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Depositional control on carbon and sulfur preservation onshore and offshore the Oujiang Estuary: Implications for the C/S ratio as a salinity indicator

机译:川芎和海上川芎的沉积控制瓯江河口:对C / S比例的影响为盐度指示器

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Carbon and sulfur preserved in estuary and shelf sediments play a critical role in controlling sediment diagenesis related to the global biogeochemical cycle. Their ratio (C/S = 2.8) in mud sediments has been widely used to distinguish freshwater from marine environments; however, this ratio can be influenced by depositional evolution, physical reworking, and other sedimen-tological parameters. We present a new C/S ratio data set from surface sediments of five rivers (Aojiang, Feiyunjiang, Jiaojiang, Oujiang, and Qiantangjiang Rivers), as well as core sediments offshore of the Oujiang Estuary (core EC2005, 60 m), to discuss how the evolution of the depositional environment influenced carbon and sulfur preservation since the last degradation. To this aim, we measured the contents of total organic carbon (TOC), total sulfur (TS), and carbonate in the collected samples. Our results demonstrate that a C/S ratio of 2.8 can effectively separate freshwater environments (river sediments and core sediments deposited before 13.1 ka), suggesting the initial impact of sulfate-enriched seawater on carbon and sulfur perseveration at ~13.1 ka. However, the TS content is independent of the TOC content after 13.1 ka, implying that pyrite sulfur is derived not only from organoclastic sulfate reduction (OSR) but also from sul-fate-driven anaerobic oxidation of methane (AOM) under anoxic diagenetic conditions. In the shallowest core section (shallower than 5 m; < 1.5 ka), the C/S ratios gradually increase from 1 to 2.8, which corresponds to an interval with sulfide reoxidation under suboxic conditions caused by strong physical reworking. When the sediment is buried to a certain depth (deeper than 5 m; > 1.5 ka), a high sedimentation rate is conducive to an AOM reaction, resulting in the generation of a large amount of pyrite and finally causing the minimum value of the C/S ratio to be approximately 1. However, during the transitional period of 13.1-11.0 ka, sediments deposited in the tidal environment show overlap with those deposited in the marine shelf environment, and C/S ratios decrease from >10 to ~1. In addition, we propose that C/S and C/N ratios could be combined to reveal the depositional evolution from terrestrial to marine environments, which is sensitive to sea level and climatic changes. Therefore, our new findings suggest that the sedimentation process can modulate the diagenetic path of mud sediments (e.g., OSR versus AOM), and geochemical indicators of environmental evolution should be carefully used in combination with sedimentological parameters in shallow depositional environments.
机译:在河口和架子沉积物中保存的碳和硫在控制与全球生物地球化学循环相关的沉积物成岩作用方面发挥着关键作用。它们在泥浆沉积物中的比例(C / S = 2.8)已被广泛用于区分淡水从海洋环境;然而,这种比率可以受到沉积演化,物理垫料和其他沉泥语言参数的影响。我们提出了一种新的C / S比例,从五条河流(Aojiang,Feiyunjiang,Jiaojiang,Oujiang和Ciantangjiang Rivers)以及欧江河口的核心沉积物(核心EC2005,60米)的核心沉积物,讨论自上次退化以来,沉积环境的演变如何影响碳和硫保存。为此,我们测量了收集样品中总有机碳(TOC),总硫(TS)和碳酸盐的含量。我们的结果表明,2.8的C / S比可以有效地将淡水环境(河流沉积物和核沉积物沉积在13.1 ka之前)分开,表明富含硫酸盐的海水对〜13.1ka的碳和硫的持久性初步影响。然而,TS含量与13.1ka后的TOC含量无关,暗示硫铁矿硫的硫酸盐还原(OSR)衍生,而且在缺氧作用条件下也来自甲烷(AOM)的甲烷(AOM)的硫酸厌氧氧化。在最浅的核心部分(浅比5米; <1.5 ka)中,C / S比率从1〜2.8逐渐增加,这对应于由强大的物理重新加工引起的中草氧化条件下的硫化物再氧化的间隔。当沉积物被埋到一定的深度时(比5米更深),高沉降率有利于AOM反应,导致大量的黄铁矿并最终导致C的最小值。 / S比率约为1。然而,在13.1-11.0ka的过渡期间,潮汐环境中沉积的沉积物显示与沉积在船舶架子环境中的那些,C / S比减少> 10至〜1。此外,我们提出C / S和C / N比可以组合以揭示从陆地到海洋环境的沉积演进,这对海平面和气候变化很敏感。因此,我们的新发现表明,沉降过程可以调节泥浆沉积物的成岩路径(例如,OSR与AOM),并且应在浅层沉积环境中与沉积学参数结合仔细使用环境进化的地球化学指标。

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  • 来源
    《Oceanographic Literature Review》 |2021年第9期|1929-1929|共1页
  • 作者

    X. Liu; M. Zhang; A. Li;

  • 作者单位

    Key Laboratory of Submarine Geosciences and Prospecting Technology College of Marine Geosciences Ocean University of China Qingdao 266100 China;

    Key Laboratory of Submarine Geosciences and Prospecting Technology College of Marine Geosciences Ocean University of China Qingdao 266100 China;

    Key Laboratory of Submarine Geosciences and Prospecting Technology College of Marine Geosciences Ocean University of China Qingdao 266100 China;

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