Genetic studies of red bed mineralization in the Triassic of the Cheshire Basin, northwest England

Naylor, H., Turner, P., Vaughan, D. J., Boyce, A.J. and Fallick, A.E. (1989) Genetic studies of red bed mineralization in the Triassic of the Cheshire Basin, northwest England. Journal of the Geological Society, 146(4), pp. 685-699. (doi: 10.1144/gsjgs.146.4.0685)

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The Triassic sediments of the Cheshire Basin are host to a number of small mineral deposits characteristic of red beds. The mineralization comprises Cu and Pb with minor Zn, Ag, CO, V, Ni, As, Sb and Mn which, together with widespread barite mineralization, is closely associated with basin margin faults. The Wilmslow Sandstone Formation is cemented by authigenic quartz overgrowths enclosing iron sulphides, which predate the main sulphide cements of tennantite, bornite and sulpharsenides. Studies on late calcite-hosted fluid inclusions show homogenization temperatures ranging between 60–70 oC (regarded as the minimum temperature of mineralization) and salinities of 9–22 wt% equivalent NaCl (mean = 17wt%), indicating that the mineralizing fluids were warm and saline. Consideration of the basin history suggests that fluid temperatures in the Permo-Triassic sequence may have reached 150 °C at the time of mineralization. New data significantly constrain the genetic hypothesis for the deposits, refuting a magmatic origin. A basin brine expulsion model is favoured. The sulphur isotope data from the barite mineralization (mean δ34S = +17‰) suggest that the bulk of the barite sulphur was derived directly from the Upper Triassic evaporites (mean δ 34S = +19‰), whilst the distribution of δ 34S values for sulphides (–1.8‰ to +16.2‰) is consistent with ultimate derivation of sulphur from the evaporites by closed system reduction of a sulphate-bearing brine. It seems likely that the reducing agent was organic material (methane) derived from the underlying Coal Measures, but it is uncertain at present whether the principal mechanism was thermochemical or bacterial reduction. The pattern of sulphide δ 34S favours the former process.

Item Type:Articles
Glasgow Author(s) Enlighten ID:Boyce, Professor Adrian and Fallick, Professor Anthony
Authors: Naylor, H., Turner, P., Vaughan, D. J., Boyce, A.J., and Fallick, A.E.
College/School:College of Science and Engineering > Scottish Universities Environmental Research Centre
Journal Name:Journal of the Geological Society
Publisher:Geological Society of London
ISSN (Online):2041-479X

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