2016
DOI: 10.1080/02724634.2017.1245664
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Elegestolepisand its kin, the earliest monodontode chondrichthyans

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Cited by 16 publications
(15 citation statements)
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“…S13). These records suggest a global, mid-shelf center for sampling and diversity, and a null expectation of originations in deep subtidal and reef environments (more so than expected from previous studies focused on reef-bearing facies (15)). This is in stark contrast with shallower gnathostome ancestral habitats ( Fig.…”
mentioning
confidence: 49%
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“…S13). These records suggest a global, mid-shelf center for sampling and diversity, and a null expectation of originations in deep subtidal and reef environments (more so than expected from previous studies focused on reef-bearing facies (15)). This is in stark contrast with shallower gnathostome ancestral habitats ( Fig.…”
mentioning
confidence: 49%
“…Biogeographic patterns suggest that body-form divergence occurred in multiple shallow settings, increasing overall diversity. Micromeric forms occur alongside macromeric astraspids in the Ordovician of Laurentia, while robust galeaspids existed alongside gracile chondrichthyans in the early Silurian of Gondwana (4)(5)(6)(7)15,17,24,27,28).…”
Section: Endemicity In Coastal Waters May Have Later Promoted Originamentioning
confidence: 99%
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“…This 50-million-year record pre-dates the first appearance of teeth and articulated skeletons ( Leonodus and Celtiberina Botella, Donoghue & Martínez-Pérez , 2009 ; Doliodus Miller, Cloutier & Turner , 2003 ; Maisey, Miller & Turner , 2009 and Antarctilamna Young , 1982 ) of traditionally recognized chondrichthyans (euchondrichthyans sensu Pradel et al , 2014 ), as well as body fossils of acanthodian-grade stem chondrichthyans ( Brazeau & Friedman , 2015 and references therein). These, largely microscopic, remains include the elegestolepids ( Karatajūtė-Talimaa , 1973 ; Žigaitė & Karatajūtė-Talimaa , 2008 ; Andreev et al , in press ), sinacanthids ( Zhu , 1998 ; Sansom, Wang & Smith , 2005 ; Zeng , 1988 ), taxa such as Tezakia and Canyonlepis from the Ordovician of North America ( Sansom, Smith & Smith , 1996 ; Andreev et al , 2015 ), Tantalepis ( Sansom et al , 2012 ), Kannathalepis ( Märss & Gagnier , 2001 ) and Pilolepis ( Thorsteinsson , 1973 ), and, perhaps the most widely distributed and diverse collection of what Ørvig and Bendix-Almgreen, quoted in Karatajūtė-Talimaa ( 1995 ), referred to as ‘praechondrichthyes,’ the mongolepids ( Karatajūtė-Talimaa et al , 1990 ; Karatajūtė-Talimaa & Predtechenskyj , 1995 ; Sansom, Aldridge & Smith , 2000 ). It is the latter which this work concentrates on, re-assessing and re-defining previously described members of the Mongolepidida, and describing a new taxon that extends the range of the Order into the Ordovician, adding further evidence for a diversification of early chondrichthyans as part of the Great Ordovician Biodiversification Event that encompasses a wide variety of taxa, both invertebrate (e.g., Webby, Paris & Droser , ...…”
Section: Introductionmentioning
confidence: 99%
“…The taxa identified here are placed within the total-group Chondrichthyes and add to the burgeoning diversity of Lower Palaeozoic scales that are shark-like in their overall appearance, growth and histology. These include, in approximate stratigraphic order from the Darriwilian (Middle Ordovician) through to the Lower Devonian, Tantalepis [16], Tezakia and Canyonlepis [7,17], mongolepids [5,[18][19][20], elegestolepids [20,21] and Tuvalepis [22]. The relationship of these taxa to conventionally defined chondrichthyans (sensu [23]) remains contentious despite recent progress in integrating scale-based trees into the phylogenetic framework of early jawed gnathostomes [24].…”
Section: Introductionmentioning
confidence: 99%