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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 -
Rare Native Animals of RI
RARE NATIVE ANIMALS OF RHODE ISLAND Revised: March, 2006 ABOUT THIS LIST The list is divided by vertebrates and invertebrates and is arranged taxonomically according to the recognized authority cited before each group. Appropriate synonomy is included where names have changed since publication of the cited authority. The Natural Heritage Program's Rare Native Plants of Rhode Island includes an estimate of the number of "extant populations" for each listed plant species, a figure which has been helpful in assessing the health of each species. Because animals are mobile, some exhibiting annual long-distance migrations, it is not possible to derive a population index that can be applied to all animal groups. The status assigned to each species (see definitions below) provides some indication of its range, relative abundance, and vulnerability to decline. More specific and pertinent data is available from the Natural Heritage Program, the Rhode Island Endangered Species Program, and the Rhode Island Natural History Survey. STATUS. The status of each species is designated by letter codes as defined: (FE) Federally Endangered (7 species currently listed) (FT) Federally Threatened (2 species currently listed) (SE) State Endangered Native species in imminent danger of extirpation from Rhode Island. These taxa may meet one or more of the following criteria: 1. Formerly considered by the U.S. Fish and Wildlife Service for Federal listing as endangered or threatened. 2. Known from an estimated 1-2 total populations in the state. 3. Apparently globally rare or threatened; estimated at 100 or fewer populations range-wide. Animals listed as State Endangered are protected under the provisions of the Rhode Island State Endangered Species Act, Title 20 of the General Laws of the State of Rhode Island. -
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. -
Saturniidae) of Rio Grande Do Sul State, Brazil
214214 JOURNAL OF THE LEPIDOPTERISTS’ SOCIETY Journal of the Lepidopterists’ Society 63(4), 2009, 214-232 ARSENURINAE AND CERATOCAMPINAE (SATURNIIDAE) OF RIO GRANDE DO SUL STATE, BRAZIL ANDERSONN SILVEIRA PRESTES Laboratório de Entomologia, Pontifícia Universidade Católica do Rio Grande do Sul. Caixa postal 1429, 90619-900 Porto Alegre, RS, Brazil; email: [email protected] FABRÍCIO GUERREIRO NUNES Laboratório de Entomologia, Pontifícia Universidade Católica do Rio Grande do Sul. Caixa postal 1429, 90619-900 Porto Alegre, RS, Brazil; email: [email protected] ELIO CORSEUIL Laboratório de Entomologia, Pontifícia Universidade Católica do Rio Grande do Sul. Caixa postal 1429, 90619-900 Porto Alegre, RS, Brazil; email: [email protected] AND ALFRED MOSER Avenida Rotermund 1045, 93030-000 São Leopoldo, RS, Brazil; email: [email protected] ABSTRACT. The present work aims to offer a list of Arsenurinae and Ceratocampinae species known to occur in Rio Grande do Sul, Brazil. The list is based on bibliographical data, newly collected specimens, and previously existing museum collections. The Arsenurinae are listed in the following genera (followed by number of species): Arsenura Duncan, 1841 (4), Caio Travassos & Noronha, 1968 (1), Dysdaemonia Hübner, [1819] (1), Titaea Hübner, [1823] (1), Paradaemonia Bouvier, 1925 (2), Rhescyntis Hübner, [1819] (1), Copiopteryx Duncan, 1841 (2). Cerato- campinae are listed in Adeloneivaia Travassos, 1940 (3), Adelowalkeria Travassos, 1941 (2), Almeidella Oiticica, 1946 (2), Cicia Oiticica, 1964 (2), Citheronia Hübner, [1819] (4), Citioica Travassos & Noronha, 1965 (1), Eacles Hübner, [1819] (4), Mielkesia Lemaire, 1988 (1), Neocarne- gia Draudt, 1930 (1), Oiticella Travassos & Noronha, 1965 (1), Othorene Boisduval, 1872 (2), Procitheronia Michener, 1949 (1), Psilopygida Michener, 1949 (2), Scolesa Michener, 1949 (3) and Syssphinx Hübner, [1819] (1). -
First Record of Citheronia Regalis (Lepidoptera: Saturniidae) Feeding on Cotinus Obovatus (Anacardiaceae) Author(S): Gary R
First Record of Citheronia regalis (Lepidoptera: Saturniidae) Feeding on Cotinus obovatus (Anacardiaceae) Author(s): Gary R. Graves Source: Florida Entomologist, 100(2):474-475. Published By: Florida Entomological Society https://doi.org/10.1653/024.100.0210 URL: http://www.bioone.org/doi/full/10.1653/024.100.0210 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Scientific Notes First record of Citheronia regalis (Lepidoptera: Saturniidae) feeding on Cotinus obovatus (Anacardiaceae) Gary R. Graves1,2,* The regal moth (Citheronia regalis F.; Lepidoptera: Saturniidae) 2016) shows historic and recent records of C. regalis for only 11 of was historically distributed in eastern North America from southern the 34 counties in which natural populations of smoketree have been New England and southern Michigan, south to southern Florida, and documented (Davis & Graves 2016). west to eastern Nebraska and eastern Texas (Tuskes et al. -
Largest Species, Citheronia Splendens Sinaloensis (Hoffmann) and Ea Cles Oslari Rothschild, Is Poorly Known
Journal of the Lepidopterists' Society 40(4), 1986, 264- 270 BIOLOGY AND IMMATURE STAGES OF CITHERONIA SPLENDENS SINALOENSIS AND EACLES OSLARI IN ARIZONA (SATURNIIDAE) PAUL M. TUSKES 7900 Cambridge IllD, Houston, Texas 77054 ABSTRACT. Citheronia splendens sinaloensis and Eacles oslari occur in Cochise, Pima, and Santa Cruz counties in southern Arizona. Both species have one generation per year. The flight season of E. oslari extends from early June to mid-August, and the larval host plants include Quercus species. The flight season of C. splendens extends from July to mid-August, and the larval host plants include wild cotton, manzanita, and New Mexico evergreen sumac. The immature stages are described for the first time. The citheroniine fauna of Arizona is unique in that all seven species are primarily of Mexican origin (Tuskes 1985). The biology of the two largest species, Citheronia splendens sinaloensis (Hoffmann) and Ea cles oslari Rothschild, is poorly known. Ferguson (1971) illustrated the adults, summarized existing information, and indicated that their im mature stages were undescribed. The purpose of this paper is to de scribe the immature stages of both species and to present additional biological and distributional information. Citheronia splendens sinaloensis (Figs. 1-4) Citheronia splendens sinaloensis is the only member of the genus presently known to occur in Arizona. Citheronia mexicana G. & R. occurs just south of Arizona, in Sonora, Mexico. Although reported from Arizona before the turn of the century, there are no recent United States records. Citheronia regalis (F.) and C. sepulcralis (Druce) are common in the eastern or central United States but do not occur farther west than central Texas. -
(Larva), Regal Moth Or Royal Walnut Moth (Adult), Citheronia Regalis (Fabricius) (Insecta: Lepidoptera: Saturniidae: Ceratocampinae)1 Donald W
EENY-052 Hickory Horned Devil (Larva), Regal Moth or Royal Walnut Moth (Adult), Citheronia regalis (Fabricius) (Insecta: Lepidoptera: Saturniidae: Ceratocampinae)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 The regal or royal walnut moth, Citheronia regalis (Fabri- cius), is one of our largest and most spectacular moths. Like most other moths, it is nocturnal but is sometimes observed at lights. The imposing larva, known as the hickory horned devil, is most often observed when it is full grown and comes down from the trees to wander in search of a site for pupation. The regal moth is a beautiful and fascinating member of our native fauna, and its larvae should not be killed. If a larva is found crawling on pavement or in an area of thick turf grass where it would have difficulty burrowing, it should be moved to an area of soft soil or a mulched area where it can Figure 1. Hickory horned devil caterpillar, of the regal moth, Citheronia burrow for pupation. regalis (Fabricius), showing size in relation to an adult human’s hand. Credits: Lyle J. Buss, UF/IFAS 1. This document is EENY-052, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date August 1998. Revised September 2014 and February 2021. Visit the EDIS website at https://edis.ifas.ufl.edu for the currently supported version of this publication. -
Lepidoptera: Saturniidae, Ceratocampinae)
48 Nachr. entomol. Ver. Apollo, N. F. 23 (1/2): 49–52 (2002) 49 A new Citheronia from Bolivia and its immature stages (Lepidoptera: Saturniidae, Ceratocampinae) Kirby L. Wolfe1 and Daniel Herbin Kirby L. Wolfe, 3090 Cordrey Drive, Escondido, California 92029, U.S.A., email: [email protected] Daniel Herbin, 28 chemin du Moulin, F-31320 Pechabou, France; email: [email protected] Abstract: Citheronia maureillei n. sp. is described from der Zucht fraßen die Raupen an Malosma (= Rhus) laurina south-central Bolivia. It is related to the Citheronia brissotii und Schinus molle (Anacardiaceae), Liquidambar (Hamame- group and is mainly recognizable by the mostly yellow tho- lidaceae) sowie Salix caprea (Salicaceae). rax, rounded wings and few internervular spots in most spe- cimens. This species closely resembles Citheronia guayaquila Introduction in appearance and Citheronia johnsoni in genitalia. Male and female genitalia are figured and immature stages The genus Citheronia encompasses about 20 species are described and illustrated in color. Larvae fed in of mostly large yellow, gray and reddish moths with the laboratory on Malosma laurina and Schinus molle relatively narrow triangular wings and robust torpedo- (Anacardiaceae), Liquidambar (Hamamelidaceae) and Salix caprea (Salicaceae). shaped bodies striped yellow and red. Within this genus there is sometimes more intraspecific regional variation Key words: Bolivia, Ceratocampinae, Citheronia, immature than variation between species, and examination of the stages, larvae, Malosma, maureillei, Neotropical, Saturniidae. genitalia, fortunately usually decisively distinct, often Un nouveau Citheronia de Bolivie et ses stades larvaires becomes a necessity for specific identification. In the (Lepidoptera: Saturniidae, Ceratocampinae) present species, external morphological characters were immediately obvious to the authors as distinct from Résumé: Citheronia maureillei n. -
ISSUE #38, Page 68...72 Pickering + State Coordinators
SOUTHERN LEPIDOPTERISTS’ NEWS VOLUME 38 NO.1 (2016), PG. 67 WHY FLY NOW? PUPA BANKS, APOSEMATISM, AND OTHER FACTORS THAT MAY EXPLAIN OBSERVED MOTH FLIGHT ACTIVITY BY JOHN PICKERING Abstract – This paper addresses factors that affect insect flight activity. It presents a 5-year time series of nightly activity at a site in Clarke County, Georgia for Epimecis hortaria, Tulip-tree Beauty (Geometridae: Ennominae)p Nigetia formosalis, Thin-winged Owlet (Erebidae: Scolecocampinae), and Dryocampa rubicunda, Rosy Maple Moth (Saturniidae: Ceratocampinae). These species exemplify three seasonal flight patterns, here defined as diffuse, synchronized, and complex. I propose that diffuse flight patterns are typical of many cryptic species and that synchronized ones are typical of aposematic species and species restricted by the phenology of their hosts. The complex pattern of D. rubicunda shows variation in when individuals broke pupal diapause and eclosed. Because some insects have pupa banks, similar to seed banks in plants, their observed flights and generations may be decoupled. I caution against using terms such as brood, generation, or voltinism to describe observed seasonal adult activity. Instead, I propose that we use the term flight to describe their activity. _____________________________________ Introduction – Many biotic and abiotic factors interact to affect the seasonal flight activity of moths and our ability to sample them accurately (Tauber et al. 1986p Valtonen et al. 2011). They include processes fundamental to each species’ natural history and life cycle. By what means do they disperse, avoid natural enemies, find mates, lay eggs on or near hosts, avoid natural enemies, and in the grand scheme of things, survive for millions of years beyond the next mega-drought, warming period, and ice age? Science has barely begun to explore the complexity of these questions. -
Moths of North Carolina - Early Draft 1
Notodontidae Datana angusii Angus's Datana Moth 10 9 n=5 8 • • • 7 High Mt. • • • 6 • • N 5 • • •• • u 4 • • 3 • • • m 2 • • b 1 • • 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: 34 • • Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec o 10 • f 9 n=47 • = Sighting or Collection 8 • 7 Low Mt. High counts of: in NC since 2001 F 6 • l 5 11 - Orange - 1992-07-07 = Not seen since 2001 4 • i 3 8 - Franklin - 2013-06-12 g 2 Status Rank h 1 6 - Chatham - 2010-09-23 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 10 10 9 9 t 8 n=49 8 n=37 e 7 Pd 7 CP s 6 6 5 5 4 4 3 3 2 2 1 1 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: Notodontidae SUBFAMILY: Phalerinae TRIBE: TAXONOMIC_COMMENTS: One of 16 species in this genus, all but one of which occurs in North America north of Mexico (Miller et al., 2018). -
Insect Declines in the Anthropocene
EN65CH23_Wagner ARjats.cls December 19, 2019 12:24 Annual Review of Entomology Insect Declines in the Anthropocene David L. Wagner Department of Ecology and Evolutionary Biology, University of Connecticut, Storrs, Connecticut 06269, USA; email: [email protected] Annu. Rev. Entomol. 2020. 65:457–80 Keywords First published as a Review in Advance on insect decline, agricultural intensi!cation, climate change, drought, October 14, 2019 precipitation extremes, bees, pollinator decline, vertebrate insectivores The Annual Review of Entomology is online at ento.annualreviews.org Abstract https://doi.org/10.1146/annurev-ento-011019- Insect declines are being reported worldwide for "ying, ground, and aquatic 025151 lineages. Most reports come from western and northern Europe, where the Copyright © 2020 by Annual Reviews. insect fauna is well-studied and there are considerable demographic data for All rights reserved many taxonomically disparate lineages. Additional cases of faunal losses have been noted from Asia, North America, the Arctic, the Neotropics, and else- where. While this review addresses both species loss and population declines, its emphasis is on the latter. Declines of abundant species can be especially worrisome, given that they anchor trophic interactions and shoulder many Access provided by 73.198.242.105 on 01/29/20. For personal use only. of the essential ecosystem services of their respective communities. A review of the factors believed to be responsible for observed collapses and those Annu. Rev. Entomol. 2020.65:457-480. Downloaded from www.annualreviews.org perceived to be especially threatening to insects form the core of this treat- ment. In addition to widely recognized threats to insect biodiversity, e.g., habitat destruction, agricultural intensi!cation (including pesticide use), cli- mate change, and invasive species, this assessment highlights a few less com- monly considered factors such as atmospheric nitri!cation from the burning of fossil fuels and the effects of droughts and changing precipitation patterns.