Palaeontological Study of the Rystkuil Channel
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Reptile-Like Physiology in Early Jurassic Stem-Mammals
bioRxiv preprint doi: https://doi.org/10.1101/785360; this version posted October 10, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Title: Reptile-like physiology in Early Jurassic stem-mammals Authors: Elis Newham1*, Pamela G. Gill2,3*, Philippa Brewer3, Michael J. Benton2, Vincent Fernandez4,5, Neil J. Gostling6, David Haberthür7, Jukka Jernvall8, Tuomas Kankanpää9, Aki 5 Kallonen10, Charles Navarro2, Alexandra Pacureanu5, Berit Zeller-Plumhoff11, Kelly Richards12, Kate Robson-Brown13, Philipp Schneider14, Heikki Suhonen10, Paul Tafforeau5, Katherine Williams14, & Ian J. Corfe8*. Affiliations: 10 1School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK. 2School of Earth Sciences, University of Bristol, Bristol, UK. 3Earth Science Department, The Natural History Museum, London, UK. 4Core Research Laboratories, The Natural History Museum, London, UK. 5European Synchrotron Radiation Facility, Grenoble, France. 15 6School of Biological Sciences, University of Southampton, Southampton, UK. 7Institute of Anatomy, University of Bern, Bern, Switzerland. 8Institute of Biotechnology, University of Helsinki, Helsinki, Finland. 9Department of Agricultural Sciences, University of Helsinki, Helsinki, Finland. 10Department of Physics, University of Helsinki, Helsinki, Finland. 20 11Helmholtz-Zentrum Geesthacht, Zentrum für Material-und Küstenforschung GmbH Germany. 12Oxford University Museum of Natural History, Oxford, OX1 3PW, UK. 1 bioRxiv preprint doi: https://doi.org/10.1101/785360; this version posted October 10, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 13Department of Anthropology and Archaeology, University of Bristol, Bristol, UK. 14Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, UK. -
Femur of a Morganucodontid Mammal from the Middle Jurassic of Central Russia
Femur of a morganucodontid mammal from the Middle Jurassic of Central Russia PETR P. GAMBARYAN and ALEXANDER 0.AVERIANOV Gambaryan, P.P. & Averianov, A.O. 2001. Femur of a morganucodontid mammal from the Middle Jurassic of Central Russia. -Acta Palaeontologica Polonica 46,1,99-112. We describe a nearly complete mammalian femur from the Middle Jurassic (upper Bathonian) from Peski quarry, situated some 100 km south east of Moscow, central Rus- sia. It is similar to the femora of Morganucodontidae in having a globular femoral head, separated from the greater trochanter and reflected dorsally, fovea capitis present, both trochanters triangular and located on the same plane, distal end flat, mediolaterally expanded, and somewhat bent ventrally, and in the shape and proportions of distal condyles. It is referred to as Morganucodontidae gen. et sp. indet. It is the first representa- tive of this group of mammals in Eastern Europe from the third Mesozoic mammal local- ity discovered in Russia. Exquisite preservation of the bone surface allowed us to recon- struct partial hind limb musculature. We reconstruct m. iliopsoas as inserting on the ridge, which starts at the lesser trochanter and extends along the medial femoral margin for more than half of the femur length. On this basis we conclude that the mode of loco- motion of the Peski morganucodontid was similar to that of modern echidnas. During the propulsive phase the femur did not retract and the step elongation was provided by pronation of the femur. Key words : Mammalia, Morganucodontidae, femur, anatomy, locomotion, Jurassic, Russia. Petr P. Gambaryan [[email protected]] and Alexander 0. -
A New Mammaliaform from the Early Jurassic and Evolution Of
R EPORTS tary trough with a shelflike dorsal medial ridge, and all other nonmammalian mamma- A New Mammaliaform from the liaforms have a medial concavity on the man- dibular angle (8–14, 23), as in nonmamma- Early Jurassic and Evolution of liaform cynodonts (9, 14, 24–27). The post- dentary trough and the medial concavity on Mammalian Characteristics the mandibular angle respectively accommo- dated the prearticular/surangular and the re- Zhe-Xi Luo,1* Alfred W. Crompton,2 Ai-Lin Sun3 flected lamina of the angular (9, 25–27) that are the homologs to the mammalian middle A fossil from the Early Jurassic (Sinemurian, ϳ195 million years ago) represents ear bones (9, 14, 16–21, 23, 26). The absence a new lineage of mammaliaforms, the extinct groups more closely related to of these structures indicates that the postden- the living mammals than to nonmammaliaform cynodonts. It has an enlarged tary bones (“middle ear ossicles”) must have cranial cavity, but no postdentary trough on the mandible, indicating separation been separated from the mandible (Fig. 3). of the middle ear bones from the mandible. This extends the earliest record of Hadrocodium lacks the primitive meckelian these crucial mammalian features by some 45 million years and suggests that sulcus of the mandible typical of all nonmam- separation of the middle ear bones from the mandible and the expanded brain maliaform cynodonts (24–27), stem groups vault could be correlated. It shows that several key mammalian evolutionary of mammaliaforms (8, 9, 14, 23, 26, 27), innovations in the ear region, the temporomandibular joint, and the brain vault triconodontids (28, 29), and nontribosphenic evolved incrementally through mammaliaform evolution and long before the therian mammals (30). -
Mesozoic: the Dark Age for Mammals!
Ed’s Simplified History of the Mammals Note progression from Pelycosaurs (1) to Therapsids and Cynodonts (2) in Triassic. Stem mammals appeared in Late Triassic and Early Jurassic (3). Relationships among the Middle Jurassic forms (4) are controversial (see handout). Therian clade, identified by the tribosphenic molar (5), emerged at the end of the Jurassic, Early Cretaceous. A slightly more detailed version… in case you like something that looks more slick From Pough et al. 2009. Vertebrate Life, 8th ed. Pelycosaurs Dominated the late Permian, gave rise to therapsids Therapsids Rapid radiation in late Permian, around 270 MYA Still “mammal-like reptiles” The mass extinction at the end of the Permian was the greatest loss of diversity ever with >80% of all known genera and about 90% of all species going extinct, both terrestrial and marine. Cynodonts Late Permian to mid Triassic Last remaining group of therapsids, survived mass extinction at the end of the Permian. Persisted well Only 1 lineage of into Triassic and developed cynodonts survived many features associated through the late Triassic, with mammals. and this group became ancestors of mammals. Mesozoic: the Dark Age for Mammals! multituberculate Morganucodon, one of the earliest mammals (What else was happening in the Late Triassic and Jurassic Hadrocodium that may have contributed to mammals becoming small and Most were very small with nocturnal?) conservative morphology ...but new fossil finds indicate more diversity than we thought Repenomanus Still, largest known mammal during Mesozic Most were shrew to is no larger than a mouse sized, for 125 woodchuck million years! Some Mesozoic events and mammals you should know 1. -
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. -
Origin and Relationships of the Ictidosauria to Non-Mammalian
Historical Biology An International Journal of Paleobiology ISSN: 0891-2963 (Print) 1029-2381 (Online) Journal homepage: http://www.tandfonline.com/loi/ghbi20 Origin and relationships of the Ictidosauria to non- mammalian cynodonts and mammals José F. Bonaparte & A. W. Crompton To cite this article: José F. Bonaparte & A. W. Crompton (2017): Origin and relationships of the Ictidosauria to non-mammalian cynodonts and mammals, Historical Biology, DOI: 10.1080/08912963.2017.1329911 To link to this article: http://dx.doi.org/10.1080/08912963.2017.1329911 Published online: 23 Jun 2017. Submit your article to this journal Article views: 53 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=ghbi20 Download by: [Smithsonian Astrophysics Observatory] Date: 06 November 2017, At: 13:06 HISTORICAL BIOLOGY, 2017 https://doi.org/10.1080/08912963.2017.1329911 Origin and relationships of the Ictidosauria to non-mammalian cynodonts and mammals José F. Bonapartea and A. W. Cromptonb aMuseo Municipal de C. Naturales “C. Ameghino”, Mercedes, Argentina; bMuseum of Comparative Zoology, Harvard University, Cambridge, MA, USA ABSTRACT ARTICLE HISTORY Ictidosaurian genera are allocated to two families, Tritheledontidae and Therioherpetidae. This paper Received 19 December 2016 provides a diagnosis for Ictidosauria. The previously named family Brasilodontidae is shown to be a Accepted 30 April 2017 junior synonym of a family, Therioherpetidae. It is concluded that Ictidosauria originated from Late KEYWORDS Permian procynosuchid non-mammalian cynodonts rather than from Middle Triassic probainognathid Mammalian origins; non-mammalian cynodonts. The structure of the skull and jaws of a derived traversodontid Ischignathus Ictidosauria; Tritylodontia; sudamericanus from the early Late Triassic of Argentina supports an earlier view that tritylodontids are Brasilitherium more closely related to traversodontid than probainognathid non-mammalian cynodonts. -
Mammal Disparity Decreases During the Cretaceous Angiosperm Radiation
Mammal disparity decreases during the Cretaceous angiosperm radiation David M. Grossnickle1 and P. David Polly2 1Department of Geological Sciences, and 2Departments of Geological Sciences, Biology, and Anthropology, rspb.royalsocietypublishing.org Indiana University, Bloomington, IN 47405, USA Fossil discoveries over the past 30 years have radically transformed tra- ditional views of Mesozoic mammal evolution. In addition, recent research provides a more detailed account of the Cretaceous diversification of flower- Research ing plants. Here, we examine patterns of morphological disparity and functional morphology associated with diet in early mammals. Two ana- Cite this article: Grossnickle DM, Polly PD. lyses were performed: (i) an examination of diversity based on functional 2013 Mammal disparity decreases during dental type rather than higher-level taxonomy, and (ii) a morphometric analysis of jaws, which made use of modern analogues, to assess changes the Cretaceous angiosperm radiation. Proc R in mammalian morphological and dietary disparity. Results demonstrate a Soc B 280: 20132110. decline in diversity of molar types during the mid-Cretaceous as abundances http://dx.doi.org/10.1098/rspb.2013.2110 of triconodonts, symmetrodonts, docodonts and eupantotherians dimin- ished. Multituberculates experience a turnover in functional molar types during the mid-Cretaceous and a shift towards plant-dominated diets during the late Late Cretaceous. Although therians undergo a taxonomic Received: 13 August 2013 expansion coinciding with the angiosperm radiation, they display small Accepted: 12 September 2013 body sizes and a low level of morphological disparity, suggesting an evol- utionary shift favouring small insectivores. It is concluded that during the mid-Cretaceous, the period of rapid angiosperm radiation, mammals experi- enced both a decrease in morphological disparity and a functional shift in dietary morphology that were probably related to changing ecosystems. -
Diagnosis of the Class Mammalia
FAUNA of AUSTRALIA 14. DIAGNOSIS OF THE CLASS MAMMALIA WILLIAM A. CLEMENS 1 14. DIAGNOSIS OF THE CLASS MAMMALIA 2 14. DIAGNOSIS OF THE CLASS MAMMALIA INTRODUCTION These days, the production of new definitions of the Class Mammalia appears to be a healthy cottage industry. The products vary according to the different philosophies of classification espoused by their authors and the applications for which they are intended. Here, I shall discuss classifications that may be appropriate for two different types of inquiries: First are definitions of the Class for the purposes of comparing members of the Mammalia with members of other groups of comparable rank, especially Reptilia or Aves. Assessment of the fidelity with which a classification represents patterns and rates of evolution is particularly important when studies emphasise comparison of characters of modern members of the classes. Second, other definitions have been proposed for the purpose of circumscribing the Mammalia and distinguishing its membership from the animals that usually are dubbed the ‘mammal-like reptiles’. These commonly are based on a foundation made up of the living mammals – monotremes, marsupials and eutherians. Then, on different criteria, related prehistoric species are included. In some, membership is strictly defined to include only modern mammals, their last common ancestor and members of all extinct lineages derived from that common ancestor. Other definitions have been variously designed to recognise the origin of a mammalian grade of evolution, typus or Bauplan with a specific character or suite of characters arbitrarily chosen to define membership. A survey of the classifications produced by these different approaches shows that in both the apparent common ancestors of all living mammals usually are included in the Class. -
Reptilian, Therapsid and Mammalian Teeth from the Upper Triassic of Varangéville (Northeastern France) by Pascal GODEFROIT
bulletin de l'institut royal des sciences naturelles de belgique sciences de la terre, 67: 83-102, 1997 bulletin van het koninklijk belgisch instituut voor natuurwetenschappen aardwetenschappen, 67: 83-102, 1997 Reptilian, therapsid and mammalian teeth from the Upper Triassic of Varangéville (northeastern France) by Pascal GODEFROIT Abstract isolated teeth, representing five mammalian families. Until recently, mammals were very rare in other localities Microvertebrate remains have been discovered at a new Late Triassic of the Paris Basin and, with rare exceptions, consisted locality in Varangéville (northeastern France). The material includes reptilian (Ichthyosauria indet., Phytosauridae indet., the pterosaur aff. mainly of Haramiyidae. Maubeuge (1955: 124) describes Eudimorphodon, Archosauria indet.), therapsid (advanced Cynodontia) a bone bed in the lower Rhaetian of Varangéville. At the and mammalian (Haramiyidae, Morganucodontidae, Sinoconodonti- present time, only fish teeth have been found in this layer dae and Woutersiidae) teeth, described in the present paper. The faunal composition, closely resembling that of the neighbouring locality of (pers. obs.). In Saint-Nicolas-de-Port, suggests a coastal or a deltaic depositional April 1995, Michel Ulrich, owner of a patch of land environment. in the vicinity of Varangéville, drew the author's atten¬ tion to the presence of fossil bones on his land. He Key-words: Reptiles, therapsids, mammals, teeth, Upper Triassic, very Varangéville. kindly authorized the Institut royal des Sciences natu¬ relles de Belgique to start excavations there. The sédi¬ ments were carefully washed and screened and the micro- remains were Résumé subsequently sorted under a binocular. This led to the discovery of a collection of isolated bones and teeth of Late Triassic vertebrates. -
Cynodontia, Chiniquodontidae) from the Brazilian Middle Triassic
Rev. bras. paleontol. 12(2):113-122, Maio/Agosto 2009 © 2009 by the Sociedade Brasileira de Paleontologia doi:10.4072/rbp.2009.2.02 A PARTIAL SKELETON OF CHINIQUODON (CYNODONTIA, CHINIQUODONTIDAE) FROM THE BRAZILIAN MIDDLE TRIASSIC TÉO VEIGA DE OLIVEIRA, CESAR LEANDRO SCHULTZ & MARINA BENTO SOARES Departamento de Paleontologia e Estratigrafia, IGEO, UFRGS, Cx. P. 15001, 91501-970, Porto Alegre, RS, Brasil. [email protected], [email protected], [email protected] ABSTRACT – In this paper, we describe new postcranial remains of Chiniquodon cf. C. theotonicus, a chiniquodontid cynodont from the Therapsid Cenozone, from the Santa Maria Formation, Middle Triassic of Southern Brazil. In the described specimen are preserved almost all presacral vertebrae, the sacral vertebrae, an incomplete pelvic girdle, the left femur, and two metapodials. Some of these bones show slight differences relative to those already described for C. theotonicus, especially in the femur and in the pelvic girdle. Since the species can actually include the materials attributed to the genera Probelesodon (except from P. sanjuanensis) and Belesodon, however, these differences may represent normal ontogenetic variation in the species rather than being of taxonomically diagnostic value. Key words: Triassic, Santa Maria Formation, Brazil, Chiniquodontidae, Chiniquodon, postcranial skeleton. RESUMO – Neste trabalho são descritos novos elementos pós-cranianos de Chiniquodon cf. C. theotonicus, um cinodonte chiniquodontídeo da Cenozona de Therapsida, da Formação Santa Maria, Triássico Médio do sul do Brasil. No espécime descrito estão preservadas quase todas as vértebras pré-sacrais, as vértebras sacrais, a cintura pélvica incompleta, o fêmur esquerdo e dois metapodiais. Alguns destes ossos apresentam pequenas diferenças em relação àqueles previamente descri- tos para C. -
Redalyc.New Information on Riograndia Guaibensis Bonaparte
Anais da Academia Brasileira de Ciências ISSN: 0001-3765 [email protected] Academia Brasileira de Ciências Brasil SOARES, MARINA B.; SCHULTZ, CESAR L.; HORN, BRUNO L.D. New information on Riograndia guaibensis Bonaparte, Ferigolo & Ribeiro, 2001 (Eucynodontia, Tritheledontidae) from the Late Triassic of southern Brazil: anatomical and biostratigraphic implications Anais da Academia Brasileira de Ciências, vol. 83, núm. 1, marzo, 2011, pp. 329-354 Academia Brasileira de Ciências Rio de Janeiro, Brasil Available in: http://www.redalyc.org/articulo.oa?id=32717681018 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative “main” — 2011/2/12 — 13:39 — page 329 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 329-354 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc New information on Riograndia guaibensis Bonaparte, Ferigolo & Ribeiro, 2001 (Eucynodontia, Tritheledontidae) from the Late Triassic of southern Brazil: anatomical and biostratigraphic implications MARINA B. SOARES, CESAR L. SCHULTZ and BRUNO L.D. HORN Departamento de Paleontologia e Estratigrafia, Instituto de Geociências, Universidade Federal do Rio Grande doSul Av. Bento Gonçalves, 9500, Caixa Postal 15.001, 91501-970 Porto Alegre, RS, Brasil Manuscript received on December 20, 2010; accepted for publication on January 24, 2011 ABSTRACT The tritheledontid Riograndia guaibensis was the first cynodont described for the “Caturrita Formation” fauna from the Late Triassic of southern Brazil (Santa Maria 2 Sequence). -
DINOSAUR SUCCESS in the TRIASSIC: a NONCOMPETITIVE ECOLOGICAL MODEL This Content Downloaded from 137.222.248.217 on Sat, 17
VOLUME 58, No. 1 THE QUARTERLY REVIEW OF BIOLOGY MARCH 1983 DINOSAUR SUCCESS IN THE TRIASSIC: A NONCOMPETITIVE ECOLOGICAL MODEL MICHAEL J. BENTON University Museum, Parks Road, Oxford OX] 3PW, England, UK ABSTRACT The initial radiation of the dinosaurs in the Triassic period (about 200 million years ago) has been generally regarded as a result of successful competition with the previously dominant mammal- like reptiles. A detailed review of major terrestrial reptile faunas of the Permo- Triassic, including estimates of relative abundance, gives a different picture of the pattern of faunal replacements. Dinosaurs only appeared as dominant faunal elements in the latest Triassic after the disappear- ance of several groups qf mammal-like reptiles, thecondontians (ancestors of dinosaurs and other archosaurs), and rhynchosaurs (medium-sized herbivores). The concepts of differential survival ("competitive") and opportunistic ecological replacement of higher taxonomic categories are contrasted (the latter involves chance radiation to fill adaptive zones that are already empty), and they are applied to the fossil record. There is no evidence that either thecodontians or dinosaurs demonstrated their superiority over mammal-like reptiles in massive competitive take-overs. Thecodontians arose as medium-sized carnivores after the extinction of certain mammal-like reptiles (opportunism, latest Permian). Throughout most of the Triassic, the thecodontians shared carnivore adaptive zones with advanced mammal-like reptiles (cynodonts) until the latter became extinct (random processes, early to late Triassic). Among herbivores, the dicynodont mammal-like reptiles were largely replaced by diademodontoid mammal-like reptiles and rhynchosaurs (differential survival, middle to late Triassic). These groups then became extinct and dinosaurs replaced them and radiated rapidly (opportunism, latest Triassic).