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  • 1
    Publication Date: 2021-07-21
    Description: Recent studies have revealed that Earth's deep mantle may have a wider range of oxygen fugacities than previously thought. Such a large heterogeneity might be caused by material subducted into the deep mantle. However, high-pressure phase relations are poorly known in systems including Fe3+ at the top of the lower mantle, where the subducted slab may be stagnant. We therefore conducted high-pressure and high-temperature experiments using a multi-anvil apparatus to study the phase relations in a Fe3+-bearing system at 26 GPa and 1573–2073 K, at conditions prevailing at the top of the lower mantle. At temperatures below 1923 K, MgSiO3-rich bridgmanite, an Fe3+-rich oxide phase, and SiO2 coexist in the recovered sample. Quenched partial melt was observed above 1973 K, which is significantly lower than the solidus temperature of an equivalent Fe3+-free bulk composition. The partial melt obtained from the Fe3+-rich bulk composition has a higher iron content than coexisting bridgmanite, similar to the Fe2+-dominant system. The results suggest that strong mantle oxygen fugacity anomalies might alter the subsolidus and melting phase relations under lower mantle conditions. We conclude that (1) a small amount of melt may be generated from an Al-depleted region of a stagnant slab, such as subducted former banded-iron-formation, and (2) Fe3+ is not transported into the deep part of the lower mantle because of its incompatibility during melting.
    Keywords: 549 ; lower mantle ; redox state ; melting ; bridgmanite ; ferric iron ; stagnant slab
    Language: English
    Type: article
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  • 2
    Publication Date: 2021-07-26
    Description: Ferric iron can be incorporated into the crystal structure of bridgmanite by either oxygen vacancy substitution (MgFeO2.5 component) or charge-coupled substitution (FeFeO3 component) mechanisms. We investigated the concentrations of MgFeO2.5 and FeFeO3 in bridgmanite in the MgO-SiO2-Fe2O3 system at 27 GPa and 1700–2300 K using a multianvil apparatus. The FeFeO3 content increases from 1.6 to 7.6 mol.% and from 5.7 to 17.9 mol.% with and without coexistence of (Mg,Fe)O, respectively, with increasing temperature from 1700 to 2300 K. In contrast, the MgFeO2.5 content does not show clear temperature dependence, that is, ~2–3 and 〈 2 mol.% with and without the coexistence of (Mg,Fe)O, respectively. Therefore, the presence of (Mg,Fe)O enhances the oxygen vacancy substitution for Fe3+ in bridgmanite. It is predicted that Fe3+ is predominantly substituted following the oxygen vacancy mechanism in (Mg,Fe)O-saturated Al-free bridgmanite when Fe3+ is below ~0.025 pfu, whereas the charge-coupled mechanism occurs when Fe3+ 〉 0.025 pfu.
    Keywords: 549 ; bridgmanite ; ferric iron ; oxygen vacancy substitution ; charge-coupled substitution ; lower mantle
    Language: English
    Type: article
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  • 3
    Publication Date: 2021-07-26
    Description: We report the stability and solubility of the FeAlO3 component in bridgmanite based on phase relations in the system MgSiO3-FeAlO3 at 27 GPa and 2000 K using a multi-anvil apparatus combined with in situ synchrotron X-ray diffraction measurements. The results demonstrate that the FeAlO3 component dominates Fe3+ and Al3+ substitution in bridgmanite, although trace amounts of oxygen- and Mg-site vacancy components are also present. Bridgmanite with more than 40 mol% FeAlO3 transforms into the LiNbO3-type phase upon decompression. The FeAlO3 end-member decomposes into corundum and hematite and does not form single-phase bridgmanite. We determined the maximum solubility of the FeAlO3 component in bridgmanite at 27 GPa and 2000 K to be 67 mol%, which is significantly higher than previously reported values (25–36 mol%). We determined the partial molar volume (27.9 mol/cm3) and bulk modulus (197 GPa) of hypothetical FeAlO3 bridgmanite, which are significantly higher and lower than those of AlAlO3 and FeSiO3 bridgmanite, respectively. The non-ideality of MgSiO3-FeAlO3 solid solution (W = 13 kJ/mol, where W is the interaction parameter) is significantly larger than that for MgSiO3-AlAlO3 (5 kJ/mol) and MgSiO3-FeSiO3 (3 kJ/mol) solid solutions. The rapid decrease in abundance of the MgAlO2.5 component in bridgmanite with increasing pressure is enhanced by the presence of the FeAlO3 component. The FeAlO3 content in pyrolite and mid-ocean ridge basalt is far below its solubility limit in bridgmanite and provides new insight into the mineralogy of the lower mantle.
    Keywords: 549 ; bridgmanite ; FeAlO3 solubility ; the LiNbO3-type phase ; non-ideality ; lower mantle
    Language: English
    Type: article
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  • 4
    Publication Date: 2022-01-25
    Description: Molecular hydrogen (H2) released during serpentinization of mantle rocks is one of the main fuels for chemosynthetic life. Processes of H2 production at slow-spreading mid-ocean ridges (MORs) have received much attention in the past. Less well understood is serpentinization at passive continental margins where different rock types are involved (lherzolite instead of harzburgite/dunite at MORs) and the alteration temperatures tend to be lower (〈200°C vs. 〉200°C). To help closing this knowledge gap we investigated drill core samples from the West Iberia margin. Lherzolitic compositions and spinel geochemistry indicate that the exhumed peridotites resemble sub-continental lithospheric mantle. The rocks are strongly serpentinized, mainly consist of serpentine with little magnetite, and are generally brucite-free. Serpentine can be uncommonly Fe- rich, with XMg Mg/(Mg + Fe) 〈 0.8, and shows distinct compositional trends toward a cronstedtite endmember. Bulk rock and silicate fraction Fe(III)/ Fe ratios are 0.6–0.92 and 0.58–0.8, respectively; our data show that 2/3 of the ferric Fe is accounted for by Fe(III)- serpentine. Mass balance and thermodynamic calculations suggest that the sample’s initial serpentinization produced ∼120 to 〉300 mmol H2 per kg rock. The cold, late-stage weathering of the serpentinites at the seafloor caused additional H2 formation. These results suggest that the H2 generation potential evolves during the transition from continental break-up to ultraslow and, eventually, slow MOR spreading. Metamorphic phase assemblages systematically vary between these settings, which has consequences for H2 yields during serpentinization. At magma-poor rifted margins and ultraslow- spreading MORs, serpentine hosts most Fe(III). Hydrogen yields of 120 to 〉300 mmol and 50–150 mmol H2 per kg rock, respectively, may be expected at temperatures of 〈200°C. At slow-spreading MORs, in contrast, serpentinization may produce 200–350 mmol H2, most of which is related to magnetite formation at 〉200°C. Since, in comparison to slow-spreading MORs, geothermal gradients at magma-poor margins and ultraslow-spreading MORs are lower, larger volumes of low-temperature serpentinite should form in these settings. Serpentinization of lherzolitic rocks at magma-poor margins should produce particularly high amounts of H2 under conditions within the habitable zone. Magma-poor margins may hence be more relevant environments for hydrogenotrophic microbial life than previously thought.
    Description: research
    Keywords: serpentinization ; hydrogen generation ; magma-poor rifted margin ; mid-ocean ridges ; ultraslow spreading ; hydrothermal alteration ; chemosynthetic life ; seafloor weathering ; FID-GEO-DE-7
    Language: English
    Type: map
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