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全新世以来气候驱动的有机结合态铀向高山湖泊的通量。

Climate-driven fluxes of organic-bound uranium to an alpine lake over the Holocene.

机构信息

Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie (IMPMC), UMR 7590, Sorbonne Université-CNRS-MNHN-IRD, Paris, France.

Univ Savoie Mont Blanc, CNRS, Edytem, UMR 5204, Chambéry, France.

出版信息

Sci Total Environ. 2021 Aug 20;783:146878. doi: 10.1016/j.scitotenv.2021.146878. Epub 2021 Apr 1.

Abstract

Uranium (U) isotopic signatures and concentration in sediments are widely used as paleo-redox proxies, as the behavior of U is often controlled by bottom water oxygenation. Here, we investigated the processes controlling U accumulation in the sediments of Lake Nègre (Mediterranean Alps, South-East France) over the past 9200 years. Exceptionally high natural U concentrations (350-1250 μg·g) allowed the measurement of U along with other elements by high-resolution X-Ray Fluorescence core-scanning. Weathering and erosion proxies (Ti content, Zr/Al and K/Ti ratios) indicate that sedimentary inputs were controlled by Holocene climatic variations. After a period of low erosion during the Holocene Climatic Optimum, a major regime shift was recorded at 4.2 kyr BP when terrigenous fluxes consistently increased until present with high sensitivity to centennial-scale climatic events. Sedimentary organic matter (OM) inputs were dominated by terrigenous OM from the catchment soils until 2.4 kyr BP, as attested by carbon to nitrogen (C/N) and bromine to organic carbon (Br/TOC) ratios. From 2.4 kyr BP to present, lake primary production and soils equally contributed to sedimentary OM. Uranium fluxes to the sediments were well correlated to terrigenous OM fluxes from 7 kyr BP to present, showing that U supply to the lake was controlled by U scavenging in the soils of the watershed followed by transport of U bound to detrital organic particles. Higher U/OM ratios before 7 kyr BP likely reflect the development of the upstream wetland. The fluctuations of U sedimentary inputs appear to be independent of bottom water oxygenation, as estimated from constant Fe/Mn ratios and δU isotopic signatures, and rather controlled by the production, erosion and sedimentation of terrigenous OM. This finding confirms that the use of U (and potentially other metals with high affinity to OM) concentrations alone should be used with caution for paleo-redox reconstructions.

摘要

铀(U)同位素特征和浓度广泛用于古氧化还原指标,因为 U 的行为通常受底层水氧合作用控制。在这里,我们研究了过去 9200 年来控制法国东南部地中海阿尔卑斯山内格勒湖沉积物中 U 积累的过程。异常高的天然 U 浓度(350-1250μg·g)允许通过高分辨率 X 射线荧光核心扫描测量 U 以及其他元素。风化和侵蚀指标(Ti 含量、Zr/Al 和 K/Ti 比值)表明,沉积输入受全新世气候变化控制。在全新世气候最优期经历了一段低侵蚀期后,在 4.2 千年前记录到了一个主要的制度转变,当时陆源通量持续增加,直到现在,对百年尺度的气候事件高度敏感。沉积有机质(OM)输入主要由流域土壤中的陆源 OM 控制,直到 2.4 千年前,这可以通过碳氮比(C/N)和溴有机碳比(Br/TOC)来证明。从 2.4 千年前到现在,湖泊初级生产力和土壤同样为沉积 OM 做出了贡献。U 通量与 7 千年前至今的陆源 OM 通量呈很好的相关性,表明 U 向湖泊的供应受流域土壤中 U 捕获的控制,随后 U 与碎屑有机颗粒结合并运输。7 千年前之前 U/OM 比值较高,可能反映了上游湿地的发展。U 沉积物输入的波动似乎与底层水氧合作用无关,这可以从恒定的 Fe/Mn 比值和 δU 同位素特征来估计,而是受陆源 OM 的产生、侵蚀和沉积控制。这一发现证实,仅使用 U(和可能其他与 OM 亲和力高的金属)浓度来进行古氧化还原重建时应谨慎使用。

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