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首页> 外文期刊>Atmospheric chemistry and physics >Airborne mercury species at the Rao background monitoring site in Sweden: distribution of mercury as an effect of long-range transport
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Airborne mercury species at the Rao background monitoring site in Sweden: distribution of mercury as an effect of long-range transport

机译:瑞典Rao背景监测点的空气中汞物种:汞的分布作为远程运输的影响

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Within the EU-funded project, Global Mercury Observation System (GMOS) airborne mercury has been monitored at the background Rao measurement site on the western coast of Sweden from mid-May 2012 to the beginning of July 2013 and from the beginning of February 2014 to the end of May 2015. The following mercury species/fractions were measured: gaseous elemental mercury (GEM), particulate bound mercury (PBM) and gaseous oxidised mercury (GOM) using the Tekran measurement system. The mercury concentrations measured at the Rao site were found to be low in comparison to other, comparable, European measurement sites. A back-trajectory analysis to study the origin of air masses reaching the Rao site was performed. Due to the remote location of the Rao measurement station it receives background air about 60% of the time. However, elevated mercury concentrations arriving with air masses coming from the south-east are noticeable. GEM and PBM concentrations show a clear annual variation with the highest values occurring during winter, whereas the highest concentrations of GOM were obtained in spring and summer. An evaluation of the diurnal pattern of GOM, with peak concentrations at midday or in the early afternoon, which often is observed at remote places, shows that it is likely to be driven by local meteorology in a similar way to ozone. Evidence that a significant part of the GOM measured at the Rao site has been formed in free tropospheric air is presented.
机译:在欧盟资助的项目中,从2012年5月中旬至2013年7月初,以及从2014年2月初至2013年7月,在瑞典西海岸的Rao背景测量场对全球汞观测系统(GMOS)的空气中汞进行了监测。截止到2015年5月。使用Tekran测量系统测量了以下汞种类/馏分:气态元素汞(GEM),颗粒结合汞(PBM)和气态氧化汞(GOM)。与其他可比较的欧洲测量站点相比,在饶站点测量的汞浓度较低。进行了向后轨迹分析,以研究到达Rao站点的气团的起源。由于Rao测量站位于遥远的地方,因此它大约有60%的时间接收背景空气。但是,值得注意的是,东南方向的空气团导致汞浓度升高。 GEM和PBM浓度显示出明显的年度变化,最高值出现在冬季,而GOM最高值出现在春季和夏季。对GOM的昼夜模式进行评估后,通常会在偏远地区观察到中午或午后的峰值浓度,这表明它很可能是由当地气象学驱动的,类似于臭氧。提出的证据表明在对流层自由空气中形成了在饶地点测得的GOM的很大一部分。

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