAS)站点地基CE 318太阳光度计观测数据,研究了2012年4月2日至4月5日一次生物质燃烧输送对青藏高原气溶胶光学和辐射特性的影响;并结合卫星遥感产品以及后向轨迹模式分析了本次生物质燃烧输送的可能来源。结果表明：本次气溶胶污染期间Lhasa和QOMS_CAS站点的主要气溶胶类型变为生物质燃烧气溶胶,气溶胶粒子的消光性增大(气溶胶光学厚度(AOD)增大,Lhasa和QOMS_CAS站点AOD最大值分别为0.4和0.29),尺度减小(消光波长指数(EAE)>1.5),吸收性增大(吸收波长指数(AAE)>1.3),细模态粒子体积浓度增大,而细模态粒子峰值半径减小。气溶胶辐射强迫表明此次输送过程使得Lhasa和QOMS_CAS站点的气溶胶对大气顶和地表的降温作用增强,对大气的增温作用也增强。生物质燃烧输送的可能来源为南亚的印度东北部,尼泊尔与不丹地区。     

Characteristics of atmospheric aerosol during the anomalous fall of 2005 in the Moscow region

Results are presented of measurements of total concentration and size spectrum of aerosol particles, of ice nuclei, and cloud condensation nuclei concentrations, as obtained during an anomalously arid period in September and October 2005 in the town of Dolgoprudny, Moscow oblast. It is shown that a two-month period of anticyclonic weather, associated with peat fires, caused a 1.5-time increase in the mean number concentration of aerosol at the site. Effects of accumulation of the industrial aerosol from Moscow and of peat bog burning products are different on fractions of particles of different sizes and on cloud-active nuclei. The smoke particles increased concentrations of almost all sizes from 0.042 to 10 μm; urban aerosol makes the greater part of concentration of particles in the middle subm-icron range and causes a significant increase in the concentration of cloud condensation nuclei.     

青藏高原五道梁低层大气气溶胶来源的初步分析：Ⅱ.源地和输送

基于对五道梁大气气溶胶来源的分析结果和青藏高原及其附近地区环流和天气特征，根据各源气溶胶的浓度变化与单站气象要素变化的关系，讨论了气溶胶的源区和输送。五道梁有两个稳定的污染排放源，全年均对该地低层大气有影响。     

Optical and radiative properties of aerosols during a severe haze episode over the North China Plain in December 2016

The optical and radiative properties of aerosols during a severe haze episode from 15 to 22 December 2016 over Beijing, Shijiazhuang, and Jiaozuo in the North China Plain were analyzed based on the ground-based and satellite data, meteorological observations, and atmospheric environmental monitoring data. The aerosol optical depth at 500 nm was < 0.30 and increased to > 1.4 as the haze pollution developed. The Ångström exponent was > 0.80 for most of the study period. The daily single-scattering albedo was > 0.85 over all of the North China Plain on the most polluted days and was > 0.97 on some particular days. The volumes of fine and coarse mode particles during the haze event were approximately 0.05–0.21 and 0.01–0.43 μm³, respectively—that is, larger than those in the time without haze. The daily absorption aerosol optical depth was about 0.01–0.11 in Beijing, 0.01–0.13 in Shijiazhuang, and 0.01–0.04 in Jiaozuo, and the average absorption Ångström exponent varied between 0.6 and 2.0. The aerosol radiative forcing at the bottom of the atmosphere varied from –23 to –227,–34 to –199, and –29 to –191 W m^–2 for the whole haze period, while the aerosol radiative forcing at the top of the atmosphere varied from –4 to –98, –10 to –51, and –21 to –143 W m^–2 in Beijing, Shijiazhuang, and Jiaozuo, respectively. Satellite observations showed that smoke, polluted dust, and polluted continental components of aerosols may aggravate air pollution during haze episodes. The analysis of the potential source contribution function and concentration-weighted trajectory showed that the contribution from local emissions and pollutants transport from upstream areas were 190–450 and 100–410 μg m^–3, respectively.     

Estimation of the Aerosol Radiative Effect over the Tibetan Plateau Based on the Latest CALIPSO Product

Based on the CALIPSO (Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observation) Version 4.10 products released on 8 November 2016, the Level 2 (L2) aerosol product over the Tibetan Plateau (TP) is evaluated and the aerosol radiative effect is also estimated in this study. As there are still some missing aerosol data points in the daytime CALIPSO Version 4.10 L2 product, this study re-calculated the aerosol extinction coefficient to explore the aerosol radiative effect over the TP based on the CALIPSO Level 1 (L1) and CloudSat 2B-CLDCLASS-LIDAR products. The energy budget estimation obtained by using the AODs (aerosol optical depths) from calculated aerosol extinction coefficient as an input to a radiative transfer model shows better agreement with the Earth’s Radiant Energy System (CERES) and CloudSat 2B-FLXHR-LIDAR observations than that with the input of AODs from aerosol extinction coefficient from CALIPSO Version 4.10 L2 product. The radiative effect and heating rate of aerosols over the TP are further simulated by using the calculated aerosol extinction coefficient. The dust aerosols may heat the atmosphere by retaining the energy in the layer. The instantaneous heating rate can be as high as 5.5 K day^–1 depending on the density of the dust layers. Overall, the dust aerosols significantly affect the radiative energy budget and thermodynamic structure of the air over the TP, mainly by altering the shortwave radiation budget. The significant influence of dust aerosols over the TP on the radiation budget may have important implications for investigating the atmospheric circulation and future regional and global climate.     

北京等地对流层低层晴天气溶胶微物理特征

1982年4—7月对北京等地对流层低层晴天气溶胶数浓度、尺度谱分布进行了飞机观测。结果表明:来自西、西北和北部气团的气溶胶数浓度相当低（平均为10-1—100 /厘米3）。尺度谱分布用dn/dD=C/DA拟合，相关显著水平α≤0.01，幂指数A值多小于3（占总数73%以上），比Junge给出的A=4值小些。鉴于直径D=0.5—2微米粒子在大气中的重要性，也按dn/dD=C′/DB进行拟合，多数测值α≤0.01，少数α≤0.05。幂指数A、B和D=0.5—1微米粒子相对数浓度f1在水平、垂直方向上是相当均匀稳定的。受城市影响时，混合层内气溶胶数浓度明显增大，尺度谱分布斜率变陡（A、B增大），特别是和“气-粒”转化有关的D=1微米左右粒子数浓度增加非常显著，比不受城市影响时，增加了1—2个量级，最大可增加3个量级。可见，城市影响是造成混合层气溶胶数浓度增大、尺度谱分布变陡、局地大气污染加重、低层能见度变坏的重要原因。     

ATTILA: atmospheric tracer transport in a Lagrangian model

The model ATTILA has been developed to treat the global-scale transport of passive trace species in the atmosphere within the framework of a general circulation model (GCM). ATTILA runs online within the GCM ECHAM4 and advects the centroids of 80.000 to 190.000 constant mass air parcels. Each trace constituent is thereby represented by a mass mixing ratio in each parcel. ATTILA contains state-of-the-art parameterizations of convection, turbulent boundary layer mixing and inter-parcel transport, and provides an algorithm to map the tracer concentrations from the trajectories to the ECHAM model grid. The transport characteristics of ATTILA are evaluated against observations and the standard semi-Lagrangian transport scheme of ECHAM by two experiments. (1) We simulate the distribution of the short-lived tracer radon (²²²Rn) in order to examine fast vertical transport over continents, and long-range transport from the continents to remote areas. (2) We simulate the distribution of radiocarbon (¹⁴C) from nuclear weapon tests in order to examine upper tropospheric and stratospheric transport characteristics. Contrary to the semi-Lagrangian scheme, ATTILA shows a greatly reduced meridional transport in the upper troposphere and lower stratosphere, and a reduced downward flux from the stratosphere to the troposphere, especially in mid-latitudes. Since ATTILA is a numerically non-diffusive scheme, it is able to maintain steep gradients, which compare better to the observations than the rather smooth gradients produced by the semi-Lagrangian scheme.     

Investigation of the Planetary Boundary Layer in the Swiss Alps Using Remote Sensing and In Situ Measurements

The development of the planetary boundary layer (PBL) has been studied in a complex terrain using various remote sensing and in situ techniques. The high-altitude research station at Jungfraujoch (3,580 m a.s.l.) in the Swiss Alps lies for most of the time in the free troposphere except when it is influenced by the PBL reaching the station, especially during the summer season. A ceilometer and a wind profiler were installed at Kleine Scheidegg, a mountain pass close to Jungfraujoch, located at an altitude of 2,061 m a.s.l. Data from the ceilometer were analyzed using two different algorithms, while the signal-to-noise ratio of the wind profiler was studied to compare the retrieved PBL heights. The retrieved values from the ceilometer and wind profiler agreed well during daytime and cloud-free conditions. The results were additionally compared with the PBL height estimated by the numerical weather prediction model COSMO-2, which showed a clear underestimation of the PBL height for most of the cases but occasionally also a slight overestimation especially around noon, when the PBL showed its maximum extent. Air parcels were transported upwards by slope winds towards Jungfraujoch when the PBL was higher than 2,800 m a.s.l. during cloud-free cases. This was confirmed by the in situ aerosol measurements at Jungfraujoch with a significant increase in particle number concentration, particle light absorption and scattering coefficients when PBL-influenced air masses reached the station in the afternoon hours. The continuous aerosol in situ measurements at Jungfraujoch were clearly influenced by the local PBL development but also by long-range transport phenomena such as Saharan dust or pollution from the south.     

Aerosol Properties and Their Impacts on Surface CCN at the ARM Southern Great Plains Site during the 2011 Midlatitude Continental Convective Clouds Experiment

Aerosol particles are of particular importance because of their impacts on cloud development and precipitation processes over land and ocean. Aerosol properties as well as meteorological observations from the Department of Energy Atmospheric Radiation Measurement(ARM) platform situated in the Southern Great Plains(SGP) are utilized in this study to illustrate the dependence of continental cloud condensation nuclei(CCN) number concentration(NCCN) on aerosol type and transport pathways. ARM-SGP observations from the 2011 Midlatitude Continental Convective Clouds Experiment field campaign are presented in this study and compared with our previous work during the 2009–10 Clouds, Aerosol, and Precipitation in the Marine Boundary Layer field campaign over the current ARM Eastern North Atlantic site. Northerly winds over the SGP reflect clean, continental conditions with aerosol scattering coefficient(σ_(sp)) values less than 20 Mm~(-1) and NCCNvalues less than 100 cm~(-3). However, southerly winds over the SGP are responsible for the observed moderate to high correlation(R)among aerosol loading(σ_(sp) 60 Mm~(-1)) and NCCN, carbonaceous chemical species(biomass burning smoke), and precipitable water vapor. This suggests a common transport mechanism for smoke aerosols and moisture via the Gulf of Mexico,indicating a strong dependence on air mass type. NASA MERRA~(-2) reanalysis aerosol and chemical data are moderately to highly correlated with surface ARM-SGP data, suggesting that this facility can represent surface aerosol conditions in the SGP, especially during strong aerosol loading events that transport via the Gulf of Mexico. Future long-term investigations will help to understand the seasonal influences of air masses on aerosol, CCN, and cloud properties over land in comparison to over ocean.     

非洲地区大气气溶胶光学厚度时空变化及亚速尔高压对沙尘越大西洋传输的影响

研究了非洲地区大气气溶胶光学厚度（AOD）的时空变化及沙尘气溶胶越大西洋海区的传输。结果表明：1）源于撒哈拉沙漠的沙尘及其随赤道东风向西输送使得沙尘气溶胶成为非洲沙漠地区和紧邻的大西洋海区的主要气溶胶组分;AOD高值区和沙尘气溶胶光学厚度高值区在1—7月随赤道辐合带北移同步向北移动,而在8—12月则向南回撤。2）刚果盆地大气气溶胶主要为热带雨林和稀树草原排放的有机碳（OC）和黑碳（BC）气溶胶;其中与生物质燃烧源排放有关的OC、BC高值主要集中在干季（6—9月）的后半段（8—9月）;而生物源OC排放全年连续,其排放峰值出现于雨季开始时;生物质燃烧排放高值期与生物源排放高值期前后相继,形成干季（尤其是后半段）时期的OC、BC光学厚度高值。3）亚马逊河入海口地区主要气溶胶组分为海盐气溶胶,9—11月该区风力输送增强,风向由东南风转变为东风,海盐进入亚马逊河入海口处,形成AOD和海盐气溶胶光学厚度高值区。4）撒哈拉沙漠沙尘气溶胶向大西洋传输的偏北月份为7—9月、偏南月份为1—3月;2000—2016年海区沙尘气溶胶的传输路径存在向南移动的变化趋势,与同期亚速尔高压的增强和沙尘传输路径以北北风分量的增强以及赤道辐合带的移动一致。上述研究结果揭示了利用大气气溶胶时空变化特征反映区域大气环流和气候变化的可能性。     

我国北方地区对流层中下层臭氧收支

为了揭示我国北方地区对流层中下层臭氧(O₃) 的形成机理以及周边地区的污染输送对我国北方地区对流层中下层O₃收支的影响, 在与外场观测数据比较分析的基础上, 利用全球化学输送模式(MOZART-2) 采用收支分析方法定量分析了影响我国北方地区对流层中下层O₃的各个物理化学过程。结果表明:我国北方地区对流层下层O₃最重要的来源是光化学生成作用, 约占总来源的58.3%(41.5 Tg), 光化学生成反应中HO₂对于O₃生成的贡献最大; 最大的汇是干沉降过程, 约占总汇的43.2%(26.2Tg); 水平净输送作用对我国北方地区对流层中下层O₃收支的影响非常大, 在我国北方地区对流层下层, 41.6%左右的O₃来自水平净输送, 随高度增加, 水平输送影响增大, 我国北方地区对流层中层大约81.5%的O₃来自水平净输送。     

Atmospheric aerosol characterization in 2010 anomalous summer season in the Moscow region

Daily measurements of atmospheric aerosol characteristics were carried out in Dolgoprudny (Moscow region) in June–August 2010. The particle concentrations at 11 size gradations within the range of 0.01–10 μm and the concentrations of cloud condensation nuclei active at water vapor supersaturation of 0.2–1% were determined. It is shown that the long anticyclonic conditions and the burning of forests and peat bogs resulted in the increase in total aerosol concentration in surface air by more than 1.5 times and in concentrations of particles with the diameter of 0.1–1 μm and > 1 μm by 5 and 10 times, respectively. The fire smoke mainly consisted of the particles with the size of 0.1–3 μm. The particles with the size of more than 5 μm were not observed. The recurrent visibility decrease up to hundreds of meters was caused by the increase in the concentration of particles with the diameter of more than 0.32μm in the air. During the smoke blanketing, the concentration of active condensation nuclei in aerosol increased almost by 20 times that created an opportunity for watering of aerosol particles and formation of the acid smog.     

近10年东亚沙尘气溶胶时空分布与起尘通量的数值研究

利用一个耦合了沙尘模型的区域气候模式RegCM3和NCEP再分析资料,对近10年(2000-2009年)东亚地区沙尘气溶胶(直径≤20μm)时空分布特征和起尘通量进行了数值模拟。结果表明,(1)耦合模式能较好地模拟东亚地区沙尘气溶胶的时空分布特点。东亚地区沙尘气溶胶光学厚度、柱含量高值区主要位于塔克拉玛干沙漠和巴丹吉林沙漠。沙尘气溶胶柱含量的季节变化特征明显,春季最大,冬季次之,秋季最小。东亚地区110°E以东,沙尘主要以700hPa高度为中心向东传输。(2)东亚地区起沙源区主要位于塔克拉玛干沙漠、巴丹吉林沙漠、藏北沙漠化地区及蒙古国西南部,起沙强度存在明显的季节变化。2000-2009年东亚地区年平均起沙通量为1015.34mg.m-2.d-1,其中62.4%和2.3%分别通过干、湿过程重新沉降在东亚地区,其余35.3%被净释放进入大气或进行远距离传输。     

关于硝酸盐气溶胶光学特征和辐射强迫的研究进展

在过去的20多年里,中外对硫酸盐气溶胶做了大量的研究,对它在大气中的排放、含量、光学特征和辐射强迫有了深入的认识;由于硝酸盐气溶胶在大气中平均含量比硫酸盐低很多,因此过去人们对硝酸盐的研究没有给予重视。然而,近年来的研究表明,硝酸盐气溶胶的散射性质在某些波段甚至强于硫酸盐;同时,由于未来对人为硫酸盐前体物的减排,硫酸盐气溶胶排放会大幅度减少,而硝酸盐气溶胶的排放却增长迅速,其在人为气溶胶中所占的比重越来越高,将会导致其在未来造成的辐射强迫有可能超过硫酸盐,使得其在地区范围内和季节尺度上成为重要的辐射强迫和气候影响因子。中国是硝酸盐气溶胶排放量较大的地区,硝酸盐对未来中国气候和气候变化的影响显得越来越重要。因此,就近年来有关硝酸盐气溶胶的排放和在大气中的浓度变化、光学厚度分布特征及其辐射强迫的研究进展做了回顾和介绍,并对其未来的研究做了展望。