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NASA NTRS1988

Origin and composition of Mercury

The predictions of the expected range of composition of Mercury at the time of its formation made on the basis of a suite of condensation-accretion models of Mercury spanning a range of condensation temperature and accretion sampling functions appropriate to Mercury are examined. It is concluded that these compositonal models can, if modified to take into account the nonselective loss of most of the silicate component of the planet during accretion, provide compositional predictions for the Weidenschilling (1978, 1980) mechanism for the accretion of a metal-rich Mercury. The silicate portion would, in this case, contain 3.6 to 4.5 percent alumina, roughly 1 percent of alkali oxides, and between 0.5 and 6 percent FeO.

Lewis, John S.↗
NASA NTRS1989

Thermal infrared (2.5-13.5-micron) spectroscopic remote sensing of igneous rock types on particulate planetary surfaces

The compositional significance of outstanding spectral features in the reflectance spectra of particulate igneous rocks was investigated by analyzing directional reflectance spectra, obtained with an FTIR spectrophotometer at 2.17-13.5 microns, of a suite of well-characterized igneous rocks ground to fine particle size. It was found that, using spectral features associated with the principal Christiansen frequency and with a region of relative transparency between the Si-O stretching and bending bands, it is possible to identify general rock type using the Walter and Salisbury (1989) SCFM chemical index, SCFM, defined as SCFM = SiO2/(SiO2 + CaO + FeO + MgO). It is emphasized, however, that the appearance and the wavelength of these features may be affected by environmental factors.

Salisbury, John W.↗
NASA NTRS1989

Spectral characterization of igneous rocks in the 8- to 12-micron region

This paper investigates the crystal-chemistry basis for the variation in spectral behavior of ingneous rocks, with the purpose of developing relationships useful for applications in the lithologic characterization of terrestrial and extraterrestrial surfaces. A new parameter is proposed for characterizing general rock and mineral type. The parameter, SCFM, defined as the ratio SiO2/(SiO2 + CaO + FeO + MgO), reflects the degree of depolymerization of the silica tetrahedra in both fine-grained and coarse-grained igneous rocks, and is a good descriptor of the composition of these rocks. Using spectra obtained in the laboratory on coarse-particulate mineral and solid-rock samples, the SCFM parameter was used to assess the effects of variations in the rock composition on the location, number, and width of spectral bands. A regression analysis of bands varying in width from 0.2 micron to 1.4 microns versus the SCFM value resulted in correlation coefficients ranging from 0.88 to 0.97.

Walter, Louis S.↗
NASA NTRS1989

An olivine-microchondrule-bearing clast in the Krymka meteorite

A small (150 x 200-micron-size) clast consisting of 20 vol pct olivine microchondrules (with barred and granular textures) and 80 vol pct recrystallized silicate matrix material occurs in Krymka (LL3.1). This is the fourth microchondrule-bearing clast to be described. The chondrules are zoned in FeO with concentrations increasing toward the surface. The clast most closely resembles a previously described radial-pyroxene-microchondrule-bearing clast in Piancaldoli (LL3.4).

Rubin, Alan E.↗
NASA NTRS1990

Oxygen isotopes in chondrules and coarse-grained chondrule rims from the Allende meteorite

The relationship between the porphyritic chondrules and coase-grained chondrule rims of the Allende CV chondrite are examined. The oxygen isotopic compositions of seven chondrule-rim pairs and a large rimless refractory chondrule from Allende are determined. The results suggest that, to account for the O-isotopic compositions of the CV chondrules and rims, three solid precursor components are required: a high-temperature, refractory-, alkali, and (O-16)-rich component; a low-temperature, FeO-rich, refractory, and (O-16)-poor component, and an additional component to explain the composition of BO chondrules.

Rubin, Alan E.↗
NASA NTRS1989

Solar nebula chemistry - Implications for volatiles in the solar system

Current theoretical models of solar nebula chemistry which take into account the interplay between chemistry and dynamics are presented for the abundant reactive volatile elements including hydrogen, carbon, nitrogen, oxygen, and sulfur. Results of these models indicate that, in the solar nebula, the dominant carbon and nitrogen gases were CO and NO, whereas, in giant planet subnebulae, the dominant carbon and nitrogen gases were CH4 and NH3; in the solar nebula, the Fe metal grains catalyzed the formation of organic compounds from CO and H2 via the Fischer-Tropsch-type reaction. It was also found that, in solar nebula, bulk FeS formation was kinetically favorable, while FeO incorporation into silicates and bulk Fe3O4 formation were kinetically inhibited. Furthermore, clathrate formation was kinetically inhibited in the solar nebula, while it was kinetically favorable in giant planet subnebulae.

Fegley, Bruce, Jr.↗
NASA NTRS1990

Parental magmas of Mare Fecunditatis - Evidence from pristine glasses

Results are presented on the petrography and electron microprobe analyses of 14 discrete glass beads from the Luna 16 core sample (21036,15) from Mare Fecunditatis regolith, that were previously characterized as representing pristine glasses. Compared to Apollo pristine glasses analyzed by Delano (1986), the Luna 16 pristine glasses have higher CaO and Al2O3 contents but lower MgO and Ni. On the basis of their contents of MgO, FeO, Al2O3, and CaO, these pristine glasses could be divided into two groups, A and B. It is suggested that at least two parental magmas are needed to explain the chemical variations among these glasses. The Group B glasses appear to represent primitive parental magma that evolved by olivine fractionation to the compositions of the Luna 16 aluminous mare basalts, whereas the Group A volcanic glasses may represent an unusual new basalt magma type that contains a high plagioclase component.

Jin, Y.↗
NASA NTRS1991

Enstatite chondrites and achondrites as asteroidal resources

The highly reduced nature of the enstatite meteorites (chondrites and achondrites) differs from that of all other types of stony meteorites. The silicates in the enstatite meteorites contain almost no FeO. In addition, many normally lithophile elements such as Na, Ca, Mg, Cr, and Ti display chalcophilic behavior. A study of the chemistry and mineralogy of the enstatite meteorites was undertaken to determine their resource potential. On average, about 99 percent of the volume of an enstatite achondrite, or aubrite, consists of only four silicate minerals: enstatite, Na-rich plagioclase, diopside, and forsterite, with enstatite being by far the most abundant mineral. The remaining one percent of the volume consists of troilite, kamacite, and trace amounts of oldhamite, daubreelite, ferromagnesian albandite, and schreibersite. Thus, the aubrites can be considered as a possible source for large quantities of Mg, Si, and O, but are of little interest as a source of anything else. The enstatite chondrites appear to be more promising candidates for resource utilization. The chondrites are generally divided into two groups: EH (high iron, fine-grained, with abundant chondrules); and EL (low iron, coarse-grained, with little or no evidence of chondrules). Metallic Ni-Fe makes up roughly 20-25 weight percent of each type of enstatite chondrite. These meteorites are also a good source of nitrogen. This is due in part to the presence of osbornite and sinoite. The latter mineral is restricted to EL chondrites, which typically have a higher bulk nitrogen content than the EH chondrites. Three valuable metals, Cr, Mn, and Ti, are concentrated in a few distinct sulfide phases in the enstatite chondrites. These sulfide phases are troilite and niningerite in EH chondrites and troilite, daubreelite, and ferroan alabandite in EL chondrites.

Hutson, M. L.↗
NASA NTRS1990

Hydrogen, helium, and other solar-wind components in lunar soil - Abundances and predictions

The lack of a shielding atmosphere on the moon permits solar-wind particles to impinge upon the lunar soil and become implanted into the various phases which comprise the soil. Relatively large quantities of solar-wind implanted hydrogen (50-100 ppm) and helium (10-50 ppm) are present. The measured parameter of I(s)FeO, a direct indicator of maturity and exposure age, can be used as a first approximation to predict the abundances of many solar-wind components in the soils. However, because ilmenite acts as a 'sponge' for the retention of certain elements, the TiO2 content of the soil is a better indicator for hydrogen and helium contents.

Taylor, Lawrence A.↗
NASA NTRS1991

Earth's core-mantle boundary - Results of experiments at high pressures and temperatures

Laboratory experiments document that liquid iron reacts chemically with silicates at high pressures (above 2.4 x 10 to the 10th Pa) and temperatures. In particular, (Mg,Fe)SiO3 perovskite, the most abundant mineral of earth's lower mantle, is expected to react with liquid iron to produce metallic alloys (FeO and FeSi) and nonmetallic silicates (SiO2 stishovite and MgSiO3 perovskite) at the pressures of the core-mantle boundary, 14 x 10 to the 10th Pa. The experimental observations, in conjunction with seismological data, suggest that the lowermost 200 to 300 km of earth's mantle, the D-double-prime layer, may be an extremely heterogeneous region as a result of chemical reactions between the silicate mantle and the liquid iron alloy of earth's core. The combined thermal-chemical-electrical boundary layer resulting from such reactions offers a plausible explanation for the complex behavior of seismic waves near the core-mantle boundary and could influence earth's magnetic field observed at the surface.

Knittle, Elise↗
NASA NTRS1991

The Carlisle Lakes-type chondrites - A new grouplet with high Delta(17)O and evidence for nebular oxidation

The petrogenesis of the Carlisle Lakes-type chondrites and their relationship to other chondrites are studied using new petrologic data, especially on mineralogical zoning patterns, and oxygen isotopic analyses of the whole chondrites and some of chondrules. Detailed zoning profiles of mafic silicates are measured in order to determine the environment(s) in which their oxidation states are established. It is concluded that the zoning did not form during crystallization from a melt droplet chondrule but post-dated chondrule formation. Parent-body thermal metamorphism and nebular gas-solid exchange reactions accompanied by condensation of new FeO-rich olivine, utilizing existing olivine surfaces as nucleation sites are considered as hypotheses explaining the zoning. The occurrence of zoned grains in a host that is mainly equilibrated suggests that the equilibration of the Carlisle Lakes-type chondrites occurred prior to final lithification.

Weisberg, Michael K.↗
NASA NTRS1991

Exploration of relationships between low-Ti and high-Ti pristine lunar glasses using an armalcolite assimilation model

The pristine glasses of Delano are the most primitive lunar basaltic magma compositions discovered to date. They are grouped into two (and possibly three) arrays: a low-alumina array and a high alumina array. These glasses are very olivine normative and are multiply saturated at pressures of approximately 20 kbar, implying a depth of origin of 400 to 500 km in the Moon. Thus, these glasses appear to be the best candidates for primitive partial melts of the upper lunar mantle. One of the most perplexing characteristics of the pristine glasses is a positive correlation between Ni and SiO2 within each array. This is contrary to the terrestrial experience, where Ni is observed to positively correlate with MgO and negatively correlate with SiO2. These systematics are believed to be due to the depletion of Ni by olivine fractionation. The difference between the lunar and terrestrial Ni vs. SiO2 trends may be partially ascribed to the Ti-rich component. In the case of the pristine glasses, SiO2 increases not because of olivine fractionation, but because they contain less of the high-Ti component. An attempt was made to model this variation in Ni and SiO2 with a simple assimilation-fractional crystallization (AFC) model. Silica and Ni both decreased dramatically as the AFC process proceeded. Only 15 to 20 percent AFC was necessary to produce the observed variation, and the SiO2 vs. Ni variation was modeled quite well. The D(Ni) for olivine/liquid in this model was taken to be 10 and the olivine was assumed to be Fe sub 80. However, the results of this model for Ti and Mg were less than satisfactory. It seemed difficult to achieve the high TiO2 contents of some glasses (16 to 17 wt. percent) by this method. Continual addition of ilmenite by AFC could indeed raise the titania concentrations to the necessary levels, but only by enriching the magma in FeO and greatly depleting the magma in MgO. An attempt was made to circumvent this problem by using armalcolite, (Fe, Mg)Ti2O5, in the AFC model, and the results are presented.

Jones, John H.↗
NASA NTRS1992

Geochemistry of lunar crustal rocks from breccia 67016 and the composition of the moon

The geochemistry of anorthositic clasts from an Apollo 16 breccia 67016 is studied in order to investigate the role of these rock types in lunar crustal evolution. The samples have aluminous, alkali-poor compositions and varied FeO and MgO contents. Three compositional groups are recognized. One group is poor in mafic constituents with low abundances of lithophile trace elements typical of lunar anorthosites, while the other two groups are more mafic and are distinguished from each other by FeO/MgO ratios greater than one in the case of ferroan noritic and less than one in the case of magnesian troctolitic. These mafic-enriched varieties have considerably higher lithophile element concentrations, at levels similar to that of the bulk lunar crust. The ferroan noritic clasts may represent a fundamental type of igneous rock in the lunar crust which has not been widely recognized.

Norman, Marc D.↗
NASA NTRS1992

Origin of metallic Fe-Ni in Renazzo and related chondrites

To assess the formation of metallic Fe-Ni in Renazzo and related chondrites, Ni and Co zoning profiles in metallic Fe-Ni are determined from different petrographic sites (chondrule interiors, chondrule margins, chondrule rims, and matrix) in Renazzo, Al Rais, and the related chondrite, MacAlpine Hills 87320. Metal from chondrule interiors shows flat Ni and Co concentrations and profiles, moderately large grain-to-grain compositional variations (even with chondrules), and generally high Ni and Co. Nickel concentrations extend above the kamacite stability limit; etching such 'martensite' shows high-Ni domains in some cases, but observed Ni concentrations do not exceed 190 mg/g. Metal from chondrule margins adjacent to matrix shows convex Ni and Co zoning profiles; the highest Ni and Co concentrations are at grain centers, although the mean central Ni and Co concentrations in margin grains are much lower than those from chondrule interiors; the remainder are convex. The low Co and Ni contents at the edge of grains in chondrule margins are interpreted to reflect dilution by Fe produced by FeO reduction.

Lee, Min S.↗
NASA NTRS1992

Olivine in Antarctic micrometeorites - Comparison with other extraterrestrial olivine

The compositions of 5-micron or larger Mg-rich olivines from 26 Antarctic micrometeorite particles were examined and compared with those of other extraterrestrial olivine. The following differences were noted between the Antarctic meteorites and the generally recognized meteorite groups: (1) while refractory-rich (e.g., high Al2O3 or CaO) are common in C2, C3, and UOC meteorites, there are only rare, or possibly no refractory-rich olivines in Antarctic micrometeorites; (2) Mg-rich olivine compositions with FeO less than 1.9 wt pct are underrepresented in the Antarctic micrometeorites, relative to other unequilibrated meteorites; and (3) no Mn-rich, high-Mg olivines were found similar to those described in interplanetary dust, C1, C2, C3, and UOC meteorites.

Steele, Ian M.↗
NASA NTRS1992

Impactites from Popigai Crater

Impactites (tagamites and suevites) from Popigai impact crater, whose diameter is about 100 km, are distributed over an area of 5000 sq km. The continuous sheet of suevite overlies the allogenic polymict breccia and partly authogenic breccia, and may also be observed in lenses or irregular bodies. The thickness of suevites in the central part of the crater is more than 100 m. Suevites may be distinguished by content of vitroclasts, lithoclasts, and crystalloclasts, by their dimensions, and by type of cementation, which reflects the facial settings of ejection of crushed and molten material, its sedimentation and lithification. Tagamites (impact melt rocks) are distributed on the surface predominantly in the western sector of the crater. The most characteristic are thick sheetlike bodies overlying the allogenic breccia and occurring in suevites where minor irregular bodies are widespread. The maximal thickness of separate tagamite sheets is up to 600 m. Tagamites, whose matrix is crystallized to a different degree, include fragments of minerals and gneiss blocks, among them shocked and thermally metamorphosed ones. Tagamite sheets have a complex inner structure; separate horizontal zones distinguish in crystallinity and fragment saturation. Differentiation in the impact melt in situ was not observed. The average chemical compositions of tagamites and suevites are similar, and correspond to the composition of biotite-garnet gneisses of the basement. According to the content of supplied Ir, Ni, and other siderophiles, impact melt was contaminated by 5 percent cosmic matter of collided body, probably ordinary chondrite. The total volume of remaining products of chilled impact melt is about 1750 cu km. Half this amount is represented by tagamite bodies. Though impact melt was in general well homogenized, the trend analysis showed that the concentric zonation is distribution of SiO2, MgO, and Na2O and the bandlike distribution of FeO and Al2O3 content testifies to a certain inheritance and heterogeneity in country rock composition laterally and vertically in the melting zone.

Masaitis, V. L.↗
NASA NTRS1992

The formation of ore mineral deposits on the Moon: A feasibility study

Most of the ore deposits on Earth are the direct result of formation by hydrothermal solutions. Analogous mineral concentrations do not occur on the Moon, however, because of the absence of water. Stratified ore deposits form in layered instrusives on Earth due to fractional crystallization of magma and crystal settling of high-density minerals, particularly chromium in the mineral chromite. We have evaluated the possibility of such mineral deposition on the Moon, based upon considerations of 'particle settling velocities' in lunar vs. terrestrial magmas. A first approximation of Stoke's Law would seem to indicate that the lower lunar gravity (1/6 terrestrial) would result in slower crystal settling on the Moon. However, the viscosity of the silicate melt is the most important factor affecting the settling velocity. The viscosities of typical lunar basaltic melts are 10-100 times less than their terrestrial analogs. These lower viscosities result from two factors: (1) lunar basaltic melts are typically higher in FeO and lower in Al2O3, Na2O, and K2O than terrestrial melts; and (2) lunar igneous melts and phase equilibria tend to be 100-150 C higher than terrestrial, largely because of the general paucity of water and other volatile phases on the Moon. Therefore, particle settling velocities on the Moon are 5-10 times greater than those on Earth. It is highly probable that stratiform ore deposits similar to those on Earth exist on the Moon. The most likely ore minerals involved are chromite, ilmenite, and native FeNi metal. In addition, the greater settling velocities of periodotite in lunar magmas indicate that the buoyancy effects of the melt are less than on Earth. Consequently, the possibility is considerably less than on Earth of deep-seated volcanism transporting upper mantle/lower crustal xenoliths to the surface of the Moon, such as occurs in kimberlites on Earth.

Taylor, Lawrence A.↗
NASA NTRS1992

Moessbauer Spectroscopy for Lunar Resource Assessment: Measurement of Mineralogy and Soil Maturity

First-order assessment of lunar soil as a resource includes measurement of its mineralogy and maturity. Soils in which the mineral ilmenite is present in high concentrations are desirable feedstock for the production of oxygen at a lunar base. The maturity of lunar soils is a measure of their relative residence time in the upper 1 mm of the lunar surface. Increasing maturity implies increasing load of solar wind species (e.g., N, H, and He-3), decreasing mean grain size, and increasing glass content. All these physicochemical properties that vary in a regular way with maturity are important parameters for assessing lunar soil as a resource. For example, He-3 can be extracted and potentially used for nuclear fusion. A commonly used index for lunar soil maturity is I(sub s)/FeO, which is the concentration of fine-grained metal determined by ferromagnetic resonance (I(sub s)) normalized to the total iron content (as FeO). I(sub s)/FeO has been measured for virtually every soil returned by the Apollo and Luna missions to the Moon. Because the technique is sensitive to both oxidation state and mineralogy, iron Moessbauer spectroscopy (FeMS) is a viable technique for in situ lunar resource assessment. Its utility for mineralogy is apparent from examination of published FeMS data for lunar samples. From the data published, it can be inferred that FeMS data can also be used to determine soil maturity. The use of FeMS to determine mineralogy and maturity and progress on development of a FeMS instrument for lunar surface use are discussed.

Morris, R. V.↗