Sydney's Snakes, Part 3
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Different Environmental Gradients Affect Different Measures of Snake Β-Diversity in the Amazon Rainforests
Different environmental gradients affect different measures of snake β-diversity in the Amazon rainforests Rafael de Fraga1,2,3, Miquéias Ferrão1, Adam J. Stow2, William E. Magnusson4 and Albertina P. Lima4 1 Programa de Pós-Graduação em Ecologia, Instituto Nacional de Pesquisas da Amazônia, Manaus, Amazonas, Brazil 2 Department of Biological Sciences, Macquarie University, Sydney, NSW, Australia 3 Programa de Pós-graduação em Sociedade, Natureza e Desenvolvimento, Universidade Federal do Oeste do Pará, Santarém, Pará, Brazil 4 Coordenação de Biodiversidade, Instituto Nacional de Pesquisas da Amazônia, Manaus, Amazonas, Brazil ABSTRACT Mechanisms generating and maintaining biodiversity at regional scales may be evaluated by quantifying β-diversity along environmental gradients. Differences in assemblages result in biotic complementarities and redundancies among sites, which may be quantified through multi-dimensional approaches incorporating taxonomic β-diversity (TBD), functional β-diversity (FBD) and phylogenetic β-diversity (PBD). Here we test the hypothesis that snake TBD, FBD and PBD are influenced by environmental gradients, independently of geographic distance. The gradients tested are expected to affect snake assemblages indirectly, such as clay content in the soil determining primary production and height above the nearest drainage determining prey availability, or directly, such as percentage of tree cover determining availability of resting and nesting sites, and climate (temperature and precipitation) causing physiological filtering. We sampled snakes in 21 sampling plots, each covering five km2, distributed over 880 km in the central-southern Amazon Basin. We used dissimilarities between sampling sites to quantify TBD, FBD and PBD, Submitted 30 April 2018 which were response variables in multiple-linear-regression and redundancy analysis Accepted 23 August 2018 Published 24 September 2018 models. -
Broad-Headed Snake (Hoplocephalus Bungaroides)', Proceedings of the Royal Zoological Society of New South Wales (1946-7), Pp
Husbandry Guidelines Broad-Headed Snake Hoplocephalus bungaroides Compiler – Charles Morris Western Sydney Institute of TAFE, Richmond Captive Animals Certificate III RUV3020R Lecturers: Graeme Phipps, Jacki Salkeld & Brad Walker 2009 1 Occupational Health and Safety WARNING This Snake is DANGEROUSLY VENOMOUS CAPABLE OF INFLICTING A POTENTIALLY FATAL BITE ALWAYS HAVE A COMPRESSION BANDAGE WITHIN REACH SNAKE BITE TREATMENT: Do NOT wash the wound. Do NOT cut the wound, apply substances to the wound or use a tourniquet. Do NOT remove jeans or shirt as any movement will assist the venom to enter the blood stream. KEEP THE VICTIM STILL. 1. Apply a broad pressure bandage over the bite site as soon as possible. 2. Keep the limb still. The bandage should be as tight as you would bind a sprained ankle. 3. Extend the bandage down to the fingers or toes then up the leg as high as possible. (For a bite on the hand or forearm bind up to the elbow). 4. Apply a splint if possible, to immobilise the limb. 5. Bind it firmly to as much of the limb as possible. (Use a sling for an arm injury). Bring transport to the victim where possible or carry them to transportation. Transport the victim to the nearest hospital. Please Print this page off and put it up on the wall in your snake room. 2 There is some serious occupational health risks involved in keeping venomous snakes. All risk can be eliminated if kept clean and in the correct lockable enclosures with only the risk of handling left in play. -
Ecology and Conservation Biology of the North American Wood Turtle (Glyptemys
Ecology and Conservation Biology of the North American Wood Turtle (Glyptemys insculpta) in the Central Appalachians A dissertation presented to the faculty of the College of Arts and Sciences of Ohio University In partial fulfillment of the requirements for the degree Doctor of Philosophy Steven P. Krichbaum May 2018 © 2018 Steven P. Krichbaum. All Rights Reserved. 2 This dissertation titled Ecology and Conservation Biology of the North American Wood Turtle (Glyptemys insculpta) in the Central Appalachians by STEVEN P. KRICHBAUM has been approved for the Department of Biological Sciences and the College of Arts and Sciences by Willem Roosenburg Professor of Biological Sciences Robert Frank Dean, College of Arts and Sciences 3 Abstract KRICHBAUM, STEVEN P., Ph.D., May 2018, Biological Sciences Ecology and Conservation Biology of the North American Wood Turtle (Glyptemys insculpta) in the Central Appalachians Director of Dissertation: Willem Roosenburg My study presents information on summer use of terrestrial habitat by IUCN “endangered” North American Wood Turtles (Glyptemys insculpta), sampled over four years at two forested montane sites on the southern periphery of the species’ range in the central Appalachians of Virginia (VA) and West Virginia (WV) USA. The two sites differ in topography, stream size, elevation, and forest composition and structure. I obtained location points for individual turtles during the summer, the period of their most extensive terrestrial roaming. Structural, compositional, and topographical habitat features were measured, counted, or characterized on the ground (e.g., number of canopy trees and identification of herbaceous taxa present) at Wood Turtle locations as well as at paired random points located 23-300m away from each particular turtle location. -
Approved Conservation Advice for Hoplocephalus Bungaroides (Broad-Headed Snake)
This Conservation Advice was approved by the Delegate of the Minister on 11 April 2014 Approved Conservation Advice for Hoplocephalus bungaroides (broad-headed snake) (s266B of the Environment Protection and Biodiversity Conservation Act 1999) This Conservation Advice has been developed based on the best available information at the time this Conservation Advice was approved; this includes existing and draft plans, records or management prescriptions for this species. Description Hoplocephalus bungaroides (broad-headed snake), family Elapidae, is black above with yellow spots forming narrow, irregular cross-bands. Other yellow scales may link these cross-bands laterally to form a straight or zigzagged stripe along the body. These cross- bands help distinguish it from the similar-looking juvenile diamond python (Morelia spilota). Its head is flattened on top and is distinct from the body. The belly is grey or greyish-black. The average length is about 60 cm, with a maximum of around 150 cm. Birth occurs in January to March (OEH, 2012). The species is active at dusk (Wells, 1981, cited in NSW NPWS, 1999). Conservation Status The broad-headed snake is listed as vulnerable under the name Hoplocephalus bungaroides Broad-headed Snake. This species is eligible for listing as vulnerable under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act) as, prior to the commencement of the EPBC Act, it was listed as vulnerable under Schedule 1 of the Endangered Species Protection Act 1992 (Cwlth). The species is also listed as endangered under the Threatened Species Conservation Act 1995 (New South Wales) and vulnerable under the IUCN Red List of Threatened Species 2013.1 (Australasian Reptile & Amphibian Specialist Group, 1996). -
Phylogenetic Relationships of Terrestrial Australo-Papuan Elapid Snakes (Subfamily Hydrophiinae) Based on Cytochrome B and 16S Rrna Sequences J
MOLECULAR PHYLOGENETICS AND EVOLUTION Vol. 10, No. 1, August, pp. 67–81, 1998 ARTICLE NO. FY970471 Phylogenetic Relationships of Terrestrial Australo-Papuan Elapid Snakes (Subfamily Hydrophiinae) Based on Cytochrome b and 16S rRNA Sequences J. Scott Keogh,*,†,1 Richard Shine,* and Steve Donnellan† *School of Biological Sciences A08, University of Sydney, Sydney, New South Wales 2006, Australia; and †Evolutionary Biology Unit, South Australian Museum, North Terrace, Adelaide, South Australia 5000, Australia Received April 24, 1997; revised September 4, 1997 quence data support many of the conclusions reached Phylogenetic relationships among the venomous Aus- by earlier studies using other types of data, but addi- tralo-Papuan elapid snake radiation remain poorly tional information will be needed before the phylog- resolved, despite the application of diverse data sets. eny of the Australian elapids can be fully resolved. To examine phylogenetic relationships among this 1998 Academic Press enigmatic group, portions of the cytochrome b and 16S Key Words: mitochondrial DNA; cytochrome b; 16S rRNA mitochondrial DNA genes were sequenced from rRNA; reptile; snake; elapid; sea snake; Australia; New 19 of the 20 terrestrial Australian genera and 6 of the 7 Guinea; Pacific; Asia; biogeography. terrestrial Melanesian genera, plus a sea krait (Lati- cauda) and a true sea snake (Hydrelaps). These data clarify several significant issues in elapid phylogeny. First, Melanesian elapids form sister groups to Austra- INTRODUCTION lian species, indicating that the ancestors of the Austra- lian radiation came via Asia, rather than representing The diverse, cosmopolitan, and medically important a relict Gondwanan radiation. Second, the two major elapid snakes are a monophyletic clade of approxi- groups of sea snakes (sea kraits and true sea snakes) mately 300 species and 61 genera (Golay et al., 1993) represent independent invasions of the marine envi- primarily defined by their unique venom delivery sys- ronment. -
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. -
Frogs & Reptiles NE Vic 2018 Online
Reptiles and Frogs of North East Victoria An Identication and Conservation Guide Victorian Conservation Status (DELWP Advisory List) cr critically endangered en endangered Reptiles & Frogs vu vulnerable nt near threatened dd data deficient L Listed under the Flora and Fauna Guarantee Act (FFG, 1988) Size: of North East Victoria Lizards, Dragons & Skinks: Snout-vent length (cm) Snakes, Goannas: Total length (cm) An Identification and Conservation Guide Lowland Copperhead Highland Copperhead Carpet Python Gray's Blind Snake Nobbi Dragon Bearded Dragon Ragged Snake-eyed Skink Large Striped Skink Frogs: Snout-vent length male - M (mm) Snout-vent length female - F (mm) Austrelaps superbus 170 (NC) Austrelaps ramsayi 115 (PR) Morelia spilota metcalfei – en L 240 (DM) Ramphotyphlops nigrescens 38 (PR) Diporiphora nobbi 8.4 (PR) Pogona barbata – vu 25 (DM) Cryptoblepharus pannosus Snout-Vent 3.5 (DM) Ctenotus robustus Snout-Vent 12 (DM) Guide to symbols Venomous Lifeform F Fossorial (burrows underground) T Terrestrial Reptiles & Frogs SA Semi Arboreal R Rock-dwelling Habitat Type Alpine Bog Montane Forests Alpine Grassland/Woodland Lowland Grassland/Woodland White-lipped Snake Tiger Snake Woodland Blind Snake Olive Legless Lizard Mountain Dragon Marbled Gecko Copper-tailed Skink Alpine She-oak Skink Drysdalia coronoides 40 (PR) Notechis scutatus 200 (NC) Ramphotyphlops proximus – nt 50 (DM) Delma inornata 13 (DM) Rankinia diemensis Snout-Vent 7.5 (NC) Christinus marmoratus Snout-Vent 7 (PR) Ctenotus taeniolatus Snout-Vent 8 (DM) Cyclodomorphus praealtus -
A New Species of the Australian Bandy Bandy Vermicella Gray, 1841 (Serpentes: Elapidae) from North-West Australia
Australasian Journal of Herpetology 39 Australasian Journal of Herpetology 47:39-41. Published 9 July 2020. ISSN 1836-5698 (Print) ISSN 1836-5779 (Online) A new species of the Australian Bandy Bandy Vermicella Gray, 1841 (Serpentes: Elapidae) from north-west Australia. LSIDURN:LSID:ZOOBANK.ORG:PUB:CBC854A2-50FE-4E74-AB62-7FF940C9C506 RAYMOND T. HOSER LSID urn:lsid:zoobank.org:author:F9D74EB5-CFB5-49A0-8C7C-9F993B8504AE 488 Park Road, Park Orchards, Victoria, 3134, Australia. Phone: +61 3 9812 3322 Fax: 9812 3355 E-mail: snakeman (at) snakeman.com.au Received 3 April 2020, Accepted 14 April 2020, Published 9 July 2020. ABSTRACT Hoser in 2019 reviewed the wide-ranging Bandy Bandy group of snakes, Vermicella Gray, 1841, as defined by Cogger (2014). After inspection of specimens from all parts of their range in continental Australia, a greater diversity than indicated by the then current taxonomy was found. As a result of that paper, five species and three subspecies were formally recognized. This paper formally names a sixth valid species for the genus. Vermicella sloppi sp. nov. has until now been treated as a northern population of V. snelli Storr (1967) as defined by Storr in that paper. However genetic divergence across the known biogeographical barrier of the Fortescue River Valley combined with the morphological divergence of the population, is a compelling argument for recognition of this population as a separate species. The new species is formally named Vermicella sloppi sp. nov.in accordance with the rules of the International Code of Zoological Nomenclature (Ride et al. 1999). Keywords: Taxonomy; nomenclature; snakes; Elapidae; Australia; Western Australia; New Vermicella; snelli; new species; sloppi. -
Population Ecology of a Cryptic Arboreal Snake (Hoplocephalus Bitorquatus)
CSIRO PUBLISHING Australian Journal of Zoology https://doi.org/10.1071/ZO18009 Population ecology of a cryptic arboreal snake (Hoplocephalus bitorquatus) Michael B. Shelton A,C, Ross L. Goldingay A and Stephen S. Phillips B ASchool of Environment, Science and Engineering, Southern Cross University, Lismore, NSW 2480, Australia. BBiolink Ecological Consultants, 9 Marshall Street, Uki, NSW 2484, Australia. CCorresponding author. Email: [email protected] Abstract. Biologists have traditionally been reluctant to study arboreal snakes due to low rates of capture. Overlooking such taxa can mislead interpretations of population trends for data-deficient species. We used regularly spaced transect searches and standard capture–mark–recapture techniques to describe population structure, growth rates, survival and capture probability in a population of the pale-headed snake (Hoplocephalus bitorquatus) in southern Queensland. We obtained data from 194 captures of 113 individual snakes between 2009 and 2015. Using the Cormack–Jolly–Seber method, we estimated apparent annual survival in subadult snakes at 0.23 Æ 0.01 (s.e.) and 0.81 Æ 0.08 for adults. Capture probability was estimated at 0.16 Æ 0.14 per session in subadult snakes and 0.33 Æ 0.06 for adults. Within the red gum forests of our study site, we estimate pale-headed snake density at ~13 Æ 7ha–1. Using von Bertalanffy growth modelling, we predict that snakes reach sexual maturity after about four years and may live for up to 20. Our results suggest that the species is a ‘k’ strategist, characterised by slow maturation and low fecundity. These traits suggest that populations will recover slowly following decline, exacerbating the risk of local extinction. -
Fauna of Australia 2A
FAUNA of AUSTRALIA 23. GENERAL DESCRIPTION AND DEFINITION OF THE SQUAMATA Harold G. Cogger 23. GENERAL DESCRIPTION AND DEFINITION OF THE SQUAMATA The Squamata are members of the diapsid subclass Lepidosauromorpha, a group whose only living descendants are the lizards, amphisbaenians, snakes and tuataras. The lizards, amphisbaenians and snakes together constitute the Order Squamata (or Superorder Squamata, according to Estes 1983). Because the Squamata include approximately 95% of living reptiles, the phylogenetic position of this group within the Lepidosauromorpha, its component taxa, and their diagnostic features, have been the subject of numerous reviews (Estes & Pregill 1988; Kluge 1989). The three suborders of the Squamata include the Sauria (lizards) and the Serpentes (snakes), which are represented in Australia by diverse faunas of nearly 500 species, and 250 species, respectively. The third suborder, the Amphisbaenia, comprises a small group of worm lizards and related species which do not occur in Australia. The earliest known squamate fossils date from the late Permian and early Triassic, approximately 230 million years ago. These early fossils were already clearly lizard-like in their preserved features. Carroll (1988a) points out that lizards (the first squamates) do not appear to have originated as a result of ‘...a significant shift in behavioral patterns or the evolution of major new structural elements, but rather may be seen as resulting from the gradual accumulation of improvements in feeding, locomotion, and sensory apparatus.’ Carroll (1988b) includes among these changes the emargination of the lower temporal fenestra and the development of a joint between the upper end of the quadrate and the squamosal. -
Exotic Snake Bite: a Challenge for the Scandinavian Anesthesiologist?
Exotic snake bite: a challenge for the Scandinavian anesthesiologist? Chew, Michelle; Guttormsen, A B; Metzsch, Carsten; Jahr, John Published in: Acta Anaesthesiologica Scandinavica DOI: 10.1034/j.1399-6576.2003.00049.x 2003 Link to publication Citation for published version (APA): Chew, M., Guttormsen, A. B., Metzsch, C., & Jahr, J. (2003). Exotic snake bite: a challenge for the Scandinavian anesthesiologist? Acta Anaesthesiologica Scandinavica, 47(2), 226-229. https://doi.org/10.1034/j.1399- 6576.2003.00049.x Total number of authors: 4 General rights Unless other specific re-use rights are stated the following general rights apply: 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. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal Read more about Creative commons licenses: https://creativecommons.org/licenses/ Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. LUND UNIVERSITY PO Box 117 221 00 Lund +46 46-222 00 00 Acta Anaesthesiol Scand 2003; 47: 226Ð229 Copyright # Acta Anaesthesiol Scand 2003 Printed in Denmark. -
Tan Choo Hock Thesis Submitted in Fulfi
TOXINOLOGICAL CHARACTERIZATIONS OF THE VENOM OF HUMP-NOSED PIT VIPER (HYPNALE HYPNALE) TAN CHOO HOCK THESIS SUBMITTED IN FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY FACULTY OF MEDICINE UNIVERSITY OF MALAYA KUALA LUMPUR 2013 Abstract Hump-nosed pit viper (Hypnale hypnale) is a medically important snake in Sri Lanka and Western Ghats of India. Envenomation by this snake still lacks effective antivenom clinically. The species is also often misidentified, resulting in inappropriate treatment. The median lethal dose (LD50) of H. hypnale venom varies from 0.9 µg/g intravenously to 13.7 µg/g intramuscularly in mice. The venom shows procoagulant, hemorrhagic, necrotic, and various enzymatic activities including those of proteases, phospholipases A2 and L-amino acid oxidases which have been partially purified. The monovalent Malayan pit viper antivenom and Hemato polyvalent antivenom (HPA) from Thailand effectively cross-neutralized the venom’s lethality in vitro (median effective dose, ED50 = 0.89 and 1.52 mg venom/mL antivenom, respectively) and in vivo in mice, besides the procoagulant, hemorrhagic and necrotic effects. HPA also prevented acute kidney injury in mice following experimental envenomation. Therefore, HPA may be beneficial in the treatment of H. hypnale envenomation. H. hypnale-specific antiserum and IgG, produced from immunization in rabbits, effectively neutralized the venom’s lethality and various toxicities, indicating the feasibility to produce an effective specific antivenom with a common immunization regime. On indirect ELISA, the IgG cross-reacted extensively with Asiatic crotalid venoms, particularly that of Calloselasma rhodostoma (73.6%), suggesting that the two phylogenically related snakes share similar venoms antigenic properties.