Clay mineralogy of the Permo-Triassic strata of the British Isles: onshore and offshore

Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 309-354 ◽  
Author(s):  
C. V. Jeans

AbstractThe regional distribution, mineralogy, petrology and chemistry of the detrital and authigenic clay minerals associated with the Permo-Triassic strata (excluding the Rotliegend: see Ziegler, 2006; this volume), of the onshore and offshore regions of the British Isles are reviewed within their stratigraphical framework. The origin of these clay minerals is discussed in relation to current hypotheses on the developments of the Mg-rich clay mineral assemblages associated with the evaporitic red-bed Germanic facies of Europe and North Africa.Composite clay mineral successions are described for seven regions of the British Isles — the Western Approaches Trough; SW England; South Midlands; Central Midlands; the Cheshire Basin; NE Yorkshire; and the Central North Sea. The detrital clay mineral assemblages of the Early Permian strata are variable, consisting of mica, smectite, smectite-mica, kaolin and chlorite, whereas those of the Late Permian and the Trias are dominated by mica, usually in association with minor Fe-rich chlorite. The detrital mica consists of a mixture of penecontemporaneous ferric mica, probably of pedogenic origin, and recycled Pre-Permian mica. In the youngest Triassic strata (Rhaetian), the detrital clay assemblages may contain appreciable amounts of poorly defined collapsible minerals (irregular mixed-layer smectite-mica-vermiculite) and kaolin, giving them a Jurassic aspect. There are two types of authigenic clay mineral assemblages. Kaolin may occur as a late-stage diagenetic mineral where the original Permo-Triassic porewaters of the sediment have been replaced by meteoritic waters. A suite of early-stage diagenetic clay minerals, many of them Mg-rich, are linked to the evaporitic red-bed facies — these include sepiolite, palygorskite, smectite, irregular mixed- layer smectite-mica and smectite-chlorite, corrensite, chlorite and glauconite (sensu lato). The sandstones and mudstones of the onshore regions of the British Isles display little or no difference in their detrital and authigenic clay mineral assemblages. In contrast, the sandstones of the offshore regions (North Sea) show major differences with the presence of extensive chloritic cements containing Mg-rich and Al-rich chlorite, irregular mixed-layer serpentine-chlorite, and mica.

Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 187-307 ◽  
Author(s):  
C. V. Jeans

AbstractThe nature and origin of the clay mineralogy of the Jurassic strata of the British Isles are described and discussed within their lithological and biostratigraphical framework using published and unpublished sources as well as 1800 new clay mineral analyses. Regional clay mineral variation is described systematically for the following formations or groups:England and Wales(i)Hettangian-Toarcian strata (Lias Group): Redcar Mudstone Fm.; Staithes Sandstone Fm.; Cleveland Ironstone Fm.; Whitby Mudstone Fm.; Scunthorpe Mudstone Fm.; Blue Lias Fm.; Charmouth Mudstone Fm.; Marlstone Rock Fm.; Dyrham Fm.; Beacon Limestone Fm.; Bridport Sand Fm.(ii)Aalenian-Bajocian (Inferior Oolite Group): Dogger Fm.; Saltwick Fm.; Eller Beck Fm.; Cloughton Fm.; Scarborough Fm.; Scalby Fm. (in part); Northampton Sand Fm.; Grantham Fm.; Lincolnshire Limestone Fm.; Rutland Fm. (in part); Inferior Oolite of southern England.(iii)Bathonian (Great Oolite Group): Scalby Fm. (in part); Rutland Fm. (in part); Blisworth Limestone Fm.; Great Oolite Group of southern England; Forest Marble Fm.; Cornbrash Fm. (in part).(iv)Callovian-Oxfordian: Cornbrash Fm. (in part); Kellaways Fm.; Oxford Clay Fm.; Corallian Beds and West Walton Beds; Ampthill Clay Fm.(v)Kimmeridgian-Tithonian: Kimmeridge Clay Fm.; Portland Sandstone Fm.; Portland Limestone Fm.; Lulworth Fm.; Spilsby Sandstone Fm. (in part). Scotland(vi)Hettangian-Toarcian: Broadfoot Beds, Dunrobin Bay Fm. Aalenian-Portlandian: Great Estuarine Group (Dunkulm, Kilmaluag and Studiburgh Fm.s); Staffin Shale Fm.; Brora Coal Fm.; Brora Argillaceous Fm.; Balintore Fm.; Helmsdale Boulder Beds (Kimmeridge Clay Fm.).Dominating the Jurassic successions are the great marine mudstone formations — the Lias Group, Oxford Clay, Ampthill Clay and Kimmeridge Clay. These are typically characterized by a detrital clay mineral assemblage of mica, kaolin and poorly defined mixed-layer smectite-mica-vermiculite minerals with traces of chlorite. Detailed evidence suggests that this assemblage is derived ultimately from weathered Palaeozoic sediments and metasediments either directly or by being recycled from earlier Mesozoic sediments. A potassium-bearing clay is a persistent component and formed at approximately the same time as the deposition of the host sediment, either in coeval soils or during very early diagenesis.At three periods during the deposition of the Jurassic (Bajocian-Bathonian, Oxfordian and late Kimmeridgian-Tithonian), the detrital clay assemblage was completely or partially replaced by authigenic clay mineral assemblages rich in kaolin, berthierine, glauconite or smectite minerals. Associated with these changes are major changes in the lithofacies, with the incoming of non-marine and proximal marine strata. The authigenic clay assemblages rich in kaolin and berthierine are generally restricted to the non-marine and very proximal marine beds, those rich in glauconite or smectite are typical of the marine lithofacies. Clay mineral assemblages containing vermiculite and mixed-layer vermiculite-chlorite sometimes occur in the non-marine and proximal marine facies. The causes of these major changes in lithofacies and clay mineralogy are discussed, and present evidence favours an important volcanogenic influence and not climatic control. It is suggested that the Bajocian-Bathonian, Oxfordian and Late Kimmeridgian-Tithonian were periods of enhanced volcanic activity, with centres probably located in the North Sea and linked to regional tectonic changes which caused major modifications of the palaeogeography of the British Isles. The most important of these changes was the development of the central North Sea Rift Dome during the Bajocian and Bathonian. Volcanic ash was widespread in both the non-marine and marine environments and its argillization under different conditions provided the wide range of authigenic clay mineral assemblages.Metre-scale clay mineral cyclicity is widespread in most of the Jurassic mudstone formations that have been examined in sufficient detail. The cyclicity is defined by systematic variations in the mica/ collapsible minerals (mixed-layer smectite-mica-vermiculite) ratio. This variation is unrelated to changes in lithology and its possible origins are discussed in detail using data from the Kimmeridge Clay provided by Reading University's contribution to the Rapid Global Geological Events (RGGE) Project.


1987 ◽  
Vol 124 (3) ◽  
pp. 261-271 ◽  
Author(s):  
Julian E. Andrews

AbstractClay minerals from Middle Jurassic lagoonal mudrocks, siltstones and silty fine-grained sandstones of the upper Great Estuarine Group (Bathonian) are divided into four assemblages. Assemblage 1, the most common assemblage, is rich in mixed-layer illite–smectite with attendant illite and kaolinite. Assemblage 2 is dominated by smectitic clay. These assemblages are indicative of primary Jurassic deposition. Illite and kaolinite were probably derived from the weathering of older rocks and soils in the basin hinterland and were deposited in the lagoons as river-borne detritus. The majority of smectite and mixed-layer illite–smectite is interpreted as the argillization product of Jurassic volcanic dust, also deposited in the lagoons by rivers. Near major Tertiary igneous intrusions these depositional clay mineral assemblages have been altered. Assemblage 3 contains smectite-poor mixed-layer illite–smectite, whilst Assemblage 4 contains no smectitic clay at all. Destruction of smectite interlayers occurred at relatively shallow burial depths (< 2500 m) due to enhanced geothermal gradients and local convective hot-water circulation cells associated with the major Tertiary igneous intrusions.


Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 1-3 ◽  
Author(s):  
C. V. Jeans ◽  
R. J. Merriman

AbstractThe publication of The Clay Mineralogy of British Sediments by Perrin in 1971 collated several decades of clay mineral research in the British Isles and for the first time presented all the data in a stratigraphical framework. While it quickly became a useful source of information for geologists, engineers and soil scientists, it also revealed many gaps in clay mineral data through the geological succession, stimulating further research. Within ten years of publication, a successor to Perrin's book was under discussion by the Clay Minerals Group. Inevitably, the enthusiasm for the concept of the project gave way to the patience of a long gestation. A successor to Perrin (1971) became a standing item on the agenda of Clay Minerals Group Committee meetings, and the bane of many a Chairman's three years in office. By the mid-1990s the project began to show real progress, gathering momentum from the success of an international series of 'Cambridge clay mineral diagenesis conferences' (1981, 1984, 1986, 1989, 1993, 1998) that were supported by the oil industry. A timely injection of financial support from the Joint Association for Petroleum Exploration Courses (JAPEC) ensured a successful conclusion for the project.The cost of publication has been borne by three sponsors: the Clay Minerals Group, JAPEC (UK: training), and the Mineralogical Society. Consequently, the financing of this Special Volume of Clay Minerals is entirely independent of the usual costs of publishing the journal. We owe our particular thanks to Kevin Murphy, Editorial Manager, for his care and humour in guiding Clay minerals in onshore and offshore strata of the British Isles through publication.


Hypotheses are reviewed on the origin of the magnesium-rich Triassic clays which characterize the Germanic facies of western Europe and north Africa. Relations between clay minerals, megafacies and stratigraphy are described from 28 localities in the Triassic Keuper Marl, Tea Green Marl and Rhaetic sediments of England. Two clay mineral assemblages are recognized: (1) a detrital assemblage of mica with minor chlorite which occurs throughout all the sediments investigated, and (2) a neoformed assemblage of magnesium-rich clay minerals with a limited occurrence related to certain megafacies cycles which resulted from the transgression and regression of the Alpine facies into the Germanic facies; this assemblage includes sepiolite, palygorskite, chlorite, smectite, corrensite and irregular mixed-layer smectite/mica and smectite/chlorite minerals. The clay mineral neoformations resulted from reactions between the water masses in which the Germanic and Alpine facies were deposited. Controlling the distribution and types of minerals neoformed were the general and local variations in the chemistries of the Alpine and Germanic water masses, as well as competition for available magnesium from other mineral-forming reactions.


Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 355-393 ◽  
Author(s):  
K. Ziegler

AbstractThe nature, distribution and origin of clay minerals in the hydrocarbon-bearing Permian Rotliegend sandstones of the North Sea and the adjacent areas of the Netherlands and Germany are reviewed. The clay minerals occur as detrital coatings of smectite and smectite-illite on the surfaces of sandgrains, and as later diagenetic cements of kaolinite, chlorite (two varieties), and illite in the pore spaces of those sandstones. Two diagenetic clay mineral assemblages are predominant in the Rotliegend of the North Sea. The kaolinite-illite assemblage is restricted to the Rotliegend of shelf areas which underwent shallow burial followed by strong Jurassic/Cretaceous (Late Cimmerian) structural inversions, whereas the illite-chlorite assemblage is associated with basinal areas that underwent deep and rapid burial throughout the Mesozoic.The factors controlling mineralogy, crystal chemistry and morphology of those diagenetic clay minerals, as well as their regional distribution and origin, are numerous, complicated, and inter- related. Evidence suggests that the following aspects were important parameters: (1) variations in the original depositional arid desert environment; (2) the chemistry and flow patterns of the porewaters; (3) temperature and timing of clay mineral formation; (4) local burial history; (5) the presence or absence of meteoric water; and (6) the structural setting of the Rotliegend sandstones.Oxygen isotope data indicate that the illite cements formed over a wide range of temperatures (24–140°C) that is consistent with the deep burial conditions prevailing in the palaeo-basins. In contrast, oxygen isotopes indicate that kaolinite cements formed over a more restricted temperature range (40–80°C) and under the influence of meteoric water penetrating the sandstones of the shelf areas as a result of their Late Cimmerian uplift and associated erosion. Hypotheses suggesting that the absence of kaolinite cement from the deeply buried Rotliegend sandstones is caused by its illitization during burial, and that the chlorite cements have formed by the alteration of earlier smectite, smectite-chlorite and corrensite cements, are not supported by evidence.


Clay Minerals ◽  
2000 ◽  
Vol 35 (1) ◽  
pp. 25-55 ◽  
Author(s):  
C. V. Jeans ◽  
D. S. Wray ◽  
R. J. Merriman ◽  
M. J. Fisher

AbstractThe 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.


Clay Minerals ◽  
2002 ◽  
Vol 37 (4) ◽  
pp. 699-707 ◽  
Author(s):  
A. Mirabella ◽  
M. Egli ◽  
S. Carnicelli ◽  
G. Sartori

AbstractThe formation of clay minerals was investigated in Spodosols developed in the subalpine belt, with similar exposure, climate and age, but deriving from different parent materials. All the soils were classified as Haplic Podzols and showed the characteristic eluviation and illuviation features of Fe, Al and organic carbon. However, varying parent material lithology led to different clay mineral assemblages in the soil. Smectite could be found in the E horizons of soils developed from granodiorite and tonalite materials. Its formation was strongly dependent on the presence of chlorite in the parent material. If nearly no other 2:1 mineral components, such as chlorite, are present in the lower soil horizons, then a residual micaceous mineral becomes the dominant clay mineral. The latter derives from a mica-vermiculite interstratified mineral.


Clay Minerals ◽  
2001 ◽  
Vol 36 (3) ◽  
pp. 325-333 ◽  
Author(s):  
J. F. Barrenechea ◽  
M. Rodas ◽  
M. Frey ◽  
J. Alonso-Azcárate ◽  
J. R. Mas

AbstractThe clay mineral assemblages of the Tithonian and Berriasian sediments (Tera and Oncala Groups) in the eastern part of the Cameros basin are investigated at seven localities. The lowest-grade assemblage, located on the southern border of the basin, contains calcite + quartz + hematite + kaolinite + mixed-layer illite-smectite (R = 1, 65 85% illite layers) + discrete illite (IC = 0.5 0.65Δ°2θ). Systematic increases in the illite and chlorite crystallinities suggest increasing metamorphic grade from the northwest part of the basin to the southeast. This trend does not follow the pattern previously described for the overlying late Berriasian–early Aptian sediments (Urbión and Enciso Groups), which exhibit a higher metamorphic grade. This may result from local variations in sedimentary facies, as well as the circulation of hot migratory fluids. Tertiary compression occurring long after the main metamorphic event is considered to be responsible for the enhanced illite and chlorite crystallinities measured in the SE extreme of the basin.


Clay Minerals ◽  
2006 ◽  
Vol 41 (1) ◽  
pp. 5-46 ◽  
Author(s):  
J. M. Huggett ◽  
R. W. O'B. Knox

AbstractTertiary sediments are of restricted occurrence in the onshore British Isles but occur extensively offshore, attaining thicknesses of ~4 km in the Faroe—Shetland Basin and ~3 km in the North Sea Basin. Clay mineral stratigraphic studies of the North Sea Paleocene to Lower Miocene successions show a dominance of smectite (and smectite-rich illite-smectite) with minor illite, kaolin and chlorite. Abundant smectite in the Paleocene and Eocene reflects alteration of volcanic ash derived from pyroclastic activity associated with the opening of the North Atlantic between Greenland and Europe. However, the persistence of high smectite into the Oligocene and Middle Miocene indicates that smectite-rich soils on adjacent land areas may also have been an important source of detrital clays. An upwards change to illite-dominated assemblages in the Middle Miocene reflects higher rates of erosion and detrital clay supply, with a subsequent increase in chlorite reflecting climatic cooling. The persistence of smectite-rich assemblages to depths of >3000 m in the offshore indicates little burial-related diagenesis within the mudstone succession, possibly as a consequence of over-pressuring. Despite the importance of Paleocene and Eocene sandstones as hydrocarbon reservoirs in the North Sea and Faroe-Shetland basins, there are few published details of the authigenic clays. The principal clay cements in these sandstones are kaolin and chlorite, with only minor illite reported.The offshore successions provide a valuable background to the interpretation of the more intensively studied, but stratigraphically less complete, onshore Tertiary successions. The most extensive onshore successions occur in the London and Hampshire basins where sediments of Paleocene to earliest Oligocene age are preserved. Here clay assemblages are dominated by illite and smectite with subordinate kaolin and chlorite. The relatively large smectite content of these successions is also attributed primarily to the alteration of volcanic ash. Associated non-smectitic clays are largely detrital in origin and sourced from areas to the west, with reworking of laterites and “china clay” deposits developed over Cornish granites. Authigenic clays include glauconite (sensu lato), early diagenetic kaolin that has replaced muscovite (principally in the London Clay Formation of the London Basin) and smectite that has replaced ash. Pedogenesis has extensively modified the assemblages in the Reading Formation and Solent Group. Tertiary sediments are largely missing from onshore northern and western Britain, but clays and sands of Eocene and Oligocene age are locally preserved in small fault-bounded basins. Here, clay assemblages are dominated by kaolin with minor illite.


Clay Minerals ◽  
2009 ◽  
Vol 44 (3) ◽  
pp. 389-404 ◽  
Author(s):  
M. Setti ◽  
L. Marinoni ◽  
A. Lopez-Galindo

AbstractThe CRP-3 drilling project collected sediments from 3 to 939 mbsf (metres below sea floor) in the Victoria Land Basin in Antarctica. The upper sequence (down to ~790 m bsf) is of Cenozoic age and made up of detrital glaciogenic sediments; the characteristics of clay minerals in this part have been reported elsewhere. Here, the compositional features of clay minerals in the lower sequence such as conglomerates, Devonian sandstones and dolerites are described and genetic processes clarified. Clay minerals in the deepest part of the sequence derive from the alteration of different lithologies that mostly make up the sedimentary basin.Two clay mineral assemblages were characterized through analysis by X-ray diffraction (XRD), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). From 790 to 823 mbsf, samples consist of authigenic smectite of variable chemical composition forming imbricated texture of plates or flakes. The smectites probably result from hydrothermal/diagenetic transformation of earlier minerals. The primary smectite cement underwent reorganization during shearing and cataclasis. The lowest part of the sequence (below 823 mbsf) is characterized by an assemblage of kaolinite, mixed-layer illite-smectite, Fe oxyhydroxide, sporadic smectite and poorly crystallized illite. It reflects a stronger alteration process than that recorded in the upper units of core CRP-3, related to hydrothermalism connected with the intrusion of an igneous body. Both assemblages show clear differences in particle morphology, texture and smectite composition to the clay assemblages found in the Cenozoic glaciomarine sediments in the upper sequence. The different phases of alteration appear related to the processes of rifting, exhumation and faulting that characterized this region since the Mesozoic.


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