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dc.contributor.advisorNoelle Selin.en_US
dc.contributor.authorRutkowski, Emma.en_US
dc.contributor.otherMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences.en_US
dc.coverage.spatialn-us-maen_US
dc.date.accessioned2019-10-04T21:34:59Z
dc.date.available2019-10-04T21:34:59Z
dc.date.copyright2019en_US
dc.date.issued2019en_US
dc.identifier.urihttps://hdl.handle.net/1721.1/122444
dc.descriptionThesis: S.B., Massachusetts Institute of Technology, Department of Earth, Atmospheric, and Planetary Sciences, 2019en_US
dc.descriptionPage 57 blank. Cataloged from PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (pages 48-52).en_US
dc.description.abstractThis study aims to contribute to the body of knowledge regarding mercury emissions by reporting on a coastal, urban setting subject to inputs from both anthropogenic and oceanic reservoirs, in order to improve related policy decisions. Mercury can have serious health and ecological consequences, but the chemistry, transport and deposition of gaseous elemental mercury (Hg0) are still not well understood. Estimates of anthropogenic emissions also remain uncertain. To better constrain urban- and regional-scale chemistry and emissions in a specifically coastal environment, concentrations of Hg0 were measured at an urban site in Boston, MA from Aug 2017 to Sept 2018. The recorded concentrations were compared against supplementary records of several additional pollutants and meteorological variables. Concentrations in Boston were found to be relatively low, but follow diurnal and seasonal trends previously observed in other sites in the United States driven by meteorology. Further, back-trajectory and potential source contribution function analysis revealed oceanic re-emission of legacy deposits is a major input of Hg0 to the Boston area, but no influence from specific large anthropogenic point sources was discernible in the data. A one box model was developed to represent the physical processes controlling Hg0 concentrations in Boston in order to replicate concentrations, capture the difference in concentrations from land and ocean sources, and estimate both anthropogenic and oceanic emissions. Results from the box model analysis show the sensitivity of local Hg0 concentrations to varying assumptions of mixing, background flux, meteorology, and emissions, and indicate that oceanic emissions and anthropogenic emissions are likely both higher than current estimates. The results of this study indicate the ocean plays a major role in Hg0 cycling in coastal areas and provides motivation for further improvement of models to better capture local sources and cycling.en_US
dc.description.statementofresponsibilityby Emma Rutkowski.en_US
dc.format.extent57 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.subjectEarth, Atmospheric, and Planetary Sciences.en_US
dc.titleCoastal urban atmospheric mercury cycling and emissions in Boston, MAen_US
dc.typeThesisen_US
dc.description.degreeS.B.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.identifier.oclc1120769379en_US
dc.description.collectionS.B. Massachusetts Institute of Technology, Department of Earth, Atmospheric, and Planetary Sciencesen_US
dspace.imported2019-10-04T21:34:55Zen_US
mit.thesis.degreeBacheloren_US
mit.thesis.departmentEAPSen_US


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