Geochemistry of intermediate olivine‐phyric shergottite Northwest Africa 6234, with similarities to basaltic shergottite Northwest Africa 480 and olivine‐phyric shergottite Northwest Africa 2990

Abstract— The newly found meteorite Northwest Africa 6234 (NWA 6234) is an olivine (ol)‐phyric shergottite that is thought, based on texture and mineralogy, to be paired with Martian shergottite meteorites NWA 2990, 5960, and 6710. We report bulk‐rock major‐ and trace‐element abundances (including Li), abundances of highly siderophile elements, Re‐Os isotope systematics, oxygen isotope ratios, and the lithium isotope ratio for NWA 6234. NWA 6234 is classified as a Martian shergottite, based on its oxygen isotope ratios, bulk composition, and bulk element abundance ratios, Fe/Mn, Al/Ti, and Na/Al. The Li concentration and δ⁷Li value of NWA 6234 are similar to that of basaltic shergottites Zagami and Shergotty. The rare earth element (REE) pattern for NWA 6234 shows a depletion in the light REE (La‐Nd) compared with the heavy REE (Sm‐Lu), but not as extreme as the known “depleted” shergottites. Thus, NWA 6234 is suggested to belong to a new category of shergottite that is geochemically “intermediate” in incompatible elements. The only other basaltic or ol‐phyric shergottite with a similar “intermediate” character is the basaltic shergottite NWA 480. Rhenium‐osmium isotope systematics are consistent with this intermediate character, assuming a crystallization age of 180 Ma. We conclude that NWA 6234 represents an intermediate compositional group between enriched and depleted shergottites and offers new insights into the nature of mantle differentiation and mixing among mantle reservoirs in Mars.     

Moderately and slightly siderophile element constraints on the depth and extent of melting in early Mars

The thermal history of Mars during accretion and differentiation is important for understanding some fundamental aspects of its evolution such as crust formation, mantle geochemistry, chronology, volatile loss and interior degassing, and atmospheric development. In light of data from new Martian meteorites and exploration rovers, we have made a new estimate of Martian mantle siderophile element depletions. New high pressure and temperature metal–silicate experimental partitioning data and expressions are also available. Using these new constraints, we consider the conditions under which the Martian mantle may have equilibrated with metallic liquid. The resulting conditions that best satisfy six siderophile elements—Ni, Co, W, Mo, P, and Ga—and are consistent with the solidus and liquidus of the Martian mantle phase diagram are a pressure of 14 ± 3 GPa and temperature of 2100 ± 200 K. The Martian mantle depletions of Cr and V are also consistent with metal–silicate equilibration in this pressure and temperature range if deep mantle silicate phases are also taken into account. The results are not consistent with either metal–silicate equilibrium at the surface or at the current‐day Martian core–mantle boundary. Recent measurements and modeling have concluded that deep (～17 GPa or 1350 km) mantle melting is required to explain isotopic data for Martian meteorites and the nature of differentiation into core, mantle, and crust. This is in general agreement with our estimates of the conditions of Martian core formation based on siderophile elements that result in an intermediate depth magma ocean scenario for metal–silicate equilibrium.     

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.     

The igneous crystallization history of an ancient Martian meteorite from rare earth element microdistributions

Abstract— Rare earth element (REE) and other selected trace and minor element concentrations were measured in individual grains of orthopyroxene, feldspathic glass (of plagioclase composition) and merrillite of the ALH 84001 Martian meteorite. Unlike in other Martian meteorites, phosphate is not the main REE carrier in ALH 84001. The REE pattern of ALH 84001 bulk rock is dependent on the modal abundances of three REE-bearing phases, namely, orthopyroxene, which contains most of the heavy rare earth elements (HREEs); feldspathic glass, which dominates the Eu abundances; and merrillite, which contains the majority of the light rare earth elements (LREEs). Variations in the REE abundances previously observed in different splits of ALH 84001 can easily be explained in terms of small variations in the modal abundances of these three minerals without the need to invoke extensive redistribution of LREEs. At least some orthopyroxenes (i.e., those away from contacts with feldspathic glass) in ALH 84001 appear to have preserved their original REE zonation from igneous fractionation. An estimate of the ALH 84001 parent magma composition from that of the unaltered orthopyroxene “core” (i.e., zoned orthopyroxene with the lowest REE abundances) indicates that it is LREE depleted. This implies that the Martian mantle was already partly depleted within ～100 Ma of solar system formation, which is consistent with rapid accretion and differentiation of Mars. Although equilibration and exchange of REEs between phases (in particular, transport of LREEs into the interstitial phases, feldspathic glass and merrillite) cannot be ruled out, our data suggest that the LREE enrichment in melts “in equilibrium” with these interstitial phases is most likely the result of late-stage infiltration of the cumulate pile by a LREE-enriched melt.     

Heterogeneous distribution of H2O in the Martian interior: Implications for the abundance of H2O in depleted and enriched mantle sources

We conducted a petrologic study of apatite within 12 Martian meteorites, including 11 shergottites and one basaltic regolith breccia. These data were combined with previously published data to gain a better understanding of the abundance and distribution of volatiles in the Martian interior. Apatites in individual Martian meteorites span a wide range of compositions, indicating they did not form by equilibrium crystallization. In fact, the intrasample variation in apatite is best described by either fractional crystallization or crustal contamination with a Cl‐rich crustal component. We determined that most Martian meteorites investigated here have been affected by crustal contamination and hence cannot be used to estimate volatile abundances of the Martian mantle. Using the subset of samples that did not exhibit crustal contamination, we determined that the enriched shergottite source has 36–73 ppm H₂O and the depleted source has 14–23 ppm H₂O. This result is consistent with other observed geochemical differences between enriched and depleted shergottites and supports the idea that there are at least two geochemically distinct reservoirs in the Martian mantle. We also estimated the H₂O, Cl, and F content of the Martian crust using known crust‐mantle distributions for incompatible lithophile elements. We determined that the bulk Martian crust has ~1410 ppm H₂O, 450 ppm Cl, and 106 ppm F, and Cl and H₂O are preferentially distributed toward the Martian surface. The estimate of crustal H₂O results in a global equivalent surface layer (GEL) of ~229 m, which can account for at least some of the surface features on Mars attributed to flowing water and may be sufficient to support the past presence of a shallow sea on Mars' surface.     

Bulk chemical composition of lherzolitic shergottite Grove Mountains 99027—Constraints on the mantle of Mars

Abstract— We report the concentration of 50 elements, including rare earth elements (REEs) and platinum group elements (PGEs) in bulk samples of the Grove Mountains (GRV) 99027 lherzolitic shergottite. The abundances of REEs are distinctly lower than those of Allan Hills (ALH) A77005 and other lherzolitic shergottites, indicating that GRV 99027 is not paired with them. It may, nevertheless, sample the same igneous unit as the others (Lin et al. 2005b; Wang and Chen 2006). The CI‐normalized elemental pattern of GRV 99027 reveals low (0.004–0.008 × CI) and unfractionated PGEs (except for Pd of 0.018 × CI) without depletion of W. or Ga relative to lithophile element trends. Fractionation between siderophile and lithophile elements become less pronounced with increase of volatility, except for high abundances of Ni and Co. These characteristics are probably representative of the mantle of Mars, which is consistent with previous work that the Martian mantle formed in a deep magma ocean followed by a later accretion of chondritic materials.     

Effect of silicon on activity coefficients of Bi,Cd, Sn,and Ag in liquid Fe‐Si,and implications for differentiation and core formation

The depletion of volatile siderophile elements (VSE) Sn, Ag, Bi, Cd, and P in mantles of differentiated planetary bodies can be attributed to volatile‐depleted precursor materials (building blocks), fractionation during core formation, fractionation into and retention in sulfide minerals, and/or volatile loss associated with magmatism. Quantitative models to constrain the fractionation due to core formation have not been possible due to the lack of activity and partitioning data. Interaction parameters in Fe‐Si liquids have been measured at 1 GPa, 1600 °C and increase in the order Cd (~6), Ag (~10), Sn (~28), Bi (~46), and P (~58). These large and positive values contrast with smaller and negative values in Fe‐S liquids indicating that any chalcophile behavior exhibited by these elements will be erased by dissolution of a small amount of Si in the metallic liquid. A newly updated activity model is applied to Earth, Mars, and Vesta. Five elements (P, Zn, Sn, Cd, and In) in Earth's primitive upper mantle can largely be explained by metal‐silicate equilibrium at high PT conditions where the core‐forming metal is a Fe‐Ni‐S‐Si‐C metallic liquid, but two other—Ag and Bi—become overabundant during core formation and require a removal mechanism such as late sulfide segregation. All of the VSE in the mantle of Mars are consistent with core formation in a volatile element depleted body, and do not require any additional processes. Only P and Ag in Vesta's mantle are consistent with combined core formation and volatile‐depleted precursors, whereas the rest require accretion of chondritic or volatile‐bearing material after core formation. The concentrations of Zn, Ag, and Cd modeled for Vesta's core are similar to the concentration range measured in magmatic iron meteorites indicating that these volatile elements were already depleted in Vesta's precursor materials.     

Trace elements in mineral separates of the Peña Blanca Spring aubrite: Implications for the evolution of the aubrite parent body

Abstract— The origin of the aubrite parent body (APB) and its relation to the enstatite chondrites is still unclear. Therefore we began a detailed chemical study of the aubrite Peña Blanca Spring. Bulk samples and mineral separates (oldhamite, troilite, alabandite, pyroxene) of Peña Blanca Spring were analyzed for major and trace elements by instrumental neutron activation analysis (INAA). In addition, a leaching experiment was performed on a powdered bulk sample to study the distribution of trace elements in aubrite minerals. The elemental abundances in Peña Blanca Spring are compared to abundances in EH-chondrites and EL-chondrites in an attempt to distinguish volatility related fractionations (evaporation, condensation) from planetary differentiation (melting and core formation). Low abundances of siderophile (e.g., Ir) and chalcophile (e.g., V) elements in bulk samples indicate that 25% (by mass) metal and about 6% (by mass) sulfide separated from an enstatite chondrite like-parent body to form a core and a residual mantle with aubrite composition. We argue that the high observed rare earth element (REE) abundances in oldhamite (>100 × EH-chondrite normalized) reflect REE incorporation into oldhamite during nebular condensation. Thus, oldhamite in aubrites is, at least in part, a relict phase as originally proposed by Lodders and Palme (1990). Some re-equilibration of CaS with silicates has, however, occurred, leading to partial redistribution of REE, as exemplified by the uptake of Eu by plagioclase. The distribution of the REE among aubritic minerals cannot be the result of fractional crystallization, which would occur if high degrees of partial melting took place on the APB. Instead, the REE distributions indicate incomplete equilibrium of oldhamite and other phases. Therefore, a short non-equlibrium melting episode led to segregation of metal and sulfides.     

The composition and thickness of the crust of Mars estimated from rare earth elements and neodymium-isotopic compositions of Martian meteorites

Abstract— Isotopic and trace element compositions of Martian meteorites show that early differentiation of Mars produced complementary crustal and mantle reservoirs that were sampled by later magmatic events. This paper describes a mass balance model that estimates the rare earth element (REE) content and thickness of the crust of Mars from the compositions of shergottites. The diverse REE and Nd isotopic compositions of shergottites are most easily explained by variable addition of light rare earth element (LREE)–enriched crust to basaltic magmas derived from LREE-depleted mantle source regions. Antarctic shergottites EET 79001, ALH 77005, LEW 88516, and QUE 94201 all have strongly LREE-depleted patterns and positive initial ¹⁴³Nd isotopic compositions, which is consistent with the generation of these magmas from depleted mantle sources and little or no interaction with enriched crust. In contrast, Shergotty and Zagami have negative initial ¹⁴³Nd isotopic compositions and less pronounced depletions of the LREE, which have been explained by incorporation of enriched crustal components into mantle-derived magmas (Jones, 1989; Longhi, 1991; Borg et al., 1997). The mass balance model presented here derives the REE composition of the crustal component in Shergotty by assuming it represents a mixture between a mantle-derived magma similar in composition to EET 79001A and a LREE-enriched crustal component. The amount of crust in Shergotty is constrained by mixing relations based on Nd-isotopic compositions, which allows the REE pattern of the crustal component to be calculated by mass balance. The effectiveness of this model is demonstrated by the successful recovery of important characteristics of the Earth's continental crust from terrestrial Columbia River basalts. Self-consistent results for Nd-isotopic compositions and REE abundances are obtained if Shergotty contains ～10–30% of LREE-enriched crust with >10 ppm Nd. This crustal component would have moderately enriched LREE (Sm/Nd = 0.25–0.27; ¹⁴⁷Sm/¹⁴⁴Nd = 0.15–0.17; La/Yb = 2.7–3.8), relatively unfractionated heavy rare earth elements (HREE), and no Eu anomaly. Crust with these characteristics can be produced from a primitive lherzolitic Martian mantle by modest amounts (2–8%) of partial melting, and it would have a globally averaged thickness of <45 km, which is consistent with geophysical estimates. Mars may serve as a laboratory to investigate planetary differentiation by extraction of a primary basaltic crust.     

Characterization of weathering and heterogeneous mineral phase distribution in brachinite Northwest Africa 4872

Terrestrial weathering of hot desert achondrite meteorite finds and heterogeneous phase distributions in meteorites can complicate interpretation of petrological and geochemical information regarding parent‐body processes. For example, understanding the effects of weathering is important for establishing chalcophile and siderophile element distributions within sulfide and metal phases in meteorites. Heterogeneous mineral phase distribution in relatively coarsely grained meteorites can also lead to uncertainties relating to compositional representativeness. Here, we investigate the weathering and high‐density (e.g., sulfide, spinel, Fe‐oxide) phase distribution in sections of ultramafic achondrite meteorite Northwest Africa (NWA) 4872. NWA 4872 is an olivine‐rich brachinite (Fo_{63.6 ± 0.5}) with subsidiary pyroxene (Fs_9.7 ± 0.1Wo_{46.3 ± 0.2}), Cr‐spinel (Cr# = 70.3 ± 1.1), and weathered sulfide and metal. Raman mapping confirms that weathering has redistributed sulfur from primary troilite, resulting in the formation of Fe‐oxide (‐hydroxide) and marcasite (FeS₂). From Raman mapping, NWA 4872 is composed of olivine (89%), Ca‐rich pyroxene (0.4%), and Cr‐spinel (1.1%), with approximately 7% oxidized metal and sulfide and 2.3% marcasite‐dominated sulfide. Microcomputed tomography (micro‐CT) observations reveal high‐density regions, demonstrating heterogeneities in mineral distribution. Precision cutting of the largest high‐density region revealed a single 2 mm Cr‐spinel grain. Despite the weathering in NWA 4872, rare earth element (REE) abundances of pyroxene determined by laser‐ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) indicate negligible modification of these elements in this mineral phase. The REE abundances of mineral grains in NWA 4872 are consistent with formation of the meteorite as the residuum of the partial melting process that occurred on its parent body. LA‐ICP‐MS analyses of sulfide and alteration products demonstrate the mobility of Re and/or Os; however, highly siderophile element (HSE) abundance patterns remain faithful recorders of processes acting on the brachinite parent body(ies). Detailed study of weathering and phase distribution offers a powerful tool for assessing the effects of low‐temperature alteration and for identifying robust evidence for parent‐body processes.     

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.     

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.     

Martian meteorites: Volatile trace elements and cluster analysis

Abstract— We report data for 15 mainly volatile trace elements (Ag, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Sb, Se, Te, Tl, U, Zn) by radiochemical neutron activation analysis (RNAA) in whole-rock samples of five Martian meteorites that, with seven others studied earlier, complete the 12 member Martian meteorite suite. Nearly all of these elements exhibit highly variable compositional continua and are richer in the Martian suite compared with other basaltic meteorites. From cluster analysis, we find that the clustering of subtypes based on these elements is virtually identical to that based on contents of major refractory elements and mineralogic/petrographic character istics, which implies that each source region on Mars was closed to volatile transport. Martian meteorite data can be used to infer volatile element contents in that planet.     

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%.     

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.     

Accretion in the inner nebula: The relationship between terrestrial planetary compositions and meteorites*

Abstract— The bulk compositions of the terrestrial planets are assessed. Venus and Earth probably have similar bulk compositions, but Mars is enriched in volatile elements. The inner planets are all depleted in volatile elements, as shown by K/U ratios, relative to most meteorites and the CI primordial values. Terrestrial upper mantle Mg/Si ratios are high compared with CI data. If they are representative of the bulk Earth, then the Earth accreted from a segregated suite of planetesimals that had non-chondritic major element abundances. The CI meteorite abundances, despite aqueous alteration, match the solar data and provide the best estimate for the composition of the solar nebula, including the iron abundance. The widespread depletion of volatile elements in the inner solar nebula is most likely caused by heating related to early violent solar activity (e.g., T Tauri and FU Orionis stages) which, for example, drove water out to a “snow line” in the vicinity of Jupiter. The variation in composition among the meteorites and the apparent lack of mixing among the groups indicates accretion from narrow feeding zones. There appears to have been little mixing between meteorite and planetary formation zones, as shown by the oxygen isotope variations, lack of mixing of meteorite groups, and differences in K/U ratios. In summary, it appears that the final accretion of planets did not result in widespread homogenization, and that mixing zones were not more than about 0.3 A.U. wide. Although the composition of the Moon is unique, and its origin due to an essentially random event, its presence reinforces the planetesimal hypothesis and the importance of stochastic processes during planetary accretion in the inner solar system.     

Detailed abundances of rare earth elements,thorium and uranium in chondritic meteorites: An ICP-MS study

Abstract— Inductively coupled plasma mass spectrometry (ICP-MS) was successfully applied to bulk samples of Allende, Jilin, Modoc, Saint-Séverin and Atlanta for the determination of rare earth elements (REE) (Y and 14 lanthanoids), Th and U. The results of ICP-MS showed good agreement with recommended values, and their reproducibilities were high enough to discuss the detailed abundances of lanthanoids and actinoids in chondritic meteorites. For the Allende reference sample issued by the Smithsonian Institution, a positive anomaly of Tm, a fractionation between light REE and heavy REE and a high Th/U ratio were observed in the CI-normalized abundances of REE, Th and U. These features are common for group II inclusions in Allende, suggesting that the abundances of refractory lithophiles in Allende are somewhat influenced by those in a specific constituent. For the other chondritic meteorites, a zigzag alteration was commonly observed in the heavy-REE region of their CI-normalized abundance patterns. It is suggested that such a zigzag pattern is attributable to erratically high abundances of monoisotopic REE (Tb, Ho and Tm) in the CI values. Abundances of REE, Th and U in the bulk samples are also discussed separately in detail.     

Geochemical diversity of shergottite basalts: Mixing and fractionation,and their relation to Mars surface basalts

The chemical compositions of shergottite meteorites, basaltic rocks from Mars, provide a broad view of the origins and differentiation of these Martian magmas. The shergottite basalts are subdivided based on their Al contents: high‐Al basalts (Al > 5% wt) are distinct from low‐Al basalts and olivine‐phyric basalts (both with Al < 4.5% wt). Abundance ratios of highly incompatible elements (e.g., Th, La) are comparable in all the shergottites. Abundances of less incompatible elements (e.g., Ti, Lu, Hf) in olivine‐phyric and low‐Al basalts correlate well with each other, but the element abundance ratios are not constant; this suggests mixing between components, both depleted and enriched. High‐Al shergottites deviate from these trends consistent with silicate mineral fractionation. The “depleted” component is similar to the Yamato‐980459 magma; approximately, 67% crystal fractionation of this magma would yield a melt with trace element abundances like QUE 94201. The “enriched” component is like the parent magma for NWA 1068; approximately, 30% crystal fractionation from it would yield a melt with trace element abundances like the Los Angeles shergottite. This component mixing is consistent with radiogenic isotope and oxygen fugacity data. These mixing relations are consistent with the compositions of many of the Gusev crater basalts analyzed on Mars by the Spirit rover (although with only a few elements to compare). Other Mars basalts fall off the mixing relations (e.g., Wishstone at Gusev, Gale crater rocks). Their compositions imply that basalt source areas in Mars include significant complexities that are not present in the source areas for the shergottite basalts.     

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.