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.     

Constraints on the structure of the martian interior determined from the chemical and isotopic systematics of SNC meteorites

Abstract— The crystallization ages of martian (SNC) meteorites give evidence that martian volcanism has continued until recent times‐perhaps until the present. These meteorites also indicate that the mantle source regions of this volcanism are modestly to extremely depleted by terrestrial standards. These 2 observations produce a conundrum. How is it that such depleted source regions have produced basaltic magma for such a long time? This contribution attempts to quantify the radiogenic heat production in 2 distinct martian mantle source regions: those of the shergottites and nakhlites. Compared to the depleted upper mantle of the Earth (MORB), the nakhlite source region is depleted by about a factor of 2, and the shergottite source region is depleted by a factor of 6. According to current geophysical models, the nakhlite source contains the minimum amount of radioactive heat production to sustain whole‐mantle convection and basalt generation over geologic time. A corollary of this conclusion is that the shergottite source contains much too little radioactivity to produce recent (<200 Ma) basalts. A model martian interior with a deep nakhlite mantle that is insulated by a shallow shergottite mantle may allow basalt production from both source regions if the divide between the nakhlite‐shergottite mantles acts as a thermal boundary layer. Similarities between lunar and martian isotopic reservoirs indicate that the Moon and Mars may have experienced similar styles of differentiation.     

Large‐ion lithophile element fractionation during the early differentiation of Mars and the composition of the martian primitive mantle

Abstract— Basaltic shergottites display a systematic decrease in K/Th, K/U, and K/La ratios with increasing K content. These trends are interpreted as mixing lines between relatively young martian magmas derived from highly depleted mantle sources and an ancient large‐ion lithophile (LIL) element‐enriched crustal component. One implication of this is that a substantial fractionation of these ratios occurs during the early crustal differentiation on Mars. Isotopic evidence from SNC meteorites and compositional data from Pathfinder and orbital gamma ray spectroscopy suggest that in excess of 50% of the LIL element complement of Mars resides in the crustal reservoir. If so, the primitive mantle of Mars is significantly more volatile‐depleted (i.e., lower K/Th, K/U, K/La) than previously thought but probably (though not necessarily) still less volatile‐depleted than the primitive mantle of the Earth. The La/Th ratios of virtually all SNC meteorites are subchondritic, including those with the most severe LREE‐depletion. Extrapolation of the basaltic shergottite trend suggests that both the depleted mantle end member and the enriched crustal end member have subchondritic La/Th ratios. This is in contrast with the Earth where basalts from LIL element‐depleted sources such as MORB have superchondritic La/Th ratios, complementary to the subchondritic ratios of the continental crust. Accordingly, assuming that the refractory elements are in chondritic proportions for the Mars primitive mantle, an additional major geochemical reservoir must exist on Mars that may not yet have been sampled.     

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.     

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.     

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.     

The early thermal evolution of Mars

Hf‐W isotopic systematics of Martian meteorites have provided evidence for the early accretion and rapid core formation of Mars. We present the results of numerical simulations performed to study the early thermal evolution and planetary scale differentiation of Mars. The simulations are confined to the initial 50 Myr (Ma) of the formation of solar system. The accretion energy produced during the growth of Mars and the decay energy due to the short‐lived radio‐nuclides ²⁶Al, ⁶⁰Fe, and the long‐lived nuclides, ⁴⁰K, ²³⁵U, ²³⁸U, and ²³²Th are incorporated as the heat sources for the thermal evolution of Mars. During the core‐mantle differentiation of Mars, the molten metallic blobs were numerically moved using Stoke's law toward the center with descent velocity that depends on the local acceleration due to gravity. Apart from the accretion and the radioactive heat energies, the gravitational energy produced during the differentiation of Mars and the associated heat transfer is also parametrically incorporated in the present work to make an assessment of its contribution to the early thermal evolution of Mars. We conclude that the accretion energy alone cannot produce widespread melting and differentiation of Mars even with an efficient consumption of the accretion energy. This makes ²⁶Al the prime source for the heating and planetary scale differentiation of Mars. We demonstrate a rapid accretion and core‐mantle differentiation of Mars within the initial ~1.5 Myr. This is consistent with the chronological records of Martian meteorites.     

Oxygen fugacity in the Martian mantle controlled by carbon: New constraints from the nakhlite MIL 03346

Abstract— Pyroxene structural data, along with analyses of titanomagnetite, fayalite and mesostasis of the new nakhlite Miller Range (MIL) 03346, define equilibration near 1 bar, 1100 °C, and oxygen fugacity near the FMQ buffer. There is a clear progression of oxygen fugacity (fO₂) in Martian meteorites from reduced Allan Hills (ALH) 84001 to intermediate shergottites to oxidized nakhlites. This trend can be explained by polybaric graphite‐CO‐CO₂ equilibria in the Martian mantle. Shergottites would have formed at pressures between 1.2 and 3.0 GPa, and nakhlite parent liquids formed at pressures >3.0 GPa, consistent with geochemical and petrologic data for the shergottites and nahklites. Carbon buffering in the Martian mantle could be responsible for variation in fO₂ in Martian meteorites (rather than assimilation or crustal interaction), as well as C‐H‐O fluids that could be the source of ˜30 ppb CH₄ detected by recent spacecraft missions. The conundrum of an oxidized current mantle and basalts, but reduced early mantle during core‐mantle equilibrium exists for both the Earth and Mars. A polybaric buffering role for graphite can explain this discrepancy for Mars, and thus it may not be necessary to have an oxidation mechanism like the dissociation of MgFe‐perovskite to account for the oxidized terrestrial mantle.     

Petrogenesis of the new lherzolitic shergottite Grove Mountains 99027: Constraints of petrography,mineral chemistry,and rare earth elements

Abstract— We report petrography, mineral chemistry, and microdistribution of rare earth elements (REE) in a new lherzolitic shergottite, Grove Mountains (GRV) 99027. The textural relationship and REE patterns of minerals suggest precipitation of cumulus olivine and chromite, followed by equilibrium crystallization of a closed system with a bulk composition of the inferred intercumulus melt. Subsolidus equilibrium temperatures of pyroxenes and olivine range from 1100 to 1210 °C, based on a two‐pyroxene thermometry and Ca partitioning between augite and olivine. Oxygen fugacity of the parent magma is 1.5–2.5 (av. 2.0 ± 0.4) log units below the quartz‐fayalite‐magnetite (QFM) buffer at 960–1360 °C, according to the olivine‐orthopyroxene‐chromite barometer. The ilmenite‐chromite barometer and thermometer show much wider ranges of oxygen fugacity (1.0–7.0 log unit below QFM) and temperature (1130–480 °C), suggesting subsolidus equilibration of the oxides at low temperatures, probably due to deep burial of GRV 99027 on Mars. The low oxygen fugacity and LREE depletion of the parent magma of GRV 99027 suggest low contamination by martian crust. Characteristics of GRV 99027 demonstrate similarity of lherzolitic shergottites, suggesting a high possibility of launch pairing or a homogeneous upper mantle of Mars if they were ejected by individual impact events. However, GRV 99027 probably experienced severe post‐shock thermal metamorphism in comparison with other lherzolitic shergottites, based on the re‐crystallization of maskelynite, the homogeneity of minerals, and the low subsolidus equilibrium temperatures between chromite and ilmenite.     

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.     

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.     

A petrologic and trace element study of Dar al Gani 476 and Dar al Gani 489: Twin meteorites with affinities to basaltic and lherzolitic shergottites

Abstract— We present the results of a combined mineralogic‐petrologic and ion microprobe study of two martian meteorites recently recovered in the Lybian Sahara, Dar al Gani 476 (DaG 476) and Dar al Gani 489 (DaG 489). Having resided in a hot desert environment for an extended time, DaG 476 and DaG 489 were subjected to terrestrial weathering that significantly altered their chemical composition. In particular, analyses of some of the silicates show light rare earth element (LREE)‐enrichment resulting from terrestrial alteration. In situ measurement of trace element abundances in minerals allows us to identify areas unaffected by this contamination and, thereby, to infer the petrogenesis of these meteorites. No significant compositional differences between DaG 476 and DaG 489 were found, supporting the hypothesis that they belong to the same fall. These meteorites have characteristics in common with both basaltic and lherzolitic shergottites, possibly suggesting spatial and petrogenetic associations of these two types of lithologies on Mars. However, the compositions of Fe‐Ti oxides and the size of Eu anomalies in the earliest‐formed pyroxenes indicate that the two Saharan meteorites probably experienced more reducing crystallization conditions than other shergottites (with the exception of Queen Alexandra Range (QUE) 94201). As is the case for other shergottites, trace element microdistributions in minerals of the DaG martian meteorites indicate that closed‐system crystal fractionation from a LREE‐depleted parent magma dominated their crystallization history. Furthermore, rare earth element abundances in the orthopyroxene megacrysts are consistent with their origin as xenocrysts rather than phenocrysts.     

Precursors of Mars: Constraints from nitrogen and oxygen isotopic compositions of martian meteorites

Abstract— We present an approach to assess the nature of materials involved in the accretion of Mars by the planet's nitrogen (δ¹⁵N) and oxygen (Δ¹⁷O) isotopic compositions as derived from data on martian meteorites. δ¹⁵N for Mars has been derived from nitrogen and xenon systematics, while Δ¹⁷O has been taken from the literature data. These signatures indicate that Mars has most probably accreted from enstatite and ordinary chondritic materials in a ratio of 74:26 and may not have a significant contribution from the carbonaceous (CI, CM, or CV) chondrites. This is consistent with the chromium isotopic (?⁵³Cr) signatures of martian meteorites and the bulk planet Fe/Si ratio for Mars as suggested by the moment of inertia factor (I/MR²) obtained from the Mars Pathfinder data. Further, a simple homogeneous accretion from the above two types of materials is found to be consistent with the planet's moment of inertia factor and the bulk composition of the mantle. But, it requires a core with 6.7 wt% Si, which is consistent with the new results from the high pressure and temperature melting experiments and chemical data on the opaque minerals in enstatite chondrites.     

The influence of mantle melting on the evolution of Mars

We present a parameterized convection model of Mars by incorporating a new heat-flow scaling law for stagnant-lid convection, to better understand how the evolution of Mars may be affected by mantle melting. Melting in the mantle during convection leads to the formation of a compositionally buoyant lithosphere, which may also be intrinsically more viscous by dehydration. The consequences of these melting effects on the evolution of terrestrial planets have not been explored before. The temporal evolution of crust and lithospheric mantle is modeled in a self-consistent manner considering mantle melting, convective instability, and the rewetting of dehydrated lithosphere from below by hydrogen diffusion. Though the effect of compositional buoyancy turns out to be minimal, the introduction of viscosity contrast between wet and dry mantle can considerably slow mantle cooling and sometimes lead to non-monotonic core cooling. Furthermore, with or without dehydration stiffening, our model predicts that the martian mantle must have been degassed more extensively (>80%) than previously suggested (<10%); the loss of such a large amount of water from the mantle to surface has significant implications about the role of water in the early surface and climate evolution of Mars.     

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.     

Extinct isotope heterogeneities in the mantles of Earth and Mars: Implications for mantle stirring rates

Heterogeneities in terrestrial samples for ¹⁸²W/¹⁸³W and ¹⁴²Nd/¹⁴⁴Nd are only preserved in Hadean and Archean rocks while heterogeneities in ¹²⁹Xe/¹³⁰Xe and ¹³⁶Xe/¹³⁰Xe persist to very young mantle‐derived rocks. In contrast, meteorites from Mars show that the Martian mantle preserves heterogeneities in ¹⁸²W/¹⁸³W and ¹⁴²Nd/¹⁴⁴Nd up to the present. As a consequence of the probable “deep magma ocean” core formation process, we assume that the Earth and Mars both had a very early two‐mantle‐reservoir structure with different initial extinct nuclide isotopic compositions (different ¹⁸²W/¹⁸³W, ¹⁴²Nd/¹⁴⁴Nd, ¹²⁹Xe/¹³⁰Xe, ¹³⁶Xe/¹³⁰Xe ratios). Based on this assumption, we developed a simple stochastic model to trace the evolution of a mantle with two initially distinct layers for the extinct isotopes and its development into a heterogeneous mantle by convective mixing and stretching of these two layers. Using the extinct isotope system ¹⁸²Hf‐¹⁸²W, we find that the mantles of Earth and Mars exhibit substantially different mixing or stirring rates. This is consistent with Mars having cooled faster than the Earth due to its smaller size, resulting in less efficient mantle mixing for Mars. Moreover, the mantle stirring rate obtained for Earth using ¹⁸²Hf‐¹⁸²W is consistent with the mantle stirring rate of ~500 Myr constrained by the long‐lived isotope system, ⁸⁷Rb‐⁸⁷Sr and ¹⁴⁷Sm‐¹⁴³Nd. The apparent absence of ¹⁸²W/¹⁸³W isotopic heterogeneity in modern terrestrial rocks is attributed to very active mantle stirring which reduced the ¹⁸²W/¹⁸³W isotopic heterogeneity to a relatively small scale (~83 m for a mantle stirring rate of 500 Myr) compared to the common sampling scale of terrestrial basalts (~30 or 100 km). Our results also support the “deep magma ocean” core formation model as being applicable to both Mars and Earth.     

Various aspects of the petrogenesis of the Martian shergottite meteorites

Several controversies are associated with the age and origin of the shergottite meteorites, a suite of basaltic samples from Mars. Here, it will be argued that (1) the shergottites have a young igneous age, ≤600 Myr, (2) their parent magmas were relatively dry, (3) the range of initial isotopic compositions in shergottites is most likely due to assimilation of crustal materials by mantle‐derived basaltic magmas, and (4) the intercumulus liquid compositions of shergottites such as Shergotty and Zagami are relatively well constrained.     

Crustal recycling, mantle dehydration, and the thermal evolution of Mars

We have reinvestigated the coupled thermal and crustal evolution of Mars taking new laboratory data concerning the flow behavior of iron-rich olivine into account. The low mantle viscosities associated with the relatively higher iron content of the martian mantle as well as the observed high concentrations of heat producing elements in a crust with a reduced thermal conductivity were found to promote phases of crustal recycling in many models. As crustal recycling is incompatible with an early separation of geochemical reservoirs, models were required to show no episodes of crustal recycling. Furthermore, admissible models were required to reproduce the martian crust formation history, to allow for the formation of partial melt under present day mantle conditions and to reproduce the measured concentrations of potassium and thorium on the martian surface. Taking dehydration stiffening of the mantle viscosity by the extraction of water from the mantle into account, we found that admissible models have low initial upper mantle temperatures around 1650 K, preferably a primordial crustal thickness of 30 km, and an initially wet mantle rheology. The crust formation process on Mars would then be driven by the extraction of a primordial crust after core formation, cooling the mantle to temperatures close to the peridotite solidus. According to this scenario, the second stage of global crust formation took place over a more extended period of time, waning at around 3500 Myr b.p., and was driven by heat produced by the decay of radioactive elements. Present-day volcanism would then be driven by mantle plumes originating at the core-mantle boundary under regions of locally thickened, thermally insulating crust. Water extraction from the mantle was found to be relatively efficient and close to 40% of the total inventory was lost from the mantle in most models. Assuming an initial mantle water content of 100 ppm and that 10% of the extracted water is supplied to the surface, this amount is equivalent to a 14 m thick global surface layer, suggesting that volcanic outgassing of H₂O could have significantly influenced the early martian climate and increased the planet’s habitability.     

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%.     

Implications of large elastic thicknesses for the composition and current thermal state of Mars

The martian elastic lithosphere thickness Te has recently been constrained by modeling the geodynamical response to loading at the martian polar caps and Te was found to exceed 300 km at the north pole today. Geological evidence suggests that Mars has been volcanically active in the recent past and we have reinvestigated the martian thermal evolution, identifying models which are consistent with Te>300 km and the observed recent magmatic activity. We find that although models satisfying both constraints can be constructed, special assumptions regarding the concentration and distribution of radioactive elements, the style of mantle convection and/or the mantle's volatile content need to be made. If a dry mantle rheology is assumed, strong plumes caused by, e.g., a strongly pressure dependent mantle viscosity or endothermic phase transitions near the core-mantle boundary are required to allow for decompression melting in the heads of mantle plumes. For a wet mantle, large mantle water contents of the order of 1000 ppm are required to allow for partial mantle melting. Also, for a moderate crustal enrichment of heat producing, elements the planet's bulk composition needs to be 25 and 50% sub-chondritic for dry and wet mantle rheologies, respectively. Even then, models resulting in a globally averaged elastic thicknesses of Te>300 km are difficult to reconcile with most elastic thickness estimates available for the Hesperian and Amazonian periods. It therefore seems likely that large elastic thicknesses in excess of 300 km are not representative for the bulk of the planet and that Te possibly shows a large degree of spatial heterogeneity.