Butterflies and Moths Are Second Only to Beetles As the Largest Group of Animals in the World
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SYSTEMATICS of the MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of T
SYSTEMATICS OF THE MEGADIVERSE SUPERFAMILY GELECHIOIDEA (INSECTA: LEPIDOPTEA) DISSERTATION Presented in Partial Fulfillment of the Requirements for The Degree of Doctor of Philosophy in the Graduate School of The Ohio State University By Sibyl Rae Bucheli, M.S. ***** The Ohio State University 2005 Dissertation Committee: Approved by Dr. John W. Wenzel, Advisor Dr. Daniel Herms Dr. Hans Klompen _________________________________ Dr. Steven C. Passoa Advisor Graduate Program in Entomology ABSTRACT The phylogenetics, systematics, taxonomy, and biology of Gelechioidea (Insecta: Lepidoptera) are investigated. This superfamily is probably the second largest in all of Lepidoptera, and it remains one of the least well known. Taxonomy of Gelechioidea has been unstable historically, and definitions vary at the family and subfamily levels. In Chapters Two and Three, I review the taxonomy of Gelechioidea and characters that have been important, with attention to what characters or terms were used by different authors. I revise the coding of characters that are already in the literature, and provide new data as well. Chapter Four provides the first phylogenetic analysis of Gelechioidea to include molecular data. I combine novel DNA sequence data from Cytochrome oxidase I and II with morphological matrices for exemplar species. The results challenge current concepts of Gelechioidea, suggesting that traditional morphological characters that have united taxa may not be homologous structures and are in need of further investigation. Resolution of this problem will require more detailed analysis and more thorough characterization of certain lineages. To begin this task, I conduct in Chapter Five an in- depth study of morphological evolution, host-plant selection, and geographical distribution of a medium-sized genus Depressaria Haworth (Depressariinae), larvae of ii which generally feed on plants in the families Asteraceae and Apiaceae. -
A New Macrolepidopteran Moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican Amber
ZooKeys 965: 73–84 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.965.54461 RESEARCH ARTICLE https://zookeys.pensoft.net Launched to accelerate biodiversity research A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber Weiting Zhang1,2, Chungkun Shih3,4, YuHong Shih5, Dong Ren3 1 Hebei GEO University, 136 Huaiandonglu, Shijiazhuang 050031, China 2 State Key Laboratory of Pal- aeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, CAS, Nanjing 210008, China 3 College of Life Sciences and Academy for Multidisciplinary Studies, Capital Normal University, 105 Xisan- huanbeilu, Haidian District, Beijing 100048, China 4 Department of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, USA 5 Laboratorio Dominicano De Ambar Y Gemas, Santo Domingo, Dominican Republic Corresponding author: Weiting Zhang ([email protected]) Academic editor: Gunnar Brehm | Received 19 May 2020 | Accepted 12 August 2020 | Published 3 September 2020 http://zoobank.org/05E273DB-B590-42D1-8234-864A787BE6A0 Citation: Zhang W, Shih C, Shih YH, Ren D (2020) A new macrolepidopteran moth (Insecta, Lepidoptera, Geometridae) in Miocene Dominican amber. ZooKeys 965: 73–84. https://doi.org/10.3897/zookeys.965.54461 Abstract A new genus and species of fossil moth, Miogeometrida chunjenshihi Zhang, Shih & Shih, gen. et sp. nov., assigned to Geometridae, is described from Miocene Dominican amber dating from 15–20 Mya. The new genus is characterized by the forewing without a fovea, R1 not anastomosing with Sc, no areole formed by veins R1 and Rs, R1 and Rs1 completely coincident, M2 arising midway between M1 and M3, anal veins 1A and 2A fused for their entire lengths; and the hind wing with Rs running close to Sc + R1 and M2 absent. -
Western Ghats), Idukki District, Kerala, India
International Journal of Entomology Research International Journal of Entomology Research ISSN: 2455-4758 Impact Factor: RJIF 5.24 www.entomologyjournals.com Volume 3; Issue 2; March 2018; Page No. 114-120 The moths (Lepidoptera: Heterocera) of vagamon hills (Western Ghats), Idukki district, Kerala, India Pratheesh Mathew, Sekar Anand, Kuppusamy Sivasankaran, Savarimuthu Ignacimuthu* Entomology Research Institute, Loyola College, University of Madras, Chennai, Tamil Nadu, India Abstract The present study was conducted at Vagamon hill station to evaluate the biodiversity of moths. During the present study, a total of 675 moth specimens were collected from the study area which represented 112 species from 16 families and eight super families. Though much of the species has been reported earlier from other parts of India, 15 species were first records for the state of Kerala. The highest species richness was shown by the family Erebidae and the least by the families Lasiocampidae, Uraniidae, Notodontidae, Pyralidae, Yponomeutidae, Zygaenidae and Hepialidae with one species each. The results of this preliminary study are promising; it sheds light on the unknown biodiversity of Vagamon hills which needs to be strengthened through comprehensive future surveys. Keywords: fauna, lepidoptera, biodiversity, vagamon, Western Ghats, Kerala 1. Introduction Ghats stretches from 8° N to 22° N. Due to increasing Arthropods are considered as the most successful animal anthropogenic activities the montane grasslands and adjacent group which consists of more than two-third of all animal forests face several threats (Pramod et al. 1997) [20]. With a species on earth. Class Insecta comprise about 90% of tropical wide array of bioclimatic and topographic conditions, the forest biomass (Fatimah & Catherine 2002) [10]. -
New Records of Microlepidoptera in Alberta, Canada
Volume 59 2005 Number 2 Journal of the Lepidopterists’ Society 59(2), 2005, 61-82 NEW RECORDS OF MICROLEPIDOPTERA IN ALBERTA, CANADA GREGORY R. POHL Natural Resources Canada, Canadian Forest Service, Northern Forestry Centre, 5320 - 122 St., Edmonton, Alberta, Canada T6H 3S5 email: [email protected] CHARLES D. BIRD Box 22, Erskine, Alberta, Canada T0C 1G0 email: [email protected] JEAN-FRANÇOIS LANDRY Agriculture & Agri-Food Canada, 960 Carling Ave, Ottawa, Ontario, Canada K1A 0C6 email: [email protected] AND GARY G. ANWEILER E.H. Strickland Entomology Museum, University of Alberta, Edmonton, Alberta, Canada, T6G 2H1 email: [email protected] ABSTRACT. Fifty-seven species of microlepidoptera are reported as new for the Province of Alberta, based primarily on speci- mens in the Northern Forestry Research Collection of the Canadian Forest Service, the University of Alberta Strickland Museum, the Canadian National Collection of Insects, Arachnids, and Nematodes, and the personal collections of the first two authors. These new records are in the families Eriocraniidae, Prodoxidae, Tineidae, Psychidae, Gracillariidae, Ypsolophidae, Plutellidae, Acrolepi- idae, Glyphipterigidae, Elachistidae, Glyphidoceridae, Coleophoridae, Gelechiidae, Xyloryctidae, Sesiidae, Tortricidae, Schrecken- steiniidae, Epermeniidae, Pyralidae, and Crambidae. These records represent the first published report of the families Eriocrani- idae and Glyphidoceridae in Alberta, of Acrolepiidae in western Canada, and of Schreckensteiniidae in Canada. Tetragma gei, Tegeticula -
Insects by Cindy Grigg
Insects By Cindy Grigg 1 Like you, insects are alive. Both people and insects are animals. Insects are different from most other animals. Let's read to find out how they are different. 2 Insects are invertebrate animals. That means they have no backbone. Insects are the largest group of animals on Earth. In fact, about half of all animals that scientists know are insects! 3 Insects have three main body parts. They are the head, the thorax, and the abdomen. They have six legs. Many adult insects also have wings. The wings and legs are attached to the thorax. 4 Some invertebrate animals look like insects, but they are not. Spiders and scorpions, for example, are commonly confused with insects. Spiders and scorpions are not insects because they have eight legs, not six. They also have only two body segments instead of three. 5 Most insects lay eggs. Some young insects look like their parents. Other young insects, such as caterpillars, look very different from their parents. 6 All the stages in the life of an animal make up the animal's life cycle. Butterflies have a four-stage life cycle. Butterflies often lay eggs on leaves the insects can eat after they hatch. The egg is the first stage of the butterfly's life cycle. 7 When the egg hatches, a larva comes out of the egg. We often call the larva a caterpillar. This is the second stage. The caterpillar looks very different from the adult butterfly. The larva eats the leaves and grows very quickly. 8 After the larva grows big enough, it makes a hard covering for itself. -
Bionomics of Bagworms (Lepidoptera: Psychidae)
ANRV363-EN54-11 ARI 27 August 2008 20:44 V I E E W R S I E N C N A D V A Bionomics of Bagworms ∗ (Lepidoptera: Psychidae) Marc Rhainds,1 Donald R. Davis,2 and Peter W. Price3 1Department of Entomology, Purdue University, West Lafayette, Indiana, 47901; email: [email protected] 2Department of Entomology, Smithsonian Institution, Washington D.C., 20013-7012; email: [email protected] 3Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, 86011-5640; email: [email protected] Annu. Rev. Entomol. 2009. 54:209–26 Key Words The Annual Review of Entomology is online at bottom-up effects, flightlessness, mating failure, parthenogeny, ento.annualreviews.org phylogenetic constraint hypothesis, protogyny This article’s doi: 10.1146/annurev.ento.54.110807.090448 Abstract Copyright c 2009 by Annual Reviews. The bagworm family (Lepidoptera: Psychidae) includes approximately All rights reserved 1000 species, all of which complete larval development within a self- 0066-4170/09/0107-0209$20.00 enclosing bag. The family is remarkable in that female aptery occurs in ∗The U.S. Government has the right to retain a over half of the known species and within 9 of the 10 currently recog- nonexclusive, royalty-free license in and to any nized subfamilies. In the more derived subfamilies, several life-history copyright covering this paper. traits are associated with eruptive population dynamics, e.g., neoteny of females, high fecundity, dispersal on silken threads, and high level of polyphagy. Other salient features shared by many species include a short embryonic period, developmental synchrony, sexual segrega- tion of pupation sites, short longevity of adults, male-biased sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case. -
Washington Butterfly Association Common Butterflies of the Puget Sound Region and Their Food Plants
Washington Butterfly Association [email protected] Pine White ( Neophasia menapia ) w ww.naba.org/chapters/nabaws / Identification : White with black forewing patch, black veins below. Flight Period : late June – early October, peak in August. Common Butterflies of the Puget Sound Region Favorite Nectar Plants : Goldenrod, and Their Food Plants - By David Droppers Pearly Everlasting, Asters, Thistles. Larval Host Plants : Ponderosa Pine, Western Tiger Swallowtail ( Papilio Lodgepole Pine, Douglas-Fir, among other conifers. rutulus ). Identification : Large. Yellow with black tiger stripes. Cabbage White ( Pieris rapae) Underside with some blue. Flight Identification : White, black wing tips and Period : mid April – late September, spots. Males have one spot, females two peak in June. Favorite Nectar Plants : spots. Flight Period : early March – early Mock Orange, Milkweeds, Thistles, November, peaks in May, July and large showy flowers. Larval Host September. Favorite Nectar Plants: Plants : Native Willows, Quaking Many, especially garden flowers, such as Oregano and Lavender. Aspen and other poplars, Red Alder Larval Host Plants : Garden Brassicae, especially broccoli and cabbage. Anise Swallowtail ( Papilio zelicaon) Identification : Large. Mostly black, Cedar Hairstreak ( Mitoura grynea ) centrally yellow, with row of blue dots Identification : Small. Varying brown above, below buff brown on hindwing. Flight Period : late with violet tint, variable white postmedian line, small tails on March – late September, peaks in May, hindwings. Flight Period : late March – early August, peaks in July-August. Favorite Nectar Plants : May-June. Favorite Nectar Plants : Goldenrods, Yarrow, Many flowers, mostly large and showy. Dandelion, Clovers, Red Flowering Currant. Larval Host Plants : Garden Parsley Larval Host Plants : Western Red Cedar, Incense Cedar and Dill, Angelica, Cow Parsnip, many others. -
Pest Alert: Box Tree Moth (Cydalima Perspectalis)
Pest Alert Box Tree Moth (Cydalima perspectalis) The box tree moth is an invasive pest that primarily feeds on boxwood species (Buxus spp). In its native range, it also feeds on burning bush (Euonymus alatus), Japanese spindletree (E. japonicus), purple holly (Ilex chinensis), and orange jessamine (Murraya paniculate) once boxwood in the vicinity are completely defoliated. Distribution and Spread The box tree moth is native to temperate and subtropical regions in Asia. It was first reported in Europe in 2007, after which it spread rapidly across European countries and into Western Asia and Northern Africa. In 2018, it was documented in Canada. The rate of spread for the box tree moth has varied since its introduction in Europe, with some cases peaking at 96 miles per year. Long distance movement of the box tree moth across Europe occurred primarily through the movement of infested Adult moths (top and bottom left), damage (bottom) boxwood plantings. Box tree moths are highly mobile and used for edging, as hedges, thick brown border spanning 1.6 and are good fliers. Natural spread and/or clipped into different shapes to 1.8 inches. Some adults have of this moth in Europe is about 3 to make topiaries. The box tree completely brown wings with a small to 6 miles per year. One analysis moth can cause heavy defoliation of white streak on each forewing. Males from Europe concluded that natural boxwood plants if populations are left and females show both colorations. dispersal from continental Europe unchecked. Defoliation of existing to the United Kingdom was possible, and new growth can kill the plant. -
Evolution of the Suctorial Proboscis in Pollen Wasps (Masarinae, Vespidae)
Arthropod Structure & Development 31 (2002) 103–120 www.elsevier.com/locate/asd Evolution of the suctorial proboscis in pollen wasps (Masarinae, Vespidae) Harald W. Krenna,*, Volker Maussb, John Planta aInstitut fu¨r Zoologie, Universita¨t Wien, Althanstraße 14, A-1090, Vienna, Austria bStaatliches Museum fu¨r Naturkunde, Abt. Entomologie, Rosenstein 1, D-70191 Stuttgart, Germany Received 7 May 2002; accepted 17 July 2002 Abstract The morphology and functional anatomy of the mouthparts of pollen wasps (Masarinae, Hymenoptera) are examined by dissection, light microscopy and scanning electron microscopy, supplemented by field observations of flower visiting behavior. This paper focuses on the evolution of the long suctorial proboscis in pollen wasps, which is formed by the glossa, in context with nectar feeding from narrow and deep corolla of flowers. Morphological innovations are described for flower visiting insects, in particular for Masarinae, that are crucial for the production of a long proboscis such as the formation of a closed, air-tight food tube, specializations in the apical intake region, modification of the basal articulation of the glossa, and novel means of retraction, extension and storage of the elongated parts. A cladistic analysis provides a framework to reconstruct the general pathways of proboscis evolution in pollen wasps. The elongation of the proboscis in context with nectar and pollen feeding is discussed for aculeate Hymenoptera. q 2002 Elsevier Science Ltd. All rights reserved. Keywords: Mouthparts; Flower visiting; Functional anatomy; Morphological innovation; Evolution; Cladistics; Hymenoptera 1. Introduction Some have very long proboscides; however, in contrast to bees, the proboscis is formed only by the glossa and, in Evolution of elongate suctorial mouthparts have some species, it is looped back into the prementum when in occurred separately in several lineages of Hymenoptera in repose (Bradley, 1922; Schremmer, 1961; Richards, 1962; association with uptake of floral nectar. -
Biodiversity and Evolution in the Vanilla Genus
1 Biodiversity and Evolution in the Vanilla Genus Gigant Rodolphe1,2, Bory Séverine1,2, Grisoni Michel2 and Besse Pascale1 1University of La Reunion, UMR PVBMT 2CIRAD, UMR PVBMT, France 1. Introduction Since the publication of the first vanilla book by Bouriquet (1954c) and the more recent review on vanilla biodiversity (Bory et al., 2008b), there has been a world regain of interest for this genus, as witnessed by the recently published vanilla books (Cameron, 2011a; Havkin-Frenkel & Belanger, 2011; Odoux & Grisoni, 2010). A large amount of new data regarding the genus biodiversity and its evolution has also been obtained. These will be reviewed in the present paper and new data will also be presented. 2. Biogeography, taxonomy and phylogeny 2.1 Distribution and phylogeography Vanilla Plum. ex Miller is an ancient genus in the Orchidaceae family, Vanilloideae sub- family, Vanilleae tribe and Vanillinae sub-tribe (Cameron, 2004, 2005). Vanilla species are distributed throughout the tropics between the 27th north and south parallels, but are absent in Australia. The genus is most diverse in tropical America (52 species), and can also be found in Africa (14 species) and the Indian ocean islands (10 species), South-East Asia and New Guinea (31 species) and Pacific islands (3 species) (Portères, 1954). From floral morphological observations, Portères (1954) suggested a primary diversification centre of the Vanilla genus in Indo-Malaysia, followed by dispersion on one hand from Asia to Pacific and then America, and on the other hand from Madagascar to Africa. This hypothesis was rejected following the first phylogenetic studies of the genus (Cameron, 1999, 2000) which suggested a different scenario with an American origin of the genus (160 to 120 Mya) and a transcontinental migration of the Vanilla genus before the break-up of Gondwana (Cameron, 2000, 2003, 2005; Cameron et al., 1999). -
Noctuid Moth (Lepidoptera, Noctuidae) Communities in Urban Parks of Warsaw
POLISH ACADEMY OF SCIENCES • INSTITUTE OF ZOOLOGY MEMORABILIA ZOOLOGICA MEMORABILIA ZOOL. 42 125-148 1986 GRAŻYNA WINIARSKA NOCTUID MOTH (LEPIDOPTERA, NOCTUIDAE) COMMUNITIES IN URBAN PARKS OF WARSAW ABSTRACT A total of 40 noctuid moth species were recorded in four parks of Warsaw. Respective moth communities consisted of a similar number of species (17—25), but differed in their abundance index (3.5 —7.9). In all the parks, the dominant species were Autographa gamma and Discrestra trifolii. The subdominant species were represented by Acronicta psi, Trachea atriplicis, Mamestra suasa, Mythimna pallens, and Catocala nupta. There were differences in the species composition and dominance structure among noctuid moth communities in urban parks, suburban linden- oak-hornbeam forest, and natural linden-oak-hornbeam forest. In the suburban and natural linden-oak-hornbeam forests, the number of species was higher by 40% and their abundance wao 5 — 9 times higher than in the urban parks. The species predominating in parks occurred in very low numbers in suburban and natural habitats. Only T. atriplicis belonged to the group of most abundant species in all the habitats under study. INTRODUCTION In recent years, the interest of ecologists in urban habitats has been increasing as they proved to be rich in plant and animal species. The vegetation of urban green areas is sufficiently well known since its species composition and spatial structure are shaped by gardening treatment. But the fauna of these areas is poorly known, and regular zoological investigations in urban green areas were started not so long ago, when urban green was recognized as one of the most important factors of the urban “natural” habitat (Ciborowski 1976). -
Chapter 02 Biogeography and Evolution in the Tropics
Chapter 02 Biogeography and Evolution in the Tropics (a) (b) PLATE 2-1 (a) Coquerel’s Sifaka (Propithecus coquereli), a lemur species common to low-elevation, dry deciduous forests in Madagascar. (b) Ring-tailed lemurs (Lemur catta) are highly social. PowerPoint Tips (Refer to the Microsoft Help feature for specific questions about PowerPoint. Copyright The Princeton University Press. Permission required for reproduction or display. FIGURE 2-1 This map shows the major biogeographic regions of the world. Each is distinct from the others because each has various endemic groups of plants and animals. FIGURE 2-2 Wallace’s Line was originally developed by Alfred Russel Wallace based on the distribution of animal groups. Those typical of tropical Asia occur on the west side of the line; those typical of Australia and New Guinea occur on the east side of the line. FIGURE 2-3 Examples of animals found on either side of Wallace’s Line. West of the line, nearer tropical Asia, one 3 nds species such as (a) proboscis monkey (Nasalis larvatus), (b) 3 ying lizard (Draco sp.), (c) Bornean bristlehead (Pityriasis gymnocephala). East of the line one 3 nds such species as (d) yellow-crested cockatoo (Cacatua sulphurea), (e) various tree kangaroos (Dendrolagus sp.), and (f) spotted cuscus (Spilocuscus maculates). Some of these species are either threatened or endangered. PLATE 2-2 These vertebrate animals are each endemic to the Galápagos Islands, but each traces its ancestry to animals living in South America. (a) and (b) Galápagos tortoise (Geochelone nigra). These two images show (a) a saddle-shelled tortoise and (b) a dome-shelled tortoise.