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Phosphate minerals in ordinary chondrites provide a record of fluids that were present during metamorphic heating of the chondrite parent asteroids. We have carried out a petrographic study of the phosphate minerals, merrillite and apatite, in metamorphosed H group ordinary chondrites of petrologic type 4-6, to understand development of phosphate minerals and associated fluid evolution during metamorphism. In unbrecciated chondrites, apatite is Cl rich and shows textural evolution from fine-grained apatite-merrillite assemblages in type 4 toward larger, uniform grains in type 6. The Cl/F ratio in apatite shows a similar degree of heterogeneity in all petrologic types, and no systematic change in compositions with metamorphic grade, which suggests that compositions in each meteorite are dictated by localized conditions, possibly because of a limited fluid/rock ratio. The development of phosphate minerals in H chondrites is similar to that of L and LL chondrites, despite the fact that feldspar equilibration resulting from albitization is complete in H4 chondrites but not in L4 or LL4 chondrites. This suggests that albitization took place during an earlier period of the metamorphic history than that recorded by preserved apatite compositions, and chemical equilibrium was not achieved throughout the H chondrite parent body or bodies during the late stages of metamorphism. A relict igneous clast in the H5 chondrite, Oro Grande has apatite rims on relict phenocrysts of (possibly) diopside that have equilibrated with the host chondrite. Apatite in the Zag H3-6 regolith breccia records a complex fluid history, which is likely related to the presence of halite in this meteorite. The porous dark H4 matrix of Zag, where halite is observed, has a high apatite/merrillite ratio, and apatite is extremely Cl rich. One light H6 clast contains similarly Cl-rich apatite. In a second light H6 clast, apatite compositions are very heterogeneous and more F-rich. Apatites in both H4 matrix and H6 clasts have very low H2O contents. Heterogeneous apatite compositions in Zag record multiple stages of regolith processing and shock at the surface of the H chondrite parent body, and apatite records either the passage of fluids of variable compositions resulting from different impact-related processes, or the passage of a single fluid whose composition evolved as it interacted with the chondrite regolith. Unraveling the history of apatite can potentially help to interpret the internal structure of chondrite parent bodies, with implications for physical and mechanical properties of chondritic asteroids. The behavior of halogens recorded by apatite is important for understanding the behavior of volatile elements in general: if impact-melt materials close to the surface of a chondritic asteroid are readily degassed, the volatile inventories of terrestrial planets could be considerably more depleted than the CI carbonaceous chondrite abundances that are commonly assumed.

We report the first natural occurrence and single-crystal X-ray diffraction study of the Fe-analog of wadsleyite [a = 5.7485(4), b = 11.5761(9), c = 8.3630(7) Å, V = 556.52(7) Å3; space group Imma], spinelloid-structured Fe2SiO4, a missing phase among the predicted high-pressure polymorphs of ferroan olivine, with the composition (Fe1.102+Mg0.80Cr0.043+Mn0.022+Ca0.02Al0.02Na0.01)# 1S2.01(Si0. 97Al0.03)Σ1.00O4. The new mineral was approved by the International Mineralogical Association (No. 2018-102) and named asimowite in honor of Paul D. Asimow, the Eleanor and John R. McMillan Professor of Geology and Geochemistry at the California Institute of Technology. It was discovered in rare shock-melted silicate droplets embedded in Fe,Ni-metal in both the Suizhou L6 chondrite and the Quebrada Chimborazo (QC) 001 CB3.0 chondrite. Asimowite is rare, but the shock-melted silicate droplets are very frequent in both meteorites, and most of them contain Fe-rich wadsleyite (Fa30-45). Although the existence of such Fe-rich wadsleyite in shock veins may be due to the kinetic reasons, new theoretical and experimental studies of the stability of (Fe,Mg)2SiO4 at high temperature (>1800 K) and pressure are clearly needed. This may also have a significant impact on the temperature and chemical estimates of the mantle's transition zone in Earth.

The short-lived 26Al radionuclide is thought to have been admixed into the initially 26Al-poor protosolar molecular cloud before or contemporaneously with its collapse. Bulk inner Solar System reservoirs record positively correlated variability in mass-independent 54Cr and 26Mg*, the decay product of 26Al. This correlation is interpreted as reflecting progressive thermal processing of infalling 26Al-rich molecular cloud material in the inner Solar System. The thermally unprocessed molecular cloud matter reflecting the nucleosynthetic makeup of the molecular cloud before the last addition of stellar-derived 26Al has not been identified yet but may be preserved in planetesimals that accreted in the outer Solar System. We show that metal-rich carbonaceous chondrites and their components have a unique isotopic signature extending from an inner Solar System composition toward a 26Mg*-depleted and 54Cr-enriched component. This composition is consistent with that expected for thermally unprocessed primordial molecular cloud material before its pollution by stellar-derived 26Al. The 26Mg* and 54Cr compositions of bulk metal-rich chondrites require significant amounts (25–50%) of primordial molecular cloud matter in their precursor material. Given that such high fractions of primordial molecular cloud material are expected to survive only in the outer Solar System, we infer that, similarly to cometary bodies, metal-rich carbonaceous chondrites are samples of planetesimals that accreted beyond the orbits of the gas giants. The lack of evidence for this material in other chondrite groups requires isolation from the outer Solar System, possibly by the opening of disk gaps from the early formation of gas giants.

NASA’S Origins, Spectral Interpretation, Resource Identification and Security-Regolith Explorer (OSIRIS-REx) spacecraft recently arrived at the near-Earth asteroid (101955) Bennu, a primitive body that represents the objects that may have brought prebiotic molecules and volatiles such as water to Earth1. Bennu is a low-albedo B-type asteroid2 that has been linked to organic-rich hydrated carbonaceous chondrites3. Such meteorites are altered by ejection from their parent body and contaminated by atmospheric entry and terrestrial microbes. Therefore, the primary mission objective is to return a sample of Bennu to Earth that is pristine—that is, not affected by these processes4. The OSIRIS-REx spacecraft carries a sophisticated suite of instruments to characterize Bennu’s global properties, support the selection of a sampling site and document that site at a sub-centimetre scale5,6,7,8,9,10,11. Here we consider early OSIRIS-REx observations of Bennu to understand how the asteroid’s properties compare to pre-encounter expectations and to assess the prospects for sample return. The bulk composition of Bennu appears to be hydrated and volatile-rich, as expected. However, in contrast to pre-encounter modelling of Bennu’s thermal inertia12 and radar polarization ratios13—which indicated a generally smooth surface covered by centimetre-scale particles—resolved imaging reveals an unexpected surficial diversity. The albedo, texture, particle size and roughness are beyond the spacecraft design specifications. On the basis of our pre-encounter knowledge, we developed a sampling strategy to target 50-metre-diameter patches of loose regolith with grain sizes smaller than two centimetres4. We observe only a small number of apparently hazard-free regions, of the order of 5 to 20 metres in extent, the sampling of which poses a substantial challenge to mission success.

Metasomatism refers to the process during which a pre-existing rock undergoes compositional and mineralogical transformations associated with chemical reactions triggered by the reaction of fluids which invade the protolith. It changes chemical compositions of minerals, promotes their dissolution and precipitation of new minerals. In this paper, we review metasomatic alteration of type 3 ordinary (H, L, LL) and carbonaceous (CV, CO, CK) chondrites, including ( i ) secondary mineralization, ( ii ) physicochemical conditions, ( iii ) chronology ( 53 Mn- 53 Cr, 26 Al- 26 Mg, 129 I- 129 Xe) of metasomatic alteration, ( iv ) records of metasomatic alteration in H, O, N, C, S, and Cl isotopic systematics, ( v ) effects of metasomatic alteration on O- and Al-Mg-isotope systematics of primary minerals in chondrules and refractory inclusions, and ( vi ) sources of water ices in metasomatically altered CV, CO, and ordinary chondrites, and outline future studies.

The concentration and distribution of water in the Earth has influenced its evolution throughout its history. Even at the trace levels contained in the planet’s deep interior (mantle and core), water affects Earth’s thermal, deformational, melting, electrical and seismic properties, that control differentiation, plate tectonics and volcanism. These in turn influenced the development of Earth’s atmosphere, oceans, and life. In addition to the ubiquitous presence of water in the hydrosphere, most of Earth’s “water” actually occurs as trace amounts of hydrogen incorporated in the rock-forming silicate minerals that constitute the planet’s crust and mantle, and may also be stored in the metallic core. The heterogeneous distribution of water in the Earth is the result of early planetary differentiation into crust, mantle and core, followed by remixing of lithosphere into the mantle after plate-tectonics started. The Earth’s total water content is estimated at 18 − 15 + 81 times the equivalent mass of the oceans (or a concentration of 3900 − 3300 + 32700 ppm weight H 2 O). Uncertainties in this estimate arise primarily from the less-well-known concentrations for the lower mantle and core, since samples for water analyses are only available from the crust, the upper mantle and very rarely from the mantle transition zone (410–670 km depth). For the lower mantle (670–2900 km) and core (2900–4500 km), the estimates rely on laboratory experiments and indirect geophysical techniques (electrical conductivity and seismology). The Earth’s accretion likely started relatively dry because it mainly acquired material from the inner part of the proto-planetary disk, where temperatures were too high for the formation and accretion of water ice. Combined evidence from several radionuclide systems (Pd-Ag, Mn-Cr, Rb-Sr, U-Pb) suggests that water was not incorporated in the Earth in significant quantities until the planet had grown to ∼ 60 – 90 % of its current size, while core formation was still on-going. Dynamic models of planet formation provide additional evidence for water delivery to the Earth during the same period by water-rich planetesimals originating from the asteroid belt and possibly beyond. This early delivered water may have been partly lost during giant impacts, including the Moon forming event: magma oceans can form in their aftermath, degas and be followed by atmospheric loss. More water may have been delivered and/or lost after core formation during late accretion of extraterrestrial material (“late-veneer”). Stable isotopes of hydrogen, carbon, nitrogen and some noble gases in Earth’s materials show similar compositions to those in carbonaceous chondrites, implying a common origin for their water, and only allowing for minor water inputs from comets.

The planetary building blocks that formed in the terrestrial planet region were likely very dry, yet water is comparatively abundant on Earth. Here we review the various mechanisms proposed for the origin of water on the terrestrial planets. Various in-situ mechanisms have been suggested, which allow for the incorporation of water into the local planetesimals in the terrestrial planet region or into the planets themselves from local sources, although all of those mechanisms have difficulties. Comets have also been proposed as a source, although there may be problems fitting isotopic constraints, and the delivery efficiency is very low, such that it may be difficult to deliver even a single Earth ocean of water this way. The most promising route for water delivery is the accretion of material from beyond the snow line, similar to carbonaceous chondrites, that is scattered into the terrestrial planet region as the planets are growing. Two main scenarios are discussed in detail. First is the classical scenario in which the giant planets begin roughly in their final locations and the disk of planetesimals and embryos in the terrestrial planet region extends all the way into the outer asteroid belt region. Second is the Grand Tack scenario, where early inward and outward migration of the giant planets implants material from beyond the snow line into the asteroid belt and terrestrial planet region, where it can be accreted by the growing planets. Sufficient water is delivered to the terrestrial planets in both scenarios. While the Grand Tack scenario provides a better fit to most constraints, namely the small mass of Mars, planets may form too fast in the nominal case discussed here. This discrepancy may be reduced as a wider range of initial conditions is explored. Finally, we discuss several more recent models that may have important implications for water delivery to the terrestrial planets.

Neodynium isotope data reveal that the Earth is enriched in material from red giant stars relative to its presumed meteoritic building blocks, refuting models of a hidden reservoir of 142 Nd-depleted material or a ‘super-chondritic’ Earth. Chondritic meteorites as proxies for Earth's composition Christoph Burkhardt et al . show that, compared to chondritic meteorites, the Earth's precursor bodies were enriched in neodymium produced by the slow neutron capture 's-process' of nucleosynthesis. This s-process excess leads to a higher 142 Nd/ 144 Nd ratio and, after correction for this effect, the 142 Nd/ 144 Nd ratio of chondritic meteorites and the accessible Earth are indistinguishable within five parts per million. The 142 Nd offset between the accessible silicate Earth and chondritic meteorites therefore reflects a higher proportion of s-process neodymium in the Earth, and not early differentiation processes. The authors conclude that there is no need for hidden-reservoir or 'super-chondritic' Earth models, as previously proposed, and that although chondritic meteorites formed at a greater heliocentric distance and contain a different mix of presolar components than the Earth, they nevertheless may be suitable proxies for the Earth's bulk chemical composition. A long-standing paradigm assumes that the chemical and isotopic compositions of many elements in the bulk silicate Earth are the same as in chondrites 1 , 2 , 3 , 4 . However, the accessible Earth has a greater 142 Nd/ 144 Nd ratio than do chondrites. Because 142 Nd is the decay product of the now-extinct 146 Sm (which has a half-life of 103 million years 5 ), this 142 Nd difference seems to require a higher-than-chondritic Sm/Nd ratio for the accessible Earth. This must have been acquired during global silicate differentiation within the first 30 million years of Solar System formation 6 and implies the formation of a complementary 142 Nd-depleted reservoir that either is hidden in the deep Earth 6 , or lost to space by impact erosion 3 , 7 . Whether this complementary reservoir existed, and whether or not it has been lost from Earth, is a matter of debate 3 , 8 , 9 , and has implications for determining the bulk composition of Earth, its heat content and structure, as well as for constraining the modes and timescales of its geodynamical evolution 3 , 7 , 9 , 10 . Here we show that, compared with chondrites, Earth’s precursor bodies were enriched in neodymium that was produced by the slow neutron capture process (s-process) of nucleosynthesis. This s-process excess leads to higher 142 Nd/ 144 Nd ratios; after correction for this effect, the 142 Nd/ 144 Nd ratios of chondrites and the accessible Earth are indistinguishable within five parts per million. The 142 Nd offset between the accessible silicate Earth and chondrites therefore reflects a higher proportion of s-process neodymium in the Earth, and not early differentiation processes. As such, our results obviate the need for hidden-reservoir or super-chondritic Earth models and imply a chondritic Sm/Nd ratio for the bulk Earth. Although chondrites formed at greater heliocentric distances and contain a different mix of presolar components than Earth, they nevertheless are suitable proxies for Earth’s bulk chemical composition.

The Moon was probably formed by a catastrophic collision of the proto-Earth with a planetesimal named Theia. Most numerical models of this collision imply a higher portion of Theia in the Moon than in Earth. Because of the isotope heterogeneity among solar system bodies, the isotopic composition of Earth and the Moon should thus be distinct. So far, however, all attempts to identify the isotopic component of Theia in lunar rocks have failed. Our triple oxygen isotope data reveal a 12 ± 3 parts per million difference in Δ17O between Earth and the Moon, which supports the giant impact hypothesis of Moon formation. We also show that enstatite chondrites and Earth have different Δ17O values, and we speculate on an enstatite chondrite–like composition of Theia. The observed small compositional difference could alternatively be explained by a carbonaceous chondrite–dominated late veneer.