Supplementary Documentation on Phylogenetic Relations Used to Build the Working Tree
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Self-Repair and Self-Cleaning of the Lepidopteran Proboscis
Clemson University TigerPrints All Dissertations Dissertations 8-2019 Self-Repair and Self-Cleaning of the Lepidopteran Proboscis Suellen Floyd Pometto Clemson University, [email protected] Follow this and additional works at: https://tigerprints.clemson.edu/all_dissertations Recommended Citation Pometto, Suellen Floyd, "Self-Repair and Self-Cleaning of the Lepidopteran Proboscis" (2019). All Dissertations. 2452. https://tigerprints.clemson.edu/all_dissertations/2452 This Dissertation is brought to you for free and open access by the Dissertations at TigerPrints. It has been accepted for inclusion in All Dissertations by an authorized administrator of TigerPrints. For more information, please contact [email protected]. SELF-REPAIR AND SELF-CLEANING OF THE LEPIDOPTERAN PROBOSCIS A Dissertation Presented to the Graduate School of Clemson University In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy ENTOMOLOGY by Suellen Floyd Pometto August 2019 Accepted by: Dr. Peter H. Adler, Major Advisor and Committee Co-Chair Dr. Eric Benson, Committee Co-Chair Dr. Richard Blob Dr. Patrick Gerard i ABSTRACT The proboscis of butterflies and moths is a key innovation contributing to the high diversity of the order Lepidoptera. In addition to taking nectar from angiosperm sources, many species take up fluids from overripe or sound fruit, plant sap, animal dung, and moist soil. The proboscis is assembled after eclosion of the adult from the pupa by linking together two elongate galeae to form one tube with a single food canal. How do lepidopterans maintain the integrity and function of the proboscis while foraging from various substrates? The research questions included whether lepidopteran species are capable of total self- repair, how widespread the capability of self-repair is within the order, and whether the repaired proboscis is functional. -
Any Reader Who Knew the British Butterflies in The
VOLUME 50, NUMBER 2 ]53 Any reade r who knew the British butterflies in the 1950s and before will have memories of rich localities, of pastures, woods and downland from which once common species have long vanished, even if the land seems superficially to have survved. This book misses no opportunity for optimism, however: a few expanding ranges, of the Essex Skipper (Thymelicl1s lineola), the Speckled Wood (Pararge aegeria), and perhaps the White Admiral (Ladoga camilla), are recorded, together with current conservation efforts to keep now highly restricted and threatened species on the British l.'st. To read this book in conjunction with South or Frohawk reveals the general and rapid decline of a fauna, for long relatively stable, for which the blame lies almost entirely with habitat change and degradation, in their richly varied aspects. The illustrations, by Richard Lewington, have neve r, ill my vi.cw, been surpassed. Each butterfly is shown by an upperside (of both sexes where appreciably dimorphic) in "set" position, and by an underside in "perching" pose. British lepidopterists have for long paid much attention to aberrations, and many very remarkable examples of these variants are shown. Other figures, illustrating the butterflies at rest or nectaring are particularly striking through Lewington's use of black and white pencil for the plart or other perching site, against which the beauty of the painted butterflies is seen to best advantage. The effect achieved, for example, by a mating pair of Black Hairstreaks (Strymonidia pruni) on a penciled blackthorn twig, of a male Purple Hairstreak (Ql1ercl1sia quercus) basking on a an oak twig, or the once widespread but now endange red High Brown Fritillary (Argyrmis adippe) perching on a bramble, selected for the title page, is brilliant. -
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. -
Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI
The Great Lakes Entomologist Volume 35 Number 1 - Spring/Summer 2002 Number 1 - Article 10 Spring/Summer 2002 April 2002 Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI. Miscellaneous Small Families (Lepidoptera) Edward G. Voss University of Michigan Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Voss, Edward G. 2002. "Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), Michigan: VI. Miscellaneous Small Families (Lepidoptera)," The Great Lakes Entomologist, vol 35 (1) Available at: https://scholar.valpo.edu/tgle/vol35/iss1/10 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Voss: Moths of the Douglas Lake Region (Emmet and Cheboygan Counties), 2002 THE GREAT LAKES ENTOMOLOGIST 53 MOTHS OF THE DOUGLAS LAKE REGION (EMMET AND CHEBOYGAN COUNTIES), MICHIGAN: VI. MISCELLANEOUS SMALL FAMILIES (LEPIDOPTERA) Edward G. Voss1 ABSTRACT Forty-seven species in nine families of Lepidoptera (Hepialidae, Psychidae, Alucitidae, Sesiidae, Cossidae, Limacodidae, Thyrididae, Pterophoridae, Epiplemi- dae) are listed with earliest and latest recorded flight dates in Emmet and Cheboy- gan counties, which share the northern tip of the Lower Peninsula of Michigan. The records are from the principal institutional and private collections of Michigan moths and continue the documented listing of Lepidoptera in the region. ____________________ Emmet and Cheboygan counties share the northern tip of the Lower Peninsula of Michigan, the former bordered on the west by Lake Michigan and the latter, on the east by Lake Huron. -
Occasional Papers
NUMBER 136, 37 pages 28 August 2020 BISHOP MUSEUM OCCASIONAL PAPERS TAXONOMIC REVISION AND BIOGEOGRAPHY OF PHASSODES BETHUNE -B AKER , 1905 (L EPIDOPTERA : H EPIALIDAE ), GHOST MOTH DESCENDANTS OF A SUBDUCTION ZONE WEED IN THE SOUTH -WEST PACIFIC JOHN R. G REHAN & C ARLOS G.C. M IELKE BISHOP MUSEUM PRESS HONOLULU Cover illustration: Selection of scales from central forewing of Phassodes spp. (see page 14). Photos by James Boone, Miho Maeda, and Agnes Stubblefield. Bishop Museum Press has been publishing scholarly books on the natu - ESEARCH ral and cultural history of Hawai‘i and the Pacific since 1892. The R Bishop Museum Occasional Papers (eISSN 2376-3191) is a series of UBLICATIONS OF short papers describing original research in the natural and cultural sci - P ences. BISHOP MUSEUM The Bishop Museum Press also published the Bishop Museum Bulletin series. It was begun in 1922 as a series of monographs presenting the results of research in many scientific fields throughout the Pacific. In 1987, the Bulletin series was superceded by the Museum’s five current monographic series, issued irregularly: Bishop Museum Bulletins in Anthropology (eISSN 2376-3132) Bishop Museum Bulletins in Botany (eISSN 2376-3078) Bishop Museum Bulletins in Entomology (eISSN 2376-3124) Bishop Museum Bulletins in Zoology (eISSN 2376-3213) Bishop Museum Bulletins in Cultural and Environmental Studies (eISSN 2376-3159) To subscribe to any of the above series, or to purchase individual publi - cations, please write to: Bishop Museum Press, 1525 Bernice Street, Honolulu, Hawai‘i 96817-2704, USA. Phone: (808) 848-4135. Email: [email protected]. BERNICE PAUAHI BISHOP MUSEUM The State Museum of Natural and Cultural History eISSN 2376-3191 1525 Bernice Street Copyright © by Bishop Museum Honolulu, Hawai‘i 96817-2704, USA Published online: 28 August 2020 ISSN (online) 2376-3191 Taxonomic revision and biogeography of Phassodes Bethune-Baker, 1905 (Lepidoptera: Hepialidae), ghost moth descendants of a subduc - tion zone weed in the south-west Pacific. -
Predatory and Parasitic Lepidoptera: Carnivores Living on Plants
Journal of the Lepidopterists' Society 49(4), 1995, 412-453 PREDATORY AND PARASITIC LEPIDOPTERA: CARNIVORES LIVING ON PLANTS NAOMI E. PIERCE Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts, 02138, USA ABSTRACT. Moths and butterflies whose larvae do not feed on plants represent a decided minority slice of lepidopteran diversity, yet offer insights into the ecology and evolution of feeding habits. This paper summarizes the life histories of the known pred atory and parasitic lepidopteran taxa, focusing in detail on current research in the butterfly family Lycaenidae, a group disproportionately rich in aphytophagous feeders and myr mecophilous habits. More than 99 percent of the 160,000 species of Lepidoptera eat plants (Strong et al. 1984, Common 1990). Plant feeding is generally associated with high rates of evolutionary diversification-while only 9 of the 30 extant orders of insects (Kristensen 1991) feed on plants, these orders contain more than half of the total number of insect species (Ehrlich & Raven 1964, Southwood 1973, Mitter et al. 1988, cf. Labandiera & Sepkoski 1993). Phytophagous species are characterized by specialized diets, with fewer than 10 percent having host ranges of more than three plant families (Bernays 1988, 1989), and butterflies being particularly host plant-specific (e.g., Remington & Pease 1955, Remington 1963, Ehrlich & Raven 1964). This kind of life history specialization and its effects on population structure may have contributed to the diversification of phytophages by promoting population subdivision and isolation (Futuyma & Moreno 1988, Thompson 1994). Many studies have identified selective forces giving rise to differences in niche breadth (Berenbaum 1981, Scriber 1983, Rausher 1983, Denno & McClure 1983, Strong et al. -
(Non-Ditrysian) (1975),Davls
The LepidopterologicalSocietyLepidopterological Society of Japan 98 ec 8 ua Tyb to Ga Vol. 33, No. 1 & 2, 1982 3. Review of the Higher Classificatien of the Lepidoptera, with Special Referenee to Lower Heteroneuralls Ebbe Schmiclt NIELsEN Zoological Museum, Copenhagen, Denmark Present address: Division of Entomology, CSIRO, P.O, Box 1700, Canberra City, A.C,T. 2601, Australia Our knowledge ofthe phylogeny (on the suborder level) of the Lepidoptera has increased markedly during the last four decades. primarily because of increasing studies of the morphelogy and diversity of the primitive (non-ditrysian) Lepidoptera and because ef the ayailability of a well-reasoned meth- odology (HENNiG, 1966) for phylegenetic analysis. - The first phylogenetic classification of the Lepidoptera proposed by HENN[G (1953 mainly based on HiNToN7s (1946) obseryations) has since proved basically correct and has bcen further substantiated by several authors (see discussion and further references in CoMMoN (1975), DAvls (1978) and KRisTEN- SEN & NIELsEN (l980, 1981)), The presently recognized phylogeny of the lowest Lepidoptera is presented in Fig, 1, and the phylogeny of the Heteroneura is illustrated in Fig, 2. T7ze sister-gromp qf the LEPIDOI)7:ERA, The orders Lepidoptera and Trichoptera constitute the Amphiesmenoptera, the monophyly of which is generally accepted and considered among the best documented within the Insecta (HENNiG, 1969; KRIsTENsEN, 1975). A4bnophyly qf'the LEPIDOPTLERA. The monophyly of the Lepidoptera (including the Zeugloptera) is well documented by a suite of autapomorphies, some of which are: (1) absence of a median ocellus, (2) presence of a pit containing sensilla on apical segment of labial palp, (3) presence of rnedian posterior process on corporotentorium, (4) presence of protibial epiphysis and (5) presence of scale cover on wings (see discussion in KRisTENsEN, 1975). -
Remarks on Some Families of Leaf-Mining Microlepidoptera From
ConServaZione habiTaT inverTebraTi 5: 767–781 (2011) Cnbfvr Remarks on some families of leaf-mining Microlepidoptera from central-southern Sardinia, with some ecological considerations ( Lepidoptera: * Nepticulidae, Bucculatricidae, Gracillariidae) Paolo TRIBERTI1, Sonia BRAGGIO2 1c/o Museo Civico di Storia Naturale, Lungadige Porta Vittoria 9, I37129 Verona, Italy. Email: [email protected] 2Via Moron 20, I37024 Negrar (VR), Italy. Email: [email protected] *In: Nardi G., Whitmore D., Bardiani M., Birtele D., Mason F., Spada L. & Cerretti P. (eds), Biodiversity of Marganai and Montimannu (Sardinia). Research in the framework of the ICP Forests network. Conservazione Habitat Invertebrati, 5: 767–781. ABSTRACT Results of a faunistic study in Sardinia on three families of leaf miners (Microlepidoptera: Nepticulidae, Bucculatricidae and Gracillariidae) are presented. The study areas are located in the south-western and central-eastern parts of the island: the Linas-Oridda-Marganai Regional Park and the Golfo di Orosei and Gennargentu National Park. A total of 27 species are recorded, including 7 new for Sardinia and one (Trifurcula rosmarinella (Chrétien, 1914) (Nepticulidae)) new for Italy. Besides, in the family Nepticulidae the study of two species is still in progress whereas a third one, T. montana Lašt˚uvka Z., Lašt˚uvka A. & van Nieukerken, 2007, was recently described as new for science. In the faunistic list each species is ac- companied by a short comment on distribution and biology. Because of the notable supply of data in these last years, the list of all the species known from Sardinia of these three families is reported together with their hostplants. Particular attention is reserved to the evergreen oak leaf miners and the sampling of the mines of these insects is suggested for monitoring ecological changes. -
Amphiesmenoptera
AMPHIESMENOPTERA - the “garment wings” The Major Groups of Holometabola Holometabola (=Endopterygota) Order Hymenoptera Superorder Neuropterida Order Raphidioptera Order Megaloptera Order Neuroptera Order Coleoptera Order Strepsiptera, incertae sedis Superorder Mecopterida (= Panorpida) Antliophora Order Mecoptera - scorpionflies Order Siphonaptera - fleas Order Diptera - true flies Amphiesmenoptera Order Trichoptera - caddisflies Order Lepidoptera - butterflies & moths AMPHIESMENOPTERA - the “garment wings” SYNAPOMORPHIES • Adult prelabium fused with hypopharynx • Pronotum with paired setose “warts” • Wings with extensive covering of setae • Anal veins of the forewing apparently looping up into a double-Y configuration • Presence of paired glands opening on sternum V • Male genital segment IX with tergum and sternum fused, forming a closed ring AMPHIESMENOPTERA - the “garment wings” SYNAPOMORPHIES (continued) • Anterior margin of female segment VIII and IX with long, rodlike apodemes accommodating the insertion of protractor/retractor muscles on the extensible oviscapt • Female heterogamety (female is XY, male is XX) • Chromosome number specialized (high, n=30 in Trichoptera, n=31 in Lepidoptera) • Larval prelabium and hypopharynx fused into a lobe apically carrying the salivary (silk) gland orifice And many more (see Kristensen, N.P. 1984. Studies on the morphology and systematics of primitive Lepidoptera. Steenstrupia 10(5): 141-191; Kristensen, N.P. 1997. Early evolution of the Lepidoptera + Trichoptera lineage: phylogeny and the ecological -
Hepialids, with Morphological Evidence for the Phylogenetic Rela
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Arthropod Systematics and Phylogeny Jahr/Year: 2017 Band/Volume: 75 Autor(en)/Author(s): Simonsen Thomas J., Kristensen Nils Peter Artikel/Article: Revision of the endemic Brazilian ‘neotheorid’ hepialids, with morphological evidence for the phylogenetic relationships of the basal lineages of Hepialidae (Lepidoptera: Hepialoidea) 281-301 75 (2): 281 – 301 8.9.2017 © Senckenberg Gesellschaft für Naturforschung, 2017. Revision of the endemic Brazilian ‘neotheorid’ hepialids, with morphological evidence for the phylogenetic rela tionships of the basal lineages of Hepialidae (Lepido ptera: Hepialoidea) Thomas J. Simonsen *, 1, 2 & Niels P. Kristensen 3, # 1 Natural History Museum Aarhus, Wilhelm Meyers Allé 10, DK-8000 Aarhus C, Denmark; Thomas J. Simonsen * [[email protected]] — 2 Natural History Museum London, Cromwell Road, London, SW7 5BD, United Kingdom — 3 Natural History Museum of Denmark (Zoology), Universitetsparken 15, DK-2100 Copenhagen Ø, Denmark — * Corresponding author # This study was initiated as a collaborative effort between the authors in 2011. Sadly, Niels P. Kristensen passed away December 06, 2014, before the manuscript could be completed. He had, however, completed an extensive draft of the taxonomic sections of the text. It therefore seems most fitting that he remains first author of the names proposed here. Accepted 02.v.2017. Published online at www.senckenberg.de/arthropod-systematics on 30.viii.2017. Editors in charge: Ulrike Aspöck & Klaus-Dieter Klass Abstract We revise the little known South American primitive Hepialidae genus Neotheora Kristensen, and describe two new species, N. meyi sp.n. and N. -
Lepidoptera, Heteroneura: Monotrysia)
SYSTEMATICS AND PHYLOGENY OF HOLARCTIC GENERA OF NEPTICULIDAE (LEPIDOPTERA, HETERONEURA: MONOTRYSIA) by ERIK J. VAN NIEUKERKEN Nieukerken, E.J. van: Systematics and phylogeny of Holarctic genera of Nepticulidae (Lepidoptera, Heteroneura: Monotrysia). Zool. Verh. Leiden 236, 31-xii-1986: 1-93, figs. 1-135, tables 1-3. — ISSN 0024-1652. Key words: Lepidoptera; Monotrysia; Nepticulidae, phylogeny; hostplant relationships; leaf- miners. A revised classification of the Holarctic genera of Nepticulidae is provided. Eight genera belonging to the nominal subfamily are recognised and redefined. They are Enteucha Meyrick (= Johanssonia Borkowski, Artaversala Davis, Oligoneura Davis), Stigmella Schrank (including Astigmella Puplesis), Simplimorpha Scoble in the Nepticulini and Acalyptris Meyrick ( = Microcalyptris Braun, Niepeltia Strand), Trifurcula Zeller, Parafomoria Van Nieukerken, Bohemannia Stainton and Ectoedemia Busck in the Trifurculini. Trifurcula is divided into the subgenera Glaucolepis Braun (= Fedalmia Beirne), Levarchama Beirne and Trifurcula s.str. Ect- oedemia is divided into the subgenera Etainia Beirne, Fomoria Beirne, Laqueus Scoble, Zimmer- mannia Hering and Ectoedemia s.str. The genera and subgenera are (re)described and data on biology and distribution are given. The species Simplimorphapromissa (Staudinger) and Acalyp- tris psammophricta Meyrick are redescribed. A phylogeny of the family in cladistic sense is presented and discussed. The monophyly of Ectoedemia is uncertain, and monophyly of the subgenus Fomoria could not -
Lepidoptera of Canada 463 Doi: 10.3897/Zookeys.819.27259 REVIEW ARTICLE Launched to Accelerate Biodiversity Research
A peer-reviewed open-access journal ZooKeys 819: 463–505 (2019) Lepidoptera of Canada 463 doi: 10.3897/zookeys.819.27259 REVIEW ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Lepidoptera of Canada Gregory R. Pohl1, Jean-François Landry2, B. Chris Schmidt2, Jeremy R. deWaard3 1 Natural Resources Canada, Canadian Forest Service, 5320 – 122 St., Edmonton, Alberta, T6H 3S5, Canada 2 Agriculture and Agri-Food Canada, Ottawa Research and Development Centre, 960 Carling Avenue, Ottawa, Ontario, K1A 0C6, Canada 3 Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road East, Guelph, Ontario, N1G 2W1, Canada Corresponding author: Gregory R. Pohl ([email protected]) Academic editor: D. Langor | Received 6 June 2018 | Accepted 20 August 2018 | Published 24 January 2019 http://zoobank.org/D18E9BBE-EB97-4528-B312-70C3AA9C3FD8 Citation: Pohl GR, Landry J-F, Schmidt BC, deWaard JR (2019) Lepidoptera of Canada. In: Langor DW, Sheffield CS (Eds) The Biota of Canada – A Biodiversity Assessment. Part 1: The Terrestrial Arthropods. ZooKeys 819: 463–505. https://doi.org/10.3897/zookeys.819.27259 Abstract The known Lepidoptera (moths and butterflies) of the provinces and territories of Canada are summarised, and current knowledge is compared to the state of knowledge in 1979. A total of 5405 species are known to occur in Canada in 81 families, and a further 50 species have been reported but are unconfirmed. This represents an increase of 1348 species since 1979. The DNA barcodes available for Canadian Lepidoptera are also tabulated, based on a dataset of 148,314 specimens corresponding to 5842 distinct clusters.