Aerosol and Clouds
Oxygen and sulfur isotopic composition of volcanic sulfate aerosol at the point of emission
Article first published online: 26 SEP 2006
DOI: 10.1029/2005JD006584
Copyright 2006 by the American Geophysical Union.
Issue
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Journal of Geophysical Research: Atmospheres (1984–2012)
Volume 111, Issue D18, 27 September 2006
Additional Information
How to Cite
, , , , , , , and (2006), Oxygen and sulfur isotopic composition of volcanic sulfate aerosol at the point of emission, J. Geophys. Res., 111, D18205, doi:10.1029/2005JD006584.
Publication History
- Issue published online: 26 SEP 2006
- Article first published online: 26 SEP 2006
- Manuscript Accepted: 22 JUN 2006
- Manuscript Revised: 8 JUN 2006
- Manuscript Received: 12 AUG 2005
Composition and Chemistry: Correction to “Oxygen and sulphur isotope composition of volcanic sulphate aerosol at the point of emission”
Vol. 112, Issue D9, Article first published online: 8 MAY 2007
Keywords:
- primary particles;
- volcanic degassing;
- sulfur cycle
[1] Volcanic sulfate aerosol is emitted from the vents of many active volcanoes, but its origin has not yet been explained. We report the first measurements of the isotopic compositions of near-vent volcanic aerosol sulfate and use the combined sulfur and oxygen isotope systematics of the aerosol and magma at Masaya volcano, Nicaragua, to draw preliminary conclusions about the production mechanism of near-source volcanic sulfate. The sulfate aerosol does not display a significant mass-independent oxygen or sulfur isotopic signature, which suggests that primary volcanic aerosol does not contribute to the larger mass-independent anomalies found in some ambient atmospheric aerosols and as preserved in ice cores. The oxygen isotope composition of the sulfate appeared to become heavier on the particle filters with increasing amount of sample collected and suggests that the δ18O value of the sulfate aerosol is <8‰. The sulfur isotopic composition of the sulfate did not vary with sample loading on the filters and had a mean δ34S value of 7.7 ± 0.8‰, similar to that of the magma (6.6 ± 0.2‰). The low Δ17O value, the δ18O value of the magma (6.6 ± 0.3‰) and the high δ18O value of atmospheric oxygen (23.5‰) suggest that known atmospheric oxidation pathways at ambient temperatures are not the major routes of production for this sulfate. Instead, the isotopic systematics of aerosol and magma are consistent with sulfate production either by high-temperature equilibration of the magmatic gas mixture with small amounts of atmospheric oxygen or by direct emission of SO42− from the magma.

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