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												  Sea Snakes Lose Their Stripes to Deal with Pollution : Nature NewsNATURE | NEWS Sea snakes lose their stripes to deal with pollution Melanin pigment in darkened skin binds to pollutants and helps animals rid themselves of chemicals. Rachael Lallensack 10 August 2017 Klaus Stiefel The melanin pigment in the turtle-headed sea snake's dark bands binds to pollutants. Sea snakes that live in polluted waters have evolved to ‘fill in’ their light stripes, darkening their skins to cope with pollution. The finding1 adds turtle-headed sea snakes (Emydocephalus annulatus) to the diverse list of creatures that exhibit ‘industrial melanism’, when darker animal varieties become dominant in polluted environments. The phenomenon is a classic example of natural selection, and one of the best-known cases — the spread of the dark version of the peppered moth in sooty nineteenth-century Britain — is often quoted in biology textbooks. For decades, evolutionary ecologist Rick Shine has snorkelled in the bays of Nouméa in the South Pacific island of New Caledonia to study the sea snake species and collect their shed skins. Over the years, while studying the Related stories Related stories snakes in the Indo–Pacific, he • Dark satanic wings • Dark satanic wings noticed something curious: in some populations, most snakes were jet • Evolution sparks silence • Evolution sparks silence black, whereas in others, most of the crickets of the crickets sported pale banding or blotchy • The peppered moth's • The peppered moth's white markings. dark genetic past dark genetic past revealed revealed In 2014, Claire Goiran, a marine biologist at the University of New More related stories More related stories Caledonia in Nouméa who sometimes helped Shine to collect sea snakes, came across a study about Parisian pigeons2.
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												  Morphology, Reproduction and Diet of the Greater Sea Snake, Hydrophis Major (Elapidae, Hydrophiinae)Coral Reefs https://doi.org/10.1007/s00338-019-01833-5 REPORT Morphology, reproduction and diet of the greater sea snake, Hydrophis major (Elapidae, Hydrophiinae) 1 1 2 R. Shine • T. Shine • C. Goiran Received: 5 January 2019 / Accepted: 9 June 2019 Ó Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract Although widespread, the large Hydrophiinae relatives in some respects, other characteristics (such as sea snake Hydrophis major is poorly known ecologically. scale rugosity, low proportion of juveniles in collections, We dissected 119 preserved specimens in museum col- frequent production of small litters of large offspring) may lections to quantify body sizes and proportions, sexual reflect adaptation to marine habitats. dimorphism, reproductive biology and diet. The sexes mature at similar snout–vent lengths (SVLs, about 75 cm) Keywords Dietary specialisation Á Disteira major Á and attain similar maximum sizes (females 123 cm vs. Elapidae Á Life-history Á Olive-headed sea snake Á Trophic males 122 cm SVL), but females in our sample exhibited ecology larger mean sizes than did males (means 98.8 vs. 93.1 cm SVL). The adult sex ratio in museum specimens was highly female-biased (64:30), and the high proportion of repro- Introduction ductive females during the austral summer suggests annual reproduction. At the same SVL, females had shorter tails Rates of speciation are higher in the viviparous sea snakes and wider bodies than did males, but sex differences in (Hydrophiinae) than in any other extant group of reptiles. other body proportions (e.g. tail shape, head dimensions, In particular, one clade of sea snakes—the Hydrophis eye diameter) were minimal.
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												  The Herpetological JournalVolume 8, Number 3 July 1998 ISSN 0268-0130 THE HERPETOLOGICAL JOURNAL Published by the Indexed in BRITISH HERPETOLOGICAL SOCIETY Current Contents Th e Herpetological Jo urnal is published quarterly by the British Herpetological Society and is issued freeto members. Articles are listed in Current Awareness in Biological Sciences, Current Contents, Science Citation Index and Zoological Record. Applications to purchase copies and/or for details of membership should be made to the Hon. Secretary, British Herpetological Society, The Zoological Society of London, Regent's Park, London NWl 4RY, UK. Instructions to authors are printed inside the back cover. All contributions should be addressed to the Editor (address below). Editor: Richard A. Griffiths, The Durrell Institute of Conservation and Ecology, University of Kent, Canterbury, Kent CT2 7NJ, UK Associate Editor: Leigh Gillett Editorial Board: Pim Arntzen (Oporto) Donald Broadley (Zimbabwe) John Cooper (Wellingborough) John Davenport (Millport) Andrew Gardner (Oman) Tim Halliday (Milton Keynes) Michael Klemens (New York) Colin McCarthy (London) Andrew Milner (London) Henk Strijbosch (Nijmegen) Richard Tinsley (Bristol) BRITISH HERPETOLOGICAL SOCIETY Copyright It is a fundamental condition that submitted manuscripts have not been published and will not be simultaneously submitted or published elsewhere. By submitting a manuscript, the authors agree that the copyright for their article is transferred to the publisher if and when the article is accepted for publication. The copyright covers the exclusive rights to reproduce and distribute the article, including reprints and photographic reproductions. Permission for any such activities must be sought in advance from the Editor. ADVERTISEMENTS The Herpetological Journal accepts advertisements subject to approval of contents by the Editor, to whom enquiries should be addressed.
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												  Australasian Journal of Herpetology ISSN 1836-5698 (Print)1 Issue 12, 30 April 2012 ISSN 1836-5779 (Online) Australasian Journal of HerpetologyAustralasian Journal of Herpetology ISSN 1836-5698 (Print)1 Issue 12, 30 April 2012 ISSN 1836-5779 (Online) Australasian Journal of Herpetology Hoser 2012 - Australasian Journal of Herpetology 9:1-64. Available online at www.herp.net Contents on pageCopyright- 2. Kotabi Publishing - All rights reserved 2 Australasian Journal of Herpetology Issue 12, 30 April 2012 Australasian Journal of Herpetology CONTENTS ISSN 1836-5698 (Print) ISSN 1836-5779 (Online) A New Genus of Coral Snake from Japan (Serpentes:Elapidae). Raymond T. Hoser, 3-5. A revision of the Asian Pitvipers, referred to the genus Cryptelytrops Cope, 1860, with the creation of a new genus Adelynhoserea to accommodate six divergent species (Serpentes:Viperidae:Crotalinae). Raymond T. Hoser, 6-8. A division of the South-east Asian Ratsnake genus Coelognathus (Serpentes: Colubridae). Raymond T. Hoser, 9-11. A new genus of Asian Snail-eating Snake (Serpentes:Pareatidae). Raymond T. Hoser, 10-12-15. The dissolution of the genus Rhadinophis Vogt, 1922 (Sepentes:Colubrinae). Raymond T. Hoser, 16-17. Three new species of Stegonotus from New Guinea (Serpentes: Colubridae). Raymond T. Hoser, 18-22. A new genus and new subgenus of snakes from the South African region (Serpentes: Colubridae). Raymond T. Hoser, 23-25. A division of the African Genus Psammophis Boie, 1825 into 4 genera and four further subgenera (Serpentes: Psammophiinae). Raymond T. Hoser, 26-31. A division of the African Tree Viper genus Atheris Cope, 1860 into four subgenera (Serpentes:Viperidae). Raymond T. Hoser, 32-35. A new Subgenus of Giant Snakes (Anaconda) from South America (Serpentes: Boidae). Raymond T. Hoser, 36-39.
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												  A Division of the African Tree Viper Genus Atheris Cope, 1860 Into Four Subgenera (Serpentes:Viperidae)32 Australasian Journal of Herpetology Australasian Journal of Herpetology 12:32-35. ISSN 1836-5698 (Print) ISSN 1836-5779 (Online) Published 30 April 2012. A division of the African Tree Viper genus Atheris Cope, 1860 into four subgenera (Serpentes:Viperidae). Raymond T. Hoser 488 Park Road, Park Orchards, Victoria, 3114, Australia. Phone: +61 3 9812 3322 Fax: 9812 3355 E-mail: [email protected] Received 15 February 2012, Accepted 2 April 2012, Published 30 April 2012. ABSTRACT The African Tree Viper genus Atheris has been of interest to taxonomists in recent years. Significant was the removal of the species superciliaris to the newly created monotypic genus Proatheris and the species hindii to the monotypic genus Montatheris both by Broadley in 1996 gaining widespread acceptance. Marx and Rabb (1965), erected a monotypic genus Adenorhinos for the species barbouri, but this designation has not gained widespread support from other herpetologists, with a number of recent classifications continuing to place the taxon within Atheris (e.g. Menegon et. al. 2011). Phylogenetic studies of the genus Atheris senso lato using molecular methods (e.g. Pyron et. al. 2011) have upheld the validity of the creation of the monotypic genera Proatheris and Montatheris by Broadley. These studies have also shown there to be at least four well-defined groups of species within the genus Atheris as recognized in early 2012, though not as divergent as seen for the snakes placed within Proatheris and Montatheris. As a result, the genus is now subdivided into subgenera using available names for three, with the fourth one being named Woolfvipera subgen.
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												  A Phylogeny and Revised Classification of Squamata, Including 4161 Species of Lizards and SnakesBMC Evolutionary Biology This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes BMC Evolutionary Biology 2013, 13:93 doi:10.1186/1471-2148-13-93 Robert Alexander Pyron ([email protected]) Frank T Burbrink ([email protected]) John J Wiens ([email protected]) ISSN 1471-2148 Article type Research article Submission date 30 January 2013 Acceptance date 19 March 2013 Publication date 29 April 2013 Article URL http://www.biomedcentral.com/1471-2148/13/93 Like all articles in BMC journals, this peer-reviewed article can be downloaded, printed and distributed freely for any purposes (see copyright notice below). Articles in BMC journals are listed in PubMed and archived at PubMed Central. For information about publishing your research in BMC journals or any BioMed Central journal, go to http://www.biomedcentral.com/info/authors/ © 2013 Pyron et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes Robert Alexander Pyron 1* * Corresponding author Email: [email protected] Frank T Burbrink 2,3 Email: [email protected] John J Wiens 4 Email: [email protected] 1 Department of Biological Sciences, The George Washington University, 2023 G St.
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												  The Status of Marine Reptiles in New South WalesThe Status of Marine Reptiles in New South Wales A Report prepared for the New South Wales National Parks and Wildlife Service by Dr Harold G. Cogger _________ Cogger Consulting Services P/L Table of Contents Executive Summary ………………………………………………………………………………... 3 1. Introduction ……………………………………………………………………………………… 5 2, The conservation status of marine reptiles in NSW: assessment criteria and their significance …………………………….……………………………………… 8 3. Methodology …………………………………………………………………………………..… 9 4. Data Sources ………………………………………………………………………………...… 10 5. Major threatening processes with the potential to impact on marine reptiles ……...10 6. Annotated List of Species of Marine Reptiles recorded from NSW ……………..…… 13 7. Marine Turtles ………..……………………………………………………………………..… 14 Chelonia mydas (Green Turtle) …………………………………...………………..…… 14 Natator depressus (Flatback Turtle) ……………………………………………………. 16 Caretta caretta (Loggerhead Turtle) ……………………………………………………..17 Eretmochelys imbricata (Hawksbill Turtle ………………………………….………….. 19 Dermochelys coriacea (Leathery or Luth Turtle) ……………………………..……….. 20 8. Marine Snakes ……………………………………………………………………………...… 21 Acalyptophis peronii ………………………………………...……………………………. 22 Aipysurus duboisii ………………………………………………………………………… 23 Aipysurus laevis …………………………………………………..………………………. 24 Astrotia stokesii ……………………………………………………...……………………. 25 Disteira kingii …………………………………………………………..………………….. 26 Disteria major …………………………………………………………..…………………. 27 Emydocephalus annulatus ………………………………………………………….…… 28 Hydrophis elegans …………………………………………………………..…….….….. 29
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												  Browsing by the Sea Snake Emydocephalus AnnulatusFunctional Blackwell Publishing, Ltd. Ecology 2004 A novel foraging mode in snakes: browsing by the sea snake 18, 16–24 Emydocephalus annulatus (Serpentes, Hydrophiidae) R. SHINE,† X. BONNET, M. J. ELPHICK and E. G. BARROTT Biological Sciences A08, University of Sydney, New South Wales 2006, Australia Summary 1. Ecologists often ascribe considerable importance to traits that are widespread within a specific lineage but rarely seen in other kinds of organisms. Unfortunately, such hypotheses cannot be tested robustly unless there is variation in expression of the trait within that lineage; such ‘exceptions to the rule’ provide opportunities to falsify predictions about putative functional correlates of the focal trait. 2. Research on snake foraging has emphasized species that feed infrequently and take large prey, often from ambush positions, but these characteristics do not apply to all snakes. 3. Movement patterns and feeding rates of free-ranging Turtle-Headed Sea Snakes Emydocephalus annulatus (Krefft 1869) were quantified in coral reefs of New Caledonia. These snakes forage by moving slowly (<2 m min−1) but consistently across the sub- strate as they investigate crevices and burrows for fish nests. The snakes feed frequently (sometimes, several times per hour) on large numbers of very small (1 × 0·5 mm2) eggs. Snakes weighed more than one hundred thousand times as much as the prey items (eggs) they consumed, in contrast to high relative prey masses often reported for other snake species. 4. Field experiments in which snakes were exposed to a variety of stimuli indicate that these animals locate their prey by scent rather than visual cues.
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												  Patterns of Species Richness, Endemism and Environmental Gradients of African ReptilesJournal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Patterns of species richness, endemism ARTICLE and environmental gradients of African reptiles Amir Lewin1*, Anat Feldman1, Aaron M. Bauer2, Jonathan Belmaker1, Donald G. Broadley3†, Laurent Chirio4, Yuval Itescu1, Matthew LeBreton5, Erez Maza1, Danny Meirte6, Zoltan T. Nagy7, Maria Novosolov1, Uri Roll8, 1 9 1 1 Oliver Tallowin , Jean-Francßois Trape , Enav Vidan and Shai Meiri 1Department of Zoology, Tel Aviv University, ABSTRACT 6997801 Tel Aviv, Israel, 2Department of Aim To map and assess the richness patterns of reptiles (and included groups: Biology, Villanova University, Villanova PA 3 amphisbaenians, crocodiles, lizards, snakes and turtles) in Africa, quantify the 19085, USA, Natural History Museum of Zimbabwe, PO Box 240, Bulawayo, overlap in species richness of reptiles (and included groups) with the other ter- Zimbabwe, 4Museum National d’Histoire restrial vertebrate classes, investigate the environmental correlates underlying Naturelle, Department Systematique et these patterns, and evaluate the role of range size on richness patterns. Evolution (Reptiles), ISYEB (Institut Location Africa. Systematique, Evolution, Biodiversite, UMR 7205 CNRS/EPHE/MNHN), Paris, France, Methods We assembled a data set of distributions of all African reptile spe- 5Mosaic, (Environment, Health, Data, cies. We tested the spatial congruence of reptile richness with that of amphib- Technology), BP 35322 Yaounde, Cameroon, ians, birds and mammals. We further tested the relative importance of 6Department of African Biology, Royal temperature, precipitation, elevation range and net primary productivity for Museum for Central Africa, 3080 Tervuren, species richness over two spatial scales (ecoregions and 1° grids). We arranged Belgium, 7Royal Belgian Institute of Natural reptile and vertebrate groups into range-size quartiles in order to evaluate the Sciences, OD Taxonomy and Phylogeny, role of range size in producing richness patterns.
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												  Snake Venom Potency and Yield Are Associated with Prey-Evolution, Predator Metabolism and Habitat StructureSnake venom potency and yield are associated with prey-evolution, predator metabolism and habitat structure Kevin Healy a, b, c, *, Chris Carbone d and Andrew L. Jackson a. a Department of Zoology, School of Natural Sciences, Trinity College Dublin, Dublin 2, Ireland. b School of Biology, University of St Andrews, St Andrews KY16 9TH, UK. c School of Natural Sciences, National University of Ireland Galway, Galway, Republic of Ireland. d Institute of Zoology, Zoological Society of London, London, UK * Corresponding author: [email protected], School of Biology, University of St Andrews, St Andrews KY16 9TH, UK. Short running title Macroecological factors drive venom evolution Article type: Letters Number of words in abstract: 150 Number of words in main text: 4984 Number of references: 73 Number of Figures: 4 Statement of authorship KH collated the dataset and conducted the analysis. All authors contributed to the analysis, design, discussion and interpretation of the results, and writing of the manuscript. Data accessibility statement Data available from the Figshare Digital Repository https://doi.org/10.6084/m9.figshare.7128566.v1 Keywords Venom, Body size, Comparative analysis, Scaling, trophic ecology, Macroecology, LD50, Phylogenetic analysis, Snake, Abstract Snake venom is well known for its ability to incapacitate and kill prey. Yet, potency and the amount of venom available varies greatly across species, ranging from the seemingly harmless to those capable of killing vast numbers of potential prey. This variation is poorly understood, with comparative approaches confounded by the use of atypical prey species as models to measure venom potency. Here, we account for such confounding issues by incorporating the phylogenetic similarity between a snake’s diet and the species used to measure its potency.
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												  The Conservation Status of Marine Elapid SnakesHerpetological Conservation and Biology 8(1): 37 – 52. Submitted:1 August 2012; Accepted: 7 January 2013; Published: 30 April 2013. FASCINATING AND FORGOTTEN: THE CONSERVATION STATUS OF MARINE ELAPID SNAKES 1,2 3,4 5 CRISTIANE T. ELFES SUZANNE R. LIVINGSTONE , AMANDA LANE , VIMOKSALEHI 6,7 8 9 10 LUKOSCHE , KATE L. SANDERS , ANTHONY J. COURTNEY , JOEY L. GATUS , MICHAEL 11 12 13 14 15 GUINEA , AARON S. LOBO , DAVID MILTON , ARNE R. RASMUSSEN , MARK READ , 16 17 18 19 MAHREE-DEE WHITE , JONNELL SANCIANGCO , ANGEL ALCALA , HAROLD HEATWOLE , 20 20 21 4 DARYL R. KARNS , JEFFREY A. SEMINOFF , HAROLD K. VORIS , KENT E. CARPENTER , 21, 22 JOHN C. MURPHY 1Department of Ecology, Evolution and Marine Biology, University of California Santa Barbara, Santa Barbara, California 93106, USA 2IUCN Global Species Programme/Conservation International, Biodiversity Assessment Unit, 2011 Crystal Drive, Arlington, Virginia 22202, USA 3Department of Ecology and Environmental Biology, University of Glasgow, Glasgow, Scotland G128QQ 4IUCN Global Species Programme/Global Marine Species Assessment, Biological Sciences, Old Dominion University, Norfolk Virginia 23529, USA 5Faculty of Veterinary Science, University of Sydney, Sydney, New South Wales 2006, Australia 6Present address: ARC Center of Excellence for Coral Reef Studies, James Cook University, Townsville, Queensland 4811, Australia 7Department of Ecology and Evolutionary Biology, University of California, Irvine, California 92697, USA 8School of Earth and Environmental Sciences, University of Adelaide, Adelaide,
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												  Status of the World's Sea Snakes IUCN Red List AssessmentStatus of the World’s Sea Snakes IUCN Red List Assessment Final Report August 2009 IUCN Global Red List Assessment of Sea Snakes Workshop: 11‐14th February 2009 Brisbane, Australia Contact: Suzanne R Livingstone, PhD, Global Marine Species Assessment Email: [email protected] OR [email protected] Website: http://www.sci.odu.edu/gmsa/ 1. Contents Page 1. Contents 2 2. Acknowledgments 3 3. Project Rationale 3 4. Background 4 4.1. The Red List of Threatened Species 4 4.2. Global Marine Species Assessment 5 5. Methods 5 5.1. Data collection and IUCN Red List assessment process 5 5.2 IUCN Red List Categories 6 6. Results and Discussion 7 6.1. Sea snakes 7 6.2. Homalopsids 8 7. Conclusions 9 8. Reporting and outcomes 10 8.1. Results on the IUCN Red List of Threatened Species 10 8.2. Peer‐reviewed publications 10 8.3. Nominations for Australia’s EPBC Act 11 8.4. Creation of the IUCN Sea Snake Specialist Group 12 9. References 13 10. Appendices Appendix 1 ‐ workshop participants 14 Appendix 2 ‐ IUCN staff and project partners 15 Appendix 3 ‐ Sea snake species list and Red List Category 16 Appendix 4 ‐ Homalopsid snake species and Red List Category 18 2 2. Acknowledgements We would like to thank Dr Colin Limpus (Australian Government Environmental Protection Agency) and the International Sea Turtle Symposium committee for logistical and organizational support for the workshop. Special thanks to Jenny Chapman (EPA) and Chloe Schauble (ISTS). Thank you also to Dr Gordon Guymer (Chief Botanist – Director of Herbarium) for accommodating us at the Herbarium in the Brisbane Botanical Gardens.