Basaltic magmatism and the bulk composition of the moon

The lunar interior is comprised of two major petrological provinces: (1) an outer zone several hundred km thick which experienced partial melting and crystallization differentiation 4.4–4.6 b.y. ago to form the lunar crust together with an underlying complementary zone of ultramafic cumulates and residua, and (2) the primordial deep interior which was the source region for mare basalts (3.2–3.8 b.y.) and had previously been contaminated to varying degrees with highly fractionated material derived from the 4.4–4.6 b.y. differentiation event. In both major petrologic provinces, basaltic magmas have been produced by partial melting. The chemical characteristics and high-pressure phase relationships of these magmas can be used to constrain the bulk compositions of their respective source regions.Primitive low-Ti mare basalts (e.g., 12009, 12002, 15555 and Green Glass) possessing high normative olivine and high Mg and Cr contents, provide the most direct evidence upon the composition of the primordial deep lunar interior. This composition, as estimated on the basis of high pressure equilibria displayed by the above basalts, combined with other geochemical criteria, is found to consist of orthopyroxene + clinopyroxene + olivine with total pyroxenes > olivine, 100 MgO/(MgO + FeO) = 75–80, about 4% of CaO and Al₂O₃ and 2× chondritic abundances of REE, U and Th. This composition is similar to that of the earth's mantle except for a higher pyroxene/olivine ratio and lower 100 MgO/(MgO + FeO).The lunar crust is believed to have formed by plagioclase elutriation within a vast ocean of parental basaltic magma. The composition of the latter is found experimentally by removing liquidus plagioclase from the observed mean upper crust (gabbroic anorthosite) composition, until the resulting composition becomes multiply saturated with plagioclase and a ferromagnesian phase (olivine). This parental basaltic composition is almost identical with terrestrial oceanic tholeiites, except for partial depletion in the two most volatile components, Na₂ and SiO₂. Similarity between these two most abundant classes of lunar and terrestrial basaltic magmas strongly implies corresponding similarities between their source regions. The bulk composition of the outer 400 km of the Moon as constrained by the 4.6-4.4 b.y. parental basaltic magma is found to be peridotitic, with olivine > pyroxene, 100 MgO/ (MgO + FeO) 86, and about 2× chondritic abundances of Ca, Al and REE. The Moon thus appears to have a zoned structure, with the deep interior (below 400 km) possessing somewhat higher contents of FeO and SiO₂ than the outer 400 km. This zoned model, derived exclusively on petrological grounds, provides a quantitative explanation of the Moon's mean density, moment of inertia and seismic velocity profile.The bulk composition of the entire Moon, thus obtained, is very similar to the pyrolite model composition for the Earth's mantle, except that the Moon is depleted in Na (and other volatile elements) and somewhat enriched in iron. The similarity in major element composition extends also to the abundances of REE, U and Th. These compositional similarities, combined with the identity in oxygen isotope ratios between the Moon and the Earth's mantle, are strongly suggestive of a common genetic relationship.     

Procrustean science: Indigenous siderophiles in the lunar highlands,according to Delano and Ringwood

The best estimate of indigenous lunar siderophiles comes from 29 pristine lunar rocks, characterized by low siderophile abundances, plutonic textures, and high age. Delano and Ringwood's blanket rejection of these rocks, on the contention that they are impact melts, is not justified by the petrologic evidence. Contrary to their claims, gold in highland breccias is largely meteoritic and is unaffected by fumarolic volcanism, as shown by its correlation with Ir and noncorrelation with fumarolic T1 (r=0.896 and 0.272). Delano and Ringwood's approach, involving subtraction of an H-chondrite meteoritic component from highland breccias, ignores the variation of Ir/Au ratios in modern and ancient meteorites, and hence leads to spurious excesses of Au, Ni, and volatiles, and in some cases to physically meaningless, negative residuals. Their excess volatiles in highland crust relative to mare basalts disappear when the highland composition is based on pristine lunar rocks rather than under-corrected breccias. Contrary to claims by Delano and Ringwood, the Ni/Co trend in Apollo 16 samples cannot be explained by an indigenous component rich in Ni (150–200 ppm) and Co (30–45ppm); mixing lines show that much lower Ni and Co contents are required (e.g., 7 ppm each).Chondrites and lunar highland breccias show essentially parallel fractionation trends for the siderophile-element ratios Re/Ir, Au/Ir, Ni/Ir, Ni/Pd, and Os/Ir. Because the chondritic ratios were established in the solar nebula, it appears that the lunar ratios also reflect nebular processes, and have not been modified by planetary processes.Properly derived abundances for the lunar highlands show large, systematic depletions relative to terrestrial oceanic tholeiites, by the following factors: Ge 270, Re 230, Sb170, Zn150, Au60, Tl 50, Ag 48, Ni 42, Se 12. It would seem that the resemblance to the Earth's mantle is not quite as striking as claimed by Delano and Ringwood.     

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.     

Compositional evidence regarding the influx of interplanetary materials onto the lunar surface

Siderophilic element/Ir ratios are higher in mature lunar soils from highlands sites than in those from mare sites. We infer that the population of materials responsible for the early intense bombardment of the Moon had high ratios, and that the population responsible for the essentially constant flux has low ratios. No group of chondrites has siderophile/Ir ratios identical to those in the mare or highlands soils; CM chondrites are the most similar, and CM-like materials may account for a major fraction of Earth-crossing materials during the past 3.7 b.y.Siderophile/Ir ratios may be used to determine the amount of highlands regolith in soils or breccias from the mare-highlands interface areas (Apollo 15 and 17), and to infer the time of formation of highlands breccias whose sideropbiles originated in mature soils. Arguments are summarized against the viewpoint that the siderophiles in most highlands breccias originated in basin-forming projectiles. Differences in mature soil siderophile concentrations at Apollo 14 and 16 indicate a substantially greater concentration at the latter site immediately following the Imbrium event.Siderophile concentrations are used to estimate mean regolith depths at the landing sites; as relative values these are more precise than estimates based on seismic or crater observations. The longlived flux is calculated to be 2.9 g cm^–2 b.y.^–1 averaged over the past 3.7 b.y. A consideration of the relationship between mass fluence and time indicates that the mass flux decreased with a half-life of about 40 m.y. immediately following the Imbrium event.     

Tungsten isotopes in ferroan anorthosites: Implications for the age of the Moon and lifetime of its magma ocean

New W isotope data for ferroan anorthosites 60025 and 62255 and low-Ti mare basalt 15555 show that these samples, contrary to previous reports [Lee, D.C., et al., 1997. Science 278, 1098-1103; Lee, D.C., et al., 2002. Earth Planet. Sci. Lett. 198, 267-274], have a W isotope composition that is indistinguishable from KREEP and other mare basalts. This requires crust extraction on the Moon later than ∼60 Myr after CAI formation, consistent with ¹⁴⁷Sm-¹⁴³Nd ages for ferroan anorthosites. The absence of ¹⁸²Hf-induced ¹⁸²W variations in the Moon is consistent with formation of the Moon at after CAI formation that has been inferred based on the indistinguishable ¹⁸²W/¹⁸⁴W ratios of the bulk Moon and the bulk silicate Earth. The uncertainties on the age of the Moon and the age of the oldest lunar samples currently hamper a precise determination of the duration of magma ocean solidification and are consistent with both an almost immediate crystallization and a more protracted timescale of ∼100 Myr.     

Siderophile and chalcophile element abundances in shergottites: Implications for Martian core formation

Elemental abundances for volatile siderophile and chalcophile elements for Mars inform us about processes of accretion and core formation. Such data are few for Martian meteorites, and are often lacking in the growing number of desert finds. In this study, we employed laser ablation inductively coupled plasma–mass spectrometry (LA‐ICP‐MS) to analyze polished slabs of 15 Martian meteorites for the abundances of about 70 elements. This technique has high sensitivity, excellent precision, and is generally accurate as determined by comparisons of elements for which literature abundances are known. However, in some meteorites, the analyzed surface is not representative of the bulk composition due to the over‐ or underrepresentation of a key host mineral, e.g., phosphate for rare earth elements (REE). For other meteorites, the range of variation in bulk rastered analyses of REE is within the range of variation reported among bulk REE analyses in the literature. An unexpected benefit has been the determination of the abundances of Ir and Os with a precision and accuracy comparable to the isotope dilution technique. Overall, the speed and small sample consumption afforded by this technique makes it an important tool widely applicable to small or rare meteorites for which a polished sample was prepared. The new volatile siderophile and chalcophile element abundances have been employed to determine Ge and Sb abundances, and revise Zn, As, and Bi abundances for the Martian mantle. The new estimates of Martian mantle composition support core formation at intermediate pressures (14 ± 3 GPa) in a magma ocean on Mars.     

Petrography,mineralogy, and geochemistry of lunar meteorite Sayh al Uhaymir 300

Abstract— We report here the petrography, mineralogy, and geochemistry of lunar meteorite Sayh al Uhaymir 300 (SaU 300). SaU 300 is dominated by a fine‐grained crystalline matrix surrounding mineral fragments (plagioclase, pyroxene, olivine, and ilmenite) and lithic clasts (mainly feldspathic to noritic). Mare basalt and KREEPy rocks are absent. Glass melt veins and impact melts are present, indicating that the rock has been subjected to a second impact event. FeNi metal and troilite grains were observed in the matrix. Major element concentrations of SaU 300 (Al₂O₃ 21.6 wt% and FeO 8.16 wt%) are very similar to those of two basalt‐bearing feldspathic regolith breccias: Calcalong Creek and Yamato (Y‐) 983885. However, the rare earth element (REE) abundances and pattern of SaU 300 resemble the patterns of feldspathic highlands meteorites (e.g., Queen Alexandra Range (QUE) 93069 and Dar al Gani (DaG) 400), and the average lunar highlands crust. It has a relatively LREE‐enriched (7 to 10 x CI) pattern with a positive Eu anomaly (?11 x CI). Values of Fe/Mn ratios of olivine, pyroxene, and the bulk sample are essentially consistent with a lunar origin. SaU 300 also contains high siderophile abundances with a chondritic Ni/Ir ratio. SaU 300 has experienced moderate terrestrial weathering as its bulk Sr concentration is elevated compared to other lunar meteorites and Apollo and Luna samples. Mineral chemistry and trace element abundances of SaU 300 fall within the ranges of lunar feldspathic meteorites and FAN rocks. SaU 300 is a feldspathic impact‐melt breccia predominantly composed of feldspathic highlands rocks with a small amount of mafic component. With a bulk Mg# of 0.67, it is the most mafic of the feldspathic meteorites and represents a lunar surface composition distinct from any other known lunar meteorites. On the basis of its low Th concentration (0.46 ppm) and its lack of KREEPy and mare basaltic components, the source region of SaU 300 could have been within a highland terrain, a great distance from the Imbrium impact basin, probably on the far side of the Moon.     

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.     

Does the Moon Have a Metallic Core?: Constraints from Giant Impact Modeling and Siderophile Elements

The issue of whether the Moon has a small metallic core is reexamined in light of new information: improved dynamical modeling, new constraints on core size, and high temperature and pressure metal-silicate partition coefficients. Addressed specifically is the question of whether the Moon's siderophile element budget can be explained by derivation of the Moon from a differentiated impactor or proto-Earth (stage 1), followed by formation of a small metallic core within the Moon (stage 2). If the Moon is made of mantle material from either a “hot” impactor or a “warm” impactor or proto-Earth, a small metallic core (0.7 to 2 mass%) is predicted. If the Moon is made from mantle material from a “hot” proto-Earth, the lunar mantle would be more depleted in W or Re than is observed. Scenarios in which the Moon is made from impactor or proto-Earth mantle material that has equilibrated with metal at low pressures and temperatures (“cold” scenarios) would yield a much larger metallic core than observed. Finally, the greater depletions of Ni, Mo, and Re in the Moon (relative to the Earth) can be explained by low PT and reduced metal-silicate equilibrium in an impactor without later core formation in the Moon (i.e., no stage 2), but depletions of Co, Ga, and W cannot. Altogether, geochemically unlikely or geophysically inadequate non-metallic core alternatives, substantial geophysical evidence for a metallic core, and the successful models presented here for siderophile element depletions all favor the presence of a small lunar metallic core. Previous geochemical objections to an impactor origin of the Moon are eliminated because siderophile element concentrations in the lunar mantle are consistent with separation of a small core from a bulk Moon derived from impactor mantle material.     

Petrogenesis of Chang'E-5 young mare low-Ti basalts

The regolith samples returned by the Chang'E-5 mission (CE-5) contain the youngest radiometrically dated mare basaltic clasts, which provide an opportunity to elucidate the magmatic activities on the Moon during the late Eratosthenian. In this study, detailed petrographic observations and comprehensive geochemical analyses were performed on the CE-5 basaltic clasts. The major element concentrations in individual plagioclase grain of the CE-5 basalts may vary slightly from core to rim, whereas pyroxene has clear chemical zonation. The crystallization sequence of the CE-5 mare basalts was determined using petrographic and geochemical relations in the basaltic clasts. In addition, both fractional crystallization (FC) and assimilation and fractional crystallization models were applied to simulate the chemical evolution of melt equilibrated with plagioclase in CE-5 basalts. Our results reveal that the melt had a TiO₂ content of ~3 wt% and an Mg# of ~45 at the onset of plagioclase crystallization, suggesting a low-Ti parental melt of the CE-5 basalts. The relatively high FeO content (>14.5 wt%) in melt equilibrated with plagioclase could have resulted in extensive crystallization of ilmenite, unlike in Apollo low-Ti basalts. Furthermore, our calculations showed that the geochemical evolution of CE-5 basaltic melt could not have occurred in a closed system. On the contrary, the CE-5 basalts could have assimilated mineral, rock, and glass fragments that have higher concentrations of KREEP elements (potassium, rare earth elements, and phosphorus) in the regolith during magma flow on the Moon's surface. The presence of the KREEP signature in the CE-5 basalts is consistent with literature remote sensing data obtained from the CE-5 landing site. These KREEP-bearing fragments could originate from KREEP basaltic melts that may have been emplaced at the landing site earlier than the CE-5 basalts.     

The lunar geochemistry of chromium and vanadium

Crystal/liquid partition coefficients for Cr, V, Mn, and Fe have been determined experimentally between olivine, orthopyroxene, clinopyroxene and silicate melt possesing the composition of a primitive lunar green glass, at oxygen fugacities appropriate to the lunar interior. These species all behave essentially as compatible elements and possess crystal/liquid partition coefficients mostly between 0.3 and 0.9. Partition coefficients for Cr, V, and Mn are generally similar to those of Fe. This implies that crystal/liquid fractionation processes in the lunar interior which do not involve the participation of spinels would not have been effective in fractionating MnO, CrO, and VO from FeO. The well-known constancy of FeO/MnO ratios in nearly all lunar rocks is a reflection of this behaviour. It is shown that comparably strong correlations between CrO-;FeO and VO-;FeO exist for lunar highland breccias and soils from all sites and that these correlations extend to primitive lunar volcanic glasses associated with mare volcanism, strongly suggesting that the CrO/FeO and VO/FeO ratios so derived are of global importance. The observed ratios characterizing differentiated regions of the Moon can be combined with the corresponding ratios for residual refractory portions of the Moon, using measured partition coefficients for Fe, Mg, Cr, V, and Mn between olivine, orthopyroxene and liquid. Bulk Moon abundances for Cr and V have been calculated for a range of reasonable assumptions concerning the petrogenetic relationships between differentiated portions of the Moon and complementary refractory residua consisting of olivine and orthopyroxene mineralogies. Because of the small differences in crystal liquid partition coefficients between FeO, CrO, and VO, these estimates are insensitive to large variations in the models. The bulk Moon is accordingly estimated to contain 2190–2463 ppm Cr and 79–95 ppm V. These values are very similar to the Cr and V contents of the Earth's mantle, estimated as 3010 ppm Cr and 81 ppm V by Sun (1982). The geochemical implications of these similarities are discussed.     

Some aspects of the minor element chemistry of lunar mare basalts

The principal minor element (including Ti) characteristics of mare basalts which must be explained by an acceptable theory of petrogenesis are reviewed. Thes include: (i) Theabsolute abundances of incompatible elements vary over a twentyfold range yet therelative abundances within this group rarely deviate by more than a factor of two from the chondritic relative abundances. (ii) The sizes of the europium and strontium anomalies show a general trend to decrease as the absolute abundances of incompatible elements decrease. This trend is also one of increasing degree of partial melting and implies that the source region did not possess intrinsic Eu or Sr anomalies. (iii) Titanium seems to behave largely as an incompatible element. (iv) Many mare basalts have Rb/Sr model ages of about 4.5 b.y. whereas their crystallization ages are 3.2–3.8 b.y.Recent hypotheses have proposed that mare basalts formed by equilibrium partial melting of pyroxene-rich cumulates which underlay and were complementary to the anorthositic crust. According to a variant of this category, the residual liquid resulting from fractional crystallization of the highlands and their complementary cumulates segregated to form an intermediate layer between the highlands and the underlying primary cumulates. This highly fractionated residual liquid crystallized to form a pyroxene-olivine-ilmenite assemblage. High-Ti mare basalts subsequently formed by partial melting of this layer, whereas low-Ti basalts formed by partial melting of the underlying cumulates. These hypotheses are examined in detail and are rejected on several grounds.A new hypothesis based upon partial melting under conditions of surface or local equilibrium is proposed. It is assumed that the moon accreted from material which had ultimately formed by fractional condensation from a gas phase of appropriate composition. The essential members of the condensation sequence with falling temperature were perovskite, melilite, spinel, fassaite, forsterite, enstatite, alkali felspar. As the gas cooled over an extended period (>100 yr) large megacrysts (> 1 m) were formed. Trace elements were partitioned into these phases according to equilibrium condensation and crystal chemical relationships. Trivalent rare earths and other incompatible elements mainly entered perovskite, most of the Eu and Sr entered melilite whilst Rb entered alkali felspar. Radiogenic⁸⁷Sr thus produced remained within the alkali felspar. The moon accreted from a mixture of these condensates to form a disequilibrium mineral assemblagewith a bulk composition similar to that of the pyroxenite source region of mare basalts as derived from experimental petrological considerations. After heating deep in the lunar interior, solid state reaction occurred around megacryst boundaries to form an equilibrium pyroxenite containing large unreacted cores of refractory melilite and perovskite. The latter mineral readily forms low melting point liquids when in contact with pyroxenes whereas melilite remains relatively inert. As partial melting commenced, all the perovskite and other low-melting accessory minerals (eg. alk. felspar) entered the first batch of liquid which thereby received most of the incompatible elements and⁸⁷Sr (but not Eu and common Sr) present in the source region. Further melting of the pyroxenite matrix occurred under conditions of surface equilibrium. As the degree of partial melting increased, the first batch of incompatible-element-rich liquid was diluted by major elements from the pyroxenite matrix whilst refractory melilite cores were gradually consumed, thereby supplying relatively constant amounts of Eu and Sr to liquids so produced. It is considered that this model is capable of explaining the principal minor element characteristics of mare basalts and is consistent with interpretations of the major element chemistry of their source region based upon experimental petrology.     

Geochemistry of diogenites: Still more diversity in their parental melts

Abstract— We report on the major and trace element abundances of 18 diogenites, and O‐isotopes for 3 of them. Our analyses extend significantly the diogenite compositional range, both in respect of Mg‐rich (e.g., Meteorite Hills [MET] 00425, MgO = 31.5 wt%) and Mg‐poor varieties (e.g., Dhofar 700, MgO = 23 wt%). The wide ranges of siderophile and chalcophile element abundances are well explained by the presence of inhomogeneously distributed sulfide or metal grains within the analyzed chips. The behavior of incompatible elements in diogenites is more complex, as exemplified by the diversity of their REE patterns. Apart from a few diogenite samples that contain minute amounts of phosphate, and whose incompatible element abundances are unlike the orthopyroxene ones, the range of incompatible element abundances, and particularly the range of Dy/Yb ratios in diogenites is best explained by the diversity of their parental melts. We estimate that the FeO/MgO ratios of the diogenite parental melts range from about 1.4 to 3.5 and therefore largely overlap the values obtained for non‐cumulate eucrites. Our results rule out the often accepted view that all the diogenites formed from parental melts more primitive than eucrites during the crystallization of a magma ocean. Instead, they point to a more complex history, and suggest that diogenites were derived from liquids produced by the remelting of cumulates formed from the magma ocean.     

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.     

Magnesian anorthositic granulites in lunar meteorites Allan Hills A81005 and Dhofar 309: Geochemistry and global significance

Abstract– Fragments of magnesian anorthositic granulite are found in the lunar highlands meteorites Allan Hills (ALH) A81005 and Dhofar (Dho) 309. Five analyzed clasts of meteoritic magnesian anorthositic granulite have Mg′ [molar Mg/(Mg + Fe)] = 81–87; FeO ≈ 5% wt; Al₂O₃ ≈ 22% wt; rare earth elements abundances ≈ 0.5–2 × CI (except Eu ≈ 10 × CI); and low Ni and Co in a non‐chondritic ratio. The clasts have nearly identical chemical compositions, even though their host meteorites formed at different places on the Moon. These magnesian anorthositic granulites are distinct from other highlands materials in their unique combination of mineral proportions, Mg′, REE abundances and patterns, Ti/Sm ratio, and Sc/Sm ratio. Their Mg′ is too high for a close relationship to ferroan anorthosites, or to have formed as flotation cumulates from the lunar magma ocean. Compositions of these magnesian anorthositic granulites cannot be modeled as mixtures of, or fractionates from, known lunar rocks. However, compositions of lunar highlands meteorites can be represented as mixtures of magnesian anorthositic granulite, ferroan anorthosite, mare basalt, and KREEP. Meteoritic magnesian anorthositic granulite is a good candidate for the magnesian highlands component inferred from Apollo highland impactites: magnesian, feldspathic, and REE‐poor. Bulk compositions of meteorite magnesian anorthositic granulites are comparable to those inferred for parts of the lunar farside (the Feldspathic Highlands Terrane): ～4.5 wt% FeO; ～28 wt% Al₂O₃; and Th <1 ppm. Thus, magnesian anorthositic granulite may be a widespread and abundant component of the lunar highlands.     

Lunar meteorite Queen Alexandra Range 93069 and the iron concentration of the lunar highlands surface

Abstract— Lunar meteorite Queen Alexandra Range 93069 is a clast-rich, glassy-matrix regolith breccia of ferroan, highly aluminous bulk composition. It is similar in composition to other feldspathic lunar meteorites but differs in having higher concentrations of siderophile elements and incompatible trace elements. Based on electron microprobe analyses of the fusion crust, glassy matrix, and clasts, and instrumental neutron activation analysis of breccia fragments, QUE 93069 is dominated by nonmare components of ferroan, noriticanorthosite bulk composition. Thin section QUE 93069,31 also contains a large, impact-melted, partially devitrified clast of magnesian, anorthositic-norite composition. The enrichment in Fe, Sc, and Cr and lower Mg/Fe ratio of lunar meteorites Yamato 791197 and Yamato 82192/3 compared to other feldspathic lunar meteorites can be attributed to a small proportion (5–10%) of low-Ti mare basalt. It is likely that the nonmare components of Yamato 82192/3 are similar to and occur in similar abundance to those of Yamato 86032, with which it is paired. There is a significant difference between the average FeO concentration of the lunar highlands surface as inferred from the feldspathic lunar meteorites (mean: ～5.0%; range: 4.3–6.1%) and a recent estimate based on data from the Clementine mission (3.6%).     

On the origin of the moon by rotational fission

Based on simple CIPW norms for the proposed terrestrial upper mantle material, it is shown that if the Moon fissioned from the Earth and gravitationally differentiated, it could have a 72 km thick anorthosite (An₉₇) crust, a calcium poor (3.8% by weight) pyroxenite upper mantle 100 Mg/Mg + Fe = 75 to 80) ending at a depth of 313 km and a dunite (Fo_{93_95}) lower mantle below a depth of 313 km. Refinements of these simple norm models, based on the cooling history, crystallization sequence and the variations of the 100 Mg/Mg + Fe ratio of the liquid and crystals during the crystallization sequence, indicate that the final form of such a Moon could have the following properties: (1) a primitive, cumulate anorthosite - minor troctolite crust with intrusive and extrusive feldspathic basalts and KREEP rich norites; the thickness of this crust would be 75 km; (2) a zone in the bottom of the crust and the top of the upper mantle which is rich in KREEP, the incompatible elements, silica, and possibly voltiles; this zone would be the source area for the upland feldspathic basalts, KREEP rich norites and KREEP and silica rich fluids; (3) an upper mantle between the depths of 75 km and 350 to 400 km which consists of peridotite containing 80–85% pyroxene (Wo₁₀En_{68_72}Fs_{18_22}) and 15–20% olivine (Fo_{75_80}); the Al₂O₃ content of the upper mantle is 3%; the peridotite layer would be the source area for mare basalts and; (4) a lower mantle below a depth of 350–400 km which consists of dunite (Fo_{93_97}).The cooling history of such a moon indicates that the primitive anorthosite crust would have been completely formed within 10⁸ yr after fission. The extrusion and intrusion of upland basalts and KREEP rich norites and the metamorphism of the crustal rocks via KREEP and silica rich fluids would have ended about 4 × 10⁹ yr ago when cooling well below the solidus reached a depth of 150 km. As cooling continied, the only source of magmas after 4 × 10⁹ yr ago would have been the peridotite upper mantle, i.e. the source area of the mare basalts. Extrusion of mare basalts ended when cooling below the solidus reached the top of the refractory dunite lower mantle 3-3.3 × 10⁹ yr ago.Thus, it is shown that the chemistry, primary lithology, structure and developmental history of a fissioned Moon readily match those known for the real Moon. As such, the models presented in this paper strongly support the fission origin of the Moon.Guest Scientist, supported by the Alexander von Humboldt-Stiftung.Permanent Address.     

On the petrology and structure of a gravitionally differentiated moon of fission origin

In a previous paper, it was shown that the basic properties and the developmental history of a gravitationally differentiated Moon of fission origin match those known for the Moon. In the first part of this report, the models of a differentiated Moon are critically reviewed based on second order considerations of some of the chemical systems used to develope the earlier models and based on new lunar data. As a result, slightly updated models are developed and the results indicate that a Moon of fission origin has a feldspar rich crust (≈70% Or_0.8Ab_5.3An_93.9 with ≈30% pyroxene and olivine) reaching an average depth of ≈65 km. A KREEP rich layer is located at the interface of the crust and the upper mantle. The upper mantle consists of peridotite (≈80% Wo₁₀En₇₀Fs₂₀ and ≈20% Fo_75–80 with ≈3% Al₂O₃ and ≈ 2% TiO₂) and reaches a depth of 300–400 km. Below 300–400 km lies a dunite (≈Fo₉₅) lower mantle. A simple model for the distribution of K, U and Th (and by inference, KREEP) in the differentiated Moon model is developed using a distribution coefficient of 0.1 for the three elements. This coefficient is derived from published data on the distribution of U in Apollo 11 basalts. The simple model successfully accounts for the observed K, U and Th contents of the various mare basalts and upland rocks and yields a heat flow of 21 erg cm^?2s^?1 for the Moon. A model for the fine structure of the peridotite upper mantle of the model Moon is developed based on the TiO₂ and trace element variations observed in the various mare basalts. It is proposed that the upper mantle is rhythmically banded on the scale of 10's of km and that this banding leads to local variations of a factor of ±3 in the K, U and Th content, _-10 ⁺⁵ in the TiO₂ content and _-∞ ⁺² in the olivine content of the peridotite. It is also proposed that this banding leads to large scale horizontal inhomogenuities in the composition of the upper mantle. It is also shown that the formation of the primitive suite of upland rocks is easily explained by the cumulation of plagioclase, which carried varying amounts of pyroxene, olivine and melt with it, during the peritectic crystallization of the last 20% of the differentiating Moon. It is found that the 100 Mg/(Mg+Fe) ratios of the mafics and the An contents of the plagioclases of the rocks are controlled by several factors, the most important of which is the ratio of melt to crystals which together formed the various upland rocks. The inverse relationship between the An contents and the Mg contents of the upland rocks is a direct consequence of the differentiation sequence proposed. The results and models presented in this paper further support the hypothesis that the Moon formed as a result of fission from the proto-Earth.     

Electrical conductivity anomaly beneath mare serenitatis detected by Lunokhod 2 and Apollo 16 magnetometers

Magnetic fluctuations measured by the Lunokhod 2 magnetometer in the Bay Le Monnier are distinctly anisotropic when compared to simultaneous Apollo 16 magnetometer data measured 1100 km away in the Descartes highlands. This anisotropy can be explained by an anomalous electrical conductivity of the upper mantle beneath Mare Serenitatis. A model is presented of anomalously lower electrical conductivity beneath Serenitatis and the simultaneous magnetic data from the Lunokhod 2 site at the mare edge and the Apollo 16 site are compared to the numerically calculated model solutions. This comparison indicates that the anisotropic fluctuations can be modeled by a nonconducting layer in the lunar lithosphere which is 150 km thick beneath the highlands and 300 km thick beneath Mare Serenitatis. A decreased electrical conductivity in the upper mantle beneath the mare may be due to a lower temperature resulting from heat carried out the magma source regions to the surface during mare flooding.     

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.