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Table 7: Species Changing IUCN Red List Status (2014-2015)
IUCN Red List version 2015.4: Table 7 Last Updated: 19 November 2015 Table 7: Species changing IUCN Red List Status (2014-2015) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2014 (IUCN Red List version 2014.3) and 2015 (IUCN Red List version 2015-4) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered, EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2014) List (2015) change version Category Category MAMMALS Aonyx capensis African Clawless Otter LC NT N 2015-2 Ailurus fulgens Red Panda VU EN N 2015-4 -
The Structure-Function Relationship of the Lung of the Australian Sea Lion Neophoca Cinerea
The Structure-Function Relationship of the Lung of the Australian Sea Liont Neophoc e clnerea by Anthony Nicholson B.V.Sc. A thesis submitted for the degree of Doctor of PhilosoPhY' Department of PathologY' UniversitY of Adelaide February 1984 Frontispiece: Group of four adull female Australian sea lions basking in the sun at Seal Bay, Kangaroo Island. ËF:æ: oo',,, 'å¡ -*-d, l--- --a - .¡* É--- .-\tb.<¡- <} b' \ .ltl '' 4 qÙ CONTENTS Page List of Figures X List of Tables xi Abstract XIV Declaration XV Acknowledge m ents I I. Introduction Chapter \ I I.I Classification of Marine Mammals I I.2', Distribution of Australian Pinnipeds 2 I.3 Diving CaPabilitY 3 PhYsiologY 1.4 Diving 4 Cardiovascular SYstem ' l'.4.I B I.4.2 OxYgen Stores 1l L.4.3 BiochemicalAdaPtations L3 I.4.4 PulmonarYFunction I.4.5 Effects oi Incteased Hydrostatic Pressure T6 l-8 1.5 SummarY and Aims 20 Chapter 2. Materials and Methods 20 ?.I Specimen Collection 2I 2.2 Lung Fixation 2I 2.3 Lung Votume Determination 22 2.4 Parasite Collection and Incubation 22 2.5 M icroscoPY 22 2.5.I Light MicroscoPY Electron Microscopy 23 2..5.2 Trãnsmission 23 2.5.3 Scanning ElectronMicroscopy 25 Chapter 5. Norm al ResPiratorY Structure 25 t.r Introduction 25 Mam maI Respiratory System 3.2 Terrestrial 25 1.2.I MacroscoPtc 27 3.2.2 MicroscoPic 27 SYstem 3.3 Pinniped ResPiratorY 27 3.3.I MacroscoPic 28 3.3.2 MicroscoPic 3I 3.4 Results 3I 1.4.L MacroscoPic 32 3.4.2 MicroscoPic 7B 3.5 Discussion 7B 3.5.I MacroscoPtc 79 3.5.2 MicroscoPic 92 3.6 SummarY IV Page Chapter 4. -
Assessment of Impacts and Potential Mitigation for Icebreaking Vessels MARK Transiting Pupping Areas of an Ice-Breeding Seal
Biological Conservation 214 (2017) 213–222 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Assessment of impacts and potential mitigation for icebreaking vessels MARK transiting pupping areas of an ice-breeding seal ⁎ Susan C. Wilsona, , Irina Trukhanovab, Lilia Dmitrievac, Evgeniya Dolgovad, Imogen Crawforda, Mirgaliy Baimukanove, Timur Baimukanove, Bekzat Ismagambetove, Meirambek Pazylbekovf, ⁎ Mart Jüssig, Simon J. Goodmanc, a Tara Seal Research, Killyleagh, Co. Down, N. Ireland, UK b Polar Science Center, Applied Physics Laboratory, University of Washington, Seattle, USA c School of Biology, Faculty of Biological Sciences, University of Leeds, Leeds, UK d Lomonosov Moscow State University, Russian Federation e Institute of Hydrobiology & Ecology, Karasaysky Raion, Almaty, Kazakhstan f Institute of Fisheries, Almaty, Kazakhstan g Pro Mare MTÜ, Saula, Kose, Harjumaa EE 75101, Estonia ARTICLE INFO ABSTRACT Keywords: Icebreaker operations in the Arctic and other areas are increasing rapidly to support new industrial activities and Caspian Sea shipping routes, but the impact on pinnipeds in these habitats is poorly explored. We present the first quantitative Pinniped study of icebreakers transiting ice-breeding habitat of a phocid seal and recommendations for mitigation. Impacts Marine mammal were recorded from the vessel bridge during seven ice seasons 2006–2013, for Caspian seals (Pusa caspica) Ship strikes breeding on the winter ice-field of the Caspian Sea. Impacts included displacement and separation of mothers and Aerial survey pups, breakage of birth or nursery sites and vessel-seal collisions. The flight distance of mothers with pups ahead Conservation was < 100 m, but measurable disturbance occurred at distances exceeding 200 m. -
56. Otariidae and Phocidae
FAUNA of AUSTRALIA 56. OTARIIDAE AND PHOCIDAE JUDITH E. KING 1 Australian Sea-lion–Neophoca cinerea [G. Ross] Southern Elephant Seal–Mirounga leonina [G. Ross] Ross Seal, with pup–Ommatophoca rossii [J. Libke] Australian Sea-lion–Neophoca cinerea [G. Ross] Weddell Seal–Leptonychotes weddellii [P. Shaughnessy] New Zealand Fur-seal–Arctocephalus forsteri [G. Ross] Crab-eater Seal–Lobodon carcinophagus [P. Shaughnessy] 56. OTARIIDAE AND PHOCIDAE DEFINITION AND GENERAL DESCRIPTION Pinnipeds are aquatic carnivores. They differ from other mammals in their streamlined shape, reduction of pinnae and adaptation of both fore and hind feet to form flippers. In the skull, the orbits are enlarged, the lacrimal bones are absent or indistinct and there are never more than three upper and two lower incisors. The cheek teeth are nearly homodont and some conditions of the ear that are very distinctive (Repenning 1972). Both superfamilies of pinnipeds, Phocoidea and Otarioidea, are represented in Australian waters by a number of species (Table 56.1). The various superfamilies and families may be distinguished by important and/or easily observed characters (Table 56.2). King (1983b) provided more detailed lists and references. These and other differences between the above two groups are not regarded as being of great significance, especially as an undoubted fur seal (Australian Fur-seal Arctocephalus pusillus) is as big as some of the sea lions and has some characters of the skull, teeth and behaviour which are rather more like sea lions (Repenning, Peterson & Hubbs 1971; Warneke & Shaughnessy 1985). The Phocoidea includes the single Family Phocidae – the ‘true seals’, distinguished from the Otariidae by the absence of a pinna and by the position of the hind flippers (Fig. -
African Clawless Otter (Aonyx Capensis) – Near Threatened (IUCN Red List)
African clawless otter (Aonyx capensis) – Near Threatened (IUCN Red List) The Cape clawless otter is large: head and body about 1 m long, tail 50 cm, and typically weighs 10 - 20 kg. Upper parts of the body are dark brown, and the chin, cheeks, throat, and chest off- white. Whiskers are very long, numerous, and white. They assist in detecting its main prey (crabs) which are captured with the dexterous clawless forefeet. In freshwater habitats, it feeds mostly on crabs, and lesser amounts of frogs, fish, and seasonally on dragonfly larvae. Otters dry and groom themselves by rolling in grass, or on sandbanks or rocks. At most rolling places latrines are established, which like the rolling places, are regularly used. While defecating a clawless otter often rotates on the spot, so the scats are dropped all around it, broken into short pieces, not tapered at both ends. When fresh scats are dark brown, changing to a cream colour as they dry out; typically, about 25 mm diameter, range 22 - 30 mm. Track is 60 – 90mm wide. Male’s larger than female’s African Otter Network – africanotternetwork.wordpress.com – African clawless Fresh scat – 20 - 32mm diameter, typically full of crab, maybe some fish. No seeds, hair. Otter scat – fresh (left); aged (below) Otter scat can be confused with marsh mongoose scat (right). Mongoose scat is smaller 15 – 22mm diameter and consists of crab, small mammal (hair), insect, bird feathers Marsh mongoose scat The African Otter Network is looking for information on current distribution: if seen please report to: [email protected] Where, when, how many, and any other observation information. -
Mammal Species Native to the USA and Canada for Which the MIL Has an Image (296) 31 July 2021
Mammal species native to the USA and Canada for which the MIL has an image (296) 31 July 2021 ARTIODACTYLA (includes CETACEA) (38) ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BALAENIDAE - bowheads and right whales 1. Balaena mysticetus – Bowhead Whale BALAENOPTERIDAE -rorqual whales 1. Balaenoptera acutorostrata – Common Minke Whale 2. Balaenoptera borealis - Sei Whale 3. Balaenoptera brydei - Bryde’s Whale 4. Balaenoptera musculus - Blue Whale 5. Balaenoptera physalus - Fin Whale 6. Eschrichtius robustus - Gray Whale 7. Megaptera novaeangliae - Humpback Whale BOVIDAE - cattle, sheep, goats, and antelopes 1. Bos bison - American Bison 2. Oreamnos americanus - Mountain Goat 3. Ovibos moschatus - Muskox 4. Ovis canadensis - Bighorn Sheep 5. Ovis dalli - Thinhorn Sheep CERVIDAE - deer 1. Alces alces - Moose 2. Cervus canadensis - Wapiti (Elk) 3. Odocoileus hemionus - Mule Deer 4. Odocoileus virginianus - White-tailed Deer 5. Rangifer tarandus -Caribou DELPHINIDAE - ocean dolphins 1. Delphinus delphis - Common Dolphin 2. Globicephala macrorhynchus - Short-finned Pilot Whale 3. Grampus griseus - Risso's Dolphin 4. Lagenorhynchus albirostris - White-beaked Dolphin 5. Lissodelphis borealis - Northern Right-whale Dolphin 6. Orcinus orca - Killer Whale 7. Peponocephala electra - Melon-headed Whale 8. Pseudorca crassidens - False Killer Whale 9. Sagmatias obliquidens - Pacific White-sided Dolphin 10. Stenella coeruleoalba - Striped Dolphin 11. Stenella frontalis – Atlantic Spotted Dolphin 12. Steno bredanensis - Rough-toothed Dolphin 13. Tursiops truncatus - Common Bottlenose Dolphin MONODONTIDAE - narwhals, belugas 1. Delphinapterus leucas - Beluga 2. Monodon monoceros - Narwhal PHOCOENIDAE - porpoises 1. Phocoena phocoena - Harbor Porpoise 2. Phocoenoides dalli - Dall’s Porpoise PHYSETERIDAE - sperm whales Physeter macrocephalus – Sperm Whale TAYASSUIDAE - peccaries Dicotyles tajacu - Collared Peccary CARNIVORA (48) CANIDAE - dogs 1. Canis latrans - Coyote 2. -
Endemism and Diversity of Small Mammals Along Two Neighboring Bornean Mountains
Endemism and diversity of small mammals along two neighboring Bornean mountains Miguel Camacho-Sanchez1,2,*, Melissa T.R. Hawkins3,4,5,*, Fred Tuh Yit Yu6, Jesus E. Maldonado3 and Jennifer A. Leonard1 1 Conservation and Evolutionary Genetics Group, Doñana Biological Station (EBD-CSIC), Sevilla, Spain 2 CiBIO—Centro de Investigação em Biodiversidade e Recursos Genéticos da Universidade do Porto, Vairão, Portugal 3 Center for Conservation Genomics, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, DC, USA 4 Department of Biological Sciences, Humboldt State University, Arcata, CA, USA 5 Division of Mammals, National Museum of Natural History, Washington, DC, USA 6 Sabah Parks, Kota Kinabalu, Sabah, Malaysia * These authors contributed equally to this work. ABSTRACT Mountains offer replicated units with large biotic and abiotic gradients in a reduced spatial scale. This transforms them into well-suited scenarios to evaluate biogeographic theories. Mountain biogeography is a hot topic of research and many theories have been proposed to describe the changes in biodiversity with elevation. Geometric constraints, which predict the highest diversity to occur in mid-elevations, have been a focal part of this discussion. Despite this, there is no general theory to explain these patterns, probably because of the interaction among different predictors with the local effects of historical factors. We characterize the diversity of small non-volant mammals across the elevational gradient on Mount (Mt.) Kinabalu (4,095 m) and Mt. Tambuyukon (2,579 m), two neighboring mountains in Borneo, Malaysia. We documented a decrease in species richness with elevation which deviates from expectations of the geometric constraints and suggests that spatial Submitted 14 February 2018 Accepted 9 September 2019 factors (e.g., larger diversity in larger areas) are important. -
Controlled Animals
Environment and Sustainable Resource Development Fish and Wildlife Policy Division Controlled Animals Wildlife Regulation, Schedule 5, Part 1-4: Controlled Animals Subject to the Wildlife Act, a person must not be in possession of a wildlife or controlled animal unless authorized by a permit to do so, the animal was lawfully acquired, was lawfully exported from a jurisdiction outside of Alberta and was lawfully imported into Alberta. NOTES: 1 Animals listed in this Schedule, as a general rule, are described in the left hand column by reference to common or descriptive names and in the right hand column by reference to scientific names. But, in the event of any conflict as to the kind of animals that are listed, a scientific name in the right hand column prevails over the corresponding common or descriptive name in the left hand column. 2 Also included in this Schedule is any animal that is the hybrid offspring resulting from the crossing, whether before or after the commencement of this Schedule, of 2 animals at least one of which is or was an animal of a kind that is a controlled animal by virtue of this Schedule. 3 This Schedule excludes all wildlife animals, and therefore if a wildlife animal would, but for this Note, be included in this Schedule, it is hereby excluded from being a controlled animal. Part 1 Mammals (Class Mammalia) 1. AMERICAN OPOSSUMS (Family Didelphidae) Virginia Opossum Didelphis virginiana 2. SHREWS (Family Soricidae) Long-tailed Shrews Genus Sorex Arboreal Brown-toothed Shrew Episoriculus macrurus North American Least Shrew Cryptotis parva Old World Water Shrews Genus Neomys Ussuri White-toothed Shrew Crocidura lasiura Greater White-toothed Shrew Crocidura russula Siberian Shrew Crocidura sibirica Piebald Shrew Diplomesodon pulchellum 3. -
Canid, Hye A, Aardwolf Conservation Assessment and Management Plan (Camp) Canid, Hyena, & Aardwolf
CANID, HYE A, AARDWOLF CONSERVATION ASSESSMENT AND MANAGEMENT PLAN (CAMP) CANID, HYENA, & AARDWOLF CONSERVATION ASSESSMENT AND MANAGEMENT PLAN (CAMP) Final Draft Report Edited by Jack Grisham, Alan West, Onnie Byers and Ulysses Seal ~ Canid Specialist Group EARlliPROMSE FOSSIL RIM A fi>MlY Of CCNSERVA11QN FUNDS A Joint Endeavor of AAZPA IUCN/SSC Canid Specialist Group IUCN/SSC Hyaena Specialist Group IUCN/SSC Captive Breeding Specialist Group CBSG SPECIES SURVIVAL COMMISSION The work of the Captive Breeding Specialist Group is made possible by gellerous colltributiolls from the following members of the CBSG Institutional Conservation Council: Conservators ($10,000 and above) Federation of Zoological Gardens of Arizona-Sonora Desert Museum Claws 'n Paws Australasian Species Management Program Great Britain and Ireland BanhamZoo Darmstadt Zoo Chicago Zoological Society Fort Wayne Zoological Society Copenhagen Zoo Dreher Park Zoo Columbus Zoological Gardens Gladys Porter Zoo Cotswold Wildlife Park Fota Wildlife Park Denver Zoological Gardens Indianapolis Zoological Society Dutch Federation of Zoological Gardens Great Plains Zoo Fossil Rim Wildlife Center Japanese Association of Zoological Parks Erie Zoological Park Hancock House Publisher Friends of Zoo Atlanta and Aquariums Fota Wildlife Park Kew Royal Botanic Gardens Greater Los Angeles Zoo Association Jersey Wildlife Preservation Trust Givskud Zoo Miller Park Zoo International Union of Directors of Lincoln Park Zoo Granby Zoological Society Nagoya Aquarium Zoological Gardens The Living Desert Knoxville Zoo National Audubon Society-Research Metropolitan Toronto Zoo Marwell Zoological Park National Geographic Magazine Ranch Sanctuary Minnesota Zoological Garden Milwaukee County Zoo National Zoological Gardens National Aviary in Pittsburgh New York Zoological Society NOAHS Center of South Africa Parco Faunistico "La To:rbiera" Omaha's Henry Doorly Zoo North of Chester Zoological Society Odense Zoo Potter Park Zoo Saint Louis Zoo Oklahoma City Zoo Orana Park Wildlife Trust Racine Zoological Society Sea World, Inc. -
Mammalian Predators Appropriating the Refugia of Their Prey
Mamm Res (2015) 60:285–292 DOI 10.1007/s13364-015-0236-y ORIGINAL PAPER When prey provide more than food: mammalian predators appropriating the refugia of their prey William J. Zielinski 1 Received: 30 September 2014 /Accepted: 20 July 2015 /Published online: 31 July 2015 # Mammal Research Institute, Polish Academy of Sciences, Białowieża, Poland (outside the USA) 2015 Abstract Some mammalian predators acquire both food and predators) may play disproportionately important roles in their shelter from their prey, by eating them and using the refugia communities. the prey construct. I searched the literature for examples of predators that exhibit this behavior and summarize their taxo- Keywords Predator–prey . Dens . Herbivore . Behavior . nomic affiliations, relative sizes, and distributions. I hypothe- Habitat . Resting . Foraging sized that size ratios of species involved in this dynamic would be near 1.0, and that most of these interactions would occur at intermediate and high latitudes. Seventeen species of Introduction Carnivorans exploited at least 23 species of herbivores as food and for their refugia. Most of them (76.4 %) were in the Mammals require food and most require shelter, either to pro- Mustelidae; several small species of canids and a few tect them from predators or from thermal stress. Carnivorous herpestids were exceptions. Surprisingly, the average mammals are unique in that they subsist on mobile food predator/prey weight ratio was 10.51, but few species of pred- sources which, particularly if these sources are vertebrates, ators were more than ten times the weight of the prey whose may build their own refuges to help regulate their body tem- refugia they exploit. -
Cranial Morphological Distinctiveness Between Ursus Arctos and U
East Tennessee State University Digital Commons @ East Tennessee State University Electronic Theses and Dissertations Student Works 5-2017 Cranial Morphological Distinctiveness Between Ursus arctos and U. americanus Benjamin James Hillesheim East Tennessee State University Follow this and additional works at: https://dc.etsu.edu/etd Part of the Biodiversity Commons, Evolution Commons, and the Paleontology Commons Recommended Citation Hillesheim, Benjamin James, "Cranial Morphological Distinctiveness Between Ursus arctos and U. americanus" (2017). Electronic Theses and Dissertations. Paper 3261. https://dc.etsu.edu/etd/3261 This Thesis - Open Access is brought to you for free and open access by the Student Works at Digital Commons @ East Tennessee State University. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Digital Commons @ East Tennessee State University. For more information, please contact [email protected]. Cranial Morphological Distinctiveness Between Ursus arctos and U. americanus ____________________________________ A thesis presented to the Department of Geosciences East Tennessee State University In partial fulfillment of the requirements for the degree Master of Science in Geosciences ____________________________________ by Benjamin Hillesheim May 2017 ____________________________________ Dr. Blaine W. Schubert, Chair Dr. Steven C. Wallace Dr. Josh X. Samuels Keywords: Ursidae, Geometric morphometrics, Ursus americanus, Ursus arctos, Last Glacial Maximum ABSTRACT Cranial Morphological Distinctiveness Between Ursus arctos and U. americanus by Benjamin J. Hillesheim Despite being separated by millions of years of evolution, black bears (Ursus americanus) and brown bears (Ursus arctos) can be difficult to distinguish based on skeletal and dental material alone. Complicating matters, some Late Pleistocene U. americanus are significantly larger in size than their modern relatives, obscuring the identification of the two bears. -
Coyote Canis Latrans in 2007 IUCN Red List (Canis Latrans)
MAMMALS OF MISSISSIPPI 10:1–9 Coyote (Canis latrans) CHRISTOPHER L. MAGEE Department of Wildlife and Fisheries, Mississippi State University, Mississippi State, Mississippi, 39762, USA Abstract—Canis latrans (Say 1823) is a canid commonly called the coyote. It is dog-like in appearance with varied colorations throughout its range. Originally restricted to the western portion of North America, coyotes have expanded across the majority of the continent. Coyotes are omnivorous and extremely adaptable, often populating urban and suburban environments. Preferred habitats include a mixture of forested, open, and brushy areas. Currently, there exist no threats or conservation concerns for the coyote in any part of its range. This species is currently experiencing an increasing population trend. Published 5 December 2008 by the Department of Wildlife and Fisheries, Mississippi State University Coyote location (Jackson 1951; Young 1951; Berg and Canis latrans (Say, 1823) Chesness 1978; Way 2007). The species is sexually dimorphic, with adult females distinctly CONTEXT AND CONTENT. lighter and smaller than adult males (Kennedy Order Carnivora, suborder Caniformia, et al. 2003; Way 2007). Average head and infraorder Cynoidea, family Canidae, subfamily body lengths are about 1.0–1.5 m with a tail Caninae, tribe Canini. Genus Canis consists length of about Young 1951). The skull of the of six species: C. aureus, C. latrans, C. lupus, coyote (Fig. 2) progresses through 6 distinct C. mesomelas, C. simensis, and C. adustus. developmental stages allowing delineation Canis latrans has 19 recognized subspecies between the age classes of juvenile, immature, (Wilson and Reeder 2005). young, young adult, adult, and old adult (Jackson 1951).