Topazes and Hermits

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Trochilidae I: Topazes and Hermits Fiery Topaz, Topaza pyra Topazini Crimson Topaz, Topaza pella Florisuginae White-necked Jacobin, Florisuga mellivora Florisugini Black Jacobin, Florisuga fusca White-tipped Sicklebill, Eutoxeres aquila Eutoxerini Buﬀ-tailed Sicklebill, Eutoxeres condamini Saw-billed Hermit, Ramphodon naevius Bronzy Hermit, Glaucis aeneus Phaethornithinae Rufous-breasted Hermit, Glaucis hirsutus ?Hook-billed Hermit, Glaucis dohrnii Threnetes ruckeri Phaethornithini Band-tailed Barbthroat, Pale-tailed Barbthroat, Threnetes leucurus ?Sooty Barbthroat, Threnetes niger ?Broad-tipped Hermit, Anopetia gounellei White-bearded Hermit, Phaethornis hispidus Tawny-bellied Hermit, Phaethornis syrmatophorus Mexican Hermit, Phaethornis mexicanus Long-billed Hermit, Phaethornis longirostris Green Hermit, Phaethornis guy White-whiskered Hermit, Phaethornis yaruqui Great-billed Hermit, Phaethornis malaris Long-tailed Hermit, Phaethornis superciliosus Straight-billed Hermit, Phaethornis bourcieri Koepcke’s Hermit, Phaethornis koepckeae Needle-billed Hermit, Phaethornis philippii Buﬀ-bellied Hermit, Phaethornis subochraceus Scale-throated Hermit, Phaethornis eurynome Sooty-capped Hermit, Phaethornis augusti Planalto Hermit, Phaethornis pretrei Pale-bellied Hermit, Phaethornis anthophilus Stripe-throated Hermit, Phaethornis striigularis Gray-chinned Hermit, Phaethornis griseogularis Black-throated Hermit, Phaethornis atrimentalis Reddish Hermit, Phaethornis ruber ?White-browed Hermit, Phaethornis stuarti ?Dusky-throated Hermit, Phaethornis squalidus Streak-throated Hermit, Phaethornis rupurumii Cinnamon-throated Hermit, Phaethornis nattereri Little Hermit, Phaethornis longuemareus ?Tapajos Hermit, Phaethornis aethopygus ?Minute Hermit, Phaethornis idaliae Polytminae: Mangos Lesbiini: Coquettes Lesbiinae Coeligenini: Brilliants Patagonini: Giant Hummingbird Lampornithini: Mountain-Gems Tro chilinae Mellisugini: Bees Cynanthini: Emeralds Trochilini: Amazilias Source: McGuire et al. (2014)..

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A Giant Hummingbird from Paramo De Chingaza, Colombia.-On 10 October 1981, During an Ornithological Survey at 3250 M Elev
GENERAL NOTES 661 E. nigrivestis is timed to coincide with flowering of P. huigrensis (and other plants) which bloom seasonally at lower elevations. The general ecology of E. nigrivestis is similar to that recorded for the closely related species, the Glowing Puffleg (E. vextitus)(Snow and Snow 1980). Snow and Snow (1980) observed E. vestitus feeding principally at plants of similar general morphology (straight tubular corollas 10-20 mm in length) in similar taxonomic groups (Cnvenclishia; Ericaceae more often than Palicourea; Rubiaceae for E. vestitus). Territoriality in E. vestitus was pronounced while this was only suggested in the male E. nigrivestis we observed, perhaps a seasonal effect. Finally E. vestitus, like E. nigrivestis, did not occur in tall forested habitats at similar elevations (Snow and Snow [1980] study at 2400-2500 m). The evidence presented here suggests that the greatly restricted range of E. nigrivestis is not due to dietary specializations. Male nectar sources are from a broad spectrum of plants, and the principal food plant of both sexes, P. huigrensis, is a widespread Andean species. Nesting requirements of E. nigrivestis may still be threatened with extinction through habitat destruction, especially if the species requires specific habitats of natural vegetation at certain times of year, such as that found on nude ridge crests. The vegetation on nudes in particular is rapidly disappearing because nudes provide flat ground for cultivation in otherwise pre- cipitous terrain. In light of its restricted range and the threat of habitat destruction resulting from such close proximity to a major urban center, Quito, we consider E.
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Gene Duplication and the Evolution of Hemoglobin Isoform Differentiation in Birds
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by DigitalCommons@University of Nebraska University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Jay F. Storz Publications Papers in the Biological Sciences 11-2012 Gene Duplication and the Evolution of Hemoglobin Isoform Differentiation in Birds Michael T. Grispo University of Nebraska-Lincoln, [email protected] Chandrasekhar Natarajan University of Nebraska-Lincoln, [email protected] Joana Projecto-Garcia University of Nebraska–Lincoln Hideaki Moriyama University of Nebraska-Lincoln, [email protected] Roy E. Weber Aarhus University, Denmark See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/bioscistorz Grispo, Michael T.; Natarajan, Chandrasekhar; Projecto-Garcia, Joana; Moriyama, Hideaki; Weber, Roy E.; and Storz, Jay F., "Gene Duplication and the Evolution of Hemoglobin Isoform Differentiation in Birds" (2012). Jay F. Storz Publications. 61. https://digitalcommons.unl.edu/bioscistorz/61 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Jay F. Storz Publications by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Authors Michael T. Grispo, Chandrasekhar Natarajan, Joana Projecto-Garcia, Hideaki Moriyama, Roy E. Weber, and Jay F. Storz This article is available at DigitalCommons@University of Nebraska - Lincoln: https://digitalcommons.unl.edu/ bioscistorz/61 Published in Journal of Biological Chemistry 287:45 (November 2, 2012), pp. 37647-37658; doi: 10.1074/jbc.M112.375600 Copyright © 2012 The American Society for Biochemistry and Molecular Biology, Inc.
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Ecography ECOG-01538 Maglianesi, M
Ecography ECOG-01538 Maglianesi, M. A., Blüthgen, N., Böhning-Gaese, K. and Schleuning, M. 2015. Topographic microclimates drive microhabitat associations at the range margin of a butterfly. – Ecography doi: 10.1111/ecog.01538 Supplementary material Appendix 1 Table A1. List of families, genera and species of plants recorded by identification of pollen loads carried by hummingbird individuals at three elevations in northeastern Costa Rica. Only plant morphotypes that could be identified to species, genus or family level are given. The proportion of pollen identified to species level was 43% and that identified to a higher taxonomic level was 10%; 47% of pollen grains were categorized into pollen morphotypes (not shown here). Plant families are ordered alphabetically within each elevation. Elevation Family Genus Species Low Bromeliaceae Aechmea Aechmea mariareginae Low Acanthaceae Aphelandra Aphelandra storkii Low Bignoniaceae Arrabidaea Arrabidaea verrucosa Low Gesneraciae Besleria Besleria columnoides Low Alstroemeriaceae Bomarea Bomarea obovata Low Gesneriaceae Columnea Columnea linearis Low Gesneraceae Columnea Columnea nicaraguensis Low Gesneraceae Columnea Columnea purpurata Low Gesneraceae Columnea Columnea querceti Low Costaceae Costus Costus pulverulentus Low Costaceae Costus Costus scaber Low Costaceae Costus Costus sp 1 Low Gesneriaceae Drymonia Drymonia macrophylla Low Ericaceae Ericaceae Ericaceae 1 Low Ericaceae Ericaceae Ericaceae 2 Low Bromeliaceae Guzmania Guzmania monostachia Low Rubiaceae Hamelia Hamelia patens Low Heliconiaceae
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NESTING BEHAVIOR OF REDDISH HERMITS (PHAETHORNIS RUBER) AND OCCURRENCE OF WASP CELLS IN NESTS YOSHIKA ONIKI REDraSHHermits (Phaethornisruber) are small hummingbirdsof the forested tropical lowlands east of the Andes and south of the Orinoco (Meyer de Schauensee,1966: 161). Five birds mist-nettedat Belem (1 ø 28' S, 48ø 27' W, altitude 13 m) weighed2.0 to 2.5 g (average2.24 g). I studiedtheir nestingfrom 14 October1966 to October1967 at Belem, Brazil, in the Area de PesquisasEco16gicas do Guam•t (APEG) and MocamboForest reserves,in the Instituto de Pesquisase Experimentaqfio Agropecu•triasdo Norte (IPEAN). Names of forest types used and the Portugueseequivalents are: tidal swamp forest (vdrze'a), mature upland forest (terra-/irme) and secondgrowth (capoeira). In all casescapo.eira has been in mature upland situations. At Belem Phaethornisruber is commonall year in the lower levels of secondgrowth (capoeira) where thin branchesare plentiful. Isolated males call frequently from thin horizontal branches,never higher than 2.5-3.0 m. The male sits erect and wags his tail forward and backward as he squeaksa seriesof insectlike"pi-pi-pipipipipipi" notes, 18-20 times per minute; the first two or three notesare short and separated,the rest are run togetherrapidly. The bird sometimesstops calling for someseconds and flasheshis tongue in and out several times during the interval. I foundno singingassemblies of malehermits such as Davis (1934) describes for both the Reddishand Long-tailedHermits (Phaethornissuperciliosus). and Snow (1968) for the Little Hermit (P. longuemareus). Breeding season.--The monthly rainfall at Belem in the year of the study was 350 to 550 mm from January to May and 25 to 200 mm from June to December,with lows in October and November and highs in March and April.
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Colombia Mega II 1St – 30Th November 2016 (30 Days) Trip Report
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Special Publications Museum of Texas Tech University Number xx76 19xx January XXXX 20212010 Hummingbird (Family Trochilidae) Research: Welfare-conscious Study Techniques for Live Hummingbirds and Processing of Hummingbird Specimens Lisa A. Tell, Jenny A. Hazlehurst, Ruta R. Bandivadekar, Jennifer C. Brown, Austin R. Spence, Donald R. Powers, Dalen W. Agnew, Leslie W. Woods, and Andrew Engilis, Jr. Dedications To Sandra Ogletree, who was an exceptional friend and colleague. Her love for family, friends, and birds inspired us all. May her smile and laughter leave a lasting impression of time spent with her and an indelible footprint in our hearts. To my parents, sister, husband, and children. Thank you for all of your love and unconditional support. To my friends and mentors, Drs. Mitchell Bush, Scott Citino, John Pascoe and Bill Lasley. Thank you for your endless encouragement and for always believing in me. ~ Lisa A. Tell Front cover: Photographic images illustrating various aspects of hummingbird research. Images provided courtesy of Don M. Preisler with the exception of the top right image (courtesy of Dr. Lynda Goff). SPECIAL PUBLICATIONS Museum of Texas Tech University Number 76 Hummingbird (Family Trochilidae) Research: Welfare- conscious Study Techniques for Live Hummingbirds and Processing of Hummingbird Specimens Lisa A. Tell, Jenny A. Hazlehurst, Ruta R. Bandivadekar, Jennifer C. Brown, Austin R. Spence, Donald R. Powers, Dalen W. Agnew, Leslie W. Woods, and Andrew Engilis, Jr. Layout and Design: Lisa Bradley Cover Design: Lisa A. Tell and Don M. Preisler Production Editor: Lisa Bradley Copyright 2021, Museum of Texas Tech University This publication is available free of charge in PDF format from the website of the Natural Sciences Research Laboratory, Museum of Texas Tech University (www.depts.ttu.edu/nsrl).
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Vogelliste Venezuela
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Observations of Hummingbird Feeding Behavior at Flowers of Heliconia Beckneri and H
SHORT COMMUNICATIONS ORNITOLOGIA NEOTROPICAL 18: 133–138, 2007 © The Neotropical Ornithological Society OBSERVATIONS OF HUMMINGBIRD FEEDING BEHAVIOR AT FLOWERS OF HELICONIA BECKNERI AND H. TORTUOSA IN SOUTHERN COSTA RICA Joseph Taylor1 & Stewart A. White Division of Environmental and Evolutionary Biology, Graham Kerr Building, University of Glasgow, Glasgow, CB23 6DH, UK. Observaciones de la conducta de alimentación de colibríes con flores de Heliconia beckneri y H. tortuosa en El Sur de Costa Rica. Key words: Pollination, sympatric, cloud forest, Cloudbridge Nature Reserve, Green Hermit, Phaethornis guy, Violet Sabrewing, Campylopterus hemileucurus, Green-crowned Brilliant, Heliodoxa jacula. INTRODUCTION sources in a single foraging bout (Stiles 1978). Interactions between closely related sympatric The flower preferences shown by humming- flowering plants may involve competition for birds (Trochilidae) are influenced by a com- pollinators, interspecific pollen loss and plex array of factors including their bill hybridization (e.g., Feinsinger 1987). These dimensions, body size, habitat preference and processes drive the divergence of genetically relative dominance, as influenced by age and based floral phenotypes that influence polli- sex, and how these interact with the morpho- nator assemblages and behavior. However, logical, caloric and visual properties of flow- floral convergence may be favored if the ers (e.g., Stiles 1976). increased nectar supplies and flower densities, Hummingbirds are the primary pollina- for example, increase the regularity and rate tors of most Heliconia species (Heliconiaceae) of flower visitation for all species concerned (Linhart 1973), which are medium to large (Schemske 1981). Sympatric hummingbird- clone-forming herbs that usually produce pollinated plants probably face strong selec- brightly colored floral bracts (Stiles 1975).
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Project Scientific Progress Report Study Site
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For Examiner’s Use Centre Number Candidate Number Surname Other Names Examiner’s Initials Candidate Signature Question Mark General Certificate of Education 1 Advanced Subsidiary Examination June 2012 2 3 Biology BIOL2 4 Unit 2 The variety of living organisms 5 6 Monday 21 May 2012 1.30 pm to 3.15 pm 7 8 For this paper you must have: l a ruler with millimetre measurements. 9 l a calculator. TOTAL Time allowed l 1 hour 45 minutes Instructions l Use black ink or black ball-point pen. l Fill in the boxes at the top of this page. l Answer all questions. l You must answer the questions in the spaces provided. Do not write outside the box around each page or on blank pages. l You may ask for extra paper. Extra paper must be secured to this booklet. l Do all rough work in this book. Cross through any work you do not want to be marked. Information l The maximum mark for this paper is 85. l You are expected to use a calculator, where appropriate. l The marks for questions are shown in brackets. l Quality of Written Communication will be assessed in all answers. l You will be marked on your ability to: – use good English – organise information clearly – use scientific terminology accurately. (JUN12BIOL201) WMP/Jun12/BIOL2 BIOL2 Do not write 2 outside the box Answer all questions in the spaces provided. 1 (a) Flatworms are small animals that live in water. They have no specialised gas exchange or circulatory systems. The drawing shows one type of flatworm.
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The Behavior and Ecology of Hermit Hummingbirds in the Kanaku Mountains, Guyana
THE BEHAVIOR AND ECOLOGY OF HERMIT HUMMINGBIRDS IN THE KANAKU MOUNTAINS, GUYANA. BARBARA K. SNOW OR nearly three months, 17 January to 5 April 1970, my husband and I F camped at the foot of the Kanaku Mountains in southern Guyana. Our camp was situated just inside the forest beside Karusu Creek, a tributary of Moco Moco Creek, at approximately 80 m above sea level. The period of our visit was the end of the main dry season which in this part of Guyana lasts approximately from September or October to April or May. Although we were both mainly occupied with other observations we hoped to accumulate as much information as possible on the hermit hummingbirds of the area, particularly their feeding niches, nesting and social organization. Previously, while living in Trinidad, we had studied various aspects of the behavior and biology of the three hermit hummingbirds resident there: the breeding season (D. W. Snow and B. K. Snow, 1964)) the behavior at singing assemblies of the Little Hermit (Phaethornis Zonguemareus) (D. W. Snow, 1968)) the feeding niches (B. K. Snow and D. W. Snow, 1972)) the social organization of the Hairy Hermit (Glaucis hirsuta) (B. K. Snow, 1973) and its breeding biology (D. W. Snow and B. K. Snow, 1973)) and the be- havior and breeding of the Guys’ Hermit (Phuethornis guy) (B. K. Snow, in press). A total of six hermit hummingbirds were seen in the Karusu Creek study area. Two species, Phuethornis uugusti and Phaethornis longuemureus, were extremely scarce. P. uugusti was seen feeding once, and what was presumably the same individual was trapped shortly afterwards.
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