Constraining the propagation of the 17O-excess of ozone in the troposphere : Towards a quantitative interpretation of the oxygen isotopic composition of atmospheric nitrate

The unique and distinctive 17O-excess (Δ17O) of ozone (O3) serves as a valuable tracer for oxidative processes in both modern and ancient atmospheres. This isotopic signature is propagated throughout the atmospheric reactive nitrogen (NOx = NO + NO2) cycle and preserved in nitrate (NO3-) aerosols an...

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Bibliographic Details
Main Author: Vicars, William
Other Authors: Laboratoire de glaciologie et géophysique de l'environnement (LGGE), Observatoire des Sciences de l'Univers de Grenoble (OSUG), Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut national des sciences de l'Univers (INSU - CNRS)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Université Savoie Mont Blanc (USMB Université de Savoie Université de Chambéry )-Centre National de la Recherche Scientifique (CNRS)-Université Joseph Fourier - Grenoble 1 (UJF)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut national des sciences de l'Univers (INSU - CNRS)-Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA)-Université Savoie Mont Blanc (USMB Université de Savoie Université de Chambéry )-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Université de Grenoble, Joël Savarino
Format: Doctoral or Postdoctoral Thesis
Language:French
Published: HAL CCSD 2013
Subjects:
Online Access:https://theses.hal.science/tel-00856960
https://theses.hal.science/tel-00856960v2/document
https://theses.hal.science/tel-00856960v2/file/pdf2star-1397485622-34090_VICARS_2013_archivage.pdf
Description
Summary:The unique and distinctive 17O-excess (Δ17O) of ozone (O3) serves as a valuable tracer for oxidative processes in both modern and ancient atmospheres. This isotopic signature is propagated throughout the atmospheric reactive nitrogen (NOx = NO + NO2) cycle and preserved in nitrate (NO3-) aerosols and mineral deposits, providing a conservative tracer for the relative importance of ozone and other key oxidants involved in NOx cycling. However, despite the intense research effort dedicated to the interpretation of Δ17O(NO3-) measurements, the atmospheric processes responsible for the transfer of Δ17O to nitrate and their overall influence on nitrate isotopic composition on different spatial and temporal scales are not well understood. Furthermore, due to the inherent complexity of extracting ozone from ambient air, the absolute magnitude and spatiotemporal variability of Δ17O(O3) remains poorly constrained, a problem that has confounded the interpretation of Δ17O measurements for over a decade. The research questions that have been pursued in this thesis were formulated to address these knowledge gaps. The primary analytical tool used was the bacterial denitrifier method followed by continuous-flow isotope ratio mass spectrometry (CF-IRMS), which allows for the comprehensive isotopic analysis of nitrate (i.e., δ15N, δ18O, Δ17O). This method was applied to the isotopic analysis of nitrate samples in two case studies: (i) an investigation of the diurnal and spatial features of atmospheric nitrate isotopic composition in coastal California; and (ii) a study of the seasonality and air-snow transfer of nitrate stable isotopes on the Antarctic plateau. Furthermore, the method was adapted to the isotopic characterization of ozone via chemical conversion of its terminal oxygen atoms to nitrate. During the course of this thesis, a large dataset of tropospheric Δ17O(O3) measurements has been obtained, including a full annual record from Grenoble, France (45 °N) and a ship-based latitudinal profile from 50 °S to 50 °N in the ...