Noble gases in Muong Nong‐type tektites and their implications

Abstract— We have the elemental abundances and isotopic compositions of noble gases in Muong Nong‐type tektites from the Australasian strewn field by crushing and by total fusion of the samples. We found that the abundances of the heavy noble gases are significantly enriched in Muong Nong‐type tektites compared to those in normal splash‐form tektites from the same strewn field. Neon enrichments were also observed in the Muong Nong‐type tektites, but the Ne/Ar ratios were lower than those in splash‐form tektites because of the higher Ar contents in the former. The absolute concentrations of the heavy noble gases in Muong Nong‐type tektites are similar to those in impact glasses. The isotopic ratios of the noble gases in Muong Nong‐type tektites are mostly identical to those in air, except for the presence of radiogenic ⁴⁰Ar. The obtained K‐Ar ages for Muong Nong‐type tektites were about 0.7 Myr, similar to ages of other Australasian tektites. The crushing experiments suggest that the noble gases in the Muong Nong‐type tektites reside mostly in vesicles, although Xe was largely affected by adsorbed atmosphere after crushing. We used the partial pressure of the heavy noble gases in vesicles to estimate the barometric pressure in the vesicles of the Muong Nong‐type tektites. Likely, Muong Nong‐type tektites solidified at the altitude (between the surface and a maximum height of 8–30 km) lower than that for splash‐form tektites.     

Mechanism of Muong Nong-type tektite formation and speculation on the source of Australasian tektites

Abstract The source crater of the youngest and largest of the tektite strewnfields, the Australasian strewnfield, has not been located. A number of lines of evidence indicate that the Muong Nong-type tektites, primarily found in Indochina, are more primitive than the much more abundant and widespread splash-form tektites, and are proximal to the source. In this study the spatial distribution of Muong Nong-type tektite sites and chemical character have been used to indicate the approximate location of the source. The variation of Muong Nong-type tektite chemical composition appears to be caused by mixing of two silicate rock end-members and a small amount of limestone, and not by vapor fractionation. The variation in composition is not random, and does not support in-situ melting or multiple impact theories. The distribution of both Muong Nong and splash-form tektite sites suggest the source is in a limited area near the southern part of the Thailand-Laos border.     

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.     

Trace element study of high- and low-refractive index Muong Nong-type tektites from Indochina

Abstract— Previous work indicates that Muong Nong-type tektites from Indochina with low refractive indices and high silica contents contain relict mineral grains while those with high refractive indices and low silica contents do not. Instrumental Neutron Activation Analysis (INAA) was used to determine selected trace element concentrations for four Muong Nong-type tektites with high refractive indices and no relict mineral inclusions and one with low refractive index and relict inclusions, to determine if there are any systematic differences in trace element compositions between the two groups. The data also were compared with published trace element data for sixteen Muong Nong-type tektites which have low refractive indices and, therefore, should contain relict inclusions. Except for Ta which had lower concentrations in the high refractive index group, there is no consistent difference in trace element compositions between the two groups. We interpret these results to indicate a single, slightly heterogeneous source for the Muong Nong-type tektites, rather than different source regions.     

Noble gases and nitrogen in Raghunathpura (IIAB) and Nyaung (IIIAB) iron meteorites

Noble gases and nitrogen were measured in two adjacent samples each from the Raghunathpura (IIAB) and the Nyaung (IIIAB) iron meteorite falls. Light noble gases in both the meteorites were of pure cosmogenic origin. Using (³He/⁴He)_c ratios and the production systematic of Ammon et al. ( 2009 ), we estimated the sample depth and meteoroid size for Nyaung (~8 cm depth in a ~15 cm radius object) and Raghunathpura (~12–14 cm depth in a ~25 cm object). We derived cosmic ray exposure ages of 1710 ± 256 Ma (for Nyaung, the highest reported so far for the IIIAB group) and 224 ± 34 Ma (for Raghunathpura). Variable amounts of trapped Kr and Xe were found in both meteorites. The phase Q‐like elemental ratio (⁸⁴Kr/¹³²Xe) suggests that the trapped component is of indigenous origin, and most likely hosted in the heterogeneously distributed micro‐inclusions of troilite/schreibersite. Trapped phase Q component is being reported for the first time, for a IIAB iron meteorite. Both meteorites showed light isotopic composition for nitrogen, and need at least two N components to explain the observed N isotopic systematic. Variable amounts of trapped noble gases and the presence of more than one N component suggest that the magmatic process that formed the parent body of these meteorites either could not completely homogenize or completely degas all the phases.     

Noble gases in ureilites released by crushing

Abstract— Noble gases in two ureilites, Kenna and Allan Hills (ALH) 78019, were measured with two extraction methods: mechanical crushing in a vacuum and heating. Large amounts of noble gases were released by crushing, up to 26.5% of ¹³²Xe from ALH 78019 relative to the bulk concentration. Isotopic ratios of the crush‐released Ne of ALH 78019 resemble those of the trapped Ne components determined for some ureilites or terrestrial atmosphere, while the crush‐released He and Ne from Kenna are mostly cosmogenic. The crush‐released Xe of ALH 78019 and Kenna is similar in isotopic composition to Q gas, which indicates that the crush‐released noble gases are indigenous and not caused by contamination from terrestrial atmosphere. In contrast to the similarities in isotopic composition with the bulk samples, light elements in the crush‐released noble gases are depleted relative to Xe and distinct from those of each bulk sample. This depletion is prominent especially in the ²⁰Ne/¹³²Xe ratio of ALH 78019 and the ³⁶Ar/¹³²Xe ratio of Kenna. The values of measured ³He/²¹Ne for the gases released by crushing are significantly higher than those for heating‐released gases. This suggests that host phases of the crush‐released gases might be carbonaceous because cosmogenic Ne is produced mainly from elements with a mass number larger than Ne. Based on our optical microscopic observation, tabular‐foliated graphite is the major carbon mineral in ALH 78019, while Kenna contains abundant polycrystalline graphite aggregates and diamonds along with minor foliated graphite. There are many inclusions at the edge and within the interior of olivine grains that are reduced by carbonaceous material. Gaps can be seen at the boundary between carbonaceous material and silicates. Considering these petrologic and noble gas features, we infer that possible host phases of crush‐released noble gases are graphite, inclusions in reduction rims, and gaps between carbonaceous materials and silicates. The elemental ratios of noble gases released by crushing can be explained by fractionation, assuming that the starting noble gas composition is the same as that of amorphous carbon in ALH 78019. The crush‐released noble gases are the minor part of trapped noble gases in ureilites but could be an important clue to the thermal history of the ureilite parent body. Further investigation is needed to identify the host phases of the crush‐released noble gases.     

Noble gases and strontium isotopes in the unique meteorite Divnoe

Abstract— We present an isotope study of noble gases in Divnoe, an anomalous meteorite, and also Rb-Sr and K-Ar dating of this meteorite. The relatively young Rb-Sr age obtained (3.39 Ga) seems doubtful and, most probably, results from weathering or contamination. The ancient K-Ar age (4.67^+0.20_–0.40), together with clear excess of ¹²⁹Xe, allows the suggestion of very early formation of the Divnoe meteorite. Concentrations and isotope ratios of noble gases in Divnoe are: 17.9 ≤ ³He ≤ 29.0 × 10^?8; ²⁰Ne = 6.22 × 10^?8; 2.44 ≤ ³⁶Ar ≤ 5.10 × 10^?8; ¹³⁰Xe = 41.3 × 10^?12 cm³/g; 0.079 ≤ ³He/⁴He ≤ 0.193; ²⁰Ne/²²Ne = 0.860; ²¹Ne/²²Ne = 0.927; 3.47 ≤ ⁴⁰Ar/³⁶Ar ≤ 9.47; 2.22 ≤ 36Ar/³⁸Ar ≤ 3.27; ¹²⁹Xe/¹³²Xe = 1.09. The exposure age calculated from cosmogenic ³He, ²¹Ne, and ³⁸Ar is 17.9 ± 0.9 Ma. On the basis of the isotope data for the noble gases and O, and abundances of K, Rb, and Sr, an attempt was made to estimate the relationship of Divnoe to other meteorite types. The O-isotope characteristics of Divnoe are clearly distinct from those of ordinary chondrites, acapulcoites/lodranites, and SNC meteorites (Petaev et al., 1994, Clayton, 1993). In plots of ¹³⁶Xe vs. ¹²⁹Xe/¹³⁰Xe, the Divnoe data fall outside of the data fields for carbonaceous and enstatite chondrites. The light noble gas data, especially the ⁴⁰Ar/³⁸Ar ratio, and the ⁴⁰Ar, ³⁸Ar, ³He, and ⁴He contents of Divnoe differ significantly from those of all meteorite types except diogenites. The K, Rb, and Sr abundances in Divnoe are substantially lower than in most other meteorites. In the concentrations of these elements, as well as in the REE pattern, the Divnoe meteorite is similar only to diogenites. Divnoe probably should be treated as a restite remaining after partial melting of the chondritic mantle of a parent asteroid body.     

Noble gases in enstatite chondrites released by stepped crushing and heating

Abstract– Enstatite chondrites (ECs) were subjected to noble gas analyses using stepped crushing and pyrolysis extraction methods. ECs can be classified into subsolar gas‐carrying and subsolar gas‐free ECs based on the ³⁶Ar/⁸⁴Kr/¹³²Xe ratios. For subsolar gas‐free ECs, elemental ratios, and Xe isotopic compositions indicate that Q gas is the dominant trapped component, the Q gas concentration can be correlated with the petrologic type, reasonably explained by gas release from a common EC parental material during subsequent heating. Atmospheric Xe with sub‐Q elemental ratios is found in Antarctic E3s at 600–800 °C and through crushing. The ¹³²Xe released in these fractions accounts for 30–60% of the bulk concentrations. Hence, the sub‐Q signature is generally due to contamination of elementally fractionated atmosphere. Subsolar gas is mainly released (up to 78% of the bulk ³⁶Ar) at 1300–1600 °C and through crushing, suggesting that enstatite and friable phases are the host phases. Subsolar gas is isotopically identical to solar gas, but elementally fractionated. These observations are consistent with a previous study, which suggested that subsolar gas could be fractionated solar wind having been implanted into chondrule precursors ( Okazaki et al. 2001 ). Unlike subsolar gas‐free ECs, the primordial gas concentrations of subsolar gas‐carrying ECs are not simply correlated with the petrologic type. It is inferred that subsolar gas‐rich chondrules were heterogeneously distributed in the solar nebula and accreted to form subsolar gas‐carrying ECs. Subsequent metamorphic and impact‐shock heating events have affected noble gas compositions to various degrees.     

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.     

Distribution of noble gases in Chinese tektites: Implication for neon solubility in natural glasses

Abstract— Five indochinites from Hainan Island and the Leizhou Peninsula, China were analyzed for noble gas abundances and isotopic ratios. These splash‐form tektites show vesiculation ranging from 0.4 vol% to 8 vol%, as determined by digital image analysis (software SXM®) on thin section photographs. To study the distribution of noble gases in vesicles and in glass, the gases were extracted by heating and by crushing, respectively, on 2 aliquots of the same sample. The results show that 5 to 53% of the total measured ²⁰Ne resides in vesicles. The calculated concentration of neon dissolved in the glass is higher (0.7‐1 times 10^?7 cm³STP/g) than that expected from solubility equilibrium (1 times 10^?8 cm³STP/g), assuming solubility data from MORB glasses. The neon concentration of splash‐form tektites, those analyzed in this work and those from other strewn‐fields worldwide, is correlated with the SiO₂ content of glass and with the nonbridging oxygen per tetrahedral cation in the melt (hereafter NBO/T ratio), the latter being an index of the free‐volume in the silica network where neon could be dissolved. These correlations suggest that the glass structure of tektite has a larger free‐volume available for dissolving noble gases than MORB glasses.     

Noble gases in twenty-one Saharan LL-chondrites: Exposure ages and possible pairings

Abstract— Nineteen LL-chondrites and two L/LL-chondrites (Adrar 003 and Tanezrouft 010) from the Saharan desert of Algeria and Libya have been analysed for their He, Ne and Ar composition as well as for their abundance of ⁸⁴Kr and ¹³²Xe. Calculated ²¹Ne cosmic-ray exposure ages vary between 2 and 35 Ma. The age distribution is consistent with that of modern LL-chondrite falls except that no dominant peaks can be observed, especially not the one related to a 15 Ma collisional event. However, the lack of young exposure ages of <8 Ma is obvious. This is a characteristic feature of LL-chondrites. Only one of the 21 LL-chondrites, namely Acfer 066, contains solar gases and is thus considered a regolith breccia. Three specimens reveal considerable loss of ³He, probably due to periods of elevated temperatures in orbits with small perihelion distances. Furthermore, severe loss of ⁴He and ⁴⁰Ar is found in two samples. Considering possible pairings, we suggest 14 individual falls basically on the basis of the noble gas data, the petrographic sub-classification and by taking the find location into consideration. However, there are constraints on confirming pairings solely on the basis of our studies. Thus, we can only exclude individual samples with a unique noble gas fingerprint from paired specimens.     

Noble gases in individual chondrules of the Allende CV3 chondrite

We analyzed noble gases in nine individual chondrules, an assemblage of small chondrules, and four whole‐rock samples of the Allende CV3 chondrite. Major elements were also determined for five chondrules. The cosmic ray exposure ages are calculated from cosmogenic ³He to be 5.17 ± 0.38 and 5.15 ± 0.25 Myr for the averages of the chondrules and whole rocks, respectively, showing no significant pre‐exposure evidence for the studied chondrules. Large amounts of ³⁶Ar, ^80,82Kr, and ¹²⁸Xe produced by neutron capture are observed in most samples; the abundances of these nuclides are correlated among the samples. The epithermal neutron flux and neutron slowing down density are calculated based on [⁸⁰Kr]_n, from which a sample depth of about 30 cm can be calculated. The measured chondrules contain variable amounts of radiogenic ¹²⁹Xe. The abundance ratios of radiogenic ¹²⁹Xe to neutron capture–produced ¹²⁸Xe are rather constant among the studied chondrules; four chondrules give more precise ratios at the high‐temperature fractions, ranging from 1920 ± 80 to 2280 ± 140, which corresponds to a time difference of 3.9 ± 2.4 Myr. It is noticeable that most chondrules also contain ²⁴⁴Pu‐derived fission Xe. The average ²⁴⁴Pu/²³⁸U ratio for nine chondrules is 0.0069 ± 0.0018, which agrees well with the preferred ratio reported for chondrites.     

Noble gases in presolar diamonds II: Component abundances reflect thermal processing

Abstract— Using the isotopic compositions derived in Huss and Lewis, 1994a (Paper I), abundances of the P3, HL, and P6 noble-gas components were determined for 15 diamond separates from primitive chondrites of 8 chondrite classes. Within a meteorite class, the relative abundances of these components correlate with the petrologic subtype of the host meteorite, indicating that metamorphism is primarily responsible for the variations. Relative abundances of P3, HL, and P6 among diamond samples can be understood in terms of thermal processing of a single mixture of diamonds like those now found in CI and CM2 chondrites. With relatively gentle heating, primitive diamonds first lose their low-temperature P3 gases and a “labile” fraction of the HL component. Mass loss associated with release of these components produces an increase in the HL and P6 content of the remaining diamond relative to unprocessed diamond. Higher temperatures initiate destruction of the main HL carrier, while the HL content of the surviving diamonds remains essentially constant. At the same time, the P6 carrier begins to preferentially lose light noble gases. Meteorites that have experienced metamorphic temperatures ?650 °C have lost essentially all of their presolar diamond through chemical reactions with surrounding minerals. The P3 abundance seems to be a function only of the maximum temperature experienced by the diamonds and thus is independent of the nature of the surrounding environment. If all classes inherited the same mixture of primitive diamonds, then P3 abundances would tie together the metamorphic scales in different meteorite classes. However, if the P3 abundance indicates a higher temperature than do other thermometers applicable to the host meteorite, then the P3 abundance may contain information about heating prior to accretion. Diamonds in the least metamorphosed EH, CV, and CO chondrites seem to carry a record of pre-accretionary thermal processing.     

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.     

Halogens in tektites and impact glasses

Abstract— Impact glasses, tektites and some related basement rocks were analyzed for F, Cl, Br and I. The tektite and impact glasses show similar abundance patterns within the groups. Muong Nong-type tektites indicate that the halogens have been depleted in the order I > Br > Cl > F in their melt under oxidizing conditions. For Darwin Glass selective volatilization of F from the melt is a major depleting process. Cl, Br and I are lost to a lesser extent.     

Noble gases in enstatite chondrites I: Exposure ages,pairing, and weathering effects

Abstract— Cosmic‐ray exposure ages calculated from cosmogenic noble gas nuclides are reported for 57 enstatite (E) chondrites, 43 of them were measured for the first time. With a total of 62 individual E chondrites (literature and this data, corrected for pairing) the observed spectrum of ages ranges between 0.07 and 66 Ma. Three clusters seem to develop at about 3.5, 8, and 25 Ma, respectively. Since the uncertainty of ages is estimated to be ～20% (in contrast to 10 to 15% for ordinary chondrites) and the number of examined samples is still comparatively small, these peaks have to be confirmed by more measurements. Regarding the two subgroups, EH and EL chondrites, no systematic trend is apparent in the distribution of cosmic‐ray exposure ages. Several E chondrites yield significantly lower ³⁸Ar ages compared to those calculated from cosmogenic ³He and ²¹Ne. For these E chondrites, we suggest a reduction of cosmogenic ³⁸Ar as a result of weathering. In order to prove the possible influence of terrestrial alteration on the cosmogenic noble gas record of E‐chondritic material, we simulated terrestrial weathering in an experiment of 12 weeks duration. The treatment showed that a significant amount of cosmogenic ³⁸Ar is lost on Earth by the influence of water.     

Noble gases in the Martian meteorite Northwest Africa 2737: A new chassignite signature

Abstract— We report noble gas data for the second chassignite, Northwest Africa (NWA) 2737, which was recently found in the Moroccan desert. The cosmic ray exposure (CRE) age based on cosmogenic ³He, ²¹Ne, and ³⁸Ar around 10–11 Ma is comparable to the CRE ages of Chassigny and the nakhlites and indicates ejection of meteorites belonging to these two families during a discrete event, or a suite of discrete events having occurred in a restricted interval of time. In contrast, U‐Th/He and K/Ar ages <0.5 Ga are in the range of radiometric ages of shergottites, despite a Sm‐Nd signature comparable to that of Chassigny and the nakhlites (Misawa et al. 2005). Overall, the noble gas signature of NWA 2737 resembles that of shergottites rather than that of Chassigny and the nakhlites: NWA 2737 does not contain, in detectable amount, the solar‐like xenon found in Chassigny and thought to characterize the Martian mantle nor apparently fission xenon from ²⁴⁴Pu, which is abundant in Chassigny and some of the nakhlites. In contrast, NWA 2737 contains Martian atmospheric noble gases trapped in amounts comparable to those found in shergottite impact glasses. The loss of Martian mantle noble gases, together with the trapping of Martian atmospheric gases, could have occurred during assimilation of Martian surface components, or more likely during shock metamorphism, which is recorded in the petrology of this meteorite.     

Fluorescence efficiencies of electrons in molecular nitrogen and oxygen gases

Fluorescence efficiencies of electrons in a large number of bands of the N₂ First Positive and O₂⁺ First Negative groups lying in the 4900–10,500 Å wavelength range have been investigated theoretically. The variation of transition moment with internuclear distance is taken into consideration. For the First Positive group of N₂ the calculations are carried out at very low pressure as well as at 600 Torr. In general the present values are higher than the experimental values but in most of the cases fair agreement has been obtained. For the O₂⁺ First Negative group no direct experimental data is available. However, the present ratio of the total efficiency in the O₂⁺ First Negative group to the N₂⁺ First Negative group is found to be in good agreement with the experimental intensity ratio.     

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.     

Noble gases in mineral separates from three shergottites: Shergotty,Zagami, and EETA79001

Abstract— This study provides a complete data set of all five noble gases for bulk samples and mineral separates from three Martian shergottites: Shergotty (bulk, pyroxene, maskelynite), Zagami (bulk, pyroxene, maskelynite), and Elephant Moraine (EET) A79001, lithology A (bulk, pyroxene). We also give a compilation of all noble gas and nitrogen studies performed on these meteorites. Our mean values for cosmic‐ray exposure ages from ³He, ²¹Ne, and ³⁸Ar are 2.48 Myr for Shergotty, 2.73 Myr for Zagami, and 0.65 Myr for EETA79001 lith. A. Serious loss of radiogenic ⁴He due to shock is observed. Cosmogenic neon results for bulk samples from 13 Martian meteorites (new data and literature data) are used in addition to the mineral separates of this study in a new approach to explore evidence of solar cosmic‐ray effects. While a contribution of this low‐energy irradiation is strongly indicated for all of the shergottites, spallation Ne in Chassigny, Allan Hills (ALH) 84001, and the nakhlites is fully explained by galactic cosmic‐ray spallation. Implanted Martian atmospheric gases are present in all mineral separates and the thermal release indicates a near‐surface siting. We derive an estimate for the ⁴⁰Ar/³⁶Ar ratio of the Martian interior component by subtracting from measured Ar in the (K‐poor) pyroxenes the (small) radiogenic component as well as the implanted atmospheric component as indicated from ¹²⁹Xe, * excesses. Unless compromised by the presence of additional components, a high ratio of ～2000 is indicated for Martian interior argon, similar to that in the Martian atmosphere. Since much lower ratios have been inferred for Chassigny and ALH 84001, the result may indicate spatial and/or temporal variations of ⁴⁰Ar/³⁶Ar in the Martian mantle.