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Inductively coupled plasma-optical emission spectra were modeled with partial least squares regression models to quantify trace elements in uranium (20–5000 μg per g U) without chemical separations or matrix matched calibration standards.
This progress report covers work done during the second year of the 3-year proposal. During this year we resolved many issues relevant to the analytical technique developed by us for measuring trace elements in meteoritic metals. This technique was used to measure concentrations of Fe, Ni, Co, Cr, Cu, Ga, Ge, As, Mo, Ru, Rh, Pd, Sb, W, Re, Os, Ir, Pt, and Au in eight large (120 - 160 microns) metal grains from both "igneous" and "metamorphic" lithologies of the Chanuskij silicate inclusions. The first application of OUT technique to metal grains from thin sections showed some limitations. Small thickness of metal grains in the thin section limited the signal to 3-4 time-slices instead of 10- 1 1 ones in polished sections of iron meteorites studied before.
The Allende samples analyzed include seven Ca, Al-rich aggregates, ten melilite chondrules, an olivine chondrule, and two olivine-rich aggregates. The Allende meteorite has been described as a type III carbonaceous chondrite. Major element abundances were determined with the electron microprobe technique reported by Reed and Ware (1972). An MS7 spark source mass spectrometer was used for the determination of trace element abundances.
Two types of highland terrain appear to be present at the Apollo 16 landing site. The Plains Formation called Cayley is ubiquitous and blankets even those regions that were presumably a part of the mountainous Descartes Formation. The second type of terrain is that associated with the ejectae from North and South Ray craters. The stratigraphy sampled by the ejectae underlays the Cayley layer as characterized above and may permit a redefinition of Descartes Formation as that which underlays the smooth Plains deposits. These conclusions are based on the concentrations and chemical coherence between elements such as Cl-F-P2O5 and Ru-Os. The primitive lunar crust may be characterized by the type of feldspathic rocks which are enriched in trace elements, such as Cl, Br, U, Te, Ru, and Os, as found in 'rusty' rock 66095 and in 61016; other feldspathic rocks are depleted and may be of secondary origin.
The composition of recent island-arc volcanic rocks in relation to their geographic and stratigraphic relations is discussed. The differences in composition between volcanic rocks and those in continental margins are pointed out. Trace elements and major elements are shown to suggest a continuous gradational sequence from tholeiites through calc-alkaline rocks to shoshonites.
Synchrotron X-ray fluorescence spectra of unpolished iron and chondritic spheres extracted from sediments collected on the melt zone of the Greenland ice cap allow the analysis of Ni, Cu, Zn, Ga, Ge, Pb, and Se with minimum detection limits on the order of several parts per million. All detected elements are depleted relative to chondritic abundance with the exception of Pb, which shows enrichments up to a factor of 500. An apparent anticorrelation between the Ni-content and trace element concentration was observed in both types of spherules. The fractionation patterns of the iron and chondritic spheres are not complementary and consequently the two iron spheres examined in this study are unlikely to result from ejection of globules of Fe/Ni from parent chondritic micrometeoroids.
Recent models of Ca, Al-rich (CAI) inclusion petrogenesis, and the recent availability of thermodynamic data have led to the reexamination of the geochemical behavior of the refractory noble metals (RNM) and several lithophile refractory trace elements in CAI's in the context of distillation models. Here, pertinent chemical and mineralogical properties of the various classes of refractory inclusions are reviewed, and calculations of the stability of LRTE-RNM alloys and several LRTE oxides under nebular conditions are presented. The calculations, observations and experimental results are applied to a new model of the origin of refractory metal nuggets, and a specific mechanism is identified for producing Group II chemical patterns in a cold star nebula by fractionating interstellar dust at low temperature on the basis of physical differences between different populations of pre-solar grains.
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.
The Lafayette meteorite contains abundant iddingsite, a fine-grained intergrowth of smectite clay, ferrihydrite, and ionic salt minerals. Both the meteorite and iddingsite formed on Mars. Samples of iddingsite, olivine, and augite pyroxene were extracted from Lafayette and analyzed for trace elements by instrumental neutron activation. Our results are comparable to independent analyses by electron and ion microbeam methods. Abundances of most elements in the iddingsite do not covary significantly. The iddingsite is extremely rich in Hg, which is probably terrestrial contamination. For the elements Si, Al, Fe, Mn, Ni, Co, and Zn, the composition of the iddingsite is close to a mixture of approximately 50% Lafayette olivine + approximately 40% Lafayette siliceous glass + approximately 1O% water. Concordant behavior among these elements is not compatible with element fractionations between smectite and water, but the hydrous nature and petrographic setting of the iddingsite clearly suggest an aqueous origin. These inferences are both consistent, however, with deposition of the iddingsite originally as a silicate gel, which then crystallized (neoformed) nearly isochemically. The iddingsite contains significantly more magnesium than implied by the model, which may suggest that the altering solutions were rich in Mg(2+).
Although micrometeorites of cometary origin are thought to be the dominant component of interplanetary dust, it has never been possible to positively identify such micrometer-sized particles. Two such particles have been identified as definitely micrometeorites since their abundances of volatile and nonvolatile trace elements closely match those of primitive solar system material.
Mineral/melt partition coefficients have been widely used to provide insights into magmatic processes. Olivine is one of the most abundant and important minerals in the lunar mantle and mare basalts. Yet, no systematic olivine/melt partitioning data are available for lunar conditions. We report trace element partition data between host mineral olivine and its melt inclusions in lunar basalts. Equilibrium is evaluated using the Fe-Mg exchange coefficient, leading to the choice of melt inclusion-host olivine pairs in lunar basalts 12040, 12009, 15016, 15647, and 74235. Partition coefficients of 21 elements (Li, Mg, Al, Ca, Ti, V, Cr, Mn, Fe, Co, Y, Zr, Nb, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) were measured. Except for Li, V, and Cr, these elements show no significant difference in olivine-melt partitioning compared to the data for terrestrial samples. The partition coefficient of Li between olivine and melt in some lunar basalts with low Mg# (Mg# < 0.75 in olivine, or < ~0.5 in melt) is higher than published data for terrestrial * Corresponding author. Email address: youxue@umich.edu 2 samples, which is attributed to the dependence of DLi on Mg# and the lack of literature DLi data with low Mg#. The partition coefficient of V in lunar basalts is measured to be 0.17 to 0.74, significantly higher than that in terrestrial basalts (0.003 to 0.21), which can be explained by the lower oxygen fugacity in lunar basalts. The significantly higher DV can explain why V is less enriched in evolved lunar basalts than terrestrial basalts. The partition coefficient of Cr between olivine and basalt melt in the Moon is 0.11 to 0.62, which is lower than those in terrestrial settings by a factor of approximately 2. This is surprising because previous authors showed that Cr partition coefficient is independent of fO2. A quasi-thermodynamically based model is developed to correlate Cr partition coefficient to olivine and melt composition and fO2. The lower Cr partition coefficient between olivine and basalt in the Moon can lead to more Cr enrichment in the lunar magma ocean, as well as more Cr enrichment in mantle-derived basalts in the Moon. Hence, even though Cr is typically a compatible element in terrestrial basalts, it is moderately incompatible in primitive lunar basalts, with a similar degree of incompatibility as V based on partition coefficients in this work, as also evidenced by the relatively constant V/Cr ratio of 0.039 ± 0.011 in lunar basalts. The confirmation of constant V/Cr ratio is important for constraining concentrations of Cr (slightly volatile and siderophile) and V (slightly siderophile) in the bulk silicate Moon.
The accurate and precise analysis of impurities in uranium ore concentrates is an important aspect of nuclear forensics. Defensibility of analytical data requires the use of analytical reference materials as part of quality control. This report presents a compilation of the results of trace element concentration measurements of the CUP-2 Uranium Ore Concentration Standard from 11 different laboratories. Various dissolution methods, instrumental platforms, and analytical methods were employed. The resulting data set contains concentration of 66 impurities with up to 139 individual data points for each impurity. Consensus values have been assigned to each impurity following a statistical analysis of the data set.
Of six samples from boulder 1 at Station 2, four contain a unique meteoritic component, which is attributed to the Crisium projectile. The other two samples are meteorite free, igneous rocks: an unusual, alkali- and Ge-rich pigeonitic basalt, and an alkali-poor norite of unexceptional trace element chemistry.
The applicability of ion microprobe (IMP) for quantitative analysis of minor elements (Sr, Y, Zr, La, Sm, and Yb) in the major phases present in natural Ca-, Al-rich inclusions (CAIs) was investigated by comparing IMP results with those of an electron microprobe (EMP). Results on three trace-element-doped glasses indicated that it is not possible to obtain precise quantitative analysis by using IMP if there are large differences in SiO2 content between the standards used to derive the ion yields and the unknowns.
A determination is conducted of ppm-ppt levels of Co, Se, Ga, Rb, Cs, Te, Bi, Ag, In, Tl, Zn and Cd (arranged empirically in order of increasing mobility at 1000 C) by radiochemical neutron activation analysis in eight Jilin samples of known Ar-40 content and a large vein from one of these. The trace element contents of the vein do not differ markedly from those of Jilin whole-rock samples. Only Rb correlates with Ar-40, possibly due to chance. All elements but Cd are present at levels similar to thdse in H4-6 chondrites with long K/Ar age (i.e., presumably mildly shocked). These levels are low relative to those in analogous L4-6 chondrites suggesting that H chondrites formed and/or evolved under higher pre-shock temperatures than did mildly shocked L chondrites. Time-temperature conditions during shock-loading of Jilin parent material were mild relative to those in strongly shocked L chondrites, being sufficient at most only to mobilize Cd.
Ag, Au, Bi, Cd, Co, Cs, Ga, In, Rb, Sb, Se, Te, Tl, U, and Zn by RNAA are determined in two kinds of material from the Bholghati howardite: a carbonaceous chondrite clast (BH-4) that originated by primary nebular condensation/accretion processes; whole-rock samples and clasts resulting from parent-body processes, especially igneous differentiation. Trace element contents in Bholghati whole-rock (matrix) samples and/or white eucritic clasts in it are high for an achondrite, and variable. These characteristics are indicative of random condensation of volcanic emanations admixed with preexisting eucrite, diogenite, and howardite layers in the HED parent body. Other HED samples show similar patterns, and the conclusion that these reflect extensive volcanism in an asteroidal-sized object is supported by other Consortium noble gas and cosmochronologic measurements.
The delivery of material from asteroid (101955) Bennu by NASA’s OSIRIS-REx mission provides the opportunity to investigate some of the most pristine material from the early Solar System [1]. Our team at Lawrence LivermoreNational Laboratory (LLNL) utilized the equivalent of 5.0 mg from Bennu sampleOREX-803015-100 to quantify the major and trace element contents and investigate major element isotopics (Ca, Ti, Cr, Fe, and Ni). Our 5.0 mg aliquot ofOREX-803015-100 was a subsample of dissolved homogenized material representing 20.66 mg [2]. A separate 5.0 mg aliquot was sent to ETH Zürich and is discussed in a companion abstract [3]. Before any chemical separation on our 5.0 mg aliquot, the equivalent of 0.5 mg was removed and analyzed for elemental abundances at LLNL using a ThermoScientific Element XR. Our data agree exceptionally well with those reported by[2], showing that Bennu is primitive and compositionally similar to CI chondrites, Ryugu [4], and the solar photosphere [5]. The remaining ~4.5 mg underwent purification procedures to chemically isolate and purify Ca, Ti, Cr, Fe, and Ni from one another and the sample matrix. Their isotopic compositions were measured on either the Triton TIMS (Ca) at JohnsonSpace Center in Houston, Neoma MC-ICPMS (Ti, Cr) at LLNL, or the Neptune MC-ICPMS (Fe, Ni) at LLNL. Results from the Ca, Ti, Cr, Fe, and Ni isotopic compositions suggest that Bennu is closely related to CI chondrites—consistent with conclusions from elemental composition [2] and oxygen isotopics [6]reported for Bennu. The major element isotope compositions that we will present demonstrate that Bennu likely formed in a similar region of the SolarSystem as CI chondrites and potentially at a similar time of Solar System evolution.
Studies concerning Rb-Sr isotopic relations are discussed together with abundance measurements regarding K, Rb, Sr, and Ba in Apollo 14 and 15 rocks and soils. The studies include age determination by the internal isochron technique on one basaltic rock sample from each of the two missions. In addition, total sample measurements have been made on samples of fines material from both missions. Trace element abundances and Rb-Sr systematics in the various grain size fractions of three of the fines have also been analyzed.