Hematite and magnetite precipitates in olivine from the Sulu peridotite: A result of dehydrogenation-oxidation reaction of mantle olivine?
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Shyh-Lung Hwang
,
Hao-Tsu Chu
Abstract
Analytical electron microscopic observations have been carried out on a garnet peridotite from the Maobei area, Sulu ultrahigh-pressure terrane. The results showed that olivine in this garnet peridotite (5.3-6.6 GPa; 853-957 °C), contains precipitates of chromian magnetite and chromian-titanian hematite at dislocations and (001) faults. Specific crystallographic relationships were determined between these precipitates and the olivine host, viz. [101]Mt//[001]Ol, [110]Mt//[01̄1]Ol, and [01̄1]Mt//[011]Ol; and [0001]Hm//[100]Ol and [101̄0]Hm//[001]Ol. These oriented oxides are not associated with silicate/silica phases and therefore cannot be accounted for by the mechanism of olivine oxidation. It is postulated that these magnetite and hematite precipitates most likely have resulted from dehydrogenation-oxidation of nominally anhydrous mantle olivine during rock exhumation. In view of the contrasting diffusion rates of H and Fe in the olivine lattice, it is suggested that the formation process might actually take place in steps. Hydrogen diffusion with concomitant quantitative oxidation of Fe2+ to Fe3+ in olivine occurred early during initial rock exhumation and was followed by slow Fe diffusion forming magnetite/hematite at stacking faults and dislocations within the olivine lattice. Two requirements are essential under such a scenario: an ample amount of H content of the olivine, and an appropriate exhumation rate, probably in the range of 6-11 mm/year, of the host rock. It is also noted that such dehydrogenation-oxidation processes may hamper a correct estimate of the actual P-T conditions and mantle oxidation state based on mineral chemistries present in mantle eclogite/peridotite. The present study demonstrates that oriented mineral inclusions may not necessarily form through exsolution processes sensu stricto, but may form through a series of more complicated reaction mechanisms.
© 2015 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
- Rietveld structure refinement of MgGeO3 post-perovskite phase to 1 Mbar
- High-temperature ammonium white mica from the Betic Cordillera (Spain)
- Synthesis and crystal structure of the feldspathoid CsAlSiO4: An open-framework silicate and potential nuclear waste disposal phase
- The crystal chemistry of Li in gadolinite
- The effect of the hedenbergitic substitution on the compressibility of jadeite
- The structure of monohydrocalcite and the phase composition of the beachrock deposits of Lake Butler and Lake Fellmongery, South Australia
- First-principles calculation of the infrared spectrum of hematite
- In situ observations of muscovite dissolution under alkaline conditions at 25–50 °C by AFM with an air/fluid heater system
- Ramanite-(Cs) and ramanite-(Rb): New cesium and rubidium pentaborate tetrahydrate minerals identified with Raman spectroscopy
- Pressure-temperature studies of talc plus water using X-ray diffraction
- Hematite and magnetite precipitates in olivine from the Sulu peridotite: A result of dehydrogenation-oxidation reaction of mantle olivine?
- Arsenide in a metasomatized peridotite xenolith as a constraint on arsenic behavior in the mantle wedge
- Multiple oxygen sites in synthetic phyllosilicates with expandable layers: 17O solid-state NMR study
- On the existence of a Na-deficient monoclinic trinepheline with composition Na7.85Al7.85Si8.15O32
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- Dense hydrous magnesium silicates, phase D, and superhydrous B: New structural constraints from one- and two-dimensional 29Si and 1H NMR
- Mid-IR bands of synthetic calcic amphiboles of tremolite-pargasite series and of natural calcic amphiboles
- Probing the site occupancies of Co-, Ni-, and Mn-substituted biogenic magnetite using XAS and XMCD
- Origin of titanite in metarodingite from the Zagros Thrust Zone, Iraq
- Experimental calibration of aluminum partitioning between olivine and spinel as a geothermometer
- Single-crystal X-ray diffraction study of CaIrO3
- Orthorhombic polymorph of rengeite from Ohmi region, central Japan
- New insights into the crystal chemistry of epididymite and eudidymite from Malosa, Malawi: A single-crystal neutron diffraction study
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