Dl. Blaney et Tb. Mccord, INDICATIONS OF SULFATE MINERALS IN THE MARTIAN SOIL FROM EARTHBASED SPECTROSCOPY, J GEO R-PLA, 100(E7), 1995, pp. 14433-14441
Telescopic measurements of Mars between 4.40 and 5.13 mu m at a spectr
al resolution (lambda/Delta lambda) of 300 were made on August 19, 198
8, UT at the NASA infrared Telescope Facility on Mauna Kea, Hawaii. Th
is wavelength region contains radiation from both solar reflection and
thermal emission. Additionally, the Martian atmosphere has numerous a
tmospheric gas absorption features, dominated by the 4.2-mu m CO2 fund
amental band. The Mars spectrum rise out of the 4.2 to 4.4-mu m CO2 ba
nd on the long-wavelength side cannot be matched solely by atmospheric
gas constituents. An absorption must be added at roughly 4.5 mu m in
order to decrease the reflectance rise and produce the 4.5-mu m inflec
tion which is present in the data. The location of this feature at the
position of the 2 nu 3 overtone of the SO42- anion indicates that the
surface absorption is probably caused by sulfates on the Martian surf
ace and/or in atmospheric dust, This is consistent with the known pres
ence of sulfates on the Martian surface from the Viking results. An ex
act spectral match to a terrestrial sulfur mineral has not been made,
but we suggest that the mineral on Mars has very weak band structure,
probably due to an ion environment in the mineral with a high degree o
f electric field symmetry. Significant variation exists at 4.5 mu m am
ong the observed spectra for different locations on Mars. In order of
strength, from strongest absorption to weakest, are Eastern Solis Plan
um, Argyre Basin, Eastern Tharsis, and Valles Marineris for the four r
egions measured at similar Mars atmospheric conditions.