- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
NARROW
GeoRef Subject
-
all geography including DSDP/ODP Sites and Legs
-
Atlantic Ocean
-
North Atlantic
-
Faeroe-Shetland Basin (1)
-
North Sea (1)
-
-
-
Chalk Aquifer (1)
-
Europe
-
Central Europe
-
Czech Republic
-
Bohemian Basin (1)
-
-
Poland
-
Lodzkie Poland
-
Belchatow Poland (1)
-
-
-
-
Western Europe
-
Belgium (1)
-
United Kingdom
-
Great Britain
-
England
-
Cotswold Hills (1)
-
Gloucestershire England (1)
-
Hampshire Basin (8)
-
Hampshire England (1)
-
Isle of Wight England (10)
-
London Basin (1)
-
Sussex England (2)
-
-
Wales (1)
-
-
-
-
-
Thames River (2)
-
Trent Valley (1)
-
-
commodities
-
water resources (2)
-
-
elements, isotopes
-
carbon
-
C-13/C-12 (1)
-
-
isotope ratios (3)
-
isotopes
-
stable isotopes
-
C-13/C-12 (1)
-
O-18/O-16 (2)
-
-
-
oxygen
-
O-18/O-16 (2)
-
-
-
fossils
-
Chordata
-
Vertebrata
-
Tetrapoda
-
Mammalia
-
Theria
-
Eutheria
-
Rodentia (2)
-
-
-
-
-
-
-
Invertebrata
-
Mollusca
-
Gastropoda (2)
-
-
-
microfossils
-
Charophyta (2)
-
-
palynomorphs
-
Dinoflagellata (1)
-
megaspores (1)
-
-
Plantae
-
algae
-
Chlorophyta
-
Charophyta (2)
-
-
-
Pteridophyta
-
Filicopsida
-
Azolla (1)
-
-
-
Spermatophyta
-
Angiospermae
-
Monocotyledoneae (1)
-
-
-
-
-
geochronology methods
-
K/Ar (2)
-
optically stimulated luminescence (1)
-
-
geologic age
-
Cenozoic
-
Quaternary
-
Pleistocene (2)
-
-
Tertiary
-
Paleogene
-
Eocene
-
Bracklesham Group (1)
-
middle Eocene
-
Barton Clay (1)
-
Bartonian (1)
-
Lutetian (1)
-
-
upper Eocene
-
Priabonian (2)
-
-
-
Oligocene
-
Bembridge Marls (1)
-
lower Oligocene
-
Rupelian (1)
-
-
-
Paleocene (1)
-
-
-
-
Mesozoic
-
Cretaceous
-
Lower Cretaceous
-
Gault Clay (1)
-
Wealden (1)
-
-
Lower Greensand (1)
-
-
-
MIS 5 (1)
-
Paleozoic
-
Carboniferous (1)
-
-
Phanerozoic (1)
-
-
minerals
-
silicates
-
sheet silicates
-
clay minerals
-
kaolinite (2)
-
smectite (2)
-
-
illite (3)
-
mica group
-
glauconite (2)
-
-
-
-
-
Primary terms
-
absolute age (2)
-
Atlantic Ocean
-
North Atlantic
-
Faeroe-Shetland Basin (1)
-
North Sea (1)
-
-
-
biogeography (1)
-
carbon
-
C-13/C-12 (1)
-
-
Cenozoic
-
Quaternary
-
Pleistocene (2)
-
-
Tertiary
-
Paleogene
-
Eocene
-
Bracklesham Group (1)
-
middle Eocene
-
Barton Clay (1)
-
Bartonian (1)
-
Lutetian (1)
-
-
upper Eocene
-
Priabonian (2)
-
-
-
Oligocene
-
Bembridge Marls (1)
-
lower Oligocene
-
Rupelian (1)
-
-
-
Paleocene (1)
-
-
-
-
Chordata
-
Vertebrata
-
Tetrapoda
-
Mammalia
-
Theria
-
Eutheria
-
Rodentia (2)
-
-
-
-
-
-
-
clay mineralogy (2)
-
climate change (2)
-
crust (1)
-
diagenesis (1)
-
Europe
-
Central Europe
-
Czech Republic
-
Bohemian Basin (1)
-
-
Poland
-
Lodzkie Poland
-
Belchatow Poland (1)
-
-
-
-
Western Europe
-
Belgium (1)
-
United Kingdom
-
Great Britain
-
England
-
Cotswold Hills (1)
-
Gloucestershire England (1)
-
Hampshire Basin (8)
-
Hampshire England (1)
-
Isle of Wight England (10)
-
London Basin (1)
-
Sussex England (2)
-
-
Wales (1)
-
-
-
-
-
faults (1)
-
folds (1)
-
geochemistry (2)
-
geochronology (1)
-
geomorphology (1)
-
geophysical methods (1)
-
ground water (1)
-
hydrology (1)
-
Invertebrata
-
Mollusca
-
Gastropoda (2)
-
-
-
isotopes
-
stable isotopes
-
C-13/C-12 (1)
-
O-18/O-16 (2)
-
-
-
Mesozoic
-
Cretaceous
-
Lower Cretaceous
-
Gault Clay (1)
-
Wealden (1)
-
-
Lower Greensand (1)
-
-
-
oxygen
-
O-18/O-16 (2)
-
-
paleoclimatology (3)
-
paleoecology (2)
-
paleogeography (3)
-
Paleozoic
-
Carboniferous (1)
-
-
palynomorphs
-
Dinoflagellata (1)
-
megaspores (1)
-
-
Phanerozoic (1)
-
Plantae
-
algae
-
Chlorophyta
-
Charophyta (2)
-
-
-
Pteridophyta
-
Filicopsida
-
Azolla (1)
-
-
-
Spermatophyta
-
Angiospermae
-
Monocotyledoneae (1)
-
-
-
-
sea-level changes (5)
-
sedimentary rocks
-
carbonate rocks
-
beachrock (1)
-
limestone (1)
-
-
chemically precipitated rocks
-
flint (1)
-
-
clastic rocks
-
sandstone (1)
-
-
-
sedimentation (1)
-
sediments
-
clastic sediments
-
clay (2)
-
-
-
shorelines (1)
-
soils
-
Gleys (1)
-
-
stratigraphy (3)
-
tectonics (1)
-
water resources (2)
-
weathering (2)
-
-
sedimentary rocks
-
sedimentary rocks
-
carbonate rocks
-
beachrock (1)
-
limestone (1)
-
-
chemically precipitated rocks
-
flint (1)
-
-
clastic rocks
-
sandstone (1)
-
-
-
-
sedimentary structures
-
channels (1)
-
-
sediments
-
sediments
-
clastic sediments
-
clay (2)
-
-
-
-
soils
-
paleosols (3)
-
soils
-
Gleys (1)
-
-
Hamstead Member
( a ) Section of Hamstead Member, Bouldnor, showing Nematura Bed sharply ov...
The ‘Grande Coupure’ in the Hampshire Basin, UK: taxonomy and stratigraphy of the mammals on either side of this major Palaeogene faunal turnover
Abstract Mammals from strata immediately underlying and overlying the Grande Coupure in the Hampshire Basin, UK, are described or reviewed. Precise superposed mammaliferous horizons are documented and the stratigraphy of older less precise records is assessed. The following species group taxa are described for the first time in the UK: Amphiperatherium minutum, A. exile, Peratherium cf. perrierense, Bransatoglis planus, Butseloglis micio, Theridomys bonduelli, Isoptychus margaritae, Pseudoltinomys cuvieri, Tetracus aff. nanus, Myxomygale cf. antiqua, Hyaenodon cf. dubius, Amphicynodon? sp., Plagiolophus major and Ronzotherium cf. romani . The main systematic innovations are as follows. The post-Grande Coupure record of Perather-ium cf. perrierense shows this species to range into the Oligocene, later than its supposed descendant P. cayluxi , with which it is tentatively concluded instead to have a sister relationship. Pre-Grande Coupure Glamys fordi represents the earliest record of the species; its morphology shows no increased similarity to its primitive sister species G. devoogdi , supporting the clado-genetic model for Glamys species. Intraspecific variation and the previously unknown upper fourth deciduous premolar are documented in the rodent Theridomys bonduelli , thanks to the discovery of the first substantial assemblage of the species. A first lower premolar is tentatively recognized for the mole Myxomygale , which if correctly associated suggests placement in the tribe Scaptonychini rather than Urotrichini, where it is usually classified. If the tentative identification to M. antiqua is correct, upper teeth are recorded for the first time in this species. An ulna is tentatively attributed to the oldest known mole Eotalpa . The occurrence of Leptadapis in the upper Hamstead Member is the first post-Grande Coupure adapid and the youngest member of the family Adapidae in Europe. The recent synonymy of Elomeryx porcinus with E. crispus is discounted and the former species resurrected. Diplopus is once more considered closely related to Elomeryx and returned from the Choeropotamidae to the Anthracotheriidae. In addition to the established dental differences, the subspecies Palaeotherium muehlbergi muehlbergi is shown to be distinguished from P. m. thaleri by having a shallower narial incision. The dimensions of Plagiolophus minor from the lower Hamstead Member imply a more complex pattern of relationships with its immediate relatives than the single-lineage model so far proposed. Plagiolophus major is distinguished from P. fraasi on proportional dimensions of M 3 and tentatively on crown height and position of the preorbital fossa. Implications for European Paleogene biostratigraphy are as follows. Reference level MP20 is difficult to identify without the terminal subspecies of Palaeotherium medium and P. curtum . The upper limit of the Palaeotherium curtumfrohnstettense–P . medium suevicum Biozone in the UK is raised to a position within the Hamstead Member. A significant and eventful timespan is concluded to be represented by the lowest European reference level above the Grande Coupure (MP21), which would be best resolved by conventional biostratigraphic subdivision. The distancing of Elomeryx crispus from E. porcinus means that the former may not be an early herald of the Grande Coupure.
Rarefaction curves for mammalian assemblages from the lower fauna of the Be...
Refined correlation of the UK Late Eocene–Early Oligocene Solent Group and timing of its climate history
The dominantly nonmarine Solent Group of the Hampshire Basin, southern England, spans the Late Eocene and earliest Oligocene. It contains a rich biota, including mammals and charophytes, but contains few fully marine, time-diagnostic intervals. Correlation with standard marine successions is provided here using bio-stratigraphically significant mammals and charophytes via interdigitation of strata with those containing marine zonal indicators or via magnetostratigraphy in other parts of Europe. This allows the re-identification of recently described normal polarity intervals in the Solent Group to magnetochrons C16n, 15n, 13r1n, and 13n, and improved calibration of the Solent Group to the geomagnetic polarity time scale (GPTS). Consistent with this calibration, interpreted Solent Group sea-level changes can be related to those recognized to be global in deep-marine successions in central Italy. The major sea-level fall associated with polar ice buildup at the Oligocene isotope event Oi-1 near the beginning of the Oligocene is shown to be represented in the Hamstead Member of the Bouldnor Formation by the falling stage systems tract followed by a major hiatus before the next maximum flooding surface. This hiatus encompasses the large European mammalian faunal turnover known as the “Grande Coupure.” Improved calibration to the GPTS allows better dating of climate proxies, such that recently described summer freshwater temperatures can be shown to track global fluctuations across the Eocene-Oligocene transition.
Eocene–Oligocene mammalian faunal turnover in the Hampshire Basin, UK: calibration to the global time scale and the major cooling event
Range chart of mammalian species-group taxa in the Hampshire Basin from the...
Discussion on the Eocene–Oligocene boundary in the UK Journal , Vol. 163, 2006, pp. 401–415
Possible correlations to the Geomagnetic Polarity Time Scale (GPTS, calibra...
Summer temperatures of late Eocene to early Oligocene freshwaters
Coupling of marine and continental oxygen isotope records during the Eocene-Oligocene transition
Correlation of Eocene–Oligocene marine and continental records: orbital cyclicity, magnetostratigraphy and sequence stratigraphy of the Solent Group, Isle of Wight, UK
Sample locations and their stratigraphic context. The extent of sections se...
Use of high-resolution stratigraphy and derived lithoclasts to document structural inversion: a case study from the Paleogene, Isle of Wight, UK
Morphological Evolution of Stratiotes through the Paleogene in England: An Example of Microevolution in Flowering Plants
Indicative meanings of geological sea-level indicators in the Solent region and Sussex coast (south coast of England) and implications for uplift rates
An assessment of the ability to derive regional resistivity maps from geological mapping data
Abstract The Hampshire Basin was first characterized by Prestwich (1847a, b) as a tectonic/depositional feature (as the ‘Isle of Wight Basin ’). It is an east-west-orientated, broadly synclinal but asymmetrical structure, within which are smaller similarly orientated folds, preserving up to 800 m of Paleogene strata. It extends from southern England into the eastern English Channel (Figs 42, 135 & 136). It is limited in the south by the steep, en echelon monoclinal Purbeck 2 Isle of Wight folds. Upper Paleocene-lowest Oligocene strata are represented. Upper Eocene and Early Oligocene strata are preserved only in the northern half of the Isle of Wight and adjacent areas of SW Hampshire. The coastal cliff and foreshore exposures in the Hampshire Basin, particularly in the Isle of Wight, are the most extensive Paleogene sections in NW Europe, and have been studied since the late eighteenth century. Many other exposures and boreholes, including deep holes drilled for petroleum exploration, have contributed to the database. Recent remapping of large areas by the British Geological Survey (BGS), including several deep cored boreholes, has enabled a comprehensive revised stratigraphic framework for much of the succession (Edwards & Freshney 1987a, b; Insole & Daley 1985; Daley 1999; Daley & Balson 1999; King 2006).
Clay mineralogy of the Tertiary onshore and offshore strata of the British Isles
A review of hydrogeology and water resources on the Isle of Wight
Abstract The most important onshore Paleogene deposits of Britain are the classic sequences of the London and Hampshire basins, SE England, which have been studied almost since the first interest in rocks and fossils developed in this country. Ostracods were identified and reported from these sequences relatively early (e.g. Jones 1854 ), following shortly after the key stratigraphical works of Joseph Prestwich published between 1846 and 1855, although not as early as continental workers recorded Cenozoic ostracods (e.g. Minster 1830). At the time of writing the authors are not aware of any significant published records of British Paleogene Ostracoda from outside the classic onshore sequences of SE England, and the present chapter primarily concerns that region. However, the occurrence of ostracods in offshore basins is briefly reviewed below.