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The detection of deep reflected S waves on Mars inferred a core size of 1,830 ± 40 km (ref. 1 ), requiring light-element contents that are incompatible with experimental petrological constraints. This estimate assumes a compositionally homogeneous Martian mantle, at odds with recent measurements of anomalously slow propagating P waves diffracted along the core–mantle boundary 2 . An alternative hypothesis is that Mars’s mantle is heterogeneous as a consequence of an early magma ocean that solidified to form a basal layer enriched in iron and heat-producing elements. Such enrichment results in the formation of a molten silicate layer above the core, overlain by a partially molten layer 3 . Here we show that this structure is compatible with all geophysical data, notably (1) deep reflected and diffracted mantle seismic phases, (2) weak shear attenuation at seismic frequency and (3) Mars’s dissipative nature at Phobos tides. The core size in this scenario is 1,650 ± 20 km, implying a density of 6.5 g cm −3 , 5–8% larger than previous seismic estimates, and can be explained by fewer, and less abundant, alloying light elements than previously required, in amounts compatible with experimental and cosmochemical constraints. Finally, the layered mantle structure requires external sources to generate the magnetic signatures recorded in Mars’s crust. We provide observational evidence that suggests the presence of a molten silicate layer above the core of Mars, which is overlain by a partially molten layer, indicating that the core of Mars is smaller than previously thought.

The presence and distribution of preserved organic matter on the surface of Mars can provide key information about the Martian carbon cycle and the potential of the planet to host life throughout its history. Several types of organic molecules have been previously detected in Martian meteorites1 and at Gale crater, Mars. Evaluating the diversity and detectability of organic matter elsewhere on Mars is important for understanding the extent and diversity of Martian surface processes and the potential availability of carbon sources1,5,6. Here we report the detection of Raman and fluorescence spectra consistent with several species of aromatic organic molecules in the Máaz and Séítah formations within the Crater Floor sequences of Jezero crater, Mars. We report specific fluorescence-mineral associations consistent with many classes of organic molecules occurring in different spatial patterns within these compositionally distinct formations, potentially indicating different fates of carbon across environments. Our findings suggest there may be a diversity of aromatic molecules prevalent on the Martian surface, and these materials persist despite exposure to surface conditions. These potential organic molecules are largely found within minerals linked to aqueous processes, indicating that these processes may have had a key role in organic synthesis, transport or preservation.

The mass-independent calcium isotope composition of inner-Solar-System bodies is correlated with their masses and accretion ages, indicating a rapid growth for the precursors of Earth and the Moon during the protoplanetary disk’s lifetime. Like Earth, like moon Variation in the isotopic composition of material within the early inner Solar System is usually thought to reflect spatial heterogeneity in the protoplanetary disk. Martin Schiller and co-authors find that the calcium isotope composition of samples from the parent bodies of ureilite and angrite meteorites, as well as from Vesta, Mars and Earth, are correlated to the masses of their inferred parent asteroids and planets. This provides a proxy for their accretion timescales and implies a rapid 'secular' evolution of the bulk calcium isotope composition of the disk in the rocky-planet-forming region. The authors infer that this secular evolution reflects the introduction of pristine outer-Solar-System material to the thermally processed inner protoplanetary disk associated with the accretion of mass to the proto-Sun. They also conclude that the indistinguishable calcium isotope composition of the Earth and the Moon implies that the Moon-forming impact involved protoplanets that completed their accretion near the end of the disk's lifetime. Nucleosynthetic isotope variability among Solar System objects is often used to probe the genetic relationship between meteorite groups and the rocky planets (Mercury, Venus, Earth and Mars), which, in turn, may provide insights into the building blocks of the Earth–Moon system 1 , 2 , 3 , 4 , 5 . Using this approach, it has been inferred that no primitive meteorite matches the terrestrial composition and the protoplanetary disk material from which Earth and the Moon accreted is therefore largely unconstrained 6 . This conclusion, however, is based on the assumption that the observed nucleosynthetic variability of inner-Solar-System objects predominantly reflects spatial heterogeneity. Here we use the isotopic composition of the refractory element calcium to show that the nucleosynthetic variability in the inner Solar System primarily reflects a rapid change in the mass-independent calcium isotope composition of protoplanetary disk solids associated with early mass accretion to the proto-Sun. We measure the mass-independent 48 Ca/ 44 Ca ratios of samples originating from the parent bodies of ureilite and angrite meteorites, as well as from Vesta, Mars and Earth, and find that they are positively correlated with the masses of their parent asteroids and planets, which are a proxy of their accretion timescales. This correlation implies a secular evolution of the bulk calcium isotope composition of the protoplanetary disk in the terrestrial planet-forming region. Individual chondrules from ordinary chondrites formed within one million years of the collapse of the proto-Sun 7 reveal the full range of inner-Solar-System mass-independent 48 Ca/ 44 Ca ratios, indicating a rapid change in the composition of the material of the protoplanetary disk. We infer that this secular evolution reflects admixing of pristine outer-Solar-System material into the thermally processed inner protoplanetary disk associated with the accretion of mass to the proto-Sun. The identical calcium isotope composition of Earth and the Moon reported here is a prediction of our model if the Moon-forming impact involved protoplanets or precursors that completed their accretion near the end of the protoplanetary disk’s lifetime.

A key stage in planet formation is the evolution of a gaseous and magnetized solar nebula. However, the lifetime of the nebular magnetic field and nebula are poorly constrained. We present paleomagnetic analyses of volcanic angrites demonstrating that they formed in a near-zero magnetic field (<0.6 microtesla) at 4563.5 ± 0.1 million years ago, ~3.8 million years after solar system formation. This indicates that the solar nebula field, and likely the nebular gas, had dispersed by this time. This sets the time scale for formation of the gas giants and planet migration. Furthermore, it supports formation of chondrules after 4563.5 million years ago by non-nebular processes like planetesimal collisions. The 1core dynamo on the angrite parent body did not initiate until about 4 to 11 million years after solar system formation.

The Dawn spacecraft targeted 4 Vesta, believed to be a remnant intact protoplanet from the earliest epoch of solar system formation, based on analyses of howardite-eucrite-diogenite (HED) meteorites that indicate a differentiated parent body. Dawn observations reveal a giant basin at Vesta's south pole, whose excavation was sufficient to produce Vesta-family asteroids (Vestoids) and HED meteorites. The spatially resolved mineralogy of the surface reflects the composition of the HED meteorites, confirming the formation of Vesta's crust by melting of a chondritic parent body. Vesta's mass, volume, and gravitational field are consistent with a core having an average radius of 107 to 113 kilometers, indicating sufficient internal melting to segregate iron. Dawn's results confirm predictions that Vesta differentiated and support its identification as the parent body of the HEDs.

Understanding the nature and origin of the precursor material to terrestrial planets is key to deciphering the mechanisms and timescales of planet formation 1 . Nucleosynthetic variability among rocky Solar System bodies can trace the composition of planetary building blocks 2 – 5 . Here we report the nucleosynthetic composition of silicon (μ 30 Si), the most abundant refractory planet-building element, in primitive and differentiated meteorites to identify terrestrial planet precursors. Inner Solar System differentiated bodies, including Mars, record μ 30 Si deficits of −11.0 ± 3.2 parts per million to −5.8 ± 3.0 parts per million whereas non-carbonaceous and carbonaceous chondrites show μ 30 Si excesses from 7.4 ± 4.3 parts per million to 32.8 ± 2.0 parts per million relative to Earth. This establishes that chondritic bodies are not planetary building blocks. Rather, material akin to early-formed differentiated asteroids must represent a major planetary constituent. The μ 30 Si values of asteroidal bodies correlate with their accretion ages, reflecting progressive admixing of a μ 30 Si-rich outer Solar System material to an initially μ 30 Si-poor inner disk. Mars’ formation before chondrite parent bodies is necessary to avoid incorporation of μ 30 Si-rich material. In contrast, Earth’s μ 30 Si composition necessitates admixing of 26 ± 9 per cent of μ 30 Si-rich outer Solar System material to its precursors. The μ 30 Si compositions of Mars and proto-Earth are consistent with their rapid formation by collisional growth and pebble accretion less than three million years after Solar System formation. Finally, Earth’s nucleosynthetic composition for s -process sensitive (molybdenum and zirconium) and siderophile (nickel) tracers are consistent with pebble accretion when volatility-driven processes during accretion and the Moon-forming impact are carefully evaluated. The nucleosynthetic composition of silicon in meteorites indicates that material akin to early-formed differentiated asteroids must represent a major constituent of terrestrial planets such as Earth and Mars.

The formation and differentiation of planetary bodies are dated using radioactive decay systems, including the short-lived 146Sm-142Nd (T ½ = 103 or 68 Ma) and long-lived 147Sm-143Nd (T ½ = 106 Ga) radiogenic pairs that provide relative and absolute ages, respectively. However, the initial abundance and half-life of the extinct radioactive isotope 146Sm are still debated, weakening the interpretation of 146Sm-142Nd systematics obtained for early planetary processes. Here, we apply the short-lived 26Al-26Mg, 146Sm-142Nd, and long-lived 147Sm-143Sm chronometers to the oldest known andesitic meteorite, Erg Chech 002 (EC 002), to constrain the Solar System initial abundance of 146Sm. The 26Al-26Mg mineral isochron of EC 002 provides a tightly constrained initial δ 26Mg* of −0.009 ± 0.005 ‰ and (26Al/27Al)₀ of (8.89 ± 0.09) × 10−6. This initial abundance of 26Al is the highest measured so far in an achondrite and corresponds to a crystallization age of 1.80 ± 0.01 Myr after Solar System formation. The 146Sm-142Nd mineral isochron returns an initial 146Sm/144Sm ratio of 0.00830 ± 0.00032. By combining the Al-Mg crystallization age and initial 146Sm/144Sm ratio of EC 002 with values for refractory inclusions, achondrites, and lunar samples, the best-fit half-life for 146Sm is 102 ± 9 Ma, corresponding to the physically measured value of 103 ± 5 Myr, rather than the latest and lower revised value of 68 ± 7 Ma. Using a half-life of 103 Ma for 146Sm, the 146Sm/144Sm abundance of EC 002 translates into an initial Solar System 146Sm/144Sm ratio of 0.00840 ± 0.00032, which represents the most reliable and precise estimate to date and makes EC 002 an ideal anchor for the 146Sm-142Nd clock.

Analyses by the CheMin X-ray diffraction instrument on Mars Science Laboratory show that gypsum, bassanite, and anhydrite are common minerals at Gale crater. Warm conditions (∼6 to 30 °C) within CheMin drive gypsum dehydration to bassanite; measured surface temperatures and modeled temperature depth profiles indicate that near-equatorial warm-season surface heating can also cause gypsum dehydration to bassanite. By accounting for instrumental dehydration effects we are able to quantify the in situ abundances of Ca-sulfate phases in sedimentary rocks and in eolian sands at Gale crater. All three Ca-sulfate minerals occur together in some sedimentary rocks and their abundances and associations vary stratigraphically. Several Ca-sulfate diagenetic events are indicated. Salinity-driven anhydrite precipitation at temperatures below ∼50 °C may be supported by co-occurrence of more soluble salts. An alternative pathway to anhydrite via dehydration might be possible, but if so would likely be limited to warmer near-equatorial dark eolian sands that presently contain only anhydrite. The polyphase Ca-sulfate associations at Gale crater reflect limited opportunities for equilibration, and they presage mixed salt associations anticipated in higher strata that are more sulfate-rich and may mark local or global environmental change. Mineral transformations within CheMin also provide a better understanding of changes that might occur in samples returned from Mars.

The formation of a primordial crust is a critical step in the evolution of terrestrial planets but the timing of this process is poorly understood. The mineral zircon is a powerful tool for constraining crust formation because it can be accurately dated with the uranium-to-lead (U–Pb) isotopic decay system and is resistant to subsequent alteration. Moreover, given the high concentration of hafnium in zircon, the lutetium-to-hafnium ( 176 Lu– 176 Hf) isotopic decay system can be used to determine the nature and formation timescale of its source reservoir 1 – 3 . Ancient igneous zircons with crystallization ages of around 4,430 million years (Myr) have been reported in Martian meteorites that are believed to represent regolith breccias from the southern highlands of Mars 4 , 5 . These zircons are present in evolved lithologies interpreted to reflect re-melted primary Martian crust 4 , thereby potentially providing insight into early crustal evolution on Mars. Here, we report concomitant high-precision U–Pb ages and Hf-isotope compositions of ancient zircons from the NWA 7034 Martian regolith breccia. Seven zircons with mostly concordant U–Pb ages define 207 Pb/ 206 Pb dates ranging from 4,476.3 ± 0.9 Myr ago to 4,429.7 ± 1.0 Myr ago, including the oldest directly dated material from Mars. All zircons record unradiogenic initial Hf-isotope compositions inherited from an enriched, andesitic-like crust extracted from a primitive mantle no later than 4,547 Myr ago. Thus, a primordial crust existed on Mars by this time and survived for around 100 Myr before it was reworked, possibly by impacts 4 , 5 , to produce magmas from which the zircons crystallized. Given that formation of a stable primordial crust is the end product of planetary differentiation, our data require that the accretion, core formation and magma ocean crystallization on Mars were completed less than 20 Myr after the formation of the Solar System. These timescales support models that suggest extremely rapid magma ocean crystallization leading to a gravitationally unstable stratified mantle, which subsequently overturns, resulting in decompression melting of rising cumulates and production of a primordial basaltic to andesitic crust 6 , 7 . Isotopic compositions of ancient zircons from the NWA 7034 Martian meteorite suggest that Mars must have formed its primordial crust extremely swiftly, less than 20 million years after the formation of the Solar System.