Direct Radiative Forcing and Climatic Effects of Aerosols over East Asia by RegCM3

The authors used a high-resolution regional climate model(RegCM3) coupled with a chemistry/aerosol module to simulate East Asian climate in 2006 and to test the climatic impacts of aerosols on regionalscale climate.The direct radiative forcing and climatic effects of aerosols(dust,sulfate,black carbon,and organic carbon) were discussed.The results indicated that aerosols generally produced negative radiative forcing at the top-of-the-atmosphere(TOA) over most areas of East Asia.The radiative forcing induced by aerosols exhibited significant seasonal and regional variations,with the strongest forcing occurring in summer.The aerosol feedbacks on surface air temperature and precipitation were clear.Surface cooling dominated features over the East Asian continental areas,which varied in the approximate range of-0.5 to-2°C with the maximum up to-3-C in summer over the deserts of West China.The aerosols induced complicated variations of precipitation.Except in summer,the rainfall generally varied in the range of-1 to 1 mm d-1 over most areas of China.     

Characteristics of Elemental Composition of PM2.5 in the Spring Period at Tongyu in the Semi-arid Region of Northeast China

Continuous observations of mass concentration and elemental composition of aerosol particles （PM2.5） were conducted at Tongyu, a semi-arid site in Northeast China in the spring of 2006. The average mass concentration of PM2.5 at Tongyu station was 260.9±274.4 μg m^-3 during the observation period. Nine dust events were monitored with a mean concentration of 528.0±302.7 μgm^-3. The PM2.5 level during non- dust storm （NDS） period was 111.65±63.37 μg m^-3. High mass concentration shows that fine-size particles pollution was very serious in the semi-arid area in Northeast China. The enrichment factor values for crust elements during the dust storm （DS） period are close to those in the NDS period, while the enrichment factor values for pollution elements during the NDS period are much higher than those in the DS period, showing these elements were from anthropogenic sources. The ratios of dust elements to Fe were relative constant during the DS period. The Ca/Fe ratio in dust aerosols at Tongyu is remarkably different from that observed in other source regions and downwind regions. Meteorological analysis shows that dust events at Tongyu are usually associated with dry, low pressure and high wind speed weather conditions. Air mass back-trajectory analysis identified three kinds of general pathways were associated with the aerosol particle transport to Tongyu, and the northwest direction pathway was the main transport route.     

Aerosol Type Identification Using PARASOL Multichannel Polarized Data

PARASOL （Polarization ＆ Anisotropy of Reflectances for Atmospheric Sciences coupled with Ob- servations from a Lidar） multi-channel and mul- ti-directional polarized data for different aerosol types were compared. The PARASOL polarized radiance data at 490 nm, 670 nm, and 865 nm increased with aerosol optical thickness （AOT） for fine-mode aerosols; however, the polarized radiances at 490 nm and 670 nm decreased as AOT increased for coarse dust aerosols. Thus, the vari- ation of the polarized radiance with AOT can be used to identify fine or coarse particle-dominated aerosols. Polar- ized radiances at three wavelengths for fine- and coarse-mode aerosols were analyzed and fitted by linear regression. The slope of the line for 670 nm and 490 nm wavelength pairs is less than 0.35 for dust aerosols. However, the value for fine-mode aerosols is greater than 0.60. The Support Vector Machine method （SVM） based on 12 vector features was used to discriminate clear sky, coarse dust aerosols, fine-mode aerosols, and cloud. Two cases were given and validated by AErosol RObotic NETwork （AERONET） measurements, MODIS （Mod- erate Resolution Imaging Spectroradiometer） FMF （Fine Mode Fraction at 550 nm） images, PARASOL RGB （Red Green Blue） images, and CALIOP （Cloud-Aerosol Lidar with Orthogonal Polarization） VFM （Vertical Feature Mask） data.     

春季中国东部气溶胶化学组成及其分布的模拟研究

本文利用区域空气质量模式RAQMS（Regional Air Quality Model System）,对2009年春季中国东部气溶胶主要化学成分及其分布进行了模拟研究。与泰山站观测资料的对比结果显示,模式能比较合理地反映气溶胶浓度的逐日变化特征。整体上,模式对无机盐气溶胶的模拟好,分别高估和低估黑碳和有机碳气溶胶浓度,其原因与排放源、二次有机气溶胶化学机制和模式分辨率的不确定性有关。模拟结果显示,春季气溶胶浓度高值主要集中于华北、四川东部、长江中下游等地区。受东南亚生物质燃烧和大气输送的影响,中国的云南和广西等地区有机碳浓度高于中国其他地区。中国西北部沙尘浓度较高,而且向东输送并影响到中国东部和南方部分地区。中国东部的华北、四川东部、长江中下游等地PM_2.5（空气动力学直径在2.5微米以下的颗粒物）污染严重,4月平均PM_2.5浓度超过了我国日平均PM_2.5浓度限值。中国东部泰山站的观测和模拟结果都显示近地面硝酸盐浓度超过硫酸盐,中国北部对流层中硝酸盐的柱含量也大于硫酸盐,而在中国南部则相反,这一方面与春季中国云量 南多北少的分布特征以及云内液相化学反应有关,另一方面也与南北温差对气溶胶形成的影响有关。就整个中国东部而言,虽然硫酸盐的柱含量（46 Gg）仍大于硝酸盐（42 Gg）,但比较接近,反映出我国氮氧化物排放迅速增加的趋势。春季中国地区对流层中PM₁₀（空气动力学直径在10微米以下的颗粒物）及其化学成分柱含量分别为:990.8 Gg（PM₁₀）,52.6 Gg（硫酸盐）,48.2 Gg（硝酸盐）,32.1 Gg（铵盐）,22.9 Gg（黑碳）和74.1 Gg（有机碳）,有机碳（OC）中一次有机碳（POC）和二次有机碳（SOC）分别占60%和40%,中国东部PM₁₀中人为气溶胶和沙尘分别占30%和70%,反映了春季沙尘对我国大气气溶胶的重要贡献。     

Geochemistry of regional background aerosols in the Western Mediterranean

The chemical composition of regional background aerosols, and the time variability and sources in the Western Mediterranean are interpreted in this study. To this end 2002–2007 PM speciation data from an European Supersite for Atmospheric Aerosol Research (Montseny, MSY, located 40 km NNE of Barcelona in NE Spain) were evaluated, with these data being considered representative of regional background aerosols in the Western Mediterranean Basin. The mean PM₁₀, PM_2.5 and PM₁ levels at MSY during 2002–2007 were 16, 14 and 11 µg/m³, respectively. After compiling data on regional background PM speciation from Europe to compare our data, it is evidenced that the Western Mediterranean aerosol is characterised by higher concentrations of crustal material but lower levels of OM + EC and ammonium nitrate than at central European sites. Relatively high PM_2.5 concentrations due to the transport of anthropogenic aerosols (mostly carbonaceous and sulphate) from populated coastal areas were recorded, especially during winter anticyclonic episodes and summer midday PM highs (the latter associated with the transport of the breeze and the expansion of the mixing layer). Source apportionment analyses indicated that the major contributors to PM_2.5 and PM₁₀ were secondary sulphate, secondary nitrate and crustal material, whereas the higher load of the anthropogenic component in PM_2.5 reflects the influence of regional (traffic and industrial) emissions. Levels of mineral, sulphate, sea spray and carbonaceous aerosols were higher in summer, whereas nitrate levels and Cl/Na were higher in winter. A considerably high OC/EC ratio (14 in summer, 10 in winter) was detected, which could be due to a combination of high biogenic emissions of secondary organic aerosol, SOA precursors, ozone levels and insolation, and intensive recirculation of aged air masses. Compared with more locally derived crustal geological dusts, African dust intrusions introduce relatively quartz-poor but clay mineral-rich silicate PM, with more kaolinitic clays from central North Africa in summer, and more smectitic clays from NW Africa in spring.     

Model analysis of influences of aerosol mixing state upon its optical properties in East Asia

The air quality model system RAMS (Regional Atmospheric Modeling System)-CMAQ (Models-3 Community Multi-scale Air Quality) coupled with an aerosol optical/radiative module was applied to investigate the impact of different aerosol mixing states (i.e., externally mixed, half externally and half internally mixed, and internally mixed) on radiative forcing in East Asia. The simulation results show that the aerosol optical depth (AOD) generally increased when the aerosol mixing state changed from externally mixed to internally mixed, while the single scattering albedo (SSA) decreased. Therefore, the scattering and absorption properties of aerosols can be significantly affected by the change of aerosol mixing states. Comparison of simulated and observed SSAs at five AERONET (Aerosol Robotic Network) sites suggests that SSA could be better estimated by considering aerosol particles to be internally mixed. Model analysis indicates that the impact of aerosol mixing state upon aerosol direct radiative forcing (DRF) is complex. Generally, the cooling effect of aerosols over East Asia are enhanced in the northern part of East Asia (Northern China, Korean peninsula, and the surrounding area of Japan) and are reduced in the southern part of East Asia (Sichuan Basin and Southeast China) by internal mixing process, and the variation range can reach 5 W m－2. The analysis shows that the internal mixing between inorganic salt and dust is likely the main reason that the cooling effect strengthens. Conversely, the internal mixture of anthropogenic aerosols, including sulfate, nitrate, ammonium, black carbon, and organic carbon, could obviously weaken the cooling effect.     

塔里木盆地沙尘气溶胶的柱质量密度特性

气溶胶质量密度是气溶胶重要的参数,它影响着大气中复杂的化学反应,也与气溶胶的传输过程和空间分布息息相关.基于MERRA-2再分析资料提供的气溶胶柱质量密度数据,研究了我国塔里木盆地1980—2018年长时间序列的沙尘气溶胶柱质量密度的时空分布特征.结果表明,沙尘气溶胶和沙尘PM_2.5气溶胶柱质量密度有很大的变化范围,平均值分别为0.33和0.086 g/m²,同时具有明显的年际、月和季节变化特征.沙尘气溶胶和沙尘PM_2.5气溶胶柱质量密度的年平均值在0.24~0.41和0.06~0.11 g/m²范围内变化;春季最大,其平均值分别为0.47和0.12 g/m²,冬季最小,其平均值分别为0.13和0.04 g/m²;月平均值最大出现在5月,分别为0.57和0.14 g/m²,最小在1月,分别为0.1和0.03 g/m².     

Comparative inverse analysis of satellite (MODIS) and ground (PM10) observations to estimate dust emissions in East Asia

Soil dust aerosol is the largest contributor to aerosol mass concentrations in the troposphere and has considerable effects on air quality and climate. Arid and semi-arid areas of East Asia are one of the important dust source regions thus it is crucial to understand dust mobilization and accurately estimate dust emissions in East Asia. However, present dust models still contain large uncertainties with dust emissions that remain a significant contributor to the overall uncertainties in the model. In this study, we attempt to reduce these uncertainties by using an inverse modeling technique and obtain optimized dust emissions. We use Moderate Resolution Imaging Spectrometer (MODIS) aerosol optical depths (AODs) and groundbased mass concentrations of particles less than 10 μm in aerodynamic diameter (PM₁₀) observations over East Asia in May 2007. The MODIS AODs are validated with AErosol RObotic NETwork (AERONET) AODs. The inversion uses the maximum a posteriori method and the GEOS-Chem chemical transport model (CTM) as a forward model. The model error is large over dust source regions including the Gobi Desert and Mongolia. We find that inverse modeling analyses from the MODIS and PM₁₀ observations consistently result in decrease of dust emissions over Mongolia and the Gobi Desert. Whereas over the Taklamakan Desert and Manchuria, the inverse modeling analyses from both observations yield contrast results such as increase of dust sources using MODIS AODs, while decrease of those using PM₁₀ observations. We discuss some limitations of both observations to obtain the optimized dust emissions and suggest several strategies for the improvement of dust emission estimates in the model.     

沙尘表面非均相吸附系数不确定性及其影响的数值模式研究

本文从实验气溶胶样品、实验技术和分析方法三个方面对以往的实验室研究结果进行综合分析, 归纳总结出适合东亚地区沙尘气溶胶的非均相吸附系数γ的参考值, 并利用区域大气化学模式, 模拟研究了非均相吸附系数γ的不确定性对东亚地区沙尘气溶胶非均相化学过程的影响。为了研究非均相反应对γ的敏感性, 针对其中四种物质(HNO3、N2O5、O3和SO2) 的γ上限值和下限值, 分别进行了T-up (上限值) 和T-low(下限值)两个敏感实验; 针对相对湿度对HNO3和N2O5非均相吸附系数的影响进行了T-rh敏感实验。模拟结果与观测资料进行了对比分析, 结果表明模式可以比较好地反映气态物质、气溶胶浓度的演变过程和非均相反应过程。考虑非均相反应后模拟的硫酸盐和硝酸盐浓度与观测值更接近一些。采用γ参考值的模拟结果总体上比采用γ上限值和γ下限值更合理, 把γ系数作为相对湿度的函数来处理比作为常数处理更合理。沙尘气溶胶通过非均相化学反应, 可以使模拟区域内SO2、NOx和O3的平均浓度下降, 使硫酸盐和硝酸盐颗粒物浓度增加, 采用γ参考值计算得到3 km以下的上述物质的变化率分别为－3.44%、－5.92%、－1.75%、5.22%和23.25%, 显示沙尘表面非均相化学反应对大气化学成分特别是气溶胶有较大的影响; 不同γ取值对上述物质变化率有一定影响, 其中对硝酸盐和臭氧的影响较大, T-up和T-low 模拟结果之间可以相差13.4%和10.1%。     

Source identification of PM2.5 particles measured in Gwangju, Korea

The UNMIX and Chemical Mass Balance (CMB) receptor models were used to investigate sources of PM_2.5 aerosols measured between March 2001 and February 2002 in Gwangju, Korea. Measurements of PM_2.5 particles were used for the analysis of carbonaceous species (organic (OC) and elemental carbon (EC)) using the thermal manganese dioxide oxidation (TMO) method, the investigation of seven ionic species using ion chromatography (IC), and the analysis of twenty-four metal species using Inductively Coupled Plasma (ICP)-Atomic Emission Spectrometry (AES)/ICP-Mass Spectrometry (MS). According to annual average PM_2.5 source apportionment results obtained from CMB calculations, diesel vehicle exhaust was the major contributor, accounting for 33.4% of the measured PM_2.5 mass (21.5 μg m^− 3), followed by secondary sulfate (14.6%), meat cooking (11.7%), secondary organic carbon (8.9%), secondary nitrate (7.6%), urban dust (5.5%), Asian dust (4.4%), biomass burning (2.8%), sea salt (2.7%), residual oil combustion (2.6%), gasoline vehicle exhaust (1.9%), automobile lead (0.5%), and components of unknown sources (3.4%). Seven PM_2.5 sources including diesel vehicles (29.6%), secondary sulfate (17.4%), biomass burning (14.7%), secondary nitrate (12.6%), gasoline vehicles (12.4%), secondary organic carbon (5.8%) and Asian dust (1.9%) were identified from the UNMIX analysis. The annual average source apportionment results from the two models are compared and the reasons for differences are qualitatively discussed for better understanding of PM_2.5 sources.Additionally, the impact of air mass pathways on the PM_2.5 mass was evaluated using air mass trajectories calculated with the Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) backward trajectory model. Source contributions to PM_2.5 collected during the four air mass patterns and two event periods were calculated with the CMB model and analyzed. Results of source apportionment revealed that the contribution of diesel traffic exhaust (47.0%) in stagnant conditions (S) was much higher than the average contribution of diesel vehicle exhaust (33.4%) during the sampling period. During Asian dust (AD) periods when the air mass passed over the Korean peninsula, Asian dust and secondary organic carbon accounted for 25.2 and 23.0% of the PM_2.5 mass, respectively, whereas Asian dust contributed only 10.8% to the PM_2.5 mass during the AD event when the air mass passed over the Yellow Sea. The contribution of biomass burning to the PM_2.5 mass during the biomass burning (BB) event equaled 63.8%.     

Modeling Study of the Impact of Heterogeneous Reactions on Dust Surfaces on Aerosol Optical Depth and Direct Radiative Forcing over East Asia in Springtime

The spatial distributions and interannual variations of aerosol concentrations,aerosol optical depth(AOD) ,aerosol direct radiative forcings,and their responses to heterogeneous reactions on dust surfaces over East Asia in March 2006-10 were investigated by utilizing a regional coupled climate-chemistry/aerosol model. Anthropogenic aerosol concentrations(inorganic+carbonaceous) were higher in March 2006 and 2008,whereas soil dust reached its highest levels in March 2006 and 2010,resulting in stronger aerosol radiative forcings in these periods.The domain and five-year(2006-10) monthly mean concentrations of anthropogenic and dust aerosols,AOD,and radiative forcings at the surface(SURF) and at the top of the atmosphere(TOA) in March were 2.4μg m-3,13.1μg m-3,0.18,-19.0 W m-2,and-7.4 W m-2,respectively.Heterogeneous reactions led to an increase of total inorganic aerosol concentration;however,the ambient inorganic aerosol concentration decreased,resulting in a smaller AOD and weaker aerosol radiative forcings.In March 2006 and 2010,the changes in ambient inorganic aerosols,AOD,and aerosol radiative forcings were more evident.In terms of the domain and five-year averages,the total inorganic aerosol concentrations increased by 13.7%(0.17μg m-3) due to heterogeneous reactions,but the ambient inorganic aerosol concentrations were reduced by 10.5%(0.13μg m-3) .As a result,the changes in AOD,SURF and TOA radiative forcings were estimated to be-3.9%(-0.007) ,-1.7%(0.34 W m-2) ,and-4.3%(0.34 W m-2) ,respectively,in March over East Asia.     

基于国际大气化学—气候模式比较计划模式数据评估未来气候变化对中国东部气溶胶浓度的影响

气候变化引起的地面气溶胶浓度变化与区域空气质量密切相关。本文利用“国际大气化学—气候模式比较计划”（Atmospheric Chemistry and Climate Model Intercomparison Project, ACCMIP）中4个模式的试验数据分析了RCP8.5情景下2000~2100年气候变化对中国气溶胶浓度的影响。结果显示,在人为气溶胶排放固定在2000年、仅考虑气候变化的影响时,2000~2100年气候变化导致中国北部地区（31°N~45°N, 105°E~122°E）硫酸盐、有机碳和黑碳气溶胶分别增加28%、21%和9%,硝酸盐气溶胶在中国东部地区减少30%。气候变化对细颗粒物（PM_2.5）浓度的影响有显著的季节变化特征,冬季PM_2.5浓度在中国东部减少15%,这主要是由硝酸盐气溶胶在冬季的显著减少造成的;夏季PM_2.5浓度在中国北部地区增加16%,而长江以南地区减少为9%,这可能与模式模拟的未来东亚夏季风环流的增强有关。     

The Seasonal Variations of Aerosols over East Asia as Jointly Inferred from MODIS and OMI

Data on aerosol optical thickness(AOT) and single scattering albedo(SSA) derived from Moderate Resolution Imaging Spectrometer(MODIS) and Ozone Monitoring Instrument(OMI) measurements,respectively,are used jointly to examine the seasonal variations of aerosols over East Asia.The seasonal signals of the total AOT are well defined and nearly similar over the land and over the ocean.These findings indicate a natural cycle of aerosols that originate primarily from natural emissions. In contrast,the small-sized aerosols represented by the fine-mode AOT,which are primarily generated over the land by human activities,do not have evident seasonalscale fluctuations.A persistent maximum of aerosol loadings centered over the Sichuan basin is associated with considerable amounts of fine-mode aerosols throughout the year.Most regions exhibit a general spring maximum. During the summer,however,the aerosol loadings are the most marked over north central China.This occurrence may result from anthropogenic fine particles,such as sulfate and nitrate.Four typical regions were selected to perform a covariation analysis of the monthly gridded AOT and SSA.Over southwestern and southeastern China,if the aerosol loadings are small to moderate they are composed primarily of the highly absorptive aerosols. However,more substantial aerosol loadings probably represent less-absorptive aerosols.The opposite covariation pattern occurring over the coastal-adjacent oceans suggests that the polluted oceanic atmosphere is closely correlated with the windward terrestrial aerosols.North central China is strongly affected by dust aerosols that show moderate absorption.This finding may explain the lower variability in the SSA that accompanies increasing aerosol loadings in this region.     

Assessment of Individual Direct Radiative Effects of Major Aerosol Species in East Asia

To assess individual direct radiative effects of diverse aerosol species on a regional scale,the air quality modeling system RAMS-CMAQ(Regional Atmospheric Modeling System and Community Multiscale Air Quality) coupled with an aerosol optical properties/radiative transfer module was used to simulate the temporal and spatial distributions of their optical and radiative properties over East Asia throughout 2005.Annual and seasonal averaged aerosol direct radiative forcing(ADRF) of all important aerosols and individual components,such as sulfate,nitrate,ammonium,black carbon(BC),organic carbon(OC),and dust at top-of-atmosphere(TOA) in clear sky are analyzed.Analysis of the model results shows that the annual average ADRF of all important aerosols was in the range of 0 to-18 W m?2,with the maximum values mainly distributed over the Sichuan Basin.The direct radiative effects of sulfate,nitrate,and ammonium make up most of the total ADRF in East Asia,being concentrated mainly over North and Southeast China.The model domain is also divided into seven regions based on different administrative regions or countries to investigate detailed information about regional ADRF variations over East Asia.The model results show that the ADRFs of sulfate,ammonium,BC,and OC were stronger in summer and weaker in winter over most regions of East Asia,except over Southeast Asia.The seasonal variation in the ADRF of nitrate exhibited the opposite trend.A strong ADRF of dust mainly appeared in spring over Northwest China and Mongolia.     

Mass concentration of PM10 and PM2.5 fine-dispersed aerosol fractions in the Eastern Gobi Desert

Results are presented of monitoring measurements of the mass concentration of PM₁₀ (particles with the size of less than 10 μm) and PM_2.5 (less than 2.5 μm) fine-dispersed aerosol fractions at the Sainshand and Zamyn-Üüd stations located in the Gobi Desert of Mongolia. Revealed are the annual variations of the mass concentration of PM₁₀ and PM_2.5 fine-dispersed aerosol fractions at these stations in 2008. The maximum values of monthly mean concentration during the year were observed in May in the period of dust storms. On the days with the steady calm weather, the mass concentrations of PM₁₀ and PM_2.5 varied within 5–8 μg/m³ (PM₁₀) and 3–5 μg/m³ (PM_2.5) at the Sainshand station. During the dust storms, the maximum values of concentration exceeded 1400 μg/m³ (PM₁₀) and 380 μg/m³ (PM_2.5) that is by 28 (PM₁₀) and 15 (PM_2.5) times higher than the maximum permissible concentration for the European Union. Results are given of studying the frequency and duration of dust storms in recent 20 years (1991–2010) in the Eastern Gobi Desert.     

Analysis and evaluation of the global aerosol optical properties simulated by an online aerosol-coupled non-hydrostatic icosahedral atmospheric model

Aerosol optical properties are simulated using the Spectral Radiation Transport Model for Aerosol Species(SPRINTARS)coupled with the Non-hydrostatic ICosahedral Atmospheric Model(NICAM). The 3-year global mean all-sky aerosol optical thickness(AOT) at 550 nm, the ngstr m Exponent(AE) based on AOTs at 440 and 870 nm, and the single scattering albedo(SSA) at 550 nm are estimated at 0.123, 0.657 and 0.944, respectively. For each aerosol species, the mean AOT is within the range of the Aero Com models. Both the modeled all-sky and clear-sky results are compared with observations from the Moderate Resolution Imaging Spectroradiometer(MODIS) and the Aerosol Robotic Network(AERONET). The simulated spatiotemporal distributions of all-sky AOTs can generally reproduce the MODIS retrievals, and the correlation and model skill can be slightly improved using the clear-sky results over most land regions. The differences between clear-sky and all-sky AOTs are larger over polluted regions. Compared with observations from AERONET, the modeled and observed all-sky AOTs and AEs are generally in reasonable agreement, whereas the SSA variation is not well captured. Although the spatiotemporal distributions of all-sky and clear-sky results are similar, the clear-sky results are generally better correlated with the observations. The clear-sky AOT and SSA are generally lower than the all-sky results, especially in those regions where the aerosol chemical composition is contributed to mostly by sulfate aerosol. The modeled clear-sky AE is larger than the all-sky AE over those regions dominated by hydrophilic aerosol, while the opposite is found over regions dominated by hydrophobic aerosol.     

近22 a人为气溶胶对东亚地区夏季风环流影响的数值模拟研究

运用区域气候模式RegCM3耦合入一个化学过程,对东亚地区三类人为排放气溶胶（硫酸盐、黑碳和有机碳）的时空分布特征及其对夏季风环流的影响进行了数值模拟研究。模拟结果显示,气溶胶的引入会引起东亚地区夏季850 hPa风场发生改变,我国江淮以东洋面上空出现了一个气旋式距平环流中心,中心以西的偏北风气流将削弱东亚地区夏季西南季风。通过讨论春季中国地区气溶胶浓度与夏季东亚地区850 hPa经向风的时滞关系,以及夏季中国地区气溶胶浓度与同期东亚地区850 hPa经向风的关系,可以发现,春、夏季中国地区气溶胶浓度均与夏季东亚地区850 hPa经向风有很好的负相关关系,当春季中国北方和夏季中国南方地区气溶胶浓度增加时,中国东部地区夏季偏南季风减弱。这可能与气溶胶改变了大气层顶和地表的辐射强迫,进而引起了海陆气压差异和位势高度场的变化有关。     

近22a人为气溶胶对东亚地区夏季风环流影响的数值模拟研究

运用区域气候模式RegCM3耦合入一个化学过程,对东亚地区三类人为排放气溶胶（硫酸盐、黑碳和有机碳）的时空分布特征及其对夏季风环流的影响进行了数值模拟研究.模拟结果显示,气溶胶的引入会引起东亚地区夏季850 hPa风场发生改变,我国江淮以东洋面上空出现了一个气旋式距平环流中心,中心以西的偏北风气流将削弱东亚地区夏季西南季风.通过讨论春季中国地区气溶胶浓度与夏季东亚地区850 hPa经向风的时滞关系,以及夏季中国地区气溶胶浓度与同期东亚地区850 hPa经向风的关系,可以发现,春、夏季中国地区气溶胶浓度均与夏季东亚地区850hPa经向风有很好的负相关关系,当春季中国北方和夏季中国南方地区气溶胶浓度增加时,中国东部地区夏季偏南季风减弱.这可能与气溶胶改变了大气层顶和地表的辐射强迫,进而引起了海陆气压差异和位势高度场的变化有关.     

东亚沙尘源区与下游地区气溶胶光学特性比较

利用AERONET观测资料从气候学的角度比较分析了2001-2011年东亚地区沙尘天气发生时沙尘源区和下游区大气气溶胶光学特性。结果表明：沙尘期间沙尘源区气溶胶光学厚度明显大于下游区,而Angstr?m波长指数却小于下游区,当沙尘暴出现时会降至零甚至负值。气溶胶粒子尺度体积谱分布除敦煌为单峰外,其余各站均呈双峰分布,香河和北京的细粒子浓度明显大于西北地区,这可能是由细的沙尘粒子和污染气溶胶共同造成。在440-1020 nm范围内,中国地区气溶胶单次散射反照率平均值为0.93,韩国和日本站分别为0.93和0.94。沙尘源区与下游区相比,复折射指数实部偏大,虚部偏小。总体来说,沙尘天气下东亚地区在4个波段内平均不对称因子为0.70。