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At least 1,099 records · Page 61
All sourcesNASA NTRSDOE OSTI
NASA NTRS1985

Mare basalt genesis - Modeling trace elements and isotopic ratios

Various types of mare basalt data have been synthesized, leading to the production of an internally consistent model of the mare basalt source region and mare basalt genesis. The model accounts for the mineralogical, major oxide, compatible siderophile trace element, incompatible trace element, and isotopic characteristics of most of the mare basalt units and of all the pyroclastic glass units for which reliable data are available. Initial tests of the model show that it also reproduces the mineralogy and incompatible trace element characteristics of the complementary highland anorthosite suite of rocks and, in a general way, those of the lunar granite suite of rocks.

Binder, A. B.↗
NASA NTRS1986

Atmospheric-water absorption features near 2.2 micrometers and their importance in high spectral resolution remote sensing

Selective absorption of electromagnetic radiation by atmospheric gases and water vapor is an accepted fact in terrestrial remote sensing. Until recently, only a general knowledge of atmospheric effects was required for analysis of remote sensing data; however, with the advent of high spectral resolution imaging devices, detailed knowledge of atmospheric absorption bands has become increasingly important for accurate analysis. Detailed study of high spectral resolution aircraft data at the U.S. Geological Survey has disclosed narrow absorption features centered at approximately 2.17 and 2.20 micrometers not caused by surface mineralogy. Published atmospheric transmission spectra and atmospheric spectra derived using the LOWTRAN-5 computer model indicate that these absorption features are probably water vapor. Spectral modeling indicates that the effects of atmospheric absorption in this region are most pronounced in spectrally flat materials with only weak absorption bands. Without correction and detailed knowledge of the atmospheric effects, accurate mapping of surface mineralogy (particularly at low mineral concentrations) is not possible.

Kruse, F. A.↗
NASA NTRS1986

The physical basis for spectral variations in thermal infrared emittance of silicates and application to remote sensing

The use of infrared spectroscopy for the remote characterization of planetary surfaces has received attention due to efforts in the investigation of these bodies from space. In the 8 to 14 micron region, a depression in the emittance spectra of rocks (sometimes called reststrahlen) is related to the fundamental stretching vibrations of Si-O bonds and shifts in the locations of this feature are ascribed to variations in rock composition. Thus, it should be possible to investigate, quantify, and model the relationships of reststrahlen spectral band location through silicate mineralogical composition to rock classification. This concept will be tested first through the use of laboratory-acquired data on the infrared spectra and mineralogy of selected mineral and rock samples. As a suitable classification model is developed, it will be tested through overflights of appropriate rock outcrops using the Thermal Infrared Multispectral Scanner (TIMS).

Walter, Louis S.↗
NASA NTRS1987

Evolution of the inner asteroid belt: Paradigms and paradoxes from spectral studies

Recent years have witnessed a significant increase in the sophistication of asteroidal surface material characterizations derived from spectral data. An extensive data base of moderate to high spectral resolution, visible and near-infrared asteroid spectra is now available. Interpretive methodologies and calibrations were developed to determine phase abundance and composition in olivine-pyroxene assemblages and to estimate NiFe metal abundance from such spectra. A modified version of the asteroid classifications system more closely parallels the mineralogic variations of the major inner belt asteroid types. These improvements permit several general conclusions to be drawn concerning the nature of inner belt objects; their history, and that of the inner solar system; and the relationship between the asteroids and meteorites. Essentially all large belt asteroids have or are fragments of parent bodies which have undergone strong post-accretionary heating, varying degrees of melting and magmatic differentiation, and subsequent collisional disruption. These asteroids show a systematic, but not yet well characterized, mineralogic variation with semi-major axis. This suggests that the S-type asteroid families represent relatively recent collisions onto the cores of previously disrupted parent bodies.

Gaffey, Michael J.↗
NASA NTRS1987

The spectroscopic chemical and photophysical properties of Martian soils and their analogs

The program of research outlined should advance significantly the understanding of the spectral signal of montmorillonites in general and the variations produced in it by structural and surface ferric and ferrous iron and interlayer water as a function of several environmental conditions that are different between Earth and Mars. In addition, an extensive data base was collected providing spectral characterization of several features (iron, both surface and structural, OH-groups, both structural and from adsorbed water and O(-) centers) that are known, or thought to be, influential in directing the surface activity of these important materials. With this data base with which to assess the results of the Viking labeled release simulation studies, it should be possible to gain important insights into the mechanisms of surface reactivity for this important chemical reaction. The results to be gained from these studies will provide a significant body of ground base truth from which to assess: the presence of smectite clays on Mars; the mineralogical form in which the Martian iron is bound; establish upper limits on the present surface water content of Martian soils; perhaps provide insights on the Martian surface radiation history; and to make strong predictions about the nature of surface chemistry on Mars, if iron-bearing clays are a significant component of the surface mineralogical assemblage.

Coyne, Lelia M.↗
NASA NTRS1987

Plagioclase-rich inclusions in carbonaceous chondrite meteorites - Liquid condensates?

The characteristics and formation of coarse-grained, plagioclase-rich inclusions are investigated. The textures, mineralogical compositions, and initial Al-26/Al-27 ratios for the plagioclase-rich inclusions are described. It is observed that plagioclase-rich inclusions in carbonaceous chondrites are either Ca-Al-rich inclusions (CAIs) composed of 30-60 vol pct anorthite, and less than 35 vol pct Ti-Al-pyroxene and melilite, or CA chondrites composed of plagioclase, pyroxene, olivine, spinel, and melilite. It is observed that CA chondrules are chemically and mineralogically the most similar components shared by carbonaceous and ordinary chondrites. The textural changes observed in the inclusions are examined. The data reveal that the CAIs have three textural groups: coarse anorthite laths, equigranular anorthite and Ti-Al-pyroxene, and lacy Ti-Al-pyroxene and fine-grained anorthite.

Wark, D. A.↗
NASA NTRS1987

Possible temperature variation effects on the interpretation of spatially resolved reflectance observations of asteroid surfaces

In virtue of the extent to which the visible and near-IR spectral reflectance of minerals that may be encountered on asteroid surfaces is a function of temperature, surface temperature distributions must be taken into account in the mineralogical evaluation of spectral reflectance data obtained from a spatially resolved asteroid surface. Possible errors of this type are presently illustrated for the case of a silicate mineral assemblage measured at the various temperatures that may be encountered over an asteroid surface, in order to allow optimal mineralogical data extraction.

Roush, Ted L.↗
NASA NTRS1987

Effective use of principal component analysis with high resolution remote sensing data to delineate hydrothermal alteration and carbonate rocks

Methods of applying principal component (PC) analysis to high resolution remote sensing imagery were examined. Using Airborne Imaging Spectrometer (AIS) data, PC analysis was found to be useful for removing the effects of albedo and noise and for isolating the significant information on argillic alteration, zeolite, and carbonate minerals. An effective technique for using PC analysis using an input the first 16 AIS bands, 7 intermediate bands, and the last 16 AIS bands from the 32 flat field corrected bands between 2048 and 2337 nm. Most of the significant mineralogical information resided in the second PC. PC color composites and density sliced images provided a good mineralogical separation when applied to a AIS data set. Although computer intensive, the advantage of PC analysis is that it employs algorithms which already exist on most image processing systems.

Feldman, Sandra C.↗
NASA NTRS1987

Mapping hydrothermally altered rocks in the Northern Grapevine Mountains, Nevada and California with the airborne imaging spectrometer

Seven flightlines of Airborne Imaging Spectrometer (AIS) data were analyzed for an area of hydrothermally altered rocks. The data were reduced to reflectance relative to an average spectrum, and an automated procedure was used to produce a color coded image displaying absorption band information. Individual spectra were extracted from the AIS images to determine the detailed mineralogy. Two alteration types were mapped based upon mineralogy identified using the AIS data. The primary alteration type is quartz sericite pyrite alteration which occurs in northwest-trending zones in quartz monzonite porphyry. The AIS data allow identification of sericite (muscovite) based upon a strong absorption feature near 2.21 micron and weaker absorption features near 2.35 and 2.45 micron. The second alteration type occurs as a zone of argillic alteration associated with a granitic intrusion. Montmorillonite was identified based on a weak to moderate absorption feature near 2.2 micron and the absence of the two absorption features at longer wavelengths characteristic of sericite. Montmorillonite could be identified only where concentrations of sericite did not mask the montmorillonite spectrum.

Kruse, Fred A.↗
NASA NTRS1987

The distribution of evaporitic weathering products on Antarctic meteorites

White evaporite deposits of terrestrial origin occur on some 5 percent of Antarctic meteorites. The few previous studies, and new mineralogical analyses, indicate that the deposits are predominately carbonates and/or sulfates of magnesium. The distribution of white evaporitic salt deposits differs among different meteorite compositional groups and weathering categories. Salts occur with unusual frequency on carbonaceous chondrites, and are especially common in carbonaceous chondrites of weathering categories A and B. Among achondrites, weathering categories A and A/B show the most examples of salt weathering. Unlike carbonaceous chondrites and achrondites, most salt-bearing ordinary (H and L) chondrites are from rustier meteorites of weathering categories B, and to a lesser degree, B/C and C. The LL chondrites are conspicuous by their complete lack or any salt-weathering product. Almost two-thirds of all evaporite-bearing meteorites belong to weathering categories, A, A/B, and B. Where chemical and/or mineralogical data are available, there is a persistent suggestion that evaporite formation is accompanied by elemental redistribution from meteorite interiors. Meteorites of weathering categories B, A/B, and even A may have experienced significant element redistribution and/or contamination as a result of terrestrial exposure.

Velbel, Michael A.↗
NASA NTRS1987

Cometary evolution: Clues from chondritic interplanetary dust particles

Cometary and interplanetary dust particles (IDP) are compared, and the mineralogical evolution of comet nuclei is discussed. Chondritic IDP have properties consistent with properties expected for cometary dust. The complex and varied mineralogy of these particles may indicate mineral alteration processes that occur in comet nuclei. Depending on the thermal budget of a comet, the upper few meters of nucleus material may maintain temperatures within regimes of hydrocryogenic (200 to 237 K) and low-temperature aqueous (274 to 400 K) alteration. Thus, layer silicates, carbonates, and sulfates may be important components of cometary dust and, correspondingly are common constituents of chondritic IDPs. Alteration of comet starting materials may be a common occurrence, and depends on the specific physical and chemical properties of each individual comet.

Reitmeijer, F. J. M.↗
NASA NTRS1987

Detectability of minerals on desert alluvial fans using reflectance spectra

The visible and near-infrared reflectance spectra of soil samples collected from desert alluvial and colluvial surfaces in the Cuprite mining district, Nevada, were analyzed. These surfaces are downslope from hydrothermally altered volcanic rocks that contain spectrally characteristic minerals such as alunite and kaolinite. Coarse fractions of the soils on the alluvial fans are mineralogically variable and express the upslope lithologies; fine fractions are remarkably similar mineralogically and spectrally in all samples because of dilution of local mineral components by regionally derived windblown dust. Theoretical models for spectral mixing and for particle-size effects were used to model the observed spectral variations. Diagnostic mineral absorption bands in the spectra of fan materials were enhanced by computationally removing the spectrum of the homogeneous fine-soil component. Results show that spectral mixing models are useful for analyzing data with high spectral resolution obtained by field and aircraft spectrometers.

Shipman, Hugh↗
NASA NTRS1988

Comparison of techniques for discriminating hydrothermal alteration minerals with Airborne Imaging Spectrometer data

Hydrothermal alteration mineralogy in the Tybo mining district of Nevada has been mapped on the basis of high spectral and spatial resolution Airborne Imaging Spectrometer (AIS) data, using band ratios, principal component analysis, and a signature-matching algorithm to delineate the alteration zones and limestone foundations. The signature-matching algorithm is found to be the most effective method of discriminating alteration minerals, and is noted to be able to identify mineralogy by matching AIS image spectra with library reference spectra. AIS bands in the 2048-2337-nm portion of the spectrum accounted for the greatest amount of variance.

Feldman, Sandra C.↗
NASA NTRS1988

Analysis of chondritic interplanetary dust thin-sections

Chondritic interplanetary dust particles (IDPs) are heterogeneous aggregates of predominantly submicron mineral grains and carbonaceous material, whose bulk compositions agree within a factor of two with type CI/CM carbonaceous chondrites. The mineralogy and petrography of 25 such particles were studied by analytical electron microscopic examination of ultramicrotomed thin sections (500-1000 A thick). Four classes of chondritic IDPs were recognized, referred to as pyroxene, olivine, smectite, and serpentine, and their relative abundances were 9:4:10:2, respectively. Quantitative thin-film analyses indicate that pyroxene particles most closely resemble material emitted from comet Halley. Smectite particles may have formed from pyroxene particles by aqueous alteration of glass and enstatite crystals. Serpentine particles are the only class that are similar to the matrices of carbonaceous chondrites, but these are the least abundant chondritic IDPs. Collectively, chondritic particles are a mineralogically diverse group of extraterrestrial materials.

Bradley, John P.↗
NASA NTRS1988

Atmospheric and surface compositional studies of Mercury and the moon

The atmosphere of the Moon and Mercury will be studied by means of high resolution spectroscopy of sodium and potassium resonance line emissions. The variation of metal vapor abundances with time, and with location will be measured with a view to understanding the origin and evolution of these elements in the atmospheres of the Moon and Mercury. Infrared spectroscopic measurements will be made of Mercury to determine the surface mineralogy, predicated on the availability of the Kuiper Airborne Observatory and infrared charge coupled device (CCD). During the past year, an excellent series of measurements were completed of the spatial distribution of sodium on Mercury. Sodium was found to be concentrated at the polar regions, and to be displaced towards the terminator by solar radiation pressure. Sodium and potassium were discovered in the atmosphere of the Moon. The ratio of sodium to potassium approximates that of the lunar regolith. Thermal infrared measurements of Mercury showed that the Christiansen peak was located shortwards of 8 micrometer, which indicates an acidic mineralogy.

Potter, A. E.↗
NASA NTRS1988

The soils of Mars

A mineralogical model for the Mars fine soil that includes as major components smectite clays absorbed and coated with amorphous iron oxyhydroxides and perhaps mixed with small amounts of better-crystalized iron oxides as separate phases is proposed. Also present as accessory minerals are sulfate minerals such as kieserite (MgSO4.H2O) and/or anhydrite (CaSO4), rutile (TiO2), and maghemite (Fe2O3) or magnetite (Fe3O4), the last two as magnetic components. Carbonates may be present at low concentrations only (less than 1 to 2 pct). However, a prime question to be addressed by a Mars Sample Return Mission shall be related to the mineralogical composition of the soil, and its spatial variability.

Banin, A.↗
NASA NTRS1988

Petrologic constraints on the pressure, temperature, time and composition of the Martian interior

Petrologic analysis of surface samples has been used to deduce pressure and temperature conditions existing in the crust and upper mantle at specific times in the Earth's history, as well as to estimate the chemical and mineralogical composition of the crust and upper mantle. The same techniques can be applied to samples of the Martian surface to provide P, T, time and composition constraints of the Martian interior. Estimates of P and T conditions existing at a given time would, in turn, provide strong constraints on the thermal evolution of Mars. Knowledge of the chemical and mineralogical composition of the Martian interior is of fundamental importance in assessing the early history of the solar system. A general petrological approach is outlined, describing the kinds of sample required, summarizing current understanding of the Martian interior based on experimental petrology, and outlining some of the important experiments needed to allow a full petrologic interpretation of Martian samples.

Holloway, John R.↗
NASA NTRS1988

Geochemistry and origin of gold mineralization in the Kolar Schist Belt

Geological, mineralogical, mineral-textural and geochemical data of the sulfide lodes in the belt indicate that the gold mineralization could be related to low temperature, low Eh and high pH rock-dominated geothermal systems set up in the submarine volcanic pile prior to amphibolite metamorphism. A relatively long-lived geothermal system produced an economic deposit, whereas short-lived ones, because of rapid burial by younger basalts throttled the geothermal system and diffused the discharge yielding low grade ore bodies. The source for gold and iron could be iron enriched tholeiites derived from source regions enriched in komatiitic melt components and komatiitic rocks derived by very low extents of melting of metasomatised mantle sources. On the other hand, the geographical restriction of the quartz-calcite lodes, their mineralogical and geochemical data and their estimated temperature of formation all seem to suggest that a major part of the hydrothermal fluids, and a significant portion of gold could have been derived from mantle derived intrusive, sanukitoid type magma sources, similar to the Champion Gneiss occurring on the eastern part of the belt. However, the possibility of some input by remobilization of a premetamorphic sulfide protore to quartz lodes cannot be ruled out completely.

Siddaiah, N. Siva↗