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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: -
Pantanal, Brazil 12Th July to 20Th July 2015
Pantanal, Brazil 12th July to 20th July 2015 Steve Firth Catherine Griffiths This trip was an attempt to see some mammal species that had eluded us on many previous visits to South America. Cats were the main focus, specifically Jaguar and Ocelot, and we were hoping for Giant Anteater as a bonus. When we started planning the trip some ten months in advance, the exchange rate was £1 = R$3.8. The pound strengthened considerably in the intervening period and was £1 = R$5.0 during the visit. This helped to appreciably reduce costs . We flew from London to Campo Grande via Sao Paulo with TAM. There was a 10 hour stopover, but the flight was a great deal cheaper than any offered by other Airlines. On the return leg we flew from Cuiaba to London again via Sao Paulo, again with a long layover. The total Cost per person was £943.35. TAM proved to be more efficient than we had expected (we had had a few memorable difficulties with VARIG 15 years previously) and can be recommended. The Campo Grande to Cuiaba leg was flown with AZUL, booked via their website. The rate quoted, R$546.50 (£70.84 each at the time of booking) for two people, was actually charged to our credit card as US Dollars $546.50. This was noticed immediately and after a call to AZUL in Brazil, they swiftly refunded the first charge and debited the correct amount. AZUL are a low cost carrier, but this was not reflected in their service or punctuality. -
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. -
Chinese Mountain Cat 1 Chinese Mountain Cat
Chinese mountain cat 1 Chinese mountain cat Chinese Mountain Cat[1] Conservation status [2] Vulnerable (IUCN 3.1) Scientific classification Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Carnivora Family: Felidae Genus: Felis Species: F. bieti Binomial name Felis bieti Milne-Edwards, 1892 Distribution of the Chinese Mountain Cat (in green) The Chinese Mountain Cat (Felis bieti), also known as the Chinese Desert Cat, is a small wild cat of western China. It is the least known member of the genus Felis, the common cats. A 2007 DNA study found that it is a subspecies of Felis silvestris; should the scientific community accept this result, this cat would be reclassified as Felis silvestris bieti.[3] Some authorities regard the chutuchta and vellerosa subspecies of the Wildcat as Chinese Mountain Cat subspecies.[1] Chinese mountain cat 2 Description Except for the colour of its fur, this cat resembles a European Wildcat in its physical appearance. It is 27–33 in (69–84 cm) long, plus a 11.5–16 in (29–41 cm) tail. The adult weight can range from 6.5 to 9 kilograms (14 to 20 lb). They have a relatively broad skull, and long hair growing between the pads of their feet.[4] The fur is sand-coloured with dark guard hairs; the underside is whitish, legs and tail bear black rings. In addition there are faint dark horizontal stripes on the face and legs, which may be hardly visible. The ears and tail have black tips, and there are also a few dark bands on the tail.[4] Distribution and ecology The Chinese Mountain Cat is endemic to China and has a limited distribution over the northeastern parts of the Tibetan Plateau in Qinghai and northern Sichuan.[5] It inhabits sparsely-wooded forests and shrublands,[4] and is occasionally found in true deserts. -
The Leopardus Tigrinus Is One of the Smallest Wild Cats in South America; and the Smallest Cat in Brazil (Oliveira-Santos Et Al
Mckenzie Brocker Conservation Biology David Stokes 20 February 2014 Leopardus Tigrinus Description: The Leopardus tigrinus is one of the smallest wild cats in South America; and the smallest cat in Brazil (Oliveira-Santos et al. 2012). L. tigrinus is roughly the size of a domestic house cat, with its weight ranging from 1.8-3.4 kg (Silva-Pereira 2010). The average body length is 710 millimeters and the cat’s tail is roughly one-third of its body length averaging 250 millimeters in length. Males tend to be slightly larger than the females (Gardner 1971). The species’ coat is of a yellowish-brown or ochre coloration patterned prominently with open rosettes (Trigo et al. 2013). Cases of melanism, or dark pigmentation, have been reported but are not as common (Oliveira-Santos et al 2012). These characteristics spots are what give the L. tigrinus its common names of little spotted cat, little tiger cat, tigrina, tigrillo, and oncilla. The names tigrillo, little tiger cat, and little spotted cat are sometimes used interchangeably with other small Neotropical cats species which can lead to confusion. The species is closely related to other feline species with overlapping habitat areas and similar colorations; namely, the ocelot, Leopardus pardalis, the margay, Leopardus weidii, Geoffroys cat, Leopardus geoffroyi, and the pampas cat, Leopardus colocolo (Trigo et al. 2013). Distribution: The L. tigrinus is reported to have a wide distribution from as far north as Costa Rica to as far south as Northern Argentina. However, its exact distribution is still under study, as there have been few reports of occurrences in Central America. -
Panthera Onca) Distribution, Density, and Movement in the Brazilian Pantanal
SUNY College of Environmental Science and Forestry Digital Commons @ ESF Dissertations and Theses 6-10-2019 Drivers of jaguar (Panthera onca) distribution, density, and movement in the Brazilian Pantanal Allison Devlin [email protected] Follow this and additional works at: https://digitalcommons.esf.edu/etds Part of the Environmental Monitoring Commons, and the Natural Resources and Conservation Commons Recommended Citation Devlin, Allison, "Drivers of jaguar (Panthera onca) distribution, density, and movement in the Brazilian Pantanal" (2019). Dissertations and Theses. 114. https://digitalcommons.esf.edu/etds/114 This Open Access Dissertation is brought to you for free and open access by Digital Commons @ ESF. It has been accepted for inclusion in Dissertations and Theses by an authorized administrator of Digital Commons @ ESF. For more information, please contact [email protected], [email protected]. DRIVERS OF JAGUAR (PANTHERA ONCA) DISTRIBUTION, DENSITY, AND MOVEMENT IN THE BRAZILIAN PANTANAL by Allison Loretta Devlin A thesis submitted in partial fulfillment of the requirements for the Doctor of Philosophy Degree State University of New York College of Environmental Science and Forestry Syracuse, New York June 2019 Department of Environmental and Forest Biology Approved by: Jacqueline L. Frair, Major Professor Stephen V. Stehman, Chair, Examining Committee James P. Gibbs, Examining Committee Jonathan B. Cohen, Examining Committee Peter G. Crawshaw Jr., Examining Committee Luke T.B. Hunter, Examining Committee Melissa K. Fierke, Department Chair S. Scott Shannon, Dean, The Graduate School © 2019 Copyright A.L. Devlin All rights reserved Acknowledgements I am indebted to many mentors, colleagues, friends, and loved ones whose guidance, support, patience, and constructive challenges have carried this project to its culmination. -
1 the Origin and Evolution of the Domestic Cat
1 The Origin and Evolution of the Domestic Cat There are approximately 40 different species of the cat family, classification Felidae (Table 1.1), all of which are descended from a leopard-like predator Pseudaelurus that existed in South-east Asia around 11 million years ago (O’Brien and Johnson, 2007). Other than the domestic cat, the most well known of the Felidae are the big cats such as lions, tigers and panthers, sub-classification Panthera. But the cat family also includes a large number of small cats, including a group commonly known as the wildcats, sub-classification Felis silvestris (Table 1.2). Physical similarity suggests that the domestic cat (Felis silvestris catus) originally derived from one or more than one of these small wildcats. DNA examination shows that it is most closely related to the African wildcat (Felis silvestris lybica), which has almost identical DNA, indicating that the African wildcat is the domestic cat’s primary ancestor (Lipinski et al., 2008). The African Wildcat The African wildcat is still in existence today and is a solitary and highly territorial animal indigenous to areas of North Africa and the Near East, the region where domestication of the cat is believed to have first taken place (Driscoll et al., 2007; Faure and Kitchener, 2009). It is primarily a nocturnal hunter that preys mainly on rodents but it will also eat insects, reptiles and other mammals including the young of small antelopes. Also known as the Arabian or North African wildcat, it is similar in appearance to a domestic tabby, with a striped grey/sandy-coloured coat, but is slightly larger and with longer legs (Fig. -
Threats from Human Land Use and Climate Change to the Kodkod Leopardus Guigna
Assessing the distribution of a Vulnerable felid species: threats from human land use and climate change to the kodkod Leopardus guigna G RIET A.E. CUYCKENS,MIRIAM M. MORALES and M ARCELO F. TOGNELLI Abstract Climate change and habitat fragmentation are Introduction considered key pressures on biodiversity, and mammalian carnivores with a limited geographical distribution are limate change and destruction of natural habitats particularly vulnerable. The kodkod Leopardus guigna,a Cthrough human activities are major threats to terres- small felid endemic to the temperate forests of southern trial biodiversity. These pressures have led to substantial ’ Chile and Argentina, has the smallest geographical range range contractions and species extinctions (Parmesan & 2003 2003 2004 of any New World felid. Although the species occurs in Yohe, ; Root et al., ; Opdam & Wascher, ), 2008 protected areas in both countries, it is not known how well including for mammals (Schipper et al., ), and species 1991 these areas protect the kodkod either currently or under at high altitudes are particularly vulnerable (Innes, ; 1997 2003 climate change scenarios. We used species distribution Diaz & Bradley, ; Burns et al., ; Thomas et al., 2004 models and spatial analyses to assess the distribution of the ). Knowledge of the geographical distribution of species 2000 kodkod, examining the effects of changes in human land use is essential to assess these threats (Regan et al., ; Conrad 2006 and future climate change. We also assessed the species’ et al., ) but data on the distribution of rare species is 2006 2009 present representation in protected areas and in light of limited (Hernandez et al., ; Thorn et al., ). -
Lynx, Felis Lynx, Predation on Red Foxes, Vulpes Vulpes, Caribou
Lynx, Fe/is lynx, predation on Red Foxes, Vulpes vulpes, Caribou, Rangifer tarandus, and Dall Sheep, Ovis dalli, in Alaska ROBERT 0. STEPHENSON, 1 DANIEL V. GRANGAARD,2 and JOHN BURCH3 1Alaska Department of Fish and Game, 1300 College Road, Fairbanks, Alaska, 99701 2Alaska Department of Fish and Game, P.O. Box 305, Tok, Alaska 99780 JNational Park Service, P.O. Box 9, Denali National Park, Alaska 99755 Stephenson, Robert 0., Daniel Y. Grangaard, and John Burch. 1991. Lynx, Fe/is lynx, predation on Red Foxes, Vulpes vulpes, Caribou, Rangifer tarandus, and Dall Sheep, Ovis dalli, in Alaska. Canadian Field-Naturalist 105(2): 255- 262. Observations of Canada Lynx (Fe/is lynx) predation on Red Foxes ( Vulpes vulpes) and medium-sized ungulates during winter are reviewed. Characteristics of I 3 successful attacks on Red Foxes and 16 cases of predation on Caribou (Rangifer tarandus) and Dall Sheep (Ovis dalli) suggest that Lynx are capable of killing even adults of these species, with foxes being killed most easily. The occurrence of Lynx predation on these relatively large prey appears to be greatest when Snowshoe Hares (Lepus americanus) are scarce. Key Words: Canada Lynx, Fe/is lynx, Red Fox, Vulpes vulpes, Caribou, Rangifer tarandus, Dall Sheep, Ovis dalli, predation, Alaska. Although the European Lynx (Felis lynx lynx) quently reach 25° C in summer and -10 to -40° C in regularly kills large prey (Haglund 1966; Pullianen winter. Snow depths are generally below 80 cm, 1981), the Canada Lynx (Felis lynx canadensis) and snow usually remains loosely packed except at relies largely on small game, primarily Snowshoe high elevations. -
Apr/May/June 2017 • Volume 61 Issue 2 TABLE OF
Apr/May/June 2017 • Volume 61 Issue 2 TABLE OF APRIL - JUNE 2017 | VOLUME 61, ISSUE 2 cc oo nn tt ee nn tt ss Features Designing Gibs’s Outdoor Enclosure 6 Danny Waldo’s patio pergola-inspired bobcat habitat. 2016 FCF Big Cat Census 8 Kevin Chambers updates the numbers on cats in U.S. captivity. 2222 In Memory: A Tribute to Sally, African Caracal 12 (November 28, 1998 – December 2, 2016) Billie Lambert shares memories of a very special caracal. An Eye For An Eye: Tapanga’s Story 16 Sheri DeFlorio didn’t give up and saved Tapanga’s eyesight. Convention Update 22 July 25 through 27 – Sarasota Florida – don’t miss it! Zandy’s Litter of Seven 26 Mechel Whitaker has a scientific approach to nutrition and husbandry. MaxAMillion was Truly One in a Million 30 Debbie Hayes remembers 18 years of bobcat love. Starla the Geoffroy’s Cat 33 Tina Rochester shares her loss in hopes it will save another life. Acupuncture for Ataxia 35 Shelleen Mathews gave this unconventional treatment a try. Wildlife Conservation Network Spring Expo 38 Chris Tromborg and Lynette Lyon represented the FCF. 3333 66 2525 Feline Conservation Federation Volume 61, Issue 2 • Apr.-June 2017 JOIN THE FCF IN ITS CONSERVATION EFFORTS - WWW.FELINECONSERVATION.ORG The FCF supports conservation of wild felids by advocating for qualified individuals to own and to pursue hus- bandry of wild felines, providing expertise and material support to ensure the continued welfare and viability of these populations, contributing to research, and funding protection programs that benefit felids living in nature. -
PICA Project Report (Action A2.2 & 2.3)
PICA Project Report (Action A2.2 & 2.3) Investigation of Pallas’s cat activity patterns and temporal interactions with sympatric species Authors: Katarzyna Ruta, Gustaf Samelius, David Barclay, Emma Nygren PICA - “Conservation of the Pallas’s cat through capacity building, research, and global planning” 1. Introduction: 1.1 Activity patterns of wild felids: Activity patterns form a part of species’ adaptation to their environment (Beltran & Delibes, 1994) and are therefore a fundamental aspect of animal behaviour (Nielsen, 1983; Weller & Bennett, 2001). Felids are generally considered to be crepuscular and nocturnal in their activity (Kitchener, 1991), although they are well adapted to function in a wide range of light conditions (Sunquist & Sunquist, 2002). Numerous abiotic pressures and biotic interactions are known to shape the temporal behaviour of (cat-like) carnivores (Marinho et al., 2018), including changes in temperature (Beltran & Delibes, 1994; Podolski et al., 2013), light (Huck et al., 2017; Heurich et al., 2014) and season (Podolski et al., 2013; Manfredi et al., 2011), sex and reproductive status of the animal (Kolbe & Squires, 2007; Schmidt, 1999; Schmidt et al., 2009), predation risk (Caro, 2005; Farías et al., 2012) and human disturbance (Wolf & Ale, 2009; Ale & Brown, 2009). Owing to the dietary constraints of carnivores whose preys have their own well-defined circadian rhythms (Halle, 2000; Zielinski, 2000), the availability and vulnerability of prey is, however, considered as one of the main influences on predator temporal activity (Zielinski, 1988; Lodé, 1995). According to Optimal Foraging Theory, predators are expected to synchronize their daily activity with the activity of their most profitable prey, increasing the probability of encounters while reducing energy expenditure (MacArthur & Pianka, 1966; Monterroso et al., 2013; Emmons, 1987). -
Origin of the Egyptian Domestic Cat
UPTEC X 12 012 Examensarbete 30 hp Juni 2012 Origin of the Egyptian Domestic Cat Carolin Johansson Molecular Biotechnology Programme Uppsala University School of Engineering UPTEC X 12 012 Date of issue 2012-06 Author Carolin Johansson Title (English) Origin of the Egyptian Domestic Cat Title (Swedish) Abstract This study presents mitochondrial genome sequences from 22 Egyptian house cats with the aim of resolving the uncertain origin of the contemporary world-wide population of Domestic cats. Together with data from earlier studies it has been possible to confirm some of the previously suggested haplotype identifications and phylogeny of the Domestic cat lineage. Moreover, by applying a molecular clock, it is proposed that the Domestic cat lineage has experienced several expansions representing domestication and/or breeding in pre-historical and historical times, seemingly in concordance with theories of a domestication origin in the Neolithic Middle East and in Pharaonic Egypt. In addition, the present study also demonstrates the possibility of retrieving long polynucleotide sequences from hair shafts and a time-efficient way to amplify a complete feline mitochondrial genome. Keywords Feline domestication, cat in ancient Egypt, mitochondrial genome, Felis silvestris libyca Supervisors Anders Götherström Uppsala University Scientific reviewer Jan Storå Stockholm University Project name Sponsors Language Security English Classification ISSN 1401-2138 Supplementary bibliographical information Pages 123 Biology Education Centre Biomedical Center Husargatan 3 Uppsala Box 592 S-75124 Uppsala Tel +46 (0)18 4710000 Fax +46 (0)18 471 4687 Origin of the Egyptian Domestic Cat Carolin Johansson Populärvetenskaplig sammanfattning Det är inte sedan tidigare känt exakt hur, när och var tamkatten domesticerades.