Lacewings and Antlions
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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. -
The Green Lacewings of the Genus Chrysopa in Maryland ( Neuroptera: Chrysopidae)
The Green Lacewings of the Genus Chrysopa in Maryland ( Neuroptera: Chrysopidae) Ralph A. Bram and William E. Bickley Department of Entomology INTRODUCTION Tlw green lacewings which are members of the genus Chrysopa are extreme- ly lwndicia1 insects. The larvae are commonly called aphislions and are well known as predators of aphids and other injurious insects. They play an important part in the regulation of populations of pests under natural conditions, and in California they have been cultured in mass and released for the control of mealy- bugs ( Finney, 1948 and 1950) . The positive identification of members of the genus is desirable for the use of biological-control workers and entomologists in general. Descriptions of most of the Nearctic species of Chrysopidae have relied heavily on body pigmentation and to a lesser extent on wing shape, venational patterns and coloration. Specimens fade when preserved in alcohol or on pins, and natural variation in color patterns occurs in many species ( Smith 1922, Bickley 1952). It is partly for these reasons that some of the most common and relatively abundant representatives of the family are not easily recognized. The chrysopid fauna of North America was treated comprehensively by Banks ( 1903). Smith ( 1922) contributed valuable information about the biology of the green lacewings and about the morphology and taxonomy of the larvae. He also pro- vided k<'ys and other help for the identification of species from Kansas ( 1925, 1934) and Canada ( 1932). Froeschner ( 194 7) similarly dealt with Missouri species. Bickley and MacLeod ( 1956) presented a review of the family as known to occur in the N earctic region north of Mexico. -
Green Lacewings Family Chrysopidae
Beneficial Insects Class Insecta, Insects Order Neuroptera, Lacewings, mantids and others Neuroptera means “nerve wings” and refers to the hundreds of veins in their wings. The order Neuroptera is comprised of several small families. Larvae and adults are usually predaceous. Some families are uncommon while others are present more in the south and west. All neuropterans have chewing mouthparts. Green lacewings Family Chrysopidae Description and life history: Adults are green, 15–20 mm long, and slender. They have large, clear membranous wings with green veins and margins, which they hold over their body like a roof. Most have long hair-like antennae and golden eyes. Oval, white eggs are laid singly on a stalk approximately 8 mm long. Larvae are small, gray, and slender, and have large sickle-shaped mouthparts with which to puncture prey. When they reach approximately 10 mm, they spin a silken cocoon and pupate on the underside of a leaf. There are one to ten generations per year. Prey species: Green lacewing adults require high-energy foods such as honeydew and pollen. Larvae prey on aphids and other small, soft-bodied insects, and are nicknamed “aphid-lions.” Some adults are also preda- Green lacewing cocoons containing pupa. (357) ceous. Eggs, larvae, and adults are commercially avail- Photo: John Davidson able and may be purchased from insectaries. These common insects feed in fields, orchards, and gardens. They are commercially available. Chrysoperla carnea, green lacewing adult. (356) Photo: David Laughlin Green lacewing eggs on stalks. (359) Photo: John Davidson Green lacewing larva. (358) Photo: John Davidson IPM of Midwest Landscapes 278. -
Efficiency of Antlion Trap Construction
3510 The Journal of Experimental Biology 209, 3510-3515 Published by The Company of Biologists 2006 doi:10.1242/jeb.02401 Efficiency of antlion trap construction Arnold Fertin* and Jérôme Casas Université de Tours, IRBI UMR CNRS 6035, Parc Grandmont, 37200 Tours, France *Author for correspondence (e-mail: [email protected]) Accepted 21 June 2006 Summary Assessing the architectural optimality of animal physical constant of sand that defines the steepest possible constructions is in most cases extremely difficult, but is slope. Antlions produce efficient traps, with slopes steep feasible for antlion larvae, which dig simple pits in sand to enough to guide preys to their mouths without any attack, catch ants. Slope angle, conicity and the distance between and shallow enough to avoid the likelihood of avalanches the head and the trap bottom, known as off-centring, were typical of crater angles. The reasons for the paucity of measured using a precise scanning device. Complete attack simplest and most efficient traps such as theses in the sequences in the same pits were then quantified, with animal kingdom are discussed. predation cost related to the number of behavioural items before capture. Off-centring leads to a loss of architectural efficiency that is compensated by complex attack Supplementary material available online at behaviour. Off-centring happened in half of the cases and http://jeb.biologists.org/cgi/content/full/209/18/3510/DC1 corresponded to post-construction movements. In the absence of off-centring, the trap is perfectly conical and Key words: animal construction, antlion pit, sit-and-wait predation, the angle is significantly smaller than the crater angle, a physics of sand, psammophily. -
Pidae, Osmylin
NATHAN BANKS. 201 SYNOPSES AND DESCRIPTIONS OF EXOTIC NEUROPTERA. Included below, with the descriptions of various new genera and species, are synopses of the genera of Panos- pidae, Osmylinae, Hemerobiinae, Mantispidae, South Ameri- can Myrmeleonidae and a new classification of the Perlidae ; most of the synoptic work is a result of a study of several European collections. The types of all the new species described in this paper are in the author's collection. PERLIDAE. Twice I have published classifications of the American Perlidae. After seeing several genera (hitherto unknown to me) in European museums I have prepared a new ar- rangement, which, however, differs little from the others as far as American species are concerned, but places in the same scheme the various exotic genera. For the principal character I would use the shape of the anterior part of the head. 1. Clypeus practically invisible, or only projecting from beneath the raised margin of the front of the head ; tarsi with the last joint very much longer than the first and second together, the first joint barely, if any longer, than the width of the tibia at tip; coxae I widely separate; setae present; no series of cross-veins in the cubito-anal space..... PERLINAE. Clypeus visible in continuation of the general surface of the head, and separated by a suture from the head ; tarsi with the last joint but little or not longer than the first and second together, the first joint longer than the width of the tibiae at tip, last joint of palpi as large as others ....................... -
UFRJ a Paleoentomofauna Brasileira
Anuário do Instituto de Geociências - UFRJ www.anuario.igeo.ufrj.br A Paleoentomofauna Brasileira: Cenário Atual The Brazilian Fossil Insects: Current Scenario Dionizio Angelo de Moura-Júnior; Sandro Marcelo Scheler & Antonio Carlos Sequeira Fernandes Universidade Federal do Rio de Janeiro, Programa de Pós-Graduação em Geociências: Patrimônio Geopaleontológico, Museu Nacional, Quinta da Boa Vista s/nº, São Cristóvão, 20940-040. Rio de Janeiro, RJ, Brasil. E-mails: [email protected]; [email protected]; [email protected] Recebido em: 24/01/2018 Aprovado em: 08/03/2018 DOI: http://dx.doi.org/10.11137/2018_1_142_166 Resumo O presente trabalho fornece um panorama geral sobre o conhecimento da paleoentomologia brasileira até o presente, abordando insetos do Paleozoico, Mesozoico e Cenozoico, incluindo a atualização das espécies publicadas até o momento após a última grande revisão bibliográica, mencionando ainda as unidades geológicas em que ocorrem e os trabalhos relacionados. Palavras-chave: Paleoentomologia; insetos fósseis; Brasil Abstract This paper provides an overview of the Brazilian palaeoentomology, about insects Paleozoic, Mesozoic and Cenozoic, including the review of the published species at the present. It was analiyzed the geological units of occurrence and the related literature. Keywords: Palaeoentomology; fossil insects; Brazil Anuário do Instituto de Geociências - UFRJ 142 ISSN 0101-9759 e-ISSN 1982-3908 - Vol. 41 - 1 / 2018 p. 142-166 A Paleoentomofauna Brasileira: Cenário Atual Dionizio Angelo de Moura-Júnior; Sandro Marcelo Schefler & Antonio Carlos Sequeira Fernandes 1 Introdução Devoniano Superior (Engel & Grimaldi, 2004). Os insetos são um dos primeiros organismos Algumas ordens como Blattodea, Hemiptera, Odonata, Ephemeroptera e Psocopera surgiram a colonizar os ambientes terrestres e aquáticos no Carbonífero com ocorrências até o recente, continentais (Engel & Grimaldi, 2004). -
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. -
Jumping Mechanisms in Lacewings (Neuroptera, Chrysopidae And
© 2014. Published by The Company of Biologists Ltd | The Journal of Experimental Biology (2014) 217, 4252-4261 doi:10.1242/jeb.110841 RESEARCH ARTICLE Jumping mechanisms in lacewings (Neuroptera, Chrysopidae and Hemerobiidae) Malcolm Burrows1,* and Marina Dorosenko1 ABSTRACT increases the complexity of muscle control but has the advantage of Lacewings launch themselves into the air by simultaneous propulsive increasing the muscle mass that can be devoted to jumping while movements of the middle and hind legs as revealed in video images avoiding the specialisation in shape and size of the legs. In snow captured at a rate of 1000 s−1. These movements were powered fleas it also allows four energy stores – one for each leg – to be used largely by thoracic trochanteral depressor muscles but did not start in its catapult jumping action (Burrows, 2011). Furthermore, by from a particular preset position of these legs. Ridges on the lateral distributing ground reaction forces over a larger surface area, take- sides of the meso- and metathorax fluoresced bright blue when off becomes possible from more compliant surfaces. For the fly illuminated with ultraviolet light, suggesting the presence of the elastic Hydrophorus alboflorens this even enables jumping from the surface protein resilin. The middle and hind legs were longer than the front of water by ensuring that the legs do not penetrate the surface legs but their femora and tibiae were narrow tubes of similar (Burrows, 2013a). diameter. Jumps were of two types. First, those in which the body In all jumping movements, the same demands exist for high take- was oriented almost parallel to the ground (−7±8 deg in green off velocities and short acceleration times, particularly when escape lacewings, 13.7±7 deg in brown lacewings) at take-off and remained is the required outcome. -
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) from the Upper Cenomanian Nizhnyaya Agapa Amber, Northern Siberia
Cretaceous Research 93 (2019) 107e113 Contents lists available at ScienceDirect Cretaceous Research journal homepage: www.elsevier.com/locate/CretRes Short communication New Coniopterygidae (Neuroptera) from the upper Cenomanian Nizhnyaya Agapa amber, northern Siberia * Vladimir N. Makarkin a, Evgeny E. Perkovsky b, a Federal Scientific Center of the East Asia Terrestrial Biodiversity, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok, 690022, Russia b Schmalhausen Institute of Zoology, National Academy of Sciences of Ukraine, ul. Bogdana Khmel'nitskogo 15, Kiev, 01601, Ukraine article info abstract Article history: Libanoconis siberica sp. nov. and two specimens of uncertain affinities (Neuroptera: Coniopterygidae) are Received 28 April 2018 described from the Upper Cretaceous (upper Cenomanian) Nizhnyaya Agapa amber, northern Siberia. Received in revised form The new species is distinguished from L. fadiacra (Whalley, 1980) by the position of the crossvein 3r-m 9 August 2018 being at a right angle to both RP1 and the anterior trace of M in both wings. The validity of the genus Accepted in revised form 11 September Libanoconis is discussed. It easily differs from all other Aleuropteryginae by a set of plesiomorphic 2018 Available online 15 September 2018 character states. The climatic conditions at high latitudes in the late Cenomanian were favourable enough for this tropical genus, hitherto known from the Gondwanan Lebanese amber. Therefore, the Keywords: record of a species of Libanoconis in northern Siberia is highly likely. © Neuroptera 2018 Elsevier Ltd. All rights reserved. Coniopterygidae Aleuropteryginae Cenomanian Nizhnyaya Agapa amber 1. Introduction 2. Material and methods The small-sized neuropteran family Coniopterygidae comprises This study is based on three specimens originally embedded in ca. -
From Chewing to Sucking Via Phylogeny—From Sucking to Chewing Via Ontogeny: Mouthparts of Neuroptera
Chapter 11 From Chewing to Sucking via Phylogeny—From Sucking to Chewing via Ontogeny: Mouthparts of Neuroptera Dominique Zimmermann, Susanne Randolf, and Ulrike Aspöck Abstract The Neuroptera are highly heterogeneous endopterygote insects. While their relatives Megaloptera and Raphidioptera have biting mouthparts also in their larval stage, the larvae of Neuroptera are characterized by conspicuous sucking jaws that are used to imbibe fluids, mostly the haemolymph of prey. They comprise a mandibular and a maxillary part and can be curved or straight, long or short. In the pupal stages, a transformation from the larval sucking to adult biting and chewing mouthparts takes place. The development during metamorphosis indicates that the larval maxillary stylet contains the Anlagen of different parts of the adult maxilla and that the larval mandibular stylet is a lateral outgrowth of the mandible. The mouth- parts of extant adult Neuroptera are of the biting and chewing functional type, whereas from the Mesozoic era forms with siphonate mouthparts are also known. Various food sources are used in larvae and in particular in adult Neuroptera. Morphological adaptations of the mouthparts of adult Neuroptera to the feeding on honeydew, pollen and arthropods are described in several examples. New hypoth- eses on the diet of adult Nevrorthidae and Dilaridae are presented. 11.1 Introduction The order Neuroptera, comprising about 5820 species (Oswald and Machado 2018), constitutes together with its sister group, the order Megaloptera (about 370 species), and their joint sister group Raphidioptera (about 250 species) the superorder Neuropterida. Neuroptera, formerly called Planipennia, are distributed worldwide and comprise 16 families of extremely heterogeneous insects. -
Universidade Federal Do Ceará Centro De Ciências Departamento De Geologia Programa De Pós-Graduação Em Geologia Luís Carlo
1 UNIVERSIDADE FEDERAL DO CEARÁ CENTRO DE CIÊNCIAS DEPARTAMENTO DE GEOLOGIA PROGRAMA DE PÓS-GRADUAÇÃO EM GEOLOGIA LUÍS CARLOS BASTOS FREITAS DESCRIÇÃO DE NOVOS TAXONS DE INSETOS FÓSSEIS DOS MEMBROS CRATO E ROMUALDO DA FORMAÇÃO SANTANA E COMENTÁRIOS SOBRE A GEODIVERSIDADE DO GEOPARK ARARIPE, BACIA SEDIMENTAR DO ARARIPE, NORDESTE DO BRASIL FORTALEZA 2019 2 LUÍS CARLOS BASTOS FREITAS DESCRIÇÃO DE NOVOS TAXONS DE INSETOS FÓSSEIS DOS MEMBROS CRATO E ROMUALDO DA FORMAÇÃO SANTANA E COMENTÁRIOS SOBRE A GEODIVERSIDADE DO GEOPARK ARARIPE, BACIA SEDIMENTAR DO ARARIPE, NORDESTE DO BRASIL Tese apresentada ao Programa de Pós- Graduação em Geologia da Universidade Federal do Ceará, como requisito parcial à obtenção do título de doutor em Geologia. Área de concentração: Geologia Sedimentar e Paleontologia. Orientador: Prof. Dr. Geraldo Jorge Barbosa de Moura. Coorientador: Prof. Dr. César Ulisses Vieira Veríssimo. FORTALEZA 2019 3 4 LUÍS CARLOS BASTOS FREITAS DESCRIÇÃO DE NOVOS TAXONS DE INSETOS FÓSSEIS DOS MEMBROS CRATO E ROMUALDO DA FORMAÇÃO SANTANA E COMENTÁRIOS SOBRE A GEODIVERSIDADE DO GEOPARK ARARIPE, BACIA SEDIMENTAR DO ARARIPE, NORDESTE DO BRASIL Tese apresentada ao Programa de Pós- Graduação em Geologia da Universidade Federal do Ceará, como requisito parcial à obtenção do título de doutor em Geologia. Área de concentração: Geologia Sedimentar e Paleontologia. Aprovada em: 18/01/2019. BANCA EXAMINADORA ________________________________________ Prof. Dr. Geraldo Jorge Barbosa de Moura (Orientador) Universidade Federal Rural de Pernambuco (UFRPE) _________________________________________ Prof. Dr. Marcio Mendes (Interno) Universidade Federal do Ceará (UFC) _________________________________________ Prof. Dr. Marcos Antônio Leite do Nascimento (Externo) Universidade Federal do Rio Grande do Norte (UFRN) _________________________________________ Prof. Dr Kleberson de Oliveira Porpino (Externo) Universidade do Estado do Rio Grande do Norte (UERN) ________________________________________ Dra Pâmela Moura (Externo) Universidade Federal do Ceará (UFC) 5 A Deus.