Incorporation of argon, krypton and xenon into clathrates on Mars

Calculations of the trapping of heavy noble gases within multiple guest clathrates under Mars-like conditions show that a substantial fraction of the martian Xe, perhaps even the vast majority, could be in clathrates. In addition, the Xe/Kr ratio in the clathrates would probably be much higher than in the atmosphere, so the formation or dissociation of a relatively small amount of clathrate could measurably change the atmospheric ratio. Relatively crude (factor of 2) measurements of the seasonal variability in that ratio by in situ spacecraft would be sensitive to ∼10% of the seasonal atmospheric CO₂ variability being a result of clathrates, rather than pure CO₂ frost. In addition, sequestration of Xe in clathrates remains a viable mechanism for explaining the variable Xe/Kr ratios seen in different suites of martian meteorites.     

Trapping of noble gases in proton-irradiated silicate smokes

Abstract— We have measured Ne, Ar, Kr and Xe in Si₂O₃ “smokes” that were condensed on Al substrates, vapor-deposited with various mixtures of CH₄, NH₃, H₂O and noble gases at 10 K and subsequently irradiated with 1 MeV protons to simulate conditions during grain mantle formation in interstellar clouds. The noble gases were analyzed using conventional stepwise heating and static noble gas mass spectrometry. Neither Ne nor Ar is retained by the samples upon warming to room temperature, but Xe is very efficiently trapped and retained. Kr is somewhat less effectively retained, typically depleted by factors of about 10–20 relative to Xe. Isotopic fractionation favoring the heavy isotopes of Xe and Kr of about 5–10‰/amu is observed. Correlations between the specific chemistry of the vapor deposition and heavy noble gas retention are most likely the result of competition by the various species for irradiation-produced trapping sites. The concentration of Xe retained by some of these smokes exceeds that observed in phase Q of meteorites and, like phase Q, they do not seem to be carriers of the light noble gases. Such artificially prepared material may, therefore, offer clues concerning the incorporation of the heavy planetary noble gases in meteoritic material and the nature of phase Q.     

Ice clathrate as a possible source of the atmospheres of the terrestrial planets

The presence and compositions of atmospheres on the terrestrial planets do not follow directly from condensation models which would have Earth accreting near 500°K. No single mechanism yet proposed adequately accounts for the abundances of noble gases and carbon and nitrogen in the atmospheres. We show that the composition of clathrates forming at low temperatures in cold regions of the nebula can be predicted. Addition of about 1 ppm clathrate material to the Earth can explain observed abundances of Ar, Kr, and Xe. Condensation and adsorption processes occuring at 400–500°K are necessary to explain the observed abundances of Ne, H₂O, C, and N. Possible sources of clathrates could be cometary bodies formed in the outer solar system.     

Krypton and xenon fractionation in North American tektites

Abstract— Elemental and isotopic compositions of the noble gases have been determined in six North American tektites (4 bediasites and 2 georgiaites) and one Ivory Coast tektite. Radiogenically produced ⁴He may explain the large ⁴He/³⁶Ar ratios measured relative to air, despite significant diffusive losses. The Ne isotopic composition is enriched in ²⁰Ne consistent with a single stage mass fractionation process. The enormous ²⁰Ne/³⁶Ar enrichments observed in all tektite samples, similar to those reported from other tektites and impact glasses, are attributed to atmospheric diffusion into the samples following solidification. The North American tektites show a systematic increase in ⁸⁴Kr/³⁶Ar and ¹³²Xe/³⁶Ar relative to air, with enrichments greater than those determined for any other tektite group or terrestrial samples other than shales. These enrichments are inconsistent with existing models of dissolving Kr and Xe in tektite glass without elemental fractionation at atmospheric pressures equivalent to ∼40 km altitude. The Kr and Xe isotopic compositions are indistinguishable from atmospheric within experimental uncertainty.     

Noble gases in enstatite chondrites II: The trapped component

Abstract— The trapped noble gas record of 57 enstatite chondrites (E chondrites) has been investigated. Basically, two different gas patterns have been identified dependent on the petrologic type. All E chondrites of type 4 to 6 show a mixture of trapped common chondritic rare gases (Q) and a subsolar component (range of elemental ratios for E4–6 chondrites: ³⁶Ar/¹³²Xe = 582 ± 270 and ³⁶Ar/⁸⁴Kr = 242 ± 88). E3 chondrites usually contain Q gases, but also a composition with lower ³⁶Ar/¹³²Xe and ³⁶Ar/⁸⁴Kr ratios, which we call sub‐Q (³⁶Ar/¹³²Xe = 37.0 ± 18.0 and ³⁶Ar/⁸⁴Kr = 41.7 ± 18.1). The presence of either the subsolar or the sub‐Q signature in particular petrologic types cannot be readily explained by parent body metamorphism as postulated for ordinary chondrites. We therefore present a different model that can explain the bimodal distribution and composition of trapped heavy noble gases in E chondrites. Trapped solar noble gases have been observed only in some E3 chondrites. About 30% of each group, EH3 and EL3 chondrites, amounting to 9% of all analyzed E chondrites show the solar signature. Notably, only one of those meteorites has been explicitly described as a regolith breccia.     

Atmospheric Losses Under Dust Bombardment in the Ancient Atmospheres

We have considered the new process of atmospheric losses - “sputtering” under bombardment by interplanetary dust. It is demonstrated that “sputtering” due to collisions with the interplanetary dust is an effective way of atmospheric gas loss (10^–4–10^–3 of the dust particles' accreting mass) and that it changes the composition of the atmospheric gases. In calculations we have taken that the dust particles collide elastically with the atoms and molecules of the atmosphere. Estimation of the effects of inelastic collisions was also considered. As a result of these collisions a part of the atmospheric atoms and molecules will have “upward” velocity and enough energy to escape. It was considered that escaping atoms can collide with the atoms of the “main” gas of the upper atmosphere. The atmospheric gas composition is assumed to be just as in the modern Martian atmosphere - the “main” gases in the upper atmosphere were taken to be O and CO₂. In our computations we pay particular attention to the abundance of noble gases in planetary atmospheres since these gases are very important for theories of atmospheric origin. We computed that under “sputtering” by the interplanetary dust, atmospheres were enriched by the “heavy” elements and isotopes in the wide range of the upper atmospheric parameters O/CO₂, T/g (O/CO₂– on the level of homosphere;T is temperature of the exosphere,g is gravitational acceleration). However the loss efficiency for “heavy” gases is relatively high compared to other known gas loss processes. In the case of noble gases for the specific parameters of the upper atmosphere (small T/g ratio; high O/CO₂ on the level of homosphere) we have got the unique result: despite the diffusion separation in the upper atmosphere the loss efficiency of Xe > Kr > Ar. The effect of “sputtering” of the planetary atmospheres was strongest during the early stages of the planetary evolution - when the rate of the dust accretion was intrinsically higher than now because of collisions of planetesimals. In light of the new escape process, the main peculiarities of the noble gases abundance in the planetary atmospheres could be explained. This revised version was published online in July 2006 with corrections to the Cover Date.     

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 CO₂ 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 ²¹Ne, ³⁸Ar, ⁸³Kr, and ¹²⁶Xe, 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 ²¹Ne, and to a lesser extent for ³⁶Ar (Signer et al. 1977 ), also occurs to a negligible extent for the heaviest noble gases Kr and Xe.     

Isotopic composition of trapped and cosmogenic noble gases in several Martian meteorites

Abstract— Isotopic abundances of the noble gases were measured in the following Martian meteorites: two shock glass inclusions from Elephant Moraine (EET) 79001, shock vein glass from Shergotty and Yamato (Y) 793605, and whole-rock samples of Allan Hills (ALH) 84001 and Queen Alexandra Range (QUE) 94201. These glass samples, when combined with literature data on a separate single glass inclusion from EET 79001 and a glass vein from Zagami, permit examination in greater detail of the isotopic composition of Ne, Ar, Kr, and Xe trapped from the Martian atmosphere. The isotopic composition of Martian Ne, if actually present in these glasses, remains poorly defined. The ⁴⁰Ar/³⁶Ar ratio of trapped Martian atmospheric Ar is probably considerably lower than the nominal ratio of 3000 measured by Viking, and data on impact glasses suggest a value of ～1900. The atmospheric ³⁶Ar/³⁸Ar ratio is ≤4.0. Martian atmospheric Kr may be enriched in lighter isotopes by ～0.5%/amu compared to both solar-wind Kr and to the Martian composition previously reported. The isotopic composition of Xe in these glasses agrees with that previously reported in the literature. The Martian atmospheric ³⁶Ar/¹³²Xe and ⁸⁴Kr/¹³²Xe elemental ratios are higher than those reported by Viking by factors of ～2.5–1.6 (depending on the ⁴⁰Ar/³⁶Ar ratio adopted) and ～1.8, respectively, and are discussed in a separate paper. Cosmogenic gases indicate space exposure ages of 2.7 ± 0.6 Ma for QUE 94201 and Shergotty and 14 ± 1 Ma for ALH 84001. Small amounts of ²¹Ne produced by energetic solar protons may be present in QUE 94201 but are not present in ALH 84001 or Y-793605. The space exposure age for Y-793605 is 4.9 ± 0.6 Ma and appears to be distinctly older than the ages for basaltic shergottites. However, uncertainties in cosmogenic production rates still makes somewhat uncertain the number of Martian impact events required to produce the exposure ages of Martian meteorites.     

Rumuruti chondrites: Noble gases,exposure ages,pairing, and parent body history

Abstract— In this paper, we present concentration and isotopic composition of the light noble gases He, Ne, and Ar as well as of ⁸⁴Kr, ¹³²Xe, and ¹²⁹Xe in bulk samples of 33 Rumuruti (R) chondrites. Together with previously published data of six R chondrites, exposure ages are calculated and compared with those of ordinary chondrites. A number of pairings, especially between those from Northwest Africa (NWA), are suggested, so that only 23 individual falls are represented by the 39 R chondrites discussed here. Eleven of these meteorites, or almost 50%, contain solar gases and are thus regolithic breccias. This percentage is higher than that of ordinary chondrites, howardites, or aubrites. This may imply that the parent body of R chondrites has a relatively thick regolith. Concentrations of heavy noble gases, especially of Kr, are affected by the terrestrial atmospheric component, which resides in weathering products. Compared to ordinary chondrites, ¹²⁹Xe/¹³²Xe ratios of R chondrites are high.     

Primordial noble gases in “phase Q” in carbonaceous and ordinary chondrites studied by closed‐system stepped etching

Abstract— The HF/HCI‐resistant residues of the chondrites CM2 Cold Bokkeveld, CV3 (ox.) Grosnaja, CO3.4 Lancé, CO3.7 Isna, LL3.4 Chainpur, and H3.7 Dimmitt have been measured by closed‐system stepped etching (CSSE) in order to better characterise the noble gases in “phase Q”, a major carrier of primordial noble gases. All isotopic ratios in phase Q of the different meteorites are quite uniform, except for (²⁰Ne/²²Ne)_Q. As already suggested by precise earlier measurements (Schelhaas et al., 1990; Wieler et al., 1991, 1992), (²⁰Ne/²²Ne)_Q is the least uniform isotopic ratio of the Q noble gases. The data cluster ～10.1 for Cold Bokkeveld and Lancé and 10.7 for Chainpur, Grosnaja, and Dimmitt, respectively. No correlation of (²⁰Ne/²²Ne)_Q with the classification or the alteration history of the meteorites has been found. The Ar, Kr, and Xe isotopic ratios for all six samples are identical within their uncertainties and similar to earlier Q determinations as well as to Ar‐Xe in ureilites. Thus, an unknown process probably accounts for the alteration of the originally incorporated Ne‐Q. The noble gas elemental compositions provide evidence that Q consists of at least two carbonaceous carrier phases “Q1” and “Q2” with slightly distinct chemical properties. Ratios (Ar/Xe)_Q and (Kr/Xe)_Q reflect both thermal metamorphism and aqueous alteration. These parent‐body processes have led to larger depletions of Ar and Kr relative to Xe. In contrast, meteorites that suffered severe aqueous alteration, such as the CM chondrites, do not show depletions of He and Ne relative to Ar but rather the highest (He/Ar)_Q and (Ne/Ar)_Q ratios. This suggests that Q1 is less susceptible to aqueous alteration than Q₂. Both subphases may well have incorporated noble gases from the same reservoir, as indicated by the nearly constant, though very large, depletion of the lighter noble gases relative to solar abundances. However, the elemental ratios show that Q₁ and Q₂ must have acquired (or lost) noble gases in slightly different element proportions. Cold Bokkeveld suggests that Q₁ may be related to presolar graphite. Phases Q₁ and Q₂ might be related to the subphases that have been suggested by Gros and Anders (1977). The distribution of the ²⁰Ne/²²Ne ratios cannot be attributed to the carriers Q₁ and Q₂. The residues of Chainpur and Cold Bokkeveld contain significant amounts of Ne‐E(L), and the data confirm the suggestion of Huss (1997) that the ²²Ne‐E(L) content, and thus the presolar graphite abundances, are correlated with the metamorphic history of the meteorites.     

Noble gases in planetary atmospheres: Implications for the origin and evolution of atmospheres

The radiogenic and primordial noble gas content of the atmospheres of Venus, Earth, and Mars are compared with one another and with the noble gas content of other extraterrestial samples, especially meteorites. The fourfold depletion of ⁴⁰Ar for Venus relative to the Earth is attributed to the outgassing rates and associated tectonics and volcanic styles for the two planets diverging significantly within the first billion or so years of their history, with the outgassing rate for Venus becoming much less than that for the Earth at subsequent times. This early divergence in the tectonic style of the two planets may be due to a corresponding early onset of the runaway greenhouse on Venus. The 16-fold depletion of ⁴⁰Ar for Mars relative to the Earth may be due to a combination of a mild K depletion for Mars, a smaller fraction of its interior being outgassed, and to an early reduction in its outgassing rate. Venus has lost virtually all of its primordial He and some of its radiogenic He. The escape flux of He may have been quite substantial in Venus' early history, but much diminished at later times, with this time variation being perhaps strongly influenced by massive losses of H₂ resulting from efficient H₂O loss processes.Key trends in the primordial noble gas content of terrestial planetary atmospheres include (1) a several orders of magnitude decrease in ²⁰Ne and ³⁶Ar from Venus to Earth to Mars; (2) a nearly constant ²⁰Ne/³⁶Ar ratio which is comparable to that found in the more primitive carbonaceous chondrites and which is two orders of magnitude smaller than the solar ratio; (3) a sizable fractionation of Ar, Kr, and Xe from their solar ratios, although the degree of fractionation, especially for ³⁶Ar/¹³²Xe, seems to decrease systematically from carbonaceous chondrites to Mars to Earth to Venus; and (4) large differences in Ne and Xe isotopic ratios among Earth, meteorites, and the Sun. Explaining trends (2), (2) and (4), and (1) pose the biggest problems for the solar-wind implantation, primitive atmosphere, and late veneer hypotheses, respectively. It is suggested that the grain-accretion hypothesis can explain all four trends, although the assumptions needed to achieve this agreement are far from proven. In particular, trends (1), (2), (3), and (4) are attributed to large pressure but small temperature differences in various regions of the inner solar system at the times of noble gas incorporation by host phases; similar proportions of the host phases that incorporated most of the He and Ne on the one hand (X) and Ar, Kr, and Xe on the other hand (Q); a decrease in the degree of fractionation with increasing noble-gas partial pressure; and the presence of interstellar carriers containing isotopically anomalous noble gases.Our analysis also suggests that primordial noble gases were incorporated throughout the interior of the outer terrestial planets, i.e., homogeneous accretion is favored over inhomogeneous accretion. In accord with meteorite data, we propose that carbonaceous materials were key hosts for the primordial noble gases incorporated into planets and that they provided a major source of the planets' CO₂ and N₂.     

81Kr‐Kr age and multiple cosmic‐ray exposure history of the Vaca Muerta mesosiderite

Abstract– Noble gas isotopic compositions were measured for a eucritic pebble and bulk material of a silicate–metal mixture from the Vaca Muerta mesosiderite as well as pyroxene and plagioclase separated from the eucritic pebble by total melting and stepwise heating methods. Trapped noble gases were degassed completely by a high‐temperature thermal event, probably at the formation of the Vaca Muerta parent body (VMPB). The presence of fissiogenic Xe isotopes from extinct ²⁴⁴Pu in the bulk samples might be a result of rapid cooling from an early high‐temperature metamorphism. High concentrations of cosmogenic noble gases enabled us to determine precise isotopic ratios of cosmogenic Kr and Xe. Spallogenic Ne from Na and unique Ar isotopic compositions were observed. The ⁸¹Kr‐Kr exposure age of 168 ± 8 Myr for the silicate pebble is distinctly longer than the age of 139 ± 8 Myr for the bulk samples. The precursor of the pebble had been irradiated on the surface of the VMPB for more than 60 Myr (first stage irradiation), with subsequent incorporation into bulk materials approximately 4 Gyr ago. The Vaca Muerta meteorite was excavated from the VMPB 140 Myr ago (second stage irradiation). Relative diffusion rates among the cosmogenic Ar, Kr, and Xe based on data obtained by stepwise heating indicate that Kr and Xe can be partially retained in pyroxene and plagioclase under the condition that resets the K‐Ar system. This result supports the presence of fission Xe and of excess concentration of cosmogenic Kr, which could have survived the thermal event approximately 3.8 Gyr ago.     

Noble gas compositions of Antarctic micrometeorites collected at the Dome Fuji Station in 1996 and 1997

Abstract— The noble gases He, Ne, Ar, Kr, and Xe were measured in 27 individual Antarctic micrometeorites (AMMs) in the size range 60 to 250 μm that were collected at the Dome Fuji Station. Eleven of the AMMs were collected in 1996 (F96 series) and 16 were collected in 1997 (F97 series). One of the F97 AMMs is a totally melted spherule, whereas all other particles are irregular in shape. Noble gases were extracted using a Nd‐YAG continuous wave laser with an output power of 2.5‐3.5 W for ?5 min. Most particles released measurable amounts of noble gases. ³He/⁴He ratios are determined for 26 AMMs ((0.85‐9.65) × 10^?4). Solar energetic particles (SEP) are the dominant source of helium in most AMMs rather than solar wind (SW) and cosmogenic He. Three samples had higher ³He/⁴He ratios compared to that of SW, showing the presence of spallogenic ³He. The Ne isotopic composition of most AMMs resembled that of SEP as in the case of helium. Spallogenic ²¹Ne was detected in three samples, two of which had extremely long cosmic‐ray exposure ages (> 100 Ma), calculated by assuming solar cosmic‐ray (SCR) + galactic cosmic‐ray (GCR) production. These two particles may have come to Earth directly from the Kuiper Belt. Most AMMs had negligible amounts of cosmogenic ²¹ Ne and exposure ages of <1 Ma. ⁴⁰Ar/³⁶Ar ratios for all particles (3.9–289) were lower than that of the terrestrial atmosphere (296), indicating an extraterrestrial origin of part of the Ar with a very low ⁴⁰Ar/³⁶Ar ratio plus some atmospheric contamination. Indeed, ⁴⁰Ar/³⁶Ar ratios for the AMMs are higher than SW, SEP, and Q‐Ar values, which is explained by the presence of atmospheric ⁴⁰Ar. The average ³⁸Ar/³⁶Ar ratio of 24 AMMs (0.194) is slightly higher than the value of atmospheric or Q‐Ar, suggesting the presence of SEP‐Ar which has a relatively high ³⁸Ar/³⁶Ar ratio. According to the elemental compositions of the heavy noble gases, Dome Fuji AMMs can be classified into three groups: chondritic (eight particles), air‐affected (nine particles), and solar‐affected (eight particles). The eight AMMs classified as chondritic preserve the heavy noble gas composition of primordial trapped component due to lack of atmospheric adsorption and solar implantation. The average of ¹²⁹Xe/¹³²Xe ratio for the 16 AMMs not affected by atmospheric contamination (1.05) corresponds to the values in matrices of carbonaceous chondrites (?1.04). One AMM, F96DK038, has high ¹²⁹Xe/¹³²Xe in excess of this ratio. Our results imply that most Dome Fuji AMMs originally had chondritic heavy noble gas compositions, and carbonaceous chondrite‐like objects are appropriate candidate sources for most AMMs.     

Devgaon (H3) chondrite: Classification and complex cosmic ray exposure history

Abstract— The Devgaon meteorite fell in India on February 12, 2001 and was immediately collected. It is an ordinary chondrite having a number of SiO₂‐rich objects and some Ca, Al‐rich inclusions. Olivines (Fa_17–19) are fairly equilibrated, while pyroxenes (Fs_4–20) are unequilibrated. Occasionally, shock veins are visible, but the bulk rock sample is very weakly shocked (S2). Chondrules and chondrule fragments are abundant. Based on chemical and petrological features, Devgaon is classified as an H3.8 group chondrite. Several cosmogenic radionuclides ranging in half‐lives from 5.6 d (⁵²Mn) to 7.3 times 10⁵ yr (²⁶Al), noble gases (He, Ne, Ar, Kr, and Xe), and particle track density have been measured. The track density in olivines from five spot samples varies between (4.6 to 9) × 10⁶ cm^?2 showing a small gradient within the meteorite. The light noble gases are dominated by cosmogenic and radiogenic components. Large amounts of trapped gases (Ar, Kr, and Xe) are present. In addition, (n, γ) products from Br and I are found in Kr and Xe, respectively. The average cosmic ray exposure age of 101 ± 8 Ma is derived based on cosmogenic ³⁸Ar, ⁸³Kr, and ¹²⁶Xe. The track production rates correspond to shielding depths of about 4.9 to 7.8 cm, indicating that the stone suffered type IV ablation. Low ⁶⁰Co, high (²²Ne/²¹Ne)_c, and large neutron produced excesses at ⁸⁰Kr, ⁸²Kr, and ¹²⁸Xe indicate a complex exposure history of the meteoroid. In the first stage, a meter‐sized body was exposed for nearly 10⁸ yr in the interplanetary space that broke up in ?50 cm‐sized fragments about a million years ago (stage 2), before it was captured by the Earth.     

Noble gases in iddingsite from the Lafayette meteorite: Evidence for liquid water on Mars in the last few hundred million years

Abstract— We analyzed noble gases from 18 samples of weathering products (“iddingsite”) from the Lafayette meteorite. Potassium‐argon ages of 12 samples range from near zero to 670 ± 91 Ma. These ages confirm the martian origin of the iddingsite, but it is not clear whether any or all of the ages represent iddingsite formation as opposed to later alteration or incorporation of martian atmospheric ⁴⁰Ar. In any case, because iddingsite formation requires liquid water, this data requires the presence of liquid water near the surface of Mars at least as recently as 1300 Ma ago, and probably as recently as 650 Ma ago. Krypton and Xe analysis of a single 34 μg sample indicates the presence of fractionated martian atmosphere within the iddingsite. This also confirms the martian origin of the iddingsite. The mechanism of incorporation could either be through interaction with liquid water during iddingsite formation or a result of shock implantation of adsorbed atmospheric gas. Our strongest conclusion is that the iddingsite in Lafayette formed on Mars, in agreement with the microstratigraphic arguments of Gooding et al. (1991) and Treiman et al. (1993). A preterrestrial origin of the iddingsite is required both by the many non‐zero K‐Ar ages and by the presence of Xe that is isotopically distinct from any terrestrial Xe. The Xe is accompanied by Kr, but the Kr and Xe have been fractionated if they are derived from the present martian atmosphere. This is presumably the result of either incorporation via interaction with liquid water (Drake et al., 1994; Bogard and Garrison, 1998) or by adsorption from the martian atmosphere, perhaps accompanied by shock (see also Gilmour et al., 1998, 1999). Although the iddingsite is enriched in Kr and Xe compared to whole‐rock analyses, it is not clear whether iddingsite is the dominant carrier of the atmospheric‐derived gas (Drake et al., 1994) or merely a minor carrier (Gilmour et al., 1999). Our ⁴⁰Ar‐³⁹Ar experiment was disappointing, in that it mostly served to confirm that the iddingsite, which contains fine‐grained clays, is susceptible to recoil loss of ³⁹Ar during irradiation. Only one sample of five gave a clear signal of radiogenic or extraterrestrial ⁴⁰Ar, and that was only by 3°. Potassium‐argon ages of the second set of samples were more successful, ranging from near 0 to 670 ± 91 Ma. It is not clear whether any or all of the ages represent iddingsite formation, as opposed to later alteration. The fact that a Rb‐Sr experiment (Shih et al., 1998) gave an apparent age for iddingsite of 679 ± 66 Ma (2a) suggests that perhaps formation of iddingsite occurred (or began) ～650 Ma ago and that some samples either formed, or were thermally altered, later. The ages could be even younger than 650 Ma, if the samples have incorporated martian atmospheric ⁴⁰Ar. This means that liquid water was certainly present on Mars in the last 1300 Ma (the formation age of Lafayette), and probably within the last 650 Ma.     

Orphan radiogenic noble gases in lunar breccias: evidence for planet pollution of the Sun?

Surface-correlated noble gases in lunar soils are primarily implanted SW (solar wind) noble gases. However, they also include apparently orphan radiogenic ⁴⁰Ar, ¹²⁹Xe, and ²⁴⁴Pu-derived fission Xe in excess of plausible primordial solar origin. These orphan radiogenic components are usually assigned a lunar origin, in a scenario in which radiogenic noble gases produced in the lunar interior were degassed into the transient atmosphere and then re-implanted to the lunar surface together with SW. There are some quantitative difficulties with this scenario, however, and it requires special constraints on the degassing history of the Moon that have not emerged from more general thermal history models. We therefore urge consideration of alternative hypotheses. As a possible source for the orphan radiogenic noble gases, we have examined planetary pollution of the Sun, as suggested by studies of extrasolar planetary systems (e.g., Murray et al., 2001, Astrophys. J. 555, 801-815; Israelian et al., 2001, Nature 411, 163-166). Pollution of the Sun by 2M_⊕ (two Earth mass) planetary materials (Murray et al., 2001, Astrophys. J. 555, 801-815) is likely not significant for Ar but could be important to account for orphan Xe in the Moon.     

The dual origin of the terrestrial atmosphere

The origin of the terrestrial atmosphere is one of the most puzzling enigmas in the planetary sciences. It is suggested here that two sources contributed to its formation, fractionated nebular gases and accreted cometary volatiles. During terrestrial growth, a transient gas envelope was fractionated from nebular composition. This transient atmosphere was mixed with cometary material. The fractionation stage resulted in a high Xe/Kr ratio, with xenon being more isotopically fractionated than krypton. Comets delivered volatiles having low Xe/Kr ratios and solar isotopic compositions. The resulting atmosphere had a near-solar Xe/Kr ratio, almost unfractionated krypton delivered by comets, and fractionated xenon inherited from the fractionation episode. The dual origin therefore provides an elegant solution to the long-standing “missing xenon” paradox. It is demonstrated that such a model could explain the isotopic and elemental abundances of Ne, Ar, Kr, and Xe in the terrestrial atmosphere.     

Noble gas study of the Saratov L4 chondrite

Abstract– We have determined the elemental abundances and the isotopic compositions of noble gases in a bulk sample and an HF/HCl residue of the Saratov (L4) chondrite using stepwise heating. The Ar, Kr, and Xe concentrations in the HF/HCl residue are two orders of magnitude higher than those in the bulk sample, while He and Ne concentrations from both are comparable. The residue contains only a portion of the trapped heavy noble gases in Saratov; 40 ± 9% for ³⁶Ar, 58 ± 12% for ⁸⁴Kr, and 48 ± 10% for ¹³²Xe, respectively. The heavy noble gas elemental pattern in the dissolved fraction is similar to that in the residue but has high release temperatures. Xenon isotopic ratios of the HF/HCl residue indicate that there is no Xe‐HL in Saratov, but Ne isotopic ratios in the HF/HCl residue lie on a straight line connecting the cosmogenic component and a composition between Ne‐Q and Ne‐HL. This implies that the Ne isotopic composition of Q has been changed by incorporating Ne‐HL (Huss et al. 1996) or by being mass fractionated during the thermal metamorphism. However, it is most likely that the Ne‐Q in Saratov is intrinsically different from this component in other meteorites. The evidence of this is a lack of correlation between the isotopic ratio of Ne‐Q and petrologic types of meteorites (Busemann et al. 2000). A neutron capture effect was observed in the Kr isotopes, and this process also affected the ¹²⁸Xe/¹³²Xe ratio. The ³He and ²¹Ne exposure ages for the bulk sample are 33 and 35 Ma, respectively.     

History of lunar meteorites Queen Alexandra Range 93069, Asuka 881757, and Yamato 793169 based on noble gas isotopic abundances,radionuclide concentrations,and chemical composition

Abstract— We investigated the characteristics and history of lunar meteorites Queen Alexandra Range 93069, Yamato 793169 and Asuka 881757 based on the abundances of all stable noble gas isotopes, the concentrations of the radionuclides ¹⁰Be, ²⁶Al, ³⁶Cl, and ⁸¹Kr, and the abundances of Mg, Al, K, Ca, Fe, Cl, Sr, Y, Zr, Ba, and La. Based on the solar wind and cosmic-ray irradiations, QUE 93069 is the most mature lunar meteorite studied up to now. The ⁴⁰Ar/³⁶Ar ratio of the trapped component is 1.87 ± 0.16. This ratio corresponds to a time when the material was exposed to solar and lunar atmospheric volatiles ～400 Ma ago. On the other hand, Yamato 793169 and Asuka 881757 contain very little or no solar noble gases, which indicates that these materials resided in the top layer of the lunar regolith only briefly or not at all. For all lunar meteorites, we observe a positive correlation of the concentrations of cosmic-ray produced with trapped solar noble gases. The duration of lunar regolith residence for the lunar meteorites was calculated based on cosmic-ray produced ²¹Ne, ³⁸Ar, ⁷⁸Kr, ⁸³Kr, and ¹²⁶Xe and appropriate production rates that were derived based on the target element abundances and the shielding indicator ¹³¹Xe/¹²⁶Xe. For QUE 93069, Yamato 793169, and Asuka 881757, we obtained 1000 ± 400 Ma, 50 ± 10 Ma, and <1 Ma, respectively. Both Asuka 881757 and Yamato 793169 show losses of radiogenic ⁴He from U and Th decay and Yamato 793169 also ⁴⁰Ar loss from K-decay. For Asuka 881757, we calculate a K-Ar gas retention age of 3100 ± 600 Ma and a ²⁴⁴Pu-¹³⁶Xe fission age of 4240 ± 170 Ma. This age is one of the oldest formation ages ever observed for a lunar basalt. The exposure history of QUE 93069 after ejection from the Moon was derived from the radionuclide concentrations: ejection 0.16 ± 0.03 Ma ago, duration of Moon-Earth transit 0.15 ± 0.02 Ma and fall on Earth <0.015 Ma ago. This ejection event is distinguished temporally from those which produced the other lunar meteorites. We conclude that six to eight events are necessary to eject all the known lunar meteorites.     

Acid‐susceptive material as a host phase of argon‐rich noble gas in the carbonaceous chondrite Ningqiang

Abstract— A fine‐grained dark inclusion in the Ningqiang carbonaceous chondrite consists of relatively pristine solar nebular materials and has high concentrations of heavy primordial rare gases. Trapped 36Ar concentration amounts to 6 times 10^?6 cc STP/g, which is higher than that of Ningqiang host by a factor of three. Light HF‐HCl etching of the dark inclusion removed 86, 73, and 64% of the primordial ³⁶Ar, ⁸⁴Kr, and ¹³²Xe, respectively. Thus, the majority of the noble gases in this inclusion are located in very acid‐susceptive material. Based on the elemental composition, the noble gases lost from the dark inclusion during the acid‐treatments are Ar‐rich, and the noble gases remaining in the inclusion are Q and HL gases. Transmission electron microscopy showed that the acid treatments removed thin Si, Mg, and Fe‐rich amorphous rims present around small olivine and pyroxene grains in the dark inclusion, suggesting that the Ar‐rich gases reside in the amorphous layers. A possible origin of the Ar‐rich gases is the acquisition of noble‐gas ions with a composition fractionated relative to solar abundance favoring the heavy elements by the effect of incomplete ionization under plasma conditions at 8000 K electron temperature.