Seasonal aerosol chemistry at Dye 3, Greenland

Byard W. Mosher, P. Winkler, Jean-Luc Jaffrezo
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引用次数: 68

Abstract

Aerosol trace element concentrations spanning an eleven month period at Dye 3, Greenland are presented. Sea salt input into the lower atmosphere of the ice sheet occurs predominantly in the winter months of December-February. These aerosols are the product of vigorous Arctic winter storms. Long range transport of crustal material from lower latitude arid regions to the Greenland Ice Sheet takes place predominantly during the spring. The onset of Arctic sunrise and associated weakening of the surface and upper level inversion over the ice sheet appear to be important factors resulting in higher crustal aerosol concentrations in the lower levels of the Greenland atmosphere during the month of April. A strong pulse of crustal aerosol (260 ng Al scm−1) was observed at Dye 3 on 14–15 April 1989. Meteorological evidence suggests that strong winds and deep convective activity injected dust high into the atmosphere over the Sahara desert region. This airmass then appears to have passed northwand over western Europe where it mixed with anthropogenic aerosols and arrived in the Dye 3 region some 4–6 d hence. Elevated concentrations of anthropogenic aerosol species were also observed at the surface during the months of April and May. Long range transport of these aerosols appears to be important during the Arctic winter and spring, while enhanced downward mixing due to a weakening inversion results in elevated concentrations at the surface during April and May. An increase in scavenging due to persistent Arctic stratus and the northward migration of the Polar Front in the spring results in very low anthropogenic aerosol concentrations during the summer months. Particulate aerosol iodine and bromine concentrations also peak during the month of April at Dye 3. It has been suggested that this spring particulate halogen peak, which is observed throughout the Arctic, may be the result of photochemical aerosol production from biogenic organo-halogen species. Regional meteorological phenomena as well as seasonal variations in source strength and long range transport appear to be important factors influencing aerosol concentrations in the surface atmosphere of the Greenland Ice Sheet.

格陵兰岛Dye 3的季节性气溶胶化学
气溶胶微量元素浓度跨越11个月期间在染料3,格陵兰提出。海盐输入到冰盖低层大气主要发生在冬季的12月至2月。这些气溶胶是北极冬季强烈风暴的产物。地壳物质从低纬度干旱地区向格陵兰冰盖的长距离运输主要发生在春季。北极日出的开始以及与之相关的冰盖表面和高层逆温的减弱似乎是导致4月份格陵兰岛低层大气中地壳气溶胶浓度升高的重要因素。1989年4月14-15日,在第3号染区观测到强烈的地壳气溶胶脉冲(260 ng Al scm−1)。气象证据表明,强风和深层对流活动将沙尘注入撒哈拉沙漠地区的高空大气。然后这个气团似乎向北经过西欧,在那里它与人为气溶胶混合,并在大约4-6天后到达Dye 3地区。在4月和5月期间,在地表观测到人为气溶胶种类的浓度升高。这些气溶胶的远距离输送在北极冬季和春季似乎很重要,而由于逆温减弱而增强的向下混合导致4月和5月地面浓度升高。由于持续的北极层云和春季极锋的北移,清除量的增加导致夏季几个月的人为气溶胶浓度非常低。颗粒气溶胶碘和溴浓度也在4月份在第3区达到峰值。有人认为,整个北极地区观测到的这个春季微粒卤素峰值可能是由生物源有机卤素物种产生的光化学气溶胶的结果。区域气象现象以及源强度和远距离输送的季节变化似乎是影响格陵兰冰盖表面大气气溶胶浓度的重要因素。
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