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Zootaxa, Molecular Phylogeny, Classification, and Biogeography Of
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. -
B.Sc. II YEAR CHORDATA
B.Sc. II YEAR CHORDATA CHORDATA 16SCCZO3 Dr. R. JENNI & Dr. R. DHANAPAL DEPARTMENT OF ZOOLOGY M. R. GOVT. ARTS COLLEGE MANNARGUDI CONTENTS CHORDATA COURSE CODE: 16SCCZO3 Block and Unit title Block I (Primitive chordates) 1 Origin of chordates: Introduction and charterers of chordates. Classification of chordates up to order level. 2 Hemichordates: General characters and classification up to order level. Study of Balanoglossus and its affinities. 3 Urochordata: General characters and classification up to order level. Study of Herdmania and its affinities. 4 Cephalochordates: General characters and classification up to order level. Study of Branchiostoma (Amphioxus) and its affinities. 5 Cyclostomata (Agnatha) General characters and classification up to order level. Study of Petromyzon and its affinities. Block II (Lower chordates) 6 Fishes: General characters and classification up to order level. Types of scales and fins of fishes, Scoliodon as type study, migration and parental care in fishes. 7 Amphibians: General characters and classification up to order level, Rana tigrina as type study, parental care, neoteny and paedogenesis. 8 Reptilia: General characters and classification up to order level, extinct reptiles. Uromastix as type study. Identification of poisonous and non-poisonous snakes and biting mechanism of snakes. 9 Aves: General characters and classification up to order level. Study of Columba (Pigeon) and Characters of Archaeopteryx. Flight adaptations & bird migration. 10 Mammalia: General characters and classification up -
Classification of a Clade of New World Doves (Columbidae: Zenaidini)
Zootaxa 3669 (2): 184–188 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Correspondence ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3669.2.11 http://zoobank.org/urn:lsid:zoobank.org:pub:183526F0-B925-49EA-B2C6-49520634452A Classification of a clade of New World doves (Columbidae: Zenaidini) RICHARD C. BANKS1, JASON D. WECKSTEIN2, J.V. REMSEN, JR3 & KEVIN P. JOHNSON4 13201 Circle Hill Rd., Alexandria, VA 22305, USA. E-mail: [email protected] 2Field Museum of Natural History, Chicago, IL 60605 USA. E-mail [email protected] 3Museum of Natural Science and Dept. Biological Sciences, Louisiana State University, Baton Rouge, LA 70776 USA. E-mail: [email protected] 4Illinois Natural History Survey, University of Illinois, Champaign, IL 61820 USA. E-mail: [email protected] To evaluate the role of the formation of the Central American land bridge in diversification of the American avifauna, Johnson and Weckstein (2011) reconstructed a phylogeny, using DNA sequence data from four gene regions, of 24 nominal species in three putative genera of New World doves. Although a systematic revision of these doves was not a primary purpose of their study, Johnson and Weckstein (2011) provided information that helps to re-evaluate the presumed relationships among the taxa included. Their analysis supported a hypothesis of monophyly for a group containing seven species currently (American Ornithologists’ Union [AOU] 1998, Gibbs et al. 2001, Dickinson 2003, Remsen et al. 2012) placed in the genus Zenaida Bonaparte, 1838, and for a group of 12 taxa in 6 species (of as many as 11 currently recognized species) in the genus Leptotila Swainson, 1837 (Gibbs et al. -
Assessing the Extinction Probability of the Purple-Winged Ground Dove, an Enigmatic Bamboo Specialist
fevo-09-624959 April 29, 2021 Time: 12:42 # 1 ORIGINAL RESEARCH published: 29 April 2021 doi: 10.3389/fevo.2021.624959 Assessing the Extinction Probability of the Purple-winged Ground Dove, an Enigmatic Bamboo Specialist Alexander C. Lees1,2*, Christian Devenish1, Juan Ignacio Areta3, Carlos Barros de Araújo4,5, Carlos Keller6, Ben Phalan7 and Luís Fábio Silveira8 1 Ecology and Environment Research Centre (EERC), Department of Natural Sciences, Manchester Metropolitan University, Manchester, United Kingdom, 2 Cornell Lab of Ornithology, Cornell University, Ithaca, NY, United States, 3 Laboratorio de Ecología, Comportamiento y Sonidos Naturales, Instituto de Bio y Geociencias del Noroeste Argentino (IBIGEO-CONICET), Salta, Argentina, 4 Programa de Pós-Graduação em Ecologia e Monitoramento Ambiental, Centro de Ciências Aplicadas e Educação, Universidade Federal da Paraíba, Rio Tinto, Brazil, 5 Programa de Pós-graduação em Ciências Biológicas, Universidade Estadual de Londrina, Londrina, Brazil, 6 Independent Researcher, Rio de Janeiro, Brazil, 7 Centre for Conservation of Atlantic Forest Birds, Parque das Aves, Foz do Iguaçu, Brazil, 8 Seção de Aves, Museu de Zoologia da Universidade de São Paulo, São Paulo, Brazil The continued loss, fragmentation, and degradation of forest habitats are driving an Edited by: extinction crisis for tropical and subtropical bird species. This loss is particularly acute in Bruktawit Abdu Mahamued, the Atlantic Forest of South America, where it is unclear whether several endemic bird Kotebe Metropolitan University (KMU), Ethiopia species are extinct or extant. We collate and model spatiotemporal distributional data Reviewed by: for one such “lost” species, the Purple-winged Ground Dove Paraclaravis geoffroyi, John Woinarski, a Critically Endangered endemic of the Atlantic Forest biome, which is nomadic Charles Darwin University, Australia Sam Turvey, and apparently dependent on masting bamboo stands. -
A Synopsis of the Pre-Human Avifauna of the Mascarene Islands
– 195 – Paleornithological Research 2013 Proceed. 8th Inter nat. Meeting Society of Avian Paleontology and Evolution Ursula B. Göhlich & Andreas Kroh (Eds) A synopsis of the pre-human avifauna of the Mascarene Islands JULIAN P. HUME Bird Group, Department of Life Sciences, The Natural History Museum, Tring, UK Abstract — The isolated Mascarene Islands of Mauritius, Réunion and Rodrigues are situated in the south- western Indian Ocean. All are volcanic in origin and have never been connected to each other or any other land mass. Despite their comparatively close proximity to each other, each island differs topographically and the islands have generally distinct avifaunas. The Mascarenes remained pristine until recently, resulting in some documentation of their ecology being made before they rapidly suffered severe degradation by humans. The first major fossil discoveries were made in 1865 on Mauritius and on Rodrigues and in the late 20th century on Réunion. However, for both Mauritius and Rodrigues, the documented fossil record initially was biased toward larger, non-passerine bird species, especially the dodo Raphus cucullatus and solitaire Pezophaps solitaria. This paper provides a synopsis of the fossil Mascarene avifauna, which demonstrates that it was more diverse than previously realised. Therefore, as the islands have suffered severe anthropogenic changes and the fossil record is far from complete, any conclusions based on present avian biogeography must be viewed with caution. Key words: Mauritius, Réunion, Rodrigues, ecological history, biogeography, extinction Introduction ily described or illustrated in ships’ logs and journals, which became the source material for The Mascarene Islands of Mauritius, Réunion popular articles and books and, along with col- and Rodrigues are situated in the south-western lected specimens, enabled monographs such as Indian Ocean (Fig. -
P0896-P0903.Pdf
The Condor 95:896-903 0 The Cooper Omlthological Society 1993 SPATIAL AND TEMPORAL ABUNDANCE PATTERNS OF RUDDY QUAIL-DOVES (GEOTRYGON MOKWVi4) NEAR MANAUS, BRAZIL’ PHILIP C. STOUFFER~ AND RICHARD 0. BIERREGAARD, JR. BiodiversityPrograms, NHB 180, SmithsonianInstitution, Washington,DC 20560 Abstract. We analyzed patterns of abundanceof Ruddy Quail-Doves (Geotrygonmon- tana) based on 12 years of mist-net data (457 captures)from terrajirme forest near Manaus in central Amazonian Brazil. Unlike most understory birds at the study site, G. montana varied greatly in abundance. Quail-doves disappeared for months and then reappeared, usually during the wet season.In some months they became one of the most frequently netted birds. Quail-doves avoided isolated forest fragments of one ha, although abundance did not differ among fragments of 10 ha, 100 ha, and continuous forest. Peak abundance varied among years, as did the timing of peak abundance.In general,the annual pattern of quail-dove abundance was correlated with the annual rainfall pattern. Considering all 12 years of data, however, quail-dove abundanceduring a given three-month period was not correlatedwith rainfall during that period, but with rainfall in the sameperiod in the previous year. No quail-doves were recaptured more than a few weeks apart; thus individual birds did not return to the same site from year to year. Since quail-doves feed mainly on fallen fruit, these resultssuggest that they may range over wide areasto exploit regional differences in fruit production. Key words: Amazonian Brazil; Geotrygonmontana; migration; rainfall; Ruddy Quail- Dove:seasonal movements. INTRODUCTION portunity for relatively short distance altitudinal The understoty bird community of terra firme migration suchas is common in Central America forest in central Amazonian Brazil is character- (Levey 1988a, Stiles 1988, Loiselle and Blake ized by permanently resident species that show 199 1) and southeasternBrazil (Sick 1983). -
Species Present in the Barachois
2017 Species Present in the Barachois Antoine Rivière Internship of “the Barachois Project” EPCO 7/25/2017 Table of Contents Chapter 1: Sedentary Birds............................................................................................................................ 3 Scientific Name: Zosterops mauritianus ....................................................................................................... 4 Scientific Name: Foudia rubra (rare in the barchois) .................................................................................... 5 Scientific Name: Butorides striatus ............................................................................................................... 6 Scientific Name: Foudia Madagascariensis................................................................................................... 7 Scientific Name: Nesoenas picturata ............................................................................................................ 8 Scientific Name: Acridotheres tristis ............................................................................................................. 9 Scientific Name: Pycnonotus jocosus .......................................................................................................... 10 Scientific Name: Estrilda astrild .................................................................................................................. 11 Scientific Name: Ploceus cucullatus ........................................................................................................... -
Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose -
Geotrygon Mystacea ) for St
J. Carib. Ornithol. 20:45-46, 2007 FIRST RECORD OF BRIDLED QUAIL-DOVE ( GEOTRYGON MYSTACEA ) FOR ST. MARTIN 1,2 1 ADAM B ROWN AND R ICK N EWMAN 1Environmental Protection in the Caribbean, 200 Dr. Martin Luther King Jr. Blvd., Riviera Beach, FL 33404, USA: 2email: [email protected] Abstract : We document the first record of Bridled Quail-Dove ( Geotrygon mystacea ) for St. Martin. An adult male was observed on the northwest slope of Pic Paradis on 22 January and subsequently captured and banded on 3 Febru- ary 2006. Key words: Bridled Quail-Dove, distributional record, Geotrygon mystacea , Lesser Antilles, St. Martin Resumen: PRIMER R EGISTRO DE LA P ERDIZ DE M ARTINICA ( GEOTRYGON MYSTACEA ) EN S T. M ARTIN . Se documenta el primer reGistro de la Perdiz de Martinica ( Geotrygon mystacea ) para St. Martin. La especie fue observada en las cuestas del noroeste de Pic Paradis el 22 de enero y después fue capturado y anillado el 3 de febrero de 2006. Palabras clave: Antillas Menores, distributional record, Geotrygon mystacea , St. Martin Résumé : PREMIÈRE OBSERVATION DE LA C OLOMBE À CROISSANTS ( GEOTRYGON MYSTACEA ) POUR S AINT -MARTIN . Nous fournissons des informations sur la première observation pour Saint-Martin de la Colombe à croissants (Geotrygon mystacea ). Un mâle adulte a été observé le 22 janvier 2006 sur les pentes nord du Pic Paradis puis a été capturé et baGué le 3 février. Mots-clés : Colombe à croissants, distribution, Geotrygon mystacea , Petites Antilles, Saint-Martin THE B RIDLED Q UAIL -DOVE ( Geotrygon mysta- characteristics. cea ) is considered a species of concern by BirdLife On 2 February 2006, Bertrand Jno Baptiste (BJB) International due to its restricted ranGe from eastern and Adam Brown (AB) observed a Bridled Quail- Puerto Rico south to St. -
0617 Hyspirhynchus H Ferox.Pdf (2.790Mb)
REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE Catalogue of American Amphibians and Reptiles. -wr -7 Sosa, R A., R.W.Henderson, and R Powell 1995. Hyspi- I rhynchus, H. ferox. r- J f r* * - *.I Hypsirhynchus Giinther -. Hypsrrhynchus Gunther, 1858:49. Type-spec~es,Hypsrrhynchus ferox Gunther, 1858, by monotypy. Content. A single specles, Hypsrrhynchus ferox, IS recog- nized Figure. An adult male Hvpsirhyrlchus ferox ferox (Bobby Witcher Memorial Collection, BWMC 06027) from 4.3 km NE Definition. Hypsirhynchus ferox is a moderately large (maxi- Oviedo, Provincia de Pedernales, Repliblica Dominicana. Note mum SVL of males to 727 mm, of females to 773 mm) the upturned snout. xenodontine with 19 (exceptionally 17 or 21) scale rows at midbody; 156-177 ventrals and 73-93 paired subcaudals in males, 162- 182 ventrals and 7 1-89 paired subcaudals in females; distal, and arranged in four longitudinal series, the lateral series smooth dorsal scales with a single, often very prominent apical delimiting the non-sulcate from the sulcate surface; The non- pit; divided anal (= cloacal); and a somewhat elongate head with sulcate surface is covered with many very small spines and normal unspecialized colubrid type head scalation: loreals 111 spinules which extend onto the sulcate surface to the sulci. The or 010 (occasionally 110) modally by population, 111 preoculars, sulcate surface (between sulci) is very weakly rugose. The sul- 22(rarely 111 or 112) postoculars, usually 1 + 2 temporals, usu- cus spermaticus is divided very near the base of the organ, the ally 818 supralabials, and usually 10110 infralabials. two grooves extending to just below the apices of the two distal The dorsal pattern is variable, ranging from uniformly pink- forks; apices are calyculate, the margins of the calyces studded ish buff to tan to heavily patterned with a median series of ar- with prominent papillae. -
Mourning Doves in Florida1 William M
WEC 226 Mourning Doves in Florida1 William M. Giuliano, James F. Selph, Kurt Hodges, and Nick Wiley2 While many species of dove live in Florida, the mourning include the diamond dove (Geopelia cuneate), ringed turtle dove (Zenaida macroura) is the only dove species native to dove (Streptopelia risoria), rock dove or common pigeon the state (Figure 1). (Columba livia), and Eurasian collared or ring-necked dove (Streptopelia decaocto). Being the most widely distributed and only native species of dove in Florida, mourning doves will be the focus of this report. Distribution and Status Mourning doves can be found throughout southern Canada, all of the U.S. and Central America, and most of the Caribbean Islands. Found throughout Florida, the greatest numbers of mourning doves appear to be in the central portion of the state. Florida populations increase during the winter months, when the resident population is supplemented by birds migrating in from the north. During the past 40 years, dove populations have remained relatively Figure 1. Mourning doves are the most widely distributed and only stable in the eastern U.S., with a 1% increase during the native species of dove in Florida. last 10 years. In Florida, dove populations increased by 2% Credits: J. C. Leupold, U.S. Fish and Wildlife Service during the past 40 years, but decreased slightly (2%) during Many dove species that reside in Florida, while not native, the last 10 years. Throughout the U.S., the number of dove are state and federally protected, including the common hunters and birds harvested annually has been declining. -
Remarks on the Taxonomy of Some American Doves
330 •.vo•F Auk• REMARKS ON THE TAXONOMY OF SOME AMERICAN DOVES BY DI•RI•K GOODWIN In the courseof current examinationand re-arrangementof the pigeons in the collection of the British Museum (Natural History) certain conclusionshave been reachedon the status of severalAmerican genera, which somewhat differ from current treatment. Zenaida, Zenaidura, Nesopelia, Melopelia In his catalogueof the pigeonsSalvadori (1893) listed the four genera Zenaida, Zenaidura, Nesopelia and Melopelia in his sub-family Zen- aidinae. He distinguished the first two as having "moderate and straight" bills and fourteen tail feathers, the tail of Zenaidura being "rather long, graduatedor cuneate"and that of Zenaida "moderateand rounded". Nesopelia(containing the GalapagosDove) he characterised as having twelve tail feathers, a "rather short and rounded" tail and the bill "rather long and much bent downwards",Melopelia (the White- winged Dove) on its lack of certain signal markings and possession of others, and also on slight differencesin the shapeof the inner webs of the first two primaries. Ridgway (1916) followedthis classification. Peters(1934) pointedout that only oneof the species,the SouthAmerican auriculata, placed in Zenaida by theseauthors had in fact fourteen tail feathers,the othershaving twelve. He accordinglyplaced auriculata in the genus Zenaidura. He made Melopelia congenericwith Zenaida, remarking that he had looked in vain for any characters "of generic value" to separate them. He maintained Nesopeliaby reason of its "short tail... and strongly decurved bill". Hellmayr and Conover (1942) followedPeters, placing the Mourning Dove Zenaidura macroura (Linnaeus) and the Eared Dove Z. auriculata (Des Murs) in Zenaidura; the Zenaida Dove Zenaida aurita (Temminck) and the White-winged Dove Z.