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Chyi, L. L.

Publications and source records attributed to Chyi, L. L..

The distribution of zirconium and hafnium in terrestrial rocks, meteorites and the moon

It is shown that Zr and Hf are not always fractionated in terrestrial igneous differentiation or regional metamorphism. Data do support a Zr-Hf fractionation in the differentiation of the alkali olivine magma at St. Helena Island. A strong Zr-Hf fractionation exists among lunar rocks and minerals. Ilmenite is an excellent concentrator of Zr and Hf and always exhibits high Zr/Hf ratios. Chondritic meteorites exhibit rather uniform Zr abundances and Zr/Hf ratios but a distinct Zr-Hf fractionation is observed among the eucrite and diogenite achondrites.

Ehmann, W. D.↗

Zirconium and hafnium in meteorites

The abundances of zirconium and hafnium have been determined in nine stony meteorites by a new, precise neutron-activation technique. The Zr/Hf abundance ratios for the chondrites vary in a rather narrow range, consistent with previously published observations from our group. Replicate analyses of new, carefully selected clean interior samples of the Cl chondrite Orgueil yield mean zirconium and hafnium abundances of 5.2 and 0.10 ppm, respectively. These abundances are lower than we reported earlier for two Cl chondrite samples which we now suspect may have suffered contamination. The new Cl zirconium and hafnium abundances are in closer agreement with predictions based on theories of nucleosynthesis than the earlier data.

Ehmann, W. D.↗

Abundances of the group IVB elements, Ti, Zr, and Hf and implications of their ratios in lunar materials

New data on Zr and Hf abundances in samples from recent Apollo missions and a few from earlier missions are presented. The data confirm our previous suggestion of a modest Zr-Hf fractionation among lunar rock types. The four major lunar rock types can be readily distinguished, based on Zr and Hf abundances and Zr/Hf mass ratios. Mare basalts exhibit mean Zr abundances ranging from 111 ppm for Apollo 15 to 534 ppm for Apollo 11 and low Zr/Hf mass ratios ranging from 34 to 39. KREEP basalts are characterized by very high Zr contents (mean = 1380 ppm Zr) and high Zr/Hf ratio of 47. Anorthosites exhibit extremely low Zr and Hf contents and possibly very low Zr/Hf ratios. Arguments that the fractionation may be partly due to the presence of Zr(3+) in lunar magmas while Hf remains as Hf(4+) are presented. These data for Zr and Hf together with data for Ti recently obtained on the same samples in our laboratory are discussed in support of a modified two-stage lunar crustal evolution model.

Ehmann, W. D.↗

Zirconium and hafnium abundances in some lunar materials and implications of their ratios

A new rapid and precise analytical procedure for Zr and Hf has been applied to the study of lunar materials. The results indicate that the Zr/Hf ratios in lunar materials vary in a narrow range from 36.6 to 51.3 while their respective contents vary by a factor of 40. There is a strong Zr, Hf, and major element correlation. This correlation and the Zr and Hf systematics suggest that lunar materials fall into two groups. One group characterized by high Zr and Hf contents and higher Zr/Hf ratios corresponds to materials with a high KREEP content; the other characterized by low Zr and Hf contents and lower Zr/Hf ratios corresponds to materials with high Ti, Fe, Mn, and Mg contents. We believe that the modest Zr and Hf fractionation we observe is related to the extent of stabilization of the metals in the early titanium minerals and a charge disparity under extremely reduced conditions in which Zr exists as 3+, while Hf remains as 4+.

Chyi, L. L.↗

Elemental abundances in the Havero meteorite.

Abundances of 15 major, minor, and trace elements have been determined in powders and interior chips derived from the Havero ureilite. The values are in close agreement with mean values for other ureilites, as reported in the literature. The powdered samples exhibited slightly higher abundances of O and Si than the interior chips. It is suggested that this may be due to alteration of the samples during the powdering process.

Gillum, D. E.↗