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.     

Searching for the source regions of martian meteorites using MGS TES: Integrating martian meteorites into the global distribution of igneous materials on Mars

Abstract— The objective of this study was to identify and map possible source regions for all 5 known martian meteorite lithologies (basalt, lherzolite, clinopyroxenite, orthopyroxenite, and dunite) using data from the Mars Global Surveyor Thermal Emission Spectrometer (MGS TES). We deconvolved the TES data set using laboratory spectra of 6 martian meteorites (Los Angeles, Zagami, ALH A77005, Nakhla, ALH 84001, and Chassigny) as end members, along with atmospheric and surface spectra previously derived from TES data. Global maps (16 pixels/degree) of the distribution of each meteorite end member show that meteorite‐like compositions are not present at or above TES detectability limits over most of the planet's dust‐free regions. However, we have confidently identified local‐scale (100s‐1000s km²) concentrations of olivine‐ and orthopyroxene‐bearing materials similar to ALH A77005, Chassigny, and ALH 84001 in Nili Fossae, in and near Ganges Chasma, in the Argyre and Hellas basin rims, and in Eos Chasma. Nakhla‐like materials are identified near the detection limit throughout the eastern Valles Marineris region and portions of Syrtis Major. Basaltic shergottites were not detected in any spatially coherent areas at the scale of this study. Martian meteorite‐like lithologies represent only a minor portion of the dust‐free surface and, thus, are not representative of the bulk composition of the ancient crust. Meteorite‐like spectral signatures identified above TES detectability limits in more spatially restricted areas (<tens of km) are targets of ongoing analysis.     

40Ar‐39Ar studies of whole rock nakhlites: Evidence for the timing of formation and aqueous alteration on Mars

Abstract— 20–25 mg whole rock samples of the nakhlites Lafayette and Nakhla have been analyzed via the ⁴⁰Ar‐³⁹Ar technique, in part to verify their formation ages, but primarily, in an attempt to determine the timing of aqueous alteration in these martian meteorites. As in previous studies, plateaus in apparent age are observed at about 1300 Ma (1322 ± 10 for Lafayette, 1332 ± 10 and 1323 ± 11 for Nakhla), presumably corresponding to crystallization ages. The plateaus are not entirely flat, perhaps reflecting the effects of recoil during creation of ³⁹Ar in the nuclear irradiation. The first 5–20% of the K‐derived Ar released from all three samples give apparent ages <1300 Ma. Coupled with the fact that chronometric isotopic studies of nakhlites typically show some disturbance, we believe the low temperature pattern represents more recent (than 1300 Ma) formation of martian aqueous alteration products such as iddingsite. No low temperature plateaus are observed. This is consistent with petrographic evidence for multiple formation events, although the lack of low temperature plateaus is far from conclusive. On the other hand, if there was a single time of alteration, we believe that it will be difficult, if not impossible, to determine it using the K‐Ar system.     

Mineralogy of the sources for magnetic anomalies on Mars

Abstract— Recent discovery of intense magnetic anomalies on Mars, which are due to remanent magnetization, requires some explanation for the possible minerals responsible for the anomalous signature. Thermoremanent magnetization (TRM) in single domain (SD) and multidomain (MD) sized magnetite, hematite, and pyrrhotite, all potential minerals, are considered. The intensity of TRM (in 0.05 mT) is in descending order: SD‐sized magnetite, SD‐sized pyrrhotite, MD‐sized hematite, MD‐sized pyrrhotite, MD‐sized magnetite, SD‐sized hematite. The TRM intensity is <4% of the saturation isothermal remanence (SIRM) for all but the MD hematite, which may have >50% of the SIRM. Each of these minerals and estimated concentrations of magnetic remanence carriers (assumed to be titanomagnetite) in the Shergotty‐Nakhla‐Chassigny martian meteorites are used in a thin sheet approximation model to reveal the concentration of each mineral required for the generation of an observed magnetic anomaly (1500 nT at 100 km altitude) assuming TRM acquisition in a 0.05 mT magnetic field.     

Fractionated martian atmosphere in the nakhlites?

Abstract— Considerable evidence points to a martian origin of the SNC meteorites. Noble gas isotopic compositions have been measured in most SNC meteorites. The ¹²⁹Xe/¹³²Xe vs. ⁸⁴Kr/¹³²Xe ratios in Chassigny, most shergottites, and lithology C of EETA 79001 define a linear array. This array is thought to be a mixing line between martian mantle and martian atmosphere. One of the SNC meteorites, Nakhla, contains a leachable component that has an elevated ¹²⁹Xe/¹³²Xe ratio relative to its ⁸⁴Kr/¹³²Xe ratio when compared to this approximately linear array. The leachable component probably consists in part of iddingsite, an alteration product produced by interaction of olivine with aqueous fluid at temperatures lower than 150 °C. The elevated Xe isotopic ratio may represent a distinct reservoir in the martian crust or mantle. More plausibly, it is elementally fractionated martian atmosphere. Formation of sediments fractionates the noble gases in the correct direction. The range of sediment/atmosphere fractionation factors is consistent with the elevated ¹²⁹Xe/¹³²Xe component in Nakhla being contained in iddingsite, a low temperature weathering product. The crystallization age of Nakhla is 1.3 Ga. Its low-shock state suggests that it was ejected from near the surface of Mars. As liquid water is required for the formation of iddingsite, these observations provide further evidence for the near surface existence of aqueous fluids on Mars more recently than 1.3 Ga.     

Ion microprobe U‐Th‐Pb dating and REE analyses of phosphates in the nakhlites Lafayette and Yamato‐000593/000749

Abstract— U, Th, and Pb isotopes and rare earth elements (REEs) in individual phosphate grains from martian meteorites Lafayette and Yamato‐000593/000749 were measured using a sensitive high‐resolution ion microprobe (SHRIMP). Observed U‐Pb data of 12 apatite grains from Yamato (Y‐) 000593/000749 are well represented by linear regressions in both “conventional” 2D isochron plots and the 3D U‐Pb plot (total Pb/U isochron), indicating that the formation age of this meteorite is 1.53 ± 0.46 Ga (2σ). On the other hand, the data of nine apatite grains from Lafayette are well represented by planar regression rather than linear regression, indicating that its formation age is 1.15 ± 0.34 Ga (2σ) and that a secondary alteration process slightly disturbed its U‐Pb systematics as discussed in the literature regarding Nakhla. The observed REE abundance patterns of the apatites in Lafayette and Yamato‐000749, normalized to CI chondrites, are characterized by a progressive depletion of heavy REEs (HREEs), a negative Eu anomaly, similarity to each other, and consistency with previously reported data for Nakhla. Considering the extensive data from other radiometric systems such as Sm‐Nd, Rb‐Sr, Ar‐Ar, and trace elements, our results suggest that the parent magmas of the nakhlites, including the newly found Y‐000593/000749, are similar and that their crystallization ages are ?1.3 Ga.     

Experimental hydrothermal alteration of a martian analog basalt: Implications for martian meteorites

Abstract— A number of martian meteorite samples contain secondary alteration minerals such as Ca‐Mg‐Fe carbonates, Fe oxides, and clay minerals. These mineral assemblages hint at hydrothermal processes occurring in the martian crust, but the alteration conditions are poorly constrained. This study presents the results of experiments that examined the alteration of a high‐Fe basalt by CO₂‐saturated aqueous fluids at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C and water‐rock ratios of 1:1 and 1:10. Results indicate that observable alteration of the basalt takes place after runs of only seven days. This alteration includes mobilization of silica into phases such as opal‐CT and quartz, as well as the formation of carbonates, oxides, and at some conditions, zeolites and hydrous silicates. The degree of alteration increases with run temperature and, in high‐temperature vapor experiments, with increasing water content of the vapor. The degree of alteration and the mineralogy observed in the martian meteorites suggests that none of these samples were exposed to aqueous fluids for long periods of time. Nakhla and Lafayette probably interacted with water for relatively brief periods of time; if so, silica may have been leached from the parent rocks by the altering fluids. Allan Hills 84001 shows possible evidence for very limited interaction with an aqueous fluid, but the overall slight degree of alteration described for this meteorite strongly suggests that it never interacted extensively or at high temperature with any water‐bearing fluid. Elephant Moraine A79001 may not have been altered by aqueous fluids at all. The results of this study best support models wherein the meteorite parent rocks were wetted intermittently or for brief periods of time rather than models that invoke long‐term reaction with large volumes of water. Our experiments studied alteration of a high‐Fe basalt by dilute, CO₂‐saturated, aqueous solutions at 23 and 75 °C and by mixed H₂O‐CO₂ vapors at 200 and 400 °C. The results suggest that alteration of the parent rock takes place even after very short reaction times of seven days. All experiments produced carbonate minerals, including calcite, and in some cases, magnesite, siderite, and ankerite. A free silica phase, either opal, quartz, or hydrated silica, formed in most experiments. More altered experiments also contained minerals such as zeolites and hydrous phyllosilicates. Clay minerals were not observed to form in any experiments. In aqueous fluids, higher temperature corresponded with a higher degree of alteration, whereas changing fluid composition had no observable effect. In high‐temperature vapors, the degree of alteration was controlled by temperature and the proportion of H₂O to CO₂, with water‐rock ratio also playing a role in transport of silica. Application of these results to martian meteorites that contain secondary alteration minerals suggests that none of the martian rocks underwent extensive interaction with aqueous fluids. Nakhla and Lafayette contain clay minerals, which suggests that they interacted with water to some extent, possibly at elevated temperatures. Although ALH84001 shows possible evidence of very limited interaction with aqueous fluids, EETA79001 does not. These results support models for the alteration of these meteorites that do not invoke long‐term interaction with water or reaction with large volumes of water. Except for some models for alteration of ALH84001, this conclusion agrees with most of the literature on alteration of martian meteorites.     

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.     

Ejection ages from krypton‐81‐krypton‐83 dating and pre‐atmospheric sizes of martian meteorites

Abstract— Cosmic‐ray exposure (CRE) ages and Mars ejection times were calculated from the radionuclide ⁸¹Kr and stable Kr isotopes for seven martian meteorites. The following ⁸¹Kr‐Kr CRE ages were obtained: Los Angeles = 3.35 ± 0.70 Ma; Queen Alexandra Range 94201 = 2.22 ± 0.35 Ma; Shergotty = 3.05 ± 0.50 Ma; Zagami = 2.98 ± 0.30 Ma; Nakhla = 10.8 ± 0.8 Ma; Chassigny = 10.6 ± 2.0 Ma; and Allan Hills 84001 = 15.4 ± 5.0 Ma. Comparison of these ages with previously obtained CRE ages from the stable noble gas nuclei ³He, ²¹Ne, and ³⁸Ar shows excellent agreement. This indicates that the method for the production rate calculation for the stable nuclei is reliable. In all martian meteorites we observe effects induced by secondary cosmic‐ray produced epithermal neutrons. Epithermal neutron fluxes, φ_n (30–300 eV), are calculated based on the reaction ⁷⁹Br(n, γβ)⁸⁰Kr. We show that the neutron capture effects were induced in free space during Mars‐Earth transfer of the meteoroids and that they are not due to a pre‐exposure on Mars before ejection of the meteoritic material. Neutron fluxes and slowing down densities experienced by the meteoroids are calculated and pre‐atmospheric sizes are estimated. We obtain minimum radii in the range of 22–25 cm and minimum masses of 150–220 kg. These results are in good agreement with the mean sizes reported for model calculations using current semiempirical data.     

Launch of martian meteorites in oblique impacts

A high-velocity oblique impact into the martian surface accelerates solid target material to escape velocity. A fraction of that material eventually falls as meteorites on Earth. For a long time they were called the SNC meteorites (Shergotty, Nakhla, and Chassigny). We study production of potential martian meteorites numerically within the frame of 3D hydrodynamic modeling. The ratio of the volume of escaping solid ejecta to projectile volume depends on the impact angle, impact velocity and the volatile content in the projectile and in the target. The size distribution of ejected fragments appears to be of crucial importance for the atmosphere-ejecta interaction in the case of a relatively small impact (with final crater size <3 km): 10-cm-sized particles are decelerated efficiently, while 30-50% of larger fragments could escape Mars. The results of numerical modeling are compared with shock metamorphic features in martian meteorites, their burial depth, and preatmospheric mass. Although it is impossible to accelerate ejected fragments to escape velocity without substantial compression (above 10 GPa), the maximum temperature increase in dunite (Chassigny) or ortopyroxenite (ALH84001) may be lower than 200 degree. This result is consistent with the observed chaotic magnetization of ALH84001. The probability of microbes' survival may be rather high even for the extreme conditions during the ejection process.     

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.     

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.     

Replacement of glass in the Nakhla meteorite by berthierine: Implications for understanding the origins of aluminum‐rich phyllosilicates on Mars

A scanning and transmission electron microscope study of aluminosilicate glasses within melt inclusions from the Martian meteorite Nakhla shows that they have been replaced by berthierine, an aluminum‐iron serpentine mineral. This alteration reaction was mediated by liquid water that gained access to the glasses along fractures within enclosing augite and olivine grains. Water/rock ratios were low, and the aqueous solutions were circumneutral and reducing. They introduced magnesium and iron that were sourced from the dissolution of olivine, and exported alkalis. Berthierine was identified using X‐ray microanalysis and electron diffraction. It is restricted in its occurrence to parts of the melt inclusions that were formerly glass, thus showing that under the ambient physico‐chemical conditions, the mobility of aluminum and silicon were low. This discovery of serpentine adds to the suite of postmagmatic hydrous silicates in Nakhla that include saponite and opal‐A. Such a variety of secondary silicates indicates that during aqueous alteration compositionally distinct microenvironments developed on sub‐millimeter length scales. The scarcity of berthierine in Nakhla is consistent with results from orbital remote sensing of the Martian crust showing very low abundances of aluminum‐rich phyllosilicates.     

Volatile compounds in shergottite and nakhlite meteorites

Abstract— Vacuum pyrolysis and quadrupole mass spectrometry were used to measure evolved-gas profiles and total concentrations of H₂O, CO₂, CO, SO₂, S₂, H₂S, HCl, Cl, and hydrocarbons in both exterior and interior samples of shergottites (ALHA77005, EETA79001, and Shergotty), a nakhlite (Nakhla), and eucrites (ALHA81001, EETA79004, and Pasamonte). Eucrites were analyzed as control samples to monitor effects of terrestrial weathering and contamination, relative to properties sought for the shergottite-nakhlite parent body. In contrast with eucrites, shergottites and Nakhla contain large proportions of their sulfur as oxidized sulfur compounds. Sulfate occurs in all shergottite and Nakhla samples and carbonate was confirmed in EETA79001 and Nakhla. Carbonate and sulfate abundances are inversely correlated but total chlorine abundance varies directly with fractional sulfate abundance. Most of the volatile compounds seem to be anhydrous, based on low bulk water contents in the meteorites (<0.1% H₂O), although Nakhla might contain significant water that is chemically associated with chlorine. Traces of saturated and unsaturated hydrocarbons in some samples are most likely terrestrial contaminants. The indigenous volatile compounds indicate that the shergottite-nakhlite parent body was highly oxidizing and supported aqueous geochemistry during at least part of its history.     

The oxygen fugacity of olivine‐phyric martian basalts and the components within the mantle and crust of Mars

Abstract— The oxygen fugacity of olivine‐phyric martian basalts is estimated using olivine‐pyroxene‐spinel equilibria, supported by detailed petrography. Results are plotted, along with previous oxygen fugacity estimates, against La/Yb, which is used as a proxy for long‐term incompatible‐element depletion or enrichment in martian basalt reservoirs. In general, the correlation between oxygen fugacity and La/Yb observed by Herd et al. (2002a) holds for the olivine‐phyric basalts. The implications of the correlation are re‐evaluated in light of work by Borg et al. (Forthcoming), which indicates that the variations in radiogenic isotopic composition can be modeled by mixing of mantle sources established by 4.5 Ga through crystallization of a magma ocean in lieu of assimilation of crustal material. The results demonstrate that the crust‐like component, interpreted as trapped liquid in a magma ocean cumulate pile, must be oxidized to explain the oxygen fugacity of the martian basalts. Consequently, the pre‐eruptive water contents of the more oxidized basalts are expected to be higher, although water is not called upon as the cause of the oxidation. Unmixing of mantle components provides an important context for the interpretation of oxygen isotopes, demonstrated here, and of samples returned from the martian surface.     

Micro Raman spectroscopy of amphiboles and pyroxenes in the martian meteorites Zagami and Lewis Cliff 88516

Abstract— We studied micro Raman spectroscopy of amphiboles and pyroxenes in the martian meteorites Zagami and Lewis Cliff (LEW) 88516. The obtained Raman spectra of the amphiboles are similar to those of kaersutite, reconfirming the previous studies that they are kaersutitic amphiboles enriched in Ca, Al, and Ti. Even though actinolite belongs to the same amphibole group (calcic amphibole) as kaersutite, the Raman spectra of terrestrial actinolite are distinct from those of kaersutite, probably reflecting complex amphibole crystal structures. The Al‐Ti‐rich pyroxene observed in the magmatic inclusions within LEW 88516 olivine is compositionally similar to kaersutite but shows Raman spectra nearly identical to the regular pyroxene rather than amphibole. In contrast to amphibole, this will be due to relatively simple crystal structures of pyroxene. Thus, the Raman spectra of Al‐Ti‐rich phases in the martian meteorites are distinct between kaersutite and Al‐Ti‐rich pyroxene, and this study demonstrates that micro Raman spectroscopy is one of the best tools to perform mineralogical characterization of mineral phases in martian meteorites.     

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.     

Martian xenon components in Shergotty mineral separates: Locations,sources, and trapping mechanisms

Abstract— Isotopic signatures and concentrations of xenon have been measured in Shergotty mineral separates by laser step heating. Martian atmosphere and ‘martian interior’ xenon are present, as is a spallation component. Martian atmospheric xenon is 5–10 times more concentrated in opaque minerals (magnetite, ilmenite, and pyrrhotite) and maskelynite than in pyroxenes, perhaps reflecting grain size variation. This is shown to be consistent with shock incorporation. A component consisting of solar xenon with a fission contribution, similar to components previously identified in martian meteorites and associated with the martian interior, is best defined in the pyroxene‐dominated separates. This component exhibits a consistent ¹²⁹Xe (¹²⁹Xe/¹³²Xe ?1.2) excess over solar/planetary (¹²⁹Xe/¹³²Xe ?1.04). We suggest that gas present in the melt, perhaps a mixture of interior xenon and martian atmosphere, was incorporated into the pyroxenes in Shergotty as the minerals crystallized.     

A petrogenetic model for the origin and compositional variation of the martian basaltic meteorites

Abstract— The major element, trace element, and isotopic compositional ranges of the martian basaltic meteorite source regions have been modeled assuming that planetary differentiation resulted from crystallization of a magma ocean. The models are based on low to high pressure phase relationships estimated from experimental runs and estimates of the composition of silicate Mars from the literature. These models attempt to constrain the mechanisms by which the martian meteorites obtained their superchondritic CaO/Al₂O₃ ratios and their source regions obtained their parent/daughter (⁸⁷Rb/⁸⁶Sr, ¹⁴⁷Sm/¹⁴⁴Nd, and ¹⁷⁶Lu/¹⁷⁷Hf) ratios calculated from the initial Sr, Nd, and Hf isotopic compositions of the meteorites. High pressure experiments suggest that majoritic garnet is the liquidus phase for Mars relevant compositions at or above 12 GPa. Early crystallization of this phase from a martian magma ocean yields a liquid characterized by an elevated CaO/Al₂O₃ ratio and a high Mg#. Olivine‐pyroxene‐garnet‐dominated cumulates that crystallize subsequently will also be characterized by superchondritic CaO/Al₂O₃ ratios. Melting of these cumulates yields liquids with major element compositions that are similar to calculated parental melts of the martian meteorites. Furthermore, crystallization models demonstrate that some of these cumulates have parent/daughter ratios that are similar to those calculated for the most incompatible‐element‐depleted source region (i.e., that of the meteorite Queen Alexandra [QUE] 94201). The incompatible‐element abundances of the most depleted (QUE 94201‐like) source region have also been calculated and provide an estimate of the composition of depleted martian mantle. The incompatible‐element pattern of depleted martian mantle calculated here is very similar to the pattern estimated for depleted Earth's mantle. Melting the depleted martian mantle composition reproduces the abundances of many incompatible elements in the parental melt of QUE 94201 (e.g., Ba, Th, K, P, Hf, Zr, and heavy rare earth elements) fairly well but does not reproduce the abundances of Rb, U, Ta and light rare earth elements. The source regions for meteorites such as Shergotty are successfully modeled as mixtures of depleted martian mantle and a late stage liquid trapped in the magma ocean cumulate pile. Melting of this hybrid source yields liquids with major element abundances and incompatible‐element patterns that are very similar to the Shergotty bulk rock.