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dc.contributor.authorSafieddine, Sarah
dc.contributor.authorHeald, Colette L.
dc.date.accessioned2018-11-14T19:29:22Z
dc.date.available2018-11-14T19:29:22Z
dc.date.issued2017-11
dc.date.submitted2017-08
dc.identifier.issn0094-8276
dc.identifier.urihttp://hdl.handle.net/1721.1/119016
dc.description.abstractPrecipitation is the largest physical removal pathway of atmospheric reactive organic carbon in the form of dissolved organic carbon (DOC). We present the first global DOC distribution simulated with a global model. A total of 85 and 188 Tg C yr⁻¹ are deposited to the ocean and the land, respectively, with DOC ranging between 0.1 and 10 mg C L⁻¹ in this GEOS‐Chem simulation. We compare the 2010 simulated DOC to a 30 year synthesis of measurements. Despite limited measurements and imperfect temporal matching, the model is able to reproduce much of the spatial variability of DOC (r = 0.63), with a low bias of 35%. We present the global average carbon oxidation state (OS[overline][subscript c]) as a simple metric for describing the chemical composition. In the atmosphere, -1.8 ≤ OS[overline][subscript c] ≤ -0.6, and the increase in solubility upon oxidation leads to a global increase in (OS[overline][subscript c]) in precipitation with -0.6 ≤OS[overline][subscript c] ≤ 0. Keywords: dissolved organic carbon; average carbon oxidation state; GEOS-Chemen_US
dc.description.sponsorshipUnited States. National Oceanic and Atmospheric Administration (Grant NA14OAR4310132)en_US
dc.language.isoen_US
dc.publisherAmerican Geophysical Union (AGU)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/2017GL075270en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceProf. Heald via Elizabeth Soergelen_US
dc.titleA Global Assessment of Dissolved Organic Carbon in Precipitationen_US
dc.typeArticleen_US
dc.identifier.citationSafieddine, Sarah A. and Colette L. Heald. “A Global Assessment of Dissolved Organic Carbon in Precipitation.” Geophysical Research Letters 44, 22 (November 2017): 11,672–11,681 © 2017 American Geophysical Unionen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
dc.contributor.approverColette L. Healden_US
dc.contributor.mitauthorSafieddine, Sarah
dc.contributor.mitauthorHeald, Colette L.
dc.relation.journalGeophysical Research Lettersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsSafieddine, Sarah A.; Heald, Colette L.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8947-7950
dc.identifier.orcidhttps://orcid.org/0000-0003-2894-5738
mit.licensePUBLISHER_POLICYen_US


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