A Pocket Guide to the Bats of the Burnett Mary
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Bat Calls of New South Wales
Bat calls of New South Wales Region based guide to the echolocation calls of microchiropteran bats Michael Pennay1 , Brad Law2 & Linda Reinhold3 1 New South Wales Department of Environment and Conservation 2 State Forests of New South Wales 3 Queensland Department of Natural Resources and Mines Bat calls of New South Wales Bat calls of New South Wales Published by the NSW Department of Environment and Conservation May 2004 Copyright © NSW Department of Environment and Conservation ISBN 0 7313 6786 3 This guide is the result of a co-operative project between NSW National Parks and Wildlife Service, now the NSW Department of Environment and Conservation (DEC) and State Forests of NSW (SFNSW). DEC provided project funding, management, staff, reference calls, preparation and printing. SFNSW provided part funding and granted support of staff time and expertise, reference calls and editing. Research was conducted under NPWS scientific licence number A2753 and SFNSW special purpose permit for research number 05466. Material presented in this publication may be copied for personal use or republished for non-commercial purposes provided that NSW Department of Environment and Conservation is fully acknowledged as the copyright owner. Apart from these purposes or for private study, research, criticism or review, as permitted under the Australian Copyright Act, no part of this publication may be reproduced by any process without written permission from NSW Department of Environment and Conservation. Inquiries should be addressed to the NSW Department of Environment and Conservation. This publication should be cited as follows: Pennay, M., Law, B., Reinhold, L. (2004). Bat calls of New South Wales: Region based guide to the echolocation calls of Microchiropteran bats. -
Bat Conservation 2021
Bat Conservation Global evidence for the effects of interventions 2021 Edition Anna Berthinussen, Olivia C. Richardson & John D. Altringham Conservation Evidence Series Synopses 2 © 2021 William J. Sutherland This document should be cited as: Berthinussen, A., Richardson O.C. and Altringham J.D. (2021) Bat Conservation: Global Evidence for the Effects of Interventions. Conservation Evidence Series Synopses. University of Cambridge, Cambridge, UK. Cover image: Leucistic lesser horseshoe bat Rhinolophus hipposideros hibernating in a former water mill, Wales, UK. Credit: Thomas Kitching Digital material and resources associated with this synopsis are available at https://www.conservationevidence.com/ 3 Contents Advisory Board.................................................................................... 11 About the authors ............................................................................... 12 Acknowledgements ............................................................................. 13 1. About this book ........................................................... 14 1.1 The Conservation Evidence project ................................................................................. 14 1.2 The purpose of Conservation Evidence synopses ............................................................ 14 1.3 Who this synopsis is for ................................................................................................... 15 1.4 Background ..................................................................................................................... -
Living with Wildlife - Flying Foxes Fact Sheet No
LIVING WITH WILDLIFE - FLYING FOXES FACT SHEET NO. 0063 Living with wildlife - Flying Foxes What are flying foxes? flying foxes use to mark their territory and to attract females during the mating season. Flying foxes, also known as fruit bats, are winged mammals belonging to the sub-order group of megabats. Unlike the smaller insectivorous microbats, the Do flying foxes carry diseases? animal navigates using their eye sight and smell, as opposed to echolocation, Like most wildlife and pets, flying foxes may carry diseases that can affect and feed on nectar, pollen and fruit. Flying foxes forage from over 100 humans. Australian Bat Lyssavirus can be transmitted directly from flying species of native plants and may supplement this diet with introduced plants foxes to humans. The risk of contracting Lyssavirus is extremely low, with found in gardens, orchards and urban areas. transmission only possible through direct contact of saliva from an infected Of the four species of flying foxes native to mainland Australia, three reside animal with a skin penetrating bite or scratch. in the Gladstone Region. These species include the grey-headed flying fox Flying foxes are natural hosts of the Hendra virus, however, there is no (Pteropus poliocephalus), black flying fox (Pteropus alecto) and little red evidence that the virus can be transmitted directly to humans. It is believed flying fox (Pteropus scapulatus). that the virus is transmitted from flying foxes to horses through exposure to All of these species are protected under the Nature Conservation Act urine or birthing fluids. Vaccination is the most effective way of reducing the 1992 and the grey-headed flying fox is also listed as ‘vulnerable’ under the risk of the virus infecting horses. -
A Survey of the Bat Fauna
__________________________________________________________________________________ Assessment of risk to Large Forest Bat on Lord Howe Isand from proposed wind turbines. An assessment of the risk to the Large Forest Bat Vespadelus darlingtoni from proposed wind turbines on Lord Howe Island, New South Wales. A report to Lord Howe Island Board G.A. Hoye Fly By Night Bat Surveys Pty Ltd ABN 48 068 562 005 PO Box 271 BELMONT NSW 2280 Tel 4947 7794 Fax 4947 7537 January 2016 January 2016 Fly By Night Bat Surveys Pty Ltd __________________________________________________________________________________ 1 __________________________________________________________________________________ Assessment of risk to Large Forest Bat on Lord Howe Isand from proposed wind turbines. 1 INTRODUCTION Fly By Night Bat Surveys PL was requested by the Lord Howe Island Board to assess potential impacts to the Large Forest Bat from two proposed wind turbines to be sited in pasture on the southern flank of Transit Hill. This species is currently the only native mammal known to breed on the island. Previous survey has confirmed the presence of this species in the lower elevated parts of the island including the area where the two turbines are proposed (Fly By Night Bat Surveys 2010). A population of approximately 500 breeding females exists north of the airstrip, with a second smaller population centred around Mount Gower and Mount Lidgebird (Fly By Night Bat Surveys 2010-2014). Significant mortality of microchiropteran bats has occurred at utility wind farms in North America and Europe (eg Kunz 2007b). In eastern North America mortality from turbine strike along forested ridge tops varies from 15.3 to 41.1 bats per megawatt (MW) of installed capacity per year Kunz (2007b). -
Daytime Behaviour of the Grey-Headed Flying Fox Pteropus Poliocephalus Temminck (Pteropodidae: Megachiroptera) at an Autumn/Winter Roost
DAYTIME BEHAVIOUR OF THE GREY-HEADED FLYING FOX PTEROPUS POLIOCEPHALUS TEMMINCK (PTEROPODIDAE: MEGACHIROPTERA) AT AN AUTUMN/WINTER ROOST K.A. CONNELL, U. MUNRO AND F.R. TORPY Connell KA, Munro U and Torpy FR, 2006. Daytime behaviour of the grey-headed flying fox Pteropus poliocephalus Temminck (Pteropodidae: Megachiroptera) at an autumn/winter roost. Australian Mammalogy 28: 7-14. The grey-headed flying fox (Pteropus poliocephalus Temminck) is a threatened large fruit bat endemic to Australia. It roosts in large colonies in rainforest patches, mangroves, open forest, riparian woodland and, as native habitat is reduced, increasingly in vegetation within urban environments. The general biology, ecology and behaviour of this bat remain largely unknown, which makes it difficult to effectively monitor, protect and manage this species. The current study provides baseline information on the daytime behaviour of P. poliocephalus in an autumn/winter roost in urban Sydney, Australia, between April and August 2003. The most common daytime behaviours expressed by the flying foxes were sleeping (most common), grooming, mating/courtship, and wing spreading (least common). Behaviours differed significantly between times of day and seasons (autumn and winter). Active behaviours (i.e., grooming, mating/courtship, wing spreading) occurred mainly in the morning, while sleeping predominated in the afternoon. Mating/courtship and wing spreading were significantly higher in April (reproductive period) than in winter (non-reproductive period). Grooming was the only behaviour that showed no significant variation between sample periods. These results provide important baseline data for future comparative studies on the behaviours of flying foxes from urban and ‘natural’ camps, and the development of management strategies for this species. -
Pacific Sheath-Tailed Bat American Samoa Emballonura Semicaudata Semicaudata Species Report April 2020
Pacific Sheath-tailed Bat American Samoa Emballonura semicaudata semicaudata Species Report April 2020 U.S. Fish and Wildlife Service Pacific Islands Fish and Wildlife Office Honolulu, HI Cover Photo Credits Shawn Thomas, Bat Conservation International. Suggested Citation USFWS. 2020. Species Status Assessment for the Pacific Sheath Tailed Bat (Emballonura semicaudata semicaudata). April 2020 (Version 1.1). U.S. Fish and Wildlife Service, Pacific Islands Fish and Wildlife Office, Honolulu, HI. 57 pp. Primary Authors Version 1.1 of this document was prepared by Mari Reeves, Fred Amidon, and James Kwon of the Pacific Islands Fish and Wildlife Office, Honolulu, Hawaii. Preparation and review was conducted by Gregory Koob, Megan Laut, and Stephen E. Miller of the Pacific Islands Fish and Wildlife Office. Acknowledgements We thank the following individuals for their contribution to this work: Marcos Gorresen, Adam Miles, Jorge Palmeirim, Dave Waldien, Dick Watling, and Gary Wiles. ii Executive Summary This Species Report uses the best available scientific and commercial information to assess the status of the semicaudata subspecies of the Pacific sheath-tailed bat, Emballonura semicaudata semicaudata. This subspecies is found in southern Polynesia, eastern Melanesia, and Micronesia. Three additional subspecies of E. semicaudata (E.s. rotensis, E.s. palauensis, and E.s. sulcata) are not discussed here unless they are used to support assumptions about E.s. semicaudata, or to fill in data gaps in this analysis. The Pacific sheath-tailed bat is an Old-World bat in the family Emballonuridae, and is found in parts of Polynesia, eastern Melanesia, and Micronesia. It is the only insectivorous bat recorded from much of this area. -
Checklist of the Mammals of Indonesia
CHECKLIST OF THE MAMMALS OF INDONESIA Scientific, English, Indonesia Name and Distribution Area Table in Indonesia Including CITES, IUCN and Indonesian Category for Conservation i ii CHECKLIST OF THE MAMMALS OF INDONESIA Scientific, English, Indonesia Name and Distribution Area Table in Indonesia Including CITES, IUCN and Indonesian Category for Conservation By Ibnu Maryanto Maharadatunkamsi Anang Setiawan Achmadi Sigit Wiantoro Eko Sulistyadi Masaaki Yoneda Agustinus Suyanto Jito Sugardjito RESEARCH CENTER FOR BIOLOGY INDONESIAN INSTITUTE OF SCIENCES (LIPI) iii © 2019 RESEARCH CENTER FOR BIOLOGY, INDONESIAN INSTITUTE OF SCIENCES (LIPI) Cataloging in Publication Data. CHECKLIST OF THE MAMMALS OF INDONESIA: Scientific, English, Indonesia Name and Distribution Area Table in Indonesia Including CITES, IUCN and Indonesian Category for Conservation/ Ibnu Maryanto, Maharadatunkamsi, Anang Setiawan Achmadi, Sigit Wiantoro, Eko Sulistyadi, Masaaki Yoneda, Agustinus Suyanto, & Jito Sugardjito. ix+ 66 pp; 21 x 29,7 cm ISBN: 978-979-579-108-9 1. Checklist of mammals 2. Indonesia Cover Desain : Eko Harsono Photo : I. Maryanto Third Edition : December 2019 Published by: RESEARCH CENTER FOR BIOLOGY, INDONESIAN INSTITUTE OF SCIENCES (LIPI). Jl Raya Jakarta-Bogor, Km 46, Cibinong, Bogor, Jawa Barat 16911 Telp: 021-87907604/87907636; Fax: 021-87907612 Email: [email protected] . iv PREFACE TO THIRD EDITION This book is a third edition of checklist of the Mammals of Indonesia. The new edition provides remarkable information in several ways compare to the first and second editions, the remarks column contain the abbreviation of the specific island distributions, synonym and specific location. Thus, in this edition we are also corrected the distribution of some species including some new additional species in accordance with the discovery of new species in Indonesia. -
Insights Into Australian Bat Lyssavirus in Insectivorous Bats of Western Australia
Tropical Medicine and Infectious Disease Article Insights into Australian Bat Lyssavirus in Insectivorous Bats of Western Australia Diana Prada 1,*, Victoria Boyd 2, Michelle Baker 2, Bethany Jackson 1,† and Mark O’Dea 1,† 1 School of Veterinary Medicine, Murdoch University, Perth, WA 6150, Australia; [email protected] (B.J.); [email protected] (M.O.) 2 Australian Animal Health Laboratory, CSIRO, Geelong, VIC 3220, Australia; [email protected] (V.B.); [email protected] (M.B.) * Correspondence: [email protected]; Tel.: +61-893607418 † These authors contributed equally. Received: 21 February 2019; Accepted: 7 March 2019; Published: 11 March 2019 Abstract: Australian bat lyssavirus (ABLV) is a known causative agent of neurological disease in bats, humans and horses. It has been isolated from four species of pteropid bats and a single microbat species (Saccolaimus flaviventris). To date, ABLV surveillance has primarily been passive, with active surveillance concentrating on eastern and northern Australian bat populations. As a result, there is scant regional ABLV information for large areas of the country. To better inform the local public health risks associated with human-bat interactions, this study describes the lyssavirus prevalence in microbat communities in the South West Botanical Province of Western Australia. We used targeted real-time PCR assays to detect viral RNA shedding in 839 oral swabs representing 12 species of microbats, which were sampled over two consecutive summers spanning 2016–2018. Additionally, we tested 649 serum samples via Luminex® assay for reactivity to lyssavirus antigens. Active lyssavirus infection was not detected in any of the samples. -
BATS of the Golfo Dulce Region, Costa Rica
MURCIÉLAGOS de la región del Golfo Dulce, Puntarenas, Costa Rica BATS of the Golfo Dulce Region, Costa Rica 1 Elène Haave-Audet1,2, Gloriana Chaverri3,4, Doris Audet2, Manuel Sánchez1, Andrew Whitworth1 1Osa Conservation, 2University of Alberta, 3Universidad de Costa Rica, 4Smithsonian Tropical Research Institute Photos: Doris Audet (DA), Joxerra Aihartza (JA), Gloriana Chaverri (GC), Sébastien Puechmaille (SP), Manuel Sánchez (MS). Map: Hellen Solís, Universidad de Costa Rica © Elène Haave-Audet [[email protected]] and other authors. Thanks to: Osa Conservation and the Bobolink Foundation. [fieldguides.fieldmuseum.org] [1209] version 1 11/2019 The Golfo Dulce region is comprised of old and secondary growth seasonally wet tropical forest. This guide includes representative species from all families encountered in the lowlands (< 400 masl), where ca. 75 species possibly occur. Species checklist for the region was compiled based on bat captures by the authors and from: Lista y distribución de murciélagos de Costa Rica. Rodríguez & Wilson (1999); The mammals of Central America and Southeast Mexico. Reid (2012). Taxonomy according to Simmons (2005). La región del Golfo Dulce está compuesta de bosque estacionalmente húmedo primario y secundario. Esta guía incluye especies representativas de las familias presentes en las tierras bajas de la región (< de 400 m.s.n.m), donde se puede encontrar c. 75 especies. La lista de especies fue preparada con base en capturas de los autores y desde: Lista y distribución de murciélagos de Costa Rica. Rodríguez -
Morphometrics of the Family Emballonuridae
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by DigitalCommons@University of Nebraska University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Papers in Natural Resources Natural Resources, School of September 1992 Morphometrics of the Family Emballonuridae Patricia W. Freeman University of Nebraska-Lincoln, [email protected] Cliff A. Lemen University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/natrespapers Part of the Natural Resources and Conservation Commons Freeman, Patricia W. and Lemen, Cliff A., "Morphometrics of the Family Emballonuridae" (1992). Papers in Natural Resources. 19. https://digitalcommons.unl.edu/natrespapers/19 This Article is brought to you for free and open access by the Natural Resources, School of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Natural Resources by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Published in Contributions to Mammalogy in honor of Karl F. Koopman (T.A. Griffiths and D. Klingener, Eds.), Bulletin of the American Museum of Natural History, No. 206, pp. 54–60. Copyright © 1992 American Museum of Natural History. Used by permission. American Museum of Natural History http://www.amnh.org/ Bulletin of the American Museum of Natural History http://library.amnh.org/pubs/bulletin.html R N\~)H, ISo. 206 : 5'4-*b lqq'L Morphometrics of the Family Emballonuridae PATRICIA W. FREEMAN1 AND CLIFF A. LEMEN2 ABSTRACT Morphometric analysis revealed three distinc- all other emballonurids. Phylogenetic studies also tive groups among the genera of emballonurids. separated Taphozous-Saccolaimus as distinctive Taphozous-Saccolaimus is a group distinctive in but included diclidurids among other New World size and shape, particularly cranially. -
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. -
Nest Boxes: Creating Homes for Urban Wildlife
Nest Boxes: Creating homes for urban wildlife Importance of Hollows Australia is home to over 350 species of land animals that depend on the hollows that form in old growth eucalyptus trees for shelter or reproduction. Hollows are formed through loss of limb, insect activity (like termites), decay and weathering. Suitable hollows taken a minimum of 80- 100 years and for larger animals it could be 150-250 years for a suitable hollow to form. Some of the many animals in Australia that rely on tree hollows include parrots, owls, kingfishers, ducks, possums, gliders, micro bats and even many reptiles, frogs and invertebrates. Within urban areas hollow bearing trees are found on public land (national parks, water ways, beach foreshore and streets) and on private land (front and back yards). Many hollow dependent species are in decline due to the widespread loss of hollow bearing trees. In urban areas hollows are removed for urban development (new houses, roads and factories) and for public safety reasons. Even if these trees are replanted, up to 100 years or more may pass before they begin to form hollows suitable for use by wildlife. If hollow dependent species are to continue to survive in urban and rural areas, urgent action is required to protect hollow bearing trees wherever possible. Nest boxes are needed in areas where hollows have already been lost. What are Nest Boxes? Nest boxes act as an artificial hollow that provide opportunities for hollow dependent fauna to survive in areas where their natural breeding habitat has been destroyed. Nest boxes are most useful in areas where hollows are lacking and other aspects of habitat are sufficient, such as food and water supply.