CHAPTER 5 PRODUCTS of ANIMAL ORIGIN, NOT ELSEWHERE SPECIFIED OR INCLUDED I 5-1 Notes: 1
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Scottish Birds 22: 9-19
Scottish Birds THE JOURNAL OF THE SOC Vol 22 No 1 June 2001 Roof and ground nesting Eurasian Oystercatchers in Aberdeen The contrasting status of Ring Ouzels in 2 areas of upper Deeside The distribution of Crested Tits in Scotland during the 1990s Western Capercaillie captures in snares Amendments to the Scottish List Scottish List: species and subspecies Breeding biology of Ring Ouzels in Glen Esk Scottish Birds The Journal of the Scottish Ornithologists' Club Editor: Dr S da Prato Assisted by: Dr I Bainbridge, Professor D Jenkins, Dr M Marquiss, Dr J B Nelson, and R Swann Business Editor: The Secretary sac, 21 Regent Terrace Edinburgh EH7 5BT (tel 0131-5566042, fax 0131 5589947, email [email protected]). Scottish Birds, the official journal of the Scottish Ornithologists' Club, publishes original material relating to ornithology in Scotland. Papers and notes should be sent to The Editor, Scottish Birds, 21 Regent Terrace, Edinburgh EH7 SBT. Two issues of Scottish Birds are published each year, in June and in December. Scottish Birds is issued free to members of the Scottish Ornithologists' Club, who also receive the quarterly newsletter Scottish Bird News, the annual Scottish Bird Report and the annual Raplor round up. These are available to Institutions at a subscription rate (1997) of £36. The Scottish Ornithologists' Club was formed in 1936 to encourage all aspects of ornithology in Scotland. It has local branches which meet in Aberdeen, Ayr, the Borders, Dumfries, Dundee, Edinburgh, Glasgow, Inverness, New Galloway, Orkney, St Andrews, Stirling, Stranraer and Thurso, each with its own programme of field meetings and winter lectures. -
Changes to Category C of the British List†
Ibis (2005), 147, 803–820 Blackwell Publishing, Ltd. Changes to Category C of the British List† STEVE P. DUDLEY* British Ornithologists’ Union, Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK In its maintenance of the British List, the British Ornithologists’ Union Records Committee (BOURC) is responsible for assigning species to categories to indicate their status on the List. In 1995, the British Ornithologists’ Union (BOU) and the Joint Nature Conservation Committee (JNCC) held a conference on naturalized and introduced birds in Britain (Holmes & Simons 1996). This led to a review of the process of establishment of such species and the terms that best describe their status (Holmes & Stroud 1995) as well as a major review of the categorization of species on the British List (Holmes et al. 1998). The BOURC continues to review the occurrence and establishment of birds of captive origin in Britain. This paper sum- marizes the status of naturalized and introduced birds in Britain and announces changes to the categorization of many on the British List or its associated appendices (Categories D and E): Mute Swan Cygnus olor Categories AC change to AC2 Black Swan Cygnus atratus Category E* – no change Greylag Goose Anser anser Categories ACE* change to AC2C4E* Snow Goose Anser caerulescens Categories AE* change to AC2E* Greater Canada Goose Branta canadensis Categories ACE* change to C2E* Barnacle Goose Branta leucopsis Categories AE* change to AC2E* Egyptian Goose Alopochen aegyptiacus Categories CE* change -
Golden Pheasant Chrysolophus Pictus
Young Golden Pheasant Chrysolophus pictus What is the history of my relationship to man? The Golden Pheasant is commonly found in zoos and aviaries, but often as impure specimens that have the similar Lady Amherst's Pheasant in their lineage. Habitat / Climate Where am I from? dark young conifer forests The Golden Pheasant or "Chinese Pheasant",is a parrot like Map with sparse undergrowth gamebird of the order Galliformes. It is native to forests in mountainous areas of western China but feral populations have been established in the United Kingdom and elsewhere. Other family members: Caspian snowcock Who are my relatives? Gray partridge Silver Pheasant, Little chachalaca, Yellow- knobbed curassow and Western capercaillie the Turkey Breeding Potential How am I born? We lay 8-12 eggs at a time and will then incubate these for around 22-23 days. Clutch size 8 to 12 eggs When we hatch we are able to walk and look for food with in hours. By a few weeks we will loose our down and have our feathers in. How long does it take me to grow up and how long do I live Once we have gotten our feathers we will keep getting bigger. By 3 months we will be full Breeding Season grown, we might add a few pounds after that but wont get larger. We can live up to 6 years. J F M A M J J A S O N D A E A P A U U U E C O E N B R R Y N L G P T V C What kind of family life do I have? We are extremely territorial. -
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. -
Assessment of Hematological Indices of Indian Peafowl (Pavo Cristatus) Kept at Wildlife Breeding Centre, Gatwala, Faisalabad, Pakistan
Journal of Zoological Research Volume 4, Issue 1, 2020, PP 29-33 ISSN 2637-5575 Assessment of Hematological Indices of Indian Peafowl (Pavo Cristatus) Kept at Wildlife Breeding Centre, Gatwala, Faisalabad, Pakistan Misbah Sarwar1* Zahid Ali1, and Muhammad Bilal Chaudhary2 1Punjab Wildlife Research Centre, Gatwala, Faisalabad Department of Wildlife & Parks, Punjab Pakistan 2Department of Zoology, GC University, Faisalabad, Pakistan *Corresponding Author: Misbah Sarwar, Punjab Wildlife Research Centre, Gatwala, Faisalabad Department of Wildlife & Parks, Punjab Pakistan. Email: [email protected] ABSTRACT Indian peafowl (Pavo cristatus) or blue peafowl has been maintained in captivity since long where due to selective breeding, several color mutations/varieties have appeared of which white peafowl, black-shouldered peafowl and pied peafowl are common. Since, hematological analysis is crucial for clinical diagnosis of wild and captive avifauna, so we collected blood samples from healthy male blue peafowl, white peafowl and black- shouldered peafowl kept at Wildlife Breeding Centre, Gatwala, Faisalabad and compared erythrocyte and leucocyte indices among them. Our results indicated that blood physiological values for MO (%), Hgb, HCT, MCH and MCHC were significantly different (P<0.05) between blue peafowl and white peafowl whereas MCV and RDW were significantly different (P<0.05) between blue peafowl and black-shouldered peafowl. The comparison of hematological parameters between white peafowl and black-shouldered peafowl showed that GR(%), RBC, HCT, MCV and MCHC differ significantly (P<0.05) between the two varieties. Our results support the studies indicating high quality color patterns reflect increased resistance and immunity to pathogens. Keywords: Indian peafowl, Color Mutations, hematology. INTRODUCTION 2005; Takahashi and Hasegawa, 2008; Harikrishnan et al., 2010, Naseer et al., 2017). -
Why Do Eared-Pheasants of the Eastern Qinghai-Tibet Plateau Show So Much Morphological Variation?
Bird Conservation International (2000) 10:305–309. BirdLife International 2000 Why do eared-pheasants of the eastern Qinghai-Tibet plateau show so much morphological variation? XIN LU and GUANG-MEI ZHENG Summary It is known that White Eared-pheasants Crossoptilon crossoptilon drouyni interbreed widely with Tibetan Eared-pheasants C. harmani at the boundary of their ranges. A new hybrid zone has been found recently in eastern Tibet, far away from the boundary of the parental species’ ranges. Based on ecological observations of eared-pheasants and the geographical history and pattern of modern glaciers, we have attributed the complex morphological variation of eared-pheasants and the high biodiversity of the eastern Qinghai-Tibet plateau to its varied geography. Introduction The eared-pheasant genus Crossoptilon is endemic to China and includes four species. The Brown Eared-pheasant C. mantchuricum is found in northern China and the Blue Eared-pheasant C. auritum occurs on the plateau of northern Qinghai-Tibet. These species show no morphological variation and have no described subspecies. The White Eared-pheasant C. crossoptilon shows greater variations in plumage colour and four subspecies have been recognised: crossopti- lon in western Sichuan and south-eastern Tibet, lichiangense in north-western Yunnan, drouyni in the area between the Nujiang River and the Jinsha River, and dolani in Yushu of southern Qinghai. The Tibetan Eared-pheasant C. harmani is restricted to Tibet, north of the main axis of the Himalayas (Ludlow and Kinnear 1944). It was formerly treated as a subspecies of the White Eared-pheasant (Delacour 1977, Cheng et al. 1978), but more recently has been considered a full species (Sibley and Monroe 1990, Cheng 1994), mainly because of its dark blue- grey plumage, which is distinct from the predominately white plumage of the other subspecies. -
(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. -
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.