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.     

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.     

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.     

Near-infrared reflectance spectroscopy of Ca-rich clinopyroxenes and prospects for remote spectral characterization of planetary surfaces

We present results of laboratory near-infrared reflectance studies of a set of calcic pyroxenes with comparable calcium contents (Wo_45-50) but variable iron content and oxidation states. This new dataset complements earlier published data (Cloutis and Gaffey, 1991, J. Geophys. Res. 96, 22809-28826, and references therein). In particular, our new spectra extend the scarce available spectral data on chemically analyzed Fe-rich high-Ca clinopyroxenes. We attempted to interpret the spectral behavior of our samples in terms of chemistry and coordination site occupancies. Tentatively, we conclude that Fe-rich calcic pyroxenes have very low contents of Fe²⁺ in the M2 sites and belong to the spectral type A lacking the 2-μm band. This may be due to high Ca and Mn contents in these pyroxenes. Fe-poor high-Ca pyroxenes are more spectrally variable. In general, they tend to belong to the spectral type B with two major bands near 1 and 2 μm, unless the samples have high Fe³⁺/Fe²⁺ ratios or are rich in Mn and Ca. Some of them (including unusual meteorite Angra dos Reis) are of type B despite very high Ca contents. We applied the Modified Gaussian Model (MGM) to characterize three major Fe²⁺ absorption bands in the 1-μm region of the spectra of Ca-rich pyroxenes. Only the band due to Fe²⁺ in the M1 coordination site near 1.15 μm may be potentially useful to estimate the Fe content in calcic pyroxenes on remotely-sensed surfaces of Solar System bodies. The spectral variability of basaltic meteorites (angrites) that are rich in calcic pyroxenes is also discussed. The presence of spectral type A calcic pyroxenes in these meteorites complicates unambiguous identification of olivine in asteroid spectra.     

High‐albedo asteroid 434 Hungaria: Spectrum,composition and genetic connections

Abstract— New data in the wavelength region of approximately 0.4–2.5 μm have been obtained for asteroid 434 Hungaria. This is the most complete visible to near‐infrared spectrum to date for this object. The near‐infrared portion of the spectrum (about 0.8–2.5 μm) is smooth, featureless, and agrees well in the overlap region with new visible region data. However, visible region (about 0.45–0.9 μm) data appear to exhibit weak, broad spectral absorption features near 0.5, 0.6–0.7, and 1 μm. If real, the presence of such features would strongly constrain the compositional determination of Hungaria since it has a relatively high albedo of 46%. Most minerals that exhibit similar absorption features, and are commonly found in meteorites, have a much lower albedo. Asteroid 434 Hungaria has been observed more than six times in these overlapping spectral regions, and it is now possible to assess its mineral composition with some confidence. The dominant phase on this asteroid is an iron‐free mineral, probably enstatite. Hungaria may contain secondary phases causing subtle, visible‐region absorption features. Alternatively, the surface layer(s) of the asteroid may be contaminated by an absorbing species from an external source.     

FTIR 2–16 micron spectroscopy of micron‐sized olivines from primitive meteorites

Abstract— Infrared spectra of mineral grains from primitive meteorites could be useful for comparison with astronomical infrared spectra since some of their grains might be similar to those formed in the planet‐forming disks around young stars or in the envelopes surrounding late‐type stars. To assess the usefulness of meteorite spectra, olivine grains separated from primitive meteorites have been analyzed using FTIR microscope techniques in the 2–16 μm wavelength range. The sub‐micron sizes of the grains made a complex preparation process necessary. Five characteristic bands were measured near 11.9, 11.2, 10.4, 10.1, and 10.0 μm. The results of 59 analyses allow the calculation of band positions for meteoritic olivines as a function of their iron and magnesium contents. Comparison of the meteoritic results with astronomical data for comets and dust around young and old stars, which exhibit bands similar to the strongest infrared bands observed in the grains (at 11.2 μm), show that the spectral resolution of the astronomical observations is too low to ascertain the exact iron and magnesium (Mg: Fe) ratio of the dust in the 8–13 μm wavelength range.     

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.     

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.     

Visible–near infrared spectral indices for mapping mineralogy and chemistry with OSIRIS‐REx

The primary objective of the Origins, Spectral Interpretation, Resource Identification, and Security–Regolith Explorer (OSIRIS‐REx) mission is to return to Earth a pristine sample of carbonaceous material from the primitive asteroid (101955) Bennu. To support compositional mapping of Bennu as part of sample site selection and characterization, we tested 95 spectral indices on visible to near infrared laboratory reflectance data from minerals and carbonaceous meteorites. Our aim was to determine which indices reliably identify spectral features of interest. Most spectral indices had high positive detection rates when applied to spectra of pure, single‐component materials. The meteorite spectra have fewer and weaker absorption features and, as a result, fewer detections with the spectral indices. Indices targeting absorptions at 0.7 and 2.7–3 μm, which are attributable to hydrated minerals, were most successful for the meteorites. Based on these results, we identified a set of 17 indices that are most likely to be useful at Bennu. These indices detect olivines, pyroxenes, carbonates, water/OH‐bearing minerals, serpentines, ferric minerals, and organics. Particle size and albedo are known to affect band depth but had a negligible impact on interpretive success with spectral indices. Preliminary analysis of the disk‐integrated Bennu spectrum with these indices is consistent with expectations given the observed absorption near 3 μm. Our study prioritizes spectral indices to be used for OSIRIS‐REx spectral analysis and mapping and informs the reliability of all index‐derived data products, including a science value map for sample site selection.     

Vesta: The first pyroxene band from new spectroscopic measurements

New spectral reflectance measurements of asteroid 4 Vesta were obtained using a silicon vidicon spectrometer with a resolution of 0.002–0.004 μm. The major absorption band in the near infrared has a minimum at 0.924 ± 0.004 μm with a bandwidth of 0.18 μm full width at half power (fwhp). The band represents a 30% absorption relative to peak reflectance at 0.75 μm. The absorption band has been interpreted to be due to electronic absorptions in ferrous iron in sixfold coordination in the pyroxene, pigeonite. The increased spectral resolution of these observations compared to earlier spectrophotometry enables us to refine the pyroxene composition, from the position of the Fe²⁺ absorption band, and arrive at a relative calcium content [Ca/(Mg + Fe + Ca)] of 10–12%. The absorption band is symmetric about its center, implying the presence of little or no olivine. The existence of the 2.0-μm pyroxene band which was verified by Larson and Fink (1975) confirms the interpretation based on the 1.0-μm band.     

MUSES‐C target asteroid (25143) 1998 SF36: A reddened ordinary chondrite

Abstract— Near‐Earth asteroid (25143) 1998 SF36 is a planned target for the Japanese MUSES‐C sample return mission. High signal‐to‐noise and relatively high‐resolution (50 Å) visible and near‐infrared spectroscopic measurements obtained during this asteroid's favorable 2001 apparition reveal it to have a red‐sloped S(IV)‐type spectrum with strong 1 and 2 μm absorption bands analogous to those measured for ordinary chondrite meteorites. This red slope, which is the primary spectral difference between (25143) 1998 SF36 and ordinary chondrite meteorites, is well modeled by the spectrum of 0.05% nanophase iron (npFe⁰) proposed as a weathering mechanism by Pieters et al. (2000). Asteroid 1998 SF36 appears to have a surface composition corresponding to that of ordinary chondrite meteorites and is most similar in spectral characteristics and modeled olivine/pyroxene content to the LL chondrite class.     

Importance of space weathering simulation products in compositional modeling of asteroids: 349 Dembowska and 446 Aeternitas as examples

Abstract— Based on recent progress in simulating space weathering on asteroids using pulse‐laser irradiation onto olivine and orthopyroxene samples, detailed analyses of two of the A and R type asteroid reflectance spectra have been performed using reflectance spectra of laser‐treated samples. The visible‐near‐infrared spectrum of olivine is more altered than that of pyroxene at the same pulse‐laser energy, suggesting that olivine weathers more rapidly than orthopyroxene in space. The same trend can be detected from reflectance spectra of the asteroids, where the more olivine an asteroid has, the redder its 1 μm band continuum can become. Comparison of the 1 μm band continuum slope and the 2/1 μm band area ratio between the asteroids and olivine and pyroxene samples (including the laser‐treated ones) suggests that asteroids may be limited in the degree of space weathering they can exhibit, possibly due to the short life of their surface regolith. Their pyroxenes may also have a limited chemical composition range. Fitting the visible continuum shape and other parts of the spectra (especially the 2μm part) has been impossible with any combination of common rock‐forming minerals such as silicates and metallic irons. However, this study shows, for the first time, excellent fits of reflectance spectra of an A asteroid (Aeternitas) and an R asteroid (Dembowska), including their visible spectral curves, band depths and shapes, and overall continuum shapes. Our results provide estimates that Aeternitas consists of 2% fresh olivine, 93% space‐weathered olivine, 1% space‐weathered orthopyroxene, and 4% chromite, and that Dembowska consists of 1% fresh olivine, 55% space‐weathered olivine, and 44% space‐weathered orthopyroxene. These results suggest that space weathering effects maybe important to the interpretation of asteroid reflectance spectra, even those with deep silicate absorption bands. Modified Gaussian model deconvolutions of the laser‐irradiated olivine samples show that their identity as olivine remained. The most recent submicroscopic mineralogical analyses have revealed that the laser‐irradiated olivine samples contain nanophase iron particles similar to those in space‐weathered lunar samples.     

Complexities in pyroxene compositions derived from absorption band centers: Examples from Apollo samples,HED meteorites,synthetic pure pyroxenes,and remote sensing data

We reexamine the relationship between pyroxene composition and near‐infrared absorption bands, integrating measurements of diverse natural and synthetic samples. We test an algorithm (PLC) involving a two‐part linear continuum removal and parabolic fits to the 1 and 2 μm bands—a computationally simple approach which can easily be automated and applied to remote sensing data. Employing a suite of synthetic pure pyroxenes, the PLC technique is shown to derive similar band centers to the modified Gaussian model. PLC analyses are extended to natural pyroxene‐bearing materials, including (1) bulk lunar basalts and pyroxene separates, (2) diverse lunar soils, and (3) HED meteorites. For natural pyroxenes, the relationship between composition and absorption band center differs from that of synthetic pyroxenes. These differences arise from complexities inherent in natural materials such as exsolution, zoning, mixing, and space weathering. For these reasons, band center measurements of natural pyroxene‐bearing materials are compositionally nonunique and could represent three distinct scenarios (1) pyroxene with a narrow compositional range, (2) complexly zoned pyroxene grains, or (3) a mixture of multiple pyroxene (or nonpyroxene) components. Therefore, a universal quantitative relationship between band centers and pyroxene composition cannot be uniquely derived for natural pyroxene‐bearing materials without additional geologic context. Nevertheless, useful relative relationships between composition and band center persist in most cases. These relationships are used to interpret M³ data from the Humboldtianum Basin. Four distinct compositional units are identified (1) Mare Humboldtianum basalts, (2) distinct outer basalts, (3) low‐Ca pyroxene‐bearing materials, and (4) feldspathic materials.     

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.     

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.     

Spectral properties of angrites

Abstract— Angrites are generally believed to be fragments of a basaltic asteroid that differentiated under relatively oxidizing conditions. Almost all angrites (e.g., D'Orbigny, Lewis Cliff [LEW] 86010, and Sahara 99555) are composed predominately of anorthite, Al‐Ti diopside‐hedenbergite, and Ca‐rich olivine, except for the type specimen, Angra dos Reis, which is composed almost entirely of Al‐Ti diopside‐hedenbergite. D'Orbigny, LEW 86010, and Sahara 99555 also have spectral properties very different from Angra dos Reis. These newly measured angrites all have broad absorption features centered near 1 μm with very weak to absent absorption bands at ?2 μm, which is characteristic of some clinopyroxenes. The spectrum of Angra dos Reis has the characteristic 1 and 2 μm features due to pyroxene. One asteroid, 3819 Robinson, has similar spectral properties to the newly measured angrites in the visible wavelength region, but does not appear to spectrally match these angrites in the near‐infrared.     

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.     

Ground-based near infrared spectroscopy of Jupiter's ring and moons

The backscattered reflectivity of Jupiter's ring has been previously measured over distinct visible and near infrared wavelength bands by a number of ground-based and spaceborne instruments. We present spectra of Jupiter's main ring from 2.21-2.46 μm taken with the NIRSPEC spectrometer at the W.M. Keck observatory. At these wavelengths, scattered light from Jupiter is minimal due to the strong absorption of methane in the planet's atmosphere. We find an overall flat spectral slope over this wavelength interval, except for a possible red slope shortward of 2.25 μm. We extended the spectral coverage of the ring to shorter wavelengths by adding a narrow-band image at 1.64 μm, and show results from 2.27-μm images over phase angles of 1.2°-11.0°. Our images at 1.64 and 2.27 μm reveal that the halo contribution is stronger at the shorter wavelength, possibly due to the redder spectrum of the ring parent bodies as compared with the halo dust component. We find no variation in main ring reflectivity over the 1.2°-11.0° phase angle range at 2.27 μm. We use adaptive optics imaging at the longer wavelength L′ band (3.4-4.1 μm) to determine a 2-σ upper limit of 22 m of vertically-integrated I/F. Our observing campaign also produced an L′ image of Callisto, showing a darker leading hemisphere, and a spectrum of Amalthea over the 2.2-2.5 and 2.85-3.03 μm ranges, showing deep 3-μm absorption.     

Vestoid surface composition from analysis of faint absorption bands in visible reflectance spectra

Faint absorption bands in the visible range of the smoothed vestoid spectra have been found. The bands centered near 505, 530, and 550 nm are attributed to ferrous iron in low-calcium pyroxene and are typical for pyroxene-bearing vestoid surfaces. In accordance with characteristics of the faint absorption bands around 600 and 650 nm the studied vestoid spectra can be sorted into five types. Since the same absorptions are also seen in the laboratory spectra of the minerals and meteorites, which appear to be similar to vestoid material, spectral types of the vestoids can be related to their surface compositions. Regolith of the Type-I vestoids consists of pure low-calcium pyroxenes. Minor amount of olivine along with pyroxene appear to be on the Type-II vestoids whereas the mixtures of low-calcium pyroxene with minor chromite define the Type-III and -IV. The causes for the fifth spectral type in terms of minor mineral phases are unclear now. Simulation of the spectra of vestoids was employed to estimate content of olivine (∼6-12 vol%) and chromite (∼12-30 vol%) on their surfaces.     

Synchrotron‐based infrared microspectroscopy as a useful tool to study hydration states of meteorite constituents

Abstract— We present the results of the infrared (IR) microscopic study of the anomalous carbonaceous chondrites Dhofar (Dho) 225 and Dhofar 735 in comparison to typical CM2 chondrites Cold Bokkeveld, Murray, and Mighei. The Fourier transform infrared (FTIR) 2.5–14 μm reflectance measurements were performed on conventional polished sections using an infrared microscope with a synchrotron radiation source. We demonstrate that the synchrotron‐based IR microspectroscopy is a useful, nondestructive tool for studying hydration states of meteorite constituents in situ. Our results show that the matrices of Dho 225 and Dho 735 are dehydrated compared to the matrices of typical CM2 chondrites. The spectra of the Dho 225 and Dho 735 matrices lack the 2.7–2.8 μm absorption feature present in the spectra of Cold Bokkeveld, Murray, and Mighei. Spectral signatures caused by Si‐O vibrations in fine‐grained, Fe‐rich olivines dominate the 10 μm spectral region in the spectra of Dho 225 and Dho 735 matrices, while the spectra of normal CM2 chondrites are dominated by spectral signatures due to Si‐O vibrations in phyllosilicates. We did not detect any hydrated phases in the spectra of Dho 225 and Dho 735 polished sections. In addition, the near‐infrared reflectance spectra of Dho 225 and Dho 735 bulk powders show spectral similarities to the Antarctic metamorphosed carbonaceous chondrites. We confirm the results of previous mineralogical, chemical, and isotopic studies indicating that the two meteorites from Oman are the first non‐Antarctic metamorphosed carbonaceous chondrites.