Engineering topics

Shearer, C. K.

Publications and source records attributed to Shearer, C. K..

At least 73 records · Page 4

NASA NTRS1999

Olivine in Martian Meteorite Allan Hills 84001: Evidence for a High-Temperature Origin and Implications for Signs of Life

Olivine from Martian meteorite Allan Hills (ALH) 84001 occurs as clusters within orthopyroxene adjacent to fractures containing disrupted carbonate globules and feldspathic shock glass. The inclusions are irregular in shape and range in size from approx. 40 microns to submicrometer. Some of the inclusions are elongate and boudinage-like. The olivine grains are in sharp contact with the enclosing orthopyroxene and often contain small inclusions of chromite The olivine exhibits a very limited range of composition from Fo(sub 65) to Fo(sub 66) (n = 25). The delta(sup 18)O values of the olivine and orthopyroxene analyzed by ion microprobe range from +4.3 to +5.3% and are indistinguishable from each other within analytical uncertainty. The mineral chemistries, O-isotopic data, and textural relationships indicate that the olivine inclusions were produced at a temperature greater than 800 C. It is unlikely that the olivines formed during the same event that gave rise to the carbonates in ALH 84001, which have more elevated and variable delta(sup 18)O values, and were probably formed from fluids that were not in isotopic equilibrium with the orthopyroxene or olivine The reactions most likely instrumental in the formation of olivine could be either the dehydration of hydrous silicates that formed during carbonate precipitation or the reduction of orthopyroxene and spinel If the olivine was formed by either reaction during a postcarbonate beating event, the implications are profound with regards to the interpretations of McKay et al. Due to the low diffusion rates in carbonates, this rapid, high-temperature event would have resulted in the preservation of the fine-scale carbonate zoning' while partially devolatilizing select carbonate compositions on a submicrometer scale. This may have resulted in the formation of the minute magnetite grains that McKay et al attributed to biogenic activity.

Shearer, C. K.↗

NASA NTRS1996

Diogenites: Cumulates from Asteroid 4 Vesta: Insights from Orthopyroxene and Spinel Chemistry

Cumulate rocks are important planetary lithologies, but they can be difficult to interpret. Important clues to the nature of their parental melts may still be present in the interiors of cumulus phases. However, in some cases, even the cores of the cumulus grains may have been modified by postcrystallization reactions with trapped melt and other cumulus phases. We have previously studied the major-, minor-, and trace-element chemistry of orthopyroxene from a suite of diogenites and concluded that their chemical attributes can best be explained by crystallization from parental melts that were derived from a depleted mantle source that had already experienced eucrite removal. However, we and others have had difficulty explaining the great range in concentration of minor elements (Al, Ti) and trace elements (REE, Y, Zr) if all diogenites were derived from a single magmatic system. Therefore, we have investigated the chemistry of diogenitic spinels to see if they still held clues to the diogenite parental melt compositions. Although spinel is low in abundance in diogenites (<5 vol%) it still may hold clues to the maomatic and metamorphic history of these rocks.

Papike, James J.↗

NASA NTRS1994

Orthopyroxene as a recorder of lunar crust evolution: An ion microprobe investigations of Mg-suite norites

The lunar Mg suite, which includes dunites, troctolites, and norites, could make up 20-30% of the Moon's crust down to a depth of 60 km. The remainder is largely anorthositic. This report focuses on norites because we have found that the chemical characteristics of orthopyroxene are effective recorders of their parental melt compositions. Many of the samples representing the Mg suite are small and unrepresentative. In addition, they are cumulates and thus are difficult to study by whole-rock techniques. Therefore, we decided to study these rocks by SIMS techniques to analyze a suite of trace elements in orthopyroxene. The 12 norite samples were selected from a recent compilation by Warren who attempted to select the best candidate samples from the standpoint of their pristine character. Our present database includes greater than 300 superior Electromagnetic Pulse (EMP) analyses and greater than 50 scanning ion mass spectroscopy (SIMS) analyses for 8 Rare Earth Elements (REE), Zr, Y, and Sr. The Mg#s for the parental melts calculated from Mg#s in orthopyroxene show that most melts have Mg#s in the range of 0.36-0.60. This compares with a range of Mg#s for lunar volcanic picritic glass beads of 0.4-0.68. Therefore, although the cumulate whole-rock compositions of the Mg suite can be extremely magnesian, the calculated parental melts are not anomalously high in Mg. A chemical characteristic of the Mg-suite norites that is more difficult to explain is the high KREEP content of the calculated parental melts. The REE contents for the calculated norite parental melts have REE that match or exceed the high-K KREEP component of Warren. Therefore, mixing of a KREEP component and a picritic melt cannot, by itself, explain the high estimated REE contents of the melts parental to norites. Advanced crystallization following KREEP incorporation, especially of plagiclase, may also be required.

Papike, J. J.↗

NASA NTRS1994

Orthopyroxene as a recorder of primitive achondrite petrogenesis: Major-, minor-, and trace-element systematics of orthopyroxene in Lodran

Considerable attention has been paid recently to the primitive achondrites because they may form a link between chondrites and more differentiated achondrite meteorites. A recent paper by Miyamoto and Takeda addresses the thermal history of lodranites Yamato 74357 and MAC 88177 as inferred from chemical zoning of pyroxene and olivine determined by electron microprobe analyses. Their results suggested that interstitial melt was present and then extracted. We have taken the analysis of Lodran-type meteorites one step further by incorporating the techniques of Electromagnetic Pulse/Wavelength Dispersive Spectroscopy (EMP/WDS) compositional imaging and scanning ion mass spectroscopy (SIMS) analysis. Orthopyroxene in Lodran is strongly zoned in CaO, Al2O3, TiO2, and Cr2O3 within the last 10-30 microns from the grain boundaries. The rims are reversely zoned in Mg-Fe, exhibiting Mg enrichment, and compositions change from a fairly uniform Wo3En94 within the grains to Wo1En96 at the rims. CaO drops from 1.6 to 0.6 wt% and Al2O3, TiO2, and Cr2O3 exhibit similar depletions. MnO is fairly uniform throughout the grains at around 0.5 wt%. Olivine is also reversely zoned with respect to not only grain boundaries but also to fractures within the grains, giving many olivine grains a complex, patchy zoning pattern. Some of the core-rim trace-element systematics for orthopyroxene are illustrated. Because of the rather narrow zoned rims in Lodran orthopyroxene and the low trace-element abundances, it is difficult to clearly resolve the trace-element systematics. Nevertheless it is evident that the cores are enriched in the incompatible trace elements Ce, Nd, Dy, Er, Yb, Y, and Zr relative to the rims.

Papike, J. J.↗

NASA NTRS1993

Orthopyroxenes as recorders of diogenite petrogenesis: Major and minor element systematics

As a part of our research to better understand magmatic processes in the Eucrite Parent Body, we have initiated an ambitious program of study of major, minor and trace elements in orthopyroxene from diogenites. This paper reports preliminary results for major and minor elements in orthopyroxenes for a suite of 13 diogenites: Aioun El Atrouss, ALH 84001, ALH A 77256, EET 87530, Ellemeet, Garland, Ibbenburen, Johnstown, Manegoan, peckelsheim, Roda, Shalka, and Tatahouine. A companion paper by Shearer et al. reports new trace element data for ALH 84001, ALH A 77256, Ibbenburen, and Tatahouine. We have presently collected over 800 high quality pyroxene microprobe analyses for Si, Al, Ca, Na, Mn, Fe, Mg, Cr, and Ti. The chemical systematics observed for these orthopyroxenes reflect original magmatic mineral/melt partitioning plus later trapped liquid/mineral equilibration, subsolids, exsolution, and mineral/mineral metamorphic reactions. We have therefore avoided, at this point, any attempt to use statistical analysis to group (e.g. factor or cluster analysis) these orthopyroxenes chemically.

Papike, J. J.↗

NASA NTRS1993

Basaltic magmatism on the Moon. A perspective from volcanic picritic glasses

It is widely accepted that basaltic magmas are products of partial fusion of peridotite within planetary mantles. As such they provide valuable insights into the structure and processes of planetary interiors. Those compositions which approach primary melt compositions provide both a clearer vision of planetary interiors and a starting point at which to understand basaltic evolution. Within the collection of lunar samples returned by the Apollo and Luna missions are homogeneous, picritic glass beads of volcanic origin. These glass beads provide a unique perspective concerning the origin of mare basalts, the characteristics of the lunar interior, and processes culminating in the early differentiation of the moon. In this presentation, we report our ion microprobe derived trace element data from all picritic glasses previously identified. We place this trace element data and literature isotopic and experimental data on the picritic glasses with the framework of mare basaltic magmatism.

Shearer, C. K.↗

NASA NTRS1993

Origin of the Apollo 15 very low Ti green glass. A perspective from the compositional diversity in the very low Ti glasses

The very low Ti green glasses from the Apollo 15 site have intrigued scientists for over 20 years. Their primitive composition has been used to understand magmatic processes and the structure of the moon. The compositional variability observed in the Apollo 15 glass population has long been a point of debate. Initial studies did not recognize the compositional diversity in the glasses. Stolper et al. documented the major element variability and concluded it could not be produced by magmatic processes and therefore concluded that these glasses must be of impact origin. Subsequent studies confirmed a volcanic origin for the glass population and attempted to elucidate magmatic processes to account for its compositional variability. Models that have been proposed for these glasses include the following: (1) the crystallization of single or multiple phases (olivine, pyroxene, Fe metal, immiscible sulfide); (2) the incompatible behavior of Ni and Co during multiple phase crystallization at extremely low fO2; and (3) magma or source mixing. All of these models have problems. Type (1) models appear not to be consistent with recent trace element studies on the glasses; model (2) is dependent on the debatable incompatible behavior of Ni and Co, and, in models of type (3), the origin and nature of mixing models are somewhat unconstrained. This study compares the Apollo 15 green glasses with the very low Ti picritic glasses from other landing sites.

Shearer, C. K.↗

NASA NTRS1993

Orthopyroxenes as recorders of diogenite petrogenesis: Trace element systematics

Eucrite, howardite, and diogenite members of the achondrites are considered, by many, to be genetically related. Therefore, each provide a piece of the puzzle for reconstructing magmatic processes on the eucrite parent body (EPB). The relationship between eucrites and diogenites can be viewed within the context of two distinctly different models: (1) fractional crystallization; and (2) partial melting. In fractional crystallization models, eucrites and diogenites represent a complementary continuum of planetary fractional crystallization products in which the diogenites represent crystal accumulations during the crystallization of eucritic magmas at shallow to deep levels in the EPB. Alternatively, experimental studies may be interpreted as indicating eucrites represent peritectic partial melts of a primitive, chondritic EPB mantle. Within this type of model, the diogenites are also generally considered to be cumulates; however, their petrogenetic relationship to the eucrites is less clear. Sack et al. proposed that the olivine diogenites represent residua from the partial melting events that produced eucritic liquids. Initial trace element studies of orthopyroxene (OPX) are consistent with this model. However, this trace element modeling of the olivine diogenites is nonunique. As a further test of these models, we did the following three things: (1) analyzed OPX from cumulate diogenites to compare with the olibine diogenite data; (2) improved ion microprobe analytical techniques for the analysis of elements critical to our interpretations; and (3) selected more relevant Kd's for OPX-eucritic melt.

Shearer, C. K.↗

NASA NTRS1991

Exploring the lunar mantle with secondary ion mass spectrometry - A comparison of lunar picritic glass beads from the Apollo 14 and Apollo 17 sites

Results are presented from SIMS analyses of major, minor, and trace elements in lunar picritic glass beads obtained from the Apollo 14 (A-14) and Apollo 17 (A-17) landing sites. The results obtained indicate that the glasses from each site differed significantly in their Ba/Sr and light-REE/heavy-REE ratios. The differences between the A-14 and the A-17 glasses appear to be the result of a higher KREEP component in all the A-14 glasses, indicating that the mantle source of the A-14 site is intrinsically different from the A-17 mantle source.

Shearer, C. K.↗

NASA NTRS1990

Inter- and intra-group compositional variations in Apollo 15 pyroclastic green glass - An electron- and ion-microprobe study

Results are presented on major- and trace-element abundance analyses of Apollo 15 pyroclastic green glasses from groups A, B, C, D, and E, carried out using electron- and ion-microprobe techniques. The diagrams depicting Sr, Zr, Ba, and Nd vs Co variations indicate the presence of a high-Co trend in groups A and D and a low-Co trend in groups B and C. Group-E glasses were found to be significantly enriched in Sr, relative to the other four glass groups. Chemical data of this study were integrated with previous data to evaluate various magmatic processes that have been proposed in the past to explain chemical variations in the lunar green glass. Results of calculations using a source mixing model suggest that the Apollo 15 green glasses represent multiple eruptive events from three chemically distinct but compositionally variable source regions.

Galbreath, K. C.↗

NASA NTRS1990

A SIMS study of lunar 'komatiitic glasses' - Trace element characteristics and possible origin

In Apollo 16 regolith breccias, Wentworth and McKay (1988) identified a suite of minute (less than 120 microns) 'komatiitic glass beads'. The wide major element compositional range, and ultra-Mg-prime character of the glasses suggest a variety of possible origins from complex impact processes to complex volcanic processes involving rather unusual and primitive magmatism. The extent of trace element depletion or enrichment in these glasses appears to be correlated to the siderophile character of the element (ionization potential or experimentally determined silicate melt/Fe metal partition coefficients. The ultra-Mg-prime glasses are depleted in Co relative to a bulk Moon Mg/Co exhibited by many lunar samples (volcanic glasses, basalts, regolith breccia, estimated upper mantle). The low Co and high incompatible element concentrations diminish the possibility that these glasses are a product of lunar komatiitic volcanism or impact, excavation, and melting of a very high Mg-prime plutonic unit.

Shearer, C. K.↗

NASA NTRS1990

Ion microprobe studies of trace elements in Apollo 14 volcanic glass beads - Comparisons to Apollo 14 mare basalts and petrogenesis of picritic magmas

Results are presented from trace element analysis, by ion microprobe techniques, of individual glass beads representing seven compositionally distinct types of picritic glass beads from the Apollo 14 landing site. The picritic glass beads at the A-14 exhibited a wide range of primary magma compositions and a lack of petrogenetic linkage (via crystal fractionation) to crystalline basalts. The wide range of major and trace element characteristics of the picritic glass beads is consistent with derivation from mineralogically distinct sources which consist of varying proportions of olivine + orthopyroxene +/- clonopyroxene +/- ilmenite +/- plagioclase +/- KREEP component.

Shearer, C. K.↗

NASA NTRS1989

Is plagioclase removal responsible for the negative Eu anomaly in the source regions of mare basalts?

The nearly ubiquitous presence of a negative Eu anomaly in the mare basalts has been suggested to indicate prior separation and flotation of plagioclase from the basalt source region during its crystallization from a lunar magma ocean (LMO). Are there any mare basalts derived from a mantle source which did not experience prior plagioclase separation? Crystal chemical rationale for REE substitution in pyroxene suggests that the combination of REE size and charge, M2 site characteristics of pyroxene, fO2, magma chemistry, and temperature may account for the negative Eu anomaly in the source region of some types of primitive, low TiO2 mare basalts. This origin for the negative Eu anomaly does not preclude the possibility of the LMO as many mare basalts still require prior plagioclase crystallization and separation and/or hybridization involving a KREEP component.

Shearer, C. K.↗

NASA NTRS1989

An ion microprobe study of the intra-crystalline behavior of REE and selected trace elements in pyroxene from mare basalts with different cooling and crystallization histories

The effects of crystallization interaction on the trace element zoning characteristics of pyroxenes are analyzed using electron and ion microprobe techniques. Four pigeonite basalts with similar isochemical composition, but different cooling rates and crystallization histories are studied. Pyroxene quadrilaterals displaying crystallization trends are presented. The crystal chemical rationalization of REE zoning, pattern shapes, and abundances are examined. The data reveal that the trace element zoning characteristics in pyroxene and the partitioning of trace elements between pyroxene and the melt are related to the interaction between the efficiency of the crystallization process, the kinetics at the crystal-melt interface, the kinetics of plagioclase nucleation and the characteristics of the crystal chemical substitutions in the pyroxene and the associated crystallizing phase.

Shearer, C. K.↗

NASA NTRS1989

Petrology of Apollo 14 regolith breccias and ion microprobe studies of glass beads

Mineral chemistries, glass chemistries, and bulk compositions of Apollo 14 regolith beccias are used to study the regolith evolution at the Apollo 14 site and on the moon in general. Major changes in the regolith since the formation of the breccias include an increase in maturity, an increase in glasses with the Fra Mauro basalt composition, and decreases in feldspathic and mare glasses. The results suggest the presence of a source with a larger non-KREEPy highland plutonic component than other breccias.

Simon, S. B.↗

NASA NTRS1984

Petrology of Apollo 11 regolith breccias

Petrographic and mineral chemical data for 16 Apollo 11 regolith breccias show that: (1) the regolith breccias differ from soil 10084 with respect to agglutinate content, glass population, plagioclase compositions, and proportions of high-K mare and low-K mare basalt components; (2) the A-11 breccias and soil have highland components that are similar both in abundance and petrology; and (3) lunar regolith breccias provide a better comparison with howardites than do lunar soils. The data and observations are consistent with formation of the regolith breccias from immature soil. It appears that little or no highland material has been added to the Tranquillitatis regolith since the formation of the breccias.

Simon, S. B.↗

NASA NTRS1983

Petrology of the Apollo 11 highland component

New data for 38 highland fragments hand-picked from Apollo 11 coarse fines are reported. Petrographic, mineralogic, and bulk chemical data show that: (1) the Apollo 11 highland component is non-KREEPy and like that of Apollo 16; (2) poikilitic rocks, granulitic breccias, and the anorthosite-norite-troctolite suite are the most abundant rock types, followed by polymict breccias and glasses; (3) both the ferroan anorthosite and Mg-rich plutonic suites are represented in the Apollo 11 highland component; (4) except for one sample, the intermediate-K Fra Mauro and high-K Fra Mauro groups are not represented. The data and observations are consistent with local derivation of the highland material from beneath relatively thin basalt flows and addition to the regolith via vertical mixing.

Simon, S. B.↗

NASA NTRS1983

Chemistry of the Apollo 11 highland component

Thirty-eight Apollo 11 lunar highland fragments from coarse fines 10085 have been subjected to petrologic and chemical study. Six major chemical groups are identified: (a) high-K KREEP; (b) anorthosite with a 10X chondrite positive Eu anomaly and anorthosite with 30X positive Eu anomaly; (c) ANT; (d) LKFM; (e) anorthositic gabbro with no Eu anomaly, with a positive Eu anomaly, and with a negative Eu anomaly; and (f) dominant Highland component, 2X-10X chondrite with a positive 10X-14X Eu anomaly. Newly recognized groups are presented based on the REE patterns: (a) ANT group with 5X La and a 22X positive Eu anomaly; (b) 10X flat with 14X positive Eu anomaly; and (c) 2-3X flat with a 10X positive Eu anomaly. The highland suite is very low in K and REE, and is overall quite similar to the Apollo 16 suite.

Laul, J. C.↗