Formaldehyde in summer

During the 2011/12 and 2012/13 austral summers, HCHO was investigated for the first time in ambient air, snow, and interstitial air at the Concordia site, located near Dome C on the East Antarctic Plateau, by deploying an Aerolaser AL-4021 analyzer. Snow emission fluxes were estimated from vertical...

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Veröffentlicht in:Atmospheric chemistry and physics 2015-06, Vol.15 (12), p.6689
Hauptverfasser: Preunkert, S, Legrand, M, Frey, M. M, Kukui, A, Savarino, J, Gallée, H, King, M, Jourdain, B, Vicars, W, Helmig, D
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Sprache:eng
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Zusammenfassung:During the 2011/12 and 2012/13 austral summers, HCHO was investigated for the first time in ambient air, snow, and interstitial air at the Concordia site, located near Dome C on the East Antarctic Plateau, by deploying an Aerolaser AL-4021 analyzer. Snow emission fluxes were estimated from vertical gradients of mixing ratios observed at 1 cm and 1 m above the snow surface as well as in interstitial air a few centimeters below the surface and in air just above the snowpack. Typical flux values range between 1 and 2 × 10.sup.12 molecules m.sup.-2 s.sup.-1 at night and 3 and 5 × 10.sup.12 molecules m.sup.-2 s.sup.-1 at noon. Shading experiments suggest that the photochemical HCHO production in the snowpack at Concordia remains negligible compared to temperature-driven air-snow exchanges. At 1 m above the snow surface, the observed mean mixing ratio of 130 pptv and its diurnal cycle characterized by a slight decrease around noon are quite well reproduced by 1-D simulations that include snow emissions and gas-phase methane oxidation chemistry. Simulations indicate that the gas-phase production from CH.sub.4 oxidation largely contributes (66%) to the observed HCHO mixing ratios. In addition, HCHO snow emissions account for ~ 30% at night and ~ 10% at noon to the observed HCHO levels.
ISSN:1680-7316
1680-7324