4.3 Article

Soluble, light-absorbing species in snow at Barrow, Alaska

Journal

Publisher

AMER GEOPHYSICAL UNION
DOI: 10.1029/2011JD016181

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Funding

  1. NSF [ATM-0807702]
  2. French Polar Institute
  3. IPEV [1017-OASIS]
  4. Directorate For Geosciences [0807702] Funding Source: National Science Foundation
  5. Directorate For Geosciences
  6. Office of Polar Programs (OPP) [0806437] Funding Source: National Science Foundation
  7. Div Atmospheric & Geospace Sciences [0807702] Funding Source: National Science Foundation

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As part of the international multidisciplinary Ocean - Atmosphere - Sea Ice - Snowpack (OASIS) program we analyzed more than 500 terrestrial (melted) snow samples near Barrow, AK between February and April 2009 for light absorption, as well as H2O2 and inorganic anion concentrations. For light absorption in the photochemically active region (300-450 nm) of surface snows, H2O2 and NO3- make minor contributions (combined < 9% typically), while HUmic LIke Substances (HULIS) and unknown chromophores each account for approximately half of the total absorption. We have identified four main sources for our residual chromophores (i.e., species other than H-2(2)O or NO3-): (1) vegetation and organic debris impact mostly the lowest 20 cm of the snowpack, (2) marine inputs, which are identified by high Cl- and SO42- contents, (3) deposition of diamond dust to surface snow, and (4) gas-phase exchange between the atmosphere and surface snow layers. The snow surfaces, and accompanying chromophore concentrations, are strongly modulated by winds and snowfall at Barrow. However, even with these physical controls on light absorption, we see an overall decline of light absorption in near-surface snow during the 7 weeks of our campaign, likely due to photo-bleaching of chromophores. While HULIS and unknown chromophores dominate light absorption by soluble species in Barrow snow, we know little about the photochemistry of these species, and thus we as a community are probably overlooking many snowpack photochemical reactions.

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