Bats of the YUS Conservation Area Papua New Guinea
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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 ..................................................................................................................... -
Morphometrical Variations of Malaysian Hipposideros Species
Malaysian Journal of Mathematical Sciences 6(1): 47-57 (2012) Morphometrical Variations of Malaysian Hipposideros Species Siti Nurlydia Sazali, Charlie J. Laman and M.T. Abdullah Department of Zoology, Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, 94300 Kota Samarahan, Sarawak, Malaysia E-mail: [email protected] ABSTRACT A study on the morphometrical variations among four Malaysian Hipposideros species was conducted using voucher specimens deposited in Universiti Malaysia Sarawak (UNIMAS) Zoological Museum and the Department of Widlife and National Park (DWNP) Kuala Lumpur. Twenty two individuals from four species of Hipposideros ater , H. bicolor , H. cineraceus and H. dyacorum were morphologically measured, in which a total of 27 linear parameters of body, skull and dentals of each were appropriately recorded. The statistical data were later subjected to discriminant function analysis (DFA) and canonical variate analysis (CVA) using SPSS version 15.0 and unweighted pair-group method average (UPGMA) cluster analysis using Minitab version 14.4. The highest character loadings observed in Function l, Function 2 and Function 3 were the forearm length (FA), the third digit second phalanx length (D3P2L) and the palatal length (PL) with standardised canonical discriminant function coefficient values of 21.910, 5.770 and 5.095, respectively. These three characters were identified as the best diagnostic features for discriminating these closely related species of Hipposideros . Hence, this morphometric approach could be a promising tool as an alternative to the molecular DNA analysis for identification of Chiroptera species. Keywords: Hipposideros , morphometric, discriminant function analysis cluster analysis, species identification. 1. INTRODUCTION Bats belong to the order Chiroptera and can be distinguished from all other mammals by their ability to fly, which is a result of the modification of their forelimbs into wings (Payne et al . -
Australasian Bat Society Newsletter
The Australasian Bat Society Newsletter Number 21 November 2003 ABS Website: http://abs.ausbats.org.au ABS Listserver: [email protected] ISSN 1448-5877 The Australasian Bat Society Newsletter, Number 21, Nov 2003 – Instructions for Contributors – The Australasian Bat Society Newsletter will accept contributions under one of the following two sections: Research Papers, and all other articles or notes. There are two deadlines each year: 31 st March for the April issue, and 31 st October for the November issue. The Editor reserves the right to hold over contributions for subsequent issues of the Newsletter , and meeting the deadline is not a guarantee of immediate publication. Opinions expressed in contributions to the Newsletter are the responsibility of the author, and do not necessarily reflect the views of the Australasian Bat Society, its Executive or members. For consistency, the following guidelines should be followed: • Emailed electronic copy of manuscripts or articles, sent as an attachment, is the preferred method of submission. Manuscripts can also be sent on 3½” floppy disk preferably in IBM format. Faxed and hard copy manuscripts will be accepted but reluctantly! Please send all submissions to the Newsletter Editor at the email or postal address below. • Electronic copy should be in 11 point Arial font, left and right justified with 16 mm left and right margins. Please use Microsoft Word; any version is acceptable. • Manuscripts should be submitted in clear, concise English and free from typographical and spelling errors. Please leave two spaces after each sentence. • Research Papers should include: Title; Names and addresses of authors; Abstract (approx. -
Molecular Phylogeny of Mobatviruses (Hantaviridae) in Myanmar and Vietnam
viruses Article Molecular Phylogeny of Mobatviruses (Hantaviridae) in Myanmar and Vietnam Satoru Arai 1, Fuka Kikuchi 1,2, Saw Bawm 3 , Nguyễn Trường Sơn 4,5, Kyaw San Lin 6, Vương Tân Tú 4,5, Keita Aoki 1,7, Kimiyuki Tsuchiya 8, Keiko Tanaka-Taya 1, Shigeru Morikawa 9, Kazunori Oishi 1 and Richard Yanagihara 10,* 1 Infectious Disease Surveillance Center, National Institute of Infectious Diseases, Tokyo 162-8640, Japan; [email protected] (S.A.); [email protected] (F.K.); [email protected] (K.A.); [email protected] (K.T.-T.); [email protected] (K.O.) 2 Department of Chemistry, Faculty of Science, Tokyo University of Science, Tokyo 162-8601, Japan 3 Department of Pharmacology and Parasitology, University of Veterinary Science, Yezin, Nay Pyi Taw 15013, Myanmar; [email protected] 4 Institute of Ecology and Biological Resources, Vietnam Academy of Science and Technology, Hanoi, Vietnam; [email protected] (N.T.S.); [email protected] (V.T.T.) 5 Graduate University of Science and Technology, Vietnam Academy of Science and Technology, Hanoi, Vietnam 6 Department of Aquaculture and Aquatic Disease, University of Veterinary Science, Yezin, Nay Pyi Taw 15013, Myanmar; [email protected] 7 Department of Liberal Arts, Faculty of Science, Tokyo University of Science, Tokyo 162-8601, Japan 8 Laboratory of Bioresources, Applied Biology Co., Ltd., Tokyo 107-0062, Japan; [email protected] 9 Department of Veterinary Science, National Institute of Infectious Diseases, Tokyo 162-8640, Japan; [email protected] 10 Pacific Center for Emerging Infectious Diseases Research, John 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. -
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. -
Investigating the Role of Bats in Emerging Zoonoses
12 ISSN 1810-1119 FAO ANIMAL PRODUCTION AND HEALTH manual INVESTIGATING THE ROLE OF BATS IN EMERGING ZOONOSES Balancing ecology, conservation and public health interest Cover photographs: Left: © Jon Epstein. EcoHealth Alliance Center: © Jon Epstein. EcoHealth Alliance Right: © Samuel Castro. Bureau of Animal Industry Philippines 12 FAO ANIMAL PRODUCTION AND HEALTH manual INVESTIGATING THE ROLE OF BATS IN EMERGING ZOONOSES Balancing ecology, conservation and public health interest Edited by Scott H. Newman, Hume Field, Jon Epstein and Carol de Jong FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS Rome, 2011 Recommended Citation Food and Agriculture Organisation of the United Nations. 2011. Investigating the role of bats in emerging zoonoses: Balancing ecology, conservation and public health interests. Edited by S.H. Newman, H.E. Field, C.E. de Jong and J.H. Epstein. FAO Animal Production and Health Manual No. 12. Rome. The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO) concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specific companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO in preference to others of a similar nature that are not mentioned. The views expressed in this information product are those of the author(s) and do not necessarily reflect the views of FAO. -
The Mammals of Southern West Sepik Province, Papua New Guinea: Their Distribution, Abundance, Human Use and Zoogeography
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Flannery, Tim F., & Seri, L., 1990. The mammals of southern West Sepik Province, Papua New Guinea: their distribution, abundance, human use and zoogeography. Records of the Australian Museum 42(2): 173–208. [6 July 1990]. doi:10.3853/j.0067-1975.42.1990.114 ISSN 0067-1975 Published by the Australian Museum, Sydney naturenature cultureculture discover discover AustralianAustralian Museum Museum science science is is freely freely accessible accessible online online at at www.australianmuseum.net.au/publications/www.australianmuseum.net.au/publications/ 66 CollegeCollege Street,Street, SydneySydney NSWNSW 2010,2010, AustraliaAustralia Records of the Australian Museum (1990) Vol. 42: 173-208. ISSN 0067 1975 173 The Mammals of Southern West Sepik Province, Papua New Guinea: their Distribution, Abundance, Human Use and Zoogeography T.F. FLANNERyl & L. SERI2 IThe Australian Museum, 6 College Street, Sydney, NSW 2000, Australia 2Department of Environment and Conservation, Division of Wildlife, P.O. Box 6601, Boroko, Papua New Guinea ABSTRACT. A mammal survey was carried out between 1984 and 1987 in southern West Sepik Province, Papua New Guinea. Eleven major collecting localities, as well as some more minor ones, lying at altitudes of between 120 and 3,200 m were investigated. Voucher specimens for 87 indigenous mammal taxa were obtained, but research suggests that mammal diversity in the area may be as high as 120 species. This is the highest mammal diversity recorded anywhere in Australasia. A similar high bird diversity suggests that the area may be one of exceptionally high biodiversity overall. The most diverse mammal assemblages in the study area are found in the midmontane oak forests (between 1,500 and 2,500 m). -
AMERICAN MUSEUM NOVITATESI Published by Number 1140 the AMERICAN MUSEUM of NATURAL HISTORY August 20, 1941 New York City
AMERICAN MUSEUM NOVITATESI Published by Number 1140 THE AMERICAN MUSEUM OF NATURAL HISTORY August 20, 1941 New York City RESULTS OF THE ARCHBOLD EXPEDITIONS. No. 36 REMARKS ON SOME OLD WORLD LEAF-NOSED BATS BY G. H. H. TATE When reviewing recently the genus the cochleae (not so large, however, as in Hipposideros,I it became necessary to study H. muscinus). other available hipposiderine genera, to re- Many of the following notes are based examine Rhinolophus, and to some extent upon specimens kindly lent us by the Cu- to study the remaining leaf-nosed bats, the rators of Mammals at Washington, Chicago Megadermidae and Nyeteridae. and Cambridge. Material referable to Asellia, Anthops, Cloeotis, Triaenops, Coelops, Rhinolophus, Anthops ornatus Thomas Megaderma, Lavia, Nycteris, Lyroderma U.S.N.M. 123441, Guadalcanar. was examined. (Rhinonycteris is appar- Ears much as the "emarginate ears" of ently unrepresented in American collec- members of Hipposideros, but with anti- tions.) Notes made upon their compara- tragal fold somewhat larger. Horseshoe tive structures are presented herewith. with two lateral leaflets, the inner quite The hipposiderine genera are considered small, the outer large. Transverse leaf first, then briefly the Nyeteridae and with three raised, rounded processes, each Megadermidae. The isolated position of hollowed out behind and each representing Coelops is pointed out. Only incidental the extension of the three thickened septa remarks are offered on the Rhinolophinae, which in front support the leaf (as in H. reviewed two years ago2 and now in course larvatus). The transverse leaf subtended of extensive revision by C. C. Sanborn. by two small lateral leaflets of its own, A list of materials belonging to these separate from those margining the horse- genera contained in the Archbold collec- shoe. -
List of 28 Orders, 129 Families, 598 Genera and 1121 Species in Mammal Images Library 31 December 2013
What the American Society of Mammalogists has in the images library LIST OF 28 ORDERS, 129 FAMILIES, 598 GENERA AND 1121 SPECIES IN MAMMAL IMAGES LIBRARY 31 DECEMBER 2013 AFROSORICIDA (5 genera, 5 species) – golden moles and tenrecs CHRYSOCHLORIDAE - golden moles Chrysospalax villosus - Rough-haired Golden Mole TENRECIDAE - tenrecs 1. Echinops telfairi - Lesser Hedgehog Tenrec 2. Hemicentetes semispinosus – Lowland Streaked Tenrec 3. Microgale dobsoni - Dobson’s Shrew Tenrec 4. Tenrec ecaudatus – Tailless Tenrec ARTIODACTYLA (83 genera, 142 species) – paraxonic (mostly even-toed) ungulates ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BOVIDAE (46 genera) - cattle, sheep, goats, and antelopes 1. Addax nasomaculatus - Addax 2. Aepyceros melampus - Impala 3. Alcelaphus buselaphus - Hartebeest 4. Alcelaphus caama – Red Hartebeest 5. Ammotragus lervia - Barbary Sheep 6. Antidorcas marsupialis - Springbok 7. Antilope cervicapra – Blackbuck 8. Beatragus hunter – Hunter’s Hartebeest 9. Bison bison - American Bison 10. Bison bonasus - European Bison 11. Bos frontalis - Gaur 12. Bos javanicus - Banteng 13. Bos taurus -Auroch 14. Boselaphus tragocamelus - Nilgai 15. Bubalus bubalis - Water Buffalo 16. Bubalus depressicornis - Anoa 17. Bubalus quarlesi - Mountain Anoa 18. Budorcas taxicolor - Takin 19. Capra caucasica - Tur 20. Capra falconeri - Markhor 21. Capra hircus - Goat 22. Capra nubiana – Nubian Ibex 23. Capra pyrenaica – Spanish Ibex 24. Capricornis crispus – Japanese Serow 25. Cephalophus jentinki - Jentink's Duiker 26. Cephalophus natalensis – Red Duiker 1 What the American Society of Mammalogists has in the images library 27. Cephalophus niger – Black Duiker 28. Cephalophus rufilatus – Red-flanked Duiker 29. Cephalophus silvicultor - Yellow-backed Duiker 30. Cephalophus zebra - Zebra Duiker 31. Connochaetes gnou - Black Wildebeest 32. Connochaetes taurinus - Blue Wildebeest 33. Damaliscus korrigum – Topi 34.