Summary of Changes to the Conservation Status of Taxa in the 2008–11 New Zealand Threat Classification System Listing Cycle
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THE UNDERCROFT We Must Expire in Hope{ of Resurrection to Life Again
THE UNDERCROFT We must Expire in hope{ of Resurrection to Life Again 1 Editorial Illu{tration{ Daniel Sell Matthew Adams - 43 Jeremy Duncan - 51, 63 Anxious P. - 16 2 Skinned Moon Daughter Cedric Plante - Cover, 3, 6, 8, 9 Benjamin Baugh Sean Poppe - 28 10 101 Uses of a Hanged Man Barry Blatt Layout Editing & De{ign Daniel Sell 15 The Doctor Patrick Stuart 23 Everyone is an Adventurer E{teemed Con{ultant{ Daniel Sell James Maliszewski 25 The Sickness Luke Gearing 29 Dead Inside Edward Lockhart 41 Cockdicktastrophe Chris Lawson 47 Nine Summits and the Matter of Birth Ezra Claverie M de in elson Ma ia S t y a it mp ic of Authent Editorial Authors live! Hitler writes a children’s book, scratches his name off and hides it among the others. Now children grow up blue and blond, unable to control their minds, the hidden taint in friendly balloons and curious caterpillars wormed itself inside and reprogrammed them into literary sleeper agents ready to steal our freedom. The swine! We never saw it coming. If only authors were dead. But if authors were dead you wouldn’t be able to find them, to sit at their side and learn all they had to say on art and beautiful things, on who is wrong and who is right, on what is allowed and what is ugly and what should be done about this and that. We would have only words and pictures on a page, if we can’t fill in the periphery with context then how will we understand anything? If they don’t tell us what to enjoy, how to correctly enjoy it, then how will we know? Who is right and who is mad? Whose ideas are poisonous and wrong? Call to arms! Stop that! Help me! We must slather ourselves in their selfish juices. -
Keystone Species: the Concept and Its Relevance for Conservation Management in New Zealand
Keystone species: the concept and its relevance for conservation management in New Zealand SCIENCE FOR CONSERVATION 203 Ian J. Payton, Michael Fenner, William G. Lee Published by Department of Conservation P.O. Box 10-420 Wellington, New Zealand Science for Conservation is a scientific monograph series presenting research funded by New Zealand Department of Conservation (DOC). Manuscripts are internally and externally peer-reviewed; resulting publications are considered part of the formal international scientific literature. Titles are listed in the DOC Science Publishing catalogue on the departmental website http:// www.doc.govt.nz and printed copies can be purchased from [email protected] © Copyright July 2002, New Zealand Department of Conservation ISSN 11732946 ISBN 047822284X This report was prepared for publication by DOC Science Publishing, Science & Research Unit; editing by Lynette Clelland and layout by Ruth Munro. Publication was approved by the Manager, Science & Research Unit, Science Technology and Information Services, Department of Conservation, Wellington. CONTENTS Abstract 5 1. Introduction 6 2. Keystone concepts 6 3. Types of keystone species 8 3.1 Organisms controlling potential dominants 8 3.2 Resource providers 10 3.3 Mutualists 11 3.4 Ecosystem engineers 12 4. The New Zealand context 14 4.1 Organisms controlling potential dominants 14 4.2 Resource providers 16 4.3 Mutualists 18 4.4 Ecosystem engineers 19 5. Identifying keystone species 20 6. Implications for conservation management 21 7. Acknowledgements 22 8. References 23 4 Payton et al.Keystone species: the concept and its relevance in New Zealand Keystone species: the concept and its relevance for conservation management in New Zealand Ian J. -
Phthiraptera: Philopteridae) from Peruvian Ovenbirds (Passeriformes: Furnariidae)
PROC. ENTOMOL. soc. WASH. 97(4), 1995, pp. 839-844 A NEW GENUS AND THREE NEW SPECIES OF CHEWING LICE (PHTHIRAPTERA: PHILOPTERIDAE) FROM PERUVIAN OVENBIRDS (PASSERIFORMES: FURNARIIDAE) ROGER D. PRICE AND DALE H. CLAYTON (RDP) Department of Entomology, Oklahoma State University, Stillwater, Oklahoma 74078 (Current address) 4622 Kinkead Avenue, Fort Smith, Arkansas 72903; (DHC) Department of Zoology, University of Oxford, South Parks Road, Oxford OXI 3PS, England. Abstract.-The new genus Furnariphilus is described to include three new species from Peruvian hosts within the passerine family Fumariidae, subfamily Fumariinae: F. pagei, the type species of the genus, from Furnarius leucopus Swainson; F. griffithsi from Sclerurus mexican us Sclater; and F. parkeri from Sclerurus caudacutus (Vieillot). Key Words: Ectoparasites, Peru, Furnariphilus, Fumariinae, Bird Clayton et aL (1992) published a survey first time they are used. Host classification of chewing lice collected in 1985 from a follows that of Sibley and Monroe (1990). wide array of Peruvian bird taxa. During Holotypes of the new species will be de this project, a number of undescribed louse posited in The Field Museum (Chicago) taxa were collected from hosts in the parv and paratypes, as numbers allow, will be orders Thamnophilida and Fumariida (Pas located in the collections of that museum seriformes). These taxa included a new spe and those of the National Museum of Nat cies placed by Price and Clayton (1989) in ural History (Washington, D.C.), Oklahoma a new genus of Menoponidae, Kaysius. and State University (Stillwater), and the Uni seven new species described by Price and versity of Minnesota (St. Paul). -
Conservation
SCIENCE OF ECOLOGY AND ART OF CONSERVATION Protection of native species by applying scientific principles of conservation can save New Zealand’s threatened flora and fauna from extinction. Indeed, safeguarding species diversity and abundance will ensure today’s gene pool contributes to the ability of species’ to adapt in tomorrow’s changing environment. Greater biodiversity thereby enhances opportunities for the future evolution of new species. Ecological degradation began with the arrival of humans (circa 1280 AD), along with their cargo of predators to this archipelago. Many species were lost when Polynesians and Europeans respectively destroyed 32% and 38% of the country’s natural forests. Polynesians caused the extinction of >70 native species and European’s another 12 species. Prolonged hunting and habitat loss precipitated extinction of ~58 bird species*. Introduced predators quickly gained supremacy over smaller avian and insect species. Kiore (Rattus exulans) alone led to the loss of ~23 small bird, bat, reptile and invertebrate species. The worldwide IUCN Red List contains 784 extinct species, of which 27 have been lost in the past 20 years. The Red List’s threatened species includes 45 New Zealand birds, including the North Island kokako, kaka, kiwi, kakapo and mohua. The country’s birds are prone to predation and their numbers in most cases continue to decline (Table 1). This includes extinction of the South Island kokako, last reported to occur in Teal Creek, Mount Aspiring National Park in 1967 (Fig. 1). North Island kokako (Callaeas cinerea wilsoni) with their aquamarine wattle are few, and limited mostly to the Mainland Island Restoration Project, Otamatuna, Te Urewera National Park. -
Co-Extinct and Critically Co-Endangered Species of Parasitic Lice, and Conservation-Induced Extinction: Should Lice Be Reintroduced to Their Hosts?
Short Communication Co-extinct and critically co-endangered species of parasitic lice, and conservation-induced extinction: should lice be reintroduced to their hosts? L AJOS R ÓZSA and Z OLTÁN V AS Abstract The co-extinction of parasitic taxa and their host These problems highlight the need to develop reliable species is considered a common phenomenon in the current taxonomical knowledge about threatened and extinct global extinction crisis. However, information about the parasites. Although the co-extinction of host-specific conservation status of parasitic taxa is scarce. We present a dependent taxa (mutualists and parasites) and their hosts global list of co-extinct and critically co-endangered is known to be a feature of the ongoing wave of global parasitic lice (Phthiraptera), based on published data on extinctions (Stork & Lyal, 1993; Koh et al., 2004; Dunn et al., their host-specificity and their hosts’ conservation status 2009), the magnitude of this threat is difficult to assess. according to the IUCN Red List. We list six co-extinct Published lists of threatened animal parasites only cover and 40 (possibly 41) critically co-endangered species. ixodid ticks (Durden & Keirans, 1996; Mihalca et al., 2011), Additionally, we recognize 2–4 species that went extinct oestrid flies (Colwell et al., 2009), helminths of Brazilian as a result of conservation efforts to save their hosts. vertebrates (Muñiz-Pereira et al., 2009) and New Zealand Conservationists should consider preserving host-specific mites and lice (Buckley et al., 2012). Our aim here is to lice as part of their efforts to save species. provide a critical overview of the conservation status of parasitic lice. -
Husbandry of the Carnivorous Land Snail, Powelliphanta Augusta (Gastropoda: Pulmonata: Rhytdidae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by ResearchArchive at Victoria University of Wellington Husbandry of the Carnivorous Land Snail, Powelliphanta augusta (Gastropoda: Pulmonata: Rhytdidae) By Thomas Edward Allan A thesis submitted to the Victoria University of Wellington in fulfillment of the requirements for the degree of Master of Science in Ecological Restoration Victoria University of Wellington 2010 1 Abstract Key aspects of the captive husbandry of Powelliphanta augusta, a newly-described New Zealand land snail are investigated: how they should be managed and fed to provide individuals for release, and how a long-term captive population can be maintained as an insurance against extinction in the wild. This project arises from almost all members of this species having been brought into captivity due to their displacement in the wild by an opencast coalmine. Powelliphanta (F: Rhytididae) is a genus of endemic carnivorous snails, which includes 10 species, 27 subspecies and numerous undescribed taxa. As well as its diversity, Powelliphanta is renowned for the large size of its members (up to 90mm diameter) and their attractively-patterned shells. Most taxa are threatened due to habitat loss and predation by introduced mammalian predators. The study commences with a literature review to refine husbandry methods and to assess requirements for captive breeding of snails. From this review investigations are made into stocking densities, substrate, reproductive biology, body condition and growth of the P. augusta captive population. To determine an appropriate stocking density for P. augusta groups of six snails were kept at two densities; with either 720cm2, or 1440cm2 per group. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Direct Impacts of Seabird Predators on Island Biota Other Than Seabirds D.R
4 Direct Impacts of Seabird Predators on Island Biota other than Seabirds D.R. Drake, T.W. Bodey, J.e. Russell, D.R. Towns, M. Nogales, and L. Ruffino Introduction "... I have not found a single instance .. , ofa terrestrial mammal inhabiting an island situated above 300 miles from a continent or great continental island; and many islands situated at a much less distance are equally barren:' (DARWIN 1859) "He who admits the doctrine of special creation ofeach species, will have to admit, that a sufficient number ofthe best adapted plants and animals have not been created on oceanic islands; for man has unintentionally stocked them from various sources far more fully and perfectly than has nature:' (DARWIN 1859) Since Darwin's time, islands have been celebrated for having highly endemic floras and faunas, in which certain taxonomic groups are typically overrepresented or underrepresented relative to their abundance on the nearest continents (Darwin 1859, Wallace 1911, Carlquist 1974, Whittaker and Fermindez-Palacios 2007). Sadly, island endemics in many taxonomic groups have suffered a disproportionately large number ofthe world's extinctions, and introduced mammals have frequently been implicated in their decline and disappearance (Vitousek 1988, Flannery and Schouten 2001, Drake et al. 2002, Courchamp et al. 2003, Steadman 2006). Of the many mammalian predators introduced to islands, those having the most important impact on seabirds are cats, foxes, pigs, rats, mice, and, to a lesser extent, dogs and mongooses (discussed extensively in Chapter 3). These predators can be divided into two groups: superpredators and mesopredators. Superpredators (e.g., cats and foxes) are carnivores, relatively large, and able to consume all life stages oftheir prey (including other, smaller predator species). -
The Mallophaga of New England Birds James Edward Keirans Jr
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 1966 THE MALLOPHAGA OF NEW ENGLAND BIRDS JAMES EDWARD KEIRANS JR. Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation KEIRANS, JAMES EDWARD JR., "THE MALLOPHAGA OF NEW ENGLAND BIRDS" (1966). Doctoral Dissertations. 834. https://scholars.unh.edu/dissertation/834 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received 67—163 KEIRANS, Jr., James Edward, 1935— THE MALLOPHAGA OF NEW ENGLAND BIRDS. University of New Hampshire, Ph.D., 1966 E n tom ology University Microfilms, Inc., Ann Arbor, Michigan THE MALLOPHAGA OF NEW ENGLAND BIRDS BY JAMES E.° KEIRANS, -TK - A. B,, Boston University, i960 A. M., Boston University, 19^3 A THESIS Submitted to The University of New Hampshire In Partial Fulfillment of The Requirements for the Degree of Doctor of Philosophy Graduate School Department of Zoology June, 1966 This thesis has been examined and approved. May 12i 1966 Date ACKNOWLEDGEMENT I wish to express my thanks to Dr. James G. Conklin, Chairman, Department of Entomology and chairman of my doctoral committee, for his guidance during the course of these studies and for permission to use the facilities of the Entomology Department. My grateful thanks go to Dr. Robert L. -
Native New Zealand Land Birds Present During the Holocene
New Zealand plant and vertebrate species known to be extinct Source: Tennyson, Alan, and Paul Martinson. Extinct birds of New Zealand. Wellington: Te Papa Press, 2006. New Zealand Plant Conservation Network, http://www.nzpcn.org.nz/nz_threatenedplants/threatened_list.asp (last accessed 7 June 2007). Group Common name Scientific name Distribution Cause of extinction Last known Plants a coastal cress Lepidium obtusatum North Island Introduced browsers 1950 a prostrate shrub Logania depressa North Island Habitat loss (hydro dam) and 1847 weed infestation a limestone forget-me-not Myosotis traversii var. South Island Over-collection, weed Early 1900s cinerascens invasion a stitchwort Stellaria elatinoides North and South Habitat loss, weed invasion 1940s islands Adams mistletoe Trilepidea adamsii North Island Habitat loss, lost pollinators 1954 and dispersers, possum browsing, over-collecting Bats Greater short-tailed bat Mystacina robusta North, South and Introduced predators 1967 Stewart islands Frogs Aurora frog Leiopelma auroraensis South Island Introduced predators Pre-European Markham's frog Leiopelma markhami North and South Introduced predators Pre-European islands Waitomo frog Leiopelma North Island Introduced predators Pre-European waitomoensis Lizards Northland skink Cyclodina northlandi North Island Introduced predators Pre-European (skinks and geckos) Downloaded from Te Ara – The Encyclopedia of New Zealand All rights reserved http://www.TeAra.govt.nz 2 Narrow-bodied skink Oligosoma North Island Introduced predators Pre-European -
Northland CMS Volume I
CMS CONSERVATION MANAGEMENT STRATEGY N orthland 2014–2024, Volume I Operative 29 September 2014 CONSERVATION106B MANAGEMENT STRATEGY NORTHLAND107B 2014–2024, Volume I Operative108B 29 September 2014 Cover109B image: Waikahoa Bay campsite, Mimiwhangata Scenic Reserve. Photo: DOC September10B 2014, New Zealand Department of Conservation ISBN10B 978-0-478-15017-9 (print) ISBN102B 978-0-478-15019-3 (online) This103B document is protected by copyright owned by the Department of Conservation on behalf of the Crown. Unless indicated otherwise for specific items or collections of content, this copyright material is licensed for re- use under the Creative Commons Attribution 3.0 New Zealand licence. In essence, you are free to copy, distribute and adapt the material, as long as you attribute it to the Department of Conservation and abide by the other licence terms. To104B view a copy of this licence, visit http://creativecommons.org/licenses/by/3.0/nz/U U This105B publication is produced using paper sourced from well-managed, renewable and legally logged forests. Contents802B 152B Foreword803 7 Introduction804B 8 Purpose809B of conservation management strategies 8 CMS810B structure 9 CMS81B term 10 Relationship812B with other Department of Conservation strategic documents and tools 10 Relationship813B with other planning processes 11 Legislative814B tools 11 Exemption89B from land use consents 11 Closure890B of areas and access restrictions 11 Bylaws891B and regulations 12 Conservation892B management plans 12 International815B obligations 12 Part805B -
Skeletal Variation in Extant Species Enables Systematic Identification of New Zealand's Large, Subfossil Diplodactylids
Scarsbrook et al. BMC Ecol Evo (2021) 21:67 BMC Ecology and Evolution https://doi.org/10.1186/s12862-021-01808-7 RESEARCH Open Access Skeletal variation in extant species enables systematic identifcation of New Zealand’s large, subfossil diplodactylids Lachie Scarsbrook1*, Emma Sherratt2, Rodney A. Hitchmough3 and Nicolas J. Rawlence1 Abstract New Zealand’s diplodactylid geckos exhibit high species-level diversity, largely independent of discernible osteologi- cal changes. Consequently, systematic afnities of isolated skeletal elements (fossils) are primarily determined by comparisons of size, particularly in the identifcation of Hoplodactylus duvaucelii, New Zealand’s largest extant gecko species. Here, three-dimensional geometric morphometrics of maxillae (a common fossilized element) was used to determine whether consistent shape and size diferences exist between genera, and if cryptic extinctions have occurred in subfossil ‘Hoplodactylus cf. duvaucelii’. Sampling included 13 diplodactylid species from fve genera, and 11 Holocene subfossil ‘H. cf. duvaucelii’ individuals. We found phylogenetic history was the most important predictor of maxilla morphology among extant diplodactylid genera. Size comparisons could only diferentiate Hoplodactylus from other genera, with the remaining genera exhibiting variable degrees of overlap. Six subfossils were positively identifed as H. duvaucelii, confrming their proposed Holocene distribution throughout New Zealand. Conversely, fve subfossils showed no clear afnities with any modern diplodactylid genera, implying either increased morphological diversity in mainland ‘H. cf. duvaucelii’ or the presence of at least one extinct, large, broad-toed diplodactylid species. Keywords: Diplodactylidae, Ecomorphology, Geometric morphometrics, Hoplodactylus duvaucelii, Taxonomy Background (e.g. coloration and scalation), with interspecifc skeletal New Zealand’s lizard fauna is characteristic of isolated variation rarely analysed.