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Elevated uranium concentrations in Lake Baikal sediments: Burial and early diagenesis

机译:贝加尔湖沉积物中铀浓度升高:埋藏和早期成岩作用

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The water column of Lake Baikal (Siberia) is pervasively oxic and O-2 penetrates several cm into the sediment, followed by distinct layers of Fe/Mn oxide that undergo reductive-dissolution/oxidative-precipitation cycles. Uranium (U) contents of the oxic surface sediment layers were similar to 15 mu g g(-1), which is unparalleled in oxygenated lakes. To understand the processes leading to this enrichment we investigated the geochemical composition of the particulate matter and pore water of four sediment cores from different locations in the lake and performed mass balance calculations based on sediment mass accumulation rates and published loads from major tributaries. The comparison of loads and export of U in Lake Baikal suggested that current estimates of loads are too low by a factor of about 3 compared to sediment mass accumulation rates. Peak loads during spring ice melt in tributaries that are difficult to monitor and quantify might be the main cause for the deviation. The high U concentrations in the lake sediments originated from the scavenging of U in the water column through association with settling organic particles and particulate Fe(III)- and, to a lesser extent, Mn(IV)-oxides. We outline the hypothesis that two distinct U phases, lithogenic and non-lithogenic U reach the lake sediment and that authigenic U is subsequently formed under reducing conditions within the sediment. In some cores we found that most U was remobilized during the degradation of organic matter, in particular within the top oxygenated layer of the sediment. Significant enrichments prevailed due to U adsorption to and/or co-precipitation with Fe-oxides. When Fe-oxides and, to a lesser extent, Mn-oxides were reductively dissolved, they released U to the pore water, leading to peak dissolved U concentrations in the anoxic sediment, which in turn, precipitated as authigenic U under predominantly sulphate-reducing conditions. The onset of the accumulation of authigenic U coincided with the formation of distinct Fe/Mn oxide layers above. We argue that the resilience of Fe-oxides (especially crystalline goethite and hematite), in association with phosphate, even within reducing (but non-sulfidic) sediments support the burial of substantial amounts of U. (C) 2016 Elsevier B.V. All rights reserved.
机译:贝加尔湖(西伯利亚)的水柱普遍是含氧的,O-2渗透到沉积物中几厘米,然后是经过还原-溶解/氧化-沉淀循环的Fe / Mn氧化物不同层。含氧表面沉积物层中的铀(U)含量类似于15μg g(-1),这在含氧湖中是无与伦比的。为了了解导致富集的过程,我们研究了湖中不同位置的四个沉积物核心的颗粒物和孔隙水的地球化学组成,并根据沉积物质量累积速率和主要支流公布的负荷进行了质量平衡计算。贝加尔湖中铀的负荷和出口的比较表明,与沉积物质量积累速率相比,目前对负荷的估计太低了约3倍。支流中春季冰融化过程中的峰值载荷难以监控和量化,可能是造成偏差的主要原因。湖泊沉积物中高浓度的U源自水柱中U的清除,这是通过与沉降的有机颗粒和颗粒Fe(III)-以及较小程度的Mn(IV)-氧化物结合而产生的。我们概述了一个假设,即两个截然不同的U相,即成岩性U相和非非成岩性U相到达湖泊沉积物,然后在沉积物内部还原条件下形成了自生U质。在某些岩心中,我们发现大多数U在有机物降解期间被迁移,特别是在沉积物的顶部氧化层内。由于U吸附到Fe-氧化物上和/或与Fe-氧化物共沉淀,所以大量富集盛行。当氧化铁和氧化锰(在较小程度上)被还原溶解时,它们将U释放到孔隙水中,导致缺氧沉积物中溶解的U浓度达到峰值,进而在主要减少硫酸盐的情况下沉淀为自生U。条件。自生铀的积累开始与上面独特的Fe / Mn氧化物层的形成相吻合。我们认为,即使在还原(但非硫化)沉积物中,Fe-氧化物(特别是结晶针铁矿和赤铁矿)与磷酸盐的回弹力也支持大量铀的埋葬。(C)2016 Elsevier BV版权所有。

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