M. J. Toplis’s research while affiliated with Research Institute in Astrophysics and Planetology, French National Centre for Scientific Research and other places

Planetary exploration relies considerably on mineral characterization to advance our understanding of the solar system, the planets and their evolution. Thus, we must understand past and present processes that can alter materials exposed on the surface, affecting space mission data. Here, we analyze the first dataset monitoring the evolution of a known mineral target in situ on the Martian surface, brought there as a SuperCam calibration target onboard the Perseverance rover. We used Raman spectroscopy to monitor the crystalline state of a synthetic apatite sample over the first 950 Martian days (sols) of the Mars2020 mission. We note significant variations in the Raman spectra acquired on this target, specifically a decrease in the relative contribution of the Raman signal to the total signal. These observations are consistent with the results of a UV-irradiation test performed in the laboratory under conditions mimicking ambient Martian conditions. We conclude that the observed evolution reflects an alteration of the material, specifically the creation of electronic defects, due to its exposure to the Martian environment and, in particular, UV irradiation. This ongoing process of alteration of the Martian surface needs to be taken into account for mineralogical space mission data analysis.

Séítah is the stratigraphically lowest formation visited by Perseverance in the Jezero crater floor. We present the data obtained by SuperCam: texture by imagery, chemistry by Laser‐Induced Breakdown Spectroscopy, and mineralogy by Supercam Visible and Infrared reflectance and Raman spectroscopy. The Séítah formation consists of igneous, weakly altered rocks dominated by millimeter‐sized grains of olivine with the presence of low‐Ca and high‐Ca pyroxenes, and other primary minerals (e.g., plagioclase, Cr‐Fe‐Ti oxides, phosphates). Along a ∼140 m long section in Séítah, SuperCam analyses showed evidence of geochemical and mineralogical variations, from the contact with the overlying Máaz formation, going deeper in the formation. Bulk rock and olivine Mg#, grain size, olivine content increase gradually further from the contact. Along the section, olivine Mg# is not in equilibrium with the bulk rock Mg#, indicating local olivine accumulation. These observations are consistent with Séítah being the deep ultramafic member of a cumulate series derived from the fractional crystallization and slow cooling of the parent magma at depth. Possible magmatic processes and exhumation mechanisms of Séítah are discussed. Séítah rocks show some affinity with some rocks at Gusev crater, and with some Martian meteorites suggesting that such rocks are not rare on the surface of Mars. Séítah is part of the Nili Fossae regional olivine‐carbonate unit observed from orbit. Future exploration of Perseverance on the rim and outside of the crater will help determine if the observations from the crater floor can be extrapolated to the whole unit or if this unit is composed of distinct sub‐units with various origins.

The petrologic and geochemical diversity of meteorites is a function of the bulk composition of their parent bodies, but also the result of how and when internal differentiation took place. Here we focus on this second aspect considering the two principal parameters involved: size and accretion time of the body. We discuss the interplay of the various time scales related to heating, cooling and drainage of silicate liquids. Based on two phase flow modelling in 1-D spherical geometry, we show that drainage time is proportional to two independent parameters: μm/R2, the ratio of the matrix viscosity to the square of the body radius and μf/a2, the ratio of the liquid viscosity to the square of the matrix grain size. We review the dependence of these properties on temperature, thermal history and degree of melting, demonstrating that they vary by several orders of magnitude during thermal evolution. These variations call into question the results of two phase flow modelling of small body differentiation that assume constant properties. For example, the idea that liquid migration was efficient enough to remove ²⁶Al heat sources from the interior of bodies and dampen their melting (e.g. Moskovitz and Gaidos, 2011; Neumann et al., 2012) relies on percolation rates of silicate liquids overestimated by six to eight orders of magnitude. In bodies accreted during the first few million years of solar-system history, we conclude that drainage cannot prevent the occurrence of a global magma ocean. These conditions seem ideal to explain the generation of the parent-bodies of iron meteorites. A map of the different evolutionary scenarios of small bodies as a function of size and accretion time is proposed.

Ilmenite-, magnetite- and clinopyroxene−melt trace element partition coefficients were investigated experimentally as a function of oxygen fugacity and melt composition in a range of synthetic ferrobasaltic bulk compositions. The experiments were performed at a constant temperature (1080 °C) and pressure (1 atm) over a range of oxygen fugacity (fO2) conditions from ca. 2 log units below to ca. 2 log units above the FMQ buffer. The partitioning behaviour of the divalent cations Zn, Mn, Co and Ni are found to be controlled by the degree of polymerisation of the coexisting melt; the partitioning behaviour of rare earth elements, Y and Sc can be explained well by the lattice strain model and the partitioning of the high-field strength elements Zr, Hf, Ta and Nb is influenced by the TiO2 content of the melt. Vanadium partitioning is strongly influenced by oxygen fugacity and a series of linear regression equations are presented to express the dependence of the mineral−melt partitioning behaviour of the multivalent cation V on oxygen fugacity. Furthermore, calibration of the partitioning of vanadium between magnetite–ilmenite pairs as an oxybarometer is proposed and applied to a ferrobasaltic layered intrusion—the Skaergaard intrusion—to provide an estimate of oxygen fugacity.

The petrologic and geochemical diversity of meteorites is a function of the bulk composition of their parent bodies, but also the result of how and when internal differentiation took place. Here we focus on this second aspect considering the two principal parameters involved: size and accretion time of the body. We discuss the interplay of the various time scales related to heating, cooling and drainage of silicate liquids. Based on two phase flow modelling in 1-D spherical geometry, we show that drainage time is proportional to two independent parameters: $\mu_m/R^2$, the ratio of the matrix viscosity to the square of the body radius and $\mu_f/a^2$, the ratio of the liquid viscosity to the square of the matrix grain size. We review the dependence of these properties on temperature, thermal history and degree of melting, demonstrating that they vary by several orders of magnitude during thermal evolution. These variations call into question the results of two phase flow modelling of small body differentiation that assume constant properties.For example, the idea that liquid migration was efficient enough to remove $^{26}$Al heat sources from the interior of bodies and dampen their melting (e.g. Moskovitz and Gaidos, 2011; Neumann et al., 2012) relies on percolation rates of silicate liquids overestimated by six to eight orders of magnitude. In bodies accreted during the first few million years of solar-system history, we conclude that drainage cannot prevent the occurrence of a global magma ocean. These conditions seem ideal to explain the generation of the parent-bodies of iron meteorites. A map of the different evolutionary scenarios of small bodies as a function of size and accretion time is proposed.