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首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >Spatial and temporal variations of aerosols around Beijing in summer 2006: 2. Local and column aerosol optical properties
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Spatial and temporal variations of aerosols around Beijing in summer 2006: 2. Local and column aerosol optical properties

机译:气溶胶的时空变化特征北京2006年夏季:2。气溶胶光学特性

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Model calculations were conducted using the Weather Research and Forecasting model coupled with chemistry (WRF-chem) for the region around Beijing, China, in the summer of 2006, when the CAREBeijing-2006 intensive campaign was conducted. In this paper, we interpret aerosol optical properties in terms of aerosol mass concentrations and their chemical compositions by linking model calculations with measurements. The model calculations generally captured the observed variability of various surface and column aerosol optical parameters in and around Beijing. At the surface, the spatial and temporal variations of aerosol absorption and scattering coefficients corresponded well to those of elemental carbon and sulfate mass concentrations, respectively, and were controlled by local-scale (<100 km and <24 hours) and regional-scale (<500 km and <3 days) emissions, respectively. The contribution of secondary aerosols and their water uptake increased with altitude within the planetary boundary layer. This variation led to a considerable increase in column aerosol optical depth and was responsible for the differences in regional and temporal variations between surface and column aerosol optical properties around Beijing. These processes are expected to be common in other megacity regions as well. Model calculations, however, underestimated or overestimated the absolute levels of aerosol optical properties in and around Beijing by up to 60%. Sensitivity studies showed that these discrepancies were mostly due to the uncertainties in aerosol mixing state and aerosol density (affecting mass extinction efficiency) in the model calculations. Good agreement with measurements is achieved when these aerosol properties are accurately predicted or assumed; however, significant bias can result when these properties are inadequately treated, even if total aerosol mass concentrations are reproduced well in the model calculations.
机译:使用的模型进行了计算气象研究和预测模型耦合与化学(WRF-chem)地区中国,北京,2006年的夏天,当carebeijing - 2006密集的运动进行的。气溶胶光学特性的质量浓度及其化学成分连接模型的计算和测量。模型计算一般了观察到各种表面和可变性列在气溶胶光学参数北京。气溶胶吸收和散射的变化系数对应的元素碳和硫酸质量浓度,分别是由局部范围控制(<和< 24小时100公里)和对地区级的核(< 500公里,< 3天)排放,分别。次生气溶胶和他们的贡献水吸收增加与高度内行星边界层。列气溶胶光学相当大的增加深度和负责的差异区域和时间变化之间的表面和列气溶胶光学特性北京。在其他的大城市地区。然而,计算低估或高估了气溶胶的绝对水平北京及周边地区的光学性质了60%。差异主要是由于不确定性在气溶胶混合状态和气溶胶密度(影响大规模灭绝的效率)模型计算。当这些气溶胶测量来实现属性是准确预测或假设;然而,重大偏差可以当这些结果属性是处理不当,即使总气溶胶质量浓度复制在模型计算。

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