Abstract
Quantitative thermobarometers require selection of a univariant reaction, consideration of dilutions in all phases and application to fully buffered systems. Empirical thermobarometers include AlIV in chlorite, Al in hornblende, Ti in biotite, phengite barometry and various clay and organic transformations. For the most part they were not evaluated with univariant reactions, buffering phases or corrections for solid or fluid solutions and as a result they are not adequately calibrated.
Recently proposed thermometers in the system CaO-ZrO2-TiO2-SiO2 (CazrtiQ) include Ti in zircon, Ti in quartz, Zr in rutile and Zr in sphene. Most of the original calibrations assumed that pressure (P) had no influence on the thermometer despite a significant volume change in buffering reactions. The Zr in sphene was calibrated as a thermobarometer, the P dependence of Ti in zircon and Zr in rutile has now been evaluated and Ti in quartz probably has a P dependence as well. Recent work indicates that zircon thermometer has a −80° to −90°C temperature (T) correction when applied to high level granitic intrusions crystallised at 1–2 kbar and that these are minima in the absence of rutile. Calculations of a(TiO2) from ilmenite-magnetite in the Bishop tuff gives 0.4±0.02, suggesting that granitoids may have a lower a(TiO2) than previously thought, which will shift T back by +30 to +80°C if the zircon can be shown to have equilibrated with the oxides. Combination of thermobarometers in CazrtiQ offers a new set of phase equilibria potentially of wide use in metamorphic and igneous rocks.
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Essene, E.J. (2009). Thermobarometry Gone Astray. In: Gupta, A.K., Dasgupta, S. (eds) Physics and Chemistry of the Earth’s Interior. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-0346-4_6
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