Sleeping in the Leaves
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Conflicting Evolutionary Histories of the Mitochondrial and Nuclear
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Commons @ ACU Abilene Christian University Digital Commons @ ACU Biology College of Arts and Sciences 8-26-2017 Conflicting vE olutionary Histories of the Mitochondrial and Nuclear Genomes in New World Myotis Bats Thomas Lee Jr. Abilene Christian University, [email protected] Follow this and additional works at: https://digitalcommons.acu.edu/biology Part of the Biology Commons Recommended Citation Lee, Thomas Jr., "Conflicting vE olutionary Histories of the Mitochondrial and Nuclear Genomes in New World Myotis Bats" (2017). Biology. 2. https://digitalcommons.acu.edu/biology/2 This Article is brought to you for free and open access by the College of Arts and Sciences at Digital Commons @ ACU. It has been accepted for inclusion in Biology by an authorized administrator of Digital Commons @ ACU. Syst. Biol. 67(2):236–249, 2018 © The Author(s) 2017. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For Permissions, please email: [email protected] DOI:10.1093/sysbio/syx070 Advance Access publication August 26, 2017 Conflicting Evolutionary Histories of the Mitochondrial and Nuclear Genomes in New World Myotis Bats ROY N. PLATT II1,BRANT C. FAIRCLOTH2,KEVIN A. M. SULLIVAN1,TROY J. KIERAN3,TRAVIS C. GLENN3,MICHAEL W. ,∗ VANDEWEGE1,THOMAS E. -
Bite Force, Cranial Morphometrics and Size in the Fishing Bat Myotis Vivesi (Chiroptera: Vespertilionidae)
Bite force, cranial morphometrics and size in the fishing bat Myotis vivesi (Chiroptera: Vespertilionidae) Sandra M. Ospina-Garcés1,2, Efraín De Luna3, L. Gerardo Herrera M.4, Joaquín Arroyo-Cabrales5, & José Juan Flores-Martínez6 1. Posgrado en Ciencias Biológicas, Instituto de Biología, Universidad Nacional Autónoma de México, Apartado Postal 70-153, 04510 México, Distrito Federal; [email protected] https://orcid.org/0000-0002-0950-4390 2. Instituto de Ecología, A.C. Carretera Antigua a Coatepec 351, El Haya, Xalapa, 91070, México, [email protected]; https://orcid.org/0000-0002-0950-4390 3. Instituto de Ecología A.C. Biodiversidad y Sistemática, Xalapa, Veracruz, 91070; [email protected], https:// orcid.org/0000-0002-6198-3501 4. Estación de Biología de Chamela, Instituto de Biología, Universidad Nacional Autónoma de México, Apartado Postal 21, San Patricio, Jalisco, 48980, México; [email protected] 5. Laboratorio de Arqueozoología, ‘M. en C. Ticul Álvarez Solórzano’ INAH, Moneda # 16 Col. Centro, 06060 México, Distrito Federal; [email protected] 6. Laboratorio de Sistemas de Información Geográfica, Departamento de Zoología. Instituto de Biología, Universidad Nacional Autónoma de México, Circuito Exterior, Edificio Nuevo, Módulo C, Apartado Postal 70-153, 04510 México, Distrito Federal; [email protected] * Correspondence Received 06-IV-2018. Corrected 31-VII-2018. Accepted 18-IX-2018. Abstract: Fish-eating in bats evolved independently in Myotis vivesi (Vespertillionidae) and Noctilio leporinus (Noctilionidae). We compared cranial morphological characters and bite force between these species to test the existence of evolutionary parallelism in piscivory. We collected cranial distances of M. vivesi, two related insectivorous bats (M. velifer and M. -
The Australasian Bat Society Newsletter
The Australasian Bat Society Newsletter Number 29 November 2007 ABS Website: http://abs.ausbats.org.au ABS Listserver: http://listserv.csu.edu.au/mailman/listinfo/abs ISSN 1448-5877 The Australasian Bat Society Newsletter, Number 29, November 2007 – 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: 31st March for the April issue, and 31st 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. Please use the Microsoft Word template if you can (available from the editor). 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. -
Species Assessment for Fringed Myotis (Myotis Thysanodes ) in Wyoming
SPECIES ASSESSMENT FOR FRINGED MYOTIS (MYOTIS THYSANODES ) IN WYOMING prepared by DOUGLAS A. KEINATH Zoology Program Manager, Wyoming Natural Diversity Database, University of Wyoming, 1000 E. University Ave, Dept. 3381, Laramie, Wyoming 82071; 307-766-3013; [email protected] prepared for United States Department of the Interior Bureau of Land Management Wyoming State Office Cheyenne, Wyoming December 2003 Keinath - Myotis thysanodes December 2003 Table of Contents SUMMARY .......................................................................................................................................... 3 INTRODUCTION ................................................................................................................................. 3 NATURAL HISTORY ........................................................................................................................... 5 Morphological Description ...................................................................................................... 5 Taxonomy and Distribution ..................................................................................................... 6 Taxonomy .......................................................................................................................................6 Range...............................................................................................................................................7 Abundance.......................................................................................................................................8 -
Fringed Myotis Myotis Thysanodes
Wyoming Species Account Fringed Myotis Myotis thysanodes REGULATORY STATUS USFWS: No special status USFS R2: Sensitive USFS R4: No special status Wyoming BLM: Sensitive State of Wyoming: Nongame Wildlife CONSERVATION RANKS USFWS: No special status WGFD: NSS3 (Bb), Tier II WYNDD: G4, S2S3 Wyoming Contribution: LOW IUCN: Least Concern STATUS AND RANK COMMENTS The Wyoming Natural Diversity Database (WYNDD) has assigned Fringed Myotis (Myotis thysanodes) a range of state conservation ranks because of uncertainty in the population trend of the species in Wyoming. NATURAL HISTORY Taxonomy: There are three recognized subspecies of Fringed Myotis, with some researchers recognizing a fourth 1-3. Two subspecies occur in Wyoming with M. t. thysanodes found across most of the state. A unique subspecies, M. t. pahasapensis is found in the Black Hills of northeastern Wyoming 3. Description: Identification of Fringed Myotis is possible in the field by experienced observers. Fringed Myotis is a medium-sized bat overall but large among Myotis species. Pelage color varies across the species’ range. Dorsal fur ranges from yellow-brown to dark olive-brown. Ventral fur is similar in coloration but paler. Appearance of M. t. pahasapensis in the Black Hills is unique. Dorsally, the subspecies is brown ochraceous buff and ventrally it is light ochraceous buff 4. The ears are long (16–20 mm) and very dark in color with a long tragus 3, 5. Wing and tail membranes are very dark and nearly opaque 5, 6. Females are significantly larger than males but are otherwise identical in appearance 3. Juveniles are indistinguishable from adults by around 21 days of age except for open epiphyseal closures 4. -
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. -
Chiropterology Division BC Arizona Trial Event 1 1. DESCRIPTION: Participants Will Be Assessed on Their Knowledge of Bats, With
Chiropterology Division BC Arizona Trial Event 1. DESCRIPTION: Participants will be assessed on their knowledge of bats, with an emphasis on North American Bats, South American Microbats, and African MegaBats. A TEAM OF UP TO: 2 APPROXIMATE TIME: 50 minutes 2. EVENT PARAMETERS: a. Each team may bring one 2” or smaller three-ring binder, as measured by the interior diameter of the rings, containing information in any form and from any source. Sheet protectors, lamination, tabs and labels are permitted in the binder. b. If the event features a rotation through a series of stations where the participants interact with samples, specimens or displays; no material may be removed from the binder throughout the event. c. In addition to the binder, each team may bring one unmodified and unannotated copy of either the National Bat List or an Official State Bat list which does not have to be secured in the binder. 3. THE COMPETITION: a. The competition may be run as timed stations and/or as timed slides/PowerPoint presentation. b. Specimens/Pictures will be lettered or numbered at each station. The event may include preserved specimens, skeletal material, and slides or pictures of specimens. c. Each team will be given an answer sheet on which they will record answers to each question. d. No more than 50% of the competition will require giving common or scientific names. e. Participants should be able to do a basic identification to the level indicated on the Official List. States may have a modified or regional list. See your state website. -
Anatomical Diversification of a Skeletal Novelty in Bat Feet
ORIGINAL ARTICLE doi:10.1111/evo.13786 Anatomical diversification of a skeletal novelty in bat feet Kathryn E. Stanchak,1,2 Jessica H. Arbour,1 and Sharlene E. Santana1 1Department of Biology and Burke Museum of Natural History and Culture, University of Washington, Seattle, Washington 98195 2E-mail: [email protected] Received December 21, 2018 Accepted May 18, 2019 Neomorphic, membrane-associated skeletal rods are found in disparate vertebrate lineages, but their evolution is poorly under- stood. Here we show that one of these elements—the calcar of bats (Chiroptera)—is a skeletal novelty that has anatomically diversified. Comparisons of evolutionary models of calcar length and corresponding disparity-through-time analyses indicate that the calcar diversified early in the evolutionary history of Chiroptera, as bats phylogenetically diversified after evolving the capac- ity for flight. This interspecific variation in calcar length and its relative proportion to tibia and forearm length is of functional relevance to flight-related behaviors. We also find that the calcar varies in its tissue composition among bats, which might affect its response to mechanical loading. We confirm the presence of a synovial joint at the articulation between the calcar and the cal- caneus in some species, which suggests the calcar has a kinematic functional role. Collectively, this functionally relevant variation suggests that adaptive advantages provided by the calcar led to its anatomical diversification. Our results demonstrate that novel skeletal additions can become integrated into vertebrate body plans and subsequently evolve into a variety of forms, potentially impacting clade diversification by expanding the available morphological space into which organisms can evolve. -
Echolocation and Foraging Behavior of the Lesser Bulldog Bat, Noctilio Albiventris : Preadaptations for Piscivory?
Behav Ecol Sociobiol (1998) 42: 305±319 Ó Springer-Verlag 1998 Elisabeth K. V. Kalko á Hans-Ulrich Schnitzler Ingrid Kaipf á Alan D. Grinnell Echolocation and foraging behavior of the lesser bulldog bat, Noctilio albiventris : preadaptations for piscivory? Received: 21 April 1997 / Accepted after revision: 12 January 1998 Abstract We studied variability in foraging behavior of can be interpreted as preadaptations favoring the evo- Noctilio albiventris (Chiroptera: Noctilionidae) in Costa lution of piscivory as seen in N. leporinus. Prominent Rica and Panama and related it to properties of its among these specializations are the CF components of echolocation behavior. N. albiventris searches for prey in the echolocation signals which allow detection and high (>20 cm) or low (<20 cm) search ¯ight, mostly evaluation of ¯uttering prey amidst clutter-echoes, high over water. It captures insects in mid-air (aerial cap- variability in foraging strategy and the associated tures) and from the water surface (pointed dip). We once echolocation behavior, as well as morphological spe- observed an individual dragging its feet through the cializations such as enlarged feet for capturing prey from water (directed random rake). In search ¯ight, N. al- the water surface. biventris emits groups of echolocation signals (duration 10±11 ms) containing mixed signals with constant-fre- Key words Bats á Echolocation á Foraging á quency (CF) and frequency-modulated (FM) compo- Evolution á Piscivory nents, or pure CF signals. Sometimes, mostly over land, it produces long FM signals (duration 15±21 ms). When N. albiventris approaches prey in a pointed dip or in aerial captures, pulse duration and pulse interval are Introduction reduced, the CF component is eliminated, and a termi- nal phase with short FM signals (duration 2 ms) at high The development of ¯ight and echolocation give bats repetition rates (150±170 Hz) is emitted. -
The Evolution of Echolocation in Bats: a Comparative Approach
The evolution of echolocation in bats: a comparative approach Alanna Collen A thesis submitted for the degree of Doctor of Philosophy from the Department of Genetics, Evolution and Environment, University College London. November 2012 Declaration Declaration I, Alanna Collen (née Maltby), confirm that the work presented in this thesis is my own. Where information has been derived from other sources, this is indicated in the thesis, and below: Chapter 1 This chapter is published in the Handbook of Mammalian Vocalisations (Maltby, Jones, & Jones) as a first authored book chapter with Gareth Jones and Kate Jones. Gareth Jones provided the research for the genetics section, and both Kate Jones and Gareth Jones providing comments and edits. Chapter 2 The raw echolocation call recordings in EchoBank were largely made and contributed by members of the ‘Echolocation Call Consortium’ (see full list in Chapter 2). The R code for the diversity maps was provided by Kamran Safi. Custom adjustments were made to the computer program SonoBat by developer Joe Szewczak, Humboldt State University, in order to select echolocation calls for measurement. Chapter 3 The supertree construction process was carried out using Perl scripts developed and provided by Olaf Bininda-Emonds, University of Oldenburg, and the supertree was run and dated by Olaf Bininda-Emonds. The source trees for the Pteropodidae were collected by Imperial College London MSc student Christina Ravinet. Chapter 4 Rob Freckleton, University of Sheffield, and Luke Harmon, University of Idaho, helped with R code implementation. 2 Declaration Chapter 5 Luke Harmon, University of Idaho, helped with R code implementation. Chapter 6 Joseph W. -
Characterizing Summer Roosts of Male Little Brown Myotis (Myotis Lucifugus)
CHARACTERIZING SUMMER ROOSTS OF MALE LITTLE BROWN MYOTIS (MYOTIS LUCIFUGUS) IN LODGEPOLE PINE-DOMINATED FORESTS by Shannon Lauree Hilty A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Fish and Wildlife Management MONTANA STATE UNIVERSITY Bozeman, Montana May 2020 ©COPYRIGHT by Shannon Lauree Hilty 2020 All Rights Reserved ii ACKNOWLEDGEMENTS I would like to thank my mentors, Andrea Litt, Bryce Maxell, Lauri Hanauska- Brown, and Amie Shovlain, as well as my committee members Claire Gower and Robert Garrott, for guiding me through this process. Andrea, thank you for providing direction through the Spartan course that is graduate school and for introducing me to my lab family. Bryce, Amie, and Lauri, thank you for being some of the biggest cheerleaders for Montana’s smallest wildlife groups. Thank you to everyone that helped me in the field, including Brandi Skone, Heather Harris, Cody Rose Brown, Erin Brekstad, Kathi and Hazel Irvine, Wilson and Jane Wright, Katie Carroll, Michael Yarnall, Michael Forzley, Autumn Saunders, Katie Geraci, Rebecca Hamlin-Sharpe, Devin Jones, Olivia Bates, Emma Grusing, and my primary technicians, Jacob Melhuish, Scott Hollis, and Monique Metza. I am grateful to my current employer, Westech Environmental Services. You are a phenomenal group of people, and I am so happy to call you family. I want to thank Montana Fish, Wildlife, and Parks, Montana Natural Heritage Program, USDA Forest Service, Bureau of Land Management, and MPG Ranch for providing funding for this project. I am especially thankful to Alexis McEwan, Boaz Crees, Scott Blum, Dan Bachen, Braden Burkholder, and Karen Coleman for offering expertise, gear, and logistical support to my field team. -
Redalyc. Bite Force, Cranial Morphometrics and Size in The
Revista de Biología Tropical ISSN: 0034-7744 [email protected] Universidad de Costa Rica Costa Rica Ospina-Garcés, Sandra M.; De Luna, Efraín; Herrera M., L. Gerardo; Arroyo-Cabrales, Joaquín; Flores-Martínez, José Juan Bite force, cranial morphometrics and size in the fishing bat Myotis vivesi (Chiroptera: Vespertilionidae) Revista de Biología Tropical, vol. 66, núm. 4, diciembre, 2018, pp. 1614-1628 Universidad de Costa Rica San Pedro de Montes de Oca, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44959684023 Abstract Fish-eating in bats evolved independently in Myotis vivesi (Vespertillionidae) and Noctilio leporinus (Noctilionidae). We compared cranial morphological characters and bite force between these species to test the existence of evolutionary parallelism in piscivory. We collected cranial distances of M. vivesi, two related insectivorous bats (M. velifer and M. keaysi), two facultatively piscivorous bats (M. daubentonii and M. capaccinii), and N. leporinus. We analyzed morphometric data applying multivariate methods to test for differences among the six species. We also measured bite force in M. vivesi and evaluated if this value was well predicted by its cranial size. Both piscivorous species were morphologically different from the facultatively piscivorous and insectivorous species, and skull size had a significant contribution to this difference. However, we did not find morphological and functional similarities that could be interpreted as parallelisms between M. vivesi and N. leporinus. These two piscivorous species differed significantly in cranial measurements and in bite force. Bite force measured for M. vivesi was well predicted by skull size. Piscivory in M. vivesi might be associated to the existence of a vertically displaced temporal muscle and an increase in gape angle that allows a moderate bite force to process food.