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The continental crust is rich in aluminosilicates and formed by the crystallization of arc magmas. However, the magma produced at sub-arc depths is often silica-poor. The chemical evolution of sub-arc magma from silica-poor to aluminosilicate-rich is perplexing. Magnetotelluric (MT) observations in subduction zones and complementary laboratory-based constraints of electrical conductivity (σ) are crucial to understanding this chemical evolution. The σ of a magma is sensitive to pressure (P), temperature (T), and chemistry (X). To date, laboratory-based measurements on the σ of silicate melts have helped to interpret MT observations at P ≤ 2 GPa. Yet, the melting in subduction zones could occur deeper, at P ≤ 6−7 GPa. The σ of melt at such pressures is poorly constrained. To address this, we performed experiments at P ≤ 6 GPa to examine the σ of basaltic to andesitic melts, which are common in subduction zones. We constrained the effects of silica, alumina, alkali, alkaline, and water (H2O) contents on the σ of melt. The activation volume of σ increases with silica contents. Hence, the σ of basaltic melt is overall greater than that of an andesitic counterpart. The σ of basaltic magma is also less sensitive to P than andesitic magma. Water lowers the activation energy and enhances σ for all melt compositions. Our results help constrain how the electrical properties of a magma change with an evolving composition in a subduction zone. 

Abstract Liebermannite (KAlSi₃O₈) is a principal mineral phase expected to be thermodynamically stable in deeply subducted continental and oceanic crusts. The crystal structure of liebermannite exhibits tunnels that are formed between the assemblies of double chains of edge‐sharing (Si, Al) O₆octahedral units, which act as a repository for large incompatible alkali ions. In this study, we investigate the electrical conductivity of liebermannite at 12, 15, and 24 GPa and temperature of 1500 K to track subduction pathways of continental sediments into the Earth's lower mantle. Further, we looked at whether liebermannite could sequester incompatible H₂O at deep mantle conditions. We observe that the superionic conductivity of liebermannite due to the thermally activated hopping of K⁺ions results in high electrical conductivity of more than 1 S/m. Infrared spectral features of hydrous liebermannite indicate the presence of both molecular H₂O and hydroxyl (OH⁻) groups in its crystal structure. The observed high electrical conductivity in the mantle transition zone beneath Northeastern China and the lower mantle beneath the Philippine Sea can be attributed to the subduction pathways of continental sediments deep into the Earth's mantle. While major mineral phases in pyrolitic compositions are almost devoid of H₂O under lower mantle conditions, our study demonstrates that liebermannite could be an important host of H₂O in these conditions. We propose that the relatively high H₂O contents of ocean island basalts derived from deep mantle plumes are primarily related to deeply subducted continental sediments, in which liebermannite is the principal H₂O carrier.