The 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.

Tertiary 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.

The clay mineralogy of the Cretaceous strata of the British Isles is described and discussed within its lithostratigraphical and biostratigraphical framework using published and unpublished sources as well as 1400 new clay mineral analyses. The regional clay mineral variation is described systematically for the following strata:

1. (1) Southern England — Purbeck Limestone Group (Berriasian/Ryazanian; Lulworth and Durlston formations), Wealden Group (Valanginian—Barremian/Aptian; Ashdown, Wadhurst Clay, Tunbridge Wells Sands, Grinstead Clay Member, Wealden Clay, Wessex and Vectis formations), Lower Greensand (Aptian—Lower Albian; Atherfield Clay, Hythe, Sandgate, Folkestone Sands, Ferruginous Sands, Woburn Sands and Faringdon Sponge Gravels formations), Selborne Group (Middle—Upper Albian; Gault Clay and Upper Greensand formations) and the Chalk Group (Cenomanian—Lower Maastrichtian).

2. (2) Eastern England — Cromer Knoll Group (Ryazanian—Upper Albian; Speeton Clay, Spilsby Sandstone, Sandringham Sands, Claxby Ironstone, Tealby, Roach Ironstone, Dersingham, Carstone and Red Chalk (or Hunstanton Red Limestone) formations).

3. (3) Scotland — Inner Hebrides Group (Cenomanian—Campanian; Morvern Greensand, Gribun Chalk, Coire Riabhach Phosphatic Hibernian Greensands formations).

4. (4) Northern Ireland — Hibernian Greensands (Cenomanian—Santonian) and Ulster White Limestone formations (Santonian—Lower Maastrichtian).

The stratigraphical patterns of clay mineral variation divide naturally into two types; firstly, the more complex pattern of the Lower Cretaceous strata and secondly, the simple pattern of the Upper Cretaceous. Clay mineral variations in the non-marine and marine Lower Cretaceous strata of England are best explained by the interplay of two main clay mineral assemblages between which all gradations occur. The assemblage which dominates the main clay formations consists of mica, kaolin and poorly defined mixed-layer smectite-mica-vermiculite minerals, and sometimes includes vermiculite and traces of chlorite. It is dominantly of detrital origin and detailed evidence indicates it is derived largely from the reworking of Mesozoic sediments although ultimately from weathered Palaeozoic sediments and metasediments. Although mainly of detrital origin, this assemblage contains a persistent component that formed coevally with the approximate depositional age of its host sediment. Whether this component is of soil origin or was neoformed in the sediment shortly after deposition is unclear. There is little firm evidence indicating the sources of this clay mineral detritus. However, in the strata of the Wealden Group of southern England, mineral trends suggest three sources; one of these was to the west (Cornubian Massif), another must have been the Anglo- Brabant landmass. In the Selborne Group (Middle—Upper Albian) and in the overlying Lower Chalk (Cenomanian) where this assemblage makes its last appearance in the Cretaceous of England, there is good evidence of easterly and south-easterly sources.

The second main assemblage tends to be largely monominerallic, and usually dominated by smectite with or without small amounts of mica; less frequently, kaolin, berthierine or glauconite sensu lato is the sole or dominant component. It is considered to be of volcanogenic origin, derived from the argillization of volcanic ash under different conditions of deposition and diagenesis. The source of the ash in Berriasian—Aptian times seems to have been an extensive volcanic field in the southern part of the North Sea and in the Netherlands, whereas in the Albian (and extending into the Cenomanian) a westerly source dominated. The current controversy about the role of climate or pattern of volcanic activity controlling the clay mineral stratigraphy of the Lower Cretaceous is reviewed.

In the lower part of the Upper Cretaceous strata of England, Scotland and Ireland, sand-grade glauconite is particularly abundant. Much of it represents the glauconitization of pene- contemporanous volcanic ash, possibly of basaltic origin, associated with continental breakup and the opening up of the Atlantic Ocean and the earliest stages in the development of the Hebridean Tertiary Igneous Province. The Upper Cretaceous Chalk facies of England and Ireland is dominated by a smectite-rich clay assemblage containing mica, and the various hypotheses for its origin (detrital, neoformation, volcanogenic) are reviewed in the light of available mineralogical, chemical and geological data.

The principal clays of the northern and central North Sea are illite (sometimes with interlayered smectite) and kaolin. Chlorite is only locally important. Although it has been proposed that kaolin within North Sea sandstones is detrital in origin, the majority of workers have concluded that it is authigenic, largely the product of feldspar alteration. Kaolin is found within a wide range of sedimentary settings (and within shales) apparently defying the notion that kaolin is an indicator of meteoric water deposition. Within sandstones, the earliest authigenic kaolin has a vermiform morphology, the distribution of which is controlled by the availability of detrital mica to act as a nucleus, and the composition of the post-depositional porewaters. This vermiform kaolin formed in meteoric water, the presence of which is easily accounted for below sub-aerial exposure surfaces in non-marine formations, and below unconformities over marine units. In fully marine sands, and even marine shale units, kaolin still occurs. It has therefore been suggested that even these locations have been flushed with meteoric water.

Early vermiform kaolin recrystallizes to a more blocky morphology as burial proceeds, at least in the Brent Group. Blocky kaolin has been reported as growing before, synchronously with, and after the formation of quartz overgrowths, though oxygen isotope studies support low-temperature growth, pre-quartz. Blocky kaolin may form during meteoric flushing associated with lower Cretaceous uplift and erosion, though it is found in fault blocks that are thought to have remained below sea level. Here, the kaolin may form in stagnant meteoric water, relics of the post-depositional porewater. It has also been proposed that the blocky kaolin grew in ascending basinal waters charged with carboxylic acids and CO2, though this hypothesis is not supported by stable oxygen isotope data. Some of the blocky kaolin is dickite, the stable polymorph above ∼100°C.

Fibrous illite occurs almost ubiquitously within the clastic sediments of the North Sea. An early pore-lining phase has been interpreted as both infiltrated clastic clay, and as an early diagenetic phase. Early clays may have been quite smectite-rich illites, or even discrete smectites. Later, fibrous illite is undoubtedly neoformed, and can degrade reservoir quality significantly. Both within sandstones and shales, there is an apparent increase in the K content deeper than 4 km of burial, which could be due to dilution of the early smectite-rich phase by new growth illite, or to the progressive illitization of existing I-S. Much of the ‘illite’ that has been dated by the K-Ar method may therefore actually be I-S.

The factors that control the formation of fibrous illite are only poorly known, though temperature must play a role. Illite growth has been proposed for almost the entire range of diagenetic temperatures (e.g. 15–20°C, Brent Group; 35–40°C, Oxfordian Sand, Inner Moray Firth; 50–90°C, Brae formation; 100–110°C, Brent Group; 130–140°C, Haltenbanken). It seems unlikely that there is a threshold temperature below which illite growth is impossible (or too slow to be significant), though this is a recurring hypothesis in the literature. Instead, illite growth seems to be an event, commonly triggered by oil emplacement or another change in the physiochemical conditions within the sandstone, such as an episode of overpressure release. Hence fibrous illite can grow at any temperature encountered during diagenesis.

Although there is an extensive dataset of K-Ar ages of authigenic illites from the Jurassic of the North Sea, there is no consensus as to whether the data are meaningful, or whether the purified illite samples prepared for analysis are so contaminated with detrital phases as to render the age data meaningless. At present it is unclear about how to resolve this problem, though there is some indication that chemical micro-analysis could help. It is a common belief that illite ages record the timing of oil charge, and so can be used to calibrate basin models.

Grain-coating Fe-rich chlorite cements can preserve exceptional porosity during burial. They are found in marginal marine sandstones, formed during diagenesis from precursor Fe-rich clays such as berthierine or verdine.

The 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.

The 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.

The 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.

The Carboniferous in Britain is diverse and this is reflected in the clay mineral assemblages. Several factors affecting the assemblages are identified including climate, rates of weathering and erosion, source rocks in the hinterland, preservation of palaeosols, whether the source rocks are nearby or distant, sorting during transportation, the presence of altered volcanic ash-falls in the depositional environment and the extent of burial diagenesis. There are temporal and geographic variations in the clay mineral assemblages in the mudrocks as a result of these controls. There are also clay-rich rocks that differ from the normal mudrocks and a knowledge of the clay mineralogy of these is a necessary prerequisite to a full understanding of their origins. Mudrocks falling in this category, and described below, include bauxitic clays, flint clays, fragmental clay rocks, tonsteins and K-bentonites and various palaeosols.

The distribution and origin of clay minerals in Carboniferous sandstone reservoir rocks, onshore and offshore UK, is reviewed using both published and unpublished sources. The clay mineralogy for many of the Carboniferous reservoir sands tends to be similar, with the detrital clays predominantly illitic whereas the diagenetic clay assemblages are dominated by kaolin with usually lesser amounts of illite. The main exception to this pattern is found in the Dinantian sandstones of the Clair Basin where significant amounts of smectite are present. Three stages of diagenetic kaolin formation are widely recognized. Firstly eogenetic and/or telogenetic kaolinite; secondly mesogenetic kaolin; and thirdly the partial or complete transformation of kaolinite to dickite during deep burial. In addition to the formation of diagenetic clay phases, the sandstone reservoirs also display a complex diagenetic history involving cementation and dissolution processes. These have affected the reservoir properties of the sandstones but the depositional facies architecture still exerts a major recognizable influence on reservoir porosity-permeability characteristics. The abundance of kaolin cements shows no clear correlation with variations in porosity and permeability for Carboniferous reservoirs. Pore- filling smectite affects reservoir porosity and permeability in the Dinantian of the Clair Field, and could be a potential source of serious reservoir damage arising from swelling.

The Devonian sedimentary rocks of the UK are made up of a continental red bed facies, the Old Red Sandstone (ORS), and sediments of a marine origin. The latter are confined to southwest England whereas the ORS occurs much more extensively, particularly in South Wales, the West Midlands, Northern England, the Midland Valley of Scotland and the Orcadian basin. The ORS also occurs extensively offshore where it contains important hydrocarbon reservoirs. Highly variable suites of clay mineral assemblages are characteristic of the ORS. In the West Midlands and Monmouthshire, the Downton Group is characterized by illitic, smectitic, and mixed-layer illite-smectite minerals. A tuff bed (Townsend Tuff) also contains expansible minerals but when the bed is traced westwards it is found that the clay mineralogy changes progressively to an illite-chlorite assemblage, suggesting the influence of diagenetic or metamorphic change. It is not known, however, whether such a transformation is typical of the Downton Group as a whole. The overlying Ditton Group in its eastern outcrops contains a high-spacing mineral identified as tosudite, together with regularly interstratified illite-smectite and well crystallized kaolinite. Further west this assemblage gives way to illite and chlorite, with the latter being trioctahedral or dioctahedral, while in Dyfed the Ditton Group may contain smectite and poorly crystallized kaolinite in addition to illite and chlorite. The geographical distribution of clay minerals in the Ditton Group may also be accounted for by progressive diagenetic to low-grade metamorphic reactions, although it is necessary to postulate retrogressive diagenesis to account for the smectite and kaolinite that occur in the Dyfed samples. The clay mineralogy of the overlying Brecon Group and the Upper ORS also consists of mixtures of illite and chlorite in the west and central parts of the region. No data are available for the Brecon Group in the eastern parts of the outcrop but the Upper ORS from around Monmouth and Portishead contains assemblages rich in kaolinite and mixed-layer illite-smectite with only minor amounts of chlorite. The distribution of clay minerals in the Upper ORS is again suggestive of a progressive westerly increase in the influence of diagenetic alteration, although the influence of provenance cannot be discounted.

In Scotland the clay mineralogy of the Lower ORS in the Midland valley is characterized by a variety of interstratified minerals, including regularly interstratified trioctahedral chlorite-vermiculite, a tosudite mineral similar to that described from South Wales and illite-smectite, as well as occasional illite, chlorite and smectite. The oldest Stonehaven Group is kaolinitic but in the younger groups kaolinite is either completely absent or present in only minor amounts. It is clear that detrital inputs, particularly from associated volcanic rocks, have contributed to the clay minerals found in these rocks, although the contribution could be indirect with diagenetic clay minerals forming from volcanic detritus after deposition. Diagenetic alteration may also be important, particularly with respect to the origin of the tosudite mineral. The Middle ORS lacustrine sediments of the Orcadian Basin of Scotland are characterized by mixtures of trioctahedral chlorite and dioctahedral illite, with interstratified chlorite-smectite, illite-smectite, kaolinite and occasional reports of minor montmorillonite. The most recent interpretations of the origins of the clay minerals in these rocks emphasize the role of progressive diagenetic and low-grade metamorphic reactions, based on correlations of clay mineral assemblages and parameters such as illite crystallinity with organic maturation data. This interpretation argues that the illite-smectite in the shales is derived largely from a precursor detrital smectite. However, the finding of two populations of morphologically and structurally distinct illite-smectite particles in the Middle and Upper ORS sandstones suggests a more complex picture involving different diagenetic episodes. In addition, the likelihood of a smectitic-rich detrital input to the ORS may also be a point of debate. The clay mineralogy of the North Sea offshore is also described briefly, in addition to the marine Devonian in southwest England. The latter is characterized by chlorite and illite assemblages of low-grade metamorphic origin, although smectite and kaolinite are also found occasionally in these rocks. The offshore ORS, however, contains a variety of clay minerals, including an assemblage similar to that found in the Lower ORS south of the Highland Boundary Fault and notably contains a tosudite-like mineral.

Lower Palaeozoic rocks crop out extensively in Wales, the Lake District of northern England and the Southern Uplands of Scotland; they also form the subcrop concealed beneath the English Midlands and East Anglia. These mainly marine sedimentary rocks were deposited in basins created during plate tectonic assembly of the various terranes that amalgamated to form the British Isles, 400-600 Ma ago. Final amalgamation occurred during the late Lower Devonian Acadian Orogeny when the basins were uplifted and deformed, producing belts of cleaved, low-grade metasediments, so-called slate belts, with a predominantly Caledonian (NE-SW) trend. The clay mineralogy of mudrock lithologies - including mudstone, shale and slate - found in these belts is reviewed. Using X-ray diffraction data from the <2 μm fractions of ~4500 mudrocks samples, clay mineral assemblages are summarized and discussed in terms of diagenetic and low-grade metamorphic reactions, and the metapelitic grade indicated by the Kübler index of illite crystallinity.

Two sequences of clay mineral assemblages, or regional assemblages, are recognized. Regional Assemblage A is characterized by a greater diversity of clay minerals in assemblages from all metapelitic grades. It includes K-rich, intermediate Na/K and Na-rich white micas, chlorite and minor amounts of pyrophyllite. Corrensite, rectorite and pyrophyllite are found in the clay assemblages of contact or hydrothermally altered mudstones. K-white micas are aluminous and phengite-poor, with b cell dimensions in the range 8.98-9.02 Å. Regional Assemblage B has fewer clay minerals in assemblages from a range of metapelitic grades. Phengite-rich K-mica is characteristic whereas Na- micas are rare, and absent in most assemblages; chlorite is present and minor corrensite occurs in mudrocks with mafic-rich detritus. Minor amounts of kaolinite are sporadically present, but dickite and nacrite are rare; pyrophyllite and rectorite are generally absent. The b cell dimensions of K-white mica in Regional Assemblage B are in the range 9.02-9.06 Å. The two regional assemblages are found in contrasting geotectonic settings. Regional Assemblage A is characteristic of the extensional basin settings of Wales, the northern Lake District and the Isle of Man. These basins have a history of early burial metamorphism associated with extension, and syn-burial or post-burial intrusive and extrusive volcanic activity. Intermediate Na/K mica probably developed from hydrothermal fluids generated around submarine volcanic centres. Deep diagenetic and low anchizonal clay mineral in these basins may develop a bedding-parallel microfabric. Chlorite-mica stacks also occur in the extensional basins and the stacking planes represent another type of bedding-parallel microfabric. Both types of microfabric are non-tectonic and developed by burial during the extensional phase of basin evolution. Regional Assemblage B is developed in the plate-convergent settings of the Southern Uplands and the southern Lake District. In the accretionary complex of the Southern Uplands the processes of burial diagenesis, metamorphism and tectonism were synchronous events. In both plate- convergent basins, low temperatures and tectonic fabric-formation had an important role in clay mineral reactions, whereas hydrothermal fluids played no part in clay genesis.