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首页> 外文期刊>American Journal of Science >THE WEATHERING OF SEDIMENTARY ORGANIC MATTER AS A CONTROL ON ATMOSPHERIC O_2: I. ANALYSIS OF A BLACK SHALE
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THE WEATHERING OF SEDIMENTARY ORGANIC MATTER AS A CONTROL ON ATMOSPHERIC O_2: I. ANALYSIS OF A BLACK SHALE

机译:沉积有机物的风化作为大气O_2的控制:I.黑色页岩的分析

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摘要

To investigate the weathering of sedimentary organic matter and its role in regulating atmospheric oxygen, a drill core of black shale from the New Albany formation (Upper Devonian, Clay City, KY) has been analyzed for total and organic carbon, nitrogen, phosphorus, and sulfur and for porosity, permeability and specific surface area. The distribution of organic matter and pyrite in the shale has also been examined by means of electron photomicrography and element mapping. Element mapping indicates that shale organic matter is present mainly as 0.5 to 50 mu m discoidal clots and discontinuous laminae ("stringers") and not as monomolecular coatings on clay grains. Loss of organic matter by oxidative weathering takes place across a reaction "front" where organic carbon content decreases sharply toward the land surface along with organic nitrogen and sulfur, but not organic phosphorus which remains relatively constant over the same depth range. Accompanying the decrease in organic matter is an increase in porosity. These results agree with earlier work on a single stratigraphic layer that found also that the oxygen content of the organic matter increases sharply toward the land surface across a similar carbon oxidation front. Pyrite in both the core and the layer was found to decrease toward the surface more continuously than organic matter and at intermediate depths is essentially absent in the presence of high levels of organic matter. These results suggest that organic matter weathering in shales can be treated in terms of the reaction of organic matter with gaseous O_2 and O_2 dissolved in groundwater. Once a weathering profile is developed the inward or downward migrating O_2 reacts first with modem soil organic matter and subsequently with low concentrations of remaining pyrite and ancient organic matter before reaching the "front". Pyrite apparently reacts faster with O_2 than does organic matter (for a given local concentration of oxygen) as evidenced by reduced pyrite concentrations accompanying high organic matter concentrations at the front. Upon further inward migration lower levels of O_2 react with higher concentrations of pyrite and organic matter. These data provide an important basis for the theoretical modeling of organic matter oxidation during weathering.
机译:为了研究沉积有机物的风化及其在调节大气中氧气的作用,对新奥尔巴尼组(上泥盆统,肯塔基州克莱市)黑色页岩钻芯的总碳,有机碳,氮,磷和总氮进行了分析。硫,用于孔隙率,渗透性和比表面积。页岩中有机物和黄铁矿的分布也已经通过电子显微照相和元素映射的方法进行了研究。元素映射表明,页岩有机质主要以0.5至50μm的盘状凝块和不连续的薄片(“纵梁”)存在,而不是以粘土颗粒上的单分子涂层形式存在。氧化风化引起的有机物流失发生在整个反应“前沿”,有机碳含量与有机氮和硫一起向着陆地表面急剧下降,但在相同深度范围内保持相对恒定的有机磷则没有。伴随有机物减少的是孔隙率的增加。这些结果与早期在单个地层上的研究结果相符,该研究还发现,有机物的氧含量在相似的碳氧化锋面附近朝向陆地表面急剧增加。发现在芯和层中的黄铁矿都比有机物更连续地朝向表面减少,并且在中等深度下,在存在高含量有机物的情况下基本上不存在。这些结果表明,可以通过有机物与溶解在地下水中的气态O_2和O_2的反应来处理页岩中的有机物风化。一旦形成了风化特征,向内或向下迁移的O_2首先与现代土壤有机物发生反应,然后在到达“前沿”之前与低浓度的剩余黄铁矿和古老有机物发生反应。黄铁矿与O_2的反应明显快于有机物(对于给定的局部氧浓度),与有机物的反应更快,这可以从前面伴随着高有机物浓度的黄铁矿浓度降低来证明。在进一步向内迁移时,较低水平的O_2与较高浓度的黄铁矿和有机物发生反应。这些数据为风化过程中有机物氧化的理论模型提供了重要依据。

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