Neuroptera, Chrysopidae): I
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Neuroptera (Lacewings, Doodlebugs, Antlions)
Return to insect order home Page 1 of 2 Visit us on the Web: www.gardeninghelp.org Insect Order ID: Neuroptera (Lacewings, Doodlebugs, Antlions) Life Cycle–Complete metamorphosis. Adults lay eggs. Larvae eat, grow and molt. This stage is repeated a varying number of times, depending on species, until hormonal changes cause the larvae to pupate. Inside the pupal case, they change in form and color and develop wings. The adults look completely different from the larvae. Adults–Lacewings have clear membranous wings with numerous cells, hence the name Neuroptera "nerve wing." The forewing and hindwing are about the same size. The eyes are large in relationship to the head, like glittering beads. (Click images to enlarge or orange text for more information.) Colors vary Numerous cells in wings Bright beadlike eyes from brown to green Eggs–The eggs of many species are laid at the end of a hairlike stalk. (Click images to enlarge or orange text for more information.) Lacewing eggs laid on a stalk Lacewing egg Return to insect order home Page 2 of 2 Larvae–All are campodeiform, spiny and soft-bodied with large hollow mandibles used to skewer victims and suck them dry. Some species place the dried remains of their victims on the spines on their backs, giving them the appearance of walking trash heaps. (Click images to enlarge or orange text for more information.) Campodeiform Large, hollow mandibles Hidden beneath the spiny, soft-bodied Campodeiform remains of its victim Pupae–All have a pupal stage, usually a silken cocoon, during which the adult, winged form develops. -
Fish, Various Invertebrates
Zambezi Basin Wetlands Volume II : Chapters 7 - 11 - Contents i Back to links page CONTENTS VOLUME II Technical Reviews Page CHAPTER 7 : FRESHWATER FISHES .............................. 393 7.1 Introduction .................................................................... 393 7.2 The origin and zoogeography of Zambezian fishes ....... 393 7.3 Ichthyological regions of the Zambezi .......................... 404 7.4 Threats to biodiversity ................................................... 416 7.5 Wetlands of special interest .......................................... 432 7.6 Conservation and future directions ............................... 440 7.7 References ..................................................................... 443 TABLE 7.2: The fishes of the Zambezi River system .............. 449 APPENDIX 7.1 : Zambezi Delta Survey .................................. 461 CHAPTER 8 : FRESHWATER MOLLUSCS ................... 487 8.1 Introduction ................................................................. 487 8.2 Literature review ......................................................... 488 8.3 The Zambezi River basin ............................................ 489 8.4 The Molluscan fauna .................................................. 491 8.5 Biogeography ............................................................... 508 8.6 Biomphalaria, Bulinis and Schistosomiasis ................ 515 8.7 Conservation ................................................................ 516 8.8 Further investigations ................................................. -
The Chrysopidae of Canada (Neuroptera): Recent Acquisitions Chiefly in British Columbia and Yukon
.I. ENTOMOL. soc. BRIT. COLUMBIA 97. DECEMBER 2000 39 The Chrysopidae of Canada (Neuroptera): recent acquisitions chiefly in British Columbia and Yukon J. A. GARLAND 1011 CARLING AVENUE, OTTAWA, ONTARIO, CANADA KI Y 4E7 ABSTRACT Chryso pidae collected sin ce 1980 chiefly in British Co lumbi a and Yuk on, Canada, and some late additi ons co ll ected before \980, are reported. :Vinela gravida (Banks) is reported for th e first time in th e last 90 years. This is th e first supplement to th e inventory of Chryso pid ae in Can ada. Key words: Ne uroptera, Chryso pidae, Canada INTRODUCTION The chrysopid faun a of Canada, as presentl y und erstood (Garland 1984, 1985), has been full y in ve ntori ed up to 1980 (Garl and 1982). Since then , newl y co ll ected specimens in British Columbia and th e Yukon, and some older-dated specimens not previously seen, have become availabl e. The purpose of publishing th ese spec imen label data is to suppl ement th e already extensive in ve ntory oflabel data on th e Ca nadi an chrysopid fauna, thereby ex tending it to the year 2000. Materi als an d meth ods appropri ate to thi s study have been doc um ented elsewhere (Garl and 2000). All specimens reported here are depos it ed in the Spence r Entomologica l Museum, Department of Zoo logy, University of Briti sh Co lumbi a. Ac ronyms used below: BC , British Co lumbia; SK, Sas katch ewan; and YK , Yukon Territory. -
The First Green Lacewings from the Late Eocene Baltic Amber
The first green lacewings from the late Eocene Baltic amber VLADIMIR N. MAKARKIN, SONJA WEDMANN, and THOMAS WEITERSCHAN Makarkin, V.N., Wedmann, S., and Weiterschan, T. 2018. The first green lacewings from the late Eocene Baltic amber. Acta Palaeontologica Polonica 63 (3): 527–537. Pseudosencera baltica gen. et sp. nov. of Chrysopinae (Chrysopidae, Neuroptera) is described from Baltic amber. Additionally, another species, Nothochrysa? sp. (Nothochrysinae), is left in the open nomenclature. Pseudosencera bal- tica gen. et sp. nov. represents the oldest confident record of Chrysopinae. The new genus lacks the apparent forewing intramedian cell, and possesses three character states not found in other Chrysopinae: the simple AA1, the short basal crossvein between M and Cu, and 5‒6 rings of setae on the antennal flagellomeres. This genus is probably a special- ised form in a basal branch of Chrysopinae, that could not be attributed to any of the known tribes. The specimen of Nothochrysa? sp. consists only of fragments of the forewings. The late Eocene Baltic amber represents the oldest horizon where Chrysopinae and Nothochrysinae are found to coexist. It is highly likely that Chrysopidae were extremely rare in these forests. Key words: Neuroptera, Chrysopinae, Nothochrysinae, Cenozoic, Baltic amber. Vladimir N. Makarkin [[email protected]], Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok 690022, Russia. Sonja Wedmann [[email protected]], Senckenberg Forschungsstation Grube Messel, Markstrasse 35, D-64409 Messel, Germany. Thomas Weiterschan [[email protected]], Forsteler Strasse 1, 64739 Höchst Odw., Germany. Received 16 May 2018, accepted 5 July 2018, available online 23 July 2018. -
Prey Recognition in Larvae of the Antlion Euroleon Nostras (Neuroptera, Myrrneleontidae)
Acta Zool. Fennica 209: 157-161 ISBN 95 1-9481-54-0 ISSN 0001-7299 Helsinki 6 May 1998 O Finnish Zoological and Botanical Publishing Board 1998 Prey recognition in larvae of the antlion Euroleon nostras (Neuroptera, Myrrneleontidae) Bojana Mencinger Mencinger, B., Department of Biology, University ofMaribor, Koro&a 160, SLO-2000 Maribor, Slovenia Received 14 July 1997 The behavioural responses of the antlion larva Euroleon nostras to substrate vibrational stimuli from three species of prey (Tenebrio molitor, Trachelipus sp., Pyrrhocoris apterus) were studied. The larva reacted to the prey with several behavioural patterns. The larva recognized its prey at a distance of 3 to 15 cm from the rim of the pit without seeing it, and was able to determine the target angle. The greatest distance of sand tossing was 6 cm. Responsiveness to the substrate vibration caused by the bug Pyrrhocoris apterus was very low. 1. Introduction efficient motion for antlion is to toss sand over its back (Lucas 1989). When the angle between the The larvae of the European antlion Euroleon head in resting position and the head during sand nostras are predators as well as the adults. In loose tossing is 4S0, the section of the sand tossing is substrate, such as dry sand, they construct coni- 30" (Koch 1981, Koch & Bongers 1981). cal pits. At the bottom of the pit they wait for the Sensitivity to vibration in sand has been stud- prey, which slides into the trap. Only the head ied in a few arthropods, e.g. in the nocturnal scor- and sometimes the pronotum of the larva are vis- pion Paruroctonus mesaensis and the fiddler crab ible; the other parts of the body are covered with Uca pugilator. -
Neuroptera: Chrysopidae)
Zootaxa 3351: 1–14 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) A new genus of Neotropical Chrysopini (Neuroptera: Chrysopidae) FRANCISCO SOSA1 & SERGIO DE FREITAS2 1 Universidad Centroccidental “Lisandro Alvarado”, Museo Entomológico “Dr. José Manuel Osorio” (UCOB), Barquisimeto, Lara, . E-mail: [email protected] 2 Universidade Estadual Paulista, Jaboticabal, São Paulo, Brazil (deceased) Abstract Titanochrysa Sosa & Freitas is a new genus of Neotropical Chrysopini (Chrysopidae: Chrysopinae) recorded from Costa Rica, Venezuela and Brazil. Titanochrysa gen. nov. shares several external and genitalic characters with Ceraeochrysa Adams, 1982; Chrysopodes Navás, 1913; Cryptochrysa Freitas & Penny, 2000; Parachrysopiella Brooks & Barnard, 1990 and Ungla Navás 1914. It may be distinguished from those genera by its very long sternite 8+9, sternites 2–8 usually with microtholi, male geni- talia with the dorsal surface of the arcessus striated, gonosaccus well-developed, bearing elongate gonosetae and microsetae, and a spoon-like gonapsis. Herein, Titanochrysa circumfusa (Burmeister, 1939) [= Chrysopodes circumfusa (Burmeister)] comb. nov. and Titanochrysa pseudovaricosa (Penny) [= Ceraeochrysa pseudovaricosa Penny, 1998] comb. nov. were identi- fied; Titanochrysa ferreirai Sosa & Freitas sp. nov. and Titanochrysa trespuntensis Sosa & Freitas sp. nov. were described. The external morphology, and male and female genitalia of all these species -
A Checklist of the Neuropterid Insects of British Columbia (Insecta: M Egaloptera, Neuroptera and Raphidioptera) with a Summary of Their Geographic Distribution
J. ENTOMOL. SOC. BRIT. COLUMBIA 106, DECEMBER 2009 17 A checklist of the Neuropterid insects of British Columbia (Insecta: M egaloptera, Neuroptera and Raphidioptera) with a summary of their geographic distribution GEOFFREY G.E. SCUDDER1 and ROBERT A. CANNINGS2 ABSTRACT The Neuropterid orders in British Columbia consist of the Megaloptera, Neuroptera and Raphidioptera. Twelve families containing 89 species are represented. The distribution of these species is documented with reference to the 9 terrestrial ecoprovinces in British Columbia. Collection localities are given for species represented by 5 or fewer sites. Four species, 2 of Coniopterygidae and 2 of Hemerobiidae, are considered alien intro- ductions. INTRODUCTION The first list of British Columbia (BC) order, the Neuroptera. Most of the more neuropterid insects was published by recent research on these 3 taxa in BC, Spencer (1942) at a time when the 3 orders which include both aquatic and terrestrial in this group of insects that occur in the species, was summarized by Cannings and province (Megaloptera, Neuroptera and Scudder (2001) and Scudder et al. (2001). Raphidioptera) were considered as a single M ATERIALS AND M ETHODS The list of species here considered as recorded. An ecoprovince is an area with occurring in BC follows the classification consistent climatic or oceanographic, to- of Oswald and Penny (1991) and Penny et pographic and geological history al. (1997), with some nomenclature (Meidinger and Pojar 1991, Demarchi changes published since. In the recent lit- 1996). There are 10 ecoprovinces in BC; erature, Garland and Kevan (2007) have their size and broad internal uniformity discussed the Chrysopidae, and Cannings make them ideal units for the general dis- and Cannings (2006) the Mantispidae. -
Pocket Guide to the Beneficial Insects of New Mexico
Pocket Guide to the Beneficial Insects of New Mexico Tessa R. Grasswitz, New Mexico State University Agricultural Science Center, Los Lunas, NM David R. Dreesen, Natural Resources Conservation Service Plant Materials Center, Los Lunas, NM 1 Contents Introduction ...........................................................3 Attracting and retaining beneficial insects .................4 Suggested insectary plants for New Mexico ...............5 Other ways to conserve beneficial insects .................7 Common beneficial insects of New Mexico 1. Beetles (Order: Coleoptera) .............................9 (i) Ladybeetles/Ladybird beetles (Coccinellidae) .......9 (ii) Ground beetles (Carabidae)......................11 (iii) Rove beetles (Staphylinidae) .....................12 (iv) Soft-winged flower beetles (Melyridae) .......13 2. True bugs (Order: Hemiptera) ........................14 (i) Big-eyed bugs (Georcoris species) ..............14 (ii) Minute pirate bugs (Anthocoridae) .............15 (iii) Damsel or nabid bugs (Nabidae) ..............16 (iv) Spined soldier bug (Podisus maculiventris) ...... 17 (v) Assassin bugs (Reduviidae) ........................18 3. Lacewings (Order: Neuroptera) .....................19 4. Beneficial flies (Order: Diptera) ......................20 (i) Hoverflies (Syrphidae) ................................20 (ii) Tachinid flies (Tachinidae) ......................21 5. Wasps (Order: Hymenoptera) ........................22 (i) Parasitic wasps (various families) ................22 (ii) Predatory wasps (various families) -
Preference of Antlion and Wormlion Larvae (Neuroptera: Myrmeleontidae; Diptera: Vermileonidae) for Substrates According to Substrate Particle Sizes
Eur. J. Entomol. 112(3): 000–000, 2015 doi: 10.14411/eje.2015.052 ISSN 1210-5759 (print), 1802-8829 (online) Preference of antlion and wormlion larvae (Neuroptera: Myrmeleontidae; Diptera: Vermileonidae) for substrates according to substrate particle sizes Dušan DEVETAK 1 and AMY E. ARNETT 2 1 Department of Biology, Faculty of Natural Sciences and Mathematics, University of Maribor, Koroška cesta 160, SI-2000 Maribor, Slovenia; e-mail: [email protected] 2 Center for Biodiversity, Unity College, 90 Quaker Hill Road, Unity, ME 04915, U.S.A.; e-mail: [email protected] Key words. Neuroptera, Myrmeleontidae, Diptera, Vermileonidae, antlions, wormlions, substrate particle size, substrate selection, pit-builder, non-pit-builder, habitat selection Abstract. Sand-dwelling wormlion and antlion larvae are predators with a highly specialized hunting strategy, which either construct efficient pitfall traps or bury themselves in the sand ambushing prey on the surface. We studied the role substrate particle size plays in these specialized predators. Working with thirteen species of antlions and one species of wormlion, we quantified the substrate particle size in which the species were naturally found. Based on these particle sizes, four substrate types were established: fine substrates, fine to medium substrates, medium substrates, and coarse substrates. Larvae preferring the fine substrates were the wormlion Lampromyia and the antlion Myrmeleon hyalinus originating from desert habitats. Larvae preferring fine to medium and medium substrates belonged to antlion genera Cueta, Euroleon, Myrmeleon, Nophis and Synclisis and antlion larvae preferring coarse substrates were in the genera Distoleon and Neuroleon. In addition to analyzing naturally-occurring substrate, we hypothesized that these insect larvae will prefer the substrate type that they are found in. -
INSECTS of MICRONESIA Neuroptera: Hemerobiidae*
INSECTS OF MICRONESIA Neuroptera: Hemerobiidae* By F. M. CARPENTER HARVARD UNIVERSITY INTRODUCTION This account is based mainly on about 150 specimens of Hemerobiidae from Micronesia. All of this material was placed at my disposal through the courtesy of Dr. J. L. Gressitt, to whom I am indebted for the opportunity of making this study. The United States Office of Naval Research, the Pacific Science Board (National Research Council), the National Science Foundation, and Bernice P. Bishop Museum have made this survey and publication of the results pos sible. Field research was aided by a contract between the Office of Naval Re search, Department of the Navy, and the National Academy of Sciences, NR 160-175. In the course of this study I have made much use of specimens in the Mu seum of Comparative Zoology and I have been helped to an inestimable extent by my examination of a type of Micromus navigatorum Brauer, sent to me by Dr. Beier of the Naturhistorisches Museum in Vienna. Specimens are deposited at the following institutions: Bernice P. Bishop Museum (BISHOP), United States National Museum (US), and Museum of Comparative Zoology, Harvard University (MCZ). Only three species are represented in this Micronesian collection, two in Annandalia and the third in Micromus. The third species, M. navigatorum, has now acquired a very wide distribution, in part, at least, through the agency of man. The two species of Annandalia are, so far as now known, endemic to Micronesia. Annandalia and Micromus are only distantly' related within the family Hemerobiidae and they can readily be distinguished: Annandalia has a broad costal area basally, with a well developed recurrent vein; Micromus has a narrow costal area basally and lacks entirely the recurrent vein. -
Of the World
OCCASIONAL PAPERS OF THE CALIFORNIA ACADEMY OF SCIENCES No. 147, 94 pages. December 2, 1991 GENUS-GROUP NAMES OF THE NEUROPTERA, MEGALOPTERA AND RAPHIDIOPTERA OF THE WORLD By John D. Oswald Department of Entomology, Cornell University, Ithaca, New York 14853-0999 and Norman D. Penny Department of Entomology, California Academy of Sciences, San Francisco, California 94118-4599 Abstract: Alphabetical listings of the genus-group names of extant Megaluptcra, Raphidioptera, and = Neuroptera (s. str. Planipennia) are presented. Taxonomic and nomenclatural data for each name are given. Summaries of new genus-group synonyms, unreplaced junior homonyms, names without valid type species fixations, and names based on misidentified type species are given. Complete bibliographic references are given for all names and nomenclatural acts. Contents Introduction Inlroduciion (1) The last worldwide species-level catalog of Scope (2) the order str. = Nomenclature (2) Neuroptera (s. Planipennia), and Format Arrangement of Entries (2) Hermann Hagen's 1866 Hemerobidarum Syn- General Arrangement (2) opsis Synonymica, has long been obsolete, as Subgenera (2) are the most recent revisions Synonymy (2) comprehensive Character Formals (3) of the orders Megaloptera (i.e.. Van dcr Publication Dates (3) Weele 1910) and Raphidioptera (i.e., Navas Type Species (3) [1919e] 1918). In the 120+ years since 1866, Unavailable Names (3) the number of available Homonymy (4) nomenclaturally Family-Group Taxa (4) genus-group names in the order Neuroptera Selected Taxonomic References -
Electrophoretic Studies in the Genus Chrysopa (S
Progress in World's Neuropterology. Gepp J-, H. Aspöck & H. Hölzel ed., 265 pp~, 1984, Graz. Electrophoretic Studies in the Genus Chrysopa (s. 1.), Evolutionary and Phylogenetic Inferences By L. BULLINI (Rome), M. M. PRINCIPI (Bologna) and R. CIANCIO (Rome) The taxonomy at the genus level of the subfamily Chrysopinae, and particularly of the old genus Chrysopa LEACH, represents till now an open problem. Different attempts of classification were made by several authors. TJEDER (1966,1972) splitted the genus Chrysopa (s. 1.) in various genera and subdivided the genus Chrysopa (s. str.) in a number of subgenera, on the basis of differences in male genital urites and external genital organs. This subdivision appears supported by studies on abdomen morphology of imagoes and on larval morphology, ethology and development, carried out by PRINCIPI (1977). HÖLZEL (1970) considered in the genus Chrysopa (s. str.) only the species with distinct 8° and 9° urosternites, including in other genera the species presenting them fused. The genus Anisochrysa sensu HÖLZEL (1970) comprehended two remarkably differentiated groups of species: the subgenera Chrysoperla and Anisochrysa, differing for genitalia and lar- val morphology, development and ethology, as pointed out by PRINCIPI (1956, 1977) and SÉMÉRIA (1977). The latter author proposed on such bases to consider Chrysoperla as a distinct genus. Finally, Chrysopa (s. str.), Chrysoperla and Anisochrysa were considered as distinct genera by ASPÖCK et al. (1980) in their recent revision on European Neuroptera. The problem of the phylogenetic relationships among the species of the genus Chrysopa (sensu latu) was approached by us with multilocus electrophoretic techniques. Their use in taxonomy and the evidence they provide for phylogenetic interpretation were pointed out in a number of recent papers (see for instance AVISE, 1975; BULLINI and SBORDONI, 1980).