Common Butterflies and Moths (Order Lepidoptera) in the Wichita Mountains and Surrounding Areas
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												Note on Crumb's "Liberae Et Confluentae" Couplet (Noctuidae)1.2
VOLUME 39, NUMBER 1 57 FIG. 2. Pupae of Occidryas anicia bernadetta. School of Life Sciences, University of Nebraska, Lincoln, NE 68588 (S. occidentalis); V. K. Gupta, Center for Parasitic Hymenoptera, Gainesville, FL 32602 (Benjaminia sp., Pterocormus sp.); S. R. Shaw and P. M. Marsh, Systematic Entomology Laboratory, USDA-ARS, Insect Identification and Beneficial Insect Introduction Institute, Beltsville, MD 20705 (c. koebelei). STEPHEN M. SPOMER, Department of Entomology, University of Nebraska, Lincoln, Nebraska 68583 AND JAMES M. REISER, 1511 David Drive, Lincoln, Nebraska 68504. Journal of the Lepidopterists' Society 39(1), 1985, 57-59 NOTE ON CRUMB'S "LIBERAE ET CONFLUENTAE" COUPLET (NOCTUIDAE)1.2 The first major systematic treatment of the larvae of North American Noctuidae was written by Crumb (1956, Larvae of the Phalaenidae, USDA Tech. Bull. 1135. 356 pp.). It is a monumental work, containing extensive diagnostic keys, larval descriptions, geo- 1 Partially funded by the Illinois Agricultural Experiment Station Project 12-361 Biosystematics of Insects . .2 Michigan Agricultural Experiment Station Journal Article No. 11102. 58 JOURNAL OF THE LEPIDOPTERISTS' SOCIETY FIGS. 1-4. Tenth abdominal segments showing ventral and subanal regions of last instar noctuid larvae. 1 & 2, truncate or convex condition of posterior margin of venter (subanal region) (see arrows) (Alypia octomaculata); 3 & 4, medially impressed or grooved condition of the same region (see arrows) (Papaipema nebris). (Figs. 1 & 3 were photo graphed through a Leitz Aristophot, printed sizes = 9 x and 13 x, respectively; 2 & 4 were taken with the aid of a scanning electron microscope, printed sizes = 36 x; all photographs by G.L.G.) graphic distributions, and a wealth of host plant information. - 
												
												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. - 
												
												Manitoba Oakworm Moth
Manitoba Oakworm Moth because of their limited dispersal ability, and its larval preference for younger Bur Oak. This species may actually be Threatened, but data are currently insufficient to assess whether it meets thresholds for status criteria. Wildlife Species Description and e n n e Significance H n o D © : o Manitoba Oakworm Moth (Anisota manitobensis) t o h P is a medium-sized moth (forewing length 19-30 mm) in the family Saturniidae (silk worm moths). Scientific name There are four life stages and the species grows Anisota manitobensis through complete metamorphosis. Adults are brownish-orange, and females are typically Taxon pinker than darker males. The flattened, ovate Arthropods eggs are smooth and yellow, turning to brownish COSEWIC status with age. Larvae are typically dark brown to black Special Concern with paler stripes (tending to pink in later instars) with spines and thoracic horns. Pupae are brown Canadian range and approximately 3 cm long. Manitoba Reason for designation Distribution This large moth has a small global distribution, The known global and Canadian range of most of which is in Canada, and restricted to a Manitoba Oakworm Moth is restricted to southern small area in southern Manitoba and the adjacent Manitoba and extreme northern North Dakota United States. Localized population irruptions and Minnesota. The majority of the global range occurred irregularly through the 1900s, but their is in Manitoba where it has been recorded from frequency declined and the last one was in 1997; approximately 25 sites as far north as Riding no individuals have been detected since 2000. Mountain National Park. - 
												
												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, - 
												
												Phylogenetic Relationships and Historical Biogeography of Tribes and Genera in the Subfamily Nymphalinae (Lepidoptera: Nymphalidae)
Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society 0024-4066The Linnean Society of London, 2005? 2005 862 227251 Original Article PHYLOGENY OF NYMPHALINAE N. WAHLBERG ET AL Biological Journal of the Linnean Society, 2005, 86, 227–251. With 5 figures . Phylogenetic relationships and historical biogeography of tribes and genera in the subfamily Nymphalinae (Lepidoptera: Nymphalidae) NIKLAS WAHLBERG1*, ANDREW V. Z. BROWER2 and SÖREN NYLIN1 1Department of Zoology, Stockholm University, S-106 91 Stockholm, Sweden 2Department of Zoology, Oregon State University, Corvallis, Oregon 97331–2907, USA Received 10 January 2004; accepted for publication 12 November 2004 We infer for the first time the phylogenetic relationships of genera and tribes in the ecologically and evolutionarily well-studied subfamily Nymphalinae using DNA sequence data from three genes: 1450 bp of cytochrome oxidase subunit I (COI) (in the mitochondrial genome), 1077 bp of elongation factor 1-alpha (EF1-a) and 400–403 bp of wing- less (both in the nuclear genome). We explore the influence of each gene region on the support given to each node of the most parsimonious tree derived from a combined analysis of all three genes using Partitioned Bremer Support. We also explore the influence of assuming equal weights for all characters in the combined analysis by investigating the stability of clades to different transition/transversion weighting schemes. We find many strongly supported and stable clades in the Nymphalinae. We are also able to identify ‘rogue’ - 
												
												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. - 
												
												Appendix A: Common and Scientific Names for Fish and Wildlife Species Found in Idaho
APPENDIX A: COMMON AND SCIENTIFIC NAMES FOR FISH AND WILDLIFE SPECIES FOUND IN IDAHO. How to Read the Lists. Within these lists, species are listed phylogenetically by class. In cases where phylogeny is incompletely understood, taxonomic units are arranged alphabetically. Listed below are definitions for interpreting NatureServe conservation status ranks (GRanks and SRanks). These ranks reflect an assessment of the condition of the species rangewide (GRank) and statewide (SRank). Rangewide ranks are assigned by NatureServe and statewide ranks are assigned by the Idaho Conservation Data Center. GX or SX Presumed extinct or extirpated: not located despite intensive searches and virtually no likelihood of rediscovery. GH or SH Possibly extinct or extirpated (historical): historically occurred, but may be rediscovered. Its presence may not have been verified in the past 20–40 years. A species could become SH without such a 20–40 year delay if the only known occurrences in the state were destroyed or if it had been extensively and unsuccessfully looked for. The SH rank is reserved for species for which some effort has been made to relocate occurrences, rather than simply using this status for all elements not known from verified extant occurrences. G1 or S1 Critically imperiled: at high risk because of extreme rarity (often 5 or fewer occurrences), rapidly declining numbers, or other factors that make it particularly vulnerable to rangewide extinction or extirpation. G2 or S2 Imperiled: at risk because of restricted range, few populations (often 20 or fewer), rapidly declining numbers, or other factors that make it vulnerable to rangewide extinction or extirpation. G3 or S3 Vulnerable: at moderate risk because of restricted range, relatively few populations (often 80 or fewer), recent and widespread declines, or other factors that make it vulnerable to rangewide extinction or extirpation. - 
												
												INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a Synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a Historical Sketch
ZOOLOGÍA-TAXONOMÍA www.unal.edu.co/icn/publicaciones/caldasia.htm Caldasia 31(2):407-440. 2009 HACIA UNA SÍNTESIS DE LOS PAPILIONOIDEA (INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a historical sketch JOSÉ LUIS SALINAS-GUTIÉRREZ El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] CLAUDIO MÉNDEZ Escuela de Biología, Universidad de San Carlos, Ciudad Universitaria, Campus Central USAC, Zona 12. Guatemala, Guatemala. [email protected] MERCEDES BARRIOS Centro de Estudios Conservacionistas (CECON), Universidad de San Carlos, Avenida La Reforma 0-53, Zona 10, Guatemala, Guatemala. [email protected] CARMEN POZO El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] JORGE LLORENTE-BOUSQUETS Museo de Zoología, Facultad de Ciencias, UNAM. Apartado Postal 70-399, México D.F. 04510; México. [email protected]. Autor responsable. RESUMEN La riqueza biológica de Mesoamérica es enorme. Dentro de esta gran área geográfi ca se encuentran algunos de los ecosistemas más diversos del planeta (selvas tropicales), así como varios de los principales centros de endemismo en el mundo (bosques nublados). Países como Guatemala, en esta gran área biogeográfi ca, tiene grandes zonas de bosque húmedo tropical y bosque mesófi lo, por esta razón es muy importante para analizar la diversidad en la región. Lamentablemente, la fauna de mariposas de Guatemala es poco conocida y por lo tanto, es necesario llevar a cabo un estudio y análisis de la composición y la diversidad de las mariposas (Lepidoptera: Papilionoidea) en Guatemala. - 
												
												The Butterflies of Mississippi Supplement No
Journal of the Lepidopterists' Society 39(2), 1985, 134-138 THE BUTTERFLIES OF MISSISSIPPI SUPPLEMENT NO. 31 BRYANT MATHER2 AND KATHARINE MATHER 213 Mt. Salus Road, Clinton, Mississippi 39056 ABSTRACT. An annotated list of Mississippi butterflies is presented. This updated version is the fifth such list published. Six names additional to the previous lists have been included. Of the five published lists of Mississippi butterflies, this is the first to use the names and arrangement of Miller and Brown (1981) as amend ed by them in Hodges (Editor) (1983). It includes six names not in cluded in the fourth list (Mather & Mather, 1976). The growth rate has dropped to fewer than one per year as indicated in Table 1 below: TABLE 1. Published lists of Mississippi butterflies, showing rate of increase in the addition of names previously unrecorded from the state. Time Names added List Reference Names interval Names added per year 1 Weed (1894) 53 2 Hutchins (1933) 73 39 20 0.5 3 M. & M. (1958) 122 25 49 1.9 4 M. & M. (1976) 144 18 22 1.2 5 M. & M. (1984) 150 8 6 0.75 In 1958 we expressed the opinion that the list would grow to include about 160 names. We also said, "there may be cases in which the Mississippi representatives of a given species represent more than one population; if so, we do not believe that we as yet have adequate data to support such a conclusion." Now we do. Our reasons for adding the six names are summarized below. 1. - 
												
												American Lady, American Painted Lady, Vanessa Virginiensis (Drury) (Insecta: Lepidoptera: Nymphalidae: Nymphalinae)1 Donald W
EENY 449 American Lady, American Painted Lady, Vanessa virginiensis (Drury) (Insecta: Lepidoptera: Nymphalidae: Nymphalinae)1 Donald W. Hall2 The Featured Creatures collection provides in-depth profiles of insects, nematodes, arachnids, and other organisms relevant to Florida. These profiles are intended for the use of interested laypersons with some knowledge of biology as well as academic audiences. Introduction Vanessa virginiensis (Drury) has been known by a number of common names (Cech and Tudor 2005, Miller 1992) including American lady, American painted lady, painted beauty, and Hunter’s butterfly. It will be referred to here as the American lady in accord with the Checklist of North American Butterflies Occurring North of Mexico (NABA 2004). Although the adult American lady is an attractive butterfly, it is probably best known among naturalists for the characteristic nests made by its caterpillars. Figure 1. Adult American lady, Vanessa virginiensis (Drury), with dorsal view of wings. Credits: Don Hall, UF/IFAS Distribution The American lady occurs from southern Canada through- out the United States and southward to northern South America and is seen occasionally in Europe, Hawaii, and the larger Caribbean islands (Scott 1986; Opler and Krizek 1984; Cech and Tudor 2005). 1. This document is EENY 449, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date June 2009. Revised February 2018 and February 2021. Visit the EDIS website at https://edis.ifas.ufl.edu for the currently supported version of this publication. This document is also available on the Featured Creatures website at http://entomology.ifas.ufl.edu/creatures. - 
												
												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. - 
												
												Biology of Anaea Ryphea (Nymphalidae) in Campinas, Brazil
Journal of the Lepidopterists' Society 48(3), 1994, 248-257 BIOLOGY OF ANAEA RYPHEA (NYMPHALIDAE) IN CAMPINAS, BRAZIL ASTRID CALDAS Dcpartamento de Biologia Animal e Vegetal-IB, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20550-013, Brazil ABSTRACT. Anaea ryphea uses Croton fioribundus (Euphorbiacae) as its main larval food plant at Campinas, Brazil. Weekly censuses of the immature stages of A. ryphea were conducted from September 1988 to August 1989. Adults and larvae were found only from December through May. Females usually laid one egg per leaf and exhibited no plant height preference. Within individuals plants, most eggs were laid on the inter mediate leaves; they were rare on the lowest and absent on the apical, new leaves. The complete life cycle in the fi eld lasts 50 to 60 days. The pattern of devclopment in A. ryphea is similar to that described for 5 other species of Anaea. The early stages resemble closely those described for A. eurypyle, which also uses a species of Croton as its larval food plant in El Salvador. Additional key words: Hypna clytemnestra, life cycle, Memphis, Croton, Euphor biaceae. The genus Anaea Hubner includes most of the Neotropical Char axinae, although use of the generic name varies considerably among authors. Comstock (1961) assigned to Anaea the species now considered members of the Anaea troglodyta group. He used Memphis Hubner, formerly described as a generic name, as a subgenus for most of the other species of Anaea, including the blue species and A. ryphea (Cra mer). Rydon (1971) subdivided the group further, describing Foun tainea, into which he transferred ryphea.