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Sulphide oxidation and carbonate dissolution as a source of CO_2 over geological timescales

机译:在地质时间内,硫化物的氧化和碳酸盐的溶解是CO_2的来源

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摘要

The observed stability of Earth's climate over millions of years is thought to depend on the rate of carbon dioxide (CO_2) release from the solid Earth being balanced by the rate of CO_2 consumption by silicate weathering. During the Cenozoic era, spanning approximately the past 66 million years, the concurrent increases in the marine isotopic ratios of strontium, osmium and lithium suggest that extensive uplift of mountain ranges may have stimulated CO_2 consumption by silicate weathering, but reconstructions of sea-floor spreading do not indicate a corresponding increase in CO_2 inputs from volcanic degassing. The resulting imbalance would have depleted the atmosphere of all CO_2 within a few million years. As a result, reconciling Cenozoic isotopic records with the need for mass balance in the long-term carbon cycle has been a major and unresolved challenge in geochemistry and Earth history. Here we show that enhanced sulphide oxidation coupled to carbonate dissolution can provide a transient source of CO_2 to Earth's atmosphere that is relevant over geological timescales. Like drawdown by means of silicate weathering, this source is probably enhanced by tectonic uplift, and so may have contributed to the relative stability of the partial pressure of atmospheric CO_2 during the Cenozoic. A variety of other hypotheses have been put forward to explain the 'Cenozoic isotope-weathering paradox', and the evolution of the carbon cycle probably depended on multiple processes. However, an important role for sulphide oxidation coupled to carbonate dissolution is consistent with records of radiogenic isotopes, atmospheric CO_2 partial pressure and the evolution of the Cenozoic sulphur cycle, and could be accounted for by geologically reasonable changes in the global dioxygen cycle, suggesting that this CO_2 source should be considered a potentially important but as yet generally unrecognized component of the long-term carbon cycle.
机译:据认为,地球气候在数百万年中所观察到的稳定性取决于由固体地球释放的二氧化碳(CO_2)速率与硅酸盐风化引起的CO_2消耗速率之间的平衡。在大约六千六百万年的新生代时期,锶,和锂的海洋同位素比率的同时上升表明,山峰的广泛隆升可能通过硅酸盐风化刺激了CO_2的消耗,但是海底扩散的重建并不表示火山脱气产生的CO_2输入量相应增加。造成的失衡将在几百万年内耗尽所有CO_2的大气。结果,在地球化学和地球历史上,将新生代同位素记录与长期碳循环中质量平衡的需要相协调已成为一项重大且尚未解决的挑战。在这里,我们表明,增强的硫化物氧化作用与碳酸盐的溶解作用相结合,可以为地球大气层提供一个CO_2的瞬时来源,这与地质时间尺度有关。像借助硅酸盐风化作用而产生的沉降一样,该源可能会由于构造隆升而增强,因此可能有助于新生代大气CO_2分压的相对稳定性。提出了多种其他假设来解释“新生代同位素-风化悖论”,并且碳循环的演化可能取决于多个过程。然而,硫化物氧化与碳酸盐溶解耦合的重要作用与放射性同位素记录,大气CO_2分压和新生代硫循环的演化相一致,并且可以通过全球双氧循环的地质合理变化来解释,这表明该CO_2来源应被认为是潜在的重要碳源,但仍是长期碳循环中普遍无法识别的组成部分。

著录项

  • 来源
    《Nature》 |2014年第7492期|346-349|共4页
  • 作者单位

    Department of Earth Sciences, University of Southern California, Los Angeles, California 90089, USA;

    Department of Earth Sciences, University of Southern California, Los Angeles, California 90089, USA;

    MOE Key Laboratory of Surficial Geochemistry, Department of Earth Sciences, Nanjing University, 163 Xianlindadao, Nanjing 210046, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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