Synthesis of a spinifex‐textured basalt as an analog to Gusev crater basalts,Mars

Abstract– Analyses by the Mars Exploration Rover (MER), Spirit, of Martian basalts from Gusev crater show that they are chemically very different from terrestrial basalts, being characterized in particular by high Mg‐ and Fe‐contents. To provide suitable analog basalts for the International Space Analogue Rockstore (ISAR), a collection of analog rocks and minerals for preparing in situ space missions, especially, the upcoming Mars mission MSL‐2011 and the future international Mars‐2018 mission, it is necessary to synthesize Martian basalts. The aim of this study was therefore to synthesize Martian basalt analogs to the Gusev crater basalts, based on the geochemical data from the MER rover Spirit. We present the results of two experiments, one producing a quench‐cooled basalt (<1 h) and one producing a more slowly cooled basalt (1 day). Pyroxene and olivine textures produced in the more slowly cooled basalt were surprisingly similar to spinifex textures in komatiites, a volcanic rock type very common on the early Earth. These kinds of ultramafic rocks and their associated alteration products may have important astrobiological implications when associated with aqueous environments. Such rocks could provide habitats for chemolithotrophic microorganisms, while the glass and phyllosilicate derivatives can fix organic compounds.     

Report of the Working Party on the classification of the lunar igneous rocks

Abstract— A report is presented for a possible revised classification of lunar igneous rocks that still uses the division of Moon rocks into mare and highland types. It subdivides the mare rocks into basalts depending on TiO₂ content and glasses depending on colour, and subdivides the highland rocks principally into KREEP basalts and into coarse‐grained igneous rocks comparable to and using terrestrial igneous rock terminology.     

Similarities between the shergottites and terrestrial ferropicrites

Element abundance ratios have been used to both distinguish terrestrial and martian basalts and make estimates on the bulk planetary chemistry. However, these estimates are based upon ratios that are assumed to have been unaffected by igneous processes. Since the extent to which this is valid is unknown, comparisons of terrestrial and martian rocks are best conducted on rocks with similar mineralogy and petrology, and therefore a good likelihood of similar crystallization histories. When the geochemistry of terrestrial ferropicrites is compared with the olivine-phyric and basaltic shergottites, previously observed differences in chemistry are no longer definitive (i.e. Mg/Si, Al/Si, Ca/Si, Fe/Si, FeO/MnO, Al/Ti, Na/Ti, Na/Al, K/La, K/Rb, K/Th, K/U, Th/U ratios). Since ferropicrites are geochemical terrestrial analogs for the shergottites, their formation history can provide useful information about the formation of the shergottites. This suggests that both ferropicrites and shergottites formed from a heavily processed mantle source region.     

A new type of isotopic anomaly in shergottite sulfides

The isotopic composition and abundance of sulfur in extraterrestrial materials are of interest for constraining models of both planetary and solar system evolution. A previous study that included phase‐specific extraction of sulfur from 27 shergottites found the sulfur isotopic composition of the Martian mantle to be similar to that of terrestrial mid‐ocean ridge basalts, the Moon, and nonmagmatic iron meteorites. However, the presence of positive Δ³³S anomalies in igneous sulfides from several shergottites, indicating incorporation of atmospherically processed sulfur into the subsurface, complicated this interpretation. The current study expands upon the previous work through analyses of 20 additional shergottites, enabling tighter constraints on the isotopic composition of juvenile Martian sulfur. The updated composition (δ³⁴S = ?0.24 ± 0.05‰, Δ³³S = 0.0015 ± 0.0016‰, and Δ³⁶S = 0.039 ± 0.054‰, 2 s.e.m.), representing the weighted mean for all shergottites within the combined population of 47 without significant Δ³³S anomalies, strengthens our earlier result. The presence of sulfur isotopic anomalies in igneous sulfides of some meteorites suggests that their parent magmas may have assimilated crustal material. We observed small negative Δ³³S anomalies in sulfides from two meteorites, NWA 7635 and NWA 11300. Although negative Δ³³S anomalies have been observed in nakhlites and ALH 84001, previous anomalies in shergottites have all shown positive values of Δ³³S. Because NWA 7635 has formation age of 2.4 Ga and is much more ancient than shergottites analyzed previously, this finding expands our perspective on the continuity of Martian atmospheric sulfur photochemistry over geologic time.     

Mars regolith versus SNC meteorites: Possible evidence for abundant crustal carbonates

Viking XRF analyses of the Martian regolith are compared with typical igneous rocks of the Earth, the Moon, the eucrite parent asteroid, and especially the shergottites, nakhlites, and Chassigny (SNC) meteorites, which are suspected to be basalts and mafic cumulates from Mars. A striking feature of the Martian regolith, compared to igneous rocks with similar molar (Mg + Fe)/Si ratios, is its extraordinarily low Ca/Si ratio. The regolith's low Ca/Si ratio is probably not a result of simple mixing (isochemical weathering) of SNC-like rocks with other igneous rocks, unless the regolith contains a large component of rock with an improbable combination of extremely low Ca/Si and (Mg + Fe)/Si, and yet low K₂O and Zr. Several other models might conceivably account for the low Ca/Si ratio, but I suggest that most of the “missing” Ca was removed from the regolith as Ca-carbonate. Formation of a mass of carbonate equivalent to a global shell 20 m thick would suffice to remove 1000 mbar of CO₂ from the Martian atmosphere. Thus, the peculiar Ca/Si ratio of the Martian regolith tends to support the hypothesis that the climate of Mars was once far warmer and wetter than it is today.     

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

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

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%.     

Survival of microorganisms in smectite clays: implications for Martian exobiology

Manned exploration of Mars may result in the contamination of that planet with terrestrial microbes, a situation requiring assessment of the survival potential of possible contaminating organisms. In this study, the survival of Bacillius subtilis, Azotobacter chroococcum, and the enteric bacteriophage MS2 was examined in clays representing terrestrial (Wyoming type montmorillonite) or Martian (Fe(3+)-montmorillonite) soils exposed to terrestrial and Martian environmental conditions of temperature and atmospheric pressure and composition, but not to UV flux or oxidizing conditions. Survival of bacteria was determined by standard plate counts and biochemical and physiological measurements over 112 days. Extractable lipid phosphate was used to measure microbial biomass, and the rate of 14C-acetate incorporation into microbial lipids was used to determine physiological activity. MS2 survival was assayed by plaque counts. Both bacterial types survived terrestrial or Martian conditions in Wyoming montmorillonite better than Martian conditions in Fe(3+)-montmorillonite. Decreased survival may have been caused by the lower pH of the Fe(3+)-montmorillonite compared to Wyoming montmorillonite. MS2 survived simulated Mars conditions better than the terrestrial environment, likely due to stabilization of the virus caused by the cold and dry conditions of the simulated Martian environment. The survival of MS2 in the simulated Martian environment is the first published indication that viruses may be able to survive in Martian type soils. This work may have implications for planetary protection for future Mars missions.     

Small melt inclusions can record bulk magma compositions: A planetary example from the Martian basalt (shergottite) Tissint

Melt inclusions in igneous minerals can provide constraints on magma compositions, especially for planetary samples where mass is severely limited. Small inclusions (<15 μm diameter) are more abundant than large ones, but have been used little from concern that they did not entrap average magma, but are rich in melt of a diffusional layer against the host mineral. We compared bulk compositions and calculated original compositions of small and large melt inclusions in the Martian basalt meteorite (shergottite) Tissint. Small and large melt inclusions are consistent with the same line of igneous differentiation, have the same abundance ratios for incompatible elements (P, Ti, Al, K, Na), and are consistent with derivation from the bulk composition of Tissint (inferred to represent its parent melt composition). For Tissint, then, small melt inclusions show no evidence of entrapping diffusional boundary layers, and appear to have entrapped bulk magma. Thus, its small inclusions can be as useful as larger ones; this may be so for other planetary samples, and thus provides an additional tool for investigating planetary magmas.     

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.     

The rocks of Mars,from far and near

Abstract— The age, structure, composition, and petrogenesis of the martian lithosphere have been constrained by spacecraft imagery and remote sensing. How well do martian meteorites conform to expectations derived from this geologic context? Both data sets indicate a thick, extensive igneous crust formed very early in the planet's history. The composition of the ancient crust is predominantly basaltic, possibly andesitic in part, with sediments derived from volcanic rocks. Later plume eruptions produced igneous centers like Tharsis, the composition of which cannot be determined because of spectral obscuration by dust. Martian meteorites (except Allan Hills 84001) are inferred to have come from volcanic flows in Tharsis or Elysium, and thus are not petrologically representative of most of the martian surface. Remote‐sensing measurements cannot verify the fractional crystallization and assimilation that have been documented in meteorites, but subsurface magmatic processes are consistent with orbital imagery indicating thick crust and large, complex magma chambers beneath Tharsis volcanoes. Meteorite ejection ages are difficult to reconcile with plausible impact histories for Mars, and oversampling of young terrains suggests either that only coherent igneous rocks can survive the ejection process or that older surfaces cannot transmit the required shock waves. The mean density and moment of inertia calculated from spacecraft data are roughly consistent with the proportions and compositions of mantle and core estimated from martian meteorites. Thermal models predicting the absence of crustal recycling, and the chronology of the planetary magnetic field agree with conclusions from radiogenic isotopes and paleomagnetism in martian meteorites. However, lack of vigorous mantle convection, as inferred from meteorite geochemistry, seems inconsistent with their derivation from the Tharsis or Elysium plumes. Geological and meteoritic data provide conflicting information on the planet's volatile inventory and degassing history, but are apparently being reconciled in favor of a periodically wet Mars. Spacecraft measurements suggesting that rocks have been chemically weathered and have interacted with recycled saline groundwater are confirmed by weathering products and stable isotope fractionations in martian meteorites.     

Phase equilibrium investigations of the Adirondack class basalts from the Gusev plains,Gusev crater,Mars

Abstract— Phase equilibrium experiments have been performed on a synthetic analog of the Gusev plains basalt composition from the Spirit landing site on Mars. Near‐liquidus phase relations were determined over the pressure range of 0.1 to 1.5 GPa and at temperatures from 1125 to 1390 °C in a piston cylinder apparatus and 1 atm gas mixing furnace. The composition is multiply saturated with olivine, orthopyroxene, and spinel near its liquidus at 1320 °C and 1.0 GPa, or 85 km depth on Mars, placing an upper limit constraint on the thickness of the Martian lithosphere at the time of eruption. Our experimental work suggests that the Gusev basalts are anhydrous batch melts of a primitive Martian mantle similar to the composition estimated by Dreibus and Wänke (1984). The temperature of multiple saturation indicates the persistence of high mantle potential temperatures on Mars, similar to those on the modern Earth, until at least the very latest Noachian (3.7 Ga). These high mantle temperatures would be responsible for persistent basaltic volcanism throughout the southern highlands during the first billion years of Mars's history. The source for Gusev basalts differs strongly from the source for shergottite meteorites, reinforcing the idea of the absence of global mantle convection and mixing on Mars. The existence of a relatively primitive mantle reservoir requires that at least part of the mantle underwent little modification during early planetary differentiation.     

Martian basalt (shergottite) Queen Alexandra Range 94201 and lunar basalt 15555: A tale of two pyroxenes

Abstract— We present here ion microprobe analyses of rare earth and other selected trace and minor elements in pyroxenes of shergottite Queen Alexandra Range 94201 and lunar basalt 15555. Pyroxene zonation patterns record the crystallization histories of these two basaltic samples from Mars and the Moon, respectively, and allow a comparison of mafic melt evolution on these two planetary bodies. Elemental abundances and trends in pyroxenes of these two rocks indicate that their minerals formed by continuous, closed system fractional crystallization of their respective parent melts. This further supports the idea that QUE 94201 closely represents the composition of a true Martian basaltic melt (McSween et al., 1996). The main differences in pyroxene elemental zonation patterns in these two objects are attributed to earlier crystallization of whitlockite in QUE 94201 (i.e., before the Fe-rich pyroxenes) than in 15555 (after the Fe-rich pyroxenes). The size of Eu anomalies in pyroxenes of QUE 94201 is intermediate between that in pyroxenes of 15555 and the other shergottites and may imply that fO₂ conditions during crystallization of this Martian basalt were significantly more reducing than for other shergottites, although not quite as reducing as for lunar basalts. Cerium anomalies appear to be less prevalent in pyroxenes of QUE 94201 than other Antarctic shergottites and could be indicative of lesser degree of weathering in the Antarctic.     

K‐Ar dating of rocks on Mars: Requirements from Martian meteorite analyses and isochron modeling

Abstract— Radiometric age dating of Martian rocks and surfaces at known locations for which crater densities can be determined is highly desirable in order to fully understand Martian history. Performing K‐Ar age dating of igneous rocks on Mars by robots, however, presents technical challenges. Some of these challenges can be defined by examining Ar‐Ar data acquired on Martian meteorites, and others can be evaluated through numerical modeling of simulated K‐Ar isochrons like those that would be acquired robotically on Martian rocks. Excess ⁴⁰Ar is present in all shergottites. Thus for Martian rocks, the slopes of K‐Ar isochrons must be determined to reasonable precision in order to calculate reliable ages. Model simulations of possible isochrons give an indication of some requirements in order to define a precise rock age: Issues addressed here are: how many K‐Ar analyses should be made of rocks thought to have the same age; what range of K concentrations should these analyzed samples have; and what analytical uncertainty in K‐Ar measurements is desirable. Meteorite data also are used to determine the D/a² diffusion parameters for Ar in plagioclase and pyroxene separates of several shergottites and nakhlites. These data indicate the required temperatures and times for heating similar Martian rocks in order to extract Ar. Quantitatively extracting radiogenic ⁴⁰Ar could be difficult, and degassing cosmogenic Ar from mafic phases even more so. Considering all these factors, robotic K‐Ar dating of Martian rocks may be achievable, but will be challenging.     

Thermophysical properties of lunar material returned by Apollo missions

Data on thermophysical properties measured on lunar material returned by Apollo missions are reviewed. In particular, the effects of temperature and interstitial gaseous pressure on thermal conductivity and diffusivity have been studied. For crystalline rocks, breccias and fines, the thermal conductivity and diffusivity decrease as the interstitial gaseous pressure decreases from 1 atm to 10^–4T. Below 10^–4T, these properties become insensitive to the pressure. At a pressure of 10^–4T or below, the thermal conductivity of fines is more temperature dependent than that of crystalline rocks and breccias. The bulk density also affects the thermal conductivity of the fines. An empirical relationship between thermal conductivity, bulk density and temperature derived from the study of terrestrial material is shown to be consistent with the data on lunar samples. Measurement of specific heat shows that, regardless of the differences in mineral composition, crystalline rocks and fines have almost identical specific heat in the temperature range between 100 and 340K. The thermal parameter calculated from thermal conductivity, density and specific heat shows that the thermal properties estimated by earth-based observations are those characteristic only of lunar fines and not of crystalline rocks and breccias. The rate of radioactive heat generation calculated from the content of K, Th and U in lunar samples indicates that the surface layer of the lunar highland is more heat-producing than the lunar maria. This may suggest fundamental differences between the two regions.Now at Lamont-Doherty Geological Observatory, Columbia University, Palisades, New York, U.S.A.     

Basaltic glass as a habitat for microbial life: Implications for astrobiology and planetary exploration

Recent studies have demonstrated that terrestrial subaqueous basalts and hyaloclastites are suitable microbial habitats. During subaqueous basaltic volcanism, glass is produced by the quenching of basaltic magma upon contact with water. On Earth, microbes rapidly begin colonizing the glassy surfaces along fractures and cracks that have been exposed to water. Microbial colonization of basaltic glass leads to the alteration and modification of the rocks and produces characteristic granular and/or tubular bioalteration textures. Infilling of the alteration textures by minerals such as phyllosilicates, zeolites and titanite may enable their preservation through geologic time. Basaltic rocks are a major component of the Martian crust and are widespread on other solar system bodies. A variety of lines of evidence strongly suggests the long-term existence of abundant liquid water on ancient Mars. Recent orbiter, lander and rover missions have found evidence for the presence of transient liquid water on Mars, perhaps persisting to the present day. Many other solar system bodies, notably Europa, Enceladus and other icy satellites, may contain (or have once hosted) subaqueous basaltic glasses. The record of terrestrial glass bioalteration has been interpreted to extend as far back as ∼3.5 billion years ago and is widespread in oceanic crust and its metamorphic equivalents. The terrestrial record of glass bioalteration strongly suggests that glassy or formerly glassy basaltic rocks on extraterrestrial bodies that have interacted with liquid water are high-value targets for astrobiological exploration.     

Evidence for high‐temperature fractionation of lithium isotopes during differentiation of the Moon

Lithium isotope and abundance data are reported for Apollo 15 and 17 mare basalts and the LaPaz low‐Ti mare basalt meteorites, along with lithium isotope data for carbonaceous, ordinary, and enstatite chondrites, and chondrules from the Allende CV3 meteorite. Apollo 15 low‐Ti mare basalts have lower Li contents and lower δ⁷Li (3.8 ± 1.2‰; all uncertainties are 2 standard deviations) than Apollo 17 high‐Ti mare basalts (δ⁷Li = 5.2 ± 1.2‰), with evolved LaPaz mare basalts having high Li contents, but similar low δ⁷Li (3.7 ± 0.5‰) to Apollo 15 mare basalts. In low‐Ti mare basalt 15555, the highest concentrations of Li occur in late‐stage tridymite (>20 ppm) and plagioclase (11 ± 3 ppm), with olivine (6.1 ± 3.8 ppm), pyroxene (4.2 ± 1.6 ppm), and ilmenite (0.8 ± 0.7 ppm) having lower Li concentrations. Values of δ⁷Li in low‐ and high‐Ti mare basalt sources broadly correlate negatively with ¹⁸O/¹⁶O and positively with ⁵⁶Fe/⁵⁴Fe (low‐Ti: δ⁷Li ≤4‰; δ⁵⁶Fe ≤0.04‰; δ¹⁸O ≥5.7‰; high‐Ti: δ⁷Li >6‰; δ⁵⁶Fe >0.18‰; δ¹⁸O <5.4‰). Lithium does not appear to have acted as a volatile element during planetary formation, with subequal Li contents in mare basalts compared with terrestrial, martian, or vestan basaltic rocks. Observed Li isotopic fractionations in mare basalts can potentially be explained through large‐degree, high‐temperature igneous differentiation of their source regions. Progressive magma ocean crystallization led to enrichment in Li and δ⁷Li in late‐stage liquids, probably as a consequence of preferential retention of ⁷Li and Li in the melt relative to crystallizing solids. Lithium isotopic fractionation has not been observed during extensive differentiation in terrestrial magmatic systems and may only be recognizable during extensive planetary magmatic differentiation under volatile‐poor conditions, as expected for the lunar magma ocean. Our new analyses of chondrites show that they have δ⁷Li ranging between ?2.5‰ and 4‰. The higher δ⁷Li in planetary basalts than in the compilation of chondrites (2.1 ± 1.3‰) demonstrates that differentiated planetary basalts are, on average, isotopically heavier than most chondrites.     

Identification of a meteoritic component using chromium isotopic composition of impact rocks from the Lonar impact structure,India

The existence of mass‐independent chromium isotope variability of nucleosynthetic origin in meteorites and their components provides a means to investigate potential genetic relationship between meteorites and planetary bodies. Moreover, chromium abundances are depleted in most surficial terrestrial rocks relative to chondrites such that Cr isotopes are a powerful tool to detect the contribution of various types of extra‐terrestrial material in terrestrial impactites. This approach can thus be used to constrain the nature of the bolide resulting in breccia and melt rocks in terrestrial impact structures. Here, we report the Cr isotope composition of impact rocks from the ~0.57 Ma Lonar crater (India), which is the best‐preserved impact structure excavated in basaltic target rocks. Results confirm the presence of a chondritic component in several bulk rock samples of up to 3%. The impactor that created the Lonar crater had a composition that was most likely similar to that of carbonaceous chondrites, possibly a CM‐type chondrite.     

The chemical composition and structure of the moon

Three types of igneous rocks, all ultimately related to basaltic liquids, appear to be common on the lunar surface. They are: (1) iron-rich mare basalts, (2) U-, REE-, and Al-rich basalts (KREEP), and (3) plagioclase-rich or anorthositic rocks. All three rock types are depleted in elements more volatile than sodium and in the siderophile elements when relative element abundances are compared with those of carbonaceous chondrites. The chemistry and age relationships of these rocks suggest that they are derived from a feldspathic, refractory element-rich interior that becomes more pyroxenitic; that is, iron/magnesium-rich; with depth.It is suggested that the deeper parts of the lunar interior tend toward chondritic element abundances. The radial variation in mineralogy and bulk chemical composition inferred from the surface chemistry is probably a primitive feature of the Moon that reflects the accretion of refractory elementenriched materials late in the formation of the body.     

What we have learned about Mars from SNC meteorites

Abstract— The SNC meteorites are thought to be igneous martian rocks, based on their young crystallization ages and a close match between the composition of gases implanted in them during shock and the atmosphere of Mars. A related meteorite, ALH84001, may be older and thus may represent ancient martian crust. These petrologically diverse basalts and ultramafic rocks are mostly cumulates, but their parent magmas share geochemical and radiogenic isotopic characteristics that suggest they may have formed by remelting the same mantle source region at different times. Information and inferences about martian geology drawn from these samples include the following: Planetary differentiation occurred early at ～4.5 Ga, probably concurrently with accretion. The martian mantle contains different abundances of moderately volatile and siderophile elements and is more Fe-rich than that of the Earth, which has implications for its mineralogy, density, and origin. The estimated core composition has a S abundance near the threshold value for inner core solidification. The former presence of a core dynamo may be suggested by remanent magnetization in SNC meteorites, although these rocks may have been magnetized during shock. The mineralogy of martian surface units, inferred from reflectance spectra, matches that of basaltic shergottites, but SNC lithologies thought to have crystallized in the subsurface are not presently recognized. The rheological properties of martian magmas are more accurately derived from these meteorites than from observations of martian flow morphology, although the sampled range of magma compositions is limited. Estimates of planetary water abundance and the amount of outgassed water based on these meteorites are contradictory but overlap estimates based on geological observations and atmospheric measurements. Stable isotope measurements indicate that the martian hydrosphere experienced only limited exchange with the lithosphere, but it is in isotopic equilibrium with the atmosphere and has been since 1.3 Ga. The isotopically heavy atmosphere/hydrosphere composition deduced from these rocks reflects a loss process more severe than current atmospheric evolution models, and the occurrence of carbonates in SNC meteorites suggests that they, rather than scapolite or hydrous carbonates, are the major crustal sink for CO₂. Weathering products in SNC meteorites support the idea of limited alteration of the lithosphere by small volumes of saline, CO₂-bearing water. Atmospheric composition and evolution are further constrained by noble gases in these meteorites, although Xe and Kr isotopes suggest different origins for the atmosphere. Planetary ejection of these rocks has promoted an advance in the understanding of impact physics, which has been accomplished by a model involving spallation during large cratering events. Ejection of all the SNC meteorites (except ALH84001) in one or two events may provide a plausible solution to most constraints imposed by chronology, geochemistry, and cosmic ray exposure, although problems remain with this scenario; ALH84001 may represent older martian crust sampled during a separate impact.