Te Kakahu Skink – Anchor Population
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On Ulva Island
Abundance and dispersal of translocated common skink (Oligosoma polychroma) on Ulva Island Helen Sharpe A report submitted in partial fulfilment of the Post-graduate Diploma in Wildlife Management University of Otago 2011 University of Otago Department of Zoology P.O. Box 56, Dunedin New Zealand WLM Report Number: 250 Abundance and dispersal of translocated common skink (Oligosoma polychroma) on Ulva Island A report prepared for the Department of Conservation in association with Otago University’s Diploma of Wildlife Management. Helen Sharpe July 2011 2 Abundance and dispersal of translocated common skink (Oligosoma polychroma) on Ulva Island Contents Summary 2 Introduction 3 Methods 4 Results 8 Discussion 9 Recommendations 13 Acknowledgements 15 References 16 Figures and tables 18 3 Abundance and dispersal of translocated common skink (Oligosoma polychroma) on Ulva Island Summary This report describes a monitoring study carried out in 2011 to investigate the abundance and distribution of common skink (Oligosoma polychroma) on Ulva Island, Southland, New Zealand. Common skinks were introduced to Ulva in 2005 and 2006 for ecosystem restoration, and to investigate effects of weka (Gallirallus australis scotti) predation. Skinks were monitored over 3 non-consecutive days using artificial cover objects. Where possible skinks were caught, weighed, measured and photographed. A total of 18 sightings were made which indicates a substantial drop in both populations but especially at West End Beach. A combination of insufficient habitat and predation/competition by weka are the probable causes. However some uncertainties with monitoring are acknowledged, with regard to sub-optimal weather conditions and ‘settling’ time for new ACOS. Skinks appear not to have dispersed more than 20-30 metres from their release site. -
Reptiles and Amphibians of Otago
Society for Research on Amphibians and Reptiles in New Zealand (SRARNZ) presents Reptiles and Amphibians of Otago Otago is a large (31,251 km2) and lightly populated region of the southern South Island of Aotearoa New Zealand, stretching from the eastern coastline west to the Southern Alps. The earliest humans, of East Polynesian origin, arrived about 700 years ago. The largest settlement today is the coastal city of Dunedin (pop. >127,000), which grew from a Scottish influx in the 1800s. The Otago Regional Council administers the region, and tribal authority (mana whenua) rests with the iwi of Ngāi Tahu. Climates in the Otago region (roughly 45°– leiopelmatid frogs survive elsewhere in 47°S) range from changeable, cool- New Zealand. Two species of introduced temperate conditions near the coast to frogs are present, but there are no the near-continental climates (baking hot crocodilians, salamanders, terrestrial summers, freezing winters) of the interior. snakes or turtles. Marine turtles (mainly The region provides varied habitats for leatherback turtles, Dermochelys coriacea) herp species, including sand-dunes, visit the coastal waters of Otago but do grasslands, shrublands, wetlands, forests, not nest here. rock structures and scree slopes, some occupied to at least 1900 m above sea level. Today’s herpetofauna is dominated by lizards (solely geckos and skinks), including about 10 described species. A further 12 or more undescribed taxa are recognised Otago by tag names for conservation purposes, and we follow that approach here. All lizards in Otago are viviparous and long- lived, and remain vulnerable to ongoing habitat loss and predation by introduced mammals. -
Ecology of Scree Skinks (Oligosoma Waimatense) in O Tu Wharekai Wetland, Mid-Canterbury High Country, New Zealand
Lettink,New Zealand Monks: Journal Scree ofskink Ecology ecology (2019) 43(1): 3354 © 2018 New Zealand Ecological Society. RESEARCH Ecology of scree skinks (Oligosoma waimatense) in O Tu Wharekai Wetland, mid-Canterbury high country, New Zealand Marieke Lettink1* and Joanne M. Monks2 1Fauna Finders, 45 Park Terrace, Corsair Bay, Christchurch 8082 2Department of Conservation, Ōtepoti/Dunedin Office, PO Box 5244, Dunedin 9058 *Author for correspondence (Email: [email protected]) Published online: 17 October 2018 Abstract: Many of New Zealand’s 104 lizard taxa are restricted to the country’s main islands where they are vulnerable to a range of threats. Information on population trends and basic ecological data are lacking for most species, hampering conservation efforts. We monitored a population of scree skinks (Oligosoma waimatense; conservation status: Nationally Vulnerable) in an alluvial stream bed in O Tu Wharekai Wetland in the mid- Canterbury high country over 10 years (2008−2018) to understand aspects of the population’s ecology, and to clarify potential threats and options for management. Although there was no linear trend in scree skink capture numbers over this time, an 84% decline was observed following severe and unseasonal flooding in May 2009. Capture numbers recovered over c. 8.5 years in the absence of any species management. Skinks ranged in size from 60−114 mm (snout-to-vent length). Home range size estimates varied from 39.5 to 950 m2 (100% Minimum Convex Polygons) and their mean size was smaller than those reported for closely-related species. Photo-identification was not sufficiently accurate for long-term individual identification. -
Conserviing Fiordland's Biodiversity 1987-2015 Part 3
Ecosystem response to pest control Flora and plant communities • Recognition and documentation of the flora, vegetation and wider ecological values of the Since 1987, considerable effort – both planned and Fiordland / Te Anau Basin area. opportunistic – has gone into surveying threatened • Identification of national strongholds for heart-leaved flora (plant species) and vegetation in general (plant kōhūhū, the shrub Melicytus flexuosus, the tree daisy communities) in Fiordland. This region is not only Olearia lineata and small-leaved coprosma in Back floristically significant nationally, but is also an important Valley. stronghold for several threatened species. • Recognition that the lakeshore turfs found around 11 Around 1000 vascular plant taxa are thought to occur Lakes Manapouri and Te Anau are among the in Fiordland, which makes the region much richer, most significant plant habitats in Fiordland (these ecologically, than previously understood. The Fiord communities are a national stronghold for several Ecological Region contains 11 species classified (under plant species). the New Zealand Threat Classification System) as • Protection of the Dale bog pine area as Dale Threatened, 96 as At Risk, 2 as Vagrant and 5 as Data Conservation Area. Deficient – and several of these have their national stronghold within Fiordland. Nationally important • Retirement of the Mavora Lakes and Eglinton Valley populations of some species classified as Naturally from grazing. Uncommon also occur. Fiordland is also known to be an • Working with community groups to restore and important region for endemism, with 24 taxa endemic manage important ecological values (notably to Fiordland, 11 near-endemic and a further 13 restricted Pomona Island Charitable Trust, Te Puka-Hereka/ to southern New Zealand. -
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. -
Assisted Breeding of Skinks Or How to Teach a Lizard Old Tricks!
Herpetological Conservation and Biology 5(2):311-319. Symposium: Reptile Reproduction ASSISTED BREEDING OF SKINKS OR HOW TO TEACH A LIZARD OLD TRICKS! 1 2,3 4 5 FRANK C. MOLINIA , TRENT BELL , GRANT NORBURY , ALISON CREE 1 AND DIANNE M. GLEESON 1Landcare Research, Private Bag 92170, Auckland 1142, New Zealand,e-mail: [email protected] 2Landcare Research, Private Bag 1930, Dunedin 9054, New Zealand 3Current Contact Details: EcoGecko Consultants, e-mail: [email protected] 4Landcare Research, PO Box 282, Alexandra 9340, New Zealand 5Department of Zoology, University of Otago, PO Box 56, Dunedin 9054, New Zealand Abstract.—Reproductive technologies are invaluable tools for understanding how different species reproduce. Contemporary techniques like artificial insemination established long ago in livestock have been used to assist the breeding of threatened species ex situ, even restoring them to nature. Key to successfully adapting these technologies, often to few numbers of endangered animals, is initial testing and development of procedures in a taxonomically related model species. McCann’s Skink (Oligosoma maccanni) is a viviparous lizard that is still relatively abundant and its reproductive cycle in the subalpine area of Macraes Flat in southern New Zealand has recently been described. Assisted breeding techniques are being developed in this skink as a model for threatened lizard species, such as the Grand Skink (Oligosoma grande) and Otago Skink (Oligosoma otagense). Progress on methods to collect, assess and store sperm, and artificial insemination are reported here. These techniques will need refinement to be effectively adapted to threatened lizards but will significantly increase our knowledge of their unique reproductive mechanisms. -
Oligosoma Ornatum; Reptilia: Scincidae) Species Complex from Northern New Zealand
Zootaxa 3736 (1): 054–068 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3736.1.2 http://zoobank.org/urn:lsid:zoobank.org:pub:B7D72CD9-BE5D-4603-8BC0-C9FA557C7BEE Taxonomic revision of the ornate skink (Oligosoma ornatum; Reptilia: Scincidae) species complex from northern New Zealand GEOFF B. PATTERSON1,5, ROD A. HITCHMOUGH2 & DAVID G. CHAPPLE3,4 1149 Mairangi Road, Wilton, Wellington, New Zealand 2Department of Conservation, Terrestrial Conservation Unit, PO Box 10-420, Wellington 6143, New Zealand 3School of Biological Sciences, Monash University, Clayton Victoria 3800, Australia 4Allan Wilson Centre for Molecular Ecology and Evolution, School of Biological Sciences, Victoria University of Wellington, P.O. Box 600, Wellington 6140, New Zealand 5Corresponding author. E-mail: [email protected] Abstract Although the New Zealand skink fauna is known to be highly diverse, a substantial proportion of the recognised species remain undescribed. We completed a taxonomic revision of the ornate skink (Oligosoma ornatum (Gray, 1843)) as a pre- vious molecular study indicated that it represented a species complex. As part of this work we have resolved some nomen- clatural issues involving this species and a similar species, O. aeneum (Girard, 1857). A new skink species, Oligosoma roimata sp. nov., is described from the Poor Knights Islands, off the northeast coast of the North Island of New Zealand. This species is diagnosed by a range of morphological characters and genetic differentiation from O. ornatum. The con- servation status of the new taxon appears to be of concern as it is endemic to the Poor Knights Islands and has rarely been seen over the past two decades. -
Whakamana Te Waituna Biodiversity Plan
WHAKAMANA TE WAITUNA BIODIVERSITY PLAN R4701 WHAKAMANA TE WAITUNA BIODIVERSITY PLAN Wire rush rushland amongst mānuka shrubland, near Waituna Lagoon Road. Contract Report No. 4701 February 2019 Project Team: Kelvin Lloyd - Project management Nick Goldwater - Report author Carey Knox - Report author Helen McCaughan - Report author Steve Rate - Report author Fiona Wilcox - Report author Prepared for: Whakamana te Waituna Charitable Trust DUNEDIN OFFICE: 764 CUMBERLAND STREET, DUNEDIN 9016 Ph 03-477-2096, 03-477-2095 HEAD OFFICE: 99 SALA STREET, P.O. BOX 7137, TE NGAE, ROTORUA Ph 07-343-9017; Fax 07-343-9018, email [email protected], www.wildlands.co.nz CONTENTS 1. INTRODUCTION 1 2. PROJECT OBJECTIVE 3 3. PROJECT SCOPE 3 4. METHODS 3 5. CULTURAL CONTEXT 4 6. ECOLOGICAL CONTEXT 5 6.1 Waituna Ecological District 5 6.2 Waterways 5 6.3 Protected Natural Areas 7 6.4 Unprotected natural areas 8 6.5 Threatened land environments 8 6.6 Vegetation and habitats 10 6.7 Overview 10 6.8 Wetland vegetation 10 6.9 Terrestrial vegetation 12 6.10 Other vegetation/habitat types 12 6.11 Naturally uncommon ecosystem types 15 7. FLORA 16 7.1 Indigenous species 16 8. FAUNA 18 8.1 Overview 18 8.2 Birds 18 8.3 Lizards 20 8.4 Aquatic fauna 23 8.5 Terrestrial invertebrates 26 9. THREATS TO ECOLOGICAL VALUES 27 9.1 Overview 27 9.2 Land-based activities 27 9.2.1 Excessive catchment inputs of sediment, nutrients, and pathogens 27 9.2.2 Indigenous vegetation clearance 27 9.2.3 Hydrological modification 27 9.2.4 Stock 28 9.2.5 Other adverse activities 28 9.3 Natural phenomena 28 9.3.1 Fire 28 9.3.2 Sea level rise 29 9.4 Effects at landscape scale 29 9.5 Pest animals and plants 29 9.5.1 Pest animals 29 9.5.2 Pest plants 30 © 2019 Contract Report No. -
Fauna of Australia 2A
FAUNA of AUSTRALIA 26. BIOGEOGRAPHY AND PHYLOGENY OF THE SQUAMATA Mark N. Hutchinson & Stephen C. Donnellan 26. BIOGEOGRAPHY AND PHYLOGENY OF THE SQUAMATA This review summarises the current hypotheses of the origin, antiquity and history of the order Squamata, the dominant living reptile group which comprises the lizards, snakes and worm-lizards. The primary concern here is with the broad relationships and origins of the major taxa rather than with local distributional or phylogenetic patterns within Australia. In our review of the phylogenetic hypotheses, where possible we refer principally to data sets that have been analysed by cladistic methods. Analyses based on anatomical morphological data sets are integrated with the results of karyotypic and biochemical data sets. A persistent theme of this chapter is that for most families there are few cladistically analysed morphological data, and karyotypic or biochemical data sets are limited or unavailable. Biogeographic study, especially historical biogeography, cannot proceed unless both phylogenetic data are available for the taxa and geological data are available for the physical environment. Again, the reader will find that geological data are very uncertain regarding the degree and timing of the isolation of the Australian continent from Asia and Antarctica. In most cases, therefore, conclusions should be regarded very cautiously. The number of squamate families in Australia is low. Five of approximately fifteen lizard families and five or six of eleven snake families occur in the region; amphisbaenians are absent. Opinions vary concerning the actual number of families recognised in the Australian fauna, depending on whether the Pygopodidae are regarded as distinct from the Gekkonidae, and whether sea snakes, Hydrophiidae and Laticaudidae, are recognised as separate from the Elapidae. -
ASH Newsletter 47 E.Pub
THE AUSTRALIAN SOCIETY OF HERPETOLOGISTS INCORPORATED NEWSLETTER 47 2 History of Office Bearers Formation Committee (April 1964):- MJ Littlejohn (Convenor); State Reps IR Straughan (Qld), FJ Mitch- ell (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 Strau- ghan, Editor AK Lee. PRESIDENT:- MJ Littlejohn (1965-69); AK Lee (1969-70); HG Cogger (1971-73); J de Bavay (1974); H Heatwole (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 (2009-2010); L Schwarzkopf (2010-2011); F Lemckert (2011-) VICE-PRESIDENT:- NG Stephenson (1965-67); RE Barwick (1967-69); HG Cogger (1969-70); MJ Lit- tlejohn (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 Thompson (2009-2010); M Hutchinson (2010-); L Schwarzkopf (2010-2011) SECRETARY/TREASURER:- AA Martin (1965-67); GF Watson (1967-72); LA Moffatt (1973-75); J Caughley (19375-76); RWG Jenkins (1976-77); M Davies (1978-83); G Courtice (1983-87); J Wombey (1987-99); S Keogh (1999-2003); N Mitchell (2004-5); E. -
Stoats (Mustela Erminea) Are Primary Predators, Which Are Likely to Be Impacting Significantly on Population Viability
DOI:O’Donnell 10.20417/nzjecol.41.18 et al.: Mammalian predators and alpine fauna 1 REVIEW Impacts of introduced mammalian predators on New Zealand’s alpine fauna Colin F. J. O’Donnell1, Kerry A. Weston1* and Joanne M. Monks2 1Science and Policy Group, Department of Conservation, Private Bag 4715, Christchurch Mail Centre, Christchurch 8140, New Zealand 2Science and Policy Group, Department of Conservation, PO Box 5244, Dunedin 9058, New Zealand *Author for correspondence (Email: [email protected]) Published online: 9 December 2016 Abstract: Alpine zones are threatened globally by invasive species, hunting, and habitat loss caused by fire, anthropogenic development and climate change. These global threats are pertinent in New Zealand, with the least understood pressure being the potential impacts of introduced mammalian predators, the focus of this review. In New Zealand, alpine zones include an extensive suite of cold climate ecosystems covering c. 11% of the land mass. They support rich communities of indigenous invertebrates, lizards, fish, and birds. Many taxa are obligate alpine dwellers, though there is uncertainty about the extent to which distributions of some species are relicts of wider historical ranges. The impacts of introduced mammalian predators are well described in many New Zealand ecosystems, though little is known about the impacts of these predators on alpine fauna. Here we review the importance of alpine habitats for indigenous fauna and the impacts of introduced mammalian predators; and develop a conceptual model explaining threat interactions. Most evidence for predation is anecdotal or comes from studies of species with wider ranges and at lower altitudes. Nevertheless, at least ten introduced predator species have been confirmed as frequent predators of native alpine species, particularly among birds and invertebrates. -
New Zealand Threat Classification System (NZTCS)
NEW ZEALAND THREAT CLASSIFICATION SERIES 17 Conservation status of New Zealand reptiles, 2015 Rod Hitchmough, Ben Barr, Marieke Lettink, Jo Monks, James Reardon, Mandy Tocher, Dylan van Winkel and Jeremy Rolfe Each NZTCS report forms part of a 5-yearly cycle of assessments, with most groups assessed once per cycle. This report is the first of the 2015–2020 cycle. Cover: Cobble skink, Oligosoma aff.infrapunctatum “cobble”. Photo: Tony Jewell. New Zealand Threat Classification Series is a scientific monograph series presenting publications related to the New Zealand Threat Classification System (NZTCS). Most will be lists providing NZTCS status of members of a plant or animal group (e.g. algae, birds, spiders). There are currently 23 groups, each assessed once every 3 years. After each three-year cycle there will be a report analysing and summarising trends across all groups for that listing cycle. From time to time the manual that defines the categories, criteria and process for the NZTCS will be reviewed. Publications in this series are considered part of the formal international scientific literature. 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 Series. © Copyright December 2016, New Zealand Department of Conservation ISSN 2324–1713 (web PDF) ISBN 978–1–98–851400–0 (web PDF) This report was prepared for publication by the Publishing Team; editing and layout by Lynette Clelland. Publication was approved by the Director, Terrestrial Ecosystems Unit, Department of Conservation, Wellington, New Zealand. Published by Publishing Team, Department of Conservation, PO Box 10420, The Terrace, Wellington 6143, New Zealand.