Taxonomic Key to Small Mammals
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Rodent Identification and Signs of Stowaways Key Features of UK Target Rodents
FROM RSPB BIOSECURITY MANUAL CHAPTER 2: RODENT SURVEILLANCE & IDENTIFICATION Rodent identification and signs of stowaways Key features of UK target rodents Black rat Brown rat House mouse FROM RSPB BIOSECURITY MANUAL CHAPTER 2: RODENT SURVEILLANCE & IDENTIFICATION Identifying rodent droppings Rodent droppings can be very variable (depending on diet), including in colour, but as a guide: Brown rat Black rat House mouse -13-19mm long, -7-14mm long -4-8mm long -3-4mm thick -3-4mm thick -2mm thick -Rounded ends, one end may go to -Tapered ends -Small and thin a point (as pictured) -Often slightly curved -A bit like grains of rice -Likely to contain fur -Likely to contain fur -Strong smell of ammonia. -Often located in latrines along tracks, at feeding sites and on prominent rocks Figure 2.9 Droppings of UK invasive rodents. Images: taken from Morton & Cole 2013 Rabbit or goat droppings be mistaken for rat droppings, though they are usually more spherical (particularly rabbit) and uniform. Goat droppings may be more cylindrical but with flatter or round, rather than tapered ends. Breaking up droppings should help (wear gloves): rabbit and goat droppings just contain vegetation, whereas rat droppings are likely to contain fur and a range of food stuffs. Shrew droppings – typically 2-4mm long and 1-2mm thick, these should be smaller than rat or mouse droppings. However, evidence from St Agnes and Gugh (Isles of Scilly) shows shrew droppings can be much larger than this. They are of a sandy consistency and are largely comprised of insect remains, whereas rodent droppings generally contain a wider array of food sources. -
BANDICOTA INDICA, the BANDICOOT RAT 3.1 The
CHAPTER THREE BANDICOTA INDICA, THE BANDICOOT RAT 3.1 The Living Animal 3.1.1 Zoology Rats and mice (family Muridae) are the most common and well-known rodents, not only of the fi elds, cultivated areas, gardens, and storage places but especially so of the houses. Though there are many genera and species, their general appearance is pretty the same. Rats are on average twice as large as mice (see Chapter 31). The bandicoot is the largest rat on the Indian subcontinent, with a body and head length of 30–40 cm and an equally long tail; this is twice as large as the black rat or common house rat (see section 3.1.2 below). This large size immediately distinguishes the bandicoot from other rats. Bandicoots have a robust form, a rounded head, large rounded or oval ears, and a short, broad muzzle. Their long and naked scaly tail is typical of practically all rats and mice. Bandicoots erect their piles of long hairs and grunt when excited. Bandicoots are found practically on the whole of the subcontinent from the Himalayas to Cape Comorin, including Sri Lanka, but they are not found in the deserts and the semi-arid zones of north-west India. Here, they are replaced by a related species, the short-tailed bandicoot (see section 3.1.2 below). The bandicoot is essentially parasitic on man, living in or about human dwellings. They cause a lot of damage to grounds and fl oorings because of their burrowing habits; they also dig tunnels through bricks and masonry. -
Fleas, Hosts and Habitat: What Can We Predict About the Spread of Vector-Borne Zoonotic Diseases?
2010 Fleas, Hosts and Habitat: What can we predict about the spread of vector-borne zoonotic diseases? Ph.D. Dissertation Megan M. Friggens School of Forestry I I I \, l " FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? by Megan M. Friggens A Dissertation Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Forest Science Northern Arizona University May 2010 ?Jii@~-~-u-_- Robert R. Parmenter, Ph. D. ~",l(*~ l.~ Paulette L. Ford, Ph. D. --=z:r-J'l1jU~ David M. Wagner, Ph. D. ABSTRACT FLEAS, HOSTS AND HABITAT: WHAT CAN WE PREDICT ABOUT THE SPREAD OF VECTOR-BORNE ZOONOTIC DISEASES? MEGAN M. FRIGGENS Vector-borne diseases of humans and wildlife are experiencing resurgence across the globe. I examine the dynamics of flea borne diseases through a comparative analysis of flea literature and analyses of field data collected from three sites in New Mexico: The Sevilleta National Wildlife Refuge, the Sandia Mountains and the Valles Caldera National Preserve (VCNP). My objectives were to use these analyses to better predict and manage for the spread of diseases such as plague (Yersinia pestis). To assess the impact of anthropogenic disturbance on flea communities, I compiled and analyzed data from 63 published empirical studies. Anthropogenic disturbance is associated with conditions conducive to increased transmission of flea-borne diseases. Most measures of flea infestation increased with increasing disturbance or peaked at intermediate levels of disturbance. Future trends of habitat and climate change will probably favor the spread of flea-borne disease. -
Original Papers Ectoparasites of the Nile Rat, Arvicanthis Niloticus From
Annals of Parasitology 2019, 65(4), 411–416 Copyright© 2019 Polish Parasitological Society doi: 10.17420/ap6504.228 Original papers Ectoparasites of the Nile Rat, Arvicanthis niloticus from Shendi area, Sudan Yassir Sulieman 1, Randa E. El-Tayeb 1, Natchadaporn Srimek 2, Theerakamol Pengsakul 3 1Department of Zoology, Faculty of Science and Technology, University of Shendi, Shendi, Sudan 2Department of Biology, Faculty of Science, Prince of Songkla University, Songkhla, Thailand 3Faculty of Medical Technology, Prince of Songkla University, Hat Yai, Songkhla, Thailand Corresponding Author: Yassir Sulieman; e-mail: [email protected] ABSTRACT. This study investigated the ectoparasites of the Nile Rat, Arvicanthis niloticus in Shendi area, River Nile State, Sudan. Eighty nine A. niloticus were collected for the first time from the horticultural fields of Shendi, between January to June 2018, and their entire fur was combed thoroughly, using a fine-tooth comb. Any removed ectoparasites were relaxed, mounted and examined under a microscope for morphological identification. Forty two (47.2%) of the collected rats was found infested, with an overall mean intensity of 13.4 (range 2–67) ectoparasites per an infested rat; 10 different species of ectoparasites were identified, including: 2 species of flea – Xenopsylla cheopis , Leptopsylla segnis ; 3 species of louse – Polyplax spinulosa , P. abyssinica , P. serrata ; a species of tick – Rhipicephalus sp.; 4 species of mite – Laelaps agilis , L. nuttalli , Ornitonyssus bacoti , Dermanyssuss gallinae . The most prevalent ectoparasite found was the flea Xenopsylla cheopis , 23.6%, followed by the mite Laelaps nuttalli , 10.1%, while the least was the mite Ornitonyssus bacoti , 1.1%. Significantly higher prevalence and intensity of infestation was found among male rats. -
Endemism and Diversity of Small Mammals Along Two Neighboring Bornean Mountains
Endemism and diversity of small mammals along two neighboring Bornean mountains Miguel Camacho-Sanchez1,2,*, Melissa T.R. Hawkins3,4,5,*, Fred Tuh Yit Yu6, Jesus E. Maldonado3 and Jennifer A. Leonard1 1 Conservation and Evolutionary Genetics Group, Doñana Biological Station (EBD-CSIC), Sevilla, Spain 2 CiBIO—Centro de Investigação em Biodiversidade e Recursos Genéticos da Universidade do Porto, Vairão, Portugal 3 Center for Conservation Genomics, Smithsonian Conservation Biology Institute, National Zoological Park, Washington, DC, USA 4 Department of Biological Sciences, Humboldt State University, Arcata, CA, USA 5 Division of Mammals, National Museum of Natural History, Washington, DC, USA 6 Sabah Parks, Kota Kinabalu, Sabah, Malaysia * These authors contributed equally to this work. ABSTRACT Mountains offer replicated units with large biotic and abiotic gradients in a reduced spatial scale. This transforms them into well-suited scenarios to evaluate biogeographic theories. Mountain biogeography is a hot topic of research and many theories have been proposed to describe the changes in biodiversity with elevation. Geometric constraints, which predict the highest diversity to occur in mid-elevations, have been a focal part of this discussion. Despite this, there is no general theory to explain these patterns, probably because of the interaction among different predictors with the local effects of historical factors. We characterize the diversity of small non-volant mammals across the elevational gradient on Mount (Mt.) Kinabalu (4,095 m) and Mt. Tambuyukon (2,579 m), two neighboring mountains in Borneo, Malaysia. We documented a decrease in species richness with elevation which deviates from expectations of the geometric constraints and suggests that spatial Submitted 14 February 2018 Accepted 9 September 2019 factors (e.g., larger diversity in larger areas) are important. -
Quaternary Murid Rodents of Timor Part I: New Material of Coryphomys Buehleri Schaub, 1937, and Description of a Second Species of the Genus
QUATERNARY MURID RODENTS OF TIMOR PART I: NEW MATERIAL OF CORYPHOMYS BUEHLERI SCHAUB, 1937, AND DESCRIPTION OF A SECOND SPECIES OF THE GENUS K. P. APLIN Australian National Wildlife Collection, CSIRO Division of Sustainable Ecosystems, Canberra and Division of Vertebrate Zoology (Mammalogy) American Museum of Natural History ([email protected]) K. M. HELGEN Department of Vertebrate Zoology National Museum of Natural History Smithsonian Institution, Washington and Division of Vertebrate Zoology (Mammalogy) American Museum of Natural History ([email protected]) BULLETIN OF THE AMERICAN MUSEUM OF NATURAL HISTORY Number 341, 80 pp., 21 figures, 4 tables Issued July 21, 2010 Copyright E American Museum of Natural History 2010 ISSN 0003-0090 CONTENTS Abstract.......................................................... 3 Introduction . ...................................................... 3 The environmental context ........................................... 5 Materialsandmethods.............................................. 7 Systematics....................................................... 11 Coryphomys Schaub, 1937 ........................................... 11 Coryphomys buehleri Schaub, 1937 . ................................... 12 Extended description of Coryphomys buehleri............................ 12 Coryphomys musseri, sp.nov.......................................... 25 Description.................................................... 26 Coryphomys, sp.indet.............................................. 34 Discussion . .................................................... -
Report on Biodiversity and Tropical Forests in Indonesia
Report on Biodiversity and Tropical Forests in Indonesia Submitted in accordance with Foreign Assistance Act Sections 118/119 February 20, 2004 Prepared for USAID/Indonesia Jl. Medan Merdeka Selatan No. 3-5 Jakarta 10110 Indonesia Prepared by Steve Rhee, M.E.Sc. Darrell Kitchener, Ph.D. Tim Brown, Ph.D. Reed Merrill, M.Sc. Russ Dilts, Ph.D. Stacey Tighe, Ph.D. Table of Contents Table of Contents............................................................................................................................. i List of Tables .................................................................................................................................. v List of Figures............................................................................................................................... vii Acronyms....................................................................................................................................... ix Executive Summary.................................................................................................................... xvii 1. Introduction............................................................................................................................1- 1 2. Legislative and Institutional Structure Affecting Biological Resources...............................2 - 1 2.1 Government of Indonesia................................................................................................2 - 2 2.1.1 Legislative Basis for Protection and Management of Biodiversity and -
Life History Account for Black
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group BLACK RAT Rattus rattus Family: MURIDAE Order: RODENTIA Class: MAMMALIA M140 Written by: P. Brylski Reviewed by: H. Shellhammer Edited by: R. Duke DISTRIBUTION, ABUNDANCE, AND SEASONALITY The black rat was introduced to North America in the 1800's. Its distribution in California is poorly known, but it probably occurs in most urban areas. There are 2 subspecies present in California, R. r. rattus and R. r. alexandrinus. R. r. rattus, commonly called the black rat, lives in seaports and adjacent towns. It is frequently found along streamcourses away from buildings (Ingles 1947). R. r. alexandrinus, more commonly known as the roof rat, lives along the coast, in the interior valleys and in the lower parts of the Sierra Nevada. The distribution of both subspecies in rural areas is patchy. Occurs throughout the Central Valley and west to the San Francisco Bay area, coastal southern California, in Bakersfield (Kern Co.), and in the North Coast area from the vicinity of Eureka to the Oregon border. Confirmed locality information is lacking. Found in buildings, preferring attics, rafters, walls, and enclosed spaces (Godin 1977), and along streamcourses (Ingles 1965). Common in urban habitats. May occur in valley foothill riparian habitat at lower elevations. In northern California, occurs in dense himalayaberry thickets (Dutson 1973). SPECIFIC HABITAT REQUIREMENTS Feeding: Omnivorous, eating fruits, grains, small terrestrial vertebrates, fish, invertebrates, and human garbage. Cover: Prefers buildings and nearby stream courses. Where the black rat occurs with the Norway rat, it usually is forced to occupy the upper parts of buildings (Godin 1977). -
Habitat-Specific Shaping of Proliferation and Neuronal Differentiation in Adult Hippocampal Neurogenesis of Wild Rodents
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2013 Habitat-specific shaping of proliferation and neuronal differentiation in adult hippocampal neurogenesis of wild rodents Cavegn, Nicole ; van Dijk, R Maarten ; Menges, Dominik ; Brettschneider, Helene ; Phalanndwa, Mashudu ; Chimimba, Christian T ; Isler, Karin ; Lipp, Hans-Peter ; Slomianka, Lutz ; Amrein, Irmgard DOI: https://doi.org/10.3389/fnins.2013.00059 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-89370 Journal Article Published Version The following work is licensed under a Creative Commons: Attribution 3.0 Unported (CC BY 3.0) License. Originally published at: Cavegn, Nicole; van Dijk, R Maarten; Menges, Dominik; Brettschneider, Helene; Phalanndwa, Mashudu; Chimimba, Christian T; Isler, Karin; Lipp, Hans-Peter; Slomianka, Lutz; Amrein, Irmgard (2013). Habitat-specific shaping of proliferation and neuronal differentiation in adult hippocampal neurogenesis of wild rodents. Frontiers in Neuroscience:7:59. DOI: https://doi.org/10.3389/fnins.2013.00059 ORIGINAL RESEARCH ARTICLE published: 18 April 2013 doi: 10.3389/fnins.2013.00059 Habitat-specific shaping of proliferation and neuronal differentiation in adult hippocampal neurogenesis of wild rodents Nicole Cavegn 1, R. Maarten van Dijk 1, Dominik Menges 1, Helene Brettschneider 2,3, Mashudu Phalanndwa 2,4, Christian T. Chimimba2,5 , Karin Isler6 , Hans-Peter Lipp 1 , Lutz Slomianka1 and Irmgard -
Table 7: Species Changing IUCN Red List Status (2018-2019)
IUCN Red List version 2019-3: Table 7 Last Updated: 10 December 2019 Table 7: Species changing IUCN Red List Status (2018-2019) Published listings of a species' status may change for a variety of reasons (genuine improvement or deterioration in status; new information being available that was not known at the time of the previous assessment; taxonomic changes; corrections to mistakes made in previous assessments, etc. To help Red List users interpret the changes between the Red List updates, a summary of species that have changed category between 2018 (IUCN Red List version 2018-2) and 2019 (IUCN Red List version 2019-3) and the reasons for these changes is provided in the table below. IUCN Red List Categories: EX - Extinct, EW - Extinct in the Wild, CR - Critically Endangered [CR(PE) - Critically Endangered (Possibly Extinct), CR(PEW) - Critically Endangered (Possibly Extinct in the Wild)], EN - Endangered, VU - Vulnerable, LR/cd - Lower Risk/conservation dependent, NT - Near Threatened (includes LR/nt - Lower Risk/near threatened), DD - Data Deficient, LC - Least Concern (includes LR/lc - Lower Risk, least concern). Reasons for change: G - Genuine status change (genuine improvement or deterioration in the species' status); N - Non-genuine status change (i.e., status changes due to new information, improved knowledge of the criteria, incorrect data used previously, taxonomic revision, etc.); E - Previous listing was an Error. IUCN Red List IUCN Red Reason for Red List Scientific name Common name (2018) List (2019) change version Category -
A NEW RAT from ABYSSINIA. by Dr
A NEW RAT FROM ABYSSINIA. By Dr. Augusto Toschi. Professor in the Bologna University. NEANTHOMYS, gen novo TYPE : N eanthomys giaquintoi. A Rat (Murinae) distinguished by its rather slender, not very thick skull with nasals narrow and long, supraorbital region of skull normal, crests very slightly marked, brain-case medium, anteorbital width reduced, orbital plate about half the height of the muzzle and with anterior border not concave, incisive foramina long reaching the tooth-row, bullae rather large. Ungrooved incisors lightly pro• odont showing a subapical notch, teeth-row short, teeth generally small and reduced especially third molar. First molar longer than broad, second molar about as broad as long: M1 longer than M2 + M3, anterior lamina of M1 not reduced. Limbs and hind feet very short. Tail short (shorter than body without head). Fur thick, but not very harsh or bristly, not showing any body stripe in the known species. Neanthomys shares with the Aethomys Group the character of the 5th digit of the anterior feet reaching the base of the 4th and the 5th digit of the hind feet longer than the great toe. Neanthomys differs; from Zelotomys Osgood (the genus of the Aethomys group showing pro-odont incisors) by its shorter tail, its less soft fur, its skull without considerable interorbital constriction, its cheek-teeth not so strongly cuspidate and broad, its narrower nasals and lower orbital plate; from Dasymys Peters, StenocePhalemys Frick, Oenomys Thomas, Rattus Fischer, Aethomys Thomas, Mastomys Thomas, Praomys Thomas, Sylvaenus -
Northern Cape Provincial Gazette Vol 15 No
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