新生代
风化作用
碳循环
背景(考古学)
海水
碳纤维
硅酸盐
化学
地球科学
总有机碳
全球变化
海洋化学
环境科学
地质学
环境化学
海平面
海洋学
溶解有机碳
矿物学
生物地球化学循环
碳通量
作者
David G. Evans,Y ROSENTHAL,Jonathan Erez,Hagar Hauzer,Laura J. Cotton,Xiaoli Zhou,Romi Nambiar,P Stassen,Paul N. Pearson,Willem Renema,Pratul Kumar Saraswati,Jonathan A. Todd,C. Sturm,Hagit P. Affek
标识
DOI:10.1073/pnas.2511781122
摘要
A ~fivefold decrease in the atmospheric concentration of CO 2 took place during the Cenozoic. This has often been viewed within the context of silicate weathering changes, although the specific contributions of the potential drivers remain poorly understood. Indeed, it has been alternatively argued that changes in the sea floor spreading rate contributed to the Cenozoic p CO 2 decline, although the magnitude of the decrease means that this is unlikely to account for the entirety of the p CO 2 change. One previously overlooked factor is the concomitant change in the major element composition of seawater, especially the concentration of calcium ([Ca 2+ sw ]), which is typically viewed as responding to processes such as weathering, rather than representing a driver in and of itself. Here, we present the first detailed record of the Cenozoic major ion chemistry of seawater and show that [Ca 2+ sw ] has the potential to control key processes that impact the carbon cycle. Although our record cannot determine whether CO 2 is causally driven by [Ca 2+ sw ], carbon cycle box modeling identifies that this may have been the case. Whether or not [Ca 2+ sw ] indeed directly drove p CO 2 during the Cenozoic principally depends on the strength of the silicate weathering feedback and the magnitude of any possible changes in organic carbon burial, both of which could overwhelm a [Ca 2+ sw ]-driven impact on the carbon cycle. As such, determining the sensitivity of the weathering–climate relationship on million-year timescales is key to resolving whether factors such as seawater major ion composition are important carbon cycle drivers.
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