Hydrogen isotope ratios in lunar rocks and the delivery of cometary water to the MoonWater plays a critical role in the evolution of planetary bodies 1 , and determination of the amount and sources of lunar water has profound implications for our understanding of the history of the Earth-Moon system. During the Apollo program, the lunar samples were found to be devoid of indigeneous water 2,3 . The severe depletion of lunar volatiles 4 , including water, has long been seen as strong support for the giant-impact origin of the Moon 5 . Recent studies have found water in lunar volcanic glasses 6 and in lunar apatite 7-9 , but the sources of lunar water have not been determined. Here we report ion microprobe measurements of water and hydrogen isotopes in the hydrous mineral apatite, found in crystalline lunar mare basalts and highlands rocks collected during the Apollo missions. We find significant water in apatite from both mare and highlands rocks, indicating a role for water during all phases of the Moon's magmatic history. Variations of hydrogen isotope ratios in apatite suggest the lunar mantle, solar wind protons, and comets as possible sources for water in lunar rocks and imply a significant delivery of cometary water to the Earth-Moon system shortly after the Moon-forming impact.

Oxygen isotopic composition of our solar system is believed to have resulted from mixing of two isotopically distinct nebular reservoirs, 16 O-rich and 17,18 O-rich relative to Earth. The nature and composition of the 17,18 O-rich reservoir are poorly constrained. We report an in situ discovery of a chemically and isotopically unique material distributed ubiquitously in fine-grained matrix of a primitive carbonaceous chondrite Acfer 094. This material formed by oxidation of Fe,Ni-metal and sulfides by water either in the solar nebula or on a planetesimal. Oxygen isotopic composition of this material indicates that the water was highly enriched in 17 O and 18 O (δ 17,18 O SMOW = +180‰ per mil), providing the first evidence for an extremely 17,18 O-rich reservoir in the early solar system.

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Carbonaceous meteorites are thought to be fragments of C-type (carbonaceous) asteroids. Samples of the C-type asteroid (162173) Ryugu were retrieved by the Hayabusa2 spacecraft. We measure the mineralogy, bulk chemical and isotopic compositions of Ryugu samples. They are mainly composed of materials similar to carbonaceous chondrite meteorites, particularly the CI (Ivuna-type) group. The samples consist predominantly of minerals formed in aqueous fluid on a parent planetesimal. The primary minerals were altered by fluids at a temperature of 37 ± 10°C, 5.2 − 0.8 + 0.7 (Stat.) − 2.1 + 1.6 (Syst.) million years after formation of the first solids in the Solar System. After aqueous alteration, the Ryugu samples were likely never heated above ~100°C. The samples have a chemical composition that more closely resembles the Sun’s photosphere than other natural samples do.

The high D/H of the Martian atmosphere (∼5–6 × terrestrial) is considered strong evidence for the loss of Martian water to space. The timing and magnitude of the loss of water from Mars can be constrained by measurements of D/H in Martian meteorites. Previous studies of Martian meteorites have shown a large range in D/H, from terrestrial values to as high as the current Martian atmosphere. Here we show that the ancient (∼4 Ga) Mars meteorite ALH84001 has a D/H 4 × terrestrial and that the young (∼0.17 Ga) Shergotty meteorite has a D/H 5.6 × terrestrial. We also find that the young Los Angeles shergottite has zoning in D/H that can be correlated to igneous growth zoning, strongly suggesting assimilation of D‐enriched water during igneous crystallization near the Martian surface. In contrast to previous studies, we find higher and less variable D/H ratios in these three meteorites. Our results suggest a two‐stage evolution for Martian water—a significant early loss of water to space (prior to 3.9 Ga) followed by only modest loss to space in the last 4 billion years. The current Martian atmospheric D/H has remained essentially unchanged for the last 165 Ma.

Meteorite studies suggest that each solar system object has a unique oxygen isotopic composition. Chondrites, the most primitive of meteorites, have been believed to be derived from asteroids, but oxygen isotopic compositions of asteroids themselves have not been established. We measured, using secondary ion mass spectrometry, oxygen isotopic compositions of rock particles from asteroid 25143 Itokawa returned by the Hayabusa spacecraft. Compositions of the particles are depleted in (16)O relative to terrestrial materials and indicate that Itokawa, an S-type asteroid, is one of the sources of the LL or L group of equilibrated ordinary chondrites. This is a direct oxygen-isotope link between chondrites and their parent asteroid.

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Chondrules and calcium-aluminium-rich inclusions (CAIs) are preserved materials from the early history of the Solar System, where they resulted from thermal processing of pre-existing solids during various flash heating episodes which lasted for several million years. CAIs are believed to have formed about two million years before the chondrules. Here we report the discovery of a chondrule fragment embedded in a CAI. The chondrule's composition is poor in 16O, while the CAI has a 16O-poor melilite (Ca, Mg, Al-Silicate) core surrounded by a 16O-rich igneous mantle. These observations, when combined with the previously reported CAI-bearing chondrules, strongly suggest that the formation of chondrules and CAIs overlapped in time and space, and that there were large fluctuations in the oxygen isotopic compositions in the solar nebula probably synchronizing astrophysical pulses.