Zsl Conservation Review 2013 3 Zsl Conservation Review / Where We Work
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Wild Or Bactrian Camel French: German: Wildkamel Spanish: Russian: Dikiy Verblud Chinese
1 of 4 Proposal I / 7 PROPOSAL FOR INCLUSION OF SPECIES ON THE APPENDICES OF THE CONVENTION ON THE CONSERVATION OF MIGRATORY SPECIES OF WILD ANIMALS A. PROPOSAL: Inclusion of the Wild camel Camelus bactrianus in Appendix I of the Convention on the Conservation of Migratory Species of Wild Animals: B. PROPONENT: Mongolia C. SUPPORTING STATEMENT 1. Taxon 1.1. Classis: Mammalia 1.2. Ordo: Tylopoda 1.3. Familia: Camelidae 1.4. Genus: Camelus 1.5. Species: Camelus bactrianus Linnaeus, 1758 1.6. Common names: English: Wild or Bactrian camel French: German: Wildkamel Spanish: Russian: Dikiy verblud Chinese: 2. Biological data 2.1. Distribution Wild populations are restricted to 3 small, remnant populations in China and Mongolia:in the Taklamakan Desert, the deserts around Lop Nur, and the area in and around region A of Mongolia’s Great Gobi Strict Protected Area (Reading et al 2000). In addition, there is a small semi-captive herd of wild camels being maintained and bred outside of the Park. 2.2. Population Surveys over the past several decades have suggested a marked decline in wild bactrian camel numbers and reproductive success rates (Zhirnov and Ilyinsky 1986, Anonymous 1988, Tolgat and Schaller 1992, Tolgat 1995). Researchers suggest that fewer than 500 camels remain in Mongolia and that their population appears to be declining (Xiaoming and Schaller 1996). Globally, scientists have recently suggested that less than 900 individuals survive in small portions of Mongolia and China (Tolgat and Schaller 1992, Hare 1997, Tolgat 1995, Xiaoming and Schaller 1996). However, most of the population estimates from both China and Mongolia were made using methods which preclude rigorous population estimation. -
Camelids: New Players in the International Animal Production Context
Tropical Animal Health and Production (2020) 52:903–913 https://doi.org/10.1007/s11250-019-02197-2 REVIEWS Camelids: new players in the international animal production context Mousa Zarrin1 & José L. Riveros2 & Amir Ahmadpour1,3 & André M. de Almeida4 & Gaukhar Konuspayeva5 & Einar Vargas- Bello-Pérez6 & Bernard Faye7 & Lorenzo E. Hernández-Castellano8 Received: 30 October 2019 /Accepted: 22 December 2019 /Published online: 2 January 2020 # Springer Nature B.V. 2020 Abstract The Camelidae family comprises the Bactrian camel (Camelus bactrianus), the dromedary camel (Camelus dromedarius), and four species of South American camelids: llama (Lama glama),alpaca(Lama pacos)guanaco(Lama guanicoe), and vicuña (Vicugna vicugna). The main characteristic of these species is their ability to cope with either hard climatic conditions like those found in arid regions (Bactrian and dromedary camels) or high-altitude landscapes like those found in South America (South American camelids). Because of such interesting physiological and adaptive traits, the interest for these animals as livestock species has increased considerably over the last years. In general, the main animal products obtained from these animals are meat, milk, and hair fiber, although they are also used for races and work among other activities. In the near future, climate change will likely decrease agricultural areas for animal production worldwide, particularly in the tropics and subtropics where competition with crops for human consumption is a major problem already. In such conditions, extensive animal production could be limited in some extent to semi-arid rangelands, subjected to periodical draughts and erratic patterns of rainfall, severely affecting conventional livestock production, namely cattle and sheep. -
Bactrian Camel, Two-Humped Camel
Camelus ferus/bactrianus Common name: Bactrian camel, two-humped camel Local name: Havtagai (Mongolian), Wildkamel (German), Jya nishpa yapung (Ladakhi) Classification: Kingdom: Animalia Phylum: Chordata Class: Mammalia Order: Artiodactyla Family: Camelidae Genus: Camelus Species: ferus/bactrianus Profile: The scientific name of the wild Bactrian camel is Camelus ferus, while the domesticated form is called Camelus bactrianus. The distinctive feature of the animal is that it is two-humped whereas the Dromedary camel has a single hump. DNA tests have revealed that there are two or three distinct genetic differences and about 3% base difference between the wild and domestic populations of Bactrian camels. They also differ physically. The wild Bactrian camel is smaller and slender than the domestic breed. The wild camels have a sandy gray- brown coat while the domestic ones have a dark brown coat. The predominant difference between them however is the shape of the humps. While that of the wild camel are small and pyramid-like, those of the domestic ones are large and irregular. The face of a Bactrian camel is long and triangular with a split upper lip. The Bactrian camel is highly adapted to surviving the cold desert climate. Each foot has an undivided sole with two large toes that can spread wide apart for walking on sand. The ears and nose are lined with hair to protect against sand and the muscular nostrils can be closed during sandstorms. The eyes are protected from sand and debris by a double layer of long eyelashes while bushy eyebrows give protection from the sun. It grows a thick shaggy coat during winter, which is shed very rapidly in spring to give the animal a shorn look. -
In Search of the Extinct Hutia in Cave Deposits of Isla De Mona, P.R. by Ángel M
In Search of the Extinct Hutia in Cave Deposits of Isla de Mona, P.R. by Ángel M. Nieves-Rivera, M.S. and Donald A. McFarlane, Ph.D. Isolobodon portoricensis, the extinct have been domesticated, and its abundant (14C) date was obtained on charcoal and Puerto Rican hutia (a large guinea-pig like remains in kitchen middens indicate that it bone fragments from Cueva Negra, rodent), was about the size of the surviving formed part of the diet for the early settlers associated with hutia bones (Frank, 1998). Hispaniolan hutia Plagiodontia (Rodentia: (Nowak, 1991; Flemming and MacPhee, This analysis yielded an uncorrected 14C age Capromydae). Isolobodon portoricensis was 1999). This species of hutia was extinct, of 380 ±60 before present, and a corrected originally reported from Cueva Ceiba (next apparently shortly after the coming of calendar age of 1525 AD, (1 sigma range to Utuado, P.R.) in 1916 by J. A. Allen (1916), European explorers, according to most 1480-1655 AD). This date coincides with the and it is known today only by skeletal remains historians. final occupation of Isla de Mona by the Taino from Hispaniola (Dominican Republic, Haiti, The first person to take an interest in the Indians (1578 AD; Wadsworth 1977). The Île de la Gonâve, ÎIe de la Tortue), Puerto faunal remains of the caves of Isla de Mona purpose of this article is to report some new Rico (mainland, Isla de Mona, Caja de was mammalogist Harold E. Anthony, who paleontological discoveries of the Puerto Muertos, Vieques), the Virgin Islands (St. in 1926 collected the first Puerto Rican hutia Rican hutia in cave deposits of Isla de Mona Croix, St. -
ANIMAL WELFARE POLICY TOOLKIT CREATED by INTREPID TRAVEL & WORLD ANIMAL PROTECTION Tourism Will Return
ANIMAL WELFARE POLICY TOOLKIT CREATED BY INTREPID TRAVEL & WORLD ANIMAL PROTECTION Tourism Will Return. Cruelty Should Not. Nearly 550,000 wild animals are currently enduring lifetimes of suffering at tourist entertainment venues globally. Activities such as riding elephants, taking photos with tigers, lion walks and dolphin performances are examples of popular tourist attractions that can cause lifelong trauma for wild animals. The COVID-19 crisis has provided us with an opportunity to redefine what tourism looks like once travel resumes and to use this time to forge a new path for a more responsible, sustainable and ethical future. As travel providers who facilitate experiences all around the world, it is our responsibility to protect the environment and all of its living species. The very least we can do is ensure our practices are not causing harm to the wildlife who call the destinations we visit home. This toolkit has been created by Intrepid Travel, a certified B Corporation and the first global tour operator to ban elephant rides, and World Animal Protection, a global animal welfare organisation - leading on responsible wildlife tourism. It is our hope that the Animal Welfare Policy Toolkit will help the tourism industry rebuild more ethically during the COVID-caused travel shutdowns. This resource includes tips on how to draft and implement more animal-friendly practices within a tourism organisation, as well as an editable policy template for businesses to get started on their journey. While this toolkit has been endorsed by both parties to encourage tourism businesses to adopt more ethical practices concerning animals, in particular wildlife, this template is meant to be used as a guideline. -
Ecologia De Les Illes
Observations on the habitat and ecology of the Hispaniolan Solenodon (Solenodon paradoxus) in the Dominican Republic Jose A. OTTENWALDER Proyecto Biodiversidad GEF-PNUD/ONAPLAN. Programa de las Naciones para el Desarrollo (PNUD) y Oficina Nacional de Planificacion. Apartado 1424, Mirador Sur. Santo Domingo, Republica Dominicana Ottenwalder, J.A. 1999. Observations on the habitat and ecology of the Hispaniolan Solenodon (Solenodon paradoxus) in the Dominican Republic. Mon. Soc. Hist. Nat. Balears, 6 I Mon. Inst. Est. Bal. 66: 123-168. ISBN: 84- 87026-86-9. Palma de Mallorca. The habitat of the Hispaniolan Solenodon (Solenodon paradoxus) was investiga ted in the Dominican Republic in relation to particular environmental parameters (geomorphology, geologicalstructure, soil type, elevation, life zone, vegetation, rainfall, and temperature). Results are discussed in relation to relevant species environment interactions, particularly habitat preferences and life history patterns of the species. Comparisons on the habitat, ecology and life history are made bet ween S. paradoxus and the Cuban Solenodon (S. cubanus), the only other living member of the genus. Keywords: Solenodon, Caribbean, Antilles, Ecology, Conservation Biology. Observaciones sobre el habitat y ecologia del Solenodon de la Hispaniola (Solenodon paradox us) en la Republica Dominicana. EI habitat del Solenodon de la Hispaniola (Solenodon paradoxus) fue estudiado en la Republica Dominicana en relacion a una serie de parametres ambientales (geomorfologia, estructura geologica, tipo de suelo, elevacion, zona de vida, for macion vegetal, precipitacion, y temperatura). Las relaciones especie-habitat son analizadas usando un modelo empirico descriptivo. Las observaciones sobre inte racciones especie-rnedio ambiente resultantes son discutidas particularmente en relacion a preferencias aparentes de habitat y a los patrones de historia natural de la especie. -
Investigating Evolutionary Processes Using Ancient and Historical DNA of Rodent Species
Investigating evolutionary processes using ancient and historical DNA of rodent species Thesis submitted for the degree of Doctor of Philosophy (PhD) University of London Royal Holloway University of London Egham, Surrey TW20 OEX Selina Brace November 2010 1 Declaration I, Selina Brace, declare that this thesis and the work presented in it is entirely my own. Where I have consulted the work of others, it is always clearly stated. Selina Brace Ian Barnes 2 “Why should we look to the past? ……Because there is nowhere else to look.” James Burke 3 Abstract The Late Quaternary has been a period of significant change for terrestrial mammals, including episodes of extinction, population sub-division and colonisation. Studying this period provides a means to improve understanding of evolutionary mechanisms, and to determine processes that have led to current distributions. For large mammals, recent work has demonstrated the utility of ancient DNA in understanding demographic change and phylogenetic relationships, largely through well-preserved specimens from permafrost and deep cave deposits. In contrast, much less ancient DNA work has been conducted on small mammals. This project focuses on the development of ancient mitochondrial DNA datasets to explore the utility of rodent ancient DNA analysis. Two studies in Europe investigate population change over millennial timescales. Arctic collared lemming (Dicrostonyx torquatus) specimens are chronologically sampled from a single cave locality, Trou Al’Wesse (Belgian Ardennes). Two end Pleistocene population extinction-recolonisation events are identified and correspond temporally with - localised disappearance of the woolly mammoth (Mammuthus primigenius). A second study examines postglacial histories of European water voles (Arvicola), revealing two temporally distinct colonisation events in the UK. -
Solenodon Genome Reveals Convergent Evolution of Venom in Eulipotyphlan Mammals
Solenodon genome reveals convergent evolution of venom in eulipotyphlan mammals Nicholas R. Casewella,1, Daniel Petrasb,c, Daren C. Cardd,e,f, Vivek Suranseg, Alexis M. Mychajliwh,i,j, David Richardsk,l, Ivan Koludarovm, Laura-Oana Albulescua, Julien Slagboomn, Benjamin-Florian Hempelb, Neville M. Ngumk, Rosalind J. Kennerleyo, Jorge L. Broccap, Gareth Whiteleya, Robert A. Harrisona, Fiona M. S. Boltona, Jordan Debonoq, Freek J. Vonkr, Jessica Alföldis, Jeremy Johnsons, Elinor K. Karlssons,t, Kerstin Lindblad-Tohs,u, Ian R. Mellork, Roderich D. Süssmuthb, Bryan G. Fryq, Sanjaya Kuruppuv,w, Wayne C. Hodgsonv, Jeroen Kooln, Todd A. Castoed, Ian Barnesx, Kartik Sunagarg, Eivind A. B. Undheimy,z,aa, and Samuel T. Turveybb aCentre for Snakebite Research & Interventions, Liverpool School of Tropical Medicine, Pembroke Place, L3 5QA Liverpool, United Kingdom; bInstitut für Chemie, Technische Universität Berlin, 10623 Berlin, Germany; cCollaborative Mass Spectrometry Innovation Center, University of California, San Diego, La Jolla, CA 92093; dDepartment of Biology, University of Texas at Arlington, Arlington, TX 76010; eDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; fMuseum of Comparative Zoology, Harvard University, Cambridge, MA 02138; gEvolutionary Venomics Lab, Centre for Ecological Sciences, Indian Institute of Science, 560012 Bangalore, India; hDepartment of Biology, Stanford University, Stanford, CA 94305; iDepartment of Rancho La Brea, Natural History Museum of Los Angeles County, Los Angeles, -
Review of Zoos' Conservation and Education Contribution
Review of Zoos’ Conservation and Education Contribution Contract No : CR 0407 Prepared for: Jane Withey and Margaret Finn Defra Biodiversity Programme Zoos Policy Temple Quay House Bristol BS1 6EB Prepared by: ADAS UK Ltd Policy Delivery Group Woodthorne Wergs Road Wolverhampton WV6 8TQ Date: April 2010 Issue status: Final Report 0936648 ADAS Review of Zoos’ Conservation and Education Contribution Acknowledgements The authors would like to thank in particular the zoos, aquariums and animal parks that took part in the fieldwork and case studies. We are also grateful to members of the Consultation Group and the Steering Group for their advice and support with this project. The support of Tom Adams, Animal Health, is also acknowledged for assistance with sample design. Project Team The ADAS team that worked on this study included: • Beechener, Sam • Llewellin, John • Lloyd, Sian • Morgan, Mair • Rees, Elwyn • Wheeler, Karen The team was supported by the following specialist advisers: • BIAZA (British and Irish Association of Zoos and Aquariums); and • England Marketing - provision of telephone fieldwork services I declare that this report represents a true and accurate record of the results obtained/work carried out. 30 th April 2010 Sam Beechener and Mair Morgan (Authors’ signature) (Date) 30 th April 2010 John Llewellin (Verifier’s signature) (Date) Executive Summary Executive Summary Objectives The aims of this project were to collect and assess information about the amount and type of conservation and education work undertaken by zoos in England. On the basis of that assessment, and in the light of the Secretary of State’s Standards of Modern Zoo Practice (SSSMZP) and the Zoos Forum Handbook (2008 - including the Annexes to Chapter 2), the project will make recommendations for: • minimum standards for conservation and education in a variety of sizes of zoo; and • methods for zoo inspectors to enable them to assess zoo conservation and educational activities. -
The Last Survivors: Current Status and Conservation of the Non-Volant Land
1 The Last Survivors: current status and conservation of the non-volant land 2 mammals of the insular Caribbean 3 4 SAMUEL T. TURVEY,* ROSALIND J. KENNERLEY, JOSE M. NUÑEZ-MIÑO, AND RICHARD P. 5 YOUNG 6 7 Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY (STT) 8 Durrell Wildlife Conservation Trust, Les Augrès Manor, Trinity, Jersey JE3 5BP, Channel 9 Islands (RJK, JNM, RPY) 10 11 *Correspondent: [email protected] 12 13 Running header: Status of Caribbean land mammals 14 1 15 The insular Caribbean is among the few oceanic-type island systems colonized by non-volant 16 land mammals. This region also has experienced the world’s highest levels of historical 17 mammal extinctions, with at least 29 species lost since AD 1500. Representatives of only 2 18 land-mammal families (Capromyidae and Solenodontidae) now survive, in Cuba, Hispaniola, 19 Jamaica, and the Bahama Archipelago. The conservation status of Caribbean land mammals 20 is surprisingly poorly understood. The most recent IUCN Red List assessment, from 2008, 21 recognized 15 endemic species, of which 13 were assessed as threatened. We reassessed all 22 available baseline data on the current status of the Caribbean land-mammal fauna within the 23 framework of the IUCN Red List, to determine specific conservation requirements for 24 Caribbean land-mammal species using an evidence-based approach. We recognize only 13 25 surviving species, 1 of which is not formally described and cannot be assessed using IUCN 26 criteria; 3 further species previously considered valid are interpreted as junior synonyms or 27 subspecies. -
The Behavior of Solenodon Paradoxus in Captivity with Comments on the Behavior of Other Insectivora
The Behavior of Solenodon paradoxus in Captivity with Comments on the Behavior of Other Insectivora JOHN F. EISENBERG1 Department of Zoology, University of Maryland & EDWIN GOULD2 Department of Mental Hygiene, Laboratory of Comparative Behavior, Johns Hopkins University (Plates I & II) I. INTRODUCTION For comparative purposes the authors utilized Solenodon paradoxus, confined to the island the extensive collection of living tenrecs main- of Hispaniola, and S. cubanus, endemic to Cuba, tained by Dr. Gould at Johns Hopkins Uni- versity, and drew upon their previous behavioral comprise the sole living members of the family studies of insectivores, which have already been Solenodontidae. A full-grown specimen of S. published in part elsewhere (Eisenberg, 1964; paradoxus may weigh up to 1 kgm. and attain a Gould, 1964, 1965). head and body length of 300 mm. Although large size and primitive molar cusp pattern have led II. SPECIMENS AND MAINTENANCE taxonomists to include this genus with the tenrecs Four specimens of Solenodon paradoxus (one of Madagascar, further morphological studies male, three females) were purchased from a have led certain workers to conclude that Sol- dealer in the Dominican Republic. The male enodon is a primitive soricoid more closely allied (M) and one female (J) were immature and, to the shrews than to the zalambdadont tenrecs extrapolating from their weights (Mohr, 1936 (McDowell, 1958). II), were judged to be four and six months old, The behavior of S. paradoxus was reviewed respectively. The juveniles were studied as a by Dr. Erna Mohr (1936-38). Since her series of pair by Dr. Eisenberg. In addition, all four ani- papers, however, much more has been learned mals were employed in two-animal encounters concerning the behavior of not only the soleno- and were recorded during studies of vocal com- don but also the insectivores of the families munication. -
2005 – Building for the Future
2005 – 2006 2005 – Building for the future Working with communities is an important part of ZSL’s effort to involve local people in the welfare of their wildlife Reading this year’s Living Conservation report I am struck by the sheer breadth and vitality of ZSL’s conservation work around the world. It is also extremely gratifying to observe so many successes, ranging from our international animal conservation and scientific research programmes to our breeding of endangered animals and educational projects. Equally rewarding was our growing Zoology at the University of financial strength during 2005. In a year Cambridge. This successful overshadowed by the terrorist attacks collaboration with our Institute of in the capital, ZSL has been able to Zoology has generated numerous demonstrate solid and sustained programmes of research. We are financial growth, with revenue from our delighted that this partnership will website, retailing, catering and business continue for another five years. development operations all up on last Our research projects continued to year. influence policy in some of the world’s In this year’s report we have tried to leading conservation fields, including give greater insight into some of our the trade in bushmeat, the assessment most exciting conservation programmes of globally threatened species, disease – a difficult task given there are so risks to wildlife, and the ecology and many. Fortunately, you can learn more behaviour of our important native about our work on our award-winning* species. website www.zsl.org (*Best Website – At Regent’s Park we opened another Visit London Awards November 2005). two new-look enclosures.