Print This Article
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Disaggregation of Bird Families Listed on Cms Appendix Ii
Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2. -
Wild Geese in Captivity by Bob Elgas Big Timber, Montana
Wild Geese in Captivity by Bob Elgas Big Timber, Montana Man has always been fascinated by, Wild geese were frequently depicted exists, and wild geese have become and has had a close association with, on ancient structures. Indeed, the increasingly popular with avicul wild geese. As a result of their ten- Swan goose of China, and the Greylag turists. dency to vocalize an objection to of Europe were domesticated eons Throughout the world there are nocturnal disturbances, the early ago, long before the dawn of written some 15 species of wild geese, with Romans utilized them as watchdogs.. history. Even today the fascination numerous sub-species, all of which are native to the northern hemi sphere. Interestingly, there are no true geese in the southern hemisphere. South America is represented by a specialized group known as sheld geese, while Africa and Australia are represented by a number of birds with goose-like characteristics. Sheld geese are actually modified ducks which, through the evolutionary process, have assumed goose-like similarities. One of the more obvious differences is the dimorphism of sexes characterized by sheldgeese males being of completely different plumage than females. In true geese, both sexes are alike. Although the birds from the southern hemisphere are interesting in their own right, the differences are so great that they can not be classified with the true geese. The geese of the northern hemi sphere are divided into two groups the genus Anset; which is representa tive of the true geese, and the genus A representative ofthe genus Anser is thispair ofEmperorgeese (Anser canagicus). -
The All-Bird Bulletin
Advancing Integrated Bird Conservation in North America Spring 2014 Inside this issue: The All-Bird Bulletin Protecting Habitat for 4 the Buff-breasted Sandpiper in Bolivia The Neotropical Migratory Bird Conservation Conserving the “Jewels 6 Act (NMBCA): Thirteen Years of Hemispheric in the Crown” for Neotropical Migrants Bird Conservation Guy Foulks, Program Coordinator, Division of Bird Habitat Conservation, U.S. Fish and Bird Conservation in 8 Wildlife Service (USFWS) Costa Rica’s Agricultural Matrix In 2000, responding to alarming declines in many Neotropical migratory bird popu- Uruguayan Rice Fields 10 lations due to habitat loss and degradation, Congress passed the Neotropical Migra- as Wintering Habitat for tory Bird Conservation Act (NMBCA). The legislation created a unique funding Neotropical Shorebirds source to foster the cooperative conservation needed to sustain these species through all stages of their life cycles, which occur throughout the Western Hemi- Conserving Antigua’s 12 sphere. Since its first year of appropriations in 2002, the NMBCA has become in- Most Critical Bird strumental to migratory bird conservation Habitat in the Americas. Neotropical Migratory 14 Bird Conservation in the The mission of the North American Bird Heart of South America Conservation Initiative is to ensure that populations and habitats of North Ameri- Aros/Yaqui River Habi- 16 ca's birds are protected, restored, and en- tat Conservation hanced through coordinated efforts at in- ternational, national, regional, and local Strategic Conservation 18 levels, guided by sound science and effec- in the Appalachians of tive management. The NMBCA’s mission Southern Quebec is to achieve just this for over 380 Neo- tropical migratory bird species by provid- ...and more! Cerulean Warbler, a Neotropical migrant, is a ing conservation support within and be- USFWS Bird of Conservation Concern and listed as yond North America—to Latin America Vulnerable on the International Union for Conser- Coordination and editorial vation of Nature (IUCN) Red List. -
Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee
Biodiversity: the UK Overseas Territories Compiled by S. Oldfield Edited by D. Procter and L.V. Fleming ISBN: 1 86107 502 2 © Copyright Joint Nature Conservation Committee 1999 Illustrations and layout by Barry Larking Cover design Tracey Weeks Printed by CLE Citation. Procter, D., & Fleming, L.V., eds. 1999. Biodiversity: the UK Overseas Territories. Peterborough, Joint Nature Conservation Committee. Disclaimer: reference to legislation and convention texts in this document are correct to the best of our knowledge but must not be taken to infer definitive legal obligation. Cover photographs Front cover: Top right: Southern rockhopper penguin Eudyptes chrysocome chrysocome (Richard White/JNCC). The world’s largest concentrations of southern rockhopper penguin are found on the Falkland Islands. Centre left: Down Rope, Pitcairn Island, South Pacific (Deborah Procter/JNCC). The introduced rat population of Pitcairn Island has successfully been eradicated in a programme funded by the UK Government. Centre right: Male Anegada rock iguana Cyclura pinguis (Glen Gerber/FFI). The Anegada rock iguana has been the subject of a successful breeding and re-introduction programme funded by FCO and FFI in collaboration with the National Parks Trust of the British Virgin Islands. Back cover: Black-browed albatross Diomedea melanophris (Richard White/JNCC). Of the global breeding population of black-browed albatross, 80 % is found on the Falkland Islands and 10% on South Georgia. Background image on front and back cover: Shoal of fish (Charles Sheppard/Warwick -
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. -
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 ................................................................................................................................................................................................................................................. -
The Best of Costa Rica March 19–31, 2019
THE BEST OF COSTA RICA MARCH 19–31, 2019 Buffy-crowned Wood-Partridge © David Ascanio LEADERS: DAVID ASCANIO & MAURICIO CHINCHILLA LIST COMPILED BY: DAVID ASCANIO VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM THE BEST OF COSTA RICA March 19–31, 2019 By David Ascanio Photo album: https://www.flickr.com/photos/davidascanio/albums/72157706650233041 It’s about 02:00 AM in San José, and we are listening to the widespread and ubiquitous Clay-colored Robin singing outside our hotel windows. Yet, it was still too early to experience the real explosion of bird song, which usually happens after dawn. Then, after 05:30 AM, the chorus started when a vocal Great Kiskadee broke the morning silence, followed by the scratchy notes of two Hoffmann´s Woodpeckers, a nesting pair of Inca Doves, the ascending and monotonous song of the Yellow-bellied Elaenia, and the cacophony of an (apparently!) engaged pair of Rufous-naped Wrens. This was indeed a warm welcome to magical Costa Rica! To complement the first morning of birding, two boreal migrants, Baltimore Orioles and a Tennessee Warbler, joined the bird feast just outside the hotel area. Broad-billed Motmot . Photo: D. Ascanio © Victor Emanuel Nature Tours 2 The Best of Costa Rica, 2019 After breakfast, we drove towards the volcanic ring of Costa Rica. Circling the slope of Poas volcano, we eventually reached the inspiring Bosque de Paz. With its hummingbird feeders and trails transecting a beautiful moss-covered forest, this lodge offered us the opportunity to see one of Costa Rica´s most difficult-to-see Grallaridae, the Scaled Antpitta. -
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. -
Parallel Evolution in the Major Haemoglobin Genes of Eight Species of Andean Waterfowl
Molecular Ecology (2009) doi: 10.1111/j.1365-294X.2009.04352.x Parallel evolution in the major haemoglobin genes of eight species of Andean waterfowl K. G. M C CRACKEN,* C. P. BARGER,* M. BULGARELLA,* K. P. JOHNSON,† S. A. SONSTHAGEN,* J. TRUCCO,‡ T. H. VALQUI,§– R. E. WILSON,* K. WINKER* and M. D. SORENSON** *Institute of Arctic Biology, Department of Biology and Wildlife, and University of Alaska Museum, University of Alaska Fairbanks, Fairbanks, AK 99775, USA, †Illinois Natural History Survey, Champaign, IL 61820, USA, ‡Patagonia Outfitters, Perez 662, San Martin de los Andes, Neuque´n 8370, Argentina, §Centro de Ornitologı´a y Biodiversidad (CORBIDI), Sta. Rita 117, Urbana Huertos de San Antonio, Surco, Lima 33, Peru´, –Museum of Natural Science, Louisiana State University, Baton Rouge, LA 70803, USA, **Department of Biology, Boston University, Boston, MA 02215, USA Abstract Theory predicts that parallel evolution should be common when the number of beneficial mutations is limited by selective constraints on protein structure. However, confirmation is scarce in natural populations. Here we studied the major haemoglobin genes of eight Andean duck lineages and compared them to 115 other waterfowl species, including the bar-headed goose (Anser indicus) and Abyssinian blue-winged goose (Cyanochen cyanopterus), two additional species living at high altitude. One to five amino acid replacements were significantly overrepresented or derived in each highland population, and parallel substitutions were more common than in simulated sequences evolved under a neutral model. Two substitutions evolved in parallel in the aA subunit of two (Ala-a8) and five (Thr-a77) taxa, and five identical bA subunit substitutions were observed in two (Ser-b4, Glu-b94, Met-b133) or three (Ser-b13, Ser-b116) taxa.