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Diptera: Syrphidae
This is a repository copy of The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae).. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/80035/ Version: Accepted Version Article: Penney, HD, Hassall, C orcid.org/0000-0002-3510-0728, Skevington, JH et al. (2 more authors) (2014) The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae). The American Naturalist, 183 (2). pp. 281-289. ISSN 0003-0147 https://doi.org/10.1086/674612 Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ The relationship between morphological and behavioral mimicry in hover flies (Diptera: Syrphidae)1 Heather D. Penney, Christopher Hassall, Jeffrey H. Skevington, Brent Lamborn & Thomas N. Sherratt Abstract Palatable (Batesian) mimics of unprofitable models could use behavioral mimicry to compensate for the ease with which they can be visually discriminated, or to augment an already close morphological resemblance. -
Biodiversity Climate Change Impacts Report Card Technical Paper 12. the Impact of Climate Change on Biological Phenology In
Sparks Pheno logy Biodiversity Report Card paper 12 2015 Biodiversity Climate Change impacts report card technical paper 12. The impact of climate change on biological phenology in the UK Tim Sparks1 & Humphrey Crick2 1 Faculty of Engineering and Computing, Coventry University, Priory Street, Coventry, CV1 5FB 2 Natural England, Eastbrook, Shaftesbury Road, Cambridge, CB2 8DR Email: [email protected]; [email protected] 1 Sparks Pheno logy Biodiversity Report Card paper 12 2015 Executive summary Phenology can be described as the study of the timing of recurring natural events. The UK has a long history of phenological recording, particularly of first and last dates, but systematic national recording schemes are able to provide information on the distributions of events. The majority of data concern spring phenology, autumn phenology is relatively under-recorded. The UK is not usually water-limited in spring and therefore the major driver of the timing of life cycles (phenology) in the UK is temperature [H]. Phenological responses to temperature vary between species [H] but climate change remains the major driver of changed phenology [M]. For some species, other factors may also be important, such as soil biota, nutrients and daylength [M]. Wherever data is collected the majority of evidence suggests that spring events have advanced [H]. Thus, data show advances in the timing of bird spring migration [H], short distance migrants responding more than long-distance migrants [H], of egg laying in birds [H], in the flowering and leafing of plants[H] (although annual species may be more responsive than perennial species [L]), in the emergence dates of various invertebrates (butterflies [H], moths [M], aphids [H], dragonflies [M], hoverflies [L], carabid beetles [M]), in the migration [M] and breeding [M] of amphibians, in the fruiting of spring fungi [M], in freshwater fish migration [L] and spawning [L], in freshwater plankton [M], in the breeding activity among ruminant mammals [L] and the questing behaviour of ticks [L]. -
Final Report 1
Sand pit for Biodiversity at Cep II quarry Researcher: Klára Řehounková Research group: Petr Bogusch, David Boukal, Milan Boukal, Lukáš Čížek, František Grycz, Petr Hesoun, Kamila Lencová, Anna Lepšová, Jan Máca, Pavel Marhoul, Klára Řehounková, Jiří Řehounek, Lenka Schmidtmayerová, Robert Tropek Březen – září 2012 Abstract We compared the effect of restoration status (technical reclamation, spontaneous succession, disturbed succession) on the communities of vascular plants and assemblages of arthropods in CEP II sand pit (T řebo ňsko region, SW part of the Czech Republic) to evaluate their biodiversity and conservation potential. We also studied the experimental restoration of psammophytic grasslands to compare the impact of two near-natural restoration methods (spontaneous and assisted succession) to establishment of target species. The sand pit comprises stages of 2 to 30 years since site abandonment with moisture gradient from wet to dry habitats. In all studied groups, i.e. vascular pants and arthropods, open spontaneously revegetated sites continuously disturbed by intensive recreation activities hosted the largest proportion of target and endangered species which occurred less in the more closed spontaneously revegetated sites and which were nearly absent in technically reclaimed sites. Out results provide clear evidence that the mosaics of spontaneously established forests habitats and open sand habitats are the most valuable stands from the conservation point of view. It has been documented that no expensive technical reclamations are needed to restore post-mining sites which can serve as secondary habitats for many endangered and declining species. The experimental restoration of rare and endangered plant communities seems to be efficient and promising method for a future large-scale restoration projects in abandoned sand pits. -
Publications Files/2011 Dapporto Et Al Pyronia.Pdf
Journal of Biogeography (J. Biogeogr.) (2011) 38, 854–867 ORIGINAL Phylogenetic island disequilibrium: ARTICLE evidence for ongoing long-term population dynamics in two Mediterranean butterflies Leonardo Dapporto1*, Thomas Schmitt2, Roger Vila3, Stefano Scalercio4, Heinrich Biermann5, Vlad Dinca˘6,7, Severiano F. Gayubo8, Jose´ A. Gonza´lez8, Pietro Lo Cascio9 and Roger L. H. Dennis10,11 1Istituto Comprensivo Materna Elementere ABSTRACT Media Convenevole da Prato via 1° Maggio 40, Aim Our aims were to verify the existence of phylogenetic disequilibrium 59100 Prato, Italy, 2Department of Biogeography, Trier University, D-54296 Trier, between butterfly lineages at the subcontinental scale for islands and the nearest Germany, 3ICREA and Institute of mainland and to test the capacity of islands for hosting ancestral populations of Evolutionary Biology (CSIC-UPF), Passeig butterflies and the significance of such relict populations. Marı´tim de la Barceloneta 37-49, 08003 Location The western Mediterranean continental area of Europe and North 4 Barcelona, Spain, CRA Centro di Ricerca per Africa together with several large and small islands (Balearics, Tuscan l’Olivicoltura e l’Industria Olearia, I-87036 Archipelago, Aeolian Archipelago, Capri, Sardinia, Sicily, Corsica). Rende (Cosenza), Italy, 5Markusstrasse 17, D-3490, Bad Driburg, Germany, 6Institute of Methods Using geometric morphometrics, the shape of male genitalia was Evolutionary Biology (CSIC-UPF), Passeig analysed in two common butterflies (Pyronia cecilia and Pyronia tithonus), whose Marı´tim de la Barceloneta 37-49, 08003 spatial heterogeneity in the Mediterranean region has recently been described. Barcelona, Spain, 7Departament de Gene`tica i Observed patterns in genital shapes were compared with shapes predicted for Microbiologia, Universitat Auto`noma de islands and fossil islands to assess the contribution of historical and current events Barcelona, 08193 Bellaterra (Barcelona), in accounting for the transition from a refugial model to an equilibrium model. -
Butterfly Anatomy [Online]
02 July 2015 (original version 01 January 2014) © Peter Eeles Citation: Eeles, P. (2015). Butterfly Anatomy [Online]. Available from http://www.dispar.org/reference.php?id=6 [Accessed July 2, 2015]. Butterfly Anatomy Peter Eeles This paper contains a condensed summary on the anatomy of the imago (adult), ovum (egg), larva (caterpillar) and pupa (chrysalis). Many of the features discussed on this page are referred to from the taxonomy section of the UK Butterflies website since they are used in butterfly classification. Imago The body of the adult butterfly is comprised of 3 segments - head, thorax and abdomen. The eyes, antennae, proboscis and palpi are all positioned on the head. The legs and wings are attached to the thorax. The reproductive organs and spiracles are part of the abdomen. All of these features are discussed in detail below and the illustrations below provide an overview of the majority of these features. Chequered Skipper (Carterocephalus palaemon) Photo © Pete Eeles Eyes The head contains a pair of compound eyes, each made up of a large number of photoreceptor units known as ommatidia. Each ommatidium includes a lens (the front of which makes up a single facet at the surface of the eye), light-sensitive visual cells and also cells that separate the ommatidium from its neighbours. The image below shows a closeup of the head of a Pyralid moth, clearly showing the facets on the surface of the eye. A butterfly is able to build up a complete picture of its surroundings by synthesising an image from the individual inputs provided by each ommatidium. -
The Bulletin of Zoological Nomenclature V57 Part02
Volume 57, Part 2, 30 June 2000, pp. 69-136 ISSN 0007-5167 stum The Bulletin of Zoological Nomenclature Original from and digitized by National University of Singapore Libraries THE BULLETIN OF ZOOLOGICAL NOMENCLATURE The Bulletin is published four times a year for the International Commission on Zoological Nomenclature by the International Trust for Zoological Nomenclature, a charity (no. 211944) registered in England. The annual subscription for 2000 is £110 or $200, postage included. All manuscripts, letters and orders should be sent to: The Executive Secretary, International Commission on Zoological Nomenclature, c/o The Natural History Museum, Cromwell Road, London, SW7 5BD, U.K. (Tel. 020 7942 5653) (e-mail: [email protected]) (http://www.iczn.org) INTERNATIONAL COMMISSION ON ZOOLOGICAL NOMENCLATURE Officers President Prof A. Minelli {Italy) Vice-President Dr W. N. Eschmeyer (U.S.A.) Executive Secretary Dr P. K. Tubbs (United Kingdom) Members Prof W. J. Bock (U.S.A.; Ornithology) Dr V. Mahnert Prof P. Bouchet (France; Mollusca) (Switzerland; Ichthyology) Prof D. J. Brothers Prof U. R. Martins de Souza (South Africa; Hymenoptera) (Brazil; Coleoptera) Dr L. R. M. Cocks (U.K.; Brachiopoda) Prof S. F. Mawatari (Japan; Bryozoa) DrH.G. Cogger (Australia; Herpetology) Prof A. Minelli (Italy; Myriapoda) Prof C. Dupuis (France; Heteroptera) Dr C. Nielsen (Denmark; Bryozoa) Dr W. N. Eschmeyer Dr L. Papp (Hungary; Diptera) (U.S.A.; Ichthyology) Prof D. J. Patterson (Australia; Protista) Mr D. Heppell (U.K.; Mollusca) Prof W. D. L. Rid^(Australia; Mammalia) Dr I. M. Kerzhner (Russia; Heteroptera) Prof J. M. Savage (U.S. A; Herpetology) Prof Dr O. -
Hoverflies: the Garden Mimics
Article Hoverflies: the garden mimics. Edmunds, Malcolm Available at http://clok.uclan.ac.uk/1620/ Edmunds, Malcolm (2008) Hoverflies: the garden mimics. Biologist, 55 (4). pp. 202-207. ISSN 0006-3347 It is advisable to refer to the publisher’s version if you intend to cite from the work. For more information about UCLan’s research in this area go to http://www.uclan.ac.uk/researchgroups/ and search for <name of research Group>. For information about Research generally at UCLan please go to http://www.uclan.ac.uk/research/ All outputs in CLoK are protected by Intellectual Property Rights law, including Copyright law. Copyright, IPR and Moral Rights for the works on this site are retained by the individual authors and/or other copyright owners. Terms and conditions for use of this material are defined in the policies page. CLoK Central Lancashire online Knowledge www.clok.uclan.ac.uk Hoverflies: the garden mimics Mimicry offers protection from predators by convincing them that their target is not a juicy morsel after all. it happens in our backgardens too and the hoverfly is an expert at it. Malcolm overflies are probably the best the mimic for the model and do not attack Edmunds known members of tbe insect or- it (Edmunds, 1974). Mimicry is far more Hder Diptera after houseflies, blue widespread in the tropics than in temperate bottles and mosquitoes, but unlike these lands, but we have some of the most superb insects they are almost universally liked examples of mimicry in Britain, among the by the general public. They are popular hoverflies. -
Pollinator Portraits 2017 Portraits De Pollinisateurs 2017
Pollinator Portraits 2017 Photos: © Martin C D Speight Text: Martin C D Speight This guide has been assembled by the National Biodiversity Data Centre Pollinator portraits 2017 These portraits are not of bees, but of flies – European hoverflies, to be precise. In the landscape, hoverflies are small and can flit by unobserved. In the portraits we see them larger than life and can examine them at leisure. You are invited to send the portraits to friends and colleagues. Not so well known as bees, hoverflies play their own, and slightly different role in pollination. They are significant pollinators of various fruit trees and some other crops, like oil-seed rape. They also pollinate many wild flowers, including rare species not normally visited by bees. Hoverflies can be found in a very wide range of terrestrial and freshwater habitats. As larvae about a third of them feed on greenfly, other plant bugs, or small caterpillars and are recognised as helping to prevent epidemic greenfly infestations in cereal crops like winter wheat. Another equally large group of species is plant-feeding; these hoverflies mine leaves, stem- bases, rhizomes, tubers, bulbs or corms of herb layer plants. The rest of them grow up on a diet of bacteria, algae or other micro-organisms, usually in water or damp situations of some sort. Almost without exception, as adults hoverflies feed on nectar and pollen, visiting the flowers of a very wide range of trees, shrubs and herb layer plants, including pollen-only flowers like those of grasses, sedges, oak trees and poppies. The names of the hoverflies depicted in each portrait, along with brief notes, are included at the end of this document. -
Evidence from European Butterfly Sister Species
bioRxiv preprint doi: https://doi.org/10.1101/2020.09.04.282962; this version posted November 3, 2020. 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 The Pleistocene species pump past its prime: 2 evidence from European butterfly sister species 1 1 2 3 Sam Ebdon* , Dominik R. Laetsch , Leonardo Dapporto , 3 4 5 4 Alexander Hayward , Michael G. Ritchie , Vlad Dinc˘a , Roger 6 1 5 Vila , and Konrad Lohse 1 6 Institute of Evolutionary Biology, University of Edinburgh, 7 Edinburgh, EH9 3FL, UK 2 8 ZEN lab, Dipartimento di Biologia dell'Universit`adi Firenze, 9 Firenze, Italy 3 10 Centre for Ecology and Conservation, University of Exeter, 11 Penryn Campus, Cornwall, TR10 9FE, UK 4 12 Centre for Biological Diversity, School of Biology, University of St 13 Andrews, Fife KY16 9TH, UK 5 14 Ecology and Genetics Research Unit, University of Oulu, Oulu, 15 Finland 6 16 Institut de Biologia Evolutiva (CSIC - Universitat Pompeu 17 Fabra), Passeig Mar´ıtimde la Barceloneta 37, ESP-08003 18 Barcelona, Spain 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.09.04.282962; this version posted November 3, 2020. 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. -
Page 1 ^ '~£L Jp % I-Il- R J
'~£l ^ jP % ' C i-il- r j ^ - 4 ^V z% b<W- ?^ Is J) $& r^s V? Return to LIBRARY OF MARINE BIOLOGICAL LABORATORY WOODS HOLE, MASS. Loaned by American Museum of Natural History )^ ^AJlAAAu THE CANADIAN LIBRARY ENTOMOLOGIST. fee. ^K VOLUME III. m& WITIX FORTY ILLUSTRATION'S. (gbiteb bij the llicb. <£. J. £. Methane, itt. 1., Head Master of Trinity College School, Port Hope, Ont. ISBIST£D i:\ J. M, W. B. Ont. ; and SAUNDERB, London, Ont. ; E. REED, Bari-istei'-at-Law, London, DENTON, London, Ont, LONDON : PRINTED BY THE FREE PRESS STEAM PRINTING COMPANY. RICHMOND S'l I 87 r -5 rr LIST OF CONTRIBUTORS TO THIS VOLUME. BETHUNE, REV. C. J. S., The Editor Port Hope, Ont. B< >WLES, G. J Quebec. CHAMBERS, V. T Covington, Rv. ( :OU PER, WM Montreal, P. Q. ]). ! )ODGE, C. R Washington, C, U. S. )I I M M( )CK, GEO Springfield, Mass., U. S. t EDWARDS, W. H Coalburgh, W . Va., U. S. GROTE, AUG. R Demopolis, Ala, U. S. JONES, J. MATTHEW Halifax, Nova Scotia. PARKER. H. W Amherst, Mass., U. S. PETTIT, J Grimsby, Ont. REED, E. B.j Assistant Editor London, Ont. RILEY, C. V ST. Louis, Mo., U. S. SAUNDERS, WM., Assistant Editor London, Ont. SPRAGUE, P. S Boston, Mass., U. S. THOMAS, C Washington, D. C, U.S. WALKER, FRANCIS London, England. V < J ( ) X S T I T XT T I() N OP INCORPORATED 1871. SECTION I.— (OBJECTS AND MEMBERSHIP.) " 1. The Society shall be called The Entomological Society of Ontario/' and is instituted for the investigation of the character and habits of insects, the improve- ment and advancement of Entomological Science, and more especially its practical bearing on the Agricultural and Horticultural interests of the Province. -
Coleoptera, Chrysomelidae) in Azerbaijan
Turk J Zool 25 (2001) 41-52 © T†BÜTAK A Study of the Ecofaunal Complexes of the Leaf-Eating Beetles (Coleoptera, Chrysomelidae) in Azerbaijan Nailya MIRZOEVA Institute of Zoology, Azerbaijan Academy of Sciences, pr. 1128, kv. 504, Baku 370073-AZERBAIJAN Received: 01.10.1999 Abstract: A total of 377 leaf-eating beetle species from 69 genera and 11 subfamilies (Coleoptera, Chrysomelidae) were revealed in Azerbaijan, some of which are important pests of agriculture and forestry. The leaf-eating beetle distribution among different areas of Azerbaijan is presented. In the Great Caucasus 263 species are noted, in the Small Caucasus 206, in Kura - Araks lowland 174, and in Lenkoran zone 262. The distribution of the leaf-eating beetles among different sites is also described and the results of zoogeographic analysis of the leaf-eating beetle fauna are presented as well. Eleven zoogeographic groups of the leaf-eating beetles were revealed in Azerbaijan, which are not very specific. The fauna consists mainly of the common species; the number of endemic species is small. Key Words: leaf-eating beetle, larva, pest, biotope, zoogeography. AzerbaycanÕda Yaprak Bšcekleri (Coleoptera, Chrysomelidae) FaunasÝ †zerinde AraßtÝrmalar …zet: AzerbeycanÕda 11 altfamilyadan 69 cinse ait 377 YaprakbšceÛi (Col.: Chrysomelidae) tŸrŸ belirlenmißtir. Bu bšceklerden bazÝlarÝ tarÝm ve orman alanlarÝnda zararlÝ durumundadÝr. Bu •alÝßmada YaprakbšcekleriÕnin AzerbeycanÕÝn deÛißik bšlgelerindeki daÛÝlÝßlarÝ a•ÝklanmÝßtÝr. BŸyŸk KafkasyaÕda 263, KŸ•Ÿk KafkasyaÕda 206, KŸr-Aras ovasÝnda 174, Lenkaran BšlgesiÕnde ise 262 tŸr bulunmußtur. Bu tŸrlerin farklÝ biotoplardaki durumu ve daÛÝlÝßlarÝ ile ilgili zoocografik analizleride bu •alÝßmada yer almaktadÝr. AzerbeycanÕda belirlenen Yaprakbšcekleri 11 zoocografik grupda incelenmißtir. YapÝlan bu fauna •alÝßmasÝnda belirlenen tŸrlerin bir•oÛu yaygÝn olarak bulunan tŸrlerdir, endemik tŸr sayÝsÝ olduk•a azdÝr. -
Lepidoptera: Noctuoidea: Erebidae) and Its Phylogenetic Implications
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 113: 558–570, 2016 http://www.eje.cz doi: 10.14411/eje.2016.076 ORIGINAL ARTICLE Characterization of the complete mitochondrial genome of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) and its phylogenetic implications YU SUN, SEN TIAN, CEN QIAN, YU-XUAN SUN, MUHAMMAD N. ABBAS, SAIMA KAUSAR, LEI WANG, GUOQING WEI, BAO-JIAN ZHU * and CHAO-LIANG LIU * College of Life Sciences, Anhui Agricultural University, 130 Changjiang West Road, Hefei, 230036, China; e-mails: [email protected] (Y. Sun), [email protected] (S. Tian), [email protected] (C. Qian), [email protected] (Y.-X. Sun), [email protected] (M.-N. Abbas), [email protected] (S. Kausar), [email protected] (L. Wang), [email protected] (G.-Q. Wei), [email protected] (B.-J. Zhu), [email protected] (C.-L. Liu) Key words. Lepidoptera, Noctuoidea, Erebidae, Spilarctia robusta, phylogenetic analyses, mitogenome, evolution, gene rearrangement Abstract. The complete mitochondrial genome (mitogenome) of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) was se- quenced and analyzed. The circular mitogenome is made up of 15,447 base pairs (bp). It contains a set of 37 genes, with the gene complement and order similar to that of other lepidopterans. The 12 protein coding genes (PCGs) have a typical mitochondrial start codon (ATN codons), whereas cytochrome c oxidase subunit 1 (cox1) gene utilizes unusually the CAG codon as documented for other lepidopteran mitogenomes. Four of the 13 PCGs have incomplete termination codons, the cox1, nad4 and nad6 with a single T, but cox2 has TA. It comprises six major intergenic spacers, with the exception of the A+T-rich region, spanning at least 10 bp in the mitogenome.