The enigma of helium and anomalous xenon

Isotopically anomalous xenon in chondrites is closely associated with low-Z noble gases, but there is no helium (or neon) in the noble gas component with normal xenon. The correlation of elemental and isotopic heterogeneities in meteoritic noble gases places stringent limits on the origin of isotopically anomalous elements in meteorites and on the formation of the solar system.     

Isotopically anomalous neon in meteoritic nanodiamonds: Formation during type II supernova explosions

We hypothesize the formation of neon associated with isotopically anomalous xenon (Xe-HL) in meteoritic nanodiamonds and designated as Ne-X through the mixing of the Ne-HL and Ne-S subcomponents. The Ne-HL subcomponent is neon from the helium (He/C) zone of a type II supernova or a mixture of neon from this zone and its hydrogen zone, while the Ne-S subcomponent is spallation neon formed during a supernova explosion in nuclear spallation reactions induced by high-energy protons. Based on this hypothesis and the presumed abundances of neon isotopes in the zones of a high-mass (25M _⊙) supernova after its explosion, we have calculated the abundances of neon components in nanodiamond separates and its grain-size fractions. Our calculations have shown the following. (1) The main source of Ne-HL is neon from the helium zone of the supernova; as a result, the ²⁰Ne/²²Ne and ²¹Ne/²²Ne ratios for Ne-X are 0.26 ± 0.03 and 0.19 ± 0.04, respectively. The isotopic composition of Ne-X is identical to that for Ne-A2 if Ne-HL is produced by the mixing of neon from the helium and hydrogen zones in proportion 1: 1.06. (2) In meteoritic nanodiamonds, the main neon abundance is determined by neon of the P3 component (Ne-P3). Ne-P3 is retained during thermal metamorphism, because it is sited in traps of the crystal lattice of diamond with a high energy of its activation. (3) The Ne-X/Ne-P3 ratio increases with nanodiamond grain size; as a result, there is no need to invoke an additional neon component (Ne-P6) to interpret the data on neon in meteoritic nanodiamonds.     

A New Martian Meteorite: the Dhofar 019 Shergottite with an Exposure Age of 20 Million Years

The isotopic composition of the noble gases of the new Martian meteorite, the Dhofar 019 shergottite, found in the desert in the territory of the Sultanate of Oman on January 24, 2001, was investigated. Stepwise thermal annealing with isotopic analysis of each of the noble-gas temperature fractions was employed to determine the component composition. The concentration of the trapped noble gases in the new Martian meteorite Dhofar 019 is relatively high, although it lies within the range of concentrations in known SNC meteorites. A characteristic feature of all the trapped noble gases is the presence of two main components: a low-temperature, probably terrestrial atmospheric, component, trapped during the weathering of the meteorite on Earth, and a high-temperature trapped Martian component. Owing to the different ratios of the quantities of the two components, the trapped neon, argon, krypton, and xenon differ markedly in the kinetics of their release. The isotopic composition of the noble gases varies accordingly. The trapped xenon was found to contain two Martian components. One of them, with typical ratios of ¹²⁹Xe/¹³²Xe and ¹³²Xe/⁸⁴Kr, is representative of xenon and krypton of the Martian atmosphere; the other, of gases of the Martian mantle. Variations of the isotopic compositions of helium, neon, and argon (and also, to a lesser extent, of krypton and xenon) during the thermal annealing of the Dhofar 019 meteorite clearly point to a large proportion of cosmogenic as well as trapped components. The concentration of cosmogenic neon and argon in the meteorite is unusually high. This corresponds to a maximum exposure age among other SNC meteorites: 20 million years. Estimates of the potassium–argon age (gas-retention age) yielded the figure of 560 million years, which is within the range of values obtained for SNC meteorites by other authors, who used the rubidium–strontium and the potassium–argon technique.     

Krypton and xenon from the solar wind and solar energetic particles in two lunar ilmenites of different antiquity

Abstract We present Kr and Xe isotope data obtained by closed system stepped etching of ilmenite separates from two lunar samples exposed to the solar corpuscular radiation at different epochs. Helium, neon, and argon in the same samples were reported to consist of two components: isotopically unfractionated solar wind (SW) released in the first steps, and an isotopically heavier component (SEP) released later and, thus, sited at larger depth. The same release characteristic is now observed for the heavy noble gases. We also conclude that solar Kr and Xe consist of two isotopically different components, implanted with different energies. The SW-Kr in a recently irradiated soil has a composition very close to atmospheric Kr, which agrees with other newly reported data from stepped etch- and combustion runs. No clear evidence for temporally variable SW-Kr or SW-Xe spectra was found. “Surface correlated” Kr and Xe components “SUCOR” and “BEOC 12001” are a mixture of SW and SEP. The isotopic fractionation factors relating SW and SEP are close to the square of the mass ratios for all five noble gases. We infer that the measured Kr/Xe ratio in ilmenite is essentially identical to this ratio in the solar corpuscular radiation.     

Noble gases in presolar diamonds I: Three distinct components and their implications for diamond origins

Abstract— High-purity separates of presolar diamond were prepared from 14 primitive chondrites from 7 compositional groups. Their noble gases were measured using stepped pyrolysis. Three distinct noble gas components are present in diamonds, HL, P3, and P6, each of which is found to consist of five noble gases. P3 , released between 200 °C and 900 °C, has a “planetary” elemental abundance pattern and roughly “normal” isotopic ratios. HL , consisting of isotopically anomalous Xe-HL and Kr-H, Ar with high ³⁸Ar/³⁶Ar, and most of the gas making up Ne-A2 and He-A, is released between 1100 °C and 1600 °C. HL has “planetary” elemental ratios, except that it has much more He and Ne than other known “planetary” components. HL gases are carried in the bulk diamonds, not in some trace phase. P6 has a slightly higher median release temperature than HL and is not cleanly separated from HL by stepped pyrolysis. Our data suggest that P6 has roughly “normal” isotopic compositions and “planetary” elemental ratios. Both P3 and P6 seem to be isotopically distinct from P1, the dominant “planetary” noble-gas component in primitive chondrites. Release characteristics suggest that HL and P6 are sited in different carriers within the diamond fractions, while P3 may be sited near the surfaces of the diamonds. We find no evidence of separability of Xe-H and Xe-L or other isotopic variations in the HL component. However, because ～10¹⁰ diamonds are required to measure a Xe composition, a lack of isotopic variability does not constrain diamonds to come from a single source. In fact, the high abundance of diamonds in primitive chondrites and the presence of at least three distinct noble-gas components strongly suggest that diamonds originated in many sources. Relative abundances of noble-gas components in diamonds correlate with degree of thermal processing (see companion paper), indicating that all meteorites sampled essentially the same mixture of diamonds. That mixture was probably inherited from the Sun's parent molecular cloud.     

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 gases in presolar diamonds III: Implications of ion implantation experiments with synthetic nanodiamonds

Abstract— A series of experiments carried out by Koscheev et al. (1998, 2001, 2004, 2005) showed that the bimodal release of heavy noble gases from meteoritic nanodiamonds can be reproduced by a single implanted component. This paper investigates the implications of this result for interpreting the noble gas compositions of meteoritic nanodiamonds and for their origin and history. If the bimodal release exhibited by meteorite diamonds reflects release of the P3 noble gas component, then the composition inferred for the pure Xe‐HL end member changes slightly, the excesses of heavy krypton isotopes that define Kr‐H become less extreme, evidence appears for a Kr‐L component, and the nucleosynthetic contribution to argon becomes much smaller. After correction for cosmogenic neon inherited from the host meteorites, the neon in presolar diamonds shows evidence for pre‐irradiation, perhaps in interstellar space, and a nucleosynthetic component perhaps consistent with a supernova source. After a similar correction, helium also shows evidence for presolar irradiation and/or a nucleosynthetic component. For the case of presolar irradiation, due to the small size of the diamonds, a large entity must have been irradiated and recoiling product nuclei collected by the nanodiamonds. The high ³He/²¹Ne ratio (?43) calls for a target with a (C + O)/heavier‐element ratio higher than in chondritic abundances. Bulk gas + dust (cosmic abundances) meet this criteria, as would solids enriched in carbonaceous material. The long recoil range of cosmogenic ³He argues against a specific phase. The excess ³He in presolar diamonds may represent trapped cosmic rays rather than cosmogenic ³He produced in the vicinity of the diamond crystals.     

Helium and neon in comet 81P/Wild 2 samples from the NASA Stardust mission

Helium and neon distributions are reported for a variety of Stardust comet 81P/Wild 2 samples, including particle tracks and terminal particles, cell surface and subsurface slices from the comet coma and interstellar particle collection trays, and numerous small aerogel blocks extracted from comet cells C2044 and C2086. Discussions and conclusions in several abstracts published during the course of the investigation are included, along with the relevant data. Measured isotope ratios span a broad range, implying a similar range for noble gas carriers in the Wild 2 coma. The meteoritic phase Q‐²⁰Ne/²²Ne ratio was observed in several samples. Some of these, and others, exhibit ²¹Ne excesses too large for attribution to spallation by galactic cosmic ray irradiation, suggesting exposure to a solar proton flux greatly enhanced above current levels in an early near‐Sun environment. Still others display evidence for a solar wind component, particularly one C2086 block with large abundances of isotopically solar‐like helium and neon. Eighty‐nine small aerogel samples were cut from depths up to several millimeters below the cell C2044 surface and several millimeters away from the axis of major track T41. A fraction of these yielded measurable and variable helium and neon abundances and isotope ratios, although none contained visible tracks or carrier particle fragments and their locations were beyond estimated penetration ranges for small particles or ions incident on the cell surface, or for lateral ejecta from T41. Finding plausible emplacement mechanisms and sources for these gases is a significant challenge raised by this study.     

Charge States of Krypton and Xenon in the Solar Wind

We calculate charge state distributions of Kr and Xe in a model for two different types of solar wind using the effective ionization and recombination rates provided from the OPEN_ADAS data base. The charge states of heavy elements in the solar wind are essential for estimating the efficiency of Coulomb drag in the inner corona. We find that xenon ions experience particularly low Coulomb drag from protons in the inner corona, comparable to the notoriously weak drag of protons on helium ions. It has been found long ago that helium in the solar wind can be strongly depleted near interplanetary current sheets, whereas coronal mass ejecta are sometimes strongly enriched in helium. We argue that if the extraordinary variability of the helium abundance in the solar wind is due to inefficient Coulomb drag, the xenon abundance must vary strongly. In fact, a secular decrease of the solar wind xenon abundance relative to the other heavier noble gases (Ne, Ar, Kr) has been postulated based on a comparison of noble gases in recently irradiated and ancient samples of ilmenite in the lunar regolith. We conclude that decreasing solar activity and decreasing frequency of coronal mass ejections over the solar lifetime might be responsible for a secularly decreasing abundance of xenon in the solar wind.     

银河系化学元素的丰度特征和合成图像(Ⅱ):太阳系原始同位素丰度异常及其解释

太阳系原始同位素组成是研究太阳系起源和演化的基础。评述了太阳星云的原始放射性核素丰度特征及解释此丰度特征的分子云自增丰模型、AGB星污染模型和散裂反应模型。陨石包体中前太阳矿物颗粒的同位素组成异常表明,前太阳颗粒中低密度石墨、X型碳硅石可能来源于超新星爆发,而AGB星或红巨星被认为是尖晶石和碳硅石的最可能的恒星来源。太阳系中比较特殊的氖和氙的同位素组成异常也与超新星爆发密切相关。     

The lunar atmosphere

In contrast to earth, the atmosphere of the moon is exceedingly tenuous and appears to consist mainly of noble gases. The solar wind impinges on the lunar surface, supplying detectable amounts of helium, neon and ³⁶Ar. Influxes of solar wind protons and carbon and nitrogen ions are significant, but atmospheric gases containing these elements have not been positively identified. Radiogenic ⁴⁰Ar and ²²²Rn produced within the moon have been detected. The present rate of effusion of argon from the moon accounts for about 0.4% of the total production of ⁴⁰Ar due to decay of ⁴⁰K if the average abundance of potassium in the moon is 1000 ppm. Lack of weathering processes in the regolith suggests that most of the atmospheric ⁴⁰Ar originates deep in the lunar interior, perhaps in a partially molten core. If so, other gases may be vented along with the argon.     

Volatile transport on inhomogeneous surfaces: I – Analytic expressions,with application to Pluto’s day

The two orders of magnitude drop between the measured atmospheric abundances of non-radiogenic argon, krypton and xenon in Earth versus Mars is striking. Here, in order to account for this difference, we explore the hypothesis that clathrate deposits incorporated into the current martian cryosphere have sequestered significant amounts of these noble gases assuming they were initially present in the paleoatmosphere in quantities similar to those measured on Earth (in mass of noble gas per unit mass of the planet). To do so, we use a statistical-thermodynamic model that predicts the clathrate composition formed from a carbon dioxide-dominated paleoatmosphere whose surface pressure ranges up to 3 bars. The influence of the presence of atmospheric sulfur dioxide on clathrate composition is investigated and we find that it does not alter the trapping efficiencies of other minor species. Assuming nominal structural parameters for the clathrate cages, we find that a carbon dioxide equivalent pressure of 0.03 and 0.9 bar is sufficient to trap masses of xenon and krypton, respectively, equivalent to those found on Earth in the clathrate deposits of the cryosphere. In this case, the amount of trapped argon is not sufficient to explain the measured Earth/Mars argon abundance ratio in the considered pressure range. In contrast, with a 2% contraction of the clathrate cages, masses of xenon, krypton and argon at least equivalent to those found on Earth can be incorporated into clathrates if one assumes the trapping of carbon dioxide at equivalent atmospheric pressures of ～2.3 bar. The proposed clathrate trapping mechanism could have then played an important role in the shaping of the current martian atmosphere.     

Collisional broadening and shift of the alkali resonance lines

We use the 6-8-12 interatomic potential, with a suitable scaling for the relevant atomic radii, to reproduce the measured broadening and shift of the alkali resonance lines perturbed by noble gases, at temperatures of 500 K.Then, using the fit to the data with helium and neon as perturbers, we compute new values for the broadening and shift of the alkali resonance lines due to atomic hydrogen, at the temperature of 5000 K, which are of interest in the analysis of solar and stellar spectra, and discuss the reliability of these results.     

Neon,argon, and chlorine abundance gradients from type II planetary nebulae

Heavy-element abundance gradients derived from type II planetary nebulae (PN) are studied for the elements neon, argon, and chlorine. As in the case of helium, oxygen, sulphur, and probably carbon and nitrogen, the abundance of these elements relative to hydrogen present measurable radial gradients across the galactic disk.     

Noble gases and meteorites

Abstract— Noble gases repeatedly have served to widen the scope of meteorite research. During the first half century of such measurements, the emphasis was on the determination of U, Th/He-gas retention ages of iron meteorites, which is the most unsuitable class of meteorites for such studies. With the realization that the He in these meteorites results from the interaction of cosmic rays with meteoritic matter, meteorites became to be used as “the poor man's space probe” that yielded information on the constancy in time and space of the cosmic radiation. Another widening of scope came with the discovery of extremely high noble gas contents in the outermost layers of the individual grains that make up stony meteorites. These gases are of solar origin; they have been implanted as low-energy solar wind (SW) or as solar energetic particles (SEP) into the grains before their compaction. Presently they offer the only opportunity to precisely measure the isotopic composition of solar matter and to learn about potential changes of the Sun in time. Stony meteorites of the “carbonaceous” variety contain “stardust” that carries the undiluted nucleosynthesis products of individual stars that yield incredibly detailed information concerning the parameters that prevailed during the synthesis.     

Interstellar graphite in meteorites: Isotopic compositions and structural properties of single graphite grains from Murchison

Abstract— One hundred forty-three carbon grains, ranging in size from 2 to 8 μm, from two chemical and physical separates from the Murchison CM2 chondrite, were analyzed by ion microprobe mass spectrometry for their C- and N-isotopic compositions. Both separates are enriched in the exotic noble gas component Ne-E(L). Ninety grains were also analyzed for their H and O contents and 118, for Si. Thirteen grains were analyzed by micro-sampling laser Raman spectroscopy. Round grains have large C-isotopic anomalies with ¹²C/¹³C ratios ranging from 7 to 4500 (terrestrial ratio = 89). Nitrogen in these grains is also anomalous but shows much smaller deviations from the terrestrial composition, ¹⁴N/¹⁵N ratios ranging from 193 to 680 (terrestrial ratio = 272). Spherulitic aggregates and non-round compact grains have normal C-isotopic ratios but ¹⁵N excesses (up to 35%). Raman spectra of the analyzed grains indicate varying degrees of crystalline disorder of graphite with estimated in-plane crystallite dimensions varying from 18 Å (highly disordered, similar to terrestrial kerogen) to ～750 Å (well-crystallized graphite). Element contents of H, O, and Si are correlated with one another, and H and O are probably present in the form of organic molecules. On the basis of morphology, the round grains fall into two groups: grains with smooth, shell-like surfaces (“onions”) and grains that appear to be dense aggregates of small scales (“cauliflowers”). “Onions” tend to have lower trace element contents, isotopically light C (¹²C/¹³C > 89) and a high degree of crystalline order, whereas “cauliflowers” have a larger spread in trace element contents and C-isotopic ratios (they range from isotopically light to heavy) but tend to have a low degree of crystalline order. However, these differences exist only on average, and no clear distinction can be made for individual grains. A few limited conclusions can be drawn about the astrophysical origin of the carbon grains of this study. The ¹⁵N excesses in spherulitic aggregates and non-round grains can be explained as the result of ion-molecule reactions in molecular clouds. The round grains, on the other hand, must have formed in stellar atmospheres (circumstellar grains). Grains with isotopically light C must have formed in stellar environments characterized by He-burning, either in the atmosphere of Wolf-Rayet stars during the WC phase or in the He-burning, ¹²C-rich zone of a massive star, ejected by a supernova explosion. Isotopically heavy C is produced by H-burning in the CNO cycle. Possible sources for grains with heavy C are carbon stars (AGB stars during the thermally pulsing phase) or novae, but the detailed distribution of ¹²C/¹³C ratios agree neither with the distribution observed in carbon stars nor with theoretical predictions for these two types of stellar sources.     

On the problem of Solar System origin: The regularities of noble gas fractionation in shock waves

The effects of the last supernova explosion before the formation of the Solar System are considered using noble gases as examples. Acceleration of generated supernova matter in the explosive shock wave led to its initial fractionation and to the formation of small-scale isotopic heterogeneity of primordial matter. This is fixed as some isotopic anomalies in high-temperature phases of the earliest condensates of carbonaceous chondrites, as well as in the isotopic systems of noble gases, and is the basis of the supernova phenomenon. Two main manifestations of shock-wave acceleration in noble gases are investigated: the change in the isotopic ratios of their cosmogenic components due to the increasing hardness of the spectrum of nuclear-active particles and the fractionation of gases, namely, the enrichment of their isotopic systems with heavier isotopes. The reality of the processes under consideration is demonstrated through the example of noble gases of solar corpuscular radiation in lunar ilmenites. The absence of r-process products among extinct radionuclides in Ca-and Al-rich inclusions (CAI) of carbonaceous chondrites with a formation interval of less than or equal to 1 Ma supports the idea that the last supernova was an Ia-type supernova, which possibly played an important role in the origin of the Solar System.     

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.     

Neutrino detection with CLEAN

This article describes CLEAN, an approach to the detection of low-energy solar neutrinos and neutrinos released from supernovae. The CLEAN concept is based on the detection of elastic scattering events (neutrino–electron scattering and neutrino–nuclear scattering) in liquified noble gases such as liquid helium, liquid neon, and liquid xenon, all of which scintillate brightly in the ultraviolet. Key to the CLEAN technique is the use of a thin film of wavelength-shifting fluor to convert the ultraviolet scintillation light to the visible, thereby allowing detection by conventional photomultipliers.

Liquid neon is a particularly promising medium for CLEAN. Because liquid neon has a high scintillation yield, has no long-lived radioactive isotopes, and can be easily purified by use of cold traps, it is an ideal medium for the detection of rare nuclear events. In addition, neon is inexpensive, dense, and transparent to its own scintillation light, making it practical for use in a large self-shielding apparatus. The central region of a full-sized detector would be a stainless steel tank holding approximately 135 metric tons of liquid neon. Inside the tank and suspended in the liquid neon would be several thousand photomultipliers.

Monte Carlo simulations of gamma ray backgrounds have been performed assuming liquid neon as both shielding and detection medium. Gamma ray events occur with high probability in the outer parts of the detector. In contrast, neutrino scattering events occur uniformly throughout the detector. We discriminate background gamma ray events from events of interest based on a spatial maximum likelihood method estimate of event location. Background estimates for CLEAN are presented, as well as an evaluation of the sensitivity of the detector for p–p neutrinos. Given these simulations, the physics potential of the CLEAN approach is evaluated.     

Microscopic search for the carrier phase Q of the trapped planetary noble gases in Allende,Leoville and Vigarano

Abstract— High‐resolution transmission electron microscopy micrographs of acid‐resistant residues of the Allende, Leoville, and Vigarano meteorites show a great variety of carbon structures: curved and frequently twisted and intertwined graphene sheets, abundant carbon black‐like particles, and hollow “sacs”. It is suggested that perhaps all of these are carriers for the planetary Q‐noble gases in these meteorites. Most of these materials are pyrocarbons that probably formed by the pyrolysis of hydrocarbons either in a gas phase, or on hot surfaces of minerals. An attempt was made to analyze for argon with particle‐induced x‐ray emission in 143 spots of grains of floating and suspended matter from freeze‐dry cycles of an Allende bulk sample in water, and floating “black balls” from sonication in water of samples from the Allende meteorite. The chemical compositions of these particles were obtained, but x‐ray signals at the wavelength of argon were obtained on only a few spots.