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.     

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

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

Mercury surface composition: Integrating petrologic modeling and remote sensing data to place constraints on FeO abundance

A significant opaque component in Mercury’s crust is inferred based on albedo and spectral observations. Previous workers have favored iron-titanium bearing oxide minerals as the spectrally neutral opaque. A consequence of this hypothesis is that Mercury’s surface would have a high FeO content. An array of remote sensing techniques have not provided definitive constraints on the FeO content of Mercury’s surface. However, spectral observations have not detected a diagnostic 1 μm absorption band and have thus limited the FeO in coexisting silicates to <2 wt.% FeO. In this paper, we assess equilibrium among oxide and silicate minerals to constrain the distribution of iron between opaque oxides and silicates under a variety of environmental conditions. Equilibrium modeling is favored here because the geologic process that produced Mercury’s low-albedo intermediate terrain must have occurred globally, which favors a common widespread igneous process. Based on our modeling, we find that iron-rich ilmenite cannot occur with silicates that do not display a 1 μm absorption feature unless plagioclase abundances are high. However, such high plagioclase abundances are precluded by Mercury’s low albedo. Incorporating equilibrium crystallization modeling with spectral and albedo constraints we find the iron abundance of Mercury’s intermediate terrain is ?10 wt.% FeO. This intermediate iron composition matches constraints provided by visible albedo and total neutron absorption observed by MESSENGER. In fact, the total neutron absorption of mixtures of oxide, plagioclase, olivine and pyroxene for the oxide abundances estimated for Mercury, favor Mg-rich members of the ilmenite-geikielite solid-solution series. This work offers compositional constraints for Fe, Ti, and Mg that will be testable by various MESSENGER instrument data sets after it begins its orbital mission.     

Spectral reflectance properties of carbonaceous chondrites: 2. CM chondrites

We have examined the spectral reflectance properties and available modal mineralogies of 39 CM carbonaceous chondrites to determine their range of spectral variability and to diagnose their spectral features. We have also reviewed the published literature on CM mineralogy and subclassification, surveyed the published spectral literature and added new measurements of CM chondrites and relevant end members and mineral mixtures, and measured 11 parameters and searched pair-wise for correlations between all quantities. CM spectra are characterized by overall slopes that can range from modestly blue-sloped to red-sloped, with brighter spectra being generally more red-sloped. Spectral slopes, as measured by the 2.4:0.56 μm and 2.4 μm:visible region peak reflectance ratios, range from 0.90 to 2.32, and 0.81 to 2.24, respectively, with values <1 indicating blue-sloped spectra. Matrix-enriched CM spectra can be even more blue-sloped than bulk samples, with ratios as low as 0.85. There is no apparent correlation between spectral slope and grain size for CM chondrite spectra - both fine-grained powders and chips can exhibit blue-sloped spectra. Maximum reflectance across the 0.3-2.5 μm interval ranges from 2.9% to 20.0%, and from 2.8% to 14.0% at 0.56 μm. Matrix-enriched CM spectra can be darker than bulk samples, with maximum reflectance as low as 2.1%. CM spectra exhibit nearly ubiquitous absorption bands near 0.7, 0.9, and 1.1 μm, with depths up to 12%, and, less commonly, absorption bands in other wavelength regions (e.g., 0.4-0.5, 0.65, 2.2 μm). The depths of the 0.7, 0.9, and 1.1 μm absorption features vary largely in tandem, suggesting a single cause, specifically serpentine-group phyllosilicates. The generally high Fe content, high phyllosilicate abundance relative to mafic silicates, and dual Fe valence state in CM phyllosilicates, all suggest that the phyllosilicates will exhibit strong absorption bands in the 0.7 μm region (due to Fe³⁺-Fe²⁺ charge transfers), and the 0.9-1.2 μm region (due to Fe²⁺ crystal field transitions), and generally dominate over mafic silicates. CM petrologic subtypes exhibit a positive correlation between degree of aqueous alteration and depth of the 0.7 μm absorption band. This is consistent with the decrease in fine-grained opaques that accompanies aqueous alteration. There is no consistent relationship between degree of aqueous alteration and evidence for a 0.65 μm region saponite-group phyllosilicate absorption band. Spectra of different subsamples of a single CM can show large variations in absolute reflectance and overall slope. This is probably due to petrologic variations that likely exist within a single CM chondrite, as duplicate spectra for a single subsample show much less spectral variability. When the full suite of available CM spectra is considered, few clear spectral-compositional trends emerge. This indicates that multiple compositional and physical factors affect absolute reflectance, absorption band depths, and absorption band wavelength positions. Asteroids with reflectance spectra that exhibit absorption features consistent with CM spectra (i.e., absorption bands near 0.7 and 0.9 μm) include members from multiple taxonomic groups. This suggests that on CM parent bodies, aqueous alteration resulted in the consistent production of serpentine-group phyllosilicates, however resulting absolute reflectances and spectral shapes seen in CM reflectance spectra are highly variable, accounting for the presence of phyllosilicate features in reflectance spectra of asteroids across diverse taxonomic groups.     

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).     

Spectral properties of plagioclase and pyroxene mixtures and the interpretation of lunar soil spectra

The effects of particle size and mineral proportions on the spectral characteristics of plagioclase and pyroxene mixtures are investigated. Size separates (<25 μm, 25–45 μm, 45–75 μm, 75–125 μm, 125–250 μm, and 250–500 μm) have been prepared for the following labradorite/enstatite compositional mixtures: 100/0%, 95/5%, 85/15%, 50/50%, and 0/100%. Spectrally, the labradorite and enstatite samples are representative of the plagioclase feldspars and the orthopyroxenes: the labradorite exhibits a weak, broadband centered near 1.25 μm and the enstatite exhibits two well-defined bands centered near 0.9 and 1.9 μm. From analysis of the plagioclase bands of the mixtures, it is found that (1) the amount of plagioclase necessary for the plagioclase band to be observed as a discrete absorption band is dependent on particle size and (2) plagioclase can be detected by flattening of the pyroxene reflectance “peak” between the 0.9- and 1.9-μm absorption bands if significant amounts of plagioclase are present. Analogs for immature and mature lunar highland soils have been created to examine the combined effects of particle size and mineral proportions on spectra of plagioclase and pyroxene mixtures. bidirectional reflectance spectra of these soil analogs are used to examine the detectability of plagioclase in soil-like particle size distributions. Plagioclase in significant amounts is detected by the flattening of the pyroxene reflectance “peak” between the 0.9- and 1.9-μm absorption bands, and the plagioclase absorption band itself is observed with 85% plagioclase present. The soil analogs reveal that particle size accounts for only a minor spectral difference between immature and mature lunar highland soils. From comparisons with spectra of returned lunar samples, agglutinates are found to dominate the spectral variations associated with soil maturity. Spectra of the immature soil analogs can be used to estimate the minimum pyroxene abundance for immature regions observed remotely.     

On the presence of phyllosilicate minerals in the interstellar grains

The composition of the interstellar silicate dust is investigated. Condensation or alteration of silicate grains at temperatures of a few hundred degrees, in the presence of H₂O, would result in hydrous or phyllosilicates, the silicate type most abundant in the type I carbonaceous chondrites. Infrared spectra of small particles (～0.1 μ) of the high temperature condensates, olivine and pyroxene, at 300 K and 4 K do not give a good match to the interstellar absorption band near 9.8 μ. Laboratory spectra of several phyllosilicates give better agreement as does the spectrum of a carbonaceous chondrite. We propose that the silicates in the interstellar grains are predominantly phyllosilicates and suggest additional spectral tests for this hypothesis.     

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.     

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.     

Mineralogical interpretation of reflectance spectra of Eros from NEAR near‐infrared spectrometer low phase flyby

Abstract— High signal‐to‐noise near‐infrared spectrometer (NIS) spectra acquired during the low phase flyby of the near‐Earth asteroid rendezvous (NEAR) mission to 433 Eros are analyzed to determine mineral chemistry and proportions of mafic silicates across the asteroid's surface at 2.68 × 5.50 km spatial resolution. Spectral band parameters are derived, and compared with those of laboratory samples of known mineral composition, grain size distribution and terrestrial, meteoritic and lunar pyroxene spectral properties. The NIS derived band parameters are consistent with ordinary chondrite meteorites. We invoke the presence of a clinopyroxene component in the spectra, which is consistent with ordinary chondrite mineralogy and/or some degree of partial melting of ordinary chondritic material. Spectra measured across the surface of Eros can reveal small but real spectral variations. Most relative spectra are uniform to within 1–2%. Some areas suggest compositional variations of a few percent. Spectral slope variations of a few percent are seen indicating a non‐uniform distribution of materials affecting the slope parameter but with no resolved absorption bands. We find no correlation of slope with viewing geometry or compositional variation. The band parameter values do not consistently indicate a specific ordinary chondrite class but Eros is definitely undifferentiated with possible compositional variations of no more than 1–2%.     

Spectral reflectance properties of carbonaceous chondrites: 3. CR chondrites

Powdered samples of a suite of 14 CR and CR-like chondrites, ranging from petrologic grade 1 to 3, were spectrally characterized over the 0.3–2.5 μm interval as part of a larger study of carbonaceous chondrite reflectance spectra. Spectral analysis was complicated by absorption bands due to Fe oxyhydroxides near 0.9 μm, resulting from terrestrial weathering. This absorption feature masks expected absorption bands due to constituent silicates in this region. In spite of this interference, most of the CR spectra exhibit absorption bands attributable to silicates, in particular an absorption feature due to Fe²⁺-bearing phyllosilicates near 1.1 μm. Mafic silicate absorption bands are weak to nonexistent due to a number of factors, including low Fe content, low degree of silicate crystallinity in some cases, and presence of fine-grained, finely dispersed opaques. With increasing aqueous alteration, phyllosilicate: mafic silicate ratios increase, resulting in more resolvable phyllosilicate absorption bands in the 1.1 μm region. In the most phyllosilicate-rich CR chondrite, GRO 95577 (CR1), an additional possible phyllosilicate absorption band is seen at 2.38 μm. In contrast to CM spectra, CR spectra generally do not exhibit an absorption band in the 0.65–0.7 μm region, which is attributable to Fe³⁺–Fe²⁺ charge transfers, suggesting that CR phyllosilicates are not as Fe³⁺-rich as CM phyllosilicates. CR2 and CR3 spectra are uniformly red-sloped, likely due to the presence of abundant Fe–Ni metal. Absolute reflectance seems to decrease with increasing degree of aqueous alteration, perhaps due to the formation of fine-grained opaques from pre-existing metal. Overall, CR spectra are characterized by widely varying reflectance (4–21% maximum reflectance), weak silicate absorption bands in the 0.9–1.3 μm region, overall red slopes, and the lack of an Fe³⁺–Fe²⁺ charge transfer absorption band in the 0.65–0.7 μm region.     

Multiple emission angle surface-atmosphere separations of thermal emission spectrometer data

A method for separating the spectral signatures of the Martian surface and atmosphere was developed and is applied to multiple emission angle data returned from the MGS TES instrument. This method includes correlated-k and index gas removal algorithms that may be applied to all nadir-pointing TES data. Initial results have provided new and refined measurements of the spectral shapes of atmospheric dust and the Martian surface. Surface temperatures and atmospheric dust opacities are also retrieved with improved accuracy over single observation temperature and opacity retrievals. Low-albedo surfaces display absorptions consistent in both shape and depth with previous studies. These surfaces may be closely modeled using a combination of previously derived basalt, andesitic, and high-albedo surface spectral shapes. Short wavelengths display no significant absorptions, indicating both the coarse particulate nature of the surface and the lack of significant amounts of carbonate. Moderate- and high-albedo surfaces have spectral shapes distinctive of fine particulate silicate materials. No single material can match the entire high-albedo surface spectrum, though there are clear indications of a material that closely matches intermediate to calcic plagioclase and an emission peak at ∼1620 cm⁻¹ due to bound water. The lack of residual restrahlen silicate absorptions indicates that minerals such as olivine or pyroxene are not present in high-albedo surfaces at significant (but unknown) abundances. High-albedo surface results presented here are in agreement with and complementary to shorter wavelength observations. The Martian dust is composed of both primary and secondary minerals. Either chemical weathering has not completely altered its source material or the soil is a mixture of altered and unaltered sources. Further laboratory studies are needed to better establish detection limits and behavior of mineral mixtures of fine particulates in the thermal infrared portion of the spectrum.     

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.     

Optical characterization of laser ablated silicates

We perform an optical characterization of UV laser ablated silicates (olivine, pyroxene), starting from their reflectance spectra in the 0.3-2.5 μm spectral range. The goal is to provide useful tools to model space weathering effects on surfaces of asteroids and TNOs (trans-neptunian objects). We determine that the reddening and darkening spectral trend is compatible with the Hapke's space weathering model, using the optical constants of metallic iron in a silicate matrix. This result is supported by new magnetic susceptibility measurements on laser ablated orthopyroxene. We also investigate the potential contribution of formation of amorphous silicates in the process. Applying our results to silicate-rich surfaces in the Solar System, we investigate the possibility of a weathered olivine component on the surface of Centaur 5145 Pholus. Inclusion of this component slightly decreases the amount of complex organics and water ice from those previously estimated. Thus, the current Pholus spectrum is consistent with the presence of either unweathered or weathered olivine, or potentially both materials.     

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.     

The composition and size distribution of the dust in the coma of Comet Hale-Bopp

We discuss the composition and size distribution of the dust in the coma of Comet Hale-Bopp. We do this using a model fit for the infrared emission measured by the Infrared Space Observatory (ISO) and the measured degree of linear polarization of scattered light at various phase angles and wavelengths. The effects of particle shape on the modeled optical properties of the dust grains are taken into account. Both the short wavelength (7-44 μm) and the long wavelength (44-120 μm) infrared spectrum are fitted using the same dust parameters, as well as the degree of linear polarization at twelve different wavelengths in the optical to near-infrared domains. We constrain our fit by forcing the abundances of the major rock forming chemical elements to be equal to those observed in meteorites. The infrared spectrum at long wavelengths reveals that large grains are needed in order to fit the spectral slope. The size and shape distribution we employ allows us to estimate the sizes of the crystalline silicates. The ratios of the strength of various forsterite features show that the crystalline silicate grains in Hale-Bopp must be submicrometer-sized. On the basis of our analysis the presence of large crystalline silicate grains in the coma can be excluded. Because of this lack of large crystalline grains combined with the fact that we do need large amorphous grains to fit the emission spectrum at long wavelengths, we need only approximately 4% of crystalline silicates by mass (forsterite and enstatite) to reproduce the observed spectral features. After correcting for possible hidden crystalline material included in large amorphous grains, our best estimate of the total mass fraction of crystalline material is ∼7.5%, which is significantly lower than deduced in previous studies in which the typical derived crystallinity is ∼20-30%. The implications of this low abundance of crystalline material on the possible origin and evolution of the comet are discussed. We conclude that the crystallinity we observe in Hale-Bopp is consistent with the production of crystalline silicates in the inner Solar System by thermal annealing and subsequent radial mixing to the comet forming region (∼30 AU).     

Estimating the modal mineralogy of eucrite and diogenite meteorites using visible–near infrared reflectance spectroscopy

Reliable quantitative mapping of minerals exposed on Vesta's surface is crucial for understanding the crustal composition, petrologic evolution, and surface modification of the howardite, eucrite, and diogenite (HED) parent body. However, mineral abundance estimates derived from visible–near infrared (VIS–NIR) reflectance spectra are complicated by multiple scattering, particle size, and nonlinear mixing effects. Radiative transfer models can be employed to accommodate these issues, and here we assess the utility of such models to accurately and efficiently determine modal mineralogy for a suite of eucrite and olivine‐bearing (harzburgitic) diogenite meteorites. Hapke and Shkuratov radiative transfer models were implemented to simultaneously estimate mineral abundances and particle size from VIS–NIR reflectance spectra of these samples. The models were tested and compared for laboratory‐made binary (pyroxene–plagioclase) and ternary mixtures (pyroxene–olivine–plagioclase) as well as eucrite and diogenite meteorite samples. Results for both models show that the derived mineral abundances are commonly within 5–10% of modal values and the estimated particle sizes are within the expected ranges. Results for the Hapke model suggest a lower detection limit for olivine in HEDs when compared with the Shkuratov model (5% versus 15%). Our current implementation yields lower uncertainties in mineral abundance (commonly <5%) for the Hapke model, though both models have an advantage over typically used parameters such as band depth, position, and shape in that they provide quantitative information on mineral abundance and particle size. These results indicate that both the Hapke and Shkuratov models may be applied to Dawn VIR data in a computationally efficient manner to quantify the spatial distribution of pyroxene, plagioclase, and olivine on the surface of Vesta.     

Mineralogy of the lunar crust: Results from Clementine

Abstract— The central peaks of 109 impact craters across the Moon are examined with Clementine ultraviolet-visible (UVVIS) camera multispectral data. The craters range in diameter from 40 to 180 km and are believed to have exhumed material from 5–30 km beneath the surface to form the peaks, including both upper and lower crustal rocks depending on whether craters have impacted into highlands or basins. Representative five-color spectra from spectrally and spatially distinct areas within the peaks are classified using spectral parameters, including “key ratio” (which is related to mafic mineral abundance) and “spectral curvature” (linked to absorption band shape, which distinguishes between low- and high-Ca pyroxene and olivine). The spectral parameters are correlated to mineralogical abundances, related in turn to highland plutonic rock compositions. The derived rock compositions for the various central peaks are presented in a global map. From these results, it is evident that the lunar crust is compositionally diverse, both globally and at local 100 m scales found within individual sets of central peaks. Although the central peaks compositions imply a crust that is generally consistent with previous models of crustal structure, they also indicate a more anorthositic crust than generally assumed, with a bulk plagioclase content of ～81%, evolving from “pure” anorthosite near the surface towards more mafic, low-Ca pyroxene-rich compositions with depth (comparable to anorthositic norite). Evidence for mafic plutons occurs in both highlands and basins and represent all mafic highland rock types. However, the lower crust is more compositionally diverse than the highlands, with both a greater range of rock types and more diversity within individual sets of central peaks.     

Lithological mapping of central part of Mare Moscoviense using Chandrayaan-1 Hyperspectral Imager (HySI) data

We conducted spectral analysis of central region of the Mare Moscoviense area on the far side of the Moon using the Hyperspectral Imager (HySI) data from the Chandrayaan-1 mission in an effort to identify and map the major lithological units present in the area. Various spectral band parameters, namely, band curvature, band tilt and band strength have been used for lithological discrimination based on the nature of the spectral profile. These band parameters essentially measure the shape, position and strength of the absorption feature near 1000 nm arising due to electronic transition of Fe²⁺ in crystallographic sites of major rock forming silicates. Spectral band parameters have been used for generating rock type composite image. Based on spectral studies and rock type composite image as obtained using band parameters, five major compositional units have been identified: highland basin soils, ancient mature mare, highland contaminated mare, buried unit with abundant low-Ca pyroxene (LCP), and youngest mare unit. In the present study, a multispectral approach in the form of spectral band parameters has been adopted for analysing the HySI hyperspectral data from Chandrayaan-1 mission. Present study clearly shows that the spectral band parameters obtained using selected HySI channels could efficiently be used to discriminate and delineate the major litho-units present across the central part of Mare Moscoviense and the same approach can thus be used for lithological mapping of other parts of lunar surface using HySI data.     

Genesis of the IIICD iron meteorites: Evidence from silicate-bearing inclusions

Abstract— Our studies of the silicate-bearing inclusions in the IIICD iron meteorites Maltahöhe, Carlton and Dayton suggest that their mineralogy and mineral compositions are related to the composition of the metal in the host meteorites. An inclusion in the low-Ni Maltahöhe is similar in mineralogy to those in IAB irons, which contain olivine, pyroxene, plagioclase, graphite and troilite. With increasing Ni concentration of the metal, silicate inclusions become poorer in graphite, richer in phosphates, and the phosphate and silicate assemblages become more complex. Dayton contains pyroxene, plagioclase, SiO₂, brianite, panethite and whitlockite, without graphite. In addition, mafic silicates become more FeO-rich with increasing Ni concentration of the hosts. In contrast, silicates in IAB irons show no such correlation with host Ni concentration, nor do they have the complex mineral assemblages of Dayton. These trends in inclusion composition and mineralogy in IIICD iron meteorites have been established by reactions between the S-rich metallic magma and the silicates, but the physical setting is uncertain. Of the two processes invoked by other authors to account for groups IAB and IIICD, fractional crystallization of S-rich cores and impact generation of melt pools, we prefer core crystallization. However, the absence of relationships between silicate inclusion mineralogy and metal compositions among IAB irons analogous to those that we have discovered in IIICD irons suggests that the IAB and IIICD cores/metallic magmas evolved in rather different ways. We suggest that the solidification of the IIICD core may have been very complex, involving fractional crystallization, nucleation effects and, possibly, liquid immiscibility.