Sorex Hoyi Hoyi, Pygmy Shrew
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Pacific Water Shrew Sorex Bendirii
COSEWIC Assessment and Update Status Report on the Pacific Water Shrew Sorex bendirii in Canada ENDANGERED 2006 COSEWIC COSEPAC COMMITTEE ON THE STATUS OF COMITÉ SUR LA SITUATION ENDANGERED WILDLIFE DES ESPÈCES EN PÉRIL IN CANADA AU CANADA COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows: COSEWIC 2006. COSEWIC assessment and update status report on the Pacific watershrew Sorex bendirii in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vi + 28 pp. (www.sararegistry.gc.ca/status/status_e.cfm). Previous report: Galindo-Leal, C. and J.B. Runciman. 1994. COSEWIC status report on the Pacific water shrew Sorex bendirii in Canada. Committee on the Status of Endangered Wildlife in Canada. 1-33 pp. Production note: COSEWIC would like to acknowledge David Nagorsen for writing the update status report on the Pacific water shrew Sorex bendirii, prepared under contract with Environment Canada, and overseen and edited by Mark Brigham, Co-chair (Terrestrial Mammals), COSEWIC Terrestrial Mammals Species Specialist Subcommittee. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: (819) 997-4991 / (819) 953-3215 Fax: (819) 994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Également disponible en français sous le titre Évaluation et Rapport de situation du COSEPAC sur la musaraigne de Bendire (Sorex bendirii) au Canada – Mise à jour. Cover illustration: Pacific water shrew – by Ron Altig. ©Her Majesty the Queen in Right of Canada 2006 Catalogue No. -
Mammal Species Native to the USA and Canada for Which the MIL Has an Image (296) 31 July 2021
Mammal species native to the USA and Canada for which the MIL has an image (296) 31 July 2021 ARTIODACTYLA (includes CETACEA) (38) ANTILOCAPRIDAE - pronghorns Antilocapra americana - Pronghorn BALAENIDAE - bowheads and right whales 1. Balaena mysticetus – Bowhead Whale BALAENOPTERIDAE -rorqual whales 1. Balaenoptera acutorostrata – Common Minke Whale 2. Balaenoptera borealis - Sei Whale 3. Balaenoptera brydei - Bryde’s Whale 4. Balaenoptera musculus - Blue Whale 5. Balaenoptera physalus - Fin Whale 6. Eschrichtius robustus - Gray Whale 7. Megaptera novaeangliae - Humpback Whale BOVIDAE - cattle, sheep, goats, and antelopes 1. Bos bison - American Bison 2. Oreamnos americanus - Mountain Goat 3. Ovibos moschatus - Muskox 4. Ovis canadensis - Bighorn Sheep 5. Ovis dalli - Thinhorn Sheep CERVIDAE - deer 1. Alces alces - Moose 2. Cervus canadensis - Wapiti (Elk) 3. Odocoileus hemionus - Mule Deer 4. Odocoileus virginianus - White-tailed Deer 5. Rangifer tarandus -Caribou DELPHINIDAE - ocean dolphins 1. Delphinus delphis - Common Dolphin 2. Globicephala macrorhynchus - Short-finned Pilot Whale 3. Grampus griseus - Risso's Dolphin 4. Lagenorhynchus albirostris - White-beaked Dolphin 5. Lissodelphis borealis - Northern Right-whale Dolphin 6. Orcinus orca - Killer Whale 7. Peponocephala electra - Melon-headed Whale 8. Pseudorca crassidens - False Killer Whale 9. Sagmatias obliquidens - Pacific White-sided Dolphin 10. Stenella coeruleoalba - Striped Dolphin 11. Stenella frontalis – Atlantic Spotted Dolphin 12. Steno bredanensis - Rough-toothed Dolphin 13. Tursiops truncatus - Common Bottlenose Dolphin MONODONTIDAE - narwhals, belugas 1. Delphinapterus leucas - Beluga 2. Monodon monoceros - Narwhal PHOCOENIDAE - porpoises 1. Phocoena phocoena - Harbor Porpoise 2. Phocoenoides dalli - Dall’s Porpoise PHYSETERIDAE - sperm whales Physeter macrocephalus – Sperm Whale TAYASSUIDAE - peccaries Dicotyles tajacu - Collared Peccary CARNIVORA (48) CANIDAE - dogs 1. Canis latrans - Coyote 2. -
Checklist of Rodents and Insectivores of the Mordovia, Russia
ZooKeys 1004: 129–139 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.1004.57359 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research Checklist of rodents and insectivores of the Mordovia, Russia Alexey V. Andreychev1, Vyacheslav A. Kuznetsov1 1 Department of Zoology, National Research Mordovia State University, Bolshevistskaya Street, 68. 430005, Saransk, Russia Corresponding author: Alexey V. Andreychev ([email protected]) Academic editor: R. López-Antoñanzas | Received 7 August 2020 | Accepted 18 November 2020 | Published 16 December 2020 http://zoobank.org/C127F895-B27D-482E-AD2E-D8E4BDB9F332 Citation: Andreychev AV, Kuznetsov VA (2020) Checklist of rodents and insectivores of the Mordovia, Russia. ZooKeys 1004: 129–139. https://doi.org/10.3897/zookeys.1004.57359 Abstract A list of 40 species is presented of the rodents and insectivores collected during a 15-year period from the Republic of Mordovia. The dataset contains more than 24,000 records of rodent and insectivore species from 23 districts, including Saransk. A major part of the data set was obtained during expedition research and at the biological station. The work is based on the materials of our surveys of rodents and insectivo- rous mammals conducted in Mordovia using both trap lines and pitfall arrays using traditional methods. Keywords Insectivores, Mordovia, rodents, spatial distribution Introduction There is a need to review the species composition of rodents and insectivores in all regions of Russia, and the work by Tovpinets et al. (2020) on the Crimean Peninsula serves as an example of such research. Studies of rodent and insectivore diversity and distribution have a long history, but there are no lists for many regions of Russia of Copyright A.V. -
The Preface of “Evolutionary Biology and Phylogeny of the Talpidae”
Mammal Study 30: S3 (2005) © the Mammalogical Society of Japan The preface of “Evolutionary biology and phylogeny of the Talpidae” The symposium “Evolutionary biology and phylogeny pleasure to say “Mission accomplished”! of the Talpidae” was held on the 3rd of August as part of This symposium was accompanied by three poster the IX International Mammalogical Congress (IMC9) in presentations. Dr. N. Sagara presented his new research Sapporo, Japan, 31 July–5 August 2005, and attracted topic, ‘Myco-talpology’, which is the science pertaining about 50 individuals interested in the family Talpidae to the ecological relationships between mushrooms and and other subterranean mammals. moles. Dr. Y. Yokohata communicated his and his After a brief introduction by Dr. Y. Yokohata, Dr. S. student’s research on lesser Japanese moles. The first Kawada highlighted his recent studies on the karyologi- poster examined the social relationships between indi- cal and morphological aspects of the lesser-known Asian vidual moles in captivity, while the second documented mole species, and forwarded several taxonomic prob- and compared the diet of an isolated insular population lems yet to be addressed. Dr. A. Loy followed this (Kinkasan Island) of moles inhabiting a ‘turf’ habitat presentation by discussing the origin and evolutionary altered by high populations of sika deer with those in history of Western European fossorial moles of the genus natural ‘forest’ environments. Talpa based on her and her collaborators’ studies of their In this proceeding, the following -
MAMMALS of WASHINGTON Order DIDELPHIMORPHIA
MAMMALS OF WASHINGTON If there is no mention of regions, the species occurs throughout the state. Order DIDELPHIMORPHIA (New World opossums) DIDELPHIDAE (New World opossums) Didelphis virginiana, Virginia Opossum. Wooded habitats. Widespread in W lowlands, very local E; introduced from E U.S. Order INSECTIVORA (insectivores) SORICIDAE (shrews) Sorex cinereus, Masked Shrew. Moist forested habitats. Olympic Peninsula, Cascades, and NE corner. Sorex preblei, Preble's Shrew. Conifer forest. Blue Mountains in Garfield Co.; rare. Sorex vagrans, Vagrant Shrew. Marshes, meadows, and moist forest. Sorex monticolus, Montane Shrew. Forests. Cascades to coast, NE corner, and Blue Mountains. Sorex palustris, Water Shrew. Mountain streams and pools. Olympics, Cascades, NE corner, and Blue Mountains. Sorex bendirii, Pacific Water Shrew. Marshes and stream banks. W of Cascades. Sorex trowbridgii, Trowbridge's Shrew. Forests. Cascades to coast. Sorex merriami, Merriam's Shrew. Shrub steppe and grasslands. Columbia basin and foothills of Blue Mountains. Sorex hoyi, Pygmy Shrew. Many habitats. NE corner (known only from S Stevens Co.), rare. TALPIDAE (moles) Neurotrichus gibbsii, Shrew-mole. Moist forests. Cascades to coast. Scapanus townsendii, Townsend's Mole. Meadows. W lowlands. Scapanus orarius, Coast Mole. Most habitats. W lowlands, central E Cascades slopes, and Blue Mountains foothills. Order CHIROPTERA (bats) VESPERTILIONIDAE (vespertilionid bats) Myotis lucifugus, Little Brown Myotis. Roosts in buildings and caves. Myotis yumanensis, Yuma Myotis. All habitats near water, roosting in trees, buildings, and caves. Myotis keenii, Keen's Myotis. Forests, roosting in tree cavities and cliff crevices. Olympic Peninsula. Myotis evotis, Long-eared Myotis. Conifer forests, roosting in tree cavities, caves and buildings; also watercourses in arid regions. -
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. -
Small Mammal Survey of the Nulhegan Basin Division of the Silvio 0
Small Mammal Survey of the Nulhegan Basin Division of the Silvio 0. Conte NFWR and the State of Vermont's West Mountain Wildlife Management Area, Essex County Vermont • Final Report March 15, 2001 C. William Kilpatrick Department of Biology University of Vermont Burlington, Vermont 05405-0086 A total of 19 species of small mammals were documented from the Nulhegan Basin Division of the Silvio 0. Conte National Fish and Wildlife Refuge (NFWR) and the West Mountain Wildlife Management Area Seventeen of these species had previously been documented from Essex County, but specimens of the little brown bat (Jr{yotis lucifugu.s) and the northern long-eared bat (M septentrionalis) represent new records for this county. Although no threatened or endangered species were found in this survey, specimens of two rare species were captured including a water shrew (Sorex palustris) and yellow-nosed voles (Microtus chrotorrhinus). Population densities were relatively low as reflected in a mean trap success of 7 %, and the number of captures of two species, the short-tailed shrew (Blarina brevicauda) and the deer mouse (Peromyscus maniculatus), were noticeably low. Low population densities were observed in northern hardwood forests, a lowland spruce-fir forest, a black spruce/dwarf shrub bog, and most clear-cuts, whereas the high population densities were found along talus slopes, in a mixed hardwood forest with some • rock ledges, and in a black spruce swamp. The highest species diversity was found in a montane yellow birch-red spruce forest, a black spruce swamp, a beaver/sedge meadow, and a talus slope within a mixed forest. -
Moles, Shrews, Mice and More
Moles, RESEARCHERS FOCUS IN ON Shrews, NEW HAMPSHIRE’S MANY SMALL Mice MAMMALS and more 8 NovemberSeptember / / December October 2016 2016 by ELLEN SNYDER mall mammals – those weighing less than six ounces – are a surprisingly diverse group. In New England, they include mice, voles, bog lemmings, flying squir- Srels, chipmunks, moles and shrews. Researchers study small mammals because they are common, widespread, diverse, easily handled and reproduce often. My father, Dana Snyder, was one of those researchers. In the 1960s, when I was just four years old, he began a long-term study of the ecology of the eastern chipmunk in the Green Mountains of southern Vermont. Our summer camping trips to his study site infused me with a fondness for small mammals, especially chipmunks. Chipmunks are one of those small mammals that both entertain and annoy. Colorful in their brown and white stripes, they are lively and active during the day. When star- tled, they emit a high-pitched “chip” before darting off to a hideout; their low chuck, chuck, chuck is a common summer sound in our woods. They can stuff huge numbers of seeds into their cheek pouches. Despite their prevalence, chipmunks live solitary lives and are highly territorial. In winter, they take a long nap, waking occasionally to eat stored seeds or emerge above ground on a warm winter day. When I was in elementary school, my dad brought home an orphaned flying squirrel. We were enthralled with its large, dark eyes and soft fur. It would curl up in my shirt pocket, and I took it to school for show-and-tell. -
Northern Short−Tailed Shrew (Blarina Brevicauda)
FIELD GUIDE TO NORTH AMERICAN MAMMALS Northern Short−tailed Shrew (Blarina brevicauda) ORDER: Insectivora FAMILY: Soricidae Blarina sp. − summer coat Credit: painting by Nancy Halliday from Kays and Wilson's Northern Short−tailed Shrews have poisonous saliva. This enables Mammals of North America, © Princeton University Press them to kill mice and larger prey and paralyze invertebrates such as (2002) snails and store them alive for later eating. The shrews have very limited vision, and rely on a kind of echolocation, a series of ultrasonic "clicks," to make their way around the tunnels and burrows they dig. They nest underground, lining their nests with vegetation and sometimes with fur. They do not hibernate. Their day is organized around highly active periods lasting about 4.5 minutes, followed by rest periods that last, on average, 24 minutes. Population densities can fluctuate greatly from year to year and even crash, requiring several years to recover. Winter mortality can be as high as 90 percent in some areas. Fossils of this species are known from the Pliocene, and fossils representing other, extinct species of the genus Blarina are even older. Also known as: Short−tailed Shrew, Mole Shrew Sexual Dimorphism: Males may be slightly larger than females. Length: Range: 118−139 mm Weight: Range: 18−30 g http://www.mnh.si.edu/mna 1 FIELD GUIDE TO NORTH AMERICAN MAMMALS Least Shrew (Cryptotis parva) ORDER: Insectivora FAMILY: Soricidae Least Shrews have a repertoire of tiny calls, audible to human ears up to a distance of only 20 inches or so. Nests are of leaves or grasses in some hidden place, such as on the ground under a cabbage palm leaf or in brush. -
Merriam's Shrew in Nebraska
A-48 MERRIAM’S SHREW Sorex merriami Description Merriam’s shrew has pale gray pelage with whitish feet and white underparts. The tail is bicolored and sparsely haired. The shrew molts in spring and fall. Flank glands are prominent on males during the breeding season, and thought Large compared to to be responsible for the shrew’s strong odor (Armstrong and Jones 1971). other shrews, Johnson and Clanton (1954) suggest this odor may be associated with Merriam’s shrews attracting a mate. are still tiny animals. Merriam’s shrews are large and heavy-bodied relative to shrews that co-occur with them in Colorado (D. Armstrong, pers. comm.), yet they are still tiny animals: total length measures 88 to 107 mm, including tail length of 33 to 42 mm. Adults weigh between 4.4 to 6.5 g (Armstrong and Jones 1971). Distinguishing Merriam’s shrew from other shrews is subtle work; familiarity with shrews in the museum collections is recommended before attempting field identifications (D. Armstrong, pers. com.). Natural history Merriam’s shrews are active at all hours, and like other shrews, often need to and behavior consume more then their body weight in prey per day. The diet consists of spiders, beetles, caterpillars and other small invertebrates, and perhaps vertebrate carrion. Runways and burrows of small rodents are used extensively Merriam’s shrews for foraging (Armstrong and Jones 1971). Runways and burrows of sagebrush are solitary voles are important to Merriam’s shrews in localities where the two species insectivores. Their occur together (Johnson and Clanton 1954). natural history is poorly known. -
Evolution and Postglacial Colonization of Seewis Hantavirus with Sorex Araneus in Finland
Infection, Genetics and Evolution 57 (2018) 88–97 Contents lists available at ScienceDirect Infection, Genetics and Evolution journal homepage: www.elsevier.com/locate/meegid Research paper Evolution and postglacial colonization of Seewis hantavirus with Sorex T araneus in Finland ⁎ Jiaxin Linga, , Teemu Smuraa, Daniel Tamaritb, Otso Huituc, Liina Voutilainena,d, Heikki Henttonend, Antti Vaheria, Olli Vapalahtia,e,f, Tarja Sironena,e a University of Helsinki, Medicum, Department of Virology, Helsinki, Finland b Uppsala University, Biomedical Centre, Science for Life Laboratory, Cell and Molecular Biology, Department of Molecular Evolution, Sweden c Forest and Animal Ecology, Natural Resources Institute Finland, Tampere, Finland d Forest and Animal Ecology, Natural Resources Institute Finland, Helsinki, Finland e University of Helsinki, Department of Veterinary Biosciences, Helsinki, Finland f Helsinki University Hospital, University of Helsinki, Helsinki, Finland ARTICLE INFO ABSTRACT Keywords: Hantaviruses have co-existed with their hosts for millions of years. Seewis virus (SWSV), a soricomorph-borne Hantavirus hantavirus, is widespread in Eurasia, ranging from Central Siberia to Western Europe. To gain insight into the Seewis phylogeography and evolutionary history of SWSV in Finland, lung tissue samples of 225 common shrews (Sorex Sorex araneus araneus) trapped from different parts of Finland were screened for the presence of SWSV RNA. Forty-two of the Evolution samples were positive. Partial small (S), medium (M) and large (L) segments of the virus were sequenced, and Phylogeography analyzed together with all SWSV sequences available in Genbank. The phylogenetic analysis of the partial S- segment sequences suggested that all Finnish SWSV strains shared their most recent common ancestor with the Eastern European strains, while the L-segment suggested multiple introductions. -
The Behavior of Solenodon Paradoxus in Captivity with Comments on the Behavior of Other Insectivora
The Behavior of Solenodon paradoxus in Captivity with Comments on the Behavior of Other Insectivora JOHN F. EISENBERG1 Department of Zoology, University of Maryland & EDWIN GOULD2 Department of Mental Hygiene, Laboratory of Comparative Behavior, Johns Hopkins University (Plates I & II) I. INTRODUCTION For comparative purposes the authors utilized Solenodon paradoxus, confined to the island the extensive collection of living tenrecs main- of Hispaniola, and S. cubanus, endemic to Cuba, tained by Dr. Gould at Johns Hopkins Uni- versity, and drew upon their previous behavioral comprise the sole living members of the family studies of insectivores, which have already been Solenodontidae. A full-grown specimen of S. published in part elsewhere (Eisenberg, 1964; paradoxus may weigh up to 1 kgm. and attain a Gould, 1964, 1965). head and body length of 300 mm. Although large size and primitive molar cusp pattern have led II. SPECIMENS AND MAINTENANCE taxonomists to include this genus with the tenrecs Four specimens of Solenodon paradoxus (one of Madagascar, further morphological studies male, three females) were purchased from a have led certain workers to conclude that Sol- dealer in the Dominican Republic. The male enodon is a primitive soricoid more closely allied (M) and one female (J) were immature and, to the shrews than to the zalambdadont tenrecs extrapolating from their weights (Mohr, 1936 (McDowell, 1958). II), were judged to be four and six months old, The behavior of S. paradoxus was reviewed respectively. The juveniles were studied as a by Dr. Erna Mohr (1936-38). Since her series of pair by Dr. Eisenberg. In addition, all four ani- papers, however, much more has been learned mals were employed in two-animal encounters concerning the behavior of not only the soleno- and were recorded during studies of vocal com- don but also the insectivores of the families munication.