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1.
利用SBDART（Santa Barbara DISORT Atmospheric Radiative Transfer）辐射传输模式,结合AERONET（Aerosol Robotic Network）北京站观测的气溶胶光学特性数据,评估北京地区近十年气溶胶以及黑碳气溶胶的辐射强迫,主要研究结果如下:北京近十年气溶胶平均光学厚度（aerosol optical depth, AOD440nm）为0.61±0.56,?ngstr?m波长指数均值为1.09,单次散射反照率（single scattering albedo, SSA440nm）的均值为0.888±0.045;AOD呈现下降趋势,SSA呈上升趋势,表明该区域气溶胶污染有所改善。晴空条件下,大气层顶、地面和大气的气溶胶直接辐射强迫多年均值分别为?24.91±19.80 W m?2、?65.52±43.78 W m?2、40.61±28.62 W m?2,即气溶胶对大气层顶和地表为冷却效应,对大气产生加热作用。气溶胶和黑碳气溶胶的直接辐射强迫绝对值的年际变化表现为微弱的下降趋势,季节变化特征为春夏季高,冬季低,这与AOD的变化规律一致。并且黑碳气溶胶的直接辐射强迫下降趋势与SSA的上升趋势呈现较好的反位相关系。  相似文献   

2.
This study is based on ground-based measurements of downward surface shortwave irradiance (SW), columnar water vapour (wv), and aerosol optical depth (τ) obtained at Thule Air Base (Greenland) in 2007–2010, together with MODIS observations of the surface shortwave albedo (A). Radiative transfer model calculations are used in combination with measurements to separate the radiative effect of A (ΔSWA), wv (ΔSWwv), and aerosols (ΔSWτ) in modulating SW in cloud-free conditions. The shortwave radiation at the surface is mainly affected by water vapour absorption, which produces a reduction of SW as low as ?100 Wm?2 (?18%). The seasonal change of A produces an increase of SW by up to +25 Wm?2 (+4.5%). The annual mean radiative effect is estimated to be ?(21–22) Wm?2 for wv, and +(2–3) Wm?2 for A. An increase by +0.065 cm in the annual mean wv, to which corresponds an absolute increase in ΔSWwv by 0.93 Wm?2 (4.3%), has been observed to occur between 2007 and 2010. In the same period, the annual mean A has decreased by ?0.027, with a corresponding decrease in ΔSWA by 0.41 Wm?2 (?14.9%). Atmospheric aerosols produce a reduction of SW as low as ?32 Wm?2 (?6.7%). The instantaneous aerosol radiative forcing (RFτ) reaches values of ?28 Wm?2 and shows a strong dependency on surface albedo. The derived radiative forcing efficiency (FEτ) for solar zenith angles between 55° and 70° is estimated to be (?120.6 ± 4.3) for 0.1 < A < 0.2, and (?41.2 ± 1.6) Wm?2 for 0.5 < A < 0.6.  相似文献   

3.
对气溶胶气候效应开展分类评估并探讨诊断方法的合理性。人为气溶胶辐射效应对计算云辐射强迫的影响为0.38 W·m~(-2)。诊断评估气溶胶对云辐射强迫的影响需要排除这个偏差。两种基于不同试验设计诊断得出的半直接效应分别为0.21和0.09 W·m~(-2),存在显著差异。主要原因可能是人为气溶胶影响云辐射强迫的不同机制之间在模式模拟过程中不断地相互交织,不是简单的线性叠加关系。模式诊断得出的Twomey效应不仅包括Twomey效应本身,还包括Twomey效应引起的部分快速调整。总之,利用模式评估分析人为气溶胶气候效应需要注意审查试验设计和诊断方法的合理性。  相似文献   

4.
In this study, the annual and seasonal variations of all-sky and clear-sky surface solar radiation (SSR) in the eastern and central Tibetan Plateau (TP) during the period 1960–2009 are investigated, based on surface observational data, reanalyses and ensemble simulations with the global climate model ECHAM5-HAM. The mean annual all-sky SSR series shows a decreasing trend with a rate of ?1.00 Wm?2 decade?1, which is mainly seen in autumn and secondly in summer and winter. A stronger decrease of ?2.80 Wm?2 decade?1 is found in the mean annual clear-sky SSR series, especially during winter and autumn. Overall, these results confirm a tendency towards a decrease of SSR in the TP during the last five decades. The comparisons with reanalysis show that both NCEP/NCAR and ERA-40 reanalyses do not capture the decadal variations of the all-sky and clear-sky SSR. This is probably due to a missing consideration of aerosols in the reanalysis assimilation model. The SSR simulated with the ECHAM5-HAM global climate model under both all-sky and clear-sky conditions reproduce the decrease seen in the surface observations, especially after 1980. The steadily increasing aerosol optical depth (AOD) at 550 nm over the TP in the ECHAM5-HAM results suggests transient aerosol emissions as a plausible cause.  相似文献   

5.
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   

6.
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   

7.
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.  相似文献   

8.
人为气溶胶对中国东部冬季风影响的模拟研究   总被引：1，自引：1，他引：0       下载免费PDF全文
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。  相似文献   

9.
The present study deals with the aerosol optical properties which are assessed during the period 2007 to 2009 over Mohal (31.9oN, 77.12oE) in the northwestern Indian Himalaya, using ground-based measurements and multi-satellite data. The daily average value of aerosol optical depth (AOD) at 500?nm, ?ngstr?m exponent and turbidity coefficient are 0.24?±?0.08, 1.02?±?0.34 and 0.13?±?0.05, respectively. The comparative study of satellite and ground-based measurements reveals that the percentage retrieval for daily AOD at 550?nm over Mohal within the expected accuracy (???? p?? ?=?±0.05?±?0.15?? p?? ) is around 87%, with a significant correlation coefficient of 0.76. The present study suggests that the retrieval of AOD through satellite data is able to characterise the distribution of AOD over Mohal. However, further efforts are needed in order to eliminate systematic errors in the existing Moderate Resolution Imaging Spectroradiometer (MODIS) algorithm. The transport of desert dust and anthropogenic aerosol during high aerosol loading days caused a significant reduction in surface-reaching solar radiation by 149 and 117%, respectively. This large reduction in surface-reaching solar radiation increased the atmospheric heating rate by 0.93 and 0.72?K?day?1, respectively. This study indicates significant climatic implications due to the transport of aerosols in the northwestern Indian Himalaya.  相似文献   

10.
黄土高原半干旱区典型日吸收性气溶胶综合观测分析   总被引：2，自引：0，他引：2  
利用兰州大学半干旱气候与环境观测站的太阳光度计、激光雷达、微波辐射计综合观测资料,结合辐射传输模式分析了该地区秋季典型日2012年9月3~4日、21日和28日气溶胶物理特性、垂直分布特征,及其与气象条件的关系。研究时期的气溶胶主要为局地沙尘与人为污染混合气溶胶,吸收性明显,尺度较小。其中,4日西北风增强,远距离传输沙尘气溶胶,气溶胶光学厚度最大,粒子尺度明显增大。尝试利用灰色关联度法确定参考高度,分别为7.41 km、8.47 km、7.13 km和7.66 km,反演气溶胶消光系数,由此积分得到的光学厚度与太阳光度计观测值相关性可达0.975,反演效果较好。研究时期气溶胶的抬升主要受白天热力湍流作用,边界层发展,气溶胶向上传输,每日12时（当地时间,下同）至14时传输至最大高度,气溶胶抬升的高度对应大气加热率的高值区,低层加热率可达1 K d-1。气溶胶在大气层顶和地面造成负辐射强迫,分别为-12.707 W m-2、-25.398 W m-2,大气中表现为正辐射强迫,为12.692 W m-2,大气层顶的辐射强迫对气溶胶的物理特性最为敏感,当气溶胶吸收性明显时,大气层顶的瞬时辐射强迫会出现正值。  相似文献   

11.
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   

12.
Climate forcing by carbonaceous and sulfate aerosols   总被引：3，自引：0，他引：3  
 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  相似文献   

13.
The effect of anthropogenic emissions from China on global burdens of ozone, sulphate, organic carbon (OC) and black carbon (BC) aerosols is examined, using the three-dimensional chemistry transport model Oslo CTM2. Two model simulations were performed, the first with global present-day emissions and the second with the anthropogenic emissions from China set to their pre-industrial levels. The global radiative forcing for these species is then calculated. Industrial emissions from China are found to account for a 4–5% increase in the global burden of OC aerosol, the change in secondary organic aerosol being slightly less than that of primary organic aerosol. A 10% increase in the global sulphate aerosol burden is calculated, and the increase in BC is 23%. The global radiative forcing of aerosols from China was calculated to be −62, −3.7, −13 and 89 mW m−2, for sulphate, secondary organic, primary organic and BC aerosols, respectively. The increase in ozone causes a forcing of 77 mW m−2.  相似文献   

14.
In China, due to lack of countrywide monitoring and coarse emission inventory of black carbon (BC) in early years, there are large uncertainties as to the estimations of its loading, direct radiative forcing (DRF) and climate response. Here, we apply an up-to-date emission inventory of BC in 2006 to investigate its loading, optical depth (AOD) at 550?nm and DRF using the coupled Regional Climate Chemistry Modeling System (RegCCMS). A state of the art air quality model (WRF/Chem) is also used to access surface BC concentration. Simulated surface concentrations of BC from these two models were compared with observations, while the AOD was compared with the results both from the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model and from satellite and ground-based simulations. Results show that RegCCMS presented similar patterns and levels of annual mean-surface BC concentration to those of WRF/Chem. The regional distributions and monthly variations of RegCCMS BC were reproduced well in comparison to observations. Simulated pattern of AODs are consistent to but lower than those from satellite (Omi-0.25°) and AERONET simulations. Annual mean DRFs mainly distribute in the area with high BC loadings, with regional mean of 0.75?W?m?C2 and predicted global mean of 0.343?W?m?C2. In general, the results are about 0.4?C5 times for regional column burden, about 2 times as high for regional mean DRFs, about 1.3?C1.8 times for global mean DRFs and about 3?C4 times for AOD at 550?nm as compared to those in previous studies in China. These increasing DRFs of BC imply that its warming effect and climate response should be stronger and the DRF of total aerosols should be weaker (less negative).  相似文献   

15.
Industrial pollution has a significant effect on aerosol properties in Changsha City, a typical city of central China. Therefore, year-round measurements of aerosol optical, radiative and chemical properties from 2012 to 2014 at an urban site in Changsha were analyzed. During the observation period, the energy structure was continuously optimized, which was characterized by the reduction of coal combustion. The aerosol properties have obvious seasonal variations. The seasonal average aerosol optical depth (AOD) at 500 nm ranged from 0.49 to 1.00, single scattering albedo (SSA) ranged from 0.93 to 0.97, and aerosol radiative forcing at the top of the atmosphere (TOA) ranged from ?24.0 to 3.8 W m?2. The chemical components also showed seasonal variations. Meanwhile, the scattering aerosol, such as organic carbon, SO42?, NO3?, and NH4+ showed a decrease, and elemental carbon increased. Compared with observation in winter 2012, AOD and TOA decreased by 0.14 and ?1.49 W m?2 in winter 2014. The scattering components, SO42?, NO3? and NH4+, decreased by 12.8 μg m?3 (56.8%), 9.2 μg m?3 (48.8%) and 6.4 μg m?3 (45.2%), respectively. The atmospheric visibility and pollution diffusion conditions improved. The extinction and radiative forcing of aerosol were significantly controlled by the scattering aerosol. The results indicate that Changsha is an industrial city with strong scattering aerosol. The energy structure optimization had a marked effect on controlling pollution, especially in winter (strong scattering aerosol).  相似文献   

16.
The environmental impact of aerosols is currently a hot issue that has received worldwide attention. Lacking simultaneous observations of aerosols and carbon flux, the understanding of the aerosol radiative effect of urban agglomeration on the net ecosystem carbon exchange(NEE) is restricted. In 2009-2010, an observation of the aerosol optical property and CO_2 flux was carried out at the Dongguan Meteorological Bureau Station(DMBS) using a sun photometer and eddy covariance systems. The different components of photosynthetically active radiation(PAR),including global PAR(GPAR), direct PAR(DPAR), and scattered PAR(FPAR), were calculated using the Santa Barbara DISORT Atmospheric Radiative Transfer(SBDART) model. The effects of PAR on the NEE between land-atmosphere systems were investigated. The results demonstrated that during the study period the aerosol optical depth(AOD)reduced the DPAR by 519.28±232.89 μmol photons · m~(-2)s~(-1);, but increased the FPAR by 324.93±169.85μmol photons ·m~(-2)s~(-1);, ultimately leading to 194.34±92.62 μmol photons · m~(-2)s~(-1); decrease in the GPAR. All the PARs(including GPAR,DPAR, and FPAR) resulted in increases in the NEE(improved carbon absorption), but the FPAR has the strongest effect with the light use efficiency(LUE) being 1.12 times the values for the DPAR. The absorption of DPAR by the vegetation exhibited photo-inhibition in the radiation intensity 600 photons · m~(-2)s~(-1); in contrast, the absorptions of FPAR did not exhibit apparent photo-inhibition. Compared with the FPAR caused by aerosols, the DPAR was not the primary factor affecting the NEE. On the contrary, the increase in AOD significantly increased the FPAR, enhancing the LUE of vegetation ecosystems and finally promoting the photosynthetic CO_2 absorption.  相似文献   

17.
Black carbon concentration and weather data were online monitored continuously from March 2008 to February 2009 at the Akedala regional atmosphere station in the arid region of Central Asia. We present the daily, monthly and seasonal variations of BC concentration in the atmosphere and discuss the possible emission sources. Black carbon concentration in this region varies in the range of 43.7–1,559.2?ng/m3. A remarkable seasonal variation of BC in the aerosol was observed in the order of winter?>?spring?>?autumn?>?summer. The peak value of BC appeared at 10:00–13:00 while the lowest one at 7:00–9:00 each day. Air masses backward trajectories show the potential emission sources in the northwest from spring to autumn. Through back trajectory also revealed that BC in winter might be attributed to the emission from the anthropogenic activities, including domestic heating, cooking, combustion of oil and natural gas, and the medium-range transport from those cities in northern slope of Tianshan Mountains and Siberia. Some BC aerosols from the arid region of Central Asia were transported to the Pacific Ocean by the Westerlies.  相似文献   

18.

A Raman lidar system was operated along with the Microtops sunphotometer measurements to carry out the study of the variation of the optical properties of aerosols over Palampur (32.11° N and 76.53° E), India from 17th April to 11th May 2019. The lidar system is furnished with Raman (N2) channel and depolarization channel allowing independent measurement of Lidar Ratio (LR) and linear depolarization ratio. The study reveals that the majority of the aerosols approximately were restricted within the planetary boundary layer (PBL) and very less loading was present in the free troposphere over the study location. The particle loading over the study period was found to be very less with aerosol backscatter coefficient (at 355 nm) ranging from ～0.13 Mm?1sr?1 to ～7.25 Mm?1sr?1 with mean value of 2.67?±?0.82 Mm?1sr?1 and it is well supplemented by the mean aerosol optical depth (AOD) of 0.37?±?0.13 obtained from Microtops Sunphotometer. The average lidar ratio values for 0-1 km altitude (L1) 72?±?13sr, for 1-2 km (L2) altitude 55?±?8sr, for 2-3 km (L3) 54?±?15sr were observed as suggesting dominance of the biomass burning aerosols and anthropogenic aerosols. The particle depolarization ratio (355 nm) values were found from approximately 4.8?±?2.7% to 11.5?±?1.9% with the mean value of 7?±?1.3% suggesting the presence of non-spherical particles. To trace the sources of the pollution, we derived the HYSPLIT trajectory which shows the majority of the movement was from local sources.

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19.
The atmospheric aerosols can absorb moisture from the environment due to their hydrophilicity and thus affect atmospheric radiation fluxes. In this article, the ultraviolet radiation and relative humidity (RH) data from ground observations and a radiative transfer model were used to examine the influence of RH on ultraviolet radiation flux and aerosol direct radiative forcing under the clear-sky conditions. The results show that RH has a significant influence on ultraviolet radiation because of aerosol hygroscopicity. The relationship between attenuation rate and RH can be fitted logarithmically and all of the R2 of the 4 sets of samples are high, i.e. 0.87, 0.96, 0.9, and 0.9, respectively. When the RH is 60%, 70%, 80% and 90%, the mean aerosol direct radiative forcing in ultraviolet is ?4.22W m?2, ?4.5W m?2, ?4.82W m?2 and ?5.4W m?2, respectively. For the selected polluted air samples the growth factor for computing aerosol direct radiative forcing in the ultraviolet for the RH of 80% varies from 1.19 to 1.53, with an average of 1.31.  相似文献   

20.
西北地区气溶胶光学特性及辐射影响   总被引：3，自引：1，他引：2  
利用SACOL（兰州大学半干旱气候与环境观测站）2006~2012年AERONET（全球气溶胶自动监测网）level 2.0和太阳短波辐射计资料,分析了中国西北地区气溶胶的光学特性与辐射影响。利用辐射传输模式SBDART（平面平行大气辐射传输模式）检验TOA（大气层顶）处辐射强迫为正的原因。BOA（地表）、TOA、Atmosphere（大气）的辐射强迫年均值分别是-59.43 W m-2、-17.03 W m-2、42.40 W m-2,AOD（光学厚度,550 nm）年均值0.37,α（波段的波长指数,440~675 nm）年均值0.91,变化趋势与AOD位相相反,当AOD为0.3~2.2时,α很小（0.0~0.2）,表明粒子尺度很大。SSA（单次散射反照率,675 nm）年均值0.93,g（不对称因子,675 nm）年均值0.68,复折射指数（675 nm）实部年均值1.48,虚部0.007。复折射指数实部的年变化趋势与AOD一致,虚部与AOD反位相,所以西北地区多为粗模态散射性气溶胶。气溶胶对大气的加热率最大值出现在0~2 km,随高度递减。冬、夏半年在地表加热率分别是2.6 K d-1和0.6 K d-1;季节变化中,冬季、秋季、春季和夏季,在地表的加热率依次是2.5 K d-1、1.4 K d-1、1.2 K d-1和0.2 K d-1,主要因为秋季气溶胶的吸收性大于春季。地表反照率和SSA对TOA正辐射强迫贡献率分别是22.5%和77.5%。  相似文献   

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