Giant Silkworm Moths Ric Bessin, Extension Specialist Entfact-008
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Caterpillars Moths Butterflies Woodies
NATIVE Caterpillars Moths and utter flies Band host NATIVE Hackberry Emperor oodies PHOTO : Megan McCarty W Double-toothed Prominent Honey locust Moth caterpillar Hackberry Emperor larva PHOTO : Douglas Tallamy Big Poplar Sphinx Number of species of Caterpillars n a study published in 2009, Dr. Oaks (Quercus) 557 Beeches (Fagus) 127 Honey-locusts (Gleditsia) 46 Magnolias (Magnolia) 21 Double-toothed Prominent ( Nerice IDouglas W. Tallamy, Ph.D, chair of the Cherries (Prunus) 456 Serviceberry (Amelanchier) 124 New Jersey Tea (Ceanothus) 45 Buttonbush (Cephalanthus) 19 bidentata ) larvae feed exclusively on elms Department of Entomology and Wildlife Willows (Salix) 455 Larches or Tamaracks (Larix) 121 Sycamores (Platanus) 45 Redbuds (Cercis) 19 (Ulmus), and can be found June through Ecology at the University of Delaware Birches (Betula) 411 Dogwoods (Cornus) 118 Huckleberry (Gaylussacia) 44 Green-briar (Smilax) 19 October. Their body shape mimics the specifically addressed the usefulness of Poplars (Populus) 367 Firs (Abies) 117 Hackberry (Celtis) 43 Wisterias (Wisteria) 19 toothed shape of American elm, making native woodies as host plants for our Crabapples (Malus) 308 Bayberries (Myrica) 108 Junipers (Juniperus) 42 Redbay (native) (Persea) 18 them hard to spot. The adult moth is native caterpillars (and obviously Maples (Acer) 297 Viburnums (Viburnum) 104 Elders (Sambucus) 42 Bearberry (Arctostaphylos) 17 small with a wingspan of 3-4 cm. therefore moths and butterflies). Blueberries (Vaccinium) 294 Currants (Ribes) 99 Ninebark (Physocarpus) 41 Bald cypresses (Taxodium) 16 We present here a partial list, and the Alders (Alnus) 255 Hop Hornbeam (Ostrya) 94 Lilacs (Syringa) 40 Leatherleaf (Chamaedaphne) 15 Honey locust caterpillar feeds on honey number of Lepidopteran species that rely Hickories (Carya) 235 Hemlocks (Tsuga) 92 Hollies (Ilex) 39 Poison Ivy (Toxicodendron) 15 locust, and Kentucky coffee trees. -
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. -
Butterflies and Moths of Brevard County, Florida, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Species of Greatest Conservation Need 2015 Wildlife Action Plan
RHODE ISLAND SPECIES OF GREATEST CONSERVATION NEED 2015 WILDLIFE ACTION PLAN RI SGCN 2015 (454) Contents SGCN Mammals ............................................................................................................................. 2 SGCN Birds .................................................................................................................................... 3 SGCN Herptofauna ......................................................................................................................... 6 SGCN Fish ...................................................................................................................................... 7 SGCN Invertebrates ........................................................................................................................ 9 1 RHODE ISLAND SPECIES OF GREATEST CONSERVATION NEED 2015 WILDLIFE ACTION PLAN SGCN Mammals (21) Scientific Name Common Name Balaenoptera physalus Fin Whale Eptesicus fuscus Big Brown Bat Eubalaena glacialis North Atlantic Right Whale Lasionycteris noctivagans Silver-haired Bat Lasiurus borealis Eastern Red Bat Lasiurus cinereus Hoary Bat Lynx rufus Bobcat Megaptera novaeangliae Humpback Whale Microtus pennsylvanicus provectus Block Island Meadow Vole Myotis leibii Eastern Small-footed Myotis Myotis lucifugus Little Brown Myotis Myotis septentrionalis Northern Long-eared Bat Perimyotis subflavus Tri-colored Bat Phoca vitulina Harbor Seal Phocoena phocoena Harbor Porpoise Scalopus aquaticus Eastern Mole Sorex (Otisorex) fumeus Smoky -
PORTABLE OUTDOOR CAGES for MATING FEMALE GIANT SILKWORM MOTHS (SATURNIIDAE)L
VOLUME 30, NUMBER 2 95 PORTABLE OUTDOOR CAGES FOR MATING FEMALE GIANT SILKWORM MOTHS (SATURNIIDAE)l THOMAS A. MILLER 2 AND WILLIAM J. COOPER ~ U. S. Army Medical Bioengineering Research and Development Laboratory, USAMBRDL BLDG 568, Fort Detrick, Maryland 21701 Like many lepidopterists who colonize and study the saturniids, we must find time apart from professional duties and other daily activities to pursue our interest in this family of moths. Therefore, our rearing methods must be both efficient and reliable if we are to accomplish any thing other than the mere maintenance of colonies. Although most of the saturniid species we have reared can be colonized for many genera tions without difficulty, we have at times had a particular problem obtain ing fertile eggs to perpetuate existing colonies or to begin new ones. This problem has been a function largely of limited available time to ensure the mating of females either by hand mating or by the use of indoor cages. For this reason we undertook an evaluation of methods for the routine, unattended mating of female saturniids indigenous to our area. We decided beforehand that the tying out of virgin females and the use of various-size stationary cages or traps (Collins & Weast, 1961; Quesada, 1967; Villiard, 1969) were not suitable to meet our requirements. Our approach, therefore, was to construct and test a series of portable out door cages that could be substituted locally for tying out or stationary cages and could also be easily transported for use in remote field areas. These cages were designed to minimize or prevent the escape of females placed therein while permitting pheromone-seeking males access for the purpose of copulation. -
Moths of North Carolina - Early Draft 1
Saturniidae Anisota stigma Spiny Oakworm Moth 20 n=0 • • • High Mt. • • • • N 10 • • •• u • • • • m • • • • b • • 0 • • • e • • • • r 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 • 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 NC counties: 36 • Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec o • • 20 • • f n=25 • = Sighting or Collection Low Mt. High counts of: • in NC since 2001 F • = Not seen since 2001 l 10 45 - Beaufort - 2006-08-21 • i 45 - Beaufort - 2010-08-22 g Status Rank h 40 - Stokes - 1997-07-08 0 NC US NC Global t 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 D Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec a 20 20 t n=21 n=65 e Pd CP s 10 10 0 0 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 15 5 25 Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Three periods to each month: 1-10 / 11-20 / 21-31 FAMILY: Saturniidae SUBFAMILY: Caratocaminae TRIBE: TAXONOMIC_COMMENTS: One of four species in this genus that occurs in North Carolina (3 others occur north of Mexico -- Tuskes et al. -
Hyalophora Cecropia): Morphological, Behavioral, and Biophysical Differences
University of Massachusetts Medical School eScholarship@UMMS Neurobiology Publications and Presentations Neurobiology 2017-03-22 Dimorphic cocoons of the cecropia moth (Hyalophora cecropia): Morphological, behavioral, and biophysical differences Patrick A. Guerra University of Massachusetts Medical School Et al. Let us know how access to this document benefits ou.y Follow this and additional works at: https://escholarship.umassmed.edu/neurobiology_pp Part of the Neuroscience and Neurobiology Commons Repository Citation Guerra PA, Reppert SM. (2017). Dimorphic cocoons of the cecropia moth (Hyalophora cecropia): Morphological, behavioral, and biophysical differences. Neurobiology Publications and Presentations. https://doi.org/10.1371/journal.pone.0174023. Retrieved from https://escholarship.umassmed.edu/ neurobiology_pp/207 Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 License. This material is brought to you by eScholarship@UMMS. It has been accepted for inclusion in Neurobiology Publications and Presentations by an authorized administrator of eScholarship@UMMS. For more information, please contact [email protected]. RESEARCH ARTICLE Dimorphic cocoons of the cecropia moth (Hyalophora cecropia): Morphological, behavioral, and biophysical differences Patrick A. Guerra¤*, Steven M. Reppert* Department of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America ¤ Current address: Department of Biological Sciences, University of Cincinnati, -
Clicking Caterpillars: Acoustic Aposematism in Antheraea Polyphemus and Other Bombycoidea Sarah G
993 The Journal of Experimental Biology 210, 993-1005 Published by The Company of Biologists 2007 doi:10.1242/jeb.001990 Clicking caterpillars: acoustic aposematism in Antheraea polyphemus and other Bombycoidea Sarah G. Brown1, George H. Boettner2 and Jayne E. Yack1,* 1Department of Biology, Carleton University, Ottawa, Ontario, K1S 5B6, Canada and 2Plant Soil and Insect Sciences, University of Massachusetts, Amherst, MA 01003, USA *Author for correspondence (e-mail: [email protected]) Accepted 21 November 2006 Summary Acoustic signals produced by caterpillars have been correlated sound production with attack, and an increase documented for over 100 years, but in the majority of in attack rate was positively correlated with the number of cases their significance is unknown. This study is the first signals produced. In addition, sound production typically to experimentally examine the phenomenon of audible preceded or accompanied defensive regurgitation. sound production in larval Lepidoptera, focusing on a Bioassays with invertebrates (ants) and vertebrates (mice) common silkmoth caterpillar, Antheraea polyphemus revealed that the regurgitant is deterrent to would-be (Saturniidae). Larvae produce airborne sounds, predators. Comparative evidence revealed that other resembling ‘clicks’, with their mandibles. Larvae typically Bombycoidea species, including Actias luna (Saturniidae) signal multiple times in quick succession, producing trains and Manduca sexta (Sphingidae), also produce airborne that last over 1·min and include 50–55 clicks. Individual sounds upon attack, and that these sounds precede clicks within a train are on average 24.7·ms in duration, regurgitation. The prevalence and adaptive significance of often consisting of multiple components. Clicks are audible warning sounds in caterpillars is discussed. -
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, -
Moth Tails Divert Bat Attack: Evolution of Acoustic Deflection
Moth tails divert bat attack: Evolution of acoustic deflection Jesse R. Barbera,1, Brian C. Leavella, Adam L. Keenera, Jesse W. Breinholtb, Brad A. Chadwellc, Christopher J. W. McClurea,d, Geena M. Hillb, and Akito Y. Kawaharab,1 aDepartment of Biological Sciences, Boise State University, Boise, ID 83725; bFlorida Museum of Natural History, McGuire Center for Lepidoptera and Biodiversity, University of Florida, Gainesville, FL 32611; cDepartment of Anatomy and Neurobiology, Northeast Ohio Medical University, Rootstown, OH 44272; and dPeregrine Fund, Boise, ID 83709 Edited by May R. Berenbaum, University of Illinois at Urbana-Champaign, Urbana, IL, and approved January 28, 2015 (received for review November 15, 2014) Adaptations to divert the attacks of visually guided predators the individuals that were tested. Interactions took place under have evolved repeatedly in animals. Using high-speed infrared darkness in a sound-attenuated flight room. We recorded each videography, we show that luna moths (Actias luna) generate an engagement with infrared-sensitive high-speed cameras and ul- acoustic diversion with spinning hindwing tails to deflect echolo- trasonic microphones. To constrain the moths’ flight to a ∼1m2 cating bat attacks away from their body and toward these non- area surveyed by the high-speed cameras, we tethered luna moths essential appendages. We pit luna moths against big brown bats from the ceiling with a monofilament line. (Eptesicus fuscus) and demonstrate a survival advantage of ∼47% for moths with tails versus those that had their tails removed. The Results and Discussion benefit of hindwing tails is equivalent to the advantage conferred Bats captured 34.5% (number of moths presented; n = 87) of to moths by bat-detecting ears. -
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.