Abstract

Spurred by the discovery of water in lunar volcanic glasses about a decade ago, the accessory mineral apatite became the primary target to investigate the abundance and source of lunar water. This is due to its ability to contain significant amounts of OH in its structure, along with the widespread presence of apatite in lunar rocks. There is a general understanding that crustal cumulate rocks of the lunar magnesian (Mg) suite are better candidates for recording the original isotopic compositions of volatile elements in their parental melts compared to eruptive rocks, such as mare basalts. Consequently, water-bearing minerals in Mg-suite rocks are thought to be ideal candidates for discerning the primary hydrogen isotopic composition of water in the lunar interior. Mg-suite rocks and most other Apollo samples that were collected at the lunar surface display variable degrees of shock-deformation. In this study, we have investigated seven Apollo 17 Mg-suite samples that include troctolite, gabbro and norite lithologies, in order to understand if shock processes affected the water abundances and/or H isotopic composition of apatite. The measured water contents in apatite grains range from 31 to 964 ppm, with associated δD values varying between −535 ± 134‰ and +147 ± 194‰ (2σ). Considering the full dataset, there appears to be no correlation between H2O and δD of apatite and the level of shock each apatite grain has experienced. However, the lowest δD was recorded by individual, water-poor (<∼100 ppm H2O) apatite grains that are either directly in contact with an impact melt or in its proximity. Therefore, the low-δD signature of apatite could be a result of interactions with D-poor regolith (solar wind derived H), facilitated by shock-induced nanostructures that could have provided pathways for migration of volatiles. In contrast, in relatively water-rich apatites (>∼100 ppm H2O), regardless of the complexity of the shock-induced nanostructures, there appears to be no evidence of water-loss or alteration in their δD. The weighted average δD value of 24 such water-rich apatites is −192 ± 71‰, and, of all 36 analyzed spots is −209 ± 47‰, indistinguishable from that of other KREEPy lunar lithologies or the Earth's deep mantle. Despite experiencing variable degrees of shock-deformation at a later stage in lunar history, water-rich apatite in some of the earliest-formed lunar crustal material appears to retain the original isotopic signature of H in the Moon.

Highlights

  • The phosphate mineral apatite [Ca5(PO4)3(F,Cl,OH)] is one of the most versatile minerals found in various rocks and meteorites (Hughes, 2015)

  • Following the criteria used in Cernok et al (2019), we assess the extent of shock-deformation stages in all other primary apatite grains in samples 76255 and 73235 based upon nanostructural data presented in Supplementary Fig. 1

  • The criteria used include the extent of subgrain size, their density and total misorientation across the grain surface, which is a useful measure of crystal-plastic deformation (CPD)

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Summary

Introduction

The phosphate mineral apatite [Ca5(PO4)3(F,Cl,OH)] is one of the most versatile minerals found in various rocks and meteorites (Hughes, 2015). Water was looked for, and confirmed, in other host phases, too, for example within anorthosite (Hui et al, 2017, 2013), surface regolith (Liu et al, 2012; Stephant and Robert, 2014), melt inclusions (Hauri et al, 2011; Chen et al, 2015; Ni et al, 2019, 2017; Singer et al, 2017) and volcanic glasses (Füri et al, 2014; Saal et al, 2013) These findings necessitated a re-evaluation of the “bone-dry” Moon paradigm, established in the early 1970s, heralding a new era in our quest for understanding the history of water in the lunar interior

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