Breeding Habitat Selection of Reeves's Pheasant
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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. -
(Syrmaticus Reevesii) Lysozyme
Agric. Biol. Chem., 55 (7), 1707-1713, 1991 1707 The AminoAcid Sequence of Reeves' Pheasant (Syrmaticus reevesii) Lysozyme Tomohiro Araki,* MayumiKuramoto and Takao Torikata Laboratory of Biochemistry, Faculty of Agriculture, Kyushu Tokai University, Aso, Kumamoto 869-14, Japan Received November 13, 1990 The amino acid sequence of reeves' pheasant lysozyme was analyzed. Carboxymethylated lysozyme was digested with trypsin and resulting peptides were analyzed using the DABITC/PITCdouble coupling manual Edmanmethod. The established amino acid sequence had seven substitutions, Tyr3, Leul5, His41, His77, Ser79, ArglO2, and Asnl21, compared with hen egg-white lysozyme. Ser79 was the first found in a bird lysozyme. A substitution in the active site was found in position 102 which has been considered to participate in the substrate binding at subsites A-C. Lysozymeis one of the most characterized and concluded that the enhancement of the hydrolases, which cleave /M,4 linkage of transglycosylation was correlated with the TV-acetylglucosamine (GlcNAc) homopolymer binding of substrate at subsite A. The substrate or GlcNAc-7V-acetylmuramic acid hetero- binding at subsite A has further been polymer. This enzyme is composed of 129-130 investigated by an NMR study.6) The co- amino acids, and the tertiary structure of hen valently bound glucosamine on AsplOl at egg-white lysozyme (HEWL) has been eluci- subsite Acaused a change of the indole proton dated by X-ray refraction study.1} The of Trp62. This result strongly suggested that mechanism of catalytic reaction of this protein the amino acid at position 101 participates in has also been elucidated in detail. The enzyme the interaction between the substrate and contains six substrate binding subsites (A-F) substrate binding site of lysozyme. -
Copper Pheasant
Bird Research News Vol.3 No.11 2006.11.10. Last Revised:2013.11.28. Copper Pheasant Yamadori (Jpn) Syrmaticus soemmerringii Morphology and classification bly smaller white part in the boundary zone between the two sub- species ranges (Kawaji 2004). Confusion between the two subspe- cies poses a problem to game hunters and government officials Classification: Galliformes Phasianidae concerned every year because ijimae has been removed from game Wing length: ♂ 205-230mm ♀ 192-219mm bird list since 1979 due to the population decline. Since subspecies Tail length: ♂ 415-952mm ♀ 164-205mm classification could become a major issue in conservation and Culmen length: ♂ 23-31mm ♀ 22-26mm social scenes in the future, genetic analyses are currently underway Tarsus length: ♂ 57-69mm ♀ 53-60mm (Sakanashi et al. 2006). Weight: ♂ 943-1348g ♀ 745-1000g Habitat: All measurement values are of subspecies Syrmaticus soemmerringii scintillans after Kiyosu (1978). Copper Pheasants are a forest dweller, generally preferring a broad -leaved forest. But they also occur in conifer plantations, such as Appearance: Japanese cedar and cypress. They occasionally bathe in the sun Plumage colors of Copper Pheasants and dust in grasslands of a cutover. vary between subspecies. In general, however, male is reddish brown on the Life history upper and underparts with black, chest- nut, yellow and white lateral bars in the 123456789101112 long tail (Photo 1). In the subspecies of breeding season non-breeding season the southern Japan (S.s. soemmerringii and ijimae), the plumage is generally Breeding system: darker with dark red brown and black Copper Pheasants are assumed to be polygamous like Common horizontal bars in the tail. -
CHAPTER 5 PRODUCTS of ANIMAL ORIGIN, NOT ELSEWHERE SPECIFIED OR INCLUDED I 5-1 Notes: 1
)&f1y3X CHAPTER 5 PRODUCTS OF ANIMAL ORIGIN, NOT ELSEWHERE SPECIFIED OR INCLUDED I 5-1 Notes: 1. This chapter does not cover: (a) Edible products (other than guts, bladders and stomachs of animals, whole and pieces thereof, and animal blood, liquid or dried); (b) Hides or skins (including furskins) other than goods of heading 0505 and parings and simlar waste of raw hides or skins of heading 0511 (chapter 41 or 43); (c) Animal textile materials, other than horsehair and horsehair waste (section XI); or (d) Prepared knots or tufts for broom or brush making (heading 9603). 2. For the purposes of heading 0501, the sorting of hair by length (provided the root ends and tip ends, respectively, are not arranged together) shall be deemed not to constitute working. 3. Throughout the tariff schedule, elephant, walrus, narwhal and wild boar tusks, rhinoceros horns and the teeth of all animals are regarded as "ivory." 4. Throughout the tariff schedule, the expression "horsehair" means hair of the manes or tails of equine or bovine animals. Additional U.S. Note 1. (a) Except as provided in paragraphs (b) and (c) of this note, the importation of the feathers or skin of any bird is hereby prohibited. Such prohibition shall apply to the feathers or skin of any bird: (i) Whether raw or processed; (ii) Whether the whole plumage or skin or any part of either; (iii) Whether or not attached to a whole bird or any part thereof; and (iv) Whether or not forming part of another article. (b) Paragraph (a) shall not apply: (i) In respect of any of the following birds (other than any such bird which, whether or not raised in captivity, is a wild bird): chickens (including hens and roosters), turkeys, guineas, geese, ducks, pigeons, ostriches, rheas, English ring-necked pheasants and pea fowl; (ii) To any importation for scientific or educational purposes; (iii) To the importation of fully manufactured artificial flies used for fishing; (iv) To the importation of birds which are classifiable under subheading 9804.00.55; and (v) To the importation of live birds. -
Phylogeography of the Common Pheasant Phasianus Colchinus
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/311941340 Phylogeography of the Common Pheasant Phasianus colchinus Article in Ibis · February 2017 DOI: 10.1111/ibi.12455 CITATION READS 1 156 5 authors, including: Nasrin Kayvanfar Mansour Aliabadian Ferdowsi University Of Mashhad Ferdowsi University Of Mashhad 7 PUBLICATIONS 39 CITATIONS 178 PUBLICATIONS 529 CITATIONS SEE PROFILE SEE PROFILE Zheng-Wang Zhang Yang Liu Beijing Normal University Sun Yat-Sen University 143 PUBLICATIONS 827 CITATIONS 53 PUBLICATIONS 286 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Using of microvertebrate remains in reconstruction of late quaternary (Holocene) paleoclimate, Eastern Iran View project Spatial distribution and composition of aliphatic hydrocarbons, polycyclic aromatic hydrocarbons and hopanes in superficial sediments of the coral reefs of the Persian Gulf, Iran View project All content following this page was uploaded by Yang Liu on 05 March 2017. The user has requested enhancement of the downloaded file. All in-text references underlined in blue are added to the original document and are linked to publications on ResearchGate, letting you access and read them immediately. Ibis (2016), doi: 10.1111/ibi.12455 Phylogeography of the Common Pheasant Phasianus colchicus NASRIN KAYVANFAR,1 MANSOUR ALIABADIAN,1,2* XIAOJU NIU,3 ZHENGWANG ZHANG3 & YANG LIU4* 1Department of Biology, Faculty of Science, Ferdowsi University -
Phylogenetic Relationships of the Phasianidae Reveals Possible Non-Pheasant Taxa
Journal of Heredity 2003:94(6):472–489 Ó 2003 The American Genetic Association DOI: 10.1093/jhered/esg092 Phylogenetic Relationships of the Phasianidae Reveals Possible Non-Pheasant Taxa K. L. BUSH AND C. STROBECK From the Department of Biological Sciences, University of Alberta–Edmonton, Edmonton, Alberta T6G 2E9, Canada. Address correspondence to Krista Bush at the address above, or e-mail: [email protected]. Abstract The phylogenetic relationships of 21 pheasant and 6 non-pheasant species were determined using nucleotide sequences from the mitochondrial cytochrome b gene. Maximum parsimony and maximum likelihood analysis were used to try to resolve the phylogenetic relationships within Phasianidae. Both the degree of resolution and strength of support are improved over previous studies due to the testing of a number of species from multiple pheasant genera, but several major ambiguities persist. Polyplectron bicalcaratum (grey peacock pheasant) is shown not to be a pheasant. Alternatively, it appears ancestral to either the partridges or peafowl. Pucrasia macrolopha macrolopha (koklass) and Gallus gallus (red jungle fowl) both emerge as non-pheasant genera. Monophyly of the pheasant group is challenged if Pucrasia macrolopha macrolopha and Gallus gallus are considered to be pheasants. The placement of Catreus wallichii (cheer) within the pheasants also remains undetermined, as does the cause for the great sequence divergence in Chrysolophus pictus obscurus (black-throated golden). These results suggest that alterations in taxonomic -
31St August 2021 Name and Address of Collection/Breeder: Do You Closed Ring Your Young Birds? Yes / No
Page 1 of 3 WPA Census 2021 World Pheasant Association Conservation Breeding Advisory Group 31st August 2021 Name and address of collection/breeder: Do you closed ring your young birds? Yes / No Adults Juveniles Common name Latin name M F M F ? Breeding Pairs YOUNG 12 MTH+ Pheasants Satyr tragopan Tragopan satyra Satyr tragopan (TRS ringed) Tragopan satyra Temminck's tragopan Tragopan temminckii Temminck's tragopan (TRT ringed) Tragopan temminckii Cabot's tragopan Tragopan caboti Cabot's tragopan (TRT ringed) Tragopan caboti Koklass pheasant Pucrasia macrolopha Himalayan monal Lophophorus impeyanus Red junglefowl Gallus gallus Ceylon junglefowl Gallus lafayettei Grey junglefowl Gallus sonneratii Green junglefowl Gallus varius White-crested kalij pheasant Lophura l. hamiltoni Nepal Kalij pheasant Lophura l. leucomelana Crawfurd's kalij pheasant Lophura l. crawfurdi Lineated kalij pheasant Lophura l. lineata True silver pheasant Lophura n. nycthemera Berlioz’s silver pheasant Lophura n. berliozi Lewis’s silver pheasant Lophura n. lewisi Edwards's pheasant Lophura edwardsi edwardsi Vietnamese pheasant Lophura e. hatinhensis Swinhoe's pheasant Lophura swinhoii Salvadori's pheasant Lophura inornata Malaysian crestless fireback Lophura e. erythrophthalma Bornean crested fireback pheasant Lophura i. ignita/nobilis Malaysian crestless fireback/Vieillot's Pheasant Lophura i. rufa Siamese fireback pheasant Lophura diardi Southern Cavcasus Phasianus C. colchicus Manchurian Ring Neck Phasianus C. pallasi Northern Japanese Green Phasianus versicolor -
Recognizing Decorative Body Feathers of Pheasants and Related Birds
Citation: Trail, P.W. 2006. Recognizing Decorative Body Feathers of Pheasants and Related Birds. Identification Guides for Wildlife Law Enforcement No. 9. USFWS, National Fish and Wildlife Forensics Laboratory, Ashland, OR. Recognizing Decorative Body Feathers of Pheasants and Related Birds Identification Guides for Wildlife Law Enforcement No. 9 Pepper W. Trail U.S. Fish and Wildlife Service National Fish and Wildlife Forensics Laboratory 1490 East Main Street Ashland, OR 97520 [email protected] July 2006 The colorful body feathers of chickens, pheasants, guineafowl, and related birds are often used to decorate earrings, hair ties, dreamcatchers, and other small crafted items. None of these species are native to North America, and none are listed under the Endangered Species Act or CITES. Familiarity with these feathers will allow Special Agents and Wildlife Inspectors to recognize the legal use of decorative feathers and to avoid unnecessary seizures. The birds frequently used for such decorative items include the following: • Chicken (Gallus gallus) • Indian Peafowl (Pavo cristatus) • Ring-necked Pheasant (Phasianus colchicus) • Golden Pheasant (Chrysolophus pictus) • Lady Amherst Pheasant (Chrysolophus amherstiae) • Reeve’s Pheasant (Syrmaticus reevesii) • Silver Pheasant (Lophura nycthemera) • Helmeted Guineafowl (Numida meleagris) • Vulturine Guineafowl (Acryllium vulturinum) In the following pages, an assortment of body feathers from each of these species is illustrated. Many male pheasants exhibit a variety of different colors and patterns on their body feathers, and an attempt has been made to illustrate the range of types for each species. In addition, the many domestic breeds of chickens vary greatly in plumage, and so chicken feathers are very diverse in appearance, as shown. -
New Sites for Mrs Hume's Pheasant Syrmaticus Humiae in North-East
Forktail 21 (2005) SHORT NOTES 183 New sites for Mrs Hume’s Pheasant Syrmaticus humiae in north-east India based on hunters’ specimens and local reports ANWARUDDIN CHOUDHURY Mrs Hume’s Pheasant Syrmaticus humiae is a poorly DISTRIBUTION known globally threatened (Vulnerable) species (BirdLife International 2004). It is thinly distributed in I observed the species at three previously known sites the hill tracts of north-eastern India, north and west (Shiroi, Murlen and Phawngpui), recorded 20 new Myanmar, south-west China and north Thailand (Ali sites based on live captured birds or preserved speci- and Ripley 1987, Fuller and Garson 2000, Han Lian- mens in villages, and identified an additional 24 new xian 1997).Very little current information on its status sites where villagers reported the species (Appendix, and distribution is available (Fuller and Garson 2000, Fig. 1). In Nagaland, BirdLife International (2001) BirdLife International 2001). Recent fieldwork in north-east India prior to this study had resulted in few records (Katju 1996, Kaul et al. 1996, Choudhury 1997, 1998, 2000, 2001, Robson 1999). No previous survey had specifically targeted the species. I carried out surveys in Nagaland, Manipur and Mizoram during 1996–2004 to assess the current distribution and status of the species, mainly from hunters’ specimens and local reports. METHODS I carried out surveys in: Nagaland in June 1996, January, February, April and October 2001, February 2002 and February 2004; Manipur in January 1996, January 2001, October 2001 and February 2002; and Mizoram in April 2000 and February 2001. These states are almost entirely mountainous. The climate is monsoonal with hot wet summers and cool dry winters (although winter rains are also not uncommon); annual rainfall is 1,000–6,000 mm. -
A Multigene Phylogeny of Galliformes Supports a Single Origin of Erectile Ability in Non-Feathered Facial Traits
J. Avian Biol. 39: 438Á445, 2008 doi: 10.1111/j.2008.0908-8857.04270.x # 2008 The Authors. J. Compilation # 2008 J. Avian Biol. Received 14 May 2007, accepted 5 November 2007 A multigene phylogeny of Galliformes supports a single origin of erectile ability in non-feathered facial traits Rebecca T. Kimball and Edward L. Braun R. T. Kimball (correspondence) and E. L. Braun, Dept. of Zoology, Univ. of Florida, P.O. Box 118525, Gainesville, FL 32611 USA. E-mail: [email protected] Many species in the avian order Galliformes have bare (or ‘‘fleshy’’) regions on their head, ranging from simple featherless regions to specialized structures such as combs or wattles. Sexual selection for these traits has been demonstrated in several species within the largest galliform family, the Phasianidae, though it has also been suggested that such traits are important in heat loss. These fleshy traits exhibit substantial variation in shape, color, location and use in displays, raising the question of whether these traits are homologous. To examine the evolution of fleshy traits, we estimated the phylogeny of galliforms using sequences from four nuclear loci and two mitochondrial regions. The resulting phylogeny suggests multiple gains and/or losses of fleshy traits. However, it also indicated that the ability to erect rapidly the fleshy traits is restricted to a single, well-supported lineage that includes species such as the wild turkey Meleagris gallopavo and ring-necked pheasant Phasianus colchicus. The most parsimonious interpretation of this result is a single evolution of the physiological mechanisms that underlie trait erection despite the variation in color, location, and structure of fleshy traits that suggest other aspects of the traits may not be homologous. -
Intergeneric Galliform Hybrids: a Review
INTERGENERIC GALLIFORM HYBRIDS : A REVIEW BY TONY J. PETERLE Henry Seebohm, in “The Birds of Siberia” (1901: Sol-502), makes this cogent observa- tion: “The subject of the interbreeding of nearly-allied birds in certain localities where their geographical ranges meet or overlap, and the almost identical subject of the existence of intermediate forms in the intervening district between the respective geographical ranges of nearly-allied birds, is one which has not yet received the attention which it deserves from ornithologists. The older brethren of the fraternity have always pooh-pooh’d any attempt to explain some of these complicated facts of nature by the theory of interbreeding, and have looked upon the suggestion that hybridisation was anything but an abnormal circumstance as one of the lamest modes of getting out of an ornithological difficulty.” The following sum- mary will show that interbreeding of galliform genera has often been observed: indeed that two wholly different intergeneric hybrids, one of the Old World, one of the New, have been recovered so often that they can hardly be considered ‘abnormal’ except in a very limited sense. The Old World hybrid referred to results from the crossing of the Blackcock (Lyvurus) and Capercaillie (Tetrao). DeWinton (1894: 448) said that “of all hybrids among birds in a wild state this one seems to be the most frequent.” Authors seem to be in agreement that the hybrid results principally, if not always, from the interbreeding of male Lyrurus with fe- male Tetreo in areas throughout which (a) extension of range is taking place, or (b) one or the other genus is rare, e.g., Scotland, where Tetrao has been introduced following extirpation (Millais, 1906: 55-56; DeWinton, 1894). -
The Introduced Silver Pheasant (Lophura Nycthemera) in Patagonia: Abundance, Group Structure, Activity Patterns and Association to Human Disturbance
2017Hornero 32(2):227–236, 2017 SILVER PHEASANT IN PATAGONIA 227 THE INTRODUCED SILVER PHEASANT (LOPHURA NYCTHEMERA) IN PATAGONIA: ABUNDANCE, GROUP STRUCTURE, ACTIVITY PATTERNS AND ASSOCIATION TO HUMAN DISTURBANCE VALERIA L. MARTIN-ALBARRACIN 1,3, GUILLERMO C. AMICO 1 AND MARTÍN A. NUÑEZ 2 1 Laboratorio Ecotono, INIBIOMA, CONICET-Universidad Nacional del Comahue. Quintral 1250, 8400 San Carlos de Bariloche, Río Negro, Argentina. 2 Grupo de Ecología de Invasiones, INIBIOMA, CONICET-Universidad Nacional del Comahue. Av. de los Pioneros 2350, San Carlos de Bariloche, Río Negro, Argentina. 3 [email protected] ABSTRACT.— Phasianids are one of the groups of introduced birds with highest impact on native ecosystems. In Patagonia several phasianids are established or in process of establishment, thus it is relevant to know their impacts on ecosystems. The Silver Pheasant (Lophura nycthemera) was introduced to Isla Victoria in the 1950’s and successfully established all over the island. The aim of this work is to study the population of this species on Isla Victoria in terms of abundance and association to human disturbance as a first step to know its potential impact in the ecosystem. We conducted camera-trapping and direct observations in linear transects located in highly dis- turbed and in lowly disturbed areas. Using camera-trapping data we estimated an index of rela- tive abundance to compare habitat use between areas. We used the distance-sampling approach to estimate population density with the data from direct observations. The Silver Pheasant used much more frequently areas with a high level of disturbance, suggesting that the presence of disturbed habitats could facilitate establishment and spread of this species in Patagonia.