The Entomological Diversity of Pokémon
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Molecular Insights Into the Phylogenetic Structure of the Spider
MolecularBlackwell Publishing Ltd insights into the phylogenetic structure of the spider genus Theridion (Araneae, Theridiidae) and the origin of the Hawaiian Theridion-like fauna MIQUEL A. ARNEDO, INGI AGNARSSON & ROSEMARY G. GILLESPIE Accepted: 9 March 2007 Arnedo, M. A., Agnarsson, I. & Gillespie, R. G. (2007). Molecular insights into the phylo- doi:10.1111/j.1463-6409.2007.00280.x genetic structure of the spider genus Theridion (Araneae, Theridiidae) and the origin of the Hawaiian Theridion-like fauna. — Zoologica Scripta, 36, 337–352. The Hawaiian happy face spider (Theridion grallator Simon, 1900), named for a remarkable abdominal colour pattern resembling a smiling face, has served as a model organism for under- standing the generation of genetic diversity. Theridion grallator is one of 11 endemic Hawaiian species of the genus reported to date. Asserting the origin of island endemics informs on the evolutionary context of diversification, and how diversity has arisen on the islands. Studies on the genus Theridion in Hawaii, as elsewhere, have long been hampered by its large size (> 600 species) and poor definition. Here we report results of phylogenetic analyses based on DNA sequences of five genes conducted on five diverse species of Hawaiian Theridion, along with the most intensive sampling of Theridiinae analysed to date. Results indicate that the Hawai- ian Islands were colonised by two independent Theridiinae lineages, one of which originated in the Americas. Both lineages have undergone local diversification in the archipelago and have convergently evolved similar bizarre morphs. Our findings confirm para- or polyphyletic status of the largest Theridiinae genera: Theridion, Achaearanea and Chrysso. -
The Reading Naturalist
The Reading Naturalist No. 53 Published by the Reading and District Natural History Society 2001 Price to Non Members £2.50 T H E R E A D I N G N A T U R A L I S T No 53 for the year 2000 The Journal of the Reading and District Natural History Society President Mr Rod d’Ayala Honorary General Secretary Mrs Catherine Butcher Honorary Editor Dr Malcolm Storey Editorial Sub-committee The Editor, Dr Alan Brickstock, Mrs Linda Carter, Mr Hugh H. Carter Miss June M. V. Housden, Mr David G. Notton Honorary Recorders Botany: Mrs Linda Carter, Fungi: Dr Alan Brickstock Entomology: Mr David G. Notton Invertebates other than insects: Mr Hugh H. Carter Vertebrates: Mr Hugh H. Carter CONTENTS Obituary 1 Members’ Observations 1 Excursions Meryl Beek 2 Wednesday Afternoon Walks Alan Brickstock 5 Meetings (1999-2000) Catherine Butcher 6 The Fishlock Prize 7 Membership Norman Hall 8 Presidential address: Some Mycological Ramblings Alan Brickstock 9 Natural History Services provided at the Museum of Reading David G. Notton 13 A Mutant Foxglove Malcolm Storey 16 Sehirus dubius (or should that be dubious!) Chris Raper 17 Hartslock – a Local Success Story Chris Raper 17 Recorders’ Reports Malcolm Storey 19 “RDB” and “N” status – The Jargon Explained Rod d’Ayala 19 Recorder’s Report for Botany 2000 Linda Carter 20 The New Berkshire Flora Malcolm Storey 23 Recorder’s Report for Mycology 2000 Alan Brickstock 24 Recorder’s Report for Entomology 2000 David G. Notton 27 Recorder’s Report for Invertebrates other than insects 2000 Hugh H. -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
A Contribution to the Knowledge of the Tenthredinidae (Symphyta, Hymenoptera)
TurkJZool 28(2004)37-54 ©TÜB‹TAK AContributiontotheKnowledgeoftheTenthredinidae (Symphyta,Hymenoptera)FaunaofTurkey PartI:TheSubfamilyTenthredininae* ÖnderÇALMAfiUR,HikmetÖZBEK AtatürkUniversity,FacultyofAgriculture,DepartmentofPlantProtection, 25240Erzurum-TURKEY Received:07.02.2003 Abstract: ThesubfamilyTenthredininaeinthefamilyTenthredinidaewastreatedinthispartofthestudyregardingthesawfly (Symphyta,Hymenoptera)faunaofTurkey.Thematerialswerecollectedfromvariouslocalitiesaroundthecountry,though examplesfromeasternTurkeyarepredominant.Afterexaminingmorethan2500specimens,57speciesin8generawererecorded. ElevenspecieswerenewforTurkishfauna;ofthese3specieswererecordedforthefirsttimeasAsianfauna.Furthermore,3 specieswereendemicforTurkey.ThedistributionandnewareasaswellasthehostplantsofsomespeciesaroundTurkeyandth e worldweregiven.Foreachspeciesitschorotypewasreported. KeyWords: Hymenoptera,Tenthredinidae,Tenthredininae,Fauna,Turkey Türkiye’ninTenthredinidae(Symphyta,Hymenoptera)Faunas›naKatk›lar Bölüm:ITenthredininaeAltfamilyas› Özet: Türkiye’nintestereliar›(Symphyta,Hymenoptera)faunas›n›ntespitineyönelikçal›flmalar›nbubölümünde;Tenthredininae (Tenthredinidae)altfamilyas›eleal›nm›fl;incelenen2500’denfazlaörneksonucu,sekizcinseba¤l›toplam57türsaptanm›flt›r. Türkiyefaunas›içinyeniolduklar›saptanan11türdenüçününAsyafaunas›içindeyenikay›tolduklar›belirlenmifltir.ÜçtürünTürkiye içinendemikolduklar›saptanm›flt›r.Tespitedilentürlerinhementamam›içinyeniyay›lmaalanlar›belirlenmifl,birço¤unun konukçular›bulunmufltur.Türkiyevedünyadakida¤›l›fllar›chorotype’leriilebirlikteverilmifltir. -
Taxonomic Review of Drilini (Elateridae: Agrypninae) in Cameroon Reveals High Morphological Diversity, Including the Discovery of Five New Genera
Insect Systematics & Evolution 48 (2017) 441–492 brill.com/ise Taxonomic review of Drilini (Elateridae: Agrypninae) in Cameroon reveals high morphological diversity, including the discovery of five new genera Robin Kundrata* and Ladislav Bocak Department of Zoology, Faculty of Science, Palacky University, 17. listopadu 50, 771 46, Olomouc, Czech Republic *Corresponding author, e-mail: [email protected] Version of Record, published online 7 April 2017; published in print 1 November 2017 Abstract The first comprehensive survey of the Cameroonian Drilini fauna is presented. High diversity was identi- fied in the zone of tropical rain forest and five genera are proposed: Flabelloselasia gen. n., Kupeselasia gen. n., Lolosia gen. n., Microselasia gen. n., and Wittmerselasia gen. n. with the subgenus Latoselasia subgen. n. The following species are described: Flabelloselasia oculata sp. n., Kupeselasia minuta sp. n., Lolosia transversalis sp. n., Microselasia barombi sp. n., M. elongata sp. n., M. gracilis sp. n., M. grandis sp. n., M. kupensis sp. n., M. lolodorfensis sp. n., M. macrocephala sp. n., M. obscura sp. n., M. pseudograndis sp. n., Wittmerselasia camerooniana sp. n., W. davidsoni sp. n., W. geiseri sp. n., W. variabilis sp. n., and W. (Latoselasia) similis sp. n. Selasia maculata Wittmer, 1989 is redescribed and transferred to Wittmerselasia gen. n. as W. maculata (Wittmer, 1989), comb. n. Taxonomically important characters are illustrated for all genera and species and an identification key for Drilini from Cameroon is provided. Keywords Elateroidea; Selasia; Africa; diversity hot-spot; distribution Introduction Drilini is a small morphologically distinct beetle lineage with the soft-bodied, fully winged males and larviform apterous females (Crowson 1972; Bocak et al. -
Sambia Succinica, a Crown Group Tenthredinid from Eocene Baltic Amber (Hymenoptera: Tenthredinidae)
Insect Systematics & Evolution 43 (2012) 271–281 brill.com/ise Sambia succinica, a crown group tenthredinid from Eocene Baltic amber (Hymenoptera: Tenthredinidae) Lars Vilhelmsena,* and Michael S. Engelb aNatural History Museum of Denmark, University of Copenhagen, Universitetsparken 15, DK-2100 Copenhagen, Denmark bDivision of Entomology (Paleoentomology), Natural History Museum and Department of Ecology & Evolutionary Biology, 1501 Crestline Drive, Suite 140, University of Kansas, Lawrence KS 66045, USA *Corresponding author, e-mail: [email protected] Published 17 December 2012 Abstract Sambia succinica gen. et sp.n. from Eocene Baltic amber is described and illustrated. It is apparently the first amber fossil that can be definitively assigned to Tenthredininae. It displays two diagnostic forewing characters for this subfamily: having a bend distally in vein R and the junctions of veins M and Rs + M with vein R being some distance from each other. The variance and possible transitions between the anal vein configurations among the genera in Tenthredininae is briefly discussed. Keywords amber inclusion, sawfly, Tertiary, Eocene, taxonomy Introduction Tenthredinidae is the largest family of non-apocritan Hymenoptera by far, comprising more than 5500 described species (Huber 2009; Taeger & Blank 2010). Together with five other families they comprise the Tenthredinoidea or true sawflies. The larvae of the members of the superfamily are all herbivores and most are external feeders on green parts of angiosperms; however, other host plants and feeding modes (e.g., leafrolling, leafmining, or galling in leaves, buds and shoots; see Nyman et al. 1998, 2000) do occur. Recent comprehensive treatments of the phylogeny of the basal hymenopteran lineages, while providing strong support for the Tenthredinoidea, have consistently failed to retrieve the Tenthredinidae as monophyletic (Vilhelmsen 2001; Schulmeister 2003; Ronquist et al. -
Tarantulas and Social Spiders
Tarantulas and Social Spiders: A Tale of Sex and Silk by Jonathan Bull BSc (Hons) MSc ICL Thesis Presented to the Institute of Biology of The University of Nottingham in Partial Fulfilment of the Requirements for the Degree of Doctor of Philosophy The University of Nottingham May 2012 DEDICATION To my parents… …because they both said to dedicate it to the other… I dedicate it to both ii ACKNOWLEDGEMENTS First and foremost I would like to thank my supervisor Dr Sara Goodacre for her guidance and support. I am also hugely endebted to Dr Keith Spriggs who became my mentor in the field of RNA and without whom my understanding of the field would have been but a fraction of what it is now. Particular thanks go to Professor John Brookfield, an expert in the field of biological statistics and data retrieval. Likewise with Dr Susan Liddell for her proteomics assistance, a truly remarkable individual on par with Professor Brookfield in being able to simplify even the most complex techniques and analyses. Finally, I would really like to thank Janet Beccaloni for her time and resources at the Natural History Museum, London, permitting me access to the collections therein; ten years on and still a delight. Finally, amongst the greats, Alexander ‘Sasha’ Kondrashov… a true inspiration. I would also like to express my gratitude to those who, although may not have directly contributed, should not be forgotten due to their continued assistance and considerate nature: Dr Chris Wade (five straight hours of help was not uncommon!), Sue Buxton (direct to my bench creepy crawlies), Sheila Keeble (ventures and cleans where others dare not), Alice Young (read/checked my thesis and overcame her arachnophobia!) and all those in the Centre for Biomolecular Sciences. -
Gillespie, RG 1989. Diet-Induced Color Change in the Hawaiian Happy
Gillespie, R. G . 1989 . Diet-induced color change in the Hawaiian happy-face spider Theridion grallator (Araneae, Theridiidae) . J . Arachnol ., 17:171-177 . DIET-INDUCED COLOR CHANGE IN THE HAWAIIAN HAPPY-FACE SPIDER THERIDION GRALLATOR, (ARANEAE, THERIDIIDAE) Rosemary G. Gillespie' Department of Entomology, University of Hawaii, Honolulu, Hawaii 96822' USA ABSTRACT The Hawaiian happy-face spider Theridion grallator,Simon is a smalll spider, endemic to Hawaii, where it is found under leaves in the wet and mesic forests . The abdomen is pale, translucent yellow, but variable amounts of red, black or white pigment may be superimposed on this to generate a host of patterned morphs . The translucence of the abdomen may enhance crypsis against predators searching the underside of leaves ; the variability in the superimposed pattern may serve to counteract the development of a search image by the predator . The present study documents plasticity in base coloration, which can changee rapidly and markedly following ingestion of certain types of prey . This may be merely a consequence of abdominal translucence . But it is interesting to note that it adds a whole new dimension to the color polymorphism of the species . INTRODUCTION Color change in animals is a widespread phenomenon . It is generally associated with a change in physiological state . This in turn may be induced by ontogenetic or environmental changes, or stress . In spiders, color change is known to occur under a variety of circumstances . Ontogenetic modifictions are widespread, with the adult coloration being attained in the final molt (Bonnet 1933; Homann 1946; Millot 1949). More rapid changes in color pattern have been noted in spiders of the family Araneidae, which accumulate guanine beneath the cuticle during periods of starvation, thereby developing a pattern of opaque white blotches over the abdomen (Foelix 1979) . -
Formatting Your Paper for Submission in the Moorea Class Journal
UC Berkeley Student Research Papers, Fall 2012 Title Coloration in relation to ecology in the Asian spiny-backed spider, Thelacantha brevispina (Araneae, Araneidae) on Moorea, French Polynesia Permalink https://escholarship.org/uc/item/5524p5x6 Author Truong, Hua Publication Date 2012-12-12 Undergraduate eScholarship.org Powered by the California Digital Library University of California COLORATION IN RELATION TO ECOLOGY IN THE ASIAN SPINY-BACKED SPIDER, THELACANTHA BREVISPINA (ARANEAE, ARANEIDAE) ON MOOREA, FRENCH POLYNESIA HUA S. TRUONG Integrative Biology, University of California, Berkeley, California 94720 USA Abstract. Color polymorphism is a widespread phenomenon in many arthropods, including spiders. The persistence of these visible, readily measured polymorphisms over time suggests that they carry adaptive functions and thus are maintained by natural selection. Studying polymorphism is useful for examining evolution in action and the different modes of selection operating to maintain different morph patterns. The color polymorphic spiny-backed spider, Thelacantha brevispina, was surveyed on Moorea, French Polynesia to understand distribution, prey abundance, and density across coastal and forest habitats. In addition, split-brood and laboratory reciprocal transplant experiments were conducted to determine whether coloration was due to genes or a result of phenotypic plasticity. Quantitative field surveys revealed a negative relationship between spider density and prey abundance, with lower prey counts in coastal habitats but prey yielded higher energy value. Spiders were found on a variety of habitats with diverse prey species. The split-brood design showed that a genetic origin of coloration is likely with strong maternal effects and distinct color differences among sites. The reciprocal transplant confirmed the lack of a plastic response to rearing habitats. -
Phylogeny and Historical Biogeography of Geraniaceae In
Systematic Botany (2008), 33(2): pp. 326–342 © Copyright 2008 by the American Society of Plant Taxonomists Phylogeny and Historical Biogeography of Geraniaceae in Relation to Climate Changes and Pollination Ecology Omar Fiz, Pablo Vargas, Marisa Alarcón, Carlos Aedo, José Luis García, and Juan José Aldasoro1 Real Jardín Botanico de Madrid, CSIC, Plaza de Murillo 2, 28014 Madrid, Spain 1Author for correspondence ([email protected]) Communicating Editor: Mark P. Simmons Abstract—Chloroplast (trnL–F and rbcL) sequences were used to reconstruct the phylogeny of Geraniaceae and Hypseocharitaceae. According to these data Hypseocharitaceae and Geraniaceae are monophyletic. Pelargonium and Monsonia are sisters to the largest clade of Geraniaceae, formed by Geranium, Erodium and California. According to molecular dating and dispersal-vicariance analysis, the split of the stem branches of Geraniaceae probably occurred during the Oligocene, in southern Africa or in southern Africa plus the Mediterranean area. However, their diversification occurred during the Miocene, coinciding with the beginning of major aridification events in their distribution areas. An ancestor of the largest clade of Geraniaceae (Geranium, Erodium, and California) colonised a number of habitats in the northern hemisphere and in South American mountain ranges. In summary, the evolution of the Geraniaceae is marked by the dispersal of ancestors from Southern Africa to cold, temperate and often disturbed habitats in the rest of world, where only generalist pollination and facultative autogamy could ensure sufficient seed production and survival. Keywords—autocompatibility, dispersal-vicariance, drought-tolerance, molecular dating, nectaries, P/O indexes. The Geraniaceae are included in the order Geraniales along are characteristic of the Afro-Arabian land mass (Hutchin- with the families Francoaceae, Greyiaceae, Ledocarpaceae, son 1969). -
CRAZY CREEPY CRAWLERS Deadly Spiders by Matt Turner Illustrated by Santiago Calle
CRAZY CREEPY CRAWLERS Deadly Spiders By Matt Turner Illustrated by Santiago Calle Oh, what big eyes you have! THIS PAGE INTENTIONALLY LEFT BLANK CRAZY CREEPY CRAWLERS deadly Spiders anks to the creative team: Senior Editor: Alice Peebles Fact Checking: Kate Mitchell Designer: www.collaborate.agency Original edition copyright 2016 by Hungry Tomato Ltd. Copyright © 2017 by Lerner Publishing Group, Inc. Hungry Tomato™ is a trademark of Lerner Publishing Group, Inc. All rights reserved. International copyright secured. No part of this book may be reproduced, stored in a retrieval system, or transmitted in any form or by any means—electronic, mechanical, photocopying, recording, or otherwise—without the prior written permission of Lerner Publishing Group, Inc., except for the inclusion of brief deadly Spiders quotations in an acknowledged review. Hungry Tomato™ A division of Lerner Publishing Group, Inc. 241 First Avenue North Minneapolis, MN 55401 USA For reading levels and more information, look up this title at www.lernerbooks.com. Main body text set in Adobe Devanagari Regular 12/13. Typeface provided by Adobe Systems. Library of Congress Cataloging-in-Publication Data Names: Turner, Matt, 1964– , author. Title: Deadly spiders / Matt Turner. Description: Minneapolis : Hungry Tomato, 2017. | Includes index. | Audience: Ages 8 to 12. | Audience: Grades 4 to 6. Identi ers: LCCN 2016023370 (print) | LCCN 2016034753 (ebook) | ISBN 9781512415537 (lb : alk. paper) | ISBN 9781512430806 (pb : alk. paper) | ISBN 9781512427134 (eb pdf) Subjects: -
Book of Abstracts
August 20th-25th, 2017 University of Nottingham – UK with thanks to: Organising Committee Sara Goodacre, University of Nottingham, UK Dmitri Logunov, Manchester Museum, UK Geoff Oxford, University of York, UK Tony Russell-Smith, British Arachnological Society, UK Yuri Marusik, Russian Academy of Science, Russia Helpers Leah Ashley, Tom Coekin, Ella Deutsch, Rowan Earlam, Alastair Gibbons, David Harvey, Antje Hundertmark, LiaQue Latif, Michelle Strickland, Emma Vincent, Sarah Goertz. Congress logo designed by Michelle Strickland. We thank all sponsors and collaborators for their support British Arachnological Society, European Society of Arachnology, Fisher Scientific, The Genetics Society, Macmillan Publishing, PeerJ, Visit Nottinghamshire Events Team Content General Information 1 Programme Schedule 4 Poster Presentations 13 Abstracts 17 List of Participants 140 Notes 154 Foreword We are delighted to welcome you to the University of Nottingham for the 30th European Congress of Arachnology. We hope that whilst you are here, you will enjoy exploring some of the parks and gardens in the University’s landscaped settings, which feature long-established woodland as well as contemporary areas such as the ‘Millennium Garden’. There will be a guided tour in the evening of Tuesday 22nd August to show you different parts of the campus that you might enjoy exploring during the time that you are here. Registration Registration will be from 8.15am in room A13 in the Pope Building (see map below). We will have information here about the congress itself as well as the city of Nottingham in general. Someone should be at this registration point throughout the week to answer your Questions. Please do come and find us if you have any Queries.