The Evolution of Metapodial Bones in the Cave Bear Group And

Total Page:16

File Type:pdf, Size:1020Kb

The Evolution of Metapodial Bones in the Cave Bear Group And View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Repositorio da Universidade da Coruña Cadernos Lab. Xeolóxico de Laxe ISSN: 0213-4497 Coruña. 2001. Vol. 26, pp. 365-371 The Evolution of Metapodial Bones in the Cave Bear Group and its biostratigraphical Implications La evolución de los metápodos en el grupo del Oso de las Cavernas y sus implicaciones bioestratigráficas WITHALM, G. AB S T R A C T A short description of the methods is followed by some central results obtained from the analyses of metapodial bones in the cave bear group from sites in Austria and Italy. The evolution of metapodials shows, in general, a tendency towards increasing plumpness, and backs the results obtained from the morphodynamic analyses of the teeth. Key words: evolution, metapodials, Ursus spelaeus, Ursus deningeri Institute of Paleontology, University of Vienna, Althanstraße 14, A-1090, Vienna, AUSTRIA 366 WITHALM, G. CAD. LAB. XEOL. LAXE 26 (2001) INTRODUCTION Since the work done by TORRES (1988) and KUNST (1989) there was not too much attention drawn to the metapo- dial bones of Ursus spelaeus and its prede- cessor, Ursus deningeri. Torres tried to provide a range of cha- racters to differentiate U. spelaeus from U. deningeri and U. arctos as well as a general description and comparison of the skeletal elements of these animals, collected in sites from Spain. Kunst tried to use the metapodial bones to exemplify differences between several cave bear sites of Austria. RESULTS The current investigation is aimed at the evolutionary changes of the metapo- Figure 1. Measurements taken from metapo- dial bones throughout time by means of dials. Graphics: from TORRES (1988), altered. morphometrics. Therefore eight different measurements were taken and five indices were calculated from 4459 metapodial bones from U. spelaeus and U. deningeri Herdengel cave, Windener Bärenhöhle from eight different sites in Austria and and Gamssulzen cave. Italy. Basic statistical analysis was carried The measurements are: proximal out on this data set to see wether there is width and depth, smallest diaphyseal a possibility to sex a population or not, for width and depth, distal width and depth, comparison with the results from distal epicondyleal width and greatest OSWALD (1999). The obtained results length. The indices are: proximal area, are totally inhomogenous and so it is not smallest diaphyseal area, distal area, index possible to sex a cave bear fauna by means of robustness and K–index, the latter of metapodials. Further investigation sho- according to GUZVICA & RADANO- wed that there is a correlation between the VIC–GUZVICA (2000). index of robustness, the K–Index and the The sites from Austria and Italy are: smallest diaphyseal area and the stratigra- Hundsheimer Spalte, Repolust cave, phic position of the site. Therefore it is Schwabenreith cave, Ramesch cave, not only possible to predict the age of a Conturines cave (Southern Ty r o l ) , cave bear population by analysing the evo- CAD. LAB. XEOL. LAXE 26 (2001) The evolution of metapodial bones 367 Figure 2. Map showing the distribution of the sites in Austria and Italy. lutionary level of the teeth, but also by the cave bears. At first this material was divi- analysis of the metapodial bones. ded into two parts corresponding to the Special attention was drawn to the strata and the result was astonishing. In analysis of the material from Ramesch contradiction to the results obtained from cave (Upper Austria), because of the long the other sites, that is a trend towards period of time this cave was inhabited by plumper metapodial bones with a gro- Figure 3. Development of metacarpus (left) and metatarsus (right). Please note the astonishing dif- ference between the populations from Hundsheimer Spalte and Repolust cave as well as the decli- ne towards Conturines cave. Abbreviations: HH- Hundsheimer Spalte, RE- Repolust cave, SW- Schwabenreith cave, CU- Conturines cave (Southern Tyrol, Italy), HD- Herdengel cave, RK- Ramesch cave, WI- Windener Barenhöehle, GS- Gamssulzen cave. 368 WITHALM, G. CAD. LAB. XEOL. LAXE 26 (2001) wing smallest diaphyseal area, there was a of the bears from Conturines cave, follo- decline in the mean of the evolutionary wed by those from Herdengel cave in level in the upper part of the profile for Lower Austria. Despite their age these most of the metapodial bones. This decli- bears are plumper than one would expect. ne in dimensions is a phenomenon, which The high position of the Herdengel cave is was discovered first by RABEDER (pers. an artefact, which is based upon the pre- comm.) when he analysed the evolution of dominance of young bears in the profile, the teeth from the profile of the Ramesch i.e. there are much more metapodial bones cave in relation to the strata. Now it beco- from the upper parts of the profile and the mes more and more evident, that this problem that there are not enough meta- trend is not only visible in the evolution of podial bones to split the material. Here it the teeth, but also in the evolution of is clearly visible that plumpness is the hands and feet of this cave bear popula- speciality of the Conturines bear whereas tion. We assume that the reason therefore the dimensions show a significant decline. is a climatic change towards colder condi- Figure 5 shows that there is neither an tions. This reversion of the normal trend obvious nor a hidden correlation between towards bigger and plumper bears implies average of the index of plumpness and the some problems, especially for the predic- altitude of the site, what could have been tion of geological age. But it seems not to a plausible assumption as well. be a general trend even if there seems to be Another interesting fact is the big dif- a similar trend in the profile of the ference between the bears from the Herdengel cave but this can be due to a Hundsheimer Spalte (Lower Austria) and lack of material. those of the Repolust cave in Styria. For In figure 4, left diagram, there is a very stratigraphic and skeletal features the interesting peak representing the position bears from the Hundsheimer Spalte are Figure 4. The left diagram shows the development of the overall index of plumpness. The right diagram shows the development of the smallest diaphyseal area. Abbreviations: HH- Hundsheimer Spalte, RE- Repolust cave, SW- Schwabenreith cave, CU- Conturines cave (Southern Tyrol, Italy), HD- Herdengel cave, RK- Ramesch cave, WI- Windener Barenhöehle, GS- Gamssulzen cave. CAD. LAB. XEOL. LAXE 26 (2001) The evolution of metapodial bones 369 Figure 5. Index of plumpness versus altitude of site, left and index of plumpness and sex, right. This diagram shows that there is obviously no correlation between the mean index of plumpness of a cave- or deninger bear population and the altitude of the site. There is no correlation betwe- en the index of plumpness and sex too. known as U. deningeri, but they do have to the species U. deningeri it should be nearly spelaeoid dimensions, and, in some used for the same purpose. But now it will cases, they become even bigger than nor- be Ursus deningeri "deningeroides" mal cave bears do. The dimensions of the Furthermore, a really tiny metatarsal 5 bears from the Hundsheimer Spalte differ was found in the material of the from the deninger-bears from Hundsheimer Spalte, which fits perfectly Repolusthöhle (Styria) in a range from 6 well into the range of robustness of Ursus % until 16,6 % ! These differences could arctos. But it is not only the plumpness, be sufficient to define a new species. The which is responsible for the difference to really small deninger bears from the those of the cave bear, it is also the mor- Repolust cave are so different, that it phology, showing all the features of a seems to be more correct to separate this modern brown bear. In respect to the age form the other deninger bears on the subs- of this site the metapodial in question is pecies level. I would like to suggest the described as Ursus cf. arctos, which is new usage of the old terminus "deningeroides", to the faunal list of this site as well as for which was introduced into literature by the Lower Pleistocene. Maria MOTTL (1947). She used this term Another very interesting cave is the to mark the peculiarities of this bear from Windener Baerenhöhle. There were two which she believed that it was a cave bear. different species of bears found: a big cave Now that it is clear that this bear belongs bear and a very big brown bear. These 370 WITHALM, G. CAD. LAB. XEOL. LAXE 26 (2001) bears do not differ in greatest length of the plumpness. We should take into account metapodial bones but in robustness and in the smaller dimensions of these animals in some morphological details of the diaphy- addition to their dental status and we have sis. The brown bear was determined by a combination that makes this bear uni- THENIUS (1956) and its name is U. arc - que. There is no doubt, that further inves- tos priscus. It inhabited this cave about 17 tigation in the Conturines bear will bring ky and was thus much younger than the more interesting results. In future it could cave bears. Further investigations, inclu- be possible to separate this bear taxonomi- ding new 14C-datings and DNA-Analyses cally as a new, persisting subspecies of U. will shed some more light on this big deningeri. See also RABEDER & NAGEL brown bear. (this volume). And last but not least there is the pro- blem of the bears from Conturines cave (Southern Tyrol, Italy) showing characters CONCLUSIONS from U.
Recommended publications
  • Morphometric Analyses of Cave Bear Mandibles (Carnivora, Ursidae)
    Revue de Paléobiologie, Genève (décembre 2018) 37 (2): 379-393 ISSN 0253-6730 Morphometric analyses of cave bear mandibles (Carnivora, Ursidae) Gennady F. BARYSHNIKOV1*, Andrei Yu. PUZACHENKO2 & Svetlana V. BARYSHNIKOVA1 1 Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, 199034 Saint Petersburg, Russia 2 Institute of Geography, Russian Academy of Sciences, Staromonetnyi per. 29, 109017 Moscow, Russia * Corresponding author: E-mail: [email protected] Abstract Morphometric variability of cave and brown bears and their ancestors (Ursus minimus and U. etruscus) is examined using multivariate statistics based on measurements of 679 mandibles from 90 localities in Northern Eurasia. The variability is dependent on sexual dimorphism in size: it is well seen in big cave bears (U. spelaeus, U. kanivetz = ingressus, U. kudarensis), whose males are nearly 25% larger than females. In the morphological space, we identified two main types of mandibles: the “arctoid” type [U. minimus, U. etruscus, U. arctos, U. rodei (?)], and the “spelaeoid” type (U. spelaeus spelaeus, U. s. eremus, U. kanivetz, U. kudarensis). The intermediate “deningeroid” type includes U. deningeri, U. savini, U. rossicus (males), and U. spelaeus ladinicus. An additional unit is formed by female sample of U. rossicus. The mandible bones are less informative for understanding of cave bear evolution, because in comparison to crania, they have a rather simple shape. Keywords Ursus, cave bears, morphometrics, variations, mandible, evolution, adaptation, Pleistocene. Résumé Analyse morphométrique de la mandibule chez les ours des cavernes. - La variabilité morphométrique des ours des cavernes, des ours bruns et de leurs ancêtres (Ursus minimus et U. etruscus) est étudiée à partir des mesures de 679 mandibules de 90 sites d’Eurasie du nord, à l’aide des méthodes d’analyses statistiques multivariées.
    [Show full text]
  • PDF Viewing Archiving 300
    Bull. Soc. belge Géol., Paléont., Hydrol. T. 79 fasc. 2 pp. 167-174 Bruxelles 1970 Bull. Belg. Ver. Geol., Paleont., Hydrol. V. 79 deel 2 blz. 167-174 Brussel 1970 MAMMALS OF THE CRAG AND FOREST BED B. McW1LLIAMs SuMMARY. In the Red and Norwich Crags mastodonts gradually give way to the southern elephant, large caballine horses and deer of the Euctenoceros group become common. Large rodents are represented by Castor, Trogontherium and rarely Hystrix; small forms include species of Mimomys. Carnivores include hyaena, sabre-toothed cat, leopard, polecat, otter, bear, seal and walrus. The Cromer Forest Bed Series had steppe and forest forms of the southern elephant and the mastodont has been lost. Severa! species of giant deer become widespread and among the many rodents are a. number of voles which develop rootless cheek teeth. The mole is common. Warmth indicators include a monkey, and more commonly hippopotamus. Possible indicators of cold include glutton and musk ox. Rhinoceros is widespread, and it is a time of rapid evolution for the elk. Carnivores include hyaena, bear, glutton, polecat, marten, wold and seal. The interpretation of mammalian finds from is represented by bones which resemble the the Crags and Forest Bed is not an easy mole remains but are about twice their size. matter. A proportion of the remains have been derived from eatlier horizons, others are Order Primates discovered loose in modern coastal deposits, and early collectors often kept inadequate The order is represented at this period m records. Owing to the uncertain processes of England by a single record of Macaca sp., the fossilisation or inadequate collecting there are distal end of a teft humerus from a sandy many gaps in our knowledge of the mammal­ horizon of the Cromerian at West Runton, ian faunas of these times.
    [Show full text]
  • Growth Trajectories in the Cave Bear and Its Extant
    Fuchs et al. BMC Evolutionary Biology (2015) 15:239 DOI 10.1186/s12862-015-0521-z RESEARCH ARTICLE Open Access Growth trajectories in the cave bear and its extant relatives: an examination of ontogenetic patterns in phylogeny Manuela Fuchs, Madeleine Geiger*, Madlen Stange and Marcelo R. Sánchez-Villagra Abstract Background: The study of postnatal ontogeny can provide insights into evolution by offering an understanding of how growth trajectories have evolved resulting in adult morphological disparity. The Ursus lineage is a good subject for studying cranial and mandibular shape and size variation in relation to postnatal ontogeny and phylogeny because it is at the same time not diverse but the species exhibit different feeding ecologies. Cranial and mandibular shapes of Ursus arctos (brown bear), U. maritimus (polar bear), U. americanus (American black bear), and the extinct U. spelaeus (cave bear) were examined, using a three-dimensional geometric morphometric approach. Additionally, ontogenetic series of crania and mandibles of U. arctos and U. spelaeus ranging from newborns to senile age were sampled. Results: The distribution of specimens in morphospace allowed to distinguish species and age classes and the ontogenetic trajectories U. arctos and U. spelaeus were found to be more similar than expected by chance. Cranial shape changes during ontogeny are largely size related whereas the evolution of cranial shape disparity in this clade appears to be more influenced by dietary adaptation than by size and phylogeny. The different feeding ecologies are reflected in different cranial and mandibular shapes among species. Conclusions: The cranial and mandibular shape disparity in the Ursus lineage appears to be more influenced by adaptation to diet than by size or phylogeny.
    [Show full text]
  • Pleistocene Panthera Leo Spelaea
    Quaternaire, 22, (2), 2011, p. 105-127 PLEISTOCENE PANTHERA LEO SPELAEA (GOLDFUSS 1810) REMAINS FROM THE BALVE CAVE (NW GERMANY) – A CAVE BEAR, HYENA DEN AND MIDDLE PALAEOLITHIC HUMAN CAVE – AND REVIEW OF THE SAUERLAND KARST LION CAVE SITES n Cajus G. DIEDRICH 1 ABSTRACT Pleistocene remains of Panthera leo spelaea (Goldfuss 1810) from Balve Cave (Sauerland Karst, NW-Germany), one of the most famous Middle Palaeolithic Neandertalian cave sites in Europe, and also a hyena and cave bear den, belong to the most im- portant felid sites of the Sauerland Karst. The stratigraphy, macrofaunal assemblages and Palaeolithic stone artefacts range from the final Saalian (late Middle Pleistocene, Acheulean) over the Middle Palaeolithic (Micoquian/Mousterian), and to the final Palaeolithic (Magdalénien) of the Weichselian (Upper Pleistocene). Most lion bones from Balve Cave can be identified as early to middle Upper Pleistocene in age. From this cave, a relatively large amount of hyena remains, and many chewed, and punctured herbivorous and carnivorous bones, especially those of woolly rhinoceros, indicate periodic den use of Crocuta crocuta spelaea. In addition to those of the Balve Cave, nearly all lion remains in the Sauerland Karst caves were found in hyena den bone assemblages, except those described here material from the Keppler Cave cave bear den. Late Pleistocene spotted hyenas imported most probably Panthera leo spelaea body parts, or scavenged on lion carcasses in caves, a suggestion which is supported by comparisons with other cave sites in the Sauerland Karst. The complex taphonomic situation of lion remains in hyena den bone assemblages and cave bear dens seem to have resulted from antagonistic hyena-lion conflicts and cave bear hunting by lions in caves, in which all cases lions may sometimes have been killed and finally consumed by hyenas.
    [Show full text]
  • Cave Bear Ecology and Interactions With
    CAVEBEAR ECOLOGYAND INTERACTIONSWITH PLEISTOCENE HUMANS MARYC. STINER, Department of Anthropology,Building 30, Universityof Arizona,Tucson, AZ 85721, USA,email: [email protected] Abstract:Human ancestors (Homo spp.), cave bears(Ursus deningeri, U. spelaeus), andbrown bears (U. arctos) have coexisted in Eurasiafor at least one million years, andbear remains and Paleolithic artifacts frequently are found in the same caves. The prevalenceof cave bearbones in some sites is especiallystriking, as thesebears were exceptionallylarge relative to archaichumans. Do artifact-bearassociations in cave depositsindicate predation on cave bearsby earlyhuman hunters, or do they testify simply to earlyhumans' and cave bears'common interest in naturalshelters, occupied on different schedules?Answering these and other questions aboutthe circumstancesof human-cave bear associationsis made possible in partby expectations developedfrom research on modem bearecology, time-scaledfor paleontologicand archaeologic applications. Here I review availableknowledge on Paleolithichuman-bear relations with a special focus on cave bears(Middle Pleistocene U. deningeri)from YarimburgazCave, Turkey.Multiple lines of evidence show thatcave bearand human use of caves were temporallyindependent events; the apparentspatial associations between human artifacts andcave bearbones areexplained principally by slow sedimentationrates relative to the pace of biogenicaccumulation and bears' bed preparationhabits. Hibernation-linkedbehaviors and population characteristics of cave
    [Show full text]
  • Cave Bears and Ancient DNA: a Mutually Beneficial Relationship
    Berichte der Geologischen Bundesanstalt 132 Cave bears and ancient DNA: a mutually beneficial relationship Axel Barlow 1, Michael Hofreiter 1 and Michael Knapp 2 Abstract For almost 30 years, cave bears and paleogenetic research have shared a mutually beneficial relation- ship. Due to the abundance and frequently good preservation of cave bear bones, they have often been the tissue of choice to develop and test molecular approaches aimed at recovering and sequencing DNA from ancient remains. Our understanding of cave bear biology has similarly profited from the molecular data produced through paleogenetic studies. DNA data has complemented morphologi- cal data to provide insights into the evolution and phylogeny of cave bears. Molecular population dynamic studies have helped develop hypotheses explaining the extinction of cave bears, and new genomic data is now promising to shed light on evolutionary and population genetic processes that could previously only be obtained from living species. Here we evaluate and review the role cave bears have played in the development of paleogenetic research as well as the role that paleogenetic research has had in understanding cave bear biology. We provide a perspective on where this mutually beneficial relationship is likely to take us in the near future. Zusammenfassung Seit fast 30 Jahren verbindet die Höhlenbären- und paläogenetische Forschung eine, für beide Seiten vorteilhafte, Beziehung. Aufgrund der Fülle und häufig guten Erhaltung von Höhlenbär-Knochen waren sie häufig das Material der Wahl, um molekulare Ansätze zur Extraktion und Sequenzierung von DNA aus Fossilien zu entwickeln und zu testen. Unser Verständnis der Biologie des Höhlen- bären hat in ähnlicher Weise von den molekularen Daten aus paläogenetischen Studien profitiert.
    [Show full text]
  • 299947 108 1964.Pdf
    SOCIETAS PRO FAUNA ET FLORA FE.NNICA SOCIETAS PRO FAUNA ET FLORA FENNICA ACTA ZOOLOGICA FENNICA 108 Bjom Kurten: The evolution of the Polar Bear, U rsus maritimus Phipps p- ) A. ~NA ET • .P A .fJl!N'NICA_ HELSINKI-HELSINGFORS 1964 ACTA ZOOLOGICA FENNICA 1-45 vide Acta Zoologica Fennica 45-50. 46-59 vide Acta Zoologica Fennica 60-93. 60. Alex. Luther: Untersuchungen an rhahdocoelen Turbellarien. IX. Zur Kenntnis einiger Typhloplaniden. X. "Ober Astrotorhynchus bifidus (M'Int). 42 S. (1950). 61. T. H. Jilrri: Die Kleinmarlinenbestiinde in ihren Beziehungen zu der Umwelt (Coregonus albula L.). 116 S. (1950). 62. Pontus Palmgren: Die Spinnenfauna Finnlands und Ostfennoskandiens. Ill. Xysticidae und Philodromidae. 43 S. (1950). 63. Sven Nordberg: Researches on the bird fauna of the marine zone in the Aland Archipelago. 62 pp. (1950). 64. Floriano Papil "Ober einige Typhloplaninen (Turbellaria neorhabdocoela). 20 S. (1951). 65. Einari Merikallio: On the numbers of land-birds in Finland. 16 pp. (1951). 66. K. 0. Donner: The visual acuity of some Passerine birds. 40 pp. (1951). 67. Lars von Haartman: Der Trauerfliegenschniipper. II. Populationsprobleme. 60S. (1951). 68. Erie Fabrieius: Zur Ethologie junger Anatiden. 178 S. (1951). 69. Tor G. Karling: Studien iiber Kalyptorhynchien (Turbellaria). IV. Einige Euka­ lyptorhynchia. 49 S. (1952). 70. L. Benick t: Pilzkiifer und Kliferpilze. Okologische und statistische Untersuchun­ gen. 250 S. (1952). 71. Bo-Jungar Wikgren: Osmotic regulation in some aquatic animals with special reference to the influence of temperature. 102 pp. (1953). 72. Wollram Noodt: Entromostracen aus dem Litoral und dem Kiistengrundwasser des Finnischen Meerbusens. 12 S. (1953). 73.
    [Show full text]
  • The Carnivore Remains from the Sima De Los Huesos Middle Pleistocene Site
    N. Garcia & The carnivore remains from the Sima de J. L. Arsuaga los Huesos Middle Pleistocene site Departamento de Paleontologia, (Sierra de Atapuerca, Spain) Facultad de Ciencias Geologicas, U.A. de Paleoantropologia & Instituto de View metadata, citation and similar papersRemain ats ocore.ac.ukf carnivores from the Sima de los Huesos sitebrought representin to you gby a t COREleast Geologia Economica, Universidad 158 adult individuals of a primitive (i.e., not very speleoid) form of Ursus Complutense de Madrid, Ciudad provided by Servicio de Coordinación de Bibliotecas de la... deningeri Von Reichenau 1906, have been recovered through the 1995 field Universitaria, 28040 Madrid, Spain season. These new finds extend our knowledge of this group in the Sierra de Atapuerca Middle Pleistocene. Material previously classified as Cuoninae T. Torres indet. is now assigned to Canis lupus and a third metatarsal assigned in 1987 to Departamento de Ingenieria Geoldgica, Panthera cf. gombaszoegensis, is in our opinion only attributable to Panthera sp. The Escuela Tecnica Superior de Ingenieros family Mustelidae is added to the faunal list and includes Maites sp. and a de Minas, Universidad Politecnica smaller species. The presence of Panthera leo cf. fossilis, Lynxpardina spelaea and de Madrid, Rios Rosas 21, Fells silvestris, is confirmed. The presence of a not very speloid Ursus deningeri, 28003 Madrid, Spain together with the rest of the carnivore assemblage, points to a not very late Middle Pleistocene age, i.e., oxygen isotope stage 7 or older. Relative frequencies of skeletal elements for the bear and fox samples are without major biases. The age structure of the bear sample, based on dental wear stages, does not follow the typical hibernation mortality profile and resembles a cata­ strophic profile.
    [Show full text]
  • The Genus Ursus in Eurasia: Dispersal Events and Stratigraphical Significance
    Riv. It. Paleont. Strat. v. 98 n,4 pp. 487-494 Marzo 7993 THE GENUS URSUS IN EURASIA: DISPERSAL EVENTS AND STRATIGRAPHICAL SIGNIFICANCE MARCO RUSTIONI* 6. PAUL MAZZA** Ke vuords: Urszs, PIio-Pleistocene. Eurasia. Riassunto. Sulla base dei risultati di precedenti studi condotti dagli stessi autori vengono riconosciuti cinque gruppi principali di orsi: Ursus gr. ninimus - thihtanus (orsi neri), Ursus gr. etuscus (orsi erruschi), Ursus gr. arctos (orsi bruni), Ursus gr, deningeri - spelaeus (orsi delle caverne) e Ursus gr. maitimus (orsi bianchi). Gli orsi neri sembrano essere scomparsi dall'Europa durante il Pliocene superiore, immigrarono nuovamente in Europa all'inizio del Pleistocene medio e scomparvero definitivamente dall'Europa all'inizio del Pleistocene superiore. Gli orsi etruschi sono presenti più o meno contemporaneamente nelle aree meridionali dell'Europa e dell'Asia nel corso del Pliocene superiore. La linea asiatica sembra scomparire alla fine di questo periodo, mentre il ceppo europeo soprawisse, dando origine, nel corso del Pleistocene inferiore, ai rappresentanti più evoluti. Gli orsi bruni si sono probabilmente originati in Asia. Questo gruppo si diffuse ampiamente nella regione oloartica differenziandòsi in un gran numero di varietà e presumibilmente raggiunse I'Europa alla fine del Pleistocene inferiore. L'arrivo degli orsi bruni in Europa è un evento significativo, che all'incirca coincise con il grande rinnovamento faunistico del passaggio Pleistocene inferiore-Pleistocene medio. Gli orsi bruni soppiantarono gli orsi etruschi, tipici dei contesti faunistici villafranchiani, e dettero origine alla linea degli orsi delle caverne. Gli orsi delle caverne ebbero grande successo in Europa nel Pleistocene medio e superiore e scomparvero alla fine dell'ultima glaciazione quaternaria o nel corso del primo Olocene.
    [Show full text]
  • Faced Bear, Arctotherium, from the Pleistocene of California
    I. RELATIONSHIPS AND STRUCTURE OF THE SHORT~ FACED BEAR, ARCTOTHERIUM, FROM THE PLEISTOCENE OF CALIFORNIA. By JOHN C. MERRIAM and CHESTER STOCK. With ten plates and five text-figures. 1 CONTENTS. PAGE Introduct-ion. 3 Systematic position of Arctotherium and its allies with relation to the typical Ursidae. 4 Origin of the Tremarctinae. 5 Summary of species of Arctotherium in the Pleistocene of North America. 7 Occurrence in California of arctotheres and associated faunas . 9 Potter Creek Cave. 9 Rancho La Brea. 10 McKittrick. .......... .... .......... ....... ...... ................. 11 Odontolo~Y. and osteology of Arctotherium. 11 DentitiOn . 11 Axial skeleton. 16 Appendicular skeleton. 21 Bibliography . 34 2 RELATIONSHIPS AND STRUCTURE OF THE SHORT-FACED BEAR, ARCTOTHERIUM, FROM THE PLEISTOCENE OF CALIFORNIA. BY JoHN C . MERRIAM AND CHESTER STocK. INTRODUCTION. The peculiar short-faced Californian bear, known as Arctotherium simum, was described by Cope in 1879 from a single specimen, con­ sisting of a skull minus the lower jaw, found by J. A. Richardson in 1878 in Potter Creek Cave on the McCloud River in northern California. Since the description of A. simum, a nearly perfect skull with lower jaw and a large quantity of additional material, representing nearly all parts of the skeleton and dentition of this species, has been obtained from the deposits of Potter Creek Cave as a result of further work carried on for the University of California by E. L. Furlong and by W. J. Sinclair in 1902 and 1903. Splendid material of Arctotherium has also been secured in the Pleistocene asphalt beds at Rancho La Brea by the Los Angeles Museum of History, Science, and Art.
    [Show full text]
  • References: Future Works
    Phylogenomics and Evolution of the Ursidae Family Department of Biology Ammary Jackson, Keanu Spencer, & Alissya Theis Fig 8. Red Panda Fig. 6. American Black Bear (Ailurus fulgens) (Ursus americanus) Introduction: Ursidae is a family of generally omnivorous mammals colloquially Objectives: Results: referred to as bears. The family consists of five genera: Ailuropoda ● To determine the relatedness among the 30 individual bear taxa. Red Panda (giant panda), Helarctos (sun bear), Melursus (sloth bear), Tremarctos Spectacled Bear ● To determine if Ailurus fulgens obtained its common Spectacled Bear (spectacled bear), and Ursus (black, brown, and polar bears) all of Polar Bear name (Red Panda) from similarities to the genes Polar Bear which are found in North and South America, Europe, Asia, and Africa Polar Bear belonging to the Ursidae family or if it’s simply based on Polar Bear (Kumar et al. 2017.) The phylogenetic relationship between Ursidae Polar Bear phenotypic attributes. Polar Bear bears and the red panda (Ailurus fulgens) has been somewhat Brown Bear inconsistent and controversial. Previous phylogenetic analyses have Brown Bear Brown Bear placed the red panda within the families Ursidae (bears), Procyonidae Polar Bear Brown Bear (raccoons), Pinnepedia (seals), and Musteloidea (raccoons and weasels, Brown Bear Brown Bear skunks, and badgers) (Flynn et al. 2000.) Determining monophyly Methods: Cave Bear Cave Bear would elucidate the evolutionary relationship between Ursidae bears Sloth Bear ● Mitochondrial gene sequences of the ATP6 and ND1 genes Sloth Bear and the Red Panda. This analysis (i) tested the monophyly of the family Sun Bear were taken from a sample of 31 species (30 Ursidae family Sun Bear Ursidae; and (ii) determined how the Red Panda fits within the Black Bear and 1 Ailuridae family).
    [Show full text]
  • Partial Genomic Survival of Cave Bears in Living Brown Bears
    ARTICLES https://doi.org/10.1038/s41559-018-0654-8 Partial genomic survival of cave bears in living brown bears Axel Barlow 1,16*, James A. Cahill 2,16, Stefanie Hartmann1, Christoph Theunert3,4, Georgios Xenikoudakis1, Gloria G. Fortes1,5, Johanna L. A. Paijmans1, Gernot Rabeder6, Christine Frischauf6, Aurora Grandal-d’Anglade7, Ana García-Vázquez7, Marine Murtskhvaladze8, Urmas Saarma9, Peeter Anijalg9, Tomaž Skrbinšek10, Giorgio Bertorelle5, Boris Gasparian11, Guy Bar-Oz12, Ron Pinhasi13,14, Montgomery Slatkin3, Love Dalén15, Beth Shapiro2 and Michael Hofreiter1 Although many large mammal species went extinct at the end of the Pleistocene epoch, their DNA may persist due to past episodes of interspecies admixture. However, direct empirical evidence of the persistence of ancient alleles remains scarce. Here, we present multifold coverage genomic data from four Late Pleistocene cave bears (Ursus spelaeus complex) and show that cave bears hybridized with brown bears (Ursus arctos) during the Pleistocene. We develop an approach to assess both the directionality and relative timing of gene flow. We find that segments of cave bear DNA still persist in the genomes of living brown bears, with cave bears contributing 0.9 to 2.4% of the genomes of all brown bears investigated. Our results show that even though extinction is typically considered as absolute, following admixture, fragments of the gene pool of extinct species can survive for tens of thousands of years in the genomes of extant recipient species. t is increasingly apparent that admixture among closely related syntopy in Eurasia for hundreds of thousands of years14,15 before mammalian species may have occurred frequently over the course extinction of the cave bear.
    [Show full text]