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The effects of grain size and shape on the reflectance spectra of mineral mixtures are investigated to improve a reflectance model called the isograin model, whose prototype was proposed by M. Kinoshita in 1985. The sample powder was assumed to consist of an infinite number of layers, each of which has the same thickness with the grain size d.
Substantial progress has been made towards a better understanding of the dissolution of common gas/fluid phase components, notably H2O and CO2, in minerals. It has been shown that the dissolution mechanisms are significantly more complex than currently believed. By judiciously combining various solid state analytical techniques, convincing evidence was obtained that traces of dissolved gas/fluid phase components undergo, at least in part, a redox conversion by which they split into reduced H2 and and reduced C on one hand and oxidized oxygen, O(-), on the other. Analysis for 2 and C as well as for any organic molecules which may form during the process of co-segregation are still impeded by the omnipresent danger of extraneous contamination. However, the presence of O(-), an unusual oxidized form of oxygen, has been proven beyond a reasonable doubt. The presence of O(-) testifies to the fact that a redox reaction must have taken place in the solid state involving the dissolved traces of gas/fluid phase components. Detailed information on the techniques used and the results obtained are given.
SO2 and CO2 from pyrolysis and combustion of bulk Chassigny and infrared traces of sulfate and carbonate minerals have been previously reported. Using scanning electron microscopy (SEM) and energy-dispersive x ray spectrometry (EDS), portions of these samples are searched, and a Ca-sulfate/carbonate association is confirmed.
Iron-enriched smectites have been suggested as important mineral compounds of the Martian soil. They were shown to comply with the chemical analysis of the Martian soil, to simulate many of the findings of the Viking Labeled Release Experiments on Mars, to have spectral reflectance in the VIS-NIR strongly resembling the bright regions on Mars. The analogy with Mars soil is based, in a number of aspects, on the nature and behavior of the iron oxides and oxyhydroxides deposited on the surface of the clay particles. A summary of the properties of these iron phases and some recent findings are presented. Their potential relevance to Mars surface processes is discussed.
The 950/560-nm spectral ratio has been traditionally used as a qualitative indicator or lunar soil maturity because the 950-nm band falls within the major Fe(2+) mineral absorption bands near 1-micron characteristic of relatively immature crystalline surfaces. Since there are several other processes unrelated to maturation that may affect this ratio value, the 950/730-nm ratio has been evaluated as a potentially better measure of the relative 1-micron band strength. It is found that the 950/730-nm ratio appears to be much more sensitive to the 1-micron band depth, but it is believed that other unknown variables preclude using these single ratios to provide meaningful quantitative results at this time.
The purpose of this work was to demonstrate the feasibility of vapor-phase reduction (pyrolysis) of lunar materials to produce oxygen. Solar furnace experiments were conducted on two common lunar minerals, ilmenite and anorthite. Thermodynamic equilibrium calculations predicted that ilmenite should show a larger pressure increase than anorthite under conditions of the experiments and this was confirmed by the experiments. The measured mass loss of the ilmenite sample was consistent with loss of oxygen by reduction of iron in the liquid phase; this result was also predicted from equilibrium calculations. Based on preliminary experiments and equilibrium calculations, the temperatures needed for pyrolysis are expected to be in the range of 2000 to 2500 K, giving total gas pressures of 0.01 to 1 torr. Bulk regolith can be used as a feedstock without extensive beneficiation. Further, selective condensation of metal-containing species from the gas phase may yield metallic iron and silicon as byproducts from the process.
The formation mechanisms are described of positive holes - electronic defects in the O2 sublattice - with attention given to detecting the positive surface charge of minerals with these holes. Charge distribution analysis (CDA) is presented which measures dielectric polarization in an inhomogeneous field. CDA can be applied to the detection of the peroxide/superoxide functionality caused by positive holes on the surface. It is demonstrated with obsidian that the measurements provide data on O(-) mobility as a function of surface-charge carrier density and on O(-) generation as a function of temperature.
The solubilities of Ne, Ar, Kr, and Xe gases were measured in natural samples of anorthite, diopside, forsterite, spinel, and synthetic basaltic melts, the samples which represent equilibrium pairs in the Fo-An-Di-SiO2 system. Results show that, in natural minerals, the solubilities of these gases increase with increasing atomic number. In contrast, the solubilities of noble gases in the synthetic basaltic melts decreased with increasing atomic number. The partition coefficients increased with increasing atomic number for all mineral/melt pairs.
Algorithms were developed, based on Hapke's (1981) equations, for remote determinations of mineral abundances and particle sizes from reflectance spectra. In this method, spectra are modeled as a function of end-member abundances and illumination/viewing geometry. The method was tested on a laboratory data set. It is emphasized that, although there exist more sophisticated models, the present algorithms are particularly suited for remotely sensed data, where little opportunity exists to independently measure reflectance versus article size and phase function.
The first high-resolution quantitative directional hemispherical reflectance spectra of minerals were obtained for different particle sizes, and were used to develop an accurate prediction of the particles' spectral emissivity, using Kirchhoff's law (Nicodemus, 1965) and to interpret the nature and causes of changes in the spectral contrast of reststrahlen bands. It was found that the reststrahlen bands change in shape as well as intensity; this is explained by the occurrence of substantial volume scattering at fine particle sizes. The implication of this finding for remote sensing of the earth, moon, Mercury, Mars, and the asteroids is discussed.
Thermal Analyzer for Planetary Soil (TAPS) offers a specific implementation for the generic thermal analyzer/evolved-gas analyzer (TA/EGA) function included in the Mars Environmental Survey (MESUR) strawman payload; applications to asteroids and comets are also possible. The baseline TAPS is a single-sample differential scanning calorimeter (DSC), backed by a capacitive-polymer humidity sensor, with an integrated sampling mechanism. After placement on a planetary surface, TAPS acquires 10-50 mg of soil or sediment and heats the sample from ambient temperature to 1000-1300 K. During heating, DSC data are taken for the solid and evolved gases are swept past the water sensor. Through ground based data analysis, multicomponent DSC data are deconvolved and correlated with the water release profile to quantitatively determine the types and relative proportions of volatile-bearing minerals such as clays and other hydrates, carbonates, and nitrates. The rapid-response humidity sensors also achieve quantitative analysis of total water. After conclusion of soil-analysis operations, the humidity sensors become available for meteorology. The baseline design fits within a circular-cylindrical volume less than 1000 cm(sup 3), occupies 1.2 kg mass, and consumes about 2 Whr of power per analysis. Enhanced designs would acquire and analyze multiple samples and employ additional microchemical sensors for analysis of CO2, SO2, NO(x), and other gaseous species. Atmospheric pumps are also being considered as alternatives to pressurized purge gas.
Perhaps the most conspicuous indication that chemical weathering has occurred on the surface of Mars is the overall color of the red planet and the spectroscopic features that identify ferric-bearing assemblages in the martian regolith. Apparently, Fe(2+) ions in primary minerals in parent igneous rocks on the martian surface have been oxidized to ferric iron, which occurs in degradation products that now constitute the regolith. The mineralogy of the unweathered igneous rocks prior to weathering on the martian surface is reasonably well constrained, mainly as a result of petrographic studies of the SNC meteorites. However, the alteration products resulting from oxidative weathering of these rocks are less well-constrained. The topics covered include the following: primary rocks subjected to chemical weathering; dissolution processes; oxidation of dissolved Fe(2+); mechanism of polymerization of hydrous ferric oxides; terrestrial occurrences of ferromagnesian smectites; and dehydroxylated Mg-Fe smectites on Mars.
Previously, the effect of weathering a basalt of Shergotty meteorite composition with pure water buffered at martian atmospheric values of CO2 and O2, to place constraints upon the composition of martian groundwater, and to determine possible equilibrium mineral assemblages was calculated. A revised calculation of the composition of the aqueous phase in the weathering reaction as a function of the amount of basalt titrated into the solution is shown. The concentrations of sulfate and chloride ions increase in the solution from high water/rock ratios (w/r) on the left to low water/rock ratios on the right, until at w/r = 1, where 1 kg of basalt has been titrated, sulfate concentration is 1564 ppm and chloride is 104 ppm. This resulting fluid is dominated by sulfate and sodium, with bicarbonate and chloride at about the same concentration. This solution was evaporated in an attempt to determine if the resulting evaporite can explain the Viking XRF data. The program CHILLER was used to evaporate this solution at 0.1 C.
The comminution behavior of different mineral species subjected to incessant impact is investigated using targets consisting of 2-4-mm crystals of albite, augite, forsterite, of quartz, which were impacted at least 25 times at 1.4 km/sec by 3.18-mm stainless-steel spheres. Sieve analyses were performed after every five shots. It was found that the behaviors of the feldspar and quartz were virtually indistinguishable and that the olivine target produced the greatest proportion of fines. The pyroxene target was most resistant to comminution. The comminution was only mildly dependent on grain size.
The feasibility of using imaging spectrometry in studies of playa evaporites is demonstrated by mapping efflorescent salt crusts in Death Valley (California), using Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data and a recently developed least-squares spectral band-fitting algorithm. It is shown that it was possible to remotely identify eight different saline minerals, including three borates that have not been previously reported for the Death Valley efflorescent crusts: hydroboracite, pinnoite, and rivadavite. The three borates are locally important phases in the crusts; at least one of them, rivadavite, appears to be forming directly from brine.
Maturity, which is a measure of the time lunar soils have been in the upper approximately 1 mm of the surface, is correlated with changes in the soils' optical properties. Mature soil is darker and somewhat redder than immature soil of the same composition, and features in the reflectance spectrum become more subdued with increasing maturity. The maturation process also involves accumulation of agglutinitic glass and submicroscopic metallic iron particles. We have produced submicrometer iron metal blebs on the surface and within glass and mineral grains by the method of high-temperature reduction. This technique has permitted the determination of optical changes in samples much simpler than lunar soil, and offers a useful tool with which to investigate the maturation process.
Spectral evidence from Viking and Phobos orbiting spacecraft suggests the local development of crystalline ferric oxides in a small region within Mars' equatorial Valles Marineris canyon system. This is the same area noted for its anomalous coloration in Viking Orbiter image 583 A by McEwen. The unique hue of the region in Viking color data is due to a reduced green filter reflectance, relative to violet and red, in comparison to surrounding materials of similar albedo or average reflectance. For this reason, the region does not appear spectrally distinctive in later Survey Mission images which were acquired without the green filter. In high resolution, the spectral unit can be seen to correspond to two 20 km long depressions on the margins of Candor Mensa, a heavily eroded plateau-forming deposit on the canyon floor. Laminae are conspicuous in several places on the plateau, particularly where 15 to 20 cycles of alternating bright and dark laminae are exposed at approximately 200 meter vertical intervals. Laminae are also visible on the steep, vertically fluted cliffs to the south of this depression. Concentric laminae indicate a basis in the depression on the southeastern margin of Candor Mensa at the location of the less pronounced hue anomaly. A distinct lineation at the base of the scarp at the western end of the canyon transects mottled canyon floor deposits believed to be among the youngest in the Valles marineris. Water is implicated in the formation of the iron oxides, since the steep surfaces of layered sediments elsewhere on Candor Mensa show no evidence of unusual coloration despite the fact that these materials were deposited concurrently with the strata exposed in the depressions. This suggests that the mineralization is secondary in nature and developed locally in association with the depressions, which could have ponded surface runoff or groundwater seepage.
Many current models for the origin of lunar highland rocks feature as an essential component the assimilation of KREEPy material by primitive magmas parental to the Mg-rich suite and alkali suite plutonic rocks. Similar models have also been proposed for the origin of various mare basalt suites. However, any model which considers assimilation of KREEP an important petrologic process must sooner-or-later deal with the question: what is KREEP? Because pristine KREEP basalts are rare, and most known samples are small (e.g., 15382/15386), the geochemical variability of KREEP basalts is poorly known. Other KREEP compositions which are commonly used in these models include the hypothetical 'high-K KREEP' component of Warren and Wasson, which is derived from Apollo 14 soil data, and the 'superKREEP' quartz-monzodiorite 15405. Lunar breccia 15205 is a polymict regolith breccia that consists of approximately 20% KREEP basalt clasts and 20% quartz-normative basalt clasts in a KREEP-rich matrix. Bulk rock mixing calculations show that this sample comprises about 84% KREEP. The clasts range up to 1 cm in size, but most are considerably smaller. The primary aim is to characterize pristine KREEP basalts petrographically, to establish the range in chemical compositions of KREEP basalts, and to test models that were proposed for their origin. In addition, we may be able to extend the compositional range recognized in the quartz-normative basalt suite and cast some light on its origin as well. Preliminary whole rock geochemical data on the KREEP basalts are presented in a companion paper by M.M. Lindstrom and co-workers. Concentration is on petrography and mineral chemistry of these clasts, and the implications these data have for the origin of the different melt rock suites.