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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. -
APP203875 Submissions Compilation.Pdf
APP203875 German and Common wasps BCA Submissions 11 November 2020 Under section 34 of the Hazardous Substances and New Organisms Act 1996 Volume 1 of 1 to release 2 parasitoids, Metoecus paradoxus and Volucella inanis, as biological control agents for the invasive German and common wasps Submission Number Submitter Submitter Organisation SUBMISSION127659 Clinton Care SUBMISSION127660 Member of Public 01 SUBMISSION127661 Peter King SUBMISSION127662 Rod Hitchmough Department of Conservation SUBMISSION127663 Member of Public 02 SUBMISSION127664 Linde Rose SUBMISSION127665 Andrew Blick SUBMISSION127666 Shane Hona Bay of Plenty Regional Council SUBMISSION127667 Bryce Buckland SUBMISSION127668 Jono Underwood Marlborough District Council SUBMISSION127669 Kane McElrea Northland Regional Council - Whangarei SUBMISSION127670 Member of Public 03 SUBMISSION127671 Davor Bejakovich Greater Wellington Regional Council SUBMISSION127672 Margaret Hicks SUBMISSION127673 Jenny Dymock Northland Regional Council - Whangarei SUBMISSION127674 Member of Public 04 SUBMISSION127675 Roger Frost SUBMISSION127676 Ricki Leahy Trees and Bees Ltd SUBMISSION127677 Barry Wards Ministry for Primary Industries SUBMISSION127678 Member of Public 05 SUBMISSION127679 Jan O'Boyle 1 Submission Number Submitter Submitter Organisation Apiculture New Zealand Science and SUBMISSION127680 Sue Carter Research Focus Group SUBMISSION127681 Andrea Dorn SUBMISSION127682 Benita Wakefield Te Rūnanga o Ngāi Tahu SUBMISSION127683 Emma Edney-Browne Auckland Council SUBMISSION127684 David Hunter -
Protection of Pandora Moth (Coloradia Pandora Blake) Eggs from Consumption by Golden-Mantled Ground Squirrels (Spermophilus Lateralis Say)
AN ABSTRACT OF THE THESIS OF Elizabeth Ann Gerson for the degree of Master of Science in Forest Science presented on 10 January, 1995. Title: Protection of Pandora Moth (Coloradia pandora Blake) Eggs From Consumption by Golden-mantled Ground Squirrels (Spermophilus lateralis Say) Abstract approved: Redacted for Privacy William C. McComb Endemic populations of pandora moths (Coloradia pandora Blake), a defoliator of western pine forests, proliferated to epidemic levels in central Oregon in 1986 and increased dramatically through 1994. Golden-mantled ground squirrels (Spermophilus lateralis Say) consume adult pandora moths, but reject nutritionally valuable eggs from gravid females. Feeding trials with captive S. lateralis were conducted to identify the mode of egg protection. Chemical constituents of fertilized eggs were separated through a polarity gradient of solvent extractions. Consumption of the resulting hexane, dichloromethane, and water egg fractions, and the extracted egg tissue residue, was evaluated by randomized 2-choice feeding tests. Consumption of four physically distinct egg fractions (whole eggs, "whole" egg shells, ground egg shells, and egg contents) also was evaluated. These bioassays indicated that C. pandora eggs are not protected chemically, however, the egg shell does inhibit S. lateralis consumption. Egg protection is one mechanism that enables C. pandora to persist within the forest food web. Spermophilus lateralis, a common and often abundant rodent of central Oregon pine forests, is a natural enemy of C. pandora -
Evaluation of a Proposed Significant Natural Area at Mt Iron, Wanaka
EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA R3762 EVALUATION OF A PROPOSED SIGNIFICANT NATURAL AREA AT MT IRON, WANAKA Coprosma shrubland on the southwest faces at the Allenby Farms site, Mt Iron. Contract Report No. 3762 March 2017 (Revised and updated) Project Team: Kelvin Lloyd - Report author: vegetation and flora Mandy Tocher - Report author: herpetofauna Brian Patrick - Report author: invertebrates Prepared for: Allenby Farms Ltd P.O. Box 196 Wanaka 9343 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, 07-343-9018; email [email protected], www.wildlands.co.nz CONTENTS 1. INTRODUCTION 1 2. SITE CONTEXT 1 3. METHODS 1 4. ECOLOGICAL CONTEXT 4 5. INDIGENOUS VEGETATION AND HABITATS 5 5.1 Kānuka scrub and shrubland 5 5.2 Coprosma scrub and shrubland 6 5.3 Exotic grassland and herbfield 7 5.4 Swale turf 8 5.5 Cushionfield 8 6. FLORA 8 6.1 Species richness 8 6.2 Threatened and At Risk plant species 12 6.3 Pest plants 12 7. BIRDS 13 8. LIZARDS 14 8.1 Overview 14 8.2 “Remove from SNA” zone 14 8.3 Alternate SNA 18 9. INVERTEBRATES 18 9.1 Overview 18 9.2 Mixed Coprosma-dominant shrubland 18 9.3 Kānuka scrub and shrubland 19 9.4 Rock outcrop habitats 19 9.5 Open grassland and turf 19 10. PEST ANIMALS 20 11. ECOLOGICAL VALUES 20 11.1 District Plan (2009) - Section 6c Significance 20 11.2 Proposed District Plan - Section 6c Significance from Policy 33.2.1.9 22 11.3 Significance summary 23 12. -
Assessing the Invertebrate Fauna Trajectories in Remediation Sites of Winstone Aggregates Hunua Quarry in Auckland
ISSN: 1179-7738 ISBN: 978-0-86476-417-1 Lincoln University Wildlife Management Report No. 59 Assessing the invertebrate fauna trajectories in remediation sites of Winstone Aggregates Hunua quarry in Auckland by Kate Curtis1, Mike Bowie1, Keith Barber2, Stephane Boyer3 , John Marris4 & Brian Patrick5 1Department of Ecology, Lincoln University, PO Box 85084, Lincoln 7647 2Winstone Aggregates, Hunua Gorge Road, Red Hill 2110, Auckland 3Department of Nature Sciences, Unitec Institute of Technology, PO Box 92025, Auckland 1142. 4Bio-Protection Research Centre, Lincoln University, PO Box 85084, Lincoln 7647. 5Consultant Ecologist, Wildlands, PO Box 33499, Christchurch. Prepared for: Winstone Aggregates April 2016 Table of Contents Abstract……………………………………………………………………………………....................... 2 Introduction…………………………………………………………………………………………………… 2 Methodology…………………………………………………………………………………………………. 4 Results…………………………………………………………………………………………………………… 8 Discussion……………………………………………………………………………………………………. 31 Conclusion…………………………………………………………………………………………………… 37 Recommendations………………………………………………………………………………………. 38 Acknowlegdements……………………………………………………………………………………… 38 References…………………………………………………………………………………………………… 39 Appendix……………………………………………………………………………………………………… 43 1 Abstract This study monitored the invertebrates in restoration plantings in the Winstone Aggregates Hunua Quarry. This was to assess the re-establishment of invertebrates in the restoration planting sites and compare them with unplanted control and mature sites. This study follows on from -
Beginners' Guide to Macro Moths
NZ moths are special Moths can also be pests Why we need to trap the moths? Why do we need to study moths? More than 86% of the known moths Hīhue (the kūmara moth, Agrius Who benefits from Moths are mainly out at night, so Moths breed fast and have lots of in NZ are endemic. They only occur convolvuli) had a large impact on studying moths? most people don’t see how many offspring. There are lots of different in NZ so we have to look after kūmara crops and there are many there are or what’s happening moth species playing different roles them.. whakatauki written about the to them. Unfortunately we need in the ecosystem. Moths have links Beginners’ Guide to Society caterpillar and its capacity to eat. You & I specimens for identification. to lots of other species (e.g. plants, Macro Moths Why are moths important? birds, introduced pests, other Moths are a key part of the wider A more recent pest is the codling Nature Why we need standardised data? invertebrates). ecosystem and they sit in the moth (Cydia pomonella). Introduced If we all use the same type of trap Te Tuakoko centre of a complex food web. The from Europe, it attacks apples, (e.g. a Heath Moth Trap) we can If something is changing in the caterpillars are herbivores eating a pears, walnuts, and other fruit. compare data from different places ecosystem, moths are amongst the first creatures to respond. They range of native plants. Education and over time. With standardised Moths have a bad reputation for information we can all work are likely to be good indicators of Stories Where to get more information & help Many adult moths drink nectar eating clothes, especially natural together to keep an eye on the change. -
Lepidoptera: Geometridae: Larentiinae)
Blackwell Science, LtdOxford, UKAENAustralian Journal of Entomology1326-67562005 Australian Entomological Society 200544257278Original ArticleRevision of ScotocymaO Schmidt Australian Journal of Entomology (2005) 44, 257–278 Revision of Scotocyma Turner (Lepidoptera: Geometridae: Larentiinae) Olga Schmidt Zoologische Staatssammlung München, Münchhausenstraße 21, D-81247, München, Germany. Abstract The Australasian genus Scotocyma Turner is revised, containing the species S. albinotata (Walker), S. legalis (Warren), S. asiatica Holloway, S. scotopepla Prout, stat. n., S. manusensis Prout, stat. n., S. mimula (Warren), stat. n. and S. miscix Prout. Scotocyma euryochra Turner, syn. n., S. idioschema Turner, syn. n., S. ischnophrica Turner, syn. n. and S. transfixa Turner, syn. n. are regarded as synonyms of S. albinotata. Four species are described as new: S. samoensis, sp. n., S. sumatrensis, sp. n., S. rutilimixta, sp. n. and S. longiuncus, sp. n. Lectotypes are designated for S. scotopepla, S. manusensis and S. miscix. All species are illustrated, and keys to species and distribution maps are provided. A phylogenetic analysis was performed to test the monophyly of the genus and to examine distribution patterns of the species. A biogeographical discussion is included. The tribal position of the genus is clarified and relationships to closely related genera are discussed. Key words Australasian region, biogeography, distribution patterns, geometrid moths, Melanesian island arcs, phylogenetics, taxonomy, Xanthorhoini. INTRODUCTION Since Turner (1922), there have been few reviews of the Australasian genera of Larentiinae. Craw (1986, 1987) revised The genus Scotocyma Turner (1904) belongs to the large sub- the New Zealand species of the genera Notoreas Meyrick and family Larentiinae (Lepidoptera: Geometridae). The larentiine Helastia (Guenée). The Australian Anachloris Meyrick and moths have a worldwide distribution, with the highest species Australasian Chaetolopha Warren have been revised recently diversity in temperate regions. -
1 © Australian Museum. This Material May Not Be Reproduced, Distributed
AMS564/002 – Scott sister’s second notebook, 1840-1862 © Australian Museum. This material may not be reproduced, distributed, transmitted, cached or otherwise used without permission from the Australian Museum. Text was transcribed by volunteers at the Biodiversity Volunteer Portal, a collaboration between the Australian Museum and the Atlas of Living Australia This is a formatted version of the transcript file from the second Scott Sisters’ notebook Page numbers in this document do not correspond to the notebook page numbers. The notebook was started from both ends at different times, so the transcript pages have been shuffled into approximately date order. Text in square brackets may indicate the following: - Misspellings, with the correct spelling in square brackets preceded by an asterisk rendersveu*[rendezvous] - Tags for types of content [newspaper cutting] - Spelled out abbreviations or short form words F[ield[. Nat[uralists] 1 AMS564/002 – Scott sister’s second notebook, 1840-1862 [Front cover] nulie(?) [start of page 130] [Scott Sisters’ page 169] Note Book No 2 Continued from first notebook No. 253. Larva (Noctua /Bombyx Festiva , Don n 2) found on the Crinum - 16 April 1840. Length 2 1/2 Incs. Ground color ^ very light blue, with numerous dark longitudinal stripes. 3 bright yellow bands, one on each side and one down the middle back - Head lightish red - a black velvet band, transverse, on the segment behind the front legs - but broken by the yellows This larva had a very offensive smell, and its habits were disgusting - living in the stem or in the thick part of the leaves near it, in considerable numbers, & surrounded by their accumulated filth - so that any touch of the Larva would soil the fingers.- It chiefly eat the thicker & juicier parts of the Crinum - On the 17 April made a very slight nest, underground, & some amongst the filth & leaves, by forming a cavity with agglutinated earth - This larva is showy - Drawing of exact size & appearance. -
An Invertebrate Survey of Reserves, Covenants and Significant Remnants of Eastern Banks Peninsula in 2010-2011
An Invertebrate survey of reserves, covenants and significant remnants of eastern Banks Peninsula in 2010-2011 by Mike Bowie, Cathy Mountier, Barry Fox, Stephane Boyer, Roseanna Gamlen-Greene, Sam Brown, Jon Sullivan, Robert Hoare and Peter Johns Lincoln University Wildlife Management Report No. 25 ISSN: 1177-6242 (Print) ISSN: 1179-7738 (Digital) ISBN: 978-0-86476-269-6 (Print) ISBN: 978-0-86476-270-2 (Digital) Lincoln University Wildlife Management Report No. 25 An Invertebrate survey of reserves, covenants and significant remnants of eastern Banks Peninsula in 2010-2011 by Mike Bowie, Cathy Mountier, Barry Fox, Stephane Boyer, Roseanna Gamlen-Greene, Sam Brown, Jon Sullivan, Robert Hoare (Landcare Research) and Peter Johns (Canterbury Museum) Ecology Division P.O. Box 84 Lincoln University [email protected] Prepared for: Josef Langer Trust & Department of Conservation September 2011 An Invertebrate survey of reserves, covenants and significant remnants of eastern Banks Peninsula in 2010-2011 Abstract Reserves, covenants and bush remnants of the eastern side of Banks Peninsula were surveyed for invertebrates including ground beetles (carabids), weevils, spiders, moths, earthworms and snails. Sixteen carabid species were found including one new Holcaspis species. The six-eyed spider Periegops suterii was found in six sites. Light trapping moths identified 202 species with 122 from Hinewai Reserve alone. Soil sampling found 13 endemic species of worms. New species of millipedes (Diplopoda) and cranefly (Tipulidae) were also found. Recommendations for future research on Banks Peninsula are given. Introduction The Eastern side of Banks Peninsula was created by eruptions and subsequent erosion of the Akaroa volcano which was active between 9 and 8 million years ago (Wilson, 1992). -
Exhibition Catalogue Natural History Illustrations by Erin Forsyth, 2018
A Few Exhibition catalogue Natural history illustrations by Erin Forsyth, 2018 TABLE OF CONTENTS ABOUT THE WORKS 5 About the artist 7 How to use this catalogue 9 TERMS AND CONDITIONS OF SALE 10 Korimako, makomako, bellbird 13 Kākāriki, Red-crowned parakeet, (Cyanoramphus novaezelandiae) 15 Moko kākāriki, Auckland green gecko (Naultinus elegans) 17 Pekapeka-tou-roa, long-tailed bat (Chalinolobus tuberculatus) 19 Pekapeka-tou-roa, long-tailed bat (Chalinolobus tuberculatus) 21 Pekapeka-tou-roa, long-tailed bat (Chalinolobus tuberculatus) 23 Ngirungiru, miromiro, South Island tomtit (Petroica macrocephala macrocephala) male 25 Kakaruwai, South Island Robin (Petroica australis) 27 Tōrea pango, variable oystercatcher (Haematopus unicolor) 29 Kererū, NZ wood pigeon (Hemiphaga novaeseelandiae) 31 Kōtare, sacred kingfisher (Todiramphus sanctus) 33 Ruru, morepork (Ninox novaeseelandiae) 35 TŪī, parsons bird (Prosthemadera novaeseelandiae) 37 Kōkako, blue-wattled crow (Callaeas wilsoni) 41 Takahe, South Island Takahe (Porphyrio hochstetteri) 43 Tūturiwhatu, NZ Dotteral (Charadrius obscurus) 45 Whio, blue duck (Hymenolaimus malacorhynchos) 47 Kahukōwhai, yellow admiral (Vanessa itea) 49 Wētāpunga, Little Barrier (Hauturu-o-Toi) giant weta (Deinacrida heteracantha) 51 Kārearea, NZ falcon (Falco novaeseelandiae) 53 Common evening brown (Melanitis leda bankia) 55 Pepe pouri, Helms' butterfly or forest ringlet (Dodonidia helmsii) 59 Kahukōwhai, yellow admiral (Vanessa itea) & Kahukura, NZ red admiral (V. gonerilla gonerilla) 63 Pepe pouri, Butler's ringlet (Erebiola butleri) & pepe pouri, black mountain ringlet (Percnodaimon merula) 67 Pīwakawaka, fantail (Rhipidura fuliginosa) 73 Weka, woodhen (Gallirallus australis) 75 Carnivorous land snail (Powelliphanta superba) 77 MYRTACEAE Studies I & II (Diptych) 79 ABOUT THE WORKS These original works are from the exhibition ‘A Few’ - the third installment in an ongoing series of natural history illustrations depicting native and resident species of Aotearoa by Erin Forsyth. -
Neuroscience Needs Ethology: the Marked Example of the Moth Pheromone System
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 16 July 2020 doi:10.20944/preprints202007.0357.v1 Review Neuroscience needs ethology: the marked example of the moth pheromone system Hervé Thevenon 1 1 Affiliation: Spascia; [email protected] 2 Correspondence: [email protected] Abstract: The key premise of translational studies is that knowledge gained in one animal species can be transposed to other animals. So far translational bridges have mainly relied on genetic and physiological similarities, in experimental setups where behaviours and environment are often oversimplified. These simplifications were recently criticised for decreasing the intrinsic value of the published results. The inclusion of wild behaviour and rich environments in neuroscience experimental designs is difficult to achieve because no animal model has it all. As an example, the genetic toolkit of moths species is virtually non-existent when compared to C. elegans, rats, mice, or zebrafish, however the balance is reversed for wild behaviours. The ethological knowledge gathered about the moth was instrumental for designing natural-like auditory stimuli, that were used in association with electrophysiology in order to understand how moths use these variable sounds produced by their predators in order to trump death. Conversely, we are still stuck with understanding how male moths make sense of their complex and diffuse olfactory landscape in order to locate conspecific females up to several hundred meters away, and precisely identify a conspecific in a sympatric swarm in order to reproduce. This systemic review articulates the ethological knowledge pertaining to this unresolved problem and leverages the paradigm to gain insight into how male moths process sparse and uncertain environmental sensory information. -
Zoologische Mededelingen 78-02
A new species of the genus Aleiodes Wesmael from New Zealand (Hymenoptera: Braconidae: Rogadinae) C. van Achterberg, L. Berndt, E. Brockerhoff & J. Berry Achterberg, C. van, L. Berndt, E. Brockerhoff & J. Berry. A new species of the genus Aleiodes Wesmael from New Zealand (Hymenoptera: Braconidae: Rogadinae). Zool. Med. Leiden 78 (19), 31.xii.2004: 301-311, figs 1-40.— ISSN 0024-0672. C. van Achterberg, Afdeling Entomologie (Hymenoptera), Nationaal Natuurhistorisch Museum, Postbus 9517, 2300 RA Leiden, The Netherlands (e-mail: [email protected]). L. Berndt & E. Brockerhoff, Forest Research, P.O. Box 29237, Fendalton, Christchurch 8004, New Zealand (e-mail: [email protected] / [email protected]). J. Berry, New Zealand Arthropod Collection, Landcare Research, Private Bag 92170, Auckland, New Zealand (e-mail: [email protected]). Key words: Hymenoptera; Braconidae; Rogadinae; Aleiodes; New Zealand; Australasian; Oriental; East Palaearctic; new species; distribution; partial key; Geometridae; Ennominae; Declana floccosa; Pseudo- coremia suavis; Pseudocoremia fenerata. A new species of the genus Aleiodes Wesmael, 1838 (Braconidae: Rogadinae: Rogadini), A. declanae spec. nov. from New Zealand is described and illustrated. It has been reared from Declana floccosa Walker, Cleora scriptaria (Walker), Pseudocoremia suavis Butler and P. fenerata Felder & Rogenhofer (Geometridae: Ennominae). Introduction The second and third authors have been involved in compiling information on the parasitoids of an ennomine geometrid, Pseudocoremia suavis Butler, 1879, which had several large scale outbreaks in pine forests in New Zealand. One of the most common parasitoids proved to be an Aleiodes Wesmael, 1838 (Hymenoptera: Braconidae: Roga- dinae: Rogadini), which turned out to be a new species according to research by the first and last authors.