Endosymbiotic Microorganisms of Scale Insects
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Based on Comparative Morphological Data AF Emel'yanov Transactions of T
The phylogeny of the Cicadina (Homoptera, Cicadina) based on comparative morphological data A.F. Emel’yanov Transactions of the All-Union Entomological Society Morphological principles of insect phylogeny The phylogenetic relationships of the principal groups of cicadine* insects have been considered on more than one occasion, commencing with Osborn (1895). Some phylogenetic schemes have been based only on data relating to contemporary cicadines, i.e. predominantly on comparative morphological data (Kirkaldy, 1910; Pruthi, 1925; Spooner, 1939; Kramer, 1950; Evans, 1963; Qadri, 1967; Hamilton, 1981; Savinov, 1984a), while others have been constructed with consideration given to paleontological material (Handlirsch, 1908; Tillyard, 1919; Shcherbakov, 1984). As the most primitive group of the cicadines have been considered either the Fulgoroidea (Kirkaldy, 1910; Evans, 1963), mainly because they possess a small clypeus, or the cicadas (Osborn, 1895; Savinov, 1984), mainly because they do not jump. In some schemes even the monophyletism of the cicadines has been denied (Handlirsch, 1908; Pruthi, 1925; Spooner, 1939; Hamilton, 1981), or more precisely in these schemes the Sternorrhyncha were entirely or partially depicted between the Fulgoroidea and the other cicadines. In such schemes in which the Fulgoroidea were accepted as an independent group, among the remaining cicadines the cicadas were depicted as branching out first (Kirkaldy, 1910; Hamilton, 1981; Savinov, 1984a), while the Cercopoidea and Cicadelloidea separated out last, and in the most widely acknowledged systematic scheme of Evans (1946b**) the last two superfamilies, as the Cicadellomorpha, were contrasted to the Cicadomorpha and the Fulgoromorpha. At the present time, however, the view affirming the equivalence of the four contemporary superfamilies and the absence of a closer relationship between the Cercopoidea and Cicadelloidea (Evans, 1963; Emel’yanov, 1977) is gaining ground. -
Correlation of Stylet Activities by the Glassy-Winged Sharpshooter, Homalodisca Coagulata (Say), with Electrical Penetration Graph (EPG) Waveforms
ARTICLE IN PRESS Journal of Insect Physiology 52 (2006) 327–337 www.elsevier.com/locate/jinsphys Correlation of stylet activities by the glassy-winged sharpshooter, Homalodisca coagulata (Say), with electrical penetration graph (EPG) waveforms P. Houston Joosta, Elaine A. Backusb,Ã, David Morganc, Fengming Yand aDepartment of Entomology, University of Riverside, Riverside, CA 92521, USA bUSDA-ARS Crop Diseases, Pests and Genetics Research Unit, San Joaquin Valley Agricultural Sciences Center, 9611 South Riverbend Ave, Parlier, CA 93648, USA cCalifornia Department of Food and Agriculture, Mt. Rubidoux Field Station, 4500 Glenwood Dr., Bldg. E, Riverside, CA 92501, USA dCollege of Life Sciences, Peking Univerisity, Beijing, China Received 5 May 2005; received in revised form 29 November 2005; accepted 29 November 2005 Abstract Glassy-winged sharpshooter, Homalodisca coagulata (Say), is an efficient vector of Xylella fastidiosa (Xf), the causal bacterium of Pierce’s disease, and leaf scorch in almond and oleander. Acquisition and inoculation of Xf occur sometime during the process of stylet penetration into the plant. That process is most rigorously studied via electrical penetration graph (EPG) monitoring of insect feeding. This study provides part of the crucial biological meanings that define the waveforms of each new insect species recorded by EPG. By synchronizing AC EPG waveforms with high-magnification video of H. coagulata stylet penetration in artifical diet, we correlated stylet activities with three previously described EPG pathway waveforms, A1, B1 and B2, as well as one ingestion waveform, C. Waveform A1 occured at the beginning of stylet penetration. This waveform was correlated with salivary sheath trunk formation, repetitive stylet movements involving retraction of both maxillary stylets and one mandibular stylet, extension of the stylet fascicle, and the fluttering-like movements of the maxillary stylet tips. -
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. -
A New Family of Coreoidea from the Lower Cretaceous Lebanese Amber (Hemiptera: Pentatomomorpha)
P O L I S H JOUR NAL OF ENTOMOLO G Y POLSKIE PISMO ENTOMOL OGICZ N E VOL. 80: 627-644 Gdynia 31 December 2011 DOI: 10.2478/v10200-011-0049-5 A new family of Coreoidea from the Lower Cretaceous Lebanese Amber (Hemiptera: Pentatomomorpha) DANY AZAR1, ANDRÉ NEL2, MICHAEL S. ENGEL3, 4, ROMAIN GARROUSTE2, ARMAND MATOCQ2 1Lebanese University, Faculty of Sciences II, Department of Natural Sciences, PO box 26110217, Fanar – Matn, Lebanon, e-mail: [email protected]; 2CNRS UMR 7205, CP 50, Entomologie, Muséum National d'Histoire Naturelle, 45 rue Buffon, F-75005 Paris, France, e-mails: [email protected], [email protected], [email protected]; 3Division of Entomology (Paleoentomology), Natural History Museum, University of Kansas, Lawrence, KS 66049-2811, USA, e-mail: [email protected]; 4Department of Ecology & Evolutionary Biology, 1501 Crestline Drive – Suite 140, University of Kansas, Lawrence, KS 66049-2811, USA ABSTRACT. A new genus and species, Yuripopovina magnifica, belonging to a new coreoid family, Yuripopovinidae (Hemiptera: Pentatomomorpha), is described and illustrated from the Lower Cretaceous amber of Lebanon. The species represents the first definitive Mesozoic record for the Coreoidea. A cladistic analysis of Coreoidea, including the new family, is undertaken. KEY WORDS: Pentatomomorpha, Coreoidea, Yuripopovinidae, fam. n., gen. n., sp. n., Lebanon, phylogeny. INTRODUCTION The Pentatomomorpha with its 14 000 known living species (WEIRAUCH & SCHUH 2011) is the second largest of the seven heteropteran infraorders (SCHAEFER 1993, ŠTYS & KERZHNER 1975) (Enicocephalomorpha, Dipsocoromorpha, Gerromorpha, Nepomorpha, Leptodomorpha, Cimicomorpha, and Pentatomorpha). Most authors recognize five superfamilies within Pentatomomorpha, but there remains controversy regarding the 628 Polish Journal of Entomology 80 (4) composition of these superfamilies (SCHAEFER 1993, ŠTYS 1961). -
Environment Vs Mode Horizontal Mixed Vertical Aquatic 34 28 6 Terrestrial 36 122 215
environment vs mode horizontal mixed vertical aquatic 34 28 6 terrestrial 36 122 215 route vs mode mixed vertical external 54 40 internal 96 181 function vs mode horizontal mixed vertical nutrition 60 53 128 defense 1 33 15 multicomponent 0 9 8 unknown 9 32 70 manipulation 0 23 0 host classes vs symbiosis factors horizontal mixed vertical na external internal aquatic terrestrial nutrition defense multiple factor unknown manipulation Arachnida 0 0 2 0 0 2 0 2 2 0 0 0 0 Bivalvia 19 13 2 19 0 15 34 0 34 0 0 0 0 Bryopsida 2 0 0 2 0 0 0 2 2 0 0 0 0 Bryozoa 0 1 0 0 0 1 1 0 0 1 0 0 0 Cephalopoda 1 0 0 1 0 0 1 0 0 1 0 0 0 Chordata 0 1 0 0 1 0 1 0 1 0 0 0 0 Chromadorea 0 2 0 0 2 0 2 0 2 0 0 0 0 Demospongiae 1 2 0 1 0 2 3 0 0 0 0 3 0 Filicopsida 0 2 0 0 0 2 0 2 2 0 0 0 0 Gastropoda 5 0 0 5 0 0 5 0 5 0 0 0 0 Hepaticopsida 4 0 0 4 0 0 0 4 4 0 0 0 0 Homoscleromorpha 0 1 0 0 0 1 1 0 0 0 0 1 0 Insecta 8 112 208 8 82 238 3 325 151 43 9 105 20 Liliopsida 4 0 0 4 0 0 0 4 4 0 0 0 0 Magnoliopsida 17 4 0 17 0 4 0 21 17 4 0 0 0 Malacostraca 2 2 0 2 0 2 3 1 2 0 0 0 2 Maxillopoda 0 1 0 0 0 1 1 0 0 0 0 0 1 Nematoda 0 1 1 0 1 1 0 2 0 0 1 1 0 Oligochaeta 0 8 0 0 8 0 6 2 7 0 0 1 0 Polychaeta 6 0 0 6 0 0 6 0 6 0 0 0 0 Secernentea 0 0 7 0 0 7 0 7 0 0 7 0 0 Sphagnopsida 1 0 0 1 0 0 0 1 1 0 0 0 0 Turbellaria 0 0 1 0 0 1 1 0 1 0 0 0 0 host families vs. -
From Museum Specimen Database to Ecological Statement
From Museum Specimen Database to Ecological Statement Christine A. Johnson1, Richard K. Rabeler2, Charles Bartlett3 © Tom Murray @Rob Naczi © Tom Murray 2 1 3 SPNHC – Cardiff - 2014 Tri-trophic Digitization Thematic Collections Network PI: Randall“Toby” Schuh (AMNH) 32 institutions: 18 insect collections, 14 herbaria NYBG is lead on botanical digitization, AMNH on entomological MAINE OSAC MIN UMEC CUIC MICH NY WIS EMC AMNH ISC CMNH CDFA INHS UDCC EMEC ILL CSUC MU CAS ILLS SEMC COLO MO UKIC KANU NCSU UCRC MEM Herbaria TEX Insect Collections TAMU BPBM Goals Plants Image and database 1.26M specimens from 20 families of vascular plants Unify these with 3.5M specimens from 3 data providers Mobilize total of 6.06M specimens Bugs Database 1.16M specimens from 92 families of Hemiptera Unify these with .38M specimens from 3 data providers Image selected specimens Parasitoids Database 45K specimens from 5 families of Hymenoptera Integrate trophic levels (7.65M records) in Discover Life Progress on Goals Start of Year 4 Botany: (currently at NY) 1,003 M images (79% of expected) data capture and georeferencing varies from skeletal to complete Insects + Parasitoids: 825K records completed (73.3% of expected) Happening Just Last Week Utilization of Collection Data Workshop UC-Riverside, June 17-18, 2014 data-mining and species distribution modeling use Tri-trophic Database as platform targeted to systematists and ecologists From Museum Specimen Database to Ecological Statement: Data Quality Inspection From Museum Specimen Database -
Hemiptera: Cercopoidea: Clastopteridae) Vinton Thompson1
Cicadina 12: 81-87 (2011) 81 Notes on the Biology of Clastoptera distincta Doering, the Dwarf Mistletoe Spittlebug (Hemiptera: Cercopoidea: Clastopteridae) Vinton Thompson1 Abstract: Nymphs of the spittlebug Clastoptera distincta Doering (Hemiptera: Cercopoidea: Clastopteridae) are xylem sap hyperparasites of the mistletoe Arceuthobium vaginatum subsp. cryptopodum, a parasite of Pinus ponderosa in the southwestern United States. C. distincta adults, which live directly on P. ponderosa, are polymorphic for three distinct color forms. Mistletoe feeding in the nymphal stage may be an adaptation to the regional monsoon climate, permitting the spittlebugs to take advantage of high mistletoe transpiration and xylem flow rates during the early summer dry season, when transpiration in the host trees is curtailed. Zusammenfassung: Larven der Schaumzikade Clastoptera distincta Doering (Hemiptera: Cercopoidea: Clastopteridae) sind Xylemsaft-Hyperparasiten an der Mistelart Arceuthobium vaginatum subsp. cryptopodum, einem Parasiten an Pinus ponderosa im Südwesten der Vereinigten Staaten. Die Adulten von C. distincta, die direct an P. ponderosa leben, sind polymorph bzgl. drei verschiedener Farbformen. Das Saugen an Misteln im Larvalstadium könnte eine Anpassung an das regionale Monsunklima sein, das es den Schaum- zikaden ermöglicht, von der hohen Transpirationrate und Xylemsaftflüssen während der Trockenphase im Frühsommer zu profitieren, wenn die Transpiration in der eigentlichen Nahrungspflanze eingeschränkt ist. Key words: spittlebug, Clastoptera, -
Insects and Related Arthropods Associated with of Agriculture
USDA United States Department Insects and Related Arthropods Associated with of Agriculture Forest Service Greenleaf Manzanita in Montane Chaparral Pacific Southwest Communities of Northeastern California Research Station General Technical Report Michael A. Valenti George T. Ferrell Alan A. Berryman PSW-GTR- 167 Publisher: Pacific Southwest Research Station Albany, California Forest Service Mailing address: U.S. Department of Agriculture PO Box 245, Berkeley CA 9470 1 -0245 Abstract Valenti, Michael A.; Ferrell, George T.; Berryman, Alan A. 1997. Insects and related arthropods associated with greenleaf manzanita in montane chaparral communities of northeastern California. Gen. Tech. Rep. PSW-GTR-167. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Dept. Agriculture; 26 p. September 1997 Specimens representing 19 orders and 169 arthropod families (mostly insects) were collected from greenleaf manzanita brushfields in northeastern California and identified to species whenever possible. More than500 taxa below the family level wereinventoried, and each listing includes relative frequency of encounter, life stages collected, and dominant role in the greenleaf manzanita community. Specific host relationships are included for some predators and parasitoids. Herbivores, predators, and parasitoids comprised the majority (80 percent) of identified insects and related taxa. Retrieval Terms: Arctostaphylos patula, arthropods, California, insects, manzanita The Authors Michael A. Valenti is Forest Health Specialist, Delaware Department of Agriculture, 2320 S. DuPont Hwy, Dover, DE 19901-5515. George T. Ferrell is a retired Research Entomologist, Pacific Southwest Research Station, 2400 Washington Ave., Redding, CA 96001. Alan A. Berryman is Professor of Entomology, Washington State University, Pullman, WA 99164-6382. All photographs were taken by Michael A. Valenti, except for Figure 2, which was taken by Amy H. -
Hemiptera, Prosorrhyncha) with Special Reference to the Pregenital Abdominal Structure1
© Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Justification for the Aradimorpha as an infraorder of the suborder Heteroptera (Hemiptera, Prosorrhyncha) with Special Reference to the Pregenital Abdominal Structure1 M.H. SWEET Abstract: Aradomorpha SWEET 1996 is replaced with Aradimorpha because of homonymy with Arado- morpha CHAMPION 1899, a genus of Reduviidae. The Aradimorpha differ from the Pentatomomorpha s.s. and the Leptopodomorpha in having a plesiomorphic connexivum of dorsal epipleurites and ventral hy- popleurites rather than having the connexivum turned over so that the hypopleurites are dorsalized and the epipleurites folded into the abdomen. In most Aradimorpha, in both males and females, sterna 3 to 7 are free with intersegmental conjunctiva; terga 1-2 and 3 to 6 are united, but all epipleurites are free. In the Pentatomomorpha at least abdominal sterna 2 to 4 in females and sterna 2 to 5 in males are uni- ted or fused without conjunctiva. In some aradids the hypopleurites are united or fused with the sterna, but hypopleurite 2 is usually free. Sternum 2 is sometimes united to fused with sternum 1 and the meta- sternum. The abdominal spiracles in the Aradimorpha are ventral on the hypopleurites, although some- times very lateral in position on the hypopleurites, with the exception of the Chinamyersiini in which spiracles 4, 5 and 6 are dorsal on the epipleurites in Chinamyersia, and 5 and 6 dorsal in Gnostocoris, whi- le in the Tretocorini (Tretocoris and Kumaressa) spiracle 2 seems dorsal but is actually very lateral on the hypopleurite. In the Termitaphididae, epipleurites and hypopleurites are distinct, forming mobile lateral abdominal lobes. -
Laboulbeniales on Semiaquatic Hemiptera. V. Triceromyces Richard K
Aliso: A Journal of Systematic and Evolutionary Botany Volume 11 | Issue 3 Article 2 1986 Laboulbeniales on semiaquatic Hemiptera. V. Triceromyces Richard K. Benjamin Rancho Santa Ana Botanic Garden Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Benjamin, Richard K. (1986) "Laboulbeniales on semiaquatic Hemiptera. V. Triceromyces," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 11: Iss. 3, Article 2. Available at: http://scholarship.claremont.edu/aliso/vol11/iss3/2 ALISO 11(3), 1986, pp. 245-278 LABOULBENIALES ON SEMIAQUATIC HEMIPTERA. V. TRICEROMYCES: WITH A DESCRIPTION OF MONOECIOUS-DIOECIOUS DIMORPHISM IN THE GENUS RICHARD K. BENJAMIN Rancho Santa Ana Botanic Garden Claremont, California 91711 ABSTRACf Six species of Triceromyces (Laboulbeniales), including the type, T. balazucii (on Hebridae), parasitic on semiaquatic Hemiptera, were studied at the light-microscopic level. Descriptions are provided for all of the taxa, and features of developmental morphology are described, compared, and illustrated with photographs and line drawings. Four species are described as new: T. hebri (on Hebridae), T. hydrometrae (on Hydrometridae), and T. bi/ormis and T. bullatus (on MesoveJiidae). The species growing on Hebridae and Hydrometridae are monoecious. The two species on Mesoveliidae develop monoecious and dioecious morphs, which occur together on the same host individual. This phenom enon is recognized and described for the first time in the Laboulbeniales. Two species, Autophagomyces poissonii and Dioicomyces mesoveliae, previously described from a species ofMesoveliidae, are shown to represent the monoecious and dioecious forms of a species of Triceromyces and are transferred to this genus as T. -
Cretaceous and Palaeogene Diversification of Planthoppers and Leafhoppers
Bulletin of Insectology 61 (1): 111-112, 2008 ISSN 1721-8861 Paradise Lost? – Cretaceous and Palaeogene diversification of planthoppers and leafhoppers Jacek SZWEDO Museum and Institute of Zoology, Polish Academy of Sciences, Warszawa, Poland Abstract History of the evolutionary changes of the Fulgoromorpha and Cicadomorpha (Hemiptera) in the Cretaceous and Palaeogene is shortly presented. Rapid differentiation and extinction of the groups is related to Mid-Cretaceous biotic events. Early Palaeogene is believed to be the time of dispersal of numerous groups, while Eocene greenhouse time as the period of differentiation and dis- persal of descendants of both lineages, including extinct groups. Oligocene cooling and further Miocene biotic changes as the times of origination of recent faunas are discussed in brief. Key words: Fulgoromorpha, Cicadomorpha, Cretaceous, Palaeogene, faunistic turnover. Introduction Mid-Cretaceous turnover The mid-Cretaceous is generally referred to as a Fulgoromorpha and Cicadomorpha are ancient lineages greenhouse period characterized by exceptionally warm of the Hemiptera, known since the Permian. The fossil climates. Mid-Cretaceous is regarded as a period of en- record and diversity of the ancient Fulgoromorpha have vironmental change and biotic crisis (Rasnitsyn, 1988). not been very high. Cicadomorpha appears more diver- Angiosperms were more frequent and abundant at lower sified since their beginnings. Roots of most of the recent latitudes in a dry (sub)tropical zone, at that time mainly groups of Fulgoromorpha and Cicadomorpha could be tropical Gondwanaland, though gymnospermous forests placed in the Jurassic, or even as far as in Triassic prevailed in wetter climates in the higher latitudes of (Shcherbakov and Popov, 2002; Szwedo et al., 2004). -
Great Lakes Entomologist the Grea T Lakes E N Omo L O G Is T Published by the Michigan Entomological Society Vol
The Great Lakes Entomologist THE GREA Published by the Michigan Entomological Society Vol. 45, Nos. 3 & 4 Fall/Winter 2012 Volume 45 Nos. 3 & 4 ISSN 0090-0222 T LAKES Table of Contents THE Scholar, Teacher, and Mentor: A Tribute to Dr. J. E. McPherson ..............................................i E N GREAT LAKES Dr. J. E. McPherson, Educator and Researcher Extraordinaire: Biographical Sketch and T List of Publications OMO Thomas J. Henry ..................................................................................................111 J.E. McPherson – A Career of Exemplary Service and Contributions to the Entomological ENTOMOLOGIST Society of America L O George G. Kennedy .............................................................................................124 G Mcphersonarcys, a New Genus for Pentatoma aequalis Say (Heteroptera: Pentatomidae) IS Donald B. Thomas ................................................................................................127 T The Stink Bugs (Hemiptera: Heteroptera: Pentatomidae) of Missouri Robert W. Sites, Kristin B. Simpson, and Diane L. Wood ............................................134 Tymbal Morphology and Co-occurrence of Spartina Sap-feeding Insects (Hemiptera: Auchenorrhyncha) Stephen W. Wilson ...............................................................................................164 Pentatomoidea (Hemiptera: Pentatomidae, Scutelleridae) Associated with the Dioecious Shrub Florida Rosemary, Ceratiola ericoides (Ericaceae) A. G. Wheeler, Jr. .................................................................................................183