Abstract

Abstract. Gaseous elemental mercury (GEM) was monitored at the Niwot Ridge (NWT) Long-Term Ecological Research (LTER) site (Colorado, USA, 40° N) from interstitial air extracted from the snowpack at depths ranging from the snow surface to 10 cm above the soil. A highly dynamic cycling of mercury (Hg) in this mid-latitude snowpack was observed. Patterns were driven by both GEM production in surface snow and GEM destruction in the deeper snowpack layers. Thorough mixing and vertical transport processes were observed through the snowpack. GEM was photochemically produced near the snow-air interface throughout the entire winter, leading to enhanced GEM levels in interstitial air of surface snow of up to 8 ng m−3. During low-wind periods, GEM in surface snow layers remained significantly above ambient air levels at night as well, which may indicate a potential weak GEM production overnight. Analyses of vertical GEM gradients in the snowpack show that surface GEM enhancements efficiently propagated down the snowpack, with a temporal lag in peak GEM levels observed with increasing depth. Downward diffusion was responsible for much of these patterns, although vertical advection also contributed to vertical redistribution. Destruction of GEM in the lower snowpack layers was attributed to dark oxidation of GEM. Analysis of vertical GEM / CO2 flux ratios indicated that this GEM destruction occurred in the snow and not in the underlying soil. The strong, diurnal patterns of photochemical GEM production at the surface ultimately lead to re-emission losses of deposited Hg back to the atmosphere. The NWT data show that highest GEM surface production and re-emissions occur shortly after fresh snowfall, which possibly resupplies photoreducible Hg to the snowpack, and that photochemical GEM reduction is not radiation-limited as it is strong even on cloudy days.

Highlights

  • All Gaseous elemental mercury (GEM) data collected in snow interstitial air (SIA) and discussed in this study were combined to evenly spaced 30 cm depth intervals down from the top of the snowpack; e.g., the 0–30 cm layer contains data when inlets were sampling at that depth range; in the same way we summarized all other depth layers

  • This representation of data is different from previous publications resulting from the Niwot Ridge (NWT) snow tower (Williams et al, 2009, and references therein) but is appropriate for GEM, a reactive gas experiencing fast production processes in the upper layer of the snowpack

  • Corresponding CO2 mixing ratios were approximately 389 ppm in ambient air, which increased with depth to peak mixing ratios of 3390 ppm in the lowest snowpack layer (i.e., 150–180 cm depth). This example demonstrates the performance and reliability of the measurements; for example, the CO2 mixing ratio gradient follows patterns that have been well characterized for this alpine snowpack (Liptzin et al, 2009, and references therein); very similar GEM and CO2 snowpack profiles were seen during the 2011–2012 winter season where similar measurements were conducted

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Summary

Objectives

The main goals of this study were to improve our understanding of Hg(II)/GEM redox conversions within the snowpack and to assess how such conversions affect Hg loads of alpine snowpacks during snowpack accumulation and snowmelt

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Results
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