共查询到17条相似文献，搜索用时 109 毫秒
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.
东亚地区云和地表反照率对硫酸盐直接辐射强迫的影响 总被引：9，自引：3，他引：9
文中利用区域气候模式深入探讨了东亚地区云及地表反照率对硫酸盐直接辐射强迫的影响 ,同时定量估算了东亚地区云区气溶胶的直接辐射强迫 ,讨论了硫酸盐对地表和大气短波辐射平衡产生的不同影响。研究表明 :云对气溶胶的直接辐射强迫具有很强的减弱作用 ,这种减弱作用不仅取决于云覆盖份数 ,而且取决于云的光学厚度。就区域平均而言 ,文中模拟的东亚地区气溶胶直接辐射强迫为 - 0 .0 97W /m2 ,占总直接辐射强迫的 10 .4%左右。表明云对硫酸盐直接辐射具有很强的减弱作用 ,在估算其总的直接辐射强迫时 ,云区的贡献不可忽视。较高的地表反照率会减弱硫酸盐的直接辐射强迫 ,而较低地表反照率则会增加硫酸盐的辐射强迫。硫酸盐气溶胶对大气辐射平衡影响非常小 ,但对地表辐射平衡产生重要影响 ,影响程度与大气几乎一致。 相似文献
3.
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
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
4.
利用地面激光雷达、太阳光度计观测反演气溶胶光学特性参数,结合PM2.5观测数据,分析了2018年1月25—28日北京一次完整污染过程中气溶胶光学特性变化。基于观测数据,利用短波辐射传输模式计算了不同程度污染日,晴空背景下气溶胶对辐射加热率的改变程度。结果表明:清洁日（25日）,PM2.5日平均质量浓度为19.00 μg·m-3,440 nm气溶胶光学厚度为0.13,单次散射反照率为0.87,整层气溶胶消光系数低于0.10 km-1,短波辐射均为增温效应;污染期间（26—27日）,PM2.5日平均质量浓度为83.21 μg·m-3,气溶胶光学厚度为2.48,气溶胶散射能力增强,单次散射反照率达到0.94,气溶胶主要消光层厚度提升至3.00 km高度,消光系数平均值为0.43 km-1,气溶胶在垂直方向的变化导致气溶胶中上层（1.50~3.00 km高度）加热作用强烈,短波辐射加热率平均值达到13.89 K·d-1,而低层（1.50 km高度以内）加热作用较弱,加热率平均值仅为0.99 K·d-1。气溶胶散射能力增强导致加热作用减弱,污染日加热率对于气溶胶散射能力变化更敏感。 相似文献
5.
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
6.
基于国际大气化学-气候模式比较计划模式数据评估中国沙尘气溶胶直接辐射强迫 总被引：2，自引：0，他引：2
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
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
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.
利用多角度POLDER偏振资料实现陆地上空大气气溶胶光学厚度和地表反照率的同时反演 II. 实例分析 总被引：1，自引：0，他引：1
由于陆地地表反照率的复杂性,陆地上空气溶胶的反演一直是卫星对地观测的一个难点,针对这个难点,作者提出联合利用偏振反射率和总反射率提取陆地上空大气气溶胶光学厚度和地表反照率及其区域分布的反演方案,提出了利用NCEP资料订正由海拔高度引起的Rayleigh散射变化的具体方法,并利用POLDER（POLarization and Directionality of Earth's Reflectance）的LEVEL-1B资料进行实际反演计算,给出中国华北地区气溶胶光学厚度和地表反照率的区域分布。反演结果与地基观测进行了对比验证分析,结果表明,综合利用标量辐射和偏振信息的可以实现区域乃至全球尺度的大气气溶胶和地表反照率的定量反演。 相似文献
9.
基于SCIATRAN模型的二氧化氮DOAS 反演敏感性试验 总被引：6，自引：0，他引：6
气溶胶和地表反照率是影响星载SCIAMACHY仪器观测数据定量遥感NO2大气柱总量的2个主要因子.文中利用高光谱分辨率大气辐射传输模型SCIATRAN,在考虑分子吸收和气溶胶多次散射影响基础上,精确模拟了气溶胶、地表反照率和NO2气体浓度变化对差分处理前后卫星反射光谱的影响,并定义影响因子f,对3个模拟参数进行综合评价.结果表明:(1)通过剔除卫星反射光谱中慢变光谱变化成分,DOAS方法明显降低了气溶胶和地表反照率对卫星反射光谱的影响;(2)差分处理前,3个模拟参数的影响强弱依次为地表反照率、气溶胶和NO2浓度;而差分处理后,3个模拟参数的影响强弱依次为NO2浓度、地表反照率和气溶胶.在影响趋势上,气溶胶和地表反照率很相似,均体现为宽带效应,在440-450 nm内有水汽强吸收和多次散射复杂相互作用导致的较大峰值;NO2浓度变化对差分处理前后的光谱都呈现气体吸收结构的影响特性;(3)由于吸收和散射相互作用等因素的影响,在基于卫星观测的差分光谱中仍然残留有气溶胶和地表反照率的误差,地表反照率约占18.6%,气溶胶约占6.2%.因此,当前SCIAMACHY遥感的NO2产品在中国区域浓度偏高,需要对气溶胶和地表反照率进行二次精细化的订正. 相似文献
10.
浑善达克沙地沙尘气溶胶的辐射强迫 总被引：5，自引：7，他引：5
利用2001年春季浑善达克沙地外场观测的辐射资料及大气辐射模式,对沙尘气溶胶的局地辐射强迫进行了分析和模拟估算。计算结果表明,浑善达克沙地大气透过率日变化显著,晴天可达0.80以上,沙尘天气最低在0.01以下;白天沙尘的辐射强迫对地表有冷却作用,夜间起保温作用。观测期间,平均大气透过率为0.6,白天沙尘对地面向下长波辐射的平均强迫增加量为16.76 W.m-2,对地面净辐射能收支的平均强迫减少量为62.76 W.m-2;夜间地表长波辐射净损失量因沙尘作用减少,平均为67.84 W.m-2。 相似文献
11.
Muhammad Ali Salman Tariq Khalid Mahmood Asim Daud Adila Batool Zia-ul-Haq 《Asia-Pacific Journal of Atmospheric Sciences》2014,50(2):153-162
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
12.
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
13.
利用区域气候模式RegCM3模拟2000年我国黑碳气溶胶的分布特征和辐射强迫。结果表明,黑碳气溶胶主要分布在我国黄河以南、青藏高原以东的广大区域,柱含量由南向北递减;柱含量最大值在0.6mg／m^2以上,出现在中南、四川盆地、湖南、贵州、广西、广东西部和云南南部等地区;青藏高原南侧黑碳气溶胶次高值区的存在,反映了气溶胶的跨国界输送并影响区域气候的特点。黑碳气溶胶的大气顶辐射强迫介于0.1—0.8w／m^2之间,地表辐射强迫介于-0.1— -2.0W／m^2之间,两者分布特征与柱含量分布特征基本一致。同柱含量相似,黑碳气溶胶大气顸辐射强迫和地表辐射强迫也有明显的季节性变化,春季最大,秋、冬季次之,夏季最小。 相似文献
14.
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
15.
Yunfei FU Jiachen ZHU Yuanjian YANG Renmin YUAN Guosheng LIU Tao XIAN Peng LIU 《大气科学进展》2017,34(8):952-964
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
16.
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. 相似文献
17.
基于太湖地区MFRSR遥感大气气溶胶光学特性和大气污染状况 总被引：1，自引：1，他引：0
利用2008年5月16日至2009年4月17日太湖地区多光谱旋转遮光辐射仪（multi—filter ro—tating shadow—band radiometer,简称MFRSR）的观测资料进行反演,得出415、500、615、675和870nm5个波段大气气溶胶光学厚度（aerosol optical depth,简称AOD）及各季节浑浊度系数和波长指数的统计结果。结果表明,5个波段AOD的最大值分别为1．9、1．6、1．3、1．2和1．0;它们谱分布的半宽度分别为0．90、0．70、0．55、0．45和0．25;AOD频率分布极大值处所对应的AOD值分别为0．750、0．550、0．475、0．425和0．425。5个波段AOD的平均值在春季最大,夏季次之,除870nm外,均为冬季最小。浑浊度系数变化范围为0～1．25,其中大于0．2的占97％以上,大于0．4的占66％以上。春季、夏季、秋季和冬季的波长指数变化范围分别为0～3．0、0～2．8、0．2～2．0和0．2～2．0,表明太湖地区大气污染较为严重,且受人为源的影响显著。相对于秋冬季,春夏季有较大粒径的气溶胶粒子存在。 相似文献