Lepidoptera: Nolidae) Moths from Korea
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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. -
Biodiversity and Ecology of Critically Endangered, Rûens Silcrete Renosterveld in the Buffeljagsrivier Area, Swellendam
Biodiversity and Ecology of Critically Endangered, Rûens Silcrete Renosterveld in the Buffeljagsrivier area, Swellendam by Johannes Philippus Groenewald Thesis presented in fulfilment of the requirements for the degree of Masters in Science in Conservation Ecology in the Faculty of AgriSciences at Stellenbosch University Supervisor: Prof. Michael J. Samways Co-supervisor: Dr. Ruan Veldtman December 2014 Stellenbosch University http://scholar.sun.ac.za Declaration I hereby declare that the work contained in this thesis, for the degree of Master of Science in Conservation Ecology, is my own work that have not been previously published in full or in part at any other University. All work that are not my own, are acknowledge in the thesis. ___________________ Date: ____________ Groenewald J.P. Copyright © 2014 Stellenbosch University All rights reserved ii Stellenbosch University http://scholar.sun.ac.za Acknowledgements Firstly I want to thank my supervisor Prof. M. J. Samways for his guidance and patience through the years and my co-supervisor Dr. R. Veldtman for his help the past few years. This project would not have been possible without the help of Prof. H. Geertsema, who helped me with the identification of the Lepidoptera and other insect caught in the study area. Also want to thank Dr. K. Oberlander for the help with the identification of the Oxalis species found in the study area and Flora Cameron from CREW with the identification of some of the special plants growing in the area. I further express my gratitude to Dr. Odette Curtis from the Overberg Renosterveld Project, who helped with the identification of the rare species found in the study area as well as information about grazing and burning of Renosterveld. -
Project Update: June 2013 the Monte Iberia Plateau at The
Project Update: June 2013 The Monte Iberia plateau at the Alejandro de Humboldt National Park (AHNP) was visited in April and June of 2013. A total of 152 butterflies and moths grouped in 22 families were recorded. In total, 31 species of butterflies belonging to five families were observed, all but two new records to area (see list below). Six species and 12 subspecies are Cuban endemics, including five endemics restricted to the Nipe-Sagua- Baracoa. In total, 108 species of moths belonging to 17 families were registered, including 25 endemic species of which five inhabit exclusively the NSB Mountains (see list below). In total, 52 butterflies and endemic moth species were photographed to be included in a guide of butterflies and endemic moths inhabiting Monte Iberia. Vegetation types sampled were the evergreen forests, rainforest, and charrascals (scrub on serpentine soil) at both north and southern slopes of Monte Iberia plateau Sixteen butterfly species were observed in transects. Park authorities were contacted in preparation on a workshop to capacitate park staff. Butterfly and moth species recorded at different vegetation types of Monte Iberia plateau in April and June of 2013. Symbols and abbreviations: ***- Nipe-Sagua-Baracoa endemic, **- Cuban endemic species, *- Cuban endemic subspecies, F- species photographed, vegetation types: DV- disturbed vegetation, EF- evergreen forest, RF- rainforest, CH- charrascal. "BUTTERFLIES" PAPILIONIDAE Papilioninae Heraclides pelaus atkinsi *F/EF/RF Heraclides thoas oviedo *F/CH Parides g. gundlachianus **F/EF/RF/CH HESPERIIDAE Hesperiinae Asbolis capucinus F/RF/CH Choranthus radians F/EF/CH Cymaenes tripunctus EF Perichares p. philetes F/CH Pyrginae Burca cubensis ***F/RF/CH Ephyriades arcas philemon F/EF/RF Ephyriades b. -
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. -
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. -
RECORDS of the HAWAII BIOLOGICAL SURVEY for 1994 Part 2: Notes1
1 RECORDS OF THE HAWAII BIOLOGICAL SURVEY FOR 1994 Part 2: Notes1 This is the second of two parts to the Records of the Hawaii Biological Survey for 1994 and contains the notes on Hawaiian species of plants and animals including new state and island records, range extensions, and other information. Larger, more comprehensive treatments and papers describing new taxa are treated in the first part of this volume [Bishop Museum Occasional Papers 41]. New Hawaiian Plant Records. I BARBARA M. HAWLEY & B. LEILANI PYLE (Herbarium Pacificum, Department of Natural Sciences, Bishop Museum, P.O. Box 19000A, Honolulu, Hawaii 96817, USA) Amaranthaceae Achyranthes mutica A. Gray Significance. Considered extinct and previously known from only 2 collections: sup- posedly from Hawaii Island 1779, D. Nelson s.n.; and from Kauai between 1851 and 1855, J. Remy 208 (Wagner et al., 1990, Manual of the Flowering Plants of Hawai‘i, p. 181). Material examined. HAWAII: South Kohala, Keawewai Gulch, 975 m, gulch with pasture and relict Koaie, 10 Nov 1991, T.K. Pratt s.n.; W of Kilohana fork, 1000 m, on sides of dry gulch ca. 20 plants seen above and below falls, 350 °N aspect, 16 Dec 1992, K.R. Wood & S. Perlman 2177 (BISH). Caryophyllaceae Silene lanceolata A. Gray Significance. New island record for Oahu. Distribution in Wagner et al. (1990: 523, loc. cit.) limited to Kauai, Molokai, Hawaii, and Lanai. Several plants were later noted by Steve Perlman and Ken Wood from Makua, Oahu in 1993. Material examined. OAHU: Waianae Range, Ohikilolo Ridge at ca. 700 m elevation, off ridge crest, growing on a vertical rock face, facing northward and generally shaded most of the day but in an open, exposed face, only 1 plant noted, 25 Sep 1992, J. -
Ent18 2 117 121 (Kravchenko Et Al).Pmd
Russian Entomol. J. 18(2): 117121 © RUSSIAN ENTOMOLOGICAL JOURNAL, 2009 The Eariadinae and Chloephorinae (Lepidoptera: Noctuoidea, Nolidae) of Israel: distribution, phenology and ecology Eariadinae è Chloephorinae (Lepidoptera: Noctuoidea, Nolidae) Èçðàèëÿ: ðàñïðåäåëåíèå, ôåíîëîãèÿ è ýêîëîãèÿ V.D. Kravchenko1, Th. Witt2, W. Speidel2, J. Mooser3, A. Junnila4 & G.C. Müller4 Â.Ä. Êðàâ÷åíêî1,Ò. Âèòò2, Â. Øïàéäåëü2, Äæ. Ìîçåð3, Ý. Äæàííèëà4 , Ã.Ê. Ìþëëåð4 1 Department of Zoology, Tel Aviv University, Tel Aviv, Israel. 2 Museum Witt, Tengstr. 33, D-80796 Munich, Germany. 3 Seilerbruecklstr. 23, D-85354 Freising, Germany. 4 Department of Parasitology, Kuvin Centre for the Study of Infectious and Tropical Diseases, The Hebrew University Hadassah- Medical School, Jerusalem, Israel. KEY WORDS: Lepidoptera, Israel, Levant, Nolidae, Eariadinae, Chloephorinae, phenology, ecology, host- plants. ÊËÞ×ÅÂÛÅ ÑËÎÂÀ: Lepidoptera, Èçðàèëü, Ëåâàíò, Nolidae, Eariadinae, Chloephorinae, ôåíîëîãèÿ, ýêîëîãèÿ, êîðìîâûå ðàñòåíèÿ. ABSTRACT: The distribution, flight period and âèä, Microxestis wutzdorffi (Püngeler, 1907), ñîáðàííûé abundance of six Israeli Eariadinae and eight Chloe- 80 ëåò íàçàä, íå îáíàðóæåí çà âðåìÿ ðàáîòû phorinae species (Noctuoidea, Nolidae) are summa- Èçðàèëüñêî-Ãåðìàíñêîãî Ïðîåêòà ïî èçó÷åíèþ Lepi- rized. Seven species are new records for Israel: Earias doptera. Äëÿ âñåõ âèäîâ ïðèâîäÿòñÿ äàííûå ïî biplaga Walker, 1866, Earias cupreoviridis (Walker, ÷èñëåííîñòè, ðàñïðåäåëåíèþ, ôåíîëîãèè è ýêîëîãèè. 1862), Acryophora dentula (Lederer, 1870), Bryophilop- Äëÿ ïÿòè âèäîâ âïåðâûå óêàçàíû êîðìîâûå ðàñòåíèÿ. sis roederi (Standfuss, 1892), Nycteola revayana (Sco- poli, 1772), Nycteola columbana (Turner, 1925) and Nycteola asiatica (Krulikovsky, 1904). Three species, Introduction E. biplaga E. cupreoviridis and N. revayana, are re- corded for the first time from the Levante. Only one The Nolidae is a family that has changed in its species, Microxestis wutzdorffi (Püngeler, 1907), col- coverage several times during the past. -
Bosco Palazzi
SHILAP Revista de Lepidopterología ISSN: 0300-5267 ISSN: 2340-4078 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España Bella, S; Parenzan, P.; Russo, P. Diversity of the Macrolepidoptera from a “Bosco Palazzi” area in a woodland of Quercus trojana Webb., in southeastern Murgia (Apulia region, Italy) (Insecta: Lepidoptera) SHILAP Revista de Lepidopterología, vol. 46, no. 182, 2018, April-June, pp. 315-345 Sociedad Hispano-Luso-Americana de Lepidopterología España Available in: https://www.redalyc.org/articulo.oa?id=45559600012 How to cite Complete issue Scientific Information System Redalyc More information about this article Network of Scientific Journals from Latin America and the Caribbean, Spain and Journal's webpage in redalyc.org Portugal Project academic non-profit, developed under the open access initiative SHILAP Revta. lepid., 46 (182) junio 2018: 315-345 eISSN: 2340-4078 ISSN: 0300-5267 Diversity of the Macrolepidoptera from a “Bosco Palazzi” area in a woodland of Quercus trojana Webb., in southeastern Murgia (Apulia region, Italy) (Insecta: Lepidoptera) S. Bella, P. Parenzan & P. Russo Abstract This study summarises the known records of the Macrolepidoptera species of the “Bosco Palazzi” area near the municipality of Putignano (Apulia region) in the Murgia mountains in southern Italy. The list of species is based on historical bibliographic data along with new material collected by other entomologists in the last few decades. A total of 207 species belonging to the families Cossidae (3 species), Drepanidae (4 species), Lasiocampidae (7 species), Limacodidae (1 species), Saturniidae (2 species), Sphingidae (5 species), Brahmaeidae (1 species), Geometridae (55 species), Notodontidae (5 species), Nolidae (3 species), Euteliidae (1 species), Noctuidae (96 species), and Erebidae (24 species) were identified. -
CHECKLIST of WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea)
WISCONSIN ENTOMOLOGICAL SOCIETY SPECIAL PUBLICATION No. 6 JUNE 2018 CHECKLIST OF WISCONSIN MOTHS (Superfamilies Mimallonoidea, Drepanoidea, Lasiocampoidea, Bombycoidea, Geometroidea, and Noctuoidea) Leslie A. Ferge,1 George J. Balogh2 and Kyle E. Johnson3 ABSTRACT A total of 1284 species representing the thirteen families comprising the present checklist have been documented in Wisconsin, including 293 species of Geometridae, 252 species of Erebidae and 584 species of Noctuidae. Distributions are summarized using the six major natural divisions of Wisconsin; adult flight periods and statuses within the state are also reported. Examples of Wisconsin’s diverse native habitat types in each of the natural divisions have been systematically inventoried, and species associated with specialized habitats such as peatland, prairie, barrens and dunes are listed. INTRODUCTION This list is an updated version of the Wisconsin moth checklist by Ferge & Balogh (2000). A considerable amount of new information from has been accumulated in the 18 years since that initial publication. Over sixty species have been added, bringing the total to 1284 in the thirteen families comprising this checklist. These families are estimated to comprise approximately one-half of the state’s total moth fauna. Historical records of Wisconsin moths are relatively meager. Checklists including Wisconsin moths were compiled by Hoy (1883), Rauterberg (1900), Fernekes (1906) and Muttkowski (1907). Hoy's list was restricted to Racine County, the others to Milwaukee County. Records from these publications are of historical interest, but unfortunately few verifiable voucher specimens exist. Unverifiable identifications and minimal label data associated with older museum specimens limit the usefulness of this information. Covell (1970) compiled records of 222 Geometridae species, based on his examination of specimens representing at least 30 counties. -
Influence of Habitat and Bat Activity on Moth Community Composition and Seasonal Phenology Across Habitat Types
INFLUENCE OF HABITAT AND BAT ACTIVITY ON MOTH COMMUNITY COMPOSITION AND SEASONAL PHENOLOGY ACROSS HABITAT TYPES BY MATTHEW SAFFORD THESIS Submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology in the Graduate College of the University of Illinois at Urbana-Champaign, 2018 Urbana, Illinois Advisor: Assistant Professor Alexandra Harmon-Threatt, Chair and Director of Research ABSTRACT Understanding the factors that influence moth diversity and abundance is important for monitoring moth biodiversity and developing conservation strategies. Studies of moth habitat use have primarily focused on access to host plants used by specific moth species. How vegetation structure influences moth communities within and between habitats and mediates the activity of insectivorous bats is understudied. Previous research into the impact of bat activity on moths has primarily focused on interactions in a single habitat type or a single moth species of interest, leaving a large knowledge gap on how habitat structure and bat activity influence the composition of moth communities across habitat types. I conducted monthly surveys at sites in two habitat types, restoration prairie and forest. Moths were collected using black light bucket traps and identified to species. Bat echolocation calls were recorded using ultrasonic detectors and classified into phonic groups to understand how moth community responds to the presence of these predators. Plant diversity and habitat structure variables, including tree diameter at breast height, ground cover, and vegetation height were measured during summer surveys to document how differences in habitat structure between and within habitats influences moth diversity. I found that moth communities vary significantly between habitat types. -
Y Nycteola Columbana (Turner, 1925), Nolidae (Lepidoptera: Noctuoidea) Nuevos Para La Fauna De Asturias (España)
Boletín de la Sociedad Entomológica Aragonesa (S.E.A.), nº 59 (31/12/2016): 281–282. ISSN: 1134-9064 NOTAS CIENTÍFICAS Nola confusalis (Herrich-Schäffer, 1847), Pseudoips prasinana (Linnaeus, 1758) y Nycteola columbana (Turner, 1925), Nolidae (Lepidoptera: Noctuoidea) nuevos para la fauna de Asturias (España) Juan José Guerrero, Rosa María Rubio, Manuel Garre & Antonio S. Ortiz Departamento de Zoología y Antropología Física. Área de Biología Animal. Facultad de Veterinaria, Universidad de Murcia. Cam- pus de Espinardo. 30071 Murcia (España). [email protected] Resumen: Se aportan al catálogo lepidopterológico de Asturias datos sobre cuatro especies de la familia Nolidae (Noctuoidea). Los taxones que se citan por primera vez en el área de estudio son Nola confusalis (Herrich-Schäffer, 1847), Pseudoips prasinana (Linnaeus, 1758) y Nycteola columbana (Turner, 1925), además de confirmar la presencia de Bena bicolorana (Fuessly, 1775). Palabras clave: Insecta, Lepidoptera, Nolidae, nuevas citas, España, Asturias. Nola confusalis (Herrich-Schäffer, 1847), Pseudoips prasinana (Linnaeus, 1758) y Nycteola columbana (Turner, 1925), Nolidae (Lepidoptera: Noctuoidea) new records for Lepidopteran checklist of Asturias (España) Abstract: Nola confusalis (Herrich-Schäffer, 1847), Pseudoips prasinana (Linnaeus, 1758) and Nycteola columbana (Turner, 1925) species belonging to the family Nolidae are reported to the Lepidopteran checklist of Asturias while Bena bicolorana (Fuessly, 1775) is confirmed in the study area. Key words: Insecta, Lepidoptera, Nolidae, new records, Spain, Asturias. Introducción Material y métodos La familia Nolidae Meyrick, 1862 se encuentra representada en la Las capturas se realizaron en el Parque Nacional de Picos de Europa Península Ibérica por 27 especies, de las que once pertenecen al y en el Parque Natural de Somiedo, con trampas de luz negra y actí- género Nola Leach, 1815, y el resto se reparten entre los géneros nica de 15 vatios (tipo Heath), como parte de los muestreos realizados Meganola, Bena, Pseudoips, Nycteola, Garella y Earias (Vives, 2014). -
Lepidoptera: Noctuoidea: Erebidae) and Its Phylogenetic Implications
EUROPEAN JOURNAL OF ENTOMOLOGYENTOMOLOGY ISSN (online): 1802-8829 Eur. J. Entomol. 113: 558–570, 2016 http://www.eje.cz doi: 10.14411/eje.2016.076 ORIGINAL ARTICLE Characterization of the complete mitochondrial genome of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) and its phylogenetic implications YU SUN, SEN TIAN, CEN QIAN, YU-XUAN SUN, MUHAMMAD N. ABBAS, SAIMA KAUSAR, LEI WANG, GUOQING WEI, BAO-JIAN ZHU * and CHAO-LIANG LIU * College of Life Sciences, Anhui Agricultural University, 130 Changjiang West Road, Hefei, 230036, China; e-mails: [email protected] (Y. Sun), [email protected] (S. Tian), [email protected] (C. Qian), [email protected] (Y.-X. Sun), [email protected] (M.-N. Abbas), [email protected] (S. Kausar), [email protected] (L. Wang), [email protected] (G.-Q. Wei), [email protected] (B.-J. Zhu), [email protected] (C.-L. Liu) Key words. Lepidoptera, Noctuoidea, Erebidae, Spilarctia robusta, phylogenetic analyses, mitogenome, evolution, gene rearrangement Abstract. The complete mitochondrial genome (mitogenome) of Spilarctia robusta (Lepidoptera: Noctuoidea: Erebidae) was se- quenced and analyzed. The circular mitogenome is made up of 15,447 base pairs (bp). It contains a set of 37 genes, with the gene complement and order similar to that of other lepidopterans. The 12 protein coding genes (PCGs) have a typical mitochondrial start codon (ATN codons), whereas cytochrome c oxidase subunit 1 (cox1) gene utilizes unusually the CAG codon as documented for other lepidopteran mitogenomes. Four of the 13 PCGs have incomplete termination codons, the cox1, nad4 and nad6 with a single T, but cox2 has TA. It comprises six major intergenic spacers, with the exception of the A+T-rich region, spanning at least 10 bp in the mitogenome.