The Status of the White-Headed Duck Oxyura Leucocephala
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Oxyura Jamaicensis Global Invasive
FULL ACCOUNT FOR: Oxyura jamaicensis Oxyura jamaicensis System: Freshwater_terrestrial Kingdom Phylum Class Order Family Animalia Chordata Aves Anseriformes Anatidae Common name northern ruddy duck (English), Amerikansk skarveand (Danish), stivhaleand (Norwegian), schwartzkopf ruderente (German), rosse stekelstaarteend (Dutch), Amerikansk kopparand (Swedish), ruddy duck (English), gobbo della giamaica (Italian), erismature rouse (French), malvasía cabeciblanca (Spanish), hrókönd (Icelandic) Synonym Anas jamaicensis , Gmelin 1789 Similar species Summary Oxyura jamaicensis (ruddy duck) is native to North America. It was imported into wildfowl collections in the UK in the 1940s and subsequently escaped to form a feral population from which birds are now spreading as far as Spain, where they threaten the globally endangered white-headed duck (Oxyura leucocephala) with extinction through introgressive hybridisation and competition. A regional trial of control measures, in which over 2,000 birds have been controlled, is ongoing in the UK. Control programmes are also in place in France, Spain and Portugal and are urgently needed in The Netherlands and Belgium. Oxyura jamaicensis are relatively easy to shoot as they tend not to leave water-bodies during control activities. view this species on IUCN Red List Species Description Oxyura jamaicensis (ruddy duck) is a small diving duck with a long tail, often held erect. On an average the females weigh 550g and males around 600g. During the breeding season males can be distinguished from other ducks by a white cheek patch, chestnut red body plumage, and blue bill. Females are distinguished by their body structure and off-white cheek split by a horizontal brown stripe. Both sexes can be distinguished from the white-headed duck by their smaller size, shorter tail, thinner cheek stripe and concave bill profile. -
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 -
A 2010 Supplement to Ducks, Geese, and Swans of the World
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 20. https://digitalcommons.unl.edu/biosciducksgeeseswans/20 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. The World’s Waterfowl in the 21st Century: A 200 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard Pages xvii–xxiii: recent taxonomic changes, I have revised sev- Introduction to the Family Anatidae eral of the range maps to conform with more current information. For these updates I have Since the 978 publication of my Ducks, Geese relied largely on Kear (2005). and Swans of the World hundreds if not thou- Other important waterfowl books published sands of publications on the Anatidae have since 978 and covering the entire waterfowl appeared, making a comprehensive literature family include an identification guide to the supplement and text updating impossible. -
Appendix, French Names, Supplement
685 APPENDIX Part 1. Speciesreported from the A.O.U. Check-list area with insufficient evidencefor placementon the main list. Specieson this list havebeen reported (published) as occurring in the geographicarea coveredby this Check-list.However, their occurrenceis considered hypotheticalfor one of more of the following reasons: 1. Physicalevidence for their presence(e.g., specimen,photograph, video-tape, audio- recording)is lacking,of disputedorigin, or unknown.See the Prefacefor furtherdiscussion. 2. The naturaloccurrence (unrestrained by humans)of the speciesis disputed. 3. An introducedpopulation has failed to becomeestablished. 4. Inclusionin previouseditions of the Check-listwas basedexclusively on recordsfrom Greenland, which is now outside the A.O.U. Check-list area. Phoebastria irrorata (Salvin). Waved Albatross. Diornedeairrorata Salvin, 1883, Proc. Zool. Soc. London, p. 430. (Callao Bay, Peru.) This speciesbreeds on Hood Island in the Galapagosand on Isla de la Plata off Ecuador, and rangesat seaalong the coastsof Ecuadorand Peru. A specimenwas takenjust outside the North American area at Octavia Rocks, Colombia, near the Panama-Colombiaboundary (8 March 1941, R. C. Murphy). There are sight reportsfrom Panama,west of Pitias Bay, Dari6n, 26 February1941 (Ridgely 1976), and southwestof the Pearl Islands,27 September 1964. Also known as GalapagosAlbatross. ThalassarchechrysosWma (Forster). Gray-headed Albatross. Diornedeachrysostorna J. R. Forster,1785, M6m. Math. Phys. Acad. Sci. Paris 10: 571, pl. 14. (voisinagedu cerclepolaire antarctique & dansl'Ocean Pacifique= Isla de los Estados[= StatenIsland], off Tierra del Fuego.) This speciesbreeds on islandsoff CapeHorn, in the SouthAtlantic, in the southernIndian Ocean,and off New Zealand.Reports from Oregon(mouth of the ColumbiaRiver), California (coastnear Golden Gate), and Panama(Bay of Chiriqu0 are unsatisfactory(see A.O.U. -
The Function and Evolution of the Supraorbital Process in Ducks
THE FUNCTION AND EVOLUTION OF THE SUPRAORBITAL PROCESS IN DUCKS ROBERTJ. RAIKOW THE anteriormargin of the orbit in ducksis formedby the lacrimalbone, which articulateswith the anterolateralmargin of the frontal boneand the posterodorsalcorner of the maxillary processof the nasal bone. The evolu- tion of this bone in birds generally has been dealt with recently by Cracraft (Amer. Midl. Naturalist, 80: 316, 1968), whoseterminology for the parts of the lacrimal bone is followedhere. In many ducksthe postero- dorsalcorner of the lacrimal is marked by a small tubercle,which serves as the site of attachment of the anterior end of the orbital membrane,a sheetof connectivetissue that coversand protectsthe dorsalaspect of the eyeball. In some forms this tubercle has become elongated to form a stout, finger-like projection, the supraorbitalprocess. This appears to provide mechanicalprotection to the eyeball and salt gland (Figure 1). Table 1 lists the occurrenceand degree of developmentof this process in the skulls of all living generaof ducks. CORRELATION WITH FEEDING AND LOCOMOTOR HABITS In the following discussion,data on feeding habits are from Delacour (The waterfowlof the world,vols. 1-3, London,Country Life Ltd., 1954, 1956, 1959). Table 1 showsthat the supraorbital processis developed significantlyonly in certain groupsof ducks that feed underwater. It is absentor rudimentaryin the Tadornini, Cairinini, and Anatini, which are primarily surfacefeeders, but also in Merganetta arma.ta,the Torrent Duck, which feedsunderwater. In the Aythyini it is fairly well-developed in severalspecies of Aythya, which are excellentdivers, but is rudimentary in Netta peposaca,which is moreof a surfacefeeder. It is alsorudimentary in the Canvasback,Aythya valisineria,which dives for vegetation.Among the Mergini the supraorbitalprocess is highly developedin eiders (Poly- sticta, Somateria) , scoters( M elanitta) , and Long-tailed Duck ( Clangula byemalls), all of which feed mainly on invertebratestaken from the bottom. -
Lista Das Aves Do Brasil
90 Annotated checklist of the birds of Brazil by the Brazilian Ornithological Records Committee / Lista comentada das aves do Brasil pelo Comitê Brasileiro de Registros Ornitológicos content / conteÚDO Abstract ............................. 91 Charadriiformes ......................121 Scleruridae .............187 Charadriidae .........121 Dendrocolaptidae ...188 Introduction ........................ 92 Haematopodidae ...121 Xenopidae .............. 195 Methods ................................ 92 Recurvirostridae ....122 Furnariidae ............. 195 Burhinidae ............122 Tyrannides .......................203 Results ................................... 94 Chionidae .............122 Pipridae ..................203 Scolopacidae .........122 Oxyruncidae ..........206 Discussion ............................. 94 Thinocoridae .........124 Onychorhynchidae 206 Checklist of birds of Brazil 96 Jacanidae ...............124 Tityridae ................207 Rheiformes .............................. 96 Rostratulidae .........124 Cotingidae .............209 Tinamiformes .......................... 96 Glareolidae ............124 Pipritidae ............... 211 Anseriformes ........................... 98 Stercorariidae ........125 Platyrinchidae......... 211 Anhimidae ............ 98 Laridae ..................125 Tachurisidae ...........212 Anatidae ................ 98 Sternidae ...............126 Rhynchocyclidae ....212 Galliformes ..............................100 Rynchopidae .........127 Tyrannidae ............. 218 Cracidae ................100 Columbiformes -
Phylogeny and Comparative Ecology of Stiff-Tailed Ducks (Anatidae: Oxyurini)
Wilson Bull., 107(2), 1995, pp. 214-234 PHYLOGENY AND COMPARATIVE ECOLOGY OF STIFF-TAILED DUCKS (ANATIDAE: OXYURINI) BRADLEY C. LIVEZEY’ ABSTRACT.-A cladistic analysis of the stiff-tailed ducks (Anatidae: Oxyurini) was con- ducted using 92 morphological characters. The analysis produced one minimum-length, completely dichotomous phylogenetic tree of high consistency (consistency index for infor- mative characters, 0.74). Monophyly of the tribe was supported by 17 unambiguous syna- pomorphies. Within the tribe, Heteronetta (1 species) is the sister-group of other members; within the latter clade (supported by 2 1 unambiguous synapomorphies), Nomonyx (1 species) is the sister-group of Oxyura (6 species) + Biziura (I species). The latter clade is supported by 10 unambiguous synapomorphies. Monophyly of Oxyuru proper is supported by three unambiguous synapomorphies. All branches in the shortest tree except that uniting Oxyuva, exclusive of jumaicensis, were conserved in a majority-rule consensus tree of 1000 boot- strapped replicates. Biziuru and (to a lesser extent) Heteronetta were highly autapomorphic. Modest evolutionary patterns in body mass, reproductive parameters, and sexual dimorphism are evident, with the most marked, correlated changes occurring in Heteronetta and (es- pecially) Biziura. The implications of these evolutionary trends for reproductive ecology and biogeographic patterns are discussed, and a phylogenetic classification of the tribe is presented. Received 27 April 1994, accepted 10 Nov. 1994. The stiff-tailed ducks (Anatidae: Oxyurini) include some of the most distinctive species of waterfowl; among its members are the only obligate nest-parasite (Black-headed Duck; Heteronetta atricapilla) and the spe- cies showing the greatest sexual size dimorphism (Musk Duck; Biziuru lob&z) in the order Anseriformes (Delacour 1959; Johnsgard 1962, 1978; Weller 1968; Livezey 1986). -
Diving Ducks Wildlife Note
Diving Ducks Pennsylvania ducks may be grouped into two types: diving ducks and dabbling or puddle ducks. Diving ducks often spend much more of their time farther out from shore than puddle ducks. Both groups can be found on streams, rivers, lakes and marshes. This note covers 15 species commonly called diving ducks. redhead Diving ducks eat seeds and other parts of aquatic plants, form monogamous pairs that last until the female begins fish, insects, mollusks, crustaceans and other invertebrates. incubating eggs; then, the male leaves the area and usually They dive underwater to obtain much of their food. They joins a band of other males. have large broad feet, fully webbed and with strongly lobed hind toes, that act as paddles. Their legs are spaced Nesting habits and habitats vary from species to species. widely apart and located well back on the body, improving Generally, female diving ducks lay 5 to 15 eggs in diving efficiency but limiting agility on land. Their bodies vegetation, tree cavities, or rock crevices over or near the are compact, and their wings have relatively small surface water. Because females do not start incubating a clutch areas; noticeably more narrow than puddle ducks. While until they lay their last egg, young develop simultaneously this arrangement helps their diving and swimming, it and all hatch at about the same time. hinders their ability to become airborne. Instead of Ducklings are covered with down, patterned with shades springing straight out of the water into flight, as puddle of yellow or brown to break up their body outlines. -
Waterfowl of North America: WHISTLING DUCKS Tribe Dendrocygnini
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Waterfowl of North America, Revised Edition (2010) Papers in the Biological Sciences 2010 Waterfowl of North America: WHISTLING DUCKS Tribe Dendrocygnini Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciwaterfowlna Part of the Ornithology Commons Johnsgard, Paul A., "Waterfowl of North America: WHISTLING DUCKS Tribe Dendrocygnini" (2010). Waterfowl of North America, Revised Edition (2010). 8. https://digitalcommons.unl.edu/biosciwaterfowlna/8 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Waterfowl of North America, Revised Edition (2010) by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. WHISTLING DUCKS Tribe Dendrocygnini Whistling ducks comprise a group of nine species that are primarily of tropical and subtropical distribution. In common with the swans and true geese (which with them comprise the subfamily Anserinae), the included spe cies have a reticulated tarsal surface pattern, lack sexual dimorphism in plum age, produce vocalizations that are similar or identical in both sexes, form relatively permanent pair bonds, and lack complex pair-forming behavior pat terns. Unlike the geese and swans, whistling ducks have clear, often melodious whistling voices that are the basis for their group name. The alternative name, tree ducks, is far less appropriate, since few of the species regularly perch or nest in trees. All the species have relatively long legs and large feet that extend beyond the fairly short tail when the birds are in flight. -
Life History Account for Ruddy Duck
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group RUDDY DUCK Oxyura jamaicensis Family: ANATIDAE Order: ANSERIFORMES Class: AVES B107 Written by: S. Granholm Reviewed by: D. Raveling Edited by: R. Duke DISTRIBUTION, ABUNDANCE, AND SEASONALITY A common to abundant yearlong resident throughout much of California, excluding the southern deserts and the Sierra Nevada. Prefers estuarine (bays, salt ponds) and lacustrine habitats, and occasionally found on marine waters near shore. Nests in fresh emergent wetland bordering lacustrine habitats. From late September to April, common to abundant along coast, on Salton Sea, and in northeastern California, and common elsewhere in California, except in the high Sierra Nevada. Numbers decline markedly in northeastern California in some winters. Fairly uncommon through summer, except locally common, especially in northeastern California, and rare along coast and in northern mountains. 75% of breeding population in California is in the Klamath Basin. Breeds only in freshwater habitats, even at the Salton Sea, where it nests in fresh emergent wetland at river mouths (Cogswell 1977, U.S. Fish and Wildlife Service 1978, 1979, McCaskie et al. 1979, Garrett and Dunn 1981). SPECIFIC HABITAT REQUIREMENTS Feeding: Major plant foods are seeds, tubers, foliage and stems of submerged aquatic plants; also algae and seeds of bulrush. Animal foods include aquatic insects in freshwater, and mollusks, crustaceans, and worms in saltwater. Eats mostly plant materials in winter (Palmer 1976), but mostly animal foods in some coastal areas, and in summer (Siegfried 1973, Barcelona 1976). Usually dives to bottom and gleans food, or filters bottom sediments; but also filters invertebrates from surface and subsurface water, or dips head in water to eat submerged plants. -
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 -
Landfill Contamination Problems: a General Perspective and Engineering Geology Aspects
Giornale di Geologia Applicata 1 (2005) 203 –211, doi: 10.1474/GGA.2005-01.0-20.0020 Landfill contamination problems: a general perspective and engineering geology aspects A. Tazioli & G. S. Tazioli Department of "Fisica e Ingegneria dei Materiali e del Territorio" Technical University of the Marches, Ancona, via Brecce Bianche. Italy ABSTRACT. Using isotopic methods for the investigation of leachate contamination has produced good results mainly for the control of the interference between landfill activity processes and the underground groundwater environment. In this paper the results of study performed in several italian landfill sites are presented. The results obtained from the investigated areas show that the knowledge of background values of the environment is basic for pollution purpose. In particular, Oxigen-18, Deuterium and Tritium values have allowed groundwater residence times and location of recharge areas to be identified. After that, the use of tritium as pollution tracer provides information on the presence of leachate contamination earlier and better than chemical changes of the standard pollution parameters. Deuterium and Oxygen-18 values of leachate always appear to be somewhat different with respect to the groundwater values, but they can be used as contamination index only in cases of high fractions of leachate. Key terms: Landfill, Monitoring, Tritium, Environmental isotopes, Leachate, Groundwater, Pollution, Rainwater, Waste, Recharge, Leakage, Aquifer, Chemistry. Introduction The qualitative and quantitative characteristics of the fluxes of leachate and biogas are related to the solid waste and to Groundwater and surface water contamination by sanitary the processes taking place in the landfill. An impact on the landfills has been monitored since 1989 in Italy by using underground environment is generally caused by exit- isotope techniques combined with chemical analyses.