Hide metadata

dc.date.accessioned2024-03-03T18:33:47Z
dc.date.available2024-03-03T18:33:47Z
dc.date.created2023-06-01T13:07:56Z
dc.date.issued2023
dc.identifier.citationGallo, Francesca Sanchez, Kevin J. Anderson, Bruce E. Bennett, Ryan Brown, Matthew D. Crosbie, Ewan C. Hostetler, Chris Jordan, Carolyn Yang Martin, Melissa Robinson, Claire E. Russell, Lynn M. Shingler, Taylor J. Shook, Michael A. Thornhill, Kenneth L. Wiggins, Elizabeth B. Winstead, Edward L. Wisthaler, Armin Ziemba, Luke D. Moore, Richard H. . Measurement report: Aerosol vertical profiles over the western North Atlantic Ocean during the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES). Atmospheric Chemistry and Physics (ACP). 2023, 23(2), 1465-1490
dc.identifier.urihttp://hdl.handle.net/10852/108978
dc.description.abstractThe NASA North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) ship and aircraft field campaign deployed to the western subarctic Atlantic between the years 2015 and 2018. One of the primary goals of NAAMES is to improve the understanding of aerosol–cloud interaction (ACI) over the Atlantic Ocean under different seasonal regimes. ACIs currently represent the largest source of uncertainty in global climate models. During three NAAMES field campaigns (NAAMES-1 in November 2015, NAAMES-2 in May 2016, and NAAMES-3 in September 2017), multiple 10 h science flights were conducted using the NASA C-130 aircraft to measure marine boundary layer aerosol and cloud properties. The standard flight pattern includes vertical spirals where the C-130 transitioned from high altitude to low altitude (and vice versa), collecting in situ measurements of aerosols, trace gases, clouds, and meteorological parameters as a function of altitude. We examine the data collected from 37 spirals during the three NAAMES field campaigns, and we present a comprehensive characterization of the vertical profiles of aerosol properties under different synoptic conditions and aerosol regimes. The vertical distribution of submicron aerosol particles exhibited strong seasonal variation, as well as elevated intra-seasonal variability depending on emission sources and aerosol processes in the atmospheric column. Pristine marine conditions and new particle formation were prevalent in the wintertime (NAAMES-1) due to low biogenic emissions from the surface ocean and reduced continental influence. Higher concentrations of submicron aerosol particles were observed in the spring (NAAMES-2) due to strong phytoplankton activity and the arrival of long-range-transported continental plumes in the free troposphere with subsequent entrainment into the marine boundary layer. Biomass burning from boreal wildfires was the main source of aerosol particles in the region during the late summer (NAAMES-3) in both the marine boundary layer and free troposphere.
dc.languageEN
dc.publisherCopernicus GmbH
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMeasurement report: Aerosol vertical profiles over the western North Atlantic Ocean during the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES)
dc.title.alternativeENEngelskEnglishMeasurement report: Aerosol vertical profiles over the western North Atlantic Ocean during the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES)
dc.typeJournal article
dc.creator.authorGallo, Francesca
dc.creator.authorSanchez, Kevin J.
dc.creator.authorAnderson, Bruce E.
dc.creator.authorBennett, Ryan
dc.creator.authorBrown, Matthew D.
dc.creator.authorCrosbie, Ewan C.
dc.creator.authorHostetler, Chris
dc.creator.authorJordan, Carolyn
dc.creator.authorYang Martin, Melissa
dc.creator.authorRobinson, Claire E.
dc.creator.authorRussell, Lynn M.
dc.creator.authorShingler, Taylor J.
dc.creator.authorShook, Michael A.
dc.creator.authorThornhill, Kenneth L.
dc.creator.authorWiggins, Elizabeth B.
dc.creator.authorWinstead, Edward L.
dc.creator.authorWisthaler, Armin
dc.creator.authorZiemba, Luke D.
dc.creator.authorMoore, Richard H.
cristin.unitcode185,15,12,0
cristin.unitnameKjemisk institutt
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2150825
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Atmospheric Chemistry and Physics (ACP)&rft.volume=23&rft.spage=1465&rft.date=2023
dc.identifier.jtitleAtmospheric Chemistry and Physics (ACP)
dc.identifier.volume23
dc.identifier.issue2
dc.identifier.startpage1465
dc.identifier.endpage1490
dc.identifier.doihttps://doi.org/10.5194/acp-23-1465-2023
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1680-7316
dc.type.versionPublishedVersion


Files in this item

Appears in the following Collection

Hide metadata

Attribution 4.0 International
This item's license is: Attribution 4.0 International