Dept. of Chemistry "Ugo Schiff", University of Florence, Via della Lastruccia, 3, 50019 Sesto F.no (Florence), Italy.
DISAT-University Milano-Bicocca, Piazza della Scienza, 1, 20126 Milano, Italy; University of Siena, Earth Science Department, Via Laterino, 8, 53100 Siena, Italy.
Chemosphere. 2017 Jun;176:273-287. doi: 10.1016/j.chemosphere.2017.02.115. Epub 2017 Mar 16.
In this work we present the isotopic, chemical and dust stratigraphies of two snow pits sampled in 2013/14 at GV7 (coastal East Antarctica: 70°41' S - 158°51' E, 1950 m a.s.l.). A large number of chemical species are measured aiming to study their potentiality as environmental changes markers. Seasonal cluster backward trajectories analysis was performed and compared with chemical marker stratigraphies. Sea spray aerosol is delivered to the sampling site together with snow precipitation especially in autumn-winter by air masses arising from Western Pacific Ocean sector. Dust show maximum concentration in spring when the air masses arising from Ross Sea sector mobilize mineral dust from ice-free areas of the Transantarctic mountains. The clear seasonal pattern of sulfur oxidized compounds allows the dating of the snow-pit and the calculation of the mean accumulation rate, which is 242 ± 71 mm w.e. for the period 2008-2013. Methanesulfonic acid and NO do not show any concentration decreasing trend as depth increases, also considering a 12 m firn core record. Therefore these two compounds are not affected by post-depositional processes at this site and can be considered reliable markers for past environmental changes reconstruction. The rBC snow-pit record shows the highest values in summer 2012 likely related to large biomass burning even occurred in Australia in this summer. The undisturbed accumulation rate for this site is demonstrated by the agreement between the chemical stratigraphies and the annual accumulation rate of the two snow-pits analysed in Italian and Korean laboratories.
本工作介绍了 2013/14 年在 GV7(东南极海岸:70°41'S-158°51'E,海拔 1950 米)采集的两个雪坑的同位素、化学和尘埃地层学。测量了大量化学物质,旨在研究它们作为环境变化标志物的潜力。进行了季节性聚类轨迹向后分析,并与化学标记地层学进行了比较。特别是在秋季至冬季,来自西太平洋海域的气团将海雾气溶胶与雪降水一起输送到采样点。当来自罗斯海海域的气团将来自南极山脉无冰区的矿物质尘埃迁移时,尘埃在春季达到最高浓度。硫氧化化合物的明显季节性模式允许对雪坑进行定年,并计算平均积累率,该时期(2008-2013 年)的平均积累率为 242±71mm w.e.。甲磺酸和 NO 没有表现出任何随深度增加而降低的浓度趋势,同时还考虑了 12 米的冰芯记录。因此,这两种化合物不受该地点的沉积后过程影响,可以被认为是过去环境变化重建的可靠标志物。rBC 雪坑记录在 2012 年夏季达到最高值,可能与当年夏季澳大利亚发生的大规模生物质燃烧有关。意大利和韩国实验室分析的两个雪坑的化学地层学和年积累率之间的一致性证明了该地点未受干扰的积累率。