New Perspectives on Abiotic Organic Synthesis and Processing during Hydrothermal Alteration of the Oceanic Lithosphere

M. Andréani, B. Ménez
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引用次数: 15

Abstract

The main known organic compounds on Earth are biologically derived, whether they are direct products of biological activity or the result of thermal degradation of bio-derived material. While the synthesis of organic compounds from inorganic reactants is a common process in the chemical industry, it remains an unverified component of the deep carbon cycle on Earth and possibly on other planetary bodies. Abiotic organic synthesis is central to life emergence and sustainability, and possibly to “geo-inspired” resources. Intensive efforts are still needed to unravel the possible forms, sources, quantities, and formation mechanisms of abiotic carbon compounds under geologically relevant conditions. An improved knowledge of their processing within the lithosphere is also mandatory to better quantify their impact on biogeochemical cycles and their contribution to C fluxes between Earth’s external and internal envelops. Their presence in fluids and rocks may also affect the kinetics of fluid–silicate reactions and the fates of other elements, particularly the redox-sensitive ones (e.g. transition metals, S). Abiotic organic compounds in the lithosphere can have two main origins: either rising from a deep volcanic source in the mantle or formed in situ in the upper lithosphere during hydrothermal processes from mantellic or seawater inorganic carbon compounds (see Refs. 1 and 2 for reviews). In the present chapter, we focus on lithospheric hydrothermal processes that include late magmatic stages and fluid–rock reactions. In fluids, natural occurrences of recognized abiotic organic volatiles of hydrothermal origin include methane (CH4), short-chain alkanes, and small organic acids. They have mainly been observed in geothermal systems or continental seepages within ophiolites and Precambrian shields and at hydrothermal vents near mid-ocean ridges and subduction forearcs. Hence, they are not necessarily associated with deep active volcanism, and they attest to the contribution of lithospheric hydrothermal processes to abiotic organic synthesis. In most cases, these occurrences of organic volatiles are associated with high concentrations of H2 reached by reduction of water during aqueous alteration of ferrous iron-bearing minerals. The latter are particularly abundant in mantle and olivine-rich lithologies whose alteration process is known as serpentinization.
海洋岩石圈热液蚀变过程中非生物有机合成与加工的新视角
地球上已知的主要有机化合物是生物衍生的,无论它们是生物活性的直接产物还是生物衍生材料热降解的结果。虽然从无机反应物中合成有机化合物是化学工业中一个常见的过程,但它仍然是地球上(可能在其他行星上)深层碳循环的一个未经证实的组成部分。非生物有机合成是生命出现和可持续性的核心,可能也是“地理启发”资源的核心。在地质条件相关的条件下,非生物碳化合物的可能形态、来源、数量和形成机制仍需深入研究。为了更好地量化它们对生物地球化学循环的影响及其对地球内外包膜之间碳通量的贡献,还必须改进对它们在岩石圈内的加工过程的了解。它们在流体和岩石中的存在也可能影响流体-硅酸盐反应的动力学和其他元素的命运,特别是对氧化还原敏感的元素(如过渡金属,S)。岩石圈中的非生物有机化合物可以有两个主要来源:要么来自地幔深处的火山源,要么是在地幔或海水中无机碳化合物的热液过程中在岩石圈上部原位形成的(见参考文献1和2)。在本章中,我们主要讨论岩石圈热液过程,包括岩浆晚期阶段和流体-岩石反应。在流体中,公认的热液来源的非生物有机挥发物包括甲烷(CH4)、短链烷烃和小有机酸。它们主要存在于蛇绿岩和前寒武纪盾内的地热系统或大陆渗漏层以及洋中脊和俯冲前弧附近的热液喷口。因此,它们不一定与深部活火山作用有关,它们证明了岩石圈热液过程对非生物有机合成的贡献。在大多数情况下,这些有机挥发物的出现与含铁铁矿物在水蚀变过程中通过水的还原而达到高浓度的H2有关。后者在地幔和富含橄榄石的岩性中特别丰富,其蚀变过程被称为蛇纹岩化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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