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Experimental constraints on barium isotope fractionation during adsorption–desorption reactions: Implications for weathering and erosion tracer applications

Authors

Knight,  Alasdair C. G.
External Organizations;

Tipper,  Edward T.
External Organizations;

Bradbury,  Harold J.
External Organizations;

Turchyn,  Alexandra V.
External Organizations;

/persons/resource/alpha01

Andermann,  C.
4.6 Geomorphology, 4.0 Geosystems, Departments, GFZ Publication Database, Deutsches GeoForschungsZentrum;

Freymuth,  Heye
External Organizations;

Elliott,  Tim
External Organizations;

Bridgestock,  Luke
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5028926.pdf
(Publisher version), 4MB

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Citation

Knight, A. C. G., Tipper, E. T., Bradbury, H. J., Turchyn, A. V., Andermann, C., Freymuth, H., Elliott, T., Bridgestock, L. (2024): Experimental constraints on barium isotope fractionation during adsorption–desorption reactions: Implications for weathering and erosion tracer applications. - Geochimica et Cosmochimica Acta, 384, 194-212.
https://doi.org/10.1016/j.gca.2024.08.016


Cite as: https://gfzpublic.gfz-potsdam.de/pubman/item/item_5028926
Abstract
Constraining the processes that fractionate barium isotopes is essential for utilising barium isotope ratios as environmental tracers. Barium concentration measurements from soils, rivers, and estuaries demonstrate that adsorption–desorption reactions significantly influence the distribution of fluid–mobile barium at the Earth’s surface, potentially driving isotopic fractionation. To quantify the direction and magnitude of isotopic fractionation resulting from these reactions, a riverine and an estuarine series of batch experiments were conducted using environmentally important adsorbent minerals and surface waters. Himalayan river sediment and water samples were used to validate the experimental results. Adsorption–desorption reactions were found to be rapid, relative to the average transit time of sediment and water in catchments, and largely reversible. The direction and magnitude of isotopic fractionation in the riverine experiment series were consistent with the riverine field samples (preferential adsorption of the lighter isotopes). The reaction rate, reversibility, and magnitude of isotopic fractionation were found to depend primarily on the mineral. Experiments performed with iron oxyhydroxides (goethite and ferrihydrite) resulted in a greater degree of fractionation compared to clay minerals (kaolinite and montmorillonite). Estuarine experiments, designed to simulate sediment passage through a salinity gradient, demonstrated a high degree of reversibility, with 77% to 94% of adsorbed barium desorbed upon the addition of seawater to freshwater-equilibrated clay minerals. The results of the estuarine experiments suggest that barium isotope ratios measured in marine paleo-archives (e.g., corals) will reflect both the adsorbed and dissolved freshwater barium inputs to the ocean. The combined findings of this study indicate that the chemical and isotopic behaviour of barium differs from more conventional group 1 and 2 metal isotope systems due to a significant proportion of barium released from bedrock dissolution partitioning to mineral surfaces, rapid reaction rates between fluid–mobile phases, and a high degree of reaction reversibility. Consequently, riverine barium isotope ratios are likely to provide unique insights into the complex array of terrestrial weathering and erosion processes that sustain life on Earth.