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Photographic Evidence of Nectar-Feeding by the White-Throated Treecreeper Cormobates Leucophaea
103 AUSTRALIAN FIELD ORNITHOLOGY 2009, 26, 103–104 A White-throated Treecreeper feeding upon the nectar of Umbrella Tree flowers by tongue lapping, near Malanda, north Qld Plate 17 Photo: Clifford B. Frith Photographic Evidence of Nectar-feeding by the White-throated Treecreeper Cormobates leucophaea CLIFFORD B. FRITH P.O. Box 581, Malanda, Queensland 4885 (Email: [email protected]) Summary. An individual of the north-eastern Australian subspecies of the White-throated Treecreeper Cormobates leucophaea minor was closely observed and photographed while clearly feeding upon nectar from the flowers of an Umbrella Tree Schefflera actinophylla. Although the few other records of nectar-feeding by treecreepers (Family Climacteridae) are reviewed, this note presents the first substantiated evidence of nectar-feeding by Australasian treecreepers. The most recent review of the biology of the Family Climacteridae as a whole described treecreepers as taking nectar from flowers at times (Noske 2007). However, few published records of nectar-feeding by any of the six Australian treecreeper species exist. Of the five species of the genus Climacteris, only one (the Brown Treecreeper C. picumnus) is known to occasionally drink nectar from ironbarks such as Mugga Eucalyptus sideroxylon (V. & E. Doerr, cited in Higgins et al. 2001) and from paperbarks (Orenstein 1977). The Black-tailed Treecreeper C. melanura has been observed feeding on the Banksia-like inflorescences of the FRITH: AUSTRALIAN 104 White-throated Treecreeper Eating Nectar FIELD ORNITHOLOGY Bridal Tree Xanthostemon paradoxus, another myrtaceous species (R. Noske pers. comm.). The White-throated Treecreeper Cormobates leucophaea was recently described as ‘Almost wholly insectivorous, mainly bark-dwelling ants; occasionally take some plant material’ (Higgins et al. -
Special Issue3.7 MB
Volume Eleven Conservation Science 2016 Western Australia Review and synthesis of knowledge of insular ecology, with emphasis on the islands of Western Australia IAN ABBOTT and ALLAN WILLS i TABLE OF CONTENTS Page ABSTRACT 1 INTRODUCTION 2 METHODS 17 Data sources 17 Personal knowledge 17 Assumptions 17 Nomenclatural conventions 17 PRELIMINARY 18 Concepts and definitions 18 Island nomenclature 18 Scope 20 INSULAR FEATURES AND THE ISLAND SYNDROME 20 Physical description 20 Biological description 23 Reduced species richness 23 Occurrence of endemic species or subspecies 23 Occurrence of unique ecosystems 27 Species characteristic of WA islands 27 Hyperabundance 30 Habitat changes 31 Behavioural changes 32 Morphological changes 33 Changes in niches 35 Genetic changes 35 CONCEPTUAL FRAMEWORK 36 Degree of exposure to wave action and salt spray 36 Normal exposure 36 Extreme exposure and tidal surge 40 Substrate 41 Topographic variation 42 Maximum elevation 43 Climate 44 Number and extent of vegetation and other types of habitat present 45 Degree of isolation from the nearest source area 49 History: Time since separation (or formation) 52 Planar area 54 Presence of breeding seals, seabirds, and turtles 59 Presence of Indigenous people 60 Activities of Europeans 63 Sampling completeness and comparability 81 Ecological interactions 83 Coups de foudres 94 LINKAGES BETWEEN THE 15 FACTORS 94 ii THE TRANSITION FROM MAINLAND TO ISLAND: KNOWNS; KNOWN UNKNOWNS; AND UNKNOWN UNKNOWNS 96 SPECIES TURNOVER 99 Landbird species 100 Seabird species 108 Waterbird -
Supplementary Information For
Supplementary Information for Earth history and the passerine superradiation Oliveros, Carl H., Daniel J. Field, Daniel T. Ksepka, F. Keith Barker, Alexandre Aleixo, Michael J. Andersen, Per Alström, Brett W. Benz, Edward L. Braun, Michael J. Braun, Gustavo A. Bravo, Robb T. Brumfield, R. Terry Chesser, Santiago Claramunt, Joel Cracraft, Andrés M. Cuervo, Elizabeth P. Derryberry, Travis C. Glenn, Michael G. Harvey, Peter A. Hosner, Leo Joseph, Rebecca Kimball, Andrew L. Mack, Colin M. Miskelly, A. Townsend Peterson, Mark B. Robbins, Frederick H. Sheldon, Luís Fábio Silveira, Brian T. Smith, Noor D. White, Robert G. Moyle, Brant C. Faircloth Corresponding authors: Carl H. Oliveros, Email: [email protected] Brant C. Faircloth, Email: [email protected] This PDF file includes: Supplementary text Figs. S1 to S10 Table S1 to S3 References for SI reference citations Other supplementary materials for this manuscript include the following: Supplementary Files S1 to S3 1 www.pnas.org/cgi/doi/10.1073/pnas.1813206116 Supplementary Information Text Extended Materials and Methods Library preparation and sequencing. We extracted and purified DNA from fresh muscle tissue, liver tissue, or toepad clips from 113 vouchered museum specimens (Supplementary File S1) using the Qiagen DNeasy Blood and Tissue Kit following the manufacturer’s protocol. We quantified DNA extracts using a Qubit fluorometer, and we prepared aliquots of DNA extracted from muscle and liver at 10 ng/µL in 60 µL volume for shearing. We sheared each DNA sample to 400–600 bp using a Qsonica Q800R sonicator for 15–45 cycles, with each cycle running for 20 seconds on and 20 seconds off at 25% amplitude. -
Final Report Melaleuca Wetlands, Coochiemudlo Island, Fauna Survey 2016 Ronda J Green, Bsc (Hons) Phd
Final Report Melaleuca Wetlands, Coochiemudlo Island, Fauna Survey 2016 Ronda J Green, BSc (Hons) PhD for Coochiemudlo Island Coastcare Supported by Redland City Council Acknowledgements I would like to express thanks to Redland City Council for financial and other support and to Coochiemudlo Island Coastcare for opportunity to conduct the survey, accommodation for Darren and myself, and many kinds of support throughout the process, including the sharing of photos and reports of sightings by others. Volunteers provided invaluable assistance in carrying traps and tools, setting and checking traps, digging holes for pitfall traps and setting associated drift nets, looking for animals on morning and nocturnal searches, collecting and washing traps after the surveys and assisting in other ways. Volunteers were (in alphabetical order): Elissa Brooker, Nikki Cornwall, Raymonde de Lathouder, Lindsay Duncan, Ashley Edwards, Kurt Gaskill, Diane Gilham, Deb Hancox, Margrit Lack, Chris Leonard, Susan Meek, Leigh Purdie, Natascha Quadt, Narelle Renn, Lu Richards, Graeme Roberts-Thomson, Vivienne Roberts-Thomson, Charlie Tomsin, and Bruce Wollstein Thanks also to Carolyn Brammer and Lindsay Duncan for allowing volunteers the use their cabin accommodation for at-cost rates each of the four seasons. Thanks again to Coastcare for providing a number of BBQ's, other meals, tea, coffee and muffins for ourselves and volunteers. Thanks also to Alexandra Beresford and Tim Herse for setting up additional motion-sensing camera, and to Scenic Rim Wildlife for allowing us to borrow theirs. Finally we would like to thank Steve Willson and Patrick Couper of the Queensland Museum for assistance with identification of a snake and a frog. -
Earth History and the Passerine Superradiation
Earth history and the passerine superradiation Carl H. Oliverosa,1, Daniel J. Fieldb,c, Daniel T. Ksepkad, F. Keith Barkere,f, Alexandre Aleixog, Michael J. Andersenh,i, Per Alströmj,k,l, Brett W. Benzm,n,o, Edward L. Braunp, Michael J. Braunq,r, Gustavo A. Bravos,t,u, Robb T. Brumfielda,v, R. Terry Chesserw, Santiago Claramuntx,y, Joel Cracraftm, Andrés M. Cuervoz, Elizabeth P. Derryberryaa, Travis C. Glennbb, Michael G. Harveyaa, Peter A. Hosnerq,cc, Leo Josephdd, Rebecca T. Kimballp, Andrew L. Mackee, Colin M. Miskellyff, A. Townsend Petersongg, Mark B. Robbinsgg, Frederick H. Sheldona,v, Luís Fábio Silveirau, Brian Tilston Smithm, Noor D. Whiteq,r, Robert G. Moylegg, and Brant C. Fairclotha,v,1 aDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803; bDepartment of Biology & Biochemistry, Milner Centre for Evolution, University of Bath, Claverton Down, Bath BA2 7AY, United Kingdom; cDepartment of Earth Sciences, University of Cambridge, Cambridge CB2 3EQ, United Kingdom; dBruce Museum, Greenwich, CT 06830; eDepartment of Ecology, Evolution and Behavior, University of Minnesota, Saint Paul, MN 55108; fBell Museum of Natural History, University of Minnesota, Saint Paul, MN 55108; gDepartment of Zoology, Museu Paraense Emílio Goeldi, São Braz, 66040170 Belém, PA, Brazil; hDepartment of Biology, University of New Mexico, Albuquerque, NM 87131; iMuseum of Southwestern Biology, University of New Mexico, Albuquerque, NM 87131; jDepartment of Ecology and Genetics, Animal Ecology, Evolutionary Biology Centre, -
Or POLYMYODI): Oscines (Songbirds
Text extracted from Gill B.J.; Bell, B.D.; Chambers, G.K.; Medway, D.G.; Palma, R.L.; Scofield, R.P.; Tennyson, A.J.D.; Worthy, T.H. 2010. Checklist of the birds of New Zealand, Norfolk and Macquarie Islands, and the Ross Dependency, Antarctica. 4th edition. Wellington, Te Papa Press and Ornithological Society of New Zealand. Pages 275, 279-280 & 299-300. Order PASSERIFORMES: Passerine (Perching) Birds See Christidis & Boles (2008) for a review of recent studies relevant to the higher-level systematics of the passerine birds. Suborder PASSERES (or POLYMYODI): Oscines (Songbirds) The arrangement of songbirds in the 1970 Checklist (Checklist Committee 1970) was based on the premise that the species endemic to the Australasian region were derived directly from Eurasian groups and belonged in Old World families (e.g. Gerygone and Petroica in Muscicapidae). The 1990 Checklist (Checklist Committee 1990) followed the Australian lead in allocating various native songbirds to their own Australasian families (e.g. Gerygone to Acanthizidae, and Petroica to Eopsaltriidae), but the sequence was still based largely on the old Peters-Mayr arrangement. Since the late 1980s, when the 1990 Checklist was finalised, evidence from molecular biology, especially DNA studies, has shown that most of the Australian and New Zealand endemic songbirds are the product of a major Australasian radiation parallel to the radiation of songbirds in Eurasia and elsewhere. Many superficial morphological and ecological similarities between Australasian and Eurasian songbirds are the result of convergent evolution. Sibley & Ahlquist (1985, 1990) and Sibley et al. (1988) recognised a division of the songbirds into two groups which were called Corvida and Passerida (Sibley & Ahlquist 1990). -
To Download the PDF File
The effects of species behavioural responses to roads and life history traits on their population level responses to roads by Trina Rytwinski A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology Carleton University Ottawa, Ontario ©2012 Trina Rytwinski Library and Archives Bibliotheque et Canada Archives Canada Published Heritage Direction du 1+1 Branch Patrimoine de I'edition 395 Wellington Street 395, rue Wellington Ottawa ON K1A0N4 Ottawa ON K1A 0N4 Canada Canada Your file Votre reference ISBN: 978-0-494-93680-1 Our file Notre reference ISBN: 978-0-494-93680-1 NOTICE: AVIS: The author has granted a non L'auteur a accorde une licence non exclusive exclusive license allowing Library and permettant a la Bibliotheque et Archives Archives Canada to reproduce, Canada de reproduire, publier, archiver, publish, archive, preserve, conserve, sauvegarder, conserver, transmettre au public communicate to the public by par telecommunication ou par I'lnternet, preter, telecommunication or on the Internet, distribuer et vendre des theses partout dans le loan, distrbute and sell theses monde, a des fins commerciales ou autres, sur worldwide, for commercial or non support microforme, papier, electronique et/ou commercial purposes, in microform, autres formats. paper, electronic and/or any other formats. The author retains copyright L'auteur conserve la propriete du droit d'auteur ownership and moral rights in this et des droits moraux qui protege cette these. Ni thesis. Neither the thesis nor la these ni des extraits substantiels de celle-ci substantial extracts from it may be ne doivent etre imprimes ou autrement printed or otherwise reproduced reproduits sans son autorisation. -
AC28 Doc. 21.2
Original language: English AC28 Doc. 21.2 CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ___________________ Twenty-eighth meeting of the Animals Committee Tel Aviv (Israel), 30 August-3 September 2015 Interpretation and implementation of the convention Species trade and conservation Standard nomenclature REVISED NOMENCLATURE FOR FOUR SPECIES OF BIRDS-OF-PARADISE (PARADISAEIDAE) 1. This document has been submitted by the United States of America.1 2. On March 25, 2015 the Ornithological Council (OC), a non-governmental organization in the United States, requested that the United States recommend changes to the taxonomy/nomenclature for four species found in the birds-of-paradise (Paradisaeidae) family. These nomenclature changes would no longer place these four bird species in the Paradisaeidae family. 3. The species are: Macgregor’s bird-of-paradise (Macgregoria pulchra), Loria’s bird-of-paradise or Loria’s cnemophilus (Cnemophilus loriae), the Crested bird-of-paradise or crested cnemophilus (Cnemophilus macgregorii), and the yellow-breasted bird-of-paradise or yellow-breasted cnemophilus (Loboparadisea sericea). The first three species occur in Indonesia and Papua New Guinea, while the Crested bird-of- paradise or yellow-breasted cnemophilus occurs only in Papua New Guinea. 4. The recommended new taxonomy would place Macgregor’s Bird of Paradise in the Meliphagidae family (Honeyeaters), and the other three species in the Cnemophilidae family (Satinbirds). 5. The standard CITES nomenclature for the species included in the family Paradiseidae is : Morony, J.J., Bock, W.J. & Farrand, J., Jr. (1975): Reference List of the Birds of the World. American Museum of Natural History. -
Aprasiainis87 FAMILY
61 GENUS: Oedura GENUS; Lygodactylus GENUS: Phyllurus GENUS: Matoatoa GENUS: Pseudothecadactyl us GENUS: Microscalabotes* GENUS: Rhacodactylus GENUS; Nactus GENUS: Rhynchoedura* GENUS: Narudasia* GENUS: SaItuarius GENUS: Pachydactylus GENUS: Underwoodisaurus GENUS; PaImatogecko SUBFAMILY: Eublepbarinae'" GENUS; Psragehyra GENUS: Coleonyx GENUS: Psroedura GENUS: Eublepbaris GENUS; Perochirus GENUS: Goniurosaurus GENUS: Phelsuma GENUS: Hemitheconyx GENUS: Phyllodactylus GENUS: Holodactylus GENUS; Phyllopezus SUBFAMILY: Gekkoninae GENUS: Pristurus GENUS: Afroedura GENUS; Pseudogekko GENUS: Afrogecko GENUS; Pseudogonatodes GENUS: Agamura GENUS: Plenopus GENUS: Ailuronyx GENUS: Plychozoon GENUS: Alsophylax GENUS; Plyodactylus GENUS; Arlstelliger GENUS: Quedenfeldtia GENUS; Asaccus GENUS: Rhoptropus GENUS; Blaesodactylus GENUS; Saurodactylus GENUS: Bogertia* GENUS: Sphaerodactylus GENUS; Brlha* GENUS; Stenodactylus GENUS: Bunopus GENUS; Tarentola GENUS: Calodactylodes GENUS; Teratolepis GENUS: Carinatogecko GENUS; Thecadactylus* GENUS: Chondrodactyiu,* GENUS: Tropiocoiotes GENUS; Christinus GENUS; Urocotyledon GENUS: Cnemaspis GENUS: Uroplatus GENUS; Coleodactylus SUBFAMILY: Teratoscincinae GENUS; Colopus* GENUS: Teratoscincus GENUS: Cosymbotus FAMILY: Pygopodidae'" GENUS: Crossobamon SUBFAMILY: LiaIisinae GENUS: Cryptactites' TRIBE: Aprasiaini S87 GENUS; Cyrtodactylus GENUS; J\prasia GENUS: Cyrtopodion GENUS: Ophidiocephalus* GENUS: Dixonius GENUS; Pletholax* GENUS: Dravidogecko* TRIBE: Lialisini GENUS; Ebenavia GENUS: LiaIis GENUS; EuIeptes* -
Nest Ecology of a Threatened Woodland Avifauna
Nest Ecology of a Threatened Woodland Avifauna Graham R. FULTON B.Sc. (Syd). Hons. (UNE). Macleay Miklouho-Maclay Centenary Research Fellow (Syd). Willie Wagtail Rhipidura leucophrys nestlings just prior to fledging A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2019 School of Biological Sciences ABSTRACT The vast clearing of temperate eucalypt woodland and forest for agriculture in Australia has led to the concomitant decline of its biota. This thesis investigated the nest ecology of this disappearing landscape’s threatened avifauna to obtain baseline/life-history data to support the avifauna’s conservation and inform evolutionary theory. The nesting ecology of this avifauna was reviewed both qualitatively and quantitatively. Field data were collected from a large 27,000 ha woodland with ecologically functional numbers of birds and where invasive species were controlled. This woodland, Dryandra, is located within a region (in south-western Australia) where up to 97% of the native woodland vegetation has been removed. Despite this Dryandra’s avifauna has increased in abundance since the 1950s. An Australia-wide review and a meta-analyses established the identity of 94 nests predators in temperate forest and woodland and identified important metrics and trends, such as: mesopredators being found to iteratively replace one another as larger species were removed; artificial nests were concluded, at best, to be generators of hypotheses to be tested at natural nests; edge-effects were equivocal and thus fragment size, structure and faunal assemblage set in a more complex paradigm were considered more appropriate in explaining differences in nest predation; and, the various types of evidence used to identify nest predators were considered with cameras deemed the most functional and direct observations the most informative. -
Bulletin of the British Ornithologists' Club
Bulletin of the British Ornithologists’ Club Volume 141 No. 1 (Online) ISSN 2513-9894 (Online) March 2021 Bulletin of the British Ornithologists’ Club ISSN 2513-9894 (Online) Edited by Guy M. Kirwan Associate Editors: Robert Prŷs-Jones; Lincoln Fishpool Volume 141 Number 1, pages 1–116 CONTENTS Club Announcements ........................................................................................................................................... 1 MORRIS, P. A reassessment of issues surrounding the Hastings Rarities, with particular reference to supposed fraud by George Bristow........................................................................................................ 3 MARAIS, E., PEACOCK, F. & ALLPORT, G. First record of Forbes-Watson’s Swift Apus berliozi in southern Africa, with comments on vocal and visual identification ................................................ 21 WILSON, J.-J. Birds from Sumatra given by Sir Stamford Raffles to Lord Stanley: links to names, types and drawings .................................................................................................................................................. 39 DAVID, N., ELLIOTT, A. & BRUCE, M. D. The valid specific name of Sulawesi’s Maroon-chinned Fruit Dove: gularis Quoy & Gaimard, 1832 ................................................................................................ 50 ROUND, P. D., PROMNUN, P., MANAWATTANA, S. & JAHAN, I. Non-breeding season records of the Alpine Leaf Warbler Phylloscopus occisinensis .................................................................. -
Conservation Ecology and Breeding Biology of the White-Browed Treecreeper Climacteris Affinis
Conservation Ecology and Breeding Biology of the White-browed Treecreeper Climacteris affinis James Radford B.Sc. (Hons) University of Melbourne A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy of Deakin University June 2002 Acknowledgments First and foremost, I would like to thank my supervisor, Andrew Bennett, for his tireless encouragement, enthusiasm, direction and wisdom throughout my candidature. Your door was always open and your advice re-assuring. Thanks AB. This research was possible because I was the recipient of an Australian Postgraduate Award. I would also like to acknowledge the financial assistance provided by the Department of Natural Resources and Environment (North-west region), the School of Ecology and Environment at Deakin University, Birds Australia through the auspices of the Stuart Leslie Bird Research Award, the M. A. Ingram Trust and the Society for Conservation Biology (travel award). Drs. Ralph MacNally (Monash University) and John White (Deakin University) generously offered advice on statistical analysis and other matters of research design. Chris Lewis and Rowena Scott (Deakin University) provided invaluable assistance with technical, logistical and day-to-day business and their help was greatly appreciated. Jackie MacReadie, Andrew Giles and Grant Michie ensured my administrative affairs were in order. My thanks to Charles and Joan Sandbrink, Kahlid Al-Dabbagh, and the banding team at Rushworth for their assistance with my bird-banding training. I received great support and assistance from Geoffrey Allen and Victor Hurley (Flora and Fauna, NRE, Mildura). Special thanks to all the Parks Victoria staff at Werrimull and Wyperfeld, especially Lorraine Ludewigs, Peter Teasdale, Jack Kelly, Travis Harman and Brian Goldsmith.