The Part of Bat Research
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Floral Biology and Pollination Strategy of Durio (Malvaceae) in Sarawak, Malaysian Borneo
BIODIVERSITAS ISSN: 1412-033X Volume 21, Number 12, December 2020 E-ISSN: 2085-4722 Pages: 5579-5594 DOI: 10.13057/biodiv/d211203 Floral biology and pollination strategy of Durio (Malvaceae) in Sarawak, Malaysian Borneo NG WIN SENG1, JAYASILAN MOHD-AZLAN1, WONG SIN YENG1,2,♥ 1Institute of Biodiversity and Environmental Conservation, Universiti Malaysia Sarawak. 94300 Kota Samarahan, Sarawak, Malaysia. 2Harvard University Herbaria. 22 Divinity Avenue, Cambridge, MA 02138, United States of America. ♥ email: [email protected]. Manuscript received: 25 September 2020. Revision accepted: 4 November 2020. Abstract. Ng WS, Mohd-Azlan J, Wong SY. 2020. Floral biology and pollination strategy of Durio (Malvaceae) in Sarawak, Malaysian Borneo. Biodiversitas 21: 5579-5594. This study was carried out to investigate on the flowering mechanisms of four Durio species in Sarawak. The anthesis started in the afternoon (D. graveolens and D. zibethinus), evening (D. kutejensis) or midnight (D. griffithii); and lasted between 11.5 hours (D. griffithii) to 20 hours (D. graveolens). All four Durio species are generalists. Individuals of a fruit bat (Eonycteris spelaea, Pteropodidae) are considered as the main pollinator for D. graveolens, D. kutejensis, and D. zibethinus while spiderhunter (Arachnothera, Nectariniidae) is also proposed as a primary pollinator for D. kutejensis. Five invertebrate taxa were observed as secondary or inadvertent pollinators of Durio spp.: honeybee, Apis sp. (Apidae), stingless bee, Tetrigona sp. (Apidae), nocturnal wasp, Provespa sp. (Vespidae), pollen beetle (Nitidulidae), and thrip (Thysanoptera). Honey bees and stingless bees pollinated all four Durio species. Pollen beetles were found to pollinate D. griffithii and D. graveolens while nocturnal wasps were found to pollinate D. -
2021 Fur Harvester Digest 3 SEASON DATES and BAG LIMITS
2021 Michigan Fur Harvester Digest RAP (Report All Poaching): Call or Text (800) 292-7800 Michigan.gov/Trapping Table of Contents Furbearer Management ...................................................................3 Season Dates and Bag Limits ..........................................................4 License Types and Fees ....................................................................6 License Types and Fees by Age .......................................................6 Purchasing a License .......................................................................6 Apprentice & Youth Hunting .............................................................9 Fur Harvester License .....................................................................10 Kill Tags, Registration, and Incidental Catch .................................11 When and Where to Hunt/Trap ...................................................... 14 Hunting Hours and Zone Boundaries .............................................14 Hunting and Trapping on Public Land ............................................18 Safety Zones, Right-of-Ways, Waterways .......................................20 Hunting and Trapping on Private Land ...........................................20 Equipment and Fur Harvester Rules ............................................. 21 Use of Bait When Hunting and Trapping ........................................21 Hunting with Dogs ...........................................................................21 Equipment Regulations ...................................................................22 -
Diversity and Evolution of Viral Pathogen Community in Cave Nectar Bats (Eonycteris Spelaea)
viruses Article Diversity and Evolution of Viral Pathogen Community in Cave Nectar Bats (Eonycteris spelaea) Ian H Mendenhall 1,* , Dolyce Low Hong Wen 1,2, Jayanthi Jayakumar 1, Vithiagaran Gunalan 3, Linfa Wang 1 , Sebastian Mauer-Stroh 3,4 , Yvonne C.F. Su 1 and Gavin J.D. Smith 1,5,6 1 Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore 169857, Singapore; [email protected] (D.L.H.W.); [email protected] (J.J.); [email protected] (L.W.); [email protected] (Y.C.F.S.) [email protected] (G.J.D.S.) 2 NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore 119077, Singapore 3 Bioinformatics Institute, Agency for Science, Technology and Research, Singapore 138671, Singapore; [email protected] (V.G.); [email protected] (S.M.-S.) 4 Department of Biological Sciences, National University of Singapore, Singapore 117558, Singapore 5 SingHealth Duke-NUS Global Health Institute, SingHealth Duke-NUS Academic Medical Centre, Singapore 168753, Singapore 6 Duke Global Health Institute, Duke University, Durham, NC 27710, USA * Correspondence: [email protected] Received: 30 January 2019; Accepted: 7 March 2019; Published: 12 March 2019 Abstract: Bats are unique mammals, exhibit distinctive life history traits and have unique immunological approaches to suppression of viral diseases upon infection. High-throughput next-generation sequencing has been used in characterizing the virome of different bat species. The cave nectar bat, Eonycteris spelaea, has a broad geographical range across Southeast Asia, India and southern China, however, little is known about their involvement in virus transmission. -
Karwar, Close to the National Highway 17 (NH-17)
E421 VOL. 9 Wilsol In association with Public Disclosure Authorized IJiE IIIE Phase II - Environment Assessment Report for the Segment of Corridor 13A which passes through Dandeli Wildlife and Anshi National Park Public Disclosure Authorized Project Co-ordinating Consultancy Services (PCC) For the Karnataka State Highways Improvement Project IBRD Loan/Credit No. LN-4114 Belga Wi~~~~~dar Public Disclosure Authorized Karwa.r Mangalor, -g)alore Public Disclosure Authorized Prepared for Gov, of Karnataka Pubi c Works Dept. (PIU,KSHIP) Jqnuary 2005 EXECUTIVE SUMMARY Karnataka State Highways Environnmental Assessment Reportfor the Segmenit of Improvement Project Corridorl3A which passes tlroughi Dandeli Wildlife Sanctuary and Anshi National Park EXECUTIVE SUMMARY 1. Introduction Corridor 13A, also known as State Highway 95 (SH 95), commences at Ramanagar junction on NH-4A near Londa in Belgaum District, enters Uttarakannada District and ends at Sadashivgadh, near Karwar, close to the National Highway 17 (NH-17). The total length of this Corridor is 121 Km and it offers c onnectivity to Belgaum, Karwar and Goa. This corridor passes through the Dandeli Wildlife Sanctuary and Anshi National Park. Corridor 13A has been selected for rehabilitation under the Kamataka State Highways Improvement Project (KSHIP). 2. Project Road A 28 km section of Corridor 13A i.e from chainage 55.57 Km to 83.41 Km, passes through the Dandeli Wildlife Sanctuary and the Anshi National Park. The corridor traverses buffer and core zones w ith undulating and hilly terrain t hroughout its e ntire length. T he width o f t he e xisting carriageway varies from 3.75m to 5.5m. -
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. -
Fur, Skin, and Ear Mites (Acariasis)
technical sheet Fur, Skin, and Ear Mites (Acariasis) Classification flank. Animals with mite infestations have varying clinical External parasites signs ranging from none to mild alopecia to severe pruritus and ulcerative dermatitis. Signs tend to worsen Family as the animals age, but individual animals or strains may be more or less sensitive to clinical signs related Arachnida to infestation. Mite infestations are often asymptomatic, but may be pruritic, and animals may damage their skin Affected species by scratching. Damaged skin may become secondarily There are many species of mites that may affect the infected, leading to or worsening ulcerative dermatitis. species listed below. The list below illustrates the most Nude or hairless animals are not susceptible to fur mite commonly found mites, although other mites may be infestations. found. Humans are not subject to more than transient • Mice: Myocoptes musculinus, Myobia musculi, infestations with any of the above organisms, except Radfordia affinis for O. bacoti. Transient infestations by rodent mites may • Rats: Ornithonyssus bacoti*, Radfordia ensifera cause the formation of itchy, red, raised skin nodules. Since O. bacoti is indiscriminate in its feeding, it will • Guinea pigs: Chirodiscoides caviae, Trixacarus caviae* infest humans and may carry several blood-borne • Hamsters: Demodex aurati, Demodex criceti diseases from infected rats. Animals with O. bacoti • Gerbils: (very rare) infestations should be treated with caution. • Rabbits: Cheyletiella parasitivorax*, Psoroptes cuniculi Diagnosis * Zoonotic agents Fur mites are visible on the fur using stereomicroscopy and are commonly diagnosed by direct examination of Frequency the pelt or, with much less sensitivity, by examination Rare in laboratory guinea pigs and gerbils. -
A Checklist of the Mammals of South-East Asia
A Checklist of the Mammals of South-east Asia A Checklist of the Mammals of South-east Asia PHOLIDOTA Pangolin (Manidae) 1 Sunda Pangolin (Manis javanica) 2 Chinese Pangolin (Manis pentadactyla) INSECTIVORA Gymnures (Erinaceidae) 3 Moonrat (Echinosorex gymnurus) 4 Short-tailed Gymnure (Hylomys suillus) 5 Chinese Gymnure (Hylomys sinensis) 6 Large-eared Gymnure (Hylomys megalotis) Moles (Talpidae) 7 Slender Shrew-mole (Uropsilus gracilis) 8 Kloss's Mole (Euroscaptor klossi) 9 Large Chinese Mole (Euroscaptor grandis) 10 Long-nosed Chinese Mole (Euroscaptor longirostris) 11 Small-toothed Mole (Euroscaptor parvidens) 12 Blyth's Mole (Parascaptor leucura) 13 Long-tailed Mole (Scaptonyx fuscicauda) Shrews (Soricidae) 14 Lesser Stripe-backed Shrew (Sorex bedfordiae) 15 Myanmar Short-tailed Shrew (Blarinella wardi) 16 Indochinese Short-tailed Shrew (Blarinella griselda) 17 Hodgson's Brown-toothed Shrew (Episoriculus caudatus) 18 Bailey's Brown-toothed Shrew (Episoriculus baileyi) 19 Long-taied Brown-toothed Shrew (Episoriculus macrurus) 20 Lowe's Brown-toothed Shrew (Chodsigoa parca) 21 Van Sung's Shrew (Chodsigoa caovansunga) 22 Mole Shrew (Anourosorex squamipes) 23 Himalayan Water Shrew (Chimarrogale himalayica) 24 Styan's Water Shrew (Chimarrogale styani) Page 1 of 17 Database: Gehan de Silva Wijeyeratne, www.jetwingeco.com A Checklist of the Mammals of South-east Asia 25 Malayan Water Shrew (Chimarrogale hantu) 26 Web-footed Water Shrew (Nectogale elegans) 27 House Shrew (Suncus murinus) 28 Pygmy White-toothed Shrew (Suncus etruscus) 29 South-east -
Texas Wildlife Identification Guide: a Guide to Game Animals, Game
texas parks and wildlife TEXAS WILDLIFE IDENTIFICATION GUIDE A guide to game animals, game birds, furbearers and other wildlife of Texas. INTRODUCTION TEXAS game animals, game birds, furbearers and other wildlife are important for many reasons. They provide countless hours of viewing and recreational opportunities.They benefit the Texas economy through hunting and “nature tourism” such as birdwatching. Commercial businesses that provide birdseed, dry corn and native landscaping may be devoted solely to attracting many of the animals found in this book. Local hunting and trapping economies, guiding operations and hunting leases have prospered because of the abun- dance of these animals in Texas.The Texas Parks and Wildlife Department benefits because of hunting license sales, but it uses these funds to research, manage and pro- tect all wildlife populations – not just game animals. Game animals provide humans with cultural, social, aesthetic and spiritual pleasures found in wildlife art, taxi- dermy and historical artifacts. Conservation organizations dedicated to individual species such as quail, turkey and deer, have funded thousands of wildlife projects throughout North America, demonstrating the mystique game animals have on people. Animals referenced in this pocket guide exist because their habitat exists in Texas. Habitat is food, cover, water and space, all suitably arranged.They are part of a vast food chain or web that includes thousands more species of wildlife such as the insects, non-game animals, fish and i rare/endangered species. Active management of wild landscapes is the primary means to continue having abundant populations of wildlife in Texas. Preservation of rare and endangered habitat is one way of saving some species of wildlife such as the migratory whooping crane that makes Texas its home in the winter. -
Brachyphylla Nana
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Mammalogy Papers: University of Nebraska State Museum Museum, University of Nebraska State December 1983 Brachyphylla nana Pierre Swanepoel Kaffrarian Museum, King William’s Town, 5600, Republic of South Africa Hugh H. Genoways University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/museummammalogy Part of the Zoology Commons Swanepoel, Pierre and Genoways, Hugh H., "Brachyphylla nana" (1983). Mammalogy Papers: University of Nebraska State Museum. 94. https://digitalcommons.unl.edu/museummammalogy/94 This Article is brought to you for free and open access by the Museum, University of Nebraska State at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Mammalogy Papers: University of Nebraska State Museum by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Brachyphylla nana. BY Pierre swanepoel and ugh H. Genoways Published 15 December 1983 by The American Society of Mammalogists Brachyphylla nana Miller, 1902 1977); Cueva de Paredones, Habana Province (Woloszyn and Silva- Taboada, 1977); Cuba (Arredondo, 1970; Mayo, 1970); St. Michel, Greater Antillean Fruit-eating Bat Haiti (Miller, 1929); Isle of Pines (Peterson, 1917); Dairy Cave, Brachyphylla nana Miller, 1902:409. Type locality El Guami, St. .4nn Parish, Jamaica (Koopman and Williams, 1951); Portland Pinar de Rio, Cuba. Cave, Clarendon Parish, Jamaica (Williams, 1952). Brachyphylla purnlla Miller. 1918:39. Type locality Port-de-Paix, Swanepoel and Genoways (1978) re-examined the material Haiti. collected at Dairy Cave, St. Ann Parish, Jamaica. This Pleistocene or sub-Recent fossil material generally averaged larger than Recent CONTEXT AND CONTENT. -
A Phylogeny of the Neotropical Nectar-Feeding Bats (Chiroptera: Phyllostomidae) Based on Morphological and Molecular Data
Journal of Mammalian Evolution, Vol. 9, No. 1/ 2, June 2002 ( 2002) A Phylogeny of the Neotropical Nectar-Feeding Bats (Chiroptera: Phyllostomidae) Based on Morphological and Molecular Data Bryan C. Carstens,1,3 Barbara L. Lundrigan,1 and Philip Myers,2 We present a phylogeny of 35 species of nectar-feeding bats based on 119 morphological characters: 62 from the skin, skull, and dentition and 57 soft tissue characters (the latter from Wetterer et al., 2000). These data support monophyly of the subfamilies Brachyphyllinae, Phyllonycterinae, and Glossophaginae, and the tribes Glossophagini and Lonchophyllini. Our analysis contradicts the phylogeny estimated from the RAG-2 gene, which does not support a monophyletic Glossophaginae (Baker et al., 2000). Parsimony analysis of a combined matrix, containing morphological characters and RAG-2 sequences, results in a phylogeny that includes Brachyphyllinae and Phyllonycterinae in Glossophaginae. Support for most clades is stronger than in the morphological tree, but support for basal nodes of the phylogeny remains weak. The weak support at these basal nodes underscores the historical disagreements regarding relationships among these taxa; combining morphological and molecular data has not improved support for these nodes. Uncertainty regarding basal relationships complicates description of morphological change during the evolution of nectarivory in the Phyllostomidae. KEY WORDS: Phyllostomidae, Glossophaginae, Brachyphyllinae, Phyllonycterinae, nectar-feeding, RAG-2. INTRODUCTION The taxonomic history of the nectar-feeding phyllostomid bats has been dominated by questions pertaining to the relationships among three major groups (Table I), the Caribbean subfamilies Brachyphyllinae and Phyllonycterinae and the more broadly dis- tributed Glossophaginae. There has been little consensus regarding relationships among these groups. -
University of Florida Thesis Or Dissertation Formatting
ECOSYSTEM SERVICES OF PTEROPODID BATS, WITH SPECIAL ATTENTION TO FLYING FOXES (PTEROPUS AND ACERODON) IN SULAWESI, INDONESIA By SHEHERAZADE A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2018 © 2018 Sheherazade To my mom Thank you for teaching me how to be an independent, strong, and happy woman ACKNOWLEDGMENTS I would like to thank my advisor, Dr. Holly Ober, for her guidance and patience during my study. I thank her for always encouraging me to maximize all learning opportunities to gain skills and knowledge that will be important for my future. I thank Dr. Bette Loiselle and Dr. Todd Palmer for their invaluable advice to this study and thesis. I thank the Center for International Forestry and United States Agency for International Development for funding my master program. I thank Dr. Steven Lawry, Ms. Dina Hubuddin, Ms. Rahayu Koesnadi, Ms. Raya Soendjoto, Dr. Karen Kainer, and Dr. Bette Loiselle for providing supports and managing administrative issues during my entire study. I thank Tropical Conservation and Development (TCD) University of Florida for allowing me to learn about the interdisciplinary aspects of conservation and awarding me a field research grant. I thank Rufford Small Grant, Bat Conservation International, and IdeaWild for also funding my research. I thank Government Agency of Maritime Affairs and Fisheries of Central Sulawesi, Integrated Permit Service Agency of Central and West Sulawesi, Longkoga Barat/Timur village, Bualemo Subdistrict, Batetangnga village and Binuang Subdistrict for permits. I thank Alliance for Tompotika Conservation and my team for their tremendous assistance in the field. -
Understanding Phylogenetic Incongruence: Lessons from Phyllostomid Bats
Biol. Rev. (2012), 87, pp. 991–1024. 991 doi: 10.1111/j.1469-185X.2012.00240.x Understanding phylogenetic incongruence: lessons from phyllostomid bats Liliana M. Davalos´ 1,∗, Andrea L. Cirranello2,3,∗, Jonathan H. Geisler4 and Nancy B. Simmons2 1 Department of Ecology and Evolution, and Consortium for Inter-Disciplinary Environmental Research, State University of New York at Stony Brook, Stony Brook, NY 11794, USA 2 Division of Vertebrate Zoology (Mammalogy), American Museum of Natural History, New York, NY 10024, USA 3 Department of Anatomical Sciences, State University of New York at Stony Brook, Stony Brook, NY 11794, USA 4 Department of Anatomy, New York College of Osteopathic Medicine, Old Westbury, NY 11568, USA ABSTRACT All characters and trait systems in an organism share a common evolutionary history that can be estimated using phylogenetic methods. However, differential rates of change and the evolutionary mechanisms driving those rates result in pervasive phylogenetic conflict. These drivers need to be uncovered because mismatches between evolutionary processes and phylogenetic models can lead to high confidence in incorrect hypotheses. Incongruence between phylogenies derived from morphological versus molecular analyses, and between trees based on different subsets of molecular sequences has become pervasive as datasets have expanded rapidly in both characters and species. For more than a decade, evolutionary relationships among members of the New World bat family Phyllostomidae inferred from morphological and molecular data have been in conflict. Here, we develop and apply methods to minimize systematic biases, uncover the biological mechanisms underlying phylogenetic conflict, and outline data requirements for future phylogenomic and morphological data collection.