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Preservation of organic matter in marine sediments by inner-sphere interactions with reactive iron

机译:内球与反应性铁的相互作用保护海洋沉积物中的有机物

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摘要

Interactions between organic matter and mineral matrices are critical to the preservation of soil and sediment organic matter. In addition to clay minerals, Fe(III) oxides particles have recently been shown to be responsible for the protection and burial of a large fraction of sedimentary organic carbon (OC). Through a combination of synchrotron X-ray techniques and high-resolution images of intact sediment particles, we assessed the mechanism of interaction between OC and iron, as well as the composition of organic matter co-localized with ferric iron. We present scanning transmission x-ray microscopy images at the Fe L3 and C K1 edges showing that the organic matter co-localized with Fe(III) consists primarily of C=C, C=O and C-OH functional groups. Coupling the co-localization results to iron K-edge X-ray absorption spectroscopy fitting results allowed to quantify the relative contribution of OC-complexed Fe to the total sediment iron and reactive iron pools, showing that 25–62% of total reactive iron is directly associated to OC through inner-sphere complexation in coastal sediments, as much as four times more than in low OC deep sea sediments. Direct inner-sphere complexation between OC and iron oxides (Fe-O-C) is responsible for transferring a large quantity of reduced OC to the sedimentary sink, which could otherwise be oxidized back to CO2.
机译:有机物与矿物基质之间的相互作用对于保护土壤和沉积物有机物至关重要。除粘土矿物外,最近还显示出Fe(III)氧化物颗粒可用于保护和掩埋大部分沉积有机碳(OC)。通过同步加速器X射线技术和完整沉积物颗粒的高分辨率图像的结合,我们评估了OC和铁之间的相互作用机理,以及与三价铁共定位的有机物的组成。我们目前在Fe L3和C K1边缘呈现扫描透射X射线显微镜图像,表明与Fe(III)共存的有机物主要由C = C,C = O和C-OH官能团组成。将共定位结果与铁的K边缘X射线吸收光谱拟合结果耦合,可以量化OC复合铁对总沉积铁和活性铁池的相对贡献,表明总活性铁的25–62%为通过沿海沉积物中的内圈络合作用与OC直接相关,是低OC深海沉积物中的四倍。 OC和氧化铁(Fe-O-C)之间的直接内球络合负责将大量还原的OC转移到沉积池中,否则它们可能被氧化回CO2。

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