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At least 127 records · Page 7

Formational history of lunar rocks - Applications of experimental geochemistry of the opaque minerals

Experimental data on the cooling histories of lunar rocks are presented along with a descriptive mineralogy of certain opaque minerals in Apollo 17 samples. Lunar rocks having Zr partitionings of coexisting ilmenite and ulvospinel indicative of high-temperature equilibrium (above 1000 C) appear to have cooled rapidly to temperatures below 800-900 C. The Ti content of troilite coexisting with ilmenite can be used to differentiate rock fragments which are mineralogically and texturally similar. It is found that Cr and Mg partitionings between coexisting armalcolite and ilmenite vary notably between rocks so that they can be used to distinguish otherwise similar samples. The spinels are analyzed as varieties of chromian ulvospinel and titanian chromite.

Taylor, L. A.

Light element geochemistry of the Apollo 17 site

Abundances of C, N, S, He, H, and metallic iron at Taurus-Littrow are typical of a mixed mare and highland environment. Isotopic compositions of C, N, and S also generally conform to patterns observed elsewhere on the moon. Further evidence is presented for a complex lunar S cycle.

Petrowski, C.

Geochemistry and the origin of life

The origin of life on earth is examined from a viewpoint stressing the validity of the concept of chemical evolution. The different geological formations supporting the mechanisms of the theory are described; the stage of chemical evolution (preceding that of biological evolution) would have taken place from the time of the origin of the earth and meteorites, 4.6 billion years ago, to the early Precambrian period, about 3.2 billion years ago. Specific aspects of the problem discussed include amino acids from spark discharges and their comparison with the Murchison meteorite amino acids, the properties and theory of genesis of the carbonaceous complex within the cold Bokevelt meteorite, ammonion ion concentration in the primitive ocean, the oxygen isotope chemistry of ancient charts, the origin and rise of oxygen concentration in the earth's atmosphere, Precambrian microorganisms and evolutionary events prior to the origin of vascular plants, and biogenicity and significance of the oldest known stromatolites.

Kvenvolden, K. A.

Geochemistry of biomolecules

A highly sensitive fluorometric technique is developed for the determination of biological and geo-organic compounds in ancient sediments and extraterrestrial samples. This technique is used to establish chemical evidence for fossil pigments in an extraterrestrial sample. Also developed is a highly sensitive and specific fluorometric method for the determination of total primary amine nitrogen in soil samples.

Bonner, J.

Geochemistry

The most effective strategy for the geochemical study of a planet is to proceed systematically with the mineralogical and chemical characterization of its materials in accordance with geologically determined priorities. It is insufficient merely to analyze chemically the surface rocks. To appreciate the meaning of a chemical analysis, some assessment must be made of the geologic history of the sample - what its source and mode of origin are and what processes have operated upon the sample to cause chemical fractionation. Determination of mineralogy, texture, lithology, and other properties of the rock that might be relevant to origin is, therefore, necessary.

Carr, M. H.

Light element geochemistry of the Apollo 15 site

Abundances of C, N, S, and He and contents of CH4 and metallic Fe at Hadley-Apennine are typical of a mixed mare and highland environment. Isotopic compositions of C, N, and S similarly conform in most cases to patterns observed elsewhere on the moon. Systematic relationships between S abundance and total Fe content are apparent for crystalline rocks from most landing sites but their full significance is not yet understood.

Kaplan, I. R.

Geochemistry of grain-size fractions of soils from the Taurus-Littrow valley floor

Results are presented for a study in which high-precision instrumental neutron activation analysis was applied to determine the abundances of seven rare-earth and nine other elements in two grain-size fractions (90 to 150 microns and less than 20 microns) of eight soils from the Taurus-Littrow Valley floor and one Apollo 11 bulk-soil fraction with grain sizes of less than 1 mm. Compositional differences between the two size fractions of two valley-floor soils are examined, and mixing of soil components is investigated. It is found that a five-component mixing model describes very adequately the chemical composition of bulk soils with grain sizes of less than 1 mm as mixtures of local Apollo 17 rock types (basalt, anorthositic gabbro, noritic breccia), orange glass, and meteorites, but does not describe well the chemical compositions of the other two size fractions. A ten-component model is used to show that the compositions of those two size fractions can be well represented as mixtures of the five components if the mineralogy and chemical composition of the basalt component are allowed to vary in the size fractions.

Korotev, R. L.

Rare earth and trace element geochemistry of a fragment of Jurassic seafloor, Point Sal, California

Rocks from an ophiolite suite once on the seafloor were analyzed for rare earth elements (REE), Sc, Co, Na2O, Cr, Zn and FeO. Strontium isotope exchange noted in some of the lavas is attributed to basalt-seawater interaction; the Ce abundance in smectite- and zeolite-bearing lavas may also be due to prolonged exposure to seawater. The higher grades of metamorphic rock, however, show no variation from the usual flat or slightly light REE depleted profiles. Plutonic igneous rock, all light REE depleted, have total REE abundances varying by a factor of 100 between the dunites and diorites. In order of decreasing REE abundance are hornblende, clinopyroxene, plagioclase, orthopyroxene and olivine. Calculations of REE contents of liquids in equilibrium with early cumulative clinopyroxenes suggest that the parent to the stratiform sequence was more depleted in light REE than the parent to the lava pile.

Menzies, M.

Light element geochemistry of the Apollo 12 site

Analytical techniques of improved sensitivity have revealed details of the concentrations and isotopic compositions of light elements for a comprehensive suite of samples from the Apollo 12 regolith. These samples show a wide spread in maturity, although maximum contents observed for solar wind elements are less than observed at other sites, possibly reflecting relative recency of craters at the Apollo 12 site. Isotopic composition of nitrogen is consistent with the idea that N-15/N-14 in the solar wind has increased with time, at least a major part of this increase having occurred in the past 3.1 Gyr. Sulfur isotope systematics support a model in which sulfur is both added to the regolith, by meteoritic influx, and lost, by an isotopically selective process. Most soils from this site are heavily contaminated with terrestrial carbon.

Kerridge, J. F.

Trace element geochemistry and the early lunar differentiation

The results are considered of experiments in which thermal neutron activation analysis was used to measure the halogens, U, Te, Ru, Os, and Hg in lunar samples. A calorimetric method was used for P2O5. Three Apollo 17 basalts, one Apollo 11 basalt, and one Apollo 15 basalt were used for the Ru-Os study. Os and Ru were measured in seven samples of breccia 14305 in a series of experiments to check an apparent anomaly in the isotopic composition of the Hg which it contains. A lunar model for Ru-Os partition is discussed. It is suggested that Ru and Os were partitioned and fractionated in the original differentiation of the lunar surface ocean. Fractionation among near-surface materials was less than a factor of 2 according to the lithic breccia data. Fractionations among basaltic sources were very large, exceeding 100, and primarily due to Ru. A clue to Ru and Os distributions at the depths from which mare basalts were derived may be provided by the relative ages of the basalts. These are interpreted as being related to partial melting in response to temperature increases at depth with time.

Jovanovic, S.

The petrology and geochemistry of impact melts, granulites, and hornfelses from consortium breccia 61175

The matrix and 58 clasts from breccia 61175 were analyzed for major, minor, and trace elements. The matrix is anorthositic and has lithophile trace element abundances 20 to 40 times chondrite. Clasts comprise impact melt rocks, xenocryst and xenolith-free very high aluminum (VHA) and anorthositic basalts, anorthosite, anorthosite-norite-troctolite granulites, and hornfelses. The VHA and anorthositic basalts are considered to be impact melts, and the hornfelses were probably formed by incorporation of breccias or preexisting melt rocks into a melt sheet prior to cooling. The range of melt-rock lithophile trace element abundances might indicate more than one melt sheet.

Winzer, S. R.

Petrology and geochemistry of lithic fragments separated from the Apollo 15 deep-drill core

Petrological and geochemical analysis of lithic fragments separated from the Apollo 15 deep-drill core showed these fragments to fall into the essentially the same range of rock types as observed in surface soil samples and large rock samples. Three particles are singled out as being of special interest. One sample is a mare basalt containing extremely evolved phases. The particle may represent small-scale imperfect crystal/liquid separation in a lava flow. A green glass particle is not the ultramafic emerald green glass described from the Apollo 15 site, but rather an ANT-like light green color, and has a quite different chemical composition from the ultramafic variety. One mare basalt displays a positive Eu anomaly and is enriched in plagioclase relative to olivine plus pyroxene.

Lindstrom, M. M.

Carbonaceous chondrites. II - Carbonaceous chondrite phyllosilicates and light element geochemistry as indicators of parent body processes and surface conditions

Petrographic analyses of CM matrices characterized four phyllosilicates in Murray and Murchison meteorites and Fe- and Mg-serpentines in Nogoya. All phyllosilicates and bulk matrices show enrichment of K relative to Na when compared with bulk meteorites; the loss of Na and some Cl, and the addition of H2O, CO2, and water-soluble organics during alteration indicates a partially open system. Synthesis of soluble organic materials may have occurred in CM matrices before aqueous alteration of the precursive phases. Nogoya was 95% altered and has a bulk C content of 5.2%, higher than any meteorite; also, it has the lowest measured C-13/C-12 ratio of any carbonaceous chondrite except for Karoonda.

Bunch, T. E.