Please use this identifier to cite or link to this item: http://hdl.handle.net/2122/10297
AuthorsSurl, L.* 
Donohoue, D.* 
Aiuppa, A.* 
Bobrowski, N.* 
von Glasow, R.* 
TitleQuantification of the depletion of ozone in the plume of Mount Etna
Issue Date9-Mar-2015
Series/Report no./15(2015)
DOI10.5194/acp-15-2613-2015
URIhttp://hdl.handle.net/2122/10297
KeywordsMount Etna
Plume
depletion of ozone
Subject Classification04. Solid Earth::04.08. Volcanology::04.08.01. Gases 
AbstractVolcanoes are an important source of inorganic halogen species into the atmosphere. Chemical processing of these species generates oxidised, highly reactive, halogen species which catalyse considerable O3 destruction within volcanic plumes. A campaign of ground-based in situ O3, SO2 and meteorology measurements was undertaken at the summit of Mount Etna volcano in July/August 2012. At the same time, spectroscopic measurements were made of BrO and SO2 columns in the plume downwind. Depletions of ozone were seen at all in-plume measurement locations, with average O3 depletions ranging from 11–35 nmol mol􀀀1 (15–45 %). Atmospheric processing times of the plume were estimated to be between 1 and 4 min. A 1-D numerical model of early plume evolution was also used. It was found that in the early plume O3 was destroyed at an approximately constant rate relative to an inert plume tracer. This is ascribed to reactive halogen chemistry, and the data suggests the majority of the reactive halogen that destroys O3 in the early plume is generated within the crater, including a substantial proportion generated in a high-temperature “effective source region” immediately after emission. The model could approximately reproduce the main measured features of the ozone chemistry. Model results show a strong dependence of the near-vent bromine chemistry on the presence or absence of volcanic NOx emissions and suggest that near-vent ozone measurements can be used as a qualitative indicator of NOx emission.
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