Restoring Paradise Predator Free Lord Howe Island
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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. -
Iucn Red Data List Information on Species Listed On, and Covered by Cms Appendices
UNEP/CMS/ScC-SC4/Doc.8/Rev.1/Annex 1 ANNEX 1 IUCN RED DATA LIST INFORMATION ON SPECIES LISTED ON, AND COVERED BY CMS APPENDICES Content General Information ................................................................................................................................................................................................................................ 2 Species in Appendix I ............................................................................................................................................................................................................................... 3 Mammalia ............................................................................................................................................................................................................................................ 4 Aves ...................................................................................................................................................................................................................................................... 7 Reptilia ............................................................................................................................................................................................................................................... 12 Pisces ................................................................................................................................................................................................................................................. -
Noio Or Black Noddy Anous Minutus
Seabirds Noio or Black Noddy Anous minutus SPECIES STATUS: State recognized as Indigenous NatureServe Heritage Rank G5 - Secure North American Waterbird Conservation Plan – Photo: USFWS Moderate concern Regional Seabird Conservation Plan - USFWS 2005 SPECIES INFORMATION: The noio or black noddy is a medium-sized, abundant, and gregarious tern (Family: Laridae) with a pantropical distribution. Seven noio (black noddy) subspecies are generally recognized, and two are resident in Hawai‘i: A. s. melanogenys (MHI) and A. s. marcusi (NWHI). Individuals have slender wings, a wedge-shaped tail, and black bill which is slightly decurved. Adult males and females are sooty black with a white cap and have reddish brown legs and feet; bill droops slightly. Flight is swift with rapid wing beats and usually direct and low over the ocean; this species almost never soars high. Often forages in large, mixed species flocks associated with schools of large predatory fishes which drive prey species to the surface. Noio (black noddy) generally forage in nearshore waters and feeds mainly by dipping the surface from the wing or by making shallow dives. Opportunistic, in Hawai‘i, noio (black noddy) primarily takes juvenile goatfish, lizardfish, herring, flyingfish, and gobies. Nests in large, dense colonies that include non-breeding juvenile birds. Established pairs return to the same nest site year after year. Breeding is highly variable and egg laying occurs year-round. Both parents incubate single egg, and brood and feed chick. Birds first breed at two to three years of age, and the oldest known individual was 25 years old. DISTRIBUTION: Noio (black noddy) breed throughout the Hawaiian Archipelago, including all islands of NWHI and the coastal cliffs and offshore islets of MHI. -
Proposal for Inclusion of the Black Noddy Subspecies Worcesteri
CMS Distribution: General CONVENTION ON MIGRATORY UNEP/CMS/COP12/Doc.25.1.12 15 June 2017 SPECIES Original: English 12th MEETING OF THE CONFERENCE OF THE PARTIES Manila, Philippines, 23 - 28 October 2017 Agenda Item 25.1 PROPOSAL FOR THE INCLUSION OF THE BLACK NODDY (Anous minutus) SUBSPECIES worcesteri ON APPENDIX II OF THE CONVENTION Summary: The Government of the Philippines has submitted the attached proposal* for the inclusion of the Black Noddy (Anous minutus) subspecies worcesteri on Appendix II of CMS. *The geographical designations employed in this document do not imply the expression of any opinion whatsoever on the part of the CMS Secretariat (or the United Nations Environment Programme) concerning the legal status of any country, territory, or area, or concerning the delimitation of its frontiers or boundaries. The responsibility for the contents of the document rests exclusively with its author. UNEP/CMS/COP12/Doc.25.1.12 PROPOSAL FOR THE INCLUSION OF THE BLACK NODDY (Anous minutus) SUBSPECIES worcesteri ON APPENDIX II OF THE CONVENTION ON THE CONSERVATION OF MIGRATORY SPECIES OFWILD ANIMALS A. PROPOSAL This proposal is for the inclusion of Black Noddy (Anous minutus) subspecies worcesteri in Appendix II. The species is classified as Endangered on account of a very small population which breeds within a tiny area of occupancy on just two islets, and is projected to decline by more than 70 per cent over the next 10 to 15 years. B. PROPONENT: Government of the Republic of the Philippines C. SUPPORTING STATEMENT 1. Taxonomy 1.1 Class: Aves 1.2 Order: Charadriiformes 1.3 Family: Laridae 1.4 Genus, species or subspecies, including author and year: Anous minutus worcesteri (McGregor, 1911) 1.5 Scientific synonyms: No known synonyms 1.6 Common name(s), in all applicable languages used by the Convention: English - Black Noddy French - Noddi noir Spanish - Tiñosa menuda 2. -
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. -
Observations of Pelagic Seabirds Wintering at Sea in the Southeastern Caribbean William L
Pp. 104-110 in Studies in Trinidad and Tobago Ornithology Honouring Richard ffrench (F. E. Hayes and S. A. Temple, Eds.). Dept. Life Sci., Univ. West Indies, St. Augustine, Occ. Pap. 11, 2000 OBSERVATIONS OF PELAGIC SEABIRDS WINTERING AT SEA IN THE SOUTHEASTERN CARIBBEAN WILLIAM L. MURPHY, 8265 Glengarry Court, Indianapolis, IN 46236, USA ABSTRACT.-I report observations, including several the educational cruise ship Yorktown Clipper between significant distributional records, of 16 species of Curaçao and the Orinoco River, traversing seabirds wintering at sea in the southeastern Caribbean approximately 2,000 km per trip (Table 1). Because during cruises from Bonaire to the Orinoco River (5-13 the focus was on visiting islands as well as on cruising, January 1996, 3-12 March 1997, and 23 December many of the longer passages were traversed at night. 1997 - 1 January 1998). A few scattered shearwaters While at sea during the day, fellow birders and I (Calonectris diomedea and Puffinus lherminieri) were maintained a sea watch, recording sightings of bird seen. Storm-Petrels (Oceanites oceanicus and species and their numbers. Oceanodroma leucorhoa), particularly the latter species, were often seen toward the east. Most The observers were all experienced birders with tropicbirds (Phaethon aethereus) and gulls (Larus binoculars, some of which were image-stabilised. The atricilla) were near Tobago. Boobies were common; number of observers at any given time ranged from Sula leucogaster outnumbered S. sula by about 4:1 and one to 15, averaging about five. Observations were S. dactylatra was scarce. Frigatebirds (Fregata made from various points on three decks ranging from magnificens) were strictly coastal. -
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.