The Gtpst and Brown-Tail Moths and Their European Parasites

Total Page:16

File Type:pdf, Size:1020Kb

The Gtpst and Brown-Tail Moths and Their European Parasites THE GTPST AND BROWN-TAIL MOTHS AND THEIR EUROPEAN PARASITES. By L. O. HowABD, Ph. D., Chief of the Bureau of JEntomology. INTRODUCTION AND SPRKaD.OF THE MOTHS IN UNITED STATES. All of the earlier works on the injurious insects of Europe have contained references to and descriptions of the so-called gypsy mpth {Ocne7'ia dispar Linn.). The brown-tail moth (Miprootis chrysorrhœa Linn.) is also a native European insect and for many years has been noted as an enemy to fruit trees. Both of these insects have been introduced into the United States in the vicinity of Boston and have multiplied and spread with alarming i-apidity. The gypsy moth was first introduced in 1868 by Prof. L. Trouvelot, of Harvard University, who was experimenting in the crossbreeding of wild silkworms. An egg cluster of the gypsy moth blew out of his window in Maiden, and he was unable to recover it. Twenty years later, in 1889, the species had increased to such an extent that the cater- pillars were a great nuisance in the city of Maiden, and the State under- took an investigation in the hope of exterminating the species. It was found to have spread until it occupied a territory of about 100 square miles, and during the next ten years the State, by constantly increas- ing appropriations and by the active work of a large number of paid employees, had succeeded in practically controlling all further spread and in greatly reducing the numbers of the insect. In 1900, however, appropriations lapsed, and from that year until 1905 the insect was again allowed to multiply and spread, unhindered save by the opera- tions of private persons. It soon became as numerous as it had been early in the State investigation, and the boundaries of the region inhab- ited by it widened out greatly, until now it has reached as far west as Worcester and occurs all along the New Hampshire line on the north, extending over into that State at Seabrook, Hampton, North Hampton, and Portsmouth (see fig. 1). It has also made its appearance in por- tions of Providence, R. I. The brown-tail moth was first noticed in the early nineties in Somer- ville, Mass., where it was probably introduced in a shipment of roses from Holland. It multiplied and spread, although the work of the gypsy moth commission was directed against this insect as well as against the gypsy moth down to the year 1900. It has since become 123 124 YEARBOOK OF THE DEPARTMENT OF AGRICULTURE. even more abundant and injurious than the gypsy moth, and, owing to the fact that the female flies readily, whereas the female of the gypsy moth does not fly at all, the brown-tail moth has far exceeded the gypsy moth in its spread. It now covers a territory extending from East- port, Me., on the northeast, as far south as Cape Cod, and to the west FIG. 1.—Sketch map of eastern Massachusetts, showing gypsy moth area. as far as Amherst, Mass. It doubtless also exists in many communi- ties in and out of Massachusetts from which it has not been reported. LIFE HISTORY AND DESCRIPTION OF THE GYPSY MOTH. The gypsy moth has but a single generation each year. It winters in the egg stage, and the young caterpillar hatches from the egg about THE GYPSY AJSTD BROWK-TAIL MOTHS. 125 the first of May. It feeds upon the leaves of many different plants. It attacks practically all fruit, shade, and woodland trees, showing some preference for apple, white oak, red oak, willow, and elm. It kills both deciduous and coniferous trees. Woodlands attacked by it in number are stripped bare and many trees are killed. It feeds upon the foliage of shrubs, vines, bushes, and flowers, and will eat grass and garden and field crops. The full-grown caterpillar is 3 inches or a little less in length, and has a dark-gray or sooty color effect. The back is marked with yellow; along the back is a double row of blue spots fol- lowed by a double row of red spots—five pairs of blue and six pairs of red. The young larvae do not show these spots well, but in the full- grown ones they are very evident. About the first of July, or a little later, the larva changes to pupa (PI. I) in a partial cocoon formed of a few FIG. 2.—The gypsy moth {Ocneria dispar): a, female moth; 6, male moth; c, halfgrown larva; d, mature larva. Slightly enlarged (original). türeads of silk, sometimes connecting leaves together. From the mid- dle of July to the middle of August the winged moths appear (fig. 2), The male is brownish yellow, and has a slender body and a wing expanse of about li inches. It is an active flier. The female moth is nearly white, somewhat spotted with black. It is very sluggish, and its body is so heavy that it can not fly. Its wing expanse is about 2i inches. The eggs are deposited by the females shortly after issuing, and are laid in masses, each containing about öOO eggs closely packed with yellowish hair from the body of the female, oval in shape and about li inches long by three-fourths of an inch wide. The eggs are laid on the trunks of trees, on the sides of houses, fences, stone walls, and other places. The females seem especially attracted to recesses where the eggs are 126 YEABBOOK OF THE DEPARTMENT OF AÖRIOÜLTURE. more or less hidden. Large holes in old trees will be found filled with them, and they are often found in the crevices between stones in a stone wall, or in the hollow of an old stump or log. The larvae (fig. 2), especially after they reach some size, feed princi- pally at night and try to hide themselves during the day. In daytime they will descend upon the larger limbs and trunk and try to find some place under the bark or in a large hole where they can secrete them- selves. It is this habit that has led to the use of burlap bands around the trunks of trees, under which they will hide during the day and where they can be found easily and destroyed. LIFE HISTORY AND DESCRIPTION OF THE BROWN-TAIL MOTH. The caterpillar of the brown-tail moth is primarily an enemy of pear, apple, cherry, peach, and other fruit trees, but it is also found commonly upon various shrubs that grow in door- yards; in Massachusetts it has begun to attack the for- est trees and now affects especially the oaks. Young oaks—oak scrub—are appar- ently particularly attractive to it at present. The insect does not hiber- nate in the egg stage, as does the gypsy moth, but as the young caterpillar. It has, like the gypsy moth, but one generation each year. FIG. Z.—The hrown-t&n moth {EuprocHs chrysmrhœa): Fe- The CggS are laid in maSSCS male moth above, male moth below, right. Slightly enlarged (original). ^^'^^^'^' ^' on the under side of the leaves in the latter part of July. The egg masses are brown and covered with hair, and each con- tains about 300 eggs. The masses.are much smaller than those of the gypsy moth, averaging about two-thirds of an inch in length by about one-fourth of an inch in width. The eggs hatch during August, and the young caterpillars feed in clusters on the upper surface of the leaves, a little later beginning to spin their winter webs by drawing together a number of leaves with silk, in which web a large number of caterpillars stow themselves away for the winter. These webs or nests, composed of leaves and silk, will average from 5 to 6 inches in length, and each will contain 200 or more caterpillars. They feed until cold weather, when all enter the web and close the exit holes. They are then about one-fourth grown. Early the following spring, as soon as the buds begin to appear on the fruit trees, they issue from the o ver-wintering THE GYPSY AND BBOWN-TAIL MOTHS. 127 nests and.attack first the buds and the blossoms, and later the foliage. The full-grown larva is about 2 inches long, reddish brown in color, with a broken white stripe on each side and two red dots on the back near the hind end. They will migrate from one tree to another, com- pletely stripping the foliage as they go. When full grown they spin their cocoons either on the tree trunks or within the leaves on the branches of the trees. 'r ^ M^ 1 PIG. 4.—Hairs of the caterpillar of the brown-tail moth, highly magni- fied (adapted from Kirkland). The moths are pure white, except that the female has a conspicuous bunch of brown hair at the tip of the abdomen, from which it derives the name '^ brown-tail moth.'^ The female expands about 1^ inches and the male is smaller. Both male and female (fig. 8) fly readily, largely at night, and are greatly attracted by electric lights. It is not alone by its damage to the foliage of fruit and other trees that the brown-tail moth is a pest. The hairs of the larvae are finely 128 YE AEBOOK OF THE DEPARTMENT OF AGRICTJLTUBE, barbed and brittle (see fig. 4), and where the caterpillar comes in con- tact with the human skin the hairs enter the skin pores, break off, and cause a severe irritation.
Recommended publications
  • Roosevelt Wild Life Bulletins the Roosevelt Wild Life Station
    SUNY College of Environmental Science and Forestry Digital Commons @ ESF Roosevelt Wild Life Bulletins The Roosevelt Wild Life Station 1926 Roosevelt Wild Life Bulletin Charles C. Adams SUNY College of Environmental Science and Forestry Follow this and additional works at: https://digitalcommons.esf.edu/rwlsbulletin Part of the Animal Sciences Commons, Biodiversity Commons, Ecology and Evolutionary Biology Commons, and the Natural Resources and Conservation Commons Recommended Citation Adams, Charles C., "Roosevelt Wild Life Bulletin" (1926). Roosevelt Wild Life Bulletins. 23. https://digitalcommons.esf.edu/rwlsbulletin/23 This Book is brought to you for free and open access by the The Roosevelt Wild Life Station at Digital Commons @ ESF. It has been accepted for inclusion in Roosevelt Wild Life Bulletins by an authorized administrator of Digital Commons @ ESF. For more information, please contact [email protected], [email protected]. VOLUME 4 OCTOBER, 1926 NUMBER 1 Roosevelt Wild Life Bulletin OF THE Roosevelt Wild Life Forest Experiment Station OF The New York State College of Forestry AT Syracuse University RELATION OF BIRDS TO WOODLOTS CONTENTS OF ROOSEVELT WILD LIFE BULLETIN (To obtain these publications see announcement on back of title page.) Roosevelt Wild Life Bulletin, Vol. i, No. i. December, 192 1. 1. Foreword Dr. George Bird Grinnell. 2. Roosevelt Wild Life State Memorial Dr. Charles C. Adams. 3. Appropriateness and Appreciation of the Roosevelt Wild Life Memorial Dr. Charles C. Adams. 4. Suggestions for Research on North American Big Game and Fur- Bearing Animals Dr. Charles C. Adams. 5. Theodore Roosevelt Sir Harry H. Johnston. 6. Roosevelt's Part in Forestry Dr.
    [Show full text]
  • Eastern Tent Caterpillar, Forest Tent Caterpillar and Fall Webworm
    Eastern Tent Caterpillar, Forest Tent Caterpillar and Fall Webworm EASTERN TENT CATERPILLAR Eastern tent caterpillar, Malacosoma americanum, feeds on cherry, apple, and plum. Full-grown caterpillars are about 1.6 inches long. Coloration varies, but in general they have black heads, and bodies marked with a mid-dorsal white stripe down the length of the back. Blue dots separate successive pairs of yellow lateral stripes. The adult moths are light brown with two diagonal white stripes across the forewings. The caterpillars' silken tents are usually found in tree forks. The larvae lay trails of silk from the communal tent to wherever they are feeding. Long trails of larvae can be seen migrating along the silken path between the tent and leaves. Eggs are laid in masses on twigs. Egg masses can be pruned from twigs during the dormant season and destroyed. Caterpillars can be handpicked from the communal tents. Bacillus thuringiensis (Bt) should be used on flowering trees to control young caterpillars. Bt is not harmful to pollinating bees. FOREST TENT CATERPILLAR The forest tent caterpillar, Malacosoma disstria, feeds on water tupelo, sweetgum, blackgum, birch, elm, maple, oak and flowering fruit trees. Full-grown caterpillars are about 1.6 inches long with light blue heads and blackish bodies with white hairs. Each segment is marked dorsally with a white keyhole-shaped spot. The adult moths are buff colored, with two darker bands on the forewings. Caterpillars are present in early spring, and upon maturity construct cocoons from folded leaves. The adults emerge in late summer and lay eggs in brown masses that encircle twigs.
    [Show full text]
  • The Gypsy Moth and Its Natural Enemies Agriculture Information Bulletin No
    THE GYPSY MOTH AND ITS NATURAL ENEMIES AGRICULTURE INFORMATION BULLETIN NO. 381 U.S. DEPARTMENT OF AGRICULTURE FOREST SERVICE i^Q^^áh nú'3^1 '/■*X. -//' ■*iS3l^ THE AUTHOR ROBERT W. CAMPBELL is principal ecologist at the North- eastern Forest Experiment Station's research unit maintained at Syracuse, N. Y., in cooperation with the State University of New York College of Environmental Science and Forestry at Syracuse University. He received his bachelor's degree in forestry from the State University of New York College of Forestry in 1953 and his master's and Ph.D. degrees in forestry from the University of Michigan in 1959 and 1961. He joined the USDA Forest Service's Northeastern Forest Experiment Station in 1961. ACKNOWLEDGMENTS My thanks to both Wayne Trimm and Robert W. Brown, whose beautiful illustrations reflect careful study of their sub- jects. I also thank the many gypsy moth watchers who have shared their observations and experiences with me. Issued February 1975 11 THE GYPSY MOTH AND ITS NATURAL ENEMIES by Robert W. Campbell CONTENTS BEHAVIOR 2 Hatch and dispersal 2 Young larvae 2 Older larvae 4 Pre-pupae and pupae 4 Adults 6 Eggs 6 MORTALITY 8 Young larvae 8 Older larvae 11 Pre-pupae 18 Pupae 18 Adults 21 Eggs 21 AGENTS THAT KILL THE SEXES DIFFERENTIALLY 22 CHANGES IN GYPSY MOTH POPULATION DENSITY 23 A FEW LAST WORDS 27 111 CAMPBELL, ROBERT W. 1974. The Gypsy Moth and its Natural Enemies. Agr. Inf. Bull. No. 381,27 p., illus. Patterns of gypsy moth behavior are described, especially those related to population density.
    [Show full text]
  • Insects That Feed on Trees and Shrubs
    INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture,
    [Show full text]
  • Economic Ornithology in Recent Entomological Publications
    Vol. 1918XXXVJ J RecentLiterature. 251 that the birds from the coastregion north of San FranciscoBay are differ- ent from either of the above. Thesehe separatesas A. californicaooclep- fica (p. 413), type locality Nicasio. He alsodiffers from Dr. Oberholser'srecent conclusionthat A. hypoleuca is merelya race of A. californica,as maintained in the A. O. U. ' Check-List,' and would giveit full specificrank. The factsin regardto this groupwould seemto be now before us and any differenceof treatment must be due to personalopinion.-- W. S. Wetmore on Pal•sochenoides mioceanus Shufeldt. •-- This name wasbased upon the fossilizeddistal end of the right femur of a bird which Dr. Shufeldt consideredas related to the Anseres. Quoting from Dr. Shufcldt'spaper we find "that this femar neverbelonged to any bird at all relatedto Sula, or to any of the Herons,or to Pelecanus,all of which havefemora possessed of somecharacters, which, though not of wide dif- ference,are quite sufficientto constitutediscriminating ones, and to point to the fact that this great extinctfowl did not belongin any of those groups,as we know them, osteologically." Now comes Mr. Wetmore with the results of another careful examination of this samebone fragment and we readthat of five charactersof the fernre' "Pal•eochenoidesagrees with the Steganopodesin four, while in only one doesit approachthe Anseres.... and it is referredwithout question to the Steganopodes."He fm•her suggeststhat it was a Pehcan-likebird of a somexvhatgeneralized type showingresemblances to the Gannetsand remotely to the Cormorants and Darters. It would seem desirable that those who name fossil birds should not fashiontheir genericnames on thoseof existingbirds as it is embarrassing to find them shifted into other families or orders where the name becomes somewhat of a misnomer! Mr.
    [Show full text]
  • Fall Webworm in Arizona Christopher Jones
    COLLEGE OF AGRICULTURE AND LIFE SCIENCES COOPERATIVE EXTENSION AZ1627 May 2014 FALL WEBWORM IN ARIZONA Christopher Jones Fall webworms are caterpillars that commonly defoliate many broadleaf deciduous trees, such as cottonwood (Populus spp.), walnut (Juglans spp.), alder (Alnus spp.), chokecherry (Prunus spp.) and elderberry (Sambucus spp.). They also attack fruit, nut and ornamental shade trees and shrubs, including pecan (Carya spp.) and mulberry (Morus spp). Fall webworms are native to North America and are present throughout the country. Fall webworms are the species Hyphantria cunea (Family Arctiidae), of which the red-headed race is most common in Arizona. Activity in the state has appeared to increase in recent years, both in geography and host species. This insect’s most obvious sign is the caterpillars’ communal silken web that can be seen at the ends of the Figure 1. Adult moths of the fall webworm vary in coloration from white to branches during late summer and fall. Female adults lay spotted. Photo credit: John Pickering, discoverlife.org. eggs on leaves during the summer months, so defoliation by the caterpillars is most conspicuous in fall. Damage does not usually cause serious stress to trees. Treatment is not typically prescribed, especially in natural settings. High population effects The effects of fall webworms are most pronounced in autumn months, when populations of second generation moths have generated multiple webs on many trees in forested areas, so much so that entire trees and shrubs will appear to have been defoliated. While the webs and defoliation may cause a loss of visual quality for some people, entomologists recognize that damage to host’s health is typically minor as defoliation occurs in the late summer and fall.
    [Show full text]
  • Faa 119 Biodiversity Analysis
    , MOLDOVA FAA 119 BIODIVERSITY ANALYSIS February 2007 This publication was produced for review by the United States Agency for International Development. It was prepared1 by DevTech Systems, Inc. under an EPIQ II subcontract to PA Government Services, Inc. This page left intentionally blank MOLDOVA FAA 119 BIODIVERSITY ANALYSIS February 2007 Prepared by DevTech Systems, Inc. under an EPIQ II subcontract to PA Government Services, Inc. Contract # EPP-I-00-03-00015-00, subcontract # EPP3R015-4S-003, Task Order 3. DISCLAIMER The author’s views expressed in this publication do not necessarily reflect the views of the United States Agency for International Development or the United States Government Cover photo credits: Jeff Ploetz, Steve Nelson, Aureliu Overcenco This page left intentionally blank TABLE OF CONTENTS ACRONYMS AND ABBREVIATIONS ...............................................................................III PREFACE ........................................................................................................................V EXECUTIVE SUMMARY..................................................................................................... VI SECTION I: INTRODUCTION AND BACKGROUND ......................................................1 SECTION II: THREATS TO BIODIVERSITY .....................................................................3 A. The Importance of Biodiversity...........................................................................................................................................
    [Show full text]
  • Browntail Moth Brochure
    Damage: Life Cycle: Browntail moth (Euproctis The caterpillars feed on the leaves of many hardwood Chrysorrhea) Browntail trees and shrubs. Common host trees and shrubs in- One generation a year. clude: Moth Four life stages; egg, larval, pupal, and adult. • Oak, apple, crabapple, cherry, hawthorn, shad- bush, serviceberry, and rugosa rose. Larval stage (caterpillars) lasts from August through to the following June. Feeding by browntail caterpillars can cause reduced In the spring, as soon as the earliest leaf buds open, growth and branch dieback. A number of years at high the caterpillars become active and leave their over- population levels can lead to mortality of trees and wintering webs to feed on tender new leaves. They shrubs. may devour the leaves as fast as the leaves develop. Identification: When young, the caterpillars return to the webs at Browntail Caterpillar: night, but later remain out on the leaves overnight, http://www.maine.gov/dacf/mfs/ • Dark brown with a broken white stripe on each side and are fully grown by late June. and two conspicuous red spots on the back. They The caterpillars then form filmy cocoons between grow to 1.5 inches (3.8 cm) in length. leaves on trees, under eaves, picnic tables, decks, etc. Why are they a problem? The browntail caterpillar has tiny (0.15 mm) hairs that Look-a-likes: Adult moths emerge from cocoons in late July and on sensitive individuals cause a skin rash similar to • Eastern tent caterpillars have a solid whitish August, laying clusters of eggs on the underside of poison ivy and/or trouble breathing.
    [Show full text]
  • ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
    NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000).
    [Show full text]
  • John Lowell Capinera
    JOHN LOWELL CAPINERA EDUCATION: Ph.D. (entomology) University of Massachusetts, 1976 M.S. (entomology) University of Massachusetts, 1974 B.A. (biology) Southern Connecticut State University, 1970 EXPERIENCE: 2015- present, Emeritus Professor, Department of Entomology and Nematology, University of Florida. 1987-2015, Professor and Chairman, Department of Entomology and Nematology, University of Florida. 1985-1987, Professor and Head, Department of Entomology, Colorado State University. 1981-1985, Associate Professor, Department of Zoology and Entomology, Colorado State University. 1976-1981, Assistant Professor, Department of Zoology and Entomology, Colorado State University. RESEARCH INTERESTS Grasshopper biology, ecology, distribution, identification and management Vegetable insects: ecology and management Terrestrial molluscs (slugs and snails): identification, ecology, and management RECOGNITIONS Florida Entomological Society Distinguished Achievement Award in Extension (1998). Florida Entomological Society Entomologist of the Year Award (1998). Gamma Sigma Delta (The Honor Society of Agriculture) Distinguished Leadership Award of Merit (1999). Elected Fellow of the Entomological Society of America (1999). Elected president of the Florida Entomological Society (2001-2002; served as vice president and secretary in previous years). “Handbook of Vegetable Pests,” authored by J.L. Capinera, named an ”Outstanding Academic Title for 2001” by Choice Magazine, a reviewer of publications for university and research libraries. “Award of Recognition” by the Entomological Society of America Formal Vegetable Insect Conference for publication of Handbook of Vegetable Pests (2002) “Encyclopedia of Entomology” was awarded Best Reference by the New York Public Library (2004), and an Outstanding Academic Title by CHOICE (2003). “Field Guide to Grasshoppers, Katydids, and Crickets of the United States” co-authored by J.L. Capinera received “Starred Review” book review in 2005 from Library Journal, a reviewer of library materials.
    [Show full text]
  • Hyphantria Cunea)
    University of Denver Digital Commons @ DU Electronic Theses and Dissertations Graduate Studies 6-1-2013 Host Use and Geographic Variation in Fall Webworms (Hyphantria cunea) Katrina J. Loewy University of Denver Follow this and additional works at: https://digitalcommons.du.edu/etd Part of the Ecology and Evolutionary Biology Commons Recommended Citation Loewy, Katrina J., "Host Use and Geographic Variation in Fall Webworms (Hyphantria cunea)" (2013). Electronic Theses and Dissertations. 379. https://digitalcommons.du.edu/etd/379 This Thesis is brought to you for free and open access by the Graduate Studies at Digital Commons @ DU. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of Digital Commons @ DU. For more information, please contact [email protected],[email protected]. HOST USE AND GEOGRAPHIC VARIATION IN FALL WEBWORMS (HYPHANTRIA CUNEA) __________ A Thesis Presented to the Faculty of Natural Sciences and Mathematics University of Denver __________ In Partial Fulfillment of the Requirements for the Degree Master of Science __________ by Katrina J. Loewy June 2013 Advisor: Shannon M. Murphy ©Copyright by Katrina J. Loewy 2013 All Rights Reserved Author: Katrina J. Loewy Title: HOST USE AND GEOGRAPHIC VARIATION IN FALL WEBWORMS (HYPHANTRIA CUNEA) Advisor: Shannon M. Murphy Degree Date: June 2013 Abstract Host use in herbivores is determined by a variety of ecological drivers, including bottom-up and top-down selective pressures such as host abundance, host plant quality, and parasitism pressure. If the relative importance and strength of interactions among these selective conditions change over an herbivore’s geographic range, local patterns of host use should change in response, evident in differing diet breadths.
    [Show full text]
  • Diptera: Oestroidea) Magdi S
    El-Hawagry Egyptian Journal of Biological Pest Control (2018) 28:46 Egyptian Journal of https://doi.org/10.1186/s41938-018-0042-3 Biological Pest Control RESEARCH Open Access Catalogue of the Tachinidae of Egypt (Diptera: Oestroidea) Magdi S. El-Hawagry Abstract Tachinid flies are an important group of parasitoids in their larval stage, and all their hosts are of the Arthropoda, almost exclusively other insects, including important insect pests in agriculture and forestry. All known Egyptian taxa of the family Tachinidae are systematically catalogued. Synonymies, type localities, type depositories, world distributions by biogeographic realm(s) and country, Egyptian localities, and dates of collection are provided. A total of 72 tachinid species belonging to 42 genera, 15 tribes, and 4 subfamilies has been treated. Keywords: Tachinid flies, Egyptian taxa, World distribution, Egyptian localities, Dates of collection Background agriculture and forestry. They typically parasitize phytopha- Tachinidae are a large and cosmopolitan family of flies gous larvae of Lepidoptera and Coleoptera or nymphs of within the superfamily Oestroidea. It is the second largest Hemiptera and Orthoptera. Consequently, tachinid flies family in the order Diptera (Irwin et al. 2003), with some have been successfully applied in programs of biological 1500 recognized genera (O’Hara 2016) and more than control against different insect pests (Stireman et al. 2006; 8500 described species (O’Hara 2013) worldwide. How- O’Hara 2008 and Cerretti and Tschorsnig 2010). ever, the estimated true diversity of the family is probably No comprehensive taxonomic studies on the family double the number of the currently known species, mak- Tachinidae have been carried out in Egypt before.
    [Show full text]