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Coupling aerosol-cloud-radiative processes in the WRF-Chem model: Investigating the radiative impact of elevated point sources

机译:WRF-Chem模型中的气溶胶-云辐射过程耦合:研究高位点源的辐射影响

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The local and regional influence of elevated point sources on summertime aerosol forcing and cloud-aerosol interactions in northeastern North America was investigated using the WRF-Chem community model. The direct effects of aerosols on incoming solar radiation were simulated using existing modules to relate aerosol sizes and chemical composition to aerosol optical properties. Indirect effects were simulated by adding a prognostic treatment of cloud droplet number and adding modules that activate aerosol particles to form cloud droplets, simulate aqueous-phase chemistry, and tie a two-moment treatment of cloud water (cloud water mass and cloud droplet number) to precipitation and an existing radiation scheme. Fully interactive feedbacks thus were created within the modified model, with aerosols affecting cloud droplet number and cloud radiative properties, and clouds altering aerosol size and composition via aqueous processes, wet scavenging, and gas-phase-related photolytic processes. Comparisons of a baseline simulation with observations show that the model captured the general temporal cycle of aerosol optical depths (AODs) and produced clouds of comparable thickness to observations at approximately the proper times and places. The model overpredicted SO_2 mixing ratios and PM_(2.5) mass, but reproduced the range of observed SO_2 to sulfate aerosol ratios, suggesting that atmospheric oxidation processes leading to aerosol sulfate formation are captured in the model. The baseline simulation was compared to a sensitivity simulation in which all emissions at model levels above the surface layer were set to zero, thus removing stack emissions. Instantaneous, site-specific differences for aerosol and cloud related properties between the two simulations could be quite large, as removing abovesurface emission sources influenced when and where clouds formed within the modeling domain. When summed spa-tially over the finest resolution model domain (the extent of which corresponds to the typical size of a single global climate model grid cell) and temporally over a three day analysis period, total rainfall in the sensitivity simulation increased by 31% over that in the baseline simulation. Fewer optically thin clouds, arbitrarily defined as a cloud exhibiting an optical depth less than 1, formed in the sensitivity simulation. Domain-averaged AODs dropped from 0.46 in the baseline simulation to 0.38 in the sensitivity simulation. The overall net effect of additional aerosols attributable to primary particulates and aerosol precursors from point source emissions above the surface was a domain-averaged reduction of 5Wm~(-2) in mean daytime downwelling shortwave radiation.
机译:使用WRF-Chem社区模型研究了升高点源对北美东北部夏季气溶胶强迫和云气溶胶相互作用的局部和区域影响。使用现有模块模拟了气溶胶对入射太阳辐射的直接影响,以将气溶胶的尺寸和化学成分与气溶胶的光学特性相关联。通过添加云滴数量的预后处理和添加可激活气溶胶颗粒以形成云滴,模拟水相化学以及对云水进行两步处理(云水量和云滴数量)的模块来模拟间接影响。降水和现有的辐射方案。因此,在修改后的模型中创建了完全交互式的反馈,其中气溶胶影响着云滴的数量和云的辐射特性,而云则通过水相过程,湿式清除和气相相关的光解过程来改变气溶胶的大小和组成。基线模拟与观测值的比较表明,该模型捕获了气溶胶光学深度(AOD)的总体时间周期,并在大约适当的时间和地点产生了厚度与观测值相当的云。该模型高估了SO_2的混合比和PM_(2.5)的质量,但重现了观察到的SO_2与硫酸盐气溶胶比的范围,表明该模型中捕获了导致硫酸盐气溶胶形成的大气氧化过程。将基线模拟与灵敏度模拟进行了比较,在敏感性模拟中,表面层以上模型级别的所有排放均设置为零,从而消除了烟囱排放。两次模拟之间的气溶胶和云相关特性的瞬时,特定于现场的差异可能会很大,因为去除地表排放源会影响建模域内何时何地形成云。当在最高分辨率模型域上进行空间求和(范围的大小对应于单个全球气候模型网格单元的典型大小)并在三天的分析时间内进行时间求和时,灵敏度模拟中的总降雨量比过去增加了31%在基线模拟中。在灵敏度模拟中形成的光学上稀薄的云减少了,任意定义为光学深度小于1的云。域平均AOD从基线模拟中的0.46下降到灵敏度模拟中的0.38。来自地面上方点源排放的主要颗粒物和气溶胶前体所产生的额外气溶胶的总体净效应是,平均日间下行短波辐射的域平均降低5Wm〜(-2)。

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