A Most Dangerous Game: Death and Injury to Birds from Porcupine Quills
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Spatial Relationships of Nesting Golden Eagles in Central Utah
White, C. M. 1974. The 1974 raptor surveyof the AlaskaPipeline between Franklin Bluffsand Big Delta. Unpubl.interim rep. to U.S.Fish and Wildl. Serv.,Anchorage, AK. 10 pp. White, C. M., T. D. Ray,and L. W. Sowl.1977. The 1970-1972-1974raptor surveys alongthe Trans-AlaskaOil Pipeline.pp. 199-221.In.' Chancellor,R.D. (ed.).World Conferenceon Birdsof Prey, Reportof the Proceedings.International Council for BirdPreservation. 440 pp. + appendices. SPATIAL RELATIONSHIPS OF NESTING GOLDEN EAGLES IN CENTRAL UTAH by DwightG. Smith• BiologyDepartment SouthernConnecticut State University New Haven, Connecticut 06515 and JosephR. Murphy Departmentof Zoology BrighamYoung University Provo, Utah 84602 Abstract We examinedthe distributionof GoldenEagle (Aquila chrysaetos)nest sites in the easternGreat Basinusing the Clark-Evansnearest-neighbor method of analysis.Distri- butionvalues indicated. uniform spacing of nestsites within the hills and ridges,which providedall of the potentialnesting sites in the studyarea. Analysis of GoldenEagle nestsite distributionwith three other large raptorssuggested a tendencytoward uni- form spacingbetween diurnal raptor speciesand aggregationwith the Great Horned Owl (Bubovirginianus). Introduction Odum(1971) suggested that populationsexhibit one of threedistribution patterns: (1) random,where habitat is homogenousand individualsdo not normallyinteract; (2) uni- form,where habitat is homogenousand individualscompete for one or moreresources; (3) aggregated,that mayresult from either heterogenous habitat or a tendencyto aggre- gatesocially. Newton (1979) noted that manyspecies exhibit uniform distribution of ter- ritoriesand nest sites except where available sites are limitedand concentrated,such as in the SnakeRiver Birds of PreyNatural Area. Our observationsof GoldenEagles in the easternGreat BasinDesert revealed a concentrationof nestsites in high, north-south orientedridges and hills but nonein interveningbroad, flat valleys.Herein we examine thisdistribution using the Clark-Evansnearest-neighbor model (1954). -
Hystrix Africaeaustralis)
Reproduction in captive female Cape porcupines (Hystrix africaeaustralis) R. J. van Aarde Mammal Research Institute, University ofPretoria, Pretoria 0002, South Africa Summary. Captive females attained sexual maturity at an age of 9\p=n-\16months and con- ceived for the first time when 10\p=n-\25months old. Adult females were polyoestrous but did not cycle while lactating or when isolated from males. The length of the cycle varied from 17 to 42 days (mean \m=+-\s.d. 31\m=.\2\m=+-\6\m=.\5days; n = 43) and females experienced 3\p=n-\7 sterile cycles before conceiving. Pregnancy lasted for 93\p=n-\94days (93\m=.\5\m=+-\0\m=.\6days; N = 4) and litter intervals varied from 296 to 500 days (385 \m=+-\60\m=.\4;n = 10). Litter size varied from 1 to 3 (1\m=.\5\m=+-\0\m=.\66;n = 165) and the well-developed precocial young weighed 300\p=n-\400g (351 \m=+-\47\m=.\4g; n= 19) at birth. Captive females reproduced throughout the year with most litters (78\m=.\7%;n = 165) being produced between August and March. Introduction Cape porcupines (Hystrix africaeaustralis) inhabit tropical forests, woodlands, grassland savannas, semi-arid and arid environments throughout southern Africa. Despite this widespread distribution little attention has been given to these nocturnal, Old World hystricomorph rodents, which shelter and breed in subterranean burrows, rock crevices and caves. Some information on reproduction in female porcupines has been published on the crested porcupine (H. cristata) (Weir, 1967), the Himalayan porcupine (H. hodgsoni) (Gosling, 1980) and the Indian porcupine (H. -
Genetic Structure of the North American Porcupine (Erethizon Dorsatum) Across Western Texas
GENETIC STRUCTURE OF THE NORTH AMERICAN PORCUPINE (ERETHIZON DORSATUM) ACROSS WESTERN TEXAS by Erica D. Thomas A Thesis Submitted in Partial Fulfillment Of the Requirements for the Degree MASTER OF SCIENCE Major Subject: Biology West Texas A&M University Canyon, Texas December 2017 Approved: Rocky Ward, PhD Date Chairman, Thesis Committee W. David Sissom, PhD Date Member, Thesis Committee William P. Johnson, M.S. Date Member, Thesis Committee W. David Sissom, PhD Date Department Head Dean, Academic College Date Angela N. Spaulding Date Dean, Graduate School ii ABSTRACT The North American porcupine (Erethizon dorsatum) is a highly mobile, generalist species with an extensive geographical distribution in North America. The porcupine was first documented in southwestern Texas in the early 20th century, but today occurs in most of the western two-thirds of the state. This species is relatively unstudied within the Great Plains ecoregion of North America, with no genetic studies having been conducted for this species in Texas. The objectives of this study were to describe population genetic metrics of porcupines across 3 ecoregions in western Texas by examining variation in 17 polymorphic microsatellites, and to confirm the applicability of the zinc finger protein sequencing method to identify sex in a population of North American porcupines. Tissue samples from 106 porcupines were collected from the High Plains, Rolling Plains, and Edwards Plateau ecoregions of western Texas. Sex was accurately identified for 92 porcupine tissue samples by directly sequencing a short portion (195 base pairs) of the zinc finger protein gene. Sixteen base pair substitutions between Zfx and Zfy chromosomes denoted the sex of individuals; heterozygous sequence for males (Zfx and Zfy), homozygous sequence for females (Zfx only). -
Response to CEQA Comments
Attachment 7: Response to CEQA comments Responses to verbal comments received during the 03/14/2019 Planning Commission Hearing on the Public Draft IS/MND/IEC document Comment Jeff Marcus -1 (PCE groundwater contamination and the Tahoe Asphalt Plant) Mr. Marcus stated concern about snow removal and American Disability Act (ADA) access. Mr. Marcus discussed general concern about repaving and dust control actions at the Tahoe Asphalt Plant, and stated concern about groundwater contamination, more specifically the health dangers of PCE. Lead Agency Response to Jeff Marcus (Verbal Comments 03/14/2019) The comments presented are not specific to the Project or project area. City general snow removal actions are part of the Operations and Maintenance Program. ADA access ramps are constructed with City-managed sidewalk and bike trail projects. Dust control measures must comply with El Dorado County Air Quality Management District Rule 223. The PCE contamination plume originates at Lake Tahoe Laundry Works at the Raley's Center and has migrated north towards Lake Tahoe (and remains outside of the Greenbelt and Bonanza portions of the project area) and at depths that extend below any 5-8 foot excavations that may be necessary for stormwater improvements on the north side of US Highway 50, should the plume direction change. Melanie Greene of Cardno, the firm that prepared the project-level analysis and environmental document, spoke to the information presented by Mr. Marcus related to PCE groundwater contamination, confirming that the Project posed no risk of exposing PCE contaminated groundwater. The South Tahoe “Y” PCE investigation and remediation efforts are in an adjacent catchment (west of the project boundary) and is a groundwater contamination issue from past use of dry cleaning solvents and metal degreasers containing tetrachloroethylene (PCE). -
Porcupine Wildlife Note
24. Porcupine The porcupine is a blackish, quill-armored, slow-moving rodent with an appetite for tree bark and salt. It lives in forests and often can be seen hunched into what appears to be a black ball high in a tree. While it does not occur in all parts of Pennsylvania, the porcupine is one of Pennsylvania’s best-known and most easily identified wild animals. Its taxonomic name is Erethizon dorsatum. The word “porcupine” comes from two Latin words, porcus (“swine”) and spina (“thorn”), which also reflects the species’ colloquial name, quill pig. In the East, porcupines inhabit Canada and New England south into Pennsylvania; they range through the northern Midwest and the Pacific Northwest, south in the forested Rocky Mountains nearly to Mexico, and north to Alaska. They live at all elevations from sea level to timberline. Biology Adult porcupines are about 30 inches in length, including a 6- to 10-inch tail. They weigh 9 to 15 pounds, with bigger, older adults weighing up to 20 pounds. Males are larger than females. The porcupine is North America’s second largest rodent; only the beaver is bigger. Porcupines have four incisors—two above and two below that are bright orange, strong and adapted to gnawing. Short-legged and stout, a porcupine has a pronounced arch to its back. Its skull is heavily constructed; the small, longest), yellow or white tipped with black, and lined with rounded head has a blunt muzzle, ears almost hidden in a foam-like material composed of many tiny air cells. An fur, and dull black eyes. -
Wolverines in Idaho 2014–2019
Management Plan for the Conservation of Wolverines in Idaho 2014–2019 Prepared by IDAHO DEPARTMENT OF FISH AND GAME July 2014 2 Idaho Department of Fish & Game Recommended Citation: Idaho Department of Fish and Game. 2014. Management plan for the conservation of wolverines in Idaho. Idaho Department of Fish and Game, Boise, USA. Idaho Department of Fish and Game – Wolverine Planning Team: Becky Abel – Regional Wildlife Diversity Biologist, Southeast Region Bryan Aber – Regional Wildlife Biologist, Upper Snake Region Scott Bergen PhD – Senior Wildlife Research Biologist, Statewide, Pocatello William Bosworth – Regional Wildlife Biologist, Southwest Region Rob Cavallaro – Regional Wildlife Diversity Biologist, Upper Snake Region Rita D Dixon PhD – State Wildlife Action Plan Coordinator, Headquarters Diane Evans Mack – Regional Wildlife Diversity Biologist, McCall Subregion Sonya J Knetter – Wildlife Diversity Program GIS Analyst, Headquarters Zach Lockyer – Regional Wildlife Biologist, Southeast Region Michael Lucid – Regional Wildlife Diversity Biologist, Panhandle Region Joel Sauder PhD – Regional Wildlife Diversity Biologist, Clearwater Region Ben Studer – Web and Digital Communications Lead, Headquarters Leona K Svancara PhD – Spatial Ecology Program Lead, Headquarters Beth Waterbury – Team Leader & Regional Wildlife Diversity Biologist, Salmon Region Craig White PhD – Regional Wildlife Manager, Southwest Region Ross Winton – Regional Wildlife Diversity Biologist, Magic Valley Region Additional copies: Additional copies can be downloaded from the Idaho Department of Fish and Game website at fishandgame.idaho.gov/wolverine-conservation-plan Front Cover Photo: Composite photo: Wolverine photo by AYImages; background photo of the Beaverhead Mountains, Lemhi County, Idaho by Rob Spence, Greater Yellowstone Wolverine Program, Wildlife conservation Society. Back Cover Photo: Release of Wolverine F4, a study animal from the Central Idaho Winter Recreation/Wolverine Project, from a live trap north of McCall, 2011. -
The Occurrence and Reestablishment of White-Tailed Eagle and Golden Eagle As Breeding Birds in Denmark
The occurrence and reestablishment of White-tailed Eagle and Golden Eagle as breeding birds in Denmark Erik EhmsEn, LEnnart PEdErsEn, hans meltoftE, tschErning cLausEn & timmE nyEgaard (Med et dansk resumé: Forekomst og genetablering af Havørn og Kongeørn som danske ynglefugle) Abstract Except for a number of largely unsuccessful breeding attempts during the second half of the 20th century, the White-tailed Eagle Haliaeetus albicilla had been absent as a breeding bird in Denmark for more than 80 years, when a popu- lation established itself during the second half of the 1990s. Released from persecution and contaminants the population has grown to 37 pairs in just 16 years. Reproductive success has grown with age and experience of the birds, so that the average number of fledged young per breeding pair peaked with almost two per pair 8-10 years after the establishment of each breeding pair. Similarly, the Golden Eagle Aquila chrysaetos reestablished a small population in Denmark from 1999 onwards after probably having bred here until about 150 years ago. For both species, this success was facilitated by conservation efforts including protection zones around eagle nests, monitoring and public outreach mainly carried out by volunteers from the Danish Ornithological Society / BirdLife Denmark. Introduction in former times, while the White-tailed Eagle bred in The reestablishment of White-tailed Eagle Haliaee- Denmark until it was driven extinct by persecution tus albicilla and Golden Eagle Aquila chrysaetos as in 1912 (Løppenthin 1967). The latter species made breeding birds in Denmark in the 1990s is one of a number of – usually unsuccessful – breeding at- the greatest achievements in modern Danish bird tempts during the second half of the 20th century, and nature conservation. -
Possible DRAFT Rule Language to Cover Taking Young
Attachment 3 DIVISION 55 FALCONRY LICENSES, PERMITS AND REQUIREMENTS 635-055-0000 Definition of Terms For the purpose of these rules, the following definitions apply: (1) "Captive bred" means any raptor, including eggs, hatched in captivity resulting from parents that mated in captivity, or are the progeny of artificial insemination. (2) "Falconry" is caring for and training raptors for pursuit of game, and the sport of hunting wild game with raptors. (3) “Indigenous raptor”, for purposes of falconry, means golden eagle (Aquila chrysaetos), sharp-shinned hawk (Accipter striatus), Cooper’s hawk (Accipter cooperii), northern goshawk (Accipter gentilis), red-tailed hawk (Buteo jamaicensis), American kestrel (Falco sparverius), merlin (Falco columbarius), prairie falcon (Falco mexicanus), peregrine falcon (Falco peregrinus), gyrfalcon (Falco rusticolus, and great horned owl (Bubo virginianus), (4) “Management or operational activities” means activities on nest-site structures (bridges or buildings) that are operational or maintenance actions to the structure deemed necessary by the structure owners or managers. These activities do not include nest entries for the purposes of banding birds for scientific purposes. (4) (5) “Passage” means first year migrant raptors capable of flight. (5) (6) “Post-fledgling” means a young first-year bird capable of flight which has recently flown from its nest. (6)(7) "Raptor" means any species or hybrid of the families Strigidae, Falconidae and Accipitridae. (7)(8) “Raptors at hack” means the intentional release of a raptor as a training technique, with the expectation of recapture after a period of time. (8)(9) "Take", for the purposes of these rules, means to trap, capture, or attempt to trap or capture a raptor from the wild for the purpose of falconry. -
Mammals of the Finger Lakes ID Guide
A Guide for FL WATCH Camera Trappers John Van Niel, Co-PI CCURI and FLCC Professor Nadia Harvieux, Muller Field Station K-12 Outreach Sasha Ewing, FLCC Conservation Department Technician Past and present students at FLCC Virginia Opossum Eastern Coyote Eastern Cottontail Domestic Dog Beaver Red Fox Muskrat Grey Fox Woodchuck Bobcat Eastern Gray Squirrel Feral Cat Red Squirrel American Black Bear Eastern Chipmunk Northern Raccoon Southern Flying Squirrel Striped Skunk Peromyscus sp. North American River Otter North American Porcupine Fisher Brown Rat American Mink Weasel sp. White-tailed Deer eMammal uses the International Union for Conservation of Nature (IUCN) for common and scientific names (with the exception of Domestic Dog) Often the “official” common name of a species is longer than we are used to such as “American Black Bear” or “Northern Raccoon” Please note that it is Grey Fox with an “e” but Eastern Gray Squirrel with an “a”. Face white, body whitish to dark gray. Typically nocturnal. Found in most habitats. About Domestic Cat size. Can climb. Ears and tail tip can show frostbite damage. Very common. Found in variety of habitats. Images are often blurred due to speed. White tail can overexpose in flash. Snowshoe Hare (not shown) is possible in higher elevations. Large, block-faced rodent. Common in aquatic habitats. Note hind feet – large and webbed. Flat tail. When swimming, can be confused with other semi-aquatic mammals. Dark, naked tail. Body brown to blackish (darker when wet). Football-sized rodent. Common in wet habitats. Usually doesn’t stray from water. Pointier face than Beaver. -
Predation by a Golden Eagle on a Brown Bear Cub
SHORT COMMUNICATION N Sørensen et al. Predation by a golden eagle on a brown bear cub Ole J. Sørensen1,4, Mogens Totsa˚ s2, Tore eagles attending bears. Murie hypothesized that Solstad2, and Robin Rigg3 eagles attending bears were waiting for opportunities to capture prey trying to escape from the bears. He 1North-Trondelag University College, Department of also observed eagles swooping at and diving low over Natural Resource Sciences and Information Technology, grizzlies and other carnivores, but interpreted this Box 2501, N-7729 Steinkjer, Norway behavior as play or curiosity, rather than predation. 2 Norwegian Nature Inspectorate, N-7485 Trondheim, C. McIntyre (US National Park Service, Fair- Norway 3 banks, Alaska, USA, personal communication, 2008), Slovak Wildlife Society, PO Box 72, 033 01 Liptovsky a golden eagle researcher in Denali National Park for Hradok, Slovakia many years, has never seen an eagle attack a bear, although she has often observed eagles following Abstract: During spring 2004 an adult female brown bears in open terrain, perhaps positioning themselves bear (Ursus arctos) and her 3 cubs-of-the-year were to take prey escaping from the bear as suggested by observed outside their den on a south-facing low- Murie. Commensalistic hunting, as well as curious or alpine slope in central Norway. They remained near play behavior by eagles in the vicinity of bears, could the den for 8–10 days and were, except for one day, be misinterpreted as eagles hunting, attacking, or observed daily by Totsa˚s and other wardens of the inspecting bears as possible prey. Predation by eagles Norwegian Nature Inspectorate. -
Porcupine, Tree
UWI The Online Guide to the Animals of Trinidad and Tobago Behaviour Coendou prehensilis (Tree Porcupine or Brazilian Porcupine) Family: Erethizontidae (New World Porcupines) Order: Rodentia (Rodents) Class: Mammalia (Mammals) Fig. 1. Brazilian porcupine, Coendou prehensilis. [http://animaldiversity.ummz.umich.edu/site/resources/pablo_goncalves/Coendou2a.jpg/view.html, downloaded 22 November 2011] TRAITS. Coendou prehensilis, the Brazilian porcupine, is a mid-sized rodent with evolutionarily modified body hair. This modified hair exists as keratin-toughened, needle-like, semi-hollow quills or spines that grow to approximately 6.5cm in length. Like all New World porcupines, spines grow singly out of the skin and possess minute barbs at the end of the shaft. These spines cover the entire body, except for its fleshy nose, its belly and a large portion of its prehensile tail, and are usually light in colour (white to burnished yellow); there are also darker brown to black (soft/ unmodified) hairs interspersed along the body. It has small round eyes; and, a rounded yet flattened snout. The snout is covered with very short and very fine hairs and has several long whiskers. The porcupine has two long incisors and the front of its mouth that grows continuously during life and lacks canine teeth. At adult weight, this porcupine can range from 2kg to 5kg (Roberts et al., 1984). The average length of an adult Brazilian porcupine is approximately 90cm with its tail contributing about half of that length. Coendou also has modified padded feet with four long clawed toes. At birth, the infants are approximately 50cm head to tail, 0.415kg, are covered in reddish brown hair and have soft natal quills about 1.5cm in length that harden a few days after it is born. -
Out of Europe: Investigating Hystrix Cristata (Rodentia: Hystricidae) Skull Morphometric Geographic Variability in Africa
Biogeographia – The Journal of Integrative Biogeography 36 (2021): a001 https://doi.org/10.21426/B636051379 Out of Europe: Investigating Hystrix cristata (Rodentia: Hystricidae) skull morphometric geographic variability in Africa FRANCESCO M. ANGELICI1*, PAOLO COLANGELO2, SPARTACO GIPPOLITI3 1 FIZV, Via Marco Aurelio 2, I-00184 Rome (Italy) 2 Consiglio Nazionale delle Ricerche, Istituto di Ricerca sugli Ecosistemi Terrestri, CNR-IRET, Via Salaria km 29.300, I-00015 Montelibretti, Rome (Italy) 3 Società Italiana per la Storia della Fauna ‘Giuseppe Altobello’, Viale Liegi 48, I-00198 Rome (Italy) * corresponding author: [email protected] Keywords: Crested porcupine, geographic variability, Hystrix cristata senegalica, Hystrix cristata galeata, North-East Africa, taxonomy. SUMMARY The crested porcupine Hystrix cristata is one of the most well-known members of the Family Hystricidae, yet very little is known regarding its geographic variability in Africa. Two alternative hypotheses exist; pre-1940s classical taxonomy supported the existence of a distinct Eastern African species, Hystrix galeata, whereas recent molecular data seem to support only a North-South separation inside one single species, with the geographic-ecological barrier represented by the Sahara desert. Our morphometric data support the recognition of Hystrix cristata senegalica Cuvier, 1822 as the sub- Saharan representative of the species with a clear morphological difference between the North African and sub-Saharan crested porcupines, which seem re-conductible mostly to size difference. Within H. c. senegalica, our analysis seems to support a weak separation between the West African and the East African samples. Owing to considerable qualitative skull differences and overlooked molecular data, the taxonomic status of H. galeata remains uncertain as well as the status of porcupines of North-East Africa (Nubia).