Ecography ECOG-04863 Callaghan, C
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Lx1/Rtetcanjviuseum
lx1/rtetcanJViuseum PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK 24, N.Y. NUMBER 1707 FEBRUARY 1 9, 1955 Notes on the Birds of Northern Melanesia. 31 Passeres BY ERNST MAYR The present paper continues the revisions of birds from northern Melanesia and is devoted to the Order Passeres. The literature on the birds of this area is excessively scattered, and one of the functions of this review paper is to provide bibliographic references to recent litera- ture of the various species, in order to make it more readily available to new students. Another object of this paper, as of the previous install- ments of this series, is to indicate intraspecific trends of geographic varia- tion in the Bismarck Archipelago and the Solomon Islands and to state for each species from where it colonized northern Melanesia. Such in- formation is recorded in preparation of an eventual zoogeographic and evolutionary analysis of the bird fauna of the area. For those who are interested in specific islands, the following re- gional bibliography (covering only the more recent literature) may be of interest: BISMARCK ARCHIPELAGO Reichenow, 1899, Mitt. Zool. Mus. Berlin, vol. 1, pp. 1-106; Meyer, 1936, Die Vogel des Bismarckarchipel, Vunapope, New Britain, 55 pp. ADMIRALTY ISLANDS: Rothschild and Hartert, 1914, Novitates Zool., vol. 21, pp. 281-298; Ripley, 1947, Jour. Washington Acad. Sci., vol. 37, pp. 98-102. ST. MATTHIAS: Hartert, 1924, Novitates Zool., vol. 31, pp. 261-278. RoOK ISLAND: Rothschild and Hartert, 1914, Novitates Zool., vol. 21, pp. 207- 218. -
Common Birds in Tilligerry Habitat
Common Birds in Tilligerry Habitat Dedicated bird enthusiasts have kindly contributed to this sequence of 106 bird species spotted in the habitat over the last few years Kookaburra Red-browed Finch Black-faced Cuckoo- shrike Magpie-lark Tawny Frogmouth Noisy Miner Spotted Dove [1] Crested Pigeon Australian Raven Olive-backed Oriole Whistling Kite Grey Butcherbird Pied Butcherbird Australian Magpie Noisy Friarbird Galah Long-billed Corella Eastern Rosella Yellow-tailed black Rainbow Lorikeet Scaly-breasted Lorikeet Cockatoo Tawny Frogmouth c Noeline Karlson [1] ( ) Common Birds in Tilligerry Habitat Variegated Fairy- Yellow Faced Superb Fairy-wren White Cheeked Scarlet Honeyeater Blue-faced Honeyeater wren Honeyeater Honeyeater White-throated Brown Gerygone Brown Thornbill Yellow Thornbill Eastern Yellow Robin Silvereye Gerygone White-browed Eastern Spinebill [2] Spotted Pardalote Grey Fantail Little Wattlebird Red Wattlebird Scrubwren Willie Wagtail Eastern Whipbird Welcome Swallow Leaden Flycatcher Golden Whistler Rufous Whistler Eastern Spinebill c Noeline Karlson [2] ( ) Common Sea and shore birds Silver Gull White-necked Heron Little Black Australian White Ibis Masked Lapwing Crested Tern Cormorant Little Pied Cormorant White-bellied Sea-Eagle [3] Pelican White-faced Heron Uncommon Sea and shore birds Caspian Tern Pied Cormorant White-necked Heron Great Egret Little Egret Great Cormorant Striated Heron Intermediate Egret [3] White-bellied Sea-Eagle (c) Noeline Karlson Uncommon Birds in Tilligerry Habitat Grey Goshawk Australian Hobby -
Canberra Bird Notes
canberra ISSN 0314-8211 bird Volume 41 Number 2 June 2016 notes Registered by Australia Post 100001304 CANBERRA ORNITHOLOGISTS GROUP PO Box 301 Civic Square ACT 2608 2014-15 Committee President Alison Russell-French 0419 264 702 Vice-President Neil Hermes 0413 828 045 Secretary Bill Graham 0466 874 723 Treasurer Lia Battisson 6231 0147 (h) Member Jenny Bounds Member Sue Lashko Member Bruce Lindenmayer Member Chris Davey Member Julie McGuiness Member David McDonald Member Paul Fennell Email contacts General enquiries [email protected] President [email protected] Canberra Bird Notes [email protected]/[email protected] COG Database Inquiries [email protected] COG Membership [email protected] COG Web Discussion List [email protected] Conservation [email protected] Gang-gang Newsletter [email protected] GBS Coordinator [email protected] Publications for sale [email protected] Unusual bird reports [email protected] Website [email protected] Woodland Project [email protected] Other COG contacts Jenny Bounds Conservation Field Trips Sue Lashko 6251 4485 (h) COG Membership Sandra Henderson 6231 0303 (h) Canberra Bird Notes Michael Lenz 6249 1109 (h) Newsletter Editor Sue Lashko, Gail Neumann (SL) 6251 4485 (h) Databases Jaron Bailey 0439 270 835 (a. h.) Garden Bird Survey Duncan McCaskill 6259 1843 (h) Rarities Panel Barbara Allan 6254 6520 (h) Talks Program Organiser Jack Holland 6288 7840 (h) Records Officer Nicki Taws 6251 0303 (h) Website Julian Robinson 6239 6226 (h) Sales Kathy Walter 6241 7639 (h) Waterbird Survey Michael Lenz 6249 1109 (h) Distribution of COG publications Dianne Davey 6254 6324 (h) COG Library Barbara Allan 6254 6520 (h) Please use the General Inquiries email to arrange access to library items or for general enquiries, or contact the Secretary on 0466 874 723. -
Disaggregation of Bird Families Listed on Cms Appendix Ii
Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2. -
Fire Management Newsletter: Eucalyptus: a Complex Challenge
Golden Gate National Recreation Area National Park Service U.S. Department of the Interior Point Reyes National Seashore EucalyptusEucalyptus A Complex Challenge AUSTRALIA FIRE MANAGEMENT, RESOURCE PROTECTION, AND THE LEGACY OF TASMANIAN BLUE GUM DURING THE AGE OF EXPLORATION, CURIOUS SPECIES dead, dry, oily leaves and debris—that is especially flammable. from around the world captured the imagination, desire and Carried by long swaying branches, fire spreads quickly in enterprising spirit of many different people. With fragrant oil and eucalyptus groves. When there is sufficient dead material in the massive grandeur, eucalyptus trees were imported in great canopy, fire moves easily through the tree tops. numbers from Australia to the Americas, and California became home to many of them. Adaptations to fire include heat-resistant seed capsules which protect the seed for a critical short period when fire reaches the CALIFORNIA Eucalyptus globulus, or Tasmanian blue gum, was first introduced crowns. One study showed that seeds were protected from lethal to the San Francisco Bay Area in 1853 as an ornamental tree. heat penetration for about 4 minutes when capsules were Soon after, it was widely planted for timber production when exposed to 826o F. Following all types of fire, an accelerated seed domestic lumber sources were being depleted. Eucalyptus shed occurs, even when the crowns are only subjected to intense offered hope to the “Hardwood Famine”, which the Bay Area heat without igniting. By reseeding when the litter is burned off, was keenly aware of, after rebuilding from the 1906 earthquake. blue gum eucalyptus like many other species takes advantage of the freshly uncovered soil that is available after a fire. -
The Avifauna of Mt. Karimui, Chimbu Province, Papua New Guinea, Including Evidence for Long-Term Population Dynamics in Undisturbed Tropical Forest
Ben Freeman & Alexandra M. Class Freeman 30 Bull. B.O.C. 2014 134(1) The avifauna of Mt. Karimui, Chimbu Province, Papua New Guinea, including evidence for long-term population dynamics in undisturbed tropical forest Ben Freeman & Alexandra M. Class Freeman Received 27 July 2013 Summary.—We conducted ornithological feld work on Mt. Karimui and in the surrounding lowlands in 2011–12, a site frst surveyed for birds by J. Diamond in 1965. We report range extensions, elevational records and notes on poorly known species observed during our work. We also present a list with elevational distributions for the 271 species recorded in the Karimui region. Finally, we detail possible changes in species abundance and distribution that have occurred between Diamond’s feld work and our own. Most prominently, we suggest that Bicolored Mouse-warbler Crateroscelis nigrorufa might recently have colonised Mt. Karimui’s north-western ridge, a rare example of distributional change in an avian population inhabiting intact tropical forests. The island of New Guinea harbours a diverse, largely endemic avifauna (Beehler et al. 1986). However, ornithological studies are hampered by difculties of access, safety and cost. Consequently, many of its endemic birds remain poorly known, and feld workers continue to describe new taxa (Prat 2000, Beehler et al. 2007), report large range extensions (Freeman et al. 2013) and elucidate natural history (Dumbacher et al. 1992). Of necessity, avifaunal studies are usually based on short-term feld work. As a result, population dynamics are poorly known and limited to comparisons of diferent surveys or diferences noticeable over short timescales (Diamond 1971, Mack & Wright 1996). -
THE HONEYEATERS of KANGAROO ISLAND HUGH FOB,D Accepted August
134 SOUTH AUsTRALIAN ORNITHOLOGIST, 21 THE HONEYEATERS OF KANGAROO ISLAND HUGH FOB,D Accepted August. 1976 Kangaroo Island is the third largest of Aus In the present paper I discuss morphological tralia's islands (4,500 sq. km) and has been and ecological differences between populations separated from the neighbouring Fleurieu of several species of honeyeaters from Kangaroo Peninsula for 10,000 years (Abbott 1973). A Island and the Fleurieu Peninsula respectively, mere 14 km separates island from mainland; and speculate on how these differences origin but the island has a distinct avifauna and lacks ated. many of the mainland species. This paucity of DIFFERENCES IN PLUMAGE species has been attributed to extinction after The Kangaroo Island population of Purple isolation and failure to recolonise (Abbott gaped Honeyeater was described as larger and 1974, 1976), and to lack of suitable habitat brighter than the mainland population by (Ford and Paton 1975). Mathews (1923-4). Brightness of plumage is a Nine species of honeyeaters are resident on very subjective characteristic, and in my opinion Kangaroo Island. The Purple-gaped Honey Purple-gaped Honeyeaters on Kangaroo Island eater Lichenostomus cratitius (formerly Meli are, if anything, duller than mainland ones. phaga cratitia) was described as a distinct sub Condon (1951) says that the gape of this species by Mathews (1923-24); and Keast species is invariably yellow on Kangaroo Island (1961) mentions that six other species differ in instead of lilac, although he later comments a minor way from mainland populations and that lilac-gaped individuals do occur on the may merit subspecific status. -
Birding Oxley Creek Common Brisbane, Australia
Birding Oxley Creek Common Brisbane, Australia Hugh Possingham and Mat Gilfedder – January 2011 [email protected] www.ecology.uq.edu.au 3379 9388 (h) Other photos, records and comments contributed by: Cathy Gilfedder, Mike Bennett, David Niland, Mark Roberts, Pete Kyne, Conrad Hoskin, Chris Sanderson, Angela Wardell-Johnson, Denis Mollison. This guide provides information about the birds, and how to bird on, Oxley Creek Common. This is a public park (access restricted to the yellow parts of the map, page 6). Over 185 species have been recorded on Oxley Creek Common in the last 83 years, making it one of the best birding spots in Brisbane. This guide is complimented by a full annotated list of the species seen in, or from, the Common. How to get there Oxley Creek Common is in the suburb of Rocklea and is well signposted from Sherwood Road. If approaching from the east (Ipswich Road side), pass the Rocklea Markets and turn left before the bridge crossing Oxley Creek. If approaching from the west (Sherwood side) turn right about 100 m after the bridge over Oxley Creek. The gate is always open. Amenities The main development at Oxley Creek Common is the Red Shed, which is beside the car park (plenty of space). The Red Shed has toilets (composting), water, covered seating, and BBQ facilities. The toilets close about 8pm and open very early. The paths are flat, wide and easy to walk or cycle. When to arrive The diversity of waterbirds is a feature of the Common and these can be good at any time of the day. -
Sericornis, Acanthizidae)
GENETIC AND MORPHOLOGICAL DIFFERENTIATION AND PHYLOGENY IN THE AUSTRALO-PAPUAN SCRUBWRENS (SERICORNIS, ACANTHIZIDAE) LESLIE CHRISTIDIS,1'2 RICHARD $CHODDE,l AND PETER R. BAVERSTOCK 3 •Divisionof Wildlifeand Ecology, CSIRO, P.O. Box84, Lyneham,Australian Capital Territory 2605, Australia, 2Departmentof EvolutionaryBiology, Research School of BiologicalSciences, AustralianNational University, Canberra, Australian Capital Territory 2601, Australia, and 3EvolutionaryBiology Unit, SouthAustralian Museum, North Terrace, Adelaide, South Australia 5000, Australia ASS•CRACr.--Theinterrelationships of 13 of the 14 speciescurrently recognized in the Australo-Papuan oscinine scrubwrens, Sericornis,were assessedby protein electrophoresis, screening44 presumptivelo.ci. Consensus among analysesindicated that Sericorniscomprises two primary lineagesof hithertounassociated species: S. beccarii with S.magnirostris, S.nouhuysi and the S. perspicillatusgroup; and S. papuensisand S. keriwith S. spiloderaand the S. frontalis group. Both lineages are shared by Australia and New Guinea. Patternsof latitudinal and altitudinal allopatry and sequencesof introgressiveintergradation are concordantwith these groupings,but many featuresof external morphologyare not. Apparent homologiesin face, wing and tail markings, used formerly as the principal criteria for grouping species,are particularly at variance and are interpreted either as coinherited ancestraltraits or homo- plasies. Distribution patternssuggest that both primary lineageswere first split vicariantly between -
National Recovery Plan for the Regent Honeyeater (Anthochaera Phrygia)
National Recovery Plan for the Regent Honeyeater (Anthochaera phrygia) April 2016 1 The Species Profile and Threats Database pages linked to this recovery plan is obtainable from: http://www.environment.gov.au/cgi-bin/sprat/public/sprat.pl © Copyright Commonwealth of Australia, 2016. The National Recovery Plan for the Regent Honeyeater (Anthochaera phrygia) is licensed by the Commonwealth of Australia for use under a Creative Commons Attribution 4.0 International licence with the exception of the Coat of Arms of the Commonwealth of Australia, the logo of the agency responsible for publishing the report, content supplied by third parties, and any images depicting people. For licence conditions see: https://creativecommons.org/licenses/by/4.0/. This report should be attributed as ‘National Recovery Plan for the Regent Honeyeater (Anthochaera phrygia), Commonwealth of Australia 2016’. The Commonwealth of Australia has made all reasonable efforts to identify content supplied by third parties using the following format ‘© Copyright, [name of third party] ’. Disclaimer While reasonable efforts have been made to ensure that the contents of this publication are factually correct, the Commonwealth does not accept responsibility for the accuracy or completeness of the contents, and shall not be liable for any loss or damage that may be occasioned directly or indirectly through the use of, or reliance on, the contents of this publication. Image credits Front Cover: Regent honeyeaters in the Capertee Valley, NSW. (© Copyright, Dean Ingwersen). 2 -
Papua New Guinea IV Trip Report 22Nd July to 8Th August 2018 (18 Days)
Papua New Guinea IV Trip Report 22nd July to 8th August 2018 (18 days) Flame Bowerbird by Glen Valentine Tour Leaders: Glen Valentine & David Erterius Trip report compiled by Glen Valentine Trip Report – RBL Papua New Guinea IV 2018 2 Top 10 birds of the tour as voted for by the tour participants: 1. Flame Bowerbird 2. King-of-Saxony Bird-of-Paradise 3. Wattled Ploughbill 4. Blue-capped Ifrit, King Bird-of-Paradise & Papuan Frogmouth 5. Wallace’s Fairywren, Superb Bird-of-Paradise, Wallace’s Owlet-nightjar, MacGregor’s Bowerbird (for its elaborate bower!) & Brown Sicklebill, 6. Queen Carola’s Parotia 7. Brown-headed Paradise Kingfisher 8. Moustached Treeswift, Blue Jewel-babbler, Emperor Fairywren & Orange-fronted Hanging Parrot 9. Crested Berrypecker & Black-capped Lory 10. Red-breasted Pygmy Parrot Sclater’s Crowned Pigeon by Glen Valentine Tour Summary Tucked away between the Lesser Sundas and the expansive continent of Australia is the legendary island of New Guinea. Home to the spectacular birds-of-paradise, arguably the world’s most attractive and intriguing bird family, New Guinea will always be one of those very special destinations that every birder wishes to visit sometime in their lives. Rockjumper Birding Tours Trip Report – RBL Papua New Guinea IV 2018 3 Our fourth of six comprehensive birding tours to Papua New Guinea (the eastern half of the island of New Guinea) for the 2018 season coincided, as always with the dry season and the advent of displaying birds-of-paradise. The trip was a resounding success once again and racked -
Bush Birds Making Your Place Their Place Too
BUSH BIRDS MAKING YOUR PLACE THEIR PLACE TOO This fact sheet explains which bush birds may be present or absent from your place and what you can do to encourage a greater diversity to live with you. The drier, settled areas of southern Tasmania, and whistlers. Some, like Pink Robin and Scrubtit, compared to other places, still have much of their prefer wet forest and others, such as Forty- original bush. In many instances the clearing for spotted Pardalote are rarely seen outside their agriculture and urban development has produced preferred specialist habitat. a mosaic of habitats including highly modified The Yellow-throated Honeyeater needs bush with Some species live in the same bush all year, treeless paddocks through to fully vegetated hills, good structure, as it forages high in trees but nests whilst others migrate in the late autumn to in which many species of birds still thrive. But bird in shrubs close to the ground. increase their foraging range, descend in species begin to decline or will be absent where altitude or cross Bass Strait to spend their intact patches of bush are lost or if this mosaic winter on mainland Australia. Bush habitat also BUSH BIRDS’ HOMES becomes too highly modified. supports birds of prey, water birds in creeks and Just like us, birds have three basic needs: About 60 species of birds live within the bush of wetlands, and a small number of other species 1. Their preferred food. southern Tasmania. Common groups of species using heaths or grasslands on the forest fringe. include honeyeaters, parrots, robins, pardalotes 2.