U.S. Army Cold Regions Research & Engineering Laboratory , PO Box 35170, Fort Wainwright, Alaska 99703, United States.
Geophysical Institute University of Alaska Fairbanks , Fairbanks, Alaska 99775, United States.
Environ Sci Technol. 2017 Oct 3;51(19):11145-11155. doi: 10.1021/acs.est.7b03683. Epub 2017 Sep 20.
Atmospheric mercury (Hg) is deposited to Polar Regions during springtime atmospheric mercury depletion events (AMDEs) that require halogens and snow or ice surfaces. The fate of this Hg during and following snowmelt is largely unknown. We measured Hg, major ions, and stable water isotopes from the snowpack through the entire spring melt runoff period for two years. Our small (2.5 ha) watershed is near Barrow (now Utqiaġvik), Alaska. We measured discharge, made 10 000 snow depths, and collected over 100 samples of snow and meltwater for chemical analysis in 2008 and 2009 from the watershed snowpack and ephemeral stream channel. Results show an "ionic pulse" of mercury and major ions in runoff during both snowmelt seasons, but major ion and Hg runoff concentrations were roughly 50% higher in 2008 than in 2009. Though total discharge as a percent of total watershed snowpack water equivalent prior to the melt was similar in both years (36% in 2008 melt runoff and 34% in 2009), it is possible that record low precipitation in the summer of 2007 led to the higher major ion and Hg concentrations in 2008 melt runoff. Total dissolved Hg meltwater runoff of 14.3 (± 0.7) mg/ha in 2008 and 8.1 (± 0.4) mg/ha in 2009 is five to seven times higher than that reported from other arctic watersheds. We calculate 78% of snowpack Hg was exported with snowmelt runoff in 2008 and 41% in 2009. Our results suggest AMDE Hg complexed with Cl or Br may be less likely to be photochemically reduced and re-emitted to the atmosphere prior to snowmelt, and we estimate that roughly 25% of the Hg in snowmelt is attributable to AMDEs. Projected Arctic warming, with more open sea ice leads providing halogen sources that promote AMDEs, may provide enhanced Hg deposition, reduced Hg emission and, ultimately, an increase in snowpack and snowmelt runoff Hg concentrations.
大气汞(Hg)在春季大气汞消耗事件(AMDEs)期间被沉积到极地,该事件需要卤素和雪或冰面。在融雪期间和之后,这种 Hg 的命运在很大程度上是未知的。我们在两年内测量了雪层中的 Hg、主要离子和稳定的水同位素。我们的小流域(2.5 公顷)位于阿拉斯加的巴罗(现名为 Utqiaġvik)附近。我们测量了排放量,测量了 10000 次雪深,并在 2008 年和 2009 年从流域积雪和短暂的溪流中采集了超过 100 个雪和融水样本进行化学分析。结果表明,在两个融雪季节,径流中都存在 Hg 和主要离子的“离子脉冲”,但 2008 年的主要离子和 Hg 径流浓度比 2009 年高约 50%。尽管在融雪之前,总排放量占总流域积雪水当量的比例在两年内相似(2008 年融雪径流为 36%,2009 年为 34%),但 2007 年夏季创纪录的低降雨量可能导致 2008 年融雪径流中主要离子和 Hg 浓度升高。2008 年总溶解 Hg 融水径流量为 14.3(±0.7)mg/ha,2009 年为 8.1(±0.4)mg/ha,是其他北极流域报告值的五到七倍。我们计算出,2008 年有 78%的积雪 Hg 随融雪径流排出,2009 年为 41%。我们的结果表明,与 Cl 或 Br 络合的 AMDE Hg 可能不太可能在融雪之前通过光化学还原和重新排放到大气中,我们估计,融雪中约有 25%的 Hg 归因于 AMDEs。预计北极变暖,开阔的海冰提供促进 AMDEs 的卤素源,可能会增加 Hg 的沉积,减少 Hg 的排放,并最终增加积雪和融雪径流 Hg 浓度。