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Marine geochemical cycles of the alkali elements and boron: the role of sediments

Marine geochemical cycles of the alkali elements and boron: the role of sediments
Marine geochemical cycles of the alkali elements and boron: the role of sediments
We have analysed the concentrations of Li, K, Rb, Cs, and B, and the isotopic ratios of Li and B of a suite of pore fluids recovered from ODP Sites 1037 (Leg 169; Escanaba Trough) and 1034 (Leg 169S; Saanich Inlet). In addition, we have analysed dissolved K, Rb, and Cs concentrations for estuarine mixing of the Ganges–Brahmaputra river system. Together, these data sets have been used to assess the role of sediments in the marine geochemical cycles of the alkali elements and boron.

Uptake onto clay minerals during estuarine mixing removes 20–30% of the riverine input of dissolved Cs and Rb to the oceans. Prior to this study, the only other recognised sink of Rb and Cs was uptake during low-temperature alteration of the oceanic crust. Even with this additional sink there is an excess of inputs over outputs in their modern oceanic mass balance. Pore fluid data show that Li and Rb are transferred into marine sediments during early diagenesis. However, modeling of the Li isotope systematics of the pore fluids from Site 1037 shows that seawater Li taken up during marine sedimentation can be readily returned to solution in the presence of less hydrated cations, such as NH4+. This process also appears to result in high concentrations of pore fluid Cs (relative to local seawater) due to expulsion of adsorbed Cs from cation exchange sites.

Flux calculations based on pore fluid data for a series of ODP sites indicate that early diagenesis of clay sediments removes around 8% of the modern riverine input of dissolved Li. Although NH4+-rich fluids do result in a flux of Cs to the oceans, on the global scale this input only augments the modern riverine Cs flux by ~3%. Nevertheless, this may have implications for the fate of radioactive Cs in the natural environment and waste repositories.
0016-7037
3111-3122
James, R.H.
79aa1d5c-675d-4ba3-85be-fb20798c02f4
Palmer, M.R.
d2e60e81-5d6e-4ddb-a243-602537286080
James, R.H.
79aa1d5c-675d-4ba3-85be-fb20798c02f4
Palmer, M.R.
d2e60e81-5d6e-4ddb-a243-602537286080

James, R.H. and Palmer, M.R. (2000) Marine geochemical cycles of the alkali elements and boron: the role of sediments. Geochimica et Cosmochimica Acta, 64 (18), 3111-3122. (doi:10.1016/S0016-7037(00)00418-X).

Record type: Article

Abstract

We have analysed the concentrations of Li, K, Rb, Cs, and B, and the isotopic ratios of Li and B of a suite of pore fluids recovered from ODP Sites 1037 (Leg 169; Escanaba Trough) and 1034 (Leg 169S; Saanich Inlet). In addition, we have analysed dissolved K, Rb, and Cs concentrations for estuarine mixing of the Ganges–Brahmaputra river system. Together, these data sets have been used to assess the role of sediments in the marine geochemical cycles of the alkali elements and boron.

Uptake onto clay minerals during estuarine mixing removes 20–30% of the riverine input of dissolved Cs and Rb to the oceans. Prior to this study, the only other recognised sink of Rb and Cs was uptake during low-temperature alteration of the oceanic crust. Even with this additional sink there is an excess of inputs over outputs in their modern oceanic mass balance. Pore fluid data show that Li and Rb are transferred into marine sediments during early diagenesis. However, modeling of the Li isotope systematics of the pore fluids from Site 1037 shows that seawater Li taken up during marine sedimentation can be readily returned to solution in the presence of less hydrated cations, such as NH4+. This process also appears to result in high concentrations of pore fluid Cs (relative to local seawater) due to expulsion of adsorbed Cs from cation exchange sites.

Flux calculations based on pore fluid data for a series of ODP sites indicate that early diagenesis of clay sediments removes around 8% of the modern riverine input of dissolved Li. Although NH4+-rich fluids do result in a flux of Cs to the oceans, on the global scale this input only augments the modern riverine Cs flux by ~3%. Nevertheless, this may have implications for the fate of radioactive Cs in the natural environment and waste repositories.

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More information

Published date: 2000
Organisations: Marine Geoscience

Identifiers

Local EPrints ID: 1342
URI: http://eprints.soton.ac.uk/id/eprint/1342
ISSN: 0016-7037
PURE UUID: b8f169b4-fb2c-4af5-81e5-73a50bb8aad6
ORCID for R.H. James: ORCID iD orcid.org/0000-0001-7402-2315

Catalogue record

Date deposited: 16 Apr 2004
Last modified: 16 Mar 2024 03:57

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