Captive Breeding Symposium
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Nogth AMERICAN BIRDS
CHECK-LIST OF NOgTH AMERICAN BIRDS The Speciesof Birds of North America from the Arctic through Panama, Including the West Indies and Hawaiian Islands PREPARED BY THE COMMITTEE ON CLASSIFICATION AND NOMENCLATURE OF THE AMERICAN ORNITHOLOGISTS' UNION SEVENTH EDITION 1998 Zo61ogical nomenclature is a means, not an end, to Zo61ogical Science PUBLISHED BY THE AMERICAN ORNITHOLOGISTS' UNION 1998 Copyright 1998 by The American Ornithologists' Union All rights reserved, except that pages or sections may be quoted for research purposes. ISBN Number: 1-891276-00-X Preferred citation: American Ornithologists' Union. 1983. Check-list of North American Birds. 7th edition. American Ornithologists' Union, Washington, D.C. Printed by Allen Press, Inc. Lawrence, Kansas, U.S.A. CONTENTS DEDICATION ...................................................... viii PREFACE ......................................................... ix LIST OF SPECIES ................................................... xvii THE CHECK-LIST ................................................... 1 I. Tinamiformes ............................................. 1 1. Tinamidae: Tinamous .................................. 1 II. Gaviiformes .............................................. 3 1. Gaviidae: Loons ....................................... 3 III. Podicipediformes.......................................... 5 1. Podicipedidae:Grebes .................................. 5 IV. Procellariiformes .......................................... 9 1. Diomedeidae: Albatrosses ............................. -
CITES Cop16 Prop. 17 IUCN-TRAFFIC Analysis (PDF, 88KB)
Ref. CoP16 Prop. 17 Deletion of Imperial Pheasant Lophura imperialis from Appendix I Proponent: Switzerland, as Depositary Government, at the request of the Animals Committee (prepared by France) Summary: The Imperial Pheasant Lophura imperialis is a rare dark-blue pheasant known in the wild from just four records from Viet Nam. First described in 1924 from a single live pair, it is now accepted as being an occasional naturally-occurring hybrid between Silver Pheasant L. nycthemera and Edward’s Pheasant L. edwardsi. A bird captured in 1990 was likely a hybrid between L. nycthemera and Vietnamese Pheasant L. hatinhensis which itself has been found to be an inbred form of L. edwardsi. There have been no other confirmed reports of Imperial Pheasant in the wild. A captive stock was established in Europe and the USA from a pair caught in 1923, which were subsequently cross-bred with Lophura nycthemera to create new stock. Birds with Imperial Pheasant phenotype have also been created in captivity by hybridizing Silver Pheasant and Edward’s Pheasant. Lophura imperialis and L. edwardsi were both listed in CITES Appendix I in 1975. Since 1975 international trade in 31 L. imperialis individuals has been reported in the CITES trade database, all but four declared as captive-bred. These four comprise animals exported before 1999 from non-range States with no source code included in the record. There is no reason to suppose that these were not also captive-bred. Lophura imperialis is proposed for removal from Appendix I on the basis that it is no longer recognised as a species. -
Status of Galliformes in Pipar Pheasant Reserve and Santel, Annapurna, Nepal
Status of Galliformes in Pipar Pheasant Reserve and Santel, Annapurna, Nepal 1 2 3 4 LAXMAN P. POUDYAL *, NAVEEN K. MAHATO , PARAS B. SINGH , POORNESWAR SUBEDI , HEM S. BARAL 5 and PHILIP J. K. MCGOWAN 6 1 Department of National Parks and Wildlife Conservation, PO Box 860, Babarmahal, Kathmandu, Nepal. 2 Red Panda Network – Nepal, PO Box 21477, Kathmandu, Nepal. 3 Biodiversity Conservation Society, PO Box 24304, Kathmandu, Nepal. 4 Department of Forests, Kathmandu, Nepal. 5 Bird Conservation Nepal, PO Box 12465, Lazimpat, Kathmandu, Nepal. 6 World Pheasant Association, Newcastle University Biology Field Station, Close House Estate, Heddon on the Wall, Newcastle upon Tyne, NE15 0HT UK. *Correspondence author - [email protected] Paper presented at the 4 th International Galliformes Symposium, 2007, Chengdu, China. Abstract The Galliformes of Pipar have been surveyed seven times between 1979 and 1998. The nearby area of Santel was surveyed using comparable methods in 2001. In continuance of the long- term monitoring at Pipar and to provide a second count at Santel, dawn call counts were conducted in both areas, using the same survey points as previous surveys, between 29 th April and 9 th May 2005. The aim of those surveys was to collect information on the status of pheasants and partridges and to look for any changes over time. In both areas, galliform numbers were higher in 2005 than in previous surveys, for most species. For each species there was no evidence of decline since the first counts were conducted nearly 30 years ago. Both areas provide good habitat for Galliformes and disturbance is not a serious issue. -
Melagiris (Tamil Nadu)
MELAGIRIS (TAMIL NADU) PROPOSAL FOR IMPORTANT BIRD AREA (IBA) State : Tamil Nadu, India District : Krishnagiri, Dharmapuri Coordinates : 12°18©54"N 77°41©42"E Ownership : State Area : 98926.175 ha Altitude : 300-1395 m Rainfall : 620-1000 mm Temperature : 10°C - 35°C Biographic Zone : Deccan Peninsula Habitats : Tropical Dry Deciduous, Riverine Vegetation, Tropical Dry Evergreen Proposed Criteria A1 (Globally Threatened Species) A2 (Endemic Bird Area 123 - Western Ghats, Secondary Area s072 - Southern Deccan Plateau) A3 (Biome-10 - Indian Peninsula Tropical Moist Forest, Biome-11 - Indo-Malayan Tropical Dry Zone) GENERAL DESCRIPTION The Melagiris are a group of hills lying nestled between the Cauvery and Chinnar rivers, to the south-east of Hosur taluk in Tamil Nadu, India. The Melagiris form part of an almost unbroken stretch of forests connecting Bannerghatta National Park (which forms its north-western boundary) to the forests of Cauvery Wildlife Sanctuary - Karnataka (which forms its southern boundary, separated by the river Cauvery), and further to Biligirirangan hills and Sathyamangalam forests. The northern and western parts are comparatively plain and is part of the Mysore plateau. The average elevation in this region is 500-1000 m. Ground sinks to 300m in the valley of the Cauvery and the highest point is the peak of Guthereyan at 1395.11 m. Red sandy loam is the most common soil type found in this region. Small deposits of alluvium are found along Cauvery and Chinnar rivers and Kaoline is found in some areas near Jowlagiri. The temperature ranges from 10°C ± 35°C. South-west monsoon is fairly active mostly in the northern areas, but north-east monsoon is distinctly more effective in the region. -
2011, Article ID 423938, 16 Pages Doi:10.4061/2011/423938
SAGE-Hindawi Access to Research International Journal of Evolutionary Biology Volume 2011, Article ID 423938, 16 pages doi:10.4061/2011/423938 Research Article A Macroevolutionary Perspective on Multiple Sexual Traits in the Phasianidae (Galliformes) Rebecca T. Kimball, Colette M. St. Mary, and Edward L. Braun Department of Biology, University of Florida, P.O. Box 118525, Gainesville, FL 32611, USA Correspondence should be addressed to Rebecca T. Kimball, [email protected]fl.edu Received 2 October 2010; Accepted 26 February 2011 Academic Editor: Rob Kulathinal Copyright © 2011 Rebecca T. Kimball et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Traits involved in sexual signaling are ubiquitous among animals. Although a single trait appears sufficient to convey information, many sexually dimorphic species exhibit multiple sexual signals, which may be costly to signalers and receivers. Given that one signal may be enough, there are many microevolutionary hypotheses to explain the evolution of multiple signals. Here we extend these hypotheses to a macroevolutionary scale and compare those predictions to the patterns of gains and losses of sexual dimorphism in pheasants and partridges. Among nine dimorphic characters, including six intersexual signals and three indicators of competitive ability, all exhibited both gains and losses of dimorphism within the group. Although theories of intersexual selection emphasize gain and elaboration, those six characters exhibited greater rates of loss than gain; in contrast, the competitive traits showed a slight bias towards gains. The available models, when examined in a macroevolutionary framework, did not yield unique predictions, making it difficult to distinguish among them. -
A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes)
Galliform Baraminology 1 Running Head: GALLIFORM BARAMINOLOGY A Baraminological Analysis of the Land Fowl (Class Aves, Order Galliformes) Michelle McConnachie A Senior Thesis submitted in partial fulfillment of the requirements for graduation in the Honors Program Liberty University Spring 2007 Galliform Baraminology 2 Acceptance of Senior Honors Thesis This Senior Honors Thesis is accepted in partial fulfillment of the requirements for graduation from the Honors Program of Liberty University. ______________________________ Timothy R. Brophy, Ph.D. Chairman of Thesis ______________________________ Marcus R. Ross, Ph.D. Committee Member ______________________________ Harvey D. Hartman, Th.D. Committee Member ______________________________ Judy R. Sandlin, Ph.D. Assistant Honors Program Director ______________________________ Date Galliform Baraminology 3 Acknowledgements I would like to thank my Lord and Savior, Jesus Christ, without Whom I would not have had the opportunity of being at this institution or producing this thesis. I would also like to thank my entire committee including Dr. Timothy Brophy, Dr. Marcus Ross, Dr. Harvey Hartman, and Dr. Judy Sandlin. I would especially like to thank Dr. Brophy who patiently guided me through the entire research and writing process and put in many hours working with me on this thesis. Finally, I would like to thank my family for their interest in this project and Robby Mullis for his constant encouragement. Galliform Baraminology 4 Abstract This study investigates the number of galliform bird holobaramins. Criteria used to determine the members of any given holobaramin included a biblical word analysis, statistical baraminology, and hybridization. The biblical search yielded limited biosystematic information; however, since it is a necessary and useful part of baraminology research it is both included and discussed. -
Partridges, Quails, Pheasants and Turkeys Phasianidae Vigors, 1825: Zoological Journal 2: 402 – Type Genus Phasianus Linnaeus, 1758
D .W . .5 / DY a 5D t w[ { wt Ç"" " !W5 í ÇI &'(' / b ù b a L w 5 ! ) " í "* " Ç t+ t " h " * { b ù" t* &)/&0 Order GALLIFORMES: Game Birds and Allies The order of galliform taxa in Checklist Committee (1990) appears to have been based on Peters (1934). Johnsgard (1986) synthesised available data, came up with similar groupings of taxa, and produced a dendrogram indicating that turkeys (Meleagridinae) were the most primitive (outside Cracidae and Megapodiidae), with grouse (Tetraoninae), guineafowl (Numidinae), New World quails (Odontophorinae) and pheasants and kin (Phasianinae) successively more derived. Genetic evidence (DNA-hybridisation data) provided by Sibley & Ahlquist (1990) suggested Odontophorinae were the most basal phasianoids and guineafowl the next most basal group. A basal position of the New World quails among phasianoids has been supported by other genetic data (Kimball et al. 1999, Armstrong et al. 2001). A recent analysis based on morphological characters (Dyke et al. 2003) found support for megapodes as the most basal group in the order, then Cracidae, then Phasianidoidea, and within the latter, Numididae the most basal group. In contrast to the above genetic-based analyses, Dyke et al. (2003) found the Odontophorinae to be the most derived group within the order. A recent analysis using both mitochondrial ND2 and cytochrome-b DNA sequences, however, reinforces the basal position of the Odontophorinae (Pereira & Baker 2006). Here we follow a consensus of the above works and place Odontophorinae basal in the phasianids. Worthy & Holdaway (2002) considered that Cheeseman’s (1891) second-hand record of megapodes from Raoul Island, Kermadec Group, before the 1870 volcanic eruption has veracity. -
Hybridization & Zoogeographic Patterns in Pheasants
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Paul Johnsgard Collection Papers in the Biological Sciences 1983 Hybridization & Zoogeographic Patterns in Pheasants Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/johnsgard Part of the Ornithology Commons Johnsgard, Paul A., "Hybridization & Zoogeographic Patterns in Pheasants" (1983). Paul Johnsgard Collection. 17. https://digitalcommons.unl.edu/johnsgard/17 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 Paul Johnsgard Collection by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. HYBRIDIZATION & ZOOGEOGRAPHIC PATTERNS IN PHEASANTS PAUL A. JOHNSGARD The purpose of this paper is to infonn members of the W.P.A. of an unusual scientific use of the extent and significance of hybridization among pheasants (tribe Phasianini in the proposed classification of Johnsgard~ 1973). This has occasionally occurred naturally, as for example between such locally sympatric species pairs as the kalij (Lophura leucol11elana) and the silver pheasant (L. nycthelnera), but usually occurs "'accidentally" in captive birds, especially in the absence of conspecific mates. Rarely has it been specifically planned for scientific purposes, such as for obtaining genetic, morphological, or biochemical information on hybrid haemoglobins (Brush. 1967), trans ferins (Crozier, 1967), or immunoelectrophoretic comparisons of blood sera (Sato, Ishi and HiraI, 1967). The literature has been summarized by Gray (1958), Delacour (1977), and Rutgers and Norris (1970). Some of these alleged hybrids, especially those not involving other Galliformes, were inadequately doculnented, and in a few cases such as a supposed hybrid between domestic fowl (Gallus gal/us) and the lyrebird (Menura novaehollandiae) can be discounted. -
Phylogeography of the Bobwhites
PHYLOGEOGRAPHY OF THE BOBWHITES Damon Williford, Randy W. DeYoung, Leonard A. Brennan, Fidel Hernández Caesar Kleberg Wildlife Research Institute Texas A&M University-Kingsville Kingsville, Texas 78363 Rodney L. Honeycutt Natural Science Division Pepperdine University California 90263 The Bobwhites (Colinus): Savanna-specialists Yucatán Bobwhite (Colinus nigrogularis) Northern Bobwhite (Colinus virginianus) Photo by David Blank Photo by Ryan Shaw Spot-bellied Bobwhite (Colinus leucopogon) Crested Bobwhite (Colinus cristatus) Photo by Elidier Vargas Photo by Karla Perez Leon Spot-bellied Bobwhite Spot-bellied 6 subspecies Subspecies Distributions Bobwhite Crested Bobwhite 14 subspecies Northern Bobwhite 19 Subspecies Yucatán Bobwhite 4 subspecies Geographic Variation in Bobwhites Unanswered Questions • How many bobwhite species are there? • How are those species related to one another? • How distinct are the subspecies within each bobwhite species? • Biogeographic and evolutionary history? Phylogenetics and Phylogeography • Phylogenetics: evolutionary relationships among groups. • Phylogeography • Geographic distribution of genetic genealogies. • Infer causes of observed patterns. • Mitochondrial DNA (mtDNA) • Great initial genetic marker. • Maternal inheritance • No recombination Phylogeographic Patterns Objectives • Examine the interspecific relationships among the bobwhite species using mtDNA. • Examine phylogeography of each species. • Determine how much genetic variation is accounted for by subspecies taxonomy. • Use findings to infer -
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 Version Available for Download From
Information Sheet on Ramsar Wetlands (RIS) – 2009-2012 version Available for download from http://www.ramsar.org/ris/key_ris_index.htm. Categories approved by Recommendation 4.7 (1990), as amended by Resolution VIII.13 of the 8th Conference of the Contracting Parties (2002) and Resolutions IX.1 Annex B, IX.6, IX.21 and IX. 22 of the 9th Conference of the Contracting Parties (2005). Notes for compilers: 1. The RIS should be completed in accordance with the attached Explanatory Notes and Guidelines for completing the Information Sheet on Ramsar Wetlands. Compilers are strongly advised to read this guidance before filling in the RIS. 2. Further information and guidance in support of Ramsar site designations are provided in the Strategic Framework and guidelines for the future development of the List of Wetlands of International Importance (Ramsar Wise Use Handbook 14, 3rd edition). A 4th edition of the Handbook is in preparation and will be available in 2009. 3. Once completed, the RIS (and accompanying map(s)) should be submitted to the Ramsar Secretariat. Compilers should provide an electronic (MS Word) copy of the RIS and, where possible, digital copies of all maps. 1. Name and address of the compiler of this form: FOR OFFICE USE ONLY. DD MM YY Beatriz de Aquino Ribeiro - Bióloga - Analista Ambiental / [email protected], (95) Designation date Site Reference Number 99136-0940. Antonio Lisboa - Geógrafo - MSc. Biogeografia - Analista Ambiental / [email protected], (95) 99137-1192. Instituto Chico Mendes de Conservação da Biodiversidade - ICMBio Rua Alfredo Cruz, 283, Centro, Boa Vista -RR. CEP: 69.301-140 2. -
TRAFFIC POST Galliformes in Illegal Wildlife Trade in India: a Bird's Eye View in FOCUS TRAFFIC Post
T R A F F I C NEWSLETTER ON WILDLIFE TRADE IN INDIA N E W S L E T T E R Issue 29 SPECIAL ISSUE ON BIRDS MAY 2018 TRAFFIC POST Galliformes in illegal wildlife trade in India: A bird's eye view IN FOCUS TRAFFIC Post TRAFFIC’s newsletter on wildlife trade in India was started in September 2007 with a primary objective to create awareness about poaching and illegal wildlife trade . Illegal wildlife trade is reportedly the fourth largest global illegal trade after narcotics, counterfeiting and human trafficking. It has evolved into an organized activity threatening the future of many wildlife species. TRAFFIC Post was born out of the need to reach out to various stakeholders including decision makers, enforcement officials, judiciary and consumers about the extent of illegal wildlife trade in India and the damaging effect it could be having on the endangered flora and fauna. Since its inception, TRAFFIC Post has highlighted pressing issues related to illegal wildlife trade in India and globally, flagged early trends, and illuminated wildlife policies and laws. It has also focused on the status of legal trade in various medicinal plant and timber species that need sustainable management for ensuring ecological and economic success. TRAFFIC Post comes out three times in the year and is available both online and in print. You can subscribe to it by writing to [email protected] All issues of TRAFFIC Post can be viewed at www.trafficindia.org; www.traffic.org Map Disclaimer: The designations of the geographical entities in this publication and the presentation of the material do not imply the expression of any opinion whatsoever on the part of WWF-India or TRAFFIC concerning the legal status of any country, territory, or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. -
Alectoris Chukar
PEST RISK ASSESSMENT Chukar partridge Alectoris chukar (Photo: courtesy of Olaf Oliviero Riemer. Image from Wikimedia Commons under a Creative Commons Attribution License, Version 3.) March 2011 This publication should be cited as: Latitude 42 (2011) Pest Risk Assessment: Chukar partridge (Alectoris chukar). Latitude 42 Environmental Consultants Pty Ltd. Hobart, Tasmania. About this Pest Risk Assessment This pest risk assessment is developed in accordance with the Policy and Procedures for the Import, Movement and Keeping of Vertebrate Wildlife in Tasmania (DPIPWE 2011). The policy and procedures set out conditions and restrictions for the importation of controlled animals pursuant to s32 of the Nature Conservation Act 2002. For more information about this Pest Risk Assessment, please contact: Wildlife Management Branch Department of Primary Industries, Parks, Water and Environment Address: GPO Box 44, Hobart, TAS. 7001, Australia. Phone: 1300 386 550 Email: [email protected] Visit: www.dpipwe.tas.gov.au Disclaimer The information provided in this Pest Risk Assessment is provided in good faith. The Crown, its officers, employees and agents do not accept liability however arising, including liability for negligence, for any loss resulting from the use of or reliance upon the information in this Pest Risk Assessment and/or reliance on its availability at any time. Pest Risk Assessment: Chukar partridge Alectoris chukar 2/20 1. Summary The chukar partridge (Alectoris chukar) is native to the mountainous regions of Asia, Western Europe and the Middle East (Robinson 2007, Wikipedia 2009). Its natural range includes Turkey, the Mediterranean islands, Iran and east through Russia and China and south into Pakistan and Nepal (Cowell 2008).