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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. -
Trees for Farm Forestry: 22 Promising Species
Forestry and Forest Products Natural Heritage Trust Helping Communities Helping Australia TREES FOR FARM FORESTRY: 22 PROMISING SPECIES Forestry and Forest Products TREES FOR FARM FORESTRY: Natural Heritage 22 PROMISING SPECIES Trust Helping Communities Helping Australia A report for the RIRDC/ Land & Water Australia/ FWPRDC Joint Venture Agroforestry Program Revised and Edited by Bronwyn Clarke, Ian McLeod and Tim Vercoe March 2009 i © 2008 Rural Industries Research and Development Corporation. All rights reserved. ISBN 1 74151 821 0 ISSN 1440-6845 Trees for Farm Forestry: 22 promising species Publication No. 09/015 Project No. CSF-56A The information contained in this publication is intended for general use to assist public knowledge and discussion and to help improve the development of sustainable regions. You must not rely on any information contained in this publication without taking specialist advice relevant to your particular circumstances. While reasonable care has been taken in preparing this publication to ensure that information is true and correct, the Commonwealth of Australia gives no assurance as to the accuracy of any information in this publication. The Commonwealth of Australia, the Rural Industries Research and Development Corporation (RIRDC), the authors or contributors expressly disclaim, to the maximum extent permitted by law, all responsibility and liability to any person, arising directly or indirectly from any act or omission, or for any consequences of any such act or omission, made in reliance on the contents of this publication, whether or not caused by any negligence on the part of the Commonwealth of Australia, RIRDC, the authors or contributors. The Commonwealth of Australia does not necessarily endorse the views in this publication. -
The Sweet Tooth of Adult Parasitoid <I>Cotesia Rubecula</I>: Ignoring
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications in the Biological Sciences Papers in the Biological Sciences 7-2004 The Sweet Tooth of Adult Parasitoid Cotesia rubecula: Ignoring Hosts for Nectar? Gitta Siekmann Federal Biological Research Centre for Agriculture and Forestry, Germany, [email protected] Michael A. Keller University of Adelaide, Australia, [email protected] Brigitte Tenhumberg University of Nebraska - Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/bioscifacpub Part of the Life Sciences Commons Siekmann, Gitta; Keller, Michael A.; and Tenhumberg, Brigitte, "The Sweet Tooth of Adult Parasitoid Cotesia rubecula: Ignoring Hosts for Nectar?" (2004). Faculty Publications in the Biological Sciences. 122. https://digitalcommons.unl.edu/bioscifacpub/122 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications in the Biological Sciences by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Published in Journal of Insect Behavior 17:4 (July 2004), pp. 459–476. Copyright © 2004 Springer Science+Business Media, Inc. Used by permission. Accepted April 19, 2003; revised March 30, 2004. The Sweet Tooth of Adult Parasitoid Cotesia rubecula: Ignoring Hosts for Nectar? Gitta Siekmann, Michael A. Keller, and Brigitte Tenhumberg Department of Applied and Molecular Ecology, The University of Adelaide, Waite Campus Private Bag 1, SA 5064 Glen Osmond, Australia Corresponding author — G. Siekmann. Present address: Institute for Plant Protection in Horticulture, Federal Biological Research Centre for Agriculture and Forestry, Messeweg 11-12, 38104 Braunschweig, Germany; email [email protected] Abstract Investing time and energy into survival and reproduction often presents a trade-off to many species of animals. -
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. -
Gumleaf Skeletoniser Biocontrol: a Lesson in Patience
THE JOINT FORCES OF CSIRO & SCION Lisa Berndt, Michelle Watson and Tara Murray Ensis Forest Biosecurity and Protection BiologicalBiological controlcontrol ofof gumleafgumleaf skeletoniser,skeletoniser, paropsisparopsis andand buddleiabuddleia March 2007 THE JOINT FORCES OF CSIRO & SCION Gumleaf skeletoniser Uraba lugens (Nolidae) • Australian eucalypt defoliator • In Auckland since 2001 • Spreading to Waikato, Northland, BOP • Threat to plantations, amenity trees, public health • Attacking new host plant species THE JOINT FORCES OF CSIRO & SCION GLS biocontrol • 4 potential parasitoids identified • ERMA permission to import 2004 • Develop rearing & host testing methods 2004-2007 (2 species) Eriborus sp. Photos: Geoff Allen & John Barran Euplectrus sp. Cotesia urabae Dolichogenidea eucalypti THE JOINT FORCES OF CSIRO & SCION Success: rearing • Rearing method finally successful • Solving mating problems key THE JOINT FORCES OF CSIRO & SCION Success: host testing • Methods developed • Nearly complete for two species • Nine more species to test • Strong preference for uraba THE JOINT FORCES OF CSIRO & SCION Paropsis biocontrol • Major eucalypt pest • Previously controlled by parasitoid Enoggera nissaui • Biocontrol disrupted by hyperparasitoid in North Island since 2002 Enoggera nassaui on P. charybdis egg • Second parasitoid (Neopolycystus insectifurax) not as effective • Most plantations sprayed annually now THE JOINT FORCES OF CSIRO & SCION Paropsis charybdis Current research • PhD student Tara Murray (2nd year) • Studying biology of hyperparasitoid -
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. -
The Influence of Induced Host Moisture Stress on the Growth and Development of Western Spruce Bud Worm and Armillaria Ostoyae on Grand Fir Seedlings
AN ABSTRACT OF THE THESIS OF Catherine Gray Parks for the degree of Doctor of Philosophy in the Department of Forest Science, presented on April 28, 1993. Title: The Influence of Induced Host Moisture Stress on the Growth and Development of Western Spruce Budworm and Armillaria ostoyae on Grand Fir Seedlings. Abstract Approved: John D. Waistad This greenhouse study evaluates the influence of separately and simultaneously imposed water stress, western spruce budworm (Choristorneura occidentalis Freeman) defoliation, and inoculation with the root pathogen, Armillaria ostoyae (Romagn.) Herink, on the growth and biochemical features of Abies .grandis (Dougl.) Lindi. Seedling biomass, plant moisture status, bud phenology, and allocation patterns of phenolics, carbohydrates, and key nutrients (nitrogen, phosphorus, potassium and sulfur) are reported. Hypotheses are developed and testedon the impacts of water-stress, defoliation, and root inoculation, on westernspruce budworm growth and development, and Armillaria ostoyae-caused mortality and infection. Western spruce budworm larvae fedon water-stressed seedlings had higher survival rates, grew faster, and produced largerpupae than those fed on well- watered seedlings. There is no clear reason for the positive insectresponse, but changes in foliage nutrient patterns and phenolic chemistryare indicated. Insect caused defoliation has been earlier reported to enhance successful colonization of Armillaria spp. on deciduous trees in the forests of the northeastern United States. The positive response of the fungus was attributed to a weakened tree condition. Conversely, although this study conclusively found water-limited trees to have increased susceptibility to A. ostoyae, defoliation significantly lowered Armillaria-caused infection and mortality. The decline in infection success is attributed to defoliation-caused reduction in plant water stress and an alteration of root carbohydrate chemistry. -
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). -
(Hymenoptera: Braconidae), a Parasitoid of Pieris Brassicae (L.) (Lepidoptera: Pieridae), As Affected by Experience
WAGENINGEN UNIVERSITY LABORATORY OF ENTOMOLOGY Host discrimination by Cotesia glomerata (L.) (Hymenoptera: Braconidae), a parasitoid of Pieris brassicae (L.) (Lepidoptera: Pieridae), as affected by experience No: 09.04 Name: Linda Heilmann Period: January 2004 – July 2004 Thesis: F050-707 1e Examinator: dr. ir. Joop A. van Loon 2e Examinator: dr. Nina E. Fatouros Contents 1. Introduction .................................................................................................................... 3 1.1. Host discrimination and superparasitism ................................................................ 3 1.2. Host searching by Cotesia glomerata ..................................................................... 5 1.2.1. Host microhabitat location ....................................................................... 5 1.2.2. Host location and host acceptance ............................................................ 7 1.3. Learning ............................................................................................................ 7 1.3.1. Learning in parasitoid wasps .................................................................... 7 1.3.2. Completeness of the information .............................................................10 1.3.3. Order of the information.........................................................................11 1.4. Previous research...............................................................................................11 2. Research questions .........................................................................................................12 -
Conservation Biology of Tile Marsh Fritillary Butterfly Euphydryas a Urinia
CONSERVATION BIOLOGY OF TILE MARSH FRITILLARY BUTTERFLY EUPHYDRYAS A URINIA CAROLINE ROSE BULMAN Submitted in accordance with the requirements for the degree of Doctor of Philosophy The University of Leeds School of Biology Centre for Biodiversity and Conservation September 2001 The candidate confirms that the work submitted is her own and that appropriate credit has been given where reference has been made to the work of others. 11 ACKNOWLEDGEMENTS I am indebted to Chris Thomas for his constant advice, support, inspiration and above all enthusiasm for this project. Robert Wilson has been especially helpful and I am very grateful for his assistance, in particular with the rPM. Alison Holt and Lucia Galvez Bravo made the many months of fieldwork both productive and enjoyable, for which I am very grateful. Thanks to Atte Moilanen for providing advice and software for the IFM, Otso Ovaskainen for calculating the metapopulation capacity and to Niklas Wahlberg and Ilkka Hanski for discussion. This work would have been impossible without the assistance of the following people andlor organisations: Butterfly Conservation (Martin Warren, Richard Fox, Paul Kirland, Nigel Bourn, Russel Hobson) and Branch volunteers (especially Bill Shreeve and BNM recorders), the Countryside Council for Wales (Adrian Fowles, David Wheeler, Justin Lyons, Andy Polkey, Les Colley, Karen Heppingstall), English Nature (David Sheppard, Dee Stephens, Frank Mawby, Judith Murray), Dartmoor National Park (Norman Baldock), Dorset \)Ji\thife Trust (Sharoii Pd'bot), )eNorI Cornwall Wildlife Trust, Somerset Wildlife Trust, the National Trust, Dorset Environmental Records Centre, Somerset Environmental Records Centre, Domino Joyce, Stephen Hartley, David Blakeley, Martin Lappage, David Hardy, David & Liz Woolley, David & Ruth Pritchard, and the many landowners who granted access permission. -
Hymenoptera: Braconidae: Microgastrinae) Comb
Revista Brasileira de Entomologia 63 (2019) 238–244 REVISTA BRASILEIRA DE Entomologia A Journal on Insect Diversity and Evolution www.rbentomologia.com Systematics, Morphology and Biogeography First record of Cotesia scotti (Valerio and Whitfield, 2009) (Hymenoptera: Braconidae: Microgastrinae) comb. nov. parasitising Spodoptera cosmioides (Walk, 1858) and Spodoptera eridania (Stoll, 1782) (Lepidoptera: Noctuidae) in Brazil a b a a Josiane Garcia de Freitas , Tamara Akemi Takahashi , Lara L. Figueiredo , Paulo M. Fernandes , c d e Luiza Figueiredo Camargo , Isabela Midori Watanabe , Luís Amilton Foerster , f g,∗ José Fernandez-Triana , Eduardo Mitio Shimbori a Universidade Federal de Goiás, Escola de Agronomia, Setor de Entomologia, Programa de Pós-Graduac¸ ão em Agronomia, Goiânia, GO, Brazil b Universidade Federal do Paraná, Setor de Ciências Agrárias, Programa de Pós-Graduac¸ ão em Agronomia – Produc¸ ão Vegetal, Curitiba, PR, Brazil c Universidade Federal de São Carlos, Programa de Pós-Graduac¸ ão em Ecologia e Recursos Naturais, São Carlos, SP, Brazil d Universidade Federal de São Carlos, Departamento de Ecologia e Biologia Evolutiva, São Carlos, SP, Brazil e Universidade Federal do Paraná, Departamento de Zoologia, Curitiba, PR, Brazil f Canadian National Collection of Insects, Ottawa, Canada g Universidade de São Paulo, Escola Superior de Agricultura “Luiz de Queiroz”, Departamento de Entomologia e Acarologia, Piracicaba, SP, Brazil a b s t r a c t a r t i c l e i n f o Article history: This is the first report of Cotesia scotti (Valerio and Whitfield) comb. nov. in Brazil, attacking larvae of the Received 3 December 2018 black armyworm, Spodoptera cosmioides, and the southern armyworm, S. -
Venom Gland Extract Is Not Required for Successful Parasitism in the Polydnavirus-Associated Endoparasitoid Hyposoter Didymator (Hym
Insect Biochemistry and Molecular Biology 43 (2013) 292e307 Contents lists available at SciVerse ScienceDirect Insect Biochemistry and Molecular Biology journal homepage: www.elsevier.com/locate/ibmb Venom gland extract is not required for successful parasitism in the polydnavirus-associated endoparasitoid Hyposoter didymator (Hym. Ichneumonidae) despite the presence of numerous novel and conserved venom proteins Tristan Dorémus a, Serge Urbach b, Véronique Jouan a, François Cousserans a, Marc Ravallec a, Edith Demettre b, Eric Wajnberg d, Julie Poulain c, Carole Azéma-Dossat c, Isabelle Darboux a, Jean-Michel Escoubas a, Dominique Colinet d, Jean-Luc Gatti d, Marylène Poirié d, Anne-Nathalie Volkoff a,* a INRA (UMR 1333), Université de Montpellier 2, “Insect-Microorganisms Diversity, Genomes and Interactions”, Place Eugène Bataillon, CC101, 34095 Montpellier Cedex, France b “Functional Proteomics Platform” BioCampus Montpellier, CNRS UMS3426, INSERM US009, Institut de Génomique Fonctionnelle, CNRS UMR5203, INSERM U661, Université de Montpellier 1 et 2, 34094 Montpellier, France c Commissariat à l’Energie Atomique (CEA), Institut de Génomique (IG), “Génoscope”, 2, rue Gaston-Crémieux, CP 5706, 91057 Evry, France d INRA (UMR 1355), CNRS (UMR 7254), Université Nice Sophia Antipolis, “Institut Sophia Agrobiotech” (ISA), 400 route des Chappes, 06903 Sophia Antipolis, France article info abstract Article history: The venom gland is a conserved organ in Hymenoptera that shows adaptations associated with life-style Received 25 October 2012 diversification. Few studies have investigated venom components and function in the highly diverse Received in revised form parasitic wasps and all suggest that the venom regulates host physiology. We explored the venom of the 21 December 2012 endoparasitoid Hyposoter didymator (Campopleginae), a species with an associated polydnavirus pro- Accepted 21 December 2012 duced in the ovarian tissue.