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Peerj-Review-5963
An unusual archosauromorph tooth increases known archosauromorph diversity in the Comment [1]: Be consistent with the clade you assign the tooth. lower portion of the Chinle Formation (Late Triassic) of southeastern Utah, USA Deleted: tetrapod Comment [2]: Is this formal? If so, Lopez, Andres; St. Aude, Isabella; Alderete, David; Alvarez, David; Aultman, Hannah; Busch, capitalize it. Comment [3]: Remember, readers from around the world could be citing you! Dominique; Bustamante, Rogelio; Cirks, Leah; Lopez, Martin; Moncada, Adriana; Ortega, Elizabeth; Verdugo, Carlos; Gay, Robert J *. Mission Heights Preparatory High School, 1376 E. Cottonwood Ln., Casa Grande, Arizona 85122 *[email protected] 520-836-9383 Abstract: An unusual tetrapod tooth was discovered in the Upper Triassic Chinle Formation of Deleted: Late southeastern Utah. The tooth was originally hypothesized to pertain to Revueltosaurus but Deleted: thought Deleted: belong further investigations have rejected that hypothesis. In this paper, we compare MNA V10668 to other known fossil teeth found in the Chinle Formation and assign the tooth to the least inclusive Comment [4]: Use tooth crowns (there is no root) throughout the text. clade currently available. Using data found in other publications and pictures of other teeth, we Deleted: identify Deleted: it may belongs to compare this specimen to other Triassic dental taxa. MNA V10668 shares some similarities with Crosbysaurus, Tecovasaurus, and several other named taxa but possesses a unique combination Deleted: characteristics of characteristics not found in other archosauromorph teeth. We conclude that it is most likely an Deleted: diapsid archosauromorph and possibly an archosauriform. This increases the known diversity of Deleted: probably archosauromorph from the Chinle Formation and represents the first tooth morphotype Deleted: tetrapods completely unique to Utah in the Late Triassic. -
First Palaeohistological Inference of Resting
First palaeohistological inference of resting metabolic rate in an extinct synapsid, Moghreberia nmachouensis (Therapsida: Anomodontia) Chloe Olivier, Alexandra Houssaye, Nour-Eddine Jalil, Jorge Cubo To cite this version: Chloe Olivier, Alexandra Houssaye, Nour-Eddine Jalil, Jorge Cubo. First palaeohistological inference of resting metabolic rate in an extinct synapsid, Moghreberia nmachouensis (Therapsida: Anomodon- tia). Biological Journal of the Linnean Society, Linnean Society of London, 2017, 121 (2), pp.409-419. 10.1093/biolinnean/blw044. hal-01625105 HAL Id: hal-01625105 https://hal.sorbonne-universite.fr/hal-01625105 Submitted on 27 Oct 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. First palaeohistological inference of resting metabolic rate in extinct synapsid, Moghreberia nmachouensis (Therapsida: Anomodontia) CHLOE OLIVIER1,2, ALEXANDRA HOUSSAYE3, NOUR-EDDINE JALIL2 and JORGE CUBO1* 1 Sorbonne Universités, UPMC Univ Paris 06, CNRS, UMR 7193, Institut des Sciences de la Terre Paris (iSTeP), 4 place Jussieu, BC 19, 75005, Paris, France 2 Sorbonne Universités -CR2P -MNHN, CNRS, UPMC-Paris6. Muséum national d’Histoire naturelle. 57 rue Cuvier, CP38. F-75005, Paris, France 3Département Écologie et Gestion de la Biodiversité, UMR 7179, CNRS/Muséum national d’Histoire naturelle, 57 rue Cuvier, CP 55, Paris, 75005, France *Corresponding author. -
8. Archosaur Phylogeny and the Relationships of the Crocodylia
8. Archosaur phylogeny and the relationships of the Crocodylia MICHAEL J. BENTON Department of Geology, The Queen's University of Belfast, Belfast, UK JAMES M. CLARK* Department of Anatomy, University of Chicago, Chicago, Illinois, USA Abstract The Archosauria include the living crocodilians and birds, as well as the fossil dinosaurs, pterosaurs, and basal 'thecodontians'. Cladograms of the basal archosaurs and of the crocodylomorphs are given in this paper. There are three primitive archosaur groups, the Proterosuchidae, the Erythrosuchidae, and the Proterochampsidae, which fall outside the crown-group (crocodilian line plus bird line), and these have been defined as plesions to a restricted Archosauria by Gauthier. The Early Triassic Euparkeria may also fall outside this crown-group, or it may lie on the bird line. The crown-group of archosaurs divides into the Ornithosuchia (the 'bird line': Orn- ithosuchidae, Lagosuchidae, Pterosauria, Dinosauria) and the Croco- dylotarsi nov. (the 'crocodilian line': Phytosauridae, Crocodylo- morpha, Stagonolepididae, Rauisuchidae, and Poposauridae). The latter three families may form a clade (Pseudosuchia s.str.), or the Poposauridae may pair off with Crocodylomorpha. The Crocodylomorpha includes all crocodilians, as well as crocodi- lian-like Triassic and Jurassic terrestrial forms. The Crocodyliformes include the traditional 'Protosuchia', 'Mesosuchia', and Eusuchia, and they are defined by a large number of synapomorphies, particularly of the braincase and occipital regions. The 'protosuchians' (mainly Early *Present address: Department of Zoology, Storer Hall, University of California, Davis, Cali- fornia, USA. The Phylogeny and Classification of the Tetrapods, Volume 1: Amphibians, Reptiles, Birds (ed. M.J. Benton), Systematics Association Special Volume 35A . pp. 295-338. Clarendon Press, Oxford, 1988. -
The Origin and Early Evolution of Dinosaurs
Biol. Rev. (2010), 85, pp. 55–110. 55 doi:10.1111/j.1469-185X.2009.00094.x The origin and early evolution of dinosaurs Max C. Langer1∗,MartinD.Ezcurra2, Jonathas S. Bittencourt1 and Fernando E. Novas2,3 1Departamento de Biologia, FFCLRP, Universidade de S˜ao Paulo; Av. Bandeirantes 3900, Ribeir˜ao Preto-SP, Brazil 2Laboratorio de Anatomia Comparada y Evoluci´on de los Vertebrados, Museo Argentino de Ciencias Naturales ‘‘Bernardino Rivadavia’’, Avda. Angel Gallardo 470, Cdad. de Buenos Aires, Argentina 3CONICET (Consejo Nacional de Investigaciones Cient´ıficas y T´ecnicas); Avda. Rivadavia 1917 - Cdad. de Buenos Aires, Argentina (Received 28 November 2008; revised 09 July 2009; accepted 14 July 2009) ABSTRACT The oldest unequivocal records of Dinosauria were unearthed from Late Triassic rocks (approximately 230 Ma) accumulated over extensional rift basins in southwestern Pangea. The better known of these are Herrerasaurus ischigualastensis, Pisanosaurus mertii, Eoraptor lunensis,andPanphagia protos from the Ischigualasto Formation, Argentina, and Staurikosaurus pricei and Saturnalia tupiniquim from the Santa Maria Formation, Brazil. No uncontroversial dinosaur body fossils are known from older strata, but the Middle Triassic origin of the lineage may be inferred from both the footprint record and its sister-group relation to Ladinian basal dinosauromorphs. These include the typical Marasuchus lilloensis, more basal forms such as Lagerpeton and Dromomeron, as well as silesaurids: a possibly monophyletic group composed of Mid-Late Triassic forms that may represent immediate sister taxa to dinosaurs. The first phylogenetic definition to fit the current understanding of Dinosauria as a node-based taxon solely composed of mutually exclusive Saurischia and Ornithischia was given as ‘‘all descendants of the most recent common ancestor of birds and Triceratops’’. -
Wonderful Wacky Water Critters
Wonderful, Wacky, Water Critters WONDERFUL WACKY WATER CRITTERS HOW TO USE THIS BOOK 1. The “KEY TO MACROINVERTEBRATE LIFE IN THE RIVER” or “KEY TO LIFE IN THE POND” identification sheets will help you ‘unlock’ the name of your animal. 2. Look up the animal’s name in the index in the back of this book and turn to the appropriate page. 3. Try to find out: a. What your animal eats. b. What tools it has to get food. c. How it is adapted to the water current or how it gets oxygen. d. How it protects itself. 4. Draw your animal’s adaptations in the circles on your adaptation worksheet on the following page. GWQ023 Wonderful Wacky Water Critters DNR: WT-513-98 This publication is available from county UW-Extension offices or from Extension Publications, 45 N. Charter St., Madison, WI 53715. (608) 262-3346, or toll-free 877-947-7827 Lead author: Suzanne Wade, University of Wisconsin–Extension Contributing scientists: Phil Emmling, Stan Nichols, Kris Stepenuck (University of Wisconsin–Extension) and Mike Miller, Mike Sorge (Wisconsin Department of Natural Resources) Adapted with permission from a booklet originally published by Riveredge Nature Center, Newburg, WI, Phone 414/675-6888 Printed on Recycled Paper Illustrations by Carolyn Pochert and Lynne Bergschultz Page 1 CRITTER ADAPTATION CHART How does it get its food? How does it get away What is its food? from enemies? Draw your “critter” here NAME OF “CRITTER” How does it get oxygen? Other unique adaptations. Page 2 TWO COMMON LIFE CYCLES: WHICH METHOD OF GROWING UP DOES YOUR ANIMAL HAVE? egg larva adult larva - older (mayfly) WITHOUT A PUPAL STAGE? THESE ANIMALS GROW GRADUALLY, CHANGING ONLY SLIGHTLY AS THEY GROW UP. -
Late Triassic) Adrian P
New Mexico Geological Society Downloaded from: http://nmgs.nmt.edu/publications/guidebooks/56 Definition and correlation of the Lamyan: A new biochronological unit for the nonmarine Late Carnian (Late Triassic) Adrian P. Hunt, Spencer G. Lucas, and Andrew B. Heckert, 2005, pp. 357-366 in: Geology of the Chama Basin, Lucas, Spencer G.; Zeigler, Kate E.; Lueth, Virgil W.; Owen, Donald E.; [eds.], New Mexico Geological Society 56th Annual Fall Field Conference Guidebook, 456 p. This is one of many related papers that were included in the 2005 NMGS Fall Field Conference Guidebook. Annual NMGS Fall Field Conference Guidebooks Every fall since 1950, the New Mexico Geological Society (NMGS) has held an annual Fall Field Conference that explores some region of New Mexico (or surrounding states). Always well attended, these conferences provide a guidebook to participants. Besides detailed road logs, the guidebooks contain many well written, edited, and peer-reviewed geoscience papers. These books have set the national standard for geologic guidebooks and are an essential geologic reference for anyone working in or around New Mexico. Free Downloads NMGS has decided to make peer-reviewed papers from our Fall Field Conference guidebooks available for free download. Non-members will have access to guidebook papers two years after publication. Members have access to all papers. This is in keeping with our mission of promoting interest, research, and cooperation regarding geology in New Mexico. However, guidebook sales represent a significant proportion of our operating budget. Therefore, only research papers are available for download. Road logs, mini-papers, maps, stratigraphic charts, and other selected content are available only in the printed guidebooks. -
01 Oliveira & Pinheiro RBP V20 N2 COR.Indd
Rev. bras. paleontol. 20(2):155-162, Maio/Agosto 2017 © 2017 by the Sociedade Brasileira de Paleontologia doi: 10.4072/rbp.2017.2.01 ISOLATED ARCHOSAURIFORM TEETH FROM THE UPPER TRIASSIC CANDELÁRIA SEQUENCE (HYPERODAPEDON ASSEMBLAGE ZONE, SOUTHERN BRAZIL) TIANE MACEDO DE OLIVEIRA & FELIPE L. PINHEIRO Laboratório de Paleobiologia, Universidade Federal do Pampa, Campus São Gabriel, R. Aluízio Barros Macedo, BR 290, km 423, 97300-000, São Gabriel, RS, Brazil. [email protected], [email protected] ABSTRACT – We describe isolated teeth found in the locality “Sítio Piveta” (Hyperodapedon Assemblage Zone, Candelaria Sequence, Upper Triassic of the Paraná Basin). The material consists of five specimens, here classified into three different morphotypes. The morphotype I is characterized by pronounced elongation, rounded base and symmetry between lingual and labial surfaces. The morphotype II presents serrated mesial and distal edges, mesial denticles decreasing in size toward the base, distal denticles present until the base and asymmetry, with a flat lingual side and rounded labial side. The morphotype III, although similar to morphotype II, has a greater inclination of the posterior carinae. The conservative dental morphology in Archosauriformes makes difficult an accurate taxonomic assignment based only on isolated teeth. However, the specimens we present are attributable to “Rauisuchia” (morphotype II and III) and, possibly, Phytosauria (morphotype I). The putative presence of a phytosaur in the Carnian Hyperodapedon Assemblage Zone would have impact in the South American distribution of the group. The taxonomic assignments proposed herein contribute to the faunal composition of the Hyperodapedon Assemblage Zone, a critical unit on the study of the Upper Triassic radiation of archosaurs. -
On the Presence of the Subnarial Foramen in Prestosuchus Chiniquensis (Pseudosuchia: Loricata) with Remarks on Its Phylogenetic Distribution
Anais da Academia Brasileira de Ciências (2016) (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 http://dx.doi.org/10.1590/0001-3765201620150456 www.scielo.br/aabc On the presence of the subnarial foramen in Prestosuchus chiniquensis (Pseudosuchia: Loricata) with remarks on its phylogenetic distribution LÚCIO ROBERTO-DA-SILVA1,2, MARCO A.G. FRANÇA3, SÉRGIO F. CABREIRA3, RODRIGO T. MÜLLER1 and SÉRGIO DIAS-DA-SILVA4 ¹Programa de Pós-Graduação em Biodiversidade Animal, Universidade Federal de Santa Maria, Av. Roraima, 1000, Bairro Camobi, 97105-900 Santa Maria, RS, Brasil ²Laboratório de Paleontologia, Universidade Luterana do Brasil, Av. Farroupilha, 8001, Bairro São José, 92425-900 Canoas, RS, Brasil ³Laboratório de Paleontologia e Evolução de Petrolina, Campus de Ciências Agrárias, Universidade Federal do Vale do São Francisco, Rodovia BR 407, Km12, Lote 543, 56300-000 Petrolina, PE, Brasil 4Centro de Apoio à Pesquisa da Quarta Colônia, Universidade Federal de Santa Maria, Rua Maximiliano Vizzotto, 598, 97230-000 São João do Polêsine, RS, Brasil Manuscript received on July 1, 2015; accepted for publication on April 15, 2016 ABSTRACT Many authors have discussed the subnarial foramen in Archosauriformes. Here presence among Archosauriformes, shape, and position of this structure is reported and its phylogenetic importance is investigated. Based on distribution and the phylogenetic tree, it probably arose independently in Erythrosuchus, Herrerasaurus, and Paracrocodylomorpha. In Paracrocodylomorpha the subnarial foramen is oval-shaped, placed in the middle height of the main body of the maxilla, and does not reach the height of ascending process. In basal loricatans from South America (Prestosuchus chiniquensis and Saurosuchus galilei) the subnarial foramen is ‘drop-like’ shaped, the subnarial foramen is located above the middle height of the main body of the maxilla, reaching the height of ascending process, a condition also present in Herrerasaurus ischigualastensis. -
New Insights on Prestosuchus Chiniquensis Huene
New insights on Prestosuchus chiniquensis Huene, 1942 (Pseudosuchia, Loricata) based on new specimens from the “Tree Sanga” Outcrop, Chiniqua´ Region, Rio Grande do Sul, Brazil Marcel B. Lacerda1, Bianca M. Mastrantonio1, Daniel C. Fortier2 and Cesar L. Schultz1 1 Instituto de Geocieˆncias, Laborato´rio de Paleovertebrados, Universidade Federal do Rio Grande do Sul–UFRGS, Porto Alegre, Rio Grande do Sul, Brazil 2 CHNUFPI, Campus Amı´lcar Ferreira Sobral, Universidade Federal do Piauı´, Floriano, Piauı´, Brazil ABSTRACT The ‘rauisuchians’ are a group of Triassic pseudosuchian archosaurs that displayed a near global distribution. Their problematic taxonomic resolution comes from the fact that most taxa are represented only by a few and/or mostly incomplete specimens. In the last few decades, renewed interest in early archosaur evolution has helped to clarify some of these problems, but further studies on the taxonomic and paleobiological aspects are still needed. In the present work, we describe new material attributed to the ‘rauisuchian’ taxon Prestosuchus chiniquensis, of the Dinodontosaurus Assemblage Zone, Middle Triassic (Ladinian) of the Santa Maria Supersequence of southern Brazil, based on a comparative osteologic analysis. Additionally, we present well supported evidence that these represent juvenile forms, due to differences in osteological features (i.e., a subnarial fenestra) that when compared to previously described specimens can be attributed to ontogeny and indicate variation within a single taxon of a problematic but important -
Xenacanthus (Chondrichthyes: Xenacanthiformes) from North America
Acta Geologica Polonica, Vol. 49 (J 999), No.3, pp. 215-266 406 IU S UNES 0 I Dentitions of Late Palaeozoic Orthacanthus species and new species of ?Xenacanthus (Chondrichthyes: Xenacanthiformes) from North America GARY D. JOHNSON Department of Earth Sciences and Physics, University of South Dakota; 414 East Clark Street, Vermillion, SD 57069-2390, USA. E-mail: [email protected] ABSTRACT: JOHNSON, G.D. 1999. Dentitions of Late Palaeozoic Orthacanthus species and new species of ?Xenacanthus (Chondrichthyes: Xenacanthiformes) from North America. Acta Geologica Polonica, 49 (3),215-266. Warszawa. Orthacanthus lateral teeth have paired, variably divergent, smooth, usually carinated labio-lingually compressed principal cusps separated by a central foramen; one or more intermediate cusps; and an api cal button on the base isolated from the cusps. Several thousand isolated teeth from Texas Artinskian bulk samples are used to define the heterodont dentitions of O. texensis and O. platypternus. The O. tex ensis tooth base has a labio-Iingual width greater than the anteromedial-posterolateral length, the basal tubercle is restricted to the thick labial margin, the principal cusps are serrated to varying degrees, and the posterior cusp is larger. The O. platypternus tooth base is longer than wide, its basal tubercle extends to the center, the labial margin is thin, serrations are absent on the principal cusps, the anterior cusp is larger, and a single intermediate cusp is present. More than two hundred isolated teeth from Nebraska (Gzhelian) and Pennsylvania (Asselian) provide a preliminary description of the heterodont dentition of O. compress us . The principal cusps are similar to O. -
C05 A4 BP Placerias
ArtNr: C05 ArtNr: C05 ArtNr: C05 Placerias gigas Placerias Placerias gigas gigas 0DVWDEVFDOH 0DVWDEVFDOH 1/72 1/72 Placerias gigas 1/72 Placerias war ein etwa 3m langer Cynodont der mittleren Trias. Als Therapside ist er kein Dinosaurier, aber ein Zeitgenosse der aufkommenden Dinosaurier. P. lebte in Herden und IKUWH wahrscheinlich ein semiaquatisches Leben lKQOLFK den 0DVWDEVFDOH heutigen Flusspferden. 1/72 L:5 cm, B/W:1,9 cm, H:2,5 cm Kelenken was a 3m long Cynodont of the middle Triassic. As a Therapsid it had been a contempory of long skull. The so called Terrorbirds were the top-predators $%¡+50,;960,1,0$;$'00;,9$49$(0$77,$&2590*(50$1,$ of Patagonia. Their recent relatives are the Seriemas. Terrorbirds caught there prey by knocking them out of balance or stabbing them with their giant beaks. 0DVWDEVFDOH ArtNr: C05 1/72 0DVWDEVFDOH Placerias gigas 1/72 Placerias gigas Einzelteile: 2 Kleber, Farben und Bauanleitung - assembly instruction Gras sind nicht ent- halten Parts: 2 Glue, colours and gras are not included I Ol An La Ka Trias/ Triassic No Rh -252,2 Ma -247,2 -242 -235 -228 -222 -215 -208,5 -201,3 Kannemeyeriiformes Placerias (# 1) Stahleckeriidae Stahlecker- Einzelteile/Parts: iinae [.|USHUERG\ Placeriinae Zambiasaurus 1 x Grundplatte/base (# III) Placerias Moghreberia Kladogramm: Kammerer, 2013 I] 9HUVlXEHUQGHU*XQlKWH I] Remove casting seam, cut Placerias gigas (Lucas, 1904) DEWUHQQHQGHU*XlVWHEHL off sprues, resculpting if Bedarf nachmodellieren necessary Lebenszeit/Lifespan : mittleres Norium/middle Norian (222-215 Ma) Verbreitung/Distribution : USA, Afrika II] Bemalung II] Painting /lQJHOHQJKW: 3 m (UQlKUXQJ'LHW : herbivor Habitat: semiaquatic III] Montage auf Grundplatte III] Fix on base Paleofauna: Postosuchus, Coelophysis, Phytosauria $%¡+50,;960,1,0$;$'00;9$49$(0$77,$&2590*(50$1,$ Paleoflora%DXPIDUQH&\DWKHDOHV%lUODSSSIODQ]HQ/\FRSRGLRSVLGD ArtNr: C05 ArtNr: C05 ArtNr: C05 Placerias gigas Placerias Placerias gigas gigas 0DVWDEVFDOH 0DVWDEVFDOH 1/72 1/72 Placerias gigas 1/72 Placerias war ein etwa 3m langer Cynodont der mittleren Trias. -
Crustaceans Body Only Was ~2’ Long, Claw Was an Additional 20”
Crustaceans body only was ~2’ long, claw was an additional 20” =shelled creatures; “the insects of the sea” ! ~ 4’ long total some crustaceans are quite colorful; blue, red, ~67,000 species orange, yellow eg: lobsters, crayfish, shrimp, crabs, water fleas, many are bioluminescent copepods, barnacles, pill bugs, etc A. crustaceans are mostly aquatic, the great majority vary in size from microscopic (<0.1 mm) to 12’ are marine some crustaceans live for several decades; some inhabit most waters of the earth: ocean , arctic , freshwaters, molt throughout life high mountain creeks and lakes thermal springs, brine waters so continuous increase in size 1. many are benthic eg. crayfish & freshwater shrimp eg. especially the larger crustaceans; shrimp and crabs largest crustaceans in freshwaters eg. also isopods, amphipods some up to 2’ and weigh 9 lbs e. Ostracoda (=seed shrimp) a river shrimp, Macrobrachium jamaicense, was collected from Devils River, Tx: body was 10.5” common in freshwater and marine habitats long, 3’ long including antennae, 3 lbs mainly benthic animals that inhabit all types of eg largest (longest) is giant Japanese crab substrates in standing and running water ! up to 12’ from end of claws to tail and a weight of a few actively swim just above the substrate 40 lbs (20 kg) generally use their antennae to move Lobsters may be the longest lived Crustaceans enclosed in bivalve carapace that completely covers one was collected that weighed 35 lbs the entire animal was estimated to be 50 yrs old; Animals: Arthropoda - Crustacea;