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Brannon, J. C.

Publications and source records attributed to Brannon, J. C..

Elevated initial Sr-87/Sr-86 in ordinary chondrite metal

The metal phase of ordinary chondrites has been found to contain a complex assemblage of non-metal phases, evidently formed when elements such as Si, Cr and P, originally dissolved in the metal, were subsequently oxidized and exsolved. We have investigated the Rb-Sr isotopic system in samples of H-chondrite metal, finding small but nontrivial amounts of Sr, apparently concentrated toward the surface of metal grains, and characterized by pronounced excesses of Sr-87/Sr-86 in chondritic metal can plausibly account for the characteristically elevated initial Sr-87/Sr-86 found in ordinary chondrite phosphates, but it remains unclear when and where the metal experienced the high Rb/Sr environment needed to account for such high Sr-87/Sr-86. We have previously reported Rb-Sr data for separated metal from Dhajala (H3), Forest Vale (H4) and Estacado (H6). Here we report data for two size fractions (80-160 and 280-450 microns) of separated metal from the H4 chondrite Ste. Marguerite. These samples were etched twice (.5N HCl for one hour) before dissolution (6N HCl). Aliquots of the solutions were spiked for Fe, Ca and Rb + Sr. The results for Ste. Marguerite metal are presented; errors are two-sigma and elemental concentrations are stated in terms of total sample weight.

Podosek, F. A.↗

Initial Sr-87/Sr-86 and Sm-Nd chronology of chondritic meteorites

Isotopic analyses of the Rb-Sr and Sm-Nd systems in phosphates from ordinary chondritic meteorites (Bjurbole, Mocs, Menow, Elenovka, Ambapur Nagla, and St. Severin) are presented. The Sm-Nd data yield an isochron of age 4.55 + or - 0.45 Ga and an initial Nd-143/Nd-144 consistent with that of Juvinas. Initial Sr-87/Sr-86 ratios are characteristically (possibly excepting St. Severin) elevated with respect to BABI or ALL. Considering both presently and previously reported data, elevation of initial Sr-87/Sr-86 ratios corresponding to metamorphism intervals of the order of 10 to the 8th years seems quite characteristic of chondrites of metamorphic grade 4 or higher. These formation intervals, however, do not correlate with either degree of metamorphism or with I-Xe ages, hence such data for metamorphic chronologies should be interpreted with caution.

Brannon, J. C.↗

Rare earth elements in the sedimentary cycle - A pilot study of the first leg

The effects of source rock composition and climate on the natural abundances of rare elements (REE) in the first leg of the sedimentary cycle are evaluated using a study with Holocene fluvia sands. The medium grained sand fraction of samples collected from first order streams exclusively draining granitic plutons in Montana (semi-arid), Georgia (humid), and South Carolina (humid) are analyzed. It is found that the REE distribution patterns (but not the total absolute abundances) of the daughter sands are very similar, despite compositional differences between parent plutons. Averages of the three areas are determined to have a La/Lu ratio of about 103, showing a depletion of heavy REE with respect to an average granite (La/Lu = 79) or the composition of North American Shales (La/Lu = 55). However, the Eu/Sm ratio in sands from these areas is about 0.22, which is very close to this ratio in North American Shales (0.21), although the overall REE distribution of these sands is not similar to that of the North American Shales in any way. It is concluded that the major rock type, but neither its minor subdivisions nor the climate, controls the REE distribution patterns in first cycle daughter sands, although the total and the parent rock-normalized abundances of REE in sands from humid areas are much lower than those in sands from arid areas.

Basu, A.↗

Major and trace element chemistry of Luna 24 samples from Mare Crisium

Atomic absorption spectrometry and instrumental neutron activation analysis were employed to analyze six Luna 24 soils for major and trace elements. The analysis revealed well-mixed soils, though size fractions of each of the soils showed quite dissimilar compositions. Thus the regolith apparently has not been extensively reworked. Noritic breccia admixed preferentially to the finest size fractions and differential comminution of one or more other soil components accounted for the observed elemental distributions as a function of grain size. The ferrobasalt composition and one or more components with higher MgO contents have been identified in the samples.

Blanchard, D. P.↗

Trace element distribution in mineral separates of the Allende inclusions and their genetic implications

Concentrations of the rare earth elements (REE), Sc, Co, Fe, Zn, Ir, Na, and Cr were determined for mineral separates of the coarseand fine-grained types (group I and II) of the Allende inclusions. These data in combination with other data suggest that the minerals in the coarse-grained inclusions (group I) crystallized in a closed system with respect to refractory elements although a totally molten stage is precluded. The data also indicate that fine-grained (group II) inclusions were formed by condensation from a super-cooled nebular gas; REE-rich clinopyroxene and spinel were formed earlier than REE-poor sodalite and nepheline. In addition, pre-existing Mg isotope anomalies in the coarse-grained inclusions must have been erased during the heating stage.

Nagasawa, H.↗

Chemistry of Apollo 12 mare basalts - Magma types and fractionation processes

Major and trace element data for a large suite of petrographically diverse Apollo 12 mare basalts are presented, and magma types sampled at the Apollo 12 site are characterized. The data confirm earlier classifications of the basalts into olivine, pigeonite, ilmenite, and feldspathic basalts. The olivine and pigeonite basalts are shown to be comagnetic and related by olivine fractionation. The other types, which differ in trace element and isotopic characteristics, are derived from different sources within the lunar interior. The spatial relations between the main basalt types are discussed in terms of local cratering events, and it is suggested that the younger ilmenite basalts overlie the olivine-pigeonite basalts. The role of olivine-dominated near-surface crystal fractionation in causing chemical variation is examined, and a relation between inferred cooling rate and the position of a sample in the fractionation sequence is determined.

Rhodes, J. M.↗

Compositional dispersions in lunar and terrestrial basalts

The dispersions in composition observed among samples of terrestrial basalts with known field relationships are compared with those of various subgroups of lunar mare basalts. The comparison indicates that there are no substantial reasons based on trace-element data to require that large numbers of different basalts were sampled at each Apollo site. The Apollo 15 olivine and quartz normative basalts and the Apollo 12 ilmenite and olivine basalts show compositional variations which are no more pronounced than those found within single terrestrial flows, whose inhomogeneity in horizontal section has been demonstrated. The inhomogeneities of the parent rocks in the case of the Apollo 12 and 15 basalts on a scale of centimeters overshadow any differences which might exist among different general regions of the lava flows from which these samples might have derived.

Haskin, L. A.↗

Drive tube 60009 - A chemical study of magnetic separates of size fractions from five strata

Each bulk soil and both the magnetic and nonmagnetic components of the 90-150 micron and below 20 micron fractions of five soils from drive tube 60009 were analyzed. Samples were analyzed for FeO, Na2O, Sc, Cr, Co, Ni, Hf, Ta, Th, La, Ce, Sm, Eu, Tb, Yb, and Lu by neutron activation analysis. Several samples were fused and analyzed for major elements by electron microprobe analysis. Compositional variations are not systematically related to depth. The compositions of the five soils studied are well explained by a two-component mixing model whose end members are a submature Apollo 16-type soil and an extremely immature anorthositic material similar to 60025. There is evidence that the anorthositic component had received a small amount of exposure before these soils were mixed. After mixing, the soils received little exposure suggesting mixing and deposition on a rapid time scale.

Blanchard, D. P.↗

Chemistry, classification, and petrogenesis of Apollo 17 mare basalts

Major- and trace-element data is presented for a large number of petrographically diverse Apollo 17 basalts, and an attempt is made to evaluate what proportion of the total compositional variance can be attributed to near-surface crystal fractionation and what proportion to magma-generating processes such as partial melting and source heterogeneity. Three well-defined and self-consistent basalt types were identified on the basis of data for fine-grained, rapidly-chilled samples.

Rhodes, J. M.↗

Major and trace element chemistry of Boulder 1 at Station 2, Apollo 17

Twenty-seven samples from Boulder 1 at Station 2 are analyzed for major and trace elements by atomic absorption spectrophotometry and neutron activation analysis. Two types of matrix and several types of clast materials are characterized on the basis of their chemistry. It is shown that one matrix type is a common material at the Apollo 17 site, while the other is probably exotic to that site. The most unusual clast materials found are coarse norite (an old rock no longer found in millimeter fragments at the site) and pigeonite basalt (possibly a highland volcanic rock). It is concluded that the boulder-forming process combined materials from at least two different localities or vertical strata.

Blanchard, D. P.↗

Consortium studies of matrix of light gray breccia 73215

A description is presented of the preliminary results of interdisciplinary studies of matrix samples. The significance of the 73215 studies is considered and the relationship of 73215 to other Apollo 17 highland breccias is discussed. According to a tentative hypothesis 73215 is an aggregate of fragments plus melt generated in a very large impact, possibly the Serenitatis basin-forming event. If this is correct, studies of this sample will make it possible to date the Serenitatis event and will provide an insight into the breccia-forming processes associated with such events. Studies of the clasts in the breccia will provide an opportunity to formulate a partial characterization of the preimpact source terrain. An investigation of the deep lunar crust might perhaps also be possible.

James, O. B.↗

On the origin of high-Ti mare basalts

Analyses were conducted of sixteen Apollo 17 mare basalts for alkali, alkaline-earth, and rare-earth elements, Co, and Sc. The obtained data were utilized in a study concerning the nature of the igneous processes responsible for the chemical variations among the high-Ti, low-K basalts. Estimates were obtained regarding the abundances of the large-ion, lithophile elements in the source regions for the basalts. It is shown that the source regions could plausibly have been produced by processes believed to have occurred during the early history of the moon. Attention is given to chemical variations among the Apollo 17 mare basalts, near-surface (low-pressure) crystal fractionation, partial melting, limits on the extent of partial melting, and a summary of possible events leading to formation of high-Ti mare basalts.

Shih, C.-Y.↗

Chemistry of agglutinate fractions in lunar soils

Agglutinates are aggregates of crystalline grains and lithic fragments bonded together by glass. It is thought that glassy agglutinates are formed at the upper surface of the lunar regolith by impact-related melting and welding of soil particles, in response to meteoroid and micrometeoroid bombardment. A description is presented of an investigation in which bulk soils were separated into 'agglutinate' and 'nonagglutinate' fractions. The obtained fractions were analyzed for major, minor, and trace elements. The obtained chemical data for agglutinate and nonagglutinate fractions of lunar soils indicate that agglutinitic glass is enriched in mafic and most lithophile elements relative to the bulk soils. A model involving preferential melting and assimilation of mesostasis material and mafic soil components is proposed to account for the observed chemical data. It is suggested that glassy agglutinates may form more readily in mafic soils than in more feldspathic ones. Such selectivity should be most effective between mare and highland soils, but may possibly operate on a more local scale.

Rhodes, J. M.↗

A geochemical and petrographic study of 1-2-mm fines from Apollo 17

Samples of fines less than 1-mm and 155 1-2 mm particles from several Apollo 17 sites were analyzed for Na, Sc, Cr, Mn, Fe, Co, Ni, Hf, Ta, Th, and REE. Products of comminution and construction are present in the 1-2 mm particles, and the compositions of the rock fragments clearly indicate the general chemical characteristics of their parent rock types. The likely sources of materials for the glassy particles are considered. Glasses are enriched over their parent soils in Fe, Sc, Mn, and Cr, and are relatively enriched in light REE, so that some chemical fractionation accompanies glass-forming processes. Elements were determined by instrumental neutron activation analysis.

Blanchard, D. P.↗