COORDINATED MICROANALYSIS OF THE CHEMICAL COMPOSITION, MICROSTRUCTURE, AND VOLATILE INVENTORY OF APATITE IN HIGH-TI MARE BASALTS FROM THE MOON
Backscattered electron images of apatite in high-Ti mare basalts indicate chemical zoning. Qualitative energy dispersive spectroscopic (EDS) analysis indicates that the zonation is represented by core-to-rim variations in SiO2 and rare earth element abundances, which make up a coupled substitution in apatite for P2O5 and Ca, respectively. We also note that in high-K, high-Ti basalts apatite commonly contains thin, vein-like features that could represent an exsolved component, although the veins were too fine-scale (< 1µm) to be chemically characterized by scanning electron microscopy (SEM). Furthermore, nano-scale secondary ion mass spectrometry (NanoSIMS) analyses of apatite crystals in high-K, high-Ti basalt 10024 display fractionated δ37Cl values (~+8 to +16 ‰, relative to SMOC) and Cl contents up to ~5000 ppm. Overall, the isotopic compositions obtained agree with our analyses of other high- and low-K, high-Ti lunar basalts, which deviate from the overall δ37ClApatite-bulk rock trace element trend defined by low-Ti basalts, including KREEP basalts, from the Moon.
Here we present the results of our analyses of apatite crystals from two high-Ti mare basalts by coordinated SEM, focused ion beam (FIB), transmission electron microscopy (TEM), and NanoSIMS. The goal of this work is to fully document the chemical composition, crystal structure, and volatile abundances (F, Cl, OH, including Cl isotopes) of apatite in order to understand their history of formation and origin of volatiles. A zoned apatite from 10029 (low-K, high-Ti) and an apatite with exsolution features from 10024 were selected for coordinated analysis. To date, we have performed preliminary documentation by SEM and have taken FIB sections for analysis in the TEM. We will present results quantifying the chemical composition and crystal structure of zoned lunar apatite and exsolution features at the meeting.