Paleontological Contributions
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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. -
Burmese Amber Taxa
Burmese (Myanmar) amber taxa, on-line supplement v.2021.1 Andrew J. Ross 21/06/2021 Principal Curator of Palaeobiology Department of Natural Sciences National Museums Scotland Chambers St. Edinburgh EH1 1JF E-mail: [email protected] Dr Andrew Ross | National Museums Scotland (nms.ac.uk) This taxonomic list is a supplement to Ross (2021) and follows the same format. It includes taxa described or recorded from the beginning of January 2021 up to the end of May 2021, plus 3 species that were named in 2020 which were missed. Please note that only higher taxa that include new taxa or changed/corrected records are listed below. The list is until the end of May, however some papers published in June are listed in the ‘in press’ section at the end, but taxa from these are not yet included in the checklist. As per the previous on-line checklists, in the bibliography page numbers have been added (in blue) to those papers that were published on-line previously without page numbers. New additions or changes to the previously published list and supplements are marked in blue, corrections are marked in red. In Ross (2021) new species of spider from Wunderlich & Müller (2020) were listed as being authored by both authors because there was no indication next to the new name to indicate otherwise, however in the introduction it was indicated that the author of the new taxa was Wunderlich only. Where there have been subsequent taxonomic changes to any of these species the authorship has been corrected below. -
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. -
Insecta: Psocodea: 'Psocoptera'
Molecular systematics of the suborder Trogiomorpha (Insecta: Title Psocodea: 'Psocoptera') Author(s) Yoshizawa, Kazunori; Lienhard, Charles; Johnson, Kevin P. Citation Zoological Journal of the Linnean Society, 146(2): 287-299 Issue Date 2006-02 DOI Doc URL http://hdl.handle.net/2115/43134 The definitive version is available at www.blackwell- Right synergy.com Type article (author version) Additional Information File Information 2006zjls-1.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Blackwell Science, LtdOxford, UKZOJZoological Journal of the Linnean Society0024-4082The Lin- nean Society of London, 2006? 2006 146? •••• zoj_207.fm Original Article MOLECULAR SYSTEMATICS OF THE SUBORDER TROGIOMORPHA K. YOSHIZAWA ET AL. Zoological Journal of the Linnean Society, 2006, 146, ••–••. With 3 figures Molecular systematics of the suborder Trogiomorpha (Insecta: Psocodea: ‘Psocoptera’) KAZUNORI YOSHIZAWA1*, CHARLES LIENHARD2 and KEVIN P. JOHNSON3 1Systematic Entomology, Graduate School of Agriculture, Hokkaido University, Sapporo 060-8589, Japan 2Natural History Museum, c.p. 6434, CH-1211, Geneva 6, Switzerland 3Illinois Natural History Survey, 607 East Peabody Drive, Champaign, IL 61820, USA Received March 2005; accepted for publication July 2005 Phylogenetic relationships among extant families in the suborder Trogiomorpha (Insecta: Psocodea: ‘Psocoptera’) 1 were inferred from partial sequences of the nuclear 18S rRNA and Histone 3 and mitochondrial 16S rRNA genes. Analyses of these data produced trees that largely supported the traditional classification; however, monophyly of the infraorder Psocathropetae (= Psyllipsocidae + Prionoglarididae) was not recovered. Instead, the family Psyllipso- cidae was recovered as the sister taxon to the infraorder Atropetae (= Lepidopsocidae + Trogiidae + Psoquillidae), and the Prionoglarididae was recovered as sister to all other families in the suborder. -
Novitates Paleoentomologicae No
Novitates Paleoentomologicae No. 13, pp. 1–22 30 December 2015 A new family of primitive serphitoid wasps in ȱȱǻ ¢DZȱǼ Michael S. Engel1,2 Abstract.ȱ ȱ ȱ ȱ ¢ȱ ȱ ȱ ȱ ǻDZȱ Ǽȱ ȱ ȱ ȱ ęȱȱArchaeoserphitidae Engel, new family. The family is based on Archaeoserphites melqartiȱǰȱ ȱȱȱǰȱȱȱ¢ȱȱȱȱǰȱ ȱȱ ȱȱȱ ȬǰȱȱǯȱȱArchaeoserphites have several ȱȱȱȱȱǻe.gǯǰȱȱǰȱȱȱ¢ȱDzȱ ȱȱȱȱĚDzȱȱȱȱǼǰȱ ȱ¢ȱ¡ȱȱ ȱȱȱǻe.gǯǰȱȱ ȱǰȱ ȱ¢ȱ DzȱȱDzȱ ȱDzȱȱǼǯȱȱȱȱȱ¢ȱȱȱȱ¡ȱȱȱȱ ǰȱȱȱ¢ȱMicroserphitinaeȱǰȱ ȱ¢ǰȱȱǯ ȱȱȱȱȱȱȱȱȱȱ ȱ ¢ȱ ȱ Ȧ¢ȱ ¢ǰȱ ȱ ȱ ¢ȱ ȱ ȱ ȱ ȱȱǻ ȱǭȱǰȱŘŖŖśǼǯȱȱȱȱȱȱȱȬ ȱȱȱȱȱǰȱ¢ȱȱȱ¢ȱȱ¢ȱ ȱȱȱȱȱȱȱȱȱȱȱȱȱȱ ǻe.gǯǰȱ ǰȱŗşŝřDzȱ ǰȱŗşŞŜDzȱȱǭȱ ǰȱŘŖŖŚǰȱŘŖŖŜǰȱŘŖŖŝǰȱŘŖŗřDzȱǰȱ ŘŖŖřǰȱŘŖŖśǰȱŘŖŖŜǰȱŘŖŖŞDzȱȱet alǯǰȱŘŖŗřǰȱŘŖŗřDzȱȱet alǯǰȱŘŖŖŝDzȱȱǭȱǰȱŘŖŖŞDzȱ ȱet alǯǰȱŘŖŖşDzȱȬȱet alǯǰȱŘŖŖşǰȱŘŖŗŗǰȱŘŖŗŗǰȱŘŖŗŚDzȱÛȱet alǯǰȱŘŖŗŖDzȱ 1ȱȱȱ¢ǰȱȱ ¢ȱǰȱȱȱȱ¢ȱǭȱȬ ¢ȱ¢ǰȱŗśŖŗȱȱȱȮȱȱŗŚŖǰȱ¢ȱȱ ǰȱ ǰȱ ȱŜŜŖŚśȬ ŚŚŗśǰȱȱǻȓǯǼǯ 2ȱȱȱ ȱ¢ǰȱȱȱȱȱ ¢ǰȱȱȱȱȱ ŝşthȱǰȱ ȱǰȱ ȱȱŗŖŖŘŚȬśŗşŘǰȱǯ DZȱĴDZȦȦ¡ǯǯȦŗŖǯŗŝŗŜŗȦǯŖŗřǯśŖŜŚ Copyright © M.S. Engel. ȱȱĴȬȬȱŚǯŖȱ ȱǻȱȬȬȱŚǯŖǼǯ ȱŘřŘşȬśŞŞŖ 2 Novitates Paleoentomologicae No. 13 McKellar & Engel, 2012; McKellar et al., 2013; Olmi et al., 2014). Nonetheless, there are a series of distinctive extinct families that are almost hallmarks of the Cretaceous, representing apparently monophyletic groups that did not persist into the Cenozoic and were perhaps dwindling long before the Mesozoic came to its climactic closure. Each can be assigned to a superfamily and associated with their modern cousins, and inform us of the early branching events within these groups and of putatively ground- plan features aiding phylogenetic studies through the -
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. -
Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea
Biodiversity Data Journal 4: e8013 doi: 10.3897/BDJ.4.e8013 Taxonomic Paper Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea Natalie Dale-Skey‡, Richard R. Askew§‡, John S. Noyes , Laurence Livermore‡, Gavin R. Broad | ‡ The Natural History Museum, London, United Kingdom § private address, France, France | The Natural History Museum, London, London, United Kingdom Corresponding author: Gavin R. Broad ([email protected]) Academic editor: Pavel Stoev Received: 02 Feb 2016 | Accepted: 05 May 2016 | Published: 06 Jun 2016 Citation: Dale-Skey N, Askew R, Noyes J, Livermore L, Broad G (2016) Checklist of British and Irish Hymenoptera - Chalcidoidea and Mymarommatoidea. Biodiversity Data Journal 4: e8013. doi: 10.3897/ BDJ.4.e8013 Abstract Background A revised checklist of the British and Irish Chalcidoidea and Mymarommatoidea substantially updates the previous comprehensive checklist, dating from 1978. Country level data (i.e. occurrence in England, Scotland, Wales, Ireland and the Isle of Man) is reported where known. New information A total of 1754 British and Irish Chalcidoidea species represents a 22% increase on the number of British species known in 1978. Keywords Chalcidoidea, Mymarommatoidea, fauna. © Dale-Skey N et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 2 Dale-Skey N et al. Introduction This paper continues the series of checklists of the Hymenoptera of Britain and Ireland, starting with Broad and Livermore (2014a), Broad and Livermore (2014b) and Liston et al. -
Phylogeny of the Hymenoptera: a Cladistic Reanalysis of Rasnitsyn's (1988) Data
Phylogeny of the Hymenoptera: A cladistic reanalysis of Rasnitsyn's (1988) data FREDRIK RONQUIST,ALEXANDR P. RASNITSYN,ALAIN ROY,KATARINA ERIKSSON &MAGNUS LINDGREN Accepted: 26 April 1999 Ronquist, F., Rasnitsyn, A. P., Roy, A., Eriksson, K. & Lindgren, M. (1999) Phylogeny of the Hymenoptera: A cladistic reanalysis of Rasnitsyn's (1998) data. Ð Zoologica Scripta 28, 13±50. The hypothesis of higher-level relationships among extinct and extant hymenopterans presented by Rasnitsyn in 1988 is widely cited but the evidence has never been presented in the form of a character matrix or analysed cladistically. We review Rasnitsyn's morphological work and derive a character matrix for fossil and recent hymenopterans from it. Parsimony analyses of this matrix under equal weights and implied weights show that there is little support for Rasnitsyn's biphyletic hypothesis, postulating a sister-group relationship between tenthredinoids and macroxyelines. Instead, the data favour the conventional view that Hymenoptera excluding the Xyelidae are monophyletic. Higher- level symphytan relationships are well resolved and, except for the basal branchings, largely agree with the tree presented by Rasnitsyn. There is little convincing support for any major divisions of the Apocrita but the Microhymenoptera and the Ichneumonoidea + Aculeata appear as monophyletic groups in some analyses and require only a few extra steps in the others. The Evaniomorpha appear as a paraphyletic grade of basal apocritan lineages and enforcing monophyly of this grouping requires a considerable increase in tree length. The Ceraphronoidea are placed in the Proctotrupomorpha, close to Chalcidoidea and Platygastroidea. This signal is not entirely due to loss characters that may have evolved independently in these taxa in response to a general reduction in size. -
ON Frankliniella Occidentalis (Pergande) and Frankliniella Bispinosa (Morgan) in SWEET PEPPER
DIFFERENTIAL PREDATION BY Orius insidiosus (Say) ON Frankliniella occidentalis (Pergande) AND Frankliniella bispinosa (Morgan) IN SWEET PEPPER By SCOT MICHAEL WARING A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENT FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2005 ACKNOWLEDGMENTS I thank my Mom for getting me interested in what nature has to offer: birds, rats, snakes, bugs and fishing; she influenced me far more than anyone else to get me where I am today. I thank my Dad for his relentless support and concern. I thank my son, Sequoya, for his constant inspiration and patience uncommon for a boy his age. I thank my wife, Anna, for her endless supply of energy and love. I thank my grandmother, Mimi, for all of her love, support and encouragement. I thank Joe Funderburk and Stuart Reitz for continuing to support and encourage me in my most difficult times. I thank Debbie Hall for guiding me and watching over me during my effort to bring this thesis to life. I thank Heather McAuslane for her generous lab support, use of her greenhouse and superior editing abilities. I thank Shane Hill for sharing his love of entomology and for being such a good friend. I thank Tim Forrest for introducing me to entomology. I thank Jim Nation and Grover Smart for their help navigating graduate school and the academics therein. I thank Byron Adams for generous use of his greenhouse and camera. I also thank (in no particular order) Aaron Weed, Jim Dunford, Katie Barbara, Erin Britton, Erin Gentry, Aissa Doumboya, Alison Neeley, Matthew Brightman, Scotty Long, Wade Davidson, Kelly Sims (Latsha), Jodi Avila, Matt Aubuchon, Emily Heffernan, Heather Smith, David Serrano, Susana Carrasco, Alejandro Arevalo and all of the other graduate students that kept me going and inspired about the work we have been doing. -
Changes to the Fossil Record of Insects Through Fifteen Years of Discovery
This is a repository copy of Changes to the Fossil Record of Insects through Fifteen Years of Discovery. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/88391/ Version: Published Version Article: Nicholson, David Blair, Mayhew, Peter John orcid.org/0000-0002-7346-6560 and Ross, Andrew J (2015) Changes to the Fossil Record of Insects through Fifteen Years of Discovery. PLosOne. e0128554. https://doi.org/10.1371/journal.pone.0128554 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ RESEARCH ARTICLE Changes to the Fossil Record of Insects through Fifteen Years of Discovery David B. Nicholson1,2¤*, Peter J. Mayhew1, Andrew J. Ross2 1 Department of Biology, University of York, York, United Kingdom, 2 Department of Natural Sciences, National Museum of Scotland, Edinburgh, United Kingdom ¤ Current address: Department of Earth Sciences, The Natural History Museum, London, United Kingdom * [email protected] Abstract The first and last occurrences of hexapod families in the fossil record are compiled from publications up to end-2009.