Bats of the SA Murray Region
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
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 ..................................................................................................................... -
Bat Echolocation Research a Handbook for Planning and Conducting Acoustic Studies Second Edition
Bat Echolocation Research A handbook for planning and conducting acoustic studies Second Edition Erin E. Fraser, Alexander Silvis, R. Mark Brigham, and Zenon J. Czenze EDITORS Bat Echolocation Research A handbook for planning and conducting acoustic studies Second Edition Editors Erin E. Fraser, Alexander Silvis, R. Mark Brigham, and Zenon J. Czenze Citation Fraser et al., eds. 2020. Bat Echolocation Research: A handbook for planning and conducting acoustic studies. Second Edition. Bat Conservation International. Austin, Texas, USA. Tucson, Arizona 2020 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License ii Table of Contents Table of Figures ....................................................................................................................................................................... vi Table of Tables ........................................................................................................................................................................ vii Contributing Authors .......................................................................................................................................................... viii Dedication…… .......................................................................................................................................................................... xi Foreword…….. .......................................................................................................................................................................... -
Is Bat Hair Morphology Exceptional?
Vespertilio 17: 171–183, 2014 ISSN 1213-6123 Is bat hair morphology exceptional? Britten D. SESSIONS1, Chanell E. Nielson2, John M. SOWA3, Wilford M. HESS4, Wesley “Skip” Skidmore5 & Bradley A. Carmack6 1 Patent Attorney, Zilka-Kotab, 1155 N. First Street Ste. 105, San Jose, CA 95112, U.S.A.; [email protected] 2 Department of English, Brigham Young University, Provo, UT 84602, U.S.A. 3 Department of Chemical Engineering, Brigham Young University, Provo, UT 84602, U.S.A. 4 Department of Plant and Wildlife Sciences, Brigham Young University, Provo, UT 84602, U.S.A. 5 Life Sciences Museum, Brigham Young University, Provo, UT 84602, U.S.A. 6 HR Professional, Sunnyvale, CA 94089, U.S.A. Abstract. Surface hair scale patterns from 19 bat species (families Vespertilionidae and Molossidae) from Utah were studied using scanning electron microscopy (SEM). Hair width, scale length, pattern, and position in relation to the long axis were used to characterize morphology within species, and fa- milies within the order Chiroptera. Previous studies indicate variations within families. Hair morphology results make it evident that large variations and similarities within the families can be seen visually and codified for the order. In the family Vespertilionidae, variations in hair morphology necessitated better terminology, including two new terms for morphology patterns. In the family Molossidae, distinctions between species, and possibly within the family, may be evident using SEM imaging to characterize morphology characteristics, although only two species were studied in this family. More precise morpho- logical measurements than used for this study may be necessary to construct useful keys for species within at least some families of bat. -
Summer Indiana Bat Ecology in the Southern Appalachians
SUMMER INDIANA BAT ECOLOGY IN THE SOUTHERN APPALACHIANS: AN INVESTIGATION OF THERMOREGULATION STRATEGIES AND LANDSCAPE SCALE ROOST SELECTION _______________________ A thesis Presented to The College of Graduate and Professional Studies Department of Biology Indiana State University Terre Haute, Indiana ______________________ In Partial Fulfillment of the Requirements for the Degree Master’s in Biology _______________________ by Kristina Hammond August 2013 Kristina Hammond 2013 Keywords: Myotis sodalis, Indiana bat, thermoregulation, MaxENT, landscape, roosting ecology ii COMMITTEE MEMBERS Committee Chair: Joy O’Keefe, PhD Assistant Professor of Biology Indiana State University Committee Member: George Bakken, PhD Professor of Biology Indiana State University Committee Member: Stephen Aldrich, PhD Assistant Professor of Geography Indiana State University Committee Member: Susan Loeb, PhD Research Ecologist USDA Forest Service, Southern Research Station & Clemson University iii ABSTRACT In the southern Appalachians there are few data on the roost ecology of the federally endangered Indiana bat (Myotis sodalis). During 2008-2012, we investigated roosting ecology of the Indiana bat in ~280,000 ha in the Great Smoky Mountains National Park, Cherokee National Forest, and Nantahala National Forest in the southern Appalachians Mountains of Tennessee and North Carolina. We investigated 2 aspects of the Indiana bat’s roosting ecology: thermoregulation and the extrinsic factors that influence body temperature, and landscape-scale roost selection. To investigate thermoregulation of bats at roost, we used data gathered in 2012 from 6 female Indiana bats (5 adults and 1 juvenile) to examine how reproductive condition, group size, roost characteristics, air temperature, and barometric pressure related to body temperature of roosting bats. We found that air temperature was the primary factor correlated with bats’ body temperatures while at roost (P < 0.01), with few differences detected among reproductive classes in terms of thermoregulatory strategies. -
Are Megabats Flying Primates? Contrary Evidence from a Mitochondrial DNA Sequence
Aust. J. Bioi. Sci., 1988, 41, 327-32 Are Megabats Flying Primates? Contrary Evidence from a Mitochondrial DNA Sequence S. Bennett,A L. J. Alexander,A R. H. CrozierB,c and A. G. MackinlayA,c A School of Biochemistry, University of New South Wales, P.O. Box 1, Kensington, N.S.W. 2033. B School of Biological Science, University of New South Wales, P.O. Box 1, Kensington, N.S.W. 2033. C To whom reprint requests should be addressed. Abstract Bats (Chiroptera) are divided into the suborders Megachiroptera (fruit bats, 'megabats') and Micro chiroptera (predominantly insectivores, 'microbats'). It had been found that megabats and primates share a connection system between the retina and the midbrain not seen in microbats or other eutherian mammals, and challenging but plausible hypotheses were made that (a) bats are diphyletic and (b) megabats are flying primates. We obtained two DNA sequences from the mitochondrion of the fruit bat Pteropus poliocephalus, and performed phylogenetic analyses using the bat sequences in conjunction with homologous Drosophila, mouse, cow and human sequences. Two trees stand out as significantly more likely than any other; neither of these links the bat and human as the closest sequences. These results cast considerable doubt on the hypothesis that megabats are particularly close to primates. Introduction Various phylogenetic schemes based on morphology have linked bats and primates, such as in McKenna's (1975) grandorder Archonta, which also includes the Dermoptera (flying lemurs) and Scandentia (tree shrews). Molecular systematists, using immunological comparisons and amino acid sequences, have found that bats are not placed particularly close to primates, and that they are not diphyletic (Cronin and Sarich 1980; Dene et al. -
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. -
“Microbats Are in My House”!
“MICROBATS ARE IN MY HOUSE”! Answers to frequently asked questions about microbats in houses. Bats are ancient animals that have been around for about 50 million years. Australia has six families of microbats containing 58 species. Because microbats are small, nocturnal animals most people are unaware of this native Australian mammal. They are specifically adapted for flying and can have a wing span measuring up to 25cm. These little mammals use both eyesight and echolocation to fly at night in When hollow trees are cut down entire search of food. Microbats are gentle mammals but families of bats are misplaced. Habitat may bite if they feel frightened, threatened loss can lead to regional extinctions of microbats. Photo: Louise Saunders or are injured. Please be mindful that they have very delicate finger bones in their wings. Photograph: In the veranda support beams; Nyctophilus “WHAT ABOUT MY HEALTH? DON’T THEY gouldi ~ Gould’s long-eared bat. Photo- © Dr Les Hall. A good location, happy bats and happy humans. CARRY DISEASE?” Microbats are not a threat to human health if you do not handle them, especially not with BARE hands. Only three species of microbat have been identified with Australian Bat Lyssavirus (ABLV). There have only been two fatal cases of Lyssavirus in Australia affecting humans, one in 1996 and one in 1998; the 1996 case was associated with a bite from a microbat to a wildlife carer. Since then all bat carers must have pre-exposure vaccinations to enable them to rescue and care for bats safely. ABLV is an extremely rare, but fatal disease. -
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. -
Brigalow Belt Bioregion – a Biodiversity Jewel
Brigalow Belt bioregion – a biodiversity jewel Brigalow habitat © Craig Eddie What is brigalow? including eucalypt and cypress pine forests and The term ‘brigalow’ is used simultaneously to refer to; woodlands, grasslands and other Acacia dominated the tree Acacia harpophylla; an ecological community ecosystems. dominated by this tree and often found in conjunction with other species such as belah, wilga and false Along the eastern boundary of the Brigalow Belt are sandalwood; and a broader region where this species scattered patches of semi-evergreen vine thickets with and ecological community are present. bright green canopy species that are highly visible among the more silvery brigalow communities. These The Brigalow Belt bioregion patches are a dry adapted form of rainforest, relics of a much wetter past. The Brigalow Belt bioregion is a large and complex area covering 36,400 000ha. The region is thus recognised What are the issues? by the Australian Government as a biodiversity hotspot. Nature conservation in the region has received increasing attention because of the rapid and extensive This hotspot contains some of the most threatened loss of habitat that has occurred. Since World War wildlife in the world, including populations of the II the Brigalow Belt bioregion has become a major endangered bridled nail-tail wallaby and the only agricultural and pastoral area. Broad-scale clearing for remaining wild population of the endangered northern agriculture and unsustainable grazing has fragmented hairy-nosed wombat. The area contains important the original vegetation in the past, particularly on habitat for rare and threatened species including the, lowland areas. glossy black-cockatoo, bulloak jewel butterfl y, brigalow scaly-foot, red goshawk, little pied bat, golden-tailed geckos and threatened community of semi evergreen Biodiversity hotspots are areas that support vine thickets. -
ABLV Bat Stats June 2016
ABLV BAT STATS Australian Bat Lyssavirus Report - June 2016 Cases of ABLV infection - January to June 2016 Nine cases of Australian bat lyssavirus (ABLV) Table 1: ABLV infection in Australian bats as confirmed by infection were reported in bats in Australia between FAT, PCR, IHC and/or virus isolation^ January and June 2016, from Queensland, New South Wales and Victoria (Table 1). YEAR NSW NT QLD VIC WA SA Total Queensland 1995 0 0 1# 0 0 0 1 Two black flying-foxes (Pteropus alecto), two little red 1996 1 0 9 1 0 0 11 flying-foxes (P. scapulatus) and one spectacled flying-fox (P. conspicillatus) from Queensland were found to be 1997 7 1 27+ 0 0 0 35 infected with ABLV to June 2016. In three bats, behaviour 1998 1 0 26+ 0 0 0 27 changes and neurological signs were reported such as hanging low in a tree, agitation, being subdued and easy 1999 0 0 6 0 0 0 6 to handle, twitching, nystagmus, paresis and inability to hang. Increased respiratory rate and effort were 2000 1 0 14 0 0 0 15 additionally reported in one bat. One bat was submitted 2001 0 0 9 1 4 0 14 because a person was bitten when picking the bat up, and the other due to contact with a pet dog. 2002 4 0 10 2 1 0 17 Histopathological findings included mild to severe non- 2003 6 0 3 2 0 0 11 suppurative meningoencephalitis, ganglioneuritis, subacute aspiration pneumonia and mild sialoadenitis. In 2004 5 0 6 1 0 0 12 one bat the urinary bladder was markedly distended with 2005 6 0 5 0 0 0 11 urine and the bladder wall was haemorrhagic. -
Bat Community Structure and Habitat Use Across Disturbance Regimes
Bat community structure and habitat use across logging regimes in jarrah eucalypt forests of south-western Australia Paul W. Webala School of Biological Sciences Faculty of Sustainability, Environment and Life Sciences Murdoch University, Perth, Western Australia Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy August 2010 i Abstract In many parts of the world, the increasing demand for timber and other forest products has led to loss, fragmentation, degradation or modification of natural forest habitats. The consequences of such habitat changes have been well studied for some animal groups, however not much is known of their effects on bats. In Australia, logging of native forests is a major threat to the continent‘s biodiversity and while logging practices have undergone great changes in the past three decades to selective logging (including ecologically sustainable forest management), which is more sympathetic to wildlife, there is still concern about the effects of logging on the habitat of many forest-dwelling animals. The goal of this thesis was to investigate the effects of logging on the bat species assemblages at both community and individual species levels in terms of their foraging and roosting ecology in jarrah forests of south-western Australia. This information is necessary to strengthen the scientific basis for ecologically sustainable forest management in production forests. The outcome of this research may help in the formulation of policy and management decisions to ensure the long-term maintenance and survival of viable populations of forest-dwelling bats in these altered environments. Bats were selected because they comprise more than 25% of Australia‘s mammal species and constitute a major component of Australia‘s biodiversity. -
Bats of the YUS Conservation Area Papua New Guinea
Bats of the YUS Conservation Area Papua New Guinea Simon KA Robson1, 1 Tamara E Inkster & 2 Andrew K Krockenberger 1Centre for Tropical Biodiversity & Climate Change 2Centre for Tropical Environmental & Sustainability Science School of Marine & Tropical Biology James Cook University, Australia © 2012 Table of Contents Executive summary 5 Introduction and rationale 5 Methodology 6 Survey effort 6 Acoustic monitoring 6 Monitoring via mist nets and harp traps 8 Microbats of YUS 9 The role of acoustic monitoring in bat surveys 14 Species accounts 16 Aselliscus triscupidatus: Trident Leaf-nosed Bat 17 Hipposideros cervinus: Fawn Leaf-nosed Bat 19 Hipposiders diadema: Diadem Leaf-nosed Bat 21 Hipposideros maggietaylorae: Maggie Taylor’s Leaf-nosed Bat 23 Rhinolophus euryotis: New Guinea Horseshoe Bat 25 Rhinolophus megaphyllus: Eastern Horseshoe Bat 27 Pipistrellus collinus: Montain Pipistrelle 29 Murina florium: Insectivorous Tube-nosed Bat 31 Nyctophlus microtus: Papuan Big-eared Bat 33 Kerivouls muscina: Fly River Woolly Bat 35 Mosia nigrescens: Lesser Sheath-tailed Bat 37 cf35 38 cffm46 39 fm12 40 fm52 41 fm55 42 sfm9 43 sfm14 44 sfm22 45 sfm42 46 sfm45 47 sfm55 48 Macroglossus minimus nanus: Least Blossom Bat 49 Nyctimine albiventer: Common Tube-nosed Bat 51 Paranyctimene raptor: Green Tube-nosed-Bat 53 Syconycteris australis: Common Blossom Bat 55 Acknowledgements 57 References 57 Executive Summary This project provides the first description of and harp traps) and more recently developed bat community structure across a complete altitudinal