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Annual variation and global distribution of strato-mesospheric carbon monoxide measured by ground-based Fourier Transform Infrared spectrometry

Authors :
Thorsten Warneke
Otto Schrems
Frank J. Murcray
Miriam Sinnhuber
Y. Kasai
I. Kramer
Nicholas B. Jones
Justus Notholt
T. Blumenstock
Stephen W. Wood
Voltaire A. Velazco
Frank Hase
Institute of Environmental Physics [Bremen] (IUP)
University of Bremen
National Institute of Water and Atmospheric Research [Auckland] (NIWA)
Institute for Meteorology and Climate Research (IMK)
Karlsruhe Institute of Technology (KIT)
School of Chemistry [Wollongong]
University of Wollongong [Australia]
Global Environment Division National Institute of Information and Communications Technology (NICT)
Department of Physics and Astronomy [Denver]
University of Denver
Department of Bentho-pelagic processes
Alfred-Wegener-Institut, Helmholtz-Zentrum für Polar- und Meeresforschung (AWI)
EGU, Publication
Source :
Atmospheric Chemistry and Physics Discussions, Atmospheric Chemistry and Physics Discussions, European Geosciences Union, 2006, 6 (4), pp.7119-7135, EPIC3Atmospheric chemistry and physics, 7, pp. 1305-1312
Publication Year :
2006
Publisher :
HAL CCSD, 2006.

Abstract

We present long-term time-series of strato-mesospheric CO vertical columns measured from stations located in Antarctica, mid-latitudes and the Arctic, covering the period from 1997–2005. The instrument and the measurement technique allows the separation of tropospheric and strato-mesospheric contributions to the CO column, therefore providing information on the chemistry and dynamics both at low and high altitudes. Data from polar stations show a similar annual variability of strato-mesospheric CO with a strong maximum in late winter and spring and a small enhancement in late summer for some stations, which we call the "summer bulge''. Generally, the mid-latitude stations show no significant annual variability of strato-mesospheric CO columns. Measurements were compared with a two-dimensional chemistry-transport model of the middle atmosphere. The annual and latitudinal variations of CO are reproduced very well by a model run including thermospheric CO. Comparison with different model scenarios show that the polar winter maximum is due solely to downward transport of thermospheric CO, while the summer maximum is due to CHOx chemistry in the stratosphere.

Details

Language :
English
ISSN :
16807367 and 16807375
Database :
OpenAIRE
Journal :
Atmospheric Chemistry and Physics Discussions, Atmospheric Chemistry and Physics Discussions, European Geosciences Union, 2006, 6 (4), pp.7119-7135, EPIC3Atmospheric chemistry and physics, 7, pp. 1305-1312
Accession number :
edsair.doi.dedup.....968b2204baec0f7548788d93da67e935