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At least 91 records · Page 5

Long-term changes in solar wind elemental and isotopic ratios - A comparison of two lunar ilmenites of different antiquities

The solar wind components in two lunar ilmenites are examined. The noble gas and nitrogen elemental and isotopic abundances of lunar regolith breccia sample 79035, assumed to have been exposed to solar winds more than 2 Ga ago, are analyzed using stepwise oxidation and pyrolysis. This sample is compared with the data of Frick et al. (1988) for soil sample 71501, recently exposed to solar winds. It is observed that the two elements differ in terms of xenon abundance, helium and neon isotopic rates, and He/Ar elemental ratios. It is concluded that there have been isotopic and elemental abundance changes in solar wind composition over time.

Becker, Richard H.↗

The isotopic composition of galactic cosmic-ray lithium, beryllium, and boron

The isotopes of cosmic-ray Li, Be, and B near 100 MeV per nucleon have been measured with cosmic-ray telescopes on board the IMP-7 and IMP-8 satellites during 1973 and 1974. The measured isotopic abundances provide a stringent test for models of interstellar propagation and solar modulation. It is found that the isotopic abundances can be explained using a steady-state interstellar propagation model with a 5-g/sq cm leakage mean free path. These results, taken along with Be-10 abundance measurements, indicate a longer lifetime for cosmic rays than that predicted by the usual assumption of an average interstellar density of 1 to 3 atoms per cu cm.

Garcia-Munoz, M.↗

Mass spectrometric study of the mercury isotopes in the Allende meteorite

Isotopic abundance ratios for mercury were determined by mass spectrometry in six samples of bulk material and in one sample of chondrules from the Allende meteorite. A primary purpose of the work was to attempt to verify the anomalous ratios reported for Hg-196/Hg-202 by neutron activation. Measurements were made on the mercury released at temperatures of 250, 450, 600 C, and in some cases, higher temperatures. The precision of the measurements was such that if an anomaly of the magnitude reported exists, it should have been seen. The isotopic abundance ratios for the other mercury isotopes were also measured. Within the errors of measurement these agreed with normal terrestrial values.

Nier, A. O.↗

Round-robin analysis of highly depleted lithium for Generation IV nuclear reactor applications

Lithium reference materials containing unnaturally high abundances of 7 Li are not currently available, which poses quality control problems for highly depleted lithium materials (i.e., depleted in 6 Li) required for Generation IV nuclear reactors. This study presents an interlaboratory comparison of a lithium carbonate (NIST SRM924a) containing nominally natural isotopic abundances (~92.4 % Li-7) and a highly depleted lithium hydroxide material (~99.95 % Li-7). The natural lithium isotope abundances of NIST SRM924a are confirmed, and the 6 Li/ 7 Li ratio of the lithium hydroxide ranged from 0.000399 to 0.000436 with an average of 0.000428 ± 0.000023 (2SD, n = 9). Finally, going forward this material can be used as quality control for analytical work involving highly depleted lithium.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Volume Measurements of Laser-generated Pits for in Situ Geochronology Using KArLE (Potassium-Argon Laser Experiment)

KArLE (Potassium-­‐Argon Laser Experiment) has been developed for in situ planetary geochronology using the K - Ar (potassium-­‐argon) isotope system, where material ablated by LIBS (Laser-­‐Induced Breakdown Spectroscopy) is used to calculate isotope abundances. We are determining the accuracy and precision of volume measurements of these pits using stereo and laser microscope data to better understand the ablation process for isotope abundance calculations. If a characteristic volume can be determined with sufficient accuracy and precision for specific rock types, KArLE will prove to be a useful instrument for future planetary rover missions.

French, R. A.↗

Hyperfine structure and isotope shifts of xenon measured for near-infrared transitions with Doppler-free saturated absorption spectroscopy

Hyperfine structure and isotope shifts of Xe were investigated with Doppler-free saturated absorption spectroscopy for all transitions in the 820-841 nm spectral interval. The Xe samples were commercial gases of natural isotopic abundances. The measurements were performed by employing a widely tunable narrow line Ti:sapphire laser. The hyperfine structures for 129 Xe and 131 Xe were well resolved. For the transitions with the wavelengths in vacuum near 820.860 nm and 841.150 nm also isotope shifts of the even isotopes were clearly observed. The modeling of the shapes of the observed absorption lines qualitatively reproduces experimental spectral profiles. The measured absorption peaks of the hyperfine structure and isotope shifts of Xe isotopes present characteristic spectral fingerprints for their identification. Eventually, quantitative spectral analysis will provide isotopic abundances of natural, as well as radioactive Xe gas samples.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Standard atomic weights of the elements 2021 (IUPAC Technical Report)

Following the reviews of atomic-weight determinations and other cognate data in 2015, 2017, 2019 and 2021, the IUPAC (International Union of Pure and Applied Chemistry) Commission on Isotopic Abundances and Atomic Weights (CIAAW) reports changes of standard atomic weights. The symbol A r°(E) was selected for standard atomic weight of an element to distinguish it from the atomic weight of an element E in a specific substance P, designated A r(E, P). The CIAAW has changed the values of the standard atomic weights of five elements based on recent determinations of terrestrial isotopic abundances. The standard atomic weight of argon and lead have changed to an interval to reflect that the natural variation in isotopic composition exceeds the measurement uncertainty of A r(Ar) and A r(Pb) in a specific substance. The standard atomic weights and/or the uncertainties of fourteen elements have been changed based on the Atomic Mass Evaluations 2016 and 2020 accomplished under the auspices of the International Union of Pure and Applied Physics (IUPAP). A r° of Ho, Tb, Tm and Y were changed in 2017 and again updated in 2021.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

The Sm-(146,147)-Nd-(142,143) formation interval for the lunar mantle and implications for lunar evolution

Small anomalies in the isotopic abundance of Nd-142 have been measured for two A17 high-Ti basalts, ilmenite basalt 12056, olivine-pigeonite basalt 12039, feldspathic basalt 12038, and two KREEP basalts. These anomalies correlate with Sm-147/Nd-144 for the basalt source regions as calculated from initial Nd-143/Nd-144 ratios in the basalts, and are interpreted to be from decay of Sm-146 (t sub 1/2 = 103 Ma) in distinct lunar mantle reservoirs. A three-stage model for evolution of Nd-143/Nd-144 and Nd-142/Nd-144 yields reservoir Sm-147/Nd-144 ratios which, with the Nd-142/Nd-144 ratios in the basalts, form a 'mantle isochron' giving a lunar mantle formation interval of 94+2230 Ma (2c(rho)). Calculated reservoir Sm/Nd ratios are in the range expected from some earlier models of basalt petrogenesis. The isochron value of Nd-142/Nd-144 at Sm-147/Nd-144 sub CHUR = 0.1967 is within error limits of the average Nd-142/Nd-144 measured for an L6 chondrite, an H5 chondrite, and the Orgueil carbonaceous chondrite. Evolution of Nd-143 and Nd-142 for high-Ti basalt 70135 was modeled precisely, starting from chondritic relative REE and Nd-isotopic abundances and using the initial (Sm-146/Sm-144) sub 0 ratio inferred from a previous study of angrite LEW86010 as the initial solar system value of this parameter. We infer that the initial Sm/Nd ratio in precursor lunar materials was very nearly chondritic (within approximately 8 percent) prior to lunar differentiation.

Nyquist, L. E.↗

Characterization of actinide abundances and isotopic compositions by HR-ICP-MS

In this report, we present actinide isotopic and elemental data from fallout melt glass using high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS). This is an analytical technique that requires minimal sample preparation. These data are directly compared to the results of high precision isotopic analyses and elemental assay by multi-collector (MC-) ICP-MS, which requires lengthy sample processing involving spiking and purifying aliquots of individual elements. The comparison shows broad overlap between the results of the two techniques. Thus, although the data obtained by HR-ICP-MS is of significantly lower precision, it is a viable method to obtain actinide elemental and isotopic data on a more rapid timeframe than traditional high-precision techniques.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Characterization of actinide abundances and isotopic compositions by HR-ICP-MS. Part 2: Results from actinide doping studies

Previously, we presented actinide isotopic and elemental data from fallout melt glass that was measured using high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS). Direct comparison between these measurements and ‘gold standard’ data obtained by multi-collector ICP-MS showed broad overlap, indicating that HR-ICP-MS is a potentially valuable technique for producing actinide elemental and isotopic data on a relatively rapid timescale. To test the usefulness of this technique further, we doped varying amounts of uranium certified reference materials (CRMs) into a rhyolitic rock standard to establish the effects of uranium concentration and isotopic composition on the accuracy of uranium isotopic analyses by HR-ICP-MS. This also enabled us to quantify peak tailing effects from 238 U on the measurement of 239 Pu and 237 Np, which in turn allows us to constrain correction factors based on measured 237 Np/ 238 U and 239 Pu/ 238 U ratios. A second doping study involved the addition of a mixed actinide standard into three samples with different matrix compositions (termed soil, city, and seawater) to assess whether sample chemistry affects the accuracy and precision of these analyses. Results suggest that this is not the case. Systematic offsets were not observed in elemental or isotopic data derived from the three matrix samples. Results indicate that useful actinide isotopic data can be obtained from whole rock solutions by HR-ICP-MS. Our findings also have implications for solid sampling techniques such as laser ablation ICP-MS, which do not require sample dissolution.

38 RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEA↗

Nitrogen abundances and isotopic compositions in lunar samples

Isotopic analyses were carried out on soil separates as well as on bulk samples. Analyses of nitrogen fractions obtained by step-wise heating of the separates were also conducted. It was also attempted to obtain a value for the isotopic composition of indigenous lunar nitrogen from analyses of igneous rock samples. Several breccias were also analyzed for their nitrogen isotope ratios. The significance of the obtained results is discussed. Several lines of evidence point to the conclusion that the isotope ratio of the nitrogen being implanted into the lunar regolith has increased by some 15% over a period of at least 450 million years and possibly as long as 3,700 million years or more. This may be the result of changes in the nitrogen isotope ratio of the solar wind with time, or it may be due to outgassing and subsequent reimplantation of an isotopically light indigenous lunar nitrogen from the lunar interior in the early history of the moon.

Becker, R. H.↗

The isotopic composition of helium at high rigidities

The isotopic abundance distribution of the cosmic radiation at energies beyond 1 GeV/AMU can at the present time be determined only with the geomagnetic method. A balloon-borne instrument was flown for 12 hours near the geomagnetic equator to measure the relative abundance of the helium isotopes He-3 and He-4 around 12 GV rigidity. The sharp rigidity cut-off at equatorial latitudes permitted separation of the two isotopes using a high-resolution-gas Cerenkov counter. The experiment thus confirms the predicted sharp cut-off at those latitudes and demonstrates the potential for isotopic separation of other elements, once flights of longer duration can be made.

Jordan, S. P.↗

Thermal spectroscopy of Neptune - The stratospheric temperature, hydrocarbon abundances, and isotopic ratios

NASA-IRTF observations of Neptune's disk-averaged spectrum are presently used, in conjunction with a lower-resolution spectrum, to furnish a more reliable absolute intensity calibration of portions of Neptune's disk-averaged spectrum. The temperature profile adopted is consistent with the size and shape of the H2 J = 3-1 quadrupole feature detected in the emission. High-resolution measurements of (C-13C-12)H6 and (C-12)2H6 imply C-12/C-13 of 78 +/- 26; this is consistent with solar and telluric values.

Orton, Glenn S.↗

Abundance and Isotopic Composition of Gases in the Martian Atmosphere: First Results from the Mars Curiosity Rover

Repeated measurements of the composition of the Mars atmosphere from Curiosity Rover yield a (40)Ar/N2 ratio 1.7 times greater and the (40)Ar/(36)Ar ratio 1.6 times smaller than the Viking Lander values in 1976. The unexpected change in (40)Ar/N2 ratio probably results from different instrument characteristics although we cannot yet rule out some unknown atmospheric process. The new (40)Ar/(36)Ar ratio is more aligned with Martian meteoritic values. Besides Ar and N2 the Sample Analysis at Mars instrument suite on the Curiosity Rover has measured the other principal components of the atmosphere and the isotopes. The resulting volume mixing ratios are: CO2 0.960(+/- 0.007); (40)Ar 0.0193(+/- 0.0001); N2 0.0189(+/- 0.0003); O2 1.45(+/- 0.09) x 10(exp -3); and CO 5.45(+/- 3.62) x 10(exp 4); and the isotopes (40)Ar/(36)Ar 1.9(+/- 0.3) x 10(exp 3), and delta (13)C and delta (18)O from CO2 that are both several tens of per mil more positive than the terrestrial averages. Heavy isotope enrichments support the hypothesis of large atmospheric loss. Moreover, the data are consistent with values measured in Martian meteorites, providing additional strong support for a Martian origin for these rocks.

Results from Curiosity↗

The Abundance and Isotopic Signature of Chlorine in UrKREEP: Implications for the Early Degassing of the Moon

Initally, the elevated delta-37 Cl values of lunar materials were attributed to volcanic degassing[1]. However, chlorine isotope ratios of apatite in lunarmare basalts appear to reflect mixing between two reservoirs.One component, with elevated delta-37 Cl is greater than or equal to + (25%) ([2] may represent the urKREEP--the final product of the crystallization of the lunar magma ocean. The second component, with delta-37 Cl is approximately (0%), is inferred to represent either a mare basalt reservoir or meteoritic materials. The idea that high delta-37 Cl is related to urKREEP suggest a global enrichment that occurred earlier in the lunar history [2,3]. Here we test this urKREEP-mixing hypothesis more rigorously, and report the observed limits of the model. We then use the results to calculate the Cl content of the urKREEP component and use those results to update estimates of the bulk Cl content of the Moon. This allows us to speculate on the mechanisms of loss of Cl from the lunar magma ocean.

Boyce, J. W.↗