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BIAWAK Quarterly Journal of Varanid Biology and Husbandry
BIAWAK Quarterly Journal of Varanid Biology and Husbandry Volume 4 Number 2 ISSN: 1936-296X On the Cover: Varanus obor Varanus obor is the most recent species of monitor lizard to be described from Indonesia. Discovered by Weijola and Sweet (2010. A new melanistic species of monitor [Reptilia: Squa- mata: Varanidae] from Sanana Island, Indone- sia. Zootaxa 2434: 17-32.), V. obor also repre- sents the most recently described member of the V. indicus complex. Data and observations on its natural history and ecology are included within the species description. The specimens depicted on the cover and inset of this issue were photographed by Valter Wei- jola on Sanana Island, Maluku, Indonesia on 28 March and 3 April 2009. The specimen depicted on the cover and to the left was observed around 1600 h in a coastal Sago area of northeastern Sanana. The specimen depicted below was first observed foraging in coastal vegetation, but as- cended a coconut palm when it noticed the ob- server. BIAWAK Quarterly Journal of Varanid Biology and Husbandry Editor Editorial Review ROBERT W. MENDYK MICHAEL J. BALSAI Center for Science Teaching and Learning Department of Biology, Temple University 1 Tanglewood Road Philadelphia, PA 19122, US Rockville Centre, NY 11570, US [email protected] [email protected] BERND EIDENMÜLLER Griesheimer Ufer 53 Associate Editors 65933 Frankfurt, DE [email protected] DANIEL BENNETT School of Biology, Leeds University MICHAEL FOST Leeds LS2 9JT, UK Department of Math and Statistics [email protected] Georgia State University Atlanta, GA 30303, US MICHAEL Cota [email protected] Thailand Natural History Museum, National Science Museum, RUston W. -
Why Do Most Tropical Animals Reproduce Seasonally? Testing Hypotheses on an Australian Snake
Ecology, 87(1), 2006, pp. 133±143 q 2006 by the Ecological Society of America WHY DO MOST TROPICAL ANIMALS REPRODUCE SEASONALLY? TESTING HYPOTHESES ON AN AUSTRALIAN SNAKE G. P. BROWN AND R. SHINE1 Biological Sciences A08, University of Sydney, New South Wales 2006 Australia Abstract. Most species reproduce seasonally, even in the tropics where activity occurs year-round. Squamate reptiles provide ideal model organisms to clarify the ultimate (adap- tive) reasons for the restriction of reproduction to speci®c times of year. Females of almost all temperate-zone reptile species produce their eggs or offspring in the warmest time of the year, thereby synchronizing embryogenesis with high ambient temperatures. However, although tropical reptiles are freed from this thermal constraint, most do not reproduce year-round. Seasonal reproduction in tropical reptiles might be driven by biotic factors (e.g., peak periods of predation on eggs or hatchlings, or food for hatchlings) or abiotic factors (e.g., seasonal availability of suitably moist incubation conditions). Keelback snakes (Tropidonophis mairii, Colubridae) in tropical Australia reproduce from April to November, but with a major peak in May±June. Our ®eld studies falsify hypotheses that invoke biotic factors as explanations for this pattern: the timing of nesting does not minimize predation on eggs, nor maximize food availability or survival rates for hatchlings. Instead, our data implicate abiotic factors: female keelbacks nest most intensely soon after the cessation of monsoonal rains when soils are moist enough to sustain optimal embryogenesis (wetter nests produce larger hatchlings, that are more likely to survive) but are unlikely to become waterlogged (which is lethal to eggs). -
Life History of the Coppertail Skink (Ctenotus Taeniolatus) in Southeastern Australia
Herpetological Conservation and Biology 15(2):409–415. Submitted: 11 February 2020; Accepted: 19 May 2020; Published: 31 August 2020. LIFE HISTORY OF THE COPPERTAIL SKINK (CTENOTUS TAENIOLATUS) IN SOUTHEASTERN AUSTRALIA DAVID A. PIKE1,2,6, ELIZABETH A. ROZNIK3, JONATHAN K. WEBB4, AND RICHARD SHINE1,5 1School of Biological Sciences A08, University of Sydney, New South Wales 2006, Australia 2Present address: Department of Biology, Rhodes College, Memphis, Tennessee 38112, USA 3Department of Conservation and Research, Memphis Zoo, Memphis, Tennessee 38112, USA 4School of Life Sciences, University of Technology Sydney, Broadway, New South Wales 2007, Australia 5Present address: Department of Biological Sciences, Macquarie University, New South Wales 2109, Australia 6Corresponding author, e-mail: [email protected] Abstract.—The global decline of reptiles is a serious problem, but we still know little about the life histories of most species, making it difficult to predict which species are most vulnerable to environmental change and why they may be vulnerable. Life history can help dictate resilience in the face of decline, and therefore understanding attributes such as sexual size dimorphism, site fidelity, and survival rates are essential. Australia is well-known for its diversity of scincid lizards, but we have little detailed knowledge of the life histories of individual scincid species. To examine the life history of the Coppertail Skink (Ctenotus taeniolatus), which uses scattered surface rocks as shelter, we estimated survival rates, growth rates, and age at maturity during a three-year capture-mark- recapture study. We captured mostly females (> 84%), and of individuals captured more than once, we captured 54.3% at least twice beneath the same rock, and of those, 64% were always beneath the same rock (up to five captures). -
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. -
Maternal Nest-Site Choice and Offspring Fitness in a Tropical Snake (Tropidonophis Mairii, Colubridae)
Ecology, 85(6), 2004, pp. 1627±1634 q 2004 by the Ecological Society of America MATERNAL NEST-SITE CHOICE AND OFFSPRING FITNESS IN A TROPICAL SNAKE (TROPIDONOPHIS MAIRII, COLUBRIDAE) G. P. BROWN AND R. SHINE1 Biological Sciences A08, University of Sydney, NSW 2006 Australia Abstract. Do reproducing female reptiles adaptively manipulate phenotypic traits of their offspring by selecting appropriate nest sites? Evidence to support this hypothesis is indirect, mostly involving the distinctive characteristics of used (vs. available) nest sites, and the fact that physical conditions during egg incubation can modify hatchling phenotypic traits that plausibly might in¯uence ®tness. Such data fall well short of demonstrating that nesting females actively select from among potential sites based on cues that predict ®tness- determining phenotypic modi®cations of their offspring. We provide such data from ex- perimental studies on a small oviparous snake (the keelback, Tropidonophis mairii) from the wet-dry tropics of Australia. When presented with a choice of alternative nesting sites, egg-laying females selected more moist substrates for egg deposition. Incubation on wetter substrates signi®cantly increased body size at hatching, a trait under strong positive selection in this population (based on mark±recapture studies of free-ranging hatchlings). Remark- ably, the hydric conditions experienced by an egg in the ®rst few hours after it was laid substantially affected phenotypic traits (notably, muscular strength) of the hatchling that emerged from that egg 10 weeks later. Thus, our data provide empirical support for the hypothesis that nesting female reptiles manipulate the phenotypic traits of their offspring through nest-site selection, in ways that enhance offspring ®tness. -
Draft Animal Keepers Species List
Revised NSW Native Animal Keepers’ Species List Draft © 2017 State of NSW and Office of Environment and Heritage With the exception of photographs, the State of NSW and Office of Environment and Heritage are pleased to allow this material to be reproduced in whole or in part for educational and non-commercial use, provided the meaning is unchanged and its source, publisher and authorship are acknowledged. Specific permission is required for the reproduction of photographs. The Office of Environment and Heritage (OEH) has compiled this report in good faith, exercising all due care and attention. No representation is made about the accuracy, completeness or suitability of the information in this publication for any particular purpose. OEH shall not be liable for any damage which may occur to any person or organisation taking action or not on the basis of this publication. Readers should seek appropriate advice when applying the information to their specific needs. All content in this publication is owned by OEH and is protected by Crown Copyright, unless credited otherwise. It is licensed under the Creative Commons Attribution 4.0 International (CC BY 4.0), subject to the exemptions contained in the licence. The legal code for the licence is available at Creative Commons. OEH asserts the right to be attributed as author of the original material in the following manner: © State of New South Wales and Office of Environment and Heritage 2017. Published by: Office of Environment and Heritage 59 Goulburn Street, Sydney NSW 2000 PO Box A290, -
Antibacterial Activities of Serum from the Komodo Dragon (Varanus
Microbiology Research 2013; volume 4:e4 Antibacterial activities Introduction Correspondence: Mark Merchant, DEof Bioche - of serum from the Komodo mistry, McNeese State University Dragon (Varanus komodoensis) The Komodo dragon (Varanus komodoensis) Lake Charles, LA 70609, USA. Tel. +1.337.4755773 is an endangered species of monitor lizard E-mail: [email protected] Mark Merchant,1 Danyell Henry,1 indigenous to only five islands in the Lesser Key words: innate immunity, lizard, reptile, Rodolfo Falconi,1 Becky Muscher,2 Sunda region of southeast Indonesia.1 It is the serum complement, varanid. Judith Bryja3 largest lizard in the world, reaching lengths of 2 1Department of Chemistry, McNeese more than 3 meters. These reptiles primarily Acknowledgements: the authors wish to acknowl- State University, Lake Charles, LA; inhabit the tropical savannahs, and their edge the help of San Antonio Zoo employees: J. 2Department of Herpetology, San boundary woodlands, of these islands. They Stephen McCusker (Director), Alan Kardon 3 (Curator of Herpetology and Aquarium), and Rob Antonio Zoo, TX; 3Department of feed as both scavenger and predators, eating a broad spectrum of food items. Coke and Jenny Nollman (Veterinarians), and Herpetology, Houston Zoo, TX, USA Komodo dragons kill prey items with a lethal Houston Zoo employees Rick Barongi (Director), bite that is believed to inject toxic bacteria into Stan Mays (Director of Herpetology), and Maryanne Tocidlowski (Veterinarian), for per- the blood stream of these animals.4-5 However, mission to -
E-Program DO NOT PRINT!
e-program DO NOT PRINT! You’ll receive a pocket program at registration, so no need to print this one. This e-program includes all presentation sessions and the associated abstracts, which are hyperlinked to the name of the presenter. Plenary abstracts are included in the pocket program. The plan on a page Tuesday June 20 Wednesday June 21 Thursday June 22 Friday June 23 7:30-8:30 am Breakfast: 7:30-8:30am Breakfast: 7:30-8:30am Breakfast: Dining Hall Dining Hall Dining Hall 8:50-10:00am Plenary: 8:50-10:00am Plenary: 8:50-10:00am Plenary: Rick Sabrina Fossette-Halot - Renee Catullo - Chapel. Shine - Chapel. Introduced Chapel. Introduced by Nicki Introduced by Scott Keogh by Ben Philips Mitchell 10:00-10:25 am Tea break 10:00-10:15am Tea break 10:00-10:25am Tea break 10:30-11:54am Short 10:20am -12:00pm Mike Bull 10:30-11:42am Short Talks: Talks: Session 1 - Symposium - Chapel Session 8 - Clubhouse: Clubhouse: upstairs and upstairs and downstairs downstairs 11:45 Conference close (upstairs) 12:00-2:00pm Lunch 12:00-1:00pm Conference 12:00-1:00pm Lunch: Dining (Dining Hall) and ASH photo and lunch Hall or Grab and Go, buses AGM (Clubhouse upstairs) depart for airport from midday High ropes course and 1:00-2:00pm Short Talks: climbing wall open. Book at Session 5 - Clubhouse: registration on Tuesday if upstairs and downstairs interested 2:00 -4:00pm 2:00-3:00pm Speed talks: 2:00-3:00pm Speed talks: Registration, locate Session 2 Clubhouse Session 6 Clubhouse accommodation, light upstairs upstairs fires, load talks, book activities 3:00-3:25pm -
Reptiles of the Wet Tropics
Reptiles of the Wet Tropics The concentration of endemic reptiles in the Wet Tropics is greater than in any other area of Australia. About 162 species of reptiles live in this region and 24 of these species live exclusively in the rainforest. Eighteen of them are found nowhere else in the world. Many lizards are closely related to species in New Guinea and South-East Asia. The ancestors of two of the resident geckos are thought to date back millions of years to the ancient super continent of Gondwana. PRICKLY FOREST SKINK - Gnypetoscincus queenlandiae Length to 17cm. This skink is distinguished by its very prickly back scales. It is very hard to see, as it is nocturnal and hides under rotting logs and is extremely heat sensitive. Located in the rainforest in the Wet Tropics only, from near Cooktown to west of Cardwell. RAINFOREST SKINK - Eulamprus tigrinus Length to 16cm. The body has irregular, broken black bars. They give birth to live young and feed on invertebrates. Predominantly arboreal, they bask in patches of sunlight in the rainforest and shelter in tree hollows at night. Apparently capable of producing a sharp squeak when handled or when fighting. It is rare and found only in rainforests from south of Cooktown to west of Cardwell. NORTHERN RED-THROATED SKINK - Carlia rubrigularis Length to 14cm. The sides of the neck are richly flushed with red in breeding males. Lays 1-2 eggs per clutch, sometimes communally. Forages for insects in leaf litter, fallen logs and tree buttresses. May also prey on small skinks and own species. -
Iguanid and Varanid CAMP 1992.Pdf
CONSERVATION ASSESSMENT AND MANAGEMENT PLAN FOR IGUANIDAE AND VARANIDAE WORKING DOCUMENT December 1994 Report from the workshop held 1-3 September 1992 Edited by Rick Hudson, Allison Alberts, Susie Ellis, Onnie Byers Compiled by the Workshop Participants A Collaborative Workshop AZA Lizard Taxon Advisory Group IUCN/SSC Conservation Breeding Specialist Group SPECIES SURVIVAL COMMISSION A Publication of the IUCN/SSC Conservation Breeding Specialist Group 12101 Johnny Cake Ridge Road, Apple Valley, MN 55124 USA A contribution of the IUCN/SSC Conservation Breeding Specialist Group, and the AZA Lizard Taxon Advisory Group. Cover Photo: Provided by Steve Reichling Hudson, R. A. Alberts, S. Ellis, 0. Byers. 1994. Conservation Assessment and Management Plan for lguanidae and Varanidae. IUCN/SSC Conservation Breeding Specialist Group: Apple Valley, MN. Additional copies of this publication can be ordered through the IUCN/SSC Conservation Breeding Specialist Group, 12101 Johnny Cake Ridge Road, Apple Valley, MN 55124. Send checks for US $35.00 (for printing and shipping costs) payable to CBSG; checks must be drawn on a US Banlc Funds may be wired to First Bank NA ABA No. 091000022, for credit to CBSG Account No. 1100 1210 1736. The work of the Conservation Breeding Specialist Group is made possible by generous contributions from the following members of the CBSG Institutional Conservation Council Conservators ($10,000 and above) Australasian Species Management Program Gladys Porter Zoo Arizona-Sonora Desert Museum Sponsors ($50-$249) Chicago Zoological -
Qryholdings Scientific Name Species Code Common Name Number of Licensees Acquired Bred Disposed Hoplocephalus Bitorquatus W2675
qryHoldings Number of Scientific_Name Species_Code Common_Name Acquired Bred Disposed licensees Hoplocephalus bitorquatus W2675 Pale-headed Snake 14 7 314 Hoplocephalus bitorquatus x H. stephensii X2001 Pale-headed X Stephen's Banded Snake hybrid 1 Hoplocephalus bungaroides A2676 Broad-headed Snake 7 4 0 6 Hoplocephalus stephensii C2677 Stephens' Banded Snake 21 9 9 21 Pseudechis colletti W2691 Collett’s Snake 41 18 18 Pseudechis porphyriacus C2693 Red-bellied Black Snake 80 39 55 66 Vermicella annulata M2734 Eastern Bandy-bandy 2 3 Acanthophis antarcticus A2640 Southern Death Adder 59 76 105 95 Acanthophis praelongus Y2804 Northern Death Adder 24 41 0 23 Acanthophis pyrrhus C2641 Desert Death Adder 8 1 0 6 Austrelaps ramsayi W2615 Highlands Copperhead 20 3 0 26 Austrelaps superbus E2642 Lowlands Copperhead 12 14 0 25 Notechis ater Q2680 Black Tiger Snake 8 9 0 9 Notechis scutatus S2681 Common Tiger Snake 45 40 23 55 Pseudechis australis U2690 Mulga Snake 31 23 19 29 Pseudechis butleri M2814 Butler's Snake 1 1 Pseudechis guttatus A2692 Spotted Black Snake 20 12 5 16 Pseudonaja guttata G2695 Speckled Brown Snake 2 4 4 Pseudonaja modesta K2697 Ringed Brown Snake 1 Pseudonaja nuchalis M2698 Western Brown Snake 4 5 2 Rhinoplocephalus nigrescens E2650 EasternSmall-eyed Snake 3 6 Oxyuranus microlepidotus K2689 Western Taipan 25 10 12 21 Oxyuranus scutellatus Y2688 Taipan 17 20 24 45 Pseudonaja textilis Z2699 Common Brown Snake 32 28 35 41 Tropidechis carinatus G2723 Rough-scaled Snake 12 10 11 16 Crocodylus johnstoni K2001 Freshwater Crocodile -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica.