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At least 145 records · Page 8
All sourcesNASA NTRSDOE OSTI
NASA NTRS1972

Applications of activation analysis to geochemical, meteoritic and lunar studies.

The application of activation analysis techniques to the analysis of cosmological materials, i.e., terrestrial, tektitic, meteoritic, and lunar matter, is reviewed. Elemental determinations can be made by instrumental fast-neutron and thermal-neutron activation analysis, photonuclear and charged-particle activation analysis, and by radiochemical neutron activation analysis. Partition-coefficient methods, autoradiography studies, gamma-gamma coincidence counting, and age determination by neutron activation are discussed. Attention is given to K-Ar and I-Xe dating of meteorites.

Showalter, D. L.↗
NASA NTRS1973

Apollo 15 and 16 results of the integrated geochemical experiment.

A number of experiments carried in orbit on the Apollo 15 and 16 spacecraft were used in the compositional mapping of the lunar surface. The observations involved measurements of secondary (fluorescent) X-rays, gamma rays and alpha particle emissions. A large scale compositional map of over 20% of the lunar surface was obtained for the first time. It was possible to demonstrate significant chemical differences between the mare and the highlands, to find specific areas of high radioactivity and to learn something about the composition of the moon's hidden side.

Adler, I.↗
NASA NTRS1973

Ultraminiature X-ray fluorescence spectrometer for in-situ geochemical analysis on Mars.

A spectrometer based upon the X-ray fluorescence method of elemental analysis has been developed in an ultraminiature, rugged form suitable for a spacecraft mission to Mars. The instrument employs two radioisotope sources (Fe-55 and Cd-109) which irradiate adjacent areas on a regolith sample. Fluorescent X rays emitted by the sample are detected by four thin-window proportional counters. Using pulse-height discrimination, the energy spectra are determined. Virtually all elements above sodium in the periodic table are detected if present at sufficient levels. Minimum detection limits range from 30 ppm to 2% depending upon the element and the matrix. For most elements, they are below 0.5%. Accuracies also depend upon the matrix, but are generally better than plus or minus 0.5% for all elements of atomic number greater than 14. Elements below sodium are also detected, but as a single group. Ambiguities of identification of the elements producing the observed spectra are minimal.

Clark, B. C.↗
NASA NTRS1974

On the petrological, geochemical, and geophysical characterization of a returned Mars surface sample and the impact of biological sterilization on the analyses

A study was conducted: to identify those experiments that could and should be done on a returned Martian sample in order to characterize its inorganic properties; to evaluate, insofar as can be done, the effects of potential biological sterilization of the sample by heating prior to its return; to identify particular analytical techniques needing further improvement in order to make optimum use of a returned sample; and to identify experiments to be done on simulants, with and without sterilization, that better define the limits of information available about the planet from analyses of returned samples.

Source record↗
NASA NTRS1974

Geochemical affinities of cobalt and germanium toward metal, silicate, and sulfide phases at high temperature

Hydrothermal studies indicate that Co and Ge are strongly siderophile when metallic iron is in equilibrium with olivine at 900 C and 500 bars. If the metal is replaced by troilite (FeS), Ge is strongly lithophile whereas Co tends to concentrate in the sulfide phase. If iron meteorites were formed in a core derived from the sulfide phase, they would be depleted in Ge but retain Co.

Wai, C. M.↗
NASA NTRS1976

Martian volatiles - Their degassing history and geochemical fate

Implications of the Ar-40 content of the Martian atmosphere for Martian volatile history are considered. It is assumed that the potassium content of both Mars and earth is similar to that of normal chondrites, that Mars possesses a water content similar to that of normal chondrites, and that earth's water content is equal to or somewhat less than Mars'. A simple earth-analogous Mars degassing model is outlined in which the Martian surface volatile inventory is presumed to be identical to earth's, but scaled to the smaller mass and surface area of Mars. Physical storage of volatiles in the Martian regolith is examined along with the occurrence of volatile-containing mineral phases in the regolith, exospheric escape as a massive volatile sink, and the effect of the time history of degassing on the surface volatile inventory. Implications of earth's degassing history for Mars are assessed, and models describing the overall intensity of Mars degassing are presented. It is concluded that the maximum amounts of water and other volatiles that could be stored in the Martian regolith are marginally compatible with those required by the earth-analogous model, although a lower atmospheric Ar-40 concentration and regolith volatile inventory would be easier to reconcile with observational constraints.

Fanale, F. P.↗
NASA NTRS1976

Mineralogic and petrologic implications of Viking geochemical results from Mars - Interim report

Chemical results from four samples of Martian fines delivered to Viking landers 1 and 2 are remarkably similar in that they all have high iron; moderate magnesium, calcium, and sulfur; low aluminum; and apparently very low alkalies and trace elements. This composition is best interpreted as representing the weathering products of mafic igneous rocks. A mineralogic model, derived from computer mixing studies and laboratory analog preparations, suggests that Mars fines could be an intimate mixture of about 80% iron-rich clay, about 10% magnesium sulfate (kieserite), about 5% carbonate (calcite), and about 5% iron oxides (hematite, magnetite, maghemite, goethite). The mafic nature of the present fines (distributed globally) and their probable source rocks seems to preclude large-scale planetary differentiation of a terrestrial nature.

Baird, A. K.↗
NASA NTRS1977

Diterpenoid compounds and other lipids in deep-sea sediments and their geochemical significance

Cyclic diterpenoid compounds have been found by various investigators in the geosphere (e.g., fossil resins, coals, soil, shale, and deep-sea sediments). These compounds occur in significant amounts only in higher plants and are therefore potential markers of terrigenous plant lipids. Diterpenoids with the abietane skeleton (mainly dehydroabietic acid) have been identified in the lipids of sediment samples from the northeast Pacific Ocean, Black Sea, and North Atlantic Ocean. The presence of these resin-derived compounds was correlated with the terrigenous clay components and with the presence of pollen. The presence of polycyclic diterpenoids was also correlated with the distribution patterns and inferred sources of other sediment lipid constituents. Potamic transport, followed by turbidite redistribution, is the probable input mechanism of these resin-derived compounds to the deep-sea sediments. These diterpenoids appear to be excellent biological markers of resinous higher plants.

Simoneit, B. R. T.↗
NASA NTRS1977

Geochemical zoning and early differentiation in the moon

The volatile elements (e.g., Rb, Pb, Tl, Bi, Cs) seem to have been depleted at the time of lunar accretion. Accordingly, it may be assumed that the moon initially accreted from refractory material. The good correlation between volatile/involatile element ratios (e.g., Cs/U, K/La, K/Zr) in both highland and maria samples means that element distribution in lunar crustal rocks is not governed by volatility differences. This and other evidence encourages the view that the moon was accreted homogeneously. A consequence of homogeneous accretion theories is that very efficient large-scale element fractionation is required to account both for the high near-surface concentrations of refractory elements (e.g., Th, U, REE, Zr, Ba, etc.) and for the Ca-Al-rich crust.

Taylor, S. R.↗
NASA NTRS1977

Time scale for the formation of the earth and planets and its role in their geochemical evolution

The initial mass of the solar nebula is discussed. Models of a massive nebula (two solar masses and more) encounter serious difficulties: an effective mechanism of transfer of the momentum from the central part of the nebula outward, capable of leading to formation of the sun and removal of half the mass of the nebula from the solar system has not been found. As a consequence of the instability of these models, their evolution can end with the formation, not a planetary system, but of a binary star. The possibility is demonstrated of obtaining acceptable growth rates for Uranus and Neptune by prolonging the thickening of preplanetary dust in the region of large masses. The important role of large bodies in the process of formation of the planets is noted. The impacts of such bodies, moving in heliocentric orbits, could have imparted considerable additional energy to the forming Moon, which, together with the energy given off by the joining of a small number of large protomoons, could have led to a high initial temperature of the moon.

Safronov, V. S.↗
NASA NTRS1977

Geochemical studies of the White Breccia Boulders at North Ray Crater, Descartes region of the lunar highlands

The samples of the White Breccia Boulders obtained during the Apollo 16 mission and investigated in the reported study include an anorthositic breccia (67415), a dark matrix breccia (67435), a light matrix breccia (67455), and a large clast of dark matrix breccia (67475) taken from the 67455 boulder. The chemical analyses of bulk samples of the samples are listed in a table. A graph shows the lithophile trace element abundances. Another graph indicates the variation of Sm with Al2O3 content for samples from the White Breccia Boulders. The North Ray Crater breccias are found to be in general slightly more aluminous than breccias from the other stations at the Apollo 16 site. Analyses of eight Apollo 16 breccias cited in the literature range from 25% to 35% Al2O3. However, the North Ray Crater breccias are more clearly distinct from the other Apollo 16 breccias in their contents of lithophile trace elements.

Lindstrom, M. M.↗
NASA NTRS1975

A geochemical and petrographic study of 1-2-mm fines from Apollo 17

Samples of fines less than 1-mm and 155 1-2 mm particles from several Apollo 17 sites were analyzed for Na, Sc, Cr, Mn, Fe, Co, Ni, Hf, Ta, Th, and REE. Products of comminution and construction are present in the 1-2 mm particles, and the compositions of the rock fragments clearly indicate the general chemical characteristics of their parent rock types. The likely sources of materials for the glassy particles are considered. Glasses are enriched over their parent soils in Fe, Sc, Mn, and Cr, and are relatively enriched in light REE, so that some chemical fractionation accompanies glass-forming processes. Elements were determined by instrumental neutron activation analysis.

Blanchard, D. P.↗
NASA NTRS1975

Geochemical and geological units of Mare Humorum - Definition using remote sensing and lunar sample information

Mare Humorum has been found to contain at least nine distinct units. Mare basalt units typical of those at the Apollo 12 and 15 sites and central Mare Serenitatis exist also in Mare Humorum, but the early, high-titanium basalts typical of Mare Tranquillitatis and southeast Mare Serenitatis are absent. Basalts containing about 5% TiO2, not sampled at any Apollo site, also are found in Mare Humorum. Emplacement of extensive low-titanium basalts occurred in Mare Humorum in roughly the same period as emplacement of similar basalts at Apollo 12 and central Mare Serenitatis. These were followed by emplacement of the higher titanium basalts during a later period. These and other units are characterized and their extent mapped using a combination of remote sensing and Apollo sample studies. The results are interpreted in the context of the evolution of the Humorum region.

Pieters, C.↗
NASA NTRS1975

Photogeological, geophysical, and geochemical data on the east side of the moon

Correlations between Apollo orbital data and geologic data for eight map provinces are reported for a region centered on the east limb of the moon (50 deg N to 50 deg S and 50 deg E to 140 deg E). The appearance of the provinces is described, and the basins in or near the region are assigned relative ages. The western (nearside) part of the region averages about 3 km lower in elevation than the eastern (farside) part, according to laser altimeter measurements which are used to make geologic cross sections. Gravity data correlate with most geologic provinces and the surface profiles made by the laser altimeter and lunar sounder. The distribution of concentration ratios of Al/Si and Mg/Si as well as the distribution of relatively low natural radioactivity are considered.

El-Baz, F.↗
NASA NTRS1978

Organic geochemical studies on kerogen precursors in recently deposited algal mats and oozes

The same kerogen-like residue from the algal mats and oozes at Laguna Mormona, Baja California, is examined following degradation by saponification, alkaline KMnO4 oxidation, and HBr treatment. For comparison, pyrolytic degradation is performed for the residue and five others, two of which are obtained from algal mats at Baffin Bay, Texas. Major conclusions are that (1) Saponification of a residue specimen from the algal-ooze residue results in minor amounts of components bonded to it as esters; (2) Alkaline KMnO4 oxidation reveals that the same residue consists of a cross-linked aliphatic nucleus with additional components attached to it as esters; (3) the major products from pyrolysis of the residue include phytenes, pristenes, sterenes, and triterpenes; and (4) the HBr treatment yielded only one product, indicating the absence of a large number of ether-linkages readily cleaved by HBr.

Philp, R. P.↗