Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-24T06:42:16.307Z Has data issue: false hasContentIssue false

Siderite zonation within the Brent Group: microbial influence or aquifer flow?

Published online by Cambridge University Press:  09 July 2018

M. Wilkinson*
Affiliation:
Department of Geology and Geophysics, West Mains Road, University of Edinburgh, Edinburgh EH9 3JW
R. S. Haszeldine
Affiliation:
Department of Geology and Geophysics, West Mains Road, University of Edinburgh, Edinburgh EH9 3JW
A. E. Fallick
Affiliation:
Isotope Geology Unit, Scottish Universities Research and Reactor Centre, East Kilbride G75 0QU
M. J. Osborne
Affiliation:
Department of Geology and Applied Geology, Glasgow University, Glasgow G12 8QQ, UK
*

Abstract

A three-fold zonation can be imaged within authigenic siderite from sandstones of the Brent Group using back-scatter SEM techniques. We interpret this zonation in terms of the biogeochemical zonation of shallow buried sediment. The innermost siderite crystal zone is very Fe rich (95.0±0.5 mol.% FeCO3), with high Mn levels relative to Ca and Mg. This is interpreted as forming within the Fe reduction zone, with Mn from the closely associated Mn reduction zone. The second siderite crystal zone is frequently represented either by an episode of dissolution, or is impure (80±1 mol.% FeCO3), and this corresponds to the sulphate reduction zone. The outer crystal zone is intermediate in composition, and is equated with the zone of methanogenesis (88±1 mol.% FeCO3). Isotopic values cannot be assigned to individual crystal zones. Bulk δ18O values (−2.7 to −13.0‰ V-PDB) are not consistent with precipitation from seawater at low temperatures, but suggest meteoric pore-waters. δ13C data (−4.3 to −15.7‰ V-PDB) are consistent with microbially-mediated precipitation.

Pyrite and siderite are usually mutually exclusive within a single sample. Sedimentary conditions which favour the development of a strong sulphate reduction zone, and hence the formation of pyrite, do not favour the formation of a strong sub-oxic zone, where siderite is preferentially precipitated, and vice versa. There is a strong facies control upon siderite formation, with ripple cross-laminated sands being most strongly siderite cemented.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Berner, R.A. (1981) A new geochemical classification of sedimentary environments. J. Sed. Res. 51, 51359.Google Scholar
Brint, J.F. (1989) Isotope diagenesis and paleofluid movement: Middle Jurassic Brent Sandstones, North Sea. PhD thesis, Univ. Strathclyde, Scotland.Google Scholar
Canfield, D.E. & Raiswell, R. (1991) Carbonate dissolution and precipitation. Pp. 411-453 in: Taphonomy: Releasing the Data Locked in the Fossil Record (Allison, P.A. & Briggs, D.E.G., editors). Plenum Press, London.Google Scholar
Coleman, M.L. (1985) Geochemistry of diagenetic nonsilicate minerals: kinetic considerations. Pp. 39-54 in: Geochemistry of Buried Sediments (Eglinton, G., editor). Royal Society, London.Google Scholar
Fisher, Q.J., Raiswell, R. & Marshall, J.D. (1998) Siderite concretions from non-marine shales (Westphalian A) of the Pennines, England: controls on their growth and composition. J. Sed. Res. 68, 681034.Google Scholar
Froelich, P.N., Klinkhammer, G.P., Bender, M.L., Luedtke, N.A., Heath, G.R., Cullen, D., Dauphin, P., Hammond, B. & Maynard, V. (1979) Early oxidation of organic matter in pelagic sediments of the eastern equatorial Atlantic. Geochim. Cosmochim. Acta, 43, 431075.Google Scholar
Giles, M.R., Stevenson, S., Martin, S.V., Cannon, S.J.C., Hamilton, P.J., Marshall, J.D. & Samways GM. (1992) The reservoir properties and diagenesis of the Brent Group: a regional perspective. Pp. 289-327 in: Geology of the Brent Group, (Morton, A.C., Haszeldine, R.S., Giles, M.R. & Brown, S., editors). Geological Society London. Spec. Publ. 61.Google Scholar
Haszeldine, R.S., Brint, J.F., Fallick, A.E., Hamilton, P.J. and Brown, S. (1992) Open and restricted hydrologies in Brent Group diagenesis: North Sea. Pp. 401-419 in: Geology of the Brent Group, (Morton, A.C., Haszeldine, R.S., Giles, M.R. & Brown, S., editors). Geological Society London, Spec. Publ. 61.Google Scholar
Hudson, J.D. & Andrews, J.E. (1987) The diagenesis of the Great Estuarine Group, Middle Jurassic, Inner Hebrides, Scotland. Pp. 259-276 in: Diagenesis of Sedimentary Sequences (Marshall, I.D., editor). Geological Society London, Spec. Publ. 36.Google Scholar
Irwin, H., Curtis, C.D. & Coleman, M. (1977) Isotopic evidence for sources of diagenetic carbonates formed during burial of organic-rich sediments. Nature, 269, 269209.Google Scholar
Jeans, C.V., Fallick, A.E., Fisher, M.J., Merriman, R.J., Corfield, R.M. & Manighetti, B. (1997) Clay- and zeolite-bearing Triassic sediments at Kaka Point, New Zealand: evidence of microbially influenced mineral formation from earliest diagenesis into the lowest grade of metamorphism. Clay Miner. 32, 32373.Google Scholar
Macaulay, C.I., Boyce, A.J., Fallick, A.E. & Haszeldine, R.S. (1997) Quartz veins record vertical flow at a graben edge: Fulmar Oil Field, Central North Sea. Am. Soc. Petrol. Geol. Bull. 81, 812024.Google Scholar
Mortimer, R.J.G. & Coleman, M.L. (1997) Microbial influence on the oxygen isotopic composition of diagenetic siderite. Geochim. Cosmochim. Acta, 61, 611705.Google Scholar
Mortimer, R.J.G., Coleman, M.L. & Rae, J.E. (1997) Effect of bacteria on the elemental composition of early diagenetic siderite: implications for palaeoenvironmental interpretations. Sedimentology, 44, 44759.Google Scholar
Morton, A.C., Haszeldine, R.S., Giles, M.R. and Brown, S. (1992) Geology of the Brent Group, Geological Society London, Spec. Publ. 61.Google Scholar
Mozley, P.S. (1989) Relation between depositional environment and the elemental composition of early diagenetic siderite. Geology, 17, 17704.Google Scholar
Mozley, P.S. & Burns, S.J. (1993) Oxygen and carbon isotopic composition of marine carbonate concretions: an overview. J. Sed. Pet. 63, 6373.Google Scholar
Mozley, P.S. & Carothers, W.W. (1992) Elemental and isotopic composition of siderite in the Kuparuk Formation, Alaska - effect of microbial activity and water-sediment interaction on early pore-water chemistry. J. Sed. Pet, 62, 62681.Google Scholar
Mozley, P.S. & Wersin, P. (1992) Isotopic composition of siderite as an indicator of depositional environment. Geology, 20, 20817.Google Scholar
Pye, K., Dickinson, J.A.D., Schiavon, N., Coleman, M.L. & Cox, M. (1990) Formation of siderite-Mg-calciteiron sulphide concretions in intertidal marsh and sandflat sediments, north Norfolk, England. Sedimentology, 37, 37325.Google Scholar
Rude, R.P. & Aller, R.C. (1989) Early diagenetic alteration of lateritic particle coatings in Amazon Continental Shelf sediments. J. Sed. Pet. 59, 59704.Google Scholar
Whiticar, M.J., Faber, E. & Schoell, M. (1986) Biogenic methane formation in marine and freshwater environments: CO2 reduction vs. acetate fermentation–isotopic evidence. Geochim. Cosmochim. Acta, 50, 50693.Google Scholar
Wilkinson, M. (1993) Concretions of the Valtos Sandstone Formation of Skye: geochemical indicators of palaeo-hydrology. J. Geol. Soc. 150, 15057.Google Scholar