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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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United States
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Oklahoma
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Carter County Oklahoma (1)
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Utah (1)
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fossils
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Chordata
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Vertebrata (1)
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Invertebrata
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Arthropoda
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Trilobitomorpha
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Trilobita (1)
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microfossils
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Conodonta (1)
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geologic age
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Paleozoic
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Cambrian (1)
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Ordovician
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Middle Ordovician
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Darriwilian (1)
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Primary terms
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Chordata
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Vertebrata (1)
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Invertebrata
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Arthropoda
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Trilobitomorpha
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Trilobita (1)
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Paleozoic
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Cambrian (1)
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Ordovician
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Middle Ordovician
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Darriwilian (1)
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United States
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Oklahoma
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Carter County Oklahoma (1)
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Utah (1)
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rock formations
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Oil Creek Formation (1)
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Silicification of trilobites and biofilm from the Cambrian Weeks Formation, Utah: Evidence for microbial mediation of silicification: COMMENT
Regional synthesis of the Ordovician geology and stratigraphy of China
Abstract China presently comprises several independent tectonic palaeoplates or terranes and parts of other blocks, which have been assembled over geological time. In the Ordovician, these blocks included South China, North China, Tarim, Qaidam, Junggar, Qiangtang-Qamdo, Lhasa and partially Himalaya, Sibumasu and Indochina, as well as the Altay-Xing'an and Songpan-Garze fold belts, which were discrete but near-adjacent. Twelve stratigraphic megaregions bounded by tectonic sutures or major fault zones can be recognized. Some of them are further differentiated into several regions according to the lithological and biotic facies or distinct stratigraphic sequences. Here, the palaeontologic features and biostratigraphic framework of these stratigraphic megaregions and regions are summarized. The unified biostratigraphic framework presented herein is supported by 33 graptolite biozones and 27 conodont biozones, together with supplementary biozones, communities or associations of brachiopods, trilobites, cephalopods, chitinozoans, acritarchs and radiolarians. With constraints of integrative chronostratigraphy, biostratigraphy, chemostratigraphy, cyclostratigraphy and magnetostratigraphy, along with some geochronologic data, our understanding of the temporal and spatial distribution of the Ordovician lithostratigraphic units on these major blocks has been significantly advanced. Vast amounts of new data accumulated in recent decades also constrain the major Ordovician geological and biotic events evident in China, such as marine anoxia, faunal turnovers and tectonic orogenies.
Abstract Evidence of Early Ordovician deposition and intrusion in East Antarctica is best known from the Ross Orogen, postdating the 495–489 Ma Ross Orogeny. Here, c. 490–475 Ma granites (with related dykes and sills) of the Granite Harbour Intrusives represent roots of a continental margin arc. Detrital zircon grains in the upper Byrd Group (Central Transantarctic Mountains) are of comparable Early Ordovician age. Contemporaneous fossils are rare. In northern Victoria Land they include latest Cambrian to earliest Ordovician conodonts and microbrachiopods in allochthonous limestones of the Handler Formation (Robertson Bay Group) in the Robertson Bay Terrane, and probable Early Ordovician trace fossils in the Camp Ridge Quartzite of the Leap Year Group in the Bowers Terrane. In the Shackleton Range of Coats Land, West Antarctica, the Blaiklock Glacier Group contains a diverse ichnofossil fauna of probable Ordovician age associated with undescribed bivalved arthropods and segmented crustacea. The Swanson Formation of the Ross Province in Marie Byrd Land (correlated with the Robertson Bay Group of the Ross Orogen) is a turbiditic unit dominated by quartz-rich sandstones. Its Ordovician age is based on a post-depositional whole rock K–Ar metamorphic age of 448–444 Ma, with detrital zircon grains indicating a late Cambrian maximum depositional age.
The Ordovician System in Australia and New Zealand
Abstract The stratigraphic overview presented in this chapter substantially updates and revises the last major review of the Ordovician rocks of Australia and New Zealand published 40 years ago. In the western two-thirds of the present-day continent of Australia, Ordovician sedimentary rocks are restricted to intracratonic basins. The Canning Basin (Western Australia) and Amadeus Basin (central Australia) contain the best known Lower and Middle Ordovician shallow marine successions. The eastern third of the continent, known as the Tasmanides, comprises multiple orogens (i.e. Delamerian, Lachlan, New England, Thomson, Mossman) that formed along the convergent East Gondwana Margin. As a result, volcanic and intrusive rocks are much more common in these orogens than in the intracratonic basins. Their deep-water depositional environments span 31 graptolite biozones. Slope and basinal siliceous sedimentary rocks are constrained by a newly defined set of 12 conodont biozones, complementing the conodont biostratigraphic scheme refined for shallow-water environments from the basal boundary of the Ordovician to the latest Katian. In some places, these conodont biozones are integrated with radiometric ages from tuff interbeds (e.g. Canning Basin). Ordovician graptolitic strata in the Buller Terrane of New Zealand share palaeogeographic links with those in the Bendigo Zone of the western Lachlan Orogen.
Abstract Owing to the increasing availability of data for many fossil groups and a generally accepted palaeogeographical configuration, palaeontologists have been able to develop progressively more robust palaeobiogeographical scenarios for the spatial distributions of Ordovician marine faunas. However, most research in Early Paleozoic palaeobiogeography centres on data derived from extensively studied localities in North America and Europe. Thus, clear patterns are emerging of regional biogeography for these areas. However, the fragmentary nature of data from other regions hinders the development of a detailed understanding of palaeogeographical schemes of many clades at the global level. Provincial patterns are now available for several fossil groups, but the global coverage remains generally fragmentary. Palaeobiogeographical investigations were traditionally focused on better understanding of palaeogeographical scenarios and often employed quantitative analyses of faunal similarity. More recently palaeobiogeographical analyses have expanded to investigate questions such as the location and pace of speciation and macroevolution together with macroecological change. For example, studies on the evolution of speciation levels in the frame of the taxonomic radiation of the Great Ordovician Biodiversification are now available. Future investigations, including modelling, will provide more integrative, global patterns of provincialism, including the location of Ordovician biodiversity hotspots and the recognition of latitudinal diversity gradients.