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Biology and Conservation of the Juan Fernandez Archipelago Seabird Community
Biology and Conservation of the Juan Fernández Archipelago Seabird Community Peter Hodum and Michelle Wainstein Dates: 29 December 2001 – 29 March 2002 Participants: Dr. Peter Hodum California State University at Long Beach Long Beach, CA USA Dr. Michelle Wainstein University of Washington Seattle, WA USA Erin Hagen University of Washington Seattle, WA USA Additional contributors: 29 December 2001 – 19 January 2002 Brad Keitt Island Conservation Santa Cruz, CA USA Josh Donlan Island Conservation Santa Cruz, CA USA Karl Campbell Charles Darwin Foundation Galapagos Islands Ecuador 14 January 2002 – 24 March 2002 Ronnie Reyes (student of Dr. Roberto Schlatter) Universidad Austral de Chile Valdivia Chile TABLE OF CONTENTS Introduction 3 Objectives 3 Research on the pink-footed shearwater 3 Breeding population estimates 4 Reproductive biology and behavior 6 Foraging ecology 7 Competition and predation 8 The storm 9 Research on the Juan Fernández and Stejneger’s petrels 10 Population biology 10 Breeding biology and behavior 11 Foraging ecology 14 Predation 15 The storm 15 Research on the Kermadec petrel 16 Community Involvement 17 Public lectures 17 Seabird drawing contest 17 Radio show 18 Material for CONAF Information Center 18 Local pink-footed shearwater reserve 18 Conservation concerns 19 Streetlights 19 Eradication and restoration 19 Other fauna 20 Acknowledgements 20 Figure 1. Satellite tracks for pink-footed shearwaters 22 Appendices (for English translations please contact P. Hodum or M. Wainstein) A. Proposal for Kermadec petrel research 23 B. Natural history materials left with Information Center 24 C. Proposal for a local shearwater reserve 26 D. Contact information 32 2 INTRODUCTION Six species of seabirds breed on the Juan Fernández Archipelago: the pink-footed shearwater (Puffinus creatopus), Juan Fernández petrel (Pterodroma externa), Stejneger’s petrel (Pterodroma longirostris), Kermadec petrel (Pterodroma neglecta), white-bellied storm petrel (Fregetta grallaria), and Defilippe’s petrel (Pterodroma defilippiana). -
Seabirds in Southeastern Hawaiian Waters
WESTERN BIRDS Volume 30, Number 1, 1999 SEABIRDS IN SOUTHEASTERN HAWAIIAN WATERS LARRY B. SPEAR and DAVID G. AINLEY, H. T. Harvey & Associates,P.O. Box 1180, Alviso, California 95002 PETER PYLE, Point Reyes Bird Observatory,4990 Shoreline Highway, Stinson Beach, California 94970 Waters within 200 nautical miles (370 km) of North America and the Hawaiian Archipelago(the exclusiveeconomic zone) are consideredas withinNorth Americanboundaries by birdrecords committees (e.g., Erickson and Terrill 1996). Seabirdswithin 370 km of the southern Hawaiian Islands (hereafterreferred to as Hawaiian waters)were studiedintensively by the PacificOcean BiologicalSurvey Program (POBSP) during 15 monthsin 1964 and 1965 (King 1970). Theseresearchers replicated a tracklineeach month and providedconsiderable information on the seasonaloccurrence and distributionof seabirds in these waters. The data were primarily qualitative,however, because the POBSP surveyswere not basedon a strip of defined width nor were raw counts corrected for bird movement relative to that of the ship(see Analyses). As a result,estimation of density(birds per unit area) was not possible. From 1984 to 1991, using a more rigoroussurvey protocol, we re- surveyedseabirds in the southeasternpart of the region (Figure1). In this paper we providenew informationon the occurrence,distribution, effect of oceanographicfactors, and behaviorof seabirdsin southeasternHawai- ian waters, includingdensity estimatesof abundant species. We also document the occurrenceof six speciesunrecorded or unconfirmed in thesewaters, the ParasiticJaeger (Stercorarius parasiticus), South Polar Skua (Catharacta maccormicki), Tahiti Petrel (Pterodroma rostrata), Herald Petrel (P. heraldica), Stejneger's Petrel (P. Iongirostris), and Pycroft'sPetrel (P. pycrofti). STUDY AREA AND SURVEY PROTOCOL Our studywas a piggybackproject conducted aboard vessels studying the physicaloceanography of the easterntropical Pacific. -
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. -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma -
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 ................................................................................................................................................................................................................................................. -
Habitat Types
Habitat Types The following section features ten predominant habitat types on the West Coast of the Eyre Peninsula, South Australia. It provides a description of each habitat type and the native plant and fauna species that commonly occur there. The fauna species lists in this section are not limited to the species included in this publication and include other coastal fauna species. Fauna species included in this publication are printed in bold. Information is also provided on specific threats and reference sites for each habitat type. The habitat types presented are generally either characteristic of high-energy exposed coastline or low-energy sheltered coastline. Open sandy beaches, non-vegetated dunefields, coastal cliffs and cliff tops are all typically found along high energy, exposed coastline, while mangroves, sand flats and saltmarsh/samphire are characteristic of low energy, sheltered coastline. Habitat Types Coastal Dune Shrublands NATURAL DISTRIBUTION shrublands of larger vegetation occur on more stable dunes and Found throughout the coastal environment, from low beachfront cliff-top dunes with deep stable sand. Most large dune shrublands locations to elevated clifftops, wherever sand can accumulate. will be composed of a mosaic of transitional vegetation patches ranging from bare sand to dense shrub cover. DESCRIPTION This habitat type is associated with sandy coastal dunes occurring The understory generally consists of moderate to high diversity of along exposed and sometimes more sheltered coastline. Dunes are low shrubs, sedges and groundcovers. Understory diversity is often created by the deposition of dry sand particles from the beach by driven by the position and aspect of the dune slope. -
Breeding Biology of the Brown Noddy on Tern Island, Hawaii
Wilson Bull., 108(2), 1996, pp. 317-334 BREEDING BIOLOGY OF THE BROWN NODDY ON TERN ISLAND, HAWAII JENNIFER L. MEGYESI’ AND CURTICE R. GRIFFINS ABSTRACT.-we observed Brown Noddy (Anous stolidus pileatus) breeding phenology and population trends on Tern Island, French Frigate Shoals, Hawaii, from 1982 to 1992. Peaks of laying ranged from the first week in January to the first week in November; however, most laying occurred between March and September each year. Incubation length was 34.8 days (N = 19, SD = 0.6, range = 29-37 days). There were no differences in breeding pairs between the measurements of the first egg laid and successive eggs laid within a season. The proportion of light- and dark-colored chicks was 26% and 74%, respectively (N = 221) and differed from other Brown Noddy colonies studied in Atlantic and Pacific oceans. The length of time between clutches depended on whether the previous outcome was a failed clutch or a successfully fledged chick. Hatching, fledging, and reproductive success were significantly different between years. The subspecies (A. s. pihtus) differs in many aspects of its breeding biology from other colonies in the Atlantic and Pacific oceans, in regard to year-round occurrence at the colony, frequent renesting attempts, large egg size, proportion of light and dark colored chicks, and low reproductive success caused by in- clement weather and predation by Great Frigatebirds (Fregata minor). Received 31 Mar., 1995, accepted 5 Dec. 1995. The Brown Noddy (Anous stolidus) is the largest and most widely distributed of the tropical and subtropical tern species (Cramp 1985). -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
ASH Newsletter 45.Pub
THE AUSTRALIAN SOCIETY OF HERPETOLOGISTS INCORPORATED NEWSLETTER 45 2 3 History of Office Bearers Formation Committee (April 1964):- MJ Littlejohn (Convenor); State Reps IR Straughan (Qld), FJ Mitchell (SA), HG Cogger (NSW), G Storr (WA), RE Barwick (ACT), JW Warren (Vic), AK Lee (Editor). First AGM (23 August 1965):- President MJ Littlejohn, Vice-President NG Stephenson, Secretary-Treasurer AA Martin, Asst Secretary-Treasurer KJ Wilson, Ordinary Members FJ Mitchell and IR Straughan, Editor AK Lee. PRESIDENT:- MJ Littlejohn (1965-69); AK Lee (1969-70); HG Cogger (1971-73); J de Bavay (1974); H Heat- wole (1975-76); GC Grigg (1976-77); MJ Tyler (1978-79); GF Watson (1979-81); AA Martin (1981-82); RS Seymour (1982-83); R Shine (1983-84); GC Grigg (1984-86); J Coventry (1986-87); RE Barwick (1987-88); J Covacevich (1988-91); M Davies (1991-92); R Shine (1992-94); A Georges (1994-6); D Roberts (1996-98); M Bull (1998-9); R Swain (1999-2001); S Downes (2001-03); J Melville (2004-2005); J-M Hero (2005-2007); P Doherty (2007-2008); M Thompson (2008-2009); M Hutchinson (2009-) VICE-PRESIDENT:- NG Stephenson (1965-67); RE Barwick (1967-69); HG Cogger (1969-70); MJ Littlejohn (1971-72); MJ Tyler (1973); HG Cogger (1974); J de Bavay (1975-76); H Heatwole (1976-77); GC Grigg (1977 -79); MJ Tyler (1979-80); GF Watson (1981-82); AA Martin (1982-83); RS Seymour (1983-84); R Shine (1984- 86); GC Grigg (1986-87); J Coventry (1987-88); RE Barwick (1988-91); J Covacevich (1991-92); M Davies (1992-94); R Shine (1994-6); A Georges (1996-98); D Roberts (1998-99); M Bull(1999-2001); R Swain (2001- 2003); S Downes (2004-5); J Melville (2005-2007); J-M Hero (2007-2008); P Doherty (2008-2009); M Thomp- son (2009-) SECRETARY/TREASURER:- AA Martin (1965-67); GF Watson (1967-72); LA Moffatt (1973-75); J Caughley (1975-76); RWG Jenkins (1976-77); M Davies (1978-83); G Courtice (1983-87); J Wombey (1987-99); S Ke- ogh (1999-2003); N Mitchell (2004-5). -
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. -
Reproductionreview
REPRODUCTIONREVIEW The evolution of viviparity: molecular and genomic data from squamate reptiles advance understanding of live birth in amniotes James U Van Dyke, Matthew C Brandley and Michael B Thompson School of Biological Sciences, University of Sydney, A08 Heydon-Laurence Building, Sydney, New South Wales 2006, Australia Correspondence should be addressed to J U Van Dyke; Email: [email protected] Abstract Squamate reptiles (lizards and snakes) are an ideal model system for testing hypotheses regarding the evolution of viviparity (live birth) in amniote vertebrates. Viviparity has evolved over 100 times in squamates, resulting in major changes in reproductive physiology. At a minimum, all viviparous squamates exhibit placentae formed by the appositions of maternal and embryonic tissues, which are homologous in origin with the tissues that form the placenta in therian mammals. These placentae facilitate adhesion of the conceptus to the uterus as well as exchange of oxygen, carbon dioxide, water, sodium, and calcium. However, most viviparous squamates continue to rely on yolk for nearly all of their organic nutrition. In contrast, some species, which rely on the placenta for at least a portion of organic nutrition, exhibit complex placental specializations associated with the transport of amino acids and fatty acids. Some viviparous squamates also exhibit reduced immunocompetence during pregnancy, which could be the result of immunosuppression to protect developing embryos. Recent molecular studies using both candidate-gene and next-generation sequencing approaches have suggested that at least some of the genes and gene families underlying these phenomena play similar roles in the uterus and placenta of viviparous mammals and squamates. -
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.