High‐pressure minerals in shocked meteorites

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

Hydrogen isotopic composition of the Martian mantle inferred from the newest Martian meteorite fall,Tissint

The hydrogen isotopic composition of planetary reservoirs can provide key constraints on the origin and history of water on planets. The sources of water and the hydrological evolution of Mars may be inferred from the hydrogen isotopic compositions of mineral phases in Martian meteorites, which are currently the only samples of Mars available for Earth‐based laboratory investigations. Previous studies have shown that δD values in minerals in the Martian meteorites span a large range of ?250 to +6000‰. The highest hydrogen isotope ratios likely represent a Martian atmospheric component: either interaction with a reservoir in equilibrium with the Martian atmosphere (such as crustal water), or direct incorporation of the Martian atmosphere due to shock processes. The lowest δD values may represent those of the Martian mantle, but it has also been suggested that these values may represent terrestrial contamination in Martian meteorites. Here we report the hydrogen isotopic compositions and water contents of a variety of phases (merrillites, maskelynites, olivines, and an olivine‐hosted melt inclusion) in Tissint, the latest Martian meteorite fall that was minimally exposed to the terrestrial environment. We compared traditional sample preparation techniques with anhydrous sample preparation methods, to evaluate their effects on hydrogen isotopes, and find that for severely shocked meteorites like Tissint, the traditional sample preparation techniques increase water content and alter the D/H ratios toward more terrestrial‐like values. In the anhydrously prepared Tissint sample, we see a large range of δD values, most likely resulting from a combination of processes including magmatic degassing, secondary alteration by crustal fluids, shock‐related fractionation, and implantation of Martian atmosphere. Based on these data, our best estimate of the δD value for the Martian depleted mantle is ?116 ± 94‰, which is the lowest value measured in a phase in the anhydrously prepared section of Tissint. This value is similar to that of the terrestrial upper mantle, suggesting that water on Mars and Earth was derived from similar sources. The water contents of phases in Tissint are highly variable, and have been affected by secondary processes. Considering the H₂O abundances reported here in the driest phases (most likely representing primary igneous compositions) and appropriate partition coefficients, we estimate the H₂O content of the Tissint parent magma to be ≤0.2 wt%.     

Shocked meteorites: Argon-40-argon-39 evidence for multiple impacts

Abstract— To contribute to the understanding of the impact history of asteroids, we performed a high-resolution ⁴⁰Ar-³⁹Ar study of ten moderately to highly shocked chondrites, which we selected according to the shock classification given by Stöffler et al. (1991). Two recent shocked chondrite falls and two highly shocked eucrites completed our sample suite. When possible, we separated impact melt from host rock for separate analysis. In total, we studied 28 samples from 14 meteorites. In some cases, atmospheric Ar that we associate with terrestrial weathering was identified and corrected for. The ages we obtained range between ～100 Ma and ～4.1 Ga and are clearly distinct from primordial ages that correspond to solar system formation. We reproduced the previously reported cluster of L-chondrite ages, ～500 Ma. The most prominent result of our study is that, in the case of chondrites, melts generally are older than host rocks or melt-embedded unmolten rocks. To solve this apparent paradox, we propose that the melt-forming event, which was the most severe shock episode in the history of these meteorites, has not been the only occasion affecting their K-Ar systems. At least one later impact metamorphism must have occured. The response of the K-Ar clock to this second event was more severe in the host rock than in the previously (in the first event) generated melt veins and pockets because of different Ar retention rates. Hence, impact metamorphism on meteorite parent bodies indeed was a multistage process extending in time over billions of years.     

Localized shock melting in lherzolitic shergottite Northwest Africa 1950: Comparison with Allan Hills 77005

Abstract— The lherzolitic Martian meteorite Northwest Africa (NWA) 1950 consists of two distinct zones: 1) low‐Ca pyroxene poikilically enclosing cumulate olivine (Fo_70–75) and chromite, and 2) areas interstitial to the oikocrysts comprised of maskelynite, low‐ and high‐Ca pyroxene, cumulate olivine (Fo_68–71) and chromite. Shock metamorphic effects, most likely associated with ejection from the Martian subsurface by large‐scale impact, include mechanical deformation of host rock olivine and pyroxene, transformation of plagioclase to maskelynite, and localized melting (pockets and veins). These shock effects indicate that NWA 1950 experienced an equilibration shock pressure of 35–45 GPa. Large (millimeter‐size) melt pockets have crystallized magnesian olivine (Fo_78–87) and chromite, embedded in an Fe‐rich, Al‐poor basaltic to picro‐basaltic glass. Within the melt pockets strong thermal gradients (minimum 1 °C/μm) existed at the onset of crystallization, giving rise to a heterogeneous distribution of nucleation sites, resulting in gradational textures of olivine and chromite. Dendritic and skeletal olivine, crystallized in the melt pocket center, has a nucleation density (1.0 × 10³ crystals/mm²) that is two orders of magnitude lower than olivine euhedra near the melt margin (1.6 × 10⁵ crystals/mm²). Based on petrography and minor element abundances, melt pocket formation occurred by in situ melting of host rock constituents by shock, as opposed to melt injected into the lherzolitic target. Despite a common origin, NWA 1950 is shocked to a lesser extent compared to Allan Hills (ALH) 77005 (45–55 GPa). Assuming ejection in a single shock event by spallation, this places NWA 1950 near to ALH 77005, but at a shallower depth within the Martian subsurface. Extensive shock melt networks, the interconnectivity between melt pockets, and the ubiquitous presence of highly vesiculated plagioclase glass in ALH 77005 suggests that this meteorite may be transitional between discreet shock melting and bulk rock melting.     

Primitive olivine‐phyric shergottite NWA 5789: Petrography,mineral chemistry,and cooling history imply a magma similar to Yamato‐980459

Knowledge of Martian igneous basaltic compositions is crucial for constraining mantle evolution, including early differentiation and mantle convection. Primitive magmas provide direct information about their mantle source regions, but most Martian meteorites either contain cumulate olivine or crystallized from fractionated melts. The recently discovered Martian meteorite Northwest Africa (NWA) 5789 is an olivine‐phyric shergottite. NWA 5789 has special significance among the Martian meteorites because it appears to represent one of the most magnesian Martian magmas known, other than Yamato (Y) 980459. Its most magnesian olivine cores (Fo₈₅) are in Mg‐Fe equilibrium with a magma of the bulk rock composition, suggesting that the bulk represents a magma composition. Based on the Al/Ti ratio of its pyroxenes, we infer that the rock began to crystallize at a high pressure consistent with conditions in Mars’ lower crust/upper mantle. It continued and completed its crystallization closer to the surface, where cooling was rapid and produced a mesostasis of radiating sprays of plagioclase and pyroxene. The mineralogy, petrology, mineral chemistry, and bulk rock composition of NWA 5789 are very similar to those of Y‐980459. The similarities between the two meteorites suggest that NWA 5789 (like Y‐980459) represents a primitive, mantle‐derived magma composition. They also suggest the possibility that NWA 5789 and Y‐980459 formed in the same lava flow. However, based on the mineralogy and texture of its mesostasis, NWA 5789 must have cooled more slowly than Y‐980459. NWA 5789 will help elucidate the igneous geology and geochemistry of Mars.     

Terrestrial and Martian weathering signatures of xenon components in shergottite mineral separates

Abstract– Xenon‐isotopic ratios, step‐heating release patterns, and gas concentrations of mineral separates from Martian shergottites Roberts Massif (RBT) 04262, Dar al Gani (DaG) 489, Shergotty, and Elephant Moraine (EET) 79001 lithology B are reported. Concentrations of Martian atmospheric xenon are similar in mineral separates from all meteorites, but more weathered samples contain more terrestrial atmospheric xenon. The distributions of xenon from the Martian and terrestrial atmospheres among minerals in any one sample are similar, suggesting similarities in the processes by which they were acquired. However, in opaque and maskelynite fractions, Martian atmospheric xenon is released at higher temperatures than terrestrial atmospheric xenon. It is suggested that both Martian and terrestrial atmospheric xenon were initially introduced by weathering (low temperature alteration processes). However, the Martian component was redistributed by shock, accounting for its current residence in more retentive sites. The presence or absence of detectable ¹²⁹Xe from the Martian atmosphere in mafic minerals may correspond to the extent of crustal contamination of the rock’s parent melt. Variable contents of excess ¹²⁹Xe contrast with previously reported consistent concentrations of excess ⁴⁰Ar, suggesting distinct sources contributed these gases to the parent magma.     

Expanding the application of the Eu‐oxybarometer to the lherzolitic shergottites and nakhlites: Implications for the oxidation state heterogeneity of the Martian interior

Abstract— Experimentally rehomogenized melt inclusions from the nakhlite Miller Range 03346 (MIL 03346) and the lherzolitic shergottite Allan Hills 77005 (ALH 77005) have been analyzed for their rare earth element (REE) concentrations in order to characterize the early melt compositions of these Martian meteorites and to calculate the oxygen fugacity conditions they crystallized under. D(Eu/Sm)_{pyroxene/melt} values were measured at 0.77 and 1.05 for ALH 77005 and MIL 03346, respectively. These melts and their associated whole rock compositions have similar REE patterns, suggesting that whole rock REE values are representative of those of the early melts and can be used as input into the pyroxene Eu‐oxybarometer for the nakhlites and lherzolitic shergottites. Crystallization fO₂ values of IW + 1.1 (ALH 77005) and IW + 3.2 (MIL 03346) were calculated. Whole rock data from other nakhlites and lherzolitic shergottites was input into the Eu‐oxybarometer to determine their crystallization fO₂ values. The lherzolitic shergottites and nakhlites have fO₂ values that range from IW + 0.4 to 1.6 and from IW + 1.1 to 3.2, respectively. These values are consistent with some previously determined fO₂ estimates and expand the known range of fO₂ values of the Martian interior to four orders of magnitude. The origins of this range are not well constrained. Possible mechanisms for producing this spread in fO₂ values include mineral/melt fractionation, assimilation, shock effects, and magma ocean crystallization processes. Mineral/melt partitioning can result in changes in fO₂ from the start to the finish of crystallization of 2 orders of magnitude. In addition, crystallization of a Martian magma ocean with reasonable initial water content results in oxidized, water‐rich, late‐stage cumulates. Sampling of these oxidized cumulates or interactions between reduced melts and the oxidized material can potentially account for the range of fO₂ values observed in the Martian meteorites.     

Ejection of Martian meteorites

Abstract— We investigated the transfer of meteorites from Mars to Earth with a combined mineralogical and numerical approach. We used quantitative shock pressure barometry and thermodynamic calculations of post‐shock temperatures to constrain the pressure/temperature conditions for the ejection of Martian meteorites. The results show that shock pressures allowing the ejection of Martian meteorites range from 5 to 55 GPa, with corresponding post‐shock temperature elevations of 10 to about 1000 °C. With respect to shock pressures and post‐shock temperatures, an ejection of potentially viable organisms in Martian surface rocks seems possible. A calculation of the cooling time in space for the most highly shocked Martian meteorite Allan Hills (ALH) 77005 was performed and yielded a best‐fit for a post‐shock temperature of 1000 °C and a meteoroid size of 0.4 to 0.6 m. The final burial depths of the sub‐volcanic to volcanic Martian rocks as indicated by textures and mineral compositions of meteorites are in good agreement with the postulated size of the potential source region for Martian meteorites during the impact of a small projectile (200 m), as defined by numerical modeling (Artemieva and Ivanov 2004). A comparison of shock pressures and ejection and terrestrial ages indicates that, on average, highly shocked fragments reach Earth‐crossing orbits faster than weakly shocked fragments. If climatic changes on Mars have a significant influence on the atmospheric pressure, they could account for the increase of recorded ejection events of Martian meteorites in the last 5 Ma.     

Mineralogy,microtexture, and composition of shock‐induced melt pockets in thi Los Angeles basaltic shergottite

Abstract— Analytical electron microscopy of shock features in the basaltic shergottite Los Angeles (stone 1) reveals: 1) shock recorded in the bulk sample; and 2) localized pressure and temperature excursions that have generated melt pockets up to 4 mm in diameter. Bulk shock effects include microfaulting (offsets 1–200 μm), mosaicism, deformed exsolution lamellae and planar fracturing in pyroxene, undulose extinction in whitlockite, mechanical twinning in titanomagnetite and ilmenite, and the transformation of plagioclase to maskelynite (≤4% remnant reduced birefringence). The pressure estimates for bulk shock are 35–40 GPa. Localized shock excursions have generated three types of discrete melt zones (0.07 times 1.3 mm to 3.0 times 3.5 mm apparent diameter) possessing glassy to microcrystalline groundmasses. These melt pockets are differentiated on the basis of size, clast volume, and degree of crystallization and vesiculation. Melt veins and melt dikelets emanate from the melt pockets up to 3 mm into the host rock but do not necessarily connect with other melt pockets. The melt pockets were generated by pressure‐temperature excursions of 60–80 GPa and 1600–2000°C, resulting in discrete melting of adjacent host rock minerals at grain boundary margins. Concentric zoning in the margins of clinopyroxenes coincides with a progressive reduction in birefringence as melt pockets are approached. This suggests that the shock excursions were focused as point sources in the wake of the shock front that induced bulk damage.     

Constraints on the role of impact heating and melting in asteroids

Abstract— Imaging of asteroids Gaspra and Ida and laboratory studies of asteroidal meteorites show that impacts undoubtedly played an important role in the histories of asteroids and resulted in shock metamorphism and the formation of breccias and melt rocks. However, in recent years, impact has also been called upon by numerous authors as the heat source for some of the major geological processes that took place on asteroids, such as global thermal metamorphism of chondrite parent bodies and a variety of melting and igneous events. The latter were proposed to explain the origin of ureilites, aubrites, mesosiderites, the Eagle Station pallasites, acapulcoites, lodranites, and the IAB, IIICD, and HE irons. We considered fundamental observations from terrestrial impact craters, combined with results from laboratory shock experiments and theoretical considerations, to evaluate the efficiency of impact heating and melting of asteroids. Studies of terrestrial impact craters and relevant shock experiments suggest that impact heating of asteroids will produce two types of impact melts: (1) large-scale whole rock melts (total melts, not partial melts) at high shock pressure and (2) localized melts formed at the scale of the mineral constituents (mineral specific or grain boundary melting) at intermediate shock pressures. The localized melts form minuscule amounts of melt that quench and solidify in situ, thus preventing them from pooling into larger melt bodies. Partial melting as defined in petrology has not been observed in natural and experimental shock metamorphism and is thermodynamically impossible in a shock wave-induced transient compression of rocks. The total impact melts produced represent a minuscule portion of the displaced rock volume of the parent crater. Internal differentiation by fractional crystallization is absent in impact melt sheets of craters of sizes that can be tolerated by asteroids, and impact melt rocks are usually clast-laden. Thermal metamorphism of country rocks by impact is extremely minor. Experimental and theoretical considerations suggest that (1) single disruptive impacts cannot raise the average global temperature of strength- or gravity-dominated asteroids by more than a few degrees; (2) cumulative global heating of asteroids by multiple impacts is ineffective for asteroids less than a few hundred kilometers in diameter; (3) small crater size, low gravity, and low impact velocity suggest that impact melt volume in single asteroidal impacts is a very small (0.01–0.1%) fraction of the total displaced crater volume; (4) total impact melt volume formed during the typical lifetime of an asteroid is a small fraction (<0.001) of the volume of impact-generated debris; and (5) much of the impact melt generated on asteroidal targets is ejected from craters with velocities greater than escape velocity and, thus, not retained on the asteroid. The inescapable conclusion from these observations and calculations is that impacts cannot have been the heat source for the origin of the meteorite types listed above, and we must turn to processes other than impact, such as decay of short-lived radionuclides or electromagnetic induction during an early T-tauri phase of the Sun to explain heating and melting of the parent bodies of these meteorites.     

Constraints on the water,chlorine, and fluorine content of the Martian mantle

Previous estimates of the volatile contents of Martian basalts, and hence their source regions, ranged from nearly volatile‐free through estimates similar to those found in terrestrial subduction zones. Here, we use the bulk chemistry of Martian meteorites, along with Martian apatite and amphibole chemistry, to constrain the volatile contents of the Martian interior. Our estimates show that the volatile content of the source region for the Martian meteorites is similar to the terrestrial Mid‐Ocean‐Ridge Mantle source. Chlorine is enriched compared with the depleted terrestrial mantle but is similar to the terrestrial enriched source region; fluorine is similar to the terrestrial primitive mantle; and water is consistent with the terrestrial mantle. Our results show that Martian magmas were not volatile saturated; had water/chlorine and water/fluorine ratios ~0.4–18; and are most similar, in terms of volatiles, to terrestrial MORBs. Presumably, there are variations in volatile content in the Martian interior as suggested by apatite compositions, but more bulk chemical data, especially for fluorine and water, are required to investigate these variations. Finally, the Noachian Martian interior, as exemplified by surface basalts and NWA 7034, may have had higher volatile contents.     

Petrogenesis of basaltic shergottite Northwest Africa 8657: Implications for fO2 correlations and element redistribution during shock melting in shergottites

Northwest Africa (NWA) 8657 is an incompatible trace element-enriched, low-Al basaltic shergottite, similar in texture and chemistry to Shergotty, Zagami, and NWA 5298. It is composed of zoned pyroxene, maskelynite, merrillite, and Ti-oxide minerals with minor apatite, silica, and pyrrhotite. Pyroxene grains are characterized by patchy zoning, with pigeonite or augite cores zoned to Fe-rich pigeonite mantles. The cores have rounded morphologies and irregular margins. Combined with the low Ti/Al of the cores, the morphology and chemistry of the pyroxene grains are consistent with initial crystallization at depth (30–70 km) followed by partial resorption en route to the surface. Enriched rare earth element (REE) equilibrium melt compositions and calculated oxygen fugacities (fO₂) conditions for pigeonite cores indicate that the original parent melts were enriched shergottite magmas that staged in chambers at depth within the Martian crust. NWA 8657 does not represent a liquid but rather entrained a proportion of pyroxene crystals from magma chambers where fractional crystallization was occurring at depth. Variation between fO₂ and bulk-rock (La/Yb)_N of the enriched and intermediate shergottites suggests that oxidation conditions and degree of incompatible element enrichment in the source may not be correlated, as thought previously. Shock melt pockets are characterized by an absence of phosphates and oxide minerals. It is likely that these phases were melted during shock. REEs were redistributed during this process into maskelynite and to a lesser extent the shock melt; however, the overall normalized REE profile of the shock melt is like that of the bulk-rock, but at lower absolute concentrations. Overall, shock melting has had a significant effect on the mineralogy of NWA 8657, especially the distribution of phosphates, which may be significant for geochronological applications of this meteorite and other Martian meteorites with extensive shock melt.     

Characterization of mesostasis regions in lunar basalts: Understanding late‐stage melt evolution and its influence on apatite formation

Recent studies geared toward understanding the volatile abundances of the lunar interior have focused on the volatile‐bearing accessory mineral apatite. Translating measurements of volatile abundances in lunar apatite into the volatile inventory of the silicate melts from which they crystallized, and ultimately of the mantle source regions of lunar magmas, however, has proved more difficult than initially thought. In this contribution, we report a detailed characterization of mesostasis regions in four Apollo mare basalts (10044, 12064, 15058, and 70035) in order to ascertain the compositions of the melts from which apatite crystallized. The texture, modal mineralogy, and reconstructed bulk composition of these mesostasis regions vary greatly within and between samples. There is no clear relationship between bulk‐rock basaltic composition and that of bulk‐mesostasis regions, indicating that bulk‐rock composition may have little influence on mesostasis compositions. The development of individual melt pockets, combined with the occurrence of silicate liquid immiscibility, exerts greater control on the composition and texture of mesostasis regions. In general, the reconstructed late‐stage lunar melts have roughly andesitic to dacitic compositions with low alkali contents, displaying much higher SiO₂ abundances than the bulk compositions of their host magmatic rocks. Relevant partition coefficients for apatite‐melt volatile partitioning under lunar conditions should, therefore, be derived from experiments conducted using intermediate compositions instead of compositions representing mare basalts.     

A new Martian meteorite from Oman: Mineralogy,petrology, and shock metamorphism of olivine‐phyric basaltic shergottite Sayh al Uhaymir 150

Abstract— The Sayh al Uhaymir (SaU) 150 meteorite was found on a gravel plateau, 43.3 km south of Ghaba, Oman, on October 8, 2002. Oxygen isotope (δ¹⁷O 2.78; δ¹⁸O 4.74), CRE age (?1.3 Ma), and noble gas studies confirm its Martian origin. SaU 150 is classified as an olivine‐phyric basalt, having a porphyritic texture with olivine macrocrysts set in a finer‐grained matrix of pigeonite and interstitial maskelynite, with minor augite, spinel, ilmenite, merrillite, pyrrhotite, pentlandite, and secondary (terrestrial) calcite and iron oxides. The bulk rock composition, in particular mg (68) [molar Mg/(Mg + Fe) x 100], Fe/Mn (37.9), and Na/Al (0.22), are characteristic of Martian meteorites. Based on mineral compositions, cooling rates determined from crystal morphology, and crystal size distribution, it is deduced that the parent magma formed in a steady‐state growth regime (magma chamber) that cooled at <°C/hr. Subsequent eruption as a thick lava flow or hypabyssal intrusion entrained a small fraction of xenocrystic olivine and gave rise to a magmatic foliation, with slow cooling allowing for near homogenization of igneous minerals. SaU 150 experienced an equilibration shock pressure of 33–45 GPa in a single impact event. Post‐shock heat gave rise to localized melting (?11 vol%). Larger volume melts remained fluid after pressure release and crystallized dendritic olivine and pyroxene with fractal dimensions of 1.80–1.89 and 1.89–1.95, respectively, at ‐ΔT >70–365 °C. SaU 150 is essentially identical to SaU 005/094, all representing samples of the same fall that are similar to, but distinct from, the DaG shergottites.     

Glass‐bearing inclusions in Shergotty and Chassigny: Consistent samples of a primary trapped melt?

Glass‐bearing inclusions hosted by different mineral phases in SNC meteorites provide important information on the conditions that prevailed during formation of early phases and/or on the composition of the primary trapped liquids/melts of these rocks. Although extensive previous work has been reported on such inclusions, several questions are still unresolved. We performed a chemical and petrographic study of the constituents (glasses and mineral assemblage) of glassy and multiphase inclusions in Shergotty and Chassigny. We focused on obtaining accurate trace element contents of glasses and co‐existing minerals and discussing their highly variable REE contents. Our results reveal an unusual geochemistry of trace element contents that appear to be independent of their major element compositions. Chemical equilibrium between phases inside inclusions as well as between glasses and host minerals could not be established. The LREE contents of glasses in glass inclusions can vary by up to two orders of magnitude. The depletion in trace element abundances shown by glasses seem to be inconsistent with these phases being residual melts. The light lithophile element contents of glasses are highly variable with enrichment in incompatible elements (e.g., Be, Sr, Ba, and LREE) indicating some processes involving percolation of fluids. All of these features are incompatible with glass‐bearing inclusions in the host minerals acting as closed systems preserving unmodified primary liquids/melts. Glass‐bearing inclusions in Shergotty and Chassigny appear to have been altered (as was the rock itself) by different postformational processes (e.g., shock, metamorphism, metasomatic [?] fluids) that affected these meteorites with different degree of intensity. Our results indicate that these inclusions could not preserve a reliable sample of the primary trapped melt.     

Shock and thermal history of Northwest Africa 4859, an annealed impact‐melt breccia of LL chondrite parentage containing unusual igneous features and pentlandite

Abstract– Northwest Africa 4859 (NWA 4859) is a meteorite of LL chondrite parentage that shows unusual igneous features and contains widely distributed pentlandite. The most obvious unusual feature is a high proportion of large (≤3 cm diameter) igneous‐textured enclaves (LITEs), interpreted as shock melts that were intruded into an LL chondrite host. One such LITE appears to have been produced by whole rock melting of LL chondrite, initial rapid partial crystallization, and subsequent slow cooling of the residual melt in the host to produce a differentiated object. Other unusual features include mm‐sized “overgrowth objects,” fine‐grained plagioclase‐rich bands, and coarse troilite (≤7 mm across) grains. All these features are interpreted as having crystallized from melts produced by a single transient shock event, followed by slow cooling. A subsequent shock event of moderate (S3) intensity produced veining and transformed some of the pyroxene into the clinoenstatite polytype. Pentlandite (together with associated troilite) in NWA 4859 probably formed by the breakdown of a monosulfide precursor phase at low temperature (≤230 °C) following the second shock event. NWA 4859 is interpreted to be an unusual impact‐melt breccia that contains shock melt which crystallized in different forms at depth within the parent body.     

Ni/S/Cl systematics and the origin of impact‐melt glasses in Martian meteorite Elephant Moraine 79001

Martian meteorite Elephant Moraine A79001 (EET 79001) has received considerable attention for the unusual composition of its shock melt glass, particularly its enrichment in sulfur relative to the host shergottite. It has been hypothesized that Martian regolith was incorporated into the melt or, conversely, that the S‐enrichment stems from preferential melting of sulfide minerals in the host rock during shock. We present results from an electron microprobe study of EET 79001 including robust measurements of major and trace elements in the shock melt glass (S, Cl, Ni, Co, V, and Sc) and minerals in the host rock (Ni, Co, and V). We find that both S and major element abundances can be reconciled with previous hypotheses of regolith incorporation and/or excess sulfide melt. However, trace element characteristics of the shock melt glass, particularly Ni and Cl abundances relative to S, cannot be explained either by the incorporation of regolith or sulfide minerals. We therefore propose an alternative hypothesis whereby, prior to shock melting, portions of EET 79001 experienced acid‐sulfate leaching of the mesostasis, possibly groundmass feldspar, and olivine, producing Al‐sulfates that were later incorporated into the shock melt, which then quenched to glass. Such activity in the Martian near‐surface is supported by observations from the Mars Exploration Rovers and laboratory experiments. Our preimpact alteration model, accompanied by the preferential survival of olivine and excess melting of feldspar during impact, explains the measured trace element abundances better than either the regolith incorporation or excess sulfide melting hypothesis does.     

Shock‐induced melting,recrystallization, and exsolution in plagioclase from the Martian lherzolitic shergottite GRV 99027

Abstract— Plagioclase in the Martian lherzolitic shergottite Grove Mountains (GRV) 99027 was shocked, melted, and recrystallized. The recrystallized plagioclase contains lamellae of pyroxene, olivine, and minor ilmenite (<1 μm wide). Both the pyroxene and the olivine inclusions enclosed in plagioclase and grains neighboring the plagioclase were partially melted into plagioclase melt pools. The formation of these lamellar inclusions in plagioclase is attributed to exsolution from recrystallizing melt. Distinct from other Martian meteorites, GRV 99027 contains no maskelynite but does contain recrystallized plagioclase. This shows that the meteorite experienced a slower cooling than maskelynite‐bearing meteorites. We suggest that the parent rock of GRV 99027 could have been embedded in hot rocks, which facilitated a more protracted cooling history.     

Petrography,mineral chemistry,and crystallization history of olivine‐phyric shergottite NWA 6234: A new melt composition

Knowledge of Martian igneous and mantle compositions is crucial for understanding Mars' mantle evolution, including early differentiation, mantle convection, and the chemical alteration at the surface. Primitive magmas provide the most direct information about their mantle source regions, but most Martian meteorites either contain cumulate olivine or crystallized from fractionated melts. The new Martian meteorite Northwest Africa (NWA) 6234 is an olivine‐phyric shergottite. Its most magnesian olivine cores (Fo₇₈) are in Mg‐Fe equilibrium with a magma of the bulk rock composition, suggesting that it represents a melt composition. Thermochemical calculations show that NWA 6234 not only represents a melt composition but is a primitive melt derived from an approximately Fo₈₀ mantle. Thus, NWA 6234 is similar to NWA 5789 and Y 980459 in the sense that all three are olivine‐phyric shergottites and represent primitive magma compositions. However, NWA 6234 is of special significance because it represents the first olivine‐phyric shergottite from a primitive ferroan magma. On the basis of Al/Ti ratio of pyroxenes in NWA 6234, the minor components in olivine and merrillite, and phosphorus zoning of olivine, we infer that the rock crystallized completely at pressures consistent with conditions in Mars' upper crust. The textural intergrowths of the two phosphates (merrillite and apatite) indicate that at a very last stage of crystallization, merrillite reacted with an OH‐Cl‐F‐rich melt to form apatite. As this meteorite crystallized completely at depth and never erupted, it is likely that its apatite compositions represent snapshots of the volatile ratios of the source region without being affected by degassing processes, which contain high OH‐F content.     

Physical properties of Martian meteorites: Porosity and density measurements

Abstract— Martian meteorites are fragments of the Martian crust. These samples represent igneous rocks, much like basalt. As such, many laboratory techniques designed for the study of Earth materials have been applied to these meteorites. Despite numerous studies of Martian meteorites, little data exists on their basic structural characteristics, such as porosity or density, information that is important in interpreting their origin, shock modification, and cosmic ray exposure history. Analysis of these meteorites provides both insight into the various lithologies present as well as the impact history of the planet's surface. We present new data relating to the physical characteristics of twelve Martian meteorites. Porosity was determined via a combination of scanning electron microscope (SEM) imagery/image analysis and helium pycnometry, coupled with a modified Archimedean method for bulk density measurements. Our results show a range in porosity and density values and that porosity tends to increase toward the edge of the sample. Preliminary interpretation of the data demonstrates good agreement between porosity measured at 100× and 300× magnification for the shergottite group, while others exhibit more variability. In comparison with the limited existing data for Martian meteorites we find fairly good agreement, although our porosity values typically lie at the low end of published values. Surprisingly, despite the increased data set, there is little by way of correlation between either porosity or density with parameters such as shock effect or terrestrial residency. Further data collection on additional meteorite samples is required before more definitive statements can be made concerning the validity of these observations.