Microstructural Relationship between Olivine and Clinopyroxene in Ultramafic Rocks from the Red Hills Massif, Dun Mountain Ophiolite

Abstract

The microstructural relationship between olivine and clinopyroxene is significant in recovering the mantle evolution under clinopyroxene-saturated melting conditions. This study focuses on olivine/clinopyroxene-related ultramafic rocks (dunite, wehrlite, olivine clinopyroxenite, and clinopyroxenite) in the Ells Stream Complex of the Red Hills Massif. (Olivine) clinopyroxenites have an A/D-type olivine crystallographic preferred orientation (CPO) whereas peridotites have various olivine CPO types. B-type olivine CPO was newly discovered, which may have been generated under hydrous conditions. The discovery of B-type CPO means that all six olivine CPO types could exist in a single research area. Clinopyroxene CPOs also vary and have weaker deformation characteristics (e.g., lower M index and weaker intracrystalline deformation) than olivine; thus, they probably melted and the clinopyroxene-rich ultramafic bands existed as melt veins. Irregular clinopyroxene shapes in the peridotites and incoherent olivine and clinopyroxene CPOs ([100]OL and [001]CPX are not parallel) also indicate a melted state. The dominant orthorhombic and LS-type CPOs in olivine and clinopyroxene imply that simple shear was the main deformation mechanism. Such complicated microstructural characteristics result from the overprinted simple shear under high temperatures (>1000 °C) and hydrous melting environments until the melt-frozen period. This case study is helpful to better understand the olivine and clinopyroxene relationship.