Temporal Activity of Spiders and Earwigs During Winter in Apple Trees
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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). -
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). -
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) ................................... -
Enhancing Biological Control in Apple Orchards Jaume Lordan Sanahuja
Enhancing biological control in apple orchards Jaume Lordan Sanahuja Dipòsit Legal: L.1233-2014 http ://hdl.handle.net/10803/275941 ADVERTIMENT. L'accés als continguts d'aquesta tesi doctoral i la seva utilització ha de respectar els drets de la persona autora. Pot ser utilitzada per a consulta o estudi personal, així com en activitats o materials d'investigació i docència en els termes establerts a l'art. 32 del Text Refós de la Llei de Propietat Intel·lectual (RDL 1/1996). Per altres utilitzacions es requereix l'autorització prèvia i expressa de la persona autora. En qualsevol cas, en la utilització dels seus continguts caldrà indicar de forma clara el nom i cognoms de la persona autora i el títol de la tesi doctoral. No s'autoritza la seva reproducció o altres formes d'explotació efectuades amb finalitats de lucre ni la seva comunicació pública des d'un lloc aliè al servei TDX. Tampoc s'autoritza la presentació del seu contingut en una finestra o marc aliè a TDX (framing). Aquesta reserva de drets afecta tant als continguts de la tesi com als seus resums i índexs. ADVERTENCIA. El acceso a los contenidos de esta tesis doctoral y su utilización debe respetar los derechos de la persona autora. Puede ser utilizada para consulta o estudio personal, así como en actividades o materiales de investigación y docencia en los términos establecidos en el art. 32 del Texto Refundido de la Ley de Propiedad Intelectual (RDL 1/1996). Para otros usos se requiere la autorización previa y expresa de la persona autora. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Connecticut State Entomologist . Thirty Ninth Report for 1939
Bulletin 434 June, 1940 LONNECTICUT STATEENTOMOLOGIST THIRTY -NINTH REPORT 1939 R. B. FRIEND, PH.D. State Entomologist Bulletin 434 June, 1940 CONNECTTCUTSTATE ENTOMOLOGIST THIRTY-NIP JTH R EPORT 19-.1.39 R. B. FRIEND, PH.1 State Entomologist CONTENTS ~NSECT~ECORDFOR~~~~............................................... CONFERENCEOF CONNECTICUTENTOMOLOGISTS ........................... TNSPECTION OFNURSERIES.1939 ........................................ Number and Size of Nurseries ...................................... Connectic~~tNursery Firms Certified in 1939 ......................... Other Kincls of Certificates Issued ................................... Inspection of Imported Nursery Stock ............................... Results of Inspection .......................................... INSPECTIONOFAPIA~IES,1939 .......................................... Statistics of Inspection ............................................ I'inancialStatement ............................................... Registration of 13ces ............................................... REPORTON CONTROLOF THE GYPSYMOTH . 1938-1939 ..................... hTewEquipment.................................................. ControlOperations ................................................ Work Performed by State Men ................................. \\'ark Performed by C.C.C. R4en ................................ \\:PA Work Performed ......................................... Scouting for Brown-Tail Moth ...................................... Financialstatement .............................................. -
Understanding Earwig Phenology in Top Fruit Orchards B
Understanding earwig phenology in top fruit orchards B. Gobin 1, G. Peusens 1, R. Moerkens 2 and H. Leirs 2 Abstract Earwigs, Forficula auricularia, are key generalist predators to a variety of orchard pests. However, numbers of earwigs have declined in both organic and IPM orchards in recent years. Both Integrated and Organic fruit growers have tried to re-establish earwig populations, thus far with little success. To understand earwig population dynamics and to find measures to increase natural orchard populations, we conducted a detailed phenological survey of earwigs in orchards. Earwigs were sampled while sheltering during daytime in artificial refuges. They move into the trees from the third nymph stage onwards. In most orchards, a small second brood is produced in summer, and this has a positive impact on population size in fall. We see only minor differences in phenology between apple and pear orchards, mainly caused by differences in alternative hiding places. Earwigs show an inexplicable reduction in numbers at the timing of moulting into adults. When earwig phenology is correlated with pest phenology in apple and pear, its use for pest control of major pests is clear. Keywords: Forficula auricularia , biological control, population dynamics, apple, pear Introduction The common earwig, Forficula auricularia, is a generalist feeder that survives on plant material, mosses or fungi, but, given the chance, preferentially consumes small arthropods (Phillips 1981). A number of lab studies focussing on specific orchard pests demonstrated earwig pest consumption ability of scale insects (Karsemeijer, 1973; McLeod & Chant, 1952), aphids, (Buxton & Madge, 1976; Noppert et al., 1987; Phillips, 1981), spider mites (Phillips 1981), and Psyllids (Lenfant, et al. -
Habitat Requirements, Translocation and Management of the Critically Endangered Cromwell Chafer Beetle Prodontria Lewisii Broun
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. Habitat requirements, translocation and management of the critically endangered Cromwell chafer beetle Prodontria lewisii Broun A thesis submitted in partial fulfilment of the requirements for the degree of Masters of Science in Zoology Massey University, Palmerston North New Zealand Emma Rachel Curtin 2012 1 Abstract Translocation is an important tool for the conservation of endangered species with threatened habitats and low population numbers. Without high habitat quality, translocations have low chances of success, regardless of how many organisms are released or how well they are prepared for the release. It is therefore crucial to be able to identify sites in which translocations are most likely to be successful based on key environmental characteristics specific to the species and habitat in question. Species information is also needed to determine critical life history traits and minimum habitat fragment sizes. The Cromwell chafer beetle Prodontria lewisii Broun is an ideal candidate for translocation because it has a very limited habitat range, being entirely confined to the 81 ha Cromwell Chafer Beetle Nature Reserve (CCBNR) in Cromwell, Central Otago. The entire population is estimated to contain about 3,000 individuals. This study aimed to identify key plant and soil sites for optimum larval and adult survival by using a combination of field and laboratory-based studies. Larvae survived significantly better on the cushion plant Raoulia and on the grass Festuca rubra than on silver tussock Poa cita, despite this being the plant with which they are traditionally associated. -
The Entomologist's Record and Journal of Variation
>ss> HARVARD UNIVERSITY Library of the Museum of Comparative Zoology MCZ LIBRARY MAR 2 9 1990 ' JARVARD IVERSITY Entomologist's Record AND JOURNAL OF VARIATION EDITED BY P. A. SOKOLOFF, f.r.e.s. Vol. 101 1989 Ill CONTENTS Aberration of Gymnoscelis rufifasciata Bivoltinism in Eupithecia tripunctaria H.- (Haworth) (Lep.: Geometridae) — the S. (Lep.: Geometridae) in south-east Double-striped pug. C. W. Plant, 105. England. B.K. West, 57 Abraxas grossulariata L. (Lep.: Geo- Book talk W.J.M. Chalmers-Hunt, 275 metridae), has it been shifting its Hfe Brachypalpus laphriformis (Fallen) (Dipt.: cyclQl A. A. Allen, 13% Syrphidae) A^.L. Birkett, 59 Acleris abietana (Hiibn) (Lep.: Tortrici- Breeding Gnorimus nobilis Linn. (Col.: dae) in Aberdeenshire. M.C. Townsend, Scarabidae) in captivity. J. A. Owen. 19 208 Brimstone moth {Opisthograptis luteolata Acleris abietana (Hiibn. (Lep.: Tortrici- L.). (Lep.: Geometridae) B.K. West, 167 dae) - records and foodplants, M.R. Browne versus Watson: Round two. R.R. Young. 37 Uhthoff-Kaufmann, 61. Agonopterix carduella Hiibner (Lep.: Bryaxis puncticollis Denny (Col.: Psela- Oecophoridae) in October. J.M. Chal- phidae) apparently new to Kent. A. A. mers-Hunt, 39 Allen, 11 Agriopis marginaria Fab. (Lep.: Geometri- Butterflies in winter. A. Archer-Lock, 117 dae), the Dotted-border moth caught in Butterflies of New Providence Island, December, A.M. Riley. 35 Bahamas, A further review. B.K. West, Agrotis ipsilon Hufn. (Lep.: Noctuidae) 109 Butterfly in March. J. Owen, 187 records from Dorset, 1988. A.M. and D.K. Riley, 33 An apparently new species of Homoneura (Dipt.: Lauxaniidae) from north-west Cacoecimorpha pronubana (Hiibn.) (Lep.: Kent. -
Woolly Apple Aphid Eriosoma Lanigerum Hausmann Ecology and Its Relationship with Climatic Variables and Natural Enemies in Mediterranean Areas
Bulletin of Entomological Research (2015) 105,60–69 doi:10.1017/S0007485314000753 © Cambridge University Press 2014. This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/ licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. Woolly apple aphid Eriosoma lanigerum Hausmann ecology and its relationship with climatic variables and natural enemies in Mediterranean areas Jaume Lordan*, Simó Alegre, Ferran Gatius, M. José Sarasúa and Georgina Alins IRTA – Fruitcentre, Parc Científic i Tecnològic Agroalimentari de Lleida. Parc de Gardeny, edifici Fruitcentre, 25003 Lleida, Spain Abstract A multilateral approach that includes both biotic and climatic data was developed to detect the main variables that affect the ecology and population dynamics of woolly apple aphid Eriosoma lanigerum (Hausmann). Crawlers migrated up and down the trunk mainly from spring to autumn and horizontal migration through the canopy was observed from May to August. Winter temperatures did not kill the canopy colonies, and both canopy and root colonies are the source of reinfestations in Mediterranean areas. Thus, control measures should simultaneously address roots and canopy. European earwigs Forficula auricularia (Linnaeus) were found to reduce the survival of overwintering canopy colonies up to June, and this can allow their later control by the parasitoid Aphelinus mali (Haldeman) from summer to fall. Preliminary models to predict canopy infestations were developed. Keywords: Aphelinus mali, crawler, European earwig, Forficula auricularia, multivariate analysis, winter survival (Accepted 2 September 2014; First published online 22 October 2014) Introduction (Asante et al., 1993; Asante, 1994, 1999) and South Africa (Pringle & Heunis, 2001, 2008; Heunis & Pringle, 2006; Woolly apple aphid (WAA), Eriosoma lanigerum Damavandian & Pringle, 2007;). -
Comparison of Invertebrates and Lichens Between Young and Ancient
Comparison of invertebrates and lichens between young and ancient yew trees Bachelor agro & biotechnology Specialization Green management 3th Internship report / bachelor dissertation Student: Clerckx Jonathan Academic year: 2014-2015 Tutor: Ms. Joos Isabelle Mentor: Ms. Birch Katherine Natural England: Kingley Vale NNR Downs Road PO18 9BN Chichester www.naturalengland.org.uk Comparison of invertebrates and lichens between young and ancient yew trees. Natural England: Kingley Vale NNR Foreword My dissertation project and internship took place in an ancient yew woodland reserve called Kingley Vale National Nature Reserve. Kingley Vale NNR is managed by Natural England. My dissertation deals with the biodiversity in these woodlands. During my stay in England I learned many things about the different aspects of nature conservation in England. First of all I want to thank Katherine Birch (manager of Kingley Vale NNR) for giving guidance through my dissertation project and for creating lots of interesting days during my internship. I want to thank my tutor Isabelle Joos for suggesting Kingley Vale NNR and guiding me during the year. I thank my uncle Guido Bonamie for lending me his microscope and invertebrate books and for helping me with some identifications of invertebrates. I thank Lies Vandercoilden for eliminating my spelling and grammar faults. Thanks to all the people helping with identifications of invertebrates: Guido Bonamie, Jon Webb, Matthew Shepherd, Bryan Goethals. And thanks to the people that reacted on my posts on the Facebook page: Lichens connecting people! I want to thank Catherine Slade and her husband Nigel for being the perfect hosts of my accommodation in England. -
Conserving Species-Rich Predator Assemblages Strengthens Natural Pest Control in a Climate Warming Context
Agricultural and Forest Entomology (2016), DOI: 10.1111/afe.12180 Conserving species-rich predator assemblages strengthens natural pest control in a climate warming context ∗†‡ ∗† Robin Drieu and Adrien Rusch ∗INRA, ISVV, UMR 1065 Santé et Agroécologie du Vignoble, F-33883, 71 rue Edouard Bourlaux, Villenave d’Ornon, France, †INRA UMR 1065 Santé et Agroécologie du Vignoble, Bordeaux Sciences Agro, Université de Bordeaux, F-33883, 71 rue Edouard Bourlaux, Villenave d’Ornon, France and ‡Centre International D’études Supérieures en Sciences Agronomiques, Montpellier SupAgro, Place Pierre Viala, 34060, Montpellier, France Abstract 1 Recent evidence has shown that a consideration of multiple drivers is important if we want to understand how ecosystem functioning will respond to global change. 2 In the present study, we used a substitutive approach to examine how two major components of global change, warming and predator diversity, affect the top-down control of two phytophagous insect pests. Predator assemblages were created using a substitutive design to give three single-species treatments (low diversity) and one three-species treatment (high diversity) under two temperature treatments (current seasonal temperature and an increase of +3∘C over current temperatures). 3 The results obtained indicate a shift from substitutive to complementarity effects among predatory species with experimental warming. Experimental warming revealed complementarity between the predatory species in diverse assemblages because higher predation rates on both prey species were found in the high diversity treatment compared with what was expected based on low diversity treatments at the same temperature. 4 Our analyses of prey selectivity provided evidence that resource-niche partitioning is involved in the emergence of functional complementarity under warming.