Taxonomic Update of the Species of Copitarsia Hampson 1906, (Lepidoptera: Noctuidae: Cuculliinae)

Total Page:16

File Type:pdf, Size:1020Kb

Taxonomic Update of the Species of Copitarsia Hampson 1906, (Lepidoptera: Noctuidae: Cuculliinae) Gayana 67(1): 33-38, 2003 ISSN 0717-652X TAXONOMIC UPDATE OF THE SPECIES OF COPITARSIA HAMPSON 1906, (LEPIDOPTERA: NOCTUIDAE: CUCULLIINAE) ACTUALIZACIÓN TAXONOMICA DE LAS ESPECIES DE COPITARSIA HAMPSON 1906, (LEPIDOPTERA: NOCTUIDAE: CUCULLIINAE) Andrés O. Angulo1 & Tania S. Olivares2 1Departamento de Zoología. Facultad de Ciencias Naturales y Oceanográficas. Universidad de Concepción, Concepción, Chile S.A. Casilla 160-C, Fax 56-41-244805, E-mail: [email protected] 2Casilla 4040 correo 3, Concepción, Chile. E-mail: [email protected] SUMMARY The present work is a catalogue of the species of Copitarsia Hampson, including twenty-one species from North to South America. Two species group are separated taxonomically. They are the species group turbata and the species group incommoda. Also new combinations as well as synonyms for some species are proposed. The genitalia male morphological characters of Copitarsia turbata (Herrich-Schaeffer) y Copitarsia incommoda (Walker) are illustrated. KEYWORDS: Lepidoptera. Noctuidae, Cuculliinae, catalogue, Copitarsia Hampson new combinations, new synony- mous, host plants. RESUMEN En este trabajo se presentan las especies de Copitarsia Hampson, 1906, las que suman veintiuna especies descritas, distribuidas desde América del Norte a Sudamérica. Taxonómicamente se separan dos grupos de especies: uno de ellos es el grupo especie turbata y el otro es el grupo especie incommoda. También se proponen nuevas combinaciones y sinónimos para algunas especies. Se ilustran los caracteres taxonómicos diferenciales de los machos de Copitarsia turbata (Herrich-Schaeffer) y Copitarsia incommoda (Walker). PALABRAS CLAVES: Lepidoptera, Noctuidae, Cuculliinae, catálogo, Copitarsia Hampson, nuebas combinaciones, nuevos sinónimos, plantas hospederas. INTRODUCTION In the Lepidopterorum Catalogue of Poole (1989) Copitarsia Hampson and Cotarsina Species of Copitarsia Hampson are distrib- Koehler were treated separately. Later on, uted from Mexico to the Patagonia. They are Castillo & Angulo (1991) indicated the syn- usually associated to crop of agriculture impor- onymy of these two genera, validating tance, specially in countries such as Colombia - Copitarsia Hampson. Poole (1989) also renomi- where they infest flowers (D. Forero, com. pers. nated C. consueta Walker as C. incommoda 2002)- or Mexico - where they infest cole crops. (Walker). In Chile C. turbata (H-S) was errone- 33 Gayana 67(1), 2003 ously identified as C. consueta (Walker) de Río Blanco (April), Argentina: Mendoza (Feb- (Angulo & Weigert 1975 a y b; Artigas 1972; ruary). Angulo et al. 1990). C. consueta is a valid species presently named C. incommoda (Walker). The rec- 4. C. belenensis (Koehler 1973) n. comb. Argen- ognition of the species through their immature tina: Catamarca, Cuesta de Belén (March). stages is confusing because of color variation of C. belensis (Koehler 1973) (lapsus calamorum) larvae. Hence the need to use morphological char- acters of larvae. Adults are best identified using 5. C. clavata Koehler, 1955. Argentina: Chubut, differences in their in their genitalia structures. Comodoro Rivadavia (December). Chile: Talca: In 1991 Castillo & Angulo reviewed the ge- Pehuenche and La Mina (January and February), nus based on eigth species only. Angulo & Olivares Punta Arenas, Tres Puentes (February and Decem- (1999) added new species. The present work com- ber). piles all available information and re-labels known species. 6. C. fleissiana (Koehler 1958) n. comb. Argen- tina: Neuquén, Limay (November) MATERIALS AND METHODS 7. C. gentiliana (Koehler 1961) n. comb. Argen- tina: Neuquén, Tipiliuke, Loncopue) After the revision of the types of genus Copitarsia of the Koehler Collection located at the 8. C. gracilis (Koehler 1951) n. comb. Argentina: Foundation and Miguel Lillo Institute (FML), the Río Negro. Scientific Collections from the Concepción Uni- C. gracilisoides (Poole 1989) Argentina: Neuquén, versity (UCCC), review of literature and biologi- Paso Flores, n. sin. cal material proceeding from this last institution, the revision of external characters and of the geni- 9. C. humilis (Blanchard 1854). Chile: Santiago, tal armature of the specimens was performed Coquimbo. through the Angulo & Weigert (1977) technique. 10. C. incommoda Walker, 1865. México: Mexico City, Durango, Patzcuaro, Jalapa, Costa Rica: RESULTS Volcán Irazu; Guatemala; Colombia: Bogotá; Perú; Argentina: Mendoza, Neuquén, Esquel, Chubut, After a critical review of the species, the de- Santiago del Estero, Buenos Aires, Comodoro finitive listing of the species is the following, con- Rivadavia. sidering the location and date of collection. C. consueta (Walker 1857) (Junior primary homonimous of Agrotis consueta Walker 1857). C. peruviana (Walker 1865). C. margaritella (Dognin 1916). COPITARSIA HAMPSON 1906 11. C. maxima (Koehler 1961) n. comb. Argen- Copitarsia Hampson 1906, p. 184 tina: Neuquén, San Martín de Los Andes (Decem- Cotarsina Koehler 1951, p. 166 ber), San Luis. 1. C. anatunca Angulo & Olivares 1999. Chile: 12. C. mimica Angulo & Olivares 1999. Argen- Talca, La Mina (February) tina: La Rioja, Punta Balasto (January). 2. C. anguloi Castillo 1991. Chile: Talca, La Mina 13. C. murina Angulo, Olivares & Badilla 2001. (November and December), Chiguayante (Octo- Chile: Talca, La Mina (January, October and De- ber), Angol (September). cember). 3. C. basilinea Koehler 1958. Chile: Cautín, Termas 14. C. naenoides (Butler 1882). Chile: Concepción, 34 Actualización taxonómica de Copitarsia: ANGULO, A. & T. OLIVARES Camino a Bulnes (January, February,October, C. incommoda Walker November, December). Argentina: Tucumán. C. paraturbata Castillo & Angulo Euxoa editae Angulo & Jana-Sáenz, 1982. n. sin. C. turbata (H-S) 15. C. paraturbata Castillo & Angulo 1991. Group of species naenoides: The uncus vertex Chile: Iquique, Mamiña (October) holds dorsally two longitudinal plaques with re- curved indentations; the valve vertex holds a 16. C. patagonica Hampson 1906. Argentina: complete corona and a strong digitus somewhat La Rioja, Punta Balasto, Chubut (January), acute (non spatulate); the vesical base does not Mendoza, San Juan. Chile: Cautín, Termas de Río have indented plaques, but has normal thick splin- Blanco (February). ters. Here are found the other 18 species as fol- lows: 17. C. purilinea (Mabille 1885). Patagonia, Santa Cruz. C. anatunca Angulo & Olivares C. anguloi Castillo 18. C. roseofulva (Koehler 1952) n. comb. Bo- C. basilinea Koehler livia: Oruro C. belenensis (Koehler) C. fleissiana (Koehler) 19. C. sulfurea (Koehler 1973) n. comb. Co- C. clavata Koehler lombia: Santa Fe de Bogotá. Argentina: Mendoza, C. gentiliana (Koehler) Chubut, Covunco, Neuquén (December). C. gracilis (Koehler) C. humilis (Blanchard) 20. C. turbata (H-S 1855). Venezuela. Uruguay. C. maxima (Koehler) Perú (Valle del Ica). Colombia, Costa Rica, Ecua- C. mimica Angulo & Olivares dor, Guatemala. Mexico. C. murina Angulo, Olivares & Badilla Argentina: Rio Negro, Neuquén, Potrerillos, C. naenoides (Butler) Mendoza, Jacanto, Córdoba, La Rioja; Chile: C. patagonica Hampson Concepción (January, July, December), Valdivia C. purilinea (Mabille) (January, March and August), Coihueco (Janu- C. roseofulva (Koehler) (with spatulate digitus) ary), Talca y San Clemente (September), Santiago C. sulfurea (Koehler) (October and November). C. vivax (Koehler) 21. C. vivax Koehler 1951. n. comb. Comodoro Rivadavia, Chubut (December). TAXONOMIC CONSIDERATIONS The Copitarsia genus is defined by the INTERSPECIFIC RELATIONS IN shape of the elongated valves, 5 or 6 times longer COPITARSIA than its medial width, attenuated in the vertex, corona presence, with a well developed ampulla, The 21 known species of Copitarsia where the valve stands out in some species, low Hampson can be found in two group of species, developed clasper and the presence of digitus in accordance to the following characteristics: that varies in shape for each specie, unique un- cus with presence of large or poorly developed Group of species turbata: The uncus vertex is pre- splinters, acute saccus with sharp end, digitiform sented dorsally and in a plain manner, without over- juxta, aedeagus with a corona of splinters sur- lapped or noticeable structures; the valve vertex rounding the base of the aedeagus cover, the fe- does not carry any corona, only 5 or 6 strong male genitalia is characterized by the presence strings; spatulate digitus; the vesical base holds two of corpus and sub globose bursae cervix and the indented lateral plaques, in addition to the normal presence of signa in the corpus bursae formed in thick splinters; here there are 3 species: vertical lines. 35 Gayana 67(1), 2003 Copitarsia incommoda Walker v/s (Walker)) which makes that the identification Copitarsia turbata (Herrich-Shaeffer) for each one of them be very exhaustive. Without any doubt the characters that al- These two species that are frequently lows a reliable and safe identification are the male mixed up because they share some agriculture genitalia characters. crops as host and they look alike in their exter- The knowledge of the immature stages nal appearance. Angulo et al. (1990) makes ref- within the genus is reduced to only two species: erence to the external morphological differences Copitarsia turbata and Copitarsia incommoda. present in both species. Work has been done recently with C. clavata and One of the most important is the, C. the description of its immature stages (Zúniga et incommoda Walker (=Copitarsia consueta al. (in litt.)). TABLE I.
Recommended publications
  • SHILAP Revta. Lepid., 36 (143), Septiembre 2008: 349-409 CODEN: SRLPEF ISSN:0300-5267
    SHILAP Revista de Lepidopterología ISSN: 0300-5267 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España Rodríguez, M. A.; Angulo, A. O. Revisión taxonómica y filogenética del género Scriptania Hampson, 1905 (Lepidoptera: Noctuidae, Hadeninae) SHILAP Revista de Lepidopterología, vol. 36, núm. 143, septiembre, 2008, pp. 349-409 Sociedad Hispano-Luso-Americana de Lepidopterología Madrid, España Disponible en: http://www.redalyc.org/articulo.oa?id=45512164005 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto 349-409 Revisión taxonómica y f 4/9/08 17:40 Página 349 SHILAP Revta. lepid., 36 (143), septiembre 2008: 349-409 CODEN: SRLPEF ISSN:0300-5267 Revisión taxonómica y filogenética del género Scriptania Hampson, 1905 (Lepidoptera: Noctuidae, Hadeninae) M. A. Rodríguez & A. O. Angulo Resumen Se analiza la situación taxonómica del género Scriptania Hampson, 1905. Usando el método de ANGULO & WEIGERT (1977), se obtuvieron las estructuras genitales para efectuar las descripciones y redescripciones de las especies del género Scriptania y la clave de separación para las especies del género. Se hace un análisis filo- genético sobre la base de caracteres morfológicos externos e internos (genitalia del macho y hembra) usando los programas informáticos computacionales Mc Clade 2.1, PAUP 3.0, PAUP 4.0B y Hennig 86, versión 1.5, para co- nocer la historia evolutiva de estas especies resultando Scriptania como un grupo monofilético basado en 14 sina- pomorfías.
    [Show full text]
  • Working List of Prairie Restricted (Specialist) Insects in Wisconsin (11/26/2015)
    Working List of Prairie Restricted (Specialist) Insects in Wisconsin (11/26/2015) By Richard Henderson Research Ecologist, WI DNR Bureau of Science Services Summary This is a preliminary list of insects that are either well known, or likely, to be closely associated with Wisconsin’s original native prairie. These species are mostly dependent upon remnants of original prairie, or plantings/restorations of prairie where their hosts have been re-established (see discussion below), and thus are rarely found outside of these settings. The list also includes some species tied to native ecosystems that grade into prairie, such as savannas, sand barrens, fens, sedge meadow, and shallow marsh. The list is annotated with known host(s) of each insect, and the likelihood of its presence in the state (see key at end of list for specifics). This working list is a byproduct of a prairie invertebrate study I coordinated from1995-2005 that covered 6 Midwestern states and included 14 cooperators. The project surveyed insects on prairie remnants and investigated the effects of fire on those insects. It was funded in part by a series of grants from the US Fish and Wildlife Service. So far, the list has 475 species. However, this is a partial list at best, representing approximately only ¼ of the prairie-specialist insects likely present in the region (see discussion below). Significant input to this list is needed, as there are major taxa groups missing or greatly under represented. Such absence is not necessarily due to few or no prairie-specialists in those groups, but due more to lack of knowledge about life histories (at least published knowledge), unsettled taxonomy, and lack of taxonomic specialists currently working in those groups.
    [Show full text]
  • PHEROMONE TRAP for Monitoring Copitarsia Decolora (LEPIDOPTERA: NOCTUIDAE) ACTIVITY in Cruciferous Crops in Mexico
    602 Florida Entomologist 95(3) September 2012 PHEROMONE TRAP FOR MONITORING COPITARSIA DECOLORA (LEPIDOPTERA: NOCTUIDAE) ACTIVITY IN CRUCIFEROUS CROPS IN MEXICO OVIDIO DIAZ-GOMEZ1, EDI A. MALO2, SARAH A. PATIÑO-ARRELLANO1 AND JULIO C. ROJAS2,* 1Facultad de Agronomía, Universidad Autónoma de San Luis Potosí (UASLP), Álvaro Obregón 64, CP 78000, San Luis Potosí, México 2Departamento de Entomología Tropical, El Colegio de la Frontera Sur (ECOSUR), Carretera Antiguo Aeropuerto km 2.5, CP 30700, Tapachula, Chiapas, México *Corresponding author; Email: [email protected] ABSTRACT Copitarsia decolora (Guenée) is an important pest of several crops such in Mexico, Central and South America. In addition, this species is a regulatory concern in the USA. In this work, we investigated the influence of trap design, trap height, and trap color on pheromone trap catches of C. decolora males in cruciferous crops. Additionally, we investigated the seasonal dynamics of C. decolara for 3 yr. The water-trap captured a significantly higher number of males compared to the jug trap and the Scentry® Heliothis trap. There were no significant differences between in the number of males captured by traps positioned at 0.5, 1, and 1.5 m above ground level. There was also no an interaction between trap design and trap height. Green water-traps captured more males than red water-traps, however, the catches of red water-traps were intermediate and not significantly different from those captured by yellow, blue, and brown water-traps. A total of 6,978 C. decolora males were captured during the 3 yr of trapping. The overall distribution of trap captures over the season was unimodal, with a distinctive peak in trap catches occurring between Mar and Apr.
    [Show full text]
  • Errata and First Update to the 2010 Checklist of the Lepidoptera Of
    Errata and first uppppdate to the 2010 checklist of the Lepidoptera of Alberta Gregory R. Pohl, Jason J Dombroskie, Jean‐François Landry, Charles D Bird, and Vazrick Nazari lead author contact: [email protected] Introduction: Since the Annotated list of the Lepidoptera of Alberta was published in March 2010 (Pohl et al. 2010), a few typographical and nomenclatural errors have come to the authors' attention, as well as three erroneous AB records that were inadvertently omitted from that publication. Additionally, a considerable number of new AB species records have been brought to our attention since that checklist went to press. As expected, most are microlepidoptera. We detail all these items below, in what we hope will be a regular series of addenda to the AB list. If you are aware of further errors or additions to the AB Lepidoptera list, please contact the authors. Wit hin the NidNoctuoidea, there are a few minor iiiinconsistencies in the order of species wihiithin genera, and in the order of genera within tribes or subtribes, as compared to the sequence published by Lafontaine & Schmidt (2010). As well, the sequence of tribes in the AB list does not exactly match that of Lafontaine & Schmidt (2010), particularly in the Erebinae. We are not detailing those minor differences here unless they involve a move to a new genus or new higher taxonomic category. Errata: Abstract, p. 2, line 10, should read "1530... annotations are given" 41 Nemapogon granella (p. 55). Add Kearfott (1905) to the AB literature records. 78 Caloptilia syringella (p. 60). This species should be placed in the genus Gracillaria as per De Prins & De Prins (2005).
    [Show full text]
  • List of Insect Species Which May Be Tallgrass Prairie Specialists
    Conservation Biology Research Grants Program Division of Ecological Services © Minnesota Department of Natural Resources List of Insect Species which May Be Tallgrass Prairie Specialists Final Report to the USFWS Cooperating Agencies July 1, 1996 Catherine Reed Entomology Department 219 Hodson Hall University of Minnesota St. Paul MN 55108 phone 612-624-3423 e-mail [email protected] This study was funded in part by a grant from the USFWS and Cooperating Agencies. Table of Contents Summary.................................................................................................. 2 Introduction...............................................................................................2 Methods.....................................................................................................3 Results.....................................................................................................4 Discussion and Evaluation................................................................................................26 Recommendations....................................................................................29 References..............................................................................................33 Summary Approximately 728 insect and allied species and subspecies were considered to be possible prairie specialists based on any of the following criteria: defined as prairie specialists by authorities; required prairie plant species or genera as their adult or larval food; were obligate predators, parasites
    [Show full text]
  • Tropical Insect Chemical Ecology - Edi A
    TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol.VII - Tropical Insect Chemical Ecology - Edi A. Malo TROPICAL INSECT CHEMICAL ECOLOGY Edi A. Malo Departamento de Entomología Tropical, El Colegio de la Frontera Sur, Carretera Antiguo Aeropuerto Km. 2.5, Tapachula, Chiapas, C.P. 30700. México. Keywords: Insects, Semiochemicals, Pheromones, Kairomones, Monitoring, Mass Trapping, Mating Disrupting. Contents 1. Introduction 2. Semiochemicals 2.1. Use of Semiochemicals 3. Pheromones 3.1. Lepidoptera Pheromones 3.2. Coleoptera Pheromones 3.3. Diptera Pheromones 3.4. Pheromones of Insects of Medical Importance 4. Kairomones 4.1. Coleoptera Kairomones 4.2. Diptera Kairomones 5. Synthesis 6. Concluding Remarks Acknowledgments Glossary Bibliography Biographical Sketch Summary In this chapter we describe the current state of tropical insect chemical ecology in Latin America with the aim of stimulating the use of this important tool for future generations of technicians and professionals workers in insect pest management. Sex pheromones of tropical insectsUNESCO that have been identified to– date EOLSS are mainly used for detection and population monitoring. Another strategy termed mating disruption, has been used in the control of the tomato pinworm, Keiferia lycopersicella, and the Guatemalan potato moth, Tecia solanivora. Research into other semiochemicals such as kairomones in tropical insects SAMPLErevealed evidence of their presence CHAPTERS in coleopterans. However, additional studies are necessary in order to confirm these laboratory results. In fruit flies, the isolation of potential attractants (kairomone) from Spondias mombin for Anastrepha obliqua was reported recently. The use of semiochemicals to control insect pests is advantageous in that it is safe for humans and the environment. The extensive use of these kinds of technologies could be very important in reducing the use of pesticides with the consequent reduction in the level of contamination caused by these products around the world.
    [Show full text]
  • Native Grasses Benefit Butterflies and Moths Diane M
    AFNR HORTICULTURAL SCIENCE Native Grasses Benefit Butterflies and Moths Diane M. Narem and Mary H. Meyer more than three plant families (Bernays & NATIVE GRASSES AND LEPIDOPTERA Graham 1988). Native grasses are low maintenance, drought Studies in agricultural and urban landscapes tolerant plants that provide benefits to the have shown that patches with greater landscape, including minimizing soil erosion richness of native species had higher and increasing organic matter. Native grasses richness and abundance of butterflies (Ries also provide food and shelter for numerous et al. 2001; Collinge et al. 2003) and butterfly species of butterfly and moth larvae. These and moth larvae (Burghardt et al. 2008). caterpillars use the grasses in a variety of ways. Some species feed on them by boring into the stem, mining the inside of a leaf, or IMPORTANCE OF LEPIDOPTERA building a shelter using grass leaves and silk. Lepidoptera are an important part of the ecosystem: They are an important food source for rodents, bats, birds (particularly young birds), spiders and other insects They are pollinators of wild ecosystems. Terms: Lepidoptera - Order of insects that includes moths and butterflies Dakota skipper shelter in prairie dropseed plant literature review – a scholarly paper that IMPORTANT OF NATIVE PLANTS summarizes the current knowledge of a particular topic. Native plant species support more native graminoid – herbaceous plant with a grass-like Lepidoptera species as host and food plants morphology, includes grasses, sedges, and rushes than exotic plant species. This is partially due to the host-specificity of many species richness - the number of different species Lepidoptera that have evolved to feed on represented in an ecological community, certain species, genus, or families of plants.
    [Show full text]
  • A Unified Degree Day Model Describes Survivorship of Copitarsia Corruda
    Bulletin of Entomological Research (2009) 99, 65–72 doi:10.1017/S0007485308006111 Ó 2008 Cambridge University Press Printed in the United Kingdom First published online 12 November 2008 A unified degree day model describes survivorship of Copitarsia corruda Pogue & Simmons (Lepidoptera: Noctuidae) at different constant temperatures N.N. Go´mez1, R.C. Venette2 *, J.R. Gould3 and D.F. Winograd3 1Department of Biology, University of North Dakota, 10 Cornell Street, Stop 9019, Grand Forks, ND 58202, USA: 2USDA, Forest Service, Northern Research Station, 1561 Lindig Street, St. Paul, MN 55108, USA: 3USDA, Animal and Plant Health Inspection Service, Building 1398, Otis ANGB, MA 02542-5008 Abstract Predictions of survivorship are critical to quantify the probability of establish- ment by an alien invasive species, but survival curves rarely distinguish between the effects of temperature on development versus senescence. We report chronological and physiological age-based survival curves for a potentially in- vasive noctuid, recently described as Copitarsia corruda Pogue & Simmons, collected from Peru and reared on asparagus at six constant temperatures between 9.7 and 34.5C. Copitarsia spp. are not known to occur in the United States but are routinely intercepted at ports of entry. Chronological age survival curves differ significantly among temperatures. Survivorship at early age after hatch is greatest at lower temperatures and declines as temperature increases. Mean longevity was 220 (+13 SEM) days at 9.7C. Physiological age survival curves constructed with developmental base temperature (7.2C) did not correspond to those constructed with a senescence base temperature (5.9C). A single degree day survival curve with an appropriate temperature threshold based on senescence adequately describes survivorship under non-stress temperature conditions (5.9–24.9C).
    [Show full text]
  • Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
    ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4.
    [Show full text]
  • Libro Manejo De Plagas En Trigo Y Cebada
    C M Y CM MY CY CMY K Manejo de plagas en trigo y cebada Adela Ribeiro • Horacio Silva • Silvana Abbate Manejo de plagas en trigo y cebada bibliotecaplural La publicación de este libro fue realizada con el apoyo de la Comisión Sectorial de Investigación Científica (csic) de la Universidad de la República. Los libros publicados en la presente colección han sido evaluados por académicos de reconocida trayectoria, en las temáticas respectivas. La Subcomisión de Apoyo a Publicaciones de la csic, integrada por Luis Bértola, Carlos Demasi, Fernando Miranda y Liliana Carmona, ha sido la encargada de recomendar los evaluadores para la convocatoria 2013. © Adela Ribeiro, Horacio Silva, Silvana Abbate, 2013 © Universidad de la República, 2014 Ediciones universitarias, Unidad de Comunicación de la Universidad de la República (ucur) 18 de Julio 1824 (Facultad de Derecho, subsuelo Eduardo Acevedo) Montevideo, cp 11200, Uruguay Tels.: (+598) 2408 5714 - (+598) 2408 2906 Telefax: (+598) 2409 7720 Correo electrónico: <[email protected]> <www.universidad.edu.uy/bibliotecas/dpto_publicaciones.htm> isbn: 978-9974-0-1138-0 Contenido Presentación de la Colección Biblioteca Plural, Rodrigo Arocena ........................9 Introducción .............................................................................................................................................................11 Insectos del suelo ................................................................................................................................................13
    [Show full text]
  • Lepidoptera: Noctuidae) Captured in Traps Baited with (Z)-11-Hexadecenal
    Early spring moths (Lepidoptera: Noctuidae) captured in traps baited with (Z)-11-hexadecenal Peter J. Landolt1,*, Dane Elmquist1,2, and Richard S. Zack2 Moth sex pheromones are relatively specific; their attractiveness is Vaportape (Hercon Environmental Inc., Emigsville, Pennsylvania, USA) limited to 1 or a few species. Such specificity is achieved in part by the was put in the trap bucket to kill captured insects. Baited and unbaited diversity of chemical structures found as pheromones, and with com- traps were placed about 10 m apart at field sites, with 1 pair of traps binations or blends of these compounds (Mayer & McLaughlin 1991). per site. Replicates of paired traps were placed > 2 km apart. The 32 Specificity of sex pheromones is important for the maintenance of re- trap sites, each with a pair of baited and unbaited traps, were in un- productive isolation, and prevention of mating mistakes among species cultivated riparian habitats. Trap site locations are provided in Table 1. of moths (e.g., Greenfield & Karandinos 1979; Roelofs & Carde 1974). Traps were operated in Mar and Apr of 2016 and 2017 (Table 1). Traps Specificity is also an important attribute of sex pheromones or sex were checked and captured insects removed weekly. Lures and Vapor- attractants when used as lures for monitoring pest moths. However, tape were replaced at 4 wk. when non-target moths are captured in monitoring traps deployed for For each species, numbers of moths caught were summed for each a particular pest species, trap-checking is more difficult and misidenti- trap over the course of the trap placement.
    [Show full text]
  • The Genus Dargida Walker, 1856 (Lepidoptera: Noctuidae) in Louisiana
    The genus Dargida Walker, 1856 (Lepidoptera: Noctuidae) in Louisiana by Vernon Antoine Brou Jr., 74320 Jack Loyd Road, Abita Springs, Louisiana 70420 email: [email protected] a b c Fig 1. Dargida rubripennis: a. male, b. female. Dargida diffusa: c. male. The genera Faronta Smith, 1908 and Strigania Hampson, 1905 were synonymized under the genus Dargida Walker, 1856 by (Rodríguez and Angulo, 2005). In their revision, these authors listed 53 species of Dargida, creating fourteen new combinations and listing new records. In America, north of Mexico, eight 18 Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 9 0 number of adults Fig 2. Adult D. rubripennis captured at sec.24T6SR12E, 4.2 mi. NE of Abita Springs, Louisiana. n = 212 species are assigned to the genus Dargida. I have taken only two species of the genus in Louisiana: Dargida rubripennis (Grote & Robinson, 1870) (Fig. D. rubripennis D. diffusa 1a,b) and Dargida diffusa (Walker, 1856) (Fig. 1c.) Both species were previously reported for Louisiana, with adults captured during the month of September using ultraviolet light traps (Chapin and Callahan, 1967). Fig 3. Parish records for D. rubripennis and D. diffusa by this author. Within Louisiana, four adults of diffusa were captured on four separate occasions, once by Chapin and Callahan, and on three occasions (May and October) by this author. The type locality for diffusa is Nova Scotia, Canada. Covell listed the range for diffusa to include New Foundland to Virginia, west through Canada, south to Texas during the months of April through October in two to three broods.
    [Show full text]