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Isotopic studies of ice core nitrate and atmospheric nitrogen oxides in polar regions.

机译:极区冰芯硝酸盐和大气氮氧化物的同位素研究。

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摘要

Atmospheric nitrogen oxides regulate concentrations of natural and anthropogenic trace gases through interactions with tropospheric oxidants. Understanding past and present changes in atmospheric NOx (NO + NO2) is possible through measurements of nitrate (NO3- or nitric acid, HNO3) in polar ice cores. This dissertation is comprised of four studies which contribute towards understanding the controls on nitrate isotopes preserved in polar ice.;Box modeling of local photochemistry at Summit, Greenland show that the delta 15N and delta18O of HNO3 are influenced by several factors, including isotope fractionation associated with NO-NO 2 cycling and seasonal changes in HNO3 formation chemistry and in NOx sources. A technique for the capture of atmospheric NO2 in remote regions for later isotopic analysis is described. First measurements of the delta15N of NO2 at Summit show little difference with the delta15N of HNO3, indicating that isotope fractionation associated with the oxidation of NO 2 to HNO3 is small.;The role of post-depositional processing on nitrate isotopes in the Summit snowpack is explored through isotopic measurements of gas-phase HNO3 , surface snow nitrate, and snowpit nitrate. These measurements indicate that NOx emitted from the snow following nitrate photolysis quickly recombines with local oxidants to produce HNO3 prior to recycling back to the snow. This photolytic loss and recycling has a small influence on nitrate isotopes preserved in ice at Summit.;Measurements of nitrate isotopes in an ice core from South Pole, Antarctica show evidence of active post-depositional recycling and loss of nitrate. A large near-surface trend in the delta15N of nitrate is attributed to post-depositional losses, while the delta18O of nitrate indicates that oxygen isotope fractionation associated with post-depositional loss is overwhelmed by the influence of local oxidants on nitrate recycling.;The concentration and delta15N of nitrate in an ice core from Summit, Greenland exhibit trends which are strongly correlated with recent changes in global NOx emissions. The Greenland delta 15N record indicates that the delta15N of recent NOx emissions must be isotopically light, which is consistent with the combustion of fossil fuels. This shows that the Greenland delta 15N record preserves changes in source emissions of atmospheric NO x.
机译:大气氮氧化物通过与对流层氧化剂相互作用来调节自然和人为痕量气体的浓度。通过测量极性冰芯中的硝酸盐(NO3-或硝酸,HNO3),可以了解大气中NOx(NO + NO2)的过去和现在的变化。本论文包括四项研究,这些研究有助于了解极地冰中硝酸盐同位素的控制方法。格陵兰萨米特峰的局部光化学盒模型表明,HNO3的δ15N和δ18O受多种因素影响,包括相关的同位素分馏NO-NO 2循环以及HNO3形成化学和NOx来源的季节性变化。描述了一种用于捕获偏远地区大气中的NO2以便随后进行同位素分析的技术。在Summit上对NO2的delta15N进行的首次测量显示与HNO3的delta15N差异不大,这表明与NO 2氧化为HNO3相关的同位素分馏很小。通过同位素测量气相HNO3,地表硝酸硝酸盐和雪坑硝酸盐进行了探索。这些测量结果表明,硝酸盐光解后从雪中散发出的NOx会迅速与局部氧化剂重新结合,生成HNO3,然后再循环回雪中。这种光解损失和回收利用对在Summit上保存在冰中的硝酸盐同位素影响很小。;对南极南极冰芯中硝酸盐同位素的测量表明,有活跃的沉积后回收利用和硝酸盐损失的证据。硝酸盐δ15N的较大的近地表趋势归因于沉积后的损失,而硝酸盐的δ18O表明与沉积后损失有关的氧同位素分馏被局部氧化剂对硝酸盐循环利用的影响所淹没。格陵兰岛萨米特市冰芯中硝酸盐的δ15N和δ15N的变化趋势与近期全球NOx排放变化密切相关。格陵兰三角洲15N记录表明,最近的NOx排放量的δ15N必须是同位素轻的,这与化石燃料的燃烧是一致的。这表明格陵兰三角洲15N记录保留了大气中NOx排放源的变化。

著录项

  • 作者

    Jarvis, Julia C.;

  • 作者单位

    University of Washington.;

  • 授予单位 University of Washington.;
  • 学科 Biogeochemistry.;Atmospheric Sciences.;Geochemistry.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 134 p.
  • 总页数 134
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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