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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.
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   

3.
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   

4.
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   

5.
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   

6.
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   

7.
利用Terra和Aqua卫星上的MODIS探测反演气溶胶产品,比较分析了中国中东部和印度次大陆地区的气溶胶物理特性的异同。研究结果表明:中国中东部气溶胶类型以烟尘为主,印度次大陆地区东、西部分别以烟尘和沙尘为主。两地气溶胶光学厚度均有明显的年际变化,冬季低,夏季高。在夏季,两地烟尘所占比例都很大,且光学厚度也大,故两地污染状况都比较严重。总体来说,中国中东部地区污染程度要高于印度次大陆地区。  相似文献   

8.
In order to understand the seasonal variation of aerosol optical properties in the Yangtze River Delta,5 years of measurements were conducted during September 2005 to December 2009 at Taihu,China.The monthly averages of aerosol optical depth were commonly >0.6;the maximum seasonal average(0.93) occurred in summer.The magnitude of the Angstr¨om exponent was found to be high throughout the year;the highest values occurred in autumn(1.33) and were the lowest in spring(1.08).The fine modes of volume size distribution showed the maxima(peaks) at a radius of ~0.15 μm in spring,autumn,and winter;at a radius of ~0.22 μm in summer.The coarse modes showed the maxima(peaks) at a radius of 2.9 μm in spring,summer,and autumn and at a radius of 3.8 μm in winter.The averages of single-scattering albedo were 0.92(spring),0.92(summer),0.91(autumn),and 0.88(winter).The averages of asymmetry factor were found to be larger in summer than during other seasons;they were taken as 0.66 at 440-1020 nm over Taihu.The real part of the refractive index showed a weak seasonal variation,with averages of 1.48(spring),1.43(summer),1.45(autumn),and 1.48(winter).The imaginary parts of the refractive index were higher in winter(0.013) than in spring(0.0076),summer(0.0092),and autumn(0.0091),indicating that the atmosphere in the winter had higher absorbtivity.  相似文献   

9.
Current global climate models cannot resolve the complex topography over the Tibetan Plateau (TP) due to their coarse resolution. This study investigates the impacts of horizontal resolution on simulating aerosol and its direct radiative effect (DRE) over the TP by applying two horizontal resolutions of about 100 km and 25 km to the Chinese Academy of Sciences Flexible Global Ocean-Atmosphere Land System (CAS FGOALS-f3) over a 10-year period. Compared to the AErosol RObotic NETwork observations, a high-resolution model (HRM) can better reproduce the spatial distribution and seasonal cycles of aerosol optical depth (AOD) compared to a low-resolution model (LRM). The HRM bias and RMSE of AOD decreased by 0.08 and 0.12, and the correlation coefficient increased by 0.22 compared to the LRM. An LRM is not sufficient to reproduce the aerosol variations associated with fine-scale topographic forcing, such as in the eastern marginal region of the TP. The difference between hydrophilic aerosols in an HRM and LRM is caused by the divergence of the simulated relative humidity (RH). More reasonable distributions and variations of RH are conducive to simulating hydrophilic aerosols. An increase of the 10-m wind speed in winter by an HRM leads to increased dust emissions. The simulated aerosol DREs at the top of the atmosphere (TOA) and at the surface by the HRM are –0.76 W m–2 and –8.72 W m–2 over the TP, respectively. Both resolution models can capture the key feature that dust TOA DRE transitions from positive in spring to negative in the other seasons.  相似文献   

10.
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   

11.
人为气溶胶的直接辐射效应及其对南亚冬季风的影响   总被引:2,自引:0,他引:2  
运用区域气候模式RegCM4.0(Regional Climate Model Verson 4.0)耦合入一个化学过程,对硫酸盐、黑碳、有机碳这3种人为气溶胶的时空分布特征和直接辐射效应进行了数值模拟,进而研究了气溶胶对南亚冬季风的影响。结果表明:光学厚度和地表短波辐射强迫的时空变化可能主要受硫酸盐气溶胶的影响。在南亚夏季风向冬季风转换时期和南亚冬季风盛行时期,大气层顶和地表的负短波辐射强迫分布与气溶胶分布基本一致,地表辐射强迫强度绝对值比大气层顶辐射强迫强度绝对值大得多。相关分析和合成分析表明:在南亚夏季风向冬季风转换时期和南亚冬季风盛行时期,南亚人为气溶胶主要分布区中的气溶胶柱浓度含量与南亚冬季风的建立和强度有反相关关系。这与气溶胶吸收太阳辐射,从而引起气温和位势高度的变化有关。  相似文献   

12.
The aerosol optical properties and direct radiative forcing over the Mu Us desert of northern China, acquired through a CE318 sunphotometer of the ground-based Aerosol Robotic Network (AERONET), are analyzed. The seasonal variations in the aerosol optical properties are examined. The effect of meteorological elements (pressure, temperature, water vapor pressure, relative humidity and wind speed) on the aerosol optical properties is also studied. Then, the sources and optical properties under two different cases, a dust event and a pollution event, are compared. The results show that the high aerosol optical depth (AOD) found in Yulin was mostly attributed to the occurrence of dust events in spring from the Mu Us desert and deserts of West China and Mongolia, as well as the impacts of anthropogenic pollutant particles from the middle part of China in the other seasons. The seasonal variation and the probability distribution of the radiative forcing and the radiative forcing efficiency at the surface and the top of the atmosphere are analyzed and regressed using the linear and Gaussian regression methods.  相似文献   

13.
彭杰  张华 《大气科学学报》2015,38(4):465-472
结合Cloud Sat对云的主动观测和MODIS(MODerate-Resolution Imaging Spectroradiometer)对气溶胶的被动反演,研究了典型站点气溶胶对云的宏观、微观和辐射特性的影响。结果表明,气溶胶对大陆性和海洋性站点的云均有显著影响。1)随气溶胶光学厚度(Aerosol Optical Depth,AOD)增加,水汽含量较弱站点的低层(高层)云量呈减小(增加)趋势,而水汽条件较强站点的各层云量均增大,且具有较高(较低)云顶的云层发生概率在各个站点都呈增加(减小)趋势。2)AOD的增大导致各站点云滴和冰晶粒子的有效半径均减小、大气层顶的短波和长波云辐射强迫均增强、短波云辐射强迫绝对值的加强更显著、长波云辐射强迫增加的幅度相对更大。3)气象要素在AOD大(小)值情况下的变化表明,大尺度动力条件并不能解释云的上述特性随AOD的显著改变。  相似文献   

14.
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   

15.
A regional climate model is employed to simulate the aerosols(dust,sulfate,black carbon,and organic carbon) and their direct effect on the climate over China.The emphasis is on the direct radiative forcing due to the change in mixing state of aerosols.The results show that direct radiative forcing is significantly different between externally and internally mixed aerosols.At the top of the atmosphere(TOA),the radiative forcing of externally mixed aerosols is larger than that of internally mixed ones,especially in the Tarim desert region where the difference is about 0.7 W m 2.At the surface,however,the situation becomes opposite,especially in the Sichuan basin where the difference is about-1.4 W m 2.Nonetheless,either externally or internally mixed aerosols in China can result in a significant cooling effect,except for the warming in South China in winter and the slight warming in North China in February.The cooling effect induced by externally mixed aerosols is weaker than that induced by internally mixed aerosols,and this is more obvious in spring and winter than in summer and autumn.In spring and summer,the inhibiting effect of externally mixed aerosols on precipitation is less than that of internally mixed aerosols,whereas in autumn and winter the difference is not obvious.  相似文献   

16.
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.  相似文献   

17.
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   

18.
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   

19.
利用中分辨率光谱仪(MODIS)获得的气溶胶光学厚度(AOD)、细粒子比例(FMF)和臭氧检测仪(OMI)获得的气溶胶指数(AI)统计分析了2005—2014年我国华东地区气溶胶光学性质的时空分布特征,同时利用潜在源分析(PSCF)模型对我国华东地区AOD和AI的潜在源区进行分析。研究结果表明:华东地区的AOD、FMF和AI时空分布存在较大的差异,2005—2014年AOD和AI的平均值高值主要分布在华东地区北部,FMF的高值区则分布在华东南部地区;10 a间华东地区AOD呈现出先升高后降低的趋势,FMF波动幅度不明显,AI值有所上升;整个华东地区AOD的季节变化较为明显,春夏两季AOD明显高于秋冬两季。华东北部和中部地区夏季由于较高的相对湿度,AOD最大可达0.8以上。而在华东南部地区,夏季受到降水的影响,AOD维持在0.2~0.4之间。FMF季节变化趋势与AOD不同,夏季最大达到0.58,春季最小仅为0.26。AI平均值在冬季最大高达0.63,夏季最小,为0.27。PSCF分析显示华东地区AOD主要源区以局地排放为主,同时也存在由河南、湖北和湖南等周边省市近距离输送影响;AI以局地和北方远距离输送为主,同时也受到河南、湖北等周边省市近距离输送的影响。  相似文献   

20.
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   

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