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Microsatellite Loci Isolated from the Mediterranean Species Cicada Barbara (Stål) and C
Molecular Ecology Notes (2002) 2, 173–175 PRIMERBlackwell Science, Ltd NOTE Microsatellite loci isolated from the Mediterranean species Cicada barbara (Stål) and C. orni L. (Hemiptera, Cicadoidea) S. G. SEABRA,*† H. R. WILCOCK,* J. A. QUARTAU† and M. W. BRUFORD* *School of Biosciences, Cardiff University, Main Building, Park Place, Cardiff, CF10 3TL, UK, †Centro de Biologia Ambiental e Departamento de Zoologia e Antropologia, Bloco C2, 3° Piso, Faculdade de Ciências de Lisboa, Campo Grande 1700 Lisboa, Portugal Abstract We describe the isolation of six polymorphic microsatellites for Cicada barbara (Stål), four of which are also polymorphic for the closely related Cicada orni L. Cicadas from several sites in the Iberian Peninsula, North Africa (C. barbara) and Greece (C. orni) were genotyped at these loci. Polymorphism is higher than that previously obtained with allozymes for these species. One locus allows species diagnosis (nonoverlapping allele size ranges) between C. barbara and C. orni and the others have some exclusive alleles for each species. Keywords: cicadas, Cicada barbara, Cicada orni, insects, microsatellites Received 6 November 2001; revision received 21 December 2001; accepted 21 December 2001 The genus Cicada L. (Hemiptera, Cicadoidea) includes agarose gel by electroelution into dialysis tubing and some sibling species that are morphologically very similar purified using Centricon Microconcentrators (Amicon). but distinguishable by the specific calling songs produced The fragments were enriched for CA and GA repeats using by males for mate recognition. Cicada barbara and C. orni are biotin-labelled probes and then ligated into a pUC18 vector two of these species that exist in sympatry in some areas (Amersham Pharmacia Biotech) (Hammond et al. -
Insects That Glow and Sing
IInsectsnsects ThatThat GGlowlow aandnd SSinging 6 Lesson Objectives Core Content Objectives Students will: Classify and identify insects as small six-legged animals with three body parts Identify and describe the three body parts of insects: head, thorax, and abdomen Identify the placement and/or purpose of an insect’s body parts Describe an insect’s exoskeleton Compare and contrast grasshoppers and crickets Language Arts Objectives The following language arts objectives are addressed in this lesson. Objectives aligning with the Common Core State Standards are noted with the corresponding standard in parentheses. Refer to the Alignment Chart for additional standards addressed in all lessons in this domain. Students will: Plan, draft, and edit an informative text that presents information about insects, including an introduction to a topic, relevant facts, and a conclusion (W.2.2) Participate in a shared research project on insects (W.2.7) With assistance, categorize and organize facts and information from “Insects That Glow and Sing” (W.2.8) Generate questions and gather information from multiple sources to answer questions about insects (W.2.8) Add drawings to descriptions of f ref ies, grasshoppers, and crickets to clarify ideas, thoughts, and feelings (SL.2.5) 82 Insects 6 | Insects That Glow and Sing © 2013 Core Knowledge Foundation Use the antonyms transparent and opaque appropriately in oral language (L.2.5a) Prior to listening to “Insects That Glow and Sing,” identify orally what they know and have learned about insects Use adverbs correctly in oral language Core Vocabulary bioluminescence, n. Light given off by some plants and animals, such as f ref ies, caused by a biochemical reaction Example: The night sky was f lled with the bioluminescence of dancing f ref ies. -
Teachers Resources
TEACHERS RESOURCES 1 CICADA BY SHAUN TAN Teachers Resources by Robyn Sheahan-Bright Introduction 4 Before and After Reading the Picture Book 5 Themes 5 Curriculum Topics 8 Study of History, Society and Environment English Language and Literacy Visual Literacy Creative Arts Learning Technologies Further Extension Activities 14 Further Topics for Discussion and Research 15 Conclusion 15 2 Author/Illustrator’s Inspiration 15 About the Author/Illustrator 19 Activity Sheets 21 Bibliography 24 About the Author of the Notes 26 3 INTRODUCTION Cicada tell story. Story good. Story simple. Story even human can understand. Tok Tok Tok! Back Cover Text Cicada has worked for the company for seventeen years – always finishes work perfectly; does unpaid overtime; is never offered promotion; has no access to office bathroom; sleeps in office wallspace; humans don’t like cicada; told to retire; climbs to top of building and ... This stunning open-ended text is a philosophical exploration of the culture of work but also of society. It traverses themes such as belonging, alien- ation, corporate bureaucracy and work, difference and prejudice, sub- mission to control/freedom, transformation/metamorphosis, resurrection and regeneration. Shaun Tan’s publisher describes the book as: ‘A dream of escape, a com- mentary on corporate slavery, a multi-layered allegory—Shaun has taken the humble cicada and created a mythic fairytale of magic, menace and wonder.’ Justin Ratcliffe, co-managing Director, Hachette B&P 15 November 2017 Shaun Tan is partly concerned here with Kafka’s nightmare of bureaucra- cy which, like many other concepts swirls together in a tantalising soup of ideas. -
Ethics, Edible Insects and Sustainable Food Choice in Schools Verity Jones* University of the West of England, Bristol, UK
British Educational Research Journal Vol. 46, No. 4, August 2020, pp. 894–908 DOI: 10.1002/berj.3655 ‘Just don’t tell them what’s in it’: Ethics, edible insects and sustainable food choice in schools Verity Jones* University of the West of England, Bristol, UK Supporting young people with global crises mitigation strategies is essential, yet loaded with ethical dilemmas for the educator. This study explores whether young people will make ethical decisions regarding the sustainability of food choice in schools, and based on the processes identified, what educators’ needs are in supporting transformative learning. This study is the first of its kind, where young people under the age of 14 have been tasting edible insects and discussing their role in a more sustainable diet. The article draws on mixed-method research with over 180 young people and their teachers in three schools in Wales and examines responses to a possible introduction of edible insects into school canteens. Highlighted is the complexity of sustainable food choices—likely to be identifiable with other young people and educators in western countries. The article considers how educators and policy makers may need to frame routes to positive sustainable action and the associ- ated impacts these may have on personal, social, political and environmental spheres. Keywords: edible insects; ethics; pedagogy; sustainability Introduction It is estimated that half of the planet’s surface considered habitable to plants is now being used for agriculture. Sarilo (2018) notes that 45% of this is being used for food that goes directly to humans, while a further 33% is for food to feed animals that will be slaughtered for human consumption. -
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 -
Rapid and Simple Species Identification of Cicada Exuviae
insects Article Rapid and Simple Species Identification of Cicada Exuviae Using COI-Based SCAR Assay Pureum Noh, Wook Jin Kim, Jun-Ho Song , Inkyu Park , Goya Choi and Byeong Cheol Moon * Herbal Medicine Resources Research Center, Korea Institute of Oriental Medicine, Naju 58245, Korea; [email protected] (P.N.); [email protected] (W.J.K.); [email protected] (J.-H.S.); [email protected] (I.P.); [email protected] (G.C.) * Correspondence: [email protected]; Tel.: +82-61-338-7100 Received: 5 February 2020; Accepted: 4 March 2020; Published: 6 March 2020 Abstract: Cicadidae periostracum (CP), the medicinal name of cicada exuviae, is well-known insect-derived traditional medicine with various pharmacological effects, e.g., anticonvulsive, anti-inflammatory, antitussive, and anticancer effects; it is also beneficial for the treatment of Parkinson’s disease. For appropriate CP application, accurate species identification is essential. The Korean pharmacopoeia and the pharmacopoeia of the People’s Republic of China define Cryptotympana atrata as the only authentic source of CP. Species identification of commercially distributed CP based on morphological features, however, is difficult because of the combined packaging of many cicada exuviae in markets, damage during distribution, and processing into powder form. DNA-based molecular markers are an excellent alternative to morphological detection. In this study, the mitochondrial cytochrome c oxidase subunit I sequences of C. atrata, Meimuna opalifera, Platypleura kaempferi, and Hyalessa maculaticollis were analyzed. On the basis of sequence alignments, we developed sequence-characterized amplified-region (SCAR) markers for efficient species identification. These markers successfully discriminated C. -
A New Neotibicen Cicada Subspecies (Hemiptera: Cicadidae)
Zootaxa 4272 (4): 529–550 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2017 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4272.4.3 http://zoobank.org/urn:lsid:zoobank.org:pub:C6234E29-8808-44DF-AD15-07E82B398D66 A new Neotibicen cicada subspecies (Hemiptera: Cicadidae) from the southeast- ern USA forms hybrid zones with a widespread relative despite a divergent male calling song DAVID C. MARSHALL1 & KATHY B. R. HILL Dept. of Ecology and Evolutionary Biology, University of Connecticut, 75 N. Eagleville Rd., Storrs, CT 06269 USA 1Corresponding author. E-mail: [email protected] Abstract A morphologically cryptic subspecies of Neotibicen similaris (Smith and Grossbeck) is described from forests of the Apalachicola region of the southeastern United States. Although the new form exhibits a highly distinctive male calling song, it hybridizes extensively where it meets populations of the nominate subspecies in parapatry, by which it is nearly surrounded. This is the first reported example of hybridization between North American nonperiodical cicadas. Acoustic and morphological characters are added to the original description of the nominate subspecies, and illustrations of com- plex hybrid song phenotypes are presented. The biogeography of N. similaris is discussed in light of historical changes in forest composition on the southeastern Coastal Plain. Key words: Acoustic behavior, sexual signals, hybridization, hybrid zone, parapatric distribution, speciation Introduction The cryptotympanine cicadas of North America have received much recent attention with the publication of comprehensive molecular and cladistic phylogenies and the reassignment of all former North American Tibicen Latreille species into new genera (Hill et al. -
Periodical Cicadas SP 341 3/21 21-0190 Programs in Agriculture and Natural Resources, 4-H Youth Development, Family and Consumer Sciences, and Resource Development
SP 341 Periodical Cicadas Frank A. Hale, Professor Originally developed by Harry Williams, former Professor Emeritus and Jaime Yanes Jr., former Assistant Professor Department of Entomology and Plant Pathology The periodical cicada, Magicicada species, has the broods have been described by scientists and are longest developmental period of any insect in North designated by Roman numerals. There are three 13-year America. There is probably no insect that attracts as cicada broods (XIX, XXII and XXIII) and 12 17-year much attention in eastern North America as does the cicada broods (I-X, XIII, and XIV). Also, there are three periodical cicada. Their sudden springtime emergence, distinct species of 17-year cicadas (M. septendecim, filling the air with their high-pitched, shrill-sounding M. cassini, and M. septendecula) and three species of songs, excites much curiosity. 13-year cicadas (M. tredecim, M. tredecassini, and M. tredecula). Two races of the periodical cicada exist. One race has a life cycle of 13 years and is common in the southeastern In Tennessee, Brood XIX of the 13-year cicada had a United States. The other race has a life cycle of 17 years spectacular emergence in 2011 (Map 1). In 2004 and and is generally more northern in distribution. Due 2021, Brood X of the 17-year cicada primarily emerged to Tennessee’s location, both the 13-year and 17-year in East Tennessee (Map 2). Brood X has the largest cicadas occur in the state. emergence of individuals for the 17-year cicada in the United States. Brood XXIII of the 13-year cicada last Although periodical cicadas have a 13- or 17-year cycle, emerged in West Tennessee in 2015 (Map 3). -
First Host Plant Record for Pacarina (Hemiptera, Cicadidae)
Neotropical Biology and Conservation 15(1): 77–88 (2020) doi: 10.3897/neotropical.15.e49013 SHORT COMMUNICATION First host plant record for Pacarina (Hemiptera, Cicadidae) Annette Aiello1, Brian J. Stucky2 1 Smithsonian Tropical Research Institute, Panama 2 Florida Museum of Natural History, University of Florida, Gainesville, FL, USA Corresponding author: Brian J. Stucky ([email protected]) Academic editor: P. Nunes-Silva | Received 4 December 2019 | Accepted 20 February 2020 | Published 19 March 2020 Citation: Aiello A, Stucky BJ (2020) First host plant record for Pacarina (Hemiptera, Cicadidae). Neotropical Biology and Conservation 15(1): 77–88. https://doi.org/10.3897/neotropical.15.e49013 Abstract Twenty-nine Pacarina (Hemiptera: Cicadidae) adults, 12 males and 17 females, emerged from the soil of a potted Dracaena trifasciata (Asparagaceae) in Arraiján, Republic of Panama, providing the first rearing records and the first definitive host plant records for any species of Pacarina. These reared Pacarina appear to be morphologically distinct from all known species of Pacarina and likely repre- sent an undescribed species. In light of this finding, we also discuss the taxonomy, biogeography, and ecology of Pacarina. Keywords cicada, Dracaena, host plant, rearing, taxonomy Introduction As far as is known, all cicadas are herbivores that spend the vast majority of their long life cycles as nymphs, living deep underground and feeding on the xylem sap of plant roots (Beamer 1928; Cheung and Marshall 1973; White and Strehl 1978). Be- cause of their relative inaccessibility to researchers, very little information is availa- ble about the host plant associations of juvenile cicadas. Consequently, even though adult cicadas are among the most conspicuous and familiar of all insects, the host plants of most cicada species’ nymphs remain unknown. -
New Combinations for Six Species Belonging to Cryptotympanini Handlirsch (Hemiptera: Cicadidae), Former Members of the Genus Tibicen Latreille, 1825
Zootaxa 4027 (2): 447–450 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Correspondence ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.4027.3.9 http://zoobank.org/urn:lsid:zoobank.org:pub:2C08AA8A-8FBB-4291-9A29-63CEB7BD77BA New combinations for six species belonging to Cryptotympanini Handlirsch (Hemiptera: Cicadidae), former members of the genus Tibicen Latreille, 1825 ALLEN F. SANBORN Department of Biology, Barry University, 11300 NE Second Avenue, Miami Shores, FL 33161-6695, USA. E-mail: [email protected] Abstract. The generic status of several species formerly placed in the genus Tibicen is reconsidered based on the recent erection of new genera as well as historical evidence. Subsolanus Moulds, 2015 syn. nov. is shown to be a junior synonym of Auritibicen Lee, 2015. Six species are reassigned from Tibicen to appropriate genera based on morphological characteristics. The genus Tibicen Latreille, 1825 has had a confusing past (see summary in Boulard & Puissant, 2014; Marshall & Hill, 2014; Sanborn, 2014a). A major factor in the confusion was the use of different species as the type species of the genus in Latreille (1825) (Cicada plebeja Scopoli, 1763) and Latreille (1829) (Cicada haematodes Scopoli, 1763), species that are currently classified in different subfamilies. This combined with the limited original descriptions led to confusion as to what taxa should be assigned to the genus. As a result, Tibicen became a convenient place to assign species when it was not known where else the species should be placed and species from all three of the current subfamilies were at one time or another classified in the genus Tibicen. -
Cicada Ovipositors Enhanced with Metals and Other Inorganic Elements Matthew S
www.nature.com/scientificreports OPEN An augmented wood-penetrating structure: Cicada ovipositors enhanced with metals and other inorganic elements Matthew S. Lehnert1*, Kristen E. Reiter1,2, Gregory A. Smith1 & Gene Kritsky3 Few insect species are as popular as periodical cicadas (Magicicada spp.). Despite representing an enormous biomass and numbers that exceed 370/m2 during mass emergences, the extended time period of the underground nymphal stages (up to 17 years) complicates investigations of their life history traits and ecology. Upon emergence, female cicadas mate and then use their ovipositors to cut through wood to lay their eggs. Given the ability to penetrate into wood, we hypothesized that the ovipositor cuticle is augmented with inorganic elements, which could increase hardness and reduce ovipositor fracturing. We used scanning electron microscopy and energy dispersive x-ray spectroscopy to evaluate the material properties of ovipositors of four cicada species, including three species of periodical cicadas. We found 14 inorganic elements of the cuticle, of which P, Ca, Si, Mg, Na, Fe, Zn, Mn, Cl, K, and S show the highest concentrations (%wt) near the apex of the ovipositor, where other structural modifcations for penetrating wood are present. To the best of our knowledge, this is the frst report of metal deposits in the cuticle of true bugs (Hemiptera, >80,000 described species). Te independent origin of traits that perform similar functions represents a cornerstone of natural selection. Examples of such convergent evolution can be found across animal taxa: intelligence among birds and apes1, echolocation among bats and dolphins2, and fuid-feeding mechanisms among fies and butterfies3. -
An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant.