中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Evaluation of preindustrial to present-day black carbon and its albedo forcing from Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

文献类型:期刊论文

作者McConnell, JR (McConnell, J. R.)[ 7 ]; Ming, J (Ming, J.)[ 13 ]; Myhre, G (Myhre, G.)[ 5 ]; Nagashima, T (Nagashima, T.)[ 14 ]; Naik, V (Naik, V.)[ 15 ]; Lee, YH (Lee, Y. H.)[ 1,2 ]; Lamarque, JF (Lamarque, J. -F.)[ 3 ]; Rumbold, ST (Rumbold, S. T.)[ 9 ]; Skeie, RB (Skeie, R. B.)[ 14 ]; Sudo, K (Sudo, K.)[ 16 ]
刊名ATMOSPHERIC CHEMISTRY AND PHYSICS
出版日期2013-03-05
卷号13期号:5页码:2607-2634
DOI10.5194/acp-13-2607-2013
文献子类期刊论文
英文摘要

As part of the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), we evaluate the historical black carbon (BC) aerosols simulated by 8 ACCMIP models against observations including 12 ice core records, long-term surface mass concentrations, and recent Arctic BC snowpack measurements. We also estimate BC albedo forcing by performing additional simulations using offline models with prescribed meteorology from 1996-2000. We evaluate the vertical profile of BC snow concentrations from these offline simulations using the recent BC snowpack measurements. Despite using the same BC emissions, the global BC burden differs by approximately a factor of 3 among models due to differences in aerosol removal parameterizations and simulated meteorology: 34 Gg to 103 Gg in 1850 and 82 Gg to 315 Gg in 2000. However, the global BC burden from preindustrial to present-day increases by 2.5-3 times with little variation among models, roughly matching the 2.5-fold increase in total BC emissions during the same period. We find a large divergence among models at both Northern Hemisphere (NH) and Southern Hemisphere (SH) high latitude regions for BC burden and at SH high latitude regions for deposition fluxes. The ACCMIP simulations match the observed BC surface mass concentrations well in Europe and North America except at Ispra. However, the models fail to predict the Arctic BC seasonality due to severe under-estimations during winter and spring. The simulated vertically resolved BC snow concentrations are, on average, within a factor of 2-3 of the BC snowpack measurements except for Greenland and the Arctic Ocean. For the ice core evaluation, models tend to adequately capture both the observed temporal trends and the magnitudes at Greenland sites. However, models fail to predict the decreasing trend of BC depositions/ice core concentrations from the 1950s to the 1970s in most Tibetan Plateau ice cores. The distinct temporal trend at the Tibetan Plateau ice cores indicates a strong influence from Western Europe, but the modeled BC increases in that period are consistent with the emission changes in Eastern Europe, the Middle East, South and East Asia. At the Alps site, the simulated BC suggests a strong influence from Europe, which agrees with the Alps ice core observations. At Zuoqiupu on the Tibetan Plateau, models successfully simulate the higher BC concentrations observed during the non-monsoon season compared to the monsoon season but overpredict BC in both seasons. Despite a large divergence in BC deposition at two Antarctic ice core sites, some models with a BC lifetime of less than 7 days are able to capture the observed concentrations. In 2000 relative to 1850, globally and annually averaged BC surface albedo forcing from the offline simulations ranges from 0.014 to 0.019 W m(-2) among the ACCMIP models. Comparing offline and online BC albedo forcings computed by some of the same models, we find that the global annual mean can vary by up to a factor of two because of different aerosol models or different BC-snow parameterizations and snow cover. The spatial distributions of the offline BC albedo forcing in 2000 show especially high BC forcing (i.e., over 0.1 W m(-2)) over Manchuria, Karakoram, and most of the Former USSR. Models predict the highest global annual mean BC forcing in 1980 rather than 2000, mostly driven by the high fossil fuel and biofuel emissions in the Former USSR in 1980.

语种英语
源URL[http://ir.ieecas.cn/handle/361006/9932]  
专题地球环境研究所_粉尘与环境研究室
通讯作者Lee, YH (Lee, Y. H.)[ 1,2 ]
作者单位1.Desert Research Institute, Nevada System of Higher Education, Reno, NV, USA;
2.Center for International Climate and Environmental Research Oslo (CICERO) and Department of Geosciences, University ofOslo, Oslo, Norway;
3.Department of Atmospheric, Oceanic and Space Sciences, University of Michigan, Ann Arbor MI, USA;
4.Key Laboratory of Tibetan Environment Changes and Land Surface Processes, Institute of Tibetan Plateau Research,Chinese Academy of Sciences, Beijing, China
5.F.A. Forel Institute, University of Geneva, Versoix, Switzerland;
6.Research Institute for Applied Mechanics, Kyushu University, Fukuoka, Japan;
7.Dept. of Earth and Environmental Science, Graduate School of Environmental Studies, Nagoya University, Nagoya, Japan;
8.NASA Goddard Institute for Space Studies and Columbia Earth Institute, New York, NY, USA;
9.National Center for Atmospheric Research (NCAR), Boulder, CO, USA;
10.UCAR/NOAA Geophysical Fluid Dynamics Laboratory, Princeton, NJ, USA;
推荐引用方式
GB/T 7714
McConnell, JR ,Ming, J ,Myhre, G ,et al. Evaluation of preindustrial to present-day black carbon and its albedo forcing from Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2013,13(5):2607-2634.
APA McConnell, JR .,Ming, J .,Myhre, G .,Nagashima, T .,Naik, V .,...&Horowitz, LW .(2013).Evaluation of preindustrial to present-day black carbon and its albedo forcing from Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP).ATMOSPHERIC CHEMISTRY AND PHYSICS,13(5),2607-2634.
MLA McConnell, JR ,et al."Evaluation of preindustrial to present-day black carbon and its albedo forcing from Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)".ATMOSPHERIC CHEMISTRY AND PHYSICS 13.5(2013):2607-2634.

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来源:地球环境研究所

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