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RESEARCH PRODUCT

Observations of atmospheric chemical deposition to high Arctic snow

David W. TarasickAndrew PlattLin HuangJonathan P. D. AbbattYing Duan LeiGreg J. EvansHeiko BozemJoseph R. McconnellNathan ChellmanSangeeta SharmaKatrina M. MacdonaldDesiree ToomAlina ChivulescuDaniel KunkelSarah J. HannaAllan K. BertramMike Elsasser

subject

Atmospheric Science010504 meteorology & atmospheric sciencesClimate changeCarbon black010501 environmental sciencesAtmospheric sciencesSnow01 natural scienceslcsh:QC1-999AerosolSedimentary depositional environmentlcsh:ChemistryDeposition (aerosol physics)Arcticlcsh:QD1-99913. Climate actionClimatologyEnvironmental scienceScavenginghuman activitieslcsh:Physics0105 earth and related environmental sciences

description

Abstract. Rapidly rising temperatures and loss of snow and ice cover have demonstrated the unique vulnerability of the high Arctic to climate change. There are major uncertainties in modelling the chemical depositional and scavenging processes of Arctic snow. To that end, fresh snow samples collected on average every 4 days at Alert, Nunavut, from September 2014 to June 2015 were analyzed for black carbon, major ions, and metals, and their concentrations and fluxes were reported. Comparison with simultaneous measurements of atmospheric aerosol mass loadings yields effective deposition velocities that encompass all processes by which the atmospheric species are transferred to the snow. It is inferred from these values that dry deposition is the dominant removal mechanism for several compounds over the winter while wet deposition increased in importance in the fall and spring, possibly due to enhanced scavenging by mixed-phase clouds. Black carbon aerosol was the least efficiently deposited species to the snow.

10.5194/acp-17-5775-2017http://www.atmos-chem-phys.net/17/5775/2017/acp-17-5775-2017.pdf