Atmospheric nitrogen oxides (NO and NO2) at Dome C, East Antarctica, during the OPALE campaign

Frey, M. M., Roscoe, H. K., Kukui, A., Savarino, J., France, J. L., King, M. D., Legrand, M. and Preunkert, S. (2015) Atmospheric nitrogen oxides (NO and NO2) at Dome C, East Antarctica, during the OPALE campaign. Atmospheric Chemistry and Physics, 15 (14). pp. 7859-7875. ISSN 1680-7324

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Abstract

Mixing ratios of the atmospheric nitrogen oxides NO and NO2 were measured as part of the OPALE (Oxidant Production in Antarctic Lands & Export) campaign at Dome C, East Antarctica (75.1 degrees S, 123.3 degrees E, 3233 m), during December 2011 to January 2012. Profiles of NOx mixing ratios of the lower 100m of the atmosphere confirm that, in contrast to the South Pole, air chemistry at Dome C is strongly influenced by large diurnal cycles in solar irradiance and a sudden collapse of the atmospheric boundary layer in the early evening. Depth profiles of mixing ratios in firn air suggest that the upper snowpack at Dome C holds a significant reservoir of photolytically produced NO2 and is a sink of gas-phase ozone (O-3). First-time observations of bromine oxide (BrO) at Dome C show that mixing ratios of BrO near the ground are low, certainly less than 5 pptv, with higher levels in the free troposphere. Assuming steady state, observed mixing ratios of BrO and RO2 radicals are too low to explain the large NO2 : NO ratios found in ambient air, possibly indicating the existence of an unknown process contributing to the atmospheric chemistry of reactive nitrogen above the Antarctic Plateau. During 2011-2012, NOx mixing ratios and flux were larger than in 2009-2010, consistent with also larger surface O-3 mixing ratios resulting from increased net O-3 production. Large NOx mixing ratios at Dome C arise from a combination of continuous sunlight, shallow mixing height and significant NOx emissions by surface snow (F-NOx). During 23 December 2011-12 January 2012, median F-NOx was twice that during the same period in 20092010 due to significantly larger atmospheric turbulence and a slightly stronger snowpack source. A tripling of F-NOx in December 2011 was largely due to changes in snowpack source strength caused primarily by changes in NO3- concentrations in the snow skin layer, and only to a secondary order by decrease of total column O-3 and associated increase in NO3- photolysis rates. A source of uncertainty in model estimates of F-NOx is the quantum yield of NO3- photolysis in natural snow, which may change over time as the snow ages.

Item Type:	Article
Additional Information:	© Author(s) 2015. This work is distributed under the Creative Commons Attribution 3.0 License.
Uncontrolled Keywords:	boundary-layer,south-pole,radiative-transfer,reactive nitrogen,photochemical production,tropospheric bro,snow emissions,plateau,nitrate,surface
Faculty \ School:	Faculty of Science > School of Environmental Sciences
Depositing User:	Pure Connector
Date Deposited:	13 Nov 2015 17:01
Last Modified:	22 Oct 2022 00:25
URI:	https://ueaeprints.uea.ac.uk/id/eprint/55263
DOI:	10.5194/acp-15-7859-2015

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