DOCSLIB.ORG

Tesfu Et Al Checklist Lepidoptera Ethiopia.Pdf

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Tesfu Et Al Checklist Lepidoptera Ethiopia.Pdf No Family Scientific Name Author and year of Publication 1 Bedelliidae Bedellia somnulentella | (Zeller, 1847) 2 Blastobasidae Blastobasis eridryas Meyrick, 1932 3 Blastobasis industria Meyrick, 1913 4 Bombycidae Racinoa signicosta (Strand, 1911) 5 Bombyx mori (Linnaeus, 1758) 6 Brahmaeidae Dactyloceras widenmanni (Karisch, 1895) 7 Dactyloceras richinii Berio, 1940 8 Carposinidae Carposina candace Meyrick, 1932 9 Choreutidae Brenthia leucatoma Meyrick, 1918 10 Choreutis argyrastra Meyrick, 1932 11 Cosmopterigidae Ascalenia secretifera Meyrick, 1932 12 Cosmopterix derrai Koster, 2016 13 Cosmopterix epismaragda Meyrick, 1932 14 Cosmopteri trilopha Meyrick, 1922 15 Cossidae Aethalopteryx obscurascens (Gaede, 1930) 16 Aethalopteryx simillima (Hampson, 1916) 17 Afroarabiella stroheli Yakovlev & Witt, 2016 18 Azygophleps boisduvalii (Herrich-Schäffer, 1854) 19 Azygophleps brehmi Yakovlev & Witt, 2016 20 Azygophleps inclusa (Walker, 1856) 21 Camellocossus abyssinica (Hampson, 1910) 22 Camellocossus henleyi (Warren & Rothschild, 1905) 23 Camellocossus lalibela Yakovlev & Witt, 2017 24 Camellocossus strohlei Yakovlev & Witt, 2017 25 Eulophonotus myrmeleon Felder, 1874 26 Macrocossus sidamo (Rougeot, 1977) 27 Oreocossus kilimanjarensis (Holland, 1892) 28 Oreocossus occidentalis Strand, 1913 29 Oreocossus ungemachi Rougeot, 1977 1 30 Strigocossus kushit Yakovlev, 2011 31 Strigocossus mediopallens (Fletcher, 1968) 32 Crambidae Achyra coelatalis (Walker,1859) 33 Adelpherupa aethiopicalis Maes, 2002 34 Adelpherupa elongalis Maes, 2002 35 Aethaloessa floridalis Zeller, 1852 36 Agathodes dufayi Rougeot, 1977 37 Alphacrambus cristatus Bassi, 1995 38 Anania impunctata (Warren, 1897) 39 Ancylolomia argenteovittata Aurivillius, 1910 40 Ancylolomia gracilis Fawcett, 1918 41 Ancylolomia jacquelinae Rougeot, 1984 42 Ancylolomia inornata † Staudinger, 1870 43 Ancylolomia perfasciata Hampson, 1919 44 Ancylolomia planicosta Martin, 1956 45 Ancylolomia shafferi Rougeot, 1977 46 Ancylolomia shefferialis Rougeot, 1984 47 Angustalius hapaliscus (Zeller, 1852) 48 Autocharis ecthaemata (Hampson, 1913) 49 Bocchoris inspersalis (Zeller, 1852) 50 Cadarena pudoraria (Hübner, 1825) 51 Chalcidoptera thermographa Hampson, 1912 52 Chilo luniferalis Hampson, 1896 53 Chilo partellus (Swinhoe, 1885) 54 Classeya aphrodite Bleszynski, 1964 55 Classeya quadricuspis (Hampson, 1919) 56 Coniesta ignefusalis (Hampson, 1919) 57 Crambus arnaudiae Rougeot, 1977 58 Crambus bachi Bassi, 2012 59 Crambus bellinii Bassi, 2014 2 60 Crambus boislamberti (Rougeot, 1977) 61 Crambus caligula Bleszynski, 1961 62 Crambus dedalus Bassi, 2000 63 Crambus descarpentriesi (Rougeot, 1977) 64 Crambus diarhabdellus Hampson, 1919 65 Crambus jupiter Bleszynski, 1963 66 Crambus mesombrellus Hampson, 1919 67 Crambus netuncus Bassi, 2012 68 Crambus richteri Bleszynski, 1963 69 Crocidolomia pavonana (Fabricius, 1794) 70 Culladia achroellum (Mabille, 1900) 71 Dembea venulosella Ragonot, 1888 72 Diaphania indica (Saunders, 1851) 73 Diasemia lunalis Gaede, 1916 74 Diasemiopsis ramburiulis (Duponchel, 1834) 75 Dunposchelia lanceolalis (Guenée, 1854) 76 Eoophyla capensis (Hampson, 1906) 77 Eoophyla excentrica Mey & Speidel, 1999 78 Eoophyla nyasalis (Hampson, 1917) 79 Euchromius donum Schouten, 1988 80 Euchromius erum Schouten, 1988 81 Euchromius klimeschi Bleszynski, 1961 82 Euchromius tanalis Schouten, 1988 83 Euchromius ocellea (Haworth, 1811) 84 Euclasta gigantalis Viette, 1957 85 Euclasta sidamona Rougeot, 1977 86 Euclasta warreni Distant, 1892 87 Euctenospila castalis Warren, 1892 88 Ghesquierellana hirtusalis (Walker, 1859) 89 Glyphodes onychinalis (Guenée, 1854) 3 90 Heliothela ophideresana (Walker, 1863) 91 Hellula undalis (Fabricius, 1781) 92 Herpetogramma bipunctalis (Fabricius, 1794) 93 Herpetogramma licarsisalis (Walker, 1859) 94 Hodebertia testalis (Fabricius, 1794) 95 Hyalobathra dictatrix Meyrick, 1934 96 Hymenia perspectalis † (Hübner, 1796) Leucinodes ethiopica Mally, Korycinska, Agassiz, Hall, 97 Hodgetts & Nuss, 2015 98 Leucinodes laisalis (Walker, 1859) Leucinodes ugandensis Mally, Korycinska, Agassiz, Hall, 99 Hodgetts & Nuss, 2015 100 Lygropia nigricornis Hampson, 1898 101 Maruca vitrata (Fabricius, 1787) 102 Nomophila noctuella (Denis & Schiffermüller, 1775) 103 Noorda blitealis Walker, 1859 104 Noorda trimaculalis Amsel, 1965 105 Noorda unipunctalis Amsel, 1963 106 Notarcha quaternalis (Zeller, 1852) 107 Obtusipalpis brunneata Hampson, 1919 108 Obtusipalpis pardalis Hampson, 1896 109 Pagyda pulvereiumbralis (Hampson, 1918) 110 Palpita vitrealis (Rossi, 1794) 111 Parapoynx diminutalis Snellen, 1880 112 Parapoynx fluctuosalis (Zeller, 1852) 113 Parapoynx stagnalis (Zeller, 1852) 114 Pardomima callixantha Martin, 1955 115 Pardomima zanclophora Martin, 1955 116 Paschiodes mesoleucalis Hampson, 1913 117 Patania aegrotalis (Zeller, 1852) 118 Pediasia ferruginea Bleszynski, 1963 4 119 Pediasia simiensis Bleszynski, 1962 120 Prionapteryx selenalis (Hampson, 1919) 121 Prionotalis friesei Bleszynski, 1963 122 Prionotalis smaragdina (Butler, 1875) 123 Psara cryptolepis (Martin, 1956) 124 Pseudonoorda rubricostalis (Hampson, 1910) 125 Pycnarmon diaphana (Cramer, 1777) 126 Pyrausta centralis Maes, 2009 127 Pyrausta subflavalis (Warren, 1892) 128 Scirpophaga subumbrosa Meyrick, 1933 129 Spoladea recurvalis (Fabricius, 1775) 130 Surattha rufistrigalis Fawcett, 1918 131 Syllepte ovialis (Walker, 1859) 132 Synclera traducalis (Zeller, 1852) 133 Tegostoma richteri Amsel, 1963 134 Tegostoma subterminalis Hampson, 1918 135 Terastia subjectalis Lederer, 1863 136 Thyridphora furia (Swinhoe, 1884) 137 Udea ferrugalis (Hübner, 1796) 138 Ulopeza conigeralis Zeller, 1852 139 Uresiphita gilvata (Fabricius, 1794) 140 Zebronia phenice (Cramer, 1782) 141 Depressariidae Ethmia sabiella (Felder & Rogenhofer, 1875) 142 Odites ethiopicus Lvovsky, 2001 143 Drepanidae Gonoreta subtilis (Bryk, 1913) 144 Elachistidae Elachista delocharis Meyrick, 1932 145 Epermeniidae Epermenia meyi Gaedike, 2004 146 Erebidae Acantharctia nigrivena Rothschild, 1935 147 Acantholipes namacensis (Guenée, 1852) 148 Achaea albicilia (Walker, 1858) 5 149 Achaea catella Guenée, 1852 150 Achaea echo (Walker, 1858) 151 Achaea finita † (Guenée, 1852) 152 Achaea indeterminata (Walker, 1865) 153 Achaea lienardi (Boisduval, 1833) 154 Achaea monodi (Laporte, 1975) 155 Achaea obvia Hampson, 1913 156 Achaea praestans (Guenée, 1852) 157 Achaea regularidia (Strand, 1912) 158 Achaea trapezoides Guenée, 1862 159 Aedia albirena (Hampson, 1926) 160 Aedia pericyma Hampson, 1916 161 Aedia eurymelas Hampson 1916 162 Aedia konsonata Hacker, 2016 163 Aedia marmoreata Hacker, 2016 164 Aedia mesonephele Hampson 1916 165 Aedia politzari Hacker, 2016 166 Aedia sciras Fawcett, 1916 167 Aedia poliochroa (Hampson 1916) 168 Aedia squamosa (Wallengren, 1856) 169 Afrasura rivulosa ethiopica Durante, 2009 170 Afrasura indecisa orientalis Durante, 2009 171 Afrasura terlinea Durante, 2009 172 Afrojavanica kostlani (Gaede, 1923) 173 Afromurzinia lutescens (Walker, 1855) 174 Afrospilarctia lucida (Druce, 1898) 175 Alpenus diversata (Hampson, 1916) 176 Alpenus geminipuncta (Hampson, 1916) 177 Alpenus investigatorum (Karsch, 1898) 178 Alpenus maculosa (Stoll in Cramer, 1781) 6 179 Alpenus nigropunctata (Bethune-Baker, 1908) 180 Alpenus schraderi (Rothschild, 1910) 181 Alytarchia amanda (Boisduval, 1847) 182 Amata alicia (Butler, 1876) 183 Amata magrettii Berio, 1937 184 Amata ntebi (Bethune-Baker, 1911) 185 Amata rufina (Oberthür, 1878) 186 Amata shoa (Hampson, 1898) 187 Amata tomasina (Butler, 1876) 188 Amata velatipennis (Walker, 1864) 189 Amerila affinis (Rothschild, 1910) 190 Amerila bubo (Walker, 1855) 191 Amerila carneola (Hampson, 1916) 192 Amerila leucoptera (Hampson, 1901) 193 Amerila niveivitrea (Bartel, 1903) 194 Amerila puella (Fabricius, 1793) 195 Amerila vidua (Cramer, 1780) 196 Amerila vitrea (Plötz, 1880) 197 Amphicallia kostlani Strand, 1911 198 Amphicallia solai (Druce, 1907) 199 Amphicallia thelwalli tigris (Butler, 1883) 200 Amsactarctia pulchra (Rothschild, 1933) 201 Amsactarctia radiosa (Pagenstecher, 1903) 202 Amsactarctia venusta (Toulgoët, 1980) 203 Anoba trigonosema (Hampson, 1916) 204 Anoba disjuncta † (Walker, 1865) 205 Anomis erosa † (Hübner, 1810) 206 Anomis endochlora Hampson, 1926 207 Anomis flava (Fabricius, 1775) 208 Anomis luperca (Möschler, 1883) 7 209 Anomis sabulifera (Guenée, 1852) 210 Anticarsia rubricans Boisduval, 1833 211 Antiophlebia bourgognei Laporte, 1975 212 Apisa canescens Walker, 1855 213 Araeopteron alboniger Fiebiger & Hacker, 2001 214 Argyrostagma niobe (Weymer, 1896) 215 Aroa discalis (Walker, 1855) 216 Aroa quadriplagata Pagenstecher, 1903 217 Aroterosia punctineata (Hampson 1901) 218 Asota speciosa (Drury, 1773) 219 Asura xanthophaea Toulgoët, 1977 220 Asplenia melanodonta rubrescens Hampson, 1916 221 Attatha metaleuca Hampson, 1913 222 Audea blochwitzi Kuhne, 2005 223 Audea hemihyala (Karsch, 1896) 224 Audea melanoplaga (Hampson, 1902) 225 Audea paulumnodosa (Kühne, 2005) 226 Audea tegulata † Hampson, 1902 227 Audea zimmeri (Berio, 1954) 228 Autoba admota (Felder & Rogenhofer, 1874) 229 Automolis crassa (Felder, 1874) 230 Automolis pallida (Hampson, 1901) 231 Avatha ethiopica (Hampson.
Load more

Recommended publications
  • On the Taxonomy of the Genera Sesapa and Nipponasura (Lepidoptera, Erebidae, Arctiinae)
    Vestnik zoologii, 51(5): 369–374, 2017 DOI 10.1515/vzoo-2017-0044 UDC 595.78:57.06 ON THE TAXONOMY OF THE GENERA SESAPA AND NIPPONASURA (LEPIDOPTERA, EREBIDAE, ARCTIINAE) A. V. Volynkin Altai State University, Lenina st., 61, Barnaul, RF-656049 Russia Tomsk State University, Institute of Biology, Ecology, Soil Science, Agriculture and Forestry, Lenina Avenue, 36, Tomsk, RF-634050 Russia E-mail: [email protected] On the Taxonomy of the Genera Sesapa and Nipponasura (Lepidoptera, Erebidae, Arctiinae). Volynkin, A. V. — Statuses of the lithosiinae genera Sesapa Walker, 1854 and Nipponasura Inoue, 1965 are revised, Sesapa is treated as a valid distinct genus and Nipponasura is downgraded here as a subgenus of Sesapa. Male and female genitalia of Sesapa and male vesica of Nipponasura are described and illustrated for the fi rst time. A new combination is established: Sesapa (Sesapa) sanguinea (Moore, 1877), comb. n. Sesapa (Nipponasura) inouei Volynkin, nom. n. is introduced as replacement name for Nipponasura sanguinea Inoue, 1965. Key words: Lithosiini, Nudariina, Asia, Japan, China, revised status, replacement name, new combination. Introduction Th e Asura / Miltochrista generic complex is one of the largest and taxonomically most diffi cult Lithosiini groups including several hundreds of species distributed in Afrotropical, Oriental, Palaearctic and Australian Regions. Systematics of the Oriental and partly Palaearctic members of the generic complex was reviewed by Holloway (2001), and those of the Afrotropical members by Durante (2008; 2009; 2012). Th e genus Sesapa was erected by Walker (1854) for a single species Sesapa inscripta Walker, 1854. Hamp- son (1900) synonymized it with Miltochrista, and at present several other taxa originally described as Sesapa by diff erent authors (Butler, 1877; Moore, 1877) are placed to the genera Miltochrista and Barsine (Holloway, 2001; Kirti, Singh, 2015).
    [Show full text]
  • An Overview of Genera and Subgenera of the Asura / Miltochrista Generic Complex (Lepidoptera, Erebidae, Arctiinae)
    Ecologica Montenegrina 26: 14-92 (2019) This journal is available online at: www.biotaxa.org/em https://zoobank.org/urn:lsid:zoobank.org:pub:86F17262-17A8-40FF-88B9-2D4552A92F12 An overview of genera and subgenera of the Asura / Miltochrista generic complex (Lepidoptera, Erebidae, Arctiinae). Part 1. Barsine Walker, 1854 sensu lato, Asura Walker, 1854 and related genera, with descriptions of twenty new genera, ten new subgenera and a check list of taxa of the Asura / Miltochrista generic complex ANTON V. VOLYNKIN1,2*, SI-YAO HUANG3 & MARIA S. IVANOVA1 1 Altai State University, Lenina Avenue, 61, RF-656049, Barnaul, Russia 2 National Research Tomsk State University, Lenina Avenue, 36, RF-634050, Tomsk, Russia 3 Department of Entomology, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, China * Corresponding author. E-mail: [email protected] Received 30 October 2019 │ Accepted by V. Pešić: 2 December 2019 │ Published online 9 December 2019. Abstract Lithosiini genera of the Asura / Miltochrista generic complex related to Barsine Walker, 1854 sensu lato and Asura Walker, 1854 are overviewed. Barsine is considered to be a group having such an autapomorphic feature as a basal saccular process of valva only. Many species without this process are separated to the diverse and species-rich genus Ammatho stat. nov., which is subdivided here into eight subgenera including Idopterum Hampson, 1894 downgraded here to a subgenus level, and six new subgenera: Ammathella Volynkin, subgen. nov., Composine Volynkin, subgen. nov., Striatella Volynkin & Huang, subgen. nov., Conicornuta Volynkin, subgen. nov., Delineatia Volynkin & Huang, subgen. nov. and Rugosine Volynkin, subgen. nov. A number of groups of species considered previously by various authors as members of Barsine are erected here to 20 new genera and four subgenera: Ovipennis (Barsipennis) Volynkin, subgen.
    [Show full text]
  • Noctuoidea: Erebidae: Others
    Staude et al. / Metamorphosis 27: S165–S188 S165 ____________________________________________________________________________________________________________________________ Noctuoidea: Erebidae: Others Reference/ Lepidoptera Host plant Locality rearing no. Taxon Subfamily Family Taxon Family M1148 Anoba angulilinea Anobinae Erebidae Dalbergia Fabaceae Tshukudu Game melanoxylon Reserve, Hoedspruit M998 Anoba atripuncta Anobinae Erebidae Ormocarpum Fabaceae Tshukudu Game trichocarpum Reserve, Hoedspruit Gv71 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 14HSS52 Baniana arvorum Anobinae Erebidae Elephantorrhiza Fabaceae Steenkoppies, farm, elephantina Magaliesburg 13HSS84 Plecoptera arctinotata Anobinae Erebidae Senegalia caffra Fabaceae Steenkoppies, farm, Magaliesburg M1020a Plecoptera flaviceps Anobinae Erebidae Dalbergia Fabaceae Casketts, farm, melanoxylon Hoedspruit M317 Bareia incidens Calpinae Erebidae Ficus lutea Moraceae Casketts, farm, (unplaced as to Hoedspruit tribe) 14HSS87 Egnasia vicaria Calpinae Erebidae Afrocanthium Rubiaceae Dlinsa Forest, (unplaced as to mundianum Eshowe tribe) 12HSS163 Exophyla multistriata Calpinae Erebidae Celtis africana Cannabaceae Golden Valley, (unplaced as to Magaliesburg tribe) M416 Exophyla multistriata Calpinae Erebidae Trema orientalis Cannabaceae Sekororo, Tzaneen (unplaced as to (Fed on Celtis tribe) africana) M743 Lacera alope Calpinae Erebidae Pterolobium Fabaceae Moholoholo Rehab (unplaced as to stellatum Centre, Hoedspruit tribe)
    [Show full text]
  • Forestry Department Food and Agriculture Organization of the United Nations
    Forestry Department Food and Agriculture Organization of the United Nations Forest Health & Biosecurity Working Papers OVERVIEW OF FOREST PESTS INDONESIA January 2007 Forest Resources Development Service Working Paper FBS/19E Forest Management Division FAO, Rome, Italy Forestry Department Overview of forest pests - Indonesia DISCLAIMER The aim of this document is to give an overview of the forest pest1 situation in Indonesia. It is not intended to be a comprehensive review. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. © FAO 2007 1 Pest: Any species, strain or biotype of plant, animal or pathogenic agent injurious to plants or plant products (FAO, 2004). ii Overview of forest pests - Indonesia TABLE OF CONTENTS Introduction..................................................................................................................... 1 Forest pests...................................................................................................................... 1 Naturally regenerating forests..................................................................................... 1 Insects ..................................................................................................................... 1 Diseases..................................................................................................................
    [Show full text]
  • Comparative Morphology of the Male Genitalia in Lepidoptera
    COMPARATIVE MORPHOLOGY OF THE MALE GENITALIA IN LEPIDOPTERA. By DEV RAJ MEHTA, M. Sc.~ Ph. D. (Canta.b.), 'Univefsity Scholar of the Government of the Punjab, India (Department of Zoology, University of Oambridge). CONTENTS. PAGE. Introduction 197 Historical Review 199 Technique. 201 N ontenclature 201 Function • 205 Comparative Morphology 206 Conclusions in Phylogeny 257 Summary 261 Literature 1 262 INTRODUCTION. In the domains of both Morphology and Taxonomy the study' of Insect genitalia has evoked considerable interest during the past half century. Zander (1900, 1901, 1903) suggested a common structural plan for the genitalia in various orders of insects. This work stimulated further research and his conclusions were amplified by Crampton (1920) who homologized the different parts in the genitalia of Hymenoptera, Mecoptera, Neuroptera, Diptera, Trichoptera Lepidoptera, Hemiptera and Strepsiptera with those of more generalized insects like the Ephe­ meroptera and Thysanura. During this time the use of genitalic charac­ ters for taxonomic purposes was also realized particularly in cases where the other imaginal characters had failed to serve. In this con­ nection may be mentioned the work of Buchanan White (1876), Gosse (1883), Bethune Baker (1914), Pierce (1909, 1914, 1922) and others. Also, a comparative account of the genitalia, as a basis for the phylo­ genetic study of different insect orders, was employed by Walker (1919), Sharp and Muir (1912), Singh-Pruthi (1925) and Cole (1927), in Orthop­ tera, Coleoptera, Hemiptera and the Diptera respectively. It is sur­ prising, work of this nature having been found so useful in these groups, that an important order like the Lepidoptera should have escaped careful analysis at the hands of the morphologists.
    [Show full text]
  • Summer Butterflies in Dinosaur National Monument
    VOLUME 37, NUMBER 1 91 Journal of the Lepidopterists' Society 37(1), 1983, 91 SPECIES OF EUCALYPTUS AS FOOD PLANTS FOR LEPIDOPTERA IN EAST AFRICA Dr. 1. F. B. Common's paper, "Some factors responsible for imbalances in the Aus­ tralian fauna of Lepidoptera" (1981, J. Lepid. Soc. 34:286-294), and his remarks on the role of Eucalyptus as a lepidopterous food plant suggest that a list of the Lepidoptera feeding on the introduced Eucalyptus spp. in East Africa might be of interest. Various species of Eucalyptus are grown in many parts of East Africa, primarily as sources of firewood but also as useful agents in the reclamation of swampy land. E. citriodora is grown as a plantation crop in Zaire and elsewhere for its oil, used in the perfumery trade. The following is a list of species recorded as feeding on species of Eucalyptus: Lymantriidae-Euproctis molunduana Auriv., Dasychira georgiana Fawcett, D. basa­ lis Wlk., Argyrostagma niobe Weymer; Lasiocampidae---Lechriolepis nigrivenis Strand, Bombycopsis bipars Wlk., Nadiasa cuneata Distant, Pachypasa subfascia Wlk., P. pa­ pyri Tams, Eucraera salambo Vuillot; Saturniidae-Bunaea alcinoe Stoll, Nudaurelia conradsi Rebel, N. cytherea F., N. dione F., N. krucki Hering, N. gueinzii Karsch, Lobobunaea phaedusa Drury, Urota sinope Westwood, Athletes ethra Westwood; No­ todontidae-Desmeocraera varia Janse; Limacodidae-Latoia chapmanni Kirby; Psychidae-Eumeta rougeoti Bourgogne, Kotochalia junodi Hylaerts; Noctuidae­ Euxoa longidentifera Hampson, Spodoptera littoralis Bdv., Heliothis armigera (Hbn.), Anua mejanesi Gn., A. tirhaca Cramer, Achaea lienardi Bdv., A. catella Gn., A. faber Holland, PI usia limbirena Gn.; Geometridae-Orthonama obstipata F., Colocleom divisaria Wlk., Ascotis selenaria Schiff., A.
    [Show full text]
  • Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometro
    Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, & Noctuoidea) Biodiversity Inventory of the University of Florida Natural Area Teaching Lab Hugo L. Kons Jr. Last Update: June 2001 Abstract A systematic check list of 489 species of Lepidoptera collected in the University of Florida Natural Area Teaching Lab is presented, including 464 species in the superfamilies Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, and Noctuoidea. Taxa recorded in Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, and Thyrididae are also included. Moth taxa were collected at ultraviolet lights, bait, introduced Bahiagrass (Paspalum notatum), and by netting specimens. A list of taxa recorded feeding on P. notatum is presented. Introduction The University of Florida Natural Area Teaching Laboratory (NATL) contains 40 acres of natural habitats maintained for scientific research, conservation, and teaching purposes. Habitat types present include hammock, upland pine, disturbed open field, cat tail marsh, and shallow pond. An active management plan has been developed for this area, including prescribed burning to restore the upland pine community and establishment of plots to study succession (http://csssrvr.entnem.ufl.edu/~walker/natl.htm). The site is a popular collecting locality for student and scientific collections. The author has done extensive collecting and field work at NATL, and two previous reports have resulted from this work, including: a biodiversity inventory of the butterflies (Lepidoptera: Hesperioidea & Papilionoidea) of NATL (Kons 1999), and an ecological study of Hermeuptychia hermes (F.) and Megisto cymela (Cram.) in NATL habitats (Kons 1998). Other workers have posted NATL check lists for Ichneumonidae, Sphecidae, Tettigoniidae, and Gryllidae (http://csssrvr.entnem.ufl.edu/~walker/insect.htm).
    [Show full text]
  • Native Versus Exotic Crotalaria Species (Fabaceae) As Host Plants of the Ornate Bella Moth, Utetheisa Ornatrix (Lepidoptera: Erebidae: Arctiinae) Andrei Sourakov*
    Journal of Natural History, 2015 Vol. 49, Nos. 39–40, 2397–2415, http://dx.doi.org/10.1080/00222933.2015.1006700 You are what you eat: native versus exotic Crotalaria species (Fabaceae) as host plants of the Ornate Bella Moth, Utetheisa ornatrix (Lepidoptera: Erebidae: Arctiinae) Andrei Sourakov* McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA (Received 9 April 2014; accepted 2 January 2015; first published online 3 March 2015) Crotalaria plants and Utetheisa ornatrix are closely linked to each other: the larvae destroy the seeds, while the moth depends on hostplants for alkaloids. To better understand the ongoing co-evolution, the present study examines how native hos- tplants compare to exotic ones. Leaf-feeding on Crotalaria pumila, C. rotundifolia,and C. incana,nativetothemoth’s range, led to faster larval development than on the exotic C. lanceolata, C. spectabilis,andC. pallida. Seed-feeding on all species of Crotalaria led to accelerated larval development and a resultant larger adult moth, and correlates with a higher nitrogen content in the plant tissues. These results add a novel dimension to the previous studies of reproductive biology of this model organ- ism. In controlled settings, mature larvae showed preference for leaves of C. spectabilis over those of other species, perhaps due to the higher alkaloid content. Differences in morphology and phenology of Crotalaria determine the ecology of U. ornatrix popu- lations in Florida. The introduction of novel hostplants, on which U. ornatrix can have a significant negative effect and which are of concern to humans as invasive toxic weeds, has greatly expanded the niche occupied by this moth.
    [Show full text]
  • Occurrence and Distribution of Fall Armyworm, Spodoptera Frugiperda (Lepidoptera: Noctuidae) and Other Moths on Maize in Ghana B
    OCCURRENCE AND DISTRIBUTION OF FALL ARMYWORM, SPODOPTERA FRUGIPERDA (LEPIDOPTERA: NOCTUIDAE) AND OTHER MOTHS ON MAIZE IN GHANA By DJIMA KOFFI ID: 10600839 A THESIS SUBMITTED TO THE UNIVERSITY OF GHANA, LEGON IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE AWARD OF MASTER OF PHILOSOPHY (M.PHIL.) DEGREE IN ENTOMOLOGY. AFRICAN REGIONAL POSTGRADUATE PROGRAMME IN INSECT SCIENCE (ARPPIS) UNIVERSITY OF GHANA, LEGON, ACCRA, GHANA AUGUST, 2018 * JOINT INTER-FACULTY INTERNATIONAL PROGRAMME FOR THE TRAINING OF ENTOMOLOGISTS IN WEST AFRICA COLLABORATING DEPARTMENTS: ANIMAL BIOLOGY AND CONSERVATION SCIENCE (SCHOOL OF BIOLOGICAL SCIENCES) AND CROP SCIENCE (SCHOOL OF AGRICULTURE) COLLEGE OF BASIC AND APPLIED SCIENCES DECLARATION I hereby declare that this thesis is the result of the original work personally done by me for the award of a Master of Philosophy Degree in Entomology at the African Regional Postgraduate Programme in Insect Science (ARPPIS), University of Ghana, Legon. All the references to other people’s work have been duly acknowledged and this thesis has not been submitted in part or whole for the award of a degree elsewhere. Signature……………....................................... Date………………………………………….. DJIMA KOFFI (STUDENT) Signature……………....................................... Date………………………………………….. DR. ROSINA KYEREMATEN (PRINCIPAL SUPERVISOR) Signature……………....................................... Date………………………………………….. DR. VINCENT Y. EZIAH (CO-SUPERVISOR) Signature……………....................................... Date………………………………………….. DR.
    [Show full text]
  • Terrestrial Arthropod Surveys on Pagan Island, Northern Marianas
    Terrestrial Arthropod Surveys on Pagan Island, Northern Marianas Neal L. Evenhuis, Lucius G. Eldredge, Keith T. Arakaki, Darcy Oishi, Janis N. Garcia & William P. Haines Pacific Biological Survey, Bishop Museum, Honolulu, Hawaii 96817 Final Report November 2010 Prepared for: U.S. Fish and Wildlife Service, Pacific Islands Fish & Wildlife Office Honolulu, Hawaii Evenhuis et al. — Pagan Island Arthropod Survey 2 BISHOP MUSEUM The State Museum of Natural and Cultural History 1525 Bernice Street Honolulu, Hawai’i 96817–2704, USA Copyright© 2010 Bishop Museum All Rights Reserved Printed in the United States of America Contribution No. 2010-015 to the Pacific Biological Survey Evenhuis et al. — Pagan Island Arthropod Survey 3 TABLE OF CONTENTS Executive Summary ......................................................................................................... 5 Background ..................................................................................................................... 7 General History .............................................................................................................. 10 Previous Expeditions to Pagan Surveying Terrestrial Arthropods ................................ 12 Current Survey and List of Collecting Sites .................................................................. 18 Sampling Methods ......................................................................................................... 25 Survey Results ..............................................................................................................
    [Show full text]
  • Transactions of the Entomological Society of London
    — ( 309 ) XIX. Entomological Observations and Captures during the visit of the British Association to South Africa in 1905. By F. A. Dixey, M.A., M.D., F.E.S., and G. B. LoNGSTAFF, M.A., M.D., F.R.GP., F.E.S. [Read June 5th, 1907.] Plate XXV. Cape Town. Lat. 34° S. Sea level. August 8tli, 1905. Surely no one who was on deck when the " Kildonan Castle " anchored in Table Bay will forget the impressive scene. Behind the town-lights which gleamed along the front the grand mass of Table Mountain, clear cut against a streak of dawn, lay under the Southern Cross and Magellanic Clouds, while in the opposite quarter Jupiter and Venus shone brilliant beyond our experience, the latter reflected in the sea, and Orion standing on his head demonstrated that we were indeed in a Southern land. These astronomical facts had a bearing on our entomological operations, since we had to grow accus- tomed to the fact that the most promising hunting-grounds were slopes with a north-cast aspect. Faithful to our own science rather than to the associa- tion of which we were members, we had decided to go on to Durban by the same steamer, and put in as many days collecting as possible on the Natal Coast. This left us but a day and a half at Cape Town, in which to get a glimpse of its fauna and flora, and we were truly fortunate in that the Southern spring smiled upon us and provided, if indeed few insects, at any rate what Mr.
    [Show full text]
  • The Afrotropical Tiger-Moths
    46 JOURNAL OF THE LEPIDOPTERISTS' SOCIETY This .576 page special issue is composed of 12 papers in English and two new species are described. Similarly, in the Cosmopterigi­ ranging from the physical description of the Philippines to anno­ dae two new species are described and two new records are re­ tated checklists of several lepidopteran groups and one of Tri­ ported for the country. On a more ample basis, the Scopariinae and choptera and descriptions of several new taxa. Ten of the 12 papers Heliothelinae (Crambidae) of the Oriental region are reviewed; 11 are devoted to Lepidoptera, therefore this issue is of special interest genera and 63 species (including 6 new species) are recognized. This to the lepidopterist. paper includes diagnoses and phylogenetic remarks for the higher The following papers comprised the volume: "Short introduction taxa. In the last paper, a checklist of the fauna of caddis flies of the to Philippine natural and geological history and its relevance for Mt. Agtuuganon Range on Mindanao is presented. An amazing Lepidoptera" by C. G. Treadaway; "The Sphingidae (Lepidoptera) number 016.3 species out of the 102 listed are described and male of the Philippines" by W. Hogenes and C. G. Treadaway; The Lasio­ genitalia illustrated for the first time. campidae (Lepidoptera) of the Philippines by V V Zohouhin, C. G. It is important to note that special care was taken in order to in­ Treadaway and T. Witt; "The Satumiidae (Lepidoptera) of the Philip­ sure accuracy in the localities used in the distribution discussions or pines" by W A. Nassig and C.
    [Show full text]