{"title":"Chemical constituents in the air and snow at Dye 3, Greenland—II. Analysis of episodes in April 1989","authors":"C.I. Davidson , J.-L. Jaffrezo , B.W. Mosher , J.E. Dibb , R.D. Borys , B.A. Bodhaine , R.A. Rasmussen , C.F. Boutron , F.M. Ducroz , M. Cachier , J. Ducret , J.-L. Collin , N.Z. Heidam , K. Kemp , R. Hillamos","doi":"10.1016/0960-1686(93)90305-I","DOIUrl":null,"url":null,"abstract":"<div><p>Detailed examination of a two-week period in April 1989 during the Dye 3 Gas and Aerosol Sampling Program shows that episodes of relatively high concentration of certain chemical constituents occur at this time of year. Airborne concentrations of crustal metals such as Al and Ca can exceed 100 ng m<sup>−3</sup>, while concentrations of SO<sub>4</sub><sup>2−</sup> can exceed 1000 ng m<sup>−3</sup>. Elevated concentrations of MSA, <sup>7</sup>Be and <sup>210</sup>Pb are also noted. Consideration of synoptic maps and backward air mass trajectories suggests that the episodes are due to transport from a variety of source regions, including Eurasia (transport over the Pole), North America and western Europe. In addition to elevated airborne concentrations, levels of these constituents in surface snow are high during April. However, it is difficult to develop quantitative relationships between concentrations in air and in snow due to the difficulty in measuring airborne concentrations at cloud-level; variations in scavenging by clouds may also be significant. It is concluded that the springtime maxima in airborne concentrations resulting from long-range transport from a variety of source regions are responsible for strong identifiable signals in ice cores and snowpits from this region.</p></div>","PeriodicalId":100139,"journal":{"name":"Atmospheric Environment. Part A. General Topics","volume":"27 17","pages":"Pages 2723-2737"},"PeriodicalIF":0.0000,"publicationDate":"1993-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0960-1686(93)90305-I","citationCount":"41","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Environment. Part A. General Topics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/096016869390305I","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 41
Abstract
Detailed examination of a two-week period in April 1989 during the Dye 3 Gas and Aerosol Sampling Program shows that episodes of relatively high concentration of certain chemical constituents occur at this time of year. Airborne concentrations of crustal metals such as Al and Ca can exceed 100 ng m−3, while concentrations of SO42− can exceed 1000 ng m−3. Elevated concentrations of MSA, 7Be and 210Pb are also noted. Consideration of synoptic maps and backward air mass trajectories suggests that the episodes are due to transport from a variety of source regions, including Eurasia (transport over the Pole), North America and western Europe. In addition to elevated airborne concentrations, levels of these constituents in surface snow are high during April. However, it is difficult to develop quantitative relationships between concentrations in air and in snow due to the difficulty in measuring airborne concentrations at cloud-level; variations in scavenging by clouds may also be significant. It is concluded that the springtime maxima in airborne concentrations resulting from long-range transport from a variety of source regions are responsible for strong identifiable signals in ice cores and snowpits from this region.
1989年4月染料3号气体和气溶胶取样计划期间的两个星期的详细检查表明,每年的这个时候都会出现某些化学成分浓度相对较高的情况。空气中地壳金属如Al和Ca的浓度可超过100 ng m−3,而SO42−的浓度可超过1000 ng m−3。MSA、7Be和210Pb的浓度也有所升高。对天气图和向后的气团轨迹的考虑表明,这些事件是由于来自各种来源区域的输送,包括欧亚大陆(极地上空的输送)、北美和西欧。除了空气中这些成分的浓度升高外,4月份地表雪中这些成分的含量也很高。然而,由于难以测量云水平的空气浓度,因此很难建立空气中浓度和雪中的浓度之间的定量关系;云清除的变化也可能很重要。由此得出结论,来自不同源区的远距离输送造成的空气中浓度的春季最大值是该地区冰芯和雪坑的强烈可识别信号的原因。