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1.
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.  相似文献   

2.
高玮  屈文军 《山东气象》2018,38(4):81-92
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。  相似文献   

3.
利用2004~2009年秋季臭氧监测仪的3级观测资料,分析了华北及周边地区的气溶胶光学性质。结果表明:大部分区域气溶胶光学厚度(Aerosol Optical Depth,AOD)和气溶胶紫外吸收指数(Ultra Violet Aerosol Index,UVAI)平均值分别高于0.8和0.75;高气溶胶事件发生频次统计表明,AOD高值(>0.4)频发于北京及其周边地区,UVAI高值(>1.0)频发于河北中部及南部地区;华北及其周边地区绝大多数城市平均AOD和UVAI分别高于0.7和0.60,而张家口、承德和阳泉3个城市的平均AOD和UVAI值分别低于0.6和0.65。作者进一步研究了2006年10月30日的一次霾事件中气溶胶的光学性质以及其时空分布特征。结果表明,霾由华北地区输送至渤海海域,并向东北方向输送;香河地基EZlidar激光雷达的垂直观测结果进一步表明,工业和城市型气溶胶主要集中在1500m以下,其中高浓度部分集中于650m以下,平均峰值位于285m,平均消光系数达2.15km-1;CALIOP卫星观测资料结合后向轨迹分析表明,大气低层气溶胶类型以工业和城市型气溶胶为主,而高层则由于上游大气输送沙尘粒子的混入使气溶胶类型转变为污染—沙尘型。霾事件期间,香河站CE-318太阳光度计观测的AOD平均值(标准差)从背景值0.08(0.04)升高至1.17(0.14);ngstrm指数平均值(标准差)从背景值0.90(0.10)升至1.12(0.09);核模态、积聚模态和粗模态的气溶胶粒子数柱总量均增加,其中细粒子所占比例明显升高。  相似文献   

4.
Aerosol observational data for 2012 obtained from Dunhuang Station of CARE-China(Campaign on Atmospheric Aerosol Research Network of China) were analyzed to achieve in-depth knowledge of aerosol optical properties over Dunhuang region. The results showed that the annual average aerosol optical depth(AOD) at 500 nm was 0.32 ± 0.06, and the ?ngstr?m exponent(α) was 0.73 ± 0.27. Aerosol optical properties revealed significant seasonal characteristics. Frequent sandstorms in MAM(March–April–May) resulted in the seasonal maximum AOD, 0.41 ± 0.04, and a relatively smaller αvalue, 0.44 ± 0.04. The tourism seasons, JJA(June–July–August) and SON(September–October–November) coincide with serious emissions of small anthropogenic aerosols. While in DJF(December–January–February), the composition of the atmosphere was a mixture of dust particles and polluted aerosols released by domestic heating; the average AOD and αwere 0.29 ± 0.02 and 0.66 ± 0.17, respectively. Different air masses exhibited different degrees of influence on the aerosol concentration over Dunhuang in different seasons. During MAM, ranges of AOD(0.11–1.18) and α(0.06–0.82) were the largest under the dust influence of northwest-short-distance air mass in the four trajectories. Urban aerosols transported by northwest-short-distance air mass accounted for a very large proportion in JJA and the mixed aerosols observed in SON were mainly conveyed by air masses from the west. In DJF, the similar ranges of AOD and α under the three air mass demonstrated the analogous diffusion effects on regional pollutants over Dunhuang.  相似文献   

5.
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。  相似文献   

6.
Characterization of aerosols is required to reduce uncertainties in satellite retrievals of global aerosols and for modeling the effects of these aerosols on climate.Aerosols in the North China Plain(NCP) are complex,which provides a good opportunity to study key aerosol optical properties for various aerosol types.A cluster analysis of key optical properties obtained from Aerosol Robotic Network(AERONET) data in Beijing and Xianghe during 2001-11 was performed to identify dominant aerosol types and their associated optical properties.Five dominant aerosol types were identified.The results show that the urban/industrial aerosol of moderate absorption was dominant in the region and that this type varied little with season.Urban/industrial aerosol of weak absorption was the next most common type and mainly occurs in summer,followed by that strong aerosols occurring mainly in winter.All were predominantly fine mode particles.Mineral dust(MD) and polluted dust(PD) occurred mainly in spring,followed by winter,and their absorption decreased with wavelength.In addition,aerosol dynamics and optical parameters such as refractive index and asymmetry factor were examined.Results show that the size of coarse mode particles decreased with AOD indicating the domination of external mixing between aerosols.  相似文献   

7.
Assuming spheroidal and spherical particle shapes for mineral dust aerosols, the effect of particle shape on dust aerosol optical depth retrievals, and subsequently on instantaneous shortwave direct radiative forcing (SWDRF) at the top of the atmosphere (TOA), is assessed based on Moderate Resolution Imaging Spectroradiometer (MODIS) data for a case study. Specifically, a simplified aerosol retrieval algorithm based on the principle of the Deep Blue aerosol retrieval method is employed to retrieve dust aerosol optical depths, and the Fu-Liou radiative transfer model is used to derive the instantaneous SWDRF of dust at the TOA for cloud-free conditions. Without considering the effect of particle shape on dust aerosol optical depth retrievals, the effect of particle shape on the scattering properties of dust aerosols (e.g., extinction efficiency, single scattering albedo and asymmetry factor) is negligible, which can lead to a relative difference of at most 5% for the SWDRF at the TOA. However, the effect of particle shape on the SWDRF cannot be neglected provided that the effect of particle shape on dust aerosol optical depth retrievals is also taken into account for SWDRF calculations. The corresponding results in an instantaneous case study show that the relative differences of the SWDRF at the TOA between spheroids and spheres depend critically on the scattering angles at which dust aerosol optical depths are retrieved, and can be up to 40% for low dust-loading conditions.  相似文献   

8.
Aerosol optical depth(AOD) is the most basic parameter that describes the optical properties of atmospheric aerosols,and it can be used to indicate aerosol content. In this study, we assimilated AOD data from the Fengyun-3 A(FY-3 A) and MODIS meteorological satellite using the Gridpoint Statistical Interpolation three-dimensional variational data assimilation system. Experiments were conducted for a dust storm over East Asia in April 2011. Each 0600 UTC analysis initialized a24-h Weather Research and Forecasting with Chemistry model forecast. The results generally showed that the assimilation of satellite AOD observational data can significantly improve model aerosol mass prediction skills. The AOD distribution of the analysis field was closer to the observations of the satellite after assimilation of satellite AOD data. In addition, the analysis resulting from the experiment assimilating both FY-3 A/MERSI(Medium-resolution Spectral Imager) AOD data and MODIS AOD data had closer agreement with the ground-based values than the individual assimilation of the two datasets for the dust storm over East Asia. These results suggest that the Chinese FY-3 A satellite aerosol products can be effectively applied to numerical models and dust weather analysis.  相似文献   

9.
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.  相似文献   

10.
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.  相似文献   

11.
Taking winter and summer in eastern China as an example application, a grid-cell method of aerosol direct radiative forcing(ADRF) calculation is examined using the Santa Barbara DISORT Atmospheric Radiative Transfer(SBDART) model with inputs from MODIS and AERONET observations and reanalysis data. Results show that there are significant seasonal and regional differences in climatological mean aerosol optical parameters and ADRF. Higher aerosol optical depth(AOD)occurs in summer and two prominent high aerosol loading centers are observed. Higher single scattering albedo(SSA) in summer is likely associated with the weak absorbing secondary aerosols. SSA is higher in North China during summer but higher in South China during winter. Aerosols induce negative forcing at the top of the atmosphere(TOA) and surface during both winter and summer, which may be responsible for the decrease in temperature and the increase in relative humidity.Values of ADRF at the surface are four times stronger than those at the TOA. Both AOD and ADRF present strong interannual variations; however, their amplitudes are larger in summer. Moreover, patterns and trends of ADRF do not always correspond well to those of AOD. Differences in the spatial distributions of ADRF between strong and weak monsoon years are captured effectively. Generally, the present results justify that to calculate grid-cell ADRF at a large scale using the SBDART model with observational aerosol optical properties and reanalysis data is an effective approach.  相似文献   

12.
基于新耦合气溶胶气候模式FGOALS-f3-L模拟分析了2002-2011年青藏高原地区气溶胶时空分布特征.结果表明:青藏高原地区,沙尘,硫酸盐,碳质气溶胶(包括黑碳,有机碳和混合碳)地表质量浓度分别占比为53.6%,32.2%,14.2%;在拉萨站点,模拟的气溶胶地表质量浓度被低估,尤其是黑碳和有机碳气溶胶;模拟的气溶胶光学厚度(AOD)时空分布与卫星观测结果较为一致,均方根误差和偏差分别为0.081和0.036;由于模式中沙尘排放参数化的不确定性,模式对AOD的模拟效果在夏季和秋季优于春季.  相似文献   

13.
This study presents the simulated aerosol spatiotemporal characteristics over the Tibetan Plateau (TP) with a newly developed coupled aerosol–climate model (FGOALS-f3-L). The aerosol properties are simulated over the TP for the period 2002–11. The results indicate that soil dust, sulfate, and carbonaceous aerosols (black carbon (BC), organic carbon (OC) and BC/OC) account for 53.6%, 32.2%, and 14.2% of the total aerosol mass over the TP, respectively. The simulated aerosol surface mass concentrations and aerosol optical depths (AODs) are evaluated with ground-based and satellite observations, respectively. Underestimations of the aerosol surface mass concentration are found at the Lhasa site, especially for BC and OC. The spatial distribution and interannual variation of AOD are consistent with MODIS observations, with the RMSE of 0.081 and bias of 0.036. Due to the uncertainty of the parameterization of dust emissions, the model's performance in summer and autumn is much better than that in spring.摘要基于新耦合气溶胶气候模式FGOALS-f3-L模拟分析了2002–2011年青藏高原地区气溶胶时空分布特征.结果表明:青藏高原地区, 沙尘,硫酸盐,碳质气溶胶 (包括黑碳,有机碳和混合碳) 地表质量浓度分别占比为53.6%, 32.2%, 14.2%;在拉萨站点, 模拟的气溶胶地表质量浓度被低估, 尤其是黑碳和有机碳气溶胶;模拟的气溶胶光学厚度 (AOD) 时空分布与卫星观测结果较为一致, 均方根误差和偏差分别为0.081和0.036;由于模式中沙尘排放参数化的不确定性, 模式对AOD的模拟效果在夏季和秋季优于春季  相似文献   

14.
A comparative study on the vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai was conducted based on the data obtained from a micro pulse lidar.There was a distinct difference in layer thickness and extinction coefficient under the two types of weather conditions.Aerosols were concentrated below 1 km and the aerosol extinction coefficients ranged from 0.25 to 1.50km-1 on haze days.In contrast,aerosols with smaller extinction coefficients(0.20 0.35 km-1) accumulated mainly from the surface to 2 km on floating dust days.The seasonal variations of extinction and aerosol optical depth(AOD) for both haze and floating dust cases were similar greatest in winter,smaller in spring,and smallest in autumn.More than 85%of the aerosols appeared in the atmosphere below 1 km during severe haze and floating dust weather.The diurnal variation of the extinction coefficient of haze exhibited a bimodal shape with two peaks in the morning or at noon,and at nightfall,respectively.The aerosol extinction coefficient gradually increased throughout the day during floating dust weather.Case studies showed that haze aerosols were generated from the surface and then lifted up,but floating dust aerosols were transported vertically from higher altitude to the surface.The AOD during floating dust weather was higher than that during haze.The boundary layer was more stable during haze than during floating dust weather.  相似文献   

15.
利用2006年3~5月天空辐射计观测数据反演得到北京地区春季大气气溶胶光学性质参数,包括大气气溶胶光学厚度(0.5μm)、Angstrm指数、单次散射反射比和粒子谱分布特征。结果表明:北京地区春季气溶胶平均光学厚度0.67,Angstrm指数0.54,单次散射比0.88,粒子吸收性质较弱,粒子谱呈双峰形,以粗粒子为主,粗、细模态粒子粒径分别集中在0.17μm和7.7μm左右。相比2004年此次观测期间气溶胶粒径较大,粒子体积浓度较高,散射作用在其消光特性中的比重略有下降。光学厚度日变化呈单峰型,日间单次散射比随时间逐渐递减,Angstrm指数在上午递减趋势明显,午后变得稳定。对同时观测的天空辐射计与CE-318不同波长光学厚度结果进行比较,结果显示两者得到的光学厚度相关性很好,各波长小时平均结果的相对误差小于7%。  相似文献   

16.
In this study, a regional air quality model system (RAQMS) was applied to investigate the spatial distributions and seasonal variations of atmospheric aerosols in 2006 over East Asia. Model validations demonstrated that RAQMS was able to reproduce the evolution processes of aerosol components reasonably well. Ground-level PM10 (particles with aerodynamic diameter ≤10 μm) concentrations were highest in spring and lowest in summer and were characterized by three maximum centers: the Taklimakan Desert (~1000 μg m-3), the Gobi Desert (~400 μg m-3), and the Huabei Plain (~300 μm-3) of China. Vertically, high PM10 concentrations ranging from 100 μg m-3 to 250 μg m-3 occurred from the surface to an altitude of 6000 m at 30o--45oN in spring. In winter, the vertical gradient was so large that most aerosols were restricted in the boundary layer. Both sulfate and ammonium reached their highest concentrations in autumn, while nitrate reached its maximum level in winter. Black carbon and organic carbon aerosol concentrations reached maximums in winter. Soil dust were strongest in spring, whereas sea salt exerted the strongest influence on the coastal regions of eastern China in summer. The estimated burden of anthropogenic aerosols was largest in winter (1621 Gg) and smallest in summer (1040 Gg). The sulfate burden accounted for ~42% of the total anthropogenic aerosol burden. The dust burden was about twice the anthropogenic aerosol burden, implying the potentially important impacts of the natural aerosols on air quality and climate over East Asia.  相似文献   

17.
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.  相似文献   

18.
不同污染条件下气溶胶对短波辐射通量影响的模拟研究   总被引:1,自引:0,他引:1  
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。   相似文献   

19.
使用RegCM3-dust区域气候模式,单向嵌套MIROC3.2-hires全球模式输出结果,在IPCCA1B温室气体排放情景下,对中国及东亚地区进行了当代(1991年-2000年)和未来(2091年-2100年)水平分辨率为50km的气候以及沙尘气溶胶数值模拟试验。结果表明,模式对中国地区地面气温、降水和东亚沙尘气溶胶空间分布模拟较好。未来东亚沙尘气溶胶年平均起沙通量增加2%,其中12月-3月由于地表积雪量的减少而增加,4月-11月由于10m风速的减小而减少,不同强度的强起沙事件同样12月-3月增加,4月-11月减少。年平均沙尘气溶胶柱含量增加14%,其中3月-5月和8月略减少,其它月份增加。沙尘气溶胶引起地面(SRF)负辐射强迫和沙尘源区大气顶(TOA)正辐射强迫、下游地区TOA负辐射强迫,受沙尘气溶胶辐射强迫的影响,地面起沙通量和柱含量减少。  相似文献   

20.
It is well established that aerosols affect the climate in a variety of ways. In order to understand these effects, we require an insight into the properties of aerosols. In this paper we present a study of aerosol properties such as aerosol optical depth (AOD), single scattering albedo (SSA) and aerosol radiative forcing (ARF) over mega city of Lahore (Pakistan). The data from Aerosol Robotic Network (AERONET) have been used for the period December 2009 to October 2011. The seasonal average values of AOD, asymmetry parameter (ASY) and volume size distribution in coarse mode were observed to be highest in summer. On the other hand, the average values of Angstrom exponent (AE) and imaginary part of refractive index (RI) were found to be maximum in winter. The average value of real part of RI was found to be higher in spring than in all other seasons. The SSA exhibited an increasing trend with wavelength in the range 440 nm–1020 nm in spring, summer and fall indicating the dominance of coarse particles (usually dust). However, a decreasing trend was found in winter in the range 675 nm–1020 nm pointing towards the dominance of biomass and urban/industrial aerosols. As far as aerosol radiative forcing (ARF) is concerned, we have found that during the spring season ARF was lowest at the surface of Earth and highest at top of the atmosphere (TOA). This indicates that the atmosphere was warmer in spring than in all the remaining seasons.  相似文献   

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