What Do Insects Do for a Living?
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
(Diptera: Bombyliidae), a Parasite of the Alkali Bee
Utah State University DigitalCommons@USU All PIRU Publications Pollinating Insects Research Unit 1960 The Biology of Heterostylum rubustum (Diptera: Bombyliidae), a Parasite of the Alkali Bee George E. Bohart Utah State University W. P. Stephen R. K. Eppley Follow this and additional works at: https://digitalcommons.usu.edu/piru_pubs Part of the Entomology Commons Recommended Citation Bohart, G. E., W. P. Stephen, and R. K. Eppley. 1960. The Biology of Heterostylum rubustum (Diptera: Bombyliidae), a Parasite of the Alkali Bee. Ann. Ent. Soc. Amer. 53(3): 425-435. This Article is brought to you for free and open access by the Pollinating Insects Research Unit at DigitalCommons@USU. It has been accepted for inclusion in All PIRU Publications by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. ( Reprinted from fu'<NALS OF THE ENTOMOLOGICAL SOCIETY OF rumRJCA Vol. 53, No. 3, May, 1960 THE BIOLOGY OF HETEROSTYLUM ROBUSTUM (DIPTERA: BOMBYLIIDAE), A PARASITE OF THE ALKALI BEE1 G . E. BOHART,' W. P. STEPHEN, Ai\ID R. K. EPPLEY3 ABSTRACT H eterostylum robustu m. (Osten Sacken) is the principal very brief second ins ta r, and a soft, helpless third ins tar , parasite of the a lkali bee (Nomia mela11deri Ckll.) in the to a tough, more active fourth instar. Some lat vae Northwestern States. It also parasitizes other species apparently mature on a single host, but others pa rt ially of Nomia and at least one species of both Nomadopsis and drain the fluids from a second as well. In the late Halictus. It eject-s eggs into and near the nest mounds summer or fall the mature larva makes an overwin tet ing of its host, but does not readily discr iminate between nest cell in the upper few inches of soil. -
Entomologia Experimentalis Et Applicata 150: 217–225, 2014 217 218 Murphy Et Al
DOI: 10.1111/eea.12155 Host ontogeny determines parasitoid use of a forest caterpillar Shannon M. Murphy1*, Teresa M. Stoepler2§, Kylee Grenis1 & John T. Lill2 1Department of Biological Sciences, University of Denver, Denver, CO, USA, and 2Department of Biological Sciences, George Washington University, Washington, DC, USA Accepted: 5 November 2013 Key words: complementary predation, niche partitioning, ontogenetic niche, size-structured parasitism, trophic interaction, Euclea delphinii,Limacodidae,Lepidoptera,Hymenoptera,Diptera Abstract For most organisms, patterns of natural enemy-mediated mortality change over the course of devel- opment. Shifts in enemy pressure are particularly relevant for organisms that exhibit exponential growth during development, such as juvenile insects that increase their mass by several orders of magnitude. As one of the dominant groups of insect herbivores in most terrestrial plant communi- ties, larval lepidopterans (caterpillars) are host to a diverse array of parasitoids. Previous research has described how the frequency of herbivore parasitism varies among host plants or habitats, but much less is known about how parasitism pressure changes during host development. To test whether the two major parasitoid taxa, wasps and flies, differentially attack shared hosts based on host develop- mental stage, we simultaneously exposed early- and late-instar Euclea delphinii Boisduval (Lepido- ptera: Limacodidae) caterpillars to parasitism in the field. We found strong evidence that parasitoids partition hosts by size; adult female wasps preferentially parasitized small caterpillars, whereas adult female flies preferred to attack large caterpillars. Our results demonstrate that host ontogeny is a major determinant of parasitoid host selection. Documenting how shifts in enemy pressure vary with development is important to understanding both the population biology and evolutionary ecology of prey species and their enemies. -
Arthropods of Public Health Significance in California
ARTHROPODS OF PUBLIC HEALTH SIGNIFICANCE IN CALIFORNIA California Department of Public Health Vector Control Technician Certification Training Manual Category C ARTHROPODS OF PUBLIC HEALTH SIGNIFICANCE IN CALIFORNIA Category C: Arthropods A Training Manual for Vector Control Technician’s Certification Examination Administered by the California Department of Health Services Edited by Richard P. Meyer, Ph.D. and Minoo B. Madon M V C A s s o c i a t i o n of C a l i f o r n i a MOSQUITO and VECTOR CONTROL ASSOCIATION of CALIFORNIA 660 J Street, Suite 480, Sacramento, CA 95814 Date of Publication - 2002 This is a publication of the MOSQUITO and VECTOR CONTROL ASSOCIATION of CALIFORNIA For other MVCAC publications or further informaiton, contact: MVCAC 660 J Street, Suite 480 Sacramento, CA 95814 Telephone: (916) 440-0826 Fax: (916) 442-4182 E-Mail: [email protected] Web Site: http://www.mvcac.org Copyright © MVCAC 2002. All rights reserved. ii Arthropods of Public Health Significance CONTENTS PREFACE ........................................................................................................................................ v DIRECTORY OF CONTRIBUTORS.............................................................................................. vii 1 EPIDEMIOLOGY OF VECTOR-BORNE DISEASES ..................................... Bruce F. Eldridge 1 2 FUNDAMENTALS OF ENTOMOLOGY.......................................................... Richard P. Meyer 11 3 COCKROACHES ........................................................................................... -
The Biodiversity and Systematics of the Entomophagous Parasitoid Strepsiptera (Insecta)
The Biodiversity and Systematics of the entomophagous parasitoid Strepsiptera (Insecta) Jeyaraney Kathirithamby, Department of Zoology and St Hugh’s College, Oxford. [email protected] [email protected] ABSTRACT Strepsiptera are small group of entomophagous parasiroids of cosmopolitan in distribution. They parasitize seven orders of Insecta and the common hosts in Europe are Hymenoptera, Hemiptera and Thysanura. INTRODUCTION Strepsiptera are obligate endoparasites the hosts of which include Blattodea, Diptera, Hemiptera, Hymenoptera, Mantodea, Orthoptera, and Thysanura, and 33 families. The name of the group is derived form the Greek words: twisted ( Strepsi-) and wing (pteron ), and refers in particular to the twisted hind wing of the male while in flight. Representatives of the suborder Mengenillidia show more primitive characteristics and parasitise Thysanura (Lepismatidae), the only known apterygote to be parasitized. Strepsiptera are cosmopolitan in distribution and are difficult to find: often the host has to be located to find the strepsipteran. To date about 600 species have been described, but many more await description and some could be cryptic species. The group is relatively well known in Europe (Kinzelbach, 1971, 1978), where details of Strepsiptera life history have been studied in Elenchus tenuicornis Kirby (Baumert, 1958, 1959), a parasite of Delphacidae (Homoptera) and in Xenos vesparum (Christ) (Hughes et al ., 2003, 2004a, 2004b, 2005), a parasite of polistine paper wasps (Hymenoptera: Vespidae). While most strepsipterans parasitize single taxa (leafhoppers or halictid bees), the males and females in the family Myrmecolacidae parasitize hosts belonging to different orders: (Formicidae and Orthoptera, respectively) (Ogloblin, 1939, Kathirithamby and Hamilton, 1992). -
23 BIOLOGY and HOST RELATIONSHIPS of PARASITOIDS Notes I
Parasitoid Biology 23 BIOLOGY AND HOST RELATIONSHIPS OF PARASITOIDS Notes I. Definitions of Parasitoid and Host A. Parasitoid: A parasitic insect that lives in or on and eventually kills a larger host insect (or other arthropod). B. Host: Those animals attacked by parasitoids. II. Characteristics of Parasitoids A. Parasitoids usually destroy their hosts during development. B. The parasitoid's host is usually in the same taxonomic class (Insecta). C. Parasitoids are large relative to their hosts. D. Parasitoid adults are freeliving while only the immature stages are parasitic. E. Parasitoids develop on only one host individual during the immature stages. F. With respect to population dynamics, parasitoids are similar to predatory insects. III. Mode of Development of Parasitoids A. With respect to the host 1. Endoparasitoid (internal): usually in situations where the host is exposed. 2. Ectoparasitoid (external): usually in situations where host lives within protected location (e.g., leafminers, in cocoons, under scale covers). B. With respect to numbers of immatures per individual host 1. Solitary parasitoid 2. Gregarious parasitoid C. With respect to host stage 1. Egg 2. Larvae 3. Pupa 4. Adult 5. Combinations of the above (i.e., egg-larval parasitoid) D. With respect to affect on host 1. Idiobionts: host development arrested or terminated upon parasitization (e.g., egg parasitoids) 2. Koinobionts: host continues to develop following parasitization (e.g., larval -pupal parasitoids) E. With respect to other parasitoid species 1. Primary parasitoid 2. Secondary parasitoid (Hyperparasitism) 3. Tertiary parasitoid (Hyperparasitism) Parasitoid Biology 24 Notes F. Competition among immature parasitoid stages 1. Intraspecific competition: Superparasitism 2. -
The History of the Systematic Placement of an Enigmatic Parasitic Insect Order H
Entomologia 2013; volume 1:e4 SYSTEMATICS AND PHYLOGENY The Strepsiptera-Odyssey: the history of the systematic placement of an enigmatic parasitic insect order H. Pohl, R.G. Beutel Friedrich-Schiller-University Jena, Germany Neuropterida. Several early hypotheses based on a typological Abstract approach − affinities with Diptera, Coleoptera, a coleopteran sub- group, or Neuropterida − were revived using either a Hennigian The history of the phylogenetic placement of the parasitic insect approach or formal analyses of morphological characters or different order Strepsiptera is outlined. The first species was described in molecular data sets. A phylogenomic approach finally supported a sis- 1793 by P. Rossi and assigned to the hymenopteran family tergroup relationship with monophyletic Coleoptera. Ichneumonidae. A position close to the cucujiform beetle family Rhipiphoridae was suggested by several earlier authors. Others pro- «Systemata entomologica perturbare videtur cum ex ordinibus posed a close relationship with Diptera or even a group Pupariata omnibus repellatur − animalculum − animum excrucians. Tempus including Diptera, Strepsiptera and Coccoidea. A subordinate place- ducamus, et dies alteri lucem afferent.» ment within the polyphagan series Cucujiformia close to the wood- [We see the entomological system confused, and that it (the associated Lymexylidae was favored by the coleopterist R.A. Crowson. strepsipteran) bounces out from all orders. The little critter gets W. Hennig considered a sistergroup relationship with Coleoptera as on our nerves. Time will show, and other days will bring light in the most likely hypothesis but emphasized the uncertainty. Cladistic this matter.] analyses of morphological data sets yielded very different place- ments, alternatively as sistergroup of Coleoptera, Antliophora, or all Latreille, 1809 other holometabolan orders. -
Figures in Italics Indicate the Prime Taxonomic Reference. Figures in Bold Type Indicate the Page on Which There Is a Figure. AB
INDEX Figures in italics indicate the prime taxonomic reference. Figures in bold type indicate the page on which there is a figure. ABALOOS, 732, 748 Acerentomon, food, 455, 4.59; A. Acrocera, 1006; A. globulus, ABEL, 49I, 493 doderoi, 455 1006 abdomen, Coleoptera, adephagid Acerentulus, 4.59; head, mouth Acroceridae, 10o6; larvae par type, haplogastrous, hologa parts, 456; internal anatomy, asitic, 970; mesopleural sulcus strous, symphiogastrous, 825, 457 straight, 979 826, Diptera, 864; Achanthiptera rohrellijormis Acromantis, 6oi Hymenoptera, number of ex ( = inanis) in nests of Vespula, Acronycta, larval ecdyses, I094 posed segments, I I 87 I249 Acrotelsa, 44I ABDULLAH,884,89I,904 Acherontia atropos, I I39; sound acrotrophic ovarioles, in ABERNATHY,722,756 production, I I40; larva, alimen Coleoptera, 832 Abies excelsa, Physokermes piceae, tary canal, 1095; mandibular Acrydiidae, see Tetrigidae a pest on, 726 gland, 267 Actaletes, 470; tracheae present, ABRAHAMSON,903,904 Acheta domesticus, 546, .5 48; 467 Abraxas grossulariata auditory organ, I33 Actaletidae, 470 (Geometridae) wing-variation, Achilidae, 705 Actinoscytidae, 762 1133 Achilixiidae, 70.5 ACTON,684,688,748,767 Acalyptratae, I 020; larvae oc achrestogonimes, in Isoptera, 620 Actora, see Helcomyza casionally parasitic, 970; ner ACHTELIG,426,427,794,8I2 Actornithophilus, 665 vous system, 970; preapical Achroia, I 12 I Aculagnathidae, 884 tibial bristle, 967 acid gland, 1189 Aculeata, see Hymenoptera Acanaloniidae, 707 Acidia, see Philophylla Aculeata acanthae, in Mecoptera, 936; in ACKER, 794, 812 aculei, in Lepidoptera, I077 Siphonaptera, 946 Aclerda, 729 Acyrtosiphon, 7I7; A. pisum, Acanthaspis, puncture by, pain Aclerdidae, 7 29 photoperiod, temperature and ful, 732 Acleris (Tortricidae) venation, wing-development, 722 Acanthiidae, see Cimicidae or 1708 ACZEL, IOI6, I02J, IOJ7, I046 Saldidae Acletoxenus, I022 ADAIR, 599, 601 Acanthoceridae, 86o Aclypea, 854 Adalia, colour variation, 882; Acanthococcus devoniensis, 728 Acraea, I 126 development oflarva, 883; A. -
Working Today for Nature Tomorrow
Report Number 583 The dotted bee-fly (Bombylius discolor Mikan 1796) A report on the survey and research work undertaken between 1999 and 2003 English Nature Research Reports working today for nature tomorrow English Nature Research Reports Number 583 The dotted bee-fly (Bombylius discolor mikan 1796) A report on the survey and research work undertaken between 1999 and 2003 David Gibbs You may reproduce as many additional copies of this report as you like, provided such copies stipulate that copyright remains with English Nature, Northminster House, Peterborough PE1 1UA ISSN 0967-876X © Copyright English Nature 2004 Acknowledgements During the survey work, research and data analysis I have relied on the help of many people. I would like to thank Esme Gilling of North Somerset Council for permission to do research at Uphill Quarry LNR and particularly Vina Bell, voluntary warden, for all her invaluable assistance. Also much appreciated was permission from Avon Wildlife Trust to do work at Hellenge Hill and I am especially grateful to Tim McGrath for this. Matthew Oates, Simon Hayhow (Larger Brachycera Recording Scheme), Rupert Higgins and Steve Falk all provided extra data on observations. Paul Westrich kindly did some pollen analysis. David Greathead provided copies of his papers on Bombylid biology and other information and advice. Summary • In four years of survey work from 1999-2003 70 sites were searched for B. discolor. • B. discolor was found at 36 sites, just over half. • Of these, 19 (53%) were proven to be breeding colonies (ie exuvia found) or shown to be very probable breeding colonies (ie oviposition observed). -
Diptera Families MS FINAL
The Diptera Families of British Columbia The Diptera Families of British Columbia G.G.E. Scudder and R.A. Cannings March 31, 2006 G.G.E. Scudder and R.A. Cannings Printed 04/25/06 Coleoptera Families of British Columbia Table of Contents Introduction......................................................................................................................................1 Order Diptera Description................................................................................................................3 Keys to Order Diptera and Families.................................................................................................6 Family Descriptions .......................................................................................................................26 Suborder NEMATOCERA............................................................................................................26 Infraorder TIPULOMORPHA .......................................................................................................26 Family TANYDERIDAE (Primitive Crane Flies) [Fig. 1]............................................................26 Family TIPULIDAE (Crane Flies) [Fig. 2]....................................................................................26 Infraorder BLEPHARICEROMORPHA .......................................................................................27 Family BLEPHARICERIDAE (Net-winged Midges) [Fig. 3]......................................................27 Family DEUTEROPHLEBIIDAE (Mountain -
Insecta: Strepsiptera) in Taimyr Upper Cretaceous Amber
Accepted Manuscript A putative twisted-wing parasitoid planidium (Insecta: Strepsiptera) in Taimyr Upper Cretaceous amber Jeyaraney Kathirithamby, Evgeny E. Perkovsky, Zachary H. Falin, Michael S. Engel PII: S0195-6671(16)30171-9 DOI: 10.1016/j.cretres.2016.08.010 Reference: YCRES 3440 To appear in: Cretaceous Research Received Date: 10 June 2016 Revised Date: 17 August 2016 Accepted Date: 17 August 2016 Please cite this article as: Kathirithamby, J., Perkovsky, E.E., Falin, Z.H., Engel, M.S., A putative twisted- wing parasitoid planidium (Insecta: Strepsiptera) in Taimyr Upper Cretaceous amber, Cretaceous Research (2016), doi: 10.1016/j.cretres.2016.08.010. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Cretaceous Research A putative twisted-wing parasitoid planidium (Insecta: Strepsiptera) in Taimyr Upper Cretaceous amber Jeyaraney Kathirithamby a, Evgeny E. Perkovsky b, Zachary H. Falin c, Michael S. Engel c,d,e a Department of Zoology, Oxford University, South Parks Road, Oxford OX1 3PS, United Kingdom ([email protected]). b Schmalhausen Institute of Zoology, National Academy of Sciences of Ukraine, 15 B. Khmelnitsky Street, Kiev 01-601, Ukraine ([email protected]). c Division of Entomology, Natural History Museum, 1501 Crestline Drive – Suite 140, University of Kansas, Lawrence, Kansas 66045-4415, USA ([email protected], [email protected]). -
Perspectives on Evolutionary and Developmental Biology
Festschrift 2 TheFestschrift series collects studies in honor of scientific personalities who have had a significant impact on research in their field. Editor in Chief Luca Illetterati With the sponsorship of First edition 2019, Padova University Press © 2019 Padova University Press Università degli Studi di Padova via 8 Febbraio 2, Padova www.padovauniversitypress.it ISBN 978-88-6938-140-9 Printed in January 2019 All rights reserved. For citations, graphics, cartographic and photographic reproductions belonging to the pro- perty of third parties included in this work, the publisher is available to the owner of the property we were unable to find, as well as for any unwanted omissions and/or attribution errors in references Perspectives on Evolutionary and Developmental Biology Essays for Alessandro Minelli edited by Giuseppe Fusco UPADOVA P Table of contents Contributors IX Preface XIII Part I Theoretical investigations The causal structure of development and its evolution 3 Wallace Arthur Towards a developmental biology of holobionts 13 Scott F. Gilbert An evolutionary biology for the 21st century 23 Armin P. Moczek Evo-devo’s challenges to the Modern Synthesis 29 Gerd B. Müller Ever since Darwin: Why plants are important for evo-devo research 41 Rolf Rutishauser Structural and dynamic approaches to the development and evolution of plant form 57 Rolf Sattler Part II Conceptual elaborations Homology and homoplasy of life cycle traits 71 James DiFrisco Objects or processes? Theoretical terms or frame-concepts? Coupled changes in the life sciences and in their epistemology 83 Elena Gagliasso Categories of developmental biology: Examples of ambiguities and how to deal with them 93 Joachim T. -
From Parasitoids to Gall Inducers and Inquilines
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 932 From Parasitoids to Gall Inducers and Inquilines Morphological Evolution in Cynipoid Wasps BY HEGE VÅRDAL ACTA UNIVERSITATIS UPSALIENSIS UPPSALA 2004 !""# $"%"" & ' & & ( ) * + ') ,- .) !""#) / ( 0 1 1 2 ) ' 3 ) 4 ) 56!) #$ ) ) 17 5$899#89: $8" ; & ' ' & + && & ) ' & & 6""" + ' + ' 2 <' & ' ' =) * & & & ' ' + & + & ) ( + ' ) & '' + & ' & ' 2 ) & ' ' '' & ' ' > '') * && & ' '' && '' > & ' '' + '' & ' '') / ' '' & > '' ) ' 8 & 6" & ' 2 ' + & & ) * + ? 66 ' &8 + & ) * ' ' + ' + & ' ) * ' ' & 2 ' + ' & + ) * + & 2 & ' & !9 & ) 1 & ' ' ) 3 &+ ' & ' ' ) 3 & & & + ' 8 ' ' > '') ; ' + & & '' & ' & ' @ ' + ' '') ' 2 ' ' !"# $ % # &# '() *+# # $,-./01 # A .' ,- !""# 17 $$"#8!6!B 17 5$899#89: $8" % %%% 865C9 < %DD )>)D E F % %%% 865C9= List of Papers This thesis is based on the following papers,