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 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.     

The evolution of enstatite and chondrules in unequilibrated enstatite chondrites: Evidence from iron-rich pyroxene

Abstract— FeO-rich (Fs^6–34) pyroxene lacking cathodoluminescence (CL), hereafter black pyroxene, is a major constituent of some of the chondrules and fragments in unequilibrated (type 3) enstatite chondrites (UECs). It contains structurally oriented zones of Cr-, Mn-, V-rich, FeO-poor enstatite with red CL, associated with mm-sized blebs of low-Ni, Fe-metal and, in some cases, silica. These occurrences represent clear evidence of pyroxene reduction. The black pyroxene is nearly always rimmed by minor element (Cr, Mn, V)-poor enstatite having a blue CL. More commonly, red and blue enstatites, unassociated with black pyroxene, occur as larger grains in chondrules and fragments, and these constitute the major silicate phases in UECs. The REE abundance patterns of the black pyroxene are LREE-depleted. The blue enstatite rims, however, have a near-flat to LREE-enriched pattern, ～0.5–4x chondritic. The petrologic and trace element data indicate that the black pyroxene is from an earlier generation of chondrules that formed in a nebular region that was more oxidizing than that of the enstatite chondrites. Following solidification, these chondrules experienced a more reducing nebular environment and underwent reduction. Some, perhaps most, of the red enstatite that is common throughout the UECs may be the product of solid-state reduction of black pyroxene. The blue enstatite rims grew onto the surfaces of the black pyroxene and red enstatite as a result of condensation from a nebular gas. The evolutionary history of some of the enstatite and chondrules in enstatite chondrites can be expressed in a four-stage model that includes: Stage 1. Formation of chondrules in an oxidizing nebular environment Stage 2. Solid-state reduction of the more oxidized chondrules and fragments to red enstatite in a more reducing nebular environment Stage 3. Formation of blue enstatite rims on the black pyroxene as well as on the red enstatite. Stage 4. Reprocessing, by various degrees of melting, of many of the earlier-formed materials.     

Comparison of cosmic‐ray exposure ages and trapped noble gases in chondrule and matrix samples of ordinary,enstatite, and carbonaceous chondrites

Abstract— We performed a comprehensive study of the He, Ne, and Ar isotopic abundances and of the chemical composition of bulk material and components of the H chondrites Dhajala, Bath, Cullison, Grove Mountains 98004, Nadiabondi, Ogi, and Zag, of the L chondrites Grassland, Northwest Africa 055, Pavlograd, and Ladder Creek, of the E chondrite Indarch, and of the C chondrites Hammadah al Hamra 288, Acfer 059, and Allende. We discuss a procedure and necessary assumptions for the partitioning of measured data into cosmogenic, radiogenic, implanted, and indigenous noble gas components. For stone meteorites, we derive a cosmogenic ratio ²⁰Ne/²²Ne of 0.80 ± 0.03 and a trapped solar ⁴He/³He ratio of 3310 ± 130 using our own and literature data. Chondrules and matrix from nine meteorites were analyzed. Data from Dhajala chondrules suggest that some of these may have experienced precompaction irradiation by cosmic rays. The other chondrules and matrix samples yield consistent cosmic‐ray exposure (CRE) ages within experimental errors. Some CRE ages of some of the investigated meteorites fall into clusters typically observed for the respective meteorite groups. Only Bath's CRE age falls on the 7 Ma double‐peak of H chondrites, while Ogi's fits the 22 Ma peak. The studied chondrules contain trapped ²⁰Ne and ³⁶Ar concentrations in the range of 10^?6–10^?9 cm³ STP/g. In most chondrules, trapped Ar is of type Q (ordinary chondritic Ar), which suggests that this component is indigenous to the chondrule precursor material. The history of the Cullison chondrite is special in several respects: large fractions of both CR‐produced ³He and of radiogenic ⁴He were lost during or after parent body breakup, in the latter case possibly by solar heating at small perihelion distances. Furthermore, one of the matrix samples contains constituents with a regolith history on the parent body before compaction. It also contains trapped Ne with a ²⁰Ne/²²Ne ratio of 15.5 ± 0.5, apparently fractionated solar Ne.     

Noble gases in ten Nullarbor chondrites: Exposure ages,terrestrial ages,and weathering effects

Abstract— We present concentration and isotopic composition of He, Ne, and Ar in ten chondrites from the Nullarbor region in Western Australia as well as the concentrations of ⁸⁴Ke, ¹²⁹Xe, and ¹³²Xe. From the measured cosmogenic ¹⁴C concentrations (Jull et al. 1995), shielding‐corrected production rates of ¹⁴C are deduced using cosmogenic ²²Ne/²¹Ne ratios. For shielding conditions characterized by ²²Ne/²¹Ne >1.10, this correction becomes significant and results in shorter terrestrial ages. The exposure ages of the ten Nullarbor chondrites are in the range of values usually observed in ordinary chondrites. Some of the meteorites have lost radiogenic gases as well as cosmogenic ³He. Most of the analyzed specimens show additional trapped Ar, Kr, and Xe of terrestrial origin. The incorporation of these gases into weathering products is common in chondrites from hot deserts.     

Noble gas studies in CAIs from CV3 chondrites: No evidence for primordial noble gases

Abstract— Calcium‐aluminum‐rich inclusions (CAIs) were among the first solids in the solar system and were, similar to chondrules, created at very high temperatures. While in chondrules, trapped noble gases have recently been detected, the presence of trapped gases in CAIs is unclear but could have important implications for CAI formation and for early solar system evolution in general. To reassess this question, He, Ne, and Ar isotopes were measured in small, carefully separated and, thus, uncontaminated samples of CAIs from the CV3 chondrites Allende, Axtell, and Efremovka. The ²⁰Ne/²²Ne ratios of all CAIs studied here are <0.9, indicating the absence of trapped Ne as, e.g., Ne‐HL, Ne‐Q, or solar wind Ne. The ²¹Ne/²²Ne ratios range from 0.86 to 0.72, with fine‐grained, more altered CAIs usually showing lower values than coarse‐grained, less altered CAIs. This is attributed to variable amounts of cosmogenic Ne produced from Na‐rich alteration phases rather than to the presence of Ne‐G or Ne‐R (essentially pure ²²Ne) in the samples. Our interpretation is supported by model calculations of the isotopic composition of cosmogenic Ne in minerals common in CAIs. The ³⁶Ar/³⁸Ar ratios are between 0.7 and 4.8, with fine‐grained CAIs within one meteorite showing higher ratios than the coarse‐grained ones. This agrees with higher concentrations of cosmogenic ³⁶Ar produced by neutron capture on ³⁵Cl with subsequent β^?‐decay in finer‐grained, more altered, and thus, more Cl‐rich CAIs than in coarser‐grained, less altered ones. Although our data do not strictly contradict the presence of small amounts of Ne‐G, Ne‐R, or trapped Ar in the CAIs, our noble gas signatures are most simply explained by cosmogenic production, mainly from Na‐, Ca‐, and Cl‐rich minerals.     

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

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

The thermometry of enstatite chondrites: A brief review and update

Abstract— Due to the discoveries in Antarctica, the number of known enstatite chondrites has doubled in the last few years, and many rare or previously unknown types have been collected, most notably many EL3 and EH3 chondrites. We have applied the five major enstatite chondrite thermometers to the new and previously known enstatite chondrites, the thermometers being: (1) kamacite-quartz-enstatite-oldhamite-troilite (KQEOT), (2) oldhamite, (3) alabandite-niningerite, (4) sphalerite, and (5) phosphide-metal. Measured temperatures based on the KQEOT and oldhamite systems are 800 °C-1000 °C with the type 3 enstatite chondrites having values similar to those of type 4–6. It seems likely that these temperatures relate to events prior to parent body metamorphism, such as nebula condensation or chondrule formation, and were not significantly reset by later events. Measured temperatures for alabandite-niningerite, metal-phosphide and sphalerite in EH chondrites increase from 300 °C-400 °C to 600 °C-800 °C with petrographic indications of increasing metamorphism. In contrast, measured temperatures for all EL chondrites, including the most heavily metamorphosed, are generally <400 °C. Apparently EL chondrites cooled more slowly than the EH chondrites regardless of metamorphism experienced. Measured temperatures for the alabandite-niningerite, metal-phosphide and sphalerite are actually closure temperatures for the last thermal event suffered by the meteorite, and the fast cooling rates indicated are most consistent with processes occurring in thick regoliths.     

Manganese-chromium systematics in sulfides of unequilibrated enstatite chondrites

Abstract— We measured with a secondary ion mass spectrometer Mn/Cr ratios and Cr isotopes in individual grains of Mn-bearing sulfides (i.e., sphalerites, ZnS; alabandites, MnS; and niningerites, MgS) in nine unequilibrated enstatite chondrites (UECs). The goals were to determine whether live ⁵³Mn (half-life ～3.7 Ma) was incorporated in these objects at the time of their isotopic closure and to establish whether Mn-Cr systematics in sulfides in UECs can be used as a high-resolution chronometer to constrain formation time differences between these meteorites. Sulfide grains analysed in four of these UECs, MAC 88136 (EL3), MAC 88184 (EL3), MAC 88180 (EL3), and Indarch (EH4), have clear ⁵³Cr excesses. These ⁵³Cr excesses can be very large (δ⁵³Cr/⁵²Cr ranges up to ～18,400%, the largest ⁵³Cr excess measured so far) and, in some grains, are well correlated with the Mn/Cr ratios. Thus, they were most likely produced by the in situ decay of ⁵³Mn in the meteorite samples. In the remaining five meteorites, no detectable excesses of ⁵³Cr were found, and only upper limits on the initial ⁵³Mn/⁵⁵Mn ratios could be established. The four meteorites with ⁵³Cr excesses show variations in the inferred ⁵³Mn/⁵⁵Mn ratios in various sulfide grains of the same meteorite. The Mn-Cr systematics in these sulfides were disturbed (during and/or after the decay of ⁵³Mn) by varying degrees of reequilibration. Provided ⁵³Mn was homogeneously distributed in the region of the early solar system where these objects formed, the data suggest that the time of the last isotopic equilibration of sulfides in EL chondrites occurred at least 3 Ma after a similar episode in EH 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.     

Occurrence and implications of silicon nitride in enstatite chondrites

Abstract— Silicon nitride, Si₃N₄, has previously been observed to be a common constituent of acid residues of Qingzhen (EH3) and Indarch (EH4). Ion probe analysis of the Si, N and C isotopic compositions of individual Si₃N₄ grains from Qingzhen and Indarch acid residues suggest most, if not all, grains are Solar System in origin. A few grains have isotopically anomalous C but this is probably due to small presolar SiC grains adhering to them. In situ observations of the Si₃N₄ in Qingzhen show that it is only present within, and probably exsolved from, host phases which contain elemental Si in solid solution. Thermodynamic calculations suggest that the Si₃N₄ probably formed during metamorphism and not in the nebula. Thermodynamic calculations also show that sinoite (Si₂N₂O) and not Si₃N₄ should be the stable phase during metamorphism. It appears that kinetic factors must have inhibited the formation of sinoite in Qingzhen and Indarch.     

Calcium‐aluminum‐rich inclusions in enstatite chondrites (II): Oxygen isotopes

Abstract— In situ io n microprobe analyses of spinel in refractory calcium‐aluminium‐rich inclusions (CAIs) from type 3 EH chondrites yield ¹⁶O‐rich compositions (δ ¹⁸O and δ ¹⁷O about‐40‰). Spinel and feldspar in a CAI from an EL3 chondrite have significantly heavier isotopic compositions (δ ¹⁸O and δ ¹⁷O about ?5‰). A regression through the data results in a line with slope 1.0 on a three‐isotope plot, similar to isotopic results from unaltered minerals in CAIs from carbonaceous chondrites. The existence of CAIs with ¹⁶O‐rich and ¹⁶O‐poor compositions in carbonaceous as well as enstatite chondrites indicates that CAIs formed in at least two temporally or spatially distinct oxygen reservoirs. General similarities in oxygen isotopic compositions of CAIs from enstatite, carbonaceous, and ordinary chondrites indicate a common nebular mechanism or locale for the production of most CAIs.     

A condensation model for the formation of chondrules in enstatite chondrites

Abstract— It is proposed that the chondrules in enstatite chondrites formed near the Sun from rain‐like supercooled liquid silicate droplets and condensed Fe‐Ni alloys in thermodynamic equilibrium with a slowly cooling nebula. FeO formed and dissolved in the droplets in an initial stage when the nucleation of iron was blocked, and was later mostly reduced to unalloyed Fe. At high temperatures, the silicate droplets contained high concentrations of the less volatile components CaO and Al₂O₃. At somewhat lower temperatures the equilibrium MgO content of the droplets was relatively high. As cooling progressed, some droplets gravitated toward the Sun, and moved in other directions, depleting the region in CaO, Al₂O₃, and MgO and accounting for the relatively low observed CaO/SiO₂, Al₂O₃/SiO₂, and MgO/SiO₂ ratios in enstatite chondrites. At approximately 1400 K, the remaining supercooled silicate droplets crystallized to form MgSiO₃ (enstatite) with small amounts of olivine and a high‐SiO₂ liquid phase which became the mesostases. The high enstatite content is the result of the supercooled chondrules crystallizing at a relatively low temperature and relatively high total pressure. Finally, FeS formed at temperatures below 680 K by reaction of the condensed Fe with H₂S. All calculations were performed with the evaluated optimized thermodynamic databases of the FactSage thermodynamic computer system. The thermodynamic properties of compounds and solutions in these databases were optimized completely independently of any meteoritic data. Agreement of the model with observed bulk and phase compositions of enstatite chondrules is very good and is generally within experimental error limits for all components and phases.     

The trapped noble gas component in achondrites

Abstract— The trapped noble gases Ar, Kr and Xe in several achondrites were analysed. We chose separates of the lodranites Lodran and Graves Nunataks 95209 and bulk samples of the Tatahouine diogenite, Pasamonte eucrite, five aubrites and two angrites. Among these, Lodran, Tatahouine, Pasamonte and the aubrite Norton County have been reported to contain U‐Xe, a noble gas component assumed to be the most primitive component in the solar system. U‐Xe might have been incorporated into the early Earth. We found large concentrations of Xe in several separates of the Lodran lodranite, however, none of the measurements revealed U‐Xe composition. The Xe composition of all achondrites can straightforwardly be explained with mixtures of trapped common Xe‐Q, absorbed air and various amounts of fissiogenic and cosmogenic Xe. Reanalysis of literature data for Pasamonte, Angra dos Reis and some aubrites is consistent with Xe‐Q as the trapped endmember component and contributions of fissiogenic Xe. The presence of Xe‐Q in many primitive achondrites is in agreement with the formation of their parent bodies from originally chondritic precursor material. The Ar‐Xe elemental composition of Lodran and the aubrites indicate subsolar composition, which is commonly found in E chondrites. This result supports a model of formation of the aubrites from E‐chondritic precursor material.     

On the significance of diopside and oldhamite in enstatite chondrites and aubrites

Abstract— Enstatite is the primary silicate phase of equilibrated enstatite chondrites (EECs). The CaO contents of these enstatites lie close to or on the enstatite-diopside phase boundary, yet, curiously, diopside has always been absent from EEC assemblages. In contrast, aubrites contain abundant diopside even though they are thought to be derived from an E chondrite-like protolith. A phase equilibrium analysis of the Ca-Mg-Fe-Mn-Si-O-S system under reducing conditions solves this enigma and shows that diopside-bearing EECs should commonly be found. When S fugacity is sufficiently high (e.g., Fe-FeS buffer), low O fugacity limits the stability of diopside in favor of oldhamite. Under such conditions, the relative stability of diopside and oldhamite is described by the reaction: CaMgSi₂O₆ + MgS = CaS + Mg₂Si₂O₆ A large bulk compositional field exists where diopside and oldhamite are simultaneously stable. The existence of oldhamite does not preclude the stability of diopside. Phase diagram topology demonstrates that bulk compositions lying in the enstatite-oldhamite field and enstatite-oldhamite-alabandite field have enstatite CaO contents nearly identical to that of enstatite in equilibrium with diopside alone. This explains the high enstatite CaO contents of all EECs that do not contain diopside. This study also reports the discovery of the first EEC to contain metamorphic diopside, the Antarctic meteorite EET 90102. Elephant Moraine 90102 has a typical EL6 texture and contains the assemblage: enstatite, diopside, albite, kamacite, troilite, sinoite, and graphite. Trace quantities of alabandite, oldhamite and daubreelite are also present. Diopside is stable in EET 90102 because its bulk composition lies within either the enstatite-diopside-oldhamite-alabandite or diopside-alabandite-enstatite stability fields. In contrast, all other EECs analyzed to date have bulk compositions lying in the enstatite-oldhamite-alabandite stability field. The discovery of diopside in EET 90102 helps confirm the predictions of the phase equilibrium analysis. Elephant Moraine 90102 experienced a high-temperature metamorphic equilibration from which it was quenched. The enstatite-diopside, CaS in alabandite and Fe in alabandite, geothermometers yield temperatures of last equilibration of ～900 °C. The absence of daubreelite and schreibersite along with high troilite Cr contents and high kamacite P contents confirm a high-temperature metamorphic quench. The EET 90102 chondrite experienced a somewhat different cooling history and has a slightly different bulk composition than all other EECs studied to date; however, the close mineralogic, petrologic and textural similarities between EET 90102 and nominal EL6 chondrites signify that it should be classified as a diopside- and sinoite-bearing EL6 chondrite. Assuming that the aubrites formed from an E chondrite-like protolith, a source rock similar to that of a diopside-bearing EEC offers a clear advantage for aubrite formation. Melting of a diopside-saturated EEC protolith would not require conversion of CaS to achieve diopside-saturation upon cooling.     

The isotopic composition and origins of silicon nitride from ordinary and enstatite chondrites

Abstract— The N-isotopic composition of acid-resistant residues of three low petrologic type ordinary chondrites (Adrar 003, LL3.2; Inman, L3.4; Tieschitz, H3.6) and an enstatite chondrite (Indarch, EH4) have been measured by static mass spectrometry. All of these samples have been shown by transmission electron microscopy (TEM) to contain silicon nitride (Si₃N₄), and no other nitrides were detected in any of the residues (Lee et al., 1995). Stepped combustion has demonstrated the presence of at least two components with low C/N ratios, which have been interpreted as Si₃N₄. The most abundant component, common to all the meteorites studied, released during combustion at temperatures >1150 °C, may have formed during metamorphism of the meteorite's parent body. In addition, the ordinary chondrites Tieschitz and Inman show evidence for a second component of Si₃N₄ that is less stable to combustion than the first and is enriched in ¹⁵N. The unusual N-isotope signature suggests that this second type of Si₃N₄ may constitute a new type of interstellar grain. A comparison of the isotope and microscope data suggests that the >1150 °C component can be related to nierite (α-Si₃N₄) and the less stable component to β-Si₃N₄.     

Plausible parent bodies for enstatite chondrites and mesosiderites: Implications for Lutetia's fly-by

We present new irradiation experiments performed on the enstatite chondrite Eagle (EL6) and the mesosiderite Vaca Muerta. These experiments were performed with the aims of (a) quantifying the spectral effect of the solar wind on their parent asteroid surfaces and (b) identifying their parent bodies within the asteroid belt. For Vaca Muerta we observe a reddening and darkening of the reflectance spectrum with progressive irradiation, consistent with what is observed in the cases of silicates and silicate-rich meteorites such as OCs and HEDs. For Eagle we observe little spectral variation, and therefore we do not expect to observe a significant spectral difference between EC meteorites and their parent bodies. We evaluated possible parent bodies for both meteorites by comparing their VNIR spectra (before and after irradiation) with those of ∼400 main-belt asteroids. We found that 21 Lutetia (Rosetta's forthcoming fly-by target) and 97 Klotho (both Xc types in the new Bus-DeMeo taxonomy) have physical properties compatible with those of enstatite chondrite meteorites while 201 Penelope, 250 Bettina and 337 Devosa (all three are Xk types in the Bus-DeMeo taxonomy) are compatible with the properties of mesosiderites.     

Hydrothermal alteration experiments of enstatite: Implications for aqueous alteration of carbonaceous chondrites

Abstract— Enstatite is one of the major constituent minerals in carbonaceous chondrites. Hydrothermal alteration experiments (26 in total) of enstatite were carried out at pH 0, 6, 7, 12, 13, and 14, at temperatures of 100, 200, and 300 °C, and for run durations of 24, 72, 168, and 336 h in order to provide constraints on the aqueous‐alteration conditions of the meteorites. The recovered samples were studied in detail by using powder X‐ray diffraction, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Under acidic and mildly acidic conditions (pH 0, 6), no significant alteration occurred, whereas under neutral to alkaline conditions (pH 7–14), serpentine and saponite formed in various proportions by replacing enstatite. At 300 °C for 168 h, serpentine formed under neutral to moderately alkaline conditions (pH 7, 12), and serpentine and saponite formed as unit cell‐scale coherent intergrowths under highly alkaline conditions (pH 13, 14). The amounts of phyllosilicates have a tendency to increase with increasing pH, temperature, and run duration. There is also a tendency for saponite to form at higher pH and temperature and under longer run‐durations than serpentine. The results indicate that alteration of enstatite is strongly dependent on the experimental conditions, especially pH. They suggest that CM chondrites experienced aqueous alteration under neutral to alkaline conditions, whereas CV and CI chondrites experienced aqueous alteration under more alkaline conditions. The results also suggest that aqueous alteration in CI chondrites occurred at higher temperatures than in CM chondrites, and aqueous alteration in CV chondrites occurred at even higher temperatures than in CI chondrites.     

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.