Vertebrates of Public Health Importance in California
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Mammals of the California Desert
MAMMALS OF THE CALIFORNIA DESERT William F. Laudenslayer, Jr. Karen Boyer Buckingham Theodore A. Rado INTRODUCTION I ,+! The desert lands of southern California (Figure 1) support a rich variety of wildlife, of which mammals comprise an important element. Of the 19 living orders of mammals known in the world i- *- loday, nine are represented in the California desert15. Ninety-seven mammal species are known to t ':i he in this area. The southwestern United States has a larger number of mammal subspecies than my other continental area of comparable size (Hall 1981). This high degree of subspeciation, which f I;, ; leads to the development of new species, seems to be due to the great variation in topography, , , elevation, temperature, soils, and isolation caused by natural barriers. The order Rodentia may be k., 2:' , considered the most successful of the mammalian taxa in the desert; it is represented by 48 species Lc - occupying a wide variety of habitats. Bats comprise the second largest contingent of species. Of the 97 mammal species, 48 are found throughout the desert; the remaining 49 occur peripherally, with many restricted to the bordering mountain ranges or the Colorado River Valley. Four of the 97 I ?$ are non-native, having been introduced into the California desert. These are the Virginia opossum, ' >% Rocky Mountain mule deer, horse, and burro. Table 1 lists the desert mammals and their range 1 ;>?-axurrence as well as their current status of endangerment as determined by the U.S. fish and $' Wildlife Service (USWS 1989, 1990) and the California Department of Fish and Game (Calif. -
Schall and Dearing.Pdf
Oecologia (Berlin) (1987) 73:389-392 LxA70u c Springer-Verlag 1987 Malarial parasitism and male competition for mates in the western fence lizard, Sceloporus occidentalis J.J. Schall and M.D. Dearing Department of Zoology, University of Vermont, Burlington, VT 05405, USA Summary. The effect of malarial parasitism on the ability the outcome of male-male interactions and female choice of male western fence lizards, Sceloporus occidentalis, to in the western fence lizard, Sceloporusoccidentalis, in Cali- compete for access to females was assessed experimentally. fornia, USA. The mating system of S. occidentalisis polyga- Pairs of male lizards, one infected with the malarial para- mous. Males interact agonistically toward other males and site, Plasmodium mexicanum, and the other not infected, vigorously court females during the reproductive season. were matched by size and color and placed in large semina- Their conspicuous stereotyped behaviors include bobbing, tural outdoor enclosures along with an adult female lizard. shaking, and display of brightly colored ventral color Infected males displayed to females and to other males less patches (Schall and Sarni 1987; Ressel 1986). At our study often than did noninfected male lizards. Noninfected lizards site approximately 25% of adult male fence lizards are in- were dominant in social interactionsmore often than malar- fected with the malarial parasite, Plasmodiummexicanum ious animals, based on duration and intensity of agonistic (Schall 1983; Bromwich and Schall 1986). This parasite re- encounters toward the other male, and time spent with the duces the ability of the fence lizard to engage in intense female. Thus, malarial infection hinders the ability of male activity; infected males also have smaller testes (Schall fence lizards to compete for mates. -
Mammal Pests
VERTEBRATE PEST CONT ROL HANDBOOK - MAMMALS Mammal Pests Introduction This section contains methods used to control field rodents and rabbits and is a guide for agricultural commissioner personnel engaged in this work. Most pest mammals are discussed with specific control options. Rodenticides are often recommended. Before rodenticides are used, acceptance tests should be made to indicate the degree of bait acceptance that can be expected. If bait acceptance is good, most of the bait will be quickly consumed by rodents during a 24-hour period. If acceptance is poor, toxic bait should not be used. Too frequent application of acute toxic baits, like zinc phosphide, may cause bait and poison shyness. Unlike insecticides, which are generally applied to the crop itself, rodent baits are commonly placed in rodent burrows or applied to trails or areas where rodents naturally feed. Rodent baits should not be applied in any manner that will contaminate food or feed crops. This would include any application method which would cause the bait to lodge in food plants. Fumigants are applied directly into the rodent burrow and are sealed in by covering the burrow opening with a shovelful of dirt. Identifying Rodents Causing Damage to Crops One of the keys to controlling rodent damage in crops is prompt and accurate determination of which species is causing the damage. To make a positive species identification, survey the area of reported damage and look for signs of rodent activity such as: trails, runs, tracks and tail marks, droppings, burrows, nests and food caches. Also look for cuttings of grass or plant material in trails, runs or near burrow entrances. -
Hispid Pocket Mouse Chaetodipus Hispidus
Wyoming Species Account Hispid Pocket Mouse Chaetodipus hispidus REGULATORY STATUS USFWS: No special status USFS R2: No special status USFS R4: No special status Wyoming BLM: No special status State of Wyoming: Nongame Wildlife CONSERVATION RANKS USFWS: No special status WGFD: NSSU (U), Tier III WYNDD: G5, S1S3 Wyoming Contribution: LOW IUCN: Least Concern STATUS AND RANK COMMENTS The Wyoming Natural Diversity Database has assigned Hispid Pocket Mouse (Chaetodipus hispidus) a state conservation rank ranging from S1 (Critically Imperiled) to S3 (Vulnerable) because of uncertainty about the proportion of range occupied and population trends for this species in Wyoming. NATURAL HISTORY Taxonomy: Historically, there were four recognized subspecies of Hispid Pocket Mouse, and only C. h. paradoxus was found in Wyoming 1-5. A recent DNA-based study determined that the previously accepted subspecies are neither morphologically nor genetically distinct and instead proposed new subspecies boundaries delineated by four geographically and ecologically disjunct mitochondrial clades 6. Following this taxonomic revision, Wyoming remains within the distribution of the newly defined subspecies C. h. paradoxus 6. Description: It is possible to identify Hispid Pocket Mouse in the field. It is the largest Wyoming pocket mouse species; adults weigh between 40–60 g and can reach total lengths of 200–223 mm 2. Tail, hind foot, and ear length ranges from 90–113 mm, 25–28 mm, and 12–13 mm, respectively 2. Hispid Pocket Mouse is named for its distinctly coarse dorsal pelage, which is buff to yellowish orange mixed with black hairs, thus leading to an overall brownish or even olive appearance 1, 2, 4, 5, 7. -
USGS DDS-43, Status of Terrestrial Vertebrates
DAVID M. GRABER National Biological Service Sequoia and Kings Canyon Field Station Three Rivers, California 25 Status of Terrestrial Vertebrates ABSTRACT The terrestrial vertebrate wildlife of the Sierra Nevada is represented INTRODUCTION by about 401 regularly occurring species, including three local extir- There are approximately 401 species of terrestrial vertebrates pations in the 20th century. The mountain range includes about two- that use the Sierra Nevada now or in recent times according thirds of the bird and mammal species and about half the reptiles to the California Wildlife Habitat Relationships System and amphibians in the State of California. This is principally because (CWHR) (California Department of Fish and Game 1994) (ap- of its great extent, and because its foothill woodlands and chaparral, pendix 25.1). Of these, thirteen are essentially restricted to mid-elevation forests, and alpine vegetation reflect, in structure and the Sierra in California (one of these is an alien; i.e. not native function if not species, habitats found elsewhere in the State. About to the Sierra Nevada); 278 (eight aliens) include the Sierra in 17% of the Sierran vertebrate species are considered at risk by state their principal range; and another 110 (six aliens) use the Si- or federal agencies; this figure is only slightly more than half the spe- erra as a minor portion of their range. Included in the 401 are cies at risk for the state as a whole. This relative security is a function 232 species of birds; 112 species of mammals; thirty-two spe- of the smaller proportion of Sierran habitats that have been exten- cies of reptiles; and twenty-five species of amphibians (ap- sively modified. -
ALTRUISM, RISK, ENERGY DEVELOPMENT and the HUMAN-ANIMAL RELATIONSHIP by Cameron Thomas Whitley a DISSERTATION Submitted to Michi
ALTRUISM, RISK, ENERGY DEVELOPMENT AND THE HUMAN-ANIMAL RELATIONSHIP By Cameron Thomas Whitley A DISSERTATION Submitted to Michigan State University in partial fulfillment of the requirements for the degree of Sociology – Doctor of Philosophy 2017 ABSTRACT ALTRUISM, RISK, ENERGY DEVELOPMENT AND THE HUMAN-ANIMAL RELATIONSHIP By Cameron Thomas Whitley Research shows that humans form relationships with animals that alter social, psychological and biological processes. However, within environmental decision-making and social psychological research, the importance of human-animal relationships has not been thoroughly explored. This dissertation extends social distance theories to include human-animal relationships and utilizes environmental values, particularly altruism, in a causal chain to assess how individuals perceive the risk high volume horizontal drilling hydraulic fracturing (HVHHF) poses to animals. HVHHF is an ideal lens to investigate this topic because this technology puts animals at substantial risk of harm and creates environments that simultaneously affect humans and animals. In Chapter 1 I conduct a thorough content analysis of peer-reviewed HVHHF articles to examine how animals and human-animal relationships are represented. The analysis demonstrates that existing research seldom acknowledges animals’ inherent value, instead focusing almost exclusively on the use of animals as sentinels for potential human health risks. Furthermore, there are no social science articles assessing the impacts of HVHHF on animals or human-animal relationships. This chapter serves as a call for additional research. I use Chapters 2 and 3 to respond to this call, exploring the social and psychological drivers of perceptions of the risk HVHHF poses to humans and animals. In Chapter 2 I use an experimental survey design to extend construal level theory of psychological distance (CLT) to interspecies relationships and test whether social distance between species influences human perceptions of HVHHF risk to animals. -
Colorado Field Ornithologists the Colorado Field Ornithologists' Quarterly
Journal of the Colorado Field Ornithologists The Colorado Field Ornithologists' Quarterly VOL. 36, NO. 1 Journal of the Colorado Field Ornithologists January 2002 Vol. 36, No. 1 Journal of the Colorado Field Ornithologists January 2002 TABLE OF C ONTENTS A LETTER FROM THE E DITOR..............................................................................................2 2002 CONVENTION IN DURANGO WITH KENN KAUFMANN...................................................3 CFO BOARD MEETING MINUTES: 1 DECEMBER 2001........................................................4 TREE-NESTING HABITAT OF PURPLE MARTINS IN COLORADO.................................................6 Richard T. Reynolds, David P. Kane, and Deborah M. Finch OLIN SEWALL PETTINGILL, JR.: AN APPRECIATION...........................................................14 Paul Baicich MAMMALS IN GREAT HORNED OWL PELLETS FROM BOULDER COUNTY, COLORADO............16 Rebecca E. Marvil and Alexander Cruz UPCOMING CFO FIELD TRIPS.........................................................................................23 THE SHRIKES OF DEARING ROAD, EL PASO COUNTY, COLORADO 1993-2001....................24 Susan H. Craig RING-BILLED GULLS FEEDING ON RUSSIAN-OLIVE FRUIT...................................................32 Nicholas Komar NEWS FROM THE C OLORADO BIRD R ECORDS COMMITTEE (JANUARY 2002).........................35 Tony Leukering NEWS FROM THE FIELD: THE SUMMER 2001 REPORT (JUNE - JULY)...................................36 Christopher L. Wood and Lawrence S. Semo COLORADO F IELD O -
A Newly Identified Hantavirus: the Development of Immunologic Diagnostic Assays and Phylogenetic Analysis for Detection and Characterization
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-2005 A Newly Identified Hantavirus: The Development of Immunologic Diagnostic Assays and Phylogenetic Analysis for Detection and Characterization Shawn Lee Lewis University of Tennessee, Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Medicine and Health Sciences Commons Recommended Citation Lewis, Shawn Lee, "A Newly Identified Hantavirus: The Development of Immunologic Diagnostic Assays and Phylogenetic Analysis for Detection and Characterization. " PhD diss., University of Tennessee, 2005. https://trace.tennessee.edu/utk_graddiss/4368 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Shawn Lee Lewis entitled "A Newly Identified Hantavirus: The Development of Immunologic Diagnostic Assays and Phylogenetic Analysis for Detection and Characterization." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Comparative and Experimental Medicine. John -
Ventral Coloration and Body Condition Do Not Affect Territorial Behavior in Two Sceloporus Lizards
Ventral coloration and body condition do not affect territorial behavior in two Sceloporus lizards 1Marina Kelada, 1Courtney Moulton, 2Casey Nguyen, 3Griselda Robles Olague 1University of California, Riverside; 2University of California, Irvine; 3University of California, Santa Barbara Sceloporus lizards are known to be defensive of their territories, which provide shelter, food, water, and mates. They often exhibit territorial behavior through visual displays of aggression, specifically with pushups. Along with aggression, this display can also expose the blue coloration on their ventral side, serving as an intraspecific communication between lizards that reveals information about their dominance, sex, and species membership. In this study, we compared how blue coloration and body condition affected territorial behavior in two Sceloporus lizards: the well-studied western fence (Sceloporus occidentalis) and the understudied sagebrush (Sceloporus graciosus), two closely related lizards with overlapping ranges in the San Jacinto Mountains. We also addressed whether these species would exhibit character displacement in their ventral coloration as a result of their sympatry. ImageJ and Adobe Photoshop were used for photo analyses to quantify the proportion and intensity of blue on each lizard’s ventral side. Territoriality was measured through number of pushups displayed and distance traveled. We found that both ventral coloration and body condition had no effect on the territoriality of either species, suggesting that territorial behavior -
Life History Account for Panamint Chipmunk
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group PANAMINT CHIPMUNK Tamias panamintinus Family: SCIURIDAE Order: RODENTIA Class: MAMMALIA M064 Written by: J. Harris Reviewed by: H. Shellhammer Edited by: R. Duke DISTRIBUTION, ABUNDANCE, AND SEASONALITY The Panamint chipmunk occurs along the eastside of the southern Sierra Nevada, and in the desert ranges of southern Mono Co. south to San Bernardino Co. It is a common, yearlong resident of pinyon-juniper and juniper habitats, residing primarily in rocky outcrops in these habitats. Ranges from 1700-2700 m (5700-9000 ft) SPECIFIC HABITAT REQUIREMENTS Feeding: Primarily granivorous, but reported foods include pinyon and juniper fruits (Burt 1934), willow catkins (Hall 1946), seeds, fruits, green vegetation, arthropods, some lichens, bark, and carrion. Captive animals consumed 4-5.5 g of food per day (Hirshfeld 1975). Forages on ground, in shrubs, and trees. Probably caches. Cover: Uses rocks and ground burrows for shelter and nesting. Probably uses the shade of trees and rocks for thermoregulation. Reproduction: Uses rocks and ground burrows for nesting. Water: Does not require a source of water other than food, but will use water if available. Pattern: Primarily a rock dweller. Soil is thin in preferred habitat; fissured granite cliffs and ledges are abundant. Closely tied to presence of pinyon pine (Johnson 1940). SPECIES LIFE HISTORY Activity Patterns: Diurnal. This species is a facuItative hibernator, depending on temperature and snow cover. May also show reduced activity in hot summer months. Seasonal Movements/Migration: None reported. Home Range: No data found. Territory: Probably defends nest area. -
Biology 2 Lab Packet for Practical 4
1 Biology 2 Lab Packet For Practical 4 2 CLASSIFICATION: Domain: Eukarya Supergroup: Unikonta Clade: Opisthokonts Kingdom: Animalia Phylum: Chordata – Chordates Subphylum: Urochordata - Tunicates Class: Amphibia – Amphibians Subphylum: Cephalochordata - Lancelets Order: Urodela - Salamanders Subphylum: Vertebrata – Vertebrates Order: Apodans - Caecilians Superclass: Agnatha Order: Anurans – Frogs/Toads Order: Myxiniformes – Hagfish Class: Testudines – Turtles Order: Petromyzontiformes – Lamprey Class: Sphenodontia – Tuataras Superclass: Gnathostomata – Jawed Vertebrates Class: Squamata – Lizards/Snakes Class: Chondrichthyes - Cartilaginous Fish Lizards Subclass: Elasmobranchii – Sharks, Skates and Rays Order: Lamniiformes – Great White Sharks Family – Agamidae – Old World Lizards Order: Carcharhiniformes – Ground Sharks Family – Anguidae – Glass Lizards Order: Orectolobiniformes – Whale Sharks Family – Chameleonidae – Chameleons Order: Rajiiformes – Skates Family – Corytophanidae – Helmet Lizards Order: Myliobatiformes - Rays Family - Crotaphytidae – Collared Lizards Subclass: Holocephali – Ratfish Family – Helodermatidae – Gila monster Order: Chimaeriformes - Chimaeras Family – Iguanidae – Iguanids Class: Sarcopterygii – Lobe-finned fish Family – Phrynosomatidae – NA Spiny Lizards Subclass: Actinistia - Coelocanths Family – Polychrotidae – Anoles Subclass: Dipnoi – Lungfish Family – Geckonidae – Geckos Class: Actinopterygii – Ray-finned Fish Family – Scincidae – Skinks Order: Acipenseriformes – Sturgeon, Paddlefish Family – Anniellidae -
1 CWU Comparative Osteology Collection, List of Specimens
CWU Comparative Osteology Collection, List of Specimens List updated November 2019 0-CWU-Collection-List.docx Specimens collected primarily from North American mid-continent and coastal Alaska for zooarchaeological research and teaching purposes. Curated at the Zooarchaeology Laboratory, Department of Anthropology, Central Washington University, under the direction of Dr. Pat Lubinski, [email protected]. Facility is located in Dean Hall Room 222 at CWU’s campus in Ellensburg, Washington. Numbers on right margin provide a count of complete or near-complete specimens in the collection. Specimens on loan from other institutions are not listed. There may also be a listing of mount (commercially mounted articulated skeletons), part (partial skeletons), skull (skulls), or * (in freezer but not yet processed). Vertebrate specimens in taxonomic order, then invertebrates. Taxonomy follows the Integrated Taxonomic Information System online (www.itis.gov) as of June 2016 unless otherwise noted. VERTEBRATES: Phylum Chordata, Class Petromyzontida (lampreys) Order Petromyzontiformes Family Petromyzontidae: Pacific lamprey ............................................................. Entosphenus tridentatus.................................... 1 Phylum Chordata, Class Chondrichthyes (cartilaginous fishes) unidentified shark teeth ........................................................ ........................................................................... 3 Order Squaliformes Family Squalidae Spiny dogfish ........................................................