Mapping Biodiversity in Cuba
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American Kestrel, Falco Sparverius
American Kestrel, Falco sparverius Status: State: Threatened Federal: Not listed Identification The American kestrel is the smallest and most widely distributed falcon in North America (Smallwood & Bird 2002, Hawk Mountain n.d.). At first glance, kestrels are often confused with other small birds such as mourning doves because of their propensity to perch on utility lines (Hawk Mountain n.d.). Kestrels however, have larger more roundish heads and often tip or “bob” their tails while perched. In flight, kestrels have a diagnostic flight pattern of quickly alternating between rapid wing beating and gliding. With proper lighting, their colorful plumage can further aid in positive identification. Kestrels are both sexually dimorphic and dichromatic; therefore sexing can be done at a distance and in chicks as young as three weeks (Hawk Mountain n.d.). Males are on average 10% smaller than females though this may be hard to ascertain in the field (Hawk Mountain 1997, Smallwood & Bird 2002). Males are more colorful, with bluish- gray wings (with or without black barring) and rufous (reddish-brown) tails. A single black bar tipped in white extends across the terminal end of the largely unmarked tail. Females are rufous on their wings and tails, often with multiple black bars extending horizontally along the length (Hawk Male American Kestrel Mountain n.d.). Plumage is highly variable © Jim Gilbert among individuals (Smallwood & Bird 2002). Both sexes exhibit grayish crowns and rufous crown patches with two vertical black stripes down their white cheeks. Black “eyespots on the back of their heads are thought to aid in reducing predation on kestrels by larger birds of prey- giving the illusion of predator awareness. -
Cuba Birding Tour – March 2017
CUBA BIRDING TOUR – MARCH 2017 By Chris Lotz Cuban Tody, photographed on this tour by Jean Kirkwood www.birdingecotours.com [email protected] 2 | T R I P R E P O R T Cuba Birding Tour: March 2017 This was another fantastic Cuban birding tour with a wonderful group of participants. We found all the Cuban and regional endemics we were targeting, except for Gundlach’s Hawk, and we also saw a truly excellent number of North American migrants, such as a plethora of colorful wood warblers. The smallest bird in the world, Bee Hummingbird, numerous Cuban Trogon and Cuban Tody sightings, and brilliant views of Blue-headed Quail-Dove, Grey-fronted Quail-Dove and Key West Quail-Dove were some of the many avian highlights. A map showing the route we take on our annual set departure Cuba trip – we do Jamaica as an extension and in future years we’ll be adding other Caribbean destinations such as the Dominican Republic Day 1, 1 March 2017. Arrival in Havana All nine of us arrived early before the tour was to officially begin tomorrow. From our comfortable base near Havana airport we already started getting nicely acquainted with some of the single-island and regional endemics. There was a Cuban Emerald nest right outside the back door of the place we stayed (http://www.donaamaliacuba.com/en/place) and Red- legged Thrush was very much in evidence (as it always is throughout Cuba, even in the middle of cities). Antillean Palm Swift winged its way overhead, and Cuban Pewee showed very well and gave its characteristic call. -
TAG Operational Structure
PARROT TAXON ADVISORY GROUP (TAG) Regional Collection Plan 5th Edition 2020-2025 Sustainability of Parrot Populations in AZA Facilities ...................................................................... 1 Mission/Objectives/Strategies......................................................................................................... 2 TAG Operational Structure .............................................................................................................. 3 Steering Committee .................................................................................................................... 3 TAG Advisors ............................................................................................................................... 4 SSP Coordinators ......................................................................................................................... 5 Hot Topics: TAG Recommendations ................................................................................................ 8 Parrots as Ambassador Animals .................................................................................................. 9 Interactive Aviaries Housing Psittaciformes .............................................................................. 10 Private Aviculture ...................................................................................................................... 13 Communication ........................................................................................................................ -
Wildlife of the North Hills: Birds, Animals, Butterflies
Wildlife of the North Hills: Birds, Animals, Butterflies Oakland, California 2005 About this Booklet The idea for this booklet grew out of a suggestion from Anne Seasons, President of the North Hills Phoenix Association, that I compile pictures of local birds in a form that could be made available to residents of the north hills. I expanded on that idea to include other local wildlife. For purposes of this booklet, the “North Hills” is defined as that area on the Berkeley/Oakland border bounded by Claremont Avenue on the north, Tunnel Road on the south, Grizzly Peak Blvd. on the east, and Domingo Avenue on the west. The species shown here are observed, heard or tracked with some regularity in this area. The lists are not a complete record of species found: more than 50 additional bird species have been observed here, smaller rodents were included without visual verification, and the compiler lacks the training to identify reptiles, bats or additional butterflies. We would like to include additional species: advice from local experts is welcome and will speed the process. A few of the species listed fall into the category of pests; but most - whether resident or visitor - are desirable additions to the neighborhood. We hope you will enjoy using this booklet to identify the wildlife you see around you. Kay Loughman November 2005 2 Contents Birds Turkey Vulture Bewick’s Wren Red-tailed Hawk Wrentit American Kestrel Ruby-crowned Kinglet California Quail American Robin Mourning Dove Hermit thrush Rock Pigeon Northern Mockingbird Band-tailed -
Dominican Republic Endemics of Hispaniola II 1St February to 9Th February 2021 (9 Days)
Dominican Republic Endemics of Hispaniola II 1st February to 9th February 2021 (9 days) Palmchat by Adam Riley Although the Dominican Republic is perhaps best known for its luxurious beaches, outstanding food and vibrant culture, this island has much to offer both the avid birder and general naturalist alike. Because of the amazing biodiversity sustained on the island, Hispaniola ranks highest in the world as a priority for bird protection! This 8-day birding tour provides the perfect opportunity to encounter nearly all of the island’s 32 endemic bird species, plus other Greater Antillean specialities. We accomplish this by thoroughly exploring the island’s variety of habitats, from the evergreen and Pine forests of the Sierra de Bahoruco to the dry forests of the coast. Furthermore, our accommodation ranges from remote cabins deep in the forest to well-appointed hotels on the beach, each with its own unique local flair. Join us for this delightful tour to the most diverse island in the Caribbean! RBL Dominican Republic Itinerary 2 THE TOUR AT A GLANCE… THE ITINERARY Day 1 Arrival in Santo Domingo Day 2 Santo Domingo Botanical Gardens to Sabana del Mar (Paraiso Caño Hondo) Day 3 Paraiso Caño Hondo to Santo Domingo Day 4 Salinas de Bani to Pedernales Day 5 Cabo Rojo & Southern Sierra de Bahoruco Day 6 Cachote to Villa Barrancoli Day 7 Northern Sierra de Bahoruco Day 8 La Placa, Laguna Rincon to Santo Domingo Day 9 International Departures TOUR ROUTE MAP… RBL Dominican Republic Itinerary 3 THE TOUR IN DETAIL… Day 1: Arrival in Santo Domingo. -
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. -
Colecciones Zoológicas, Su Conservación Y Manejo II.Pdf
1 Programa Interés Nacional Uso sostenible de los componentes de la Diversidad Biológica en Cuba Agencia de Medio Ambiente Ministerio de Ciencia, Tecnología y Medio Ambiente INFORME FINAL DE PROYECTO Colecciones Zoológicas, su conservación y manejo II Instituto de Ecología y Sistemática La Habana 2017 2 Índice Datos generales 5 Personal vinculado al proyecto 5 Correspondencia entre los objetivos planteados y los resultados alcanzados 7 Objetivos 7 Salidas programadas 7 Resultados 8 Nivel de ejecución y análisis del presupuesto asignado 11 Correspondencia entre la relación costo-beneficio alcanzado y el previsto (impacto 12 científico, tecnológico, económico, social, y ambiental) Informe científico-técnico 13 Introducción 13 Materiales y métodos 14 Resultados y discusión 16 Incremento de la riqueza y representatividad en las colecciones. Catalogación 16 Incremento de las bases de datos Seguimiento de los procedimientos curatoriales 20 Inventario de colecciones zoológicas 30 Educación ambiental 30 Conclusiones 31 Recomendaciones 32 Referencias 32 Anexo I. Artículos científico-técnicos. 34 Anexo II. Cursos impartidos y recibidos. 45 Anexo III. Tesis. 48 Anexo IV. Eventos. 49 Anexo V. Inventario de las colecciones zoológicas 53 Anexo VI. Diagnósticos de estado técnico y planes de conservación y manejo de las 58 colecciones 3 VII. Educación ambiental. 159 *Adjunto en soporte digital (DC). Bases de Datos y Artículos Científico-Técnicos (PDF). 4 INFORME FINAL RESULTADOS DE PROYECTO Título del Proyecto: Colecciones Zoológicas, su conservación y manejo II. Código: P1211LH005-006 Duración: 2015-2017 Programa: Uso sostenible de los componentes de la Diversidad Biológica en Cuba. Clasificación: Investigación Básica Institución cabecera: Instituto de Ecología y Sistemática Investigador principal: MSc. -
<I>ANOLIS</I> LIZARDS in the FOOD WEBS of STRUCTURALLY
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2016 ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA Nathan W. Turnbough University of Tennessee, Knoxville, [email protected] Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Terrestrial and Aquatic Ecology Commons Recommended Citation Turnbough, Nathan W., "ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA. " PhD diss., University of Tennessee, 2016. https://trace.tennessee.edu/utk_graddiss/4174 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Nathan W. Turnbough entitled "ASSESSING THE FUNCTIONAL SIMILARITY OF NATIVE AND INVASIVE ANOLIS LIZARDS IN THE FOOD WEBS OF STRUCTURALLY-SIMPLE HABITATS IN FLORIDA." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Ecology and Evolutionary Biology. -
1919 Barbour the Herpetology of Cuba.Pdf
5 2^usniuc^££itt£j IK: Bofji^D ^Jae HARVARD UNIVERSITY. I LIBRARY OF THE MUSEUM OF COMPARATIVE ZOOLOGY GIFT OF jflDemoirs of tbe /IDuseum of Comparattve ZooloQ? AT HARVARD COLLEGE. Vol. XLVII. No. 2. THE HRKFETOLOGY OF CUBA. BY THOMAS BARBOUR AND CHARLES T. RAMSDEN. WITH FIFTEEN PLATES. CAMBRIDGE, U. S. A.: IPrlnteb for tbe jIDuseum, May, 1919. i /IDemotta of tbe /iDuseum of Comparattve Zoology AT HARVARD COLLEGE. Vol. XLVII. No. 2. (./,!', THE HERPETOLOGY OF CUBA. BY THOMAS BARBOUR AND CHARLES T. RAMSDEN. WITH FIFTEEN PLATES. CAMBRIDGE, U. S. A.: Iprtnteft for tbe /IDuseum. May, 1919. {^A CONTENTS. Page Page Introduction 73 Gonatodes fuscus (Hallowell), Synopsis of the species 73 Plate 1, fig. 5 114 Species erroneously recorded .... 75 Tarentola cubana (Gundlach & Geographic note 78 Peters), Plate 14, fig. 1 . 116 Faiinal relationships 79 Hemidactylus mabouia (Moreau Check list of the species 83 de Jonnes) 117 Systematic account of the species . 93 Key to the species of Sphaerodactylus 1 19 Keys 93 Sphaerodactylus torrei Barbour, Amphibia Salientia 93 Plate 2, fig. 1, 2 119 Key to the genera 93 elegans MacLea>', Plate 2, fig. 3 121 Hylidae 93 cinereus MacLeay, Plate 2, fig. 4 122 Hyla septentrionalis Boulenger, nigropunctatus Gray, Plate 3, 1 Plate 1, fig. 1 93 fig. 124 Bufonidae 95 notatus Baird, Plate 3, fig. 2 125 Key to the species of Bufo ... 95 *scaber Barbour & Ramsden Plate Bufo longinasus Stejneger, Plate 3, fig. 3 126 13, fig. 1 ....... 95 Iguanidae 128 ramsdeni Barbour, Plate 1, fig. 2 96 Chamaeleolis chamaeleontides peltacephalus Tschudi, Plate 13, (Dmneril & Bibron) Plate 14, fig. -
Nest Success of Southeastern American Kestrels Associated with Red-Cockaded Woodpeckers in Old-Growth Longleaf Pine Habitat in Northwest Florida
2004SOUTHEASTERN NATURALIST 3(2):191–204 Nest Success of Southeastern American Kestrels Associated with Red-Cockaded Woodpeckers in Old-Growth Longleaf Pine Habitat in Northwest Florida 1,* 2 1,3 KATHLEEN E. GAULT , JEFFREY R. WALTERS , JOSEPH TOMCHO, JR. , 1,4 1,5 LOUIS F. PHILLIPS, JR. , AND ANDREW BUTLER Abstract - The Southeastern American Kestrel (Falco sparverius paulus), a non-migratory subspecies of the widespread American Kestrel, has declined to the point that it is listed as threatened in Florida, the state in which it is most common. We studied the nesting biology of Southeastern American Kestrels in 1999 and 2000 at Eglin Air Force Base, FL, in old-growth longleaf pine sa- vanna, a habitat type historically widely occupied by the kestrels. Most of the nest cavities we observed were in old-growth trees, both living and dead, and were originally excavated by Red-cockaded Woodpeckers (Picoides borealis) and then enlarged by other woodpecker species. Nesting success was 70% in 1999 and 56% in 2000. In 1999, 67% of eggs survived to become fledglings in successful nests, as did 58% in 2000. Nests in live pines and snags were equally successful, and nest success was positively related to cavity height in 1999. Reduced nesting success in 2000 may have been related to severe drought conditions. High nesting concentrations of up to 4 pairs per km2 were observed. We suggest that stands of old-growth longleaf pine, with little or no hardwood midstory and a relatively high number of snags, inhabited by Red-cockaded Woodpeckers, may constitute high quality habitat for Southeastern American Kestrels. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Attacked from Above and Below, New Observations of Cooperative and Solitary Predators on Roosting Cave Bats
bioRxiv preprint doi: https://doi.org/10.1101/550582; this version posted February 17, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Attacked from above and below, new observations of cooperative and solitary predators on roosting cave bats Krizler Cejuela. Tanalgo1, 2, 3, 7*, Dave L. Waldien4, 5, 6, Norma Monfort6, Alice Catherine Hughes1, 3* 1Landscape Ecology Group, Centre for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China 2International College, University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China 3Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China 4Harrison Institute, Bowerwood House, 15 St Botolph’s Road, Sevenoaks, Kent, TN13 3AQ, United Kingdom 5Christopher Newport University, 1 Avenue of the Arts, Newport News, VA 23606, United States of America 6Philippine Bats for Peace Foundation Inc., 5 Ramona Townhomes, Guadalupe Village, Lanang, Davao City 7Department of Biological Sciences, College of Arts and Sciences, University of Southern Mindanao, Kabacan 9407, North Cotabato, the Republic of the Philippines Corresponding authors: ACH ([email protected]) and KCT ([email protected]) Landscape Ecology Group, Centre for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun, Mengla, Yunnan Province 666303, People’s Republic of China Abstract Predation of bats in their roosts has previously only been attributed to a limited number of species such as various raptors, owls, and snakes.