Hyperspectral imaging of drill core from the Steen River impact structure,Canada: Implications for hydrothermal activity and formation of suevite‐like breccias

Hyperspectral imaging can be used to rapidly identify and map the spatial distributions of many minerals. Here, hyperspectral mapping in three wavelength regions (visible and near‐infrared, shortwave infrared, and thermal infrared) was applied to drill cores (ST001, ST002, and ST003) penetrating a continuous sequence of crater‐fill breccias from the Steen River impact structure in Alberta, Canada. The combined data sets reveal distinct mineralogical layering, with breccias derived predominantly from sedimentary rocks overlying those derived from granitic basement. This stratigraphy demonstrates that the breccias were not appreciably disturbed following deposition, which is inconsistent with formation models of similar breccias (suevites) by explosive impact melt–fluid interaction. At Steen River, volatiles from sedimentary target rocks were an inherent part of forming these enigmatic breccias. Approximately three quarters of terrestrial impact structures contain sedimentary target rocks; therefore, the role of volatiles in producing so‐called suevitic breccias may be more widespread than previously realized. The hyperspectral maps, specifically within the SWIR wavelength region, also delineate minerals associated with postimpact hydrothermal activity, including ammoniated clay and feldspar minerals not detectable using traditional techniques. These nitrogen‐bearing minerals may have originated from microbial processes, associated with oil‐ and gas‐producing units in the crater vicinity. Such minerals may have important implications for the production of habitable environments by impact‐induced hydrothermal activity on Earth and Mars.     

Mapping global lunar abundance of plagioclase,clinopyroxene and olivine with Interference Imaging Spectrometer hyperspectral data considering space weathering effect

Mineral mapping of the lunar surface is critical to understanding the Moon’s geological diversity and history, yet the global lunar abundance of minerals has not been mapped using hyperspectral data. The Interference Imaging Spectrometer (IIM) of Chang’E-1 mission obtained hyperspectral data of the global lunar surface within the wavelength of 480–960 nm in which major minerals can be discriminated by faint differences in 32 contiguous hyperspectral bands. The effect of space weathering produces multiple endmembers of lunar minerals by obscuring the pure spectra of minerals in different levels. In this study, the distributions of plagioclase, clinopyroxene and olivine on the global lunar surface were mapped with IIM hyperspectral data based on the modified Multiple Endmember Spectral Mixture Analysis (MESMA) method considering the space weathering effect. The distribution of lunar space weathering levels was retrieved as a byproduct of mineral mapping. The mineral mapping results were compared with recent mapping results. Although the wavelength of IIM is limited, it shows that our results are basically consistent with the recent research at both global and local scales. The distribution of space weathering levels is also consistent with the map of optical maturity parameter (OMAT) in most parts of the global lunar surface, especially in the highlands. This study demonstrates that the modified MESMA method is an effective approach to quantitative mapping of the lunar minerals and space weathering levels using hyperspectral data. In the future, more minerals can be mapped with higher accuracy if hyperspectral data with a wider spectral range are used based on the method proposed in this study.     

Stability of hydrous minerals on the martian surface

The presence of water-bearing minerals on Mars has long been discussed, but little or no data exist showing that minerals such as smectites and zeolites may be present on the surface in a hydrated state (i.e., that they could contain H₂O molecules in their interlayer or extra-framework sites, respectively). We have analyzed experimental thermodynamic and X-ray powder diffraction data for smectite and the most common terrestrial zeolite, clinoptilolite, to evaluate the state of hydration of these minerals under martian surface conditions. Thermodynamic data for clinoptilolite show that water molecules in its extra-framework sites are held very strongly, with enthalpies of dehydration for Ca-clinoptilolite up to three times greater than that for liquid water. Using these data, we calculated the Gibbs free energy of hydration of clinoptilolite and smectite as a function of temperature and pressure. The calculations demonstrate that these minerals would indeed be hydrated under the very low-P (H₂O) conditions existing on Mars, a reflection of their high affinities for H₂O. These calculations assuming the partial pressure of H₂O and the temperature range expected on Mars suggest that, if present on the surface, zeolites and Ca-smectites could also play a role in affecting the diurnal variations in martian atmospheric H₂O because their calculated water contents vary considerably over daily martian temperature ranges. The open crystal structure of clinoptilolite and existing hydration and kinetic data suggest that hydration/dehydration are not kinetically limited. Based on these calculations, it is possible that hydrated zeolites and clay minerals may explain some of the recent observations of significant amounts of hydrogen not attributable to water ice at martian mid-latitudes.     

Al‐Mg isotopic evidence for episodic alteration of Ca‐Al‐rich inclusions from Allende

Abstract— Textures, mineral assemblages, and Al‐Mg isotope systematics indicate a protracted, episodic secondary mineralization history for Allende Ca‐Al‐rich inclusions (CAIs). Detailed observations from one type B1 CAI, one B2, one compact type A (CTA), and one fluffy type A (FTA) indicate that these diverse types of CAIs are characterized by two distinct textural and mineralogic types of secondary mineralization: (1) grossular‐rich domains, concentrated along melilite grain boundaries in CAI interiors, and (2) feldspathoid‐bearing domains, confined mostly to CAI margins just interior to the Wark‐Lovering rim sequence. The Al‐Mg isotopic compositions of most secondary minerals in the type B1 CAI, and some secondary minerals in the other CAIs, show no resolvable excesses of ²⁶Mg, whereas the primary CAI phases mostly yield correlated excesses of ²⁶Mg with increasing Al/Mg corresponding to “canonical” initial ²⁶Al/²⁷Al ～ 4.5–5 × 10^?5. These secondary minerals formed at least 3 Ma after the primary CAI minerals. All but two analyses of secondary minerals from the fluffy type‐A CAI define a correlated increase in ²⁶Mg/²⁴Mg with increasing Al/Mg, yielding (²⁶Al/²⁷Al)0 = (4.9 ± 2.8) × 10^?6. The secondary minerals in this CAI formed 1.8–3.2 Ma after the primary CAI minerals. In both cases, the timing of secondary alteration is consistent with, but does not necessarily require, alteration in an asteroidal setting. One grossular from the type B2 CAI, and several grossular and secondary feldspar analyses from the compact type A CAI, have excesses of ²⁶Mg consistent with initial ²⁶Al/²⁷Al ～ 4.5 × 10^?5. Especially in the compact type A CAI, where ²⁶Mg/²⁴Mg in grossular correlates with increasing Al/Mg, these ²⁶Mg excesses are almost certainly due to in situ decay of ²⁶Al. They indicate a nebular setting for formation of the grossular. The preservation of these diverse isotopic patterns indicates that heating on the Allende parent body was not pervasive enough to reset isotopic systematics of fine‐grained secondary minerals. Secondary mineralization clearly was not restricted to a short time interval, and at least some alteration occurred coincident with CAI formation and melting events (chondrule formation) in the nebula. This observation supports the possibility that alteration followed by melting affected the compositional evolution of CAIs.     

Infrared diffuse reflectance spectra of carbonaceous chondrites: Amount of hydrous minerals

Abstract— Infrared diffuse reflectance spectra (2.53–25 μm) of some carbonaceous (C) chondrites were measured. The integrated intensity of the absorption bands near 3 μm caused by hydrous minerals were compared with the modal content of hydrous minerals for the meteorites. The CM and CI chondrites show larger values of the integrated intensity than those of the unique C chondrites Y82162, Y86720 and B7904, suggesting that the amount of hydrous minerals in the CM and CI chondrites is larger, which supports the contention that hydrous minerals were dehydrated by thermal metamorphism in the unique chondrites. Orgueil (CI) has the largest value of the integrated intensity among the C chondrites we measured and shows a sharp absorption band at 3685 cm^?1 (2.71 μm) that is not seen in the spectra of the CM chondrites. There is an excellent correlation between the observed hydrogen content in C chondrites and the integrated intensity. The CM chondrites show a wide variation in the strength of absorption bands at 1470 cm^?1 (6.8 μm), despite the similarity in absorption features near 3 μm for all CM chondrites. The 1470 cm^?1 band could be due to the presence of some hydrocarbons but may also be a result of terrestrial alteration processes.     

Shock‐induced thermal history of an EH3 chondrite,Asuka 10164

Shock‐induced features are abundantly observed in meteorites. Especially, shock veins, including high‐pressure minerals, characterize many kinds of heavily shocked meteorite. On the other hand, no high‐pressure phases have been yet reported from enstatite chondrites. We studied a heavily shocked EH3 chondrite, Asuka 10164, containing a vein, which comprises fragments of fine‐grained silicate and opaque minerals, and chondrules. In this vein, we found a silica polymorph, coesite. This is the first discovery of a high‐pressure phase in enstatite chondrites. Other high‐pressure polymorphs were not observed in the vein. The assemblages and chemical compositions of minerals, and the occurrence of coesite indicate that the vein was subjected to the high‐pressure and temperature condition at about 3–10 GPa and 1000 °C. The host also experienced heating for a short time under lower temperature conditions, from ~700 to ~1000 °C, based on the opaque minerals typical of EH chondrites and textural features. Although the pressure condition of the vein in this chondrite is much lower than those in the other meteorites, our results suggest that all major meteorite groups contain high‐pressure polymorphs. Heavy shock events commonly took place in the solar system.     

The Northwest Africa (NWA) 5790 meteorite: A mesostasis‐rich nakhlite with little or no Martian aqueous alteration

Northwest Africa (NWA) 5790 is the most recently discovered member of the nakhlite group. Its mineralogy differs from the other nakhlites with a high abundance mesostasis (38.1 ± 3.6 vol%) and scarcity of olivine (4.0 ± 2.2 vol%). Furthermore, zoning of augite phenocrysts, and other petrographic and chemical characteristics suggest that NWA 5790 samples the chilled margin of its parent lava flow/sill. NWA 5790 contains calcite and rare clay minerals that are evidence for its exposure to liquid water. The calcite forms a cement to coatings of dust on the outer surface of the find and extends into the interior of the meteorite within veins. The presence of microbial remains within the coating confirms that the dust and its carbonate cement are terrestrial in origin, consistent with the carbon and oxygen isotope composition of the calcite. The clay minerals are finely crystalline and comprise ~0.003 vol% of the meteorite. δD values of the clay minerals range from ?212 ± 109‰ to ?96 ± 132‰, and cannot be used to distinguish between a terrestrial or Martian origin. As petrographic results are also not definitive, we conclude that secondary minerals produced by Martian groundwaters are at best very rare within NWA 5790. The meteorite has therefore sampled a region of the lava flow/sill with little or no exposure to the aqueous solutions that altered other nakhlites. This isolation could relate to the scarcity of olivine in NWA 5790 because dissolution of olivine in other nakhlites by Martian groundwaters enhanced their porosity and permeability, and provided solutes for secondary minerals.     

The ubiquitous presence of silica-rich glass inclusions in mafic minerals: Examples from Earth,Mars, Moon and the aubrite parent body

Abstract— Highly silicic glass inclusions are commonly present in mafic minerals of xenolithic terrestrial upper mantle rocks (Schiano and Clocchiatti, 1994). They are believed to be the products of volatile-rich silicic melts for which several sources have been proposed (Francis, 1976; Frey and Green, 1974; Schiano et al, 1995), but their origin(s) and, consequently, that of the glasses, remains unknown. However, in situ formation by very low-degree partial melting seems to be possible as has been shown by experiments (e.g., Baker et al, 1995; Draper and Green, 1997). Glass inclusions of silicic chemical composition are also present in some mafic minerals of achondritic meteorites (e.g., Fuchs, 1974; Okada et al, 1988; Johnson et al, 1991). The enstatite achondrites (aubrites) Aubres and Norton County, which record early planetesimal and planet formation in the solar nebula, and the olivine achondrite (chassignite) Chassigny, a rock believed to originate from Mars, contain abundant glass inclusions in their main minerals enstatite and olivine, respectively. Glasses of glass-bearing inclusions have a highly silicic and volatile-rich chemical composition similar, but not identical, to that of glass inclusions in terrestrial upper mantle peridotite minerals. Furthermore, glass inclusions in olivines from the Moon (e.g., Roedder and Weiblen, 1977) are also silica-rich. Because different physicochemical conditions prevail in the source regions of these rocks, the process of melting is, perhaps, not generally applicable for the generation of silica-rich glasses. Alternatively, the glasses could have been formed via precipitation from silicate-loaded fluids (Schneider and Eggler, 1986) or vapors. Another possible mechanism, not previously identified, could be dehydrogenation of nominally nonhydrous mafic minerals by heating or depressurization that should be accompanied by expulsion of excess silica and incompatible elements. This process will mimic low-temperature, very low-degree partial melting. It could account also for the highly variable glass/bubble ratios observed in glass inclusions in aubrite enstatites. We suggest that such a process could have been operating in the solar nebula, the Moon and Mars, and could be operating still on Earth.     

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.     

Silica minerals in cumulate eucrites: Insights into their thermal histories

Some eucrites contain up to 10 vol% silica minerals; however, silica minerals have not been studied in detail so far. We performed a mineralogical study of silica minerals in three cumulate eucrites (Moore County, Moama, and Yamato [Y] 980433). Monoclinic tridymite was common in all three samples. Moama contained orthorhombic tridymite as lamellae within monoclinic tridymite grains. Y 980433 included quartz around an impact melt vein. The presence of orthorhombic tridymite in Moama indicates that Moama cooled more rapidly than the other two samples at low temperatures (<400 °C). This result is different from the slower cooling rates of Moama (?0.0004 °C yr^?1) than that of Moore County (>0.3 °C yr^?1, after the shock event) at high temperatures (>500 °C) estimated from compositional profiles of pyroxene exsolution lamellae. The difference of the cooling rates may reflect their geological settings. Y 980433 cooled slowly at low temperature, as did Moore County. Quartz in Y 980433 could be a local product transformed from monoclinic tridymite by a shock event. We suggest that silica minerals in meteorites record thermal histories at low temperatures and shock events.     

Analysis of phyllosilicate deposits in the Nili Fossae region of Mars: Comparison of TES and OMEGA data

Diverse phyllosilicate deposits discovered previously in the Nili Fossae region with near infrared reflectance data are a window into the complex history of aqueous alteration on Mars. In this work, we used thermal infrared data from the Thermal Emission Spectrometer (TES) in combination with near infrared data from the Observatoire pour la Minéralogie, l’Eau, les Glaces, et l’Activité (OMEGA) to better constrain the mineralogy and geologic origin of these deposits. We developed a TES spectral index for identification of clay minerals, which correctly identifies the phyllosilicates in the Nili Fossae area and points to several other interesting deposits in the Syrtis Major region. However, detailed inspection of the TES spectral features of Nili Fossae phyllosilicates shows a feature at low wavenumbers (350-550 cm⁻¹) that is not an exact match to any specific Fe³⁺-, Al-, or Mg-rich phyllosilicate phase. Instead, the feature is more similar to basaltic glass and may indicate that the phyllosilicates in this region are: (1) rich in Fe²⁺ (based on similarity to trends seen in laboratory data of clay minerals), (2) poorly crystalline/extremely disordered, and/or (3) present within a matrix of actual basalt glass. This feature is similar to spectral features seen in altered rocks in the Columbia Hills region of Gusev Crater by previous authors. By calibrating measured spectral index values against mathematical spectral mixtures of typical martian dark surfaces and known abundances of alteration minerals, we are able to estimate an enrichment in abundance of alteration minerals in the altered surfaces. Many dark, Noachian deposits in the Nili Fossae area are enriched phyllosilicates by 20-30% (±10-15%) relative to dark, volcanic surfaces in the same region. The distribution and abundance of these phases indicates that alteration in the region was pervasive, but did not completely erase the original mineralogy of what was likely an Fe-rich basalt protolith. As a group, the Nili Fossae phyllosilicate deposits are fundamentally different from those found in the Mawrth Vallis region. Nili Fossae deposits have strong thermal infrared features related to admixed pyroxene, plagioclase, and occasionally olivine, whereas the Mawrth Vallis deposits contain no mafic minerals. Comparison of TES and OMEGA data also illustrates some more general differences between the datasets, including the impact of physical character of the martian surface on detectability of minerals in each spectral range.     

The Cretaceous-Tertiary fireball layer,ejecta layer and coal seam: Platinum-group element content and mineralogy of size fractions

Abstract— Grain size separates of the Cretaceous-Tertiary (K-T) fireball layer at marine sites and the entire K-T boundary interval at nonmarine sites (fireball layer, ejecta layer, coal seam) were analysed for platinum-group elements (PGE: Ru, Ir, Ft, Pd, Rh) and Au using inductively coupled plasma mass-spectrometry. X-ray diffractometry and scanning electron microscopy were performed on each fraction to establish the mineralogy. It was determined that the most abundant minerals in the finest fraction were a smectite-group mineral at marine K-T sites and illite-smectite mixed layer clay at nonmarine K-T sites. Positive correlation of PGE content and mineralogy indicates that the PGE are presently associated with these clay minerals which were likely formed by alteration of a condensed mafic phase (e.g., olivine or pyroxene). The correlation of clay mineral abundance with PGE content is imperfect because not all of the clay minerals in the fireball layer are derived by alteration of the original condensed ejecta. In addition, undetected PGE host(s), present in trace amounts, are likely also present.     

High‐pressure minerals in shocked meteorites

Heavily shocked meteorites contain various types of high‐pressure polymorphs of major minerals (olivine, pyroxene, feldspar, and quartz) and accessory minerals (chromite and Ca phosphate). These high‐pressure minerals are micron to submicron sized and occur within and in the vicinity of shock‐induced melt veins and melt pockets in chondrites and lunar, howardite–eucrite–diogenite (HED), and Martian meteorites. Their occurrence suggests two types of formation mechanisms (1) solid‐state high‐pressure transformation of the host‐rock minerals into monomineralic polycrystalline aggregates, and (2) crystallization of chondritic or monomineralic melts under high pressure. Based on experimentally determined phase relations, their formation pressures are limited to the pressure range up to ~25 GPa. Textural, crystallographic, and chemical characteristics of high‐pressure minerals provide clues about the impact events of meteorite parent bodies, including their size and mutual collision velocities and about the mineralogy of deep planetary interiors. The aim of this article is to review and summarize the findings on natural high‐pressure minerals in shocked meteorites that have been reported over the past 50 years.     

Experimental hydrothermal alteration of a martian analog basalt: Implications for martian meteorites

Abstract— A number of martian meteorite samples contain secondary alteration minerals such as Ca‐Mg‐Fe carbonates, Fe oxides, and clay minerals. These mineral assemblages hint at hydrothermal processes occurring in the martian crust, but the alteration conditions are poorly constrained. This study presents the results of experiments that examined the alteration of a high‐Fe basalt by CO₂‐saturated aqueous fluids at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C and water‐rock ratios of 1:1 and 1:10. Results indicate that observable alteration of the basalt takes place after runs of only seven days. This alteration includes mobilization of silica into phases such as opal‐CT and quartz, as well as the formation of carbonates, oxides, and at some conditions, zeolites and hydrous silicates. The degree of alteration increases with run temperature and, in high‐temperature vapor experiments, with increasing water content of the vapor. The degree of alteration and the mineralogy observed in the martian meteorites suggests that none of these samples were exposed to aqueous fluids for long periods of time. Nakhla and Lafayette probably interacted with water for relatively brief periods of time; if so, silica may have been leached from the parent rocks by the altering fluids. Allan Hills 84001 shows possible evidence for very limited interaction with an aqueous fluid, but the overall slight degree of alteration described for this meteorite strongly suggests that it never interacted extensively or at high temperature with any water‐bearing fluid. Elephant Moraine A79001 may not have been altered by aqueous fluids at all. The results of this study best support models wherein the meteorite parent rocks were wetted intermittently or for brief periods of time rather than models that invoke long‐term reaction with large volumes of water. Our experiments studied alteration of a high‐Fe basalt by dilute, CO₂‐saturated, aqueous solutions at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C. The results suggest that alteration of the parent rock takes place even after very short reaction times of seven days. All experiments produced carbonate minerals, including calcite, and in some cases, magnesite, siderite, and ankerite. A free silica phase, either opal, quartz, or hydrated silica, formed in most experiments. More altered experiments also contained minerals such as zeolites and hydrous phyllosilicates. Clay minerals were not observed to form in any experiments. In aqueous fluids, higher temperature corresponded with a higher degree of alteration, whereas changing fluid composition had no observable effect. In high‐temperature vapors, the degree of alteration was controlled by temperature and the proportion of H₂O to CO₂, with water‐rock ratio also playing a role in transport of silica. Application of these results to martian meteorites that contain secondary alteration minerals suggests that none of the martian rocks underwent extensive interaction with aqueous fluids. Nakhla and Lafayette contain clay minerals, which suggests that they interacted with water to some extent, possibly at elevated temperatures. Although ALH84001 shows possible evidence of very limited interaction with aqueous fluids, EETA79001 does not. These results support models for the alteration of these meteorites that do not invoke long‐term interaction with water or reaction with large volumes of water. Except for some models for alteration of ALH84001, this conclusion agrees with most of the literature on alteration of martian meteorites.     

An analysis of open-basin lake deposits on Mars: Evidence for the nature of associated lacustrine deposits and post-lacustrine modification processes

A large number of candidate open-basin lakes (low-lying regions with both inlet valleys and an outlet valley) have been identified and mapped on Mars and are fed by valley network systems that were active near the Noachian–Hesperian boundary. The nature of processes that modified the open-basin lake interiors subsequent to lacustrine activity, and how frequently sedimentary deposits related to lacustrine activity remain exposed, has not been extensively examined. An analysis of 226 open-basin lakes was undertaken to identify evidence for: (1) exposed deposits of possible lacustrine origin and (2) post-lacustrine-activity processes that may have modified or resurfaced open-basin lakes. Spectroscopic data from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) instrument were analyzed over identified exposed open-basin lake deposits to assess the mineralogy of these deposits. Particular attention was paid to the possible detection of any component of aqueous alteration minerals (e.g. phyllosilicates, hydrated silica, zeolites) or evaporites (e.g. carbonates, sulfates, chlorides) associated with these exposed deposits. The aim of this paper is to act as a broad survey and cataloguing of the types of lacustrine and post-lacustrine deposits that are present within these 226 paleolake basins. Results of the morphologic classification indicate that 79 open-basin lakes (～35% of the population) contain exposed deposits of possible lacustrine origin, identified on the basis of fan/delta deposits, layered deposits and/or exposed floor material of apparent lacustrine origin. Additionally, all 226 open-basin lakes examined appear to have been at least partially resurfaced subsequent to their formation by several processes, including volcanism, glacial and periglacial activity, impact cratering and aeolian activity. Results from the analysis of CRISM data show that only 10 (～29% of the 34 deposits with CRISM coverage) of the exposed open-basin lake deposits contain positively identified aqueous alteration minerals, with one deposit also containing evaporites. The identified hydrated and evaporite minerals include Fe/Mg-smectite, kaolinite, hydrated silica and carbonate, with Fe/Mg-smectite the most commonly identified mineral. These results indicate that hydrated and evaporite minerals are not as commonly associated with lacustrine deposits on Mars as they are on Earth. This suggests in situ alteration and mineral precipitation, a common source of such minerals in terrestrial lakes, was not a major process occurring in these paleo-lacustrine systems, and that the observed minerals are likely to be present as transported material within the lacustrine deposits. The lack of widespread in situ alteration also suggests that either the water chemistry in these paleolake systems was not conducive to aqueous alteration and mineral precipitation, or that the open-basin lake systems were relatively short-lived.     

Mineralogy and petrogenesis of lunar magnesian granulitic meteorite Northwest Africa 5744

Lunar meteorite Northwest Africa (NWA) 5744 is a granulitic breccia with an anorthositic troctolite composition that may represent a distinct crustal lithology not previously described. This meteorite is the namesake and first‐discovered stone of its pairing group. Bulk rock major element abundances show the greatest affinity to Mg‐suite rocks, yet trace element abundances are more consistent with those of ferroan anorthosites. The relatively low abundances of incompatible trace elements (including K, P, Th, U, and rare earth elements) in NWA 5744 could indicate derivation from a highlands crustal lithology or mixture of lithologies that are distinct from the Procellarum KREEP terrane on the lunar nearside. Impact‐related thermal and shock metamorphism of NWA 5744 was intense enough to recrystallize mafic minerals in the matrix, but not intense enough to chemically equilibrate the constituent minerals. Thus, we infer that NWA 5744 was likely metamorphosed near the lunar surface, either as a lithic component within an impact melt sheet or from impact‐induced shock.     

Petrology and origin of amoeboid olivine aggregates in CR chondrites

Abstract— Amoeboid olivine aggregates (AOAs) are irregularly shaped, fine‐grained aggregates of olivine and Ca, Al‐rich minerals and are important primitive components of CR chondrites. The AOAs in CR chondrites contain FeNi metal, and some AOAs contain Mn‐rich forsterite with up to 0.7 MnO and Mn:Fe ratios greater than one. Additionally, AOAs in the CR chondrites do not contain secondary phases (nepheline and fayalitic olivine) that are found in AOAs in some CV chondrites. The AOAs in CR chondrites record a complex petrogenetic history that included nebular gas‐solid condensation, reaction of minerals with the nebular gas, small degrees of melting, and sintering of the assemblage. A condensation origin for the Mn‐rich forsterite is proposed. The Mn‐rich forsterite found in IDPs, unequilibrated ordinary chondrite matrix, and AOAs in CR chondrites may have had a similar origin. A type A calcium, aluminum‐rich inclusion (CAI) with an AOA attached to its Wark‐Lovering rim is also described. This discovery reveals a temporal relationship between AOAs and type A inclusions. Additionally, a thin layer of forsterite is present as part of the Wark‐Lovering rim, revealing the crystallization of olivine at the end stages of Wark‐Lovering rim formation. The Ca, Al‐rich nodules in the AOAs may be petrogenetically related to the Ca, Al‐rich minerals in Wark‐Lovering rims on type A CAIs. AOAs are chondrite components that condensed during the final stage of Wark‐Lovering rim formation but, in general, were temporally, spatially, or kinetically isolated from reacting with the nebula vapor during condensation of the lower temperature minerals that were commonly present as chondrule precursors.     

Spectral Models of Kuiper Belt Objects and Centaurs

We present models of the spectral reflectances of groups of outer Solar System objects defined primarily by their colors in the spectral region 0.4–1.2 mu;m, and which have geometric albedo ～0.04 at wavelength 0.55 μm. Our models of the groups with the strongest reflectance gradients (reddest colors) use combinations of organic tholins. We test the hypothesis that metal-reddened igneous rock-forming minerals contribute to the red colors of Centaurs and KBOs by using the space-weathered lunar soil as one of the components of our models. We find that our models can admit the presence of moderate amounts of space-weathered (metal-reddened) minerals, but that they do not require this material to achieve the red colors of the reddest outer Solar System bodies. Our models with organic tholins are consistent with the results of other investigators.     

The chemical variation of moldavite tektites: Simple mixing of terrestrial sediments

Abstract— To test different hypotheses of moldavite formation, a major and trace-element study of 25 moldavite tektites and Sm-Nd isotope measurement of three moldavite tektites was completed. The samples were selected from the classical substrewnfields and the newly described locations in Lusatia (Saxony, Germany). Samples with unusual bulk composition were also included. The results confirm earlier studies that the variation in the chemical composition can be explained by single impact and through incomplete mixing of at least three lithographical components dominated by one of the three minerals or mineral groups: dolomite, clay minerals and quartz. An additional endmember, possibly a rare Earth's mantle component, containing high Co, Cr and Ni concentrations is also needed to explain the observed variations in compatible elements of some tektites. Volatile element abundances are low but not necessarily the result of selective volatilization.     

COLLESCIPOLI: AN UNUSUAL FUSION CRUST GLASS

An electron microprobe study was conducted on glass fragments taken from the fusion crust and an internal glass-lined vein in the H-5 chondrite Collescipoli. Microprobe analyses of the glasses revealed an unusual fusion crust composition, and analyses of glass from inside the meteorite showed compositions expected for a melt of an H-group chondrite. Studies of fusion crusts by previous workers, e.g., Krinov and Ramdohr, showed that fusion crusts contain large amounts of magnetite and other oxidized minerals. The Collescipoli fusion crusts do contain these minerals, but they also contain relatively large amounts of reduced metal, sulphide, and a sodium-rich glass. This study seems to indicate that Collescipoli preserved an early type of fusion crust. Oxidation was incomplete in the fusion crust melt that drained into a crack. From this study it is concluded that fusion crust formation does not invariably result in complete oxidation of metal and sulphide phases.