That with the Genera Hemiganus, Ectoganus and Stylinodon It Forms
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SUPPLEMENTARY INFORMATION: Tables, Figures and References
Samuels, Regnault & Hutchinson, PeerJ Evolution of the patellar sesamoid bone in mammals SUPPLEMENTARY INFORMATION: Tables, Figures and References Supplementary Table S1: Mammaliaform patellar status$ Inclusive clades Genus and Stratigraphic age of Patellar Comments# (partial) species (and taxon, and location(s) state reference(s) used for 0/1/2 patellar status) (absent/ ‘patelloid’/ present) Sinoconodonta Sinoconodon Jurassic, China 0 Patellar groove absent, suggests no rigneyi (Kielan- patella Jaworowska et al., 2004) Sinoconodon is included on our phylogeny within tritylodontids. Morganucodonta Megazostrodon Late Triassic, southern 0 rudnerae (Jenkins Africa & Parrington, 1976) Morganucodonta Eozostrodon sp. Late Triassic, Wales 0 Asymmetric patellar groove, (Jenkins et al., specimens disarticulated so it is hard 1976) to assess the patella but appears absent Docodonta Castorocauda 164 Mya, mid-Jurassic, 0 Semi-aquatic adaptations lutrasimilis (Ji et China al., 2006) Docodonta Agilodocodon 164 Mya, mid-Jurassic, 0 scansorius (Meng China et al., 2015) Docodonta Docofossor 160 Mya, China 0 brachydactylus (Luo et al., 2015b) Docodonta Haldanodon 150-155 Mya, Late 0 Shallow patellar groove exspectatus Jurassic, Portugal (Martin, 2005b) Australosphenida Asfaltomylos Mid-Jurassic, South ? Postcranial material absent patagonicus America (Martin, 2005a) Australosphenida Ornithorhynchus Extant 2 Platypus, genome sequenced Monotremata anatinus (Warren, Hillier, Marshall Graves et (Herzmark, 1938; al., 2008) Rowe, 1988) Australosphenida Tachyglossus -
SUPPLEMENTARY INFORMATION: Tables, Figures and References
Samuels et al. Evolution of the patellar sesamoid bone in mammals SUPPLEMENTARY INFORMATION: Tables, Figures and References Supplementary Table S1: Mammals$ Higher taxa Genus sp. Estimated. age of Patellar Comments# (partial) specimen, location state 0/1/2 (absent/ ‘patelloid’/ present) Sinoconodonta Sinoconodon Jurassic 0 Patellar groove absent, suggests no rigneyi (Kielan- patella Jaworowska, Cifelli & Luo, Sinoconodon is included on our 2004) phylogeny within tritylodontids. Morganucodonta Megazostrodon Late Triassic, southern 0 rudnerae (Jenkins Africa & Parrington, 1976) Morganucodonta Eozostrodon sp. Late Triassic, Wales 0 Asymmetric patellar groove, (Jenkins et al., specimens disarticulated so it is hard 1976) to assess the patella but appears absent Docodonta Castorocauda 164 Mya, mid-Jurassic, 0 Semi-aquatic adaptations lutrasimilis (Ji, China Luo, Yuan et al., 2006) Docodonta Agilodocodon 164 Mya, mid-Jurassic, 0 scansorius China (Meng, Ji, Zhang et al., 2015) Docodonta Docofossor 160 Mya 0 brachydactylus (Luo, Meng, Ji et al., 2015) Docodonta Haldanodon 150-155 Mya, Late 0 Shallow patellar groove exspectatus Jurassic, Portugal (Martin, 2005b) Australosphenida Asfaltomylos Mid-Jurassic, South ? Postcranial material absent patagonicus America (Martin, 2005a) Australosphenida Ornithorhynchus Extant 2 Platypus, genome sequenced Monotremata anatinus (Warren, Hillier, Marshall Graves et (Herzmark, 1938; al., 2008) Rowe, 1988) Samuels et al. Australosphenida Tachyglossus + Extant 2 Echidnas Monotremata Zaglossus spp. (Herzmark, 1938; Rowe, 1988) Mammaliaformes Fruitafossor 150 Mya, Late Jurassic, 0 Phylogenetic status uncertain indet. windscheffeli (Luo Colorado & Wible, 2005) Mammaliaformes Volaticotherium Late Jurassic/Early ? Hindlimb material incomplete indet. antiquus (Meng, Cretaceous Hu, Wang et al., 2006) Eutriconodonta Jeholodens 120-125 Mya, Early 0 Poorly developed patellar groove jenkinsi (Ji, Luo Cretaceous, China & Ji, 1999) Eutriconodonta Gobiconodon spp. -
Some Sort. Whether the Particles Which Remove the Charge Come from The
some sort. Whether the particles which sloths. A second series, composed of Olzy- remove the charge come from the air, or chodectes and Conoryctes, is clearly an allied from the condensed gaseous layer, or from group, which probably gave origin to the the material of the body itself, is still in Armadillos. dispute. It appears to me that the mass These two series I have arranged under a of the evidence is in favor of the latter new suborder for which I have proposed hypothesis. But the possibility that the the name Ganodonta, and considered them phenomena may be complicated by elec- as constituting a primitive division of the trolytic conduction in the medium sur- Edentata. rounding the charged body,* must not be This suborder has been defined as fol- forgotten. lows : ('Primitive Edentates characterized ERNESTMERRITT. in the earlier forms by rooted teeth with CORNELLUNIVERSITY. divided fangs, having a more or less com- (To be conoluded.) plete enamel investment ;in the later forms by the teeth becoming hypsodont, rootless, of persistent growth, and by limitation of THE MRTH AXERICAAT ORIGIX OF THE EDENTAT3S.t tlie eaaniel covering to vertical bands in THE explorations of the American Mu- progressive decrease. By the presence of seum Paleontological party in the basin of incisors in both jaws, by a typical molar and the San Juan, New Mexico, during the past premolar dentition, by a trituberculate summer secured, among other important molar crown, which disappeared early in materials, the larger part of the anterior life through wear, leaving the dentine ex- limb of Wittacotherizun multi,fragunz Cope, as- posed." sociated with the lower jaws and a number The evidence of the Edentato affinities of tlie upper teeth. -
Diversity of Hypsodont Teeth in Mammalian Dentitions – Construction and Classification
Palaeontographica, Abt. A: Palaeozoology – Stratigraphy Article Vol. 294, Issues 1–3: 63–94 Stuttgart, July 2011 Diversity of hypsodont teeth in mammalian dentitions – construction and classification by Wighart v. Koenigswald with 9 text-figures and 3 tables This paper is dedicated with great respect to Prof. em. Dr. Adolf Seilacher of Tübingen and Yale. Dolf successfully inspired many students with his understanding of ‘Constructional Morphology.’ He opened many eyes, mine included, to the trade-offs of history, function, and construction that constrain morphology. Zusammenfassung Hypsodontie, so wie der Begriff hier gebraucht wird, beschreibt Zähne, deren Krone parallel zur Wa chstumsrichtung verlängert ist. Diese Zahnform kann in allen Zahnpositionen auftreten. Die Hypodontie wird als die heterochrone Verlängerung bestimmter ontogenetischer Phasen während der Zahnbildung auf Kosten der anderen Phasen interpretiert. Mit drei Kriterien lässt sich die Viel- falt hypsodonter Zähne unterscheiden: zum einen geht es darum, welche Phase (oder Phasen) in der Ontogenie verlängert sind, zum anderen um den Grad der Hypsodontie (zunehmende Kronenhöhe bis zur Euhypsodontie) und drittens um die Art der Abkauung (ein ausbalancierter Abrieb, bei dem Nachwachsen und Abrieb im Gleichgewicht stehen, oder ein freies Größenwachstum). Die Un- terteilung der Ontogenie in vier Phasen (I =Zahnspitzen; II =Seitenwände, III =Dentinoberfläche (Zahnhals) und IV =differen- zierte Wurzeln) ist zwar künstlich, ermöglicht aber, die Diversität hypsodonter Zähne in sechs Kategorien zu gliedern. 1. Vielspitzen- Hypsodontie (verlängerte Phase I); 2. Spitzen-Hypsodontie (verschmolzene Phasen I und II); 3. Seitenwand-Hypsodontie (verlänger- te Phase II); 4. Schmelzband-Hypsodontie (Phasen II und III bilden den Zahn gleichzeitig); 5. Partielle Hypsodontie (Phasen II, III und IV sind gleichzeitig aktiv) und 6. -
(Mammalia: Eutheria) from the San Juan Basin of New Mexico and Comments on the Phylogeny and Functional Morphology of 'Archaic' Mammals
Edinburgh Research Explorer New Specimens of the Rare Taeniodont Wortmania (Mammalia: Eutheria) from the San Juan Basin of New Mexico and Comments on the Phylogeny and Functional Morphology of 'Archaic' Mammals Citation for published version: Williamson, TE, Brusatte, SL & Viriot, L (ed.) 2013, 'New Specimens of the Rare Taeniodont Wortmania (Mammalia: Eutheria) from the San Juan Basin of New Mexico and Comments on the Phylogeny and Functional Morphology of 'Archaic' Mammals', PLoS ONE, vol. 8, no. 9, E75886. https://doi.org/10.1371/journal.pone.0075886 Digital Object Identifier (DOI): 10.1371/journal.pone.0075886 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: PLoS ONE Publisher Rights Statement: This is an Open-Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly cited. General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact [email protected] providing details, and we will remove access to the work immediately and investigate your claim. Download date: 09. -
Extant Taxa Stem Frogs Stem Turtles Stem Lepidosaurs Stem Squamates
Stem Taxa - Peters 2016 851 taxa, 228 characters 100 Eldeceeon 1990.7.1 91 Eldeceeon holotype 100 Romeriscus Ichthyostega Gephyrostegus watsoni Pederpes 85 Eryops 67 Solenodonsaurus 87 Proterogyrinus 100 Chroniosaurus Eoherpeton 94 72 Chroniosaurus PIN3585/124 98 Seymouria Chroniosuchus Kotlassia Stem 58 94 Westlothiana Utegenia Casineria 84 81 Amphibamus Brouffia 95 72 Cacops 93 77 Coelostegus Paleothyris 98 Doleserpeton 84 91 78 100 Gerobatrachus Hylonomus Rana Archosauromorphs Protorothyris MCZ1532 95 66 98 Adelospondylus 85 Protorothyris CM 8617 89 Brachydectes Protorothyris MCZ 2149 Eocaecilia 87 86 Microbrachis Vaughnictis Pantylus 80 89 75 94 Anthracodromeus Elliotsmithia 90 Utaherpeton 51 Apsisaurus Kirktonecta 95 90 86 Aerosaurus 96 Tuditanus 67 90 Varanops Stem Frogs 59 94 Eoserpeton Varanodon Diplocaulus Varanosaurus FMNH PR 1760 100 Sauropleura 62 84 Varanosaurus BSPHM 1901 XV20 88 Ptyonius 89 Archaeothyris 70 Scincosaurus Euryodus primus Ophiacodon 74 82 84 Micraroter Haptodus 91 Rhynchonkos 97 82 Secodontosaurus Batropetes 85 76 100 Dimetrodon 97 Sphenacodon Silvanerpeton Ianthodon 85 Edaphosaurus Gephyrostegeus bohemicus 99 Stem100 Reptiles 80 82 Ianthasaurus Glaucosaurus 94 Cutleria 100 Urumqia Bruktererpeton Stenocybus Stem Mammals 63 97 Thuringothyris MNG 7729 62 IVPP V18117 82 Thuringothyris MNG 10183 87 62 71 Kenyasaurus 82 Galechirus 52 Suminia Saurorictus Venjukovia 99 99 97 83 70 Cephalerpeton Opisthodontosaurus 94 Eodicynodon 80 98 Reiszorhinus 100 Dicynodon 75 Concordia KUVP 8702a Hipposaurus 100 98 96 Concordia -
Mammalian Distal Humerus Fossils from Eastern Montana, USA with Implications for the Cretaceous-Paleogene Mass Extinction and the Adaptive Radiation of Placentals
Palaeontologia Electronica palaeo-electronica.org Mammalian distal humerus fossils from eastern Montana, USA with implications for the Cretaceous-Paleogene mass extinction and the adaptive radiation of placentals Lauren B. DeBey and Gregory P. Wilson ABSTRACT Postcrania of Cretaceous-Paleogene (K-Pg) mammals offer insights into richness, body size, and locomotor ecology that supplement patterns from well-sampled dental assemblages. Here, we describe and morphotype 50 distal humeri from Lancian–Puer- can assemblages of eastern Montana. Using geometric morphometric analysis of a taxonomically broad sample of humeri from extant small-bodied therians of diverse locomotor modes, we constrain locomotor inferences of some morphotypes. We use this database to preliminarily assess body-size and locomotor diversity across the K- Pg boundary. The seven Lancian humerus morphotypes include the multituberculates ?Mesodma sp., ?Cimolodon nitidus, and ?Meniscoessus robustus and the metatherian ?Didelphodon vorax. Morphotype richness decreased to four or five across the K-Pg boundary and rebounded in the late Puercan to six, mostly eutherian, morphotypes. Puercan morphotypes include the multituberculate ?Stygimys kuszmauli, the “plesi- adapiform” primate ?Purgatorius, small and large archaic ungulates, a possible palaeo- ryctid, and a very large eutherian. Humerus size data imply a decrease in body size across the K-Pg boundary, followed by an increase by the late Puercan, a trend consis- tent with the dental fossil record. Geometric morphometrics analysis and functional morphology imply greater locomotor diversity among K-Pg mammals than previously recognized: we infer that most Lancian and Puercan multituberculates were arboreal; the Lancian eutherian was arboreal or semifossorial; the early Puercan palaeoryctid was semifossorial and the small archaic ungulate was terrestrial; and the late Puercan “plesiadapiform” primate was arboreal and the large archaic ungulate was scansorial. -
The Postcranial Morphology and Phylogeny of Taeniodonts (Mammalia: Taeniodonta); Determining Locomotor Adaptations in Paleogene
THE POSTCRANIAL MORPHOLOGY AND PHYLOGENY OF TAENIODONTS (MAMMALIA: TAENIODONTA); DETERMINING LOCOMOTOR ADAPTATIONS IN PALEOGENE MAMMALS KYNIGOPOULOU, Zoi, University of Edinburgh, Edinburgh, United Kingdom; SHELLEY, Sarah L., Carnegie Museum of Natural History, Pittsburgh, PA, United States of America; WILLIAMSON, Thomas E., New Mexico Museum of Natural History, Albuquerque, NM, United States of America; BRUSATTE, Stephen L., University of Edinburgh, Edinburgh, United Kingdom After the Cretaceous-Paleogene (K-Pg) mass extinction mammals, which originated during the Mesozoic, managed to survive and thrive. However, the tempo and mode of evolution for eutherians (placentals and close relatives) after the extinction are still unclear. An ideal group to investigate the post KPg evolution of mammals is the taeniodonts, as they are among the few taxa to purportedly cross the boundary. They then underwent a radiation in the early Paleogene and are defined primarily by their unusual dentition which is suited to chew an abrasive and tough diet. Ten genera of taeniodonts are currently recognized and are commonly arranged into two families. The Conoryctidae is usually considered to have a more generalized body plan while Stylinodontidae possess relatively extreme digging adaptations and more highly derived dentitions with enlarged canines. We conducted a phylogenetic analysis by applying parsimony and Bayesian techniques to a dataset of characters gathered from extensive observation of new specimens. We found limited support for the conoryctid-stylinodontid division and the genera Conoryctes and Onychodectes are placed as key basal taxa outside the clade of the more robust derived taxa (Wortmania, Ectoganus, Psittacotherium, Stylinodon). We then assessed postcranial bones to determine functional modes for taeniodonts and to test changes across phylogeny. -
Stratigraphy of the Washakie Basin, Wyoming
Stratigraphy of the Washakie Formation in the Washakie Basin, Wyoming GEOLOGICAL SURVEY BULLETIN 1369 Stratigrap?y of the Washakie_. Form.ation· -in the W qshakie · Basin, Wyoming By HENRY W. ROEHLER GEOLOGICAL. SURVEY BULLETIN 1 3 6 9 The name Washakie F?rmation is revived for Eocene fluvial . rocks that overlie the Green River Formation in the Washakie Basin. The formation is then divided into the· Kinney Rim and Adobe Town Members UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON 1973 UNITED STATES DEPARTMENT OF THE INTERIOR ROGERS C. B. MORTON, Secretary GEOLOGICAL SURVEY V. E. McKelvey, Director Library of Congress catalog-card No. 72-600329 For sale by the Superintendent of Documents, U. S. Government Printing Office t Washington, D. C. 20402 Stock No. 2401-00286 CONTENTS Page Abstract ------------------------------------------------------- 1 Int~~-9-tion ---:-----.---:------------------------------'--------- 1 ·!F>.'q:rpose of mvestigatiOns __ ----__ --____ --_ --____ ----_______ _ 1 Acknowledgments ----------------------------------------- 2 Location and geologic setting of the Washakie Basin ---------- 2 Nomenclature and history of geological and paleontological in- vestigations __________ --__ -------------------------------- 3 Gompa'risons of the Washakie, Bridger, and Uinta Formations _ 8 Washakie Formation __________________________________________ _ 12 Kinney Rim Member -------------------------------------- 12 Adobe Town Member --------------------------------------- 14 Outcrops -------------------------------------------------- -
Reptile Family Tree
Thelodus 78 Rhincodon Manta 99 Squatina 70 Aetobatus 79 Cladoselache 59 Chlamydoselachus 92 Isurus 88 Sphyrna 95 Rhinobatos 70 Heterodontus 90 Belantsea Chimaera 73 97 Iniopteryx Falcatus 85 99 Chondrosteus Pseudoscaphirhynchus 82 Amia Hybodus 60 52 Gregorius 99 90 Entelognathus 84 Hoplosternum 95 Clarias 74 Ictalurus 98 Coccosteus 100 96 Mcnamaraspis Dunkleosteus 73 100 100 Romundina Dapedium 92 Bothriolepis 81 Cheirodus 83 Dicksonosteus <50 Lepidotes 100 Qilinyu 100 Robustichthys Menaspis 88 Lepisosteus Semionotus Reptile Family Tree - Peters 2019 1594+ taxa, 235 characters 58 Perleidus 98 Brachyacanthus <50 Notopterus Ischnacanthus 54 Osteoglossum 85 100 Mimipiscis Pholidophorus * red taxa have too few traits to include on this list, but were tested with small subsets Moythomasia 100 Pteronisculus 69 Coccocephalichthys 95 Cheirolepis <50 Saurichthys 68 74 100 Malacosteus 69 Thoracopterus Chauliodus 58 Engraulis 80 100 Lepidogalaxias 99 Trachinocephalus Megalops Chiasmodon <58 95 Thunnus 77 Strunius Polydactylus Onychodus 79 Heteronectes 67 95 51 80 Barameda 79 Psettodes 100 Gymnothorax Hippoglossus Eurypharynx 74 <50 Anarhichas 94 Allenypterus Xiphactinus 88 92 Quebecius 54 Coryphaena 88 Holoptychius Remora 98 Miguashia 98 Latimeria 59 Sphyraena Esox 94 84 Stensioella 81 Kenichthys 81 Serrasalmus 84 Youngolepis 94 Perca 98 Cyprinus 79 Guiyu 76 Psarolepis <50 <50 Prionotus 90 Powichthys <50 Dactylopterus 83 Polypterus 94 100 Erpetoichthys Aphanopus 68 85 Uranolophus 99 Exocoetus Dipnorhynchus Archosauromorpha 89 68 Tylosurus Howidipterus -
Reptile Family Tree Peters 2021 1909 Taxa, 235 Characters
Turinia Enoplus Chondrichtyes Jagorina Gemuendina Manta Chordata Loganellia Ginglymostoma Rhincodon Branchiostoma Tristychius Pikaia Tetronarce = Torpedo Palaeospondylus Craniata Aquilolamna Tamiobatis Myxine Sphyrna Metaspriggina Squalus Arandaspis Pristis Poraspis Rhinobatos Drepanaspis Cladoselache Pteromyzon adult Promissum Chlamydoselachus Pteromyzon hatchling Aetobatus Jamoytius Squatina Birkenia Heterodontus Euphanerops Iniopteryx Drepanolepis Helodus Callorhinchus Haikouichthys Scaporhynchus Belantsea Squaloraja Hemicyclaspis Chimaera Dunyu CMNH 9280 Mitsukurina Rhinochimaera Tanyrhinichthys Isurus Debeerius Thelodus GLAHM–V8304 Polyodon hatchling Cetorhinus Acipenser Yanosteus Oxynotus Bandringa PF8442 Pseudoscaphirhynchus Isistius Polyodon adult Daliatus Bandringa PF5686 Gnathostomata Megachasma Xenacanthus Dracopristis Akmonistion Ferromirum Strongylosteus Ozarcus Falcatus Reptile Family Tree Chondrosteus Hybodus fraasi Hybodus basanus Pucapampella Osteichthyes Orodus Peters 2021 1943 taxa, 235 characters Gregorius Harpagofututor Leptolepis Edestus Prohalecites Gymnothorax funebris Doliodus Gymnothorax afer Malacosteus Eurypharynx Amblyopsis Lepidogalaxias Typhlichthys Anableps Kryptoglanis Phractolaemus Homalacanthus Acanthodes Electrophorus Cromeria Triazeugacanthus Gymnotus Gorgasia Pholidophorus Calamopleurus Chauliodus Bonnerichthys Dactylopterus Chiasmodon Osteoglossum Sauropsis Synodus Ohmdenia Amia Trachinocephalus BRSLI M1332 Watsonulus Anoplogaster Pachycormus Parasemionotus Aenigmachanna Protosphyraena Channa Aspidorhynchus -
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DENVER MUSEUM OF NATURE & SCIENCE ANNALS NUMBER 1, SEPTEMBER 1, 2009 Land Mammal Faunas of North America Rise and Fall During the Early Eocene Climatic Optimum Michael O. Woodburne, Gregg F. Gunnell, and Richard K. Stucky WWW.DMNS.ORG/MAIN/EN/GENERAL/SCIENCE/PUBLICATIONS The Denver Museum of Nature & Science Annals is an Frank Krell, PhD, Editor-in-Chief open-access, peer-reviewed scientific journal publishing original papers in the fields of anthropology, geology, EDITORIAL BOARD: paleontology, botany, zoology, space and planetary Kenneth Carpenter, PhD (subject editor, Paleontology and sciences, and health sciences. Papers are either authored Geology) by DMNS staff, associates, or volunteers, deal with DMNS Bridget Coughlin, PhD (subject editor, Health Sciences) specimens or holdings, or have a regional focus on the John Demboski, PhD (subject editor, Vertebrate Zoology) Rocky Mountains/Great Plains ecoregions. David Grinspoon, PhD (subject editor, Space Sciences) Frank Krell, PhD (subject editor, Invertebrate Zoology) The journal is available online at www.dmns.org/main/en/ Steve Nash, PhD (subject editor, Anthropology and General/Science/Publications free of charge. Paper copies Archaeology) are exchanged via the DMNS Library exchange program ([email protected]) or are available for purchase EDITORIAL AND PRODUCTION: from our print-on-demand publisher Lulu (www.lulu.com). Betsy R. Armstrong: project manager, production editor DMNS owns the copyright of the works published in the Ann W. Douden: design and production Annals, which are published under the Creative Commons Faith Marcovecchio: proofreader Attribution Non-Commercial license. For commercial use of published material contact Kris Haglund, Alfred M. Bailey Library & Archives ([email protected]).