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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. -
Molecular Evolution and Functional Characterization of the Visual Pigment Proteins of the Great Bowerbird (Chlamydera Nuchalis) and Other Vertebrates
Molecular Evolution and Functional Characterization of the Visual Pigment Proteins of the Great Bowerbird (Chlamydera nuchalis) and Other Vertebrates by Ilke van Hazel A thesis submitted in conformity with the requirements for the degree of Doctor of Philosophy Department of Ecology and Evolutionary Biology University of Toronto © Copyright by Ilke van Hazel 2012 Molecular Evolution and Functional Characterization of the Visual Pigment Proteins of the Great Bowerbird (Chlamydera nuchalis) and Other Vertebrates Ilke van Hazel Doctor of Philosophy Department of Ecology and Evolutionary Biology University of Toronto 2012 Abstract Visual pigments are light sensitive receptors in the eye that form the basis of sensory visual transduction. This thesis presents three studies that explore visual pigment proteins in vertebrates using a number of computational and experimental methods in an evolutionary framework. The objective is not only to identify, but also to experimentally investigate the functional consequences of genetic variation in vertebrate visual pigments. The focus is on great bowerbirds (Chlamydera nuchalis), which are a model system in visual ecology due to their spectacular behaviour of building and decorating courtship bowers. There are 4 chapters: Chapter 1 introduces background information on visual pigments and vision in birds. Among visual pigment types, the short-wavelength-sensitive (SWS1) pigments have garnered particular interest due to the broad spectral range among vertebrates and the importance of UV signals in communication. Chapter 2 investigates the evolutionary history of SWS1 in vertebrates with a view toward its utility as a phylogenetic marker. Chapter 3 investigates SWS1 evolution and short-wavelength vision in birds, with particular focus on C. -
Miscellaneous Notes on the Bowerbirds Chlamydera Cerviniventris and C
AUSTRALIAN 6 BIRD WATCHER AUSTRALIAN BIRD WATCHER 1989, 13, 6-19 Miscellaneous Notes on the Bowerbirds Chlamydera cerviniventris and C. lauterbachi (Ptilonorhynchidae) in Papua New Guinea by C.B. FRITH and D.W. FRITH 'Prionodura', Paluma via Townsville, Queensland 4816 Summary Nests, a nestling and three bowers of the Fawn-breasted Bowerbird Chlamydera cerviniventris are described, and observations of parental nest attendance reported. Nests, eggs and bowers of Lauterbach's Bowerbird C. lauterbachi are described and observations of male and female behaviours at a bower reported. First descriptions of nestling, fledgling and juvenile Lauterbach's Bowerbird are given. The location of nests relative to bowers and seasonality of nesting of the Fawn-breasted and Lauterbach's Bowerbirds are reviewed. Introduction The four or five Chlamydera bowerbird species (Ptilonorhynchidae) are unlike the other fourteen, forest-dwelling, species in that they inhabit only open drier habitats of riverine forests, open woodlands, grasslands and adjacent forest edges (Donaghey et al. 1985). They are all members of the 'avenue' bower building group but differ from Sericulus and Ptilonorhynchus species, in which males are brightly coloured, by being dull and cryptically sexually monomorphic or very nearly so (Gilliard 1969). Least known of the Chlamydera species are Lauterbach's Bowerbird C. lauterbachi endemic to central and north-eastern New Guinea, and the Fawn-breasted Bowerbird C. cerviniventris of north-western Cape York Peninsula, Australia, and coastal central and eastern New Guinea and the eastern Vogelkop (Cooper & Forshaw 1W7) . Other than descriptions of bowers, some male displays and nest and eggs, little is known of nesting habits and nest dispersion relative to bower locations in Lauterbach's and Fawn-breasted Bowerbirds (Peckover 1969, Cooper & Forshaw 1W7). -
Birds of New Guinea Field Guide (Beehler Et Al
© Copyright, Princeton University Press. No part of this book may be distributed, posted, or reproduced in any form by digital or mechanical means without prior written permission of the publisher. Introduction The New Guinea Region Our region of coverage follows Mayr (1941: vi), who defined the natural region that encompasses the avifauna of New Guinea, naming it the “New Guinea Region.” It comprises the great tropical island of New Guinea as well as an array of islands lying on its continental shelf or immediately offshore. This region extends from the equator to latitude 12o south and from longitude 129o east to 155o east; it is 2,800 km long by 750 km wide and supports the largest remaining contiguous tract of old-growth humid tropical forest in the Asia-Pacific (Beehler 1993a). The Region includes the Northwestern Islands (Raja Ampat group) of the far west—Waigeo, Batanta, Salawati, Misool, Kofiau, Gam, Gebe, and Gag; the Aru Islands of the southwest—Wokam, Kobroor, Trangan, and others; the Bay Islands of Geelvink/Cenderawasih Bay—Biak-Supiori, Numfor, Mios Num, and Yapen; Dolak Island of south-central New Guinea (also known as Dolok, Kimaam, Kolepom, Yos Sudarso, or Frederik Hendrik); Daru and Kiwai Islands of eastern south-central New Guinea; islands of the north coast of Papua New Guinea (PNG)—Kairiru, Muschu, Manam, Bagabag, and Karkar; and the Southeastern (Milne Bay) Islands of the far southeast—Goodenough, Fergusson, Normanby, Kiriwina, Kaileuna, Wood- lark, Misima, Tagula/Sudest, and Rossel, plus many groups of smaller islands (see the endpapers for a graphic delimitation of the Region). -
An Inverse Relationship Between Decoration and Food Colour Preferences in Satin Bowerbirds Does Not Support the Sensory Drive Hypothesis
ANIMAL BEHAVIOUR, 2006, 72, 1125e1133 doi:10.1016/j.anbehav.2006.03.015 An inverse relationship between decoration and food colour preferences in satin bowerbirds does not support the sensory drive hypothesis GERALD BORGIA*† & JASON KEAGY† *Department of Biology, University of Maryland, College Park yDepartment of Behavior, Ecology, Evolution and Systematics Program, University of Maryland, College Park (Received 20 September 2005; initial acceptance 25 October 2005; final acceptance 30 March 2006; published online 26 September 2006; MS. number: A10246) Male bowerbirds collect and decorate their bowers with coloured objects that influence female choice. A recent version of the sensory drive hypothesis claims that female food colour preferences have driven the evolution of female preferences for the colour of male display traits. This hypothesis predicts a positive correlation between male display and food colour preferences. A positive correlation between food and decoration preferences could also arise because of sensory biases built into bowerbirds or the environment. Here we test hypotheses that (1) male and female satin bowerbirds show well-defined food colour prefer- ences, (2) these preferences correlate with independently assessed preferences for bower decorations, and, in a cross-species comparison, (3) food items were used as the first bower decorations. We found that male and female satin bowerbirds, Ptilonorhynchus violaceus, preferentially use long wavelength and were colours as food items. Male decoration preferences were biased towards colours of short wavelength and were negatively correlated with food colour preferences. Our reconstruction of ancestral character states is most consistent with the hypothesis that the original bower decorations were inedible objects and were thus unlikely to have been dual-use traits that also functioned as food items. -
Indian Myna Acridotheres Tristis Rch 2009, the Department of Primary Industries and Fisheries Was Amalgamated with Other
Invasive animal risk assessment Biosecurity Queensland Agriculture Fisheries and Department of Indian myna Acridotheres tristis Anna Markula, Martin Hannan-Jones and Steve Csurhes First published 2009 Updated 2016 rch 2009, the Department of Primary Industries and Fisheries was amalgamated with other © State of Queensland, 2016. The Queensland Government supports and encourages the dissemination and exchange of its information. The copyright in this publication is licensed under a Creative Commons Attribution 3.0 Australia (CC BY) licence. You must keep intact the copyright notice and attribute the State of Queensland as the source of the publication. Note: Some content in this publication may have different licence terms as indicated. For more information on this licence visit http://creativecommons.org/licenses/ by/3.0/au/deed.en" http://creativecommons.org/licenses/by/3.0/au/deed.en Photo: Guillaume Blanchard. Image from Wikimedia Commons under a Creative Commons Attribution ShareAlike 1.0 Licence. I n v a s i v e a n i m a l r i s k a s s e s s m e n t : Indian myna Acridotheres tristis 2 Contents Introduction 4 Name and taxonomy 4 Description 4 Biology 5 Life history 5 Social organisation 5 Diet and feeding behaviour 6 Preferred habitat 6 Predators and dieseases 7 Distribution and abundance overseas 7 Distribution and abundance in Australia 8 Species conservation status 8 Threat to human health and safety 9 History as a pest 9 Potential distribution and impact in Queensland 10 Threatened bird species 11 Threatened mammaly species 11 Non-threatened species 12 Legal status 12 Numerical risk assessment 12 References 13 Appexdix 1 16 I n v a s i v e a n i m a l r i s k a s s e s s m e n t : Indian myna Acridotheres tristis 3 Introduction Name and taxonomy Species: Acridotheres tristis Syn. -
Evolution of Colorful Display
COMMENTARY doi:10.1111/j.1558-5646.2007.00051.x EVOLUTION OF COLORFUL DISPLAY Gerald Borgia,1 Brian Coyle, and P. B. Zwiers Department of Biology, University of Maryland, College Park, Maryland 20742-4415 1E-mail: [email protected] Received February 27, 2006 Accepted November 27, 2006 How the displays of bowerbirds have evolved has attracted widespread interest. Endler et al. (2005) analyzed color use in display in a subset of bowerbird species and generalized their results to all bowerbirds. Here we discuss problems with their analysis that calls into question their conclusions. For example, they state that bowerbirds do not use decorations that match their background, but this is not supported by their results. They reconstruct historical patterns of sexual dimorphism in plumage display using questionable methodology. The high lability of these display traits makes these reconstructions unreliable and, using accepted methods and acknowledging the lability problem, we were unable to support their conclusions. Their claim that plumage differences between sympatric species are due to character displacement is not supported by the available data. Their focus is on visual contrast as the cause for display color and we offer additional hypotheses that may contribute to explaining color use. We support studies of spectral analysis of display traits but urge greater care in using this information to reach conclusions about how colorful displays have evolved. KEY WORDS: Character displacement, character-state reconstruction, mate recognition, rapid evolution, sexual selection. Bowerbirds are widely known for their multifaceted sexual dis- logeny suggest the following sequence of events: (1) increase of plays including a bower, bower decorations, and dancing and vo- contrast under sexual selection; (2) onset of increased predation cal elements. -
Tongues of Some Passerine Birds by Mrs
Vol. 6 MARCH 15, 1975 No.1 Tongues of Some Passerine Birds By Mrs. ELLEN M. McCULLOCH, Mitcham, Victoria. SUMMARY The tongues of five species, of three genera, of passerine birds are depicted, and the feeding of certain brush-tongued birds, on various types of food, placed in hanging pottery feeders, is discussed. Some previous research on brush-tongues is given. During August 1972, the Bird Observers Club arranged for the production of hanging pottery feeders, to hold either a solid food mix, or a sweet liquid "nectar", largely designed to attract honey eaters. Several hundred of these feeders are now in use, and the variation in species attracted to them has proved to be interesting. Many birds are opportune feeders and take advantage of tem porary, readily available food supplies. It was anticipated that honeyeaters, Meliphagidae, and silvereyes, Zosteropidae, would readily find the liquid in feeders, and this has generally been found to be so. Additionally, other quite unrelated species have been recorded. These include Ravens, Corvus sp., Crimson Rosella, Platycercus elegans, Striated Thornhill, Acanthiza lineata, and Superb Blue Wren, Malurus cyaneus. The tongues of ravens and rosellas do not appear to be in any way adapted, particularly to the collection of nectar, unlike those of honeyeaters and silvereyes (Rand, 1967). Examination of the tongues of the thornbill and wren showed that, in each species, the tip of the tongue is to some extent frayed out (Fig. l.a, and l.c). Gardner ( 1925), when writing about passerine birds, states: "In many families the thin horny tongue, slightly curled and frayed at the tip, as described for the robin, is found with but slight differences in length and width. -
Novitates No
AMERIICAN MUSEUM NOV ITATES PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CITY OF NEW YORK DECEMBER 12, 1952 NUMBER 1602 GEOGRAPHIC VARIATION AND PLUMAGES IN AUSTRALIAN BOWERBIRDS (PTILONORHYNCHIDAE) By ERNST MAYR AND KATE JENNINGS INTRODUCTION In view of the great recent interest in the biology of bower- birds, it is surprising how little is known about the taxonomy of the Australian species. The available accounts in the standard works are very confusing, since no difference is made in most of them between synonyms and valid subspecies. Furthermore, a study of individual variation, of the sequence of plumages, and of measurements is badly needed, as information on these matters is woefully inadequate in the existing literature. In fact, we know much more about the New Guinea species than about the most familiar Australian birds. The following account is based on the material in the American Museum of Natural History which includes the Rothschild and Mathews collections. Where this material proved inadequate, additional specimens were borrowed from the United States National Museum, the Chicago Natural History Museum, the Museum of Comparative Zoology, and the Academy of Natural Sciences of Philadelphia (including parts of the Gould Collec- tion). We greatly appreciate the kindness of the curators of these institutions in making this material available. Ailuroedus crassirostris Paykull GREEN CATBIRD The only two Australian subspecies of this Australo-Papuan species are so different from each other that they were listed as 2 AMERICAN MUSEUM NOVITATES NO. 1602 two species in most of the older literature. However, their essential similarity, the agreement of habits, and the basic dif- ference from buccoides (New Guinea), the only other species of the genus, make it evident that crassirostris Paykull, 1815 (=viridis Vieillot, 1817), and maculosus Ramsay, 1875, must be considered as conspecific. -
Description of .A Ne~. Subspecies of Climacteris
De.~cription. of a Ne.w S1~bspecies of Olimact6ris. 5-,, ' ' , • . I . Description of .a Ne~. Subspecies of Climacteris. ·By J. W. Mellor, ,R.A.O.U. Olimacteris eryth1·ops .parsonsi subsp., nov. Mellor. Southevn White-browed Treecreeper. · Type .locality 'Pungonda, Hundred of Bookpurnong7 l;:!outh Australia. · . · . : As might reasonably );le ·expected a climacteris inhabit ing: the pine ann mallee country of the River Murray would! diffet~ con~derably from. its ally of the arid districts of Cen tral Australia. When comparing the 'skins of a pair of the. white-browed treecreepers that I procured from Pungonda in the Hundred of Bookpurnong, S.A., in October last, with North's description of the White-browed Treecreeper procured by the Horn Expedition to. Central Australia, vide report of Horn Expedition, Aves p. 96 I found the following differences: The Soutl;l.ern form is altogether more robust1 and the coloration differs considerably from the Central Aus tralian bird~ being more greyish a;bove; crown of head and forehead being uniform dark grey; no wa:sh of brown on ~he· grey upper tail cove1,·'ts; subterminal band on tail black; no bu:ffy brown on sides of body and centre of abdlomen; and dull white in place of buffy white on under tail yoverts, ·which are ''barred" "\"\<ith black spots. The :birds were rare7 ~I .fi Description of a New Snbspeci~s of OlimacteJ'l:s. ---- .and very noisele·ss, being in marked contrast to the Soutliern Brown Treecreeper (Cflimacteris picum111Us australis) Mathews, •with which they were in companY, I propose to designate the bird in the vernacular lis:t as the S.outhern White-browed Treecreeper, and scientifically ·a:s Olimacteris erythrops 1parsonsi, in ·honour of Mr. -
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, -
The Hidden Crisis of Animal Welfare in Queensland CONTENTS EXECUTIVE SUMMARY 4 1
THIS REPORT HAS BEEN PRODUCED IN COLLABORATION WITH Tree-clearing: the hidden crisis of animal welfare in Queensland CONTENTS EXECUTIVE SUMMARY 4 1. INTRODUCTION 7 Rising habitat destruction 8 2. LIVES LOST 10 Animal at risk 12 Mammals 12 About the authors Dr Martin Taylor is a conservation scientist with Birds 13 over two decades of international experience in endangered species and conservation research and Reptiles and frogs 14 advocacy. Aquatic animals 14 He has served on the scientific committee of the International Whaling Commission, and Animals Committee of CITES. 3. IMPACTS ON WILDLIFE WELFARE 15 He is a member of the IUCN World Commission Wild animal fates after tree-clearing 15 on Protected Areas. Dr Taylor currently serves as principal conservation scientist with WWF- Afflictions and injuries 18 Australia. Dr Carol Booth is a writer, naturalist, Wildlife rescue, rehabilitation and release 20 environmental philosopher, and policy advisor. Case study: Koalas in southeast Queensland 22 She has worked as an advocate on a wide range of conservation issues, including protecting flying- foxes, strengthening environmental biosecurity and 4. REDUCING IMPACTS 23 improving water laws. She was editor of Wildlife Australia, and has written numerous conservation Wildlife salvage 23 reports and articles. Wildlife rescue 25 Dr Mandy Paterson is a Veterinarian and Principal Scientist at RSCPA Queensland, with decades of experience in animal science research and 5. GAPS IN LEGAL PROTECTION 26 advocacy. Dr Paterson also serves on several boards and committees dealing with animal welfare such Vegetation Management Act 1999 27 as the round-table on the spotter/catcher code and the Centre for Animal Welfare and Ethics Advisory Nature Conservation Act 1992 28 Committee.