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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 ..................................................................................................................... -
Bat Distribution Size Or Shape As Determinant of Viral Richness in African Bats
Bat Distribution Size or Shape as Determinant of Viral Richness in African Bats Gae¨l D. Maganga1,2., Mathieu Bourgarel1,3,4*., Peter Vallo5,6, Thierno D. Dallo7, Carine Ngoagouni8, Jan Felix Drexler7, Christian Drosten7, Emmanuel R. Nakoune´ 8, Eric M. Leroy1,9, Serge Morand3,10,11. 1 Centre International de Recherches Me´dicales de Franceville, Franceville, Gabon, 2 Institut National Supe´rieur d’Agronomie et de Biotechnologies (INSAB), Franceville, Gabon, 3 CIRAD, UPR AGIRs, Montpellier, France, 4 CIRAD, UPR AGIRs, Harare, Zimbabwe, 5 Institute of Vertebrate Biology, Academy of Sciences of the Czech Republic, Brno, Czech Republic, 6 Institute of Experimental Ecology, Ulm University, Ulm, Germany, 7 Institute of Virology, University of Bonn Medical Centre, Bonn, Germany, 8 Institut Pasteur de Bangui, Bangui, Re´publique Centrafricaine, 9 Institut de Recherche pour le De´veloppement, UMR 224 (MIVEGEC), IRD/CNRS/UM1, Montpellier, France, 10 Institut des Sciences de l’Evolution, CNRS-UM2, CC065, Universite´ de Montpellier 2, Montpellier, France, 11 Centre d’Infectiologie Christophe Me´rieux du Laos, Vientiane, Lao PDR Abstract The rising incidence of emerging infectious diseases (EID) is mostly linked to biodiversity loss, changes in habitat use and increasing habitat fragmentation. Bats are linked to a growing number of EID but few studies have explored the factors of viral richness in bats. These may have implications for role of bats as potential reservoirs. We investigated the determinants of viral richness in 15 species of African bats (8 Pteropodidae and 7 microchiroptera) in Central and West Africa for which we provide new information on virus infection and bat phylogeny. -
Mammals of Jordan
© Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Mammals of Jordan Z. AMR, M. ABU BAKER & L. RIFAI Abstract: A total of 78 species of mammals belonging to seven orders (Insectivora, Chiroptera, Carni- vora, Hyracoidea, Artiodactyla, Lagomorpha and Rodentia) have been recorded from Jordan. Bats and rodents represent the highest diversity of recorded species. Notes on systematics and ecology for the re- corded species were given. Key words: Mammals, Jordan, ecology, systematics, zoogeography, arid environment. Introduction In this account we list the surviving mammals of Jordan, including some reintro- The mammalian diversity of Jordan is duced species. remarkable considering its location at the meeting point of three different faunal ele- Table 1: Summary to the mammalian taxa occurring ments; the African, Oriental and Palaearc- in Jordan tic. This diversity is a combination of these Order No. of Families No. of Species elements in addition to the occurrence of Insectivora 2 5 few endemic forms. Jordan's location result- Chiroptera 8 24 ed in a huge faunal diversity compared to Carnivora 5 16 the surrounding countries. It shelters a huge Hyracoidea >1 1 assembly of mammals of different zoogeo- Artiodactyla 2 5 graphical affinities. Most remarkably, Jordan Lagomorpha 1 1 represents biogeographic boundaries for the Rodentia 7 26 extreme distribution limit of several African Total 26 78 (e.g. Procavia capensis and Rousettus aegypti- acus) and Palaearctic mammals (e. g. Eri- Order Insectivora naceus concolor, Sciurus anomalus, Apodemus Order Insectivora contains the most mystacinus, Lutra lutra and Meles meles). primitive placental mammals. A pointed snout and a small brain case characterises Our knowledge on the diversity and members of this order. -
Chiroptera: Pteropodidae)
Chapter 6 Phylogenetic Relationships of Harpyionycterine Megabats (Chiroptera: Pteropodidae) NORBERTO P. GIANNINI1,2, FRANCISCA CUNHA ALMEIDA1,3, AND NANCY B. SIMMONS1 ABSTRACT After almost 70 years of stability following publication of Andersen’s (1912) monograph on the group, the systematics of megachiropteran bats (Chiroptera: Pteropodidae) was thrown into flux with the advent of molecular phylogenetics in the 1980s—a state where it has remained ever since. One particularly problematic group has been the Austromalayan Harpyionycterinae, currently thought to include Dobsonia and Harpyionycteris, and probably also Aproteles.Inthis contribution we revisit the systematics of harpyionycterines. We examine historical hypotheses of relationships including the suggestion by O. Thomas (1896) that the rousettine Boneia bidens may be related to Harpyionycteris, and report the results of a series of phylogenetic analyses based on new as well as previously published sequence data from the genes RAG1, RAG2, vWF, c-mos, cytb, 12S, tVal, 16S,andND2. Despite a striking lack of morphological synapomorphies, results of our combined analyses indicate that Boneia groups with Aproteles, Dobsonia, and Harpyionycteris in a well-supported, expanded Harpyionycterinae. While monophyly of this group is well supported, topological changes within this clade across analyses of different data partitions indicate conflicting phylogenetic signals in the mitochondrial partition. The position of the harpyionycterine clade within the megachiropteran tree remains somewhat uncertain. Nevertheless, biogeographic patterns (vicariance-dispersal events) within Harpyionycterinae appear clear and can be directly linked to major biogeographic boundaries of the Austromalayan region. The new phylogeny of Harpionycterinae also provides a new framework for interpreting aspects of dental evolution in pteropodids (e.g., reduction in the incisor dentition) and allows prediction of roosting habits for Harpyionycteris, whose habits are unknown. -
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. -
2020 Special Issue
Journal Home page : www.jeb.co.in « E-mail : [email protected] Original Research Journal of Environmental Biology TM p-ISSN: 0254-8704 e-ISSN: 2394-0379 JEB CODEN: JEBIDP DOI : http://doi.org/10.22438/jeb/4(SI)/MS_1904 Plagiarism Detector Grammarly New records and present status of bat fauna in Mizoram, North-Eastern India C. Vanlalnghaka Department of Zoology, Govt. Serchhip College, Mizoram–796 181, India *Corresponding Author Email : [email protected] Paper received: 08.12.2019 Revised received: 24.06.2020 Accepted: 10.07.2020 Abstract Aim: The present study aimed to investigate the diversity of bat fauna in Mizoram and prepare a checklist for future references. This study also investigated threats and suggested recommendations for implementing conservation measures for bat fauna in Mizoram. Methodology: The present study was carried out in different parts of Mizoram between January 2012 - October 2019. Bats were trapped by using mist nets and hoop nets. Diagnostic morphological characters of bat were used for species identification. Digital camera and video camera were also used for further identification and documentation of bats. Results: During January 2012 – December 2016, eighteen bat species were identified. Recently, from January 2017 - October 2019 insectivorous bat species, Scotomanes ornatus was first time documented in Serchhip District (23.3 ºN 92.83 ºE), Mizoram. In total nineteen bat species were identified in this study, out of which ten species were first time recorded and nine species were rediscovered from the previous documentation. From the previous and present data, total of thirty-six bat Study the diversity of bat fauna and prepared checklist in species were recorded in Mizoram- nine Mizoram. -
Coral Mountain Resort Draft Eir Sch# 2021020310
CORAL MOUNTAIN RESORT DRAFT EIR SCH# 2021020310 TECHNICAL APPENDICES Focused Bat Survey Report Appendix D.2 June 2021 CARLSBAD FRESNO IRVINE LOS ANGELES PALM SPRINGS POINT RICHMOND May 6, 2021 RIVERSIDE ROSEVILLE Garret Simon SAN LUIS OBISPO CM Wave Development, LLC 2440 Junction Place, Suite 200 Boulder, Colorado 80301 Subject: Results of Focused Bat Surveys for the Proposed Wave at Coral Mountain Development Project in La Quinta, Riverside County, California Dear Mr. Simon: This letter documents the results of focused bat surveys performed by LSA Associates, Inc. (LSA) for the proposed Wave at Coral Mountain Project (project). The study area for the proposed project site comprises approximately 385 acres and is situated south of 58th Avenue and directly west of Madison Street in the City of La Quinta, in Riverside County, California. In order to determine whether the proposed project could result in potential adverse effects to bat species, a daytime bat-roosting habitat assessment was conducted to locate any suitable bat-roosting habitat within the study area. Follow-up nighttime acoustic and emergence surveys were performed in April 2021 at locations that were identified as having the potential to house roosting bats. In addition to discussing the results of the focused bat surveys, this document also provides recommendations to minimize potential project-related adverse effects to roosting bats. It should be noted that the focused nighttime survey results and the associated recommendations provided in this document are preliminary, and will be updated following the completion of additional nighttime acoustic and emergence surveys in June 2021. Performing the surveys in June, during the peak period of the maternity season when all local bat species can be expected to occupy their maternity roosts, will maximize the probability of detection for all bat species that may maternity roost within the study area. -
Anatomy and Histology of the Heart in Egyptian Fruit
Journal of Entomology and Zoology Studies 2016; 4(5): 50-56 E-ISSN: 2320-7078 P-ISSN: 2349-6800 JEZS 2016; 4(5): 50-56 Anatomy and histology of the heart in Egyptian © 2016 JEZS fruit bat (Rossetus aegyptiacus) Received: 09-09-2016 Accepted: 10-10-2016 Bahareh Alijani Bahareh Alijani and Farangis Ghassemi Department of Biology, Jahrom branch, Islamic Azad University, Abstract Jahrom, Iran This study was conducted to obtain more information about bats to help their conservation. Since 5 fruit Farangis Ghassemi bats, Rossetus aegyptiacus, weighing 123.04±0.08 g were captured using mist net. They were Department of Biology, Jahrom anesthetized and dissected in animal lab. The removed heart components were measured, fixed, and branch, Islamic Azad University, tissue processing was done. The prepared sections (5 µm) were subjected to Haematoxylin and Eosin Jahrom, Iran stain, and mounted by light microscope. Macroscopic and microscopic features of specimens were examined, and obtained data analyzed by ANOVA test. The results showed that heart was oval and closed in the transparent pericardium. The left and right side of heart were different significantly in volume and wall thickness of chambers. Heart was large and the heart ratio was 1.74%. Abundant fat cells, intercalated discs, and purkinje cells were observed. According to these results, heart in this species is similar to the other mammals and observed variation, duo to the high metabolism and energy requirements for flight. Keywords: Heart, muscle, bat, flight, histology 1. Introduction Bats are the only mammals that are able to fly [1]. Due to this feature, the variation in the [2, 3] morphology and physiology of their organs such as cardiovascular organs is expected Egyptian fruit bat (Rossetus aegyptiacus) belongs to order megachiroptera and it is the only megabat in Iran [4]. -
Bats (Chiroptera) from the Albertine Rift, Eastern Democratic Republic of Congo, with the Description of Two New Species of the Rhinolophus Maclaudi Group
Bonn zoological Bulletin 62 (2): 186 –202 December 2013 Bats (Chiroptera) from the Albertine Rift, eastern Democratic Republic of Congo, with the description of two new species of the Rhinolophus maclaudi group Julian C. Kerbis Peterhans 1,2 , Jakob Fahr 3, Michael H. Huhndorf 2, Prince Kaleme 4,5 , Andrew J. Plumptre 6, Ben D. Marks 2 & Robert Kizungu 5 1 College of Professional Studies, Roosevelt University, 430 S. Michigan Ave., Chicago, IL, 60605, USA 2 Science and Education, Field Museum of Natural History, Chicago, IL 60605-2496, USA, E-mail: [email protected] 3 Division of Evolutionary Biology, Zoological Institute, TU Braunschweig, Mendelssohnstr. 4, D-38106 Braunschweig, Germany 4 Department of Botany & Zoology, Stellenbosch University, Private Bag XI, Matieland, South Africa 5 Centre de Recherche des Sciences Naturelles, Lwiro, Democratic Republic of Congo 6 Wildlife Conservation Society , Plot 802 Kiwafu Rd, Kansanga, PO Box 7487, Kampala, Uganda Abstract . Horseshoe bats of the Rhinolophus maclaudi species group were recently revised by Fahr et al. (2002). Known members of the group are located in the mountainous region of West Africa and the Albertine Rift, east of the Congo River basin with a major gap (4300 km) between the two recognized sub-groups. Here we describe two additional species within this species group from the Albertine Rift center of endemism in the eastern Democratic Republic of Congo. One derives from the Misotschi-Kabogo highlands, a heretofore poorly documented region half-way down the western shore of Lake Tanganyika. Additional bat records from this locality are also documented. The second new taxon was collect - ed in Kahuzi-Biega National Park, a World Heritage Site adjacent to the shore of Lake Kivu. -
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.