KREEP Component Research Articles

A sample of the Moon's far side retrieved by Chang'e-6 contains 2.83-billion-year-old basalt.

Remote sensing observations have shown that the far side of the Moon (lunar farside) has different geology and rock composition to the near side, including the abundances of potassium, rare earth elements, and phosphorus (collectively known as KREEP). The Chang'e-6 (CE-6) spacecraft collected samples from the South Pole-Aitken (SPA) basin on the farside and brought them to Earth. We use lead-lead and rubidium-strontium isotope systems to date low-titanium basalt in a CE-6 sample, finding a consistent age of 2830 ± 5 million years. We interpret this as the date of volcanism in SPA and incorporate it into lunar crater chronology. Strontium, neodymium and lead isotopes indicate the volcanic magma was from a lunar mantle source depleted in incompatible elements and containing almost no KREEP component.

Revisiting the formation of lunar anorthosites via the Rb[sbnd]Sr isotope systematics

The incorporation of KREEP (potassium, rare-earth element, and phosphorus), mantle-derived mafic melts and trapped liquid into the lunar ferroan anorthosite (FAN) suite plays a pivotal role in generating their geochemical and isotopic variations. Nonetheless, the specific involvement and distinct roles of these different components remain controversial. This study presents in-situ Sr isotopic data for 28 anorthositic clasts found within lunar feldspathic meteorites to trace their sources and post-modification processes. We find that these plagioclases exhibit substantial variations in their measured 87Sr/86Sr values (0.69978–0.70357), in contrast to the relatively narrow range observed in Apollo 16 FANs, thereby likely reflecting a diverse chemical composition of lunar crustal rocks. In contrast, the analyzed plagioclases have consistently low 87Rb/86Sr ratios (0.00185–0.03962), similar to those of Apollo samples, reflecting impact-induced loss of Rb. Detailed investigations indicate that certain elevated 87Sr/86Sr ratios are probably not caused by terrestrial contamination or instrumental analysis, but most likely result from the decay of 87Rb from sources with initial 87Rb/86Sr higher than 0.0119–0.1380. However, such elevated 87Rb/86Sr values cannot solely result from crystallization of the lunar magma ocean (LMO) and likely involve KREEP components. Combined with trace element data, we estimate the maximum proportion of KREEP melt in the formation of lunar anorthosites. Future analyses of lunar anorthosites collected by China's Chang'e-5 and Chang'e-6 missions will be crucial for validating the observed Sr isotopic heterogeneity.

Young KREEP-like mare volcanism from Oceanus Procellarum

The Moon’s mare volcanism predominantly occurs within the Procellarum KREEP Terrane (PKT), which is widely thought to be associated with KREEP components within the lunar interior. The Chang’e-5 (CE-5) mission sampled a young (2 Ga) mare basalt Em4/P58 unit of northern Oceanus Procellarum. The geochemistry of the CE-5 mare basalt enables assessment of mantle source compositions which are essential to understand the thermo-chemical mechanism for prolonged volcanism during secular cooling of the Moon. Geochemical compositions of the CE-5 bulk soil, breccias, and basalt clasts from various depths within the drill core consistently display high concentrations of incompatible trace elements (ITE: ∼ 0.3 × high-K KREEP; ∼ 5 μg/g Th) with KREEP-like inter-element ratios, for example for La/Sm, Nb/Ta, and Zr/Y. Exotic impact ejecta, extensive magma differentiation (<70 % fractional crystallization) and significant assimilation of KREEP materials during magma transit and eruption cannot account for the ITE contents and ratios or radiogenic isotope compositions (e.g., εNdinitial of + 8 to + 9 and εHfinitial of + 40 to + 46) of the CE-5 basalts; instead, partial melting of their mantle source played a dominant role. The Chang’e-5 basalt is a chemically evolved low-Ti mare basalt (Mg# of ∼ 34) with enriched KREEP-like ITE compositions but high long-term time-integrated Sm/Nd and Lu/Hf ratios, which represent a hitherto unsampled type of mare basalt. It formed by melting of an augite-rich mantle source (late-stage magma ocean cumulates containing > 30–60 % augite, and little or no ilmenite), with a small amount of late-stage interstitial melt that resembles KREEP (∼1–1.5 modal %, equivalent to 0.2–0.3 μg/g Th in the mantle source). The voluminous mare basalts making up the Em4/P58 unit (>1500 km3) provide compelling evidence for large-scale, ITE enriched young mare magmatism within Oceanus Procellarum. In combination with remote sensing data and with the unique Th-rich Apollo 12 basalt fragment 12032,366–18 (impact ejecta likely from Oceanus Procellarum), this implies that significant portions of the FeO- and Th-rich mare regions of the western PKT may also have formed in a similar way.

Elemental and Sr isotopic compositions of plagioclase as an indicator of lunar source-rock type: Insights from Chang'e 5 plagioclase fragments

Plagioclase is the most abundant mineral in lunar crustal rocks, and its elemental and Sr isotopic compositions vary among different lunar surface rock types, implying that plagioclase fragments in lunar regolith can be used to trace source-rock types. In this study, we measured major- and trace-elemental and RbSr isotopic compositions of plagioclase fragments from lunar soil returned by the Chang'e 5 (CE5) mission. Correlation between Sr and An contents allows the CE5 plagioclase fragments to be divided into three groups: normal-Sr (group A), high-Sr (group B), and low-Sr (group C). The similarity of elemental and RbSr isotopic compositions between plagioclase in groups A and B and plagioclase from CE5 basalt clasts indicates that plagioclase from groups A and B originated from the comminution of local CE5 basalt. Only two of the eighty-two analyzed plagioclases (∼2.4%) are classified as group C and have Sr isotopes that are distinct from those of groups A and B plagioclases, indicating an exotic origin. One group C plagioclase has a high 87Sr/86Sr ratio (0.70242) and content of rare earth elements and might have been derived from the Sharp B or Aristarchus craters, which are enriched in the KREEP component. The other group C plagioclase has much lower 87Sr/86Sr (0.69908) and a moderately high content of An (92.3) indicating an Mg-suite source rock and possible derivation from the Pythagoras crater. This study highlights the applicability of using elemental and Sr isotopic compositions of plagioclase fragments to trace the origin of lunar regolith.

Lunar Evolution in Light of the Chang'e-5 Returned Samples

The Chinese spacecraft Chang'e-5 (CE-5) landed on the northern Ocean Procellarum and returned 1,731 grams of regolith. The CE-5 regolith is composed mostly of fragments of basalt, impact glass, agglutinates, and mineral fragments. The basalts could be classified as of a low-Ti and highly fractionated type based on their TiO2 content of ∼5.3 wt% and Mg# of ∼28. Independent of petrographic texture, the CE-5 basalts have a uniform eruption age of 2,030 ± 4 Ma, demonstrating that the Moon remained volcanically active until at least ∼2.0 Ga. Although the CE-5 landing site lies within the so-called Procellarum KREEP [potassium (K), rare earth elements (REE), and phosphorus (P)] Terrane, neither the CE-5 basalts nor the mantle source regions of those basalts were enriched in KREEP components, such as incompatible elements, water, sulfur, or chlorine. Therefore, it would be a new and stimulating task in the future to look for the triggering mechanism of the young volcanism on the Moon. ▪The CE-5 spacecraft returned 1,731 grams of lunar regolith in December 2020. It was the first new lunar sample since the last collection in August 1976.▪CE-5 regolith is basaltic in chemical composition, with only ∼1% highland materials of anorthosite, Mg suite, alkali suite, and KREEP.▪The CE-5 basalt is low Ti and highly differentiated. It was extruded at ∼2.0 Ga, being the youngest lunar basalt identified so far from the Moon.▪The triggering mechanism of the ∼2.0 Ga lunar volcanism is not clearly understood because its mantle source was dry and contained low abundances of KREEP elements.

Complexity and ambiguity in the relationships between major lunar crustal lithologies and meteoritic clasts inferred from major and trace element modeling

Clasts of feldspathic lithologies such as magnesian anorthosites, anorthositic troctolites, and granulites in lunar meteorites have greatly expanded knowledge of the lithologic diversity of the lunar crust. However, their origins and relationships to other major crustal lithologies such as the ferroan anorthosites, magnesian-suite, and alkali-suite are not fully understood. Here we present the results of phase equilibrium modeling using the MELTS and MAGFOX programs designed to investigate the origins of lunar crustal lithologies and petrologic connections between them. We show that the major and trace element compositions of the Mg- and alkali-suites are consistent with partial melting of hybridized sources and are inconsistent with decompression melting + assimilation models. Our results also show that the vertical trend in Mg# in mafic silicates vs. An# in plagioclase characteristic of feldspathic meteoritic lithologies and ferroan anorthosites can be produced by fractional crystallization of KREEP-free Mg-suite melts, but that these melts are not likely to contribute significantly to the composition of the global crust. Furthermore, we calculated potential parental melt compositions for these crustal lithologies using the abundances of REEs in plagioclase in FANs, the Mg- and alkali-suites, and clasts in feldspathic meteorites. Our results show that despite low bulk rock abundances of incompatible trace elements in many feldspathic lunar meteorites, parental melts with overall REE abundances similar to or in excess of KREEP are needed to reproduce the REE abundances in plagioclase in clasts from feldspathic lunar meteorites. However, the lack of a Na enrichment trend in their plagioclase compositions with decreasing Mg# requires very Na-depleted melts without a KREEP component. The available data regarding magnesian anorthosites, anorthositic troctolites, and granulites in lunar meteorites, and inferences made here regarding their parental melt compositions, lead to contradictory and ambiguous conclusions regarding their origins.

A dunite fragment in meteorite Northwest Africa (NWA) 11421: A piece of the Moon’s mantle

Abstract A centimeter-sized fragment of dunite, the first recognized fragment of Moon mantle material, has been discovered in the lunar highlands breccia meteorite Northwest Africa (NWA) 11421. The dunite consists of 95% olivine (Fo83), with low-Ca and high-Ca pyroxenes, plagioclase, and chrome spinel. Mineral compositions vary little across the clast and are consistent with chemical equilibration. Mineral thermobarometry implies that the dunite equilibrated at 980 ± 20 °C and 0.4 ± 0.1 gigapascal (GPa) pressure. The pressure at the base of the Moon’s crust (density 2550 kg/m3) is 0.14–0.18 GPa, so the dunite equilibrated well into the Moon’s upper mantle. Assuming a mantle density of 3400 kg/m3, the dunite equilibrated at a depth of 88 ± 22 km. Its temperature and depth of equilibration are consistent with the calculated present-day selenotherm (i.e., lunar geotherm). The dunite’s composition, calculated from mineral analyses and proportions, contains less Al, Ti, etc., than chondritic material, implying that it is of a differentiated mantle (including cumulates from a lunar magma ocean). The absence of phases containing P, Zr, etc., suggests minimal involvement of a KREEP component, and the low proportion of Ti suggests minimal interaction with late melt fractionates from a lunar magma ocean. The Mg/Fe ratio of the dunite (Fo83) is significantly lower than models of an overturned unmixed mantle would suggest, but is consistent with estimates of the bulk composition of the Moon’s mantle.

Petrogenesis of Chang’E-5 mare basalts: Clues from the trace elements in plagioclase

AbstractThis study focuses on using the chemical compositions of plagioclase to further investigate the petrogenesis of Chang’E-5 young mare basalts and constrain its parental melt composition. Together with previously published data, our results show that the plagioclase in mare basalts overall displays large variations in major and trace element concentrations. Inversion of the plagioclase data indicates that the melt compositions parental to Chang’E-5 basalts have high rare earth elements (REE) concentrations similar to the high-K KREEP rocks (potassium, rare earth elements, and phosphorus). Such a signature is unlikely to result from the assimilation of KREEP components, because the estimated melt Sr shows positive correlations with other trace elements (e.g., Ba, La), which are far from the KREEP end-member. Instead, the nearly parallel REE distributions and a high degree of trace element enrichment in plagioclase indicate an extensive fractional crystallization process. Furthermore, the estimated melt REE concentrations from plagioclase are slightly higher than those from clinopyroxene, consistent with its relatively later crystallization. Using the Ti partition coefficient between plagioclase and melt, we estimated the parental melt TiO2 content from the earliest crystallized plagioclase to be ~3.3 ± 0.4 wt%, thus providing robust evidence for a low-Ti and non-KREEP origin for the Chang’E-5 young basalts in the Procellarum KREEP terrane.

Geochemistry of impact glasses in the Chang’e-5 regolith: Constraints on impact melting and the petrogenesis of local basalt

Lunar impact glasses can provide important information on the bulk compositions of their sources and the impact history of the Moon. Here, we report the chemical composition of fifty-four clean glass spherules containing neither relict clasts nor crystals from the Chang’e-5 (CE5) regolith. They can be subdivided into three compositional groups: (1) mid-Ti basaltic (TiO2 = 4.1 ∼ 6.5 wt%), (2) low-Ti basaltic (TiO2 = 1.3 ∼ 3.9 wt%), and (3) high-Al (Al2O3 > 15 wt%). Fifty-one glasses (∼94 %) are mid-Ti basaltic, which form a loose compositional cluster for most major and trace elements. These glasses exhibit considerable variations in SiO2 (35.3 ∼ 45.3 wt%). Their TiO2, Al2O3, MgO and CaO show negative correlations with SiO2, while the Na2O, K2O and P2O5 positively correlate with SiO2, also yielding a positive correlation between the CIPW normative plagioclase and olivine. These variations likely result from differential vaporization of SiO2, strongly suggesting an impact origin of these glasses. Their major and trace element compositions are averagely similar to the bulk-rock, in turn indicating that they were formed from the local regolith. The remaining three glasses, including two low-Ti basaltic and one high-Al variety, exhibit distinct major and trace elements from the regolith, indicating an exotic source. In addition, the mid-Ti basaltic glasses provide another approach for estimating the average composition of the CE5 basalt other than directly measuring the small basalt fragments assuming that the exotic materials in the CE5 regolith were limited. This estimation reveals critical trace element characteristics of the CE5 basalt, e.g., it has higher La/Yb (3.71), Sm/Yb (1.76), Sr/Yb (31.6), and (Eu/Eu*)N (0.45) than KREEP, indicating that CE5 basalt must derive from a non-KREEP source. Chemical modeling indicates that the contribution of KREEP-rich materials in the mantle source should be less than 0.3 %. The trace element characteristics of the CE5 basalt can be reproduced by extensive (80 %) fractional crystallization after low-degree (2 %) melting. We propose that this fractional crystallization process might occur at depth, implying vast igneous underplating (7,250 ∼ 11,750 km3) beneath the CE5 landing area. This study also suggests that the high Th concentration (5.43 ppm) is an inherent property of the CE5 basalt resulting from extensive fractional crystallization. Thus, high Th detected by remote sensing may not be associated directly with a KREEP component but rather with highly fractionated basalts.

Petrography, mineralogy, and geochemistry of a new lunar magnesian feldspathic meteorite Northwest Africa 11460

AbstractLunar meteorite Northwest Africa (NWA) 11460 has been classified as a polymict breccia, composed of feldspathic clasts, mafic‐rich clasts (gabbroic and troctolitic fragments), granulites, and a wide range of impact melt breccias and dimict breccias. The non‐mare clasts have chemical affinities in major element composition to the Apollo ferroan anorthosites (FAN) and magnesian‐suite plutonic rocks. In contrast, incompatible trace element (ITE) compositions of the Mg‐richer clasts are more consistent with those of FANs rather than magnesian‐suite rocks. NWA 11460 has a Mg‐rich feldspathic bulk composition (FeO = 4.53 wt%, Al2O3 = 25.87 wt%, and Mg# = 73.8) and relatively ITE‐poor (i.e., Th = 0.31 ppm and Sm = 0.65 ppm) characteristics. Feldspathic impact melt materials are approximately similar in composition to the estimated composition for the upper feldspathic lunar crust (as defined by Korotev et␣al., 2003). The ITE‐poor and Mg‐rich characteristics different from Apollo 16 feldspathic impact melts indicate that this meteorite has been possibly derived from a region distal to the nearside lunar highlands. Our analysis further suggests that NWA 11460 most likely originated from the farside of the Moon. Compositionally, Mg‐rich ITE‐poor clasts within NWA 11460 as well as those observed in other feldspathic lunar meteorites (which probably came from many different lunar regions) reveal that Mg‐rich rocks with low‐ITE components represent an important constituent of lunar crustal rocks. The diversities of highly magnesian non‐mare clasts and the low‐ITE chemistry provide geochemical clues for the genetic relationship between KREEP components and magnesian plutonic magmatism on the lunar farside.

The Cl isotope composition and halogen contents of Apollo-return samples

Lunar mare basalts are depleted in F and Cl by approximately an order of magnitude relative to mid-ocean ridge basalts and contain two Cl-bearing components with elevated isotopic compositions relative to the bulk-Earth value of ∼0‰. The first is a water-soluble chloride constituting 65 ± 10% of total Cl with δ37Cl values averaging 3.0 ± 4.3‰. The second is structurally bound chloride with δ37Cl values averaging 7.3 ± 3.5‰. These high and distinctly different isotopic values are inconsistent with equilibrium fractionation processes and instead suggest early and extensive degassing of an isotopically light vapor. No relationship is observed between F/Cl ratios and δ37Cl values, which suggests that lunar halogen depletion largely resulted from the Moon-forming Giant Impact. The δ37Cl values of apatite are generally higher than the structurally bound Cl, and ubiquitously higher than the calculated bulk δ37Cl values of 4.1 ± 4.0‰. The apatite grains are not representative of the bulk rock, and instead record localized degassing during the final stages of lunar magma ocean (LMO) or later melt crystallization. The large variability in the δ37Cl values of apatite within individual thin sections further supports this conclusion. While urKREEP (primeval KREEP [potassium/rare-earth elements/phosphorus]) has been proposed to be the source of the Moon's high Cl isotope values, the ferroan anorthosites (FANs) have the highest δ37Cl values and have a positive correlation with Cl content, and yet do not contain apatite, nor evidence of a KREEP component. The high δ37Cl values in this lithology are explained by the incorporation of a >30‰ HCl vapor from a highly evolved LMO.

The chlorine isotopic composition of the Moon: Insights from melt inclusions

The Moon exhibits a heavier chlorine (Cl) isotopic composition compared to the Earth. Several hypotheses have been put forward to explain this difference, based mostly on analyses of apatite in lunar samples complemented by bulk-rock data. The earliest hypothesis argued for Cl isotope fractionation during the degassing of anhydrous basaltic magmas on the Moon. Subsequently, other hypotheses emerged linking Cl isotope fractionation on the Moon with the degassing during the crystallization of the Lunar Magma Ocean (LMO). Currently, a variant of the LMO degassing model involving mixing between two end-member components, defined by early-formed cumulates, from which mare magmas were subsequently derived, and a KREEP component, which formed towards the end of the LMO crystallization, seems to reconcile some existing Cl isotope data on lunar samples. To further ascertain the history of Cl in the Moon and to investigate any evolution of Cl during magma crystallization and emplacement events, which could help resolve the chlorine isotopic variation between the Earth and the Moon, we analysed the Cl abundance and its isotopic composition in 36 olivine- and pyroxene-hosted melt inclusions (MI) in five Apollo basalts (10020, 12004, 12040, 14072 and 15016). Olivine-hosted MI have an average of 3.3±1.4ppm Cl. Higher Cl abundances (11.9 ppm on average) are measured for pyroxene-hosted MI, consistent with their formation at later stages in the crystallization of their parental melt compared to olivines. Chlorine isotopic composition (δ37Cl) of MI in the five Apollo basalts have weighted averages of +12.8±2.4‰ and +10.1±3.2‰ for olivine- and pyroxene-hosted MI, respectively, which are statistically indistinguishable. These isotopic compositions are also similar to those measured in apatite in these lunar basalts, with the exception of sample 14072, which is known to have a distinct petrogenetic history compared to other mare basalts. Based on our dataset, we conclude that, post-MI-entrapment, no significant Cl isotopic fractionation occurred during the crystallization and subsequent eruption of the parent magma and that Cl isotopic composition of MI and apatite primarily reflect the signature of the source region of these lunar basalts. Our findings are compatible with the hypothesis that in the majority of the cases the heavy Cl isotopic signature of the Moon was acquired during the earliest stages of LMO evolution. Interestingly, MI data from 14072 suggests that Apollo 14 lunar basalts might be an exception and may have experienced post-crystallization processes, possibly metasomatism, resulting in additional Cl isotopic fractionation recorded by apatite but not melt inclusions.

Ancient volcanism on the Moon: Insights from Pb isotopes in the MIL 13317 and Kalahari 009 lunar meteorites

Lunar meteorites provide a potential opportunity to expand the study of ancient (>4000 Ma) basaltic volcanism on the Moon, of which there are only a few examples in the Apollo sample collection. Secondary Ion Mass Spectrometry (SIMS) was used to determine the Pb isotopic compositions of multiple mineral phases (Ca-phosphates, baddeleyite K-feldspar, K-rich glass and plagioclase) in two lunar meteorites, Miller Range (MIL) 13317 and Kalahari (Kal) 009. These data were used to calculate crystallisation ages of 4332±2 Ma (95% confidence level) for basaltic clasts in MIL 13317, and 4369±7 Ma (95% confidence level) for the monomict basaltic breccia Kal 009. From the analyses of the MIL 13317 basaltic clasts, it was possible to determine an initial Pb isotopic composition of the protolith from which the clasts originated, and infer a 238U/204Pb ratio (μ-value) of 850±130 (2σ uncertainty) for the magmatic source of this basalt. This is lower than μ-values determined previously for KREEP-rich (an acronym for K, Rare Earth Elements and P) basalts, although analyses of other lithological components in the meteorite suggest the presence of a KREEP component in the regolith from which the breccia was formed and, therefore, a more probable origin for the meteorite on the lunar nearside. It was not possible to determine a similar initial Pb isotopic composition from the Kal 009 data, but previous studies of the meteorite have highlighted the very low concentrations of incompatible trace elements and proposed an origin on the farside of the Moon. Taken together, the data from these two meteorites provide more compelling evidence for widespread ancient volcanism on the Moon. Furthermore, the compositional differences between the basaltic materials in the meteorites provide evidence that this volcanism was not an isolated or localised occurrence, but happened in multiple locations on the Moon and at distinct times. In light of previous studies into early lunar magmatic evolution, these data also imply that basaltic volcanism commenced almost immediately after Lunar Magma Ocean (LMO) crystallisation, as defined by Nd, Hf and Pb model ages at about 4370 Ma.

Enigmatic cathodoluminescent objects in the Dhofar 025 lunar meteorite: Origin and sources

Dhofar 025 is a lunar highland breccia consisting mainly of anorthositic, with less common noritic, gabbronoritic, and troctolitic material. Rare fragments of low-Ti basalts are present as well, but no KREEP (component enriched in incompatible elements) was found in the meteorite. The cathodoluminescence study of this meteorite showed that its impact–melt matrix contains unusual cathodoluminescent (CL) objects of feldspathic composition, which frequently contain microlites of Fe-Mg spinel (pleonaste). They were presumably formed by impact mixing and melting of olivine and plagioclase with subsequent rapid quenching of the impact melts. Such mixing could happen either during assimilation of anorthosites by picritic/troctolitic magmas or during impact melting of troctolites. The enrichment of CL objects of Dhofar 025 in incompatible trace elements suggests that the mafic component of the impact mixture may be related to the high-magnesium suite rocks, which are frequently enriched in KREEP component. The depletion of CL objects in alkalis indicates their possible relation with residual glasses formed by evaporation. However, the presence of FeO in most objects points to the insignificant extent of evaporation. Thus, evaporation cannot explain the enrichment of the CL objects in Al2O3 and other refractory components, although this process definitely took place in their formation. Their similarity to the lunar pink spinel anorthosites, whose existence was predicted from orbital data, serves as an argument in support of the possible formation of the latters by impact mixing.

Petrology and geochemistry of feldspathic impact‐melt breccia Abar al' Uj 012, the first lunar meteorite from Saudi Arabia

AbstractAbar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al2O3, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An96.9Ab3.0Or0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm2 exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO2 than any mare basalt. It also has higher FeO and lower Al2O3 than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.

Phosphate-halogen metasomatism of lunar granulite 79215: Impact-induced fractionation of volatiles and incompatible elements

In the last decade, it has been recognized that the Moon contains significant proportions of volatile elements (H, F, Cl), and that they are transported through the lunar crust and across its surface. Here, we document a significant segment of that volatile cycle in lunar granulite breccia 79215: impact-induced remobilization of volatiles, and vapor-phase transport with extreme elemental fractionation. 79215 contains ~1% volume of fluorapatite, Ca_5(PO_4)_3(F,Cl,OH), in crystals to 1 mm long, which is reflected in its analyzed abundances of F, Cl, and P. The apatite has a molar F/Cl ratio of ~10, and contains only 25 ppm OH and low abundances of the rare earth elements (REE). The chlorine in the apatite is isotopically heavy, at δ^(37)Cl = +32.7 ± 1.6‰. Hydrogen in the apatite is heavy at δD = +1060 ± 180‰; much of that D came from spallogenic nuclear reactions, and the original δD was lower, between +350‰ and +700‰. Unlike other P-rich lunar rocks (e.g., 65015), 79215 lacks abundant K and REE, and other igneous incompatible elements characteristic of the lunar KREEP component. Here, we show that the P and halogens in 79215 were added to an otherwise “normal” granulite by vapor-phase metasomatism, similar to rock alteration by fumarolic exhalations as observed on Earth. The ultimate source of the P and halogens was most likely KREEP, it being the richest reservoir of P on the Moon, and 79215 having H and Cl isotopic compositions consistent with KREEP. A KREEP-rich rock was heated and devolatilized by an impact event. This vapor was fractionated by interaction with solid phases, including merrillite (a volatile-free phosphate mineral), a Fe-Ti oxide, and a Zr-bearing phase. These solids removed REE, Th, Zr, Hf, etc., from the vapor, and allowed the vapor to transport primarily P, F, and Cl, with lesser proportions of Ba and U into 79215. Vapor-deposited crystals of apatite (to 30 μm) are known in some lunar regolith samples, but lunar vapor has not (before this) been implicated in significant mass transfer. It seems unlikely, however, that phosphate-halogen metasomatism is related to the high-Th/Sm abundance ratios of this and other lunar magnesian granulites. The metasomatism of 79215 emphasizes the importance of impact heating in the lunar volatile cycle, both in mobilizing volatile components into vapor and in generating strong elemental fractionations.

Very high-K KREEP-rich clasts in the impact melt breccia of the lunar meteorite SaU 169: New constraints on the last residue of the Lunar Magma Ocean

In the impact melt breccia (IMB) of Sayh al Uhaymir (SaU) 169, the most KREEP-rich lunar meteorite to date (Gnos et al., 2004), clasts of a new type of lithologies were discovered, consisting of Ca-poor and Ca-rich pyroxenes (60.8vol.%), Ba-rich K-feldspar (27.9vol.%), phosphates (5.6vol.%), Nb-rich ilmenite (4.0vol.%), zircon (1.2vol.%) and minor sulfide (0.6vol.%). These mafic lithic clasts are more enriched in KREEP component (∼1500×CI) than the host meteorite and are highly enriched in potassium. They are referred to as very high-K (VHK) KREEP lithology, and probably most close to the last residual liquid of the Lunar Magma Ocean without significant dilution by other Mg-rich magmas. The fine-grained matrix of the SaU 169 IMB has very similar mineral chemistry to the VHK KREEP lithology, but contains abundant plagioclase with trace K-feldspar. The matrix shows decoupling of K from the REEP-like component; however, it cannot be simply interpreted by mixing the VHK KREEP lithology with anorthosites, which should have diluted the REEP-like component with the same proportion.SIMS Pb–Pb dating was conducted on zircons in various petrographic settings and with different crystal habits. All analyses show a main age peak at 3921±3Ma and a smaller one at 4016±6Ma. The main age peak is identical to the previous Pb–Pb age by Gnos et al. (2006) and U–Pb age by Liu et al. (2009), dating the catastrophic shock event contributed to the formation of SaU 169 IMB. The older ages are consistent with the previous report of an older bulk U–Pb age by Kramers et al. (2007), suggestive of presence of relict crystals in a few large zircon grains. The VHK KREEP clasts predated the fine-grained matrix, but have the same zircon Pb–Pb ages as the latter within the analytical uncertainties. Plagioclase was converted to maskelynite whereas zircon was shocked to diaplectic glass, probably by a second event at ∼2.8Ga. However, the identical zircon Pb–Pb ages of the amorphous parts and the remained crystalline areas indicate no resetting of Pb–Pb isotopes by the later shock metamorphism, or there was another severe impact event postdated solidification of the fine-grained matrix within a few million years.

Characterization of multiple lithologies within the lunar feldspathic regolith breccia meteorite Northeast Africa 001

Abstract– Lunar meteorite Northeast Africa (NEA) 001 is a feldspathic regolith breccia. This study presents the results of electron microprobe and LA‐ICP‐MS analyses of a section of NEA 001. We identify a range of lunar lithologies including feldspathic impact melt, ferroan noritic anorthosite and magnesian feldspathic clasts, and several very‐low titanium (VLT) basalt clasts. The largest of these basalt clasts has a rare earth element (REE) pattern with light‐REE (LREE) depletion and a positive Euanomaly. This clast also exhibits low incompatible trace element (ITE) concentrations (e.g., &lt;0.1 ppm Th, &lt;0.5 ppm Sm), indicating that it has originated from a parent melt that did not assimilate KREEP material. Positive Eu‐anomalies and such low‐ITE concentrations are uncharacteristic of most basalts returned by the Apollo and Luna missions, and basaltic lunar meteorite samples. We suggest that these features are consistent with the VLT clasts crystallizing from a parent melt which was derived from early mantle cumulates that formed prior to the separation of plagioclase in the lunar magma ocean, as has previously been proposed for some other lunar VLT basalts. Feldspathic impact melts within the sample are found to be more mafic than estimations for the composition of the upper feldspathic lunar crust, suggesting that they may have melted and incorporated material from the lower lunar crust (possibly in large basin‐forming events). The generally feldspathic nature of the impact melt clasts, lack of a KREEP component, and the compositions of the basaltic clasts, leads us to suggest that the meteorite has been sourced from the Outer‐Feldspathic Highlands Terrane (FHT‐O), probably on the lunar farside and within about 1000 km of sources of both Low‐Ti and VLT basalts, the latter possibly existing as cryptomaria deposits.

Fluorine and chlorine abundances in lunar apatite: Implications for heterogeneous distributions of magmatic volatiles in the lunar interior

Apatite has been analyzed from mare basalts, the magnesian-suite, the alkali-suite, and KREEP-rich impact-melt rocks using an electron probe microanalysis routine developed specifically for apatite. We determined that all the lunar apatite grains analyzed are predominantly fluorine rich; however, they also contain varying concentrations of chlorine and a missing structural component that, after ruling out other possibilities, we attribute to OH. Apatite grains from mare basalts are compositionally distinct from the apatite grains in the magnesian-suite, the alkali-suite, and KREEP-rich impact-melt rocks, which all had similar apatite compositions. Apatite grains in mare basalts are depleted in chlorine, and many of the analyzed grains have stoichiometry that suggests a significant OH component (i.e., >0.08 structural formula units), whereas apatite grains in the magnesian suite, alkali suite, and KREEP-rich impact melts are enriched in chlorine and do not typically have a missing structural component that could be attributed to OH − (within the detection limit of 0.08 sfu). From these data, we infer that residual liquids in the mare basalts were enriched in H 2O and fluorine relative to chlorine at the time of apatite crystallization, whereas residual liquids in magnesian-suite, alkali-suite, and KREEP-rich impact melts were enriched in chlorine relative to H 2O and fluorine at the time of apatite crystallization. The relative volatile abundance that we determined for the mare basalts is identical to the previously determined relative volatile abundance for the lunar picritic glasses. This result indicates that the observed relative volatile abundance signature of the picritic glass source is the same as that in the mare basalt source regions. The magnesian-suite, alkali-suite, and KREEP-rich impact-melt rocks likely reflect a volatile source with different volatile abundances than the sources of mare volcanics. Moreover, the magnesian-suite, alkali-suite, and KREEP-rich impact-melt rocks may reveal the relative volatile abundance of urKREEP, the residual melt of the magma ocean. This difference in relative magmatic volatile abundance among the lithologic groups investigated cannot be explained by degassing of a single source composition (relative to magmatic volatiles). The most reasonable explanation for the compositional disparity is a difference in the relative volatile abundances in the magmatic source regions of the Moon. Therefore, we conclude that the Moon has a heterogeneous distribution of magmatic volatiles within its interior, with a chemical divide (with respect to magmatic volatiles) existing between magmas that arise by partial melting of the lunar mantle and magmas that have seen significant contamination by a KREEP component.

Overview of Elemental Distributions on the Moon Observed by SELENE GRS

The high precision gamma-ray spectrometer (GRS) is carried on the first Japan's large-scaled lunar explorer, SELENE (KAGUYA) circling a polar orbit. The GRS consists of a large Ge crystal as a main detector and massive bismuth germanate crystals and a plastic scintillator as anticoincidence detectors. Since the successful launch on Sep. 14, 2007, radiation damage in the Ge detector has been induced from the incidence of energetic particles from space, which degraded its energy resolution. Then the Ge detector was annealed for 2 days at 85±5 K and the resolution is recovered to the level at the initial phase of the early observation. The special operations were conducted in December, 2008 in order to measure backgrounds gamma rays from the materials of the spacecraft body and the GRS instrument itself. The GRS data from the 100 km altitude reveal the global distribution of trace elements of Th and K on the Moon which delineates the distributions of KREEP component of lunar materials. Th and K-rich materials are concentrated around the Imbrium basin in Procellarum KREEP Terrane (PKT) and intermediately concentrated in South Pole–Aitken basin area on the farside. Results from special operations and observation are described and discussed.