Preprints
https://doi.org/10.5194/egusphere-2025-6033
https://doi.org/10.5194/egusphere-2025-6033
15 Jan 2026
 | 15 Jan 2026
Status: this preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).

Indirect climate forcing from ozone depleting substances

William J. Collins, John S. Daniel, Martyn P. Chipperfield, Martin Cussac, Makoto Deushi, Gregory Faluvegi, Paul Griffiths, Øivind Hodnebrog, Larry W. Horowitz, James Keeble, Douglas Kinnison, Vaishali Naik, Fiona M. O'Connor, Drew Shindell, Simone Tilmes, Kostas Tsigaridis, Zihao Wang, and James Weber

Abstract. Many halocarbons are powerful greenhouse gases and also influence climate indirectly through depletion of stratospheric ozone which opposes their direct greenhouse effect. Changes in effective radiative forcing (ERF) from historical ozone depletion have been diagnosed from model experiments with perturbed halocarbons run under the sixth Coupled Model Intercomparison Project. This is more negative than the offline stratospheric-temperature-adjusted radiative forcing (SARF). Including effects of ozone depletion on the methane lifetime makes the historical net ERF of ozone depleting substances consistent with zero. The Integrated Ozone Depletion (IOD) metric has been used to apportion this ERF between the halocarbon species and thereby derive indirect 100-year Global Warming Potentials (GWP100s) for a suite of halocarbons. The indirect GWP100 for CFC-11 is enough to make the net GWP100 likely negative, whereas the indirect contribution for CFC-12 is smaller due to a combination of longer stratospheric lifetime and fewer chlorine atoms. use of the online ERF, rather than the offline SARF, allows the model physics to account for changes in stratospheric temperature (as well as tropospheric temperature, water vapour and clouds) rather than estimating stratosphere temperature changes using fixed dynamical heating. This online calculation of radiative forcing rather than offline leads to approximately double the indirect GWPs compared to World Meteorological Organization assessments. This formalism can be used with other estimates of ozone ERF, as the indirect GWPs scale linearly with this quantity.

Competing interests: At least one of the (co-)authors is a member of the editorial board of Atmospheric Chemistry and Physics.

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William J. Collins, John S. Daniel, Martyn P. Chipperfield, Martin Cussac, Makoto Deushi, Gregory Faluvegi, Paul Griffiths, Øivind Hodnebrog, Larry W. Horowitz, James Keeble, Douglas Kinnison, Vaishali Naik, Fiona M. O'Connor, Drew Shindell, Simone Tilmes, Kostas Tsigaridis, Zihao Wang, and James Weber

Status: open (until 26 Feb 2026)

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William J. Collins, John S. Daniel, Martyn P. Chipperfield, Martin Cussac, Makoto Deushi, Gregory Faluvegi, Paul Griffiths, Øivind Hodnebrog, Larry W. Horowitz, James Keeble, Douglas Kinnison, Vaishali Naik, Fiona M. O'Connor, Drew Shindell, Simone Tilmes, Kostas Tsigaridis, Zihao Wang, and James Weber
William J. Collins, John S. Daniel, Martyn P. Chipperfield, Martin Cussac, Makoto Deushi, Gregory Faluvegi, Paul Griffiths, Øivind Hodnebrog, Larry W. Horowitz, James Keeble, Douglas Kinnison, Vaishali Naik, Fiona M. O'Connor, Drew Shindell, Simone Tilmes, Kostas Tsigaridis, Zihao Wang, and James Weber
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Short summary
Ozone depleting substances (ODSs) are also greenhouse gases that cause global warming. However, their destruction of ozone contributes a global cooling. We have used results from climate models that include atmospheric chemistry and found that the cooling effect of the ozone depletion diagnosed in the models was larger than that calculated using a standard method. We find that some ODSs have a net cooling effect whereas for others the warming effect is significantly reduced.
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