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David L. Kohlstedt

Researcher at University of Minnesota

Publications -  269
Citations -  22935

David L. Kohlstedt is an academic researcher from University of Minnesota. The author has contributed to research in topics: Creep & Olivine. The author has an hindex of 68, co-authored 262 publications receiving 21370 citations. Previous affiliations of David L. Kohlstedt include Peking University & Cornell University.

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An interconnected network of core-forming melts produced by shear deformation

TL;DR: Experiments are presented which demonstrate that shear deformation to large strains can interconnect a significant fraction of initially isolated pockets of metal and metal sulphide melts in a solid matrix of polycrystalline olivine, indicating that in a dynamic (non-hydrostatic) environment, percolation remains a viable mechanism for the segregation and migration of core-forming melts inA solid silicate mantle.
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Differential stress determined from deformation‐induced microstructures of the Moine Thrust Zone

TL;DR: In this paper, the dislocation structure, recrystallization, and elongation of quartz grains in tectonites from three localities along the Moine thrust fault have been analyzed by transmission electron and optical microscopy.
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The effect of large melt fraction on the deformation behavior of peridotite

TL;DR: In this article, a series of high-temperature, triaxial compressive creep experiments on dry, synthetic peridotites in both the diffusion and dislocation creep regimes were performed.
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Effect of iron content on the creep behavior of olivine: 1. Anhydrous conditions

TL;DR: In this paper, high-temperature, high-pressure triaxial compressive creep experiments were carried out on polycrystalline samples of olivine, (FexMg1−−x)2SiO4, with x≡Fe/(Fe+Mg) = 1.0, 0.75, 0.5, and 0.3.
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Diffusional Creep and Kinetic Demixing in Yttria-Stabilized Zirconia

TL;DR: In this article, the creep behavior of fine-grained yttria-stabilized zirconia with 25 mol% Y2O3 has been characterized as part of an investigation of kinetic demixing in solid-solution oxides which are subjected to a nonhydrostatic state of stress.