Constraints on the origin of the oxidation state of mantle overlying subduction zones: An example from Simcoe, Washington, USA

Abstract

Type I spinel peridotite xenoliths from Simcoe Volcano, southern Washington (USA), are from lithospheric mantle approximately 65 km inboard from the axis of the subduction-related Cascade Range. Oxygen fugacities calculated from contents of Fe 3+/ΣFe in Simcoe spinels, determined by Mössbauer spectroscopy, are up to 1.4 log units more oxidizing than the FMQ buffer. These are among the most oxidized mantle xenoliths reported, with fugacities substantially higher than those calculated for mantle beneath most of western North America. These results, together with those from amphibole-bearing spinel peridotites from Ichinomegata, Japan ( Wood and Virgo, 1989), provide evidence that the mantle above subduction zones is more oxidized than is oceanic or ancient cratonic mantle. We suggest that oxidation was accomplished by an agent ranging in composition from solute-rich hydrous fluid to water-bearing silicate melt. A qualitative model relating extent of oxidation, duration of the oxidation process, and proportion of the available water (derived from subducting slabs) that oxidizes Fe in subarc mantle peridotite, suggests that such an agent can easily produce the observed extents of oxidation over timescales similar to the typical lifespans of subduction zones. For the Cascade arc with a duration of 50 Ma, the observed oxidation in the Simcoe peridotites can be achieved by reacting about 6–11 % of the available water with the mantle. These results demonstrate that water can make an efficient oxidizing agent, and because of the comparatively low ferric iron contents reported for mantle peridotites from other tectonic settings, oxidation of the mantle by water is mostly restricted to subduction zones where water is recycled from the surface and transferred into the mantle wedge.