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Elegant Trogon (Trogon Elegans)
Elegant Trogon (Trogon elegans) NMPIF level: Biodiversity Conservation Concern, Level 1 (BC1) NMPIF assessment score: 16 NM stewardship responsibility: Low National PIF status: Watch List New Mexico BCRs: 34 Primary breeding habitat(s): Southwest Riparian Other habitats used: Madrean Pine-Oak Woodland (foraging) Summary of Concern Elegant Trogon is primarily a Mexican species with a limited breeding population in several mountain ranges of southeast Arizona, with at most a few pair breeding regularly in the Peloncillo Mountains of New Mexico. It requires moist riparian canyons with a sycamore component and upland areas of arid woodland. Associated Species Zone-tailed Hawk, Elf Owl (SC1), Black-chinned Hummingbird (SC2), Arizona Woodpecker (BC2), Northern Flicker, Dusky-capped Flycatcher, Hepatic Tanager, Brown-crested Flycatcher, Magnificent Hummingbird (BC2) Distribution Elegant Trogon is resident along the Pacific slope of Mexico from Sonora to Oaxaca, and in eastern Mexico from central Tamaulipas and southeast Nuevo León south to Puebla and Oaxaca (Howell and Webb 1995). A separate population is also resident in portions of Guatemala, El Salvador, and the interior of Honduras, south to Costa Rica. In summer, the breeding range extends a fairly short distance north into southeast Arizona. In New Mexico, this species is present only in the Peloncillo Mountains in southwest Hidalgo County (Kunzmann et al. 1998, Parmeter et al. 2002). Ecology and Habitat Requirements Across its range in Mexico and Central America, Elegant Trogon occupies a range of lowland, foothill and mountain habitats, including high elevation montane forests, semi-arid pine-oak woodland, lowland tropical deciduous forest and thorn forest. In southeast Arizona, where breeding populations have been studied, it is associated with sycamore- or high-elevation cottonwood-dominated riparian vegetation in a surrounding matrix of pinyon-juniper, pine-oak woodland or upland forest (Kunzmann et al. -
Foraging Flight Distances of Wintering Ducks and Geese: a Review
VOLUME 9, ISSUE 2, ARTICLE 2 Johnson, W. P., P. M. Schmidt, and D. P. Taylor. 2014. Foraging flight distances of wintering ducks and geese: a review. Avian Conservation and Ecology 9(2): 2. http://dx.doi.org/10.5751/ACE-00683-090202 Copyright © 2014 by the author(s). Published here under license by the Resilience Alliance. Research Paper Foraging flight distances of wintering ducks and geese: a review William P. Johnson 1, Paige M. Schmidt 1 and Dustin P. Taylor 2 1U.S. Fish and Wildlife Service, National Wildlife Refuge System, Division of Biological Sciences, 2U.S. Fish and Wildlife Service, Sequoyah National Wildlife Refuge ABSTRACT. The distance covered by foraging animals, especially those that radiate from a central area when foraging, may affect ecosystem, community, and population dynamics, and has conservation and landscape planning implications for multiple taxa, including migratory waterfowl. Migrating and wintering waterfowl make regular foraging flights between roosting and feeding areas that can greatly impact energetic resources within the foraging zone near roost sites. We reviewed published studies and gray literature for one- way foraging flight distances (FFDs) of migrating and wintering dabbling ducks and geese. Thirty reviewed studies reported FFDs and several reported values for multiple species or locations. We obtained FFD values for migration (n = 7) and winter (n = 70). We evaluated the effects of body mass, guild, i.e., dabbling duck or goose, and location, i.e., Nearctic or Palearctic, on FFDs. We used the second-order Akaike’s Information Criterion for model selection. We found support for effects of location and guild on FFDs. -
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. -
BIRDS of HALIMUN-SALAK NATIONAL PARK, WEST JAVA, INDONESIA: Saitou, N
Treubia 43: 31–46, December 2016 Treubia 43: 47–70, December 2016 BIRDS OF HALIMUN-SALAK NATIONAL PARK, WEST JAVA, INDONESIA: Saitou, N. & M. Nei 1987. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Molecular Biology and Evolution, 4: 406-425. ENDEMISM, CONSERVATION AND THREATENED STATUS Simmons, N.B. 2005. Order Chiroptera. In: Wilson, D.E. & D.M. Reeder (eds.). Mammal Species of the Dewi M. Prawiradilaga World: A Taxonomic and Geographic Reference. Baltimore: John Hopkins University Press. pp. 312- Museum Zoologicum Bogoriense, Research Center for Biology, Indonesian Institute of Sciences (LIPI) 529. Jl. Raya Jakarta-Bogor Km 46 Cibinong 16911, Indonesia e-mail: [email protected] Suyanto, A. 2001. Kelelawar di Indonesia. Bogor: Lembaga Ilmu Pengetahuan Indonesia. 126 pp. Temminck, C.J. 1827 (1824)-1841. Monographies de Mammalogie, ou description de quelques genres de Received: 8 August 2016; Accepted: 5 December 2016 mammiferes, dont les espèces ont été observées dans les différens musées de l’Europe. C.C. Vander Hoek, Leiden, 392 pp. ABSTRACT Thompson, J.D., T.J. Gibson & F. Plewniak 1997. The Clustal X Windows Interface: Flexible Strategies for Multiple Sequence Alignment Aided by the Quality Analysis Tools. Nucleic Acids Research, 24: Bird surveys and long-term bird monitoring in Gunung Halimun-Salak National Park were 4876-4882. conducted between 1998 and 2009 to obtain comprehensive data on the bird species in the area. Compilation of bird data from this study and other studies have recorded a total of 271 species, which is about 53.4% of van Strien, N.J. 1986. Abbreviated checklist of the mammals of the Australian Archipelago. -
Life History of the Black-Throated Trogon
LIFE HISTORY OF THE BLACK-THROATED TROGON BY ALEXANDER F. SKUTCH N Barro Colorado Island in Gatlin Lake, in the middle of the Isthmus of 0 Panama, I found my first twTo nests of the Black-throated Trogon (Trogon rufus) , in 1935. Both were destroyed by predators before the eggs hatched. Four years later, in the Valley of El General in southern Costa Rica, I found my third nest, which met a similar fate. In most of the succeeding years I have studied birds in the same region, where these trogons are not uncommon, and I have encountered five additional nests. With the exception of one which I did not see until the young were almost feathered, only the last was successful. This was situated on our farm in El General in April, 1958, and enabled me to round out a study begun 23 years earlier. The present paper is, then, a report of observations gathered over nearly a quarter of a century. The slowness of their accumulation is to be attributed to the diffi- culty of finding the nests of the majority of the birds that dwell in tropical rain-forest, and the discouragingly small proportion of these nests that yield living young. APPEARANCE AND RANGE One of the smaller members of its family, the Black-throated Trogon has a total length of about nine inches, of which well over half is accounted for by its long tail. The males’ predominant color is bright metallic green, which covers all the upper surface of head and body and likewise the chest. -
Northern Shoveler Anas Clypeata
Northern Shoveler Anas clypeata Folk Name: Spoonbill, Broad-bill, Spoon Bill Teal Status: Migrant, Winter Resident/Visitor Abundance: Uncommon Habitat: Lakes, ponds Take one good look at a Northern Shoveler and you will quickly realize how it acquired its various common names. Its large, conspicuous, spoon-shaped bill is unlike the bill of any other duck in the Carolinas. When viewed from above, the bill appears a bit like a shoe horn, narrow at the base and flaring out widely towards its rounded end, which can be a tad wider than the duck’s head. The shoveler is a heavy-bodied dabbling duck related to our teal ducks, but at 19 inches long, it is 3 ½ inches bigger reported one at Cowan’s Ford Wildlife Refuge on the than the Blue-winged and 5 inches bigger than the Green- very early date of 7 August in 1988, and one was reported winged Teal. Like our other dabbling ducks, it prefers lingering in Charlotte on April 28, 2012. Usually fewer shallow waters for foraging but any size pond will do. than 10 birds are seen at a time; however, an impressive In 1909, T. G. Pearson shared this assessment of the total of 948 was counted at Pee Dee NWR on January 2, Northern Shoveler with readers of the Greensboro Daily 2010. Historically, this duck was more common in the News: region during migration, but many mid-winter reports have been received since the turn of the twenty-first The male shoveler is a striking bird and the green century. of his head often leads the hasty observer at a Mary Akers, a 12-year-old bird watcher in Charlotte, distance to believe that he is looking at a mallard, shared this story of a weekend encounter with a “Spoon the similarity also being heightened in part by the Bill Teal,” in 1940: large size of the bird. -
Waterfowl in Iowa, Overview
STATE OF IOWA 1977 WATERFOWL IN IOWA By JACK W MUSGROVE Director DIVISION OF MUSEUM AND ARCHIVES STATE HISTORICAL DEPARTMENT and MARY R MUSGROVE Illustrated by MAYNARD F REECE Printed for STATE CONSERVATION COMMISSION DES MOINES, IOWA Copyright 1943 Copyright 1947 Copyright 1953 Copyright 1961 Copyright 1977 Published by the STATE OF IOWA Des Moines Fifth Edition FOREWORD Since the origin of man the migratory flight of waterfowl has fired his imagination. Undoubtedly the hungry caveman, as he watched wave after wave of ducks and geese pass overhead, felt a thrill, and his dull brain questioned, “Whither and why?” The same age - old attraction each spring and fall turns thousands of faces skyward when flocks of Canada geese fly over. In historic times Iowa was the nesting ground of countless flocks of ducks, geese, and swans. Much of the marshland that was their home has been tiled and has disappeared under the corn planter. However, this state is still the summer home of many species, and restoration of various areas is annually increasing the number. Iowa is more important as a cafeteria for the ducks on their semiannual flights than as a nesting ground, and multitudes of them stop in this state to feed and grow fat on waste grain. The interest in waterfowl may be observed each spring during the blue and snow goose flight along the Missouri River, where thousands of spectators gather to watch the flight. There are many bird study clubs in the state with large memberships, as well as hundreds of unaffiliated ornithologists who spend much of their leisure time observing birds. -
Breeding the Turquoise Tanager
Breeding the The Collared Turquoise Tanager Aracari by Jerry Jennings Fallbrook, California by Maarten de Ruiter Cambron Casteau, Belgium he Collared Aracari Pteroglossus T torquatus is a colorful native of Central America, ranging from southern ~e Turquoise Tanager Tanagara enclosure that could be heated. The Mexico south all the way to Colombia, ~cana is distributed from artificial light source within the in 1- and as such is the most common ofthe Venezuela over western Amazonia to door enclosure was turned on from Central American toucans to be encoun southeast Brazil. It is not found in 6:00 a.m. to 9:00 p.m. Along with the tered in the wild. Mexico as its scientific name suggests. Turquoise Tanagers were a pair of Though the Collared Aracari is com Itlives up to 500 meters (1600 feet) in Pekin Robins and two Bay-headed mon in the wild, it has been quite rare elevation and is seeninsmall groups of Tanagers. in captivity until the Fall of 1994, when up to six individual birds. There are The two Turquoise Tanagers were a few dozen birds were imported from five subspecies ofTurquoise Tanager, T. observed together most of the time Nicaragua. Prior to these importations, m. mexicana, T. m. vieilloti, T. m. media, and in the early part ofJune two eggs less than a dozen individuals were T. m. bolivicina and T. m. brasiliensis. were found in a small nest box. The known to exist in the U.S., and in just In Europe the Turquoise Tanager nest box measured 7 em x 7 em x 15 two collections, where they were repro is frequently available andthe subspe em high (2% in. -
13.3.3. Aquatic Invertebrates Important for Waterfowl Production
WATERFOWL MANAGEMENT HANDBOOK 13.3.3. Aquatic Invertebrates Important for Waterfowl Production Jan Eldridge that wetland. For example, invertebrates such as Bell Museum of Natural History leeches, earthworms, zooplankton, amphipods, University of Minnesota isopods, and gastropods are dependent on passive Minneapolis, MN 55455 dispersal (they can’t leave the wetland under their own power). As a result, they have elaborate mecha- Aquatic invertebrates play a critical role in the nisms to deal with drought and freezing. A second diet of female ducks during the breeding season. group that includes some beetles and most midges Most waterfowl hens shift from a winter diet of can withstand drought and freezing but requires seeds and plant material to a spring diet of mainly water to lay eggs in spring. A third group that in- invertebrates. The purpose of this chapter is to give cludes dragonflies, mosquitoes, and phantom managers a quick reference to the important inver- midges lays eggs in the moist mud of drying wet- tebrate groups that prairie-nesting ducks consume. lands during summer. A fourth group that includes Waterfowl species depend differentially on the most aquatic bugs and some beetles cannot cope various groups of invertebrates present in prairie with drying and freezing, so,they leave shallow wet- wetlands, but a few generalizations are possible. lands to overwinter in larger bodies of water. Man- agers can use the presence of these invertebrates to Snails, crustaceans, and insects are important inver- determine the effectiveness of water management tebrate groups for reproducing ducks (Table). Most regimes designed for waterfowl production. species of laying hens rely on calcium from snail The following descriptions of invertebrate natu- shells for egg production. -
Systematic Notes on Asian Birds. 38. the Mcclelland Drawings and a Reappraisal of the 1835-36 Survey of the Birds of Assam
ZV-344 063-106 | 38 05-01-2007 07:48 Page 63 Systematic notes on Asian birds. 38. The McClelland drawings and a reappraisal of the 1835-36 survey of the birds of Assam E.C. Dickinson With an Appendix by M.P. Walters Dickinson, E.C. Systematic notes on Asian birds. 38. The McClelland drawings and a reappraisal of the 1835-36 survey of the birds of Assam. Zool. Verh. Leiden 344, 12.ix.2003: 63-106, figs 1-4.— ISSN 0024-1652/ISBN 90-73239-88-5. Edward C. Dickinson, c/o The Trust for Oriental Ornithology, Flat 3, Bolsover Court, 19 Bolsover Road, Eastbourne, East Sussex, BN20 7JG, U.K. (e-mail: [email protected]). Keywords: McClelland; Horsfield; drawings; birds; Assam; history; British Library; Melanochlora; neo- type; Tesia olivea. McClelland brought back specimens and drawings from a survey in 1835-36 (and perhaps 1836-37). New birds were described in a paper read by Horsfield (1840). A comparison of the McClelland draw- ings of birds, held at the British Library, with the type specimens of birds newly named in 1840 and with other material has shown that McClelland’s collection was not fully reported. McClelland actually recorded about 170 species not just 96 as then listed. Some birds listed in 1840 were misidentified, of these some have been corrected earlier but at least one is here newly considered and looks as if it needs further correction. Taxonomic and nomenclatural notes are included when necessary. The correct name to apply to the one species in the genus Melanochlora, the Sultan Tit, is not safely established but as dating is not proven the name in present usage is maintained for the sake of stability. -
Alpha Codes for 2168 Bird Species (And 113 Non-Species Taxa) in Accordance with the 62Nd AOU Supplement (2021), Sorted Taxonomically
Four-letter (English Name) and Six-letter (Scientific Name) Alpha Codes for 2168 Bird Species (and 113 Non-Species Taxa) in accordance with the 62nd AOU Supplement (2021), sorted taxonomically Prepared by Peter Pyle and David F. DeSante The Institute for Bird Populations www.birdpop.org ENGLISH NAME 4-LETTER CODE SCIENTIFIC NAME 6-LETTER CODE Highland Tinamou HITI Nothocercus bonapartei NOTBON Great Tinamou GRTI Tinamus major TINMAJ Little Tinamou LITI Crypturellus soui CRYSOU Thicket Tinamou THTI Crypturellus cinnamomeus CRYCIN Slaty-breasted Tinamou SBTI Crypturellus boucardi CRYBOU Choco Tinamou CHTI Crypturellus kerriae CRYKER White-faced Whistling-Duck WFWD Dendrocygna viduata DENVID Black-bellied Whistling-Duck BBWD Dendrocygna autumnalis DENAUT West Indian Whistling-Duck WIWD Dendrocygna arborea DENARB Fulvous Whistling-Duck FUWD Dendrocygna bicolor DENBIC Emperor Goose EMGO Anser canagicus ANSCAN Snow Goose SNGO Anser caerulescens ANSCAE + Lesser Snow Goose White-morph LSGW Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Intermediate-morph LSGI Anser caerulescens caerulescens ANSCCA + Lesser Snow Goose Blue-morph LSGB Anser caerulescens caerulescens ANSCCA + Greater Snow Goose White-morph GSGW Anser caerulescens atlantica ANSCAT + Greater Snow Goose Intermediate-morph GSGI Anser caerulescens atlantica ANSCAT + Greater Snow Goose Blue-morph GSGB Anser caerulescens atlantica ANSCAT + Snow X Ross's Goose Hybrid SRGH Anser caerulescens x rossii ANSCAR + Snow/Ross's Goose SRGO Anser caerulescens/rossii ANSCRO Ross's Goose -
2020 North Carolina Ornithology List
2020 North Carolina Ornithology List Kingdom – ANIMALIA Phylum – CHORDATA Key: Sub Phylum – VERTEBRATA Regional level (62 in total) Class – AVES Addition for State level (110 in total) Family Grou p (Family Name) Addition for National level (160 in total) Common Name [Scientific name is in italics] ORDER: Anseriformes Ibises and Spoonbills ORDER: Charadriiformes Ducks, Geese, and Swans (Anatidae) (Threskiornithidae) Lapwings and Plovers (Charadriidae) Northern Shoveler Roseate Spoonbill Platalea ajaja American Golden-Plover Green-winged Teal Killdeer Charadrius vociferus Canvasback ORDER: Suliformes Oystercatchers (Haematopodidae) Hooded Merganser Cormorants (Phalacrocoracidae) American Oystercatcher Black-bellied Whistling-Duck Double-crested Cormorant Stilts and Avocets (Recurvirostridae) Snow Goose Chen caerulescens Phalacrocorax auritus Black-necked Stilt Canada Goose Branta canadensis Darters (Anhingidae) American Avocet Recurvirostra Trumpeter Swan Anhinga Anhinga anhinga americana Wood Duck Aix sponsa Frigatebirds (Fregatidae) Sandpipers, Phalaropes, and Allies Mallard Anas platyrhynchos Magnificent Frigatebird (Scolopacidae) Cinnamon Teal Anas cyanoptera American Woodcock Scolopax minor ORDER: Ciconiiformes Spotted Sandpiper ORDER: Galliformes Deep-water Waders (Ciconiidae) Ruddy Turnstone Partridges, Grouse, Turkeys, and Old Wood stork Dunlin Calidris alpina World Quail Wilson’s Snipe (Phasianidae ) ORDER: Falconiformes Gulls, Terns, and Skimmers Ring-necked Pheasant Caracaras and Falcons (Falconidae) (Laridae) Ruffed Grouse