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.     

Trace elements in olivine and the petrogenesis of the intermediate,olivine‐phyric shergottite NWA 10170

Olivine‐phyric shergottites represent primitive basaltic to picritic rocks, spanning a large range of Mg# and olivine abundances. As primitive olivine‐bearing magmas are commonly representative of their mantle source on Earth, understanding the petrology and evolution of olivine‐phyric shergottites is critical in our understanding of Martian mantle compositions. We present data for the olivine‐phyric shergottite Northwest Africa (NWA) 10170 to constrain the petrology with specific implications for magma plumbing‐system dynamics. The calculated oxygen fugacity and bulk‐rock REE concentrations (based on modal abundance) are consistent with a geochemically intermediate classification for NWA 10170, and overall similarity with NWA 6234. In addition, we present trace element data using laser ablation ICP‐MS for coarse‐grained olivine cores, and compare these data with terrestrial and Martian data sets. The olivines in NWA 10170 contain cores with compositions of Fo₇₇ that evolve to rims with composition of Fo₅₈, and are characterized by cores with low Ni contents (400–600 ppm). Nickel is compatible in olivine and such low Ni content for olivine cores in NWA 10170 suggests either early‐stage fractionation and loss of olivine from the magma in a staging chamber at depth, or that Martian magmas have lower Ni than terrestrial magmas. We suggest that both are true in this case. Therefore, the magma does not represent a primary mantle melt, but rather has undergone 10–15% fractionation in a staging chamber prior to extrusion/intrusion at the surface of Mars. This further implies that careful evaluation of not only the Mg# but also the trace element concentrations of olivine needs to be conducted to evaluate pristine mantle melts versus those that have fractionated olivine (±pyroxene and oxide minerals) in staging chambers.     

Experimental petrology of the Tissint meteorite: Redox estimates,crystallization curves,and evaluation of petrogenetic models

Tissint is an olivine‐phyric shergottite from an incompatible element depleted Martian mantle source. Oxythermobarometry applied to Tissint mineral phases demonstrates that the Tissint magma underwent an increase in oxygen fugacity, from ~3.5 log units below the quarz‐fayalite‐magnetite (QFM ) buffer during the early stages of crystallization, to QFM ?1.4 during the latter stages. This is the first time that such an oxidation event has been observed in a depleted shergottite. The reason for the oxidation event is unclear; however, calculations using the MELTS thermodynamic model suggest that auto‐oxidation is insufficient to cause more than ~1 log unit of oxidation, and therefore an external oxidation mechanism—such as oxidation by degassing—is required. If volatiles are responsible for the oxidation, then it indicates that volatiles are not exclusively tied to the enriched Martian mantle reservoir. A series of experiments using the Tissint parental magma were carried out under fixed (isothermal) or variable (cooling rate) temperature control, and at either reducing (QFM ?3.2) or oxidizing (QFM ?1) redox conditions. The observed liquid line of descent supports a potential genetic relationship between basaltic shergottites and olivine‐phyric shergottites. A peritectic relation where olivine is resorbed to form pyroxene is favored by increased oxygen fugacity; if oxidation during crystallization is more common than presently believed, it may explain why olivine is typically anhedral in olivine‐phyric shergottites. Results from a cooling‐rate experiment in which the oxygen fugacity was changed during the latter stages of crystallization resulted in olivine with a Cr compositional profile consistent with oxidized isothermal experiments, despite forming primarily under reducing conditions. A similar profile is observed in Tissint olivines, consistent with its redox history. Our results provide insights into the potential influence of oxidation events on the compositional zoning of minor or trace elements in olivine in olivine‐phyric basalts.     

Martian meteorite Tissint records unique petrogenesis among the depleted shergottites

Tissint, a new unaltered piece of Martian volcanic materials, is the most silica‐poor and Mg‐Fe‐rich igneous rock among the “depleted” olivine‐phyric shergottites. Fe‐Mg zoning of olivine suggests equilibrium growth (<0.1 °C h^?1) in the range of Fo_80–56 and olivine overgrowth (Fo_55–18) through a process of rapid disequilibrium (~1.0–5.0 °C h^?1). The spatially extended (up to 600 μm) flat‐top Fe‐Mg profiles of olivine indicates that the early‐stage cooling rate of Tissint was slower than the other shergottites. The chemically metastable outer rim of olivine (55) consists of oscillatory phosphorus zoning at the impact‐induced melt domains and grew rapidly compared to the early to intermediate‐stage crystallization of the Tissint bulk. High‐Ca pyroxene to low‐Ca pyroxene and high‐Ca pyroxene to plagioclase ratios of Tissint are more comparable to the enriched basaltic and enriched olivine‐phyric shergottites. Dominance of augite over plagioclase induced augite to control the Ca‐buffer in the residual melt suppressing the plagioclase crystallization, which also caused a profound effect on the Al‐content in the late‐crystallized pyroxenes. Mineral chemical stability, phase‐assemblage saturation, and pressure–temperature path of evolution indicates that the parent magma entered the solidus and left the liquidus field at a depth of 40–80 km in the upper mantle. Petrogenesis of Tissint appears to be similar to LAR 06319, an enriched olivine‐phyric shergottite, during the early to intermediate stage of crystallization. A severe shock‐induced deformation resulted in remelting (10–15 vol%), recrystallization (most Fe‐rich phases), and exhumation of Tissint in a time scale of 1–8 yr. Tissint possesses some distinct characteristics, e.g., impact‐induced melting and deformation, forming phosphorus‐rich recrystallization rims of olivine, and shock‐induced melt domains without relative enrichment of LREEs compared to the bulk; and shared characteristics, e.g., modal composition and magmatic evolution with the enriched basaltic shergottites, evidently reflecting unique mantle source in comparison to the clan of the depleted members.     

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.     

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%.     

Mineral chemistry of the Tissint meteorite: Indications of two‐stage crystallization in a closed system

The Tissint meteorite is a geochemically depleted, olivine‐phyric shergottite. Olivine megacrysts contain 300–600 μm cores with uniform Mg# (~80 ± 1) followed by concentric zones of Fe‐enrichment toward the rims. We applied a number of tests to distinguish the relationship of these megacrysts to the host rock. Major and trace element compositions of the Mg‐rich core in olivine are in equilibrium with the bulk rock, within uncertainty, and rare earth element abundances of melt inclusions in Mg‐rich olivines reported in the literature are similar to those of the bulk rock. Moreover, the P Kα intensity maps of two large olivine grains show no resorption between the uniform core and the rim. Taken together, these lines of evidence suggest the olivine megacrysts are phenocrysts. Among depleted olivine‐phyric shergottites, Tissint is the first one that acts mostly as a closed system with olivine megacrysts being the phenocrysts. The texture and mineral chemistry of Tissint indicate a crystallization sequence of: olivine (Mg# 80 ± 1) → olivine (Mg# 76) + chromite → olivine (Mg# 74) + Ti‐chromite → olivine (Mg# 74–63) + pyroxene (Mg# 76–65) + Cr‐ulvöspinel → olivine (Mg# 63–35) + pyroxene (Mg# 65–60) + plagioclase, followed by late‐stage ilmenite and phosphate. The crystallization of the Tissint meteorite likely occurred in two stages: uniform olivine cores likely crystallized under equilibrium conditions; and a fractional crystallization sequence that formed the rest of the rock. The two‐stage crystallization without crystal settling is simulated using MELTS and the Tissint bulk composition, and can broadly reproduce the crystallization sequence and mineral chemistry measured in the Tissint samples. The transition between equilibrium and fractional crystallization is associated with a dramatic increase in cooling rate and might have been driven by an acceleration in the ascent rate or by encounter with a steep thermal gradient in the Martian crust.     

The variability of ruthenium in chromite from chassignite and olivine‐phyric shergottite meteorites: New insights into the behavior of PGE and sulfur in Martian magmatic systems

The Martian meteorites comprise mantle‐derived mafic to ultramafic rocks that formed in shallow intrusions and/or lava flows. This study reports the first in situ platinum‐group element data on chromite and ulvöspinel from a series of dunitic chassignites and olivine‐phyric shergottites, determined using laser‐ablation ICP‐MS. As recent studies have shown that Ru has strongly contrasting affinities for coexisting sulfide and spinel phases, the precise in situ analysis of this element in spinel can provide important insights into the sulfide saturation history of Martian mantle‐derived melts. The new data reveal distinctive differences between the two meteorite groups. Chromite from the chassignites Northwest Africa 2737 (NWA 2737) and Chassigny contained detectable concentrations of Ru (up to ~160 ppb Ru) in solid solution, whereas chromite and ulvöspinel from the olivine‐phyric shergottites Yamato‐980459 (Y‐980459), Tissint, and Dhofar 019 displayed Ru concentrations consistently below detection limit (<42 ppb). The relatively elevated Ru signatures of chromite from the chassignites suggest a Ru‐rich (~1–4 ppb) parental melt for this meteorite group, which presumably did not experience segregation of immiscible sulfide liquids over the interval of mantle melting, melt ascent, and chromite crystallization. The relatively Ru‐depleted signature of chromite and ulvöspinel from the olivine‐phyric shergottites may be the consequence of relatively lower Ru contents (<1 ppb) in the parental melts, and/or the presence of sulfides during the crystallization of the spinel phases. The results of this study illustrate the significance of platinum‐group element in situ analysis on spinel phases to decipher the sulfide saturation history of magmatic systems.     

Water undersaturated mantle plume volcanism on present‐day Mars

Based on meteorite evidence, the present‐day Martian mantle has a combined abundance of up to a few hundred ppm of H₂O, Cl, and F, which lowers the solidus and enhances the magma production rate. Adiabatic decompression melting in upwelling mantle plumes is the best explanation for young (last 200 Myr) volcanism on Mars. We explore water undersaturated mantle plume volcanism using a finite element mantle convection model coupled to a model of hydrous peridotite melting. Relative to a dry mantle, the reduction in solidus temperature due to water increases the magma production rate by a factor of 1.3–1.7 at 50 ppm water and by a factor of 1.9–3.2 at 200 ppm water. Mantle water also decreases the viscosity and increases the vigor of convection, which indirectly increases the magma production rate by thinning the thermal boundary layer and increasing the flow velocity. At conditions relevant to Mars, these indirect effects can cause an order of magnitude increase in the magma production rate. Using geologic and geophysical observations of the Late Amazonian magma production rate and geochemical observations of melt fractions in shergottite meteorites, present‐day Mars is constrained to have a core–mantle boundary temperature of ~1750 to 1800 °C and a volume‐averaged thermal Rayleigh number of 2 × 10⁶ to 10⁷, indicating that moderately vigorous mantle convection has persisted to the present day. Melting occurs at depths of 2.5–6 GPa and is controlled by the Rayleigh number at the low pressure end and by the mantle water concentration at high pressure.     

Two‐stage polybaric formation of the new enriched,pyroxene‐oikocrystic,lherzolitic shergottite,NWA 7397

Northwest Africa (NWA) 7397 is a newly discovered, enriched, lherzolitic shergottite, the third described example of this group. This meteorite consists of two distinct textural lithologies (1) poikilitic—comprised of zoned pyroxene oikocrysts, with chadacrysts of chromite and olivine, and (2) nonpoikilitic—comprised of olivine, low‐Ca and high‐Ca pyroxene, maskelynite, and minor abundances of merrillite, spinel, ilmenite, and pyrrhotite. The constant Ti/Al ratios of pyroxene oikocrysts suggests initial crystallization of the poikilitic lithology at depth (equivalent to pressures of approximately 10 kbar), followed by crystallization of the nonpoikilitic lithology at shallower levels. Oxygen fugacity conditions become more oxidizing during crystallization ranging from fO₂ conditions of approximately QFM‐2 to QFM‐0.7. Magma calculated to be in equilibrium with the major rock‐forming minerals is LREE‐enriched relative to depleted or intermediate shergottites and has flat overall profiles. Therefore, we suggest that the parental magma for NWA 7397 had sampled an enriched, oxidized, Martian geochemical source, similar to that of other enriched basaltic and olivine‐phyric shergottites. We present a polybaric formation model for the lherzolitic shergottite NWA 7397, to account for the petrologic constraints. Three successive stages in the development of NWA 7397 are discussed (1) formation of a REE‐enriched parental magma from a distinct Martian mantle reservoir; (2) magma ponding and development of a staging chamber concomitant with initial crystallization of the poikilitic lithology; and (3) magma ascent to the near surface, with entrainment of cumulates from the staging chamber and subsequent crystallization of the nonpoikilitic lithology en route to the surface.     

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.     

An experimental study of partial melting and fractional crystallization on the HED parent body

We have performed an experimental and modeling study of the partial melting behavior of the HED parent body and of the fractional crystallization of liquids derived from its mantle. We estimated the mantle composition by assuming chondritic ratios of refractory lithophile elements, adjusting the Mg# and core size to match the density and moment of inertia of Vesta, and the compositions of Mg‐rich olivines found in diogenites. The liquidus of a mantle with Mg# (=100*[Mg/(Mg+Fe)]) 80 is ~1625 °C and, under equilibrium conditions, the melt crystallizes olivine alone until it is joined by orthopyroxene at 1350 °C. We synthesized the melt from our 1350 °C experiment and simulated its fractional crystallization path. Orthopyroxene crystallizes until it is replaced by pigeonite at 1200 °C. Liquids become eucritic and crystal assemblages resemble diogenites below 1250 °C. MELTS correctly predicts the olivine liquidus but overestimates the orthopyroxene liquidus by ~70 °C. Predicted melt compositions are in reasonable agreement with those generated experimentally. We used MELTS to determine that the range of mantle compositions that can produce eucritic liquids and diogenitic solids in a magma ocean model is Mg# 75–80 (with chondritic ratios of refractory elements). A mantle with Mg# ~ 70 can produce eucrites and diogenites through sequential partial melting.     

Grove Mountains 020090 enriched lherzolitic shergottite: A two‐stage formation model

Grove Mountains (GRV) 020090 is an enriched lherzolitic shergottite, distinct from other lherzolitic shergottites, except RBT 04262/1. Its characteristics include high abundance of plagioclase (24.2 vol% in the nonpoikilitic area), presence of K‐feldspar, common occurrence of baddeleyite, high FeO contents of olivine (bimodal peaks at Fa 33 mol% and Fa 41 mol%) and low‐Ca pyroxenes (bimodal peaks at Fs 23.8–31.7 mol% and Fs 25.7–33.9 mol%), and significant LREE enrichment of phosphates (500–610 × CI). The bulk composition of GRV 020090 suggests derivation from partial melting of an enriched reservoir. However, the REE patterns of the cores of pigeonite oikocrysts and the olivine chadacrysts are indistinguishable from those of GRV 99027 and other moderately depleted lherzolitic shergottites, and reveal a LREE‐depleted pattern of the primordial parent magma. We propose that the primordial parent magma of GRV 020090 was derived from a moderately depleted Martian upper mantle reservoir, and later the residual melt was contaminated by oxidized and enriched Martian crustal materials as it ascended up to the subsurface. GRV 020090 and RBT 04262/1 may have sampled an igneous unit different from other lherzolitic shergottites.     

Petrogenesis of the Dar al Gani (DaG) 1.1 Ma ejection-paired olivine-phyric shergottites and implications for ~470 Ma Martian volcanism

The Dar al Gani (DaG) olivine-phyric shergottites share mineralogical and geochemical characteristics, which confirm that these meteorites are derived from a single source. Bulk trace elements (La/Yb—0.12), in situ maskelynite ⁸⁷Sr/⁸⁶Sr (~0.7014) and redox estimates (FMQ ~ −2) indicate derivation from a depleted, reduced mantle reservoir; identical to all ~470 Ma shergottites ejected at 1.1 Ma. The DaG shergottites have been variably affected by terrestrial alteration, which precipitated carbonate along fractures and modified bulk-rock fluid mobile (e.g., Ba) elements. Nonetheless, sufficient data are available to construct a multi-stage formation model for the DaG shergottites and other 1.1 Ma ejection-paired shergottites that erupted at ~470 Ma. First, partial melting of a depleted mantle source occurred at 1540 ± 20°C and 1.2 ± 0.1 GPa, equivalent to > ~100 km depth. Then, initial crystallization in a staging chamber at ~85 km depth at the crust–mantle boundary took place, followed by magma evolution and variable incorporation of antecrystic olivine ± orthopyroxene. Subsequently, crystallization of olivine phenocrysts and re-equilibration of olivine antecrysts occurred within an ascending magma. Finally, magmas with variable crystal loads erupted at the surface, where varied cooling rates produced a range of groundmass textures. This model is similar to picritic flood basalt magmas erupted on Earth.     

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.     

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.     

Highly siderophile element (HSE) abundances in the mantle of Mars are due to core formation at high pressure and temperature

Highly siderophile elements (HSEs) can be used to understand accretion and core formation in differentiated bodies, due to their strong affinity for FeNi metal and sulfides. Coupling experimental studies of metal–silicate partitioning with analyses of HSE contents of Martian meteorites can thus offer important constraints on the early history of Mars. Here, we report new metal–silicate partitioning data for the PGEs and Au and Re across a wide range of pressure and temperature space, with three series designed to complement existing experimental data sets for HSE. The first series examines temperature effects for D(HSE) in two metallic liquid compositions—C‐bearing and C‐free. The second series examines temperature effects for D(Re) in FeO‐bearing silicate melts and FeNi‐rich alloys. The third series presents the first systematic study of high pressure and temperature effects for D(Au). We then combine our data with previously published partitioning data to derive predictive expressions for metal–silicate partitioning of the HSE, which are subsequently used to calculate HSE concentrations of the Martian mantle during continuous accretion of Mars. Our results show that at midmantle depths in an early magma ocean (equivalent to approximately 14 GPa, 2100 °C), the HSE contents of the silicate fraction are similar to those observed in the Martian meteorite suite. This is in concert with previous studies on moderately siderophile elements. We then consider model calculations that examine the role of melting, fractional crystallization, and sulfide saturation/undersaturation in establishing the range of HSE contents in Martian meteorites derived from melting of the postcore formation mantle. The core formation modeling indicates that the HSE contents can be established by metal–silicate equilibrium early in the history of Mars, thus obviating the need for a late veneer for HSE, and by extension volatile siderophile elements, or volatiles in general.     

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.     

Crystallization experiments on a Gusev Adirondack basalt composition

Abstract— Until recently, the SNC meteorites represented the only source of information about the chemistry and petrology of the Martian surface and mantle. The Mars Exploration Rovers have now analyzed rocks on the Martian surface, giving additional insight into the petrology and geochemistry of the planet. The Adirondack basalts, analyzed by the MER Spirit in Gusev crater, are olivine‐phyric basaltic rocks which have been suggested to represent liquids, and might therefore provide new insights into the chemistry of the Martian mantle. Experiments have been conducted on a synthetic Humphrey composition at upper mantle and crustal conditions to investigate whether this composition might represent a primary mantle‐derived melt. The Humphrey composition is multiply saturated at 12.5 kbar and 1375 °C with olivine and pigeonite; a primary anhydrous melt derived from a “chondritic” mantle would be expected to be saturated in orthopyroxene, not pigeonite. In addition, the olivine and pigeonite present at the multiple saturation are too ferroan to have been from a Martian mantle as is understood now. Therefore, it seems likely that the Humphrey composition does not represent a primary anhydrous melt from the Martian mantle, but was affected by mineral/melt fractionations at lower (crustal) pressures.