首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Reverse weathering in marine sediments and the geochemical cycle of potassium in seawater: Insights from the K isotopic composition ( 41K/ 39K) of deep-sea pore-fluids
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Reverse weathering in marine sediments and the geochemical cycle of potassium in seawater: Insights from the K isotopic composition ( 41K/ 39K) of deep-sea pore-fluids

机译:海洋沉积物中的逆转风化和海水中钾的地球化学循环:来自K同位素组成的见解( 41 k / 深海孔隙液的39 k)

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In situ Al-silicate formation, also known as “reverse weathering,” is an important sink of many of the major and minor cations in seawater (e.g. Mg, K, and Li). However, the importance of this sink in global geochemical cycles and isotopic budgets of these elements remains poorly constrained. Here, we report on the potassium isotopic composition (41K/39K) of deep-sea sediment pore-fluids from four (Integrated) Ocean Drilling Program sites (1052, U1378, U1395 and U1403) to characterize potassium isotopic fractionation associated with the formation of authigenic Al-silicate minerals in marine sediments and its role in elevating the41K/39K of seawater relative to bulk silicate Earth. Isotopic ratios are obtained by high-resolution multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) in cold plasma conditions with a long-term external reproducibility of ca. 0.17‰. We find that, although all sites are characterized by pore-fluid K concentrations that decline with increasing depth, their K isotopic profiles vary systematically from site-to-site; at sites characterized by rapid sedimentation rates, pore-fluid profiles of41K/39K are relatively invariant whereas at sites characterized by slow sedimentation rates,41K/39K declines with depth by up to 1.8‰. Results from 1-D diffusion-advection-reaction models suggest that these differences may result from a complex interplay between sedimentation rate and fractionation of K isotopes during diffusion, Al-silicate authigenesis, and ion exchange. Model simulations suggest fractionation factors between 0.9980 and 1.0000 for reverse weathering reactions in deep-sea sediments. Although deep-sea sites do not constitute major sinks of K in seawater, some of the processes responsible for K isotopic fractionation at these sites (diffusion and Al-silicate authigenesis) likely play a role in determining the41K/39K of seawater.
机译:原位Al-硅酸盐形成,也称为“反向风化”,是海水中许多主要和小阳离子的重要汇(例如Mg,K和Li)。然而,这种汇在全球地球化学循环和这些元素的同位素预算中的重要性仍然受到严重的限制。在这里,我们报告了来自四(综合)海洋钻井计划网站(1052,U1378,U1395和U1403)的深海沉积物孔流体的钾同位素组合物(41K / 39K),以表征与形成相关的同位素分级海洋沉积物中的AtheAgenic Al-硅酸盐矿物质及其在升高41K / 39K相对于散装硅酸盐地球的作用。同位素比率通过高分辨率的多集聚器电感耦合等离子体质谱(MC-ICP-MS)在冷等离子体条件下,具有CA的长期外部再现性。 0.17‰。我们发现,尽管所有网站的特征在于孔隙流体K浓度,其随着深度的增加而下降,但它们的K同位素谱系从现场系统地变化;在特征在于快速沉淀速率的遗址,41K / 39K的孔隙流体型材相对不变,而在沉淀速率缓慢表征的场地,41K / 39K深度下降至1.8‰。 1-D扩散 - 平面反应模型的结果表明,这些差异可能是由于扩散,硅酸盐作家和离子交换期间K同位素的沉积速率和分馏之间的复杂相互作用而导致。模型模拟建议在深海沉积物中逆转风化反应的0.9980和1.0000之间的分馏因素。虽然深海地点不构成海水中K的主要汇,但是在这些位点(扩散和Al-硅酸盐作家的分数)负责K同位素分级的一些过程可能在确定41K / 39K海水中起作用。

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