Barium cycling in the Gulf of Aqaba

The isotopic composition of barium (δ 138 Ba) has emerged as a powerful tracer of deep-ocean circulation, water mass provenance, and the oceanic Ba cycle. Although the δ 138 Ba of water masses is primarily controlled by the balance between pelagic barite precipitation and Ba resupply from ocean circulation, questions remain regarding the isotopic offset associated with pelagic barite formation and how the resultant Ba isotope compositions are transmitted through the water column to marine sediments. To address these questions, we conducted a time series study of dissolved, particulate, and sedimentary Ba chemistry in the Gulf of Aqaba (GOA), in the northern Red Sea, from January 2015 to April 2016. These data span significant seasonal changes in hydrography, primary productivity, and aerosol deposition, revealing three principal findings. First, the dissolved Ba chemistry of the GOA is vertically uniform across the time series, largely reflecting water mass advection from the Red Sea, with mean dissolved Ba concentrations of 47.9 ± 4.7 nmol kg −1 and mean δ 138 Ba = +0.55‰ ± 0.07‰ (±2 SD, n = 18). Second, despite significant variations in particulate matter composition and flux, the δ 138 Ba of sinking particulate Ba maintained a consistent isotope composition across different depths and over time at +0.09‰ ± 0.06‰ ( n = 26). Consequently, these data imply a consistent Ba isotope offset of −0.46‰ ± 0.10‰ (±2 SD) between sinking particulates and seawater. This offset is similar to those determined in previous studies and indicates that it applies to particulates formed across diverse environmental conditions. Third, barite-containing sediment samples deposited in the GOA exhibit δ 138 Ba = +0.34‰ ± 0.03‰, which is offset by approximately +0.2‰ relative to sinking particles. While the specific mechanism driving this offset remains unresolved, our results highlight the importance of performing site-specific proxy validations and exercising careful site selection when applying novel paleoceanographic proxies.

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Publication Details

Journal
Frontiers in Earth Science
Published
2024-09-12
DOI
https://doi.org/10.3389/feart.2024.1178487
Primary Topic
Groundwater and Isotope Geochemistry
Type
article
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article

Barium cycling in the Gulf of Aqaba

Maureen Auro, Tristan J. Horner, Adi Torfstein, Peter W. Crockford et al.
Frontiers in Earth Science
Groundwater and Isotope Geochemistry
article

Barium cycling in the Gulf of Aqaba

Maureen Auro, Tristan J. Horner, Adi Torfstein, Peter W. Crockford, Adina Paytan, Kimberley K. Mayfield
article en

Abstract

The isotopic composition of barium (δ 138 Ba) has emerged as a powerful tracer of deep-ocean circulation, water mass provenance, and the oceanic Ba cycle. Although the δ 138 Ba of water masses is primarily controlled by the balance between pelagic barite precipitation and Ba resupply from ocean circulation, questions remain regarding the isotopic offset associated with pelagic barite formation and how the resultant Ba isotope compositions are transmitted through the water column to marine sediments. To address these questions, we conducted a time series study of dissolved, particulate, and sedimentary Ba chemistry in the Gulf of Aqaba (GOA), in the northern Red Sea, from January 2015 to April 2016. These data span significant seasonal changes in hydrography, primary productivity, and aerosol deposition, revealing three principal findings. First, the dissolved Ba chemistry of the GOA is vertically uniform across the time series, largely reflecting water mass advection from the Red Sea, with mean dissolved Ba concentrations of 47.9 ± 4.7 nmol kg −1 and mean δ 138 Ba = +0.55‰ ± 0.07‰ (±2 SD, n = 18). Second, despite significant variations in particulate matter composition and flux, the δ 138 Ba of sinking particulate Ba maintained a consistent isotope composition across different depths and over time at +0.09‰ ± 0.06‰ ( n = 26). Consequently, these data imply a consistent Ba isotope offset of −0.46‰ ± 0.10‰ (±2 SD) between sinking particulates and seawater. This offset is similar to those determined in previous studies and indicates that it applies to particulates formed across diverse environmental conditions. Third, barite-containing sediment samples deposited in the GOA exhibit δ 138 Ba = +0.34‰ ± 0.03‰, which is offset by approximately +0.2‰ relative to sinking particles. While the specific mechanism driving this offset remains unresolved, our results highlight the importance of performing site-specific proxy validations and exercising careful site selection when applying novel paleoceanographic proxies.

Frontiers in Earth ScienceVol. 12
Lawrence Livermore National Laboratory (US), University of California, Santa Cruz (US), Hebrew University of Jerusalem (IL), Interuniversity Institute for Marine Sciences in Eilat (IL), Woods Hole Oceanographic Institution (US), Carleton University (CA)
Openalex Percentile: Top 86%
Groundwater and Isotope Geochemistry
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