265 research outputs found
Non-traditional stable isotopes Reviews in mineralogy and geochemistry./ editors, Fang-Zhen Teng, James Watkins, Nicolas Dauphas.
In English.Includes bibliographical references.The development of multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS) makes it possible to precisely measure non-traditional stable isotopes. This volume reviews the current status of non-traditional isotope geochemistry from analytical, theoretical, and experimental approaches to analysis of natural samples. In particular, important applications to cosmochemistry, high-temperature geochemistry, low-temperature geochemistry, and geobiology are discussed. This volume provides the most comprehensive review on non-traditional isotope geochemistry for students and researchers who are interested in both the theory and applications of non-traditional stable isotope geochemistry.Table of Contents ; 1. Non-Traditional Stable Isotopes: Retrospective and Prospective ; 2. Equilibrium Fractionation of Non-traditional Isotopes: a Molecular Modeling Perspective ; 3. Equilibrium Fractionation of Non-traditional Stable Isotopes: an Experimental Perspective.4. Kinetic Fractionation of Non-Traditional Stable Isotopes by Diffusion and Crystal Growth Reactions 5. In Situ Analysis of Non-Traditional Isotopes by SIMS and LA-MC-ICP-MS: Key Aspects and the Example of Mg Isotopes in Olivines and Silicate Glasses ; 6. Lithium Isotope Geochemistry.7. Magnesium Isotope Geochemistry 8. Silicon Isotope Geochemistry ; 9. Chlorine Isotope Geochemistry ; 10. Chromium Isotope Geochemistry ; 11. Iron Isotope Systematics ; 12. The Isotope Geochemistry of Ni ; 13. The Isotope Geochemistry of Zinc and Copper.14. Germanium Isotope Geochemistry 15. Selenium Isotopes as a Biogeochemical Proxy in Deep Time ; 16. Good Golly, Why Moly? The Stable Isotope Geochemistry of Molybdenum ; 17. Recent Developments in Mercury Stable Isotope Analysis.18. Investigation and Application of Thallium Isotope Fractionation 19. Uranium Isotope Fractionation ; 20. Medical Applications of Isotope Metallomics.1 online resource (902 pages
The chemistry of fine-grained terrigenous sediments reveals a chemically evolved Paleoarchean emerged crust
The nature of the rocks exposed to weathering and erosion on continents exerts an important control on weathering feedbacks and the supply of nutrients to the oceans. It also reflects the prevailing tectonic regime responsible for the formation of continents. How the chemical and lithological compositions of the continents evolved through time is, however, still a matter of debate. We use an extensive compilation of terrigenous sediment compositions to better constrain the nature of rocks at the surface of continents at 3.25 Gyr and 250 Myr ago. Specifically, we use geochemical ratios that are sensitive indicators of komatiite, mafic, and felsic rocks in the provenance of the sediments. Our results show that the average Al2O3/TiO2 ratio of fine-grained terrigenous sediments decreased slightly over time from 26.2 ± 1.3 in the Archean to 22.1 ± 1.1 (2SE) in the Phanerozoic. In contrast, in the same time interval, the average Zr/TiO2 ratio stayed nearly constant at ∼245. Considering the distinct behaviors of Al, Ti and Zr during sedimentary processes, we find that hydrodynamic mineral sorting had a minor effect on the chemical composition of Archean fine-grained sediments, but could have been more effective during periods of supercontinents. We show that the compositions of Phanerozoic sediments (Al2O3/TiO2, Zr/TiO2, La/Sc, Th/Sc, Ni/Co, Cr/Sc) are best explained with igneous rocks at the surface of continents consisting of 76 ± 8 wt% felsic, 14 ± 6 wt% Arc-basalts and 10 ± 2 wt% within-plate basalts, most likely in the form of continental flood basalts. Applying the same mass-balance calculations to the Paleoarchean suggests continental landmasses with 65 ± 7 wt% felsic, 25 ± 6 wt% mafic and 11 ± 3 wt% ultramafic rocks (all 2SE), likely in the form of komatiites. The presence of volumetrically abundant felsic rocks at the surface of continents (as evident from the sediment record) as well as at mid-crustal levels (as evident from presently exposed igneous rock record) in Paleoarchean cratons is currently best explained with the onset of subduction magmatism before 3.25 Gyr
Lunar soil record of atmosphere loss over eons
The Moon has a tenuous atmosphere produced by space weathering. The short-lived nature of the atoms surrounding the Moon necessitates continuous replenishment from lunar regolith through mechanisms such as micrometeorite impacts, ion sputtering, and photon-stimulated desorption. Despite advances, previous remote sensing and space mission data have not conclusively disentangled the contributions of these processes. Using high-precision potassium (K) and rubidium (Rb) isotopic analyses of lunar soils from the Apollo missions, our study sheds light on the lunar surface-atmosphere evolution over billions of years. The observed correlation between K and Rb isotopic ratios (δ 87Rb = 0.17 δ 41K) indicates that, over long timescales, micrometeorite impact vaporization is the primary source of atoms in the lunar atmosphere
Chemical evolution of the continental crust from a data-driven inversion of terrigenous sediment compositions
The nature of emerged continents through time is highly debated. Several studies relying on trace element data concluded that the Archaean crust was predominantly mafic, while Ti isotope systematics point to an Archaean crust that was predominantly felsic. Here, we resolve the inconsistency between these two approaches by applying a novel statistical method to a compilation of published elemental concentrations in terrigenous sediments (the OrTeS database). We use a filter based on the Local Outlier Factor to reject sediment samples that have been affected by alteration processes or mineral fractionation during transport. The nature of the emerged continents is calculated using an inverse mixing model based on a Markov Chain Monte Carlo algorithm. A procedure is presented to automatically select elemental ratios that are best suited for constraining the sediment provenance. We find that for all systems that accurately reconstruct the modern-day composition of the continents, a continuous >50% felsic contribution is required to explain the composition of fine-grained terrigenous sediments starting from 3.5 billion years ago. This finding is consistent with an early onset of plate tectonics. We estimate the geothermal gradient in the Archaean upper continental crust by tracking the reconstructed concentrations of the radiogenic heat-producing elements K, U, and Th through time. Radioactive heat production in the bulk continental crust was 50% higher in the Archaean compared to the present, resulting in a continental geothermal gradient that was about 40% higher
Titanium isotopic compositions of bulk rocks and mineral separates from the Kos magmatic suite: Insights into fractional crystallization and magma mixing processes
Terrestrial and extraterrestrial rocks exhibit significant variations in their mass-dependent Ti isotopic compositions, with basalts being isotopically lighter than evolved lithologies. The observed trend from light to heavy Ti isotopic compositions from more primitive to more differentiated rocks agrees with theoretical predictions that light Ti isotopes are sequestered in Fe–Ti oxides. However, there are lingering questions about the exact extent of this fractionation and whether it is influenced by the nature of oxides and silicate melt. To improve on this matter, we measured the Ti isotopic compositions of mineral separates and bulk rocks from the calc-alkaline Kos volcano-plutonic system, Aegean arc, Greece. Bulk rock Ti isotopic compositions (δ49Ti) increase with differentiation of the magmatic system, from δ49Ti of +0.042 ± 0.033‰ in basalt to +0.654 ± 0.034‰ in rhyolite. We document two different Ti isotope trends produced by (i) fractional crystallization, and (ii) mixing between a basaltic melt and an evolved (rhyolitic) magma. Trend (i) can be explained by a melt-cumulate Ti isotopic fraction factor α of 0.9998 (i.e., the bulk cumulate is on average 0.20‰ lighter than the melt). The mineral separates reveal variable δ49Ti values, with magnetite having the lightest 49Ti/47Ti isotopic composition, biotite being intermediate and neso- and tectosilicates (i.e., olivine, plagioclase and quartz) heaviest. Comparing the TiO2 concentrations of the low-Ti minerals olivine, plagioclase and quartz determined with LA-ICP-MS and isotope dilution shows that the δ49Ti values measured in these minerals reflect their isotopic compositions, and contamination by inclusions is minimal. The difference in δ49Ti between different minerals is smallest in a basalt (Δ49Tiolivine-magnetite = +0.426) and largest in two rhyolites (Δ49Tiquartz-magnetite = +1.083; both ± 0.046‰). Our data agree with theoretical predictions that Fe–Ti oxides have a light δ49Ti signature, and neso/tectosilicate minerals are heavy. Furthermore, the measured difference in δ49Ti between magnetite-olivine, magnetite-plagioclase and magnetite-quartz agree to first order with theoretically predicted inter-mineral Ti isotopic fractionation factors, thus suggesting that the measured inter-mineral Ti isotopic variations are equilibrium in nature
The U/Th production ratio and the age of the Milky Way from meteorites and Galactic halo stars
Some heavy elements (with atomic number A > 69) are produced by the 'rapid' (r)-process of nucleosynthesis, where lighter elements are bombarded with a massive flux of neutrons. Although this is characteristic of supernovae and neutron star mergers, uncertainties in where the r-process occurs persist because stellar models are too crude to allow precise quantification of this phenomenon. As a result, there are many uncertainties and assumptions in the models used to calculate the production ratios of actinides (like uranium-238 and thorium-232). Current estimates of the U/Th production ratio range from ∼0.4 to 0.7. Here I show that the U/Th abundance ratio in meteorites can be used, in conjunction with observations of low-metallicity stars in the halo of the Milky Way, to determine the U/Th production ratio very precisely (0.571 -0.031+0.037). This value can be used in future studies to constrain the possible nuclear mass formulae used in r-process calculations, to help determine the source of Galactic cosmic rays, and to date circumstellar grains. I also estimate the age of the Milky Way (14.5-2.2 +2.8 Gyr) in a way that is independent of the uncertainties associated with fluctuations in the microwave background or models of stellar evolution.link_to_subscribed_fulltex
The isotopic nature of the Earth’s accreting material through time
The Earth formed by accretion of Moon-to Mars-size embryos coming from various heliocentric distances. The isotopic nature of these bodies is unknown. However, taking meteorites as a guide, most models assume that the Earth must have formed from a heterogeneous assortment of embryos with distinct isotopic compositions. High-precision measurements, however, show that the Earth, the Moon and enstatite meteorites have almost indistinguishable isotopic compositions. Models have been proposed that reconcile the Earth-Moon similarity with the inferred heterogeneous nature of Earth-forming material, but these models either require specific geometries for the Moon-forming impact or can explain only one aspect of the Earth-Moon similarity (that is, 17 O). Here I show that elements with distinct affinities for metal can be used to decipher the isotopic nature of the Earth's accreting material through time. I find that the mantle signatures of lithophile O, Ca, Ti and Nd, moderately siderophile Cr, Ni and Mo, and highly siderophile Ru record different stages of the Earth's accretion; yet all those elements point to material that was isotopically most similar to enstatite meteorites. This isotopic similarity indicates that the material accreted by the Earth always comprised a large fraction of enstatite-type impactors (about half were E-type in the first 60 per cent of the accretion and all of the impactors were E-type after that). Accordingly, the giant impactor that formed the Moon probably had an isotopic composition similar to that of the Earth, hence relaxing the constraints on models of lunar formation. Enstatite meteorites and the Earth were formed from the same isotopic reservoir but they diverged in their chemical evolution owing to subsequent fractionation by nebular and planetary processes.link_to_subscribed_fulltex
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2005 Nier Prize for Nicolas Dauphas
The Meteoritics & Planetary Science archives are made available by the Meteoritical Society and the University of Arizona Libraries. Contact [email protected] for further information.Migrated from OJS platform February 202
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