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1.
Artigo em Inglês | MEDLINE | ID: mdl-31534978

RESUMO

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.

2.
J Geophys Res Oceans ; 120(12): 7699-7721, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27812435

RESUMO

Each year, the arctic sea ice edge retreats from its winter maximum extent through the Seasonal Ice Zone (SIZ) to its summer minimum extent. On some days, this retreat happens at a rapid pace, while on other days, parts of the pan-arctic ice edge hardly move for periods of days up to 1.5 weeks. We term this stationary behavior "ice edge loitering," and identify areas that are more prone to loitering than others. Generally, about 20-25% of the SIZ area experiences loitering, most often only one time at any one location during the retreat season, but sometimes two or more times. The main mechanism controlling loitering is an interaction between surface winds and warm sea surface temperatures in areas from which the ice has already retreated. When retreat happens early enough to allow atmospheric warming of this open water, winds that force ice floes into this water cause melting. Thus, while individual ice floes are moving, the ice edge as a whole appears to loiter. The time scale of loitering is then naturally tied to the synoptic time scale of wind forcing. Perhaps surprisingly, the area of loitering in the arctic seas has not changed over the past 25 years, even as the SIZ area has grown. This is because rapid ice retreat happens most commonly late in the summer, when atmospheric warming of open water is weak. We speculate that loitering may have profound effects on both physical and biological conditions at the ice edge during the retreat season.

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