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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. -
Elytra Reduction May Affect the Evolution of Beetle Hind Wings
Zoomorphology https://doi.org/10.1007/s00435-017-0388-1 ORIGINAL PAPER Elytra reduction may affect the evolution of beetle hind wings Jakub Goczał1 · Robert Rossa1 · Adam Tofilski2 Received: 21 July 2017 / Revised: 31 October 2017 / Accepted: 14 November 2017 © The Author(s) 2017. This article is an open access publication Abstract Beetles are one of the largest and most diverse groups of animals in the world. Conversion of forewings into hardened shields is perceived as a key adaptation that has greatly supported the evolutionary success of this taxa. Beetle elytra play an essential role: they minimize the influence of unfavorable external factors and protect insects against predators. Therefore, it is particularly interesting why some beetles have reduced their shields. This rare phenomenon is called brachelytry and its evolution and implications remain largely unexplored. In this paper, we focused on rare group of brachelytrous beetles with exposed hind wings. We have investigated whether the elytra loss in different beetle taxa is accompanied with the hind wing shape modification, and whether these changes are similar among unrelated beetle taxa. We found that hind wings shape differ markedly between related brachelytrous and macroelytrous beetles. Moreover, we revealed that modifications of hind wings have followed similar patterns and resulted in homoplasy in this trait among some unrelated groups of wing-exposed brachelytrous beetles. Our results suggest that elytra reduction may affect the evolution of beetle hind wings. Keywords Beetle · Elytra · Evolution · Wings · Homoplasy · Brachelytry Introduction same mechanism determines wing modification in all other insects, including beetles. However, recent studies have The Coleoptera order encompasses almost the quarter of all provided evidence that formation of elytra in beetles is less currently known animal species (Grimaldi and Engel 2005; affected by Hox gene than previously expected (Tomoyasu Hunt et al. -
Wetlands Resource Has Been Developed to Encourage You and Your Class to Visit Wetlands in Your ‘Backyard’
WETLANDS for Education in the West Coast Tai Poutini Conservancy January 2005 Edition 2 WETLANDS for Education in the West Coast Tai Poutini Conservancy ACKNOWLEDGEMENTS A large number of people have been involved in the production and editing of this resource. We would like to thank them all and in particular the following: Area and Conservancy staff, especially Philippe Gerbeaux for their comments and assistance. Te Rüanga o Ngäi Tahu, Te Rünaka o Makäwhio and Te Rünaka o Ngäti Waewae for their comments and assistance through Rob Tipa. Compiled by Chrisie Sargent, Sharleen Hole and Kate Leggett Edited by Sharleen Hole and Julie Dutoit Illustrations by Sue Asplin ISBN 0-478-22656-X 2nd Edition January 2005 Published by: Department of Conservation Greymouth Mawheranui Area Office PO Box 370 Greymouth April 2004 CONTENTS USING THIS RESOURCE 5 THE CURRICULUM 5 WHY WETLANDS? 8 RAMSAR CONVENTION 9 SAFETY 9 BE PREPARED ACTIVITY 10 PRE VISIT ACTIVITIES 11 POST VISIT ACTIVITIES 12 FACT SHEETS What is a wetland? 15 Types of wetlands 17 How wetlands change over time 19 Threats to wetlands 21 Wetland uses & users 23 The water cycle is important for wetlands 24 Catchments 25 Water quality 27 Invertebrates 29 Wetland soils 30 Did you know that coal formed from swamps? 31 Wetland plants 32 Wetland fish 33 Whitebait-what are they? 34 Wetland birds 35 Food chains & food webs 37 Wetlands - a 'supermarket' for tai poutini maori 39 ACTIVITY SHEETS Activity 1: What is . a wetland? 43 Activity 2: What is . a swamp? 44 Activity 3: What is . an estuary? 45 Activity 4: What is . -
Read the Decision
Decision Date 5 February 2021 Application number APP203875 Application type To import for release and/or release from containment any new organism under section 34 of the Hazardous Substances and New Organisms Act 1996 Applicant Tasman District Council Date of hearing/consideration 17 December 2020 Date Application received 14 September 2020 Considered by A decision-making committee of the Environmental Protection Authority (the Committee)1 Dr Nick Roskruge (Chair) Dr John Taylor Mr Peter Cressey Purpose of the application To import and release two parasitoids, Metoecus paradoxus and Volucella inanis as biological control agents for the invasive German and common wasps (Vespula germanica and V. vulgaris). New organism approved Metoecus paradoxus Linnaeus 1761 Volucella inanis Linnaeus 1758 1 The Committee referred to in this decision is the subcommittee that has made the decision on this application under delegated authority in accordance with section 18A of the Act. Decision APP203875 Summary of decision 1. Application APP203875 to import and release two parasitoids, Metoecus paradoxus and Volucella inanis, as biological control agents (BCAs) for the invasive German and common wasps (Vespula germanica and V. vulgaris), in New Zealand, was lodged under section 34 of the Hazardous Substances and New Organisms Act 1996 (the Act). 2. The application was considered in accordance with the relevant provisions of the Act and of the HSNO (Methodology) Order 1998 (the Methodology). 3. The Committee has approved the application in accordance with section 38(1)(a) of the Act. Application and consideration process 4. The application was formally received on 14 September 2020. 5. The applicant, Tasman District Council, applied to the Environmental Protection Authority (EPA) to import and release two parasitoids, Metoecus paradoxus and Volucella inanis, as BCAs for the invasive German and common wasps (Vespula germanica and V. -
The Major Genetic Features of the Order Odonata Are Well Known (Cf
Odonalologica 9(1): 29 JJ March /. 1980 The karyotypes of five species of Odonataendemic to New Zealand A.L. Jensen¹ Zoology Department, University of Canterbury, Christchurch-I, New Zealand Received April 10, 1979 The chromosome = 4 formula, n <5 13 (X. hi), characterises spp.: Austrolestes colensonis (White) (Lestidae), Uropetala carovei (White) (Petaluridae), Procordulia grayi (Sel.) and P. smithii (White) (Corduliidae). The karyotype of is 14 Xanthomemis zelandica (McLach.) (Coenagrionidae) described by n <J= (X). Save U. carovei of these have been far. for none spp. examined cytologically so INTRODUCTION The major genetic features of the Order Odonata are well known (cf. for example KIAUTA, 1972). The karyotypes ofalmost 500 species, representing 20 of the 27 existent families, have been determined. However, most of these records refer to Northern Hemisphere species and little cytological information is available from Australasia. Cytological studies of the many endemic species occurring in both Australia and New Zealand will therefore aid the development of a complete cytophylogenetic picture of the Order, and may also help to indicatethe relationships ofthesespecies with the world fauna. Of the II Odonata species present in New Zealand, six are endemic. of five endemic in Karyotypes the species known to occur Mid Canterbury, South Island (cf. CROSBY, DUGDALE& WATT, 1976)are presented here. MATERIAL AND METHODS and males collected Isaac's Pond Larval, teneral, mature were from (43°28’S. 172° 32'E)and/ or 0 Lake Sarah (43°03'S. 171 47’E). The testes were removed and fixed in 3; I absolutealcohohglacial 1 Present address: c o K. Andersen, Ludvig Jensensvej 3. -
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). -
Spiders 27 November-5 December 2018 Submitted: August 2019 Robert Raven
Bush Blitz – Namadgi, ACT 27 Nov-5 Dec 2018 Namadgi, ACT Bush Blitz Spiders 27 November-5 December 2018 Submitted: August 2019 Robert Raven Nomenclature and taxonomy used in this report is consistent with: The Australian Faunal Directory (AFD) http://www.environment.gov.au/biodiversity/abrs/online-resources/fauna/afd/home Page 1 of 12 Bush Blitz – Namadgi, ACT 27 Nov-5 Dec 2018 Contents Contents .................................................................................................................................. 2 List of contributors ................................................................................................................... 2 Abstract ................................................................................................................................... 4 1. Introduction ...................................................................................................................... 4 2. Methods .......................................................................................................................... 4 2.1 Site selection ............................................................................................................. 4 2.2 Survey techniques ..................................................................................................... 4 2.2.1 Methods used at standard survey sites ................................................................... 5 2.3 Identifying the collections ......................................................................................... -
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. -
Myrmarachnine Jumping Spiders of the New Subtribe Levieina from Papua
A peer-reviewed open-access journal ZooKeys 842: 85–112 (2019) New myrmarachnine jumping spiders 85 doi: 10.3897/zookeys.842.32970 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Myrmarachnine jumping spiders of the new subtribe Levieina from Papua New Guinea (Araneae, Salticidae, Myrmarachnini) Wayne P. Maddison1, Tamás Szűts2 1 Departments of Zoology and Botany and Beaty Biodiversity Museum, University of British Columbia, 6270 University Boulevard, Vancouver, British Columbia, V6T 1Z4, Canada 2 Department of Ecology, University of Veterinary Medicine Budapest, Budapest, H1077, Rottenbiller u. 50, Hungary Corresponding author: Wayne P. Maddison (wayne.maddison@ ubc.ca) Academic editor: Jeremy Miller | Received 10 January 2019 | Accepted 12 March 2019 | Published 7 May 2019 http://zoobank.org/D911C055-FF4B-4900-877B-123951761AC1 Citation: Maddison WP, Szűts T (2019) Myrmarachnine jumping spiders of the new subtribe Levieina from Papua New Guinea (Araneae, Salticidae, Myrmarachnini). ZooKeys 842: 85–112. https://doi.org/10.3897/zookeys.842.32970 Abstract A previously unreported radiation of myrmarachnine jumping spiders from New Guinea is described, which, although having few known species, is remarkably diverse in body forms. This clade is the new subtribe Levieina, represented by seven new species in three new genera. Within Leviea gen. n. are three new species, L. herberti sp. n., L. lornae sp. n., and L. francesae sp. n., all of which are unusual among the myrmarachnines in appearing as typical salticids, not antlike. Papuamyr gen. n. superficially resembles Ligonipes Karsch, 1878 or Rhombonotus L. Koch, 1879 as a compact antlike spider, but lacks their laterally- compressed palp and bears an ectal spur on the paturon of the chelicera. -
Abstract Book Revised 25 June
ABSTRACT BOOK ASSAB Waiheke, Auckland 8-10 July 2019 NAU MAI - WELCOME Pg. 3 ASSAB CODE OF CONDUCT Pg. 4 PROGRAMME Pg. 6 KEYNOTE SPEAKERS Pg. 10 ORAL PRESENTATIONS Pg. 18 POSTERS Pg. 75 HAERE MAI – FAREWELL Pg. 97 2 NAU MAI, HAERE MAI KI WAIHEKE! We warmly welcome you to Waiheke. We hope you will enjoy meeting the people, nature and land of Tāmaki Makaurau/Auckland. At ASSAB 2019 we aim to celebrate diversity in all its forms – diverse people, nature, research and scholarly approaches. We thank the Waiheke Island community including the Piritahi Marae committee, for their support. We respect and recognise Ngati Paoa as mana whenua and the interests of the wider Pare Hauraki iwi. Ruia kupu KĀEA: RuIa KATOA: Ruia ngā kākano i te Moananui- Scatter and sow the seeds across the Pacific ā-Kiwa wherahia ki te moana rongonui Spread forth to the famous body of water Herea ngā waka ki te pou whakairo Tether the canoes to the pou whakairo ka tū ki Waitematā Standing in the Waitematā I raro i te marumaru o ngā maunga tapu Beneath the shade of the sacred mountains; Ko Waipapa te manawa whenua Waipapa is the heartbeat o te whare wānanga nei of this University M. Steedman, Te Whare Wānanga o Tāmaki Makaurau, Aotearoa/ University of Auckland, New Zealand TūtIra maI www.youtube.com/watch?v=klLSVac79Zk or https://www.youtube.com/watch?v=VxorRtINRTc Tūtira mai ngā iwi Line up together, people Tātou tātou e All of us, all of us. Tūtira mai ngā iwi Line up together, people Tātou tātou e All of us, all of us. -
Encyclopedia of Social Insects
G Guests of Social Insects resources and homeostatic conditions. At the same time, successful adaptation to the inner envi- Thomas Parmentier ronment shields them from many predators that Terrestrial Ecology Unit (TEREC), Department of cannot penetrate this hostile space. Social insect Biology, Ghent University, Ghent, Belgium associates are generally known as their guests Laboratory of Socioecology and Socioevolution, or inquilines (Lat. inquilinus: tenant, lodger). KU Leuven, Leuven, Belgium Most such guests live permanently in the host’s Research Unit of Environmental and nest, while some also spend a part of their life Evolutionary Biology, Namur Institute of cycle outside of it. Guests are typically arthropods Complex Systems, and Institute of Life, Earth, associated with one of the four groups of eusocial and the Environment, University of Namur, insects. They are referred to as myrmecophiles Namur, Belgium or ant guests, termitophiles, melittophiles or bee guests, and sphecophiles or wasp guests. The term “myrmecophile” can also be used in a broad sense Synonyms to characterize any organism that depends on ants, including some bacteria, fungi, plants, aphids, Inquilines; Myrmecophiles; Nest parasites; and even birds. It is used here in the narrow Symbionts; Termitophiles sense of arthropods that associated closely with ant nests. Social insect nests may also be parasit- Social insect nests provide a rich microhabitat, ized by other social insects, commonly known as often lavishly endowed with long-lasting social parasites. Although some strategies (mainly resources, such as brood, retrieved or cultivated chemical deception) are similar, the guests of food, and nutrient-rich refuse. Moreover, nest social insects and social parasites greatly differ temperature and humidity are often strictly regu- in terms of their biology, host interaction, host lated. -
Here Damselflies, on the Other Hand, Look Else in the World
Contents Preface vii Natural History Damselflies and dragonflies in the natural world 1 Habitats of New Zealand damselflies and dragonflies 4 Endemics and more recent arrivals 9 Biology and behaviour 12 Conservation 51 Photographing damselflies and dragonflies 54 Damselflies, dragonflies and communities 56 Species Accounts Blue damselfly Austrolestes colensonis 60 Gossamer damselfly Ischnura aurora 66 Chatham redcoat damselfly Xanthocnemis tuanuii 72 Redcoat damselfly Xanthocnemis zealandica 78 Bush giant dragonfly Uropetala carovei 84 Mountain giant dragonfly Uropetala chiltoni 90 Lancer dragonfly Aeshna brevistyla 96 Baron dragonfly Anax papuensis 102 Dusk dragonfly Antipodochlora braueri 108 Sentry dragonfly Hemicordulia australiae 114 Yellow spotted dragonfly ‘Procordulia’ grayi 120 Ranger dragonfly Procordulia smithii 126 Red percher dragonfly Diplacodes bipunctata 132 Common glider dragonfly Tramea loewii 138 Species Likely to Establish 144 Bibliography 148 Acknowledgements 151 A teneral sentry dragonfly clings to its exuvia while hardening through the night. Preface Dragonflies – if a name should reflect The New Zealand damselfly and character, then dragonflies could not have dragonfly fauna comprises 14 species been better named. Dragons in legends, currently known to breed in the North and mythologies and fairy tales are often South Islands, Stewart Island/Rakiura and pictured as strong, fearsome, merciless the Chatham Islands. Additional species rulers of the air, but are sometimes have been recorded on the Kermadec portrayed as full of wisdom. Dragonflies Islands and others still have arrived have it all: they are strong, dynamic fliers occasionally on New Zealand’s main islands showing no mercy towards mosquitoes but have failed to establish permanent or many other small insects. What about populations.