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Bivalves from the Changhsingian (upper Permian) Bellerophon Formation of the Dolomites (Italy): ancestors of Lower Triassic post‐extinction benthic communities.
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- Papers in Palaentology, 2023, v. 9, n. 2, p. 1, doi. 10.1002/spp2.1486
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An expanded Smithian–Spathian (Lower Triassic) boundary from a reefal build‐up record in Oman: implications for conodont taxonomy, high‐resolution biochronology and the carbon isotope record.
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- Papers in Palaentology, 2023, v. 9, n. 1, p. 1, doi. 10.1002/spp2.1481
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Gastropods underwent a major taxonomic turnover during the end-Triassic marine mass extinction event.
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- PLoS ONE, 2022, v. 17, n. 11, p. 1, doi. 10.1371/journal.pone.0276329
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Gradual warming prior to the end‐Permian mass extinction.
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- Palaeontology, 2022, v. 65, n. 5, p. 1, doi. 10.1111/pala.12621
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Fluorescent colour patterns in the basal pectinid Pleuronectites from the Middle Triassic of Central Europe: origin, fate and taxonomic implications of fluorescence.
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- Palaeontology, 2022, v. 65, n. 5, p. 1, doi. 10.1111/pala.12625
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The Anisian (Middle Triassic) brachiopods from the southern Qilian Mountains, north‐western China.
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- Papers in Palaentology, 2022, v. 8, n. 5, p. 1, doi. 10.1002/spp2.1468
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Boreognathus pogorevichi, a remarkable new polychaete annelid from the lower Permian of the Pechora Basin, Russia.
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- Papers in Palaentology, 2022, v. 8, n. 5, p. 1, doi. 10.1002/spp2.1461
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Phosphatized adductor muscle remains in a Cenomanian limid bivalve from Villers-sur-Mer (France)
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- Swiss Journal of Paleontology, 2022, v. 141, n. 1, p. 1, doi. 10.1186/s13358-022-00252-4
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Is the relative thickness of ammonoid septa influenced by ocean acidification, phylogenetic relationships and palaeogeographic position?
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- Swiss Journal of Paleontology, 2022, v. 141, n. 1, p. 1, doi. 10.1186/s13358-022-00246-2
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Morphological–phylogenetic analysis of the late Cenozoic Chlamydini von Teppner (Bivalvia, Pectinidae) of southern South America.
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- Papers in Palaentology, 2021, v. 7, n. 4, p. 1825, doi. 10.1002/spp2.1365
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The main stage of recovery after the end-Permian mass extinction: taxonomic rediversification and ecologic reorganization of marine level-bottom communities during the Middle Triassic.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.11654
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Upper Toarcian (Lower Jurassic) marine gastropods from the Cleveland Basin, England: systematics, palaeobiogeography and contribution to biotic recovery from the early Toarcian extinction event.
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- Papers in Palaentology, 2021, v. 7, n. 2, p. 885, doi. 10.1002/spp2.1322
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Taxonomic identification using virtual palaeontology and geometric morphometrics: a case study of Jurassic nerineoidean gastropods.
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- Palaeontology, 2021, v. 64, n. 2, p. 249, doi. 10.1111/pala.12521
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Gastropods from the Jurassic neptunian sills of Rocca Busambra (north‐western Sicily, Italy): Patellogastropoda, Pleurotomarioidea, Scissurelloidea, Fissurelloidea and Eucycloidea.
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- Papers in Palaentology, 2021, v. 7, n. 1, p. 27, doi. 10.1002/spp2.1258
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A Changhsingian (late Permian) nautiloid assemblage from Gujiao, South China.
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- Papers in Palaentology, 2021, v. 7, n. 1, p. 329, doi. 10.1002/spp2.1275
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A highly diverse bivalve fauna from a Bithynian (Anisian, Middle Triassic) Tubiphytes‐microbial buildup in North Dobrogea (Romania).
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- Papers in Palaentology, 2021, v. 7, n. 1, p. 447, doi. 10.1002/spp2.1286
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The Serbian Lake System: a stepping stone for freshwater molluscs in the middle Miocene.
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- Papers in Palaentology, 2020, v. 6, n. 4, p. 533, doi. 10.1002/spp2.1308
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Is Cyclocardia (Conrad) a wastebasket taxon? Exploring the phylogeny of the most diverse genus of the Carditidae (Archiheterodonta, Bivalvia).
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- Palaeontology, 2020, v. 63, n. 3, p. 477, doi. 10.1111/pala.12467
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What is macroevolution?
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- Palaeontology, 2020, v. 63, n. 1, p. 1, doi. 10.1111/pala.12465
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Fossil liberation: a model to explain high biodiversity in the Triassic Cassian Formation.
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- Palaeontology, 2020, v. 63, n. 1, p. 85, doi. 10.1111/pala.12441
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Early Triassic benthic invertebrates from the Great Bank of Guizhou, South China: systematic palaeontology and palaeobiology.
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- Papers in Palaentology, 2019, v. 5, n. 4, p. 613, doi. 10.1002/spp2.1252
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Body size changes in bivalves of the family Limidae in the aftermath of the end‐Triassic mass extinction: the Brobdingnag effect.
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- Palaeontology, 2019, v. 62, n. 4, p. 561, doi. 10.1111/pala.12415
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New high‐resolution age data from the Ediacaran–Cambrian boundary indicate rapid, ecologically driven onset of the Cambrian explosion.
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- Terra Nova, 2019, v. 31, n. 1, p. 49, doi. 10.1111/ter.12368
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A highly diverse early Middle Triassic bivalve fauna from North Dobrogea (Romania) and its implication for bivalve recovery after the end-Permian mass extinction.
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- Geophysical Research Abstracts, 2019, v. 21, p. 1
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An Early Triassic (Dienerian) microgastropod assemblage from the Salt Range, Pakistan and its implication for gastropod recovery from the end-Permian mass extinction.
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- Bulletin of Geosciences, 2018, v. 93, n. 1, p. 56, doi. 10.3140/bull.geosci.1682
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Endo- and epilithic faunal succession in a Pliocene-Pleistocene cave on Rhodes, Greece: record of a transgression.
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- Palaeontology, 2017, v. 60, n. 5, p. 663, doi. 10.1111/pala.12312
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Geologically oldest oysters were epizoans on Early Triassic ammonoids.
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- Journal of Molluscan Studies, 2017, v. 83, n. 3, p. 253, doi. 10.1093/mollus/eyx018
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Biostratigraphy and geometric morphometrics of conchostracans (Crustacea, Branchiopoda) from the Late Triassic fissure deposits of Cromhall Quarry, UK.
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- Palaeontology, 2017, v. 60, n. 3, p. 349, doi. 10.1111/pala.12288
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Revision of the genus Anasibirites Mojsisovics (Ammonoidea): an iconic and cosmopolitan taxon of the late Smithian (Early Triassic) extinction.
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- Papers in Palaentology, 2016, v. 2, n. 1, p. 155, doi. 10.1002/spp2.1036
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A NEW PHOSPHATIC-SHELLED CIRRIPEDE (CRUSTACEA, THORACICA) FROM THE LOWER JURASSIC (TOARCIAN) OF GERMANY - THE OLDEST EPIPLANKTONIC BARNACLE.
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- Palaeontology, 2016, v. 59, n. 1, p. 59, doi. 10.1111/pala.12207
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Competition in slow motion: the unusual case of benthic marine communities in the wake of the end- Permian mass extinction.
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- Palaeontology, 2015, v. 58, n. 5, p. 871, doi. 10.1111/pala.12186
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Conodonts from the Early Triassic microbialite of Guangxi ( South China): implications for the definition of the base of the Triassic System.
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- Palaeontology, 2015, v. 58, n. 3, p. 563, doi. 10.1111/pala.12162
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Recovery of benthic marine communities from the end- Permian mass extinction at the low latitudes of eastern Panthalassa.
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- Palaeontology, 2014, v. 57, n. 3, p. 547, doi. 10.1111/pala.12076
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Palaeoecology of the Spathian Virgin Formation (Utah, USA) and its implications for the Early Triassic recovery.
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- Acta Palaeontologica Polonica, 2013, v. 58, n. 1, p. 149, doi. 10.4202/app.2011.0060
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Olenekian (Early Triassic) bivalves from the Salt Range and Surghar Range, Pakistan.
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- Palaeontology, 2012, v. 55, n. 5, p. 1043, doi. 10.1111/j.1475-4983.2012.01176.x
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Dienerian (Early Triassic) ammonoids from the Candelaria Hills (Nevada, USA) and their significance for palaeobiogeography and palaeoceanography.
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- Swiss Journal of Geosciences, 2011, v. 104, n. 1, p. 161, doi. 10.1007/s00015-011-0055-3
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FIRST RECORD OF A HETERODONT BIVALVE (MOLLUSCA) FROM THE EARLY TRIASSIC: PALAEOECOLOGICAL SIGNIFICANCE AND IMPLICATIONS FOR THE ‘LAZARUS PROBLEM’.
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- Palaeontology, 2005, v. 48, n. 6, p. 1131, doi. 10.1111/j.1475-4983.2005.00505.x
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Taxonomy and phylogeny of cementing Triassic bivalves (families Prospondylidae, Plicatulidae, Dimyidae and Ostreidae).
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- Palaeontology, 2001, v. 44, n. 2, p. 339, doi. 10.1111/1475-4983.00183
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