The rheology of mafic rocks buried at high to ultra-high-pressure conditions remains enigmatic. Minerals stable at these conditions are mechanically very strong (garnet, omphacite, glaucophane, zoisite, kyanite). Yet, viscous shear zones are commonly reported at depths in fossil collisional and subduction zones. The weakening observed in these shear zones is interpreted as being induced by a transition from grain size insensitive to grain size sensitive creep, in particular with the activation of the dissolution–precipitation creep. However, the exact interplay between deformation, mineral reaction and fluid/mass transfer remains poorly-known.

We have conducted a first series of deformation experiments at eclogite-facies conditions on a 2-phase aggregate representative of mafic rocks. Shear experiments were performed in a new generation of Griggs-type apparatus (Univ. Orléans) at 850°C, and 2.1 GPa with a shear strain rate of 10⁻6 s⁻¹. The starting material consists of mixed powders with < 100 µm sized grains of plagioclase and clinopyroxene from an undeformed sample of the Kågen Gabbro in Northern Norway. Experiments have been conducted with 'as is' (dried at 110°C) starting material and with 0.2% added water.

The mechanical data indicate that the samples are first very strong with a peak differential stress at 1.4 GPa. Then, a significant weakening is observed with a stress decrease by 0.5 GPa. The high-strain sample is characterized by a strain gradient increasing toward the center of the shear zone. Metamorphic reactions occur throughout the sample, but the high-strain areas contain considerably more reaction products than the low-strain areas. The nucleation of new phases leads to a drastic grain size reduction and phase mixing, whose intensities are positively correlated with the strain intensity. The nature, distribution and fabric of the mineral products vary also progressively with the strain intensity.

Our preliminary results indicate that strain at eclogite-facies conditions is preferentially accommodated and localized by dissolution-precipitation processes. Further micro-structural and geochemical analyses are required to quantify the exact interplay between the physical and chemical processes controlling the dissolution-precipitation creep.