10-100℃海水-玄武岩相互作用模拟:控制参数及其对海洋地壳和海水组成的影响

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS
Simon Prause , Barbara I. Kleine-Marshall , Tobias B. Weisenberger , Andri Stefánsson
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引用次数: 0

摘要

海水-玄武岩相互作用过程中的化学反应和元素动员在调节海水与海洋地壳之间的全球元素通量中起着核心作用。本研究采用动力学反应路径模型研究了10-100℃海水对玄武岩蚀变的影响,评估了反应时间、温度、pH、岩石结晶度和CO₂浓度对地壳老化和冷却过程中蚀变矿物形成和海水成分的影响。早期蚀变包括玄武岩玻璃和原生矿物的溶解,释放出Si、Al、Fe、Ca、Mg、Na和K,随后形成氧化物、氢氧化物、黄铁矿、含铁(III)和含铁(II)的粘土、碳酸盐、celadonite和沸石。当CO₂浓度升高时,例如由于深层岩浆脱气,水的pH值保持在微酸性至环中性值之间。相比之下,在较低的CO₂浓度下,与标准海水相对应,玄武岩溶解过程中H+的消耗增加了pH值,使系统更倾向于还原条件,从而有利于沸石、钙硅酸盐和富镁粘土的形成。反应过程、氧化还原条件、pH和CO 2浓度是蚀变矿物学和海水化学的主要控制因素。玄武岩结晶度主要影响反应速率和时间尺度,而对蚀变的矿物学和化学结果影响较小。温度同样主要影响动力学,但也对海水-玄武岩相互作用期间的K通量有额外的影响,K从低于~ 50°C的海水中去除,但在较高温度下加入海水。该模型预测,在地壳老化和冷却过程中,由于粘土矿物和青瓷石的形成,钾和镁的长期汇将显著增加。钙的表现各不相同,在早期碳酸盐形成的过程中,钙大部分被从海水中去除,但由于玄武岩浸出导致地壳老化,钙的释放量越来越大。这些结果强调了在评估海水-玄武岩相互作用在低温热液蚀变和海底风化中的作用时,需要约束控制海水-玄武岩相互作用的关键参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modeling seawater-basalt interaction at 10–100 °C: Controlling parameters and effects on the composition of the oceanic crust and seawater
Chemical reactions and element mobilization during seawater-basalt interaction play a central role in regulating global element fluxes between seawater and the oceanic crust. This study uses kinetic reaction path modeling to investigate basalt alteration by seawater at 10–100 °C, assessing the influence of reaction time, temperature, pH, rock crystallinity and CO₂ concentration on alteration mineral formation and seawater composition during crustal aging and cooling. Early alteration involves dissolution of basaltic glass and primary minerals, releasing Si, Al, Fe, Ca, Mg, Na and K, followed by the formation of oxides, hydroxides, pyrite, Fe(III)- and Fe(II)-bearing clays, carbonates, celadonite and zeolites. At elevated CO₂ concentrations, for example due to deep magmatic degassing, water pH remains buffered at slightly acidic to circumneutral values. In contrast, at lower CO₂ concentrations, corresponding to standard seawater, H+ consumption during basalt dissolution increases pH and drives the system towards more reducing conditions, thereby favoring the formation of zeolites, Ca-silicates and Mg-rich clays. Reaction progress, redox conditions, pH and CO₂ concentration are the primary controls on alteration mineralogy and seawater chemistry. Basalt crystallinity mainly influenced reaction rates and timescales while having minor effects on the mineralogical and chemical outcome of alteration. Temperature likewise mostly affected kinetics but also had an additional effect on K fluxes during seawater-basalt interaction, with K being removed from seawater below ∼50 °C, but added to seawater at higher temperatures. The model predicts significant long-term sinks of both K and Mg due to the formation of clay minerals and celadonite over the course of crustal aging and cooling. Calcium behaved variably, being mostly removed from seawater by early carbonate formation but becoming increasingly released over the cause of crustal aging due to basalt leaching. These results emphasize the need to constrain key parameters controlling seawater-basalt interaction when evaluating its role in low-temperature hydrothermal alteration and seafloor weathering.
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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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