Chemical constituents in the air and snow at Dye 3, Greenland—I. Seasonal variations

C.I. Davidson , J.-L. Jaffrezo , B.W. Mosher , J.E. Dibb , R.D. Borys , B.A. Bodhaine , R.A. Rasmussen , C.F. Boutron , U. Gorlach , H. Cachier , J. Ducret , J.-L. Colin , N.Z. Heidam , K. Kemp , R. Hillamo
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引用次数: 81

Abstract

Chemical constituent concentrations in air and snow from the Dye 3 Gas and Aerosol Sampling Program show distinct seasonal patterns. These patterns are different from those observed at sea-level sites throughout the Arctic. Airborne SO42− and several trace metals ofcrustal and anthropogenic origin show strong peaks in the spring, mostly in April. Some species also have secondary maxima in the fall. The spring peaks are attributed to transport over the Pole from Eurasian sources, as well as transport from eastern North America and western Europe. The fall peaks are attributed primarily to transport from North America, and less frequent transport from Europe. Airborne 7Be and 210Pb show strong peaks in both spring and fall, suggesting that vertical atmospheric mixing is favored during these two seasons. Several other airborne constituents peak at other times. For example, Na peaks in winter due to transport of seaspray from storms in ice-free oceanic areas, while MSA peaks in summer due to biogenic production in the oceans nearby. Many trace gases such as freons and other chlorine-containing species show roughly uniform concentrations throughout the year. CO and CH4 show weak peaks in February–March. Concentrations of chemical constituents in fresh snow at Dye 3 also show distinct seasonal patterns. SO42− and several trace metals show springtime maxima, consistent with the aerosol data. Na shows a winter maximum and MSA shows a summer maximum in the snow, also consistent with the aerosols. 7Be and 210Pb in the snow do not show any strong variation with season. Similarly, soot and total carbon in snow do not show strong variation. When used with dry deposition models, these air and snow concentration data suggest that dry deposition of submicron aerosol species has relatively minor influence on constituent levels in the snowpack at Dye 3 compared to wet deposition inputs (including scavenging by fog); crustal aerosol, on the other hand, may have a more significant input by dry deposition. Overall, the results suggest that gross seasonal patterns of some aerosol species are constistent in the air and in fresh snow, although individual episodes in the air are not always reflected in the snow. The differences in data reported here compared with data sets for sea-level arctic sites demonstrate the need for sampling programs on the Ice Sheet in order to properly interpret Greenland glacial record data.

格陵兰岛三号染料区空气和雪中的化学成分。季节性的变化
染料3气体和气溶胶取样计划中空气和雪中的化学成分浓度显示出明显的季节性模式。这些模式不同于在整个北极海平面观测到的模式。空气中SO42−和几种地壳和人为来源的微量金属在春季出现强烈的峰值,主要在4月份。一些物种在秋季也有二次最大值。春季的高峰归因于来自欧亚大陆的运输,以及来自北美东部和西欧的运输。秋季的高峰主要归因于来自北美的运输,以及来自欧洲的运输频率较低。大气中7Be和210Pb在春季和秋季均表现出较强的峰值,表明这两个季节有利于大气垂直混合。其他几种空气成分在其他时间达到峰值。例如,Na在冬季达到峰值是由于无冰海域风暴带来的海粉的运输,而MSA在夏季达到峰值是由于附近海洋的生物生产。许多微量气体,如氟利昂和其他含氯气体,全年的浓度大致相同。CO和CH4在2 - 3月呈弱峰值。染料3号新雪中化学成分的浓度也显示出明显的季节性模式。SO42−和几种微量金属显示春季最大值,与气溶胶资料一致。Na显示冬季最大值,MSA显示夏季最大值,也与气溶胶一致。积雪中be和210Pb的季节变化不明显。同样,雪中烟灰和总碳的变化也不明显。当与干沉降模式一起使用时,这些空气和雪浓度数据表明,与湿沉降输入(包括雾的清除)相比,亚微米气溶胶种类的干沉降对染料3区积雪成分水平的影响相对较小;另一方面,地壳气溶胶可能有更重要的干沉积输入。总的来说,结果表明,尽管空气中的个别事件并不总是反映在雪中,但某些气溶胶物种在空气和新鲜雪中的总体季节性模式是一致的。这里报告的数据与海平面北极地点的数据集的差异表明,为了正确解释格陵兰冰川记录数据,需要在冰盖上进行采样程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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