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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 The addition of Anolis cristatellus to species lists of Dominica has made many guides and species lists outdated.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. -
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). -
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® -
Status of West Indian Racers in the Lesser Antilles
ORYX VOL Status of West Indian racers in the Lesser Antilles Richard A. Sajdak and Robert W. Henderson The Lesser Antilles are home to four species of snakes of the genus Alsophis, otherwise known as racers. All four have undergone severe range reductions; at least two subspecies are extinct and another, A. antiguae, now occupies only 0.1 per cent of its historical range. The authors investigated the current distribution of the snakes by field surveys and interviews with the people of the islands. Insular snake species, from the Round Island most species-rich snake genus in the West boa to the Aruba Island rattlesnake, are promi- Indies (behind Typhlops and Tropidophis), and nent on lists of rare, threatened or extinct the second most wide ranging (after Typhlops). snakes. 'The risk of extinction decreases with It is the most species-rich and wide ranging increasing habitat size and population density. colubrid genus in the West Indies. Racers are a Therefore, island species with a spatially limit- conspicuous and important part of the ed habitat should be more vulnerable than Antillean herpetofauna. mainland species to extinction' (Dodd, 1987). During 1987, we made two trips of 30 days The Lesser Antilles (Figure 1) comprise a each to investigate the status of racers in the chain of 19 major islands and many satellite Lesser Antilles. The first, in January and islands in the Caribbean Sea between (but not February, was to St Martin (St Maartin), St including) the Virgin Islands in the north and Barts (St Barthelemy), St Kitts (St Christopher), Trinidad in the south. -
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. -
REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE ALSOPHISANTIGVAE N Catalogue of American Amphibians and Reptiles
632.1 REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE ALSOPHISANTIGVAE n Catalogue of American Amphibians and Reptiles. Henderson, R.W., R. Powell, J.C. Daltry, and M.L. Day. 1996. Alsophis antiguae. Abophis antiguae Parker Antiguan Racer Alsophis leucomelas antiguae Parker, 1933: 158. Spe-locality. "Antigua." Syntypes, British Museum of Natural History (BMNH) 1946.1.4.46, 1946.1.4.47 (re-registered numbers assigned after World War 11). juveniles, both females, col- lected by Mr. Gardiner, date of collection unknown (not examined by authors). Alsophis antiguae: Parker, 1936:228. Alsophis antillemis antiguae: Schwartz, 1966:216. Content. Two subspecies are recognized: A. a. antiguae and A. a. sajdaki. Definition. This moderately sized (maximum known SVL 71 1 mm) colubrid has 184-201 (males) or 185-201 (females) ventrals, 1 16- 126 (males) or 95- 105 (females) subcaudals, 19 (occasionally 21) dorsal scale rows at midbody, 818 supralabials, usually 10110 infralabials, 111 or 2J2 preoculars, 2J2 postoculars, 1+2J1+2 temporals, and 111 loreals. The frontal scute is long l and narrow. The cloacal scute (= anal plate) is divided. See I subspecific diagnoses for descriptions of dorsal and ventral color I and patterns. I Descriptions. In addition to those of Parker (1933, 1936), - descriptions are in Henderson (1989 [1990]) and Schwartz and Henderson (1 99 1). Illustrations. Lazell(1967) included a black-and-white ~ho- Map. Range of Alsophis antiguae (modified from ~chwartz tograph of an individual from Great Bird Island. Henderson and Henderson, 1991). ripe-localities are too imprecise to lot. (1989 [1990]) provided a black-and-white photograph of A. a. The nominate subspecies probably has been extirpated (see text), sa,daki and drawings illustrating the dorsal of A. -
Smithsonian Herpetological Information Servi Ce No
« .^•* ISUiWD/LISTS CZ? OF WEST INDIAN AKiPHIBIANS AND REPTILES D WILLIAM ?. MACLEAN, RICHARD KELLNER S HOWARD DENNIS COLLEGE OF THE VIRGIN ISLANDS ST. THOMAS, U.S. VIRGIN ISLANDS 00801 i SMITHSONIAN HERPETOLOGICAL INFORMATION SERVI CE NO. 40 1977 Division of Reptiles i Amphibians National Museum of Natural History Washington, DC 2056O INTRODUCTION The West Indian reptiles and amphibians are popular subjects of various kinds of biological research. These investigations will benefit greatly from Schwartz and Thomas' (1975) recent checklist, the first taxonomic summary in several decades. The present lists, which started as an ecology class project at the College of the Virgin Islands, are largely a compilation of Schwartz and Thomas' locality records. Our lists are useful in themselves, serve as a geographical index to Schwartz and Thomas, and should encourage more complete documentation of distributions. 627 islands are listed, some without records of reptiles or amphibians. Areas and maximum elevations are given vrtierever available. We have included everything that has a name, could support terrestrial vertebrates, and was not obviously a rock periodically awash. Even so, the list is far from complete. We have included the islands off the South and Central American coasts, many of which have more or less West Indian faunae and which are frequented by students of Antillean biota. Records from these islands are mostly from sources other than Schwartz and Thomas, as are a few in the Antilles proper. All such records are footnoted. We have not identified introduced species. Any student of these animals will immediately recognize the obvious introductions and will have personal opinions concerning the many nebulous cases. -
Iguana 12.2 B&W Text
VOLUME 12, NUMBER 2 JUNE 2005 ONSERVATION AUANATURAL ISTORY AND USBANDRY OF EPTILES IC G, N H , H R International Reptile Conservation Foundation www.IRCF.org GLENN MITCHELL Anegada or Stout Iguana (Cyclura pinguis) (see article on p. 78). JOHN BINNS RICHARD SAJDAK A subadult Stout Iguana (Cyclura pinguis) awaiting release at the head- Timber Rattlesnakes (Crotalus horridus) reach the northernmost extent starting facility on Anegada (see article on p. 78). of their range on the bluff prairies in Wisconsin (see article on p. 90). This cross-stitch was created by Anne Fraser of Calgary, Alberta from a photograph of Carley, a Blue Iguana (Cyclura lewisi) at the Captive Breeding Facility on Grand Cayman. The piece, which measures 6.8 x 4.2 inches, uses 6,100 stitches in 52 colors and took 180 hours to complete. It will be auctioned by the IRCF at the Daytona International Reptile Breeder’s Expo on 20 August 2005. Profits from the auction will benefit conser- vation projects for West Indian Rock Iguanas in the genus Cyclura. ROBERT POWELL ROBERT POWELL Red-bellied or Black Racers (Alsophis rufiventris) remain abundant on Spiny-tailed Iguanas (Ctenosaura similis) are abundant in archaeologi- mongoose-free Saba and St. Eustatius, but have been extirpated on St. cal zones on the Yucatán Peninsula. This individual is on the wall Christopher and Nevis (see article on p. 62). around the Mayan city of Tulúm (see article on p. 112). TABLE OF CONTENTS IGUANA • VOLUME 12, NUMBER 2 • JUNE 2005 61 IRCFInternational Reptile Conservation Foundation TABLE OF CONTENTS RESEARCH ARTICLES Conservation Status of Lesser Antillean Reptiles . -
Gastrointestinal Helminths of the Anole Anolis Oculatus(Polychridae)
J. Helminthol. Soc. Wash. 63(1), 1996, pp. 125-128 Research Note Gastrointestinal Helminths of the Anole Anolis oculatus (Polychridae) from Dominica, Lesser Antilles STEPHEN R. GOLDBERG! AND CHARLES R. BuRSEY2 1 Department of Biology, Whittier College, Whittier, California 90608, e-mail: [email protected], and 2 Department of Biology, Pennsylvania State University, Shenango Valley Campus, 147 Shenango Avenue, Sharon, Pennsylvania 16146, e-mail: [email protected] ABSTRACT: The gastrointestinal tracts of 20 Anolis 65.8 mm ± 11.5 (SD) (range 47-84 mm) and oculatus from Dominica, West Indies were examined consisted of 12 males (mean SVL = 73.4 mm ± for helminths. Eight helminth species were present: 7.7 [SD] and 8 females (mean SVL = 54.4 mm Ascarops sp., Oswaldocruzia lenteixelrai, Parapha- ryngodon cubensis, Physaloptera sp., Spauligodon cub- ± 3.9 [SD]). The mean SVLs of males and fe- ensis, Spinicauda spinicauda, Mesocoelium monas, and males are significantly different (Kruskal-Wallis Centrorhynchus sp. Juvenile acanthocephalans (Cen- statistic = 11.78, 1 df, P < 0.001). trorhynchus sp.) had the greatest prevalence (50%). The body cavity was opened by a longitudinal Spinicauda spinicauda had the highest mean intensity (33.5). All are new host records for A. oculatus. incision from throat to vent and the gastrointes- KEY WORDS: Polychridae, Anolis oculatus, Mesocoe- tinal tract was removed by cutting across the lium monas, Ascarops sp., Oswaldocruzia lenteixeirai, anterior esophagus and rectum. The esophagus, Parapharyngodon cubensis, Physaloptera sp., Spauli- stomach, small intestine, and large intestine were godon caymanensis, Spinicauda spinicauda, Centro- examined separately under a dissecting micro- rhynchus sp., prevalence, intensity. scope. -
Iguana B&W Text
Iguana 15.3 b&w text 9/10/08 5:43 AM Page 130 130 IGUANA • VOLUME 15, NUMBER 3 • SEPTEMBER 2008 DANIELLS ET AL. NATALIE N. WYSZYNSKI N. NATALIE Populations of Lesser Antillean Iguanas (Iguana delicatissima) have declined or disappeared on many islands. Those on Dominica are doing well and may serve as a model for developing management strategies for other islands (see IGUANA 14(4), p. 222). Iguana 15.3 b&w text 9/10/08 5:43 AM Page 131 AMPHIBIANS AND REPTILES OF DOMINICA IGUANA • VOLUME 15, NUMBER 3 • SEPTEMBER 2008 131 An Annotated Checklist of the Amphibians and Reptiles of Dominica, West Indies Esther A. Daniells1, Jeffrey W. Ackley2, Ruth E. Carter3, Peter J. Muelleman4, Seth M. Rudman5, Patrick A. Turk6, Nelson J. Vélez Espinet7, Lauren A. White8, and Natalie N. Wyszynski9 1Department of Biology, Colorado State University, Fort Collins, CO 80523 ([email protected]) 2Department of Biology, Eckerd College, St. Petersburg, FL 33711 ([email protected]) 3Department of Biology, Earlham College, Richmond, IN 47374 ([email protected]) 4Department of Biology, Truman State University, Kirksville, MO 63501 ([email protected]) 5Department of Biology, University of Rochester, Rochester, NY 14627 ([email protected]) 6Department of Biology, Avila University, Kansas City, MO 64145 ([email protected]) 7Department of Biology, University of Puerto Rico, Río Piedras, PR 00931 ([email protected]) 8Environmental Science Program, Oklahoma State University, Stillwater, OK 74078 [email protected]) 9Department of Psychology, University of Tennessee, Knoxville, TN 37996 ([email protected]) ! ravel writers have suggested that if Christopher Columbus Twere to take a Caribbean cruise today, Dominica might be the only West Indian island he would recognize. -
Herpetological Notes Xiv-Xvi
HERPETOLOGICAL NOTES XIV-XVI by Dr L. D. BRONGERSMA Rijksmuseum van Natuurlijke Historie, Leiden With i plate and i textfigure1) XIV. THE TYPES OF PSAMMOPHIS ANTILLENSIS SCHLEGEL, 1837 At the request of Dr K. P. Schmidt, Chicago, I recently examined the types of Psammophis antillensis Schl. This species as originally described was a composite, and it is, therefore, necessary to select a lectotype to restrict the name antillensis to one of the species involved. The difficulty is that Schlegel did not label his types as such, and that in most cases he did not mention how many specimens he actually examined. From the intro• duction to his Essai we know that Schlegel visited Paris, that the collections of the Museum National d'Histoire Naturelle were placed at his disposal, and that he was allowed to take the undescribed species with him to Leiden for further studies (Schlegel, 1837, I, p. XXIV). What happened in the case of Psammophis antillensis is probably this: in Paris Schlegel examined a series of snakes, which he believed to belong to an undescribed species; from this series he selected a few specimens which were taken to Leiden, and on these latter the description was based. The first point which must be settled is what specimens we are to consider as cotypes. In the present case there are two possibilities: 1. only those specimens upon which the description was actually based are cotypes; 2. all the specimens which were examined by Schlegel at Paris, as well as those at Leiden are cotypes 2). There is something to be said in favour of both points of view, but I believe 1) For the illustrations I am greatly indebted to Mr. -
CBD Fourth National Report
Fourth National Report to the Convention on Biological Diversity: ANTIGUA AND BARBUDA March 2010 Prepared by: Dr. Janil Gore Francis ANTIGUA AND BARBUDA – FOURTH NATIONAL REPORT TO THE CBD, 2009 ___________________________________________________________________________________________________________ 2 Table of Contents INTRODUCTION ..................................................................................................................................................................................................................................................12 BACKGROUND - FAUNA AND FLORA ...........................................................................................................................................................................................................13 AGRICULTURAL BIODIVERSITY ....................................................................................................................................................................................................................14 ECOSYSTEMS ........................................................................................................................................................................................................................................................17 COASTAL AND MARINE BIODIVERSITY - CRITICAL HABITATS ........................................................................................................................................................17 Coral Reefs ..................................................................................................................................................................................................................................................................19