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1.
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.  相似文献   

2.
In this paper, the RIEMS 2.0 model is used to simulate the distribution of sulfate, black carbon, and organic carbon aerosols over China (16.2°-44.1°N, 93.4°-132.4°E) in 1998. The climate effects of these three anthropogenic aerosols are also simulated. The results are summarized as follows: (1) The regional average column burdens of sulfate, BC, OC, and SOC were 5.9, 0.24, 2.4, and 0.49 mg m-2, with maxima of 33.9, 1.48, 7.3, and 1.1 mg m-2, respectively. The column burden and surface concentration of seco...  相似文献   

3.
The authors quantify the radiative effect of black carbon （BC） on simulated aerosol concentrations during the heavily polluted haze event of 11-14 January 2013 in northern China using the chemistry version of the Weather Research and Forecasting Model （WRF-Chem）. As a result of the stable synoptic conditions, simulated concentrations of BC and PM2.5 averaged over the study period were about 8-16 μg m-3 and 80-100 μg m-3, respectively, in the control simulation （CTRL）. When BC emissions were doubled （2BC）, tripled （3BC）, and quad- rupled （4BC） relative to the CTRL run, the simulated concentrations of aerosols in different regions showed distinct changes. The radiative effect of BC was simulated to increase concentrations of aerosols over Tianjin （Doml） and southern Henan （Dora3）, but to decrease in southern Hebei （Dora2）. Relative to the CTRL simulation, concen- trations of PM2s over Doml, Dom2, and Dom3 were simulated in 4BC to change by ＋18.6 1μg m-3 （＋32.3%）, -5.7 μg m 3 （-7.3%）, and ＋7.2 μg m3 （＋12.6%）, respec- tively. The BC-induced increases in aerosol concentra- tions corresponded mainly to the reductions in planetary boundary layer height over Doml and Dom3. The reduc- tions of aerosol concentrations in Dora2 were mainly caused by the weakened wind convergence at 850 hPa and reduced concentrations of sulfate and nitrate associ- ated with the reduced surface-layer ozone levels and rela- tive humidity.  相似文献   

4.
The direct climatic effect of aerosols for the 1980-2000 period over East Asia was numerically investigated by a regional scale coupled climate-chemistry/aerosol model,which includes major anthropogenic aerosols(sulfate,black carbon,and organic carbon) and natural aerosols(soil dust and sea salt) .Anthropogenic emissions used in model simulation are from a global emission inventory prepared for the Intergovernmental Panel on Climate Change Fifth Assessment Report(IPCC AR5) ,whereas natural aerosols are calculated online in the model.The simulated 20-year average direct solar radiative effect due to aerosols at the surface was estimated to be in a range of-9--33 W m-2 over most areas of China,with maxima over the Gobi desert of West China,and-12 W m-2 to-24 W m-2 over the Sichuan Basin,the middle and lower reaches of the Yellow River and the Yangtze River.Aerosols caused surface cooling in most areas of East Asia,with maxima of-0.8-C to-1.6-C over the deserts of West China,the Sichuan Basin,portions of central China,and the middle reaches of the Yangtze River. Aerosols induced a precipitation decrease over almost the entire East China,with maxima of-90 mm/year to-150 mm/year over the Sichuan Basin,the middle reaches of the Yangtze River and the lower reaches of the Yellow River.Interdecadal variation of the climate response to the aerosol direct radiative effect is evident,indicating larger decrease in surface air temperature and stronger perturbation to precipitation in the 1990s than that in the 1980s,which could be due to the interdecadal variation of anthropogenic emissions.  相似文献   

5.
In this study the authors apply the chemistry version of the Weather Research and Forecasting model （WRF-Chem） to examine the impacts of black carbon （BC）-induced changes in snow albedo on simulated temperature and precipitation during the severe snowstorm that occurred in southern China during 0800 26 January to 0800 29 January 2008 （Note that all times are local time except when otherwise stated）. Black carbon aerosol was simulated online within the WRF-Chem. The model resuits showed that surface-albedo, averaged over 27-28 January, can be reduced by up to 10% by the deposition of BC. As a result, relative to a simulation that does not consider deposition of BC on snow/ice, the authors predicted surface air temperatures during 27-28 January can differ by -1.95 to 2.70 K, and the authors predicted accumulated precipitation over 27-28 January can differ by -2.91 to 3.10 mm over Areas A and B with large BC deposition. Different signs of changes are determined by the feedback of clouds and by the availability of water vapor in the atmosphere.  相似文献   

6.
Anthropogenic emission inventory for aerosols and reactive gases is crucial to the estimation of aerosol radiative forcing and climate effects.Here,the anthropogenic emission inventory for AerChemMIP,endorsed by CMIP6,is briefly introduced.The CMIP6 inventory is compared with a country-level inventory(i.e.,MEIC)over China from 1986 to 2015.Discrepancies are found in the yearly trends of the two inventories,especially after 2006.The yearly trends of the aerosol burdens simulated by CESM2 using the two inventories follow their emission trends and deviate after the mid-2000s,while the simulated aerosol optical depths(AODs)show similar trends.The difference between the simulated AODs is much smaller than the difference between model and observation.Although the simulated AODs agree with the MODIS satellite retrievals for country-wide average,the good agreement is an offset between the underestimation in eastern China and the overestimation in western China.Low-biased precursor gas of SO2,overly strong convergence of the wind field,overly strong dilution and transport by summer monsoon circulation,too much wet scavenging by precipitation,and overly weak aerosol swelling due to low-biased relative humidity are suggested to be responsible for the underestimated AOD in eastern China.This indicates that the influence of the emission inventory uncertainties on simulated aerosol properties can be overwhelmed by model biases of meteorology and aerosol processes.It is necessary for climate models to perform reasonably well in the dynamical,physical,and chemical processes that would influence aerosol simulations.  相似文献   

7.
This study estimates direct radiative forcing by tropospheric ozone and all aerosols between the years 1850 and 2000, using the new IPCC AR5 （the Intergovernmental Panel on Climate Change Fifth Assessment Report） emissions inventories and a fully coupled chemistry-aerosol general circulation model. As compared to the previous Global Emissions Inventory Activity （GEIA） data, that have been commonly used for forcing estimates since 1990, the IPCC AR5 emissions inventories report lower anthropogenic emissions of organic carbon and black carbon aerosols and higher sulfur and NOx emissions. The simulated global and annual mean burdens of sulfate, nitrate, black carbon （BC）, primary organic aerosol （POA）, secondary organic aerosol （SOA）, and ozone were 0.79, 0.35, 0.05, 0.49, 0.34, and 269 Tg, respectively, in the year 1850, and 1.90, 0.90, 0.11, 0.71, 0.32, and 377 Tg, respectively, in the year 2000. The estimated annual mean top of the atmosphere （TOA） direct radiative forcing of all anthropogenic aerosols based on the AR5 emissions inventories is -0.60 W m^-2 on a global mean basis from 1850 to 2000. However, this is -2.40 W m-2 when forcing values are averaged over eastern China （18-45°N and 95-125°E）. The value for tropospheric ozone is 0.17 W m^-1 on a global mean basis and 0.24 W m^-2 over eastern China. Forcing values indicate that the climatic effect of aerosols over eastern China is much more significant than the globally averaged effect.  相似文献   

8.
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.  相似文献   

9.
The chemistry version of the Weather Research and Forecasting model (WRF/Chem) was coupled with the anthropogenic emission inventory of David Streets to investigate the impacts of secondary aerosols on a persistent fog event from 25 to 26 October 2007, in Northern China. The spatial distribution of the simulated fog is consistent with satellite observations, and the time-height distributions of the simulated boundary layer where the fog formed are also in good agreement with these observations. The sensitivity studies show that the secondary aerosols of SO 4 , NO 3 , and NH 4 formed from gaseous precursors of SO 2 , NO x , and NH 3 had substantial impacts on the formation processes and microphysical structure of the fog event. The decrease of the secondary aerosols obviously reduced the liquid water path and column droplet number concentration of the fog below the 1-km layer, and the corresponding area-averaged liquid water path and droplet number concentration of the fog decreased by 43% and 79%, respectively. The concentrations of NO x and NO 3 were found to be extremely high in this case. The concentration of interstitial aerosol NO 3 was much higher than the SO 4 and NH 4 , but the concentration of SO 4 was highest in the cloud-borne aerosols. The average activation ratios for SO 4 , NO 3 , and NH 4 were 34%, 31%, and 30%, respectively, and the maximum ratios reached 62%, 86%, and 55% during the fog episode.  相似文献   

10.
The Regional Integrated Environmental Model System(RIEMS 2.0) coupled with a chemistry-aerosol model and the Princeton Ocean Model(POM) is employed to simulate regional oceanic impact on atmospheric circulation and the direct radiative effect(DRE) of aerosol over East Asia.The aerosols considered in this study include both major anthropogenic aerosols(e.g.,sulfate,black carbon,and organic carbon) and natural aerosols(e.g.,soil dust and sea salt) .The RIEMS 2.0 is driven by NCEP/NCAR reanalysis II,and the simulated period is from 1 January to 31 December 2006.The results show the following:(1) The simulated annual mean sea-level pressure by RIEMS 2.0 with POM is lower than without POM over the mainland and higher without POM over the ocean.(2) In summer,the subtropical high simulated by RIEMS 2.0 with POM is stronger and extends further westward,and the continental low is stronger than without POM in summer.(3) The aerosol optical depth(AOD) simulated by RIEMS 2.0 with POM is larger in the middle and lower reaches of the Yangtze River than without POM.(4) The direct radiative effect with POM is stronger than that without POM in the middle and lower reaches of the Yangtze River and parts of southern China. Therefore,the authors should take account of the impact of the regional ocean model on studying the direct climate effect of aerosols in long term simulation.  相似文献   

11.
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   

12.
Future global emissions of aerosols will play an important role in governing the nature and magnitude of future anthropogenic climate change. We present in this paper a number of future scenarios of emissions of black carbon (BC) and organic carbon (OC) by world region, which we combine with sulfate (SO4) assessed in terms of the emissions of its precursor, SO2. We find that aerosol emissions from the household and industrial sectors are likely to decline along almost all future pathways. Transportation emissions, however, are subject to complex interacting forces that can lead to either increases or decreases. Biomass burning declines in many scenarios, but the Amazon rainforests remain vulnerable if unsustainable economic growth persists. East Asia is the key region for primary aerosols, and trends in China will have a major bearing on the direction and magnitude of releases of BC (expected reductions in the range of 640–1290 Gg), OC (reductions of 520–1900 Gg), and SO2 (ranging from an increase of 21 Tg to a reduction of 30 Tg). Analysis of joint BC, OC, and SO2 emission changes identifies a number of key world regions and economic sectors that could be effectively targeted for aerosol reductions.  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.
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850 hPa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。  相似文献   

15.
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.  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   

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