Suggested Guidelines for Reptiles and Amphibians Used in Outreach
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Cyclura Or Rock Iguanas Cyclura Spp
Cyclura or Rock Iguanas Cyclura spp. There are 8 species and 16 subspecies of Cyclura that are thought to exist today. All Cyclura species are endangered and are listed as CITES (Convention on International Trade in Endangered Species) Appendix I, the highest level of pro- tection the Convention gives. Wild Cyclura are only found in the Caribbean, with many subspecies endemic to only one particular island in the West Indies. Cyclura mature and grow slowly compared to other lizards in the family Iguani- dae, and have a very long life span (sometimes reaches ages of 50+ years). The more common species in the pet trade in- clude the Rhinoceros Iguana (Cyclura cornuta cornuta), and Cuban Rock Iguana (juvenile), the Cuban Rock Iguana (Cyclura nubila nubila). Cyclura nubila nubila Basic Care: Habitat: Cyclura care is similar to that of the Green Iguana (Iguana iguana), but there are some major differences. Cyclura Iguanas are generally ground-dwelling lizards, and require a very large cage with lots of floor space. The suggested minimum space to keep one or two adult Cyclura in captivity is usually a cage that is at the very least 10’X10’. Because of this space requirement, many cyclura owners choose to simply des- ignate a room of their home to free-roaming. If a male/female pair are to be kept to- gether, multiple basking spots, feeding stations, and hides will be required. All Cyclura are extremely territorial and can inflict serious injuries or even death to their cage- mates unless monitored carefully. The recommended temperature for Cyclura is a basking spot of about 95-100F during the day, with a temperature gradient of cooler areas to escape the heat. -
(EU) 2015/56 Оd 15
16.1.2015. HR Službeni list Europske unije L 10/1 II. (Nezakonodavni akti) UREDBE UREDBA KOMISIJE (EU) 2015/56 оd 15. siječnja 2015. o izmjeni, u odnosu na trgovinu vrstama divlje faune i flore, Uredbe (EZ) br. 865/2006 o utvrđivanju detaljnih pravila o provedbi Uredbe Vijeća (EZ) br. 338/97 EUROPSKA KOMISIJA, uzimajući u obzir Ugovor o funkcioniranju Europske unije, uzimajući u obzir Uredbu Vijeća (EZ) br. 338/97 od 9. prosinca 1996. o zaštiti vrsta divlje faune i flore uređenjem trgovine njima (1), a posebno njezin članak 19. stavke 2., 3. i 4., budući da: (1) Za provedbu određenih rezolucija donesenih na šesnaestom sastanku Konferencije potpisnica Konvencije o međunarodnoj trgovini ugroženim vrstama divlje faune i flore (CITES) (3. – 14. ožujka 2013.), u daljnjem tekstu „Konvencija”, neke odredbe treba izmijeniti, a daljnje odredbe treba dodati Uredbi Komisije (EZ) br. 865/2006 (2). (2) Posebno, u skladu s Rezolucijom Konferencije potpisnica CITES-a 16.8, treba umetnuti posebne odredbe namijenjene pojednostavljenju nekomercijalnog prekograničnog prometa glazbenih instrumenata. (3) Iskustvo stečeno provedbom Uredbe (EZ) br. 865/2006, u vezi s Provedbenom uredbom Komisije (EU) br. 792/2012 (3), pokazalo je da neke njezine odredbe treba izmijeniti kako bi se osigurala usklađena i učinkovita provedba Uredbe unutar Unije. To je posebno slučaj kod prvog unošenja u Uniju lovačkih trofeja primjeraka nekih vrsta ili populacija navedenih u Prilogu B Uredbi (EZ) br. 338/97, za koje postoji zabrinutost u pogledu održivosti trgovine lovačkim trofejima ili za koje postoje naznake značajne nezakonite trgovine. U takvim je slučajevima potreban stroži nadzor uvoza u Uniju, a odstupanje utvrđeno člankom 7. -
HERPETOLOGICAL BULLETIN Number 106 – Winter 2008
The HERPETOLOGICAL BULLETIN Number 106 – Winter 2008 PUBLISHED BY THE BRITISH HERPETOLOGICAL SOCIETY THE HERPETOLOGICAL BULLETIN Contents RESEA R CH AR TICLES Use of transponders in the post-release monitoring of translocated spiny-tailed lizards (Uromastyx aegyptia microlepis) in Abu Dhabi Emirate, United Arab Emirates Pritpal S. Soorae, Judith Howlett and Jamie Samour .......................... 1 Gastrointestinal helminths of three species of Dicrodon (Squamata: Teiidae) from Peru Stephen R. Goldberg and Charles R. Bursey ..................................... 4 Notes on the Natural History of the eublepharid Gecko Hemitheconyx caudicinctus in northwestern Ghana Stephen Spawls ........................................................ 7 Significant range extension for the Central American Colubrid snake Ninia pavimentata (Bocourt 1883) Josiah H. Townsend, J. Micheal Butler, Larry David Wilson, Lorraine P. Ketzler, John Slapcinsky and Nathaniel M. Stewart ..................................... 15 Predation on Italian Newt larva, Lissotriton italicus (Amphibia, Caudata, Salamandridae), by Agabus bipustulatus (Insecta, Coleoptera, Dytiscidae) Luigi Corsetti and Gianluca Nardi........................................ 18 Behaviour, Time Management, and Foraging Modes of a West Indian Racer, Alsophis sibonius Lauren A. White, Peter J. Muelleman, Robert W. Henderson and Robert Powell . 20 Communal egg-laying and nest-sites of the Goo-Eater, Sibynomorphus mikanii (Colubridae, Dipsadinae) in southeastern Brazil Henrique B. P. Braz, Francisco L. Franco -
West Indian Iguana Husbandry Manual
1 Table of Contents Introduction ................................................................................................................................... 4 Natural history ............................................................................................................................... 7 Captive management ................................................................................................................... 25 Population management .............................................................................................................. 25 Quarantine ............................................................................................................................... 26 Housing..................................................................................................................................... 26 Proper animal capture, restraint, and handling ...................................................................... 32 Reproduction and nesting ........................................................................................................ 34 Hatchling care .......................................................................................................................... 40 Record keeping ........................................................................................................................ 42 Husbandry protocol for the Lesser Antillean iguana (Iguana delicatissima)................................. 43 Nutrition ...................................................................................................................................... -
How to Tell the Difference Between Native Rock Iguanas and Invasive Green Iguanas by Elaine A
How to Tell the Difference Between Native Rock Iguanas and Invasive Green Iguanas By Elaine A. Powers Illustrated by Anderson Atlas Many of the islands in the Caribbean Sea, known as the West Rock Iguanas (Cyclura) Indies, have native iguanas. B Cuban Rock Iguana (Cyclura nubila), Cuba They are called Rock Iguanas. C Sister Isles Rock Iguana (Cyclura nubila caymanensis), Cayman Brac and Invasive Green Iguanas have been introduced on these islands and Little Cayman are a threat to the Rock Iguanas. They compete for food, territory D Grand Cayman Blue Iguana (Cyclura lewisi), Grand Cayman and nesting areas. E Jamaican Rock Iguana (Cyclura collei), Jamaica This booklet is designed to help you identify the native Rock F Turks & Caicos Rock Iguana (Cyclura carinata), Turks and Caicos. Iguanas from the invasive Greens. G Booby Cay Rock Iguana (Cyclura carinata bartschi), Booby Cay, Bahamas H Andros Rock Iguana (Cyclura cychlura), Andros, Bahamas West Indies I Exuma Rock Iguana (Cyclura cychlura figginsi), Exuma Islands, Bahamas Exumas BAHAMAS J Allen’s Cay Rock Iguana (Cyclura cychlura inornata), Exuma Islands, J Islands Bahamas M San Salvador Andros Island H Booby Cay K Anegada Iguana (Cyclura pinguis), British Virgin Islands Allens Cay White G I Cay Ricord’s Iguana (Cyclura ricordi), Hispaniola O F Turks & Caicos L CUBA NAcklins Island M San Salvador Rock Iguana (Cyclura rileyi), San Salvador, Bahamas Anegada HISPANIOLA CAYMAN ISLANDS K N Acklins Rock Iguana (Cyclura rileyi nuchalis), Acklins Islands, Bahamas B PUERTO RICO O White Cay Rock Iguana (Cyclura rileyi cristata), Exuma Islands, Bahamas Grand Cayman D C JAMAICA BRITISH P Rhinoceros Iguana (Cyclura cornuta), Hispanola Cayman Brac & VIRGIN Little Cayman E L P Q Mona ISLANDS Q Mona Island Iguana (Cyclura stegnegeri), Mona Island, Puerto Rico Island 2 3 When you see an iguana, ask: What kind do I see? Do you see a big face scale, as round as can be? What species is that iguana in front of me? It’s below the ear, that’s where it will be. -
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Vol. 78: 87–95, 2007 DISEASES OF AQUATIC ORGANISMS Published December 13 doi: 10.3354/dao01861 Dis Aquat Org Survey for the amphibian chytrid Batrachochytrium dendrobatidis in Hong Kong in native amphibians and in the international amphibian trade Jodi J. L. Rowley1, 5,*, Simon Kin Fung Chan2, Wing Sze Tang2, Richard Speare3, Lee F. Skerratt 4, Ross A. Alford1, Ka Shing Cheung 2, Ching Yee Ho2, Ruth Campbell4 1School of Marine and Tropical Biology and Amphibian Disease Ecology Group, James Cook University, Townsville, Queensland, Australia 4811 2Herpetofauna Working Group, Agriculture, Fisheries and Conservation Department, The Government of the Hong Kong Special Administrative Region, 7/F, Cheung Sha Wan Government Offices, 303 Cheung Sha Wan Road, Kowloon, Hong Kong, China 3School of Public Health, Tropical Medicine and Rehabilitation and Amphibian Disease Ecology Group, James Cook University, Townsville, Queensland, Australia 4811 4School of Veterinary and Biomedical Sciences and Amphibian Disease Ecology Group, James Cook University, Townsville, Queensland, Australia 4811 5Present address: Conservation International Indo-Burma, PO Box 1356, Phnom Penh, Cambodia ABSTRACT: Chytridiomycosis, caused by the pathogen Batrachochytrium dendrobatidis, is respon- sible for many amphibian declines and has been identified in wild amphibian populations on all con- tinents where they exist, except for Asia. In order to assess whether B. dendrobatidis is present on the native amphibians of Hong Kong, we sampled wild populations of Amolops hongkongensis, Paa exil- ispinosa, P. spinosa and Rana chloronota during 2005–2006. Amphibians infected with B. dendro- batidis have been found in the international trade, so we also examined the extent and nature of the amphibian trade in Hong Kong during 2005–2006, and assessed whether B. -
Analyses of Proposals to Amend
CoP17 Prop. 38 Inclusion of False Tomato Frog Dyscophus guineti and Antsouhy Tomato Frog D. insularis in Appendix II Proponent: Madagascar Summary: The False Tomato Frog Dyscophus guineti and the Antsouhy Tomato Frog D. insularis comprise two of three species in the genus Dyscophus, all of which are endemic to Madagascar. The third species, D. antongilii was included in Appendix I in 1987. It is subject to a separate proposal to be transferred from Appendix I to Appendix II (Proposal 37). All three are attractive red-orange coloured frogs. Dyscophus are known to breed explosively with the availability of water during the rainy season (typically January-March) and during that time they can be found in abundance at breeding sites. Hundreds of eggs are laid in water following mating. Dyscophus guineti The known distribution of D. guineti includes a number of patches in the remnant central eastern rainforest of Madagascar. The species is secretive and believed likely to be more widespread than records indicate1. Overall population is unknown; locally the species can vary from extremely common to very rare1. Sexual maturity is attained between two and four years, comparatively earlier in males than in females2. The habitat of the species is affected by conversion of forest to agriculture, timber extraction, charcoal production and potentially small-scale mining activities. The species reportedly does not tolerate severe degredation1. There is not known to be local use of the species. As a consequence of the Appendix-I listing in 1987 of the similar Dyscophus antongilii, collectors interested in "red Dyscophus" have shifted their attention to D. -
Aberrant Colourations in Wild Snakes: Case Study in Neotropical Taxa and a Review of Terminology
SALAMANDRA 57(1): 124–138 Claudio Borteiro et al. SALAMANDRA 15 February 2021 ISSN 0036–3375 German Journal of Herpetology Aberrant colourations in wild snakes: case study in Neotropical taxa and a review of terminology Claudio Borteiro1, Arthur Diesel Abegg2,3, Fabrício Hirouki Oda4, Darío Cardozo5, Francisco Kolenc1, Ignacio Etchandy6, Irasema Bisaiz6, Carlos Prigioni1 & Diego Baldo5 1) Sección Herpetología, Museo Nacional de Historia Natural, Miguelete 1825, Montevideo 11800, Uruguay 2) Instituto Butantan, Laboratório Especial de Coleções Zoológicas, Avenida Vital Brasil, 1500, Butantã, CEP 05503-900 São Paulo, SP, Brazil 3) Universidade de São Paulo, Instituto de Biociências, Departamento de Zoologia, Programa de Pós-Graduação em Zoologia, Travessa 14, Rua do Matão, 321, Cidade Universitária, 05508-090, São Paulo, SP, Brazil 4) Universidade Regional do Cariri, Departamento de Química Biológica, Programa de Pós-graduação em Bioprospecção Molecular, Rua Coronel Antônio Luiz 1161, Pimenta, Crato, Ceará 63105-000, CE, Brazil 5) Laboratorio de Genética Evolutiva, Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas Químicas y Naturales, Universidad Nacional de Misiones, Felix de Azara 1552, CP 3300, Posadas, Misiones, Argentina 6) Alternatus Uruguay, Ruta 37, km 1.4, Piriápolis, Uruguay Corresponding author: Claudio Borteiro, e-mail: [email protected] Manuscript received: 2 April 2020 Accepted: 18 August 2020 by Arne Schulze Abstract. The criteria used by previous authors to define colour aberrancies of snakes, particularly albinism, are varied and terms have widely been used ambiguously. The aim of this work was to review genetically based aberrant colour morphs of wild Neotropical snakes and associated terminology. We compiled a total of 115 cases of conspicuous defective expressions of pigmentations in snakes, including melanin (black/brown colour), xanthins (yellow), and erythrins (red), which in- volved 47 species of Aniliidae, Boidae, Colubridae, Elapidae, Leptotyphlopidae, Typhlopidae, and Viperidae. -
Leopard Geckos & African Fat-Tails Geckos
A Compassionate Commitment to Quality Pet Care! LEOPARD GECKOS & AFRICAN FAT-TAILS GECKOS SPECIES NAMES Leopard geckos (Eublepharis maclarius), African fat-tailed geckos (Hemitheconyx caudicinctus). Both are members of the Eublepharidae family, which includes all species of geckos with moveable eyelids. CAGING/HOUSING For a single gecko, a 10-gallon glass aquarium with a securely fastened wire mesh top is appropriate. For two or more geckos a 20- gallon or larger aquarium is necessary. For substrate use paper towels, newspaper, or artificial turf, washed orchard bark, or aquarium gravel. The use of sand or calcium-fortified sand (such as ReptiSand™ or Calci-Sand™) is not recommended for geckos less than 6 inches in length, due to the risk of ingestion and subsequent impaction in the gastrointestinal tract. A hide-box, or shelter, should be provided to allow the gecko a quiet retreat. LIGHTING/HEATING In order to properly thermo-regulate, leopard geckos need a temperature gradient that allows them to move from a cooler end of the tank to a warmer end. This temperature gradient should range between 70°F at the cool end at 85°F at the high end. African fat-tailed geckos require slightly higher temperatures ranging from between 80°F and 92°F. Since these geckos are nocturnal, UV lighting is not necessary. HUMIDITY A moderate level of humidity is required for these geckos, which can be provided by misting and providing a large water bowl for the animal to soak in. Low humidity levels can lead to problems with shedding. FEEDING Food items, as a general rule, should be no longer than the length, and less than half the width of the geckos head. -
Controlled Animals
Environment and Sustainable Resource Development Fish and Wildlife Policy Division Controlled Animals Wildlife Regulation, Schedule 5, Part 1-4: Controlled Animals Subject to the Wildlife Act, a person must not be in possession of a wildlife or controlled animal unless authorized by a permit to do so, the animal was lawfully acquired, was lawfully exported from a jurisdiction outside of Alberta and was lawfully imported into Alberta. NOTES: 1 Animals listed in this Schedule, as a general rule, are described in the left hand column by reference to common or descriptive names and in the right hand column by reference to scientific names. But, in the event of any conflict as to the kind of animals that are listed, a scientific name in the right hand column prevails over the corresponding common or descriptive name in the left hand column. 2 Also included in this Schedule is any animal that is the hybrid offspring resulting from the crossing, whether before or after the commencement of this Schedule, of 2 animals at least one of which is or was an animal of a kind that is a controlled animal by virtue of this Schedule. 3 This Schedule excludes all wildlife animals, and therefore if a wildlife animal would, but for this Note, be included in this Schedule, it is hereby excluded from being a controlled animal. Part 1 Mammals (Class Mammalia) 1. AMERICAN OPOSSUMS (Family Didelphidae) Virginia Opossum Didelphis virginiana 2. SHREWS (Family Soricidae) Long-tailed Shrews Genus Sorex Arboreal Brown-toothed Shrew Episoriculus macrurus North American Least Shrew Cryptotis parva Old World Water Shrews Genus Neomys Ussuri White-toothed Shrew Crocidura lasiura Greater White-toothed Shrew Crocidura russula Siberian Shrew Crocidura sibirica Piebald Shrew Diplomesodon pulchellum 3. -
Acrantophis Madagascariensis (Duméril & Bibron, 1844) and A
Kent Academic Repository Full text document (pdf) Citation for published version Gardner, Charlie J. and McDonnell, Naidi and Ellis, Charlotte and Jasper, Louise D. (2017) Observations of aquatic behaviour in Malagasy ground boas Acrantophis madagascariensis (Duméril & Bibron, 1844) and A. dumerili Jan, 1860. Herpetology Notes, 10 . pp. 271-273. DOI Link to record in KAR https://kar.kent.ac.uk/84414/ Document Version Author's Accepted Manuscript Copyright & reuse Content in the Kent Academic Repository is made available for research purposes. Unless otherwise stated all content is protected by copyright and in the absence of an open licence (eg Creative Commons), permissions for further reuse of content should be sought from the publisher, author or other copyright holder. Versions of research The version in the Kent Academic Repository may differ from the final published version. Users are advised to check http://kar.kent.ac.uk for the status of the paper. Users should always cite the published version of record. Enquiries For any further enquiries regarding the licence status of this document, please contact: [email protected] If you believe this document infringes copyright then please contact the KAR admin team with the take-down information provided at http://kar.kent.ac.uk/contact.html 1 Observations of aquatic behaviour in Malagasy ground boas 2 Acrantophis madagascariensis (Duméril & Bibron, 1844) and A. 3 dumerili Jan, 1860 4 5 Charlie J. GardnerI, Naidi McDonnellII, Charlotte EllisII and Louise D. JasperIII 6 7 8 I Durrell Institute of Conservation and Ecology, University of Kent, Canterbury, CT2 7NR, 9 UK 10 II Operation Wallacea, Wallace House, Old Bolingbroke, Spilsby, Lincolnshire, PE23 4EX, 11 UK 12 III Independent Researcher 13 14 Madagascar possesses a diverse snake fauna comprising over 90 species in four families 15 (Jenkins et al. -
Body-Size Effect on Egg Size in Eublepharid Geckos (Squamata
Blackwell Publishing LtdOxford, UKBIJBiological Journal of the Linnean Society0024-4066The Linnean Society of London, 20062006 884 527532 Original Article EGG-SIZE ALLOMETRY IN EUBLEPHARID GECKOS L. KRATOCHVÍL and D. FRYNTA Biological Journal of the Linnean Society, 2006, 88, 527–532. With 2 figures Body-size effect on egg size in eublepharid geckos (Squamata: Eublepharidae), lizards with invariant clutch size: negative allometry for egg size in ectotherms is not universal LUKÁT KRATOCHVÍL1* and DANIEL FRYNTA2 1Department of Ecology, Charles University, Vinidná 7, CZ-128 44 Praha 2, the Czech Republic 2Department of Zoology, Charles University, Vinidná 7, CZ-128 44 Praha 2, the Czech Republic Received 1 February 2005; accepted for publication 5 December 2005 Within a single clutch, smaller species of ectotherms generally lay a smaller number of relatively larger eggs than do larger species. Many hypotheses explaining both the interspecific negative allometry in egg size and egg size– number trade-off postulate the existence of an upper limit to the egg size of larger species. Specifically, in lizards, large eggs of large species could have too long a duration of incubation, or they could be too large to pass through the pelvic opening, which is presumably constrained mechanically in larger species. Alternatively, negative allometry could be a result of limits affecting eggs of smaller species. Under the latter concept, hatchling size in smaller species may be close to the lower limit imposed by ecological interactions or physiological processes, and therefore smaller species have to invest in relatively larger offspring. Contrary to these lower limit hypotheses, explanations based on the existence of an upper limit always predict negative egg-size allometry even in animals with invariant clutch size, in which naturally there is no egg size–number trade-off.