Australian National Directory of Important Migratory Shorebird Habitat
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Resource Partitioning by Wintering Shorebirds : a Behavioral Comparison of Two Species in a Tropical Estuary
UC Berkeley Student Research Papers, Fall 2006 Title Resource Partitioning By Wintering Shorebirds : A Behavioral Comparison of Two Species in a Tropical Estuary Permalink https://escholarship.org/uc/item/3fb344vf Author Greene, Andrew D. Publication Date 2006-12-01 eScholarship.org Powered by the California Digital Library University of California RESOURCE PARTITIONING BY WINTERING SHOREBIRDS: A BEHAVIORAL COMPARISON OF TWO SPECIES IN A TROPICAL ESTUARY ANDREW D. GREENE Environmental Science Policy and Management, University of California, Berkeley, California 94720 USA Abstract. Shorebirds often feed in multispecies groups that display interesting niche dynamics. On Moorea, French Polynesia, the Wandering Tattler (Tringa incana) and Pacific Golden Plover (Pluvialis fulva) are the dominant shorebird species during the northern winter. These species’ feeding behavior was observed at the Temae estuary on the northeast side of the island. Relative abundance of the two species was determined using transect counts at the estuary and an adjacent beach. T. incana displayed more striking and sprinting behavior, while P. fulva displayed more picking and walking behavior. T. incana also consumed more crabs than P. fulva. The two species existed in relatively equal abundance in the estuary; T. incana was more common on the beach. Though these data suggest some differences in feeding niche, a great deal of overlap was observed. The degree of niche partitioning appears to be greater in this study than in similar studies conducted on these species’ breeding grounds. Key words: feeding behavior; Pluvialis fulva; Tringa incana; Moorea, French Polynesia; resource partitioning; estuary INTRODUCTION spatial distribution of each bird species’ preferred prey (Ribeiro et al. -
THE EUPHONIA Quarterly Journal of Mexican Avifauna Volume 1, Number 2 December 1992 the EUPHONIA Quarterly Journal of Mexican Avifauna
THE EUPHONIA Quarterly Journal of Mexican Avifauna Volume 1, Number 2 December 1992 THE EUPHONIA Quarterly Journal of Mexican Avifauna Editor: Kurt Radamaker Associate Editors: Michael A. Patten, Deb Davidson Spanish Consultant: Luis Santaella Consultant: Steve N.G. Howell Proofreaders: Richard A. Erickson, Bob Pann Circulation Manager: Cindy Ludden For an annual subscription to The Euphonia, please send 15.00 dollars U.S. payable to The Euphonia P.O. Box 8045, Santa Maria, California, 93456-8045, U.S.A. Checks drawn on Bancomer in Pesos accepted. The Euphonia encourages you to send in manuscripts. Appropriate topics range from recent sightings to scientific studies of Mexican birds. Feature articles in Spanish are encouraged. Please send manuscripts, preferably on diskette written in Wordperfect (although almost any major word processor file will suffice), to Kurt Radamaker, P.O. Box 8045, Santa Maria, California 93456, U.S.A. Please send summaries for Recent Ornithological Literature to Michael A. Patten at P.O. Box 8561, Riverside, California, 92515-8561, U.S.A. Recent sightings (with details) should be sent to Luis Santaella, 919 Second St., Encinitas, California 92024, U.S.A. Contents 27 OBSERVATIONS OF NORTH AMERICAN MIGRANT BIRDS IN THE REVILLAGIGEDO ISLANDS Steve N.G. Howell and Sophie Webb 34 PARASITISM OF YELLOW-OLIVE FLY CATCHER BY THE PHEASANT CUCKOO Richard G. Wilson 37 SEMIPALMATED SANDPIPER RECORDS FOR BAJA CALIFORNIA Thomas E. Wurster and Kurt Radamaker 39 RECENT RECORDS OF MAROON-CHESTED GROUND-DOVE IN MEXICO Steve N.G. Howell 42 OBSERVATION OF A BENDIRE'S THRASHER FROM NORTHEAST BAJA CALIFORNIA Brian Daniels, Doug Willick and Thomas E. -
Draft Version Target Shorebird Species List
Draft Version Target Shorebird Species List The target species list (species to be surveyed) should not change over the course of the study, therefore determining the target species list is an important project design task. Because waterbirds, including shorebirds, can occur in very high numbers in a census area, it is often not possible to count all species without compromising the quality of the survey data. For the basic shorebird census program (protocol 1), we recommend counting all shorebirds (sub-Order Charadrii), all raptors (hawks, falcons, owls, etc.), Common Ravens, and American Crows. This list of species is available on our field data forms, which can be downloaded from this site, and as a drop-down list on our online data entry form. If a very rare species occurs on a shorebird area survey, the species will need to be submitted with good documentation as a narrative note with the survey data. Project goals that could preclude counting all species include surveys designed to search for color-marked birds or post- breeding season counts of age-classed bird to obtain age ratios for a species. When conducting a census, you should identify as many of the shorebirds as possible to species; sometimes, however, this is not possible. For example, dowitchers often cannot be separated under censuses conditions, and at a distance or under poor lighting, it may not be possible to distinguish some species such as small Calidris sandpipers. We have provided codes for species combinations that commonly are reported on censuses. Combined codes are still species-specific and you should use the code that provides as much information as possible about the potential species combination you designate. -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
Update on the Birds of Isla Guadalupe, Baja California
UPDATE ON THE BIRDS OF ISLA GUADALUPE, BAJA CALIFORNIA LORENZO QUINTANA-BARRIOS and GORGONIO RUIZ-CAMPOS, Facultad de Ciencias, Universidad Autónoma de Baja California, Apartado Postal 1653, Ense- nada, Baja California, 22800, México (U. S. mailing address: PMB 064, P. O. Box 189003, Coronado, California 92178-9003; [email protected] PHILIP UNITT, San Diego Natural History Museum, P. O. Box 121390, San Diego, California 92112-1390; [email protected] RICHARD A. ERICKSON, LSA Associates, 20 Executive Park, Suite 200, Irvine, California 92614; [email protected] ABSTRACT: We report 56 bird specimens of 31 species taken on Isla Guadalupe, Baja California, between 1986 and 2004 and housed at the Colección Ornitológica del Laboratorio de Vertebrados de la Facultad de Ciencias, Universidad Autónoma de Baja California, Ensenada, along with other sight and specimen records. The speci- mens include the first published Guadalupe records for 10 species: the Ring-necked Duck (Aythya collaris), Long-billed Curlew (Numenius americanus), Bonaparte’s Gull (Larus philadelphia), Ash-throated Flycatcher (Myiarchus cinerascens), Warbling Vireo (Vireo gilvus), Tree Swallow (Tachycineta bicolor), Yellow Warbler (Dendroica petechia), Magnolia Warbler (Dendroica magnolia), Yellow-headed Blackbird (Xan- thocephalus xanthocephalus), and Orchard Oriole (Icterus spurius). A specimen of the eastern subspecies of Brown-headed Cowbird (Molothrus ater ater) and a sight record of the Gray-cheeked Thrush (Catharus minimus) are the first reported from the Baja California Peninsula (and islands). A photographed Franklin’s Gull (Larus pipixcan) is also an island first. Currently 136 native species and three species intro- duced in North America have been recorded from the island and nearby waters. -
Field Notes on the Grey-Tailed Tattler
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Keast, J. A., 1949. Field notes on the grey-tailed tattler. Records of the Australian Museum 22(2): 207–211. [18 January 1949]. doi:10.3853/j.0067-1975.22.1949.601 ISSN 0067-1975 Published by the Australian Museum, Sydney nature culture discover Australian Museum science is freely accessible online at http://publications.australianmuseum.net.au 6 College Street, Sydney NSW 2010, Australia FIELD NOTES ON THE GREY-TAILED TATTLER. By J. A. KEAST. The Australian Museum, Sydney. Habitat-preference amongst the migratory Charadriiformes is an aspect of study to which little attention has been paid in Australia. That these hardy and resolute birds, which bj-annually traverse half the world, should have reached a high stage of adaptability would appear certain. It is therefore surprising to find that some species restrict themselves in their choice of feeding grounds, a differential distribution that has led to a concept of rarity in the case of some comparatively common visitors. Such is the case as regards the Grey-tailed Tattler (Tringa brevipes) in New South Wales, as has been shown by observations made during recent years. The Official Checklist of the Birds of Au.stralia (1926) gives the range of the Grey-tailed Tattler in Australia as "Northern Australia, South Queensland, and Western Australia". Actually the species was known from Sydney a quarter of a century previous to this (North, 1898), but it was not until K. A. Hindwood made frequent observations at Long Reef, a rocky promontory near -Collaroy, that the species was shown to be a regular summer inhabitant of coastal New South Wales. -
The Sanderling on Wilson's Promontory by Roy P
Vol. 3 OCTOBER 31, 1970 No.8 The Sanderling on Wilson's Promontory by Roy P. Cooper*, Melbourne Although overseas books on ornithology have described the Sanderling, Calidris alba, as being "common on almost every ocean beach in the world", this does not apply, from the published records, to Australia. On this continent they are classed as rare species and they appear to return each year to a favourite area, where they may be seen in small flocks varying from five to two hundred birds. The main areas are at Boat Harbour, south of Sydney; several places from Port Phillip to Portland, in western Victoria : Goolwa Beach (200 birds) and at Pondalowie Bay in South Australia; also recorded in Western Australia and in Queensland. In the Australian Bird W ate her, 3:243, some of the observations recorded by the team who is carrying out the Survey of the Birds of Wilson's Promontory, were published, revealing the occurrence of the Sanderling in that area; the first records for eastern Victoria. This distribution is somewhat similar to that of the nesting groups. An Arctic breeder, the Sanderling nests within the Arctic Circle, in the tundra climatic zone. Although this zone extends around the Arctic Ocean, in northern Canada, Greenland, Europe and Asia, and the bird nests "within a mile or two of the coast", it appears to breed in very selected areas, and there are large gaps between the groups. It breeds on some of the Arctic islands of Canada; also along the north-western and north-eastern coasts of Greenland; in Spitsbergen; and in Siberia on Taymyr Peninsula, New Siberian Islands and Liakof Island. -
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. -
Peeps and Related Sandpipers Peeps Are a Group of Diminutive Sandpipers That Are Notoriously Hard to Tell Apart
Peeps and Related Sandpipers Peeps are a group of diminutive sandpipers that are notoriously hard to tell apart. They belong to a subfamily of subarctic and arctic nesting sandpipers known as the Calidridinae (in the sandpiper family, Scolopacidae). During their migrations, when most residents of North America have the opportunity to watch them, mixed flocks of calidridine sandpipers scurry about on mudflats, feeding at the edge of the retreating tide, or swarm aloft, twisting and turning like a dense school of fish. These traits, in a group of birds that look so much alike to start with, give bird watchers nightmares. Fortunately for Alaskans and visitors to our state, Alaska is an excellent location to view and identify calidridine sandpipers. The early summer breeding season is the easiest time of the year to distinguish the various species, not only because they are in breeding plumage and are more approachable than at other times of the year, but also because each species performs a characteristic courtship display with unique vocalizations. For the avid birder, Alaska has the additional attraction of being one of the best places in North America to view exotic Eurasian species. General description: Three peeps are abundant summer residents and breeders in Alaska—the least, semipalmated, and western sandpipers (Calidris minutilla, C. pusilla, and C. mauri) [all lists in order by size]. Another four species from Eurasia may also be seen—the little, rufous-necked, Temminck's, and long-toed stints (“stint” is the British equivalent for peep) (C. minuta, C. ruficollis, C. temminckii, C. subminuta). These seven species range from 5 to 6½ inches (15-17 cm) in length, and weigh from 2/3 to 1½ ounces (17-33 g). -
Sunset Sanderlings
SANDERLING MOLT Digital photography leads to novel insights about the presupplemental molt of the Sanderling NOTE: All live Sanderling photos in this article are PETER PYLE from the spring of 2019 at Ocean Beach or Fort Fun- San Francisco, California ston Beach, San Francisco, California. Except for Fig. [email protected] 8, all photographs and figures by © Peter Pyle. This is publication #628 of The Institute for Bird Populations. 30 BIRDING | AUGUST 2019 fter moving to San Francisco’s Sunset District in Jan. 2019, I had to find some new local patches, Ocean Beach quickly becoming one of them, and I would head down the hill two or three mornings per week Aon my way to work. Although my original goal was to analyze formative/first-alternate1 feathers in gulls, the Sanderlings soon captured my attention. They were a nutty bunch, hun- dreds of them, running up and down and across and over, chasing each other at top speed, squabbling over mole crabs, and ganging up on small dogs. When big dogs went after the Sanderlings, the Common Ravens came to their rescue, at- tacking the canines and driving them off. Sometimes, for no apparent reason, the Sanderlings freaked out and flew out to sea, a behavior known as “silent dread” in gulls. At other times, dozens or hundreds tended “gardens,” probing patches of heavily bill-pocked sand, indistinguish- able from the rest of the beach, but undoubtedly harboring some favored morsels of food. Then there was the morning, in the middle of January, when I noticed a plucky Sander- ling sitting atop the crosswalk sign at Pacheco Street and the Great Highway, about 100 meters from the ocean, sing- ing! It struck me that the Ocean Beach Sanderlings have perhaps acquired the human behavioral eccentricity of These Sanderlings are “tending a garden” at Ocean Beach, San Francisco, on May 6, 2019. -
Conservation Status of New Zealand Birds, 2008
Notornis, 2008, Vol. 55: 117-135 117 0029-4470 © The Ornithological Society of New Zealand, Inc. Conservation status of New Zealand birds, 2008 Colin M. Miskelly* Wellington Conservancy, Department of Conservation, P.O. Box 5086, Wellington 6145, New Zealand [email protected] JOHN E. DOWDING DM Consultants, P.O. Box 36274, Merivale, Christchurch 8146, New Zealand GRAEME P. ELLIOTT Research & Development Group, Department of Conservation, Private Bag 5, Nelson 7042, New Zealand RODNEY A. HITCHMOUGH RALPH G. POWLESLAND HUGH A. ROBERTSON Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand PAUL M. SAGAR National Institute of Water & Atmospheric Research, P.O. Box 8602, Christchurch 8440, New Zealand R. PAUL SCOFIELD Canterbury Museum, Rolleston Ave, Christchurch 8001, New Zealand GRAEME A. TAYLOR Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand Abstract An appraisal of the conservation status of the post-1800 New Zealand avifauna is presented. The list comprises 428 taxa in the following categories: ‘Extinct’ 20, ‘Threatened’ 77 (comprising 24 ‘Nationally Critical’, 15 ‘Nationally Endangered’, 38 ‘Nationally Vulnerable’), ‘At Risk’ 93 (comprising 18 ‘Declining’, 10 ‘Recovering’, 17 ‘Relict’, 48 ‘Naturally Uncommon’), ‘Not Threatened’ (native and resident) 36, ‘Coloniser’ 8, ‘Migrant’ 27, ‘Vagrant’ 130, and ‘Introduced and Naturalised’ 36. One species was assessed as ‘Data Deficient’. The list uses the New Zealand Threat Classification System, which provides greater resolution of naturally uncommon taxa typical of insular environments than the IUCN threat ranking system. New Zealand taxa are here ranked at subspecies level, and in some cases population level, when populations are judged to be potentially taxonomically distinct on the basis of genetic data or morphological observations. -
Woodcock Research Group &Lpar;IWRB&Rpar;
Woodcock Research Group (IWRB) MONICA SHORTEN East Gate, Old Castle Road, Salisbury, WiltshireSP1 3SF, UK Citation: Shorten, M. 1975. Woodcock Research Group (IWRB). Wader Study Group Bull. 15: 12. The exasperatingWoodcock Scolopax rusticola is a 'fringe measurementsof bill length and central tail feathers, ex- species'amongst waders and waterfowl and woodland game, pressedas a ratio, allow adultmales and females to be con- and tendsto be neglectedin any group study.Woodcock fused: the best that can be done without dissection is to use enthusiastsare perhapsas odd and solitaryas the bird they the formula of Stronach, Harrington & Wilkins which have chosen,and the new Woodcock ResearchGroup of reducesthe probabilityof error to 28%: IWRB is strivingto flush someand induce flocking behav- iour. -0.2952 x bill length + 0.1566 x centraltail featherlength: [...] It seemsthat the occasionalWoodcock does get ringedby if greaterthan -8.3640 = male (72% correct),and theWSG - a total of five wasrecorded for 1974- thankyou, if less than -8.3640 = female (75% correct). TRG andHumber! The captureand ringing of this bird dur- ing its breedingseason really separatesthe men from the Birds in their first twelve monthsafter hatchingmust be boys,yet thereis a greatneed for 600-700, mainly pulli or excluded,and this can be done by examiningthe tips and juveniles,to be ringedin the BritishIsles each year. It has proximaledges of theouter primaries (ragged outline on first not beenmet since 1935 (763 pulli) and the averageyearly years;smooth on olderbirds, at leastuntil April) andthe ter- total, including FGs on migration, has been about 30 in minal lighter bar on primary coverts(broader and browner recentyears with pulli averagingabout 8.