4.7 Article

Effective radiative forcing from emissions of reactive gases and aerosols - a multi-model comparison

Journal

ATMOSPHERIC CHEMISTRY AND PHYSICS
Volume 21, Issue 2, Pages 853-874

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-21-853-2021

Keywords

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Funding

  1. European Union's Horizon 2020 research and innovation programme [641816, 820829]
  2. Research Council of Norway [270061]
  3. Norwegian infrastructure for computational science [NN9560K, NS9560K]
  4. Met Office Hadley Centre Climate Programme - BEIS
  5. Defra [GA01101]
  6. NERC-IIASA Collaborative Research Fellowship [NE/T009381/1]
  7. New Zealand government's Strategic Science Investment Fund (SSIF) through the NIWA pro-gramme CACV
  8. Japan Society for the Promotion of Science [JP18H03363, JP18H05292, JP20K04070]
  9. Environment Research and Technology Development Fund of the Environmental Restoration and Conservation Agency of Japan [JPMEERF20172003, JPMEERF20202003, JPMEERF20205001]
  10. Arctic Challenge for Sustainability II (ArCS II) programme [JPMXD1420318865]
  11. Ministry of the Environment, Japan
  12. supercomputer system of the National Institute for Environmental Studies, Japan
  13. JSPS KAKENHI [JP19H05669]
  14. Norwegian Research Council project KEYCLIM [295046]
  15. National Science Foundation
  16. National Center for Atmospheric Research - NSF [1852977]
  17. NERC [ncas10014] Funding Source: UKRI

Ask authors/readers for more resources

This paper quantifies the pre-industrial to present-day effective radiative forcing of anthropogenic emissions using CMIP6 models. The results show significant impacts from emissions of SO2, organic carbon, and black carbon, while greenhouse gases like methane and nitrous oxide have smaller effects. The differences in ERFs between models reflect variations in aerosol and chemistry schemes, especially in capturing methane-induced forcing.
This paper quantifies the pre-industrial (1850) to present-day (2014) effective radiative forcing (ERF) of anthropogenic emissions of NOX, volatile organic compounds (VOCs; including CO), SO2, NH3, black carbon, organic carbon, and concentrations of methane, N2O and ozone-depleting halocarbons, using CMIP6 models. Concentration and emission changes of reactive species can cause multiple changes in the composition of radiatively active species: tropospheric ozone, stratospheric ozone, stratospheric water vapour, secondary inorganic and organic aerosol, and methane. Where possible we break down the ERFs from each emitted species into the contributions from the composition changes. The ERFs are calculated for each of the models that participated in the AerChemMIP experiments as part of the CMIP6 project, where the relevant model output was available. The 1850 to 2014 multi-model mean ERFs (+/- standard deviations) are -1.03 +/- 0.37 W m(-2) for SO2 emissions, -0.25 +/- 0.09 W m(-2) for organic carbon (OC), 0.15 +/- 0.17 W m(-2) for black carbon (BC) and -0.07 +/- 0.01 W m(-2) for NH3. For the combined aerosols (in the piClim-aer experiment) it is -1.01 +/- 0.25 W m(-2). The multi-model means for the reactive well-mixed greenhouse gases (including any effects on ozone and aerosol chemistry) are 0.67 +/- 0.17 W m(-2) for methane (CH4), 0.26 +/- 0.07 W m(-2) for nitrous oxide (N2O) and 0.12 +/- 0.2 W m(-2) for ozone-depleting halocarbons (HC). Emissions of the ozone precursors nitrogen oxides (NOx) volatile organic compounds and both together (O-3) lead to ERFs of 0.14 +/- 0.13, 0.09 +/- 0.14 and 0.20 +/- 0.07 W m(-2) respectively. The differences in ERFs calculated for the different models reflect differences in the complexity of their aerosol and chemistry schemes, especially in the case of methane where tropospheric chemistry captures increased forcing from ozone production.

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