ALBERT

Description: The Permo-Triassic red bed sequence penetrated in BNOC Well 72/10-1A, located in the Western Approaches, is divided into eight clay mineral zones. The zones are defined by variations in the clay assemblage in which iron- and magnesium-rich chlorite, corrensite and mica occur. This zonal sequence is matched mineralogically and stratigraphically with the pattern of clay mineral variation recorded from the Permo-Triassic sediments of the south Devon coast, some 500 km distant.

Description: The distribution, mineralogy, petrology and bulk and stable isotope chemistry of altered volcanic ash beds in the marine sediments of Mid-Triassic age (Etalian) at Kaka Point, New Zealand, are described and related to lithofacies and the geological processes controlling their development.Three varieties of altered ash occur in the Kaka Point sediments — porcellanite, claystone (bentonite) and albite-rich. Porcellanites are quartz-rich and may contain analcime and heulandite: they are restricted mainly to the on-shore facies. Claystones are rich in smectitic clay minerals and occur in both the on-shore and off-shore facies. They often contain diagenetic nodules of analcime, quartz, apatite and carbonates. The authigenic carbonates of the on-shore facies are variable in composition (sideritic, rhodochrositic, calcitic), whereas in the off-shore facies they consist only of calcite. The albite-rich lithology is very rare and is known only from the off-shore facies.The development of the porcellanite and albite-rich lithologies was restricted to slowly deposited, relatively coarse-grained ash sediments in which extensive interchange took place between the sediment's pore-waters and ambient seawater, resulting in enhanced microbial activity and high pH throughout the pore-waters of the suboxic zone beneath the water-sediment interface. The high pH increased the rate of volcanic ash hydrolysis and provided the conditions necessary for the precipitation of zeolite, feldspar and quartz. The development of smectitic claystones was associated with more rapid deposition and limited interchange between the pore-waters of the parent ash and ambient seawater. The pore-water alkalinity was generally lower and enhanced microbial activity and high pHs were restricted to patches of sediment at which quartz, analcime, apatite and carbonates formed diagenetic nodules. Modelling of the stable isotopes of the smectitic clays (δ18O, δD) and diagenetic carbonates (δ18O, δ13C) suggest that: (1) ash argillization in the on-shore facies took place in brackish water (∼25% meteoric water) at an average temperature of ∼50°C and in the off-shore facies in marine pore-waters (∼10% meteoric waters) at ∼40°C and (2) diagenetic carbonate precipitation in the near-shore facies took place at ∼30°C and in the off-shore facies at 60–80°C.The pattern of ash alteration in the marine Triassic sediments at Kaka Point is considered to represent an early stage in the development of the zeolite pattern associated with the classic area of zeolite facies metamorphism in the Taringatura and Hokonui Hills.

Description: The K/Ar characteristics of 53 clay assemblages (Triassic–Cretaceous), representing the detrital, volcanogenic and arid-facies clay mineral associations, are interpreted in relation to their mineralogy, chronostratic age and geological origins. The K-bearing mineral components of the 1–2 μm, 0.2–1 μm and

Description: The nature and origin of authigenic clay minerals and silicate cements in the Jurassic and Cretaceous sediments of England and the North Sea are discussed in relation to penecontemporaneous volcanism in and around the North Sea Basin. Evidence, including new REE data, suggests that the authigenic clay minerals represent the argillization of volcanic ash under varying diagenetic conditions, and that volcanic ash is a likely source for at least the early silicate cements in many sandstones. The nature and origin of smectite-rich, glauconite-rich, berthierine-rich and kaolin-rich volcanogenic clay mineral deposits are discussed. Two patterns of volcanogenic clay minerals facies are described. Pattern A is related to ash argillization in the non-marine and marine environments. Pattern B is developed by the argillization of ash concentrated in the sand and silt facies belts in the seas bordering ash-covered islands and massifs. It is associated with regression/ transgression cycles which may be related to thermal doming and associated volcanism, including the submarine release of hydrothermal fluids rich in Fe. The apparent paucity of volcanogenic clay deposits in the Jurasssic and Early Cretaceous sediments of the North Sea is discussed.

Description: The origin of the regional and stratigraphical variation in the Triassic authigenic clay assemblages of England is discussed in relation to new estimates of the palaeotemperatures experienced by their host sediments and a preliminary study by transmission electron microscopy of their microtextural features. Spore colour index measurements, based on the spore type Deltoidospora s.l. occurring in the sediments (Penarth Group) at the very top of the Triassic sequence, give estimated palaeotemperatures ranging from 60–74°C (south Devon) to 89–97°C (northeast Yorkshire). Calculated palaeotemperatures, based on a gradient of 25°C/km, for the main zone of authigenic clay minerals range from 63–77°C to 89–97°C for the top to 71–85°C to 94–104°C for the base. Irregular mixed-layer smectite-chlorite, corrensite and Mg-rich chlorite are associated with calculated palaeotemperatures of 66–86°C, 66–104°C and 75–104°C respectively. The suggestion that elsewhere in the UK corrensite and Mg-rich chlorite were formed at temperatures in excess of 100°C finds no support. Geothermal gradients would have to have been of the order of at least 100–300°C/km to obtain these temperatures within the Triassic sediments; such values are associated typically with high-level magmatic intrusions or geothermal systems of which there is no geological evidence. The balance of evidence suggests that the Triassic authigenic clay assemblages formed by neoformation during the early stages of sediment diagenesis under the influence of variation in the alkalinity of the depositional environments.

Description: Clay mica is the predominant component of the fine-grained siliciclastic sediments of the Western European Permo-Trias and it may occur as the sole component of the clay assemblage. Its characteristics have been studied by chemical analysis, radioisotope (K/Ar) data, X-ray diffraction and electron microscopy in the clay assemblages from Triassic and Permian sediments in Spain, Western Approaches, South Devon and East Yorkshire. The clay mica is a ferric dioctahedral mineral containing on average 6.5% Fe2O3 and 7.5% K2O. Crystal thickness ranges from 8 × 10 Å to 115 × 10 Å, and varies with geological, stratigraphical and grain-size factors. Radioisotope data and geological considerations suggest that much of the Permo-Triassic clay mica was formed originally in coeval desert soils rather than being derived from pre-existing rocks. It was then eroded, sometimes mixed with much older material, and deposited as fine-grained detritus in adjacent areas. Upon deep burial, this detrital mica assemblage underwent recrystallization with the development of euhedral crystals and the alteration of the K/Ar values.

Description: A tightly cemented series of marine sandstones, interbedded with shales and mudstones, occurs in the lower part of the Kimmeridge Clay Formation (Kimmeridgian to Ryazanian) of Arco Well 14/26-1 (Core No. 5, 8067–8085 ft). The well is on the northern flank of the Fraserburgh Spur Basement Ridge. The sediments are in the immature stage of hydrocarbon generation and are now at their maximum temperature and burial depth: the bottom hole temperature is 75°C. The sandstone diagenesis was complex, essentially of an intrinsic type, and took place under considerable overpressures. Initially a series of early cements was precipitated (minor chalcedony, quartz, feldspar, ferroan calcite, non-ferroan dolomite and major ferroan dolomite). A later phase of diagenesis embraced two periods of intrastratal solution (each affecting both the silicate and the carbonate components of the sediment) separated by a phase of calcite precipitation and followed by a phase of kaolinite cementation. The early cements are interpreted as being of the intrinsic miagenetic type. The later phase of diagenesis (alternating intrastratal solution and cement precipitation) resulted from the interaction of (i) the biotic breakdown of organic matter by thermophyllic micro-organisms and (ii) the abiotic thermal alteration of organic matter with the mineral components of the sediment: of particular importance were varying PCO2 and the generation of carboxylic and phenolic acids. The diagenetic pattern is closely comparable to that known from various Upper Jurassic sandy shelf sediments in other parts of the northern North Sea which have very different burial histories.