Status of West Indian Racers in the Lesser Antilles
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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 The addition of Anolis cristatellus to species lists of Dominica has made many guides and species lists outdated.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. -
Biological and Proteomic Analysis of Venom from the Puerto Rican Racer (Alsophis Portoricensis: Dipsadidae)
Toxicon 55 (2010) 558–569 Contents lists available at ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Biological and proteomic analysis of venom from the Puerto Rican Racer (Alsophis portoricensis: Dipsadidae) Caroline L. Weldon, Stephen P. Mackessy* School of Biological Sciences, University of Northern Colorado, 501 20th Street, CB 92, Greeley, CO 80639-0017, USA article info abstract Article history: The Puerto Rican Racer Alsophis portoricensis is known to use venom to subdue lizard prey, Received 12 August 2009 and extensive damage to specific lizard body tissues has been well documented. The Received in revised form toxicity and biochemistry of the venom, however, has not been explored extensively. We 27 September 2009 employed biological assays and proteomic techniques to characterize venom from Accepted 2 October 2009 A. portoricensis anegadae collected from Guana Island, British Virgin Islands. High metal- Available online 14 October 2009 loproteinase and gelatinase, as well as low acetylcholinesterase and phosphodiesterase activities were detected, and the venom hydrolyzed the a-subunit of human fibrinogen Keywords: Biological roles very rapidly. SDS-PAGE analysis of venoms revealed up to 22 protein bands, with masses of w Colubrid 5–160 kDa; very little variation among individual snakes or within one snake between CRISP venom extractions was observed. Most bands were approximately 25–62 kD, but MALDI- Enzymes TOF analysis of crude venom indicated considerable complexity in the 1.5–13 kD mass a-Fibrinogenase range, including low intensity peaks in the 6.2–8.8 kD mass range (potential three-finger Gland histology toxins). MALDI-TOF/TOF MS analysis of tryptic peptides confirmed that a 25 kDa band was Hemorrhage a venom cysteine-rich secretory protein (CRiSP) with sequence homology with tigrin, Mass spectrometry a CRiSP from the natricine colubrid Rhabdophis tigrinus. -
Alsophis Rijgersmaei Cope, 1869 (Squamata: Dipsadidae) Sur L'île De
Questel K. (2021). Alsophis rijgersmaei Cope, 1869 (Squamata: Dipsadidae) sur l’île de Saint-Barthélemy. Mise à jour : janvier 2021. Bulletin de l’ATE numéro 7. 8p. 1 Karl Questel Le Bulletin de l’ATE numéro 7 Mise à jour : Janvier 2021 Alsophis rijgersmaei Cope, 1869 (Squamata: Dipsadidae) sur l’île de Saint-Barthélemy Ceci est la version basse définition pour le web. Si vous souhaitez une version haute définition pour l'impression, veuillez demander à : [email protected] This is the low definition version for the web. If you want a high definition version for printing, please request to : [email protected] 2 Questel K. (2021). Alsophis rijgersmaei Cope, 1869 (Squamata: Dipsadidae) sur l’île de Saint-Barthélemy. Mise à jour : janvier 2021. Bulletin de l’ATE numéro 7. 8p. Alsophis rijgersmaei en bref / Alsophis rijgersmaei in short. La plus grande taille documentée. - 108 cm (du museau au cloaque (LV) - Snout to vent (SVL)) Largest documented size. - 138 cm (du museau au bout de la queue (LT) - Snout to the end of the tail (TL)). Une femelle. A female. Nombre d’écailles ventrales et ♀ -Ventrales, ventral : 197-206. sous-caudales par sexes identifiés (Min-Max). -Sous-caudales, sub-caudal : 93-102. Number of ventral and sub-caudal scales ♂ -Ventrales, ventral : 201-208. by identified sexes (Min-Max). -Sous-caudales, sub-caudal : 109-117. Moyennes générales de toutes les données ♀+♂+? -Ventrales, ventral : 197-208. disponibles: mâles, femelles et non sexés -Sous-caudales, sub-caudal : 93-122. (Min-Max). (Saint-Barthélemy, Saint-Martin, Anguilla) General averages of all available data: males, females and not sexed (Min-Max). -
The Antiguan Racer Alsophis Antiguae
Oryx Vol 35 No 2 April 2001 Five years of conserving the 'world's rarest snake', the Antiguan racer Alsophis antiguae Jenny C. Daltry, Quentin Bloxam, Gillian Cooper, Mark L. Day, John Hartley, McRonnie Henry, Kevel Lindsay and Brian E. Smith Abstract The Critically Endangered Antiguan racer evidently benefited from the project's rat eradication Alsophis antiguae is confined to Great Bird Island, a 9.9- programme. The snakes are still seriously threatened by ha (24.5-acre) islet off the north-east coast of Antigua in other intrinsic and extrinsic factors, however, including the Lesser Antilles. This island represents well under inbreeding depression, frequent hurricanes, invasive 0.1 per cent of the species's historical distribution range. predators and deliberate killing by tourists, as well as During the past 5 years, the total number of racers aged the problem that Great Bird Island is too small to 1 year or more has fluctuated between 51 and 114, and support more than about 100 individuals. This paper currently stands at approximately 80. Since 1995, the describes the activities and impact of this project to date, Antiguan Racer Conservation Project (ARCP) has en- and outlines a series of conservation activities to deavoured to save this harmless snake from extinction safeguard the long-term future of the species, which by using a combination of education, conservation include reintroduction of the Antiguan racer to restored breeding, habitat restoration, local capacity building islands within its former distribution range. and applied research. The Antiguan racer's ecology and population dynamics have become well understood Keywords Alsophis, Antigua, Antiguan racer, conser- after 5 years of intensive study, and the species has vation, invasive species, reintroduction. -
Fossil Dipsadid Snakes from the Guadeloupe Islands (French West-Indies) and Their Interactions with Past Human Populations
geodiversitas 2019 ● 41 ● 12 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 : Bruno David, Président du Muséum national d’Histoire naturelle RÉDACTEUR EN CHEF / EDITOR-IN-CHIEF : Didier Merle ASSISTANTS DE RÉDACTION / ASSISTANT EDITORS : Emmanuel Côtez ([email protected]) ; Anne Mabille MISE EN PAGE / PAGE LAYOUT : Emmanuel Côtez COMITÉ SCIENTIFIQUE / SCIENTIFIC BOARD : Christine Argot (MNHN, 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 (UPMC, Paris) Gaël Clément (MNHN, Paris) Ted Daeschler (Academy of Natural Sciences, Philadelphie) Bruno David (MNHN, 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 (UPMC, Paris) Sevket Sen (MNHN, Paris) Stanislav Štamberg (Museum of Eastern Bohemia, Hradec Králové) Paul Taylor (The Natural History Museum, Londres) COUVERTURE / COVER : Background: made from the Figures of the article; medallion: Jean-Claude Rage, to whom this issue is dedicated. Geodiversitas est indexé dans / Geodiversitas is indexed in: – Science Citation Index Expanded (SciSearch®) – ISI Alerting Services® – Current Contents® / Physical, Chemical, and Earth Sciences® -
Geographic Variation in the Bahamian Brown Racer, Alsophis Vudii A
Geographic Variation in the Bahamian Brown Racer, Alsophis Vudii A thesis presented to the faculty of the College of Arts and Sciences of Ohio University In partial fulfillment of the requirements for the degree Master of Science Christina Wieg June 2009 © June 2009 Christina Wieg. All Rights Reserved. This thesis entitled Geographic Variation in the Bahamian Brown Racer, Alsophis Vudii by CHRISTINA WIEG has been approved for the Program of Environmental Studies and the College of Arts and Sciences by Matthew W. White Associate Professor of Biological Science Benjamin M. Ogles Dean, College of Arts and Sciences Abstract WIEG, CHRISTINA, M.S., June 2009, Environmental Studies GEOGRAPHIC VARIATION IN THE BAHAMIAN BROWN RACER, ALSOPHIS VUDII (48 pp.) Director of Thesis: Matthew M. White Nine meristic and fourteen morphometric characters were examined to determine geographic variation in the five subspecies of the insular snake species, Alsophis vudii. In addition, museum specimens from the closely derived species Alsophis cantherigerus were examined. Canonical discriminate analysis determined that, based on the morphological data, significant differences were observed among subspecies. However, significant differences were also observed between island populations. My results suggest that the current subspecies designations oversimplify the variation within the species and are not an adequate reflection of variation present among the island populations. Additional research is required in order to determine the causes of the observed variation within the species. Possible explanations for observed variation may include multiple colonization events or environmental variation among islands. Approved: Matthew M. White Associate Professor of Biological Sciences Dedication I dedicate this work to my husband, Rick Perkins. -
Colubrid Venom Composition: an -Omics Perspective
toxins Review Colubrid Venom Composition: An -Omics Perspective Inácio L. M. Junqueira-de-Azevedo 1,*, Pollyanna F. Campos 1, Ana T. C. Ching 2 and Stephen P. Mackessy 3 1 Laboratório Especial de Toxinologia Aplicada, Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Instituto Butantan, São Paulo 05503-900, Brazil; [email protected] 2 Laboratório de Imunoquímica, Instituto Butantan, São Paulo 05503-900, Brazil; [email protected] 3 School of Biological Sciences, University of Northern Colorado, Greeley, CO 80639-0017, USA; [email protected] * Correspondence: [email protected]; Tel.: +55-11-2627-9731 Academic Editor: Bryan Fry Received: 7 June 2016; Accepted: 8 July 2016; Published: 23 July 2016 Abstract: Snake venoms have been subjected to increasingly sensitive analyses for well over 100 years, but most research has been restricted to front-fanged snakes, which actually represent a relatively small proportion of extant species of advanced snakes. Because rear-fanged snakes are a diverse and distinct radiation of the advanced snakes, understanding venom composition among “colubrids” is critical to understanding the evolution of venom among snakes. Here we review the state of knowledge concerning rear-fanged snake venom composition, emphasizing those toxins for which protein or transcript sequences are available. We have also added new transcriptome-based data on venoms of three species of rear-fanged snakes. Based on this compilation, it is apparent that several components, including cysteine-rich secretory proteins (CRiSPs), C-type lectins (CTLs), CTLs-like proteins and snake venom metalloproteinases (SVMPs), are broadly distributed among “colubrid” venoms, while others, notably three-finger toxins (3FTxs), appear nearly restricted to the Colubridae (sensu stricto). -
Diet of Six Species of Galapagos Terrestrial Snakes (Pseudalsophis Spp.) Inferred from Faecal Samples
Herpetology Notes, volume 12: 701-704 (2019) (published online on 02 July 2019) Diet of six species of Galapagos terrestrial snakes (Pseudalsophis spp.) inferred from faecal samples Luis Ortiz-Catedral1,*, Eli Christian1, Michael John Adam Skirrow1, Danny Rueda2, Christian Sevilla2, Kirtana Kumar1, Enzo M. R. Reyes1, and Jennifer C. Daltry3 The Galapagos terrestrial snakes, or ‘Galapagos Dialommus fuscus and Labrisomus denditricus) (Merlen racers’ (Pseudalsophis spp.) are a monophyletic group and Thomas, 2013). There are also unpublished reports of nine species within Dipsadidae, exclusively found of Galapagos racers ingesting large painted locusts in the Galapagos Islands (Zaher et al., 2018). A single (Schistocerca melanocera) (Jackson, 1993), and three continental species, P. elegans, is the closest relative of observers (park rangers from the Galapagos National these island species (Zaher et al., 2018), and is found Park) have witnessed P. dorsalis ingesting eggs of from Ecuador to Chile (Armendáriz, 1991; Carrillo de Galapagos doves (Zenaida galapagoensis) on Santa Espinoza and Icochea, 1995; Thomas, 1977). The group Fe Island (G. Quezada, M. Gavilanes and C. Gaona has been the subject of various taxonomic reviews pers. comm.). There is even an unconfirmed report of a since the early 1900s (Thomas, 1997). Although there terrestrial snake ingesting the fruit pulp of bitter melon have been significant advances in understanding the (Mormodica charantia) on Santa Cruz Island (Olesen evolutionary history of the group and their phylogenetic et al., 2018), but it is unknown whether the snake ate affinities (Grazziotin et al., 2012; Zaher et al., 2018), the bitter melon deliberately or by accident (e.g. while basic aspects of their biology have remained largely preying on a small vertebrate associated with the fruit). -
Zootaxa, Molecular Phylogeny, Classification, and Biogeography of West Indian Racer
Zootaxa 2067: 1–28 (2009) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2009 · Magnolia Press ISSN 1175-5334 (online edition) Molecular phylogeny, classification, and biogeography of West Indian racer snakes of the Tribe Alsophiini (Squamata, Dipsadidae, Xenodontinae) S. BLAIR HEDGES1, ARNAUD COULOUX2, & NICOLAS VIDAL3,4 1Department of Biology, 208 Mueller Lab, Pennsylvania State University, University Park, PA 16802-5301 USA. E-mail: [email protected] 2Genoscope. Centre National de Séquençage, 2 rue Gaston Crémieux, CP5706, 91057 Evry Cedex, France www.genoscope.fr 3UMR 7138, Département Systématique et Evolution, Muséum National d’Histoire Naturelle, CP 26, 57 rue Cuvier, 75005 Paris, France 4Corresponding author. E-mail : [email protected] Abstract Most West Indian snakes of the family Dipsadidae belong to the Subfamily Xenodontinae and Tribe Alsophiini. As recognized here, alsophiine snakes are exclusively West Indian and comprise 43 species distributed throughout the region. These snakes are slender and typically fast-moving (active foraging), diurnal species often called racers. For the last four decades, their classification into six genera was based on a study utilizing hemipenial and external morphology and which concluded that their biogeographic history involved multiple colonizations from the mainland. Although subsequent studies have mostly disagreed with that phylogeny and taxonomy, no major changes in the classification have been proposed until now. Here we present a DNA sequence analysis of five mitochondrial genes and one nuclear gene in 35 species and subspecies of alsophiines. Our results are more consistent with geography than previous classifications based on morphology, and support a reclassification of the species of alsophiines into seven named and three new genera: Alsophis Fitzinger (Lesser Antilles), Arrhyton Günther (Cuba), Borikenophis Hedges & Vidal gen. -
Cfreptiles & Amphibians
WWW.IRCF.ORG/REPTILESANDAMPHIBIANSJOURNALTABLE OF CONTENTS IRCF REPTILES & IRCFAMPHIBIANS REPTILES • VOL 15,& NAMPHIBIANSO 4 • DEC 2008 •189 27(1):105–106 • APR 2020 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS FEATURE ARTICLES Envenomation. Chasing Bullsnakes (Pituophis catenifer sayi ) ofin Wisconsin: a Puerto Rican Whiptail On the Road to Understanding the Ecology and Conservation of the Midwest’s Giant Serpent ...................... Joshua M. Kapfer 190 (Pholidoscelis. The Shared History of Treeboas exsul (Corallus grenadensis: )Teiidae) and Humans on Grenada: by a Puerto Rican A Hypothetical Excursion ............................................................................................................................Robert W. Henderson 198 RacerRESEARCH (Borikenophis ARTICLES portoricensis: Dipsadidae) . The Texas Horned Lizard in Central and Western Texas ....................... Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................in SouthernBrian J. Camposano, Kenneth L. Krysko, Puerto Kevin M. Enge, Ellen M. Donlan,Rico and Michael Granatosky 212 CONSERVATION ALERT Alejandro J. Sánchez Muñoz . World’s Mammals in Crisis ............................................................................................................................................................. 220 . More Than Mammals36 ...............................................................................................................................Calle -
REPTILIA: SQUAMATA: DACTYLOIDAE Anolis Gingivinus
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by UT Digital Repository 893.1 REPTILIA: SQUAMATA: DACTYLOIDAE Anolis gingivinus Catalogue of American Amphibians and Reptiles. Powell, R. and A.M. Bauer. 2012. Anolis gingivinus . Anolis gingivinus Cope Anguilla Bank Tree Anole Anolis gingivinus Cope 1864:170. Type-locality, “Anguilla Rock near Trinidad” (see Cope 1871), restricted by Lazell (1972) to Sandy Ground, Anguilla. Syntypes, British Museum of Natural History [now The Natural History Museum, London] (BMNH) 1946.8.29.15–20, BMNH 1946.8.29.15, an adult male, was designated the lectotype by Lazell (1980), the series was “pre - sented by W.J. Cooper to the British Museum” (not examined by authors). See Remarks . Anolis virgatus Garman 1887:41. Type-locality, “St.- Barthélémy.” Syntypes, Academy of Natural Sciences of Philadelphia (ANSP) 23007 (adult female), National Museum of Natural History (USNM) 39300 (an adult male), University of FIGURE 1. Adult male (top) and female Anolis gingivinus Michigan Museum of Zoology (UMMZ) 60243 from St. Martin (photographs by John S. Parmerlee, Jr.). (an adult male and a subadult), Museum of Comparative Zoology (MCZ) 6165 (MCZ-R- 171265–72, including at least one adult male), Barthélémy (Schwartz and Henderson 1991). An collected in 1884 by F. Lagois (not examined by introduced population of A. bimaculatus was reported authors). from St. Maarten by Powell et al. (1992), but that pop - Anolis krugi gingivinus : Barbour 1937:121. ulation is no longer extant (Powell et al. 2011). Anolis Anolis bimaculatus gingivinus : Underwood 1959:196. carolinensis was recently introduced to Anguilla Ctenonotus gingivinus : Schwartz and Henderson (Eaton et al. -
Fossil Vertebrates from Antigua, Lesser Antilles
Proc. Nati. Acad. Sci. USA Vol. 81, pp. 4448-4451, July 1984 Evolution Fossil vertebrates from Antigua, Lesser Antilles: Evidence for late Holocene human-caused extinctions in the West Indies (anthropology/island biogeography/vertebrate paleontology) DAVID W. STEADMAN*, GREGORY K. PREGILLt, AND STORRS L. OLSON* *National Museum of Natural History, Smithsonian Institution, Washington, DC 20560; and tNatural History Museum, P.O. Box 1390, San Diego, CA 92112 Communicated by Jared M. Diamond, March 30, 1984 ABSTRACT Vertebrate remains recovered from a lime- fissure was in an active working face of the quarry and was stone fissure filling on Antigua, Lesser Antilles, are associated presumably but a remnant of a larger cave or crevice that with radiocarbon dates ranging from 4300 to 2500 yr B.P., had been quarried away. Five stratigraphically concordant contemporaneous with the earliest aboriginal human occupa- radiocarbon ages range from 2560 ± 70 yr B.P. in the upper tion of the island. Nine taxa of lizards, snakes, birds, bats, and vertical unit to 4300 ± 150 yr B.P. in the lower vertical unit rodents (one-third of the total number of species represented (Table 1). Contemporaneity of man with the extinct fauna is as fossils) are either completely extinct or have never been re- demonstrated by the presence of shell remains of molluscan corded historically from Antigua. These extinctions came long food items and several lithic artifacts, including a blade from after any major climatic changes of the Pleistocene and are the horizontal portion of the fissure associated with a radio- best attributed to human-caused environmental degradation in carbon age of 3695 ± 100 yr B.P.