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首页> 外文期刊>Atmospheric chemistry and physics >Historical (1850–2000) gridded anthropogenic and biomass burning emissions of reactive gases and aerosols: methodology and application
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Historical (1850–2000) gridded anthropogenic and biomass burning emissions of reactive gases and aerosols: methodology and application

机译:历史(1850–2000年)的网格化人为和生物质燃烧产生的活性气体和气溶胶的排放:方法和应用

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摘要

We present and discuss a new dataset of gridded emissions covering the historical period (1850–2000) in decadal increments at a horizontal resolution of 0.5 in latitude and longitude. The primary purpose of this inventory is to provide consistent gridded emissions of reactive gases and aerosols for use in chemistry model simulations needed by climate models for the Climate Model Intercomparison Program #5 (CMIP5) in support of the Intergovernmental Panel on Climate Change (IPCC) Fifth Assessment report (AR5). Our best estimate for the year 2000 inventory represents a combination of existing regional and global inventories to capture the best information available at this point; 40 regions and 12 sectors are used to combine the various sources. The historical reconstruction of each emitted compound, for each region and sector, is then forced to agree with our 2000 estimate, ensuring continuity between past and 2000 emissions. Simulations from two chemistry-climate models are used to test the ability of the emission dataset described here to capture long-term changes in atmospheric ozone, carbon monoxide and aerosol distributions. The simulated long-term change in the Northern mid-latitudes surface and mid-troposphere ozone is not quite as rapid as observed. However, stations outside this latitude band show much better agreement in both present-day and long-term trend. The model simulations indicate that the concentration of carbon monoxide is underestimated at the Mace Head station; however, the long-term trend over the limited observational period seems to be reasonably well captured. The simulated sulfate and black carbon deposition over Greenland is in very good agreement with the ice-core observations spanning the simulation period. Finally, aerosol optical depth and additional aerosol diagnostics are shown to be in good agreement with previously published estimates and observations.
机译:我们提出并讨论了一个网格排放的新数据集,该数据涵盖了历史时期(1850–2000年),以十年为增量,纬度和经度的水平分辨率为0.5。该清单的主要目的是为政府间气候变化专门委员会(IPCC)提供气候模型比对计划#5(CMIP5)所需的化学模型模拟中使用的化学气体模型和模拟气体,以提供一致的网格排放。第五次评估报告(AR5)。我们对2000年库存的最佳估计是现有区域和全球库存的结合,以获取此时的最佳信息。 40个地区和12个部门用于合并各种来源。然后,每个区域和部门的每种排放化合物的历史重建都必须与我们的2000年估算相一致,以确保过去和2000年排放之间的连续性。来自两个化学-气候模型的模拟用于测试此处描述的排放数据集捕获大气臭氧,一氧化碳和气溶胶分布的长期变化的能力。在北中纬度地表和对流层中空臭氧的模拟长期变化并不像所观察到的那样快。但是,在当前和长期趋势中,此纬度范围以外的站点都显示出更好的一致性。模型仿真表明,梅斯总台站的一氧化碳浓度被低估了。但是,在有限的观察期内的长期趋势似乎可以很好地把握。格陵兰岛上的模拟硫酸盐和黑碳沉积与模拟期间的冰芯观测非常吻合。最后,显示的气溶胶光学深度和其他气溶胶诊断与先前发表的估计和观察结果非常吻合。

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