Checklist of Rodents and Insectivores of the Mordovia, Russia
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
JVP 26(3) September 2006—ABSTRACTS
Neoceti Symposium, Saturday 8:45 acid-prepared osteolepiforms Medoevia and Gogonasus has offered strong support for BODY SIZE AND CRYPTIC TROPHIC SEPARATION OF GENERALIZED Jarvik’s interpretation, but Eusthenopteron itself has not been reexamined in detail. PIERCE-FEEDING CETACEANS: THE ROLE OF FEEDING DIVERSITY DUR- Uncertainty has persisted about the relationship between the large endoskeletal “fenestra ING THE RISE OF THE NEOCETI endochoanalis” and the apparently much smaller choana, and about the occlusion of upper ADAM, Peter, Univ. of California, Los Angeles, Los Angeles, CA; JETT, Kristin, Univ. of and lower jaw fangs relative to the choana. California, Davis, Davis, CA; OLSON, Joshua, Univ. of California, Los Angeles, Los A CT scan investigation of a large skull of Eusthenopteron, carried out in collaboration Angeles, CA with University of Texas and Parc de Miguasha, offers an opportunity to image and digital- Marine mammals with homodont dentition and relatively little specialization of the feeding ly “dissect” a complete three-dimensional snout region. We find that a choana is indeed apparatus are often categorized as generalist eaters of squid and fish. However, analyses of present, somewhat narrower but otherwise similar to that described by Jarvik. It does not many modern ecosystems reveal the importance of body size in determining trophic parti- receive the anterior coronoid fang, which bites mesial to the edge of the dermopalatine and tioning and diversity among predators. We established relationships between body sizes of is received by a pit in that bone. The fenestra endochoanalis is partly floored by the vomer extant cetaceans and their prey in order to infer prey size and potential trophic separation of and the dermopalatine, restricting the choana to the lateral part of the fenestra. -
PLAGUE STUDIES * 6. Hosts of the Infection R
Bull. Org. mond. Sante 1 Bull. World Hlth Org. 1952, 6, 381-465 PLAGUE STUDIES * 6. Hosts of the Infection R. POLLITZER, M.D. Division of Epidemiology, World Health Organization Manuscript received in April 1952 RODENTS AND LAGOMORPHA Reviewing in 1928 the then rather limited knowledge available concerning the occurrence and importance of plague in rodents other than the common rats and mice, Jorge 129 felt justified in drawing a clear-cut distinction between the pandemic type of plague introduced into human settlements and houses all over the world by the " domestic " rats and mice, and " peste selvatique ", which is dangerous for man only when he invades the remote endemic foci populated by wild rodents. Although Jorge's concept was accepted, some discussion arose regarding the appropriateness of the term " peste selvatique" or, as Stallybrass 282 and Wu Lien-teh 318 translated it, " selvatic plague ". It was pointed out by Meyer 194 that, on etymological grounds, the name " sylvatic plague " would be preferable, and this term was widely used until POzzO 238 and Hoekenga 105 doubted, and Girard 82 denied, its adequacy on the grounds that the word " sylvatic" implied that the rodents concerned lived in forests, whereas that was rarely the case. Girard therefore advocated the reversion to the expression "wild-rodent plague" which was used before the publication of Jorge's study-a proposal it has seemed advisable to accept for the present studies. Much more important than the difficulty of adopting an adequate nomenclature is that of distinguishing between rat and wild-rodent plague- a distinction which is no longer as clear-cut as Jorge was entitled to assume. -
Ecological Distribution of Sagebrush Voles, Lagurus Curtatus, in South-Central Washington Author(S): Thomas P
American Society of Mammalogists Ecological Distribution of Sagebrush Voles, Lagurus curtatus, in South-Central Washington Author(s): Thomas P. O'Farrell Source: Journal of Mammalogy, Vol. 53, No. 3 (Aug., 1972), pp. 632-636 Published by: American Society of Mammalogists Stable URL: http://www.jstor.org/stable/1379063 . Accessed: 28/08/2013 16:58 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. American Society of Mammalogists is collaborating with JSTOR to digitize, preserve and extend access to Journal of Mammalogy. http://www.jstor.org This content downloaded from 128.193.8.24 on Wed, 28 Aug 2013 16:58:33 PM All use subject to JSTOR Terms and Conditions 632 JOURNAL OF MAMMALOGY Vol. 53, No. 3 curved needle. After perfusion with penicillin G, the second incision was closed. The base of the plug was slipped into the first incision and sutured to the lumbodorsal fascia with 5-0 Mersilene (Ethicon). After perfusion around the plug with penicillin G, the skin was sutured around the narrow neck of the plug and the incision was dusted with antibiotic powder. The bat could be lifted by the plug with no apparent discomfort and no distortion of the skin or damage to the electrodes. -
Decayed Trees As Resting Places for Japanese Dormouse, Glirulus Japanicus During the Active Period
Decayed trees as resting places for Japanese dormouse, Glirulus japanicus during the active period HARUKA AIBA, MANAMI IWABUCHI, CHISE MINATO, ATUSHI KASHIMURA, TETSUO MORITA AND SHUSAKU MINATO Keep Dormouse Museum, 3545 Kiyosato, Takane-cho, Hokuto-city, Yamanashi, 407-0301, Japan Decayed trees were surveyed for their role as a resting place for non-hibernating dormice at two sites, at southwest of Mt. Akadake in Yamanashi Prefecture (35°56’N, 138°25’E). A telemeter located three dormice, which frequently used decayed trees in the daytime, with two at more than 50% of the times. The survey also showed decayed trees made up only about one fourth of all trees present in various conditions in habitat forests. These two data indicated that decayed trees are an important resting place for non-hibernating dormice in the daytime and provide favorable environmental conditions for inhabitation. Using national nut hunt surveys to find protect and raise the profile of hazel dormice throughout their historic range NIDA AL FULAIJ People’s Trust for Endangered Species (list of authors to come) The first Great Nut Hunt (GNH), launched in 1993 had 6500 participants, identifying 334 new sites and thus confirming the presence of dormice in 29 counties in England and Wales. In 2001, 1200 people found 136 sites with positive signs of hazel dormice. The third GNH started in 2009. Over 4000 people registered and to date almost 460 woodland or hedgerow surveys have been carried out, in conjunction with a systematic survey of 286 woodlands on the Isle of Wight. Of the 460 surveys carried out by the general public, 74 found evidence of dormice. -
Diet and Microhabitat Use of the Woodland Dormouse Graphiurus Murinus at the Great Fish River Reserve, Eastern Cape, South Africa
Diet and microhabitat use of the woodland dormouse Graphiurus murinus at the Great Fish River Reserve, Eastern Cape, South Africa by Siviwe Lamani A dissertation submitted in fulfilment of the requirements for the degree of MASTER OF SCIENCE (ZOOLOGY) in the Faculty of Science and Agriculture at the University of Fort Hare 2014 Supervisor: Ms Zimkitha Madikiza Co-supervisor: Prof. Emmanuel Do Linh San DECLARATION I Siviwe Lamani , student number 200604535 hereby declare that this dissertation titled “Diet and microhabitat use of the woodland dormouse Graphiurus murinus at the Great Fish River Reserve , Eastern Cape, South Africa” submitted for the award of the Master of Science degree in Zoology at the University of Fort Hare, is my own work that has never been submitted for any other degree at this university or any other university. Signature: I Siviwe Lamani , student number 200604535 hereby declare that I am fully aware of the University of Fort Hare policy on plagiarism and I have taken every precaution on complying with the regulations. Signature: I Siviwe Lamani , student number 200604535 hereby declare that I am fully aware of the University of Fort Hare policy on research ethics and have taken every precaution to comply with the regulations. The data presented in this dissertation were obtained in the framework of another project that was approved by the University Ethics committee on 31 May 2013 and is covered by the ethical clearance certificate # SAN05 1SGB02. Signature: ii SUPERVISOR’S FOREWORD The format of this Master’s dissertation (abstract, general introduction and two independent papers) has been chosen with two purposes in mind: first, to train the MSc candidate to the writing of scientific papers, and second, to secure and allow for a quicker dissemination of the scientific knowledge. -
Lagurus Curtatus
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by DigitalCommons@University of Nebraska University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Mammalogy Papers: University of Nebraska State Museum Museum, University of Nebraska State April 1980 Lagurus curtatus Lynn E. Carroll CARNEGIE MUSEUM OF NATURAL HISTORY, PITTSBURGH, PENNSYLVANIA 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 Carroll, Lynn E. and Genoways, Hugh H., "Lagurus curtatus" (1980). Mammalogy Papers: University of Nebraska State Museum. 90. https://digitalcommons.unl.edu/museummammalogy/90 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. MAMMALIANSPECIES No. 124, pp. 14,sfigs. Lag~lrU~~~I'tatus. By Lynn E. Carroll and Hugh H. Genorays Published 15 April 1980 by The American Society of Mammalogists Lagurus Gloger, 184 1 dian triangks (Fig. 1); cement present in the reentrant angles of molars; antitragus present; ears over one-half the length of the Laguru Gloger, 1841:97. Type species Lagurus migratorius Glo- hind foot; conspicuous dorsal stripe absent. Its pale coloration, ger (=Mu lagurus Pallas). short tail (about the same length as the hind foot), large bullae, Eremiomys Poliakoff, 1881:34. Type species Mu laguru Pallas. and the structure of the m3 distinguish it from other North Amer- Lemmiscus- Thomas, 1912:401. -
The Genome of the Pyrenean Desman and the Effects of Bottlenecks and Inbreeding on the Genomic Landscape of an Endangered Species
Received: 18 August 2020 | Revised: 19 March 2021 | Accepted: 27 April 2021 DOI: 10.1111/eva.13249 ORIGINAL ARTICLE The genome of the Pyrenean desman and the effects of bottlenecks and inbreeding on the genomic landscape of an endangered species Lídia Escoda | Jose Castresana Institute of Evolutionary Biology (CSIC- Universitat Pompeu Fabra), Barcelona, Spain Abstract The Pyrenean desman (Galemys pyrenaicus) is a small semiaquatic mammal endemic Correspondence Jose Castresana, Institute of Evolutionary to the Iberian Peninsula. Despite its limited range, this species presents a strong ge- Biology (CSIC- Universitat Pompeu Fabra), netic structure due to past isolation in glacial refugia and subsequent bottlenecks. Passeig Marítim de la Barceloneta 37, 08003 Barcelona, Spain. Additionally, some populations are highly fragmented today as a consequence of river Email: [email protected] barriers, causing substantial levels of inbreeding. These features make the Pyrenean Funding information desman a unique model in which to study the genomic footprints of differentiation, Plan Nacional I+D+i del Ministerio de bottlenecks and extreme isolation in an endangered species. To understand these Ciencia e Innovación, Grant/Award Number: CGL2017- 84799- P (MINECO/AEI/FEDER, UE) processes, the complete genome of the Pyrenean desman was sequenced and as- sembled using a Bloom filter- based approach. An analysis of the 1.83 Gb reference genome and the sequencing of five additional individuals from different evolutionary units allowed us to detect its main genomic characteristics. The population differen- tiation of the species was reflected in highly distinctive demographic trajectories. In addition, a severe population bottleneck during the postglacial recolonization of the eastern Pyrenees created one of the lowest genomic heterozygosity values recorded in a mammal. -
The Status and Distribution of Mediterranean Mammals
THE STATUS AND DISTRIBUTION OF MEDITERRANEAN MAMMALS Compiled by Helen J. Temple and Annabelle Cuttelod AN E AN R R E IT MED The IUCN Red List of Threatened Species™ – Regional Assessment THE STATUS AND DISTRIBUTION OF MEDITERRANEAN MAMMALS Compiled by Helen J. Temple and Annabelle Cuttelod The IUCN Red List of Threatened Species™ – Regional Assessment The designation of geographical entities in this book, and the presentation of material, do not imply the expression of any opinion whatsoever on the part of IUCN or other participating organizations, concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland and Cambridge, UK Copyright: © 2009 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Red List logo: © 2008 Citation: Temple, H.J. and Cuttelod, A. (Compilers). 2009. The Status and Distribution of Mediterranean Mammals. Gland, Switzerland and Cambridge, UK : IUCN. vii+32pp. ISBN: 978-2-8317-1163-8 Cover design: Cambridge Publishers Cover photo: Iberian lynx Lynx pardinus © Antonio Rivas/P. Ex-situ Lince Ibérico All photographs used in this publication remain the property of the original copyright holder (see individual captions for details). -
Status of Birds of Oak Creek Wildlife Area
Status of Birds of Oak Creek Wildlife Area Abundance Seasonal Occurance *Species range included in C = Common r= Resident Oak Creek WLA but no U = Uncommon s = Summer Visitor documentation of species R = Rare w= Winter Visitor m=Migrant Common Name Genus Species Status Common Loon* Gavia immer Rw Pied-billed Grebe Podilymbus podiceps Cr Horned Grebe Podiceps auritus Um Eared Grebe Podiceps nigricollis Us Western Grebe Aechmorphorus occidentalis Us Clark's Grebe* Aechmorphorus clarkii Rm Double-crested Cormorant Phalocrorax auritus Um American Bittern* Botaurus lentiginosus Us Great Blue Heron Arden herodias Cr Black-crowned Night-Heron Nycticorax nycticorax Cr Tundra Swan Cygnus columbiaus Rw Trumpeter Swan Cygnus buccinator Am Greater White-fronted Anser albifrons Rm Goose* Snow Goose Chen caerulescens Rw Canada Goose Branta canadensis Cr Green-winged Teal Anas crecca Ur Mallard Anas Platyrynchos Cr Northen Pintail Anas acuta Us Blue-winged Teal Anas discors Rm Cinnamon Teal Anas cyanoptera Us Northern Shoveler Anas clypeata Cr Gadwall* Anas strepere Us Eurasian Wigeon* Anas Penelope Rw American Wigeon Anas Americana Cr Wood Duck Aix sponsa Ur Redhead Aythya americana Uw Canvasback Aythya valisineria Uw Ring-necked Duck Aythya collaris Uw Greater Scaup* Aythya marila Rw Leser Scaup Aythya affinis Uw Common Goldeneye Bucephala clangula Uw Barrow's Goldeneye Bucephala islandica Rw Bufflehead Bucephala albeola Cw Harlequin Duck Histrionicus histrionicus Rs White-winged Scoter Melanitta fusca Rm Hooded Merganser Lophodytes Cucullatus Rw -
G-, C-, and NOR-Stained Karyotype of the Eversmann's Hamster Allocricetulus Eversmanni and Comparison with the Karyotype of Cr
Mammal Study 30: 89–91 (2005) © the Mammalogical Society of Japan Short communication G-, C-, and NOR-stained karyotype of the Eversmann’s hamster Allocricetulus eversmanni and comparison with the karyotype of Cricetulus species (Rodentia: Cricetinae) Irina V. Kartavtseva1,* and Aleksey V. Surov2 1 Institute of Biology and Soil Science, Far East Branch of Russian Academy of Sciences, Vladivostok, Russia, 690022 2 A. N. Severtsov Institute of Ecology and Evolution, Moscow, Russia, 119071 Differential chromosomal stainings for various species chromosomes was shown using Sumner’s (1972) modi- belonging to genera in the tribe Cricetini of the Eurasian fied C-banding technique. The locations of nucleolar Cricetinae including Cricetus, Cricetulus, Tscherskia, organizer regions (NORs) of metaphase chromosomes Phodopus, and Mesocricetus are available (Gamperl et were determined after 50% aqueous AgNO3 treatment al. 1978; Kartavtseva et al. 1979; Popescu and DiPaolo for 12 hours at 50–60°C (Bloom and Goodpasture 1976). 1980; Kral et al. 1984). Hitherto, however, no differen- The karyotype consisted of 24 autosomes (2n = 26, tial chromosomes stainings for species in the genus NF = 40): four pairs of metacentrics (M) and submeta- Allocricetulus have been described and the phylogenetic centrics (SM): one pair large, one pair medium and two position of this genus in the Cricetini, based on chro- pairs small, two pairs of large subtelocentrics (ST) and mosomal data, has not been determined. six pairs of acrocentrics (A), ranging from medium-sized The Eversmann’s hamster Allocricetus eversmanni to small. The X chromosome was a medium sized sub- Brandt, 1859 occurs in dry steppes and semi-deserts metacentric (Fig. -
On the Original Description of the Sacred Shrew, Sorex Religiosa I. Geoffroy Saint-Hilaire, 1826 [Nec 1827] (Mammalia: Soricidae)
Bionomina, 9: 50–53 (2015) ISSN 1179-7649 (print edition) www.mapress.com/bionomina/ Article BIONOMINA Copyright © 2015 • Magnolia Press ISSN 1179-7657 (online edition) http://dx.doi.org/10.11646/bionomina.9.1.5 http://zoobank.org/urn:lsid:zoobank.org:pub:790065A5-5351-4E9F-9BA6-6A4F9B10BEC0 On the original description of the Sacred Shrew, Sorex religiosa I. Geoffroy Saint-Hilaire, 1826 [nec 1827] (Mammalia: Soricidae) Neal WOODMAN USGS Patuxent Wildlife Research Center, MRC-111, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, D.C. 20013-7012, U.S.A. <[email protected]> Abstract The original description of the Egyptian Pygmy Shrew or Sacred Shrew, Sorex religiosus I. Geoffroy Saint-Hilaire (Mammalia: Soricidae: Crocidura religiosa), was based on mummies obtained by Joseph Passalacqua from the ancient Egyptian necropolis at Thebes, Egypt. The description and naming of this species is commonly credited to Geoffroy Saint-Hilaire’s (1827) compendium and review of shrews in the Mémoires du Muséum d’Histoire naturelle. However, this author also described this species in two earlier publications. The first was in a footnote to Passalacqua’s (1826) Catalogue raisonné et historique des antiquités découvertes en Égypte; the second in January 1827 in the 11th volume of the Dictionnaire classique d’Histoire naturelle. In each case, he explained what he considered to be the distinguishing characteristics of the species and presented its common and scientific names. Priority, therefore, goes to Geoffroy Saint- Hilaire’s description in Passalacqua’s (1826) Catalogue. Key words: Insectivora, Sorex, Crocidura, mummy, systematics, taxonomy Introduction The Egyptian Pygmy Shrew or Sacred Shrew, Sorex religiosus I. -
Species Examined.Xlsx 8:17 PM 5/31/2011
8:17 PM 5/31/2011 Names Accepted Binomial Name, Family Page Binomial Name, Page Common Name as of 2011, as given in Sperber if different than in Sperber Monotremata 264 Duckbilled Platypus Ornithorhynchus anatinus 264 Marsupialia 266 Slender‐tailed Dunnart Sminthopsis murina 266 Kultarr Antechinomys laniger 268 Gray Four‐eyed Opossum Philander opossum Didelphys opossum 269 (or possibly Virginia Opossum) ( or Didelphis virginiana) Eastern Grey Kangaroo Macropus giganteus 269 Insectivora 272 Elephant Shrew Macroscelides sp. 272 Hedgehog Erinaceus europaeus 273 Eurasian Pygmy Shrew Sorex minutus 274 Eurasian Water Shrew Neomys fodiens 279 Pygmy White Toothed Suncus etruscus Pachyura etrusca 280 (or Etruscan ) Shrew Russian Desman Desmana moschata 280 Chiroptera 281 Greater Flying Fox Pteropus vampyrus Pteropus edulis 281 (Kalong, Kalang) Northern Bat Eptesicus nilssonii Pipistrellus nilssoni 283 Particoloured Bat Vespertilio murinus 285 Xenarthra 287 and Pholidota Armadillos, anteaters and pangolins: Review of the literature only Rodentia 288 European Rabbit Oryctolagus cuniculus 288 Eurasian Red Squirrel Sciurus vulgaris 293 Eurasian Beaver Castor fiber 294 Agile Kangaroo Rats Dipodomys agilis Perodipus agilis 296 Fresno Kangaroo Rat Dipodomys nitratoides exilis Dipodomys meriami exilis 297 Lesser Egyptian Jerboa Jaculus jaculus 298 Field (or Short‐tailed) Vole Microtus agrestis 299 Bank Vole Myodes glareolus Evotomys glareolus 303 European (or Northern) Water Arvicola terrestris 303 Vole Black Rat Rattus Rattus Epimys rattus 303 House Mouse