Standard Common and Current Scientific Names for North American Amphibians, Turtles, Reptiles & Crocodilians
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(2007) a Photographic Field Guide to the Reptiles and Amphibians Of
A Photographic Field Guide to the Reptiles and Amphibians of Dominica, West Indies Kristen Alexander Texas A&M University Dominica Study Abroad 2007 Dr. James Woolley Dr. Robert Wharton Abstract: A photographic reference is provided to the 21 reptiles and 4 amphibians reported from the island of Dominica. Descriptions and distribution data are provided for each species observed during this study. For those species that were not captured, a brief description compiled from various sources is included. Introduction: The island of Dominica is located in the Lesser Antilles and is one of the largest Eastern Caribbean islands at 45 km long and 16 km at its widest point (Malhotra and Thorpe, 1999). It is very mountainous which results in extremely varied distribution of habitats on the island ranging from elfin forest in the highest elevations, to rainforest in the mountains, to dry forest near the coast. The greatest density of reptiles is known to occur in these dry coastal areas (Evans and James, 1997). Dominica is home to 4 amphibian species and 21 (previously 20) reptile species. Five of these are endemic to the Lesser Antilles and 4 are endemic to the island of Dominica itself (Evans and James, 1997). The addition of Anolis cristatellus to species lists of Dominica has made many guides and species lists outdated. Evans and James (1997) provides a brief description of many of the species and their habitats, but this booklet is inadequate for easy, accurate identification. Previous student projects have documented the reptiles and amphibians of Dominica (Quick, 2001), but there is no good source for students to refer to for identification of these species. -
REPTILIA: SQUAMATA: TEIIDAE AMEIVA CORVINA Ameiva Corvina
REPTILIA: SQUAMATA: TEIIDAE AMEIVACORVINA Catalogue of American Amphibians and Reptiles. Shew, J.J., E.J. Censky, and R. Powell. 2002. Ameiva corvina. Ameiva corvina Cope Sombrero Island Ameiva Ameiva corvina Cope 186 1:3 12. Type locality, "island of Som- brero." Lectotype (designated by Censky and Paulson 1992), Academy of Natural Sciences of Philadelphia (ANSP) 9 116, an adult male, collected by J.B. Hansen, date of collection not known (examined by EJC). See Remarks. CONTENT. No subspecies are recognized. DEFINITION. Ameiva corvina is a moderately sized mem- ber of the genus Ameiva (maximum SVL of males = 133 rnm, of females = 87 mm;Censky and Paulson 1992). Granular scales around the body number 139-156 (r = 147.7 f 2.4, N = 16), ventral scales 32-37 (7 = 34.1 + 0.3, N = 16), fourth toe subdigital lamellae 34-41 (F = 38.1 + 0.5, N = IS), fifteenth caudal verticil 29-38 (r = 33.3 0.6, N = 17), and femoral I I I + MAP. The arrow indicates Sombrero Island, the type locality and en- pores (both legs) 5M3(r = 57.3 0.8, N = 16)(Censky and + tire range of An~eivacorvina. Paulson 1992). See Remarks. Dorsal and lateral coloration is very dark brown to slate black and usually patternless (one individual, MCZ 6141, has a trace of a pattern with faded spots on the posterior third of the dor- sum and some balck blotches on the side of the neck). Brown color often is more distinct on the heads of males. The venter is very dark blue-gray. -
Predation on Ameiva Ameiva (Squamata: Teiidae) by Ardea Alba (Pelecaniformes: Ardeidae) in the Southwestern Brazilian Amazon
Herpetology Notes, volume 14: 1073-1075 (2021) (published online on 10 August 2021) Predation on Ameiva ameiva (Squamata: Teiidae) by Ardea alba (Pelecaniformes: Ardeidae) in the southwestern Brazilian Amazon Raul A. Pommer-Barbosa1,*, Alisson M. Albino2, Jessica F.T. Reis3, and Saara N. Fialho4 Lizards and frogs are eaten by a wide range of wetlands, being found mainly in lakes, wetlands, predators and are a food source for many bird species flooded areas, rivers, dams, mangroves, swamps, in neotropical forests (Poulin et al., 2001). However, and the shallow waters of salt lakes. It is a species predation events are poorly observed in nature and of diurnal feeding habits, but its activity peak occurs hardly documented (e.g., Malkmus, 2000; Aguiar and either at dawn or dusk. This characteristic changes Di-Bernardo, 2004; Silva et al., 2021). Such records in coastal environments, where its feeding habit is are certainly very rare for the teiid lizard Ameiva linked to the tides (McCrimmon et al., 2020). Its diet ameiva (Linnaeus, 1758) (Maffei et al., 2007). is varied and may include amphibians, snakes, insects, Found in most parts of Brazil, A. ameiva is commonly fish, aquatic larvae, mollusks, small crustaceans, small known as Amazon Racerunner or Giant Ameiva, and birds, small mammals, and lizards (Martínez-Vilalta, it has one of the widest geographical distributions 1992; Miranda and Collazo, 1997; Figueroa and among neotropical lizards. It occurs in open areas all Corales Stappung, 2003; Kushlan and Hancock 2005). over South America, the Galapagos Islands (Vanzolini We here report a predation event on the Ameiva ameiva et al., 1980), Panama, and several Caribbean islands by Ardea alba in the southwestern Brazilian Amazon. -
ADOT Herbicide Treatment Program on Bureau of Land Management Lands in Arizona
October 2015 BLM DOI-BLM-AZ-0000-2013-0001-EA ADOT Herbicide Treatment Program on Bureau of Land Management Lands in Arizona Final Environmental Assessment Bureau of Land Management Environmental Assessment and Section 4(f) Evaluation ADOT Herbicide Treatment Program on Bureau of Land Management Lands in Arizona DOI-BLM-AZ-0000-2013-0001-EA Bureau of Land Management Arizona State Office One North Central Avenue, Suite 800 Phoenix, Arizona 85004-4427 October 2015 TABLE OF CONTENTS Table of Contents ............................................................................................................................. i List of Tables ................................................................................................................................... iii List of Figures .................................................................................................................................. iii Acronym List ................................................................................................................................... iv Section 1 – Proposed Action, Purpose and Need, and Background Information ........................... 1 1.1 Introduction...................................................................................................................... 1 1.2 Proposed Action Overview ............................................................................................... 3 1.3 Purpose and Need for Action .......................................................................................... -
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Lamoreux, J. F., McKnight, M. W., and R. Cabrera Hernandez (2015). Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca. Gland, Switzerland: IUCN. xxiv + 320pp. ISBN: 978-2-8317-1717-3 DOI: 10.2305/IUCN.CH.2015.SSC-OP.53.en Cover photographs: Totontepec landscape; new Plectrohyla species, Ixalotriton niger, Concepción Pápalo, Thorius minutissimus, Craugastor pozo (panels, left to right) Back cover photograph: Collecting in Chamula, Chiapas Photo credits: The cover photographs were taken by the authors under grant agreements with the two main project funders: NGS and CEPF. -
An Annotated Type Catalogue of the Dragon Lizards (Reptilia: Squamata: Agamidae) in the Collection of the Western Australian Museum Ryan J
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 34 115–132 (2019) DOI: 10.18195/issn.0312-3162.34(2).2019.115-132 An annotated type catalogue of the dragon lizards (Reptilia: Squamata: Agamidae) in the collection of the Western Australian Museum Ryan J. Ellis Department of Terrestrial Zoology, Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. Biologic Environmental Survey, 24–26 Wickham St, East Perth, Western Australia 6004, Australia. Email: [email protected] ABSTRACT – The Western Australian Museum holds a vast collection of specimens representing a large portion of the 106 currently recognised taxa of dragon lizards (family Agamidae) known to occur across Australia. While the museum’s collection is dominated by Western Australian species, it also contains a selection of specimens from localities in other Australian states and a small selection from outside of Australia. Currently the museum’s collection contains 18,914 agamid specimens representing 89 of the 106 currently recognised taxa from across Australia and 27 from outside of Australia. This includes 824 type specimens representing 45 currently recognised taxa and three synonymised taxa, comprising 43 holotypes, three syntypes and 779 paratypes. Of the paratypes, a total of 43 specimens have been gifted to other collections, disposed or could not be located and are considered lost. An annotated catalogue is provided for all agamid type material currently and previously maintained in the herpetological collection of the Western Australian Museum. KEYWORDS: type specimens, holotype, syntype, paratype, dragon lizard, nomenclature. INTRODUCTION Australia was named by John Edward Gray in 1825, The Agamidae, commonly referred to as dragon Clamydosaurus kingii Gray, 1825 [now Chlamydosaurus lizards, comprises over 480 taxa worldwide, occurring kingii (Gray, 1825)]. -
Site-Specific Environmental Assessment
Environmental Assessment Rangeland Grasshopper and Mormon Cricket Suppression Program ARIZONA EA Number: AZ-20-01 Site-Specific Graham and Gila County portion within the San Carlos Apache Reservation; Mohave County Hualapai Reservation; Cochise County portion of Coronado National Forest – Winchester Mountains Prepared by: Animal and Plant Health Inspection Service 3640 East Wier Ave. Phoenix, Arizona 85040 May 6, 2020 1 Table of Contents I. Need for Proposed Action ...................................................................................................... 4 A. Purpose and Need Statement .............................................................................................. 4 B. Background Discussion ...................................................................................................... 5 C. About This Process ............................................................................................................. 7 II. Alternatives ............................................................................................................................ 7 A. No Action Alternative ......................................................................................................... 8 B. Insecticide Applications at Conventional Rates or Reduced Agent Area Treatments with Adaptive Management Strategy (Preferred Alternative) .......................................................................... 8 C. Experimental Treatments Alternative .............................................................................. -
Biological Conservation 228 (2018) 310–318
Biological Conservation 228 (2018) 310–318 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Multi-scale effects of land cover and urbanization on the habitat suitability of an endangered toad T ⁎ Michael L. Tregliaa, , Adam C. Landonb,c,1, Robert N. Fisherd, Gerard Kyleb, Lee A. Fitzgeralda a Department of Wildlife and Fisheries Sciences, Biodiversity Research and Teaching Collections, Applied Biodiversity Science Program, Texas A&M University, College Station, TX 77843-2258, USA b Human Dimensions of Natural Resources Lab, Department of Recreation, Parks, and Tourism Sciences, Texas A&M University, College Station, TX 77843-2261, USA c Water Management and Hydrological Science Program, Texas A&M University, College Station, TX 77843-3408, USA d U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, San Diego, CA, USA ARTICLE INFO ABSTRACT Keywords: Habitat degradation, entwined with land cover change, is a major driver of biodiversity loss. Effects of land cover Watersheds change on species can be direct (when habitat is converted to alternative land cover types) or indirect (when Structural equation model land outside of the species habitat is altered). Hydrologic and ecological connections between terrestrial and California aquatic systems are well understood, exemplifying how spatially disparate land cover conditions may influence Arroyo toad aquatic habitats, but are rarely examined. We sought to quantify relative effects of land cover at two different but Anaxyrus californicus interacting scales on habitat suitability for the endangered arroyo toad (Anaxyrus californicus). Based on an Anthropogenic development ff Riparian areas existing distribution model for the arroyo toad and available land cover data, we estimated e ects of land cover along streams and within entire watersheds on habitat suitability using structural equation modeling. -
Arroyo Toad (Anaxyrus Californicus) Life History, Population Status, Population
Arroyo Toad (Anaxyrus californicus) Life History, Population Status, Population Threats, and Habitat Assessment of Conditions at Fort Hunter Liggett, Monterey County, California A Thesis presented to the Faculty of California Polytechnic State University, San Luis Obispo In Partial Fulfillment of the Requirements for the Degree Master of Science in Biology by Jacquelyn Petrasich Hancock December 2009 © 2009 Jacquelyn Petrasich Hancock ALL RIGHTS RESERVED ii COMMITTEE MEMBERSHIP TITLE: Arroyo Toad (Anaxyrus californicus) Life History, Population Status, Population Threats, and Habitat Assessment of Conditions at Fort Hunter Liggett, Monterey County, California AUTHOR: Jacquelyn Petrasich Hancock DATE SUBMITTED: December 2009 COMMITTEE CHAIR: David Pilliod, PhD COMMITTEE MEMBER: Emily Taylor, PhD COMMITTEE MEMBER: Scott Steinmaus, PhD iii Abstract Arroyo Toad (Anaxyrus californicus) Life History, Population Status, Population Threats, and Habitat Assessment of Conditions at Fort Hunter Liggett, Monterey County, California Jacquelyn Petrasich Hancock The arroyo toad (Anaxyrus californicus) is a federally endangered species found on Fort Hunter Liggett, Monterey County, California. The species was discovered in 1996 and was determined to occupy 26.7 km of the San Antonio River from approximately 2.4 km northwest of the San Antonio Mission de Padua, to the river delta above the San Antonio Reservoir. The construction of the San Antonio Reservoir dam in 1963 isolated this northern population of arroyo toads. Through time, the Fort Hunter Liggett landscape has changed drastically. The land was heavily grazed by cattle until 1991, which considerably reduced vegetation in riparian areas. Military training following acquisition of the land in 1940 far exceeded current allowable training. Fire was used extensively to reduce unfavorable vegetation, and as a result, extreme tree loss occurred through the ranges. -
(Tantilla Oolitica) in Miami-Dade and Monroe Counties, Florida
Assessment of the Status and Distribution of the Endemic Rim Rock Crowned Snake (Tantilla oolitica) in Miami-Dade and Monroe Counties, Florida Final Report Grant Agreement #401817G006 Kirsten N. Hines and Keith A. Bradley July 10, 2009 Submitted by: The Institute for Regional Conservation 22601 S.W. 152 Avenue, Miami, FL 33170 George D. Gann, Executive Director Submitted to: Paula Halupa Fish and Wildlife Biologist U.S. Fish and Wildlife Service 1339 20th Street Vero Beach, FL 32960 1 Project Background: The rim rock crowned snake (Tantilla oolitica) is one of three species of small, burrowing snakes within the genus Tantilla found in Florida. Of the more than 40 species of this genus extending from the southeastern United States down to northern Argentina in South America, T. oolitica has the most limited distribution (Wilson 1982, Scott 2004). Confined to the Miami Rock Ridge in southeastern Miami-Dade County and parts of the Florida Keys in Monroe County, this species has been greatly affected by the rapid urbanization of this area. By 1975 it had already made the Florida State list of threatened species and it is currently considered a candidate for the Federal Endangered Species List. Traditionally, T. oolitica habitat included rockland hammocks and pine rocklands. Less than 2% of the pine rocklands on the Miami Rock Ridge currently remain (Snyder et. al 1990, USFWS 1999) and rockland hammocks both in Miami-Dade County and throughout the Florida Keys have been reduced to less than half their original extent and continue to face threat of development (Enge et. al 1997, USFWS 1999). -
02186714 Colombia Finalrepo
2 TABLE OF CONTENTS Project partners & Collaborators ...................................................................................................................................... 3 SECTION 1 ....................................................................................................................................................................... 4 Summary ............................................................................................................................................................................... 4 Introduction ......................................................................................................................................................................... 4 Project members ................................................................................................................................................................. 6 SECTION 2 .....................................................................................................................................................................10 Aim and objectives ......................................................................................................................................................10 Changes to original project plan ...............................................................................................................................10 Methodology ................................................................................................................................................................11 -
Trade in Live Reptiles, Its Impact on Wild Populations, and the Role of the European Market
BIOC-06813; No of Pages 17 Biological Conservation xxx (2016) xxx–xxx Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/bioc Review Trade in live reptiles, its impact on wild populations, and the role of the European market Mark Auliya a,⁎,SandraAltherrb, Daniel Ariano-Sanchez c, Ernst H. Baard d,CarlBrownd,RafeM.Browne, Juan-Carlos Cantu f,GabrieleGentileg, Paul Gildenhuys d, Evert Henningheim h, Jürgen Hintzmann i, Kahoru Kanari j, Milivoje Krvavac k, Marieke Lettink l, Jörg Lippert m, Luca Luiselli n,o, Göran Nilson p, Truong Quang Nguyen q, Vincent Nijman r, James F. Parham s, Stesha A. Pasachnik t,MiguelPedronou, Anna Rauhaus v,DannyRuedaCórdovaw, Maria-Elena Sanchez x,UlrichScheppy, Mona van Schingen z,v, Norbert Schneeweiss aa, Gabriel H. Segniagbeto ab, Ruchira Somaweera ac, Emerson Y. Sy ad,OguzTürkozanae, Sabine Vinke af, Thomas Vinke af,RajuVyasag, Stuart Williamson ah,1,ThomasZieglerai,aj a Department Conservation Biology, Helmholtz Centre for Environmental Conservation (UFZ), Permoserstrasse 15, 04318 Leipzig, Germany b Pro Wildlife, Kidlerstrasse 2, 81371 Munich, Germany c Departamento de Biología, Universidad del Valle de, Guatemala d Western Cape Nature Conservation Board, South Africa e Department of Ecology and Evolutionary Biology,University of Kansas Biodiversity Institute, 1345 Jayhawk Blvd, Lawrence, KS 66045, USA f Bosques de Cerezos 112, C.P. 11700 México D.F., Mexico g Dipartimento di Biologia, Universitá Tor Vergata, Roma, Italy h Amsterdam, The Netherlands