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Evaluating Crustal Contamination Effects On The Lithophile Trace Element Budget Of Shergottites, NWA 856 As A Test Case

The issue of whether crustal contamination has affected the lithophile trace element budget of shergottites has been a point of contention for decades. The evaluation has focused on the enriched shergottite compositions as an outcome of crustal contamination of mantle-derived parent magmas or, alternatively, the compositions of these stones reflect an incompatible trace element (ITE) enriched mantle source.

Brandon, A. D.↗

The simultaneous determination of 20 trace elements in terrestrial, lunar and meteoritic material by radiochemical neutron activation analysis

A radiochemical neutron activation method has been developed and applied to determine the content of 20 trace elements (Ag, Au, Bi, Br, Cd, Co, Cs, Cu, Ga, Ge, In, Ir, Ni, Rb, Re, Sb, Te, Tl, and Zn) in 45 terrestrial, 230 lunar, and 70 meteoritic samples. Results obtained for the U.S.G.S. standard basalt BCR-1 indicate that the inherent precision for most elements is 10% or better. The values obtained for the trace elements investigated are compared to those previously reported in the literature. Data for Type I carbonaceous chondrites show their compositions to be far more uniform than previously supposed. The values obtained for several elements represent significant revisions in the accepted cosmic abundances. These new values include: Zn, 1250; Cd, 1.51; and Ir, 0.72 atoms/million Si atoms. Further results have provided insight into the meteoritic material and accretion of the moon, and give evidence of lunar highland vulcanism.

Keays, R. R.↗

Chemical studies of L chondrites. III - Mobile trace elements and Ar-40/Ar-39 ages

Radiochemical neutron activation analysis has been used to determine the content of the mobile trace elements Ag, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Se, Te, Tl, and Zn, in L4-6 chondrites with undisturbed Ar-40 release patterns or patterns showing some 4.4-4.6 Gyr plateau disturbance that indicates some shock-induced loss. The mean concentrations are significantly lower in 16 chondrites with disturbed patterns than in 4 with undisturbed ones, consistent with shock-induced mobilization. Significantly lower mean concentrations of nearly all trace elements in 26 strongly shocked chondrites than in 14 mildly shocked ones indicate loss in shock-formed FeS-Fe eutectic and/or by means of vaporization during cooling of shock-heated collisional debris.

Huston, T. J.↗

Evaluation of Compton suppression for enhancing trace element identification in neutron activation analysis of reference materials

Neutron activation analysis (NAA) is a powerful technique for identifying and quantifying trace elements in materials. However, challenges such as high dead times, spectral interferences, and high Compton continuum often arise. This study employs a Compton suppression system (CSS) to enhance NAA sensitivity by reducing the Compton continuum, thereby improving the peak-to-Compton ratio. National Institute of Standards and Technology certified reference materials 1632d, 1633c, and Canadian National Research Council TORT-1 were irradiated in a thermal and epithermal neutron flux under various irradiation, decay and counting times and analyzed using high-resolution gamma-ray spectroscopy with and without Compton suppression. The reduction factor was calculated to evaluate the effectiveness of the CSS, demonstrating significant background reduction and improved detection limits for trace elements. Additional experiments with a 137Cs point source demonstrated the impact of detector-source geometry on system performance, showing a decrease in the reduction factor as the source was moved further from the NaI detector. An optimum distance between the source and HPGe detector was observed, yielding the highest peak-to-Compton ratio. The results highlight the CSS's ability to minimize spectral interference and enhance elemental identification.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

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.↗

Rare earths and other trace elements in Apollo 14 samples.

REE and other trace elements have been determined in igneous rocks 14053, 14072, and 14310, in breccias 14063 and 14313, and in fines 14163. All materials analyzed have typical depletions of Eu except for feldspar fragments from the breccias and igneous fragments from 14063. Igneous rocks 14072 and 14053 have REE concentrations very similar to Apollo 12 basalts; 14310 has the highest REE concentrations yet observed for a large fragment of lunar basalt. The effects of crystallization of a basaltic liquid as a closed system on the concentrations of Sm and Eu in feldspar are considered. Small anorthositic fragments may have originated by simple crystallization from very highly differentiated basalt (KREEP) or by closed-system crystallization in a less differentiated starting material. Application of independent models of igneous differentiation to Sm and Eu in massive anorthosite 15415 and to Sm and Eu in lunar basalts suggests a common starting material with a ratio of concentrations of Sm and Eu about the same as that in chondrites and with concentrations of those elements about 15 times enriched over chondrites.

Helmke, P. A.↗

Major impacts on the moon - Characterization from trace elements in Apollo 12 and 14 samples.

Seventeen trace elements have been determined by neutron activation analysis in 33 lunar samples from Apollo 14, 5 from Apollo 12, and 2 from Luna 16. Apollo 14 soils and breccias contain at least two, and possibly three, ancient meteoritic components of unusual composition, probably derived from the Imbrian and Serenitatis impacts, and mixed planetesimal debris from the pre-Imbrian regolith. These components have a lower ratio of volatiles to siderophiles than any known class of chondrites. They also have Ir/Au, Ge/Au ratios outside the range for most iron meteorites, except groups IVA and possibly IIIA. One of these components, of very low Ir/Au, Re/Au ratio, occurs in light norites, 14321 microbreccias, and KREEP separates from 12033 soil. Another is found in dark norites, glasses, and several other Apollo 14 samples, as well as rock 12013 and Apollo 11 anorthosite. From these compositional clues it appears that the Imbrian body and the pre-Imbrian planetesimals, like the earth, were relatively rich in iron, but depleted in volatiles. Such a composition is consistent with the Imbrian body originating as an earth-crossing planetesimal.

Morgan, J. W.↗

Trace elements in rims and interiors of Chainpur chondrules

Trace elements were measured in the rims and interiors of nine chondrules separated from the Chainpur LL-3 chondrite. Whole rock samples of Chainpur and samples of separated rims were also measured. Chondrule rims are moderately enriched in siderophile and volatile elements relative to the chondrule interiors. The enriched volatile elements include the lithophilic volatile element Zn. The moderate enrichment of volatiles in chondrule rims and the lack of severe depletion in chondrules can account for the complete volatile inventory in Chainpur. These results support a three-component model of chondrite formation in which metal plus sulfide, chondrules plus rims and matrix silicates are mixed to form chondrites.

Wilkening, L. L.↗

Trace element composition of Luna 24 Crisium VLT basalt

The origins of the individual particles analyzed from the Luna 24 core and the information they provide on the trace-element composition of Mare Crisium basalt are considered. Previous analyses of several Luna 24 soil fragments are reviewed. It is concluded that: (1) the average trace-element concentrations for 12 VLT basalt fragments are the best available estimates for bulk samples of Crisium VLT basalt; (2) there is weak evidence that the average Crisium basalt might have a small positive Eu anomaly relative to chondritic matter; (3) the soils contain components from sources other than the Crisium VLT basalt; and (4) there is no convincing information in concentrations of rare-earth elements, Co, Sc, FeO, or Na2O among the analyzed fragments to indicate more than one parent basalt.

Haskin, L. A.↗

Trace elements in ocean ridge basalt glasses - Implications for fractionations during mantle evolution and petrogenesis

Seven documented and fresh glassy selvages from ocean floor basalt pillows were analyzed for trace elements including Ag, Au, Bi, Br, Ni, Pd, and Zn using radiochemical activation analysis. Glasses from DSDP leg 24, site 238 in the Indian Ocean have a trace element pattern which reflects secondary processes at a shallow depth. Chemical fractionations in petrogenesis of tholeiitic basalts indicate that (Ir, Os), Au, Pd, Ni, and Re are strongly fractionated in igneous processes; the unfractionated chondritic mantle pattern thus imposes constraints on mantle evolution models. Finally, the limited Rb/Cs fractionation in oceanic tholeiites reflects the low abundance of volatiles and hydrous silicates in normal ocean ridge basalts.

Hertogen, J.↗

Collaborative Study for Certification of Trace Elements in Uranium Ore Concentrate CRMs UCLO-1, UCHI-1, and UPER-1

Trace impurity patterns are important nuclear forensic signatures in uranium ore concentrates (UOCs) and Certified Reference Materials (CRMs) are used to validate the analysis methods employed by end users. Herein, we discuss the certification campaign for three new UOC CRMs from the National Research Council Canada: UCLO-1 (https://doi.org/10.4224/crm.2020.uclo-1), UCHI-1 (https://doi.org/10.4224/crm.2020.uchi-1), and UPER-1 (https://doi.org/10.4224/crm.2020.uper-1). This study involved 15 laboratories from 10 countries, using sector-field and (triple) quadrupole inductively-coupled plasma mass spectrometry to analyze 64 trace element impurities. We discuss the importance of the acids used for sample digestion, difficulties analyzing in a high uranium matrix, and data combination and uncertainty evaluation for this large dataset.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

Minor and trace elements in some meteoritic minerals.

Despite the information available (Mason, 1971) on trace elements in different types of meteorites, relatively little is known about the distribution of these elements among the individual mineral phases. The mineral phases including olivine, orthopyroxene, clinipyroxene, troilite, nickel-iron, plagioclase, chromite, and the phosphates were separated from several meteorites. The purified minerals were analyzed for trace and minor elements by spark source mass spectrometry and instrumental neutron activation analysis. The elements are classified as siderophile, lithophile, and chalcophile.

Allen, R. O., Jr.↗

An experimental study of trace element partitioning between perovskite, hibonite and melt: Equilibrium values

The presence of perovskite (CATiO3) and hibonite (Ca Al12O19) within different regions of Calcium-, Aluminum-rich Inclusions (CAI) and the trace element concentrations of these minerals in each circumstance, constrain models of precursor formation, nebular condensation, the thermal history of inclusions with relict perovskite and hibonite, and the formation of the Wark-Lovering rim. At present mineral/melt partition coefficient data for hibonite are limited to a few elements in simple experimental systems, or to those derived from hibonite-glass pairs in hibonite/glass microspherules. Similarly, there is only limited data on perovskite D that are applicable to meteorite compositions. Apart from the importance of partitioning studies to meteorite research, D values also are invaluable in the development of thermodynamic models, especially when data is available for a large number of elements that have different ionic charge and radii. In addition, study of the effect of rapid cooling on partitioning is crucial to our understanding of meteorite inclusions. To expand our knowledge of mineral/melt D for perovskite and hibonite, a study was instituted where D values are obtained in both equilibrium and dynamic cooling experiments. As an initial phase of this study mineral/melt D was measured for major elements (Ca, Mg, Al, Ti, and Si), 15 rare earth elements (La-Lu) and 8 other elements (Ba, Sr, U, Th, Nb, Zr, Hf, and Ge) in perovskite and hibonite grown under equilibrium conditions, in bulk compositions that are respectively similar to Compact Type A (CTA) CAI and to a hibonite/glass microspherule. Experimental mixes were doped with REE at 20-50x chondritic (ch) abundances, Ba at 50 ppm, Sr, Hf, Nb, and Zr at 100 ppm and, U and Th at 200 ppm. Trace element abundances were measured with the PANURGE ion microprobe. Major element compositions were obtained by electron microprobe analysis.

Kennedy, A. K.↗

Volatile/mobile trace elements in Karoonda /C4/ chondrite

Concentrations of ten volatile/mobile trace elements and of nonvolatile Co in the Karoonda (C4) meteorite were determined, and the atomic abundances relative to C1 are compared with values for the Murchison (C2) and Allende (C3) meteorites. Empirical Bi, In, and Tl data for Karoonda and heated Allende and Murchison are compared with theoretical curves for condensation from a gas of cosmic composition at low pressures. It is suggested that Karoonda might derive from low-temperature open-system metamorphism of pristine C3-like material.

Matza, S. D.↗