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Reptile Family Tree
Reptile Family Tree - Peters 2015 Distribution of Scales, Scutes, Hair and Feathers Fish scales 100 Ichthyostega Eldeceeon 1990.7.1 Pederpes 91 Eldeceeon holotype Gephyrostegus watsoni Eryops 67 Solenodonsaurus 87 Proterogyrinus 85 100 Chroniosaurus Eoherpeton 94 72 Chroniosaurus PIN3585/124 98 Seymouria Chroniosuchus Kotlassia 58 94 Westlothiana Casineria Utegenia 84 Brouffia 95 78 Amphibamus 71 93 77 Coelostegus Cacops Paleothyris Adelospondylus 91 78 82 99 Hylonomus 100 Brachydectes Protorothyris MCZ1532 Eocaecilia 95 91 Protorothyris CM 8617 77 95 Doleserpeton 98 Gerobatrachus Protorothyris MCZ 2149 Rana 86 52 Microbrachis 92 Elliotsmithia Pantylus 93 Apsisaurus 83 92 Anthracodromeus 84 85 Aerosaurus 95 85 Utaherpeton 82 Varanodon 95 Tuditanus 91 98 61 90 Eoserpeton Varanops Diplocaulus Varanosaurus FMNH PR 1760 88 100 Sauropleura Varanosaurus BSPHM 1901 XV20 78 Ptyonius 98 89 Archaeothyris Scincosaurus 77 84 Ophiacodon 95 Micraroter 79 98 Batropetes Rhynchonkos Cutleria 59 Nikkasaurus 95 54 Biarmosuchus Silvanerpeton 72 Titanophoneus Gephyrostegeus bohemicus 96 Procynosuchus 68 100 Megazostrodon Mammal 88 Homo sapiens 100 66 Stenocybus hair 91 94 IVPP V18117 69 Galechirus 69 97 62 Suminia Niaftasuchus 65 Microurania 98 Urumqia 91 Bruktererpeton 65 IVPP V 18120 85 Venjukovia 98 100 Thuringothyris MNG 7729 Thuringothyris MNG 10183 100 Eodicynodon Dicynodon 91 Cephalerpeton 54 Reiszorhinus Haptodus 62 Concordia KUVP 8702a 95 59 Ianthasaurus 87 87 Concordia KUVP 96/95 85 Edaphosaurus Romeria primus 87 Glaucosaurus Romeria texana Secodontosaurus -
Live Birth in an Archosauromorph Reptile
ARTICLE Received 8 Sep 2016 | Accepted 30 Dec 2016 | Published 14 Feb 2017 DOI: 10.1038/ncomms14445 OPEN Live birth in an archosauromorph reptile Jun Liu1,2,3, Chris L. Organ4, Michael J. Benton5, Matthew C. Brandley6 & Jonathan C. Aitchison7 Live birth has evolved many times independently in vertebrates, such as mammals and diverse groups of lizards and snakes. However, live birth is unknown in the major clade Archosauromorpha, a group that first evolved some 260 million years ago and is represented today by birds and crocodilians. Here we report the discovery of a pregnant long-necked marine reptile (Dinocephalosaurus) from the Middle Triassic (B245 million years ago) of southwest China showing live birth in archosauromorphs. Our discovery pushes back evidence of reproductive biology in the clade by roughly 50 million years, and shows that there is no fundamental reason that archosauromorphs could not achieve live birth. Our phylogenetic models indicate that Dinocephalosaurus determined the sex of their offspring by sex chromosomes rather than by environmental temperature like crocodilians. Our results provide crucial evidence for genotypic sex determination facilitating land-water transitions in amniotes. 1 School of Resources and Environmental Engineering, Hefei University of Technology, Hefei 230009, China. 2 Chengdu Center, China Geological Survey, Chengdu 610081, China. 3 State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, CAS, Nanjing 210008, China. 4 Department of Earth Sciences, Montana State University, Bozeman, Montana 59717, USA. 5 School of Earth Sciences, University of Bristol, Bristol BS8 1RJ, UK. 6 School of Life and Environmental Sciences, The University of Sydney, Sydney, New South Wales 2006, Australia. -
Physical and Environmental Drivers of Paleozoic Tetrapod Dispersal Across Pangaea
ARTICLE https://doi.org/10.1038/s41467-018-07623-x OPEN Physical and environmental drivers of Paleozoic tetrapod dispersal across Pangaea Neil Brocklehurst1,2, Emma M. Dunne3, Daniel D. Cashmore3 &Jӧrg Frӧbisch2,4 The Carboniferous and Permian were crucial intervals in the establishment of terrestrial ecosystems, which occurred alongside substantial environmental and climate changes throughout the globe, as well as the final assembly of the supercontinent of Pangaea. The fl 1234567890():,; in uence of these changes on tetrapod biogeography is highly contentious, with some authors suggesting a cosmopolitan fauna resulting from a lack of barriers, and some iden- tifying provincialism. Here we carry out a detailed historical biogeographic analysis of late Paleozoic tetrapods to study the patterns of dispersal and vicariance. A likelihood-based approach to infer ancestral areas is combined with stochastic mapping to assess rates of vicariance and dispersal. Both the late Carboniferous and the end-Guadalupian are char- acterised by a decrease in dispersal and a vicariance peak in amniotes and amphibians. The first of these shifts is attributed to orogenic activity, the second to increasing climate heterogeneity. 1 Department of Earth Sciences, University of Oxford, South Parks Road, Oxford OX1 3AN, UK. 2 Museum für Naturkunde, Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Invalidenstraße 43, 10115 Berlin, Germany. 3 School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham B15 2TT, UK. 4 Institut -
Exceptional Vertebrate Biotas from the Triassic of China, and the Expansion of Marine Ecosystems After the Permo-Triassic Mass Extinction
Earth-Science Reviews 125 (2013) 199–243 Contents lists available at ScienceDirect Earth-Science Reviews journal homepage: www.elsevier.com/locate/earscirev Exceptional vertebrate biotas from the Triassic of China, and the expansion of marine ecosystems after the Permo-Triassic mass extinction Michael J. Benton a,⁎, Qiyue Zhang b, Shixue Hu b, Zhong-Qiang Chen c, Wen Wen b, Jun Liu b, Jinyuan Huang b, Changyong Zhou b, Tao Xie b, Jinnan Tong c, Brian Choo d a School of Earth Sciences, University of Bristol, Bristol BS8 1RJ, UK b Chengdu Center of China Geological Survey, Chengdu 610081, China c State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences (Wuhan), Wuhan 430074, China d Key Laboratory of Evolutionary Systematics of Vertebrates, Institute of Vertebrate Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China article info abstract Article history: The Triassic was a time of turmoil, as life recovered from the most devastating of all mass extinctions, the Received 11 February 2013 Permo-Triassic event 252 million years ago. The Triassic marine rock succession of southwest China provides Accepted 31 May 2013 unique documentation of the recovery of marine life through a series of well dated, exceptionally preserved Available online 20 June 2013 fossil assemblages in the Daye, Guanling, Zhuganpo, and Xiaowa formations. New work shows the richness of the faunas of fishes and reptiles, and that recovery of vertebrate faunas was delayed by harsh environmental Keywords: conditions and then occurred rapidly in the Anisian. The key faunas of fishes and reptiles come from a limited Triassic Recovery area in eastern Yunnan and western Guizhou provinces, and these may be dated relative to shared strati- Reptile graphic units, and their palaeoenvironments reconstructed. -
Elachistosuchus Huenei Janensch, 1949 (Reptilia: Diapsida) from the Upper Triassic of Germany and Its Relevance for the Origin of Sauria
RESEARCH ARTICLE Anatomy of the Enigmatic Reptile Elachistosuchus huenei Janensch, 1949 (Reptilia: Diapsida) from the Upper Triassic of Germany and Its Relevance for the Origin of Sauria Gabriela Sobral1☯*, Hans-Dieter Sues2☯, Johannes Müller1☯ 1 Museum für Naturkunde Berlin, Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Berlin, Germany, 2 Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, MRC 121, Washington, DC, United States of America ☯ These authors contributed equally to this work. * [email protected] OPEN ACCESS Citation: Sobral G, Sues H-D, Müller J (2015) Abstract Anatomy of the Enigmatic Reptile Elachistosuchus huenei Janensch, 1949 (Reptilia: Diapsida) from the The holotype and only known specimen of the enigmatic small reptile Elachistosuchus hue- Upper Triassic of Germany and Its Relevance for the nei Janensch, 1949 from the Upper Triassic (Norian) Arnstadt Formation of Saxony-Anhalt Origin of Sauria. PLoS ONE 10(9): e0135114. μ doi:10.1371/journal.pone.0135114 (Germany) is redescribed using CT scans of the material. This re-examination revealed new information on the morphology of this taxon, including previously unknown parts of the Editor: Shree Ram Singh, National Cancer Institute, UNITED STATES skeleton such as the palate, braincase, and shoulder girdle. Elachistosuchus is diagnosed especially by the presence of the posterolateral process of the frontal, the extension of the Received: January 27, 2015 maxillary tooth row to the posterior margin of the orbit, the free posterior process of the Accepted: July 19, 2015 jugal, and the notched anterior margin of the interclavicle. Phylogenetic analyses using two Published: September 9, 2015 recently published character-taxon matrices recovered conflicting results for the phyloge- Copyright: This is an open access article, free of all netic position of Elachistosuchus–either as an archosauromorph, as a lepidosauromorph or copyright, and may be freely reproduced, distributed, as a more basal, non-saurian diapsid. -
An Early Late Triassic Long-Necked Reptile with a Bony Pectoral Shield and Gracile Appendages
An early Late Triassic long-necked reptile with a bony pectoral shield and gracile appendages JERZY DZIK and TOMASZ SULEJ Dzik, J. and Sulej, T. 2016. An early Late Triassic long-necked reptile with a bony pectoral shield and gracile appendages. Acta Palaeontologica Polonica 61 (4): 805–823. Several partially articulated specimens and numerous isolated bones of Ozimek volans gen. et sp. nov., from the late Carnian lacustrine deposits exposed at Krasiejów in southern Poland, enable a reconstruction of most of the skeleton. The unique character of the animal is its enlarged plate-like coracoids presumably fused with sterna. Other aspects of the skeleton seem to be comparable to those of the only known specimen of Sharovipteryx mirabilis from the latest Middle Triassic of Kyrgyzstan, which supports interpretation of both forms as protorosaurians. One may expect that the pectoral girdle of S. mirabilis, probably covered by the rock matrix in its only specimen, was similar to that of O. volans gen. et sp. nov. The Krasiejów material shows sharp teeth, low crescent scapula, three sacrals in a generalized pelvis (two of the sacrals being in contact with the ilium) and curved robust metatarsal of the fifth digit in the pes, which are unknown in Sharovipteryx. Other traits are plesiomorphic and, except for the pelvic girdle and extreme elongation of appendages, do not allow to identify any close connection of the sharovipterygids within the Triassic protorosaurians. Key words: Archosauromorpha, Sharovipteryx, protorosaurs, gliding, evolution, Carnian, Poland. Jerzy Dzik [[email protected]], Instytut Paleobiologii PAN, ul. Twarda 51/55, 00-818 Warszawa, Poland and Wydział Biologii Uniwersytetu Warszawskiego, Centrum Nauk Biologiczno-Chemicznych, ul. -
Reptile Family Tree - Peters 2017 1112 Taxa, 231 Characters
Reptile Family Tree - Peters 2017 1112 taxa, 231 characters Note: This tree does not support DNA topologies over 100 Eldeceeon 1990.7.1 67 Eldeceeon holotype long phylogenetic distances. 100 91 Romeriscus Diplovertebron Certain dental traits are convergent and do not define clades. 85 67 Solenodonsaurus 100 Chroniosaurus 94 Chroniosaurus PIN3585/124 Chroniosuchus 58 94 Westlothiana Casineria 84 Brouffia 93 77 Coelostegus Cheirolepis Paleothyris Eusthenopteron 91 Hylonomus Gogonasus 78 66 Anthracodromeus 99 Osteolepis 91 Protorothyris MCZ1532 85 Protorothyris CM 8617 81 Pholidogaster Protorothyris MCZ 2149 97 Colosteus 87 80 Vaughnictis Elliotsmithia Apsisaurus Panderichthys 51 Tiktaalik 86 Aerosaurus Varanops Greererpeton 67 90 94 Varanodon 76 97 Koilops <50 Spathicephalus Varanosaurus FMNH PR 1760 Trimerorhachis 62 84 Varanosaurus BSPHM 1901 XV20 Archaeothyris 91 Dvinosaurus 89 Ophiacodon 91 Acroplous 67 <50 82 99 Batrachosuchus Haptodus 93 Gerrothorax 97 82 Secodontosaurus Neldasaurus 85 76 100 Dimetrodon 84 95 Trematosaurus 97 Sphenacodon 78 Metoposaurus Ianthodon 55 Rhineceps 85 Edaphosaurus 85 96 99 Parotosuchus 80 82 Ianthasaurus 91 Wantzosaurus Glaucosaurus Trematosaurus long rostrum Cutleria 99 Pederpes Stenocybus 95 Whatcheeria 62 94 Ossinodus IVPP V18117 Crassigyrinus 87 62 71 Kenyasaurus 100 Acanthostega 94 52 Deltaherpeton 82 Galechirus 90 MGUH-VP-8160 63 Ventastega 52 Suminia 100 Baphetes Venjukovia 65 97 83 Ichthyostega Megalocephalus Eodicynodon 80 94 60 Proterogyrinus 99 Sclerocephalus smns90055 100 Dicynodon 74 Eoherpeton -
What Are Dinosaurs?
Tote Hughes, 140819 [email protected] Dinosaurs 1/20 What Are Dinosaurs? The following are not dinosaurs∗: • Things that aren’t organisms—There is no rock that is a dinosaur. • Things that existed before the Triassic period† • Pterosaurs The following are dinosaurs: • Birds (Aves) The following contain dinosaurs: • Archosaurs (X.Archosauria) • Reptiles (Reptilia) Dinosaur Overview A discussion of the important dinosaur clades. Dinosaurs are divided into two main groups: the eusaurischians‡ and ornithischians. Eusaurischians • Sauropods – Apatasaurus: diplodocoidean – Barosaurus: diplodocoidean – Brachiosaurus: macronarian – Diplodocus: diplodocoidean • Theropods – Allosaurus: carnosaurian – Archaeopteryx: maniraptor – Giganotosaurus: carnosaurian – Megalosaurus: megalosaurid – Spinosaurus: megalosaurid – Tyrannosaurus: tyrannosauroid – Velociraptor: maniraptor ∗See the Dinosaur Encyclopedia section for details on terms. †See Appendix: Time for details on geological time. ‡These are commonly called saurischians, but since almost every interesting saurischian is actually in the subclade X.Eusaurischia, I’ve taken the liberty of breaking the standard. I hope you will grow to understand and accept my decision. 1/20 Tote Hughes, 140819 [email protected] Dinosaurs 2/20 Ornithischians • Eurypodans (thyreophor) – Ankylosaurus: ankylosaurian – Stegosaurus: stegosaurian • Marginocephalians (cerapod) – Pachycephalosaurus: pachycephalosaurian – Triceratops: ceratopsian • Ornithopods (cerapod) – Hadrosaurus: hadrosauriform – Iguanodon: hadrosauriform -
A New Phylogenetic Analysis of Phytosauria (Archosauria: Pseudosuchia) with the Application of Continuous and Geometric Morphometric Character Coding
A new phylogenetic analysis of Phytosauria (Archosauria: Pseudosuchia) with the application of continuous and geometric morphometric character coding Andrew S. Jones and Richard J. Butler School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham, UK ABSTRACT Phytosauria is a clade of large, carnivorous, semi-aquatic archosauromorphs which reached its peak diversity and an almost global distribution in the Late Triassic (c. 230–201 Mya). Previous phylogenetic analyses of Phytosauria have either focused primarily on the relationships of specific subclades, or were limited in taxonomic scope, and no taxonomically comprehensive dataset is currently available. We here present the most taxonomically comprehensive cladistic dataset of phytosaurs to date, based on extensive first-hand study, identification of novel characters and synthesis of previous matrices. This results in an almost twofold increase in phylogenetic information scored per taxon over previous analyses. Alongside a traditional discrete character matrix, three variant matrices were analysed in which selected characters were coded using continuous and landmarking methods, to more rigorously explore phytosaur relationships. Based on these four data matrices, four tree topologies were recovered. Relationships among non-leptosuchomorph phytosaurs are largely consistent between these four topologies, whereas those of more derived taxa are more variable. Rutiodon carolinensis consistently forms a sister relationship with Angistorhinus. In three topologies Nicrosaurus nests deeply within a group of traditionally Submitted 24 April 2018 non-Mystriosuchini taxa, leading us to redefine Mystriosuchini by excluding 9 October 2018 Accepted Nicrosaurus as an internal specifier. Two distinct patterns of relationships within Published 10 December 2018 Mystriosuchini are present in the four topologies, distinguished largely by the Corresponding author Andrew S. -
A Large Predatory Archosaur from the Late Triassic of Poland
A large predatory archosaur from the Late Triassic of Poland GRZEGORZ NIEDŹWIEDZKI, TOMASZ SULEJ, and JERZY DZIK Niedźwiedzki, G., Sulej, T., and Dzik, J. 2012. A large predatory archosaur from the Late Triassic of Poland. Acta Palaeontologica Polonica 57 (2): 267–276. We describe a new large predatory archosaur, Smok wawelski gen. et sp. nov., from the latest Triassic (latest Norian–early Rhaetian; approximately 205–200 Ma) of Lisowice (Lipie Śląskie clay−pit) in southern Poland. The length of the recon− structed skeleton is 5–6 m and that of the skull 50–60 cm, making S. wawelski larger than any other known predatory archosaur from the Late Triassic and Early Jurassic of central Europe (including theropod dinosaurs and “rauisuchian” crurotarsans). The holotype braincase is associated with skull, pelvic and isolated limb−bones found in close proximity (within 30 m), and we regard them as belonging to the same individual. Large, apparently tridactyl tracks that occur in the same rock unit may have been left by animals of the same species. The highly autapomorphic braincase shows large at− tachment areas for hypertrophied protractor pterygoideus muscles on the lateral surface and a wide, funnel−like region be− tween the basal tubera and basipterygoid processes on the ventral surface. The skeleton (cranial and postcranial) pos− sesses some features similar to those in theropod dinosaurs and others to those in large crocodile−line archosaurs (“rauisuchians”), rendering phylogenetic placement of S. wawelski difficult at this time. Key words: Archosauria, “Rauisuchia”, Dinosauria, Norian–Rhaetian, Late Triassic, Poland. Grzegorz Niedźwiedzki [[email protected]], Institute of Zoology, University of Warsaw, ul. -
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 -
Now, on to Mesozoic Marine Reptiles
Now, on to Mesozoic Marine Reptiles NOT DINOSAURS! • They are reptiles, but some have adopted different skull fenestration • “Euryapsid” and “Anapsid” conditions are likely modified Diapsids • First reptiles returned to the sea in the Permian (Mesosaurus) How they are related: Sauropterygia Mosasauridae Thalattosuchia Dinosauria Phytosauria Lepidosauromorpha Crurotarsi Prolacertiformes Archosauromorpha Thalattosauriformes? Ichthyosauromorpha Sauria Claudiosaurus Neodiapsida Morphology • 4 basic body plans (Baupläne): (a) Thunniform advanced ichthyosaur (b) Long neck/small head plesiosaur (elasmosaur) (c) Short neck/big head pliosaur (d) Undulatory mosasaur (and basal ichthyosaur) • + “functional group 3” after Robert L. Carroll (“swimming lizards”) Morphological Trends • Limbs become rigid, often with hyperphalangy (many phalanges) • Polydactyly in ichthyosaurs Morphological Trends • (A) Merriamia (basal ichthyosaur) manus • (B) Opthalmosaurus (Jurassic ichthyosaur) manus • (C) Elasmosaurus (Cretaceous plesiosaur) manus • (D) Nothosaur pes • (E) Mosasaur pes Morphological Trends • Thoracic stiffening a usual trend • Lateral flexion directed posteriorly, or propulsion moved paraxially Carrier’s Constraint • Because of their sprawling gait, *GASP!* reptiles cannot breathe and run at the same time Ahhh… • Same applies to marine reptiles with lateral flexion (they breathe air!) *GASP!* • Solved by moving propulsion posteriorly, stiffening thorax, or moving limbs independently of spine Triassic Seas • Pangea beginning to break up • Marine