9 research outputs found

    Unravelling the controls on the molybdenum isotope ratios of river waters

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    The molybdenum (Mo) isotope ratios (δ98/95Mo) of river waters control the δ98/95Mo values of seawater and impact on the use of Mo isotope ratios as a proxy of past redox conditions. The δ98/95Mo values of river waters vary by more than 2 ‰, yet the relative roles of lithology versus fractionation during weathering remain contested. Here, we combine measurements from river waters (δ98/95Modiss), river bed materials (δ98/95MoBM) and soils from locations with contrasting lithology. The δ98/95Mo values of river bed materials (δ98/95MoBM), set by rock type, vary by ~1 ‰ between rivers in New Zealand, the Mackenzie Basin, and Iceland. However, the difference between dissolved and solid phase Mo isotopes (Δ98/95Modiss-BM) varies from +0.3 ‰ to +1.0 ‰. We estimate Mo removal from solution using the mobile trace element rhenium and find that it correlates with Δ98/95Modiss-BM across the sample set. The adsorption of Mo to Fe-Mn-(oxyhydr)oxides can explain the observed fractionation. Together, the amount of Mo released through dissolution and taken up by (oxyhydr)oxide formation on land may cause changes in the δ98/95Mo values of rivers, driving long term changes in the Mo isotope ratios of seawater

    Unravelling the controls on the molybdenum isotopic composition of rivers

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    Formation and crystallisation of the Lunar Magma Ocean (LMO) was one of the most incisive events during the early evolution of the Moon. Lunar Magma Ocean solidification concluded with the coeval formation of K-, REE- and P-rich components (KREEP) and an ilmenite-bearing cumulate (IBC) layer. Gravitational overturn of the lunar mantle generated eruptions of basaltic rocks with variable Ti contents, of which their δ49Ti variations may now reflect variable mixtures of ambient lunar mantle and the IBC. To better understand the processes generating the spectrum of lunar low-Ti and high-Ti basalts and the role of Ti-rich phases such as ilmenite, we determined the mass dependent Ti isotope composition of four KREEP-rich samples, 12 low-Ti, and eight high-Ti mare basalts by using a 47Ti-49Ti double spike. Our data reveal significant variations in δ49Ti for KREEP-rich samples (+0.117 to +0.296 ‰) and intra-group variations in the mare basalts (-0.030 to +0.055 ‰ for low-Ti and +0.009 to +0.115 ‰ for high-Ti basalts). We modelled the δ49Ti of KREEP using previously published HFSE data as well as the δ49Ti evolution during fractional crystallisation of the LMO. Both approaches yield δ49TiKREEP similar to measured values and are in excellent agreement with previous studies. The involvement of ilmenite in the petrogenesis of the lunar mare basalts is further evaluated by combining our results with element ratios of HFSE, U and Th, revealing that partial melting in an overturned lunar mantle and fractional crystallisation of ilmenite must be the main processes accounting for mass dependent Ti isotope variations in lunar basalts. Based on our results we can also exclude formation of high-Ti basalts by simple assimilation of ilmenite by ascending melts from the depleted lunar mantle. Rather, our data are in accord with melting of these basalts from a hybrid mantle source formed in the aftermath of gravitational lunar mantle overturn, which is in good agreement with previous Fe isotope data

    An Abrupt Aging of Dissolved Organic Carbon in Large Arctic Rivers

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    Permafrost thaw in Arctic watersheds threatens to mobilize hitherto sequestered carbon. We examine the radiocarbon activity (F14C) of dissolved organic carbon (DOC) in the northern Mackenzie River basin. From 2003‐2017, DOC‐F14C signatures (1.00 ± 0.04; n = 39) tracked atmospheric 14CO2, indicating export of “modern” carbon. This trend was interrupted in June 2018 by the widespread release of aged DOC (0.85 ± 0.16, n = 28) measured across three separate catchment areas. Increased nitrate concentrations in June 2018 lead us to attribute this pulse of 14C‐depleted DOC to mobilization of previously frozen soil organic matter. We propose export through lateral perennial thaw zones occurred at the base of the active layer weakened by preceding warm summer and winter seasons. Although we are not yet able to ascertain the broader significance of this “anomalous” mobilization event, it highlights the potential for rapid and large‐scale release of aged carbon from permafrost

    Isotope clues on the origin of Mg/Si variations in chondrites and planetary bodies

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    73rd Annual Meeting of the Meteoritical-Society ; New York, NY ; July 26-30, 2010International audienc

    The magnesium isotope budget of the modern ocean: Constraints from riverine magnesium isotope ratios

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    International audienceWe have measured the magnesium (Mg) isotope ratios in 45 rivers including 16 of the largest rivers in the world, covering a range of geologic, tectonic and climatic drainage basin environments. The range in riverine δ26Mg is 2.5‰, half the variation in terrestrial rock. Although the Mg isotopic composition of the source rock is important for small rivers, at a global scale lithology is of limited significance for Mg isotope ratios in rivers. Part of the variability at a global scale may be attributed to fractionation in the weathering environment. The rivers analysed constitute 30% of the global Mg riverine flux to the oceans and a flux weighted Mg isotope composition of global runoff has been estimated at − 1.09‰. Even taking into account uncertainty, this is distinct from seawater at − 0.82‰. This difference arises either from the fractionation of Mg isotope ratios in the ocean and/or a Mg budget which is not at steady state. The difference is consistent with fractionation by carbonate precipitation. In the simplest steady state scenario, where the oceanic mass balance is maintained by riverine input and hydrothermal and dolomite output, Mg isotope ratios imply a minimum dolomite Mg flux of 9% of the total output Mg flux. The implications of the distinct isotopic composition of the riverine flux from modern seawater, is that the Mg isotope ratio of seawater has probably varied outside of current analytical uncertainty. Mg isotope ratios may therefore provide a valuable new tracer in palaeo-oceanography
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