Climate Change Impacts on Biodiversity

Total Page:16

File Type:pdf, Size:1020Kb

Climate Change Impacts on Biodiversity Climate Change Impacts on Biodiversity and Protected Areas in West Africa Summary of the main outputs of the PARCC project, Protected Areas Resilient to Climate Change in West Africa A GEF-funded project officially known as ‘Evolution of PA systems with regard to climate change in the West Africa region’ Climate Change Impacts on Biodiversity and Protected Areas in West Africa Summary of the main outputs of the PARCC project, Protected Areas Resilient to Climate Change in West Africa © 2016 United Nations Environment Programme ISBN: 978-92-807-3515-4 DEW/1935/CA The United Nations Environment Programme World Conservation Monitoring Centre (UNEP-WCMC) is the specialist biodiversity assessment centre of the United Nations Environment Programme (UNEP), the world’s foremost intergovernmental environmental organisation. The Centre has been in operation for over 30 years, combining scientific research with practical policy advice. Climate Change Impacts on Biodiversity and Protected Areas in West Africa has been compiled and edited by Elise Belle, on the basis of the main outputs of the project, with funding from the Global Environment Facility (GEF) via UNEP. Copyright: 2016. United Nations Environment Programme. Reproduction: This publication may be reproduced for educational or non-profit purposes without special permission, provided acknowledgement to the source is made. Reuse of any figures is subject to permission from the original rights holders. No use of this publication may be made for resale or any other commercial purpose without permission in writing from UNEP. Applications for permission, with a statement of purpose and extent of reproduction, should be sent to the Director, DCPI, UNEP, P.O. Box 30552, Nairobi, Kenya. Disclaimer: The contents of this report do not necessarily reflect the views or policies of UNEP, contributory organisations or editors. The designations employed and the presentations of material in this report do not imply the expression of any opinion whatsoever on the part of UNEP or contributory organisations, editors or publishers concerning the legal status of any country, territory, city area or its authorities, or concerning the delimitation of its frontiers or boundaries or the designation of its name, frontiers or boundaries. The mention of a commercial entity or product in this publication does not imply endorsement by UNEP. Citation: Belle E.M.S., Burgess N.D., Misrachi M., Arnell A., Masumbuko B., Somda J., Hartley A., Jones R., Janes T., McSweeney C., Mathison C., Buontempo C., Butchart S., Willis S.G., Baker D.J., Carr J., Hughes A., Foden W., Smith R.J., Smith J., Stolton S., Dudley N., Hockings M., Mulongoy J., and Kingston N. 2016. Climate Change Impacts on Biodiversity and Protected Areas in West Africa, Summary of the main outputs of the PARCC project, Protected Areas Resilient to Climate Change in West Africa. UNEP-WCMC, Cambridge, UK. Available From: UNEP-WCMC, 219 Huntingdon Road, Cambridge CB3 0DL, UK Tel: +44 1223 277314; Fax: +44 1223 277136 Email: [email protected] URL: http://www.unep-wcmc.org Cover pictures: Elephants in Nazinga game reserve, Burkina Faso (front); Kakum national park, Ghana (back). Copyright: Elise Belle UNEP World Conservation Monitoring Centre (UNEP-WCMC) 219 Huntingdon Road, Cambridge CB3 0DL, UK UNEP promotes Tel: +44 1223 277314 environmentally sound www.unep-wcmc.org practices globally and in its own activities. Our distribution policy aims to reduce UNEP’s carbon footprint. Contents Executive Summary ...............................................................v Introduction ..................................................................... 1 Project objectives and structure .....................................................2 A project in partnership............................................................2 Climate projections for the West Africa region .........................................3 Future species distribution in the face of climate change.................................11 Species vulnerability according to their biological traits .................................13 Integration of species distribution and vulnerability assessments......................... 17 Assessment of the connectivity of the West African PA network..........................20 Identification of priority areas for biodiversity conservation .............................23 Links between PAs, communities, and climate change..................................29 PA management, financing and monitoring within the framework of climate change ........ 31 Transboundary pilot site activities in order to enhance PA resilience . 33 Regional and national capacity building .............................................40 Adaptation strategies and policy recommendations ....................................44 Guidelines for PA managers in the face of climate change ...............................48 Integration of the project results into Protected Planet . 51 List of technical reports ...........................................................52 i Acknowledgements We would like to thank all the representatives of government agencies that took part in the PARCC project, either as Project Steering Committee members or National Liaison Officers, namely Mr Kotchikpa Okoumassou and Mr Pyoabalo Alaba for Togo; Mrs Haidara Souhayata, Mr Zan Moussa Samaké, Mr Alamir Sinna Touré, Mr Sékou Koné and Mr Issa Fahiri Koné for Mali; Mr Brahim Hissein Dagga, Mr Gaourang Mamadi N’Garkelo, and Mr Hakim Djibril for Chad; Mr Famara Drammeh, Mr Momodou Suwareh, Mr Momodou Sarr, and Mrs Ndey Bakurin for The Gambia; and Mrs Kate Garnett and Mr Kolleh Bangura for Sierra Leone. We are grateful to all the project partners, especially our main regional partner, the International Union for Conservation of Nature, Central and West Africa Programme (IUCN PACO), and all our technical collaborators, including the UK Met Office Hadley Centre, BirdLife International and Africa, Durham University, IUCN Global Species Programme, and the Durrell Institute of Conservation and Ecology (DICE) from the University of Kent, for their essential scientific contributions to the project. This project was funded by the Global Environment Facility (GEF) through UNEP. We would like to thank all the UNEP DEPI/GEF staff, including the Task Managers Esther Mwangi and Ersin Esen, Funds Management Officer Shakira Khawaja, as well as Anthony Kamau and George Saddimbah. We also thank Mohammed Sessay, Neville Ash and Mette Løyche Wilkie from UNEP DEPI, as well as Jon Hutton, Tim Johnson, Pamela Abbot, Sharon Hall, Judith Haste, Alex Gee, Safiye Bilgin-Foxall, Erin Dillon and John Blenkharn from UNEP-WCMC. We are also grateful to all the reviewers of the project outputs, including Famara Drammeh, Tommy Garnett, Gabriel Segniagbeto, Wilfran Moufouma Okia, Edward Perry, Stephen Woodley, Piero Visconti, Rebecca Mant, Cordula Epple, Fiona Danks, Robert Munroe, Jerry Harrison, as well as all members of UNEP-WCMC’s Protected Areas Programme, who supported the project in various ways, including Sylvia Wicander, Murielle Misrachi, Heather Bingham, Marine Deguignet, and Edward Lewis. Finally, we would like to thank Charles Besancon and Jonathan Smith who developed and set up the project, and all the participants to the national and regional workshops of the project. ii Roan antelope, Hippotragus equinus, in the National Park of Bouba Ndjidda, Cameroon. ©Bertrand Geismar Foreword Protected areas have long been used as a key strategy to conserve species and ecosystems. However, they are under increasing threat from climate change, which is now exacerbating other anthropogenic pressures. The Protected Areas Resilient to Climate Change (PARCC) project, funded by the GEF and implemented by UNEP, sought to address this issue by developing science-based tools to assess the vulnerability of protected areas, and by formulating strategies and recommendations to improve the management of protected areas in the face of climate change. The geographic area of the project was West Africa, with more detailed work implemented in The Gambia, Sierra Leone, Mali, Togo and Chad. This publication summarizes the main outputs of the PARCC project, from regional climate projections to pilot activities at transboundary protected areas, and includes among many other outputs, species vulnerability assessments, species distribution models, protected area connectivity analyses, regional and national conservation planning systems, as well as capacity development activities and policy recommendations. All the innovative science-based methodologies that were developed for the West Africa region can be applied in other regions. These tools include the integration of species distribution models with species vulnerability assessments based on biological traits to identify the protected areas most vulnerable to climate change, in addition to connectivity analysis of the existing protected area network that allowed the identification of the most important protected areas to maintain connectivity in the region. Furthermore, the systematic conservation planning systems that were developed lead to the identification of priority areas for conservation and the locations where new protected areas should be located, based not only on current biological data, but also taking into account the expected future distribution of species under climate change. Finally, the capacity development activities, carried out at multiple institutional levels through national and regional
Recommended publications
  • Systematics and Phylogeography of the Widely Distributed African Skink Trachylepis Varia Species Complex
    See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/321703844 Systematics and phylogeography of the widely distributed African skink Trachylepis varia species complex Article in Molecular Phylogenetics and Evolution · December 2017 DOI: 10.1016/j.ympev.2017.11.014 CITATIONS READS 14 709 2 authors: Jeffrey Weinell A. M. Bauer University of Kansas Villanova University 17 PUBLICATIONS 91 CITATIONS 680 PUBLICATIONS 12,217 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Reptile Database View project Journal of Animal Diversity (ISSN: 2676-685X; http://jad.lu.ac.ir) View project All content following this page was uploaded by Jeffrey Weinell on 15 December 2017. The user has requested enhancement of the downloaded file. Molecular Phylogenetics and Evolution 120 (2018) 103–117 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Systematics and phylogeography of the widely distributed African skink T Trachylepis varia species complex ⁎ Jeffrey L. Weinell , Aaron M. Bauer Department of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA 19085, USA ARTICLE INFO ABSTRACT Keywords: A systematic study of the Trachylepis varia complex was conducted using mitochondrial and nuclear DNA Africa markers for individuals sampled across the species range. The taxonomic history of T. varia has been complicated Lygosominae and its broad geographic distribution and considerable phenotypic variation has made taxonomic revision dif- Phylogenetics ficult, leading earlier taxonomists to suggest that T. varia is a species complex. We used maximum likelihood and Phylogeography Bayesian inference to estimate gene trees and a multilocus time-tree, respectively, and we used these trees to Trachylepis damarana identify the major clades (putative species) within T.
    [Show full text]
  • Arrival and Diversification of Mabuyine Skinks (Squamata: Scincidae) in the Neotropics Based on a Fossil-Calibrated Timetree
    Arrival and diversification of mabuyine skinks (Squamata: Scincidae) in the Neotropics based on a fossil-calibrated timetree Anieli Guirro Pereira and Carlos G. Schrago Department of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, RJ, Brazil ABSTRACT Background. The evolution of South American Mabuyinae skinks holds significant biogeographic interest because its sister lineage is distributed across the African continent and adjacent islands. Moreover, at least one insular species, Trachylepis atlantica, has independently reached the New World through transoceanic dispersal. To clarify the evolutionary history of both Neotropical lineages, this study aimed to infer an updated timescale using the largest species and gene sampling dataset ever assembled for this group. By extending the analysis to the Scincidae family, we could employ fossil information to estimate mabuyinae divergence times and carried out a formal statistical biogeography analysis. To unveil macroevolutionary patterns, we also inferred diversification rates for this lineage and evaluated whether the colonization of South American continent significantly altered the mode of Mabuyinae evolution. Methods. A time-calibrated phylogeny was inferred under the Bayesian framework employing fossil information. This timetree was used to (i) evaluate the historical biogeography of mabuiyines using the statistical approach implemented in Bio- GeoBEARS; (ii) estimate macroevolutionary diversification rates of the South American Mabuyinae lineages and the patterns of evolution of selected traits, namely, the mode of reproduction, body mass and snout–vent length; (iii) test the hypothesis of differential macroevolutionary patterns in South American lineages in BAMM and GeoSSE; and Submitted 21 November 2016 (iv) re-evaluate the ancestral state of the mode of reproduction of mabuyines.
    [Show full text]
  • Reproductionreview
    REPRODUCTIONREVIEW The evolution of viviparity: molecular and genomic data from squamate reptiles advance understanding of live birth in amniotes James U Van Dyke, Matthew C Brandley and Michael B Thompson School of Biological Sciences, University of Sydney, A08 Heydon-Laurence Building, Sydney, New South Wales 2006, Australia Correspondence should be addressed to J U Van Dyke; Email: [email protected] Abstract Squamate reptiles (lizards and snakes) are an ideal model system for testing hypotheses regarding the evolution of viviparity (live birth) in amniote vertebrates. Viviparity has evolved over 100 times in squamates, resulting in major changes in reproductive physiology. At a minimum, all viviparous squamates exhibit placentae formed by the appositions of maternal and embryonic tissues, which are homologous in origin with the tissues that form the placenta in therian mammals. These placentae facilitate adhesion of the conceptus to the uterus as well as exchange of oxygen, carbon dioxide, water, sodium, and calcium. However, most viviparous squamates continue to rely on yolk for nearly all of their organic nutrition. In contrast, some species, which rely on the placenta for at least a portion of organic nutrition, exhibit complex placental specializations associated with the transport of amino acids and fatty acids. Some viviparous squamates also exhibit reduced immunocompetence during pregnancy, which could be the result of immunosuppression to protect developing embryos. Recent molecular studies using both candidate-gene and next-generation sequencing approaches have suggested that at least some of the genes and gene families underlying these phenomena play similar roles in the uterus and placenta of viviparous mammals and squamates.
    [Show full text]
  • First Records of the Rainbow Mabuya Trachylepis Quinquetaeniata (Lichtenstein, 1823) (Squamata: Scincidae) in Algeria
    Herpetology Notes, volume 9: 167-169 (2016) (published online on 24 August 2016) First records of the Rainbow Mabuya Trachylepis quinquetaeniata (Lichtenstein, 1823) (Squamata: Scincidae) in Algeria Rouag Rachid1,*, Dahel Ramdane2, Rahmouni Salima2, Benkacimi Sara2 and Ziane Nadia3 The genus Mabuya represents a species-rich group of arboreal but several species (e.g. T. planifrons, T. mostly medium sized lizards of the family Scincidae, maculilabris) spend much of their time in trees (Spawls subfamily Lygosominae. It was one of the largest genera et al., 2002). of the family Scincidae, and the only skink genus with a The Five-lined Mabuya (T. quinquetaeniata), also circumtropical distribution (Greer and Broadley, 2000; called Rainbow Mabuya or blue-tailed Skink (due to the Greer and Nussbaum, 2000). Phylogenetic studies blue tail) Trachylepis quinquetaeniata is a medium sized published during the last decade led to the splitting of lizard reaching a total length of about 20 centimeters. The the genus Mabuya sensu lato into four geographically coloration of this species is quite variable, depending distinct monophyletic genera (Eutropis in Asia, Mabuya on the gender and the age. The scales are glossy, with sensu stricto in the Neotropics and Chioninia in the Cape metallic reflections. The basic colour is usually olive- Verde archipelago (Mausfeld et al., 2002; Carranza and brown or dark brown, sometimes with pearly whitish Arnold, 2003), with the African skinks placed in the spots and with three light olive or dark brown stripes genus Trachylepis (Mausfeld et al., 2002; Bauer et al., running from the head to the electric blue tail. These 2003).
    [Show full text]
  • Reptiles & Amphibians of Kirindy
    REPTILES & AMPHIBIANS OF KIRINDY KIRINDY FOREST is a dry deciduous forest covering about 12,000 ha and is managed by the Centre National de Formation, dʹEtudes et de Recherche en Environnement et Foresterie (CNFEREF). Dry deciduous forests are among the world’s most threatened ecosystems, and in Madagascar they have been reduced to 3 per cent of their original extent. Located in Central Menabe, Kirindy forms part of a conservation priority area and contains several locally endemic animal and plant species. Kirindy supports seven species of lemur and Madagascarʹs largest predator, the fossa. Kirindy’s plants are equally notable and include two species of baobab, as well as the Malagasy endemic hazomalany tree (Hazomalania voyroni). Ninety‐nine per cent of Madagascar’s known amphibians and 95% of Madagascar’s reptiles are endemic. Kirindy Forest has around 50 species of reptiles, including 7 species of chameleons and 11 species of snakes. This guide describes the common amphibians and reptiles that you are likely to see during your stay in Kirindy forest and gives some field notes to help towards their identification. The guide is specifically for use on TBA’s educational courses and not for commercial purposes. This guide would not have been possible without the photos and expertise of Marius Burger. Please note this guide is a work in progress. Further contributions of new photos, ids and descriptions to this guide are appreciated. This document was developed during Tropical Biology Association field courses in Kirindy. It was written by Rosie Trevelyan and designed by Brigid Barry, Bonnie Metherell and Monica Frisch.
    [Show full text]
  • Reproductive Specializations in a Viviparous African Skink: Implications for Evolution and Biological Conservation
    Trinity College Trinity College Digital Repository Faculty Scholarship 8-2010 Reproductive Specializations in a Viviparous African Skink: Implications for Evolution and Biological Conservation Daniel G. Blackburn Trinity College, [email protected] Alexander F. Flemming University of Stellenbosch Follow this and additional works at: https://digitalrepository.trincoll.edu/facpub Part of the Biology Commons Herpetological Conservation and Biology 5(2):263-270. Symposium: Reptile Reproduction REPRODUCTIVE SPECIALIZATIONS IN A VIVIPAROUS AFRICAN SKINK AND ITS IMPLICATIONS FOR EVOLUTION AND CONSERVATION 1 2 DANIEL G. BLACKBURN AND ALEXANDER F. FLEMMING 1Department of Biology and Electron Microscopy Facility, Trinity College, Hartford, Connecticut 06106, USA, e-mail: [email protected] 2Department of Botany and Zoology, University of Stellenbosch, Stellenbosch 7600, South Africa Abstract.—Recent research on the African scincid lizard, Trachylepis ivensi, has significantly expanded the range of known reproductive specializations in reptiles. This species is viviparous and exhibits characteristics previously thought to be confined to therian mammals. In most viviparous squamates, females ovulate large yolk-rich eggs that provide most of the nutrients for development. Typically, their placental components (fetal membranes and uterus) are relatively unspecialized, and similar to their oviparous counterparts. In T. ivensi, females ovulate tiny eggs and provide nutrients for embryonic development almost entirely by placental means. Early in gestation, embryonic tissues invade deeply into maternal tissues and establish an intimate “endotheliochorial” relationship with the maternal blood supply by means of a yolk sac placenta. The presence of such an invasive form of implantation in a squamate reptile is unprecedented and has significant functional and evolutionary implications. Discovery of the specializations of T.
    [Show full text]
  • Patterns of Species Richness, Endemism and Environmental Gradients of African Reptiles
    Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Patterns of species richness, endemism ARTICLE and environmental gradients of African reptiles Amir Lewin1*, Anat Feldman1, Aaron M. Bauer2, Jonathan Belmaker1, Donald G. Broadley3†, Laurent Chirio4, Yuval Itescu1, Matthew LeBreton5, Erez Maza1, Danny Meirte6, Zoltan T. Nagy7, Maria Novosolov1, Uri Roll8, 1 9 1 1 Oliver Tallowin , Jean-Francßois Trape , Enav Vidan and Shai Meiri 1Department of Zoology, Tel Aviv University, ABSTRACT 6997801 Tel Aviv, Israel, 2Department of Aim To map and assess the richness patterns of reptiles (and included groups: Biology, Villanova University, Villanova PA 3 amphisbaenians, crocodiles, lizards, snakes and turtles) in Africa, quantify the 19085, USA, Natural History Museum of Zimbabwe, PO Box 240, Bulawayo, overlap in species richness of reptiles (and included groups) with the other ter- Zimbabwe, 4Museum National d’Histoire restrial vertebrate classes, investigate the environmental correlates underlying Naturelle, Department Systematique et these patterns, and evaluate the role of range size on richness patterns. Evolution (Reptiles), ISYEB (Institut Location Africa. Systematique, Evolution, Biodiversite, UMR 7205 CNRS/EPHE/MNHN), Paris, France, Methods We assembled a data set of distributions of all African reptile spe- 5Mosaic, (Environment, Health, Data, cies. We tested the spatial congruence of reptile richness with that of amphib- Technology), BP 35322 Yaounde, Cameroon, ians, birds and mammals. We further tested the relative importance of 6Department of African Biology, Royal temperature, precipitation, elevation range and net primary productivity for Museum for Central Africa, 3080 Tervuren, species richness over two spatial scales (ecoregions and 1° grids). We arranged Belgium, 7Royal Belgian Institute of Natural reptile and vertebrate groups into range-size quartiles in order to evaluate the Sciences, OD Taxonomy and Phylogeny, role of range size in producing richness patterns.
    [Show full text]
  • Squamata, Scincidae) from Pakistan
    ZooKeys 1039: 123–138 (2021) A peer-reviewed open-access journal doi: 10.3897/zookeys.1039.64146 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Out of the blue: The first record of the genus Heremites Gray, 1845 (Squamata, Scincidae) from Pakistan Rafaqat Masroor1, Muhammad Idrees2, Muhammad Khisroon2, Qaisar Jamal2, Daniel Jablonski3 1 Zoological Sciences Division, Pakistan Museum of Natural History, Garden Avenue, Shakarparian, Islama- bad-44000, Pakistan 2 Department of Zoology, University of Peshawar, Peshawar, Pakistan 3 Department of Zoology, Comenius University in Bratislava, Ilkovičova 6, Mlynská dolina, 842 15 Bratislava, Slovakia Corresponding author: Daniel Jablonski ([email protected]) Academic editor: Aaron Bauer | Received 8 February 2021 | Accepted 6 April 2021 | Published 20 May 2021 http://zoobank.org/78118E6B-2FCF-4194-B8AE-F7EEF74F2D6B Citation: Masroor R, Idrees M, Khisroon M, Jamal Q, Jablonski D (2021) Out of the blue: The first record of the genus Heremites Gray, 1845 (Squamata, Scincidae) from Pakistan. ZooKeys 1039: 123–138. https://doi.org/10.3897/ zookeys.1039.64146 Abstract The genus Heremites Gray, 1845 is endemic to the Western Palearctic region, containing morphologi- cally similar species with a not well resolved taxonomy. The genus has a broad distribution from North Africa to Central Asia, with the only known record from northeastern Afghanistan. Three species are currently recognized in the genus with one, H. septemtaeniatus (Reuss, 1834), representing populations at the eastern edge of the genus range. During extensive fieldwork, we discovered H. septemtaeniatus from northwestern Pakistan and provisionally suggest that this population could be morphologically defined as H. septemtaeniatus transcaucasicus (Chernov, 1926).
    [Show full text]
  • Herpetological Survey of Cangandala National Park, with a Synoptic List of the Amphibians and Reptiles of Malanje Province, Central Angola
    408 ARTICLES ———, M.A. BANGOURA, AND W. BÖHME. 2004. The amphibians of the frogs: vocal sac glands of reed frogs (Anura: Hyperoliidae) contain south-eastern Republic of Guinea (Amphibia: Gymnophiona, An- species-specific chemical cocktails. Biol. J. Linn. Soc. 110:828–838. ura). Herpetozoa 17:99–118. ———, P. M. MAIER, W. HÖDL, AND D. PREININGER. 2018. Multimodal sig- ———, K. P. LAMPERT, AND K. E. LINSENMAIR. 2006. Reproductive biol- nal testing reveals gestural tapping behavior in spotted reed frogs. ogy of the West African savannah frog Hyperolius nasutus Günther, Herpetologica 74:127–134. 1864. Herpetozoa 19:3–12. TELFORD, S. R. 1985. Mechanisms of evolution and inter-male spacing SCHICK, S., M. VEITH, AND S. LÖTTERS. 2005. Distribution patterns of amphib- in the painted reedfrog (Hyperolius marmoratus). Anim. Behav. ians from the Kakamega forest, Kenya. Afr. J. Herpetol. 54:185–190. 33:1353–1361. SCHIØTZ A. 1967. The treefrogs (Rhacophoridae) of West Africa. Spolia ———, AND M. L. DYSON. 1988. Some determinants of the mating sys- Zoologica Musei Hauniensis 25:1–346. tem in a population of painted reed frogs (Hyperolius marmora- ———. 1999. Treefrogs of Africa. Edition Chimaira, Frankfurt, Ger- tus). Behaviour 106:265–278. many. 350 pp. ———, ———, AND N. I. PASSMORE. 1989. Mate choice occurs only in SCHMITZ, A., O. EUSKIRCHEN, AND W. BÖHME. 1999. Zur Herpetofauna small choruses of painted reed frogs Hyperolius marmoratus. Bio- einer montanen Regenwaldregion in SW-Kamerun (Mt. Kupe und acoustics 2:47–53. Bakossi-Bergland). I. Einleitung, Bufonidae, und Hyperoliidae. ———, AND N. I. PASSMORE. 1981. Selective phonotaxis of four sympat- Herpetofauna (Weinstadt) 21(121):5–17.
    [Show full text]
  • Captive Wildlife Regulations, 2021, W-13.12 Reg 5
    1 CAPTIVE WILDLIFE, 2021 W-13.12 REG 5 The Captive Wildlife Regulations, 2021 being Chapter W-13.12 Reg 5 (effective June 1, 2021). NOTE: This consolidation is not official. Amendments have been incorporated for convenience of reference and the original statutes and regulations should be consulted for all purposes of interpretation and application of the law. In order to preserve the integrity of the original statutes and regulations, errors that may have appeared are reproduced in this consolidation. 2 W-13.12 REG 5 CAPTIVE WILDLIFE, 2021 Table of Contents PART 1 PART 5 Preliminary Matters Zoo Licences and Travelling Zoo Licences 1 Title 38 Definition for Part 2 Definitions and interpretation 39 CAZA standards 3 Application 40 Requirements – zoo licence or travelling zoo licence PART 2 41 Breeding and release Designations, Prohibitions and Licences PART 6 4 Captive wildlife – designations Wildlife Rehabilitation Licences 5 Prohibition – holding unlisted species in captivity 42 Definitions for Part 6 Prohibition – holding restricted species in captivity 43 Standards for wildlife rehabilitation 7 Captive wildlife licences 44 No property acquired in wildlife held for 8 Licence not required rehabilitation 9 Application for captive wildlife licence 45 Requirements – wildlife rehabilitation licence 10 Renewal 46 Restrictions – wildlife not to be rehabilitated 11 Issuance or renewal of licence on terms and conditions 47 Wildlife rehabilitation practices 12 Licence or renewal term PART 7 Scientific Research Licences 13 Amendment, suspension,
    [Show full text]
  • Rediscovery and Range Extension of the Guinean Skink Trachylepis
    ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Bonn zoological Bulletin - früher Bonner Zoologische Beiträge. Jahr/Year: 2017 Band/Volume: 66 Autor(en)/Author(s): Penner Johannes, Doumbia Joseph, Kouame N'Goran Germain, Chirio Laurent, Sandberger-Loua Laura, Böhme Wolfgang, Barej Michael F. Artikel/Article: Rediscovery and range extension of the Guinean skink Trachylepis keroanensis (Chabanaud, 1921) (Reptilia: Squamata: Scincidae) 55-60 © Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Bonn zoological Bulletin 66 (1): 55–60 April 2017 Rediscovery and range extension of the Guinean skink Trachylepis keroanensis (Chabanaud, 1921) (Reptilia: Squamata: Scincidae) Johannes Penner1,2,*, Joseph Doumbia3, N’Goran Germain Kouamé4, Laurent Chirio5, Laura Sandberger-Loua1, Wolfgang Böhme6 & Michael F. Barej1 1 Museum für Naturkunde, Leibniz Institute Evolution and Biodiversity Science, Invalidenstr. 43, D-10115 Berlin, Germany 2,* Corresponding author: University of Freiburg, Chair of Wildlife Ecology & Management, Tennenbacher Str. 4, D-79106 Freiburg, Germany; [email protected] 3 Envisud Guinée; Quartier: Kipé T2 commune de Ratoma; 030BP:558 Conakry; République de Guinée 4 Jean Lorougnon Guédé University, UFR-Environment, Department of Biology & Animal Physiology, Daloa, BP 150, Côte d’Ivoire 5 P.O. Box 87811, Riyadh 11652, Saudi Arabia 6 Zoologisches Forschungsmuseum Alexander Koenig,
    [Show full text]
  • DNA Barcoding Assessment of Genetic Variation in Two Widespread Skinks from Madagascar, Trachylepis Elegans and T
    Zootaxa 3755 (5): 477–484 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3755.5.7 http://zoobank.org/urn:lsid:zoobank.org:pub:039C3026-D3B9-47B2-8340-6B916C636665 DNA barcoding assessment of genetic variation in two widespread skinks from Madagascar, Trachylepis elegans and T. gravenhorstii (Squamata: Scincidae) MIGUEL VENCES1,6*, ALEXANDRA LIMA2,3*, AURÉLIEN MIRALLES4 & FRANK GLAW5 1Zoological Institute, Technische Universität Braunschweig, Mendelssohnstr. 4, 38106 Braunschweig, Germany 2Centro de Investigação em Biodiversidade e Recursos Genéticos (CIBIO), Campus Agrário de Vairão, R. Padre Armando Quintas, 4485-661 Vairão, Portugal 3Departamento de Biologia, Faculdade de Ciências, Universidade do Porto, R. Campo Alegre s/n, 4169-007 Porto, Portugal 4CNRS-UMR5175 Centre d'Ecologie Fonctionnelle et Evolutive, 1919 route de Mende, 34293 Montpellier cedex 5, France 5Zoologische Staatssammlung München, Münchhausenstr. 21, 81247 München, Germany 6Corresponding author. E-mail: [email protected] *These authors contributed equally to the paper Abstract Trachylepis elegans and T. gravenhorstii are two of the most widespread reptiles in Madagascar, inhabiting a wide variety of habitats. Previous studies have indicated a considerable mitochondrial DNA (mtDNA) variation within these species, but the geographic distribution of the major haplotype lineages is poorly known. Herein we analyse the phylogeography of these lizards based on 107 sequences of the mitochondrial cytochrome oxidase subunit I gene, 101 of which newly de- termined. As in previous mtDNA assessments, T. elegans and T. gravenhorstii were not reciprocally monophyletic, al- though recent analyses including nuclear markers indicated their probable monophyly, respectively.
    [Show full text]