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At least 487 records · Page 27
All sourcesNASA NTRSDOE OSTI
NASA NTRS1983

Chondrules and other components in C, O, and E chondrites Similarities in their properties and origins

Three types of chondrules are described that are common to H3, LL3, CM2, CO3, and CV3 chondrites. Low- and high-FeO, porphyritic olivine chondrules contain olivine with Fa0.3-8 and Fa5-50 respectively, and can easily be distinguished petrographically. Poikilitic pyroxene chondrules have 1-20 vol pct olivine (Fa0.2-8) enclosed by low-Ca pyroxene (Fs0.5-7), and also occur in E chondrites. These three types formed in separate nebular regions which had dimensions and spacings such that a few percent of the chondrules that collided to form compound chondrules were of different types. Sorting of chondrule precursor material and mixing of chondrule types probably account for most variations in bulk and mineral chemistry among chondrite groups. Metallic Fe,Ni grains containing 0.1-1 percent Cr, Si, and P are present in low-FeO olivine chondrules from all type 2 and least metamorphosed type 3 chondrites. Metal compositions reflect reduction during chondrule formation in the nebula, not nebular condensation. Opaque matrices in type 3 ordinary and carbonaceous chondrites are somewhat similar in composition and mineralogy, and probably have related origins. It is concluded that chondrules in all known chondrite groups share similar nebular origins.

Scott, E. R. D.↗
NASA NTRS1984

Strain analysis of the Leoville chondrite and conditions in asteroidal interiors

Deformed chondrules in the Leoville carbonaceous chondrite define a preferred orientation, also recognized previously in other CV3 chondrites. Identifying the strain mechanism is necessary for understanding the conditions which caused this compressional shortening. Luckly, the major mineralogical constituent of CV3 meteorites is olivine, for which experimental data on strain mechanisms exist. The conditions that caused strain in the olivine were obviously applicable to the whole meteorite. Possible mechanisms of olivine deformation are cataclasis, low temperature plasticity, power low creep, and diffusional flow, each of which occurs under different combinations of temperature and deviatoric stress. Cataclasis can be ruled out on the basis of its high deviatoric stress requirements; some fractures occur in chondrule olivines, but these may have formed during excavation or impact. Low temperature plasticity and power low creep occur by means of various types of lattice dislocations. However, methods of thermal decoration and chemical etching of dislocations failed to indicate evidence for either mechanism. Thus, the inference is that diffusional flow, characteristic of low to moderately high temperatures and low deviatoric stress, was the major deformation mechanism.

Cain, P. M.↗
NASA NTRS1985

Cathodoluminescence zoning and minor elements in forsterites from the Murchison (C2) and Allende (C3V) carbonaceous chondrites

Cathodoluminescence has been applied to look for textural features of olivine in carbonaceous meteorites relevant to the unresolved dispute over the origin of the olivine, whether from a vapor or a liquid. Cathodoluminescence photographs of forsterite grains in Murchison (C2) and Allende (C3) meteorites presented here reveal a blue core with planar boundaries to a red or dark rim. High-precision electron microprobe analyses have been performed which reveal unusually large amounts of the 'minor' elements Al, Ti, and Ca in the blue cores of these forsterites, suggesting formation by crystallization at high temperatures from a source rich in these metals. Following conclusions drawn from previous analyses of olivine in meteorites, it is argued that the minor element signature should be able to characterize olivines in micrometeorites and in deep-sea particles.

Steele, I. M.↗
NASA NTRS1989

Basalts and gabbros from Mare Crisium - Evidence for extreme fractional crystallization

Petrographic and electron microprobe techniques were used to examine igneous fragments in Luna 24 samples 24088 and 24105. It is the complex chemistry of the pyroxenes that distinguishes the different rock types. Basaltic pyroxenes exhibit an Fe-enrichment trend; the evolutionary trends are more complex in the gabbros, with enrichments in both Fe and Ti and a depletion in Cr. These chemical evolutionary trends are displayed by a progressive variation in rock types from Mg-rich olivine-gabbro to olivine-gabbro, and to ferrogabbro and ferrotroctolite. The low TiO2 content of the primary melt, possibly represented by the least-evolved Mg-rich olivine-gabbro, retarded the formation of early ilmenite and spinel, such that 'Fenner Trend' Fe enrichment occurred. The ferrotroctolite is probably the end product of chemical evolution by extreme fractional crystallization, controlled primarily by olivine and pyroxene crystallization.

Lu, F.↗
NASA NTRS1990

Matrix mineralogy of the Lance CO3 carbonaceous chondrite - A transmission electron microscope study

Results are presented on electron microprobe analyses of three CO chondrites, all of which are falls: Lance, Kainsaz, and Warrenton. The TEM mineralogy results of Lance chondrite show that Fe-rich matrix olivines have been altered to Fe-bearing serpentine and Fe(3+) oxide; matrix metal was also altered to produce Fe(3+) oxides, leaving the residual metal enriched in Ni. Olivine grains in Lance's matrix contain channels along their 100-line and 001-line directions; the formation and convergence of such channels resulted in a grain-size reduction of the olivine. A study of Kainsaz and Warrenton showed that these meteorites do not contain phyllosilicates in their matrices, although both contain Fe(3+) oxide between olivine grains. It is suggested that, prior to its alteration, Lance probably resembled Kainsaz, an unaltered CO3 chondrite.

Keller, Lindsay P.↗
NASA NTRS1990

Complex petrogenesis of the Nakhla (SNC) meteorite - Evidence from petrography and mineral chemistry

The Nakhla (SNC) meteorite, of putative Martian origin, consists of euhedra and subhedra of augite and olivine in a fine-grained basaltic mesostasis. This paper presents petrographic and mineral chemical data on the Nakhla meteorite, which were collected to help distinquish among the four existing hypotheses for the formation of olivine in this meteorite. It is concluded that none of these hypotheses can explain the origins of olivine and augite. A new hypothesis is proposed, which is consistent with the data presented. It suggests that the cores of augites and olivines are both xenocrysts from a partially equilibrated source rock.

Treiman, A. H.↗
NASA NTRS1989

Infrared spectra of crystalline and glassy silicates and application to interstellar dust

The infrared spectra of crystalline minerals predicted in theoretical condensation sequences do not match the astronomical observations. Since the astronomical spectra are a closer match to glassy silicates, the authors undertook a study to measure the infrared spectra of glassy silicates that have compositions similar to silicate minerals predicted in theoretical condensation sequences. The data should support observations aimed at elucidating condensation chemistry in dust forming regions. The authors measured the mass absorption coefficients, from 2.5 to 25 microns, of ground samples of olivine, diopside, and serpentine and also smoke samples that were prepared from these minerals. The smoke samples prepared in this way are predominantly glassy with nearly the same composition as the parent minerals. The crystalline samples consisted of pure olivine ((Fe(0.1)Mg(0.9))(2)SiO(4)), serpentine, diopside. Sample purity was confirmed by x ray diffraction. Each mineral was ground for 10 hours and a measured mass of the powder was mixed with KBr powder for absorption measurements using the method of Borghesi et a. (1985). The smoke samples were prepared from the same samples used for grinding by vaporizing the minerals using pulsed laser radiation in air. The smoke samples formed by condensation of the resulting vapor. The smoke settled onto infrared transparent KRS-5 substrates and onto a quartz crystal microbalance used to obtain mass measurements. A description of the preparation method is given in Stephens (1980). The glassy diopside showed only diffuse electron diffraction peaks and hence was nearly amorphous, while the serpentine smoke showed a weak diffraction pattern corresponding to MgO. The smoke from olivine showed a weak diffraction pattern corresponding to Fe2O3 and/or Fe3O4. The mass absorption coefficients, from 2.5 to 25 microns, of crystalline diopside, olivine, and serpentine and their corresponding smoke samples are shown in figures.

Stephens, John R.↗
NASA NTRS1991

Reflectance spectra of Fe(2+)-Mg(2+) disordered pyroxenes: Implications to remote-sensed spectra of planetary surfaces

The reflectance spectra of Fe(2+)-Mg(2+) disordered orthopyroxenes are relevant to surfaces of terrestrial planets onto which basaltic magma has been extruded. If cooling rates of basalt lava flows were fast, equilibrium iron intersite partitioning may not have been achieved so that abnormal enrichments of Fe(2+) ions in M1 sites would occur. The two intense pyroxene Fe(2+) site CF bands in the 1 micron and 2 micron regions would continue to dominate the the reflectance spectra so that the pyroxene composition and structure type would be readily identified in telescopic spectral profiles. However, abnormal intensification of the Fe(2+)/M1 site CF band at 1.20 microns could lead to the false identification of olivine in remote sensed spectra because in pyroxene-olivine mixtures the inflection around 1.20 microns is the only spectral feature for detecting the presence of olivine. The identification of iron-bearing plagioclase feldspars, too, would be obscured by the pyroxene Fe(2+)/M1 site CF band at 1.20 microns. Such interference would be a major problem if in situ reflectance spectra could be measured on the surface of Venus where ambient temperatures are as high as 475 C. Disordering of Fe(2+) and Mg(2+) ions comparable to that in the orthopyroxenes used in this spectral chemical study might be expected in low Ca pyroxenes occurring on the Venusian surface. Researchers conclude that Fe(2+)/M1 site spectral features need to be carefully assessed in remote-sensed spectra before deductions are made about the presence of olivine on planetary surfaces.

Burns, Roger G.↗
NASA NTRS1991

Reflectance spectra of some fractions of Migei and Murchison SM chondrites in the range of 0.3-2.6 microns

The reddening observed in CM chondrites is not understood. Johnson and Fanale observed that, as CM chondrites are more finely powdered, their spectra become more reddened. In the process of meteorite crushing, the chondrules are broken up. Those authors suggested that in this case the silicate components of the chondrules (mainly olivine), which have higher IR reflectivities, were able to contribute more to the overall spectrum. Gaffey and McCord proposed two possible physical mechanisms which could produce such an effect. But it is also possible that the presence of the organic polymers in the matrix material results in the reddening of the CM spectra. To test these two hypotheses, the matrix material and the material enriched in olivines were separated from Migei and Murchison CM chondrites using a binocular microscope. The spectra of these fractions were compared with the spectra of the bulk samples of Migei and Murchison. The spectra of the most 'clean' Migei matrix fractions indicate that the reddish slopes of CM spectral curves in the near infrared are due to the enhanced olivine feature, rather than to organic matter. The authors propose that the red slope of the spectra of some C-type asteroids may indirectly suggest the presence of olivine in the surface material. At the same time, the red sloped spectra of more distant D-type asteroids seem to be due to the presence of organic materials. If so, then the chemical or physical form of this organic matter must be quite different from the organic materials which would be on the surfaces of the parent bodies of CM chondrites (most likely C-type asteroids). It is also possible that the content of organic components in the CM matrix is too low to change the slope of the spectra.

Moroz, L. V.↗
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

Petrology of basaltic sills from ocean drilling program sites 794 and 797 in the Yamato Basin of the Japan Sea

The basaltic sills from ocean drilling program sites 794 and 797 in the Yamato Basin of the Japan Sea are characterized petrographically on the basis of a detailed study of the composition of relict phenocryst and groundmass phases. The systematic variation in the rock compositions is discussed. Results of 1-atm melting experiments on a relatively primitive basalt from site 797 are reported. The sills are found to constitute two distinct groups of suites: primitive, olivine-bearing suites with low potassium and primitive olivine-bearing to evolved, olivine-free suites with relatively high potassium. A pseudoinvariant reaction relationship between olivine and augite and magnetite is inferred. Complex magmatic and tectonic evolutions in the region, perhaps reflecting a transitional stage between subduction zone activity and back arc spreading, are suggested.

Thy, P.↗
NASA NTRS1993

Micro-zoning in minerals of a Landes silicate inclusion

There is an increasing number of meteorites with chondritic bulk composition but completely different textures than the conventional chondrite groups. Winonaites, Acapulcoites and silicate inclusions in IAB-iron meteorites have in common coarse grain size, highly equilibrated mineralogy with frequent 120 deg triple junctions and they record a significantly lower degree of oxidation than ordinary chondrites. They all have equilibration temperatures, based on Ca-exchange among pyroxenes, of around 900 to 1100 deg C. However, on cooling disequilibrium features may develop: (1) Olivine in IAB-inclusions has lower Fa-content than equilibrium Fs-content of pyroxenes requires; (2) CaO-zoning in olivine was established at temperatures of around 500 deg C, several hundred degrees below pyroxene equilibration temperatures. Obviously, olivine responded faster to changes in fO2 (Fa in olivine) and temperature (Ca-zoning) than pyroxenes. Differences in diffusion coefficients can readily explain the observed trends. Here we report on much more subtle zoning features in pyroxenes. TEM-observations reveal large compositional gradients in Ca, Na, Cr, Ti and Fe within the first micrometer of cpx and opx crystals. In summary, the data reflect the complicated subsolidus history of a chondritic mineral assemblage that was in thermodynamic equilibrium at about 900 deg C and cooled slowly from this temperature whereby oxidation reactions and different closure temperatures for various minerals and elements played an important role. The oxidation of P dissolved in metal and formation of phosphate, which is thermodynamically stable at low temperatures, is suggested to be responsible for most of the observed zoning.

Eisenhour, D. D.↗
NASA NTRS1993

Stalking the LREE-enriched component in ureilites

Ureilites contain a LREE-enriched component whose origin and identity are unknown, but which may have been introduced into 4.55 Ga olivine + pyroxene assemblages at various times in the period 4.55 - 3.74 Ga. This component is volumetrically minor, inhomogeneously distributed, and can be removed with concentrated HNO3, which suggests that it may be contained in minor, interstitial phases not previously recognized in ureilites. There is evidence, however, that not all of this component is leachable. Whole rock samples of Kenna, Novo Urei, and ALHA77257 form a Nd-143/Nd-144-Sm-147/Nd-144 line with a slope corresponding to an age of 3.74 Ga. Although this line could be a mixing line, with one end-member being the LREE-enriched component and the other being a 4.55 Ga olivine + pyroxene assemblage, the observation that a pyroxene separate from Kenna plots on the line suggests that the LREE-enriched component at least partially equilibrated with the olivine and pyroxene and that the line is an isochron. We performed a leaching experiment on Kenna, using various acids and concentrations, in an attempt to isolate the LREE-enriched component and differentiate between possible hosts for it, and to determine whether all of it is leachable. Our results suggest that most of the LREE-enriched component is surface-sited, rather than contained in a discrete mineral. However, some of it is not readily leachable because it equilibrated with Kenna olivine + pyroxene at 3.79 plus or minus 0.05 Ga.

Goodrich, Cyrena Anne↗
NASA NTRS1993

Petrologic models of 15388, a unique Apollo 15 mare basalt

Mare basalt 15388, a feldspathic microgabbro from the Apennine Front, is chemically and petrographically distinct from Apollo 15 picritic, olivine-normative (ON), and quartz-normative basalts. The evolved chemistry, coarse texture, lack of olivine, and occurrence of cristobalite in 15388 argue for derivation by a late-stage magmatic process that is significantly removed from parental magma. It either crystallized from a magma evolved from the more mafic Apollo 15 basalts, or it crystallized from a currently unrepresented magma. Rb-Sr and Sm-Nd isotopic systematics yield isochron ages of 3.391 plus or minus 0.036 and 3.42 plus or minus 0.07 Ga, respectively, and epsilon(sub Nd) = 8.6 plus or minus 2.4, which is relatively high for Apollo 15 mare basalts. In contrast to chemical patterns of average Apollo 15 ON basalts and Apollo 15 picritic basalt, 15388 has a strongly positive LREE slope, high Ti, shallower HREE slope and a slightly positive Eu anomaly. These features argue against 15388 evolution by simple olivine fractionation of a parental ON or picritic basalt magma, although olivine is a dominant liquidus phase in both potential parents.

Hughes, S. S.↗
NASA NTRS1993

The dregs of crystallization in Zagami

The Zagami shergottite is a basaltic meteorite which formed when a phenocryst-bearing lava flow was emplaced at or near the surface of Mars. Recently, a cm-sized olivine-rich lithology has been identified in Zagami by Mossbauer spectroscopy. Olivine is extremely rare in shergottites, particularly in Zagami and Shergotty, where it occurs only as minute grains. We report petrologic and microprobe studies of this olivine-rich lithology. This material represents the last few percent of melt and is highly enriched in phosphates, opaques and mesostases, all of which are late-stage crystallization products. Phosphates replaced augite as a phenocryst phase when the magma became saturated in P. This late stage melt also includes a fayalite-bearing, multi-phase intergrowth which crystallized after the melt became too rich in iron to crystallize pigeonite. We can now reconstruct the entire crystallization history of the Zagami shergottite from a deep-seated magma chamber to crystallization of the final few percent of melt in a near-surface dike or thick flow. Small pockets (tens of microns) of late-stage melt pockets are ubiquitous but volumetrically minor in Zagami. We do not know the physical relationship between these areas and the cm-sized olivine-rich material described here. It is possible that these small pockets were mobile, forming larger areas. Perhaps inspection of the entire hand specimen of Zagami would clarify this relationship.

Mccoy, T. J.↗
NASA NTRS1993

Petrogenesis of Apollo 12 mare basalts. Part 2: An open system model to explain the pigeonite basalt compositions

Original petrogenetic models suggested that the pigeonite basalts were the evolved equivalents of the olivine basalts. Rhodes et al. concluded that the olivine and pigeonite basalts were co-magmatic, but Neal et al. have demonstrated that these two basaltic groups are distinct and unrelated. The pigeonite suite is comprised of porphyritic basalts with a fine-grained ground mass and range continuously to coarse-grained microgabbros with ophitic to graphic textures. Although it was generally recognized that the pigeonite basalts were derived from the olivine basalts by olivine + minor Cr-spinel fractionation, the compositional gap between these groups is difficult to reconcile with such a model. Indeed, Baldridge et al. concluded that these two basaltic groups could not have been co-magmatic. In this paper, we suggest an open system AFC model for pigeonite basalt petrogenesis. The assimilant is lunar anorthositic crust and the r value used is 0.6. While the choice of assimilant composition is difficult to constrain, the modeling demonstrates the feasibility of this model.

Neal, Clive R.↗
NASA NTRS1993

Opaque-rich lithology in the Divnoe achondrite: Petrology and origin

An opaque-rich lithology (ORL) makes up to approximately 9 vol. percent of the Divnoe achondrite. It is characterized by enrichment of troilite and pyroxene, compared to the bulk Divnoe, and by the presence of tiny remnants of olivine in low-CA pyroxene and low minor element concentrations in pyroxene. The ORL was formed by local reaction between gaseous sulfur and olivine in the Divnoe. The Divnoe meteorite is an olivine-rich achondrite with subchondritic chemistry and mineralogy. It has a granoblastic coarse-grained olivine groundmass (CGL: coarse-grained lithology) with relatively large (2-10 mm) poikilitic patches (PP) of pyroxene and, rarely, plagioclase. The groundmass also contains an opaque-rich fine-grained lithology (ORL) which comprises approximately 9 vol. percent of the meteorite, displays reaction boundaries with the groundmass, and differs in mineral chemistry from it. Numerous micron- to mm-thick veins of troilite and, rarely, metal cross all the lithologies found in the meteorite. The Divnoe itself appears to represent a sample of an igneous source region.

Petaev, M. I.↗
NASA NTRS1994

Cooling rates of chondrules: A new approach

Mineralogy and texture of chondrules have been reproduced experimentally and it was demonstrated that the abundance of heterogeneous nuclei is an important factor controlling chondrule textures. Cooling rates of chondrules were estimated from the zoning patterns of olivine. Low cooling rates (less than 100 C/h) yielded chemically homogeneous olivine crystals, whereas higher cooling rates, between 100 and 2000 C/h, produced olivine compositions similar to those observed in natural chondrules. We present a new approach to determining cooling rates of chondrules based on the microstructure of chondrule clinopyroxene and plagioclase. All observations were made on Allende chondrules. Two independent processes (Ca and Mg diffusion in pyroxene and Al/Si ordering in plagioclase) yield similar cooling rates on the order of 10-1 C/h for granular olivine pyroxene (GOP) chondrules in Allende. Our cooling rates are at least one order of magnitude lower than those derived from dynamic crystallization experiments.

Weinbruch, S.↗