Lunar meteorite LaPaz Icefield 04841: Petrology,texture, and impact‐shock effects of a low‐Ti mare basalt

Abstract— Found during the 2004 U.S. Antarctic Search for Meteorites season, LaPaz Icefield (LAP) 04841 represents an addition to the LaPaz lunar basalts suite and brings the total mass collected to 1.93 kg. The presence of FeNi grains, troilite, and the anorthositic composition of plagioclase are evidence for the lunar origin of this meteorite. Pyroxene and olivine Mn/Fe values plot along the trend set for lunar basalts. Analyses of chromite grains provide a V/(Al + Cr) ratio of 1.33 ± 13, translating to an fO₂ one log unit below the IW buffer, in accordance with previous fO₂ estimates for lunar basalts. Application of the Zr‐cooling speedometer, for ilmenite and ulvöspinel pairs, gives a cooling rate of 5.2 °C/day, matching previous estimates of cooling rates for the LaPaz lunar meteorites and Apollo mare basalts. Mineral modes and chemistries, as well as trace‐element patterns, provide compelling evidence for pairing of this meteorite to others in the LaPaz lunar basalt suite.     

H and Cl isotope systematics of apatite in brecciated lunar meteorites Northwest Africa 4472, Northwest Africa 773, Sayh al Uhaymir 169, and Kalahari 009

We have investigated the H and Cl systematics in apatite from four brecciated lunar meteorites. In Northwest Africa (NWA) 4472, most of the apatites contain ～2000–6000 ppm H₂O with δD between ?200 and 0‰, except for one grain isolated in the matrix, which contains ～6000 ppm H₂O with δD of ～500–900‰. This low‐δD apatite contains ～2500–7500 ppm Cl associated with δ³⁷Cl of ～15–20‰, while the high‐δD grain contains ～2500 ppm Cl with δ³⁷Cl of ～7–15‰. In NWA 773, apatites in a first group contain ～700–2500 ppm H₂O with δD values averaging around ～0 ± 100‰, while apatites in a second group contain ～5500–16500 ppm H₂O with δD ～250 ± 50‰. In Sayh al Uhaymir (SaU) 169 and Kalahari (Kal) 009, apatites are similar in terms of their H₂O contents (～600–3000 ppm) and δD values (?100 to 200‰). In SaU 169, apatites contain ～6000–10,000 ppm Cl, characterized by δ³⁷Cl of ～5–12‰. Overall, most of the analyzed apatite grains have δD within the range reported for carbonaceous chondrites, similar to apatite analyzed in ancient (>3.9 Ga) lunar magmatic. One grain in NWA 4472 has H and Cl isotope compositions similar to apatite from mare basalts. With an age of 4.35 Ga, this grain could be a representative of the oldest known lunar volcanic activity. Finally, since numerous evolved clasts in NWA 773 formed through silicate liquid immiscibility, the apatite grains with extremely high H₂O contents, reaching pure hydroxylapatite composition, could provide insights into the effects of such process on the evolution of volatiles in lunar magmas.     

Petrography and geochemistry of five new Apollo 16 mare basalts and evidence for post‐basin deposition of basaltic material at the site

Abstract— We present the petrography and geochemistry of five 2–4 mm basalt fragments from the Apollo 16 regolith. These fragments are 1) a high‐Ti vitrophyric basalt compositionally similar to Apollo 17 high‐Ti mare basalts, 2) a very high‐Ti vitrophyric basalt compositionally similar to Apollos 12 and 14 red‐black pyroclastic glass, 3) a coarsely crystalline high‐Al basalt compositionally similar to group 5 Apollo 14 high‐Al mare basalts, 4) a very low‐Ti (VLT) crystalline basalt compositionally similar to Luna 24 VLT basalts, and 5) a VLT basaltic glass fragment compositionally similar to Apollo 17 VLT basalts. High‐Ti basalt has been reported previously at the Apollo 16 site; the other basalt types have not been reported previously. As there are no known cryptomaria or pyroclastic deposits in the highlands near the Apollo 16 site (ruling out a local origin), and scant evidence for basaltic material in the Apollo 16 ancient regolith breccias or Apollo 16 soils collected near North Ray Crater (ruling out a basin ejecta origin), we infer that the basaltic material in the Apollo 16 regolith originated in maria near the Apollo 16 site and was transported laterally to the site by small‐ to medium‐sized post‐basin impacts. On the basis of TiO₂ concentrations derived from the Clementine UVVIS data, Mare Tranquillitatis (?300 km north) is the most likely source for the high‐Ti basaltic material at the Apollo 16 site (craters Ross, Arago, Dionysius, Maskelyne, Moltke, Sosigenes, Schmidt), Mare Nectaris/Sinus Asperitatis (?220 km east) is the most likely source for the low‐Ti and VLT basaltic material (craters Theophilus, Madler, Torricelli), and a large regional pyroclastic deposit near Mare Vaporum (?600 km northwest) is the most likely source region for pyroclastic material (although no source craters are apparent in the region).     

The Hadley‐Apennine KREEP basalt igneous province

Abstract– We have studied 27 KREEP basalt fragments in six thin sections of samples collected from four Apollo 15 stations. Based on local geology and regional remote sensing data, these samples represent KREEP basalt lava flows that lie beneath the younger, local Apollo 15 mare basalts and under other mare flows north of the Apollo 15 site. Some of these rocks were deposited at the site as ejecta from the large craters Aristillus and Autolycus. KREEP basalts in this igneous province have a volume of 10³–2 × 10⁴ km³. Mineral and bulk compositional data indicate that the erupted magmas had Mg# [100 × molar Mg/(Mg + Fe)] up to 73, corresponding to orthopyroxene‐rich interior source regions with Mg# up to 90. Minor element variations in the parent magmas of the KREEP basalts, inferred from compositions of the most magnesian pyroxene and most calcic plagioclase in each sample, indicate small but significant differences in the concentrations of minor elements and Mg#, reflecting variations in the composition of lower crustal or mantle source regions and/or different amounts of partial melting of those source regions.     

Searching for nonlocal lithologies in the Apollo 12 regolith: A geochemical and petrological study of basaltic coarse fines from the Apollo lunar soil sample 12023,155

New data from a petrological and geochemical examination of 12 coarse basaltic fines from the Apollo 12 soil sample 12023,155 provide evidence of additional geochemical diversity at the landing site. In addition to the bulk chemical composition, major, minor, and trace element analyses of mineral phases are employed to ascertain how these samples relate to the Apollo 12 lithological basalt groups, thereby overcoming the problems of representativeness of small samples. All of the samples studied are low‐Ti basalts (0.9–5.7 wt% TiO₂), and many fall into the established olivine, pigeonite, and ilmenite classification of Apollo 12 basaltic suites. There are five exceptions: sample 12023,155_1A is mineralogically and compositionally distinct from other Apollo 12 basalt types, with low pigeonite REE concentrations and low Ni (41–55 ppm) and Mn (2400–2556 ppm) concentrations in olivine. Sample 12023,155_11A is also unique, with Fe‐rich mineral compositions and low bulk Mg# (=100 × atomic Mg/[Mg+Fe]) of 21.6. Sample 12023,155_7A has different plagioclase chemistry and crystallization trends as well as a wider range of olivine Mg# (34–55) compared with other Apollo 12 basalts, and shows greater similarities to Apollo 14 high‐Al basalts. Two other samples (12023,155_4A, and _5A) are similar to the Apollo 12 feldspathic basalt 12038, providing additional evidence that feldspathic basalts represent a lava flow proximal to the Apollo 12 site rather than material introduced by impacts. We suggest that at least one parent magma, and possibly as many as four separate parent magmas, are required in addition to the previously identified olivine, pigeonite, and ilmenite basaltic suites to account for the observed chemical diversity of basalts found in this study.     

The origin of young mare basalts inferred from lunar meteorites Northwest Africa 4734, 032, and LaPaz Icefield 02205

Northwest Africa (NWA) 4734 is an unbrecciated basaltic lunar meteorite that is nearly identical in chemical composition to basaltic lunar meteorites NWA 032 and LaPaz Icefield (LAP) 02205. We have conducted a geochemical, petrologic, mineralogic, and Sm‐Nd, Rb‐Sr, and Ar‐Ar isotopic study of these meteorites to constrain their petrologic relationships and the origin of young mare basalts. NWA 4734 is a low‐Ti mare basalt with a low Mg* (36.5) and elevated abundances of incompatible trace elements (e.g., 2.00 ppm Th). The Sm‐Nd isotope system dates NWA 4734 with an isochron age of 3024 ± 27 Ma, an initial ε_Nd of +0.88 ± 0.20, and a source region ¹⁴⁷Sm/¹⁴⁴Nd of 0.201 ± 0.001. The crystallization age of NWA 4734 is concordant with those of LAP 02205 and NWA 032. NWA 4734 and LAP 02205 have very similar bulk compositions, mineral compositions, textures, and ages. Their source region ¹⁴⁷Sm/¹⁴⁴Nd values indicate that they are derived from similar, but distinct, source materials. They probably do not sample the same lava flow, but rather are similarly sourced, but isotopically distinct, lavas that probably originate from the same volcanic complex. They may have experienced slightly different assimilation histories in route to eruption, but can be source‐crater paired. NWA 032 remains enigmatic, as its source region ¹⁴⁷Sm/¹⁴⁴Nd definitively precludes a simple relationship with NWA 4734 and LAP 02205, despite a similar bulk composition. Their high Ti/Sm, low (La/Yb)_N, and Cl‐poor apatite compositions rule out the direct involvement of KREEP. Rather, they are consistent with low‐degree partial melting of late‐formed LMO cumulates, and indicate that the geochemical characteristics attributed to urKREEP are not unique to that reservoir. These and other basaltic meteorites indicate that the youngest mare basalts originate from multiple sources, and suggest that KREEP is not a prerequisite for the most recent known melting in the Moon.     

The evolution of the lunar Nectaris multiring basin

Nectaris is an 820-km-diameter, multiring impact basin located on the near side of the Moon. The transient cavity is estimated to have been less than 90 km in depth and materials were excavated from a depth of less than 30 km. About 2 km thickness of impact melt is believed to line the cavity center. The impact event probably took place at about 3.98 ± 0.03 × 10⁹ years ago. Nectaris ejecta forms a substantial proportion of the surface materials at the Apollo 16 site. Inter-ring plains deposits were deposited after the formation of the Nectaris basin. The most persuasive origin for the smooth plains is one of extrusives overlain by a thin veneer of ejecta. Basaltic fragments within Apollo 16 samples are believed to have been largely derived from Nectaris. A titanium-rich Apollo 16 mare basalt fragment has an age of 3.79 ± 0.05 × 10⁹ years but, although some relatively titanium-enriched basalts occur in southern Nectaris, titanium-rich basalts are nowhere seen at the surface of the mare. The earliest recognized eruptives appear to be low-titanium (perhaps VLT) basalts found as pyroclastic materials on Daguerre and in the Gaudibert region. The majority of the surface basalts are of intermediate composition (possibly similar to Apollo 12 basalts) and have an age of approximately 3.6 × 10⁹ years. The basalt fill is estimated to have a minimum thickness of 3 km. Flood-style eruptions appear to have been the main form of extrusion. Mare ridges exhibit a strong north-south preferential alignment and appear to postdate basalt emplacement. The lack of basin-related graben in Nectaris is consistent with a thick lithosphere. The basin ring structure is best preserved in the southwest and least preserved in the northeast. This is believed to result from horizontal variations in the crust and lithosphere thicknesses and from the influence of the preexisting Fecunditatis and Tranquillitatis basins; the ring structure is best preserved where the lithosphere was thickest. Floor-fractured craters within Nectaris are intimately associated with the basalt fill both in terms of age and location. Theophilus ejecta, small craters, and Tycho rays, combined with subsidence and mare ridge development, were the only modifying influences on Nectaris since the termination of basalt eruptions.     

The fate of moderately volatile elements in impact events—Lithium connection between the Ries sediments and central European tektites

Lithium abundances and isotope compositions are presented for a suite of sediments from the surroundings of the Ries Impact structure, paralleled by new Li data for central European tektites (moldavites) from several substrewn fields (South Bohemia, Moravia, Cheb Basin, Lusatia), including a specimen from the newly discovered substrewn field in Poland. The data set was supplemented by three clay fractions isolated from sedimentary samples. Moldavites measured in this study show a very narrow range in δ⁷Li values (?0.6 to 0.3‰ relative to L‐SVEC) and Li contents (23.9–48.1 ppm). This contrasts with sediments from the Ries area which show remarkable range in Li isotope compositions (from ?6.9 to 13.4‰) and Li contents (0.6–256 ppm). The OSM sediments which, based on chemical similarity, formed the major part of moldavites, show a range in δ⁷Li values from ?2.0 to 7.9‰ and Li contents from 5.8 to 78.9 ppm. Therefore, the formation of moldavites was apparently accompanied by large‐scale mixing, paralleled by chemical and isotope homogenization of their parent matter. The proposed Li mixing model indicates that sands, clayey sediments, and low volumes of carbonates are the major components for tektite formation whereas residual paleokarst sediments could have been a minor but important component for a subset of moldavites. Striking homogenization of Li in tektites, combined with limited Li loss during impacts, may suggest that moderately volatile elements are not scavenged and isotopically fractionated during large‐scale collisions, which is consistent with recent models. In general, whether homogenization of bodies with distinct Li isotope systematics takes place, or collision of bodies with similar Li systematics operates cannot be resolved at present stage but Li isotope homogeneity of solar system planets and asteroidal bodies tentatively implies the latter.     

Homogeneous distribution of Fe isotopes in the early solar nebula

To examine the iron (Fe) isotopic heterogeneities of CI and ordinary chondrites, we have analyzed several large chips (approximately 1 g) from three CI chondrites and three ordinary chondrites (LL5, L5, and H5). The Fe isotope compositions of five different samples of Orgueil, one from Ivuna and one from Alais (CI chondrites), are highly homogeneous. This new dataset provides a δ⁵⁶Fe average of 0.02 ± 0.04‰ (2SE, n = 7), which represents the best available value for the Fe isotopic composition of CI chondrites and probably the best estimate of the bulk solar system. We conclude that the homogeneity of CI chondrites reflects the initial Fe isotopic homogeneity of the well‐mixed solar nebula. In contrast, larger (up to 0.26‰ in δ⁵⁶Fe) isotopic variations have been found between separate approximately 1 g pieces of the same ordinary chondrite sample. The Fe isotope heterogeneities in ordinary chondrites appear to be controlled by the abundances of chondritic components, specifically chondrules, whose Fe isotope compositions have been fractionated by evaporation and recondensation during multiple heating events.     

The regolith portion of the lunar meteorite Sayh al Uhaymir 169

Abstract— –Sayh al Uhaymir (SaU) 169 is a composite lunar meteorite from Oman that consists of polymict regolith breccia (8.44 ppm Th), adhering to impact‐melt breccia (IMB; 32.7 ppm Th). In this contribution we consider the regolith breccia portion of SaU 169, and demonstrate that it is composed of two generations representing two formation stages, labeled II and III. The regolith breccia also contains the following clasts: Ti‐poor to Ti‐rich basalts, gabbros to granulites, and incorporated regolith breccias. The average SaU 169 regolith breccia bulk composition lies within the range of Apollo 12 and 14 soil and regolith breccias, with the closest correspondence being with that of Apollo 14, but Sc contents indicate a higher portion of mare basalts. This is supported by relations between Sm‐Al₂O₃, FeO‐Cr₂O₃‐TiO₂, Sm/Eu and Th‐K₂O. The composition can best be modeled as a mixture of high‐K KREEP, mare basalt and norite/troctolite, consistent with the rareness of anorthositic rocks. The largest KREEP breccia clast in the regolith is identical in its chemical composition and total REE content to the incompatible trace‐element (ITE)‐ rich high‐K KREEP rocks of the Apollo 14 landing site, pointing to a similar source. In contrast to Apollo 14 soil, SaU 169 IMB and SaU 169 KREEP breccia clast, the SaU 169 regolith is not depleted in K/Th, indicating a low contribution of high‐Th IMB such as the SaU 169 main lithology in the regolith. The data presented here indicate the SaU 169 regolith breccia is from the lunar front side, and has a strong Procellarum KREEP Terrane signature.     

Silicon and iron isotopes in components of enstatite chondrites: Implications for metal–silicate–sulfide fractionation in the solar nebula

Silicon and iron isotope compositions of different physically separated components of enstatite chondrites (EC) were determined in this study to understand the role of nebular and planetary scale events in fractionating Si and Fe isotopes of the terrestrial planet-forming region. We found that the metal–sulfide nodules of EC are strongly enriched in light Si isotopes (δ³⁰Si ≥ −5.61 ± 0.12‰, 2SD), whereas the δ³⁰Si values of angular metal grains, magnetic, slightly magnetic, and non-magnetic fractions become progressively heavier, correlating with their Mg# (Mg/(Mg+Fe)). White mineral phases, composed primarily of SiO₂ polymorphs, display the heaviest δ³⁰Si of up to +0.23 ± 0.10‰. The data indicate a key role of metal–silicate partitioning on the Si isotope composition of EC. The overall lighter δ³⁰Si of bulk EC compared to other planetary materials can be explained by the enrichment of light Si isotopes in EC metals along with the loss of isotopically heavier forsterite-rich silicates from the EC-forming region. In contrast to the large Si isotope heterogeneity, the average Fe isotope composition (δ⁵⁶Fe) of EC components was found to vary from −0.30 ± 0.08‰ to +0.20 ± 0.04‰. A positive correlation between δ⁵⁶Fe and Ni/S in the components suggests that the metals are enriched in heavy Fe isotopes whereas sulfides are the principal hosts of light Fe isotopes in the non-magnetic fractions of EC. Our combined Si and Fe isotope data in different EC components reflect an inverse correlation between δ³⁰Si and δ⁵⁶Fe, which illustrates that partitioning of Si and Fe among metal, silicate, and sulfidic phases has significantly fractionated Si and Fe isotopes under reduced conditions. Such isotope partitioning must have occurred before the diverse components were mixed to form the EC parent body. Evaluation of diffusion coefficients of Si and Fe in the metal and non-metallic phases suggests that the Si isotope compositions of the silicate fractions of EC largely preserve information of their nebular processing. On the other hand, the Fe isotopes might have undergone partial or complete re-equilibration during parent body metamorphism. The relatively uniform δ⁵⁶Fe among different types of bulk chondrites and the Earth, despite Fe isotope differences among their components, demonstrates that the chondrite parent bodies were not formed by random mixing of chondritic components from different locations in the disk. Instead, the chondrite components mostly originated in the same nebular reservoir and Si and Fe isotopes were fractionated either due to gas–solid interactions and associated changes in physicochemical environment of the nebular reservoir and/or during parent body processing. The heavier Si isotope composition of the bulk silicate Earth may require accretion of chondritic and/or isotopically heavier EC silicates along with cumulation of refractory forsterite-rich heavier silicates lost from the EC-forming region to form the silicate reservoir of the Earth.     

Petrography and geochemistry of the LaPaz Icefield basaltic lunar meteorite and source crater pairing with Northwest Africa 032

Abstract— We report on the bulk composition and petrography of four new basaltic meteorites found in Antarctica—LAP (LaPaz Icefield) 02205, LAP 02224, LAP 02226, and LAP 02436—and compare the LAP meteorites to other lunar mare basalts. The LAP meteorites are coarse‐grained (up to 1.5 mm), subophitic low‐Ti basalts composed predominantly of pyroxene and plagioclase, with minor amounts of olivine, ilmenite, and a groundmass dominated by fayalite and cristobalite. All of our observations and results support the hypothesis that the LAP stones are mutually paired with each other. In detail, the geochemistry of LAP is unlike those of any previously studied lunar basalt except lunar meteorite NWA (Northwest Africa) 032. The similarities between LAP and NWA 032 are so strong that the two meteorites are almost certainly source crater paired and could be two different samples of a single basalt flow. Petrogenetic modeling suggests that the parent melt of LAP (and NWA 032) is generally similar to Apollo 15 low‐Ti, yellow picritic glass beads, and that the source region for LAP comes from a similar region of the lunar mantle as previously analyzed lunar basalts.     

KREEPy lunar meteorite Dhofar 287A: A new lunar mare basalt

Abstract— Dhofar 287 (Dho 287) is a new lunar meteorite, found in Oman on January 14, 2001. The main portion of this meteorite (Dho 287A) consists of a mare basalt, while a smaller portion of breccia (Dho 287B) is attached on the side. Dho 287A is only the fourth crystalline mare basalt meteorite found on Earth to date and is the subject of the present study. The basalt consists mainly of phenocrysts of olivine and pyroxene set in a finer‐grained matrix, which is composed of elongated pyroxene and plagioclase crystals radiating from a common nucleii. The majority of olivine and pyroxene grains are zoned, from core to rim, in terms of Fe and Mg. Accessory minerals include ilmenite, chromite, ulvöspinel, troilite, and FeNi metal. Chromite is invariably mantled by ulvöspinel. This rock is unusually rich in late‐stage mesostasis, composed largely of fayalite, Si‐K‐Ba‐rich glass, fluorapatite, and whitlockite. In texture and mineralogy, Dho 287A is a low‐Ti mare basalt, with similarities to Apollo 12 (A‐12) and Apollo 15 (A‐15) basalts. However, all plagioclase is now present as maskelynite, and its composition is atypical for known low‐Ti mare basalts. The Fe to Mn ratios of olivine and pyroxene, the presence of FeNi metal, and the bulk‐rock oxygen isotopic ratios, along with several other petrological features, are evidence for the lunar origin for this meteorite. Whole‐rock composition further confirms the similarity of Dho 287A with A‐12 and A‐15 samples but requires possible KREEP assimilation to account for its rare‐earth‐element (REE) contents. Cooling‐rate estimates, based on Fo zonation in olivine, yield values of 0.2–0.8°C/hr for the lava, typical for the center of a 10–20 m thick flow. The recalculated major‐element concentrations, after removing 10–15% modal olivine, are comparable to typical A‐15 mare basalts. Crystallization modeling of the recalculated Dho 287A bulk‐composition yields a reasonable fit between predicted and observed mineral abundances and compositions.     

On the structure of mare basalt lava flows from textural analysis of the LaPaz Icefield and Northwest Africa 032 lunar meteorites

Abstract— Quantitative textural data for Northwest Africa (NWA) 032 and the LaPaz (LAP) mare basalt meteorites (LAP 02205, LAP 02224, LAP 02226, and LAP 02436) prvide constraints on their crystallization and mineral growth histories. In conjunction with whole‐rock and mineral chemistry, textural analysis provides powerful evidence for meteorite pairing. Petrographic observations and crystal size distribution (CSD) measurements of NWA 032 indicate a mixed population of slowly cooled phenocrysts and faster cooled matrix. LaPaz basalt crystal populations are consistent with a single phase of nucleation and growth. Spatial distribution patterns (SDP) of minerals in the meteorites highlight the importance of clumping and formation of clustered crystal frameworks in their melts, succeeded by continued nucleation and growth of crystals. This process resulted in increasingly poor sorting, during competition for growth, as the melt crystallized. Based on CSD and SDP data, we suggest a potential lava flow geometry model to explain the different crystal populations for NWA 032 and the LaPaz basalts. This model involves crystallization of early formed phenocrysts at hypabyssal depths in the lunar crust, followed by eruption and flow differentiation on the lunar surface. Lava flow differentiation would allow for formation of a cumulate base and facilitate variable cooling within the stratigraphy, explaining the varied textures and modal mineralogies of mare basalt meteorites. The model may also provide insight into the relative relationships of some Apollo mare basalt suites, shallow‐level crystal fractionation processes, and the nature of mare basalt volcanism over lunar history.     

PETROLOGICAL CHARACTER OF THE LUNA 16 SAMPLE FROM MARE FECUNDITATIS

We have classified 1858 lithic and vitreous fragments from the Luna 16 core-tube sample. They were taken from the soil fractions ranging in size from 150 to 425 μ, at levels A and G (γ). No important differences are observed between the proportions of particle types in levels A and G, nor between the soils of Luna 16 and those from the Apollo 11 landing site in the nearby Mare Tranquillitatis. Luna 16 basalts are texturally and mineralogically similar to Apollo 11 basalts, though the former are characterized by more Fe-rich olivines and pyroxenes and by lower ilmenite contents than are Apollo 11 basalts. The atomic ratio Al/Ti in Luna 16 basalt pyroxenes in about 1.5; Apollo 11 basalt pyroxenes have Al/Ti = 2.0, indicating the possibility of a lower mean valence for Ti in the Luna 16 material than in the Apollo 11 material. Most light-colored lithic fragments are anorthositic rather than noritic in character and are comparable to Apollo 11 anorthosites in mineral chemistry. We believe they are samples of terra regions to the north of the Luna 16 landing site. Triangular diagrams plotting normative plagioclase, normative mafics plus oxides, and normative orthoclase plus apatite neatly separate the three major types of lunar materials — mare basalts, anorthosites, and noritic rocks — and reveal that the Luna 16 regolith is composed of mare basalt and anorthosite, with very little norite component. Colorless-to-greenish glass occurs in the Luna 16 sample, which has high Fe and low Ti; it may represent gabbroic rock related to the anorthosites     

The early geological history of the Moon inferred from ancient lunar meteorite Miller Range 13317

Miller Range (MIL) 13317 is a heterogeneous basalt‐bearing lunar regolith breccia that provides insights into the early magmatic history of the Moon. MIL 13317 is formed from a mixture of material with clasts having an affinity to Apollo ferroan anorthosites and basaltic volcanic rocks. Noble gas data indicate that MIL 13317 was consolidated into a breccia between 2610 ± 780 Ma and 1570 ± 470 Ma where it experienced a complex near‐surface irradiation history for ~835 ± 84 Myr, at an average depth of ~30 cm. The fusion crust has an intermediate composition (Al₂O₃ 15.9 wt%; FeO 12.3 wt%) with an added incompatible trace element (Th 5.4 ppm) chemical component. Taking the fusion crust to be indicative of the bulk sample composition, this implies that MIL 13317 originated from a regolith that is associated with a mare‐highland boundary that is KREEP‐rich (i.e., K, rare earth elements, and P). A comparison of bulk chemical data from MIL 13317 with remote sensing data from the Lunar Prospector orbiter suggests that MIL 13317 likely originated from the northwest region of Oceanus Procellarum, east of Mare Nubium, or at the eastern edge of Mare Frigoris. All these potential source areas are on the near side of the Moon, indicating a close association with the Procellarum KREEP Terrane. Basalt clasts in MIL 13317 are from a very low‐Ti to low‐Ti (between 0.14 and 0.32 wt%) source region. The similar mineral fractionation trends of the different basalt clasts in the sample suggest they are comagmatic in origin. Zircon‐bearing phases and Ca‐phosphate grains in basalt clasts and matrix grains yield ²⁰⁷Pb/²⁰⁶Pb ages between 4344 ± 4 and 4333 ± 5 Ma. These ancient ²⁰⁷Pb/²⁰⁶Pb ages indicate that the meteorite has sampled a range of Pre‐Nectarian volcanic rocks that are poorly represented in the Apollo, Luna, and lunar meteorite collections. As such, MIL 13317 adds to the growing evidence that basaltic volcanic activity on the Moon started as early as ~4340 Ma, before the main period of lunar mare basalt volcanism at ~3850 Ma.     

Magnesium isotopic fractionation in chondrules from the Murchison and Murray CM2 carbonaceous chondrites

We present high‐precision measurements of the Mg isotopic compositions of a suite of types I and II chondrules separated from the Murchison and Murray CM2 carbonaceous chondrites. These chondrules are olivine‐ and pyroxene‐rich and have low ²⁷Al/²⁴Mg ratios (0.012–0.316). The Mg isotopic compositions of Murray chondrules are on average lighter (δ²⁶Mg ranging from ?0.95‰ to ?0.15‰ relative to the DSM‐3 standard) than those of Murchison (δ²⁶Mg ranging from ?1.27‰ to +0.77‰). Taken together, the CM2 chondrules exhibit a narrower range of Mg isotopic compositions than those from CV and CB chondrites studied previously. The least‐altered CM2 chondrules are on average lighter (average δ²⁶Mg = ?0.39 ± 0.30‰, 2SE) than the moderately to heavily altered CM2 chondrules (average δ²⁶Mg = ?0.11 ± 0.21‰, 2SE). The compositions of CM2 chondrules are consistent with isotopic fractionation toward heavy Mg being associated with the formation of secondary silicate phases on the CM2 parent body, but were also probably affected by volatilization and recondensation processes involved in their original formation. The low‐Al CM2 chondrules analyzed here do not exhibit any mass‐independent variations in ²⁶Mg from the decay of ²⁶Al, with the exception of two chondrules that show only small variations just outside of the analytical error. In the case of the chondrule with the highest Al/Mg ratio (a type IAB chondrule from Murchison), the lack of resolvable ²⁶Mg excess suggests that it either formed >1 Ma after calcium‐aluminum‐rich inclusions, or that its Al‐Mg isotope systematics were reset by secondary alteration processes on the CM2 chondrite parent body after the decay of ²⁶Al.     

The Cu isotopic composition of iron meteorites

Abstract– High‐precision Cu isotopic compositions have been measured for the metal phase of 29 iron meteorites from various groups and for four terrestrial standards. The data are reported as the δ⁶⁵Cu permil deviation of the ⁶⁵Cu/⁶³Cu ratio relative to the NIST SRM 976 standard. Terrestrial mantle rocks have a very narrow range of variations and scatter around zero. In contrast, iron meteorites show δ⁶⁵Cu approximately 2.3‰ variations. Different groups of iron meteorites have distinct δ⁶⁵Cu values. Nonmagmatic IAB‐IIICD iron meteorites have similar δ⁶⁵Cu (0.03 ± 0.08 and 0.12 ± 0.10, respectively), close to terrestrial values (approximately 0). The other group of nonmagmatic irons, IIE, is isotopically distinct (?0.69 ± 0.15). IVB is the iron meteorite group with the strongest elemental depletion in Cu and samples in this group are enriched in the lighter isotope (δ⁶⁵Cu down to ?2.26‰). Evaporation should have produced an enrichment in ⁶⁵Cu over ⁶³Cu (δ⁶⁵Cu >0) and can therefore be ruled out as a mechanism for volatile loss in IVB meteorites. In silicate‐bearing iron meteorites, Δ¹⁷O correlates with δ⁶⁵Cu. This correlation between nonmass‐dependent and mass‐dependent parameters suggests that the Cu isotopic composition of iron meteorites has not been modified by planetary differentiation to a large extent. Therefore, Cu isotopic ratios can be used to confirm genetic links. Cu isotopes thus confirm genetic relationships between groups of iron meteorites (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites). Several genetic connections between iron meteorites groups are confirmed by Cu isotopes, (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites).     

Petrography,mineralogy, and trace element geochemistry of lunar meteorite Dhofar 1180

Abstract— Here we report the petrography, mineralogy, and trace element geochemistry of the Dhofar 1180 lunar meteorite. Dhofar 1180 is predominantly composed of fine‐grained matrix with abundant mineral fragments and a few lithic and glassy clasts. Lithic clasts show a variety of textures including cataclastic, gabbroic, granulitic, ophitic/subophitic, and microporphyritic. Both feldspathic and mafic lithic clasts are present. Most feldspathic lithic clasts have a strong affinity to ferroan anorthositic suite rocks and one to magnesian suite rocks. Mafic lithic clasts are moderately to extremely Fe‐rich. The Ti/[Ti+Cr]‐Fe/[Fe+Mg] compositional trend of pyroxenes in mafic lithic clasts is consistent with that of low‐Ti mare basalts. Glasses display a wide chemical variation from mafic to feldspathic. Some glasses are very similar to those from Apollo 16 soils. KREEP components are essentially absent in Dhofar 1180. One glassy clast is rich in K, REE and P, but its Mg/[Mg+Fe] is very low (0.25). It is probably a last‐stage differentiation product of mare basalt. Molar Fe/Mn ratios of both olivine and pyroxene are essentially consistent with a lunar origin. Dhofar 1180 has a LREE‐enriched (La 18 × CI, Sm 14 × CI) pattern with a small positive Eu anomaly (Eu 15 × CI). Th concentration is 0.7 ppm in Dhofar 1180. Petrography, mineralogy, and trace element geochemistry of Dhofar 1180 are different from those of other lunar meteorites, indicating that Dhofar 1180 represents a unique mingled lunar breccia derived from an area on the lunar nearside but far away from the center of the Imbrium Basin.     

Isotopic composition of carbon and nitrogen in ureilitic fragments of the Almahata Sitta meteorite

This study characterizes carbon and nitrogen abundances and isotopic compositions in ureilitic fragments of Almahata Sitta. Ureilites are carbon‐rich (containing up to 7 wt% C) and were formed early in solar system history, thus the origin of carbon in ureilites has significance for the origin of solar system carbon. These samples were collected soon after they fell, so they are among the freshest ureilite samples available and were analyzed using stepped combustion mass spectrometry. They contained 1.2–2.3 wt% carbon; most showed the major carbon release at temperatures of 600–700 °C with peak values of δ¹³C from ?7.3 to +0.4‰, similar to literature values for unbrecciated (“monomict”) ureilites. They also contained a minor low temperature (≤500 °C) component (δ¹³C = ca ?25‰). Bulk nitrogen contents (9.4–27 ppm) resemble those of unbrecciated ureilites, with major releases mostly occurring at 600–750 °C. A significant lower temperature release of nitrogen occurred in all samples. Main release δ¹⁵N values of ?53 to ?94‰ fall within the range reported for diamond separates and acid residues from ureilites, and identify an isotopically primordial nitrogen component. However, they differ from common polymict ureilites which are more nitrogen‐rich and isotopically heavier. Thus, although the parent asteroid 2008TC₃ was undoubtedly a polymict ureilite breccia, this cannot be deduced from an isotopic study of individual ureilite fragments. The combined main release δ¹³C and δ¹⁵N values do not overlap the fields for carbonaceous or enstatite chondrites, suggesting that carbon in ureilites was not derived from these sources.