4.7 Article

Redox-sensitive element uptake in north-east Atlantic Ocean sediments (Benthic Boundary Layer Experiment sites)

Journal

EARTH AND PLANETARY SCIENCE LETTERS
Volume 184, Issue 2, Pages 535-547

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0012-821X(00)00347-2

Keywords

deep-sea sedimentation; selenium; uranium; cadmium; rhenium

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Regularly increasing radiocarbon age-depth profiles and near-constant sediment composition with depth have demonstrated that sediment accumulation has been relatively constant during the late Holocene at two north-east Atlantic sites on Rockall Bank and Feni Drift (UK Benthic Boundary Layer Experiment sites). In such a quasi-steady state situation, the geochemical responses to early diagenesis of the redox-sensitive elements Cd, Mn, Mo, Re, Se and U are readily discerned through changes in element concentrations with depth. Collectively, a colour change in the sediments, surficial MnOx-enriched layers and Pb-210(excess) profiles allow an estimate of the mean position of the oxic-post-oxic boundary in the sediments at both sites. This boundary is situated deeper than the Pb-210(excess) surface mixed layer but shallower than the C-14 surface mixed layer which represent mixing on 10(2) and 10(3) year time scales, respectively. This implies that the well-defined surface MnOx enrichment and its associated Ra-226 and Mo fractions must have been efficiently recycled first by downwards mixing into anoxic conditions, and then by subsequent reduction and diffusive migration back up into oxic conditions. This occurs in < 40 years at the Feni Drift site and in < 10(3) years at the Rockall Bank site. Authigenic enrichments of Se, Cd and U are evident immediately below the oxic-post-oxic boundary, although Re enrichment does not occur until a few centimetres deeper. The long-term fluxes of authigenic Se, Cd, U and Re uptake are evaluated with steady-state assumptions. While diffusion from bottom waters can supply sufficient Se, U and Re, an additional source (likely C-org) is required for Cd. (C) 2001 Elsevier Science B.V. All rights reserved.

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