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Entomology of the Aucklands and Other Islands South of New Zealand: Lepidoptera, Ex Cluding Non-Crambine Pyralidae
Pacific Insects Monograph 27: 55-172 10 November 1971 ENTOMOLOGY OF THE AUCKLANDS AND OTHER ISLANDS SOUTH OF NEW ZEALAND: LEPIDOPTERA, EX CLUDING NON-CRAMBINE PYRALIDAE By J. S. Dugdale1 CONTENTS Introduction 55 Acknowledgements 58 Faunal Composition and Relationships 58 Faunal List 59 Key to Families 68 1. Arctiidae 71 2. Carposinidae 73 Coleophoridae 76 Cosmopterygidae 77 3. Crambinae (pt Pyralidae) 77 4. Elachistidae 79 5. Geometridae 89 Hyponomeutidae 115 6. Nepticulidae 115 7. Noctuidae 117 8. Oecophoridae 131 9. Psychidae 137 10. Pterophoridae 145 11. Tineidae... 148 12. Tortricidae 156 References 169 Note 172 Abstract: This paper deals with all Lepidoptera, excluding the non-crambine Pyralidae, of Auckland, Campbell, Antipodes and Snares Is. The native resident fauna of these islands consists of 42 species of which 21 (50%) are endemic, in 27 genera, of which 3 (11%) are endemic, in 12 families. The endemic fauna is characterised by brachyptery (66%), body size under 10 mm (72%) and concealed, or strictly ground- dwelling larval life. All species can be related to mainland forms; there is a distinctive pre-Pleistocene element as well as some instances of possible Pleistocene introductions, as suggested by the presence of pairs of species, one member of which is endemic but fully winged. A graph and tables are given showing the composition of the fauna, its distribution, habits, and presumed derivations. Host plants or host niches are discussed. An additional 7 species are considered to be non-resident waifs. The taxonomic part includes keys to families (applicable only to the subantarctic fauna), and to genera and species. -
Shifting Ranges of Two Tree Weta Species (Hemideina Spp.)
Journal of Biogeography (J. Biogeogr.) (2014) 41, 524–535 ORIGINAL Shifting ranges of two tree weta species ARTICLE (Hemideina spp.): competitive exclusion and changing climate Mariana Bulgarella*, Steven A. Trewick, Niki A. Minards, Melissa J. Jacobson and Mary Morgan-Richards Ecology Group, IAE, Massey University, ABSTRACT Palmerston North, 4442, New Zealand Aim Species’ responses to climate change are likely to depend on their ability to overcome abiotic constraints as well as on the suite of species with which they interact. Responses to past climate change leave genetic signatures of range expansions and shifts, allowing inferences to be made about species’ distribu- tions in the past, which can improve our ability to predict the future. We tested a hypothesis of ongoing range shifting associated with climate change and involving interactions of two species inferred to exclude each other via competition. Location New Zealand. Methods The distributions of two tree weta species (Hemideina crassidens and H. thoracica) were mapped using locality records. We inferred the likely mod- ern distribution of each species in the absence of congeneric competitors with the software Maxent. Range interaction between the two species on an eleva- tional gradient was quantified by transect sampling. Patterns of genetic diver- sity were investigated using mitochondrial DNA, and hypotheses of range shifts were tested with population genetic metrics. Results The realized ranges of H. thoracica and H. crassidens were narrower than their potential ranges, probably due to competitive interactions. Upper and lower elevational limits on Mount Taranaki over 15 years revealed expan- sion up the mountain for H. thoracica and a matching contraction of the low elevation limits of the range of H. -
Flawke's Bay Twits $ At\; Is T *:';;Q*E Kit *: Hawkt:Bad \, Nth U Line Uniat! of Species, Habitats Grid Natural Lectures
, , ,,,..*. *'.~,*, . , ** **~ I*~ tv, *..',.- 4'1 I, ' it**.*, , , *. * 44 ,,! ~**~ $1. \ -* * .,,;. f, *- , **, 3* .* ,J re* *. ^ ,~ I * ,* ,, ^ "*'. 441 , ,*.A, * ~*\,*t* J The open braids of the Totaekuri River Flawke's Bay twits $ at\; is t *:';;q*e Kit *: hawkt:bad \, nth u line uniat! of species, habitats Grid natural lectures. Hawke's Bay is a special part of New Zealand with a It, :ae from one threat can be exacerbated by the effects of variety of species, habitats and natural features, other threats acting together, i. e. habitat fragmentation Before humans settled here, almost the entire lowlands combined with invasive species. and hill country of the region would have been covered Despite extensive modification, Hawke's Bay contains a in dense forests, rich in birdlife. Clearance of vegetation great diversity of landscapes, habitats, plants, animals, cover started with early Maori and continued with and areas of high natural and historic value. There the arrival of Fakeba leaving a legacy of almost total are areas in Flawke's Bay which support a diverse and modification of the natural ecosystems. significant range of indigenous species and ecosystems including the Kaweka Ranges, Lake Walkaremoana, Forest dearance, wedand drainage, engineering of Pekapel<a Wetland, Whal{a}d Lagoon, AhuririEstuary, waterways and redamation of coastal margins has Blowhard Bush, Cape Kidnappers Sanctuary and been necessary for the development of our cities and Boundary Stream. Many of these sites are in very good the region. We are able to live safely and prosper in a condition. Several endemic species which at. e nationally beautiful part of the world but development has had a considerable impact on indigenous biodiversity. -
Weta Sometimes 5 Cicada Mouthparts? Earwig 3 Pairs Stick Insect 1 Pair with Fangs and Now Name One Poison Characteristic Each Wings? of the Other 6 Bugs Usually
Insects To be used with the Tangihua lions lodge program What is an insect All insects ? This insect have these has these Characteristics characteristics 6 legs What do you think? 8 legs More! Just circle the answer Wings Body parts? Or 2 No wings 3 A long thin body Legs? or 6 well developed legs 8 and long feelers More! I am a Eyes? Beetle 6 simple ones Fly 8 simple ones Moth Usually 2 but Giant Weta sometimes 5 Cicada Mouthparts? Earwig 3 pairs Stick insect 1 pair with fangs and Now name one poison characteristic each Wings? of the other 6 bugs Usually Draw a line showing who relates to what What habitats do you find insects in Weta To be used with the Tangihua lions lodge program Animals With out red blood or back bone Red blooded Invertebrates vertebrates Cephalopods Crustaceans Arthropod Plant animals Birds Fish Whales and Reptiles Land Cnidarians dolphins mammals Insects spider Wētā are arthropods and belong to the insect group because they have: 6 legs, 2 antennae, and a 3-part body Weta 5 types Tree Weta Ground Weta Giant Weta Tusked Weta Cave Weta Weta ? two compound eyes for close-up sight have these and three little eyes called ocelli to sense light and dark Antenna short tail-pieces called cerci to detect Femur vibrations Hind leg females have a long ovipositor at the- back to deposit eggs into the soil Front leg an ear on each front leg knee joint Ear palps alongside the jaws for tasting Ovipositor and smelling (like our tongue and nose) Spiracles spikey back legs that kick into the air Palps for defence and make a rasping sound as they come back down. -
Lepidoptera: Tortricidae: Tortricinae) and Evolutionary Correlates of Novel Secondary Sexual Structures
Zootaxa 3729 (1): 001–062 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Monograph ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3729.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:CA0C1355-FF3E-4C67-8F48-544B2166AF2A ZOOTAXA 3729 Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures JASON J. DOMBROSKIE1,2,3 & FELIX A. H. SPERLING2 1Cornell University, Comstock Hall, Department of Entomology, Ithaca, NY, USA, 14853-2601. E-mail: [email protected] 2Department of Biological Sciences, University of Alberta, Edmonton, Canada, T6G 2E9 3Corresponding author Magnolia Press Auckland, New Zealand Accepted by J. Brown: 2 Sept. 2013; published: 25 Oct. 2013 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 JASON J. DOMBROSKIE & FELIX A. H. SPERLING Phylogeny of the tribe Archipini (Lepidoptera: Tortricidae: Tortricinae) and evolutionary correlates of novel secondary sexual structures (Zootaxa 3729) 62 pp.; 30 cm. 25 Oct. 2013 ISBN 978-1-77557-288-6 (paperback) ISBN 978-1-77557-289-3 (Online edition) FIRST PUBLISHED IN 2013 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2013 Magnolia Press 2 · Zootaxa 3729 (1) © 2013 Magnolia Press DOMBROSKIE & SPERLING Table of contents Abstract . 3 Material and methods . 6 Results . 18 Discussion . 23 Conclusions . 33 Acknowledgements . 33 Literature cited . 34 APPENDIX 1. 38 APPENDIX 2. 44 Additional References for Appendices 1 & 2 . 49 APPENDIX 3. 51 APPENDIX 4. 52 APPENDIX 5. -
Male Tree Weta Are Attracted to Cuticular Scent Cues but Do Not Discriminate According to Sex Or Among Two Closely Related Species
Received: 26 April 2017 | Revised: 7 June 2017 | Accepted: 3 July 2017 DOI: 10.1111/eth.12652 RESEARCH PAPER Male tree weta are attracted to cuticular scent cues but do not discriminate according to sex or among two closely related species Priscilla M. Wehi1,2 | Adrian Monks2 | Mary Morgan-Richards1 1Institute of Agriculture & Environment, Massey University, Palmerston North, Abstract New Zealand Recognition of conspecifics is an essential precursor of successful mating. Where 2 Landcare Research, Dunedin, New Zealand related species coexist, species discrimination might be important, but because related Correspondence species are similar, species signal recognition may actually be low. Chemical cues such Priscilla M. Wehi, Landcare Research, Private as cuticular hydrocarbons (CHCs) are frequently used by insects to identify suitable Bag 1930 Dunedin, 9054 New Zealand. Email: [email protected] sexual partners. We predicted that New Zealand tree weta (Hemideina spp.), a genus Funding information of nocturnal ensiferan Orthoptera that live both allopatrically and sympatrically, use This work was supported by New Zealand chemical signals from either frass or CHCs to find mates. In a series of six laboratory Foundation for Research, Science and Technology contract number UOWX0501, trials using both H. thoracica and H. crassidens, we found that male tree weta, but not and Postdoctoral fellowship MAUX0905; female tree weta, occupied cavities primed with female cuticular cues more often than Rutherford Discovery Fellowship 14- LCR- 001 to PMW; and Massey University MURF cavities without. However, males did not discriminate between chemical cues of male funding “What limits a weta?” to MMR. and female conspecifics, or between conspecifics and heterospecifics. -
REPORT on APPLES – Fruit Pathway and Alert List
EU project number 613678 Strategies to develop effective, innovative and practical approaches to protect major European fruit crops from pests and pathogens Work package 1. Pathways of introduction of fruit pests and pathogens Deliverable 1.3. PART 5 - REPORT on APPLES – Fruit pathway and Alert List Partners involved: EPPO (Grousset F, Petter F, Suffert M) and JKI (Steffen K, Wilstermann A, Schrader G). This document should be cited as ‘Wistermann A, Steffen K, Grousset F, Petter F, Schrader G, Suffert M (2016) DROPSA Deliverable 1.3 Report for Apples – Fruit pathway and Alert List’. An Excel file containing supporting information is available at https://upload.eppo.int/download/107o25ccc1b2c DROPSA is funded by the European Union’s Seventh Framework Programme for research, technological development and demonstration (grant agreement no. 613678). www.dropsaproject.eu [email protected] DROPSA DELIVERABLE REPORT on Apples – Fruit pathway and Alert List 1. Introduction ................................................................................................................................................... 3 1.1 Background on apple .................................................................................................................................... 3 1.2 Data on production and trade of apple fruit ................................................................................................... 3 1.3 Pathway ‘apple fruit’ ..................................................................................................................................... -
Using Artificial Refuges to Translocate and Establish Auckland Tree Weta Hemideina Thoracica on Korapuki Island, New Zealand
Conservation Evidence (2005) 2, 94-95 www.ConservationEvidence.com Using artificial refuges to translocate and establish Auckland tree weta Hemideina thoracica on Korapuki Island, New Zealand Green C. Department of Conservation, PO Box 10420, The Terrace, Wellington 6143, New Zealand SUMMARY Two hundred wooden refuges were provided for the Auckland tree weta Hemideina thoracica . Within six months over half were used, 52 weta were transferred to Korapuki Island by plugging then translocating these refuges. After five years, there were over 500 individual tree wetas present on Korapuki. BACKGROUND habitat modification led to the loss of a variety of birds, lizards and large bodied invertebrates The Auckland tree weta Hemideina thoracica from Korapuki, including the Auckland tree (Orthoptera: Anostostomatidae) is a common weta. Restoration activities began with the species widely distributed over the upper half eradication of rats in 1987. Subsequently a of the North Island and its offshore islands, variety of native skink species were New Zealand. Their eggs hatch in spring and reintroduced through translocation from weta take 13 – 15 months to mature going neighbouring islands that had escaped invasion through eight to ten instars, with adults by the Pacific rat. In addition the island has reaching about 50 - 60 mm body length. been used to test new methods of invertebrate Although omnivorous, tree weta generally feed monitoring and translocation techniques, on fresh foliage in the canopy of forest trees particularly using artificial weta refuges and shrubs, with occasional fruit, flowers and designed to facilitate both these techniques. other invertebrates augmenting their diet. Thus the project aimed to re-establish the Typically tree weta hide during the day by Auckland tree weta on Korapuki Island using squeezing themselves into refuges such as a artificial refuges. -
Of New Zealand (Hemideina: Stenopelmatidae: Orthoptera)
New Zealand Entomologist, 1995, Val. 18 A new species of tree weta from the North Island of New Zealand (Hemideina: Stenopelmatidae: Orthoptera) MARYMORGAN-RICHARDS School of Biological Sciences, Victoria University of Wellington, PO Box 600, Wellington, New Zealand. ABSTRACT Hemideina trewicki, a new species of Stenopelmatidae from Hawkes Bay, is described. Morphologically it differs from H. crassidens only in the colouration of the pronotum but it can be distinguished using two allozyme loci (Ldh-2 and Pgm-I) and the number and gross morphology of the chromosomes. H. trewicki can be sympatric with H. thoracica and although a (probably sterile) F1 hybrid has been found, these two species have four fixed allozyme differences and karyotypes which clearly distinguish them. Keywords: tree weta, cryptic species, Hemideina crassidens, Hemideina thoracica, Hemideina treruicki, Orthoptera, Stenopelmatidae, New Zealand, karyotype, allozyme. INTRODUCTION Two species of tree weta are common and widespread in the North Island: Hemideina thoracica White, 1845 (Auckland tree weta) in the north to about 41 OS and H. crassidens (Rlanchard 1851) (Wellington tree weta) south of Mt Taranaki and Mt Ruapehu (Trewick & Morgan-Richards in press). Much confusion existed over their nomenclature until Ramsay & Bigelow (1978) clarified the situation. Since its original description, H. crassidens has been twice included in revisions where descriptions can be found under different names; Hutton (1897) referred to it as H. megacephala and Salmon (1950) as H. thoracica. Karny (1934), perhaps the last worker to examine the holotype, distinguished H. crassidem from H. thoracica by the presence of abdominal bands and a dark pronotum. In contrast the pronotum of H. -
Diagnoses and Remarks on the Genera of Tortricidae (Lepidoptera)
Acta zoologica cracoviensia, 58(2): 195-252, Kraków, 31 December, 2015 Ó Institute of Systematics and Evolution of Animals, Pol. Acad. Sci., Kraków doi:10.3409/azc.58_2.195 DiagnosesandremarksonthegeneraofTortricidae (Lepidoptera). Part3.Archipini JózefRAZOWSKI Received:15July2015.Accepted:21December2015.Availableonline:31December2015. RAZOWSKI J. 2015. Diagnoses and remarks on the genera of Tortricidae (Lepidoptera). Part3.Archipini. Actazool.cracov., 58(2): 195-252. Abstract. Comparative diagnoses, redescriptions, and remarks are presented on the genera of the tribe Archipini. Original references, type species, synonyms, numbers of known species, and zoogeographic regions are provided. Merophyas COMMON, 1964, is synoni- mizedwith Clepsis GUENÉE,1845. Keywords:Lepidoptera,Tortricidae,Archipini,genera,comparativediagnoses. Józef RAZOWSKI, Insitute of the Systematics and Evolution of Animals, Polish Academy * ofSciences, S³awkowska17, 31-016Kraków,Poland. E-mail:[email protected] I.INTRODUCTION The number of genera of Tortricidae has increased dramatically over last 50 years; by 2007 there were over 1630 described genera, including synonyms. Many of the older de- scriptions are scattered throughout the literature, and because there are few larger synthetic treatments of the tortricids for most major biogeographic regions, this large number of taxa complicates considerably the work of taxonomists on the faunas of poorly known regions of the planet. In addition, characters that define many of the genera are not clearly articu- lated. The distribution of many genera is still insufficiently known, and this shortcoming frequently results in unexpected findings, e.g., the discovery of Afrotropical genera in the Neotropics. These types of discoveries may cause confusion for specialists that focus on thefaunaofasinglegeographicregion. The literature abounds with re-descriptions and diagnoses of tortricid genera, but many are rather short, frequently lacking comparisons with similar or related taxa. -
Orthoptera: Ensifera)?
Zootaxa 4291 (1): 001–033 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4291.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:BD31B828-E7EF-46AD-B618-1BAAA2D63DBD Tackling an intractable problem: Can greater taxon sampling help resolve relationships within the Stenopelmatoidea (Orthoptera: Ensifera)? AMY G. VANDERGAST1,7, DAVID B. WEISSMAN2, DUSTIN A. WOOD3, DAVID C. F. RENTZ4, CORINNA S. BAZELET5 & NORIHIRO UESHIMA6 1U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, 4165 Spruance Road Suite 200, San Diego, CA 92101, USA. E-mail: [email protected] 2Department of Entomology, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA. E-mail: [email protected] 3U.S. Geological Survey, Western Ecological Research Center, San Diego Field Station, 4165 Spruance Road Suite 200, San Diego, CA 92101, USA. E-mail: [email protected] 4School of Marine & Tropical Biology, James Cook University, Australia. E-mail: [email protected] 5Steinhardt Museum, Tel Aviv University, Department of Zoology, Sherman Building Rm. 403, Tel Aviv, Israel; Department of Conser- vation Ecology and Entomology, Stellenbosch University, Private Bag X1, Matieland 7602, South Africa. E-mail: [email protected] 61435-1 Kubocho, Matsusaka, Mie 515-0044, Japan. E-mail: [email protected] 7Corresponding Author Abstract The relationships among and within the families that comprise the orthopteran superfamily Stenopelmatoidea (suborder Ensifera) remain poorly understood. We developed a phylogenetic hypothesis based on Bayesian analysis of two nuclear ribosomal and one mitochondrial gene for 118 individuals (84 de novo and 34 from GenBank). -
Conservation Status of the New Zealand Lepidoptera
Conservation status of the New Zealand Lepidoptera SCIENCE FOR CONSERVATION 136 B.H. Patrick and J.S. Dugdale Published by Department of Conservation P.O. Box 10-420 Wellington, New Zealand Science for Conservation presents the results of investigations by DOC staff, and by contracted science providers outside the Department of Conservation. Publications in this series are internally and externally peer reviewed. © January 2000, Department of Conservation ISSN 11732946 ISBN 047821867-2 Patrick, B. H. (Brian H.) Conservation status of the New Zealand Lepidoptera / B.H. Patrick and J.S. Dugdale. Wellington, N.Z. : Dept. of Conservation, 2000. 1 v. ; 30 cm. (Science for conservation, 1173-2946 ; 136). Cataloguing-in-Publication data. - Includes bibliographical references. ISBN 0478218672 1. Lepidoptera--New Zealand. I. Dugdale, J. S. II. Title. Series: Science for conservation ; 136. CONTENTS Abstract 5 1. Introduction 6 2. Construction of the list 7 2.1 The modified criteria of Molloy & Davis (1994) 7 2.2 Definitions of the Patrick & Dugdale categories 8 2.3 List format 9 2.4 Unevaluated species 10 3. Results and discussion 11 3.1 Numbers of species at risk 11 3.2 Habitats of the listed Lepidoptera 13 3.3 Need for more information 13 4. Conclusions 15 4.1 Species in urgent need of conservation action 15 5. Recommendations 16 6. Acknowledgements 17 7. References 18 8. Appendix 1. List of Lepidoptera species considered to be at risk 19 Conservation status of the New Zealand Lepidoptera B.H. Patrick and J.S. Dugdale Otago Museum, PO Box 6202, Dunedin, and 4 Montrose Drive, Nelson ABSTRACT The New Zealand moths and butterflies (Lepidoptera), forming New Zealands third largest Order of Insecta, with c.