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Ozone and its precursors over the United States: Sources, outflow, transpacific inflow, and hemispheric influence.

机译:臭氧及其在美国的前兆:来源,流出,跨太平洋流入和半球影响。

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摘要

This thesis examines the sources, outflow, and transpacific inflow of tropospheric ozone and its precursors in the United States using observations from two aircraft campaigns (ITCT-2K2, ICARTT) interpreted with a global three-dimensional chemical transport model (GEOS-Chem). We find a large springtime transpacific transport of Asian ozone plumes to the west coast of the United States in the free troposphere. Ozone production from the decomposition of peroxyacetylnitrate (PAN) during subsidence over the northeast Pacific represents a major and possibly dominant component of the ozone enhancement in these plumes. Strong dilution of Asian plumes, however, takes place during entrainment in the U.S. boundary layer, greatly reducing their impact at U.S. surface sites. California mountain sites are most sensitive to Asian pollution because of their exposure to the free troposphere. Extensive aircraft mapping of the U.S. boundary layer in summer confirms the recent decrease in nitrogen oxide (NOx) emissions required by recent regulation, and reveals a large overestimate of carbon monoxide (CO) emissions in current inventories. The model successfully simulates the export of anthropogenic NOx and its oxidation products, as well as the ozone-CO correlations in the U.S. boundary layer and its outflow, supporting previous model estimates of a large U.S. anthropogenic contribution to global tropospheric ozone through PAN export. However, the model greatly underestimates observed NOx in the upper troposphere, reflecting a higher-than-expected (factor of four) lightning source. This lightning source drives in turn a large ozone enhancement in the upper troposphere (>10 ppbv) with implications for radiative forcing and climate feedback through changes in lightning. Using the above constraints on ozone and its precursors we provide new estimates of North American anthropogenic, lightning, and biomass burning contributions to tropospheric ozone on the scale of the northern hemisphere.
机译:本文使用对两个飞机运动(ITCT-2K2,ICARTT)的观测结果进行了解释,研究了美国对流层臭氧及其前驱物的来源,流出和跨太平洋流入,并用全球三维化学迁移模型(GEOS-Chem)进行了解释。我们发现在自由对流层中,亚洲臭氧羽流向美国西海岸的春季大跨太平洋运输。在东北太平洋沉降过程中,过氧乙酰硝酸盐(PAN)分解产生的臭氧代表了这些羽流中臭氧增强的主要且可能是主要成分。但是,在美国边界层的夹带过程中,亚洲羽流被强烈稀释,大大降低了它们对美国地表的影响。加州山区对亚洲的污染最敏感,因为它们暴露在对流层中。夏季在美国边界层进行的广泛飞机制图证实了最近法规所要求的近期氮氧化物(NOx)排放量的减少,并揭示了当前清单中一氧化碳(CO)排放量的高估。该模型成功地模拟了人为NOx及其氧化产物的出口,以及美国边界层及其流出物中的臭氧与一氧化碳的相关性,从而支持了先前的模型估算,即通过PAN出口,美国对全球对流层臭氧的贡献很大。但是,该模型大大低估了对流层高层观测到的NOx,反映出比预期高(四倍)的雷源。这种雷源反过来又推动了对流层上层臭氧的大量增加(> 10 ppbv),这通过辐射的变化对辐射强迫和气候反馈产生了影响。利用上述对臭氧及其前驱物的限制,我们提供了北半球规模上北美人为,闪电和生物量燃烧对流层臭氧贡献的新估计。

著录项

  • 作者

    Hudman, Rynda Christina.;

  • 作者单位

    Harvard University.;

  • 授予单位 Harvard University.;
  • 学科 Atmospheric Sciences.; Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 117 p.
  • 总页数 117
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境污染及其防治;
  • 关键词

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