Sound velocity of CaSiO3 perovskite suggests the presence of basaltic crust in the Earth's lower mantle.

Laboratory measurements of sound velocities of high-pressure minerals provide crucial information on the composition and constitution of the deep mantle via comparisons with observed seismic velocities. Calcium silicate (CaSiO3) perovskite (CaPv) is a high-pressure phase that occurs at depths greater than about 560 kilometres in the mantle1 and in the subducting oceanic crust2. However, measurements of the sound velocity of CaPv under the pressure and temperature conditions that are present at such depths have not previously been performed, because this phase is unquenchable (that is, it cannot be physically recovered to room conditions) at atmospheric pressure and adequate samples for such measurements are unavailable. Here we report in situ X-ray diffraction and ultrasonic-interferometry sound-velocity measurements at pressures of up to 23 gigapascals and temperatures of up to 1,700 kelvin (similar to the conditions at the bottom of the mantle transition region) using sintered polycrystalline samples of cubic CaPv converted from bulk glass and a multianvil apparatus. We find that cubic CaPv has a shear modulus of 126 ± 1 gigapascals (uncertainty of one standard deviation), which is about 26 per cent lower than theoretical predictions3,4 (about 171 gigapascals). This value leads to substantially lower sound velocities of basaltic compositions than those predicted for the pressure and temperature conditions at depths between 660 and 770 kilometres. This suggests accumulation of basaltic crust in the uppermost lower mantle, which is consistent with the observation of low-seismic-velocity signatures below 660 kilometres5,6 and the discovery of CaPv in natural diamond of super-deep origin7. These results could contribute to our understanding of the existence and behaviour of subducted crust materials in the deep mantle.

Cubic Fe-bearing majorite synthesized at 18-25 GPa and 1000 °C: implications for element transport, subducted slab rheology and diamond formation.

The chemistry and mineralogy of slabs subducted into lower mantle control slab rheology and impact the deep volatile cycle. It is known that the metamorphism of little-altered oceanic crust results in eclogite rocks with subequal proportions of garnet and clinopyroxene. With increasing pressure, these minerals react to stabilize pyrope-rich tetragonal majoritic garnet. However, some eclogites contain higher proportions of omphacitic clinopyroxene, caused by Na- and Si-rich metasomatism on the ocean floor or during subduction. The mineralogy of such eclogites is expected to evolve differently. Here, we discuss the results of the crystallization products of omphacitic glass at ~ 18 and ~ 25 GPa and 1000 °C to simulate P-T regimes of cold subduction. The full characterization of the recovered samples indicates evidence of crystallization of Na-, Si-rich cubic instead of tetragonal majorite. This cubic majorite can incorporate large amounts of ferric iron, promoting redox reactions with surrounding volatile-bearing fluids and, ultimately, diamond formation. In addition, the occurrence of cubic majorite in the slab would affect the local density, favoring the continued buoyancy of the slab as previously proposed by seismic observations. Attention must be paid to omphacitic inclusions in sublithospheric diamonds as these might have experienced back-transformation from the HP isochemical cubic phase.