首页> 外文期刊>Atmospheric chemistry and physics >Circumpolar transport and air-surface exchange of atmospheric mercury at Ny-Ålesund (79° N), Svalbard, spring 2002
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Circumpolar transport and air-surface exchange of atmospheric mercury at Ny-Ålesund (79° N), Svalbard, spring 2002

机译:Ny-Å lesund(79° N)的大气汞的绕极传输和空气表面交换,斯瓦尔巴群岛,2002春季

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Mercury in different environmental compartments has been measured atNy-Ålesund (78°54' N, 11°53' E) during an intensive campaign,17 April to 14 May 2002. Time-resolved speciated determination of mercuryin the atmosphere and snow was conducted at the Norwegian research stationat the Zeppelin mountain, 474 m above the sea level, and at the Italianresearch facility Dirigibile Italia, 12 m above the sea level. Total GaseousMercury (TGM) was present in the range <0.1 to 2.2 ng m−3 during thecampaign. Three mercury depletion events, identified as periods withdecreased TGM concentrations, were observed. At the lower altitude, TGMconcentrations following such events were found to exhibit both highermagnitude and larger variability in comparison to results from the Zeppelinstation. Oxidised mercury species in air and fall-out with snow as well asmercury attached to particles were also measured and their concentrationswere found to be anti-correlated with TGM in air. concentrations of total Hg in snow (Hg-tot)showed a large (~15×) increase in response to Gaseous Elemental Mercury Depletion Events (GEMDEs, range 1.5–76.5 ng L−1).Solid evidence for photo-stimulated emissions ofHg0(g) from the snow pack in conjunction to depletion events wereobtained from gradient measurements as well as from flux chambermeasurements. Steep diurnal concentration variations of Hg0(aq) insurface seawater were also found to concur with changing solar radiation.The concentration of Hg0(aq) in seawater was found to be in the range12.2–70.4 pg L−1, which corresponds to supersaturation. Hence, theseawater surface constituted a source emitting elemental mercury.The concentrations of RGM (reactive gaseous mercury), Hg-p (particulatemercury), and BrO column densities (detected by DOAS) were very low exceptfor a few individual samples during the major Hg0 depletion event. BrO vertical columndensities obtained by the remote satellite ESR-2 and trajectory analysis indicate thatthe air masses exhibiting low Hg0 concentrations originated from areas with high BrOdensities.
机译:在2002年4月17日至5月14日的一次密集运动中,在Ny-Ålesund(北纬78°54'N,西经11°53')处测量了不同环境隔室中的汞。挪威研究站位于齐柏林峰山,海拔474 m,意大利研究机构Dirigibile Italia,海拔12 m。在活动期间,总气态汞(TGM)的范围为<0.1至2.2 ng m -3 。观察到三个汞消耗事件,这被确定为TGM浓度降低的时期。与Zeppelinstation的结果相比,在较低的高度,发现此类事件后的TGM浓度显示出更高的幅度和更大的变异性。还测量了空气中的氧化汞物种以及因雪而降落的雪以及附着在颗粒上的汞,并且发现它们的浓度与空气中的TGM反相关。对气态元素汞消耗事件(GEMDE,范围为1.5-76.5 ng L −1 )的响应,雪中总Hg浓度(Hg-tot)显示出较大的变化(〜15倍)。通过梯度测量和通量室测量获得了雪堆中光激发的Hg 0 (g)的排放以及耗尽事件。还发现表层海水中Hg 0 (aq)的急剧日浓度变化与太阳辐射的变化同时发生;发现海水中Hg 0 (aq)的浓度为在12.2–70.4 pg L -1 范围内,这对应于过饱和。因此,海水表面构成了排放元素汞的源.RGM(反应性气态汞),Hg-p(微粒汞)和BrO柱密度(由DOAS检测)的浓度非常低,除了在主要Hg < sup> 0 耗竭事件。遥测卫星ESR-2的BrO垂直柱密度和轨迹分析表明,Hg 0 浓度低的空气质量源于BrO浓度高的地区。

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