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Diet of Three Sympatric Owls in Steppe Habitats of Eastern Kazakhstan
256 SHORT COMMUNICATIONS VOL. 37, NO. 3 Comfin en Espafia y Portugal (I Censo Coordinado). (Oypaetusbarbaras) en Catalufia (NE Espafia) e imph- Afio 2000. Monograf/a nø 8. SEO/BirdLife, Madrid, caciones sobre su conservacitn. Do•ana Acta Vertebr Spain. 24:235-243. DONAZAR,J.A. 1993. Los buitres ib•ricos. Biologla y con- PAm½ER,P.G., T.A. WAITE, AND M.D. DECKER. 1995. Kin- servacitn. J.M. Reyero, Madrid, Spain. ship and associationin communally roosting black --, O. CEBALLOS,AND J.L. TELLA. 1996. Communal vultures. Anita. Behar. 49:395-401. roostsof EgyptianVultures (Neophronpercnopterus): dy- RABENOLD, P.P. 1983. The communal roost in Black and namics and implicationsfor the speciesconservation. Turkey Vultures:an Information Center?Pages 303- Pages 189-201 in J. Muntaner and J. Mayol [EDS.], 321 in S.R. Wilbur and J.A. Jackson [EDS.], Vulture Biologia y Conservaci0n de las Rapaces Mediterr•- biology and management. Univ. of California Press, neas. Monografias No. 4 de la SEO, Madrid, Spain. Berkeley, CA U.S.A. ß 1987. Recruitment to food in black vultures: ev- --, c.J. PAI,ACIOS,L. GANOOSO,O. CEBALLOS,M.J. GONZ./•LEZ,AND F. HIRALDO. 2002. Conservation status idence for following from communal roosts.Anita. Be- hay. 35:1775-1785. and limiting factorsin the endangeredpopulation of TELLA,J.L. 1991. Dormideros de alimoches en el Valle EgyptianVulture (Neophronpercnopterus) in the Canary Islands. Bid. Conserv. 107:89-98. Medio del Ebro. ActasI CongresoInternacional sobre Aves Carrofieras: 69-74. AEDENAT-CODA, Madrid, MAROAL•D^,A. 1997. Aparici6n de un dormidero comu- Spain. nal de Alimoche (Neophronpercnopterus) en Catalufia ß 2001. -
A Type of Owl Called Asio Flammeus
ADW: Asio flammeus: Information Page I of 8 -i - • Structured Inquiry Searct Home > Kingdom Animalia Phylum Chordata A Subphylum Vertebrata 0 Class Aves > Order Strigiformes P Family Strigidae > Species Asio flammeus Asio flammeus short-eared owl Information Pictures Classification 2008/0/20 02 :22:23. 076 IJS/Eastern By Nathan Doan Geographic Range Kingdom: Animalia Phylum: Chordata Subphylum: Vertebrata Class: Aves Order: Strigiformes Family: Strigidae IGenus: Asio Species: Asio flammeus Short-eared owls are one of the world's most. widely distributed owls. They inhabit all of North and South America; this area includes the coast of the Arctic Ocean to Pantagonia. Short-eared owls can also be found on every continent except Australia and Antarctica. (Granlund et al., 1994; Welty, 1975;' Pearson, 1936) Biogeographic Regions: nearctic k (native CL); palearctic CL (native q); oriental Q. (native Q,); ethiopian CL (native k); neotropical q (native CL). Other Geographic Terms: cosmopolitan Q. Habitat One of the world's most widely distributed owls, Asio flammeus 'can be found throughout much of North America and Eurasia. These owls prefer to live inI marshes and bogs; they inhabit open, treeless areas. Their hunting and nesting habits Make them well suited to relatively flat land. This species is migratory but uses relativelY similar habitats during summer and winter. Short-eared owls have specialized eating habits and tend to stay http://animaldiversity.ummz.umich. edu/site/accounts/informationlAsio-flammeus.html 1/23/2008 ADW: Asio flammeus: Information Page 2 of 8 where they can find ample food. They will leave an area to find preferred prey rather than eat other animals. -
A. Gosler Publications: 2013. Book Chapter. Gosler, A.G., Bhagwat, S., Harrop, S., Bonta, M. & Tidemann, S. (2013) Chapter 6
A. Gosler Publications: 2013. Book chapter. Gosler, A.G., Bhagwat, S., Harrop, S., Bonta, M. & Tidemann, S. (2013) Chapter 6: Leadership and listening: inspiration for conservation mission and advocacy. In Macdonald, D. & Willis, K.J. (eds) Key Topics in Conservation Biology 2. J. Wiley & Sons, Ltd., Oxford. In Press. 2013. Advice Note to SCB Policy Committee. Lee J, Gosler AG, Vyas D, Schaefer J, Chong KY, Kahumbu P, Awoyemi SM & Baugh T. Religion and Conservation Research Collaborative (RCRC) of the Religion and Conservation Biology Working Group (RCBWG) Society for Conservation Biology (SCB)’s Position on the Use of Ivory for Religious Objects. ....................................................................................................... 2012. Letter to Editor. Awoyemi, S.M., Gosler, A.G., Ho, I., Schaefer, J. & Chong, KY. Mobilizing Religion and Conservation in Asia. Science 338: 1537-1538. [doi: 10.1126/science.338.6114.1537-b] 2012. Advice note to SCB Policy Committee. Awoyemi SM, Schaefer J, Gosler A, Baugh T, Chong KY & Landen E. Religion and Conservation Research Collaborative (RCRC) of the Religion and Conservation Biology Working Group (RCBWG) Society for Conservation Biology (SCB)’s Position on the Religious Practice of Releasing Captive Wildlife for Merit. 2012. Scientific Paper. Briggs BD, Hill DA & Gosler AG*. Habitat selection and waterbody-complex use by wintering Gadwall and Shoveler in South West London: implications for the designation and management of multi-site protected areas. Journal for Nature Conservation, 20, 200- 210. [doi: 10.1016/j.jnc.2012.04.002] 2012. Advice note to Libyan National Assembly. Environmental Security in the Libyan Constitution. 2012. Scientific Paper. Bulla M, Šálek M, Gosler AG. Eggshell spotting does not predict male incubation, but marks thinner areas of a shorebird’s shells. -
Indicators of Biodiversity for Ecologically Sustainable Forest Management
Essays Indicators of Biodiversity for Ecologically Sustainable Forest Management DAVID B. LINDENMAYER,* CHRIS R. MARGULES,† AND DANIEL B. BOTKIN‡ *Centre for Resource and Environmental Studies & Department of Geography, The Australian National University, Canberra, ACT 0200, Australia, email [email protected] †CSIRO Division of Wildlife and Ecology, GPO Box 284, Canberra, ACT 2601, Australia, email [email protected] ‡George Mason University, Fairfax, VA 22202, and The Center for the Study of the Environment, P.O. Box 6945, Santa Barbara, CA 93160, U.S.A., email [email protected] Abstract: The conservation of biological diversity has become one of the important goals of managing for- ests in an ecologically sustainable way. Ecologists and forest resource managers need measures to judge the success or failure of management regimes designed to sustain biological diversity. The relationships between potential indicator species and total biodiversity are not well established. Carefully designed studies are re- quired to test relationships between the presence and abundance of potential indicator species and other taxa and the maintenance of critical ecosystem processes in forests. Other indicators of biological diversity in forests, in addition or as alternatives to indicator species, include what we call structure-based indicators. These are stand-level and landscape-level (spatial) features of forests such as stand structural complexity and plant species composition, connectivity, and heterogeneity. Although the adoption of practices to sustain (or recreate) key characteristics of forest ecosystems appear intuitively sensible and broadly consistent with cur- rent knowledge, information is lacking to determine whether such stand- and landscape-level features of for- ests will serve as successful indices of (and help conserve) biodiversity. -
Status and Diet of the European Shag (Mediterranean Subspecies) Phalacrocorax Aristotelis Desmarestii in the Libyan Sea (South Crete) During the Breeding Season
Xirouchakis et alContributed.: European ShagPapers in the Libyan Sea 1 STATUS AND DIET OF THE EUROPEAN SHAG (MEDITERRANEAN SUBSPECIES) PHALACROCORAX ARISTOTELIS DESMARESTII IN THE LIBYAN SEA (SOUTH CRETE) DURING THE BREEDING SEASON STAVROS M. XIROUCHAKIS1, PANAGIOTIS KASAPIDIS2, ARIS CHRISTIDIS3, GIORGOS ANDREOU1, IOANNIS KONTOGEORGOS4 & PETROS LYMBERAKIS1 1Natural History Museum of Crete, University of Crete, P.O. Box 2208, Heraklion 71409, Crete, Greece ([email protected]) 2Institute of Marine Biology, Biotechnology & Aquaculture, Hellenic Centre for Marine Research (HCMR), P.O. Box 2214, Heraklion 71003, Crete, Greece 3Fisheries Research Institute, Hellenic Agricultural Organization DEMETER, Nea Peramos, Kavala 64007, Macedonia, Greece 4Department of Biology, University of Crete, P.O. Box 2208, Heraklion 71409, Crete, Greece Received 21 June 2016, accepted 21 September 2016 ABSTRACT XIROUCHAKIS, S.M., KASAPIDIS, P., CHRISTIDIS, A., ANDREOU, G., KONTOGEORGOS, I. & LYMBERAKIS, P. 2017. Status and diet of the European Shag (Mediterranean subspecies) Phalacrocorax aristotelis desmarestii in the Libyan Sea (south Crete) during the breeding season. Marine Ornithology 45: 1–9. During 2010–2012 we collected data on the population status and ecology of the European Shag (Mediterranean subspecies) Phalacrocorax aristotelis desmarestii on Gavdos Island (south Crete), conducting boat-based surveys, nest monitoring, and diet analysis. The species’ population was estimated at 80–110 pairs, with 59% breeding success and 1.6 fledglings per successful nest. Pellet morphological and genetic analysis of otoliths and fish bones, respectively, showed that the shags’ diet consisted of 31 species. A total of 4 223 otoliths were identified to species level; 47.2% belonged to sand smelts Atherina boyeri, 14.2% to bogues Boops boops, 11.3% to picarels Spicara smaris, and 10.5% to damselfishes Chromis chromis. -
Multi-Character Taxonomic Review, Systematics, and Biogeography of the Black- Capped/Tawny-Bellied Screech Owl (Megascops Atricapilla-M
Zootaxa 4949 (3): 401–444 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2021 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4949.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:2CAB47C9-2109-45DA-8F02-50D74D593DF2 Multi-character taxonomic review, systematics, and biogeography of the Black- capped/Tawny-bellied Screech Owl (Megascops atricapilla-M. watsonii) complex (Aves: Strigidae) SIDNEI M. DANTAS1,2, JASON D. WECKSTEIN3,4, JOHN BATES5, JOICIANE N. OLIVEIRA2,6, THERESE A. CATANACH4 & ALEXANDRE ALEIXO2,7* 1Zoology Graduate Program, Universidade Federal do Pará/Museu Paraense Emilio Goeldi, Belém-PA, Brazil. [email protected]; https://orcid.org/0000-0002-2281-0819 2Department of Zoology, Museu Paraense Emílio Goeldi, Belém-PA, Brazil. 3Department of Ornithology, Academy of Natural Sciences of Drexel University, 1900 Benjamin Franklin Parkway, Philadelphia, PA, USA 19096. [email protected]; https://orcid.org/0000-0003-3850-1196 4Department of Biodiversity, Earth and Environmental Science, Drexel University, 1900 Benjamin Franklin Parkway, Philadelphia, PA, USA 19096. [email protected]; https://orcid.org/0000-0001-7941-5724 5Negaunee Integrative Research Center, Field Museum of Natural History, 1400 S Lake Shore Drive Chicago, IL, USA 60605. [email protected]; https://orcid.org/0000-0002-5809-5941 6Graduate Program in Environmental Biology, Universidade Federal do Pará, Bragança-PA, Brazil. [email protected]; https://orcid.org/0000-0003-0496-7510 7Finnish Museum of Natural History, University of Helsinki, Helsinki, Finland. *Corresponding author. [email protected]; https://orcid.org/0000-0002-7816-9725 Abstract Megascops is the most species-rich owl genus in the New World, with 21 species currently recognized. -
Annotated Checklist of the Birds of Cuba
ANNOTATED CHECKLIST OF THE BIRDS OF CUBA Number 3 2020 Nils Navarro Pacheco www.EdicionesNuevosMundos.com 1 Senior Editor: Nils Navarro Pacheco Editors: Soledad Pagliuca, Kathleen Hennessey and Sharyn Thompson Cover Design: Scott Schiller Cover: Bee Hummingbird/Zunzuncito (Mellisuga helenae), Zapata Swamp, Matanzas, Cuba. Photo courtesy Aslam I. Castellón Maure Back cover Illustrations: Nils Navarro, © Endemic Birds of Cuba. A Comprehensive Field Guide, 2015 Published by Ediciones Nuevos Mundos www.EdicionesNuevosMundos.com [email protected] Annotated Checklist of the Birds of Cuba ©Nils Navarro Pacheco, 2020 ©Ediciones Nuevos Mundos, 2020 ISBN: 978-09909419-6-5 Recommended citation Navarro, N. 2020. Annotated Checklist of the Birds of Cuba. Ediciones Nuevos Mundos 3. 2 To the memory of Jim Wiley, a great friend, extraordinary person and scientist, a guiding light of Caribbean ornithology. He crossed many troubled waters in pursuit of expanding our knowledge of Cuban birds. 3 About the Author Nils Navarro Pacheco was born in Holguín, Cuba. by his own illustrations, creates a personalized He is a freelance naturalist, author and an field guide style that is both practical and useful, internationally acclaimed wildlife artist and with icons as substitutes for texts. It also includes scientific illustrator. A graduate of the Academy of other important features based on his personal Fine Arts with a major in painting, he served as experience and understanding of the needs of field curator of the herpetological collection of the guide users. Nils continues to contribute his Holguín Museum of Natural History, where he artwork and copyrights to BirdsCaribbean, other described several new species of lizards and frogs NGOs, and national and international institutions in for Cuba. -
(Tyto Alba) and Long-Eared Owl (Asio Otus) Mortality Along Motorways in Bourgogne-Champagne: Report and Suggestions
Barn Owl (Tyto alba) and Long-Eared Owl (Asio otus) Mortality Along Motorways in Bourgogne-Champagne: Report and Suggestions Hugues Baudvin1 The purpose of the study was to find where 305 km of motorways, from Dijon (Burgundy) and why two species of owls were killed by to Toul (Lorraine) and from Dijon to Saint- traffic along motorways. Three different factors Thibault (Champagne). Because of lack of have an important influence on the mortality of data, 46.1 km of road were not evaluated the two owl species: the biotops crossed by (discontinuous line figure 2). The distance motorways, the road elevation and the presence of small rodents, the Common Vole (Microtus arvalis) being most numerous. In order to limit the mortality caused by motorways, it is proposed to let the bordering vegetation grow naturally. Roadway-caused mortality of wildlife is a significant issue worldwide. Often, the impacts to wildlife occur along specific portions of roadways. Surveys along the roadways can identify these portions and identify the wildlife species being the most greatly impacted. Then, the management of roadside vegetation can help to reduce this negative impact. STUDY AREA AND METHODS The study area is located in the northeast of France, over the regions of Burgundy, Champagne, and Lorraine (fig. 1). It concerns Figure 2.—Owl mortality on motorways studied in northeastern France. studied is exactly 517.8 km (258.9 x 2 sides of the motorway). The study was conducted from November 1991 to December 1995. Dead animals were collected systematically along the motorway three times daily. The animals were placed in plastic bags and frozen for positive identification. -
Acoustic Location of Prey by Barn Owls {Tyto Alba) by Roger S
J. Exp. Biol. (1971), 54. S3S-573 535 With 5 plates and 5 text-figures Printed in Great Britain ACOUSTIC LOCATION OF PREY BY BARN OWLS {TYTO ALBA) BY ROGER S. PAYNE Rockefeller University and New York Zoological Society (Received 20 January 1970) INTRODUCTION The external ears of many species of owls are asymmetrical (Ridgeway, 1914; Stell- bogen, 1930). Although the asymmetry may involve the modification of different structures in different species (Stellbogen, 1930) the result is usually the same: one ear has its opening above the horizontal plane, the other below it. Though Pumphrey (1948), Southern (1955) and others have suggested that the asymmetrical ears of owls may be useful in hunting, prey location by hearing was first demonstrated by Payne & Drury (1958). Work prior to that time had suggested that, in the wild, light levels must often fall below that at which owls can see their prey, thus forcing them to rely upon some non-visual sense in hunting. Dice (1945) calculated the minimum intensi- ties of light required by the barn owl (Tyto alba), the long-eared owl (Asio otus), the barred owl (Strix varia), and the burrowing owl (Speotyto cunicularia) to see a dead mouse from a distance of 6 ft. His rough calculations of the reduction of light due to the absence of the moon, the shade of trees and shrubs, and various degrees of cloud cover led him to conclude that '.. .in the natural habitat of owls the intensity of illumination must often fall below the minimum at which the birds can see their prey'. -
Acta Ornithologica, 49 (2)
This is a peer-reviewed, post-print (final draft post-refereeing) version of the following published document and is licensed under All Rights Reserved license: Goodenough, Anne E ORCID: 0000-0002-7662-6670 (2014) Effects of Habitat on Breeding Success in a Declining Migrant Songbird: the Case of Pied Flycatcher Ficedula Hypoleuca. Acta Ornithologica, 49 (2). pp. 157-173. doi:10.3161/173484714X687046 Official URL: http://dx.doi.org/10.3161/173484714X687046 DOI: http://dx.doi.org/10.3161/173484714X687046 EPrint URI: http://eprints.glos.ac.uk/id/eprint/3356 Disclaimer The University of Gloucestershire has obtained warranties from all depositors as to their title in the material deposited and as to their right to deposit such material. The University of Gloucestershire makes no representation or warranties of commercial utility, title, or fitness for a particular purpose or any other warranty, express or implied in respect of any material deposited. The University of Gloucestershire makes no representation that the use of the materials will not infringe any patent, copyright, trademark or other property or proprietary rights. The University of Gloucestershire accepts no liability for any infringement of intellectual property rights in any material deposited but will remove such material from public view pending investigation in the event of an allegation of any such infringement. PLEASE SCROLL DOWN FOR TEXT. This is a peer-reviewed, post-print (final draft post-refereeing) version of the following published document: Goodenough, Anne E (2014). Effects of Habitat on Breeding Success in a Declining Migrant Songbird: the Case of Pied FlycatcherFicedula hypoleuca. Acta Ornithologica, 49 (2), 157-173. -
Short-Eared Owl (Asio Flammeus) Joseph Youngman Status: State Endangered
Short-eared Owl (Asio flammeus) Joseph Youngman Status: State Endangered Washtenaw Co., MI 12/21/2007 © Bruce Bowman (ClickHU to view a comparison of Atlas I to II) U Once seen flying low over open fields or During the MBBA I period, breeding was wetlands, the unique flight and appearance of confirmed in Chippewa County and probable the Short-eared Owl are not soon forgotten. One breeding was recorded in Isabella, Gratiot and of the most widespread owls in the world, its Lapeer. Between atlases there were midsummer North American breeding range extends from reports of Short-eared Owl from Osceola, northern Alaska and Canada south to California, Chippewa, Menominee (Whaley 1993), Huron Illinois, Indiana and Ohio. Individuals in the (Kielb 1996), Houghton (Byrne 2001), and northern part of its range are short to medium Benzie Counties (Byrne 2002) and confirmed distance migrants. It has been a rare breeder breeding records from Hillsdale County in 1996 and an uncommon migrant in Michigan. (Reinoehl 1997) and Monroe in 2000 (McWhirter 2001). The Monroe County record Distribution was a report of a Short-eared Owl nest with In a heavily forested state like Michigan, warm eggs on 15 February at Pt. Mouillee SGA, suitable breeding areas for the Short-eared Owl a very early nest date after an unusually warm are generally scarce. Extensive forest clearing winter. In Chippewa County throughout the state in the 1800s and early breeding/summering was noted in 2000 and 1900s may have provided some increased 2001 (Corace 2007) with an adult seen carrying breeding habitat, but more intensive modern food both years (Greg Corace pers. -
EARED OWL &Lpar;<I>ASIO OTUS</I>
j. RaptorRes. 31(2):175-186 ¸ 1997 The Raptor ResearchFoundation, Inc. THE LONG-EARED OWL (ASIO OTUS) AND FOREST MANAGEMENT: A REVIEW OF THE LITERATURE DENVER W. HOLT Owl ResearchInstitute, P.O. Box 8335, Missoula, MT 59807 U.S.A. ABSTRACT.--InNorth America, 13 of 20 breeding seasonstudies reporting on Long-earedOwl (Asio otus)reproduction were conductedin open country habitats,four in woodland or edge habitatsand three in predominantlywoodland habitat. Sixteenof 22 nonbreedingseason studies that reported com- munal roost siteswere located in forest/edge habitats,five reported locationsin open spaceand one wasfound within forest habitat.There is currentlylittle data to indicate either a negativeor positive effect of forest-managementpractices on this species.Although there appearsto be someevidence of population declinesin specificgeographic areas, these impactshave been attributed to lossof riparian vegetation,conversion of foraging areasto agriculturalfields and reforestationof open habitats.The Long-eared Owl's ecomorphologyis suggestiveof a speciesthat inhabits open country.Additionally, its primary food is small mammals (e.g., microtine and heteromyid rodents) which inhabit open country. Shouldthe Long-earedOwl be considereda forestowl? Research data would suggestno; however,studies from extensive deciduous and coniferous woodlands are needed. KEYWORDS: Long-earedOwl; forestry; habitat;, diet;, ecomorphology; Asio otus. El bfiho (Asiootus) y administracitn forestal:un revisode la literatura RESUMEN.-•Ennorte amtrica, 13 de 20 estudiosde