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Butterflies of Ontario & Summaries of Lepidoptera
ISBN #: 0-921631-12-X BUTTERFLIES OF ONTARIO & SUMMARIES OF LEPIDOPTERA ENCOUNTERED IN ONTARIO IN 1991 BY A.J. HANKS &Q.F. HESS PRODUCTION BY ALAN J. HANKS APRIL 1992 CONTENTS 1. INTRODUCTION PAGE 1 2. WEATHER DURING THE 1991 SEASON 6 3. CORRECTIONS TO PREVIOUS T.E.A. SUMMARIES 7 4. SPECIAL NOTES ON ONTARIO LEPIDOPTERA 8 4.1 The Inornate Ringlet in Middlesex & Lambton Cos. 8 4.2 The Monarch in Ontario 8 4.3 The Status of the Karner Blue & Frosted Elfin in Ontario in 1991 11 4.4 The West Virginia White in Ontario in 1991 11 4.5 Butterfly & Moth Records for Kettle Point 11 4.6 Butterflies in the Hamilton Study Area 12 4.7 Notes & Observations on the Early Hairstreak 15 4.8 A Big Day for Migrants 16 4.9 The Ocola Skipper - New to Ontario & Canada .17 4.10 The Brazilian Skipper - New to Ontario & Canada 19 4.11 Further Notes on the Zarucco Dusky Wing in Ontario 21 4.12 A Range Extension for the Large Marblewing 22 4.13 The Grayling North of Lake Superior 22 4.14 Description of an Aberrant Crescent 23 4.15 A New Foodplant for the Old World Swallowtail 24 4.16 An Owl Moth at Point Pelee 25 4.17 Butterfly Sampling in Algoma District 26 4.18 Record Early Butterfly Dates in 1991 26 4.19 Rearing Notes from Northumberland County 28 5. GENERAL SUMMARY 29 6. 1990 SUMMARY OF ONTARIO BUTTERFLIES, SKIPPERS & MOTHS 32 Hesperiidae 32 Papilionidae 42 Pieridae 44 Lycaenidae 48 Libytheidae 56 Nymphalidae 56 Apaturidae 66 Satyr1dae 66 Danaidae 70 MOTHS 72 CONTINUOUS MOTH CYCLICAL SUMMARY 85 7. -
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, -
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] 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, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11 -
Lepidoptera: Sphingidae) in Michigan
The Great Lakes Entomologist Volume 25 Number 3 - Fall 1992 Number 3 - Fall 1992 Article 8 October 1992 Northerly-Outlying Records of Two Species of Hawkmoths (Lepidoptera: Sphingidae) in Michigan John F. Douglass Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Douglass, John F. 1992. "Northerly-Outlying Records of Two Species of Hawkmoths (Lepidoptera: Sphingidae) in Michigan," The Great Lakes Entomologist, vol 25 (3) Available at: https://scholar.valpo.edu/tgle/vol25/iss3/8 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Douglass: Northerly-Outlying Records of Two Species of Hawkmoths (Lepidopte 1992 THE GREAT LAKES ENTOMOLOGIST 237 NORTHERLY-OUTLYING RECORDS OF TWO SPECIES OF HAWKMOTHS (LEPIDOPTERA: SPHINGIDAE) IN MICHIGAN John F. Douglassl The Grand Traverse Region of Lower Michigan is of special interest zoo geographically in that it includes the northernmost known localities for vari ous species of organisms characteristic of the Carolinian Biotic Province (Douglass 1977, 1983; McCann 1979). On 5 July 1984 I found a gravid female achemon sphinx (Eumorpha ache mon [Drury]) dead on Figg. Rd., Benzie Co. (T26N, R16W, boundary Sec. 14-15, N of jct. Graves Rd.). The specimen (collected) is in fresh condition, and appeared to have been rather freshly killed: greenish eggs had spilled from the ruptured abdomen and were congealing in the sand. -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
Are Pollinating Hawk Moths Declining in the Northeastern United States? an Analysis of Collection Records
11/30/2017 Are pollinating hawk moths declining in the Northeastern United States? An analysis of collection records Are pollinating hawk moths declining in the Northeastern United States? An analysis of collection records Bruce E. Young , Stephanie Auer , Margaret Ormes , Giovanni Rapacciuolo , Dale Schweitzer , Nicole Sears Published: October 5, 2017 https://doi.org/10.1371/journal.pone.0185683 Abstract Increasing attention to pollinators and their role in providing ecosystem services has revealed a paucity of studies on long-term population trends of most insect pollinators in many parts of the world. Because targeted monitoring programs are resource intensive and unlikely to be performed on most insect pollinators, we took advantage of existing collection records to examine long- term trends in northeastern United States populations of 26 species of hawk moths (family Sphingidae) that are presumed to be pollinators. We compiled over 6,600 records from nine museum and 14 private collections that spanned a 112-year period, and used logistic generalized linear mixed models (GLMMs) to examine long-term population trends. We controlled for uneven sampling effort by adding a covariate for list length, the number of species recorded during each sampling event. We found that of the 22 species for which there was sufficient data to assess population trends, eight species declined and four species increased in detection probability (the probability of a species being recorded during each year while accounting for effort, climate, and spatial effects in the GLMMs). Of the four species with too few records to statistically assess, two have disappeared from parts of their ranges. -
Distribution and Phenologies of Louisiana Sphingidae
jO/trnaZ of the Lepidopterists' Society 51(2). 1997. 156-175 DISTRIBUTION AND PHENOLOGIES OF LOUISIANA SPHINGIDAE VERNON ANTOINE BROU, JR. AND CHARLOTTE DOZAR BROU 74.320 Jack Loyd Road, Abita Springs, Louisiana 70420, USA ABSTRACT. The abundance, distribution, and flight periods for 55 species of Louisiana Sphingidae are presented, including plior literature records and new collecting data for 44 species taken over a 26-year period (1970 through 1995). Information is pro vided on the number of annual broods for .36 species, and dates of capture are plotted as one-year and composite graphs for 30 species. Additional key words: bait traps, hawkmoths, light traps, sphinx moths, voltinism. The first treatment of the family Sphingidae in Louisiana was pre sented by von Reizenstein (1863), who reported 33 species from the vicinity of New Orleans. Later, von Reizenstein (1881) and Ottolengui (1894) each tallied one additional species for the state, and subsequent published works during this century have gradually expanded the total by another dozen species (see Rothschild & Jordan 1903, Hine 1906, Clark 1917, Draudt 1931, Jung 1950, Merkl & pfrimmer 1955, pfrim mer 1957, Brou 1980, Covell 1984, Brou 1994). For some time, we have been monitoring and collecting adult Louisiana Sphingidae in order to produce a comprehensive state list and examine voltinism and variation in the abundance of adults from brood to brood. In the present paper, we discuss the results from 26 years of sampling, 1970 through 1995. MATERIALS AND METHODS We used ultraviolet light traps and fermenting bait traps to attract sphingids, logging approximately 416,000 light trap hours and 633,000 bait trap hours from 1970 through 1995. -
Butterflies of North America
Insects of Western North America 7. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. 4. Hexapoda: Selected Coleoptera and Diptera with cumulative list of Arthropoda and additional taxa Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University, Fort Collins, CO 80523-1177 2 Insects of Western North America. 7. Survey of Selected Arthropod Taxa of Fort Sill, Comanche County, Oklahoma. 4. Hexapoda: Selected Coleoptera and Diptera with cumulative list of Arthropoda and additional taxa by Boris C. Kondratieff, Luke Myers, and Whitney S. Cranshaw C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 August 22, 2011 Contributions of the C.P. Gillette Museum of Arthropod Diversity. Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523-1177 3 Cover Photo Credits: Whitney S. Cranshaw. Females of the blow fly Cochliomyia macellaria (Fab.) laying eggs on an animal carcass on Fort Sill, Oklahoma. 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, Colorado, 80523-1177. Copyrighted 2011 4 Contents EXECUTIVE SUMMARY .............................................................................................................7 SUMMARY AND MANAGEMENT CONSIDERATIONS -
1 Modern Threats to the Lepidoptera Fauna in The
MODERN THREATS TO THE LEPIDOPTERA FAUNA IN THE FLORIDA ECOSYSTEM By THOMSON PARIS A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2011 1 2011 Thomson Paris 2 To my mother and father who helped foster my love for butterflies 3 ACKNOWLEDGMENTS First, I thank my family who have provided advice, support, and encouragement throughout this project. I especially thank my sister and brother for helping to feed and label larvae throughout the summer. Second, I thank Hillary Burgess and Fairchild Tropical Gardens, Dr. Jonathan Crane and the University of Florida Tropical Research and Education center Homestead, FL, Elizabeth Golden and Bill Baggs Cape Florida State Park, Leroy Rogers and South Florida Water Management, Marshall and Keith at Mack’s Fish Camp, Susan Casey and Casey’s Corner Nursery, and Michael and EWM Realtors Inc. for giving me access to collect larvae on their land and for their advice and assistance. Third, I thank Ryan Fessendon and Lary Reeves for helping to locate sites to collect larvae and for assisting me to collect larvae. I thank Dr. Marc Minno, Dr. Roxanne Connely, Dr. Charles Covell, Dr. Jaret Daniels for sharing their knowledge, advice, and ideas concerning this project. Fourth, I thank my committee, which included Drs. Thomas Emmel and James Nation, who provided guidance and encouragement throughout my project. Finally, I am grateful to the Chair of my committee and my major advisor, Dr. Andrei Sourakov, for his invaluable counsel, and for serving as a model of excellence of what it means to be a scientist. -
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. -
Plum Island Biodiversity Inventory
Plum Island Biodiversity Inventory New York Natural Heritage Program Plum Island Biodiversity Inventory Established in 1985, the New York Natural Heritage NY Natural Heritage also houses iMapInvasives, an Program (NYNHP) is a program of the State University of online tool for invasive species reporting and data New York College of Environmental Science and Forestry management. (SUNY ESF). Our mission is to facilitate conservation of NY Natural Heritage has developed two notable rare animals, rare plants, and significant ecosystems. We online resources: Conservation Guides include the accomplish this mission by combining thorough field biology, identification, habitat, and management of many inventories, scientific analyses, expert interpretation, and the of New York’s rare species and natural community most comprehensive database on New York's distinctive types; and NY Nature Explorer lists species and biodiversity to deliver the highest quality information for communities in a specified area of interest. natural resource planning, protection, and management. The program is an active participant in the The Program is funded by grants and contracts from NatureServe Network – an international network of government agencies whose missions involve natural biodiversity data centers overseen by a Washington D.C. resource management, private organizations involved in based non-profit organization. There are currently land protection and stewardship, and both government and Natural Heritage Programs or Conservation Data private organizations interested in advancing the Centers in all 50 states and several interstate regions. conservation of biodiversity. There are also 10 programs in Canada, and many NY Natural Heritage is housed within NYS DEC’s participating organizations across 12 Latin and South Division of Fish, Wildlife & Marine Resources. -
Moths of the Kingston Study Area
Moths of the Kingston Study Area Last updated 30 July 2015 by Mike Burrell This checklist contains the 783 species known to have occurred within the Kingston Study. Major data sources include KFN bioblitzes, an earlier version created by Gary Ure (2013) and the Queen’s University Biological Station list by Kit Muma (2008). For information about contributing your sightings or to download the latest version of this checklist, please visit: http://kingstonfieldnaturalists.org/moths/moths.html Contents Superfamily: Tineoidea .................................................................................................................................................... 5 Family: Tineidae ........................................................................................................................................................... 5 Subfamily: Tineinae .................................................................................................................................................. 5 Family: Psychidae ......................................................................................................................................................... 5 Subfamily: Psychinae ................................................................................................................................................ 5 Superfamily: Gracillarioidea ............................................................................................................................................. 5 Family: Gracillariidae ...................................................................................................................................................