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Rates of organic carbon oxidation in deep sea sediments in the eastern North Atlantic from pore water profiles of O_2 and the Delta~(13)C of dissolved inorganic carbon

机译:从O_2的孔隙水剖面和溶解的无机碳的Delta〜(13)C剖面看北大西洋东部深海沉积物中有机碳的氧化速率

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摘要

The remineralization rate of sedimentary organic carbon (R+(org)) and the depth-integrated, diffusion-supplied O_2 consumption rate (IOC) during microbial metabolism in sediments was investigated in three deep-sea sites at 1100, 2000 and 3500 m water depth in the eastern north Atlantic during the spring and summer 1998. In-situ pore water O_2 profiles yielded an IOC of 0.45 + - 0.07 mmol O_2 m~(-2) day~(-1) at the deepest site (n=3) and ca. 1-1.5 mmol O_2 m~(-2) day~(-1) at the shallowest site (n=2). The Rare was independently estimated at all three sites from ex-situ pore water profiles of the isotopic composition of total dissolved inorganic carbon (delta~(13)Cr), assuming that the concentration and isotopic composition of pore water Cr with depth in the sediment was controlled only by microbial oxidation of isotopically depleted sedimentary organic carbon. The R_(org) was thus estimated to be ca. 0.5-0.6 mmol C m~(-2) day~(-1) at the shallowest site and ca. 0.3-0.4 mmol C m~(-2) day~(-1) at the two deeper sites. Stoichiometric and isotopic constraints indicated that oxic remineralization of sedimentary organic matter was the dominant metabolic pathway in the sediments at 3500 m water depth. Similarly, Stoichiometric and isotopic constraints suggested that the R_(org) estimates from the ex-situ pore water delta~(13)Cr profiles from 1100 and 2000 m water depth were likely to be minimum values and provided evidence for the occurrence of post-oxic remineralization processes. Post-oxic metabolism in the sediments of these sites could be linked to, or even augmented by, the non-diffusive mode of supply of organic matter mediated by infaunal organisms below the oxic sediment layer.
机译:在1100、2000和3500 m水深的三个深海地点,研究了沉积物微生物代谢过程中沉积物有机碳的再矿化率(R +(org))和深度综合,扩散提供的O_2消耗率(IOC)。 1998年春季和夏季,在北大西洋东部。原位孔隙水O_2剖面在最深处(n = 3)产生的IOC为0.45 +-0.07 mmol O_2 m〜(-2)天〜(-1)。和。最浅处(n = 2)为1-1.5 mmol O_2 m〜(-2)天〜(-1)。假设沉积物中孔隙水Cr的浓度和同位素组成随沉积物深度而变,则根据溶解的总无机碳(δ〜(13)Cr)的同位素组成的异位孔隙水剖面独立地估计这三个位置的稀有度只能通过同位素消耗的沉积有机碳的微生物氧化来控制。因此估计R_(org)为约。 0.5-0.6 mmol C m〜(-2)天〜(-1)最浅处和在两个较深的位置处0.3-0.4 mmol C m〜(-2)天〜(-1)。化学计量和同位素约束表明,沉积有机质的有氧再矿化作用是水深3500 m的沉积物中主要的代谢途径。同样,化学计量学和同位素约束表明,从1100和2000 m水深处的异位孔隙水δ〜(13)Cr剖面得出的R_(org)估计值可能是最小值,并提供了发生后地震的证据。有氧再矿化过程。这些位点沉积物中的有氧后新陈代谢可能与有氧沉积层以下的臭名昭著的生物体介导的有机物的非扩散供应方式有关,甚至有所增加。

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