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  • Result 1-8 of 8
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1.
  • Álvaro, J. Javier, et al. (author)
  • Global Cambrian trilobite palaeobiogeography assessed using parsimony analysis of endemicity
  • 2013
  • In: Early Palaeozoic Biogeography and Palaeogeography. - 0435-4052. - 9781862393738 ; Memoir 38:38, s. 273-296
  • Book chapter (peer-reviewed)abstract
    • Palaeobiogeographical data on Cambrian trilobites obtained during the twentieth century are combined in this paper to evaluate palaeoceanographic links through c. 30 myr, once these arthropods biomineralized. Worldwide major tectonostratigraphic units are characterized at series intervals of Cambrian time and datasets of trilobite genera (629 for Cambrian Series 2, 965 for Cambrian Series 3, and 866 for the Furongian Series) are analysed using parsimony analysis of endemicity. Special attention is given to the biogeographical observations made in microcontinents and exotic terranes. The same is done for platform-basinal transects of well-known continental margins. The parsimony analysis of endemicity analysis resulted in distinct palaeogeographical area groupings among the tectonostratigraphic units. With these groupings, several palaeobiogeographical units are distinguished, which do not necessarily fit the previously proposed biogeographical realms and provinces. Their development and spatial distributions are broadly controlled by Cambrian palaeoclimates, palaeogeographical conditions (e.g. carbonate productivity and anoxic conditions) and ocean current circulation.
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2.
  • Eriksson, Mats, et al. (author)
  • Ordovician and Silurian polychaete diversity and biogeography
  • 2013
  • In: Early Palaezoic Biogeography and Palaeogeography. - 0435-4052. ; :38, s. 265-272
  • Conference paper (peer-reviewed)abstract
    • Eunicidan polychaetes formed a significant part of Early Palaeozoic marine invertebrate communities, as shown by the abundance and diversity of scolecodonts (polychaete jaws) in the fossil record. In this study we summarize the early radiation and biodiversity trends and discuss the palaeobiogeography of these fossils. The oldest (latest Cambrian-Early Ordovician) representatives had primitive, usually symmetrical, placognath/ctenognath type jaw apparatuses. The first more advanced taxa, possessing labidognath-type jaw apparatuses or placognath apparatuses with compound maxillae, are first recorded in the Middle Ordovician. The most significant increase in generic diversity occurred in the Darriwilian, when many common taxa appeared and diversified. The Ordovician and Silurian scolecodont occurrences allow some palaeobiogeographical units and distribution patterns to be explored and outlined. The most robust data presently at hand derive from successions in Baltica and Laurentia. That information, together with new records from other palaeocontinents, reveals a wide distribution for the most frequent and species-rich genera and families, similar to the biogeographical patterns of extant polychaetes. Like many other benthic and pelagic fossil groups, scolecodont-bearing polychaetes show an increased cosmopolitan character in the Silurian as compared with the Ordovician. Species-level endemism appears to be relatively common, inferring a potential for scolecodonts as biogeographical tools in the future.
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  • Gee, David G., et al. (author)
  • Middle thrust sheets in the Caledonide orogen, Sweden: the outer margin of Baltica, the continent–ocean transition zone and late Cambrian–Ordovician subduction–accretion
  • 2020
  • In: Sweden. - : Geological Society of London. - 9781786204608 ; 50:1, s. 517-548
  • Book chapter (other academic/artistic)abstract
    • Nappes of continental outer and outermost margin affinities (Middle Allochthon) were transported from locations west of the present Norwegian coast and thrust eastwards onto the Baltoscandian foreland basin and platform. They are of higher metamorphic grade than underlying thrust sheets and most are more penetratively deformed. These allochthons are treated here in three groups. The lower thrust sheets comprise Paleoproterozoic crystalline basement (e.g. Tännäs Augen Gneiss Nappe) and greenschist facies, Neoproterozoic, siliciclastic metasedimentary rocks (e.g. Offerdal Nappe). These are overthrust by a Cryogenian−Ediacaran succession intruded by c. 600 Ma dolerites (Baltoscandian Dyke Swarm) with an affinity to mid-ocean ridge basalt containing normal to enriched incompatible element contents (Särv Nappes). The upper sheets are dominated by higher-grade allochthons (Seve Nappe Complex) with similar, mainly siliciclastic sedimentary protoliths, more mafic magmatism and some solitary ultramafic bodies. Within this early Ediacaran continent−ocean transition zone (COT) assemblage, generally metamorphosed in amphibolite facies, some nappes experienced migmatization, and eclogites are present. Evidence of ultrahigh-pressure metamorphism has been obtained from garnet peridotites and eclogites; recently, microdiamonds have been discovered in paragneisses. Subduction of the COT started by the late Cambrian and accretion continued through the Ordovician, prior to the Baltica–Laurentia collision. Thrusting of all these Middle allochthons onto the foreland basin exceeds a distance of 400 km.
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5.
  • Harper, David A. T., et al. (author)
  • Biodiversity, biogeography and phylogeography of Ordovician rhynchonelliform brachiopods
  • 2013
  • In: EARLY PALAEOZOIC BIOGEOGRAPHY AND PALAEOGEOGRAPHY. - 0435-4052. ; :38, s. 127-144
  • Conference paper (peer-reviewed)abstract
    • The phylogeographical evolution and the consequent changing distribution and diversity of rhynchonelliform brachiopods through the Ordovician are linked to the dynamic palaeogeography of the period. The Early Ordovician (Tremadocian and Floian) is characterized by globally low-diversity faunas with local biodiversity epicentres, notably on the South China Palaeoplate; low-latitude porambonitoid-dominated faunas with early plectambonitoid and clitambonitoid representatives, as well as high-latitude assemblages mostly dominated by orthoids, can be recognized, but many taxa are rooted in Late Cambrian stocks. The Early Ordovician displays a steady increase in rhynchonelliformean biodiversity, which was mostly driven by the increasing success of the Porambonitoidea and Orthoidea, but the billingsellids and early plectambonitoids also contributed to this expansion. During the Early to Mid Ordovician (Dapingian-Darriwilian), marine life experienced an unprecedented hike in diversity at the species, genus and family levels that firmly installed the suspension-feeding benthos as the main component of the Palaeozoic fauna. However, this may have occurred in response to an early Darriwilian annihilation of existing clades, some of which had been most successful during the Early Ordovician. New clades rapidly expanded. The continents were widely dispersed together with a large number of microcontinents and volcanic arcs related to intense magmatic and tectonic activity. Climates were warm and sea-levels were high. Pivotal to the entire diversification is the role of gamma (inter-provincial) diversity and by implication the spread of the continents and frequency of island arcs and microcontinents. The phylogeographical analysis demonstrates that this new palaeogeographical configuration was particularly well explored and utilized by the strophomenides, especially the Plectambonitoidea, which radiated rapidly during this interval. The porambonitoids, on the other hand, were still in recovery following the early Darriwilian extinctions. Orthides remained dominant, particularly at high latitudes. Biodiversity epicentres were located on most of the larger palaeoplates, as well as within the Iapetus Ocean. Provincial patterns were disrupted during the Sandbian and early Katian with the migration of many elements of the benthos into deeper-water regimes, enjoying a more cosmopolitan distribution. Later Katian faunas exhibit a partition between carbonate and clastic environments. During the latest Katian, biogeographical patterns were disrupted by polewards migrations of warm-water taxa in response to the changing climate; possibly as a consequence of low-latitude cradles being developed in, for instance, carbonate reef settings. Many clades were well established with especially the strophomenides beginning to outnumber the previously successful orthides, although this process had already begun, regionally, in the mid to late Darriwilian. At the same time, atrypoid and pentameroid clades also began to radiate in low-latitude faunas, anticipating their dominance in Silurian faunas. The Hirnantian was marked by severe extinctions particularly across orthidestrophomenide clades within the context of few, but well-defined, climatically controlled provincial belts.
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8.
  • Zigaite, Zivile, et al. (author)
  • Palaeobiogeography of Early Palaeozoic vertebrates
  • 2013
  • In: Early Palaeozoic Biogeography and Palaeogeography. - London. - 9781862393738 ; 38:1, s. 449-460
  • Conference paper (peer-reviewed)abstract
    • The oldest known Palaeozoic vertebrate record currently is Early Cambrian in age. The first taxa with mineralized exoskeletons are at least Ordovician in age, followed by a sporadic fossil record with Talimaa’s Gap of c. 3 myr in the Rhuddanian (earliest Silurian). Ordovician and Silurian vertebrate faunas are dominated by ‘agnathans’. Early Palaeozoic vertebrates occupied a wide range of environments: nearshore marine to restricted marine in the Ordovician, and on the marine epicontinental shelves of the Silurian. Silurian vertebrates are useful biostratigraphical indicators, as well as good markers of palaeocontinental margins. Two main palaeobiogeographical units are renamed for the Ordovician: a Gondwana Realm and a Laurentia–Siberia–Baltica Realm. Vertebrate fossil localities are more numerous in the Silurian; therefore a series of palaeobiogeographical provinces and realms are defined on Laurentia, Baltica, Avalonia, Siberia, South China and East Gondwana. More discoveries of Silurian vertebrate-bearing localities should certainly help to define additional provinces, in particular along the northern margins of Gondwana and in SE Asia.
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  • Result 1-8 of 8

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