Bird Species List for Glacier Creek Preserve This Bird Species List Includes Observations and Documented Surveys Ranging from the Late 1990'S to Present
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First Occurrence of Black-Chinned Hummingbird in Alabama
RARE OCCURRENCE First occurrence of Black-chinned Bummingbirdin Alabama With notes on identification Greg D. Jackson Photo/GregD. Jackson. 178 AmericanBirds, Summer 1988 observeddunng the courseof the hum- taft-pumpingof the Black-ch•nned•s b•rd (ArchtlochusalexandrO has m•ngb•rd'sstay. The b•rd wasthe same very noticeable whfie feeding, and •s beenHEBLACK-CHINNEDreported casually from HUMMING- Florida sizeas a Ruby-throated Hummingbird. generallymore frequentand persistent (Hoffman 1983)and is an annualvisitor The bill waslonger than that of a Ruby- than that shownby the Ruby-throated to southeasternLouisiana (N. L. New- throated. The wingswere pointed, but Hummingbird (N. L. Newfield pers field pers. comm.), but until January the outermostprimary had an obtuse comm.). Immature males of either spe- 1984 had never been recorded in Ala- subterminal angulation and a broad, ciescan showsome characteristic gorget bama. Besides the breeding Ruby- blunt tip. The tail, which was pumped colorby early fall (Scott 1983). throated Hummingbird (Archilochus constantlywhile feeding,had a mod- colubris),the only other member of this eratelydeep central notch when folded, family recordedin Alabamais the Ru- and was rather square with a shallow fousHummingbird (Selasphorus rufus), notch when spread.The crown and face which is a rare visitorin migrationand weredark gray-green.There wasa short w•nter (Imhof 1976). The first docu- white stripe posterior to the eye. The mented occurrence of the Black- dorsal surface of the tail showed black ACKNOWLEDGMENTS ch•nned Hummingbird in the state is outer rectrices and dark green inner from the Spring Hill district of Mobile rectrices.The remainder of the upper- The author is grateful to Nancy L. -
Complete Species Table in Species Number Order
Page 1 of 19 Complete Species Table in Species Number order Go to species 100 .0, 200 .0, 300 .0, 400 .0, 500 .0, 600 .0, 700 .0, 800 .0, 900 .0 SPECIES COMMON NAME ALPHA CODE BAND SIZE 001 .0 Western Grebe WEGR 7A 7B 001 .1 Clark's Grebe CLGR 7A 7B 002 .0 Red-necked Grebe RNGR 7A 003 .0 Horned Grebe HOGR 6 5 004 .0 Eared Grebe EAGR 5 005 .0 Least Grebe LEGR 4 006 .0 Pied-billed Grebe PBGR 5 6 007 .0 Common Loon COLO 8 008 .0 Yellow-billed Loon YBLO 9 009 .0 Arctic Loon ARLO 7B 010 .0 Pacific Loon PALO 7B 011 .0 Red-throated Loon RTLO 7B 012 .0 Tufted Puffin TUPU 6 5 013 .0 Atlantic Puffin ATPU 5 014 .0 Horned Puffin HOPU 5 015 .0 Rhinoceros Auklet RHAU 5 6 016 .0 Cassin's Auklet CAAU 3B-3A 017 .0 Parakeet Auklet PAAU 4 018 .0 Crested Auklet CRAU 4 019 .0 Whiskered Auklet WHAU 3 020 .0 Least Auklet LEAU 2 3 021 .0 Ancient Murrelet ANMU 3B 3 023 .0 Marbled Murrelet MAMU 3B 3 023 .1 Long-billed Murrelet LBMU 3B 3 024 .0 Kittlitz's Murrelet KIMU 3B 025 .0 Xantus's Murrelet XAMU 2 026 .0 Craveri's Murrelet CRMU 2 027 .0 Black Guillemot BLGU 4 029 .0 Pigeon Guillemot PIGU 4A 030 .0 Common Murre COMU 6M 031 .0 Thick-billed Murre TBMU 6M 5R 032 .0 Razorbill RAZO 5R 034 .0 Dovekie DOVE 3 035 .0 Great. -
Breeding of the Leach's Storm-Petrel Oceanodroma Leucorhoa at Santa Catalina Island, California
Carter et al.: Leach’s Storm-Petrel at Santa Catalina Island 83 BREEDING OF THE LEACH’S STORM-PETREL OCEANODROMA LEUCORHOA AT SANTA CATALINA ISLAND, CALIFORNIA HARRY R. CARTER1,3,4, TYLER M. DVORAK2 & DARRELL L. WHITWORTH1,3 1California Institute of Environmental Studies, 3408 Whaler Avenue, Davis, CA 95616, USA 2Catalina Island Conservancy, 125 Clarissa Avenue, Avalon, CA 90704, USA 3Humboldt State University, Department of Wildlife, 1 Harpst Street, Arcata, CA 95521, USA 4Current address: Carter Biological Consulting, 1015 Hampshire Road, Victoria, BC V8S 4S8, Canada ([email protected]) Received 4 November 2015, accepted 5 January 2016 Among the California Channel Islands (CCI) off southern California, Guadalupe Island, off central-west Baja California (Ainley 1980, the Ashy Storm-Petrel Oceanodroma homochroa (ASSP) is the Power & Ainley 1986, Ainley 2005, Pyle 2008, Howell et al. most numerous and widespread breeding storm-petrel; it is known 2009). Alternatively, these egg specimens may have been from to breed at San Miguel, Santa Cruz, Anacapa, Santa Barbara, and dark-rumped LESP, which are known to breed at the Coronado San Clemente islands (Hunt et al. 1979, 1980; Sowls et al. 1980; and San Benito islands, Baja California (Ainley 1980, Power & Carter et al. 1992, 2008; Harvey et al. 2016; Fig. 1B; Appendix 1, Ainley 1986). available on the website). Low numbers of Black Storm-Petrels O. melania (BLSP) also breed at Santa Barbara Island (Pitman Within this context, we asked the following questions: (1) Were the & Speich 1976; Hunt et al. 1979, 1980; Carter et al. 1992; 1903 egg records the first breeding records of LESP at Catalina and Appendix 1). -
Possible Relationship Between Vocal Communication System and Fat Reserve in Wintering Birds: a Test of the Optimal Body Mass Theory
POSSIBLE RELATIONSHIP BETWEEN VOCAL COMMUNICATION SYSTEM AND FAT RESERVE IN WINTERING BIRDS: A TEST OF THE OPTIMAL BODY MASS THEORY A Thesis by Gamage Dilini Nuwanthika Perera Bachelor of Science, University of Peradeniya, 2014 Submitted to the Department of Biological Sciences and the faculty of the Graduate School of Wichita State University in partial fulfillment of the requirements for the degree of Master of Science December 2017 ©Copyright 2017 by Gamage Dilini Nuwanthika Perera All Rights Reserved POSSIBLE RELATIONSHIP BETWEEN VOCAL COMMUNICATION SYSTEM AND FAT RESERVE IN WINTERING BIRDS: A TEST OF THE OPTIMAL BODY MASS THEORY The following faculty members have examined the final copy of this thesis for form and content, and recommend that it be accepted in partial fulfillment of the requirement for the degree of Master of Science with a major in Biological Sciences. F. Leland Russell, Committee Chair Mark A. Schneegurt, Committee Member Kandatege Wimalasena, Committee Member iii DEDICATION To my parents, family and friends who always encouraged and supported me, and made me the person I am today. iv ACKNOWLEDGEMENTS I would like to thank my advisers, Christopher M. Rogers and F. Leland Russell for their many months of thoughtful, patient guidance and support along the journey of my graduate career. I would also like to thank Wichita State University, for the use of their facilities and resources. WSU has provided a great opportunity for me to proceed along the journey that is graduate school. I thank especially F. Leland Russell for taking responsibility for me after Christopher Rogers was on medical leave. Finally thanks to my family, friends and colleagues for their support and encouragement throughout my career. -
A Multi-Gene Phylogeny of Aquiline Eagles (Aves: Accipitriformes) Reveals Extensive Paraphyly at the Genus Level
Available online at www.sciencedirect.com MOLECULAR SCIENCE•NCE /W\/Q^DIRI DIRECT® PHYLOGENETICS AND EVOLUTION ELSEVIER Molecular Phylogenetics and Evolution 35 (2005) 147-164 www.elsevier.com/locate/ympev A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level Andreas J. Helbig'^*, Annett Kocum'^, Ingrid Seibold^, Michael J. Braun^ '^ Institute of Zoology, University of Greifswald, Vogelwarte Hiddensee, D-18565 Kloster, Germany Department of Zoology, National Museum of Natural History, Smithsonian Institution, 4210 Silver Hill Rd., Suitland, MD 20746, USA Received 19 March 2004; revised 21 September 2004 Available online 24 December 2004 Abstract The phylogeny of the tribe Aquilini (eagles with fully feathered tarsi) was investigated using 4.2 kb of DNA sequence of one mito- chondrial (cyt b) and three nuclear loci (RAG-1 coding region, LDH intron 3, and adenylate-kinase intron 5). Phylogenetic signal was highly congruent and complementary between mtDNA and nuclear genes. In addition to single-nucleotide variation, shared deletions in nuclear introns supported one basal and two peripheral clades within the Aquilini. Monophyly of the Aquilini relative to other birds of prey was confirmed. However, all polytypic genera within the tribe, Spizaetus, Aquila, Hieraaetus, turned out to be non-monophyletic. Old World Spizaetus and Stephanoaetus together appear to be the sister group of the rest of the Aquilini. Spiza- stur melanoleucus and Oroaetus isidori axe nested among the New World Spizaetus species and should be merged with that genus. The Old World 'Spizaetus' species should be assigned to the genus Nisaetus (Hodgson, 1836). The sister species of the two spotted eagles (Aquila clanga and Aquila pomarina) is the African Long-crested Eagle (Lophaetus occipitalis). -
Birds of the East Texas Baptist University Campus with Birds Observed Off-Campus During BIOL3400 Field Course
Birds of the East Texas Baptist University Campus with birds observed off-campus during BIOL3400 Field course Photo Credit: Talton Cooper Species Descriptions and Photos by students of BIOL3400 Edited by Troy A. Ladine Photo Credit: Kenneth Anding Links to Tables, Figures, and Species accounts for birds observed during May-term course or winter bird counts. Figure 1. Location of Environmental Studies Area Table. 1. Number of species and number of days observing birds during the field course from 2005 to 2016 and annual statistics. Table 2. Compilation of species observed during May 2005 - 2016 on campus and off-campus. Table 3. Number of days, by year, species have been observed on the campus of ETBU. Table 4. Number of days, by year, species have been observed during the off-campus trips. Table 5. Number of days, by year, species have been observed during a winter count of birds on the Environmental Studies Area of ETBU. Table 6. Species observed from 1 September to 1 October 2009 on the Environmental Studies Area of ETBU. Alphabetical Listing of Birds with authors of accounts and photographers . A Acadian Flycatcher B Anhinga B Belted Kingfisher Alder Flycatcher Bald Eagle Travis W. Sammons American Bittern Shane Kelehan Bewick's Wren Lynlea Hansen Rusty Collier Black Phoebe American Coot Leslie Fletcher Black-throated Blue Warbler Jordan Bartlett Jovana Nieto Jacob Stone American Crow Baltimore Oriole Black Vulture Zane Gruznina Pete Fitzsimmons Jeremy Alexander Darius Roberts George Plumlee Blair Brown Rachel Hastie Janae Wineland Brent Lewis American Goldfinch Barn Swallow Keely Schlabs Kathleen Santanello Katy Gifford Black-and-white Warbler Matthew Armendarez Jordan Brewer Sheridan A. -
Why So Many Kinds of Passerine Birds?
Letters • Why so many kinds of passerine birds? Raikow and Bledsoe (2000), in em- Slud 1976). It is unreasonable to assume the list of possible reasons for passerine bracing the null model of Slowinski that there is no underlying biological rea- success, but I would place more empha- and Guyer (1989a, 1989b), may perhaps son for this pattern and for the major sis on it than he did. be said literally to have added nothing turnover in avifaunas in the Northern It is difficult to discuss the nest-bufld- to the Kst of suggestions for why there are Hemisphere in favor of passerines after ing capabilities of passerines without re- so many species of passerine birds. When the Oligocène. sorting to anthropomorphisms such as Raikow (1986) addressed this problem Reproductive adaptations presumably "clever" or "ingenious." Is it not mar- previously and could find no key mor- made the holometabolous insects velous, however, that a highly special- phological adaptations to explain the di- (Coleóptera, Díptera, Hymenoptera, ized aerial feeder such as a cliff swallow versity of Passeriformes, the so-called Lepidoptera, and so on) the dominant (Hirundo pyrrhonota), with tiny, weak songbirds or perching birds, he despaired clade of organisms on earth. Likewise, it bill and feet, can fashion a complex nest and suggested that the problem may be appears that reproductive adaptations, out of gobs of mud fastened to a flat, only "an accident of classificatory his- not morphology, are responsible for the vertical surface? What adjective suffices tory," which brought on a storm of protest dominance of passerine birds over other to describe the nest of tailorbirds {Systematic Zoology 37: 68-76; 41: 242- orders of birds. -
Bald Eagle Haliaeetus Leucocephalus
Wyoming Species Account Bald Eagle Haliaeetus leucocephalus REGULATORY STATUS USFWS: Delisted; Migratory Bird USFS R2: Sensitive USFS R4: Sensitive Wyoming BLM: Sensitive State of Wyoming: Protected Bird CONSERVATION RANKS USFWS: Bird of Conservation Concern WGFD: NSS3 (Bb), Tier II WYNDD: G5, S4B/S5N Wyoming Contribution: LOW IUCN: Least Concern PIF Continental Concern Score: 9 STATUS AND RANK COMMENTS Bald Eagle (Haliaeetus leucocephalus) is provided international protection under the Federal Migratory Bird Treaty Act of 1918, as amended 1. In 1940, Bald Eagle was provided protection under the Bald and Golden Eagle Protection Act 2. In 1966, the southern subspecies was listed as federally endangered under the Endangered Species Preservation Act; the entire population in the contiguous United States was listed as endangered in 1978 under the 1973 Endangered Species Act (ESA). A significant increase in numbers of nesting pairs, productivity, and distribution allowed Bald Eagle to be reclassified from Endangered to Threatened in 1995 under the ESA 3. Bald Eagle was delisted in 2007, and numbers are considered to be stable to increasing across its range 4. The species has been assigned different state conservation ranks by the Wyoming Natural Diversity Database for the breeding season and nonbreeding season because the abundance of the species is different between seasons. NATURAL HISTORY Taxonomy: Bald Eagle is a member of the family Accipitridae, which includes kites, eagles, harriers, and hawks 5. There are two subspecies of Bald Eagle; H. l. alascanus is found north of 40 degrees latitude across North America, including Wyoming, while H. l. leucocephalus is found south of 40 degrees latitude in the Gulf coast states 6. -
Wood Duck (Aix Sponsa), EC 1606 (Oregon State University Extension
EC 1606 • April 2007 $1.00 Wood Duck Photo: Dave Menke, U.S. Fish and Wildlife Service Aix sponsa by Z. Turnbull and S. Sells he wood duck is so beautiful that its populations have increased, and today scientifi c name, Aix sponsa, means populations are at healthy levels. T “water bird in bridal dress.” Being Wood ducks are very popular for hunt- so beautiful (and tasty!), by the 1880s, ing. In fact, there are more wood ducks the once-abundant wood duck was disap- harvested each year in the United States pearing quickly due to hunting and habitat than any other game bird except mallards. loss. But not just hunters appreciate wood In the 1910s, wildlife managers acted ducks. Bird watchers and other people quickly to help save wood ducks. Laws who spend time outdoors love their were passed to protect migratory birds, beauty. hunting was controlled, and habitat was Common predators of wood ducks are protected. Wood duck nest boxes were raccoons, gray and red foxes, great horned created in the 1930s. Slowly, wood duck owls, some snakes, and minks. In a group of 10 newly hatched wood ducks, usu- ally only one or two survive past their fi rst 2 weeks. Predation is a main cause of such low survival rates. Dump nests occur when one or more females follow another to her nest and add their own eggs to the fi rst female’s eggs. When this occurs, there may be 50 or more eggs. They usually are abandoned, leading to a decline in successful hatch- ings in the area. -
Diet of Three Sympatric Owls in Steppe Habitats of Eastern Kazakhstan
256 SHORT COMMUNICATIONS VOL. 37, NO. 3 Comfin en Espafia y Portugal (I Censo Coordinado). (Oypaetusbarbaras) en Catalufia (NE Espafia) e imph- Afio 2000. Monograf/a nø 8. SEO/BirdLife, Madrid, caciones sobre su conservacitn. Do•ana Acta Vertebr Spain. 24:235-243. DONAZAR,J.A. 1993. Los buitres ib•ricos. Biologla y con- PAm½ER,P.G., T.A. WAITE, AND M.D. DECKER. 1995. Kin- servacitn. J.M. Reyero, Madrid, Spain. ship and associationin communally roosting black --, O. CEBALLOS,AND J.L. TELLA. 1996. Communal vultures. Anita. Behar. 49:395-401. roostsof EgyptianVultures (Neophronpercnopterus): dy- RABENOLD, P.P. 1983. The communal roost in Black and namics and implicationsfor the speciesconservation. Turkey Vultures:an Information Center?Pages 303- Pages 189-201 in J. Muntaner and J. Mayol [EDS.], 321 in S.R. Wilbur and J.A. Jackson [EDS.], Vulture Biologia y Conservaci0n de las Rapaces Mediterr•- biology and management. Univ. of California Press, neas. Monografias No. 4 de la SEO, Madrid, Spain. Berkeley, CA U.S.A. ß 1987. Recruitment to food in black vultures: ev- --, c.J. PAI,ACIOS,L. GANOOSO,O. CEBALLOS,M.J. GONZ./•LEZ,AND F. HIRALDO. 2002. Conservation status idence for following from communal roosts.Anita. Be- hay. 35:1775-1785. and limiting factorsin the endangeredpopulation of TELLA,J.L. 1991. Dormideros de alimoches en el Valle EgyptianVulture (Neophronpercnopterus) in the Canary Islands. Bid. Conserv. 107:89-98. Medio del Ebro. ActasI CongresoInternacional sobre Aves Carrofieras: 69-74. AEDENAT-CODA, Madrid, MAROAL•D^,A. 1997. Aparici6n de un dormidero comu- Spain. nal de Alimoche (Neophronpercnopterus) en Catalufia ß 2001. -
Brown2009chap67.Pdf
Swifts, treeswifts, and hummingbirds (Apodiformes) Joseph W. Browna,* and David P. Mindella,b Hirundinidae, Order Passeriformes), and between the aDepartment of Ecology and Evolutionary Biology & University nectivorous hummingbirds and sunbirds (Family Nec- of Michigan Museum of Zoology, 1109 Geddes Road, University tariniidae, Order Passeriformes), the monophyletic sta- b of Michigan, Ann Arbor, MI 48109-1079, USA; Current address: tus of Apodiformes has been well supported in all of the California Academy of Sciences, 55 Concourse Drive Golden Gate major avian classiA cations since before Fürbringer (3). Park, San Francisco, CA 94118, USA *To whom correspondence should be addressed (josephwb@ A comprehensive historical review of taxonomic treat- umich.edu) ments is available (4). Recent morphological (5, 6), genetic (4, 7–12), and combined (13, 14) studies have supported the apodiform clade. Although a classiA cation based on Abstract large DNA–DNA hybridization distances (4) promoted hummingbirds and swiJ s to the rank of closely related Swifts, treeswifts, and hummingbirds constitute the Order orders (“Trochiliformes” and “Apodiformes,” respect- Apodiformes (~451 species) in the avian Superorder ively), the proposed revision does not inP uence evolu- Neoaves. The monophyletic status of this traditional avian tionary interpretations. order has been unequivocally established from genetic, One of the most robustly supported novel A ndings morphological, and combined analyses. The apodiform in recent systematic ornithology is a close relation- timetree shows that living apodiforms originated in the late ship between the nocturnal owlet-nightjars (Family Cretaceous, ~72 million years ago (Ma) with the divergence Aegothelidae, Order Caprimulgiformes) and the trad- of hummingbird and swift lineages, followed much later by itional Apodiformes. -
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.