Bumelia Webworm Urodus Parvula (Edwards 1881) (Insecta: Lepidoptera: Urodidae)1 Donald W
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SYSTEMATICS of the MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of T
SYSTEMATICS OF THE MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of the Requirements for The Degree of Doctor of Philosophy in the Graduate School of The Ohio State University By Sibyl Rae Bucheli, M.S. ***** The Ohio State University 2005 Dissertation Committee: Approved by Dr. John W. Wenzel, Advisor Dr. Daniel Herms Dr. Hans Klompen _________________________________ Dr. Steven C. Passoa Advisor Graduate Program in Entomology ABSTRACT The phylogenetics, systematics, taxonomy, and biology of Gelechioidea (Insecta: Lepidoptera) are investigated. This superfamily is probably the second largest in all of Lepidoptera, and it remains one of the least well known. Taxonomy of Gelechioidea has been unstable historically, and definitions vary at the family and subfamily levels. In Chapters Two and Three, I review the taxonomy of Gelechioidea and characters that have been important, with attention to what characters or terms were used by different authors. I revise the coding of characters that are already in the literature, and provide new data as well. Chapter Four provides the first phylogenetic analysis of Gelechioidea to include molecular data. I combine novel DNA sequence data from Cytochrome oxidase I and II with morphological matrices for exemplar species. The results challenge current concepts of Gelechioidea, suggesting that traditional morphological characters that have united taxa may not be homologous structures and are in need of further investigation. Resolution of this problem will require more detailed analysis and more thorough characterization of certain lineages. To begin this task, I conduct in Chapter Five an in- depth study of morphological evolution, host-plant selection, and geographical distribution of a medium-sized genus Depressaria Haworth (Depressariinae), larvae of ii which generally feed on plants in the families Asteraceae and Apiaceae. -
New Records of Microlepidoptera in Alberta, Canada
Volume 59 2005 Number 2 Journal of the Lepidopterists’ Society 59(2), 2005, 61-82 NEW RECORDS OF MICROLEPIDOPTERA IN ALBERTA, CANADA GREGORY R. POHL Natural Resources Canada, Canadian Forest Service, Northern Forestry Centre, 5320 - 122 St., Edmonton, Alberta, Canada T6H 3S5 email: [email protected] CHARLES D. BIRD Box 22, Erskine, Alberta, Canada T0C 1G0 email: [email protected] JEAN-FRANÇOIS LANDRY Agriculture & Agri-Food Canada, 960 Carling Ave, Ottawa, Ontario, Canada K1A 0C6 email: [email protected] AND GARY G. ANWEILER E.H. Strickland Entomology Museum, University of Alberta, Edmonton, Alberta, Canada, T6G 2H1 email: [email protected] ABSTRACT. Fifty-seven species of microlepidoptera are reported as new for the Province of Alberta, based primarily on speci- mens in the Northern Forestry Research Collection of the Canadian Forest Service, the University of Alberta Strickland Museum, the Canadian National Collection of Insects, Arachnids, and Nematodes, and the personal collections of the first two authors. These new records are in the families Eriocraniidae, Prodoxidae, Tineidae, Psychidae, Gracillariidae, Ypsolophidae, Plutellidae, Acrolepi- idae, Glyphipterigidae, Elachistidae, Glyphidoceridae, Coleophoridae, Gelechiidae, Xyloryctidae, Sesiidae, Tortricidae, Schrecken- steiniidae, Epermeniidae, Pyralidae, and Crambidae. These records represent the first published report of the families Eriocrani- idae and Glyphidoceridae in Alberta, of Acrolepiidae in western Canada, and of Schreckensteiniidae in Canada. Tetragma gei, Tegeticula -
Bionomics of Bagworms (Lepidoptera: Psychidae)
ANRV363-EN54-11 ARI 27 August 2008 20:44 V I E E W R S I E N C N A D V A Bionomics of Bagworms ∗ (Lepidoptera: Psychidae) Marc Rhainds,1 Donald R. Davis,2 and Peter W. Price3 1Department of Entomology, Purdue University, West Lafayette, Indiana, 47901; email: [email protected] 2Department of Entomology, Smithsonian Institution, Washington D.C., 20013-7012; email: [email protected] 3Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, 86011-5640; email: [email protected] Annu. Rev. Entomol. 2009. 54:209–26 Key Words The Annual Review of Entomology is online at bottom-up effects, flightlessness, mating failure, parthenogeny, ento.annualreviews.org phylogenetic constraint hypothesis, protogyny This article’s doi: 10.1146/annurev.ento.54.110807.090448 Abstract Copyright c 2009 by Annual Reviews. The bagworm family (Lepidoptera: Psychidae) includes approximately All rights reserved 1000 species, all of which complete larval development within a self- 0066-4170/09/0107-0209$20.00 enclosing bag. The family is remarkable in that female aptery occurs in ∗The U.S. Government has the right to retain a over half of the known species and within 9 of the 10 currently recog- nonexclusive, royalty-free license in and to any nized subfamilies. In the more derived subfamilies, several life-history copyright covering this paper. traits are associated with eruptive population dynamics, e.g., neoteny of females, high fecundity, dispersal on silken threads, and high level of polyphagy. Other salient features shared by many species include a short embryonic period, developmental synchrony, sexual segrega- tion of pupation sites, short longevity of adults, male-biased sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case. -
Attachment File.Pdf
Proc. Proc. Ar thropod. Embryo l. Soc. Jpn. 41 , 1-9 (2006) l (jJ (jJ 2006 Ar thropodan Embryological Society of Japan ISSN ISSN 1341-1527 [REVIEW] Character Phylogeny in Lepidopteran Embryogenesis: It s Revaluation and Issues to Be Resolved * Yukimasa KOBAYASHI Departme 四t 01 Biological Science , Graduate School 01 Sciences and Engineerin g, Tokyo Metropolitan University , Minami-ohsawa Minami-ohsawa 1-1 ,Hachioji , Tokyo 192-039 7, J4 μn E-mail: E-mail: [email protected] 1. 1. Introduction The order Lepidoptera is the insect group whose embryogenesis has been well investigated. Until about 30 years ago ,however , the materials had concentrated on the highest group of this order , or the former suborder Ditrysia , and nothing nothing had been known of the embryogenesis of primitive ,non-ditrysian Lepidoptera. In several ditrysian species , for example , Orgyia antiqua , Chilo suppressalis ,Pieris rapae , and Epiphyas pωtvittana ,it had been known that their embryonic embryonic membranes (serosa and amnion) are formed independentl y, not by the fusion of amnioserosal folds to be described described later ,and their germ bands or embryos grow in the submerged condition under the yolk until just before hatching hatching irrespective of the shape and size of eggs (Christensen , 1943; Okada , 1960; Tanaka , 1968; Anderson and Wood ,1968). Since such developmental processes are not common to other insects ,it had been speculated that these processes processes are characteristic not only of the Ditrysia but also of the whole Lepidoptera until the time when Ando and Tanaka Tanaka (1976 , 1980) found out a di 妊erent mode of ea r1 y embryogen 巴sis in the hepialid moths ,Endoclita , belonging to the the non-ditrysian Lepidoptera. -
Laajan Lajinsisäisen DNA-Viivakoodimuuntelun Esiintyvyys Ja Syyt Perhosilla Jonna Autto
Laajan lajinsisäisen DNA-viivakoodimuuntelun esiintyvyys ja syyt perhosilla Jonna Autto PRO GRADU-TUTKIELMA OULUN YLIOPISTO BIOLOGIAN TUTKINTO-OHJELMA KEVÄT 2018 Sisällysluettelo 1. Johdanto .................................................................................................................................................. 4 1.2. DNA-viivakoodit lajintunnistuksessa ja -rajaamisessa ......................................................................... 5 1.3. DNA-viivakoodaukseen liittyvät ongelmat........................................................................................ 10 1.3.1. Laaja lajinsisäinen DNA-viivakoodimuuntelu ............................................................................. 12 1.4. Perhoset .......................................................................................................................................... 18 1.5. Tutkimuksen tavoitteet ................................................................................................................... 19 2. Aineisto ja menetelmät .......................................................................................................................... 20 2.1. Aineiston kokoaminen ..................................................................................................................... 20 2.2. DNA:n eristys ja sekvensointi ........................................................................................................... 23 2.3. Analyysit ......................................................................................................................................... -
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. -
Ecology and Evolutionary Biology
Ecology and evolutionary biology SPRING/SUMMER NEWSLETTER 2019 NUMBER 34 CARL SCHLICHTING RETURNS TO FULL TIME TEACHING AND RESEARCH On June 30, 2019 Dr. Carl Schlichting returned to full time teaching and research responsibilities after serving as EEB’s Department Head for 5 1/2 years (2014-2019). Carl received his B.S. in Zoology from Ohio State University, M.A. in Ecology and Evolution from SUNY at Stony Brook, and a Ph.D. in Botany from the University of Texas (Austin). Carl joined the EEB Department in 1988 as Assistant Professor at the Hartford campus. In 2000 he was promoted to Professor and joined the faculty in Storrs in 2002. He is looking forward to finishing some manuscripts and analyzing some old (Phox and Lobelia) and new (Pelargonium) datasets that have been awaiting his attention! During Carl’s tenure as Head, EEB welcomed eight new faculty members, six at Storrs and one each at Hartford and Stamford. Although he takes little credit, he notes that Department grant expenditures have risen by 40% to $3.5M/ year, and the number of EEB majors has risen from 55 to 80. Carl performed day-to-day management of the multi- year planning process for EEB’s eventual move into a newly renovated Gant Building, as well as the negotiations for a new Greenhouse facility. He will continue to manage the planning and move into EEB’s new Gant space. The exact dates of the two-phase moves will be announced in an upcoming newsletter so stay tuned. Faculty, students and staff are grateful to Carl for his leadership and support during his tenure as Department Head. -
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. -
Interesting Early Stages of Some Sri Lankan Moths Typical Moth Life Cycle
Interesting early stages of some Sri Lankan Moths Typical Moth Life Cycle A Cocoon is a casing of spun silk produced by many insects to form a protective covering for the Pupa. Many Moth Caterpillars for example produce silk cocoons. Cocoons can be of various types, from hard to soft, with various colours dependent on the species involved. Wingless Females Some female moths of the Subfamily Lymantriinae are flightless. Male Female Orgyia sp. Lymantria sp. Life Cycle of Lymantria ampla Life cycle of Fir tussock moth (Orgyia detrita) Ant-mimic Moth caterpillars • Caterpillars in the moth genus, Homodes Guenée have been documented to be closely associated with weaver ants, as well as resembling them in terms of morphology and behaviour (Shelford, 1902, 1916; Kalshoven, 1961; Common, 1990; Holloway, 2005). In Sri Lanka, at least three species have been previously recorded • Homodes fulva • Homodes crocea Homodes crocea • Homodes vivida Dorsal (a) and posterior (b) views of the raised rear end of the caterpillar, Lobster Moth (Stauropus alternus) • First instar larva is a very good ant mimic both in appearance and behaviour • Resting posture of its mid instar look like an irregularly curved, dead leaf. • This resemblance to dried or dead leaf debris is certainly applicable to the later instars as well. Bagworms (Psychidae) • The bagworm family (Lepidoptera: Psychidae) includes approximately 1000 species, all of which complete larval development within a self enclosing bag. • In Sri Lanka 23 species have been recorded in this family • Some bagworms are specialized in their host plants (monophagous) , while others can feed on a variety of plant species (polyphagous) Eumeta variegata • A bagworm begins to build its case as soon as it hatches. -
ABHANDLUNGEN Aus Dem Westfälischen Museum Für Naturkunde - Landschaftsverband Westfalen-Lippe
ISS N 0023 - 7906 ABHANDLUNGEN aus dem Westfälischen Museum für Naturkunde - Landschaftsverband Westfalen-Lippe - herausgegeben von P r o f. D r. L. F R A N Z I S K E T Direktor des Westfälischen Museums für Naturkunde, Münster 44. JAHRGANG 1982, HEFT 1 Lepidoptera Westfalica HANS-JOACHIM WEIGT, Unna Westfälische Ve r eindruckerei 4 4 00 Münster Die Abhandlungen aus dem Westfälischen Museum für Naturkunde bringen wi ssenschaftliche Beiträge zur Erforschung des Naturraumes Westfalen. Die Autoren werden gebeten, die Manuskripte in Maschinenschrift (1 112 Zeilen Abstand) druckfertig einzusenden an: Westfälisches Museum für Naturkunde Schriftleitung Abhandlungen, Dr. Brunhild Gries Sentruper Straße 285, 4400 MÜNSTER Lateinische Art- und Rassennamen sind fü r den Kursivdruck mit einer Wellen linie zu unterschlängeln; Wörter, di e in Sperrdruck hervorgehoben werden sollen, sind m it Bleistift mit ei ner unterbrochenen Linie zu unterstreichen. Autorennamen sind in Großbuchstaben zu schreiben. Abschnitte, die in Kl eindruck gebracht wer den kö nnen, sind am linken Rand mit „petit" zu bezeichnen. Abbildungen (Karten, Zeichnungen, Fotos) sollen ni cht direkt, sondern auf einem transparenten mit einem Falz angeklebten Deckblatt beschriftet werden. Unsere Grafikerin über• trägt Ihre Vorlage in das Original. Abbildungen werden nur aufgenommen, wenn sie bei Verkleinerung auf Satzspiegelbreite (12 ,5 cm) noch gut lesbar sind. Die Herstellung größerer Abbildungen kann wegen der Kosten nur in solchen Fällen erfolgen, in denen grafische Darstellungen einen entscheidenden Beitrag der Arbeit ausmachen. Das Literaturverzeichnis ist nach folgendem Muster anzufertigen: BUDDE, H. & W. BROCKHAUS (1954): Die Vegetation des westfälischen Berglandes. - Decheniana 102, 47-275. KRAMER, H. (1962): Zum Vorkom men des Fischreihers in der Bundesrepublik Deutschland. -
Lepidoptera Checklist Cr1a
Seznam motýlů České republiky Checklist of Lepidoptera of the Czech Republic (Insecta: Lepidoptera) Zdeněk Laštůvka* & Jan Liška** *Ústav zoologie, rybářství, hydrobiologie a včelařství AF MZLU v Brně Department of Zoology, Fisheries, Hydrobiology and Apiculture, Mendel University of Agriculture and Forestry in Brno **Výzkumný ústav lesního hospodářství a myslivosti Jíloviště-Strnady Forestry and Game Management Research Institute Jíloviště-Strnady 1 Úvodm Předložený seznam přináší aktuální přehled druhů motýlůČeské republiky. Zahrnuje druhy v současnosti nebo minulosti dlouhodobě přítomné, migranty, druhy s nestálým nebo nepravidelným výskytem i druhy synantropní. Ze seznamu jsou naopak vyloučeny druhy uváděné na základě chybného určení, druhy, jejichž výskyt není spolehlivě doložen a ojedinělé nálezy zavlečených jedinců cizích druhů bez následného vzniku trvalých populací. UUUSeznam vychází z katalogů motýlů Moravy a české části Slezka (Laštůvka, 1993) a Čech (Novák & Liška, 1997), resp. celé České republiky (Laštůvka, 1998), přičemž jsou zohledněny systematické a nomenklatorické změny, ke kterým od vydání těchto publikací došlo. V zájmu přesnějšího vymezení dosud známého rozšíření v České republice jsou označeny druhy, jejichž známý výskyt je omezen jen na území termofytika nebo oreofytika. UUUPoznámky k výskytu některých druhů doplnili a tím k co neúplnější podobě tohoto seznamu přispěli pánové V. Bělín, J. Bezděk, T. Dobrovský, M. Dvořák, G. Elsner, V. Elsner, A. Gottwald, F. Gregor, V. Hula, M. Janovský, J. Jaroš, T. Jirgl F. Kopeček, J. Korynta, T. Kuras, A. Laštůvka, J. Marek, L. Maršík, J. Němý, I. Novák, M. Petrů, P. Potocký, † D. Povolný, J. Procházka, J. Sitek, J. Skyva, V. Štolc, J. Šumpich, J. Uřičář, J. Vávra, V. Vrabec, M. Žemlička a další entomologové. K některým taxonomickým a nomenklatorickým problémům se laskavě vyjádřili J. -
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