Experimental boron isotope fractionation between tourmaline and fluid: confirmation from in situ analyses by secondary ion mass spectrometry and from Rayleigh fractionation modelling

Tourmaline synthesised in an experiment with low boron excess was analysed in situ by secondary ion mass spectrometry. It revealed significant B isotope zonation with ¹¹B/¹⁰B ratios increasing in the growth direction of the crystals. Trend, magnitude and absolute values strongly support results from high-B-excess isotope fractionation experiments. Furthermore, the closed system B-isotopic evolution of the experimental fluid was modelled by Rayleigh fractionation. The model results are in excellent agreement with the measured B-isotope composition of the run-product fluid. Consequently, low-element-excess experiments are proposed as an ideal approach to determine fluid-solid isotope fractionation factors for systems that are characterised by Rayleigh fractionation.