LESSON 8 CARNIVORES Aim Describe the Distinguishing
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Pygmy Hog – 1 Southern Ningaul – 16 Kowari – 9 Finlayson's Squirrel
Pygmy Hog – 1 Habitat: Diurnal/Nocturnal Defense: Size Southern Ningaul – 16 Habitat: Diurnal/Nocturnal Defense: Size Kowari – 9 Habitat: Diurnal/Nocturnal Defense: Size Finlayson’s Squirrel – 8 Habitat: Diurnal/Nocturnal Defense: Size Kodkod – 5 Habitat: Diurnal/Nocturnal Defense: Size Least Chipmunk – 12 Habitat: Diurnal/Nocturnal Defense: Size Tree Hyrax – 4 Habitat: Diurnal/Nocturnal Defense: Size Bank Vole – 13 Habitat: Diurnal/Nocturnal Defense: Size Island Fox – 6 Habitat: Diurnal/Nocturnal Defense: Size Gray-bellied Caenolestid – 11 Habitat: Diurnal/Nocturnal Defense: Size Raccoon Dog – 3 Habitat: Diurnal/Nocturnal Defense: Size Northern Short-Tailed Shrew – 14 Habitat: Diurnal/Nocturnal Defense: Size Southern African Hedgehog - 7 Habitat: Diurnal/Nocturnal Defense: Size Collard Pika - 10 Habitat: Diurnal/Nocturnal Defense: Size Pudu – 2 Habitat: Diurnal/Nocturnal Defense: Size Seba’s Short-tailed Bat – 15 Habitat: Diurnal/Nocturnal Defense: Size Pygmy Spotted Skunk - 16 Habitat: Diurnal/Nocturnal Defense: Size Grandidier’s “Mongoose” - 16 Habitat: Diurnal/Nocturnal Defense: Size Sloth Bear - 1 Habitat: Diurnal/Nocturnal Defense: Size Spotted Linsing - 9 Habitat: Diurnal/Nocturnal Defense: Size Red Panda - 8 Habitat: Diurnal/Nocturnal Defense: Size European Badger – 5 Habitat: Diurnal/Nocturnal Defense: Size Giant Forest Genet – 12 Habitat: Diurnal/Nocturnal Defense: Size African Civet – 4 Habitat: Diurnal/Nocturnal Defense: Size Kinkajou – 13 Habitat: Diurnal/Nocturnal Defense: Size Fossa – 6 Habitat: Diurnal/Nocturnal Defense: -
First Sighting of the Giant Genet Genetta Victoriae in Rwanda
First sighting of the Giant Genet Genetta victoriae in Rwanda Vladimir DINETS Abstract A large genet photographed in 2005 in Nyungwe National Park, Rwanda, was identified as a Giant GenetGenetta victoriae, previously known with certainty only from the Democratic Republic of Congo and the adjacent part of Uganda and never before photographed in the wild. Keywords: montane rainforest, Nyungwe National Park, spotlighting, Viverridae Première observation de la Genette Géante Genetta victoriae au Rwanda Résumé Une genette de grande taille photographiée en 2005 dans le Parc National de Nyungwe au Rwanda, est identifiée comme représentant la Genette Géante Genetta victoriae ; cette espèce n’était connue que de la République Démocratique du Congo et de la partie limitrophe de l’Ouganda, et n’avait jamais été photographiée dans la nature. Mots clés: forêt ombrophile de montagne, Parc National de Nyungwe, spotlighting, Viverridae Giant Genet Genetta victoriae Thomas, 1901 is an enigmatic car- nivoran species, currently known with certainty only from northern and eastern parts of the Democratic Republic of Congo (DRC), where it inhabits lowland and montane rainforests up to 2,000 m (Van Rompaey et al. 2008). It has been predicted to occur in Rwan- da and Uganda, but there are no confirmed observations or mu- seum specimens from outside DRC (Gaubert et al. 2006), except in Semiliki Forest in Uganda on the border with DRC (Bere 1962). A captive specimen has been photographed by Rahm (1966), but there are no photos obtained in the wild, and no published infor- mation on wild animals, except for observations by Kingdon (1977) in Uganda, which appear questionable (Schreiber et al. -
Mammalia, Carnivora) from the Blancan of Florida
THREE NEW PROCYONIDS (MAMMALIA, CARNIVORA) FROM THE BLANCAN OF FLORIDA Laura G. Emmert1,2 and Rachel A. Short1,3 ABSTRACT Fossils of the mammalian family Procyonidae are relatively abundant at many fossil localities in Florida. Analysis of specimens from 16 late Blancan localities from peninsular Florida demonstrate the presence of two species of Procyon and one species of Nasua. Procyon gipsoni sp. nov. is slightly larger than extant Procyon lotor and is distinguished by five dental characters including a lack of a crista between the para- cone and hypocone on the P4, absence of a basin at the lingual intersection of the hypocone and protocone on the P4, and a reduced metaconule on the M1. Procyon megalokolos sp. nov. is significantly larger than extant P. lotor and is characterized primarily by morphology of the postcrania, such as an expanded and posteriorly rotated humeral medial epicondyle, more prominent tibial tuberosity, and more pronounced radioulnar notch. Other than larger size, the dentition of P. megalokolos falls within the range of variation observed in extant P. lotor, suggesting that it may be an early member of the P. lotor lineage. Nasua mast- odonta sp. nov. has a unique accessory cusp on the m1 as well as multiple morphological differences in the dentition and postcrania, such as close appression of the trigonid of the m1 and a less expanded medial epicondyle of the humerus. We also synonymize Procyon rexroadensis, formerly the only known Blancan Procyon species in North America, with P. lotor due to a lack of distinct dental morphological features observed in specimens from its type locality in Kansas. -
Rapid Range Expansion of the Feral Raccoon (Procyon Lotor) in Kanagawa Prefecture, Japan, and Its Impact on Native Organisms
Rapid range expansion of the feral raccoon (Procyon lotor) in Kanagawa Prefecture, Japan, and its impact on native organisms Hisayo Hayama, Masato Kaneda, and Mayuh Tabata Kanagawa Wildlife Support Network, Raccoon Project. 1-10-11-2 Takamoridai, Isehara 259-1115, Kanagawa, Japan Abstract The distribution of feral raccoons (Procyon lotor) was surveyed in Kanagawa Prefecture, central Japan. Information was collected mainly through use of a questionnaire to municipal offices, environment NGOs, and hunting specialists. The raccoon occupied 26.5% of the area of the prefecture, and its distribution range doubled over three years (2001 to 2003). The most remarkable change was the range expansion of the major population in the south-eastern part of the prefecture, and several small populations that were found throughout the prefecture. Predation by feral raccoons on various native species probably included endangered Tokyo salamanders (Hynobius tokyoensis), a freshwater Asian clam (Corbicula leana), and two large crabs (Helice tridens and Holometopus haematocheir). The impact on native species is likely to be more than negligible. Keywords: Feral raccoon; Procyon lotor; distribution; questionnaire; invasive alien species; native species; Kanagawa Prefecture INTRODUCTION The first record of reproduction of the feral raccoon presence of feral raccoons between 2001 and 2003 in Kanagawa Prefecture was from July 1990, and it and the reliability of the information. One of the was assumed that the raccoon became naturalised in issues relating to reliability is possible confusion with this prefecture around 1988 (Nakamura 1991). the native raccoon dog (Nyctereutes procyonoides; Damage by feral raccoons is increasing and the Canidae), which has a similar facial pattern with a number of raccoons, captured as part of the wildlife black band around the eyes, and a similar body size to pest control programme, is also rapidly increasing. -
Supplemental File 1: Addressing Claims of “Zombie” Lineages on Phillips’ (2016) Timetree
Supplemental File 1: Addressing claims of “zombie” lineages on Phillips’ (2016) timetree The soft explosive model of placental mammal evolution Matthew J. Phillips*,1 and Carmelo Fruciano1 1School of Earth, Environmental and Biological Sciences, Queensland University of Technology, Brisbane, Australia *Corresponding author: E-mail: [email protected] Contents Addressing claims of “zombie” lineages on Phillips’ (2016) timetree ................................................... 1 Incorrect or poorly supported fossil placements ................................................................................. 1 Figure S1 ............................................................................................................................................ 4 Table S1 .............................................................................................................................................. 6 References .............................................................................................................................................. 7 Addressing claims of “zombie lineages” on Phillips’ (2016) timetree Phillips [1] found extreme divergence underestimation among large, long-lived taxa that were not calibrated, and argued that calibrating these taxa instead shifted the impact of the underlying rate model misspecification to inflating dates deeper in the tree. To avoid this “error-shift inflation”, Phillips [1] first inferred divergences with dos Reis et al.’s [2] calibrations, most of which are set among taxa -
TROUBLE-MAKING BROWN BEAR URSUS ARCTOS LINNAEUS, 1758 (MAMMALIA: CARNIVORA) – Behavioral PATTERN ANALYSIS of the SPECIALIZED INDIVIDUALS
Travaux du Muséum National d’Histoire Naturelle © 30 Décembre Vol. LIV (2) pp. 541–554 «Grigore Antipa» 2011 DOI: 10.2478/v10191-011-0032-0 TROUBLE-MAKING BROWN BEAR URSUS ARCTOS LINNAEUS, 1758 (MAMMALIA: CARNIVORA) – BEHAVIORal PATTERN ANALYSIS OF THE SPECIALIZED INDIVIDUALS LEONARDO BERECZKY, MIHAI POP, SILVIU CHIRIAC Abstract. In Romania more than 500 damage cases caused by large carnivores are reported by livestock owners and farmers each year. This is the main reason for hunting derogation despite the protected species status. This study is the result of detailed examination of 198 damage cases caused by bears in 2008 and 2009, in the south- eastern Carpathian Mts in Romania. The goal of the study was to examine whether an individual-specific behavioural pattern among problematic bears exists. We looked for bears which showed repeated killing of livestock, a phenomenon claimed by livestock owners to indicate the presence of a problematic individual in the area. In 27% of the observed cases the problematic bears exhibited specific behaviour patterns: clear specialization on a certain type of damage, high degree of tolerance for humans, selectivity for certain prey items, returning back to the damage site in less than 8 days. Fast adaptation and taking advantage of easily obtainable food around human created artificial sources is characteristic for all bear species, due to their high learning capacity and ecological plasticity, but from the conservation and management point of view dealing with individuals which specialize to live mainly around artificial areas becomes a “problem”. Thus defining and identifying individual behaviour patterns oriented towards conflicting behaviour might be useful for wildlife managers in identifying “problem individuals” in order to apply the proper control methods. -
Hyaenodontidae (Creodonta, Mammalia) and the Position of Systematics in Evolutionary Biology
Hyaenodontidae (Creodonta, Mammalia) and the Position of Systematics in Evolutionary Biology by Paul David Polly B.A. (University of Texas at Austin) 1987 A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Paleontology in the GRADUATE DIVISION of the UNIVERSITY of CALIFORNIA at BERKELEY Committee in charge: Professor William A. Clemens, Chair Professor Kevin Padian Professor James L. Patton Professor F. Clark Howell 1993 Hyaenodontidae (Creodonta, Mammalia) and the Position of Systematics in Evolutionary Biology © 1993 by Paul David Polly To P. Reid Hamilton, in memory. iii TABLE OF CONTENTS Introduction ix Acknowledgments xi Chapter One--Revolution and Evolution in Taxonomy: Mammalian Classification Before and After Darwin 1 Introduction 2 The Beginning of Modern Taxonomy: Linnaeus and his Predecessors 5 Cuvier's Classification 10 Owen's Classification 18 Post-Darwinian Taxonomy: Revolution and Evolution in Classification 24 Kovalevskii's Classification 25 Huxley's Classification 28 Cope's Classification 33 Early 20th Century Taxonomy 42 Simpson and the Evolutionary Synthesis 46 A Box Model of Classification 48 The Content of Simpson's 1945 Classification 50 Conclusion 52 Acknowledgments 56 Bibliography 56 Figures 69 Chapter Two: Hyaenodontidae (Creodonta, Mammalia) from the Early Eocene Four Mile Fauna and Their Biostratigraphic Implications 78 Abstract 79 Introduction 79 Materials and Methods 80 iv Systematic Paleontology 80 The Four Mile Fauna and Wasatchian Biostratigraphic Zonation 84 Conclusion 86 Acknowledgments 86 Bibliography 86 Figures 87 Chapter Three: A New Genus Eurotherium (Creodonta, Mammalia) in Reference to Taxonomic Problems with Some Eocene Hyaenodontids from Eurasia (With B. Lange-Badré) 89 Résumé 90 Abstract 90 Version française abrégéé 90 Introduction 93 Acknowledgments 96 Bibliography 96 Table 3.1: Original and Current Usages of Genera and Species 99 Table 3.2: Species Currently Included in Genera Discussed in Text 101 Chapter Four: The skeleton of Gazinocyon vulpeculus n. -
Dental Anomalies in the Atlantic Population of South American Sea Lion, Otaria Byronia (Pinnipedia, Otariidae): Evolutionary Implications and Ecological Approach
e-ISSN 2236-1057 - doi:10.5597/lajam00044 http://dx.doi.org/10.5597/lajam00044 LAJAM 3(1): 7-18, January/June 2004 ISSN 1676-7497 DENTAL ANOMALIES IN THE ATLANTIC POPULATION OF SOUTH AMERICAN SEA LION, OTARIA BYRONIA (PINNIPEDIA, OTARIIDAE): EVOLUTIONARY IMPLICATIONS AND ECOLOGICAL APPROACH César Jaeger Drehmer 1, 2 , Marta Elena Fabián 2, 3 and João Oldair Menegheti 3 Abstract – We analyzed 63 cases of dental anomalies from 62 specimens of a total sample of 516 specimens of the Atlantic population of South American sea lions, Otaria byronia de Blainville, 1820. The anomalies were represented by 53 cases of missing upper post-canine 6 (second molars), seven cases of maxillary or mandibular extra teeth, two cases of “dentes geminati” and one case of reduced teeth. Considering a phylogenetic framework where all otariid species and basal Pinnipedimorpha are included, missing post-canine 6 could be related to evolutionary trends in Otariidae towards a progressive reduction and loss of teeth (agenesis). The occurrence of the upper post-canine 6 in Otaria Péron, 1816 as in Phocarctos Peters, 1866 is usually regarded as a primitive character. Alternatively, when adopting another cladistic procedure, this could be interpreted as a taxic atavism at the base of Otaria/Phocarctos clade. Extra-mandibular teeth are related to a concrete case of spontaneous atavism in the dentition of Otaria byronia, in retrogression to ancient groups like the Miocene pinnipediform Pteronarctos Barnes, 1989. The other anomalies – maxillary extra teeth, “dentes geminati” and reduced teeth - are caused by some disturbance on the epigenetic system underlying dental morphogenesis leading to duplication, coalescence or duplication and reduction of the dental germ, respectively. -
American Black Bear (Ursus Americanus)
FIELD GUIDE TO NORTH AMERICAN MAMMALS American Black Bear (Ursus americanus) ORDER: Carnivora FAMILY: Ursidae Most Black Bears hibernate for up to seven months, and do not eat, drink, urinate, or exercise the entire time. In the South, where plant food is available all year, not all bears hibernate—but pregnant females do. The female gives birth to 1−6 cubs (usually 2 or 3) in January, while she is deep asleep in her den. The newborn cubs Ursus americanus − eastern, black variant snuggle next to her for warmth and nurse while she fasts. They grow Credit: painting by Consie Powell from Kays and Wilson's Mammals of North America, © Princeton University Press from a birth weight of 200−450 g each (about 7−16 pounds) to the (2002) 2−5 kg they will weigh when the family leaves the den in the spring. Black Bears eat a little meat, and some insects, but they rely on fruit, nuts, and vegetation for the bulk of their nutritional needs. They are not all black. Most are, with brown muzzles, but in some western forests they are brown, cinnamon, or blond, and a few, in southern Alaska and British Columbia, are creamy white or bluish−gray. Also known as: Many common names are given to the many subspecies that have been described, such as: Olympic Black Bear, Glacier Bear, California Black Bear, Florida Black Bear. Sexual Dimorphism: The largest males may be nearly twice as heavy as the heaviest females. Length: Range: 1,44−2,000 mm males; 1,200−1,600 mm females Weight: Average: 120 kg males; 80 kg females Range: 47−409 kg males; 39−236 kg females http://www.mnh.si.edu/mna 1 FIELD GUIDE TO NORTH AMERICAN MAMMALS Brown Bear, Grizzly Bear (Ursus arctos) ORDER: Carnivora FAMILY: Ursidae Conservation Status: The Mexican Grizzly Bear, Ursus arcos nelsoni, is Extinct. -
The 2008 IUCN Red Listings of the World's Small Carnivores
The 2008 IUCN red listings of the world’s small carnivores Jan SCHIPPER¹*, Michael HOFFMANN¹, J. W. DUCKWORTH² and James CONROY³ Abstract The global conservation status of all the world’s mammals was assessed for the 2008 IUCN Red List. Of the 165 species of small carni- vores recognised during the process, two are Extinct (EX), one is Critically Endangered (CR), ten are Endangered (EN), 22 Vulnerable (VU), ten Near Threatened (NT), 15 Data Deficient (DD) and 105 Least Concern. Thus, 22% of the species for which a category was assigned other than DD were assessed as threatened (i.e. CR, EN or VU), as against 25% for mammals as a whole. Among otters, seven (58%) of the 12 species for which a category was assigned were identified as threatened. This reflects their attachment to rivers and other waterbodies, and heavy trade-driven hunting. The IUCN Red List species accounts are living documents to be updated annually, and further information to refine listings is welcome. Keywords: conservation status, Critically Endangered, Data Deficient, Endangered, Extinct, global threat listing, Least Concern, Near Threatened, Vulnerable Introduction dae (skunks and stink-badgers; 12), Mustelidae (weasels, martens, otters, badgers and allies; 59), Nandiniidae (African Palm-civet The IUCN Red List of Threatened Species is the most authorita- Nandinia binotata; one), Prionodontidae ([Asian] linsangs; two), tive resource currently available on the conservation status of the Procyonidae (raccoons, coatis and allies; 14), and Viverridae (civ- world’s biodiversity. In recent years, the overall number of spe- ets, including oyans [= ‘African linsangs’]; 33). The data reported cies included on the IUCN Red List has grown rapidly, largely as on herein are freely and publicly available via the 2008 IUCN Red a result of ongoing global assessment initiatives that have helped List website (www.iucnredlist.org/mammals). -
Phylogenomic Systematics of the Spotted Skunks (Carnivora, Mephitidae, Spilogale)
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.23.353045; this version posted October 25, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Phylogenomic systematics of the spotted skunks (Carnivora, Mephitidae, Spilogale): 2 Additional species diversity and Pleistocene climate change as a major driver of 3 diversification 4 Molly M. McDonough*,†, Adam W. Ferguson*, Robert C. Dowler, Matthew E. Gompper, and 5 Jesús E. Maldonado 6 *-Equally contributing lead authors 7 †-Corresponding Author 8 Molly M. McDonough, Ph.D. 9 Chicago State University 10 Department of Biological Sciences 11 9501 S. King Drive, WSC 290 12 Chicago, IL 60628-1598 13 [email protected] 14 (773) 995-2443 15 16 17 Abstract 18 Four species of spotted skunks (Carnivora, Mephitidae, Spilogale) are currently recognized: 19 Spilogale angustifrons, S. gracilis, S. putorius, and S. pygmaea. Understanding species 20 boundaries within this group is critical for effective conservation given that regional populations 21 or subspecies (e.g., S. p. interrupta) have experienced significant population declines. Further, 22 there may be currently unrecognized diversity within this genus as some taxa (e.g., S. 23 angustifrons) and geographic regions (e.g., Central America) never have been assessed using 24 DNA sequence data. We analyzed species limits and diversification patterns in spotted skunks 25 using multilocus nuclear (ultraconserved elements) and mitochondrial (whole mitogenomes and 26 single gene analysis) data sets from broad geographic sampling representing all currently 27 recognized species and subspecies. -
University of Florida Thesis Or Dissertation Formatting
UNDERSTANDING CARNIVORAN ECOMORPHOLOGY THROUGH DEEP TIME, WITH A CASE STUDY DURING THE CAT-GAP OF FLORIDA By SHARON ELIZABETH HOLTE A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2018 © 2018 Sharon Elizabeth Holte To Dr. Larry, thank you ACKNOWLEDGMENTS I would like to thank my family for encouraging me to pursue my interests. They have always believed in me and never doubted that I would reach my goals. I am eternally grateful to my mentors, Dr. Jim Mead and the late Dr. Larry Agenbroad, who have shaped me as a paleontologist and have provided me to the strength and knowledge to continue to grow as a scientist. I would like to thank my colleagues from the Florida Museum of Natural History who provided insight and open discussion on my research. In particular, I would like to thank Dr. Aldo Rincon for his help in researching procyonids. I am so grateful to Dr. Anne-Claire Fabre; without her understanding of R and knowledge of 3D morphometrics this project would have been an immense struggle. I would also to thank Rachel Short for the late-night work sessions and discussions. I am extremely grateful to my advisor Dr. David Steadman for his comments, feedback, and guidance through my time here at the University of Florida. I also thank my committee, Dr. Bruce MacFadden, Dr. Jon Bloch, Dr. Elizabeth Screaton, for their feedback and encouragement. I am grateful to the geosciences department at East Tennessee State University, the American Museum of Natural History, and the Museum of Comparative Zoology at Harvard for the loans of specimens.