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首页> 外文期刊>Atmospheric chemistry and physics >Impacts of biogenic and anthropogenic emissions on summertime ozone formation in the Guanzhong Basin, China
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Impacts of biogenic and anthropogenic emissions on summertime ozone formation in the Guanzhong Basin, China

机译:生物学和人为排放对中国广州盆地夏季臭氧形成的影响

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摘要

This study is the first attempt to understand the synergistic impact of anthropogenic and biogenic emissions on summertime ozone (O-3) formation in the Guanzhong (GZ) Basin where Xi'an, the oldest and the most populous city (with a population of 9 million) in northwestern China, is located. Month-long (August 2011) WRF-Chem simulations with different sensitivity experiments were conducted and compared with near-surface measurements. Biogenic volatile organic compounds (VOCs) concentrations was characterized from six surface sites among the Qinling Mountains, and urban air composition was measured in Xi'an city at a tower 100ma.s. The WRF-Chem control experiment reasonably reproduced the magnitudes and variations of observed O-3, VOCs, NOx, PM2.5, and meteorological parameters, with normalized mean biases for each parameter within +/- 21 %. Subsequent analysis employed the factor separation approach (FSA) to quantitatively disentangle the pure and synergistic impacts of anthropogenic and/or biogenic sources on summertime O-3 formation. The impact of anthropogenic sources alone was found to be dominant for O-3 formation. Although anthropogenic particles reduced NO2 photolysis by up to 60 %, the anthropogenic sources contributed 19.1 ppb O-3 formation on average for urban Xi'an. The abundant biogenic VOCs from the nearby forests promoted O-3 formation in urban areas by interacting with the anthropogenic NOx. The calculated synergistic contribution (from both biogenic and anthropogenic sources) was up to 14.4 ppb in urban Xi'an, peaking in the afternoon. Our study reveals that the synergistic impact of individual source contributions to O-3 formation should be considered in the formation of air pollution control strategies, especially for big cities in the vicinity of forests.
机译:本研究首次试图了解人为臭氧和生物发射对夏季臭氧(O-3)盆地的协同影响,其中最古老,最古老的城市(人口9人)百万)在中国西北部,位于。月长(2011年8月)对具有不同敏感性实验的WRF-Chem模拟,并与近表面测量进行比较。生物挥发性有机化合物(VOCS)浓度的特征在于秦岭六个表面位点,在塔100mA的西安市测量城市空气组合物。 WRF-Chem控制实验合理地再现了观察到的O-3,VOC,NOx,PM2.5和气象参数的幅度和变化,具有常规的平均偏差为+/- 21%内的每个参数。随后的分析采用因子分离方法(FSA)来定量解除人为和/或生物源对夏季O-3形成的纯粹和协同影响。仅发现人为源的影响是O-3形成的占主导地位。虽然人为颗粒的光解降低了60%,但是人为源的平均贡献了19.1 ppb o-3形成。附近森林的丰富生物转霉通过与人为NOx相互作用,促进了城市地区的O-3形成。计算的协同贡献(来自生物和人为)在Xi'an城市达到14.4 ppb,下午达到峰值。我们的研究表明,应考虑在形成空气污染控制策略中的单个来源对O-3形成的协同影响,特别是对于森林附近的大城市。

著录项

  • 来源
    《Atmospheric chemistry and physics》 |2018年第2期|共19页
  • 作者单位

    Nanjing Univ Informat Sci &

    Technol Jiangsu Key Lab Atmospher Environm Monitoring &

    C Jiangsu Collaborat Innovat Ctr Atmospher Environm Sch Environm Sci &

    Engn Nanjing 210044 Jiangsu Peoples R China;

    Chinese Acad Sci Inst Earth Environm SKLLQG Key Lab Aerosol Chem &

    Phys Xian 710061 Shaanxi Peoples R China;

    Natl Ctr Atmospher Res POB 3000 Boulder CO 80307 USA;

    Univ Calif Irvine Dept Earth Syst Sci Irvine CA 92697 USA;

    Nanjing Univ Informat Sci &

    Technol Jiangsu Key Lab Atmospher Environm Monitoring &

    C Jiangsu Collaborat Innovat Ctr Atmospher Environm Sch Environm Sci &

    Engn Nanjing 210044 Jiangsu Peoples R China;

    Chinese Acad Sci Inst Earth Environm SKLLQG Key Lab Aerosol Chem &

    Phys Xian 710061 Shaanxi Peoples R China;

    Univ Iowa Dept Chem &

    Biochem Engn Ctr Global &

    Reg Environm Res Iowa City IA 52242 USA;

    Nanjing Univ Informat Sci &

    Technol Jiangsu Key Lab Atmospher Environm Monitoring &

    C Jiangsu Collaborat Innovat Ctr Atmospher Environm Sch Environm Sci &

    Engn Nanjing 210044 Jiangsu Peoples R China;

    Chinese Acad Sci Inst Earth Environm SKLLQG Key Lab Aerosol Chem &

    Phys Xian 710061 Shaanxi Peoples R China;

    Tsinghua Univ Dept Earth Syst Sci Beijing 100084 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 大气科学(气象学);
  • 关键词

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