DOCSLIB.ORG

Species List (PDF)

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Species List (PDF) NEPTICULIDAE PSYCHIDAE Stigmella sp. Kearfottia albifasciella (Fernald) Stigmella nr. unifasciella (Chambers) Cryptothelea gloverii (Packard) Oiketicus abbotii (Grote) OPOSTEGIDAE Pseudopostega albogaleriella (Clemens) BUCCULATRICIDAE Bucculatrix sp. #1 TISCHERIIDAE Bucculatrix sp. #2 Tischeria sp. #1 Bucculatrix sp. #3 Tischeria sp. #2 Bucculatrix staintonella (Chambers) Tischeria nr. quercitella (Clemens) GRACILLARIIDAE PRODOXIDAE Caloptilia sp. #1 Tegeticula yuccasella (Riley) Caloptilia sp. #2 Caloptilia sp. #3 ADELIDAE Caloptilia nr. blandella (Clemens) Adela caeruleella (Walker) Caloptilia nr. packardella (Fabricius) Caloptilia rhoifoliella (Chambers) ACROLOPHIDAE Caloptilia superbifrontella (Clemens) Amydria dyarella (Dietz) Caloptilia violacella (Clemens) Amydria margoriella (Dietz) Neurobathra sp. Acrolophus sp. #1 Neurobathra strigifinitella (Clemens) Acrolophus sp. #2 Lithocolletis sp. Acrolophus arcanella (Clemens) Cameraria sp. Acrolophus cressoni (Walsingham) Phyllocnistis citrella (Stainton) Acrolophus forbesi (Hasbrouck) Acrolophus heppneri (Davis) OECOPHORIDAE Acrolophus mycetophagus (Davis) Eupragia hospita (Hodges) Acrolophus piger (Dyar) Psilocorsis reflexella (Clemens) Acrolophus plumifrontella (Clemens) Autosticha kyotensis (Matsumura) Acrolophus popeanella (Clemens) Antaeotricha schlaegeri (Zeller) Acrolophus propinquus (Walsingham) Antaeotricha leucillana (Zeller) Acrolophus texanella (Chambers) Antaeotricha osseella (Walsingham) Antaeotricha humilis (Zeller) TENEIDAE Antaeotricha albulella (Walker) Nemapogon rileyi (Dietz) Rectiostoma xanthobasis (Zeller) Nemapogon variatella (Clemens) Inga sparsiciliella (Clemens) Diachorisia velatella (Clemens) Decantha boreasella (Chambers) Mea bipunctella (Dietz) Scardiella approximatella (Dietz) ELACHISTIDAE Diataga leptosceles (Walsingham) Elachista sp. #1 Xylesthia pruniramiella (Clemens) Elachista sp. #2 Tinea apicimaculella (Chambers) BLASTOBASIDAE Glyphidocera sp. 1 Glyphidocera floridanella (Busck) Aristotelia corallina (Walsingham) Glyphidocera lactiflosella (Chamber) Aristotelia ivae (Busck) Gerdana caritella (Busck) Aristotelia roseosuffusella (Clemens) Holococera sp. Aristotelia rubidella (Clemens) Holcocera crassicornella (Dietz) Evippe prunifoliella (Chambers) Calosima dianella (Dietz) Recurvaria sp. Calosima lucidella (Adamski) Coleotechnites sp.#1 Blastobasis sp. #1 Coleotechnites sp.#2 Blastobasis sp. #2 Coleotechnites sp.#3 Blastobasis sp. #3 Coleotechnites obliquistrigella (Chambers) Blastobasis sp. #4 Sinoe sp. Blastobasis glandulella (Riley) Exoteleia pinifoliella (Chambers) Hypatopa sp. Arogalea cristifasciella (Chambers) Telphusa latifasciella (Chambers) COLEOPHORIDAE Telphusa nr. sedulitella (Busck) Coleophora sp. #1 Symmetrischema striatella (Murtfeldt) Coleophora sp. #2 Chionodes sp. #1 Coleophora sp. #3 Chionodes sp. #2 Coleophora sp. #4 Chionodes discoocellella (Chambers) Batrachedra sp. Chionodes emptor (Hodges) Batrachedra busiris (Hodges) Chionodes pereyra (Clarke) Aroga compositella (Walker) MOMPHIDAE Fascista cercerisella (Chambers) Mompha sp. Stegasta bosqueella (Chambers) Mompha eloisella (Clemens) Polyhymno luteostrigella (Chambers) Ymeldia janae (Hodges) COSMOPTERIGIDAE Untomia nr. albistrigella (Chambers) Euclemensia bassettella (Clemens) Battaristis sp. Cosmopterix nitens (Walsingham) Battaristis vittella (Busck) Cosmopterix pulchrimella (Chambers) Anacampsis conclusella (Walker) Cosmopterix attenuatella (Walker) Anacampsis coverdalella (Kearfott) Cosmopterix dapifera (Hodges) Strobisia iridipennella (Clemens) Cosmopterix abdita (Hodges) Helcystogramma chambersella (Murtfeldt) Cosmopterix scirpicola (Hodges) Dichomeris sp. Cosmopterix ebriola (Hodges) Dichomeris ligulella (Hübner) Melanocinclis lineigera (Hodges) Dichomeris punctidiscella (Clemens) Pyroderces rileyi (Walsingham) Dichomeris acuminata (Staudinger) Pyroderces badia (Hodges) Dichomeris nenia (Hodges) Limnaecia phragmitella (Stainton) Dichomeris ventrella (Fitch) Siskiwitia falcata (Hodges) Dichomeris punctipennella (Clemens) Perimede erransella (Chambers) Dichomeris setosella (Clemens) Perimede falcata (Braun) Dichomeris vindex (Hodges) Dichomeris aglaia (Hodges) GELECHIIDAE Dichomeris inversella (Zeller) Aristotelia sp. #1 Dichomeris kimballi (Hodges) Aristotelia sp. #2 2 GLYPHIPTERIGIDAE Glaphyria cappsi (Munroe) Diploschizia lanista (Meyrick) Aethiophysa lentiflualis (Zeller) Diploschizia habecki (Heppner) Lipocosma septa (Munroe) Diploschizia impigritella (Clemens) Lipocosmodes fuliginosalis (Fernald) Dicymolomia julianalis (Walker) PLUTELLIDAE Dicymolomia metalophota (Hampson) Plutella porrectella (Linnaeus) Dicymolomia grisea (Munroe) Plutella xylostella (Linnaeus) Chalcoela pegasalis (Walker) Oenobotys vinotinctalis (Hampson) ATTEVIDAE Crocidophora pustuliferalis (Lederer) Atteva pustulella (Fabricius) Crocidophora tuberculalis (Lederer) Ostrinia penitalis (Grote) YPONOMEUTIDAE Ostrinia obumbratalis (Lederer) Zelleria retiniella (Forbes) Perispasta caeculalis (Zeller) Nealgedonia extricalis (Guenée) LYONETIIDAE Hahncappsia marculenta (Grote & Philonome sp. Robinson) Leucoptera erythrinella (Busck) Neohelvibotys neohelvialis (Capps) Neohelvibotys polingi (Capps) PYRALIDAE Uresiphita reversalis (Guenée) Pyrausta signatalis (Walker) Group Crambinina Pyrausta bicoloralis (Guenée) Scoparia biplagialis (Walker) Pyrausta phoenicealis (Hübner) Eudonia strigalis (Dyar) Pyrausta tyralis (Guenée) Eudonia heterosalis (McDunnough) Hyalorista taeniolalis (Guenée) Undulambia polystichalis (Capps) Udea rubigalis (Guenée) Neocataclysta magnificalis (Hübner) Lineodes fontella (Walsingham) Munroessa sp. Lineodes integra (Zeller) Munroessa icciusalis (Walker) Loxostegopsis merrickalis (Barnes & Munroessa nebulosalis (Fernald) McDunnough) Munroessa gyralis (Hulst) Eurrhyparodes lygdamis (Druce) Nymphuliella daeckealis (Haimbach) Diacme elealis (Walker) Synclita tinealis (Munroe) Diacme phyllisalis (Walker) Synclita obliteralis (Walker) Niphograpta albiguttalis (Warren) Parapoynx maculalis (Clemens) Samea ecclesialis (Guenée) Parapoynx obscuralis (Grote) Samea multiplicalis (Guenée) Paraponyx seminealis (Walker) Samea baccatalis (Hulst) Parapoynx allionealis (Walker) Nomophila nearctica (Munroe) Parapoynx diminutalis (Snellen) Ategumia ebulealis (Guenée) Eoparargyractis irroratalis (Dyar) Desmia funeralis (Hübner) Eustixia pupula (Hübner) Desmia maculalis (Westwood) Microtheoris ophionalis (Walker) Desmia subdivisalis (Grote) Hellula rogatalis (Hulst) Desmia ploralis (Guenée) Glaphyria glaphyralis (Guenée) Hymenia perspectalis (Hübner) Glaphyria sp. Spoladea recurvalis (Fabricius) Glaphyria sesquistrialis (Hübner) Diasemiopsis leodocusalis (Walker) 3 Anageshna primordialis (Dyar) Urola nivalis (Drury) Apogeshna stenialis (Guenée) Vaxi auratella (Clemens) Blepharomastix ranalis (Guenée) Diatraea evanescens (Dyar) Glyphodes sibillalis (Walker) Diatraea lisetta (Dyar) Colomychus talis (Grote) Haimbachia squamulella (Zeller) Diaphania hyalinata (Linneaus) Eoreuma densella (Zeller) Diaphania modialis (Dyar) Xubida linearella (Zeller) Palpita quadristigmalis (Guenée) Xubida panalope (Dyar) Palpita illibalis (Hübner) Palpita magniferalis (Walker) Group Pyralinina Polygrammodes flavidalis (Guenée) Pyralis farinalis (Linneaus) Agathodes designalis (Guenée) Aglossa cuprina (Zeller) Pantographa limata (Grote & Robinson) Pseudasopia intermedialis (Walker) Pleuroptya silicalis (Guenée) Dolichomia binodulalis (Zeller) Psara obscuralis (Lederer) Dolichomia olinalis (Guenée) Bicilia iarchasalis (Walker) Ocrasa nostralis (Guenée) Herpetogramma bipunctalis (Fabricius) Parachma ochracealis (Walker) Herpetogramma phaeopteralis (Guenée) Basacallis tarachodes (Cashatt) Herpetogramma theseusalis (Walker) Lepidomys irrenosa (Guenée) Herpetogramma aeglealis (Walker) Galasa nigrinodis (Zeller) Pilocrocis ramentalis (Lederer) Tosale oviplagalis (Walker) Syngamia florella (Stoll) Clydonopteron sacculana (Bosc) Marasmia cochrusalis (Walker) Arta statalis (Grote) Leptosteges flavicostella (Fernald) Xantippe uranides (Dyer) Carectocultus perstrialis (Hübner) Heliades mulleolella (Hulst) Carectocultus repugnatalis (Walker) Macalla superatalis (Clemens) Rupela tinctella (Walker) Macalla zelleri (Grote) Donacaula sordidella (Zincken) Deuterollyta majuscula [= Jocara Donacaula unipunctella (Robinson) incrustalis] (Herrich-Schäffer) Donacaula maximella (Fernald) Oneida lunulalis (Hulst) Crambus praefectellus (Zincken) Tallula atramentalis (Lederer) Crambus sanfordellus (Klots) Tallula atrifascialis (Hulst) Crambus quinquareatus (Zeller) Pococera sp. Crambus caliginosellus (Clemens) Pococera robustella (Zeller) Raphiptera argillaceella (Packard) Pococera subcanalis (Walker) Microcrambus biguttellus (Forbes) Pococera militella (Zeller) Microcrambus elegans (Clemens) Pococera aplastella (Hulst) Microcrambus minor (Forbes) Galleria mellonella (Linnaeus) Fissicrambus profanellus (Walker) Omphalocera munroei (Martin) Fissicrambus haytiellus (Zincken) Acrobasis indigenella (Zeller) Fissicrambus hemiochrellus (Zeller) Acrobasis sp. #1 Fissicrambus mutabilis (Clemens) Acrobasis sp. #2 Parapediasia decorella (Zincken) Acrobasis vaccinii (Riley) Parapediasia teterrella (Zincken) Acrobasis minimella (Ragonot) Euchromius ocelleus (Haworth) Acrobasis stigmella (Dyar) Argyria lacteella (Fabricius) Acrobasis exsulella (Zeller) 4 Acrobasis demotella (Grote) Sphenarches anisodactylus (Walsingham) Acrobasis cirroferella (Hulst) Buckleria parvulus (Barnes & Lindsey) Anabasis ochrodesma (Zeller) Lantanophaga pusillidactylus (Walker)
Load more

Recommended publications
  • Bon Echo Provincial Park
    BON ECHO PROVINCIAL PARK One Malaise trap was deployed at Bon Echo Provincial Park in 2014 (44.89405, -77.19691 278m ASL; Figure 1). This trap collected arthropods for twenty weeks from May 7 – September 24, 2014. All 10 Malaise trap samples were processed; every other sample was analyzed using the individual specimen protocol while the second half was analyzed via bulk analysis. A total of 2559 BINs were obtained. Over half the BINs captured were flies (Diptera), followed by bees, ants and wasps (Hymenoptera), moths and butterflies (Lepidoptera), and beetles (Coleoptera; Figure 2). In total, 547 arthropod species were named, representing 22.9% of the BINs from the site (Appendix 1). All BINs were assigned at least to Figure 1. Malaise trap deployed at Bon Echo family, and 57.2% were assigned to a genus (Appendix Provincial Park in 2014. 2). Specimens collected from Bon Echo represent 223 different families and 651 genera. Diptera Hymenoptera Lepidoptera Coleoptera Hemiptera Mesostigmata Trombidiformes Psocodea Sarcoptiformes Trichoptera Araneae Entomobryomorpha Symphypleona Thysanoptera Neuroptera Opiliones Mecoptera Orthoptera Plecoptera Julida Odonata Stylommatophora Figure 2. Taxonomy breakdown of BINs captured in the Malaise trap at Bon Echo. APPENDIX 1. TAXONOMY REPORT Class Order Family Genus Species Arachnida Araneae Clubionidae Clubiona Clubiona obesa Linyphiidae Ceraticelus Ceraticelus atriceps Neriene Neriene radiata Philodromidae Philodromus Salticidae Pelegrina Pelegrina proterva Tetragnathidae Tetragnatha Tetragnatha shoshone
    [Show full text]
  • 1 1 DNA Barcodes Reveal Deeply Neglected Diversity and Numerous
    Page 1 of 57 1 DNA barcodes reveal deeply neglected diversity and numerous invasions of micromoths in 2 Madagascar 3 4 5 Carlos Lopez-Vaamonde1,2, Lucas Sire2, Bruno Rasmussen2, Rodolphe Rougerie3, 6 Christian Wieser4, Allaoui Ahamadi Allaoui 5, Joël Minet3, Jeremy R. deWaard6, Thibaud 7 Decaëns7, David C. Lees8 8 9 1 INRA, UR633, Zoologie Forestière, F- 45075 Orléans, France. 10 2 Institut de Recherche sur la Biologie de l’Insecte, UMR 7261 CNRS Université de Tours, UFR 11 Sciences et Techniques, Tours, France. 12 3Institut de Systématique Evolution Biodiversité (ISYEB), Muséum national d'Histoire naturelle, 13 CNRS, Sorbonne Université, EPHE, 57 rue Cuvier, CP 50, 75005 Paris, France. 14 4 Landesmuseum für Kärnten, Abteilung Zoologie, Museumgasse 2, 9020 Klagenfurt, Austria 15 5 Department of Entomology, University of Antananarivo, Antananarivo 101, Madagascar 16 6 Centre for Biodiversity Genomics, University of Guelph, 50 Stone Road E., Guelph, ON 17 N1G2W1, Canada 18 7Centre d'Ecologie Fonctionnelle et Evolutive (CEFE UMR 5175, CNRS–Université de Genome Downloaded from www.nrcresearchpress.com by UNIV GUELPH on 10/03/18 19 Montpellier–Université Paul-Valéry Montpellier–EPHE), 1919 Route de Mende, F-34293 20 Montpellier, France. 21 8Department of Life Sciences, Natural History Museum, Cromwell Road, SW7 5BD, UK. 22 23 24 Email for correspondence: [email protected] For personal use only. This Just-IN manuscript is the accepted prior to copy editing and page composition. It may differ from final official version of record. 1 Page 2 of 57 25 26 Abstract 27 Madagascar is a prime evolutionary hotspot globally, but its unique biodiversity is under threat, 28 essentially from anthropogenic disturbance.
    [Show full text]
  • 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.
    [Show full text]
  • Lepidoptera of North America 5
    Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains,
    [Show full text]
  • Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
    Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11
    [Show full text]
  • Insect Survey of Four Longleaf Pine Preserves
    A SURVEY OF THE MOTHS, BUTTERFLIES, AND GRASSHOPPERS OF FOUR NATURE CONSERVANCY PRESERVES IN SOUTHEASTERN NORTH CAROLINA Stephen P. Hall and Dale F. Schweitzer November 15, 1993 ABSTRACT Moths, butterflies, and grasshoppers were surveyed within four longleaf pine preserves owned by the North Carolina Nature Conservancy during the growing season of 1991 and 1992. Over 7,000 specimens (either collected or seen in the field) were identified, representing 512 different species and 28 families. Forty-one of these we consider to be distinctive of the two fire- maintained communities principally under investigation, the longleaf pine savannas and flatwoods. An additional 14 species we consider distinctive of the pocosins that occur in close association with the savannas and flatwoods. Twenty nine species appear to be rare enough to be included on the list of elements monitored by the North Carolina Natural Heritage Program (eight others in this category have been reported from one of these sites, the Green Swamp, but were not observed in this study). Two of the moths collected, Spartiniphaga carterae and Agrotis buchholzi, are currently candidates for federal listing as Threatened or Endangered species. Another species, Hemipachnobia s. subporphyrea, appears to be endemic to North Carolina and should also be considered for federal candidate status. With few exceptions, even the species that seem to be most closely associated with savannas and flatwoods show few direct defenses against fire, the primary force responsible for maintaining these communities. Instead, the majority of these insects probably survive within this region due to their ability to rapidly re-colonize recently burned areas from small, well-dispersed refugia.
    [Show full text]
  • Moth Checklist Pagemaker
    thePembrokeAreaFieldNaturalists presents a MothChecklist of central Renfrew County, Ontario compiled by Jason J. Dombroskie ©chris michener February 2003 Checklist of Moths of the Pembroke Area Field Naturalists Compiled by Jason J. Dombroskie. Status: VR = very rare, R = rare, U = uncommon, C = common Scientific Name Common Name status Family Hepialidae Ghost Moths Sthenopis argenteomaculatus (Harris) Silver-spotted Ghost Moth U Sthenopis quadriguttatus (Grote) Four-spotted Ghost Moth U Family Nepticulidae Minute Eye-cap Moths Ectoedemia populella Busck Poplar Petiolegall Moth C Ectoedemia ulmella (Braun) C Glaucolepis saccharella (Braun) Stigmella corylifoliella (Clemens) U Stigmella saginella (Clemens) R Family Heliozelidae Shield Bearer Moths Antispila freemani Lafontaine R Family Adelidae Fairy Moths Adela purpurea Walker Willow Fairy Moth U Family Incurvariidae Leafcutter Moths Paraclemensia acerifoliella (Fitch) Maple Leafcutter C Family Tineidae Fungus Moths Eccritothrix trimaculella (Chambers) R Nemapogon granella (Linnaeus) R Family Gracillariidae Leaf Miner Moths Caloptilia fraxinella (Ely) Privet Leaf Miner C Caloptilia invariabilis (Braun) Cherry Leafcone Caterpillar C Caloptilia near stigmatella (Fabricus) C Caloptilia umbratella (Braun) R Parornix crataegifoliella (Clemens) R Parornix inusitatumella (Chambers) R Phyllonorycter aeriferella (Clemens) R Phyllonorycter argentifimbriella (Clemens) R Phyllonorycter basistrigella (Clemens) R Phyllonorycter lucetiella (Clemens) Basswood Squareblotch Miner U Phyllonorycter ostryaefoliella
    [Show full text]
  • First Report of Native Parasitoids of Fall Armyworm Spodoptera Frugiperda Smith (Lepidoptera: Noctuidae) in Mozambique
    insects Article First Report of Native Parasitoids of Fall Armyworm Spodoptera frugiperda Smith (Lepidoptera: Noctuidae) in Mozambique Albasini Caniço 1,2,3,* , António Mexia 1 and Luisa Santos 4 1 LEAF-Linking Landscape, Environment, Agriculture and Food- School of Agriculture—University of Lisbon, Tapada da Ajuda, 1349-017 Lisbon, Portugal; [email protected] 2 Division of Agriculture—The Polytechnic of Manica (ISPM), District of Vanduzi, Matsinho 2200, Mozambique 3 Postgraduate Program Science for Development (PGCD), Gulbenkian Institute of Science, Rua da Quinta Grande 6, 2780-156 Oeiras, Portugal 4 Department of Plant Protection-Faculty of Agronomy and Forestry Engineering, Eduardo Mondlane University, P.O. Box 257, Maputo 1102, Mozambique; [email protected] * Correspondence: [email protected]; Tel.: +351-21-365-3128 (ext. 3428) Received: 13 August 2020; Accepted: 7 September 2020; Published: 8 September 2020 Simple Summary: In 2016, a highly destructive insect pest with origin in the Americas was detected in Africa. The pest is known to feed primarily on maize which is a staple food in the continent. Since then, farmers have been using chemical insecticides to control the pest. Chemical insecticides are expensive and harmful to the environment. In this article, the authors Albasini Caniço, António Mexia, and Luisa Santos discuss the possibility of application of an alternative method of control known to be environmentally friendly and economically sustainable in the long term. The method, known as “biological control”, can be easily implemented by farmers, and has the potential to reduce the population of the insect pest and production costs, and bring long term benefits to the environment.
    [Show full text]
  • JAVELIN WG® Spray Must Be Deposited at the Larval Feeding Site
    For Control of Insect Pests of Vegetables, Fruit and Field Crops ACTIVE INGREDIENT: Bacillus thuringiensis, subspecies kurstaki strain SA-11 solids, spores, and Lepidopteran active toxins* .............................................................................. 85.0% OTHER INGREDIENTS: ........................................................................................ 15.0% TOTAL 100.0% * The percentage active ingredient does not indicate product performance and potency measurements are not federally standardized. KEEP OUT OF REACH OF CHILDREN CAUTION See additional precautionary statements EPA REG. NO.: 70051-66 Lot No. EPA EST. NO.: Net Contents: Manufactured by: Certis USA LLC ESL 20160825 9145 Guilford Road, Suite 175 rev20191112 Columbia, MD 21046 This is a Specimen Label. It may not reflect the most-recent approved label for use in your state. Always refer to the label on the product packaging for approved use instructions. Please contact your Certis sales representative for more information. Page 1 of 17 PRECAUTIONARY STATEMENTS HAZARDS TO HUMANS AND DOMESTIC ANIMALS CAUTION. Harmful if absorbed through skin. Avoid contact with skin, eyes or clothing. Wash thoroughly with soap and water after handling and before eating, drinking, chewing gum, using tobacco, or using the toilet. Remove and wash contaminated clothing before reuse. Harmful if inhaled. Avoid breathing spray mist. Prolonged or frequently repeated skin contact may cause allergic reactions in some individuals. FIRST AID If on skin or clothing: Take off contaminated clothing. Rinse skin immediately with plenty of water for 15-20 minutes. If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes. Remove contact lenses, if present, after the first 5 minutes, then continue rinsing eye. If inhaled: Move person to fresh air.
    [Show full text]
  • Conservation and Management of Eastern Big-Eared Bats a Symposium
    Conservation and Management of Eastern Big-eared Bats A Symposium y Edited b Susan C. Loeb, Michael J. Lacki, and Darren A. Miller U.S. Department of Agriculture Forest Service Southern Research Station General Technical Report SRS-145 DISCLAIMER The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. Papers published in these proceedings were submitted by authors in electronic media. Some editing was done to ensure a consistent format. Authors are responsible for content and accuracy of their individual papers and the quality of illustrative materials. Cover photos: Large photo: Craig W. Stihler; small left photo: Joseph S. Johnson; small middle photo: Craig W. Stihler; small right photo: Matthew J. Clement. December 2011 Southern Research Station 200 W.T. Weaver Blvd. Asheville, NC 28804 Conservation and Management of Eastern Big-eared Bats: A Symposium Athens, Georgia March 9–10, 2010 Edited by: Susan C. Loeb U.S Department of Agriculture Forest Service Southern Research Station Michael J. Lacki University of Kentucky Darren A. Miller Weyerhaeuser NR Company Sponsored by: Forest Service Bat Conservation International National Council for Air and Stream Improvement (NCASI) Warnell School of Forestry and Natural Resources Offield Family Foundation ContEntS Preface . v Conservation and Management of Eastern Big-Eared Bats: An Introduction . 1 Susan C. Loeb, Michael J. Lacki, and Darren A. Miller Distribution and Status of Eastern Big-eared Bats (Corynorhinus Spp .) . 13 Mylea L. Bayless, Mary Kay Clark, Richard C. Stark, Barbara S.
    [Show full text]
  • Lepidoptera Recorded for Imperial County California Compiled by Jeffrey Caldwell [email protected] 1-925-949-8696 Note
    Lepidoptera Recorded for Imperial County California Compiled by Jeffrey Caldwell [email protected] 1-925-949-8696 Note: BMNA = Butterflies and Moths of North America web site MPG = Moth Photographers Group web site Most are from the Essig Museum’s California Moth Specimens Database web site Arctiidae. Tiger and Lichen Moths. Apantesis proxima (Notarctia proxima). Mexican Tiger Moth. 8181 [BMNA] Ectypia clio (clio). Clio Tiger Moth. 8249 Estigmene acrea (acrea). Salt Marsh Moth. 8131 Euchaetes zella. 8232 Autostichidae (Deoclonidae). Oegoconia novimundi. Four-spotted Yellowneck Moth. 1134 (Oegoconia quadripuncta mis-applied) Bucculatricidae. Ribbed Cocoon-maker Moths. Bucculatrix enceliae. Brittlebrush Moth. 0546 Cossidae. Goat Moths, Carpenterworm Moths, and Leopard Moths. Comadia henrici. 2679 Givira mucida. 2660 Hypopta palmata. 2656 Prionoxystus robiniae (mixtus). Carpenterworm or Locust Borer. 2693 Depressariidae. Pseudethmia protuberans. 1008 [MPG] Ethmiidae. Now assigned to Depressariidae. Ethmiinae. Ethmia timberlakei. 0984 Pseudethmia protuberans. 1008 Gelechiidae. Twirler Moths. Aristotelia adceanotha. 1726 [Sighting 1019513 BMNA] Chionodes abdominella. 2054 Chionodes dentella. 2071 Chionodes fructuaria. 2078 Chionodes kincaidella. 2086 (reared from Atriplex acanthocarpa in Texas) Chionodes oecus. 2086.2 Chionodes sistrella. 2116 Chionodes xanthophilella. 2125 Faculta inaequalis. Palo Verde Webworm. 2206 Friseria cockerelli. Mesquite Webworm. 1916 Gelechia desiliens. 1938 Isophrictis sabulella. 1701 Keiferia lycopersicella. Tomato Pinworm. 2047 Pectinophora gossypiella. Pink Bollworm. 2261 Prolita puertella. 1895 Prolita veledae. 1903 Geometridae. Inchworm Moths, Loopers, Geometers, or Measuring Worms. Archirhoe neomexicana. 7295 Chesiadodes coniferaria. 6535 Chlorochlamys appellaria. 7073 Cyclophora nanaria. Dwarf Tawny Wave. W 7140 Dichorda illustraria. 7055 Dichordophora phoenix. Phoenix Emerald. 7057 Digrammia colorata. Creosote Moth. 6381 Digrammia irrorata (rubricata). 6395 Digrammia pictipennata. 6372 Digrammia puertata.
    [Show full text]
  • Download Download
    UNIVERSITY THOUGHT doi:10.5937/univtho7-15336 Publication in Natural Sciences, Vol. 7, No. 2, 2017, pp. 1-27. Original Scientific Paper A CONTRIBUTION TO KNOWLEDGE OF THE BALKAN LEPIDOPTERA. SOME PYRALOIDEA (LEPIDOPTERA: CRAMBIDAE & PYRALIDAE) ENCOUNTERED RECENTLY IN SOUTHERN SERBIA, MONTENEGRO, THE REPUBLIC OF MACEDONIA AND ALBANIA COLIN W. PLANT1*, STOYAN BESHKOV2, PREDRAG JAKŠIĆ3, ANA NAHIRNIĆ2 114 West Road, Bishops Stortford, Hertfordshire, CM23 3QP, England 2National Museum of Natural History, Sofia, Bulgaria 3Faculty of Natural Science and Mathematics, University of Priština, Kosovska Mitrovica, Serbia ABSTRACT Pyraloidea (Lepidoptera: Crambidae & Pyralidae) were sampled in the territories of southern Serbia, Montenegro, the Former Yugoslav Republic of Macedonia and Albania on a total of 53 occasions during 2014, 2016 and 2017. A total of 173 species is reported here, comprising 97 Crambidae and 76 Pyralidae. Based upon published data, 29 species appear to be new to the fauna of Serbia, 5 species are new to the fauna of Macedonia and 37 are new to the fauna of Albania. The data are discussed. Keywords: Faunistics, Serbia, Montenegro, Republic of Macedonia, Albania, Pyraloidea, Pyralidae, Crambidae. of light trap. Some sites were visited on more than one occasion; INTRODUCTION others were sampled once only. Pyraloidea (Lepidoptera: Crambidae and Pyralidae) have As a by-product of this work, all remaining material from been examined in detail in the neighbouring territory of the the traps was returned to Sofia where Dr Boyan Zlatkov was Republic of Bulgaria and the results have been published by one given the opportunity to extract the Tortricoidea. The remaining of us (Plant, 2016). That work presented data for the 386 species material was retained and sent by post to England after the end of and 3 additional subspecies known from that country.
    [Show full text]