Melt inclusions in augite of the Nakhla martian meteorite: Evidence for basaltic parental melt

Abstract— Nakhla contains crystallized melt inclusions that were trapped in augite and olivine when these phases originally formed on Mars. Our study involved rehomogenization (slow‐heating and fast‐heating) experiments on multiphase melt inclusions in Nakhla augite. We studied melt inclusions trapped in augite because this phase re‐equilibrated with the external melt to a lesser extent than olivine and results could be directly compared with previous Nakhla melt inclusion studies. Following heating and homogenization of encapsulated melt inclusions, single mineral grains were mounted and polished to expose inclusions. Major element chemistry was determined by electron microprobe. The most primitive melt inclusion analyzed in Nakhla NA03 is basaltic and closely matches previously reported nakhlite parent melt compositions. MELTS equilibrium and fractional crystallization models calculated for NA03 and previous Nakhla parent melt estimates at QFM and QFM‐1 produced phase assemblages and compositions that can be compared to Nakhla. Of these models, equilibrium crystallization of NA03 at QFM‐1 produced the best match to mineral phases and compositions in Nakhla. In all models, olivine and augite co‐crystallize, consistent with the hypothesis that olivine is not xenocrystic but has undergone subsolidus re‐equilibration. In addition, measured melt inclusion compositions plot along the MELTS‐calculated liquid line of descent and may represent pockets of melt trapped at various stages during crystallization. We attempt to resolve discrepancies between previous estimates of the Nakhla parental melt composition and to reinterpret the results of a previous study of rehomogenized melt inclusions in Nakhla. Melt inclusions demonstrate that Nakhla is an igneous rock whose parent melt composition and crystallization history reflect planetary igneous processes.     

Melt inclusions in augite from the nakhlite meteorites: A reassessment of nakhlite parental melt and implications for petrogenesis

Abstract– The nakhlites, a subgroup of eight clinopyroxenites thought to come from a single geological unit at the Martian surface, show melt inclusions in augite and olivine. In contrast to olivine‐hosted melt inclusions, augite‐hosted melt inclusions are not surrounded by fractures, and are thus considered preferential candidates for reconstructing parent liquid compositions. Furthermore, two types of augite‐hosted melt inclusion have been defined and characterized in four different nakhlites (Northwest Africa [NWA] 817, Nakhla, Governador Valadares, and NWA 998): Type‐I isolated inclusions in augite cores that contain euhedral to subhedral augite, Ti‐magnetite, and pigeonite plus silica‐rich glass and a gas bubble; Type‐II microinclusions that form trails crosscutting host augite crystals. Fast‐heating experiments were performed on selected pristine primary augite‐hosted melt inclusions from these four samples. Of these, only data from Nakhla were considered robust for reconstruction of a nakhlite parental magma composition (NPM). Based upon careful petrographic selection and consideration of iron‐magnesium ratios, our data are used to propose an NPM, which is basaltic (49.1 wt% SiO₂), of high Ca/Al (1.95), and K₂O‐poor (0.32 wt%). Thermodynamic modeling at an oxygen fugacity one log unit below the QFM buffer using the MELTS and PETROLOG programs implies that Mg‐rich olivine was not a liquidus phase for this composition. Our analysis is used to suggest that olivine megacrysts found in the nakhlites are unlikely to have coprecipitated with augite, and thus may have been introduced during or subsequent to accumulation in the magma chamber, possibly from more evolved portions of the same chamber.     

K2O‐rich trapped melt in olivine in the Nakhla meteorite: Implications for petrogenesis of nakhlites and evolution of the Martian mantle

We used new analytical and theoretical methods to determine the major and minor element compositions of the primary trapped liquid (PTLs) represented by melt inclusions in olivine and augite in the Martian clinopyroxenite, Nakhla, for comparison with previously proposed compositions for the Nakhla (or nakhlite) parent magma. We particularly focused on obtaining accurate K₂O contents, and on testing whether high K₂O contents and K₂O/Na₂O ratios obtained in previous studies of melt inclusions in olivine in Nakhla could have been due to unrepresentative sampling, systematic errors arising from electron microprobe techniques, late alteration of the inclusions, and/or boundary layer effects. Based on analyses of 35 melt inclusions in olivine cores, the PTL in olivine, PTL_oliv, contained (by wt) approximately 47% SiO₂, 6.3% Al₂O₃, 9.6% CaO, 1.8% K₂O, and 0.9% Na₂O, with K₂O/Na₂O = 2.0. We infer that the high K₂O content of PTL_oliv is not due to boundary layer effects and represents a real property of the melt from which the host olivine crystallized. This melt was cosaturated with olivine and augite. Its mg# is model‐dependent and is constrained only to be ≥19 (equilibrium Fo = 40). Based on analyses of 91 melt inclusions in augite cores, the PTL in augite, PTL_aug, contained (by wt) 53–54% SiO₂, 7–8% Al₂O₃, 0.8–1.1% K₂O, and 1.1–1.4% Na₂O, with K₂O/Na₂O = 0.7–0.8. This K₂O content and K₂O/Na₂O ratio are significantly higher than inferred in studies of melt inclusions in augite in Nakhla by experimental rehomogenization. PTL_aug was saturated only with augite, and in equilibrium with augite cores of mg# 62. PTL_aug represents the Nakhla parent magma, and does not evolve to PTL_oliv by fractional crystallization. We therefore conclude that olivine cores in Nakhla (and, by extension, other nakhlites) are xenocrystic. We propose that PTL_oliv and PTL_aug were generated from the same source region. PTL_oliv was generated first and emplaced to form olivine‐rich cumulate rocks. Shortly thereafter, PTL_aug was generated and ascended through these olivine‐rich cumulates, incorporating fragments of wallrock that became the xenocrystic olivine cores in Nakhla. The Nakhla (nakhlite) mantle source region was pyroxenitic with some olivine, and could have become enriched in K relative to Na via metasomatism. A high degree of melting of this source produced the silica‐poor, alkali‐rich magma PTL_oliv. Further ascension and decompression of the source led to generation of the silica‐rich, relatively alkali‐poor magma PTL_aug. Potassium‐rich magmas like those involved in the formation of the nakhlites represent an important part of the diversity of Martian igneous rocks.     

Alteration assemblages in the nakhlites: Variation with depth on Mars

Secondary mineral assemblages in the nakhlite meteorites, Lafayette, Governador Valadares (GV), Nakhla, Yamato (Y)‐000593/Y‐000749 have been studied using scanning electron microscopy, transmission electron microscopy, and electron probe micro analysis. The different nakhlites have distinctive secondary assemblages in their olivine grains and mesostases, showing compositional fractionation correlated with their relative depths below the Martian surface. Fracture‐filled veins in Lafayette at the bottom of the pile consist of a siderite‐phyllosilicate‐Fe oxide‐hydrated silicate gel assemblage. Corresponding veins in Nakhla and GV further up the pile are predominantly a siderite‐gel assemblage, with additional evaporites including gypsum. Y‐000593/Y‐000749 veins are dominated by gel. The gel’s Mg/(Mg + Fe) ratio decreases from Lafayette (0.37) to GV (0.32), Nakhla (0.24), and Y‐000593 (0.15). We suggest that hydrothermal fluid flowed up this depth profile, initiated by melting of buried H₂O–CO₂ ice. Our results show a complex mix of Fe‐rich phyllosilicate within the veins and mesostasis of Lafayette with d‐spacings of 0.7–1.1 nm suggesting a mixture of smectite and serpentine. The phyllosilicate formed at close to neutral pH, ≤150 °C. We also suggest that water rock ratios (W/R) of 1–10 occurred in Lafayette with smaller values for the other nakhlites. This is reflected in the volume of alteration minerals: 10% of olivine in Lafayette to 3% in Nakhla. Textural evidence of rapid cooling, together with the W/R and likely fluid velocities, suggest that the secondary assemblages formed quickly, e.g., within months. A model is proposed in which the secondary assemblages formed in an impact‐induced hydrothermal system terminated by precipitation of the gel and evaporation of soluble salts.     

Opal‐A in the Nakhla meteorite: A tracer of ephemeral liquid water in the Amazonian crust of Mars

The nakhlite meteorites are clinopyroxenites that are derived from a ~1300 million year old sill or lava flow on Mars. Most members of the group contain veins of iddingsite whose main component is a fine‐grained and hydrous Fe‐ and Mg‐rich silicate. Siderite is present in the majority of veins, where it straddles or cross‐cuts the Fe‐Mg silicate. This carbonate also contains patches of ferric (oxy)hydroxide. Despite 40 years of investigation, the mineralogy and origins of the Fe‐Mg silicate is poorly understood, as is the paragenesis of the iddingsite veins. Nanometer‐scale analysis of Fe‐Mg silicate in the Nakhla meteorite by electron and X‐ray imaging and spectroscopy reveals that its principal constituents are nanoparticles of opal‐A. This hydrous and amorphous phase precipitated from acidic solutions that had become supersaturated with respect to silica by dissolution of olivine. Each opal‐A nanoparticle is enclosed within a ferrihydrite shell that formed by oxidation of iron that had also been liberated from the olivine. Siderite crystallized subsequently and from solutions that were alkaline and reducing, and replaced both the nanoparticles and olivine. The fluids that formed both the opal‐A/ferrihydrite and the siderite were sourced from one or more reservoirs in contact with the Martian atmosphere. The last event recorded by the veins was alteration of the carbonate to a ferric (oxy)hydroxide that probably took place on Mars, although a terrestrial origin remains possible. These results support findings from orbiter‐ and rover‐based spectroscopy that opaline silica was a common product of aqueous alteration of the Martian crust.     

Comparisons of the four Miller Range nakhlites,MIL 03346, 090030, 090032 and 090136: Textural and compositional observations of primary and secondary mineral assemblages

Abstract– Petrological and geochemical analyses of Miller Range (MIL) 03346 indicate that this meteorite originated from the same augitic cumulate layer(s) as the nakhlite Martian meteorites, but underwent rapid cooling prior to complete crystallization. As with the other nakhlites, MIL 03346 contains a secondary alteration assemblage, in this case consisting of iddingsite‐like alteration veins in olivine phenocrysts, Fe‐oxide alteration veins associated with the mesostasis, and Ca‐ and K,Fe‐sulfate veins. We compared the textural and mineralogical compositions of MIL 090030, 090032, and 090136 with MIL 03346, focusing on the composition and Raman spectra of the alteration assemblages. These observations indicate that the meteorites are paired, and that the preterrestrial olivine‐bound alteration assemblages were produced by weakly acidic brine. Although these alteration assemblages resemble similar assemblages in Nakhla, the absence of siderite and halite in the Miller Range nakhlites indicates that the parental alteration brine was comparatively HCO₃^? depleted, and less concentrated, than that which altered Nakhla. This indicates that the Miller Range nakhlite alteration brine experienced a separate evolutionary pathway to that which altered Nakhla, and therefore represents a separate branch of the Lafayette‐Nakhla evaporation sequence. Thin‐sections cut from the internal portions of these meteorites (away from any fusion crust or terrestrially exposed edge), contain little Ca‐sulfate (identified as gypsum), and no jarosite, whereas thin‐sections with terrestrially exposed edges have much higher sulfate abundances. These observations suggest that at least the majority of sulfate within the Miller Range nakhlites is terrestrially derived.     

Evidence for silicate dissolution on Mars from the Nakhla meteorite

Veins containing carbonates, hydrous silicates, and sulfates that occur within and between grains of augite and olivine in the Nakhla meteorite are good evidence for the former presence of liquid water in the Martian crust. Aqueous solutions gained access to grain interiors via narrow fractures, and those fractures within olivine whose walls were oriented close to (001) were preferentially widened by etching along [001]. This orientation selective dissolution may have been due to the presence within olivine of shock‐formed [001](100) and [001]{110} screw dislocations. The duration of etching is likely to have been brief, possibly less than a year, and the solutions responsible were sufficiently cool and reducing that laihunite did not form and Fe liberated from the olivine was not immediately oxidized. The pores within olivine were mineralized in sequence by siderite, nanocrystalline smectite, a Fe‐Mg phyllosilicate, and then gypsum, whereas only the smectite occurs within augite. The nanocrystalline smectite was deposited as submicrometer thick layers on etched vein walls, and solution compositions varied substantially between and sometimes during precipitation of each layer. Together with microcrystalline gypsum the Fe‐Mg phyllosilicate crystallized as water briefly returned to some of the veins following desiccation fracturing of the smectite. These results show that etching of olivine enhanced the porosity and permeability of the nakhlite parent rock and that dissolution and secondary mineralization took place within the same near‐static aqueous system.     

Symplectic exsolution in olivine from the Nakhla martian meteorite

Abstract— The Nakhla meteorite, commonly accepted to have originated from Mars, is a cumulus clinopyroxenite with ～10 vol% of Fe‐rich olivine. Almost all olivine grains in Nakhla contain dark lamellar inclusions (less than 2–3 μm wide). High‐resolution scanning and transmission electron microscopy revealed that the inclusions are complex intergrowths of augite and magnetite. Such a symplectic intergrowth of augite and magnetite in olivine was known in some terrestrial rocks, lunar rocks, and a few meteorites. The inclusion in Nakhla olivine is the first symplectite found in a martian rock. Apparently, the presence of Fe³+ in olivine under an oxidizing condition on Mars caused symplectic exsolution at high temperature (>900 °C) during cooling.     

Defining the mechanisms that disturb the Sm‐Nd isotopic systematics of the Martian meteorites: Examples from Dar al Gani 476 and Allan Hills 77005

Abstract— Microbeam studies of Martian meteorites Dar al Gani (DaG) 476 and Allan Hills (ALH) 77005 have been conducted to identify potential causes of disequilibrium exhibited in their Sm‐Nd isotopic systematics. Olivine and maskelynite mineral fractions on the DaG 476 isochron are displaced relative to their positions as dictated by measured mineral compositions. The olivine mineral fractions from ALH 77005 not only have a relatively low Sm/Nd ratio, but appear to contain an unradiogenic component that shifts the olivine mineral fraction off the isochron defined by the pyroxene and maskelynite mineral fractions. Trace components such as melt inclusions, impact melt, high‐Si mesostasis, and altered olivine were analyzed using scanning electron microscopy, quantitative electron microscopy, and secondary ion mass spectrometry to determine their potential for disturbing the isotopic systematics of the mineral fractions, assuming that the mineral fractions were not completely pure. Mixing models indicate that the presence of melt inclusions in the DaG 476 olivine mineral fraction lowered its Sm/Nd ratio. The maskelynite mineral fraction contains a related but more evolved mesostasis component that raised the Sm/Nd ratio of the fraction. The position of two olivine mineral fractions below the ALH 77005 isochron is interpreted to reflect small additions of impact melt with a light rare earth element enriched pattern and a non‐indigenous, unradiogenic Nd component. Furthermore, the presence of rare earth elements in olivine and maskelynite from both igneous and non‐igneous components such as melt inclusions, mesostasis, and impact melt is observed on a fine (<30 μm) scale. Despite the addition of this material, the Sm‐Nd ages are not affected. This study demonstrates that detailed mineral separation procedures as employed by modern geochronology laboratories permit reliable ages to be derived from shocked and altered samples.     

Caleta el Cobre 022 Martian meteorite: Increasing nakhlite diversity

Caleta el Cobre (CeC) 022 is a Martian meteorite of the nakhlite group, showing an unbrecciated cumulate texture, composed mainly of clinopyroxene and olivine. Augite shows irregular core zoning, euhedral rims, and thin overgrowths enriched in Fe relative to the core. Low‐Ca pyroxene is found adjacent to olivine. Phenocrysts of Fe‐Ti oxides are titanomagnetite with exsolutions of ilmenite/ulvöspinel. Intercumulus material consists of both coarse plagioclase and fine‐grained mesostasis, comprising K‐feldspars, pyroxene, apatite, ilmenite, Fe‐Ti oxides, and silica. CeC 022 shows a high proportion of Martian aqueous alteration products (iddingsite) in olivine (45.1 vol% of olivine) and mesostasis. This meteorite is the youngest nakhlite with a distinct Sm/Nd crystallization age of 1.215 ± 0.067 Ga. Its ejection age of 11.8 ± 1.8 Ma is similar to other nakhlites. CeC 022 reveals contrasted cooling rates with similarities with faster cooled nakhlites, such as Northwest Africa (NWA) 817, NWA 5790, or Miller Range 03346 nakhlites: augite irregular cores, Fe‐rich overgrowths, fine‐grained K‐feldspars, quenched oxides, and high rare earth element content. CeC 022 also shares similarities with slower cooled nakhlites, including Nakhla and NWA 10153: pyroxene modal abundance, pyroxenes crystal size distribution, average pyroxene size, phenocryst mineral compositions, unzoned olivine, and abundant coarse plagioclase. Moreover, CeC 022 is the most magnetic nakhlite and represents an analog source lithology for the strong magnetization of the Martian crust. With its particular features, CeC 022 must originate from a previously unsampled sill or flow in the same volcanic system as the other nakhlites, increasing Martian sample diversity and our knowledge of nakhlites.     

Chemical layering in the upper mantle of Mars: Evidence from olivine‐hosted melt inclusions in Tissint

Melting of Martian mantle, formation, and evolution of primary magma from the depleted mantle were previously modeled from experimental petrology and geochemical studies of Martian meteorites. Based on in situ major and trace element study of a range of olivine‐hosted melt inclusions in various stages of crystallization of Tissint, a depleted olivine–phyric shergottite, we further constrain different stages of depletion and enrichment in the depleted mantle source of the shergottite suite. Two types of melt inclusions were petrographically recognized. Type I melt inclusions occur in the megacrystic olivine core (Fo_76‐70), while type II melt inclusions are hosted by the outer mantle of the olivine (Fo_66‐55). REE‐plot indicates type I melt inclusions, which are unique because they represent the most depleted trace element data from the parent magmas of all the depleted shergottites, are an order of magnitude depleted compared to the type II melt inclusions. The absolute REE content of type II displays parallel trend but somewhat lower value than the Tissint whole‐rock. Model calculations indicate two‐stage mantle melting events followed by enrichment through mixing with a hypothetical residual melt from solidifying magma ocean. This resulted in ~10 times enrichment of incompatible trace elements from parent magma stage to the remaining melt after 45% crystallization, simulating the whole‐rock of Tissint. We rule out any assimilation due to crustal recycling into the upper mantle, as proposed by a recent study. Rather, we propose the presence of Al, Ca, Na, P, and REE‐rich layer at the shallower upper mantle above the depleted mantle source region during the geologic evolution of Mars.     

Sulfide petrology of four nakhlites: Northwest Africa 817, Northwest Africa 998, Nakhla,and Governador Valadares

Abstract– The nakhlites contain small proportions of Cu‐Fe‐Ni sulfide minerals; we have studied these sulfides in Northwest Africa (NWA) 998, Nakhla, Governador Valadares, and NWA 817 with optical microscopy, scanning electron microscope, and electron microprobe. Modal abundances of magmatic sulfides, as estimated by image analysis on thin section, are uniformly low (0.02 to 0.05 ± 0.03 vol%), i.e., a factor 5 lower than in shergottites. Sulfides occur within the glassy mesostasis, as composite two‐phase Fe‐Ti oxide‐sulfide grains, intimately associated with interstitial grains or locally enclosed in postcumulus melt inclusions (e.g., Governador Valadares) in olivine. They exhibit a uniform low‐Ni monoclinic pyrrhotite composition ± chalcopyrite. There is a gradation of sulfide grain sizes and textures across the nakhlites flow(s): droplets in NWA 817; resorbed blebs in Governador Valadares; more massive, true intercumulus blebs in Nakhla and NWA 998. These nakhlites also show evidence for sulfide weathering. Hot desert finds (e.g., NWA 998 and NWA 817) show a few percent fracture‐filling iron (oxy) hydroxides of likely terrestrial origin. Original sulfides are 50% altered in our NWA 998 section, with iron (oxy) hydroxides at grain boundaries and as complete pseudomorphs. The compositions of unaltered pyrrhotites are homogeneous, close to that of the monoclinic endmember Fe₇S₈, and are too sulfur‐rich to have been in chemical equilibrium with the late magmatic redox state fixed by the fayalite‐magnetite‐quartz buffer. Therefore, the compositions of the pyrrhotites must have been altered during the later stages of magmatic crystallization, by assimilation of S‐rich regolith and hydrothermal circulation.     

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.     

Experimental petrology of the basaltic shergottite Yamato‐980459: Implications for the thermal structure of the Martian mantle

Abstract— The Martian meteorite Yamato (Y‐) 980459 is an olivine‐phyric shergottite. It has a very primitive character and may be a primary melt of the Martian mantle. We have conducted crystallization experiments on a synthetic Y‐980459 composition at Martian upper mantle conditions in order to test the primary mantle melt hypothesis. Results of these experiments indicate that the cores of the olivine megacrysts in Y‐980459 are in equilibrium with a melt of bulk rock composition, suggesting that these megacrysts are in fact phenocrysts that grew from a magma of the bulk rock composition. Multiple saturation of the melt with olivine and a low‐calcium pyroxene occurs at approximately 12 ± 0.5 kbar and 1540 ± 10°C, suggesting that the meteorite represents a primary melt that separated from its mantle source at a depth of ?100 km. Several lines of evidence suggest that the Y‐980459 source underwent extensive melting prior to and/or during the magmatic event that produced the Y‐980459 parent magma. When factored into convective models of the Martian interior, the high temperature indicated for the upper Martian mantle and possibly high melt fraction for the Y‐980459 magmatic event suggests a significantly higher temperature at the core‐mantle boundary than previously estimated.     

An American on Paris: Extent of aqueous alteration of a CM chondrite and the petrography of its refractory and amoeboid olivine inclusions

Paris is the least aqueously altered CM chondrite identified to date, classified as subtype 2.7; however, literature data indicate that some regions of this apparently brecciated meteorite may be subtype 2.9. The suite of CAIs in Paris includes 19% spinel–pyroxene inclusions, 19% spinel inclusions, 8% spinel–pyroxene–olivine inclusions, 43% pyroxene inclusions, 8% pyroxene–olivine inclusions, and 3% hibonite‐bearing inclusions. Both simple and complex inclusions are present; some have nodular, banded, or distended structures. No melilite was identified in any of the inclusions in the present suite, but other recent studies have found a few rare occurrences of melilite in Paris CAIs. Because melilite is highly susceptible to aqueous alteration, it is likely that it was mostly destroyed during early‐stage parent‐body alteration. Two of the CAIs in this study are part of compound CAI–chondrule objects. Their presence suggests that there were transient heating events (probably associated with chondrule formation) in the nebula after chondrules and CAIs were admixed. Also present in Paris are a few amoeboid olivine inclusions (AOI) consisting of relatively coarse forsterite rims surrounding fine‐grained, porous zones containing diopside and anorthite. The interior regions of the AOIs may represent fine‐grained rimless CAIs that were incorporated into highly porous forsterite‐rich dustballs. These assemblages were heated by an energy pulse that collapsed and coarsened their rims, but failed to melt their interiors.     

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.     

Cover

Phase map of an iddingsite vein in an olivine grain from the Nakhla meteorite made using multiple linear least squares fitting of electron energy loss spectroscopy data (green ‐ olivine, blue ‐ siderite, pink ‐ ferric oxyhydroxide, orange ‐ Fe‐Mg silicate). The detailed structure of the Fe‐Mg silicate is shown in the inset, which is a spectroscopic map of iron (red), magnesium (green) and silicon (blue) showing the nanoscale structure of opal‐A spheres in a Fe‐Mg‐rich matrix. Martin Lee et al. discuss the details in their article on pp. 1362–1377. Image prepared by Ian MacLaren.     

Alkalic parental magmas for chassignites?

Abstract Detailed analysis of cumulate and melt inclusion assemblages in the chassignites provide important constraints on the nature of the melt trapped as inclusions in cumulus olivine (and, by extension, parental magma compositions), the pressures of crystallization, and magmatic volatile contents. These mineral assemblages show strong similarities to the experimental fractionation assemblages that produce the sodic silica‐saturated alkalic lavas on Earth (e.g., Ascension Island, Azores, the Nandewar volcano of Australia). The experimental assemblages were produced from silica‐saturated hawaiite at pressures above 4.3 kbar with dissolved water contents above 0.5 wt%. Such pressures are consistent with Ti:Al ratios of the melt‐inclusion pyroxenes in the Chassigny meteorite. Pyroxene compositions suggest early high crystallization temperatures and thus relatively low initial water and F contents. Feldspars indicate that melt evolution proceeded to rhyolite compositions both within the interstices of the cumulate olivine and within the melt inclusions, even though rhyolitic glass is only found within olivine‐hosted polyphase melt inclusions. The observed rhyolite glass is compositionally similar to the alkali‐rich rhyolite of Ascension Island which is produced experimentally by crystallization of hawaiite. It is proposed that the melt trapped in cumulus olivine of the Chassigny dunite was similar to a terrestrial silica‐saturated hawaiite, while that trapped in olivine of the Northwest Africa (NWA) 2727 dunite was less evolved, perhaps mildly alkalic basalt. Melts similar to terrestrial intra‐plate tholeiite could be parental to the cumulus minerals and evolve upon crystallization at pressures above 4.3 kbar and water contents above ?0.4 wt% to mildly alkalic basalt, silica‐saturated hawaiite, and alkali‐rich rhyolite. The melt inclusion assemblages are inconsistent with either crystallization of a low‐Al, high‐Fe basalt, or low‐pressure crystallization of a terrestrial‐like tholeiite.     

Deciphering the nebular and asteroidal record of silicates and organic material in the matrix of the reduced CV3 chondrite Vigarano

We have conducted scanning electron microscope (SEM) and transmission electron microscope (TEM) studies of a variety of occurrences of matrix in the reduced CV3 chondrite breccia Vigarano. Matrix, which occurs as clastic interchondrule material and finer‐grained rims, is dominated by morphologically variable olivines that host submicron, hercynitic spinel, and carbonaceous inclusions. Clastic matrix and fine‐grained rims show significant differences in their olivine morphologies, abundance, and composition of olivine inclusions, and characteristics of the carbonaceous matter. We suggest that these differences are the result of different degrees of alteration of clastic matrix and rims and are not due to variability in their precursor materials. Textural and compositional characteristics of olivine in the matrix are consistent with formation by growth, possibly from an amorphous precursor material during asteroidal metamorphism, in the presence of limited quantities of aqueous fluids. Spinel inclusions in olivine may be nebular condensates that acted as seeds for nucleation of olivine or may have formed during metamorphism and were subsequently overgrown by olivine. Carbonaceous material occurs as nanometer‐sized inclusions within olivine in both fine‐grained rims and clastic matrix, but is most abundant as 100–200 nm grains, interstitial to matrix olivines. Most carbonaceous material is amorphous, but poorly graphitized carbon (PGC) also occurs as a minor component in both olivine inclusions and interstitial C. The widespread occurrence of fine‐grained amorphous carbon grains in the interstitial regions between olivine grains may preserve the distribution and grain size of nebular organic material. No clear textural relationships exist between carbonaceous grains and the other mineralogical components of Vigarano matrix that could help constrain the origin of the organic grains (i.e., evidence for Fischer‐Tropsch‐type reactions). Finally, there are considerable differences between matrix olivines in Vigarano in comparison with those in oxidized CV3 chondrites. In particular, the mineralogy and morphology of the matrix olivines and the nature, composition, and distribution of inclusions in the olivine grains are distinct. Based on these differences, we conclude that matrix in the oxidized CV3 chondrites could not have formed by thermal processing of Vigarano‐like material.     

Magmatic history and parental melt composition of olivine‐phyric shergottite LAR 06319: Importance of magmatic degassing and olivine antecrysts in Martian magmatism

Several olivine‐phyric shergottites contain enough olivine that they could conceivably represent the products of closed‐system crystallization of primary melts derived from partial melting of the Martian mantle. Larkman Nunatak (LAR) 06319 has been suggested to represent a close approach to a Martian primary liquid composition based on approximate equilibrium between its olivine and groundmass. To better understand the olivine–melt relationship and the evolution of this meteorite, we report the results of new petrographic and chemical analyses. We find that olivine megacryst cores are generally not in equilibrium with the groundmass, but rather have been homogenized by diffusion to Mg# 72. We have identified two unique grain types: an olivine glomerocryst and an olivine grain preserving a primary magmatic boundary that constrains the time scale of eruption to be on the order of hours. We also report the presence of trace oxide phases and phosphate compositions that suggest that the melt contained approximately 1.1% H₂O and lost volatiles during cooling, also associated with an increase in oxygen fugacity upon degassing. We additionally report in situ rare earth element measurements of the various mineral phases in LAR 06319. Based on these reported trace element abundances, we estimate the oxygen fugacity in the LAR 06319 parent melt early in its crystallization sequence (i.e., at the time of crystallization of the low‐Ca and high‐Ca pyroxenes), the rare earth element composition of the parent melt, and those of melts in equilibrium with later formed phases. We suggest that LAR 06319 represents the product of closed‐system crystallization within a shallow magma chamber, with additional olivine accumulated from a cumulate pile. We infer that the olivine megacrysts are antecrysts, derived from a single magma chamber, but not directly related to the host magma, and suggest that mixing of antecrysts within magma chambers may be a common process in Martian magmatic systems.