High‐pressure polymorphs of magnesian orthopyroxene from a shock vein in the Yamato‐000047 lherzolitic shergottite

Abstract– We found a simple thin shock vein, less than or equal to about 60 μm in width and 1.8 mm in length, in the poikilitic area in the Yamato (Y‐) 000047 lherzolitic shergottite. The shock vein occurs only in magnesian Ca‐poor clinopyroxene, which may have transformed from orthopyroxene during the pressure increase at the shock event. The shock vein consists of (Mg_0.8,Fe_0.2)SiO₃ pyroxene polymorphs, such as columnar akimotoite, two kinds of pyroxene glasses, dendritic akimotoite, and framboidal pyroxene glass, in the order from the periphery to the center. The compositions and textures suggest that columnar akimotoite in the periphery of the shock vein crystallized from solid‐state phase transition of clinopyoroxene during the cooling of the vein, and the remains in the shock vein solidified from shock‐produced melt. The glass includes two kinds of massive glass in the vein and framboidal glass in the vein center. The framboidal glass is the most magnesian and may have been vitrified from perovskite crystallized from high‐pressure melt produced at high temperature ≥3000 °C and high‐pressure 23–40 GPa. Dendritic akimotoites in the vein center metastably crystallized from residual shock melt. The formation sequences of the constituent phases in the shock vein happen in the following order: columnar akimotoites, rim glass, center glass, framboidal glass, and dendritic akimotoites. The increase of the Raman intensity of 660–670 cm^?1 in the order of rim glass, center glass, and framboidal glass suggests that the formation of the pyroxene chain proceeds faster in the vein center than in the vein rim due to its slower cooling. The finding of the shock vein consisting merely of high‐pressure polymorphs of pyroxene, akimotoite, and framboidal glass (vitrified perovskite) is the first reported among all Martian meteorites.     

Estimating shock pressures based on high‐pressure minerals in shock‐induced melt veins of L chondrites

Abstract— Here we report the transmission electron microscopy (TEM) observations of the mineral assemblages and textures in shock‐induced melt veins from seven L chondrites of shock stages ranging from S3 to S6. The mineral assemblages combined with phase equilibrium data are used to constrain the crystallization pressures, which can be used to constrain shock pressure in some cases. Thick melt veins in the Tenham L6 chondrite contain majorite and magnesiowüstite in the center, and ringwoodite, akimotoite, vitrified silicate‐perovskite, and majorite in the edge of the vein, indicating crystallization pressure of ?25 GPa. However, very thin melt veins (5–30 μm wide) in Tenham contain glass, olivine, clinopyroxene, and ringwoodite, suggesting crystallization during transient low‐pressure excursions as the shock pressure equilibrated to a continuum level. Melt veins of Umbarger include ringwoodite, akimotoite, and clinopyroxene in the vein matrix, and Fe₂SiO₄‐spinel and stishovite in SiO₂‐FeO‐rich melt, indicating a crystallization pressure of ?18 GPa. The silicate melt veins in Roy contain majorite plus ringwoodite, indicating pressure of ?20 GPa. Melt veins of Ramsdorf and Nakhon Pathon contain olivine and clinoenstatite, indicating pressure of less than 15 GPa. Melt veins of Kunashak and La Lande include albite and olivine, indicating crystallization at less than 2.5 GPa. Based upon the assemblages observed, crystallization of shock veins can occur before, during, or after pressure release. When the assemblage consists of high‐pressure minerals and that assemblage is constant across a larger melt vein or pocket, the crystallization pressure represents the equilibrium shock pressure.     

New observations on high‐pressure phases in a shock melt vein in the Villalbeto de la Peña meteorite: Insights into the shock behavior of diopside

The petrology and mineralogy of shock melt veins in the L6 ordinary chondrite host of Villalbeto de la Peña, a highly shocked, L chondrite polymict breccia, have been investigated in detail using scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and electron probe microanalysis. Entrained olivine, enstatite, diopside, and plagioclase are transformed into ringwoodite, low‐Ca majorite, high‐Ca majorite, and an assemblage of jadeite‐lingunite, respectively, in several shock melt veins and pockets. We have focused on the shock behavior of diopside in a particularly large shock melt vein (10 mm long and up to 4 mm wide) in order to provide additional insights into its high‐pressure polymorphic phase transformation mechanisms. We report the first evidence of diopside undergoing shock‐induced melting, and the occurrence of natural Ca‐majorite formed by solid‐state transformation from diopside. Magnesiowüstite has also been found as veins injected into diopside in the form of nanocrystalline grains that crystallized from a melt and also occurs interstitially between majorite‐pyrope grains in the melt‐vein matrix. In addition, we have observed compositional zoning in majorite‐pyrope grains in the matrix of the shock‐melt vein, which has not been described previously in any shocked meteorite. Collectively, all these different lines of evidence are suggestive of a major shock event with high cooling rates. The minimum peak shock conditions are difficult to constrain, because of the uncertainties in applying experimentally determined high‐pressure phase equilibria to complex natural systems. However, our results suggest that conditions between 16 and 28 GPa and 2000–2200 °C were reached.     

Petrogenesis and shock metamorphism of the enriched lherzolitic shergottite Northwest Africa 7755

Northwest Africa (NWA) 7755 is a newly found enriched lherzolitic shergottite. Here, we report its detailed petrography and mineralogy. NWA 7755 contains both poikilitic and non‐poikilitic lithologies. Olivine has different compositional ranges in the poikilitic and non‐poikilitic lithologies, Fa_30–39 and Fa_37–40, respectively. Pyroxene in the non‐poikilitic lithology is systematically Fe‐richer than that in the poikilitic lithology. The chromite grains in non‐poikilitic lithology are highly Ti‐richer than those in the poikilitic lithology. The chemical variations of olivine, pyroxene, and chromite between the poikilitic and non‐poikilitic lithologies support a two‐stage formation model of lherzolitic shergottites. Besides planar fractures and strong mosaicism in olivine and pyroxene, shock‐induced melt veins and pockets are observed in NWA 7755. Olivine grains within and adjacent to melt veins and/or pockets have either transformed to ringwoodite, amorphous phase, or dissociated to bridgmanite plus magnesiowüstite. Merrillite in melt veins has completely transformed to tuite; however, apatite only has partially transformed to tuite, indicating a relatively sluggish transformation rate. The partial transformation from apatite to tuite resulted in fractional devolatilization of Cl and F in apatite. The fine‐grained mineral assemblage in melt veins consists mainly of bridgmanite, minor magnesiowüstite, Fe‐sulfide, Fe‐phosphide, and Ca‐phosphate minerals. The coexistence of bridgmanite and magnesiowüstite in these veins indicates a shock pressure of >~24 GPa and a temperature of 1800–2000 °C. Coesite and seifertite are probably present in NWA 7755. The presence of these high‐pressure minerals indicates that NWA 7755 has experienced a more intense shock metamorphism than other enriched lherzolitic shergottites.     

A large shock vein in L chondrite Roosevelt County 106: Evidence for a long‐duration shock pulse on the L chondrite parent body

A large shock‐induced melt vein in L6 ordinary chondrite Roosevelt County 106 contains abundant high‐pressure minerals, including olivine, enstatite, and plagioclase fragments that have been transformed to polycrystalline ringwoodite, majorite, lingunite, and jadeite. The host chondrite at the melt‐vein margins contains olivines that are partially transformed to ringwoodite. The quenched silicate melt in the shock veins consists of majoritic garnets, up to 25 μm in size, magnetite, maghemite, and phyllosilicates. The magnetite, maghemite, and phyllosilicates are the terrestrial alteration products of magnesiowüstite and quenched glass. This assemblage indicates crystallization of the silicate melt at approximately 20–25 GPa and 2000 °C. Coarse majorite garnets in the centers of shock veins grade into increasingly finer grained dendritic garnets toward the vein margins, indicating increasing quench rates toward the margins as a result of thermal conduction to the surrounding chondrite host. Nanocrystalline boundary zones, that contain wadsleyite, ringwoodite, majorite, and magnesiowüstite, occur along shock‐vein margins. These zones represent rapid quench of a boundary melt that contains less metal‐sulfide than the bulk shock vein. One‐dimensional finite element heat‐flow calculations were performed to estimate a quench time of 750–1900 ms for a 1.6‐mm thick shock vein. Because the vein crystallized as a single high‐pressure assemblage, the shock pulse duration was at least as long as the quench time and therefore the sample remained at 20–25 GPa for at least 750 ms. This relatively long shock pulse, combined with a modest shock pressure, implies that this sample came from deep in the L chondrite parent body during a collision with a large impacting body, such as the impact event that disrupted the L chondrite parent body 470 Myr ago.     

Transformation textures,mechanisms of formation of high‐pressure minerals in shock melt veins of L6 chondrites,and pressure‐temperature conditions of the shock events

Abstract— The high‐pressure polymorphs of olivine, pyroxene, and plagioclase in or adjacent to shock melt veins (SMVs) in two L6 chondrites (Sahara 98222 and Yamato 74445) were investigated to clarify the related transformation mechanisms and to estimate the pressure‐temperature conditions of the shock events. Wadsleyite and jadeite were identified in Sahara 98222. Wadsleyite, ringwoodite, majorite, akimotoite, jadeite, and lingunite (NaAlSi₃O₈‐hollandite) were identified in Yamato 74445. Wadsleyite nucleated along the grain boundaries and fractures of original olivine. The nucleation and growth of ringwoodite occurred along the grain boundaries of original olivine, and as intracrystalline ringwoodite lamellae within original olivine. The nucleation and growth of majorite took place along the grain boundaries or fractures in original enstatite. Jadeite‐containing assemblages have complicated textures containing “particle‐like,” “stringer‐like,” and “polycrystalline‐like” phases. Coexistence of lingunite and jadeite‐containing assemblages shows a vein‐like texture. We discuss these transformation mechanisms based on our textural observations and chemical composition analyses. The shock pressure and temperature conditions in the SMVs of these meteorites were also estimated based on the mineral assemblages in the SMVs and in comparison with static high‐pressure experimental results as follows: 13–16 GPa, >1900 °C for Sahara 98222 and 17–24 GPa, >2100 °C for Yamato 74445.     

Petrology and Raman spectroscopy of high pressure phases in the Gujba CB chondrite and the shock history of the CB parent body

Abstract– High pressure phases majorite, possibly majorite‐pyrope_ss, wadsleyite, and coesite are present in the matrix and in barred olivine fragments in the Gujba CB chondrite. Grossular‐pyrope was also observed in some small inclusions. The CB chondrites are metal‐rich meteorites with characteristics that sharply distinguish them from other chondrite groups. All of the CB chondrites contain impact melt regions interstitial to their chondrules, fragments and metal and a major impact event (or events), on the CB chondrite parent body is clearly a significant stage in its history. We studied three areas interstitial to chondrules and metal in the Gujba CB_a chondrite. From Raman spectra, the barred olivine fragments and matrix in these regions have various combinations of olivine and low‐Ca pyroxene, as well as majorite garnet (Mg₄Si₄O₁₂), a phase that forms by high‐pressure transformation of low‐Ca pyroxene and wadsleyite, a high pressure product of olivine. Compositions of the majorite suggest both majorite and majorite‐pyrope solid solution may be present. The mineral assemblage of majorite and wadsleyite suggest minimum shock pressures and temperatures of ～19 GPa and ～2000 °C, respectively. The occurrences of high pressure phases are variable from one area to another, on the scale of millimeters or less, suggesting heterogeneous distribution of shock and/or back transformation to low pressure polymorphs throughout the meteorite. The high pressure phases record a high temperature–pressure impact event that is superimposed onto, and thus postdates formation of, the chondrules and other components in the CB chondrites. The barred chondrules and metal in the CB chondrites are primary materials formed prior to the impact event either generated in an earlier planetesimal scale impact event or in the nebula.     

Mechanisms of ringwoodite formation in shocked meteorites: Evidence from L5 chondrite Dhofar 1970

The formation of the high‐pressure compositional equivalents of olivine and pyroxene has been well‐documented within and surrounding shock‐induced veins in chondritic meteorites, formed by crystallization from a liquid‐ or solid‐state phase transformation. Typically polycrystalline ringwoodite grains have a narrow range of compositions that overlap with those of their olivine precursors, whereas the formation of iron‐enriched ringwoodite has been documented from only a handful of meteorites. Here, we report backscattered electron images, quantitative wavelength‐dispersive spectrometry (WDS) analyses, qualitative WDS elemental X‐ray maps, and micro‐Raman spectra that reveal the presence of Fe‐rich ringwoodite (Fa_44‐63) as fine‐grained (500 nm), polycrystalline rims on olivine (Fa_24‐25) wall rock and as clasts engulfed by shock melt in a previously unstudied L5 chondrite, Dhofar 1970. Crystallization of majorite + magnesiowüstite in the vein interior and metastable mineral assemblages within 35 μm of the vein margin attest to rapid crystallization of a superheated shock melt (>2300 K) from 20─25 GPa to ambient pressure and temperature. The texture and composition of bright polycrystalline ringwoodite rims (Fa_44‐63; MnO 0.01─0.08 wt%) surrounding dark polycrystalline olivine (Fa_8‐14; MnO 0.56─0.65 wt%) implies a solid‐state transformation mechanism in which Fe was preferentially partitioned to ringwoodite. The spatial association between ringwoodite and shock melt suggests that the rapidly fluctuating thermal regimes experienced by chondritic minerals in contact with shock melt are necessary to both drive phase transformation but also to prevent back‐transformation.     

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.     

Shock and annealing in the amphibole‐ and mica‐bearing R chondrites

MIL 11207 (R6) and LAP 04840 (R6) contain hornblende and phlogopite; MIL 07440 (R6) contains accessory titan‐phlogopite and no hornblende. All three meteorites have been shocked: MIL 11207 contains extensive sulfide veins, pyroxene that formed from dehydrated hornblende, and an extensive network of plagioclase glass; MIL 07440 contains chromite‐plagioclase assemblages, chromite veinlets and blebs, pincer‐shaped plagioclase patches, but no sulfide veins; LAP 04840 contains olivine grains with chromite‐bleb‐laden cores and opaque‐free rims, rare grains of pyroxene that formed from dehydrated hornblende, and no sulfide veins. These meteorites appear to have been heated to maximum temperatures of approximately 700–900 °C under conditions of moderately high PH₂O (perhaps 250–500 bars). All three samples underwent postshock annealing. During this process, olivine crystal lattices healed (giving the rocks the appearance of shock‐stage S1), and diffusion of Fe and S from thin sulfide veins to coarse sulfide grains caused the veins to disappear in MIL 07440 and LAP 04840. This latter process apparently also occurred in most S1–S2 ordinary chondrites of high petrologic type. The pressure–temperature conditions responsible for forming the amphibole and mica in these rocks may have been present at depths of a few tens of kilometers (as suggested in the literature). A giant impact or a series of smaller impacts would then have been required to excavate the hornblende‐ and biotite‐bearing rocks and bring them closer to the surface. It was in that latter location where the samples were shocked, deposited in a hot ejecta blanket of low thermal diffusivity, and annealed.     

Impact melting of lunar meteorite Dhofar 458: Evidence from polycrystalline texture and decomposition of zircon

Abstract– Dhofar 458 is a lunar meteorite consisting mainly of olivine‐plagioclase intergrowths, pyroxene‐plagioclase intergrowths, and plagioclase fragments. Pyroxene‐plagioclase globules are also common. In this study, we report the discovery of a polycrystalline zircon in this lunar meteorite. The polycrystalline zircon contains small vesicles and rounded baddeleyite grains at its margin. The polycrystalline and porous texture of the zircon indicates high‐pressure shock‐induced melting and degassing. Baddeleyite grains are derived from decomposition of zircon under high postshock temperature. The shock features in zircon indicates that the shock pressure in Dhofar 458 was greater than approximately 60 GPa and the postshock temperature greater than approximately 1700 °C. The polycrystalline and degassing texture and decomposition zircon also strongly indicates that Dhofar 458 is a clast‐rich impact melt rock. During this shock event, most components were melted and grains of mafic minerals are interstitial to lath‐like plagioclase grains. Large fragments of olivine and chromite also formed polycrystalline texture at margins and chemically reequilibrated with surrounding melts. We suggest that pyroxene‐plagioclase globules could be remains of melted target clasts, whereas vesicles may form during shock‐induced degassing of the rock. The U‐Pb isotopic data plot on a well‐defined discordant line, yielding the age of the zircon of 3434 ± 15 Ma (2σ). This age is interpreted as the time of the impact event that melted Dhofar 458 and caused decomposition and recrystallization of this zircon in Dhofar 458, which reset this zircon’s U‐Pb age.     

Two distinct assemblages of high‐pressure liquidus phases in shock veins of the Sixiangkou meteorite

Abstract— Shock‐produced complex veins, including earlier and later veins, are identified in the Sixiangkou L6 chondrite. The early vein is intersected by the late vein and consists of coarse‐grained aggregates of ringwoodite, majorite, and lingunite, and fragments of olivine, pyroxene, plagioclase, metal, and troilite, as well as a fine‐grained matrix of garnet, ringwoodite, metal, and troilite. The late vein mainly consists of a fine‐grained matrix of garnet, magnesiowüstite, metal, and troilite, as well as a small amount of coarse‐grained aggregates. The amount of fine‐grained matrix suggests that the late vein was nearly completely melted, whereas the early vein underwent partial melting. Both fine‐grained assemblages of garnet plus ringwoodite in the early vein and garnet plus magnesiowüstite in the late vein are liquidus phases crystallized from shock‐induced melt. Based on our understanding of the liquidus assemblages, the late vein experienced a higher pressure and temperature than the early vein.     

Redistribution of elements in the heavily shocked Yanzhuang chondrite

Abstract— Compositions of metal, sulfide, olivine, pyroxene, and plagioclase/plagioclase glass were studied for the melted and unmelted parts of the heavily shocked H6(S6) chondrite‐Yanzhuang. We found that the partitioning of some trace elements significantly changed between the 2 parts; compared with the corresponding minerals in the unmelted part, Ga is enriched in the metal, Co, Cr, and Zn are enriched in the sulfide, Cr is enriched in olivine and pyroxene, and Ti is enriched in the plagioclase glass of the melt pocket. These detailed studies of the mineral phases put constraints on 3 important parameters (temperature, pressure, and duration) associated with the post‐shock melting process. The coexistence of melted and unmelted olivine in the melt pocket of Yanzhuang implies a peak temperature after shock that approaches the melting point of olivine. The lack of Ni in the olivine crystallized from a melt suggests crystallization of olivine at pressures below 10 kbar. The resetting of Ga partitioning between metal and silicate in the melt pocket indicates that the interval from the peak temperature after shock to the crystallization of metal‐sulfide and plagioclase glass in the melted part of Yanzhuang is longer than 500 sec.     

Refractory calcium‐aluminum‐rich inclusions and aluminum‐diopside‐rich chondrules in the metal‐rich chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94411

Abstract— The metal‐rich chondrites Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627, contain relatively rare (<1 vol%) calcium‐aluminum‐rich inclusions (CAIs) and Al‐diopside‐rich chondrules. Forty CAIs and CAI fragments and seven Al‐diopside‐rich chondrules were identified in HH 237 and QUE 94411/94627. The CAIs, ～50–400 μm in apparent diameter, include (a) 22 (56%) pyroxene‐spinel ± melilite (+forsterite rim), (b) 11 (28%) forsterite‐bearing, pyroxene‐spinel ± melilite ± anorthite (+forsterite rim) (c) 2 (5%) grossite‐rich (+spinel‐melilite‐pyroxene rim), (d) 2 (5%) hibonite‐melilite (+spinel‐pyroxene ± forsterite rim), (e) 1 (2%) hibonite‐bearing, spinel‐perovskite (+melilite‐pyroxene rim), (f) 1 (2%) spinel‐melilite‐pyroxene‐anorthite, and (g) 1 (2%) amoeboid olivine aggregate. Each type of CAI is known to exist in other chondrite groups, but the high abundance of pyroxene‐spinel ± melilite CAIs with igneous textures and surrounded by a forsterite rim are unique features of HH 237 and QUE 94411/94627. Additionally, oxygen isotopes consistently show relatively heavy compositions with Δ¹⁷O ranging from ?6%0 to ?10%0 (1σ = 1.3%0) for all analyzed CAI minerals (grossite, hibonite, melilite, pyroxene, spinel). This suggests that the CAIs formed in a reservoir isotopically distinct from the reservoir(s) where “normal”, ¹⁶O‐rich (Δ¹⁷O < ?20%0) CAIs in most other chondritic meteorites formed. The Al‐diopside‐rich chondrules, which have previously been observed in CH chondrites and the unique carbonaceous chondrite Adelaide, contain Al‐diopside grains enclosing oriented inclusions of forsterite, and interstitial anorthitic mesostasis and Al‐rich, Ca‐poor pyroxene, occasionally enclosing spinel and forsterite. These chondrules are mineralogically similar to the Al‐rich barred‐olivine chondrules in HH 237 and QUE 94411/94627, but have lower Cr concentrations than the latter, indicating that they may have formed during the same chondrule‐forming event, but at slightly different ambient nebular temperatures. Aluminum‐diopside grains from two Al‐diopside‐rich chondrules have O‐isotopic compositions (Δ¹⁷O ? ?7 ± 1.1 %0) similar to CAI minerals, suggesting that they formed from an isotopically similar reservoir. The oxygen‐isotopic composition of one Ca, Al‐poor cryptocrystalline chondrule in QUE 94411/94627 was analyzed and found to have Δ¹⁷O ? ?3 ± 1.4%0. The characteristics of the CAIs in HH 237 and QUE 94411/94627 are inconsistent with an impact origin of these metal‐rich meteorites. Instead they suggest that the components in CB chondrites are pristine products of large‐scale, high‐temperature processes in the solar nebula and should be considered bona fide chondrites.     

A vacancy‐rich,partially inverted spinelloid silicate, (Mg,Fe,Si)2(Si,□)O4, as a major matrix phase in shock melt veins of the Tenham and Suizhou L6 chondrites

A new high‐pressure silicate, (Mg,Fe,Si)₂(Si,□)O₄ with a tetragonal spinelloid structure, was discovered within shock melt veins in the Tenham and Suizhou meteorites, two highly shocked L6 ordinary chondrites. Relative to ringwoodite, this phase exhibits an inversion of Si coupled with intrinsic vacancies and a consequent reduction of symmetry. Most notably, the spinelloid makes up about 30–40 vol% of the matrix of shock veins with the remainder composed of a vitrified (Mg,Fe)SiO₃ phase (in Tenham) or (Mg,Fe)SiO₃‐rich clinopyroxene (in Suizhou); these phase assemblages constitute the bulk of the matrix in the shock veins. Previous assessments of the melt matrices concluded that majorite and akimotoite were the major phases. Our contrasting result requires revision of inferred conditions during shock melt cooling of the Tenham and Suizhou meteorites, revealing in particular a much higher quench rate (at least 5 × 10³ K s^?1) for veins of 100–500 μm diameter, thus overriding formation of the stable phase assemblage majoritic garnet plus periclase.     

Silica as a shock index in shergottites: A cathodoluminescence study

Abstract— Silica in shergottites is a minor phase of great significance. Determining its structural state as either silica glass, quartz, cristobalite, tridymite, coesite, stishovite, or post‐stishovite could provide informations about their shock history. The purpose of this work is to assess the shock intensity in shergottites using two spectroscopic methods. On a conventional polished section, a scanning electron microscope (SEM) enables us to study the cathodoluminescence (CL) of silica at variable magnification. The results were crosschecked by systematic Raman spectroscopy of the selected areas. CL spectra differ substantially from one another and enable separating stishovite, high and low pressure silica glass, quartz, and cristobalite. We studied a set of five shergottites: Northwest Africa (NWA) 480, NWA 856, Zagami, Shergotty, and Los Angeles. Stishovite is common in Shergotty, Zagami, NWA 856, and NWA 480 and absent in the studied section of Los Angeles. High‐pressure glass is very common, particularly in close association with stishovite. According to the textural relationship, it may be a product of the retromorphosis (amorphization during decompression) of stishovite. Large stishovite areas result from the transformation of preexisting low‐pressure silica crystals, while needles result from the high‐pressure transformation of pyroxene to glass (melt) and silica. In the latter case, they are found in melt pockets and represent a small fraction of areas of overall pyroxene composition. Needles exhibit square sections of about 1 μm. Silica spots identical to those described previously as post‐stishovite are found in Shergotty, Zagami, NWA 480, and NWA 856. At present, the spectroscopic distinction of post‐stishovite from stishovite is difficult. Post‐stishovite is destroyed under the Raman beam, and CL spectra are possible mixtures of several phases (e.g., glass and post‐stishovite). It is concluded that the shock intensity is highly heterogeneous, and the pressure probably exceeded 60 GPa in all shergottites studied here.     

Mineralogy,petrology, and shock history of lunar meteorite Sayh al Uhaymir 300: A crystalline impact‐melt breccia

Abstract— Sayh al Uhaymir (SaU) 300 comprises a microcrystalline igneous matrix (grain size <10 μm), dominated by plagioclase, pyroxene, and olivine. Pyroxene geothermometry indicates that the matrix crystallized at ?1100 °C. The matrix encloses mineral and lithic clasts that record the effects of variable levels of shock. Mineral clasts include plagioclase, low‐ and high‐Ca pyroxene, pigeonite, and olivine. Minor amounts of ilmenite, FeNi metal, chromite, and a silica phase are also present. A variety of lithic clast types are observed, including glassy impact melts, impact‐melt breccias, and metamorphosed impact melts. One clast of granulitic breccia was also noted. A lunar origin for SaU 300 is supported by the composition of the plagioclase (average An₉₅), the high Cr content in olivine, the lack of hydrous phases, and the Fe/Mn ratio of mafic minerals. Both matrix and clasts have been locally overprinted by shock veins and melt pockets. SaU 300 has previously been described as an anorthositic regolith breccia with basaltic components and a granulitic matrix, but we here interpret it to be a polymict crystalline impact‐melt breccia with an olivine‐rich anorthositic norite bulk composition. The varying shock states of the mineral and lithic clasts suggest that they were shocked to between 5–28 GPa (shock stages S1–S2) by impact events in target rocks prior to their inclusion in the matrix. Formation of the igneous matrix requires a minimum shock pressure of 60 GPa (shock stage >S4). The association of maskelynite with melt pockets and shock veins indicates a subsequent, local 28–45 GPa (shock stage S2–S3) excursion, which was probably responsible for lofting the sample from the lunar surface. Subsequent fracturing is attributed to atmospheric entry and probable breakup of the parent meteor.     

The distinct morphological and petrological features of shock melt veins in the Suizhou L6 chondrite

Abstract– The morphology and petrology of distinct melt veins in the Suizhou L6 chondrite have been investigated using scanning electron microscopy, electron microprobe analyses, and Raman spectroscopy, synchrotron energy‐dispersive diffraction, and transmission electron microscopy. It is found that the melt veins in the Suizhou meteorite morphologically are the simplest, straightest, and thinnest among all shock veins known from meteorites. At first glance, these veins look like fine fractures, but petrologically they are solid melt veins of chondritic composition and consist of fully crystalline materials of two distinct lithological assemblages, with no glassy material remaining. The Suizhou melt veins contain the most abundant high‐pressure mineral species when compared with all other veins known in chondrites. Thus, these veins in Suizhou are classified as shock veins. All rock‐forming and almost all accessory minerals in the Suizhou shock veins have been transformed to their high‐pressure polymorphs, and no fragments of the precursor minerals remain in the veins. Among the 11 high‐pressure mineral phases identified in the Suizhou veins, three are new high‐pressure minerals, namely, tuite after whitlockite, xieite, and the CF phase after chromite. On the basis of transformation of plagioclase into maskelynite, it is estimated that the Suizhou meteorite experienced shock pressures and shock temperatures up to 22 GPa and 1000 °C, respectively. Shearing and friction along shock veins raised the temperature up to 1900–2000 °C and the pressure up to 24 GPa within the veins. Hence, phase transition and crystallization of high‐pressure minerals took place only in the Suizhou shock veins. Fast cooling of the extremely thin shock veins is regarded as the main reason that up to 11 shock‐induced high‐pressure mineral phases could be preserved in these veins.     

HAVERÖ UREILITE: EVIDENCE FOR RECRYSTALLIZATION AND PARTIAL REDUCTION

Haverö consists of large olivine areas with a pavement structure and single crystals of twinned clinopyroxene. Black veins with sharp boundaries traverse the silicates. They contain graphite, diamond, and kamacite. In olivine a reaction rim is formed around these veins containing Ni-poor metal and showing a lower FeO content than farther away from the vein. The CaO content of olivine and pyroxene, 0.27% and 1.7%, respectively, are higher than in these minerals in normal chondrites. The mole percent Fe + Ca/Fe + Ca + Mg in unchanged olivine and in pyroxene agree with the range of L-chondrites. Metal occurs in three types: a, larger grains in the course of the black veins, they contain 2 to 3% Ni; b, micron-sized grains inside the black veins and its reaction rim; c, medium-sized grains with ～0.7% Ni in olivine The interpretation of these observations is: a material similar to an L-chondrite was reheated and recrystallized (at this time it may have lost its feldspar, metal and troilite by partial melting), Ca was redistributed and partly retained in olivine and pyroxene due to rapid cooling, a late introduction of carbon into veins caused a partial reduction of FeO in olivine and formation of Ni-poor metal     

Spade: An H chondrite impact‐melt breccia that experienced post‐shock annealing

Abstract— The low modal abundances of relict chondrules (1.8 vol%) and of coarse (i.e., ≥200 μm‐size) isolated mafic silicate grains (1.8 vol%) in Spade relative to mean H6 chondrites (11.4 and 9.8 vol%, respectively) show Spade to be a rock that has experienced a significant degree of melting. Various petrographic features (e.g., chromite‐plagioclase assemblages, chromite veinlets, silicate darkening) indicate that melting was caused by shock. Plagioclase was melted during the shock event and flowed so that it partially to completely surrounded nearby mafic silicate grains. During crystallization, plagioclase developed igneous zoning. Low‐Ca pyroxene that crystallized from the melt (or equilibrated with the melt at high temperatures) acquired relatively high amounts of CaO. Metallic Fe‐Ni cooled rapidly below the Fe‐Ni solvus and transformed into martensite. Subsequent reheating of the rock caused transformation of martensite into abundant duplex plessite. Ambiguities exist in the shock stage assignment of Spade. The extensive silicate darkening, the occurrence of chromite‐plagioclase assemblages, and the impact‐melted characteristics of Spade are consistent with shock stage S6. Low shock (stage S2) is indicated by the undulose extinction and lack of planar fractures in olivine. This suggests that Spade reached a maximum prior shock level equivalent to stage S6 and then experienced post‐shock annealing (probably to stage S1). These events were followed by a less intense impact that produced the undulose extinction in the olivine, characteristic of shock stage S2. Annealing could have occurred if Spade were emplaced near impact melts beneath the crater floor or deposited in close proximity to hot debris within an ejecta blanket. Spade firmly establishes the case for post‐shock annealing. This may have been a common process on OC asteroids.