SPECTROSCOPY OF MARS FROM 2.04 TO 2.44 MU-M DURING THE 1993 OPPOSITION - ABSOLUTE CALIBRATION AND ATMOSPHERIC VS MINERALOGIC ORIGIN OF NARROW ABSORPTION FEATURES
Jf. Bell et al., SPECTROSCOPY OF MARS FROM 2.04 TO 2.44 MU-M DURING THE 1993 OPPOSITION - ABSOLUTE CALIBRATION AND ATMOSPHERIC VS MINERALOGIC ORIGIN OF NARROW ABSORPTION FEATURES, Icarus, 111(1), 1994, pp. 106-123
We present moderate-resolution (lambda/DELTAlambda = 300 to 370) refle
ctance spectra of Mars from 2.04 to 2.44 mum that were obtained at UKI
RT during the 1993 opposition. Seven narrow absorption features were d
etected and found to have a Mars origin. By comparison with solar and
Mars atmospheric spectra, five of these features were attributed all o
r in part to Mars atmospheric CO2 or CO (2.052 +/- 0.003, 2.114 +/- 0.
002, 2.150 +/- 0.003, 2.331 +/- 0.001, and 2.357 +/- 0.002 mum). Two o
f the bands (2.331 +/- 0.001 and 2.357 +/- 0.002 mum) appear to have w
idths and depths that are consistent with additional, nonatmospheric a
bsorptions, although a solar contribution cannot be entirely ruled out
. Two other weak bands centered at 2.278 +/- 0.002 and 2.296 +/- 0.002
mum may be at least partially mineralogic in origin. The data provide
no conclusive identification of the mineralogy responsible for these
absorption features. However, examination of terrestrial spectral libr
aries and previous moderate spectral resolution mineral studies indica
tes that the most likely origin of these features is either (bi)carbon
ate or (bi)sulfate anions in framework silicates or (Fe, Mg)-OH bonds
in sheet silicates. If the bands are caused by phyllosilicate minerals
, then an explanation must be found for the extremely narrow widths of
the cation-OH features in the Mars spectra as compared to terrestrial
minerals. (C) 1994 Academic Press, Inc.