BURROWING OWL (Athene Cunicularia) Jennifer A
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Prey Ecology of the Burrowing Owl Athene Cunicularia Cunicularia (Molina, 1782) on the Northern Coast of Santa Catarina, Brazil
Studies on Neotropical Fauna and Environment ISSN: (Print) (Online) Journal homepage: https://www.tandfonline.com/loi/nnfe20 Prey ecology of the burrowing owl Athene cunicularia cunicularia (Molina, 1782) on the northern coast of Santa Catarina, Brazil Alana Drielle Rocha , J. O. Branco & G. H. C. Barrilli To cite this article: Alana Drielle Rocha , J. O. Branco & G. H. C. Barrilli (2021): Prey ecology of the burrowing owl Athenecuniculariacunicularia (Molina, 1782) on the northern coast of Santa Catarina, Brazil, Studies on Neotropical Fauna and Environment To link to this article: https://doi.org/10.1080/01650521.2020.1867953 Published online: 13 Jan 2021. Submit your article to this journal View related articles View Crossmark data Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=nnfe20 STUDIES ON NEOTROPICAL FAUNA AND ENVIRONMENT https://doi.org/10.1080/01650521.2020.1867953 ORIGINAL ARTICLE Prey ecology of the burrowing owl Athene cunicularia cunicularia (Molina, 1782) on the northern coast of Santa Catarina, Brazil Alana Drielle Rocha a, J. O. Branco b and G. H. C. Barrilli a aDepartment of Biological and Health Sciences, Federal University of São Carlos, São Carlos, Brazil; bSchool of the Sea, Science and Technology, Vale do Itajaí University, Itajaí, Brazil ABSTRACT ARTICLE HISTORY We analyzed the diet of Athene cunicularia cunicularia in order to identify and compare prey items Received 14 August 2020 in dune populations in Santa Catarina, Brazil: Interpraias (INT), Praia Brava (BRA), Praia Central Accepted 20 December 2020 (NAV) and Peninsula (BVE). Due to the characteristics of urbanization in these regions, we hypothesized that there would be greater abundance and consumption of urban insect pests KEYWORDS Burrowing owl; dunes; diet; in the areas of BRA, NAV, and INT than in BVE. -
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. -
Hawk-Owls and Allies Genus Ninox Hodgs
Text extracted from Gill B.J.; Bell, B.D.; Chambers, G.K.; Medway, D.G.; Palma, R.L.; Scofield, R.P.; Tennyson, A.J.D.; Worthy, T.H. 2010. Checklist of the birds of New Zealand, Norfolk and Macquarie Islands, and the Ross Dependency, Antarctica. 4th edition. Wellington, Te Papa Press and Ornithological Society of New Zealand. Pages 264-265. Order STRIGIFORMES: Owls Regarding the following nomina dubia, see under genus Aegotheles Vigors & Horsfield: Strix parvissima Ellman, 1861: Zoologist 19: 7465. Nomen dubium. Strix parvissima Potts, 1871: Trans. N.Z. Inst. 3: 68 – Rangitata River, Canterbury. Nomen dubium. Athene (Strix) parvissima Potts; Potts 1873, Trans. N.Z. Inst. 5: 172. Nomen dubium Family STRIGIDAE Leach: Typical Owls Strigidae Leach, 1819: Eleventh room. In Synopsis Contents British Museum 15th Edition, London: 64 – Type genus Strix Linnaeus, 1758. Subfamily BUBONINAE Vigors: Hawk-owls and Allies Bubonina Vigors, 1825: Zoological Journal 2: 393 – Type genus Bubo Dumeril, 1805. Genus Ninox Hodgson Ninox Hodgson, 1837: Madras Journ. Lit. Sci. 5: 23 – Type species (by original designation) Ninox nipalensis Hodgson = Ninox scutulata lugubris (Tickell). Hieracoglaux Kaup, 1848: Isis von Oken, Heft 41: col. 768 – Type species (by subsequent designation) Falco connivens Latham = Ninox connivens (Latham). As a subgenus of Ninox. Spiloglaux Kaup, 1848: Isis von Oken, Heft 41: col. 768 – Type species (by subsequent designation) Strix boobook Latham = Ninox boobook (Latham). As a subgenus of Ninox. Ieraglaux Kaup, 1852: in Jardine, Contrib. Ornith.: 107 – Type species (by subsequent designation) Falco connivens Latham = Ninox connivens (Latham). Rhabdoglaux Bonaparte, 1854: Revue Mag. Zool. 2 (2): 543 – Type species (by subsequent designation) Athene humeralis Bonaparte = Ninox rufa humeralis (Bonaparte). -
Pre–Release Training of Juvenile Little Owls Athene Noctua to Avoid Predation
Animal Biodiversity and Conservation 34.2 (2011) 389 Pre–release training of juvenile little owls Athene noctua to avoid predation R. Alonso, P. Orejas, F. Lopes & C. Sanz Alonso, R., Orejas, P., Lopes, F. & Sanz, C., 2011. Pre–release training of juvenile little owls Athene noctua to avoid predation. Animal Biodiversity and Conservation, 34.2: 389–393. Abstract Pre–release training of juvenile little owls Athene noctua to avoid predation.— Anti–predator training of juvenile little owls was tested in a sample of recovered owls raised in captivity in Brinzal Owl Rescue Center (Madrid, Spain). Mortality caused by predators has been described previously in released individuals. Nine little owls were conditioned during their development to a naturalized goshawk and a large live rat, whose presence was paired to the owl’s alarm call. All nine owls and seven non–trained individuals were then released during the late summer and autumn and radio–tracked for six weeks to test their survival. In total 71.4% of the trained owls survived while only the 33.3% of the untrained group were alive at the end of week six. The only cause of death that was detected was predation. Antipredator training, therefore, seems to be beneficial in maximizing survival after the release of juvenile little owls. Key words: Little owl, Athene noctua, Reintroduction, Release, Survival, Antipredator training. Resumen Entrenamiento antes de la liberación en mochuelos europeos Athene noctua para evitar su depredación.— Un entrenamiento sobre mochuelos juveniles para evitar la depredación, se ha testado en una muestra de ejem- plares recuperados y criados en el Centro de Recuperación de Rapaces Nocturnas Brinzal (Madrid, España). -
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). -
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]. -
Seasonal Food Habits of Burrowing Owls (Athene Cunicularia) in Human-Altered Landscapes
SEASONAL FOOD HABITS OF BURROWING OWLS (ATHENE CUNICULARIA) IN HUMAN-ALTERED LANDSCAPES A Thesis presented to the Faculty of California Polytechnic State University, San Luis Obispo In Partial Fulfillment of the Requirements for the Degree Master of Science in Biological Sciences by Carie Marie Wingert May 2012 © 2012 Carie Marie Wingert ALL RIGHTS RESERVED ii COMMITTEE MEMBERSHIP TITLE: Seasonal Food Habits of Burrowing Owls (Athene cunicularia) in Human-altered Landscapes AUTHOR: Carie Marie Wingert DATE SUBMITTED: May 2012 COMMITTEE CHAIR: Dr. John Perrine, Assistant Professor COMMITTEE MEMBER: Dr. Emily Taylor, Associate Professor COMMITTEE MEMBER: Dr. Brian Cypher, Adjunct Professor: CSU- Stanislaus iii ABSTRACT SEASONAL FOOD HABITS OF BURROWING OWLS (ATHENE CUNICULARIA) IN HUMAN-ALTERED LANDSCAPES Carie Marie Wingert In 2004, I initiated a year-long study to investigate the food habits of burrowing owls (Athene cunicularia). Burrowing owls have been found in a variety of human-altered landscapes; however, little is known about burrowing owl food habits in urban landscapes. Burrowing owl food habits during the non-breeding season are also largely undocumented, despite increasing concern over the survival of overwintering burrowing owls. Differences in prey consumption between reproductive and non-reproductive owls during the breeding season have not yet been examined. I collected pellets over a 12 month period at four study sites affected by different levels of human alteration in the southern San Joaquin Valley of California. Data was collected at four study sites representing natural (Wind Wolves), semi-natural (Allensworth Ecological Reserve), agricultural (Friant Kern Canal), and urban (Bakersfield) landscapes. Invertebrates, primarily ground dwelling insects, were the most commonly consumed prey type, found in 96% of all pellets examined. -
Strigiformes) and Lesser Nighthawks (Chodeiles Acutipennis
UNIVERSITY OF CALIFORNIA RIVERSIDE The Evolution of Quiet Flight in Owls (Strigiformes) and Lesser Nighthawks (Chodeiles acutipennis) A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Evolution, Ecology, and Organismal Biology by Krista Le Piane December 2020 Dissertation Committee: Dr. Christopher J. Clark, Chairperson Dr. Erin Wilson Rankin Dr. Khaleel A. Razak Copyright by Krista Le Piane 2020 The Dissertation of Krista Le Piane is approved: Committee Chairperson University of California, Riverside ACKNOWLEDGEMENTS I thank my Oral Exam Committee: Dr. Khaleel A. Razak (chairperson), Dr. Erin Wilson Rankin, Dr. Mark Springer, Dr. Jesse Barber, and Dr. Scott Curie. Thank you to my Dissertation Committee: Dr. Christopher J. Clark (chairperson), Dr. Erin Wilson Rankin, and Dr. Khaleel A. Razak for their encouragement and help with this dissertation. Thank you to my lab mates, past and present: Dr. Sean Wilcox, Dr. Katie Johnson, Ayala Berger, David Rankin, Dr. Nadje Najar, Elisa Henderson, Dr. Brian Meyers Dr. Jenny Hazelhurst, Emily Mistick, Lori Liu, and Lilly Hollingsworth for their friendship and support. I thank the Natural History Museum of Los Angeles County (LACM), the California Academy of Sciences (CAS), Museum of Vertebrate Zoology (MVZ) at UC Berkeley, the American Museum of Natural History (ANMH), and the Natural History Museum (NHM) in Tring for access to specimens used in Chapter 1. I would especially like to thank Kimball Garrett and Allison Shultz for help at LACM. I also thank Ben Williams, Richard Jackson, and Reddit user NorthernJoey for permission to use their photos in Chapter 1. Jessica Tingle contributed R code and advice to Chapter 1 and I would like to thank her for her help. -
Phylogenetic Relationships in Owls Based on Nucleotide Sequences of Mitochondrial and Nuclear Marker Genes
Chancellor, R. D. & B.-U. Meyburg eds. 2004 Raptors Worldwide WWGBP/MME Phylogenetic Relationships in Owls based on nucleotide sequences of mitochondrial and nuclear marker genes Michael Wink, Hedi Sauer-Gürth & Marc Fuchs ABSTRACT Together with morphological and vocal characters, nucleotide sequences help to define phylogenetic relationships in owls. Since owls are nocturnal their morphological traits are often very similar a systematic differentiation or speciation event can easily be overlooked. A recent example is Ninox sumbaensis from the island of Sumba. An unknown owl that had been observed there had been assumed to be a member of Otus. DNA data unequivocally showed (Olsen et al. 2002) that it belongs to the genus Ninox. It was named Ninox sumbaensis. About 80 species of the Strigidae and 16 species of Tytonidae have been studied so far in our laboratory and a phylogeny based on cytochrome b data has been published (Wink & Heidrich 1999). We have enlarged our cytochrome b data base and additionally have sequenced a nuclear marker (LDHb intron DNA). Basically, the ncDNA data support the results obtained from mtDNA. INTRODUCTION Since owls are nocturnal their morphological traits ^re often very similar (König et al, 1999) a systematic differentiation or speciation event can easily be overlooked. Together with morphological and vocal characters nucleotide sequences of marker genes help to define phylogenetic relationships in owls. Nucleotide sequences of the mitochondrial cytochrome b gene have already been employed to study the systematics and evolution of diurnal raptors and owls (Griffiths 1997; Mindell 1997; Groombridge et al. 2002, Krucken-hauser et al, 2003, Riesing et al, 2003; from our laboratory: Seibold et al, 1993, 1996; Heidrich & Wink 1994, 1998; Heidrich étal., 1995a,b, 1996; Wink 1995, 1998, 2000; Wink & Seibold 1996; Wink & Sauer-Gürth 2000; Wink et al. -
Natural History and Protection of Burrowing Owis
NATURAL HISTORY AND PROTECTION OF BURROWING OWIS CLARKS. WINCHELL, Natural Resources Office, Naval Air Station North Island, P.O. Box 357040, San Diego, California 92135. ABSTRACT: Burrowing owls (Speotyto cunicularia) were monitored over a four year period at Naval Air Station North Island, a developed area at the north end of San Diego Bay, California. Protection of the nest burrows and a burrow marking program were initiated in 1991. The breeding population increased from 14 to 27 nests after this marking program began. Burrow types and ways to differentiate burrows used by owls from those used by California ground squirrels (Spermophilus beecheyi) are outlined. The importance of burrows and their management is discussed with reference to the natural history of the owl. Proc. 16th Vcrtcbr. Pest Conf. (W.S. Halverson& A.C. Crabb, Eds.) Published at Univ. of Calif., Davis. 1994. INTRODUCTION NATURAL HISTORY Burrowing owls (Speotyto cu11icularia) are semi Burrowing owls range from North America, southern colonial nesting raptors whose densities depend on a Canada and western United States, into South America, commensal relationship with rodents that maintain southern Argentina and western Chile. An isolated complex burrow systems. In southern California, subspecies occurs in the southern panhandle of Florida burrowing owls depend upon California ground squirrels and West Indies (Bent 1938). The species is migratory (Spermophilus beecheyi) to develop such systems. Since throughout the northern portion of its range, however, in the early 1970s, burrowing owl populations have been southern California burrowing owls are year round reported in decline (Zam 1974, Collins 1979), where the residents. In the United States, this non-migratory pattern primary causes have been loss of habitat (Howie 1980) begins in central California, extends along the coast and and rodent control (Butts 1973). -
Use of Mammal Manure by Nesting Burrowing Owls: a Test of Four Functional Hypotheses
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln USGS Staff -- Published Research US Geological Survey 2006 Use of mammal manure by nesting burrowing owls: a test of four functional hypotheses Matthew D. Smith University of Arizona, [email protected] Courtney J. Conway University of Arizona, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/usgsstaffpub Part of the Geology Commons, Oceanography and Atmospheric Sciences and Meteorology Commons, Other Earth Sciences Commons, and the Other Environmental Sciences Commons Smith, Matthew D. and Conway, Courtney J., "Use of mammal manure by nesting burrowing owls: a test of four functional hypotheses" (2006). USGS Staff -- Published Research. 571. https://digitalcommons.unl.edu/usgsstaffpub/571 This Article is brought to you for free and open access by the US Geological Survey at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in USGS Staff -- Published Research by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. ANIMAL BEHAVIOUR, 2007, 73,65e73 doi:10.1016/j.anbehav.2006.05.012 Use of mammal manure by nesting burrowing owls: a test of four functional hypotheses MATTHEW D. SMITH & COURTNEY J. CONWAY USGS Arizona Cooperative Fish and Wildlife Research Unit, School of Natural Resources, The University of Arizona, Tucson (Received 30 August 2005; initial acceptance 30 November 2005; final acceptance 24 May 2006; published online 2 November 2006; MS. number: A10234) Animals have evolved an impressive array of behavioural traits to avoid depredation. Olfactory camouflage of conspicuous odours is a strategy to avoid depredation that has been implicated only in a few species of birds.