Dataset Information

Isotope composition and volume of Earth's early oceans.

ABSTRACT: Oxygen and hydrogen isotope compositions of Earth's seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hydrogen's was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope compositions of ancient seawater. Archaean oceans were depleted in deuterium [expressed as ?D relative to Vienna standard mean ocean water (VSMOW)] by at most 25 ± 5‰, but oxygen isotope ratios were comparable to modern oceans. Mass balance of the global hydrogen budget constrains the contribution of continental growth and planetary hydrogen loss to the secular evolution of hydrogen isotope ratios in Earth's oceans. Our calculations predict that the oceans of early Earth were up to 26% more voluminous, and atmospheric CH(4) and CO(2) concentrations determined from limits on hydrogen escape to space are consistent with clement conditions on Archaean Earth.

SUBMITTER: Pope EC

PROVIDER: S-EPMC3311330 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Isotope composition and volume of Earth's early oceans.

Pope Emily C EC Bird Dennis K DK Rosing Minik T MT

Proceedings of the National Academy of Sciences of the United States of America 20120305 12

Oxygen and hydrogen isotope compositions of Earth's seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hydrogen's was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope c ...[more]

PMID: 22392985

Similar Datasets

Project description:Recent analytical advances have provided means to measure potassium (K) isotopes in various terrestrial materials, but little is known about K distribution and stable isotope composition in the lithospheric mantle because of: (a) common low K abundances, (b) potential contamination and alteration, (c) diversity of mantle rocks and minerals hosting K in different tectonic settings. We report K abundances and δ41K values for well-studied whole-rock (WR) mantle xenoliths (spinel and garnet peridotites and pyroxenites) from mobile belts, a craton, a subduction zone, as well as for K-rich phases (mica, amphibole, silicate glass) and xenolith-bearing volcanic materials (67 samples). The xenolith materials show extremely broad ranges of K content (7 μg/g to 6.6 wt.%) and δ41K (-2.77‰ to 0.62‰). They contrast with the narrow δ41K range for host volcanic materials (-0.53‰ to -0.27‰) and literature data on oceanic basalts (melting products of upwelling asthenosphere: -0.43 ± 0.17‰, 2sd). Amphibole-bearing subduction zone peridotites show the highest WR δ41K values (0.40 to 0.62‰) likely inherited from fluids released into the mantle wedge from subducted oceanic crust. All other WR samples yield negative δ41K: -0.06‰ to -2.77‰ for peridotites and -0.17‰ to -0.52‰ for pyroxenites. The δ41K in K-rich mantle phases range from positive values (0.16 to 0.57‰) for phlogopite in strongly metasomatized peridotites to negative values (-0.27 to -0.94‰) for phlogopite, amphibole and glass pockets from other samples, which cannot be explained by equilibrium inter-mineral fractionation inferred from ab initio calculations. We attribute the broad δ41K variations to (a) isotope fractionation during fluid-rock interaction in the mantle, and (b) distinct sources of K-bearing fluids. Kinetic isotope fractionation during fluid percolation and diffusion is inferred for composite xenoliths (phlogopite and pyroxenite veins in peridotites) that have lower δ41K in the hosts than in the veins due to slower migration of 41K than 39K from the veins (former fluid channels) to host mantle. Overall, the K isotope fractionation in the lithospheric mantle appears to be greater than for magmatic fractionation in the crust. The average δ41K of normal off-craton continental lithospheric mantle calculated from the least altered fertile and lightly metasomatized lherzolites is -0.57 ± 0.28‰ (2sd). This value is within error (though a little lower) of estimates for both continental crust and MORB and OIB mantle sources indicating that these major silicate Earth reservoirs have similar bulk δ41K values, apparently due to low or negligible K isotopic fractionation during their formation by magmatic differentiation and melting. By contrast, K isotopes in modern and fossil subduction zones are fractionated via fluid-related equilibrium and kinetic processes.

Project description:The accretion of volatile-rich material from the outer Solar System represents a crucial prerequisite for Earth to develop oceans and become a habitable planet1-4. However, the timing of this accretion remains controversial5-8. It has been proposed that volatile elements were added to Earth by the late accretion of a late veneer consisting of carbonaceous-chondrite-like material after core formation had ceased6,9,10. This view could not be reconciled with the ruthenium (Ru) isotope composition of carbonaceous chondrites5,11, which is distinct from that of the modern mantle12, or of any known meteorite group5. As a possible solution, Earth's pre-late-veneer mantle could already have contained a fraction of Ru that was not fully extracted by core formation13. The presence of such pre-late-veneer Ru can only be established if its isotope composition is distinct from that of the modern mantle. Here we report the first high-precision, mass-independent Ru isotope compositions for Eoarchaean ultramafic rocks from southwest Greenland, which display a relative 100Ru excess of 22 parts per million compared with the modern mantle value. This 100Ru excess indicates that the source of the Eoarchaean rocks already contained a substantial fraction of Ru before the accretion of the late veneer. By 3.7 billion years ago, the mantle beneath southwest Greenland had not yet fully equilibrated with late accreted material. Otherwise, no Ru isotopic difference relative to the modern mantle would be observed. If constraints from other highly siderophile elements besides Ru are also considered14, the composition of the modern mantle can only be reconciled if the late veneer contained substantial amounts of carbonaceous-chondrite-like materials with their characteristic 100Ru deficits. These data therefore relax previous constraints on the late veneer and are consistent with volatile-rich material from the outer Solar System being delivered to Earth during late accretion.

Project description:Mass-independent isotope fractionations driven by differences in volumes and shapes of nuclei (the field shift effect) are known in several elements and are likely to be found in more. All-electron relativistic electronic structure calculations can predict this effect but at present are computationally intensive and limited to modeling small gas phase molecules and clusters. Density functional theory, using the projector augmented wave method (DFT-PAW), has advantages in greater speed and compatibility with a three-dimensional periodic boundary condition while preserving information about the effects of chemistry on electron densities within nuclei. These electron density variations determine the volume component of the field shift effect. In this study, DFT-PAW calculations are calibrated against all-electron, relativistic Dirac-Hartree-Fock, and coupled-cluster with single, double (triple) excitation methods for estimating nuclear volume isotope effects. DFT-PAW calculations accurately reproduce changes in electron densities within nuclei in typical molecules, when PAW datasets constructed with finite nuclei are used. Nuclear volume contributions to vapor-crystal isotope fractionation are calculated for elemental cadmium and mercury, showing good agreement with experiments. The nuclear-volume component of mercury and cadmium isotope fractionations between atomic vapor and montroydite (HgO), cinnabar (HgS), calomel (Hg2Cl2), monteponite (CdO), and the CdS polymorphs hawleyite and greenockite are calculated, indicating preferential incorporation of neutron-rich isotopes in more oxidized, ionically bonded phases. Finally, field shift energies are related to Mössbauer isomer shifts, and equilibrium mass-independent fractionations for several tin-bearing crystals are calculated from (119)Sn spectra. Isomer shift data should simplify calculations of mass-independent isotope fractionations in other elements with Mössbauer isotopes, such as platinum and uranium.

Dataset Information

Isotope composition and volume of Earth's early oceans.

Publications

Isotope composition and volume of Earth's early oceans.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets