Bciissue22018.Pdf
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Lista Patron Mamiferos
NOMBRE EN ESPANOL NOMBRE CIENTIFICO NOMBRE EN INGLES ZARIGÜEYAS DIDELPHIDAE OPOSSUMS Zarigüeya Neotropical Didelphis marsupialis Common Opossum Zarigüeya Norteamericana Didelphis virginiana Virginia Opossum Zarigüeya Ocelada Philander opossum Gray Four-eyed Opossum Zarigüeya Acuática Chironectes minimus Water Opossum Zarigüeya Café Metachirus nudicaudatus Brown Four-eyed Opossum Zarigüeya Mexicana Marmosa mexicana Mexican Mouse Opossum Zarigüeya de la Mosquitia Micoureus alstoni Alston´s Mouse Opossum Zarigüeya Lanuda Caluromys derbianus Central American Woolly Opossum OSOS HORMIGUEROS MYRMECOPHAGIDAE ANTEATERS Hormiguero Gigante Myrmecophaga tridactyla Giant Anteater Tamandua Norteño Tamandua mexicana Northern Tamandua Hormiguero Sedoso Cyclopes didactylus Silky Anteater PEREZOSOS BRADYPODIDAE SLOTHS Perezoso Bigarfiado Choloepus hoffmanni Hoffmann’s Two-toed Sloth Perezoso Trigarfiado Bradypus variegatus Brown-throated Three-toed Sloth ARMADILLOS DASYPODIDAE ARMADILLOS Armadillo Centroamericano Cabassous centralis Northern Naked-tailed Armadillo Armadillo Común Dasypus novemcinctus Nine-banded Armadillo MUSARAÑAS SORICIDAE SHREWS Musaraña Americana Común Cryptotis parva Least Shrew MURCIELAGOS SAQUEROS EMBALLONURIDAE SAC-WINGED BATS Murciélago Narigudo Rhynchonycteris naso Proboscis Bat Bilistado Café Saccopteryx bilineata Greater White-lined Bat Bilistado Negruzco Saccopteryx leptura Lesser White-lined Bat Saquero Pelialborotado Centronycteris centralis Shaggy Bat Cariperro Mayor Peropteryx kappleri Greater Doglike Bat Cariperro Menor -
Bat Distribution Size Or Shape As Determinant of Viral Richness in African Bats
Bat Distribution Size or Shape as Determinant of Viral Richness in African Bats Gae¨l D. Maganga1,2., Mathieu Bourgarel1,3,4*., Peter Vallo5,6, Thierno D. Dallo7, Carine Ngoagouni8, Jan Felix Drexler7, Christian Drosten7, Emmanuel R. Nakoune´ 8, Eric M. Leroy1,9, Serge Morand3,10,11. 1 Centre International de Recherches Me´dicales de Franceville, Franceville, Gabon, 2 Institut National Supe´rieur d’Agronomie et de Biotechnologies (INSAB), Franceville, Gabon, 3 CIRAD, UPR AGIRs, Montpellier, France, 4 CIRAD, UPR AGIRs, Harare, Zimbabwe, 5 Institute of Vertebrate Biology, Academy of Sciences of the Czech Republic, Brno, Czech Republic, 6 Institute of Experimental Ecology, Ulm University, Ulm, Germany, 7 Institute of Virology, University of Bonn Medical Centre, Bonn, Germany, 8 Institut Pasteur de Bangui, Bangui, Re´publique Centrafricaine, 9 Institut de Recherche pour le De´veloppement, UMR 224 (MIVEGEC), IRD/CNRS/UM1, Montpellier, France, 10 Institut des Sciences de l’Evolution, CNRS-UM2, CC065, Universite´ de Montpellier 2, Montpellier, France, 11 Centre d’Infectiologie Christophe Me´rieux du Laos, Vientiane, Lao PDR Abstract The rising incidence of emerging infectious diseases (EID) is mostly linked to biodiversity loss, changes in habitat use and increasing habitat fragmentation. Bats are linked to a growing number of EID but few studies have explored the factors of viral richness in bats. These may have implications for role of bats as potential reservoirs. We investigated the determinants of viral richness in 15 species of African bats (8 Pteropodidae and 7 microchiroptera) in Central and West Africa for which we provide new information on virus infection and bat phylogeny. -
Terrestrial Vertebrate Fauna Survey for Anketell Point Rail Alignment and Port Projects
Terrestrial Vertebrate Fauna Survey for Anketell Point Rail Alignment and Port Projects Prepared for Australian Premium Iron Management Pty Ltd FINAL REPORT 26 July 2010 Terrestrial Vertebrate Fauna Survey for Anketell Point Rail Alignment and Port Projects Australian Premium Iron Management Pty Ltd Terrestrial Vertebrate Fauna Survey for Anketell Point Rail Alignment and Port Projects Final Report Prepared for Australian Premium Iron Management Pty Ltd by Phoenix Environmental Sciences Pty Ltd Authors: Greg Harewood, Karen Crews Reviewer: Melanie White, Stewart Ford Date: 26 July 2010 Submitted to: Michelle Carey © Phoenix Environmental Sciences Pty Ltd 2010. The use of this report is solely for the Client for the purpose in which it was prepared. Phoenix Environmental Sciences accepts no responsibility for use beyond this purpose. All rights are reserved and no part of this publication may be reproduced or copied in any form without the written permission of Phoenix Environmental Sciences or Australian Premium Iron Management. Phoenix Environmental Sciences Pty Ltd 1/511 Wanneroo Road BALCATTA WA 6914 P: 08 9345 1608 F: 08 6313 0680 E: [email protected] Project code: 925-AP-API-FAU Phoenix Environmental Sciences Pty Ltd ii Terrestrial Vertebrate Fauna Survey for Anketell Point Rail Alignment and Port Projects Australian Premium Iron Management Pty Ltd TABLE OF CONTENTS EXECUTIVE SUMMARY ..........................................................................................................................v 1.0 INTRODUCTION ......................................................................................................................... -
Mammals of Jordan
© Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Mammals of Jordan Z. AMR, M. ABU BAKER & L. RIFAI Abstract: A total of 78 species of mammals belonging to seven orders (Insectivora, Chiroptera, Carni- vora, Hyracoidea, Artiodactyla, Lagomorpha and Rodentia) have been recorded from Jordan. Bats and rodents represent the highest diversity of recorded species. Notes on systematics and ecology for the re- corded species were given. Key words: Mammals, Jordan, ecology, systematics, zoogeography, arid environment. Introduction In this account we list the surviving mammals of Jordan, including some reintro- The mammalian diversity of Jordan is duced species. remarkable considering its location at the meeting point of three different faunal ele- Table 1: Summary to the mammalian taxa occurring ments; the African, Oriental and Palaearc- in Jordan tic. This diversity is a combination of these Order No. of Families No. of Species elements in addition to the occurrence of Insectivora 2 5 few endemic forms. Jordan's location result- Chiroptera 8 24 ed in a huge faunal diversity compared to Carnivora 5 16 the surrounding countries. It shelters a huge Hyracoidea >1 1 assembly of mammals of different zoogeo- Artiodactyla 2 5 graphical affinities. Most remarkably, Jordan Lagomorpha 1 1 represents biogeographic boundaries for the Rodentia 7 26 extreme distribution limit of several African Total 26 78 (e.g. Procavia capensis and Rousettus aegypti- acus) and Palaearctic mammals (e. g. Eri- Order Insectivora naceus concolor, Sciurus anomalus, Apodemus Order Insectivora contains the most mystacinus, Lutra lutra and Meles meles). primitive placental mammals. A pointed snout and a small brain case characterises Our knowledge on the diversity and members of this order. -
Corynorhinus Townsendii): a Technical Conservation Assessment
Townsend’s Big-eared Bat (Corynorhinus townsendii): A Technical Conservation Assessment Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project October 25, 2006 Jeffery C. Gruver1 and Douglas A. Keinath2 with life cycle model by Dave McDonald3 and Takeshi Ise3 1Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada 2Wyoming Natural Diversity Database, Old Biochemistry Bldg, University of Wyoming, Laramie, WY 82070 3Department of Zoology and Physiology, University of Wyoming, P.O. Box 3166, Laramie, WY 82071 Peer Review Administered by Society for Conservation Biology Gruver, J.C. and D.A. Keinath (2006, October 25). Townsend’s Big-eared Bat (Corynorhinus townsendii): a technical conservation assessment. [Online]. USDA Forest Service, Rocky Mountain Region. Available: http:// www.fs.fed.us/r2/projects/scp/assessments/townsendsbigearedbat.pdf [date of access]. ACKNOWLEDGMENTS The authors would like to acknowledge the modeling expertise of Dr. Dave McDonald and Takeshi Ise, who constructed the life-cycle analysis. Additional thanks are extended to the staff of the Wyoming Natural Diversity Database for technical assistance with GIS and general support. Finally, we extend sincere thanks to Gary Patton for his editorial guidance and patience. AUTHORS’ BIOGRAPHIES Jeff Gruver, formerly with the Wyoming Natural Diversity Database, is currently a Ph.D. candidate in the Biological Sciences program at the University of Calgary where he is investigating the physiological ecology of bats in northern arid climates. He has been involved in bat research for over 8 years in the Pacific Northwest, the Rocky Mountains, and the Badlands of southern Alberta. He earned a B.S. in Economics (1993) from Penn State University and an M.S. -
2020 Special Issue
Journal Home page : www.jeb.co.in « E-mail : [email protected] Original Research Journal of Environmental Biology TM p-ISSN: 0254-8704 e-ISSN: 2394-0379 JEB CODEN: JEBIDP DOI : http://doi.org/10.22438/jeb/4(SI)/MS_1904 Plagiarism Detector Grammarly New records and present status of bat fauna in Mizoram, North-Eastern India C. Vanlalnghaka Department of Zoology, Govt. Serchhip College, Mizoram–796 181, India *Corresponding Author Email : [email protected] Paper received: 08.12.2019 Revised received: 24.06.2020 Accepted: 10.07.2020 Abstract Aim: The present study aimed to investigate the diversity of bat fauna in Mizoram and prepare a checklist for future references. This study also investigated threats and suggested recommendations for implementing conservation measures for bat fauna in Mizoram. Methodology: The present study was carried out in different parts of Mizoram between January 2012 - October 2019. Bats were trapped by using mist nets and hoop nets. Diagnostic morphological characters of bat were used for species identification. Digital camera and video camera were also used for further identification and documentation of bats. Results: During January 2012 – December 2016, eighteen bat species were identified. Recently, from January 2017 - October 2019 insectivorous bat species, Scotomanes ornatus was first time documented in Serchhip District (23.3 ºN 92.83 ºE), Mizoram. In total nineteen bat species were identified in this study, out of which ten species were first time recorded and nine species were rediscovered from the previous documentation. From the previous and present data, total of thirty-six bat Study the diversity of bat fauna and prepared checklist in species were recorded in Mizoram- nine Mizoram. -
Id & Ecology of OC Bats by Stephanie Remington V2
Bats Found in Orange County by Stephanie Remington FOOD HABITAT ROOST* MIGRATION / HIBERNATION STATUS NOTES Family Phyllostomidae nose ornamentation (leaf); migratory (do not hibernate) (Leaf-nosed bats) Mexican long-tongued near night-blooming cactae & caves, mines, bldgs fall migration to maternity roosts in has moved north to S. Cal. as habitat is lost in Mexico and as we plant more exotic batΨ Choeronycteris Nectar, pollen O agavae colonial (up to ~50) Mexico & Central America cactae & agavae; fall & winter records in S. Cal.; sensitive to disturbance mexicana Family Molossidae visible tail; migratory (usually do not hibernate); colonial; females form maternity colonies during the spring and summer months (Free-tailed bats) Mexican free-tailed bat variety of crevices; colonial (100s - migratory in parts of its range; appears one of the most common bats in OC; year-round activity, although reduced in winter; high altitudes C Tadarida brasiliensis agricultural pests 20 million) to overwinter in OC adapts well to urban environments; one pup born in Jun-July Pocketed free-tailed batΨ primarily large variable, from desert scrub to crevices of rugged cliffs; considered resident in San Diego very similar to the Mexican free-tailed bat, but slightly larger and with ears connected at Nyctinomops O moths pine-oak forest colonial County; status unknown in OC the midline; single pup, born in late Jun-Jul femorosaccus Big free-tailed batΨ almost entirely large usu crevices in cliffs; known only from a couple of records in OC; intermediate in size between pocketed free- rugged, rocky habitats seasonal migrant O Nyctinomops macrotis moths colonial tail and western mastiff bats; one pup, born late spring Western mastiff batΨ cliffs, occ. -
Anatomy and Histology of the Heart in Egyptian Fruit
Journal of Entomology and Zoology Studies 2016; 4(5): 50-56 E-ISSN: 2320-7078 P-ISSN: 2349-6800 JEZS 2016; 4(5): 50-56 Anatomy and histology of the heart in Egyptian © 2016 JEZS fruit bat (Rossetus aegyptiacus) Received: 09-09-2016 Accepted: 10-10-2016 Bahareh Alijani Bahareh Alijani and Farangis Ghassemi Department of Biology, Jahrom branch, Islamic Azad University, Abstract Jahrom, Iran This study was conducted to obtain more information about bats to help their conservation. Since 5 fruit Farangis Ghassemi bats, Rossetus aegyptiacus, weighing 123.04±0.08 g were captured using mist net. They were Department of Biology, Jahrom anesthetized and dissected in animal lab. The removed heart components were measured, fixed, and branch, Islamic Azad University, tissue processing was done. The prepared sections (5 µm) were subjected to Haematoxylin and Eosin Jahrom, Iran stain, and mounted by light microscope. Macroscopic and microscopic features of specimens were examined, and obtained data analyzed by ANOVA test. The results showed that heart was oval and closed in the transparent pericardium. The left and right side of heart were different significantly in volume and wall thickness of chambers. Heart was large and the heart ratio was 1.74%. Abundant fat cells, intercalated discs, and purkinje cells were observed. According to these results, heart in this species is similar to the other mammals and observed variation, duo to the high metabolism and energy requirements for flight. Keywords: Heart, muscle, bat, flight, histology 1. Introduction Bats are the only mammals that are able to fly [1]. Due to this feature, the variation in the [2, 3] morphology and physiology of their organs such as cardiovascular organs is expected Egyptian fruit bat (Rossetus aegyptiacus) belongs to order megachiroptera and it is the only megabat in Iran [4]. -
Bat Rabies and Other Lyssavirus Infections
Prepared by the USGS National Wildlife Health Center Bat Rabies and Other Lyssavirus Infections Circular 1329 U.S. Department of the Interior U.S. Geological Survey Front cover photo (D.G. Constantine) A Townsend’s big-eared bat. Bat Rabies and Other Lyssavirus Infections By Denny G. Constantine Edited by David S. Blehert Circular 1329 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Suzette M. Kimball, Acting Director U.S. Geological Survey, Reston, Virginia: 2009 For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment, visit http://www.usgs.gov or call 1–888–ASK–USGS For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod To order this and other USGS information products, visit http://store.usgs.gov Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted materials contained within this report. Suggested citation: Constantine, D.G., 2009, Bat rabies and other lyssavirus infections: Reston, Va., U.S. Geological Survey Circular 1329, 68 p. Library of Congress Cataloging-in-Publication Data Constantine, Denny G., 1925– Bat rabies and other lyssavirus infections / by Denny G. Constantine. p. cm. - - (Geological circular ; 1329) ISBN 978–1–4113–2259–2 1. -
Historical and Geographic Distribution in Honduras
Occasional Papers Museum of Texas Tech University Number 375 15 April 2021 Bats in time: Historical and Geographic Distribution in Honduras Manfredo A. Turcios-Casco, Richard K. LaVal, Don E. Wilson, and Hefer D. Ávila-Palma Abstract Bat records from Honduras reported herein are based on 11,163 individuals representing 113 species and eight families, recorded from 1860 to 2020. The Global Biodiversity Informa- tion Facility (GBIF) and published records were used to document the history of bat collecting in Honduras, and the number of species expected for the country and their relative abundance were estimated. Herein, the first checklist available for each department in Honduras is provided, as well as a discussion of the history of bat research in the country, including three peaks that oc- curred in 1967–69, 1983, and 2001. The geographic position of Honduras and the variety of its ecosystems combine to promote a diversity of bat species that are typical of regions to both the north and the south of Honduras. Despite the relatively large number of specimens known from the country, details of the distribution and natural history of each species remain understudied. Key words: Central America, Chiroptera, Honduras, natural history, relative abundance Resumen Los registros de murciélagos de Honduras que se describen en este documento se basan en 11,163 individuos que representan 113 especies y ocho familias, registrados desde 1860 hasta 2020. El Fondo de Información sobre Biodiversidad Global (GBIF) y los registros publicados se utilizaron para documentar la historia de la recolección de murciélagos en Honduras. Además se estimó el número de especies esperadas para el país y se describe la abundancia relativa de todas las especie. -
Life History Account for Pallid
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group PALLID BAT Antrozous pallidus Family: VESPERTILIONIDAE Order: CHIROPTERA Class: MAMMALIA M038 Written by: J. Harris Reviewed by: P. Brown Edited by: D. Alley, R. Duke DISTRIBUTION, ABUNDANCE, AND SEASONALlTY The pallid bat is a locally common species of low elevations in California. It occurs throughout California except for the high Sierra Nevada from Shasta to Kern cos., and the northwestern corner of the state from Del Norte and western Siskiyou cos. to northern Mendocino Co. A wide variety of habitats is occupied, including grasslands, shrublands, woodlands, and forests from sea level up through mixed conifer forests. The species is most common in open, dry habitats with rocky areas for roosting. A yearlong resident in most of the range. SPECIFIC HABITAT REQUIREMENTS Feeding: Takes a wide variety of insects and arachnids, including beetles, orthopterans, homopterans, moths, spiders, scorpions, solpugids, and Jerusalem crickets. The stout skull and dentition of this species allows it to take large, hard-shelled prey. Forages over open ground, usually 0.5-2.5 m (1.6-8 ft) above ground level. Foraging flight is slow and maneuverable with frequent dips, swoops, and short glides. Many prey are taken on the ground. Gleaning is frequently used, and a few prey are taken aerially. Can maneuver well on the ground. May carry large prey to a perch or night roost for consumption. Ingestion of fruit in one study (Howell 1980) was a result of feeding on frugivorous moths. Uses echolocation for obstacle avoidance; possibly utilizes prey-produced sounds while foraging. -
Index of Handbook of the Mammals of the World. Vol. 9. Bats
Index of Handbook of the Mammals of the World. Vol. 9. Bats A agnella, Kerivoula 901 Anchieta’s Bat 814 aquilus, Glischropus 763 Aba Leaf-nosed Bat 247 aladdin, Pipistrellus pipistrellus 771 Anchieta’s Broad-faced Fruit Bat 94 aquilus, Platyrrhinus 567 Aba Roundleaf Bat 247 alascensis, Myotis lucifugus 927 Anchieta’s Pipistrelle 814 Arabian Barbastelle 861 abae, Hipposideros 247 alaschanicus, Hypsugo 810 anchietae, Plerotes 94 Arabian Horseshoe Bat 296 abae, Rhinolophus fumigatus 290 Alashanian Pipistrelle 810 ancricola, Myotis 957 Arabian Mouse-tailed Bat 164, 170, 176 abbotti, Myotis hasseltii 970 alba, Ectophylla 466, 480, 569 Andaman Horseshoe Bat 314 Arabian Pipistrelle 810 abditum, Megaderma spasma 191 albatus, Myopterus daubentonii 663 Andaman Intermediate Horseshoe Arabian Trident Bat 229 Abo Bat 725, 832 Alberico’s Broad-nosed Bat 565 Bat 321 Arabian Trident Leaf-nosed Bat 229 Abo Butterfly Bat 725, 832 albericoi, Platyrrhinus 565 andamanensis, Rhinolophus 321 arabica, Asellia 229 abramus, Pipistrellus 777 albescens, Myotis 940 Andean Fruit Bat 547 arabicus, Hypsugo 810 abrasus, Cynomops 604, 640 albicollis, Megaerops 64 Andersen’s Bare-backed Fruit Bat 109 arabicus, Rousettus aegyptiacus 87 Abruzzi’s Wrinkle-lipped Bat 645 albipinnis, Taphozous longimanus 353 Andersen’s Flying Fox 158 arabium, Rhinopoma cystops 176 Abyssinian Horseshoe Bat 290 albiventer, Nyctimene 36, 118 Andersen’s Fruit-eating Bat 578 Arafura Large-footed Bat 969 Acerodon albiventris, Noctilio 405, 411 Andersen’s Leaf-nosed Bat 254 Arata Yellow-shouldered Bat 543 Sulawesi 134 albofuscus, Scotoecus 762 Andersen’s Little Fruit-eating Bat 578 Arata-Thomas Yellow-shouldered Talaud 134 alboguttata, Glauconycteris 833 Andersen’s Naked-backed Fruit Bat 109 Bat 543 Acerodon 134 albus, Diclidurus 339, 367 Andersen’s Roundleaf Bat 254 aratathomasi, Sturnira 543 Acerodon mackloti (see A.