CS-Normal-Haematological-Owl-1

Total Page:16

File Type:pdf, Size:1020Kb

CS-Normal-Haematological-Owl-1 Contributing Authors: Mélanie Ammersbach1 DVM | Hugues Beaufrère2 DVM, PhD, ABVP (Avian), ECZM (Avian) Annick Gionet Rollick3 BSc | Brent Hoff1 DVM, DVSc, Dip Tox 1 Department of Pathobiology and Animal Health Laboratory, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada 2 Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, Louisiana, U.S.A 3 The Owl Foundation, Vineland Station, Ontario, Canada contributing author contributing wls are represented throughout 6 of the 7 wildlife veterinarians and rehabilitators. Furthermore, continents, with 205 species split into two a great number of owl species are kept in captivity in distinct families; Tytonidae (16 species) and zoological institutions and for education programs. Strigidae (189 species). They range in size from Othe smallest, the Elf Owl at just 16 cm (40g) to the largest, the Eurasian Eagle Owl at 71 cm (4800g). As top predators they are useful as bio-indicators to evaluate ecosystem health. The International Union for Conservation of Nature and Natural Resources states 31% (based on 186 species) of those listed are categorized as a species of concern in need of protection and continued study and evaluation. With the exponentially decreasing natural world, owls are finding themselves ever closer to human habitation. Some species have managed to co-exist in the urban sprawl while others struggle to grab hold of a niche, often falling ill from S injury, starvation and competition for space. The rapidity of change in their environment makes adaptation a challenge. A thorough health check including a Some of the species included in the physical examination by the staff of the Owl study were small and so the blood For some species of owls, their only chance for a stable Foundation and Avian Veterinarian Hugues volume was small like in this ~ 80g population is through captive breeding and re-introduction Beaufrere was performed on the captive or Northern Saw-whet Owl (Aegolius pre-released owls to ensure that they are acadicus). Luckily, only 2 drops are programs. For others, a second chance to propagate in the healthy prior to sampling. needed to perform a full biochemistry wild through rehabilitation brings them into the hands of using the VetScan. Volume 52 | Vetcom | 23 norMal heMatologic p araMeterS on eleven SpecieS of OwlS While hematologic and biochemical information exist All owls were fasted for a minimum of 12 hours prior to for birds of prey, they are mainly available for diurnal sampling to prevent lipemia and post-prandial elevations raptors of the falconiformes (falcons) and accipitriformes in uric acid. The plasma was separated within 4 hours after (hawks, eagles) orders. However, there is currently a lack of blood collection to prevent changes in glucose, lactate hematological reference data in owls to assist in the treatment dehydrogenase and electrolytes in vitro. The samples were of illness or injury and for use in preventative medicine frozen at -20ºC until the biochemistry analysis using the practices to monitor owls placed in captivity. Strigiformes Avian/Reptilian Profile Plus rotors in a Vetscan VS2. Blood are not related to other birds of prey and have completely biochemistries were also performed on the Cobas 501 to different lifestyle and some physiological peculiarities. Thus perform an agreement analysis with the VS2, and a manual group-specific reference intervals are needed to increase the complete blood count was performed using 3 different value of blood test and their interpretation. techniques (Phloxine stain, Natt and Harrick solution, and estimation from the smear) to obtain the total leukocyte count. We are very grateful to Abaxis for donating Avian/Reptilian profile rotors for this project and the Animal Health Laboratory for allowing us to use their VS2 and Cobas 501. We hope that the results of this study will help improve the health and medical care of owls kept in captivity in rehabilitation centers and zoological institutions. We would also like to thank The Owl Foundation, The Mountsberg Conservation Center, The Toronto Wildlife Center and The Toronto Zoo and their staff for assisting us with blood collection from their healthy captive or pre-release owls. Blood sampling from the left jugular vein The fat distribution pattern and weight of of a Snowy Owl (Bubo scandiacus). (head the birds are monitored as part of the health down, facing to the left) check. The Vetscan Avian/Reptile profile provides a unique opportunity to perform a full plasma biochemical panel on S a small blood volume. The Vetscan is also easy to use and is a common benchtop laboratory analyzer in rehabilitation and zoological settings. In order to determine biochemical reference values in owl species, Abaxis donated rotors to a joint scientific project between the University of Guelph and Louisiana State University on strigiformes hematology. Blood samples were collected on close to 120 healthy releasable or captive owls from different centers, primarily from The Owl Foundation but also from the Mountsberg Conservation Area, the Toronto Wildlife Center and the Toronto Zoo. The species enrolled included European eagle owls (Bubo bubo), barred owls (Strix varia), great horned owl (Bubo virginianus), barn owl (Tyto alba), great gray owl (Strix laponica), eastern screech owl (Megascops asio), snowy owl (Bubo scandiacus), short-eared owl Asio flammeus Aegolius acadicus contributing author contributing ( ), saw-whet owl ( ), long- eared owl (Asio otus), and Northern hawk owl (Surnia ulula). The study is ongoing and more birds will continue to be recruited. Our goal is to collect a minimum of 20 individuals per species so that species-specific reference intervals can be established and compared with one another. Great Horned Owl (Bubo virginianus) 24 | Vetcom | Volume 52 norMal heMatologic p araMeterS on eleven SpecieS of OwlS Snowy Owl (Bubo scandiacus) Snowy Owl (Bubo scandiacus) Two Great Grey Owls Preliminary reference intervals for the Vetscan plasma biochemistry profile in the order strigiformes (SI units). Calculated using a non-parametric method. N, sample size; RI, reference interval. Values are reported with the measurement precision of the Vetscan. N Median RI Ca (mmol/L) 100 2.29 1.32-2.85 Phos (mmol/L) 100 1.11 0.34-2.23 Na (mmol/L) 99 151 138-165 K (mmol/L) 100 4.4 1.7-6.6 TP (mmol/L) 100 38 30-48 Albumin (g/L) 100 31 21-47 Globulin (g/L) 100 5 0-22 Glucose (mmol/L) 100 18.7 11.7-25.1 author contributing AST (IU/L) 100 207 104-410 CK (IU/L) 98 249 0-3169 Uric acid (µmol/L) 99 408 175-993 Bile acids (mmol/L) 99 <35 <35 Preliminary reference intervals for hematologic parameters in the order strigiformes. Calculated using a non-parametric method. N, sample size; RI, reference interval; PCV, packed cell volume; TS, total solids; RBC, red blood cell count; WBC, white blood cell count. NB/ RI are order-specific and not species-specific and are expected to be wider than species-specific RI. N Median RI PCV (%) 131 48.0 35.4-61.6 TS (g/L) 136 42.0 36-61 12 RBC (x 10 /L) 185 2.6 1.3-4.1 WBC (x 109/L) 159 11.5 2.1-28.3 S Heterophils (x 109/L) 159 4.3 0.6-15.6 Lymphocytes (x 109/L) 159 2.6 0.3-12.5 Monocytes (x 109/L) 159 0.9 0.1-4.3 Eosinophils (x 109/L) 159 1.2 0.1-6.3 Basophils (x 109/L) 159 0.2 0.0-1.2 Volume 52 | Vetcom | 25.
Recommended publications
  • Owl Eyes Activity
    EXPAND YOUR SENSES! TRY USING YOUR OWLTEX T EYES Age Range: Grades K-5 Time: 10-15 minutes Location: Indoor or outdoor space Materials: Yourself, a place to stand where you can focus your eyes on a fixed object at eye level. Instructional video: https://www.youtube.com/watch? Barn Owl v=2js74vxOXfg&feature=youtu.be Illustrations by Amira Maddison USING YOUR “OWL EYES” ACTIVATES YOUR PERIPHERAL VISION What is peripheral vision? It’s the ability to see movement and objects outside of what your eyes are directly focused on. ACTIVITY PART 1: BECOMING AN OWL Start by finding a quiet place to go and stand. Take a little bit of time to start imagining that you are becoming an owl. Notice where your feet are positioned. Make sure they are firmly positioned on the ground. Imagine that your feet have become talons and they are gripped around the branch of a tree. You are tucked away in the tree, so no one else can see you. Now it’s time to take it all in and comfortably stare into the distance. If you are outside, make sure you can see the sky and the ground. If you are inside, make sure you can see the ceiling and the floor. Notice your eyes going soft and imagine that you can now see everything happening around you. For a few minutes, take it all in. To finish, take a big breath in and when you breathe out, release that feeling of becoming an owl. Next, you will work on activating your eyesight.
    [Show full text]
  • Black-Flies and Leucocytozoon Spp. As Causes of Mortality in Juvenile Great Horned Owls in the Yukon, Canada
    Black-flies and Leucocytozoon spp. as Causes of Mortality in Juvenile Great Horned Owls in the Yukon, Canada D. Bruce Hunter1, Christoph Rohner2, and Doug C. Currie3 ABSTRACT.—Black fly feeding and infection with the blood parasite Leucocytozoon spp. caused mortality in juvenile Great Horned Owls (Bubo virginianus) in the Yukon, Canada during 1989-1990. The mortality occurred during a year of food shortage corresponding with the crash in snowshoe hare (Lepus americanus) populations. We postulate that the occurrence of disease was mediated by reduced food availability. Rohner (1994) evaluated the numerical re- black flies identified from Alaska, USA and the sponse of Great Horned Owls (Bubo virginianus) Yukon Territory, Canada, 36 percent are orni- to the snowshoe hare (Lepus americanus) cycle thophilic, 39 percent mammalophilic and 25 from 1988 to 1993 in the Kluane Lake area of percent autogenous (Currie 1997). Numerous southwestern Yukon, Canada. The survival of female black flies were obtained from the car- juvenile owls was very high during 1989 and casses of the juvenile owls, but only 45 of these 1990, both years of abundant hare populations. were sufficiently well preserved for identifica- Survival decreased in 1991, the first year of the tion. They belonged to four taxa as follows: snowshoe hare population decline (Rohner and Helodon (Distosimulium) pleuralis (Malloch), 1; Hunter 1996). Monitoring of nest sites Helodon (Parahelodon) decemarticulatus combined with tracking of individuals by radio- (Twinn), 3; Simulium (Eusimulium) aureum Fries telemetry provided us with carcasses of 28 ju- complex, 3; and Simulium (Eusimulium) venile owls found dead during 1990 and 1991 canonicolum (Dyar and Shannon) complex, 38 (Rohner and Doyle 1992).
    [Show full text]
  • A Multi-Gene Phylogeny of Aquiline Eagles (Aves: Accipitriformes) Reveals Extensive Paraphyly at the Genus Level
    Available online at www.sciencedirect.com MOLECULAR SCIENCE•NCE /W\/Q^DIRI DIRECT® PHYLOGENETICS AND EVOLUTION ELSEVIER Molecular Phylogenetics and Evolution 35 (2005) 147-164 www.elsevier.com/locate/ympev A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level Andreas J. Helbig'^*, Annett Kocum'^, Ingrid Seibold^, Michael J. Braun^ '^ Institute of Zoology, University of Greifswald, Vogelwarte Hiddensee, D-18565 Kloster, Germany Department of Zoology, National Museum of Natural History, Smithsonian Institution, 4210 Silver Hill Rd., Suitland, MD 20746, USA Received 19 March 2004; revised 21 September 2004 Available online 24 December 2004 Abstract The phylogeny of the tribe Aquilini (eagles with fully feathered tarsi) was investigated using 4.2 kb of DNA sequence of one mito- chondrial (cyt b) and three nuclear loci (RAG-1 coding region, LDH intron 3, and adenylate-kinase intron 5). Phylogenetic signal was highly congruent and complementary between mtDNA and nuclear genes. In addition to single-nucleotide variation, shared deletions in nuclear introns supported one basal and two peripheral clades within the Aquilini. Monophyly of the Aquilini relative to other birds of prey was confirmed. However, all polytypic genera within the tribe, Spizaetus, Aquila, Hieraaetus, turned out to be non-monophyletic. Old World Spizaetus and Stephanoaetus together appear to be the sister group of the rest of the Aquilini. Spiza- stur melanoleucus and Oroaetus isidori axe nested among the New World Spizaetus species and should be merged with that genus. The Old World 'Spizaetus' species should be assigned to the genus Nisaetus (Hodgson, 1836). The sister species of the two spotted eagles (Aquila clanga and Aquila pomarina) is the African Long-crested Eagle (Lophaetus occipitalis).
    [Show full text]
  • Tc & Forward & Owls-I-IX
    USDA Forest Service 1997 General Technical Report NC-190 Biology and Conservation of Owls of the Northern Hemisphere Second International Symposium February 5-9, 1997 Winnipeg, Manitoba, Canada Editors: James R. Duncan, Zoologist, Manitoba Conservation Data Centre Wildlife Branch, Manitoba Department of Natural Resources Box 24, 200 Saulteaux Crescent Winnipeg, MB CANADA R3J 3W3 <[email protected]> David H. Johnson, Wildlife Ecologist Washington Department of Fish and Wildlife 600 Capitol Way North Olympia, WA, USA 98501-1091 <[email protected]> Thomas H. Nicholls, retired formerly Project Leader and Research Plant Pathologist and Wildlife Biologist USDA Forest Service, North Central Forest Experiment Station 1992 Folwell Avenue St. Paul, MN, USA 55108-6148 <[email protected]> I 2nd Owl Symposium SPONSORS: (Listing of all symposium and publication sponsors, e.g., those donating $$) 1987 International Owl Symposium Fund; Jack Israel Schrieber Memorial Trust c/o Zoological Society of Manitoba; Lady Grayl Fund; Manitoba Hydro; Manitoba Natural Resources; Manitoba Naturalists Society; Manitoba Critical Wildlife Habitat Program; Metro Propane Ltd.; Pine Falls Paper Company; Raptor Research Foundation; Raptor Education Group, Inc.; Raptor Research Center of Boise State University, Boise, Idaho; Repap Manitoba; Canadian Wildlife Service, Environment Canada; USDI Bureau of Land Management; USDI Fish and Wildlife Service; USDA Forest Service, including the North Central Forest Experiment Station; Washington Department of Fish and Wildlife; The Wildlife Society - Washington Chapter; Wildlife Habitat Canada; Robert Bateman; Lawrence Blus; Nancy Claflin; Richard Clark; James Duncan; Bob Gehlert; Marge Gibson; Mary Houston; Stuart Houston; Edgar Jones; Katherine McKeever; Robert Nero; Glenn Proudfoot; Catherine Rich; Spencer Sealy; Mark Sobchuk; Tom Sproat; Peter Stacey; and Catherine Thexton.
    [Show full text]
  • Wallowa Wolverine Project: 2011‐2012 - April Progress Report
    Wallowa Wolverine Project: 2011‐2012 - April Progress Report Wallowa‐Whitman National Forest Field work began on 26 September 2011 and by the end of April 2012, we had established 26 camera stations in and adjacent to the Eagle Cap Wilderness in the Wallowa‐Whitman National Forest (Table 1). Access to camera sites was on foot, horse, snowmobile, ATV, skis, and snowshoes. The 6 camera stations that had wolverine visits in late winter 2011 were reestablished this season. Ten of the stations were below 6000’ elevation (4784’‐5820’). The remaining stations were located between 6014’ and 7373’ elevation. Additional stations may be added in May or June, depending on travel conditions in the mountains. One station was removed (WCAM1) because of its proximity to where the wolverine Stormy was trapped in December to prevent habituation of the wolverine to this site. Of the 26 established camera stations, 24 (92%) have been checked at least once (total=57 checks) and at these stations, there were 2,680 active camera days. One wolverine (Stormy; Fig.1‐3) has been photographed at 7 stations, including 4 stations where he was photographed in 2011. No other wolverines have been photographed to date. Eighteen other species have been detected at the camera stations (Table 2). Marten have been detected at 21 of the 24 (88%) stations that have been checked so far, and marten hair was collected at many of these stations and submitted for DNA analysis. We flew tracking flights on 6 days (Fig. 4), most in April, and have located wolverine tracks, or probable wolverine tracks, in 3 areas.
    [Show full text]
  • 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.
    [Show full text]
  • Arctic National Wildlife Refuge
    FACT SHEET Arctic National Wildlife Refuge ARCTIC BIRDS IN YOUR STATE The Arctic National Wildlife Refuge is a place unlike any Alabama - Ruby-crowned Kinglet Alaska - Redpoll other in the world. The Alaskan refuge, often referred to Arizona - Fox Sparrow as “America’s Serengeti,” is a remote sanctuary for diverse Arkansas - Mallard California - Snow Goose populations of migratory birds, fish, mammals, and marine Colorado - Bohemian Waxwing Connecticut - Greater Scaup life. The Refuge spans an area roughly the size of South Delaware - Black-bellied Plover Carolina and boasts snow-capped mountains, arctic tundra, Florida - Peregrine Falcon Georgia - Gray-checked Thrush foothills, wetlands, boreal forest, and fragile coastal plains. Hawaii - Wandering Tattler America’s Arctic Refuge was set aside as a safe haven for Idaho - Short-eared Owl Illinois - Northern Flicker wildlife in 1960, and it has remained wild in its more than Indiana - Dark-eyed Junco 50 years as a Refuge. Iowa - Sharp-shinned Hawk Kansas - Smith’s Longspur Kentucky – Merlin AMERICA’S LAST GREAT WILDERNESS Louisiana - Long-billed Dowitcher Maine - Least Sandpiper Maryland - Tundra Swan The Arctic Refuge is often mischaracterized as a blank, frozen void Massachusetts - Golden Plover of uninhabited tundra. Although winter frequently coats the Arc- Michigan - Long-tail Duck tic with snow and freezes the ground, it gives way to lush, vibrant Minnesota - Snowy Owl Mississippi – Northern Waterthrush growth in warmer months. In fact, the Refuge’s unparalleled diver- Missouri - American Pipit sity makes it the most biologically productive habitat in the North. Montana - Golden Eagle Nebraska - Wilson’s Warbler Landscape Nevada - Green-winged Teal The majestic Brooks Range rises 9,000 feet, providing sharp contrast New Hampshire - Dunlin New Jersey – Canvasback to the flat, wetlands-rich coastal plains at its feet.
    [Show full text]
  • Birds of Prey (Accipitriformes and Falconiformes) of Serra De Itabaiana National Park, Northeastern Brazil
    Acta Brasiliensis 4(3): 156-160, 2020 Original Article http://revistas.ufcg.edu.br/ActaBra http://dx.doi.org/10.22571/2526-4338416 Birds of prey (Accipitriformes and Falconiformes) of Serra de Itabaiana National Park, Northeastern Brazil Cleverton da Silvaa* i , Cristiano Schetini de Azevedob i , Juan Ruiz-Esparzac i , Adauto de Souza d i Ribeiro h a Programa de Pós-Graduação em Desenvolvimento e Meio Ambiente, Universidade Federal de Sergipe, Aracajú, São Cristóvão, 49100-100, Sergipe, Brasil. *[email protected] b Programa de Pós-Graduação em Ecologia de Biomas Tropicais, Universidade Federal de Ouro Preto, Ouro Preto, 35400-000, Minas Gerais, Brasil. c Universidade Federal de Sergipe, Nossa Senhora da Glória, 49680-000, Sergipe, Brasil. d Universidade Federal de Sergipe, Aracajú, São Cristóvão, 49100-100, Sergipe, Brasil. Received: June 20, 2020 / Accepted: August 27, 2020/ Published online: September 28, 2020 Abstract Birds of prey are important for maintaining ecosystems, since they can regulate the populations of vertebrates and invertebrates. However, anthropic activities, like habitat fragmentation, have been decreasing the number of birds of prey, affecting the habitat ecological relations and, decreasing biodiversity. Our objective was to evaluate species of birds of prey (Accipitriformes and Falconiformes) in a protected area of the Atlantic forest in northeastern Brazil. The area was sampled for 17 months using fixed points and walking along a pre-existing trail. Birds of prey were classified by their Punctual Abundance Index, threat status and forest dependence. Sixteen birds of prey were recorded, being the most common Rupornis magnirostris and Caracara plancus. Most species were considered rare in the area and not dependent of forest vegetation.
    [Show full text]
  • 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.
    [Show full text]
  • Bird) Species List
    Aves (Bird) Species List Higher Classification1 Kingdom: Animalia, Phyllum: Chordata, Class: Reptilia, Diapsida, Archosauria, Aves Order (O:) and Family (F:) English Name2 Scientific Name3 O: Tinamiformes (Tinamous) F: Tinamidae (Tinamous) Great Tinamou Tinamus major Highland Tinamou Nothocercus bonapartei O: Galliformes (Turkeys, Pheasants & Quail) F: Cracidae Black Guan Chamaepetes unicolor (Chachalacas, Guans & Curassows) Gray-headed Chachalaca Ortalis cinereiceps F: Odontophoridae (New World Quail) Black-breasted Wood-quail Odontophorus leucolaemus Buffy-crowned Wood-Partridge Dendrortyx leucophrys Marbled Wood-Quail Odontophorus gujanensis Spotted Wood-Quail Odontophorus guttatus O: Suliformes (Cormorants) F: Fregatidae (Frigatebirds) Magnificent Frigatebird Fregata magnificens O: Pelecaniformes (Pelicans, Tropicbirds & Allies) F: Ardeidae (Herons, Egrets & Bitterns) Cattle Egret Bubulcus ibis O: Charadriiformes (Sandpipers & Allies) F: Scolopacidae (Sandpipers) Spotted Sandpiper Actitis macularius O: Gruiformes (Cranes & Allies) F: Rallidae (Rails) Gray-Cowled Wood-Rail Aramides cajaneus O: Accipitriformes (Diurnal Birds of Prey) F: Cathartidae (Vultures & Condors) Black Vulture Coragyps atratus Turkey Vulture Cathartes aura F: Pandionidae (Osprey) Osprey Pandion haliaetus F: Accipitridae (Hawks, Eagles & Kites) Barred Hawk Morphnarchus princeps Broad-winged Hawk Buteo platypterus Double-toothed Kite Harpagus bidentatus Gray-headed Kite Leptodon cayanensis Northern Harrier Circus cyaneus Ornate Hawk-Eagle Spizaetus ornatus Red-tailed
    [Show full text]
  • Northern Saw-Whet Owls: Influence of Environmental Factors on Autumn Migration Dynamics
    Running head: NORTHERN SAW-WHET OWLS 1 Northern Saw-whet Owls: Influence of Environmental Factors on Autumn Migration Dynamics Hannah Murphy A Senior Thesis submitted in partial fulfillment of the requirements for graduation in the Honors Program Liberty University Fall 2016 NORTHERN SAW-WHET OWLS 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. ______________________________ Gene Sattler, Ph.D. Thesis Chair ______________________________ Timothy Brophy, Ph.D. Committee Member ______________________________ Edward Martin, Ph.D. Committee Member ______________________________ Brenda Ayres, Ph.D. Honors Director ______________________________ Date NORTHERN SAW-WHET OWLS 3 Abstract A portion of the population of the Northern Saw-whet Owl (Aegolius acadicus) leaves its breeding range in Canada and the northern United States each fall to winter where lesser snow cover allows easier access to prey. Study of its migratory dynamics is difficult, however, both because of its nocturnal habits and because it does not vocalize readily off of its breeding territory. Since 2002 banding studies in the Lynchburg area have investigated the migration dynamics of this species in central Virginia. However, few studies have examined the influence of environmental factors on capture rates of saw- whets during migration. Data were analyzed for the falls of 2007 and 2012, which were the two years of greatest migration volume in central Virginia, being “irruption years” in this species’ migratory cycle. In both years, nightly owl capture rates were strongly correlated with prevailing wind direction, with highest capture rates occurring during nights in which winds were predominantly out of the northeast quadrant.
    [Show full text]
  • Eastern Screech-Owl (Otus Asio)
    Wild Things in Your Woodlands Eastern Screech-Owl (Otus asio) The Eastern Screech-Owl is a small, nocturnal, predatory bird, about 8.5 inches in size. The robin-sized owl has short, rounded wings, bright yellow eyes, and a rounded head with visible “ear tufts.” The ear tufts, which the bird raises when alarmed, are otherwise inconspicuous. The facial disc is lightly mottled and has a prominent dark rim along the sides. The tail and the flight feathers of the wings are barred. The eastern screech-owl occurs in two color morphs, red and gray. The red color morph is more common near the coast, and the grey color morph is more common in the interior of the state. Male and female screech owls look alike. In the fall, light and temperature conditions mimic those of spring, and birds and amphibians sometimes begin calling again, a behavior called autumnal recrudescence. At this time, the screech owl’s tremulous call can be heard in a variety of habitats including open woodlands, deciduous forests, parks, farms, riparian areas, swamps, old orchards, small woodlots, and suburban areas. This small owl is an often common, nocturnal bird in much of New York State, though it is uncommon in heavily forested regions, at high elevations, and on Long Island. The screech owl is a year-round resident, spending both the breeding and non-breeding seasons in the same area. The screech owl nests in natural hollows or cavities in trees, old woodpecker holes, nesting boxes, and occasionally crevices in the sides of buildings. Screech owl pairs may roost together in the same tree cavity during the day throughout the breeding season.
    [Show full text]