The Pupae of the Lepidoptera
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Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
Insect Survey of Four Longleaf Pine Preserves
A SURVEY OF THE MOTHS, BUTTERFLIES, AND GRASSHOPPERS OF FOUR NATURE CONSERVANCY PRESERVES IN SOUTHEASTERN NORTH CAROLINA Stephen P. Hall and Dale F. Schweitzer November 15, 1993 ABSTRACT Moths, butterflies, and grasshoppers were surveyed within four longleaf pine preserves owned by the North Carolina Nature Conservancy during the growing season of 1991 and 1992. Over 7,000 specimens (either collected or seen in the field) were identified, representing 512 different species and 28 families. Forty-one of these we consider to be distinctive of the two fire- maintained communities principally under investigation, the longleaf pine savannas and flatwoods. An additional 14 species we consider distinctive of the pocosins that occur in close association with the savannas and flatwoods. Twenty nine species appear to be rare enough to be included on the list of elements monitored by the North Carolina Natural Heritage Program (eight others in this category have been reported from one of these sites, the Green Swamp, but were not observed in this study). Two of the moths collected, Spartiniphaga carterae and Agrotis buchholzi, are currently candidates for federal listing as Threatened or Endangered species. Another species, Hemipachnobia s. subporphyrea, appears to be endemic to North Carolina and should also be considered for federal candidate status. With few exceptions, even the species that seem to be most closely associated with savannas and flatwoods show few direct defenses against fire, the primary force responsible for maintaining these communities. Instead, the majority of these insects probably survive within this region due to their ability to rapidly re-colonize recently burned areas from small, well-dispersed refugia. -
ISSUE #38, Page 68...72 Pickering + State Coordinators
SOUTHERN LEPIDOPTERISTS’ NEWS VOLUME 38 NO.1 (2016), PG. 67 WHY FLY NOW? PUPA BANKS, APOSEMATISM, AND OTHER FACTORS THAT MAY EXPLAIN OBSERVED MOTH FLIGHT ACTIVITY BY JOHN PICKERING Abstract – This paper addresses factors that affect insect flight activity. It presents a 5-year time series of nightly activity at a site in Clarke County, Georgia for Epimecis hortaria, Tulip-tree Beauty (Geometridae: Ennominae)p Nigetia formosalis, Thin-winged Owlet (Erebidae: Scolecocampinae), and Dryocampa rubicunda, Rosy Maple Moth (Saturniidae: Ceratocampinae). These species exemplify three seasonal flight patterns, here defined as diffuse, synchronized, and complex. I propose that diffuse flight patterns are typical of many cryptic species and that synchronized ones are typical of aposematic species and species restricted by the phenology of their hosts. The complex pattern of D. rubicunda shows variation in when individuals broke pupal diapause and eclosed. Because some insects have pupa banks, similar to seed banks in plants, their observed flights and generations may be decoupled. I caution against using terms such as brood, generation, or voltinism to describe observed seasonal adult activity. Instead, I propose that we use the term flight to describe their activity. _____________________________________ Introduction – Many biotic and abiotic factors interact to affect the seasonal flight activity of moths and our ability to sample them accurately (Tauber et al. 1986p Valtonen et al. 2011). They include processes fundamental to each species’ natural history and life cycle. By what means do they disperse, avoid natural enemies, find mates, lay eggs on or near hosts, avoid natural enemies, and in the grand scheme of things, survive for millions of years beyond the next mega-drought, warming period, and ice age? Science has barely begun to explore the complexity of these questions. -
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. -
Forest Insect and Disease Conditions in the Rocky Mountain Region 1997-1999
Forest Insect and Disease Conditions in the Rocky Mountain Region 1997-1999 United States Renewable Rocky Department of Resources Mountain Agriculture Forest Health Region Management 2 FOREST INSECT AND DISEASE CONDITIONS IN THE ROCKY MOUNTAIN REGION 1997-1999 by The Forest Health Management Staff Edited by Jeri Lyn Harris, Michelle Frank, and Susan Johnson December 2001 USDA Forest Service Rocky Mountain Region Renewable Resources, Forest Health Management P.O. Box 25127 Lakewood, Colorado 80225-5127 Cover: Aerial photograph taken by Robert D. Averill on October 29, 1997, just days after a blowdown event occurred on the Routt National Forest. The picture was taken looking east toward a blowdown area that straddles both the Mt. Zirkel Wilderness and the Routt National Forest. “The U.S. Department of Agriculture (USDA) prohibits discrimination in all its programs and activities on the basis of race, color, national origin, sex, religion, age, disability, political beliefs, sexual orientation, or marital or family status. (Not all prohibited bases apply to all programs.) Persons with disabilities who require alternate means for communication of program information (Braille, large print, audiotape, etc.) should contact USDA’s TARGET Center at (202) 720-2600 (voice and TDD). To file a complaint of discrimination, write USDA Director, Office of Civil Rights, Room 326-W, Whitten Building, 1400 Independence Avenue, SW, Washington, DC 20250-9410 or call (202) 720-5964 (voice and TDD). USDA is an equal opportunity employer.” Maps in this product are reproduced from geospatial information prepared by the U.S. Department of Agriculture, Forest Service. GIS data and product accuracy may vary. -
Impacts of Native and Non-Native Plants on Urban Insect Communities: Are Native Plants Better Than Non-Natives?
Impacts of Native and Non-native plants on Urban Insect Communities: Are Native Plants Better than Non-natives? by Carl Scott Clem A thesis submitted to the Graduate Faculty of Auburn University in partial fulfillment of the requirements for the Degree of Master of Science Auburn, Alabama December 12, 2015 Key Words: native plants, non-native plants, caterpillars, natural enemies, associational interactions, congeneric plants Copyright 2015 by Carl Scott Clem Approved by David Held, Chair, Associate Professor: Department of Entomology and Plant Pathology Charles Ray, Research Fellow: Department of Entomology and Plant Pathology Debbie Folkerts, Assistant Professor: Department of Biological Sciences Robert Boyd, Professor: Department of Biological Sciences Abstract With continued suburban expansion in the southeastern United States, it is increasingly important to understand urbanization and its impacts on sustainability and natural ecosystems. Expansion of suburbia is often coupled with replacement of native plants by alien ornamental plants such as crepe myrtle, Bradford pear, and Japanese maple. Two projects were conducted for this thesis. The purpose of the first project (Chapter 2) was to conduct an analysis of existing larval Lepidoptera and Symphyta hostplant records in the southeastern United States, comparing their species richness on common native and alien woody plants. We found that, in most cases, native plants support more species of eruciform larvae compared to aliens. Alien congener plant species (those in the same genus as native species) supported more species of larvae than alien, non-congeners. Most of the larvae that feed on alien plants are generalist species. However, most of the specialist species feeding on alien plants use congeners of native plants, providing evidence of a spillover, or false spillover, effect. -
Ecography E6940 Stange, E., Ayres, M
Ecography E6940 Stange, E., Ayres, M. P. and Bess, J. A. 2011. Concordant population dynamics of Lepidoptera herbivores in a forest ecosystem. – Ecography 34: xxx–xxx. Supplementary material Appendix 1 Environmental conditions that can create spurious effects on black light trapping of adult Lepidoptera (moths) were very similar between years. 2004–2005 (11 dates) 2005–2006 (15 dates) 2006–2007 (21 dates) t-statistic p t-statistic p t-statistic p Moonlight 0.79 0.45 0.07 0.94 0.32 0.76 Temp 1.11 0.29 1.26 0.23 0.41 0.71 Rainfall 0.34 0.75 1.53 0.15 0.38 0.71 Appendix 2 Results of ANOVAs testing for structure in Lepidoptera population dynamics from seven hypothetical sources (each row of table), with commas used to separate degrees of freedom (DF) for groups from those for error. Asterisks indicate significance at p < 0.05 (not control- ling for family-wide error rates). Analyses were performed for each pair of years separately. 2004–2005 2005–2006 2006–2007 Group definition DF F DF F DF F Family 9,63 1.33 9,70 1.34 9,88 1.29 Subfamily 19,49 1.95* 19,53 0.89 22,70 2.06* Larval season 2,65 3.14* 2,71 0.12 2,82 0.63 Flight season 3,71 2.89* 3,78 0.38 3,96 1.28 Overwinter life stage 2,63 3.14* 2,68 0.04 2,75 0.7 Host category 5,68 0.44 5,74 0.32 5,91 0.69 Preferred host 11,45 0.78 12,48 0.91 12,60 1.35 1 Appendix 3 Correlation among moth abundances [Ln(moths × trap–1 × yr–1 + 1) captured in black light traps at three sites (HB, MS and RP] across four years (2004–2007). -
Illustration Sources
APPENDIX ONE ILLUSTRATION SOURCES REF. CODE ABR Abrams, L. 1923–1960. Illustrated flora of the Pacific states. Stanford University Press, Stanford, CA. ADD Addisonia. 1916–1964. New York Botanical Garden, New York. Reprinted with permission from Addisonia, vol. 18, plate 579, Copyright © 1933, The New York Botanical Garden. ANDAnderson, E. and Woodson, R.E. 1935. The species of Tradescantia indigenous to the United States. Arnold Arboretum of Harvard University, Cambridge, MA. Reprinted with permission of the Arnold Arboretum of Harvard University. ANN Hollingworth A. 2005. Original illustrations. Published herein by the Botanical Research Institute of Texas, Fort Worth. Artist: Anne Hollingworth. ANO Anonymous. 1821. Medical botany. E. Cox and Sons, London. ARM Annual Rep. Missouri Bot. Gard. 1889–1912. Missouri Botanical Garden, St. Louis. BA1 Bailey, L.H. 1914–1917. The standard cyclopedia of horticulture. The Macmillan Company, New York. BA2 Bailey, L.H. and Bailey, E.Z. 1976. Hortus third: A concise dictionary of plants cultivated in the United States and Canada. Revised and expanded by the staff of the Liberty Hyde Bailey Hortorium. Cornell University. Macmillan Publishing Company, New York. Reprinted with permission from William Crepet and the L.H. Bailey Hortorium. Cornell University. BA3 Bailey, L.H. 1900–1902. Cyclopedia of American horticulture. Macmillan Publishing Company, New York. BB2 Britton, N.L. and Brown, A. 1913. An illustrated flora of the northern United States, Canada and the British posses- sions. Charles Scribner’s Sons, New York. BEA Beal, E.O. and Thieret, J.W. 1986. Aquatic and wetland plants of Kentucky. Kentucky Nature Preserves Commission, Frankfort. Reprinted with permission of Kentucky State Nature Preserves Commission. -
Recent Records for Parasitism in Saturniidae (Lepidoptera)
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Nachrichten des Entomologischen Vereins Apollo Jahr/Year: 1984 Band/Volume: 5 Autor(en)/Author(s): Peigler Richard S. Artikel/Article: Recent records for parasitism in Saturniidae 95-105 ©Entomologischer Verein Apollo e.V. Frankfurt am Main; download unter www.zobodat.at Nachr. ent. Ver. Apollo, Frankfurt, N. F., Bd. 5, Heft 4: 95—105 — März 1985 95 Recent records for parasitism in Saturniidae (Lepidoptera) by RICHARD S. PEIGLER Abstract: Numerous records of parasites reared from Saturniidae are given, several of which are previously unpublished host-parasite associations. Records are from several regions of the U.S.A. and Central America, with a few from Hong Kong and one from France. Parasites reported here belong to the dipterous family Tachinidae and the hymenopterous families Ichneumonidae, Braconidae, Chalcididae, Perilampidae, Torymidae, Eupel- midae, and Eulophidae. Neuere Beobachtungen über Parasitismus bei Saturniidae (Lepidoptera) Zusammenfassung:Es werden verschiedene Beobachtungen über Parasiten, die aus Saturniiden gezüchtet wurden, gegeben, von denen einige bisher noch unbekannte Wirt-Parasit-Beziehungen darstellen. Die Beobachtungen stammen aus verschiedenen Regionen der USA und Zentralamerikas, einige aus Hongkong und eine aus Frankreich. Die hier genannten Parasiten gehören zu der Dipterenfamilie Tachinidae und den Hymenopterenfa- milien Ichneumonidae, Braconidae, Chalcididae, Perilampidae, Torymidae, Eupelmidae und Eulophidae. Insbesondere wird auf die Notwendigkeit, alle erreichbaren Nachweise von Parasitismus bei Schmetterlingslarven zu dokumentieren und die Parasiten von entsprechenden Fachleuten bestimmen zu lassen, hingewiesen. Sorgfäl tige Zuchtarbeit ist nötig, um einwandfreie Zuordnung der Parasiten zu ihrem jeweiligen Wirt zu ermöglichen; am besten eignet sich hierfür die Einzelhaltung parasitismusverdächtigter Larven. -
Moth Decline in the Northeastern United States David L
_______________________________________________________________________________________News of the Lepidopterists’ Society Volume 54, Number 2 Conservation Matters: Contributions from the Conservation Committee Moth decline in the Northeastern United States David L. Wagner Ecology and Evolutionary Biology, University of Connecticut, Storrs, CT 06268 [email protected] The matter of moth decline in the Northeast and south- ern Canada, particularly of larger moths, has been of con- cern for a half century (Muller 1968-1979, Hessel 1976, Schweitzer 1988, Goldstein 2010). Below I offer an assess- ment, based on my 23 years in New England. Mine is a prospective piece meant to raise the issue of moth decline to a larger audience—it is a call for study, a research agen- da—offered in the absence of the quantitative data needed to make rigorous species-by-species status assessments. As a caveat to what I outline below, I should add that local, regional, and continental biota changes are the norm and that all animal and plant distributions change through time. Ranges and abundances may, in fact, be inherently much more dynamic than is generally understood. At issue here, is not change, but the rate and nature of changes. Hickory horned devil (Citheronia regalis). Members of the genus Lepidoptera and other herbivores are under considerable Citheronia were among the first moths to disappear from New evolutionary pressures from below and above, fated to be England. The last C. regalis record for the region was Syd in never-ending battles with their hostplants (the bottom- Hessels’s 1956 collection from Washington, CT (Ferguson, 1971). up forces) and natural enemies (the top-down forces). -
Appendix 5: Fauna Known to Occur on Fort Drum
Appendix 5: Fauna Known to Occur on Fort Drum LIST OF FAUNA KNOWN TO OCCUR ON FORT DRUM as of January 2017. Federally listed species are noted with FT (Federal Threatened) and FE (Federal Endangered); state listed species are noted with SSC (Species of Special Concern), ST (State Threatened, and SE (State Endangered); introduced species are noted with I (Introduced). INSECT SPECIES Except where otherwise noted all insect and invertebrate taxonomy based on (1) Arnett, R.H. 2000. American Insects: A Handbook of the Insects of North America North of Mexico, 2nd edition, CRC Press, 1024 pp; (2) Marshall, S.A. 2013. Insects: Their Natural History and Diversity, Firefly Books, Buffalo, NY, 732 pp.; (3) Bugguide.net, 2003-2017, http://www.bugguide.net/node/view/15740, Iowa State University. ORDER EPHEMEROPTERA--Mayflies Taxonomy based on (1) Peckarsky, B.L., P.R. Fraissinet, M.A. Penton, and D.J. Conklin Jr. 1990. Freshwater Macroinvertebrates of Northeastern North America. Cornell University Press. 456 pp; (2) Merritt, R.W., K.W. Cummins, and M.B. Berg 2008. An Introduction to the Aquatic Insects of North America, 4th Edition. Kendall Hunt Publishing. 1158 pp. FAMILY LEPTOPHLEBIIDAE—Pronggillled Mayflies FAMILY BAETIDAE—Small Minnow Mayflies Habrophleboides sp. Acentrella sp. Habrophlebia sp. Acerpenna sp. Leptophlebia sp. Baetis sp. Paraleptophlebia sp. Callibaetis sp. Centroptilum sp. FAMILY CAENIDAE—Small Squaregilled Mayflies Diphetor sp. Brachycercus sp. Heterocloeon sp. Caenis sp. Paracloeodes sp. Plauditus sp. FAMILY EPHEMERELLIDAE—Spiny Crawler Procloeon sp. Mayflies Pseudocentroptiloides sp. Caurinella sp. Pseudocloeon sp. Drunela sp. Ephemerella sp. FAMILY METRETOPODIDAE—Cleftfooted Minnow Eurylophella sp. Mayflies Serratella sp. -
Scale Insects
Scale Insects Overview: Scale insects are some of the most destructive pests of shade trees and ornamentals, but few are serious forest pests. All scale insects pierce plant tissues and obtain nutrients by the ingestion of large amounts of plant sap. Localized injury may occur around feeding sites and serious damage or death may occur in heavily infested trees. All adult scales produce a waxy or shell-like covering. Many scale insects are often very inconspicuous (some scale coverings act as camouflage) making diagnosis of an infestation difficult (Fig 5). Others may produce an obvious waxy coating that is easily visible. There are hundreds of species of scale insects that feed on North Carolina trees and shrubs. However, each scale species usually infests only one (or a few) host species. Therefore, many scales are named for the specific host species on which they feed. Causal Agent: Scale insects: Order Hemiptera, Suborder Sternorryncha, Superfamily Coccoidea Hosts: Many species of conifers and hardwoods. Scale insects are usually very host specific. Symptoms / Signs: Symptoms vary widely with the scale species, host, and host tissue attacked. The most common symptoms observed may include foliage spotting, speckling, chlorosis, curling, and/or wilting; as well as galls, distorted growth patterns, bark swelling, twig dieback, branch dieback, decline, and mortality. Adult females are sedentary, wingless, and may lack distinctive divisions between the head, thorax, and 1 abdomen. They are covered with a hard scale or waxy secretion, and can range from /50 inch to ¼ inch long. Scale coverings can be flattened and shield-like (Fig. 3), spherical (Fig.