Chlorine monoxide in the Antarctic spring vortex: 1. Evolution of midday vertical profiles over McMurdo Station, 1993

We have obtained a prolonged record of emission spectra from chlorine monoxide in the vicinity of McMurdo Station, Antarctica, during formation of the austral spring ozone hole of 1993. These spectra have been processed to obtain vertical mixing ratio profiles by deconvolution of pressure-broadened line shapes. The resulting profiles give a detailed evolution for both altitude distribution and mixing ratio of ClO during development of a major ozone hole event. In early September, very strong emission was observed from pressure-broadened low-altitude ClO. Deconvolutions show that this came from an unusually thick layer, extending well above 20 km in altitude. This layer decreased steadily in thickness through September, accompanied by a shift of the peak mixing ratio from ∼21 km altitude in early September to ∼17–18 km by the end of the month, indicating an apparent descent rate of order 100 meters per day, although we argue that the true descent rate is probably lower than the apparent rate. A brief, significant decrease in ClO content occured in late September when the inner vortex edge (defined by the magnitude of Ertel's potential vorticity = 5.2·10−5 at ∼19–20 km) approached McMurdo, signifying that a strong gradient in ClO exists near the inner vortex edge. A rapid and apparently final deactivation of chlorine in the lower stratosphere was observed to start about October 1–2. The findings of initially large values of ClO well above 20 km are consistent with observation of polar stratospheric cloud formation in this range during the austral winter of 1993, and with observations showing increased ozone depletion above 20 km relative to previous years.

[1]  Stratospheric ClO profiles from McMurdo Station, Antarctica, spring 1992 , 1995 .

[2]  A. O'Neill,et al.  Mixing processes within the polar night jet , 1994 .

[3]  A. O'Neill,et al.  On the motion of air through the stratospheric polar vortex , 1994 .

[4]  P. Newman,et al.  Computations of diabatic descent in the stratospheric polar vortex , 1994 .

[5]  L. Emmons,et al.  Accuracy of profile retrievals from mm-wave spectra of ClO and N/sub 2/O , 1994, Proceedings of IGARSS '94 - 1994 IEEE International Geoscience and Remote Sensing Symposium.

[6]  Edward A. Cohen,et al.  Pressure broadening of ClO by N2 and O2 near 204 and 649 GHz and new frequency measurements between 632 and 725 GHz , 1994 .

[7]  W. H. Mallison,et al.  A new high-sensitivity superconducting receiver for mm-wave remote-sensing spectroscopy of the stratosphere , 1994 .

[8]  S. Oltmans,et al.  Record low ozone at the South Pole in the spring of 1993 , 1994 .

[9]  L. Froidevaux,et al.  MLS observations of lower stratospheric ClO and O3 in the 1992 Southern Hemisphere winter. [Microwave Limb Sounder] , 1993 .

[10]  P. Crutzen,et al.  On the potential importance of the gas phase reaction CH3O2 + ClO → ClOO + CH3O and the heterogeneous reaction HOCl + HCl → H2O + Cl2 in “ozone hole” chemistry , 1992 .

[11]  D. Toohey,et al.  Free Radicals Within the Antarctic Vortex: The Role of CFCs in Antarctic Ozone Loss , 1991, Science.

[12]  S. Solomon Progress towards a quantitative understanding of Antarctic ozone depletion , 1990, Nature.

[13]  W. Brune,et al.  In situ observations of BrO over Antarctica: ER‐2 aircraft results From 54°S to 72°S latitude , 1989 .

[14]  L. Emmons,et al.  New observations of a large concentration of ClO in the springtime lower stratosphere over Antarctica and its implications for ozone-depleting chemistry , 1989 .

[15]  P. Solomon,et al.  A ground-based technique for millimeter wave spectroscopic observations of stratospheric trace constituents , 1988 .

[16]  B. Connor,et al.  High concentrations of chlorine monoxide at low altitudes in the Antarctic spring stratosphere: diurnal variation , 1987, Nature.

[17]  S. Twomey,et al.  An extension to the Chahine method of inverting the radiative transfer equation. [application to ozone distribution in atmosphere] , 1977 .