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NO<sub><b><i>y</i></b></sub> partitioning and budget and its correlation with N<sub>2</sub>O in the Arctic vortex and in summer midlatitudes in 1997
56
Citations
50
References
2002
Year
Arctic EngineeringEngineeringAtmospheric PhotochemistrySummer MidlatitudesEarth System ScienceEarth ScienceNo YRegional Climate ResponseAtmospheric ScienceMicrometeorologyN 2StatisticsClimate ChangeClimate VariabilityHydrometeorologyMeteorologyAtmosphere Of EarthAtmospheric InteractionGeographyArctic VortexCryosphereKarlsruhe Simulation ModelClimate SystemClimate DynamicsClimatologyArctic StructureAtmospheric Process
Vertical profiles of the most important species of nocturnal total reactive nitrogen (NO y = NO 2 + HNO 3 + ClONO 2 + 2 N 2 O 5 + HO 2 NO 2 ) together with its source gas N 2 O were retrieved from infrared limb emission spectra measured by the Michelson Interferometer for Passive Atmospheric Sounding, Balloon‐borne version (MIPAS‐B) instrument inside the late winter arctic vortex from Kiruna (Sweden, 68°N) on 24 March 1997 and in summer midlatitudes from Gap (France, 44°N) on 2 July 1997. The measured data were compared to calculations performed with the three‐dimensional chemistry transport model (CTM) Karlsruhe Simulation model of the Middle Atmosphere (KASIMA). The results show that in the late winter arctic vortex most of the available nitrogen and chlorine is in the form of HNO 3 and ClONO 2 , respectively. An anomalous N 2 O‐NO y correlation observed in March 1997 appears to be caused to a large extent by quasi‐horizontal mixing of air masses across the vortex edge. However, near 20 km some denitrification of ∼1.5 to 2 ppbv NO y could be observed. The N 2 O profile measured in July 1997 indicates remnants of polar vortex air and is not reproduced by the CTM at the same location. However, the profile shapes of the individual compounds of the NO y family as well as the NO x /NO y ratio are reproduced fairly well by the model.
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