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dc.contributor.authorRuiz, Daniel J.
dc.contributor.authorPrather, Michael J.
dc.contributor.authorStrahan, Susan E.
dc.contributor.authorThompson, Rona Louise
dc.contributor.authorFroidevaux, Lucien
dc.contributor.authorSteenrod, Stephen D.
dc.date.accessioned2021-10-07T11:19:33Z
dc.date.available2021-10-07T11:19:33Z
dc.date.created2021-07-08T09:32:33Z
dc.date.issued2021
dc.identifier.citationJournal of Geophysical Research (JGR): Atmospheres. 2021, 126, e2020JD033979.en_US
dc.identifier.issn2169-897X
dc.identifier.urihttps://hdl.handle.net/11250/2788379
dc.description.abstractNitrous oxide (N2O) is a long-lived greenhouse gas that affects atmospheric chemistry and climate. In this work, we use satellite measurements of N2O, ozone (O3), and temperature from the Aura Microwave Limb Sounder (MLS) instrument to calculate stratospheric loss of N2O, and thus its atmospheric lifetime. Using three chemistry transport models simulating the Aura period 2005–2017, we verify the stratospheric sink using MLS data and follow that loss signal down to the surface and compare with surface observations. Stratospheric loss has a strong seasonal cycle and is further modulated by the Quasi-Biennial Oscillation (QBO); these cycles are seen equally in both observations and the models. When filtered for interannual variability, the modeled surface signal is QBO-caused, and it reproduces the observed pattern, highlighting the potential role of the QBO in tropospheric chemistry and composition, as well as in model evaluation. The observed annual surface signal in the northern hemisphere matches well with the models run without emissions, indicating the annual cycle is driven mostly by stratosphere-troposphere exchange (STE) flux of N2O-depleted air and not surface N2O emissions. In the southern hemisphere (SH), all three models disagree and thus provide no guidance, except for indicating that modeling annual STE in the SH remains a major model uncertainty. Parallel model simulations of CFCl3, which has greater stratospheric loss that N2O and possibly surreptitious emissions, show that its interannual variations parallel those of N2O, and thus the observed N2O variability can identify the stratospheric component of the observed CFCl3 variability.en_US
dc.language.isoengen_US
dc.titleHow Atmospheric Chemistry and Transport Drive Surface Variability of N2O and CFC-11en_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021. American Geophysical Union.en_US
dc.source.pagenumber16en_US
dc.source.volume126en_US
dc.source.journalJournal of Geophysical Research (JGR): Atmospheresen_US
dc.identifier.doi10.1029/2020JD033979
dc.identifier.cristin1920909
dc.relation.projectNILU: 119073en_US
dc.source.articlenumbere2020JD033979en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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