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송창근

Song, Chang-Keun
Air Quality Impact Assessment Research Lab.
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dc.citation.endPage 115 -
dc.citation.startPage 103 -
dc.citation.title ATMOSPHERIC ENVIRONMENT -
dc.citation.volume 101 -
dc.contributor.author Kim, Minjoong J. -
dc.contributor.author Park, Rokjin J. -
dc.contributor.author Ho, Chang-Hoi -
dc.contributor.author Woo, Jung-Hun -
dc.contributor.author Choi, Ki-Chul -
dc.contributor.author Song, Chang-Keun -
dc.contributor.author Lee, Jae-Bum -
dc.date.accessioned 2023-12-22T01:42:14Z -
dc.date.available 2023-12-22T01:42:14Z -
dc.date.created 2016-12-07 -
dc.date.issued 2015-01 -
dc.description.abstract We investigate ozone air quality changes in 2050 caused by global changes in climate and anthropogenic emissions of ozone precursors by using a global chemical transport model driven by meteorological fields from a general circulation model. We use projected emissions based on the Representative Concentration Pathway (RCP) scenarios and conduct model simulations to quantify the effects of climate and emission changes on future air quality, focusing on ozone in surface air. Our model results show that annual mean concentrations of surface ozone will be lower in 2050 relative to 2000 by -3.3, -3.7, and -4.2 ppbv under RCP6.0, RCP4.5, and RCP2.6, respectively. In contrast, the RCP8.5 projection results in a slight increase of 2.1 ppbv caused by a methane increase. The ozone reductions are driven primarily by decreases in NOx emission, which dominate the climate penalty on ozone driven by temperature increases. We also estimate the effect of 21st century climate change on ozone air quality, assuming no changes in anthropogenic emissions of ozone precursors in the future. We further use a statistical method to analyze the results in order to quantify the effect of each meteorological variable change on ozone concentration in summer. Temperature increase is found to result in ozone increases of up to 2.2 ppbv over land. Ozone over the oceans, however, is largely reduced with specific humidity increase, particularly in the Northern Hemisphere, where the ozone concentration decreases by 0.8 ppbv. We find that future increases in natural NOx emissions from lightning and soil make an important contribution to the formation of nitric acid and might seriously offset future decreases in nitrogen deposition caused by anthropogenic NOx emission reduction. -
dc.identifier.bibliographicCitation ATMOSPHERIC ENVIRONMENT, v.101, pp.103 - 115 -
dc.identifier.doi 10.1016/j.atmosenv.2014.11.016 -
dc.identifier.issn 1352-2310 -
dc.identifier.scopusid 2-s2.0-84910655198 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/20951 -
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S1352231014008759 -
dc.identifier.wosid 000348017000012 -
dc.language 영어 -
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD -
dc.title Future ozone and oxidants change under the RCP scenarios -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Climate change -
dc.subject.keywordAuthor Ozone air quality -
dc.subject.keywordAuthor RCP -
dc.subject.keywordPlus INTERCOMPARISON PROJECT ACCMIP -
dc.subject.keywordPlus PARTICULATE MATTER PM2.5 -
dc.subject.keywordPlus REPRESENTATIVE CONCENTRATION PATHWAYS -
dc.subject.keywordPlus UNITED-STATES IMPLICATIONS -
dc.subject.keywordPlus CLIMATE-CHANGE -
dc.subject.keywordPlus SURFACE OZONE -
dc.subject.keywordPlus AIR-QUALITY -
dc.subject.keywordPlus TROPOSPHERIC OZONE -
dc.subject.keywordPlus ATMOSPHERIC CHEMISTRY -
dc.subject.keywordPlus METEOROLOGICAL MODES -

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