Abstract
The Ti content of biotite can serve as a geothermometer for graphitic, peraluminous metapelites that contain ilmenite or rutile and have equilibrated at roughly 4-6 kbar. The relationship between Ti- coutent, temperature, and Mg/(Mg + Fe) value was calibrated empirically using an extensive natural biotite data set (529 samples) from western Maine and south-central Massachusetts in combination with the petrogenetic grid of Spear et al. (1999). The calculated Ti-saturation surface is curved such that for a given Mg/(Mg + Fe) value, Ti concentration increases as a function of temperature in a nonlinear' fashion, and for a given temperature Ti concentrations decrease with an increase in Mg/(Mg + Fe). The fit to the Ti-saturation surface can be reformulated as the geothermometric expression: T = {[In(Ti) - a - c(XMg)3]/b}0.333, in which T is temperature in degrees Celsius, Ti is the number of atoms per formula unit (apfu) normalized on the basis of 22 O atoms, XMg is Mg/(Mg + Fe), a = -2.3594, b = 4.6482 x 1O-9 and c = -1.7283. The calibration range for this expression is XMg = 0.275-1.000, Ti = 0.04-0.60 apfu, and T = 480-800 0C. Precision of the Ti-in-biotite geothermometer is estimated to be ±24 0C at the lower temperature range and improves to ±12 °C at higher temperatures. Application of the Ti-in-biotite geothermometer to ilmenite- or rutile-bearing, graphitic, peraluminous metapelites equilibrated at 3-6 kbar is generally consistent with independent temperature determinations, but with some deviations that represent local reequilibration. Consequently, the Ti systematics in biotite can also serve as the basis of a very sensitive indicator of chemical equilibrium, or lack thereof. Application of the geothermometer to metapelites not containing the requisite mineral assemblages can lead to minor-to-significant errors in estimated temperatures.
Biotite Ti-substitution mechanisms are controlled by several factors. Based on the biotite calibration data set, magnesian biotites (XMg> 0.65) incorporate Ti in accordance with the exchange vector TiAl2R-1Si-2, where R is the sum of the divalent cations Mg + Fe + Mn. This substitution mechanism is primarily a response to misfit of the octahedral and tetrahedral layers in magnesian biotites. Intermediate biotites (XMg <0.65), particularly at higher temperatures, exhibit enhanced Ti concentrations, most consistent with the Ti-deprotonation TiO2R-1(OH)-2, exchange vector. Dominance of Ti-deprotonation substitution is largely a function of reduction of H2O activity at higher metamorphic grades. Supplementary biotite data from metaluminous amphibolites and mafic granulites, metamorphosed isothermally with variable H2O activities, reveal that Iow-Al biotite incorporates significantly higher concentrations of Ti relative to peraluminous biotite as a result of a combination of the exchange vectors Ti02R-1(0H)-2 and RSiAl-2, substituting in roughly an 8:1 ratio.
© 2015 by Walter de Gruyter Berlin/Boston
Articles in the same Issue
- Comparative planetary mineralogy: Valence state partitioning of Cr, Fe, Ti, and V among crystallographic sites in olivine, pyroxene, and spinel from planetary basalts
- The origin of orthopyroxene/biotite + plagioclase coronas from the Bolangir anorthosite complex (India), and implications for reconstructing P-T paths
- Dellaventuraite, NaNa2(MgMn23+Ti4+Li)Si8O22O2, a new anhydrous amphibole from the Kajlidongri Manganese Mine, Jhabua District, Madhya Pradesh, India
- Successive zoning of Al and H in hydrothermal vein quartz
- The Ti-saturation surface for low-to-medium pressure metapelitic biotites: Implications for geothermometry and Ti-substitution mechanisms
- Thermochemistry of hydrotalcite-like phases in the MgO-Al2O3-CO2-H2O system: A determination of enthalpy, entropy, and free energy
- Igneous thermometers and barometers based on plagioclase + liquid equilibria: Tests of some existing models and new calibrations
- Thermodynamic properties of the Tschermak solid solution in Fe-chlorite: Application to natural examples and possible role of oxidation
- Experimental data on the Tschermak substitution in Fe-chlorite
- Nanometer-sized, divalent-Mn, hydrous silicate domains in geothermal brine precipitates
- Geometric crystal chemical models for structural analysis of micas and their stacking polytypes
- Fundamental difference between synthetic powder and natural or synthetic single-crystal 1M micas: Geometric homo-octahedral vs. geometric meso-octahedral sheets
- The crystal structures of synthetic Fe2(SO4)3(H2O)5 and the type specimen of lausenite
- Experimental study of plagioclase rim growth around anorthite seed crystals in rhyodacitic melt
- Luminescence study of defects in synthetic as-grown and HPHT diamonds compared to natural diamonds
- Molar absorptivities of OH and H2O in rhyolitic glass at room temperature and at 400600 °C
- Ordering and elasticity associated with low-temperature phase transitions in lawsonite
- Formation of metastable cubic-perovskite in high-pressure phase transformation of Ca(Mg, Fe, Al)Si2O6
- Oxygen isotope heterogeneities and diffusion profile in composite metamorphic-magmatic garnets from the Pyrenees
- Unmixed spinel in chromitite from the Iwanai-dake peridotite complex, Hokkaido, Japan: A reaction between peridotite and highly oxidized magma in the mantle wedge
- Mn-bearing “oxy-rossmanite” with tetrahedrally coordinated Al and B from Austria: Structure, chemistry, and infrared and optical spectroscopic study
- Geochemical applications of the simple salt approximation to the lattice energies of complex materials
- Letter: A method for controlling alkali-metal oxide activities in one-atmosphere experiments and its application to measuring the relative activity coeficients of NaO0.5 in silicate melts
- Letter: Very low solubility of rutile in H2O at high pressure and temperature, and its implications for Ti mobility in subduction zones
- Letter: Microscopic strain in synthetic pyrope-grossular solid solutions determined by synchrotron X-ray powder diffraction at 5 K: The relationship to enthalpy of mixing behavior
- Letter: Ferrous hydroxy carbonate is a stable transformation product of biogenic magnetite
Articles in the same Issue
- Comparative planetary mineralogy: Valence state partitioning of Cr, Fe, Ti, and V among crystallographic sites in olivine, pyroxene, and spinel from planetary basalts
- The origin of orthopyroxene/biotite + plagioclase coronas from the Bolangir anorthosite complex (India), and implications for reconstructing P-T paths
- Dellaventuraite, NaNa2(MgMn23+Ti4+Li)Si8O22O2, a new anhydrous amphibole from the Kajlidongri Manganese Mine, Jhabua District, Madhya Pradesh, India
- Successive zoning of Al and H in hydrothermal vein quartz
- The Ti-saturation surface for low-to-medium pressure metapelitic biotites: Implications for geothermometry and Ti-substitution mechanisms
- Thermochemistry of hydrotalcite-like phases in the MgO-Al2O3-CO2-H2O system: A determination of enthalpy, entropy, and free energy
- Igneous thermometers and barometers based on plagioclase + liquid equilibria: Tests of some existing models and new calibrations
- Thermodynamic properties of the Tschermak solid solution in Fe-chlorite: Application to natural examples and possible role of oxidation
- Experimental data on the Tschermak substitution in Fe-chlorite
- Nanometer-sized, divalent-Mn, hydrous silicate domains in geothermal brine precipitates
- Geometric crystal chemical models for structural analysis of micas and their stacking polytypes
- Fundamental difference between synthetic powder and natural or synthetic single-crystal 1M micas: Geometric homo-octahedral vs. geometric meso-octahedral sheets
- The crystal structures of synthetic Fe2(SO4)3(H2O)5 and the type specimen of lausenite
- Experimental study of plagioclase rim growth around anorthite seed crystals in rhyodacitic melt
- Luminescence study of defects in synthetic as-grown and HPHT diamonds compared to natural diamonds
- Molar absorptivities of OH and H2O in rhyolitic glass at room temperature and at 400600 °C
- Ordering and elasticity associated with low-temperature phase transitions in lawsonite
- Formation of metastable cubic-perovskite in high-pressure phase transformation of Ca(Mg, Fe, Al)Si2O6
- Oxygen isotope heterogeneities and diffusion profile in composite metamorphic-magmatic garnets from the Pyrenees
- Unmixed spinel in chromitite from the Iwanai-dake peridotite complex, Hokkaido, Japan: A reaction between peridotite and highly oxidized magma in the mantle wedge
- Mn-bearing “oxy-rossmanite” with tetrahedrally coordinated Al and B from Austria: Structure, chemistry, and infrared and optical spectroscopic study
- Geochemical applications of the simple salt approximation to the lattice energies of complex materials
- Letter: A method for controlling alkali-metal oxide activities in one-atmosphere experiments and its application to measuring the relative activity coeficients of NaO0.5 in silicate melts
- Letter: Very low solubility of rutile in H2O at high pressure and temperature, and its implications for Ti mobility in subduction zones
- Letter: Microscopic strain in synthetic pyrope-grossular solid solutions determined by synchrotron X-ray powder diffraction at 5 K: The relationship to enthalpy of mixing behavior
- Letter: Ferrous hydroxy carbonate is a stable transformation product of biogenic magnetite