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© 2006 Abcteach.Com an Owl Is a Bird. There Are Two Basic Types of Owls: Typical Owls and Barn Owls. Owls Live in Almost Every
Reading Comprehension/ Animals Name _________________________________ Date ____________________ OWLS An owl is a bird. There are two basic types of owls: typical owls and barn owls. Owls live in almost every country of the world. Owls are mostly nocturnal, meaning they are awake at night. Owls are predators- they hunt the food that they eat. Owls hunt for mice and other small mammals, insects, and even fish. Owls are well adapted for hunting. Their soft, fluffy feathers make their flight nearly silent. They have very good hearing, which helps them to hunt well in the darkness. The sharp hooked beaks and claws of the owl make it very easy to tear apart prey quickly, although owls also eat some prey whole. Owl eyes are unusual. Like most predators, both of the owl’s eyes face front. The owl cannot move its eyes. Owls are far-sighted, which means they can see very well far away… but they can’t see up close very well at all. Fortunately, their distant vision is what they use for hunting, and they can see far away even in low light. Owls have facial disks around their eyes, tufts of feathers in a circle around each eye. These facial disks are thought to help with the owl’s hearing. Owls can turn their heads 180 degrees. This makes it look like they might be able to turn their heads all the way around, but 180 degrees is all the owl needs to see what’s going on all around him. Perhaps because of the owl’s mysterious appearance, especially its round eyes and flexible neck, there are a lot of myths and superstitions about owls. -
Do the Winter Diets of Sympatric Burrowing Owl and Short-Eared Owl Overlap in West-Central Mexico?
Proceedings of the Fourth International Partners in Flight Conference: Tundra to Tropics 96–101 DO THE WINTER DIETS OF SYMPATRIC BURROWING OWL AND SHORT-EARED OWL OVERLAP IN WEST-CENTRAL MEXICO? HÉCTOR E. VALDEZ-GÓMEZ,1,3 GEOFFREY L. HOLROYD,2 HELEN E. TREFRY,2 AND ARMANDO J. CONTRERAS-BALDERAS1 1Laboratorio de Ornitología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, Ciudad Universitaria CP 66451, A.P. 425 San Nicolás de los Garza, Nuevo León, México; and 2Environment Canada, Room 200, 4999-98 Avenue, Edmonton, Alberta T6B 2X3, Canada Abstract. Burrowing Owl (Athene cunicularia) and Short-eared Owl (Asio fl ammeus) are widely dis- tributed but uncommon species during winter in Mexico. Information about their winter ecology is limited, particularly in areas where both species are present. Knowledge of their diet is an important component to understand the nocturnal raptors’ habitat requirements. We analyzed 179 pellets of Burrowing Owl and 354 pellets of Short-eared Owl collected in 2002-2003, at the Military Airbase of Zapopan, Jalisco. The owls shared three main prey categories: invertebrates, small mammals, and birds. Small mammals provided the highest proportion of biomass in the Short-eared Owl diet and invertebrates in the Burrowing Owl diet. Food-niche breadth was lower in Short-eared than in Burrowing Owl refl ecting the diversity of invertebrates in the Burrowing Owl’s diet. The dietary overlap included items of relative low mass such as Northern Pigmy Mouse (Baiomys taylori) and the Gray Bird Grasshopper (Schistocerca nitiens). Zapopan Airbase is important for these two species and others adjacent to a large metropolitan city and should be managed as wildlife habitat that is compat- ible with its function for military training. -
Predator and Competitor Management Plan for Monomoy National Wildlife Refuge
Appendix J /USFWS Malcolm Grant 2011 Fencing exclosure to protect shorebirds from predators Predator and Competitor Management Plan for Monomoy National Wildlife Refuge Background and Introduction Background and Introduction Throughout North America, the presence of a single mammalian predator (e.g., coyote, skunk, and raccoon) or avian predator (e.g., great horned owl, black-crowned night-heron) at a nesting site can result in adult bird mortality, decrease or prevent reproductive success of nesting birds, or cause birds to abandon a nesting site entirely (Butchko and Small 1992, Kress and Hall 2004, Hall and Kress 2008, Nisbet and Welton 1984, USDA 2011). Depredation events and competition with other species for nesting space in one year can also limit the distribution and abundance of breeding birds in following years (USDA 2011, Nisbet 1975). Predator and competitor management on Monomoy refuge is essential to promoting and protecting rare and endangered beach nesting birds at this site, and has been incorporated into annual management plans for several decades. In 2000, the Service extended the Monomoy National Wildlife Refuge Nesting Season Operating Procedure, Monitoring Protocols, and Competitor/Predator Management Plan, 1998-2000, which was expiring, with the intent to revise and update the plan as part of the CCP process. This appendix fulfills that intent. As presented in chapter 3, all proposed alternatives include an active and adaptive predator and competitor management program, but our preferred alternative is most inclusive and will provide the greatest level of protection and benefit for all species of conservation concern. The option to discontinue the management program was considered but eliminated due to the affirmative responsibility the Service has to protect federally listed threatened and endangered species and migratory birds. -
A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes)
Galliform Baraminology 1 Running Head: GALLIFORM BARAMINOLOGY A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes) Michelle McConnachie A Senior Thesis submitted in partial fulfillment of the requirements for graduation in the Honors Program Liberty University Spring 2007 Galliform Baraminology 2 Acceptance of Senior Honors Thesis This Senior Honors Thesis is accepted in partial fulfillment of the requirements for graduation from the Honors Program of Liberty University. ______________________________ Timothy R. Brophy, Ph.D. Chairman of Thesis ______________________________ Marcus R. Ross, Ph.D. Committee Member ______________________________ Harvey D. Hartman, Th.D. Committee Member ______________________________ Judy R. Sandlin, Ph.D. Assistant Honors Program Director ______________________________ Date Galliform Baraminology 3 Acknowledgements I would like to thank my Lord and Savior, Jesus Christ, without Whom I would not have had the opportunity of being at this institution or producing this thesis. I would also like to thank my entire committee including Dr. Timothy Brophy, Dr. Marcus Ross, Dr. Harvey Hartman, and Dr. Judy Sandlin. I would especially like to thank Dr. Brophy who patiently guided me through the entire research and writing process and put in many hours working with me on this thesis. Finally, I would like to thank my family for their interest in this project and Robby Mullis for his constant encouragement. Galliform Baraminology 4 Abstract This study investigates the number of galliform bird holobaramins. Criteria used to determine the members of any given holobaramin included a biblical word analysis, statistical baraminology, and hybridization. The biblical search yielded limited biosystematic information; however, since it is a necessary and useful part of baraminology research it is both included and discussed. -
CONVERGENT EVOLUTION of ELANUS KITES and the OWLS Author(S): Juan J
CONVERGENT EVOLUTION OF ELANUS KITES AND THE OWLS Author(s): Juan J. Negro, Cino Pertoldi, Ettore Randi, Juan J. Ferrero, José M. López-Caballero, Domingo Rivera, and Erkki Korpimäki Source: Journal of Raptor Research, 40(3):222-225. 2006. Published By: The Raptor Research Foundation DOI: 10.3356/0892-1016(2006)40[222:CEOEKA]2.0.CO;2 URL: http://www.bioone.org/doi/full/10.3356/0892- 1016%282006%2940%5B222%3ACEOEKA%5D2.0.CO%3B2 BioOne (www.bioone.org) is an electronic aggregator of bioscience research content, and the online home to over 160 journals and books published by not-for-profit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. SHORT COMMUNICATIONS J. Raptor Res. 40(3):222–225 E 2006 The Raptor Research Foundation, Inc. CONVERGENT EVOLUTION OF ELANUS KITES AND THE OWLS JUAN J. NEGRO1 AND CINO PERTOLDI Estacio´n Biolo´gica de Don˜ana, Apdo. 1056, 41080 Sevilla, Spain ETTORE RANDI Istituto Nazionale per la Fauna Selvatica, 40064 Ozzano Emilia (BO), Italy JUAN J. -
Trip 17-Apr 18-Apr Havana Las Terrazas ANSERIFORMES: Anatidae Fulvous Whistling-Duck X Wood Duck X Blue-Winged Teal X Northern Pintail X Red-Breasted Merganser X
trip 17-Apr 18-Apr Havana Las Terrazas ANSERIFORMES: Anatidae Fulvous Whistling-Duck X Wood Duck X Blue-winged Teal X Northern Pintail X Red-breasted Merganser X PHOENICOPTERIFORMES: Phoenicopteridae American Flamingo X PODICIPEDIFORMES Least Grebe X SULIFORMES: Fregatidae Magnificent Frigatebird X SULIFORMES: Sulidae Brown Booby X SULIFORMES: Phalacrocoracidae Neotropic Cormorant X Double-crested Cormorant X SULIFORMES: Anhingidae Anhinga X PELECANIFORMES: Pelecanidae Brown Pelican X X X American White Pelican X PELECANIFORMES: Ardeidae Great Blue Heron X Great Egret X X Snowy Egret X X Little Blue Heron X X Tricolored Heron X Reddish Egret X Cattle Egret X X Green Heron X X Yellow-crowned Night-Heron X PELECANIFORMES: Threskiornithidae White Ibis X Glossy Ibis X Roseate Spoonbill X CATHARTIFORMES: Cathartidae Turkey Vulture X X X ACCIPITRIFORMES: Pandionidae Osprey X ACCIPITRIFORMES: Accipitridae Snail Kite X X Cuban Black Hawk X Red-tailed Hawk X X GRUIFORMES: Rallidae Common Gallinule X X CHARADRIIFORMES: Recurvirostridae Black-necked Stilt X American Avocet X CHARADRIIFORMES: Charadriidae Black-bellied Plover X Killdeer X CHARADRIIFORMES: Scolopacidae Ruddy Turnstone Stilt Sandpiper X Sanderling X Semipalmated Sandpiper X Short-billed Dowitcher X Spotted Sandpiper X X Solitary Sandpiper X Greater Yellowlegs X Lesser Yellowlegs X CHARADRIIFORMES: Laridae Laughing Gull X X Herring Gull X Least Tern X Royal Tern X X X Sandwich Tern X Black Skimmer X CHARADRIIFORMES: Stercocariidae Pomarine Jaeger X COLUMBIFORMES: Columbidae Rock Pigeon -
American Paleontologist Pages 1 and 4
FinalV OLUMEIssue 19, NUMBER 4 AMERICAN WINTER 2012 PALEONTOLOGIST A MAGAZINE OF EARTH SCIENCE PUBLISHED BY THE PALEONTOLOGICAL RESEARCH INSTITUTION AND ITS MUSEUM OF THE EARTH The Last Good Buy Birds in the New Age of Extinction Also in this issue... An Inordinate Fondness for Vertebrae page 20 Goodbye American Paleontologist pages 1 and 4 ...plus much more! US $5.00 FEATURE ARTICLE Th e Last Good Buy: Birds in the New Age of Extinction By Constance M. Soja Th e oldest fossils belonging to the undisputed bird survivors of the end-Mesozoic biodiversity crisis experienced Archaeopteryx date back 140-150 million years to the extraordinary evolutionary radiations. Co-adapting to the Mesozoic. During that geologic era, dinosaurs dominated brave new world, they fi lled vacated ecologic niches and terrestrial ecosystems around the globe. Pterosaurs – evolved into the iconic species that defi ne the Cenozoic – dinosaurs' evolutionary cousins, the fl ying reptiles – soared our modern world and Earth's current great geologic era. overhead, and an astounding variety of diminutive to gigantic With most animal and plant groups of the Mesozoic laid to aquatic reptiles – ichthyosaurs, plesiosaurs, pliosaurs, and rest, new species rose to dominance, and new competitive mosasaurs – cruised the world's oceans. Consuming squid- relationships were established. Oversized, fl ightless "terror like belemnoid and ammonoid prey, those top predators birds" – T. rex ultimate but down-sized body doubles – were also swam in the shallow seaways that fl ooded the interior pitted against fox- and pony-sized mammals, which in the of North America and other continents. Within 80 million previous 150 million years had been small, nocturnal, rat- years, the Cretaceous-Tertiary mass extinction that brought like animals eeking out a subsidiary existence. -
Herpetofauna and Aquatic Macro-Invertebrate Use of the Kino Environmental Restoration Project (KERP)
Herpetofauna and Aquatic Macro-invertebrate Use of the Kino Environmental Restoration Project (KERP) Tucson, Pima County, Arizona Prepared for Pima County Regional Flood Control District Prepared by EPG, Inc. JANUARY 2007 - Plma County Regional FLOOD CONTROL DISTRICT MEMORANDUM Water Resources Regional Flood Control District DATE: January 5,2007 TO: Distribution FROM: Julia Fonseca SUBJECT: Kino Ecosystem Restoration Project Report The Ed Pastor Environmental Restoration ProjectiKino Ecosystem Restoration Project (KERP) is becoming an extraordinary urban wildlife resource. As such, the Pima County Regional Flood Control District (PCRFCD) contracted with the Environmental Planning Group (EPG) to gather observations of reptiles, amphibians, and aquatic insects at KERP. Water quality was also examined. The purpose of the work was to provide baseline data on current wildlife use of the KERP site, and to assess water quality for post-project aquatic wildlife conditions. I additionally requested sampling of macroinvertebrates at Agua Caliente Park and Sweetwater Wetlands in hopes that the differences in aquatic wildlife among the three sites might provide insights into the different habitats offered by KERF'. The results One of the most important wildlife benefits that KERP provides is aquatic habitat without predatory bullfrogs and non- native fish. Most other constructed ponds and wetlands in Tucson, such as the Sweetwater Wetlands and Agua Caliente pond, are fuIl of non-native predators which devastate native fish, amphibians and aquatic reptiles. The KERP Wetlands may provide an opportunity for reestablishing declining native herpetofauna. Provided that non- native fish, bullfrogs or crayfish are not introduced, KERP appears to provide adequate habitat for Sonoran Mud Turtles (Kinosternon sonoriense), Lowland Leopard Frogs (Rana yavapaiensis), and Mexican Gartersnakes (Tharnnophis eques) and Southwestern Woodhouse Toad (Bufo woodhousii australis). -
Aullwood's Birds (PDF)
Aullwood's Bird List This list was collected over many years and includes birds that have been seen at or very near Aullwood. The list includes some which are seen only every other year or so, along with others that are seen year around. Ciconiiformes Great blue heron Green heron Black-crowned night heron Anseriformes Canada goose Mallard Blue-winged teal Wood duck Falconiformes Turkey vulture Osprey Sharp-shinned hawk Cooper's hawk Red-tailed hawk Red-shouldered hawk Broad-winged hawk Rough-legged hawk Marsh hawk American kestrel Galliformes Bobwhite Ring-necked pheasant Gruiformes Sandhill crane American coot Charadriformes Killdeer American woodcock Common snipe Spotted sandpiper Solitary sandpiper Ring-billed gull Columbiformes Rock dove Mourning dove Cuculiformes Yellow-billed cuckoo Strigiformes Screech owl Great horned owl Barred owl Saw-whet owl Caprimulgiformes Common nighthawk Apodiformes Chimney swift Ruby-throated hummingbird Coraciformes Belted kinghisher Piciformes Common flicker Pileated woodpecker Red-bellied woodpecker Red-headed woodpecker Yellow-bellied sapsucker Hairy woodpecker Downy woodpecker Passeriformes Eastern kingbird Great crested flycatcher Eastern phoebe Yellow-bellied flycatcher Acadian flycatcher Willow flycatcher Least flycatcher Eastern wood pewee Olive-sided flycatcher Tree swallow Bank swallow Rough-winged swallow Barn swallow Purple martin Blue jay Common crow Black-capped chickadee Carolina chickadee Tufted titmouse White-breasted nuthatch Red-breasted nuthatch Brown creeper House wren Winter wren -
The Burrowing Owl Athene Cunicularia Gained Its Name from a Particular Behaviour: It Nests Underground
Introduction This owl • is smaller than a pigeon • hunts as much in the day as at night in the summer • mimics the hiss of a rattlesnake • is one of the most endangered birds in western Canada Description The Burrowing Owl Athene cunicularia gained its name from a particular behaviour: it nests underground. But contrary to the impression given by the bird’s scientific name, which means “little digger,” this owl rarely digs its own burrow. Instead, it constructs its nest in burrows vacated by small mammals like ground squirrels, badgers, and prairie dogs. The adult Burrowing Owl is smaller than a pigeon. It weighs between 125 and 185 g and stands from 19 to 20 cm tall. Its body is generally brown, mottled with white flecks and barred across the chest. This earth-coloured plumage provides good camouflage in the grasslands where the owl lives. The Burrowing Owl’s head is rounded, and its eyes and beak are yellow. The sexes look similar, but the male is slightly lighter in colour. While they resemble the adults for the most part, the young have rusty-coloured throats and buff-coloured breasts without barring; they acquire their adult-like plumage during the late summer. Signs and sounds To discourage predators, the Burrowing Owl can make a noise like the rattling hiss of a rattlesnake’s tail. Males will repeat a doleful coo-coooo, mainly to attract females. Otherwise, Burrowing Owls make a variety of sounds to each other that are rarely heard by humans. Habitats and Habits On the dry short-grass prairie, the Burrowing Owl is found on flat-to-gently-undulating, treeless plains. -
Town of Superior Raptor Monitoring 2019 Summary
Town of Superior Raptor Monitoring 2019 Summary Sponsored by the Open Space Advisory Committee Introduction: In late 2018, the Town of Superior Open Space Advisory Committee initiated a program to monitor the presence and activity of raptors (eagles, hawks, falcons, and owls) in and near Superior. The program has several goals: determining what raptor species are present in Superior, learning what areas raptors use at different times of the year, monitoring any nesting activity, working to prevent unnecessary disturbance to raptors, identifying habitats to protect, and providing relevant education to the Town’s residents. Nine volunteer observers, all Superior residents, monitored seven general locations approximately weekly during the 2019 nesting season and identified eight species of raptors in the target areas. Some of these species use open spaces in Superior only intermittently, for hunting or migration. However, monitors determined that four species nested in or adjacent to Superior in 2019; ten nests were located and at least nine of them produced fledglings. The nesting species were Great Horned Owl, Red-tailed Hawk, Cooper’s Hawk, and American Kestrel. Background: Southeast Boulder County, and especially the prairie dog colonies along Rock Creek west of Hwy 36, historically supported significant densities of several raptor species, especially during winter. As late as the mid-1980s, winter bird counts showed that our area had one of the highest populations of Ferruginous Hawks in the entire U.S. [3,4]. With the loss of open space due to increasing development in the 1990s and the additional reduction of prairie dogs due to intermittent plague epidemics, populations of large open-country raptors in Figure 1 - Cooper's Hawk by Barbara Pennell and near Superior declined precipitously [2]. -
Evolution of the Barred Owl Threat to the Northern Spotted Owl
Timeline: Evolution of the Barred Owl Threat to the Northern Spotted Owl Full literature citations are listed alphabetically by author at the end of this fact sheet. 1959: Barred owls, native to eastern North America, are first documented in the northern parts of the northern spotted owl’s range in British Columbia. They appear to have moved westward from the Northeastern U.S. into British Columbia and then south into Washington. 1970s: Barred owls are first documented within the range of the spotted owl in Oregon (in 1972), Washington (in 1973), and California (in 1976). 1988: A thesis on barred owl and spotted owl ranges shows barred owls are “generalists” compared to spotted owls because they use a variety of habitats and forage on a broader range of prey. [Hamer, Thomas, “Barred Owl and Spotted Owl Home Ranges and Habitat Use in Washington”] 1989: A status review for the spotted owl indicates that the long-term impact of barred owl expansion into the range of the spotted owl is unknown but of considerable concern. [USFWS, “The Northern Spotted Owl Status Review Supplement”] 1990: U.S. Fish and Wildlife Service (FWS) lists the northern spotted owl under the Endangered Species Act as a threatened species in Washington, Oregon, and California. Habitat loss is identified as the primary threat to spotted owls. The listing documents reflect concerns raised in the previous year’s status review about barred owl expansion. 1994: Northwest Forest Plan is finalized, in part to guide federal agencies’ contribution to spotted owl conservation throughout the owl’s range. The plan amends federal resource management plans within 19 National Forests (19.4 million acres) and seven BLM districts (2.7 million acres).