Isotopically heavy sulfur in nephelinite from Etinde, Cameroon Volcanic Line: implications for the origin of intraplate magmatism

Baldwin, Sophie L.; Kirstein, Linda A.; Fitton, J. Godfrey; Boyce, Adrian J.; Hutchison, William; Marks, Michael A.W.; Stüeken, Eva E.; Hayward, Chris. 2025 Isotopically heavy sulfur in nephelinite from Etinde, Cameroon Volcanic Line: implications for the origin of intraplate magmatism. Chemical Geology, 682, 122748. 10.1016/j.chemgeo.2025.122748

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Official URL: https://doi.org/10.1016/j.chemgeo.2025.122748

Abstract/Summary

Intraplate magmatism has traditionally been linked to anomalously hot mantle (hotspots) transported upwards from deep-sourced mantle plumes. However, many intraplate magmatic provinces lack convincing evidence for a mantle-plume origin, and the Cameroon Volcanic Line (CVL) located on the West African continental margin is one such province. Despite being active for ca. 65 million years, it lacks the time-progressive volcanic activity that would suggest the presence of a fixed mantle hotspot or plume; instead CVL magmatism has been linked to a shallow, enriched asthenospheric source. Etinde, a relatively young (<1 Ma) volcano located at the centre of the CVL on the continent-ocean boundary, is the most silica-undersaturated and incompatible element-enriched volcano in the region and forms the focus of this study. It is constructed almost entirely of feldspar-free nephelinite lava flows, with compositions ranging from olivine nephelinite to felsic leucite nephelinite. We report new sulfide-, sulfate- and bulk-δ34S data for a suite of Etinde rock samples; the first sulfur-isotope data for the CVL. Strong (∼8 ‰) S-isotope fractionation between sulfide and sulfate (haüyne, nosean) phases suggest equilibration temperatures of ∼600 °C, well below the magma solidus temperature and likely due to sub-solidus exsolution of nanoscale sulfide particles from the sulfate phenocryst phases. The most mafic samples from Etinde have been extensively degassed, containing less than 60 ppm sulfur, and therefore cannot be used to constrain the primary δ34S. Instead, we use the intermediate and felsic volcanic rocks, where sulfur is locked in phenocrysts of haüyne and nosean, respectively. Bulk δ34S of these rocks, which best represents the primary magmatic values, ranges from +3.7 ‰ to +6.3 ‰, a heavier signature than previously reported in alkaline igneous rocks. We propose that the heavy sulfur isotope values, together with the extreme silica undersaturation and incompatible element concentrations, reflect enrichment of the mantle source and fingerprint carbonate metasomatism in the mantle beneath the CVL. The heavy sulfur isotopic signature requires low-temperature fractionation and therefore implies the addition of sulfur through subduction processes. Our study has broad geochemical significance in contributing to a growing understanding of sulfur-isotope compositional variability in geochemically enriched mantle globally.

Item Type:	Publication - Article
Digital Object Identifier (DOI):	10.1016/j.chemgeo.2025.122748
ISSN:	00092541
NORA Subject Terms:	Earth Sciences Chemistry
Date made live:	27 Mar 2025 13:46 +0 (UTC)
URI:	https://nora.nerc.ac.uk/id/eprint/539163

Item Type:

Publication - Article

Digital Object Identifier (DOI):

10.1016/j.chemgeo.2025.122748

ISSN:

00092541

NORA Subject Terms:

Earth Sciences
Chemistry

Date made live:

27 Mar 2025 13:46 +0 (UTC)

URI:

https://nora.nerc.ac.uk/id/eprint/539163