Pateke Survival Guide 1 Pāteke Flocking on a Tidally Influenced Section of Stream Above an Estuary
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A 2010 Supplement to Ducks, Geese, and Swans of the World
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "The World’s Waterfowl in the 21st Century: A 2010 Supplement to Ducks, Geese, and Swans of the World" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 20. https://digitalcommons.unl.edu/biosciducksgeeseswans/20 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. The World’s Waterfowl in the 21st Century: A 200 Supplement to Ducks, Geese, and Swans of the World Paul A. Johnsgard Pages xvii–xxiii: recent taxonomic changes, I have revised sev- Introduction to the Family Anatidae eral of the range maps to conform with more current information. For these updates I have Since the 978 publication of my Ducks, Geese relied largely on Kear (2005). and Swans of the World hundreds if not thou- Other important waterfowl books published sands of publications on the Anatidae have since 978 and covering the entire waterfowl appeared, making a comprehensive literature family include an identification guide to the supplement and text updating impossible. -
Mallard (Anas Platyrhynchos) New Zealand Scaup/Pāpango (Aythya
DUCK DESCRIPTION HABITAT, HABITS AND OTHER FACTS Mallard (Anas platyrhynchos) The mallard is a dabbling duck. Mallards were introduced to New Zealand. They live in wetlands all over the country and congregate in groups or flocks of varying sizes. They eat water plants and small animals. © Richard Bartz/CC 2.5 © Richard Bartz/CC Mallards have bright orange legs and This species is the main ancestor of most feet, orange and brown bills and a blue breeds of domesticated ducks. speculum edged with white at both the front and back. The mallard is considered an invasive pest Drakes have a glossy green head and are and is the most common duck in grey on their wings and belly. Hens have New Zealand. mainly brown-speckled plumage. © Copyright. 2017. University of Waikato. All rights reserved. | www.sciencelearn.org.nz DUCK DESCRIPTION HABITAT, HABITS AND OTHER FACTS New Zealand scaup/pāpango (Aythya novaeseelandiae) The scaup/pāpango is the only true diving duck in New Zealand. They are endemic to New Zealand. They are found in many lakes and rivers across mainland New Zealand, especially on large, deep, freshwater lakes. They are becoming increasingly common also on shallow lowland lakes, slow-flowing rivers and saltwater and often congregate in © Raewyn Adams/NZ Birds Online Adams/NZ © Raewyn sheltered areas. Both sexes of scaup/pāpango are a dark Most of their food is obtained by diving and brown/black colour. includes snails, caddisfly larvae and plant A white wing bar can be seen while they material. are flying. Scaup/pāpango are also known as black teal, Male scaup have yellow eyes and a matapōuri, tītīpōrangi or raipo. -
Distributions of New Zealand Birds on Real and Virtual Islands
JARED M. DIAMOND 37 Department of Physiology, University of California Medical School, Los Angeles, California 90024, USA DISTRIBUTIONS OF NEW ZEALAND BIRDS ON REAL AND VIRTUAL ISLANDS Summary: This paper considers how habitat geometry affects New Zealand bird distributions on land-bridge islands, oceanic islands, and forest patches. The data base consists of distributions of 60 native land and freshwater bird species on 31 islands. A theoretical section examines how species incidences should vary with factors such as population density, island area, and dispersal ability, in two cases: immigration possible or impossible. New Zealand bird species are divided into water-crossers and non-crossers on the basis of six types of evidence. Overwater colonists of New Zealand from Australia tend to evolve into non-crossers through becoming flightless or else acquiring a fear of flying over water. The number of land-bridge islands occupied per species increases with abundance and is greater for water-crossers than for non-crossers, as expected theoretically. Non-crossers are virtually restricted to large land-bridge islands. The ability to occupy small islands correlates with abundance. Some absences of species from particular islands are due to man- caused extinctions, unfulfilled habitat requirements, or lack of foster hosts. However, many absences have no such explanation and simply represent extinctions that could not be (or have not yet been) reversed by immigrations. Extinctions of native forest species due to forest fragmentation on Banks Peninsula have especially befallen non-crossers, uncommon species, and species with large area requirements. In forest fragments throughout New Zealand the distributions and area requirements of species reflect their population density and dispersal ability. -
Handbook of Waterfowl Behavior: Tribe Anatini (Surface-Feeding Ducks)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Handbook of Waterfowl Behavior, by Paul Johnsgard Papers in the Biological Sciences January 1965 Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks) Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/bioscihandwaterfowl Part of the Ornithology Commons Johnsgard, Paul A., "Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks)" (1965). Handbook of Waterfowl Behavior, by Paul Johnsgard. 16. https://digitalcommons.unl.edu/bioscihandwaterfowl/16 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Handbook of Waterfowl Behavior, by Paul Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Subfamily Anatinae 125 Aix. During extreme excitement the male will often roll his head on his back, or even bathe. I have not observed Preening-behind-the- wing, but W. von de Wall (pers. comm.) has observed a male per- form it toward a female. Finally, Wing-flapping appears to be used as a display by males, and it is especially conspicuous because each sequence of it is ended by a rapid stretching of both wings over the back in a posture that makes visible the white axillary feathers, which contrast sharply with the black underwing surface. Copulatory behavior. Precopulatory behavior consists of the male swimming up to the female, his neck stretched and his crest de- pressed, and making occasional Bill-dipping movements. He then suddenly begins to perform more vigorous Head-dipping movements, and the female, if receptive, performs similar Bill-dipping or Head- dipping movements. -
Brown Teal Captive Management Plan
Brown Teal Captive Management Plan THREATENED SPECIES OCCASIONAL PUBLICATION NO. 15 Brown Teal Captive Management Plan THREATENED SPECIES OCCASIONAL PUBLICATION NO. 15 Grant Dumbell Published by Biodiversity Recovery Unit Department of Conservation P.O. Box 10-420 Wellington, New Zealand Cover photograph: brown teal mother and young. Photograph copyright New Zealand Herald. Reprinted by permission. © March 2000, Department of Conservation ISSN 1170-3709 ISBN 047821936-9 Cataloguing-in-Publication data Dumbell, G. (Grant) Brown teal captive management plan / G. Dumbell. Wellington, N.Z. : Dept of Conservation, 2000. 1 v. ; 30 cm. (Threatened species occasional publication, 1170-3709 ; no. 15.) Includes bibliographical references. 0478219369 1. Endangered birds--New Zealand--Management. 2. Brown teal-- Captive management--New Zealand. 3. Anas chlorotis. I. Dumbell, G. (Grant). II. Series : Threatened species occasional publication ; no. 15. CONTENTS Abstract 5 1. Introduction 6 1.1 Taxonomy of brown teal 6 1.2 Conservation status of brown teal 6 1.3 History of brown teal in captivity 7 Table 1. Annual breeding results from the Ducks Unlimited New Zealand Inc. Operation Pateke 10 2. Goal, objectives, and context of brown teal captive management 12 2.1 Context of captive management 12 2.2 Goal of captive management 13 2.3 Objectives of captive management 13 2.4 Time frame of Captive Management Plan 14 3. Captive management strategy 15 3.1 Task time frames and review 15 Figure 1. Suggested timeframes for completion of identified tasks within -
Phylogeny Biogeography, and Taxonomy of Australasian
The Auk 117(1):154-163, 2000 PHYLOGENY, BIOGEOGRAPHY, AND TAXONOMY OF AUSTRALASIAN TEALS MARTYN KENNEDY 1 AND HAMISH G. SPENCER Departmentof Zoology,University of Otago,P.O. Box 56, Dunedin,New Zealand ABSTRACT.--Thetaxonomy of the Australasianteals has been particularly unstable. Aus- tralasianGrey Teal (Anasgracilis) and ChestnutTeal (A. castanea)are widely viewed asspe- cificallydistinct, but the taxonomyof theNew Zealandteals remains unsettled. Because con- servationstatus is affectedby taxonomicrank, it is importantto resolvethe statusof the rare subantarcticteals. To estimatephylogenetic relationships of teals,we sequencedthree mi- tochondrialDNA genes(12S, and ATPase6 and 8). The resultantphylogeny unequivocally groupsthe ChestnutTeal with the GreyTeal, rather than with the New Zealandteals as has traditionally been held (Fleming 1953). A greater level of sequencedivergence occurred within the New Zealandteals than betweenthe Grey and Chestnutteals. This diversity,to- getherwith morphologicaland behavioraldifferences, implies that the New Zealandteals shouldbe accordedspecific status as A. aucklandica,A. nesiotis,and A. chlorotis.Although it is most likely that the teal that colonizedthe AucklandIslands and CampbellIslands orig- inated in New Zealand, our data do not allow us to determine whether the ancestors of the CampbellIsland Teal came from mainlandNew Zealandor the AucklandIslands. This un- certaintyarises because, as our data show,the colonizationevents were separatedby a short period of time. Received25 November1998, accepted 16 June1999. F•VE EXTANT TEALS inhabit the Australasian 1990).The brown-plumagedteals (i.e. all teals region and provide an interesting example of exceptthe Grey Teal)all existin allopatry.The speciationin insularSouthern Hemisphere wa- Auckland Island Teal (A. aucklandica)and terfowl (see Livezey 1990). Grey Teal (Anas CampbellIsland Teal (A. nesiotis)occur only on gracilis),which are small and drab, are wide- their respectivesubantarctic island groups (see spreadthroughout Australia. -
Hybridisation in the Last Remaining Individuals Of
Records of the Canterbury Museum, 2017 Vol. 31: 159–165 © Canterbury Museum 2017 159 Hybridisation in the last remaining individuals of the extinct Fiordland population of Brown Teal (Anas chlorotis) Theresa L Cole1,2 and Jamie R Wood1 1Landcare Research, PO Box 69040, Lincoln 7640, New Zealand Email: [email protected] 2Department of Zoology, University of Otago, PO Box 56, Dunedin 9054, New Zealand The New Zealand endemic Brown Teal (Anas chlorotis Gray, 1845) was once widespread on the three main islands of New Zealand, some offshore islands and the Chatham Islands. Hunting and drainage of wetlands during the early years of European colonisation, however, resulted in a severely reduced range for the species and by 1990, the last remaining wild populations were on Great Barrier Island, and in eastern Northland and Fiordland. However, by 2007, the Fiordland population of Brown Teal was assumed extinct. The potential role of hybridisation with Mallard (Anas platyrhynchos Linnaeus, 1758) and Grey Duck (Anas superciliosa Gmelin, 1789) in the decline of the Fiordland population of Brown Teal has previously been recognised, though specimen details and tissue voucher samples associated with the DNA sequences were not retained. Here, we provide new mitochondrial DNA sequences from four specimens of Fiordland Brown Teal registered in the collections of Canterbury Museum. The results provide evidence for hybridisation with Mallard/ Grey Duck in all four individuals, and support previous suggestions that hybridisation could have played a role in the decline of the Fiordland Brown Teal population. Keywords: Conservation, genetics, Mallard, museum, voucher specimens Introduction The New Zealand endemic Brown Teal Anas( Teal were on Great Barrier Island, and in eastern chlorotis Gray, 1845), or pāteke, was formerly Northland and Fiordland (Gemmell and Flint widespread on the three main islands of New 2000). -
Ducks, Geese, and Swans of the World by Paul A
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Ducks, Geese, and Swans of the World by Paul A. Johnsgard Papers in the Biological Sciences 2010 Ducks, Geese, and Swans of the World: Contents, Preface, & Introduction Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/biosciducksgeeseswans Part of the Ornithology Commons Johnsgard, Paul A., "Ducks, Geese, and Swans of the World: Contents, Preface, & Introduction" (2010). Ducks, Geese, and Swans of the World by Paul A. Johnsgard. 2. https://digitalcommons.unl.edu/biosciducksgeeseswans/2 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Ducks, Geese, and Swans of the World by Paul A. Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. DUCKS, GEESE, and SWANS of the World Paul A. Johnsgard Revised Edition Ducks, Geese, and Swans of the World By Paul A. Johnsgard The only one-volume comprehensive survey of the family Anatidae available in English, this book combines lavish illustration with the most recent information on the natural history, current distribution and status, and identification of all the species. After an introductory discussion of the ten tribes of Anatidae, separate accounts follow for each of the nearly 150 recognized species. These include scientific and vernacular names (in French, German, and Spanish as well as English), descrip- tions of the distribution of all recognized subspecies, selected weights and mea- surements, and identification criteria for both sexes and various age classes. -
ANSERIFORMES Taxon Advisory Group Regional Collection Plan 3Rd Edition • 2020 - 2025
ANSERIFORMES Taxon Advisory Group Regional Collection Plan 3rd Edition • 2020 - 2025 Edited by Photo by Pinola Conservancy Keith Lovett, Anseriformes TAG Chair Buttonwood Park Zoo Table of Contents Acknowledgements 03 TAG Operational Structure 04 TAG Steering Committee and Advisors: Table 1 05 TAG Definition 06 TAG Mission 06 TAG Vision 06 TAG Strategic Planning Overview 07 TAG Goals Sustainability 08 Conservation 09 Husbandry and Welfare 09 Educational Waterfowl Awareness and Program Support 10 TAG Taxonomy 11 TAG Taxonomy: Table 2 12 Conservation Status of Anseriformes Overview 13 Conservation Status of Anseriformes: Table 3 14 RCP History and Program Designation Program Management Designation 20 Additional Management Designation 21 Selection Criteria Selection Criteria Overview 22 Decision Tree Selection Criteria Categories 23 Proposed EAZA Waterfowl TAG European Endangered 24 Species Program (EEP) Species Anseriformes Decision Tree: Table 4 25 Anseriformes TAG Selection Criteria / Decision Tree: Table 5 26 Anseriformes TAG Selection Criteria / Decision Tree Summary 33 Space Assessment Space Assessment Overview 34 Space Survey Accountability:Responding Insititutions: Table 6 35 Space Survey Accountability: Non-responding Insititutions: Table 7 37 Space Survey Results and Target Size: Table 8 38 Regional Anseriformes Populations: Table 9 39 Summary Table 46 Non-Recommended Species Replacement Overview 47 Non-Recommended Species Replacement Chart: Table 11 48 Management Update: Table 12 51 SSP Five Year Goals and Essential Actions 53 -
Resource Selection by New Zealand Pāteke/Brown Teal (Anas Chlorotis) at Two North Island Locations
Resource Selection by New Zealand Pāteke/Brown Teal (Anas chlorotis) at two North Island Locations Debbie Maree Lewis A thesis submitted for the Degree of Doctor of Philosophy in Zoology at the University of Otago, Dunedin, New Zealand. July 2017 Pāteke family, Port Fitzroy, Great Barrier Island. Image: Keith Payne Summary Identification of the resources an animal is selecting allows us to understand how animals use what is available to meet their requirements for survival, growth, and reproduction. Understanding the process by which selections are made is essential for successful conservation management as it allows us to investigate the impacts of modified landscapes and to develop informed policies and remedial measures to mitigate current and future negative impacts. However, despite the important role for conservation management, the quantification of resource selection is not always straight forward. Obtaining and interpreting resource selection information can be problematic for many species (Hebblewhite and Haydon, 2010, Aarts et al., 2008), potentially leaving important management questions unanswered. The New Zealand pāteke/ brown teal (Anas chlorotis) are a cryptic, predominantly nocturnal dabbling duck, that inhabits wetland areas. Formerly widespread and numerous throughout New Zealand, pāteke have undergone a decline described as ‘arguably the most dramatic of any New Zealand species’ (Williams, 2001). Pāteke are ranked as ‘nationally endangered’ by the Department of Conservation (O'Connor et al., 2007) and have been listed as ‘endangered’ on the International Union for the Conservation of Nature (IUCN) Red List since 2000 (IUCN website http://www.iucnredlist.org). Of particular concern, is the alarming juvenile starvation rate within the pāteke population at Great Barrier Island (Watts et al., 2016). -
GREAT BARRIER ISLAND WILDLIFE SURVEY by C.C
TANE 27, 1981 GREAT BARRIER ISLAND WILDLIFE SURVEY by C.C. Ogle New Zealand Wildlife Service, Department of Internal Affairs, Wellington SUMMARY Sixty-two species of birds (55 land birds, including migratory waders) were recorded in a survey of Great Barrier Island, March—April 1980. In addition, the following land-fauna were found: nine species of lizard, two species of frog, two species of Rhytidid molluscs, and eight species of introduced wild mammals. Included in these totals are the first known records from Great Barrier Island of spotless crake {Porzana tabuensis plumbed), Hochstetter's frog (Leiopelma hochstetteri), the mollusc Rhytida greenwoodi, and a lizard which was possibly Cyclodina oliveri. The current status of species not found by this survey but recorded by earlier authors (Bell and Brathwaite 1964, Bell 1976, Harris 1980, Hutton 1868, Powell 1938, Taylor 1976) is discussed. INTRODUCTION At the request of the Department of Lands and Survey, Auckland, the Fauna Survey Unit of the New Zealand Wildlife Service surveyed Great Barrier Island, as a contribution to a multi-disciplinary land-use study of the island. The wildlife survey was made from 26 March to 12 April 1980 although the author remained until 15 April 1980. A preliminary report of this survey (Ogle 1980) was prepared for the Department of Lands and Survey, and was also distributed to some other statutory bodies and individuals. (a) Location and land-form Great Barrier Island, 28 500 hectares in area, lies across the entrance to the Hauraki Gulf, about 80 km north-east of Auckland and 20 km north of Coromandel Peninsula (Fig. -
New Zealand North Island Endemics 16Th November to 24Th November 2021 (9 Days) South Island Endemics 24Th November to 3Rd December 2021 (10 Days)
New Zealand North Island Endemics 16th November to 24th November 2021 (9 days) South Island Endemics 24th November to 3rd December 2021 (10 days) Whitehead by Adam Riley New Zealand supports a host of unusual endemic land birds and a rich assemblage of marine birds and mammals. Our North Island tour is designed to seek almost every possible endemic and take full RBL New Zealand – South Island Endemics & Extension Itinerary 2 advantage of fabulous scenery. Beginning in Auckland, we target North Island Brown Kiwi, Whitehead and North Island Saddleback as well as a visit to the fabled Tiritiri Matangi Island where we will bird this predator-free reserve for the prehistoric South Island Takahe, strange North Island Kokako and Stitchbird, before combing the Miranda shoreline for the bizarre Wrybill and numerous waders. A pelagic excursion then takes place in the Hauraki Gulf in search of the Black and Cook’s Petrel, Buller’s Flesh-footed and Fluttering Shearwater. From here we visit the scenic Tongariro National Park in the centre of the North Island where we check fast-flowing streams for the rare Blue Duck while nearby forests hold Rifleman and Tomtit. We finish our time on the North Island visiting the famous Zealandia Reserve searching for the endangered Little Spotted Kiwi, New Zealand Falcon, Red-crowned Parakeet, New Zealand Kaka and Stitchbird We start our South Island tour in the beautiful grasslands of the Mackenzie region of the South Island where we will take in the beauty of the Southern Alpine rang, while looking for the critically endangered Black Stilt, before hiking through pristine Red Beech forest surrounded by breath-taking glacier-lined mountains, where the massive Kea (an Alpine parrot) can be found.