A Review of Aerosol Optical Properties and Radiative Effects

Atmospheric aerosols influence the earth's radiative balance directly through scattering and absorbing solar radiation, and indirectly through affecting cloud properties. An understanding of aerosol optical properties is fundamental to studies of aerosol effects on climate. Although many such studies have been undertaken, large uncertainties in describing aerosol optical characteristics remain, especially regarding the absorption properties of different aerosols. Aerosol radiative effects are considered as either positive or negative perturbations to the radiation balance, and they include direct, indirect (albedo effect and cloud lifetime effect), and semi-direct effects. The total direct effect of anthropogenic aerosols is negative (cooling), although some components may contribute a positive effect (warming). Both the albedo effect and cloud lifetime effect cool the atmosphere by increasing cloud optical depth and cloud cover, respectively. Absorbing aerosols, such as carbonaceous aerosols and dust, exert a positive forcing at the top of atmosphere and a negative forcing at the surface, and they can directly warm the atmosphere. Internally mixed black carbon aerosols produce a stronger warming effect than externally mixed black carbon particles do. The semi-direct effect of absorbing aerosols could amplify this warming effect. Based on observational (ground-and satellite-based) and simulation studies, this paper reviews current progress in research regarding the optical properties and radiative effects of aerosols and also discusses several important issues to be addressed in future studies.     

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.     

气溶胶辐射效应在华东地区一次雾霾过程中的作用

利用WRF/Chem(Weather Research and Forecasting Model coupled with Chemistry)模拟了2013年12月华东地区一次雾、霾事件气溶胶辐射反馈效应对气象场和大气质量的影响。通过3个不同气溶胶浓度设置的试验区分气溶胶浓度不同辐射效应的影响。比较不同试验得出,本次雾、霾过程中,不论是气溶胶直接、半直接辐射效应还是间接效应均使污染地区短波辐射减少、2 m气温下降、大气边界层高度降低,不利于水汽与污染物的扩散,空气污染进一步加重,雾结构进一步稳定,并使雾的持续时间延长,发展高度更高;对于化学场来说,气溶胶直接、半直接辐射效应使污染地区PM_(2.5)浓度增大、消光系数增大、氮氧化物浓度增大,臭氧浓度降低;间接辐射效应使PM_(2.5)浓度和消光系数进一步增大,氮氧化物、臭氧浓度降低。综上所述,气溶胶辐射效应能使大气污染加重,并利于雾的发生、发展。     

A Modeling Study of the Effects of Direct Radiative Forcing Due to Carbonaceous Aerosol on the Climate in East Asia

The study investigated the effects of global direct radiative forcing due to carbonaceous aerosol on the climate in East Asia, using the CAM3 developed by NCAR. The results showed that carbonaceous aerosols cause negative forcing at the top of the atmosphere (TOA) and surface under clear sky conditions, but positive forcing at the TOA and weak negative forcing at the surface under all sky conditions. Hence, clouds could change the sign of the direct radiative forcing at the TOA, and weaken the forcing at the surface. Carbonaceous aerosols have distinct effects on the summer climate in East Asia. In southern China and India, it caused the surface temperature to increase, but the total cloud cover and precipitation to decrease. However, the opposite effects are caused for most of northern China and Bangladesh. Given the changes in temperature, vertical velocity, and surface streamflow caused by carbonaceous aerosol in this simulation, carbonaceous aerosol could also induce summer precipitation to decrease in southern China but increase in northern China.     

Impact of Anthropogenic Aerosols on Summer Precipitation in the Beijing–Tianjin–Hebei Urban Agglomeration in China:Regional Climate Modeling Using WRF-Chem

The WRF model with chemistry(WRF-Chem) was employed to simulate the impacts of anthropogenic aerosols on summer precipitation over the Beijing–Tianjin–Hebei urban agglomeration in China. With the aid of a high-resolution gridded inventory of anthropogenic emissions of trace gases and aerosols, we conducted relatively long-term regional simulations,considering direct, semi-direct and indirect effects of the aerosols. Comparing the results of sensitivity experiments with and without emissions, it was found that anthropogenic aerosols tended to enhance summer precipitation over the metropolitan areas. Domain-averaged rainfall was increased throughout the day, except for the time around noon. Aerosols shifted the precipitation probability distribution from light or moderate to extreme rain. Further analysis showed that the anthropogenic aerosol radiative forcing had a cooling effect at the land surface, but a warming effect in the atmosphere. However, enhanced convective strength and updrafts accompanied by water vapor increases and cyclone-like wind shear anomalies were found in the urban areas. These responses may originate from cloud microphysical effects of aerosols on convection, which were identified as the primary cause for the summer rainfall enhancement.     

Direct and semi-direct radiative effects of anthropogenic aerosols in the Western United States: Seasonal and geographical variations according to regional climate characteristics

The direct and semi-direct radiative effects of anthropogenic aerosols on the radiative transfer and cloud fields in the Western United States (WUS) according to seasonal aerosol optical depth (AOD) and regional climate are examined using a regional climate model (RCM) in conjunction with the aerosol fields from a GEOS-Chem chemical-transport model (CTM) simulation. The two radiative effects cannot be separated within the experimental design in this study, thus the combined direct- and semi-direct effects are called radiative effects hereafter. The CTM shows that the AOD associated with the anthropogenic aerosols is chiefly due to sulfates with minor contributions from black carbon (BC) and that the AOD of the anthropogenic aerosol varies according to local emissions and the seasonal low-level winds. The RCM-simulated anthropogenic aerosol radiative effects vary according to the characteristics of regional climate, in addition to the AOD. The effects on the top of the atmosphere (TOA) outgoing shortwave radiation (OSRT) range from ?0.2?Wm^?2 to ?1?Wm^?2. In Northwestern US (NWUS), the maximum and minimum impact of anthropogenic aerosols on OSRT occurs in summer and winter, respectively, following the seasonal AOD. In Arizona-New Mexico (AZNM), the effect of anthropogenic sulfates on OSRT shows a bimodal distribution with winter/summer minima and spring/fall maxima, while the effect of anthropogenic BC shows a single peak in summer. The anthropogenic aerosols affect surface insolation range from ?0.6?Wm^?2 to ?2.4?Wm^?2, with similar variations found for the effects on OSRT except that the radiative effects of anthropogenic BC over AZNM show a bimodal distribution with spring/fall maxima and summer/winter minima. The radiative effects of anthropogenic sulfates on TOA outgoing longwave radiation (OLR) and the surface downward longwave radiation (DLRS) are notable only in summer and are characterized by strong geographical contrasts; the summer OLR in NWUS (AZNM) is reduced (enhanced) by 0.52?Wm^?2 (1.14?Wm^?2). The anthropogenic sulfates enhance (reduce) summer DLRS by 0.2?Wm^?2 (0.65?Wm^?2) in NWUS (AZNM). The anthropogenic BC affect DLRS noticeably only in AZNM during summer. The anthropogenic aerosols affect the cloud water path (CWP) and the radiative transfer noticeably only in summer when convective clouds are dominant. Primarily shortwave-reflecting anthropogenic sulfates decrease and increase CWP in AZNM and NWUS, respectively, however, the shortwave-absorbing anthropogenic BC reduces CWP in both regions. Due to strong feedback via convective clouds, the radiative effects of anthropogenic aerosols on the summer radiation field are more closely correlated with the changes in CWP than the AOD. The radiative effect of the total anthropogenic aerosols is dominated by the anthropogenic sulfates that contribute more than 80% of the total AOD associated with the anthropogenic aerosols.     

Dependence of climate forcing and response on the altitude of black carbon aerosols

Black carbon aerosols absorb solar radiation and decrease planetary albedo, and thus can contribute to climate warming. In this paper, the dependence of equilibrium climate response on the altitude of black carbon is explored using an atmospheric general circulation model coupled to a mixed layer ocean model. The simulations model aerosol direct and semi-direct effects, but not indirect effects. Aerosol concentrations are prescribed and not interactive. It is shown that climate response of black carbon is highly dependent on the altitude of the aerosol. As the altitude of black carbon increases, surface temperatures decrease; black carbon near the surface causes surface warming, whereas black carbon near the tropopause and in the stratosphere causes surface cooling. This cooling occurs despite increasing planetary absorption of sunlight (i.e. decreasing planetary albedo). We find that the trend in surface air temperature response versus the altitude of black carbon is consistent with our calculations of radiative forcing after the troposphere, stratosphere, and land surface have undergone rapid adjustment, calculated as “regressed” radiative forcing. The variation in climate response from black carbon at different altitudes occurs largely from different fast climate responses; temperature dependent feedbacks are not statistically distinguishable. Impacts of black carbon at various altitudes on the hydrological cycle are also discussed; black carbon in the lowest atmospheric layer increases precipitation despite reductions in solar radiation reaching the surface, whereas black carbon at higher altitudes decreases precipitation.     

Elicitation of Expert Judgments of Aerosol Forcing

A group of twenty-four leading atmospheric and climate scientists provided subjective probability distributions that represent their current judgment about the value of planetary average direct and indirect radiative forcing from anthropogenic aerosols at the top of the atmosphere. Separate estimates were obtained for the direct aerosol effect, the semi-direct aerosol effect, cloud brightness (first aerosol indirect effect), and cloud lifetime/distribution (second aerosol indirect effect). Estimates were also obtained for total planetary average forcing at the top of the atmosphere and for surface forcing. Consensus was strongest among the experts in their assessments of the direct aerosol effect and the cloud brightness indirect effect. Forcing from the semi-direct effect was thought to be small (absolute values of all but one of the experts' best estimates were ≤0.5 W/m²). There was not agreement about the sign of the best estimate of the semi-direct effect, and the uncertainty ranges some experts gave for this effect did not overlap those given by others. All best estimates of total aerosol forcing were negative, with values ranging between −0.25 W/m² and −2.1 W/m². The range of uncertainty that a number of experts associated with their estimates, especially those for total aerosol forcing and for surface forcing, was often much larger than that suggested in 2001 by the IPCC Working Group 1 summary figure (IPCC, 2001).     

A modeling study of the effects of aerosols on clouds and precipitation over East Asia

The National Center for Atmospheric Research Community Atmosphere Model (version 3.5) coupled with the Morrison?CGettelman two-moment cloud microphysics scheme is employed to simulate the aerosol effects on clouds and precipitation in two numerical experiments, one representing present-day conditions (year?2000) and the other the pre-industrial conditions (year?1750) over East Asia by considering both direct and indirect aerosol effects. To isolate the aerosol effects, we used the same set of boundary conditions and only altered the aerosol emissions in both experiments. The simulated results show that the cloud microphysical properties are markedly affected by the increase in aerosols, especially for the column cloud droplet number concentration (DNC), liquid water path (LWP), and the cloud droplet effective radius (DER). With increased aerosols, DNC and LWP have been increased by 137% and 28%, respectively, while DER is reduced by 20%. Precipitation rates in East Asia and East China are reduced by 5.8% and 13%, respectively, by both the aerosol??s second indirect effect and the radiative forcing that enhanced atmospheric stability associated with the aerosol direct and first indirect effects. The significant reduction in summer precipitation in East Asia is also consistent with the weakening of the East Asian summer monsoon, resulting from the decreasing thermodynamic contrast between the Asian landmass and the surrounding oceans induced by the aerosol??s radiative effects. The increase in aerosols reduces the surface net shortwave radiative flux over the East Asia landmass, which leads to the reduction of the land surface temperature. With minimal changes in the sea surface temperature, hence, the weakening of the East Asian summer monsoon further enhances the reduction of summer precipitation over East Asia.     

不同污染条件下气溶胶对短波辐射通量影响的模拟研究

将高光谱分辨率的气溶胶光学参数化方案应用于高精度的辐射传输模式BCC_RAD（974带）中,研究不同污染状况下气溶胶在地表与近地层大气中造成的直接辐射强迫与辐射强迫效率。发现气溶胶在地表产生的直接辐射强迫为负,在近地层大气中产生的直接辐射强迫为正,且随气溶胶浓度的升高变大,说明大气气溶胶的含量越高,单位气溶胶光学厚度产生的直接辐射强迫越大。将短波划分为3个波段:紫外、可见光和近红外,发现在紫外、可见光和近红外波段中,不同污染状况下气溶胶在地表造成的直接辐射强迫范围分别为:-1.36—-13.66、-3.03—-32.41和-2.74—-28.62 W/m2,在近地层大气中产生的直接辐射强迫范围分别为0.44—4.26、0.99—9.80和0.93—8.87 W/m2。通过进一步对比自然和人为气溶胶的影响,发现人为气溶胶在地表和大气层顶产生的负直接辐射强迫以及对整层和近地面大气造成的正直接辐射强迫均大于自然气溶胶的影响,且上述两种排放源的气溶胶对整层大气辐射收支的影响主要集中在800 hPa高度以下的大气中。按照地表直接辐射强迫大小来分析不同种类气溶胶的影响,结果为硫酸盐>有机碳>黑碳>海盐>沙尘;按照近地层大气直接辐射强迫大小排序则为黑碳>有机碳>沙尘>海盐>硫酸盐。最后,通过分析散射型气溶胶与吸收型气溶胶对辐射通量的影响,还探究了大气中散射与吸收过程的异同。      

Aerosol Microphysical and Radiative Effects on Continental Cloud Ensembles

Aerosol–cloud–radiation interactions represent one of the largest uncertainties in the current climate assessment. Much of the complexity arises from the non-monotonic responses of clouds, precipitation and radiative fluxes to aerosol perturbations under various meteorological conditions. In this study, an aerosol-aware WRF model is used to investigate the microphysical and radiative effects of aerosols in three weather systems during the March 2000 Cloud Intensive Observational Period campaign at the US Southern Great Plains. Three simulated cloud ensembles include a low-pressure deep convective cloud system, a collection of less-precipitating stratus and shallow cumulus, and a cold frontal passage. The WRF simulations are evaluated by several ground-based measurements. The microphysical properties of cloud hydrometeors, such as their mass and number concentrations, generally show monotonic trends as a function of cloud condensation nuclei concentrations.Aerosol radiative effects do not influence the trends of cloud microphysics, except for the stratus and shallow cumulus cases where aerosol semi-direct effects are identified. The precipitation changes by aerosols vary with the cloud types and their evolving stages, with a prominent aerosol invigoration effect and associated enhanced precipitation from the convective sources. The simulated aerosol direct effect suppresses precipitation in all three cases but does not overturn the aerosol indirect effect. Cloud fraction exhibits much smaller sensitivity(typically less than 2%) to aerosol perturbations, and the responses vary with aerosol concentrations and cloud regimes. The surface shortwave radiation shows a monotonic decrease by increasing aerosols, while the magnitude of the decrease depends on the cloud type.     

Direct Climatic Effect of Aerosols and Interdecadal Variations over East Asia Investigated by a Regional Coupled Climate-chemistry/aerosol Model

The direct climatic effect of aerosols for the 1980-2000 period over East Asia was numerically investigated by a regional scale coupled climate-chemistry/aerosol model,which includes major anthropogenic aerosols(sulfate,black carbon,and organic carbon) and natural aerosols(soil dust and sea salt) .Anthropogenic emissions used in model simulation are from a global emission inventory prepared for the Intergovernmental Panel on Climate Change Fifth Assessment Report(IPCC AR5) ,whereas natural aerosols are calculated online in the model.The simulated 20-year average direct solar radiative effect due to aerosols at the surface was estimated to be in a range of-9--33 W m-2 over most areas of China,with maxima over the Gobi desert of West China,and-12 W m-2 to-24 W m-2 over the Sichuan Basin,the middle and lower reaches of the Yellow River and the Yangtze River.Aerosols caused surface cooling in most areas of East Asia,with maxima of-0.8-C to-1.6-C over the deserts of West China,the Sichuan Basin,portions of central China,and the middle reaches of the Yangtze River. Aerosols induced a precipitation decrease over almost the entire East China,with maxima of-90 mm/year to-150 mm/year over the Sichuan Basin,the middle reaches of the Yangtze River and the lower reaches of the Yellow River.Interdecadal variation of the climate response to the aerosol direct radiative effect is evident,indicating larger decrease in surface air temperature and stronger perturbation to precipitation in the 1990s than that in the 1980s,which could be due to the interdecadal variation of anthropogenic emissions.     

人为气溶胶对中国东部冬季风影响的模拟研究

采用美国国家大气研究中心(NCAR)的公共大气模式CAM5.1研究了人为气溶胶排放增加对中国东部冬季风的影响,同时通过对比中国东部地区不同人为气溶胶排放源的敏感性试验结果,探讨了人为硫酸盐、黑碳及总人为气溶胶(硫酸盐+黑碳)增加对东亚冬季风的影响。结果表明:冬季硫酸盐气溶胶排放增加的直接和第一间接效应减少了到达地表的短波辐射通量,引起了陆地地表和对流层低层降温,海平面气压升高,增加了海陆间气压梯度,使得东亚冬季风增强。其第二间接效应导致中国南部大尺度降水率减少;黑碳气溶胶排放增加导致到达地表的短波辐射通量减少和大气中短波辐射通量增加,其半直接效应部分抵消了直接效应,故地表温度变化微小且不显著。加热的对流层低层导致中国南部对流活动和对流降水率增加;总人为气溶胶排放增加导致的大气温度变化表现为弱的降温作用,引起中国北部对流和大尺度降水率减少,而南部对流降水率增加。总人为气溶胶和黑碳气溶胶排放增加是导致中国北(南)部的东亚冬季风增强(减弱)的重要因素。     

A numerical simulation of aerosols’ direct effects on tropopause height

The direct effects of sulfate aerosol, dust aerosol, carbonaceous aerosol, and total combined aerosols on the tropopause height are simulated with the Community Atmospheric Model version 3.1 (CAM3.1). A decrease of global mean tropopause height induced by sulfate, carbonaceous aerosol, and total combined aerosols is found, and a tropopause height increase is induced by dust aerosol. Sulfate aerosol decreases the tropospheric temperature and increases the stratospheric temperature. These effects cause a decrease in the height of the tropopause. In contrast, carbonaceous and total combined aerosols increase both the tropospheric and the stratospheric temperatures, and they also cause a decrease in the height of the tropopause. The changes in the tropopause height show highly statistically significant correlations with the changes in the tropospheric and stratospheric temperatures. The changes in the tropospheric and stratospheric temperatures are related to the changes in the radiative heat rate, cloud cover, and latent heat, but none of these factors absolutely dominate the temperature change.     

Climate forcing by carbonaceous and sulfate aerosols

 An atmospheric general circulation model is coupled to an atmospheric chemistry model to calculate the radiative forcing by anthropogenic sulfate and carbonaceous aerosols. The latter aerosols result from biomass burning as well as fossil fuel burning. The black carbon associated with carbonaceous aerosols is absorbant and can decrease the amount of reflected radiation at the top-of-the-atmosphere. In contrast, sulfate aerosols are reflectant and the amount of reflected radiation depends nonlinearly on the relative humidity. We examine the importance of treating the range of optical properties associated with sulfate aerosol at high relative humidities and find that the direct forcing by anthropogenic sulfate aerosols can decrease from −0.81 W m^-2 to −0.55 Wm^-2 if grid box average relative humidity is not allowed to increase above 90%. The climate forcing associated with fossil fuel emissions of carbonaceous aerosols is calculated to range from +0.16 to +0.20 Wm^-2, depending on how much organic carbon is associated with the black carbon from fossil fuel burning. The direct forcing of carbonaceous aerosols associated with biomass burning is calculated to range from −0.23 to −0.16 Wm^-2. The pattern of forcing by carbonaceous aerosols depends on both the surface albedo and the presence of clouds. Multiple scattering associated with clouds and high surface albedos can change the forcing from negative to positive. Received: 29 September 1997 / Accepted: 10 June 1998     

Influence of aerosol-radiative forcings on the diurnal and seasonal cycles of rainfall over West Africa and Eastern Atlantic Ocean using GCM simulations

Effects of aerosol radiative forcing on the diurnal and seasonal cycles of precipitation over West Africa and eastern Atlantic Ocean are investigated for the boreal summer season: June–July–August. An eight year (2000–2007) average of GCM simulated rainfall data is compared with the corresponding TRMM rainfall data. The comparison shows that the amplitude of the diurnal cycles of rainfall over land and ocean are reasonably well simulated. Over land, the phase of the simulated diurnal cycle of precipitation peaks several hours earlier than that of the TRMM data. Corresponding differences over the ocean(s) are relatively smaller. Some of the key features of the aerosol induced model simulated field anomalies are: (a) aerosol direct radiative forcing which increases the atmospheric stability and reduces the daytime moist convection and convective precipitation; (b) the aerosol induced changes in the diurnal cycle of precipitation are out of phase with those of the TRMM data over land, but are in-phase over the ocean; (c) aerosols reduce the amplitude of the diurnal cycle of precipitation over land and enhance it over ocean. However, the phase of the diurnal cycle is not affected much by the aerosol radiative forcing both over land and ocean. During the boreal summer, aerosol radiative forcing and induced circulation and precipitation cool the Sahel and the southern part of Sahara desert more than the adjacent areas to the north and south, thereby shifting the peak meridional temperature gradient northward. Consequently, an anomalous easterly jet is found north of its climatological location. This anomalous jet is associated with increased cyclonic circulation to the south of its axis, resulting in an anomalous monsoon rain belt in the Sahel.     

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.     

Direct Radiative Forcing of Anthropogenic Aerosols over Oceans from Satellite Observations

Anthropogenic aerosols play an important role in the atmospheric energy balance. Anthropogenic aerosol optical depth (AOD) and its accompanying shortwave radiative forcing (RF) are usually simulated by nu- merical models. Recently, with the development of space-borne instruments and sophisticated retrieval algorithms, it has become possible to estimate aerosol radiative forcing based on satellite observations. In this study, we have estimated shortwave direct radiative forcing due to anthropogenic aerosols over oceans in all-sky conditions by combining clouds and the Single Scanner Footprint data of the Clouds and Earth’s Radiant Energy System (CERES/SSF) experiment, which provide measurements of upward shortwave fluxes at the top of atmosphere, with Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol and cloud products. We found that globally averaged aerosol radiative forcing over oceans in the clear-sky conditions and all-sky conditions were -1.03±0.48 W m-2 and -0.34 ±0.16 W m-2, respectively. Direct radiative forcing by anthropogenic aerosols shows large regional and seasonal variations. In some regions and in particular seasons, the magnitude of direct forcing by anthropogenic aerosols can be comparable to the forcing of greenhouse gases. However, it shows that aerosols caused the cooling effect, rather than warming effect from global scale, which is different from greenhouse gases.     

青藏高原地区气溶胶直接辐射强迫的数值模拟研究

通过比较EMAC模式模拟结果和卫星观测结果证实了模式的可信性,进而利用模拟结果分析研究了2010～2012年青藏高原上空气溶胶光学厚度及其直接辐射强迫的时空分布规律。结果表明:所有气溶胶组分中,沙尘、水溶性气溶胶和气溶胶中液态水是高原的主要消光物质,三者年平均消光占比分别为0.27、0.20和0.49。2011年夏季纳布罗火山爆发,高空气溶胶消光在海拔14 km以上显著增强。青藏高原气溶胶在大气顶和地表的直接辐射强迫分布总体上由北向南递减,沙尘气溶胶在高原北部边缘大气顶产生正辐射强迫,气溶胶大气层直接辐射强迫对大气有增温效应,主要出现在沙尘含量高的地区。此外,受纳布罗火山爆发的影响,平流层气溶胶在2011年秋、冬季产生了明显较强的负辐射强迫,相比于无火山爆发的2010年和 2012年,青藏高原上空平流层气溶胶负辐射强迫在2011年秋季和冬季分别增加了55.50%和52.38%。     

Impact of Different Aerosols on the Evolution of the Atmospheric Boundary Layer

The present work analyzes the effect of aerosols on the evolution of the atmospheric boundary layer (ABL) over Shangdianzi in Beijing.A one-dimensional ABL model and a radiative transfer scheme are incorporated to develop the structure of the ABL.The diurnal variation of the atmospheric radiative budget,atmospheric heating rate,sensible and latent heat fluxes,surface and the 2 m air temperatures as well as the ABL height,and its perturbations due to the aerosols with different single-scattering albedo (SSA) are studied by comparing the aerosol-laden atmosphere to the clean atmosphere.The results show that the absorbing aerosols cause less reduction in surface evaporation relative to that by scatting aerosols,and both surface temperature and 2 m temperature decrease from the clean atmosphere to the aerosol-laden atmosphere.The greater the aerosol absorption,the more stable the surface layer.After 12:00 am,the 2 m temperature increases for strong absorption aerosols.In the meantime,there is a slight decrease in the 2 m temperature for purely scattering aerosols due to radiative cooling.The purely scattering aerosols decrease the ABL temperature and enhance the capping inversion,further reducing the ABL height.