Abstract Boron coordination in omphacite and glaucophane was determined by indirect means through the B isotope fractionation among coexisting minerals. Samples from tourmaline-bearing reaction zones in the high-pressure metamorphic mélange on the island of Syros were investigated. These metasomatic zones formed at approximately 0.7 GPa, 415 ±15 °C. Equilibrium B isotope fractionations among paragenetic dravite, phengite, omphacite, and glaucophane were determined by in-situ B isotope analyses using laser-ablation multi-collector ICPMS. The proportions of trigonally and tetrahedrally coordinated B in omphacite and glaucophane were estimated by comparing their boron isotope fractionation relative to dravite (94.6% [3]B and 5.4% [4]B) and phengite (100% [4]B). The B isotope fractionation of omphacite and phengite against dravite are −12.0 ±1.2 ‰ and −13.4 ±2.2 ‰, respectively, where δ11B values of omphacite are 1.9 ±1.6 ‰ higher than in coexisting phengite. No significant isotopic difference was observed between glaucophane and phengite. Consequently, we concluded that in clinopyroxene (omphacite), 88 ±9 % of boron is incorporated in tetrahedral coordination, for example via the B(F,OH)Si-1O-1 substitution, with the remaining 12 ±9 % entering by replacement of SiO4 tetrahedra with BO3 triangles. In contrast, B in glaucophane is exclusively incorporated in the tetrahedrally coordinated sites. The boron coordination in high-pressure minerals that host boron in subducting rocks (clinopyroxene, amphibole, mica) is relevant for modelling B isotope fractionation during slab dehydration in subduction zones.
Read full abstract