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Photochemical Recovery

Important new observations have been obtained during the springtime recovery phases of the antarctic and arctic vortices. With simultaneous measurements of NO and ClO and a trajectory model, Schoeberl et al. [1993b] show that deactivation of reactive chlorine over the arctic occurs by fast photochemical formation of ClONO, at rates consistent with decomposition of HNO into NO by photolysis and by reaction with OH. This suggests that model treatments of OH abundances, which were not measured, are generally correct. Solomon and Keys [1992] and Keys et al. [1993] have shown that NO abundances increase in regions that still contain HNO. Within the ozone hole over Antarctica, however, ClO remains perturbed well into springtime. UARS observations of HNO, ClO, ClONO, and O complete the picture for Antarctica. Roche et al. [1994] and Santee et al. [1995] show a broad region where nitric acid has been completely removed, presumably by sedimentation of PSC particles earlier in the winter, as shown by lidar observations of Gobbi et al. [1991] and Deshler et al. [ 1991], and where there is little formation of ClONO. Thus, reactive chlorine is maintained at large abundances well into springtime and nearly all of the ozone is destroyed in about a month [ Anderson et al., 1991]. In this case, recovery of HCl via the Cl + CH reaction is more rapid than recovery of ClONO [ Liu et al., 1993], a situation that is opposite to that of the Arctic [ Webster et al., 1993a]. Outside of this denitrified region, nitric acid forms a ``collar'' around the ozone hole in mid- to late-winter in the same region that later exhibits a similar feature for ClONO, presumably as a result of photochemistry that is similar to that which occurs over most of the Arctic in spring [ Santee et al, 1995].



next up previous
Next: Ozone Loss: Observations Up: Polar Ozone Depletion Previous: Mid-Winter Chemistry



U.S. National Report to IUGG, 1991-1994
Rev. Geophys. Vol. 33 Suppl., © 1995 American Geophysical Union