Simon Prause , Barbara I. Kleine-Marshall , Tobias B. Weisenberger , Andri Stefánsson
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引用次数: 0
Abstract
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.
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.