New Mammals from the Marine Selandian of Maret, Belgium, and Their Implications for the Age of the Paleocene Continental Deposits of Walbeek, Germany

Total Page:16

File Type:pdf, Size:1020Kb

New Mammals from the Marine Selandian of Maret, Belgium, and Their Implications for the Age of the Paleocene Continental Deposits of Walbeek, Germany GEOLOGICA BELGICA (2013) 16/4: 236-244 New mammals from the marine Selandian of Maret, Belgium, and their implications for the age of the Paleocene continental deposits of Walbeek, Germany Eric DE BAST, Etienne STEURBAUT & Thierry SMITH O.D. Earth and History ofLife, Royal Belgian Institute for Natural Sciences, Rue lautier 29, 1000 Brussels, Belgium ABSTRACT. The early to middle Selandian fossiliferous Orp Sand Member of the Heers Fonnation in Belgium has regularly been excavated at its type-locality Maret for its rich and diversified selachian fauna. Among the abundant vertebrate remains, extremely rare mammal specimens have been found. Three isolated teeth have been published previously, all with uncertain affinities. The purpose of this study is to present new specimens from the same deposits, including a small well-preserved dentary of an adapisoriculid attributable to “Afrodon” germanicus, a fragmentary upper molar, referred to Berndestes sp., and a premolar of a large arctocyonid. Among the previous specimens we identified Arctocyonides cf. weigeld. The adapisoriculid dentary offers new clues that allow transferring “Afrodon’ germanicus to tile genus Bustylus. The five mammal taxa from Maret indicate an age intermediate between reference-levels MP1-5 of Hainin, Belgium and MP6 of Cemay, France and present the greatest correlation with the rich Walbeek fauna in Germany. The deposits from Walbeek were usually thought to be slightly older than the late Thanetian deposits of Cemay. We infer here that the age of Walbeek is likely to be Selandian. The strong differences observed between Hainin on the one hand, and Walbeek and Cemay on tile other hand, document a dispersal event from North America to Europe around the Danian-Selandian boundary. KEYWORDS: Orp Sand Member, Heers Formation, Biostratigraphy, Paleobiogeography, Adapisoriculidae 1. Introduction Herman & Sigé, 1975). Unfortunately, tile specimens figured by Herman and Sigé ( 1975 ) were not deposited in a public institution or even numbered, and seem to be lost. However, casts of tile Paleocene continental deposits of northwestern Europe are specimens were recovered in the collection of tile University of extremely discontinuous, both in space and time. This is essentially Montpellier; these casts are now deposited at tile RBINS with because a large part of Europe’s surface was flooded by shallow type and figured specimen numbers. These previously mentioned epicontinental seas and the remaining continental sedimentary specimens, together with tile new Orp Sand records, including archive was largely destroyed by the many subsequent vast marine an adapisoriculid jaw, are discussed here and compared to other transgressions (Vinken, 1988; Pomerol, 1989; Steurbaut, 1998). Paleocene mammal faunas of Europe. The stratigraphie position and age of these continental deposits are particularly difficult to establish, essentially because of the lack of suitable bio stratigraphie markers. This prevents easy and Institutional abbreviations— IRSNB, Royal Belgian Institute accurate correlation between the terrestrial and marine records of Natural Sciences, Brussels, Belgium; MLU Wa, Walbeek, and with the Geological Time Scale. The often short time span Institut für Geologische Wissenschaften und Geiseltalmuseum, covering many of the continental strata and the scarcity of well- Martin-Luther-Universität Halle-Wittenberg, Gennany. studied localities are not helping either. Palynomorphs provide one of the rare keys for disentangling the continental-marine 2. The Maret site and its spatial and temporal setting relationships (Steurbaut et al., 2003). Another key that helps in constraining the age estimates of continental faunas are remains The fossiliferous outcrops of Maret, a hamlet of the village Orp- of continental vertebrates found in marine deposits (Smitii & le-Grand, about halfway between tile towns of Leuven and Liège, Smith, 2003; Smith et al., 2004). have been intermittently but intensively investigated since the end of the 19,hcentury (see Herman & Sigé, 1975 for an overview). Among Paleocene MP levels (international mammal The mammal remains studied here have been collected on reference-levels for the European Paleogene, see Schmidt-Kittler, both sides of tile Maret railway track, and at different spots in 1987 and BiochroM’97, 1997), only MP6, which corresponds tile over 100 m wide exposure zones (coordinates 50°42’40”N, to the upper Thanetian, has been definitely identified based on 4°59’59”E). Herman & Sigé (1975) sampled on the North and tile mammal fauna from Cemay. The fauna of Hainin (Mons Basin, Belgium) is the only European fauna that is clearly older than the typical Cemaysian MP6 level. It is therefore the only representative for the interval M PI-5, which needs to be redefined and subdivided in the future when new intermediate mammal faunas are found. In his study on the Paleocene mammals of Europe, Russell (1964) noticed that many taxa of tile continental fauna of Walbeek (Germany) showed slightly more primitive features than similar taxa from Cemay. Walbeek ^?\M aret was later suggested to represent MP?5 (Schmidt-Kittler, 1987, BiochroM’97, 1997; Gheerbrant et al., 1999; Smith & Smitii, 2003), but tile aberrant mammal assemblage coupled with the lack of stratigraphie control prevented scientists from considering BELGIUM Walbeek as a reference-level (Schmidt-Kittler, 1987). New fossil terrestrial mammal specimens have recently FRANCE been collected from tile Orp Sand Member at Maret, the type- locality of this stratigraphie unit (Steurbaut, 1998) (Fig. 1). At this particular site, these Mid-Paleocene sands are renowned for c. 60.0 Ma - Selandian their rich marine selachian fauna, and they represent tile locus | . Heers Formation typicus and stratum typicum of one genus and several species of E = erosion, influx Cretaceous coccoliths sharks (Herman, 1973, 1977; Cappetta & Nolf, 2005). Extremely E.S., 2008 ---------- isopachs (equidistance 20m) rare terrestrial vertebrate remains have been found in association with the marine vertebrates (Dollo, 1890; Herman, 1973), Figure 1.Current distribution of the Heers Formation in Belgium with among which are a few mammal specimens (Quinet et al., 1971; thickness estimates and location of the fossiliferous site of Maret. S e l a n d ia n m a m m a l s f r o m B e l g iu m 237 At Maret, the Orp Sands, of which only the upper 4 m are The Maret outcrop section in Central Belgiumexposed, consist of a heterogeneous complex of essentially sandy sediments, with intermittent influxes of whitish marl m material, sometimes forming thin beds, but mostly restricted to * I * I * i centimetric to decimetric large irregular marl lumps (Fig. 2). The 1*1* i * at high carbonate content of these marls is due to the presence of blocky siliceous whitish i= reworked Cretaceous coccoliths (Fig. 1). Sedimentation took 1*1 * * I limestone, glauconitic o H O STT jT-r ^ r i H t/> place in a shallow marine context, with temporary estuarine 0 influences, at the edge of the continent, with exposed chalk strata *1*1*1 * I * ) E 25 (cliffs? Bless & Fernández-Narvaiza, 1996, fig. 36; Dreesen et highly glauconitic * • . il al., 1998). This is evidenced by the presence of bioturbated and c T O 0 horizontally stratified sands and thin marl beds, pointing to rather more sandy O towards the base c calm sedimentation conditions, and the reworked marl lumps, the -a-b-C gravel bed concentrations of glauconite and the channeling, reflecting high- _ . V I ~S energy input. u i i I g IO TT7 grey marly stonebed GM The three other isolated mammal teeth from Maret were encountered in the basal gravel of the Lincent Limestone Member. fine stratified sand This siliceous limestone to calcareous sandstone unit, overlying a thin basal gravel, represents the lower Member of the Hamiut Formation. In agreement with its attribution to the lower part of biotubated clayey sand with 4 - nannofossil zone NP8, it belongs to the lower middle Thanetian. //. & large marl chunks O The basal gravel layer in Maret has yielded a rich selachian fauna. Or7* ? , 0 -Q In between the Orp Sand Member and the Lincent Member intercalation of stratified E occurs a whitish crumbly marly chalk, the Gelinden Marl Member, sand and marl layers 0 i ^ i y i ^ i ^ i et the thickness of which is reduced to less than 1 m at Maret. The age o estimate of the Gelinden Marl Member is mid to late Selandian several sets of glauconitic“D LL C on the basis of the calcareous nannofossil (upper NP4-NP5) and sand 0 co dinoflagellate associations (Zone 3 of Heihnann-Clausen (1985), co Qt Q_ recorded in the upper part of the Æbelo Fonnation and base of the S bioturbated clayey sand LU LU Holmehus Formation in Denmark (Sheldon et al., 2012). biotubated clayey sand X with large marl chunks 3. Systematic Palaeontology bioturbated clayey sand Class Mammalia Linnaeus, 1758 GM = Gelinden Marl Member ES Grandorder Euarchonta? Waddell, Okada, and Hasegawa, 1999 M = location of mammal specimens 2013 Family Adapisoriculidae Van Valen, 1967 Genus Bustylus Gheerbrant & Russell, 1991 Figure 2. Lithology and lithostratigraphic interpretation of the Maret Type species: Bnstyliis cemaysi Gheerbrant & Russell, 1991 outcrop (logged on the southern side of the railtrack on June 16th 1992), with location of the mammal finds: a. Herman, 1973 and Herman & Sigé, Bustylus germanicus (Russell, 1964) comb. nov. 1974; b. Quinet et al., 1971; c. this paper. (Fig. 3C) Referred specimens: IRSNB M2017, left dentary with p3-m3 South sides of the track, all others (Quinet et al., 1971; this paper) in place, from the Orp Sand Member of the Heers Fonnation at only on the South side (see Herman & Sigé, 1975 for a detailed Maret. map of tile area). This southern site, last re-excavated in the early 1990s, was logged in 1992 (Fig. 2). Measurements: p4: L = 1,41 nun, 1 = 0,67 nun; ml: L = 1,35 nun, Of tile six mammal specimens discussed here, three 1 = 0,74 nun; m2: L = 1,31 nun, 1 = 0,75 nun; m3: L = 1,27 nun, come from the Orp Sand Member, which at Maret, as nearly 1 = 0,70 mm.
Recommended publications
  • The World at the Time of Messel: Conference Volume
    T. Lehmann & S.F.K. Schaal (eds) The World at the Time of Messel - Conference Volume Time at the The World The World at the Time of Messel: Puzzles in Palaeobiology, Palaeoenvironment and the History of Early Primates 22nd International Senckenberg Conference 2011 Frankfurt am Main, 15th - 19th November 2011 ISBN 978-3-929907-86-5 Conference Volume SENCKENBERG Gesellschaft für Naturforschung THOMAS LEHMANN & STEPHAN F.K. SCHAAL (eds) The World at the Time of Messel: Puzzles in Palaeobiology, Palaeoenvironment, and the History of Early Primates 22nd International Senckenberg Conference Frankfurt am Main, 15th – 19th November 2011 Conference Volume Senckenberg Gesellschaft für Naturforschung IMPRINT The World at the Time of Messel: Puzzles in Palaeobiology, Palaeoenvironment, and the History of Early Primates 22nd International Senckenberg Conference 15th – 19th November 2011, Frankfurt am Main, Germany Conference Volume Publisher PROF. DR. DR. H.C. VOLKER MOSBRUGGER Senckenberg Gesellschaft für Naturforschung Senckenberganlage 25, 60325 Frankfurt am Main, Germany Editors DR. THOMAS LEHMANN & DR. STEPHAN F.K. SCHAAL Senckenberg Research Institute and Natural History Museum Frankfurt Senckenberganlage 25, 60325 Frankfurt am Main, Germany [email protected]; [email protected] Language editors JOSEPH E.B. HOGAN & DR. KRISTER T. SMITH Layout JULIANE EBERHARDT & ANIKA VOGEL Cover Illustration EVELINE JUNQUEIRA Print Rhein-Main-Geschäftsdrucke, Hofheim-Wallau, Germany Citation LEHMANN, T. & SCHAAL, S.F.K. (eds) (2011). The World at the Time of Messel: Puzzles in Palaeobiology, Palaeoenvironment, and the History of Early Primates. 22nd International Senckenberg Conference. 15th – 19th November 2011, Frankfurt am Main. Conference Volume. Senckenberg Gesellschaft für Naturforschung, Frankfurt am Main. pp. 203.
    [Show full text]
  • Historical Biogeography of the Late Cretaceous Vertebrates of India: Comparison of Geophysical and Paleontological Data
    Khosla, A. and Lucas, S.G., eds., 2016, Cretaceous Period: Biotic Diversity and Biogeography. New Mexico Museum of Natural History and Science Bulletin 71. 317 HISTORICAL BIOGEOGRAPHY OF THE LATE CRETACEOUS VERTEBRATES OF INDIA: COMPARISON OF GEOPHYSICAL AND PALEONTOLOGICAL DATA OMKAR VERMA1, ASHU KHOSLA2, FRANCISCO J. GOIN3 AND JASDEEP KAUR2 1Geology Discipline Group, School of Sciences, Indira Gandhi National Open University, New Delhi – 110 068, India, e-mail: omkarverma@ ignou.ac.in; 2Department of Geology, Centre for Advanced Studies, Panjab University, Sector-14, Chandigarh – 160014, India, e-mail: [email protected], e-mail: [email protected]; 3Consejo Nacional de Investigaciones Científicas y Técnicas and División Paleontología Vertebrados, Museo de Ciencias Naturales de La Plata, B1900FWA La Plata, Argentina, e-mail: [email protected] Abstract—The Cretaceous was a special time for the Indian plate as it was separated from Gondwana landmasses and started its northward journey across the Tethys Sea towards the Equator. The northward movement of this plate implied shifting latitudes and climate belts, until it finally collided with Asia during the early Cenozoic. Geophysical data and plate tectonic models show that after splitting from Gondwana, the Indian plate remained as an isolated continent for more than 45 Ma during the Cretaceous; thus, it predicts a remarkable biotic endemism for the continent. Paleontological data on the Cretaceous vertebrates of India is best known for Maastrichtian time; in turn, the pre-Maastrichtian record is very poor—it contains very few fossils of fishes and marine reptiles. The Maastrichtian fossil record comprises vertebrates of Gondwana and Laurasian affinities and some endemic, ancient lineages as well.
    [Show full text]
  • Divergence Time Estimates of Mammals from Molecular Clocks and Fossils 649
    Divergence time estimates of mammals from molecular clocks and fossils 649 Divergence time estimates of mammals from molecular clocks and fossils: Relevance of new fossil fi nds from India G V R PRASAD Indian Institute of Science Education and Research (IISER-K), BCKV Main Campus, Mohanpur 741 252, India (Email, [email protected]) This paper presents a brief review of recent advances in the classifi cation of mammals at higher levels using fossils and molecular clocks. It also discusses latest fossil discoveries from the Cretaceous – Eocene (66–55 m.y.) rocks of India and their relevance to our current understanding of placental mammal origins and diversifi cations. [Prasad G V R 2009 Divergence time estimates of mammals from molecular clocks and fossils: Relevance of new fossil fi nds from India; J. Biosci. 34 649–659] DOI 10.1007/s12038-009-0063-x 1. Introduction (Scandentia, Primates, Chiroptera, and Dermoptera), (5) Volitantia (Chiroptera and Dermoptera), (6) Cetungulata In order to understand the rates of evolution and patterns (Artiodactyla, Cetacea, Perissodactyla, Hyracoidea, in biogeography, precise estimation of divergence time of Proboscidea, Sirenia), (7) Paenungulata (Hyracoidea, major taxonomic groups is very important. Traditionally Proboscidea, Sirenia), and (8) Tethytheria (Proboscidea and species divergence time estimates were made using the Sirenia) was suggested for placental mammals based on time of fi rst appearance of new species in the fossil record. morphology of fossils (Shoshani and McKenna 1998). However, there is always a time lag between the time of In the last decade and a half, mammalian phylogeny and actual divergence and the fi rst appearance in the fossil lineage divergence dates underwent very rapid transfor- record as morphological distinction between two species is mation with the extensive use of molecular clock methods.
    [Show full text]
  • A Radiation of Arboreal Basal Eutherian Mammals Beginning in the Late Cretaceous of India
    A radiation of arboreal basal eutherian mammals beginning in the Late Cretaceous of India Anjali Goswamia,b,1, Guntupalli V. R. Prasadc, Paul Upchurchb, Doug M. Boyerd, Erik R. Seifferte, Omkar Vermaf, Emmanuel Gheerbrantg, and John J. Flynnh aDepartment of Genetics, Evolution, and Environment, bDepartment of Earth Sciences, University College London, London WC1E 6BT, United Kingdom; cDepartment of Geology, Centre for Advanced Studies, University of Delhi, Delhi 110 007, India; dDepartment of Anthropology and Archaeology, Brooklyn College, City University of New York, Brooklyn, NY 11210; eDepartment of Anatomical Sciences, Stony Brook University, Stony Brook, NY 11794-8081; fSchool of Sciences, Indira Gandhi National Open University, New Delhi 110 068, India; gUnité Mixte de Recherche 7207 du Centre National de la Recherche Scientifique (CR2P), Département Histoire de la Terre, Muséum National d’Histoire Naturelle, 75005 Paris, France; and hDivision of Paleontology and Richard Gilder Graduate School, American Museum of Natural History, New York, NY 10024 Edited* by Elwyn L. Simons, Duke University, Durham, NC, and approved August 15, 2011 (received for review June 6, 2011) India’s Late Cretaceous fossil mammals include the only undis- cluding placentals and their stem relatives) are known from the puted pre-Tertiary Gondwanan eutherians, such as Deccanolestes. Late Cretaceous of Laurasia (North America, Europe, and Asia) Recent studies have suggested a relationship between Deccano- (9), and although a few have been suggested as possible pla- lestes and African and European Paleocene adapisoriculids, which centals [e.g., Protungulatum (10)], none are unequivocally sup- have been variably identified as stem euarchontans, stem pri- ported as a Cretaceous placental mammal (2).
    [Show full text]
  • Evolution and Paleoenvironment of Early Modern Vertebrates During the Paleogene Program and Abstracts
    September 10‐13, 2019 Royal Belgian Institute of natural Sciences, Brussels, Belgium International symposium Evolution and Paleoenvironment of Early Modern Vertebrates during the Paleogene Program and abstracts PalEurAfrica Meeting 2019 In the framework of the PalEurAfrica research project (see http://www.paleurafrica.be), we are happy to invite you to the Royal Belgian Institute of Natural Sciences (RBINS) for an international symposium related to the evolution and paleoenvironment of early modern vertebrates during the Paleogene. This allows us to gather specialists who work on macro‐ and micropaleontology, bio‐ and isotope stratigraphy, paleoenvironment, paleogeography, and geology of Paleogene vertebrate bearing sites. This international meeting also celebrates the memory of one of our PalEurAfrica partners, Gregg Gunnell (1954‐2017), who tragically died unexpectedly in the middle of his career, having made significant contributions to our understanding of research on Paleogene vertebrate evolutionary history. Host committee Thierry Smith (Chair) – Royal Belgian Institute of Natural Sciences, Brussels, Belgium Thierry De Putter – Royal Museum for Central Africa, Tervuren, Belgium Stephen Louwye – Universiteit Gent, Gent, Belgium Johan Yans – Université de Namur, Namur, Belgium Matthew Borths – Duke University Lemur center, Durham, NC, USA Nancy Stevens – Ohio University, Athens, OH, USA Scientific committee Massimo Delfino – Università di Torino, Torino, Italy Gilles Escarguel – Université de Lyon, Lyon, France Annelise Folie – Royal Belgian Institute of Natural Sciences, Brussels, Belgium Emmanuel Gheerbrant – Museum national d’Histoire Naturelle, Paris, France Jason Head – University of Cambridge, Cambridge, UK Gerald Mayr – Senckenberg Forschungsinstitut und Naturmuseum, Frankfurt, Germany Florias Mees – Royal Museum for Central Africa, Tervuren, Belgium Ellen R. Miller – Wake Forest University, Winston‐Salem, NC, USA Adán Pérez‐García – Universidad Nacional de Educación a Distancia, Madrid, Spain Rajendra Singh Rana – H.N.B.
    [Show full text]
  • Vertebrate Evolution on the Indian Raft - Biogeographic Conundrums
    Article 461 by Varun Parmar1, and G.V.R. Prasad2* Vertebrate evolution on the Indian raft - Biogeographic conundrums 1Department of Geology, University of Jammu, Jammu – 180006, India; E-mail: [email protected] 2Department of Geology, Centre for Advanced Studies, University of Delhi, Delhi – 110007, India; *Corresponding author, E-mail: [email protected] (Received : 9/09/2019; Revised accepted : 28/10/2019) https://doi.org/10.18814/epiiugs/2020/020029 The Indian plate has a long history of rifting, drifting the palaeogeographic reconstructions, the supercontinent Pangea and collision. It travelled for about 9000 km from its remained intact until the Late Jurassic, whereafter it started to break apart into the northern landmass of Laurasia and the southern landmass position within Gondwana to reach its present position of Gondwana. This separation was slow, such that only a narrow within Asia. During its northward journey, the Indian seaway opened up between Laurasia and Gondwana. Towards the landmass remained physically isolated for about 35 Ma end of the Jurassic (~167 Ma) fragmentation of Gondwana into East from all other landmasses after its final break-up from and West Gondwana occurred (Lawver et al., 1991). East Gondwana Madagascar. A critical examination of the vertebrate comprised landmasses such as India, Madagascar, Antarctica, and Australia whereas West Gondwana consisted of Africa and South fossil record of the Indian plate for the period of early America (Lawver et al., 1991). Later in the Early Cretaceous (~130 and late drift phases offers very limited information for Ma), the Indo-Madagascar-Seychelles block was separated from the the early drift phase, but reveals a complex Antarctica-Australia block.
    [Show full text]
  • Widanelfarasia, a Diminutive Placental from the Late Eocene of Egypt
    Widanelfarasia, a diminutive placental from the late Eocene of Egypt Erik R. Seiffert* and Elwyn L. Simons*†‡ *Department of Biological Anthropology and Anatomy, Duke University, Box 90383, Durham, NC 27708-0383; and †Primate Center, Duke University, 3705 Erwin Road, Durham, NC 27705 Contributed by Elwyn L. Simons, December 15, 1999 The lower dentition of Widanelfarasia (new genus), a diminutive Cimolestes, Aboletylestes, indeterminate didelphodontines) as late Eocene placental from the Fayum Depression in Egypt, is well as a possible endemic form referred to Proteutheria, described. Widanelfarasia exhibits a complex of features associ- Todralestes, have also been described from the Ouarzazate Basin ated with incipient zalambdodonty and at least three unequivocal (5, 7, 8). apomorphies [loss of P1, an enlarged I2 (relative to I3), and a basal These diminutive north African eutherians have provided new cusp on I2], which provide weak support for its placement as a evidence for the presence of intermittent biogeographical con- possible sister taxon of either a tenrecid–chrysochlorid clade or of nections between Afro-Arabia and Laurasia during the early solenodontids. The former hypothesis gains additional support Cenozoic (16) and have helped to elucidate a considerable from biogeographical evidence, but both scenarios are currently degree of biogeographical cosmopolitanism for palaeoryctoids tenuous as Widanelfarasia is clearly not truly zalambdodont. through the late Cretaceous and early Paleogene (e.g., ref. 17). Phylogenetic hypotheses positing affinities with tenrecids alone or Due to the limited nature of the available material, however, it chrysochlorids alone must invoke either convergent acquisition of remains unclear just how the scarce Eocene Afro-Arabian zalambdodonty in these taxa or autapomorphic reversal in ‘‘lipotyphlans’’ may relate to living and extinct Laurasian forms Widanelfarasia.
    [Show full text]
  • Diversity of the Adapisoriculid Mammals from the Early Palaeocene of Hainin, Belgium
    Diversity of the adapisoriculid mammals from the early Palaeocene of Hainin, Belgium ERIC DE BAST, BERNARD SIGÉ, and THIERRY SMITH De Bast, E., Smith, T. and Sigé, B. 2012. Diversity of the adapisoriculid mammals from the early Palaeocene of Hainin, Belgium. Acta Palaeontologica Polonica 57 (1): 35–52. Adapisoriculidae are an enigmatic group of small mammals known from the late Cretaceous of India, and from the early Palaeocene to early Eocene of Europe and Africa. Based on their primitive dental morphology, they have been classified as didelphids, nyctitheriids, leptictids, mixodectids, tupaiids, and palaeoryctids. While the latest hypothesis based on den− tal morphology suggests an affinity with Lipotyphla, postcranial remains indicate a close relationship with Euarchonta. Here, we present new adapisoriculid dental remains from the early Palaeocene locality of Hainin (Belgium). Adapiso− riculidae are particularly abundant in Hainin, where they represent about one third of the mammalian fauna, offering new insights into both their specific and generic phylogenetic interrelationships. We describe three new species (Afrodon gheerbranti sp. nov., Bustylus folieae sp. nov. and Proremiculus lagnauxi gen. et sp. nov.) and document the previously unknown lower dentition of Bustylus marandati. The diversity of dental morphologies observed in the Hainin fauna sug− gests different interrelationships than previously suggested. In particular, the genus Proremiculus is considered morpho− logically intermediate between Afrodon and Remiculus, and the latter is no longer recognised as the sister group of Adapisoriculus. Although the highest diversity of adapisoriculids occurs in Europe, the oldest and most primitive mem− bers of the family were found in India and Africa, respectively. The geographic origin of the family could thus be located in any of these three continents, depending on the importance attributed to each of these factors.
    [Show full text]
  • Paleobiologie Et Des Mammiferes Evolution Du
    PALEOBIOLOGIE ET EVOLUTION DES MAMMIFERES DU PALEOGENE Volume jubilaire en hommage à Donald E. RUSSELL Avant-propos Contributions historiques Marc GODINOT & Philip D. GINGERICH Introduction à l'oeuvre scientifique de Donald E. Russell, "gentleman· paleontologist". .. 63 Bibliographie de Donald E. Russell. 75 Pierre LOUIS Recherches de mammifères paléogènes dans les départements de l'Aisne et de la Marne pendant la deuxième moitié du vingtième siècle. 83 Biostratigraphie et vitesses d'évolution Richard SMITH & Jeremy J. HOOKER Sur la présence de dents de mammifères (Creodonta, Perissodactyla) près de la limite Paléocène-Eocène à Hoegaarden, Belgique. 115 Suyin TING, Judith A. SCHIEBOUT & Jinjian ZHENG New records of the pantodont Archaeolambda from the Paleocene of southern China. 125 Spencer G. LUCAS Fossil mammals and the age of the Changxindian Formation, northeastern China. 133 Elena G. KORDIKOV A & Alexander V. MA VRIN Stratigraphy and Oligocene-Miocene mammalian biochronology of the Aktau Mountains, Dzhungarian Alatau Range, Kazakhstan. 141 Patricia A. HOLROYD, Elwyn L. SIMONS, Thomas M. BOWN, Paul D. POLLY & Mary J. KRAUS New records of terres trial mammals from the Upper Eocene Qasr El Sagha Formation, Fayum Depression, Egypt. 175 Philip D. GINGERICH Rates of evolution in divergent species lineages as a test of character displacement in the fossil record: tooth size in Paleocene Plesiadapis (Mammalia, Proprimates) . 193 59 Etudes fonctionnelles, paléobiologie et paléoenvironnements Percy M. BUTLER Dilambdodont molars: a functional interpretation of their evolution . .. 205 Gerhard STORCH Paleobiology of MesseI erinaceomorphs.......................................... 215 Marc GODINOT, Thierry SMITH & Richard SMITH Mode de vie et affinités de Paschatherium (Condylarthra, Hyopsodontidae) d'après ses os du tarse .
    [Show full text]
  • [Italic Page Numbers Indicate Major References] Aaron's Locality, Alberta, 59 Acarictis Ryani, 157 Achaenodon Sp., 214 Acheronod
    Index [Italic page numbers indicate major references] Aaron's locality, Alberta, 59 Arfia, 118, 180 Biohorizon C, 144 Acarictis ryani, 157 sp., 88 Biomphalaria, 178 Achaenodon sp., 214 Arminto, 170, 179 biostratigraphic zonation, 2 Acheronodon, 59 Armintodelphys Bisonalveus, 61, 62, 87 acritarchs, 16 blacki, 177, 183 browni, 59 Adapidae, 88, 89, 91, 93, 94, 95, 96, dawsoni 177 sp., 60, 67 194 Artiodactyla, 74, 89, 91, 93, 94, 95, Black Butte, 45 Adrar Mgorn locality, 89, 93 96, 108, 129 Blackfalds, Alberta, 60 Africa, 72,74, 89, 91 Asia, 74 , 88, 93 Blindman River, 52, 58, 60, 62 Afrodon chleuhi, 94 Asiocoryphodon, 88 blue clay horizon, 175 Alberta, 2, 11, 16, 32, 52, 53, 56, assemblages Bobcat Draw, 140 57,58,59, 60, 61,62 , 65, 66, Buck Spring, 180,182 Bobcat Member, 16 67, 83 Elderberry Canyon, 207 bones Alberta Syncline, 52 lizard, 180 fossil, 188 Alberta Well, 56 microfossil, 9 fragments, 172 Allognath osuchus, 180 quarry, 180 Bow River, 52, 57, 58 alluvial fans, 170, 189 Tepee Trail, 208 braidplains, 170 alluvial paleosols, 135,149, 172 avulsion, 179 Bridger Formation, 108, 207 Alocodontulum, 108, 109, 114, 130 Brontotheriidae, 96 atopum, 109, 114 Baculites Bubogonia saskia, 55 Alphadon, 39, 40, 43, 44 asperiformis zone, 14, 18 Buck Spring Quarries, 169, 170, 172, sp., 45, 54, 55 clinolobatus zone, 11, 18 178 Alveojunctus, 180 gregoryensis zone, 4 B sequence, 174 Amia, 54, 56, 59, 63, 180 obtusus zone, 11 B-l horizon, 175 uintensis, 182 reduncus zone, 4 B-2 horizon, 169,175,176, 179, amphibians, 182 reesidei zone, 11 180,182 Amphidozotherium, 216 scotti zone, 4 blue clay horizon, 175 Amynodon advenus, 214 sp.
    [Show full text]
  • New Postcranial Bones of the Extinct Mammalian Family Nyctitheriidae (Paleogene, UK): Primitive Euarchontans with Scansorial Locomotion
    Palaeontologia Electronica palaeo-electronica.org New postcranial bones of the extinct mammalian family Nyctitheriidae (Paleogene, UK): Primitive euarchontans with scansorial locomotion Jerry J. Hooker ABSTRACT New postcranial bones from the Late Eocene and earliest Oligocene of the Hamp- shire Basin, UK, are identified as belonging to the extinct family Nyctitheriidae. Previ- ously, astragali and calcanea were the only elements apart from teeth and jaws to be unequivocally recognized. Now, humeri, radii, a metacarpal, femora, distal tibiae, naviculars, cuboids, an ectocuneiform, metatarsals and phalanges, together with addi- tional astragali and calcanea, have been collected. These are shown to belong to a diversity of nyctithere taxa previously named from dental remains. Functional analysis shows that nyctitheres had mobile shoulder and hip joints, could pronate and supinate the radius, partially invert the foot at the astragalocalcaneal and upper ankle joints using powerful flexor muscles, all indicative of a scansorial lifestyle and allowing head- first descent on vertical surfaces. Climbing appears to have been dominated by flexion of the forearms and feet. Cladistic analysis employing a range of primitive eutherian mammals shows that nyctitheres are stem euarchontans, rather than lipotyphlans, with which they had previously been classified based on dental characters. Earlier ideas of relationships with the extinct Adapisoriculidae, recently considered stem eutherians, are not upheld. Jerry J. Hooker. Department of Earth Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK. [email protected] Keywords: Eutheria; Lipotyphla; placental; Scandentia; shrews; Soricidae INTRODUCTION basis of some straight slender limb bone shafts, apparently associated with teeth (on which this Nyctitherium Marsh, 1872, the type genus of genus was based), returned to Marsh’s original the eutherian family Nyctitheriidae Simpson, 1928a idea that Nyctitherium was a chiropteran.
    [Show full text]
  • A Radiation of Arboreal Basal Eutherian Mammals Beginning in the Late Cretaceous of India
    A radiation of arboreal basal eutherian mammals beginning in the Late Cretaceous of India Anjali Goswamia,b,1, Guntupalli V. R. Prasadc, Paul Upchurchb, Doug M. Boyerd, Erik R. Seifferte, Omkar Vermaf, Emmanuel Gheerbrantg, and John J. Flynnh aDepartment of Genetics, Evolution, and Environment, bDepartment of Earth Sciences, University College London, London WC1E 6BT, United Kingdom; cDepartment of Geology, Centre for Advanced Studies, University of Delhi, Delhi 110 007, India; dDepartment of Anthropology and Archaeology, Brooklyn College, City University of New York, Brooklyn, NY 11210; eDepartment of Anatomical Sciences, Stony Brook University, Stony Brook, NY 11794-8081; fSchool of Sciences, Indira Gandhi National Open University, New Delhi 110 068, India; gUnité Mixte de Recherche 7207 du Centre National de la Recherche Scientifique (CR2P), Département Histoire de la Terre, Muséum National d’Histoire Naturelle, 75005 Paris, France; and hDivision of Paleontology and Richard Gilder Graduate School, American Museum of Natural History, New York, NY 10024 Edited* by Elwyn L. Simons, Duke University, Durham, NC, and approved August 15, 2011 (received for review June 6, 2011) India’s Late Cretaceous fossil mammals include the only undis- cluding placentals and their stem relatives) are known from the puted pre-Tertiary Gondwanan eutherians, such as Deccanolestes. Late Cretaceous of Laurasia (North America, Europe, and Asia) Recent studies have suggested a relationship between Deccano- (9), and although a few have been suggested as possible pla- lestes and African and European Paleocene adapisoriculids, which centals [e.g., Protungulatum (10)], none are unequivocally sup- have been variably identified as stem euarchontans, stem pri- ported as a Cretaceous placental mammal (2).
    [Show full text]