Northern Rubber Boa (Charina Bottae) Predicted Suitable Habitat Modeling
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Rubber Boas in Radium Hot Springs: Habitat, Inventory, and Management Strategies
Rubber Boas in Radium Hot Springs: Habitat, Inventory, and Management Strategies ROBERT C. ST. CLAIR1 AND ALAN DIBB2 19809 92 Avenue, Edmonton, AB, T6E 2V4, Canada, email [email protected] 2Parks Canada, Box 220, Radium Hot Springs, BC, V0A 1M0, Canada Abstract: Radium Hot Springs in Kootenay National Park, British Columbia is home to a population of rubber boas (Charina bottae). This population is of ecological and physiological interest because the hot springs seem to be a thermal resource for the boas, which are near the northern limit of their range. This population also presents a dilemma to park management because the site is a major tourist destination and provides habitat for the rubber boa, which is listed as a species of Special Concern by the Committee on the Status of Endangered Wildlife in Canada (COSEWIC). An additional dilemma is that restoration projects, such as prescribed logging and burning, may increase available habitat for the species but kill individual snakes. Successful management of the population depends on monitoring the population, assessing the impacts of restoration strategies, and mapping both summer and winter habitat. Hibernation sites may be discovered only by using radiotelemetry to follow individuals. Key Words: rubber boa, Charina bottae, Radium Hot Springs, hot springs, snakes, habitat, restoration, Kootenay National Park, British Columbia Introduction The presence of rubber boas (Charina bottae) at Radium Hot Springs in Kootenay National Park, British Columbia (B.C.) presents some unusual challenges for wildlife managers because the site is a popular tourist resort and provides habitat for the species, which is listed as a species of Special Concern by the Committee on the Status of Endangered Wildlife in Canada (COSEWIC 2004). -
Review of Species Selected at SRG 45 Following Working Group Recommendations on Reptiles and One Scorpion from Benin, Ghana and Togo
Review of species selected at SRG 45 following working group recommendations on reptiles and one scorpion from Benin, Ghana and Togo (Version edited for public release) A report to the European Commission Directorate General E - Environment ENV.E.2. – Environmental Agreements and Trade by the United Nations Environment Programme World Conservation Monitoring Centre November, 2008 UNEP World Conservation Monitoring Centre 219 Huntingdon Road Cambridge CB3 0DL CITATION United Kingdom UNEP-WCMC (2008). Review of species selected at SRG 45 following working group recommendations on reptiles Tel: +44 (0) 1223 277314 and one scorpion from Benin, Ghana and Togo. A Report Fax: +44 (0) 1223 277136 to the European Commission. UNEP-WCMC, Cambridge. Email: [email protected] Website: www.unep-wcmc.org PREPARED FOR ABOUT UNEP-WORLD CONSERVATION The European Commission, Brussels, Belgium MONITORING CENTRE The UNEP World Conservation Monitoring Centre DISCLAIMER (UNEP-WCMC), based in Cambridge, UK, is the The contents of this report do not necessarily reflect specialist biodiversity information and assessment the views or policies of UNEP or contributory centre of the United Nations Environment organisations. The designations employed and the Programme (UNEP), run cooperatively with WCMC presentations do not imply the expressions of any 2000, a UK charity. The Centre's mission is to opinion whatsoever on the part of UNEP, the evaluate and highlight the many values of European Commission or contributory organisations biodiversity and put authoritative biodiversity concerning the legal status of any country, territory, knowledge at the centre of decision-making. city or area or its authority, or concerning the Through the analysis and synthesis of global delimitation of its frontiers or boundaries. -
Calabaria and the Phytogeny of Erycine Snakes
<nological Journal of the Linnean Socieb (1993), 107: 293-351. With 19 figures Calabaria and the phylogeny of erycine snakes ARNOLD G. KLUGE Museum of <oolog~ and Department of Biology, University of Michigan, Ann Arbor, Mr 48109 U.S.A. Receiued October 1991, revised manuscript accepted Mar I992 Two major subgroups of erycine snakes, designated Charina and Eyx, are delimited with a cladistic analysis of 75 morphological characters. The hypotheses of species relationships within the two clades are (reinhardtii (bottae, triuirgata) ) and (colubrinus, conicus, elegans, jayakari, muellen’, somalicus (miliaris (tataricus (iaculus, johnii)))),respectively. This pattern of grouping obtains without assuming multistate character additivity. At least 16 synapomorphies indicate that reinhardtii is an erycine and that it is the sister lineage of the (bottae, friuirgata) cladr. Calabaria and Lichanura are synonymized with Charina for reasons of taxonomic efficiency, and to emphasize the New-Old World geographic distribution of the three species in that assemblage. Further resolution of E’yx species relationships is required before Congylophis (type species conicus) can be recognized. ADDITIONAL KEY WORDS:--Biogeography - Cladistics - erycines - fossils - taxonomy CONI‘EN’I’S Introduction ................... 293 Erycine terminal taxa and nomenclature ............ 296 Fossils .................... 301 Methods and materials ................ 302 Eryrine phylogeny ................. 306 Character descriptions ............... 306 Other variation ................ -
Class: Amphibia Amphibians Order
CLASS: AMPHIBIA AMPHIBIANS ANNIELLIDAE (Legless Lizards & Allies) CLASS: AMPHIBIA AMPHIBIANS Anniella (Legless Lizards) ORDER: ANURA FROGS AND TOADS ___Silvery Legless Lizard .......................... DS,RI,UR – uD ORDER: ANURA FROGS AND TOADS BUFONIDAE (True Toad Family) BUFONIDAE (True Toad Family) ___Southern Alligator Lizard ............................ RI,DE – fD Bufo (True Toads) Suborder: SERPENTES SNAKES Bufo (True Toads) ___California (Western) Toad.............. AQ,DS,RI,UR – cN ___California (Western) Toad ............. AQ,DS,RI,UR – cN ANNIELLIDAE (Legless Lizards & Allies) Anniella ___Red-spotted Toad ...................................... AQ,DS - cN BOIDAE (Boas & Pythons) ___Red-spotted Toad ...................................... AQ,DS - cN (Legless Lizards) Charina (Rosy & Rubber Boas) ___Silvery Legless Lizard .......................... DS,RI,UR – uD HYLIDAE (Chorus Frog and Treefrog Family) ___Rosy Boa ............................................ DS,CH,RO – fN HYLIDAE (Chorus Frog and Treefrog Family) Pseudacris (Chorus Frogs) Pseudacris (Chorus Frogs) Suborder: SERPENTES SNAKES ___California Chorus Frog ............ AQ,DS,RI,DE,RO – cN COLUBRIDAE (Colubrid Snakes) ___California Chorus Frog ............ AQ,DS,RI,DE,RO – cN ___Pacific Chorus Frog ....................... AQ,DS,RI,DE – cN Arizona (Glossy Snakes) ___Pacific Chorus Frog ........................AQ,DS,RI,DE – cN BOIDAE (Boas & Pythons) ___Glossy Snake ........................................... DS,SA – cN Charina (Rosy & Rubber Boas) RANIDAE (True Frog Family) -
Sensitive Species of Snakes, Frogs, and Salamanders in Southern California Conifer Forest Areas: Status and Management1
Sensitive Species of Snakes, Frogs, and Salamanders in Southern California Conifer Forest Areas: Status and Management1 Glenn R. Stewart2, Mark R. Jennings3, and Robert H. Goodman, Jr.4 Abstract At least 35 species of amphibians and reptiles occur regularly in the conifer forest areas of southern California. Twelve of them have some or all of their populations identified as experiencing some degree of threat. Among the snakes, frogs, and salamanders that we believe need particular attention are the southern rubber boa (Charina bottae umbratica), San Bernardino mountain kingsnake (Lampropeltis zonata parvirubra), San Diego mountain kingsnake (L.z. pulchra), California red-legged frog (Rana aurora draytonii), mountain yellow-legged frog (R. muscosa), San Gabriel Mountain slender salamander (Batrachoseps gabrieli), yellow-blotched salamander (Ensatina eschscholtzii croceater), and large-blotched salamander (E.e. klauberi). To varying degrees, these taxa face threats of habitat degradation and fragmentation, as well as a multitude of other impacts ranging from predation by alien species and human collectors to reduced genetic diversity and chance environmental catastrophes. Except for the recently described San Gabriel Mountain slender salamander, all of these focus taxa are included on Federal and/or State lists of endangered, threatened, or special concern species. Those not federally listed as Endangered or Threatened are listed as Forest Service Region 5 Sensitive Species. All of these taxa also are the subjects of recent and ongoing phylogeographic studies, and they are of continuing interest to biologists studying the evolutionary processes that shape modern species of terrestrial vertebrates. Current information on their taxonomy, distribution, habits and problems is briefly reviewed and management recommendations are made. -
Rubber Boa March 2019
Volume 32/Issue 7 Rubber Boa March 2019 RUBBER BOA INSIDE: Reptiles Heads or Tails? Snakes – Sinister or Sacred? © Tony Iwane CC BY-NC-ND 2.0, Flickr © Natalie McNear CC BY-NC-ND 2.0, Flickr © Natalie McNear CC BY-NC-ND 2.0, Flickr © J. Maughn CC BY-NC-ND 2.0, Flickr © J. Maughn CC BY-NC-ND 2.0, Flickr Rubber Boa o you know that a boa constrictor lives Rubber boas may be found throughout Idaho in Idaho? Many people are surprised from deserts to pine forests. They need water Dto learn that there is a boa constrictor and downed logs or leaf litter nearby. They are found in our state. It is the rubber boa. Its very shy and will burrow in soil and under logs scientific name is Charina bottae (CHA-ree-na and rocks when frightened. They spend most of BOW-tay). Charina means graceful. This is a the day safe in a burrow and come out at dusk fitting name! Rubber boas are graceful as they or during the night. However, they may venture slide and slither over the ground. out of their burrows on a mild, cloudy day to look for food. Sometimes they are seen basking Rubber boas got their name for how they look in the sun, but this is rare. and feel. They have small scales, and the skin is loose on the body. This gives them the look and Rubber boas kill their prey by constriction just feel of rubber. It is sometimes hard to tell which like larger boas. -
Life History Account for Northern Rubber
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group NORTHERN RUBBER BOA Charina bottae Family: BOIDAE Order: SQUAMATA Class: REPTILIA R046 Written by: S. Morey, H. Basey Reviewed by: T. Papenfuss Edited by: R. Duke Updated by: CWHR Program Staff, March 2002 and November 2014 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The northern rubber boa is uncommon to common in suitable habitats. Occurs throughout the Sierra from Ventura Co. north, across the northern part of the state and in the Coast Ranges south nearly to Point Conception. Elevational range is from sea level to 2740 m (9040 ft). Found in a variety of montane forest habitats including red fir, ponderosa pine, hardwood, hardwood-conifer, Douglas fir, redwood, mixed conifer and riparian. Also found in montane chaparral and wet meadow habitats, usually, in the vicinity of streams. A geographically isolated race, once included in this species, was recently updated to the new species C. umbratica (Rodríguez-Robles et al. 2001). It appears to be extremely uncommon and is apparently restricted to the San Bernardino and San Jacinto Mts. (Erwin 1974). SPECIFIC HABITAT REQUIREMENTS Feeding: Food consists primarily of small mammals and lizards (Stebbins 1954, though, it may occasionally take smaller snakes (Linder 1963) and Ensatina (Macey 1983). Cover: The rubber boa is an extremely secretive snake seeking cover in rotting logs, pieces of bark, boards, rocks, and other surface debris. Burrows through loose soil or decaying vegetation. Occasionally climbs. Reproduction: Young are born in loose, well aerated soil, under surface objects, or within rotting logs. Water: No additional information on water requirements. -
THE HUSBANDRY and BREEDING of the ROSY BOA LICHA- By
THE HUSBANDRY AND BREEDING OF THE ROSY BOA LICHA NURA TRIVIRGATA ROSEOFUSCA (COPE, 1861). By: John van der Pols, Gildstraat 190, 3572 EW Utrecht, The Netherlands. Contents: Introduction - Distribution - Systema tics - Etymology - Purchase - Captivity - Care - Mating/Pregnancy - The young - Afterword - References. INTRODUCTION Lichanura trivirgata roseofusca is a relatively small-sized representative of the boid family; adult females reaching a maximum length of only 105 cm (Switak, 1981). This docile species is often active both at night and during the day and usually adjusts quickly to life in captivity, making it a fine pet. DISTRIBUTION Lichanura trivirgata roseofusca can be found in the coastal regions of southern California, in an area stretching down into the northern parts of Baja California (Mexico). Another subspecies, Li chanura trivirgata gracia, shares some parts of Li chanura trivirgata roseofusca's eastern territory; subsequently an intermediate form of the two can be found in the overlapping area (Klauber, 1933). Lichanura trivirgata roseofusca can be found at altitudes of up to 1500 m (Wright & Wright, 1957). SYSTEMATICS The scalation of Lichanura trivirgata roseofusca 98 EE]) Lichanura trivirgata trivirgata EI] Lichanura trivirgata roseofusca flIJlil!IIj. Lichanura trivirgata gracia ~__] Lichanura trivirgata bostici 99 Fig. 1. Lichanura trivirgata roseofusca. Fata: J. van der Pals. Fig. 2. Lichanura trivirgata roseofusca, juv. Fata: J. van der Pals. is as follows: 33-45 dorsal scale rows, 218-232 ventral plates and 39-49 subcaudals. The species Lichanura trivirgata includes four subspecies: Li chanu:ra trivirgata trivirgata (Cope, 1861), Licha nura trivirgata gracia {Klauber, 1931), Lichanura trivirgata roseofusca (Cope, 1868) and Lichanura trivirgata bostici (Ottley, 1978). -
Download Full Article in PDF Format
geodiversitas 2021 43 1 e of lif pal A eo – - e h g e r a p R e t e o d l o u g a l i s C - t – n a M e J e l m a i r o DIRECTEUR DE LA PUBLICATION / PUBLICATION DIRECTOR : Bruno David, Président du Muséum national d’Histoire naturelle RÉDACTEUR EN CHEF / EDITOR-IN-CHIEF : Didier Merle ASSISTANT DE RÉDACTION / ASSISTANT EDITOR : Emmanuel Côtez ([email protected]) MISE EN PAGE / PAGE LAYOUT : Emmanuel Côtez COMITÉ SCIENTIFIQUE / SCIENTIFIC BOARD : Christine Argot (Muséum national d’Histoire naturelle, Paris) Beatrix Azanza (Museo Nacional de Ciencias Naturales, Madrid) Raymond L. Bernor (Howard University, Washington DC) Alain Blieck (chercheur CNRS retraité, Haubourdin) Henning Blom (Uppsala University) Jean Broutin (Sorbonne Université, Paris, retraité) Gaël Clément (Muséum national d’Histoire naturelle, Paris) Ted Daeschler (Academy of Natural Sciences, Philadelphie) Bruno David (Muséum national d’Histoire naturelle, Paris) Gregory D. Edgecombe (The Natural History Museum, Londres) Ursula Göhlich (Natural History Museum Vienna) Jin Meng (American Museum of Natural History, New York) Brigitte Meyer-Berthaud (CIRAD, Montpellier) Zhu Min (Chinese Academy of Sciences, Pékin) Isabelle Rouget (Muséum national d’Histoire naturelle, Paris) Sevket Sen (Muséum national d’Histoire naturelle, Paris, retraité) Stanislav Štamberg (Museum of Eastern Bohemia, Hradec Králové) Paul Taylor (The Natural History Museum, Londres, retraité) COUVERTURE / COVER : Réalisée à partir des Figures de l’article/Made from the Figures of the article. Geodiversitas est -
Sand Boas Photo Gallery
¯ SAND BOAS PHOTO GALLERY ¯¯ ¯ ¯ ¯ ¯ ¯¯ ¯ : : ¯ SAND BOAS PHOTO GALLERY , ,¯ ¯ ¯ , ¯ , ¯ ¯ ¯ ¯ , ¯ ¯ ¯ ,¯ ¯ ¯ ¯ ,¯ ¯ ¯ , ¯ − − ¯ ¯ , ¯ , ¯ ¯ , ¯ ¯ , ¯ ¯ , ¯ ¯ ¯ ï ; ¯ ¯ ¯ , , ¯ ¯ ¯ ¯¯ ¯ ¯ ¯ FACTS ABOUT SAND BOAS ¯ , Boidae ¯ ¯ Erycinae , , ¯ Erycinae ¯ , Charina ¯ Gongylophis ¯ , Eryx , Boidae ¯ ¯ ,¯ ¯ − ¯ Pythonidae ¯ ¯ , , Indian Sand Boa ¯ ¯ , ¯ ¯ ¯ ¯¯ ,¯ ,¯ ¯ ¯ ¯ ;¯ , ¯ ; ¯ ¯ ¯ SAND BOAS PHOTO GALLERY ,¯ ¯ ¯ Sexual Dimorphism ¯ , ¯ ¯ ¯ ¯ ¯ ¯ ¯ ¯ , Ovoviviparous Placenta ï ï , ¯ Yolk Sac ¯ ¯ ¯ , ¯ ¯ ¯ ¯ , ¯ ¯ ¯ Viviparous Calabar ¯ , ¯ ¯ , Boidae ¯ ¯ ¯ , Boa Pythonidae , Charina reinhardtii ¯ Calabaria reinhardtii ¯ ¯ ,¯ ¯ ¯ ¯ , Arabian Sand Boa ¯ ¯ Eryx Saharan Sand Boa , ¯ ¯ ¯ , Gongylophis ¯ Erycinae ¯ ¯ ¯ ¯ TAXONOMY ¯ ¯ Kingdom Animailia Phylum Chordata Class Reptillia ¯ Order Squamata ¯ Suborder Serpentes ¯ Family Boidae Subfamily Erycinae Erycinae ¯ Genus Charina Eryx Gongylophis E. elegans C. bottae E. jaculus G. colubrinus E. jayakari E. johnii E. miliaris G. conicus E. somalicus C. umbratica E. tataricus E. whitakeri G. muelleri -
Protected Wildlife, Holding and Propagating Rules
PROTECTED WILDLIFE, HOLDING AND PROPAGATING RULES CHAPTER 635 DIVISION 44 OREGON FISH AND WILDLIFE COMMISSION JUNE 9, 2016 SALEM, OREGON MARCH 18, 2016 • Revisions from informational briefing • Continue to receive public comment • Provide crossover table of revisions PRESENTATION OUTLINE Background Review Process Overview of Draft Rule Revisions Public Review and Comments BACKGROUND • Clear policy and procedures related to protected wildlife, wildlife holding permits & propagation licenses • Provide clear direction for law enforcement DIVISION 44 REVIEW • 2013 - Interagency Discussions • 2014 /15 - Wildlife Holding Advisory Group Internal Review • January 2016 – Stakeholder Review and Public Comment • March 2016 – Informational Briefing • June 2016 – Proposed Rule Adoption REMOVE CLASSIFICATION OF “NONGAME NON-PROTECTED” All free-ranging wildlife are protected EXCEPT: 1. Regulated take or permit/license or rule 2. Wildlife Holding Permit • Grandfathered animals • Nongame species distributed widely, abundant, secure 3. Propagation License 4. Department approval – Letter of Authorization GRANDFATHERING PROVISION • Black bear • Cougar • Wolf • Bobcat • Raccoon • Skunk • Squirrels • Chipmunk • Nongame Non-protected GRANDFATHERED ANIMAL FACILITIES • Facilities meeting ODFW Enclosure and Caging Standards (Exhibit 1) w/in 1 year • New permits or new acquisitions of captive black bear, cougar, bobcat, wolves • Facilities accredited by Association of Zoos and Aquariums (AZA) DRAFT RULE REVISIONS • System for holding nongame wildlife based on science -
Fauna of Australia 2A
FAUNA of AUSTRALIA 33. FAMILY BOIDAE Harald Ehmann 33. FAMILY BOIDAE Pl. 7.2. Aspidites ramsayi (Boidae): a nocturnal, terrestrial snake, often found sheltering in hollow logs or thick vegetation; occurs in dry areas and deserts across central Australia. [J. Wombey] Pl. 7.3. Chondropython viridis (Boidae): juveniles are often yellow, and coil in the manner shown; (see also Pl 7.4). [H. Cogger] 2 33. FAMILY BOIDAE Pl. 7.4. Chondropython viridis (Bioidae): adults of this species are bright green (see also Pl. 7.3); a nocturnal, arboreal python of the rainforests, north-eastern Cape York. [H. Cogger] Pl. 7.5. Antaresia stimsoni (Boidae): found frequently near rock outcrops, in stone fields, around large trees or other isolated features in sandy deserts; throughout arid central and western parts of Australia. [H. Cogger] 3 33. FAMILY BOIDAE DEFINITION AND GENERAL DESCRIPTION Worldwide the boids include terrestrial, arboreal, burrowing, semi-aquatic and saxicoline species. They are non-venomous, medium-sized or very large snakes. Many of the Australian species are nocturnal and many feed on mammals or birds as adults. Most boids immobilise their prey in tight coilings of the body, and use sustained constriction to kill prey by suffocation (Fig. 33.1). The Boidae are distinguished from other snakes by the presence of vestiges of the pelvis and, usually, hindlimbs which appear as cloacal spurs in live snakes. The supratemporal and quadrate bones are long, resulting in a relatively large mouth. Uniform, large, recurved sharp teeth are present on the dentary, maxilla, palatine, pterygoid. Teeth are present also on the premaxilla of most pythonines.