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This work reviews the long-term evolution of the atmosphere of Venus, and modulation of its composition by interior/exterior cycling. The formation and evolution of Venus’s atmosphere, leading to contemporary surface conditions, remain hotly debated topics, and involve questions that tie into many disciplines. We explore these various inter-related mechanisms which shaped the evolution of the atmosphere, starting with the volatile sources and sinks. Going from the deep interior to the top of the atmosphere, we describe volcanic outgassing, surface-atmosphere interactions, and atmosphere escape. Furthermore, we address more complex aspects of the history of Venus, including the role of Late Accretion impacts, how magnetic field generation is tied into long-term evolution, and the implications of geochemical and geodynamical feedback cycles for atmospheric evolution. We highlight plausible end-member evolutionary pathways that Venus could have followed, from accretion to its present-day state, based on modeling and observations. In a first scenario, the planet was desiccated by atmospheric escape during the magma ocean phase. In a second scenario, Venus could have harbored surface liquid water for long periods of time, until its temperate climate was destabilized and it entered a runaway greenhouse phase. In a third scenario, Venus’s inefficient outgassing could have kept water inside the planet, where hydrogen was trapped in the core and the mantle was oxidized. We discuss existing evidence and future observations/missions required to refine our understanding of the planet’s history and of the complex feedback cycles between the interior, surface, and atmosphere that have been operating in the past, present or future of Venus.

Several geochemical tracers (S, C, O, Xe) underwent irreversible global changes during the Precambrian, and in particular during the Great Oxygenation Event (GOE), between the Archean and Proterozoïc eons [1]. Xenon is of particular interest as it presents a secular isotopic evolution during the Archean that ceased around the time of the GOE. In this regard Xe is somewhat analogous to mass-independent fractionation sulfur (MIF-S) in that it can be used to categorically identify Archean atmospheric components [2]. Xe isotopes in the modern atmosphere are strongly mass-dependent fractionated (MDF-Xe), with a depletion of the light isotopes relative to the heavy ones. There was a continuous Xe isotope evolution from primitive Xe to modern Xe that ceased between 2.6 and 1.8 Ga [2] and this evolution has been attributed to coupled H+-Xe+ escape to space [3].The purpose of this project is to document the Xe composition of the paleo-atmosphere trapped in well-dated hydrothermal quartz fluid inclusions with ages covering the Archean-Proterozoic transition to better constraint its link with the GOE.We have measured an isotopically fractionated Xe composition of 2.0 ± 1.8 ‰ relative to modern atmosphere at 2441 ± 1.6 Ma, in quartz vein from the Seidorechka sedimentary formation (Imandra-Varzuga Greenstone belt, Russia). A slightly younger sample from the Polisarka sedimentary formation (Imandra-Varzuga Greenstone belt, Russia) of 2434 ± 6.6 Ma does not record such fractionation and is indistinguishable from the modern atmospheric composition. A temporal link between the disappearance of the Xe isotopes fractionation and the MIF-S signature at the Archean-Proterozoic transition is clearly established for the Kola Craton. The mass-dependent evolution of Xe isotopes is the witness of a cumulative atmospheric process that may have played an important role in the oxidation of the Earth's surface [3], independently of biogenic O2 production that started long before the permanent rise of O2 in the atmosphere [4]. [1] Catling & Zahnle, 2020, Sciences Advances 6, eaax1420. [2] Avice et al., 2018, Geochimica et Cosmochimica Acta 232, 82-100 [3] Zahnle et al., 2019, Geochimica et Cosmochimica Acta 244, 56-85. [4] Lyons et al., 2014, Nature 506, 307-315.

Dynamic models of solar system evolution suggest that D-type asteroids formed beyond Saturn's orbit and represent invaluable witnesses of the prevailing conditions in the outer solar system. Here, we report a comprehensive petrographic and isotopic characterization of the carbonaceous chondrite Tarda, a recent fall recovered in the Moroccan Sahara. We show that Tarda shares strong similarities with the D-type-derived chondrite Tagish Lake, implying that Tarda represents a rare sample of D-type asteroids. Both Tarda and Tagish Lake are characterized by the presence of rare 16O-rich chondrules and chondrule fragments, high C/H ratios, and enrichments in deuterium, 15N, and 13C. By combining our results with literature data on carbonaceous chondrites related to C-type asteroids, we show that the outer solar system 4.56 Gy ago was characterized by large-scale oxygen isotopic homogeneities in (i) the water–ice grains accreted by asteroids and (ii) the gas controlling the formation of FeO-poor chondrules. Conversely, the zone in which D-type asteroids accreted was significantly enriched in deuterium relative to the formation regions of C-type asteroids, features likely inherited from unprocessed, D-rich, molecular-cloud materials.

Pressure maxima are regions in protoplanetary disks where pebbles can be trapped because of the local absence of pressure gradient. These regions could be ideal places to form planetesimals or to isolate isotopic reservoirs. Observations of protoplanetary disks show that dusty rings structures are common, and pressure maxima are sometime invoked as a possible explanation. In our Solar System, pressure bumps have been suggested as a possible mechanism for separating reservoirs with different nucleosynthetic compositions. In this letter we detail a mechanism by which pressure maxima form just inward the snow-line in stratified disks. This mechanism does not need the presence of a planet. Using a combination of analytical and numerical investigation we explore the range of conditions for a pressure maximum to form inside the dead-zone and just inward the snow-line. When the vertically averaged $��$ is a decreasing function of surface density then the release of water vapor at the snow-line lowers the sound velocity, and in turn, a pressure bump appears. This requires a constant inflow of icy pebbles with pebbles influx to gas influx $>0.6$ for a power law disk with $1\%$ ice/gas ratio, and $>1.8$ for a disk with ice/gas ratio $\sim 0.3\%$. If these conditions are met, then a Pressure-maximum appears just inward the snow-line due to a process coupling the dead and active layers at the evaporation front. The pressure bump survives as long as the icy pebble flux is high enough. The formation of the pressure bump is triggered by the drop of sound velocity inward the snow-line, due to the release of water vapor. This mechanism is promising for isolating early reservoirs carrying different isotopic signatures in the Solar System and for promoting dry planetesimal formation inward the snow-line, provided the vertically averaged description of a dead-zone is valid., 12 pages, 6 Figures, 1 Figures in Appendix, accepted for publication in Astronomy & Astrophysics (A&A)

International audience; Nitrogen is the main constituent of the Earth's atmosphere, but its provenance in the Earth's mantle remains uncertain. The relative contribution of primordial nitrogen inherited during the Earth's accretion versus that subducted from the Earth's surface is unclear 1-6. Here we show that the mantle may have retained remnants of such primordial nitrogen. We use the rare 15 N 15 N isotopologue of N 2 as a new tracer of air contamination in volcanic gas effusions. By constraining air contamination in gases from Iceland, Eifel (Germany) and Yellowstone (USA), we derive estimates of mantle δ 15 N (the fractional difference in 15 N/ 14 N from air), N 2 / 36 Ar and N 2 / 3 He. Our results show that negative δ 15 N values observed in gases, previously regarded as indicating a mantle origin for nitrogen 7-10 , in fact represent dominantly air-derived N 2 that experienced 15 N/ 14 N fractionation in hydrothermal systems. Using two-component mixing models to correct for this effect, the 15 N 15 N data allow extrapolations that characterize mantle endmember δ 15 N, N 2 / 36 Ar and N 2 / 3 He values. We show that the Eifel region has slightly increased δ 15 N and N 2 / 36 Ar values relative to estimates for the convective mantle provided by mid-ocean-ridge basalts 11 , consistent with subducted nitrogen being added to the mantle source. In contrast, we find that whereas the Yellowstone plume has δ 15 N values substantially greater than that of the convective mantle, resembling surface components 12-15 , its N 2 / 36 Ar and N 2 / 3 He ratios are indistinguishable from those of the convective mantle. This observation raises the possibility that the plume hosts a primordial component. We provide a test of the subduction hypothesis with a two-box model, describing the evolution of mantle and surface nitrogen through geological time. We show that the effect of subduction on the deep nitrogen cycle may be less important than has been suggested by previous investigations. We propose instead that high mid-ocean-ridge basalt and plume δ 15 N values may both be dominantly primordial features. Differentiated bodies from our Solar System have rocky mantles with 15 N/ 14 N ratios within ±15‰ of modern terrestrial air 16,17. This is true for Earth's convective mantle, which has a δ 15 N value of approximately −5 ± 3‰, based on measurements from diamonds 5,18 and basalts that have been filtered for air contamination 3,11. Conversely, volatile-rich chondritic meteorites exhibit highly variable δ 15 N values between −20 ± 11‰ for enstatite chondrites and 48 ± 9‰ for CI carbonaceous chondrites 16,19. The distinct 15 N/ 14 N of rocky mantles relative to the chon-drites may reflect inheritance of N from a heterogeneous mixture of chondritic precursors 3. Alternatively, the relatively high 15 N/ 14 N values could be the result of evaporative losses 20 , or equilibrium partitioning of N isotopes between metal cores and rocky mantles 21,22. For Earth, plate tectonics allows for another interpretation 1. Geo-chemists have suggested that mantle δ 15 N values reflect subduction of nitrogen from the surface. Some of the evidence comes from studies of gases from mantle plumes. On Earth, mantle plumes with high 3 He/ 4 He ratios relative to mid-ocean-ridge basalts (MORBs) result from melting of relatively undegassed portions of the deep mantle 23. Nitrogen data are sparse, but plumes with both high and low 3 He/ 4 He values have δ 15 N values between 0 and +3‰ (refs. 2,4), higher than the values attributed to the convective mantle and similar to both sediments and altered oceanic crust (Extended Data Fig. 1) 12,13,15,24. One hypothesis is that the convective and deep mantle reservoirs both initially had identical but low enstatite chondrite-like δ 15 N values 6. Over geological time, these

International audience; 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.

Here we discuss the current state of knowledge on how atmospheric escape processes can fractionate noble gas isotopes and moderately volatile rock-forming elements that populate primordial atmospheres, magma ocean related environments, and catastrophically outgassed steam atmospheres. Variations of isotopes and volatile elements in different planetary reservoirs keep information about atmospheric escape, composition and even the source of accreting material. We summarize our knowledge on atmospheric isotope ratios and discuss the latest evidence that proto-Venus and Earth captured small H$_2$-dominated primordial atmospheres that were lost by EUV-driven hydrodynamic escape after the disk dispersed. All relevant thermal and non-thermal atmospheric escape processes that can fractionate various isotopes and volatile elements are discussed. Erosion of early atmospheres, crust and mantle by large planetary impactors are also addressed. Further, we discuss how moderately volatile elements such as the radioactive heat producing element $^{40}$K and other rock-forming elements such as Mg can also be outgassed and lost from magma oceans that originate on large planetary embryos and accreting planets. Outgassed elements escape from planetary embryos with masses that are $\geq$\,M$_{\rm Moon}$ directly, or due to hydrodynamic drag of escaping H atoms originating from primordial- or steam atmospheres at more massive embryos. We discuss how these processes affect the final elemental composition and ratios such as K/U, Fe/Mg of early planets and their building blocks. Finally, we review modeling efforts that constrain the early evolution of Venus, Earth and Mars by reproducing their measured present day atmospheric $^{36}$Ar/$^{38}$Ar, $^{20}$Ne/$^{22}$Ne noble gas isotope ratios and the role of isotopes on the loss of water and its connection to the redox state on early Mars., Comment: 65 pages, 17 figures. This is a preprint of an article published in Space Science Reviews. The final authenticated version can be found online at: https://doi.org/10.1007/s11214-020-00701-x

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.

Measuring the abundance and isotopic composition of noble gases in planetary atmospheres can answer fundamental questions in cosmochemistry and comparative planetology. However, noble gases are rare elements, a feature making their measurement challenging even on Earth. Furthermore, in space applications, power consumption, volume and mass constraints on spacecraft instrument accommodations require the development of compact innovative instruments able to meet the engineering requirements of the mission while still meeting the science requirements. Here we demonstrate the ability of the quadrupole ion trap mass spectrometer (QITMS) developed at the Jet Propulsion Laboratory (Caltech, Pasadena) to measure low quantities of heavy noble gases (Kr, Xe) in static operating mode and in the absence of a buffer gas such as helium. The sensitivity reaches 1E13 cps Torr-1 (about 1011 cps/Pa) of gas (Kr or Xe). The instrument is able to measure gas in static mode for extended periods of time (up to 48 h) enabling the acquisition of thousands of isotope ratios per measurement. Errors on isotope ratios follow predictions of the counting statistics and the instrument provides reproducible results over several days of measurements. For example, 1.7E-10 Torr (2.3E-8 Pa) of Kr measured continuously for 7 hours yielded a 0.6 permil precision on the 86Kr/84Kr ratio. Measurements of terrestrial and extraterrestrial samples reproduce values from the literature. A compact instrument based upon the QITMS design would have a sensitivity high enough to reach the precision on isotope ratios (e.g. better than 1 percent for 129,131-136Xe/130Xe ratios) necessary for a scientific payload measuring noble gases collected in the Venus atmosphere., Comment: 42 pages, 9 figures, 4 tables

Nucleosynthetic isotopic anomalies in meteorites and planetary objects contribute to our understanding of the formation of the solar system. Isotope systematics of chondrites demonstrate the existence of a physical separation between isotopic reservoirs in the solar system. The isotopic composition of atmospheric xenon (Xe) indicates that its progenitor, U-Xe, is depleted in 134Xe and 136Xe isotopes relative to solar or chondritic end-members. This deficit supports the view that nucleosynthetic heterogeneities persisted during the solar system formation. Measurements of xenon emitted from comet 67P/Churyumov-Gerasimenko (67P) identified a similar, but more extreme, deficit of cometary gas in these isotopes relative to solar gas. Here we show that the data from 67P demonstrate that two distinct sources contributed xenon isotopes associated with the r-process to the solar system. The h-process contributed at least 29% (2σ) of solar system 136Xe. Mixtures of these r-process components and the s-process that match the heavy isotope signature of cometary Xe lead to depletions of the precursor of atmospheric Xe in p-only isotopes. Only the addition of pure p-process Xe to the isotopic mixture brings 124Xe/132Xe and 126Xe/132Xe ratios back to solar-like values. No pure p-process Xe has been detected in solar system material, and variation in p-process Xe isotopes is always correlated with variation in r-process Xe isotopes. In the solar system, p-process incorporation from the interstellar medium happened before incorporation of r-process nuclides or material in the outer edge of the solar system carries a different mixture of presolar sources as have been preserved in parent bodies.

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.

The main carrier of primordial heavy noble gases in chondrites is thought to be an organic phase, known as phase Q, whose precise characterization has resisted decades of investigation. Indirect techniques have revealed that phase Q might be composed of two subphases, one of them associated with sulfide. Here we provide experimental evidence that noble gases trapped within meteoritic sulfides present chemically- and thermally-driven behavior patterns that are similar to Q-gases. We therefore suggest that phase Q is likely composed of two subcomponents: carbonaceous phases and sulfides. In situ decay of iodine at concentrations levels consistent with those reported for meteoritic sulfides can reproduce the 129Xe excess observed for Q-gases relative to fractionated Solar Wind. We suggest that the Q-bearing sulfides formed at high temperature and could have recorded the conditions that prevailed in the chondrule-forming region(s).

International audience; This is a follow-up study of a work by Kramers et al. (2013) on a very unusual diamond-rich rock fragment found in the area of south west Egypt in the south-western side of the Libyan Desert Glass strewn field. This pebble, called Hypatia, is composed of almost pure carbon. Transmission Electron Microscopy (TEM) and X-ray diffraction (XRD) results reveal that Hypatia is mainly made of defect-rich diamond containing lonsdaleite and multipledeformation bands. These characteristics are compatible with an impact origin on Earth and/or in space. We also analyzed concentrations and isotopic compositions of all five noble gases and nitrogen in several ~mg sized Hypatia samples. These data confirm the conclusion by Kramers et al. (2013) that Hypatia is extra-terrestrial. The sample is relatively rich in trapped noble gases with an isotopic composition being close to the Q component found in many types of meteorites. 40Ar/36Ar ratios in individual steps are as low as 0.4 ± 0.3. Cosmicray produced "cosmogenic" 21Ne is present in concentrations corresponding to a nominal cosmic-ray exposure (CRE) age of roughly 0.1 Myr if produced in a typical meter-sized meteoroid. Such an atypically low nominal CRE age suggests high shielding in a considerably larger body. In addition to the Xe-Q composition, an excess of radiogenic 129Xe (from thedecay of short-lived radioactive 129I) is observed (129Xe/132Xe = 1.18 +/- 0.03). Two isotopically distinct N components are present, an isotopically heavy component (δ15N ~ +20‰) released at low temperatures and a major isotopically light component (δ15N ~ -10‰) at higher temperatures. This disequilibrium in N suggests that the diamonds in Hypatia were formed in space rather than upon impact on Earth (δ15Natm = 0 ‰). All our dataare broadly consistent with concentrations and isotopic compositions of noble gases in at least three different types of carbon-rich meteoritic materials: carbon-rich veins in ureilites, graphite in acapulcoites/lodranites and graphite nodules in iron meteorites. However, Hypatia does not seem to be directly related to any of these materials, but may have sampled a similar cosmochemical reservoir. Our study does not confirm the presence of exotic noble gases (e.g. G component) that led Kramers et al. (2013) to propose that Hypatia is a remnant of a comet nucleus that impacted the Earth.

We report a systematic oxygen isotopic survey of Ca-carbonates in nine different CM chondrites characterized by different degrees of alteration, from the least altered known to date (Paris, 2.7–2.8) to the most altered (ALH 88045, CM1). Our data define a continuous trend that crosses the Terrestrial Fractionation Line (TFL), with a general relationship that is indistinguishable within errors from the trend defined by both matrix phyllosilicates and bulk O-isotopic compositions of CM chondrites. This bulk-matrix-carbonate (BMC) trend does not correspond to a mass-dependent fractionation (i.e., slope 0.52) as it would be expected during fluid circulation along a temperature gradient. It is instead a direct proxy of the degree of O-isotopic equilibration between 17,18O-rich fluids and 16O-rich anhydrous minerals. Our O-isotopic survey revealed that, for a given CM, no carbonate is in O-isotopic equilibrium with its respective surrounding matrix. This precludes direct calculation of the temperature of carbonate precipitation. However, the O-isotopic compositions of alteration water in different CMs (inferred from isotopic mass-balance calculation and direct measurements) define another trend (CMW for CM Water), parallel to BMC but with a different intercept. The distance between the BMC and CMW trends is directly related to the temperature of CM alteration and corresponds to average carbonates and serpentine formation temperatures of 110 °C and 75 °C, respectively. However, carbonate O-isotopic variations around the BMC trend indicate that they formed at various temperatures ranging between 50 and 300 °C, with 50% of the carbonates studied here showing precipitation temperature higher than 100 °C. The average Δ17O and the average carbonate precipitation temperature per chondrite are correlated, revealing that all CMs underwent similar maximum temperature peaks, but that altered CMs experienced protracted carbonate precipitation event(s) at lower temperatures than the least altered CMs. Our data suggest that the Δ17O value of Ca-carbonates could be a reliable proxy of the degree of alteration experienced by CM chondrites.

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

International audience; Noble gas isotopes are powerful tracers of the origins of planetary volatiles, and the accretion and evolution of the Earth. The compositions of magmatic gases provide insights into the evolution of the Earth’s mantle and atmosphere. Despite recent analytical progress in the study of planetary materials and mantle-derived gases, the possible dual origin of the planetary gases in the mantle and the atmosphere remains unconstrained. Evidence relating to the relationship between the volatiles within our planet and the potential cosmochemical end-members is scarce5. Here we show, using high-precision analysis of magmatic gas from the Eifel volcanic area (in Germany), that the light xenon isotopes identify a chondritic primordial component that differs from the precursor of atmospheric xenon. This is consistent with an asteroidal origin for the volatiles in the Earth’s mantle, and indicates that the volatiles in the atmosphere and mantle originated from distinct cosmochemical sources. Furthermore, our data are consistent with the origin of Eifel magmatism being a deep mantle plume. The corresponding mantle source has been isolated from the convective mantle since about 4.45 billion years ago, in agreement with models that predict the early isolation of mantle domains. Xenon isotope systematics support a clear distinction between mid-ocean-ridge and continental or oceanic plume sources6, with chemical heterogeneities dating back to the Earth’s accretion. The deep reservoir now sampled by the Eifel gas had a lower volatile/refractory (iodine/plutonium) composition than the shallower mantle sampled by mid-ocean-ridge volcanism, highlighting the increasing contribution of volatile-rich material during the first tens of millions of years of terrestrial accretion.

International audience; Recent measurements of the volatile composition of the coma of Comet 67P/Churyumov-Gerasimenko (hereafter 67P) allow constraints to be set on the origin of volatile elements (water, carbon, nitrogen, noble gases) in inner planets' atmospheres. Analyses by the ROSINA mass spectrometry system onboard the Rosetta spacecraft indicate that 67P ice has a D/H ratio three times that of the ocean value (Altwegg et al., 2015) and contains significant amounts of N2, CO, CO2, and importantly, argon (Balsiger et al., 2015). Here we establish a model composition of cometary composition based on literature data and the ROSINA measurements. From mass balance calculations, and provided that 67P is representative of the cometary ice reservoir, we conclude that the contribution of cometary volatiles to the Earth's inventory was minor for water (≤ 1%), carbon (≤ 1%), and nitrogen species (a few % at most). However, cometary contributions to the terrestrial atmosphere may have been significant for the noble gases. They could have taken place towards the end of the main building stages of the Earth, after the Moon-forming impact and during either a late veneer episode or, more probably, the Terrestrial Late Heavy Bombardment around 4.0-3.8 billion years (Ga) ago. Contributions from the outer solar system via cometary bodies could account for the dichotomy of the noble gas isotope compositions, in particular xenon, between the mantle and the atmosphere. A mass balance based on 36Ar and organics suggests that the amount of prebiotic material delivered by comets could have been quite considerable – equivalent to the present-day mass of the biosphere. On Mars, several of the isotopic signatures of surface volatiles (notably the high D/H ratios) are clearly indicative of atmospheric escape processes. Nevertheless, we suggest that cometary contributions after the major atmospheric escape events, e.g., during a Martian Late Heavy Bombardment towards the end of the Noachian era, could account for the Martian elemental C/N/36Ar ratios, solar-like krypton isotope composition and high 15N/14N ratios. Taken together, these observations are consistent with the volatiles of Earth and Mars being trapped initially from the nebular gas and local accreting material, then progressively added to by contributions from wet bodies from increasing heliocentric distances. Overall, no unified scenario can account for all of the characteristics of the inner planet atmospheres. Advances in this domain will require precise analysis of the elemental and isotopic compositions of comets and therefore await a cometary sample return mission.

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 tables

A New Rock from Mars On 18 July 2011 a meteorite originating from Mars fell on the moroccan desert. Chennaoui Aoudjehane et al. (p. 785 , published online 11 October) show that this meteorite was ejected from the surface of Mars 700,000 years ago and contains components derived from the interior, surface, and atmosphere of the red planet. Previous to this fall, only four other martian meteorites have been collected after being witnessed falling to Earth. All the other martian meteorites that are represented in collections around the world, have been found long after their arrival on Earth, and thus have suffered from exposure to the terrestrial environment.