Petrogenesis of Allan Hills 84001: Constraints from impact‐melted feldspathic and silica glasses

Abstract— Compositional and textural relationships of shock‐melted glasses in the Allan Hills (ALH) 84001 meteorite have been examined by optical microscopy, electron microprobe analysis, and compositional mapping. The feldspathic and silica glasses exhibit features which constrain the relative timing of shock events and carbonate deposition in ALH 84001. The feldspathic glasses are stoichiometric and have compositions plausibly described as forming from igneous plagioclase (An_27–39Ab_58–68Or_3–7) or sanidine (Or₅₁Ab₄₆An₃), or from a mixture of these phases (mixed‐feldspar glasses). These observations argue against prior interpretations of feldspathic glasses as unflowed maskelynite, hydrothermal precipitates or alteration products, or shock melts that have undergone alkali volatilization. Carbonate was deposited around previously formed mixed‐feldspar glass clasts, suggesting that carbonate deposition occurred after the shock event that formed the granular bands (crushed zones) in this meteorite. SiO₂‐rich glasses appear to be silica remobilized during shock, with little addition of other material. A petrogenetic history of ALH 84001 consistent with the observations of feldspathic and silica glasses is (1) igneous crystallization and cumulate formation; (2) a pre‐carbonate shock event that formed the granular bands (crushed zones) and sheared chromites, and melted igneous plagioclase and sanidine to form mixed‐feldspar glasses; (3) carbonate and silica deposition in the granular bands (veining of plagioclase glasses by SiO₂ and deposition of carbonate around mixed‐feldspar and plagioclase glass clasts); (4) a post‐carbonate shock event that resulted in invasion of carbonate by feldspathic melts, shock faulting and decarbonation of carbonate, high‐temperature mobilization of silica melts, and minor dissolution of orthopyroxene by silica melts.     

Transmission electron microscopy of minerals in the martian meteorite Allan Hills 84001

Abstract— We have studied carbonate and associated oxides and glasses in a demountable section of Allan Hills 84001 (ALH 84001) using optical, scanning, and transmission electron microscopy (TEM) to elucidate their origins and the shock history of the rock. Massive, fracture‐zone, and fracture‐filling carbonates in typical locations were characterized by TEM, X‐ray microanalysis, and electron diffraction in a comprehensive study that preserved textural and spatial relationships. Orthopyroxene is highly deformed, fractured, partially comminuted, and essentially unrecovered. Lamellae of diaplectic glass and other features indicate shock pressures >30 GPa. Bridging acicular crystals and foamy glass at contacts of orthopyroxene fragments indicate localized melting and vaporization of orthopyroxene. Carbonate crystals are >5 mm in size, untwinned, and very largely exhibit the R3c calcite structure. Evidence of plastic deformation is generally found mildly only in fracture‐zone and fracture‐filling carbonates, even adjacent to highly deformed orthopyroxene, and appears to have been caused by low‐stress effects including differential shrinkage. High dislocation densities like those observed in moderately shocked calcite are absent. Carbonate contains impactderived glasses of plagioclase, silica, and orthopyroxene composition indicating brief localized impact heating. Stringers and lenses of orthopyroxene glass in fracture‐filling carbonate imply flow of carbonates and crystallization during an impact. Periclase (MgO) occurs in magnesite as 30–50 nm crystals adjacent to voids and negative crystals and as ?1 μm patches of 3 nm crystals showing weak preferred orientation consistent with (111)_MgO//(0001)_carb, as observed in the thermal decomposition of CaCO₃ to CaO. Magnetite crystals that are epitaxially oriented at voids, negative crystals, and microfractures clearly formed in situ. Fully embedded, faceted magnetites are topotactically oriented, in general with (111)_mag//(0001)_carb, so that their oxygen layers are aligned. In optically opaque rims, magnetites are more irregularly shaped and, except for the smallest crystals, poorly aligned. All magnetite and periclase crystals probably formed by exsolution from slightly non‐stoichiometric, CO₂‐poor carbonate following impact‐induced thermal decomposition. Any magnetites that existed in the rock before shock heating could not have preserved evidence for biogenic activity.     

Olivine in Martian meteorite Allan Hills 84001: Evidence for a high-temperature origin and implications for signs of life

Abstract— Olivine from Martian meteorite Allan Hills (ALH) 84001 occurs as clusters within orthopyroxene adjacent to fractures containing disrupted carbonate globules and feldspathic shock glass. The inclusions are irregular in shape and range in size from ～40 μm to submicrometer. Some of the inclusions are elongate and boudinage-like. The olivine grains are in sharp contact with the enclosing orthopyroxene and often contain small inclusions of chromite. The olivine exhibits a very limited range of composition from Fo₆₅ to Fo₆₆ (n = 25). The δ¹⁸O values of the olivine and orthopyroxene analyzed by ion microprobe range from +4.3 to +5.3‰ and are indistinguishable from each other within analytical uncertainty. The mineral chemistries, O-isotopic data, and textural relationships indicate that the olivine inclusions were produced at a temperature >800 °C. It is unlikely that the olivines formed during the same event that gave rise to the carbonates in ALH 84001, which have more elevated and variable δ¹⁸O values, and were probably formed from fluids that were not in isotopic equilibrium with the orthopyroxene or olivine. The reactions most likely instrumental in the formation of olivine could be either the dehydration of hydrous silicates that formed during carbonate precipitation or the reduction of orthopyroxene and spinel. If the olivine was formed by either reaction during a postcarbonate heating event, the implications are profound with regards to the interpretations of McKay et al. (1996). Due to the low diffusion rates in carbonates, this rapid, high-temperature event would have resulted in the preservation of the fine-scale carbonate zoning, while partially devolatilizing select carbonate compositions on a submicrometer scale (Brearley, 1998a). This may have resulted in the formation of the minute magnetite grains that McKay et al. (1996) attributed to biogenic activity.     

Petrology of Martian meteorite Northwest Africa 998

Abstract— Nakhlite Northwest Africa (NWA) 998 is an augite-rich cumulate igneous rock with mineral compositions and oxygen isotopic composition consistent with an origin on Mars. This 456-gram, partially fusion-crusted meteorite consists of (by volume) ∼75% augite (core composition Wo₃₉En₃₉Fs₂₂), ∼9% olivine (Fo₃₅), ∼7% plagioclase (Ab₆₁An₃₅) as anhedra among augite and olivine, ∼3.5% low-calcium pyroxenes (pigeonite and orthopyroxene) replacing or forming overgrowths on olivine and augite, ∼1% titanomagnetite, and other phases including potassium feldspar, apatite, pyrrhotite, chalcopyrite, ilmenite, and fine-grained mesostasis material. Minor secondary alteration materials include “iddingsite” associated with olivine (probably Martian), calcite crack fillings, and iron oxide/hydroxide staining (both probably terrestrial). Shock effects are limited to minor cataclasis and twinning in augite. In comparison to other nakhlites, NWA 998 contains more low-calcium pyroxenes and its plagioclase crystals are blockier. The large size of the intercumulus feldspars and the chemical homogeneity of the olivine imply relatively slow cooling and chemical equilibration in the late- and post-igneous history of this specimen, and mineral thermometers give subsolidus temperatures near 730 °C. Oxidation state was near that of the QFM buffer, from about QFM-2 in earliest crystallization to near QFM in late crystallization, and to about QFM + 1.5 in some magmatic inclusions. The replacement or overgrowth of olivine by pigeonite and orthopyroxene (with or without titanomagnetite), and the marginal replacement of augite by pigeonite, are interpreted to result from late-stage reactions with residual melts (consistent with experimental phase equilibrium relationships). Apatite is concentrated in planar zones separating apatite-free domains, which suggests that residual magma (rich in P and REE) was concentrated in planar (fracture?) zones and possibly migrated through them. Loss of late magma through these zones is consistent with the low bulk REE content of NWA 998 compared with the calculated REE content of its parent magma.     

USTÍ NAD ORLICI: A NEW L6 CHONDRITE FROM CZECHOSLOVAKIA

Ustí nad Orlici (Kerhartice), a meteorite which fell on June 12, 1963 in Czechoslovakia, is classified as a L6 chondrite. Compositions of olivine (Fa 23.4), orthopyroxene (Fs 20, Wo 1.3), plagioclase (Ab₈₅An₁₀Or₅) along with the bulk composition of the meteorite support this classification. Chromite compositions vary with grain size. Large chromites are higher in TiO₂ and lower in Fe³ than small chromites. This may indicate that either these two chromites formed initially under different fO₂ conditions, or that this difference resulted from different equilibration behaviors of both chromites as a function of grain size. The meteorite contains three distinct sulfide assemblages: 1) troilite-pentlandite, 2) troilite, pentlandite-cubanite-chalcopyrite-pyrrhotite-mackinawite, 3) troilite-tetrataenite-(Fe, Cu, Ni)_{1***. 02}S. These assemblages indicate equilibration down to temperatures close to 200 °C.     

Magmatic inclusions and felsic clasts in the Dar al Gani 319 polymict ureilite

Abstract— Magmatic inclusions occur in type II ureilite clasts (olivine‐orthopyroxene‐augite assemblages with essentially no carbon) and in a large isolated plagioclase clast in the Dar al Gani (DaG) 319 polymict ureilite. Type I ureilite clasts (olivine‐pigeonite assemblages with carbon), as well as other lithic and mineral clasts in this meteorite, are described in Ikeda et al.(2000). The magmatic inclusions in the type II ureilite clasts consist mainly of magnesian augite and glass. They metastably crystallized euhedral pyroxenes, resulting in feldspar component‐enriched glass. On the other hand, the magmatic inclusions in the large plagioclase clast consist mainly of pyroxene and plagioclase, with a mesostasis. They crystallized with a composition along the cotectic line between the pyroxene and plagioclase liquidus fields. DaG 319 also contains felsic lithic clasts that represent various types of igneous lithologies. These are the rare components not found in the common monomict ureilites. Porphyritic felsic clasts, the main type, contain phenocrysts of plagioclase and pyroxene, and their groundmass consists mainly of plagioclase, pyroxene, and minor phosphate, ilmenite, chromite, and/or glass. Crystallization of these porphyritic clasts took place along the cotectic line between the pyroxene and plagioclase fields. Pilotaxitic felsic clasts crystallized plagioclase laths and minor interstitial pyroxene under metastable conditions, and the mesostasis is extremely enriched in plagioclase component in spite of the ubiquitous crystallization of plagioclase laths in the clasts. We suggest that there are two crystallization trends, pyroxene‐metal and pyroxene‐plagioclase trends, for the magmatic inclusions and felsic lithic clasts in DaG 319. The pyroxene‐metal crystallization trend corresponds to the magmatic inclusions in the type II ureilite clasts and the pilotaxitic felsic clasts, where crystallization took place under reducing and metastable conditions, suppressing precipitation of plagioclase. The pyroxene‐plagioclase crystallization trend corresponds to the magmatic inclusions in the isolated plagioclase clast and the porphyritic felsic clasts. This trend developed under oxidizing conditions in magma chambers within the ureilite parent body. The felsic clasts may have formed mainly from albite component‐rich silicate melts produced by fractional partial melting of chondritic precursors. The common monomict ureilites, type I ureilites, may have formed by the fractional partial melting of alkali‐bearing chondritic precursors. However, type II ureilites may have formed as cumulates from a basaltic melt.     

Evidence of shock‐induced vaporization of matrix to form porosity in Baszkówka,a porous L5 chondrite

Baszkówka is an equilibrated, apparently low‐shock, unusually porous chondrite. Some earlier studies were undertaken to understand whether the porosity in Baszkówka, and similar porous chondrites, is a relic of a primordial feature or rather the effect of atypical reprocessing on the parent body. Neither of the studies reconstructed the accurate thermal and deformational evolution of chondrites, however, while it is known that shock‐induced compaction is the main means to affect chondritic porosity. Here we use a combination of 3‐D and 2‐D petrographic examination to understand how the evolution of pores correlates with thermal and shock history recorded in the Baszkówka chondrite. The grain framework silicates in Baszkówka contain healed shock fractures—a clear recorder of significant shock process and postshock annealing. Simultaneously, metal grains do not exhibit any preferred orientation or fabric, which would be expected to develop in response to the deformation as recorded by silicates. We interpret this as evidence for re‐agglomeration and annealing of shocked material. Pore spaces in Baszkówka are connected and decorated by fine‐grained plagioclase‐dominated mass and bulky euhedral olivine crystals, which exhibit growth steps on crystal surfaces. The euhedral olivine must have formed owing to the condensation of a vapor, while plagioclase most likely crystallized from melted chondritic matrix. During the shock event, fine‐grained matrix in Baszkówka was melted and vaporized. Vapor expansion added to ballistic velocity led to ejection and opening of the pore spaces. After re‐agglomeration in a hot ejecta blanket the rock was annealed, melted material circulated in created pore spaces and vapor condensed.     

Shock metamorphism in plagioclase and selective amorphization

Plagioclase feldspar is one of the most common rock‐forming minerals on the surfaces of the Earth and other terrestrial planetary bodies, where it has been exposed to the ubiquitous process of hypervelocity impact. However, the response of plagioclase to shock metamorphism remains poorly understood. In particular, constraining the initiation and progression of shock‐induced amorphization in plagioclase (i.e., conversion to diaplectic glass) would improve our knowledge of how shock progressively deforms plagioclase. In turn, this information would enable plagioclase to be used to evaluate the shock stage of meteorites and terrestrial impactites, whenever they lack traditionally used shock indicator minerals, such as olivine and quartz. Here, we report on an electron backscatter diffraction (EBSD) study of shocked plagioclase grains in a metagranite shatter cone from the central uplift of the Manicouagan impact structure, Canada. Our study suggests that, in plagioclase, shock amorphization is initially localized either within pre‐existing twins or along lamellae, with similar characteristics to planar deformation features (PDFs) but that resemble twins in their periodicity. These lamellae likely represent specific crystallographic planes that undergo preferential structural failure under shock conditions. The orientation of preexisting twin sets that are preferentially amorphized and that of amorphous lamellae is likely favorable with respect to scattering of the local shock wave and corresponds to the “weakest” orientation for a specific shock pressure value. This observation supports a universal formation mechanism for PDFs in silicate minerals.     

Shock and annealing in aubrites: Implications for parent‐body history

Several aubrites (e.g., LAP 03719, Bishopville, Khor Temiki, ALH 83015) contain orthopyroxene grains that exhibit more‐pronounced shock effects than associated olivine grains. The orthopyroxene grains in these samples have clinoenstatite lamellae on (100) and exhibit weak mosaic extinction, characteristic of shock stage S4; the olivine grains exhibit either sharp optical extinction, characteristic of shock stage S1 (as in LAP 03719), or undulose extinction (shock stage S2), as in Bishopville and ALH 83015. The Khor Temiki regolith breccia contains S1 and S2 olivine grains. Because literature data show that diffusion is much slower in orthopyroxene than in olivine, it seems likely that aubrites experienced postshock, impact‐induced annealing. After differentiation, the aubrite parent asteroid suffered major collisions that caused extensive brecciation of near‐surface materials and damaged orthopyroxene and olivine crystal lattices. As a result of these impact events, some aubrites were shocked and buried within warm ejecta blankets or beneath fallback debris under the crater floor. Entombed olivine crystal lattices healed (and became unstrained, reaching shock stage S1), but orthopyroxene lattices retained their S4‐level shock‐damaged features. Aubrites with S4 orthopyroxene and S2 olivine were probably very weakly shocked again after olivine was annealed to S1.     

Complex origins of silicate veinlets in HED meteorites: A case study of Northwest Africa 1109

We report on the petrography and mineralogy of three types of silicate veinlets in the brecciated eucrite Northwest Africa (NWA) 1109. These include Fe‐rich olivine, Mg‐rich olivine, and pyroxene veinlets. The Fe‐rich olivine veinlets mainly infill fractures in pyroxene and also occur along grain boundaries between pyroxene and plagioclase crystals, in both nonequilibrated and equilibrated lithic clasts. The host pyroxene of Fe‐rich olivine veinlets shows large chemical variations between and within grains. The Fe‐rich olivine veinlets also contain fine‐grained Fe³⁺‐bearing chromite, highly calcic plagioclase, merrillite, apatite, and troilite. Based on texture and mineral chemistry, we argue that the formation of Fe‐rich olivine was related to fluid deposition at relatively high temperatures. However, the source of Fe‐rich olivine in the veinlets remains unclear. Magnesium‐rich olivine veinlets were found in three diogenitic lithic clasts. In one of these, the Mg‐rich olivine veinlets only occur in one of the fine‐grained interstitial regions and extend into fractures within surrounding coarse‐grained orthopyroxene. Based on the texture of the interstitial materials, we suggest that the Mg‐rich olivine veinlets formed by shock‐induced localized melting and recrystallization. Pyroxene veinlets were only observed in one clast where they infill fractures within large plagioclase grains and are associated with fine‐grained pyroxene surrounding coarse‐grained pyroxene. The large chemical variations in pyroxene and the fracture‐filling texture indicate that the pyroxene veinlets might also have formed by shock‐induced localized melting and rapid crystallization. Our study demonstrates that silicate veinlets formed by a range of different surface processes on the surface of Vesta.     

Mineralogy of iron sulfides in CM1 and CI1 lithologies of the Kaidun breccia: Records of extreme to intense hydrothermal alteration

The polymict Kaidun microbreccia contains lithologies of C‐type chondrites with euhedral iron sulfide crystals of hydrothermal origin. Our FIB‐TEM study reveals that acicular sulfides in a CM1 lithology are composed of Fe‐rich pyrrhotite with nonintegral vacancy superstructures (NC‐pyrrhotite), troilite, and pentlandite, all showing distinct exsolution textures. Based on phase relations in the Fe‐Ni‐S system, we constrain the temperature of formation of the originally homogeneous monosulfide solid solution to the range of 100–300 °C. In some crystals the exsolution of pentlandite and the microtextural equilibration was incomplete, probably due to rapid cooling. We use thermodynamic modeling to constrain the physicochemical conditions of the extreme hydrothermal alteration in this lithology. Unless the CM1 lithology was sourced from a large depth in the parent body (internal pressure >85 bar) or the temperatures were in the lower range of the interval determined, the water was likely present as vapor. Previously described light δ³⁴S compositions of sulfides in Kaidun's CM1 lithology are likely due to the loss of ³⁴S‐enriched H₂S during boiling. Platy sulfide crystals in an adjacent, intensely altered CI1 lithology are composed of Fe‐poor, monoclinic 4C‐pyrrhotite and NC‐pyrrhotite and probably formed at lower temperatures and higher fS₂ relative to the CM1 lithology. However, a better understanding of the stability of Fe‐poor pyrrhotites at temperatures below 300 °C is required to better constrain these conditions.     

Northwest Africa 428: Impact‐induced annealing of an L6 chondrite breccia

Abstract— Northwest Africa (NWA) 428 is an L chondrite that was successively thermally metamorphosed to petrologic type‐6, shocked to stage S4–S5, brecciated, and annealed to approximately petrologic type‐4. Its thermal and shock history resembles that of the previously studied LL6 chondrite, Miller Range (MIL) 99301, which formed on a different asteroid. The petrologic type‐6 classification of NWA 428 is based on its highly recrystallized texture, coarse metal (150 ± 150 μm), troilite (100 ± 170 μm), and plagioclase (20–60 μm) grains, and relatively homogeneous olivine (Fa_{24.4 ± 0.6}), low‐Ca pyroxene (Fs_{20.5 ± 0.4}), and plagioclase (Ab_{84.2 ± 0.4}) compositions. The petrographic criteria that indicate shock stage S4–S5 include the presence of chromite veinlets, chromite‐plagioclase assemblages, numerous occurrences of metallic Cu, irregular troilite grains within metallic Fe‐Ni, polycrystalline troilite, duplex plessite, metal and troilite veins, large troilite nodules, and low‐Ca clinopyroxene with polysynthetic twins. If the rock had been shocked before thermal metamorphism, low‐Ca clinopyroxene produced by the shock event would have transformed into orthopyroxene. Post‐shock brecciation is indicated by the presence of recrystallized clasts and highly shocked clasts that form sharp boundaries with the host. Post‐shock annealing is indicated by the sharp optical extinction of the olivine grains; during annealing, the damaged olivine crystal lattices healed. If temperatures exceeded those approximating petrologic type‐4 (?600–700°C) during annealing, the low‐Ca clinopyroxene would have transformed into orthopyroxene. The other shock indicators, likewise, survived the mild annealing. An impact event is the most plausible source of post‐metamorphic, post‐shock annealing because any ²⁶Al that may have been present when the asteroid accreted would have decayed away by the time NWA 428 was annealed. The similar inferred histories of NWA 428 (L6) and MIL 99301 (LL6) indicate that impact heating affected more than 1 ordinary chondrite parent body.     

Petrology of silicate inclusions in the Sombrerete ungrouped iron meteorite: Implications for the origins of IIE‐type silicate‐bearing irons

Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo_1–4Fs_25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An_70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.     

Carbonates in fractures of Martian meteorite Allan Hills 84001: Petrologic evidence for impact origin

Abstract— Carbonates in Martian meteorite Allan Hills 84001 occur as grains on pyroxene grain boundaries, in crushed zones, and as disks, veins, and irregularly shaped grains in healed pyroxene fractures. Some carbonate disks have tapered Mg-rich edges and are accompanied by smaller, thinner and relatively homogeneous, magnesite microdisks. Except for the microdisks, all types of carbonate grains show the same unique chemical zoning pattern on MgCO₃-FeCO₃-CaCO₃ plots. This chemical characteristic and the close spatial association of diverse carbonate types show that all carbonates formed by a similar process. The heterogeneous distribution of carbonates in fractures, tapered shapes of some disks, and the localized occurrence of Mg-rich microdisks appear to be incompatible with growth from an externally derived CO₂-rich fluid that changed in composition over time. These features suggest instead that the fractures were closed as carbonates grew from an internally derived fluid and that the microdisks formed from a residual Mg-rich fluid that was squeezed along fractures. Carbonate in pyroxene fractures is most abundant near grains of plagioclase glass that are located on pyroxene grain boundaries and commonly contain major or minor amounts of carbonate. We infer that carbonates in fractures formed from grain boundary carbonates associated with plagioclase that were melted by impact and dispersed into the surrounding fractured pyroxene. Carbonates in fractures, which include those studied by McKay et al. (1996), could not have formed at low temperatures and preserved mineralogical evidence for Martian organisms.     

Shock‐induced phase transformation of anorthitic plagioclase in the eucrite meteorite Northwest Africa 2650

Anorthite is an important constituent mineral in basaltic achondrites from small celestial bodies. Its high‐pressure phase transformation in shocked meteorites has not been systematically studied. In this study, we report the diverse phase transformation behaviors of anorthite in a shocked eucrite Northwest Africa (NWA) 2650, which also contains coesite, stishovite, vacancy‐rich clinopyroxene, super‐silicic garnet, and reidite. Anorthite in NWA 2650 has transformed into anorthite glass (anorthite glassy vein, maskelynite, and glass with a schlieren texture and vesicles), tissintite and dissociated into three‐phase assemblage grossular + kyanite + silica glass. Different occurrences of anorthite glass might have formed via the mechanism involving shear melting, solid‐state transformation, and postshock thermally melting, respectively. Tissintite could have crystallized from a high‐pressure plagioclase melt. The nucleation of tissintite might be facilitated by relict pyroxene fragments and the early formed vacancy‐rich clinopyroxene. The three‐phase assemblage grossular, kyanite, and silica glass should have formed from anorthitic melt at high‐pressure and high‐temperature conditions. The presence of maskelynite and reidite probably suggests a minimum peak shock pressure up to 20 GPa, while the other high‐pressure phases indicate that the shock pressure during the crystallization of shock melt veins might vary from >8 GPa to >2 GPa with a heterogeneous temperature distribution.     

On the formation of diaplectic glass: Shock and thermal experiments with plagioclase of different chemical compositions

This contribution addresses the role of chemical composition, pressure, temperature, and time during the shock transformation of plagioclase into diaplectic glass—i.e., maskelynite. Plagioclase of An_50‐57 and An₉₄ was recovered as almost fully isotropic maskelynite from room temperature shock experiments at 28 and 24 GPa. The refractive index (RI) decreased to values of a quenched mineral glass for An_50‐57 plagioclase shocked to 45 GPa and shows a maximum in An₉₄ plagioclase shocked to 41.5 GPa. The An₉₄ plagioclase experiments can serve as shock thermobarometer for lunar highland rocks and howardite, eucrite, and diogenite meteorites. Shock experiments at 28, 32, 36, and 45 GPa and initial temperatures of 77 and 293 K on plagioclase (An_50‐57) produced materials with identical optical and Raman spectroscopic properties. In the low temperature (<540 K) region, the formation of maskelynite is entirely controlled by shock pressure. The RI of maskelynite decreased in heating experiments of 5 min at temperatures of >770 K, thus, providing a conservative upper limit for the postshock temperature history of the rock. Although shock recovery experiments and static pressure experiments differ by nine orders of magnitude in typical time scale (microseconds versus hours), the amorphization of plagioclase occurs at similar pressure and temperature conditions with both methods. The experimental shock calibration of plagioclase can, together with other minerals, be used as shock thermobarometer for naturally shocked rocks.     

Shock effects in plagioclase feldspar from the Mistastin Lake impact structure,Canada

Shock metamorphism, caused by hypervelocity impact, is a poorly understood process in feldspar due to the complexity of the crystal structure, the relative ease of weathering, and chemical variations, making optical studies of shocked feldspars challenging. Understanding shock metamorphism in feldspars, and plagioclase in particular, is vital for understanding the history of Earth's moon, Mars, and many other planetary bodies. We present here a comprehensive study of shock effects in andesine and labradorite from the Mistastin Lake impact structure, Labrador, Canada. Samples from a range of different settings were studied, from in situ central uplift materials to clasts from various breccias and impact melt rocks. Evidence of shock metamorphism includes undulose extinction, offset twins, kinked twins, alternate twin deformation, and partial to complete transformation to diaplectic plagioclase glass. In some cases, isotropization of alternating twin lamellae was observed. Planar deformation features (PDFs) are notably absent in the plagioclase, even when present in neighboring quartz grains. It is notable that various microlites, twin planes, and compositionally different lamellae could easily be mistaken for PDFs and so care must be taken. A pseudomorphous zeolite phase (levyne‐Ca) was identified as a replacement mineral of diaplectic feldspar glass in some samples, which could, in some instances, also be potentially mistaken for PDFs. We suggest that the lack of PDFs in plagioclase could be due to a combination of structural controls relating to the crystal structure of different feldspars and/or the presence of existing planes of weakness in the form of twin and cleavage planes.     

Petrology of unique achondrite Queen Alexandra Range 93148: A piece of the pallasite (howardite‐eucrite‐diogenite?) parent body?

Abstract— Queen Alexandra Range (QUE) 93148 is a small (1.1 g) olivine‐rich achondrite (mg 86) that contains variable amounts of orthopyroxene (mg 87) and kamacite (6.7 wt% Ni), with minor augite. Olivine in QUE 93148 contains an unusual suite of inclusions: (1) 5 × 100 μm sized lamellae with a CaO‐ and Cr₂O₃‐rich (～10 and 22 wt%, respectively) composition that may represent a submicrometer‐scale intergrowth of chromite and pyroxene(s); (2) 75 × 500 μm sized lamellar symplectites composed of chromite and two pyroxenes, with minor metal; (3) 15–20 μm sized, irregularly‐shaped symplectites composed of chromite and pyroxene(s); (4) 100–150 μm sized, elliptical inclusions composed of chromite, two pyroxenes, metal, troilite, and rare whitlockite. Type 1, 2, and 3 inclusions probably formed by exsolution from the host olivine during slow cooling, whereas type 4 more likely resulted from early entrapment of silicate and metallic melts followed by closed‐system oxidation. Queen Alexandra Range 93148 can be distinguished from most other olivine‐rich achondrites (ureilites, winonaites, lodranites, acapulcoites, brachinites, Eagle‐Station‐type pallasites, and pyroxene pallasites), as well as from mesosiderites, by some or all of the following properties: O‐isotopic composition, Fe‐Mn‐Mg relations of olivine, CaO and Cr₂O₃ contents of olivine, orthopyroxene compositions, molar Cr/(Cr + Al) ratios of chromite, metal composition, texture, and the presence of the inclusions. In terms of many of these properties, it shows an affinity to main‐group pallasites. Nevertheless, it cannot be identified as belonging to this group. Meteorite QUE 93148 appears to be a unique achondrite. Possibly it should be considered to be a pyroxene pallasite that is genetically related to main‐group pallasites. Alternatively, it may be derived from the mantle of the pallasite (howardite‐eucrite‐diogenite?) parent body.     

Multi‐generational carbonate assemblages in martian meteorite Allan Hills 84001: Implications for nucleation,growth, and alteration

Abstract— The carbonate mineralogy of several complex carbonate‐rich regions in Allan Hills (ALH) 84001 has been examined. These regions contain familiar forms of carbonate, as well as textural forms previously unreported including carbonate rosettes, planiform “slab” carbonates, distinct “post‐slab” magnesites, and carbonates interstitial to feldspathic glass and orthopyroxene. Slab carbonates reveal portions of the carbonate growth sequence not seen in the rosettes and suggest that initial nucleating compositions were calcite‐rich. The kinetically controlled growth of rosettes and slab carbonates was followed by an alteration event that formed the magnesite‐siderite layers on the exterior surfaces of the carbonate. Post‐slab magnesite, intimately associated with silica glass, is compositionally similar to the magnesite in these exterior layers but represents a later generation of carbonate growth. Feldspathic glasses had little or no thermal effect on carbonates, as indicated by the lack of thermal decomposition or any compositional changes associated with glass/carbonate contacts.