A Confirmed Sighting of Pousargues's Mongoose Dologale Dybowskii
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												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. - 
												
												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). - 
												
												South Africa, 2017
WILDWINGS SOUTH AFRICA TOUR Wildwings Davis House MAMMALS AND BIRDS Lodge Causeway th th Bristol BS16 3JB 4 -14 SEPTEMBER 2017 LEADER – RICHARD WEBB +44 01179 658333 www.wildwings.co.uk Leopard INTRODUCTION After the success of the two previous Wildwings’ mammal tours to South Africa in 2016 we set off on the 2017 tour with high expectations and we were not to be disappointed. Despite longer than usual grass at Marrick which made spotlighting more difficult we still managed to find most of the species found on the two tours in 2016 plus a couple of real bonuses. The highlights among the 55 species of mammal seen included: A fantastic encounter with a pack of at least eight African Wild Dogs with seven three-month old puppies, plus another group of three females later the same day. A superb female Leopard on our first afternoon in Madikwe, with an awesome encounter with the same individual in the grounds of our lodge, including one of the clients finding her sitting on his balcony on our last evening! Our best views of Aardwolf to date in Marrick and prolonged views of Aardvark at the same location. Three Brown Hyaenas including one for over 30 minutes one afternoon. Two Black-footed Cats and no fewer than nine (recently-split) African Wildcats including a female with three kittens. 1 Two male Cheetahs and eight or nine Lions. Two Spotted-necked Otters feeding on a fish for over an hour at Warrenton. A superb Black Rhino and over 20 White Rhinos including a boisterous group of nine animals. - 
												
												Chapter 15 the Mammals of Angola
Chapter 15 The Mammals of Angola Pedro Beja, Pedro Vaz Pinto, Luís Veríssimo, Elena Bersacola, Ezequiel Fabiano, Jorge M. Palmeirim, Ara Monadjem, Pedro Monterroso, Magdalena S. Svensson, and Peter John Taylor Abstract Scientific investigations on the mammals of Angola started over 150 years ago, but information remains scarce and scattered, with only one recent published account. Here we provide a synthesis of the mammals of Angola based on a thorough survey of primary and grey literature, as well as recent unpublished records. We present a short history of mammal research, and provide brief information on each species known to occur in the country. Particular attention is given to endemic and near endemic species. We also provide a zoogeographic outline and information on the conservation of Angolan mammals. We found confirmed records for 291 native species, most of which from the orders Rodentia (85), Chiroptera (73), Carnivora (39), and Cetartiodactyla (33). There is a large number of endemic and near endemic species, most of which are rodents or bats. The large diversity of species is favoured by the wide P. Beja (*) CIBIO-InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, Vairão, Portugal CEABN-InBio, Centro de Ecologia Aplicada “Professor Baeta Neves”, Instituto Superior de Agronomia, Universidade de Lisboa, Lisboa, Portugal e-mail: [email protected] P. Vaz Pinto Fundação Kissama, Luanda, Angola CIBIO-InBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, Campus de Vairão, Vairão, Portugal e-mail: [email protected] L. Veríssimo Fundação Kissama, Luanda, Angola e-mail: [email protected] E. - 
												
												List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34. - 
												
												Download Mammal List
SOUTHERN AFRICA MAMMAL LIST, OCTOBER - DECEMBER 2015 Common Name Scientific Name Seen CHIROPTERA Vespertilipnidae Cape bat Neoromicia capensis 1 Pteropodidae Agolan fruit bat Lissonycteris angolensis 1 Hipposideridae Giant Lleaf-nosed bat Hipposideros gigas 1 PRIMATES Cercopithecidae Chacma baboon Papio ursinus 1 Yellow baboon Papio cynocephalus 1 Vervet monkey Chlorocebus pygerythrus 1 Samango monkey Cercopithecus mitis labiatus 1 Galagidae Thick-tailed greater galago Otolemur crassicaudatus 1 Southern lesser galago Galago moholi 1 MACROSCELIDEA Macroscelididae Eastern rock sengi Elephantulus myurus 1 LAGOMORPHA Leporidae Scrub hare Lepus saxatilis 1 Cape hare Lepus capensis 1 Natal red rock hare Pronolagus crassicaudatus 1 RODENTIA Pedetidae Spring hare Pedetes capensis 1 Sciuridae Mutable sun squirrel Heliosciurus mutabilis 1 South African ground squirrel Xerus inauris 1 Congo rope squirrel Funisciurus congicus 1 Ongoye red bush squirrel Paraxerus palliatus ornatus 1 Smith's bush squirrel Paraxerus cepapi 1 Eastern gray squirrel Sciurus carolinensis 1 Muridae Four-striped grass mouse Rhabdomys pumilio 1 Sloggett's vlei rat Otomys sloggetti 1 Petromuridae Dassie rat Petromus typicus 1 CARNIVORA Canidae Bat-eared Fox Otocyon megalotis 1 Black-backed Jackal Canis mesomelas 1 Herpestidae Banded mongoose Mungos mungo 1 Cape gray mongoose Galerella pulverulenta 1 Slender mongoose Galerella sanguinea 1 Common dwarf mongoose Helogale parvula 1 White-tailed mongoose Ichneumia albicauda 1 Yellow mongoose Cynictis penicillata 1 Meerkat Suricata - 
												
												Standards for Feliform Sanctuaries
Global Federation of Animal Sanctuaries Standards For Feliform Sanctuaries Version: June, 2013 ©2012 Global Federation of Animal Sanctuaries Global Federation of Animal Sanctuaries – Standards for Feliform Sanctuaries Table of Contents INTRODUCTION 1 GFAS PRINCIPLES 1 ANIMALS COVERED BY THESE STANDARDS 1 STANDARDS UPDATES 4 FELIFORM STANDARDS 4 FELIFORM HOUSING 4 H-1. Types of Space and Size 4 H-2. Containment 6 H-3. Ground and Plantings 8 H-4. Transfer Doors 9 H-5. Shelter 10 H-6. Enclosure Furniture 12 H-7. Sanitation 13 H-8. Temperature, Humidity, Ventilation, Lighting 14 PHYSICAL FACILITIES AND ADMINISTRATION 16 PF-1. Overall Safety of Facilities 16 PF-2. Water Drainage and Testing 16 PF-3. Life Support 16 PF-4. Hazardous Materials Handling 16 PF-5. Security: Feliform Enclosures 17 PF-6. Perimeter Boundary and Inspections, and Maintenance 18 PF-7. Security: General Safety Monitoring 18 PF-8. Insect and Rodent Control 19 PF-9. Record Keeping 19 PF-10. Animal Transport 20 NUTRITION REQUIREMENTS 21 N-1. Water 21 N-2. Diet 21 N-3. Food Presentation and Feeding Techniques 23 N-4. Food Storage 23 N-5. Food Handling 24 VETERINARY CARE 24 V-1. General Medical Program and Staffing 24 V-2. On-Site and Off-Site Veterinary Facilities 25 V-3. Preventative Medicine Program 25 V-4. Clinical Pathology, Surgical, Treatment and Necropsy Facilities 26 V-5. Quarantine and Isolation of Feliforms 27 i Global Federation of Animal Sanctuaries – Standards for Feliform Sanctuaries V-6. Medical Records and Controlled Substances 28 V-7. Breeding/Contraception 29 V-8. - 
												
												List of Taxa for Which MIL Has Images
LIST OF 27 ORDERS, 163 FAMILIES, 887 GENERA, AND 2064 SPECIES IN MAMMAL IMAGES LIBRARY 31 JULY 2021 AFROSORICIDA (9 genera, 12 species) CHRYSOCHLORIDAE - golden moles 1. Amblysomus hottentotus - Hottentot Golden Mole 2. Chrysospalax villosus - Rough-haired Golden Mole 3. Eremitalpa granti - Grant’s Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus - Lowland Streaked Tenrec 3. Microgale cf. longicaudata - Lesser Long-tailed Shrew Tenrec 4. Microgale cowani - Cowan’s Shrew Tenrec 5. Microgale mergulus - Web-footed Tenrec 6. Nesogale cf. talazaci - Talazac’s Shrew Tenrec 7. Nesogale dobsoni - Dobson’s Shrew Tenrec 8. Setifer setosus - Greater Hedgehog Tenrec 9. Tenrec ecaudatus - Tailless Tenrec ARTIODACTYLA (127 genera, 308 species) ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BALAENIDAE - bowheads and right whales 1. Balaena mysticetus – Bowhead Whale 2. Eubalaena australis - Southern Right Whale 3. Eubalaena glacialis – North Atlantic Right Whale 4. Eubalaena japonica - North Pacific Right 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. Balaenoptera ricei - Rice’s Whale 7. Eschrichtius robustus - Gray Whale 8. Megaptera novaeangliae - Humpback Whale BOVIDAE (54 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Common Impala 3. Aepyceros petersi - Black-faced Impala 4. Alcelaphus caama - Red Hartebeest 5. Alcelaphus cokii - Kongoni (Coke’s Hartebeest) 6. Alcelaphus lelwel - Lelwel Hartebeest 7. Alcelaphus swaynei - Swayne’s Hartebeest 8. Ammelaphus australis - Southern Lesser Kudu 9. Ammelaphus imberbis - Northern Lesser Kudu 10. Ammodorcas clarkei - Dibatag 11. Ammotragus lervia - Aoudad (Barbary Sheep) 12. - 
												
												Captive Care Standards an Overview of Standards for the Keeping of Wild Animals in Captive Care Settings in Malawi the Aap Foundation
CAPTIVE CARE STANDARDS AN OVERVIEW OF STANDARDS FOR THE KEEPING OF WILD ANIMALS IN CAPTIVE CARE SETTINGS IN MALAWI THE AAP FOUNDATION WRITTEN BY ING. J IEPEMA DR. A. SALB ACKNOWLEDGEMENTS These Standards would not have been completed without the support of numerous organisations, stakeholders and individuals. They were produced by Lilongwe Wildlife Trust (LWT) on behalf of the Department of National Parks and Wildlife (DNPW) and the Department of Animal Health and Livestock Development (DAHLD), with financial support from the AAP Foundation and technical input from a working group. Members of the working group included: Mr. W. Mgoola Assistant Director (Research & Development), DNPW Mr. C. M. Manda Deputy Director (Conservation Services), DNPW Dr. J. Nkhoma Animal Health Officer & Focal Point on Wildlife, DAHLD Dr. A. Salb Head of Veterinary Services/Wildlife Emergency Rescue Unit, LWT Ing. J. Iepema Sanctuary Manager, LWT Dr. J. Kazembe Senior Lecturer, Department of Environmental Sciences and Management, LUANAR Mr. E. Zakochera Senior Education Officer, WESM In the process of developing this document, many organisations and individuals from all over the world provided information regarding existing standards for keeping wild animals in captivity. Our thanks go to the Lilongwe Society for the Protection and Care of Animals (LSPCA), the Pan African Sanctuary Alliance (PASA), the Global Federation of Animal Sanctuaries (GFAS), the American Zoo Association (AZA) and the European Associated of Zoos and Aquaria (EAZA). A special thanks goes - 
												
												IIDA, Eriko G.; IDANI, Gen'ichi; OGAWA, Hideshi
MAMMALIAN FAUNA OF THE MIOMBO FOREST IN Title THE UGALLA AREA, WESTERN TANZANIA Author(s) IIDA, Eriko G.; IDANI, Gen'ichi; OGAWA, Hideshi Citation African Study Monographs (2012), 33(4): 253-270 Issue Date 2012-12 URL https://doi.org/10.14989/169670 Right Type Journal Article Textversion publisher Kyoto University African Study Monographs, 33 (4): 253-270, December 2012 253 MAMMALIAN FAUNA OF THE MIOMBO FOREST IN THE UGALLA AREA, WESTERN TANZANIA Eriko G. IIDA Wildlife Research Center of Kyoto University Gen’ichi IDANI Wildlife Research Center of Kyoto University Hideshi OGAWA School of International Liberal Studies, Chukyo University ABSTRACT We collected basic data on the mammalian fauna of the Ugalla area (05°13.0’S, 30°27.5’E), western Tanzania. We identified 50 mammalian species: seven species of Primates; at least one unidentified species of Chiroptera; two identified species of Lagomorpha; four identified species of Rodentia; 17 identified and at least two unidentified species of Carnivora; one species of Tubulidentata; one species of Hyracoidea; and 15 species of Artiodactyla. Nine- teen of these species had not previously been reported from Ugalla. Moreover, eight of these mammal species had not previously been confirmed in this area, according to the Red List of the International World Conservation Union. Ugalla has a diverse mammalian fauna, including species that originated in the tropical rainforest and acacia savanna. In addition, our surveys suggest that genets, African civets, leopards, bush hyraxes and southern reedbucks have differ- ent ecologies from mammals in other regions. Key Words: Mammalian fauna; Miombo forest; Ugalla; Diversity. INTRODUCTION The miombo forest in western Tanzania is located in a region in which the main vegetation changes from tropical rainforest to acacia savanna. - 
												
												A Conϐirmed Sighting of Pousargues's Mongoose Dologale Dybowskii
ϐǯDologale dybowskii Jason WOOLGAR Fig. 1. Pousargues’s Mongoose Dologale dybowskii at Semliki Wildlife Reserve, Uganda, 8 July 2013. I watched at length and photographed a group of Pousargues’s Mongoose Dologale dybowskii on 7 and 8 July 2013 at Semliki Safari Lodge (on the eastern border of Semliki Wildlife Reserve), Uganda. The animals were distinctive in appearance, given my long experience with the main potential confusion species, Common Dwarf Mongoose Helogale parvula. Although the species’s Ǧǡϐ ϐ anywhere in its range for several decades. Keywords: foraging, locality record, reaction to people, Semliki Safari Lodge, sociality, Uganda ϐ±Dologale dybowskii ±± J’ai longuement observé et photographié un groupe de Mangoustes des savanes Dologale dybowskii les 7 et 8 juillet 2013 à Semliki Safari Lodge (sur la frontière orientale de la réserve faunique de Semliki), en Ouganda. Les animaux étaient d’apparence distinctive (compte tenu de ma longue expérience avec la principale espèce qui pourrait potentiellement créer confusion, c’est à dire la Mangouste naine commune Helogale parvula). Bien que la présence de l’espèce était bien connue du personnel de la loge, ° ϐ±±± ǡ ± travers l’ensemble de l’aire de répartition de cette espèce extrêmement mal connue. Pousargues’s Mongoose Dologale dybowskii is known from known as the Toro Game Reserve, Semliki Wildlife Reserve is ͵ͳ ǡ ϐ one of the oldest protected, or at least partly protected, areas of this animal for more than three decades (Aebsicher et al. in Uganda and occupies - 
											
Why Does Natural Home Range Size Predict Captive Carnivora Welfare?
Why does Natural Home Range Size Predict Captive Carnivora Welfare? by Miranda Bandeli A Thesis presented to The University of Guelph In partial fulfilment of requirements for the degree of Master of Science in Animal Biosciences Guelph, Ontario, Canada © Miranda Bandeli, May, 2018 ABSTRACT WHY DOES NATURAL HOME RANGE SIZE PREDICT CAPTIVE CARNIVORA WELFARE? Miranda Bandeli Advisor(s): University of Guelph, 2018 Dr. Georgia Mason Natural ranging behaviours were investigated as risk factors for stereotypic behaviour (SB) and infant mortality (CIM) in captive Carnivora. Data collected via literature searches were added into previously created databases. Species-typical median home range size predicted stereotypic route-tracing, but not total SB or CIM. I then assessed whether any correlates of range size proved better predictors of route-tracing. No correlates statistically eliminated the effect of range size, but two greatly increased the R2 when combined with range size: wide-ranging species that are also not predated and travel a small proportion of their annual distance daily spent the most time route-tracing. Additionally, ranging flexibility proved important: species with large home ranges that also have little variability in their range sizes spent the most time route-tracing. However, since the effect of home range size on route-tracing was not explained by any correlate tested, home range size may be intrinsically important. ACKNOWLEDGEMENTS First, I would like to thank my advisor Georgia Mason for finding me a project that perfectly aligned with my interests and skills. Thank you also for all your guidance and support throughout my time at Guelph and helping me grow as a researcher.