U-Pb zircon dating of the lunar meteorite Dhofar 1442

Dhofar 1442 is one of the few lunar KREEP-rich meteorites, which contains KREEP norites and KREEP gabbronorite as well as low-Ti basalts and highly evolved granophyres. Zircon is a typical accessory mineral of KREEP rocks. U-Th-Pb dates of 12 zircon grains (four of them were in two lithic clasts, and the others were fragments in the meteorite matrix) indicate that the zircons belong to at least two groups of different age: “ancient” (～4.31 Ga) and “young” (～3.95 Ga), which correspond to two major pulses of KREEP magmatism in the source region of the Dhofar 1442 meteorite. The zircon of the “young” group was most probably related to the crater ejecta of the Mare Imbrium Basin. The rock fragments dated at approximately 3.95 Ga have the composition of KREEP gabbronorite. The parental rocks of the zircon of the “ancient” group in the Dhofar 1442 meteorite are uncertain and could be highly evolved granophyres. This hypothesis is supported by the high Th (100–300 ppm) and U (150–400 ppm) contents. These zircon fragments of the “ancient” group, higher than in the “young” group (<50 ppm Th and <70 ppm U) and are typical of zircon from lunar granitic rocks. The composition of the products of KREEP magmatism in the source region of the Dhofar 1442 meteorite could vary from predominantly granitic to KREEP gabbronoritic at 4.3–3.9 Ga.     

A Rb-Sr and Sm-Nd isotope geochronology and trace element study of lunar meteorite LaPaz Icefield 02205

Rubidium-strontium and samarium-neodymium isotopes of lunar meteorite LaPaz Icefield (LAP) 02205 are consistent with derivation of the parent magma from a source region similar to that which produced the Apollo 12 low-Ti olivine basalts followed by mixing of the magma with small amounts (1-2 wt%) of trace element-enriched material similar to lunar KREEP-rich sample SaU 169. The crystallization age of LAP 02205 is most precisely dated by an internal Rb-Sr isochron of 2991 ± 14 Ma, with an initial ⁸⁷Sr/⁸⁸Sr at the time of crystallization of 0.699836 ± 0.000010. Leachable REE-rich phosphate phases of LAP 02205 do not plot on a Sm-Nd mineral isochron, indicating contamination or open system behavior of the phosphates. Excluding anomalous phases from the calculation of a Sm-Nd isochron yields a crystallization age of 2992 ± 85 (initial ε¹⁴³Nd = +2.9 ± 0.8) that is within error of the Rb-Sr age, and in agreement with other independent age determinations for LAP 02205 from Ar-Ar and U-Pb methods. The calculated ¹⁴⁷Sm/¹⁴⁴Nd source ratios for LAP 02205, various Apollo 12 and 15 basalts, and samples with strong affinities to KREEP (SaU 169, NWA 773, 15386) are uncorrelated with their crystallization ages. This finding does not support the involvement of a common KREEP component as a heat source for lunar melting events that occurred after crystallization of the lunar magma ocean.     

月球同位素地质年代学与月球演化

同位素地质年代学是月球形成与演化研究的重要工具。目前对月岩和月球陨石的研究积累了大量的同位素年代学资料,其测试的主要方法包括K—Ar、Ar_Ar、Rh-sr、Sm—Nd、Lu—Hf、Re-0s、Pb—Pb和U—Pb等。根据目前获得的资料,本文对月球上不同类型岩石的形成年龄进行了总结,发现月球高地岩石主要形成于45～38亿年,而月海玄武岩相对年轻,大致形成于38～31亿年。根据这-年代资料,结合对月岩样品进行的短半衰期Hf-W与Sin-Nd同位素体系的研究结果,认为月球大致形成于45亿年,其后开始由岩浆海导致的内部核-幔-壳的分异,岩浆结晶的低密度斜长岩构成最初的月壳,而密度大的岩石构成月幔,而此月幔则成为后来月海玄武岩的主要岩浆源区。同时指出了当前月岩同位素地质年代学存在的问题,并根据技术进展的情况,对未来月岩同位素年代学的发展趋势作了全面的分析．     

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 H₂O 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 H₂O 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.     

A combined Sm-Nd, Rb-Sr, and U-Pb isotopic study of Mg-suite norite 78238: Further evidence for early differentiation of the Moon

Lunar Mg-suite norite 78238 was dated using the Sm-Nd, Rb-Sr, and U-Pb isotopic systems in order to constrain the age of lunar magma ocean solidification and the beginning of Mg-suite magmatism, as well as to provide a direct comparison between the three isotopic systems. The Sm-Nd isotopic system yields a crystallization age for 78238 of 4334 ± 37 Ma and an initial value of −0.27 ± 0.74. The age-initial (T-I) systematics of a variety of KREEP-rich samples, including 78238 and other Mg-suite rocks, KREEP basalts, and olivine cumulate NWA 773, suggest that lunar differentiation was completed by 4492 ± 61 Ma assuming a Chondritic Uniform Reservoir bulk composition for the Moon. The Rb-Sr isotopic systematics of 78238 were disturbed by post-crystallization processes. Nevertheless, selected data points yield two Rb-Sr isochrons. One is concordant with the Sm-Nd crystallization age, 4366 ± 53 Ma. The other is 4003 ± 95 Ma and is concordant with an Ar-Ar age for 78236. The ²⁰⁷Pb-²⁰⁶Pb age of 4333 ± 59 Ma is concordant with the Sm-Nd age. The U-Pb isotopic systematics of 78238 yield linear arrays equivalent to younger ages than the Pb-Pb system, and may reflect fractionation of U and Pb during sample handling. Despite the disturbed nature of the U-Pb systems, a time-averaged μ (²³⁸U/²⁰⁴Pb) value of the source can be estimated at 27 ± 30 from the Pb-Pb isotopic systematics. Because KREEP-rich samples are likely to be derived from source regions with the highest U/Pb ratios, the relatively low μ value calculated for the 78238 source suggests the bulk Moon does not have an exceedingly high μ value.     

Feldspathic lunar meteorites Pecora Escarpment 02007 and Dhofar 489: Contamination of the surface of the lunar highlands by post-basin impacts

PCA (Pecora Escarpment) 02007 and Dhofar 489 are both meteorites from the feldspathic highlands of the Moon. PCA 02007 is a feldspathic breccia consisting of lithified regolith from the lunar surface. It has concentrations of both incompatible and siderophile elements that are at the high end of the ranges for feldspathic lunar meteorites. Dhofar 489 is a feldspathic breccia composed mainly of impact-melted material from an unknown depth beneath the regolith. Concentrations of incompatible and siderophile elements are the lowest among brecciated lunar meteorites. Among 19 known feldspathic lunar meteorites, all of which presumably originate from random locations in the highlands, concentrations of incompatible elements like Sm and Th tend to increase with those of siderophile elements like Ir. Feldspathic meteorites with high concentrations of both suites of elements are usually regolith breccias. Iridium derives mainly from micrometeorites that accumulate in the regolith with duration of surface exposure. Micrometeorites have low concentrations of incompatible elements, however, so the correlation must reflect a three-component system. We postulate that the correlation between Sm and Ir occurs because the surface of the Feldspathic Highlands Terrane has become increasingly contaminated with time in Sm-rich material from the Procellarum KREEP Terrane that has been redistributed across the lunar surface by impacts of moderate-sized, post-basin impacts. The most Sm-rich regolith breccias among feldspathic lunar meteorites are about 3× enriched compared to the most Sm-poor breccias, but this level of enrichment requires only a few percent Sm-rich material typical of the Procellarum KREEP Terrane. The meteorite data suggest that nowhere in the feldspathic highlands are the concentrations of K, rare earths, and Th measured by the Lunar Prospector mission at the surface representative of the underlying “bedrock;” all surfaces covered by old regolith (as opposed to fresh ejecta) are at least slightly contaminated. Dhofar 489 is one of 15 paired lunar-meteorite stones from Oman (total mass of meteorite: 1037 g). On the basis of its unusually high Mg/Fe ratio, the meteorite is likely to have originated from northern feldspathic highlands.     

Early crustal building processes on the moon: Models for the petrogenesis of the magnesian suite

The plutonic rocks of the magnesian suite (Mg-suite) represent the period of lunar basaltic magmatism and crustal growth (∼4.46 to 4.1 Ga) that immediately followed the initial differentiation of the Moon by magma ocean (LMO) formation and crystallization. The volume and distribution of the Mg-suite and its petrogenetic relationship to latter stages of lunar magmatism (mare basalts) remains obscure. These plutonic rocks exhibit a range of compositions and include ultramafics, troctolites, spinel troctolites, norites, and gabbronorites. A distinguishing characteristic of this suite is that they contain some of the most magnesium-rich phases (Fo_95-90) that had crystallized from lunar magmas, yet they also are significantly enriched in an incompatible element component referred to as KREEP (a late-stage product of LMO crystallization containing abundant potassium (K), rare earth elements (REE), phosphorous (P), uranium, and thorium). Ion microprobe analyses of individual mineral phases (olivine, pyroxene, and plagioclase) from the Mg-suite have shown some very unexpected characteristics that have profound implications on the origin of these basaltic magmas. Although the Mg-suite lithologies are typified by silicates with relatively high Mg′, early liquidus phases such as olivine are fairly low in Ni, Co, and Cr relative to more iron-rich olivines in the younger mare basalts. The high Y and Ti/Y in early phases such as olivine and orthopyroxene indicate that the parental basaltic melts were high in incompatible elements and contained an “ilmenite fractionation” signature. However, the Y in olivine from many of the troctolites and ultramafic lithologies are only slightly greater than that of the olivine in the mare basalts whereas olivine in the norites, gabbronorites, and Apollo 14 troctolites are exceedingly high. The KREEP component may have been added to the Mg-suite parent magmas by assimilation or mixing into the mantle source. The volume of KREEP required to be added to the parental magmas of the Mg-suite tends to favor the latter mechanism for KREEP incorporation. The extremely high abundances of KREEP in the norites and gabbronorites are a product of substantial crystallization (40% to 70%) of KREEP-enriched Mg-suite parental magmas. Basaltic magmatism associated with KREEP extended for over 1.5 billion years and appears to have changed over time. The early stages of this style of lunar magmatism (Mg-suite) appear to represent melting of early LMO cumulates with low abundances of Ni, Co, Cr, and V. Later stages of KREEP-rich basaltic magmatism seemed to clearly involve melting of a variety of LMO cumulate assemblages with higher incompatible element enrichment. It appears that the heat derived from the KREEP component was instrumental in at least initiating melting of the lunar mantle over this period of time.     

Chemical composition of lunar meteorites and the lunar crust

The paper presents the first analyses of major and trace elements in 19 lunar meteorites newly found in Oman. These and literature data were used to assay the composition of highland, mare, and transitional (highland-mare interface) regions of the lunar surface. The databank used in the research comprises data on 44 meteorites weighing 11 kg in total, which likely represent 26 individual falls. Our data demonstrate that the lunar highland crust should be richer in Ca and Al but poorer in mafic and incompatible elements than it was thought based on studying lunar samples and the first orbital data. The Ir concentration in the highland crust and the analysis of lunar crater population suggest that most lunar impactites were formed by a single major impact event, which predetermined the geochemical characteristics of these rocks. Lunar mare regions should be dominated by low-Ti basalts, which are, however, enriched in LREEs compared to those sampled by lunar missions. The typical material of mare-highland interface zones can contain KREEP and magnesian VLT basalts. The composition of the lunar highland crust deduced from the chemistry of lunar meteorites does not contradict the model of the lunar magma ocean, but the average composition of lunar mare meteorites is inconsistent with this concept and suggests assimilation of KREEP material by basaltic magmas. The newly obtained evaluations of the composition of the highland crust confirm that the Moon can be enriched in refractory elements and depleted in volatile and siderophile elements.     

月球某些资源的开发利用前景

21世纪月球探测的主要趋势是建立月球基地，开发利用月球的矿产资源，能源和特殊环境，为人类社会的可持续发展发挥长期而有效的支撑作用，通过对月海玄武岩中的钛铁矿，克里普岩中的U，Th,REE和月壤中的拟－3在月面的含量与分布的系统分析，月海玄武碉中蕴藏有极丰富的钛铁矿，TiO2总资源量超过70万亿t，钛铁矿还是月球基地生产水和火箭燃料的主要原料；克里普岩是未来月球探测与研究的热点之一，其蕴藏有巨量的铀，钍，钾，磷和稀土元素资源；月壤长期受到太阳风的辐射，使其蕴藏有极其丰富的氢，氦，氧，氮等气体资源，其中氦－3的资源量大于100万t，它是一种可供人类社会长期使用的，安全，清洁，高效，廉价的核聚变发电燃料，其含量与月壤的化学成分，矿物组分，颗粒大小等有密切的关系。     

Mechanisms for incompatible-element enrichment on the Moon deduced from the lunar basaltic meteorite Northwest Africa 032

The lunar meteorite Northwest Africa (NWA) 032 is a low-Ti basalt that has incompatible-element abundances and Th/Sm ratios characteristic of the involvement of late stage magma ocean crystallization products (urKREEP) in its petrogenesis. This sample is very fine-grained and contains terrestrial weather products. A progressive leaching procedure was therefore developed and applied to magnetic separates and whole rock fractions to obtain Rb-Sr and Sm-Nd ages. Although many of the leachates, as well as the unleached mineral and whole rock fractions contain terrestrial alteration products, selected residue fractions yield concordant Rb-Sr and Sm-Nd ages. Rubidium-Sr isotopic analyses yield an age of 2947 ± 16 Ma with an initial ⁸⁷Sr/⁸⁶Sr of 0.700057 ± 17. These characteristics indicate NWA 032 is derived from a source region with an ⁸⁷Rb/⁸⁶Sr ratio of 0.044 ± 0.001. This value is higher than all but those determined for KREEP basalts, and suggests that NWA 032 is derived from a source region that has higher incompatible-element abundances than other low-Ti basalts. Samarium-neodymium isotopic analysis yield a concordant age of 2931 ± 92 Ma and an initial ε_Nd of +9.71 ± 0.74 corresponding to a source region with ¹⁴⁷Sm/¹⁴⁴Nd ratio of 0.246 ± 0.004. The initial Nd isotopic composition stands in contrast to the initial Sr isotopic composition by requiring NWA 032 to be derived from a source with lower incompatible-element abundances than most low-Ti basalts. The source of NWA 032 is therefore unlike those of other lunar basalts.Modeling of magma ocean cumulate formation demonstrates that unlike other low-Ti basalt source regions the NWA 032 source is a mixture of olivine, pigeonite, and clinopyroxene bearing cumulates and only a small amount of urKREEP. Furthermore, unlike other mare basalt sources, the NWA 032 source does not contain appreciable quantities of plagioclase. Partial melting models demonstrate that the incompatible-element characteristics of the NWA 032 result from formation by smaller degrees of partial melting than other mare basalts. Thus, the incompatible-element geochemical signature that is observed in NWA 032 appears to reflect the combined effects of generation from an unusual plagioclase-free incompatible-element-depleted source region by very small degrees of partial melting. This study demonstrates that both the presence of urKREEP in the source region and small degrees of partial melting generate magmas with similar, but not identical, incompatible-element characteristics. In addition, it underscores the fact that there is significantly more geochemical diversity on the Moon than is represented by samples collected by the American and Soviet lunar missions.     

Mineralogy, geochemistry, and Ar-Ar geochronology of lunar granulitic breccia Northwest Africa 3163 and paired stones: Comparisons with Apollo samples

The lunar meteorites Northwest Africa (NWA) 3163, 4881, and 4483 are paired stones classified as granulitic breccias. At 2.4 kg, these three stones constitute one of the largest known lunar meteorite masses. Here we describe the petrography, mineralogy, and chemistry of NWA 3163, 4881, and 4483, and present ⁴⁰Ar-³⁹Ar data for two of the meteorites. Two-pyroxene thermometry indicates that the rocks equilibrated at 1050 ± 50 °C, which represents the high-temperature, low-pressure event that generated their characteristic recrystallization textures and reset their Ar systematics. Stepped-heating, in situ infrared laser microprobe ⁴⁰Ar-³⁹Ar geochronology yields a mean age of 3327 ± 29 Ma for NWA 3163, and a more disturbed release spectrum for NWA 4881. NWA 4881 shows an upward-trending pattern, suggesting that it may have had a ⁴⁰Ar-³⁹Ar age of >3.0 Ga, but that it was partially reset at ∼2.6 Ga. NWA 3163 et al. exhibit shock effects, including maskelynitized plagioclase, shock veins, and melt pockets, which are absent in the Apollo granulitic breccias. Although the Apollo and meteorite samples are texturally similar and have comparable bulk compositions and equilibration temperatures, their trace and siderophile element contents point to distinct parental lithologies derived from different regions of the Moon. Based on mineralogical and geochemical differences between the Apollo and meteorite samples, we conclude that the parent rock(s) of the paired NWA meteorites came from an area outside the Imbrium region and that they underwent high-temperature (granulite event) metamorphism long after the Late Heavy Bombardment.     

Coupled Ce-Nd isotope systematics and rare earth elements differentiation of the moon

¹³⁸Ce/¹⁴²Ce and ¹⁴³Nd/¹⁴⁴Nd isotope ratios of lunar samples are determined to constrain the petrogenetic differentiation and evolution of the moon. High-precision Ce-Nd isotope data, well-defined Rb-Sr isochrons, and rare earth elements (REE) abundances of lunar samples show that unexpectedly low La/Ce ratios of evolved lunar highland samples are preserved from at least 3.9 Ga. Precise analysis of REE abundances indicates that the low La/Ce ratio results from a depletion of La relative to other REE. This depletion can be seen in pristine KREEP basalts and Mg-suite rocks from 3.85 to 4.46 Ga. As REE abundances of all these samples are controlled by the presence of a KREEP component, the depletion was probably inherited from a late crystallization sequence of the lunar magma ocean related to the production of the original KREEP component.     

Petrology, geochemistry, and age of low-Ti mare-basalt meteorite Northeast Africa 003-A: A possible member of the Apollo 15 mare basaltic suite

Northeast Africa 003 (NEA 003) is a lunar meteorite found as a two paired stones (6 and 118 g) in Libya, 2000 and 2001. The main portion (∼75 vol%) of the 118 g meteorite, used for this study, (NEA 003-A) consists of mare-basalt and a smaller adjacent portion (∼25 vol%) is a basaltic breccia (NEA 003-B). NEA 003-A has a coarse-grained magmatic texture consisting mainly of olivine, pyroxene and plagioclase. The late-stage mineral association is composed mainly of elongated plagioclase, ilmenite, troilite, fayalite, Si-K-rich glass, apatite, and a rare SiO₂ phase. Other accessory minerals include ulvöspinel, chromite, and trace Fe-Ni metal. Olivine and pyroxene contain shock-induced fractures, and plagioclase is completely converted into maskelynite.The Fe/Mn values of the whole rock, olivines and pyroxenes, and the bulk-rock oxygen isotopic composition provide evidence for the lunar origin of NEA 003-A meteorite. This is further supported by the presence of Fe-Ni metal and the anhydrous mineral association.NEA 003-A is geochemically and petrographically distinct from previously described mare-basalt meteorites and is not paired with any of them. The petrography and major element composition of NEA 003-A is similar to the composition of low-Ti olivine mare basalts from Apollo 12 and olivine-normative basalts from Apollo 15. The NEA 003-A meteorite shows obvious geochemical similarities in trace elements contents with Apollo 15 olivine-normative basalts and could represent a yet unknown geochemically primitive member of the olivine-normative basalt series. The meteorite is depleted in rare earth elements (REE) and incompatible trace elements indicating a primitive character of the parental magma. The bulk-rock chemical composition demonstrates that the parent melt of NEA 003-A was not contaminated with KREEP components as a result of magma mixing or assimilation processes. Results of crystallization modelling and low minimum cooling rate estimates (∼0.07 °C/h) suggest that the parent melt of NEA 003-A crystallized in the lower part of a lava flow containing cumulate olivine (∼10%) and was probably derived from more primitive picritic magma by fractional crystallization processes.Sm-Nd dating yields an age of 3.09 ± 0.06 Ga which corresponds to the period of lower Eratosthenian lunar volcanic activity, and the near-chondritic ε_Nd value of −0.4 ± 0.3 indicates that the meteorite could be derived from a slightly enriched mantle source similar to the Apollo 15 green glasses. Ar-Ar step release results are inconsistent with Sm-Nd ages suggesting that NEA 003-A was exposed to one or more impact events. The most extensive event took place at 1.8 Ga and the shock intensity was likely between 28 and 45 GPa. The absence of solar Ar suggests that NEA 003-A has not been directly exposed at the lunar surface but the cosmic ray exposure age of 209 ± 6 Ma suggests that NEA 003-A resided in the upper regolith for part of its history.     

SIMS U-Pb study of zircon from Apollo 14 and 17 breccias: Implications for the evolution of lunar KREEP

We report the results of a SIMS U-Pb study of 112 zircons from breccia samples from the Apollo 14 and 17 landing sites. Zircon occurs in the breccia matrices as rounded, irregular shaped, broken and rarely euhedral grains and as constituent minerals in a variety of lithic clasts ranging in composition from ultra-mafic and mafic rocks to highly evolved granophyres. Crystallisation of zircon in magmatic rocks is governed by the zirconium saturation in the melt. As a consequence, the presence of zircon in mafic rocks on the Moon implies enrichment of their parent melts in the KREEP component. Our SIMS results show that the ages of zircons from mafic to ultramafic clasts range from ca. 4.35 Ga to ca. 4.00 Ga demonstrating multiple generations of KREEPy mafic and ultramafic magmas over this time period. Individual zircon clasts in breccia matrices have a similar age range to zircons in igneous clasts and all represent zircons that have been incorporated into the breccia from older parents. The age distributions of zircons from breccias from both the Apollo 14 and Apollo 17 landing sites are essentially identical in the range 4.35-4.20 Ga. However, whereas Apollo 14 zircons additionally show ages from 4.20 to 3.90 Ga, no zircons from Apollo 17 samples have primary ages less than ca. 4.20 Ga. Also, in contrast to previous suggestions that the magmatism in the lunar crust is continuous our results show that the zircon age distribution is uneven, with distinct peaks of magmatic activity at ca. 4.35 Ga, ca. 4.20 Ga in Apollo 14 and 17 and a possible third peak in zircons from Apollo 14 at ca. 4.00 Ga. To explain the differences in the zircon age distributions between the Apollo 14 and 17 landing sites we propose that episodes of KREEP magmatism were generated from a primary reservoir, and that this reservoir contracted over time towards the centre of Procellarum KREEP terrane. We attribute the peaks in KREEP magmatism to impact induced emplacement of KREEP magma from a primary mantle source or to a progressive thermal build-up in the mantle source until the temperature exceeds the threshold for generation of KREEP magma, which is transported into the crust by an unspecified possibly plume-like process.     

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.     

Petrogenesis of the Apollo 14 high-alumina basalts: Implications from ion microprobe analyses

In this study, ion microprobe analyses of individual minerals are used to investigate the petrogenesis of the Apollo 14 high-Al basalts. We use trace element concentrations from individual minerals in the Apollo 14 high-Al basalts to evaluate both endogenic and exogenic models. The data show that if the Apollo 14 high-Al basalts were produced by melting within the lunar mantle, these basalts cannot be related to one another by closed-system fractional crystallization of a single basaltic melt. Rather, the trace element data show that variable amounts of a KREEP component were added to the basalts by either assimilation, mixing into mantle sources, or impact melting. Single-stage assimilation-fractional crystallization models can only explain the data from this study if an excessively large mass of urKREEP is assimilated into the parent magma before olivine crystallization. Alternatively, the trace element data can be explained if the Apollo 14 high-Al basalts were produced by melting multiple Al-rich mantle sources that contain different amounts of urKREEP. Finally, for impact melting to be a relevant process, the data require that multiple large impact melts be formed from mixed KREEP-rich target lithologies. The resulting impact melts must then crystallize to produce basalts with igneous textures, high Al₂O₃ concentrations, uniform major element compositions, and a wide range of incompatible trace element concentrations.     

Apollo 12 revisited

We present compositional data for 358 lithic fragments (2-4-mm size range) and 15 soils (<1-mm fines) from regolith samples collected at the Apollo 12 site. The regolith is dominated by mare basalt, KREEP impact-melt breccias (crystalline and glassy), and regolith breccias. Minor components include alkali anorthosite, alkali norite, granite, quartz monzogabbro, and anorthositic rocks from the feldspathic highlands. The typical KREEP impact-melt breccia of Apollo 12 (mean Th: 16 μg/g) is similar to that of the Apollo 14 site (16 μg/g), 180 km away. Both contain a minor component (0.3% at Apollo 12, 0.6% at Apollo 14) of FeNi metal that is dissimilar to metal in ordinary chondrites but is similar to metal found in Apollo 16 impact-melt breccias. The Apollo 12 regolith contains another variety of KREEP impact-melt breccia that differs from any type of breccia described from the Apollo sites in being substantially richer in Th (30 μg/g) but with only moderate concentrations of K. It is, however, similar in composition to the melt breccia lithology in lunar meteorite Sayh al Uhaymir 169. The average composition of typical mature soil corresponds to a mixture of 65% mare basalt, 20% typical KREEP impact-melt breccia, 7% high-Th impact-melt breccia, 6% feldspathic material, 2.6% alkali noritic anorthosite, and 0.9% CM chondrite. Thus, although the site was resurfaced by basaltic volcanism 3.1-3.3 Ga ago, a third of the material in the present regolith is of nonmare origin, mainly in the form of KREEP impact-melt breccias and glass. These materials occur in the Apollo 12 regolith mainly as a result of moderate-sized impacts into surrounding Fra Mauro and Alpes Formations that formed craters Copernicus (93 km diameter, 406 km distance), Reinhold (48 km diameter, 196 km distance), and possibly Lansberg (39 km diameter, 108 km distance), aided by excavation of basalt interlayers and mixing of regolith by small, local impacts. Anomalous immature soil samples 12024, 12032, and 12033 contain a lesser proportion of mare basalt and a correspondingly greater proportion of KREEP lithologies. These samples consist mainly of fossil or paleoregolith, likely ejecta from Copernicus, that was buried beneath the mixing zone of micrometeorite gardening, and then brought to the near surface by local craters such as Head, Bench, and Sharp Craters.     

Correlated δ18O and [Ti] in lunar zircons: a terrestrial perspective for magma temperatures and water content on the Moon

Zircon grains were separated from lunar regolith and rocks returned from four Apollo landing sites, and analyzed in situ by secondary ion mass spectrometry. Many regolith zircons preserve magmatic δ¹⁸O and trace element compositions and, although out of petrologic context, represent a relatively unexplored resource for study of the Moon and possibly other bodies in the solar system. The combination of oxygen isotope ratios and [Ti] provides a unique geochemical signature that identifies zircons from the Moon. The oxygen isotope ratios of lunar zircons are remarkably constant and unexpectedly higher in δ¹⁸O (5.61 ± 0.07 ‰ VSMOW) than zircons from Earth’s oceanic crust (5.20 ± 0.03 ‰) even though mare basalt whole-rock samples are nearly the same in δ¹⁸O as oceanic basalts on Earth (~5.6 ‰). Thus, the average fractionation of oxygen isotopes between primitive basalt and zircon is smaller on the Moon [Δ¹⁸O(WR-Zrc) = 0.08 ± 0.09 ‰] than on Earth (0.37 ± 0.04 ‰). The smaller fractionations on the Moon suggest higher temperatures of zircon crystallization in lunar magmas and are consistent with higher [Ti] in lunar zircons. Phase equilibria estimates also indicate high temperatures for lunar magmas, but not specifically for evolved zircon-forming melts. If the solidus temperature of a given magma is a function of its water content, then so is the crystallization temperature of any zircon forming in that melt. The systematic nature of O and Ti data for lunar zircons suggests a model based on the following observations. Many of the analyzed lunar zircons are likely from K, rare earth elements, P (KREEP)-Zr-rich magmas. Zircon does not saturate in normal mafic magmas; igneous zircons in mafic rocks are typically late and formed in the last most evolved portion of melts. Even if initial bulk water content is moderately low, the late zircon-forming melt can concentrate water locally. In general, water lowers crystallization temperatures, in which case late igneous zircon can form at significantly lower temperatures than the solidus inferred for a bulk-rock composition. Although lunar basalts could readily lose H₂ to space during eruption, lowering water fugacity; the morphology, large size, and presence in plutonic rocks suggest that many zircons crystallized at depths that retarded degassing. In this case, the crystallization temperatures of zircons are a sensitive monitor of the water content of the parental magma as well as the evolved zircon-forming melt. If the smaller Δ¹⁸O(zircon–mare basalt) values reported here are characteristic of the Moon, then that would suggest that even highly evolved zircon-forming magmas on the Moon crystallized at higher temperature than similar magmas on Earth and that magmas, though not necessarily water-free, were generally drier on the Moon.     

Lunar materials: Their mineralogy,petrology and chemistry

The manned Apollo 11, 12, 14 and 15 and the automated Luna 16 lunar missions have provided us with lunar rock and regolith (soil) samples from a number of geologically distinct sites. The mare regions were sampled by Apollo 11, 12 and Luna 16, whereas Apollo 14 landed on a terrain with more relief, the Fra Mauro Formation which represents an ejecta blanket from the Imbrian Basin, and Apollo 15 touched down near the lunar highlands. The samples collected consist of a mixture, mainly of basalt, breccia and regolith (soil-particulate matter, generally < 1 cm in size). The basalts show considerable variation in texture, mineralogy and chemistry and probably represent fragments from various parts of relatively thin and extensive lava flows in the maria. The breccias represent regolith material which was indurated to varying degrees by impact events. The regolith is a product of the breakdown, again by impact, of coherent rock masses of basalt and breccia.     

Petrology and geochemistry of LaPaz Icefield 02205: A new unique low-Ti mare-basalt meteorite

LaPaz Icefield 02205 (LAP 02205) is a new low-Ti mare-basalt meteorite that was discovered in the LaPaz Ice Field in Antarctica. This is the first crystalline lunar basalt in the US Antarctic collection and the only 5th unbrecciated mare-basalt meteorite to be discovered to date. The rock has a typical basaltic texture with tabular and elongated pyroxene and plagioclase crystals, and minor olivine grains commonly rimmed by pyroxenes. Core- to rim-zoning in terms of Fe and Mg is present in almost all pyroxene grains. Accessory minerals include ilmenite, chromite, ulvöspinel, troilite, and FeNi metal. This rock is highly enriched in late-stage mesostasis. Free silica is also abundant. In terms of texture and mineralogy, LAP 02205 displays features of low-Ti mare basalts, with similarities to some low-Ti Apollo 12 and Apollo 15 basalts. Whole-rock major- and trace-element compositions confirm the highly fractionated nature of this basalt. The whole-rock REE contents of the meteorite are the highest among all known low-Ti mare basalts. The platinum group element (PGE) contents in LAP are also enriched suggesting the possibility of endogenously enriched source regions or the PGEs generally behaved as incompatible elements during crystal fractionation under low fO₂ conditions. Trace-element contents of mineral grains in LAP 02205 display wide variations, suggesting extensive non-equilibrium crystallization. The REE concentrations in the earliest-formed minerals provide constraints on the composition of the parental liquid, which is similar to the measured whole-rock composition. Crystallization modeling of the LAP 02205 bulk composition yields a reasonable fit between predicted and observed mineral phases and compositions, except for the high-Mg olivine cores, which are observed in the rock but not predicted by the modeling. An isochron age of 2929 ± 150 Ma for phosphate minerals makes this rock one of the youngest lunar basalts known to date. The young age and specific geochemical characteristics of LAP distinguish it from those of most other low-Ti mare basalts. However, the low-Ti mare basalt meteorite, NWA 032, has a similar young age, and the two meteorites also appear to be closely related from some geochemical perspectives and might have originated from similar source regions on the Moon.