Oxygen isotope fractionation in hematite and magnetite; a theoretical calculation and application to geothermometry of metamorphic iron-formations
Oxygen isotope fractionation in hematite and magnetite; a theoretical calculation and application to geothermometry of metamorphic iron-formations
European Journal of Mineralogy (October 1991) 3 (5): 877-886
- Australasia
- Australia
- Brazil
- chemical fractionation
- chemically precipitated rocks
- Hamersley Range
- hematite
- iron formations
- isotope ratios
- isotopes
- magnetite
- metamorphism
- Minas Gerais Brazil
- O-18/O-16
- oxides
- oxygen
- P-T conditions
- Quadrilatero Ferrifero
- sedimentary rocks
- South America
- stable isotopes
- Western Australia
The application of the modified increment method provides original thermodynamic isotope factors (beta -factors) of O in hematite and magnetite which show that a consistently different isotopic behaviour can be expected for these two minerals. The partition of O isotopes in hematite and magnetite is determined by crystal structure and cation distribution features. Hematite is depleted in (super 18) O relative to magnetite; this matches with observations from the Precambrian iron formation in the Hamersley Range, Australia. Previous experimental calibration of the magnetite- water system by reduction of hematite to magnetite is agreement with the present result for the hematite-water system. This is attributed to the quantitative redox of iron in the experiments that in turn can explain the nearlyidentical isotope composition of O in coexisting hematite and magnetite pairs from the banded iron formation of the Iron Quadrangle, Brazil.