Removal Processes of the Stratospheric SO <sub>2</sub> Volcanic Plume From the 2015 Calbuco Eruption

Abstract We analyze the volcanic plume from the April 2015 Calbuco eruption over a 35‐day period using simulations from Meso‐NH, a non‐hydrostatic mesoscale atmospheric model. A dedicated parameterization of the deep injection of the plume into the stratosphere ensures a realistic representation when compared to Infrared Atmospheric Sounding Interferometer satellite observations. During the first 12 hr of the eruption, on 22 April 2015, SO 2 mixing ratio reached 29 ppmv between 15 and 18 km for the first eruption pulse, and 38 ppmv between 12 and 16 km for the second. Most SO 2 was injected directly into the stratosphere, with a stratospheric load reaching 308 ktS (kilotons of atomic sulfur, i.e. 616 kilotons of SO 2 ) after the eruption. After 1 month, both stratospheric and tropospheric SO 2 loads returned to near‐background levels. During analysis, the chemical conversion of SO 2 into H 2 SO 4 removed a part of SO 2 from the stratosphere. During the long‐range advection, the co‐location between the subtropical jet stream and the Calbuco plume led to three significant stratospheric intrusions on 24, 26 and 28 April 2015. These events transferred stratospheric SO 2 into the troposphere, SO 2 mixing ratios in the upper troposphere reaching 15 ppmv, 26 and 15 ppbv, respectively. SO 2 is gradually oxidized into H 2 SO 4 , with up to 5 ktS of gaseous H 2 SO 4 in the stratosphere on 30 April, but dynamical processes dominate the SO 2 atmospheric budget over chemical transformations. This study demonstrates that stratospheric intrusions can play a critical role in the removal of volcanic material from the stratosphere following a major eruption.

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Journal
Journal of Geophysical Research Atmospheres
Published
2025-10-03
DOI
https://doi.org/10.1029/2025jd043850
Primary Topic
Atmospheric Ozone and Climate
Type
article
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article

Removal Processes of the Stratospheric SO 2 Volcanic Plume From the 2015 Calbuco Eruption

Pierre Tulet, Jean‐Luc Baray, François Gheusi, Valentin Duflot
Journal of Geophysical Research Atmospheres
Atmospheric Ozone and Climate
article

Removal Processes of the Stratospheric SO 2 Volcanic Plume From the 2015 Calbuco Eruption

Pierre Tulet, Jean‐Luc Baray, François Gheusi, Valentin Duflot
article en

Abstract

Abstract We analyze the volcanic plume from the April 2015 Calbuco eruption over a 35‐day period using simulations from Meso‐NH, a non‐hydrostatic mesoscale atmospheric model. A dedicated parameterization of the deep injection of the plume into the stratosphere ensures a realistic representation when compared to Infrared Atmospheric Sounding Interferometer satellite observations. During the first 12 hr of the eruption, on 22 April 2015, SO 2 mixing ratio reached 29 ppmv between 15 and 18 km for the first eruption pulse, and 38 ppmv between 12 and 16 km for the second. Most SO 2 was injected directly into the stratosphere, with a stratospheric load reaching 308 ktS (kilotons of atomic sulfur, i.e. 616 kilotons of SO 2 ) after the eruption. After 1 month, both stratospheric and tropospheric SO 2 loads returned to near‐background levels. During analysis, the chemical conversion of SO 2 into H 2 SO 4 removed a part of SO 2 from the stratosphere. During the long‐range advection, the co‐location between the subtropical jet stream and the Calbuco plume led to three significant stratospheric intrusions on 24, 26 and 28 April 2015. These events transferred stratospheric SO 2 into the troposphere, SO 2 mixing ratios in the upper troposphere reaching 15 ppmv, 26 and 15 ppbv, respectively. SO 2 is gradually oxidized into H 2 SO 4 , with up to 5 ktS of gaseous H 2 SO 4 in the stratosphere on 30 April, but dynamical processes dominate the SO 2 atmospheric budget over chemical transformations. This study demonstrates that stratospheric intrusions can play a critical role in the removal of volcanic material from the stratosphere following a major eruption.

Journal of Geophysical Research AtmospheresVol. 130(19)
Centre National de la Recherche Scientifique (FR), Université Clermont Auvergne (FR), Laboratoire d'Aérologie (FR), Laboratoire de Météorologie Physique (FR), Institut de Recherche pour le Développement (FR), NILU (NO)
Openalex Percentile: Top 68%
Atmospheric Ozone and Climate
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