Influence of plasma on formation of crystalline Fe2SiO4 grains

The production of Fe₂SiO₄ (fayalite) crystalline grains was performed by two processes, namely, grain formation in a plasma field by evaporating a mixture powder of Fe and SiO and heat treatment of the product collected on the radio-frequency (RF) electrode side. Fe grains <20 nm in size covered with an amorphous SiO layer selectively formed Fe₂SiO₄ grains by heating at 800 °C. By heating at 600 °C, in addition to the formation of Fe₂SiO₄ crystal grains, the FeO phase appeared. The doping effect of excited oxygen in a plasma field into the Fe small grains may be the trigger on the formation of fayalite through the FeO phase formation. The present experimental result suggests that the probability of Fe₂SiO₄ grain formation in space is low.     

Demonstration of crystalline forsterite grain formation due to coalescence growth of Mg and SiO smoke particles

Abstract— Experimental studies of coalescence between Mg grains and SiO grains in smoke reveal the direct production of crystalline forsterite grains. The present results also show that different materials can be produced by grain‐grain collisions, which have been considered one of the models of grain formation in the interstellar medium. The fundamentals of coalescence growth in smoke, which have been developed in our series of experiments, are presented in this paper. Mg₂Si polyhedral grains were obtained in a Mg grain‐rich atmosphere. Mg₂SiO₄ polyhedral grains were obtained in a SiO grain‐rich atmosphere. The IR spectra of the resultant grains showed the characteristics of crystalline forsterite.     

FT-IR microspectroscopy of extraterrestrial dust grains: Comparison of measurement techniques

Identification of astronomical dust composition rests on comparison of Infrared (IR) spectra with standard laboratory spectra; frequently, however, a single mineralogical composition is assumed for spectral matching. Advances in laboratory instrumentation have enabled very precise IR spectra to be measured on single grains and zones within grains; with a more complete set of spectral data for planetary dust, better compositional matches will be achieved for astronomical dust. We have compared several FT-IR spectroscopy techniques (open path transmission spectroscopy and diffuse reflectance spectroscopy of powders; microspectroscopy of single grains and powders and ATR spectroscopy of thin sections) to determine their utility for the direct measurement of the mid-IR spectra of small amounts of extraterrestrial grains. We have focussed our investigation on the spectra of the olivine series of silicates, (Mg,Fe)₂SiO₄, a species frequently identified as one of the major constituents of interstellar dust. The positions of three characteristic SiO₄ stretching bands at ∼10.4, 11.3 and 12 μm were measured for comparison of the techniques. All methods gave satisfactory results, although care must be taken to guard against artefacts from sample thickness and orientation effects. Single grains hand-picked from meteorites can be analysed, but results are inaccurate if the grain size is too large (>1-10 μm). Spectra for single grains also show variations that arise from sample orientation effects. Once the analytical artefacts are taken into account, we found that measurement of powder with a diamond compression cell is best suited for the analysis of small amounts of materials.     

Ferrous silicate spherules with euhedral iron‐nickel metal grains from CH carbonaceous chondrites: Evidence for supercooling and condensation under oxidizing conditions

Abstract— The CH carbonaceous chondrites contain a population of ferrous (Fe/(Fe + Mg) ? 0.1‐0.4) silicate spherules (chondrules), about 15–30 μm in apparent diameter, composed of cryptocrystalline olivinepyroxene normative material, ±SiO₂‐rich glass, and rounded‐to‐euhedral Fe, Ni metal grains. The silicate portions of the spherules are highly depleted in refractory lithophile elements (CaO, Al₂O₃, and TiO₂ <0.04 wt%) and enriched in FeO, MnO, Cr₂O₃, and Na₂O relative to the dominant, volatile‐poor, magnesian chondrules from CH chondrites. The Fe/(Fe + Mg) ratio in the silicate portions of the spherules is positively correlated with Fe concentration in metal grains, which suggests that this correlation is not due to oxidation, reduction, or both of iron (FeO_sil ? Fe_met) during melting of metal‐silicate solid precursors. Rather, we suggest that this is a condensation signature of the precursors formed under oxidizing conditions. Each metal grain is compositionally uniform, but there are significant intergrain compositional variations: about 8–18 wt% Ni, <0.09 wt% Cr, and a sub‐solar Co/Ni ratio. The precursor materials of these spherules were thus characterized by extreme elemental fractionations, which have not been observed in chondritic materials before. Particularly striking is the fractionation of Ni and Co in the rounded‐to‐euhedral metal grains, which has resulted in a Co/Ni ratio significantly below solar. The liquidus temperatures of the euhedral Fe, Ni metal grains are lower than those of the coexisting ferrous silicates, and we infer that the former crystallized in supercooled silicate melts. The metal grains are compositionally metastable; they are not decomposed into taenite and kamacite, which suggests fast postcrystallization cooling at temperatures below 970 K and lack of subsequent prolonged thermal metamorphism at temperatures above 400–500 K.     

Space weathering of silicates simulated by successive laser irradiation: In situ reflectance measurements of Fo90, Fo99+, and SiO2

Pulsed‐laser irradiation causes the visible‐near‐infrared spectral slope of olivine (Fo₉₀ and Fo₉₉₊) and SiO₂ to increase (redden), while the olivine samples darken and the SiO₂ samples brighten slightly. XPS analysis shows that irradiation of Fo₉₀ produces metallic Fe. Analytical SEM and TEM measurements confirm that reddening in the Fo₉₀ olivine samples correlates with the production of “nanophase” metallic Fe (npFe⁰) grains, 20–50 nm in size. The reddening observed in the SiO₂ sample is consistent with the formation of SiO or other SiO_x species that absorb in the visible. The weak spectral brightening induced by laser irradiation of SiO₂ is consistent with a change in surface topography of the sample. The darkening observed in the olivine samples is likely caused by the formation of larger npFe⁰ particles, such as the 100–400 nm diameter npFe⁰ identified during our TEM analysis of Fo₉₀ samples. The Fo₉₀ reflectance spectra are qualitatively similar to those in previous experiments suggesting that in all cases formation of npFe⁰ is causing the spectral alteration. Finally, we find that the accumulation of successive laser pulses cause continued sample darkening in the Vis‐NIR, which suggests that repeated surface impacts are an efficient way to darken airless body surfaces.     

Iron oxides in comet 81P/Wild 2

Abstract– We have used synchrotron Fe‐XANES, XRS, microRaman, and SEM‐TEM analyses of Stardust track 41 slice and track 121 terminal area slices to identify Fe oxide (magnetite‐hematite and amorphous oxide), Fe‐Ti oxide, and V‐rich chromite (Fe‐Cr‐V‐Ti‐Mn oxide) grains ranging in size from 200 nm to ～10 μm. They co‐exist with relict FeNi metal. Both Fe‐XANES and microRaman analyses suggest that the FeNi metal and magnetite (Fe₂O₃FeO) also contain some hematite (Fe₂O₃). The FeNi has been partially oxidized (probably during capture), but on the basis of our experimental work with a light‐gas gun and microRaman analyses, we believe that some of the magnetite‐hematite mixtures may have originated on Wild 2. The terminal samples from track 121 also contain traces of sulfide and Mg‐rich silicate minerals. Our results show an unequilibrated mixture of reduced and oxidized Fe‐bearing minerals in the Wild 2 samples in an analogous way to mineral assemblages seen in carbonaceous chondrites and interplanetary dust particles. The samples contain some evidence for terrestrial contamination, for example, occasional Zn‐bearing grains and amorphous Fe oxide in track 121 for which evidence of a cometary origin is lacking.     

MINERALOGY,PETROLOGY AND CHEMISTRY OF LUNAR ROCK 12039

Rock 12039 belongs to the olivine-depleted group of magmatic rocks characterized by normative and modal SiO₂, absence or very low abundance of olivine, and high FeO/(FeO + MgO), Ti/Cr, and CaO/MgO ratios. Clinopyroxenes in this rock show a complex, essentially continuous, compositional zonation from augite cores through ferroaugite to ferrohedenbergite with an abrupt discontinuity at the pyroxferroite contact and, thus, are different from pyroxene in most other Apollo 12 rocks. Two grains contain thin subcalcic pigeonite zones. Texture, presence of very fine (< 1 μm) exsolution lamallae, and pyroxene zoning indicate a relatively rapid cooling history and pronounced in situ chemical fractionation. Rock 12039, on the basis of mineralogy and bulk composition, is the most highly differentiated member of the olivine-depleted basalt group     

Laboratory analogy of crystalline enstatite grain formation in plasma field

Crystalline enstatite (MgSiO₃) grains were produced by the simultaneous evaporation of SiO grains and Mg vapor in a plasma field. The MgSiO₃ grains were spherical or needlelike. The necessity of a plasma field in astromineralogy is suggested in the present study.     

Ambient and cold‐temperature infrared spectra and XRD patterns of ammoniated phyllosilicates and carbonaceous chondrite meteorites relevant to Ceres and other solar system bodies

Mg‐phyllosilicate‐bearing, dark surface materials on the dwarf planet Ceres have NH₄‐bearing materials, indicated by a distinctive 3.06 μm absorption feature. To constrain the identity of the Ceres NH₄‐carrier phase(s), we ammoniated ground particulates of candidate materials to compare their spectral properties to infrared data acquired by Dawn's Visible and Infrared (VIR) imaging spectrometer. We treated Mg‐, Fe‐, and Al‐smectite clay minerals; Mg‐serpentines; Mg‐chlorite; and a suite of carbonaceous meteorites with NH₄‐acetate to exchange ammonium. Serpentines and chlorites showed no evidence for ammoniation, as expected due to their lack of exchangeable interlayer sites. Most smectites showed evidence for ammoniation by incorporation of NH₄⁺ into their interlayers, resulting in the appearance of absorptions from 3.02 to 3.08 μm. Meteorite samples tested had weak absorptions between 3.0 and 3.1 μm but showed little clear evidence for enhancement upon ammoniation, likely due to the high proportion of serpentine and other minerals relative to expandable smectite phases or to NH₄⁺ complexing with organics or other constituents. The wavelength position of the smectite NH₄ absorption showed no variation between IR spectra acquired under dry‐air purge at 25 °C and under vacuum at 25 °C to ?180 °C. Collectively, data from the smectite samples show that the precise center wavelength of the characteristic ~3.05 μm v₃ absorption in NH₄ is variable and is likely related to the degree of hydrogen bonding of NH₄‐H₂O complexes. Comparison with Dawn VIR spectra indicates that the hypothesis of Mg‐saponite as the ammonium carrier phase is the simplest explanation for observed data, and that Ceres dark materials may be like Cold Bokkeveld or Tagish Lake but with proportionally more Mg‐smectite.     

Raman spectroscopic properties and Raman identification of CaS‐MgS‐MnS‐FeS‐Cr2FeS4 sulfides in meteorites and reduced sulfur‐rich systems

Raman spectra were acquired on a series of natural and synthetic sulfide minerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite ((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr₂FeS₄). Natural samples come from three enstatite chondrites, three aubrites, and one anomalous ungrouped enstatite meteorite. Synthetic samples range from pure endmembers (CaS, FeS, MgS) to complex solid solutions (Fe, Mg, Ca)S. The main Raman peaks are localized at 225, 285, 360, and 470 cm^?1 for the Mg‐rich sulfides; at 185, 205, and 285 cm^?1 for the Ca‐rich sulfides; at 250, 370, and 580 cm^?1 for the Mn‐rich sulfides; at 255, 290, and 365 cm^?1 for the Cr‐rich sulfides; and at 290 and 335 cm^?1 for troilite with, occasionally, an extra peak at 240 cm^?1. A peak at 160 cm^?1 is present in all Raman spectra and cannot be used to discriminate between the different sulfide compositions. According to group theory, none of the cubic monosulfides oldhamite, niningerite, or alabandite should present first‐order Raman spectra because of their ideal rocksalt structure. The occurrence of broad Raman peaks is tentatively explained by local breaking of symmetry rules. Measurements compare well with the infrared frequencies calculated from first‐principles calculations. Raman spectra arise from activation of certain vibrational modes due to clustering in the solid solutions or to coupling with electronic transitions in semiconductor sulfides.     

A thermodynamic model of high temperature lava vaporization on Io

We modified the MAGMA chemical equilibrium code developed by Fegley and Cameron (1987, Earth Planet. Sci. Lett. 82, 207-222) and used it to model vaporization of high temperature silicate lavas on Io. The MAGMA code computes chemical equilibria in a melt, between melt and its equilibrium vapor, and in the gas phase. The good agreement of MAGMA code results with experimental data and with other computer codes is demonstrated. The temperature-dependent pressure and composition of vapor in equilibrium with lava is calculated from 1700 to 2400 K for 109 different silicate lavas in the ONaKFeSiMgCaAlTi system. Results for five lavas (tholeiitic basalt, alkali basalt, Barberton komatiite, dunite, and a molten type B1 Ca, Al-rich inclusion) are discussed in detail. The effects of continuous fractional vaporization on chemistry of these lavas and their equilibrium vapor are presented. The predicted abundances (relative to Na) of K, Fe, Si, Al, Ca, and Ti in the vapor equilibrated with lavas at 1900 K are lower than published upper limits for Io's atmosphere (which do not include Mg). We predict evaporative loss of alkalis, Fe, and Si during volcanic eruptions. Sodium is more volatile than K, and the Na/K ratio in the gas is decreased by fractional vaporization. This process can match Io's atmospheric Na/K ratio of 10±3 reported by Brown (2001, Icarus 151, 190-195). Silicon monoxide is an abundant species in the vapor above lavas. Spectroscopic searches are recommended for SiO at IR and mm wavelengths. Reactions of metallic vapors with S- and Cl-bearing volcanic gases may form other unusual gases including MgCl₂, MgS, MgCl, FeCl₂, FeS, FeCl, and SiS.     

A DETAILED CHEMICAL STUDY ON THE BARWISE CHONDRITE

Six fragments of the Barwise meteorite were analyzed for REE and eleven other elements (Al, Ca, Mg, Mn, Na, K, Cr, Fe, Co, Ni and Ba). In addition, two fragments were analyzed for Si and Mg. The chondrite-normalized REE patterns of six fragments studied show interesting systematic variations. Three fragments with relatively high La abundances show a negative Ce anomaly. Since the meteorite in question is a find, it could be suspected that the observed REE fractionations are due to terrestrial contamination. To examine this point, a soil sample from the find site was also analyzed for REE and major chemical elements. It is considered that several facts, especially, the relationships between La and SiO₂ and between SiO₂ and MgO, suggest the pre-terrestrial fractionation rather than the terrestrial contamination. Unexpectedly, it is shown that the REE fractionation observed in the investigated fragments correlates with the metal-silicate and the Fe-Co-Ni fractionations. In this connection, large metal grains were investigated for Fe, Co and Ni contents. A suggestion is presented that this chondrite was formed through the melting of the surface of a planetesimal and the subsequent collision, although the possibility of terrestrial contamination might not be ruled out.     

The formation of Mg,Fe‐silicates by reactions between amorphous magnesiosilica smoke particles and metallic iron nanograins with implications for comet silicate origins

This thermal annealing experiment at 1000 K for up to 167 h used a physical mixture of vapor phase‐condensed magnesiosilica grains and metallic iron nanograins to test the hypothesis that a mixture of magnesiosilica grains and an Fe‐source would lead to the formation of ferromagnesiosilica grains. This exploratory study found that coagulation and thermal annealing of amorphous magnesiosilica and metallic grains yielded ferromagnesiosilica grains with the Fe/(Fe + Mg) ratios in interplanetary dust particles. Furthermore, decomposition of brucite present in the condensed magnesiosilica grains was the source for water and the cause of different iron oxidation states, and the formation of amorphous Fe³⁺‐ferrosilica, amorphous Fe³⁺‐Mg, Fe‐silicates, and magnesioferrite during thermal annealing. Fayalite and ferrosilite that formed from silica/FeO melts reacted with forsterite and enstatite to form Mg, Fe‐silicates. The presence of iron in different oxidation states in extraterrestrial materials almost certainly requires active asteroid‐like parent bodies. If so, the possible presence of trivalent Fe compounds in comet P/Halley suggests that Halley‐type comets are a mixture of preserved presolar and processed solar nebula dust. The results from this thermal annealing experiment further suggest that the Fe‐silicates detected in the impact‐induced ejecta from comet 9P/Temple 1 might be of secondary origin and related to the impact experiment or to processing in a regolith.     

The smallest comet 81P/Wild 2 dust dances around the CI composition

The bulbous Stardust track #80 (C2092,3,80,0,0) is a huge cavity. Allocations C2092,2,80,46,1 nearest the entry hole and C2092,2,80,47,6 about 0.8 mm beneath the entry hole provide evidence of highly chaotic conditions during capture. They are dominated by nonvesicular low‐Mg silica glass instead of highly vesicular glass found deeper into this track which is consistent with the escape of magnesiosilica vapors generated from the smallest comet grains. The survival of delicate (Mg,Al,Ca)‐bearing silica glass structures is unique to the entry hole. Both allocations show a dearth of surviving comet dust except for a small enstatite, a low‐Ca hypersthene grain, and a Ti‐oxide fragment. Finding scattered TiO₂ fragments in the silica glass could support, but not prove, TiO₂ grain fragmentation during hypervelocity capture. The here reported dearth in mineral species is in marked contrast to the wealth of surviving silicate and oxide minerals deeper into the bulb. Both allocations show Fe‐Ni‐S nanograins dispersed throughout the low‐Mg silica glass matrix. It is noted that neither comet Halley nor Wild 2 had a CI bulk composition for the smallest grains. Using the analogs of interplanetary dust particles (IDPs) and cluster IDPs it is argued that a CI chondritic composition requires the mixing of nonchondritic components in the appropriate proportions. So far, the fine‐grained Wild 2 dust is biased toward nonchondritic ferromagnesiosilica materials and lacking contributions of nonchondritic components with Mg‐Fe‐Ni‐S[Si‐O] compositions. To be specific, “Where are the GEMS”? The GEMS look‐alike found in this study suggests that evidence of GEMS in comet Wild 2 may still be found in the Stardust glass.     

Silica‐rich igneous rims around magnesian chondrules in CR carbonaceous chondrites: Evidence for condensation origin from fractionated nebular gas

Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO₂ phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr₂O₃) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na₂O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO_(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.     

THE ORO GRANDE,NEW MEXICO,CHONDRITE AND ITS LITHIC INCLUSION

The Oro Grande, New Mexico, U.S.A., chondrite was found in 1971. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 19.3 mole percent), orthopyroxene (Fs 16.2 mole percent), diopside, feldspar (An 13.6 mole percent), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. A bulk chemical analysis of the meteorite shows the following results (weight percent): Fe 0.84, Ni 1.46, Co 0.07, FeS 3.62, SiO₂ 34.18, TiO₂ 0.14, Al₂O₃ 1.83, Cr₂O₃ 0.55, Fe₂O₃ 21.25, FeO 9.13, MnO 0.31, MgO 21.52, CaO 1.72, Na₂O 0.70, K₂O 0.08, P₂O₅ 0.25, H₂O+ 2.14, H₂O^- 0.40, C 0.22, Sum 100.41. On the basis of composition and texture, the Oro Grande meteorite is classified as an H5 chondrite. A large lithic fragment (～5 mm long) with a very fine-grained texture different from that of the host meteorite was analyzed for bulk composition using the broad beam of an electron microprobe, and was found to be enriched in Ca, Al, Na, and K, and depleted in Mg and Fe relative to the bulk composition of the host meteorite. Its mineral compositions, however, are very similar to those of the host. It is suggested that the fragment is not a xenolith of a previously undescribed type of achondrite, but is probably an impact-produced partial melt of the host chondrite or a fragment of an unusually large chondrule.     

Can silicon monoxide grains be responsible for the interstellar 9.7 micrometer absorption band?

In this paper results of an experimental investigation of the spectra of submicrometersized silicon monoxide grains are presented. The grains manufactured from commercial SiO were prepared according to the Jena IR spectroscopy program for particulates of cosmic importance. The comparison of the laboratory spectra with those derived by means of Mie calculations using published refractive indices of bulk SiO revealed a fundamental discrepancy concerning the number and the positions of the bands. Therefore, the experimental SiO grains are suggested to change their internal structural state by the heating connected with the pressing of the KBr pellets, where the grains are embedded in. This sensitivity against heating by some hundred K rules out that SiO grains can be responsible for the 9.7 m circumstellar as well as interstellar spectral feature.     

Anatomy of individual agglutinates from a lunar highland soil

Abstract— We report results of our investigation of the relationship between values of I_s/FeO (relative concentration of nanophase Fe⁰ divided by total FeO content), glass abundance, total Fe content, and degree of digestion of <20 μm clasts for 22 individual agglutinates (250–1000 μm) from the mature Apollo 16 soil 61181 (I_s/FeO = 82 units in the <250 μm fraction). Agglutinates are important products of space weathering on the Moon, and they influence spectral observations at visible and near-IR wavelengths. Values of I_s/FeO for individual agglutinates (250–1000 μm) within this single soil span a range from 3 to 262 units which is larger than the range observed for all Apollo 16 bulk soils (～0 to 110 units). No correlation was observed between I_s/FeO and glass abundance and FeO concentrations for either agglutinitic glass or whole agglutinate particles under investigation. Our results suggest that the variation in I_s/FeO for agglutinates from a single soil may be in part a consequence of natural mixing processes on the Moon that produce highly-variable environments (with respect to surface exposure) for agglutinate formation and in part to variable kinetics of reactions in an agglutinate melt, which are influenced by a variety of factors including melt composition, temperature, impactor velocity, and quench rate. We cannot exclude but do not see evidence for other processes including addition of exotic agglutinates, micrometeoritic bombardment into compositionally-diverse microtargets, recycling of agglutinates, preferential melting of very fine soil particles, and production of nanophase Fe⁰ in amorphous rims of very fine irradiated lunar grains contributing to the observed variation of I_s/FeO.     

A condensation model for the formation of chondrules in enstatite chondrites

Abstract— It is proposed that the chondrules in enstatite chondrites formed near the Sun from rain‐like supercooled liquid silicate droplets and condensed Fe‐Ni alloys in thermodynamic equilibrium with a slowly cooling nebula. FeO formed and dissolved in the droplets in an initial stage when the nucleation of iron was blocked, and was later mostly reduced to unalloyed Fe. At high temperatures, the silicate droplets contained high concentrations of the less volatile components CaO and Al₂O₃. At somewhat lower temperatures the equilibrium MgO content of the droplets was relatively high. As cooling progressed, some droplets gravitated toward the Sun, and moved in other directions, depleting the region in CaO, Al₂O₃, and MgO and accounting for the relatively low observed CaO/SiO₂, Al₂O₃/SiO₂, and MgO/SiO₂ ratios in enstatite chondrites. At approximately 1400 K, the remaining supercooled silicate droplets crystallized to form MgSiO₃ (enstatite) with small amounts of olivine and a high‐SiO₂ liquid phase which became the mesostases. The high enstatite content is the result of the supercooled chondrules crystallizing at a relatively low temperature and relatively high total pressure. Finally, FeS formed at temperatures below 680 K by reaction of the condensed Fe with H₂S. All calculations were performed with the evaluated optimized thermodynamic databases of the FactSage thermodynamic computer system. The thermodynamic properties of compounds and solutions in these databases were optimized completely independently of any meteoritic data. Agreement of the model with observed bulk and phase compositions of enstatite chondrules is very good and is generally within experimental error limits for all components and phases.     

Petrology and geochemistry of feldspathic impact‐melt breccia Abar al' Uj 012, the first lunar meteorite from Saudi Arabia

Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al₂O₃, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An_96.9Ab_3.0Or_0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm² exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO₂ than any mare basalt. It also has higher FeO and lower Al₂O₃ than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.