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Cranial Morphology and Bite Force in Bats
CRANIOMANDIBULAR STRUCTURE AND FUNCTION IN MORMOOPID BATS A Thesis Presented to the faculty of the Department of Biological Sciences California State University, Sacramento Submitted in partial satisfaction of the requirements for the degree of MASTER OF SCIENCE in Biological Sciences by Jeffrey B. Changaris FALL 2017 © 2017 Jeffrey B. Changaris ALL RIGHTS RESERVED ii CRANIOMANDIBULAR STRUCTURE AND FUNCTION IN MORMOOPID BATS A Thesis by Jeffrey B. Changaris Approved by: ____________________________________, Committee Chair Dr. Ronald M. Coleman ____________________________________, Second Reader Dr. Winston C. Lancaster ____________________________________, Third Reader Dr. Joseph Bahlman ___________________________ Date iii Student: Jeffrey B. Changaris I certify that this student has met the requirements for format contained in the University format manual, and that this thesis is suitable for shelving in the Library and credit is to be awarded for the thesis. ____________________________, Graduate Coordinator _________________ Dr. James W. Baxter Date Department of Biological Sciences iv Abstract of CRANIOMANDIBULAR STRUCTURE AND FUNCTION IN MORMOOPID BATS by Jeffrey B. Changaris Neotropical Ghost-Faced bats of the genus Mormoops (Order Chiroptera, Family Mormoopidae) have a radically upturned rostrum, or snout, while the other mormoopid genus, Pteronotus, has only a slight upturning of the rostrum. This type of difference in morphology between closely related taxa is likely to be the result of some sort of specialization. Observation of Mormoops blainvillei, the Antillean Ghost-Faced bat, reveals that they can open their mouths very wide relative to the size of their heads. Mormoopid bats are insectivorous with Mormoops blainvillei having a prey preference of large moths, but related species, such as Pteronotus quadridens, the Sooty Mustached bat, have a more varied diet with a large component of smaller hard-bodied beetles. -
Conservation Ecology of Cave Bats
Chapter 15 Conservation Ecology of Cave Bats Neil M. Furey and Paul A. Racey Abstract Caves and other subterranean sites such as mines are critical to the sur- vival of hundreds of bat species worldwide, since they often provide shelter for most of a nation’s bat fauna. In the temperate zone, caves provide roosts for hiber- nation and for some species, breeding in summer, whereas in warmer regions, they support high species richness year round and enormous colonies that maintain substantial ecosystem services. Due to the solubility of the substrate, the highest densities of caves occur in karst landscapes. Given their importance for bats, rel- atively few studies have investigated factors involved in cave selection, although current evidence suggests that the density and size of caves are the best predictors of species diversity and population sizes. Thermal preferences have been estab- lished for some cave-dwelling species as well as their vulnerability to disturbance, particularly during hibernation and reproduction. Growth in limestone quarrying and cave tourism industries worldwide severely threatens cave-dwelling bats, in addition to loss of foraging habitat, hunting for bushmeat, incidental disturbance and disruptive guano harvesting. Apparent declines of cave bats in Europe and North America also pose serious concerns, as do global climate change predic- tions. The main conservation response to threats to cave bats in these continents N.M. Furey (*) Fauna & Flora International (Cambodia Programme), No. 19, Street 360, Boeng Keng Kang 1, PO Box 1380, Phnom Penh 12000, Cambodia e-mail: [email protected] P.A. Racey Centre for Ecology and Conservation, College of Life and Environmental Sciences, University of Exeter, Cornwall Campus, Treliever Road, Penryn TR10 9EZ, UK e-mail: [email protected] © The Author(s) 2016 463 C.C. -
Diversity of Bat Species Across Dominica
Diversity of Bat Species across Dominica Brittany Moore, Hannah Rice, Meredith Stroud Texas A&M University Tropical Field Biology Dominica 2015 Dr. Thomas Lacher Dr. Jim Woolley Abstract: Twelve species of bats can be found on the island of Dominica, however there are still some species that have not been thoroughly catalogued. Our report is based on further findings regarding Artibeus jamaicensis, Sturnira lilium, Ardops nichollsi, Myotis dominicensis, Monophyllus plethodon and Brachyphylla cavernarum. We collected mass, forearm length, hind foot length, ear length, sex, and reproductive condition for every individual bat and then compared this information among species to observe morphological differences. We also added new data to past studies on wing loading and aspect ratios for the species we caught. We found a statistical significance among species in body size measure and wing morphology. Among the bats examined, the measurements can be used in order to positively identify species. Introduction: Dominica, also known as the Nature Island, is home to a great diversity of plants and animals. There are many various habitats ranging from dry forest to montane and elfin rainforest. Within each habitat, one may find species only endemic to that area. Animal activity at night in Dominica is quite different than what can be witnessed during the day. As nighttime falls, the call of the tink frog can be heard all over the island, and the mating click beetles will illuminate even the darkest of forests, but by far the most exciting nocturnal animals are the thousands of bats that come alive when the sun begins to set. -
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. -
Puerto Rico Comprehensive Wildlife Conservation Strategy 2005
Comprehensive Wildlife Conservation Strategy Puerto Rico PUERTO RICO COMPREHENSIVE WILDLIFE CONSERVATION STRATEGY 2005 Miguel A. García José A. Cruz-Burgos Eduardo Ventosa-Febles Ricardo López-Ortiz ii Comprehensive Wildlife Conservation Strategy Puerto Rico ACKNOWLEDGMENTS Financial support for the completion of this initiative was provided to the Puerto Rico Department of Natural and Environmental Resources (DNER) by U.S. Fish and Wildlife Service (USFWS) Federal Assistance Office. Special thanks to Mr. Michael L. Piccirilli, Ms. Nicole Jiménez-Cooper, Ms. Emily Jo Williams, and Ms. Christine Willis from the USFWS, Region 4, for their support through the preparation of this document. Thanks to the colleagues that participated in the Comprehensive Wildlife Conservation Strategy (CWCS) Steering Committee: Mr. Ramón F. Martínez, Mr. José Berríos, Mrs. Aida Rosario, Mr. José Chabert, and Dr. Craig Lilyestrom for their collaboration in different aspects of this strategy. Other colleagues from DNER also contributed significantly to complete this document within the limited time schedule: Ms. María Camacho, Mr. Ramón L. Rivera, Ms. Griselle Rodríguez Ferrer, Mr. Alberto Puente, Mr. José Sustache, Ms. María M. Santiago, Mrs. María de Lourdes Olmeda, Mr. Gustavo Olivieri, Mrs. Vanessa Gautier, Ms. Hana Y. López-Torres, Mrs. Carmen Cardona, and Mr. Iván Llerandi-Román. Also, special thanks to Mr. Juan Luis Martínez from the University of Puerto Rico, for designing the cover of this document. A number of collaborators participated in earlier revisions of this CWCS: Mr. Fernando Nuñez-García, Mr. José Berríos, Dr. Craig Lilyestrom, Mr. Miguel Figuerola and Mr. Leopoldo Miranda. A special recognition goes to the authors and collaborators of the supporting documents, particularly, Regulation No. -
Environmental Impact Assessment
Environmental Impact Assessment CAEL Wind Farm, Great Valley Manchester September 2012 EIA for a Wind Farm at Great Valley Manchester by CAEL September 2012 Table of Contents 1.0 Introduction ........................................................................................................................................... 6 1.1 Background and Project Rationale ................................................................................................. 6 2.0 Project Description ............................................................................................................................. 11 2.1 Project Location .............................................................................................................................. 11 2.2 Project Design ................................................................................................................................. 14 2.3 Transportation and Road Widening ............................................................................................. 25 2.4 Access Road Design ....................................................................................................................... 29 Figure 12: Layout of Access Routes to Turbines ................................................................................... 30 2.5 Project Schedule and Project Management Team ...................................................................... 31 2.6 Decommissioning........................................................................................................................... -
Neotropical Nectar-Feeding Bats (Family Phyllostomidae) Revisited: Lingual Data Support a Recently-Proposed Molecular Phylogeny
Illinois Wesleyan University Digital Commons @ IWU Honors Projects Biology 4-25-2001 Neotropical Nectar-feeding Bats (Family Phyllostomidae) Revisited: Lingual Data Support a Recently-Proposed Molecular Phylogeny Shawn De La Mar '01 Illinois Wesleyan University Follow this and additional works at: https://digitalcommons.iwu.edu/bio_honproj Part of the Biology Commons Recommended Citation De La Mar '01, Shawn, "Neotropical Nectar-feeding Bats (Family Phyllostomidae) Revisited: Lingual Data Support a Recently-Proposed Molecular Phylogeny" (2001). Honors Projects. 5. https://digitalcommons.iwu.edu/bio_honproj/5 This Article is protected by copyright and/or related rights. It has been brought to you by Digital Commons @ IWU with permission from the rights-holder(s). You are free to use this material in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s) directly, unless additional rights are indicated by a Creative Commons license in the record and/ or on the work itself. This material has been accepted for inclusion by faculty at Illinois Wesleyan University. For more information, please contact [email protected]. ©Copyright is owned by the author of this document. Neotropical Nectar-feeding Bats (Family PhyUostomidae) Revisited: Lingual Data Support a Recently-proposed Molecular Phylogeny. A Senior Research Honors Paper Presented By Shawn De La Mar Deparbnent ofBiology Illinois Wesleyan University April 25, 2001 Neotropical Nectar-feeding Bats Revisited: Lingual Data Support a Recently proposed Molecular Phylogeny. A Senior Research Honors Paper Presented by Shawn De La Mar Department of Biology Illinois Wesleyan University April 25, 2001 Approved as to style and content by: Th~~Ri:t~F=gy;':;'=IL..WU----- Research Advisor Charles Springwood, pt. -
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. -
Echolocation Calls and Wing Morphology of Bats from the West Indies
Acta Chiropterologica, 6(1): 75–90, 2004 PL ISSN 1508–1109 © Museum and Institute of Zoology PAS Echolocation calls and wing morphology of bats from the West Indies NANCY VAUGHAN JENNINGS1, STUART PARSONS2, KATE E. BARLOW3, and MICHAEL R. GANNON4 1School of Biological Sciences, University of Bristol, Woodland Road, Bristol BS8 1UG, United Kingdom E-mail: [email protected] 2School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand 32 The Paddock, Seton Mains, Longniddry, East Lothian, EH32 0PG, United Kingdom Previous address: School of Biological Sciences, University of Bristol, Woodland Road, Bristol BS8 1UG, United Kingdom 4Department of Biology, The Pennsylvania State University, Altoona College, 3000 Ivyside Park Altoona, PA 16601-3760, USA Echolocation calls of 119 bats belonging to 12 species in three families from Antillean islands of Puerto Rico, Dominica, and St. Vincent were recorded by using time-expansion methods. Spectrograms of calls and descriptive statistics of five temporal and frequency variables measured from calls are presented. The echolocation calls of many of these species, particularly those in the family Phyllostomidae, have not been described previously. The wing morphology of each taxon is described and related to the structure of its echolocation calls and its foraging ecology. Of slow aerial-hawking insectivores, the Mormoopidae and Natalidae Mormoops blainvillii, Pteronotus davyi davyi, P. quadridens fuliginosus, and Natalus stramineus stramineus can forage with great manoeuvrability in background-cluttered space (close to vegetation), and are able to hover. Pteronotus parnellii portoricensis is able to fly and echolocate in highly-cluttered space (dense vegetation). Among frugivores, nectarivores and omnivores in the family Phyllostomidae, Brachyphylla cavernarum intermedia is adapted to foraging in the edges of vegetation in background-cluttered space, while Erophylla bombifrons bombifrons, Glossophaga longirostris rostrata, Artibeus jamaicensis jamaicensis, A. -
1 a Photographic Field Guide to the Bats of the West Indian Island Of
A Photographic Field Guide to the Bats of the West Indian Island of Dominica Lloyd W. Towers III Dominica 2007 Dr. James Woolley Dr. Robert Wharton Texas A&M University 1 ABSTRACT No current field guide incorporates photographs and descriptions of all of the species of bats known to occur on the island of Dominica. The guide presented here is based on bats captured using mist nets and insect nets at various locations on the Archbold Tropical Research and Education Center and the Morne Trois Pitons National Park in Dominica. The field guide provides several pictures that show important identifying features of the five bat species that were captured. INTRODUCTION There are 12 species of bats found on Dominica. These are as follows: Pteronotus davyi, Noctilio leporinus, Brachyphylla cavernarum, Monophyllus plethodon, Artibeus jamaicensis, Ardops nichollsi, Sturnira lilium, Natalus stramineus, Eptesicus fuscus, Myotis dominicensis, Tadarida brasiliensis, and Molossus molossus (Genoways et al. 2001). Several field guides have been created for Antillean bats, but there is not a field guide with photographs specifically for the bats of Dominica. Gannon et al. (2005) provided an illustrated field guide entitled Bats of Puerto Rico, and it provided illustrations and descriptions of N. leporinus, A. jamaicensis, B. cavernarum, E. fuscus, T. brasiliensis, and M. molossus. However, there were not many photographs of the bats and the field guide was only concerned with Puerto Rico. Baker et al. (1984) provided an identification key with photographs of N. leporinus, B. cavernarum, A. jamaicensis, A. nichollsi, S. lilium, M. dominicensis, T. brasiliensis, and M. molossus in their publication Occasional Papers: Field Guide to Antillean Bats, but again, the focus of the publication was not on Dominica specifically. -
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. -
Caribbean Naturalist No
Caribbean Naturalist No. 35 2016 Conservation Value of Remnant Habitat for Neotropical Bats on Islands Armando Rodríguez-Durán and Waldemar Feliciano-Robles The Caribbean Naturalist . ♦ A peer-reviewed and edited interdisciplinary natural history science journal with a re- gional focus on the Caribbean ( ISSN 2326-7119 [online]). ♦ Featuring research articles, notes, and research summaries on terrestrial, fresh-water, and marine organisms, and their habitats. The journal's versatility also extends to pub- lishing symposium proceedings or other collections of related papers as special issues. ♦ Focusing on field ecology, biology, behavior, biogeography, taxonomy, evolution, anatomy, physiology, geology, and related fields. Manuscripts on genetics, molecular biology, anthropology, etc., are welcome, especially if they provide natural history in- sights that are of interest to field scientists. ♦ Offers authors the option of publishing large maps, data tables, audio and video clips, and even powerpoint presentations as online supplemental files. ♦ Proposals for Special Issues are welcome. ♦ Arrangements for indexing through a wide range of services, including Web of Knowledge (includes Web of Science, Current Contents Connect, Biological Ab- stracts, BIOSIS Citation Index, BIOSIS Previews, CAB Abstracts), PROQUEST, SCOPUS, BIOBASE, EMBiology, Current Awareness in Biological Sciences (CABS), EBSCOHost, VINITI (All-Russian Institute of Scientific and Technical Information), FFAB (Fish, Fisheries, and Aquatic Biodiversity Worldwide), WOW (Waters and Oceans Worldwide), and Zoological Record, are being pursued. ♦ The journal staff is pleased to discuss ideas for manuscripts and to assist during all stages of manuscript preparation. The journal has a mandatory page charge to help defray a portion of the costs of publishing the manuscript. Instructions for Authors are available online on the journal’s website (www.eaglehill.us/cana).