The iodine-plutonium-xenon age of the Moon-Earth system revisited

From iodine-plutonium-xenon isotope systematics, we re-evaluate time constraints on the early evolution of the Earth-atmosphere system and, by inference, on the Moon-forming event. Two extinct radioactivites (129I, T1/2 = 15.6 Ma, and 244Pu, T1/2 = 80 Ma) have produced radiogenic 129Xe and fissiogenic 131-136Xe, respectively, within the Earth, which related isotope fingerprints are seen in the compositions of mantle and atmospheric Xe. Recent studies of Archean rocks suggest that xenon atoms have been lost from the Earth's atmosphere and isotopically fractionated during long periods of geological time, until at least the end of the Archean eon. Here we build a model that takes into account these results. Correction for Xe loss permits to compute new closure ages for the Earth's atmosphere that are in agreement with those computed for mantle Xe. The minimum Xe formation interval for the Earth- atmosphere is 40 (-10+20) Ma after start of solar system formation, which may also date the Moon-forming impact.Comment: 27 pages, 3 figures, 2 table

Perspectives on atmospheric evolution from noble gas and nitrogen isotopes on Earth, Mars & Venus

The composition of an atmosphere has integrated the geological history of the entire planetary body. However, the long-term evolutions of the atmospheres of the terrestrial planets are not well documented. For Earth, there were until recently only few direct records of atmosphere's composition in the distant past, and insights came mainly from geochemical or physical proxies and/or from atmospheric models pushed back in time. Here we review innovative approaches on new terrestrial samples that led to the determination of the elemental and isotopic compositions of key geochemical tracers, namely noble gases and nitrogen. Such approaches allowed one to investigate the atmosphere's evolution through geological period of time, and to set stringent constraints on the past atmospheric pressure and on the salinity of the Archean oceans. For Mars, we review the current state of knowledge obtained from analyses of Martian meteorites, and from the direct measurements of the composition of the present-day atmosphere by rovers and spacecrafts. Based on these measurements, we explore divergent models of the Martian and Terrestrial atmospheric evolutions. For Venus, only little is known, evidencing the critical need for dedicated missions

Origin and significance of cosmogenic signatures in vesicles of lunar basalt 15016

Lunar basalt 15016 (~3.3 Ga) is among the most vesicular (50% by volume) basalts recovered by the Apollo missions. We investigated the possible occurrence of indigenous lunar nitrogen and noble gases trapped in vesicles within basalt 15016, by crushing several cm‐sized chips. Matrix/mineral gases were also extracted from crush residues by fusion with a CO_2 laser. No magmatic/primordial component could be identified; all isotope compositions, including those of vesicles, pointed to a cosmogenic origin. We found that vesicles contained ~0.2%, ~0.02%, ~0.002%, and ~0.02% of the total amount of cosmogenic ^(21)Ne, ^(38)Ar, ^(83)Kr, and ^(126)Xe, respectively, produced over the basalt's 300 Myr of exposure. Diffusion/recoil of cosmogenic isotopes from the basaltic matrix/minerals to intergrain joints and vesicles is discussed. The enhanced proportion of cosmogenic Xe isotopes relative to Kr detected in vesicles could be the result of kinetic fractionation, through which preferential retention of Xe isotopes over Kr within vesicles might have occurred during diffusion from the vesicle volume to the outer space through microleaks. This study suggests that cosmogenic loss, known to be significant for ^3He and ^(21)Ne, and to a lesser extent for ^(36)Ar (Signer et al. 1977), also occurs to a negligible extent for the heaviest noble gases Kr and Xe

Salinity of the Archaean oceans from analysis of fluid inclusions in quartz

Fluids trapped in inclusions in well-characterized Archaean hydrothermal quartz crystals were analyzed by the extended argon–argon method, which permits the simultaneous measurement of chlorine and potassium concentrations. Argon and nitrogen isotopic compositions of the trapped fluids were also determined by static mass spectrometry. Fluids were extracted by stepwise crushing of quartz samples from North Pole (NW Australia) and Barberton (South Africa) 3.5–3.0-Ga-old greenstone belts. The data indicate that fluids are a mixture of a low salinity end-member, regarded as the Archaean oceanic water, and several hydrothermal end-members rich in Cl, K, N, and radiogenic parentless ^(40)Ar. The low Cl–K end-member suggests that the salinity of the Archaean oceans was comparable to the modern one, and that the potassium content of the Archaean oceans was lower than at present by about 40%. A constant salinity of the oceans through time has important implications for the stabilization of the continental crust and for the habitability of the ancient Earth

The origin and degassing history of the Earth's atmosphere revealed by Archean xenon

Xenon (Xe) is an exceptional tracer for investigating the origin and fate of volatile elements on Earth. The initial isotopic composition of atmospheric Xe remains unknown, as do the mechanisms involved in its depletion and isotopic fractionation compared with other reservoirs in the solar system. Here we present high precision analyses of noble gases trapped in fluid inclusions of Archean quartz (Barberton, South Africa) that reveal the isotopic composition of the paleo-atmosphere at ≈3.3 Ga. The Archean atmospheric Xe is mass-dependently fractionated by 12.9±2.4 ‰ u^(−1) (± 2σ, s.d.) relative to the modern atmosphere. The lower than today ^(129)Xe excess requires a degassing rate of radiogenic Xe from the mantle higher than at present. The primordial Xe component delivered to the Earth's atmosphere is distinct from Solar or Chondritic Xe but similar to a theoretical component called U-Xe. Comets may have brought this component to the Earth's atmosphere during the last stages of terrestrial accretion

Stepwise heating of lunar anorthosites 60025, 60215, 65315 possibly reveals an indigenous noble gas component on the Moon

Despite extensive effort during the last four decades, no clear signature of a lunar indigenous noble gas component has been found. In order to further investigate the possible occurrence of indigenous volatiles in the Moon, we have re-analyzed the noble gas and nitrogen isotopic compositions in three anorthosite samples. Lunar anorthosites 60025, 60215 and 65315 have the lowest exposure duration (∼2 Ma) among Apollo samples and consequently contain only limited cosmogenic (e.g. ^(124,126)Xe) and solar wind (SW) noble gases. Furthermore, anorthosites have negligible contributions of fissiogenic Xe isotopes because of their very low Pu and U contents. As observed in previous studies (Lightner and Marti, 1974; Leich and Niemeyer, 1975), lunar anorthosite Xe presents an isotopic composition very close to that of terrestrial atmospheric Xe, previously attributed to “anomalous adsorption” of terrestrial Xe after sample return. The presumed atmospheric Xe contamination can only be removed by heating the samples at medium to high temperatures under vacuum, and is therefore different from common adsorption. To test this hypothesis, we monitored the adsorption of Xe onto lunar anorthositic powder using infrared reflectance spectroscopy. A clear shift in the anorthosite IR absorbance peaks is detected when comparing the IR absorbance spectra of the lunar anorthositic powder before and after exposure to a neutral Xe-rich atmosphere. This observation accounts for the chemical bonding (chemisorption) of Xe onto anorthosite, which is stronger than the common physical bonding (physisorption) and could account for the anomalous adsorption of Xe onto lunar samples. Our high precision Xe isotope analyses show slight mass fractionation patterns across ^(128–136)Xe isotopes with systematic deficits in the heavy Xe isotopes (mostly ^(136)Xe and marginally ^(134)Xe) that have not previously been observed. This composition could be the result of mixing between an irreversibly adsorbed terrestrial contaminant that is mostly released at high temperature and an additional signature. Solar Wind (SW) Xe contents, estimated from SW-Ne and SW-Ar concentrations and SW-Ne/Ar/Xe elemental ratios, do not support SW as the additional contribution. Using a χ^2 test, the latter is best accounted for by cometary Xe as measured in the coma of Comet 67P/Churyumov-Gerasimenko (Marty et al., 2017) or by the primordial U-Xe composition inferred to be the precursor of atmospheric Xe (Pepin, 1994; Avice et al., 2017). It could have been contributed to the lunar budget by volatile-rich bodies that participated to the building of the terrestrial atmosphere inventory (Marty et al., 2017)

Origin and significance of cosmogenic signatures in vesicles of lunar basalt 15016

Lunar basalt 15016 (~3.3 Ga) is among the most vesicular (50% by volume) basalts recovered by the Apollo missions. We investigated the possible occurrence of indigenous lunar nitrogen and noble gases trapped in vesicles within basalt 15016, by crushing several cm‐sized chips. Matrix/mineral gases were also extracted from crush residues by fusion with a CO_2 laser. No magmatic/primordial component could be identified; all isotope compositions, including those of vesicles, pointed to a cosmogenic origin. We found that vesicles contained ~0.2%, ~0.02%, ~0.002%, and ~0.02% of the total amount of cosmogenic ^(21)Ne, ^(38)Ar, ^(83)Kr, and ^(126)Xe, respectively, produced over the basalt's 300 Myr of exposure. Diffusion/recoil of cosmogenic isotopes from the basaltic matrix/minerals to intergrain joints and vesicles is discussed. The enhanced proportion of cosmogenic Xe isotopes relative to Kr detected in vesicles could be the result of kinetic fractionation, through which preferential retention of Xe isotopes over Kr within vesicles might have occurred during diffusion from the vesicle volume to the outer space through microleaks. This study suggests that cosmogenic loss, known to be significant for ^3He and ^(21)Ne, and to a lesser extent for ^(36)Ar (Signer et al. 1977), also occurs to a negligible extent for the heaviest noble gases Kr and Xe

A new all-metal induction furnace for noble gas extraction

A new all-metal induction furnace for extraction of all noble gases from pyroxenes, olivines, quartz or barites has been developed at CRPG. It differs in design from other induction furnaces in that the totality of the vacuum vessel is metallic and the induction coil, normally located outside the furnace, has been placed inside the vacuum vessel, with a special radio frequency power feedthrough welded onto a flange. The volume of the crucible is ≈ 15 cm^3 and permits fusion of samples with a mass of up to 1 g. Samples are packed into a metal foil, loaded into a carousel, baked out before analysis, and then sequentially dropped into the Ta-crucible. The low weight of the crucible (≈ 120 g) allows for short and efficient degassing cycles. When the furnace is pumped for the first time after samples loading, short cycles between 500 and 1800 °C at fast heating rates (≈ 400 °C·min^(−1)) are sufficient to achieve very low blanks. The durations of these cycles are range from 30 min for He to up to a few hours for Ne, Kr and Xe. Blanks of He, Kr and Xe (10 min heating durations) and Ne (20 min) in static vacuum are (1.6 ± 1.0) × 10^(−15) mol ^4He (T = 1750 °C), (5.8 ± 2.3) × 10^(−17) mol ^(20)Ne (T = 1500 °C), (2.1 ± 0.3) × 10^(−18) mol ^(84)Kr (T = 1700 °C) and (4.4 ± 0.4) × 10^(−18) mol ^(132)Xe (T = 1700 °C). Argon blanks have not yet been measured

A race against the clock: Constraining the timing of cometary bombardment relative to Earth's growth

Comets are considered a potential source of inner solar system volatiles, but the timing of this delivery relative to that of Earth's accretion is still poorly understood. Measurements of xenon isotopes in comet 67P/Churyumov-Gerasimenko revealed that comets partly contributed to the Earth's atmosphere. However, there is no conclusive evidence of a significant cometary component in the Earth's mantle. These geochemical constraints would favour a contribution of comets mainly occurring after the last stages of Earth's formation. Here, we evaluate whether dynamical simulations satisfy these constraints in the context of an Early Instability model. We perform dynamical simulations of the solar system, calculate the probability of collision between comets and Earth analogs component embryos through time and estimate the total cometary mass accreted in Earth analogs as a function of time. While our results are in excellent agreement with geochemical constraints, we also demonstrate that the contribution of comets on Earth might have been delayed with respect to the timing of the instability, due to a stochastic component of the bombardment. More importantly, we show that it is possible that enough cometary mass has been brought to Earth after it had finished forming so that the xenon constraint is not necessarily in conflict with an Early Instability scenario. However, it appears very likely that a few comets were delivered to Earth early in its accretion history, thus contributing to the mantle's budget. Finally, we compare the delivery of cometary material on Earth to Venus and Mars. These results emphasize the stochastic nature of the cometary bombardment in the inner solar system.Comment: 26 pages, 12 figure

Noble gases and stable isotopes track the origin and early evolution of the Venus atmosphere

The composition the atmosphere of Venus results from the integration of many processes entering into play over the entire geological history of the planet. Determining the elemental abundances and isotopic ratios of noble gases (He, Ne, Ar, Kr, Xe) and stable isotopes (H, C, N, O, S) in the Venus atmosphere is a high priority scientific target since it could open a window on the origin and early evolution of the entire planet. This chapter provides an overview of the existing dataset on noble gases and stable isotopes in the Venus atmosphere. The current state of knowledge on the origin and early and long-term evolution of the Venus atmosphere deduced from this dataset is summarized. A list of persistent and new unsolved scientific questions stemming from recent studies of planetary atmospheres (Venus, Earth and Mars) are described. Important mission requirements pertaining to the measurement of volatile elements in the atmosphere of Venus as well as potential technical difficulties are outlined.Comment: 40 pages, 10 figures, 1 tabl