Geochemistry of the ungrouped carbonaceous chondrite Tagish Lake,the anomalous CM chondrite Bells,and comparison with CI and CM chondrites

Abstract— I have determined the composition via instrumental neutron activation analysis of a bulk pristine sample of the Tagish Lake carbonaceous chondrite fall, along with bulk samples of the CI chondrite Orgueil and of several CM chondrites. Tagish Lake has a mean of refractory lithophile element/Cr ratios like those of CM chondrites, and distinctly higher than the CI chondrite mean. Tagish Lake exhibits abundances of the moderately volatile lithophile elements Na and K that are slightly higher than those of mean CM chondrites. Refractory through moderately volatile siderophile element abundances in Tagish Lake are like those of CM chondrites. Tagish Lake is distinct from CM chondrites in abundances of the most volatile elements. Mean CI‐normalized Se/Co, Zn/Co and Cs/Co for Tagish Lake are 0.68 ± 0.01, 0.71 ± 0.07 and 0.76 ± 0.02, while for all available CM chondrite determinations, these ratios lie between 0.31 and 0.61, between 0.32 and 0.58, and between 0.39 and 0.74, respectively. Considering petrography, and oxygen isotopic and elemental compositions, Tagish Lake is an ungrouped member of the carbonaceous chondrite clan. The overall abundance pattern is similar to those of CM chondrites, indicating that Tagish Lake and CMs experienced very similar nebular fractionations. Bells is a CM chondrite with unusual petrologic characteristics. Bells has a mean CI‐normalized refractory lithophile element/Cr ratio of 0.96, lower than for any other CM chondrite, but shows CI‐normalized moderately volatile lithophile element/Cr ratios within the ranges of other CM chondrites, except for Na which is low. Iridium, Co, Ni and Fe abundances are like those of CM chondrites, but the moderately volatile siderophile elements, Au, As and Sb, have abundances below the ranges for CM chondrites. Abundances of the moderately volatile elements Se and Zn of Bells are within the CM ranges. Bells is best classified as an anomalous CM chondrite.     

The Kumtag 016 L5 strewn field,Xinjiang Province,China

The Kumtag 016 strewn field was found in the eastern part of the Kumtag desert, Xinjiang Province, China. In this study, 24 recovered meteorites have been characterized by a suite of different analytical techniques to investigate their petrography, mineralogy, bulk trace elements, noble gas isotopic composition, density, and porosity. We attribute to the strewn field 22 L5 chondrites with shock stage S4 and weathering grade W2–W3. Two different meteorites, Kumtag 021, an L4 chondrite and Kumtag 032, an L6 chondrite, were recognized within the strewn field area. Moreover, Kumtag 003, an H5 chondrite, was previously found in the same area. We infer that the Kumtag 016 strewn field most likely consists of at least four distinct meteorite falls. The effects of terrestrial weathering on the studied meteorites involve sulfide/metal alteration, chemical changes (Sr, Ba, Pb, and U enrichments and depletion in Cr, Co, Ni, and Cs abundances), and physical modifications (decrease of grain density and porosity). Measurements of the light noble gases indicate that the analyzed Kumtag L5 samples contain solar wind-implanted noble gases with a ²⁰Ne/²²Ne ratio of ~12.345. The cosmic-ray exposure (CRE) ages of the L5 chondrites are in a narrow range (3.6 ± 1.4 Ma to 5.2 ± 0.4 Ma). For L4 chondrite Kumtag 021 and L6 chondrite Kumtag 032, the CRE ages are 5.9 ± 0.4 Ma and 4.7 ± 0.8 Ma, respectively.     

Noble gas record,collisional history,and pairing of CV,CO, CK,and other carbonaceous chondrites

Abstract— Concentration and isotopic composition of the light noble gases as well as of ⁸⁴Kr, ¹²⁹Xe, and ¹³²Xe have been measured in bulk samples of 60 carbonaceous chondrites; 45 were measured for the first time. Solar noble gases were found in nine specimens (Arch, Acfer 094, Dar al Gani 056, Graves Nunataks 95229, Grosnaja, Isna, Mt. Prestrud 95404, Yamato (Y) 86009, and Y 86751). These meteorites are thus regolith breccias. The CV and CO chondrites contain abundant planetary‐type noble gases, but not CK chondrites. Characteristic features of CK chondrites are high ¹²⁹Xe/¹³²Xe ratios. The petrologic type of carbonaceous chondrites is correlated with the concentration of trapped heavy noble gases, similar to observations shown for ordinary chondrites. However, this correlation is disturbed for several meteorites due to a contribution of atmospheric noble gases, an effect correlated to terrestrial weathering effects. Cosmic‐ray exposure ages are calculated from cosmogenic ²¹Ne. They range from about 1 to 63.5 Ma for CO, CV, and CK classes, which is longer than exposure ages reported for CM and CI chondrites. Only the CO3 chondrite Isna has an exceptionally low exposure age of 0.15 Ma. No dominant clusters are observed in the cosmic‐ray exposure age distribution; only for CV and CK chondrites do potential peaks seem to develop at ～9 and ～29 Ma. Several pairings among the chondrites from hot deserts are suggested, but 52 of the 60 investigated meteorites are individual falls. In general, we confirm the results of Mazor et al. (1970) regarding cosmic‐ray exposure and trapped heavy noble gases. With this study, a considerable number of new carbonaceous chondrites were added to the noble gas data base, but this is still not sufficient to obtain a clear picture of the collisional history of the carbonaceous chondrite groups. Obviously, the exposure histories of CI and CM chondrites differ from those of CV, CO, and CK chondrites that have much longer exposure ages. The close relationship among the latter three is also evident from the similar cosmic‐ray exposure age patterns that do not reveal a clear picture of major breakup events. The CK chondrites, however, with their wide range of petrologic types, form the only carbonaceous chondrite group which so far lacks a solar‐gas‐bearing regolith breccia. The CK chondrites contain only minute amounts of trapped noble gases and their noble gas fingerprint is thus distinguishable from the other groups. In the future, more analyses of newly collected CK chondrites are needed to unravel the genetic and historic evolution of this group. It is also evident that the problems of weathering and pairing have to be considered when noble gas data of carbonaceous chondrite are interpreted.     

Mineralogy and chemistry of Rumuruti: The first meteorite fall of the new R chondrite group

Abstract— The Rumuruti meteorite shower fell in Rumuruti, Kenya, on 1934 January 28 at 10:43 p.m. Rumuruti is an olivine-rich chondritic breccia with light-dark structure. Based on the coexistence of highly recrystallized fragments and unequilibrated components, Rumuruti is classified as a type 3–6 chondrite breccia. The most abundant phase of Rumuruti is olivine (mostly Fa_～39) with about 70 vol%. Feldspar (～14 vol%; mainly plagioclase), Ca-pyroxene (5 vol%), pyrrhotite (4.4 vol%), and pentlandite (3.6 vol%) are major constituents. All other phases have abundances below 1 vol%, including low-Ca pyroxene, chrome spinels, phosphates (chlorapatite and whitlockite), chalcopyrite, ilmenite, tridymite, Ni-rich and Ge-containing metals, kamacite, and various particles enriched in noble metals like Pt, Ir, arid Au. The chemical composition of Rumuruti is chondritic. The depletion in refractory elements (Sc, REE, etc.) and the comparatively high Mn, Na, and K contents are characteristic of ordinary chondrites and distinguish Rumuruti from carbonaceous chondrites. However, S, Se, and Zn contents in Rumuruti are significantly above the level expected for ordinary chondrites. The oxygen isotope composition of Rumuruti is high in δ¹⁷O (5.52 ‰) and δ¹⁸O (5.07 ‰). Previously, a small number of chondritic meteorites with strong similarities to Rumuruti were described. They were called Carlisle Lakes-type chondrites and they comprise: Carlisle Lakes, ALH85151, Y-75302, Y-793575, Y-82002, Acfer 217, PCA91002, and PCA91241, as well as clasts in the Weatherford chondrite. All these meteorites are finds from hot and cold deserts having experienced various degrees of weathering. With Rumuruti, the first meteorite fall has been recognized that preserves the primary mineralogical and chemical characteristics of a new group of meteorites. Comparing all chondrites, the characteristic features can be summarized as follows: (a) basically chondritic chemistry with ordinary chondrite element patterns of refractory and moderately volatile lithophiles but higher abundances of S, Se, and Zn; (b) high degree of oxidation (37–41 mol% Fa in olivine, only traces of Fe, Ni-metals, occurrence of chalcopyrite); (c) exceptionally high Δ¹⁷O values of about 2.7 for bulk samples; (d) high modal abundance of olivine (～70 vol%); (e) Ti-Fe³⁺?rich chromite (～5.5 wt% TiO₂); (f) occurrence of various noble metal-rich particles; (g) abundant chondritic breccias consisting of equilibrated clasts and unequilibrated lithologies. With Rumuruti, nine meteorite samples exist that are chemically and mineralogically very similar. These meteorites are attributed to at least eight different fall events. It is proposed in this paper to call this group R chondrites (rumurutiites) after the first and only fall among these meteorites. These meteorites have a close relationship to ordinary chondrites. However, they are more oxidized than any of the existing groups of ordinary chondrites. Small, but significant differences in chemical composition and in oxygen isotopes between R chondrites and ordinary chondrites exclude formation of R chondrites from ordinary chondrites by oxidation. This implies a separate, independent R chondrite parent body.     

Guangnan (L6) and Ningqiang (CV3): Exposure Ages and Radiogenic Ages of Two Unusual Chondrites

Abstract— The isotopic abundances of the noble gases in bulk samples of the Guangnan L6 chondrite and of the anomalous CV3 chondrite Ningqiang were measured. Guangnan yields a cosmic-ray exposure age of 2.9 ± 0.4 Ma and belongs to the group of L chondrites with low exposure ages. Ningqiang, however, shows a cosmic-ray exposure age of 42.2 ± 4.0 Ma, the highest for a CV3 chondrite. The concentrations of radiogenic ⁴He and ⁴⁰Ar in Guangnan are the lowest observed in any ordinary chondrite. A U/Th-⁴He age of 27 ± 16 Ma and a ⁴⁰K–⁴⁰Ar age of 142 ± 14 Ma are calculated assuming L chondritic U, Th, and K concentrations. This assumption is justified considering the fact that a mineralogical composition typical for L chondrites was reported for this meteorite. The observed severe gas losses must have occurred at or before the onset of the exposure of the meteoroid to the cosmic radiation. For the Ningqiang carbonaceous chondrite concordant gas retention ages are obtained: The U/Th-⁴He age is 4170 ± 160 Ma whereas the ⁴⁰K–⁴⁰Ar age is 4260 ± 70 Ma, assuming average U, Th, and K concentrations for C3 chondrites.     

Cosmic‐ray exposure age and heliocentric distance of the parent bodies of enstatite chondrites ALH 85119 and MAC 88136

Abstract— We measured concentrations and isotopic ratios of noble gases in enstatite (E) chondrites Allan Hills (ALH) 85119 and MacAlpine Hills (MAC) 88136. These two meteorites contain solar and cosmogenic noble gases. Based on the solar and cosmogenic noble gas compositions, we calculated heliocentric distances, parent body exposure ages, and space exposure ages of the two meteorites. The parent body exposure ages are longer than 6.7 Ma for ALH 85119 and longer than 8.7 Ma for MAC 88136. The space exposure ages are shorter than 2.2 Ma for ALH 85119 and shorter than 3.9 Ma for MAC 88136. The estimated heliocentric distances are more than 1.1 AU for ALH 85119 and 1.3 AU for MAC 88136. Derived heliocentric distances indicate the locations of parent bodies in the past when constituents of the meteorites were exposed to the Sun. From the mineralogy and chemistry of E chondrites, it is believed that E chondrites formed in regions within 1.4 AU from the Sun. The heliocentric distances of the two E chondrite parent bodies are not different from the formation regions of E chondrites. This may imply that heliocentric distances of E chondrites have been relatively constant from their formation stage to the stage of exposure to the solar wind.     

Coolidge and Loongana 001: A new carbonaceous chondrite grouplet

Abstract— Petrographic and bulk compositional data suggest the existence of a new grouplet of carbonaceous chondrites consisting of Coolidge and Loongana 001. Coolidge is a carbonaceous chondrite find from Kansas, USA, previously considered a metamorphosed CV chondrite. Loongana 001 is a recent find from Western Australia. It has a high matrix/chondrule modal abundance ratio, 1–2 vol% refractory inclusions and high refractory lithophile abundance ratios (～1.35x CI), indicating that it is a carbonaceous chondrite. Coolidge and Loongana 001 have many compositional and petrographic similarities. They have refractory element abundances in the range of CV chondrites, significantly higher than those in the CR chondrites. They have similar volatile element abundance patterns showing low volatile element abundances relative to both CR and CV chondrites. Coolidge and Loongana 001 have similar chondrule dimensions and shapes, oxidation states and opaque mineral assemblages. They are also similar in petrologic type (3.8–4) and shock stage (S2). Although both Coolidge and Loongana 001 may be related to the CV clan, they are not CV chondrites, nor are they formed by metamorphism of a CV precursor. They are distinctly different in composition from CV chondrites and their chondrules are smaller and have a much lower abundance of coarse-grained chondrule rims. Coolidge and Loongana 001 constitute a distinct carbonaceous chondrite grouplet.     

Chemical variations of sulfides and metal in enstatite chondrites—Introduction of a new classification scheme

In this study, the metal and sulfide compositions of 45 enstatite chondrites were analyzed to determine possible mineral-chemical trends correlated with the petrologic type. Data for 35 additional samples were taken from the literature. Considering the data from this huge number of different E chondrite samples (80 in total), none of the trends previously described in the literature could be clearly confirmed. Also, among the opaque phases of enstatite chondrites, no other “new” correlations between mineral chemistry and the petrologic type were found. However, major differences in the sulfide and metal chemistry became obvious. Specifically, a certain number of chondrites in the EH and the EL groups have Cr in troilite above 2 wt%, Fe in niningerite or alabandite above 20 wt%, and lack abundant daubréelite. Differences were also found for Ni concentrations in kamacite. Thus, we propose a system for classifying E chondrites by defining four major subgroups: EH_a, EL_a, EH_b, and EL_b. All subgroups show full petrologic sequences that are similar to each other. This observation, in combination with the differences in sulfide and metal chemistry, suggests an origin of the samples from different parent bodies. Considering the anomalous E chondrite samples that neither fit in the previous classification scheme nor in the new one described here, the samples investigated in this study require at least eight different parent bodies.     

Mineralogy and 57Fe Mössbauer spectroscopy of opaque phases in the Neuschwanstein EL6 chondrite

Abstract— This study presents compositional data and ⁵⁷Fe Mössbauer spectra, taken at 295 K and 85 K, of two fragments of the enstatite (EL6) chondrite Neuschwanstein that fell near the famous Neuschwanstein castle (Bavaria, southern Germany) on April 6, 2002. Main silicate minerals are enstatite (Fs 2) and plagioclase (An 20), the main opaque minerals are kamacite and troilite. Small amounts of oldhamite, daubreelite, and schreibersite have been found. The presented Mössbauer data are the first data gathered for an EL6 chondrite. The dominant parts of each Mössbauer spectrum consist of two six‐line patterns due to the presence of ferromagnetic phases kamacite and troilite. In contrast to other chondrites, peaks of other iron species in the central parts of the spectra are missing due to an extremely low content of Fe‐bearing paramagnetic components. The hyperfine interaction parameters for kamacite are internal magnetic hyperfine field H_hf = 333.2 kOe, isomer shift (relative to a metallic Fe foil) IS = 0.01 mm/s, quadrupole splitting QS = 0 mm/s, line width W = 0.41 mm/s. The data for troilite are H_hf = 305.5 kOe, IS = 0.75 mm/s, QS = ?0.85 mm/s, W = 0.34 mm/s.     

Roosevelt County 075: A petrologic,chemical and isotopic study of the most unequilibrated known H chondrite

Abstract— Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite, δ¹³C). Petrologic subtype 3.2± 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most unequilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.     

Petrogenesis of anomalous Queen Alexandra Range enstatite meteorites and their relation to enstatite chondrites,primitive enstatite achondrites,and aubrites

Queen Alexandra Range (QUE) meteorite 94204 is an anomalous enstatite meteorite whose petrogenesis has been ascribed to either partial melting or impact melting. We studied the meteorite pairs QUE 94204, 97289/97348, 99059/99122/99157/99158/99387, and Yamato (Y)‐793225; these were previously suggested to represent a new grouplet. We present new data for mineral abundances, mineral chemistries, and siderophile trace element compositions (of Fe,Ni metal) in these meteorites. We find that the texture and composition of Y‐793225 are related to EL6, and that this meteorite is unrelated to the QUEs. The mineralogy and siderophile element compositions of the QUEs are consistent with petrogenesis from an enstatite chondrite precursor. We caution that potential re‐equilibration during melting and recrystallization of enstatite chondrite melt‐rocks make it unreliable to use mineral chemistries to assign a specific parent body affinity (i.e., EH or EL). The QUEs have similar mineral chemistries among themselves, while slight variations in texture and modal abundances exist between them. They are dominated by inclusion‐bearing millimeter‐sized enstatite (average En_99.1–99.5) with interstitial spaces filled predominantly by oligoclase feldspar (sometimes zoned), kamacite (Si approximately 2.4 wt%), troilite (≤2.4 wt% Ti), and cristobalite. Siderophile elements that partition compatibly between solid metal and liquid metal are not enriched like in partial melt residues Itqiy and Northwest Africa (NWA) 2526. We find that the modal compositions of the QUEs are broadly unfractionated with respect to enstatite chondrites. We conclude that a petrogenesis by impact melting, not partial melting, is most consistent with our observations.     

QUE 94204: A primitive enstatite achondrite produced by the partial melting of an E chondrite‐like protolith

Abstract– Queen Alexandra Range (QUE) 94204, an enstatite achondrite, is a coarse‐grained, highly recrystallized, chondrule‐free and unbrecciated rock dominated (about 70 vol%) by anhedral, equigranular crystals of orthoenstatite of nearly endmember composition (Fs_0.1–0.4, Wo_0.3–0.4) with interstitial plagioclase, kamacite, and troilite. Abundance of approximately 120° triple junctions and the close association of metal–sulfide and plagioclase‐rich melts indicate that QUE 94204 has undergone limited partial melting with inefficient melt extraction. Mineral chemistry indicates a high degree of thermal metamorphism. Kamacite in QUE 94204 contains between 2.09 and 2.55 wt% Si, similar to highly metamorphosed EL chondrites. Plagioclase has between 4.31 and 6.66 wt% CaO, higher than other E chondrites but closer in composition to plagioclase from metamorphosed EL chondrites. QUE 94204 troilite contains up to 2.55 wt% Ti, consistent with extensive thermal metamorphism of an E chondrite‐like precursor. Results presented in this study indicate that QUE 94204 is the result of low degree, (about 5–20 vol%, probably toward the lower end of this range) partial melting of an E chondrite protolith. Textural and chemical evidence suggests that during the metamorphism of QUE 94204, melts formed first at the Fe,Ni‐FeS cotectic near approximately 900 °C, followed by plagioclase‐pyroxene silicate partial melts near approximately 1100 °C. Neither the Fe,Ni‐FeS nor the plagioclase‐pyroxene melts were efficiently segregated or extracted. QUE 94204 belongs to a grouplet of similar “primitive enstatite achondrites” that are analogous to the acapulcoites‐lodranites, but that have resulted from the partial melting of an E chondrite‐like protolith.     

Terrestrial ages,pairing, and concentration mechanism of Antarctic chondrites from Frontier Mountain,Northern Victoria Land

Abstract— We report concentrations of cosmogenic ¹⁰Be, ²⁶Al, ³⁶Cl, and ⁴¹Ca in the metal phase of 26 ordinary chondrites from Frontier Mountain (FRO), Antarctica, as well as cosmogenic ¹⁴C in eight and noble gases in four bulk samples. Thirteen out of 14 selected H chondrites belong to two previously identified pairing groups, FRO 90001 and FRO 90174, with terrestrial ages of ?40 and ?100 kyr, respectively. The FRO 90174 shower is a heterogeneous H3–6 chondrite breccia that probably includes more than 300 individual fragments, explaining the high H/L chondrite ratio (3.8) at Frontier Mountain. The geographic distribution of 19 fragments of this shower constrains ice fluctuations over the past 50–100 kyr to less than ?40 m, supporting the stability of the meteorite trap over the last glacial cycle. The second H‐chondrite pairing group, FRO 90001, is much smaller and its geographic distribution is mainly controlled by wind‐transport. Most L‐chondrites are younger than 50 kyr, except for the FRO 93009/01172 pair, which has a terrestrial age of ?500 kyr. These two old L chondrites represent the only surviving members of a large shower with a similar preatmospheric radius (?80 cm) as the FRO 90174 shower. The find locations of these two paired L‐chondrite fragments on opposite sides of Frontier Mountain confirm the general glaciological model in which the two ice flows passing both ends of the mountain are derived from the same source area on the plateau. The 50 FRO meteorites analyzed so far represent 21 different falls. The terrestrial ages range from 6 kyr to 500 kyr, supporting the earlier proposed concentration mechanism.     

Origin of Halogens and Nitrogen in Enstatite Chondrites

The EH and EL enstatite chondrites are the most reduced chondrite groups, having formed in nebular regions where the gas may have had high C/O and/or pH₂/pH₂O ratios. Enstatite chondrites (particularly EH) have higher CI- and Mg-normalized abundances of halogens (especially F and Cl) and nitrogen than ordinary chondrites and most groups of carbonaceous chondrites. Even relative to CI chondrites, EH and EL chondrites are enriched in F. We have found that literature values for the halogen abundance ratios in EH and EL chondrites are strongly correlated with the electronegativities of the individual halogens. We suggest that the most reactive halogens were the most efficient at forming compounds (e.g., halides) that were incorporated into EH-chondrite precursor materials. It seems plausible that, under the more-oxidizing conditions pertaining to the other chondrite groups, a larger fraction of the halogens remained in the gas. Nitrogen may have been incorporated into the enstatite chondrites as simple nitrides that did not condense under the more-oxidizing conditions in the regions where other chondrite groups formed. Literature data show that unequilibrated enstatite chondrites have light bulk N (δ ¹⁵N ≈ −20‰) compared to most ordinary (−5 to +20‰) and carbonaceous (+20 to +190‰) chondrites; this may reflect the contribution in enstatite chondrites of nitride condensates with δ¹⁵ N values close to the proposed nebular mean (~−400‰). In contrast, N in carbonaceous chondrites is mainly contained within ¹⁵N-rich organic matter. The major carrier of N in ordinary chondrites is unknown.     

Thermal history of the enstatite chondrites from silica polymorphs

Abstract— Here we report the results of our petrologic and mineralogical study of enstatite (E) chondrites in order to explore their thermal histories. We studied silica phases in 20 E chondrites by laser micro Raman spectroscopy to determine the silica polymorphs they contain. Silica phases are commonly present in E chondrites and their polymorphs reflect the physical conditions of formation. The samples studied here include EH3–5, EL3–6, E chondrite melt rocks, and an anomalous E chondrite. We identified quartz, tridymite, cristobalite, and silica glass in the samples studied. EH4–5 and EH melt rocks are divided into high and low temperature classes based on niningerite‐alabandite solid solutions. EH3, EL3, and some EH melt rocks of the high temperature class contain tridymite and cristobalite. We suggest that tridymite and cristobalite crystallized in chondrules and E chondrite melts, followed by rapid cooling, leading to the survival of these silica polymorphs. EH4 and EL4 chondrites also contain tridymite and cristobalite in their chondrules, indicating that these silica polymorphs survived low temperature metamorphism (as estimated from opaque mineral geothermometers) because of the sluggishness of the transition to a more stable polymorph. Tridymite and cristobalite in EL6 chondrites reflect the high temperature processes experienced by these meteorites. On the other hand, some EH5 chondrites and EH melt rocks of the low temperature class contain quartz, which may be a product of the transition from tridymite or cristobalite during a long period of low temperature metamorphism. Although the thermal history of E chondrites have been previously estimated from opaque minerals, such compositions mainly reflect low temperature processes. However, we can reconstruct the primordial thermal processes and subsequent cooling histories of E chondrites from their silica polymorphs. The E chondrites have complicated thermal histories, which produced the observed variations among them.     

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.     

Light noble gases in 12 meteorites from the Omani desert,Australia, Mauritania,Canada, and Sweden

We measured the concentrations and isotopic compositions of He, Ne, and Ar in 14 fragments from 12 different meteorites: three carbonaceous chondrites, six L chondrites (three most likely paired), one H chondrite, one R chondrite, and one ungrouped chondrite. The data obtained for the CV3 chondrites Ramlat as Sahmah (RaS) 221 and RaS 251 support the hypothesis of exposure age peaks for CV chondrites at approximately 9 Ma and 27 Ma. The exposure age for Shi?r 033 (CR chondrite) of 7.3 Ma is also indicative of a possible CR chondrite exposure age peak. The three L chondrites Jiddat al Harasis (JaH) 091, JaH 230, and JaH 296, which are most likely paired, fall together with Hallingeberg into the L chondrite exposure age peak of approximately 15 Ma. The two L chondrites Shelburne and Lake Torrens fall into the peaks at approximately 40 Ma and 5 Ma, respectively. The ages for Bassikounou (H chondrite) and RaS 201 (R chondrite) are approximately 3.5 Ma and 5.8 Ma, respectively. Six of the studied meteorites show clear evidence for ³He diffusive losses, the deficits range from approximately 17% for one Lake Torrens aliquot to approximately 45% for RaS 211. The three carbonaceous chondrites RaS 221, RaS 251, and Shi?r 033 all have excess ⁴He, either of planetary or solar origin. However, very high ⁴He/²⁰Ne ratios occur at relatively low ²⁰Ne/²²Ne ratios, which is unexpected and needs further study. The measured ⁴⁰Ar ages fit well into established systematics. They are between 2.5 and 4.5 Ga for the carbonaceous chondrites, older than 3.6 Ga for the L and H chondrites, and about 2.4 Ga for the R chondrite as well as for the ungrouped chondrite. Interestingly, none of our studied L chondrites has been degassed in the 470 Ma break‐up event. Using the amount of trapped ³⁶Ar as a proxy for noble gas contamination due to terrestrial weathering we are able to demonstrate that the samples studied here are not or only very slightly affected by terrestrial weathering (at least in terms of their noble gas budget).     

Nitrogen and noble gases in micrometeorites

Abstract— Micrometeorites (MMs) currently represent the largest steady‐state mass flux of extraterrestrial matter to Earth and may have delivered a significant fraction of volatile elements and organics to the Earth's surface. Nitrogen and noble gases contents and isotopic ratios have been measured in a suite of 17 micrometeorites recovered in Antarctica (sampled in blue ice at Cap Prudhomme) and Greenland (separated from cryoconite) that have experienced variable thermal metamorphism during atmospheric entry. MMs were pyrolized using a CO₂ laser and the released gases were analyzed for nitrogen and noble gas abundances and isotopic ratios by static mass spectrometry after specific purification. Noble gases are a mixture of cosmogenic, solar, atmospheric, and possibly chondritic components, with atmospheric being predominant in severely heated MMs. δ¹⁵N values vary between ?240 ± 62‰ and +206 ± 12‰, with most values being within the range of terrestrial and chondritic signatures, given the uncertainties. Crystalline MMs present very high noble gas contents up to two orders of magnitude higher than carbonaceous chondrite concentrations. In contrast, nitrogen contents between 4 ppm and 165 ppm are much lower than those of carbonaceous chondrites, evidencing either initially low N content in MMs and/or degradation of phases hosting nitrogen during atmospheric entry heating and terrestrial weathering. Assuming that the original N content of MMs was comparable to that of carbonaceous chondrites, the contribution of nitrogen delivery by these objects to the terrestrial environment would have been probably marginal from 3.8 Gyr ago to present but could have been significant (?10%) in the Hadean, and even predominant during the latest stages of terrestrial accretion.     

Exposure history and terrestrial ages of ordinary chondrites from the Dar al Gani region,Libya

Abstract— We measured the concentrations of noble gases in 32 ordinary chondrites from the Dar al Gani (DaG) region, Libya, as well as concentrations of the cosmogenic radionuclides ¹⁴C, ¹⁰Be, ²⁶Al, ³⁶Cl, and ⁴¹Ca in 18 of these samples. Although the trapped noble gases in five DaG samples show ratios typical of solar or planetary gases, in all other DaG samples, they are dominated by atmospheric contamination, which increases with the degree of weathering. Cosmic ray exposure (CRE) ages of DaG chondrites range from ?1 Myr to 53 Myr. The CRE age distribution of 10 DaG L chondrites shows a cluster around 40 Myr due to four members of a large L6 chondrite shower. The CRE age distribution of 19 DaG H chondrites shows only three ages coinciding with the main H chondrite peak at ?7 Myr, while seven ages are <5 Myr. Two of these H chondrites with short CRE ages (DaG 904 and 908) show evidence of a complex exposure history. Five of the H chondrites show evidence of high shielding conditions, including low ²²Ne/²¹Ne ratios and large contributions of neutron‐capture ³⁶Cl and ⁴¹Ca. These samples represent fragments of two or more large pre‐atmospheric objects, which supports the hypothesis that the high H/L chondrite ratio at DaG is due to one or more large unrecognized showers. The ¹⁴C concentrations correspond to terrestrial ages <35 kyr, similar to terrestrial ages of chondrites from other regions in the Sahara but younger than two DaG achondrites. Despite the loss of cosmogenic ³⁶Cl and ⁴¹Ca during oxidation of metal and troilite, concentrations of ³⁶Cl and ⁴¹Ca in the silicates are also consistent with ¹⁴C ages <35 kyr. The only exception is DaG 343 (H4), which has a ⁴¹Ca terrestrial age of 150 ± 40 kyr. This old age shows that not only iron meteorites and achondrites but also chondrites can survive the hot desert environment for more than 50 kyr. A possible explanation is that older meteorites were covered by soils during wetter periods and were recently exhumed by removal of these soils due to deflation during more arid periods, such as the current one, which started ?3000 years ago. Finally, based on the ²⁶Al/²¹Ne and ¹⁰Be/²¹Ne systematics in 16 DaG meteorites, we derived more reliable estimates of the ¹⁰Be/²¹Ne production rate ratio, which seems more sensitive to shielding than was predicted by the semi‐empirical model of Graf et al. (1990) but less sensitive than was predicted by the purely physical model of Leya et al. (2000).     

Chemical studies of H chondrites-10: Contents of thermally labile trace elements are unaffected by late heating

Abstract— We have used radiochemical neutron activation analysis (RNAA) to determine 15 trace elements, including 10 moderately to highly volatile ones—Rb, Ag, Se, Cs, Te, Zn, Cd, Bi, Tl, In (in increasing volatility order), in 6 H chondrite falls with low-³He contents. These (plus prior RNAA data) provide a compositional database of 92 H4-6 chondrite falls. Three suites of samples can be identified from their noble gas contents: 44 with “normal” contents and, therefore, “normal” orbits and cosmic-ray exposure histories; 8 that lost radiogenic gases, presumably by shock late in their histories; and 17 that lost cosmogenic gases by heating during close solar approach. We used the standard multivariate statistical techniques of linear discriminant analysis and logistic regression to compare contents of the 10 moderately and highly volatile trace elements, listed above, in these three suites. We found no significant differences. This contrasts sharply with similar comparisons involving random falls and H4-6 chondrites that landed on Earth at specific time intervals. Apparently, contents of volatile trace elements in H4-6 chondrites were established early in their histories, and they are so retentively sited that loss during later heating episodes did not occur.