Phase diagrams of hydrous mid-ocean ridge (MOR) basalts to 330 km depth and of hydrous peridotites to 250 km depth are compiled for conditions characteristic for subduction zones. A synthesis of our experimentally determined phase relations of chlorite, lawsonite, epidote-zoisite, amphibole, paragonite, chloritoid, talc, and phengite in basalts and of phase relations from the literature of serpentine, talc, chlorite, amphibole, and phase A in ultramafics permits calculation of H 2 O contents in hydrous phase assemblages that occur in natural compositions. This yields the information necessary to calculate water budgets for descending slabs. Starting from low-grade blueschist conditions (10-20 km depth) with H 2 O contents between 5 and 6 wt% for hydrated oceanic crust, complete dehydration is achieved between 70 and >300 km depth as a function of individual slab geotherms. Hydrous phases which decompose at depth below volcanic arcs are lawsonite, zoisite, chloritoid, and talc (š phengite) in mafic compositions and chlorite and serpentine in peridotite. Approximately 15-35% of the initially subducted H 2 O are released below volcanic arcs. The contribution of amphibole dehydration to the water budget is small (5-20%) and occurs at relatively shallow depth (65-90 km). In any predicted thermal structure, dehydration is a combination of a stepwise and a continuous process through many different reactions which occur simultaneously in the different portions of the descending slab. Such a dehydration characteristic is incompatible with 'single phase dehydration models' which focus fluid flow through a unique major dehydration event in order to explain volcanic fronts. As a consequence of continuously progressing dehydration, water ascending from the slab will be generally available to depth of ca. 150-200 km. The fluid rising from the subducting lithosphere will cause partial melting in the hot portion of the mantle wedge. We propose that the volcanic front simply forms above the mantle wedge isotherm where the extent of melting is sufficient to allow for the mechanical extraction of parental arc magmas. Thermal models show that such an isotherm (ca. 1300ºC) locates below volcanic fronts, slab surface depths below such an isotherm are compatible with the observed depths of the slab surface below volcanic fronts.

Fluids and melts liberated from subducting oceanic crust recycle lithophile elements back into the mantle wedge, facilitate melting and ultimately lead to prolific subduction-zone arc volcanism. The nature and composition of the mobile phases generated in the subducting slab at high pressures have, however, remained largely unknown. Here we report direct LA-ICPMS measurements of the composition of fluids and melts equilibrated with a basaltic eclogite at pressures equivalent to depths in the Earth of 120-180 km and temperatures of 700-1,200 degrees C. The resultant liquid/mineral partition coefficients constrain the recycling rates of key elements. The dichotomy of dehydration versus melting at 120 km depth is expressed through contrasting behaviour of many trace elements (U/Th, Sr, Ba, Be and the light rare-earth elements). At pressures equivalent to 180 km depth, however, a supercritical liquid with melt-like solubilities for the investigated trace elements is observed, even at low temperatures. This mobilizes most of the key trace elements (except the heavy rare-earth elements, Y and Sc) and thus limits fluid-phase transfer of geochemical signatures in subduction zones to pressures less than 6 GPa.

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Very low seismic velocity anomalies in the Earth's mantle may reflect small amounts of melt present in the peridotite matrix, and the onset of melting in the Earth's upper mantle is likely to be triggered by the presence of small amounts of carbonate. Such carbonates stem from subducted oceanic lithosphere in part buried to depths below the 660-kilometre discontinuity and remixed into the mantle. Here we demonstrate that carbonate-induced melting may occur in deeply subducted lithosphere at near-adiabatic temperatures in the Earth's transition zone and lower mantle. We show experimentally that these carbonatite melts are unstable when infiltrating ambient mantle and are reduced to immobile diamond when recycled at depths greater than ∼250 kilometres, where mantle redox conditions are determined by the presence of an (Fe,Ni) metal phase. This 'redox freezing' process leads to diamond-enriched mantle domains in which the Fe(0), resulting from Fe(2+) disproportionation in perovskites and garnet, is consumed but the Fe(3+) preserved. When such carbon-enriched mantle heterogeneities become part of the upwelling mantle, diamond will inevitably react with the Fe(3+) leading to true carbonatite redox melting at ∼660 and ∼250 kilometres depth to form deep-seated melts in the Earth's mantle.