Near-infrared spectroscopy of probable impact melt from three large lunar highland craters

The composition of small areas within three large lunar highland craters are compared using near-infrared, Earth-based telescopic data. Spectra from many areas in the walls and central peaks of the craters indicate the presence of crystalline components which include olivine, two types of pyroxene, and sometimes Fe-bearing feldspar. Spectra from other regions suspected of being impact melt deposits, located on the floors and walls of the three craters, have remarkably similar, yet anomalous features. These features are interpreted to indicate the presence of pyroxene, Fe-bearing glass, and Fe-bearing feldspar. Pyroxene and feldspar are believed to occur primarily in the form of lithic clasts and rapidly recrystallized impact melt. The Fe-bearing glass is interpreted as impact melt glass.     

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.     

Vestan lithologies mapped by the visual and infrared spectrometer on Dawn

We present global lithological maps of the Vestan surface based on Dawn mission's Visible InfraRed (VIR) Spectrometer acquisitions with a spatial sampling of 200 m. The maps confirm the results obtained with the data set acquired by VIR with a spatial sampling of 700 m, that the reflectance spectra of Vesta's surface are dominated by pyroxene absorptions that can be interpreted within the context of the distribution of howardites, eucrites, and diogenites (HEDs). The maps also partially agree with the ground and Hubble Space Telescope observations: they confirm the background surface being an assemblage of howardite or polymict eucrite, as well as the location of a diogenitic‐rich spot; however, there is no evidence of extended olivine‐rich regions in the equatorial latitudes. Diogenite is revealed on the Rheasilvia basin floor, indicating that material of the lower crust/mantle was exposed. VIR also detected diogenites along the scarp of Matronalia Rupes, and the rims of Severina and a nearby, unnamed crater, and as ejecta of Antonia crater. The diogenite distribution is fully consistent with petrological constraints; although the mapped distribution does not provide unambiguous constraints, it favors the hypothesis of a magma ocean.     

Dawn completes its mission at 4 Vesta

The Dawn mission was designed to test our hypothesis about the origin and evolution of the early solar system by visiting the largest differentiated basaltic asteroid, 4 Vesta, believed to be a survivor from the earliest times of rocky body formation. Observations from orbit show that Vesta is the parent body of the Howardite, Eucrite, Diogenite meteorites. Vesta has an iron core and a eucritic–diogenitic crust. Its surface is characterized by abundant impact craters but with no evident volcanic features. It has two ancient impact basins in the southern hemisphere that are associated with circum‐planetary troughs. The northern hemisphere is the more heavily cratered and contains the oldest terrains. The surface of Vesta is diverse, with north‐south and east‐west dichotomies in the eucrite‐to‐diogenite ratio. Its surface contains both very bright and very dark material, and its color varies strongly from region to region. Both the mineralogical and the elemental compositions agree with that expected for the HED parent body. Significant OH or H may be present in the upper crust and the presence of pits in “fresh” craters is consistent with the devolatilization of the surface after a collision either brought to or tapped a source of water on Vesta. The presence of dark material on the surface of Vesta suggests efficient transport pathways for organic material, and the mixing of the dark material with the more pristine pyroxene explains the varying albedo across the surface. Vesta has proven to be a reliable witness to the formation of the solar system.     

Thermal metamorphism of the C,G, B,and F asteroids seen from the 0.7 μm, 3 μm,and UV absorption strengths in comparison with carbonaceous chondrites

Abstract Thermal metamorphism study of the C, G, B, and F asteroids has been revisited using their UV, visible, NIR, and 3 μm reflectance spectra. High-quality reflectance spectra of seven selected C, G, B, and F asteroids have been compared with spectra for 29 carbonaceous chondrites, including thermally-metamorphosed CI/CM meteorites. There are three sets of spectral counterparts, among which 511 Davida and B-7904 are the most similar to each other in terms of both spectral shape and brightness. By comparing the 0.7 μm and 3 μm absorption strengths of 21 C, G, B, and F asteroids and heated Murchison samples, these asteroids have been grouped into three heating-temperature ranges. These correspond to (1) <400 °C: phyllosilicate-rich; (2) 400–600 °C: phyllosilicates transformed to anhydrous silicates; and (3) >600 °C: fully anhydrous. A good correlation between the UV and 3 μm absorption strengths has been confirmed for the C, G, B, and F asteroids and the CI, CM, and CR meteorites. A plot of the UV absorption strength vs. the IRAS diameter for 142 C, G, B, and F asteroids shows that the maximum UV absorption strength decreases as the diameter increases for the asteroids >60 km, with a notable exception, Ceres. These relationships suggest that some of the larger asteroids may be the heated inner portions of once larger bodies and that common CI/CM meteorites may have come from the lost outer portions, which escaped extensive late-stage heating events.     

Grain size of the surface regolith of asteroid 4 Vesta estimated from its reflectance spectrum in comparison with HED meteorites

Abstract— The grain-size distribution of the regolith of asteroid 4 Vesta has been estimated by comparing its reflectance spectra (0.3–2.6 μm) with those of HED meteorites. The finest grain-size separate (<25 μm) of a particular howardite has a reflectance spectrum most similar to Vesta's. In order to better simulate Vesta's surface mineralogy, reflectance spectra of those finest HED meteorite powders were linearly combined, and Vesta's spectrum was scaled for the best fit between them. Both the albedo and the shape of reflectance spectrum of Vesta were well reproduced by regional mixtures of the finest (<25 μm) powders of HED meteorites. The result suggests the heterogeneity of Vesta's surface and provides an estimate of the visible reflectance of Vesta that is close to its IRAS albedo. Thus, this suggests that fine grains can be generated and retained by relatively small bodies (Vesta is approximately 500 km in diameter).     

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.     

Reflectance spectroscopy of ferric sulfate-bearing montmorillonites as Mars soil analog materials

Spectroscopic analyses have shown that smectites enhanced in the laboratory with additional ferric species exhibit important similarities to those of the soils on Mars. Ferrihydrite in these chemically treated smectites has features in the visible to near-infrared region that resemble the energies and band strengths of features in reflectance spectra observed for several bright regions on Mars. New samples have been prepared with sulfate as well, because S was found by Viking to be a major component in the surface material on Mars. A suite of ferrihydrite-bearing and ferric sulfate-bearing montmorillonites, prepared with variable Fe3+ and S concentrations and variable pH conditions, has been analyzed using reflectance spectroscopy in the visible and infrared regions, M?ssbauer spectroscopy at room temperature and 4 K, differential thermal analysis, and X-ray diffraction. These analyses support the formation of ferrihydrite of variable crystallinity in the ferrihydrite-bearing montmorillonites and a combination of schwertmannite and ferrihydrite in the ferric sulfate-bearing montmorillonites. Small quantities of poorly crystalline or nanophase forms of other ferric materials may also be present in these samples. The chemical formation conditions of the ferrihydrite-bearing and ferric sulfate-bearing montmorillonites influence the character of the low temperature M?ssbauer sextets and the visible reflectance spectra. An absorption minimum is observed at 0.88-0.89 micrometers in spectra of the ferric sulfate-bearing samples, and at 0.89-0.92 micrometers in spectra of the ferrihydrate-bearing montmorillonites. M?ssbauer spectra of the ferric sulfate-bearing montmorillonites indicate variable concentrations of ferrihydrite and schwertmannite in the interlaminar spaces and along grain surfaces. Dehydration under reduced atmospheric pressure conditions induces a greater effect on the adsorbed and interlayer water in ferrihydrite-bearing montmorillonite than on the water in ferric sulfate-bearing montmorillonite. Reflectance spectra of ferric sulfate-bearing montmorillonite include a strong 3-micrometers band that is more resistant to dry atmospheric conditions than the 3-micrometers band in spectra of similarly prepared ferrihydrite-bearing montmorillonites.     

Spectral properties, magnetic fields, and dust transport at lunar swirls

Lunar swirls are albedo anomalies associated with strong crustal magnetic fields. Swirls exhibit distinctive spectral properties at both highland and mare locations that are plausibly explained by fine-grained dust sorting. The sorting may result from two processes that are fairly well established on the Moon, but have not been previously considered together. The first process is the vertical electrostatic lofting of charged fine dust. The second process is the development of electrostatic potentials at magnetic anomalies as solar wind protons penetrate more deeply into the magnetic field than electrons. The electrostatic potential can attract or repel charged fine-grained dust that has been lofted. Since the finest fraction of the lunar soil is bright and contributes significantly to the spectral properties of the lunar regolith, the horizontal accumulation or removal of fine dust can change a surface’s spectral properties. This mechanism can explain some of the spectral properties of swirls, accommodates their association with magnetic fields, and permits aspects of weathering by micrometeoroids and the solar wind.     

A visible and near-infrared photometric correction for Moon Mineralogy Mapper (M3)

Observations of the Moon obtained by the Moon Mineralogy Mapper (M³) instrument were acquired at various local viewing geometries. To compensate for this, a visible near-infrared photometric correction for the M³ observations of the lunar surface has been derived. Images are corrected to the standard geometry of 30° phase angle with an incidence of 30° and an emission of 0°. The photometric correction is optimized for highland materials but is also a good approximation for mare deposits. The results are compared with ground-based observations of the lunar surface to validate the absolute reflectance of the M³ observations. This photometric model has been used to produce the v1.0 Level 2 delivery of the entire set of M³ data to the Planetary Data System (PDS). The photometric correction uses local topography, in this case derived from an early version of the Lunar Orbiter Laser Altimeter data, to more accurately determine viewing geometry. As desired, this photometric correction removes most of the topography of the M³ measurements. In this paper, two additional improvements of the photometric modeling are discussed: (1) an extrapolated phase function long ward of 2500 nm to avoid possible misinterpretation of spectra in the wavelength region that includes possible OH/H₂O absorptions and (2) an empirical correction to remove a residual cross-track gradient in the data that likely is an uncorrected instrumental effect. New files for these two effects have been delivered to PDS and can be applied to the M³ observations.