nerc.ac.uk

Oxygen isotope mass balance of atmospheric nitrate at Dome C, East Antarctica, during the OPALE campaign

Savarino, J.; Vicars, W.C.; Legrand, M.; Preunkert, S.; Jourdain, B.; Frey, M.M. ORCID: https://orcid.org/0000-0003-0535-0416; Kukui, A.; Caillon, N.; Gil Roca, J.. 2016 Oxygen isotope mass balance of atmospheric nitrate at Dome C, East Antarctica, during the OPALE campaign. Atmospheric Chemistry and Physics, 16. 2659-2673. https://doi.org/10.5194/acp-16-2659-2016

Before downloading, please read NORA policies.
[img]
Preview
Text
Savarino.pdf - Published Version
Available under License Creative Commons Attribution.

Download (649kB) | Preview

Abstract/Summary

Variations in the stable oxygen isotope composition of atmospheric nitrate act as novel tools for studying oxidative processes taking place in the troposphere. They provide both qualitative and quantitative constraints on the pathways determining the fate of atmospheric nitrogen oxides (NO + NO2 = NOx). The unique and distinctive 17O-excess (Δ17O = δ17O − 0.52 × δ18O) of ozone, which is transferred to NOx via oxidation, is a particularly useful isotopic fingerprint in studies of NOx transformations. Constraining the propagation of 17O-excess within the NOx cycle is critical in polar areas where there exists the possibility of extending atmospheric investigations to the glacial/interglacial time scale using deep ice core records of nitrate. Here we present measurements of the comprehensive isotopic composition of atmospheric nitrate collected at Dome C (East Antarctic plateau) during the austral summer of 2011/12. Nitrate isotope analysis has been here combined for the first time with key precursors involved in nitrate production (NOx, O3, OH, HO2, RO2, etc.) and direct observations of the transferrable Δ17O of surface ozone, which was measured at Dome C throughout 2012 using our recently developed analytical approach. Assuming that nitrate is mainly produced in Antarctica in summer through the OH + NO2 pathway and using concurrent measurements of OH and NO2, we calculated a Δ17O signature for nitrate in the order of (21–22 ± 3) ‰. These values are lower than the measured values that ranged between 27 and 31 ‰. This discrepancy between expected and observed Δ17O(NO3−) values suggests the existence of an unknown process that contributes significantly to the atmospheric nitrate budget over this east Antarctic region.

Item Type: Publication - Article
Digital Object Identifier (DOI): https://doi.org/10.5194/acp-16-2659-2016
Programmes: BAS Programmes > BAS Programmes 2015 > Atmosphere, Ice and Climate
ISSN: 1680-7316
Date made live: 23 Sep 2015 13:20 +0 (UTC)
URI: https://nora.nerc.ac.uk/id/eprint/511164

Actions (login required)

View Item View Item

Document Downloads

Downloads for past 30 days

Downloads per month over past year

More statistics for this item...