Atmospheric deposition of chemical species to polar snow

C. I. Davidson, M. H. Bergin, H. D. Kuhns

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Particles and gases can deposit from the atmosphere to polar snow by several mechanisms. Dry deposition can be considered to consist of three steps: aerodynamic transport from the free atmosphere to the viscous sublayer near the surface, boundary layer transport across the sublayer, and interactions with the surface. The particle dry deposition mass flux is dominated by the largest particles present in a size distribution. Wet deposition includes in-cloud and below-cloud scavenging, where the former refers to uptake of particles during nucleation of cloudwater as well as scavenging of particles and gases by existing droplets and ice crystals. Of all the wet deposition mechanisms, nucleation scavenging is often the most important mechanism for particles in the polar regions. Finally, incorporation of particles and gases into fog droplets and subsequent settling of the fog to the snow surface can be an important removal process in regions of frequent fog. For Summit, Greenland, the total deposition of MSA, SO42+, Na +, K + and Ca2+ during May 24-July 13, 1993 was dominated by wet deposition: this mechanism accounted for an average of 62% of the total deposition for these species. Fog and dry deposition accounted for 21% and 17% of the total, respectively. These results suggest that all three mechanisms may need to be considered when estimating total deposition of certain chemical species to polar snow.

Original languageEnglish (US)
Pages (from-to)227-249
Number of pages23
JournalChemical Engineering Communications
Volume151
DOIs
StatePublished - Jan 1 1996
Externally publishedYes

Keywords

  • Atmospheric deposition
  • Chemical species
  • Polar snow

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

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