Constraining the drivers of barium isotope composition in marine barite: Insights from Pliocene-Holocene Eastern Mediterranean sapropels

The stable isotopic composition of barium in marine barite ( δ 138/134 Ba barite ) has been proposed as a proxy for reconstructing past Ba cycling in the oceanic water column. However, whether δ 138/134 Ba barite can also be a proxy for export productivity remains uncertain, particularly in semi-enclosed basins such as the Eastern Mediterranean (EMed). Here we present the first record of δ 138/134 Ba barite extracted from EMed Pliocene to Holocene sapropels from six Ocean Drilling Program (ODP) Sites. Despite strong variability in Ba concentrations (∼400–4000 ppm) and organic carbon content (∼3–25 %)—reflecting varying export productivity levels—the δ 138/134 Ba barite values show limited variation (ranging between 0.02 to −0.16 ‰), even during periods of exceptionally high inferred export productivity (e.g., during late Pleistocene sapropel S5). Consistent δ 138/134 Ba barite values are also observed in sapropel S1 sites located at a wide range of water depths (∼900–3600 m). Well-preserved pelagic barite crystal textures (observed under scanning electron microscopy) and barite sulphur isotope composition similar to seawater (∼21 ‰; Paytan et al., 2004) in the sapropels, suggest that neither partial dissolution in bottom waters nor postdeposition Ba ion-exchange significantly altered the δ 138/134 Ba barite signal. These results suggest that fluctuations in marine productivity had a limited impact on the dissolved Ba pool and its isotopic composition in the EMed upper water column during sapropel deposition. Instead, the EMed δ 138/134 Ba was likely controlled primarily by the Ba isotope composition of Atlantic Water inflow and local dissolved Ba sources, such as riverine and groundwater inputs, rather than by productivity-driven barite fluxes. This finding highlights that δ 138/134 Ba barite in sedimentary records should not be interpreted as a straightforward proxy for export productivity, particularly in semi-restricted basins.

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Journal
Geochimica et Cosmochimica Acta
Published
2025-11-25
DOI
https://doi.org/10.1016/j.gca.2025.11.042
Primary Topic
Calcium Carbonate Crystallization and Inhibition
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article
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article

Constraining the drivers of barium isotope composition in marine barite: Insights from Pliocene-Holocene Eastern Mediterranean sapropels

Ricardo Monedero-Contreras, Ed C. Hathorne, Francisca Martínez‐Ruiz, Martin Frank et al.
Geochimica et Cosmochimica Acta
Calcium Carbonate Crystallization and Inhibition
article

Constraining the drivers of barium isotope composition in marine barite: Insights from Pliocene-Holocene Eastern Mediterranean sapropels

Ricardo Monedero-Contreras, Ed C. Hathorne, Francisca Martínez‐Ruiz, Martin Frank, Adina Paytan
article en

Abstract

The stable isotopic composition of barium in marine barite ( δ 138/134 Ba barite ) has been proposed as a proxy for reconstructing past Ba cycling in the oceanic water column. However, whether δ 138/134 Ba barite can also be a proxy for export productivity remains uncertain, particularly in semi-enclosed basins such as the Eastern Mediterranean (EMed). Here we present the first record of δ 138/134 Ba barite extracted from EMed Pliocene to Holocene sapropels from six Ocean Drilling Program (ODP) Sites. Despite strong variability in Ba concentrations (∼400–4000 ppm) and organic carbon content (∼3–25 %)—reflecting varying export productivity levels—the δ 138/134 Ba barite values show limited variation (ranging between 0.02 to −0.16 ‰), even during periods of exceptionally high inferred export productivity (e.g., during late Pleistocene sapropel S5). Consistent δ 138/134 Ba barite values are also observed in sapropel S1 sites located at a wide range of water depths (∼900–3600 m). Well-preserved pelagic barite crystal textures (observed under scanning electron microscopy) and barite sulphur isotope composition similar to seawater (∼21 ‰; Paytan et al., 2004) in the sapropels, suggest that neither partial dissolution in bottom waters nor postdeposition Ba ion-exchange significantly altered the δ 138/134 Ba barite signal. These results suggest that fluctuations in marine productivity had a limited impact on the dissolved Ba pool and its isotopic composition in the EMed upper water column during sapropel deposition. Instead, the EMed δ 138/134 Ba was likely controlled primarily by the Ba isotope composition of Atlantic Water inflow and local dissolved Ba sources, such as riverine and groundwater inputs, rather than by productivity-driven barite fluxes. This finding highlights that δ 138/134 Ba barite in sedimentary records should not be interpreted as a straightforward proxy for export productivity, particularly in semi-restricted basins.

Geochimica et Cosmochimica ActaVol. 412
University of California, Santa Cruz (US), GEOMAR Helmholtz Centre for Ocean Research Kiel (DE), Instituto Andaluz de Ciencias de la Tierra (ES)
Openalex Percentile: Top 75%
Calcium Carbonate Crystallization and Inhibition
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