Analysis of ordinary chondrites using powder X‐ray diffraction: 1. Modal mineral abundances

Abstract– Powder X‐ray diffraction (XRD) is used to quantify the modal abundances (in wt%) of 18 H, 17 L, and 13 LL unbrecciated ordinary chondrite falls, which represents the complete petrologic range of equilibrated ordinary chondrites (types 4–6). The XRD technique presents an effective alternative to traditional methods for determining modal abundances, such as optical point counting and electron microprobe phase (EMP) mapping. The majority of chondrite powders in this study were previously prepared for chemical characterization from 8 to 20 g of material, which is consistent with the suggested mass (10 g) necessary to provide representative sampling of ordinary chondrites. Olivine and low‐Ca pyroxene are the most abundant phases present, comprising one‐half to three‐fourths of total abundances, while plagioclase, high‐Ca pyroxene, troilite, and metal comprise the remaining XRD‐measured mineralogy. Pigeonite may also be present in some samples, but it is fitted using a high‐Ca pyroxene standard, so exact abundances cannot be measured directly using XRD. Comparison of XRD‐measured abundances with calculated Cross, Iddings, Pirsson, Washington (CIPW) normative abundances indicates that systematic discrepancies exist between these two data sets, particularly in olivine and high‐Ca pyroxene. This discrepancy is attributed to the absence of pigeonite as a possible phase in the CIPW normative mineralogy. Oxides associated with pigeonite are improperly allocated, resulting in overestimated normative olivine abundances and underestimated normative high‐Ca pyroxene abundances. This suggests that the CIPW norm is poorly suited for determining mineralogical modal abundances of ordinary chondrites.     

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.     

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.     

MÖssbauer spectroscopy,x-ray diffraction,and electron microprobe analysis of the New Haifa meteorite

Abstract— MÖssbauer spectroscopy, x-ray diffraction (XRD) measurements, and electron microprobe analysis (EMPA) have been carried out for the investigation of a newly fallen Sudanese meteorite named New Haifa. The room temperature MÖssbauer spectrum is fitted with three sextets and two doublets. The sextets are assigned to Fe in troilite, kamacite, and taenite, and the two doublets are assigned to Fe²⁺in olivine and pyroxene (no Fe³⁺was found). The microprobe trace of Ni concentration across a kamacite-taenite-kamacite area shows a high-Ni concentration at the interfaces between kamacite and taenite. From the microprobe analysis, olivine appears to have a constant composition, whereas pyroxene has a varying composition. The mole fractions of the Fe end members of olivine (fayalite) and pyroxene (ferrosilite) are found to be 23.5% and 23.2%, respectively. Accordingly, the New Haifa meteorite is classified as an ordinary L-type chondrite.     

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.     

Mineral compositions in Antarctic and Greenland micrometeorites

Abstract— The mineral compositions of 250 micrometeorites have been studied and olivines and low-calcium pyroxenes with crystals larger than 5 μm have been analyzed. While magnesium-rich grains dominate, the Fa content of olivine may reach 50% and the Fs content of pyroxene may reach 26%. The Ca and Mn of the olivine show no consistent trends with increasing Fe, but Cr shows a negative correlation. For low-Ca pyroxene, Al and Cr contents are generally higher than in pyroxenes of equilibrated chondrites but similar to those of highly unequilibrated chondrites. Calcium-bearing pyroxene, feldspar and chromite are rare in the micrometeorites which were selected because of their high Mg, Si, Fe and their low Ca and Al content. All these minerals are found as coarse-grained particles often with adhering iron-rich scoria or as clasts in fine-grained or scoriaceous micrometeorites. Apart from a few particles which could be the debris of ordinary chondrites, most micrometeorites probably come from a common source similar, but not identical to carbonaceous chondrites, as shown by their lower Ni and S content and their different oxygen isotopic composition assuming two measurements performed on olivine grains prove to be typical.     

Perceptive of the pyroxene-bearing micrometeorites and their relation to chondrites

We studied 149 pyroxenes from 69 pyroxene-bearing micrometeorites collected from deep-sea sediments of the Indian Ocean and South Pole Water Well at Antarctica, Amundsen-Scott South Pole station. The minor elements in pyroxenes from micrometeorites are present in the ranges as follows: MnO ~0.0–0.4 wt%, Al₂O₃ ~0.0–1.5 wt%, CaO ~0.0–1.0 wt%, Cr₂O₃ ~0.3–0.9 wt%, and FeO ~0.5–4 wt%. Their chemical compositions suggest that pyroxene-bearing micrometeorites are mostly related to precursors from carbonaceous chondrites rather than ordinary chondrites. The Fe/(Fe+Mg) ratio of the pyroxenes and olivines in micrometeorites shows similarities to carbonaceous chondrites with values lying between 0 and 0.2, and those with values beyond this range are dominated by ordinary chondrites. Atmospheric entry of the pyroxene-bearing micrometeorites is expected to have a relatively low entry velocity of <16 km s⁻¹ and high zenith angle (70–90°) to preserve their chemical compositions. In addition, similarities in the pyroxene and olivine mineralogical compositions between carbonaceous chondrites and cometary particles suggest that dust in the solar system is populated by materials from different sources that are chemically similar to each other. Our results on pyroxene chemical compositions reveal significant differences with those from ordinary chondrites. The narrow range in olivine and pyroxene chemical compositions are similar to those from carbonaceous chondrites, and a small proportion to ordinary chondrites indicates that dust is largely sourced from carbonaceous chondrite-type bodies.     

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.     

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.     

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.     

Characterization of Mason Gully (H5): The second recovered fall from the Desert Fireball Network

Mason Gully, the second meteorite recovered using the Desert Fireball Network (DFN), is characterized using petrography, mineralogy, oxygen isotopes, bulk chemistry, and physical properties. Geochemical data are consistent with its classification as an H5 ordinary chondrite. Several properties distinguish it from most other H chondrites. Its 10.7% porosity is predominantly macroscopic, present as intergranular void spaces rather than microscopic cracks. Modal mineralogy (determined via PS‐XRD, element mapping via energy dispersive spectroscopy [EDS], and X‐ray tomography [for sulfide, metal, and porosity volume fractions]) consistently gives an unusually low olivine/orthopyroxene ratio (0.67?0.76 for Mason Gully versus ~1.3 for typical H5 ordinary chondrites). Widespread “silicate darkening” is observed. In addition, it contains a bright green crystalline object at the surface of the recovered stone (diameter ≈ 1.5 mm), which has a tridymite core with minor α‐quartz and a rim of both low‐ and high‐Ca pyroxene. The mineralogy allows the calculation of the temperatures and ?(O₂) characterizing thermal metamorphism on the parent body using both the two‐pyroxene and the olivine‐chromite geo‐oxybarometers. These indicate that MG experienced a peak metamorphic temperature of ~900 °C and had a similar ?(O₂) to Kernouvé (H6) that was buffered by the reaction between olivine, metal, and pyroxene. There is no evidence for shock, consistent with the observed porosity structure. Thus, while Mason Gully has some unique properties, its geochemistry indicates a similar thermal evolution to other H chondrites. The presence of tridymite, while rare, is seen in other OCs and likely exogenous; however, the green object itself may result from metamorphism.     

A coordinated spectral, mineralogical, and compositional study of ordinary chondrites

Mineral compositions and abundances derived from visible/near-infrared (VIS/NIR or VNIR) spectra are used to classify asteroids, identify meteorite parent bodies, and understand the structure of the asteroid belt. Using a suite of 48 equilibrated (types 4-6) ordinary (H, L, and LL) chondrites containing orthopyroxene, clinopyroxene, and olivine, new relationships between spectra and mineralogy have been established. Contrary to previous suggestions, no meaningful correlation is observed between band parameters and cpx/(opx + cpx) ratios. We derive new calibrations for determining mineral abundances (ol/(ol + px)) and mafic silicate compositions (Fa in olivine, Fs in pyroxene) from VIS/NIR spectra. These calibrations confirm that band area ratio (BAR) is controlled by mineral abundances, while Band I center is controlled by mafic silicate compositions. Spectrally-derived mineralogical parameters correctly classify H, L and LL chondrites in ∼80% of cases, suggesting that these are robust relationships that can be applied to S(IV) asteroids with ordinary chondrites mineralogies. Comparison of asteroids and meteorites using these new mineralogical parameters has the advantage that H, L and LL chemical groups were originally defined on the basis of mafic silicate compositions.     

Infrared transmission spectra from 2.5 to 25 μm of various meteorite classes

Infrared transmission spectra from 53 meteorites in the spectral range from 2.5 to 25 μm were measured to permit comparisons with data of astronomical objects that are potential meteorite sources. Data were taken for 14 carbonaceous chondrites, 5 LL ordinary chondrites, 6 L ordinary chondrites, 10 H ordinary chondrites, 1 enstatite chondrite, 4 aubrites, 3 eucrites, 4 howardites, 1 diogenite, 1 mesosiderite, 2 nakhlites, 1 shergottite, and the anomalous achondrite Angra dos Reis. The CO and CV carbonaceous chondrites have spectra similar to each other, with 10-μm features characteristic of olivine. The CM carbonaceous chondrites have distinctive 10-μm features that are attributed to layer lattice silicates. Members of both the CI and CR classes have spectra distinct from those of other carbonaceous chondrites. The LL, L, and H ordinary chondrites have spectra that match those of olivine and pyroxene mixtures. The enstatite chondrites and enstatite achondrites (aubrites) all exhibit spectra diagnostic of the pyroxene enstatite. The angrite, howardites, aucrites, nakhlites, shergottite, and diogenite all have similar spectra also dominated by pyroxene. The single mesosiderite examined had a spectrum distinct from all the other meteorites.     

Compositional diversity of ordinary chondrites inferred from petrology,bulk chemical,and oxygen isotopic compositions of the lowest FeO ordinary chondrite,Yamato 982717

We performed a petrologic, geochemical, and oxygen isotopic study of the lowest FeO ordinary chondrite (OC), Yamato (Y) 982717. Y 982717 shows a chondritic texture composed of chondrules and chondrule fragments, and mineral fragments set in a finer grained, clastic matrix, similar to H4 chondrites. The composition of olivine (Fa_{11.17 ± 0.48 (1σ)}) and low‐Ca pyroxene (Fs_{11.07 ± 0.98 (1σ)}Wo_{0.90 ± 0.71(1σ)}) is significantly more magnesian than those of typical H chondrites (Fa_16.0‐20, Fs_14.5‐18.0), as well as other known low‐FeO OCs (Fa_12.8‐16.7; Fs_13‐16). However, the bulk chemical composition of Y 982717, in particular lithophile and moderately volatile elements, is within the range of OCs. The bulk siderophile element composition (Ni, Co) is within the range of H chondrites and distinguishable from L chondrites. The O‐isotopic composition is also within the range of H chondrites. The lack of reduction textures indicates that the low olivine Fa content and low‐Ca pyroxene Fs content are characteristics of the precursor materials, rather than the result of reduction during thermal metamorphism. We suggest that the H chondrites are more compositionally diverse than has been previously recognized.     

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.     

An in situ study of presolar grains and the fine-grained matrices of the Meteorite Hills 00526 and Queen Alexandra Range 97008 unequilibrated ordinary chondrites

Here we report in situ structural and chemical analyses of four presolar grains and the matrices of the Meteorite Hills (MET) 00526 L3.05 and Queen Alexandra Range (QUE) 97008 L3.05 unequilibrated ordinary chondrites (UOCs). The presolar grains in MET 00526 include one Fe-rich single crystal olivine, and one olivine grain that contains both amorphous and polycrystalline material. The single crystal olivine likely has origins in the circumstellar envelope (CSE) of a red giant branch (RGB) or asymptotic giant branch (AGB) star, and the amorphous/polycrystalline olivine has an O-isotopic composition consistent with origins in a type II supernova. The presolar grains from QUE 97008 are Fe rich and include one crystalline, stoichiometric olivine that contains a Ca-rich core and one crystalline, stoichiometric pyroxene grain, both of which have O-isotopic compositions consistent with origins in the CSEs of low-mass AGB/RGB stars. The matrices of both UOCs are mineralogically diverse with evidence for unaltered material in the form of amorphous silicates and a C-rich nanoglobule and altered material in the form of Ni-rich sulfides, abundant Fe-rich olivine, and Fe-Mg zoning in matrix silicates. No phyllosilicates were observed. The Fe-rich olivine grains are the dominant alteration phase in both UOCs and likely replaced primary amorphous silicates in the presence of an Fe-rich fluid during parent body alteration. Our work suggests that the ordinary and carbonaceous chondrites received a similar inventory of dust with comparable structures and chemistries.     

Spectral properties and mineral compositions of acapulcoite–lodranite clan meteorites: Establishing S‐type asteroid–meteorite connections

Except for asteroid sample return missions, measurements of the spectral properties of both meteorites and asteroids offer the best possibility of linking meteorite groups with their parent asteroid(s). Visible plus near‐infrared spectra reveal distinguishing absorption features controlled mainly by the Fe²⁺ contents and modal abundances of olivine and pyroxene. Meteorite samples provide relationships between spectra and mineralogy. These relationships are useful for estimating the olivine and pyroxene mineralogy of stony (S‐type) asteroid surfaces. Using a suite of 10 samples of the acapulcoite–lodranite clan (ALC), we have developed new correlations between spectral parameters and mafic mineral compositions for partially melted asteroids. A well‐defined relationship exists between Band II center and ferrosilite (Fs) content of orthopyroxene. Furthermore, because Fs in orthopyroxene and fayalite (Fa) content in olivine are well correlated in these meteorites, the derived Fs content can be used to estimate Fa of the coexisting olivine. We derive new equations for determining the mafic silicate compositions of partially melted S‐type asteroid parent bodies. Stony meteorite spectra have previously been used to delineate meteorite analog spectral zones in Band I versus band area ratio (BAR) parameter space for the establishment of asteroid–meteorite connections with S‐type asteroids. However, the spectral parameters of the partially melted ALC overlap with those of ordinary (H) chondrites in this parameter space. We find that Band I versus Band II center parameter space reveals a clear distinction between the ALC and the H chondrites. This work allows the distinction of S‐type asteroids as nebular (ordinary chondrites) or geologically processed (primitive achondrites).     

Oxygen isotopic and chemical composition of chromites in micrometeorites: Evidence of ordinary chondrite precursors

We identified 66 chromite grains from 42 of ~5000 micrometeorites collected from Indian Ocean deep‐sea sediments and the South Pole water well. To determine the chromite grains precursors and their contribution to the micrometeorite flux, we combined quantitative electron microprobe analyses and oxygen isotopic analyses by high‐resolution secondary ion mass spectrometry. Micrometeorite chromite grains show variable O isotopic compositions with δ¹⁸O values ranging from ?0.8 to 6.0‰, δ¹⁷O values from 0.3 to 3.6‰, and Δ¹⁷O values from ?0.9 to 1.6‰, most of them being similar to those of chromites from ordinary chondrites. The oxygen isotopic compositions of olivine, considered as a proxy of chromite in chromite‐bearing micrometeorites where chromite is too small to be measured in ion microprobe have Δ¹⁷O values suggesting a principal relationship to ordinary chondrites with some having carbonaceous chondrite precursors. Furthermore, the chemical compositions of chromites in micrometeorites are close to those reported for ordinary chondrite chromites, but some contribution from carbonaceous chondrites cannot be ruled out. Consequently, carbonaceous chondrites cannot be a major contributor of chromite‐bearing micrometeorites. Based on their oxygen isotopic and elemental compositions, we thus conclude with no ambiguity that chromite‐bearing micrometeorites are largely related to fragments of ordinary chondrites with a small fraction from carbonaceous chondrites, unlike other micrometeorites deriving largely from carbonaceous chondrites.     

The oxygen isotopic properties of olivines in the Semarkona ordinary chondrite

Abstract— In order to explore the origin of chondrules and the chondrites, the O isotopic compositions of nine olivine grains in seven chondrules from the primitive Semarkona LL3.0 chondrite have been determined by ion microprobe. The data plot in the same general region of the three-isotope plot as whole-chondrule samples from ordinary chondrites previously measured by other techniques. There are no significant differences between the O isotopic properties of olivine in the various chondrule groups in the present study, but there is a slight indication that the data plot at the ¹⁶O-rich end of the ordinary chondrite field. This might suggest that the mesostasis contains isotopically heavy O. The olivines in the present study have O isotopic compositions unlike the ¹⁶O-rich olivine grains from the Julesburg ordinary chondrite. Even though olivines in group A chondrules have several properties in common with them, the ¹⁶O-rich Julesburg olivines previously reported are not simply olivines from group A chondrules.