The iodine-plutonium-xenon age of the Moon-Earth system revisited

From iodine-plutonium-xenon isotope systematics, we re-evaluate time constraints on the early evolution of the Earth-atmosphere system and, by inference, on the Moon-forming event. Two extinct radioactivites (129I, T1/2 = 15.6 Ma, and 244Pu, T1/2 = 80 Ma) have produced radiogenic 129Xe and fissiogenic 131-136Xe, respectively, within the Earth, which related isotope fingerprints are seen in the compositions of mantle and atmospheric Xe. Recent studies of Archean rocks suggest that xenon atoms have been lost from the Earth's atmosphere and isotopically fractionated during long periods of geological time, until at least the end of the Archean eon. Here we build a model that takes into account these results. Correction for Xe loss permits to compute new closure ages for the Earth's atmosphere that are in agreement with those computed for mantle Xe. The minimum Xe formation interval for the Earth- atmosphere is 40 (-10+20) Ma after start of solar system formation, which may also date the Moon-forming impact.Comment: 27 pages, 3 figures, 2 table

La BLSH à l'ère du Web 2.0

La présentation Powerpoint originale a été convertie au format PDF afin d'alléger la taille du fichier mis en ligne.Document produit lors de la journée hors-les-murs réunissant les bibliothécaires de la BLSH au Musée d'art contemporain de Montréal (mai 2008). Cette rencontre a été organisée dans le but de donner suite à la journée de réflexion des bibliothécaires intitulée Usagers 2.0 ? ou comment répondre adéquatement aux nouveaux comportements informationnels de notre clientèle (décembre 2007). Le document consiste en une présentation d'une gamme d'applications du Web 2.0 pouvant être utiles en bibliothèque universitaire. Des exemples concrets sont donnés pour chacune des applications

Origin and significance of cosmogenic signatures in vesicles of lunar basalt 15016

Lunar basalt 15016 (~3.3 Ga) is among the most vesicular (50% by volume) basalts recovered by the Apollo missions. We investigated the possible occurrence of indigenous lunar nitrogen and noble gases trapped in vesicles within basalt 15016, by crushing several cm‐sized chips. Matrix/mineral gases were also extracted from crush residues by fusion with a CO_2 laser. No magmatic/primordial component could be identified; all isotope compositions, including those of vesicles, pointed to a cosmogenic origin. We found that vesicles contained ~0.2%, ~0.02%, ~0.002%, and ~0.02% of the total amount of cosmogenic ^(21)Ne, ^(38)Ar, ^(83)Kr, and ^(126)Xe, respectively, produced over the basalt's 300 Myr of exposure. Diffusion/recoil of cosmogenic isotopes from the basaltic matrix/minerals to intergrain joints and vesicles is discussed. The enhanced proportion of cosmogenic Xe isotopes relative to Kr detected in vesicles could be the result of kinetic fractionation, through which preferential retention of Xe isotopes over Kr within vesicles might have occurred during diffusion from the vesicle volume to the outer space through microleaks. This study suggests that cosmogenic loss, known to be significant for ^3He and ^(21)Ne, and to a lesser extent for ^(36)Ar (Signer et al. 1977), also occurs to a negligible extent for the heaviest noble gases Kr and Xe

Salinity of the Archaean oceans from analysis of fluid inclusions in quartz

Fluids trapped in inclusions in well-characterized Archaean hydrothermal quartz crystals were analyzed by the extended argon–argon method, which permits the simultaneous measurement of chlorine and potassium concentrations. Argon and nitrogen isotopic compositions of the trapped fluids were also determined by static mass spectrometry. Fluids were extracted by stepwise crushing of quartz samples from North Pole (NW Australia) and Barberton (South Africa) 3.5–3.0-Ga-old greenstone belts. The data indicate that fluids are a mixture of a low salinity end-member, regarded as the Archaean oceanic water, and several hydrothermal end-members rich in Cl, K, N, and radiogenic parentless ^(40)Ar. The low Cl–K end-member suggests that the salinity of the Archaean oceans was comparable to the modern one, and that the potassium content of the Archaean oceans was lower than at present by about 40%. A constant salinity of the oceans through time has important implications for the stabilization of the continental crust and for the habitability of the ancient Earth

Comparison of near-interface traps in Al2_2O3_3/4H-SiC and Al2_2O3_3/SiO2_2/4H-SiC structures

Aluminum oxide (Al2O3) has been grown by atomic layer deposition on n-type 4H-SiC with and without a thin silicon dioxide (SiO2) intermediate layer. By means of Capacitance Voltage and Thermal Dielectric Relaxation Current measurements, the interface properties have been investigated. Whereas for the samples with an interfacial SiO2 layer the highest near-interface trap density is found at 0.3 eV below the conduction band edge, Ec, the samples with only the Al2O3 dielectric exhibit a nearly trap free region close to Ec. For the Al2O3/SiC interface, the highest trap density appears between 0.4 to 0.6 eV below Ec. The results indicate the possibility for SiC-based MOSFETs with Al2O3 as the gate dielectric layer in future high performance devices.Comment: 3 figures. Applied Physics Letters, accepted for publicatio

A comprehensive study of noble gases and nitrogen in Hypatia, a diamond-rich pebble from SW Egypt

This is a follow-up study of a work by Kramers et al. (2013) on an unusual diamond-rich rock found in the SW side of the Libyan Desert Glass strewn field. This pebble, called Hypatia, is composed of almost pure carbon. Transmission Electron Microscopy and X-ray diffraction results reveal that Hypatia is made of defect-rich diamond containing lonsdaleite and deformation bands. These characteristics are compatible with an impact origin on Earth and/or in space. We analyzed concentrations and isotopic compositions of all five noble gases and nitrogen in several mg sized Hypatia samples. These data confirm that Hypatia is extra-terrestrial. The sample is rich in trapped noble gases with an isotopic composition close to the meteoritic Q component. 40Ar/36Ar ratios in individual steps are as low as 0.4. Concentrations of cosmic-ray produced 21Ne correspond to a nominal cosmic-ray exposure age of ca. 0.1 Myr if produced in a typical m-sized meteoroid. Such an atypically low nominal exposure age suggests high shielding in a considerably larger body. In addition to the Xe-Q composition, an excess of radiogenic 129Xe (from the decay of extinct 129I) is observed (129Xe/132Xe = 1.18 +/- 0.03). Two N components are present, an isotopically heavy component ({\delta}15N = +20 permil) released at low temp. and a major light component ({\delta}15N = -110 permil) at higher temp. This disequilibrium in N suggests that the diamonds in Hypatia were formed in space. Our data are broadly consistent with concentrations and isotopic compositions of noble gases in at least three different types of carbon-rich meteoritic materials. However, Hypatia does not seem to be related to any of these materials, but may have sampled a similar cosmochemical reservoir. Our study does not confirm the presence of exotic noble gases that led Kramers et al. to propose that Hypatia is a remnant of a comet that impacted the Earth

Stepwise heating of lunar anorthosites 60025, 60215, 65315 possibly reveals an indigenous noble gas component on the Moon

Despite extensive effort during the last four decades, no clear signature of a lunar indigenous noble gas component has been found. In order to further investigate the possible occurrence of indigenous volatiles in the Moon, we have re-analyzed the noble gas and nitrogen isotopic compositions in three anorthosite samples. Lunar anorthosites 60025, 60215 and 65315 have the lowest exposure duration (∼2 Ma) among Apollo samples and consequently contain only limited cosmogenic (e.g. ^(124,126)Xe) and solar wind (SW) noble gases. Furthermore, anorthosites have negligible contributions of fissiogenic Xe isotopes because of their very low Pu and U contents. As observed in previous studies (Lightner and Marti, 1974; Leich and Niemeyer, 1975), lunar anorthosite Xe presents an isotopic composition very close to that of terrestrial atmospheric Xe, previously attributed to “anomalous adsorption” of terrestrial Xe after sample return. The presumed atmospheric Xe contamination can only be removed by heating the samples at medium to high temperatures under vacuum, and is therefore different from common adsorption. To test this hypothesis, we monitored the adsorption of Xe onto lunar anorthositic powder using infrared reflectance spectroscopy. A clear shift in the anorthosite IR absorbance peaks is detected when comparing the IR absorbance spectra of the lunar anorthositic powder before and after exposure to a neutral Xe-rich atmosphere. This observation accounts for the chemical bonding (chemisorption) of Xe onto anorthosite, which is stronger than the common physical bonding (physisorption) and could account for the anomalous adsorption of Xe onto lunar samples. Our high precision Xe isotope analyses show slight mass fractionation patterns across ^(128–136)Xe isotopes with systematic deficits in the heavy Xe isotopes (mostly ^(136)Xe and marginally ^(134)Xe) that have not previously been observed. This composition could be the result of mixing between an irreversibly adsorbed terrestrial contaminant that is mostly released at high temperature and an additional signature. Solar Wind (SW) Xe contents, estimated from SW-Ne and SW-Ar concentrations and SW-Ne/Ar/Xe elemental ratios, do not support SW as the additional contribution. Using a χ^2 test, the latter is best accounted for by cometary Xe as measured in the coma of Comet 67P/Churyumov-Gerasimenko (Marty et al., 2017) or by the primordial U-Xe composition inferred to be the precursor of atmospheric Xe (Pepin, 1994; Avice et al., 2017). It could have been contributed to the lunar budget by volatile-rich bodies that participated to the building of the terrestrial atmosphere inventory (Marty et al., 2017)

Multiple carriers of Q noble gases in primitive meteorites

The main carrier of primordial heavy noble gases in chondrites is thought to be an organic phase, known as phase Q, whose precise characterization has resisted decades of investigation. Indirect techniques have revealed that phase Q might be composed of two subphases, one of them associated with sulfide. Here we provide experimental evidence that noble gases trapped within meteoritic sulfides present chemically- and thermally-driven behavior patterns that are similar to Q-gases. We therefore suggest that phase Q is likely composed of two subcomponents: carbonaceous phases and sulfides. In situ decay of iodine at concentrations levels consistent with those reported for meteoritic sulfides can reproduce the 129Xe excess observed for Q-gases relative to fractionated Solar Wind. We suggest that the Q-bearing sulfides formed at high temperature and could have recorded the conditions that prevailed in the chondrule-forming region(s)