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1.
庄炳亮  王体健  李树 《高原气象》2009,28(5):1095-1104
将区域气候模式(RegCM3)与对流层大气化学模式(TACM)耦合, 建立区域气候化学模拟系统(RegCCMS), 用以模拟研究中国地区黑碳气溶胶的空间分布、 第一间接辐射强迫及其气候效应。利用RegCCMS模式对2003年1月和7月进行模拟, 结果表明, 我国黑碳气溶胶主要集中在四川、 河北、 山东等地, 1月份浓度最高值中心在四川, 达到4 μg·m-3; 而在7月则出现在华中地区, 高值中心值为3.5 μg·m-3。地面浓度的季节差异不是很明显。1月和7月由黑碳气溶胶所造成的第一间接辐射强迫全国平均值分别为-0.389 W·m-2和-1.18 W·m-2, 局部地区达到-4~-4.5 W·m-2。敏感性试验结果表明, 考虑黑碳气溶胶的第一间接气候效应后, 使得近地面气温下降, 降水减少, 1月变化的平均值分别为-0.025K和-0.0027 mm·d-1, 7月变化的平均值分别为-0.16K和-0.095 mm·d-1, 在不同季节和地区, 气温和降水的变化存在明显差异。  相似文献   

2.
黑碳气溶胶辐射强迫全球分布的模拟研究   总被引:18,自引:3,他引:15  
张华  马井会  郑有飞 《大气科学》2008,32(5):1147-1158
利用一个改进的辐射传输模式,结合全球气溶胶数据集(GADS),计算晴空条件下冬夏两季黑碳气溶胶的直接辐射强迫在对流层顶和地面的全球分布。计算结果表明,与温室气体引起的整层大气都是正的辐射强迫不同,黑碳气溶胶的辐射强迫在对流层顶为正值,而在地面的辐射强迫却是负值。作者从理论上解释了造成这种结果的原因。对北半球冬季和夏季而言,在对流层顶黑碳气溶胶的全球辐射强迫的平均值分别为0.085W/m2和0.155 W/m2,在地面则分别为-0.37 W/m2和-0.63 W/m2。虽然气溶胶的辐射强迫主要依赖于其本身的光学性质和在大气中的浓度,太阳高度角和地表反照率对黑碳气溶胶的辐射强迫会产生很大的影响。研究指出:黑碳气溶胶在对流层顶正的辐射强迫和在地面负的辐射强迫的绝对值都随太阳天顶角的余弦和地表反照率的增加线性增大;地表反照率对黑碳气溶胶辐射强迫的强度和分布都有重要影响。黑碳气溶胶的辐射强迫分布具有明显的纬度变化特征,冬夏两季的大值区都位于30°N~90°N之间,表明人类活动是造成黑碳气溶胶辐射强迫的主要原因。  相似文献   

3.
黑碳气溶胶的辐射强迫及其对东亚的气候效应仍有较大不确定性,同时在黑碳气溶胶气候效应的研究中对海洋的关注较少。为了量化分析黑碳气溶胶直接辐射效应和分析其通过海气相互作用对东亚夏季风的影响,用区域海气耦合模式进行黑碳气溶胶离线模拟的敏感试验。试验结果表明:东亚晴空大气顶和地面的净辐射强迫在春季分别为1. 58 W·m~(-2)和~(-2). 75 W·m~(-2),在夏季分别为1. 68 W·m~(-2)和~(-2). 62 W·m~(-2)。受黑碳气溶胶辐射效应影响,大气变暖,大气热力稳定度增加,云量减少。春季黑碳气溶胶的"热泵效应"引起华南降水增加和夏季风提前爆发。夏季孟加拉湾海表降温,南支槽加深,引起华南降水增加;另外中纬度附近经向温度梯度增大,进而增强冷空气势力和水汽辐散,引起华北降水减少。华南降水正异常和华北降水负异常有利于"南涝北旱"。黑碳气溶胶辐射效应能通过海气相互作用增加热带海表温度,减小经向温度梯度和海陆热力差异,进而减弱夏季风。此外,黑碳气溶胶辐射效应也能增强局域哈德莱环流及北风,进而减弱夏季风。  相似文献   

4.
张天航  廖宏  常文渊  刘瑞金 《大气科学》2016,40(6):1242-1260
目前气候模式对沙尘气溶胶直接辐射强迫模拟仍有很大不确定性,多模式对比有助于定量评估不确定范围。国际大气化学—气候模式比较计划(Atmospheric Chemistry and Climate Model Intercomparison Project,ACCMIP)旨在评估当前模式对短寿命大气成分辐射强迫和气候效应的模拟能力。基于7个ACCMIP模式模拟的中国地区沙尘气溶胶浓度,我们评估了中国区域沙尘气溶胶直接辐射强迫和不确定性范围。结果显示,中国区域沙尘气溶胶年排放总量为215±163 Tg a-1,区域年均地表浓度为41±27 μg m-3,柱浓度为9±4 kg m-2,光学厚度为0.09±0.05。中国区域年均沙尘气溶胶产生的大气顶短波、长波和总辐射强迫分别为-1.3±0.8 W m-2、0.7±0.4 W m-2和-0.5±0.7 W m-2;地表短波、长波和总的辐射强迫值为-1.5±1.0 W m-2、1.8±0.9 W m-2和0.2±0.2 W m-2。沙尘气溶胶长波辐射强迫对沙尘浓度的垂直分布敏感。高层沙尘气溶胶浓度越大,其在大气顶产生更强的正值长波辐射强迫。然而,沙尘气溶胶短波辐射强迫主要受整层沙尘柱浓度控制,对沙尘浓度的垂直分布较不敏感。本文结果可为中国沙尘气溶胶的气候模拟提供参考。  相似文献   

5.
利用双向耦合的区域气候模式和大气化学模式系统, 研究了中国与邻近地区人为污染排放引起对流层臭氧变化和产生的辐射强迫.结果表明, 污染排放对对流层臭氧含量的影响有明显的季节变化, 对北方的影响不如南方显著, 西部的季节变化稳定且小于东部, 内陆污染地区各季节臭氧柱含量的变化量均较高.对整个模拟区域而言, 臭氧变化量的年平均值为30.928 DU, 春季最大为32.168 DU, 而空间分布变化在12~38 DU之间.臭氧变化量对北方地区辐射的影响较小, 而对低纬和华东地区影响较大, 臭氧变化量引起的晴空地气系统短波辐射强迫、长波辐射强迫的平均值分别是0.185 W·m-2和0.464 W·m-2, 标准化短波辐射强迫与净辐射强迫值为0.006 W·m-2·DU-1和0.021 W·m-2·DU-1.气候反馈过程对对流层臭氧含量的影响范围在-0.470~0.752 DU之间, 包含气候反馈过程的区域年平均臭氧变化量是30.942 DU.在气候反馈条件下, 臭氧变化量的短波和长波辐射强迫分别是0.249 W·m-2及 0.482 W·m-2, 标准化的短波与净辐射强迫值为0.008 W·m-2·DU-1和0.024 W·m-2·DU-1.臭氧变化量导致地表温度的变化范围在±0.80 K之间.  相似文献   

6.
利用耦合化学过程的区域气候模式RegCM3,模拟研究3种主要人为排放气溶胶(硫酸盐、黑碳、有机碳)对东亚区域气候的影响.计算分析近20 a来3种气溶胶的时空分布、综合辐射强迫作用及其对地面气温和降水的影响.模拟结果表明:3种气溶胶冬夏季分布有所不同,冬季气溶胶大值区主要分布在南方地区,而夏季大值区北移;气溶胶短波辐射强迫在大气层顶和地面均为负值;气溶胶的加入对东亚地区地表气温有明显影响,冬季降温中心位于四川盆地,夏季降温大值区位于华北地区.气溶胶直接气候效应使得冬季东亚大部分地区降水减少,夏季东亚地区降水与中国南方地区夏季气溶胶浓度有较好的相关关系,中国东部雨带有南移趋势.  相似文献   

7.
沙尘气溶胶辐射强迫全球分布的模拟研究   总被引:7,自引:2,他引:5  
张华  马井会  郑有飞 《气象学报》2009,67(4):510-521
为了定景了解沙尘气溶胶对气候的影响,文中利用一个改进的辐射传输模式,结合伞球气溶胶数据集(G-ADS),计算了晴空条件下,冬夏两季沙尘气溶胶的直接辐射强迫在对流层顶和地面的全球分布,并讨论了云对沙尘气溶胶辐射强迫的影响.计算结果表明,对北半球冬季和夏季而言,在对流层顶沙尘气溶胶的全球短波辐射强迫的平均值分别为-0.477和-0.501 W/m2;长波辐射强迫分别为0.11和0.085 W/m2;全球平均短波地面辐射强迫冬夏两季分别为-1.362和-1.559 W/m2;长波辐射强迫分别为0.274和0.23 W/m2.沙尘气溶胶在对流层顶和地面的负辐射强迫的绝对值郁随太阳天顶角的余弦和地表反照率的增加而增大;地表反照率对沙尘气溶胶辐射强迫的强度和分布都有重要影响.研究指出:云对沙尘气溶胶的直接辐射强迫的影响不仅取决于云量,而且取决于云的高度和云水路径,以及地面反照率和太阳高度角等综合因素.中云和低云对沙尘气溶胶在对流层顶的短波辐射强迫的影响比高云明显.云的存在都使对流层顶长波辐射强迫减少,其中低云的影响最为明显.因此,在估算沙尘气溶胶总的直接辐射强迫时,云的贡献不可忽视.  相似文献   

8.
气溶胶的气候效应近年来备受关注。区域气候模式能够在有限的计算资源下取得更高的分辨率,成为一种研究区域气候的有力工具。本文使用意大利国际理论物理中心(ICTP)开发的区域气候模式(Reg CM3),对2008年12月~2009年11月我国硫酸盐气溶胶的时空分布及其直接气候效应进行了模拟。研究表明受大气环流影响,硫酸盐气溶胶空间分布在夏季分布最广,而其最大平均季度柱浓度出现在四川盆地,达到了27mg·m-2。受特殊地形的影响,四川盆地上空在全年一直维持着高浓度的硫酸盐。硫酸盐气溶胶对直接辐射强迫与其柱浓度的分布有很好的相关性。直接辐射强迫在夏季分布最广,其数值达到了-2.99W·m-2,全年平均为-2.4W·m-2。硫酸盐的直接气候效应造成了地面气温下降,在夏季达到了-0.26℃,全年平均为-0.09℃。直接气候效应对降水总体表现为微弱的抑制作用,但不同区域,不同季节差异较大。  相似文献   

9.
中国地区大气气溶胶辐射强迫及区域气候效应的数值模拟   总被引:47,自引:5,他引:42  
利用太阳直接辐射日总量和日照时数等多年观测资料,反演了中国地区大气气溶胶0.75 μm光学厚度的年、月平均值,分析了我国大气气溶胶状况的时空分布特征。据此,在中国区域气候模式中考虑气溶胶的辐射影响,模拟中国地区气溶胶直接辐射强迫的大小及气候响应的季节变化特征。计算结果表明: 我国大气气溶胶光学厚度多年平均分布状况是以四川盆地为大值中心向四周减少;长江中下游武汉附近和南疆盆地为另两个大值中心;青藏高原为气溶胶低值区;我国绝大部分地区春季气溶胶光学厚度值最大,各地气溶胶光学厚度最小值出现的季节则有所不同。气溶胶辐射强迫介于-5.3~-13 W/m2之间;辐射强迫具有春、夏季大,秋、冬季小,冬季南方偏大,夏季北方偏大的特征。气溶胶辐射强迫的分布与其光学厚度的分布基本一致。由于气溶胶的影响,中国大陆地区地面气温均有所下降,四川盆地到长江中下游地区以及青藏高原北侧到河套地区降温最为明显,分别可达-0.4℃和-0.5℃。气候响应具有明显的季节特征。地面气温的变化除与辐射强迫的大小有关外,还受大气环流的影响。  相似文献   

10.
气候模式分辨率作为影响模式模拟结果的重要因素,其对气溶胶与云相互作用的影响尚未全面认识。利用公共大气模型CAM5.3在3种分辨率(2°、1°、0.5°)下,分别采用2000年和1850年气溶胶排放情景进行试验,检验提高分辨率是否能改进气候模式的模拟能力,分析不同分辨率下气溶胶气候效应的异同,探索模式分辨率对气溶胶气候效应数值模拟结果的影响。通过观测资料与模式结果对比发现,提高分辨率可以明显改进模式对总云量、云短波辐射强迫的模拟能力,0.5°分辨率下模拟结果与观测更接近,其他变量并无明显改善。在不同分辨率下,全球平均的气溶胶气候效应较为一致,总云量、云水路径均增加,云短波和长波辐射强迫均加强,而云顶的云滴有效半径和降水均减小,地面气温降低。不同分辨率下,气溶胶增加引起的气溶胶光学厚度、云水路径、地面温度、云短波和长波辐射强迫变化的纬向平均分布相似但大小存在差异;而降水和云量变化的纬向分布与大小均存在较大差异,在区域尺度上还存在较大的不确定性。全球平均而言, 0.5°分辨率下气溶胶的间接辐射强迫相比1°分辨率下的结果降低了2.5%,相比2°分辨率下的结果降低了6.4%。提高模式分辨率可以部分改进模式模拟能力,同时,气溶胶的间接效应随着模式分辨率的提高而减弱。但气溶胶引起的云量、降水的变化在不同分辨率下差异较大,存在较大的不确定性。   相似文献   

11.
The indirect radiative and climatic effects of sulfate and organic carbon aerosols over East Asia were investigated using a Regional Integrated Environment Model System (RIEMS) with an empirical aerosol-cloud parameterization.The first indirect radiative forcing was negative and ranged from-9-0 W m-2 in the domain.The maximum cooling,up to-9 W m-2,occurred in the Chongqing District in winter,whereas the cooling areas were larger during summer than in winter.Organic carbon (OC) aerosols were more abundant in winter than in summer,whereas the sulfate concentration during summer was much higher than during winter.The concentrations of sulfate and OC were comparable in winter,and sulfate played a dominant role in determining indirect radiative forcing in summer,whereas in winter,both sulfate and OC were important.The regional mean indirect radiative forcings were-0.73 W m-2 and-0.41 W m-2 in summer and winter,respectively.The surface cooling caused by indirect effects was more obvious in winter than that in summer.The ground temperature decreased by ~1.2 K in most areas of eastern China in winter,whereas in summer,the temperature decreased (~-1.5 K) in some regions,such as the Yangtze River region,but increased (~0.9 K) in the areas between the Yellow and Yangtze Rivers.In winter,the precipitation decreased by 0-6 mm in most areas of eastern China,but in summer,alternating bands of increasing (up to 80 mm) and decreasing (~-80 mm) precipitation appeared in eastern China.  相似文献   

12.
The regional climate model (RegCM3) and a tropospheric atmosphere chemistry model (TACM) were coupled, thus a regional climate chemistry modeling system (RegCCMS) was constructed, which was applied to investigate the spatial distribution of anthropogenic nitrate aerosols, indirect radiative forcing, as well as its climatic effect over China. TACM includes the thermodynamic equilibrium model ISORROPIA and a condensed gas-phase chemistry model. Investigations show that the concentration of nitrate aerosols is relatively high over North and East China with a maximum of 29 μg m-3 in January and 8 μg m-3 in July. Due to the influence of air temperature on thermodynamic equilibrium, wet scavenging of precipitation and the monsoon climate, there are obvious seasonal differences in nitrate concentrations. The average indirect radiative forcing at the tropopause due to nitrate aerosols is -1.63 W m-2 in January and -2.65 W m-2 in July, respectively. In some areas, indirect radiative forcing reaches $-$10 W m-2. Sensitivity tests show that nitrate aerosols make the surface air temperature drop and the precipitation reduce on the national level. The mean changes in surface air temperature and precipitation are -0.13 K and -0.01 mm d-1 in January and -0.09 K and -0.11 mm d-1 in July, respectively, showing significant differences in different regions.  相似文献   

13.
A coupled meteorology and aerosol/chemistry model WRF-Chem(Weather Research and Forecast model coupled with Chemistry) was used to conduct a pair of simulations with present-day(PD) and preindustrial(PI) emissions over East Asia to examine the aerosol indirect effect on clouds.As a result of an increase in aerosols in January,the cloud droplet number increased by 650 cm-3 over the ocean and East China,400 cm-3 over Central and Southwest China,and less than 200 cm-3 over North China.The cloud liquid water path(LWP) increased by 40-60 g m-2 over the ocean and Southeast China and 30 g m-2 over Central China;the LWP increased less than 5 g m-2 or decreased by 5 g m-2 over North China.The effective radius(Re) decreased by more than 4 μm over Southwest,Central,and Southeast China and 2μm over North China.In July,variations in cloud properties were more uniform;the cloud droplet number increased by approximately 250-400 cm-3,the LWP increased by approximately 30-50 g m-2,and Re decreased by approximately 3 ?m over most regions of China.In response to cloud property changes from PI to PD,shortwave(SW) cloud radiative forcing strengthened by 30 W m-2 over the ocean and 10 W m-2 over Southeast China,and it weakened slightly by approximately 2-10 W m-2 over Central and Southwest China in January.In July,SW cloud radiative forcing strengthened by 15 W m-2 over Southeast and North China and weakened by 10 W m-2 over Central China.The different responses of SW cloud radiative forcing in different regions was related to cloud feedbacks and natural variability.  相似文献   

14.
Previous observational studies have estimated anthropogenic aerosol direct radiative forcing over oceans without due consideration of cloudy-sky aerosols.However,when interaction between clouds and aerosols located below or above the cloud level is taken into account,the aerosol direct radiative forcing is larger by as much as 5 W m-2 in most mid-latitude regions in the Northern Hemisphere.  相似文献   

15.
Aerosol optical properties and direct radiative effects on surface irradiance were examined using seven years(2006–2012)of Cimel sunphotometer data collected at Panyu—the main atmospheric composition monitoring station in the Pearl River Delta(PRD) region of China. During the dry season(October to February), mean values of the aerosol optical depth(AOD)at 550 nm, the ?ngstr?m exponent, and the single scattering albedo at 440 nm(SSA) were 0.54, 1.33 and 0.87, respectively.About 90% of aerosols were dominated by fine-mode strongly absorbing particles. The size distribution was bimodal, with fine-mode particles dominating. The fine mode showed a peak at a radius of 0.12 μm in February and October(~0.10μm~3μm~(-2)). The mean diurnal shortwave direct radiative forcing at the surface, inside the atmosphere(FATM), and at the top of the atmosphere, was-33.4 ± 7.0, 26.1 ± 5.6 and-7.3 ± 2.7 W m~(-2), respectively. The corresponding mean values of aerosol direct shortwave radiative forcing per AOD were-60.0 ± 7.8, 47.3 ± 8.3 and-12.8 ± 3.1 W m~(-2), respectively. Moreover,during the study period, FATMshowed a significant decreasing trend(p 0.01) and SSA increased from 0.87 in 2006 to 0.91 in 2012, suggesting a decreasing trend of absorbing particles being released into the atmosphere. Optical properties and radiative impacts of the absorbing particles can be used to improve the accuracy of inversion algorithms for satellite-based aerosol retrievals in the PRD region and to better constrain the climate effect of aerosols in climate models.  相似文献   

16.
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.  相似文献   

17.
Modeling Study of Aerosol Indirect Effects on Global Climate with an AGCM   总被引:3,自引:0,他引:3  
Aerosol indirect effects (AIEs) on global climate were quantitatively investigated by introducing aerosol-cloud interaction parameterizations for water stratus clouds into an AGCM (BCC AGCM2.0.1), which was developed by the National Climate Center of the China Meteorological Administration. The study yielded a global annual mean of -1.14 W m-2 for the first indirect radiative forcing (IRF), with an obvious seasonal change. In summer, large forcing mainly occurred in mid to high latitudes of the Northern Hem...  相似文献   

18.
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   

19.
Why Is the Climate Forcing of Sulfate Aerosols So Uncertain?   总被引:2,自引:0,他引:2  
l. IntroductionAlthough the aerosol has been recognized as an important factor which has innuence onthe past, present and future climate for a long time, it still has much uncertainty in assessingits climate forcing. The direct radiative forcing of sulfate aerosols has been estimated rangingfrom --0.3 W/ m2 to --0.9 W/ m2 in recent publications (Charlson et al., l992, Kiehl andBriegleb l993; Taylor and Penner 1994, Boucher and Anderson l995, Kieh1 and Rodhe l995;Chuang et al., l997, Penne…  相似文献   

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