Noble gas isotopes and mineral assemblages of Antarctic micrometeorites collected at the meteorite ice field around the Yamato Mountains

Abstract— From November 1998 to January 1999, the 39th Japanese Antarctic Research Expedition (JARE) conducted a large‐scale micrometeorite collection at 3 areas in the meteorite ice field around the Yamato Mountains, Antarctica. The Antarctic micrometeorites (AMMs) collected were ancient cosmic dust particles. This is in contrast with the Dome Fuji AMMs, which were collected previously from fresh snows in 1996 and 1997 and which represent modern micrometeorites. To determine the noble gas concentrations and isotopic compositions of individual AMMs, noble gas analyses were carried out using laser‐gas extraction for 35 unmelted Yamato Mountains AMMs and 3 cosmic spherules. X‐ray diffraction analyses were performed on 13 AMMs before the noble gas measurement and mineral compositions were determined. AMMs are classified into 4 main mineralogical groups, defined from the heating they suffered during atmospheric entry. Heating temperatures of AMMs, inferred from their mineral compositions, are correlated with ⁴He concentrations and reflect the effect of degassing during atmospheric entry. Jarosite, an aqueous alteration product, is detected for 4 AMMs, indicating the aqueous alteration during long‐time storage in Antarctic ice. Jarosite‐bearing AMMs have relatively low concentrations of 4He, which is suggestive of loss during the alteration. High ³He/⁴He ratios are detected for AMMs with high ²⁰Ne/⁴He ratios, showing both cosmogenic ³He and preferential He loss. SEP (solar energetic particles)‐He and Ne, rather than the solar wind (SW), were dominant in AMMs, presumably showing a preferential removal of the more shallowly implanted SW by atmospheric entry heating. The mean ²⁰Ne/²²Ne ratio is 11.27 ± 0.35, which is close to the SEP value of 11.2. Cosmogenic ²¹Ne is not detected in any of the particles, which is probably due to the short cosmic ray exposure ages. Ar isotopic compositions are explained by 3‐component mixing of air, Q, and SEP‐Ar. Ar isotopic compositions can not be explained without significant contributions of Q‐Ar. SEP‐Ne contributed more than 99% of the total Ne. As for ³⁶Ar and ³⁸Ar, the abundance of the Q component is comparable to that of the SEP component. ⁸⁴Kr and ¹³²Xe are dominated by the primordial component, and solar‐derived Xe is almost negligible.     

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 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.     

Upper limit concentrations of trapped xenon in individual interplanetary dust particles from the stratosphere

Abstract— The Xe contents in 25 individual stratospheric interplanetary dust particles were measured in two different laboratories using focused laser micro‐gas extraction and (1) a conventional low‐blank magnetic sector mass spectrometer (Washington University), and (2) a resonance ionization time of flight mass spectrometer (RELAX‐University of Manchester). Data from both laboratories yielded a remarkably similar upper‐limit ¹³²Xe concentration in the IDPs (>2.7, 6.8 and 2.2 × 10^?8ccSTP/g for Washington University Run 1, Washington University Run 2 and University of Manchester analyses, respectively), which is up to a factor of five smaller than previous estimates. The upper‐limit ¹³²Xe/³⁶Ar ratio in the IDPs (¹³²Xe/³⁶Ar > ?8 × 10^?4for Run 1 and ¹³²Xe/³⁶Ar > ?19 × 10^?4for Run 2), computed using ³⁶Ar concentration data reported elsewhere is consistent with a mixture between implanted solar wind, primordial, and atmospheric noble gases. Most significantly, there is no evidence that IDPs are particularly enriched in primordial noble gases compared to chondritic meteorites, as implied by previous work.     

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 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.     

Cosmogenic and trapped noble gases in individual chondrules: Clues to chondrule formation

Abstract— We studied the elemental and isotopic abundances of noble gases (He, Ne, Ar in most cases, and Kr, Xe also in some cases) in individual chondrules separated from six ordinary, two enstatite, and two carbonaceous chondrites. Most chondrules show detectable amounts of trapped ²⁰Ne and ³⁶Ar, and the ratio (³⁶Ar/²⁰Ne)_t (from ordinary and carbonaceous chondrites) suggests that HL and Q are the two major trapped components. A different trend between (³⁶Ar/²⁰Ne)_t and trapped ³⁶Ar is observed for chondrules in enstatite chondrites indicating a different environment and/or mechanism for their formation compared to chondrules in ordinary and carbonaceous chondrites. We found that a chondrule from Dhajala chondrite (DH‐11) shows the presence of solar‐type noble gases, as suggested by the (³⁶Ar/²⁰Ne)_t ratio, Ne‐isotopic composition, and excess of ⁴He. Cosmic‐ray exposure (CRE) ages of most chondrules are similar to their host chondrites. A few chondrules show higher CRE age compared to their host, suggesting that some chondrules and/or precursors of chondrules have received cosmic ray irradiation before accreting to their parent body. Among these chondrules, DH‐11 (with solar trapped gases) and a chondrule from Murray chondrite (MRY‐1) also have lower values of (²¹Ne/²²Ne)_c, indicative of SCR contribution. However, such evidences are sporadic and indicate that chondrule formation event may have erased such excess irradiation records by solar wind and SCR in most chondrules. These results support the nebular environment for chondrule formation.     

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 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.     

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.     

Noble gases in chondrules and associated metal‐sulfide‐rich samples: Clues on chondrule formation and the behavior of noble gas carrier phases

Abstract— Chondrules are generally believed to have lost most or all of their trapped noble gases during their formation. We tested this assumption by measuring He, Ne, and Ar in chondrules of the carbonaceous chondrites Allende (CV3), Leoville (CV3), Renazzo (CR2), and the ordinary chondrites Semarkona (LL3.0), Bishunpur (LL3.1), and Krymka (LL3.1). Additionally, metalsulfide‐rich chondrule coatings were measured that probably formed from chondrule metal. Low primordial ²⁰Ne concentrations are present in some chondrules, while even most of them contain small amounts of primordial ³⁶Ar. Our preferred interpretation is that‐in contrast to CAIs‐the heating of the chondrule precursor during chondrule formation was not intense enough to expel primordial noble gases quantitatively. Those chondrules containing both primordial ²⁰Ne and ³⁶Ar show low presolar‐diamond‐like ³⁶Ar/²⁰Ne ratios. In contrast, the metal‐sulfide‐rich coatings generally show higher gas concentrations and Q‐like ³⁶Ar/²⁰Ne ratios. We propose that during metalsilicate fractionation in the course of chondrule formation, the Ar‐carrying phase Q became enriched in the metal‐sulfide‐rich chondrule coatings. In the silicate chondrule interior, only the most stable Ne‐carrying presolar diamonds survived the melting event leading to the low observed ³⁶Ar/²⁰Ne ratios. The chondrules studied here do not show evidence for substantial amounts of fractionated solar‐type noble gases from a strong solar wind irradiation of the chondrule precursor material as postulated by others for the chondrules of an enstatite chondrite.     

The antiquity indicator argon‐40/argon‐36 for lunar surface samples calibrated by uranium‐235‐xenon‐136 dating

Abstract— Several solar gas rich lunar soils and breccias have trapped ⁴⁰Ar/³⁶Ar ratios >10, although solar Ar is expected to yield a ratio of <0.01. Radiogenic ⁴⁰Ar produced in the lunar crust from ⁴⁰K decay was outgassed into the lunar atmosphere, ionized, accelerated in the electromagnetic field of the solar wind, and reimplanted into lunar surface material. The ⁴⁰Ar loss rate depends on the decreasing abundance of ⁴⁰K. In order to calibrate the time dependence of the ⁴⁰Ar/³⁶Ar ratio in lunar surface material, the period of reimplantation of lunar atmospheric ions and of solar wind Ar was determined using the ²³⁵U‐¹³⁶Xe dating method that relies on secondary cosmic‐ray neutron‐induced fission of ²³⁵U. We identified the trapped, fissiogenic, and cosmogenic noble gases in lunar breccia 14307 and lunar soils 70001‐8, 70181, 74261, and 75081. Uranium and Th concentrations were determined in the 74261 soil for which we obtain the ²³⁵U‐¹³⁶Xe time of implantation of 3.25^+0.38_‐0.60 Ga ago. On the basis of several cosmogenic noble gas signatures we calculate the duration of this near surface exposure of 393 ± 45 Ma and an average shielding depth below the lunar surface of 73 ± 7 g/cm². A second, recent exposure to solar and cosmic‐ray particles occurred after this soil was excavated from Shorty crater 17.2 ± 1.4 Ma ago. Using a compilation of all lunar data with reliable trapped Ar isotopic ratios and pre‐exposure times we infer a calibration curve of implantation times, based on the trapped⁴⁰ Ar/³⁶Ar ratio. A possible trend for the increase with time of the solar ³He/⁴He and ²⁰Ne/²²Ne ratios of about 12%/Ga and about 2%/Ga, respectively, is also discussed.     

Evidence for common breakup events of the acapulcoites‐lodranites and chondrites

Abstract— Acapulcoites and lodranites are believed to originate on a common parent body and to represent some of the earliest events in the differentiation of the chondritic asteroids. We have conducted isotopic studies of the noble gases He, Ne, Ar, Kr, and Xe, and determinations of the concentrations of the major elements and of the radionuclides ¹⁰Be, ²⁶Al, and ³⁶Cl in an attempt to constrain the cosmic‐ray exposure history of two members of the acapulcoite‐lodranite clan recovered in Antarctica: Frontier Mountain (FRO) 95029 and Graves Nunataks (GRA) 95209. From cosmic‐ray‐produced ³He, ²¹Ne, and ³⁸Ar and appropriate production rates, we derive parent‐body breakup times of 4.59 ± 0.60 and 6.82 ± 0.60 Ma for FOR 95029 and GRA 95209, respectively. These times are consistent with those obtained from the pairs ¹⁰Be‐²¹Ne and ²⁶Al‐²¹Ne; whereas the times inferred from the pair ³⁶Cl‐³⁶Ar are slightly longer, perhaps because the ³⁶Cl activities decreased as a result of decay on Earth. Terrestrial ages up to ～50 ka for the two meteorites are consistent with the measured ³⁶Cl activities of the metal phases. All acapulcoites and lodranites dated until now show cosmic‐ray exposure ages in the range of 4–10 Ma. This is the same range as that found for the major exposure age cluster of the H chondrites. As a common parent body is improbable on the basis of the O‐isotopic systematics, a common set of impactors might have affected the asteroid belt 4–10 Ma ago.     

Solar wind noble gases and nitrogen in metal from lunar soil 68501

Abstract Noble gases and N were analyzed in handpicked metal separates from lunar soil 68501 by a combination of step-wise combustions and pyrolyses. Helium and Ne were found to be unfractionated with respect to one another when normalized to solar abundances, for both the bulk sample and for all but the highest temperature steps. However, they are depleted relative to Ar, Kr and Xe by at least a factor of 5. The heavier gases exhibit mass-dependent fractionation relative to solar system abundance ratios but appear unfractionated, both in the bulk metal and in early temperature steps, when compared to relative abundances derived from lunar ilmenite 71501 by chemical etching, recently put forward as representing the abundance ratios in solar wind. Estimates of the contribution of solar energetic particles (SEP) to the originally implanted solar gases, derived from a basic interpretation of He and Ne isotopes, yield values of about 10%. Analysis of the Ar isotopes requires a minimum of 20% SEP, and Kr isotopes, using our preferred composition for solar wind Kr, yield a result that overlaps both of these values. It is possible to reconcile the data from these gases if significant loss of solar wind Ar, Kr and presumably Xe has occurred relative to the SEP component, most likely by erosive processes that are mass independent, although mass-dependent losses (Ar > Kr > Xe) cannot be excluded. If such losses did occur, the SEP contribution to the solar implanted gases must have been no more than a few percent. Nitrogen is a mixture of indigenous meteoritic N, whose isotopic composition is inferred to be relatively light, and implanted solar N, which has probably undergone diffusive redistribution and fractionation. If the heavy noble gases have not undergone diffusive loss, then N/Ar in the solar wind can be inferred to be at least several times the accepted solar ratio. The solar wind N appears, even after correction for fractionation effects, to have a minimum δ¹⁵N value ≥+150‰ and a more probable value ≥+200‰.     

Effects of experimental aqueous alteration on the abundances of argon‐rich noble gases in the Ningqiang carbonaceous chondrite

Abstract— Ar‐rich noble gases, the so‐called “subsolar” noble gases, are a major component of heavy primordial noble gases in unequilibrated ordinary chondrites and some classes of anhydrous carbonaceous chondrites, whereas they are almost absent in hydrous carbonaceous chondrites that suffered extensive aqueous alteration. To understand the effects of aqueous alteration on the abundance of Ar‐rich noble gases, we performed an aqueous alteration experiments on the Ningqiang type 3 carbonaceous chondrite that consists entirely of anhydrous minerals and contains Ar‐rich noble gases. Powdered samples and deionized neutral water were kept at 200 °C for 10 and 20 days, respectively. Mineralogical analyses show that, during the 10‐day alteration, serpentine and hematite formed at the expense of olivine, low‐Ca pyroxene, and sulfide. Noble gas analyses show that the 10‐day alteration of natural Ningqiang removed 79% of the primordial ³⁶Ar, 68% of the ⁸⁴Kr, and 60% of the ¹³²Xe, but only 45% of the ⁴He and 53% of the primordial ²⁰Ne. Calculated elemental ratios of the noble gases removed during the 10‐day alteration are in the range of those of Ar‐rich noble gases. These results indicate that Ar‐rich noble gases are located in materials that are very susceptible to aqueous alteration. In contrast, heavy primordial noble gases remaining in the altered samples are close to Q gas in elemental and isotope compositions. This indicates that phase Q is much more resistant to aqueous alteration than the host phases of Ar‐rich noble gases. In the 20‐day sample, the mineralogical and noble gas signatures are basically similar to those of the 10‐day sample, indicating that the loss of Ar‐rich noble gases was completed within the 10‐day alteration. Our results suggest that almost all of the Ar‐rich noble gases were lost from primitive asteroids during early, low‐temperature aqueous alteration.     

Effects of aqueous alteration on primordial noble gases and presolar SiC in the carbonaceous chondrite Tagish Lake

Effects of aqueous alteration on primordial noble gas carriers were investigated by analyzing noble gases and determining presolar SiC abundances in insoluble organic matter (IOM) from four Tagish Lake meteorite (C2‐ung.) samples that experienced different degrees of aqueous alteration. The samples contained a mixture of primordial noble gases from phase Q and presolar nanodiamonds (HL, P3), SiC (Ne‐E[H]), and graphite (Ne‐E[L]). The second most altered sample (11i) had a ~2–3 times higher Ne‐E concentration than the other samples. The presolar SiC abundances in the samples were determined from NanoSIMS ion images and 11i had a SiC abundance twice that of the other samples. The heterogeneous distribution of SiC grains could be inherited from heterogeneous accretion or parent body alteration could have redistributed SiC grains. Closed system step etching (CSSE) was used to study noble gases in HNO₃‐susceptible phases in the most and least altered samples. All Ne‐E carried by presolar SiC grains in the most altered sample was released during CSSE, while only a fraction of the Ne‐E was released from the least altered sample. This increased susceptibility to HNO₃ likely represents a step toward degassing. Presolar graphite appears to have been partially degassed during aqueous alteration. Differences in the ⁴He/³⁶Ar and ²⁰Ne/³⁶Ar ratios in gases released during CSSE could be due to gas release from presolar nanodiamonds, with more He and Ne being released in the more aqueously altered sample. Aqueous alteration changes the properties of presolar grains so that they react similar to phase Q in the laboratory, thereby altering the perceived composition of Q.     

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.     

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.     

Similarities and differences between the solar wind light noble gas compositions determined on Apollo 15 SWC foils and on NASA Genesis targets

We compare the solar wind (SW) He, Ne, and Ar compositions collected during the Apollo Solar Wind Composition (SWC) experiments (1969–1972; Al‐ & Pt‐foils) and the Genesis mission (2002–2004; so‐called DOS targets considered here). While published SW ²⁰Ne/²²Ne and ³⁶Ar/³⁸Ar ratios of both data sets agree, differences exist in the ⁴He/³He, ⁴He/²⁰Ne, and ²⁰Ne/³⁶Ar ratios. However, ²⁰Ne/³⁶Ar ratios from Apollo‐16 Pt‐foils, exclusively adopted as SW values by the SWC team, are consistent with the Genesis results. We investigate if the differences indicate a variability of the SW over the course of about 30 yr, or systematic biases of the two data sets, which were collected in different environments and measured several decades apart in different laboratories (University of Bern; ETH Zurich). New measurements of Apollo‐15 SWC aluminum foils in Zurich generally agree with the original measurements performed in Bern. Zurich samples show slightly lower ⁴He concentrations suggesting a few percent of diffusive loss of ⁴He during storage of the foils. A 3% difference between the He isotopic ratios measured in Bern and in Zurich possibly represents an analytical bias between the laboratories. The low SW ⁴He/²⁰Ne and ²⁰Ne/³⁶Ar ratios in Apollo‐15 Al‐foils compared to Genesis data are consistent with a mixture of Genesis‐like SW and noble gases from small amounts of lunar dust. Our data suggest that the mean SW He, Ne, and Ar isotopic and elemental compositions have not significantly changed between the overall Apollo and Genesis mission collection periods.     

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.