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An investigation of the origins of reactive gaseous mercury in the Mediterranean marine boundary layer

机译:地中海船舶边界层反应性气态汞的起源研究

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Atmospheric mercury species concentrations were measured during two oceanographic cruise campaigns covering the Adriatic Sea, the first during the autumn in 2004 and the second in the summer of 2005. The inclement weather during the autumn campaign meant that no clear in-situ production of oxidised gas phase mercury was seen. Events where high values of HgII(g) and/or Hg associated with particulates (HgP) were observed, could be linked to probable anthropogenic emission source areas. During the summer campaign however, the by now rather familiar diurnal variation of HgII(g) concentration, with maxima around midday, was observed. Again there were events when high HgII(g) and particulates (HgP) concentrations were seen which did not fit with the pattern of daily in-situ HgII(g) production. These events were traceable, with the help of back trajectory calculations, to areas of anthropogenic emissions. The back trajectories for all the events during which high Hg species concentrations were encountered showed that the airmass being sampled had passed near port areas in the previous 24 h. Not all these ports are associated with major industrial installations, it is possible therefore (bearing in mind the uncertainty associated with the back trajectory calculations) that either shipping or port activities are a Hg source. Box modelling studies of the summer 2005 campaign show that although the in-situ production of HgII(g) occurs in the MBL, the exact chemical mechanism responsible is difficult to determine. However given the high O3 concentrations encountered during this campaign it seems clear that if Hg0 does react with O3, it does not produce gas phase HgII. Equally, the reaction between Hg0 and OH if it occurs, does not contribute appreciably to HgII(g) production.
机译:在覆盖亚得里亚海的两个海洋巡航活动期间测量了大气汞种浓度,于2004年秋季,第二届在2005年夏天的第二次。秋季运动期间的恶劣天气意味着没有明确的原位生产氧化气体看到阶段汞。观察到与颗粒(HGP)相关的HGII(g)和/或Hg的高值的事件可以与可能的人为发射源区域连接。然而,在夏季运动期间,观察到目前常见的HGII(g)浓度的差异,午间中午的最大程度的变化。再次出现了高HGII(G)和颗粒(HGP)浓度的情况,其不适合日常原位HGII(G)生产的模式。这些事件可追溯到后轨迹计算,对人为排放区域。遇到高HG物种浓度的所有事件的后轨迹表明,在前24小时的港口区域中采样近港口区域。并非所有这些端口都与主要工业安装相关联,因此可以(铭记与后轨道计算相关的不确定性),运输或港口活动是HG源。 2005年夏季框展示研究表明,尽管在MBL中发生HGII(G)的原位产生,但难以确定的确切化学机制。然而,考虑到在这一运动期间遇到的高O3浓度似乎很明显,如果HG0确实与O 3反应,则它不会产生气相HGII。同样地,HG0和OH之间的反应如果发生,并且不会与HGII(G)的产生明显贡献。

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