河北省气溶胶标高时空变化及其成因

Simulation of Temporal and Spatial Variations and Causes of Aerosol Scale Height in Hebei Province

  • 摘要: 以2012年河北省20个监测站的MODIS AOD(气溶胶光学厚度)和近地面水平能见度数据为基础,应用Peterson 模型和高斯模型,计算气溶胶标高月均值年内变化模型系数;应用全微分近似计算原理,构建了气溶胶标高时空变化的成因模型.结果表明:①全省平均气溶胶标高以夏季最高,为3.298 km;春、秋季次之,分别为2.864和2.284 km;冬季最低,为1.597 km. 全省气溶胶标高空间分布以夏季地域差异最显著,最大值为3.193 km;冬季地域差异最小,最大值为1.487 km. ②在全省尺度上,大气颗粒物排放强度和大气边界层高度每变化1%时,将会引致气溶胶标高分别变化0.577%和0.143%,二者对气溶胶标高变化的贡献率分别为80.1%和19.9%;在省内6个次级区域尺度上,大气颗粒物排放强度越大的区域,大气边界层高度对气溶胶标高的贡献率越大,如冀中南平原、沧州沿海平原和冀东平原的贡献率分别达到63.7%、57.8%、54.2%;反之则贡献率较低,如冀中平原、冀西北山区和冀东北山区的贡献率则分别仅为45.4%、32.6%、8.6%.

     

    Abstract: On the assumption that aerosol concentration decreases exponentially with the increase of height, aerosol scale height can reflect the characteristic thickness of aerosols in the atmospheric boundary layer. In the present study, using Peterson and Gauss modeling, regression models of monthly mean aerosol scale height changes over time were fitted based on MODIS satellite-retrieved aerosol optical depth (AOD) data and near-ground visibility data at 20 stations in Hebei Province in 2012. Distribution maps of the average aerosol scale heights over the year 2012 and in the four seasons in Hebei Province were determined using Kriging interpolation. A generic model of temporal and spatial variations of the aerosol scale height was constructed based on the principle of total differential approximate calculation. The results showed that the highest aerosol scale height was 3.298 km in summer, while the lowest one was 1.597 km in winter. The aerosol scale heights were 2.864 km and 2.284 km in spring and autumn, respectively. The regional differences of spatial distribution of aerosol scale height were significant in summer, with the maximum regional difference being 3.193 km in summer. The regional differences were less significant in winter, with the maximum regional difference being 1.487 km in winter. At the provincial scale, when atmospheric particulate matter emission intensity and atmospheric boundary layer height changed 1%, aerosol scale height changed 0.577% and 0.143%, respectively. The relative contribution rates of the two factors to aerosol scale height were 80.1% and 19.9%, respectively. Atmospheric particulate matter emission intensity was the main contributor to spatial and temporal variations of aerosol scale height. At the regional scale of Hebei Province, where atmospheric particulate matter emissions intensity was greater, the contribution of atmospheric boundary layer height to aerosol scale height was greater, especially in the Central South Hebei Plain (63.7%), Cangzhou Coastal Plain (57.8%) and Eastern Hebei Plain (54.2%). Meanwhile, the contribution of atmospheric boundary layer height to aerosol scale height was smaller when atmospheric particulate matter emissions intensity was small, especially in the Central Hebei Plain (45.4%), Northwest Hebei Mountains (32.6%) and Northeast Hebei Mountains (8.6%).

     

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