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通过与反应性铁的内球相互作用来保存海洋沉积物中的有机物。

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

机构信息

GEOTOP and the Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke West, Montréal, Quebec, H4B 1R6, Canada.

Skidaway Institute of Oceanography, University of Georgia, 10 Ocean Science Circle, Savannah, GA, 31411, USA.

出版信息

Sci Rep. 2017 Mar 23;7(1):366. doi: 10.1038/s41598-017-00494-0.

DOI:10.1038/s41598-017-00494-0
PMID:28336935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5428421/
Abstract

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 L and C K 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 CO.

摘要

有机质与矿物基质之间的相互作用对于土壤和沉积物有机质的保存至关重要。除了粘土矿物外,最近的研究表明,三价铁氧化物颗粒对于保护和埋藏大部分沉积有机碳(OC)也起到了至关重要的作用。通过同步辐射 X 射线技术和完整沉积物颗粒的高分辨率图像相结合,我们评估了 OC 与铁之间相互作用的机制,以及与三价铁共定位的有机质的组成。我们展示了在 Fe L 和 C K 边缘的扫描透射 X 射线显微镜图像,表明与 Fe(III)共定位的有机质主要由 C=C、C=O 和 C-OH 官能团组成。将共定位结果与铁 K 边 X 射线吸收光谱拟合结果相结合,使我们能够定量确定 OC 结合铁对总沉积物铁和反应性铁库的相对贡献,结果表明,在沿海沉积物中,有 25-62%的总反应性铁直接通过内圈络合与 OC 相关,这一比例是低 OC 深海沉积物的四倍之多。OC 与氧化铁(Fe-O-C)之间的直接内圈络合作用将大量还原态 OC 转移到沉积物汇中,否则这些 OC 可能会被氧化回 CO。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/c4601a4f94b0/41598_2017_494_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/1786e49f58f9/41598_2017_494_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/cb4274624625/41598_2017_494_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/58bdd72ac08d/41598_2017_494_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/7415a458c3c5/41598_2017_494_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/1acb65b226de/41598_2017_494_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/c4601a4f94b0/41598_2017_494_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/1786e49f58f9/41598_2017_494_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/cb4274624625/41598_2017_494_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/58bdd72ac08d/41598_2017_494_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/7415a458c3c5/41598_2017_494_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/1acb65b226de/41598_2017_494_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/5428421/c4601a4f94b0/41598_2017_494_Fig6_HTML.jpg

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