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Insect Orders
CMG GardenNotes #313 Insect Orders Outline Anoplura: sucking lice, page 1 Blattaria: cockroaches and woodroaches, page 2 Coleoptera: beetles, page 2 Collembola: springtails, page 4 Dermaptera: earwigs, page 4 Diptera: flies, page 5 Ephemeroptera: mayflies, page 6 Hemiptera (suborder Heteroptera): true bugs, page 7 Hemiptera (suborders Auchenorrhyncha and Sternorrhyncha): aphids, cicadas, leafhoppers, mealybugs, scale and whiteflies, page 8 Hymenoptera: ants, bees, horntails, sawflies, and wasp, page 9 Isoptera: termites, page 11 Lepidoptera: butterflies and moths, page 12 Mallophaga: chewing and biting lice, page 13 Mantodea: mantids, page 14 Neuroptera: antlions, lacewings, snakeflies and dobsonflies, page 14 Odonata: dragonflies and damselflies, page 15 Orthoptera: crickets, grasshoppers, and katydids, page 15 Phasmida: Walking sticks, page 16 Plecoptera: stoneflies, page 16 Psocoptera: Psocids or booklice, page 17 Siphonaptera: Fleas, page 17 Thysanoptera: Thrips, page 17 Trichoptera: Caddisflies, page 18 Zygentomaa: Silverfish and Firebrats, page 18 Anoplura Sucking Lice • Feeds by sucking blood from mammals. • Some species (head lice and crabs lice) feed on humans. Metamorphosis: Simple/Gradual Features: [Figure 1] Figure 1. Sucking lice o Wingless o Mouthparts: Piercing/sucking, designed to feed on blood. o Body: Small head with larger, pear-shaped thorax and nine segmented abdomen. 313-1 Blattaria (Subclass of Dictyoptera) Cockroaches and Woodroaches • Most species are found in warmer subtropical to tropical climates. • The German, Oriental and American cockroach are indoor pests. • Woodroaches live outdoors feeding on decaying bark and other debris. Metamorphosis: Simple/Gradual Figure 2. American cockroach Features: [Figure 2] o Body: Flattened o Antennae: Long, thread-like o Mouthparts: Chewing o Wings: If present, are thickened, semi-transparent with distinct veins and lay flat. -
Genomes of the Hymenoptera Michael G
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Digital Repository @ Iowa State University Ecology, Evolution and Organismal Biology Ecology, Evolution and Organismal Biology Publications 2-2018 Genomes of the Hymenoptera Michael G. Branstetter U.S. Department of Agriculture Anna K. Childers U.S. Department of Agriculture Diana Cox-Foster U.S. Department of Agriculture Keith R. Hopper U.S. Department of Agriculture Karen M. Kapheim Utah State University See next page for additional authors Follow this and additional works at: https://lib.dr.iastate.edu/eeob_ag_pubs Part of the Behavior and Ethology Commons, Entomology Commons, and the Genetics and Genomics Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ eeob_ag_pubs/269. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Ecology, Evolution and Organismal Biology at Iowa State University Digital Repository. It has been accepted for inclusion in Ecology, Evolution and Organismal Biology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Genomes of the Hymenoptera Abstract Hymenoptera is the second-most sequenced arthropod order, with 52 publically archived genomes (71 with ants, reviewed elsewhere), however these genomes do not capture the breadth of this very diverse order (Figure 1, Table 1). These sequenced genomes represent only 15 of the 97 extant families. Although at least 55 other genomes are in progress in an additional 11 families (see Table 2), stinging wasps represent 35 (67%) of the available and 42 (76%) of the in progress genomes. -
Mitochondrial Phylogenomics of Tenthredinidae (Hymenoptera: Tenthredinoidea) Supports the Monophyly of Megabelesesinae As a Subfamily
insects Article Mitochondrial Phylogenomics of Tenthredinidae (Hymenoptera: Tenthredinoidea) Supports the Monophyly of Megabelesesinae as a Subfamily Gengyun Niu 1,†, Sijia Jiang 2,†, Özgül Do˘gan 3 , Ertan Mahir Korkmaz 3 , Mahir Budak 3 , Duo Wu 1 and Meicai Wei 1,* 1 College of Life Sciences, Jiangxi Normal University, Nanchang 330022, China; [email protected] (G.N.); [email protected] (D.W.) 2 College of Forestry, Beijing Forestry University, Beijing 100083, China; [email protected] 3 Department of Molecular Biology and Genetics, Faculty of Science, Sivas Cumhuriyet University, Sivas 58140, Turkey; [email protected] (Ö.D.); [email protected] (M.B.); [email protected] (E.M.K.) * Correspondence: [email protected] † These authors contributed equally to this work. Simple Summary: Tenthredinidae is the most speciose family of the paraphyletic ancestral grade Symphyta, including mainly phytophagous lineages. The subfamilial classification of this family has long been problematic with respect to their monophyly and/or phylogenetic placements. This article reports four complete sawfly mitogenomes of Cladiucha punctata, C. magnoliae, Megabeleses magnoliae, and M. liriodendrovorax for the first time. To investigate the mitogenome characteristics of Tenthredinidae, we also compare them with the previously reported tenthredinid mitogenomes. To Citation: Niu, G.; Jiang, S.; Do˘gan, Ö.; explore the phylogenetic placements of these four species within this ecologically and economically Korkmaz, E.M.; Budak, M.; Wu, D.; Wei, important -
An Unusual New Lineage of Sawflies (Hymenoptera) in Upper Cretaceous Amber from Northern Myanmar
Cretaceous Research 60 (2016) 281e286 Contents lists available at ScienceDirect Cretaceous Research journal homepage: www.elsevier.com/locate/CretRes An unusual new lineage of sawflies (Hymenoptera) in Upper Cretaceous amber from northern Myanmar * Michael S. Engel a, b, , Diying Huang c, Abdulaziz S. Alqarni d, Chenyang Cai c a Division of Entomology, Natural History Museum, 1501 Crestline Drive e Suite 140, University of Kansas, Lawrence, KS 66045-4415, USA b Department of Ecology & Evolutionary Biology, University of Kansas, Lawrence, KS 66045, USA c State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, People's Republic of China d Department of Plant Protection, College of Food and Agriculture Sciences, King Saud University, P.O. Box 2460, Riyadh 11451, Saudi Arabia article info abstract Article history: A peculiar new lineage of sawflies (‘Symphyta’) is described and figured from a female beautifully pre- Received 22 October 2015 served in Upper Cretaceous (Cenomanian) amber from northern Myanmar. Syspastoxyela rhaphidia Engel Received in revised form and Huang, gen. et sp. nov., shares many plesiomorphic features with the primitive Xyelidae, 22 December 2015 yXyelotomidae, and yXyelydidae such as enlarged and thickened first flagellomere succeeded by a series Accepted in revised form 26 December 2015 of thinner and shorter flagellomeres, absence of a transverse mesoscutal sulcus, multiple preapical spurs, Available online 12 January 2016 and two protibial spurs among other traits. However, the new lineage has an apomorphically contracted forewing venation, lacks a subcostal vein, has a single marginal cell, and lacks crossvein 1r-rs, and thus it Keywords: fi Burmese amber is segregated into a new family, Syspastoxyelidae Engel and Huang, fam. -
Subfamily Composition of Ichneumonidae (Hymenoptera) from Western Amazonia: Insights Into Diversity of Tropical Parasitoid Wasps
Insect Conservation and Diversity (2012) doi: 10.1111/j.1752-4598.2012.00185.x Subfamily composition of Ichneumonidae (Hymenoptera) from western Amazonia: Insights into diversity of tropical parasitoid wasps ANU VEIJALAINEN,1 ILARI E. SA¨ A¨ KSJA¨ RVI,1 TERRY L. ERWIN,2 1 3 ISRRAEL C. GO´ MEZ and JOHN T. LONGINO 1Department of Biology, Section of Biodi- versity and Environmental Science, University of Turku, Turku, Finland, 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, USA and 3Department of Biology, University of Utah, Salt Lake City, UT, USA Abstract. 1. Previous studies have found the parasitoid wasp family Ichneumonidae (Hymenoptera) to have an exceptional latitudinal species richness gradient that peaks at mid-latitudes instead of the tropics; however, insufficient tropical sampling and species description may have biased the conclusions. It has been unclear which subfamilies might be species rich in tropical lowland rain forests. 2. This study reports the subfamily abundance composition of a large ichneumo- nid data set (>30 000 individuals in 20 subfamilies) collected by Malaise traps and insecticidal canopy fogging in Amazonian Ecuador and Peru and suggests which subfamilies would be important for future study. 3. Relative abundance data from one Peruvian site are compared to similar low- land samples from Costa Rica and Georgia (USA). 4. Contrary to a common assumption, a number of ichneumonid subfamilies are very abundant and presumably species rich in western Amazonia. Cryptinae and Or- thocentrinae are noticeably the two most abundant subfamilies, and a number of koinobiont lepidopteran parasitoids, which are generally thought to be scarce in the tropics, are also surprisingly abundant (e.g. -
Evolution of the Insects
CY501-C11[407-467].qxd 3/2/05 12:56 PM Page 407 quark11 Quark11:Desktop Folder:CY501-Grimaldi:Quark_files: But, for the point of wisdom, I would choose to Know the mind that stirs Between the wings of Bees and building wasps. –George Eliot, The Spanish Gypsy 11HHymenoptera:ymenoptera: Ants, Bees, and Ants,Other Wasps Bees, and The order Hymenoptera comprises one of the four “hyperdi- various times between the Late Permian and Early Triassic. verse” insectO lineages;ther the others – Diptera, Lepidoptera, Wasps and, Thus, unlike some of the basal holometabolan orders, the of course, Coleoptera – are also holometabolous. Among Hymenoptera have a relatively recent origin, first appearing holometabolans, Hymenoptera is perhaps the most difficult in the Late Triassic. Since the Triassic, the Hymenoptera have to place in a phylogenetic framework, excepting the enig- truly come into their own, having radiated extensively in the matic twisted-wings, order Strepsiptera. Hymenoptera are Jurassic, again in the Cretaceous, and again (within certain morphologically isolated among orders of Holometabola, family-level lineages) during the Tertiary. The hymenopteran consisting of a complex mixture of primitive traits and bauplan, in both structure and function, has been tremen- numerous autapomorphies, leaving little evidence to which dously successful. group they are most closely related. Present evidence indi- While the beetles today boast the largest number of cates that the Holometabola can be organized into two major species among all orders, Hymenoptera may eventually rival lineages: the Coleoptera ϩ Neuropterida and the Panorpida. or even surpass the diversity of coleopterans (Kristensen, It is to the Panorpida that the Hymenoptera appear to be 1999a; Grissell, 1999). -
A Maple Wood Wasp, Xiphydria Maculata, and Its Insect Enemies (Hymenoptera: Xiphydriiade)
The Great Lakes Entomologist Volume 17 Number 1 - Spring 1984 Number 1 - Spring 1984 Article 3 April 1984 A Maple Wood Wasp, Xiphydria Maculata, and its Insect Enemies (Hymenoptera: Xiphydriiade) Mark A. Deyrup Archbold Biological Station Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Deyrup, Mark A. 1984. "A Maple Wood Wasp, Xiphydria Maculata, and its Insect Enemies (Hymenoptera: Xiphydriiade)," The Great Lakes Entomologist, vol 17 (1) Available at: https://scholar.valpo.edu/tgle/vol17/iss1/3 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Deyrup: A Maple Wood Wasp, <i>Xiphydria Maculata,</i> and its Insect Enem 1984 THE GREAT LAKES ENTOMOLOGIST 17 A MAPLE WOOD WASP, XIPHYDRIA MACULATA, AND ITS INSECT ENEMIES (HYMENOPTERA: XIPHYDRIIADE) Mark A. Deyrupl ABSTRACT A xiphydriid wood wasp, Xiphydria mandata, is very common in branches ofAeer spp. in Indiana. and is frequently the proximate cause of branches falling from shade trees. X. maculata is attacked by seven parasitoids: Alliaells bllrquei (Aulacidae), A. digitalis, Rhyssella nitida (Ichneumonidae), Xiphydriophagus meyer/llcki! (Pteromalidae), Co· eloides TOssiclls betlltae (Braconidae), Spathills elegans (Braconidae), and OruSSlIs sp. (Orussidae). The latter three parasitoids prior to this study had no confirmed hosts; Xiphydriophagus is new to N. America. This parasitoid complex is compared with that of the Palaearctic Xiphydria camelus, showing a series of pairs of closely related Palaearctic and :\earctic forms. -
Evidence for UV-Green Dichromacy in the Basal Hymenopteran Sirex Noctilio
www.nature.com/scientificreports OPEN Evidence for UV‑green dichromacy in the basal hymenopteran Sirex noctilio (Siricidae) Quentin Guignard 1*, Johannes Spaethe 2, Bernard Slippers 3, Martin Strube‑Bloss 2,5 & Jeremy D. Allison 1,4 A precondition for colour vision is the presence of at least two spectral types of photoreceptors in the eye. The order Hymenoptera is traditionally divided into the Apocrita (ants, bees, wasps) and the Symphyta (sawfies, woodwasps, horntails). Most apocritan species possess three diferent photoreceptor types. In contrast, physiological studies in the Symphyta have reported one to four photoreceptor types. To better understand the evolution of photoreceptor diversity in the Hymenoptera, we studied the Symphyta Sirex noctilio, which belongs to the superfamily Siricoidea, a closely related group of the Apocrita suborder. Our aim was to (i) identify the photoreceptor types of the compound eye by electroretinography (ERG), (ii) characterise the visual opsin genes of S. noctilio by genomic comparisons and phylogenetic analyses and (iii) analyse opsin mRNA expression. ERG measurements revealed two photoreceptor types in the compound eye, maximally sensitive to 527 and 364 nm. In addition, we identifed three opsins in the genome, homologous to the hymenopteran green or long‑wavelength sensitive (LW) LW1, LW2 and ultra‑violet sensitive (UV) opsin genes. The LW1 and UV opsins were found to be expressed in the compound eyes, and LW2 and UV opsins in the ocelli. The lack of a blue or short‑wavelength sensitive (SW) homologous opsin gene and a corresponding receptor suggests that S. noctilio is a UV‑green dichromate. Te ability to see colours, i.e. -
Ent20 3 265 271 Gokhman.P65
Russian Entomol. J. 20(3): 265271 © RUSSIAN ENTOMOLOGICAL JOURNAL, 2011 Morphotypes of chromosome sets and pathways of karyotype evolution of parasitic Hymenoptera Ìîðôîëîãè÷åñêèå òèïû õðîìîñîìíûõ íàáîðîâ è íàïðàâëåíèÿ ýâîëþöèè êàðèîòèïà ïàðàçèòè÷åñêèõ ïåðåïîí÷àòîêðûëûõ (Hymenoptera) V.E. Gokhman Â.Å. Ãîõìàí Botanical Garden, Moscow State University, Moscow 119991, Russia. E-mail: [email protected] Áîòàíè÷åñêèé ñàä Ìîñêîâñêîãî ãîñóäàðñòâåííîãî óíèâåðñèòåòà, Ìîñêâà 119991, Ðîññèÿ. KEY WORDS: chromosomes, karyotype evolution, morphotypes, parasitic Hymenoptera. ÊËÞ×ÅÂÛÅ ÑËÎÂÀ: õðîìîñîìû, ýâîëþöèÿ êàðèîòèïà, ìîðôîëîãè÷åñêèå òèïû, ïàðàçèòè÷åñêèå ïåðåïîí÷àòîêðûëûå. ABSTRACT. Chromosomal diversity of parasitic ly ants [Imai et al., 1988; Hoshiba, Imai, 1993]. Fur- Hymenoptera has been analyzed with the help of the thermore, karyotypes, or rather karyomes (term intro- logical possibility space approach. Using three param- duced by Smirnov [1991]), usually evolve as holistic eters (haploid chromosome number, length ratios of objects [Lukhtanov, 1999] (see also Rasnitsyn, 1987), chromosomes within the haploid set, and the degree of and construction of the so-called chromosomal alter- karyotypic metacentricity), 18 classes, or morpho- ation networks [Imai, 1991, 1993], an apparent tool logical types, of chromosome sets have been delimited, proposed for analysis of karyotype evolution in many of which only 13 contain at least one karyotype. Possi- groups of living organisms including Hymenoptera, is ble major pathways of karyotypic transformation in probably unable to describe this process in an adequate parasitic wasps have been outlined. manner. The main aim of the present paper is therefore a thorough analysis of the major morphotypes and path- ÐÅÇÞÌÅ. Õðîìîñîìíîå ðàçíîîáðàçèå ïàðàçè- ways of karyotypic transformation in parasitic Hy- òè÷åñêèõ Hymenoptera ïðîàíàëèçèðîâàíî ñ ïîìî- menoptera. -
Morphology and Function of the Ovipositor Mechanism in Ceraphronoidea
JHR 33: 25–61 (2013)Morphology and function of the ovipositor mechanism in Ceraphronoidea... 25 doi: 10.3897/JHR.33.5204 RESEARCH ARTICLE www.pensoft.net/journals/jhr Morphology and function of the ovipositor mechanism in Ceraphronoidea (Hymenoptera, Apocrita) Andrew F. Ernst1, István Mikó1,2, Andrew R. Deans1,2 1 North Carolina State University, Department of Entomology, Raleigh, NC 27695-7613 USA 2 Pennsylva- nia State University, Department of Entomology, 501 ASI Building, University Park, PA 16802 USA Corresponding author: István Mikó ([email protected]) Academic editor: M. Yoder | Received 25 March 2013 | Accepted 4 July 2013 | Published 1 August 2013 Citation: Ernst AF, István Mikó I, Deans AR (2013) Morphology and function of the ovipositor mechanism in Ceraphronoidea (Hymenoptera, Apocrita). Journal of Hymenoptera Research 33: 25–61. doi: 10.3897/JHR.33.5204 Abstract The ovipositor of apocritan Hymenoptera is an invaluable source of phylogenetically relevant characters, and our understanding of its functional morphology stands to enlighten us about parasitoid life history strategies. Although Ceraphronoidea is one of the most commonly collected Hymenoptera taxa with considerable economic importance, our knowledge about their natural history and phylogenetic relation- ships, both to other apocritan lineages and within the superfamily itself, is limited. As a first step towards revealing ceraphronoid natural diversity we describe the skeletomuscular system of the ceraphronoid ovi- positor for the first time. Dissections and Confocal Laser Scanning Microscopy 3D media files were used to visualize the ovipositor complex and to develop character concepts. Morphological structures were described in natural language and then translated into a character-character state format, whose terminol- ogy was linked to phenotype-relevant ontologies. -
Ichnews 11, October 1988
~_EfilCAN ENTOMOLOGICAL )NSTITUTE ICB~~W~~ Editor: Michael Sharkey, Hiosystematics Research centre, r ~qriculture Canada, C.E.F., Ottawa, Ontario, KlA OC6, Canada. ~lternate Editors: Paul Marsh uavl4 Wahl £ntomol091Cal Lab., USUA, American £ntomolo91cal Institute c/o u.s. Nationa l Mu seurt~ 300~ Sll ~6th ~ve. llashlnqton. D.C .• 20~60 Gainesville. Florida, 32608 U.S.A. U.S.A. EDITORIAL This is getting ridiculous; here it is the end of 1988 and the 1987 Ichnews is just getting out. I'm not sure who to blame but if I can find anyone besides myself I'll let you know . I have enclosed with this issue the questionnaire for Ichnews 1988. The prompt return of this questionnaire should ensure that the next issue is published before March 1, 1988. Please return these to Paul Marsh before February 1, as he is the next editor. Speaking about enigmas, I have a little quiz for our readers. To what family does the specimen illustrated above belong? Those who answer correctly will get the next two issues of ICHNEWS absolutely free. We would like to know if there are any other topics that are of general interest to our readers. The questionnaire on wing venation nomenclature seemed to elicit a good response (thanks for the suggestion Bob Wharton), what next? Many of us had the opportunity to meet this July in Vancouver on the occasion of the XVIII International congress Of Entomology. Most agree that it was a success, especially those who found out about Wreck Beach! The Internation society Of Hymenopterist's met and announced the new executive: President, (our own) Paul Marsh; Vice President, z. -
A Generic Classification of the Nearctic Sawflies (Hymenoptera, Symphyta)
THE UNIVERSITY OF ILLINOIS LIBRARY rL_L_ 5 - V. c_op- 2 CD 00 < ' sturn this book on or before the itest Date stamped below. A arge is made on all overdue oks. University of Illinois Library UL28: .952 &i;g4 1952 %Po S IQ";^ 'APR 1 1953 DFn 7 W54 '•> d ^r-. ''/./'ji. Lit]—H41 Digitized by tine Internet Arciiive in 2011 with funding from University of Illinois Urbana-Champaign http://www.archive.org/details/genericclassific15ross ILLINOIS BIOLOGICAL MONOGRAPHS Vol. XV No. 2 Published by the University of Illinois Under the Auspices of the Graduate School Ukbana, Illinois 1937 EDITORIAL COMMITTEE John Theodore Buchholz Fred Wilbur Tanner Harley Jones Van Cleave UNIVERSITY OF ILLINOIS 1000—7-37—11700 ,. PRESS A GENERIC CLASSIFICATION OF THE NEARCTIC SAWFLIES (HYMENOPTERA, SYMPHYTA) WITH SEVENTEEN PLATES BY Herbert H. Ross Contribution No. 188 from the Entomological Laboratories of the University of Illinois, in Cooperation with the Illinois State Natural History Survey CONTENTS Introduction 7 Methods 7 Materials 8 Morphology 9 Head and Appendages 9 Thorax and Appendages 22 Abdomen and Appendages 29 Phylogeny 33 The Superfamilies of Sawflies 33 Family Groupings 34 Hypothesis of Genealogy .... 35 Larval Characters 45 - Biology 46 Summary of Phylogeny 48 Taxonomy 50 Superfamily Tenthredinoidea 51 Superfamily Megalodontoidea 106 Superfamily Siricoidea 110 Superfamily Cephoidea 114 Bibliography 117 Plates 127 Index 162 ACKNOWLEDGMENT This monograph is an elaboration of a thesis sub- mitted in partial fulfillment for the degree of Doctor of Philosophy in Entomology in the Graduate School of the University of Illinois in 1933. The work was done under the direction of Dr.