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The impact of oxic alteration on plume-derived transition metals in ridge flank sediments from the East Pacific Rise

The impact of oxic alteration on plume-derived transition metals in ridge flank sediments from the East Pacific Rise
The impact of oxic alteration on plume-derived transition metals in ridge flank sediments from the East Pacific Rise
We describe transition metal behaviour during early diagenesis in sediments collected along a transect across the eastern flank of the East Pacific Rise (EPR) at 14°S overlying crust with magnetic ages of 0.36 Ma to 4.6 Ma.

The sediments are lithologically simple and consist of biogenic carbonate, hydrothermal plume precipitates and minor basaltic debris. Sedimentation rates range from 1 cm/ka in the near-axis region (0.36 Ma) to 0.1–0.2 cm/ka across the young ridge flank (by 1.9 Ma, or within 142 km from axis). Redox indicators (porewater Mn(II)aq and solid phase Mo/Mn ratios) indicate fully oxic conditions in near-axis sediments, changing to mildly suboxic conditions across the ridge flank.

Sequential extraction analysis of sediments from the 0.36 Ma site indicates that oxic alteration of Fe oxyhydroxides is dominated by transformation of ferrihydrite to goethite, implying that alteration occurs via dissolution followed by nucleation and precipitation. The extent of alteration (amorphous Fe/total plume-derived Fe) ranges from 0.3 to 0.8, and the time to half conversion is on the order of 100 ka. V associated with plume-derived ferrihydrite is strongly discriminated against during alteration to goethite and the distribution coefficient (DV = (V/Fe)goethite/(V/Fe)dissolved) is in the range 0.45–0.59. Cu, Zn and Ni are delivered to the sediment in association with both Fe oxyhydroxides and Mn oxides, where 70% of Cu and Zn and 10% of Ni are associated with Fe oxyhydroxides. The Fe-adsorbed Cu and Zn are incorporated quantitatively into the lattice structure of goethite during alteration. The Fe-associated Ni most likely represents Ni co-precipitated as Ni–Fe ferrihydrite and incorporated into goethite during alteration. Co is associated only with Mn oxides. The oxic alteration of hydrothermal Fe oxyhydroxides therefore represents a relatively permanent sink (where goethite dissolution is a prerequisite for metal release) for a maximum of 70% of plume-derived Cu and Zn, 50% of V, 10% of Ni and 0% of Co. In oxic sediments, the remaining plume-derived metals are retained in association with amorphous Fe oxyhydroxides and Mn oxides, although this fraction is highly susceptible to diagenetic remobilization under suboxic conditions.
East Pacific Rise, Nazca Plate, hydrothermal sediments, geochemistry, transition metals
0025-3227
133-157
Dunk, R.M.
80f3f571-239d-43b8-8552-0068f7b5e82a
Mills, R.A.
a664f299-1a34-4b63-9988-1e599b756706
Dunk, R.M.
80f3f571-239d-43b8-8552-0068f7b5e82a
Mills, R.A.
a664f299-1a34-4b63-9988-1e599b756706

Dunk, R.M. and Mills, R.A. (2006) The impact of oxic alteration on plume-derived transition metals in ridge flank sediments from the East Pacific Rise. Marine Geology, 229 (3-4), 133-157. (doi:10.1016/j.margeo.2006.03.007).

Record type: Article

Abstract

We describe transition metal behaviour during early diagenesis in sediments collected along a transect across the eastern flank of the East Pacific Rise (EPR) at 14°S overlying crust with magnetic ages of 0.36 Ma to 4.6 Ma.

The sediments are lithologically simple and consist of biogenic carbonate, hydrothermal plume precipitates and minor basaltic debris. Sedimentation rates range from 1 cm/ka in the near-axis region (0.36 Ma) to 0.1–0.2 cm/ka across the young ridge flank (by 1.9 Ma, or within 142 km from axis). Redox indicators (porewater Mn(II)aq and solid phase Mo/Mn ratios) indicate fully oxic conditions in near-axis sediments, changing to mildly suboxic conditions across the ridge flank.

Sequential extraction analysis of sediments from the 0.36 Ma site indicates that oxic alteration of Fe oxyhydroxides is dominated by transformation of ferrihydrite to goethite, implying that alteration occurs via dissolution followed by nucleation and precipitation. The extent of alteration (amorphous Fe/total plume-derived Fe) ranges from 0.3 to 0.8, and the time to half conversion is on the order of 100 ka. V associated with plume-derived ferrihydrite is strongly discriminated against during alteration to goethite and the distribution coefficient (DV = (V/Fe)goethite/(V/Fe)dissolved) is in the range 0.45–0.59. Cu, Zn and Ni are delivered to the sediment in association with both Fe oxyhydroxides and Mn oxides, where 70% of Cu and Zn and 10% of Ni are associated with Fe oxyhydroxides. The Fe-adsorbed Cu and Zn are incorporated quantitatively into the lattice structure of goethite during alteration. The Fe-associated Ni most likely represents Ni co-precipitated as Ni–Fe ferrihydrite and incorporated into goethite during alteration. Co is associated only with Mn oxides. The oxic alteration of hydrothermal Fe oxyhydroxides therefore represents a relatively permanent sink (where goethite dissolution is a prerequisite for metal release) for a maximum of 70% of plume-derived Cu and Zn, 50% of V, 10% of Ni and 0% of Co. In oxic sediments, the remaining plume-derived metals are retained in association with amorphous Fe oxyhydroxides and Mn oxides, although this fraction is highly susceptible to diagenetic remobilization under suboxic conditions.

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More information

Published date: 2006
Keywords: East Pacific Rise, Nazca Plate, hydrothermal sediments, geochemistry, transition metals

Identifiers

Local EPrints ID: 41210
URI: http://eprints.soton.ac.uk/id/eprint/41210
ISSN: 0025-3227
PURE UUID: 812fab14-1c55-49dd-8c35-8d2125ccd44b
ORCID for R.A. Mills: ORCID iD orcid.org/0000-0002-9811-246X

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Date deposited: 28 Jul 2006
Last modified: 16 Mar 2024 02:45

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Contributors

Author: R.M. Dunk
Author: R.A. Mills ORCID iD

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