Nocturnal at Norfolk Island? DAVID G
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Australian Diurnal Raptors and Airports
Australian diurnal raptors and airports Photo: John Barkla, BirdLife Australia William Steele Australasian Raptor Association BirdLife Australia Australian Aviation Wildlife Hazard Group Forum Brisbane, 25 July 2013 So what is a raptor? Small to very large birds of prey. Diurnal, predatory or scavenging birds. Sharp, hooked bills and large powerful feet with talons. Order Falconiformes: 27 species on Australian list. Family Falconidae – falcons/ kestrels Family Accipitridae – eagles, hawks, kites, osprey Falcons and kestrels Brown Falcon Black Falcon Grey Falcon Nankeen Kestrel Australian Hobby Peregrine Falcon Falcons and Kestrels – conservation status Common Name EPBC Qld WA SA FFG Vic NSW Tas NT Nankeen Kestrel Brown Falcon Australian Hobby Grey Falcon NT RA Listed CR VUL VUL Black Falcon EN Peregrine Falcon RA Hawks and eagles ‐ Osprey Osprey Hawks and eagles – Endemic hawks Red Goshawk female Hawks and eagles – Sparrowhawks/ goshawks Brown Goshawk Photo: Rik Brown Hawks and eagles – Elanus kites Black‐shouldered Kite Letter‐winged Kite ~ 300 g Hover hunters Rodent specialists LWK can be crepuscular Hawks and eagles ‐ eagles Photo: Herald Sun. Hawks and eagles ‐ eagles Large ‐ • Wedge‐tailed Eagle (~ 4 kg) • Little Eagle (< 1 kg) • White‐bellied Sea‐Eagle (< 4 kg) • Gurney’s Eagle Scavengers of carrion, in addition to hunters Fortunately, mostly solitary although some multiple strikes on aircraft Hawks and eagles –large kites Black Kite Whistling Kite Brahminy Kite Frequently scavenge Large at ~ 600 to 800 g BK and WK flock and so high risk to aircraft Photo: Jill Holdsworth Identification Beruldsen, G (1995) Raptor Identification. Privately published by author, Kenmore Hills, Queensland, pp. 18‐19, 26‐27, 36‐37. -
Observations on the Raptor Community of the Pilbara Region of Western Australia
129 AUSTRALIAN FIELD ORNITHOLOGY 2011, 28, 129–132 Observations on the Raptor Community of the Pilbara Region of Western Australia A.J.G. SUTTON 157 Nawaday Way, Singleton, New South Wales 2330 (Email: [email protected]) Summary Fourteen species of diurnal raptor were observed during roadside surveys and nest searches of the Newman district, in the eastern Pilbara region of arid north-western Australia, in 1987–88. Breeding data (months in which nestlings were present) are presented for eight of these species, and dietary observations or pellet analyses are presented for five. Raptor community structure, particularly with respect to bird-eating falcons in various size-classes, appeared similar to that elsewhere in the arid zone. Introduction There has been only one detailed study of the diurnal raptor community in the Australian arid zone, in the south-west of the Northern Territory (Aumann 2001a–d). Otherwise, apart from historical annotated bird or raptor lists for parts of the arid zone, there has been one other study of diurnal raptors, in arid north- eastern South Australia (Falkenberg et al. 2000; Falkenberg 2011), and an anecdotal account of some of the raptors at sites also in arid South Australia (Debus et al. 2006). This paper presents the results of road-transect surveys and nest searches for raptors in arid north-western Australia, obtained during a study on the Grey Falcon Falco hypoleucos (see Sutton 2011). Study area and methods The study area was that part of the Pilbara region within a 100-km radius of Newman (23°21′S, 119°43′E), in the Ophthalmia Range off the eastern Hamersley Range in arid north-western Western Australia (see Sutton 2011 for further details and references). -
History and Causes of the Extirpation of the Providence Petrel (Pterodroma Solandri) on Norfolk Island
246 Notornis, 2002, Vol. 49: 246-258 0029-4470 O The Ornithological Society of New Zealand, Inc. 2002 History and causes of the extirpation of the Providence petrel (Pterodroma solandri) on Norfolk Island DAVID G. MEDWAY 25A Norman Street, New Plymouth, New Zealand [email protected] Abstract The population of Providence petrels (Pterodroma solandri) that nested on Norfolk Island at the time of 1st European settlement of that island in 1788 was probably > 1 million pairs. Available evidence indicates that Europeans harvested many more Providence petrels in the years immediately after settlement than previously believed. About 1,000,000 Providence petrels, adults and young, were harvested in the 4 breeding seasons from 1790 to 1793 alone. Despite these enormous losses, many Providence petrels were apparently still nesting on Norfolk Island in 1795 when they are last mentioned in documents from the island. However, any breeding population that may have survived there until 1814 when Norfolk Island was abandoned temporarily was probably exterminated by the combined activities of introduced cats and pigs which had become very numerous by the time the island was re-occupied in 1825. Medway, D.G. 2002. History and causes of the exhrpation of the Providence petrel (Pterodroma solandri) on Norfolk Island. Notornis 49(4): 246-258. Keywords Norfolk Island; Providence petrel; Pterodroma solandri; human harvesting; mammalian predation; extupation INTRODUCTION in to a hole which was concealed by the birds Norfolk Island (29" 02'S, 167" 57'E; 3455 ha), an making their burrows slant-wise". From the Australian external territory, is a sub-tropical summit, King had a view of the whole island and island in the south-west Pacific. -
A Guide to the Birds of Barrow Island
A Guide to the Birds of Barrow Island Operated by Chevron Australia This document has been printed by a Sustainable Green Printer on stock that is certified carbon in joint venture with neutral and is Forestry Stewardship Council (FSC) mix certified, ensuring fibres are sourced from certified and well managed forests. The stock 55% recycled (30% pre consumer, 25% post- Cert no. L2/0011.2010 consumer) and has an ISO 14001 Environmental Certification. ISBN 978-0-9871120-1-9 Gorgon Project Osaka Gas | Tokyo Gas | Chubu Electric Power Chevron’s Policy on Working in Sensitive Areas Protecting the safety and health of people and the environment is a Chevron core value. About the Authors Therefore, we: • Strive to design our facilities and conduct our operations to avoid adverse impacts to human health and to operate in an environmentally sound, reliable and Dr Dorian Moro efficient manner. • Conduct our operations responsibly in all areas, including environments with sensitive Dorian Moro works for Chevron Australia as the Terrestrial Ecologist biological characteristics. in the Australasia Strategic Business Unit. His Bachelor of Science Chevron strives to avoid or reduce significant risks and impacts our projects and (Hons) studies at La Trobe University (Victoria), focused on small operations may pose to sensitive species, habitats and ecosystems. This means that we: mammal communities in coastal areas of Victoria. His PhD (University • Integrate biodiversity into our business decision-making and management through our of Western Australia) -
A Plague of Mice at Warren by J
July J HOBBS, Mice Plague 43 r971 who made the first general ornithological collection in the area. That man, a young fellow named George Harper, who had reached Australia from Britain about 1820 with letters of recom mendation from Sir Walter Scott, was given a grant of land at Picton, whence he appears to have ranged considerably in amas sing natural history material. In consequence, according to the Sydney Gazette of February 3, 1827, he was then able to take to Britain a great many specimens, including no fewer than 1675 bird skins, as well as two living Emus that rather alarmed Sir Walter Scott. Some of Harper's bird-skins were bought by Sir William Jardine; others were acquired by the Edinburgh Museum. It would be interesting now, 140-odd years later, to have news of those specimens. A Plague of Mice at Warren By J. N. HOBBS, Katoomba, New South Wales INTRODUCTION It is generally accepted that certain species of birds will con gregate at plagues of insects or rodents, but more detailed docu mentations of such visitations are rare. House Mice, Mus musculus were in plague proportions in many parts of the wheat belt of eastern and southern Australia in the autumn and early winter of 1970. In May 1970, I made a short visit to Warren, New South Wales, one of the areas overrun by the mice. I had been there also in December 1969, before the build-up in the numbers of mice, and, therefore, was able to mal<e a comparison of the numbers of known and probable birct"'predators of mice at the two visits. -
Marine Aquaculture Research Lease Providence Bay, Port Stephens NSW Environmental Impact Statement
Marine Aquaculture Research Lease Providence Bay, Port Stephens NSW Environmental Impact Statement Prepared By: Hester Bushell BSc (Marine Science and Management) and Aquaculture Management Unit (NSW Department of Primary Industries) Prepared For: NSW Department of Primary Industries Port Stephens Fisheries Institute Taylors Beach Road, Taylors Beach NSW 2316 October 2012 Cover Image: Yellowtail Kingfish in a research tank at PSFI (Source: NSW DPI, 2008). © State of New South Wales through Department of Trade and Investment, Regional Infrastructure and Services 2012. This publication is copyright. You may download, display, print and reproduce this material in an unaltered form only (retaining this notice) for your personal use or for non-commercial use within your organisation. To copy, adapt, publish, distribute or commercialise any of this publication you will need to seek permission from the Department of Trade and Investment, Regional Infrastructure and Services. For updates to this publication, check www.dpi.nsw.gov.au/fisheries. Published by the NSW Department of Primary Industries, a part of the Department of Trade and Investment, Regional Infrastructure and Services. First published October 2012 ISBN: 978 1 74256 365 7 DISCLAIMER The information contained in this publication is based on knowledge and understanding at the time of writing (September 2012). However, because of advances in knowledge, users are reminded of the need to ensure that information on which they rely is up to date and to check the currency of the information -
AOU Classification Committee – North and Middle America
AOU Classification Committee – North and Middle America Proposal Set 2015-A 21 Jan 2015 No. Page Title 01 02 Revise the classification of the Pipridae 02 08 Add Bicolored Wren Campylorhynchus griseus to the Main List 03 11 Move Dusky Pigeon Patagioenas goodsoni from the Appendix to the Main List 04 14 Revise the classification of the Psittaciformes 05 19 Split Pterodroma heraldica and P. atrata from Herald Petrel P. arminjoniana 06 26 Transfer American Tree Sparrow Spizella arborea to Spizelloides 07 28 Split Passerina pallidior from Painted Bunting P. ciris 08 32 Split Toxostoma arenicola from LeConte’s Thrasher T. lecontei 09 35 Correct the scientific names of (a) Leptotila cassini and (b) Amazilia saucerrottei 10 37 Split Laysan Honeycreeper from Apapane Himatione sanguinea and change its specific epithet to fraithii 11 40 Split Newell’s Shearwater Puffinus newelli from Townsend’s Shearwater P. auricularis, and consider Rapa Shearwater P. myrtae as a species separate from P. newelli 12 44 Correct the citation for Pterodroma solandri 2015-A-1 N&MA Classification Committee pp. 423-426 Revise the classification of the Pipridae Background: Our current classification of the Pipridae is as follows: Corapipo altera Chiroxiphia lanceolata Chiroxiphia linearis Xenopipo holochlora Dixiphia pipra Ceratopipra mentalis Ceratopipra erythrocephala Manacus candei Manacus aurantiacus Manacus vitellinus Lepidothrix coronata New information: Ohlson et al. (2013) investigated relationships within the family using DNA sequence data from three nuclear introns and one mitochondrial gene (ND2). They sampled all genera and most species. I have pasted in a screen grab of their tree below. Their results are largely consistent with those of previous studies except for the polyphyly of Chloropipo, members of which are in three parts of the tree. -
Conservation Status of New Zealand Birds, 2008
Notornis, 2008, Vol. 55: 117-135 117 0029-4470 © The Ornithological Society of New Zealand, Inc. Conservation status of New Zealand birds, 2008 Colin M. Miskelly* Wellington Conservancy, Department of Conservation, P.O. Box 5086, Wellington 6145, New Zealand [email protected] JOHN E. DOWDING DM Consultants, P.O. Box 36274, Merivale, Christchurch 8146, New Zealand GRAEME P. ELLIOTT Research & Development Group, Department of Conservation, Private Bag 5, Nelson 7042, New Zealand RODNEY A. HITCHMOUGH RALPH G. POWLESLAND HUGH A. ROBERTSON Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand PAUL M. SAGAR National Institute of Water & Atmospheric Research, P.O. Box 8602, Christchurch 8440, New Zealand R. PAUL SCOFIELD Canterbury Museum, Rolleston Ave, Christchurch 8001, New Zealand GRAEME A. TAYLOR Research & Development Group, Department of Conservation, P.O. Box 10420, Wellington 6143, New Zealand Abstract An appraisal of the conservation status of the post-1800 New Zealand avifauna is presented. The list comprises 428 taxa in the following categories: ‘Extinct’ 20, ‘Threatened’ 77 (comprising 24 ‘Nationally Critical’, 15 ‘Nationally Endangered’, 38 ‘Nationally Vulnerable’), ‘At Risk’ 93 (comprising 18 ‘Declining’, 10 ‘Recovering’, 17 ‘Relict’, 48 ‘Naturally Uncommon’), ‘Not Threatened’ (native and resident) 36, ‘Coloniser’ 8, ‘Migrant’ 27, ‘Vagrant’ 130, and ‘Introduced and Naturalised’ 36. One species was assessed as ‘Data Deficient’. The list uses the New Zealand Threat Classification System, which provides greater resolution of naturally uncommon taxa typical of insular environments than the IUCN threat ranking system. New Zealand taxa are here ranked at subspecies level, and in some cases population level, when populations are judged to be potentially taxonomically distinct on the basis of genetic data or morphological observations. -
Avifauna from the Emily Bay Settlement Site, Norfolk Island: a Preliminary Account
© Copyright Australian Museum, 2001 Records of the Australian Museum, Supplement 27 (2001): 85–100. ISBN 0 7347 2305 9 Avifauna from the Emily Bay Settlement Site, Norfolk Island: A Preliminary Account RICHARD N. HOLDAWAY1 AND ATHOLL ANDERSON2 1 Palaecol Research, PO Box 16569, Christchurch, New Zealand [email protected] 2 Department of Archaeology & Natural History, Research School of Pacific and Asian Studies, Australian National University, Canberra ACT 0200, Australia [email protected] ABSTRACT. The avifauna of the Emily Bay settlement site, Norfolk Island, southwest Pacific, is described. Most of the remains, which consisted of nearly 10,000 identifiable bones (mostly fragmentary) and several thousand unidentifiable elements and fragments, were of several species of petrel and shearwater (Procellariiformes) and boobies (Sulidae), but some land birds were also represented in small numbers. Two species of migratory wading bird (Charadriiformes) were identified in the deposits, but no terns, which are dominant members of the present avifauna. The taphonomy of the remains indicates intensive use of birds as food, but some material of other than cultural origin was also present. Remains were not distributed evenly throughout the excavated parts of the site, and were concentrated in areas where other evidence such as post holes and fires scoops indicated points of occupation. Some species that are present on the island and palatable were not represented in the collections: possible reasons for their absence are canvassed. An estimate of the biomass is presented, with the proviso that the variation in density of deposition made extrapolation to the remainder of the site problematic. The size of the sample, the preservation of elements such as vertebrae of small petrels, and the good condition of material of apparent natural (non-cultural) origin indicate that the collection represents a good sample of the avifauna used as food by the Polynesian inhabitants of Emily Bay. -
Investigating Spatiotemporal Variation in the Diet of Westland Petrel Through
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.30.360289; this version posted August 17, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Investigating spatiotemporal variation in the diet of Westland Petrel through 2 metabarcoding, a non-invasive technique 3 Marina Querejeta1, Marie-Caroline Lefort2,3, Vincent Bretagnolle4, Stéphane Boyer1,2 4 5 6 1 Institut de Recherche sur la Biologie de l'Insecte, UMR 7261, CNRS-Université de Tours, 7 Tours, France 8 2 Environmental and Animal Sciences, Unitec Institute of Technology, 139 Carrington Road, 9 Mt Albert, Auckland 1025, New Zealand 10 3 Cellule de Valorisation Pédagogique, Université de Tours, 60 rue du Plat d’Étain, 37000 11 Tours, France. 12 4 Centre d’Études Biologiques de Chizé, UMR 7372, CNRS & La Rochelle Université, 79360 13 Villiers en Bois, France. 14 15 16 17 18 19 Running head: Spatiotemporal variation in diet of Westland Petrel 20 21 Keywords: Conservation, metabarcoding, dietary DNA, biodiversity, New Zealand, 22 Procellaria westlandica 23 24 Abstract 25 As top predators, seabirds are in one way or another impacted by any changes in marine 26 communities, whether they are linked to climate change or caused by commercial fishing 27 activities. However, their high mobility and foraging behaviour enables them to exploit prey 28 distributed patchily in time and space. This capacity of adaptation comes to light through 29 the study of their diet. -
Status and Occurrence of Murphy's Petrel (Pterodroma Ultima) in British Columbia. by Rick Toochin and Louis Haviland. Submitte
Status and Occurrence of Murphy’s Petrel (Pterodroma ultima) in British Columbia. By Rick Toochin and Louis Haviland. Submitted: April 15, 2018. Introduction and Distribution The Murphy’s Petrel (Pterodroma ultima) is a seldom seen seabird species that is listed by Bird Life International (2016) and IUCN (2016) as Near Threatened. This species breeds on islands of the Tropical Pacific Ocean from the Pitcairn Island group (Henderson Island, Oeno Island, and Ducie Island) (Murphy and Pennoyer 1952); the Tuamotu Island group (Mururoa Island and Fangataufa Island); islets of Rapa (Austral group) (Garnett 1984); and Manui in Gambier group (Thibault 1988); Easter Island and Salas y Gomez, Chile (Flores et al. 2014); and possibly on Cook Island (Gill 1996); and the Juan Fernandez Islands (Flood et al. 2016). In the Pitcairn Islands, an estimated 2,500 (± 500) bred on Henderson, 12,500 (± 2,500) on Oeno, and 250,000 (± 29,000) on Ducie (Brooke 1995). Following rat eradication on Oeno in 1997, the population there had grown to at least 25,000 pairs in 2013 (IUCN 2016) In the Tuamotu Islands, colonies occur on Mururoa and Fangataufa (Holyoak and Thibault 1984), although these may have disappeared owing to nuclear tests and the recent construction of an airstrip (IUCN 2016). In the Austral Islands, it breeds only on a limited number of islets off Rapa where the population was estimated at 10-100 pairs in 1990 (Thibault and Varney 1991). In the Gambier Islands, proof of breeding was found for the first time on Manui and numbers were estimated at 5-10 pairs (Thibault and Bretagnolle 1999). -
Threats to Seabirds: a Global Assessment 2 3 4 Authors: Maria P
1 Threats to seabirds: a global assessment 2 3 4 Authors: Maria P. Dias1*, Rob Martin1, Elizabeth J. Pearmain1, Ian J. Burfield1, Cleo Small2, Richard A. 5 Phillips3, Oliver Yates4, Ben Lascelles1, Pablo Garcia Borboroglu5, John P. Croxall1 6 7 8 Affiliations: 9 1 - BirdLife International. The David Attenborough Building, Pembroke Street Cambridge CB2 3QZ UK 10 2 - BirdLife International Marine Programme, RSPB, The Lodge, Sandy, SG19 2DL 11 3 – British Antarctic Survey. Natural Environment Research Council, High Cross, Madingley Road, 12 Cambridge CB3 0ET, UK 13 4 – Centre for the Environment, Fishery and Aquaculture Science, Pakefield Road, Lowestoft, NR33, UK 14 5 - Global Penguin Society, University of Washington and CONICET Argentina. Puerto Madryn U9120, 15 Chubut, Argentina 16 * Corresponding author: Maria Dias, [email protected]. BirdLife International. The David 17 Attenborough Building, Pembroke Street Cambridge CB2 3QZ UK. Phone: +44 (0)1223 747540 18 19 20 Acknowledgements 21 We are very grateful to Bartek Arendarczyk, Sophie Bennett, Ricky Hibble, Eleanor Miller and Amy 22 Palmer-Newton for assisting with the bibliographic review. We thank Rachael Alderman, Pep Arcos, 23 Jonathon Barrington, Igor Debski, Peter Hodum, Gustavo Jimenez, Jeff Mangel, Ken Morgan, Paul Sagar, 24 Peter Ryan, and other members of the ACAP PaCSWG, and the members of IUCN SSC Penguin Specialist 25 Group (Alejandro Simeone, Andre Chiaradia, Barbara Wienecke, Charles-André Bost, Lauren Waller, Phil 26 Trathan, Philip Seddon, Susie Ellis, Tom Schneider and Dee Boersma) for reviewing threats to selected 27 species. We thank also Andy Symes, Rocio Moreno, Stuart Butchart, Paul Donald, Rory Crawford, 28 Tammy Davies, Ana Carneiro and Tris Allinson for fruitful discussions and helpful comments on earlier 29 versions of the manuscript.