Characterization of the 1.2 μm M1 pyroxene band: Extracting cooling history from near‐IR spectra of pyroxenes and pyroxene‐dominated rocks

Abstract— The 1.2 μm band in near‐infrared spectra of pyroxenes results from Fe²⁺in the M1 crystallographic site. The distribution of Fe and Mg between the M1 and M2 sites is in part a function of the cooling rate and thermal history of a pyroxene. Combining near‐infrared and Mössbauer spectra for a series of compositionally controlled synthetic Mg, Fe, Ca pyroxenes, we quantify the strength of the 1.2 μm band as a function of Fe²⁺in the M1 site. Near‐infrared spectra are deconvolved into component absorptions that can be assigned to the M1 and M2 sites using the modified Gaussian model. The relative strength of the 1.2 μm band is shown to be directly related to the amount of Fe²⁺in the M1 site measured by Mössbauer spectroscopy. The strength of the 1.2 μm band relative to the combined strengths of the 1.2 and 2 μm bands, or the M1 intensity ratio, is calculated for 51 howardite, eucrite, and diogenite (HED) meteorites. Diogenites and cumulate eucrites exhibit the lowest M1 intensity ratios, consistent with their formation as slowly cooled cumulates. Basaltic eucrites exhibit a large range of M1 intensity ratios, all of which are consistently higher than the diogenites and cumulate eucrites. This example illustrates how the M1 intensity ratio can be a used as a tool for characterizing the cooling history of remotely detected pyroxene‐dominated rocks.     

The 506 nm absorption feature in pyroxene spectra: Nature and implications for spectroscopy-based studies of pyroxene-bearing targets

High-resolution (0.34 nm) reflectance spectra of a suite of terrestrial ortho- and clinopyroxenes were characterized in the 506-nm region. This region exhibits absorption bands attributed to spin-forbidden transitions in Fe²⁺ located in the M2, and possibly M1, crystallographic site(s). The most intense absorption bands (up to 3.8% deep in <45 μm fractions) are present in low Ca-content orthopyroxene spectra. This region exhibits two (spectral Group I) or more (spectral Group II) absorption bands in the 500-515 nm interval. Group I spectra are associated with the lowest Ca-content samples. For orthopyroxenes, the number of constituent absorption bands and band depths vary as a function of Ca content; increasing Ca content results the appearance of more than two absorption bands and a general reduction in band depths, offsetting an expected increase in band depth with increasing Fe²⁺ content; band depths may also be reduced due to the long wavelength wing of ultraviolet region Fe-O charge transfer absorptions. Band depths and shapes in this region are also a function of grain size, with the strongest bands appearing for larger grain sizes - in the 90-250 μm range. The number and position of constituent absorption bands can be used to constrain factors such as cooling rates, as expressed in the formation of Guinier-Preston zones versus coarser-grained augite exsolution lamellae. Band depths in the spectra of fine-grained (<45 μm) clinopyroxenes do not exceed 1% and are generally lowest for spectral type A clinopyroxenes, where most of the Fe²⁺ is present in the M1 crystallographic site. The appearance of the 506 nm band in the spectra of pyroxene-bearing asteroids can be used to constrain pyroxene composition and structure. The results of this study suggest that detailed analysis of absorption features in the 506 nm region is a powerful tool for determining the composition and structure of pyroxenes. The spectral resolution of the VIR-MS spectrometer aboard the Dawn spacecraft - which will examine Asteroid 4 Vesta, a body possessing surficial pyroxenes - will be sufficient to provide some constraints on pyroxene composition.     

Infrared micro-spectroscopy of the martian meteorite Zagami: Extraction of individual mineral phase spectra

Zagami, a well characterized SNC meteorite, represents a reference sample to verify the feasibility of the non-destructive infrared micro-spectroscopy technique to extract spectral signatures from individual mineral phases in a meteorite sample. For the first time individual infrared spectra of the major mineral phases, in the 6000-600 cm⁻¹ (1.67-16.7 μm) spectral interval, whose identification is confirmed by energy dispersive X-ray analysis and backscattered imaging, are measured. The signatures of the main mineral phases we identified in the Zagami chip are: (1) maskelynite characterized by broad and smooth SiO vibrational bands in the 1000 cm⁻¹ spectral region; (2) crystalline pyroxenes showing well defined fine structures; and (3) an oxide mineral phase with an almost featureless and flat spectrum. In the part of the spectrum centered around 2 μm, by analyzing the different positions of the Fe²⁺ bands, we were able to discern the high-Ca from the low-Ca pyroxene phases. This result demonstrates that by means of the infrared micro-spectroscopy technique it is possible to retrieve directly the composition of pyroxenes in the En-Fs-Wo system, without relying on the use of deconvolution techniques. In addition IR signatures due to water and aliphatic hydrocarbons were observed to be more abundant in the pyroxenes than in maskelynite. This could be an indication that the organic and water signatures are due to indigenous compounds in Zagami rather than laboratory contamination, however, further investigations are necessary before this conclusion can be confirmed.     

Polarized absorption spectra of single crystals of lunar pyroxenes and olivines

Measurements have been made of the polarized absorption spectra (360-2200 nm.) of compositionally zoned pyroxene minerals in rocks 10045, 10047 and 10058 and olivines in rocks 10020 and 10022. Specimens in the form of petrographic thin sections were mounted on polarizing microscopes equipped with three-axis universal stage attachments and inserted into a Cary 17 spectrophotometer. The Apollo 11 pyroxenes with relatively high Ti/Fe ratios were chosen initially to investigate the presence of crystal field spectra of Fe²⁺ and Ti³⁺ ions in the minerals.Broad intense bands at about 1000 and 2100 nm. arise from spin-allowed, polarization-dependent transitions in Fe²⁺ ions in pyroxenes. Several weak sharp peaks occur in the visible region. Peaks at 402, 425, 505, 550 and 585 nm. represent spin-forbidden transitions in Fe²⁺ ions, while broader bands at 460–470 nm. and 650–660 nm. are attributed to Ti³⁺ ions. Charge transfer bands, which in terrestrial pyroxenes often extend into the visible region, are displaced to shorter wavelengths in lunar pyroxenes. This feature correlates with the absence of Fe³⁺ ions in these minerals. The magnitudes of the intensity ratios: band 465 nm. (Ti³⁺) to band 1000 nm. (Fe²⁺) are similar to Ti/Fe ratios from lunar pyroxene bulk chemical analyses, suggesting that an appreciable amount of titanium occurs as Ti³⁺ ions in the lunar pyroxenes. The 505 nm. spin-forbidden peak in Fe²⁺, together with absorption at 465 nm. by Ti³⁺, contribute to the pink or pale reddish-brown colors of lunar pyroxenes in transmitted lights.The absorption spectral measurements not only provide information on the redox behavior and crystal chemistry of lunar pyroxenes, but also form a basis for interpreting spectral reflectivity properties of lunar rocks and the Moon's surface.     

Near‐infrared spectra of clinopyroxenes: Effects of calcium content and crystal structure

Abstract– Pyroxenes are among the most common minerals in the solar system and are ideally suited for remote geochemical analysis because of the sensitivity of their distinctive spectra to mineral composition. Fe²⁺ is responsible for the dominant pyroxene absorptions in the visible and near‐infrared, but substitutions of other cations such as Ca²⁺ change the crystal structure and site geometries and thus the crystal field splitting energies of the Fe cations. To define spectral systematics resulting from major pyroxene cations (Ca²⁺, Mg²⁺, and Fe²⁺), we focus on a suite of pyroxenes synthesized with only Ca²⁺, Mg²⁺, and Fe²⁺ in the two octahedral sites, specifically examining the effect of Ca²⁺ on pyroxene absorption bands. The modified Gaussian model is used to deconvolve pyroxene spectra into component bands that can then be linked directly to crystal field absorptions. In orthopyroxenes and low‐Ca clinopyroxenes, Ca²⁺‐content has a strong and predictable effect on the positions of the absorption bands. At a threshold of Wo₃₀, the crystal field environment stagnates and the M2 bands cease to change significantly as more Ca²⁺ is added. At Wo₅₀, when most of the M2 sites are filled by Ca²⁺, band positions do not change drastically, although the presence and strengths of the 1 and 2 μm bands are affected by even trace amounts of Fe²⁺ in the M2 site. It is thus apparent that next‐nearest neighbors and the distortions they impose on the pyroxene lattice affect the electronic states around the Fe²⁺ cations and control absorption band properties.     

2–16 μm spectroscopy of micron-sized enstatite (Mg,Fe)2Si2O6 silicates from primitive chondritic meteorites

We present mid-infrared spectra from individual enstatite silicate grains separated from primitive type 3 chondritic meteorites. The 2–16 μm transmission spectra were taken with microspectroscopic Fourier-transform infrared (FT-IR) techniques as part of a project to produce a data base of infrared spectra from minerals of primitive meteorites for comparison with astronomical spectra. In general, the wavelength of enstatite bands increases with the proportion of Fe. However, the wavelengths of the strong En₁₀₀ bands at 10.67 and 11.67 decrease with increasing Fe content. The 11.67-μm band exhibits the largest compositional wavelength shift (twice as large as any other). Our fits of the linear dependence of the pyroxene peaks indicate that crystalline silicate peaks in the 10-μm spectra of Herbig AeBe stars, HD 179218 and 104237, are matched by pyroxenes of En₉₀₋₉₂ and En₇₈₋₈₀, respectively. If these simplistic comparisons with the astronomical grains are correct, then the enstatite pyroxenes seen in these environments are more Fe-rich than are the forsterite (Fo₁₀₀) grains identified in the far-infrared which are found to be Mg end-member grains. This differs from the general composition of type 3 chondritic meteoritic grains in which the pyroxenes are more Mg-rich than are the olivines from the same meteorite.     

Axtell and Allende: A Mössbauer spectroscopic study

Abstract— Mössbauer spectra showed the CV3 oxidized subgroup meteorites Allende and Axtell to be similar in olivine content and in a surprising lack of pronounced magnetic components, but different in Fe³⁺ phases. One atypical Allende sample showed an 8% area under the curve for magnetite, which is still less than a reported value for a CV3 reduced subgroup member. Allende's unusual Fe³⁺ spectral region distinguishes it from most other stony meteorites and is difficult to fit to known mineral parameters.     

Ultraviolet spectral reflectance properties of common planetary minerals

Ultraviolet spectral reflectance properties (200-400 nm) of a large number of minerals known or presumed to exist on the surfaces of Mars, the Moon, and asteroids, and in many meteorites, were investigated. Ultraviolet reflectance spectra (200-400 nm) of these minerals range from slightly blue-sloped (reflectance decreasing toward longer wavelengths) to strongly red-sloped (reflectance increasing toward longer wavelengths). Most exhibit one or two absorption features that are attributable to FeO charge transfers involving Fe³⁺ or Fe²⁺. The UV region is a very sensitive indicator of the presence of even trace amounts (<0.01 wt%) of Fe³⁺ and Fe²⁺. The major Fe³⁺O absorption band occurs at shorter wavelengths (∼210-230 nm), and is more intense than the major Fe²⁺O absorption band (∼250-270 nm). Ti-bearing minerals, such as ilmenite, rutile and anatase exhibit UV absorption bands attributable to Ti⁴⁺O charge transfers. While the positions of metal-O charge transfer bands sometimes differ for different minerals, the variation is often not diagnostic enough to permit unique mineral identification. However, iron oxides and oxyhydroxides can generally be distinguished from Fe-bearing silicates in the 200-400 nm region on the basis of absorption band positions. Within a given mineral group (e.g., low-calcium pyroxene, olivine, plagioclase feldspar), changes in Fe²⁺ or Fe³⁺ abundance do not appear to result in a measurable change in absorption band minima positions. Absorption band positions can vary as a function of grain size, however, and this variation is likely due to band saturation effects. The intensity of metal-O charge transfers means that some minerals will exhibit saturated UV absorption bands even for fine-grained (<45 μm) powders. In cases where absorption bands are not saturated (e.g., Fe²⁺O bands in some plagioclase feldspars and pyroxenes), changes in Fe²⁺ content do not appear to cause variations in band position. In other minerals (e.g., olivine), changes in band positions are correlated with compositional and/or grain size variations, but this is likely due to increasing band saturation rather than compositional variations. Overall, we find that the UV spectral region is sensitive to different mineral properties than longer wavelength regions, and thus offers the potential to provide complementary capabilities and unique opportunities for planetary remote sensing.     

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).     

Spectroscopic analysis of Martian meteorite Allan Hills 84001 powder and applications for spectral identification of minerals and other soil components on Mars

Abstract— Spectroscopic measurement and analysis of Martian meteorites provide important information about the mineralogy of Mars, as well as necessary ground-truths for deconvolving remote sensing spectra of the Martian surface rocks. The spectroscopic properties of particulate ALH 84001 from 0.3 to 25 μm correctly identify low-Ca pyroxene as the dominant mineralogy. Absorption bands due to electronic transitions of ferrous iron are observed at 0.94 and 1.97 μm that are typical for low-Ca pyroxene. A strong, broad water band is observed near 3 μm that is characteristic of the water band typically associated with pyroxenes. Weaker features near 4.8, 5.2 and 6.2 μm are characteristic of particulate low-Ca pyroxene and can be distinguished readily from the features due to high-Ca pyroxene and other silicate minerals. The reflectance minimum occurs near 8.6 μm for the ALH 84001 powder, which is more consistent with high-Ca pyroxene and augite than low-Ca pyroxene. The dominant mid-infrared (IR) spectral features for the ALH 84001 powder are observed near 9 and 19.5 μm; however, there are multiple features in this region. These mid-IR features are generally characteristic of low-Ca pyroxene but cannot be explained by low-Ca pyroxene alone. Spectral features from 2.5–5 μm are typically associated with water, organics and carbonates and have been studied in spectra of the ALH 84001, split 92 powder and ALH 84001, splits 92 and 271 chip surfaces. Weak features have been identified near 3.5 and 4 μm that are assigned to organic material and carbonates. Another feature is observed at 4.27 μm in many surface spots and in the powder but has not yet been uniquely identified. Spectroscopic identification of minor organic and carbonate components in this probable piece of Mars suggests that detection of small amounts of organics and carbonates in the Martian surface regolith would also be possible using visible-infrared hyperspectral analyses. Laboratory spectroscopic analysis of Martian meteorites provides a unique opportunity to identify the spectral features of minerals and other components while they are embedded in their natural medium.     

NIR spectral trends of HED meteorites: Can we discriminate between the magmatic evolution, mechanical mixing and observation geometry effects?

The Howardite–Eucrite–Diogenite (HED) suite is a family of differentiated meteorites that provide a unique opportunity to study the differentiation of small bodies. The likely parent-body of this meteorite group, (4) Vesta is presently under study by the Dawn mission, scrutinizing its surface in the visible and NIR infrared range. Here, we discuss how well the magmatic trends observed in HED might be retrieved from NIR spectroscopy, by studying laboratory spectra of 10 HED meteorites together with spectra from the RELAB database. We show that although an exsolution process did occur for most eucrites (i.e. decomposition of a primary calcic pyroxene into a high-Ca and low-Ca pyroxene), it does not affect the “bulk pyroxene” trend retrieved from the location of the pyroxene crystal field bands (Band I with a maximum of absorption around at about 1 μm and Band II around 2 μm). Absolute values of the chemical composition appears however to deviate from the expected chemical composition. We show that mechanical mixture (i.e. impact gardening) will produce a linear mixing in the pyroxenes band position diagram (Band I position vs Band II position). This diagram also reveals that howardite are not pure mixtures of an average eucrite and average diogenite. Because asteroid surfaces are expected to show topography, we also study the effect of observation geometry on the NIR spectra of an eucrite and a diogenite by measuring the bi-directional reflectance spectra from 0.4 to 4.6 μm. Results show that these meteorites tend to act as forward scatterers, leading to a decrease of integrated band area (relative to the continuum) at high phase angles. The position of the two strong crystal field bands shows only small variability with observation geometry. Retrieval of the magmatic trends from the Band I vs Band II diagram should not be affected by observation geometry effects. Finally we performed NIR reflectance measurement on olivine diogenites. The presence of olivine can be suggested by using the Band Area Ratio vs Band I diagram, but this phase might affect the retrieval of pyroxene composition from the position of Band I and Band II.     

Detection of ferric iron in an exsolved lunar pyroxene using electron energy loss spectroscopy (EELS): Implications for space weathering and redox conditions on the Moon

To shed light on the mechanism of formation of nanophase iron particles (npFe) in space-weathered materials from airless bodies, we analyzed exsolved and unexsolved space-weathered lunar pyroxenes from Apollo 17 sample 71501. The exsolved pyroxene allowed for the observation of the effects of space weathering on similar mineral phases with variable composition. Using coordinated scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy and electron energy loss spectroscopy (EELS), we determined that two coexisting pyroxenes in the exsolved grain showed systematic variations in response to space weathering, despite equivalent exposure conditions. The npFe in the space-weathered rim of augite lamellae were smaller and fewer than the npFe in the rim of pigeonite lamellae. EELS spectrum imaging revealed the presence and heterogeneous distribution of Fe⁰, Fe²⁺, and Fe³⁺ in the exsolved pyroxene. Metallic iron occurred in the npFe, a mixture of Fe²⁺ and Fe³⁺ occurred in the pigeonite lamellae, and the augite lamellae contained virtually all Fe³⁺. Approximately 50% of the total Fe measured in the exsolved pyroxene grain was ferric. Partitioning of Fe²⁺ and Fe³⁺ among the lamellae is invoked to explain the difference in npFe development in pigeonite and augite. The results of this study, the first to identify Fe³⁺ in a crystalline lunar ferromagnesian silicate, have implications for our understanding of how space weathering might proceed in oxidized phases. Furthermore, the discovery of an Fe³⁺-rich pyroxene also supports attribution of the 0.7 μm absorption feature observed in Galileo Solid State Imager data to oxidized Fe in clinopyroxenes.     

Micro Raman spectroscopy of amphiboles and pyroxenes in the martian meteorites Zagami and Lewis Cliff 88516

Abstract— We studied micro Raman spectroscopy of amphiboles and pyroxenes in the martian meteorites Zagami and Lewis Cliff (LEW) 88516. The obtained Raman spectra of the amphiboles are similar to those of kaersutite, reconfirming the previous studies that they are kaersutitic amphiboles enriched in Ca, Al, and Ti. Even though actinolite belongs to the same amphibole group (calcic amphibole) as kaersutite, the Raman spectra of terrestrial actinolite are distinct from those of kaersutite, probably reflecting complex amphibole crystal structures. The Al‐Ti‐rich pyroxene observed in the magmatic inclusions within LEW 88516 olivine is compositionally similar to kaersutite but shows Raman spectra nearly identical to the regular pyroxene rather than amphibole. In contrast to amphibole, this will be due to relatively simple crystal structures of pyroxene. Thus, the Raman spectra of Al‐Ti‐rich phases in the martian meteorites are distinct between kaersutite and Al‐Ti‐rich pyroxene, and this study demonstrates that micro Raman spectroscopy is one of the best tools to perform mineralogical characterization of mineral phases in martian meteorites.     

Ferric iron in SNC meteorites as determined by Mössbauer spectroscopy: Implications for martian landers and martian oxygen fugacity

Abstract— Mössbauer spectra of martian meteorites are currently of great interest due to the Mössbauer spectrometers on the Athena mission MER rovers as well as the European Space Agency Mars Express mission, with its Beagle 2 payload. Also, considerable current effort is being made to understand the oxygen fugacity of martian magmas because of the effect of fO₂ on mineral chemistry and crystallization processes. For these 2 reasons, the present study was conceived to acquire room temperature Mössbauer spectra of mineral separates and whole rock samples of 10 SNC meteorites. The results suggest that mineral identification using remote application of this technique will be most useful when the phases present have distinctive parameters arising from Fe in very different coordination polyhedra; for example, pyroxene coexisting with olivine can be discriminated easily, but opx versus cpx cannot. The MER goal of using Mössbauer spectroscopy to quantify the relative amounts of individual mineral species present will be difficult to satisfy if silicates are present because the lack of constraints on wt% FeO contents of individual silicate phases present will make modal calculations impossible. The remote Mössbauer spectroscopy will be most advantageous if the rocks analyzed are predominantly oxides with known stoichiometries, though these phases are not present in the SNCs. As for the detection of martian oxygen fugacity, no evidence exists in the SNC samples studied of a relationship between Fe³⁺ content and fO₂ as calculated by independent methods. Possibly, all of the Fe³⁺ observed in olivine is the result of dehydrogenation rather than oxidation, and this process may also be the source of all the Fe³⁺ observed in pyroxene. The observed Fe³⁺ in pyroxene also likely records an equilibrium between pyroxene and melt at such low fO₂ that little or no Fe³⁺ would be expected.     

Exploration of faint absorption bands in the reflectance spectra of the asteroids by method of optimal smoothing: Vestoids

An optimization method of smoothing noisy spectra was developed to investigate faint absorption bands in the visual spectral region of reflectance spectra of asteroids and the compositional information derived from their analysis. The smoothing algorithm is called “optimal” because the algorithm determines the best running box size to separate weak absorption bands from the noise. The method is tested for its sensitivity to identifying false features in the smoothed spectrum, and its correctness of forecasting real absorption bands was tested with artificial spectra simulating asteroid reflectance spectra. After validating the method we optimally smoothed 22 vestoid spectra from SMASS1 [Xu, Sh., Binzel, R.P., Burbine, T.H., Bus, S.J., 1995. Icarus 115, 1-35]. We show that the resulting bands are not telluric features. Interpretation of the absorption bands in the asteroid spectra was based on the spectral properties of both terrestrial and meteorite pyroxenes. The bands located near 480, 505, 530, and 550 nm we assigned to spin-forbidden crystal field bands of ferrous iron, whereas the bands near 570, 600, and 650 nm are attributed to the crystal field bands of trivalent chromium and/or ferric iron in low-calcium pyroxenes on the asteroids' surface. While not measured by microprobe analysis, Fe³⁺ site occupancy can be measured with Mössbauer spectroscopy, and is seen in trace amounts in pyroxenes. We believe that trace amounts of Fe³⁺ on vestoid surfaces may be due to oxidation from impacts by icy bodies. If that is the case, they should be ubiquitous in the asteroid belt wherever pyroxene absorptions are found. Pyroxene composition of four asteroids of our set is determined from the band position of absorptions at 505 and 1000 nm, implying that there can be orthopyroxenes in all range of ferruginosity on the vestoid surfaces. For the present we cannot unambiguously interpret of the faint absorption bands that are seen in the spectra of 4005 Dyagilev, 4038 Kristina, 4147 Lennon, and 5143 Heracles. Probably there are other spectrally active materials along with pyroxenes on the surfaces of these asteroids.     

Spectral reflectance‐compositional properties of spinels and chromites: Implications for planetary remote sensing and geothermometry

Abstract— Reflectance spectra of spinels and chromites have been studied as a function of composition. These two groups of minerals are spectrally distinct, which relates largely to differences in the types of major cations present. Both exhibit a number of absorption features in the 0.3–26 μm region that show systematic variations with composition and can be used to quantify or constrain certain compositional parameters, such as cation abundances, and site occupancies. For spinels, the best correlations exist between Fe²⁺ content and wavelength positions of the 0.46, 0.93, 2.8, Restrahelen, 12.3, 16.2, and 17.5 μm absorption features, Al and Fe³⁺ content with the wavelength position of the 0.93 μm absorption feature, and Cr content from the depth of the absorption band near 0.55 μm. For chromites, the best correlations exist between Cr content and wavelength positions of the 0.49, 0.59, 2, 17.5, and 23 μm absorption features, Fe²⁺ and Mg contents with the wavelength position of the 1.3 μm absorption feature, and Al content with the wavelength position of the 2 μm absorption feature. At shorter wavelengths, spinels and chromites are most readily distinguished by the wavelength position of the absorption band in the 2 μm region (<2.1 μm for spinels, >2.1 μm for chromite), while at longer wavelengths, spectral differences are more pronounced. The importance of being able to derive compositional information for spinels and chromites from spectral analysis stems from the relationship between composition and petrogenetic conditions (pressure, temperature, oxygen fugacity) and the widespread presence of spinels and chromites in the inner solar system. When coupled with the ability to derive compositional information for mafic silicates from spectral analysis, this opens up the possibility of deriving petrogenetic information for remote spinel‐ and chromite‐bearing targets from analysis of their reflectance spectra.     

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.     

Determination of the Fe oxidation state of the Chassigny kaersutite: A microXANES spectroscopic study

Abstract— In order to elucidate the formation of low‐H kaersutites in Martian meteorites, the Fe³⁺/ΣFe ratio of Chassigny kaersutites in magmatic inclusions was directly determined by the synchrotron microXANES analysis. XANES analysis for standard kaersutites with known Fe³⁺/ΣFe ratios shows a linear relationship between centroid energy positions of XANES pre‐edge spectra and the Fe³⁺/ΣFe ratio. Based on the linear relationship, the Fe³⁺/ΣFe ratio of Chassigny kaersutites is estimated to be about 0.05. The low Fe³⁺/ΣFe ratio clearly suggests that low‐H kaersutites in Chassigny are not likely to be formed by the oxidation‐dehydrogenation reactions. The low‐H content of the Chassigny kaersutites is mainly due to the presence of a Ti oxy‐component.     

Spectral characterization of weathering products of elemental iron in a Martian atmosphere: Implications for Mars hyperspectral studies

Visible and near-infrared spectroscopic properties have been measured on elemental iron experimentally weathered in simulated Martian atmosphere and correlated to mineralogical compositions determined by X-ray diffraction. Two main features are observed in the reflectance spectra, corresponding to two deep bands located at 0.9 and 3.1 μm, respectively the iron band and the hydration band. In early weathering stages both Fe²⁺ and Fe³⁺ bands are identified. In addition, whereas the water band position does not change with time, the Fe²⁺ band disappears, and the Fe³⁺ band shifts towards longer wavelength (from 0.88 to 0.92 μm) because of transition from Fe²⁺ phases (siderite) to Fe³⁺ phases (ferrihydrite and goethite). Apart from these spectral signatures, other bands more specific of each phase are not clearly evidenced, especially for siderite. This is due to relatively low abundance of siderite (<20 wt%), but also to the very small grain size of secondary phase as well as surface coatings of iron (oxy)hydroxides. Therefore, our results suggest that carbonates, even if not detected, could be present in the form of very small grains in the surface of Mars.     

Asteroid 3628 Božněmcová: Covered with angrite‐like basalts?

Abstract— A detailed analysis of the reflectance spectrum of asteroid 3628 Bo?němcová, previously identified as a possible ordinary chondrite parent body, indicates that its surface consists of an assemblage dominated by clinopyroxene and plagioclase feldspar. The clinopyroxene is Fe²⁺‐bearing (likely in the range Fs_?10–20), with >90% of the Fe²⁺ being present in the M1 crystallographic site (spectral type A). The clinopyroxene:plagioclase feldspar ratio is between ?2 and 3 (?55–75% clinopyroxene, ?20–33% plagioclase feldspar). If olivine is present, the clinopyroxene:olivine ratio is >?3 (<20% olivine). The derived mineralogy of Bo?němcová is most similar, but not identical, to the known angrite meteorites. The data suggest that Bo?němcová formed by melting and differentiation of an oxidized chondritic precursor and probably represents an unsampled angrite‐like body.