HR: 14:00h
AN: U13C-02 [Abstracts]
TI: Volatiles in the Lunar Volcanic Glasses, Evidence for the Presence of Indigenous Water in the
Moon's Interior
AU: * Saal, A E
EM: asaal@brown.edu
AF: Department of Geological Sciences, Brown University, 324 Brook St., Providence, RI 02912,
United States
AU: Hauri, E H
EM: hauri@dtm.ciw.edu
AF: DTM, Carnegie Institution of Washington, 5241 Broad Branch Road, NW Washington, DC
20015, United States
AU: Lo Cascio, M
EM: Mauro_Lo_Cascio@brown.edu
AF: Department of Geological Sciences, Brown University, 324 Brook St., Providence, RI 02912,
United States
AU: Van Orman, J
EM: jav12@pop.cwru.edu
AF: Department of Geological Sciences, Case Western Reserve University, 10900 Euclid
Avenue, Cleveland, OH 44106, United States
AU: Rutherford, M
EM: malcolm_rutherford@brown.edu
AF: Department of Geological Sciences, Brown University, 324 Brook St., Providence, RI 02912,
United States
AU: Cooper, R
EM: reid_cooper@brown.edu
AF: Department of Geological Sciences, Brown University, 324 Brook St., Providence, RI 02912,
United States
AB:
The composition and origin of the lunar volatiles has been the subject of considerable interest and one of the
most important unsolved questions regarding the formation of the Moon. Volatiles influence mantle melting,
magma crystallization and volcanic eruption, and their abundances and spatial distribution provide important
constraints on models for the thermal and chemical evolution of the Moon's interior. The general consensus
today is that the Moon formed and evolved through a single or series of catastrophic heating events in which most
of the highly volatile elements were either stripped or evaporated away. Hydrogen being the lightest element is
thought to have been completely lost during this period. Most of the geochemical inferences about the deepest
section of the moon have been based on studies of the most primitive melts erupted on the Moon's surface, the
lunar volcanic glasses. We reported new volatile contents (CO2, H2O, F, S, Cl) for the lunar volcanic
glasses, which by virtue of SIMS analysis provide improved detection limits by almost an order of magnitude. All
volcanic glasses have CO2 below or within the 2 standard deviation of the detection limit for our runs (6 ppm
CO2) and will not be considered further. The volatile contents after background correction have the following
ranges: 4-46 ppm (±2 ppm 2σ) for H2O; 4-40 ppm (±0.2 ppm 2σ) for F; 115-576
ppm (±3 ppm 2σ) for S; and 0.06-2 ppm (±0.03 ppm 2σ) for Cl. Two outstanding
features of the data is the significant correlation among H2O, Cl, F and S contents, and the clear relationship
between the volatile and the major and trace element contents of the glasses. Most importantly, the correlations
among the volatiles suggest that the measured H2O content in the volcanic glasses is indigenous. To test
this hypothesis we determined concentration profiles for the volatiles within a single selected glass bead. Our
data define concentration profiles with decreasing volatile contents from the core to the rim of the glass bead.
This is especially significant for H2O, which decreases from ~30 ppm in the center to ~14 ppm in
the margin of the bead, supporting the hypothesis of the indigenous origin of H2O subsequently affected by
degassing processes during melt decompression and eruption. To our knowledge this is the first definitive
confirmation of the presence of indigenous H2O in primitive lunar basalts. Our results suggest that, contrary
to the prevailing ideas, the bulk Moon is not uniformly depleted in highly volatile elements, and the presence of
water in particular must be included to constrain models for the thermal and chemical evolution of the Moon's
interior.
DE: 1026 Composition of the moon
SC: Union [U]
MN: 2007 Fall Meeting