Small Carnivore Conservation Action Plan
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A Fire Baseline for Tanzania
Sustainable Forest Management in a Changing Climate FAO‐Finland Forestry Programme – TANZANIA A Fire Baseline for Tanzania Dar es Salaam 2013 Executive Summary In Tanzania wild fires are reported to be increasing at an alarming rate. The problem of wildfires in Tanzania is complex and should not be addressed on a sectoral level as it concerns all the aspects related to forest and land management, prevention, suppression, and post‐fire management. It is a problem of general policy, land policy and forest policy and legislation, as much as it is a problem of equipment and capacity building within any one sector. Despite the magnitude of threat suggested, hard data on the number and extent of wildfires are lacking, most statements on the wildfire issue are based on story and opinions (Madoffe et al., 2005). Wildfires are considered to be a ‘problem’. However, the data and information to describe the extent, nature, impacts and source of wildfires have not been compiled and analyzed; this is a Fire Baseline, which is the subject of the work reported here. The main objective of this study was to elaborate “Tanzanian wildfire baseline information”, as the starting point for a Fire Information System. The step taken in compiling this fire baseline for Tanzania is a sound strategic one and should be something that is repeated in most countries that are working to understand and account for fires in their landscapes. In the preparation of the Fire Baseline there have been a series of aspects that have been indentified, which can provide a set of ongoing analyses to further refine and contribute to enhancing the insights and understanding of fire in Tanzania. -
The Gut Microbiota of the Egyptian Mongoose As an Early Warning Indicator of Ecosystem Health in Portugal
International Journal of Environmental Research and Public Health Article The Gut Microbiota of the Egyptian Mongoose as an Early Warning Indicator of Ecosystem Health in Portugal Mónica V. Cunha 1,2,3,* , Teresa Albuquerque 1, Patrícia Themudo 1, Carlos Fonseca 4, Victor Bandeira 4 and Luís M. Rosalino 2,4 1 National Institute for Agrarian and Veterinary Research (INIAV, IP), Wildlife, Hunting and Biodiversity R&D Unit, 2780-157 Oeiras, Portugal; [email protected] (T.A.); [email protected] (P.T.) 2 Centre for Ecology, Evolution and Environmental Changes (cE3c), Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisboa, Portugal; [email protected] 3 Biosystems & Integrative Sciences Institute (BioISI), Faculdade de Ciências da Universidade de Lisboa, 1749-016 Lisboa, Portugal 4 Departamento de Biologia & CESAM, Universidade de Aveiro, 3810-193 Aveiro, Portugal; [email protected] (C.F.); [email protected] (V.B.) * Correspondence: [email protected]; Tel.: +351-214-403-500 Received: 1 April 2020; Accepted: 27 April 2020; Published: 29 April 2020 Abstract: The Egyptian mongoose is a carnivore mammal species that in the last decades experienced a tremendous expansion in Iberia, particularly in Portugal, mainly due to its remarkable ecological plasticity in response to land-use changes. However, this species may have a disruptive role on native communities in areas where it has recently arrived due to predation and the potential introduction of novel pathogens. We report reference information on the cultivable gut microbial landscape of widely distributed Egyptian mongoose populations (Herpestes ichneumon, n = 53) and related antimicrobial tolerance across environmental gradients. -
Helogale Parvula)
Vocal Recruitment in Dwarf Mongooses (Helogale parvula) Janneke Rubow Thesis presented in fulfilment of the requirements for the degree of Master of Science in the Faculty of Science at Stellenbosch University Supervisor: Prof. Michael I. Cherry Co-supervisor: Dr. Lynda L. Sharpe March 2017 Stellenbosch University https://scholar.sun.ac.za DECLARATION By submitting this thesis electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the sole author thereof (save to the extent explicitly otherwise stated), that reproduction and publication thereof by Stellenbosch University will not infringe any third party rights and that I have not previously in its entirety or in part submitted it for obtaining any qualification. Janneke Rubow, March 2017 Copyright © 2017 Stellenbosch University All rights reserved Stellenbosch University https://scholar.sun.ac.za Abstract Vocal communication is important in social vertebrates, particularly those for whom dense vegetation obscures visual signals. Vocal signals often convey secondary information to facilitate rapid and appropriate responses. This function is vital in long-distance communication. The long-distance recruitment vocalisations of dwarf mongooses (Helogale parvula) provide an ideal opportunity to study informative cues in acoustic communication. This study examined the information conveyed by two recruitment calls given in snake encounter and isolation contexts, and whether dwarf mongooses are able to respond differently on the basis of these cues. Vocalisations were collected opportunistically from four wild groups of dwarf mongooses. The acoustic parameters of recruitment calls were then analysed for distinction between contexts within recruitment calls in general, distinction within isolation calls between groups, sexes and individuals, and the individuality of recruitment calls in comparison to dwarf mongoose contact calls. -
The Yellow Mongoose Cynictis Penicillata in the Great Fish River Reserve (Eastern Cape, South Africa)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by South East Academic Libraries System (SEALS) Spatio-temporal ecology of the yellow mongoose Cynictis penicillata in the Great Fish River Reserve (Eastern Cape, South Africa) By Owen Akhona Mbatyoti A dissertation submitted in fulfilment of the requirements for the degree of MASTER OF SCIENCE (ZOOLOGY) in the Faculty of Science and Agriculture at the University of Fort Hare August 2012 Supervisor: Dr Emmanuel Do Linh San DECLARATION 1. This is to declare that this dissertation entitled “Spatio-temporal ecology of the yellow mongoose Cynictis penicillata in the Great Fish River Reserve (Eastern Cape, South Africa)” is my own work and has not been previously submitted to another institute. 2. I know that plagiarism means taking and using the ideas, writings, work or inventions of another person as if they were one’s own. I know that plagiarism not only includes verbatim copying, but also extensive use of another person’s ideas without proper acknowledgement (which sometimes includes the use of quotation marks). I know that plagiarism covers this sort of material found in textual sources (e.g. books, journal articles and scientific reports) and from the Internet. 3. I acknowledge and understand that plagiarism is wrong. 4. I understand that my research must be accurately referenced. I have followed the academic rules and conventions concerning referencing, citation and the use of quotations. 5. I have not allowed, nor will I in the future allow, anyone to copy my work with the intention of passing it off as their own work. -
VOLATILE COMPOUNDS from ANAL GLANDS of the WOLVERINE, Gulo Gulo
Journal of Chemical Ecology, Vol. 12, No. 9, September 2005 ( #2005) DOI: 10.1007/s10886-005-6080-9 VOLATILE COMPOUNDS FROM ANAL GLANDS OF THE WOLVERINE, Gulo gulo WILLIAM F. WOOD,1,* MIRANDA N. TERWILLIGER,2 and JEFFREY P. COPELAND3 1Department of Chemistry, Humboldt State University, Arcata, CA 95521, USA 2Alaska Cooperative Fish & Wildlife Research Unit, Department of Biology & Wildlife, University of Alaska, Fairbanks, AK 99775, USA 3USDA Forest Service, Rocky Mountain Research Station, Missoula, MT 59801, USA (Received February 12, 2005; revised March 24, 2005; accepted April 20, 2005) Abstract—Dichloromethane extracts of wolverine (Gulo gulo, Mustelinae, Mustelidae) anal gland secretion were examined by gas chromatographyYmass spectrometry. The secretion composition was complex and variable for the six samples examined: 123 compounds were detected in total, with the number per animal ranging from 45 to 71 compounds. Only six compounds were common to all extracts: 3-methylbutanoic acid, 2-methylbutanoic acid, phenylacetic acid, a-tocopherol, cholesterol, and a compound tentatively identified as 2-methyldecanoic acid. The highly odoriferous thietanes and dithiolanes found in anal gland secretions of some members of the Mustelinae [ferrets, mink, stoats, and weasels (Mustela spp.) and zorillas (Ictonyx spp.)] were not observed. The composition of the wolverine’s anal gland secretion is similar to that of two other members of the Mustelinae, the pine and beech marten (Martes spp.). Key WordsVWolverine, Gulo gulo, Mustelinae, Mustelidae, scent marking, fear-defense mechanism, short-chain carboxylic acids. INTRODUCTION The wolverine (Gulo gulo) is the largest terrestrial member of the Mustelidae and is part of the subfamily, Mustelinae, which includes ferrets, fishers, martens, mink, stoats, weasels, and zorillas. -
Felis Silvestris, Wild Cat
The IUCN Red List of Threatened Species™ ISSN 2307-8235 (online) IUCN 2008: T60354712A50652361 Felis silvestris, Wild Cat Assessment by: Yamaguchi, N., Kitchener, A., Driscoll, C. & Nussberger, B. View on www.iucnredlist.org Citation: Yamaguchi, N., Kitchener, A., Driscoll, C. & Nussberger, B. 2015. Felis silvestris. The IUCN Red List of Threatened Species 2015: e.T60354712A50652361. http://dx.doi.org/10.2305/IUCN.UK.2015-2.RLTS.T60354712A50652361.en Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale, reposting or other commercial purposes is prohibited without prior written permission from the copyright holder. For further details see Terms of Use. The IUCN Red List of Threatened Species™ is produced and managed by the IUCN Global Species Programme, the IUCN Species Survival Commission (SSC) and The IUCN Red List Partnership. The IUCN Red List Partners are: BirdLife International; Botanic Gardens Conservation International; Conservation International; Microsoft; NatureServe; Royal Botanic Gardens, Kew; Sapienza University of Rome; Texas A&M University; Wildscreen; and Zoological Society of London. If you see any errors or have any questions or suggestions on what is shown in this document, please provide us with feedback so that we can correct or extend the information -
CHAPTER 1: Introduction 1
University of Pretoria etd, Wilson K A (2006) Status and distribution of cheetah outside formal conservation areas in the Thabazimbi district, Limpopo province by Kelly-Anne Wilson Submitted in partial fulfilment for the requirements for the degree Magister Scientiae in Wildlife Management Centre for Wildlife Management Faculty of Natural and Agricultural Sciences University of Pretoria Pretoria Supervisor: Prof. J. du P. Bothma Co-supervisor: Prof. G. H. Verdoorn February 2006 University of Pretoria etd, Wilson K A (2006) STATUS AND DISTRIBUTION OF CHEETAH OUTSIDE FORMAL CONSERVATION AREAS IN THE THABAZIMBI DISTRICT, LIMPOPO PROVINCE by Kelly-Anne Wilson Supervisor: Prof. Dr. J. du P. Bothma Co-supervisor: Prof. Dr. G. H. Verdoorn Centre for Wildlife Management Faculty of Natural and Agricultural Sciences University of Pretoria Magister Scientiae (Wildlife Management) ABSTRACT The current status of the cheetah Acinonyx jubatus outside formal conservation areas in South Africa is undetermined. The largest part of the cheetah population in South Africa occurs on cattle and wildlife ranches. Conflict between cheetahs and landowners is common and cheetahs are often persecuted. Cheetah management and conservation efforts are hampered as little data are available on the free-roaming cheetah population. A questionnaire survey was done in the Thabazimbi district of the Limpopo province to collect data on the status and distribution of cheetahs in the district and on the ranching practices and attitudes of landowners. By using this method, a population estimate of 42 – 63 cheetahs was obtained. Camera trapping was done at a scent-marking post to investigate the marking behaviour of cheetahs. Seven different cheetahs were identified marking at one specific tree. -
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. -
African Wildcat 1 African Wildcat
African Wildcat 1 African Wildcat African Wildcat[1] Scientific classification Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Carnivora Family: Felidae Genus: Felis Species: F. silvestris Subspecies: F. s. lybica Trinomial name Felis silvestris lybica Forster, 1770 The African wildcat (Felis silvestris lybica), also known as the desert cat, and Vaalboskat (Vaal-forest-cat) in Afrikaans, is a subspecies of the wildcat (F. silvestris). They appear to have diverged from the other subspecies about 131,000 years ago.[2] Some individual F. s. lybica were first domesticated about 10,000 years ago in the Middle East, and are among the ancestors of the domestic cat. Remains of domesticated cats have been included in human burials as far back as 9,500 years ago in Cyprus.[3] [4] Physical characteristics The African wildcat is sandy brown to yellow-grey in color, with black stripes on the tail. The fur is shorter than that of the European subspecies. It is also considerably smaller: the head-body length is 45 to 75 cm (17.7 to 29.5 inches), the tail 20 to 38 cm (7.87 to 15 inches), and the weight ranges from 3 to 6.5 kg (6.61 to 14.3 lbs). Distribution and habitat The African wildcat is found in Africa and in the Middle East, in a wide range of habitats: steppes, savannas and bushland. The sand cat (Felis margarita) is the species found in even more arid areas. Skull African Wildcat 2 Behaviour The African wildcat eats primarily mice, rats and other small mammals. When the opportunity arises, it also eats birds, reptiles, amphibians, and insects. -
Civettictis Civetta (Schreber, 1776)
Civettictis civetta (Schreber, 1776) The African civet, Civettictis civetta is native to and widely distributed in Africa. It was probably introduced to Sao Tome & Principe with the weasel Mustela nivalis to control rodents. African civets occupy a range of habitats including secondary forest, woodland, bush habitats as well as aquatic habitats. They are not common in interior forest habitats but thrive in degraded and deforested areas. They have been recorded at altitudes up to 5000 m asl on Mt Kilimanjaro The Guinea Lidless Skink (Afroablepharus africana) is classified as ‘Vulnerable (VU)’ in the IUCN Red List of Threatened Species. It is restricted to three locations on the islands of Sâo Tomé, Principé, and Rolas in the Gulf of Guinea. The main threats to this species are suspected to be loss of habitat through deforestation and predation Photo credit: Brianna Hackler by introduced mammals. Introduced mammals on these islands include the African civet, Norway rat (Rattus bocagei); the Sao Tome Canary (Neospiza concolor) and the norvegicus) ship rat (Rattus rattus), House mouse (Mus Sao Tome Fiscal (Lanius newtoni) are under threat of loss musculus), Mona monkey (Cercopithecus mona) and of habitat and potential predation by introduced mammals weasel. that include the African civet, ship rat, house mouse, Mona Declining populations of three endemic and ‘Critically monkey and weasel. Feral pigs (Sus scrofa) are also present Endangered (CR)’ birds the Sao Tome Ibis (Bostrychia and could be a threat. References: IUCN 2011. IUCN Red List of Threatened Species. Version 2011.2 ISSG 2012. Global Invasive Species Database Click here to view archives of previous weeks’ species. -
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. -
Monitoring Wolverines in Northeast Oregon
Monitoring Wolverines in Northeast Oregon January 2011 – December 2012 Final Report Authors: Audrey J. Magoun Patrick Valkenburg Clinton D. Long Judy K. Long Submitted to: The Wolverine Foundation, Inc. February 2013 Cite as: A. J. Magoun, P. Valkenburg, C. D. Long, and J. K. Long. 2013. Monitoring wolverines in northeast Oregon. January 2011 – December 2012. Final Report. The Wolverine Foundation, Inc., Kuna, Idaho. [http://wolverinefoundation.org/] Copies of this report are available from: The Wolverine Foundation, Inc. [http://wolverinefoundation.org/] Oregon Department of Fish and Wildlife [http://www.dfw.state.or.us/conservationstrategy/publications.asp] Oregon Wildlife Heritage Foundation [http://www.owhf.org/] U. S. Forest Service [http://www.fs.usda.gov/land/wallowa-whitman/landmanagement] Major Funding and Logistical Support The Wolverine Foundation, Inc. Oregon Department of Fish and Wildlife Oregon Wildlife Heritage Foundation U. S. Forest Service U. S. Fish and Wildlife Service Wolverine Discovery Center Norcross Wildlife Foundation Seattle Foundation Wildlife Conservation Society National Park Service 2 Special thanks to everyone who provided contributions, assistance, and observations of wolverines in the Wallowa-Whitman National Forest and other areas in Oregon. We appreciate all the help and interest of the staffs of the Oregon Department of Fish and Wildlife, Oregon Wildlife Heritage Foundation, U. S. Forest Service, U. S. Fish and Wildlife Service, Wildlife Conservation Society, and the National Park Service. We also thank the following individuals for their assistance with the field work: Jim Akenson, Holly Akenson, Malin Aronsson, Norma Biggar, Ken Bronec, Steve Bronson, Roblyn Brown, Vic Coggins, Alex Coutant, Cliff Crego, Leonard Erickson, Bjorn Hansen, Mike Hansen, Hans Hayden, Tim Hiller, Janet Hohmann, Pat Matthews, David McCullough, Glenn McDonald, Jamie McFadden, Kendrick Moholt, Mark Penninger, Jens Persson, Lynne Price, Brian Ratliff, Jamie Ratliff, John Stephenson, John Wyanens, Rebecca Watters, Russ Westlake, and Jeff Yanke.