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dc.contributor.advisorSusan Solomon.en_US
dc.contributor.authorMin, Floraen_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences.en_US
dc.coverage.spatiala------ n-us---en_US
dc.date.accessioned2015-02-25T17:10:28Z
dc.date.available2015-02-25T17:10:28Z
dc.date.copyright2014en_US
dc.date.issued2014en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/95565
dc.descriptionThesis: S.M. in Atmospheric Science, Massachusetts Institute of Technology, Department of Earth, Atmospheric, and Planetary Sciences, 2014.en_US
dc.descriptionIn title on title-page. double-underscored "x" appears as subscript. Cataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 42-49).en_US
dc.description.abstractA 3-D chemical transport model with coupled oxidant-aerosol chemistry (GEOSChem) is used to analyze the influence of recent (2001 to 2010) growth in Asian NOx and Asian SO 2 emission on transpacific transport of Asian particulate matter, especially sulfate, by quantifying and analyzing the details of chemistry and its sequential influence on transpacific transport during spring and summer. From 2001 to 2010, the spring averaged Asian sulfate enhancement in the western US model surface layer increases by 0.01-0.03 [mu]g M-3 (about 4% of the surface sulfate concentration over the US at 2010 emission level). The net chemical production rate increases in the troposphere over Asia but decreases over the Pacific Ocean. The sulfate production pathway shifts toward gas phase production by OH (7-8% increase-China; 2-3% increase-Upper atmosphere Pacific Ocean) with corresponding reductions in aqueous phase production by H202 ; resulting in a switch of the most important production pathway from aqueous production by H202 to gas phase production by OH. Almost doubling the Asian NO. emission during the period has a negligible influence on Asian sulfate enhancement over the US; this change in Asian NOx emission causes the net chemical production rate to increase in the Asian boundary layer, but to decrease in the upper Asian atmosphere, and in the atmosphere over the Pacific Ocean and the US. This is because the Asian NOx emission growth strengthens the oxidizing power in the Asian boundary layer to more actively form sulfate (mostly removed by wet scavenging), reducing available SO2 for further production away from the source. The Asian NOx emission growth is the major driver in changing the sulfate production pathways toward the gas phase. The 20% increase in Asian SO 2 emission during the period is the primary driver in increasing Asian sulfate enhancement over the US; this change accelerates net sulfate production rate, and makes a minor contribution to shifting toward gas phase production by OH over the course of the transpacific transport. The calculated sulfate column burden shows a notable increase as a response to the changes in Asian emissions. However, the shifts in sulfate lifetime over China due to changes in Asian SO 2 and/or Asian NO, emission are almost negligible (generally 1-2%), and lifetimes over the upper level Pacific Ocean are generally reduced by 3-4%.en_US
dc.description.statementofresponsibilityby Flora Min.en_US
dc.format.extent49 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectEarth, Atmospheric, and Planetary Sciences.en_US
dc.titleInfluence of recent Asian SO₂ and Asian NOx̳ emissions change (2001 to 2010) on particulate matter : shifts in Asian sulfate enhancement over US surface, major production pathway, and lifetimeen_US
dc.typeThesisen_US
dc.description.degreeS.M. in Atmospheric Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences
dc.identifier.oclc903537356en_US


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