Abstract Pleistocene basalts from Daisen and Mengameyama in the SW Japan volcanic arc of western Honshu are characterized by an abundance of olivine crystals with Fe-rich rims. At Daisen, these have previously been interpreted to have formed from their host melt by equilibrium crystal fractionation and by disequilibrium fractionation during supercooling. Here we use combined electron probe microanalysis, isotopography, transmission electron microscopy and selected area electron diffraction to show that crystal rims are significantly enriched in aluminium (up to c. 1 wt%) and hydrogen (up to c. 10 000 ppm) hosted in oriented low-density amorphous domains. These domains are interpreted to have formed by melting of deuteric and/or post-deuteric metasomatic alteration minerals upon uptake of older olivine crystals into fresh, initially aphyric host melts up to a few hours prior to eruption. It is argued that uptake of variably altered crystals into initially aphyric or sparsely phyric melts may be a common process at subduction zones, and can account for typical disequilibrium textures displayed by arc magmas erupted in SW Japan and elsewhere. Analyses of the altered crystal cargo in arc volcanic rocks therefore provides an important tool for understanding subvolcanic hydrothermal systems and the interaction of ascending melts with such systems. Supplementary material: Olivine mineral chemistry data from two typical Daisen basalts and one typical Mengameyama basalt, and a figure showing the locations of all focussed ion beam (FIB) sections studied here, are available at http://www.geolsoc.org.uk/SUP18760 .

Abstract Minerals of mafic rocks from the SW Japan arc have been studied to deduce P – T –X H2O conditions and their variations in mafic arc magmas. Two-pyroxene thermobarometry of magmas from several volcanoes yields constant temperatures and variable pressures. MELTS fractional crystallization modelling is employed to show that such ‘pseudo-decompression paths’ (PDPs) are artefacts that derive from uptake of pyroxene antecrysts formed at a range of crustal levels by isobaric cooling of previously intruded mafic melts. It is shown that PDPs can be used to constrain oxygen fugacities and initial water contents of the intruded magmas. These constraints, and plagioclase hygrometry, indicate that initial melt H 2 O contents change systematically along the SW Japan arc. Direct determination of hydrogen in olivine by secondary ion mass spectrometry yields consistently low olivine H 2 O contents of 11±4 ppm (1σ), with little, if any, along-arc variations. MELTS modelling indicates that crystallization of calcic plagioclase and olivine dominantly occurs during upper crustal differentiation of mafic melts. The combined data indicate that aphyric melts are released from the mantle wedge, taking up most if not all crystals from previously intruded plutonic rocks during rapid magma ascent to the surface.

Felsic and related veins within mantle-derived peridotite xenoliths from Tallante, Spain, were examined in order to understand the mantle-wedge processes related to the behaviour of Si-rich melt. The thickest part of the vein has a quartz diorite lithology, and is composed mainly of quartz and plagioclase, with pyroxenes, hydrous mineral, apatite, zircon and rutile present as minor phases. The thinner parts are free of quartz and predominantly composed of plagioclase. Orthopyroxene always intervenes between the internal part (plagioclase ± quartz) and host peridotite, indicating that it is a product of interaction between silica-oversaturated melt and olivine. This indicates that a sufficiently high melt/wall rock ratio enabled the melt to retain its silica-oversaturated character. The quartz diorite part has adakite-like geochemical signatures, except for negative Ba, Rb Eu and Sr anomalies, and positive Th and U anomalies. These negative anomalies indicate that fractionation of plagioclase and hydrous minerals was achieved between the upper most mantle and the slab melting zone. The shape of the rare-earth element (REE) pattern of clinopyroxene in quartz diorite is strikingly similar to that of clinopyroxene phenocrysts from Aleutian adakites. However, the former has one order higher REE contents than the latter, except for Eu which shows a prominent negative spike. This feature was caused by the precipitation of large amounts of plagioclase and small amounts of clinopyroxene from a fractionated adakitic melt before and during solidification. This adakitic melt was produced by partial melting of a detached and sinking slab beneath the Betic area in the Tertiary.