Checklist of Alaska Birds 24Th Edition

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Checklist of Alaska Birds 24Th Edition CHECKLIST OF ALASKA BIRDS 24th edition—2018 As of 1 January 2018 the list of avian taxa known in Alaska included 521 naturally- occurring species in 67 families and 21 orders. Phylogenetic sequence, limits of orders, families, and genera and English and scientific names of species follow The Check-list of North American Birds (7th ed., American Ornithologists’ Union 1998) and supplements (through 2017). Founded on archived specimens, the Alaska checklist increasingly includes new species known in Alaska only from (archived) photos, videotapes, and/or audio recordings. An appended ‘unsubstantiated’ list comprises an additional 21 species —including two species pairs—attributed to Alaska without specimen or photo substantiation.
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  • Effects of Nestling Diet on Growth and Adult Size of Zebra Finches (Poephila Guttata )
    THE AUK A QUARTERLY JOURNAL OF ORNITHOLOGY VOL. 104 APRIL 1987 NO. 2 EFFECTS OF NESTLING DIET ON GROWTH AND ADULT SIZE OF ZEBRA FINCHES (POEPHILA GUTTATA ) PETER T. BOAG Departmentof Biology,Queen's University, Kingston, Ontario K7L 3N6, Canada Al•STRACT.--Manipulationof the diet of Zebra Finch (Poephilaguttata) nestlings in the laboratoryshowed that a low-quality diet reducedgrowth ratesof nine externalmorpholog- ical characters,while a high-quality diet increasedgrowth rates.The growth of plumage characterswas least affectedby diet, while growth ratesof tarsusand masswere most af- fected. The treatments also produced differencesin the adult size of experimental birds, differencesnot evident in either their parentsor their own offspring.Diet quality had the strongestimpact on adult massand tarsuslength, while plumage and beak measurements were less affected. Analysis using principal componentsand characterratios showed that the shapeof experimentalbirds was affectedby the experimentaldiets, but to a minor extent comparedwith changesin overall size. Significantshape changes involved ratiosbetween fast- and slow-growingcharacters. The ratios of charactersthat grow at similar, slow rates (e.g. beak shape) were not affected by the diets. Environmental sourcesof morphological variation should not be neglectedin studiesof phenotypicvariation in birds. Received5 June 1986, accepted30 October1986. MORPHOLOGICAL differences between indi- fitness, and weather was seen in the nonran- vidual birds are often assignedfunctional sig- dom survival of House Sparrows collected by nificance, whether those individuals are of dif- Hiram Bumpus following a winter storm ferent species,different sexes,or different-size (O'Donald 1973, Fleischer and Johnston 1982). members of the same sex (Hamilton 1961, Se- Recently, investigators have tried to dem- lander 1966,Clark 1979,James 1982).
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  • <I>Actitis Hypoleucos</I>
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  • Purple Sandpiper
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  • Birds of the East Texas Baptist University Campus with Birds Observed Off-Campus During BIOL3400 Field Course
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  • Biogeographical Profiles of Shorebird Migration in Midcontinental North America
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    Conservation Evidence (2006) 3, 79-80 www.ConservationEvidence.com The effectiveness of opening up rush patches on encouraging breeding common snipe Gallinago gallinago at Rogersceugh Farm, Campfield Marsh RSPB reserve, Cumbria, England Holton N. & Allcorn R.I. Royal Society for the Protection of Birds, The Lodge, Sandy, Bedfordshire SG19 2GL, UK SUMMARY An area of improved grassland was dominated by rushes Juncus spp. and purple moor-grass Molinia caerulea . In order to try and attract breeding common snipe Gallinago gallinago , the rush was cut in 2003 with tractor mounted mowers and then grazed. In addition, 18 small scrapes were dug and higher water levels were maintained. The number of snipe increased from one nesting pair in 2003 to 11 nesting pairs in both 2004 and 2005. BACKGROUND Throughout the UK, common snipe Gallinago gallinago are undergoing a large population decline of between 25-49% in both breeding population and range over the last 25 years. Snipe feed by probing for invertebrates deep in soft, damp soil using their long bills. They also require wet marshy grassland areas with tussocks of taller vegetation for nesting. ACTION Figure 1 . All the rush on the improved grassland was cut with tractor mounted mowers. Study site: Rogersceugh Farm in Cumbria, north-west England, is a traditionally managed farm incorporating approximately 60 ha of waist high rush Juncus spp. and purple moor- reclaimed peatland. The RSPB purchased the grass Molinia caerulea . A breeding wader farm in order to raise water levels on the survey was carried out in 2003 prior to the adjacent raised mire whilst at the same time purchase of the farm by the RSPB.
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  • 1 ID Euring Latin Binomial English Name Phenology Galliformes
    BIRDS OF METAURO RIVER: A GREAT ORNITHOLOGICAL DIVERSITY IN A SMALL ITALIAN URBANIZING BIOTOPE, REQUIRING GREATER PROTECTION 1 SUPPORTING INFORMATION / APPENDICE Check list of the birds of Metauro river (mouth and lower course / Fano, PU), up to September 2020. Lista completa delle specie ornitiche del fiume Metauro (foce e basso corso /Fano, PU), aggiornata ad Settembre 2020. (*) In the study area 1 breeding attempt know in 1985, but in particolar conditions (Pandolfi & Giacchini, 1985; Poggiani & Dionisi, 1988a, 1988b, 2019). ID Euring Latin binomial English name Phenology GALLIFORMES Phasianidae 1 03700 Coturnix coturnix Common Quail Mr, B 2 03940 Phasianus colchicus Common Pheasant SB (R) ANSERIFORMES Anatidae 3 01690 Branta ruficollis The Red-breasted Goose A-1 (2012) 4 01610 Anser anser Greylag Goose Mi, Wi 5 01570 Anser fabalis Tundra/Taiga Bean Goose Mi, Wi 6 01590 Anser albifrons Greater White-fronted Goose A – 4 (1986, february and march 2012, 2017) 7 01520 Cygnus olor Mute Swan Mi 8 01540 Cygnus cygnus Whooper Swan A-1 (1984) 9 01730 Tadorna tadorna Common Shelduck Mr, Wi 10 01910 Spatula querquedula Garganey Mr (*) 11 01940 Spatula clypeata Northern Shoveler Mr, Wi 12 01820 Mareca strepera Gadwall Mr, Wi 13 01790 Mareca penelope Eurasian Wigeon Mr, Wi 14 01860 Anas platyrhynchos Mallard SB, Mr, W (R) 15 01890 Anas acuta Northern Pintail Mi, Wi 16 01840 Anas crecca Eurasian Teal Mr, W 17 01960 Netta rufina Red-crested Pochard A-4 (1977, 1994, 1996, 1997) 18 01980 Aythya ferina Common Pochard Mr, W 19 02020 Aythya nyroca Ferruginous
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  • Migration Timing, Routes, and Connectivity of Eurasian Woodcock Wintering in Britain and Ireland
    Migration Timing, Routes, and Connectivity of Eurasian Woodcock Wintering in Britain and Ireland ANDREW N. HOODLESS,1 Game & Wildlife Conservation Trust, Burgate Manor, Fordingbridge, Hampshire SP6 1EF, UK CHRISTOPHER J. HEWARD, Game & Wildlife Conservation Trust, Burgate Manor, Fordingbridge, Hampshire SP6 1EF, UK ABSTRACT Migration represents a critical time in the annual cycle of Eurasian woodcock (Scolopax rusticola), with poten- tial consequences for individual fitness and survival. In October–December, Eurasian woodcock migrate from breeding grounds in northern Eurasia over thousands of kilometres to western Europe, returning in March–May. The species is widely hunted in Europe, with 2.3–3.5 million individuals shot per year; hence, an understanding of the timing of migra- tion and routes taken is an essential part of developing sustainable flyway management. Our aims were to determine the timing and migration routes of Eurasian woodcock wintering in Britain and Ireland, and to assess the degree of connec- tivity between breeding and wintering sites. We present data from 52 Eurasian woodcock fitted with satellite tags in late winter 2012–2016, which indicate that the timing of spring departure varied annually and was positively correlated with temperature, with a mean departure date of 26 March (± 1.4 days SE). Spring migration distances averaged 2,851 ± 165 km (SE), with individuals typically making 5 stopovers. The majority of our sample of tagged Eurasian woodcock migrated to breeding sites in northwestern Russia (54%), with smaller proportions breeding in Denmark, Scandinavia, and Finland (29%); Poland, Latvia, and Belarus (9.5%); and central Russia (7.5%). The accumulated migration routes of tagged individ- uals suggest a main flyway for Eurasian woodcock wintering in Britain and Ireland through Belgium, the Netherlands, and Germany, and then dividing to pass through the countries immediately north and south of the Baltic Sea.
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  • 202 Common Redshank Put Your Logo Here
    Javier Blasco-Zumeta & Gerd-Michael Heinze Sponsor is needed. Write your name here Put your logo here 202 Common Redshank Ruff Redshank. Spring. Adult (02-V) COMMON REDSHANK (Tringa totanus ) SEXING IDENTIFICATION Plumage of both sexes alike. 27-28 cm. In spring with brownish upperparts barred dark; white rump; white tail with dark bars; wings with a broad white band on the ed- AGEING ge; white underparts with dark streaks on head, This species is a scarce breeder in Aragon, so neck and breast; red bill with dark tip; orange- only 3 age classes can be recognized: red legs. In autumn with darker colours on up- 1st year autumn with fresh plumage; median perparts: grey tinge on breast. coverts spotted pale on edge; tertials brown with buff and dark marks; pointed tail feathers; breast slightly streaked; dull reddish base of bill; yellowish legs. 2nd year spring similar to adult ; this age can be recognized only in birds with some unmoul- ted median wing coverts and/or tertials; flight feathers moderately worn. Adult with median coverts with whitish edge and dark subterminal band; tertials grey brown with variable markings: either plain or with dark sepia bars, sometimes with extensive dark markings; rounded tail feathers; underparts with variable amount of dark barring and spot- ting; reddish legs and base of bill. Redshank . Pattern of wing, tail and bill. SIMILAR SPECIES Recalls a Spotted Redhsank in autumn , without a white patch on wings and has a longer bill; Redshank. Ruff has a narrower wing band and two whi- Ageing. te bands on sides of uppertail Pattern of bill: top adult; bot- Spotted tom 1st Redshank.
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  • THE FAMILY ANATIDAE 43 Ernst Map
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  • 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.
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