碳循环
碳同位素
化学地层学
碳酸盐
成岩作用
地质学
碳纤维
地球科学
同位素地球化学
沉积岩
海水
稳定同位素比值
碳汇
地球化学
氧同位素比值循环
氧同位素
古生物学
同位素
总有机碳
气候变化
海洋学
环境化学
化学
材料科学
生态学
生态系统
生物
复合数
复合材料
物理
量子力学
有机化学
作者
Anne‐Sofie C. Ahm,Jon M. Husson
标识
DOI:10.1017/9781009028882
摘要
Over million-year timescales, the geologic cycling of carbon controls long-term climate and the oxidation of Earth's surface. Inferences about the carbon cycle can be made from time series of carbon isotopic ratios measured from sedimentary rocks. The foundational assumption for carbon isotope chemostratigraphy is that carbon isotope values reflect dissolved inorganic carbon in a well-mixed ocean in equilibrium with the atmosphere. However, when applied to shallow-water platform environments, where most ancient carbonates preserved in the geological record formed, recent research has documented the importance of considering both local variability in surface water chemistry and diagenesis. These findings demonstrate that carbon isotope chemostratigraphy of platform carbonate rarely represent the average carbonate sink or directly records changes in the composition of global seawater. Understanding what causes local variability in shallow-water settings, and what this variability might reveal about global boundary conditions, are vital questions for the next generation of carbon isotope chemostratigraphers.
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