Bioblitz! OK 2019 - Cherokee County Moth List
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Self-Repair and Self-Cleaning of the Lepidopteran Proboscis
Clemson University TigerPrints All Dissertations Dissertations 8-2019 Self-Repair and Self-Cleaning of the Lepidopteran Proboscis Suellen Floyd Pometto Clemson University, [email protected] Follow this and additional works at: https://tigerprints.clemson.edu/all_dissertations Recommended Citation Pometto, Suellen Floyd, "Self-Repair and Self-Cleaning of the Lepidopteran Proboscis" (2019). All Dissertations. 2452. https://tigerprints.clemson.edu/all_dissertations/2452 This Dissertation is brought to you for free and open access by the Dissertations at TigerPrints. It has been accepted for inclusion in All Dissertations by an authorized administrator of TigerPrints. For more information, please contact [email protected]. SELF-REPAIR AND SELF-CLEANING OF THE LEPIDOPTERAN PROBOSCIS A Dissertation Presented to the Graduate School of Clemson University In Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy ENTOMOLOGY by Suellen Floyd Pometto August 2019 Accepted by: Dr. Peter H. Adler, Major Advisor and Committee Co-Chair Dr. Eric Benson, Committee Co-Chair Dr. Richard Blob Dr. Patrick Gerard i ABSTRACT The proboscis of butterflies and moths is a key innovation contributing to the high diversity of the order Lepidoptera. In addition to taking nectar from angiosperm sources, many species take up fluids from overripe or sound fruit, plant sap, animal dung, and moist soil. The proboscis is assembled after eclosion of the adult from the pupa by linking together two elongate galeae to form one tube with a single food canal. How do lepidopterans maintain the integrity and function of the proboscis while foraging from various substrates? The research questions included whether lepidopteran species are capable of total self- repair, how widespread the capability of self-repair is within the order, and whether the repaired proboscis is functional. -
The Adaptive Function of Tiger Moth Clicks Against Echolocating Bats: an Experimental and Synthetic Approach
2811 The Journal of Experimental Biology 209, 2811 Published by The Company of Biologists 2006 doi:10.1242/jeb.02367 Corrigendum Ratcliffe, J. M. and Fullard, J. H. (2005). The adaptive function of tiger moth clicks against echolocating bats: an experimental and synthetic approach. J. Exp. Biol. 208, 4689-4698 There was in error in the legend to Fig.·3. The published version reads: Parameter functions for three gleaning echolocation call sequences of an individual M. septentrionalis. (A) Attack on non-arctiid moth; (B) attack on muted C. tenera; (C) attack on intact C. tenera. See Fig.·1 for further details. The correct version should read: Fig.·3. Parameter functions for three aerial hawking echolocation call sequences of an individual M. septentrionalis. (A) Attack on non-arctiid moth; (B) attack on muted C. tenera; (C) attack on intact C. tenera. See Fig.·1 for further details. The authors apologise for this mistake and any inconvenience caused to readers. THE JOURNAL OF EXPERIMENTAL BIOLOGY The Journal of Experimental Biology 208, 4689-4698 4689 Published by The Company of Biologists 2005 doi:10.1242/jeb.01927 The adaptive function of tiger moth clicks against echolocating bats: an experimental and synthetic approach John M. Ratcliffe* and James H. Fullard Department of Zoology, University of Toronto at Mississauga, Toronto, Ontario, M5S 3G5, Canada *Author for correspondence at present address: Department of Neurobiology and Behavior, Cornell University, Seeley G. Mudd Hall, Ithaca, NY 14853, USA (e-mail: [email protected]) Accepted 12 October 2005 Summary We studied the efficiency and effects of the multiple during aerial hawking attacks: tymbal clicks were sensory cues of tiger moths on echolocating bats. -
LITERA TURE CITED CLOKEY, IW 951. Flora Of
24 JOURNAL OF THE LEPIDOPI'ERISTS' SOCIETY LITERA TURE CITED CLOKEY, I. W. 951. Flora of the Charleston Mountains, Clark County, Nevada. Univ. Calif. Publ. Botany, No. 24. EMMEL, J. F. & O. SHIELDS. The biology of Plebejus (Icaricia) shasta in the western United Sta s (Lycaenidae). J. Res. Lepid., in press. FERRIS, C. D. 976. Revisionary notes on Plebejus (Icaricia) shasta (Edwards). Bull. Allyn Mus m, No. 36. GARTH,]. S. 1 8. Report of the Lorquin Entomological Society of Los Angeles. Proc. So. Calif. A ad. Sci. 27: 93-94. HALL, E. R. 1946. Mammals of Nevada. Univ. Calif. Press, Berkeley. HOWE, W. H. 1975. The butterflies of North America. Doubleday, Garden City, N.Y. JOHNSON, N. K. 1965. The breeding avifaunas of the Sheep and Spring ranges in southern Nevada. Condor 67: 93-124. SMITHE, F. B. 1975. Naturalist's color guide. Am. Mus. Nat. Hist., New York. Journal of the Lepidopterists' Societ!J 34(1), 1980,24 THE IDENTITY OF THE PLANT REFERRED TO AS ANDROMEDA BY W. T. M. FORBES The name Andromeda has been used ambiguously in the lepidopteran literature. A striking example is in its mention as a larval host for Datana major Grote and Robinson and Datana ranaeceps (Guerin) by Forbes (1948, Lepidoptera of New York ... II: Cornell U. Agric. Expt. Sta. Mem. 274, p. 215). The ranges of both of these species lie almost entirely to the south and east of the only species of the genus Andromeda covered by Fernald (1950, Gray's Manual of Botany, 8th ed. Amer. Book Co., N.Y., p. -
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 -
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. -
GIS Handbook Appendices
Aerial Survey GIS Handbook Appendix D Revised 11/19/2007 Appendix D Cooperating Agency Codes The following table lists the aerial survey cooperating agencies and codes to be used in the agency1, agency2, agency3 fields of the flown/not flown coverages. The contents of this list is available in digital form (.dbf) at the following website: http://www.fs.fed.us/foresthealth/publications/id/id_guidelines.html 28 Aerial Survey GIS Handbook Appendix D Revised 11/19/2007 Code Agency Name AFC Alabama Forestry Commission ADNR Alaska Department of Natural Resources AZFH Arizona Forest Health Program, University of Arizona AZS Arizona State Land Department ARFC Arkansas Forestry Commission CDF California Department of Forestry CSFS Colorado State Forest Service CTAES Connecticut Agricultural Experiment Station DEDA Delaware Department of Agriculture FDOF Florida Division of Forestry FTA Fort Apache Indian Reservation GFC Georgia Forestry Commission HOA Hopi Indian Reservation IDL Idaho Department of Lands INDNR Indiana Department of Natural Resources IADNR Iowa Department of Natural Resources KDF Kentucky Division of Forestry LDAF Louisiana Department of Agriculture and Forestry MEFS Maine Forest Service MDDA Maryland Department of Agriculture MADCR Massachusetts Department of Conservation and Recreation MIDNR Michigan Department of Natural Resources MNDNR Minnesota Department of Natural Resources MFC Mississippi Forestry Commission MODC Missouri Department of Conservation NAO Navajo Area Indian Reservation NDCNR Nevada Department of Conservation -
Lepidoptera: Noctuidae) 1880 in Louisiana by Vernon Antoine Brou Jr., 74320 Jack Loyd Road, Abita Springs, Louisiana 70420 Email: [email protected]
Catocala carissima Hulst, (Lepidoptera: Noctuidae) 1880 in Louisiana by Vernon Antoine Brou Jr., 74320 Jack Loyd Road, Abita Springs, Louisiana 70420 email: [email protected] a b Fig. 1. Catocala carissima: a, male, b. female. 10 Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 5 number of adults 0 Fig. 2. Catocala carissima captured mostly in light traps in Louisiana. n = 294 G. D. Hulst (1880) described Catocala cara var. carissima as a variation of Catocala cara Guenee, 1852. Barnes and McDunnough (1918) pictured adult, larva and genitalia ofcara , and said of cara, "in the southern part of its range (Texas to Florida), it forms the race carissima Hulst". Forbes (1954) states of cara, "The southern variation carissima Hulst is larger, browner, with pale apical patch; it is Floridian, but odd specimens and transitions occur as far north as New Jersey". Chapin and Callahan (1967) reported cara carissima from the Baton Rouge area without specific locality. Sargent (1976) reported cara form "carissima" in Florida, and that it is predominately southern, but taken in Long Island, New York. Covell (1984) states of cara, " form carissima more common than typical form southward". Knudson and Bordelon (1999) listed and illustrated carissima from Texas. Heppner (2003) listed carissima from Florida and occurring in the Fig. 3. Parish records by this author. southeast U.S.: Maryland to Florida and Missouri to Texas. I have captured the large underwing moth Catocala carissima Hulst (Fig.1) in Louisiana from the end of May through the end of November (Fig. 2) and it occurs commonly across the state (Fig. -
Bionomics of Bagworms (Lepidoptera: Psychidae)
ANRV363-EN54-11 ARI 27 August 2008 20:44 V I E E W R S I E N C N A D V A Bionomics of Bagworms ∗ (Lepidoptera: Psychidae) Marc Rhainds,1 Donald R. Davis,2 and Peter W. Price3 1Department of Entomology, Purdue University, West Lafayette, Indiana, 47901; email: [email protected] 2Department of Entomology, Smithsonian Institution, Washington D.C., 20013-7012; email: [email protected] 3Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona, 86011-5640; email: [email protected] Annu. Rev. Entomol. 2009. 54:209–26 Key Words The Annual Review of Entomology is online at bottom-up effects, flightlessness, mating failure, parthenogeny, ento.annualreviews.org phylogenetic constraint hypothesis, protogyny This article’s doi: 10.1146/annurev.ento.54.110807.090448 Abstract Copyright c 2009 by Annual Reviews. The bagworm family (Lepidoptera: Psychidae) includes approximately All rights reserved 1000 species, all of which complete larval development within a self- 0066-4170/09/0107-0209$20.00 enclosing bag. The family is remarkable in that female aptery occurs in ∗The U.S. Government has the right to retain a over half of the known species and within 9 of the 10 currently recog- nonexclusive, royalty-free license in and to any nized subfamilies. In the more derived subfamilies, several life-history copyright covering this paper. traits are associated with eruptive population dynamics, e.g., neoteny of females, high fecundity, dispersal on silken threads, and high level of polyphagy. Other salient features shared by many species include a short embryonic period, developmental synchrony, sexual segrega- tion of pupation sites, short longevity of adults, male-biased sex ratio, sexual dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case. -
Conservation and Management of Eastern Big-Eared Bats a Symposium
Conservation and Management of Eastern Big-eared Bats A Symposium y Edited b Susan C. Loeb, Michael J. Lacki, and Darren A. Miller U.S. Department of Agriculture Forest Service Southern Research Station General Technical Report SRS-145 DISCLAIMER The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. Papers published in these proceedings were submitted by authors in electronic media. Some editing was done to ensure a consistent format. Authors are responsible for content and accuracy of their individual papers and the quality of illustrative materials. Cover photos: Large photo: Craig W. Stihler; small left photo: Joseph S. Johnson; small middle photo: Craig W. Stihler; small right photo: Matthew J. Clement. December 2011 Southern Research Station 200 W.T. Weaver Blvd. Asheville, NC 28804 Conservation and Management of Eastern Big-eared Bats: A Symposium Athens, Georgia March 9–10, 2010 Edited by: Susan C. Loeb U.S Department of Agriculture Forest Service Southern Research Station Michael J. Lacki University of Kentucky Darren A. Miller Weyerhaeuser NR Company Sponsored by: Forest Service Bat Conservation International National Council for Air and Stream Improvement (NCASI) Warnell School of Forestry and Natural Resources Offield Family Foundation ContEntS Preface . v Conservation and Management of Eastern Big-Eared Bats: An Introduction . 1 Susan C. Loeb, Michael J. Lacki, and Darren A. Miller Distribution and Status of Eastern Big-eared Bats (Corynorhinus Spp .) . 13 Mylea L. Bayless, Mary Kay Clark, Richard C. Stark, Barbara S. -
Lepidoptera: Psychidae)
Eur. J. Entomol. 111(1): 121–136, 2014 doi: 10.14411/eje.2014.013 ISSN 1210-5759 (print), 1802-8829 (online) Evaluation of criteria for species delimitation of bagworm moths (Lepidoptera: Psychidae) VERONICA CHEVASCO1, JELMER A. ELZINGA1, JOHANNA MAPPES2 and ALESSANDRO GRAPPUTO3 1 Department of Biological and Environmental Science, P.O. Box 35, FI-40014 University of Jyväskylä, Finland; e-mails: [email protected]; [email protected] 2 Center of Excellence in Biological Interactions, P.O. Box 35, FI-40014 University of Jyväskylä, Finland; e-mail: [email protected] 3 Department of Biology, University of Padova, Via Ugo Bassi 58/B, I-35121 Padova, Italy; e-mail: [email protected] Key words. Lepidoptera, Psychidae, Dahlica, Siederia, DNA barcoding, COI Abstract. Accurate identification of species is fundamental for biological research and necessary for species conservation. DNA bar- coding is particularly useful when identification using morphological characteristics is laborious and/or unreliable. However, bar- codes for species are dependent on the availability of reference sequences from correctly identified specimens. The traditional use of morphology to delimit the species boundaries of Finnish bagworm moths (Lepidoptera: Psychidae: Naryciinae: Dahliciini) is contro- versial because there is overlap in their morphological characteristics. In addition, there are no suitable molecular markers. We veri- fied the delimitation of seven out of eight previously described taxa, by using the currently standardized COI barcode and phylogenetic inference based on fragments of mitochondrial (COI) and nuclear genes (MDH). Moreover, we compared the results of molecular methods with the outcome of geometric morphometrics. Based on molecular identification, our findings indicate that there are five sexual species (Dahlica and Siederia spp.) and two parthenogenetic species (D. -
Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometro
Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, & Noctuoidea) Biodiversity Inventory of the University of Florida Natural Area Teaching Lab Hugo L. Kons Jr. Last Update: June 2001 Abstract A systematic check list of 489 species of Lepidoptera collected in the University of Florida Natural Area Teaching Lab is presented, including 464 species in the superfamilies Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, and Noctuoidea. Taxa recorded in Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, and Thyrididae are also included. Moth taxa were collected at ultraviolet lights, bait, introduced Bahiagrass (Paspalum notatum), and by netting specimens. A list of taxa recorded feeding on P. notatum is presented. Introduction The University of Florida Natural Area Teaching Laboratory (NATL) contains 40 acres of natural habitats maintained for scientific research, conservation, and teaching purposes. Habitat types present include hammock, upland pine, disturbed open field, cat tail marsh, and shallow pond. An active management plan has been developed for this area, including prescribed burning to restore the upland pine community and establishment of plots to study succession (http://csssrvr.entnem.ufl.edu/~walker/natl.htm). The site is a popular collecting locality for student and scientific collections. The author has done extensive collecting and field work at NATL, and two previous reports have resulted from this work, including: a biodiversity inventory of the butterflies (Lepidoptera: Hesperioidea & Papilionoidea) of NATL (Kons 1999), and an ecological study of Hermeuptychia hermes (F.) and Megisto cymela (Cram.) in NATL habitats (Kons 1998). Other workers have posted NATL check lists for Ichneumonidae, Sphecidae, Tettigoniidae, and Gryllidae (http://csssrvr.entnem.ufl.edu/~walker/insect.htm).