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dc.contributor.authorWang, Peidong
dc.contributor.authorScott, Jeffery R
dc.contributor.authorSolomon, Susan
dc.contributor.authorMarshall, John
dc.contributor.authorBabbin, Andrew R
dc.contributor.authorLickley, Megan
dc.contributor.authorThompson, David WJ
dc.contributor.authorDeVries, Timothy
dc.contributor.authorLiang, Qing
dc.contributor.authorPrinn, Ronald G
dc.date.accessioned2022-01-18T20:13:08Z
dc.date.available2021-10-27T19:53:52Z
dc.date.available2022-01-18T20:13:08Z
dc.date.issued2021
dc.identifier.issn1091-6490
dc.identifier.issn0027-8424
dc.identifier.urihttps://hdl.handle.net/1721.1/133626.2
dc.description.abstract© 2021 National Academy of Sciences. All rights reserved. The ocean is a reservoir for CFC-11, a major ozone-depleting chemical. Anthropogenic production of CFC-11 dramatically decreased in the 1990s under the Montreal Protocol, which stipulated a global phase out of production by 2010. However, studies raise questions about current overall emission levels and indicate unexpected increases of CFC-11 emissions of about 10 Gg · yr−1 after 2013 (based upon measured atmospheric concentrations and an assumed atmospheric lifetime). These findings heighten the need to understand processes that could affect the CFC-11 lifetime, including ocean fluxes. We evaluate how ocean uptake and release through 2300 affects CFC-11 lifetimes, emission estimates, and the long-term return of CFC-11 from the ocean reservoir. We show that ocean uptake yields a shorter total lifetime and larger inferred emission of atmospheric CFC-11 from 1930 to 2075 compared to estimates using only atmospheric processes. Ocean flux changes over time result in small but not completely negligible effects on the calculated unexpected emissions change (decreasing it by 0.4 ± 0.3 Gg · yr−1). Moreover, it is expected that the ocean will eventually become a source of CFC-11, increasing its total lifetime thereafter. Ocean outgassing should produce detectable increases in global atmospheric CFC-11 abundances by the mid-2100s, with emission of around 0.5 Gg · yr−1; this should not be confused with illicit production at that time. An illustrative model projection suggests that climate change is expected to make the ocean a weaker reservoir for CFC-11, advancing the detectable change in the global atmospheric mixing ratio by about 5 yr.en_US
dc.language.isoen
dc.publisherNational Academy of Sciencesen_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/PNAS.2021528118en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePNASen_US
dc.titleOn the effects of the ocean on atmospheric CFC-11 lifetimes and emissionsen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences
dc.relation.journalProceedings of the National Academy of Sciencesen_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.updated2021-09-13T18:14:09Z
dspace.orderedauthorsWang, P; Scott, JR; Solomon, S; Marshall, J; Babbin, AR; Lickley, M; Thompson, DWJ; DeVries, T; Liang, Q; Prinn, RGen_US
dspace.date.submission2021-09-13T18:14:11Z
mit.journal.volume118en_US
mit.journal.issue12en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work Neededen_US


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