Wanted: Lunar detectives to unravel the mysteries of the Moon! Crime to be solved: Mass extinctions on the Moon by meteorite impact!

The criteria and clues for identifying meteorite contamination are outlined to aid in the quest for more knowledge regarding the evolution of the Moon and the early Earth. The Warren and Wasson seven criteria for establishing the pristine nature of highland rocks are presented. Other topics covered include iron/nickel metals, monomict nature, and lunar glasses. The major conclusion is that pristinity should not be the primary consideration in the study of lunar rocks. The most important criterion to establish is whether or not the lunar sample contains more than one lunar rock type. Even if a sample is non-pristine, as long as only one lunar rock type is present, petrogenetic interpretation can still be carried out

The Apollo 17 mare basalts: Serenely sampling Taurus-Littrow

As we are all aware, the Apollo 17 mission marked the final manned lunar landing of the Apollo program. The lunar module (LM) landed approximately 0.7 km due east of Camelot Crater in the Taurus-Littrow region on the southwestern edge of Mare Serenitatis. Three extravehicular activities (EVA's) were performed, the first concentrating around the LM and including station 1 approximately 1.1 km south-southeast of the LM at the northwestern edge of Steno Crater. The second traversed approximately 8 km west of the LM to include stations 2, 3, 4, and 5, and the third EVA traversed approximately 4.5 km to the northwest of the LM to include stations 6, 7, 8, and 9. This final manned mission returned the largest quantity of lunar rock samples, 110.5 kg/243.7 lb, and included soils, breccias, highland samples, and mare basalts. This abstract concentrates upon the Apollo 17 mare basalt samples

Using Apollo 17 high-Ti mare basalts as windows to the lunar mantle

The Apollo 17 high-Ti mare basalts are derived from source regions containing plagioclase that was not retained in the residue. Ilmenite appears to remain as a residual phase, but plagioclase is exhausted. The open-system behavior of the type B2 basalts results in slightly higher Yb/Hf and La/Sm ratios. The nature of the added component is not clear, but may be a KREEP derivative or residue. The recognition of plagioclase in the source(s) of these basalts suggests that the location of the source region(s) would be more likely to be less than 150 km (i.e., closer to the plagioclase-rich crust), which would allow incorporation of plagioclase into the source through incomplete separation of crustal feldspar

Evidence for a "Wet" Early Moon

The Moon was thought to have lost its volatiles during impact(s) of a Mars-size planetesimal with the proto Earth [1] and during degassing of an early planet-wide magma ocean [2]. This view of an anhydrous Moon, however, has been challenged by recent discoveries of water on its surface [3-5] and in lunar volcanics [6-10] and regoliths [11]. Indigenous water is suggested to be heterogeneously distributed in the lunar interior and some parts of lunar mantle may contain as much water as Earth's upper mantle [6,10]. This water is thought to have been brought in part through solar wind implantation [3-5,8,11] and meteorite/cometary impacts [3,4,8,12] after the formation of the primary crust. Here we measured water in primary products of the Lunar Magma Ocean (LMO) thereby by-passing the processes of later addition of water to the Moon through impact events or during mantle overturn as suggested by previous studies (e.g., [8,12]). So far, ferroan anorthosite (FAN) is the only available lithology that is believed to be a primary product of the LMO [2]. It is generally accepted that plagioclase, after crystallization, floated in the LMO and formed FAN as the original crust [2]. Therefore, any indigenous water preserved in FAN was partitioned from the LMO. These data can be used to estimate the water content of the magma ocean at the time of plagioclase crystallization, as well as that of the mare magma source regions

Derivation of Apollo 14 High-Al Basalts at Discrete Times: Rb-Sr Isotopic Constraints

Pristine Apollo 14 (A-14) high-Al basalts represent the oldest volcanic deposits returned from the Moon [1,2] and are relatively enriched in Al2O3 (>11 wt%) compared to other mare basalts (7-11 wt%). Literature Rb-Sr isotopic data suggest there are at least three different eruption episodes for the A-14 high-Al basalts spanning the age range approx.4.3 Ga to approx.3.95 Ga [1,3]. Therefore, the high-Al basalts may record lunar mantle evolution between the formation of lunar crust (approx.4.4 Ga) and the main basin-filling mare volcanism (<3.85 Ga) [4]. The high-Al basalts were originally classified into five compositional groups [5,6], and then regrouped into three with a possible fourth comprising 14072 based on the whole-rock incompatible trace element (ITE) ratios and Rb-Sr radiometric ages [7]. However, Rb-Sr ages of these basalts from different laboratories may not be consistent with each other because of the use of different 87Rb decay constants [8] and different isochron derivation methods over the last four decades. This study involved a literature search for Rb-Sr isotopic data previously reported for the high-Al basalts. With the re-calculated Rb-Sr radiometric ages, eruption episodes of A-14 high-Al basalts were determined, and their petrogenesis was investigated in light of the "new" Rb-Sr isotopic data and published trace element abundances of these basalts

Exploring the Moon's surface for remnants of the lunar mantle 1. Dunite xenoliths in mare basalts. A crustal or mantle origin?

Remotely sensed observations from recent missions (e.g., GRAIL, Kaguya, Chandrayaan-1) have been interpreted as indicating that the deep crust and upper mantle are close to or at the lunar surface in many large impact basins (e.g., Crisium, Apollo, Moscoviense). If this is correct, the capability of either impact or volcanic processes to transport mantle lithologies to the lunar surface should be enhanced in these regions. Somewhat problematic to these observations and interpretations is that examples of mantle lithologies in the lunar sample collection (Apollo Program, Luna Program, lunar meteorites) are at best ambiguous. Dunite xenoliths in high-Ti mare basalt 74275 are one of these ambiguous examples. In this high-Ti mare basalt, olivine occurs in three generations: olivine associated with dunite xenoliths, olivine megacrysts, and olivine microphenocrysts. The dunite xenoliths are anhedral in shape and are generally greater than 800 μm in diameter. The interior of the xenoliths are fairly homogeneous with regard to many divalent cations. For example, the Mg# (Mg/Mg + Fe × 100) ranges from 82 to 83 in their interiors and decreases from 82 to 68 over the 10–30 μm wide outer rim. Titanium and phosphorus X-ray maps of the xenolith illustrate that these slow diffusing elements preserve primary cumulate zoning textures. These textures indicate that the xenoliths consist of many individual olivine grains approximately 150–200 μm in diameter with low Ti, Al, and P cores. These highly incompatible elements are enriched in the outer Fe-rich rims of the xenoliths and slightly enriched in the rims of the individual olivine grains. Highly compatible elements in olivine such as Ni exhibit a decrease in the rim surrounding the xenolith, an increase in the incompatible element depleted cores of the individual olivine grains, and a slight decrease in the “interior rims” of the individual olivine grains. Inferred melt composition, liquid lines of descent, and zoning profiles enable the reconstruction of the petrogenesis of the dunite xenoliths. Preservation of primary magmatic zoning (Ti, P, Al) and lack of textures similar to high-pressure mineral assemblages exhibited by the Mg-suite (Shearer et al. 2015) indicate that these xenoliths do not represent deep crustal or shallow mantle lithologies. Further, they are chemically and mineralogically distinct from Mg-suite dunites identified from the Apollo 17 site. More likely, they represent olivine cumulates that crystallized from a low-Ti mare basalt at intermediate to shallow crustal levels. The parent basalt to the dunite xenolith lithology was more primitive than low-Ti basalts thus far returned from the Moon. Furthermore, this parental magma and its more evolved daughter magmas are not represented in the basalt sample suite returned from the Taurus-Littrow Valley by the Apollo 17 mission. The dunite xenolith records several episodes of crystallization and re-equilibration. During the last episode of re-equilibration, the dunite cumulate was sampled by the 74275 high-Ti basalt and transported over a period of 30–70 days to the lunar surface

Sims Analysis of Water Abundance and Hydrogen Isotope in Lunar Highland Plagioclase

The detection of indigenous water in mare basaltic glass beads has challenged the view established since the Apollo era of a "dry" Moon. Since this discovery, measurements of water in lunar apatite, olivine-hosted melt inclusions, agglutinates, and nominally anhydrous minerals have confirmed that lunar igneous materials contain water, implying that some parts of lunar mantle may have as much water as Earth's upper mantle. The interpretation of hydrogen (H) isotopes in lunar samples, however, is controversial. The large variation of H isotope ratios in lunar apatite (delta Deuterium = -202 to +1010 per mille) has been taken as evidence that water in the lunar interior comes from the lunar mantle, solar wind protons, and/or comets. The very low deuterium/H ratios in lunar agglutinates indicate that solar wind protons have contributed to their hydrogen content. Conversely, H isotopes in lunar volcanic glass beads and olivine-hosted melt inclusions being similar to those of common terrestrial igneous rocks, suggest a common origin for water in both Earth and Moon. Lunar water could be inherited from carbonaceous chondrites, consistent with the model of late accretion of chondrite-type materials to the Moon as proposed by. One complication about the sources of lunar water, is that geologic processes (e.g., late accretion and magmatic degassing) may have modified the H isotope signatures of lunar materials. Recent FTIR analyses have shown that plagioclases in lunar ferroan anorthosite contain approximately 6 ppm H2O. So far, ferroan anorthosite is the only available lithology that is believed to be a primary product of the lunar magma ocean (LMO). A possible consequence is that the LMO could have contained up to approximately 320 ppm H2O. Here we examine the possible sources of water in the LMO through measurements of water abundances and H isotopes in plagioclase of two ferroan anorthosites and one troctolite from lunar highlands

A heterogeneous lunar interior for hydrogen isotopes as revealed by the lunar highlands samples

Knowing the amount and timing of water incorporation into the Moon has fundamental implications for our understanding of how the Earth–Moon system formed. Water has been detected in lunar samples but its abundance, distribution and origin are debated. To address these issues, we report water concentrations and hydrogen isotope ratios obtained by secondary ion mass spectrometry (SIMS) of plagioclase from ferroan anorthosites (FANs), the only available lithology thought to have crystallized directly from the lunar magma ocean (LMO). The measured water contents are consistent with previous results by Fourier transform infrared spectroscopy (FTIR). Combined with literature data, δD values of lunar igneous materials least-degassed at the time of their crystallization range from −280 to +310‰, the latter value being that of FAN 60015 corrected for cosmic ray exposure. We interpret these results as hydrogen isotopes being fractionated during degassing of molecular hydrogen (H_2) in the LMO, starting with the magmatic δD value of primordial water at the beginning of LMO being about −280‰, evolving to about +310‰ at the time of anorthite crystallization, i.e. during the formation of the primary lunar crust. The degassing of hydrogen in the LMO is consistent with those of other volatile elements. The wide range of δD values observed in lunar igneous rocks could be due to either various degrees of mixing of the different mantle end members, or from a range of mantle sources that were degassed to different degrees during magma evolution. Degassing of the LMO is a viable mechanism that resulted in a heterogeneous lunar interior for hydrogen isotopes

A strontium and neodymium isotopic study of Apollo 17 high-Ti mare basalts: Resolution of ages, evolution of magmas, and origins of source heterogeneities

A combined Sr and Nd isotopic study of 15 Apollo 17 high-Ti mare basalts was undertaken to investigate geochronological and compositional differences between previously identified magma types (A, B1, B2, and C). Whole-rock and mineral separates for one of the least-evolved Type B1 basalts, 70139, yield Sm-Nd and Rb-Sr isochron ages of 3.71 +/- 0.12 Ga and 3.65 +/- 0.13 Ga, respectively. A more-evolved, Type A basalt, 71539, exhibits a slightly older Sm-Nd isochron age of 3.75 +/- 0.07 Ga and a Rb-Sr isochron age of 3.67 +/-0.10 Ga. Although these two ages are non-resolvable by themselves, compilation of all available geochronological data allows resolution of Type A and B1/B2 ages at high levels of confidence (&gt;99%). The most reliably dated samples, classified according to their geochemical type, yield weighted average ages of 3.75 +/- 0.02 Ga for Type A (N = 4) and 3.69 +/- 0.02 Ga for Type B1/B2 (N = 3) basalts. Insufficient geochronological data are available to place the rare, Type C basalts within this stratigraphy. We propose that age differences correlate with geochemical magma type, and that early magmatism was dominated by eruption of Type A basalts while later activity was dominated by effusion of Type B1 and B2 basalts.Whole-rock isotopic data yield distinct differences in initial Sr and Nd isotopic compositions between Types A, B1, B2, and C basalts. Types A, B1, and C exhibit restricted intra-group compositional variations and lie along well-defined whole-rock isochrons. These data are consistent with petrogenetic models involving closed-system fractionation of observed microphenocrysts from chemically and isotopically distinct parental magmas. In contrast, a wide range of Type B2 initial isotopic compositions indicates mixing of several distinct components during magma evolution.The Sm-Nd whole-rock isochron age for Type A, Bl, and C basalts of 3.79 +/- 0.15 Ga is within error of Apollo 17 eruptive activity. However, the very well-defined Sr whole-rock isochron age of 4.02 +/- 0.05 Ga is 270 to 330 Ma older than eruptive ages. Isotopic and petrological arguments indicate that extensive Rb/Sr fractionation did not occur at the time of melt generation. Therefore, the 4.0 Ga Sr whole-rock isochron age records a significant event at which time geochemical heterogeneities were established within the originally homogeneous basalt source regions. Types A and C sources were enriched in Rb/Sr, with little or no concurrent modification of 87Sr/86Sr, Sm/Nd, or 143Nd/144Nd. Infiltration of similar-aged KREEP magmas into mantle cumulate sources cannot explain both Sr and Nd isotopic data. Instead, we suggest a metasomatic origin in which Rb, transported as a chloride complex in halogen-rich fluids, was preferentially mobilized relative to Sr and the REEs.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/29272/1/0000331.pd