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The First New Zealand Insects Collected on Cook's
Pacific Science (1989), vol.43, 43, nono.. 1 © 1989 by UniversityUniversity of Hawaii Press.Pres s. All rights reserved TheThe First New Zealand Zealand InsectsInsects CollectedCollectedon Cook'sCook's Endeavour Voyage!Voyage! 2 J. R. H. AANDREWSNDREWS2 AND G.G . W. GIBBSGmBS ABSTRACT:ABSTRACT: The Banks collection of 40 insect species, species, described by J. J. C.C. Fabricius in 1775,1775, is critically examined to explore the possible methods of collection and to document changesto the inseinsectct fauna andto the original collection localities sincsincee 1769.The1769. The aassemblagessemblageof species is is regarded as unusual. unusual. It includes insects that are large large and colorful as well as those that are small and cryptic;cryptic; some species that were probably common were overlooked, but others that are today rare were taken.taken. It is concluded that the Cook naturalists caught about 15species with a butterfly net, but that the majority (all CoColeoptera)leoptera) were discoveredin conjunction with other biobiologicallogical specimens, especially plantsplants.. PossibPossiblele reasons for the omission ofwetwetasas,, stick insects, insects, etc.,etc., are discussed. discussed. This early collection shows that marked changesin abundance may have occurred in some speciespeciess since European colonizationcolonization.. One newrecord is is revealed:revealed: The cicada NotopsaltaNotopsaltasericea sericea (Walker) was found to be among the Fabricius specispeci mens from New Zealand,Zealand, but itsits description evidentlyevidently -
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). -
Forest and Timber Insects in New Zealand No
Forest and Timber Insects in New Zealand No. 44 Large Cicadas Insect: Amphipsalta zelandica (Boisduval) (Hemiptera: Cicadidae) Amphipsalta cingulata (Fabricius) Amphipsalta strepitans (Kirkaldy) Based on M. K. Kay (1980) Fig. 1 - Adult Amphipsalta zelandica male. Type of injury Young cicadas (nymphs) and adults both have piercing-sucking mouth- parts with which they take up plant sap. Nymphs live in the soil and feed on roots while adults feed on above-ground parts of plants, but this seems to have little effect on plant growth. The major damage is caused by the female piercing plant tissues with her ovipositor to lay eggs. The cuts made by the three species of Amphipsalta form a herring-bone pattern (Fig. 2), and twigs and branches so affected may be sufficiently weakened to break in high winds. Such broken branches on conifers show up as reddish "flags" in the canopy when the foliage dies. Open cuts also provide entry for pathogens and wood- boring insects. Often the cuts heal over (Fig. 3) making the twigs gnarled in appearance. Ent_44_Amphipsalta_spp.doc Page 1 Fig. 2 - "Herring-bone" scars made by a female Amphipsalta when egglaying. The branch is of Eucalyptus ovata. Fig. 3 - Old egglaying damage. This Clerodendron twig has been cut to reveal calloused scar and ton egg deposition sites. Ent_44_Amphipsalta_spp.doc Page 2 Fig. 4 - Amphipsalta zelandica male above, female below. Hosts Amphipsalta females damage a wide range of native and exotic hardwood and softwood trees and shrubs. Distribution All cicadas in New Zealand are natives. Amphipsalta zelandica occurs throughout the country apart from central Otago and parts of Canterbury. -
An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant. -
Integrative Approach Unravels the Evolutionary History of Western Mediterranean Small Cicadas (Hemiptera: Cicadettini)
UNIVERSIDADE DE LISBOA FACULDADE DE CIÊNCIAS DEPARTAMENTO DE BIOLOGIA ANIMAL Integrative approach unravels the evolutionary history of Western Mediterranean small cicadas (Hemiptera: Cicadettini) Gonçalo João Barreto da Costa Mestrado em Biologia Evolutiva e Desenvolvimento Dissertação orientada por: Prof. Doutor Octávio Paulo Profª. Doutora Paula Simões 2017 "In the end we will conserve only what we love, we will love only what we understand, and we will understand only what we are taught." Baba Dioum Agradecimentos Antes de mais quero agradecer aos meus orientadores, Octávio Paulo e Paula Simões, por me terem apoiado durante este extenso (!) período de orientação. À Prof. Paula por me ter confiado as suas belas cigarras de Marrocos, e ter-me dado a oportunidade única de olhar com olhos de ver a sua colecção bem completa de cigarras mesmo interessantes! E falando em olhos... Por me ter emprestado os seus na descrição das cores das cigarras... Sem a Professora as cigarras ficavam-se por castanhas e pronto! A sua dedicação, boa disposição e acessibilidade quase ubíqua às minhas perguntas permitiu-me avançar sempre com o trabalho e com a escrita. O Prof. Octávio, chefe do grupo, já é conhecido pela genialidade quem tem em analisar os dados e ver para lá do que nos parece óbvio! Comprovei que é bem verdade quando trouxe dados preliminares do BEAST e o Professor para além de ver aquilo que era óbvio conseguiu ver para além lá daquela primeira camada e adicionar muito mais informação que aquela que conseguiria observar. Ainda que o Professor estivesse sempre 125% do tempo ocupado sempre conseguia arranjar um tempo para discutir novos métodos, novas abordagens aos meus datasets, novos artigos e resultados. -
Auchenorrhyncha (Insecta: Hemiptera): Catalogue
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 63 Auchenorrhyncha (Insecta: Hemiptera): catalogue M.-C. Larivière1, M. J. Fletcher2, and A. Larochelle3 1, 3 Landcare Research, Private Bag 92170, Auckland, New Zealand 2 Industry & Investment NSW, Orange Agricultural Institute, Orange NSW 2800, Australia 1 [email protected], 2 [email protected], 3 [email protected] with colour photographs by B. E. Rhode Manaaki W h e n u a P R E S S Lincoln, Canterbury, New Zealand 2010 4 Larivière, Fletcher & Larochelle (2010): Auchenorrhyncha (Insecta: Hemiptera) 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. -
Sexual Signaling in Periodical Cicadas, Magicicada Spp. (Hemiptera: Cicadidae)
SEXUAL SIGNALING IN PERIODICAL CICADAS, MAGICICADA SPP. (HEMIPTERA: CICADIDAE) by JOHN R. COOLEY1,2) and DAVID C. MARSHALL1,3) (Department of Biology and Museum of Zoology, University of Michigan, Ann Arbor, MI 48109-1079) (Acc. 4-VI-2001) Summary Periodical cicada (Magicicada spp.) sexual pair formation takes place in dense aggregations and involves intense male-male competition for limited mating opportunities. Pair-forming behavior in these species has been poorly understood because of limited knowledge of sexual communication. We have found that sexually receptive female Magicicada ick their wings in timed response to an individual chorusing male; this previously unrecognized female response is hereafter referred to as a ‘wing- ick’ signal. We document the nature, timing, and species-speci city of this signal as well as its absence in both immature and mated females. We also document changes in male chorusing and searching behavior in response to wing- ick signals and male responses to the signals’ visual and acoustical components. We test the hypothesis that female sensory psychology has shaped the evolution of -decim calls by 1) Current address: Department of Ecology and Evolutionary Biology, University of Connecticut, 75 North Eagleville Road, Storrs CT 06269-3043. 2) Corresponding author; e-mail address: [email protected] 3) We thank R.D. Alexander, T.E. Moore, D. Otte, C. Simon, K. Wells, and two anonymous reviewers for helpful discussion and comments. Thanks also to the Alum Springs Young Life Camp, Rockbridge County, VA; Horsepen Lake State Wildlife Management Area, Buckingham County, VA; Siloam Springs State Park, Brown and Adams Counties, IL; Harold E. -
Chorus Cicada, Amphipsalta Zelandica (Boisduval), Males Calling with Only Wing-Clicks
The Weta 43: 15-20 15 Chorus Cicada, Amphipsalta zelandica (Boisduval), males calling with only wing-clicks Kathy B. R. Hill Ecology and Evolutionary Biology, University of Connecticut, 75 N. Eagleville Rd U-3043, Storrs, CT 06269, USA. Email: [email protected] Over the past decade researchers from Professor Chris Simon’s lab (University of Connecticut, USA) have conducted field work during the summers to study and collect New Zealand cicadas. On three occasions, at three different locations, a single male Amphipsalta zelandica (Boisduval) was noted making wing-clicks (sometimes called wing-claps or wing- bangs) without accompanying timbal noise. Anecdotes from the public occasionally state that sometimes all one can hear is a loud hiss of wing-clicks from these noisy cicadas, however we have assumed that in such cases the observers are only paying attention to the loud, clicky part of the sound. At all times when we have heard choruses of A. zelandica, both timbal noise and wing-click sounds have been present, and our total observations include more than 350 individually noted locations throughout New Zealand. On three occasions during our field work, however, the author heard a single male A. zelandica making wing-clicks but no timbal noise, for approximately one minute or longer [Wellington: Day’s Bay walking track to Wainuiomata, 02 Mar 2002; Westland: Lake Mahinapua recreation area, S of Hokitika, 16 Feb 2011; Westland: Gillespies Beach, W of Fox Glacier, 06 Feb 2012]. These observations were at approximate distances of ~10m, 3m and <1m respectively. Unfortunately none of these individuals was collected, but the one at Gillespies Beach was sighted and noted to be definitely a male. -
Xylella Review
1 Risks to New Zealand’s primary industries from Xylella Mette Nielsen, Kerry Everett, Virginia Marroni, Glen Greer, Simon Bulman Summary Background The bacterium Xylella fastidiosa is a plant pathogen of worldwide biosecurity concern. This review aims to describe the potential biosecurity threat of X. fastidiosa to New Zealand’s valued plant systems. The work seeks to build awareness of the threat posed by X. fastidiosa across industry, government, research providers and tangata whenua in order to prioritise readiness activities that would minimise its impact upon incursion. Key findings from the review are: Pathogen • X. fastidiosa is an obligate inhabitant of plant xylem vessels that also colonises the foregut of xylem-sap feeding insect vectors. • Genomic research shows that X. fastidiosa can be divided into genetically distinct subspecies: ssp. fastidiosa, ssp. multiplex, ssp. pauca, ssp. morus, ssp. sandyi which have evolved in different regions of the Americas. • Plant diseases are associated with specific subspecies and host combinations. Hosts • X. fastidiosa has a very wide host range, with most infections remaining asymptomatic. • It seems possible that almost any plant can be a host, if associated with a xylem-sap feeding vector. • Specific combinations of hosts and X. fastidiosa genotypes result in plant disease. • Most hosts showing disease are woody perennials; fewer annual plants show symptoms. • It is currently impossible to predict the development of new diseases caused by X. fastidiosa. • Many native plant species in New Zealand can act as X. fastidiosa hosts and several are regarded as symptomatic in response to infection. • Amenity, ornamental and weed plants known to host X. -
Penetrant Adjuvant
Managing agrichemical application 100 Control of passionvine hopper and cicada eggs on kiwifruit canes with bifenthrin and a new super- penetrant adjuvant R.E. Gaskin1, D.P. Logan2, W. May3, C.A. Rowe2, K.D. Steele1, R.M. van Leeuwen1 and P.G. Connolly2 1Plant Protection Chemistry NZ, PO Box 6282, Rotorua 3043, New Zealand 2The New Zealand Institute for Plant & Food Research Limited, 412 No 1 Road, RD2, Te Puke, 3182, New Zealand 3Spray-tec, 52 Williams Rd Sth, RD3, Tauranga 3173, New Zealand Corresponding author: [email protected] Abstract A novel option for control of passionvine hopper (PVH, Scolypopa australis) and chorus cicada (Amphipsalta zelandica) on kiwifruit was investigated. This involved applying an insecticide to PVH and cicada egg sites in the dormant kiwifruit canopy, using a new type of adjuvant that allows sprays to penetrate into egg nests laid in canes and old fruit stalks. Five treatments of bifenthrin at 100 g/ha (1 litre/ha Talstar® 100EC) and preferred combinations of nozzle type, spray application volume and EngulfTM adjuvant rate were applied to dormant canes of Hayward kiwifruit in early August 2011. Water soluble blue dye added to all spray treatments penetrated into nests and stained PVH and cicada eggs when assessed shortly after application. All treatments significantly reduced hatch of PVH relative to the untreated control, by 85-99.5%. One treatment significantly reduced cicada hatch by approximately 80% relative to the control. Keywords Scolypopa australis, Amphipsalta zelandica, kiwifruit management, super- penetrant adjuvant, sooty mould. INTRODUCTION Sooty mould, which is commonly associated with target with sprays. -
View Preprint
Saving Waves: BioAcoustica Progress Report 1 Ed Baker March 2016 Abstract This report details work on the BioAcoustica project up to the end of March 2016. Functionality and datasets currently available are described and ongoing work is listed. Usage statistics are provided and future plans are presented. Outputs of the project are listed in appendices including a list of peer-reviewed papers generated by the project and peer-reviewed papers that have deposited their bioacoustic data in BioAcoustica. In ad- dition a list of species which are represented in the BioAcoustica database is provided. Contents 1 History 2 2 Current Functionality 3 2.1 Annotation . .3 2.2 Analysis . .3 2.3 bioacousticaR . .4 2.4 Collections . .4 2.5 Data Sharing . .5 2.5.1 Global Biodiversity Informatics Facility (GBIF) . .5 2.5.2 Encyclopedia of Life (EoL) . .5 3 Current Datasets 5 3.1 Global Cicada Sound Collection . .5 3.1.1 GCSC1: South Africa and Malawi . .5 3.1.2 GCSC2: Thailand . .5 3.1.3 GCSC4: Marshall et al, 2016; Lee et al, 2016 . .5 3.1.4 User Contributions . .6 3.2 Soundscapes . .6 3.3 BioAcoustica Talks . .6 3.3.1 BioAcoustica Talks Podcast . .6 3.4 3D Scans of Singing Burrows of Mole Crickets . .6 1 PeerJ Preprints | https://doi.org/10.7287/peerj.preprints.1948v2 | CC-BY 4.0 Open Access | rec: 12 Apr 2016, publ: 12 Apr 2016 EWB7 1 HISTORY 4 Usage 6 4.1 Wikipedia . .6 5 Ongoing Collections Work 7 5.1 NHM Sound Collection . .7 5.1.1 Orthoptera: Grylloidea . -
Limited, Episodic Diversification and Contrasting
Marshall et al. BMC Evolutionary Biology 2012, 12:177 http://www.biomedcentral.com/1471-2148/12/177 RESEARCH ARTICLE Open Access Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation David C Marshall1*, Kathy B R Hill1, Katharine A Marske2,3, Colleen Chambers1, Thomas R Buckley3,4,5 and Chris Simon1,6 Abstract Background: The New Zealand (NZ) cicada fauna contains two co-distributed lineages that independently colonized the isolated continental fragment in the Miocene. One extensively studied lineage includes 90% of the extant species (Kikihia + Maoricicada + Rhodopsalta; ca 51 spp.), while the other contains just four extant species (Amphipsalta – 3 spp. + Notopsalta – 1 sp.) and has been little studied. We examined mitochondrial and nuclear-gene phylogenies and phylogeography, Bayesian relaxed-clock divergence timing (incorporating literature-based uncertainty of molecular clock estimates) and ecological niche models of the species from the smaller radiation. Results: Mitochondrial and nuclear-gene trees supported the monophyly of Amphipsalta. Most interspecific diversification within Amphipsalta-Notopsalta occurred from the mid-Miocene to the Pliocene. However, interspecific divergence time estimates had large confidence intervals and were highly dependent on the assumed tree prior, and comparisons of uncorrected and patristic distances suggested difficulty in estimation of branch lengths. In contrast, intraspecific divergence times varied little across analyses, and all appear to have occurred during the Pleistocene. Two large-bodied forest taxa (A. cingulata, A. zelandica) showed minimal phylogeographic structure, with intraspecific diversification dating to ca. 0.16 and 0.37 Ma, respectively. Mid- Pleistocene-age phylogeographic structure was found within two smaller-bodied species (A.