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.     

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).     

Mineralogical characterization of Baptistina Asteroid Family: Implications for K/T impactor source

Bottke et al. [Bottke, W.F., Vokrouhlicky, D., Nesvorný, D., 2007. Nature 449, 48–53] linked the catastrophic formation of Baptistina Asteroid Family (BAF) to the K/T impact event. This linkage was based on dynamical and compositional evidence, which suggested the impactor had a composition similar to CM2 carbonaceous chondrites. However, our recent study [Reddy, V., Emery, J.P., Gaffey, M.J., Bottke, W.F., Cramer, A., Kelley, M.S., 2009. Meteorit. Planet. Sci. 44, 1917–1927] suggests that the composition of (298) Baptistina is similar to LL-type ordinary chondrites rather than CM2 carbonaceous chondrites. This rules out any possibility of it being related to the source of the K/T impactor, if the impactor was of CM-type composition. Mineralogical study of asteroids in the vicinity of BAF has revealed a plethora of compositional types suggesting a complex formation and evolution environment. A detailed compositional analysis of 16 asteroids suggests several distinct surface assemblages including ordinary chondrites (Gaffey SIV subtype), primitive achondrites (Gaffey SIII subtype), basaltic achondrites (Gaffey SVII subtype and V-type), and a carbonaceous chondrite. Based on our mineralogical analysis we conclude that (298) Baptistina is similar to ordinary chondrites (LL-type) based on olivine and pyroxene mineralogy and moderate albedo. S-type and V-type in and around the vicinity of BAF we characterized show mineralogical affinity to (8) Flora and (4) Vesta and could be part of their families. Smaller BAF asteroids with lower SNR spectra showing only a ‘single’ band are compositionally similar to (298) Baptistina and L/LL chondrites. It is unclear at this point why the silicate absorption bands in spectra of asteroids with formal family definition seem suppressed relative to background population, despite having similar mineralogy.     

The M‐/X‐asteroid menagerie: Results of an NIR spectral survey of 45 main‐belt asteroids

Abstract– Diagnostic mineral absorption features for pyroxene(s), olivine, phyllosilicates, and hydroxides have been detected in the near‐infrared (NIR: approximately 0.75–2.50 μm) spectra for 60% of the Tholen‐classified ( Tholen 1984, 1989 ) M‐/X‐asteroids observed in this study. Nineteen asteroids (42%) exhibit weak Band I (approximately 0.9 μm) ± Band II (approximately 1.9 μm) absorptions, three asteroids (7%) exhibit a weak Band I (approximately 1.05–1.08 μm) olivine absorption, four asteroids (9%) display multiple absorptions suggesting phyllosilicate ± oxide/hydroxide minerals, one (1) asteroid exhibits an S‐asteroid type NIR spectrum, and 18 asteroids (40%) are spectrally featureless in the NIR, but have widely varying slopes. Tholen M‐asteroids are defined as asteroids exhibiting featureless visible‐wavelength (λ) spectra with moderate albedos ( Tholen 1989 ). Tholen X‐asteroids are also defined using the same spectral criterion, but without albedo information. Previous work has suggested spectral and mineralogical diversity in the M‐asteroid population ( Rivkin et al. 1995, 2000 ; Busarev 2002 ; Clark et al. 2004 ; Hardersen et al. 2005 ; Birlan et al. 2007 ; Ockert‐Bell et al. 2008, 2010 ; Shepard et al. 2008, 2010 ; Fornasier et al. 2010 ). The pyroxene‐bearing asteroids are dominated by orthopyroxene with several likely to include higher‐Ca clinopyroxene components. Potential meteorite analogs include mesosiderites, CB/CH chondrites, and silicate‐bearing NiFe meteorites. The Eos family, olivine‐bearing asteroids are most consistent with a CO chondrite analog. The aqueously altered asteroids display multiple, weak absorptions (0.85, 0.92, 0.97, 1.10, 1.40, and 2.30–2.50 μm) indicative of phyllosilicate ± hydroxide minerals. The spectrally featureless asteroids range from metal‐rich to metal‐poor with meteorite analogs including NiFe meteorites, enstatite chondrites, and stony‐iron meteorites.     

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.     

Spectral-compositional variations in the constituent minerals of mafic and ultramafic assemblages and remote sensing implications

The 0.3–2.6 m reflectance spectra of most mafic and ultramafic assemblages can best be interpreted by considering the spectra as being composed of mafic silicate spectra modified by the presence of opaques, such as ilmenite or magnetite, and plagioclase feldspar. The systematic spectral-compositional relationships for olivine, orthopyroxene, and clinopyroxene have been examined and it has been determined that absorption band wavelength positions are correlated with ferrous iron content. Binary mafic silicate mixtures are generally less well understood, but certain spectral features such as reflectance maxima and minima wavelength positions and absorption band areas can be used to quantify or at least constrain end member abundances and compositions. The addition of opaques to a mafic silicate assemblage lowers overall reflectance and band depths. This differs from the effects of increasing grain size which are to lower overall reflectance but increase band depths. Plagioclase is relatively transparent compared to mafic silicates and must be present in appreciable amounts (tens of percent) to be spectrally detectable. The reflectance spectra of most mafic and ultramafic assemblages are dominated by mafic silicate absorption features and analysis of their spectra on this basis allows constraints to be placed on properties such as end member abundances and compositions.     

Mineralogies and source regions of near-Earth asteroids

Near-Earth Asteroids (NEAs) offer insight into a size range of objects that are not easily observed in the main asteroid belt. Previous studies on the diversity of the NEA population have relied primarily on modeling and statistical analysis to determine asteroid compositions. Olivine and pyroxene, the dominant minerals in most asteroids, have characteristic absorption features in the visible and near-infrared (VISNIR) wavelengths that can be used to determine their compositions and abundances. However, formulas previously used for deriving compositions do not work very well for ordinary chondrite assemblages. Because two-thirds of NEAs have ordinary chondrite-like spectral parameters, it is essential to determine accurate mineralogies. Here we determine the band area ratios and Band I centers of 72 NEAs with visible and near-infrared spectra and use new calibrations to derive the mineralogies 47 of these NEAs with ordinary chondrite-like spectral parameters. Our results indicate that the majority of NEAs have LL-chondrite mineralogies. This is consistent with results from previous studies but continues to be in conflict with the population of recovered ordinary chondrites, of which H chondrites are the most abundant. To look for potential correlations between asteroid size, composition, and source region, we use a dynamical model to determine the most probable source region of each NEA. Model results indicate that NEAs with LL chondrite mineralogies appear to be preferentially derived from the ν₆ secular resonance. This supports the hypothesis that the Flora family, which lies near the ν₆ resonance, is the source of the LL chondrites. With the exception of basaltic achondrites, NEAs with non-chondrite spectral parameters are slightly less likely to be derived from the ν₆ resonance than NEAs with chondrite-like mineralogies. The population of NEAs with H, L, and LL chondrite mineralogies does not appear to be influenced by size, which would suggest that ordinary chondrites are not preferentially sourced from meter-sized objects due to Yarkovsky effect.     

Chemical and mineralogical compositions of two grains recovered from asteroid Itokawa

Two silicate grains (RB‐QD04‐0049 and RA‐QD02‐0064, whose estimated masses are 0.050 μg and 0.048 μg, respectively) recovered from the asteroid Itokawa by the Hayabusa spacecraft were studied for their mineralogical characteristics by synchrotron X‐ray diffraction and synchrotron X‐ray microtomography and further analyzed for their bulk chemical compositions by instrumental neutron activation analysis (INAA). According to X‐ray tomography, RB‐QD004‐0049 is composed of olivine, high‐Ca pyroxene, plagioclase, Ca‐phosphate, and troilite, whereas RA‐QD002‐0064 entirely consists of olivine. INAA data are consistent with these mineral compositions except for rare earth elements (REEs). Although the grain RB‐QD004‐0049 contains measurable REEs, which seems to be consistent with the presence of Ca‐phosphate, their abundances are anomalously high. Very low abundance of Co implies less than 0.1 mass% of metals in these two grains by calculation, which is in contrast to the result for the previously analyzed grain RA‐QD02‐0049 (Ebihara et al., 2011). FeO/Sc ratios of the grains fall within the range of those for ordinary chondrite olivines, implying that these grains are extraterrestrial in origin. FeO/MnO ratios also confirm this conclusion and further suggest that the Hayabusa grains analyzed in this study are similar to material found in LL chondrites rather than CK chondrites although olivines from LL and CK chondrites have similar Fa# (molar% of Fe relative to [Fe+Mg] in olivine) (~30) to those of the Hayabusa grains including the two grains analyzed in this study.     

Mafic silicate mapping on Mars: effects of palagonitic material, multiple mafic silicates, and spectral resolution

The visible to near-infrared spectral reflectance properties of intimate and areal pyroxene?+?palagonitic material mixtures as well as pure mafic silicates (low-calcium pyroxene, high-calcium pyroxene, pigeonite, olivine) and mixtures of these minerals were analyzed at high spectral resolution (5 nm) as well as with non-contiguous band passes equivalent to recent HST observations and the Pathfinder IMP in order to determine the quality and quantity of mineralogical information (end member compositions, abundances, and grain sizes) derivable in the presence of palagonitic material. In the case of pyroxene?+?palagonitic material mixtures, pyroxene is detectable at abundances as low as 10 wt%, and its composition can be constrained because (a) its diagnostic absorption feature (located near 1000 nm) persists even for high palagonitic material abundances, and (b) palagonitic material does not appreciably alter the wavelength position of this band (<4 nm variation). For broad band data (such as Pathfinder IMP band passes), different mafic silicates can be discriminated and palagonitic material abundances constrained using a variety of reflectance ratios and three-point “absorption band depths.” However, other properties of mafic silicate?±?palagonitic material assemblages, such as mafic silicate major element compositions, grain sizes, and end member abundances, generally cannot be rigorously quantified. The use of multiple reflectance ratios can, however, be used to identify relative changes in these properties, as most changes in mafic silicate?±?palagonitic material assemblage properties are characterized by a unique corresponding set of reflectance ratio variations. The observed spectral-assemblage property trends are consistent with those expected from the known spectral properties of the end members.     

Restriction of parent body heating by metal‐troilite melting: Thermal models for the ordinary chondrites

Ordinary chondrite meteorites contain silicates, Fe,Ni‐metal grains, and troilite (FeS). Conjoined metal‐troilite grains would be the first phase to melt during radiogenic heating in the parent body, if temperatures reached over approximately 910–960 °C (the Fe,Ni‐FeS eutectic). On the basis of two‐pyroxene thermometry of 13 ordinary chondrites, we argue that peak temperatures in some type 6 chondrites exceeded the Fe,Ni‐FeS eutectic and thus conjoined metal‐troilite grains would have begun to melt. Melting reactions consume energy, so thermal models were constructed to investigate the effect of melting on the thermal history of the H, L, and LL parent asteroids. We constrained the models by finding the proportions of conjoined metal‐troilite grains in ordinary chondrites using high‐resolution X‐ray computed tomography. The models show that metal‐troilite melting causes thermal buffering and inhibits the onset of silicate melting. Compared with models that ignore the effect of melting, our models predict longer cooling histories for the asteroids and accretion times that are earlier by 61, 124, or 113 kyr for the H, L, and LL asteroids, respectively. Because the Ni/Fe ratio of the metal and the bulk troilite/metal ratio is higher in L and LL chondrites than H chondrites, thermal buffering has the greatest effect in models for the L and LL chondrite parent bodies, and least effect for the H chondrite parent. Metal‐troilite melting is also relevant to models of primitive achondrite parent bodies, particularly those that underwent only low degrees of silicate partial melting. Thermal models can predict proportions of petrologic types formed within an asteroid, but are systematically different from the statistics of meteorite collections. A sampling bias is interpreted to explain these differences.     

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.     

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.     

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.     

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.     

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

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

Visible‐IR and Raman microspectroscopic investigation of three Itokawa particles collected by Hayabusa: Mineralogy and degree of space weathering based on nondestructive analyses

Hayabusa‐returned samples offer a unique perspective for understanding the link between asteroids and cosmomaterials available in the laboratory, and provide insights on the early stages of surface space weathering. This study characterizes the mineralogy and the extent of space weathering of the three Itokawa particles RA‐QD02‐0163, RA‐QD02‐0174, and RA‐QD02‐0213 provided by JAXA to our consortium. We report here a series of results based on nondestructive analyses through visible‐near‐infrared reflectance and Raman spectroscopy. Results were obtained on the raw particles, both in their original containers and deposited on diamond windows. Identification of the minerals, characterization of their elemental compositions, and measurements of their relative abundances were led through Raman spectroscopy in punctual and automatic mode. Reflectance spectra in the visible and near‐IR wavelengths constrain the mineralogy of the grains and allow direct comparison with the surface of Itokawa. The spectra reflect the extent of space weathering experienced by the three particles. Particle RA‐QD02‐0163 consists of a heterogeneous mixture of minerals: olivine (Fo₇₆) dominates an assemblage with both Ca‐rich (En₅₀, Wo₅₀) and Ca‐poor (En₈₅) pyroxenes. The elemental compositions of the silicates are consistent with those previously reported for distinct Hayabusa particles. Particles RA‐QD‐0174 and RA‐QD02‐0213 are solely composed of olivine, whose chemical composition is similar to that observed in RA‐QD02‐0163. It has been previously shown that the S‐type asteroid 25143 Itokawa is a breccia of poorly equilibrated LL4 and highly equilibrated LL5 and LL6 materials. The three particles studied here can be related to the least metamorphosed lithology (LL4) based on the high forsterite content of the olivine. Neither carbonaceous matter nor hydrated minerals were detected through Raman on the three allocated particles. The NIR‐VIS reflectance (incidence = 45°, light collection at e = 0°) spectra of the three particles, in particular the 1 μm band, are consistent with the presence of both olivine and pyroxene detected via Raman. The spectra of particles RA‐QD02‐0163 and RA‐QD02‐0213 are also fully compatible with the ground‐based observations of asteroid (25143) Itokawa in terms of both spectral features and slope. By contrast, particle RA‐QD02‐0174 has a similar 1 μm band depth but higher (redder) spectral slope than the surface of Itokawa. This probably reveals a variable extent of space weathering among the regolith particles. RA‐QD02‐0174 may contain a higher amount of nanophase metallic iron and nanophase FeS. Such phases are products by space weathering induced by solar wind, previously detected on other Itokawa particles.     

Noble gases and mineralogy of meteorites from China and the Grove Mountains,Antarctica: A 0.05 Ma cosmic ray exposure age of GRV 98004

Abstract— We determined the mineralogical and chemical characteristics and the He, Ne, and Ar isotopic abundances of 2 meteorites that fell in China and of 2 meteorites that were recovered by the 15th Chinese Antarctic Research Expedition. Guangmingshan (H5), Zhuanghe (H5), and Grove Mountain (GRV) 98002 (L5) yield cosmic ray exposure (CRE) ages of 68.7 ± 10.0 Ma, 3.8 ± 0.6 Ma, and 17.0 ± 2.5 Ma, respectively. These ages are within the range typically observed for the respective meteorite types. GRV 98004 (H5) had an extremely short parent body‐Earth transfer time of 0.052 ± 0.008 Ma. Its petrography and mineral chemistry are indistinguishable from other typical H5 chondrites. Only 3 other meteorites exist with similarly low CRE ages: Farmington (L5), Galim (LL6), and ALH 82100 (CM2). We show that several asteroids in Earth‐crossing orbits, or in the main asteroid belt with orbits close to an ejection resonance, are spectrally matching candidates and may represent immediate precursor bodies of meteorites with CRE ages ≤0.1 Ma.     

Application of Mössbauer spectroscopy,multidimensional discriminant analysis,and Mahalanobis distance for classification of equilibrated ordinary chondrites

Mössbauer spectra of equilibrated ordinary chondrites consist of two doublets due to paramagnetic iron present in olivines and pyroxenes and two sextets due to magnetically ordered iron present in metallic phases and troilite. The spectral areas of the different mineralogical phases found by Mössbauer spectroscopy in meteorites are proportional to the number of iron atoms in this mineralogical phase. This property of Mössbauer spectra can be the basis for constructing a method for the classification of ordinary chondrites. This idea was first explored at the Mössbauer Laboratory in Kanpur. This group suggested a qualitative method based on 2‐dimensional plots of Mössbauer spectral areas and thus classified properly some meteorites. We constructed a quantitative method using Mössbauer spectral areas, multidimensional discriminant analysis, and Mahalanobis distance (4M method) to determine the probability of a meteorite to be of type H, L, or LL. Based on 59 Mössbauer spectra, we calculated by the 4M method, S _cluster , the level of similarity of the Goronyo meteorite to the clusters. On the plot of ferrosilite versus fayalite, the point representing Goronyo is located on the border between H and L areas. Calculated by the 4M method, the meteorite Goronyo is 32% similar to type H, 75% to type L, and 11% to type LL. Additional mineralogical analyses suggested that the Goronyo meteorite would be classified as type L, although it was originally reported as type H in the Meteoritical Bulletin Database.     

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.     

Results of statistical analysis of primary components concentrations in bulk chemical composition of ordinary chondrite groups

We used two different methods of statistical analysis—cluster analysis and principal component analysis—to analyze the concentrations of principal chemical components (Si, Mg, Ca, Fe, Ni) and Co in ordinary chondrites. The analysis is based predominantly on published data (metadata). In total, chemical composition data from 646 ordinary chondrites were used in the statistical analysis. The aim of this analysis was to establish whether it would be possible or not to distinguish H, L, and LL chondrites based on the concentrations of major elements and Co in their bulk chemical compositions. It was also important to determine what conclusions such an analysis could enable to draw about matter differentiation in the formation environments of primordial parent bodies of particular ordinary chondrite groups (H, L, and LL). Another aim of the statistical analysis was to determine whether the distribution of Fe and Ni (with Co admixtures) is independent of petrographic types within particular groups of chondrites. This is of crucial importance for determining the distribution of FeNi(Co) ore occurrences in potential extraterrestrial deposits on modern asteroids—the sources of ordinary chondrites. The obtained results of statistical analyses confirmed that a clear-cut distinction between particular groups of ordinary chondrites is only possible for group H, while distinguishing L chondrites from LL chondrites is not always obvious. The results of the statistical analyses relating to the question of the possible existence of several primordial parent bodies (formation environments) of each group of ordinary chondrites are consistent with the results of contemporary astronomical spectroscopy research. What is particularly interesting is obtaining indications of the existence of common formation environments of the matter of L and LL chondrites, possibly on a few primordial parent bodies. The statistical analyses indicate that there is no correlation between the concentration of principal chemical components and the petrographic type of ordinary chondrites. This proves homogenous distributions of these elements within the parent bodies of each group of ordinary chondrites. Hence, the distribution of these elements in individual present-day asteroids is also homogenous.