Care and Rehabilitation of Microbats
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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 ..................................................................................................................... -
Diversity and Abundance of Roadkilled Bats in the Brazilian Atlantic Forest
diversity Article Diversity and Abundance of Roadkilled Bats in the Brazilian Atlantic Forest Lucas Damásio 1,2 , Laís Amorim Ferreira 3, Vinícius Teixeira Pimenta 3, Greiciane Gaburro Paneto 4, Alexandre Rosa dos Santos 5, Albert David Ditchfield 3,6, Helena Godoy Bergallo 7 and Aureo Banhos 1,3,* 1 Centro de Ciências Exatas, Naturais e da Saúde, Departamento de Biologia, Universidade Federal do Espírito Santo, Alto Universitário, s/nº, Guararema, Alegre 29500-000, ES, Brazil; [email protected] 2 Programa de Pós-Graduação em Ecologia, Instituto de Ciências Biológicas, Campus Darcy Ribeiro, Universidade de Brasília, Brasília 70910-900, DF, Brazil 3 Programa de Pós-Graduação em Ciências Biológicas (Biologia Animal), Universidade Federal do Espírito Santo, Av. Fernando Ferrari, 514, Prédio Bárbara Weinberg, Vitória 29075-910, ES, Brazil; [email protected] (L.A.F.); [email protected] (V.T.P.); [email protected] (A.D.D.) 4 Centro de Ciências Exatas, Naturais e da Saúde, Departamento de Farmácia e Nutrição, Universidade Federal do Espírito Santo, Alto Universitário, s/nº, Guararema, Alegre 29500-000, ES, Brazil; [email protected] 5 Centro de Ciências Agrárias e Engenharias, Departamento de Engenharia Rural, Universidade Federal do Espírito Santo, Alto Universitário, s/nº, Guararema, Alegre 29500-000, ES, Brazil; [email protected] 6 Centro de Ciências Humanas e Naturais, Departamento de Ciências Biológicas, Universidade Federal do Espírito Santo, Av. Fernando Ferrari, 514, Vitória 29075-910, ES, Brazil 7 Departamento de Ecologia, Instituto de Biologia Roberto Alcântara Gomes, Universidade do Estado do Rio de Janeiro, Rua São Francisco Xavier 524, Maracanã, Rio de Janeiro 20550-900, RJ, Brazil; [email protected] Citation: Damásio, L.; Ferreira, L.A.; * Correspondence: [email protected] Pimenta, V.T.; Paneto, G.G.; dos Santos, A.R.; Ditchfield, A.D.; Abstract: Faunal mortality from roadkill has a negative impact on global biodiversity, and bats are Bergallo, H.G.; Banhos, A. -
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. -
Lasiurus Egregius (Peters, 1870) (Chiroptera, Vespertilionidae) in Paraná State, Southern Brazil
15 6 NOTES ON GEOGRAPHIC DISTRIBUTION Check List 15 (6): 1099–1105 https://doi.org/10.15560/15.6.1099 First record of Lasiurus egregius (Peters, 1870) (Chiroptera, Vespertilionidae) in Paraná state, southern Brazil Fernando Carvalho1, 2, Daniela Aparecida Savariz Bôlla3, Karolaine Porto Supi1, Luana da Silva Biz1, 2, Beatriz Fernandes Lima Luciano1, 2, 4, Jairo José Zocche2, 4 1 Universidade do Extremo Sul Catarinense, Laboratório de Zoologia e Ecologia de Vertebrados, Av. Universitária n.1105, Bairro Universitário, Criciúma, SC, CEP: 80806-000, Brazil. 2 Universidade do Extremo Sul Catarinense, Programa de Pós-Graduação em Ciências Ambientais, Av. Universitária n.1105, Bairro Universitário, Criciúma, SC, CEP: 80806-000, Brazil. 3 National Institute for Amazonian Research (INPA), Post Graduation Program in Ecology, Av. André Araújo, n.2936, Bairro Petrópolis, Manaus, AM, CEP: 69.067-375, Brazil. 4 Universidade do Extremo Sul Catarinense, Laboratório de Ecologia de Paisagem e de Vertebrados Av. Universitária n.1105, Bairro Universitário, Criciúma, SC, CEP: 80806-000, Brazil. Corresponding author: Fernando Carvalho e-mail: [email protected] Abstract Lasiurus egregius (Peters, 1870) is an insectivorous bat species known from Central and South America. This species has few confirmed records throughout its distribution. Here we report the first record of L. egregius from the northern coast of Paraná state, southern Brazil. We captured a female individual of L. egregius using an ultrathin mist-net installed over a river knee, at Salto Morato Natural Reserve, municipality of Guaraqueçaba. This is the fourteenth locality with confirmed occurrence of L. egregius, being eight of them in Brazil. The knowledge on the bat fauna in Paraná has been increasing in recent decades, mainly due to the new studies in coast areas of this state. -
17 Roberts Road, Eastern Creek
17 ROBERTS ROAD, EASTERN CREEK SSD-10330 Proposed Data Centre Biodiversity Development Assessment Report Prepared for: Canberra Data Centres Pty Ltd PO Box 304 JERRABOMBERRA NSW 2619 SLR Ref: 610.18883-R05 Version No: -v2.0 November 2019 Canberra Data Centres Pty Ltd SLR Ref No: 610.18883-R05-v2.0-Eastern Creek BDAR-20191111.docx 17 Roberts Road, Eastern Creek November 2019 SSD-10330 Proposed Data Centre Biodiversity Development Assessment Report PREPARED BY SLR Consulting Australia Pty Ltd ABN 29 001 584 612 10 Kings Road New Lambton NSW 2305 Australia (PO Box 447 New Lambton NSW 2305 Australia) T: +61 2 4037 3200 E: [email protected] www.slrconsulting.com BASIS OF REPORT This report has been prepared by SLR Consulting Australia Pty Ltd (SLR) with all reasonable skill, care and diligence, and taking account of the timescale and resources allocated to it by agreement with Canberra Data Centres Pty Ltd (the Client). Information reported herein is based on the interpretation of data collected, which has been accepted in good faith as being accurate and valid. This report is for the exclusive use of the Client. No warranties or guarantees are expressed or should be inferred by any third parties. This report may not be relied upon by other parties without written consent from SLR. SLR disclaims any responsibility to the Client and others in respect of any matters outside the agreed scope of the work. DOCUMENT CONTROL Reference Date Prepared Checked Authorised 610.18883-R05-v2.0 11 November 2019 Fiona Iolini and David Martin Jeremy -
Southern Gulf, Queensland
Biodiversity Summary for NRM Regions Species List What is the summary for and where does it come from? This list has been produced by the Department of Sustainability, Environment, Water, Population and Communities (SEWPC) for the Natural Resource Management Spatial Information System. The list was produced using the AustralianAustralian Natural Natural Heritage Heritage Assessment Assessment Tool Tool (ANHAT), which analyses data from a range of plant and animal surveys and collections from across Australia to automatically generate a report for each NRM region. Data sources (Appendix 2) include national and state herbaria, museums, state governments, CSIRO, Birds Australia and a range of surveys conducted by or for DEWHA. For each family of plant and animal covered by ANHAT (Appendix 1), this document gives the number of species in the country and how many of them are found in the region. It also identifies species listed as Vulnerable, Critically Endangered, Endangered or Conservation Dependent under the EPBC Act. A biodiversity summary for this region is also available. For more information please see: www.environment.gov.au/heritage/anhat/index.html Limitations • ANHAT currently contains information on the distribution of over 30,000 Australian taxa. This includes all mammals, birds, reptiles, frogs and fish, 137 families of vascular plants (over 15,000 species) and a range of invertebrate groups. Groups notnot yet yet covered covered in inANHAT ANHAT are notnot included included in in the the list. list. • The data used come from authoritative sources, but they are not perfect. All species names have been confirmed as valid species names, but it is not possible to confirm all species locations. -
Myzopodidae: Chiroptera) from Western Madagascar
ARTICLE IN PRESS www.elsevier.de/mambio Original investigation The description of a new species of Myzopoda (Myzopodidae: Chiroptera) from western Madagascar By S.M. Goodman, F. Rakotondraparany and A. Kofoky Field Museum of Natural History, Chicago, USA and WWF, Antananarivo, De´partement de Biologie Animale, Universite´ d’Antananarivo, Antananarivo, Madagasikara Voakajy, Antananarivo, Madagascar Receipt of Ms. 6.2.2006 Acceptance of Ms. 2.8.2006 Abstract A new species of Myzopoda (Myzopodidae), an endemic family to Madagascar that was previously considered to be monospecific, is described. This new species, M. schliemanni, occurs in the dry western forests of the island and is notably different in pelage coloration, external measurements and cranial characters from M. aurita, the previously described species, from the humid eastern forests. Aspects of the biogeography of Myzopoda and its apparent close association with the plant Ravenala madagascariensis (Family Strelitziaceae) are discussed in light of possible speciation mechanisms that gave rise to eastern and western species. r 2006 Deutsche Gesellschaft fu¨r Sa¨ugetierkunde. Published by Elsevier GmbH. All rights reserved. Key words: Myzopoda, Madagascar, new species, biogeography Introduction Recent research on the mammal fauna of speciation molecular studies have been very Madagascar has and continues to reveal informative to resolve questions of species remarkable discoveries. A considerable num- limits (e.g., Olson et al. 2004; Yoder et al. ber of new small mammal and primate 2005). The bat fauna of the island is no species have been described in recent years exception – until a decade ago these animals (Goodman et al. 2003), and numerous remained largely under studied and ongoing other mammals, known to taxonomists, surveys and taxonomic work have revealed await formal description. -
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. -
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. -
Ecosystem Services Provided by Bats
Ann. N.Y. Acad. Sci. ISSN 0077-8923 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES Issue: The Year in Ecology and Conservation Biology Ecosystem services provided by bats Thomas H. Kunz,1 Elizabeth Braun de Torrez,1 Dana Bauer,2 Tatyana Lobova,3 and Theodore H. Fleming4 1Center for Ecology and Conservation Biology, Department of Biology, Boston University, Boston, Massachusetts. 2Department of Geography, Boston University, Boston, Massachusetts. 3Department of Biology, Old Dominion University, Norfolk, Virginia. 4Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona Address for correspondence: Thomas H. Kunz, Ph.D., Center for Ecology and Conservation Biology, Department of Biology, Boston University, Boston, MA 02215. [email protected] Ecosystem services are the benefits obtained from the environment that increase human well-being. Economic valuation is conducted by measuring the human welfare gains or losses that result from changes in the provision of ecosystem services. Bats have long been postulated to play important roles in arthropod suppression, seed dispersal, and pollination; however, only recently have these ecosystem services begun to be thoroughly evaluated. Here, we review the available literature on the ecological and economic impact of ecosystem services provided by bats. We describe dietary preferences, foraging behaviors, adaptations, and phylogenetic histories of insectivorous, frugivorous, and nectarivorous bats worldwide in the context of their respective ecosystem services. For each trophic ensemble, we discuss the consequences of these ecological interactions on both natural and agricultural systems. Throughout this review, we highlight the research needed to fully determine the ecosystem services in question. Finally, we provide a comprehensive overview of economic valuation of ecosystem services. -
Conservation Assessments for Five Forest Bat Species in the Eastern United States
United States Department of Agriculture Conservation Forest Service Assessments for Five General Technical Report NC-260 Technical Guide Forest Bat Species in the 2006 Eastern United States Front Cover: Illustrations by Fiona Reid, Ontario, Canada ©. Species from top: Pipistrellus subflavus, Myotis leibii, Myotis austroriparius, Myotis septentrionalis, Nycticeius humeralis. United States Department of Agriculture Conservation Forest Service Assessments for Five General Technical Report NC-260 Technical Guide Forest Bat Species in the 2006 Eastern United States Edited by Frank R. Thompson, III Thompson, Frank R., III, ed. 2006. Conservation assessments for five forest bat species in the Eastern United States. Gen. Tech. Rep. NC-260. St. Paul, MN: U.S. Department of Agriculture, Forest Service, North Central Research Station. 82 p. Assesses the status, distribution, conservation, and management considerations for five Regional Forester Sensitive Species of forest bats on national forests in the Eastern United States: eastern pipistrelle, evening bat, southeastern myotis, eastern small-footed myotis, and northern long-eared bat. Includes information on the taxonomy, description, life history, habitat distribution, status, and population biology of each species. KEY WORDS: conservation status, habitat use, life history, Myotis austroriparius (southeastern myotis), Myotis leibii (eastern small-footed myotis), Myotis septentrionalis (northern long-eared bat), Pipistrellus subflavus (eastern pipistrelle), Nycticeius humeralis (evening bat), Region 9, USDA Forest Service Disclaimer The U.S. Department of Agriculture (USDA) prohibits discrimination in all its programs and activities on the basis of race, color, national origin, age, disability, and where applicable, sex, marital status, familial status, parental status, religion, sexual orientation, genetic information, political beliefs, reprisal, or because all or part of an individual’s income is derived from any public assistance program. -
Lesser False Vampire Bat
# 409 SMALL MAMMAL MAIL 21 January 2017 LESSER FALSE VAMPIRE BAT Megaderma spasma in Odisha IUCN Red List: Global — LC (Csorba et al. 2008) National India — LC Roosting of Megaderma spasma in Gupteswar caves of Odisha Mammalia The Lesser False Vampire Bat Megaderma spasma [Class of Mammals] Linnaeus, 1758 is one among the five species of megadermatids Chiroptera found in the Old World tropics (Wilson & Reeder 2005) and widely [Order of Bats] distributed over South and Southeast Asian countries (Csorba et Megadermatidae al. 2008). The species is found in humid areas ranging from dense [Family of False Vampire Bats] tropical moist forests in South Asia (Molur et al. 2002) to lowland Megaderma spasma primary and secondary forests in Southeast Asia (Heaney et al. [Lesser False Vampire 1991). Bat] [Common Asian Ghost The diurnal roosts include caves, abandoned buildings, Bat] temples, lofts of thatched huts, tiled roofs, tree hollows and Species described by disused mines (Csorba et al. 2008) and recently reported below Linnaeus in 1758 water tank (Devkar & Upadhyay 2015). It lives in small colonies of single individual (Debata et al. 2013) to 30 individuals (Ellis 2015) which varies seasonally. Zoo’s Print Vol. 32 | No. 1 21 # 409 SMALL MAMMAL MAIL 21 January 2017 Global Distribution (Csorba et al. 2008): South Asia — Bangladesh, India, Sri Lanka. Southeast Asia — Sumatra, Java, Sulawesi, Halmahera, Indonesia, Borneo (Brunei, Indonesia and Malaysia), Philippines. Roosting locations of Megaderma spasma in Eastern Ghats, Odisha In India, it is predominantly known from the Western Ghats and northeastern India (Bates & Harrison 1997; Csorba et al. 2008) with sporadic records from West Bengal (Molur et al.