Chapter 2 Snakes of Papua New Guinea
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Neurotoxic Effects of Venoms from Seven Species of Australasian Black Snakes (Pseudechis): Efficacy of Black and Tiger Snake Antivenoms
Clinical and Experimental Pharmacology and Physiology (2005) 32, 7–12 NEUROTOXIC EFFECTS OF VENOMS FROM SEVEN SPECIES OF AUSTRALASIAN BLACK SNAKES (PSEUDECHIS): EFFICACY OF BLACK AND TIGER SNAKE ANTIVENOMS Sharmaine Ramasamy,* Bryan G Fry† and Wayne C Hodgson* *Monash Venom Group, Department of Pharmacology, Monash University, Clayton and †Australian Venom Research Unit, Department of Pharmacology, University of Melbourne, Parkville, Victoria, Australia SUMMARY the sole clad of venomous snakes capable of inflicting bites of medical importance in the region.1–3 The Pseudechis genus (black 1. Pseudechis species (black snakes) are among the most snakes) is one of the most widespread, occupying temperate, widespread venomous snakes in Australia. Despite this, very desert and tropical habitats and ranging in size from 1 to 3 m. little is known about the potency of their venoms or the efficacy Pseudechis australis is one of the largest venomous snakes found of the antivenoms used to treat systemic envenomation by these in Australia and is responsible for the vast majority of black snake snakes. The present study investigated the in vitro neurotoxicity envenomations. As such, the venom of P. australis has been the of venoms from seven Australasian Pseudechis species and most extensively studied and is used in the production of black determined the efficacy of black and tiger snake antivenoms snake antivenom. It has been documented that a number of other against this activity. Pseudechis from the Australasian region can cause lethal 2. All venoms (10 g/mL) significantly inhibited indirect envenomation.4 twitches of the chick biventer cervicis nerve–muscle prepar- The envenomation syndrome produced by Pseudechis species ation and responses to exogenous acetylcholine (ACh; varies across the genus and is difficult to characterize because the 1 mmol/L), but not to KCl (40 mmol/L), indicating activity at offending snake is often not identified.3,5 However, symptoms of post-synaptic nicotinic receptors on the skeletal muscle. -
Hollow-Bearing Trees As a Habitat Resource Along an Urbanisation Gradient
Hollow-Bearing Trees as a Habitat Resource along an Urbanisation Gradient Author Treby, Donna Louise Published 2014 Thesis Type Thesis (PhD Doctorate) School Griffith School of Environment DOI https://doi.org/10.25904/1912/1674 Copyright Statement The author owns the copyright in this thesis, unless stated otherwise. Downloaded from http://hdl.handle.net/10072/367782 Griffith Research Online https://research-repository.griffith.edu.au Hollow-bearing Trees as a Habitat Resource along an Urbanisation Gradient Donna Louise Treby MPhil (The University of Queensland) Environmental Futures Centre. Griffith School of Environment, Griffith University, Gold Coast. A thesis submitted for the fulfilment for the requirements of the degree of Doctor of Philosophy. December 2013. “If we all did the things we are capable of doing. We would literally live outstanding lives. I think; if we all lived our lives this way, we would truly create an amazing world.” Thomas Edison. i Acknowledgements: It would be remiss of me if I did not begin by acknowledging my principal supervisor Dr Guy Castley, for the inception, development and assistance with the completion of this study. Your generosity, open door policy and smiling face made it a pleasure to work with you. I owe you so much, but all I can give you is my respect and heartfelt thanks. Along with my associate supervisor Prof. Jean-Marc Hero their joint efforts inspired me and opened my mind to the complexities and vagaries of ecological systems and processes on such a large scale. To my volunteers in the field, Katie Robertson who gave so much of her time and help in the early stages of my project, Agustina Barros, Ivan Gregorian, Sally Healy, Guy Castley, Katrin Lowe, Kieran Treby, Phil Treby, Erin Wallace, Nicole Glenane, Nick Clark, Mark Ballantyne, Chris Tuohy, Ryan Pearson and Nickolas Rakatopare all contributed to the collection of data for this study. -
Koolan Island Quoll Demographics & Genetics
Running head: Conservation status of the Olive Python Final report GENETIC SURVEY OF THE PILBARA OLIVE PYTHON (Liasis olivaceaus barroni) David Pearson1, Peter Spencer2 Mia Hillyer2 and Ric A. How3 1Science Division, Department of Parks and Wildlife PO Box 51, Wannerooo, WA 6946 2School of Veterinary and Life Sciences, Murdoch University 90 South St, Murdoch, WA 6150 3Department of Terrestrial Zoology (Vertebrates), Western Australian Museum, 49 Kew St, Welshpool, WA 6986 September, 2013 Olive python – final report 1 Running head: Conservation status of the Olive Python Summary • The study used genetic information to investigate differences between and within populations of olive pythons in the Pilbara. This information was compared with genetic profiles from olive pythons form the Kimberley and carpet pythons. • Genetic variation was examined at eight nuclear genes (microsatellite) from 47 individual olive pythons. • Genetic analyses of nuclear markers show that the Pilbara olive python contains low levels of diversity, compared with its Kimberley counterpart. • The Pilbara population also had a low effective population size, but showed no signatures of a genetic bottleneck as a result of a population crash. • Nuclear DNA markers identified two distinct olive python populations. One in the Pilbara and the other in the Kimberley. • Mitochondrial analysis at three diagnostic regions showed two distinct clades representing Pilbara and Kimberley olive pythons, exclusively, consistent with results from nuclear markers. • Overall olive pythons appear to have two Evolutionary Significant Units. The Pilbara unit appear to be less genetically diverse than Kimberley one and shows little phylogeographic structure within the Pilbara. • There is sufficient evidence from the data that the taxonomy of the two groups should be subject to a re-appraisal, the Kimberley and Pilbara Olive pythons sufficiently different to be considered as different species. -
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. -
Bibliography and Scientific Name Index to Amphibians
lb BIBLIOGRAPHY AND SCIENTIFIC NAME INDEX TO AMPHIBIANS AND REPTILES IN THE PUBLICATIONS OF THE BIOLOGICAL SOCIETY OF WASHINGTON BULLETIN 1-8, 1918-1988 AND PROCEEDINGS 1-100, 1882-1987 fi pp ERNEST A. LINER Houma, Louisiana SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE NO. 92 1992 SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE The SHIS series publishes and distributes translations, bibliographies, indices, and similar items judged useful to individuals interested in the biology of amphibians and reptiles, but unlikely to be published in the normal technical journals. Single copies are distributed free to interested individuals. Libraries, herpetological associations, and research laboratories are invited to exchange their publications with the Division of Amphibians and Reptiles. We wish to encourage individuals to share their bibliographies, translations, etc. with other herpetologists through the SHIS series. If you have such items please contact George Zug for instructions on preparation and submission. Contributors receive 50 free copies. Please address all requests for copies and inquiries to George Zug, Division of Amphibians and Reptiles, National Museum of Natural History, Smithsonian Institution, Washington DC 20560 USA. Please include a self-addressed mailing label with requests. INTRODUCTION The present alphabetical listing by author (s) covers all papers bearing on herpetology that have appeared in Volume 1-100, 1882-1987, of the Proceedings of the Biological Society of Washington and the four numbers of the Bulletin series concerning reference to amphibians and reptiles. From Volume 1 through 82 (in part) , the articles were issued as separates with only the volume number, page numbers and year printed on each. Articles in Volume 82 (in part) through 89 were issued with volume number, article number, page numbers and year. -
Venemous Snakes
WASAH WESTERN AUSTRALIAN SOCIETY of AMATEUR HERPETOLOGISTS (Inc) K E E P I N G A D V I C E S H E E T Venomous Snakes Southern Death Adder (Acanthophis Southern Death antarcticus) – Maximum length 100 cm. Adder Category 5. Desert Death Adder (Acanthophis pyrrhus) – Acanthophis antarcticus Maximum length 75 cm. Category 5. Pilbara Death Adder (Acanthophis wellsi) – Maximum length 70 cm. Category 5. Western Tiger Snake (Notechis scutatus) - Maximum length 160 cm. Category 5. Mulga Snake (Pseudechis australis) – Maximum length 300 cm. Category 5. Spotted Mulga Snake (Pseudechis butleri) – Maximum length 180 cm. Category 5. Dugite (Pseudonaja affinis affinis) – Maximum Desert Death Adder length 180 cm. Category 5. Acanthophis pyrrhus Gwardar (Pseudonaja nuchalis) – Maximum length 100 cm. Category 5. NOTE: All species listed here are dangerously venomous and are listed as Category 5. Only the experienced herpetoculturalist should consider keeping any of them. One must be over 18 years of age to hold a category 5 license. Maintaining a large elapid carries with 1 it a considerable responsibility. Unless you are Pilbara Death Adder confident that you can comply with all your obligations and licence requirements when Acanthophis wellsi keeping dangerous animals, then look to obtaining a non-venomous species instead. NATURAL HABITS: Venomous snakes occur in a wide variety of habitats and, apart from death adders, are highly mobile. All species are active day and night. HOUSING: In all species listed except death adders, one adult (to 150 cm total length) can be kept indoors in a lockable, top-ventilated, all glass or glass-fronted wooden vivarium of Western Tiger Snake at least 90 x 45 cm floor area. -
Dendrelaphis Pictus (GMELIN, 1789) Complex – 2
HERPETOZOA 21 (1/2): 3 - 29 3 Wien, 30. Juni 2008 Contributions to a review of the Dendrelaphis pictus (GMELIN, 1789) complex – 2. the eastern forms (Serpentes: Colubridae) Beiträge zu einer Revision des Dendrelaphis pictus (GMELIN, 1789) Komplexes – 2. die östlichen Formen (Serpentes: Colubridae) GERNOT VOGEL & JOHAN VAN ROOIJEN KURZFASSUNG Die südostasiatischen, indonesischen und philippinischen Formen der polytypischen Art Dendrelaphis pic- tus (GMELIN, 1789) werden mit Hilfe der Multivariationsanalyse untersucht. Mehrere phänetisch unterschiedliche Cluster sind erkennbar. Geografisch werden diese Cluster durch wichtige biogeographische Barrieren wie zum Beispiel der Isthmus von Kra, die Wallace Linie und die Weber Linie getrennt. Die indochinesischen und die Sunda-Populationen werden trotz morphologischer Unterschiede zwischen ihnen unter dem Namen D. pictus zusammengefaßt, da sie als nicht voneinander unabhängig betrachtet werden. Zwei weitere Cluster werden als eigenständige Arten betrachtet, da diese Populationen ohne Zweifel unabhängige evolutionäre Linien bilden. Der erste dieser Cluster umfaßt die Populationen der Philippinen und Sulawesis. Diese Populationen werden unter dem Namen D. marenae beschrieben. Diese Art unterscheidet sich von den bisher benannten Formen in der Färbung, der Größe der Vertebralschuppen, der Anzahl der Subcaudalia und der Schwanzlänge. Der zweite Cluster umfaßt die Populationen der Molukken, welche mit dem Namen D. grismeri belegt werden. Diese Art zeichnet sich durch die Anzahl der Ventralia, Subcaudalia und Temporalia sowie die Schwanzlänge aus. ABSTRACT The Southeast Asian, Indonesian and Philippine forms of the polytypic Dendrelaphis pictus (GMELIN, 1789) are reviewed using multivariate analyses. Several distinct phenetic clusters are discerned. Geographically, these clusters are separated by important biogeographic boundaries, such as the Isthmus of Kra, Wallace’s line and Weber’s line. -
Snakes of South-East Asia Including Myanmar, Thailand, Malaysia, Singapore, Sumatra, Borneo, Java and Bali
A Naturalist’s Guide to the SNAKES OF SOUTH-EAST ASIA including Myanmar, Thailand, Malaysia, Singapore, Sumatra, Borneo, Java and Bali Indraneil Das First published in the United Kingdom in 2012 by Beaufoy Books n n 11 Blenheim Court, 316 Woodstock Road, Oxford OX2 7NS, England Contents www.johnbeaufoy.com 10 9 8 7 6 5 4 3 2 1 Introduction 4 Copyright © 2012 John Beaufoy Publishing Limited Copyright in text © Indraneil Das Snake Topography 4 Copyright in photographs © [to come] Dealing with Snake Bites 6 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without the prior written permission of the publishers. About this Book 7 ISBN [to come] Glossary 8 Edited, designed and typeset by D & N Publishing, Baydon, Wiltshire, UK Printed and bound [to come] Species Accounts and Photographs 11 Checklist of South-East Asian Snakes 141 Dedication Nothing would have happened without the support of the folks at home: my wife, Genevieve V.A. Gee, and son, Rahul Das. To them, I dedicate this book. Further Reading 154 Acknowledgements 155 Index 157 Edited and designed by D & N Publishing, Baydon, Wiltshire, UK Printed and bound in Malaysia by Times Offset (M) Sdn. Bhd. n Introduction n n Snake Topography n INTRODUCTION Snakes form one of the major components of vertebrate fauna of South-East Asia. They feature prominently in folklore, mythology and other belief systems of the indigenous people of the region, and are of ecological and conservation value, some species supporting significant (albeit often illegal) economic activities (primarily, the snake-skin trade, but also sale of meat and other body parts that purportedly have medicinal properties). -
An Overview and Checklist of the Native and Alien Herpetofauna of the United Arab Emirates
Herpetological Conservation and Biology 5(3):529–536. Herpetological Conservation and Biology Symposium at the 6th World Congress of Herpetology. AN OVERVIEW AND CHECKLIST OF THE NATIVE AND ALIEN HERPETOFAUNA OF THE UNITED ARAB EMIRATES 1 1 2 PRITPAL S. SOORAE , MYYAS AL QUARQAZ , AND ANDREW S. GARDNER 1Environment Agency-ABU DHABI, P.O. Box 45553, Abu Dhabi, United Arab Emirates, e-mail: [email protected] 2Natural Science and Public Health, College of Arts and Sciences, Zayed University, P.O. Box 4783, Abu Dhabi, United Arab Emirates Abstract.—This paper provides an updated checklist of the United Arab Emirates (UAE) native and alien herpetofauna. The UAE, while largely a desert country with a hyper-arid climate, also has a range of more mesic habitats such as islands, mountains, and wadis. As such it has a diverse native herpetofauna of at least 72 species as follows: two amphibian species (Bufonidae), five marine turtle species (Cheloniidae [four] and Dermochelyidae [one]), 42 lizard species (Agamidae [six], Gekkonidae [19], Lacertidae [10], Scincidae [six], and Varanidae [one]), a single amphisbaenian, and 22 snake species (Leptotyphlopidae [one], Boidae [one], Colubridae [seven], Hydrophiidae [nine], and Viperidae [four]). Additionally, we recorded at least eight alien species, although only the Brahminy Blind Snake (Ramphotyplops braminus) appears to have become naturalized. We also list legislation and international conventions pertinent to the herpetofauna. Key Words.— amphibians; checklist; invasive; reptiles; United Arab Emirates INTRODUCTION (Arnold 1984, 1986; Balletto et al. 1985; Gasperetti 1988; Leviton et al. 1992; Gasperetti et al. 1993; Egan The United Arab Emirates (UAE) is a federation of 2007). -
Spatial Ecology of the Oregon Gartersnake, Thamnophis Atratus Hydrophilus, in a Free-Flowing Stream Environment
Copeia 2010, No. 1, 75–85 Spatial Ecology of the Oregon Gartersnake, Thamnophis atratus hydrophilus, in a Free-Flowing Stream Environment Hartwell H. Welsh, Jr.1, Clara A. Wheeler1, and Amy J. Lind2 Spatial patterns of animals have important implications for population dynamics and can reveal other key aspects of a species’ ecology. Movements and the resulting spatial arrangements have fitness and genetic consequences for both individuals and populations. We studied the spatial and dispersal patterns of the Oregon Gartersnake, Thamnophis atratus hydrophilus, using capture–recapture techniques. Snakes showed aggregated dispersion. Frequency distributions of movement distances were leptokurtic; the degree of kurtosis was highest for juvenile males and lowest for adult females. Males were more frequently recaptured at locations different from their initial capture sites, regardless of age class. Dispersal of neonates was not biased, whereas juvenile and adult dispersal were male-biased, indicating that the mechanisms that motivate individual movements differed by both age class and sex. Males were recaptured within shorter time intervals than females, and juveniles were recaptured within shorter time intervals than adults. We attribute differences in capture intervals to higher detectability of males and juveniles, a likely consequence of their greater mobility. The aggregated dispersion appears to be the result of multi-scale habitat selection, and is consistent with the prey choices and related foraging strategies exhibited by the different age classes. Inbreeding avoidance in juveniles and mate-searching behavior in adults may explain the observed male-biased dispersal patterns. ULTIPLE interacting factors may affect the resources such as food, basking sites, hibernacula or mates movements and resulting spatial patterns of (Gregory et al., 1987). -
Death Adders {Acanthophis Laevis Complex) from the Island of Ambon
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Herpetozoa Jahr/Year: 2006 Band/Volume: 19_1_2 Autor(en)/Author(s): Kuch Ulrich, McGuire Jimmy A., Yuwono Frank Bambang Artikel/Article: Death adders (Acanthophis laevis complex) from the island of Ambon (Maluku, Indonesia) 81-82 ©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 81 O. & PINTO, I. & BRUFORD, M. W. & JORDAN, W. C. & NICHOLS, R. A. (2002): The double origin of Iberian peninsular chameleons.- Biological Journal of the Linnean Society, London; 75: 1-7. PINHO, C. & FER- RAND, N. & HARRIS, D. J. (2006): Reexamination of the Iberian and North African Podarcis phylogeny indi- cates unusual relative rates of mitochondrial gene evo- lution in reptiles.- Molecular Phylogenetics and Evolu- tion, Chicago; 38: 266-273. POSADA, D. &. CRANDALL, K. A. (1998): Modeltest: testing the model of DNA substitution- Bioinformatics, Oxford; 14: 817-818. SWOFFORD, D. L. (2002): PAUP*. Phylogenetic analy- sis using parsimony (*and other methods). Version 4.0. Sinauer Associates, Uderland, Massachusetts. WADK, E. (2001): Review of the False Smooth snake genus Macroprotodon (Serpentes, Colubridae) in Algeria with a description of a new species.- Bulletin National Fig. 1 : Adult death adder (Acanthophis laevis com- History Museum London (Zoology), London; 67 (1): plex) from Negeri Lima, Ambon (Central Maluku 85-107. regency, Maluku province, Indonesia). Photograph by U. KUCH. KEYWORDS: mitochondrial DNA, cyto- chrome b, Macroprotodon, evolution, systematics, Iberian Peninsula, North Africa SUBMITTED: April 1,2005 and Bali by the live animal trade. -
Jemena Northern Gas Pipeline Pty Ltd
Jemena Northern Gas Pipeline Pty Ltd Northern Gas Pipeline Draft Environmental Impact Statement CHAPTER 12 – MATTERS OF NATIONAL ENVIRONMENTAL SIGNIFICANCE Public August 2016 MATTERS OF NATIONAL ENVIRONMENTAL SIGNIFICANCE — 12 Contents 12. Matters of National Environmental Significance ............................................................. 12-1 12.1 Overview .................................................................................................................... 12-1 12.2 Relevant MNES ......................................................................................................... 12-2 12.2.1 Threatened species ............................................................................................ 12-2 12.2.2 Plains Death Adder (Acanthophis hawkei) ........................................................ 12-13 12.2.3 Carpentarian Antechinus (Pseudantechinus mimulus) ...................................... 12-18 12.2.4 Threatened species conclusion ......................................................................... 12-23 12.3 Risk assessment ...................................................................................................... 12-23 12.3.1 Potential impacts .............................................................................................. 12-23 12.3.2 Planning ............................................................................................................ 12-24 12.3.3 Construction ....................................................................................................