The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate

Globally, carbonyl sulphide (COS) is the most abundant sulphur gas in the atmosphere. Our chemistry-climate model (CCM) of the lower and middle atmosphere with aerosol module realistically simulates the background stratospheric sulphur cycle, as observed by satellites in volcanically quiescent perio...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Brühl, C., Lelieveld, J., Crutzen, P. J., Tost, H.
Format: Other/Unknown Material
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/acp-12-1239-2012
https://www.atmos-chem-phys.net/12/1239/2012/
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spelling ftcopernicus:oai:publications.copernicus.org:acp11798 2023-05-15T16:39:20+02:00 The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate Brühl, C. Lelieveld, J. Crutzen, P. J. Tost, H. 2018-01-15 info:eu-repo/semantics/application/pdf https://doi.org/10.5194/acp-12-1239-2012 https://www.atmos-chem-phys.net/12/1239/2012/ eng eng info:eu-repo/grantAgreement/EC/FP7/226144 doi:10.5194/acp-12-1239-2012 https://www.atmos-chem-phys.net/12/1239/2012/ info:eu-repo/semantics/openAccess eISSN: 1680-7324 info:eu-repo/semantics/Text 2018 ftcopernicus https://doi.org/10.5194/acp-12-1239-2012 2019-12-24T09:56:25Z Globally, carbonyl sulphide (COS) is the most abundant sulphur gas in the atmosphere. Our chemistry-climate model (CCM) of the lower and middle atmosphere with aerosol module realistically simulates the background stratospheric sulphur cycle, as observed by satellites in volcanically quiescent periods. The model results indicate that upward transport of COS from the troposphere largely controls the sulphur budget and the aerosol loading of the background stratosphere. This differs from most previous studies which indicated that short-lived sulphur gases are also important. The model realistically simulates the modulation of the particulate and gaseous sulphur abundance in the stratosphere by the quasi-biennial oscillation (QBO). In the lowermost stratosphere organic carbon aerosol contributes significantly to extinction. Further, using a chemical radiative convective model and recent spectra, we compute that the direct radiative forcing efficiency by 1 kg of COS is 724 times that of 1 kg CO 2 . Considering an anthropogenic fraction of 30% (derived from ice core data), this translates into an overall direct radiative forcing by COS of 0.003 W m −2 . The direct global warming potentials of COS over time horizons of 20 and 100 yr are GWP(20 yr) = 97 and GWP(100 yr) = 27, respectively (by mass). Furthermore, stratospheric aerosol particles produced by the photolysis of COS (chemical feedback) contribute to a negative direct solar radiative forcing, which in the CCM amounts to −0.007 W m −2 at the top of the atmosphere for the anthropogenic fraction, more than two times the direct warming forcing of COS. Considering that the lifetime of COS is twice that of stratospheric aerosols the warming and cooling tendencies approximately cancel. Other/Unknown Material ice core Copernicus Publications: E-Journals Atmospheric Chemistry and Physics 12 3 1239 1253
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language English
description Globally, carbonyl sulphide (COS) is the most abundant sulphur gas in the atmosphere. Our chemistry-climate model (CCM) of the lower and middle atmosphere with aerosol module realistically simulates the background stratospheric sulphur cycle, as observed by satellites in volcanically quiescent periods. The model results indicate that upward transport of COS from the troposphere largely controls the sulphur budget and the aerosol loading of the background stratosphere. This differs from most previous studies which indicated that short-lived sulphur gases are also important. The model realistically simulates the modulation of the particulate and gaseous sulphur abundance in the stratosphere by the quasi-biennial oscillation (QBO). In the lowermost stratosphere organic carbon aerosol contributes significantly to extinction. Further, using a chemical radiative convective model and recent spectra, we compute that the direct radiative forcing efficiency by 1 kg of COS is 724 times that of 1 kg CO 2 . Considering an anthropogenic fraction of 30% (derived from ice core data), this translates into an overall direct radiative forcing by COS of 0.003 W m −2 . The direct global warming potentials of COS over time horizons of 20 and 100 yr are GWP(20 yr) = 97 and GWP(100 yr) = 27, respectively (by mass). Furthermore, stratospheric aerosol particles produced by the photolysis of COS (chemical feedback) contribute to a negative direct solar radiative forcing, which in the CCM amounts to −0.007 W m −2 at the top of the atmosphere for the anthropogenic fraction, more than two times the direct warming forcing of COS. Considering that the lifetime of COS is twice that of stratospheric aerosols the warming and cooling tendencies approximately cancel.
format Other/Unknown Material
author Brühl, C.
Lelieveld, J.
Crutzen, P. J.
Tost, H.
spellingShingle Brühl, C.
Lelieveld, J.
Crutzen, P. J.
Tost, H.
The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
author_facet Brühl, C.
Lelieveld, J.
Crutzen, P. J.
Tost, H.
author_sort Brühl, C.
title The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
title_short The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
title_full The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
title_fullStr The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
title_full_unstemmed The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
title_sort role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate
publishDate 2018
url https://doi.org/10.5194/acp-12-1239-2012
https://www.atmos-chem-phys.net/12/1239/2012/
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https://www.atmos-chem-phys.net/12/1239/2012/
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