Carbonation and decarbonation reactions: Implications for planetary habitability

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Abstract

The geologic carbon cycle plays a fundamental role in controlling Earth's climate and habitability. For billions of years, stabilizing feedbacks inherent in the cycle have maintained a surface environment that could sustain life. Carbonation/decarbonation reactions are the primary mechanisms for transferring carbon between the solid Earth and the ocean-atmosphere system. These processes can be broadly represented by the reaction: CaSiO3 (wollastonite)+CO2 (gas)CaCO3 (calcite)+SiO2 (quartz). CaSi O3(+ C O2(gas) CaC O3(calcite)+Si O2(quartz). This class of reactions is therefore critical to Earth's past and future habitability. Here, we summarize their significance as part of the Deep Carbon Obsevatory's "Earth in Five Reactions" project. In the forward direction, carbonation reactions like the one above describe silicate weathering and carbonate formation on Earth's surface. Recent work aims to resolve the balance between silicate weathering in terrestrial and marine settings both in the modern Earth system and through Earth's history. Rocks may also undergo carbonation reactions at high temperatures in the ultramafic mantle wedge of a subduction zone or during retrograde regional metamorphism. In the reverse direction, the reaction above represents various prograde metamorphic decarbonation processes that can occur in continental collisions, rift zones, subduction zones, and in aureoles around magmatic systems. We summarize the fluxes and uncertainties of major carbonation/decarbonation reactions and review the key feedback mechanisms that are likely to have stabilized atmospheric CO2 levels. Future work on planetary habitability and Earth's past and future climate will rely on an enhanced understanding of the long-term carbon cycle.

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Stewart, E. M., Ague, J. J., Ferry, J. M., Schiffries, C. M., Tao, R. B., Isson, T. T., & Planavsky, N. J. (2019). Carbonation and decarbonation reactions: Implications for planetary habitability. American Mineralogist, 104(10), 1369–1380. https://doi.org/10.2138/am-2019-6884

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