Orangestriped Oakworm Anisota Senatoria, Saturniidae
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Read Book the Butterfly Ebook
THE BUTTERFLY PDF, EPUB, EBOOK Patricia Polacco | 48 pages | 02 May 2009 | Penguin Putnam Inc | 9780142413067 | English | New York, United States The Butterfly PDF Book I've got to get to work, man! Episode 8 The Job. Episode 1 The Kids. Internally, most of the body cavity is taken up by the gut, but there may also be large silk glands, and special glands which secrete distasteful or toxic substances. Geological Society of America. He ends up hurting himself, and Alison calls the Elmore help desk. According to Lafcadio Hearn , a butterfly was seen in Japan as the personification of a person's soul; whether they be living, dying, or already dead. Just this morning, I pat my son on the head. Very sweet and endearing. Bibcode : Natur. The Hobo : Thank you, sir. Rocky : Uh… Alison : I was so depressed I couldn't get work. Note: division Monotrysia is not a clade. Episode 18 The Wicked. After a butterfly emerges from its chrysalis, Gumball and Darwin release it, and it wreaks havoc all over Elmore. Acanthopteroctetoidea Acanthopteroctetidae archaic sun moths. Bibcode : Sci When the butterfly from earlier lands on one of their heads, the other tries to smack it off but instead punches his friend to a wall. This article is about the Season 3 episode. Episode 38 The List. Coming back to say hello. The Butterfly Writer This is viscous and darkens when exposed to air, becoming a water-insoluble, rubbery material which soon sets solid. Episode 12 The Words. Episode 18 The Refund. Lasiocampidae eggars, snout moths, or lappet moths. -
Manitoba Oakworm Moth
Manitoba Oakworm Moth because of their limited dispersal ability, and its larval preference for younger Bur Oak. This species may actually be Threatened, but data are currently insufficient to assess whether it meets thresholds for status criteria. Wildlife Species Description and e n n e Significance H n o D © : o Manitoba Oakworm Moth (Anisota manitobensis) t o h P is a medium-sized moth (forewing length 19-30 mm) in the family Saturniidae (silk worm moths). Scientific name There are four life stages and the species grows Anisota manitobensis through complete metamorphosis. Adults are brownish-orange, and females are typically Taxon pinker than darker males. The flattened, ovate Arthropods eggs are smooth and yellow, turning to brownish COSEWIC status with age. Larvae are typically dark brown to black Special Concern with paler stripes (tending to pink in later instars) with spines and thoracic horns. Pupae are brown Canadian range and approximately 3 cm long. Manitoba Reason for designation Distribution This large moth has a small global distribution, The known global and Canadian range of most of which is in Canada, and restricted to a Manitoba Oakworm Moth is restricted to southern small area in southern Manitoba and the adjacent Manitoba and extreme northern North Dakota United States. Localized population irruptions and Minnesota. The majority of the global range occurred irregularly through the 1900s, but their is in Manitoba where it has been recorded from frequency declined and the last one was in 1997; approximately 25 sites as far north as Riding no individuals have been detected since 2000. Mountain National Park. -
GIS Handbook Appendices
Aerial Survey GIS Handbook Appendix D Revised 11/19/2007 Appendix D Cooperating Agency Codes The following table lists the aerial survey cooperating agencies and codes to be used in the agency1, agency2, agency3 fields of the flown/not flown coverages. The contents of this list is available in digital form (.dbf) at the following website: http://www.fs.fed.us/foresthealth/publications/id/id_guidelines.html 28 Aerial Survey GIS Handbook Appendix D Revised 11/19/2007 Code Agency Name AFC Alabama Forestry Commission ADNR Alaska Department of Natural Resources AZFH Arizona Forest Health Program, University of Arizona AZS Arizona State Land Department ARFC Arkansas Forestry Commission CDF California Department of Forestry CSFS Colorado State Forest Service CTAES Connecticut Agricultural Experiment Station DEDA Delaware Department of Agriculture FDOF Florida Division of Forestry FTA Fort Apache Indian Reservation GFC Georgia Forestry Commission HOA Hopi Indian Reservation IDL Idaho Department of Lands INDNR Indiana Department of Natural Resources IADNR Iowa Department of Natural Resources KDF Kentucky Division of Forestry LDAF Louisiana Department of Agriculture and Forestry MEFS Maine Forest Service MDDA Maryland Department of Agriculture MADCR Massachusetts Department of Conservation and Recreation MIDNR Michigan Department of Natural Resources MNDNR Minnesota Department of Natural Resources MFC Mississippi Forestry Commission MODC Missouri Department of Conservation NAO Navajo Area Indian Reservation NDCNR Nevada Department of Conservation -
Larval Protein Quality of Six Species of Lepidoptera (Saturniidaeo Sphingidae, Noctuidae)
Larval Protein Quality of Six Species of Lepidoptera (Saturniidaeo Sphingidae, Noctuidae) STEPHEN V. LANDRY,I GENE R. DEFOLIART,IANP MILTON L. SUNDE, University of Wisconsin, Madison, Wisconsin 53706 J. Econ. Entomol. 79; 600-604 (I98€) ABSTRACT Six lepidopteran species representing three families were evaluated for their potential use as protein supplements for poultry. Proximate and amino acid analyses were conducted on larval powders of each species. Larvae ranged from 49.4 to 58.1% crude protein on a dry-weight basis. Amino acid analysis indicated deficiencies in arginine, me- thionine, cysteine, and possibly lysine, when larvae are used in chick rations. In a chick- feeding trial with three of the species, however, these deffciencies were not substantiated: the average weight gained by chicks fed the lepidopteran-supplemented dlet did not differ significantly from that of.chicks fed a conventional corn/soybean control diet. LnprpoptBne ARE among the many species of in- by feeding trials on poultry (Ichhponani and Ma- sects that have played an important role in nutri- Iek 1971, Wijayasinghe and Rajaguru 1977). tion, especially in areas where human and domes- To determine and compare the protein quality tic animal populations are subject to chronic protein of a wider assortment of lepidopterous larvae, we deficiency (e.g., Bodenheimer 1951, Quin 1959, conducted proximate and amino acid analyses on Ruddle 1973, Conconi and Bourges 1977, Malaise larvae of six species representing three families. and Parent 1980, Conconi et al. 1984). Conconi et These included the cecropia moth, Hgalophora ce- al. (f9Sa), for example, listed 12 species in 8 fam- cropia (L.), and the promethea moth, Callosamia ilies that are gathered and consumed in Mexico. -
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. -
First Record of Citheronia Regalis (Lepidoptera: Saturniidae) Feeding on Cotinus Obovatus (Anacardiaceae) Author(S): Gary R
First Record of Citheronia regalis (Lepidoptera: Saturniidae) Feeding on Cotinus obovatus (Anacardiaceae) Author(s): Gary R. Graves Source: Florida Entomologist, 100(2):474-475. Published By: Florida Entomological Society https://doi.org/10.1653/024.100.0210 URL: http://www.bioone.org/doi/full/10.1653/024.100.0210 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Scientific Notes First record of Citheronia regalis (Lepidoptera: Saturniidae) feeding on Cotinus obovatus (Anacardiaceae) Gary R. Graves1,2,* The regal moth (Citheronia regalis F.; Lepidoptera: Saturniidae) 2016) shows historic and recent records of C. regalis for only 11 of was historically distributed in eastern North America from southern the 34 counties in which natural populations of smoketree have been New England and southern Michigan, south to southern Florida, and documented (Davis & Graves 2016). west to eastern Nebraska and eastern Texas (Tuskes et al. -
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. -
Colourful Butterfly Wings: Scale Stacks, Iridescence and Sexual Dichromatism of Pieridae Doekele G
158 entomologische berichten 67(5) 2007 Colourful butterfly wings: scale stacks, iridescence and sexual dichromatism of Pieridae Doekele G. Stavenga Hein L. Leertouwer KEY WORDS Coliadinae, Pierinae, scattering, pterins Entomologische Berichten 67 (5): 158-164 The colour of butterflies is determined by the optical properties of their wing scales. The main scale structures, ridges and crossribs, scatter incident light. The scales of pierid butterflies have usually numerous pigmented beads, which absorb light at short wavelengths and enhance light scattering at long wavelengths. Males of many species of the pierid subfamily Coliadinae have ultraviolet-iridescent wings, because the scale ridges are structured into a multilayer reflector. The iridescence is combined with a yellow or orange-brown colouration, causing the common name of the subfamily, the yellows or sulfurs. In the subfamily Pierinae, iridescent wing tips are encountered in the males of most species of the Colotis-group and some species of the tribe Anthocharidini. The wing tips contain pigments absorbing short-wavelength light, resulting in yellow, orange or red colours. Iridescent wings are not found among the Pierini. The different wing colours can be understood from combinations of wavelength-dependent scattering, absorption and iridescence, which are characteristic for the species and sex. Introduction often complex and as yet poorly understood optical phenomena The colour of a butterfly wing depends on the interaction of encountered in lycaenids and papilionids. The Pieridae have light with the material of the wing and its spatial structure. But- two main subfamilies: Coliadinae and Pierinae. Within Pierinae, terfly wings consist of a wing substrate, upon which stacks of the tribes Pierini and Anthocharidini are distinguished, together light-scattering scales are arranged. -
Flexural Stiffness Patterns of Butterfly Wings (Papilionoidea)
35:61–77,Journal of Research1996 (2000) on the Lepidoptera 35:61–77, 1996 (2000) 61 Flexural stiffness patterns of butterfly wings (Papilionoidea) Scott J. Steppan Committee on Evolutionary Biology, University of Chicago, Chicago, IL 60637, USA., E-mail: [email protected] Abstract. A flying insect generates aerodynamic forces through the ac- tive manipulation of the wing and the “passive” properties of deformability and wing shape. To investigate these “passive” properties, the flexural stiffness of dried forewings belonging to 10 butterfly species was compared to the butterflies’ gross morphological parameters to determine allom- etric relationships. The results show that flexural stiffness scales with wing 3.9 loading to nearly the fourth power (pw ) and is highly correlated with wing area cubed (S3.1). The generalized map of flexural stiffness along the wing span for Vanessa cardui has a reduction in stiffness near the distal tip and a large reduction near the base. The distal regions of the wings are stiffer against forces applied to the ventral side, while the basal region is much stiffer against forces applied dorsally. The null hypothesis of structural isom- etry as the explanation for flexural stiffness scaling is rejected. Instead, selection for a consistent dynamic wing geometry (angular deflection) in flight may be a major factor controlling general wing stiffness and deformability. Possible relationships to aerodynamic and flight habit fac- tors are discussed. This study proposes a new approach to addressing the mechanics of insect flight and these preliminary results need to be tested using fresh wings and more thorough sampling. KEY WORDS: biomechanics, butterfly wings, flight, allometry, flexural stiff- ness, aerodynamics INTRODUCTION A flying insect generates aerodynamic forces primarily through the ac- tive manipulation of wing movements and the “passive” morphological prop- erties of deformability and wing shape. -
Moths of Ohio Guide
MOTHS OF OHIO field guide DIVISION OF WILDLIFE This booklet is produced by the ODNR Division of Wildlife as a free publication. This booklet is not for resale. Any unauthorized INTRODUCTION reproduction is prohibited. All images within this booklet are copyrighted by the Division of Wildlife and it’s contributing artists and photographers. For additional information, please call 1-800-WILDLIFE. Text by: David J. Horn Ph.D Moths are one of the most diverse and plentiful HOW TO USE THIS GUIDE groups of insects in Ohio, and the world. An es- Scientific Name timated 160,000 species have thus far been cata- Common Name Group and Family Description: Featured Species logued worldwide, and about 13,000 species have Secondary images 1 Primary Image been found in North America north of Mexico. Secondary images 2 Occurrence We do not yet have a clear picture of the total Size: when at rest number of moth species in Ohio, as new species Visual Index Ohio Distribution are still added annually, but the number of species Current Page Description: Habitat & Host Plant is certainly over 3,000. Although not as popular Credit & Copyright as butterflies, moths are far more numerous than their better known kin. There is at least twenty Compared to many groups of animals, our knowledge of moth distribution is very times the number of species of moths in Ohio as incomplete. Many areas of the state have not been thoroughly surveyed and in some there are butterflies. counties hardly any species have been documented. Accordingly, the distribution maps in this booklet have three levels of shading: 1. -
BRUSH-FOOTED BUTTERFLIES OR FOUR-FOOTED BUTTERFLIES NYMPHALIDAE (RAFINESQUE, 1815) Classification Kingdom
BRUSH-FOOTED BUTTERFLIES OR FOUR-FOOTED BUTTERFLIES NYMPHALIDAE (RAFINESQUE, 1815) NATURAL HISTORY SUMMARY BY JACOB EGGE, PHD Classification Kingdom: Animalia Phylum: Arthropoda Class: Insecta Order: Lepidoptera Family: Nymphalidae Description The family Nymphalidae includes some 6,000 species of butterflies. Most species in this family have greatly reduced forelegs and stand on only four legs. The vestigial forelegs have a brush-like set of hairs. Antennae always have two grooves on the underside. Many have brightly colored wings with cryptic undersides that help provide camouflage among leaves and brush. Familiar species in the family include the Monarch (Danaus plexippus) and fritillaries (Speyeria and Boloria). Distribution The family Nymphalidae has representative species on all continents except Antarctica, but they are most diverse in the Neotropics (DeVries 1987). Diet Nymphalid caterpillars feed exclusively on plants and many are host specific, while others are generalists. Adults generally feed on nectar from flowers they suck through a proboscis. However, some species feed on sap, fermenting fruit, or dung. (Hadley 2016). Habitat and Ecology Nyphalids inhabit a variety of habitats ranging from tropical rainforests to tundra environments of high elevation summits. Many species of Nymphalid, including the Monarch, have distasteful body fluids that deter predators. These distasteful compounds are derived from the plants they feed on as caterpillars. Most species are diurnal, with a few nocturnal species. Caterpillars are typically found associated with a particular host plant species or group of plants. Plant specializations range broadly across the family and include aster, violet, willow, elm, poplar, nettles, thistle, hackberry, and milkweed (Triplehorn and Johnson 2005). Reproduction and Life Cycle All butterflies undergo complete metamorphosis with both a larval (caterpillar) and pupal stage. -
POCKET GUIDE to Common Kansas Butterflies ■ ■ ■ ■ ■
A POCKET GUIDE TO Common Kansas Butterflies ■ ■ ■ ■ ■ By Jim Mason Funded by Westar Energy Green Team, Glenn Springs Holdings, Inc., Occidental Chemical Corporation and the Chickadee Checkoff Published by the Friends of the Great Plains Nature Center Table of Contents • Introduction • 2 • Butterflies vs. Moths • 4 • Observing Butterflies • 4 Family Papilionidae - Swallowtails ■ Pipevine Swallowtail • 6 ■ Zebra Swallowtail • 7 ■ Black Swallowtail • 8 ■ Giant Swallowtail • 9 ■ Eastern Tiger Swallowtail • 10 Family Pieridae – Whites & Sulphurs ■ Checkered White • 11 ■ Cabbage White • 12 ■ Clouded Sulphur • 13 ■ Orange Sulphur • 14 ■ Cloudless Sulphur • 15 ■ Sleepy Orange • 16 ■ Little Yellow • 17 ■ Dainty Sulphur • 18 ■ Southern Dogface • 19 Family Lycaenidae – Gossamer-Wings ■ Gray Copper • 20 ■ Bronze Copper • 21 ■ Coral Hairstreak • 22 ■ Gray Hairstreak • 23 ■ Juniper Hairstreak • 24 ■ Reakirts' Blue • 25 ■ Eastern Tailed-Blue • 26 ■ Spring Azure and Summer Azure • 27 Family Nymphalidae – Brushfoots ■ American Snout • 28 ■ Variegated Fritillary • 29 ■ Great Spangled Fritillary • 30 ■ Regal Fritillary • 31 ■ Gorgone Checkerspot • 32 ■ Silvery Checkerspot • 33 ■ Phaon Crescent • 34 ■ Pearl Crescent • 35 ■ Question Mark • 36 ■ Eastern Comma • 37 ■ Mourning Cloak • 38 ■ American Lady • 39 ©Greg Sievert ■ Painted Lady • 40 ■ Red Admiral • 41 ■ Common Buckeye • 42 ■ Red-spotted Purple • 43 ■ Viceroy • 44 ■ Goatweed Leafwing • 45 ■ Hackberry Emperor • 46 ■ Tawny Emperor • 47 ■ Little Wood Satyr • 48 ■ Common Wood Nymph • 49 ■ Monarch • 50 Family