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Further Assessment of the Genus Neodon and the Description of a New Species from Nepal
RESEARCH ARTICLE Further assessment of the Genus Neodon and the description of a new species from Nepal 1³ 2 2 3 Nelish PradhanID , Ajay N. Sharma , Adarsh M. Sherchan , Saurav Chhetri , 4 1³ Paliza Shrestha , C. William KilpatrickID * 1 Department of Biology, University of Vermont, Burlington, Vermont, United States of America, 2 Center for Molecular Dynamics±Nepal, Kathmandu, Nepal, 3 Department of Biology, Trinity University, San Antonio, Texas, United States of America, 4 Department of Plant and Soil Science, University of Vermont, Burlington, Vermont, United States of America a1111111111 ³ These authors are joint senior authors on this work. a1111111111 * [email protected] a1111111111 a1111111111 a1111111111 Abstract Recent molecular systematic studies of arvicoline voles of the genera Neodon, Lasiopod- omys, Phaiomys, and Microtus from Central Asia suggest the inclusion of Phaiomys leu- OPEN ACCESS curus, Microtus clarkei, and Lasiopodomys fuscus into Neodon and moving Neodon juldaschi into Microtus (Blanfordimys). In addition, three new species of Neodon (N. linz- Citation: Pradhan N, Sharma AN, Sherchan AM, Chhetri S, Shrestha P, Kilpatrick CW (2019) Further hiensis, N. medogensis, and N. nyalamensis) have recently been described from Tibet. assessment of the Genus Neodon and the Analyses of concatenated mitochondrial (Cytb, COI) and nuclear (Ghr, Rbp3) genes recov- description of a new species from Nepal. PLoS ered Neodon as a well-supported monophyletic clade including all the recently described ONE 14(7): e0219157. https://doi.org/10.1371/ and relocated species. Kimura-2-parameter distance between Neodon from western Nepal journal.pone.0219157 compared to N. sikimensis (K2P = 13.1) and N. irene (K2P = 13.4) was equivalent to genetic Editor: Johan R. -
Tuesday, June
American Society of Mammalogists 87th Annual Meeting – Albuquerque UNM CAMPUS MAPS Hokona SUB CERIA Building MSB Alvarado Redondo Village. American Society of Mammalogists 87th Annual Meeting – Albuquerque UNM CAMPUS MAP DIRECTORY American Society of Mammalogists 87th Annual Meeting – Albuquerque UNM STUDENT UNION BUILDING MAP Plaza Level Theater Ballrooms A and B Technical Plenary, Members meetings, Mall Level Capstone, Technical (3rd) Vendor Upper Concourse Poster sessions, Refreshment Committee American Society of Mammalogists 87th Annual Meeting – Albuquerque ABREVIATED PROGRAM TUESDAY, JUNE 5TH Tuesday Board of Directors Dinner – University House 5:30pm WEDNESDAY – JUNE 6TH Wednesday Board of Directors, Continental Breakfast — Embassy (registration for board members) 8:00am Wed Board of Directors, Meeting — Embassy 9:00am-5:00pm Wed Registration and Dormitory Check-In — Student Union Building SUB Ballroom C 11:00am-6:00pm Wed Opening Social (host bar) 6:00pm-10:00pm & Continuing Registration and Check-in — SUB THURSDAY – JUNE 7TH Thursday Refreshments — SUB Upper Level (3rd floor) concourse 7:30am Thur Vendors — Lobo A & B SUB Upper Level (3rd floor) 7:30am-6:00pm Thur Welcome — SUB Ballroom A,B 8:10am Thur Plenary Session 1 — SUB Ballroom A,B 8:30-9:45am Thur Refreshment Break — SUB Upper Level (3rd floor) concourse 9:45am Technical Session 1 Technical Session 2 Technical Session 3 10:15am-12:15pm SUB Ballroom A SUB Ballroom B SUB Theater (Plaza Level 1st Floor) Behavior Genetics Biogeography Thur Lunch –On your own. Use meal plan (La Posada) or see packet for food choices. Committee meetings go to assigned room. 12:15pm Technical Session 4 Technical Session 5 Technical Session 6 Thur SUB Ballroom A SUB Ballroom B SUB Theater (Plaza Level 1st Floor) 1:45-3:45pm Behavior Physiology Systematics Thur Refreshment Break — SUB Upper Level (3rd floor) concourse 3:45pm Thur Symposium 1 - Long-term Studies of Small Mammal Communities in Arid and Semi-arid Ecosystems: Synthesis and Progress. -
Mammals from Upper Pleistocene of Afrânio, Pernambuco, Northeast of Brazil
Quaternary and Environmental Geosciences (2010) 02(2):01-11 Mamíferos do Pleistoceno Superior de Afrânio, Pernambuco, nordeste do Brasil Mammals from Upper Pleistocene of Afrânio, Pernambuco, northeast of Brazil Fabiana Marinho Silvaab, César Felipe Cordeiro Filgueirasac, Alcina Magnólia Franca Barretoad, Édison Vicente Oliveiraae a Universidade Federal de Pernambuco b c d e [email protected], [email protected], [email protected], [email protected] RESUMO Os mamíferos pleistocênicos são encontrados com frequência em toda a região Nordeste do Brasil. Os fósseis em geral ocorrem em tanques, lagoas, terraços fluviais, cavernas e ravinas. No estado de Pernambuco são registradas ocorrências de mamíferos pleistocênicos em 38 municípios. Neste trabalho, foram estudados aspectos taxonômicos e tafonômicos de paleofauna, preservada em lagoas da bacia do riacho Caboclo, tributário do rio São Francisco, em Afrânio, Pernambuco, Brasil. A pesquisa envolveu levantamento bibliográfico, cartográfico, trabalhos de campo e laboratoriais. Mais de 1.250 ossos, dentes e osteodermos foram estudados. A associação fossilífera é monotípica, poliespecífica, com os graus de fragmentação e desgaste variando em quatro classes. Os ossos foram preservados por conservação da composição química original, permineralização e substituição por calcita e por calcita magnesiana. Foi identificada uma diversificada fauna distribuída em cinco ordens (Tardigrada, Cingulata, Notoungulata, Proboscidea e Perissodactyla), sete famílias (Megatheriidae, Mylodontidae, Dasypodidae, Glyptodontidae, Toxodontidae, Gomphotheriidae e Equidae) com os taxa: Eremotherium laurillardi, Mylodonopsis ibseni, Panochthus greslebini, Holmesina paulacoutoi, Hoplophorus euphractus, Stegomastodon waringi, Toxodon platensis, equídeo e gliptodontideo indeterminados. Foram registrados pela primeira vez em Pernambuco os gêneros Hoplophorus e Mylodonopsis. A paleofauna é predominantemente herbívora, de um paleoambiente de savana ou cerrado. -
Mammalia, Cingulata, Glyptodontidae)
Rev. bras. paleontol. 15(1):113-122, Janeiro/Abril 2012 © 2012 by the Sociedade Brasileira de Paleontologia doi:10.4072/rbp.2012.1.10 REDESCRIPCIÓN Y DESIGNACIÓN DE UN NEOTIPO DE PANOCHTHUS TUBERCULATUS (OWEN) (MAMMALIA, CINGULATA, GLYPTODONTIDAE) MARTÍN ZAMORANO Departamento Científico de Paleontología de Vertebrados, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, CONICET, Paseo del Bosque s/n, 1900, La Plata. Argentina. [email protected] ÁLVARO MONES Franzensbadstraße 7b, 86199, Augsburg, Alemania. [email protected] GUSTAVO J. SCILLATO-YANÉ Departamento Científico de Paleontología de Vertebrados, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, CONICET, Paseo del Bosque s/n, 1900, La Plata, Argentina. [email protected] ABSTRACT – REDESCRIPTION AND DESIGNATION OF A NEOTYPE OF PANOCHTHUS TUBERCULATUS (OWEN) (MAMMALIA, CINGULATA, GLYPTODONTIDAE). We design a neotype for Panochthus tuberculatus (Owen), given that the holotype is missing. A diagnosis and detailed description of the neotype is provided. Glyptodon tuberculatus is the type species of Panochthus Burmeister, one of the genera of giant Pleistocene glyptodonts. P. tuberculatus is recorded in the Bonaerean (late middle Pleistocene) and Lujanian (thus far only for the late Pleistocene lapse of this age) of Argentina, Uruguay, Brazil, Paraguay and, with doubts, Bolivia. Firstly, the species was recognized on the basis of two fragments of dorsal armor; this type material (two syntypes) must be considered as lost, given that it has not been found in the collections of British Museum Natural History, where it was deposited. It is essential that material assigned to P. tuberculatus be made available, to establish the validity of each of the 19 species referred to this genus. -
Revisión Del Género Panochthus (Xenarthra, Glyptodontidae)
ISSN 0373-3823 UNIVERSIDAD NACIONAL DE LA PLATA - FACULTAD DE CIENCIAS NATURALES Y MUSEO Revista del Museo de La Plata 2014 Sección Paleontología, 14 (72): 1-46 Revisión del género Panochthus (Xenarthra, Glyptodontidae) M. Zamorano1,2, G. J. Scillato-Yané1,3 y A. E. Zurita4 1División Paleontología de Vertebrados, Museo de La Plata, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata. Paseo del Bosque s/n, 1900 La Plata. Argentina. CONICET. 2Cátedra de Zoología Vertebrados. E-mail: [email protected] 3Cátedra de Paleozoología. E-mail: [email protected] 4 Centro de Ecología Aplicada del Litoral (CECOAL-CONICET) y Universidad Nacional del Nordeste. Ruta 5, km. 2.5 (3400) Corrientes, Argentina. E-mail: [email protected] Correspondencia: Martín Zamorano. RESUMEN. Se revisa la totalidad de las especies del género Panochthus. Es uno de los gliptodóntidos más importantes del Pleistoceno de la Argentina por la frecuencia de sus registros en las unidades ensenadenses, bonaerenses y lujanenses, así como por su amplia distribución geográfica, que abarca desde la provincia de Santa Cruz hasta el norte argentino. También se extiende al Pleistoceno de Bolivia, Brasil, Paraguay, Perú y Uruguay. Hasta este momento se consideraban válidas un total de diez especies de Panochthus. En esta contribución se mantienen vigentes seis especies: (1) Panochthus tuberculatus (Owen), (2) P. frenzelianus Ameghino, (3) P. intermedius Lydekker, (4) P. subintermedius Castellanos, (5) P. greslebini Castellanos y (6) P. jaguaribensis Moreira. Se invalidan cuatro especies: (1) P. lundii Burmeister, por estar basada en material correspondiente a varias especies de gliptodóntidos ya conocidas; (2) P. -
Arvicolinae and Outgroup Mitochondrial Genome Accession Numbers
Supplementary Materials: Table S1: Arvicolinae and outgroup mitochondrial genome accession numbers. Species Name Accession Number Lasiopodomys brandtii MN614478.1 Lasiopodomys mandarinus JX014233.1 Lasiopodomys gregalis MN199169.1 Microtus fortis fortis JF261174.1 Microtus fortis calamorum JF261175.1 Microtus kikuchii AF348082.1 Neodon irene NC016055.1 Neodon fuscus MG833880.1 Neodon sikimensis KU891252.1 Microtus rossiaemeridionalis DQ015676.1 Microtus levis NC008064.1 Microtus arvalis MG948434.1 Terricola subterraneus MN326850.1 Microtus agrestis MH152570.1 Microtus richardsoni MT225016.1 Microtus ochrogaster KT166982.1 Proedromys liangshanensis FJ463038.1 Arvicola amphibius MN122828.1 Myodes regulus NC016427.1 Myodes rufocanus KT725595.1 Myodes rutilus MK482363.1 Myodes glareolus KF918859.1 Eothenomys melanogaster KP997311.1 Eothenomys miletus KX014874.1 Eothenomys chinensis FJ483847.1 Eothenomys Inez KU200225.1 Ondatra zibethicus KU177045.1 Dicrostonyx hudsonius KX683880.1 Dicrostonyx groenlandicus KX712239.1 Dicrostonyx torquatus MN792940.1 Prometheomys schaposchnikowi NC049036.1 Cricetulus griseus DQ390542.2 Peromyscus polionotus KY707301.1 Sigmodon hispidus KY707311.1 Mus musculus V00711.1 Table S2: Sequenced Wildwood Trust water vole samples. Sample Sample Enclosure Local ID Sex No. Type No. 1 Tissue TB31 - - 2 Tissue WW46 - - 3 Tissue WW0304/34 - Male 4 Tissue WW34/39 - - 5 Hair Q88 - Male 6 Hair Q100 - Male 7 Hair R95 - Male 8 Hair R12 - Male 9 Hair R28 - Male 10 Hair Q100 - Male 11 Faecal R2 2228 Male 12 Faecal Q52 2245 Female 13 Faecal Q42 2218 Female 14 Faecal Q7 2264 Female 15 Faecal Q75a 2326 Female 16 Faecal R50 2232 Male 17 Faecal R51 2225 Male 18 Faecal Q58 2314 Male 19 Faecal Q100 2185 Female 20 Faecal R27 2445 Female Table S3: Additional water vole sequences from previous publications. -
Occasional Papers Museum of Texas Tech University Number 265 21 December 2006
Occasional Papers Museum of Texas Tech University Number 265 21 December 2006 THE MAMMALS OF SAN ANGELO STATE PARK, TOM GREEN COUNTY, TEXAS JOEL G. BRANT, ROBERT C. DOWLER, AND CARLA E. EBELING ABSTRACT A survey of the mammalian fauna of San Angelo State Park, Tom Green County, Texas, began in April 1999 and includes data collected through November 2005. Thirty-one species of native mammals, representing 7 orders and 18 families, were verified at the state park. The mammalian fauna at the state park is composed primarily of western Edwards Plateau mam- mals, which include many Chihuahuan species, and mammals with widespread distributions. The most abundant species of small mammal at the state park were Neotoma micropus and Peromyscus maniculatus. The total trap success for this study (1.5%) was lower than expected and may reflect the drought conditions experienced in this area during the study period. Key words: Edwards Plateau, mammal survey, San Angelo State Park, Texas, Tom Green County, zoogeography INTRODUCTION San Angelo State Park (SASP) is located about tributaries, and the North Concho River with its asso- 10 km (6 mi.) west of San Angelo in Tom Green ciated tributaries and O. C. Fisher Reservoir (Fig. 1). County, Texas, and is situated around O. C. Fisher The North Concho River creates a dispersal corridor Reservoir and the North Concho River (Figs. 1 and for eastern species to move west into west-central 2). This area is an ecotonal zone at the junction of Texas. two major biotic regions in Texas, the Edwards Pla- teau (Balconian) to the south and the Rolling Plains to The soils of SASP are composed mostly of the north (Blair 1950). -
Exploring the Vastness of Banff National Park
Exploring the Vastness of Banff National Park By Claire Walter o borrow on old Ttravelogue cliché, Alberta’s Banff National Park is study in contrast. Its 2,586 square miles comprise both wilderness and civilization. There are high mountains, deep valleys, endless forests and abundant wildlife. Even though much of it feels and looks remote, it is just 70 miles from Calgary – and the Trans-Canada Highway runs right through it. It contains one large town (Banff), one smaller town (Lake Louise Village), two palatial hotels (the Fairmont Banff Springs and Fairmont Chateau Lake Louise) and three significant downhill ski areas (Ski Lake Louise, Sunshine and Norquay). It is a park among parks, with Kootenay National Park just to the south, Yoho National Park to the west (and in another province) and Jasper National Park to the north. It is Canada’s oldest national park and also the one with phenomenal snowshoe opportunities. It’s a great destination for a snowshoe getaway or a multi-activity winter vacation with snowshoeing among the options. There’s skiing (Alpine and Nordic), wildlife viewing, spa- hopping and enjoying the shops, galleries, restaurants and nightspots in Banff or quieter Lake 1 Go FartherTM Model: ARTICA™ BACKCOUNTRY q Two-Piece Articulating Frame q Virtual Pivot Traction Cam q Quick-Cinch™ One-Pull Binding q 80% Recyclable Materials, No PVC’s eastonmountainproducts.com ©2010 easton mountain products Louise Village. As a bonus, winter is low season in Banff, so lodging is a bargain and the shops offer incredible values. Snowshoeing Options The most straightforward snowshoeing is practically from the doorstep of the Chateau Lake Louise. -
Ther5 1 017 024 Golenishchev.Pm6
Russian J. Theriol. 5 (1): 1724 © RUSSIAN JOURNAL OF THERIOLOGY, 2006 The developmental conduit of the tribe Microtini (Rodentia, Arvicolinae): Systematic and evolutionary aspects Fedor N. Golenishchev & Vladimir G. Malikov ABSTRACT. According to the recent data on molecular genetics and comparative genomics of the grey voles of the tribe Microtini it is supposed, that their Nearctic and Palearctic groups had independently originated from different lineages of the extinct genus Mimomys. Nevertheless, that tribe is considered as a natural taxon. The American narrow-skulled voles are referred to a new taxon, Vocalomys subgen. nov. KEY WORDS: homology, homoplasy, phylogeny, vole, Microtini, evolution, taxonomy. Fedor N. Golenishchev [[email protected]] and Vladimir G. Malikov [[email protected]], Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, Saint-Petersburg 199034, Russia. «Êàíàë ðàçâèòèÿ» ïîëåâîê òðèáû Microtini (Rodentia, Arvicolinae): ñèñòåìàòèêî-ýâîëþöèîííûé àñïåêò. Ô.Í. Ãîëåíèùåâ, Â.Ã. Ìàëèêîâ ÐÅÇÞÌÅ.  ñîîòâåòñòâèè ñ ïîñëåäíèìè äàííûìè ìîëåêóëÿðíîé ãåíåòèêè è ñðàâíèòåëüíîé ãåíîìè- êè ñåðûõ ïîëåâîê òðèáû Microtini äåëàåòñÿ âûâîä î íåçàâèñèìîì ïðîèñõîæäåíèè íåàðêòè÷åñêèõ è ïàëåàðêòè÷åñêèõ ãðóïï îò ðàçíûõ ïðåäñòàâèòåëåé âûìåðøåãî ðîäà Mimomys. Íåñìîòðÿ íà ýòî, äàííàÿ òðèáà ñ÷èòàåòñÿ åñòåñòâåííûì òàêñîíîì. Àìåðèêàíñêèå óçêî÷åðåïíûå ïîëåâêè âûäåëÿþòñÿ â ñàìîñòîÿòåëüíûé ïîäðîä Vocalomys subgen. nov. ÊËÞ×ÅÂÛÅ ÑËÎÂÀ: ãîìîëîãèÿ, ãîìîïëàçèÿ, ôèëîãåíèÿ, ïîëåâêè, Microtini, ýâîëþöèÿ, òàêñîíîìèÿ. Introduction The history of the group in the light of The Holarctic subfamily Arvicolinae Gray, 1821 is the molecular data known to comprise a number of transberingian vicari- ants together with a few Holarctic forms. Originally, The grey voles are usually altogether regarded as a the extent of their phylogenetic relationships was judged first-hand descendant of the Early Pleistocene genus on their morphological similarity. -
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. -
Late Cenozoic Large Mammal and Tortoise Extinction in South America
Cione et al: Late Cenozoic extinction Rev.in South Mus. America Argentino Cienc. Nat., n.s.1 5(1): 000, 2003 Buenos Aires. ISSN 1514-5158 The Broken Zig-Zag: Late Cenozoic large mammal and tortoise extinction in South America Alberto L. CIONE1, Eduardo P. TONNI1, 2 & Leopoldo SOIBELZON1 1Departamento Científico Paleontología de Vertebrados, 'acultad de Ciencias Naturales y Museo, Paseo del Bosque, 1900 La Plata, Argentina. 2Laboratorio de Tritio y Radiocarbono, LATYR. 'acultad de Ciencias Naturales y Museo, Paseo del Bosque, 1900 La Plata, Argentina. E-mail: [email protected], [email protected], [email protected]. Corresponding author: Alberto L. CIONE Abstract: During the latest Pleistocene-earliest Holocene, South American terrestrial vertebrate faunas suffered one of the largest (and probably the youngest) extinction in the world for this lapse. Megamammals, most of the large mammals and a giant terrestrial tortoise became extinct in the continent, and several complete ecological guilds and their predators disappeared. This mammal extinction had been attributed mainly to overkill, climatic change or a combination of both. We agree with the idea that human overhunting was the main cause of the extinction in South America. However, according to our interpretation, the slaughtering of mammals was accom- plished in a particular climatic, ecological and biogeographical frame. During most of the middle and late Pleis- tocene, dry and cold climate and open areas predominated in South America. Nearly all of those megamammals and large mammals that became extinct were adapted to this kind of environments. The periodic, though rela- tively short, interglacial increases in temperature and humidity may have provoked the dramatic shrinking of open areas and extreme reduction of the biomass (albeit not in diversity) of mammals adapted to open habitats. -
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.