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A New Leaf-Mining Moth from New Zealand, Sabulopteryx Botanica Sp
A peer-reviewed open-access journal ZooKeys 865: 39–65A new (2019) leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. 39 doi: 10.3897/zookeys.865.34265 MONOGRAPH http://zookeys.pensoft.net Launched to accelerate biodiversity research A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae Robert J.B. Hoare1, Brian H. Patrick2, Thomas R. Buckley1,3 1 New Zealand Arthropod Collection (NZAC), Manaaki Whenua–Landcare Research, Private Bag 92170, Auc- kland, New Zealand 2 Wildlands Consultants Ltd, PO Box 9276, Tower Junction, Christchurch 8149, New Ze- aland 3 School of Biological Sciences, The University of Auckland, Private Bag 92019, Auckland, New Zealand Corresponding author: Robert J.B. Hoare ([email protected]) Academic editor: E. van Nieukerken | Received 4 March 2019 | Accepted 3 May 2019 | Published 22 Jul 2019 http://zoobank.org/C1E51F7F-B5DF-4808-9C80-73A10D5746CD Citation: Hoare RJB, Patrick BH, Buckley TR (2019) A new leaf-mining moth from New Zealand, Sabulopteryx botanica sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae), feeding on the rare endemic shrub Teucrium parvifolium (Lamiaceae), with a revised checklist of New Zealand Gracillariidae. ZooKeys 965: 39–65. https://doi.org/10.3897/ zookeys.865.34265 Abstract Sabulopteryx botanica Hoare & Patrick, sp. nov. (Lepidoptera, Gracillariidae, Gracillariinae) is described as a new species from New Zealand. It is regarded as endemic, and represents the first record of its genus from the southern hemisphere. Though diverging in some morphological features from previously de- scribed species, it is placed in genus Sabulopteryx Triberti, based on wing venation, abdominal characters, male and female genitalia and hostplant choice; this placement is supported by phylogenetic analysis based on the COI mitochondrial gene. -
Forest Health News No
forest health news No. 181, February 2008 ISSN 1175-9755 BUDDLEIA LEAF WEEVIL UPDATE indicate weevils become inactive and hide at high temperatures. However, large numbers of very small larvae and eggs were found As reported in an earlier FH News (FH News 169, January 2007) in mid-February at all sites. the buddleia leaf weevil, Cleopus japonicus, was released by Scion staff at five sites in North Island plantations from October 2006 to The weevil can be considered established at all sites as more than January 2007. Release sites were established in Whakarewarewa, two generations have been recorded, weevils were found after Kinleith, Lake Taupo, Esk, and Rawhiti Forests. These forests winter, and numbers have increased. Buddleia leaf weevil feeding were selected because they represent a range of different climatic has been found 145 m from the release plants at Kinleith and conditions. The sites have since been monitored closely for weevil 200 m from them at Lake Taupo. It is only early days, but feeding establishment, dispersal, and feeding damage to buddleia. Despite damage to some plants is impressive. Very heavy defoliation will many years of research in quarantine, how well the weevil would be needed, however, to reduce the vigorous growth of buddleia. do in New Zealand forests was uncertain. Further releases have been made in the Kaikoura area, Whanganui, In particular, we were interested to see if cleopus would survive Masterton, and Bay of Plenty between November 2007 and winter as adult weevils and/or pupae, and would larvae be found February 2008. in the cooler months. -
E.Quadrangulata
Durable Eucalypt Leaflet Series Eucalyptus quadrangulata Ian Nicholas and Paul Millen December 2012 Why grow durable eucalypts? New Zealand’s agricultural landscapes need sustainable land use options adapted to droughts and floods which complement pastoral farming while reducing soil erosion, improving water quality and habitat for native biodiversity. Eucalypts are renowned for their adaptability to droughty and eroding landscapes. They also provide excellent habitat for nectar-feeding birds and insects. With over 400 eucalypt species to select from there is a great opportunity to select appropriate species for the planting objective. With CCA (copper chrome arsenic)-treated wood now banned for many uses by the USA and several European countries, there are significant international and domestic markets for naturally-durable hardwoods. The wood properties of New Zealand grown durable eucalypts ensure they can replace CCA treated material for many uses and are also ideal for a wide range of agricultural and land-based industrial applications, particularly for posts, poles and utility cross-arms as well as heavy structural timbers. NZDFI (New Zealand Dryland Forests Initiative) has selected eucalypt species which can be sawn to produce durable hardwood. Using these species, NZDFI is committed to developing viable best-practice forest management systems to complement livestock farming. NZDFI wants to encourage planting durable hardwood forests and woodlots to protect steeplands and waterways, for shade and shelter, and to generate income from carbon credits and sustainable timber harvesting. Why NZDFI have selected E. quadrangulata? NZDFI have selected species that: • Produce highly durable timber (Class 1 and 2 Australian Standard, AS5606-2005) • Are drought tolerant • Coppice vigorously after fire and harvesting • Do not appear to spread as wildings • Have the potential to sequester carbon faster than pine on drylands • Provide nectar/pollen for native biodiversity. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Pheromone Trap Catch of Harmful Microlepidoptera Species in Connection with the Chemical Air Pollutants
International Journal of Research in Environmental Science (IJRES) Volume 2, Issue 1, 2016, PP 1-10 ISSN 2454-9444 (Online) http://dx.doi.org/10.20431/2454-9444.0201001 www.arcjournals.org Pheromone Trap Catch of Harmful Microlepidoptera Species in Connection with the Chemical Air Pollutants L. Nowinszky1, J. Puskás1, G. Barczikay2 1University of West Hungary Savaria University centre, Szombathely, Károlyi Gáspár Square 4 2County Borsod-Abaúj-Zemplén Agricultural Office of Plant Protection and Soil Conservation Directorate, Bodrogkisfalud, Vasút Street. 22 [email protected], [email protected] Abstract: In this study, seven species of Microlepidoptera pest pheromone trap collection presents the results of the everyday function of the chemical air pollutants (SO2, NO, NO2, NOx, CO, PM10, O3). Between 2004 and 2013 Csalomon type pheromone traps were operating in Bodrogkisfalud (48°10’N; 21°21E; Borsod-Abaúj- Zemplén County, Hungary, Europe). The data were processed of following species: Spotted Tentiform Leafminer (Phyllonorycter blancardella Fabricius, 1781), Hawthorn Red Midged Moth (Phyllonorycter corylifoliella Hübner, 1796), Peach Twig Borer (Anarsia lineatella Zeller, 1839), European Vine Moth (Lobesia botrana Denis et Schiffermüller, 1775), Plum Fruit Moth (Grapholita funebrana Treitschke, 1846), Oriental Fruit Moth (Grapholita molesta Busck, 1916) and Codling Moth (Cydia pomonella Linnaeus, 1758). The relation is linear, logarithmic and polynomial functions can be characterized. Keywords: Microlepidoptera, pests, pheromone traps, air pollution 1. INTRODUCTION Since the last century, air pollution has become a major environmental problem, mostly over large cities and industrial areas (Cassiani et al. 2013). It is natural that the air pollutant chemicals influence the life phenomena of insects, such as flight activity as well. -
Izatha (Insecta: Lepidoptera: Gelechioidea: Oecophoridae)
Hoare, R. J. B. 2010: Izatha (Insecta: Lepidoptera: Gelechioidea: Oecophoridae). Fauna of New Zealand 65, 201 pp. The Copyright notice printed on page 4 applies to the use of this PDF. This PDF is not to be posted on websites. Links should be made to: FNZ.LandcareResearch.co.nz EDITORIAL BOARD Dr R. M. Emberson, c/- Department of Ecology, P.O. Box 84, Lincoln University, New Zealand Dr M. J. Fletcher, Director of the Collections, NSW Agricultural Scientific Collections Unit, Forest Road, Orange, NSW 2800, Australia Dr R. J. B. Hoare, Landcare Research, Private Bag 92170, Auckland, New Zealand Dr M.-C. Larivière, Landcare Research, Private Bag 92170, Auckland, New Zealand Mr R. L. Palma, Natural Environment Department, Museum of New Zealand Te Papa Tongarewa, P.O. Box 467, Wellington, New Zealand SERIES EDITOR Dr T. K. Crosby, Landcare Research, Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 65 Izatha (Insecta: Lepidoptera: Gelechioidea: Oecophoridae) Robert J. B. Hoare Landcare Research, Private Bag 92170, Auckland 1142, New Zealand [email protected] with colour plates by B.E. Rhode Manaak i W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2010 4 Hoare (2010): Izatha (Insecta: Lepidoptera: Gelechioidea: Oecophoridae) Copyright © Landcare Research New Zealand Ltd 2010 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. -
Tree-Derived Stimuli Affecting Host-Selection Response of Larva and Adult Peach Twig Borers, Anarsia Lineatella (Zeller) (Lepidoptera: Gelechiidae)
TREE-DERIVED STIMULI AFFECTING HOST-SELECTION RESPONSE OF LARVA AND ADULT PEACH TWIG BORERS, Anarsia lineatella (ZELLER) (LEPIDOPTERA: GELECHIIDAE) Mark Christopher Sidney B.Sc, B.Ed, Simon Fraser University, 1999, 2004 THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQmEMENTS FOR THE DEGREE OF MASTER OF SCIENCE In the Department of Biological Sciences O Mark Christopher Sidney 2005 SEviOiu' FiiASEii I..u'iVEiiSIT'k' Summer 2005 All rights reserved. This work may not be reproduced in whole or in part, by photocopy or other means, without permission of the author. APPROVAL Name: Mark Christopher Sidney Degree: Master of Science Title of Thesis: Tree-derived stimuli affecting host-selection response of larva and adult peach twig borers, Anarsia lineatella (Zeller) (Lepidoptera: Gelechiidae) Examining Committee: Chair: Dr. E. Elle, Assistant Professor Dr. G. Gries, Professor Department of Biological Sciences, S.F.U. Dr. G. Judd, Research Scientist Agriculture and Agri-Food Canada, Summerland Dr. M. Winston, Professor Department of Biological Sciences, S.F.U. Dr. S. Lindgren, Professor Ecosystem Science and Management Program, University of Northern British Columbia Public Examiner Date Approved SIMON FRASER UNIVERSITY PARTIAL COPYRIGHT LICENCE The author, whose copyright is declared on the title page of this work, has granted to Simon Fraser University the right to lend this thesis, project or extended essay to users of the Simon Fraser University Library, and to make partial or single copies only for such users or in response to a request from the library of any other university, or other educational institution, on its own behalf or for one of its users. -
Foliage Insect Diversity in Dry Eucalypt Forests in Eastern Tasmania
Papers and Proceedings of the Royal Society of Tasmania, Volume 136, 2002 17 FOLIAGE INSECT DIVERSITY IN DRY EUCALYPT FORESTS IN EASTERN TASMANIA by H.J. Elliott, R. Bashford, S.J. Jarman and M.G. Neyland (with four tables, one text-figure and two appendices) ELLIOTT, H.]., BASHFORD, R., JARMAN,S.]' & NEYLAND, M.G., 2002 (3l:xii): Foliage insect diversity in dry eucalypt forests in eastern Tasmania. Papers and Proceedings ofthe Royal Society afTasmania 136: 17-34. ISSN 0080-4703. Forestry Tasmania, 79 Melville St., Hobart, Tasmania 7000, Australia. Species numbers and composition of the insect fauna occurring on trees and shrubs were studied in dry eucalypt forests in eastern Tasmania over nine years. In all, 1164 named and putative species representing 17 orders and 157 families were collected. The bulk of the species belonged to the orders Coleoptera (28%), Hymenoptera (25%), Hemiptera (18%), Lepidoptera (14%) and Diptera (10%). Of the species collected, 388 -- about one-third -- were identified at least to genus or species level. These included 21 named species not previously listed in the Tasmanian insect fauna and 90 undescribed species. A list of 22 host plants for 171 insect species was compiled from records of 132 insect species observed feeding during the study and from previous records ofinsect/host plant associations for 39 insect species found on the study plots. Most insects were feeding on eucalypts (127 insect species) and acacias (38 species). The most widely distributed and commonly collected species were several well-known pests ofeucalypts: Gonipterus scutellatus (Coleoptera: Curculionidae), Uraba lugens (Lepidoptera: N octuidae), Amorbus obscuricornis (Hemiptera: Coreidae), Chaetophyes compacta (Hemiptera: Machaerotidae) and Eriococcus coriaceous(Hemiptera: Eriococcidae). -
Biosecurity 29
Issue 29 • 1 August 2001 A publication of MAF Biosecurity Authority Expensive produce: $200 instant fines introduced p4 Also in this issue: Should pig feeding be regulated? BSE: an international public health, animal health and trade issue Precaution and the management of biosecurity risks More resources needed for international plant work security Import risk analysis for Cordyline and Dracaena Painted apple moth response report released Sudden oak death – new disease identified in US Developing codes of welfare: a consultative process Pipfruit industry certification post deregulation Biosecurity How to contact us: Contents Everyone listed at the end of an article as a contact point, unless otherwise indicated, is part of the Ministry of Agriculture and Forestry Biosecurity Authority. 3 Biosecurity takes a stand All MAF staff can be contacted by e-mail, FMD campaign wound up and the standard format for all addresses is 4 Cover story: Instant fines catch 454 travellers in first fortnight [email protected] For example Ralph Hopcroft would be New Zealand experts contribute to risk analysis text [email protected] (There are slight 5 Should pig feeding be regulated? exceptions for people with similar names, but these addresses are given where necessary.) 6 BSE: an international public health, animal health and trade issue 7 Varroa update: varroa control book published by MAF PO Box 2526, Wellington New Zealand 8 Biosecurity Council position statement on the application of precaution in managing biosecurity risks associated with -
Fhnews 168 Nov/Dec.P65
forest health news No. 168, November/December 2006 ISSN 1175-9755 UPDATE — ACROCERCOPS LACINIELLA — A EUCALYPTUS LEAF MINER Acrocercops laciniella (Gracillariidae), the blackbutt leaf miner, is an Australian species that was first found in New Zealand in 1999 near Auckland International Airport. It spread rapidly throughout the North Island and was detected in the South Island in 2004. It has subsequently been found in Marlborough (2005) and the Marlborough Sounds (2006). In Australia A. laciniella is widespread from southern Queensland to Tasmania and periodically causes severe damage to Eucalyptus pilularis in coastal New South Wales. Both mature and coppice foliage is damaged. In Tasmania it is common on the juvenile foliage of E. nitens, E. globulus, E. regnans, and E. obliqua. For further information and references, see Forest Health News 83. Prior to 1999 there were 12 species of Acrocercops known from New Zealand; 10 native species that mine the leaves of native hosts, and two other Australian species — A. alysidota (mines the Above: Acrocercops laciniella larva visible under the mine. Below: A. laciniella larva with top of the mine removed. phyllodes of Acacia) and A. eumetallica (lives in galls on Acacia). Perhaps two of the best known of the native species are A. leucocyma, the kauri leaf miner, and A. zorionella, the Coprosma leaf miner. Acrocercops laciniella has been recorded from more than 60 species of Eucalyptus in New Zealand and records in the Ensis Forest Health Database show that it is most common on Eucalyptus botryoides, E. fastigata, E. ficifolia, E. globulus, E. leucoxylon, E. nicholii, E. nitens, E. -
Gelechiidae Biosecurity Occurrence Background Subfamilies Short
Ardozyga stratifera (Gelechiinae) Gelechiidae Twirler Moths or Gelechiid Moths Biosecurity BIOSECURITY ALERT This Family is of Biosecurity Concern Occurrence This family occurs in Australia. Background The micromoth family Gelechiidae is the namesake family for the enormous superfamily Gelechioidea and is one of the most diverse families of the Lepidoptera. Gelechiids are very small moths with narrow wings. The family has a worldwide distribution and is diverse with over 4,700 known species in 500 genera, but that number would be at least doubled with undescribed and new species. The family is particularly prevalent in North America because of the close association of species with Douglas fir (Pseudotsuga). The caterpillars have very diverse feeding habits on many plant parts and species. Many species are external feeders but are protected by a shelter of some kind, often in tied or rolled leaves (Fig. 1). Many others feed internally, boring into flower heads, stems (Fig. 2) or roots. They are leaf-miners (Fig. 11), gall-inducers or stem-borers, or feed within flowers or fruits (Fig. 13). They also can be concealed in silken tunnels in earth or in portable cases. Not surprisingly, therefore, there are many gelechiids that are agricultural pests, such as: the pink bollworm, Pectinophora gossypiella (Fig. 13), one of the most destructive pests of cotton in the world; Sitotroga cerealella (Angoumois grain moth); Phthorimaea operculella (potato tuber moth); and, Tuta absoluta (tomato leaf miner). Contrastingly, several species have been used as biocontrol agents against weeds. One Australian species feeds on dead leaf litter. Fig. 1. Mature caterpillar of the widespread Australian gelechiid Ardozyga stratifera (Gelechiinae). -
In Victoria, the Incidence of Sirex Over Summer 2001-2002 Remained
Primary Industries Standing Committee Forestry and Forest Products Committee Research Priorities and Co-ordination Committee RESEARCH WORKING GROUP 7 FOREST HEALTH Annual Pest and Disease Status Report for Australia and New Zealand 2003-2004 October 2004 1 TABLE OF CONTENTS INTRODUCTION ..................................................................................................................................7 PURPOSE ...............................................................................................................................................7 AUSTRALIA ..........................................................................................................................................8 VICTORIA..............................................................................................................................................8 PLANTATIONS.......................................................................................................................................8 Pinus spp.........................................................................................................................................8 Insect Pests.................................................................................................................................................8 Sirex noctilio (Sirex wood wasp)..........................................................................................................8 Ips grandicollis (Fivespined Bark Beetle) and other bark beetle species ..............................................8