Systematic revision of the Late Ordovician brachiopod genera Eochonetes Reed, 1917 and Thaerodonta Wang, 1949 was conducted utilizing specimen-based morphometric and species-level phylogenetic analyses. Previous studies had recognized Thaerodonta and Eochonetes as either distinct taxonomic entities or synonyms. New multivariate and phylogenetic analyses confirm the synonymy of Thaerodonta with Eochonetes and provide a framework to assess evolutionary and ecological patterns within the clade. Multivariate analyses were employed to delineate species in morphospace and provided information on potential species relationships. Phylogenetic analysis was used to produce an evolutionary framework for taxonomic revision and identify character evolut...
<p>The phylogeographical evolution and the consequent changing distribution and diversity of rhyncho...
Independent molecular and morphological phylogenetic analyses have often produced discordant results...
The subclass Camerata (Crinoidea, Echinodermata) is a major group of Paleozoic crinoids that represe...
Systematic revision of the Late Ordovician brachiopod genera Eochonetes Reed, 1917 and Thaerodonta W...
<div><p>Species of the orthide brachiopod genus <i>Glyptorthis</i> occur as common constituents of L...
The order Strophomenida was an ecologically abundant and taxonomically diverse group of Palaeozoic b...
<p>Within the brachiopod Suborder Orthotetidina, only members of the Superfamily Chilidiopsoidea are...
The Late Ordovician mass extinction was an interval of high extinction with inferred low ecological ...
Hirnantian costate craniides are rare in the world and many have only been defined using open taxono...
The brachiopod order Atrypida originated in the Middle Ordovician and went extinct in the Late Devon...
Thirty-three species of strophomenid brachiopods, seven of them new, belonging to 23 genera are used...
Rhynchonellida is the stratigraphically oldest and phylogenetically most basal of the extant rhyncho...
<p>Supplementary Table 1. Vicariance and Geodispersal Matrices.</p> <p> </p> <p>Supplementary Figure...
The phylogeographical evolution and the consequent changing distribution and diversity of rhynchonel...
<p>The phylogeographical evolution and the consequent changing distribution and diversity of rhyncho...
Independent molecular and morphological phylogenetic analyses have often produced discordant results...
The subclass Camerata (Crinoidea, Echinodermata) is a major group of Paleozoic crinoids that represe...
Systematic revision of the Late Ordovician brachiopod genera Eochonetes Reed, 1917 and Thaerodonta W...
<div><p>Species of the orthide brachiopod genus <i>Glyptorthis</i> occur as common constituents of L...
The order Strophomenida was an ecologically abundant and taxonomically diverse group of Palaeozoic b...
<p>Within the brachiopod Suborder Orthotetidina, only members of the Superfamily Chilidiopsoidea are...
The Late Ordovician mass extinction was an interval of high extinction with inferred low ecological ...
Hirnantian costate craniides are rare in the world and many have only been defined using open taxono...
The brachiopod order Atrypida originated in the Middle Ordovician and went extinct in the Late Devon...
Thirty-three species of strophomenid brachiopods, seven of them new, belonging to 23 genera are used...
Rhynchonellida is the stratigraphically oldest and phylogenetically most basal of the extant rhyncho...
<p>Supplementary Table 1. Vicariance and Geodispersal Matrices.</p> <p> </p> <p>Supplementary Figure...
The phylogeographical evolution and the consequent changing distribution and diversity of rhynchonel...
<p>The phylogeographical evolution and the consequent changing distribution and diversity of rhyncho...
Independent molecular and morphological phylogenetic analyses have often produced discordant results...
The subclass Camerata (Crinoidea, Echinodermata) is a major group of Paleozoic crinoids that represe...