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Atmospheric sulphur and cloud condensation nuclei in marine air in the Southern Hemisphere

机译:南半球海洋空气中的大气硫和云凝结核

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摘要

Measurements of atmospheric sulphur species made in Southern Ocean air, at the Cape Grim Baseline Air Pollution Station, are reviewed in an attempt to discern the role played by oceanic emissions of dimethyl sulphide (DMS) as a source of cloud condensation nuclei (CCN). Consistent with conclusions reached by others, our data indicate that the connection between DMS concentration and CCN concentration is neither simple nor direct, being mediated through a range of chemical pathways and intermediate species that are subject to considerable variability over timescales ranging from minutes to months. Physical and meteorological processes are no less important than chemical processes as sources of complexity in the DMS to CCN transformation process. Moreover, the considerable uncertainty that currently exists about both the number of chemical pathways involved in DMS oxidation, and the kinetic coefficients associated with the proposed pathways, make quantitative modelling studies problematic. Nevertheless, synthesis of a large body of data available from Cape Grim and other Southern Ocean sites does permit some refinement of our understanding of the DMS–CCN connection. Here, these data are employed to illustrate the current state of knowledge about the connections between DMS, CCN and cloud properties at Cape Grim, and to highlight the many complexities that underlie these connections.
机译:审查了在海角格里姆基线空气污染站对南部海洋空气中的大气硫物质进行的测量,以期确定海洋排放的二甲基硫(DMS)作为云凝结核(CCN)的来源所起的作用。与其他人得出的结论一致,我们的数据表明DMS浓度和CCN浓度之间的联系既不简单也不直接,是通过一系列化学途径和中间物种介导的,这些化学途径和中间物种在数分钟至数月的时间范围内会发生较大变化。作为DMS到CCN转换过程中复杂性的来源,物理和气象过程与化学过程同样重要。此外,目前有关DMS氧化的化学途径数量以及与拟议途径相关的动力学系数都存在相当大的不确定性,这使得定量建模研究成为问题。尽管如此,从格里姆角和其他南大洋站点获得的大量数据的综合确实使我们对DMS-CCN连接的理解有了一些改进。在这里,这些数据被用来说明有关Cape Grim的DMS,CCN和云属性之间联系的当前知识状态,并强调这些联系背后的许多复杂性。

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