耦合气溶胶气候模式FGOALS-f3-L模拟青藏高原地区气溶胶特性（英文）

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.     

东亚地区人为气溶胶直接辐射强迫及其气候效应的数值模拟

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.     

全球不同类型气溶胶光学厚度的时空分布特征

利用MERRA-2(第2版现代研究与应用再分析)资料分析了1980-2017年全球硫酸盐、黑碳、有机碳、海盐、沙尘及总气溶胶光学厚度的时空分布特征;选取了北美、北非、南非、印度、中国和印度洋6个典型区域研究了硫酸盐、黑碳、有机碳、海盐和沙尘气溶胶对总气溶胶光学厚度的贡献率。结果表明,硫酸盐、黑碳、有机碳、海盐和沙尘气溶胶在全球非均匀分布,并且具有季节变化;全球总气溶胶的光学厚度(Aerosol Optical Depth,AOD)在夏季最大(0.137),春季次之(0.130),冬季最小(0.118);在6个典型区域里,北非地区总气溶胶的光学厚度最大,为0.43;其次是中国的东部地区,为0.41;每个区域其主要气溶胶的类型并不相同,在北美、中国东部及印度中部地区,硫酸盐是主导的气溶胶类型,贡献率分别为66%,63%和42%,在印度洋、南非及北非地区,海盐、有机碳和沙尘分别是最主要的气溶胶类型,贡献率分别为65%,51%和82%;对于黑碳、硫酸盐和总气溶胶,中国东部地区和印度中部地区有较为明显的增长趋势,其中总气溶胶光学厚度的线性增长率分别为0.007 a^-1和0.0056 a^-1,但在2010年以后,中国东部地区出现明显的下降。     

中国有机碳气溶胶时空分布与辐射强迫的模拟研究

利用区域气候模式RegCM3模拟研究2000年我国有机碳气溶胶的时空分布特征和辐射效应,得出以下结论:有机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,且柱含量由南向北递减;柱含量最大值可达3 mg/m2以上,出现在华南、中南、云贵、四川和西藏东南部。另外,柱含量分布有着明显的季节性,冬季最大,春季次之,夏季最小。在此基础上,本文还对有机碳气溶胶的柱含量时空分布变化的原因进行了分析。有机碳气溶胶在大气顶和地表均产生负的辐射强迫,其分布特征与柱含量分布特征基本一致,而且大气顶和地表的辐射强迫都具有明显的季节变化。模拟的大气顶辐射强迫在-0.1～-0.5 W/m2之间,与IPCC估计的有机碳气溶胶的辐射强迫数值-0.41 W/m2相当,说明区域气候模式RegCM3中有关有机碳气溶胶的参数化方案是比较合理的。     

人为气溶胶的直接辐射效应及其对南亚冬季风的影响

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。     

2006年中国地区大气气溶胶浓度分布特征的模拟研究

结合2006年最新的气溶胶排放源资料,以NCEP/NCAR再分析资料为气象场,驱动大气化学传输模式MATCH（Model of Atmospheric Transport and Chemistry）,模拟了2006年中国地区硫酸盐、黑碳和沙尘气溶胶的质量浓度分布及其季节变化。模拟的气溶胶光学厚度（AOD）结果与CSHNET观测网数据比较分析后发现,基于21个观测站的61组月平均数据与相应模拟结果的相关系数为0.63。模拟结果表明：2006年中国地区硫酸盐气溶胶高值区主要分布在中国的四川盆地、华北及长江流域等工业较发达地区,而且具有明显的季节变化,四川盆地及长江以南地区,硫酸盐气溶胶1月份浓度高于7月份,长江以北的大部分地区,7月份浓度高于1月份;黑碳气溶胶主要分布在黄河、长江中下游地区及华南等地区,1月份浓度高于7月份;沙尘气溶胶主要分布在内蒙古中部沙漠地区,4月份浓度最高,7月份次之,其他月份较少。     

中国黑碳气溶胶分布特征与辐射强迫的模拟研究

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。     

亚洲地区气溶胶及其对中国区域气候影响的数值模拟

使用一个耦合入化学过程的区域气候模式 (RegCM3), 在NCAR/NCEP再分析资料驱动下, 通过多年时间尺度的连续积分, 进行了亚洲区域气溶胶硫酸盐、 黑碳和有机碳的时空分布及其直接气候效应的数值模拟。首先对模式的模拟能力进行了检验, 结果表明, 模式能够较好地模拟中国地区气温和降水的分布, 对该区域气溶胶的时空分布有一定的模拟能力。模式模拟得到的气溶胶浓度分布在冬季南北差异较大而夏季较小。气溶胶浓度与其形成的大气层顶和地面负短波辐射强迫有较好的对应关系。四川盆地是气溶胶浓度及其产生的辐射强迫的高值区。气溶胶对地面气温和降水都产生影响。其中所引起的冬季气温降低, 与气溶胶的分布和浓度有一定的对应关系, 但夏季引起的降温中心位于河套及黄河下游地区。气溶胶使得冬季和夏季中国东部大部分地区的降水减少。同时, 对气温和降水上述变化的原因进行了讨论。     

近22a人为气溶胶对东亚地区夏季风环流影响的数值模拟研究

运用区域气候模式RegCM3耦合入一个化学过程,对东亚地区三类人为排放气溶胶（硫酸盐、黑碳和有机碳）的时空分布特征及其对夏季风环流的影响进行了数值模拟研究.模拟结果显示,气溶胶的引入会引起东亚地区夏季850 hPa风场发生改变,我国江淮以东洋面上空出现了一个气旋式距平环流中心,中心以西的偏北风气流将削弱东亚地区夏季西南季风.通过讨论春季中国地区气溶胶浓度与夏季东亚地区850 hPa经向风的时滞关系,以及夏季中国地区气溶胶浓度与同期东亚地区850 hPa经向风的关系,可以发现,春、夏季中国地区气溶胶浓度均与夏季东亚地区850hPa经向风有很好的负相关关系,当春季中国北方和夏季中国南方地区气溶胶浓度增加时,中国东部地区夏季偏南季风减弱.这可能与气溶胶改变了大气层顶和地表的辐射强迫,进而引起了海陆气压差异和位势高度场的变化有关.     

南京北郊黑碳气溶胶的浓度观测及辐射强迫研究

利用2008年南京大学浦口校区气溶胶采样数据对碳气溶胶的浓度变化特征进行了分析,建立了由气溶胶光学参量计算模块(OPAC)和辐射传输模型(TUV)组成的箱模式,并结合实际观测资料,利用该模式对南京北郊黑碳气溶胶的光学厚度及辐射强迫进行了评估。结果表明:南京北郊黑碳气溶胶(BC)的年平均浓度为6.7±4.6μg/m3,有机碳气溶胶(OC)的年平均浓度为21.3±13.3μg/m3,有机碳与黑碳气溶胶浓度的平均比值为3.4。黒碳气溶胶浓度具有夏季低、冬春季高的特点。由箱模式计算得到的黒碳气溶胶的年均光学厚度为0.07,年均吸收系数为44 Mm–1。白天正午晴空条件下黑碳所造成的最大瞬时地面辐射强迫可达-22.9±14.3 W/m2,在大气层顶造成的最大瞬时辐射强迫为12.5±7.3 W/m2。     

Aerosol characteristics over the Tibetan Plateau simulated with a coupled aerosol–climate model (FGOALS-f3-L) 耦合气溶胶气候模式FGOALS-f3-L模拟青藏高原地区气溶胶特性

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     

Characteristics of Anthropogenic Sulfate and Carbonaceous Aerosols over East Asia： Regional Modeling and Observation

The authors present spatial and temporal characteristics of anthropogenic sulfate and carbonaceous aerosols over East Asia using a 3-D coupled regional climate-chemistry-aerosol model, and compare the simulation with the limited aerosol observations over the region. The aerosol module consists of SO2, SO4^2-, hydrophobic and hydrophilic black carbon （BC） and organic carbon compounds （OC）, including emission, advections, dry and wet deposition, and chemical production and conversion. The simulated patterns of SO2 are closely tied to its emission rate, with sharp gradients between the highly polluted regions and more rural areas. Chemical conversion （especially in the aqueous phase） and dry deposition remove 60% and 30% of the total SO2 emission, respectively. The SO4^2- shows less horizontal gradient and seasonality than SO2, with wet deposition （60%） and export （27%） being two major sinks. Carbonaceous aerosols are spatially smoother than sulfur species. The aging process transforms more than 80% of hydrophobic BC and OC to hydrophilic components, which are removed by wet deposition （60%） and export （30%）. The simulated spatial and seasonal SO4^2-, BC and OC aerosol concentrations and total aerosol optical depth are generally consistent with the observations in rural areas over East Asia, with lower bias in simulated OC aerosols, likely due to the underestimation of anthropogenic OC emissions and missing treatment of secondary organic carbon. The results suggest that our model is a useful tool for characterizing the anthropogenic aerosol cycle and for assessing its potential climatic and environmental effects in future studies.     

非洲地区大气气溶胶光学厚度时空变化及亚速尔高压对沙尘越大西洋传输的影响

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。     

不同污染条件下气溶胶对短波辐射通量影响的模拟研究

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。      

Simulating Aerosol Optical Depth and Direct Radiative Effects over the Tibetan Plateau with a High-Resolution CAS FGOALS-f3 Model

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.     

Estimation of the Aerosol Radiative Effect over the Tibetan Plateau Based on the Latest CALIPSO Product

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.     

Assessment of Individual Direct Radiative Effects of Major Aerosol Species in East Asia

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.     

THE RADIATIVE EFFECTS OF ANTHROPOGENIC AEROSOLS OVER CHINA AND THEIR SENSITIVITY TO SOURCE EMISSION

In this paper,the RIEMS 2.0 model,source emission in 2006 and 2010 are used to simulate the distributions and radiative effects of different anthropogenic aerosols over China.The comparison between the results forced by source emissions in 2006 and 2010 also reveals the sensitivity of the radiative effects to source emission.The results are shown as follows:(1) Compared with those in 2006,the annual average surface concentration of sulfate in 2010 decreased over central and eastern China with a range of-5 to 0 μg/m~3;the decrease of annual average aerosol optical depth of sulfate over East China varied from 0.04 to 0.08;the annual average surface concentrations of BC,OC and nitrate increased over central and eastern China with maximums of 10.90,11.52 and 12.50μg/m~3,respectively;the annual aerosol optical depths of BC,OC and nitrate increased over some areas of East China with extremes of 0.006,0.007 and 0.008,respectively.(2)For the regional average results in 2010,the radiative forcings of sulfate,BC,OC,nitrate and their total net radiative forcing at the top of the atmosphere over central and eastern China were-0.64,0.29,-0.41,-0.33 and-1.1 W/m~2,respectively.Compared with those in 2006,the radiative forcings of BC and OC in 2010 were both enhanced,while that of sulfate and the net radiative forcing were both weakened over East China mostly.(3)The reduction of the cooling effect of sulfate in 2010 produced a warmer surface air temperature over central and eastern China;the maximum value was 0.25 K.The cooling effect of nitrate was also slightly weakened.The warming effect of BC was enhanced over most of the areas in China,while the cooling effect of OC was enhanced over the similar area,particularly the area between Yangtze and Huanghe Rivers.The net radiative effect of the four anthropogenic aerosols generated the annual average reduction and the maximum reduction were-0.096 and-0.285 K,respectively,for the surface temperature in 2006,while in 2010 they were-0.063 and-0.256 K,respectively.In summary,the change in source emission lowered the cooling effect of anthropogenic aerosols,mainly because of the enhanced warming effect of BC and weakened cooling effect of scattering aerosols.     

CAM5模式中两气溶胶模块的评估

公共大气模式 (CAM) 被广泛用于气候变化研究中,其5.0版中包含两个气溶胶模块MAM3和MOZART。利用AeroCom (2000年) 多模式中值、IMPROVE (1988—2005年) 和EMEP (2002—2008年) 站点资料对两模块进行了评估。结果表明:MAM3和MOZART模块都能很好地模拟硫酸盐气溶胶的季节变化, 与观测资料相比,模拟结果均在夏季偏高, 相关系数均在0.89左右,2倍误差内。两模块能较好地模拟黑碳气溶胶的时空分布特征, 与观测资料相比,模拟结果偏低,相关系数均在0.62左右, 排放源偏小而清除率偏大是造成黑碳气溶胶偏低的主要原因。两模块对有机碳气溶胶的模拟结果差别较大,大部分站点在3倍误差内,MAM3的结果偏高92.1%,MOZART则偏低58.1%;两模块一次有机碳的结果接近,差异主要源自对二次有机碳的模拟。两模块模拟的海盐气溶胶偏大,这主要是清除率偏小造成的。两模块采用相同的起沙机制,但起沙系数有差异, MAM3的沙尘源强偏大近两倍,模拟总量较大;MOZART的沙尘源强则偏低40%左右,模拟沙尘总量较低。即模式中气溶胶的输送和扩散过程偏弱,说明清除机制还有待改进。     

Present-day contribution of anthropogenic emissions from China to the global burden and radiative forcing of aerosol and ozone

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.