Effects of Insecticidal Placement on Non-Target Arthropods in the Peanut Ecosystemt J
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Saltmarsh Caterpillar, Estigmene Acrea (Drury) (Insecta: Lepidoptera: Arctiidae)1 John L
EENY218 Saltmarsh Caterpillar, Estigmene acrea (Drury) (Insecta: Lepidoptera: Arctiidae)1 John L. Capinera2 Distribution The saltmarsh caterpillar, Estigmene acrea (Drury), is a native insect found throughout the United States. Its distribution extends to Central America, and in Canada it has damaged crops in Ontario and Quebec. As a pest, it is most common in the southern United States, particularly the southwest. Description and Life Cycle A generation can be completed in 35 to 40 days under ideal conditions, but most reports from the field suggest about six weeks between generations. The number of generations per year is estimated at one in the northern states to three Figure 1. Adult saltmarsh caterpillars, Estigmene acrea (Drury). to four in the south. Overwintering reportedly occurs in Credits: John L. Capinera, UF/IFAS the mature larval stage, with pupation early in the spring. Saltmarsh caterpillars usually are infrequent early in the season, but may attain high numbers by autumn. Eggs The eggs are nearly spherical in shape, and measure about 0.6 mm in diameter. Initially they are yellow, but soon become grayish in color. Females commonly produce 400 to 1000 eggs in one or more clusters. It is not unusual to find a single egg cluster containing 1200 eggs. Eggs hatch in four to five days. Figure 2. Eggs of the saltmarsh caterpillar, Estigmene acrea (Drury). Credits: John L. Capinera, UF/IFAS 1. This document is EENY218, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date July 2001. Revised March 2013. Reviewed July 2019. Visit the EDIS website at https://edis.ifas.ufl.edu for the currently supported version of this publication. -
Preference for High Concentrations of Plant Pyrrolizidine Alkaloids in the Specialist Arctiid Moth Utetheisa Ornatrix Depends on Previous Experience
Arthropod-Plant Interactions (2013) 7:169–175 DOI 10.1007/s11829-012-9232-1 ORIGINAL PAPER Preference for high concentrations of plant pyrrolizidine alkaloids in the specialist arctiid moth Utetheisa ornatrix depends on previous experience Adam Hoina • Carlos Henrique Zanini Martins • Jose´ Roberto Trigo • Rodrigo Cogni Received: 12 October 2012 / Accepted: 31 October 2012 / Published online: 15 November 2012 Ó Springer Science+Business Media Dordrecht 2012 Abstract Secondary metabolites are one the most per- diet with the high PA concentration, while larvae that were vasive defensive mechanisms in plants. Many specialist pretreated with a high PA diet showed no discrimination herbivores have evolved adaptations to overcome these between future feeding of different PA concentration diets. defensive compounds. Some herbivores can even take We discuss our results using mechanistic and evolutionary advantage of these compounds by sequestering them for approaches. Finally, we discuss how these results have protection and/or mate attraction. One of the most studied important implications on the evolution of plant herbivore specialist insects that sequesters secondary metabolites is interactions and how specialist herbivores may decrease the arctiid moth Utetheisa ornatrix. This species sequesters the levels of chemical defenses on plant populations. pyrrolizidine alkaloids (PAs) from its host plant, the legume Crotalaria spp. The sequestered PAs are used as a Keywords Coevolution Á Crotalaria Á Chemical defense Á predator repellent and as a mating pheromone. We used Diet choice Á Mating choice Á Taste receptors this species to test larval preference for different concen- trations of PAs. We purified PAs from plant material and added them at different concentrations to an artificial diet. -
Lepidoptera: Erebidae, Arctiinae) SHILAP Revista De Lepidopterología, Vol
SHILAP Revista de Lepidopterología ISSN: 0300-5267 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España González, E.; Beccacece, H. M. First record of Dysschema sacrifica (Hübner, [1831]) on Soybean ( Glycine max (L.) Merr) (Lepidoptera: Erebidae, Arctiinae) SHILAP Revista de Lepidopterología, vol. 45, núm. 179, septiembre, 2017, pp. 403-408 Sociedad Hispano-Luso-Americana de Lepidopterología Madrid, España Available in: http://www.redalyc.org/articulo.oa?id=45552790005 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative SHILAP Revta. lepid., 45 (179) septiembre 2017: 403-408 eISSN: 2340-4078 ISSN: 0300-5267 First record of Dysschema sacrifica (Hübner, [1831]) on Soybean ( Glycine max (L.) Merr) (Lepidoptera: Erebidae, Arctiinae) E. González & H. M. Beccacece Abstract The presence of Dysschema sacrifica (Hübner, [1831]) on soybean ( Glycine max (L.) Merr) is reported for the first time. Larvae of this species were found consuming soybean leaves in soybean fields in Córdoba province, Argentina, and were able to complete their life cycle. Characteristics of adults and larvae are provided for rapid identification in the field. Due to the widespread distribution of this species within the region where soybean is more intensively cultivated in South America, we conclude that D. sacrifica is a potential soybean pest. Further studies on infestation frequency, damage levels and control by natural enemies are needed. KEY WORDS: Lepidoptera, Erebidae, Arctiidae, Dysschema sacrifica , soybean, pest, Argentina. Primer registro de Dysschema sacrifica (Hübner, [1831]) en soja ( Glycine max (L.) Merr) (Lepidoptera: Erebidae, Arctiinae) Resumen Se reporta por primera vez la presencia de Dysschema sacrifica (Hübner, [1831]) en soja ( Glycine max (L.) Merr). -
000363920800046.Pdf
UNIVERSIDADE ESTADUAL DE CAMPINAS SISTEMA DE BIBLIOTECAS DA UNICAMP REPOSITÓRIO DA PRODUÇÃO CIENTIFICA E INTELECTUAL DA UNICAMP Versão do arquivo anexado / Version of attached file: Versão do Editor / Published Version Mais informações no site da editora / Further information on publisher's website: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0141480 DOI: 10.1371/journal.pone.0141480 Direitos autorais / Publisher's copyright statement: ©2015 by Public Library of Science. All rights reserved. DIRETORIA DE TRATAMENTO DA INFORMAÇÃO Cidade Universitária Zeferino Vaz Barão Geraldo CEP 13083-970 – Campinas SP Fone: (19) 3521-6493 http://www.repositorio.unicamp.br RESEARCH ARTICLE Feeding on Host Plants with Different Concentrations and Structures of Pyrrolizidine Alkaloids Impacts the Chemical-Defense Effectiveness of a Specialist Herbivore Carlos H. Z. Martins1,2☯, Beatriz P. Cunha3‡, Vera N. Solferini3‡, José R. Trigo1☯* 1 Laboratório de Ecologia Química, Departamento de Biologia Animal, Instituto de Biologia, UNICAMP, Caixa Postal 6109, 13083–970, Campinas, São Paulo, Brazil, 2 Programa de Pós-Graduação em Biologia Funcional e Molecular, Instituto de Biologia, UNICAMP, Caixa Postal 6109, 13084–970, Campinas, São Paulo, Brazil, 3 Departamento de Genética e Evolução, Instituto de Biologia, Unicamp, Caixa Postal 6109, 13083–970, Campinas, São Paulo, Brazil ☯ These authors contributed equally to this work. ‡ These authors also contributed equally to this work. * [email protected] OPEN ACCESS Abstract Citation: Martins CHZ, Cunha BP, Solferini VN, Trigo Sequestration of chemical defenses from host plants is a strategy widely used by herbivo- JR (2015) Feeding on Host Plants with Different rous insects to avoid predation. Larvae of the arctiine moth Utetheisa ornatrix feeding on Concentrations and Structures of Pyrrolizidine Alkaloids Impacts the Chemical-Defense unripe seeds and leaves of many species of Crotalaria (Leguminosae) sequester N-oxides Effectiveness of a Specialist Herbivore. -
Great Lakes Entomologist the Grea T Lakes E N Omo L O G Is T Published by the Michigan Entomological Society Vol
The Great Lakes Entomologist THE GREA Published by the Michigan Entomological Society Vol. 45, Nos. 3 & 4 Fall/Winter 2012 Volume 45 Nos. 3 & 4 ISSN 0090-0222 T LAKES Table of Contents THE Scholar, Teacher, and Mentor: A Tribute to Dr. J. E. McPherson ..............................................i E N GREAT LAKES Dr. J. E. McPherson, Educator and Researcher Extraordinaire: Biographical Sketch and T List of Publications OMO Thomas J. Henry ..................................................................................................111 J.E. McPherson – A Career of Exemplary Service and Contributions to the Entomological ENTOMOLOGIST Society of America L O George G. Kennedy .............................................................................................124 G Mcphersonarcys, a New Genus for Pentatoma aequalis Say (Heteroptera: Pentatomidae) IS Donald B. Thomas ................................................................................................127 T The Stink Bugs (Hemiptera: Heteroptera: Pentatomidae) of Missouri Robert W. Sites, Kristin B. Simpson, and Diane L. Wood ............................................134 Tymbal Morphology and Co-occurrence of Spartina Sap-feeding Insects (Hemiptera: Auchenorrhyncha) Stephen W. Wilson ...............................................................................................164 Pentatomoidea (Hemiptera: Pentatomidae, Scutelleridae) Associated with the Dioecious Shrub Florida Rosemary, Ceratiola ericoides (Ericaceae) A. G. Wheeler, Jr. .................................................................................................183 -
Cosmosoma Myrodora, Scarlet-Bodied Wasp Moth (Lepidoptera: Erebidae) Joseph Mccarthy, Forest Huval, Chris Carlton and Gene Reagan
Pest Management and Insect Identification Series Cosmosoma myrodora, Scarlet-Bodied Wasp Moth (Lepidoptera: Erebidae) Joseph McCarthy, Forest Huval, Chris Carlton and Gene Reagan Description Larvae of the scarlet-bodied wasp moth are light yellow and are entirely covered in long, thin hairs.The The scarlet-bodied wasp moth is a member of the hairs are yellowish-white with black tips mixed with a few family Erebidae.The species is well known for its striking black hairs, giving it a speckled appearance.The head and coloration and Batesian mimicry. Batesian mimicry refers rear part of the body are darker yellow, along with the to a situation where an otherwise harmless animal legs. imitates the coloration and behavior of a dangerous or inedible animal to avoid predation.The adult has a bright The caterpillar of this species constructs a cocoon red thorax, abdomen and legs.The abdomen includes from its larval hairs to protect the pupa within.The eight visible segments.The first four are red with a black cocoon is transparent, yellow and speckled with small stripe down the middle and metallic blue spots on each black spots. segment.The last four segments are black, each with three metallic blue spots (one in the center and two on Life Cycle either side).The wings are clear with black veins and Females lay eggs on hempvine (Mikania cordifolia or a thick black outline.The head is metallic blue, bearing Mikania scandens), the larval host plant.When the larvae large, black eyes and black antennae with white tips.The emerge, they first eat their egg casings before moving on bright coloration, clear wings and bicolored antennae to the plant itself.After about one week under normal give the moth its “wasp-like” appearance.This mimicry summer conditions in Louisiana, larvae build their is most apparent when it is flying.The fast-moving wings cocoons and pupate.The adult moths emerge after about and warning colors are convincing. -
The Food Plants of Some 'Primitive' Pentatomoidea (Hemiptera: Heteroptera)
University of Connecticut OpenCommons@UConn ANSC Articles Department of Animal Science 1988 The food plants of some 'primitive' Pentatomoidea (Hemiptera: Heteroptera). Carl W. Schaefer University of Connecticut, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/ansc_articles Part of the Entomology Commons Recommended Citation Schaefer, Carl W., "The food lp ants of some 'primitive' Pentatomoidea (Hemiptera: Heteroptera)." (1988). ANSC Articles. 9. https://opencommons.uconn.edu/ansc_articles/9 9!E THE FOOD PLANTS OF SOME "PRIWtrTTIVE" PENTATOMOIDEA(HEMIPTERA: HETEROPTERA) CARL W. SCHAEFER Department of Ecotogy and Evolutionar.t Biolog.r, Unit,ersity of Connecticut, Storrs, CT 06268 U.S.A. ,ABSTR.ACT The iood plants of the Cydnidae (Cydninae,Sehirinae, Scaptocorinae, Amnestinae, Garsauriinae, Thau- mastellinae,Parastrachiinae, Corimelaeninae), Plataspidae, Megarididae, Cyrtocoridae, and Lestoniidae, compiled {iom the literature, are discussed.So too are the habitats ofthese insects,most ofwhich live on or are associatedwith the ground. This associationsupports an earlier assertionihat life on the ground was the way of lile o{ the early hemipterans. Most of these groups are polyphagous. However, the Plataspidae feed largely upon legumes, the Scaptocorinaeupon the roots ol Gramineae,some Cydninae also upon legumes,and many Sehirinaeupon members of the advanced dicot subclassAsteridae. Fallen seedsand roots are the preferred plant parts. A group ol mostly small drab shieldbugsappears to be primitive -
Cosmosoma Myrodora, Scarlet-Bodied Wasp Moth (Lepidoptera: Erebidae) Joseph Mccarthy, Forest Huval, Chris Carlton and Gene Reagan
Cosmosoma myrodora, Scarlet-Bodied Wasp Moth (Lepidoptera: Erebidae) Joseph McCarthy, Forest Huval, Chris Carlton and Gene Reagan Description Larvae of the scarlet-bodied wasp moth are light yellow and are entirely covered in long, thin hairs. The The scarlet-bodied wasp moth is a member of the hairs are yellowish-white with black tips mixed with a few family Erebidae. The species is well known for its striking black hairs, giving it a speckled appearance. The head and coloration and Batesian mimicry. Batesian mimicry refers rear part of the body are darker yellow, along with the to a situation where an otherwise harmless animal legs. imitates the coloration and behavior of a dangerous or inedible animal to avoid predation. The adult has a bright The caterpillar of this species constructs a cocoon red thorax, abdomen and legs. The abdomen includes from its larval hairs to protect the pupa within. The eight visible segments. The first four are red with a black cocoon is transparent, yellow and speckled with small stripe down the middle and metallic blue spots on each black spots. segment. The last four segments are black, each with three metallic blue spots (one in the center and two on Life Cycle either side). The wings are clear with black veins and Females lay eggs on hempvine (Mikania cordifolia or a thick black outline. The head is metallic blue, bearing Mikania scandens), the larval host plant. When the larvae large, black eyes and black antennae with white tips. The emerge, they first eat their egg casings before moving on bright coloration, clear wings and bicolored antennae to the plant itself. -
Predatory and Parasitic Lepidoptera: Carnivores Living on Plants
Journal of the Lepidopterists' Society 49(4), 1995, 412-453 PREDATORY AND PARASITIC LEPIDOPTERA: CARNIVORES LIVING ON PLANTS NAOMI E. PIERCE Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts, 02138, USA ABSTRACT. Moths and butterflies whose larvae do not feed on plants represent a decided minority slice of lepidopteran diversity, yet offer insights into the ecology and evolution of feeding habits. This paper summarizes the life histories of the known pred atory and parasitic lepidopteran taxa, focusing in detail on current research in the butterfly family Lycaenidae, a group disproportionately rich in aphytophagous feeders and myr mecophilous habits. More than 99 percent of the 160,000 species of Lepidoptera eat plants (Strong et al. 1984, Common 1990). Plant feeding is generally associated with high rates of evolutionary diversification-while only 9 of the 30 extant orders of insects (Kristensen 1991) feed on plants, these orders contain more than half of the total number of insect species (Ehrlich & Raven 1964, Southwood 1973, Mitter et al. 1988, cf. Labandiera & Sepkoski 1993). Phytophagous species are characterized by specialized diets, with fewer than 10 percent having host ranges of more than three plant families (Bernays 1988, 1989), and butterflies being particularly host plant-specific (e.g., Remington & Pease 1955, Remington 1963, Ehrlich & Raven 1964). This kind of life history specialization and its effects on population structure may have contributed to the diversification of phytophages by promoting population subdivision and isolation (Futuyma & Moreno 1988, Thompson 1994). Many studies have identified selective forces giving rise to differences in niche breadth (Berenbaum 1981, Scriber 1983, Rausher 1983, Denno & McClure 1983, Strong et al. -
Hemiptera: Heteroptera) Revealed by Bayesian Phylogenetic Analysis of Nuclear Rdna Sequences 481-496 75 (3): 481– 496 20.12.2017
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Arthropod Systematics and Phylogeny Jahr/Year: 2017 Band/Volume: 75 Autor(en)/Author(s): Lis Jerzy A., Ziaja Dariusz J., Lis Barbara, Gradowska Paulina Artikel/Article: Non-monophyly of the “cydnoid” complex within Pentatomoidea (Hemiptera: Heteroptera) revealed by Bayesian phylogenetic analysis of nuclear rDNA sequences 481-496 75 (3): 481– 496 20.12.2017 © Senckenberg Gesellschaft für Naturforschung, 2017. Non-monophyly of the “cydnoid” complex within Pentatomoidea (Hemiptera: Heteroptera) revealed by Bayesian phylogenetic analysis of nuclear rDNA sequences Jerzy A. Lis *, Dariusz J. Ziaja, Barbara Lis & Paulina Gradowska Department of Biosystematics, Opole University, Oleska 22, 45-052 Opole, Poland; Jerzy A. Lis * [[email protected]]; Dariusz J. Ziaja [[email protected]]; Barbara Lis [[email protected]]; Paulina Gradowska [[email protected]] — * Corresponding author Accepted 02.x.2017. Published online at www.senckenberg.de/arthropod-systematics on 11.xii.2017. Editors in charge: Christiane Weirauch & Klaus-Dieter Klass Abstract The “cydnoid” complex of pentatomoid families, including Cydnidae, Parastrachiidae, Thaumastellidae, and Thyreocoridae, is morphologi- cally defined by the presence of an array of more or less flattened stout setae (called coxal combs), situated on the distal margin of coxae. These structures, suggested to prevent the coxal-trochanteral articulation from injuries caused by particles of soil, sand or dust, by their nature and function are unknown elsewhere in the Heteroptera. As such, coxal combs were regarded as a synapomorphy of this group of families, and enabled the definition of it as a monophylum. -
The Taxonomic Value of the Metathoracic Wing in the Scutelleridae (Hemiptera: Heteroptera)
AN ABSTRACT OF THE THESIS OF EUNICE CHIZURU AU for theMASTER OF ARTS (Name) (Degree) in ENTOMOLOGY presented onnc0(10-VQAD lq/c,C? (Major) (Date) Title: THE TAXONOMIC VALUE OF THE METATHORACIC WING IN THE SCUTELLERIDAE HETEROPTERA). Abstract approved: Redacted for privacy John D. Lattin Classification based on metathoracic wing venation does not coincide with the existing higher classification of the family Scutel- leridae.The wings of the genera in the Scutellerinae possess a similar general pattern of venation which is quite distinct from that of Eurygasterinae, Odontoscelinae, Odontotarsinae, and Pachy- corinae.The Scutellerinae wings possess three additional characters not found in the other subfamilies: a second secondary vein (present in all of the genera); an antevannal vein (present in three-fourths of the genera), and a Pcu stridulitrum (present in one-half of the genera).Based upon wing venation the genera at present included in the Scutellerinae do not fit into the tribal classification. The wings of the Scutellerinae fell into two natural groups, those with the Pcu stridulitrum and those without it.Those without the Pcu stridulitrum are more generalized than those with it. The four other subfamilies in the Scutelleridae, Eurygasterinae, Odontoscelinae, Odontotarsinae and Pachycorinae, cannot be separated from one another on the basis of the characters associated with the metathoracic wing.However, genera in these taxa could be separated from each other in most cases. The Pachycorinae are very homogeneous and very generalized as a group.Two-thirds of the genera are generalized.The Odonto- scelinae are more heterogeneous and specialized than the Odonto- tarsinae which are either generalized or intermediate-generalized. -
Saltmarsh Caterpillar/Acrea Moth
Colorado Insect of Interest Saltmarsh Caterpillar/Acrea Moth Scientific Name: Estigmene acrea (Drury) Figure 1. Saltmarsh caterpillar crossing highway Order: Lepidoptera (Butterflies, Moths, Skippers) Family: Arctiidae/or Arctiinae of the Noctuidae (Woollybears and Tiger Moths) Identification and Descriptive Features: The caterpillars are densely hairy. Younger stages tend to be predominantly yellowish, but as they age they darken. However, there is wide variation on coloration from orange to nearly black. Indistinct striping may also be present. The adult moths are moderate size with a Figure 2. Adult s of the saltmarsh caterpillar, “acrea wing span of 3.5-4.5 cm. The forewings are moths”. Males on top row, females on bottom row.. white with black spotting. Female moths have yellow-orange hindwings and a generally orange abdomen. Males have white hind wings and an abdomen tipped with white. Distribution in Colorado: Statewide except at the highest elevations. Often locally common in many areas of both western and eastern Colorado. Life History and Habits: The saltmarsh caterpillar survives winter as a full grown larva within a cocoon, hidden amongst leaves and other debris on the soil. Pupation occurs in spring and the adults emerge in late spring. After mating the female lays a series of bright yellow egg masses on leaves over the course of several weeks. Eggs hatch about 4-5 days after being laid. Figure 3. Acrea moth with egg mass. Upon egg hatch the caterpillars originally feed as a group, producing skeletonizing injuries to leaves. As they get older, they individually disperse but continue to feed on leaves for another 3-5 weeks.