Wild Geese in Captivity by Bob Elgas Big Timber, Montana
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'Alae 'Ula (Hawaiian Moorhen)
NATIVE WATERBIRDS AVIAN NEWCOMERS These newly-created wetlands have been rapidly colonized by native waterbirds, Many non-native birds are attracted to the wetland restoration as well. The including four species that are highly endangered and found only in the Hawaiian long-necked white waders are Cattle Egrets, native to the Old World. Non-native Islands. The ‘Alae ‘Ula, or Hawaiian Moorhen (Gallinula chloropus sandvicensis), songbirds include the Common Myna, White-rumped Shama, two unrelated kinds of and Koloa Maoli, or Koloa Duck (Anas wyvilliana), have by now raised many broods cardinals, and three kinds of doves. Many of these exotic species probably became here, nesting among the native sedges. The Ae‘o, or Hawaiian Stilt (Himantopus established in recent decades as escaped cage birds. Before the accidental mexicanus knudseni), and the Nēnē, or Hawaiian Goose (Branta sandvicensis), stop introduction of mosquitoes in the 19th century and bird diseases they carry, by almost daily to rest and feed. In the morning and evening, watch for the ‘Auku‘u these coastal lowlands were home to native honeycreepers and other native or Black-crowned Night Heron (Nycticorax nycticorax). Long-distance migrants such songbirds, preserved abundantly in the fossil record of Makauwahi Cave. as the Kōlea or Pacific Golden Plover Pluvialis( fulva) stop to rest and often winter here, as part of their annual 10,000-mile migration from breeding grounds in the Arctic to wintering sites in the tropics. Bones of all these bird species occur as fossils in the sediment of adjacent Makauwahi Cave, showing that they have thrived here for thousands of years. -
Free Download! the Trumpeter Swan
G3647 The Trumpeter Swan by Sumner Matteson, Scott Craven and Donna Compton Snow-white Trumpeter Swans present a truly spectac- Swans of the Midwest ular sight. With a wingspan of more than 7 feet and a rumpeter Swans, along with ducks and geese, belong height of about 4 feet, the Trumpeter Swan (Cygnus buc- to the avian Order Anseriformes, Family Anatidae. cinator) ranks as the largest native waterfowl species in T Trumpeters have broad, flat bills with fine tooth-like North America. serrations along the edges which allow them to strain Because the Trumpeter Swan disappeared as a breed- aquatic plants and water. The birds’ long necks and ing bird in the Midwest, several states have launched strong feet allow them to uproot plants in water up to 4 restoration programs to reintroduce it to the region. This feet deep. publication will provide you with background informa- Most Trumpeter Swans weigh 21–30 pounds, tion on the Trumpeter Swan’s status and life history, and although some males exceed the average weight. The on restoration efforts being conducted in the upper male is called a cob; the female is called a pen; and a swan Midwest. in its first year is called a cygnet or juve- nile. The Trumpeter is often con- fused with the far more common Tundra Swan (formerly Whistling Swan, Cygnus columbianus), the only other native swan found routinely in North America. Tundra Swans can be seen in the upper Trumpeter Swan Midwest only during spring and fall migration. You can distinguish between the two native species most accurately by listening to their calls. -
THE ALEUTIAN CACKLING GOOSE in ARIZONA DAVID VANDER PLUYM, 2841 Mcculloch Blvd
THE ALEUTIAN CACKLING GOOSE IN ARIZONA DAVID VANDER PLUYM, 2841 McCulloch Blvd. N #1, Lake Havasu City, Arizona, 86403; [email protected] ABSTRACT: There is little published information about the occurrence of the Aleutian Cackling Goose (Branta hutchinsii leucopareia) in Arizona. Formerly listed as endangered by the U.S. Fish and Wildlife Service, this subspecies has rebounded, leading to an increase in numbers occurring outside its core range, including Arizona. Since the first in 1975, at least 24 well-founded records for Arizona have accumulated, one supported by a specimen, two by band recoveries, and 20 by diagnostic photo- graphs. Since 2013 the Aleutian Cackling Goose has occurred in Arizona annually between November and February. It is most frequent along the Colorado River, but records extend as far east as Willcox, Cochise County. The taxonomy of the “white-cheeked” geese is complex and debated. Currently, most treatments list 11 or 12 taxa in this group, and Banks et al. (2004) split them into two species: the Cackling Goose (Branta hutchinsii) and the Canada Goose (B. canadensis). Taxonomists generally recognize four extant subspecies of the Cackling Goose: hutchinsii, taverneri, minima, and leucopareia (Aleutian Cackling Goose). The now extinct population formerly breeding in the Commander and Kuril islands in Russia and wintering south to Japan has been considered a separate subspecies, asiatica (Banks et al. 2004), or a western population of leucopareia (e.g., Baldassarre 2014, Reeber 2015). Birds discovered breeding on the Semidi Islands in 1979 and wintering in coastal Oregon are phenotypically interme- diate between other populations of leucopareia and taverneri (Hatch and Hatch 1983) and do differ genetically from other populations of leucopareia, but they likely represent distinct populations of leucopareia rather than a valid separate taxon (Pierson et al. -
Cackling Geese in the East
Cackling Geese in the East Since 2004, when Cackling Geese were formally split from Canada Geese, birders have been keeping an eye out for small-bodied and short-billed geese, termed Cackling Geese, mixed in with “typical” large-bodied, wedge-headed Canada Geese. This ID challenge is very much like a birders version of “Where’s Waldo?”An excellent overview of this split was provided by OMNR waterfowl expert, Ken Abraham, in the winter of 2005. Here’s the link: http://www.ofo.ca/site/page/view/articles.cacklinggoose. I will attempt to make this discussion as clear, digestible, and casual as possible, but if anything is unclear, please email me at [email protected] and I would be happy to go over material. Below I provide an identification overview of “Richardson’s” (hutchinsii) Cackling Geese, Myth Busting, and Quiz photos. ______________________________________________________________________________ “Richardson’s” (hutchinsii) Cackling Geese Figure 1: Ontario’s Cackling Geese: an example of five “classic” hutchinsii Cackling Geese. Note the diminutive size overall; steep forehead; proportionally small head with “blocky” shape in most postures; peaked rear to crown; relatively thick and short bill (variable and may sometimes show a pronounced droop nearest the tip; lending to a Roman’s Nose look); show short and stubby neck (esp. in relaxed posture); small, compact body; pale emarginations often seen but not always; breast averages paler than Canada Geese but this is not the case on some birds, esp. juveniles. Andrew Haydon Park — 1 October 2013. Figure 2: More prototypical hutchinsii Cackling Geese, with three interior Canada Geese at back. -
Recent Introgression Between Taiga Bean Goose and Tundra Bean Goose Results in a Largely Homogeneous Landscape of Genetic Differentiation
Heredity (2020) 125:73–84 https://doi.org/10.1038/s41437-020-0322-z ARTICLE Recent introgression between Taiga Bean Goose and Tundra Bean Goose results in a largely homogeneous landscape of genetic differentiation 1 2 3 1 Jente Ottenburghs ● Johanna Honka ● Gerard J. D. M. Müskens ● Hans Ellegren Received: 12 December 2019 / Revised: 11 May 2020 / Accepted: 12 May 2020 / Published online: 26 May 2020 © The Author(s) 2020. This article is published with open access Abstract Several studies have uncovered a highly heterogeneous landscape of genetic differentiation across the genomes of closely related species. Specifically, genetic differentiation is often concentrated in particular genomic regions (“islands of differentiation”) that might contain barrier loci contributing to reproductive isolation, whereas the rest of the genome is homogenized by introgression. Alternatively, linked selection can produce differentiation islands in allopatry without introgression. We explored the influence of introgression on the landscape of genetic differentiation in two hybridizing goose taxa: the Taiga Bean Goose (Anser fabalis) and the Tundra Bean Goose (A. serrirostris). We re-sequenced the whole 1234567890();,: 1234567890();,: genomes of 18 individuals (9 of each taxon) and, using a combination of population genomic summary statistics and demographic modeling, we reconstructed the evolutionary history of these birds. Next, we quantified the impact of introgression on the build-up and maintenance of genetic differentiation. We found evidence for a scenario of allopatric divergence (about 2.5 million years ago) followed by recent secondary contact (about 60,000 years ago). Subsequent introgression events led to high levels of gene flow, mainly from the Tundra Bean Goose into the Taiga Bean Goose. -
Iucn Red Data List Information on Species Listed On, and Covered by Cms Appendices
UNEP/CMS/ScC-SC4/Doc.8/Rev.1/Annex 1 ANNEX 1 IUCN RED DATA LIST INFORMATION ON SPECIES LISTED ON, AND COVERED BY CMS APPENDICES Content General Information ................................................................................................................................................................................................................................ 2 Species in Appendix I ............................................................................................................................................................................................................................... 3 Mammalia ............................................................................................................................................................................................................................................ 4 Aves ...................................................................................................................................................................................................................................................... 7 Reptilia ............................................................................................................................................................................................................................................... 12 Pisces ................................................................................................................................................................................................................................................. -
Movements of Wild Ruddy Shelducks in the Central Asian Flyway and Their Spatial Relationship to Outbreaks of Highly Pathogenic Avian Influenza H5N1
Viruses 2013, 5, 2129-2152; doi:10.3390/v5092129 OPEN ACCESS viruses ISSN 1999-4915 www.mdpi.com/journal/viruses Article Movements of Wild Ruddy Shelducks in the Central Asian Flyway and Their Spatial Relationship to Outbreaks of Highly Pathogenic Avian Influenza H5N1 John Y. Takekawa 1,*, Diann J. Prosser 2, Bridget M. Collins 2, David C. Douglas 3, William M. Perry 4, Baoping Yan 5, Luo Ze 5, Yuansheng Hou 6, Fumin Lei 7, Tianxian Li 8, Yongdong Li 8 and Scott H. Newman 9,† 1 San Francisco Bay Estuary Field Station, Western Ecological Research Center, U.S. Geological Survey, 505 Azuar Drive, Vallejo, CA 94592, USA 2 Patuxent Wildlife Research Center, U.S. Geological Survey, Beltsville, MD 20705, USA; E-Mails: [email protected] (D.J.P.); [email protected] (B.M.C.) 3 Alaska Science Center, U.S. Geological Survey, Juneau, AK 99801, USA; E-Mail: [email protected] 4 Dixon Field Station, Western Ecological Research Center, U.S. Geological Survey, 800 Business Park Drive, Suite D, Dixon, CA 95620, USA; E-Mail: [email protected] 5 Computer Network Information Center (CNIC), Chinese Academy of Sciences, Beijing 100080, China; E-Mails: [email protected] (B.Y.); [email protected] (L.Z.) 6 Qinghai State Forestry Administration, Qinghai Lake National Nature Reserve (QLNNR), Xining 25700, Qinghai, China; E-Mail: [email protected] 7 Institute of Zoology (IOZ), Chinese Academy of Sciences, Beijing 100101, China; E-Mail: [email protected] 8 Institute of Virology (WIV), Chinese Academy of Sciences, Wuhan 430071, China; E-Mails: [email protected] (T.L.); [email protected] (Y.L.) 9 EMPRES Wildlife Health and Ecology Unit, Animal Health Service, Animal Production and Health Division, Food and Agriculture Organization of the United Nations, Rome 00153, Italy; E-Mail: [email protected] † Current address: Emergency Center for Transboundary Animal Diseases (ECTAD)-Vietnam, Food and Agriculture Organization of the United Nations (FAO), No. -
Ducks, Geese, and Swans of the World by Paul A
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 Ducks, Geese, and Swans of the World: Tribe Anserini (Swans and True Geese) 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., "Ducks, Geese, and Swans of the World: Tribe Anserini (Swans and True Geese)" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 5. https://digitalcommons.unl.edu/biosciducksgeeseswans/5 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. Tribe Anserini (Swans and True Geese) MAP 10. Breeding (hatching) and wintering (stippling) distributions of the mute swan, excluding introduced populations. Drawing on preceding page: Trumpeter Swan brownish feathers which diminish with age (except MuteSwan in the Polish swan, which has a white juvenile Cygnus alar (Cmelin) 1789 plumage), and the knob over the bill remains small through the second year of life. Other vernacular names. White swan, Polish swan; In the field, mute swans may be readily iden Hockerschwan (German); cygne muet (French); tified by their knobbed bill; their heavy neck, usu cisne mudo (Spanish). ally held in graceful curve; and their trait of swim ming with the inner wing feathers raised, especially Subspecies and range. -
4 East Dongting Lake P3-19
3 The functional use of East Dongting Lake, China, by wintering geese ANTHONY D. FOX1, CAO LEI2*, MARK BARTER3, EILEEN C. REES4, RICHARD D. HEARN4, CONG PEI HAO2, WANG XIN2, ZHANG YONG2, DOU SONG TAO2 & SHAO XU FANG2 1Department of Wildlife Ecology and Biodiversity, National Environmental Research Institute, University of Aarhus, Kalø, Grenåvej 14, DK-8410 Rønde, Denmark. 2School of Life Science, University of Science and Technology of China, Hefei, Anhui 230026, PR China. 321 Chivalry Avenue, Glen Waverley, Victoria 3150, Australia. 4Wildfowl and Wetlands Trust, Slimbridge, Gloucestershire GL2 7BT, UK. *Correspondence author. E-mail: [email protected] Abstract A survey and study of geese wintering at the East Dongting Lake National Nature Reserve, China, in February 2008 revealed internationally important numbers of Lesser White-fronted Geese Anser erythropus, Greater White-fronted Geese Anser albifrons and Bean Geese Anser fabilis using the site, as well as small numbers of Greylag Geese Anser anser. Only five Swan Geese Anser cygnoides were recorded, compared with several hundreds in the 1990s. Globally important numbers of Lesser White-fronted Geese spend the majority of daylight hours feeding on short grassland and sedge meadows within the core reserve areas of the National Nature Reserve, and also roost there at night. Greater White-fronted Geese were not studied in detail, but showed similar behaviour. Large numbers of Bean Geese of both serrirostris and middendorffi races showed differing feeding strategies. The small numbers of serrirostris tended to roost and feed in or near the reserve on short grassland, as did small proportions of middendorffi. However, the majority of middendorffi slept within the confines of the reserve by day and flew out at dusk, to nocturnal feeding areas at least 40 km north on the far side of the Yangtze River, returning 40–80 min after first light. -
"Bird of Mystery:" the Tule Greater White-Fronted Goose
Searching out a Central Valley "bird of mystery:" The Tule Greater White-fronted Goose John Y. Takekawa, U. S. Geological Survey, Western Ecological Research Center, San Francisco Bay Estuary Field Station, 505 Azuar Drive, Vallejo, CA 94592 "We lay frozen in the ditch for 30 minutes, peering cautiously through the cattails along the edge of the refuge road with binocu• lars to see into the next pond. The shallow water was filled with thousands of ducks, lesser snow geese, Ross' geese, and greater white-fronted geese, but we intently watched the small flock of 15• 20 geese swimming slowly at the edge of thepond, adjacent to a net hidden along the graveled road. These geese were larger-bodied and darker than the other greater white-fronted geese in the pond, with darker heads and larger bills. With the flip of a switch, the rockets roared to life, pulling the camouflaged nets over theflock. We scrambled up the bank and raced quickly to secure the net, for these were Tule Geese, the most uncommon subspecies of greater white-fronted geese in the world. " [From the author's field notes] GREATER WHITE-FRONTED GOOSE POPULAnONS Greater White-fronted Geese (Anser albifrons) are one of the few waterfowl species that breeds across the Arctic from Russia to Canada and Greenland. Four subspecies are currently recognized (Owen 1980), includ• ing the nominate European form (A. a. albifrons), The North American "Pacific White-fronted Goose" (A. a.frontalis), the Greenland race (A. a. flavirostris), and, the subject of this paper, the "Tule Goose" (A. a. -
Population Management of Anseriformes in AZA Keith Lovett
Population Management of Anseriformes in AZA Keith Lovett Executive Director of Buttonwood Park Zoo and Buttonwood Park Zoological Society Anseriformes Taxon Advisory Group Chair Waterfowl Diversity in AZA 135 SPECIES Waterfowl Declines in AZA Why the Decline? Loss of Knowledge Loss of Waterfowl Exhibits New Exhibit Design New Exhibit Design New Exhibit Design Cost Acquisition Quarantine Shipment Exams Cost Examples Acquisition: $250 Shipment by commercial airline: $150 Quarantine medical testing (CBC, Chem Profile, Fecal Culture): $300 (2 birds) Vet Care Labor: $500 (1 hr a day for 30 days plus exit exam) Total: $1200 Zoos and Private Aviculture How do we respond? Managed Programs List of SSP’s GREEN SSP – NONE YELLOW SSP – 10 RED SSP – 3 CANDIDATE PROGRAM - 2 Criteria Yellow SSP White-wing Wood Duck - 48.55.8 (111) at 13 institutions African Pygmy Goose - 50.45.3 (98) at 24 institutions Swan Goose – 36.31 (67) at 9 institutions Nene Goose - 37.35.4 (76) at 20 institutions Crested Screamer - 55.44.10 (109) at 49 institutions Coscoroba Swan – 18.17 (35) at 18 institutions Marbled Teal - 94.94.00 (188) at 40 institutions West Indian Whistling Duck - 38.26.2 (66) at 19 institutions Madagascar Teal 40.48.6 (94) at 15 institutions Orinoco Goose - 47.35.2 (84) at 21 institutions Red SSP Red-breasted Goose - 32.28.7 (67) at 17 institutions Spotted Whistling Duck - 18.9 (27) at 6 institutions Indian Pygmy Goose - 13.12.3 (28) at 11 institutions Candidate Program Species Baer’s Pochard - 29.25.1 (55) at 8 institutions -
2.10.1 Numbers and Distribution Greylag Goose Has a Complex Population Structure in Europe A
2.10 Greylag Goose ( Anser anser ) 2.10.1 Numbers and distribution Greylag Goose has a complex population structure in Europe and many countries have non-migratory populations which are joined by migrants on passage and in winter. Denmark, The Netherlands, Spain, the UK, Germany and Hungary hold large wintering populations. This is a numerous species in Central Asia and Iran, with important breeding and staging sites in Kazakhstan, and wintering sites in Uzbekistan, Turkmenistan and especially Iran. The highest counts of Greylag Geese have been made at sites in Russia and Kazakhstan (Table 2.9). 100,000 have been recorded staging at the Stepnoi State Refuge, and 50,000 at the Svir Delta in Russia, and 70,000 were counted at Sholack Lake, Kazakhstan in January 1995. Large numbers winter in Spain, where 43,521 at The Doñana National Park 1n 1995 and 39,296 at Lagunas de Vilafafila in 1999 are high recent count totals. Iran has more records of important concentrations of Greylag Geese than other countries with 48,100 at Fereydoon Kenar in 2003 by far the highest count, followed by 12,700 at Varamin Lake in 1997. In Northern Europe, 57,104 at Westerschelde and Saeftinge, The Netherlands in 1999, 22,710 at Filso Lake, Denmark in 1996 and 19,150 at Loch of Skene, Scotland in 1991 are typical high counts. In central and eastern Europe, 22,000 were counted at Fulupszallas Szikes To, Hungary, in 1995, and 21,822 at the Danube Delta, Romania in 1992. There are important winter concentrations in North Africa, where Lac Fetzara, Algeria, held 13,400 in January 1994.