Experimental constraints on hydrogen diffusion in garnet

Reynes, Julien; Jollands, Michael; Hermann, Jörg; Ireland, Trevor (2018). Experimental constraints on hydrogen diffusion in garnet. Contributions to mineralogy and petrology, 173(9) Springer-Verlag 10.1007/s00410-018-1492-z

[img] Text
Reynes18.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.

Download (2MB) | Request a copy

The incorporation mechanisms and diffusional loss of hydrogen in garnet have been experimentally investigated. A suite of gem-quality hydrous spessartine- and grossular-rich garnets were analysed by Fourier transform infrared spectroscopy (FTIR) and by ion microprobe (SHRIMP-SI) to determine the calibration coefficients for quantification of FTIR data. The excellent agreement between measured absorption and OH/O indicates that the same molar extinction coefficient can be used for spessartine and grossular. The coefficient of 14400 l mol− 1 cm− 2 proposed by Maldener et al. (Phys Chem Miner 30:337–344, 2003) seems the most appropriate for both minerals. A grossular with 6.4% andradite and 1.6% almandine containing 834 ppm H2O, and an almost pure spessartine with 282 ppm H2O, were selected for diffusion experiments. 1.5-mm cubes of garnets were heated between 12 h and 10 days at 1 atm under various temperature (750–1050 °C) and oxygen fugacity (f O 2 fO2 ) conditions, (ΔQFM + 15.2 to − 3.0). Diffusion profiles were acquired from sections through the cubes using FTIR, with a deconvolution algorithm developed to assess peak-specific behaviour. Different families of peaks have been identified based on their diffusive behaviour, representing hydrogen incorporated in different H-bearing defects. A dominant, fast, strongly f O 2 fO2 -dependent oxidation-related diffusion mechanism is proposed ({M 2+ +H + }+14 O 2 =M 3+ +12 H 2 O) ({M2++H+}+14O2=M3++12H2O) (M=Fe, Mn) with a relatively low activation energy (158 ± 19 kJ mol− 1). This diffusion mechanism is likely restricted by availability of ferrous iron in grossular. At low oxygen fugacity, this diffusion mechanism is shut off and the diffusivity decreased by more than three orders of magnitude. A second, slower hydrogen diffusion mechanism has been observed in minor bands, where charge balance might be maintained by diffusion of cation vacancies, with much higher activation energy (≈ 200–270 kJ mol− 1). Spessartine shows clear differences in peak retentivity suggesting that up to four different H sites might exist. This opens exciting opportunities to use hydrogen diffusion in garnet as speedometer. However, it is essential to constrain the main diffusion mechanisms and the oxygen fugacity in the rocks investigated to obtain timescales for metamorphic or igneous processes.

Item Type:

Journal Article (Original Article)


08 Faculty of Science > Institute of Geological Sciences > Petrology
08 Faculty of Science > Institute of Geological Sciences

UniBE Contributor:

Hermann, Jörg


500 Science > 550 Earth sciences & geology








Jörg Hermann

Date Deposited:

23 Nov 2018 13:53

Last Modified:

25 Nov 2018 02:33

Publisher DOI:






Actions (login required)

Edit item Edit item
Provide Feedback