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dc.contributor.authorGoodwin, Philip
dc.contributor.authorOmta, Anne Willem
dc.contributor.authorFollows, Michael J
dc.date.accessioned2018-10-03T15:54:24Z
dc.date.available2018-10-03T15:54:24Z
dc.date.issued2010-07
dc.date.submitted2010-03
dc.identifier.issn08866236
dc.identifier.urihttp://hdl.handle.net/1721.1/118341
dc.description.abstractNumerical studies have indicated that the steady-state ocean-atmosphere partitioning of carbon will change profoundly as emissions continue. In particular, the globally averaged Revelle buffer factor will first increase and then decrease at higher emissions. Furthermore, atmospheric carbon will initially grow exponentially with emission size, after which it will depend linearly on emissions at higher emission totals. In this article, we explain this behavior by means of an analytical theory based on simple carbonate chemistry. A cornerstone of the theory is a newly defined dimensionless factor, O. We show that the qualitative changes are connected with different regimes in ocean chemistry: if the air-sea partitioning of carbon is determined by the carbonate ion, then the Revelle factor increases with emissions, whereas the buffer factor decreases with emission size, when dissolved carbon dioxide determines the partitioning. Currently, the ocean carbonate chemistry is dominated by the carbonate ion response, but at high total emissions, the response of dissolved carbon dioxide takes on this role.en_US
dc.publisherAmerican Geophysical Union (AGU)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1029/2009GB003726en_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.sourceOther repositoryen_US
dc.titleMultiple regimes of air-sea carbon partitioning identified from constant-alkalinity buffer factorsen_US
dc.typeArticleen_US
dc.identifier.citationOmta, Anne Willem et al. “Multiple Regimes of Air-Sea Carbon Partitioning Identified from Constant-Alkalinity Buffer Factors.” Global Biogeochemical Cycles 24, 3 (July 2010): GB3008 © 2010 American Geophysical Unionen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciencesen_US
dc.contributor.mitauthorOmta, Anne Willem
dc.contributor.mitauthorFollows, Michael J
dc.relation.journalGlobal Biogeochemical Cyclesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-09-24T16:12:56Z
dspace.orderedauthorsOmta, Anne Willem; Goodwin, Philip; Follows, Michael J.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3102-0341
mit.licensePUBLISHER_POLICYen_US


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