TY - JOUR
T1 - Multi-model simulations of aerosol and ozone radiative forcing due to anthropogenic emission changes during the period 1990–2015
AU - Myhre, Gunnar
AU - Aas, Wenche
AU - Cherian, Ribu
AU - Collins, William
AU - Faluvegi, Greg
AU - Flanner, Mark
AU - Forster, Piers
AU - Hodnebrog, Øivind
AU - Klimont, Zbigniew
AU - Lund, Marianne T.
AU - Mülmenstädt, Johannes
AU - Lund Myhre, Cathrine
AU - Olivié, Dirk
AU - Prather, Michael
AU - Quaas, Johannes
AU - Samset, Bjørn H.
AU - Schnell, Jordan L.
AU - Schulz, Michael
AU - Shindell, Drew
AU - Skeie, Ragnhild B.
AU - Takemura, Toshihiko
AU - Tsyro, Svetlana
N1 - Funding Information:
This study benefitted from the Norwegian research council projects #229796 (AeroCom-P3) and the European Union Seventh Framework Programme (FP7/2007-2013) project # 282688. Jordan L. Schnell was supported by the National Science Foundation's Graduate Research Fellowship Program (DGE-1321846). We would like to express our thanks those who are involved in the EMEP and IMPROVE monitoring efforts and have contributed through operating sites, performing chemical analysis and by submissions of data. EMEP are funded through national contributions. US Environmental Protection Agency is the primary funding source of IMPROVE, with contracting and research support from the National Park Service. The Air Quality Group at the University of California, Davis is the central analytical laboratory.
Publisher Copyright:
© 2017 Author(s). CC Attribution 3.0 License.
PY - 2017/2/22
Y1 - 2017/2/22
N2 - Over the past few decades, the geographical distribution of emissions of substances that alter the atmospheric energy balance has changed due to economic growth and air pollution regulations. Here, we show the resulting changes to aerosol and ozone abundances and their radiative forcing using recently updated emission data for the period 1990-2015, as simulated by seven global atmospheric composition models. The models broadly reproduce large-scale changes in surface aerosol and ozone based on observations (e.g.-1 to-3%yr-1 in aerosols over the USA and Europe). The global mean radiative forcing due to ozone and aerosol changes over the 1990-2015 period increased by +0.17±0.08Wm-2, with approximately one-third due to ozone. This increase is more strongly positive than that reported in IPCC AR5. The main reasons for the increased positive radiative forcing of aerosols over this period are the substantial reduction of global mean SO2 emissions, which is stronger in the new emission inventory compared to that used in the IPCC analysis, and higher black carbon emissions.
AB - Over the past few decades, the geographical distribution of emissions of substances that alter the atmospheric energy balance has changed due to economic growth and air pollution regulations. Here, we show the resulting changes to aerosol and ozone abundances and their radiative forcing using recently updated emission data for the period 1990-2015, as simulated by seven global atmospheric composition models. The models broadly reproduce large-scale changes in surface aerosol and ozone based on observations (e.g.-1 to-3%yr-1 in aerosols over the USA and Europe). The global mean radiative forcing due to ozone and aerosol changes over the 1990-2015 period increased by +0.17±0.08Wm-2, with approximately one-third due to ozone. This increase is more strongly positive than that reported in IPCC AR5. The main reasons for the increased positive radiative forcing of aerosols over this period are the substantial reduction of global mean SO2 emissions, which is stronger in the new emission inventory compared to that used in the IPCC analysis, and higher black carbon emissions.
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U2 - 10.5194/acp-17-2709-2017
DO - 10.5194/acp-17-2709-2017
M3 - Article
AN - SCOPUS:85013632714
SN - 1680-7316
VL - 17
SP - 2709
EP - 2720
JO - Atmospheric Chemistry and Physics
JF - Atmospheric Chemistry and Physics
IS - 4
ER -