DRAFT SPECIES MANAGEMENT PLAN Roan Antelope Sable Antelope Tsessebe
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Damaliscus Pygargus Phillipsi – Blesbok
Damaliscus pygargus phillipsi – Blesbok colour pattern (Fabricius et al. 1989). Hybridisation between these taxa threatens the genetic integrity of both subspecies (Skinner & Chimimba 2005). Assessment Rationale Listed as Least Concern, as Blesbok are abundant on both formally and privately protected land. We estimate a minimum mature population size of 54,426 individuals (using a 70% mature population structure) across 678 protected areas and wildlife ranches (counts between 2010 and 2016). There are at least an estimated 17,235 animals (counts between 2013 and 2016) on formally Emmanuel Do Linh San protected areas across the country, with the largest subpopulation occurring on Golden Gate Highlands National Park. The population has increased significantly Regional Red List status (2016) Least Concern over three generations (1990–2015) in formally protected National Red List status (2004) Least Concern areas across its range and is similarly suspected to have increased on private lands. Apart from hybridisation with Reasons for change No change Bontebok, there are currently no major threats to its long- Global Red List status (2008) Least Concern term survival. Approximately 69% of Blesbok can be considered genetically pure (A. van Wyk & D. Dalton TOPS listing (NEMBA) None unpubl. data), and stricter translocation policies should be CITES listing None established to prevent the mixing of subspecies. Overall, this subspecies could become a keystone in the Endemic Yes sustainable wildlife economy. The common name, Blesbok, originates from ‘Bles’, the Afrikaans word for a ‘blaze’, which Distribution symbolises the white facial marking running down Historically, the Blesbok ranged across the Highveld from the animal’s horns to its nose, broken only grasslands of the Free State and Gauteng provinces, by the brown band above the eyes (Skinner & extending into northwestern KwaZulu-Natal, and through Chimimba 2005). -
Fitzhenry Yields 2016.Pdf
Stellenbosch University https://scholar.sun.ac.za ii DECLARATION By submitting this dissertation 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. Date: March 2016 Copyright © 2016 Stellenbosch University All rights reserved Stellenbosch University https://scholar.sun.ac.za iii GENERAL ABSTRACT Fallow deer (Dama dama), although not native to South Africa, are abundant in the country and could contribute to domestic food security and economic stability. Nonetheless, this wild ungulate remains overlooked as a protein source and no information exists on their production potential and meat quality in South Africa. The aim of this study was thus to determine the carcass characteristics, meat- and offal-yields, and the physical- and chemical-meat quality attributes of wild fallow deer harvested in South Africa. Gender was considered as a main effect when determining carcass characteristics and yields, while both gender and muscle were considered as main effects in the determination of physical and chemical meat quality attributes. Live weights, warm carcass weights and cold carcass weights were higher (p < 0.05) in male fallow deer (47.4 kg, 29.6 kg, 29.2 kg, respectively) compared with females (41.9 kg, 25.2 kg, 24.7 kg, respectively), as well as in pregnant females (47.5 kg, 28.7 kg, 28.2 kg, respectively) compared with non- pregnant females (32.5 kg, 19.7 kg, 19.3 kg, respectively). -
Beatragus Hunteri) in Arawale National Reserve, Northeastern, Kenya
The population size, abundance and distribution of the Critically Endangered Hirola Antelope (Beatragus hunteri) in Arawale National Reserve, Northeastern, Kenya. Francis Kamau Muthoni Terra Nuova, Transboundary Environmental Project, P.O. Box 74916, Nairobi, Kenya Email: [email protected] 1.0. Abstract. This paper outlines the spatial distribution, population size, habitat preferences and factors causing the decline of Hirola antelope in Arawale National Reserve (ANR) in Garissa and Ijara districts, north eastern Kenya. The reserve covers an area of 540Km2. The objectives of the study were to gather baseline information on hirola distribution, population size habitat preferences and human activities impacting on its existence. A sampling method using line transect count was used to collect data used to estimate the distribution of biological populations (Norton-Griffiths, 1978). Community scouts collected data using Global Positioning Systems (GPS) and recorded on standard datasheets for 12 months. Transect walks were done from 6.00Am to 10.00Am every 5th day of the month. The data was entered into a geo-database and analysed using Arcmap, Ms Excel and Access. The results indicate that the population of hirola in Arawale National Reserve were 69 individuals comprising only 6% of the total population in the natural geographic range of hirola estimated to be 1,167 individuals. It also revealed that hirola prefer open bushes and grasslands. The decline of the Hirola on its natural range is due to a combination of factors, including, habitat loss and degradation, competition with livestock, poaching and drought. Key words: Hirola Antelope Beatragus hunteri, GIS, Endangered Species 2.0. Introduction. The Hirola antelope (Beatragus hunteri) is a “Critically Endangered” species endemic to a small area in Southeast Kenya and Southwest Somalia. -
Western Zambian Sable: Are They a Geographic Extension of the Giant Sable Antelope?
View metadata, citation and similarWestern papers at core.ac.uk Zambian sable: Are they a brought to you by CORE geographic extension of theprovided by Stellenbosch University SUNScholar Repository giant sable antelope? Bettine Jansen van Vuuren1,2*, Terence J. Robinson1, Pedro VazPinto3, Richard Estes4 & Conrad A. Matthee1 1Evolutionary Genomics Group, Department Botany and Zoology, Stellenbosch University, Private Bag X1, Matieland, 7602 South Africa 2Centre for Invasion Biology, Department Botany and Zoology, Stellenbosch University, Private Bag X1, Matieland, 7602 South Africa 3Universidade Catolica de Angola, Rua Nossa Senhora da Muxima, 29 Luanda, Angola 45 Granite Street, Peterborough, NH 03458, U.S.A. Received 5 September 2008. Accepted 21 January 2010 The giant sable (Hippotragus niger variani ) is one of Africa’s most spectacular large antelope. Years of civil unrest in Angola, a highly localized distribution and interbreeding with its congener the roan antelope (H. equinus) has led to this subspecies being considered as critically endangered. Sable antelope occurring ~600 km to the east in western Zambia superficially resemble giant sable in phenotype, prompting speculation in the popular media that the distribution of giant sable may be larger than currently documented. Our aim here was to investigate the evolutionary placement of western Zambian sable using mitochon- drial DNA control region data. Phylogenetic analyses (maximum likelihood and Bayesian analyses) supported the monophyly of H. n. variani (Bayesian posterior probability of >0.95, bootstrap support >80%) and nested the western Zambian sable within H. n. niger. This find- ing was supported by an analysis of molecular variance that discretely grouped western F Zambian sable from giant sable ( ST = 0.645, P = 0.001). -
Hippotragus Equinus – Roan Antelope
Hippotragus equinus – Roan Antelope authorities as there may be no significant genetic differences between the two. Many of the Roan Antelope in South Africa are H. e. cottoni or equinus x cottoni (especially on private properties). Assessment Rationale This charismatic antelope exists at low density within the assessment region, occurring in savannah woodlands and grasslands. Currently (2013–2014), there are an observed 333 individuals (210–233 mature) existing on nine formally protected areas within the natural distribution range. Adding privately protected subpopulations and an Cliff & Suretha Dorse estimated 0.8–5% of individuals on wildlife ranches that may be considered wild and free-roaming, yields a total mature population of 218–294 individuals. Most private Regional Red List status (2016) Endangered subpopulations are intensively bred and/or kept in camps C2a(i)+D*†‡ to exclude predators and to facilitate healthcare. Field National Red List status (2004) Vulnerable D1 surveys are required to identify potentially eligible subpopulations that can be included in this assessment. Reasons for change Non-genuine: While there was an historical crash in Kruger National Park New information (KNP) of 90% between 1986 and 1993, the subpopulation Global Red List status (2008) Least Concern has since stabilised at c. 50 individuals. Overall, over the past three generations (1990–2015), based on available TOPS listing (NEMBA) Vulnerable data for nine formally protected areas, there has been a CITES listing None net population reduction of c. 23%, which indicates an ongoing decline but not as severe as the historical Endemic Edge of Range reduction. Further long-term data are needed to more *Watch-list Data †Watch-list Threat ‡Conservation Dependent accurately estimate the national population trend. -
Ecology of Red Deer a Research Review Relevant to Their Management in Scotland
Ecologyof RedDeer A researchreview relevant to theirmanagement in Scotland Instituteof TerrestrialEcology Natural EnvironmentResearch Council á á á á á Natural Environment Research Council Institute of Terrestrial Ecology Ecology of Red Deer A research review relevant to their management in Scotland Brian Mitchell, Brian W. Staines and David Welch Institute of Terrestrial Ecology Banchory iv Printed in England by Graphic Art (Cambridge) Ltd. ©Copyright 1977 Published in 1977 by Institute of Terrestrial Ecology 68 Hills Road Cambridge CB2 11LA ISBN 0 904282 090 Authors' address: Institute of Terrestrial Ecology Hill of Brathens Glassel, Banchory Kincardineshire AB3 4BY Telephone 033 02 3434. The Institute of Terrestrial Ecology (ITE) was established in 1973, from the former Nature Conservancy's research stations and staff, joined later by the Institute of Tree Biology and the Culture Centre of Algae and Protozoa. ITE contributes to and draws upon the collective knowledge of the fourteen sister institutes which make up the Natural Environment Research Council, spanning all the environmental sciences. The Institute studies the factors determining the structure, composition and processes of land and freshwater systems, and of individual plant and animal species. It is developing a Sounder scientific basis for predicting and modelling environmental trends arising from natural or man-made change. The results of this research are available to those responsible for the protection, management and wise use of our natural resources. Nearly half of ITE'Swork is research commissioned by customers, such as the Nature Conservancy Council who require information for wildlife conservation, the Forestry Commission and the Department of the Environment. The remainder is fundamental research supported by NERC. -
Connochaetes Gnou – Black Wildebeest
Connochaetes gnou – Black Wildebeest Blue Wildebeest (C. taurinus) (Grobler et al. 2005 and ongoing work at the University of the Free State and the National Zoological Gardens), which is most likely due to the historic bottlenecks experienced by C. gnou in the late 1800s. The evolution of a distinct southern endemic Black Wildebeest in the Pleistocene was associated with, and possibly driven by, a shift towards a more specialised kind of territorial breeding behaviour, which can only function in open habitat. Thus, the evolution of the Black Wildebeest was directly associated with the emergence of Highveld-type open grasslands in the central interior of South Africa (Ackermann et al. 2010). Andre Botha Assessment Rationale Regional Red List status (2016) Least Concern*† This is an endemic species occurring in open grasslands in the central interior of the assessment region. There are National Red List status (2004) Least Concern at least an estimated 16,260 individuals (counts Reasons for change No change conducted between 2012 and 2015) on protected areas across the Free State, Gauteng, North West, Northern Global Red List status (2008) Least Concern Cape, Eastern Cape, Mpumalanga and KwaZulu-Natal TOPS listing (NEMBA) (2007) Protected (KZN) provinces (mostly within the natural distribution range). This yields a total mature population size of 9,765– CITES listing None 11,382 (using a 60–70% mature population structure). This Endemic Yes is an underestimate as there are many more subpopulations on wildlife ranches for which comprehensive data are *Watch-list Threat †Conservation Dependent unavailable. Most subpopulations in protected areas are stable or increasing. -
EAZA Antelope & Giraffe
EAZA Antelope & Giraffe TAG Introduction & report on some activities Joint TAG chairs meeting 2016, Omaha Dr. Jens-Ove Heckel Zoo Landau in der Pfalz, Germany EAZA Antelope & Giraffe TAG chair [email protected] EAZA Antelope & Giraffe TAG • Antelope & Giraffe TAG continues as one of the largest and most complex TAGs representing 50 species (and approximately 90 taxa) in EAZA zoos • our remit: try to retain as many species as possible in healthy populations in EAZA collections • currently the TAG holds 11 EEPs and 11 ESBs; 4 species are part of ISBs; the remaining species are monitored (Mon-P, Mon-TAG). Chair Jens-Ove Heckel Landau Vice chair Sander Hofman Antwerp Vice chair (till 11.2015) Tania Gilbert Marwell Vice chair (since 12.2015) Kim Skalborg Simonsen Givskud Sub-group Okapi & Giraffe SG Sander Hofman Antwerp Sub-group Woodland antelope SG Kim Skalborg Simonsen Givskud Sub-group Savannah antelope SG Catrin Hammer Goerlitz Sub-group Aridlands antelope SG Ian Goodwin Marwell (Sub-group) (Mini antelope SG) (Klaus Müller-Schilling) (Hanover) Studbook keepers/Program managers EAZA Antelope & Giraffe TAG meeting 2015, Wroclaw Coordinator Conservation Tania Gilbert Marwell Coordinator Research Eulalia Moreno Almeria Advisor Veterinary Sven Hammer Goerlitz Advisor Genetics Rob Ogden Edinburgh Advisor Population management Laurie Bingaman Lackey USA Advisor Nutrition Marcus Clauss Zuerich Advisor Husbandry n.n. Advisor Education n.n. Regular support and advice also provided by: Exec. Coordinator - Collect. Coordin. & Conserv. Merel Zimmermann EPMAG / Population Management Kristin Leus Population Biologist - Collect. Coordin. & Conserv. Kristine Schad Good links to: IUCN SSC Antelope SG, IUCN Giraffe & Okapi SG/Giraffe Conservation Fdn., other EAZA Ungulate TAGs, BIAZA Hoof stock focus group, AZA Antelope & Giraffe TAG, Sahara Conservation Fund/SSIG etc. -
Animals of Africa
Silver 49 Bronze 26 Gold 59 Copper 17 Animals of Africa _______________________________________________Diamond 80 PYGMY ANTELOPES Klipspringer Common oribi Haggard oribi Gold 59 Bronze 26 Silver 49 Copper 17 Bronze 26 Silver 49 Gold 61 Copper 17 Diamond 80 Diamond 80 Steenbok 1 234 5 _______________________________________________ _______________________________________________ Cape grysbok BIG CATS LECHWE, KOB, PUKU Sharpe grysbok African lion 1 2 2 2 Common lechwe Livingstone suni African leopard***** Kafue Flats lechwe East African suni African cheetah***** _______________________________________________ Red lechwe Royal antelope SMALL CATS & AFRICAN CIVET Black lechwe Bates pygmy antelope Serval Nile lechwe 1 1 2 2 4 _______________________________________________ Caracal 2 White-eared kob DIK-DIKS African wild cat Uganda kob Salt dik-dik African golden cat CentralAfrican kob Harar dik-dik 1 2 2 African civet _______________________________________________ Western kob (Buffon) Guenther dik-dik HYENAS Puku Kirk dik-dik Spotted hyena 1 1 1 _______________________________________________ Damara dik-dik REEDBUCKS & RHEBOK Brown hyena Phillips dik-dik Common reedbuck _______________________________________________ _______________________________________________African striped hyena Eastern bohor reedbuck BUSH DUIKERS THICK-SKINNED GAME Abyssinian bohor reedbuck Southern bush duiker _______________________________________________African elephant 1 1 1 Sudan bohor reedbuck Angolan bush duiker (closed) 1 122 2 Black rhinoceros** *** Nigerian -
Common Eland
Tragelaphus oryx – Common Eland recognised, though their validity has been in dispute (Thouless 2013): Tragelaphus o. livingstonii (Sclater 1864; Livingstone's Eland): also called kaufmanni, niediecki, selousi and triangularis. It is found in the Central Zambezian Miombo woodlands i.e. south- central Africa (Angola, Zambia, Democratic Republic of the Congo, Zimbabwe, Mozambique and Malawi). Livingstone's Eland has a brown pelt with up to twelve stripes. Tragelaphus o. oryx (Pallas 1766; Cape Eland): also called alces, barbatus, canna and oreas. This subspecies is found south of the Zambezi river (South Africa, Botswana and Namibia). The fur is tawny, and adults lose their stripes. Regional Red List status (2016) Least Concern Tragelaphus o. pattersonianus (Lydekker 1906; East National Red List status (2004) Least Concern African Eland or Patterson's Eland): also called Reasons for change No change billingae. It is found in east Africa extending into the Somali arid areas, hence its common name. Its coat Global Red List status (2008) Least concern can have up to 12 stripes. TOPS listing (NEMBA) None Tragelaphus o. oryx occurs throughout the larger part of South Africa, but the far northern Limpopo Province CITES listing None bordering Zimbabwe is regarded as a transitional zone Endemic No between T. o. oryx and T. o. livingstonii or an area where they overlap. This argues the case that they should rather During drought conditions Eland roam extensively be described as ecotypes (in ecotypes, it is common for in order to meet forage and water requirements; in continuous, gradual geographic variation to impose the southern Kalahari during abnormally dry analogous phenotypic and/or genetic variation; this conditions, Eland were found to cover more than situation is called cline.). -
Copy of Roan Antelope Project
Roan Antelope Project Roan Antelope (Hippotragus equines) are Africa’s second largest antelope after the eland. Historically they were widely distributed in small herds over a large part of Swaziland. They became locally extinct when Swaziland’s very last freeranging roan antelope was poached at Maphiveni in 1961. Roan have become extremely rare across their entire natural range. The reason for their demise is probably a combination of factors which include poaching, diminishing range, stressinduced disease, predation, and competition by high density species. A small group of 4 roan (3 females, 1 bull) reintroduced to Mkhaya from Namibia perished because, we now believe, the animals were naïve to tickborne diseases in a densely tick hostile environment where mortalities overwhelmed recruitment. It is likely that the tickborne Theileria hippotragi disease played a large role. Theileria is a protozoal disease which is fatal to roan and sable antelope. The expertise of Dr Johan Steyl under the supervision of Prof. Leon Prozesky of the Onderstepoort Veterinary Faculty of the University of Pretoria has helped enormously with this project. The vector is the redlegged tick Rhipicephalus evertsi, which is abundant in Swaziland, but little was known about its impact on wildlife at the time of the Namibian introduction. Our Roan Antelope project got underway in 2002 after Dr Hamish Currie, founder and chief executive of Back to Africa, very generously committed to assist in restoring a viable population of roan antelope to Swaziland. Dr Hamish Currie wisely harnessed the expertise of Dr Johan Steyl whose guidance has without doubt been pivotal to the success of the project so far. -
Transboundary Species Project
TRANSBOUNDARY SPECIES PROJECT ROAN, SABLE AND TSESSEBE Rowan B. Martin Species Report for Roan, Sable and Tsessebe in support of The Transboundary Mammal Project of the Ministry of Environment and Tourism, Namibia facilitated by The Namibia Nature Foundation and World Wildlife Fund Living in a Finite Environment (LIFE) Programme Cover picture adapted from the illustrations by Clare Abbott in The Mammals of the Southern African Subregion by Reay H.N. Smithers Published by the University of Pretoria Republic of South Africa 1983 Transboundary Species Project – Background Study Roan, Sable and Tsessebe CONTENTS 1. BIOLOGICAL INFORMATION ...................................... 1 a. Taxonomy ..................................................... 1 b. Physical description .............................................. 3 c. Habitat ....................................................... 6 d. Reproduction and Population Dynamics ............................. 12 e. Distribution ................................................... 14 f. Numbers ..................................................... 24 g. Behaviour .................................................... 38 h. Limiting Factors ............................................... 40 2. SIGNIFICANCE OF THE THREE SPECIES ........................... 43 a. Conservation Significance ........................................ 43 b. Economic Significance ........................................... 44 3. STAKEHOLDING ................................................. 48 a. Stakeholders .................................................