The University of Southampton
University of Southampton Institutional Repository

Behaviour of Li isotopes during continental weathering: the Bidar laterite profile, India

Behaviour of Li isotopes during continental weathering: the Bidar laterite profile, India
Behaviour of Li isotopes during continental weathering: the Bidar laterite profile, India
Weathering of large basaltic provinces is a major sink of atmospheric carbon dioxide, and is also an important part of the geochemical cycle of many other elements. This study aims to improve our understanding of basaltic weathering by analysis of trace elements and Li isotopes in a lateritic profile developed upon the Deccan Traps flood basalt. At its base, the profile consists of unaltered basalt that has a Li concentration and ?7Li value of ?5 ppm and +2.5‰, respectively, which is upwards progressively altered to a highly weathered laterite (iron-rich) residuum at the surface. High concentrations of Fe2O3 (85 wt.%) at 11 m depth indicate the presence of a palaeowatertable; the transition metals, the rare earth elements (REEs) and U are also strongly enriched in this horizon, whereas fluid mobile elements, such as Li and Rb, are depleted relative to the precursor basalt, and the bulk ?7Li value is very low (?5.5‰). A high proportion of leachable Li is found in this horizon, and this is enriched in 6Li relative to the bulk. We suggest that leaching extracts the labile weathering products, and these have high 6Li as 7Li has been preferentially mobilised during basalt weathering. Throughout the rest of the profile, Li concentrations and Li isotope values are best explained by two-component mixing between the precursor basalt and aeolian material with high Li and low ?7Li. Mass balance calculations show that at least 50% of the Li present in the profile could have been supplied by a mineral aerosol that has a ?7Li value between 0‰ and +1.3‰. The depth-integrated ?7Li value of the profile is ?0.6‰, which suggests that 7Li has been preferentially leached from the aerosol after its deposition. The source of this aeolian material is most likely to be ancient continental crust. It is possibly derived from Archaen/Proterozoic terrain to the south and southeast of the Deccan, and/or material from central Asia, similar to that which forms Chinese loess and which is supplied to the North Pacific basin.
Lithium isotopes, Weathering, Laterites, Deccan
0009-2541
27-44
Kısakürek, Başak
85dd2f36-496e-451d-83de-2d5476e43909
Widdowson, Mike
9c8f9bd8-738a-42ff-a407-033fc3c5ad50
James, Rachael H.
79aa1d5c-675d-4ba3-85be-fb20798c02f4
Kısakürek, Başak
85dd2f36-496e-451d-83de-2d5476e43909
Widdowson, Mike
9c8f9bd8-738a-42ff-a407-033fc3c5ad50
James, Rachael H.
79aa1d5c-675d-4ba3-85be-fb20798c02f4

Kısakürek, Başak, Widdowson, Mike and James, Rachael H. (2004) Behaviour of Li isotopes during continental weathering: the Bidar laterite profile, India. Chemical Geology, 212 (1-2), 27-44. (doi:10.1016/j.chemgeo.2004.08.027).

Record type: Article

Abstract

Weathering of large basaltic provinces is a major sink of atmospheric carbon dioxide, and is also an important part of the geochemical cycle of many other elements. This study aims to improve our understanding of basaltic weathering by analysis of trace elements and Li isotopes in a lateritic profile developed upon the Deccan Traps flood basalt. At its base, the profile consists of unaltered basalt that has a Li concentration and ?7Li value of ?5 ppm and +2.5‰, respectively, which is upwards progressively altered to a highly weathered laterite (iron-rich) residuum at the surface. High concentrations of Fe2O3 (85 wt.%) at 11 m depth indicate the presence of a palaeowatertable; the transition metals, the rare earth elements (REEs) and U are also strongly enriched in this horizon, whereas fluid mobile elements, such as Li and Rb, are depleted relative to the precursor basalt, and the bulk ?7Li value is very low (?5.5‰). A high proportion of leachable Li is found in this horizon, and this is enriched in 6Li relative to the bulk. We suggest that leaching extracts the labile weathering products, and these have high 6Li as 7Li has been preferentially mobilised during basalt weathering. Throughout the rest of the profile, Li concentrations and Li isotope values are best explained by two-component mixing between the precursor basalt and aeolian material with high Li and low ?7Li. Mass balance calculations show that at least 50% of the Li present in the profile could have been supplied by a mineral aerosol that has a ?7Li value between 0‰ and +1.3‰. The depth-integrated ?7Li value of the profile is ?0.6‰, which suggests that 7Li has been preferentially leached from the aerosol after its deposition. The source of this aeolian material is most likely to be ancient continental crust. It is possibly derived from Archaen/Proterozoic terrain to the south and southeast of the Deccan, and/or material from central Asia, similar to that which forms Chinese loess and which is supplied to the North Pacific basin.

This record has no associated files available for download.

More information

Published date: 2004
Keywords: Lithium isotopes, Weathering, Laterites, Deccan
Organisations: Marine Geoscience

Identifiers

Local EPrints ID: 210109
URI: http://eprints.soton.ac.uk/id/eprint/210109
ISSN: 0009-2541
PURE UUID: 72a49a62-63da-402c-a25d-72f722f97dbe
ORCID for Rachael H. James: ORCID iD orcid.org/0000-0001-7402-2315

Catalogue record

Date deposited: 06 Feb 2012 13:36
Last modified: 15 Mar 2024 03:30

Export record

Altmetrics

Contributors

Author: Başak Kısakürek
Author: Mike Widdowson

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×