Recent Developments in New Zealand Herpetofauna Research
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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. -
Report Format WITHOUT PHOTOS
LIZARD MANAGEMENT PLAN WAKANUI CREEK REALIGNMENT 28 FEBRUARY 2018 LIZARD MANAGEMENT PLAN WAKANUI CREEK REALIGNMENT PREPARED BY: DYLAN VAN WINKEL BIORESEARCHES GROUP LTD 68 BEACH ROAD, AUCKLAND [email protected] FOR: AECOM NEW ZEALAND LIMITED PO BOX 4241 SHORTLAND ST AUCKLAND 1140 DATE: 28 FEBRUARY 2018 REFERENCE: BIORESEARCHES (2017). LIZARD MANAGEMENT PLAN: WAKANUI CREEK REALIGNMENT COVER ILLUSTRATION: OLIGOSOMA AFF. POLYCHROMA Level 4, 68 Beach Road, Auckland 1010; PO Box 2727, Shortland Street, Auckland 1140. T: (09) 379-9417; www.bioresearches.co.nz CONTENTS Page 1 INTRODUCTION ................................................................................................................ 1 2 LIZARD MANAGEMENT PLAN ........................................................................................... 2 2.1 Context of the lizard management plan .............................................................. 2 2.2 Project area and area of affected habitat ........................................................... 2 2.3 Local lizard populations ....................................................................................... 5 2.4 Management of resident lizards .......................................................................... 5 3 LIZARD SALVAGE AND RELOCATION ................................................................................. 6 3.1 Lizard capture ...................................................................................................... 6 3.1.1 Active Searches ....................................................................................... -
Cryptic Extinction of a Common Pacific Lizard Emoia Impar (Squamata, Scincidae) from the Hawaiian Islands
Cryptic extinction of a common Pacific lizard Emoia impar (Squamata, Scincidae) from the Hawaiian Islands R OBERT F ISHER and I VAN I NEICH Abstract Most documented declines of tropical reptiles are Introduction of dramatic or enigmatic species. Declines of widespread species tend to be cryptic. The early (1900s) decline and xtinctions on islands are rampant and have many extinction of the common Pacific skink Emoia impar from Ecauses. For reptiles, particularly lizards, insular extinc- the Hawaiian Islands is documented here through an tions greatly exceed those of mainland species and the assessment of literature, museum vouchers and recent extinction of smaller lizard species is rarely documented 1991 fieldwork. This decline appears contemporaneous with the (Case et al., ). Incomplete knowledge of island fauna documented declines of invertebrates and birds across the hinders an understanding of the true loss of diversity from Hawaiian Islands. A review of the plausible causal factors these ecosystems, and the issue of morphologically cryptic fi indicates that the spread of the introduced big-headed ant species also masks quanti cation of these extirpations or 2007 fi Pheidole megacephala is the most likely factor in this lizard extinctions (Bickford et al., ). The Paci c Basin ’ decline. The introduction and spread of a similar skink contains the majority of the world s tropical islands. These Lampropholis delicata across the islands appears to are most often inhabited by lizards of the families Scincidae 1995 1996 temporally follow the decline of E. impar, although there and Gekkonidae (Adler et al., ; Allison, ; Fisher, 1997 is no evidence of competition between these species. -
Environmental Pest Plants
4.8.3 Indigenous forest on the range and plateaus The Kaimai forests were included in the National Forest Survey (NFS) of indigenous timber resources of 1946-55. The southern half of the ranges was systematically sampled in 1946-48 and the northern half sampled less intensively in 1951-52. These data were used for the compilation of forest type maps (Dale and James 1977). The northern ranges were further sampled by the Ecological Forest Survey in 1965-66, to provide data for more detailed ecological typing. Descriptions of vegetation composition and pattern on the range and plateaus are provided by Dale and James (1977), Clarkson (2002), and Burns and Smale (2002). Other vegetation maps are provided by Nicholls (1965, 1966a&b, 1967a&b, 1971a&b, 1974a, 1975). Further descriptive accounts are provided by Nicholls (1968, 1969, 1972, 1976a&b, 1978, 1983a-c, 1984, 1985a&b, 2002). Beadel (2006) provides a comprehensive overview of vegetation in the Otanewainuku Ecological District and also provides vegetation descriptions and vegetation type maps for privately-owned natural areas within the tract, such as at Te Waraiti and the Whaiti Kuranui Block. Humphreys and Tyler (1990) provide similar information for the Te Aroha Ecological District. A broad representation of indigenous forest pattern is provided in Figure 9. Tawa and kamahi (Weinmannia racemosa) with scattered emergent rimu and northern rata dominates forests on the Mamaku Plateau (Nicholls 1966, Smale et al. 1997). Rimu increases in abundance southwards across the plateau, as the contribution of coarse rhyolitic tephra to soils increased (Smale et al. 1997). Beeches (Nothofagus spp.) (beeches) are present locally on the plateau (Nicholls 1966). -
New Zealand’S Sixth National Report to the United Nations Convention on Biological Diversity
New Zealand’s Sixth National Report to the United Nations Convention on Biological Diversity Reporting period: 2014–2018 Cover: View of Palliser Bay, looking west from Mt Surf, Aorangi Mountains, southern North Island, New Zealand. Photo: Joe Hansen. This document may be cited as: Department of Conservation 2019: New Zealand’s Sixth National Report to the United Nations Convention on Biological Diversity. Reporting period: 2014–2018. Department of Conservation, Wellington, New Zealand. Available at: https://www.cbd.int/countries/?country=nz. and https://www.doc.govt.nz/about-us/international-agreements/convention-on-biological-diversity/ ISBN (electronic) 978-1-98-851491-8 ISBN (print) 978-1-98-851492-5 Department of Conservation PO Box 10420 Wellington 6143 New Zealand This work is licensed under the Creative Commons Attribution 4.0 International licence. In essence, you are free to copy, distribute and adapt the work, as long as you attribute the work to the Crown and abide by the other licence terms. To view a copy of this licence, visit creativecommons.org/licenses/by/4.0/. Table of Contents INTRODUCTION TO THE 6TH NATIONAL REPORT ........................................................................................................................ 5 1. PEOPLE’S LIVES ARE ENRICHED THROUGH CONNECTION TO NATURE ................................................................................ 7 I. General information ......................................................................................................................................................... -
Australasian Journal of Herpetology ISSN 1836-5698 (Print)1 Issue 12, 30 April 2012 ISSN 1836-5779 (Online) Australasian Journal of Herpetology
Australasian Journal of Herpetology ISSN 1836-5698 (Print)1 Issue 12, 30 April 2012 ISSN 1836-5779 (Online) Australasian Journal of Herpetology Hoser 2012 - Australasian Journal of Herpetology 9:1-64. Available online at www.herp.net Contents on pageCopyright- 2. Kotabi Publishing - All rights reserved 2 Australasian Journal of Herpetology Issue 12, 30 April 2012 Australasian Journal of Herpetology CONTENTS ISSN 1836-5698 (Print) ISSN 1836-5779 (Online) A New Genus of Coral Snake from Japan (Serpentes:Elapidae). Raymond T. Hoser, 3-5. A revision of the Asian Pitvipers, referred to the genus Cryptelytrops Cope, 1860, with the creation of a new genus Adelynhoserea to accommodate six divergent species (Serpentes:Viperidae:Crotalinae). Raymond T. Hoser, 6-8. A division of the South-east Asian Ratsnake genus Coelognathus (Serpentes: Colubridae). Raymond T. Hoser, 9-11. A new genus of Asian Snail-eating Snake (Serpentes:Pareatidae). Raymond T. Hoser, 10-12-15. The dissolution of the genus Rhadinophis Vogt, 1922 (Sepentes:Colubrinae). Raymond T. Hoser, 16-17. Three new species of Stegonotus from New Guinea (Serpentes: Colubridae). Raymond T. Hoser, 18-22. A new genus and new subgenus of snakes from the South African region (Serpentes: Colubridae). Raymond T. Hoser, 23-25. A division of the African Genus Psammophis Boie, 1825 into 4 genera and four further subgenera (Serpentes: Psammophiinae). Raymond T. Hoser, 26-31. A division of the African Tree Viper genus Atheris Cope, 1860 into four subgenera (Serpentes:Viperidae). Raymond T. Hoser, 32-35. A new Subgenus of Giant Snakes (Anaconda) from South America (Serpentes: Boidae). Raymond T. Hoser, 36-39. -
Impact of Tail Loss on the Behaviour and Locomotor Performance of Two Sympatric Lampropholis Skink Species
Impact of Tail Loss on the Behaviour and Locomotor Performance of Two Sympatric Lampropholis Skink Species Gillian L. Cromie, David G. Chapple* School of Biological Sciences, Monash University, Clayton, Victoria, Australia Abstract Caudal autotomy is an anti-predator behaviour that is used by many lizard species. Although there is an immediate survival benefit, the subsequent absence of the tail may inhibit locomotor performance, alter activity and habitat use, and increase the individuals’ susceptibility to future predation attempts. We used laboratory experiments to examine the impact of tail autotomy on locomotor performance, activity and basking site selection in two lizard species, the delicate skink (Lampropholis delicata) and garden skink (L. guichenoti), that occur sympatrically throughout southeastern Australia and are exposed to an identical suite of potential predators. Post-autotomy tail movement did not differ between the two Lampropholis species, although a positive relationship between the shed tail length and distance moved, but not the duration of movement, was observed. Tail autotomy resulted in a substantial decrease in sprint speed in both species (28– 39%), although this impact was limited to the optimal performance temperature (30uC). Although L. delicata was more active than L. guichenoti, tail autotomy resulted in decreased activity in both species. Sheltered basking sites were preferred over open sites by both Lampropholis species, although this preference was stronger in L. delicata. Caudal autotomy did not alter the basking site preferences of either species. Thus, both Lampropholis species had similar behavioural responses to autotomy. Our study also indicates that the impact of tail loss on locomotor performance may be temperature-dependent and highlights that future studies should be conducted over a broad thermal range. -
NSW REPTILE KEEPERS' LICENCE Species Lists 1006
NSW REPTILE KEEPERS’ LICENCE SPECIES LISTS (2006) The taxonomy in this list follows that used in Wilson, S. and Swan, G. A Complete Guide to Reptiles of Australia, Reed 2003. Common names generally follow the same text, when common names were used, or have otherwise been lifted from other publications. As well as reading this species list, you will also need to read the “NSW Reptile Keepers’ Licence Information Sheet 2006.” That document has important information about the different types of reptile keeper licenses. It also lists the criteria you need to demonstrate before applying to upgrade to a higher class of licence. THESE REPTILES CAN ONLY BE HELD UNDER A REPTILE KEEPERS’ LICENCE OF CLASS 1 OR HIGHER Code Scientific Name Common Name Code Scientific Name Common Name Turtles Monitors E2018 Chelodina canni Cann’s Snake-necked Turtle G2263 Varanus acanthurus Spiney-tailed Monitor C2017 Chelodina longicollis Snake-necked Turtle Q2268 Varanus gilleni Pygmy Mulga Monitor G2019 Chelodina oblonga Oblong Turtle G2271 Varanus gouldii Sand Monitor Y2028 Elseya dentata Northern Snapping Turtle M2282 Varanus tristis Black-Headed Monitor K2029 Elseya latisternum Saw-shelled Turtle Y2776 Elusor macrurus Mary River Turtle E2034 Emydura macquarii Murray Short-necked Turtle Skinks T2031 Emydura macquarii dharra Macleay River Turtle A2464 Acritoscincus platynotum Red-throated Skink T2039 Emydura macquarii dharuk Sydney Basin Turtle W2331 Cryptoblepharus virgatus Cream-striped Wall Skink T2002 Emydura macquarii emmotti Emmott’s Short-necked Turtle W2375 -
Motuora Native Species Restoration Plan
Motuora Native Species Restoration Plan JUNE 2007 Motuora Native Species Restoration Plan By Robin Gardner-Gee, Sharen Graham, Richard Griffiths, Melinda Habgood, Shelley Heiss Dunlop and Helen Lindsay MOTUORA RESTORATION SOCIETY (INC) PO Box 100-132, NSMC, Auckland. Foreward Deciding to write a Restoration Plan for Motuora was a huge undertaking for a voluntary group, especially since most of those whose help we needed already had busy lives. The project required surveys on the island to establish what plants and animals were already there, followed by much discussion and the writing of the various sections. These sections then had to be edited to make a unified whole. This document could not have been written without the enthusiasm, knowledge, and commitment of a group of keen environmentalists who put in long hours to produce the Restoration Plan. The Motuora Restoration Society thanks the many people and organizations who have provided information, advice and comment on this document. Particular thanks to: Robin Gardner-Gee for her invertebrate knowledge Sharen Graham for her bird knowledge Richard Griffiths for pulling the document together to present an overview of the whole island ecology Melinda Habgood for her reptile knowledge Shelley Heiss-Dunlop for her plant knowledge Helen Lindsay for her input into the plant section and for co-ordinating the project especially in the beginning Te Ngahere Native Forest Management for supporting this project Department of Conservation staff for support and encouragement. The Motuora Restoration Society thanks you all for your generosity in sharing your learning and experience. Ray Lowe Chairman Motuora Restoration Society i ii Executive Summary Motuora is an 80 hectare island in the Hauraki Gulf to the south of Kawau Island. -
Phylogeography of the Endangered Otago Skink, Oligosoma Otagense: Population Structure, Hybridisation and Genetic Diversity in Captive Populations
Phylogeography of the Endangered Otago Skink, Oligosoma otagense: Population Structure, Hybridisation and Genetic Diversity in Captive Populations David G. Chapple1,2*, Alisha Birkett3,4, Kimberly A. Miller1, Charles H. Daugherty2, Dianne M. Gleeson3,4 1 School of Biological Sciences, Monash University, Clayton, Victoria, Australia, 2 Allan Wilson Centre for Molecular Ecology and Evolution, School of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand, 3 School of Biological Sciences, University of Auckland, Auckland, New Zealand, 4 Ecological Genetics Laboratory, Landcare Research, Mt. Albert, Auckland, New Zealand Abstract Climatic cooling and substantial tectonic activity since the late Miocene have had a pronounced influence on the evolutionary history of the fauna of New Zealand’s South Island. However, many species have recently experienced dramatic range reductions due to habitat fragmentation and the introduction of mammalian predators and competitors. These anthropogenic impacts have been particularly severe in the tussock grasslands of the Otago region. The Otago skink (Oligosoma otagense), endemic to the region, is one of the most critically endangered vertebrates in New Zealand. We use mitochondrial DNA sequence data to investigate the evolutionary history of the Otago skink, examine its population genetic structure, and assess the level of genetic diversity in the individuals in the captive breeding program. Our data indicate that the Otago skink diverged from its closest relatives in the Miocene, consistent with the commencement of tectonic uplift of the Southern Alps. However, there is evidence for past introgression with the scree skink (O. waimatense) in the northern Otago-southern Canterbury region. The remnant populations in eastern Otago and western Otago are estimated to have diverged in the mid-Pliocene, with no haplotypes shared between these two regions. -
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. -
Husbandry Guidelines for Australian Water Dragon
Husbandry Guidelines for Australian Water Dragon Physignathus lesueurii (Reptilia: Agamidae) Compiler: Chris Hosking Date of Preparation: June 2010 Western Sydney Institute of TAFE, Richmond. Course Name and Number: Certificate III Captive Animal Management. Lecturers: Graeme Phipps, Jackie Salkeld, Brad Walker Chris Hosking Live Exhibit Keeper [email protected] www.australianmuseum.net.au/Live-Exhibits Australian Museum 6 College St, Sydney NSW 2010. Front cover image: Eastern Water Dragon, Physignathus lesueurii lesueurii. Photo: Rebekah Hosking. 2 DISCLAIMER These husbandry guidelines were produced by the compiler at TAFE NSW – Western Sydney Institute, Richmond College, N.S.W. Australia as part assessment for completion of Certificate III in Captive Animals, Course number 1068, RUV30204. Since the husbandry guidelines are the result of student project work, care should be taken in the interpretation of information therein, - in effect, all care taken but no responsibility is assumed for any loss or damage that may result from the use of these guidelines. It is offered to the ASZK Husbandry Manuals Register for the benefit of animal welfare and care. Husbandry guidelines are utility documents and are ‘works in progress’, so enhancements to these guidelines are invited. Image 1. Male Eastern Water Dragon. Photo: Rebekah Hosking 3 OCCUPATIONAL HEALTH AND SAFETY RISKS The Australian Water Dragon, Physignathus lesueurii, is generally not an aggressive lizard to maintain in captivity; however like all large Agamids they are capable of inflicting a severe bite when agitated. They can also use tail whips as a way to discourage unwanted attention when cornered. This species also possesses long sharp claws which can inflict serious lacerations which at minimum will require first aid or even medical treatment.