V51I-02
Compositionally Controlled Volatile Content of Nominally Volatile-Free Minerals in the Continental Upper Mantle of Southern Gondwana (Patagonia & W. Antarctica)

Friday, 18 December 2015: 08:15
308 (Moscone South)
Eve Elizabeth Rooks1, Sally A Gibson1, Philip T Leat2 and Chiara Maria Petrone3, (1)University of Cambridge, Earth Sciences, Cambridge, United Kingdom, (2)NERC British Antarctic Survey, Cambridge, United Kingdom, (3)Natural History Museum, Earth Sciences, London, United Kingdom
Abstract:
H2O and F contents affect many physical and chemical properties of the upper mantle, including melting temperature and viscosity. These elements are hosted by hydrous and F-rich phases, and by modally abundant, nominally-anhydrous/halogen-free mantle minerals, which can potentially accommodate the entire volatile budget of the upper mantle. We present high-precision SIMS analyses of H2O, and F in mantle xenoliths hosted by recently-erupted (5-10 Ka) alkali basalts from south Patagonia (Pali Aike) and older (c. 25 Ma) alkali basalts from localities along the Antarctic Peninsula. Samples are well characterised peridotites and pyroxenites, from a range of depths in the off-craton lithospheric mantle. Minerals are relatively dry: H2O contents of olivine span 0-49 ppm, orthopyroxene 150-235 ppm and clinopyroxene 100-395 ppm, with highest concentrations found in spinel-garnet lherzolites from Pali Aike. These H2O concentrations fall within the global measured range for off-craton mantle minerals. H2O and F are correlated, and the relative compatibility of F in mantle phases is clinopyroxene>orthopyroxene>olivine. However, elevated F concentrations of 100-210 ppm are found in pyroxenites from two Antarctic localities. This elevated F content is not correlated with high H2O, suggesting that these rocks interacted with a F-rich melt. In clinopyroxenes, F concentration is correlated with Ti, and the ratio of M1Ti to M1Al + M1Cr, suggesting a charge balanced substitution.

Consistency between samples (excepting high-F pyroxenites) suggests a constant F-budget, and that concentrations in clinopyroxenes are controlled by mineral chemistry. In orthopyroxene, F correlates with CaO, but no other major or minor elements. Large variability of H2O concentrations within samples is attributed to diffusive loss during ascent. Cl is negligible in all samples, indicating little or no influence of slab fluids from this long-lived subduction zone.