'The Dermaptera of Canada B Y E
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Taxonomy of Iberian Anisolabididae (Dermaptera)
Acta Zoologica Academiae Scientiarum Hungaricae 63(1), pp. 29–43, 2017 DOI: 10.17109/AZH.63.1.29.2017 TAXONOMY OF IBERIAN ANISOLABIDIDAE (DERMAPTERA) Mario García-París Museo Nacional de Ciencias Naturales, MNCN-CSIC c/José Gutiérrez Abascal, 2, 28006, Madrid. Spain. E-mail: [email protected] An update on the taxonomy and geographic distribution of Iberian Anisolabididae (Der- maptera) is provided. Former catalogues reported in the Iberian Peninsula three genera of Anisolabididae: Aborolabis, Anisolabis, and Euborellia. A revision of 487 specimens of Iberian and North African Anisolabidoidea permit to exclude the genus Aborolabis from the Iberian fauna, the re-assignation of inland Euborellia annulipes Iberian records to Euborellia moesta, and the exclusion of Aborolabis angulifera from Northwestern Africa. Examination of type materials of Aborolabis mordax and Aborolabis cerrobarjai allows to propose the treatment of A. cerrobarjai as a junior synonym of A. mordax. The diagnostic characters of Euborellia his- panica are included within the local variability found in E. moesta. I propose that E. hispanica should be treated as a junior synonym of E. moesta. Key words: earwigs, systematics, Mediterranean region, Spain, Morocco, NW Africa. INTRODUCTION The Iberian fauna of Dermaptera, including Anisolabididae Verhoeff, 1902, has been the subject of diverse revisionary (Bolívar 1876, 1897, Lapeira & Pascual 1980, Herrera Mesa 1980, Bivar de Sousa 1997) and compilatory works (Herrera Mesa 1999). These revisions together with the monograph of the Fauna of France (Albouy & Caussanel 1990) and the on-line information included in Fauna Europaea (Haas 2010), rendered the image of Dermaptera as a well known group in continental western Europe. -
Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence
When the Body Hides the Ancestry: Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence Petr Kocarek1*, Vaclav John2, Pavel Hulva2,3 1 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Ostrava, Czech Republic, 2 Department of Zoology, Faculty of Science, Charles University in Prague, Prague, Czech Republic, 3 Life Science Research Centre, Faculty of Science, University of Ostrava, Ostrava, Czech Republic Abstract Here, we present a study regarding the phylogenetic positions of two enigmatic earwig lineages whose unique phenotypic traits evolved in connection with ectoparasitic relationships with mammals. Extant earwigs (Dermaptera) have traditionally been divided into three suborders: the Hemimerina, Arixeniina, and Forficulina. While the Forficulina are typical, well-known, free-living earwigs, the Hemimerina and Arixeniina are unusual epizoic groups living on molossid bats (Arixeniina) or murid rodents (Hemimerina). The monophyly of both epizoic lineages is well established, but their relationship to the remainder of the Dermaptera is controversial because of their extremely modified morphology with paedomorphic features. We present phylogenetic analyses that include molecular data (18S and 28S ribosomal DNA and histone-3) for both Arixeniina and Hemimerina for the first time. This data set enabled us to apply a rigorous cladistics approach and to test competing hypotheses that were previously scattered in the literature. Our results demonstrate that Arixeniidae and Hemimeridae belong in the dermapteran suborder Neodermaptera, infraorder Epidermaptera, and superfamily Forficuloidea. The results support the sister group relationships of Arixeniidae+Chelisochidae and Hemimeridae+Forficulidae. This study demonstrates the potential for rapid and substantial macroevolutionary changes at the morphological level as related to adaptive evolution, in this case linked to the utilization of a novel trophic niche based on an epizoic life strategy. -
The Genetic Mechanism of Selfishness and Altruism in Parent-Offspring Coadaptation Min Wu, Jean-Claude Walser, Lei Sun and Mathias Kölliker
SCIENCE ADVANCES | RESEARCH ARTICLE EVOLUTIONARY BIOLOGY Copyright © 2020 The Authors, some rights reserved; The genetic mechanism of selfishness and altruism exclusive licensee American Association in parent-offspring coadaptation for the Advancement Min Wu1*, Jean-Claude Walser2, Lei Sun3†, Mathias Kölliker1*‡ of Science. No claim to original U.S. Government Works. Distributed The social bond between parents and offspring is characterized by coadaptation and balance between altruistic under a Creative and selfish tendencies. However, its underlying genetic mechanism remains poorly understood. Using transcriptomic Commons Attribution screens in the subsocial European earwig, Forficula auricularia, we found the expression of more than 1600 genes License 4.0 (CC BY). associated with experimentally manipulated parenting. We identified two genes, Th and PebIII, each showing evidence of differential coexpression between treatments in mothers and their offspring. In vivo RNAi experiments confirmed direct and indirect genetic effects of Th and PebIII on behavior and fitness, including maternal food provisioning and reproduction, and offspring development and survival. The direction of the effects consistently indicated a reciprocally altruistic function for Th and a reciprocally selfish function for PebIII. Further metabolic pathway analyses suggested roles for Th-restricted endogenous dopaminergic reward, PebIII-mediated chemical communication and a link to insulin signaling, juvenile hormone, and vitellogenin in parent-offspring Downloaded from coadaptation and social evolution. INTRODUCTION manipulations with and without mother-offspring contact, without Parents and offspring influence each other’s behavior and evolutionary detrimental effects on offspring. Females produce one or two clutches http://advances.sciencemag.org/ fitness through reciprocal interactions (1). As an altruistic trait, over their lifetime and provide food (see movie S1) and protection parental care is beneficial to the survival and development of offspring to their young nymphs (8, 9). -
1. Padil Species Factsheet Scientific Name: Common Name Image
1. PaDIL Species Factsheet Scientific Name: Doru taeniatum (Dohrn, 1862) (Dermaptera: Forficulidae: Forficulinae) Common Name Earwig Live link: http://www.padil.gov.au/maf-border/Pest/Main/140292 Image Library New Zealand Biosecurity Live link: http://www.padil.gov.au/maf-border/ Partners for New Zealand Biosecurity image library Landcare Research — Manaaki Whenua http://www.landcareresearch.co.nz/ MPI (Ministry for Primary Industries) http://www.biosecurity.govt.nz/ 2. Species Information 2.1. Details Specimen Contact: MAF Plant Health & Environment Laboratory - [email protected] Author: MAF Plant Health & Environment Laboratory Citation: MAF Plant Health & Environment Laboratory (2010) Earwig(Doru taeniatum)Updated on 3/23/2014 Available online: PaDIL - http://www.padil.gov.au Image Use: Free for use under the Creative Commons Attribution-NonCommercial 4.0 International (CC BY- NC 4.0) 2.2. URL Live link: http://www.padil.gov.au/maf-border/Pest/Main/140292 2.3. Facets Groups: Earwigs Commodity Overview: Horticulture Commodity Type: Mango Status: NZ - Exotic Pest Status: 0 Unknown Distribution: 0 Unknown Host Family: 0 Unknown 2.4. Other Names Apterygida taeniata Bormans & Krauss, 1900 Forficula californica Dohrn, 1865 Forficula exilis Scudder, 1876 Forficula taeniata Dohrn, 1862 Sphingolabis californica Bormans, 1893 2.5. Diagnostic Notes **Adult** General colour deep black and bright yellow; 4th antennal segment more than twice as long as broad; pronotum transverse; tegmina and wings always fully developed; tegminae yellow with brown inner margins; hindwings visible beyond tegminae; 2nd tarsal segments dilated and much wider than 3rd, extending conspicuously beneath 3rd. Male pygidium elongate, posteriorly produced into a spine. Forceps typical, slightly arcuate; widely seperated at base. -
Big Wigs and Small Wigs: the Roles of Size, Sex and Shelter in Spatial Distribution Patterns in the Maritime Earwig Anisolabis Maritima
Big wigs and small wigs: the roles of size, sex and shelter in spatial distribution patterns in the maritime earwig Anisolabis maritima Nicole Hack1,2, Vikram Iyengar¹,3 Blinks/NSF REU/BEACON 2013 Summer 2013 Contact Information: Nicole Hack Ecology and Evolutionary Biology Department University of California Santa Cruz 1156 High St. Santa Cruz, CA 95064 [email protected] Keywords: Anisolabis maritima, maritime earwig, cohabitation, sex and size 1 Friday Harbor Laboratories, University of Washington, Friday Harbor, Washington 98250 2 Department of Ecology and Evolutionary Biology, University of California Santa Cruz, Santa Cruz, CA 95064 3 Department of Biology, Villanova University, Villanova, PA 19085 Hack 1 Abstract Animal aggregations can occur for a variety of abiotic factors, such as resource limitation, or biotic factors including sexual selection and predator-prey interactions. Although it is challenging to determine the underlying mechanism of such grouping behavior, we conducted experiments in which we examined the interactions and distribution patterns among pairs of the maritime earwig Anisolabis maritima (Order Dermaptera). This insect, found in aggregations under beach debris around the world, is sexually dimorphic regarding its most distinctive feature in that females have straight posterior forceps/pinchers whereas males have asymmetrical, curved forceps. We placed pairs of individuals varying in sex and size and monitored their distribution with and without shelter at 15 min, 12 h and 24 h to determine the roles that these factors may play in spatial patterns and gain insight into the mating system. Overall, we found that females were less likely to cohabitate than males, and they were more tolerant of males than other females. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Earwigs from Brazilian Caves, with Notes on the Taxonomic and Nomenclatural Problems of the Dermaptera (Insecta)
A peer-reviewed open-access journal ZooKeys 713: 25–52 (2017) Cave-dwelling earwigs of Brazil 25 doi: 10.3897/zookeys.713.15118 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Earwigs from Brazilian caves, with notes on the taxonomic and nomenclatural problems of the Dermaptera (Insecta) Yoshitaka Kamimura1, Rodrigo L. Ferreira2 1 Department of Biology, Keio University, 4-1-1 Hiyoshi, Yokohama 223-8521, Japan 2 Center of Studies in Subterranean Biology, Biology Department, Federal University of Lavras, CEP 37200-000 Lavras (MG), Brazil Corresponding author: Yoshitaka Kamimura ([email protected]) Academic editor: Y. Mutafchiev | Received 17 July 2017 | Accepted 19 September 2017 | Published 2 November 2017 http://zoobank.org/1552B2A9-DC99-4845-92CF-E68920C8427E Citation: Kamimura Y, Ferreira RL (2017) Earwigs from Brazilian caves, with notes on the taxonomic and nomenclatural problems of the Dermaptera (Insecta). ZooKeys 713: 25–52. https://doi.org/10.3897/zookeys.713.15118 Abstract Based on samples collected during surveys of Brazilian cave fauna, seven earwig species are reported: Cy- lindrogaster cavernicola Kamimura, sp. n., Cylindrogaster sp. 1, Cylindrogaster sp. 2, Euborellia janeirensis, Euborellia brasiliensis, Paralabellula dorsalis, and Doru luteipes, as well as four species identified to the (sub) family level. To date, C. cavernicola Kamimura, sp. n. has been recorded only from cave habitats (but near entrances), whereas the other four organisms identified at the species level have also been recorded from non-cave habitats. Wings and female genital structures of Cylindrogaster spp. (Cylindrogastrinae) are examined for the first time. The genital traits, including the gonapophyses of the 8th abdominal segment shorter than those of the 9th segement, and venation of the hind wings of Cylindrogastrinae correspond to those of the members of Diplatyidae and not to Pygidicranidae. -
Alteration of Gut Microbiota with a Broad-Spectrum Antibiotic Does Not Impair Maternal Care in the European Earwig
bioRxiv preprint doi: https://doi.org/10.1101/2020.10.08.331363; this version posted February 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Alteration of gut microbiota with a broad-spectrum antibiotic does not impair 2 maternal care in the European earwig. 3 Sophie Van Meyel*, Séverine Devers, Simon Dupont, Franck Dedeine and Joël Meunier 4 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261 CNRS – Université de Tours, Tours, 5 France 6 *Corresponding author: S. Van Meyel, [email protected] bioRxiv preprint doi: https://doi.org/10.1101/2020.10.08.331363; this version posted February 10, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. ABSTRACT 7 The microbes residing within the gut of an animal host often increase their own fitness by 8 modifying their host’s physiological, reproductive, and behavioural functions. Whereas recent 9 studies suggest that they may also shape host sociality and therefore have critical effects on 10 animal social evolution, the impact of the gut microbiota on maternal care remains unexplored. 11 This is surprising, as this behaviour is widespread among animals, often determines the fitness 12 of both juveniles and parents, and is essential in the evolution of complex animal societies. -
European Earwig, Forficula Auricularia Linnaeus (Insecta: Dermaptera: Forficulidae)1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-032 European Earwig, Forficula auricularia Linnaeus (Insecta: Dermaptera: Forficulidae)1 H. V. Weems, Jr., and P. E. Skelley2 Introduction Distribution The European earwig, Forficula auricularia This earwig is found throughout Europe, but it Linnaeus 1758, is intercepted in Florida frequently in seldom is present in great numbers. Quantities of bundles of plants and shrubbery, in cut flowers, and nursery stock arrive from the western United States in florists' equipment arriving from the western annually that are infested with this earwig, but it has United States. This insect is spread largely by man. not successfully established in Florida. While it has Spread by natural means is limited because earwigs not been considered of great economic importance in seldom fly and cannot maintain flight very long. It Europe, it has become a serious pest in parts of the has not yet become established in Florida, but it has United States. the potential to do so, at least in the northern part of the state. This earwig was recorded first in the United The European earwig is widespread in cooler States at Newport, Rhode Island in 1911 (Jones parts of the world. Originally known from the 1917). Jones (1917) reported a small colony from Palearctic Region, the European earwig has been Seattle, Washington in 1915. Later evidence indicated recorded from Canada (British Columbia, Manitoba, that it first invaded North America somewhere on the Newfoundland, Nova Scotia, Ontario, Quebec, and west coast in the early 1900s. Eventually it became Saskatchewan) and the United States (Arizona, widespread in the New England and Middle Atlantic California, Colorado, Idaho, Maine, Massachusetts, states and throughout most of the western states, Montana, New York, North Carolina, Oregon, Rhode especially where there is abundant rainfall or Island, Utah, and Washington). -
Summer 2012 Bulletin of the Oregon Entomological Society
Summer 2012 Bulletin of the Oregon Entomological Society Dragonfly Pond Watch—coming to a wetland near you! Celeste Mazzacano1 Dragonfly Migration Although dragonfly migration has been documented for over 100 years, there is still much to be learned, as we lack defini- Dragonfly migration is one of the most fascinating events in the tive answers to questions surrounding the environmental cues insect world, but also one of the least-known. This is even more that trigger migration, the adaptive advantages gained by the surprising when you consider that dragonfly migration occurs on subset of odonate species that migrate, reproductive activity of every continent except Antarctica. When people think of insect migration, the Monarch butterfly (Danaus plexippus) is a familiar figure, but the Wandering Glider (Pantala flavescens), a widely distributed species also known as a regular mi- grant in North America, can travel 11,000 miles (17,700 km) across the Indian Ocean from Africa to India and back—more than twice the distance of the Monarch’s well-known annual journey. Only about 16 of our 326 dragonfly species in North America are regular migrants, with some making annual seasonal flights while others are more sporadic. The major migratory species in North America are Common Green Darner (Anax junius), Wandering Glider (Pantala flave- scens), Spot-winged Glider (P. hymenaea), Black Saddlebags (Tramea lacerata), and Variegated Meadowhawk (Sympetrum corruptum). Different species tend to dominate migration flights in different parts of the continent. Anax junius is our best-known migrant, moving in Common Green Darner (Anax junius) at North Bend, Coos County, Oregon. -
Dermaptera (Insecta), Identified by A. Brindle and Preserved in the Collections of the National Museum of Natural History (Sofia)
Historia naturalis bulgarica, 21: 211-213, 2015 Dermaptera (Insecta), identified by A. Brindle and preserved in the collections of the National Museum of Natural History (Sofia) Petar Beron Abstract: The National Museum of Natural history in Sofia stores a collection of 30 species of earwigs (Dermaptera) from Nepal, Sri Lanka, Nigeria and other countries, identified by A. Brindle 30 years ago. Many other Dermaptera (unidentified) are also housed at the museum. Key Words: Dermaptera, Museum, Nepal, Nigeria, Sri Lanka, Brindle In the 1970s I contacted Dr. Alan Brindle Sardinia, North Korea, Vietnam, the Dominican (Manchester) who agreed to identify the collection Republic, Peru, Brazil, Bolivia, Papua New Guinea, of Dermaptera, brought by me from many countries DR Congo, Zambia, Zimbabwe, Mozambique, (Nigeria, Cameroon, Equatorial Guinea, Canary Nigeria, Tanzania, Uganda, Sudan, and the Balkan Islands, Tanzania, DR Congo, Nepal, Burma, countries. This list does not include the entire Thailand, Sri Lanka, Bolivia, Brazil, Peru, Papua Dermaptera material of the Museum, as there are New Guinea and others) and preserved now in the also many earwigs from Bulgaria and the Balkans National Museum of Natural History in Sofia. Dr. identified by other specialists. Brindle (1915 – 2001) was one of the leading world As the identifications by Dr. Brindle were done specialists in Dermaptera. Despite his retirement in by 1985, I tried to actualize the names taking into 1982, he tried to work also on part of our collection account the changes meanwhile. and returned most of the material in Sofia. He Abbreviations: P.B. – Petar Beron, S.A. – Stoitse published one new species from Nigeria (Diplatys Andreev, V.B. -
THE EARWIGS of CALIFORNIA (Order Dermaptera)
BULLETIN OF THE CALIFORNIA INSECT SURVEY VOLUME 20 THE EARWIGS OF CALIFORNIA (Order Dermaptera) BY ROBERT L. LANGSTON and J. A. POWELL UNIVERSITY OF CALIFORNIA PRESS THE EARWIGS OF CALIFORNIA (Order Dermaptera) BULLETIN OF THE CALIFORNIA INSECT SURVEY VOLUME 20 THE EARWIGS OF CALIFORNIA (Order Dermaptera) BY ROBERT L. LANGSTON and J. A. POWELL UNIVERSITY OF CALIFORNIA PRESS BERKELEY LOS ANGELES LONDON 1975 BULLETIN OF THE CALIFORNIA INSECT SURVEY Advisory Editors: H. V. Daly, J. A. Powell; J. N. Belkin, R. M. Bohart, R. L. Doutt, D. P. Furman, J. D. Pinto, E. I. Schlinger, R. W. Thorp VOLUME 20 Approved for publication September 20,1974 Issued August 15, 1975 UNIVERSITY OF CALIFORNIA PRESS BERKELEY AND LOS ANGELES UNIVERSITY OF CALIFORNIA PRESS, LTD. LONDON, ENGLAND ISBN 0-520-09524-3 LIBRARY OF CONGRESS CATALOG CARD NUMBER: 74-22940 0 1975 BY THE REGENTS OF THE UNIVERSITY OF CALIFORNIA PRINTED BY OFFSET IN THE UNITED STATES OF AMERICA CONTENTS Introduction .................................................. 1 California fauna ............................................. 1 Biology ................................................... 1 History of establishment and spread of introduced species in California ........ 2 Analysis of data ............................................. 4 Acknowledgments ............................................ 4 Systematic Treatment Classification ............................................... 6 Key to California species ........................................ 6 Anisolabis maritima (Ght5) ...................................