Using Arrested Solid — Solid Multiphase Reactions in Geological Materials to Deduce the Rate of Crustal Uplift
William E. Glassley,Annemarie Meike +1 more
- 13 Mar 2000
- pp 141-154
TL;DR: In this paper, the authors determined the reaction mechanisms responsible for symplectite development, and established the time interval over which these reactions occurred, to constrain the rate of mountain uplift.
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Abstract: The history geological terrains experience can be traced as a series of temperature and pressure changes. Each change drives the system toward a new state of thermodynamic equilibrium. The resultant overprinted rock fabrics, textures and chemical heterogeneities can be difficult to interpret. However, if carefully chosen, features from the scale of kilometers to nanometers can be used to reconstruct the history of mountain systems. Uplift of the Sri Lankan Central Highlands was rapid enough to preserve well-developed symplectite textures, some of which represent arrested solid-state diffusion-controlled reactions of garnet + O2 to form orthopyroxene + plagioclase + magnetite, as the rocks were exhumed from over 30 km in the earth’s crust. Our objective has been to determine the reaction mechanisms responsible for symplectite development, and to establish the time interval over which these reactions occurred, to constrain the rate of mountain uplift. Considering that the most rapid mechanism is solid st te grain-boundary diffusion of oxygen, the reaction time can be constrained by bounding the rate of oxygen supply to the reaction site. The solid state grain boundary diffusion rate of oxygen has been inferred to be ca. 10−14 m2-sec (Farver and Yund, 1991), but is sensitive to inferred grain boundary width. The range of rates thus determined allows the distinction between rapid uplift similar to that of the Himalayan Mountains, and the slow and progressive erosion of a less dramatic terrain. Further constraints on diffusion control and energetic relationships are determined from crystallographic relationships between the reactant and product phases, and submicron scale microstructures.
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References
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TL;DR: In this article, a simplified model for studying grain boundary diffusion of one metal into another was proposed, which has obvious application to the study of heat flow in a poorly conducting solid with a metallic fin.
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The analysis of grain boundary diffusion measurements
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The effect of hydrogen, oxygen, and water fugacity on oxygen diffusion in alkali feldspar
John R. Farver,Richard A. Yund +1 more
TL;DR: Oxygen self-diffusion in adularia and albite single crystals was studied hydrothermally at 650°C from 5 to 1500 MPa confining pressure using a combination of hydrogen/oxygen buffers, a hydrogen ion buffer, and variable mole fractions of water (dilution with CO2) as mentioned in this paper.
103
Grain boundary diffusion of oxygen, potassium and calcium in natural and hot-pressed feldspar aggregates
John R. Farver,Richard A. Yund +1 more
TL;DR: Grain boundary diffusion rates of oxygen, potassium and calcium in fine-grained feldspar aggregates were determined experimentally as mentioned in this paper, and the product of the grain boundary diffusion coefficient (D') and effective boundary width (δ) was calculated using numerical solutions to the appropriate diffusion equation.
91
Volume and grain boundary diffusion of calcium in natural and hot-pressed calcite aggregates
John R. Farver,Richard A. Yund +1 more
TL;DR: In this paper, the authors measured the product of the grain boundary diffusion coefficient (D′) and the effective grain boundary diffusivity width (δ) from 42Ca concentration profiles measured with an ion microprobe and showed that calcium is the slowest volume diffusing species in calcite.
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