Native Frog (Leiopelma Spp.) Recovery Plan
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NOTORNIS Journal of the Ornithological Society of New Zealand Volume 25 Part 4 December 1978 OFFICERS 1978 - 79 President - Mr. B. D. BELL, Wildlife Service, Dept. of Internal Affairs, Private Bag, Wellington Vice-president - Mr. M. L. FALCONER, 188 Miromiro Road, Normandale, Lower Hutt Editor - Mr. B. D. HEATHER, 10 Jocelyn Crescent, Silverstrearn Treasurer - Mr. H. W. M. HOGG, P.O. Box 3011, Dunedin Secretary - Mr. H, A. BEST, Wildlife Service, Dept. of Internal Affairs, Wellington Council Members: Dr. BEN D. BELL, 45 Gurney Road, Belmont, Lower Hutt Mrs. B. BROWN, 39 Red Hill Road, Papakura Dr. P. C. BULL, 131 Waterloo Road, Lower Hutt Mr D. E. CROCKETT, 21 McMillan Avenue, Kamo, Whangarei Mr. F. C. KINSKY, 338 The Parade, Island Bay, Wellington 5 Mrs. S. M. REED, 4 Mamaku Street, Auckland 5 Mr. R. R. SUTTON, Lorneville, No. 4 R.D., Invercargill Conveners and Organisers: Rare Birds Committee (Acting): Mr. B. D. BELL Beach Patrol: Mr. C. R. VEITCH, Wildlife Service, Dept. of Internal Affairs, P.O. Box 2220, Auckland Card Committee: Mr. R. N. THOMAS, 25 Ravenswood Drive, Forest Hill, Auckland 10 Field Investigation Committee: Mr. B. D. BELL ' Librarian: Miss A. J. GOODWIN, R.D. 1, Clevedon Nest Records: Mr. D. E. CROCKETT Recording (including material for Classified Surnmarised Notes) : Mr. R. B. SIBSON, 26 Entrican Avenue, Remuera, Auckland Representative on Member Bodies' Committee of Royal Society of N.Z.: Mr. B. D. BELL Assistant Editor: Mr A. BLACKBURN, 10 Score Road, Gisborne Editor of OSNZ News: Mr P. SAGAR, 2/362 Hereford St., Christchurch SUBSCRIPTIONS AND MEMBERSHIP Annual Subscription: Ordinary membership $6; Husband/Wife member- ship $9; Life membership $120 (age over 30); Junior member- ship (age under 20) $4.50; Family membership (one Notornis er household) other members of a family living in one house iold where one is already a member $3; Institutional subscrip tions $10; overseas subscriptions $2.00 extra. -
Council Agenda - 26-08-20 Page 99
Council Agenda - 26-08-20 Page 99 Project Number: 2-69411.00 Hauraki Rail Trail Enhancement Strategy • Identify and develop local township recreational loop opportunities to encourage short trips and wider regional loop routes for longer excursions. • Promote facilities that will make the Trail more comfortable for a range of users (e.g. rest areas, lookout points able to accommodate stops without blocking the trail, shelters that provide protection from the elements, drinking water sources); • Develop rest area, picnic and other leisure facilities to help the Trail achieve its full potential in terms of environmental, economic, and public health benefits; • Promote the design of physical elements that give the network and each of the five Sections a distinct identity through context sensitive design; • Utilise sculptural art, digital platforms, interpretive signage and planting to reflect each section’s own specific visual identity; • Develop a design suite of coordinated physical elements, materials, finishes and colours that are compatible with the surrounding landscape context; • Ensure physical design elements and objects relate to one another and the scale of their setting; • Ensure amenity areas co-locate a set of facilities (such as toilets and seats and shelters), interpretive information, and signage; • Consider the placement of emergency collection points (e.g. by helicopter or vehicle) and identify these for users and emergency services; and • Ensure design elements are simple, timeless, easily replicated, and minimise visual clutter. The design of signage and furniture should be standardised and installed as a consistent design suite across the Trail network. Small design modifications and tweaks can be made to the suite for each Section using unique graphics on signage, different colours, patterns and motifs that identifies the unique character for individual Sections along the Trail. -
Introduction to the District
Hauraki District Plan September 2014 6.2 INDIGENOUS BIODIVERSITY AND SIGNIFICANT NATURAL AREAS 6.2.1 BACKGROUND (1) PART 2 RESOURCE MANAGEMENT ACT 1991 (RMA) (a) The RMA has a key role in managing our indigenous biological diversity. Almost all forms of resource use affect indigenous biodiversity, and biodiversity is recognised in the Act in many ways. Part 2 of the Act places a responsibility on the Council to recognise and provide for the general protection of indigenous vegetation and habitats of indigenous fauna. (b) Section 5(2)(b) of the Act refers to safeguarding the life-supporting capacity of ecosystems. Section 6(c) places a responsibility on Council to protect areas of significant indigenous vegetation and significant habitats of indigenous fauna as a matter of “national importance”. Section 7 also requires Council to have particular regard to the maintenance and enhancement of amenity values (Section 7(c)) and the intrinsic value of ecosystems (Section 7(d)). The definition of “Intrinsic Values” in the Act includes values derived from biological and genetic diversity and the essential characteristics that determine an ecosystem’s integrity, form, functioning and resilience. These characteristics are also integral to the life-supporting capacity of ecosystems identified in Section 5(2)(b). In addition, it is understood that some areas of indigenous biodiversity have cultural values of importance to tangata whenua, and through the protection of indigenous biodiversity for ecosystem reasons, such protection can also assist Council in carrying out its responsibilities under Section 8 of the Act. (c) Section 31 of the Act provides that it is the function of territorial authorities to control the effects of the use of land for the maintenance of indigenous biological diversity. -
Re-Establishing North Island Kākā (Nestor Meridionalis Septentrionalis
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. Re-establishing North Island kākā (Nestor meridionalis septentrionalis) in New Zealand A thesis presented in fulfilment of the requirements for the degree of Master of Science In Conservation Biology Massey University Auckland, New Zealand Tineke Joustra 2018 ii For Orlando, Aurora and Nayeli “I don’t want my children to follow in my footsteps, I want them to take the path next to me and go further than I could have ever dreamt possible” Anonymous iii iv Abstract Recently there has been a global increase in concern over the unprecedented loss of biodiversity and how the sixth mass extinction event is mainly due to human activities. Countries such as New Zealand have unique ecosystems which led to the evolution of many endemic species. One such New Zealand species is the kākā (Nestor meridionalis). Historically, kākā abundance has been affected by human activities (kākā were an important food source for Māori and Europeans). Today, introduced mammalian predators are one of the main threats to wild kākā populations. Although widespread and common throughout New Zealand until the 1800’s, kākā populations on the mainland now heavily rely on active conservation management. The main methods of kākā management include pest control and re-establishments. This thesis evaluated current and past commitments to New Zealand species restoration, as well as an analysis of global Psittacine re-establishment efforts. -
(Strigops Habroptilus) on Maud Island
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Lincoln University Research Archive 143 Seasonal changes in home range size and habitat selection by kakapo (Strigops habroptilus) on Maud Island JULIE WALSH Abstract Seasonal changes in home range size and habitat selection of kakapo Ecology and Entomology Group, P.O. Box 84, (Strigops habroptilus) were investigated on Maud Island. Kakapo were radio-tracked Lincoln University, New Zealand. at night in each of the four seasons between December 2000 and October 2001. [email protected] Home ranges were estimated for four adult males, three juvenile males and two juvenile females in each season and for nine females in summer, each based on KERRY-JAYNE WILSON 20 radio-fixes per season. Home range size varied from 1.8 to 145.0 ha using the Bio-Protection and Ecology Division, P.O. minimum convex polygon method. Home ranges were smallest in winter. Habitat Box 84, Lincoln University, New Zealand selection was determined by overlaying the kakapo locations and home ranges on a vegetation map of the island. For each season selection ratios were calculated GRAEME P. ELLIOTT for each vegetation community. Pine plantation (Pinus radiata) was selected for in Research, Development & Improvement summer, whereas the treeland community dominated by five- fingerPseudopanax ( Division, Department of Conservation, arbereus) was selected for in the autumn. Dense pole stands of manuka Private Bag 5, Nelson, New Zealand (Leptospemum scoparium) and pasture communities were avoided by kakapo. Walsh, J.; Wilson, K-J.; Elliott, G.P. 2006. Seasonal changes in home range size and habitat selection by kakapo (Strigops habroptilus) on Maud Island. -
Abundance and Future Options for Wetapunga on Little Barrier Island
Abundance and future options for wetapunga on Little Barrier Island SCIENCE FOR CONSERVATION: 48 George Gibbs and Mary McIntyre Published by Department of Conservation P.O. Box 10-420 Wellington, New Zealand 1 Science for Conservation presents the results of investigations contracted to science providers outside the Department of Conservation. Reports are subject to peer review within and outside the Department. May 1997, Department of Conservation ISSN 1173-2946 ISBN 0-478-01896-7 This publication originated from work done under Department of Conservation contract 1959 carried out by George Gibbs and Mary McIntyre, School of Biological Sciences, Victoria University, PO Box 600, Wellington. It was approved for publication by the Director, Science and Research Division, Department of Conservation, Wellington. Cataloguing-in-Publication data Gibbs, George W. (George William), 1937– Abundance and future options for wetapunga on Little Barrier Island / George Gibbs and Mary McIntyre. Wellington, N.Z. : Dept. of Conservation, 1997. 1 v. ; 30 cm. (Science for conservation, 1173-2946 ; 48.) Includes bibliographical references. ISBN 0478018967 1. Giant wetas- -New Zealand- -Little Barrier Island. 2. Weta punga. I. McIntyre, M. E. (Mary E.) II. Title. III. Series: Science for conservation (Wellington, N.Z.) ; 48. 595.7260993245 20 zbn97-045241 2 CONTENTS Abstract 5 1. Introduction 5 1.1 Objectives 6 1.2 Visits to Little Barrier Island 6 2. Assessment of numbers 6 2.1 Methods 7 2.2 Results 8 2.3 Discussion of population size 8 3. Habitat use 9 3.1 Use of shelters 10 3.2 Radiotracking study 10 3.3 Discussion of predators and role of shelters 12 4. -
PETITION To: KEN SALAZAR, SECRETARY, US DEPARTMENT
PETITION To: KEN SALAZAR, SECRETARY, U.S. DEPARTMENT OF THE INTERIOR Petition: To List All Live Amphibians in Trade as Injurious Unless Free of Batrachochytrium dendrobatidis Submitted by: Defenders of Wildlife, 1130 17th Street NW, Washington, DC 20036 Date: September 9, 2009 Executive Summary and Text of Proposed Amendment: Robust measures to conserve Earth’s amphibians are urgently needed. The absence of Federal protective measures applied to the import, interstate commerce and export of live amphibians has led to excessive risk that the globally devastating Batrachochytrium dendrobatidis (“Bd”) pathogen, which causes the deadly disease chytridiomycosis, will continue to enter, spread within and be shipped out of the United States. This shockingly unregulated trade - primarily for pet use and as live animals for consumption as frog legs - continues to threaten the survival of multiple amphibians, including, but not limited to, U.S. and foreign species listed by the U.S. Fish and Wildlife Service (FWS) under the Endangered Species Act (ESA), candidate species and other species as well. All Federal agencies have affirmative duties to protect these species. However, the only Federal regulation on the amphibian trade, 50 CFR §16.14, now allows “all species” of amphibians to be “imported, transported and possessed” without restriction. This FWS regulation is far too liberal and should be amended to require health certification and handling based on a consensus international standard, adopted by the World Organization for Animal Health (OIE), which the United States voted to support at the May 2008 annual meeting of the parties.. The U.S. vote in support of the OIE standard came from the U.S. -
Chapter 10. Amphibians of the Palaearctic Realm
CHAPTER 10. AMPHIBIANS OF THE PALAEARCTIC REALM Figure 1. Summary of Red List categories Brandon Anthony, J.W. Arntzen, Sherif Baha El Din, Wolfgang Böhme, Dan Palaearctic Realm contains 6% of all globally threatened amphibians. The Palaearctic accounts for amphibians in the Palaearctic Realm. CogĄlniceanu, Jelka Crnobrnja-Isailovic, Pierre-André Crochet, Claudia Corti, for only 3% of CR species and 5% of the EN species, but 9% of the VU species. Hence, on the The percentage of species in each category Richard Griffiths, Yoshio Kaneko, Sergei Kuzmin, Michael Wai Neng Lau, basis of current knowledge, threatened Palaearctic amphibians are more likely to be in a lower is also given. Pipeng Li, Petros Lymberakis, Rafael Marquez, Theodore Papenfuss, Juan category of threat, when compared with the global distribution of threatened species amongst Manuel Pleguezuelos, Nasrullah Rastegar, Benedikt Schmidt, Tahar Slimani, categories. The percentage of DD species, 13% (62 species), is also much less than the global Max Sparreboom, ùsmail Uøurtaû, Yehudah Werner and Feng Xie average of 23%, which is not surprising given that parts of the region have been well surveyed. Red List Category Number of species Nevertheless, the percentage of DD species is much higher than in the Nearctic. Extinct (EX) 2 Two of the world’s 34 documented amphibian extinctions have occurred in this region: the Extinct in the Wild (EW) 0 THE GEOGRAPHIC AND HUMAN CONTEXT Hula Painted Frog Discoglossus nigriventer from Israel and the Yunnan Lake Newt Cynops Critically Endangered (CR) 13 wolterstorffi from around Kunming Lake in Yunnan Province, China. In addition, one Critically Endangered (EN) 40 The Palaearctic Realm includes northern Africa, all of Europe, and much of Asia, excluding Endangered species in the Palaearctic Realm is considered possibly extinct, Scutiger macu- Vulnerable (VU) 58 the southern extremities of the Arabian Peninsula, the Indian Subcontinent (south of the latus from central China. -
Breeding Petrels of Dusky Sound, Fiordland – Survivors from a Century of Stoat Invasions
136 Notornis, 2017, Vol. 64: 136-153 0029-4470 © The Ornithological Society of New Zealand Inc. Breeding petrels of Dusky Sound, Fiordland – survivors from a century of stoat invasions COLIN M. MISKELLY* ALAN J.D. TENNYSON JEAN-CLAUDE STAHL Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington 6140, New Zealand ANDREW F. SMART HANNAH K. EDMONDS PETER G. MCMURTRIE Department of Conservation, PO Box 29, Te Anau 9600, New Zealand Abstract A total of 49 breeding colonies of 3 petrel species was found on 44 of 56 islands surveyed in Dusky Sound, Fiordland National Park, New Zealand, in November 2016. Sooty shearwater (Puffinus griseus) was the most widespread and abundant species, with an estimated 21,400 burrows on 35 islands. Mottled petrels (Pterodroma inexpectata) were breeding on 12 islands (5500 burrows estimated), and broad-billed prions (Pachyptila vittata) on 2 islands (560 burrows estimated). Sooty shearwaters were found breeding among mottled petrels on 4 islands, and among broad-billed prions on 1 island. This is a 5-fold increase in the number of petrel colonies in Dusky Sound identified in published accounts, and the first estimate of the number of burrows on each island. Long-term survival of most or all of these colonies is dependent on ongoing control of stoats (Mustela erminea) in Dusky Sound. However, we suggest that islands too small to support a resident stoat population provided partial refugia for petrels, even if the islands are within stoat swimming range, allowing petrels to persist for multiple generations. In contrast, petrels were apparently rapidly extirpated from islands over 100 ha, where stoats maintained a resident population. -
3Systematics and Diversity of Extant Amphibians
Systematics and Diversity of 3 Extant Amphibians he three extant lissamphibian lineages (hereafter amples of classic systematics papers. We present widely referred to by the more common term amphibians) used common names of groups in addition to scientifi c Tare descendants of a common ancestor that lived names, noting also that herpetologists colloquially refer during (or soon after) the Late Carboniferous. Since the to most clades by their scientifi c name (e.g., ranids, am- three lineages diverged, each has evolved unique fea- bystomatids, typhlonectids). tures that defi ne the group; however, salamanders, frogs, A total of 7,303 species of amphibians are recognized and caecelians also share many traits that are evidence and new species—primarily tropical frogs and salaman- of their common ancestry. Two of the most defi nitive of ders—continue to be described. Frogs are far more di- these traits are: verse than salamanders and caecelians combined; more than 6,400 (~88%) of extant amphibian species are frogs, 1. Nearly all amphibians have complex life histories. almost 25% of which have been described in the past Most species undergo metamorphosis from an 15 years. Salamanders comprise more than 660 species, aquatic larva to a terrestrial adult, and even spe- and there are 200 species of caecilians. Amphibian diver- cies that lay terrestrial eggs require moist nest sity is not evenly distributed within families. For example, sites to prevent desiccation. Thus, regardless of more than 65% of extant salamanders are in the family the habitat of the adult, all species of amphibians Plethodontidae, and more than 50% of all frogs are in just are fundamentally tied to water. -
Native Frog (Leiopelma Spp.) Recovery Plan, 2013–2018
THREATENED SPECIES RECOVERY PLAN 63 Native frog (Leiopelma spp.) recovery plan, 2013–2018 Phillip J. Bishop, Lisa A. Daglish, Amanda J.M. Haigh, Leigh J. Marshall, Mandy D. Tocher and Kate L. McKenzie Cover: Archey’s frog (Leiopelma archeyi) on kiwikiwi (Blechnum fluviatile). Photo: Kate McKenzie. This report is available from the departmental website in pdf form. Titles are listed in our catalogue on the website, refer www.doc.govt.nz under Publications, then Science & technical. © Copyright December 2013, New Zealand Department of Conservation ISSN 1178–0169 (web PDF) ISBN 978–0–478–15007–0 (hardcopy) 978–0–478–15008–7 (web PDF) This report was prepared for publication by the Publishing Team; editing and layout by Amanda Todd. Publication was approved by the Deputy Director-General, Science and Capability Group, Department of Conservation, Wellington, New Zealand. Published by Publishing Team, Department of Conservation, PO Box 10420, The Terrace, Wellington 6143, New Zealand. In the interest of forest conservation, we support paperless electronic publishing. Foreword The former Waikato Conservator of the Department of Conservation (DOC) formally approved this threatened species recovery plan in 2013. A review of the plan is due in 2017, or sooner if new information or technology leads to a significant change in management direction. This plan will remain operative until a new plan has been prepared and approved, or will become redundant if recovery is achieved and management effort enters a ‘maintenance phase’. The Native Frog Recovery Group prepared this plan in conjunction with people interested in or affected by this plan, or with an expert knowledge of these species. -
Complete Nucleotide Sequence and Gene Rearrangement of the Mitochondrial Genome of the Bell-Ring Frog, Buergeria Buergeri (Family Rhacophoridae)
Genes Genet. Syst. (2004) 79, p. 151–163 Complete nucleotide sequence and gene rearrangement of the mitochondrial genome of the bell-ring frog, Buergeria buergeri (family Rhacophoridae) Naomi Sano1, Atsushi Kurabayashi1, Tamotsu Fujii2, Hiromichi Yonekawa3, and Masayuki Sumida1* 1Institute for Amphibian Biology, Hiroshima University, Higashihiroshima, Hiroshima 739-8526, Japan 2Department of Health Science, Hiroshima Prefectural Women’s University, Hiroshima 734-8558, Japan 3Department of Laboratory Animal Science, The Tokyo Metropolitan Institute of Medical Science, Tokyo 113-8613, Japan (Received 22 March 2004, accepted 26 May 2004) In this study we determined the complete nucleotide sequence (19,959 bp) of the mitochondrial DNA of the rhacophorid frog Buergeria buergeri. The gene content, nucleotide composition, and codon usage of B. buergeri conformed to those of typ- ical vertebrate patterns. However, due to an accumulation of lengthy repetitive sequences in the D-loop region, this species possesses the largest mitochondrial genome among all the vertebrates examined so far. Comparison of the gene organ- izations among amphibian species (Rana, Xenopus, salamanders and caecilians) revealed that the positioning of four tRNA genes and the ND5 gene in the mtDNA of B. buergeri diverged from the common vertebrate gene arrangement shared by Xenopus, salamanders and caecilians. The unique positions of the tRNA genes in B. buergeri are shared by ranid frogs, indicating that the rearrangements of the tRNA genes occurred in a common ancestral lineage of ranids and rhacophorids. On the other hand, the novel position of the ND5 gene seems to have arisen in a lineage leading to rhacophorids (and other closely related taxa) after ranid divergence.