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Based on Comparative Morphological Data AF Emel'yanov Transactions of T
The phylogeny of the Cicadina (Homoptera, Cicadina) based on comparative morphological data A.F. Emel’yanov Transactions of the All-Union Entomological Society Morphological principles of insect phylogeny The phylogenetic relationships of the principal groups of cicadine* insects have been considered on more than one occasion, commencing with Osborn (1895). Some phylogenetic schemes have been based only on data relating to contemporary cicadines, i.e. predominantly on comparative morphological data (Kirkaldy, 1910; Pruthi, 1925; Spooner, 1939; Kramer, 1950; Evans, 1963; Qadri, 1967; Hamilton, 1981; Savinov, 1984a), while others have been constructed with consideration given to paleontological material (Handlirsch, 1908; Tillyard, 1919; Shcherbakov, 1984). As the most primitive group of the cicadines have been considered either the Fulgoroidea (Kirkaldy, 1910; Evans, 1963), mainly because they possess a small clypeus, or the cicadas (Osborn, 1895; Savinov, 1984), mainly because they do not jump. In some schemes even the monophyletism of the cicadines has been denied (Handlirsch, 1908; Pruthi, 1925; Spooner, 1939; Hamilton, 1981), or more precisely in these schemes the Sternorrhyncha were entirely or partially depicted between the Fulgoroidea and the other cicadines. In such schemes in which the Fulgoroidea were accepted as an independent group, among the remaining cicadines the cicadas were depicted as branching out first (Kirkaldy, 1910; Hamilton, 1981; Savinov, 1984a), while the Cercopoidea and Cicadelloidea separated out last, and in the most widely acknowledged systematic scheme of Evans (1946b**) the last two superfamilies, as the Cicadellomorpha, were contrasted to the Cicadomorpha and the Fulgoromorpha. At the present time, however, the view affirming the equivalence of the four contemporary superfamilies and the absence of a closer relationship between the Cercopoidea and Cicadelloidea (Evans, 1963; Emel’yanov, 1977) is gaining ground. -
Dipterists Digest
Dipterists Digest 2019 Vol. 26 No. 1 Cover illustration: Eliozeta pellucens (Fallén, 1820), male (Tachinidae) . PORTUGAL: Póvoa Dão, Silgueiros, Viseu, N 40º 32' 59.81" / W 7º 56' 39.00", 10 June 2011, leg. Jorge Almeida (photo by Chris Raper). The first British record of this species is reported in the article by Ivan Perry (pp. 61-62). Dipterists Digest Vol. 26 No. 1 Second Series 2019 th Published 28 June 2019 Published by ISSN 0953-7260 Dipterists Digest Editor Peter J. Chandler, 606B Berryfield Lane, Melksham, Wilts SN12 6EL (E-mail: [email protected]) Editorial Panel Graham Rotheray Keith Snow Alan Stubbs Derek Whiteley Phil Withers Dipterists Digest is the journal of the Dipterists Forum . It is intended for amateur, semi- professional and professional field dipterists with interests in British and European flies. All notes and papers submitted to Dipterists Digest are refereed. Articles and notes for publication should be sent to the Editor at the above address, and should be submitted with a current postal and/or e-mail address, which the author agrees will be published with their paper. Articles must not have been accepted for publication elsewhere and should be written in clear and concise English. Contributions should be supplied either as E-mail attachments or on CD in Word or compatible formats. The scope of Dipterists Digest is: - the behaviour, ecology and natural history of flies; - new and improved techniques (e.g. collecting, rearing etc.); - the conservation of flies; - reports from the Diptera Recording Schemes, including maps; - records and assessments of rare or scarce species and those new to regions, countries etc.; - local faunal accounts and field meeting results, especially if accompanied by ecological or natural history interpretation; - descriptions of species new to science; - notes on identification and deletions or amendments to standard key works and checklists. -
Called “Talking Animals” Taught Us About Human Language?
Linguistic Frontiers • 1(1) • 14-38 • 2018 DOI: 10.2478/lf-2018-0005 Linguistic Frontiers Representational Systems in Zoosemiotics and Anthroposemiotics Part I: What Have the So- Called “Talking Animals” Taught Us about Human Language? Research Article Vilém Uhlíř* Theoretical and Evolutionary Biology, Department of Philosophy and History of Sciences. Charles University. Viničná 7, 12843 Praha 2, Czech Republic Received ???, 2018; Accepted ???, 2018 Abstract: This paper offers a brief critical review of some of the so-called “Talking Animals” projects. The findings from the projects are compared with linguistic data from Homo sapiens and with newer evidence gleaned from experiments on animal syntactic skills. The question concerning what had the so-called “Talking Animals” really done is broken down into two categories – words and (recursive) syntax. The (relative) failure of the animal projects in both categories points mainly to the fact that the core feature of language – hierarchical recursive syntax – is missing in the pseudo-linguistic feats of the animals. Keywords: language • syntax • representation • meta-representation • zoosemiotics • anthroposemiotics • talking animals • general cognition • representational systems • evolutionary discontinuity • biosemiotics © Sciendo 1. The “Talking Animals” Projects For the sake of brevity, I offer a greatly selective review of some of the more important “Talking Animals” projects. Please note that many omissions were necessary for reasons of space. The “thought climate” of the 1960s and 1970s was formed largely by the Skinnerian zeitgeist, in which it seemed possible to teach any animal to master any, or almost any, skill, including language. Perhaps riding on an ideological wave, following the surprising claims of Fossey [1] and Goodall [2] concerning primates, as well as the claims of Lilly [3] and Batteau and Markey [4] concerning dolphins, many scientists and researchers focussed on the continuities between humans and other species, while largely ignoring the discontinuities and differences. -
Musical Pluralism and the Science of Music Anton Killin & Adrian Currie Penultimate Version, Forthcoming in the European
Musical pluralism and the science of music Anton Killin & Adrian Currie Penultimate version, forthcoming in the European Journal for Philosophy of Science Abstract: The scientific investigation of music requires contributions from a diverse array of disciplines (e.g. anthropology, musicology, neuroscience, psychology, music theory, music therapy, sociology, computer science, evolutionary biology, archaeology, acoustics and philosophy). Given the diverse methodologies, interests and research targets of the disciplines involved, we argue that there is a plurality of legitimate research questions about music, necessitating a focus on integration. In light of this we recommend a pluralistic conception of music—that there is no unitary definition divorced from some discipline, research question or context. This has important implications for how the scientific study of music ought to proceed: we show that some definitions are complementary, that is, they reflect different research interests and ought to be retained and, where possible, integrated, while others are antagonistic, they represent real empirical disagreement about music’s nature and how to account for it. We illustrate this in discussion of two related issues: questions about the evolutionary function (if any) of music, and questions of the innateness (or otherwise) of music. These debates have been, in light of pluralism, misconceived. We suggest that, in both cases, scientists ought to proceed by constructing integrated models which take into account the dynamic interaction between different aspects of music. Keywords: Definitions of music; musicality; pluralism; musical cognition; evolution of music. 1. Introduction Music is a complex and fascinating target of scientific inquiry. Nevertheless, theorists disagree on what music is—on how best to characterise or define it (see e.g. -
Dermaptera, Forficulidae)
Dtsch. Entomol. Z. 68 (2) 2021, 235–248 | DOI 10.3897/dez.68.68020 The Pyrenean species of Chelidura (Dermaptera, Forficulidae) Pilar Jurado-Angulo1, Yolanda Jiménez-Ruiz1, Mario García-París1 1 Department of Biodiversity and Evolutionary Biology. Museo Nacional de Ciencias Naturales, MNCN-CSIC. c/ José Gutiérrez Abascal, 2. 28006, Madrid. Spain http://zoobank.org/43AD7562-7AF5-426D-A7EF-17225DD9AD98 Corresponding author: Pilar Jurado-Angulo ([email protected]) Academic editor: Susanne Randolf ♦ Received 28 April 2021 ♦ Accepted 6 July 2021 ♦ Published 10 August 2021 Abstract The Pyrenees are inhabited by scattered populations of earwigs of the genus Chelidura Latreille, 1825. There is some controversy about the specific assignment of these populations: while most authors assign them toC. pyrenaica (Gené, 1832), other consider that C. aptera (Mégerlé, 1825) is also present in the Pyrenees. The main objective of this work was to revise the identity and synonyms of Pyrenean Chelidura. Specimens from recent fieldwork and collections (MNCN-CSIC) were used for morphological and molecular studies (cytochrome oxidase 1). All Pyrenean specimens shared similar cox1 sequences, very divergent from those of Alpine C. ap- tera. As a consequence, the variability observed in male cerci morphology from the Pyrenees, ranging from long and slightly curved to short and very curved, corresponded to C. pyrenaica, and the presence of C. aptera in the Pyrenees can be rejected. As previously suggested by Maccagno (1933) and Fontana et al. (2021), the revision of the synonymic list uncovered the misplacement of the name F. simplex Germar, 1825 under the synonymy of C. aptera, while it rather represents a synonym of C. -
N E W S L E T T E R
Entomological Society of Victoria N e w s l e t t e r No. 1 February 2014 INDEX Welcome to the Entomological Society of Victoria newsletter Welcome…………...…1 The ESV has a long and distinguished 87-year history of contributing to Visit to AgriBio, knowledge of, and the promotion of, Victorian insects, beginning in the 1920s: Bundoora (photos)…..2 “On April 5, 1927 fourteen people interested in entomology met at the East Malvern home of the late Mr F.E. Wilson for the purpose of forming an Meet your ESV Council entomological club...” (part one)…..…………3 So began The Entomologists’ Club, now known as the Entomological Society of Victorian Alps Bioscan Victoria. The focus of the early years of the club were “excursions – rambles (photos)……………….4 they are often called in the Minutes – made to places such as Heathmont, Millgrove, Frankston, Ringwood, Blackburn, Noble Park and Ferntree Gully.” For sale……………….5 “Membership of the Society in the years 1927-1940 was from 25 to 40, although Australian attendance at meetings fell to a very low ebb at times...Because of the Entomological pressures of the war the Society lapsed about 1942 and was not re-established Conferences………….5 until 1961 when Mr J.C. Le Soeuf arranged a meeting at the National Herbarium Hall for this purpose.” Around the Societies...5 Today’s membership is consistently over 100, continuing the tradition of excursions, publications, presentations and the general promotion of all things Bugs in profile………..6 entomological. Le Soeuf is commemorated with the award named in his honour, most recently awarded to Peter Marriott, the Society’s Immediate Past International President. -
UNIVERSITÀ DEGLI STUDI DEL MOLISE Department
UNIVERSITÀ DEGLI STUDI DEL MOLISE Department of Agricultural, Environmental and Food Sciences Ph.D. course in: AGRICULTURE TECHNOLOGY AND BIOTECHNOLOGY (CURRICULUM: Sustainable plant production and protection) (CYCLE XXIX) Ph.D. thesis NEW INSIGHTS INTO THE BIOLOGY AND ECOLOGY OF THE INSECT VECTORS OF APPLE PROLIFERATION FOR THE DEVELOPMENT OF SUSTAINABLE CONTROL STRATEGIES Coordinator of the Ph.D. course: Prof. Giuseppe Maiorano Supervisor: Prof. Antonio De Cristofaro Co-Supervisor: Dr. Claudio Ioriatti Ph.D. student: Tiziana Oppedisano Matr: 151603 2015/2016 “Nella vita non c’è nulla da temere, c’è solo da capire.” (M. Curie) Index SUMMARY 5 RIASSUNTO 9 INTRODUCTION 13 Phytoplasmas 13 Taxonomy 13 Morphology 14 Symptomps 15 Transmission and spread 15 Detection 17 Phytoplasma transmission by insect vectors 17 Phytoplasma-vector relationship 18 Homoptera as vectors of phytoplasma 19 ‘Candidatus Phytoplasma mali’ 21 Symptomps 21 Distribution in the tree 22 Host plant 24 Molecular characterization and diagnosis 24 Geographical distribution 25 AP in Italy 25 Transmission of AP 27 Psyllid vectors of ‘Ca. P. mali’ 28 Cacopsylla picta Förster (1848) 29 Cacopsylla melanoneura Förster (1848) 32 Other known vectors 36 Disease control 36 Aims of the research 36 References 37 CHAPTER 1: Apple proliferation in Valsugana: three years of disease and psyllid vectors’ monitoring 49 CHAPTER 2: Evaluation of the current vectoring efficiency of Cacopsylla melanoneura and Cacopsylla picta in Trentino 73 CHAPTER 3: The insect vector Cacopsylla picta vertically -
THE LITTLE THINGS THAT RUN the CITY 30 AMAZING INSECTS THAT LIVE in MELBOURNE! © City of Melbourne 2017 First Published May, 2017 ISBN 978-1-74250-900-6
THE littleTHINGS that run the city BY KATE CRANNEY, SARAH BEKESSY AND LUIS MATA In partnership with City of Melbourne 30 amazing insects that live in Melbourne! THE LITTLE THINGS THAT RUN THE CITY 30 AMAZING INSECTS THAT LIVE IN MELBOURNE! © City of Melbourne 2017 First published May, 2017 ISBN 978-1-74250-900-6 ABOUT THIS PROJECT This book is an outreach educational resource prepared by Kate Cranney, Sarah Bekessy and Luis Mata for the City of Melbourne. Kate, Sarah and Luis work as part of the Interdisciplinary Conservation Science Research Group at RMIT University in Melbourne, Australia. THE Illustrations: Kate Cranney Ink on paper, www.katecranney.com Photographs: Luis Mata flickr.com/photos/dingilingi/ Graphic Design: Kathy Holowko THANK YOU We wish to acknowledge the support of the Australian Government’s little National Environmental Science Programme - Clean Air and Urban THINGS Landscapes and Threatened Species Hubs, and the Australian Research Council Centre of Excellence for Environmental Decisions. The book was inspired by ‘The Little Things that Run the City – Insect ecology, biodiversity and conservation in the that run the city City of Melbourne’ research project (Mata et al. 2016). We are very grateful to the Australian Museum (http://australianmuseum.net.au/insects), the Museum Victoria BY KATE CRANNEY, SARAH BEKESSY AND LUIS MATA (https://museumvictoria.com.au/bugs/), the CSIRO’s ‘What Bug is That’ program (http://anic.ento.csiro.au/insectfamilies/) In partnership with City of Melbourne and ‘The Insects of Australia - A textbook for students and research workers’ book (Naumann et al. 1991). Thank you to Dr. -
Dominant Frequency Characteristics of Calling Songs in Cicada
Journal of Entomology and Zoology Studies 2014; 2 (6): 330-332 ISSN 2320-7078 Dominant frequency characteristics of calling songs in JEZS 2014; 2 (6): 330-332 © 2014 JEZS cicada Chloropsalta smaragdula Haupt, 1920 (Hem: www.entomoljournal.com Received: 21-10-2014 Cicadidae) and its relationship with body length, width, Accepted: 21-11-2014 and weight. Akbar Mohammadi-Mobarakeh Department of Entomology, Khorasgan (Isfahan) Branch, Islamic Azad University, Isfahan, Akbar Mohammadi-Mobarakeh, Bijan Hatami, Alireza Jalali Zand, Iran, 00989132375720. Rassoul Amir Fattahi, Hossein Zamanian Bijan Hatami Abstract Department of Entomology, To study the calling songs in cicada Chloropsalta smaragdula and its relationship with body length, Khorasgan (Isfahan) Branch, width, and weight, a research was conducted in the Iranian city of Mobarakeh, Isfahan Province, in 2011- Islamic Azad University, Isfahan, 2012. Different sound samples were taken under field and laboratory conditions. Throughout the Iran. sampling period, the calling songs of nine male cicadas were recorded and studied. The sound of each individual cicada was separately analyzed by MATLAB Software, and the size of its main parameter Alireza Jalali Zand Department of Entomology, (i.e., dominant frequency) was determined and recorded. The results showed that this cicada species have Khorasgan (Isfahan) Branch, a mean dominant frequency of 9.121 kHz. Moreover, the correlation coefficients indicated that there is a Islamic Azad University, Isfahan, positive relationship between the dominant frequency for the audio signal of the calling songs with body Iran. width and weight, and is significant at p<0.0001 probability level, thus, indicating that dominant frequency increases as body width and weight increase. -
Sound Radiation by the Bladder Cicada Cystosoma Saundersii
The Journal of Experimental Biology 201, 701–715 (1998) 701 Printed in Great Britain © The Company of Biologists Limited 1998 JEB1166 SOUND RADIATION BY THE BLADDER CICADA CYSTOSOMA SAUNDERSII H. C. BENNET-CLARK1,* AND D. YOUNG2 1Department of Zoology, Oxford University, South Parks Road, Oxford, OX1 3PS, UK and 2Department of Zoology, University of Melbourne, Parkville, Victoria 3052, Australia *e-mail: [email protected] Accepted 26 November 1997: published on WWW 5 February 1998 Summary Male Cystosoma saundersii have a distended thin-walled air sac volume was the major compliant element in the abdomen which is driven by the paired tymbals during resonant system. Increasing the mass of tergite 4 and sound production. The insect extends the abdomen from a sternites 4–6 also reduced the resonant frequency of the rest length of 32–34 mm to a length of 39–42 mm while abdomen. By extrapolation, it was shown that the effective singing. This is accomplished through specialised mass of tergites 3–5 was between 13 and 30 mg and that the apodemes at the anterior ends of abdominal segments 4–7, resonant frequency was proportional to 1/√(total mass), which cause each of these intersegmental membranes to suggesting that the masses of the tergal sound-radiating unfold by approximately 2 mm. areas were major elements in the resonant system. The calling song frequency is approximately 850 Hz. The The tymbal ribs buckle in sequence from posterior (rib song pulses have a bimodal envelope and a duration of 1) to anterior, producing a series of sound pulses. -
Curriculum Module for Elementary Grades 2-3
Grades 2-3 CurriCulum module for elementary Grades 2-3 UBEATS ModUlE 2/3 (1) https://sites.google.com/a/uncg.edu/ubeats/home Table of Contents Physical Science page 1: How does sound travel? 3 2: What are pitch and frequency? 7 3: How is sound affected by different mediums? 11 Life Science 1: How do we hear? 17 2: Can we determine how well other animals hear? 21 3: Do animals make music? 25 4: How does nature inspire human music making? 29 5: How can we describe animal sounds? 31 6: How do birds produce sounds? 35 7: What is the value of a signature sound? 39 8: How do animals communicate using tools? 41 9: Why do birds sing? 45 10: Do animals copy sounds? 49 11: How can humans imitate the sounds of animals? 53 12: How do animals compete with man-made sounds? 57 13: How do animal songs influence human music? 61 14: Can you make a symphony of sounds? 65 UBEATS ModUlE 2/3 (2) https://sites.google.com/a/uncg.edu/ubeats/home Physical Science 1: HoW doES SoUnd TrAvEl? InTrodUCTIon: Sound travels through waves of energy. The length and speed of the waves affect the sound’s frequency and amplitude. Prior to this activity, students should understand that sound is a lEArnIng oUTCoMES: The learner will form of energy that travels in waves. Sound energy is most readily explain how sound travels. The learner recognized by the human senses in the form of vibrations. Vibrations will be able to describe how frequency can be thought of the as the end result of the energy of sound and amplitude of sound are depicted in traveling through matter in waves. -
Supporting Information
Supporting Information Campbell et al. 10.1073/pnas.1421386112 SI Materials and Methods transformed into Escherichia coli JM109 High Efficiency Com- Genome Sequencing. The following amount of data were generated petent Cells. Transformed cells were grown in 3 mL of LB broth at for each sequencing technology: 136,081,956 pairs of 100 × 2 37 °C overnight, and plasmids were purified with E.Z.N.A. plas- short insert Illumina HiSeq reads for about 27 Gb total; 50,884,070 mid DNA mini kit I. The purified plasmids were used as PCR pairs of 100 × 2 large insert HiSeq reads for about 10 Gb total; templates to for further amplification of the probe region. The and 259,593 reads averaging 1600 nt for about 421 Mb total of amplified probes were subject to nick translation (>175 ng/μL PacBio data. DNA, 1× nick-translation buffer, 0.25 mM unlabeled dNTPs, 50 μM labeled dNTPs, 2.3 U/μL DNA polymerase I, 9 mU/μL Genome Annotation. Annotation of Hodgkinia DNA was done Dnase), using either Cy3 (MAGTRE006 and MAGTRE005), or using the phmmer module of HMMER v3.1b1 (1). All ORFs Cy5 (MAGTRE001 and MAGTRE012), and size selected for beginning with a start codon that overlapped a phmmer hit sizes in the range of 100–500 bp using Ampure XP beads. Probes were searched against a database of all Hodgkinia genes using with at least seven incorporated labeled dNTPs per 1,000 nucle- BLASTX 2.2.28+. MAGTRE Hodgkinia genes were considered otides as determined by spectroscopy were used for hybridization.