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铁锰增强的长期有机碳封存

Long-term organic carbon preservation enhanced by iron and manganese.

机构信息

School of Earth and Environment, University of Leeds, Leeds, UK.

School of Geography, University of Leeds, Leeds, UK.

出版信息

Nature. 2023 Sep;621(7978):312-317. doi: 10.1038/s41586-023-06325-9. Epub 2023 Aug 2.

DOI:10.1038/s41586-023-06325-9
PMID:37532941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10499600/
Abstract

The balance between degradation and preservation of sedimentary organic carbon (OC) is important for global carbon and oxygen cycles. The relative importance of different mechanisms and environmental conditions contributing to marine sedimentary OC preservation, however, remains unclear. Simple organic molecules can be geopolymerized into recalcitrant forms by means of the Maillard reaction, although reaction kinetics at marine sedimentary temperatures are thought to be slow. More recent work in terrestrial systems suggests that the reaction can be catalysed by manganese minerals, but the potential for the promotion of geopolymerized OC formation at marine sedimentary temperatures is uncertain. Here we present incubation experiments and find that iron and manganese ions and minerals abiotically catalyse the Maillard reaction by up to two orders of magnitude at temperatures relevant to continental margins where most preservation occurs. Furthermore, the chemical signature of the reaction products closely resembles dissolved and total OC found in continental margin sediments globally. With the aid of a pore-water model, we estimate that iron- and manganese-catalysed transformation of simple organic molecules into complex macromolecules might generate on the order of approximately 4.1 Tg C yr for preservation in marine sediments. In the context of perhaps only about 63 Tg C yr variation in sedimentary organic preservation over the past 300 million years, we propose that variable iron and manganese inputs to the ocean could exert a substantial but hitherto unexplored impact on global OC preservation over geological time.

摘要

沉积物有机碳(OC)的降解和保存之间的平衡对全球碳氧循环很重要。然而,促进海洋沉积物 OC 保存的不同机制和环境条件的相对重要性仍不清楚。简单的有机分子可以通过美拉德反应聚合成难降解的形式,尽管在海洋沉积物温度下的反应动力学被认为是缓慢的。最近在陆地系统中的研究表明,该反应可以被锰矿物催化,但在海洋沉积物温度下促进聚硅酸 OC 形成的潜力尚不确定。在这里,我们进行了孵育实验,发现铁和锰离子和矿物在与大陆边缘相关的温度下,通过非生物催化作用,将美拉德反应提高了两个数量级,而大陆边缘是大多数保存发生的地方。此外,反应产物的化学特征与全球大陆边缘沉积物中发现的溶解态和总 OC 非常相似。借助孔隙水模型,我们估计,简单有机分子在铁和锰催化作用下转化为复杂的大分子,可能会在海洋沉积物中产生约 4.1 Tg C yr 的保存量。在过去 300 百万年中,沉积物有机碳保存量可能只有约 63 Tg C yr 的变化,我们提出,海洋中铁和锰的输入量变化可能会对地质时间内的全球 OC 保存产生实质性但迄今尚未被探索的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/94aad50c46ed/41586_2023_6325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/b559b25108ba/41586_2023_6325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/69dfbd06882c/41586_2023_6325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/94aad50c46ed/41586_2023_6325_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/b559b25108ba/41586_2023_6325_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/69dfbd06882c/41586_2023_6325_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/628d/10499600/94aad50c46ed/41586_2023_6325_Fig3_HTML.jpg

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