Deactivation of N2A Σumolecules in the aurora

Recent rocket observations of the N₂ V-K (Vegard-Kaplan) system in the aurora have been reinterpreted using an atmospheric model based on mass spectrometer measurements in an aurora of similar intensity at the same time of year. In contrast to the original interpretation, we find that population by cascade from the C³Π_u and B³Π_g states in the A³Σ_u⁺v=0,1 levels, as calculated using recently measured electron excitation cross sections, accurately accounts for the observed relative emission rates (IV-K/12PG_0.0). In addition there is no need to change the production rate of A ³ Σ _u⁺ molecules relative to that of C³Π_uv=0 as a function of altitude in order to fit the profile of the deactivation probability to the atmospheric model. Quenching of A ³ Σ _u⁺ molecules at high altitudes is dominated by atomic oxygen. The rate constants for the v=0 and v=1 levels are 8 × 10^?11 cm³ sec^?1 and 1.7 × 10^?10 cm³ sec^?1 respectively, as determined using the model atmosphere mentioned above. Recent observations with a helium cooled mass spectrometer suggest that conventional mass spectrometer measurements tend to underestimate the atomic oxygen relative concentration. The rate coefficients may therefore be too large by as much as a factor of 3. Below 130 Km we find that it is possible to account for the deactivation in bright auroras by invoking large nitric oxide concentrations, similar to those recently observed mass spectrometrically and using a rate constant of 8 × 10^?11 cm³ sec^?1 for both the v=1 levels. This rate constant is very nearly the same as that measured in the laboratory (7 × 10^?11 cm³ sec^?1). Molecular oxygen appears not to play a significant role in deactivating the lower A ³ Σ _u⁺ levels.