首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Dissolved and particulate Fe in a hydrothermal plume at 9 degrees 45 ' N, East Pacific Rise: Slow Fe (II) oxidation kinetics in Pacific plumes
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Dissolved and particulate Fe in a hydrothermal plume at 9 degrees 45 ' N, East Pacific Rise: Slow Fe (II) oxidation kinetics in Pacific plumes

机译:东太平洋上升9°45'N的热液羽流中溶解的颗粒状Fe:太平洋羽流中缓慢的Fe(II)氧化动力学

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Production of Fe(III) particles in hydrothermal plumes is of fundamental importance to the long-term effect of hydrothermal circulation on seawater composition. To elucidate the fundamental controls on Fe redox kinetics and solution/particle partitioning in neutrally buoyant plumes, we sampled near-field (<3 km) plume particles at 9 degrees 45'N on the East Pacific Rise in 1996, returning in 1997 to sample both particulate and dissolved phases (0.40 mu m filter). Concentrations of dissolved Fe varied from 320 to 20 nM in proximal (<0.3 km from vent site) to distal samples (1-3 km downfield), constituting similar to 85-50% of total Fe, respectively. Based on vent fluid dilution factors calculated from dissolved Mn, a mass balance for vent fluid Fe at this site indicates that similar to 65% of Fe is lost to particulate sulfide settling in the buoyant plume, and that particulate Fe in distal (1-3 km) samples is twice as concentrated as predicted from dilution of particles in proximal plume water. These observations are consistent with a calculated Fe(II) oxidation half-time of 3.3 h, long enough that Fe(III) colloid production and aggregation occurs primarily in the neutrally buoyant plume at relatively high dilutions, preventing generation of high particulate Fe concentrations (11-56 nM observed). A general investigation of Fe(II) oxidation rates in plumes worldwide gives Fe(II) oxidation half-lives as short as 17 min at some Atlantic sites, and as long as 6 h at some Pacific sites. The calculations indicate that the distribution of Fe particles in plumes depends chiefly on inter-basin differences in ambient deep water chemistry (primarily pH and dissolved O-2) and on local currents driving plume dilution, and to a much lesser extent on variations in primary vent fluid composition. Long-term changes in thermohaline circulation or ocean biogeochemistry may therefore alter Fe dynamics and minor element fluxes associated with global hydrothermal activity, independent of variations in crustal production rates. Copyright (C) 1999 Elsevier Science Ltd. [References: 53]
机译:热液羽流中Fe(III)颗粒的产生对于热液循环对海水成分的长期影响至关重要。为了阐明对中性浮羽中铁氧化还原动力学和溶液/颗粒分配的基本控制,我们于1996年在东太平洋上升沿9度45'N采样近场(<3 km)羽状颗粒,1997年返回采样颗粒相和溶解相(0.40微米过滤器)。溶解的铁浓度在近端(距通风口<0.3 km)至远端样品(低场1-3 km)的范围为320至20 nM,分别占总铁的85%至50%。根据从溶解的Mn计算得出的排气液稀释系数,此位置的排气液Fe的质量平衡表明,漂浮在浮羽中的颗粒硫化物沉降损失了大约65%的Fe,而远端的颗粒Fe则损失了(1-3 km)样品的浓度是近端羽状水中颗粒稀释所预测浓度的两倍。这些观察结果与计算得出的Fe(II)氧化半衰期为3.3小时是一致的,时间足够长,以至于Fe(III)胶体的产生和聚集主要发生在相对较高稀释度的中性浮力羽流中,从而阻止了高颗粒Fe浓度的产生(观察到11-56 nM)。对世界范围内烟羽中Fe(II)氧化速率的一般研究表明,在某些大西洋地区,Fe(II)氧化半衰期短至17分钟,而在某些太平洋地区则长达6小时。计算表明,烟羽中铁颗粒的分布主要取决于环境深水化学中的流域间差异(主要是pH和溶解的O-2)以及驱动烟羽稀释的局部电流,在较小程度上取决于烟羽中Fe的分布。排气液成分。因此,热盐循环或海洋生物地球化学的长期变化可能会改变铁的动力学和与全球热液活动有关的微量元素通量,而与地壳生产率的变化无关。版权所有(C)1999 Elsevier Science Ltd. [引用:53]

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