New measurement technique for characterizing small extraterrestrial materials by X‐ray diffraction using the Gandolfi attachment

Identification and characterization of small extraterrestrial samples, such as small Antarctic meteorites <~1 cm, require the development of convenient laboratory‐based nondestructive analytical techniques using X‐ray diffraction (XRD). We explore the characterization criteria using an X‐ray diffractometer with a Gandolfi attachment using sub‐mm small fragments and powder aggregates for various kinds of stony meteorites and develop a new analytical technique. We primarily focus on olivine and pyroxene because they are the most abundant and important minerals for stony meteorite classification. A new calibration is performed to estimate the FeO content of the olivine in unequilibrated ordinary chondrites, which is useful for determining the meteorite chemical group irrespective of powder aggregate diameter but dependent on fragment grain diameter. This is because X‐ray intensity absorption is more effective for grains than for powders. Clinoenstatite (Cen) and orthoenstatite (Oen) were distinguished using the presence or absence of the isolated Oen 511 index peak. The method is also applied to other stony meteorites including carbonaceous chondrites and achondrites. The XRD results are consistent with studies based on polished sections involving textural observations by scanning microscope and chemical compositions of the constituent minerals. The new measurement technique presented here is convenient because of its use in air by the laboratory‐based X‐ray diffractometer, which makes it useful for the initial analyses of restricted extraterrestrial sample characterization.     

A critical evaluation of oxidation versus reduction during metamorphism of L and LL group chondrites,and implications for asteroid spectroscopy

Abstract— Modal mineralogies of individual, equilibrated (petrologic type 4–6 L and LL chondrites have been measured using an electron microprobe mapping technique, and the chemical compositions of coexisting silicate minerals have been analyzed. Progressive changes in the relative abundances and in the molar Fe/Mn and Fe/Mg ratios of olivine, low‐Ca pyroxene, and diopside occur with increasing metamorphic grade. Variations in olivine/low‐Ca pyroxene ratios (Ol/Px) and in metal abundances and compositions with petrologic type support the hypothesis that oxidation of metallic iron accompanied thermal metamorphism in ordinary chondrites. Modal Ol/Px ratios are systematically lower than normative Ol/Px ratios for the same meteorites, suggesting that the commonly used C.I.P.W. norm calculation procedure may not adequately estimate silicate mineral abundances in reduced chondrites. Ol/Px ratios calculated from visible and near‐infrared (VISNIR) reflectance spectra of the same meteorites are not in agreement with other Ol/Px determinations, possibly because of spectral complexities arising from other minerals in chondrites. Characteristic features in VISNIR spectra are sensitive to the proportions and compositions of olivine and pyroxenes, the minerals most affected by oxidative metamorphism. This work may allow spectral calibration for the determination of mineralogy and petrologic type, and thus may be useful for spectroscopic studies of asteroids.     

Ordinary chondrite metallography: Part 2. Formation of zoned and unzoned metal particles in relatively unshocked H,L, and LL chondrites

Abstract— We studied the metallography of Fe‐Ni metal particles in 17 relatively unshocked ordinary chondrites and interpreted their microstructures using the results of P‐free, Fe‐Ni alloy cooling experiments (described in Reisener and Goldstein 2003). Two types of Fe‐Ni metal particles were observed in the chondrites: zoned taenite + kamacite particles and zoneless plessite particles, which lack systematic Ni zoning and consist of tetrataenite in a kamacite matrix. Both types of metal particles formed during metamorphism in a parent body from homogeneous, P‐poor taenite grains. The phase transformations during cooling from peak metamorphic temperatures were controlled by the presence or absence of grain boundaries in the taenite particles. Polycrystalline taenite particles transformed to zoned taenite + kamacite particles by kamacite nucleation at taenite/taenite grain boundaries during cooling. Monocrystalline taenite particles transformed to zoneless plessite particles by martensite formation and subsequent martensite decomposition to tetrataenite and kamacite during the same cooling process. The varying proportions of zoned taenite + kamacite particles and zoneless plessite particles in types 4–6 ordinary chondrites can be attributed to the conversion of polycrystalline taenite to monocrystalline taenite during metamorphism. Type 4 chondrites have no zoneless plessite particles because metamorphism was not intense enough to form monocrystalline taenite particles. Type 6 chondrites have larger and more abundant zoneless plessite particles than type 5 chondrites because intense metamorphism in type 6 chondrites generated more monocrystalline taenite particles. The distribution of zoneless plessite particles in ordinary chondrites is entirely consistent with our understanding of Fe‐Ni alloy phase transformations during cooling. The distribution cannot be explained by hot accretion‐autometamorphism, post‐metamorphic brecciation, or shock processing.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

Fe‐Ni metal in primitive chondrites: Indicators of classification and metamorphic conditions for ordinary and CO chondrites

Abstract— We report the results of our petrological and mineralogical study of Fe‐Ni metal in type 3 ordinary and CO chondrites, and the ungrouped carbonaceous chondrite Acfer 094. Fe‐Ni metal in ordinary and CO chondrites occurs in chondrule interiors, on chondrule surfaces, and as isolated grains in the matrix. Isolated Ni‐rich metal in chondrites of petrologic type lower than type 3.10 is enriched in Co relative to the kamacite in chondrules. However, Ni‐rich metal in type 3.15–3.9 chondrites always contains less Co than does kamacite. Fe‐Ni metal grains in chondrules in Semarkona typically show plessitic intergrowths consisting of submicrometer kamacite and Ni‐rich regions. Metal in other type 3 chondrites is composed of fine‐ to coarse‐grained aggregates of kamacite and Ni‐rich metal, resulting from metamorphism in the parent body. We found that the number density of Ni‐rich grains in metal (number of Ni‐rich grains per unit area of metal) in chondrules systematically decreases with increasing petrologic type. Thus, Fe‐Ni metal is a highly sensitive recorder of metamorphism in ordinary and carbonaceous chondrites, and can be used to distinguish petrologic type and identify the least thermally metamorphosed chondrites. Among the known ordinary and CO chondrites, Semarkona is the most primitive. The range of metamorphic temperatures were similar for type 3 ordinary and CO chondrites, despite them having different parent bodies. Most Fe‐Ni metal in Acfer 094 is martensite, and it preserves primary features. The degree of metamorphism is lower in Acfer 094, a true type 3.00 chondrite, than in Semarkona, which should be reclassified as type 3.01.     

Intermineral oxygen three‐isotope systematics of silicate minerals in equilibrated ordinary chondrites

High‐precision oxygen three‐isotope ratios were measured for four mineral phases (olivine, low‐Ca and high‐Ca pyroxene, and plagioclase) in equilibrated ordinary chondrites (EOCs) using a secondary ion mass spectrometer. Eleven EOCs were studied that cover all groups (H, L, LL) and petrologic types (4, 5, 6), including S1–S4 shock stages, as well as unbrecciated and brecciated meteorites. SIMS analyses of multiple minerals were made in close proximity (mostly <100 μm) from several areas in each meteorite thin section, to evaluate isotope exchange among minerals. Oxygen isotope ratios in each mineral become more homogenized as petrologic type increases with the notable exception of brecciated samples. In type 4 chondrites, oxygen isotope ratios of olivine and low‐Ca pyroxene are heterogeneous in both δ¹⁸O and Δ¹⁷O, showing similar systematics to those in type 3 chondrites. In type 5 and 6 chondrites, oxygen isotope ratios of the four mineral phases plot along mass‐dependent fractionation lines that are consistent with the bulk average Δ¹⁷O of each chondrite group. The δ¹⁸O of three minerals, low‐Ca and high‐Ca pyroxene and plagioclase, are consistent with equilibrium fractionation at temperatures of 700–1000 °C. In most cases the δ¹⁸O values of olivine are higher than those expected from pyroxene and plagioclase, suggesting partial retention of premetamorphic values due to slower oxygen isotope diffusion in olivine than pyroxene during thermal metamorphism in ordinary chondrite parent bodies.     

Hydrogen and major element concentrations on 433 Eros: Evidence for an L‐ or LL‐chondrite‐like surface composition

A reanalysis of NEAR X‐ray/gamma‐ray spectrometer (XGRS) data provides robust evidence that the elemental composition of the near‐Earth asteroid 433 Eros is consistent with the L and LL ordinary chondrites. These results facilitated the use of the gamma‐ray measurements to produce the first in situ measurement of hydrogen concentrations on an asteroid. The measured value,  ppm, is consistent with hydrogen concentrations measured in L and LL chondrite meteorite falls. Gamma‐ray derived abundances of hydrogen and potassium show no evidence for depletion of volatiles relative to ordinary chondrites, suggesting that the sulfur depletion observed in X‐ray data is a surficial effect, consistent with a space‐weathering origin. The newfound agreement between the X‐ray, gamma‐ray, and spectral data suggests that the NEAR landing site, a ponded regolith deposit, has an elemental composition that is indistinguishable from the mean surface. This observation argues against a pond formation process that segregates metals from silicates, and instead suggests that the differences observed in reflectance spectra between the ponds and bulk Eros are due to grain size differences resulting from granular sorting of ponded material.     

Metal phases in ordinary chondrites: Magnetic hysteresis properties and implications for thermal history

Magnetic properties are sensitive proxies to characterize FeNi metal phases in meteorites. We present a data set of magnetic hysteresis properties of 91 ordinary chondrite falls. We show that hysteresis properties are distinctive of individual meteorites while homogeneous among meteorite subsamples. Except for the most primitive chondrites, these properties can be explained by a mixture of multidomain kamacite that dominates the induced magnetism and tetrataenite (both in the cloudy zone as single‐domain grains, and as larger multidomain grains in plessite and in the rim of zoned taenite) dominates the remanent magnetism, in agreement with previous microscopic magnetic observations. The bulk metal contents derived from magnetic measurements are in agreement with those estimated previously from chemical analyses. We evidence a decreasing metal content with increasing petrologic type in ordinary chondrites, compatible with oxidation of metal during thermal metamorphism. Types 5 and 6 ordinary chondrites have higher tetrataenite content than type 4 chondrites. This is compatible with lower cooling rates in the 650–450 °C interval for higher petrographic types (consistent with an onion‐shell model), but is more likely the result of the oxidation of ordinary chondrites with increasing metamorphism. In equilibrated chondrites, shock‐related transient heating events above approximately 500 °C result in the disordering of tetrataenite and associated drastic change in magnetic properties. As a good indicator of the amount of tetrataenite, hysteresis properties are a very sensitive proxy of the thermal history of ordinary chondrites, revealing low cooling rates during thermal metamorphism and high cooling rates (e.g., following shock reheating or excavation after thermal metamorphism). Our data strengthen the view that the poor magnetic recording properties of multidomain kamacite and the secondary origin of tetrataenite make equilibrated ordinary chondrites challenging targets for paleomagnetic study.     

Determination of the equilibrium fO2 in bulk samples of H,L, and LL ordinary chondrites by solid‐state electrochemistry

High‐temperature solid‐state electrochemistry techniques (EMF method) were used to measure the oxygen fugacity (fO₂) of the ordinary chondrites Ochansk (H4), Savtschenskoje (LL4), Elenovka (L5), Vengerovo (H5), and Kharkov (L6). The fO₂ results are presented in the form of the following equations: It was found that fO₂ regularly increases from H chondrites to LL chondrites. Measured fO₂ are ~1.5 higher than those previously calculated from mineral assemblages. Kharkov (L6) is a little more oxidized than Elenovka (L5) in agreement with the progressive oxidation model. At the same time, Ochansk (H4) is more oxidized than Vengerovo (H5) and exhibits a slightly different slope compared to other chondrites and at T > 1200 K, becomes more reduced than Kharkov (L6) or Elenovka (L5). Measured oxygen fugacity values of meteorites fall within (0.1–1.0)·log fO₂ of one another. The possible explanation of discrepancies between measured and calculated values is discussed.     

In situ analysis of platinum group elements in equilibrated ordinary chondrite kamacite and taenite

Platinum group element (PGE) concentrations have been determined in situ in ordinary chondrite kamacite and taenite grains via laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS). Results demonstrate that PGE concentrations in ordinary chondrite metal (kamacite and taenite) are similar among the three ordinary chondrite groups, in contrast to previous bulk metal studies in which PGE concentrations vary in the order H < L < LL. PGE concentrations are higher in taenite than kamacite, consistent with preferential PGE partitioning into taenite. PGE concentrations vary between and within metal grains, although average concentrations in kamacite broadly agree with results from bulk studies. The variability of PGE concentrations in metal decreases with increasing petrologic type; however, variability is still evident in most type six ordinary chondrites, suggesting that equilibration of PGEs does not occur between metal grains, but rather within individual metal grains via self‐diffusion during metamorphism. The constant average PGE concentrations within metal grains across different ordinary chondrite groups are consistent with the formation of metal via nebular condensation prior to the accretion of ordinary chondrite parent bodies. Post‐condensation effects, including heating during chondrule‐formation events, may have affected some element ratios, but have not significantly affected average metal PGE concentrations.     

The formation of Ca‐, Fe‐rich silicates in reduced and oxidized CV chondrites: The roles of impact‐modified porosity and permeability,and heterogeneous distribution of water ices

CV (Vigarano type) carbonaceous chondrites, comprising Allende‐like (CV_oxA) and Bali‐like (CV_oxB) oxidized and reduced (CV_red) subgroups, experienced differing degrees of fluid‐assisted thermal and shock metamorphism. The abundance and speciation of secondary minerals produced during asteroidal alteration differ among the subgroups: (1) ferroan olivine and diopside–hedenbergite solid solution pyroxenes are common in all CVs; (2) nepheline and sodalite are abundant in CV_oxA, rare in CV_red, and absent in CV_oxB; (3) phyllosilicates and nearly pure fayalite are common in CV_oxB, rare in CV_red, and virtually absent in CV_oxA; (4) andradite, magnetite, and Fe‐Ni‐sulfides are common in oxidized CVs, but rare in reduced CVs; the latter contain kirschsteinite instead. Thus, a previously unrecognized correlation exists between meteorite bulk permeabilities and porosities with the speciation of the Ca‐, Fe‐rich silicates (pyroxenes, andradite, kirschsteinite) among the CVox and CVred meteorites. The extent of secondary mineralization was controlled by the distribution of water ices, permeability, and porosity, which in turn were controlled by impacts on the asteroidal parent body. More intense shock metamorphism in the region where the reduced CVs originated decreased their porosity and permeability while simultaneously expelling intergranular ices and fluids. The mineralogy, petrography, and bulk chemical compositions of both the reduced and oxidized CV chondrites indicate that mobile elements were redistributed between Ca,Al‐rich inclusions, dark inclusions, chondrules, and matrices only locally; there is no evidence for large‐scale (>several cm) fluid transport. Published ⁵³Mn‐⁵³Cr ages of secondary fayalite in CV, CO, and unequilibrated ordinary chondrites, and carbonates in CI, CM, and CR chondrites are consistent with aqueous alteration initiated by heating of water ice‐bearing asteroids by decay of ²⁶Al, not shock metamorphism.     

Shock stage distribution of 2280 ordinary chondrites—Can bulk chondrites with a shock stage of S6 exist as individual rocks?

The brecciation and shock classification of 2280 ordinary chondrites of the meteorite thin section collection at the Institut für Planetologie (Münster) has been determined. The shock degree of S3 is the most abundant shock stage for the H and LL chondrites (44% and 41%, respectively), while the L chondrites are on average more heavily shocked having more than 40% of rocks of shock stage S4. Among the H and LL chondrites, 40–50% are “unshocked” or “very weakly shocked.” Considering the petrologic types, in general, the shock degree is increasing with petrologic type. This is the case for all meteorite groups. The main criteria to define a rock as an S6 chondrite are the solid‐state recrystallization and staining of olivine and the melting of plagioclase often accompanied by the formation of high‐pressure phases like ringwoodite. These characteristics are typically restricted to local regions of a bulk chondrite in or near melt zones. In the past, the identification of high‐pressure minerals (e.g., ringwoodite) was often taken as an automatic and practical criterion for a S6 classification during chondrite bulk rock studies. The shock stage classification of many significantly shocked chondrites (>S3) revealed that most ringwoodite‐bearing rocks still contain more than 25% plagioclase (74%). Thus, these bulk chondrites do not even fulfill the S5 criterion (e.g., 75% of plagioclase has to be transformed into maskelynite) and have to be classified as S4. Studying chondrites on typically large thin sections (several cm²) and/or using samples from different areas of the meteorites, bulk chondrites of shock stage S6 should be extremely rare. In this respect, the paper will discuss the probability of the existence of bulk rocks of S6.     

The Vicência meteorite fall: A new unshocked (S1) weakly metamorphosed (3.2) LL chondrite

The Vicência meteorite, a stone of 1.547 kg, fell on September 21, 2013, at the village Borracha, near the city of Vicência, Pernambuco, Brazil. It was recovered immediately after the fall, and our consortium study showed it to be an unshocked (S1) LL3.2 ordinary chondrite. The LL group classification is based on the bulk density (3.13 g cm^?3); the chondrule mean apparent diameter (0.9 mm); the bulk oxygen isotopic composition (δ¹⁷O = 3.768 ± 0.042‰, δ¹⁸O = 5.359 ± 0.042‰, Δ¹⁷O = 0.981 ± 0.020‰); the content of metallic Fe,Ni (1.8 vol%); the Co content of kamacite (1.73 wt%); the bulk contents of the siderophile elements Ir and Co versus Au; and the ratios of metallic Fe⁰/total iron (0.105) versus total Fe/Mg (1.164), and of Ni/Mg (0.057) versus total Fe/Mg. The petrologic type 3.2 classification is indicated by the beautifully developed chondritic texture, the standard deviation (~0.09) versus mean Cr₂O₃ content (~0.14 wt%) of ferroan olivine, the TL sensitivity and the peak temperature and peak width at half maximum, the cathodoluminescence properties of chondrules, the content of trapped ¹³²Xe_tr (0.317 × 10^?8cm³STP g^?1), and the Raman spectra for organic material in the matrix. The cosmic ray exposure age is ~72 Ma, which is at the upper end of the age distribution of LL group chondrites. The meteorite is unusual in that it contains relatively large, up to nearly 100 μm in size, secondary fayalite grains, defined as olivine with Fa_>75, large enough to allow in situ measurement of oxygen and Mn‐Cr isotope systematics with SIMS. Its oxygen isotopes plot along a mass‐dependent fractionation line with a slope of ~0.5 and Δ¹⁷O of 4.0 ± 0.3‰, and are similar to those of secondary fayalite and magnetite in the unequilibrated chondrites EET 90161, MET 96503, and Ngawi. These data suggest that secondary fayalite in Vicência was in equilibrium with a fluid with a Δ¹⁷O of ~4‰, consistent with the composition of the fluid in equilibrium with secondary magnetite and fayalite in other unequilibrated ordinary chondrites. Secondary fayalite and the chondrule olivine phenocrysts in Vicência are not in isotopic equilibrium, consistent with low‐temperature formation of fayalite during aqueous alteration on the LL parent body. That alteration, as dated by the ⁵³Mn‐⁵³Cr chronology age of secondary fayalite, took place $4.0{}_{?1.1}^{+1.4}$ Ma after formation of CV CAIs when anchored to the quenched angrite D'Orbigny.     

Systematics of Mössbauer absorption areas in ordinary chondrites and applications to a newly fallen meteorite in Jodhpur,India

Abstract— Mössbauer absorption areas corresponding to ⁵⁷Fe in olivine, pyroxene, troilite, and the metallic phase in ordinary chondrites are shown to exhibit certain systematic behaviors. H chondrites occupy 2 distinct regions on the plot of metallic phase absorption area versus silicate absorption area, while L/LL chondrites fall in a separate region. Similar separation is also observed when pyroxene absorption area is plotted against olivine absorption area. The one‐dimensional plot for the ratio of olivine area to pyroxene area separates L and LL chondrites. Based on these systematics, a newly fallen meteorite at Jodhpur, India is suggested to be an LL chondrite.     

Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies

In ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent‐body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4–6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all three OC groups. Apatite in L chondrites is Cl‐rich, similar to H chondrites, whereas apatite in LL chondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend to LL chondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4–6. Alkali‐ and halogen‐rich and likely hydrous metasomatic fluids acted during prograde metamorphism on OC parent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl‐rich composition after the asteroid began to cool. Differences in secondary minerals between H and L, LL chondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology‐dependent apatite compositions. Bulk Cl/F ratios for OCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios in OCs are similar to CI.     

Minor and trace element concentrations in adjacent kamacite and taenite in the Krymka chondrite

We report in situ NanoSIMS siderophile minor and trace element abundances in individual Fe‐Ni metal grains in the unequilibrated chondrite Krymka (LL3.2). Associated kamacite and taenite of 10 metal grains in four chondrules and one matrix metal were analyzed for elemental concentrations of Fe, Ni, Co, Cu, Rh, Ir, and Pt. The results show large elemental variations among the metal grains. However, complementary and correlative variations exist between adjacent kamacite‐taenite. This is consistent with the unequilibrated character of the chondrite and corroborates an attainment of chemical equilibrium between the metal phases. The calculated equilibrium temperature is 446 ± 9 °C. This is concordant with the range given by Kimura et al. (2008) for the Krymka postaccretion thermal metamorphism. Based on Ni diffusivity in taenite, a slow cooling rate is estimated of the Krymka parent body that does not exceed ~1K Myr^?1, which is consistent with cooling rates inferred by other workers for unequilibrated ordinary chondrites. Elemental ionic radii might have played a role in controlling elemental partitioning between kamacite and taenite. The bulk compositions of the Krymka metal grains have nonsolar (mostly subsolar) element/Ni ratios suggesting the Fe‐Ni grains could have formed from distinct precursors of nonsolar compositions or had their compositions modified subsequent to chondrule formation events.     

A comparison of FeO-rich,porphyritic olivine chondrules in unequilibrated chondrites and experimental analogues

Abstract Experimentally produced analogues of porphyritic olivine (PO) chondrules in ordinary chondrites provide an important insight into chondrule formation processes. We have studied experimental samples with PO textures grown at three different cooling rates (2, 5 and 100 *C/h), and samples that have been annealed at high temperatures (1000–1200 °C) subsequent to cooling. These are compared with natural chondrules of similar composition and texture from the ordinary chondrites Semarkona (LL3.0) and ALH 81251 (LL3.3). Zoning properties of olivine grains indicate that the Semarkona chondrules cooled at comparable rates to the experiments. Zoning in olivine from chondrules in ALH 81251 is not consistent with cooling alone but indicates that the chondrules underwent an annealing process. Chromium loss from olivine is very rapid during annealing and calculated diffusion coefficients for Cr in olivine are very similar to those of Fe-Mg interdiffusion coefficients under the same conditions. Annealed experimental samples contain an aluminous, low-Ca pyroxene which forms by reaction of olivine and liquid. No similar reaction texture is observed in ALH 81251 chondrules, and this may be evidence that annealing of the natural samples took place at considerably lower temperatures than the experimental analogues. The study supports the model of chondrule formation in a cool nebula and metamorphism of partly equilibrated chondrites during reheating episodes on the chondrite parent bodies.     

Size‐frequency distributions of chondrules and chondrule fragments in LL3 chondrites: Implications for parent‐body fragmentation of chondrules

Abstract— We measured the sizes and textural types of 719 intact chondrules and 1322 chondrule fragments in thin sections of Semarkona (LL3.0), Bishunpur (LL3.1), Krymka (LL3.1), Piancaldoli (LL3.4) and Lewis Cliff 88175 (LL3.8). The mean apparent diameter of chondrules in these LL3 chondrites is 0.80 φ units or 570 μm, much smaller than the previous rough estimate of ～900 μm. Chondrule fragments in the five LL3 chondrites have a mean apparent cross‐section of 1.60 φ units or 330 μm. The smallest fragments are isolated olivine and pyroxene grains; these are probably phenocrysts liberated from disrupted porphyritic chondrules. All five LL3 chondrites have fragment/ chondrule number ratios exceeding unity, suggesting that substantial numbers of the chondrules in these rocks were shattered. Most fragmentation probably occurred on the parent asteroid. Porphyritic chondrules (porphyritic olivine + porphyritic pyroxene + porphyritic olivine‐pyroxene) are more readily broken than droplet chondrules (barred olivine + radial pyroxene + cryptocrystalline). The porphyritic fragment/chondrule number ratio (2.0) appreciably exceeds that of droplet‐textured objects (0.9). Intact droplet chondrules have a larger mean size than intact porphyritic chondrules, implying that large porphyritic chondrules are fragmented preferentially. This is consistent with the relatively low percentage of porphyritic chondrules within the set of the largest chondrules (57%) compared to that within the set of the smallest chondrules (81%). Differences in mean size among chondrule textural types may be due mainly to parent‐body chondrule‐fragmentation events and not to chondrule‐formation processes in the solar nebula.     

Quantitative in situ XRD measurement of shock metamorphism in Martian meteorites using lattice strain and strain‐related mosaicity in olivine

All Martian meteorites have experienced shock metamorphism to some degree. We quantitatively determined shock‐related strain in olivine crystals to measure shock level and peak shock pressure experienced by five Martian meteorites. Two independent methods employing nondestructive in situ micro X‐ray diffraction (μXRD) are applied, i.e., (1) the lattice strain method, in which the lattice strain value (ε) for each olivine grain is derived from a Williamson–Hall plot using its diffraction pattern (peak width variation with diffraction angle) with reference to a best fit calibration curve of ε values obtained from experimentally shocked olivine grains; (2) the strain‐related mosaicity method, allowing shock stage to be estimated by measuring the streaking along the Debye rings of olivine grain diffraction spots to define their strain‐related mosaic spread, which can then be compared with olivine mosaicity in ordinary chondrites of known shock stage. In this study, both the calculated peak shock pressures and the estimated shock stages for Dar al Gani 476 (45.6 ± 0.6 GPa), Sayh al Uhaymir 005/8 (46.1 ± 2.2 GPa), and Nakhla (18.0 ± 0.6 GPa) compare well with literature values. Formal shock assessments for North West Africa 1068/1110 (53.9 ± 2.1 GPa) and North West Africa 6234 (44.6 ± 3.1 GPa) have not been reported within the literature; however, their calculated peak shock pressures fall within the range of peak shock pressures defining their estimated shock stages. The availability of nondestructive and quantitative μXRD methods to determine shock stage and peak shock pressure from olivine crystals provides a key tool for shock metamorphism analysis.     

NWA 10214—An LL3 chondrite breccia with an assortment of metamorphosed,shocked, and unique chondrite clasts

NWA 10214 is an LL3‐6 breccia containing ~8 vol% clasts including LL5, LL6, and shocked‐darkened LL fragments as well as matrix‐rich Clast 6 (a new kind of chondrite). This clast is a dark‐colored, subrounded, 6.1 × 7.0 mm inclusion, consisting of 60 vol% fine‐grained matrix, 32 vol% coarse silicate grains, and 8 vol% coarse opaque grains. The large chondrules and chondrule fragments are mainly Type IB; one small chondrule is Type IIA. Also present are one 450 × 600 μm spinel‐pyroxene‐olivine CAI and one 85 × 110 μm AOI. Clast 6 possesses a unique set of properties. (1) It resembles carbonaceous chondrites in having relatively abundant matrix, CAIs, and AOIs; the clast's matrix composition is close to that in CV3 Vigarano. (2) It resembles type‐3 OC in its olivine and low‐Ca pyroxene compositional distributions, and in the Fe/Mn ratio of ferroan olivine grains. Its mean chondrule size is within 1σ of that of H chondrites. The O‐isotopic compositions of the chondrules are in the ordinary‐ and R‐chondrite ranges. (3) It resembles type‐3 enstatite chondrites in the minor element concentrations in low‐Ca pyroxene grains and in having a high low‐Ca pyroxene/olivine ratio in chondrules. Clast 6 is a new variety of type‐3 OC, somewhat more reduced than H chondrites or chondritic clasts in the Netschaevo IIE iron; the clast formed in a nebular region where aerodynamic radial drift processes deposited a high abundance of matrix material and CAIs. A chunk of this chondrite was ejected from its parent asteroid and later impacted the LL body at low relative velocity.