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Modular Structure, Sequence Diversification and Appropriate
www.nature.com/scientificreports OPEN Modular structure, sequence diversifcation and appropriate nomenclature of seroins produced Received: 17 July 2018 Accepted: 14 February 2019 in the silk glands of Lepidoptera Published: xx xx xxxx Lucie Kucerova1, Michal Zurovec 1,2, Barbara Kludkiewicz1, Miluse Hradilova3, Hynek Strnad3 & Frantisek Sehnal1,2 Seroins are small lepidopteran silk proteins known to possess antimicrobial activities. Several seroin paralogs and isoforms were identifed in studied lepidopteran species and their classifcation required detailed phylogenetic analysis based on complete and verifed cDNA sequences. We sequenced silk gland-specifc cDNA libraries from ten species and identifed 52 novel seroin cDNAs. The results of this targeted research, combined with data retrieved from available databases, form a dataset representing the major clades of Lepidoptera. The analysis of deduced seroin proteins distinguished three seroin classes (sn1-sn3), which are composed of modules: A (includes the signal peptide), B (rich in charged amino acids) and C (highly variable linker containing proline). The similarities within and between the classes were 31–50% and 22.5–25%, respectively. All species express one, and in exceptional cases two, genes per class, and alternative splicing further enhances seroin diversity. Seroins occur in long versions with the full set of modules (AB1C1B2C2B3) and/or in short versions that lack parts or the entire B and C modules. The classes and the modular structure of seroins probably evolved prior to the split between Trichoptera and Lepidoptera. The diversity of seroins is refected in proposed nomenclature. Te silk spun by caterpillars is a composite material based on two protein agglomerates that have been known for centuries as fbroin and sericin. -
Acoustic Communication in the Nocturnal Lepidoptera
Chapter 6 Acoustic Communication in the Nocturnal Lepidoptera Michael D. Greenfield Abstract Pair formation in moths typically involves pheromones, but some pyra- loid and noctuoid species use sound in mating communication. The signals are generally ultrasound, broadcast by males, and function in courtship. Long-range advertisement songs also occur which exhibit high convergence with commu- nication in other acoustic species such as orthopterans and anurans. Tympanal hearing with sensitivity to ultrasound in the context of bat avoidance behavior is widespread in the Lepidoptera, and phylogenetic inference indicates that such perception preceded the evolution of song. This sequence suggests that male song originated via the sensory bias mechanism, but the trajectory by which ances- tral defensive behavior in females—negative responses to bat echolocation sig- nals—may have evolved toward positive responses to male song remains unclear. Analyses of various species offer some insight to this improbable transition, and to the general process by which signals may evolve via the sensory bias mechanism. 6.1 Introduction The acoustic world of Lepidoptera remained for humans largely unknown, and this for good reason: It takes place mostly in the middle- to high-ultrasound fre- quency range, well beyond our sensitivity range. Thus, the discovery and detailed study of acoustically communicating moths came about only with the use of electronic instruments sensitive to these sound frequencies. Such equipment was invented following the 1930s, and instruments that could be readily applied in the field were only available since the 1980s. But the application of such equipment M. D. Greenfield (*) Institut de recherche sur la biologie de l’insecte (IRBI), CNRS UMR 7261, Parc de Grandmont, Université François Rabelais de Tours, 37200 Tours, France e-mail: [email protected] B. -
Towards a Mitogenomic Phylogeny of Lepidoptera ⇑ Martijn J.T.N
Molecular Phylogenetics and Evolution 79 (2014) 169–178 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Towards a mitogenomic phylogeny of Lepidoptera ⇑ Martijn J.T.N. Timmermans a,b, , David C. Lees c, Thomas J. Simonsen a a Department of Life Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom b Department of Life Sciences, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom c Department of Zoology, Cambridge University, Downing Street CB2 3EJ, United Kingdom article info abstract Article history: The backbone phylogeny of Lepidoptera remains unresolved, despite strenuous recent morphological and Received 13 January 2014 molecular efforts. Molecular studies have focused on nuclear protein coding genes, sometimes adding a Revised 11 May 2014 single mitochondrial gene. Recent advances in sequencing technology have, however, made acquisition of Accepted 26 May 2014 entire mitochondrial genomes both practical and economically viable. Prior phylogenetic studies utilised Available online 6 June 2014 just eight of 43 currently recognised lepidopteran superfamilies. Here, we add 23 full and six partial mitochondrial genomes (comprising 22 superfamilies of which 16 are newly represented) to those Keywords: publically available for a total of 24 superfamilies and ask whether such a sample can resolve deeper tRNA rearrangement lepidopteran phylogeny. Using recoded datasets we obtain topologies that are highly congruent with Ditrysia Illumina prior nuclear and/or morphological studies. Our study shows support for an expanded Obtectomera LR-PCR including Gelechioidea, Thyridoidea, plume moths (Alucitoidea and Pterophoroidea; possibly along with Pooled mitochondrial genome assembly Epermenioidea), Papilionoidea, Pyraloidea, Mimallonoidea and Macroheterocera. -
Phylogeny and Evolution of Lepidoptera
EN62CH15-Mitter ARI 5 November 2016 12:1 I Review in Advance first posted online V E W E on November 16, 2016. (Changes may R S still occur before final publication online and in print.) I E N C N A D V A Phylogeny and Evolution of Lepidoptera Charles Mitter,1,∗ Donald R. Davis,2 and Michael P. Cummings3 1Department of Entomology, University of Maryland, College Park, Maryland 20742; email: [email protected] 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560 3Laboratory of Molecular Evolution, Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland 20742 Annu. Rev. Entomol. 2017. 62:265–83 Keywords Annu. Rev. Entomol. 2017.62. Downloaded from www.annualreviews.org The Annual Review of Entomology is online at Hexapoda, insect, systematics, classification, butterfly, moth, molecular ento.annualreviews.org systematics This article’s doi: Access provided by University of Maryland - College Park on 11/20/16. For personal use only. 10.1146/annurev-ento-031616-035125 Abstract Copyright c 2017 by Annual Reviews. Until recently, deep-level phylogeny in Lepidoptera, the largest single ra- All rights reserved diation of plant-feeding insects, was very poorly understood. Over the past ∗ Corresponding author two decades, building on a preceding era of morphological cladistic stud- ies, molecular data have yielded robust initial estimates of relationships both within and among the ∼43 superfamilies, with unsolved problems now yield- ing to much larger data sets from high-throughput sequencing. Here we summarize progress on lepidopteran phylogeny since 1975, emphasizing the superfamily level, and discuss some resulting advances in our understanding of lepidopteran evolution. -
Amphiesmeno- Ptera: the Caddisflies and Lepidoptera
CY501-C13[548-606].qxd 2/16/05 12:17 AM Page 548 quark11 27B:CY501:Chapters:Chapter-13: 13Amphiesmeno-Amphiesmenoptera: The ptera:Caddisflies The and Lepidoptera With very few exceptions the life histories of the orders Tri- from Old English traveling cadice men, who pinned bits of choptera (caddisflies)Caddisflies and Lepidoptera (moths and butter- cloth to their and coats to advertise their fabrics. A few species flies) are extremely different; the former have aquatic larvae, actually have terrestrial larvae, but even these are relegated to and the latter nearly always have terrestrial, plant-feeding wet leaf litter, so many defining features of the order concern caterpillars. Nonetheless, the close relationship of these two larval adaptations for an almost wholly aquatic lifestyle (Wig- orders hasLepidoptera essentially never been disputed and is supported gins, 1977, 1996). For example, larvae are apneustic (without by strong morphological (Kristensen, 1975, 1991), molecular spiracles) and respire through a thin, permeable cuticle, (Wheeler et al., 2001; Whiting, 2002), and paleontological evi- some of which have filamentous abdominal gills that are sim- dence. Synapomorphies linking these two orders include het- ple or intricately branched (Figure 13.3). Antennae and the erogametic females; a pair of glands on sternite V (found in tentorium of larvae are reduced, though functional signifi- Trichoptera and in basal moths); dense, long setae on the cance of these features is unknown. Larvae do not have pro- wing membrane (which are modified into scales in Lepi- legs on most abdominal segments, save for a pair of anal pro- doptera); forewing with the anal veins looping up to form a legs that have sclerotized hooks for anchoring the larva in its double “Y” configuration; larva with a fused hypopharynx case. -
Lepidoptera, Incurvariidae) with Two New Species from China and Japan
Zootaxa 4927 (2): 209–233 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2021 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4927.2.3 http://zoobank.org/urn:lsid:zoobank.org:pub:96B9981B-01B5-4828-A4C6-E2E4A08DB8F2 Review of the genus Vespina (Lepidoptera, Incurvariidae) with two new species from China and Japan TOSHIYA HIROWATARI1*, SADAHISA YAGI1, ISSEI OHSHIMA2, GUO-HUA HUANG3 & MIN WANG4 1Entomological laboratory, Faculty of Agriculture, Kyushu University, Fukuoka, 819-0395 Japan. �[email protected]; https://orcid.org/0000-0002-4261-1219 2Department of Life and Environmental Sciences, Kyoto Prefectural University, Kyoto, 606-8522 Japan. �[email protected]; https://orcid.org/0000-0001-8295-9749 3Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha 410128, Hunan, China. �[email protected]; https://orcid.org/0000-0002-6841-0095 4Department of Entomology, South China Agricultural University, Guangzhou 510640, Guangdong, China. �[email protected]; https://orcid.org/0000-0001-5834-4058 *Corresponding author. �[email protected]; https://orcid.org/0000-0002-6839-2229 Abstract Asian species of the genus Vespina Davis, 1972 (Lepidoptera, Incurvariidae) are mainly reviewed. Vespina meridiana Hirowatari & Yagi sp. nov. from the Ryukyu Islands, Japan, and Vespina sichuana Hirowatari, Huang & Wang sp. nov. from Sichuan, China, are described. The previously known Vespina species are associated with plants from the Fagaceae family on the western coast of the USA and East Asia and with Sapindaceae (Aceraceae) in eastern Europe. -
Journal of the Lepidopterists' Society
124 JOURNAL OF THE LEPIDOPTERISTS' SOCIETY THE STATUS OF THE GLYPHIPTERIGIDAE AND A REASSESSMENT OF RELATIONSHIPS IN YPONOMEUTOID FAMILIES AND DITRYSIAN SUPERFAMILIESl JOHN B. HEPPNER2 Department of Entomology and Nematology, IFAS, University of Florida, Gainesville, Florida 32611 Current studies of the North American Glyphipterigidae have revealed major fundamental morphological and behavioral characters which dem onstrate that the inclusion of thc choreutid and glyphipterigid groups within a single family is untenable. The discordant characters involved have been shown in the past by other workers to be so fundamentally and evolutionarily conservative in Lepidoptera phylogeny that it is not even possible to consider the two groups to have evolved within the same superfamily, Glyphipterigid moths have long been considered of unusual interest because of apparent affinities to the Yponomeutidae and the Sesiidae, as well as to the Tortricidae. Most early workers considered them as dis tinct groups: the choreutids were placed with the tortricids and the glyphipterigids sensu stricto were placed among the tineoid moths. This segregation was rarely altered until Meyrick (1914) combined them into one family. Meyrick's classification was based largely on general facies-the two groups share a number of superficial characters-and not fundamental relationships. He also relied strongly on wing venation and did not use genitalia, internal morphology or larval characters. He formed a conglomeration of what now are no less than nine distinct families in several superfamilies, although he realized the true affinities of many of the included genera in later years. Current revisionary studies on the choreutids and glyphipterigids, using modern systematic tech niques, are revealing the true affinities of these moths. -
Checklist of Texas Lepidoptera Knudson & Bordelon, Jan 2018 Texas Lepidoptera Survey
1 Checklist of Texas Lepidoptera Knudson & Bordelon, Jan 2018 Texas Lepidoptera Survey ERIOCRANIOIDEA TISCHERIOIDEA ERIOCRANIIDAE TISCHERIIDAE Dyseriocrania griseocapitella (Wlsm.) Eriocraniella mediabulla Davis Coptotriche citripennella (Clem.) Eriocraniella platyptera Davis Coptotriche concolor (Zell.) Coptotriche purinosella (Cham.) Coptotriche clemensella (Cham). Coptotriche sulphurea (F&B) NEPTICULOIDEA Coptotriche zelleriella (Clem.) Tischeria quercitella Clem. NEPTICULIDAE Coptotriche malifoliella (Clem.) Coptotriche crataegifoliae (Braun) Ectoedemia platanella (Clem.) Coptotriche roseticola (F&B) Ectoedemia rubifoliella (Clem.) Coptotriche aenea (F&B) Ectoedemia ulmella (Braun) Asterotriche solidaginifoliella (Clem.) Ectoedemia obrutella (Zell.) Asterotriche heliopsisella (Cham.) Ectoedemia grandisella (Cham.) Asterotriche ambrosiaeella (Cham.) Nepticula macrocarpae Free. Asterotriche helianthi (F&B) Stigmella scintillans (Braun) Asterotriche heteroterae (F&B) Stigmella rhoifoliella (Braun) Asterotriche longeciliata (F&B) Stigmella rhamnicola (Braun) Asterotriche omissa (Braun) Stigmella villosella (Clem.) Asterotriche pulvella (Cham.) Stigmella apicialbella (Cham.) Stigmella populetorum (F&B) Stigmella saginella (Clem.) INCURVARIOIDEA Stigmella nigriverticella (Cham.) Stigmella flavipedella (Braun) PRODOXIDAE Stigmella ostryaefoliella (Clem.) Stigmella myricafoliella (Busck) Tegeticula yuccasella (Riley) Stigmella juglandifoliella (Clem.) Tegeticula baccatella Pellmyr Stigmella unifasciella (Cham.) Tegeticula carnerosanella Pellmyr -
Redalyc.New Records of Lepidoptera from the Iberian Peninsula for 2015
SHILAP Revista de Lepidopterología ISSN: 0300-5267 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España Lastuvka, A.; Lastuvka, Z. New records of Lepidoptera from the Iberian Peninsula for 2015 (Insecta: Lepidoptera) SHILAP Revista de Lepidopterología, vol. 43, núm. 172, diciembre, 2015, pp. 633-644 Sociedad Hispano-Luso-Americana de Lepidopterología Madrid, España Available in: http://www.redalyc.org/articulo.oa?id=45543699008 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative SHILAP Revta. lepid., 43 (172), diciembre 2015: 633-644 eISSN: 2340-4078 ISSN: 0300-5267 New records of Lepidoptera from the Iberian Peninsula for 2015 (Insecta: Lepidoptera) A. Lastuvka & Z. Lastuvka Abstract New records of Nepticulidae, Heliozelidae, Adelidae, Tischeriidae, Gracillariidae, Argyresthiidae, Lyonetiidae and Sesiidae for Portugal and Spain are presented. Stigmella minusculella (Herrich-Schäffer, 1855), S. tormentillella (Herrich-Schäffer, 1860), Parafomoria helianthemella (Herrich-Schäffer, 1860), Antispila metallella ([Denis & Schiffermüller], 1775), Nematopogon metaxella (Hübner, [1813]), Tischeria dodonaea Stainton, 1858, Coptotriche gaunacella (Duponchel, 1843), Caloptilia fidella (Reutti, 1853), Phyllonorycter monspessulanella (Fuchs, 1897), P. spinicolella (Zeller, 1846), Lyonetia prunifoliella -
Lepidoptera: Gracillariidae) in Turkey
DOI:http://dx.doi.org/10.16969/teb.16248 Türk. entomol. bült., 2016, 6(1): 9-14 ISSN 2146-975X Orijinal article (Original araştırma) A new host and natural enemies of Dialectica scalariella (Zeller) (Lepidoptera: Gracillariidae) in Turkey Dialectica scalariella (Zeller) (Lepidoptera: Gracillariidae)’nın yeni konukçu ve doğal düşmanları Cumali ÖZASLAN1* Halil BOLU1 Feza CAN CENGİZ2 Puja RAY3 Summary The study was carried out to determine leaf mining insects species feeding on Echium italicum L. (Boraginaceae) (Italian viper’s bugloss) growing in wheat fields of Edirne and Samsun provinces in 2013. As result of this study, Dialectica scalariella (Zeller, 1850) (Lepidoptera: Gracillariidae) adults were obtained from the samples collected from both provinces. D. scalariella is a first record for insect fauna of Edirne and Samsun provinces. In addition, parasitoids Apanteles sp. (Hymenoptera: Braconidae) and Sympiesis sp. (Hymenoptera: Eulophidae) were obtained from D. scalariella larvae collected from E. italicum in Edirne. Key words: Dialectica scalariella, Echium italicum, natural enemies, host plant, Turkey Özet Bu çalışma, Edirne ve Samsun illerinde buğday üretim alanlarında bulunan İtalyan engerek otu (Echium italicum L.) (Boraginaceae) ile beslenen galeri böceklerini belirlemek amacıyla 2013 yılında yürütülmüştür. Çalışma sonucunda Edirne ve Samsun illerinden toplanan örneklerden Dialectica scalariella (Zeller, 1850) (Lepidoptera: Gracillariidae)’nın erginleri elde edilmiştir. D. scalariella Edirne ve Samsun illeri böcek faunası için -
Beginner S Guide to Moths of the Midwest Geometers
0LGZHVW5HJLRQ86$ %HJLQQHU V*XLGHWR0RWKVRIWKH0LGZHVW*HRPHWHUV $QJHOOD0RRUHKRXVH ,OOLQRLV1DWXUH3UHVHUYH&RPPLVVLRQ Photos: Angella Moorehouse ([email protected]). Produced by: Angella Moorehouse with the assistance of Alicia Diaz, Field Museum. Identification assistance provided by: multiple sources (inaturalist.org; bugguide.net) )LHOG0XVHXP &&%<1&/LFHQVHGZRUNVDUHIUHHWRXVHVKDUHUHPL[ZLWKDWWULEXWLRQEXWFRPPHUFLDOXVHRIWKHRULJLQDOZRUN LVQRWSHUPLWWHG >ILHOGJXLGHVILHOGPXVHXPRUJ@>@YHUVLRQ $ERXWWKH%(*,11(5¶6027+62)7+(0,':(67*8,'(6 Most photos were taken in west-central and central Illinois; a fewDUH from eastern Iowa and north-central Wisconsin. Nearly all were posted to identification websites: BugGuide.netDQG iNaturalist.org. Identification help was provided by Aaron Hunt, Steve Nanz, John and Jane Balaban, Chris Grinter, Frank Hitchell, Jason Dombroskie, William H. Taft, Jim Wiker,DQGTerry Harrison as well as others contributing to the websites. Attempts were made to obtain expert verifications for all photos to the field identification level, however, there will be errors. Please contact the author with all corrections Additional assistance was provided by longtime Lepidoptera survey partner, Susan Hargrove. The intention of these guides is to provide the means to compare photographs of living specimens of related moths from the Midwest to aid the citizen scientists with identification in the field for Bio Blitz, Moth-ers Day, and other night lighting events. A taxonomic list to all the species featured is provided at the end along with some field identification tips. :(%6,7(63529,',1*,'(17,),&$7,21,1)250$7,21 BugGuide.net LNaturalist.org Mothphotographersgroup.msstate.edu Insectsofiowa.org centralillinoisinsects.org/weblog/resources/ :+,&+027+*8,'(7286( The moths were split into 6 groups for the purposes of creating smaller guides focusing on similar features of 1 or more superfamilies. -
BARAN T. on the New and Rare Microlepidoptera (Lepidoptera)
POLISH JOURNAL OF ENTOMOLOGY POLSKIE P I S M O ENTOMOLOGICZNE VOL. 77 : 133-143 Bydgoszcz 30 June 2008 On the new and rare Microlepidoptera (Lepidoptera) in Polish fauna TOMASZ BARAN Department of Invertebrate Zoology, University of Rzeszów, Cegielniana 12, 35-959 Rzeszów, Poland; e-mail: [email protected] ABSTRACT. For eighteen micro-moth species new distributional records are given. Dichomeris rasilella (HERRICH -SCHÄFFER , 1854) is for the first time reported from Poland. For Coleophora pulmonariella RAGONOT , 1874 the first reliable record is given. In addition, some diagnostic fea- tures of Dichomeris rasilella and Coleophora pulmonariella are also mentioned. In the paper, adult specimens of Argyresthia pulchella LIENIG & ZELLER , 1846, Chrysoclista splendida KARSHOLT , 1997, Coleophora pulmonariella , Coleophora onopordiella ZELLER , 1849, Dichomeris rasilella and Wockia asperipunctella (BRUAND , 1851), larval mines of Argyresthia thuiella (PACKARD , 1871) and Monochroa sepicolella (HERRICH -SCHÄFFER , 1854), as well as female genitalia, aedeagus and larval case of Coleophora pulmonariella are figured. KEY WORDS: Lepidoptera, Microlepidoptera, faunistics, new records, Poland. INTRODUCTION The latest comprehensive checklist of Polish Lepidoptera (BUSZKO & NOWACKI 2000) revealed among others that many regions of the country had not been sufficiently investi- gated in the past, as well as that many species, especially those of micro-moths had not been found again for even tens of years. Therefore, for a few years the author has been trying to fill this gap. In result of a recent field research, carried out predominantly in south eastern Poland in 2007, eighteen interesting records of Microlepidoptera have been found. In the article these faunistic data are presented. The seldom-collected moths treated here belong to the following families: Adelidae, Tineidae, Gracillariidae, Yponomeutidae, Elachistidae, Agonoxenidae, Scythrididae, Coleophoridae, Gelechiidae, Choreutidae, and Pterophoridae.