Nomenclature of the Higher Groups in Swifts
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Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
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 -
Table of Contents 1 Experimental Design: Species Presented
SUPPLEMENTARY MATERIAL Table of contents 1 Experimental design: species presented.............................................................................................. 2 2 Information for the song and audio recordings used in the survey ................................................... 10 3 Statistical analyses and model fits .................................................................................................... 17 3.1 Disservices: mixed-effects model ............................................................................................. 17 3.2 Education: mixed-effects model ............................................................................................... 20 3.3 Birdwatching: mixed-effects model .......................................................................................... 23 3.4 Acoustic aesthetics: multinomial regression ............................................................................. 26 3.5 Identity: mixed-effects model ................................................................................................... 28 3.6 Bequest: logistic regression ...................................................................................................... 31 4 Results from the open-ended questions ............................................................................................ 34 4.1 Disservices ................................................................................................................................ 34 4.2 Birdwatching and acoustic -
Crustacea, Notostraca) from Iran
Journal of Biological Research -Thessaloniki 19 : 75 – 79 , 20 13 J. Biol. Res. -Thessalon. is available online at http://www.jbr.gr Indexed in: Wos (Web of science, IsI thomson), sCOPUs, CAs (Chemical Abstracts service) and dOAj (directory of Open Access journals) — Short CommuniCation — on the occurrence of Lepidurus apus (Linnaeus, 1758) (Crustacea, notostraca) from iran Behroz AtAshBAr 1,2 *, N aser Agh 2, L ynda BeLAdjAL 1 and johan MerteNs 1 1 Department of Biology , Faculty of Science , Ghent University , K.L. Ledeganckstraat 35 , 9000 Gent , Belgium 2 Department of Biology and Aquaculture , Artemia and Aquatic Animals Research Institute , Urmia University , Urmia-57153 , Iran received: 16 November 2011 Accepted after revision: 18 july 2012 the occurrence of Lepidurus apus in Iran is reported for the first time. this species was found in Aigher goli located in the mountains area, east Azerbaijan province (North east, Iran). details on biogeography, ecology and morphology of this species are provided. Key words: Lepidurus apus , Aigher goli, east Azerbaijan, Iran. INtrOdUCtION their world-wide distribution is due to their anti qu - ity, but possibly also to their passive transport: geo - Notostracan records date back to the Carboniferous graphical barriers are more effective for non-passive - and possibly up to the devonian period (Wallossek, ly distributed animals. From an ecological point of 1993, 1995; Kelber, 1998). In fact, there are Upper view, notostracans, like most branchiopods, are re - triassic Triops fossils from germany -
An Overview of Apus Apus-And Apus Apus Pekinensis Swifts Have Been Around for About 50 Million Years!
An overview of Apus apus-and Apus apus pekinensis Swifts have been around for about 50 million years! • Eocypselus rowei. • Found in Wyoming. • 12 centimetres from head to tail. • Around 50 million years old • Evolutionary precursor to swifts and hummingbirds. • Scaniacypselus fossil in Senckenberg Museum Frankfurt - Scanish Swift – 49 million years old. Photo Ulrich Tigges. • The story here is more about avian classification rather than details of swift evolution. • Reptiles to birds to modern birds! • Around 100 species of swift. Apus apus and Apus apus pekinensis Very widespread distribution Apus apus ‘HABITAT’ IS “AIR” • IT’S ALL ABOUT FLIGHT! • Look at the length of the wings- • Unlike most birds - e.g. sparrowhawk in woodland - IT’S NOT LIMITED BY SPECIFIC HABITAT REQUIREMENTS! • aerial plankton feeder • A bird of the air! • The Non Stop bird! Adapted at a molecular level. A powerful and finely tuned engine • 100% Type 1 muscle fibres – packed with mitochondria • Energy source is fat – more efficient than high octane fuel! • Same as Humming birds which are also Type 1 • Swifts like Jets refuel in mid air! Non Stop life in the air brings some unavoidable consequences! • Swallow can perch-passerine. • Feeds its fledged young – swift does not. • Builds its nest with mud. Swifts in cavity • Swallow preens when perched. • Can get Calcium and minerals from the ground. • Swallow roosts. Swift sleeps on wing. • Convergent evolution – species are not related. • Swift Torpor. Swallow not. • Totally different ball game. • Very different life strategies! • Researches need to be aware of this! • Many of the characteristics of the swift are the inevitable result of its evolutionary path. -
Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose -
Recent Bird Records from Fogo, Cape Verde Islands Rubén Baronea and Jens Heringb
Recent bird records from Fogo, Cape Verde Islands Rubén Baronea and Jens Heringb Observations récentes de Fogo, Îles du Cap-Vert. Des données sont présentées concernant 12 espèces d’oiseaux observées à Fogo, Îles du Cap-Vert, parmi lesquelles deux premières mentions pour l’île (Chevalier gambette Tringa totanus et Hirondelle de fenêtre Delichon urbicum), les premières données de nidification du Martinet du Cap-Vert Apus alexandri et les premières observations fiables du Phaéton à bec rouge Phaethon aethereus indiquant la nidification probable de celui-ci. Des informations sont également présentées sur d’autres taxons mal connus à Fogo, tels que certaines espèces pélagiques et l’Effraie des clochers Tyto alba detorta. Summary. We present data on 12 bird species observed on Fogo, Cape Verde Islands, among them two first records for the island (Common Redshank Tringa totanus and Common House Martin Delichon urbicum), the first breeding records of Cape Verde Swift Apus alexandri and the first reliable observations of Red-billed Tropicbird Phaethon aethereus indicating probable breeding. Information on other taxa poorly known on Fogo, such as some pelagic seabirds and Barn Owl Tyto alba detorta, is also given. ogo, one of the Cape Verde Islands, is situated reported previously, and some others for which F in the leeward group (‘Ilhas do Sotavento’), there are only a limited number of observations. c.724 km from the African continent. With Local information on breeding birds was mainly a surface area of 478 km2, the highest peak collected by RB. Dates of our visits are as follows: (Pico Novo) reaches 2,829 m (Michell-Thomé 18–21 October 2004 (JH & H. -
Triops (Apus), Str, Eptoce, Phalus and Estheria
ON POST-EMBRYONIC STAGES OF PHYLLOPOD CRUSTACEANS, TRIOPS (APUS), STR, EPTOCE, PHALUS AND ESTHERIA BY MRS. PREMLAXMI G. PAl (Department of Zoology, University of Pooita, Poona 7) Received January 4, 1957, after revision April 5, 1958 (Communicated by Dr. M. A. Moghe, F.A.SC.) CONTENTS PAGE INTRODUCTION .... 6 O t 229 MATERIAL AND METHODS .. O m m 230 OBSERVATIONS : (a) Triops .. • O .. 23t (b) Streptocephalus .. O • .. 236 (c) Estheria .. 6 D .. 240 DISCUSSION .... I Q .. 243 ACKNOWLEDGEMENTS • • O Q .. 248 SUMMARY .... • Q .. 248 REFERENCES .... I O .. 249 ABBREVIATIONS USED IN TEXT-FIGURES • • .. 250 INTRODUCTION CRUSTACEA, whose post-embryonic stages are described in this paper, viz., Triops (Apus) orientalis, Streptocephalus dichotomus Baird and Estheria are found in pools and shallow reservoirs on the table-lands of the Deccan Plateau and round about Poona. Most of these pools and ponds dry for some months during summer but the eggs of these remain in the soil. They hatch after the first showers of rain in early June. Larvm in various stages of development can be collected during June. Adults are available up to the end of January. The eggs of these animals are spherical and are provided with a hard coat which appears to be resistant to variations in external conditions. The 229 230 Mas. PREMLAXMI (~. PAt temperature of soil in Poona in summer varies from 94 ° F. to 124° F. (between 12 noon and 4p.m.). The occurrence of these phyllopods in Panchgani was noticed by several field workers. Cannon (1924) obtained a sample of dry soil containing eggs of Estheria, collected in the neighbourhood of Baghdad by Captain T. -
Nests of Lesser Swallow-Tailed Swift in Mexico
GENERALNOTES Nests of Lesser Swallow-tailed Swift in M&co.-Prior to Edwards ’ (1959. Auk. 76:358-359) discovery of an occupied nest on the trunk of a tree at Tikal, Guatemala, the Lesser Swallow-tailed Swift (Panyptila cayennensis), north of Honduras, was known only from a bird taken at Presidio, Veracruz, Mexico, in June, 1943 (Moore. 1947. Proc. Biol. Sot. Wash., 60:143-144). Edwards ’ note appeared shortly after I had submitted the following related observation made some 160 miles from Tikal, but in Mexico. These developments fulfill Moores’ expectation and suggest that the Veracruz specimen may not represent a disjunct population. On July 24, 1958, at Palenque Ruins, Chiapas, Mexico, elevation about 800 feet, I found a remarkable nest under the portico of the Temple of Inscriptions. From my sketch and notes made on the scene, I have been informed that it was a nest of P. cayennensis. The nest, about 18 inches long, was fastened on the corbeled wall some 12 feet above the floor. Only the upper one-third, about 6 inches in diameter, was attached. The remainder, consisting of slender entrance tubing, hung vertically free. Honey-colored and rough-textured, it seemed to be made entirely of long-tailed achenes that glistened. A torn place in the top, however, exposed numerous small feathers. This swift, known to nest in buildings, makes either a straight tube, or one with a bulbous top. The Palenque nest was of the latter type. Essentially, it fitted accounts given by Richmond (1898. Auk, 15:7-lo), Haverschmidt (1954. vi&on Bull., 66:6749; 1958. -
Gliding for a Free Lunch: Biomechanics of Foraging Flight in Common Swifts (Apus Apus) Tyson L
© 2018. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2018) 221, jeb186270. doi:10.1242/jeb.186270 RESEARCH ARTICLE Gliding for a free lunch: biomechanics of foraging flight in common swifts (Apus apus) Tyson L. Hedrick1,*,Cécile Pichot2 and Emmanuel de Margerie2,* ABSTRACT temporal (5–100 Hz) resolution, even for species where use of an Although the biomechanics of animal flight have been well studied in on-board satellite-based positioning package is currently infeasible laboratory apparatus such as wind tunnels for many years, the because of weight or other restrictions. Application of video applicability of these data to natural flight behaviour has been measurement methods has already revealed flight speeds well examined in few instances and mostly in the context of long-distance beyond those achieved in wind tunnels by quantifying mating or migration. Here, we used rotational stereo-videography to record the display behaviour in common swifts (Henningsson et al., 2010) and free-flight trajectories of foraging common swifts. We found that, hummingbirds (Clark, 2009), along with high-speed turns and despite their exquisite manoeuvring capabilities, the swifts only rarely pursuits in cliff swallows (Shelton et al., 2014). Field trajectory performed high-acceleration turns. More surprisingly, we also found recordings also revealed energy extraction from the ground to air that despite feeding on tiny insects probably moving with ambient wind speed gradient by foraging barn swallows (Warrick et al., flow, -
Breeds on Islands and Along Coasts of the Chukchi and Bering
FAMILY PTEROCLIDIDAE 217 Notes.--Also known as Common Puffin and, in Old World literature, as the Puffin. Fra- tercula arctica and F. corniculata constitutea superspecies(Mayr and Short 1970). Fratercula corniculata (Naumann). Horned Puffin. Mormon corniculata Naumann, 1821, Isis von Oken, col. 782. (Kamchatka.) Habitat.--Mostly pelagic;nests on rocky islandsin cliff crevicesand amongboulders, rarely in groundburrows. Distribution.--Breedson islandsand alongcoasts of the Chukchiand Bering seasfrom the DiomedeIslands and Cape Lisburnesouth to the AleutianIslands, and alongthe Pacific coast of western North America from the Alaska Peninsula and south-coastal Alaska south to British Columbia (QueenCharlotte Islands, and probablyelsewhere along the coast);and in Asia from northeasternSiberia (Kolyuchin Bay) southto the CommanderIslands, Kam- chatka,Sakhalin, and the northernKuril Islands.Nonbreeding birds occurin late springand summer south along the Pacific coast of North America to southernCalifornia, and north in Siberia to Wrangel and Herald islands. Winters from the Bering Sea and Aleutians south, at least casually,to the northwestern Hawaiian Islands (from Kure east to Laysan), and off North America (rarely) to southern California;and in Asia from northeasternSiberia southto Japan. Accidentalin Mackenzie (Basil Bay); a sight report for Baja California. Notes.--See comments under F. arctica. Fratercula cirrhata (Pallas). Tufted Puffin. Alca cirrhata Pallas, 1769, Spic. Zool. 1(5): 7, pl. i; pl. v, figs. 1-3. (in Mari inter Kamtschatcamet -
Pacific Swift: New to the Western Palearctic
British Birds VOLUME 83 NUMBER 2 FEBRUARY1990 Pacific Swift: new to the Western Palearctic Mike Parker n 19th June 1981, R. Waiden was on the deck of the Shell BT gas- Oplatform on the Leman Bank at 53°06'N 02°12'E, about 45 km off Happisburgh, Norfolk, when a bird attempted to land on his Shoulder. It then flew past him and clung to a wall on the rig. He caught the exhausted migrant at about 13.30 GMT, and sent it ashore on the next helicopter flight for release, as caring rig-workers often do. At 19.30 GMT, the helicopter arrived at Beccles Heliport in Suffolk, where I work. Mrs S. Irons rang me from the passenger terminal to say she had just been handed a swift which seemed unable to fly; knowing I was a birdwatcher, she asked if I could help. To my astonishment, the bird lying on her cardigan was indeed a swift, but with a startling white rump and all the [Brit. Sink 83: 43-46, February 1990] 43 44 Pacific Swift: new to the Western Palearctic Hi Pacific Swift Apus pacificus, Suffolk, June 1981 (Gary Davies) upper body feathers pale-tipped, giving a very scaly appearance. My colleagues were somewhat startled when I reacted by running around closing all the windows. At first, I assumed that it was one of the two European white-rumped species—Little Swift Apus qffinis or White-rumped Swift A. caffer. This bird, however, had an obvious forked tail, so I discounted Little Swift. I phoned C.