Abstract
Despite the abundance of garnet in deforming regions of the Earth, such as subduction zones, its rheological properties are not well defined by laboratory measurements. Here we report measurements of steady-state plastic properties of pyrope in its stability field (temperature up to 1573 K, pressure up to 6.8 GPa, strain rate ~10-5 s-1) using a Deformation-DIA apparatus (D-DIA) coupled with synchrotron radiation. Synthetic pyrope (Py100) and natural pyrope (Py70Alm16Gr14) are both studied in a dry environment. Transmission electron microscopy (TEM) investigation of the run products indicates that dislocation glide, assisted by climb within grains and dynamic recrystallization for grain-boundary strain accommodation, is the dominant deformation process in pyrope. Both synthetic-and naturalpyropes . stress and strain-rate data, as measured in situ by X-ray diffraction and imaging, are best fitted with the single flow law:

where ε̇ is the strain rate, σ = | σ1-σ3 | is the differential stress, R is the gas constant and T the absolute temperature. Synthetic forsterite and synthetic pyrope were stacked along the uniaxial compression direction in the same cell assembly during deformation to compare their strength at mantle condition. Forsterite is observed to be stronger than pyrope, deforming at a rate about 10% slower than the pyrope at 5.2 GPa and 1573 K. San Carlos olivine and natural pyrope were compared in a similar fashion at 6.8 GPa and 1473 K. In this case, San Carlos olivine deformed 2~3 times faster than natural pyrope. The experimental data suggest that pyrope is stronger (by more than a factor of 4) than the dominant mineral (olivine) in the upper mantle when temperatures exceed 1273 K.
© 2015 by Walter de Gruyter Berlin/Boston
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Articles in the same Issue
- Structural model for the biogenic Mn oxide produced by Pseudomonas putida
- Electron-beam (5–10 keV) damage in triplite-group phosphates: Consequences for electron-microprobe analysis of fluorine
- Vacancy defects in MgO at high pressure
- Plastic flow of pyrope at mantle pressure and temperature
- Parvo-mangano-edenite, parvo-manganotremolite, and the solid solution between Ca and Mn2+ at the M4 site in amphiboles
- Reinvestigation of the MgSiO3 perovskite structure at high pressure
- The mechanism and kinetics of α-NiS oxidation in the temperature range 670–700°C
- Influence of charge location on 29Si NMR chemical shift of 2:1 phyllosilicates
- The size distribution of exsolution lamellae in iron-free clinopyroxene
- The high-pressure phase transformation and breakdown of MgFe2O4
- Elastic behavior, phase transition, and pressure induced structural evolution of analcime
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- Poppiite, the V3+ end-member of the pumpellyite group: Description and crystal structure
- Cation redistribution in the octahedral sheet during diagenesis of illite-smectites from Jurassic and Cambrian oil source rock shales
- A shock-induced polymorph of anatase and rutile from the Chesapeake Bay impact structure, Virginia, U.S.A.
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- Influence of dehydration kinetics on T-O-T bridge breaking in zeolites with framework type STI: The case of stellerite
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