Mana Island Ecological Restoration Plan
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Nyika and Vwaza Reptiles & Amphibians Checklist
LIST OF REPTILES AND AMPHIBIANS OF NYIKA NATIONAL PARK AND VWAZA MARSH WILDLIFE RESERVE This checklist of all reptile and amphibian species recorded from the Nyika National Park and immediate surrounds (both in Malawi and Zambia) and from the Vwaza Marsh Wildlife Reserve was compiled by Dr Donald Broadley of the Natural History Museum of Zimbabwe in Bulawayo, Zimbabwe, in November 2013. It is arranged in zoological order by scientific name; common names are given in brackets. The notes indicate where are the records are from. Endemic species (that is species only known from this area) are indicated by an E before the scientific name. Further details of names and the sources of the records are available on request from the Nyika Vwaza Trust Secretariat. REPTILES TORTOISES & TERRAPINS Family Pelomedusidae Pelusios rhodesianus (Variable Hinged Terrapin) Vwaza LIZARDS Family Agamidae Acanthocercus branchi (Branch's Tree Agama) Nyika Agama kirkii kirkii (Kirk's Rock Agama) Vwaza Agama armata (Eastern Spiny Agama) Nyika Family Chamaeleonidae Rhampholeon nchisiensis (Nchisi Pygmy Chameleon) Nyika Chamaeleo dilepis (Common Flap-necked Chameleon) Nyika(Nchenachena), Vwaza Trioceros goetzei nyikae (Nyika Whistling Chameleon) Nyika(Nchenachena) Trioceros incornutus (Ukinga Hornless Chameleon) Nyika Family Gekkonidae Lygodactylus angularis (Angle-throated Dwarf Gecko) Nyika Lygodactylus capensis (Cape Dwarf Gecko) Nyika(Nchenachena), Vwaza Hemidactylus mabouia (Tropical House Gecko) Nyika Family Scincidae Trachylepis varia (Variable Skink) Nyika, -
Alpine Skinks
AUSTRALIAN THREATENED SPECIES ALPINE SKINKS Alpine Water Skink Eulamprus kosciuskoi; Conservation Status (Victoria): Critically Endangered* Alpine She-oak Skink Cyclodomorphus praealtus ; Conservation Status (Victoria): Endangered* *Advisory List of Rare or Threatened Vertebrate Fauna, Department of Sustainability and Environment (2003) and listed under Flora and Fauna Guarantee Act 1988 What do they look like? Australia and its external territories occur nowhere else in the world. Generally, skinks (family Scincidae ) are small- • to medium-sized lizards. The reptile fauna of the alpine region of Victoria is dominated by skinks (in terms of Two threatened alpine skinks are the Alpine she- numbers), although one dragon lizard and oak skink — a relatively broad-headed, short- three venomous snakes also occur in this legged, smooth-scaled lizard and the Alpine area. • water skink – a robust skink, with a body length Two other Victorian alpine skinks, the of up to 80 millimetres. Alpine bog skink ( Pseudemoia cryodroma) and the Guthega skink ( Egernia guthega) are also threatened with extinction in Where do they live? Victoria. Although some alpine skink species also occur in • The Alpine skinks give birth to live young. other parts of Victoria, several are endemic to the • A large proportion of the known range of the Alps. Nearly half of the skinks are officially Alpine she-oak skink occurs within, or listed as threatened by the Victorian Department adjacent to, the Mt Hotham and Falls Creek of Sustainability and Environment. Some of Alpine Resorts. these reptiles are abundant and readily observed, whilst others are rare and/or secretive. The Alpine water skink is restricted to sphagnum bogs, streamsides and wet heath vegetation. -
Plant Section Introduction
Re-introduction Practitioners Directory - 1998 RE-INTRODUCTION PRACTITIONERS DIRECTORY 1998 Compiled and Edited by Pritpal S. Soorae and Philip J. Seddon Re-introduction Practitioners Directory - 1998 © National Commission for Wildlife Conservation and Development, 1998 Printing and Publication details Legal Deposit no. 2218/9 ISBN: 9960-614-08-5 Re-introduction Practitioners Directory - 1998 Copies of this directory are available from: The Secretary General National Commission for Wildlife Conservation and Development Post Box 61681, Riyadh 11575 Kingdom of Saudi Arabia Phone: +966-1-441-8700 Fax: +966-1-441-0797 Bibliographic Citation: Soorae, P. S. and Seddon, P. J. (Eds). 1998. Re-introduction Practitioners Directory. Published jointly by the IUCN Species Survival Commission’s Re-introduction Specialist Group, Nairobi, Kenya, and the National Commission for Wildlife Conservation and Development, Riyadh, Saudi Arabia. 97pp. Cover Photo: Arabian Oryx Oryx leucoryx (NWRC Photo Library) Re-introduction Practitioners Directory - 1998 CONTENTS FOREWORD Professor Abdulaziz Abuzinadai PREFACE INTRODUCTION Dr Mark Stanley Price USING THE DIRECTORY ACKNOWLEDGEMENTS PART A. ANIMALS I MOLLUSCS 1. GASTROPODS 1.1 Cittarium pica Top Shell 1.2 Placostylus ambagiosus Flax Snail 1.3 Placostylus ambagiosus Land Snail 1.4 Partula suturalis 1.5 Partula taeniata 1.6 Partula tahieana 1.7 Partula tohiveana 2. BIVALVES 2.1 Freshwater Mussels 2.2 Tridacna gigas Giant Clam II ARTHROPODS 3. ORTHOPTERA 3.1 Deinacrida sp. Weta 3.2 Deinacrida rugosa/parva Cook’s Strait Giant Weta Re-introduction Practitioners Directory - 1998 3.3 Gryllus campestris Field Cricket 4. LEPIDOPTERA 4.1 Carterocephalus palaemon Chequered Skipper 4.2 Lycaena dispar batavus Large Copper 4.3 Lycaena helle 4.4 Lycaeides melissa 4.5 Papilio aristodemus ponoceanus Schaus Swallowtail 5. -
Care Sheet: Robust and Mcgregor's Skinks
Care Sheet: Robust and McGregor’s skinks Robust skink (Oligosoma alani) McGregor’s skink (Oligosoma macgregori) Adult Size: up to 150mm SVL. Adult Size: up to 114mm SVL. Threat status: ‘At Risk – Recovering’. Threat status: ‘At Risk – Recovering’. Lifespan: over 32 years. (likely over 40). Lifespan: over 35 years. Habitat: coastal forest, flaxland, deep rock Habitat: coastal forest, flaxland, boulder beaches, piles, iceplant herbfield, seabird burrows, deep deep rock piles, iceplant herbfield, seabird burrows, leaf litter and under rocks / logs. deep leaf litter and under rocks / logs. Permit Level: Conservation species. Permit Level: Insurance population species. Enclosure: Minimum recommended enclosure size = 150x70x70cm (LxWxH). Ideal Group Size: 1:1 (M:F). Compatible Species: Duvaucel’s geckos (but authorisations usually prohibit housing with other species). Recommended Cage Furnishing: The enclosure should be decorated with live plants (though these are not entirely necessary), logs, low branches for climbing, and a thick layer of leaf litter for these skinks to forage and take refuge in. Robust and McGregor’s skinks are particularly susceptible to evaporative water loss through their skin, so it is crucial that they be provided adequate damp refuge sites in the form of buried containers filled with damp leaf litter and/or damp sphagnum moss. The provision of dry refuges is also equally important as despite these lizards’ requirement for damp habitats, they will usually take refuge in cool dry refuges. Issues with skin infections can be experienced if these species are kept in conditions that are too damp where they aren’t provided adequate dry refuge sites. Refuge sites that have proved popular in captivity include rock piles, sections of bamboo or polythene pipe (with one end blocked up) buried in leaf litter, rock piles, bark stacks, hollow ponga logs, and stacks of Onduline semi-buried in leaf litter. -
Reptile Fauna of the Chancani Reserve
©Österreichische Gesellschaft für Herpetologie e.V., Wien, Austria, download unter www.biologiezentrum.at SHORT NOTE HERPETOZOA 19(1/2) Wien, 30. Juli 2006 SHORT NOTE 85 tofauna of Round Island, Mauritius.- Biota, Race; 3(1- snake species (four families). Teius teyou 2): 77-84. PouGH, F. H. & ANDREWS, R. M. & CADLE, and Stenocercus doellojuradoi (lizards), and J. E. & CRUMP, M. L. & SAVITZKY, A. H & WELLS, K. D. (2004): Herpetology, third edition. Upper Saddle River Waglerophis merremi, Micrurus pyrrho- (Pearson, Prentice Hall), 726 pp. STAUB, F. (1993): cryptus and Crotalus durissus terrificus Fauna of Mauritius and associated flora. Port Louis, (snakes) were the most abundant species in Mauritius (Précigraph Ltd.), 97 pp.. each group (table 1). Field observations KEYWORDS: Reptilia: Squamata: Bolyeriidae, added three lizards (Tropidurus spinulosus, Bolyeria multocarinata; reproduction, eggs, additional newly discovered specimen, morphology, pholidosis Liolaemus sp. aff. gracilis and Vanzosaura rubricando) and one snake species {Boa SUBMITTED: May 20, 2005 constrictor occidentalis) and bibliographic AUTHORS: Dr. Jakob HALLERMANN, Biozent- rum Grindel und Zoologisches Museum Hamburg, sources added one turtle and one snake Martin-Luther-King-Platz 3, 20146 Hamburg, Germany species (table 1). < [email protected] >; Dr. Frank GLAW, Zo- We assigned the conservation status ologische Staatssammlung München, Münchhausen- categories provided by Secretarla de Ambi- straße 21, 81247 München, Germany < Frank.Glaw@ zsm.mwn.de > ente y Desarrollo Sustentable - Ministerio de Salud y Ambiente (2004). Accordingly, the lizard fauna of the Chancani Reserve Reptile fauna of the Chancani includes two species considered as "vulner- Reserve (Arid Chaco, Argentina): able" (Cnemidophorus serranus and Leio- species list and conservation status saurus paronae, and one Chaco endemic species (Stenocercus doellojuradoi) (LEY- The Chancani Provincial Reserve NAUD & BÛCHER 2005). -
Ecosystem Disturbance and Wildlife Conservation in Western Grasslands
Evolution and management of the North American grassland herpetofauna Norman J. Scott, Jr.1 Abstract.—The modern North American grassland herpetofauna has evolved in situ since the Miocene. Pleistocene glaciation had a minimal effect except in the far North, with only minor displacements of some species. South of the glaciers, winters were warmer and summers cooler than at present. Snake- like reptiles, leaping frogs, and turtle “tanks” are favored adaptive types in uniform dense grassland. A typical fauna consists of about 10-15 species, mostly snakes. Special habitat components, such as streams and ponds, bare ground, sand, trees, prairie dog towns, and rocky outcrops, add distinct suites of species. There is also an increase in species number from north to south and west to east. Grassland use and management, such as prairie dog con- trol, off-road vehicle traffic, and brush removal, have demonstrable effects on the herpetofauna. However, the effects of three of the most widespread management procedures—water development, grazing, and fire—are largely unstudied. Although highly fragmented, the majority of species of grassland reptiles and amphibians are widespread and populations are resilient, but there are special conservation problems associated with Pleistocene relicts with limited distributions. INTRODUCTION Parmenter et al. (1994) documented the excep- tionally high vertebrate diversity in southwestern At the time of the arrival of Europeans in North rangelands, and they emphasized that preserva- America, much of the interior of the continent was tion of this biodiversity in the remaining habitat covered by grasslands. The heart of this great fragments will depend on skillful management of expanse was the tallgrass prairie of the human activities in a fashion that integrates faunal midwestern United States. -
The Conservation Status of the World's Reptiles
Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications Biological Sciences, Department of 1-2013 The Conservation Status of the World’s Reptiles Tony Gamble Follow this and additional works at: https://epublications.marquette.edu/bio_fac Part of the Biology Commons Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications/College of Arts and Sciences This paper is NOT THE PUBLISHED VERSION; but the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation below. Biological Conservation, Vol. 157, (January 2013): 372-385. DOI. This article is © Elsevier and permission has been granted for this version to appear in e-Publications@Marquette. Elsevier does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from Elsevier. The Conservation Status of the World’s Reptiles Monika Böhm Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Ben Collen Institute of Zoology, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Jonathan E.M. Baillie Conservation Programmes, Zoological Society of London, Regent’s Park, London NW1 4RY, UK Philip Bowles IUCN – CI Biodiversity Assessment Unit, Conservation International, 2011 Crystal Drive Ste 500, Arlington, VA Janice Chanson Species Programme, IUCN, Rue Mauverney 28, 1196 Gland, Switzerland IUCN – CI Biodiversity Assessment Unit, c/o 130 Weatherall Road, Cheltenham 3192, Vic., Australia Neil Cox IUCN – CI Biodiversity Assessment Unit, Conservation International, 2011 Crystal Drive Ste 500, Arlington, VA Species Programme, IUCN, Rue Mauverney 28, 1196 Gland, Switzerland Geoffrey Hammerson NatureServe, 746 Middlepoint Road, Port Townsend, WA Michael Hoffmann IUCN SSC Species Survival Commission, c/o United Nations Environment Programme World Conservation Monitoring Centre, 219 Huntingdon Road, Cambridge CB3 0DL, UK Suzanne R. -
Recovery Plan for Whitaker's Skink and Robust Skink
RECOVERY PLAN FOR WHITAKER'S SKINK AND ROBUST SKINK Prepared by David Towns (Science and Research Division) for Threatened Species Unit, Wellington Department of Conservation P.O. Box 10-420 Wellington NEW ZEALAND May 1992 ISSN 1170-3806 ISBN 0-478-01382-5 Threatened Species Recovery Plan Series No. 3 FOREWORD This recovery plan is one of a series of Threatened Species Unit publications produced by the Department of Conservation. Recovery plans are statements of the department's intentions for the conservation of plants and animals for a defined period. In focusing on goals and objectives for research and management, and the tasks by which these will be achieved, recovery plans serve to guide the department in its allocation of resources. Following the preparation of a technical report which was refined by scientists and managers within the department a draft of this plan was forwarded to the N. Z. Conservation Authority and relevant Conservation Boards and other interest groups for comment. After further refinement this plan was formally approved by the Director- General of Conservation on 1 April 1992. The department acknowledges the need to take into account the views of the tangata whenua and the application of their values in the conservation of natural resources. As the expression of these values may vary between iwi, it is not possible to incorporate these variations within a general theme in all recovery plans. This recovery plan will be refined and implemented in such a way as to ensure that consultation with tangata whenua of the areas in which Whitaker's and robust skinks are present has been carried out. -
Recovery Plan for Whitaker's Skink and Robust Skink
18 Increase the number of Whitaker's and robust skinks in captivity so that self-sustaining populations can be established for later release. 6. Protect populations on land outside Crown control. Establish management partnerships on locations in private ownership to ensure that their natural values as key sites for threatened lizards are not compromised. 7. Manage the mainland population of Whitaker's skink at Pukerua Bay. Establish a formally gazetted reserve at Pukerua Bay and institute management that will enhance the Whitaker's skink population. 8. Promote public interest and involvement in the recovery of Whitaker's skink and robust skink and in community restoration. Keep the public informed of progress with habitat restoration, and lizard reintroductions, involve interested groups as appropriate and provide for long term public participation. CRITICAL PATH 19 8. RECOVERY STRATEGY: WORK PLAN To meet each objective and the fulfil the recovery goals the following actions are required: OBJECTIVE 1. ERADICATE RODENTS FROM LARGE ISLANDS Explanation Restoration of island biotic communities relies on efficient techniques for eradication of rodents. Successful cost-effective techniques have been developed for small islands, but these tend to be labour intensive (McFadden and Towns 1991). Mechanical techniques for air drops of rodenticide will need to be applied to islands of 100 ha or more if the options defined in this plan are to be met. Plan Aerial drops by helicopter using TALON 20P provided gratis by a chemical company began in September 1991 on Stanley Island (100 ha). If successful it may be extended to Red Mercury Island in 1992. Outcomes The eradication campaign against kiore (as well as rabbits) on Stanley and Red Mercury Islands will: Rehabilitate two populations of tuatara Release invertebrates from predation by kiore Provide two very large islands with considerable suitable habitat for Whitaker's and robust skinks. -
Notice Warning Concerning Copyright Restrictions P.O
Publisher of Journal of Herpetology, Herpetological Review, Herpetological Circulars, Catalogue of American Amphibians and Reptiles, and three series of books, Facsimile Reprints in Herpetology, Contributions to Herpetology, and Herpetological Conservation Officers and Editors for 2015-2016 President AARON BAUER Department of Biology Villanova University Villanova, PA 19085, USA President-Elect RICK SHINE School of Biological Sciences University of Sydney Sydney, AUSTRALIA Secretary MARION PREEST Keck Science Department The Claremont Colleges Claremont, CA 91711, USA Treasurer ANN PATERSON Department of Natural Science Williams Baptist College Walnut Ridge, AR 72476, USA Publications Secretary BRECK BARTHOLOMEW Notice warning concerning copyright restrictions P.O. Box 58517 Salt Lake City, UT 84158, USA Immediate Past-President ROBERT ALDRIDGE Saint Louis University St Louis, MO 63013, USA Directors (Class and Category) ROBIN ANDREWS (2018 R) Virginia Polytechnic and State University, USA FRANK BURBRINK (2016 R) College of Staten Island, USA ALISON CREE (2016 Non-US) University of Otago, NEW ZEALAND TONY GAMBLE (2018 Mem. at-Large) University of Minnesota, USA LISA HAZARD (2016 R) Montclair State University, USA KIM LOVICH (2018 Cons) San Diego Zoo Global, USA EMILY TAYLOR (2018 R) California Polytechnic State University, USA GREGORY WATKINS-COLWELL (2016 R) Yale Peabody Mus. of Nat. Hist., USA Trustee GEORGE PISANI University of Kansas, USA Journal of Herpetology PAUL BARTELT, Co-Editor Waldorf College Forest City, IA 50436, USA TIFFANY -
References for Life History
Literature Cited Adler, K. 1979. A brief history of herpetology in North America before 1900. Soc. Study Amphib. Rept., Herpetol. Cir. 8:1-40. 1989. Herpetologists of the past. In K. Adler (ed.). Contributions to the History of Herpetology, pp. 5-141. Soc. Study Amphib. Rept., Contrib. Herpetol. no. 5. Agassiz, L. 1857. Contributions to the Natural History of the United States of America. 2 Vols. Little, Brown and Co., Boston. 452 pp. Albers, P. H., L. Sileo, and B. M. Mulhern. 1986. Effects of environmental contaminants on snapping turtles of a tidal wetland. Arch. Environ. Contam. Toxicol, 15:39-49. Aldridge, R. D. 1992. Oviductal anatomy and seasonal sperm storage in the southeastern crowned snake (Tantilla coronata). Copeia 1992:1103-1106. Aldridge, R. D., J. J. Greenshaw, and M. V. Plummer. 1990. The male reproductive cycle of the rough green snake (Opheodrys aestivus). Amphibia-Reptilia 11:165-172. Aldridge, R. D., and R. D. Semlitsch. 1992a. Female reproductive biology of the southeastern crowned snake (Tantilla coronata). Amphibia-Reptilia 13:209-218. 1992b. Male reproductive biology of the southeastern crowned snake (Tantilla coronata). Amphibia-Reptilia 13:219-225. Alexander, M. M. 1943. Food habits of the snapping turtle in Connecticut. J. Wildl. Manag. 7:278-282. Allard, H. A. 1945. A color variant of the eastern worm snake. Copeia 1945:42. 1948. The eastern box turtle and its behavior. J. Tenn. Acad. Sci. 23:307-321. Allen, W. H. 1988. Biocultural restoration of a tropical forest. Bioscience 38:156-161. Anonymous. 1961. Albinism in southeastern snakes. Virginia Herpetol. Soc. Bull. -
RI DEM/Agriculture- Rules and Regulations Governing Importation
STATE OF RHODE ISLAND AND PROVIDENCE PLANTATIONS, DEPARTMENT OF ENVIRONMENTAL MANAGEMENT, DIVISION OF AGRICULTURE RULES AND REGULATIONS GOVERNING IMPORTATION AND POSSESSION OF EXOTIC WILD ANIMALS Effective April 2010 AUTHORITY: These regulations are authorized pursuant to R.I. Gen. Laws § 42-17.1-2(19) and Chapter 4-18 as amended, and have been promulgated pursuant to the procedures set forth in the R.I. Administrative Procedures Act, R.I. Gen. Laws Chapter 42-35. 1 TABLE OF CONTENTS: RULE 1. PURPOSE RULE 2. AUTHORITY RULE 3. APPLICATION RULE 4. DEFINITIONS RULE 5. REQUIREMENTS RULE 6. ISSUANCE AND CONDITIONS RULE 7. EXEMPTIONS RULE 8. VIOLATIONS RULE 9. APPEAL AND HEARING PROCEDURE RULE 10. SEVERABILITY RULE 11. SUPERSEDED RULES AND REGULATIONS RULE 12. EFFECTIVE DATE RULE 1. PURPOSE: 1. To permit importation and possession within Rhode Island of those exotic animals that are free of diseases that pose a threat to humans, livestock and other domesticated animals, and native wildlife. 2. To allow importation/possession by only those persons who can demonstrate that they have adequate facilities and adequate knowledge of animal health and husbandry to ensure both public safety as well as the health and well-being of the imported/possessed exotic animal. 3. To ensure that endangered and threatened species are not imported/possessed in Rhode Island without a permit. RULE 2. AUTHORITY: These Rules and Regulations are promulgated pursuant to Chapter 42-17.1, Environmental Management, and Section 4-18-9, and in accordance with 42-35, Administrative Procedures, of the Rhode Island General Laws of 1956, as amended.