Captive Care of the Desert Tortoise, Gopherus Agassizii Jay D
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§4-71-6.5 LIST of CONDITIONALLY APPROVED ANIMALS November
§4-71-6.5 LIST OF CONDITIONALLY APPROVED ANIMALS November 28, 2006 SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Plesiopora FAMILY Tubificidae Tubifex (all species in genus) worm, tubifex PHYLUM Arthropoda CLASS Crustacea ORDER Anostraca FAMILY Artemiidae Artemia (all species in genus) shrimp, brine ORDER Cladocera FAMILY Daphnidae Daphnia (all species in genus) flea, water ORDER Decapoda FAMILY Atelecyclidae Erimacrus isenbeckii crab, horsehair FAMILY Cancridae Cancer antennarius crab, California rock Cancer anthonyi crab, yellowstone Cancer borealis crab, Jonah Cancer magister crab, dungeness Cancer productus crab, rock (red) FAMILY Geryonidae Geryon affinis crab, golden FAMILY Lithodidae Paralithodes camtschatica crab, Alaskan king FAMILY Majidae Chionocetes bairdi crab, snow Chionocetes opilio crab, snow 1 CONDITIONAL ANIMAL LIST §4-71-6.5 SCIENTIFIC NAME COMMON NAME Chionocetes tanneri crab, snow FAMILY Nephropidae Homarus (all species in genus) lobster, true FAMILY Palaemonidae Macrobrachium lar shrimp, freshwater Macrobrachium rosenbergi prawn, giant long-legged FAMILY Palinuridae Jasus (all species in genus) crayfish, saltwater; lobster Panulirus argus lobster, Atlantic spiny Panulirus longipes femoristriga crayfish, saltwater Panulirus pencillatus lobster, spiny FAMILY Portunidae Callinectes sapidus crab, blue Scylla serrata crab, Samoan; serrate, swimming FAMILY Raninidae Ranina ranina crab, spanner; red frog, Hawaiian CLASS Insecta ORDER Coleoptera FAMILY Tenebrionidae Tenebrio molitor mealworm, -
Egyptian Tortoise (Testudo Kleinmanni)
EAZA Reptile Taxon Advisory Group Best Practice Guidelines for the Egyptian tortoise (Testudo kleinmanni) First edition, May 2019 Editors: Mark de Boer, Lotte Jansen & Job Stumpel EAZA Reptile TAG chair: Ivan Rehak, Prague Zoo. EAZA Best Practice Guidelines Egyptian tortoise (Testudo kleinmanni) EAZA Best Practice Guidelines disclaimer Copyright (May 2019) by EAZA Executive Office, Amsterdam. All rights reserved. No part of this publication may be reproduced in hard copy, machine-readable or other forms without advance written permission from the European Association of Zoos and Aquaria (EAZA). Members of the European Association of Zoos and Aquaria (EAZA) may copy this information for their own use as needed. The information contained in these EAZA Best Practice Guidelines has been obtained from numerous sources believed to be reliable. EAZA and the EAZA Reptile TAG make a diligent effort to provide a complete and accurate representation of the data in its reports, publications, and services. However, EAZA does not guarantee the accuracy, adequacy, or completeness of any information. EAZA disclaims all liability for errors or omissions that may exist and shall not be liable for any incidental, consequential, or other damages (whether resulting from negligence or otherwise) including, without limitation, exemplary damages or lost profits arising out of or in connection with the use of this publication. Because the technical information provided in the EAZA Best Practice Guidelines can easily be misread or misinterpreted unless properly analysed, EAZA strongly recommends that users of this information consult with the editors in all matters related to data analysis and interpretation. EAZA Preamble Right from the very beginning it has been the concern of EAZA and the EEPs to encourage and promote the highest possible standards for husbandry of zoo and aquarium animals. -
Manual for the Differentiation of Captive-Produced and Wild-Caught Turtles and Tortoises (Testudines)
Image: Peter Paul van Dijk Image:Henrik Bringsøe Image: Henrik Bringsøe Image: Andrei Daniel Mihalca Image: Beate Pfau MANUAL F O R T H E DIFFERENTIATION OF CAPTIVE-PRODUCED AND WILD-CAUGHT TURTLES AND TORTOISES (TESTUDINES) PREPARED BY SPECIES360 UNDER CONTRACT FOR THE CITES SECRETARIAT Manual for the differentiation of captive-produced and wild-caught turtles and tortoises (Testudines) This document was prepared by Species360 under contract for the CITES Secretariat. Principal Investigators: Prof. Dalia A. Conde, Ph.D. and Johanna Staerk, Ph.D., Species360 Conservation Science Alliance, https://www.species360.orG Authors: Johanna Staerk1,2, A. Rita da Silva1,2, Lionel Jouvet 1,2, Peter Paul van Dijk3,4,5, Beate Pfau5, Ioanna Alexiadou1,2 and Dalia A. Conde 1,2 Affiliations: 1 Species360 Conservation Science Alliance, www.species360.orG,2 Center on Population Dynamics (CPop), Department of Biology, University of Southern Denmark, Denmark, 3 The Turtle Conservancy, www.turtleconservancy.orG , 4 Global Wildlife Conservation, globalwildlife.orG , 5 IUCN SSC Tortoise & Freshwater Turtle Specialist Group, www.iucn-tftsG.org. 6 Deutsche Gesellschaft für HerpetoloGie und Terrarienkunde (DGHT) Images (title page): First row, left: Mixed species shipment (imaGe taken by Peter Paul van Dijk) First row, riGht: Wild Testudo marginata from Greece with damaGe of the plastron (imaGe taken by Henrik BrinGsøe) Second row, left: Wild Testudo marginata from Greece with minor damaGe of the carapace (imaGe taken by Henrik BrinGsøe) Second row, middle: Ticks on tortoise shell (Amblyomma sp. in Geochelone pardalis) (imaGe taken by Andrei Daniel Mihalca) Second row, riGht: Testudo graeca with doG bite marks (imaGe taken by Beate Pfau) Acknowledgements: The development of this manual would not have been possible without the help, support and guidance of many people. -
The Conservation Biology of Tortoises
The Conservation Biology of Tortoises Edited by Ian R. Swingland and Michael W. Klemens IUCN/SSC Tortoise and Freshwater Turtle Specialist Group and The Durrell Institute of Conservation and Ecology Occasional Papers of the IUCN Species Survival Commission (SSC) No. 5 IUCN—The World Conservation Union IUCN Species Survival Commission Role of the SSC 3. To cooperate with the World Conservation Monitoring Centre (WCMC) The Species Survival Commission (SSC) is IUCN's primary source of the in developing and evaluating a data base on the status of and trade in wild scientific and technical information required for the maintenance of biological flora and fauna, and to provide policy guidance to WCMC. diversity through the conservation of endangered and vulnerable species of 4. To provide advice, information, and expertise to the Secretariat of the fauna and flora, whilst recommending and promoting measures for their con- Convention on International Trade in Endangered Species of Wild Fauna servation, and for the management of other species of conservation concern. and Flora (CITES) and other international agreements affecting conser- Its objective is to mobilize action to prevent the extinction of species, sub- vation of species or biological diversity. species, and discrete populations of fauna and flora, thereby not only maintain- 5. To carry out specific tasks on behalf of the Union, including: ing biological diversity but improving the status of endangered and vulnerable species. • coordination of a programme of activities for the conservation of biological diversity within the framework of the IUCN Conserva- tion Programme. Objectives of the SSC • promotion of the maintenance of biological diversity by monitor- 1. -
University of Nevada, Reno Effects of Fire on Desert Tortoise (Gopherus Agassizii) Thermal Ecology a Dissertation Submitted in P
University of Nevada, Reno Effects of fire on desert tortoise (Gopherus agassizii) thermal ecology A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Ecology, Evolution, and Conservation Biology by Sarah J. Snyder Dr. C. Richard Tracy/Dissertation Advisor May 2014 THE GRADUATE SCHOOL We recommend that the dissertation prepared under our supervision by SARAH J. SNYDER Entitled Effects of fire on desert tortoise (Gopherus agassizii) thermal ecology be accepted in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY C. Richard Tracy, Ph.D., Advisor Kenneth Nussear, Ph.D., Committee Member Peter Weisberg, Ph.D., Committee Member Lynn Zimmerman, Ph.D., Committee Member Lesley DeFalco, Ph.D., Graduate School Representative David W. Zeh, Ph. D., Dean, Graduate School May, 2014 i ABSTRACT Among the many threats facing the desert tortoise (Gopherus agassizii) is the destruction and alteration of habitat. In recent years, wildfires have burned extensive portions of tortoise habitat in the Mojave Desert, leaving burned landscapes that are virtually devoid of living vegetation. Here, we investigated the effects of fire on the thermal ecology of the desert tortoise by quantifying the thermal quality of above- and below-ground habitat, determining which shrub species are most thermally valuable for tortoises including which shrub species are used by tortoises most frequently, and comparing the body temperature of tortoises in burned and unburned habitat. To address these questions we placed operative temperature models in microhabitats that received filtered radiation to test the validity of assuming that the interaction between radiation and radiation-absorbing properties of the model can result in a single, mean radiant absorptance regardless of whether the incident solar radiation is direct unfiltered or filtered by plant canopies, using the desert tortoise as a case study. -
Indian Star Tortoise Care
RVC Exotics Service Royal Veterinary College Royal College Street London NW1 0TU T: 0207 554 3528 F: 0207 388 8124 www.rvc.ac.uk/BSAH INDIAN STAR TORTOISE CARE Indian star tortoises originate from the semi-arid dry grasslands of Indian subcontinent. They can be easily recognised by the distinctive star pattern on their bumpy carapace. Star tortoises are very sensitive to their environmental conditions and so not recommended for novice tortoise owners. It is important to note that these tortoises do not hibernate. HOUSING • Tortoises make poor vivarium subjects. Ideally a floor pen or tortoise table should be created. This needs to have solid sides (1 foot high) for most tortoises. Many are made out of wood or plastic. A large an area as possible should be provided, but as the size increases extra basking sites will need to be provided. For a small juvenile at least 90 cm (3 feet) long x 30 cm (1 foot) wide is recommended. This is required to enable a thermal gradient to be created along the length of the tank (hot to cold). • Hides are required to provide some security. Artificial plants, cardboard boxes, plant pots, logs or commercially available hides can be used. They should be placed both at the warm and cooler ends of the tank. • Substrates suitable for housing tortoises include newspaper, Astroturf, and some of the commercially available substrates. Natural substrate such as soil may also be used to allow for digging. It is important that the substrates either cannot be eaten, or if they are, do not cause blockages as this can prove fatal. -
Aldabrachelys Arnoldi (Bour 1982) – Arnold's Giant Tortoise
Conservation Biology of Freshwater Turtles and Tortoises: A Compilation ProjectTestudinidae of the IUCN/SSC — AldabrachelysTortoise and Freshwater arnoldi Turtle Specialist Group 028.1 A.G.J. Rhodin, P.C.H. Pritchard, P.P. van Dijk, R.A. Saumure, K.A. Buhlmann, J.B. Iverson, and R.A. Mittermeier, Eds. Chelonian Research Monographs (ISSN 1088-7105) No. 5, doi:10.3854/crm.5.028.arnoldi.v1.2009 © 2009 by Chelonian Research Foundation • Published 18 October 2009 Aldabrachelys arnoldi (Bour 1982) – Arnold’s Giant Tortoise JUSTIN GERLACH 1 1133 Cherry Hinton Road, Cambridge CB1 7BX, United Kingdom [[email protected]] SUMMARY . – Arnold’s giant tortoise, Aldabrachelys arnoldi (= Dipsochelys arnoldi) (Family Testudinidae), from the granitic Seychelles, is a controversial species possibly distinct from the Aldabra giant tortoise, A. gigantea (= D. dussumieri of some authors). The species is a morphologi- cally distinctive morphotype, but has so far not been genetically distinguishable from the Aldabra tortoise, and is considered synonymous with that species by many researchers. Captive reared juveniles suggest that there may be a genetic basis for the morphotype and more detailed genetic work is needed to elucidate these relationships. The species is the only living saddle-backed tortoise in the Seychelles islands. It was apparently extirpated from the wild in the 1800s and believed to be extinct until recently purportedly rediscovered in captivity. The current population of this morphotype is 23 adults, including 18 captive adult males on Mahé Island, 5 adults recently in- troduced to Silhouette Island, and one free-ranging female on Cousine Island. Successful captive breeding has produced 138 juveniles to date. -
Seychelles Giant Tortoise
Conservation Biology of Freshwater Turtles and Tortoises: A Compilation ProjectTestudinidae of the IUCN/SSC — Aldabrachelys Tortoise and Freshwater hololissa Turtle Specialist Group 061.1 A.G.J. Rhodin, P.C.H. Pritchard, P.P. van Dijk, R.A. Saumure, K.A. Buhlmann, J.B. Iverson, and R.A. Mittermeier, Eds. Chelonian Research Monographs (ISSN 1088-7105) No. 5, doi:10.3854/crm.5.061.hololissa.v1.2011 © 2011 by Chelonian Research Foundation • Published 31 December 2011 Aldabrachelys hololissa (Günther 1877) – Seychelles Giant Tortoise JUSTIN GERLACH 1 1133 Cherry Hinton Road, Cambridge, CB1 7BX United Kingdom [[email protected]] SUMMARY . – The Seychelles Giant Tortoise, Aldabrachelys hololissa (= Dipsochelys hololissa) (Family Testudinidae) is a controversial species possibly distinct from the Aldabra giant tor- toise, A. gigantea (= D. dussumieri of some authors). The species is a morphologically distinctive morphotype, but has so far not been genetically distinguishable from the Aldabra tortoise, and is considered by many researchers to be either synonymous with or only subspecifically distinct from that taxon. It is a domed grazing species, differing from the Aldabra tortoise in its broader shape and reduced ossification of the skeleton; it differs also from the other controversial giant tortoise in the Seychelles, the saddle-backed morphotype A. arnoldi. Aldabrachelys hololissa was apparently extirpated from the wild in the 1800s and is now known only from 37 adults, including 28 captive, 1 free-ranging on Cerf Island, and 8 on Cousine Island, 6 of which were released in 2011 along with 40 captive bred juveniles. Captive reared juveniles show that there is a presumed genetic basis to the morphotype and further genetic work is needed to elucidate this. -
Download Vol. 20, No. 2
BULLETIN of the FLORIDA STATE MUSEUM Biological Sciences Volume 20 1976 Number 2 THE GENUS GOPHERUS ( TESTUDINIDAE ): PT. I. OSTEOLOGY AND RELATIONSHIPS OF EXTANT SPECIES WALTER AUFFENBERC e = UNIVERSITY OF FLORIDA GAINESVILLE Numbers of the BULLETIN OF THE FLORIDA STATE MUSEUM, BIOLOGICAL SCIENCES, are published at irregular intervals. Volumes contain about 300 pages and are not necessaril; completed in any one calendar year. CARTER R. GILBERT, Editor RHODA J, RYBAK, Managing Editor Consultants for this issue: JAMES L. DOBIE J, ALAN HOLMAN SAM R. TELFORD, JR. Communications concerning purchase or exchange of the publications and all man- uscripts should be addressed to the Managing Editor of the Bulletin, Florida State Museum, Museum Road, University of Florida, Gainesville, Florida 32611. This public document was promulgated at an annual cost of $2,561.67 or $2.328 per copy. It makes available to libraries, scholars, and all interested persons the results of researches in the natural sciences, emphasizing the Circum-Caribbean region. Publication date: January 23, 1976 Price $2.35 THE GENUS GOPHERUS (TESTUDINIDAE): PT. I. OSTEOLOGY AND RELATIONSHIPS OF EXTANT SPECIES WALTER AUFFENBERGl SYNOPSIS: Adult skeletons of the extant species of the genus Gopherus were studied to determine the kind and level of similarities and differences between them and to form a comparative base for studies of fossil members of the genus. The skeleton and its variation in each of the species is described and/or figured and analyzed. The four extant species form two species groups, based on a number of osteological characters. One group includes G. polyphemus and G, #avomarginatus, the other G. -
Cytogenetics and Morphology of Two Tortoise Species of the Genus Chelonoidis (Fitzinger, 1835) (Testudines)
Thesis Abstract Cytogenetics and morphology of two tortoise species of the genus Chelonoidis (Fitzinger, 1835) (Testudines) T.L. Silva 2011. Universidade Estadual Paulista “Júlio de Mesquita Filho”, São José do Rio Preto, SP, Brasil. MSc. thesis. Orienting Prof.: Maria Tercília Vilela de Azeredo Oliveira. Co-orienting Prof.: Claudia Regina Bonini Domingos. DOI 10.4238/vol10-2ta034 The reptiles were reduced in number of species since the time that they ruled the earth until today. The tortoises have been poorly studied, particularly their morphological and cytoge- netic features. We examined the species Chelonoidis carbonaria and C. denticulata, terrestrial tortoises representative of two contrasting biomes (Cerrado and Amazonia), to check for the existence of a possible C. carbonaria morphotype, and describe their karyotypes. The animals were collected from the “Reginaldo Uvo Leone” breeding farm, located in Tabapuã, SP. We made measurements of external morphology, in order to evaluate the morphological character- istics that could effectively allow differentiation of these two species of Brazilian tortoises, also examining a C. carbonaria morphotype that differs in color and size patterns established for this species. This C. carbonaria morphotype showed morphological characteristics intermediate be- tween these two species described. Cytogenetic studies gave a chromosome number of 2n = 52 for all three groups. G-banding did not give good reproducibility and consistency in the banding patterns. In C. carbonaria males, C-banding technique revealed constitutive heterochromatin in two microchromosomes and in two centromeric regions of macrochromosomes; in females only two microchromosomes showed specific staining. The species C. denticulata and the C. carbonaria morphotype did not have evident heterochromatic blocks. -
Giant Tortoises with Pinta Island Ancestry Identified In
Biological Conservation 157 (2013) 225–228 Contents lists available at SciVerse ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Short communication The genetic legacy of Lonesome George survives: Giant tortoises with Pinta Island ancestry identified in Galápagos a, a a,b c d Danielle L. Edwards ⇑, Edgar Benavides , Ryan C. Garrick , James P. Gibbs , Michael A. Russello , Kirstin B. Dion a, Chaz Hyseni a, Joseph P. Flanagan e, Washington Tapia f, Adalgisa Caccone a a Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520, USA b Department of Biology, University of Mississippi, MS 38677, USA c College of Environmental Science and Forestry, State University of New York, Syracuse, NY 13210, USA d Department of Biology, University of British Columbia, Okanagan Campus, Kelowna, BC, Canada V1V 1V7 e Houston Zoo, Houston, TX 77030, USA f Galápagos National Park Service, Puerto Ayora, Galápagos, Ecuador article info abstract Article history: The death of Lonesome George, the last known purebred individual of Chelonoidis abingdoni native to Received 22 August 2012 Pinta Island, marked the extinction of one of 10 surviving giant tortoise species from the Galápagos Archi- Received in revised form 9 October 2012 pelago. Using a DNA reference dataset including historical C. abingdoni and >1600 living Volcano Wolf Accepted 14 October 2012 tortoise samples, a site on Isabela Island known to harbor hybrid tortoises, we discovered 17 individuals with ancestry in C. abingdoni. These animals belong to various hybrid categories, including possible first generation hybrids, and represent multiple, unrelated individuals. Their ages and relative abundance sug- Keywords: gest that additional hybrids and conceivably purebred C. -
Growing and Shrinking in the Smallest Tortoise, Homopus Signatus Signatus: the Importance of Rain
CORE Metadata, citation and similar papers at core.ac.uk Provided by Springer - Publisher Connector Oecologia (2007) 153:479–488 DOI 10.1007/s00442-007-0738-7 GLOBAL CHANGE AND CONSERVATION ECOLOGY Growing and shrinking in the smallest tortoise, Homopus signatus signatus: the importance of rain Victor J. T. Loehr · Margaretha D. Hofmeyr · Brian T. Henen Received: 21 November 2006 / Accepted: 21 March 2007 / Published online: 24 April 2007 © Springer-Verlag 2007 Abstract Climate change models predict that the range of dorso-ventrally, so a reduction in internal matter due to the world’s smallest tortoise, Homopus signatus signatus, starvation or dehydration may have caused SH to shrink. will aridify and contract in the next decades. To evaluate Because the length and width of the shell seem more rigid, the eVects of annual variation in rainfall on the growth of reversible bone resorption may have contributed to shrink- H. s. signatus, we recorded annual growth rates of wild age, particularly of the shell width and plastron length. individuals from spring 2000 to spring 2004. Juveniles Based on growth rates for all years, female H. s. signatus grew faster than did adults, and females grew faster than need 11–12 years to mature, approximately twice as long as did males. Growth correlated strongly with the amount of would be expected allometrically for such a small species. rain that fell during the time just before and within the However, if aridiWcation lowers average growth rates to the growth periods. Growth rates were lowest in 2002–2003, level of 2002–2003, females would require 30 years to when almost no rain fell between September 2002 and mature.