Articles | Volume 26, issue 21
https://doi.org/10.5194/acp-26-15757-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-26-15757-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Correct use of radiative efficiencies in calculating global warming potentials and other emission metrics
William J. Collins
CORRESPONDING AUTHOR
Department of Meteorology, University of Reading, Reading, RG6 6ET, UK
Øivind Hodnebrog
CICERO Center for International Climate Research, Oslo, Norway
Keith P. Shine
Department of Meteorology, University of Reading, Reading, RG6 6ET, UK
James B. Burkholder
Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration (NOAA), Boulder, Colorado, USA
Related authors
Stephanie Fiedler, Fiona M. O'Connor, Duncan Watson-Parris, Robert J. Allen, William J. Collins, Paul T. Griffiths, Matthew Kasoar, Jarmo Kikstra, Jasper F. Kok, Lee T. Murray, Fabien Paulot, Maria Sand, Steven T. Turnock, James Weber, Laura J. Wilcox, and Vaishali Naik
Geosci. Model Dev., 19, 3477–3508, https://doi.org/10.5194/gmd-19-3477-2026, https://doi.org/10.5194/gmd-19-3477-2026, 2026
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The Aerosol and Chemistry Model Intercomparison Project phase two (AerChemMIP2) allows the community to compare results from contemporary Earth system models. AerChemMIP2 is asking modelling centres to perform experiments following the same protocol. It includes experiments for enabling new science and for tracking progress. Model output will be used for addressing research and policy questions about anthropogenic and natural drivers of climate change, and the impacts on air quality.
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
EGUsphere, https://doi.org/10.5194/egusphere-2025-6033, https://doi.org/10.5194/egusphere-2025-6033, 2026
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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.
William J. Collins, Fiona M. O'Connor, Rachael E. Byrom, Øivind Hodnebrog, Patrick Jöckel, Mariano Mertens, Gunnar Myhre, Matthias Nützel, Dirk Olivié, Ragnhild Bieltvedt Skeie, Laura Stecher, Larry W. Horowitz, Vaishali Naik, Gregory Faluvegi, Ulas Im, Lee T. Murray, Drew Shindell, Kostas Tsigaridis, Nathan Luke Abraham, and James Keeble
Atmos. Chem. Phys., 25, 9031–9060, https://doi.org/10.5194/acp-25-9031-2025, https://doi.org/10.5194/acp-25-9031-2025, 2025
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We used 7 climate models that include atmospheric chemistry and find that in a scenario with weak controls on air quality, the warming effects (over 2015 to 2050) of decreases in ozone-depleting substances and increases in air quality pollutants are approximately equal and would make ozone the second highest contributor to warming over this period. We find that for stratospheric ozone recovery, the standard measure of climate effects underestimates a more comprehensive measure.
Paul T. Griffiths, Laura J. Wilcox, Robert J. Allen, Vaishali Naik, Fiona M. O'Connor, Michael Prather, Alex Archibald, Florence Brown, Makoto Deushi, William Collins, Stephanie Fiedler, Naga Oshima, Lee T. Murray, Bjørn H. Samset, Chris Smith, Steven Turnock, Duncan Watson-Parris, and Paul J. Young
Atmos. Chem. Phys., 25, 8289–8328, https://doi.org/10.5194/acp-25-8289-2025, https://doi.org/10.5194/acp-25-8289-2025, 2025
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The Aerosol Chemistry Model Intercomparison Project (AerChemMIP) aimed to quantify the climate and air quality impacts of aerosols and chemically reactive gases. We review its contribution to AR6 (Sixth Assessment Report of the Intergovernmental Panel on Climate Change) and the wider understanding of the role of these species in climate and climate change. We identify challenges and provide recommendations to improve the utility and uptake of climate model data, detailed summary tables of CMIP6 models, experiments, and emergent diagnostics.
Stephanie Fiedler, Vaishali Naik, Fiona M. O'Connor, Christopher J. Smith, Paul Griffiths, Ryan J. Kramer, Toshihiko Takemura, Robert J. Allen, Ulas Im, Matthew Kasoar, Angshuman Modak, Steven Turnock, Apostolos Voulgarakis, Duncan Watson-Parris, Daniel M. Westervelt, Laura J. Wilcox, Alcide Zhao, William J. Collins, Michael Schulz, Gunnar Myhre, and Piers M. Forster
Geosci. Model Dev., 17, 2387–2417, https://doi.org/10.5194/gmd-17-2387-2024, https://doi.org/10.5194/gmd-17-2387-2024, 2024
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Climate scientists want to better understand modern climate change. Thus, climate model experiments are performed and compared. The results of climate model experiments differ, as assessed in the latest Intergovernmental Panel on Climate Change (IPCC) assessment report. This article gives insights into the challenges and outlines opportunities for further improving the understanding of climate change. It is based on views of a group of experts in atmospheric composition–climate interactions.
David S. Stevenson, Richard G. Derwent, Oliver Wild, and William J. Collins
Atmos. Chem. Phys., 22, 14243–14252, https://doi.org/10.5194/acp-22-14243-2022, https://doi.org/10.5194/acp-22-14243-2022, 2022
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Atmospheric methane’s growth rate rose by 50 % in 2020 relative to 2019. Lower nitrogen oxide (NOx) emissions tend to increase methane’s atmospheric residence time; lower carbon monoxide (CO) and non-methane volatile organic compound (NMVOC) emissions decrease its lifetime. Combining model sensitivities with emission changes, we find that COVID-19 lockdown emission reductions can explain over half the observed increases in methane in 2020.
Daniela Alvarado-Jiménez, Nicola Tasinato, Roberto Buizza, and Keith P. Shine
Atmos. Chem. Phys., 26, 13069–13082, https://doi.org/10.5194/acp-26-13069-2026, https://doi.org/10.5194/acp-26-13069-2026, 2026
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Halocarbon gases (used e.g. in air conditioning) contribute to climate change. Their inclusion in international legislation needs emission metrics that characterise their climate importance; this requires good knowledge of how well they absorb infrared (IR) radiation. Little previous work has quantified absorption at long IR wavelengths. We report new calculations, previously validated against measurements, that improve understanding for 30 gases and allow refined estimates of emission metrics.
Ben Adam, Rayne Holland, Daniel Van Hoomissen, James B. Burkholder, M. Anwar H. Khan, Paul Griffiths, Jens Mühle, Dudley Shallcross, and Matt Rigby
Atmos. Chem. Phys., 26, 10979–10996, https://doi.org/10.5194/acp-26-10979-2026, https://doi.org/10.5194/acp-26-10979-2026, 2026
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Some man-made gases emitted into the atmosphere can break down to form a powerful greenhouse gas called HFC-23 (hydrofluorocarbons). In this study, we use a full three-dimensional model of the atmosphere and its chemistry to improve on previous work and determine how much HFC-23 is produced from this route. Our model estimates HFC-23 production ten times lower than previously suggested, confirming that this source is a very small contributor to the total amount of HFC-23 in the atmosphere.
Srinath Krishnan, Ragnhild Bieltvedt Skeie, Øivind Hodnebrog, Gunnar Myhre, Maria Sand, Marit Sandstad, Hannah Bryant, Didier A. Hauglustaine, Fabien Paulot, Michael Prather, and David Stevenson
Atmos. Chem. Phys., 26, 9509–9539, https://doi.org/10.5194/acp-26-9509-2026, https://doi.org/10.5194/acp-26-9509-2026, 2026
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Hydrogen (H2) is an indirect greenhouse gas that can affect climate through chemical reactions in the atmosphere. To better understand this impact, it is important to constrain the sources and sinks of hydrogen. Using a suite of three-dimensional and one-dimensional models, we find that atmospheric production of hydrogen is 37–60 Tg/yr and that the geological source of H2 is much smaller than suggested. More field and isotopic measurements are needed to improve these estimates.
Stephanie Fiedler, Fiona M. O'Connor, Duncan Watson-Parris, Robert J. Allen, William J. Collins, Paul T. Griffiths, Matthew Kasoar, Jarmo Kikstra, Jasper F. Kok, Lee T. Murray, Fabien Paulot, Maria Sand, Steven T. Turnock, James Weber, Laura J. Wilcox, and Vaishali Naik
Geosci. Model Dev., 19, 3477–3508, https://doi.org/10.5194/gmd-19-3477-2026, https://doi.org/10.5194/gmd-19-3477-2026, 2026
Short summary
Short summary
The Aerosol and Chemistry Model Intercomparison Project phase two (AerChemMIP2) allows the community to compare results from contemporary Earth system models. AerChemMIP2 is asking modelling centres to perform experiments following the same protocol. It includes experiments for enabling new science and for tracking progress. Model output will be used for addressing research and policy questions about anthropogenic and natural drivers of climate change, and the impacts on air quality.
Gunnar Myhre, Øivind Hodnebrog, Srinath Krishnan, Maria Sand, Marit Sandstad, Ragnhild B. Skeie, Lieven Clarisse, Bruno Franco, Dylan B. Millet, Kelley C. Wells, Alexander Archibald, Hannah N. Bryant, Alex T. Chaudhri, David S. Stevenson, Didier Hauglustaine, Michael Prather, J. Christopher Kaiser, Dirk J. L. Olivie, Michael Schulz, Oliver Wild, Ye Wang, Thérèse Salameh, Jason E. Williams, Philippe Le Sager, Fabien Paulot, Kostas Tsigaridis, and Haley E. Plaas
Geosci. Model Dev., 19, 2577–2591, https://doi.org/10.5194/gmd-19-2577-2026, https://doi.org/10.5194/gmd-19-2577-2026, 2026
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Volatile organic compounds (VOCs) affect air quality and climate, but their behavior in the atmosphere is still uncertain. We launched a global research effort to compare how different models represent these compounds and to improve their accuracy. By analyzing model results alongside observations and satellite data, we aim to better understand the atmospheric composition of these compounds.
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
EGUsphere, https://doi.org/10.5194/egusphere-2025-6033, https://doi.org/10.5194/egusphere-2025-6033, 2026
Short summary
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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.
Iris Mužić, Øivind Hodnebrog, Yeliz A. Yilmaz, Terje K. Berntsen, Jana Sillmann, David M. Lawrence, and Paul A. Dirmeyer
Adv. Stat. Clim. Meteorol. Oceanogr., 11, 273–292, https://doi.org/10.5194/ascmo-11-273-2025, https://doi.org/10.5194/ascmo-11-273-2025, 2025
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This study investigates soil moisture–temperature coupling during the extreme warm conditions in May–August 2018 in southern and central Sweden using the merged GLEAM-E-OBS dataset and four simulations from the Weather Research and Forecasting model coupled with the Community Terrestrial Systems Model (WRF-CTSM). Based on changes in surface soil moisture, evaporative fraction, and daily maximum 2 m temperature, on average across the region and five datasets, the coupling lasted for 22 d.
Gabriella Everett, Øivind Hodnebrog, Madhoolika Agrawal, Durgesh Singh Yadav, Connie O'Neill, Chubamenla Jamir, Jo Cook, Pritha Pande, Sam Bland, and Lisa Emberson
Biogeosciences, 22, 4203–4219, https://doi.org/10.5194/bg-22-4203-2025, https://doi.org/10.5194/bg-22-4203-2025, 2025
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Ground-level ozone (O3), heat, and water stress (WS) reduce wheat yields, threatening food security in India. O3, heat, and WS interact as stressed plants close stomata, limiting O3 entry and damage. This study models O3 uptake under rainfed (WS) and irrigated conditions for current and future climates. Results show little O3-related yield loss under WS but higher losses with irrigation. Both climate scenarios increase O3-related losses, highlighting risks to India’s wheat productivity.
William J. Collins, Fiona M. O'Connor, Rachael E. Byrom, Øivind Hodnebrog, Patrick Jöckel, Mariano Mertens, Gunnar Myhre, Matthias Nützel, Dirk Olivié, Ragnhild Bieltvedt Skeie, Laura Stecher, Larry W. Horowitz, Vaishali Naik, Gregory Faluvegi, Ulas Im, Lee T. Murray, Drew Shindell, Kostas Tsigaridis, Nathan Luke Abraham, and James Keeble
Atmos. Chem. Phys., 25, 9031–9060, https://doi.org/10.5194/acp-25-9031-2025, https://doi.org/10.5194/acp-25-9031-2025, 2025
Short summary
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We used 7 climate models that include atmospheric chemistry and find that in a scenario with weak controls on air quality, the warming effects (over 2015 to 2050) of decreases in ozone-depleting substances and increases in air quality pollutants are approximately equal and would make ozone the second highest contributor to warming over this period. We find that for stratospheric ozone recovery, the standard measure of climate effects underestimates a more comprehensive measure.
Paul T. Griffiths, Laura J. Wilcox, Robert J. Allen, Vaishali Naik, Fiona M. O'Connor, Michael Prather, Alex Archibald, Florence Brown, Makoto Deushi, William Collins, Stephanie Fiedler, Naga Oshima, Lee T. Murray, Bjørn H. Samset, Chris Smith, Steven Turnock, Duncan Watson-Parris, and Paul J. Young
Atmos. Chem. Phys., 25, 8289–8328, https://doi.org/10.5194/acp-25-8289-2025, https://doi.org/10.5194/acp-25-8289-2025, 2025
Short summary
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The Aerosol Chemistry Model Intercomparison Project (AerChemMIP) aimed to quantify the climate and air quality impacts of aerosols and chemically reactive gases. We review its contribution to AR6 (Sixth Assessment Report of the Intergovernmental Panel on Climate Change) and the wider understanding of the role of these species in climate and climate change. We identify challenges and provide recommendations to improve the utility and uptake of climate model data, detailed summary tables of CMIP6 models, experiments, and emergent diagnostics.
Rachael E. Byrom, Gunnar Myhre, Øivind Hodnebrog, Dirk Olivié, and Michael Schulz
Atmos. Chem. Phys., 25, 5683–5693, https://doi.org/10.5194/acp-25-5683-2025, https://doi.org/10.5194/acp-25-5683-2025, 2025
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Addressing the cause of model spread in CO2 effective radiative forcing (ERF) is important for reducing uncertainty in climate change. We investigate stratospheric O3 as a driver of this spread by altering its concentration by 50 % and analysing the impact on CO2 forcing. Our experiments show a significant effect on stratospheric temperature that impacts instantaneous radiative forcing, primarily due to the influence on longwave emission. However, the impact on ERF is minimal.
Zachary Finewax, Aparajeo Chattopadhyay, J. Andrew Neuman, James M. Roberts, and James B. Burkholder
Atmos. Meas. Tech., 17, 6865–6873, https://doi.org/10.5194/amt-17-6865-2024, https://doi.org/10.5194/amt-17-6865-2024, 2024
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This work provides a comprehensive sensitivity calibration of a chemical ionization instrument commonly used in field measurements for the measurement of the toxic isomers methyl isocyanate and hydroxyacetonitrile that are found in the atmosphere. The results from this work have demonstrated that the hydroyacetonitrile isomer was observed in previous field studies rather than the stated identification of methyl isocyanate.
Ragnhild Bieltvedt Skeie, Rachael Byrom, Øivind Hodnebrog, Caroline Jouan, and Gunnar Myhre
Atmos. Chem. Phys., 24, 13361–13370, https://doi.org/10.5194/acp-24-13361-2024, https://doi.org/10.5194/acp-24-13361-2024, 2024
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In 2020, new regulations by the International Maritime Organization regarding sulfur emissions came into force, reducing emissions of SO2 from the shipping sector by approximately 80 %. In this study, we use multiple models to calculate how much the Earth energy balance changed due to the emission reduction or the so-called effective radiative forcing. The calculated effective radiative forcing is weak, comparable to the effect of the increase in CO2 over the last 2 to 3 years.
Audran Borella, Olivier Boucher, Keith P. Shine, Marc Stettler, Katsumasa Tanaka, Roger Teoh, and Nicolas Bellouin
Atmos. Chem. Phys., 24, 9401–9417, https://doi.org/10.5194/acp-24-9401-2024, https://doi.org/10.5194/acp-24-9401-2024, 2024
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This work studies how to compare the climate impact of the CO2 emitted and contrails formed by a flight. This is applied to contrail avoidance strategies that would decrease climate impact of flights by changing the trajectory of aircraft to avoid persistent contrail formation, at the risk of increasing CO2 emissions. We find that different comparison methods lead to different quantification of the total climate impact of a flight but lead to similar decisions of whether to reroute an aircraft.
Stephanie Fiedler, Vaishali Naik, Fiona M. O'Connor, Christopher J. Smith, Paul Griffiths, Ryan J. Kramer, Toshihiko Takemura, Robert J. Allen, Ulas Im, Matthew Kasoar, Angshuman Modak, Steven Turnock, Apostolos Voulgarakis, Duncan Watson-Parris, Daniel M. Westervelt, Laura J. Wilcox, Alcide Zhao, William J. Collins, Michael Schulz, Gunnar Myhre, and Piers M. Forster
Geosci. Model Dev., 17, 2387–2417, https://doi.org/10.5194/gmd-17-2387-2024, https://doi.org/10.5194/gmd-17-2387-2024, 2024
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Climate scientists want to better understand modern climate change. Thus, climate model experiments are performed and compared. The results of climate model experiments differ, as assessed in the latest Intergovernmental Panel on Climate Change (IPCC) assessment report. This article gives insights into the challenges and outlines opportunities for further improving the understanding of climate change. It is based on views of a group of experts in atmospheric composition–climate interactions.
Ryan S. Williams, Michaela I. Hegglin, Patrick Jöckel, Hella Garny, and Keith P. Shine
Atmos. Chem. Phys., 24, 1389–1413, https://doi.org/10.5194/acp-24-1389-2024, https://doi.org/10.5194/acp-24-1389-2024, 2024
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During winter, a brief but abrupt reversal of the mean stratospheric westerly flow (~30 km high) around the Arctic occurs ~6 times a decade. Using a chemistry–climate model, about half of these events are shown to induce large anomalies in Arctic ozone (>25 %) and water vapour (>±25 %) around ~8–12 km altitude for up to 2–3 months, important for weather forecasting. We also calculate a doubling to trebling of the risk in breaches of mid-latitude surface air quality (ozone) standards (~60 ppbv).
Nicola J. Warwick, Alex T. Archibald, Paul T. Griffiths, James Keeble, Fiona M. O'Connor, John A. Pyle, and Keith P. Shine
Atmos. Chem. Phys., 23, 13451–13467, https://doi.org/10.5194/acp-23-13451-2023, https://doi.org/10.5194/acp-23-13451-2023, 2023
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A chemistry–climate model has been used to explore the atmospheric response to changes in emissions of hydrogen and other species associated with a shift from fossil fuel to hydrogen use. Leakage of hydrogen results in indirect global warming, offsetting greenhouse gas emission reductions from reduced fossil fuel use. To maximise the benefit of hydrogen as an energy source, hydrogen leakage and emissions of methane, carbon monoxide and nitrogen oxides should be minimised.
Feijia Yin, Volker Grewe, Federica Castino, Pratik Rao, Sigrun Matthes, Katrin Dahlmann, Simone Dietmüller, Christine Frömming, Hiroshi Yamashita, Patrick Peter, Emma Klingaman, Keith P. Shine, Benjamin Lührs, and Florian Linke
Geosci. Model Dev., 16, 3313–3334, https://doi.org/10.5194/gmd-16-3313-2023, https://doi.org/10.5194/gmd-16-3313-2023, 2023
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This paper describes a newly developed submodel ACCF V1.0 based on the MESSy 2.53.0 infrastructure. The ACCF V1.0 is based on the prototype algorithmic climate change functions (aCCFs) v1.0 to enable climate-optimized flight trajectories. One highlight of this paper is that we describe a consistent full set of aCCFs formulas with respect to fuel scenario and metrics. We demonstrate the usage of the ACCF submodel using AirTraf V2.0 to optimize trajectories for cost and climate impact.
David S. Stevenson, Richard G. Derwent, Oliver Wild, and William J. Collins
Atmos. Chem. Phys., 22, 14243–14252, https://doi.org/10.5194/acp-22-14243-2022, https://doi.org/10.5194/acp-22-14243-2022, 2022
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Atmospheric methane’s growth rate rose by 50 % in 2020 relative to 2019. Lower nitrogen oxide (NOx) emissions tend to increase methane’s atmospheric residence time; lower carbon monoxide (CO) and non-methane volatile organic compound (NMVOC) emissions decrease its lifetime. Combining model sensitivities with emission changes, we find that COVID-19 lockdown emission reductions can explain over half the observed increases in methane in 2020.
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Editorial statement
Global Warming Potentials (GWPs) convert a gas's radiative efficiency (RE) into a mass-based quantity (W m⁻² kg⁻¹) using the molecular weight and total atmospheric mass. REs are almost universally reported and used as radiative forcing per change in surface mole fraction, because that's what's measured and what radiative transfer models typically vary. For gases with non-uniform vertical profiles — those destroyed in the stratosphere (like CFCs, N₂O) or with short tropospheric lifetimes (many HFCs, HCFCs) — the surface mole fraction is higher than the atmosphere-wide mean, so plugging the surface-based RE directly into the mass-conversion formula systematically underestimates the actual mass-based radiative efficiency, and therefore underestimates the GWP. In this letter, the authors derive a correction factor (the ratio of the change in surface mole fraction to the change in mean atmospheric mole fraction) and provide empirical fits so this ratio can be estimated for any gas even without access to the original radiative transfer model output, leading to an upward revision of GWP values. The work has real potential consequences for regulatory thresholds and reported emissions-weighted climate impacts.
Global Warming Potentials (GWPs) convert a gas's radiative efficiency (RE) into a mass-based...
Short summary
The global warming potential (GWP) is a commonly used metric for relating the climate impact of emissions of a gas relative to that for carbon dioxide. We show that previous calculations have systematically underestimated these values by applying calculations of radiative forcing efficiency appropriate to changes in surface mole fractions rather than changes in the mass-weighted mean mole fraction in the atmosphere.
The global warming potential (GWP) is a commonly used metric for relating the climate impact of...
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