Mammals of Scotts Bluff
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The Dispersal and Acclimatization of the Muskrat, Ondatra Zibethicus (L.), in Finland
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Wildlife Damage Management, Internet Center Other Publications in Wildlife Management for 1960 The dispersal and acclimatization of the muskrat, Ondatra zibethicus (L.), in Finland Atso Artimo Suomen Riistanhoito-Saatio (Finnish Game Foundation) Follow this and additional works at: https://digitalcommons.unl.edu/icwdmother Part of the Environmental Sciences Commons Artimo, Atso, "The dispersal and acclimatization of the muskrat, Ondatra zibethicus (L.), in Finland" (1960). Other Publications in Wildlife Management. 65. https://digitalcommons.unl.edu/icwdmother/65 This Article is brought to you for free and open access by the Wildlife Damage Management, Internet Center for at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Other Publications in Wildlife Management by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. R I 1ST A TIE T L .~1 U ( K A I S U J A ,>""'liSt I " e'e 'I >~ ~··21' \. • ; I .. '. .' . .,~., . <)/ ." , ., Thedi$perscdQnd.a~C:li"'dti~otlin. of ,the , , :n~skret, Ond~trq ~ib.t~i~',{(.h in. Firtland , 8y: ATSO ARTIMO . RllSTATIETEELLISljX JULKAISUJA PAPERS ON GAME RESEARCH 21 The dispersal and acclimatization of the muskrat, Ondatra zibethicus (l.), in Finland By ATSO ARTIMO Helsinki 1960 SUOMEN FIN LANDS R I 1ST A N HOI T O-S A A T I b ] AK TV ARDSSTI FTELSE Riistantutkimuslaitos Viltforskningsinstitutet Helsinki, Unionink. 45 B Helsingfors, Unionsg. 45 B FINNISH GAME FOUNDATION Game Research Institute Helsinki, Unionink. 45 B Helsinki 1960 . K. F. Puromichen Kirjapaino O.-Y. The dispersal and acclimatization of the muskrat, Ondatra zibethicus (L.), in Finland By Atso Artimo CONTENTS I. -
Emory Health
Health care for the working poor 8 After cancer, what next? 12 Smallpox chronicles 25 PATIENT CARE, RESEARCH, AND EDUCATION FROM Spring 2010 THE WOODRUFF HEALTH SCIENCES CENTER Why do voles fall in love? And what that means for human health. 2 FEATURE LISTENING TO THE HORMONES CouplingBy Sylvia Wrobel Monogamy—vole style What does love—or at least monogamy—have to do with autism, schizophrenia, and other conditions with deficits in socialcial awarenessawareness and attachment? Larry Young (left) believes his quirky little prairie voles hold some answers. Once mating is over, fidelity does not come naturally to the vast majority of species.. Even within species whose members do engage in social bonding, like humans, some individuals are better at it than others. The popular question was, “Why do voles fall In the 1990s, Young (William P. Timmie in love?” The answer, said the scientists, was that oxytocin created lifelong attachment. Professor of Psychiatry at Emory and chief of behavioral neuroscience at Yerkes National Primate Research Center) and Tom Insel (then director of Yerkes and now director of the National Institute of Mental Health) created a scientific and media storm when they reported that the surprisingly ubiquitous and long-lasting monogamy exhibited by a species of voles is attributable to hormones. The popular ques- tion was, “Why do voles fall in love?” The answer, said the scientists, was that oxytocin—the same hormone released during labor, delivery, and breast feeding in humans and that promotes mother-infant bonding— creates the female prairie vole’s lifelong attachment to her male partner. -
Microtus Ochrogaster) from the Southern Plains of Texas and Oklahoma
OCCASIONAL PAPERS Museum of Texas Tech University Number 235 5 May 2004 HISTORICAL ZOOGEOGRAPHY AND TAXONOMIC STATUS OF THE PRAIRIE VOLE (MICROTUS OCHROGASTER) FROM THE SOUTHERN PLAINS OF TEXAS AND OKLAHOMA FREDERICK B. STANGL, JR., JIM R. GOETZE, AND KIMBERLY D. SPRADLING The prairie vole (Microtus ochrogaster) today is with distinct cranial characters andpale pelage colora considered a species ofthe Great Plains, whose range tion, they described M. o. taylori. extends from the interior grasslands ofsouthern Canada to central Oklahoma and the northernTexas Panhandle, Choate and Williams (1978) perfonned a mor and is generally bordered by the Rocky Mountains to phometric analysis ofthe prairie vole, which included the west and the eastern deciduous woodlands (Bee et material reported onby Hibbard and Rinker (1943) as al. 1981; Hall 1981; Hoffmann andKoeppl 1985; Caire M. o. taylori. Each of their external body measure et al. 1990; Stalling 1990). Duringthe late Pleistocene, ments and four of the seven cranial characters (skull the species occurred throughout much ofTexas, leav length, zygomatic breadth, mastoidal breadth, and least ing fossil evidence as far south as the Edwards Pla interorbital breadth) exhibited significant geographic teau and parts ofthe GulfCoast (Dalquest and Schultz variation. While no geographic patterns were evident 1992; Graham 1987). The species retreated north to suggest subspecific levels of differentiation, popu ward with the advent ofincreasingly arid climate dur lations from the Dakotas to Kansas demonstrated a ing the Holocene. At least one isolated population, M. slight north-to-south elinal increase in size of cranial o. ludovicianus, was stranded during this time, and is characters. -
Young, L.J., & Hammock E.A.D. (2007)
Update TRENDS in Genetics Vol.23 No.5 Research Focus On switches and knobs, microsatellites and monogamy Larry J. Young1 and Elizabeth A.D. Hammock2 1 Department of Psychiatry and Behavioral Sciences, Center for Behavioral Neuroscience, 954 Gatewood Road, Yerkes National Primate Research Center, Emory University School of Medicine, Atlanta, GA 30322, USA 2 Vanderbilt Kennedy Center and Department of Pharmacology, 465 21st Avenue South, MRBIII, Room 8114, Vanderbilt University, Nashville, TN 37232, USA Comparative studies in voles have suggested that a formation. In male prairie voles, infusion of vasopressin polymorphic microsatellite upstream of the Avpr1a locus facilitates the formation of partner preferences in the contributes to the evolution of monogamy. A recent study absence of mating [7]. The distribution of V1aR in the challenged this hypothesis by reporting that there is no brain differs markedly between the socially monogamous relationship between microsatellite structure and mon- and socially nonmonogamous vole species [8]. Site-specific ogamy in 21 vole species. Although the study demon- pharmacological manipulations and viral-vector-mediated strates that the microsatellite is not a universal genetic gene-transfer experiments in prairie, montane and mea- switch that determines mating strategy, the findings do dow voles suggest that the species differences in Avpr1a not preclude a substantial role for Avpr1a in regulating expression in the brain underlie the species differences in social behaviors associated with monogamy. social bonding among these three closely related species of vole [3,6,9,10]. Single genes and social behavior Microsatellites and monogamy The idea that a single gene can markedly influence Analysis of the Avpr1a loci in the four vole species complex social behaviors has recently received consider- mentioned so far (prairie, montane, meadow and pine voles) able attention [1,2]. -
Cottontail Rabbits
Cottontail Rabbits Biology of Cottontail Rabbits (Sylvilagus spp.) as Prey of Golden Eagles (Aquila chrysaetos) in the Western United States Photo Credit, Sky deLight Credit,Photo Sky Cottontail Rabbits Biology of Cottontail Rabbits (Sylvilagus spp.) as Prey of Golden Eagles (Aquila chrysaetos) in the Western United States U.S. Fish and Wildlife Service Regions 1, 2, 6, and 8 Western Golden Eagle Team Front Matter Date: November 13, 2017 Disclaimer The reports in this series have been prepared by the U.S. Fish and Wildlife Service (Service) Western Golden Eagle Team (WGET) for the purpose of proactively addressing energy-related conservation needs of golden eagles in Regions 1, 2, 6, and 8. The team was composed of Service personnel, sometimes assisted by contractors or outside cooperators. The findings and conclusions in this article are those of the authors and do not necessarily represent the views of the U.S. Fish and Wildlife Service. Suggested Citation Hansen, D.L., G. Bedrosian, and G. Beatty. 2017. Biology of cottontail rabbits (Sylvilagus spp.) as prey of golden eagles (Aquila chrysaetos) in the western United States. Unpublished report prepared by the Western Golden Eagle Team, U.S. Fish and Wildlife Service. Available online at: https://ecos.fws.gov/ServCat/Reference/Profile/87137 Acknowledgments This report was authored by Dan L. Hansen, Geoffrey Bedrosian, and Greg Beatty. The authors are grateful to the following reviewers (in alphabetical order): Katie Powell, Charles R. Preston, and Hillary White. Cottontails—i Summary Cottontail rabbits (Sylvilagus spp.; hereafter, cottontails) are among the most frequently identified prey in the diets of breeding golden eagles (Aquila chrysaetos) in the western United States (U.S.). -
Informes Individuales IUCN 2018.Indd
IUCN SSC Lagomorph Specialist Group 2018 Report Andrew Smith Hayley Lanier Co-Chairs Mission statement Targets for the 2017-2020 quadrennium Andrew Smith (1) To promote the conservation and effective Assess (2) Hayley Lanier sustainable management of all species of Red List: (1) improve knowledge and assess- lagomorph through science, education and ment of lagomorph systematics, (2) complete Red List Authority Coordinator advocacy. all Red List reassessments of all lagomorph Charlotte Johnston (1) species. Projected impact for the 2017-2020 Research activities: (1) improve knowledge of Location/Affiliation quadrennium Brachylagus idahoensis; (2) examine popula- (1) School of Life Sciences, Arizona State The Lagomorph Specialist Group (LSG) is tion trends of all lagomorphs in the western University, Tempe, Arizona, US “middle-sized” – not a single species, nor United States; (3) improve knowledge of Lepus (2) Sam Noble Museum, University of Oklahoma, composed of hundreds of species. We have callotis; (4) improve knowledge of Lepus fagani, Norman, Oklahoma, US slightly less than 100 species in our brief. L. habessinicus, and L. starcki in Ethiopia; However, these are distributed around the (5) improve knowledge of Lepus flavigularis; Number of members globe, and there are few similarities among (6) improve knowledge of all Chinese Lepus; 73 any of our many forms that are Red List clas- (7) improve knowledge of Nesolagus netscheri; sified as Threatened. Thus, we do not have a (8) improve knowledge of Nesolagus timminsi; Social networks single programme or a single thrust; there is no (9) improve knowledge of Ochotona iliensis; Website: one-size-fits-all to our approach. LSG members (10) improve surveys of poorly-studied www.lagomorphspecialistgroup.org largely work independently in their region, and Ochotona in China; (11) understand the role the Co-Chairs serve more as a nerve centre. -
Southern Bog Lemming, Synaptomys Cooperi,Andthe Mammals: Their Natural History, Classification, and Meadow Vole, Microtus Pennsylvanicus,Invirginia
Synaptomys cooperi (Baird, 1858) SBLE W. Mark Ford and Joshua Laerm CONTENT AND TAXONOMIC COMMENTS There are eight subspecies of the southern bog lem- ming (Synaptomys cooperi) recognized, four of which occur in the South: S. c. gossii, S. c. helaletes, S. c. kentucki, and S. c. stonei (Wetzel 1955, Barbour 1956, Hall 1981, Linzey 1983, Long 1987). However, Whitaker and Hamilton (1998) indicate that S. c. gossii, S. c. kentucki, and S. c. stonei could be referable to S. c. cooperi.The literature was reviewed by Linzey (1983). DISTINGUISHING CHARACTERISTICS The southern bog lemming is a robust, short-tailed vole with a broad head, small ears, and small eyes. Its measurements are: total length, 119–154 mm; tail, 13–25 mm; hind foot, 16–24 mm; ear, 8–14 mm; weight, 20–50 g. The dental formula for this species is: I 1/1, C 0/0, P 0/0, M 3/3 = 16 (Figure 1). The pel- age is bright chestnut to dark grizzled brown dor- sally, grading into silver grayish white ventrally, with gray to brown feet and tail. The southern bog lemming readily is distinguished from other voles by its short tail (usually less than hind foot length), pres- ence of a shallow longitudinal groove along upper incisors, and deep reentrant angles on molars. See keys for details. CONSERVATION STATUS The southern bog lemming has a global rank of Secure (NatureServe 2007). It is listed as Secure in Virginia and Apparently Secure in Kentucky and Tennessee. It is listed as Vulnerable in North Carolina, Imperiled in Arkansas, and Critically Imperiled in Georgia. -
Nesting Ecology of the Great Horned Owl Bubo Virginianus in Central Western Utah
Brigham Young University BYU ScholarsArchive Theses and Dissertations 1968-08-01 Nesting ecology of the great horned owl Bubo virginianus in central western Utah Dwight Glenn Smith Brigham Young University - Provo Follow this and additional works at: https://scholarsarchive.byu.edu/etd BYU ScholarsArchive Citation Smith, Dwight Glenn, "Nesting ecology of the great horned owl Bubo virginianus in central western Utah" (1968). Theses and Dissertations. 7883. https://scholarsarchive.byu.edu/etd/7883 This Thesis is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. NESTING ECOLOGYOF THE GREATHORNED OWL BUBOVIRGINIANUS IN CENTRALWESTERN UTAH L A Thesis Presented to the Department of Zoology and Entomology Brigham Young University In Partial Fulfi I lment of the Requirements for the Degree Master of Science by Dwight G. Smith August 1968 This thesis by Dwight G. Smith is accepted in its present form by the Department of Zoology and Entomolo�y of Brigham Young University as satisfying the thesis require ment for the degree of Master of Science. Typed by Beth Anne Smith f i i ACKNOWLEDGMENTS Grateful acknowledgment is made for the valuable sug- gestions and help given by the chairman of my advisory com- mittee, Dr. Joseph R. Murphy, and other members of my com- mittee, Dr. C. Lynn Hayward and Dr. Joseph R. Murdock. Ap- preciation is extended to Dr. Herbert H. Frost for his editor- ial help in the preparation of the manuscript. -
Proceedings of the Indiana Academy of Science (1988) Volume 98 P
Proceedings of the Indiana Academy of Science (1988) Volume 98 p. 553-559. BARN OWL FOOD HABITS IN INDIANA Allen R. Parker Indiana Department of Natural Resources Division of Fish & Wildlife Nongame and Endangered Wildlife Program 300 West First St. Bloomington, Indiana 47403 ABSTRACT: Pellets from barn owls {Tyto alba) were col- lected in Indiana from 1983 to 1987. Skulls, mandibles, palate fragments, and non-principal prey parts were identified and tallied. Prey biomass was estimated using weights from the literature. Of the 12,905 prey items identified, 66% of them were voles {Microtus spp. and Synaptomys cooperi). Major prey buffer species were deer mice {Peromyscus sp.) and short-tailed shrews {Blarina brevicauda). Regional examination of food habits was conducted on 16 areas, and vole dependence ranged from 31% to 80%. The meadow vole {M. pennsylvanicus) was the most important prey species in all but the southwestern coun- ties, where the prairie vole {M. ochrogaster) was most impor- tant. Seasonally, food habits varied only slightly. The mean weight per prey item was lower in Indiana than were those reported for other States. INTRODUCTION The common barn owl {Tyto alba pratincola) is on endangered species lists in 7 midwestern states (Rosenburg, 1986), and its decline has been attributed to changes in agricultural practices (Colvin, 1985). Past research in the Ohio Valley and the eastern United States has revealed that the meadow vole {Microtus penn- sylvanicus) is the primary prey of the barn owl (Colvin and McLean, 1986; Pearson and Pearson, 1947; Rosenburg, 1986). Analysis of small collections of barn owl pellets from Indiana supported this finding (Castrale, et al., 1983). -
Biology, Legal Status, Control Materials, and Directions for Use
VERTEBRATE PEST CONTROL HANDBOOK - MAMMALS BIOLOGY, LEGAL STATUS, CONTROL MATERIALS, AND DIRECTIONS FOR USE Rabbits – Black-tailed Jackrabbit, Cottontail Rabbit, Brush Rabbit Family: Leporidae Fig. 1. Black-tailed jackrabbit (Lepus californicus) Fig. 2. Desert cottontail rabbit (Sylvilagus audobonii) Fig. 3. Brush rabbit (S. bachmani) Introduction: Three rabbits are common to California: the black-tailed jackrabbit, the cottontail, and the brush rabbit. Of these, the jackrabbit is the most destructive because of its greater size and occurrence in agricultural areas. Cottontails are common pests in landscaped areas. Hereinafter ‘rabbits’ shall refer to all three species unless distinguished otherwise. Rabbits can be destructive and eat a wide variety of plants, grasses, grains, alfalfa, vegetables, fruit trees, vines, and many ornamentals. They also cause damage to plastic irrigation through their gnawing activities. Identification: The black-tailed jackrabbit (Fig. 1) is about the size of a house cat, 17 to 22 inches long. It has long ears, short front legs, and long hind legs. They populate open or semi open lands in valleys and foothills. Desert cottontail (Fig. 2) and brush rabbits (Fig. 3) are smaller (14.5 to 15.5, and 12.0 to 14.5 inches in length, respectively) and have shorter ears. Brush rabbits can be distinguished from cottontails by their smaller, inconspicuous tail and uniformly colored ears that lack a black tip. They inhabit brushy areas where cover is dense; landscaped areas provide excellent habitat. They can also be found beneath junipers and other large, low-growing evergreen shrubs. 262 VERTEBRATE PEST CONTROL HANDBOOK - MAMMALS Legal Status: Black-tailed jackrabbits, desert cottontails, and brush rabbits are classed as nongame animals in most states, but are considered game mammals by the California Fish and Game Code. -
Habitat, Home Range, Diet and Demography of the Water Vole (Arvicola Amphibious): Patch-Use in a Complex Wetland Landscape
_________________________________________________________________________Swansea University E-Theses Habitat, home range, diet and demography of the water vole (Arvicola amphibious): Patch-use in a complex wetland landscape. Neyland, Penelope Jane How to cite: _________________________________________________________________________ Neyland, Penelope Jane (2011) Habitat, home range, diet and demography of the water vole (Arvicola amphibious): Patch-use in a complex wetland landscape.. thesis, Swansea University. http://cronfa.swan.ac.uk/Record/cronfa42744 Use policy: _________________________________________________________________________ This item is brought to you by Swansea University. Any person downloading material is agreeing to abide by the terms of the repository licence: copies of full text items may be used or reproduced in any format or medium, without prior permission for personal research or study, educational or non-commercial purposes only. The copyright for any work remains with the original author unless otherwise specified. The full-text must not be sold in any format or medium without the formal permission of the copyright holder. Permission for multiple reproductions should be obtained from the original author. Authors are personally responsible for adhering to copyright and publisher restrictions when uploading content to the repository. Please link to the metadata record in the Swansea University repository, Cronfa (link given in the citation reference above.) http://www.swansea.ac.uk/library/researchsupport/ris-support/ Habitat, home range, diet and demography of the water vole(Arvicola amphibius): Patch-use in a complex wetland landscape A Thesis presented by Penelope Jane Neyland for the degree of Doctor of Philosophy Conservation Ecology Research Team (CERTS) Department of Biosciences College of Science Swansea University ProQuest Number: 10807513 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. -
SIA Border Cameras Report
Sky Island Alliance’s Border Camera Summary JUNE 28 2019 SKY ISLAND ALLIANCE by: Meagan Bethel 1 Sky Island Alliance’s Border Camera Summary This report summarizes the data collected by Sky Island Alliance’s remote sensing wildlife cameras over 23 months of sampling effort starting July 2017 and running to the most recent data of May 2019. While Sky Island Alliance maintains more than thirty cameras, 24 cameras are within 35 miles of the United States-Mexico border. Those 24 cameras along the border contributed photo data to this report. 2 Total number of photos for all border cameras by month 4000 3500 3000 2500 2000 Number of Photos 1500 1000 500 0 Figure 1 The total number of unique wildlife photos collected by Sky Island Alliance’s border cameras that spans 23 months. Two peaks can be seen in October 2017 and May 2018, however the total number of photos collected has been declining over time. 3 Table 1 A summary table of all species detected by the remote cameras with in sampling period. There were 45,886 photos with animals in them. Humans and domestic animals are separated from wildlife. Wildlife Number of Photos Humans and Number of Photos Domestic animals White-tailed deer 23994 Cattle 12001 Javelina 1915 Human hiker 1093 White-nosed coati 1159 Domestic dog 292 Mule deer 923 Vehicle 1000 Mountain lion 827 Horseback rider 90 Coyote 758 Border patrol 87 Raccoon 619 Cat 11 Turkey 398 Black Bear 366 Spotted skunk Grey fox 242 Bobcat 224 Hooded skunk 162 Desert cottontail 100 Bird species 86 Striped skunk 78 Mexican jay 68 Antelope