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[1] We present an overview of the theoretical and algorithmic aspects of the Ozone Monitoring Instrument (OMI) aerosol and surface UV algorithms. Aerosol properties are derived from two independent algorithms. The nearUV algorithm makes use of OMI observations in the 350-390 nm spectral region to retrieve information on the absorption capacity of tropospheric aerosols. OMI-derived information on aerosol absorption includes the UV Aerosol Index and absorption optical depth at 388 nm. The other algorithm makes use of the full UV-to-visible OMI spectral coverage to derive spectral aerosol extinction optical depth. OMI surface UV products include erythemally weighted daily dose as well as erythemal dose rate and spectral UV irradiances calculated for local solar noon conditions. The advantages and limitations of the current algorithms are discussed, and a brief summary of several validation and evaluation analysis carried out to assess the current level of uncertainty of these products is presented.

Chemical ozone destruction occurs over both polar regions in local winter-spring. In the Antarctic, essentially complete removal of lower-stratospheric ozone currently results in an ozone hole every year, whereas in the Arctic, ozone loss is highly variable and has until now been much more limited. Here we demonstrate that chemical ozone destruction over the Arctic in early 2011 was--for the first time in the observational record--comparable to that in the Antarctic ozone hole. Unusually long-lasting cold conditions in the Arctic lower stratosphere led to persistent enhancement in ozone-destroying forms of chlorine and to unprecedented ozone loss, which exceeded 80 per cent over 18-20 kilometres altitude. Our results show that Arctic ozone holes are possible even with temperatures much milder than those in the Antarctic. We cannot at present predict when such severe Arctic ozone depletion may be matched or exceeded.