We present an analysis of the impact of heterogeneous chemistry on the partitioning of nitrogen species measured by the Upper Atmosphere Research Satellite (UARS) instruments. The UARS measurements utilized include N 2 O, HNO 3 , and ClONO 2 from the cryogenic limb array etalon spectrometer (CLAES), version 7 (v.7), and temperature, methane, ozone, H 2 O, HCl, NO and NO 2 from the halogen occultation experiment (HALOE), version 18. The analysis is carried out for the UARS data obtained between January 1992 and September 1994 in the 100‐ to 1‐mbar (∼17–47 km) altitude range and over 10° latitude bins from 70°S to 70°N. The spatiotemporal evolution of aerosol surface area density (SAD) is adopted from analysis of the Stratospheric Aerosol and Gas Experiment (SAGE) II data. A diurnal steady state photochemical box model, constrained by the temperature, ozone, H 2 O, CH 4 , aerosol SAD, and columns of O 2 and O 3 above the point of interest, has been used as the main tool to analyze these data. Total inorganic nitrogen (NO y ) is obtained by three different methods: (1) as a sum of the UARS‐measured NO, NO 2 , HNO 3 , and ClONO 2 ; (2) from the N 2 O‐NO y correlation, and (3) from the CH 4 ‐NO y correlation. To validate our current understanding of stratospheric heterogeneous chemistry for post‐Pinatubo conditions, the model‐calculated monthly averaged NO x /NO y ratios and the NO, NO 2 , and HNO 3 profiles are compared with the UARS‐derived data. In general, the UARS‐constrained box model captures the main features of nitrogen species partitioning in the post‐Pinatubo years, such as recovery of NO x after the eruption, their seasonal variability and vertical profiles. However, the model underestimates the NO 2 content, particularly in the 30‐ to 7‐mbar (∼23–32 km) range. Comparisons of the calculated temporal behavior of the partial columns of NO 2 and HNO 3 and ground‐based measurements at 45°S and 45°N are also presented. Our analysis indicates that ground‐based and HALOE v. 18 measurements of the NO 2 vertical columns are consistent within the range of their uncertainties and are systematically higher (up to 50%) than the model results at midlatitudes in both hemispheres. Reasonable agreement is obtained for HNO 3 columns at 45°S, suggesting some problems with nitrogen species partitioning in the model. Outstanding uncertainties are discussed.
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Danilin et al. (1999) studied this question.
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