Bird Banding Manual, Vol. II
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Species Assessment for Sage Thrasher (Oreoscoptes Montanus) in Wyoming
SPECIES ASSESSMENT FOR SAGE THRASHER (OREOSCOPTES MONTANUS ) IN WYOMING prepared by 1 2 1 REBECCA S B USECK , DOUGLAS A. K EINATH , AND MATTHEW H. M CGEE 1 Wyoming Natural Diversity Database, University of Wyoming, 1000 E. University Ave, Dept. 3381, Laramie, Wyoming 82071; 307-766-3023 2 Zoology Program Manager, Wyoming Natural Diversity Database, University of Wyoming, 1000 E. University Ave, Dept. 3381, Laramie, Wyoming 82071; 307-766-3013; [email protected] prepared for United States Department of the Interior Bureau of Land Management Wyoming State Office Cheyenne, Wyoming December 2004 Buseck, Keinath, and McGee – Oreoscoptes montanus December 2004 Table of Contents SUMMARY .......................................................................................................................................... 3 INTRODUCTION ................................................................................................................................. 3 NATURAL HISTORY ........................................................................................................................... 4 Morphological Description ...................................................................................................... 4 Taxonomy and Distribution ..................................................................................................... 6 Habitat Requirements............................................................................................................. 8 General .............................................................................................................................................8 -
Recommended English Names
86 BIRDS OF THE WORLD: RECOMMENDED ENGLISH NAMES Gill, F.B. & Wright, M. 2006. Princeton, NJ, and London, UK: Princeton University Press. 259 pp. with CD containing Microsoft Excel spreadsheets of species lists. Soft cover. ISBN 0691128278. US$20. Birds are among the few taxa for which non-scientific vernacular In addition to competing English names, the IOC committee had names are extensively used in scientific communication as well to deal with ongoing taxonomic shuffling too. It isn’t clear how as in the burgeoning birding community. Consequently, there is a they reached consensus here, but some recent splits are recognized need to have some consistency in the names used around the world. (e.g. Nazca Booby, Vega Gull, the various sub-Antarctic shags), and The International Ornithological Congress (IOC) sought to reach others are not (e.g. the suggested splits of Wandering, Yellow-nosed consensus in vernacular names for commonly used languages. and other albatrosses). As the editors reiterate, this compilation is a Standardized names have been published for French (Devillers work in progress, and future versions will undoubtedly address the and Ouellet 1993) and Spanish (Bernis 1995). The goal of Birds changing taxonomic landscape. of the World: Recommended English Names is to promote a set of unique English names for the extant bird species of the world. Led Everyone who peruses these lists will be disappointed to see some old originally by the now-late Burt Monroe, and then Frank Gill and favourites voted out and will find fault with some decisions (I think I Minturn Wright, an IOC committee and regional subcommittees hear the rumble of European dissent over their guillemots and divers). -
The Relationships of the Starlings (Sturnidae: Sturnini) and the Mockingbirds (Sturnidae: Mimini)
THE RELATIONSHIPS OF THE STARLINGS (STURNIDAE: STURNINI) AND THE MOCKINGBIRDS (STURNIDAE: MIMINI) CHARLESG. SIBLEYAND JON E. AHLQUIST Departmentof Biologyand PeabodyMuseum of Natural History,Yale University, New Haven, Connecticut 06511 USA ABSTRACT.--OldWorld starlingshave been thought to be related to crowsand their allies, to weaverbirds, or to New World troupials. New World mockingbirdsand thrashershave usually been placed near the thrushesand/or wrens. DNA-DNA hybridization data indi- cated that starlingsand mockingbirdsare more closelyrelated to each other than either is to any other living taxon. Some avian systematistsdoubted this conclusion.Therefore, a more extensiveDNA hybridizationstudy was conducted,and a successfulsearch was made for other evidence of the relationshipbetween starlingsand mockingbirds.The resultssup- port our original conclusionthat the two groupsdiverged from a commonancestor in the late Oligoceneor early Miocene, about 23-28 million yearsago, and that their relationship may be expressedin our passerineclassification, based on DNA comparisons,by placing them as sistertribes in the Family Sturnidae,Superfamily Turdoidea, Parvorder Muscicapae, Suborder Passeres.Their next nearest relatives are the members of the Turdidae, including the typical thrushes,erithacine chats,and muscicapineflycatchers. Received 15 March 1983, acceptedI November1983. STARLINGS are confined to the Old World, dine thrushesinclude Turdus,Catharus, Hylocich- mockingbirdsand thrashersto the New World. la, Zootheraand Myadestes.d) Cinclusis -
Part 4 Appendices
Part 4 Appendices HEARD ISLAND AND MCDONALD ISLANDS MARINE RESERVE 139 Appendix 1. Proclamation of Heard Island and McDonald Islands Marine Reserve 140 MANAGEMENT PLAN HEARD ISLAND AND MCDONALD ISLANDS MARINE RESERVE 141 142 MANAGEMENT PLAN Appendix 2. Native Fauna of the HIMI Marine Reserve Listed Under the EPBC Act Scientific Name Common Name Birds recorded as breeding Aptenodytes patagonicus king penguin S Catharacta lonnbergi subantarctic skua S Daption capense cape petrel S Diomeda exulans wandering albatross V S M B J A Diomeda melanophrys black–browed albatross S M B A Eudyptes chrysocome southern rockhopper penguin S Eudyptes chrysolophus macaroni penguin S Larus dominicanus kelp gull S Macronectes giganteus southern giant petrel E S M B A Oceanites oceanicus Wilson’s storm petrel S M J Pachyptila crassirostris fulmar prion S Pachyptila desolata Antarctic prion S Pelecanoides georgicus South Georgian diving petrel S Pelecanoides urinatrix common diving petrel S Phalacrocorax atriceps (e) Heard Island cormorant V S Phoebetria palpebrata light mantled sooty albatross S M B A Pygoscelis papua gentoo penguin S Sterna vittata Antarctic tern V S Non–breeding birds Catharacta maccormicki south polar skua S M J Diomedea epomophora southern royal albatross V S M B A Fregetta grallaria white–bellied storm petrel S Fregetta tropica black–bellied storm petrel S Fulmarus glacialoides southern fulmar S Garrodia nereis grey–backed storm petrel S Halobaena caerulea blue petrel V S Macronectes halli northern giant petrel V S M B A Pachyptila belcheri -
Wildland Fire in Ecosystems: Effects of Fire on Fauna
United States Department of Agriculture Wildland Fire in Forest Service Rocky Mountain Ecosystems Research Station General Technical Report RMRS-GTR-42- volume 1 Effects of Fire on Fauna January 2000 Abstract _____________________________________ Smith, Jane Kapler, ed. 2000. Wildland fire in ecosystems: effects of fire on fauna. Gen. Tech. Rep. RMRS-GTR-42-vol. 1. Ogden, UT: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station. 83 p. Fires affect animals mainly through effects on their habitat. Fires often cause short-term increases in wildlife foods that contribute to increases in populations of some animals. These increases are moderated by the animals’ ability to thrive in the altered, often simplified, structure of the postfire environment. The extent of fire effects on animal communities generally depends on the extent of change in habitat structure and species composition caused by fire. Stand-replacement fires usually cause greater changes in the faunal communities of forests than in those of grasslands. Within forests, stand- replacement fires usually alter the animal community more dramatically than understory fires. Animal species are adapted to survive the pattern of fire frequency, season, size, severity, and uniformity that characterized their habitat in presettlement times. When fire frequency increases or decreases substantially or fire severity changes from presettlement patterns, habitat for many animal species declines. Keywords: fire effects, fire management, fire regime, habitat, succession, wildlife The volumes in “The Rainbow Series” will be published during the year 2000. To order, check the box or boxes below, fill in the address form, and send to the mailing address listed below. -
Appendix, French Names, Supplement
685 APPENDIX Part 1. Speciesreported from the A.O.U. Check-list area with insufficient evidencefor placementon the main list. Specieson this list havebeen reported (published) as occurring in the geographicarea coveredby this Check-list.However, their occurrenceis considered hypotheticalfor one of more of the following reasons: 1. Physicalevidence for their presence(e.g., specimen,photograph, video-tape, audio- recording)is lacking,of disputedorigin, or unknown.See the Prefacefor furtherdiscussion. 2. The naturaloccurrence (unrestrained by humans)of the speciesis disputed. 3. An introducedpopulation has failed to becomeestablished. 4. Inclusionin previouseditions of the Check-listwas basedexclusively on recordsfrom Greenland, which is now outside the A.O.U. Check-list area. Phoebastria irrorata (Salvin). Waved Albatross. Diornedeairrorata Salvin, 1883, Proc. Zool. Soc. London, p. 430. (Callao Bay, Peru.) This speciesbreeds on Hood Island in the Galapagosand on Isla de la Plata off Ecuador, and rangesat seaalong the coastsof Ecuadorand Peru. A specimenwas takenjust outside the North American area at Octavia Rocks, Colombia, near the Panama-Colombiaboundary (8 March 1941, R. C. Murphy). There are sight reportsfrom Panama,west of Pitias Bay, Dari6n, 26 February1941 (Ridgely 1976), and southwestof the Pearl Islands,27 September 1964. Also known as GalapagosAlbatross. ThalassarchechrysosWma (Forster). Gray-headed Albatross. Diornedeachrysostorna J. R. Forster,1785, M6m. Math. Phys. Acad. Sci. Paris 10: 571, pl. 14. (voisinagedu cerclepolaire antarctique & dansl'Ocean Pacifique= Isla de los Estados[= StatenIsland], off Tierra del Fuego.) This speciesbreeds on islandsoff CapeHorn, in the SouthAtlantic, in the southernIndian Ocean,and off New Zealand.Reports from Oregon(mouth of the ColumbiaRiver), California (coastnear Golden Gate), and Panama(Bay of Chiriqu0 are unsatisfactory(see A.O.U. -
Distribution, Ecology, and Life History of the Pearly-Eyed Thrasher (Margarops Fuscatus)
Adaptations of An Avian Supertramp: Distribution, Ecology, and Life History of the Pearly-Eyed Thrasher (Margarops fuscatus) Chapter 6: Survival and Dispersal The pearly-eyed thrasher has a wide geographical distribution, obtains regional and local abundance, and undergoes morphological plasticity on islands, especially at different elevations. It readily adapts to diverse habitats in noncompetitive situations. Its status as an avian supertramp becomes even more evident when one considers its proficiency in dispersing to and colonizing small, often sparsely The pearly-eye is a inhabited islands and disturbed habitats. long-lived species, Although rare in nature, an additional attribute of a supertramp would be a even for a tropical protracted lifetime once colonists become established. The pearly-eye possesses passerine. such an attribute. It is a long-lived species, even for a tropical passerine. This chapter treats adult thrasher survival, longevity, short- and long-range natal dispersal of the young, including the intrinsic and extrinsic characteristics of natal dispersers, and a comparison of the field techniques used in monitoring the spatiotemporal aspects of dispersal, e.g., observations, biotelemetry, and banding. Rounding out the chapter are some of the inherent and ecological factors influencing immature thrashers’ survival and dispersal, e.g., preferred habitat, diet, season, ectoparasites, and the effects of two major hurricanes, which resulted in food shortages following both disturbances. Annual Survival Rates (Rain-Forest Population) In the early 1990s, the tenet that tropical birds survive much longer than their north temperate counterparts, many of which are migratory, came into question (Karr et al. 1990). Whether or not the dogma can survive, however, awaits further empirical evidence from additional studies. -
Snowy Sheathbills and What You Really Need to Know
Snowy Sheathbills and what you really need to know Reprinted from British Antarctic Survey Bulletin, No. 2, December 1963, p. 53-71 THE SHEATHBILL, Chionis alba (Gmelin), AT SIGNY ISLAND, SOUTH ORKNEY ISLANDS By N. V. Jones ABSTRACT. A study of the sheathbill, Chionis alba (Gmelin), was carried out at Signy Island, South Orkney Islands, between April 1961 and April 1962. The general characteristics of the species and the annual population cycle have been investigated. Breeding birds return to the island early in October, form pairs early in November, and establish territories later in November. There is a high level of fidelity to a previous year's mate and considerable nest-site tenacity. Nests are concentrated around penguin (Pygoscelis adetiae and P. antarctica) colonies, the closer association being with the latter species. Both sexes participate in nest construction, incubation and the care of the chick. Egg-laying begins in early December, but full incubation starts only when clutches, which number from one to four, are complete. The normal incubation period is 30 days. Chicks are fed largely on "krill", obtained by disturbing penguins which are feeding their own young, and the sheathbill's life cycle is suitably coincident with that of the penguins. Chicks fledge when 50 to 60 days old and at this stage they become shore feeders. Chicks and adults disperse from the island in about mid-May, and there is evidence of a rather loose northward migration in winter. No definite predators are known. A number of parasites have been recorded. THIS paper describes work done on the sheathbill at Signy Island (lat. -
Penguin Island ANTARCTIC TREATY Penguin Island Visitor Site Guide 62˚06’S, 57˚54’W - Eastern King George Island
Penguin Island ANTARCTIC TREATY Penguin Island visitor site guide 62˚06’S, 57˚54’W - Eastern King George Island Key features King George Is. - Dormant volcanic cone Ferraz Station Turret Point - Southern Giant Petrels Admiralty Bay Elephant Is. Maxwell Bay PENGUIN ISLAND Marsh/frei Stations Great Wall Station - Chinstrap Penguins Bellingshausen Station Arctowski Station Artigas Station Jubany Station King Sejong Station - Vegetation Potter Cove Aitcho Islands Nelson Is. - Whale bones Robert Is. Mitchell Cove Greenwich Is. Robert Point Fort Point Half Moon Is. Yankee Harbour Description Livingston Is. TOPOGRAPHY This oval island is 1.6km long. The site’s prominent geological feature is the 170m high cone of Deacon Hannah Point Bransfield Strait Peak, the northernSnow face Is. of which slopes gently down to the landing beach. Most of the island is surrounded by low cliffs, and thereTelefon is a crater lake in the northeast. Bay Pendulum Cove Gourdin Is. FAUNA Confirmed breeders: ChinstrapDeception penguin Is. Pygoscelis( Baily Head antarctica), Adélie penguin (Pygoscelis adeliae), southern giant petrel (MacronectesVapour Col giganteus), Antarctic tern (Sterna vittata), kelp gull (Larus Cape Whaler's Bay Dubouzet dominicanus), and skuas (Catharacta spp.). Likely breeders: Snowy sheathbill (Chionis alba) B.and O'higgins Wilson’s Station storm petrel (Oceanites oceanicus). Regular roosting: blue-eyed shags (AstrPhalacrocoraxolabe atriceps). RegularlyCape Hope Legoupil haul out: Southern elephant seals (Mirounga leonina) and Weddell seals (IslandLeptonychotes weddellii). Bay a FLORA Deschampsia antarctica, Colobanthus quitensis, Xanthoria elegans, moss species, Caloplaca and otherinsul crustose lichen species, and large swards of the fruticose lichen Usnea antarctica. Pen inity Northwest (Nw) Tr Subarea Bone Bay Visitor Impact Tower Is. -
SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does Not Include Alcidae
SHOREBIRDS (Charadriiformes*) CARE MANUAL *Does not include Alcidae CREATED BY AZA CHARADRIIFORMES TAXON ADVISORY GROUP IN ASSOCIATION WITH AZA ANIMAL WELFARE COMMITTEE Shorebirds (Charadriiformes) Care Manual Shorebirds (Charadriiformes) Care Manual Published by the Association of Zoos and Aquariums in association with the AZA Animal Welfare Committee Formal Citation: AZA Charadriiformes Taxon Advisory Group. (2014). Shorebirds (Charadriiformes) Care Manual. Silver Spring, MD: Association of Zoos and Aquariums. Original Completion Date: October 2013 Authors and Significant Contributors: Aimee Greenebaum: AZA Charadriiformes TAG Vice Chair, Monterey Bay Aquarium, USA Alex Waier: Milwaukee County Zoo, USA Carol Hendrickson: Birmingham Zoo, USA Cindy Pinger: AZA Charadriiformes TAG Chair, Birmingham Zoo, USA CJ McCarty: Oregon Coast Aquarium, USA Heidi Cline: Alaska SeaLife Center, USA Jamie Ries: Central Park Zoo, USA Joe Barkowski: Sedgwick County Zoo, USA Kim Wanders: Monterey Bay Aquarium, USA Mary Carlson: Charadriiformes Program Advisor, Seattle Aquarium, USA Sara Perry: Seattle Aquarium, USA Sara Crook-Martin: Buttonwood Park Zoo, USA Shana R. Lavin, Ph.D.,Wildlife Nutrition Fellow University of Florida, Dept. of Animal Sciences , Walt Disney World Animal Programs Dr. Stephanie McCain: AZA Charadriiformes TAG Veterinarian Advisor, DVM, Birmingham Zoo, USA Phil King: Assiniboine Park Zoo, Canada Reviewers: Dr. Mike Murray (Monterey Bay Aquarium, USA) John C. Anderson (Seattle Aquarium volunteer) Kristina Neuman (Point Blue Conservation Science) Sarah Saunders (Conservation Biology Graduate Program,University of Minnesota) AZA Staff Editors: Maya Seaman, MS, Animal Care Manual Editing Consultant Candice Dorsey, PhD, Director of Animal Programs Debborah Luke, PhD, Vice President, Conservation & Science Cover Photo Credits: Jeff Pribble Disclaimer: This manual presents a compilation of knowledge provided by recognized animal experts based on the current science, practice, and technology of animal management. -
Attempting to See One Member of Each of the World's Bird Families Has
Attempting to see one member of each of the world’s bird families has become an increasingly popular pursuit among birders. Given that we share that aim, the two of us got together and designed what we believe is the most efficient strategy to pursue this goal. Editor’s note: Generally, the scientific names for families (e.g., Vireonidae) are capital- ized, while the English names for families (e.g., vireos) are not. In this article, however, the English names of families are capitalized for ease of recognition. The ampersand (&) is used only within the name of a family (e.g., Guans, Chachalacas, & Curassows). 8 Birder’s Guide to Listing & Taxonomy | October 2016 Sam Keith Woods Ecuador Quito, [email protected] Barnes Hualien, Taiwan [email protected] here are 234 extant bird families recognized by the eBird/ Clements checklist (2015, version 2015), which is the offi- T cial taxonomy for world lists submitted to ABA’s Listing Cen- tral. The other major taxonomic authority, the IOC World Bird List (version 5.1, 2015), lists 238 families (for differences, see Appendix 1 in the expanded online edition). While these totals may appear daunting, increasing numbers of birders are managing to see them all. In reality, save for the considerable time and money required, finding a single member of each family is mostly straightforward. In general, where family totals or family names are mentioned below, we use the eBird/Clements taxonomy unless otherwise stated. Family Feuds: How do world regions compare? In descending order, the number of bird families supported by con- tinental region are: Asia (125 Clements/124 IOC), Africa (122 Clem- ents/126 IOC), Australasia (110 Clements/112 IOC), North America (103 Clements/IOC), South America (93 Clements/94 IOC), Europe (73 Clements/74 IOC ), and Antarctica (7 Clements/IOC). -
Appendix from R. E. Ricklefs and E. Bermingham, “The Causes of Evolutionary Radiations in Archipelagoes: Passerine Birds in the Lesser Antilles” (Am
᭧ 2007 by The University of Chicago. All rights reserved. Appendix from R. E. Ricklefs and E. Bermingham, “The Causes of Evolutionary Radiations in Archipelagoes: Passerine Birds in the Lesser Antilles” (Am. Nat., vol. 169, no. 3, p. 000) Additional Supporting Materials Species of Passerine Birds on the Archipelagoes Hawaiian Islands (based on Pratt 1979; Berger 1981; James and Olson 1991): (1) Corvus hawaiiensis (Corvidae, one species), (2) Myadestes thrushes (Turdinae, five species [two sympatric]), (3) Acrocephalus familiaris (Acrocephalinae, one species), (4) Chasiempsis sandwichensis (Monarchini, one species), (5) Hawaiian Oo and Kioea (Meliphagidae, five species [two sympatric]), and (6) Hawaiian honeycreepers (Drepanidini, 35 species, 22 extant, plus many fossil taxa). Gala´pagos Islands (Harris 1973): (1) Pyrocephalus rubinus (Tyrannidae), (2) Myiarchus magnirostris (Tyrannidae), (3) Progne modesta (Hirundinidae), (4) Nesomimus mockingbirds (Mimidae, four allopatric species), (5) Dendroica petechia (Parulinae), and (6) Darwin’s finches (Thraupini, 13 species). New Hebrides: Species numbered 33–56 in the systematic list of Diamond and Marshall (1976, app. 1), all of which represent independent colonizations: (1) Hirundo tahitica,(2)Lalage maculosa,(3)Lalage leucopyga,(4) Coracina caledonica,(5)Turdus poliocephalus,(6)Cichlornis whitneyi,(7)Gerygone flavolateralis,(8) Rhipidura spilodera,(9)Rhipidura fuliginosa, (10) Myiagra caledonica, (11) Neolalage banksiana, (12) Clytorhynchus pachycephaloides, (13) Petroica multicolor, (14) Pachecephala