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The relative composition of Earth's core and mantle were set during core formation. By determining how elements partition between metal and silicate at high pressures and temperatures, measurements of the mantle composition and geophysical observations of the core can be used to understand the mechanisms by which Earth formed. Here we present the results of metal‐silicate partitioning experiments for a range of nominally lithophile elements (Al, Ca, K, Mg, O, Si, Th, and U) and S to 85 GPa and up to 5400 K. With our results and a compilation of literature data, we developed a parameterization for partitioning that accounts for compositional dependencies in both the metal and silicate phases. Using this parameterization in a range of planetary growth models, we find that, in general, lithophile element partitioning into the metallic phase is enhanced at high temperatures. The relative abundances of FeO, SiO₂, and MgO in the mantle vary significantly between planetary growth models, and the mantle abundances of these elements can be used to provide important constraints on Earth's accretion. To match Earth's core mass and mantle composition, Earth's building blocks must have been enriched in Fe and depleted in Si compared with CI chondrites. Finally, too little Mg, Si, and O are partitioned into the core for precipitation of oxides to be a major source of energy for the geodynamo. In contrast, several ppb of U can be partitioned into the core at high temperatures, and this energy source must be accounted for in thermal evolution models.

 

Large impact‐melt pockets in shergottites contain both Martian regolith components and sulfide/sulfite bleb clusters that yield high sulfur concentrations locally compared to bulk shergottites. The regolith may be the source of excess sulfur in the shergottite melt pockets. To explore whether shock and release of secondary Fe‐sulfates trapped in host rock voids is a plausible mechanism to generate the shergottite sulfur bleb clusters, we carried out shock recovery experiments on an analog mixture of ferric sulfate and Columbia River basalt at peak pressures of 21 and 31 GPa. The recovered products from the 31 GPa experiment show mixtures of Fe‐sulfide and Fe‐sulfite blebs similar to the sulfur‐rich bleb clusters found in shergottite impact melts. The 21 GPa experiment did not yield such blebs. The collapse of porosity and local high‐strain shear heating in the 31 GPa experiment presumably created high‐temperature hotspots (~2000 °C) sufficient to reduce Fe³⁺to Fe²⁺and to decompose sulfate to sulfite, followed by concomitant reduction to sulfide during pressure release. Our results suggest that similar processes might have transpired during shock production of sulfur‐rich bleb clusters in shergottite impact melts. It is possible that very small CO presence in our experiments could have catalyzed the reduction process. We plan to repeat the experiments without CO.

 

The response of forsterite, Mg₂SiO₄, under dynamic compression is of fundamental importance for understanding its phase transformations and high‐pressure behavior. Here, we have carried out an in situ X‐ray diffraction study of laser‐shocked polycrystalline and single‐crystal forsterite (a‐,b‐, andc‐orientations) from 19 to 122 GPa using the Matter in Extreme Conditions end‐station of the Linac Coherent Light Source. Under laser‐based shock loading, forsterite does not transform to the high‐pressure equilibrium assemblage of MgSiO₃bridgmanite and MgO periclase, as has been suggested previously. Instead, we observe forsterite and forsterite III, a metastable polymorph of Mg₂SiO₄, coexisting in a mixed‐phase region from 33 to 75 GPa for both polycrystalline and single‐crystal samples. Densities inferred from X‐ray diffraction data are consistent with earlier gas‐gun shock data. At higher stress, the response is sample‐dependent. Polycrystalline samples undergo amorphization above 79 GPa. For [010]‐ and [001]‐oriented crystals, a mixture of crystalline and amorphous material is observed to 108 GPa, whereas the [100]‐oriented forsterite adopts an unknown phase at 122 GPa. The first two sharp diffraction peaks of amorphous Mg₂SiO₄show a similar trend with compression as those observed for MgSiO₃in both recent static‐ and laser‐driven shock experiments. Upon release to ambient pressure, all samples retain or revert to forsterite with evidence for amorphous material also present in some cases. This study demonstrates the utility of femtosecond free‐electron laser X‐ray sources for probing the temporal evolution of high‐pressure silicate structures through the nanosecond‐scale events of shock compression and release.

 

Experiments on shock amorphization of plagioclase in Mars-like basalt reconcile the pressure scale for martian meteorites. 

We report the discovery of a dodecagonal quasicrystal Mn 72.3 Si 15.6 Cr 9.7 Al 1.8 Ni 0.6 —composed of a periodic stacking of atomic planes with quasiperiodic translational order and 12-fold symmetry along the two directions perpendicular to the planes—accidentally formed by an electrical discharge event in an eolian dune in the Sand Hills near Hyannis, Nebraska, United States. The quasicrystal, coexisting with a cubic crystalline phase with composition Mn 68.9 Si 19.9 Ni 7.6 Cr 2.2 Al 1.4 , was found in a fulgurite consisting predominantly of fused and melted sand along with traces of melted conductor metal from a nearby downed power line. The fulgurite may have been created by a lightning strike that combined sand with material from downed power line or from electrical discharges from the downed power line alone. Extreme temperatures of at least 1,710 °C were reached, as indicated by the presence of SiO 2 glass in the sample. The dodecagonal quasicrystal is an example of a quasicrystal of any kind formed by electrical discharge, suggesting other places to search for quasicrystals on Earth or in space and for synthesizing them in the laboratory. 

The first test explosion of a nuclear bomb, the Trinity test of 16 July 1945, resulted in the fusion of surrounding sand, the test tower, and copper transmission lines into a glassy material known as “trinitite.” Here, we report the discovery, in a sample of red trinitite, of a hitherto unknown composition of icosahedral quasicrystal, Si₆₁Cu₃₀Ca₇Fe₂. It represents the oldest extant anthropogenic quasicrystal currently known, with the distinctive property that its precise time of creation is indelibly etched in history. Like the naturally formed quasicrystals found in the Khatyrka meteorite and experimental shock syntheses of quasicrystals, the anthropogenic quasicrystals in red trinitite demonstrate that transient extreme pressure–temperature conditions are suitable for the synthesis of quasicrystals and for the discovery of new quasicrystal-forming systems.