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At least 199 records · Page 11

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NASA NTRS1980

The composition of mesosiderite olivine clasts and implications for the origin of pallasites

The composition of olivine clasts from the mesosiderites Emery, Mincy and Pinnaroo is investigated, and implications of the results for the origin of the pallasites, which, although chemically distinct, may be related to the diogenites, eucrites, howardites and mesosiderites, are discussed. Centimeter-sized olivines were analyzed by electron microprobe, and instrumental neutron activation analysis was performed on one olivine each from Emery and Pinnaroo and an olivine separate from the Brenham pallasite. The olivine compositions are found to range from Fa8 to Fa28, with Emery samples having values from Fa18 to Fa28, and to require essentially total melting of a source composition rich enough in FeO to produce basaltic clasts. It is argued that the mesosiderite olivines were formed in the outer few kilometers of their parent body, as were those of the pallasites, which have the same compositions as the mesosiderite olivines. A model is then developed for the origin of the pallasites as a by-product of igneous differentiation in the external heating of a chondritic parent body.

Mittlefehldt, D. W.↗

NASA NTRS1981

Orthopyroxene-olivine assemblages in diogenites and mesosiderites

Diogenites contain equilibrated orthopyroxene-olivine assemblages. Mn is very regularly partitioned between olivine and orthopyroxene in pallasites, diogenites and synthetic eucrite melts, with an FeO/MnO partition ratio for olivine versus orthopyroxene of 1.6 by weight over a very wide range of FeO contents. In contrast to diogenites, Fe and Mn are not regularly partitioned between the olivine and orthopyroxene of mesosiderites and these minerals were not in equilibrium. Mesosiderite olivine differs from diogenite olivine in Fe/Mn and Ca/Mn ratios. Lack of olivine-orthopyroxene equilibrium suggests that olivine in mesosiderites was derived not from a pyroxenite component analogous to diogenites but from dunites.

Hewins, R. H.↗

NASA NTRS1981

Chondrules in H3 chondrites - Textures, compositions and origins

Compositional and textural variations among chondrules in unequilibrated (type 3) H-group chondrites are examined in order to determine possible relations between chondrule compositions and textures. Bulk compositions of polished thin sections of 90 individual chondrules and 16 compound chondrule sets from the Sharps, Tieschitz and Bremervorde chondrites were measured by broad-beam electron probe analyses; the chondrules were also classified petrographically as barred olivine, porphyritic olivine, porphyritic pyroxene, barred pyroxene, radiating pyroxene or fine-grained. The mean compositions of each type are found to be distinct as verified by discriminant analysis, despite a large scatter, with the olivine-rich chondrules characterized by low SiO2 and high FeO and MgO contents, greater concentrations of TiO2, Al2O3, Na2O and K2O, and lower Cr2O3 and MnO relative to pyroxene-rich chondrules. Data suggest that composition, together with cooling rate, has played a conspicuous role in producing observed chrondrule textures, and are consistent with chondrule formation from mixtures of differing fractions of high-, intermediate- and low-temperature nebular condensates that underwent melting in space.

Lux, G.↗

NASA NTRS1980

Clouding of pyroxene and plagioclase in eucrites - Implications for post-crystallization processing

The clouding of pyroxene and plagioclase in the basaltic eucrites ALHA 77302, Juvinas, Pasamonte, and Stannern, is caused by finely disseminated inclusions. This clouding is interpreted to be the result of exsolution of minor components which became incompatible and crystallized on microfractures and other nucleation sites during postbrecciation metamorphism. The phases found in clouding require reduction of silicate FeO to metallic Fe in both pyroxene and plagioclase and possible redox of Cr(2+) to Cr(3+) in pyroxene. The assemblage of coexisting phases that make up clouding record conditions of T approximately equal to 900 C and f(O2) of 10 to the -16th to 10 to the -18th during slow cooling. Thus, clouding can be a useful indicator of postcrystallization conditions.

Harlow, G. E.↗

NASA NTRS1980

Depositional and irradiational history of the Hadley Rille core 15010/11

Soils from the 15010/11 double drive tube collected at the edge of Hadley Rille have been analyzed for FeO concentrations, I(s)/FeO maturity index values, and noble gas isotopic abundances. Cosmogenic noble gases indicate a total cosmic ray exposure age of less than about 300 million years for the core soils, and it is found that while the production profile of these gases as a function of depth is not consistent with single-stage, in situ irradiation, it is in keeping with pre-irradiated soils deposited or exposed within the past 100 million years. Although significant isotopic differences due to mass fractionation exist on the lunar surface, the solar noble gases in most core soils show little or no evidence of long-term isotopic changes.

Bogard, D. D.↗

NASA NTRS1982

Evidence for aqueous alteration in a carbonaceous xenolith from the Plainview /H5/ chondrite

The compositions of the mineral components of two inclusions within a CM-like clast in the Plainview (H5) chondrite are determined. The inclusions have the morphologies of an Allende-like, coarse-grained CAI and an amoeboid olivine inclusion, respectively. Major constituents of the altered inclusions are found to be calcite, Mg-Fe-rich phyllosilicates, Fe-Ti oxides, and an Al-rich phyllosilicate, and it is suggested that the alteration process would have required transport of Ne, Cl, H2O, CO2, and FeO. Liquid water appears to be the medium in which the alterations took place, due to the presence of hydrous phases and significant quantities of iron required to produce the mineral assemblages now present from the inferred starting materials.

Nozette, S.↗

NASA NTRS1982

The significance of Cl/P2O5 ratios from lunar samples

The Cl(r)/P2O5 ratios of lunar samples are reported to occur in three groups (Jovanovic and Reed, 1975; etc.). These data have been modeled as representative of three discrete volumes of differentiating magma and correlated with large convection cells and moon-wide heterogeneities. The assumptions inherent to their model are not valid. That the Cl(r)/P2O5 ratio of apatite or a rock is indicative of a magma system is unrealistic. A range of ratios can be generated during the fractionation of a magma. Apatite is not the major Cl- and P-bearing phase in most of the samples analyzed; rust, FeO(OH, Cl) and schreibersite, (FeNi)3P, occur in over 2/3 rds of the Apollo 16 rocks where they constitute 0.1-0.6 modal %, enough to account for most of the Cl(r) and P2O5 analyzed. Due to the complexities and presence of these minerals in soils and breccias, Cl(r)/P2O5 ratios have no real significance in non-igneous samples. However, basaltic rocks alone do not define any statistically significant Cl(r)P2O5 groupings.

Taylor, L. A.↗

NASA NTRS1982

A chemical study of individual green glasses and brown glasses from 15426 - Implications for their petrogenesis

Systematic chemical analyses of individual Apollo 15 green glasses were performed in order to: (1) study chemical variations among them; (2) understand their petrogenesis and source region; and (3) study their possible relationships with mare basalts in general. Brown glasses were also analyzed in order to study their chemical variations and their petrogenetic relationships to green glasses and mare basalts. The chemical composition of green and brown glasses is shown and variation diagrams of Sc, Cr2O3, FeO, and Co abundances in green glasses are presented. Igneous fractionation, two component magma mixing, and partial melting of heterogeneous source materials are alternate scenarios to explain strong observed correlations. The composition of green glasses indicates that they were derived by partial melting of the fractionated cumulate source materials formed from a magma ocean which had experienced certain degrees of olivine and plagioclase fractional crystallization.

Ma, M.-S.↗

NASA NTRS1982

Flow behavior of ten iron-containing silicate compositions

The viscosity of ten iron-containing silicates has been measured over the temperature range 400 to 650 C. The compositions contain trace amounts up to 30 wt. pct. or 20 mole. pct. Fe3O4 from 10 to 20 wt. pct. or 10 to 20 mole. pct. Na2O and the remainder is SiO2. Samples were melted in air to form oxidized samples, in forming gas (95% N2-5% H2) to form mildly reduced samples, and in forming gas with carbon in the batch to form strongly reduced samples. In general, the viscosity decreased with increasing mole. pct. Na2O and decreasing mole. pct. SiO2 for a given temperature. In samples with increasing mole. pct. FeO(x) the difference in the viscosity between the oxidized sample and the reduced sample grew in magnitude at a given temperature. In all of the compositions, the log or viscosity, vs reciprocal-of-temperature relation shows curvature with an apparent activation energy between 90 and 100 kcal/mole.

Klein, L. C.↗

NASA NTRS1982

On the location of acid-hydrolysable carbon in lunar soil fines

Soil fines exposed on the lunar surface accumulate small metallic iron particles and solar wind-derived carbon. In previous work, it has been suggested that an intimate association exists between one particular carbon phase, hydrolysable carbon, and very fine iron droplets, where the carbon is in solid solution in the iron. The earlier hypothesis of a constant carbon in iron concentration across a broad range of droplet sizes is testable by combining hydrolysable carbon determinations with a variety of magnetic measurements sensitive to different droplet diameters. New measurements of ferromagnetic resonance response on density and magnetic separates from size fractions of soil 12023 are interpreted as evidence that hydrolysable carbon is preferentially associated with the larger, magnetically stable single-domain iron particles rather than with the smaller superparamagnetic droplets. For the former, there is a quite uniform ratio of iron to carbon both within a series of separates from a single soil, and among soils of widely varying FeO content.

Fallick, A. E.↗

NASA NTRS1982

A new LL3 chondrite, Allan Hills A79003, and observations on matrices in ordinary chondrites

Allan Hills A79003 is an LL3 chondrite with a petrologic subtype of 3.4 + or - 0.2. Contrary to previous suggestions, it is not paired with other Allan Hills specimens. It contains haxonite, (Fe,Ni)23C6; shock-melted, 'fizzed' metal-troilite intergrowths; and translucent, glassy-looking Huss matrix (fine-grained, Fe-rich silicate matrix), in addition to the normal opaque and recrystallized varieties of Huss matrix. Some chondrules are partly coated with opaque matrix, others with translucent matrix. Translucent matrix is more uniform in composition and contains less S, CaO and FeO and more MgO than the opaque variety. Both kinds of matrix rimmed chondrules before consolidation of the meteorite.

Scott, E. R. D.↗

NASA NTRS1982

Trace element concentrations in the isotopically unique Allende inclusion, EK 1-4-1

The bulk sample and mineral separates of the isotopically unique Allende inclusion, EK 1-4-1, are analyzed by instrumental neutron activation for the concentrations of REE, Sc, Fe, Co, Cr, Na, and Ir, and REE concentrations were also determined by mass spectrometric isotope dilution for two density separates. Results show that the inclusion is enriched in light REE compared to heavy REE with a positive Yb anomaly, and has a high Cr concentration, both of which indicate group II affinity, although EK 1-4-1 is a coarse-grained group I inclusion. On the other hand, high Ir, and Sc, and low FeO and Co concentrations were found in the bulk inclusion, and low Na concentrations were found in mineral separates, which indicate an affinity to group I. In addition, for melilite and pyroxene fractions REE, Sc, Co, and Fe were determined to have distributions that were substantially different from those observed for normal Allende type B inclusions.

Nagasawa, H.↗

NASA NTRS1982

Fine, nickel-poor Fe-Ni grains in the olivine of unequilibrated ordinary chondrites

Nickel-poor Fe-Ni grains smaller than 2.0 microns are common inclusions in ordinary, unequilibrated chondrites' porphyritic chondrule olivine, where the olivine grains seem to be relicts that survived chondrule formation without melting. This 'dusty' metal, whose most common occurrence is in the core of olivine grains having clear, Fe-poor rims, appears to be the product of the in situ reduction of FeO from the host olivine, with H2 or carbonaceous matter being the most likely reductants. H2 may have been implanted by solar wind or solar flare irradiation, but this requires the dissipation of nebular gas before the end of the chondrule formation process. Carbonaceous matter may have been implanted by shock. The large relict olivine grains may be nebular condensates or fragments broken from earlier chondrule generations.

Rambaldi, E. R.↗

NASA NTRS1982

Experimental determination of the spinel-garnet boundary in a Martian mantle composition

The high pressure reaction orthopyroxene + clinopyroxene + spinel to garnet + olivine is applicable to the mantle of Mars. Experimental reversals of this reaction in the system CaO-MgO-FeO-Al2O3-SiO2 have been made in the range 1000-1200 C using the bulk composition proposed by Morgan and Anders (1980). At 1000 C, 1100 C, and 1200 C the garnet-out equilibrium is bracketed at 10.8 + or - 0.5, 12.6 + or - 0.5, and 15.2 + or - 0.5 kbars, respectively. A dP/dT slope of 14.0 bar/K at 1000 C increasing to 26.0 bar/K at 1200 C has been inferred. Depending on bulk composition, the mantle of Mars is inferred to have a phase assemblage of either olivine + clinopyroxene + orthopyroxene + garnet or olivine + clinopyroxene + garnet + spinel. In the second, the partial melts will not be buffered by olivine and orthopyroxene and will have markedly lower silica activities than those of the terrestrial mantle.

Patera, E. S.↗

NASA NTRS1982

The Apennine Front core 15007/8 - Irradiational and depositional history

The Apennine Front core 15007/8 was subjected to ferromagnetic resonance (FMR), magnetic and noble gas measurements. Ferromagnetic resonance intensity I(s)/FeO surface exposure (maturity) index values and FeO concentrations are reported for 0.5 cm depth intervals, and noble gas and FMR data are given for 13 soils and two clasts selected from various depths in the 57 cm-long core. These data indicate four core units whose contacts are at about 18, 49 and 55 cm. The 0-18 cm unit has cosmogenic Xe-131/Xe-126 values that are higher than underlying soil and indicate irradiation at depths greater than 50 cm, showing it to probably be the ejecta from the crater on whose rim the core was collected. The 18-49 cm unit has relatively constant I(s)/FeO values and cosmogenic gas abundances, and may represent a mixed soil zone. I(s)/FeO drops by 30 units at the 49-cm contact. Comparison of the 15007/8 core to other ones suggests that soils on slopes tend to be mixed and to not contain units with long in situ radiation profiles.

Bogard, D. D.↗

NASA NTRS1982

Sulfide saturation of basalt and andesite melts at high pressures and temperatures

When the sulfur content of an Fe-bearing magma exceeds the saturation limit for the bulk composition, an immiscible iron sulfide melt fraction separates. For an understanding of the geochemistry of sulfur-bearing magmatic systems, more information is needed regarding the solubility of metal sulfide in silicate melt at its source and the solubility changes as a function of changing intensive and extensive variables. In the present investigation, the sulfur saturation surface is determined for the pressure range from 12.5 to 30 kbar and the temperature range from 1300 to 1460 C for three silicate melt compositions representing a range of SiO2 and FeO compositions.

Wendlandt, R. F.↗

NASA NTRS1983

Stillwater anorthosites - A lunar analog?

Samples of anorthosite from Stillwater complex units AN-I and AN-II have been studied by instrumental neutron activation analysis for FeO, CaO, Na2O, REE, and other trace elements, and the results are discussed. No systematic variations of chemical composition with stratigraphic position were observed. The major and trace compositions of both units appear to be identical, with plagioclase compositions virtually constant throughout both. Thus, there is almost no evidence for evolution of parent magma composition during the genesis of these units. The bulk of the anorthosites appear to consist of cumulus-adcumulus plagioclase and pyroxene. Very little trapped liquid component was found. The chemical elements are not normally or lognormally distributed among samples taken from either anorthosite unit. The irregular distribution of pyroxene oikocrysts indicates that interstitial melt migrated substantially prior to final consolidation of the rock.

Salpas, P. A.↗

NASA NTRS1984

Geochemical evidence for the formation of the Moon by impact induced fission of the proto-Earth

Geochemical evidence is discussed which advocates the theory that the Moon was formed by impact induced fission of the Earth. The Earth's mantle exhibits a number of geochemical peculiarities which make our planet a unique object in the solar system. Terrestrial basalts are compared with those from the Eucrite parent body and the Shergotty parent body. Also the Moon's composition is very close to the Earth's in all details except the lower FeO content which is explained. Evidence is discussed for the plausible physical process of formation of the Moon by impact induced fission. Also the theory that impact induced fission occurred at the moment at which accretion of the Earth was not totally complete is briefly discussed.

Waenke, H.↗