Um Método De Armazenamento Para Psocoptera (Insecta: Psocodea) Em Caixa De CD
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Fossil Record of Stem Groups Employed In
www.nature.com/scientificreports OPEN Fossil record of stem groups employed in evaluating the chronogram of insects (Arthropoda: Received: 07 April 2016 Accepted: 16 November 2016 Hexapoda) Published: 13 December 2016 Yan-hui Wang1,2,*, Michael S. Engel3,*, José A. Rafael4,*, Hao-yang Wu2, Dávid Rédei2, Qiang Xie2, Gang Wang1, Xiao-guang Liu1 & Wen-jun Bu2 Insecta s. str. (=Ectognatha), comprise the largest and most diversified group of living organisms, accounting for roughly half of the biodiversity on Earth. Understanding insect relationships and the specific time intervals for their episodes of radiation and extinction are critical to any comprehensive perspective on evolutionary events. Although some deeper nodes have been resolved congruently, the complete evolution of insects has remained obscure due to the lack of direct fossil evidence. Besides, various evolutionary phases of insects and the corresponding driving forces of diversification remain to be recognized. In this study, a comprehensive sample of all insect orders was used to reconstruct their phylogenetic relationships and estimate deep divergences. The phylogenetic relationships of insect orders were congruently recovered by Bayesian inference and maximum likelihood analyses. A complete timescale of divergences based on an uncorrelated log-normal relaxed clock model was established among all lineages of winged insects. The inferred timescale for various nodes are congruent with major historical events including the increase of atmospheric oxygen in the Late Silurian and earliest Devonian, the radiation of vascular plants in the Devonian, and with the available fossil record of the stem groups to various insect lineages in the Devonian and Carboniferous. Over half of all described living species are insects, and they dominate all terrestrial ecosystems1. -
Phylogeny of Endopterygote Insects, the Most Successful Lineage of Living Organisms*
REVIEW Eur. J. Entomol. 96: 237-253, 1999 ISSN 1210-5759 Phylogeny of endopterygote insects, the most successful lineage of living organisms* N iels P. KRISTENSEN Zoological Museum, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen 0, Denmark; e-mail: [email protected] Key words. Insecta, Endopterygota, Holometabola, phylogeny, diversification modes, Megaloptera, Raphidioptera, Neuroptera, Coleóptera, Strepsiptera, Díptera, Mecoptera, Siphonaptera, Trichoptera, Lepidoptera, Hymenoptera Abstract. The monophyly of the Endopterygota is supported primarily by the specialized larva without external wing buds and with degradable eyes, as well as by the quiescence of the last immature (pupal) stage; a specialized morphology of the latter is not an en dopterygote groundplan trait. There is weak support for the basal endopterygote splitting event being between a Neuropterida + Co leóptera clade and a Mecopterida + Hymenoptera clade; a fully sclerotized sitophore plate in the adult is a newly recognized possible groundplan autapomorphy of the latter. The molecular evidence for a Strepsiptera + Díptera clade is differently interpreted by advo cates of parsimony and maximum likelihood analyses of sequence data, and the morphological evidence for the monophyly of this clade is ambiguous. The basal diversification patterns within the principal endopterygote clades (“orders”) are succinctly reviewed. The truly species-rich clades are almost consistently quite subordinate. The identification of “key innovations” promoting evolution -
Evolution of the Insects David Grimaldi and Michael S
Cambridge University Press 0521821495 - Evolution of the Insects David Grimaldi and Michael S. Engel Index More information INDEX 12S rDNA, 32, 228, 269 Aenetus, 557 91; general, 57; inclusions, 57; menageries 16S rDNA, 32, 60, 237, 249, 269 Aenigmatiinae, 536 in, 56; Mexican, 55; parasitism in, 57; 18S rDNA, 32, 60, 61, 158, 228, 274, 275, 285, Aenne, 489 preservation in, 58; resinite, 55; sub-fossil 304, 307, 335, 360, 366, 369, 395, 399, 402, Aeolothripidae, 284, 285, 286 resin, 57; symbioses in, 303; taphonomy, 468, 475 Aeshnoidea, 187 57 28S rDNA, 32, 158, 278, 402, 468, 475, 522, 526 African rock crawlers (see Ambermantis wozniaki, 259 Mantophasmatodea) Amblycera, 274, 278 A Afroclinocera, 630 Amblyoponini, 446, 490 aardvark, 638 Agaonidae, 573, 616: fossil, 423 Amblypygida, 99, 104, 105: in amber, 104 abdomen: function, 131; structure, 131–136 Agaoninae, 423 Amborella trichopoda, 613, 620 Abies, 410 Agassiz, Alexander, 26 Ameghinoia, 450, 632 Abrocomophagidae, 274 Agathiphaga, 560 Ameletopsidae, 628 Acacia, 283 Agathiphagidae, 561, 562, 567, 630 American Museum of Natural History, 26, 87, acalyptrate Diptera: ecological diversity, 540; Agathis, 76 91 taxonomy, 540 Agelaia, 439 Amesiginae, 630 Acanthocnemidae, 391 ages, using fossils, 37–39; using DNA, 38–40 ametaboly, 331 Acari, 99, 105–107: diversity, 101, fossils, 53, Ageniellini, 435 amino acids: racemization, 61 105–107; in-Cretaceous amber, 105, 106 Aglaspidida, 99 ammonites, 63, 642 Aceraceae, 413 Aglia, 582 Amorphoscelidae, 254, 257 Acerentomoidea, 113 Agrias, 600 Amphientomidae, -
Wettability and Contaminability of Insect Wings As a Function of Their Surface Sculptures
Acta Zoologica (Stockholm), Vol. 77, No. 3. pp. 213-225, 1996 Pergamon Copyright © 1996 The Royal Swedish Academy of Sciences Published by Elsevier Science Ltd Printed in Great Britain. All rights reserved 0001-7272/96 $15.00-1- .00 0001-7272(95)00017-8 Wettability and Contaminability of Insect Wings as a Function of Their Surface Sculptures Thomas Wagner, Christoph Neinhuis and Wilhelm Barthlott Botanisches Institut und Botanischer Ganen der Universitat Bonn, Meckenheimer Allee 170, D-53! 15 Bonn, Germany (Accepted for publication 15 July 1995) Abstract Wagner, T, Neinhuis, C. & Barthlott, W. 1996. Wettability and contaminability of insect wings as a function of their surface sculptures. Acta Zoologica (Stockholm) 76: 21.3-225. The wing surfaces of 97 insect species from vinually all relevant major groups were examined by high resolution scanning-electron-microscopy, in order to identify the relationships between the wing microstructures, their wettability with water and their behaviour under the influence of con- tamination. Isolated wings with contact angles between 31.6° and 155.5° were anificially contaminated with silicate dusts and subsequently fogged until drops of water ("dew") formed and rolled off. The remaining panicles were counted via a digital image analysis system. Remaining panicle values between 0.41% and 103% were determined in companson with unfogged controls. Some insects with very unwettable wings show a highly significant "self-cleaning" effect under the infiuence of rain or dew. Detailed analysis revealed that there is a correlation between the wettability and the "SM Index" (quotient of wing surfaceAbody mass)"''') with values ranging from 2.42 to 57.0. -
Evolution of the Insects
CY501-C08[261-330].qxd 2/15/05 11:10 PM Page 261 quark11 27B:CY501:Chapters:Chapter-08: 8 TheThe Paraneopteran Orders Paraneopteran The evolutionary history of the Paraneoptera – the bark lice, fold their wings rooflike at rest over the abdomen, but thrips true lice, thrips,Orders and hemipterans – is a history beautifully and Heteroptera fold them flat over the abdomen, which reflected in structure and function of their mouthparts. There probably relates to the structure of axillary sclerites and other is a general trend from the most generalized “picking” minute structures at the base of the wing (i.e., Yoshizawa and mouthparts of Psocoptera with standard insect mandibles, Saigusa, 2001). to the probing and puncturing mouthparts of thrips and Relationships among paraneopteran orders have been anopluran lice, and the distinctive piercing-sucking rostrum discussed by Seeger (1975, 1979), Kristensen (1975, 1991), or beak of the Hemiptera. Their mouthparts also reflect Hennig (1981), Wheeler et al. (2001), and most recently by diverse feeding habits (Figures 8.1, 8.2, Table 8.1). Basal Yoshizawa and Saigusa (2001). These studies generally agree paraneopterans – psocopterans and some basal thrips – are on the monophyly of the order Hemiptera and most of its microbial surface feeders. Thysanoptera and Hemiptera suborders and a close relationship of the true lice (order independently evolved a diet of plant fluids, but ancestral Phthiraptera) with the most basal group, the “bark lice” (Pso- heteropterans were, like basal living families, predatory coptera), which comprise the Psocodea. One major issue is insects that suction hemolymph and liquified tissues out of the position of thrips (order Thysanoptera), which either their prey. -
Phylogenomics and the Evolution of Hemipteroid Insects
Phylogenomics and the evolution of hemipteroid insects Kevin P. Johnsona,1, Christopher H. Dietricha, Frank Friedrichb, Rolf G. Beutelc, Benjamin Wipflerc,d, Ralph S. Petersd, Julie M. Allena,e, Malte Petersenf, Alexander Donathf, Kimberly K. O. Waldeng, Alexey M. Kozlovh, Lars Podsiadlowskif,i, Christoph Mayerf, Karen Meusemannf,j,k, Alexandros Vasilikopoulosf, Robert M. Waterhousel, Stephen L. Cameronm, Christiane Weirauchn, Daniel R. Swansona, Diana M. Percyo,p, Nate B. Hardyq, Irene Terryr, Shanlin Lius, Xin Zhout, Bernhard Misoff, Hugh M. Robertsong, and Kazunori Yoshizawau aIllinois Natural History Survey, Prairie Research Institute, University of Illinois at Urbana–Champaign, Champaign, IL 61820; bInstitut für Zoologie, Universität Hamburg, 20146 Hamburg, Germany; cInstitut für Zoologie und Evolutionsforschung, Friedrich-Schiller-Universität Jena, 07743 Jena, Germany; dCenter of Taxonomy and Evolutionary Research, Arthropoda Department, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; eDepartment of Biology, University of Nevada, Reno, NV 89557; fCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; gDepartment of Entomology, University of Illinois at Urbana–Champaign, Urbana, IL 61801; hScientific Computing Group, Heidelberg Institute for Theoretical Studies, 69118 Heidelberg, Germany; iInstitute of Evolutionary Biology and Ecology, University of Bonn, 53121 Bonn, Germany; jEvolutionary Biology and Ecology, Institute for Biology I (Zoology), University of -
Ametabolous & Hemimetabolous Orders
Ametabolous & Hemimetabolous orders Collembola • Springtails • Minute, most common in soil & leaf litter samples. • Lack wings or obvious mouthparts. • Interesting ‘springtail’ mechanism: tenaculum + furcula. • Often blue/purplish color. Archaeognatha • Bristletails • Large eyes, wingless, external mouthparts. • Arched back, long middle terminal filament. • Covered with scales. Zygentoma/Thysanura • Silverfish & firebrats. • Very small eyes, dorsoventrally flattened, lack wings. • Lateral filaments same length or longer than middle. • Also covered with scales. Hemimetabolous orders Ephemeroptera Odonata Dragonflies (Anisoptera) & Damselflies (Zygoptera) • Sister taxon to Neoptera. • No winged molts. • 6000 species worldwide • Aquatic naiads • Predaceous adults Hemimetabolous orders ORTHOPTERA: Grasshoppers, locusts, katydids, crickets • Largest clade of Polyneoptera: 20,000 species worldwide. • Distinctive saltatory (jumping) hindlegs. • Prothorax large and shield-like. • Two monophyletic suborders: Caelifera and Ensifera. Caelifera • Grasshoppers and locusts • Day-active, fast- moving, visually acute, terrestrial herbivores Ensifera • Katydids • Crickets • Mormon crickets, • Jerusalem crickets • wetas • Cooloola monsters. • Often night-active, camouflaged or mimetic, predators, omnivores, or phytophages. The other Polyneoptera The Dictuoptera/Dictyoptera Mantodea Blattodea Blattodea Blattodea Termitoidae Isoptera Dermaptera Phasmatodea The Paraneoptera Psocoptera • Booklice & Barklice Phthiraptera • Chewing & Sucking lice The Hemiptera -
Insect Orders III: Paraneoptera
Insect Orders III: Paraneoptera • The group Paraneoptera consists of 4 insect orders, the bark lice, true lice, thrips and hemipterans. The Paraneoptera is clearly monophyletic based on morphological and molecular evidence. • The evolutionary history of the Paraneoptera is a history beautifully reflected in structure and function of their mouthparts. • The mouthparts of the Paraneoptera also reflect diverse feeding habits. Basal groups are microbial surface feeders, whereas more advanced groups feed on plant fluids (phloem) or animal fluids (blood). Modification of mouthparts in the Paraneoptera • Mouthparts in the Paraneoptera show a striking evolutionary trend from the most generalized “picking” mouthparts of the Psocoptera with standard insect mandibles to the probing and puncturing mouthparts of thrips and anopluran lice and the distinctive piercing-sucking rostrum or beak of the Hemiptera. • In these evolutionary transitions the mandibles become greatly reduced and modified. The laciniae of the maxilla, in contrast, become enlarged and modified and together with the mandibles form the stylets of the Hemiptera. Psocoptera (Bark lice) • Classification. 4,400 described species arranged into 3 suborders (Trogiomorpha, Troctomorpha and Psocomorpha) with 50 families and over 200 genera. First insect order to show the beginnings of a transition to sucking mouthparts. Sister group to the Phthiraptera (the lice). • Structure. Lacinia of the maxilla is modified from the dentate form in orthopteroids into an elongate rod-like structure, proximately sunken well into the head capsule. The hind coxa of most psocopterans has a Pearman’s organ with an adjacent tympanum that is suppose to be stridulatory. Postclypeus on the face is budging as are the eyes. -
Taxonomy & Systema`Cs
Taxonomy & Systemacs • These give us the background to understand the evoluon of: – Morphology – Physiology – Ecology – Life History – Geography – Etc. What are they? • Taxonomy? • Systemacs? The goals of systemacs… • Determining relaonships • Understanding evoluonary history • Describing biodiversity • This is an incredibly challenging enterprise! Why? • It is primarily an historical and inferenal science. • Relaonships become obscured as me passes. Ancestry • Regardless, evoluonary history makes us what we are today. – 50,000 years of Homo sapiens – 4-6 my as homonids – 12-18 my as great apes – 85 my as primates – 125 my as eutherians – 210 my as mammals – 525 my as vertebrates Arthropod Ancestry • Insects are shaped by 400 my of history (as insects) as well. • But now we have to sort out (who knows how many?) millions of species. The earliest known insect fossil, Rhyniognatha hirsti Phylogenecs • Systemasts group taxa Class Insecta based on the principle of Order 1 descent with Family A Family B Genus A modificaon. 1 Genus B1 Genus A Genus B • Sort taxa into a hierarchy 2 2 Genus A of Orders, Families, and 3 Genus B3 Genera. Order 2 Family C Family D Genus C1 Genus D1 Genus C2 Genus D2 Genus C3 Genus D3 Phylogenecs Genus A1 • Systemasts group Genus A2 taxa based on the Family A Order 1 principle of descent Genus A3 with modificaon. Genus B1 • Sort taxa into a Genus B2 hierarchy of Orders, Family B Genus B Family, and Genera. 3 Genus C • The goal is to 1 construct these so Genus C2 that this hierarchy Family C Order 2 Genus C reflects evoluonary 3 Genus D1 history. -
Herbivory Increases Diversification Across Insect Clades
ARTICLE Received 26 Feb 2015 | Accepted 13 Aug 2015 | Published 24 Sep 2015 DOI: 10.1038/ncomms9370 OPEN Herbivory increases diversification across insect clades John J. Wiens1, Richard T. Lapoint1 & Noah K. Whiteman1 Insects contain more than half of all living species, but the causes of their remarkable diversity remain poorly understood. Many authors have suggested that herbivory has accelerated diversification in many insect clades. However, others have questioned the role of herbivory in insect diversification. Here, we test the relationships between herbivory and insect diversification across multiple scales. We find a strong, positive relationship between herbivory and diversification among insect orders. However, herbivory explains less variation in diversification within some orders (Diptera, Hemiptera) or shows no significant relation- ship with diversification in others (Coleoptera, Hymenoptera, Orthoptera). Thus, we support the overall importance of herbivory for insect diversification, but also show that its impacts can vary across scales and clades. In summary, our results illuminate the causes of species richness patterns in a group containing most living species, and show the importance of ecological impacts on diversification in explaining the diversity of life. 1 Department of Ecology and Evolutionary Biology, University of Arizona, 1041 E. Lowell Street, BioSciences West 310, Tucson, Arizona 85721, USA. Correspondence and requests for materials should be addressed to J.J.W. (email: [email protected]) or to N.K.W. (email: -
Based on Mitochondrial Genomes
See discussions, stats, and author profiles for this publication at: http://www.researchgate.net/publication/236260264 Phylogenomics of Hemiptera (Insecta: Paraneoptera) based on mitochondrial genomes ARTICLE in SYSTEMATIC ENTOMOLOGY · JANUARY 2013 Impact Factor: 2.55 · DOI: 10.1111/j.1365-3113.2012.00660.x CITATIONS DOWNLOADS VIEWS 8 74 130 9 AUTHORS, INCLUDING: Qiang Xie Jianfu Zhou Nankai University Dartmouth College 18 PUBLICATIONS 285 CITATIONS 6 PUBLICATIONS 36 CITATIONS SEE PROFILE SEE PROFILE Xiaoguang Liu Wenjun Bu Nankai Univrsity Nankai University 62 PUBLICATIONS 118 CITATIONS 44 PUBLICATIONS 340 CITATIONS SEE PROFILE SEE PROFILE Available from: Kai Dang Retrieved on: 17 August 2015 Systematic Entomology (2013), 38, 233–245 DOI: 10.1111/j.1365-3113.2012.00660.x Phylogenomics of Hemiptera (Insecta: Paraneoptera) based on mitochondrial genomes ∗ ∗ ∗ YING CUI1 , QIANG XIE1 ,JIMENGHUA1 , KAI DANG1, JIANFU ZHOU2, XIAOGUANG LIU2, GANG WANG2,XINYU1 and W E N J U N B U1 1Institute of Entomology, College of Life Sciences, Nankai University, Tianjin, China and 2College of Information Technical Science, Nankai University, Tianjin, China Abstract. Hemiptera is the largest order in Paraneoptera and the fifth largest in Insecta. Disputes about hemipteran phylogeny have concerned the monophyly of Auchenorrhyncha and relationships between the suborders Fulgoromorpha, Cicado- morpha, Coleorrhyncha and Heteroptera. In a phylogenomic study of Hemiptera, we add two new mitochondrial genomes of Peloridiidae (Coleorrhyncha) to those reported in GenBank, to complete the taxon sampling of all suborders. We used two types of data – amino acid sequences and nucleotides of various combinations between protein coding genes, tRNAs and rRNAs – to infer the phylogeny of Hemiptera. -
Bibliographia Entomologica Austriaca 2003
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Entomologica Austriaca Jahr/Year: 2004 Band/Volume: 0011 Autor(en)/Author(s): Gepp Johannes, Körtvelyesi Daniela Artikel/Article: Bibliographia Entomologica Austriaca 2003. 11-20 © Österr. Ent. Ges. [ÖEG]/Austria; download unter www.biologiezentrum.at Entomologica Austriaca 11 / 2004 ÖEG Bibliographia Entomologica Austriaca 2003 Johannes Gepp & Daniela Körtvelyesi ALTENHOFER, E. & H. PSCHORN-WALCHER, 2003: Biologische Noti- Institut fur Naturschuz und Landschaftsökologie, zen über die Blattwespen-Gattungen Metallus Forbes, Steiermark, Heinrichstraße 5/3, A-8010 Graz; Monostegia A. Costa und Phymatocera Dahlbom (Hyme- [email protected]; Tel.: 0316/32606S Fax: 0316/326068-5 noptera: Tenthredinidae). - Linzer biol. Beitr., 35(1):405- 417. Die jährlich erscheinende Bibliographie berücksich- tigt entomologische Publikationen österreichischer ASPÖCK, H., 2003: 25 Jahre Österreichische Entomologische Gesellschaft. - In: GEPP, J. (Red.): Zur Geschichte der Ento- Autoren bzw. entomologische Publikationen über mologie in Österreich. Denisia, 8:279-319. Österreich. Sie entsteht durch Berücksichtigung der ASPÖCK, H., 2003: Durch Vektoren übertragene Parasiten. - 8. wesentlichen Zeitschriften der Bibliothek des Institu- Linzer Reisemedizinische Tagung, 15. März 2003: Ar- tes für Naturschutz in Graz sowie durch die Übermitt- thropoden und Infektionskrankheiten. Arbeitskreis Reise- lung von Zitatenlisten österreichischer Entomologen. medizin OÖ in Zusammenarbeit mit der Medizinischen Die Jahrgänge 1970 bis 1999 sind in 6 Beiheften Gesellschaft für Oberösterreich und der Österreichischen Gesellschaft für Reise- und Touristikmedizin (ASTTM), der „Berichte der Arbeitsgemeinschaft für ökologische Zusammenfassungen^ 4pp. Entomologie in Graz" publiziert, die Jahrgänge 2000 ASPÖCK, H., 2003: Erinnerungen an Dr. Klimesch (1902-1997). ff. jährlich in der vorliegenden Zeitschrift. - In: GEPP, J.