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description Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 Norway, France, United Kingdom, France, Norway, France, GermanyPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYDavid A. Plummer; Larry W. Horowitz; Oliver Wild; Ruth M. Doherty; Drew Shindell; Dan Bergmann; Vaishali Naik; Alexander T. Archibald; Sarah A. Strode; Sarah A. Strode; Gregory Faluvegi; Sophie Szopa; Philip Cameron-Smith; Irene Cionni; Béatrice Josse; Kengo Sudo; Apostolos Voulgarakis; Veronika Eyring; S. T. Rumbold; Ian A. MacKenzie; Simone Tilmes; Y. H. Lee; Ragnhild Bieltvedt Skeie; T. Nagashima; Kevin W. Bowman; Paul Young; Paul Young; Paul Young; William J. Collins; William J. Collins; Mattia Righi; Guang Zeng; Jean-Francois Lamarque; S. B. Dalsøren; David Stevenson;Abstract. Present day tropospheric ozone and its changes between 1850 and 2100 are considered, analysing 15 global models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The multi-model mean compares well against present day observations. The seasonal cycle correlates well, except for some locations in the tropical upper troposphere. Most (75%) of the models are encompassed with a range of global mean tropospheric ozone column estimates from satellite data, although there is a suggestion of a high bias in the Northern Hemisphere and a low bias in the Southern Hemisphere. Compared to the present day multi-model mean tropospheric ozone burden of 337 Tg, the multi-model mean burden for 1850 time slice is ~ 30% lower. Future changes were modelled using emissions and climate projections from four Representative Concentration Pathways (RCPs). Compared to 2000, the relative changes for the tropospheric ozone burden in 2030 (2100) for the different RCPs are: −5% (−22%) for RCP2.6, 3% (−8%) for RCP4.5, 0% (−9%) for RCP6.0, and 5% (15%) for RCP8.5. Model agreement on the magnitude of the change is greatest for larger changes. Reductions in precursor emissions are common across the RCPs and drive ozone decreases in all but RCP8.5, where doubled methane and a larger stratospheric influx increase ozone. Models with high ozone abundances for the present day also have high ozone levels for the other time slices, but there are no models consistently predicting large or small changes. Spatial patterns of ozone changes are well correlated across most models, but are notably different for models without time evolving stratospheric ozone concentrations. A unified approach to ozone budget specifications is recommended to help future studies attribute ozone changes and inter-model differences more clearly.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu514 citations 514 popularity Top 0.1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 Norway, France, United Kingdom, France, Norway, France, GermanyPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYDavid A. Plummer; Larry W. Horowitz; Oliver Wild; Ruth M. Doherty; Drew Shindell; Dan Bergmann; Vaishali Naik; Alexander T. Archibald; Sarah A. Strode; Sarah A. Strode; Gregory Faluvegi; Sophie Szopa; Philip Cameron-Smith; Irene Cionni; Béatrice Josse; Kengo Sudo; Apostolos Voulgarakis; Veronika Eyring; S. T. Rumbold; Ian A. MacKenzie; Simone Tilmes; Y. H. Lee; Ragnhild Bieltvedt Skeie; T. Nagashima; Kevin W. Bowman; Paul Young; Paul Young; Paul Young; William J. Collins; William J. Collins; Mattia Righi; Guang Zeng; Jean-Francois Lamarque; S. B. Dalsøren; David Stevenson;Abstract. Present day tropospheric ozone and its changes between 1850 and 2100 are considered, analysing 15 global models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The multi-model mean compares well against present day observations. The seasonal cycle correlates well, except for some locations in the tropical upper troposphere. Most (75%) of the models are encompassed with a range of global mean tropospheric ozone column estimates from satellite data, although there is a suggestion of a high bias in the Northern Hemisphere and a low bias in the Southern Hemisphere. Compared to the present day multi-model mean tropospheric ozone burden of 337 Tg, the multi-model mean burden for 1850 time slice is ~ 30% lower. Future changes were modelled using emissions and climate projections from four Representative Concentration Pathways (RCPs). Compared to 2000, the relative changes for the tropospheric ozone burden in 2030 (2100) for the different RCPs are: −5% (−22%) for RCP2.6, 3% (−8%) for RCP4.5, 0% (−9%) for RCP6.0, and 5% (15%) for RCP8.5. Model agreement on the magnitude of the change is greatest for larger changes. Reductions in precursor emissions are common across the RCPs and drive ozone decreases in all but RCP8.5, where doubled methane and a larger stratospheric influx increase ozone. Models with high ozone abundances for the present day also have high ozone levels for the other time slices, but there are no models consistently predicting large or small changes. Spatial patterns of ozone changes are well correlated across most models, but are notably different for models without time evolving stratospheric ozone concentrations. A unified approach to ozone budget specifications is recommended to help future studies attribute ozone changes and inter-model differences more clearly.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu514 citations 514 popularity Top 0.1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2013 France, United Kingdom, France, France, Norway, Germany, NorwayPublisher:Copernicus GmbH Kengo Sudo; Gunnar Myhre; Ragnhild Bieltvedt Skeie; Tatsuya Nagashima; Terje Koren Berntsen; T. P. C. van Noije; Larry W. Horowitz; Sophie Szopa; Drew Shindell; Dan Bergmann; Vaishali Naik; Andrew Conley; Alexander T. Archibald; S. T. Rumbold; Y. H. Lee; Irene Cionni; Jean-Francois Lamarque; Sarah A. Strode; Sarah A. Strode; Ruth M. Doherty; David A. Plummer; Gerd A. Folberth; S. B. Dalsøren; Oliver Wild; Philip Cameron-Smith; Ian A. MacKenzie; Veronika Eyring; Béatrice Josse; A. Strunk; Kevin W. Bowman; Apostolos Voulgarakis; Mattia Righi; William J. Collins; William J. Collins; Paul Young; Paul Young; Paul Young; Guang Zeng; David Stevenson;Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2013 France, United Kingdom, France, France, Norway, Germany, NorwayPublisher:Copernicus GmbH Kengo Sudo; Gunnar Myhre; Ragnhild Bieltvedt Skeie; Tatsuya Nagashima; Terje Koren Berntsen; T. P. C. van Noije; Larry W. Horowitz; Sophie Szopa; Drew Shindell; Dan Bergmann; Vaishali Naik; Andrew Conley; Alexander T. Archibald; S. T. Rumbold; Y. H. Lee; Irene Cionni; Jean-Francois Lamarque; Sarah A. Strode; Sarah A. Strode; Ruth M. Doherty; David A. Plummer; Gerd A. Folberth; S. B. Dalsøren; Oliver Wild; Philip Cameron-Smith; Ian A. MacKenzie; Veronika Eyring; Béatrice Josse; A. Strunk; Kevin W. Bowman; Apostolos Voulgarakis; Mattia Righi; William J. Collins; William J. Collins; Paul Young; Paul Young; Paul Young; Guang Zeng; David Stevenson;Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United States, France, Germany, United KingdomPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYGregory Faluvegi; Apostolos Voulgarakis; Apostolos Voulgarakis; Sophie Szopa; Béatrice Josse; Larry W. Horowitz; Ian A. MacKenzie; Robert D. Field; Robert D. Field; Oliver Wild; Drew Shindell; Dan Bergmann; Vaishali Naik; Gerd A. Folberth; S. B. Dalsøren; Tatsuya Nagashima; Guang Zeng; Michael J. Prather; S. T. Rumbold; Philip Cameron-Smith; David A. Plummer; Irene Cionni; David Stevenson; Sarah A. Strode; William J. Collins; William J. Collins; Ruth M. Doherty; Paul Young; Paul Young; Paul Young; Jean-Francois Lamarque; Veronika Eyring; Mattia Righi; Kengo Sudo;Abstract. Results from simulations performed for the Atmospheric Chemistry and Climate Modeling Intercomparison Project (ACCMIP) are analysed to examine how OH and methane lifetime may change from present-day to the future, under different climate and emissions scenarios. Present-day (2000) mean tropospheric chemical lifetime derived from the ACCMIP multi-model mean is 9.8 ± 1.6 yr, lower than a recent observationally-based estimate, but with a similar range to previous multi-model estimates. Future model projections are based on the four Representative Concentration Pathways (RCPs), and the results also exhibit a~large range. Decreases in global methane lifetime of 4.5 ± 9.1% are simulated for the scenario with lowest radiative forcing by 2100 (RCP 2.6), while increases of 8.5 ± 10.4% are simulated for the scenario with highest radiative forcing (RCP 8.5). In this scenario, the key driver of the evolution of OH and methane lifetime is methane itself, since its concentration more than doubles by 2100, and it consumes much of the OH that exists in the troposphere. Stratospheric ozone recovery, which drives tropospheric OH decreases through photolysis modifications, also plays a~partial role. In the other scenarios, where methane changes are less drastic, the interplay between various competing drivers leads to smaller and more diverse OH and methane lifetime responses, which are difficult to attribute. For all scenarios, regional OH changes are even more variable, with the most robust feature being the large decreases over the remote oceans in RCP 8.5. Through a~regression analysis, we suggest that differences in emissions of non-methane volatile organic compounds and in the simulation of photolysis rates may be the main factors causing the differences in simulated present-day OH and methane lifetime. Diversity in predicted changes between present-day and future was found to be associated more strongly with differences in modelled climate changes, specifically global temperature and humidity. Finally, through perturbation experiments we calculated an OH feedback factor (F) of 1.29 from present-day conditions (1.65 from 2100 RCP 8.5 conditions) and a~climate feedback on methane lifetime of 0.33 ± 0.13 yr K−1, on average.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu241 citations 241 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United States, France, Germany, United KingdomPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYGregory Faluvegi; Apostolos Voulgarakis; Apostolos Voulgarakis; Sophie Szopa; Béatrice Josse; Larry W. Horowitz; Ian A. MacKenzie; Robert D. Field; Robert D. Field; Oliver Wild; Drew Shindell; Dan Bergmann; Vaishali Naik; Gerd A. Folberth; S. B. Dalsøren; Tatsuya Nagashima; Guang Zeng; Michael J. Prather; S. T. Rumbold; Philip Cameron-Smith; David A. Plummer; Irene Cionni; David Stevenson; Sarah A. Strode; William J. Collins; William J. Collins; Ruth M. Doherty; Paul Young; Paul Young; Paul Young; Jean-Francois Lamarque; Veronika Eyring; Mattia Righi; Kengo Sudo;Abstract. Results from simulations performed for the Atmospheric Chemistry and Climate Modeling Intercomparison Project (ACCMIP) are analysed to examine how OH and methane lifetime may change from present-day to the future, under different climate and emissions scenarios. Present-day (2000) mean tropospheric chemical lifetime derived from the ACCMIP multi-model mean is 9.8 ± 1.6 yr, lower than a recent observationally-based estimate, but with a similar range to previous multi-model estimates. Future model projections are based on the four Representative Concentration Pathways (RCPs), and the results also exhibit a~large range. Decreases in global methane lifetime of 4.5 ± 9.1% are simulated for the scenario with lowest radiative forcing by 2100 (RCP 2.6), while increases of 8.5 ± 10.4% are simulated for the scenario with highest radiative forcing (RCP 8.5). In this scenario, the key driver of the evolution of OH and methane lifetime is methane itself, since its concentration more than doubles by 2100, and it consumes much of the OH that exists in the troposphere. Stratospheric ozone recovery, which drives tropospheric OH decreases through photolysis modifications, also plays a~partial role. In the other scenarios, where methane changes are less drastic, the interplay between various competing drivers leads to smaller and more diverse OH and methane lifetime responses, which are difficult to attribute. For all scenarios, regional OH changes are even more variable, with the most robust feature being the large decreases over the remote oceans in RCP 8.5. Through a~regression analysis, we suggest that differences in emissions of non-methane volatile organic compounds and in the simulation of photolysis rates may be the main factors causing the differences in simulated present-day OH and methane lifetime. Diversity in predicted changes between present-day and future was found to be associated more strongly with differences in modelled climate changes, specifically global temperature and humidity. Finally, through perturbation experiments we calculated an OH feedback factor (F) of 1.29 from present-day conditions (1.65 from 2100 RCP 8.5 conditions) and a~climate feedback on methane lifetime of 0.33 ± 0.13 yr K−1, on average.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu241 citations 241 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, United States, United States, France, France, United States, United States, Norway, Norway, GermanyPublisher:Copernicus GmbH S. T. Rumbold; Gregory Faluvegi; Ian A. MacKenzie; Michael J. Prather; Y. H. Lee; Sophie Szopa; Larry W. Horowitz; Guang Zeng; Jean-Francois Lamarque; Kengo Sudo; T. P. C. van Noije; Meiyun Lin; Meiyun Lin; David Stevenson; Gerd A. Folberth; Ruth M. Doherty; Ragnhild Bieltvedt Skeie; Sarah A. Strode; Mattia Righi; William J. Collins; William J. Collins; Veronika Eyring; Béatrice Josse; Tatsuya Nagashima; Paul Young; Paul Young; Paul Young; Drew Shindell; Vaishali Naik; Arlene M. Fiore; David A. Plummer; Daniel Bergmann; Philip Cameron-Smith; S. B. Dalsøren; Irene Cionni; Apostolos Voulgarakis;Abstract. We have analysed time-slice simulations from 17 global models, participating in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), to explore changes in present-day (2000) hydroxyl radical (OH) concentration and methane (CH4) lifetime relative to preindustrial times (1850) and to 1980. A comparison of modeled and observation-derived methane and methyl chloroform lifetimes suggests that the present-day global multi-model mean OH concentration is overestimated by 5 to 10% but is within the range of uncertainties. The models consistently simulate higher OH concentrations in the Northern Hemisphere (NH) compared with the Southern Hemisphere (SH) for the present-day (2000; inter-hemispheric ratios of 1.13 to 1.42), in contrast to observation-based approaches which generally indicate higher OH in the SH although uncertainties are large. Evaluation of simulated carbon monoxide (CO) concentrations, the primary sink for OH, against ground-based and satellite observations suggests low biases in the NH that may contribute to the high north–south OH asymmetry in the models. The models vary widely in their regional distribution of present-day OH concentrations (up to 34%). Despite large regional changes, the multi-model global mean (mass-weighted) OH concentration changes little over the past 150 yr, due to concurrent increases in factors that enhance OH (humidity, tropospheric ozone, nitrogen oxide (NOx) emissions, and UV radiation due to decreases in stratospheric ozone), compensated by increases in OH sinks (methane abundance, carbon monoxide and non-methane volatile organic carbon (NMVOC) emissions). The large inter-model diversity in the sign and magnitude of preindustrial to present-day OH changes (ranging from a decrease of 12.7% to an increase of 14.6%) indicate that uncertainty remains in our understanding of the long-term trends in OH and methane lifetime. We show that this diversity is largely explained by the different ratio of the change in global mean tropospheric CO and NOx burdens (ΔCO/ΔNOx, approximately represents changes in OH sinks versus changes in OH sources) in the models, pointing to a need for better constraints on natural precursor emissions and on the chemical mechanisms in the current generation of chemistry-climate models. For the 1980 to 2000 period, we find that climate warming and a slight increase in mean OH (3.5 ± 2.2%) leads to a 4.3 ± 1.9% decrease in the methane lifetime. Analysing sensitivity simulations performed by 10 models, we find that preindustrial to present-day climate change decreased the methane lifetime by about four months, representing a negative feedback on the climate system. Further, we analysed attribution experiments performed by a subset of models relative to 2000 conditions with only one precursor at a time set to 1860 levels. We find that global mean OH increased by 46.4 ± 12.2% in response to preindustrial to present-day anthropogenic NOx emission increases, and decreased by 17.3 ± 2.3%, 7.6 ± 1.5%, and 3.1 ± 3.0% due to methane burden, and anthropogenic CO, and NMVOC emissions increases, respectively.
Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu274 citations 274 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, United States, United States, France, France, United States, United States, Norway, Norway, GermanyPublisher:Copernicus GmbH S. T. Rumbold; Gregory Faluvegi; Ian A. MacKenzie; Michael J. Prather; Y. H. Lee; Sophie Szopa; Larry W. Horowitz; Guang Zeng; Jean-Francois Lamarque; Kengo Sudo; T. P. C. van Noije; Meiyun Lin; Meiyun Lin; David Stevenson; Gerd A. Folberth; Ruth M. Doherty; Ragnhild Bieltvedt Skeie; Sarah A. Strode; Mattia Righi; William J. Collins; William J. Collins; Veronika Eyring; Béatrice Josse; Tatsuya Nagashima; Paul Young; Paul Young; Paul Young; Drew Shindell; Vaishali Naik; Arlene M. Fiore; David A. Plummer; Daniel Bergmann; Philip Cameron-Smith; S. B. Dalsøren; Irene Cionni; Apostolos Voulgarakis;Abstract. We have analysed time-slice simulations from 17 global models, participating in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), to explore changes in present-day (2000) hydroxyl radical (OH) concentration and methane (CH4) lifetime relative to preindustrial times (1850) and to 1980. A comparison of modeled and observation-derived methane and methyl chloroform lifetimes suggests that the present-day global multi-model mean OH concentration is overestimated by 5 to 10% but is within the range of uncertainties. The models consistently simulate higher OH concentrations in the Northern Hemisphere (NH) compared with the Southern Hemisphere (SH) for the present-day (2000; inter-hemispheric ratios of 1.13 to 1.42), in contrast to observation-based approaches which generally indicate higher OH in the SH although uncertainties are large. Evaluation of simulated carbon monoxide (CO) concentrations, the primary sink for OH, against ground-based and satellite observations suggests low biases in the NH that may contribute to the high north–south OH asymmetry in the models. The models vary widely in their regional distribution of present-day OH concentrations (up to 34%). Despite large regional changes, the multi-model global mean (mass-weighted) OH concentration changes little over the past 150 yr, due to concurrent increases in factors that enhance OH (humidity, tropospheric ozone, nitrogen oxide (NOx) emissions, and UV radiation due to decreases in stratospheric ozone), compensated by increases in OH sinks (methane abundance, carbon monoxide and non-methane volatile organic carbon (NMVOC) emissions). The large inter-model diversity in the sign and magnitude of preindustrial to present-day OH changes (ranging from a decrease of 12.7% to an increase of 14.6%) indicate that uncertainty remains in our understanding of the long-term trends in OH and methane lifetime. We show that this diversity is largely explained by the different ratio of the change in global mean tropospheric CO and NOx burdens (ΔCO/ΔNOx, approximately represents changes in OH sinks versus changes in OH sources) in the models, pointing to a need for better constraints on natural precursor emissions and on the chemical mechanisms in the current generation of chemistry-climate models. For the 1980 to 2000 period, we find that climate warming and a slight increase in mean OH (3.5 ± 2.2%) leads to a 4.3 ± 1.9% decrease in the methane lifetime. Analysing sensitivity simulations performed by 10 models, we find that preindustrial to present-day climate change decreased the methane lifetime by about four months, representing a negative feedback on the climate system. Further, we analysed attribution experiments performed by a subset of models relative to 2000 conditions with only one precursor at a time set to 1860 levels. We find that global mean OH increased by 46.4 ± 12.2% in response to preindustrial to present-day anthropogenic NOx emission increases, and decreased by 17.3 ± 2.3%, 7.6 ± 1.5%, and 3.1 ± 3.0% due to methane burden, and anthropogenic CO, and NMVOC emissions increases, respectively.
Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu274 citations 274 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 France, France, France, Germany, United StatesPublisher:Royal Society of Chemistry (RSC) Fiore, Arlene; Naik, Vaishali; Spracklen, Dominick; Steiner, Allison; Unger, Nadine; Prather, Michael; Bergmann, Dan; Cameron-Smith, Philip; Cionni, Irene; Collins, William; Dalsøren, Stig; Eyring, Veronika; Folberth, Gerd; Ginoux, Paul; Horowitz, Larry; Josse, Béatrice; Lamarque, Jean-François; Mackenzie, Ian; Nagashima, Tatsuya; O'Connor, Fiona; Righi, Mattia; Rumbold, Steven; Shindell, Drew; Skeie, Ragnhild; Sudo, Kengo; Szopa, Sophie; Takemura, Toshihiko; Zeng, Guang;pmid: 22868337
Emissions of air pollutants and their precursors determine regional air quality and can alter climate. Climate change can perturb the long-range transport, chemical processing, and local meteorology that influence air pollution. We review the implications of projected changes in methane (CH4), ozone precursors (O3), and aerosols for climate (expressed in terms of the radiative forcing metric or changes in global surface temperature) and hemispheric-to-continental scale air quality. Reducing the O3 precursor CH4 would slow near-term warming by decreasing both CH4 and tropospheric O3. Uncertainty remains as to the net climate forcing from anthropogenic nitrogen oxide (NOx) emissions, which increase tropospheric O3 (warming) but also increase aerosols and decrease CH4 (both cooling). Anthropogenic emissions of carbon monoxide (CO) and non-CH4 volatile organic compounds (NMVOC) warm by increasing both O3 and CH4. Radiative impacts from secondary organic aerosols (SOA) are poorly understood. Black carbon emission controls, by reducing the absorption of sunlight in the atmosphere and on snow and ice, have the potential to slow near-term warming, but uncertainties in coincident emissions of reflective (cooling) aerosols and poorly constrained cloud indirect effects confound robust estimates of net climate impacts. Reducing sulfate and nitrate aerosols would improve air quality and lessen interference with the hydrologic cycle, but lead to warming. A holistic and balanced view is thus needed to assess how air pollution controls influence climate; a first step towards this goal involves estimating net climate impacts from individual emission sectors. Modeling and observational analyses suggest a warming climate degrades air quality (increasing surface O3 and particulate matter) in many populated regions, including during pollution episodes. Prior Intergovernmental Panel on Climate Change (IPCC) scenarios (SRES) allowed unconstrained growth, whereas the Representative Concentration Pathway (RCP) scenarios assume uniformly an aggressive reduction, of air pollutant emissions. New estimates from the current generation of chemistry–climate models with RCP emissions thus project improved air quality over the next century relative to those using the IPCC SRES scenarios. These two sets of projections likely bracket possible futures. We find that uncertainty in emission-driven changes in air quality is generally greater than uncertainty in climate-driven changes. Confidence in air quality projections is limited by the reliability of anthropogenic emission trajectories and the uncertainties in regional climate responses, feedbacks with the terrestrial biosphere, and oxidation pathways affecting O3 and SOA.
Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 415 citations 415 popularity Top 1% influence Top 1% impulse Top 0.1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 France, France, France, Germany, United StatesPublisher:Royal Society of Chemistry (RSC) Fiore, Arlene; Naik, Vaishali; Spracklen, Dominick; Steiner, Allison; Unger, Nadine; Prather, Michael; Bergmann, Dan; Cameron-Smith, Philip; Cionni, Irene; Collins, William; Dalsøren, Stig; Eyring, Veronika; Folberth, Gerd; Ginoux, Paul; Horowitz, Larry; Josse, Béatrice; Lamarque, Jean-François; Mackenzie, Ian; Nagashima, Tatsuya; O'Connor, Fiona; Righi, Mattia; Rumbold, Steven; Shindell, Drew; Skeie, Ragnhild; Sudo, Kengo; Szopa, Sophie; Takemura, Toshihiko; Zeng, Guang;pmid: 22868337
Emissions of air pollutants and their precursors determine regional air quality and can alter climate. Climate change can perturb the long-range transport, chemical processing, and local meteorology that influence air pollution. We review the implications of projected changes in methane (CH4), ozone precursors (O3), and aerosols for climate (expressed in terms of the radiative forcing metric or changes in global surface temperature) and hemispheric-to-continental scale air quality. Reducing the O3 precursor CH4 would slow near-term warming by decreasing both CH4 and tropospheric O3. Uncertainty remains as to the net climate forcing from anthropogenic nitrogen oxide (NOx) emissions, which increase tropospheric O3 (warming) but also increase aerosols and decrease CH4 (both cooling). Anthropogenic emissions of carbon monoxide (CO) and non-CH4 volatile organic compounds (NMVOC) warm by increasing both O3 and CH4. Radiative impacts from secondary organic aerosols (SOA) are poorly understood. Black carbon emission controls, by reducing the absorption of sunlight in the atmosphere and on snow and ice, have the potential to slow near-term warming, but uncertainties in coincident emissions of reflective (cooling) aerosols and poorly constrained cloud indirect effects confound robust estimates of net climate impacts. Reducing sulfate and nitrate aerosols would improve air quality and lessen interference with the hydrologic cycle, but lead to warming. A holistic and balanced view is thus needed to assess how air pollution controls influence climate; a first step towards this goal involves estimating net climate impacts from individual emission sectors. Modeling and observational analyses suggest a warming climate degrades air quality (increasing surface O3 and particulate matter) in many populated regions, including during pollution episodes. Prior Intergovernmental Panel on Climate Change (IPCC) scenarios (SRES) allowed unconstrained growth, whereas the Representative Concentration Pathway (RCP) scenarios assume uniformly an aggressive reduction, of air pollutant emissions. New estimates from the current generation of chemistry–climate models with RCP emissions thus project improved air quality over the next century relative to those using the IPCC SRES scenarios. These two sets of projections likely bracket possible futures. We find that uncertainty in emission-driven changes in air quality is generally greater than uncertainty in climate-driven changes. Confidence in air quality projections is limited by the reliability of anthropogenic emission trajectories and the uncertainties in regional climate responses, feedbacks with the terrestrial biosphere, and oxidation pathways affecting O3 and SOA.
Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 415 citations 415 popularity Top 1% influence Top 1% impulse Top 0.1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, Norway, France, Germany, France, NorwayPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYS. B. Dalsøren; Sarah A. Strode; Sarah A. Strode; Larry W. Horowitz; Ruth M. Doherty; David A. Plummer; Apostolos Voulgarakis; David Stevenson; Michael Schulz; Veronika Eyring; Gregory Faluvegi; Sophie Szopa; Y. H. Lee; Steven J. Ghan; Béatrice Josse; Ian A. MacKenzie; Philip Cameron-Smith; Paul Young; Paul Young; Paul Young; Ragnhild Bieltvedt Skeie; Drew Shindell; Dan Bergmann; Vaishali Naik; William J. Collins; William J. Collins; Guang Zeng; T. Nagashima; Gerd A. Folberth; S. T. Rumbold; Kengo Sudo; Irene Cionni; Mattia Righi; Jean-Francois Lamarque;Abstract. The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) consists of a series of time slice experiments targeting the long-term changes in atmospheric composition between 1850 and 2100, with the goal of documenting composition changes and the associated radiative forcing. In this overview paper, we introduce the ACCMIP activity, the various simulations performed (with a requested set of 14) and the associated model output. The 16 ACCMIP models have a wide range of horizontal and vertical resolutions, vertical extent, chemistry schemes and interaction with radiation and clouds. While anthropogenic and biomass burning emissions were specified for all time slices in the ACCMIP protocol, it is found that the natural emissions are responsible for a significant range across models, mostly in the case of ozone precursors. The analysis of selected present-day climate diagnostics (precipitation, temperature, specific humidity and zonal wind) reveals biases consistent with state-of-the-art climate models. The model-to-model comparison of changes in temperature, specific humidity and zonal wind between 1850 and 2000 and between 2000 and 2100 indicates mostly consistent results. However, models that are clear outliers are different enough from the other models to significantly affect their simulation of atmospheric chemistry.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, Norway, France, Germany, France, NorwayPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYS. B. Dalsøren; Sarah A. Strode; Sarah A. Strode; Larry W. Horowitz; Ruth M. Doherty; David A. Plummer; Apostolos Voulgarakis; David Stevenson; Michael Schulz; Veronika Eyring; Gregory Faluvegi; Sophie Szopa; Y. H. Lee; Steven J. Ghan; Béatrice Josse; Ian A. MacKenzie; Philip Cameron-Smith; Paul Young; Paul Young; Paul Young; Ragnhild Bieltvedt Skeie; Drew Shindell; Dan Bergmann; Vaishali Naik; William J. Collins; William J. Collins; Guang Zeng; T. Nagashima; Gerd A. Folberth; S. T. Rumbold; Kengo Sudo; Irene Cionni; Mattia Righi; Jean-Francois Lamarque;Abstract. The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) consists of a series of time slice experiments targeting the long-term changes in atmospheric composition between 1850 and 2100, with the goal of documenting composition changes and the associated radiative forcing. In this overview paper, we introduce the ACCMIP activity, the various simulations performed (with a requested set of 14) and the associated model output. The 16 ACCMIP models have a wide range of horizontal and vertical resolutions, vertical extent, chemistry schemes and interaction with radiation and clouds. While anthropogenic and biomass burning emissions were specified for all time slices in the ACCMIP protocol, it is found that the natural emissions are responsible for a significant range across models, mostly in the case of ozone precursors. The analysis of selected present-day climate diagnostics (precipitation, temperature, specific humidity and zonal wind) reveals biases consistent with state-of-the-art climate models. The model-to-model comparison of changes in temperature, specific humidity and zonal wind between 1850 and 2000 and between 2000 and 2100 indicates mostly consistent results. However, models that are clear outliers are different enough from the other models to significantly affect their simulation of atmospheric chemistry.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
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description Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 Norway, France, United Kingdom, France, Norway, France, GermanyPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYDavid A. Plummer; Larry W. Horowitz; Oliver Wild; Ruth M. Doherty; Drew Shindell; Dan Bergmann; Vaishali Naik; Alexander T. Archibald; Sarah A. Strode; Sarah A. Strode; Gregory Faluvegi; Sophie Szopa; Philip Cameron-Smith; Irene Cionni; Béatrice Josse; Kengo Sudo; Apostolos Voulgarakis; Veronika Eyring; S. T. Rumbold; Ian A. MacKenzie; Simone Tilmes; Y. H. Lee; Ragnhild Bieltvedt Skeie; T. Nagashima; Kevin W. Bowman; Paul Young; Paul Young; Paul Young; William J. Collins; William J. Collins; Mattia Righi; Guang Zeng; Jean-Francois Lamarque; S. B. Dalsøren; David Stevenson;Abstract. Present day tropospheric ozone and its changes between 1850 and 2100 are considered, analysing 15 global models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The multi-model mean compares well against present day observations. The seasonal cycle correlates well, except for some locations in the tropical upper troposphere. Most (75%) of the models are encompassed with a range of global mean tropospheric ozone column estimates from satellite data, although there is a suggestion of a high bias in the Northern Hemisphere and a low bias in the Southern Hemisphere. Compared to the present day multi-model mean tropospheric ozone burden of 337 Tg, the multi-model mean burden for 1850 time slice is ~ 30% lower. Future changes were modelled using emissions and climate projections from four Representative Concentration Pathways (RCPs). Compared to 2000, the relative changes for the tropospheric ozone burden in 2030 (2100) for the different RCPs are: −5% (−22%) for RCP2.6, 3% (−8%) for RCP4.5, 0% (−9%) for RCP6.0, and 5% (15%) for RCP8.5. Model agreement on the magnitude of the change is greatest for larger changes. Reductions in precursor emissions are common across the RCPs and drive ozone decreases in all but RCP8.5, where doubled methane and a larger stratospheric influx increase ozone. Models with high ozone abundances for the present day also have high ozone levels for the other time slices, but there are no models consistently predicting large or small changes. Spatial patterns of ozone changes are well correlated across most models, but are notably different for models without time evolving stratospheric ozone concentrations. A unified approach to ozone budget specifications is recommended to help future studies attribute ozone changes and inter-model differences more clearly.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu514 citations 514 popularity Top 0.1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 Norway, France, United Kingdom, France, Norway, France, GermanyPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYDavid A. Plummer; Larry W. Horowitz; Oliver Wild; Ruth M. Doherty; Drew Shindell; Dan Bergmann; Vaishali Naik; Alexander T. Archibald; Sarah A. Strode; Sarah A. Strode; Gregory Faluvegi; Sophie Szopa; Philip Cameron-Smith; Irene Cionni; Béatrice Josse; Kengo Sudo; Apostolos Voulgarakis; Veronika Eyring; S. T. Rumbold; Ian A. MacKenzie; Simone Tilmes; Y. H. Lee; Ragnhild Bieltvedt Skeie; T. Nagashima; Kevin W. Bowman; Paul Young; Paul Young; Paul Young; William J. Collins; William J. Collins; Mattia Righi; Guang Zeng; Jean-Francois Lamarque; S. B. Dalsøren; David Stevenson;Abstract. Present day tropospheric ozone and its changes between 1850 and 2100 are considered, analysing 15 global models that participated in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The multi-model mean compares well against present day observations. The seasonal cycle correlates well, except for some locations in the tropical upper troposphere. Most (75%) of the models are encompassed with a range of global mean tropospheric ozone column estimates from satellite data, although there is a suggestion of a high bias in the Northern Hemisphere and a low bias in the Southern Hemisphere. Compared to the present day multi-model mean tropospheric ozone burden of 337 Tg, the multi-model mean burden for 1850 time slice is ~ 30% lower. Future changes were modelled using emissions and climate projections from four Representative Concentration Pathways (RCPs). Compared to 2000, the relative changes for the tropospheric ozone burden in 2030 (2100) for the different RCPs are: −5% (−22%) for RCP2.6, 3% (−8%) for RCP4.5, 0% (−9%) for RCP6.0, and 5% (15%) for RCP8.5. Model agreement on the magnitude of the change is greatest for larger changes. Reductions in precursor emissions are common across the RCPs and drive ozone decreases in all but RCP8.5, where doubled methane and a larger stratospheric influx increase ozone. Models with high ozone abundances for the present day also have high ozone levels for the other time slices, but there are no models consistently predicting large or small changes. Spatial patterns of ozone changes are well correlated across most models, but are notably different for models without time evolving stratospheric ozone concentrations. A unified approach to ozone budget specifications is recommended to help future studies attribute ozone changes and inter-model differences more clearly.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu514 citations 514 popularity Top 0.1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048074Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-21615-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2013 France, United Kingdom, France, France, Norway, Germany, NorwayPublisher:Copernicus GmbH Kengo Sudo; Gunnar Myhre; Ragnhild Bieltvedt Skeie; Tatsuya Nagashima; Terje Koren Berntsen; T. P. C. van Noije; Larry W. Horowitz; Sophie Szopa; Drew Shindell; Dan Bergmann; Vaishali Naik; Andrew Conley; Alexander T. Archibald; S. T. Rumbold; Y. H. Lee; Irene Cionni; Jean-Francois Lamarque; Sarah A. Strode; Sarah A. Strode; Ruth M. Doherty; David A. Plummer; Gerd A. Folberth; S. B. Dalsøren; Oliver Wild; Philip Cameron-Smith; Ian A. MacKenzie; Veronika Eyring; Béatrice Josse; A. Strunk; Kevin W. Bowman; Apostolos Voulgarakis; Mattia Righi; William J. Collins; William J. Collins; Paul Young; Paul Young; Paul Young; Guang Zeng; David Stevenson;Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2013 France, United Kingdom, France, France, Norway, Germany, NorwayPublisher:Copernicus GmbH Kengo Sudo; Gunnar Myhre; Ragnhild Bieltvedt Skeie; Tatsuya Nagashima; Terje Koren Berntsen; T. P. C. van Noije; Larry W. Horowitz; Sophie Szopa; Drew Shindell; Dan Bergmann; Vaishali Naik; Andrew Conley; Alexander T. Archibald; S. T. Rumbold; Y. H. Lee; Irene Cionni; Jean-Francois Lamarque; Sarah A. Strode; Sarah A. Strode; Ruth M. Doherty; David A. Plummer; Gerd A. Folberth; S. B. Dalsøren; Oliver Wild; Philip Cameron-Smith; Ian A. MacKenzie; Veronika Eyring; Béatrice Josse; A. Strunk; Kevin W. Bowman; Apostolos Voulgarakis; Mattia Righi; William J. Collins; William J. Collins; Paul Young; Paul Young; Paul Young; Guang Zeng; David Stevenson;Abstract. Ozone (O3) from 17 atmospheric chemistry models taking part in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) has been used to calculate tropospheric ozone radiative forcings (RFs). All models applied a common set of anthropogenic emissions, which are better constrained for the present-day than the past. Future anthropogenic emissions follow the four Representative Concentration Pathway (RCP) scenarios, which define a relatively narrow range of possible air pollution emissions. We calculate a value for the pre-industrial (1750) to present-day (2010) tropospheric ozone RF of 410 mW m−2. The model range of pre-industrial to present-day changes in O3 produces a spread (±1 standard deviation) in RFs of ±17%. Three different radiation schemes were used – we find differences in RFs between schemes (for the same ozone fields) of ±10%. Applying two different tropopause definitions gives differences in RFs of ±3%. Given additional (unquantified) uncertainties associated with emissions, climate-chemistry interactions and land-use change, we estimate an overall uncertainty of ±30% for the tropospheric ozone RF. Experiments carried out by a subset of six models attribute tropospheric ozone RF to increased emissions of methane (44±12%), nitrogen oxides (31 ± 9%), carbon monoxide (15 ± 3%) and non-methane volatile organic compounds (9 ± 2%); earlier studies attributed more of the tropospheric ozone RF to methane and less to nitrogen oxides. Normalising RFs to changes in tropospheric column ozone, we find a global mean normalised RF of 42 mW m−2 DU−1, a value similar to previous work. Using normalised RFs and future tropospheric column ozone projections we calculate future tropospheric ozone RFs (mW m−2; relative to 1750) for the four future scenarios (RCP2.6, RCP4.5, RCP6.0 and RCP8.5) of 350, 420, 370 and 460 (in 2030), and 200, 300, 280 and 600 (in 2100). Models show some coherent responses of ozone to climate change: decreases in the tropical lower troposphere, associated with increases in water vapour; and increases in the sub-tropical to mid-latitude upper troposphere, associated with increases in lightning and stratosphere-to-troposphere transport. Climate change has relatively small impacts on global mean tropospheric ozone RF.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen gold 352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048310Data sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-3063-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United States, France, Germany, United KingdomPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYGregory Faluvegi; Apostolos Voulgarakis; Apostolos Voulgarakis; Sophie Szopa; Béatrice Josse; Larry W. Horowitz; Ian A. MacKenzie; Robert D. Field; Robert D. Field; Oliver Wild; Drew Shindell; Dan Bergmann; Vaishali Naik; Gerd A. Folberth; S. B. Dalsøren; Tatsuya Nagashima; Guang Zeng; Michael J. Prather; S. T. Rumbold; Philip Cameron-Smith; David A. Plummer; Irene Cionni; David Stevenson; Sarah A. Strode; William J. Collins; William J. Collins; Ruth M. Doherty; Paul Young; Paul Young; Paul Young; Jean-Francois Lamarque; Veronika Eyring; Mattia Righi; Kengo Sudo;Abstract. Results from simulations performed for the Atmospheric Chemistry and Climate Modeling Intercomparison Project (ACCMIP) are analysed to examine how OH and methane lifetime may change from present-day to the future, under different climate and emissions scenarios. Present-day (2000) mean tropospheric chemical lifetime derived from the ACCMIP multi-model mean is 9.8 ± 1.6 yr, lower than a recent observationally-based estimate, but with a similar range to previous multi-model estimates. Future model projections are based on the four Representative Concentration Pathways (RCPs), and the results also exhibit a~large range. Decreases in global methane lifetime of 4.5 ± 9.1% are simulated for the scenario with lowest radiative forcing by 2100 (RCP 2.6), while increases of 8.5 ± 10.4% are simulated for the scenario with highest radiative forcing (RCP 8.5). In this scenario, the key driver of the evolution of OH and methane lifetime is methane itself, since its concentration more than doubles by 2100, and it consumes much of the OH that exists in the troposphere. Stratospheric ozone recovery, which drives tropospheric OH decreases through photolysis modifications, also plays a~partial role. In the other scenarios, where methane changes are less drastic, the interplay between various competing drivers leads to smaller and more diverse OH and methane lifetime responses, which are difficult to attribute. For all scenarios, regional OH changes are even more variable, with the most robust feature being the large decreases over the remote oceans in RCP 8.5. Through a~regression analysis, we suggest that differences in emissions of non-methane volatile organic compounds and in the simulation of photolysis rates may be the main factors causing the differences in simulated present-day OH and methane lifetime. Diversity in predicted changes between present-day and future was found to be associated more strongly with differences in modelled climate changes, specifically global temperature and humidity. Finally, through perturbation experiments we calculated an OH feedback factor (F) of 1.29 from present-day conditions (1.65 from 2100 RCP 8.5 conditions) and a~climate feedback on methane lifetime of 0.33 ± 0.13 yr K−1, on average.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu241 citations 241 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United States, France, Germany, United KingdomPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYGregory Faluvegi; Apostolos Voulgarakis; Apostolos Voulgarakis; Sophie Szopa; Béatrice Josse; Larry W. Horowitz; Ian A. MacKenzie; Robert D. Field; Robert D. Field; Oliver Wild; Drew Shindell; Dan Bergmann; Vaishali Naik; Gerd A. Folberth; S. B. Dalsøren; Tatsuya Nagashima; Guang Zeng; Michael J. Prather; S. T. Rumbold; Philip Cameron-Smith; David A. Plummer; Irene Cionni; David Stevenson; Sarah A. Strode; William J. Collins; William J. Collins; Ruth M. Doherty; Paul Young; Paul Young; Paul Young; Jean-Francois Lamarque; Veronika Eyring; Mattia Righi; Kengo Sudo;Abstract. Results from simulations performed for the Atmospheric Chemistry and Climate Modeling Intercomparison Project (ACCMIP) are analysed to examine how OH and methane lifetime may change from present-day to the future, under different climate and emissions scenarios. Present-day (2000) mean tropospheric chemical lifetime derived from the ACCMIP multi-model mean is 9.8 ± 1.6 yr, lower than a recent observationally-based estimate, but with a similar range to previous multi-model estimates. Future model projections are based on the four Representative Concentration Pathways (RCPs), and the results also exhibit a~large range. Decreases in global methane lifetime of 4.5 ± 9.1% are simulated for the scenario with lowest radiative forcing by 2100 (RCP 2.6), while increases of 8.5 ± 10.4% are simulated for the scenario with highest radiative forcing (RCP 8.5). In this scenario, the key driver of the evolution of OH and methane lifetime is methane itself, since its concentration more than doubles by 2100, and it consumes much of the OH that exists in the troposphere. Stratospheric ozone recovery, which drives tropospheric OH decreases through photolysis modifications, also plays a~partial role. In the other scenarios, where methane changes are less drastic, the interplay between various competing drivers leads to smaller and more diverse OH and methane lifetime responses, which are difficult to attribute. For all scenarios, regional OH changes are even more variable, with the most robust feature being the large decreases over the remote oceans in RCP 8.5. Through a~regression analysis, we suggest that differences in emissions of non-methane volatile organic compounds and in the simulation of photolysis rates may be the main factors causing the differences in simulated present-day OH and methane lifetime. Diversity in predicted changes between present-day and future was found to be associated more strongly with differences in modelled climate changes, specifically global temperature and humidity. Finally, through perturbation experiments we calculated an OH feedback factor (F) of 1.29 from present-day conditions (1.65 from 2100 RCP 8.5 conditions) and a~climate feedback on methane lifetime of 0.33 ± 0.13 yr K−1, on average.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu241 citations 241 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/640882kwData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048411Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefAtmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acpd-12-22945-2012&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, United States, United States, France, France, United States, United States, Norway, Norway, GermanyPublisher:Copernicus GmbH S. T. Rumbold; Gregory Faluvegi; Ian A. MacKenzie; Michael J. Prather; Y. H. Lee; Sophie Szopa; Larry W. Horowitz; Guang Zeng; Jean-Francois Lamarque; Kengo Sudo; T. P. C. van Noije; Meiyun Lin; Meiyun Lin; David Stevenson; Gerd A. Folberth; Ruth M. Doherty; Ragnhild Bieltvedt Skeie; Sarah A. Strode; Mattia Righi; William J. Collins; William J. Collins; Veronika Eyring; Béatrice Josse; Tatsuya Nagashima; Paul Young; Paul Young; Paul Young; Drew Shindell; Vaishali Naik; Arlene M. Fiore; David A. Plummer; Daniel Bergmann; Philip Cameron-Smith; S. B. Dalsøren; Irene Cionni; Apostolos Voulgarakis;Abstract. We have analysed time-slice simulations from 17 global models, participating in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), to explore changes in present-day (2000) hydroxyl radical (OH) concentration and methane (CH4) lifetime relative to preindustrial times (1850) and to 1980. A comparison of modeled and observation-derived methane and methyl chloroform lifetimes suggests that the present-day global multi-model mean OH concentration is overestimated by 5 to 10% but is within the range of uncertainties. The models consistently simulate higher OH concentrations in the Northern Hemisphere (NH) compared with the Southern Hemisphere (SH) for the present-day (2000; inter-hemispheric ratios of 1.13 to 1.42), in contrast to observation-based approaches which generally indicate higher OH in the SH although uncertainties are large. Evaluation of simulated carbon monoxide (CO) concentrations, the primary sink for OH, against ground-based and satellite observations suggests low biases in the NH that may contribute to the high north–south OH asymmetry in the models. The models vary widely in their regional distribution of present-day OH concentrations (up to 34%). Despite large regional changes, the multi-model global mean (mass-weighted) OH concentration changes little over the past 150 yr, due to concurrent increases in factors that enhance OH (humidity, tropospheric ozone, nitrogen oxide (NOx) emissions, and UV radiation due to decreases in stratospheric ozone), compensated by increases in OH sinks (methane abundance, carbon monoxide and non-methane volatile organic carbon (NMVOC) emissions). The large inter-model diversity in the sign and magnitude of preindustrial to present-day OH changes (ranging from a decrease of 12.7% to an increase of 14.6%) indicate that uncertainty remains in our understanding of the long-term trends in OH and methane lifetime. We show that this diversity is largely explained by the different ratio of the change in global mean tropospheric CO and NOx burdens (ΔCO/ΔNOx, approximately represents changes in OH sinks versus changes in OH sources) in the models, pointing to a need for better constraints on natural precursor emissions and on the chemical mechanisms in the current generation of chemistry-climate models. For the 1980 to 2000 period, we find that climate warming and a slight increase in mean OH (3.5 ± 2.2%) leads to a 4.3 ± 1.9% decrease in the methane lifetime. Analysing sensitivity simulations performed by 10 models, we find that preindustrial to present-day climate change decreased the methane lifetime by about four months, representing a negative feedback on the climate system. Further, we analysed attribution experiments performed by a subset of models relative to 2000 conditions with only one precursor at a time set to 1860 levels. We find that global mean OH increased by 46.4 ± 12.2% in response to preindustrial to present-day anthropogenic NOx emission increases, and decreased by 17.3 ± 2.3%, 7.6 ± 1.5%, and 3.1 ± 3.0% due to methane burden, and anthropogenic CO, and NMVOC emissions increases, respectively.
Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eu274 citations 274 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, United States, United States, France, France, United States, United States, Norway, Norway, GermanyPublisher:Copernicus GmbH S. T. Rumbold; Gregory Faluvegi; Ian A. MacKenzie; Michael J. Prather; Y. H. Lee; Sophie Szopa; Larry W. Horowitz; Guang Zeng; Jean-Francois Lamarque; Kengo Sudo; T. P. C. van Noije; Meiyun Lin; Meiyun Lin; David Stevenson; Gerd A. Folberth; Ruth M. Doherty; Ragnhild Bieltvedt Skeie; Sarah A. Strode; Mattia Righi; William J. Collins; William J. Collins; Veronika Eyring; Béatrice Josse; Tatsuya Nagashima; Paul Young; Paul Young; Paul Young; Drew Shindell; Vaishali Naik; Arlene M. Fiore; David A. Plummer; Daniel Bergmann; Philip Cameron-Smith; S. B. Dalsøren; Irene Cionni; Apostolos Voulgarakis;Abstract. We have analysed time-slice simulations from 17 global models, participating in the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), to explore changes in present-day (2000) hydroxyl radical (OH) concentration and methane (CH4) lifetime relative to preindustrial times (1850) and to 1980. A comparison of modeled and observation-derived methane and methyl chloroform lifetimes suggests that the present-day global multi-model mean OH concentration is overestimated by 5 to 10% but is within the range of uncertainties. The models consistently simulate higher OH concentrations in the Northern Hemisphere (NH) compared with the Southern Hemisphere (SH) for the present-day (2000; inter-hemispheric ratios of 1.13 to 1.42), in contrast to observation-based approaches which generally indicate higher OH in the SH although uncertainties are large. Evaluation of simulated carbon monoxide (CO) concentrations, the primary sink for OH, against ground-based and satellite observations suggests low biases in the NH that may contribute to the high north–south OH asymmetry in the models. The models vary widely in their regional distribution of present-day OH concentrations (up to 34%). Despite large regional changes, the multi-model global mean (mass-weighted) OH concentration changes little over the past 150 yr, due to concurrent increases in factors that enhance OH (humidity, tropospheric ozone, nitrogen oxide (NOx) emissions, and UV radiation due to decreases in stratospheric ozone), compensated by increases in OH sinks (methane abundance, carbon monoxide and non-methane volatile organic carbon (NMVOC) emissions). The large inter-model diversity in the sign and magnitude of preindustrial to present-day OH changes (ranging from a decrease of 12.7% to an increase of 14.6%) indicate that uncertainty remains in our understanding of the long-term trends in OH and methane lifetime. We show that this diversity is largely explained by the different ratio of the change in global mean tropospheric CO and NOx burdens (ΔCO/ΔNOx, approximately represents changes in OH sinks versus changes in OH sources) in the models, pointing to a need for better constraints on natural precursor emissions and on the chemical mechanisms in the current generation of chemistry-climate models. For the 1980 to 2000 period, we find that climate warming and a slight increase in mean OH (3.5 ± 2.2%) leads to a 4.3 ± 1.9% decrease in the methane lifetime. Analysing sensitivity simulations performed by 10 models, we find that preindustrial to present-day climate change decreased the methane lifetime by about four months, representing a negative feedback on the climate system. Further, we analysed attribution experiments performed by a subset of models relative to 2000 conditions with only one precursor at a time set to 1860 levels. We find that global mean OH increased by 46.4 ± 12.2% in response to preindustrial to present-day anthropogenic NOx emission increases, and decreased by 17.3 ± 2.3%, 7.6 ± 1.5%, and 3.1 ± 3.0% due to methane burden, and anthropogenic CO, and NMVOC emissions increases, respectively.
Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu274 citations 274 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down University of California: eScholarshipArticle . 2013License: CC BYFull-Text: https://escholarship.org/uc/item/9rs3g774Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Columbia University Academic CommonsArticle . 2013Full-Text: https://doi.org/10.7916/D8833RN9Data sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048333Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Atmospheric Chemistry and Physics (ACP)Article . 2013 . Peer-reviewedLicense: CC BYData sources: Crossrefhttps://doi.org/10.5194/acpd-1...Article . 2012 . Peer-reviewedLicense: CC BYData sources: CrossrefeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of CaliforniaeScholarship - University of CaliforniaArticle . 2013Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/acp-13-5277-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 France, France, France, Germany, United StatesPublisher:Royal Society of Chemistry (RSC) Fiore, Arlene; Naik, Vaishali; Spracklen, Dominick; Steiner, Allison; Unger, Nadine; Prather, Michael; Bergmann, Dan; Cameron-Smith, Philip; Cionni, Irene; Collins, William; Dalsøren, Stig; Eyring, Veronika; Folberth, Gerd; Ginoux, Paul; Horowitz, Larry; Josse, Béatrice; Lamarque, Jean-François; Mackenzie, Ian; Nagashima, Tatsuya; O'Connor, Fiona; Righi, Mattia; Rumbold, Steven; Shindell, Drew; Skeie, Ragnhild; Sudo, Kengo; Szopa, Sophie; Takemura, Toshihiko; Zeng, Guang;pmid: 22868337
Emissions of air pollutants and their precursors determine regional air quality and can alter climate. Climate change can perturb the long-range transport, chemical processing, and local meteorology that influence air pollution. We review the implications of projected changes in methane (CH4), ozone precursors (O3), and aerosols for climate (expressed in terms of the radiative forcing metric or changes in global surface temperature) and hemispheric-to-continental scale air quality. Reducing the O3 precursor CH4 would slow near-term warming by decreasing both CH4 and tropospheric O3. Uncertainty remains as to the net climate forcing from anthropogenic nitrogen oxide (NOx) emissions, which increase tropospheric O3 (warming) but also increase aerosols and decrease CH4 (both cooling). Anthropogenic emissions of carbon monoxide (CO) and non-CH4 volatile organic compounds (NMVOC) warm by increasing both O3 and CH4. Radiative impacts from secondary organic aerosols (SOA) are poorly understood. Black carbon emission controls, by reducing the absorption of sunlight in the atmosphere and on snow and ice, have the potential to slow near-term warming, but uncertainties in coincident emissions of reflective (cooling) aerosols and poorly constrained cloud indirect effects confound robust estimates of net climate impacts. Reducing sulfate and nitrate aerosols would improve air quality and lessen interference with the hydrologic cycle, but lead to warming. A holistic and balanced view is thus needed to assess how air pollution controls influence climate; a first step towards this goal involves estimating net climate impacts from individual emission sectors. Modeling and observational analyses suggest a warming climate degrades air quality (increasing surface O3 and particulate matter) in many populated regions, including during pollution episodes. Prior Intergovernmental Panel on Climate Change (IPCC) scenarios (SRES) allowed unconstrained growth, whereas the Representative Concentration Pathway (RCP) scenarios assume uniformly an aggressive reduction, of air pollutant emissions. New estimates from the current generation of chemistry–climate models with RCP emissions thus project improved air quality over the next century relative to those using the IPCC SRES scenarios. These two sets of projections likely bracket possible futures. We find that uncertainty in emission-driven changes in air quality is generally greater than uncertainty in climate-driven changes. Confidence in air quality projections is limited by the reliability of anthropogenic emission trajectories and the uncertainties in regional climate responses, feedbacks with the terrestrial biosphere, and oxidation pathways affecting O3 and SOA.
Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 415 citations 415 popularity Top 1% influence Top 1% impulse Top 0.1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 France, France, France, Germany, United StatesPublisher:Royal Society of Chemistry (RSC) Fiore, Arlene; Naik, Vaishali; Spracklen, Dominick; Steiner, Allison; Unger, Nadine; Prather, Michael; Bergmann, Dan; Cameron-Smith, Philip; Cionni, Irene; Collins, William; Dalsøren, Stig; Eyring, Veronika; Folberth, Gerd; Ginoux, Paul; Horowitz, Larry; Josse, Béatrice; Lamarque, Jean-François; Mackenzie, Ian; Nagashima, Tatsuya; O'Connor, Fiona; Righi, Mattia; Rumbold, Steven; Shindell, Drew; Skeie, Ragnhild; Sudo, Kengo; Szopa, Sophie; Takemura, Toshihiko; Zeng, Guang;pmid: 22868337
Emissions of air pollutants and their precursors determine regional air quality and can alter climate. Climate change can perturb the long-range transport, chemical processing, and local meteorology that influence air pollution. We review the implications of projected changes in methane (CH4), ozone precursors (O3), and aerosols for climate (expressed in terms of the radiative forcing metric or changes in global surface temperature) and hemispheric-to-continental scale air quality. Reducing the O3 precursor CH4 would slow near-term warming by decreasing both CH4 and tropospheric O3. Uncertainty remains as to the net climate forcing from anthropogenic nitrogen oxide (NOx) emissions, which increase tropospheric O3 (warming) but also increase aerosols and decrease CH4 (both cooling). Anthropogenic emissions of carbon monoxide (CO) and non-CH4 volatile organic compounds (NMVOC) warm by increasing both O3 and CH4. Radiative impacts from secondary organic aerosols (SOA) are poorly understood. Black carbon emission controls, by reducing the absorption of sunlight in the atmosphere and on snow and ice, have the potential to slow near-term warming, but uncertainties in coincident emissions of reflective (cooling) aerosols and poorly constrained cloud indirect effects confound robust estimates of net climate impacts. Reducing sulfate and nitrate aerosols would improve air quality and lessen interference with the hydrologic cycle, but lead to warming. A holistic and balanced view is thus needed to assess how air pollution controls influence climate; a first step towards this goal involves estimating net climate impacts from individual emission sectors. Modeling and observational analyses suggest a warming climate degrades air quality (increasing surface O3 and particulate matter) in many populated regions, including during pollution episodes. Prior Intergovernmental Panel on Climate Change (IPCC) scenarios (SRES) allowed unconstrained growth, whereas the Representative Concentration Pathway (RCP) scenarios assume uniformly an aggressive reduction, of air pollutant emissions. New estimates from the current generation of chemistry–climate models with RCP emissions thus project improved air quality over the next century relative to those using the IPCC SRES scenarios. These two sets of projections likely bracket possible futures. We find that uncertainty in emission-driven changes in air quality is generally greater than uncertainty in climate-driven changes. Confidence in air quality projections is limited by the reliability of anthropogenic emission trajectories and the uncertainties in regional climate responses, feedbacks with the terrestrial biosphere, and oxidation pathways affecting O3 and SOA.
Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.1039/c2cs35095e&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euAccess RoutesGreen bronze 415 citations 415 popularity Top 1% influence Top 1% impulse Top 0.1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Columbia University Academic CommonsArticle . 2012Full-Text: https://doi.org/10.7916/D8BK1BZ2Data sources: Bielefeld Academic Search Engine (BASE)Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)University of California: eScholarshipArticle . 2012License: CC BYFull-Text: https://escholarship.org/uc/item/9dq137rjData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2012Full-Text: https://hal.science/hal-03048247Data sources: Bielefeld Academic Search Engine (BASE)eScholarship - University of CaliforniaArticle . 2012Data sources: eScholarship - University of Californiaadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, Norway, France, Germany, France, NorwayPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYS. B. Dalsøren; Sarah A. Strode; Sarah A. Strode; Larry W. Horowitz; Ruth M. Doherty; David A. Plummer; Apostolos Voulgarakis; David Stevenson; Michael Schulz; Veronika Eyring; Gregory Faluvegi; Sophie Szopa; Y. H. Lee; Steven J. Ghan; Béatrice Josse; Ian A. MacKenzie; Philip Cameron-Smith; Paul Young; Paul Young; Paul Young; Ragnhild Bieltvedt Skeie; Drew Shindell; Dan Bergmann; Vaishali Naik; William J. Collins; William J. Collins; Guang Zeng; T. Nagashima; Gerd A. Folberth; S. T. Rumbold; Kengo Sudo; Irene Cionni; Mattia Righi; Jean-Francois Lamarque;Abstract. The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) consists of a series of time slice experiments targeting the long-term changes in atmospheric composition between 1850 and 2100, with the goal of documenting composition changes and the associated radiative forcing. In this overview paper, we introduce the ACCMIP activity, the various simulations performed (with a requested set of 14) and the associated model output. The 16 ACCMIP models have a wide range of horizontal and vertical resolutions, vertical extent, chemistry schemes and interaction with radiation and clouds. While anthropogenic and biomass burning emissions were specified for all time slices in the ACCMIP protocol, it is found that the natural emissions are responsible for a significant range across models, mostly in the case of ozone precursors. The analysis of selected present-day climate diagnostics (precipitation, temperature, specific humidity and zonal wind) reveals biases consistent with state-of-the-art climate models. The model-to-model comparison of changes in temperature, specific humidity and zonal wind between 1850 and 2000 and between 2000 and 2100 indicates mostly consistent results. However, models that are clear outliers are different enough from the other models to significantly affect their simulation of atmospheric chemistry.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
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For further information contact us at helpdesk@openaire.eu352 citations 352 popularity Top 1% influence Top 1% impulse Top 1% Powered by BIP!
more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.eudescription Publicationkeyboard_double_arrow_right Article , Other literature type , Journal 2012 United Kingdom, France, Norway, France, Germany, France, NorwayPublisher:Copernicus GmbH Funded by:UKRI | AIR POLLUTION AND WEATHER...UKRI| AIR POLLUTION AND WEATHER-RELATED HEALTH IMPACTS: METHODOLOGICAL STUDY BASED ON SPATIO-TEMPORALLY DISAGGREGATED MULTI-POLLUTANT MODELS FOR PRESENT-DAYS. B. Dalsøren; Sarah A. Strode; Sarah A. Strode; Larry W. Horowitz; Ruth M. Doherty; David A. Plummer; Apostolos Voulgarakis; David Stevenson; Michael Schulz; Veronika Eyring; Gregory Faluvegi; Sophie Szopa; Y. H. Lee; Steven J. Ghan; Béatrice Josse; Ian A. MacKenzie; Philip Cameron-Smith; Paul Young; Paul Young; Paul Young; Ragnhild Bieltvedt Skeie; Drew Shindell; Dan Bergmann; Vaishali Naik; William J. Collins; William J. Collins; Guang Zeng; T. Nagashima; Gerd A. Folberth; S. T. Rumbold; Kengo Sudo; Irene Cionni; Mattia Righi; Jean-Francois Lamarque;Abstract. The Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) consists of a series of time slice experiments targeting the long-term changes in atmospheric composition between 1850 and 2100, with the goal of documenting composition changes and the associated radiative forcing. In this overview paper, we introduce the ACCMIP activity, the various simulations performed (with a requested set of 14) and the associated model output. The 16 ACCMIP models have a wide range of horizontal and vertical resolutions, vertical extent, chemistry schemes and interaction with radiation and clouds. While anthropogenic and biomass burning emissions were specified for all time slices in the ACCMIP protocol, it is found that the natural emissions are responsible for a significant range across models, mostly in the case of ozone precursors. The analysis of selected present-day climate diagnostics (precipitation, temperature, specific humidity and zonal wind) reveals biases consistent with state-of-the-art climate models. The model-to-model comparison of changes in temperature, specific humidity and zonal wind between 1850 and 2000 and between 2000 and 2100 indicates mostly consistent results. However, models that are clear outliers are different enough from the other models to significantly affect their simulation of atmospheric chemistry.
Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
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more_vert Hyper Article en Lig... arrow_drop_down Université de Versailles Saint-Quentin-en-Yvelines: HAL-UVSQArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)Lancaster University: Lancaster EprintsArticle . 2013License: CC BYData sources: Bielefeld Academic Search Engine (BASE)Institut national des sciences de l'Univers: HAL-INSUArticle . 2013Full-Text: https://hal.science/hal-03048305Data sources: Bielefeld Academic Search Engine (BASE)https://doi.org/10.5194/gmdd-5...Article . 2012 . Peer-reviewedLicense: CC BYData sources: Crossrefadd ClaimPlease grant OpenAIRE to access and update your ORCID works.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.This Research product is the result of merged Research products in OpenAIRE.
You have already added works in your ORCID record related to the merged Research product.All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://beta.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=10.5194/gmd-6-179-2013&type=result"></script>'); --> </script>
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