A Guide to the Shropshire Orthoptera and Dermaptera by David W. Williams
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Entomology Day 2018 Wyre Forest Study Group
Wyre Forest Study Group Entomology Day 2018 ChaIR: Brett WestwOOD, RepOrt: SUsan LIMbreY Flights of Fancy Speakers from left: Wendy Carter, Steven Falk, Richard Comont, Brett Westwood, Malcolm Smart, Erica McAlister, Gary Farmer Steve Horton Chaired by Brett Westwood, our title gave speak- in 1983, this book, with its simple keys, big genera di- ers scope to cover a range of topics, out of which a vided into smaller keys and short snappy text with an recurring theme of concern about pollinating insects ecological flavour, made recording much easier, broke became apparent. down barriers, and influenced Steven’s own later work. He spent his second undergraduate year doing 13 dip- Steven Falk, in Breaking Down Barriers to In- tera plates for Michael Chinery’s Collins Guide to the vertebrate Identification, told us that throughout Insects of Britain and Northern Europe (1986), one of his career he has been committed to making entomol- five artists illustrating 2000 species, another ground- ogy accessible no matter what level of expertise peo- breaking book. Steven showed us how his technique ple may have. He started as an artist, and he showed us progressed through the book, for example with lateral some of his childhood, but far from childish, pictures of lighting giving a three dimensional effect. birds. He was as fascinated by the literature and by the artists and their techniques, as by the natural history, In 1985, work began on illustrations for George Else’s citing Roger Tory Peterson, the father of modern user- Handbook to British Bees. Pen and ink, using combi- friendly field guides, the draughtsmanship of Charles nations of stippling and cross-hatching, produced an Tunnicliffe using watercolours, and Basil Ede, using amazing array of tones and textures, and Steven ac- gouache, among others. -
A Review of the Japanese Kateretidae Fauna (Coleoptera: Cucujoidea)
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Published 9.xii.2011 Volume 51(2), pp. 551–585 ISSN 0374-1036 A review of the Japanese Kateretidae fauna (Coleoptera: Cucujoidea) Sadatomo HISAMATSU Entomological Laboratory, Faculty of Agriculture, Ehime University, Tarumi 3–5–7, Matsuyama, 790–8566 Japan; e–mail: [email protected] Abstract. The family Kateretidae of Japan is revised. Nine species belonging to 6 genera are recognized, including: Kateretes japonicus Hisamatsu, 1985, K. takagii S-T. Hisamatsu, 2006, Platamartus jakowlewi Reitter, 1892, Heterhelus (Heterhelus) scutellaris (Heer, 1841), H. (Heterhelus) morio (Reitter, 1878), H. (Boreades) solani (Heer, 1841), Sibirhelus corpulentus (Reitter, 1900), Brachyp- terus urticae (Fabricius, 1792), and Brachypterolus pulicarius (Linnaeus, 1758). Heterhelus morio, which was synonymized under H. scutellaris by KIREJTSHUK (1989), is found to be a valid species, and is herein resurrected. Platamartus jakowlewi is newly recorded from Japan. Brachypterolus shimoyamai Hisamatsu, 1985, syn. nov., is synonymized under Brachypterolus pulicarius. Dorsal habitus images, illustrations of male and female genitalia, and other important diagnostic characters are provided for all species. A key for identifi cation of all Japanese taxa is also provided. Key words. Coleoptera, Kateretidae, taxonomy, new synonym, new record, key, Japan, Palaearctic Region Introduction The family Kateretidae, belonging to the superfamily Cucujoidea, is mainly distributed in the Holarctic Region, and comprises about 95 species within 14 genera worldwide (JELÍNEK & CLINE 2010). Both larval and adult Kateretidae are anthophagous: the larvae are monophagous or oligophagous, while adults are more generalized feeders, occurring on true host plants only during mating and ovipositing periods; otherwise, they feed on a broader assortment of fl owering plants (JELÍNEK & CLINE 2010). -
Invasion of the Body Snatchers: the Diversity and Evolution of Manipulative Strategies in Host–Parasite Interactions
CHAPTER 3 Invasion of the Body Snatchers: The Diversity and Evolution of Manipulative Strategies in Host–Parasite Interactions † Thierry Lefe`vre,* Shelley A. Adamo, ‡ David G. Biron, Dorothe´e Misse´,* § k } David Hughes, , ,1 and Fre´de´ric Thomas*, ,1 Contents 3.1. Introduction 46 3.2. How Parasites Alter Host Behaviour 49 3.2.1. Parasitic effects on host neural function 49 3.2.2. Proteomics and proximate mechanisms 56 3.3. A Co-Evolutionary Perspective 66 3.3.1. Exploiting host-compensatory responses 66 3.2.2. Facultative virulence 72 3.4. The (River) Blind Watchmaker 75 3.5. Concluding Remarks 76 References 76 Abstract Parasite-induced alteration of host behaviour is a widespread trans- mission strategy among pathogens. Understanding how it works is an exciting challenge from both a mechanistic and an evolutionary perspective. In this review, we use key examples to examine the * Ge´ne´tique et Evolution des Maladies Infectieuses, UMR CNRS/IRD 2724, Montpellier, France { Department of Psychology, Dalhousie University, Halifax, Canada { PIAF, UMR 547 INRA/Universite´ Blaise-Pascal, Clermont-Ferrand, France § Department of Organismal Biology, University of Harvard, Cambridge, MA, USA } Institut de recherche en biologie ve´ge´tale, De´partement de sciences biologiques Universite´ de Montre´al, Montre´al, Que´bec, Canada k School of Biosciences, University of Exeter, Exeter, UK 1 Both authors contributed equally Advances in Parasitology, Volume 68 # 2009 Elsevier Ltd. ISSN 0065-308X, DOI: 10.1016/S0065-308X(08)00603-9 All rights reserved. 45 46 Thierry Lefe`vre et al. proximate mechanisms by which parasites are known to control the behaviour of their hosts. -
ED45E Rare and Scarce Species Hierarchy.Pdf
104 Species 55 Mollusc 8 Mollusc 334 Species 181 Mollusc 28 Mollusc 44 Species 23 Vascular Plant 14 Flowering Plant 45 Species 23 Vascular Plant 14 Flowering Plant 269 Species 149 Vascular Plant 84 Flowering Plant 13 Species 7 Mollusc 1 Mollusc 42 Species 21 Mollusc 2 Mollusc 43 Species 22 Mollusc 3 Mollusc 59 Species 30 Mollusc 4 Mollusc 59 Species 31 Mollusc 5 Mollusc 68 Species 36 Mollusc 6 Mollusc 81 Species 43 Mollusc 7 Mollusc 105 Species 56 Mollusc 9 Mollusc 117 Species 63 Mollusc 10 Mollusc 118 Species 64 Mollusc 11 Mollusc 119 Species 65 Mollusc 12 Mollusc 124 Species 68 Mollusc 13 Mollusc 125 Species 69 Mollusc 14 Mollusc 145 Species 81 Mollusc 15 Mollusc 150 Species 84 Mollusc 16 Mollusc 151 Species 85 Mollusc 17 Mollusc 152 Species 86 Mollusc 18 Mollusc 158 Species 90 Mollusc 19 Mollusc 184 Species 105 Mollusc 20 Mollusc 185 Species 106 Mollusc 21 Mollusc 186 Species 107 Mollusc 22 Mollusc 191 Species 110 Mollusc 23 Mollusc 245 Species 136 Mollusc 24 Mollusc 267 Species 148 Mollusc 25 Mollusc 270 Species 150 Mollusc 26 Mollusc 333 Species 180 Mollusc 27 Mollusc 347 Species 189 Mollusc 29 Mollusc 349 Species 191 Mollusc 30 Mollusc 365 Species 196 Mollusc 31 Mollusc 376 Species 203 Mollusc 32 Mollusc 377 Species 204 Mollusc 33 Mollusc 378 Species 205 Mollusc 34 Mollusc 379 Species 206 Mollusc 35 Mollusc 404 Species 221 Mollusc 36 Mollusc 414 Species 228 Mollusc 37 Mollusc 415 Species 229 Mollusc 38 Mollusc 416 Species 230 Mollusc 39 Mollusc 417 Species 231 Mollusc 40 Mollusc 418 Species 232 Mollusc 41 Mollusc 419 Species 233 -
Of Agrocenosis of Rice Fields in Kyzylorda Oblast, South Kazakhstan
Acta Biologica Sibirica 6: 229–247 (2020) doi: 10.3897/abs.6.e54139 https://abs.pensoft.net RESEARCH ARTICLE Orthopteroid insects (Mantodea, Blattodea, Dermaptera, Phasmoptera, Orthoptera) of agrocenosis of rice fields in Kyzylorda oblast, South Kazakhstan Izbasar I. Temreshev1, Arman M. Makezhanov1 1 LLP «Educational Research Scientific and Production Center "Bayserke-Agro"», Almaty oblast, Pan- filov district, Arkabay village, Otegen Batyr street, 3, Kazakhstan Corresponding author: Izbasar I. Temreshev ([email protected]) Academic editor: R. Yakovlev | Received 10 March 2020 | Accepted 12 April 2020 | Published 16 September 2020 http://zoobank.org/EF2D6677-74E1-4297-9A18-81336E53FFD6 Citation: Temreshev II, Makezhanov AM (2020) Orthopteroid insects (Mantodea, Blattodea, Dermaptera, Phasmoptera, Orthoptera) of agrocenosis of rice fields in Kyzylorda oblast, South Kazakhstan. Acta Biologica Sibirica 6: 229–247. https://doi.org/10.3897/abs.6.e54139 Abstract An annotated list of Orthopteroidea of rise paddy fields in Kyzylorda oblast in South Kazakhstan is given. A total of 60 species of orthopteroid insects were identified, belonging to 58 genera from 17 families and 5 orders. Mantids are represented by 3 families, 6 genera and 6 species; cockroaches – by 2 families, 2 genera and 2 species; earwigs – by 3 families, 3 genera and 3 species; sticks insects – by 1 family, 1 genus and 1 species. Orthopterans are most numerous (8 families, 46 genera and 48 species). Of these, three species, Bolivaria brachyptera, Hierodula tenuidentata and Ceraeocercus fuscipennis, are listed in the Red Book of the Republic of Kazakhstan. Celes variabilis and Chrysochraon dispar indicated for the first time for a given location. The fauna of orthopteroid insects in the studied areas of Kyzylorda is compared with other regions of Kazakhstan. -
Generation of Extreme Ultrasonics in Rainforest Katydids Fernando Montealegre-Z1,*, Glenn K
4923 The Journal of Experimental Biology 209, 4923-4937 Published by The Company of Biologists 2006 doi:10.1242/jeb.02608 Generation of extreme ultrasonics in rainforest katydids Fernando Montealegre-Z1,*, Glenn K. Morris2 and Andrew C. Mason1 1Integrative Behaviour and Neuroscience Group, Department of Life Sciences, University of Toronto at Scarborough, 1265 Military Trail, Scarborough, Ontario, Canada, M1C 1A4 and 2Department of Biology, University of Toronto at Mississauga, 3359 Mississauga Road, Mississauga, Ontario, Canada, L5L 1C6 *Author for correspondence: (e-mail: [email protected]) Accepted 19 October 2006 Summary The calling song of an undescribed Meconematinae species make pure-tone ultrasonic pulses. Wing velocities katydid (Tettigoniidae) from South America consists of and carriers among these pure-tone species fall into two trains of short, separated pure-tone sound pulses at groups: (1) species with ultrasonic carriers below 40·kHz 129·kHz (the highest calling note produced by an that have higher calling frequencies correlated with higher Arthropod). Paradoxically, these extremely high- wing-closing velocities and higher tooth densities: for these frequency sound waves are produced by a low-velocity katydids the relationship between average tooth strike movement of the stridulatory forewings. Sound production rate and song frequency approaches 1:1, as in cricket during a wing stroke is pulsed, but the wings do not pause escapement mechanisms; (2) a group of species with in their closing, requiring that the scraper, in its travel ultrasonic carriers above 40·kHz (that includes the along the file, must do so to create the pulses. We Meconematinae): for these katydids closing wing velocities hypothesize that during scraper pauses, the cuticle behind are dramatically lower and they make short trains of the scraper is bent by the ongoing relative displacement of pulses, with intervening periods of silence greater than the the wings, storing deformation energy. -
Nimfal Conocephalus Fuscus Fuscus (Fabricius, 1793) (Orthoptera, Tettigoniidae)’Ta Proventrikulusun Histomorfolojik Özellikleri
ISSN 2757-5543 GÜFFD 2. Cilt (1): 68-76 (2021) DOI: 10.5281/zenodo.4843474 Gazi Üniversitesi Fen Fakültesi Dergisi http://sci-fac-j.gazi.edu.tr/ Nimfal Conocephalus fuscus fuscus (Fabricius, 1793) (Orthoptera, Tettigoniidae)’ta Proventrikulusun Histomorfolojik Özellikleri Damla Amutkan Mutlu1,* , Irmak Polat2 , Zekiye Suludere2 1 Gazi Üniversitesi, Fen Fakültesi, Biyoloji Bölümü, 06500, Ankara, Türkiye 2 Çankırı Karatekin Üniversitesi, Fen Fakültesi, Biyoloji Bölümü, 18200, Çankırı, Türkiye Öne Çıkanlar • Nimfal Conocephalus fuscus fuscus’ta proventrikulusun morfolojik ve yapısal özellikleri incelenmiştir. • Çalışmada ışık mikroskobu ve taramalı elektron mikroskop yöntemleri kullanılmıştır. • Diğer böcek türlerinin proventrikulusu ile benzerlikleri ve farklılıkları ortaya konmuştur. Makale Bilgileri Özet Böceklerde sindirim sisteminin morfolojisindeki çeşitlilik, birçok araştırmacıyı, proventrikulusa özel vurgu Geliş: 29.03.2021 yaparak, onu sistematik ve filogenik karakter olarak kullanmaya yöneltmiştir. Bu çalışmada, nimfal Kabul: 06.05.2021 Conocephalus fuscus fuscus (Fabricius, 1793) (Orthoptera, Tettigoniidae), 2017 ve 2018 yıllarının Haziran ayında Ankara-Çankırı yolu üzerindeki arazilerden toplanmış ve disekte edilen proventrikulus yapısı ışık mikroskobu ve taramalı elektron mikroskop yöntemleriyle incelenmiştir. C. fuscus fuscus dıştan içe doğru Anahtar Kelimeler kas tabakası ve epitel tabakasından oluşmaktadır. Epitel tabakasının apikal yüzeyinde farklı kalınlıklarda kütikül tabakası yer almaktadır. C. fuscus fuscus, 6 skletorize -
Orthoptera, Acrididae) at Non-Outbreaking and Outbreaking Situations
SHORT COMMUNICATION Longevity and fecundity of Dichroplus maculipennis (Orthoptera, Acrididae) at non-outbreaking and outbreaking situations Yanina Mariottini1, María Laura De Wysiecki1 & Carlos Ernesto Lange1,2 1Centro de Estudios Parasitológicos y de Vectores (UNLP- CCT La Plata- CONICET). Calle 2 Nº 584, Código postal 1900, La Plata, Argentina. [email protected], [email protected] 2Comisión de Investigaciones Científicas provincia de Buenos Aires. [email protected] ABSTRACT. Longevity and fecundity of Dichroplus maculipennis (Orthoptera, Acrididae) at non-outbreaking and outbreaking situations. Dichroplus maculipennis is one of the most characteristic and damaging grasshopper species of Argentina, mainly in areas of the Pampas and Patagonia regions. We estimated and compared the longevity and fecundity of adult female D. maculipennis under controlled conditions (30°C, 14L:10D, 40% RH) from individuals collected as last instar nymphs (VI) in the field and with a known recent history of low and high density conditions. Densities of D. maculipennis at the collecting sites were 0.95 individuals per m2 in 2006 and 46 ind/m2 in 2009, representing non-outbreaking and outbreaking situations, respectively. Adult female longev- ity in 2006 (67.96 ± 3.2 days) was significantly higher (p < 0.05) than in 2009 (37.44 ± 1.98 days). The number of egg-pods per female was 3.32 ± 0.44 for 2006 and 1.62 ± 0.26 for 2009. The average fecundity in 2006 (89.29 ± 11.9 eggs/female) was signifi- cantly greater (p < 0.05) than that in 2009 (36.27 ± 5.82 eggs/female). While it was observed that the oviposition rate was higher in 2006, this difference was not significant (p > 0.05). -
Metabarcoding for the Parallel Identification of Several Hundred Predators And
bioRxiv preprint doi: https://doi.org/10.1101/155721; this version posted June 26, 2017. 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. Metabarcoding for the parallel identification of several hundred predators and their preys: application to bat species diet analysis MAXIME GALAN*1, JEAN-BAPTISTE PONS2, ORIANNE TOURNAYRE1, ERIC PIERRE1, MAXIME LEUCHTMANN3, DOMINIQUE PONTIER2.4.* and NATHALIE CHARBONNEL1* Full postal addresses 1CBGP, INRA, CIRAD, IRD, MontpElliEr SupAgro, Univ. MontpelliEr, MontpelliEr, FrancE 2Univ Lyon, LabEx ECOFECT EcoEvolutionary Dynamics of InfEctious DisEasEs, Villeurbanne F-69365 Lyon, France 3 Nature EnvironnEment, 2 AvEnuE Saint-Pierre, 17700 Surgères, France 4Univ Lyon, UnivErsité Lyon 1, CNRS, LaboratoirE dE BiométriE Et BiologiE ÉvolutivE UMR5558, F-69622 Villeurbanne, France * equal author contributions Keywords (4-6): Chiroptera, arthropods, Environmental DNA (EDNA), high-throughput sequencing, false positives, predator–prey interactions Name, address, fax number and email of corresponding author * Maxime Galan, INRA, UMR CBGP (INRA/IRD/CIRAD/MontpElliEr Supagro/Univ. MontpelliEr), 755 avEnue du Campus Agropolis, CS 300 16, F-34988 Montferrier-sur-Lez cedex, France. Fax: (+00 33) 04 99 62 33 05; E-mail: [email protected] Running title : Metabarcoding of prEdators and their preys 1 bioRxiv preprint doi: https://doi.org/10.1101/155721; this version posted June 26, 2017. 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. -
Eupholidoptera Garganica (Orthoptera: Tettigoniidae) in Budapest, Hungary
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/331893795 Eupholidoptera garganica (Orthoptera: Tettigoniidae) in Budapest, Hungary Article in Acta Phytopathologica et Entomologica Hungarica · December 2018 DOI: 10.17112/FoliaEntHung.2018.79.37 CITATIONS READS 0 102 1 author: Gellért Puskás Hungarian Natural History Museum 29 PUBLICATIONS 101 CITATIONS SEE PROFILE Some of the authors of this publication are also working on these related projects: Orthoptera fauna of the Hungarian Middle Mountain View project Local and Global Factors in Organization of Central-European Orthopteran Assemblages View project All content following this page was uploaded by Gellért Puskás on 20 March 2019. The user has requested enhancement of the downloaded file. FOLIA ENTOMOLOGICA HUNGARICA ROVARTANI KÖZLEMÉNYEK Volume 79 2018 pp. 37–43 Eupholidoptera garganica (Orthoptera: Tettigoniidae) in Budapest, Hungary Gellért Puskás Hungarian Natural History Museum, Department of Zoology, H-1088 Budapest, Baross u. 13, Hungary. E-mail: [email protected] Abstract – A small introduced population of Eupholidoptera garganica La Greca, 1959 (Orthop- tera: Tettigoniidae: Tettigoniinae: Pholidopterini) was found in a garden suburb of Albertfalva, part of Budapest. Altogether 8 singing males were detected in July 2018, on a less than 2 hectare area. Th e origin of the population is unknown; the species arrived most probably accidentally with horticultural plants from Italy. With 4 fi gures. Key words – established population, faunistics, introduced species, urban environment INTRODUCTION Th e anthropogenic spread of insects is a world-wide phenomenon (e.g. Kenis et al. 2009). In Hungary 170 invertebrates are regarded as invasive spe- cies (Báldi et al. -
13 CHAPTER 2 LITERATURE REVIEW 2.1 Biology of Tree Species
13 CHAPTER 2 LITERATURE REVIEW 2.1 Biology of tree species in interaction with their insect pests The description of the tree species examined in this thesis is meant to provide a general background of the biology, growing conditions, properties and uses of those species, describing the interactions and stages of the considered insect pest. Each of the species are well known and widely distributed urban tree species which enhances their pest problems to a larger scale of consideration. 2.1.1 Oak tree with Oak processionary moth The Oak trees considered are of the species Quercus robur L., which are native to most of Europe, Anatolia, Caucasus and parts of North Africa. Q. robur is a large deciduous tree reaching heights of 25–35 m in average and circumferences exceeding other tree species reaching four meters to exceptional twelve meters. The species is known for its hard and durable timber and counts as one of the most common and important deciduous forest species with attributes for many desired uses. Construction, furniture, toys, firewood with high calorific value and even for the barrels of the “Barrique wine”, a special treat, this high quality timber is expedient. The hard and durable wood allows the trees to reach ages up to around 1000 years, even in Europe’s temperate and humid climate. 14 The leaves are lobed, nearly sessile and very distinct. Q. robur is also valued for its importance to insects and other wildlife. Numerous insects live on the leaves, the fine bark of the twigs, the nutritious buds and fruits, which are called acorns and shown in Figure 2.1a-c. -
The Evolution of Complex Calls in Meadow
THE EVOLUTION OF COMPLEX CALLS IN MEADOW KATYDIDS _______________________________________ A Dissertation presented to the Faculty of the Graduate School at the University of Missouri-Columbia _______________________________________________________ In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy _____________________________________________________ by NATHAN HARNESS Dr. Johannes Schul, Dissertation Supervisor July 2018 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled THE EVOLUTION OF COMPLEX CALLS IN MEADOW KATYDIDS presented by Nathan Harness, a candidate for the degree of doctor of philosophy, and hereby certify that, in their opinion, it is worthy of acceptance. Professor Johannes Schul Professor Sarah Bush Professor Lori Eggert Professor Patricia Friedrichsen For my family Rachel and Mayr have given me so much. They show me unselfish affection, endless support, and generosity that seems to only grow. Without them the work here, and the adventure we’ve all three gone on surrounding it, would not have been possible. They have sacrificed birthdays, anniversaries, holidays, and countless weekends and evenings. They’ve happily seen me off to weeks of field work and conference visits. I am thankful to them for being so generous, and completely lacking in resentment at all the things that pull their husband and dad in so many directions. They have both necessarily become adept at melting away anxiety; I will forever be indebted to the hugs of a two-year-old and the kind words of his mom. Rachel and Mayr both deserve far more recognition than is possible here. I also want to thank my parents and brother and sisters.