Variability of NO<sub>x</sub> in the polar middle atmosphere from October 2003 to March 2004: vertical transport vs. local production by energetic particles

We use NO, NO<sub>2</sub> and CO from MIPAS/ENVISAT to investigate the impact of energetic particle precipitation onto the NO<sub>x</sub> budget from the stratosphere to the lower mesosphere in the period from October 2003 to March 2004, a time of high solar and geomagnetic a...

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Bibliographic Details
Main Authors: M. Sinnhuber, B. Funke, T. von Clarmann, M. Lopez-Puertas, G. P. Stiller, A. Seppälä
Format: Article
Language:English
Published: Copernicus Publications 2014-07-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/14/7681/2014/acp-14-7681-2014.pdf
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Summary:We use NO, NO<sub>2</sub> and CO from MIPAS/ENVISAT to investigate the impact of energetic particle precipitation onto the NO<sub>x</sub> budget from the stratosphere to the lower mesosphere in the period from October 2003 to March 2004, a time of high solar and geomagnetic activity. We find that in the winter hemisphere the indirect effect of auroral electron precipitation due to downwelling of upper mesospheric/lower thermospheric air into the stratosphere prevails. Its effect exceeds even the direct impact of the very large solar proton event in October/November 2003 by nearly 1 order of magnitude. Correlations of NO<sub>x</sub> and CO show that the unprecedented high NO<sub>x</sub> values observed in the Northern Hemisphere lower mesosphere and upper stratosphere in late January and early February are fully consistent with transport from the upper mesosphere/lower thermosphere and subsequent mixing at lower altitudes. In the polar summer Southern Hemisphere, we observed an enhanced variability of NO and NO<sub>2</sub> on days with enhanced geomagnetic activity, but this seems to indicate enhanced instrument noise rather than a direct increase due to electron precipitation. A direct effect of electron precipitation onto NO<sub>x</sub> can not be ruled out, but, if any, it is lower than 3 ppbv in the altitude range 40–56 km and lower than 6 ppbv in the altitude range 56–64 km. An additional significant source of NO<sub>x</sub> due to local production by precipitating electrons below 70 km exceeding several parts per billion as discussed in previous publications appears unlikely.
ISSN:1680-7316
1680-7324