Pyroxene microstructure in the Northwest Africa 856 martian meteorite

Abstract— Transmission electron microscopy was used to examine pyroxene microstructure in the Northwest Africa (NWA) 856 martian meteorite to construct its cooling and shock histories. All pyroxenes contain strained coherent pigeonite/augite exsolution lamellae on (001). The average width and periodicity of lamellae are 80 and 400 nm, respectively, indicating a cooling rate below 0.1 °C/hr for the parent rock. Pigeonite and augite are topotactic, with strained coherent interfaces parallel to (001). The closure temperature for Ca‐Fe, Mg interdiffusion, estimated from the composition at the augite pigeonite interface, is about 700 °C. Tweed texture in augite reveals that a spinodal decomposition occurred. Locally, tweed evolved toward secondary pigeonite exsolutions on (001). Due to the decreasing diffusion rate with decreasing temperature, “M‐shaped” concentration profiles developed in augite lamellae. Pigeonite contains antiphase boundaries resulting from the C2/c to P2₁/c space group transition that occurred during cooling. The reconstructive phase transition from P2₁/c clinopyroxene to orthopyroxene did not occur. The deformation (shock) history of the meteorites is revealed by the presence of dislocations and mechanical twins. Dislocations are found in glide configuration, with the [001](100) glide system preferentially activated. They exhibit strong interaction with the strained augite/pigeonite interfaces and did not propagate over large distances. Twins are found to be almost all parallel to (100) and show moderate interaction with the augite/pigeonite interfaces. These twins are responsible for the plastic deformation of the pyroxene grains. Comparison with microstructure of shocked clinopyroxene (experimentally or naturally shocked) suggests that NWA 856 pyroxenes are not strongly shocked.     

Trace ferric ion in lunar and meteoritic titanaugites

Evidence for presence of Fe³⁺ in lunar rocks is furnished by heating them in air to 200-225°C for two hours. This causes a large decrease in the same charge transfer bands attributed to Fe³⁺ that can be enhanced by heating the same rocks in air at 500°C. This data is interpreted as evidence that the Fe³⁺ was not in equilibrium in the melt but was produced by cosmic radiation subsequent to the rock formation. The decrease of the Fe³⁺ charge-transfer bands is accompanied by decrease in intensity of spin-allowed Fe²⁺ bands attributed toM ₁ sites in the pyroxene in rock 12018. This decrease in the Fe²⁺ bands is attributed to decrease in the Fe²⁺ Fe³⁺ charge-transfer intensification of these Fe²⁺ spin-allowed transitions when radiation-produced Fe³⁺ is partially-reduced by the low-temperature heating.The reaction of Fe³⁺ on heating to 200-225°C is probably Fe³⁺ + Ti³⁺ Fe²⁺ + Ti⁴⁺.This is the reverse of the reaction caused by cosmic ray bombardment of the rock on the lunar surface. Possible tetrahedrally coordinated Fe³⁺ is present in the meteoritic and lunar augites as suggested by comparison of their spectra to that of terrestrial augite high in Fe³⁺. This would have been present in the original melt and is distinct from radiation produced Fe³⁺ in theM-sites.The polarized absorption spectra of single crystal pigeonite and augite from rock 12021 before heating, and augite from 12018 after heating are compared to that of meteoritic titanaugite in the Angra dos Reis meteorite and terrestrial titanaugite from Maui, Hawaii. The absorption spectrum of meteoritic hypersthene (Tatahouine) is also included for comparison to the pigeonite.     

Polarized absorption spectra of single crystals of lunar pyroxenes and olivines

Measurements have been made of the polarized absorption spectra (360-2200 nm.) of compositionally zoned pyroxene minerals in rocks 10045, 10047 and 10058 and olivines in rocks 10020 and 10022. Specimens in the form of petrographic thin sections were mounted on polarizing microscopes equipped with three-axis universal stage attachments and inserted into a Cary 17 spectrophotometer. The Apollo 11 pyroxenes with relatively high Ti/Fe ratios were chosen initially to investigate the presence of crystal field spectra of Fe²⁺ and Ti³⁺ ions in the minerals.Broad intense bands at about 1000 and 2100 nm. arise from spin-allowed, polarization-dependent transitions in Fe²⁺ ions in pyroxenes. Several weak sharp peaks occur in the visible region. Peaks at 402, 425, 505, 550 and 585 nm. represent spin-forbidden transitions in Fe²⁺ ions, while broader bands at 460–470 nm. and 650–660 nm. are attributed to Ti³⁺ ions. Charge transfer bands, which in terrestrial pyroxenes often extend into the visible region, are displaced to shorter wavelengths in lunar pyroxenes. This feature correlates with the absence of Fe³⁺ ions in these minerals. The magnitudes of the intensity ratios: band 465 nm. (Ti³⁺) to band 1000 nm. (Fe²⁺) are similar to Ti/Fe ratios from lunar pyroxene bulk chemical analyses, suggesting that an appreciable amount of titanium occurs as Ti³⁺ ions in the lunar pyroxenes. The 505 nm. spin-forbidden peak in Fe²⁺, together with absorption at 465 nm. by Ti³⁺, contribute to the pink or pale reddish-brown colors of lunar pyroxenes in transmitted lights.The absorption spectral measurements not only provide information on the redox behavior and crystal chemistry of lunar pyroxenes, but also form a basis for interpreting spectral reflectivity properties of lunar rocks and the Moon's surface.     

Anisotropy of absorption bands in some lunar,meteoritic, and terrestrial pyroxenes

The optical anisotropy of individual spin-forbidden transitions of Fe³⁺ and Fe²⁺ ions and spin-allowed transitions of Ti³⁺ and of Fe²⁺ ions are observed in complex clinopyroxene crystals in lunar rock in both the pigeonite core and the augite overgrowth. Spectral bands are compared to similar ones in terrestrial augite from Maui, Hawaii, meteoritic augite in the Angra dos Reis achondrite, meteoritic shocked hypersthene in the Tatahauine achondrite and meteoritic diopside in the Nakhla achondrite.The maxima of Fe³⁺ ion-ligand charge-transfer bands in the ultraviolet are compared in these minerals.Paper dedicated to Professor Harold C. Urey on the occasion of his 80th birthday on 29 April, 1973.     

Mineralogy of Antarctic basaltic shergottite Queen Alexandra Range 94201: Similarities to Elephant Moraine A79001 (Lithology B) martian meteorite

Abstract— Antarctic meteorite QUE 94201 is a new basaltic shergottite that is mainly composed of subequal amounts of maskelynite and pyroxenes (pigeonite and augite) plus abundant merrillite and accessory phases. It also contains impact melt. Complex zoning patterns in QUE 94201 pyroxenes revealed by elemental map analyses using an electron microprobe suggest a crystallization sequence from Mg-rich pigeonite (En₆₂Fss₃₀Wo_g) to extremely Fe-rich pigeonite (En₅Fs₈₁Wo₁₄) via {110} Mg-rich augite bands (En₄₄Fs₂₀Wo₃₆) in a single crystal. These textures, along with the abundant plagioclase (maskelynite), indicates single-stage rapid cooling (>5 °C/year) of this rock from a supercooled magma. Transition from Mg-rich augite to Fe-rich pigeonite reflects the onset of plagioclase crystallization. Enrichment of late-stage phases in QUE 94201 implies crystallization from an evolved magma and suggests a different parent magma composition from the other basaltic shergottites. Lithology B of EETA79001 basaltic shergottite contains pyroxenes that show complex zoning with augite bands similar to those in QUE 94201 pyroxene, which suggests similar one-stage rapid cooling. Lithology B of EETA79001 also resembles QUE 94201 in its coarse-grained texture of silicates and its high abundance of maskelynite, although QUE 94201 probably crystallized from a more fractionated magma. We also note that some Apollo lunar mare basalts (e.g., 12020 and 12021) have similar mineralogy and petrology to QUE 94201, especially in pyroxene zoning. All these basaltic rocks with complex pyroxene zoning suggest rapid metastable crystallization from supercooled magmas.     

Mineralogy and cooling history of the calcium-aluminum-chromium enriched ureilite,Lewis Cliff 88774

Abstract— The LEW 88774 ureilite is extraordinarily rich in Ca, Al, and Cr, and mineralogically quite different from other ureilites in that it consists mainly of exsolved pyroxene, olivine, Cr-rich spinel, and C. The presence of coarse exsolved pyroxene in LEW 88774 is unique because pyroxene in most other ureilites is not exsolved. The pyroxene has bulk Wo contents of 15–20 mol% and has coarse exsolution lamellae of augite and low-Ca pyroxene, 50 μm in width. The compositions of the exsolved augite (Ca_33.7Mg_52.8Fe_13.5) and host low-Ca pyroxene (Ca_4.4Mg₇₅Fe_20.6) show that these exsolution lamellae were equilibrated at 1280 °C. A computer simulation of the cooling rate, obtained by solving the diffusion equation for reproducing the diffusion profile of CaO across the lamellae, suggests that the pyroxene was cooled at 0.01 °C/year until the temperature reached 1160 °C. This cooling rate corresponds to a depth of at least 1 km in the parent body, assuming it was covered by a rock-like material. Therefore, LEW 88774 was held at this high temperature for 1.2 × 10⁴years. The proposed cooling history is consistent with that of other ureilites with coarsegrained unexsolved pigeonites. Lewis Cliff 88774 includes abundant Cr-rich spinel in comparison with other ureilites. The range of FeO content of spinels in LEW 88774 is from 1.3 wt% to 21 wt% [Fe/(Fe + Mg) = 0.04–0.6]. The Cr-rich and Fe-poor spinel in LEW 88774 has less Fe (FeO, 1.3 wt%) than spinels in other achondrites. We classify this spinel as an Fe, Al-bearing picrochromite. Most ureilites are depleted in Ca and Al, but this meteorite has high-Ca and Al concentrations. In this respect, as well as mineral assemblage and the presence of coarse exsolution lamellae in pyroxene, LEW 88774 is a unique ureilite. Most differentiated meteorites are poor in volatile elements such as Zn, but the LEW 88774 spinels contain abundant Zn (up to 0.6 wt%). We note that such a high Zn concentration in spinel has been observed in the carbonaceous chondrites and recrystallized chondrites. This unusual ureilite has more primitive characteristics than most other ureilites.     

Valence state partitioning of V between pyroxene‐melt: Effects of pyroxene and melt composition,and direct determination of V valence states by XANES. Application to Martian basalt QUE 94201 composition

Abstract— Experiments on a Martian basalt composition show that D_v augite/melt is greater than D_v pigeonite/melt in samples equilibrated under the same fO₂ conditions. This increase is due to the increased availability of elements for coupled substitution with the V³⁺ or V⁴⁺ ions, namely A1 and Na. For this bulk composition, both A1 and Na are higher in concentration in augite compared with pigeonite; therefore more V can enter augite than pigeonite. Direct valence state determination by XANES shows that the V³⁺ and V⁴⁺ are the main V species in the melt at fO₂ conditions of IW‐1 to IW+3.5, whereas pyroxene grains at IW‐1, IW, and IW+1 contain mostly V³⁺. This confirms the idea that V³⁺ is more compatible in pyroxene than V⁴⁺. The XANES data also indicates that a small percentage of V²⁺ may exist in melt and pyroxene at IW‐1. The similar valence of V in glass and pyroxene at IW‐1 suggests that V²⁺ and V³⁺ may have similar compatibilities in pyroxene.     

Microtextures and crystal chemistry of pigeonite in the ureilites ALHA77257, RKPA80239, Y‐791538, and ALHA81101

Abstract— The microtextures of pigeonite in four ureilites, Allan Hills (ALH) 77257, Reckling Peak (RKP) A80239, Yamato (Y‐) 791538, and Allan Hills A81101, chosen to span a range of composition and shock level, were investigated by transmission electron microscopy (TEM); two of the samples were also investigated by single crystal X‐ray diffraction to determine Fe²⁺‐Mg cation site partitioning. The low‐shock and compositionally homogeneous pigeonites in ALHA77257 and RKPA80329 (Wo 6.4 for both, mg 86.3 and 84.3 respectively) display irregularly spaced, shock‐induced stacking faults oriented parallel to (100), and large antiphase domains (50–100 nm). Antiphase domains have no preferential orientation. No evidence of exsolution was observed. The low‐shock Y‐791538 pigeonite is homogeneous and has higher Ca and mg (Wo 9.4, mg 91.2). TEM investigation showed spinodal decomposition, indicative of incipient exsolution; small antiphase domains were observed (～5 nm). Single crystal refinement yielded R_4s? = 5.71%, with Fe²⁺‐Mg partitioning coefficient k_d = 0.077(8) and T_c = 658(35) °C. ALHA81101 has compositionally heterogeneous pyroxenes, with large local variations in Wo and mg (Wo = 4–13, mg = 86–68). No compositional gradients from core to rim of grains were observed, and the heterogeneity is interpreted as related to cation migration during shock. In one relatively Ca‐rich region (Wo～12), TEM analysis showed augite‐pigeonite exsolution lamellae, with spacing 145(20) nm. Results for ALHA77257, RKPA80239, and Y‐791538 support a model of rapid cooling following breakup of the ureilite parent body. The presence of exsolution lamellae in ALHA81101 can be related to a local shock‐induced Ca enrichment and provides no constraint on the late cooling history.     

Thermal history of the Ibitira noncumulate eucrite as inferred from pyroxene exsolution lamella: Evidence for reheating and rapid cooling

Abstract— Ibitira is a strongly recrystallized and unbrecciated noncumulate eucrite. We measured Ca compositional profiles of Ibitira pyroxene by electron microprobe and computed the cooling rate and burial depth from pyroxene exsolution profiles to gain information on early thermal history of Ibitira. Pyroxene begins to exsolve at 1082 °C and cools down to 550 °C at a rate of 0.02 °C/year, forming an augite lamella about 7.0 μm in width. A notable characteristic of the Ca profile of augite lamellae in Ibitira pyroxene is a gradient near the interface between augite and low‐Ca pyroxene (pigeonite). This profile suggests that after thermal metamorphism Ibitira pyroxene experienced a sudden temperature rise to above solidus temperature of pyroxene (～1082 °C), and subsequent rapid cooling. The ³⁹Ar‐⁴⁰Ar age of 4.485 Ga for Ibitira, which is the oldest ³⁹Ar‐⁴⁰Ar age for noncumulate eucrites, may date this reheating event.     

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.     

Regolith breccia Northwest Africa 7533: Mineralogy and petrology with implications for early Mars

Northwest Africa 7533, a polymict Martian breccia, consists of fine‐grained clast‐laden melt particles and microcrystalline matrix. While both melt and matrix contain medium‐grained noritic‐monzonitic material and crystal clasts, the matrix also contains lithic clasts with zoned pigeonite and augite plus two feldspars, microbasaltic clasts, vitrophyric and microcrystalline spherules, and shards. The clast‐laden melt rocks contain clump‐like aggregates of orthopyroxene surrounded by aureoles of plagioclase. Some shards of vesicular melt rocks resemble the pyroxene‐plagioclase clump‐aureole structures. Submicron size matrix grains show some triple junctions, but most are irregular with high intergranular porosity. The noritic‐monzonitic rocks contain exsolved pyroxenes and perthitic intergrowths, and cooled more slowly than rocks with zoned‐pyroxene or fine grain size. Noritic material contains orthopyroxene or inverted pigeonite, augite, calcic to intermediate plagioclase, and chromite to Cr‐bearing magnetite; monzonitic clasts contain augite, sodic plagioclase, K feldspar, Ti‐bearing magnetite, ilmenite, chlorapatite, and zircon. These feldspathic rocks show similarities to some rocks at Gale Crater like Black Trout, Mara, and Jake M. The most magnesian orthopyroxene clasts are close to ALH 84001 orthopyroxene in composition. All these materials are enriched in siderophile elements, indicating impact melting and incorporation of a projectile component, except for Ni‐poor pyroxene clasts which are from pristine rocks. Clast‐laden melt rocks, spherules, shards, and siderophile element contents indicate formation of NWA 7533 as a regolith breccia. The zircons, mainly derived from monzonitic (melt) rocks, crystallized at 4.43 ± 0.03 Ga (Humayun et al. 2013 ) and a ¹⁴⁷Sm‐¹⁴³Nd isochron for NWA 7034 yielding 4.42 ± 0.07 Ga (Nyquist et al. 2016 ) defines the crystallization age of all its igneous portions. The zircon from the monzonitic rocks has a higher Δ¹⁷O than other Martian meteorites explained in part by assimilation of regolith materials enriched during surface alteration (Nemchin et al. 2014 ). This record of protolith interaction with atmosphere‐hydrosphere during regolith formation before melting demonstrates a thin atmosphere, a wet early surface environment on Mars, and an evolved crust likely to have contaminated younger extrusive rocks. The latest events recorded when the breccia was on Mars are resetting of apatite, much feldspar and some zircons at 1.35–1.4 Ga (Bellucci et al. 2015 ), and formation of Ni‐bearing pyrite veins during or shortly after this disturbance (Lorand et al. 2015 ).     

A TEM study of exsolution in Ca-rich pyroxenes from the Paris and Renazzo chondrites: Determination of type I chondrule cooling rates

We conducted a transmission electron microscope study of the exsolution microstructures of Ca-rich pyroxenes in type I chondrules from the Paris CM and Renazzo CR carbonaceous chondrites in order to provide better constraints on the cooling history of type I chondrules. Our study shows a high variability of composition in the augite grains at a submicrometer scale, reflecting nonequilibrium crystallization. The microstructure is closely related to the local composition and is thus variable inside augite grains. For compositions inside the pyroxene miscibility gap, with a wollastonite (Wo) content typically below 40 mole%, the augite grains contain abundant exsolution lamellae on (001). For grain areas with composition close to Wo₄₀, a modulated texture on (100) and (001) is the dominant microstructure, while areas with compositions higher than Wo₄₀ do not show any exsolution microstructure development. To estimate the cooling rate, we used the spacing of the exsolution lamellae on (001), for which the growth is diffusion controlled and thus sensitive to the cooling rate. Despite the relatively homogeneous microstructures of augite grains with Wo < 35 mole%, our study of four chondrules suggests a range of cooling rates from ~10 to ~1000 °C h⁻¹, within the temperature interval 1200–1350 °C. These cooling rates are comparable to those of type II chondrules, i.e., 1–1000 °C h⁻¹. We conclude that the formation of type I and II chondrules in the proto-solar nebula was the result of a common mechanism.     

The 506 nm absorption feature in pyroxene spectra: Nature and implications for spectroscopy-based studies of pyroxene-bearing targets

High-resolution (0.34 nm) reflectance spectra of a suite of terrestrial ortho- and clinopyroxenes were characterized in the 506-nm region. This region exhibits absorption bands attributed to spin-forbidden transitions in Fe²⁺ located in the M2, and possibly M1, crystallographic site(s). The most intense absorption bands (up to 3.8% deep in <45 μm fractions) are present in low Ca-content orthopyroxene spectra. This region exhibits two (spectral Group I) or more (spectral Group II) absorption bands in the 500-515 nm interval. Group I spectra are associated with the lowest Ca-content samples. For orthopyroxenes, the number of constituent absorption bands and band depths vary as a function of Ca content; increasing Ca content results the appearance of more than two absorption bands and a general reduction in band depths, offsetting an expected increase in band depth with increasing Fe²⁺ content; band depths may also be reduced due to the long wavelength wing of ultraviolet region Fe-O charge transfer absorptions. Band depths and shapes in this region are also a function of grain size, with the strongest bands appearing for larger grain sizes - in the 90-250 μm range. The number and position of constituent absorption bands can be used to constrain factors such as cooling rates, as expressed in the formation of Guinier-Preston zones versus coarser-grained augite exsolution lamellae. Band depths in the spectra of fine-grained (<45 μm) clinopyroxenes do not exceed 1% and are generally lowest for spectral type A clinopyroxenes, where most of the Fe²⁺ is present in the M1 crystallographic site. The appearance of the 506 nm band in the spectra of pyroxene-bearing asteroids can be used to constrain pyroxene composition and structure. The results of this study suggest that detailed analysis of absorption features in the 506 nm region is a powerful tool for determining the composition and structure of pyroxenes. The spectral resolution of the VIR-MS spectrometer aboard the Dawn spacecraft - which will examine Asteroid 4 Vesta, a body possessing surficial pyroxenes - will be sufficient to provide some constraints on pyroxene composition.     

Northwest Africa 773: Lunar origin and iron‐enrichment trend

Abstract— The meteorite Northwest Africa 773 (NWA 773) is a lunar sample with implications for the evolution of mafic magmas on the moon. A combination of key parameters including whole‐rock oxygen isotopic composition, Fe/Mn ratios in mafic silicates, noble gas concentrations, a KREEP‐like rare earth element pattern, and the presence of regolith agglutinate fragments indicate a lunar origin for NWA 773. Partial maskelynitization of feldspar and occasional twinning of pyroxene are attributed to shock deformation. Terrestrial weathering has caused fracturing and precipitation of Carich carbonates and sulfates in the fractures, but lunar minerals appear fresh and unoxidized. The meteorite is composed of two distinct lithologies: a two‐pyroxene olivine gabbro with cumulate texture, and a polymict, fragmental regolith breccia. The olivine gabbro is dominated by cumulate olivine with pigeonite, augite, and interstitial plagioclase feldspar. The breccia consists of several types of clasts but is dominated by clasts from the gabbro and more FeO‐rich derivatives. Variations in clast mineral assemblage and pyroxene Mg/(Mg + Fe) and Ti/(Ti + Cr) record an igneous Fe‐enrichment trend that culminated in crystallization of fayalite + silica + hedenbergite‐bearing symplectites. The Fe‐enrichment trend and cumulate textures observed in NWA 773 are similar to features of terrestrial ponded lava flows and shallow‐level mafic intrusives, indicating that NWA 773 may be from a layered mafic intrusion or a thick, differentiated lava flow. NWA 773 and several other mafic lunar meteorites have LREE‐enriched patters distinct from Apollo and Luna mare basalts, which tend to be LREE‐depleted. This is somewhat surprising in light of remote sensing data that indicates that the Apollo and Luna missions sampled a portion of the moon that was enriched in incompatible heatproducing elements.     

The oxidation state of nanophase Fe particles in lunar soil: Implications for space weathering

We report measurements of the oxidation state of Fe nanoparticles within lunar soils that experienced varied degrees of space weathering. We measured >100 particles from immature, submature, and mature lunar samples using electron energy‐loss spectroscopy (EELS) coupled to an aberration‐corrected transmission electron microscope. The EELS measurements show that the nanoparticles are composed of a mixture of Fe⁰, Fe²⁺, and Fe³⁺ oxidation states, and exhibit a trend of increasing oxidation state with higher maturity. We hypothesize that the oxidation is driven by the diffusion of O atoms to the surface of the Fe nanoparticles from the oxygen‐rich matrix that surrounds them. The oxidation state of Fe in the nanoparticles has an effect on modeled reflectance properties of lunar soil. These results are relevant to remote sensing data for the Moon and to the remote determination of relative soil maturities for various regions of the lunar surface.     

Accretionary mixing of a eucrite impactor and the regolith of the L chondrite parent body

Northwest Africa (NWA) 869 is the largest sample of chondritic regolith breccia, making it an ideal source for research on accretionary processes and primordial chemical mixing. One such process can be seen in detail through the first identification of a eucrite impactor clast in an L chondrite breccia. The ~7 mm diameter clast has oxygen isotope compositions (Δ¹⁷O = ?0.240, ?0.258‰) and pigeonite and augite compositions typical for eucrites, but with high areal abundance of silica (9.5%) and ilmenite (1.5%). The rim around the clast is a mixture of breccia and igneous phases, the latter due to either impactor‐triggered melting or later metamorphism. The rim has an oxygen isotope composition falling on a mixing line between known eucrite and L chondrite compositions (Δ¹⁷O = 0.326‰) and, coincidentally, on the Mars fractionation line. Pyroxene grains from the melt component in the rim have compositions that fall on a mixing line between the average eucrite pyroxene composition and equilibrated L chondrite composition. The margins of chondritic olivine crystal clasts in the rim are enriched in Fe as a result of diffusion from the Fe‐rich melt and suggest cooling on the scale of hours. The textures and chemical mixing observed provide evidence for an unconsolidated L chondrite target material, differing from the current state of NWA 869 material. The heterogeneity of oxygen isotope and chemical signatures at this small length scale serve as a cautionary note when extrapolating from small volumes of materials to deduce planetesimal source characteristics.     

Thermal and shock history of Almahata Sitta meteorite inferred from structure refinement of pyroxene and Mössbauer spectroscopy of Fe-Ni metal

The crystal structures of orthopyroxene (En_86.3Fs_8.6Wo_5.1, space group Pbca) and pigeonite (En_81.7Fs_8.8Wo_9.5, space group P2₁/c) from the Almahata Sitta ureilite (fragment#051) have been refined to R1 indices of 3.10% and 2.53%, respectively, using single-crystal X-ray diffraction data. The unit formulas were calculated from electron microprobe analysis, and the occupancies at the M1 and M2 sites were refined for both pyroxenes from the single-crystal diffraction data. The results indicate a rather disordered intracrystalline Fe²⁺-Mg cation distribution over the M1 and M2 sites, with a closure temperature of 726(±55)°C for orthopyroxene and 704(±110)°C for pigeonite, suggesting fast cooling of these pyroxenes. The Mössbauer spectrum of the Fe-Ni metal particles of Almahata Sitta ureilite (fragment#051) is dominated by two overlapping magnetic sextets that are assigned to Fe atoms in Si-bearing kamacite, and arise from two different nearest-neighbor configurations of Fe* (=Fe+Ni) and Si atoms in the bcc structure of kamacite; (8F*, 0Si) and (7Fe*, 1Si). In addition, the spectrum shows weak absorption peaks that are attributed to the presence of small amounts of cohenite [(Fe,Ni)₃C], schreibersite [(Fe,Ni)₃P], and an Fe-oxide/hydroxide phase. The fast cooling of pyroxene to the closure temperature (after equilibration at ~1200°C) and the incorporation of Si in kamacite can be interpreted as due to a shock event that took place on the meteorite parent body, consistent with the proposed formation history of ureilites parent body where a fast cooling has occurred at a later stage of its formation.     

STUDIES OF BRAZILIAN METEORITES XIV. MINERALOGY,PETROLOGY, AND CHEMISTRY OF THE CONQUISTA,MINAS GERAIS,CHONDRITE

The Conquista chondrite consists of major olivine, low-Ca pyroxene (both ortho- and twinned clino-), troilite and metallic nickel-iron; minor glassy to microcrystalline material and pigeonite; and accessory chromite, high-Ca clinopyroxene and hydrous ferric oxides that formed by terrestrial weathering of metallic nickel-iron. Results of microscopic, electron microprobe, and bulk chemical studies, particularly the compositions of olivine (Fa_17.2) and low-Ca pyroxene (Fs_15.4); the contents of metallic nickel-iron (18.5%) and total iron (25.83%); and the ratios of Fe°/Fe_total (0.64), Fe°/Ni° (9.59) and Fe_total/SiO₂ (0.69) indicate H-group classification. The pronounced, well-developed chondritic texture; the slight compositional variations in constituent phases; the high Ca contents of pyroxene and the presence of pigeonite, glassy to microcrystalline interstitial material rich in alkalis and SiO₂, and of twinned low-Ca clinopyroxene suggest that Conquista is of petrologic type 4.     

Evidence of space weathering in regolith breccias II: Asteroidal regolith breccias

Abstract– Space weathering products, such as agglutinates and nanophase iron‐bearing rims are easily preserved through lithification in lunar regolith breccias, thus such products, if produced, should be preserved in asteroidal regolith breccias as well. A study of representative regolith breccia meteorites, Fayetteville (H4) and Kapoeta (howardite), was undertaken to search for physical evidence of space weathering on asteroids. Amorphous or npFe⁰‐bearing rims cannot be positively identified in Fayetteville, although possible glass rims were found. Extensive friction melt was discovered in the meteorite that is difficult to differentiate from weathered materials. Several melt products, including spherules and agglutinates, as well as one irradiated rim and one possible npFe⁰‐bearing rim were identified in Kapoeta. The existence of these products suggests that lunar‐like space weathering processes are, or have been, active on asteroids.     

Reflectance spectra of analog anorthosites: Implications for lunar highland mapping

Lunar highland region and associated craters are mostly composed of anorthosite. In the present study, we studied the reflectance spectra of terrestrial anorthosites collected from Sittampundi Anorthosites Complex, which is considered as equivalent (simulant) of lunar highland anorthosites. The objective of the study is to interpret diagnostic spectral features of analog anorthosite for remotely exploring lunar highland region. Reflectance spectra of anorthosites were measured under two different environments, such as controlled field and laboratory conditions. In these two procedures, the laboratory spectra give clear, diagnostic spectral information in the present study. Reflectance spectra captured under 350-2500 nm covering UV, Visible, NIR, and SWIR part of the electromagnetic spectrum. The spectral characteristics of anorthosites measured under various parts of electromagnetic spectrum have diagnostic absorption features at 380-387, 700-740, 930-1100, 1160-1200, 1415, 1920, 2200 and 2330 nm correspondingly due to plagioclase UV absorption, Fe³⁺ electron transition absorption, Fe²⁺ pyroxene and olivine absorption, OH/Mn³⁺ crystal transition absorption, pyroxene absorption, Al-OH absorption and Mg-OH absorption. Mineralogical and chemical analyses were carried out for four anorthosites and compared with the results of chemical component of lunar anorthosite. The percentage of plagioclase content, relative abundance of low and high calcium pyroxene and olivine in different anorthosite samples are correlated with the albedo range, absorption shape, absorption centers and band depth. The similarity in the diagnostic spectral features of the anolog anorthosite with lunar anorthosites could be effectively utilized for remotely mapping the lunar highland region.