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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.
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Insights on the deep carbon cycle from the electrical conductivity of carbon-bearing aqueous fluids
Abstract The dehydration and decarbonation in the subducting slab are intricately related and the knowledge of the physical properties of the resulting C–H–O fluid is crucial to interpret the petrological, geochemical, and geophysical processes associated with subduction zones. In this study, we investigate the C–H–O fluid released during the progressive devolatilization of carbonate-bearing serpentine-polymorph chrysotile, with in situ electrical conductivity measurements at high pressures and temperatures. The C–H–O fluid produced by carbonated chrysotile exhibits high electrical conductivity compared to carbon-free aqueous fluids and can be an excellent indicator of the migration of carbon in subduction zones. The crystallization of diamond and graphite indicates that the oxidized C–H–O fluids are responsible for the recycling of carbon in the wedge mantle. The carbonate and chrysotile bearing assemblages stabilize dolomite during the devolatilization process. This unique dolomite forming mechanism in chrysotile in subduction slabs may facilitate the transport of carbon into the deep mantle.
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- Award ID(s):
- 1753125
- PAR ID:
- 10224271
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Scientific Reports
- Volume:
- 11
- Issue:
- 1
- ISSN:
- 2045-2322
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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