Order Hemiptera
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Biosecurity Plan for the Vegetable Industry
Biosecurity Plan for the Vegetable Industry A shared responsibility between government and industry Version 3.0 May 2018 Plant Health AUSTRALIA Location: Level 1 1 Phipps Close DEAKIN ACT 2600 Phone: +61 2 6215 7700 Fax: +61 2 6260 4321 E-mail: [email protected] Visit our web site: www.planthealthaustralia.com.au An electronic copy of this plan is available through the email address listed above. © Plant Health Australia Limited 2018 Copyright in this publication is owned by Plant Health Australia Limited, except when content has been provided by other contributors, in which case copyright may be owned by another person. With the exception of any material protected by a trade mark, this publication is licensed under a Creative Commons Attribution-No Derivs 3.0 Australia licence. Any use of this publication, other than as authorised under this licence or copyright law, is prohibited. http://creativecommons.org/licenses/by-nd/3.0/ - This details the relevant licence conditions, including the full legal code. This licence allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to Plant Health Australia (as below). In referencing this document, the preferred citation is: Plant Health Australia Ltd (2018) Biosecurity Plan for the Vegetable Industry (Version 3.0 – 2018) Plant Health Australia, Canberra, ACT. This project has been funded by Hort Innovation, using the vegetable research and development levy and contributions from the Australian Government. Hort Innovation is the grower-owned, not for profit research and development corporation for Australian horticulture Disclaimer: The material contained in this publication is produced for general information only. -
The Influence of Prairie Restoration on Hemiptera
CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Thesis Submitted to The College of Arts and Sciences of the UNIVERSITY OF DAYTON In Partial Fulfillment of the Requirements for The Degree of Master of Science in Biology By Stephanie Kay Gunter, B.A. Dayton, Ohio August 2021 CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Name: Gunter, Stephanie Kay APPROVED BY: Chelse M. Prather, Ph.D. Faculty Advisor Associate Professor Department of Biology Ryan W. McEwan, Ph.D. Committee Member Associate Professor Department of Biology Mark G. Nielsen Ph.D. Committee Member Associate Professor Department of Biology ii © Copyright by Stephanie Kay Gunter All rights reserved 2021 iii ABSTRACT CAN THE ONE TRUE BUG BE THE ONE TRUE ANSWER? THE INFLUENCE OF PRAIRIE RESTORATION ON HEMIPTERA COMPOSITION Name: Gunter, Stephanie Kay University of Dayton Advisor: Dr. Chelse M. Prather Ohio historically hosted a patchwork of tallgrass prairies, which provided habitat for native species and prevented erosion. As these vulnerable habitats have declined in the last 200 years due to increased human land use, restorations of these ecosystems have increased, and it is important to evaluate their success. The Hemiptera (true bugs) are an abundant and varied order of insects including leafhoppers, aphids, cicadas, stink bugs, and more. They play important roles in grassland ecosystems, feeding on plant sap and providing prey to predators. Hemipteran abundance and composition can respond to grassland restorations, age of restoration, and size and isolation of habitat. -
A New Species of the Genus Euricania Melichar
Zootaxa 4033 (1): 137–143 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.4033.1.8 http://zoobank.org/urn:lsid:zoobank.org:pub:8A95CF0B-BCD9-4D34-AD74-F1C3DA4616D6 A new species of the genus Euricania Melichar, 1898 (Hemiptera: Fulgoromorpha: Ricaniidae) from China, with a world checklist and a key to all species recorded for the country LAN-LAN REN1, ADAM STROIŃSKI2 & DAO-ZHENG QIN1,* 1Key Laboratory of Plant Protection Resources and Pest Management of the Ministry of Education; Entomological Museum, North- west A&F University, Yangling, Shaanxi 712100, China 2Museum and Institute of Zoology, Polish Academy of Sciences, 64, Wilcza Street, 00-679 Warsaw, Poland 3Corresponding author. E-mail: [email protected] Abstract One new species of the planthopper genus Euricania Melichar, 1898 – E. paraclara sp. nov. is described from Guizhou (southwest China). A checklist of all Euricania species and an identification key to the species of the Chinese fauna are provided. Photographs of the adult and illustrations of male and female genitalia of the new species are also given. Key words: Fulgoroidea, planthopper, taxonomy, key, checklist Introduction The planthopper genus Euricania (Hemiptera: Ricaniidae) was established by Melichar (1898a) with the type species Pochazia ocellus Walker, 1851 designated subsequently by Distant (1906). It is a relatively large genus in the family Ricaniidae with 36 species and subspecies (Bourgoin 2015), widely distributed in the southeastern Palaearctic (China, Japan), Oriental Region (India, Bangladesh, Indonesia, Malaysia, Taiwan), New Guinea, Solomon Islands, Vanuatu, Fiji and North Australia (Fletcher 2008). -
Insects & Spiders of Kanha Tiger Reserve
Some Insects & Spiders of Kanha Tiger Reserve Some by Aniruddha Dhamorikar Insects & Spiders of Kanha Tiger Reserve Aniruddha Dhamorikar 1 2 Study of some Insect orders (Insecta) and Spiders (Arachnida: Araneae) of Kanha Tiger Reserve by The Corbett Foundation Project investigator Aniruddha Dhamorikar Expert advisors Kedar Gore Dr Amol Patwardhan Dr Ashish Tiple Declaration This report is submitted in the fulfillment of the project initiated by The Corbett Foundation under the permission received from the PCCF (Wildlife), Madhya Pradesh, Bhopal, communication code क्रम 車क/ तकनीकी-I / 386 dated January 20, 2014. Kanha Office Admin office Village Baherakhar, P.O. Nikkum 81-88, Atlanta, 8th Floor, 209, Dist Balaghat, Nariman Point, Mumbai, Madhya Pradesh 481116 Maharashtra 400021 Tel.: +91 7636290300 Tel.: +91 22 614666400 [email protected] www.corbettfoundation.org 3 Some Insects and Spiders of Kanha Tiger Reserve by Aniruddha Dhamorikar © The Corbett Foundation. 2015. All rights reserved. No part of this book may be used, reproduced, or transmitted in any form (electronic and in print) for commercial purposes. This book is meant for educational purposes only, and can be reproduced or transmitted electronically or in print with due credit to the author and the publisher. All images are © Aniruddha Dhamorikar unless otherwise mentioned. Image credits (used under Creative Commons): Amol Patwardhan: Mottled emigrant (plate 1.l) Dinesh Valke: Whirligig beetle (plate 10.h) Jeffrey W. Lotz: Kerria lacca (plate 14.o) Piotr Naskrecki, Bud bug (plate 17.e) Beatriz Moisset: Sweat bee (plate 26.h) Lindsay Condon: Mole cricket (plate 28.l) Ashish Tiple: Common hooktail (plate 29.d) Ashish Tiple: Common clubtail (plate 29.e) Aleksandr: Lacewing larva (plate 34.c) Jeff Holman: Flea (plate 35.j) Kosta Mumcuoglu: Louse (plate 35.m) Erturac: Flea (plate 35.n) Cover: Amyciaea forticeps preying on Oecophylla smargdina, with a kleptoparasitic Phorid fly sharing in the meal. -
Planthopper and Leafhopper Fauna (Hemiptera: Fulgoromorpha Et Cicadomorpha) at Selected Post-Mining Dumping Grounds in Southern Poland
Title: Planthopper and leafhopper fauna (Hemiptera: Fulgoromorpha et Cicadomorpha) at selected post-mining dumping grounds in Southern Poland Author: Marcin Walczak, Mariola Chruściel, Joanna Trela, Klaudia Sojka, Aleksander Herczek Citation style: Walczak Marcin, Chruściel Mariola, Trela Joanna, Sojka Klaudia, Herczek Aleksander. (2019). Planthopper and leafhopper fauna (Hemiptera: Fulgoromorpha et Cicadomorpha) at selected post-mining dumping grounds in Southern Poland. “Annals of the Upper Silesian Museum in Bytom, Entomology” Vol. 28 (2019), s. 1-28, doi 10.5281/zenodo.3564181 ANNALS OF THE UPPER SILESIAN MUSEUM IN BYTOM ENTOMOLOGY Vol. 28 (online 006): 1–28 ISSN 0867-1966, eISSN 2544-039X (online) Bytom, 05.12.2019 MARCIN WALCZAK1 , Mariola ChruśCiel2 , Joanna Trela3 , KLAUDIA SOJKA4 , aleksander herCzek5 Planthopper and leafhopper fauna (Hemiptera: Fulgoromorpha et Cicadomorpha) at selected post- mining dumping grounds in Southern Poland http://doi.org/10.5281/zenodo.3564181 Faculty of Natural Sciences, University of Silesia, Bankowa Str. 9, 40-007 Katowice, Poland 1 e-mail: [email protected]; 2 [email protected]; 3 [email protected] (corresponding author); 4 [email protected]; 5 [email protected] Abstract: The paper presents the results of the study on species diversity and characteristics of planthopper and leafhopper fauna (Hemiptera: Fulgoromorpha et Cicadomorpha) inhabiting selected post-mining dumping grounds in Mysłowice in Southern Poland. The research was conducted in 2014 on several sites located on waste heaps with various levels of insolation and humidity. During the study 79 species were collected. The paper presents the results of ecological analyses complemented by a qualitative analysis performed based on the indices of species diversity. -
A New Pupillarial Scale Insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in Coastal New South Wales, Australia
Zootaxa 4117 (1): 085–100 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4117.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:5C240849-6842-44B0-AD9F-DFB25038B675 A new pupillarial scale insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in coastal New South Wales, Australia PENNY J. GULLAN1,3 & DOUGLAS J. WILLIAMS2 1Division of Evolution, Ecology & Genetics, Research School of Biology, The Australian National University, Acton, Canberra, A.C.T. 2601, Australia 2The Natural History Museum, Department of Life Sciences (Entomology), London SW7 5BD, UK 3Corresponding author. E-mail: [email protected] Abstract A new scale insect, Aolacoccus angophorae gen. nov. and sp. nov. (Eriococcidae), is described from the bark of Ango- phora (Myrtaceae) growing in the Sydney area of New South Wales, Australia. These insects do not produce honeydew, are not ant-tended and probably feed on cortical parenchyma. The adult female is pupillarial as it is retained within the cuticle of the penultimate (second) instar. The crawlers (mobile first-instar nymphs) emerge via a flap or operculum at the posterior end of the abdomen of the second-instar exuviae. The adult and second-instar females, second-instar male and first-instar nymph, as well as salient features of the apterous adult male, are described and illustrated. The adult female of this new taxon has some morphological similarities to females of the non-pupillarial palm scale Phoenicococcus marlatti Cockerell (Phoenicococcidae), the pupillarial palm scales (Halimococcidae) and some pupillarial genera of armoured scales (Diaspididae), but is related to other Australian Myrtaceae-feeding eriococcids. -
Hemiptera: first Record for an Australian Lophopid (Hemiptera, Lophopidae)
Australian Journal of Entomology (2007) 46, 129–132 Historical use of substrate-borne acoustic production within the Hemiptera: first record for an Australian Lophopid (Hemiptera, Lophopidae) Adeline Soulier-Perkins,1* Jérôme Sueur2 and Hannelore Hoch3 1Muséum National d’Histoire Naturelle, Département Systématique et Évolution, USM 601 MNHN & UMR 5202 CNRS, Case Postale 50, 45, Rue Buffon, F-75005 Paris, France. 2NAMC-CNRS UMR 8620, Bât. 446, Université Paris XI, F-91405 Orsay Cedex, France. 3Museum für Naturkunde, Institut für Systematische Zoologie, Humboldt-Universität zu Berlin Invalidenstr. 43, D- 10115 Berlin, Germany. Abstract Here the first record of communication through substrate-borne vibrations for the Lophopidae family is reported. The signals from Magia subocellata that the authors recorded were short calls with a decreasing frequency modulation. Acoustic vibrations have been observed for other families within the Hemiptera and a scenario concerning the historical use of vibrational communication within the Hemiptera is tested using a phylogenetic inference. The most parsimonious hypothesis suggests that substrate-borne communication is ancestral for the hemipteran order and highlights the groups for which future acoustic research should be undertaken. Key words Cicadomorpha, Coleorrhyncha, evolutionary scenario, Heteroptera, Sternorrhyncha, substrate vibration. INTRODUCTION Lophopidae migrating into America via the Bering land bridge. Some other ancestors of the extant groups moved onto Many animals have been recently recognised for their ability newly emerging land in the Pacific, expanding their distribu- to communicate through substrate-borne vibrations (Hill tion as far east as the Samoan Islands, and as far south as 2001). While elephants produce vibrations transmitted by the Australia (Soulier-Perkins 2000). -
Melon Aphid Or Cotton Aphid, Aphis Gossypii Glover (Insecta: Hemiptera: Aphididae)1 John L
EENY-173 Melon Aphid or Cotton Aphid, Aphis gossypii Glover (Insecta: Hemiptera: Aphididae)1 John L. Capinera2 Distribution generation can be completed parthenogenetically in about seven days. Melon aphid occurs in tropical and temperate regions throughout the world except northernmost areas. In the In the south, and at least as far north as Arkansas, sexual United States, it is regularly a pest in the southeast and forms are not important. Females continue to produce southwest, but is occasionally damaging everywhere. Be- offspring without mating so long as weather allows feeding cause melon aphid sometimes overwinters in greenhouses, and growth. Unlike many aphid species, melon aphid is and may be introduced into the field with transplants in the not adversely affected by hot weather. Melon aphid can spring, it has potential to be damaging almost anywhere. complete its development and reproduce in as little as a week, so numerous generations are possible under suitable Life Cycle and Description environmental conditions. The life cycle differs greatly between north and south. In the north, female nymphs hatch from eggs in the spring on Egg the primary hosts. They may feed, mature, and reproduce When first deposited, the eggs are yellow, but they soon parthenogenetically (viviparously) on this host all summer, become shiny black in color. As noted previously, the eggs or they may produce winged females that disperse to normally are deposited on catalpa and rose of sharon. secondary hosts and form new colonies. The dispersants typically select new growth to feed upon, and may produce Nymph both winged (alate) and wingless (apterous) female The nymphs vary in color from tan to gray or green, and offspring. -
Insects and Molluscs, According to the Procedures Outlined Below
Bush Blitz – ACT Expedition 26 Nov – 6 Dec 2018 ACT Expedition Bush Blitz Hemiptera, Hymenoptera, Lepidoptera, Orthoptera, Terrestrial molluscs 26 Nov – 6 Dec 2018 Submitted: 5 April 2019 Debbie Jennings and Olivia Evangelista 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 43 Bush Blitz – ACT Expedition 26 Nov – 6 Dec 2018 Contents Contents .................................................................................................................................. 2 List of contributors ................................................................................................................... 3 Abstract ................................................................................................................................... 4 1. Introduction ...................................................................................................................... 4 2. Methods .......................................................................................................................... 6 2.1 Site selection ............................................................................................................. 6 2.2 Survey techniques ..................................................................................................... 6 2.2.1 Methods used at standard survey sites ................................................................... 7 2.3 Identifying -
Saprophylic Hemiptera Roth Complete
Saproxylic Hemiptera Taxonomy, Ecology & Evolu8on Steffen Roth, University Museum Bergen, Norway Воро́неж, 26 ию́ нь 2019 г. Outline: Hemiptera? What the f*** is a bug? Which taxa do we find in dead wood? Morphological and physiological adapta?on Evolu?on of saproxylic Hemiptera and how to entangle it: a case study An ecological case study: What aCracts saproxylic Hemiptera towards dead wood? scale insects jumping plant lice Aphids White flies cicadas scale insects Homoptera s.stricto spi:le bugs leaf hopper tree hopper Cicadinea Planthoppers thorn bugs Fulgoridae lanternflies Derbidae Fla-dae Delphacidae moss bugs Malcolm Burrows et al. J Exp Biol 2007;210:3311-3318 moss bugs true bugs Kevin P. Johnson et al. PNAS 2018;115:50:12775-12780 Gosner & Damken 2018 Saproxylic hemiptera- feeding types Several Families of Heteroptera Aradidae (flat bugs), 1800 spp.: - 90% of all spp. fungi feeder - all live stages Reduviidae (Assassin bug), 6800 spp.: - predators Miridae (plant bugs), 10 000 spp.: - all feeding types - only 1 of 7 subfamilies strictly saproxylic (Cylapinae: ca 50 spp.) Fulgoromorpha: - Fungi feeder and predators, oJen - Achilidae and Derbidae (out of 21 unknown families) -only nymphs are saproxylic Anthocoridae (minute pirate/flower bugs), 600 spp: - all feeding types - host plant specific among predatory spp. Morphological and physiological adapta1on 1 - extremely dorsoventrally fla9ened body - waxy surface - special secretory glands and gut structure for myceto-phagous feeding - Elonga1on of stylet bundles Morphological and physiological adapta,on 2 - wing reduc,on/losses (50% of all known genera and most subfamilies od Aradidae) - camouflaged in their habitat: colour and tubercular bark mimics - acyclic reproduc,on Morphological and physiological adaptation 3 - Piryphilous and secondary colonization of burned forest - photomechanic infrared sensilla * Aradus angularis Gossner et al. -
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ISSN 1994-4136 (print) ISSN 1997-3500 (online) Myrmecological News Volume 26 February 2018 Schriftleitung / editors Florian M. STEINER, Herbert ZETTEL & Birgit C. SCHLICK-STEINER Fachredakteure / subject editors Jens DAUBER, Falko P. DRIJFHOUT, Evan ECONOMO, Heike FELDHAAR, Nicholas J. GOTELLI, Heikki O. HELANTERÄ, Daniel J.C. KRONAUER, John S. LAPOLLA, Philip J. LESTER, Timothy A. LINKSVAYER, Alexander S. MIKHEYEV, Ivette PERFECTO, Christian RABELING, Bernhard RONACHER, Helge SCHLÜNS, Chris R. SMITH, Andrew V. SUAREZ Wissenschaftliche Beratung / editorial advisory board Barry BOLTON, Jacobus J. BOOMSMA, Alfred BUSCHINGER, Daniel CHERIX, Jacques H.C. DELABIE, Katsuyuki EGUCHI, Xavier ESPADALER, Bert HÖLLDOBLER, Ajay NARENDRA, Zhanna REZNIKOVA, Michael J. SAMWAYS, Bernhard SEIFERT, Philip S. WARD Eigentümer, Herausgeber, Verleger / publisher © 2018 Österreichische Gesellschaft für Entomofaunistik c/o Naturhistorisches Museum Wien, Burgring 7, 1010 Wien, Österreich (Austria) Myrmecological News 26 31-45 Vienna, February 2018 How common is trophobiosis with hoppers (Hemi ptera: Auchenorrhyncha) inside ant nests (Hymeno ptera: Formicidae)? Novel interactions from New Guinea and a worldwide overview Petr KLIMES, Michaela BOROVANSKA, Nichola S. PLOWMAN & Maurice LEPONCE Abstract Trophobiotic interactions between ants and honeydew-providing hemi pterans are widespread and are one of the key mechanisms that maintain ant super-abundance in ecosystems. Many of them occur inside ant nests. However, these cryptic associations are poorly understood, particularly those with hoppers (suborder Auchenorrhyncha). Here, we study tree-dwelling ant and Hemi ptera communities in nests along the Mt. Wilhelm elevational gradient in Papua New Guinea and report a new case of this symbiosis between Pseudolasius EMERY, 1887 ants and planthoppers. Fur- thermore, we provide a worldwide review of other ant-hopper interactions inside ant-built structures and compare their nature (obligate versus facultative) and distribution within the suborder Auchenorrhyncha. -
Diversity and Abundance of Insect Herbivores Foraging on Seedlings in a Rainforest in Guyana
R Ecological Entomology (1999) 24, 245±259 Diversity and abundance of insect herbivores foraging on seedlings in a rainforest in Guyana YVES BASSET CABI Bioscience: Environment, Ascot, U.K. Abstract. 1. Free-living insect herbivores foraging on 10 000 tagged seedlings representing ®ve species of common rainforest trees were surveyed monthly for more than 1 year in an unlogged forest plot of 1 km2 in Guyana. 2. Overall, 9056 insect specimens were collected. Most were sap-sucking insects, which represented at least 244 species belonging to 25 families. Leaf-chewing insects included at least 101 species belonging to 16 families. Herbivore densities were among the lowest densities reported in tropical rainforests to date: 2.4 individuals per square metre of foliage. 3. Insect host speci®city was assessed by calculating Lloyd's index of patchiness from distributional records and considering feeding records in captivity and in situ. Generalists represented 84 and 78% of sap-sucking species and individuals, and 75 and 42% of leaf-chewing species and individuals. In particular, several species of polyphagous xylem-feeding Cicadellinae were strikingly abundant on all hosts. 4. The high incidence of generalist insects suggests that the Janzen±Connell model, explaining rates of attack on seedlings as a density-dependent process resulting from contagion of specialist insects from parent trees, is unlikely to be valid in this study system. 5. Given the rarity of ¯ushing events for the seedlings during the study period, the low insect densities, and the high proportion of generalists, the data also suggest that seedlings may represent a poor resource for free-living insect herbivores in rainforests.