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Snowpack measurements suggest role for multi-year sea ice regions in Arctic atmospheric bromine and chlorine chemistry.
Peterson, Peter K; Hartwig, Mark; May, Nathaniel W; Schwartz, Evan; Rigor, Ignatius; Ermold, Wendy; Steele, Michael; Morison, James H; Nghiem, Son V; Pratt, Kerri A.
Afiliação
  • Peterson PK; Department of Chemistry, University of Michigan, Ann Arbor, Michigan, US.
  • Hartwig M; Now at Department of Chemistry, Whittier College, Whittier, California, US.
  • May NW; Department of Chemistry, University of Michigan, Ann Arbor, Michigan, US.
  • Schwartz E; Department of Chemistry, University of Michigan, Ann Arbor, Michigan, US.
  • Rigor I; Department of Chemistry, University of Michigan, Ann Arbor, Michigan, US.
  • Ermold W; Now at Department of Molecular Biosciences, University of Texas, Austin, Texas, US.
  • Steele M; Applied Physics Laboratory, University of Washington, Seattle, Washington, US.
  • Morison JH; Applied Physics Laboratory, University of Washington, Seattle, Washington, US.
  • Nghiem SV; Applied Physics Laboratory, University of Washington, Seattle, Washington, US.
  • Pratt KA; Applied Physics Laboratory, University of Washington, Seattle, Washington, US.
Article em En | MEDLINE | ID: mdl-31534978
ABSTRACT
As sources of reactive halogens, snowpacks in sea ice regions control the oxidative capacity of the Arctic atmosphere. However, measurements of snowpack halide concentrations remain sparse, particularly in the high Arctic, limiting our understanding of and ability to parameterize snowpack participation in tropospheric halogen chemistry. To address this gap, we measured concentrations of chloride, bromide, and sodium in snow samples collected during polar spring above remote multi-year sea ice (MYI) and first-year sea ice (FYI) north of Greenland and Alaska, as well as in the central Arctic, and compared these measurements to a larger dataset collected in the Alaskan coastal Arctic by Krnavek et al. (2012). Regardless of sea ice region, these surface snow samples generally featured lower salinities, compared to coastal snow. Surface snow in FYI regions was typically enriched in bromide and chloride compared to seawater, indicating snowpack deposition of bromine and chlorine-containing trace gases and an ability of the snowpack to participate further in bromine and chlorine activation processes. In contrast, surface snow in MYI regions was more often depleted in bromide, indicating it served as a source of bromine-containing trace gases to the atmosphere prior to sampling. Measurements at various snow depths indicate that the deposition of sea salt aerosols and halogen-containing trace gases to the snowpack surface played a larger role in determining surface snow halide concentrations compared to upward brine migration from sea ice. Calculated enrichment factors for bromide and chloride, relative to sodium, in the MYI snow samples suggests that MYI regions, in addition to FYI regions, have the potential to play an active role in Arctic boundary layer bromine and chlorine chemistry. The ability of MYI regions to participate in springtime atmospheric halogen chemistry should be considered in regional modeling of halogen activation and interpretation of satellite-based tropospheric bromine monoxide column measurements.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Elementa (Wash D C) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Elementa (Wash D C) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos
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