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Fractionation of silicon isotopes during biogenic silica dissolution

机译:生物硅溶解过程中硅同位素的分馏

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Silicon isotopes have been investigated for their potential to reveal both past and present patterns of silicic acid utilization,primarily by diatoms, in surface waters of the ocean. Interpretation of this proxy has thus far relied on characteristic trends in the isotope composition of the dissolved and particulate silicon pools in the upper ocean, as driven by biological fractionation during the production of biogenic silica (bSiO2, or opal) by diatoms. However, other factors which may influence the silicon isotope composition of diatom opal, particularly post-formational aging and maturation processes, remain largely uninvestigated.Here, we report a consistent fractionation of silicon isotopes during the physicochemical dissolution of diatom bSiO2 suspended in seawater under closed conditions. This fractionation acts counter to that occurring during bSiO2 production and at about half its absolute magnitude, with dissolution discriminating against the release of the heavier isotopes of silicon at an enrichment factor eDSi–BSi of 0.55&, corresponding to a fractionation factor a30/28 of 0.99945. The enrichment factor did not vary with source material, indicating the lack of a significant species effect, or with temperature from 3 to 20 C. Thus, the dissolution of bSiO2 produces dissolved silicon with a d30Si value that is 0.55& more negative than its parent bSiO2, an effect that must be accounted for when interpreting oceanic d30Si distributions. The d30Si values of both the dissolved and particulate silicon pools increased linearly as dissolution progressed, implying a measurable (±0.1&) change in the relative d30Si of opal samples whenever the difference in preservation efficiency between them is >20%. This effect could account for 10–30% of the difference in diatom d30Si values observed between glacial and interglacial conditions. It is unlikely, however, that the inferred maximum possible change in db30SiO2 of +0.55& would be manifested in situ, as a high mean percentage of dissolution would include complete loss of the more soluble members of the diatom assemblage.
机译:已经研究了硅同位素的潜力,这些潜力揭示了海洋表层水中硅酸利用的过去和现在的模式,主要是硅藻。迄今为止,对这种替代物的解释一直依赖于上层海洋中溶解和颗粒状硅池的同位素组成的特征趋势,这是由硅藻生产生物硅(bSiO2或蛋白石)过程中的生物分级分离所驱动的。然而,其他可能影响硅藻蛋白硅同位素组成的因素(尤其是形成后的老化和成熟过程)尚未得到充分研究。条件。这种分馏作用与bSiO2生产过程中发生的分馏作用相反,并且大约是其绝对量的一半,其溶出作用可区分出以0.55&的富集因子eDSi-BSi释放较重的硅同位素,相当于分馏因子a30 / 28。 0.99945。富集因子没有随原料变化,表明没有明显的物种效应,也没有随温度在3至20 C之间变化。因此,bSiO2的溶解会产生溶解的硅,其d30Si值比其母体多0.55或更大。 bSiO2,一种在解释海洋d30Si分布时必须考虑的效应。随着溶解的进行,溶解态硅颗粒池和颗粒态硅池的d30Si值均呈线性增加,这意味着蛋白石样品的相对d30Si相对于保存效率的差异> 20%时,可测量的变化为(±0.1&)。这种影响可能解释了冰川和冰川间条件下观察到的硅藻d30Si值差异的10%至30%。但是,不可能推断出db30SiO2的最大可能变化为+ 0.55&,因为较高的平均溶解百分率将完全损失硅藻组合物中较易溶的成员。

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