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dc.contributor.authorBrowse, J
dc.contributor.authorCarslaw, KS
dc.contributor.authorArnold, SR
dc.contributor.authorPringle, K
dc.contributor.authorBoucher, O
dc.date.accessioned2018-07-31T12:30:24Z
dc.date.issued2012-08-01
dc.description.abstractThe seasonal cycle in Arctic aerosol is typified by high concentrations of large aged anthropogenic particles transported from lower latitudes in the late Arctic winter and early spring followed by a sharp transition to low concentrations of locally sourced smaller particles in the summer. However, multi-model assessments show that many models fail to simulate a realistic cycle. Here, we use a global aerosol microphysics model (GLOMAP) and surface-level aerosol observations to understand how wet scavenging processes control the seasonal variation in Arctic black carbon (BC) and sulphate aerosol. We show that the transition from high wintertime concentrations to low concentrations in the summer is controlled by the transition from ice-phase cloud scavenging to the much more efficient warm cloud scavenging in the late spring troposphere. This seasonal cycle is amplified further by the appearance of warm drizzling cloud in the late spring and summer boundary layer. Implementing these processes in GLOMAP greatly improves the agreement between the model and observations at the three Arctic ground-stations Alert, Barrow and Zeppelin Mountain on Svalbard. The SO4 model-observation correlation coefficient (R) increases from:-0.33 to 0.71 at Alert (82.5 N), from-0.16 to 0.70 at Point Barrow (71.0 N) and from-0.42 to 0.40 at Zeppelin Mountain (78 N). The BC model-observation correlation coefficient increases from-0.68 to 0.72 at Alert and from-0.42 to 0.44 at Barrow. Observations at three marginal Arctic sites (Janiskoski, Oulanka and Karasjok) indicate a far weaker aerosol seasonal cycle, which we show is consistent with the much smaller seasonal change in the frequency of ice clouds compared to higher latitude sites. Our results suggest that the seasonal cycle in Arctic aerosol is driven by temperature-dependent scavenging processes that may be susceptible to modification in a future climate. © 2012 Author(s).en_GB
dc.description.sponsorshipJB was funded by a studentship from the Natural Environment Research Council and by the Met Office through a CASE partnership. KC is a Royal Society Wolfson Merit Award holder. We would like to thank Neil Gordon for providing low cloud satellite climatologies from the MODIS satellite and Dr Graham Mann for his comments and assistance. The authors acknowledge the Canadian National Atmospheric Chemistry (NAtChem) Database and its data contributing agencies/ organizations for the provision of the Sulphate mass data for the years 2000–2002, used in this publication. The agency responsible for all data contributions from the the NAtChem Database is the Canadian Arctic aerosol programme. The authors acknowledge and thank the scientists and data-providers of the Norwegian institute of air research (NILU), the National ocean and atmospheric administration (NOAA) and the EMEP observation network for the provision of BC and sulphate mass data used in this publication.en_GB
dc.identifier.citationVol. 12, pp. 6775 - 6798en_GB
dc.identifier.doi10.5194/acp-12-6775-2012
dc.identifier.urihttp://hdl.handle.net/10871/33606
dc.language.isoenen_GB
dc.publisherEuropean Geosciences Union (EGU)en_GB
dc.rights© Author(s) 2012. This work is distributed under the Creative Commons Attribution 3.0 License.en_GB
dc.titleThe scavenging processes controlling the seasonal cycle in Arctic sulphate and black carbon aerosolen_GB
dc.typeArticleen_GB
dc.date.available2018-07-31T12:30:24Z
dc.identifier.issn1680-7316
dc.descriptionThis is the final version of the article. Available from European Geosciences Union via the DOI in this record.en_GB
dc.identifier.journalAtmospheric Chemistry and Physicsen_GB


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