Magma mixing induced by particle settling.

A time series of experiments at high temperature have been performed to investigate the influence of particle settling on magma mixing. A natural rhyolite glass was held above a natural basalt glass in a platinum crucible. After melting of the glasses at superliquidus temperatures, a platinum sphere was placed on the upper surface of the rhyolitic melt and sank into the experimental column (rhyolitic melt above basaltic melt). Upon falling through the rhyolitic-basaltic melt interface, the Pt sphere entrained a filament of rhyolitic melt in its further fall. The quenched products of the experiments were imaged using X-ray microCT methods. The images of our time series of experiments document the formation of a rhyolite filament as it is entrained into the underlying basalt by the falling platinum sphere. When the Pt particle reached the bottom of the crucible, the entrained rhyolitic filament started to ascend buoyantly up to the initial rhyolitic-basaltic interface. This generated a significant thickness increase of a comingled "melange" layer at the interface due to "liquid rope coiling" and piling up of the filament. As a consequence, the basalt/rhyolite interface was greatly enlarged and diffusive hybridisation greatly accelerated. Further, bubbles, originating at the interface, are observed to have risen into the overlying rhyolite dragging basalt filaments with them. Upon crossing the basalt/rhyolite interface, the bubbles have non-spherical shapes as they adapt to the differing surface tensions of basaltic and rhyolitic melts. Major element profiles, measured across the rhyolite filaments, exhibit asymmetrical shapes from the rhyolite into the basalt. Na and Ti reveal uphill diffusion from the rhyolite towards the interface in the filament cross sections. These results reveal the potential qualitative complexity of the mingling process between rhyolitic and basaltic magmas in the presence of sinking crystals. They imply that crystal-rich magma mingling may be expected to be accelerated with respect to crystal-poor systems. We urge the further fluid dynamic analysis of these phenomena, obtainable for the first time using detailed tomographic imaging.

Concentration variance decay during magma mixing: a volcanic chronometer.

The mixing of magmas is a common phenomenon in explosive eruptions. Concentration variance is a useful metric of this process and its decay (CVD) with time is an inevitable consequence during the progress of magma mixing. In order to calibrate this petrological/volcanological clock we have performed a time-series of high temperature experiments of magma mixing. The results of these experiments demonstrate that compositional variance decays exponentially with time. With this calibration the CVD rate (CVD-R) becomes a new geochronometer for the time lapse from initiation of mixing to eruption. The resultant novel technique is fully independent of the typically unknown advective history of mixing - a notorious uncertainty which plagues the application of many diffusional analyses of magmatic history. Using the calibrated CVD-R technique we have obtained mingling-to-eruption times for three explosive volcanic eruptions from Campi Flegrei (Italy) in the range of tens of minutes. These in turn imply ascent velocities of 5-8 meters per second. We anticipate the routine application of the CVD-R geochronometer to the eruptive products of active volcanoes in future in order to constrain typical "mixing to eruption" time lapses such that monitoring activities can be targeted at relevant timescales and signals during volcanic unrest.