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dc.contributor.advisorColette L. Heald.en_US
dc.contributor.authorSu, Flora K. (Flora Kathleen)en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Civil and Environmental Engineering.en_US
dc.date.accessioned2018-05-23T16:34:42Z
dc.date.available2018-05-23T16:34:42Z
dc.date.copyright2018en_US
dc.date.issued2018en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/115784
dc.descriptionThesis: M. Eng., Massachusetts Institute of Technology, Department of Civil and Environmental Engineering, 2018.en_US
dc.descriptionCataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 38-42).en_US
dc.description.abstractOver the past century, global wildfire activity has intensified due to increasing mean temperatures. However, emissions inventories used for modeling the impact of fires on air quality and climate exhibit several discrepancies in emissions estimates, largely due to the different types of satellite products used for identifying fires and measuring burned area, as well as differences in emission factors describing the vegetative fuels burned. Using the GEOS-Chem v1 1-01 chemical transport model, we studied how differences in emissions estimates between two commonly-used global biomass burning inventories, the Global Fire Emissions Database (GFED4) and the Fire INventory from NCAR (FINNy 1), affects modeled concentrations of carbon monoxide (CO), nitrogen oxide (NO), black carbon (BC) aerosol, and organic carbon (OC) aerosol. We find that biomass burning emissions significantly impacted concentrations of CO, BC, and OC over the U.S., and that the estimated seasonal impact of fires differed between the FINN and GFED inventories. Simulations using FINN predict higher fire emissions and consequently, a greater impact on springtime concentrations of CO (~10% higher than GFED), BC (~20% higher), and OC (-30% higher). GFED, on the other hand, attributes a greater contribution of fires to summertime emissions, with 60 to 90% of yearly fire emissions occurring during the summer months versus 35 to 70% as estimated by FINN. During years with intensive summer wildfires, simulations using GFED exhibited a higher contribution of fires from the Western U.S. and the Canadian Northwest Territories to total CO (30%), BC (50%), and OC (70%) concentrations across the Northern U.S. Simulations using FINN, which estimated higher emissions during the fall/winter, showed a much smaller contribution of summer fires to concentrations in the Northern U.S. (25% CO, 25% BC, 50% OC), but a higher contribution during the fall and winter (20% CO, 15 to 25% BC, 40 to 50% OC. This analysis thus shows that the choice of biomass burning emissions inventory can have a significant impact on the modeled impact of fires on atmospheric composition - FINN estimates a larger impact from smoldering fires, whereas GFED estimates a greater contribution from flaming combustion.en_US
dc.description.statementofresponsibilityby Flora K. Su.en_US
dc.format.extent66 pagesen_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsMIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectCivil and Environmental Engineering.en_US
dc.titleInvestigating the effect of variability in biomass burning emissions inventories on GEOS-Chem modeled trace gas and aerosol concentrationsen_US
dc.typeThesisen_US
dc.description.degreeM. Eng.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineering
dc.identifier.oclc1036987800en_US


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