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First Record of Laticauda Semifasciata (Reptilia: Squamata: Elapidae: Laticaudinae) from Korea
Anim. Syst. Evol. Divers. Vol. 32, No. 2: 148-152, April 2016 http://dx.doi.org/10.5635/ASED.2016.32.2.148 Short communication First Record of Laticauda semifasciata (Reptilia: Squamata: Elapidae: Laticaudinae) from Korea Jaejin Park1, Il-Hun Kim1,2, Kyo-Sung Koo1, Daesik Park3,* 1Department of Biology, Kangwon National University, Chuncheon 24341, Korea 2National Marine Biodiversity Institute of Korea, Seocheon 33661, Korea 3Division of Science Education, Kangwon National University, Chuncheon 24341, Korea ABSTRACT The Chinese sea snake Laticauda semifasciata (Reinwardt in Schlegel, 1837) is newly reported from Korean waters based on three specimens collected from Jeju Island, Korea, in August, September, and November 2015. This is the first time that the genus Laticauda and subfamily Laticaudinae has been reported from Korean waters. The subfamily Laticaudinae has ventrals that are four to five times wider than the adjacent dorsals, which are unlike the ventrals that are similar or up to two times wider than adjacent dorsals in the subfamily Hydrophiinae. Laticauda semifasciata is distinct from other species because it has three prefrontals and its rostrals are horizontally divided into two. As the result of this report, four species (L. semifasciata, Hydrophis (Pelamis) platurus, Hydrophis cyanocinctus, and H. melanocephalus) of sea snakes have been reported in Korean waters. Keywords: sea snake, Hydrophiinae, Laticaudinae, Chinese sea snake, Laticauda semifasciata INTRODUCTION semifasciata (Reinwardt in Schlegel, 1837) of the genus Laticauda and subfamily Laticaudinae for the first time in Globally, 70 sea snakes (aquatic elapids) of 8 genera in the Korean waters based on the specimens collected in Jeju Is- two subfamilies Hydrophiinae and Laticaudinae have been land in 2015. -
Herpetological Review
Herpetological Review FARANCIA ERYTROGRAMMA (Rainbow Snake). HABITAT. Submitted by STAN J. HUTCHENS (e-mail: [email protected]) and CHRISTOPHER S. DEPERNO, (e-mail: [email protected]), Fisheries and Wildlife Pro- gram, North Carolina State University, 110 Brooks Ave., Raleigh, North Carolina 27607, USA. canadensis) dams reduced what little fl ow existed in some canals to standing quagmires more representative of the habitat selected by Eastern Mudsnakes (Farancia abacura; Neill 1964, op. cit.). Interestingly, one A. rostrata was observed near BNS, but none was captured within the swamp. It is possible that Rainbow Snakes leave bordering fl uvial habitats in pursuit of young eels that wan- dered into canals and swamp habitats. Capturing such a secretive and uncommon species as F. ery- trogramma in unexpected habitat encourages consideration of their delicate ecological niche. Declining population indices for American Eels along the eastern United States are attributed to overfi shing, parasitism, habitat loss, pollution, and changes in major currents related to climate change (Hightower and Nesnow 2006. Southeast. Nat. 5:693–710). Eel declines could negatively impact population sizes and distributions of Rainbow Snakes, especially in inland areas. We believe future studies based on con- fi rmed Rainbow Snake occurrences from museum records or North Carolina GAP data could better delineate the range within North Carolina. Additionally, sampling for American Eels to determine their population status and distribution in North Carolina could augment population and distribution data for Rainbow Snakes. We thank A. Braswell, J. Jensen, and P. Moler for comments on earlier drafts of this manuscript. Submitted by STAN J. HUTCHENS (e-mail: [email protected]) and CHRISTOPHER S. -
A Comprehensive Report on the Hook-Nosed Sea Snake Enhydrina Schistosa (Daudin, 1803)
REPTILE RAP #18, 30 November 2016 A comprehensive report on the Hook-nosed Sea Snake Enhydrina schistosa (Daudin, 1803) Hatkar Prachi & Chinnasamy Ramesh* Wildlife Institute of India, Post Box # 18, Chandrabani, Dehradun, Uttarakhand 248001, India * [email protected] (corresponding author) Sea snakes (Hydrophiidae) form an important Act, 1972 (Whitaker et al. 2004). According to component of the coastal habitats of the tropical the IUCN red list, this species falls under Least and sub-tropical marine environment (Padate Concerned category. et al. 2009). Sea snakes spend most of their life Hook-nosed or Beaked sea snake (Enhydrina in the ocean but rarely come out to coastal land schistosa) is one of the commonest sea snakes (Damotharan et al. 2010). They are relatively found in India and other South-east Asian countries. abundant in estuaries and lagoons (Heatwole However, little is known about the distribution 1999; Valenta 2010). These poikilothermic scaly (site- specific records), ecology and natural history vertebrates are ovo-viviparous, respiring through of this species. Hence, the purpose of this paper lungs and fast swimmers in the sea but slow on land is (i) To report the further site-specific record of (Sedgwick 1905; Sharma 2003), comprising about this species from Maharashtra. (ii) To review and 86% of living marine reptile species (Damotharan compile the published information on this snake et al. 2010). They are known for one of the deadliest including negative interaction with humans, neurotoxic and myotoxic venom of all snakes and focusing on India’s coastal states and neighbouring valuable skin (O’Shea 2005). Though sea snakes countries to generate baseline information on are very common, detailed information on these E. -
Sea Snakes You Can Easily Change the Color Theme of Your Poster by Going to the Presentation Poster
(—THIS SIDEBAR DOES NOT PRINT—) QUICK START (cont.) DESIGN GUIDE How to change the template color theme This PowerPoint 2007 template produces a 36”x48” Sea Snakes You can easily change the color theme of your poster by going to the presentation poster. You can use it to create your research DESIGN menu, click on COLORS, and choose the color theme of your choice. You can also create your own color theme. poster and save valuable time placing titles, subtitles, text, and graphics. Howard Moon We provide a series of online tutorials that will guide you through the poster design process and answer your poster production questions. To view our template tutorials, go Abstract Venom Reproduction Diet You can also manually change the color of your background by going to online to PosterPresentations.com and click on HELP DESK. VIEW > SLIDE MASTER. After you finish working on the master be sure to Sea Snakes (also known as Hydrophiinae) are reptiles that Since sea snakes come from Elapidae family, the majority of Sea snakes are ovoviviparous, except for laticauda, which is Sea snakes are carnivores that feed on fish, fish eggs, go to VIEW > NORMAL to continue working on your poster. When you are ready to print your poster, go online to inhabit in marine environments that are considered one of the the Hydrophiinae species possess venom glands. Species oviparous. Although sea snakes are air-breathing species, they mollusks, eels, etc. They usually wander around the coral reefs How to add Text PosterPresentations.com most aquatic vertebrates. These guys are found in warm such as beaked sea snake (Enhydrina schistose) can kill about mate in water. -
Future Directions in the Research and Management of Marine Snakes
Charles Darwin University Future directions in the research and management of marine snakes Udyawer, Vinay; Barnes, Peter; Bonnet, Xavier; Brischoux, François; Crowe-Riddell, Jenna M.; D'Anastasi, Blanche; Fry, Bryan G.; Gillett, Amber; Goiran, Claire; Guinea, Michael L.; Heatwole, Harold; Heupel, Michelle R.; Hourston, Mathew; Kangas, Mervi; Kendrick, Alan; Koefoed, Inigo; Lillywhite, Harvey B.; Lobo, Aaron S.; Lukoschek, Vimoksalehi; McAuley, Rory; Nitschke, Charlotte; Rasmussen, Arne R.; Sanders, Kate L.; Sheehy, Coleman; Shine, Richard; Somaweera, Ruchira; Sweet, Samuel S.; Voris, Harold K. Published in: Frontiers in Marine Science DOI: 10.3389/fmars.2018.00399 Published: 06/11/2018 Document Version Publisher's PDF, also known as Version of record Link to publication Citation for published version (APA): Udyawer, V., Barnes, P., Bonnet, X., Brischoux, F., Crowe-Riddell, J. M., D'Anastasi, B., Fry, B. G., Gillett, A., Goiran, C., Guinea, M. L., Heatwole, H., Heupel, M. R., Hourston, M., Kangas, M., Kendrick, A., Koefoed, I., Lillywhite, H. B., Lobo, A. S., Lukoschek, V., ... Voris, H. K. (2018). Future directions in the research and management of marine snakes. Frontiers in Marine Science, 5, 1-16. [399]. https://doi.org/10.3389/fmars.2018.00399 General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. -
Volume 4 Issue 1B
Captive & Field Herpetology Volume 4 Issue 1 2020 Volume 4 Issue 1 2020 ISSN - 2515-5725 Published by Captive & Field Herpetology Captive & Field Herpetology Volume 4 Issue1 2020 The Captive and Field Herpetological journal is an open access peer-reviewed online journal which aims to better understand herpetology by publishing observational notes both in and ex-situ. Natural history notes, breeding observations, husbandry notes and literature reviews are all examples of the articles featured within C&F Herpetological journals. Each issue will feature literature or book reviews in an effort to resurface past literature and ignite new research ideas. For upcoming issues we are particularly interested in [but also accept other] articles demonstrating: • Conflict and interactions between herpetofauna and humans, specifically venomous snakes • Herpetofauna behaviour in human-disturbed habitats • Unusual behaviour of captive animals • Predator - prey interactions • Species range expansions • Species documented in new locations • Field reports • Literature reviews of books and scientific literature For submission guidelines visit: www.captiveandfieldherpetology.com Or contact us via: [email protected] Front cover image: Timon lepidus, Portugal 2019, John Benjamin Owens Captive & Field Herpetology Volume 4 Issue1 2020 Editorial Team Editor John Benjamin Owens Bangor University [email protected] [email protected] Reviewers Dr James Hicks Berkshire College of Agriculture [email protected] JP Dunbar -
WHO Guidance on Management of Snakebites
GUIDELINES FOR THE MANAGEMENT OF SNAKEBITES 2nd Edition GUIDELINES FOR THE MANAGEMENT OF SNAKEBITES 2nd Edition 1. 2. 3. 4. ISBN 978-92-9022- © World Health Organization 2016 2nd Edition All rights reserved. Requests for publications, or for permission to reproduce or translate WHO publications, whether for sale or for noncommercial distribution, can be obtained from Publishing and Sales, World Health Organization, Regional Office for South-East Asia, Indraprastha Estate, Mahatma Gandhi Marg, New Delhi-110 002, India (fax: +91-11-23370197; e-mail: publications@ searo.who.int). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader. In no event shall the World Health Organization be liable for damages arising from its use. -
Fluorescence Emission in a Marine Snake
Galaxea, Journal of Coral Reef Studies 21: 7-8(2019) Photogallery Fluorescence emission in a marine snake Takashi SEIKO and Yohey TERAI SOKENDAI (The Graduate University for Advanced Studies), Department of Evolutionary Studies of Biosystems, Shonan Village, Hayama, Kanagawa 240-0193, Japan. Corresponding authors: Y. Terai, T. Seiko Emails: [email protected]; [email protected] Communicated by Frederic Sinniger (Associate EditorsinChief) Keywords fluorescence, Laticauda, marine reptile, sea krait Coral reefs are one of the most colorful environments on Earth. Light in coral reefs includes fluorescence as well as reflectance of sunlight. In fluorescence, mole cules are excited by illuminating light and emit longer wavelength fluorescence than the excitation light wave length. In coral reefs, fluorescent light emission is observed in a range of taxa including cnidarians (e.g. corals), arthropods and fishes (e.g., Johnsen 2012). In marine reptiles, fluorescent emission has reported thus far only from sea turtles (Gruber and Sparks 2015). Here we report fluorescent light emission in a marine snake. Laticauda laticaudata Linnaeus, 1758 is a semi aquatic sea krait (Elapidae: Laticaudinae) often ob served in coral reefs. We examined a specimen that was freshly frozen after death and subsequently thawed. This speci men was caught at Oganzaki, Ishigaki island, Oki nawa, Japan (24°27′12.4″N; 124°04′37.4″E) Fig. 1 Photographs of a sea krait (Laticauda laticaudata) illuminated with white light (A) without a filter, and ultraviolet LED light (B) through a blue light cutting filter (<490 nm). (C) A reflectance and fluorescence light spectrum measured from a pale band. -
Why Do We Study Animal Toxins?
ZOOLOGICAL RESEARCH Why do we study animal toxins? Yun ZHANG* Key Laboratory of Animal Models and Human Disease Mechanisms of The Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming Yunnan 650223, China ABSTRACT Biological roles of venoms........................................................................(187) Predation.....................................................................................................(187) Defense .......................................................................................................(187) Venom (toxins) is an important trait evolved along Competition ................................................................................................(188) the evolutionary tree of animals. Our knowledges on Antimicrobial defense ................................................................................(188) venoms, such as their origins and loss, the biological Communication ..........................................................................................(188) relevance and the coevolutionary patterns with other Venom loss..................................................................................................(188) Toxins in animal venoms..........................................................................(188) organisms are greatly helpful in understanding many Selection pressures and animal toxins........................................................(188) fundamental biological questions, i.e., -
Marine Reptiles Arne R
Virginia Commonwealth University VCU Scholars Compass Study of Biological Complexity Publications Center for the Study of Biological Complexity 2011 Marine Reptiles Arne R. Rasmessen The Royal Danish Academy of Fine Arts John D. Murphy Field Museum of Natural History Medy Ompi Sam Ratulangi University J. Whitfield iG bbons University of Georgia Peter Uetz Virginia Commonwealth University, [email protected] Follow this and additional works at: http://scholarscompass.vcu.edu/csbc_pubs Part of the Life Sciences Commons Copyright: © 2011 Rasmussen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Downloaded from http://scholarscompass.vcu.edu/csbc_pubs/20 This Article is brought to you for free and open access by the Center for the Study of Biological Complexity at VCU Scholars Compass. It has been accepted for inclusion in Study of Biological Complexity Publications by an authorized administrator of VCU Scholars Compass. For more information, please contact [email protected]. Review Marine Reptiles Arne Redsted Rasmussen1, John C. Murphy2, Medy Ompi3, J. Whitfield Gibbons4, Peter Uetz5* 1 School of Conservation, The Royal Danish Academy of Fine Arts, Copenhagen, Denmark, 2 Division of Amphibians and Reptiles, Field Museum of Natural History, Chicago, Illinois, United States of America, 3 Marine Biology Laboratory, Faculty of Fisheries and Marine Sciences, Sam Ratulangi University, Manado, North Sulawesi, Indonesia, 4 Savannah River Ecology Lab, University of Georgia, Aiken, South Carolina, United States of America, 5 Center for the Study of Biological Complexity, Virginia Commonwealth University, Richmond, Virginia, United States of America Of the more than 12,000 species and subspecies of extant Caribbean, although some species occasionally travel as far north reptiles, about 100 have re-entered the ocean. -
An Investigation of the Evolution of Australian Elapid Snake Venoms
toxins Article Rapid Radiations and the Race to Redundancy: An Investigation of the Evolution of Australian Elapid Snake Venoms Timothy N. W. Jackson 1, Ivan Koludarov 1, Syed A. Ali 1,2, James Dobson 1, Christina N. Zdenek 1, Daniel Dashevsky 1, Bianca op den Brouw 1, Paul P. Masci 3, Amanda Nouwens 4, Peter Josh 4, Jonathan Goldenberg 1, Vittoria Cipriani 1, Chris Hay 1, Iwan Hendrikx 1, Nathan Dunstan 5, Luke Allen 5 and Bryan G. Fry 1,* 1 Venom Evolution Lab, School of Biological Sciences, University of Queensland, St Lucia, QLD 4072, Australia; [email protected] (T.N.W.J.); [email protected] (I.K.); [email protected] (S.A.A.); [email protected] (J.D.); [email protected] (C.N.Z.); [email protected] (D.D.); [email protected] (B.o.d.B.); [email protected] (J.G.); [email protected] (V.C.); [email protected] (C.H.); [email protected] (I.H.) 2 HEJ Research Institute of Chemistry, International Centre for Chemical and Biological Sciences (ICCBS), University of Karachi, Karachi 75270, Pakistan 3 Princess Alexandra Hospital, Translational Research Institute, University of Queensland, St Lucia, QLD 4072, Australia; [email protected] 4 School of Chemistry and Molecular Biosciences, University of Queensland, St Lucia, QLD 4072, Australia; [email protected] (A.N.); [email protected] (P.J.) 5 Venom Supplies, Tanunda, South Australia 5352, Australia; [email protected] (N.D.); [email protected] (L.A.) * Correspondence: [email protected]; Tel.: +61-4-0019-3182 Academic Editor: Nicholas R. -
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.