Silicified brachiopods from Hirnantian strata in three sections of the lower Whittaker Formation, Mackenzie Mountains, northwestern Canada, yielded a moderately diverse, Edgewood-type Hirnantian fauna, consisting of 13 species: Biparetis paucirugosus, Brevilamnulella laevis, Dalmanella edgewoodensis, Drabovia noixella, Eospirigerina putilla, Epitomyonia paucitropida, Epitomyonia sekwiensis, Glyptorthis papillosa new species, Gnamptorhynchos orbiculoidea, Katastrophomena mackenzii new species, K. parvicardinis, Parastrophina cf. P. minor, and Skenidioides sp. Compared to the typical Edgewood fauna of the American Midcontinent, Brevilamnulella laevis has a notably smaller shell than B. thebesensis, and is interpreted as a deeper-water form. The strong faunal affinity of the Mackenzie Mountains fauna to the Edgewood-type Hirnantian fauna is indicated by the occurrence of Biparetis, Brevilamnulella, Eospirigerina, and Gnamptorhynchos. In addition to the Edgewood type area within Laurentia, Biparetis, Eospirigerina, and Gnamptorhynchos are characteristic taxa that also occur in the Ellis Bay Formation (Hirnantian) of Anticosti Island. Multivariate and network analyses strongly support the differentiation between an Edgewood-type Hirnantian fauna in Laurentia and peri-Laurentia and the typical Hirnantia fauna of the Kosov Province in Gondwana, peri-Gondwana, South China, Kazakhstan terranes, Avalonia, and Baltica.

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The Late Ordovician (late Katian) Tcherskidium fauna consisted of large- and thick-shelled virgianid pentamerid brachiopods characterized by large and ribbed shells of Tcherskidium and Proconchidium and usually associated with Holorhynchus, Deloprosopus, and Eoconchidium. This unique fauna was widely distributed across several tectonic plates, largely confined to the paleoequatorial and especially the northern paleotropical zones, such as northern Laurentia, accretionary terranes of Alaska, Kolyma, Baltica, Siberia, Kazakh and adjacent terranes, and South China. In Laurentia, the eponymous genus Tcherskidium was predominant in regions north of the paleoequator and, in sharp contrast, was absent south of the paleoequator. In this study, Tcherskidium lonei n. sp. and Proconchidium schleyi n. sp. are described from Alaska and North Greenland, respectively, adding new data on the Tcherskidium fauna of the Late Ordovician Northern Hemisphere. Shell gigantism, together with the sharp paleobiogeographic division, suggests that the Late Ordovician (late Katian) Northern Hemisphere had a prevailing warm-water mass, probably due to the lack of large landmass beyond the northern tropics. This was in sharp contrast to the Southern Hemisphere, which was frequently influenced by cold-water invasions from the ice-bearing Gondwana supercontinent centered on the South Pole.

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A review of biodiversity curves of marine organisms indicates that, despite fluctuations in amplitude (some large), a large-scale, long-term radiation of life took place during the early Palaeozoic Era; it was aggregated by a succession of more discrete and regionalized radiations across geographies and within phylogenies. This major biodiversification within the marine biosphere started during late Precambrian time and was only finally interrupted in the Devonian Period. It includes both the Cambrian Explosion and the Great Ordovician Biodiversification Event. The establishment of modern marine ecosystems took place during a continuous chronology of the successive establishment of organisms and their ecological communities, developed during the ‘Cambrian substrate revolution’, the ‘Ordovician plankton revolution’, the ‘Ordovician substrate revolution’, the ‘Ordovician bioerosion revolution’ and the ‘Devonian nekton revolution’. At smaller scales, different regional but important radiations can be recognized geographically and some of them have been identified and named (e.g. those associated with the ‘Richmondian Invasion’ during Late Ordovician time in Laurentia and the contemporaneous ‘Boda event’ in parts of Europe and North Africa), in particular from areas that were in or moved towards lower latitudes, allowing high levels of speciation on epicontintental seas during these intervals. The datasets remain incomplete for many other geographical areas, but also for particular time intervals (e.g. during the late Cambrian ‘Furongian Gap’). The early Palaeozoic biodiversification therefore appears to be a long-term process, modulated by bursts in significant diversity and intervals of inadequate data, where its progressive character will become increasingly clearer with the availability of more complete datasets, with better global coverage and more advanced analytical techniques.

The brachiopods collected from the Kuanyinchiao Beds (Hirnantian, uppermost Ordovician) in Meitan and Zunyi counties, northern Guizhou, include 13 species and one undetermined taxon, dominated by Hirnantia sagittifera (M'Coy, 1851) (which accounts for over one-third of the specimens), together with common Eostropheodonta hirnantensis (M'Coy, 1851). They are assigned to the Hirnantia–Eostropheodonta Community, which probably inhabited a shallow-water, nearshore Benthic Assemblage (BA) 2 to upper BA 3 environment. Population analysis shows that the community was well adapted to this environment after the first phase of the end-Ordovician mass extinction. Representative specimens of all the species are illustrated, and a new species, Minutomena missa, is described herein. The variation in Hirnantia sagittifera was noted in many of previous studies but was not statistically evidenced. Here we have measured representative specimens of that famous species from the major paleoplates and terranes in the world, along with other species assigned to the genus from South China. Having used principal component analysis (PCA), significant variations in the species are documented statistically and revised, and three nominal species, one subspecies, and two morphotypes are now reassigned to Hirnantia sagittifera sensu stricto.

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This two-part special issue, Brachiopod Research into the Third Millennium, is published in honour of Sir Alwyn Williams (8 June 1921–4 April 2004). One section deals with fossil brachiopods while the other concentrates on aspects of modern material. The special issue comprises 23 invited papers, all dealing with current brachiopod research. In producing this special issue we honour the immense contribution made by the late Alwyn Williams to this field of research.