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Rare Birds of California Now Available! Price $54.00 for WFO Members, $59.99 for Nonmembers
Volume 40, Number 3, 2009 The 33rd Report of the California Bird Records Committee: 2007 Records Daniel S. Singer and Scott B. Terrill .........................158 Distribution, Abundance, and Survival of Nesting American Dippers Near Juneau, Alaska Mary F. Willson, Grey W. Pendleton, and Katherine M. Hocker ........................................................191 Changes in the Winter Distribution of the Rough-legged Hawk in North America Edward R. Pandolfino and Kimberly Suedkamp Wells .....................................................210 Nesting Success of California Least Terns at the Guerrero Negro Saltworks, Baja California Sur, Mexico, 2005 Antonio Gutiérrez-Aguilar, Roberto Carmona, and Andrea Cuellar ..................................... 225 NOTES Sandwich Terns on Isla Rasa, Gulf of California, Mexico Enriqueta Velarde and Marisol Tordesillas ...............................230 Curve-billed Thrasher Reproductive Success after a Wet Winter in the Sonoran Desert of Arizona Carroll D. Littlefield ............234 First North American Records of the Rufous-tailed Robin (Luscinia sibilans) Lucas H. DeCicco, Steven C. Heinl, and David W. Sonneborn ........................................................237 Book Reviews Rich Hoyer and Alan Contreras ...........................242 Featured Photo: Juvenal Plumage of the Aztec Thrush Kurt A. Radamaker .................................................................247 Front cover photo by © Bob Lewis of Berkeley, California: Dusky Warbler (Phylloscopus fuscatus), Richmond, Contra Costa County, California, 9 October 2008, discovered by Emilie Strauss. Known in North America including Alaska from over 30 records, the Dusky is the Old World Warbler most frequent in western North America south of Alaska, with 13 records from California and 2 from Baja California. Back cover “Featured Photos” by © Kurt A. Radamaker of Fountain Hills, Arizona: Aztec Thrush (Ridgwayia pinicola), re- cently fledged juvenile, Mesa del Campanero, about 20 km west of Yecora, Sonora, Mexico, 1 September 2007. -
Merritt Island National Wildlife Refuge BIRD LIST
Merrritt Island National Wildlife Refuge U.S. Fish & Wildlife Service P.O. Box 2683 Titusville, FL 32781 http://www.fws.gov/refuge/Merritt_Island 321/861 0669 Visitor Center Merritt Island U.S. Fish & Wildlife Service 1 800/344 WILD National Wildlife Refuge March 2019 Bird List photo: James Lyon Merritt Island National Wildlife Refuge, located just Seasonal Occurrences east of Titusville, shares a common boundary with the SP - Spring - March, April, May John F. Kennedy Space Center. Its coastal location, SU - Summer - June, July, August tropic-like climate, and wide variety of habitat types FA - Fall - September, October, November contribute to Merritt Island’s diverse bird population. WN - Winter - December, January, February The Florida Ornithological Society Records Committee lists 521 species of birds statewide. To date, 359 You may see some species outside the seasons indicated species have been identified on the refuge. on this checklist. This phenomenon is quite common for many birds. However, the checklist is designed to Of special interest are breeding populations of Bald indicate the general trend of migration and seasonal Eagles, Brown Pelicans, Roseate Spoonbills, Reddish abundance for each species and, therefore, does not Egrets, and Mottled Ducks. Spectacular migrations account for unusual occurrences. of passerine birds, especially warblers, occur during spring and fall. In winter tens of thousands of Abundance Designation waterfowl may be seen. Eight species of herons and C – Common - These birds are present in large egrets are commonly observed year-round. numbers, are widespread, and should be seen if you look in the correct habitat. Tips on Birding A good field guide and binoculars provide the basic U – Uncommon - These birds are present, but because tools useful in the observation and identification of of their low numbers, behavior, habitat, or distribution, birds. -
Ivory-Billed Woodpecker Fact Sheet
Ivory-Billed Woodpecker Fact Sheet Common Name: Ivory-Billed Woodpecker Scientific Name: Campephilus principalis Wild Status: Critically Endangered - heavily believed to be extinct Habitat: Pine Forests, thick hardwood swamp areas Country: Southeastern United States, and a subspecies native to Cuba Shelter: Trees Life Span: Unknown - some speculate up to 20 years or more Size: Weighs about 1 pound on average, total length roughly 20 inches, with a typical 30 inch wingspan Details The Ivory-Billed Woodpecker is a very rare bird, native to the Southeast of the United States. They are one of the largest woodpeckers in the world, and noticeable by their distinct black and white pattern and red plumage near their head. Primarily due to habitat loss, as well as hunting to a lesser extent, the Ivory-Billed Woodpecker is classified as critically endangered. However, many associations and biologists believe the species to be functionally extinct, as true sightings and evidence of living specimens has not been published in over 10 years. The Ivory-Billed Woodpecker is believed to mate for life like many birds, and both parents would work together to create a nest for the young. Much of the woodpecker's diet consists of larvae and insects, as well as seeds and fruit. Cool Facts • They are sexually dimorphic - only the males have the red plumage on their head. • Four distinct vocal calls were noted in literature, and two of these calls were recorded in the 1930s. • While many unconfirmed reports still come in, this species was assessed as extinct in 1994. However, this was later altered to critically endangered on the belief that the species might have relocated from their native habitat. -
Appendix C. Texas Birds Including Those Found in Three Urban Centers and in Other States
Appendix C. Texas birds including those found in three urban centers and in other states. (Courtesy of Cassandra LaFleur) Texas Birds Scientific Name Austin Dallas Houston States Checklistb 1. Acadian Flycatcher (Empidonax virescens) H 38 2. Acorn Woodpecker (Melanerpes formicivorus) 14 3. Alder Flycatcher (Empidonax alnorum) 42 4. Allen's Hummingbird (Selasphorus sasin) 20 5. Altamira Oriole (Icterus gularis) 1 6. American Avocet (Recurvirostra americana) D 49 7. American Bittern (Botaurus lentiginosus) H 49 8. American Black Duck (Anas rubripes) 47 9. American Coot (Fulica americana) D H 50 10. American Crow (Corvus brachyrhynchos) Da H 49 11. American Dipper (Cinclus mexicanus) 16 12. American Flamingo (Phoenicopterus ruber) 8 13. American Golden-Plover (Pluvialis dominica) 48 14. American Goldfinch (Spinus tristis) A D H 49 15. American Kestrel (Falco sparverius) D H 49 16. American Oystercatcher (Haematopus palliatus) 21 17. American Pipit (Anthus rubescens) 50 18. American Redstart (Setophaga ruticilla) Da 49 19. American Robin (Turdus migratorius) A Da H 49 20. American Tree Sparrow (Spizella arborea) 49 (Pelecanus 21. American White Pelican D 49 erythrorhynchos) 22. American Wigeon (Anas americana) D 50 23. American Woodcock (Scolopax minor) H 42 24. Anhinga (Anhinga anhinga) D 37 25. Anna's Hummingbird (Calypte anna) 30 26. Aplomado Falcon (Falco femoralis) 3 27. Arctic Tern (Sterna paradisaea) 44 28. Ash-throated Flycatcher (Myiarchus cinerascens) 39 29. Audubon's Oriole (Icterus graduacauda) 2 30. Audubon's Shearwater (Puffinus lherminieri) 17 31. Aztec Thrush (Ridgwayia pinicola) 2 32. Bachman's Sparrow (Peucaea aestivalis) 24 33. Baird's Sandpiper (Calidris bairdii) 50 34. Bald Eagle (Haliaeetus leucocephalus) D H 49 35. -
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 -
Houde2009chap64.Pdf
Cranes, rails, and allies (Gruiformes) Peter Houde of these features are subject to allometric scaling. Cranes Department of Biology, New Mexico State University, Box 30001 are exceptional migrators. While most rails are generally MSC 3AF, Las Cruces, NM 88003-8001, USA ([email protected]) more sedentary, they are nevertheless good dispersers. Many have secondarily evolved P ightlessness aJ er col- onizing remote oceanic islands. Other members of the Abstract Grues are nonmigratory. 7 ey include the A nfoots and The cranes, rails, and allies (Order Gruiformes) form a mor- sungrebe (Heliornithidae), with three species in as many phologically eclectic group of bird families typifi ed by poor genera that are distributed pantropically and disjunctly. species diversity and disjunct distributions. Molecular data Finfoots are foot-propelled swimmers of rivers and lakes. indicate that Gruiformes is not a natural group, but that it 7 eir toes, like those of coots, are lobate rather than pal- includes a evolutionary clade of six “core gruiform” fam- mate. Adzebills (Aptornithidae) include two recently ilies (Suborder Grues) and a separate pair of closely related extinct species of P ightless, turkey-sized, rail-like birds families (Suborder Eurypygae). The basal split of Grues into from New Zealand. Other extant Grues resemble small rail-like and crane-like lineages (Ralloidea and Gruoidea, cranes or are morphologically intermediate between respectively) occurred sometime near the Mesozoic– cranes and rails, and are exclusively neotropical. 7 ey Cenozoic boundary (66 million years ago, Ma), possibly on include three species in one genus of forest-dwelling the southern continents. Interfamilial diversifi cation within trumpeters (Psophiidae) and the monotypic Limpkin each of the ralloids, gruoids, and Eurypygae occurred within (Aramidae) of both forested and open wetlands. -
A Classification of the Rallidae
A CLASSIFICATION OF THE RALLIDAE STARRY L. OLSON HE family Rallidae, containing over 150 living or recently extinct species T and having one of the widest distributions of any family of terrestrial vertebrates, has, in proportion to its size and interest, received less study than perhaps any other major group of birds. The only two attempts at a classifi- cation of all of the recent rallid genera are those of Sharpe (1894) and Peters (1934). Although each of these lists has some merit, neither is satisfactory in reflecting relationships between the genera and both often separate closely related groups. In the past, no attempt has been made to identify the more primitive members of the Rallidae or to illuminate evolutionary trends in the family. Lists almost invariably begin with the genus Rdus which is actually one of the most specialized genera of the family and does not represent an ancestral or primitive stock. One of the difficulties of rallid taxonomy arises from the relative homo- geneity of the family, rails for the most part being rather generalized birds with few groups having morphological modifications that clearly define them. As a consequence, particularly well-marked genera have been elevated to subfamily rank on the basis of characters that in more diverse families would not be considered as significant. Another weakness of former classifications of the family arose from what Mayr (194933) referred to as the “instability of the morphology of rails.” This “instability of morphology,” while seeming to belie what I have just said about homogeneity, refers only to the characteristics associated with flightlessness-a condition that appears with great regularity in island rails and which has evolved many times. -
Periodic and Transient Motions of Large Woodpeckers Michael D
www.nature.com/scientificreports Correction: Publisher Correction OPEN Periodic and transient motions of large woodpeckers Michael D. Collins Two types of periodic and transient motions of large woodpeckers are considered. A drumming Received: 3 July 2017 woodpecker may be modeled as a harmonic oscillator with a periodic forcing function. The transient Accepted: 12 September 2017 behavior that occurs after the forcing is turned of suggests that the double knocks of Campephilus Published: xx xx xxxx woodpeckers may be modeled in terms of a harmonic oscillator with an impulsive forcing, and this hypothesis is consistent with audio and video recordings. Wingbeats are another type of periodic and transient motion of large woodpeckers. A model for the fap rate in cruising fight is applied to the Pileated Woodpecker (Dryocopus pileatus) and the Ivory-billed Woodpecker (Campephilus principalis). During a brief transient just after taking of, the wing motion and fap rate of a large woodpecker may not be the same as in cruising fight. These concepts are relevant to videos that contain evidence for the persistence of the Ivory-billed Woodpecker. Drumming and wingbeats are two types of periodic motion of large woodpeckers. Tis paper discusses these behaviors and related transient motions that occur in evidence for the persistence of the Ivory-billed Woodpecker (Campephilus principalis)1–3. Most woodpeckers signal by drumming, which consists of a rapid series of blows with the bill. Audio S1 contains four drumming events by nearby and distant Pileated Woodpeckers (Dryocopus pileatus). Some members of the Campephilus genus do not engage in this type of drumming but instead signal with double knocks. -
A Description of Mixed-Species Insectivorous Bird Flocks in Western Mexico’
The Condor 89~282-292 0 The Cooper Omithologml Society 1987 A DESCRIPTION OF MIXED-SPECIES INSECTIVOROUS BIRD FLOCKS IN WESTERN MEXICO’ RICHARD L. HUTTO Department of Zoology, Universityof Montana, Missoula, MT 59812 Abstract. Insectivorousbird flockswere observed in all typesof forestedhabitats during the nonbreedingseason in westernMexico. The speciescomposition of flockschanged markedlyand predictablyamong five categoriesof habitat type. The averagenumber of speciesper flockin lowlandhabitats was 4.7, while a mean of 18.6 speciesparticipated in highlandflocks, ranking the latter amongthe most species-richflocks in the world. The meanproportion of the localinsectivorous species that participatedin mixed-speciesflocks wassignificantly greater in the highlands(6 1.3%)than in the lowlands(24.6%). About half of the flock participantsin both undisturbedlowland and highlandhabitats were north temperatemigrants, ranking west Mexican flocks among the mostmigrant-rich in the world as well. In highlandflocks, the maximum numberof individualsper attendantspecies was generallytwo to three,but therewere often six to twelveindividuals belonging to eachof severalnuclear species. The lowlanddeciduous forest flocks seemed to lack nuclearspecies. Key words: Mixed-speciesflocks; insectivorousbirds; Mexico; migratory birds;pine-oak woodlands;tropical deciduous forests. INTRODUCTION mixed-speciesflocks in 26 sites(Appendix I) that Mixed-speciesinsectivorous bird flockshave been were distributed among various habitats described from temperate and tropical areas throughout western Mexico. The habitat types worldwide (Rand 1954), and are known to occur that I surveyed can be roughly classified (after in practically every habitat type (Powell 1985). Pesman 1962) as belonging to either lowland Although mixed-species flocks are quite com- (tropical deciduous and tropical evergreen) or mon in north temperate regions during the non- highland (oak, pine-oak, and boreal) forests. -
Merritt Island National Wildlife Refuge
Merritt Island National Wildlife Refuge Comprehensive Conservation Plan U.S. Department of the Interior Fish and Wildlife Service Southeast Region August 2008 COMPREHENSIVE CONSERVATION PLAN MERRITT ISLAND NATIONAL WILDLIFE REFUGE Brevard and Volusia Counties, Florida U.S. Department of the Interior Fish and Wildlife Service Southeast Region Atlanta, Georgia August 2008 TABLE OF CONTENTS COMPREHENSIVE CONSERVATION PLAN EXECUTIVE SUMMARY ....................................................................................................................... 1 I. BACKGROUND ................................................................................................................................. 3 Introduction ................................................................................................................................... 3 Purpose and Need for the Plan .................................................................................................... 3 U.S. Fish And Wildlife Service ...................................................................................................... 4 National Wildlife Refuge System .................................................................................................. 4 Legal Policy Context ..................................................................................................................... 5 National Conservation Plans and Initiatives .................................................................................6 Relationship to State Partners ..................................................................................................... -
Programs and Field Trips
CONTENTS Welcome from Kathy Martin, NAOC-V Conference Chair ………………………….………………..…...…..………………..….…… 2 Conference Organizers & Committees …………………………………………………………………..…...…………..……………….. 3 - 6 NAOC-V General Information ……………………………………………………………………………………………….…..………….. 6 - 11 Registration & Information .. Council & Business Meetings ……………………………………….……………………..……….………………………………………………………………………………………………………………….…………………………………..…..……...….. 11 6 Workshops ……………………….………….……...………………………………………………………………………………..………..………... 12 Symposia ………………………………….……...……………………………………………………………………………………………………..... 13 Abstracts – Online login information …………………………..……...………….………………………………………….……..……... 13 Presentation Guidelines for Oral and Poster Presentations …...………...………………………………………...……….…... 14 Instructions for Session Chairs .. 15 Additional Social & Special Events…………… ……………………………..………………….………...………………………...…………………………………………………..…………………………………………………….……….……... 15 Student Travel Awards …………………………………………..………...……………….………………………………..…...………... 18 - 20 Postdoctoral Travel Awardees …………………………………..………...………………………………..……………………….………... 20 Student Presentation Award Information ……………………...………...……………………………………..……………………..... 20 Function Schedule …………………………………………………………………………………………..……………………..…………. 22 – 26 Sunday, 12 August Tuesday, 14 August .. .. .. 22 Wednesday, 15 August– ………………………………...…… ………………………………………… ……………..... Thursday, 16 August ……………………………………….…………..………………………………………………………………… …... 23 Friday, 17 August ………………………………………….…………...………………………………………………………………………..... 24 Saturday, -
Anatomical Evidence for Phylogenetic Relationships Among Woodpeckers
ANATOMICAL EVIDENCE FOR PHYLOGENETIC RELATIONSHIPS AMONG WOODPECKERS WILLIAM R. GOODGE ALT•tOUCr•the functionalanatomy of woodpeckershas long been a subjectof interest,their internal anatomyhas not been usedextensively for determiningprobable phylogeneticrelationships within the family. In part this is probablydue to the reluctanceto use highly adaptivefea- tures in phylogeneticstudies becauseof the likelihood of convergent evolution. Bock (1967) and othershave pointedout that adaptivehess in itself doesnot rule out taxonomicusefulness, and that the highly adaptivefeatures will probablybe the oneshaving conspicuous anatomical modifications,and Bock emphasizesthe need for detailedstudies of func- tion beforeusing featuresin studiesof phylogeny.Although valuable, functionalconclusions are often basedon inferencesnot backed up by experimentaldata. As any similaritybetween species is possiblydue to functionalconvergence, I believewhat is neededmost is detailedstudy of a numberof featuresin order to distinguishbetween similarities re- sultingfrom convergenceand thosebased on phylogenticrelationship. Simplestructures are not necessarilymore primitive and morphological trendsare reversible,as Mayr (1955) has pointedout. Individual varia- tion may occur and various investigatorsmay interpret structuresdif- ferently. Despite these limitations,speculation concerning phylogeny will continuein the future,and I believethat it shouldbe basedon more, rather than fewer anatomical studies. MATERIALS AND METItODS Alcoholic specimensrepresenting 33 genera