An experimental approach to quantify the effect of tetrahedral boron in tourmaline on the boron isotope fractionation between tourmaline and fluid
-
Martin Kutzschbach
, Bernd Wunder
, Robert B. Trumbull , Alexander Rocholl , Anette Meixner and Wilhelm Heinrich
Abstract
This study investigates the effect of tetrahedral B ([4]B) in synthetic tourmaline on the B-isotope fractionation between tourmaline and fluid. This is important for the correct interpretation of B-isotope variations in natural tourmalines containing “excess” B (greater than three atoms per formula unit), which substitutes for Si at tetrahedral sites. Such tourmalines commonly occur in Li, Al-rich pegmatites and have been reported from glaucophane schists that formed at high pressures during subduction.
Tourmaline synthesis experiments were performed in a piston-cylinder apparatus in the system SiO2-Al2O3-B2O3-NaCl-H2O at 4 GPa and 700 °C using different run durations, starting from quartz-γ-Al2O3-H3BO3 solid mixtures and NaCl-solutions. We were able to produce “olenitic” tourmaline with excess B between 1.2 and 2.5 [4]B per formula unit. The B-isotope compositions of the olenitic tourmaline and coexisting fluids were determined by secondary ion mass spectrometry and multi-collector plasma source mass spectrometry to derive isotope fractionation coefficients. The results indicate that for every 10 mol% of total B in tourmaline in tetrahedral coordination, the value of Δ11Btur-fluid is shifted to more negative values by about 1‰ at 700 °C. This is in good agreement with published ab initio calculations and corresponds to an intracrystalline fractionation of B-isotopes between the trigonal B and tetrahedral T sites of tourmaline on the order of 8 ± 5‰, whereby 10B partitions to the T site.
Acknowledgments
F. Couffignal is acknowledged for his support during SIMS analyses. The authors thank U. Dittmann for sample preparation, H.-P. Nabein for help with the XRD analysis and O. Appelt for support during the EMP measurement. DFG founding granted to G. Franz (TU Berlin) and W. Heinrich (GFZ Potsdam) (FR 557/31-1; HE 2015/16-1) is gratefully acknowledged. A. Meixner acknowledges support from the DFG Major Research Instrumentation Program INST 144/308-1. The quality of the manuscript benefitted a lot from the helpful comments of Horst Marschall and Edward Grew.
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Articles in the same Issue
- Special Collection: Rates and Depths of Magma Ascent on Earth
- Multiple-reaction geobarometry for olivine-bearing igneous rocks
- Special Collection: Rates and Depths of Magma Ascent on Earth
- Eruption style and crystal size distributions: Crystallization of groundmass nanolites in the 2011 Shinmoedake eruption
- Special Collection: Nanominerals and Mineral Nanoparticles
- The nanocrystalline structure of basaluminite, an aluminum hydroxide sulfate from acid mine drainage
- Trace element zoning in hornblende: Tracking and modeling the crystallization of a calc-alkaline arc pluton
- Toward the wider application of 29Si NMR spectroscopy to paramagnetic transition metal silicate minerals: Copper(II) silicates
- Extraterrestrial formation of oldhamite and portlandite through thermal metamorphism of calcite in the Sutter’s Mill carbonaceous chondrite
- Age discordance and mineralogy
- Melting relations in the system CaCO3-MgCO3 at 6 GPa
- Electrical conductivity of mudstone (before and after dehydration at high P-T) and a test of high conductivity layers in the crust
- The solubility of CePO4 monazite and YPO4 xenotime in KCl-H2O fluids at 800 °C and 1.0 GPa: Implications for REE transport in high-grade crustal fluids
- Mineralogical, geochemical, and textural indicators of crystal accumulation in the Adamello Batholith (Northern Italy)
- Stability field of the Cl-rich scapolite marialite
- The equation of state of wadsleyite solid solutions: Constraining the effects of anisotropy and crystal chemistry
- An experimental approach to quantify the effect of tetrahedral boron in tourmaline on the boron isotope fractionation between tourmaline and fluid
- A qualitative and quantitative investigation of partitioning and local structure of arsenate in barite lattice during coprecipitation of barium, sulfate, and arsenate
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