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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Long-term, continuous OsmoSampler results for interstitial waters from an active gas venting site at a shallow gas hydrate field, Umitaka Spur, eastern margin of the Japan Sea
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Long-term, continuous OsmoSampler results for interstitial waters from an active gas venting site at a shallow gas hydrate field, Umitaka Spur, eastern margin of the Japan Sea

机译:长期,连续的Osmosampler为来自浅天然气水合物领域的活性气体通风位点,乌塔卡卡刺,日本海域东部边缘

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Highly active gas venting and outcrops of gas hydrates were recently found at the Umitaka Spur, on the eastern margin of the Japan Sea, through seafloor observations using a remotely operated vehicle (ROV). This was followed by sampling by using conventional coring techniques. In this study, we deployed a long-term osmotic fluid sampling system (OsmoSampler) to record geochemical changes in the shallow sedimentary environment over time. The OsmoSampler collected interstitial water at 30 cm below seafloor (cmbsf), providing us with a continuous daily record of the concentrations of SO42-, Cl-, CH4, and C2H6 dissolved in interstitial waters over one year. General mean concentrations of SO42- and Cl- repeatedly showed synchronous increases and decreases over both long-term (i.e. dozens of days) and short-term (i.e. 3-5 days) periods. Such fluctuations relative to background seawater concentrations were likely caused by saline and fresh water generation due to gas hydrate formation and dissolution. The CH4 concentration was significantly higher (> 1 mM) during large fluctuations in SO42- and Cl- over the first 3 months, which was attributable to gas-venting activity. This high venting activity of CH4 could have promoted the rapid, large-scale formation of gas hydrate. The CH4 concentration decreased gradually after the first 3 months, and was accompanied by a period of relatively low SO42- and Cl- concentrations due to the predominance of gas hydrate dissolution around the sampling site. In later months, the C2H6 concentration approached similar to 1 mu M and was accompanied by occasional, positive CH4 spikes, reflecting the release of trapped gases associated with the dissolution of hydrates. These processes are essentially controlled by the fluctuations in gas concentrations along the gas migration path, and are well-characterized by shallow interstitial water geochemistry.
机译:最近在日本海域东部边缘的乌塔卡卡·斯普尔(Rov)的海底观测中发现了高活性气体水合物的气体水合物露头。通过使用传统的芯技术进行采样。在这项研究中,我们部署了长期渗透流体采样系统(Osmosampler),以记录浅沉积环境随时间的地球化学变化。 Osmosampler在海底(CMBSF)以下30厘米处收集了间质水,为我们提供了一年多的SO42,CL-,CH4和C2H6浓度的连续日常记录。 SO42-和CL-反复显示同步增加并减少长期(即数十天)和短期(即3-5天)期间的同步增加和减少。由于天然气水合物形成和溶解,盐水和淡水产生的这种波动可能是由盐水和淡水引起的。在SO42-和CL-在前3个月内大波动期间,CH 4浓度明显高于(> 1mm),其可归因于膨胀活性。这种高通风活性CH4可以促进迅速,大规模的天然气水合物形成。在前3个月后,CH 4浓度逐渐降低,并且由于气体水合物溶解在取样部位周围的主要偏移而伴随着相对低的SO42-和CL-浓度的时期。在以后的几个月中,接近的C2H6浓度与1μm相似,并伴随偶尔的阳性CH4尖峰,反映了与水合物溶解相关的捕获气体的释放。这些方法基本上由沿气体迁移路径的气体浓度的波动来控制,并且通过浅层间水地球化学进行了良好的特征。

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