|
Ancient Shelf Anoxia |
1 Department of Earth Sciences, University of Leeds, Leeds LS2 9JT, UK
2 School of Earth Sciences, Birmingham University, Birmingham B15 2TT, UK
The majority of British Jurassic dysaerobic and anaerobic facies (black shales) accumulated in rapidly subsiding basinal areas. Exceptionally, during the earliest stages of transgression, organic-rich facies expanded their distribution into more marginal areas. The biofacies of the black shales display a range of species richness values which, when ranked, record an oxygen gradient that is also reflected by gradients in geochemical and sedimentological data. Truly anaerobic facies (no benthic taxa present) are very rare in the British Jurassic. More common are fissile organic-rich shales with discrete, low-diversity horizons of benthos here defined as lower dysaerobic biofacies. These are interpreted to have formed in a generally anoxic environment punctuated by benthic colonization events in response to ephemeral improvements of oxygen levels. Upper dysaerobic biofacies are characterized by slightly higher diversity faunas scattered throughout poorly fissile strata.
The favoured depositional model for the British Jurassic black shales attributes the high preservational values of organic carbon to accumulation in oxygen-deficient waters trapped beneath a stratified water column in the deepest, basinal areas. We propose an expanding puddle model for transgressive black shales. Deep water conditions are envisaged to become proportionally more extensive during early transgression due to the combined effects of subsidence, a rapid rate of sea-level rise and, unique to this portion of the sea-level curve, sediment starvation.
This article has been cited by other articles:
![]() |
P. Doyle, D. G Poire, L. A. Spalletti, D. Pirrie, P. Brenchley, and S. D. Matheos Relative oxygenation of the Tithonian -- Valanginian Vaca Muerta--Chachao formations of the Mendoza Shelf, Neuquen Basin, Argentina Geological Society, London, Special Publications, 2005; 252: 185 - 206. [Abstract] [PDF] |
||||
![]() |
K. D. Martin A re-evaluation of the relationship between trace fossils and dysoxia Geological Society, London, Special Publications, 2004; 228: 141 - 156. [Abstract] [PDF] |
||||
![]() |
N. R. Ainsworth, W. Braham, F. J. Gregory, B. Johnson, and C. King The lithostratigraphy of the latest Triassic to earliest Cretaceous of the English Channel and its adjacent areas Geological Society, London, Special Publications, 1998; 133: 103 - 164. [Abstract] [PDF] |
||||
![]() |
D. C. Cole and I. C. Harding Use of palynofacies analysis to define Lower Jurassic (Sinemurian to Pliensbachian) genetic stratigraphic sequences in the Wessex Basin, England Geological Society, London, Special Publications, 1998; 133: 165 - 185. [Abstract] [PDF] |
||||
![]() |
A. HALLAM Estimates of the amount and rate of sea-level change across the Rhaetian Hettangian and Pliensbachian Toarcian boundaries (latest Triassic to early Jurassic) Journal of the Geological Society, 1997; 154: 773 - 779. [Abstract] [PDF] |
||||
![]() |
D. J. Bottjer, K. A. Campbell, J. K. Schubert, and M. L. Droser Palaeoecological models, non-uniformitarianism, and tracking the changing ecology of the past Geological Society, London, Special Publications, 1995; 83: 7 - 26. [Abstract] [PDF] |
||||