Vegetable Pests: European Corn Borer W
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Efficacy of Pheromones for Managing of the Mediterranean Flour Moth
12th International Working Conference on Stored Product Protection (IWCSPP) in Berlin, Germany, October 7-11, 2018 HOSSEININAVEH, V., BANDANI, A.R., AZMAYESHFARD, P., HOSSEINKHANI, S. UND M. KAZZAZI, 2007. Digestive proteolytic and amylolytic activities in Trogoderma granarium Everts (Dermestidae: Coleoptera). J. Stored Prod. Res., 43: 515-522. ISHAAYA, I. UND R. HOROWITZ, 1995. Pyriproxyfen, a novel insect growth regulator for controlling whiteflies. Mechanism and resistance management. Pestic. Sci., 43: 227–232. ISHAAYA, I., BARAZANI, A., KONTSEDALOV, S. UND A.R. HOROWITZ, 2007. Insecticides with novel mode of action: Mechanism, selectivity and cross-resistance. Entomol. Res., 37: 148-152. IZAWA, Y., M. UCHIDA, T. SUGIMOTO AND T. ASAI, 1985. Inhibition of Chitin Biosynthesis by buprofezin analogs in relation to their activity controlling Nilaparvata lugens. Pestic. Biochem. Physiol., 24: 343-347. KLJAJIC, P. UND I. PERIC, 2007. Effectiveness of wheat-applied contact insecticide against Sitophilus granarius (L.) originating from different populations. J. Stored Prod. Res., 43: 523-529. KONNO, T., 1990. Buprofezin: A reliable IGR for the control of rice pests. Soci. Chem. Indus., 23: 212 - 214. KOSTYUKOVSKY, M. UND A. TROSTANETSKY, 2006. The effect of a new chitin synthesis inhibitor, novaluron, on various developmental stages ofTribolium castaneum (Herbst). J. Stored Prod. Res., 42: 136-148. KOSTYUKOVSKY, M., CHEN, B., ATSMI, S. UND E. SHAAYA, 2000. Biological activity of two juvenoids and two ecdysteroids against three stored product insects. Insect Biochem. Mol. Biol., 30: 891-897. LIANG, P., CUI, J.Z., YANG, X.Q. UND X.W. GAO, 2007. Effects of host plants on insecticide susceptibility and carboxylesterase activity in Bemisia tabaci biotype B and greenhouse whitefly, Trialeurodes vaporariorum. -
European Corn Borer, Ostrinia Nubilalis (Hübner) (Insecta: Lepidoptera: Crambidae)1 John L
EENY156 European Corn Borer, Ostrinia nubilalis (Hübner) (Insecta: Lepidoptera: Crambidae)1 John L. Capinera2 Distribution flights and oviposition typically occur in May, late June, and August. In locations with four generations, adults are active First found in North America near Boston, Massachusetts in April, June, July, and August-September. in 1917, European corn borer, Ostrinia nubilalis (Hübner), now has spread as far west as the Rocky Mountains in both Egg Canada and the United States, and south to the Gulf Coast Eggs are deposited in irregular clusters of about 15 to 20. states. European corn borer is thought to have originated in The eggs are oval, flattened, and creamy white in color, Europe, where it is widespread. It also occurs in northern usually with an iridescent appearance. The eggs darken Africa. The North American European corn borer popula- to a beige or orangish tan color with age. Eggs normally tion is thought to have resulted from multiple introductions are deposited on the underside of leaves, and overlap like from more than one area of Europe. Thus, there are at least shingles on a roof or fish scales. Eggs measure about 1.0 two, and possibly more, strains present. This species occurs mm in length and 0.75 m in width. The developmental infrequently in Florida. threshold for eggs is about 15°C. Eggs hatch in four to nine days. Life Cycle and Description The number of generations varies from one to four, with only one generation occurring in northern New England and Minnesota and in northern areas of Canada, whereas three to four generations occur in Virginia and other southern locations. -
Tachinidae, Tachinid Flies
Beneficial Insects Class Insecta, Insects Order Diptera, Flies, gnats, and midges Diptera means “two wings,” and true flies bear only one pair of functional wings. Flies are one of the largest insect groups, with approximately 35 families that contain predatory or parasitic species. All flies have piercing/sucking/sponging mouthparts. Tachinid flies Family Tachinidae Description and life history: This is a large and important family, with up to 1300 native parasitoid species in North America and additional introduced species to help control foreign pests. These flies vary in color, size, and shape but most resemble houseflies. Adults are usually gray, black, or striped, and hairy. Adults lay eggs on plants to be consumed by hosts, or they glue eggs to the outside of hosts, so the maggots can burrow into the host. Rarely will tachinids insert eggs into host bodies. Tachinid flies develop rapidly within their host and pupate in 4–14 days. By the time they emerge, they have killed their host. Many species have several generations a year, although some are limited by hosts with a single annual generation. Prey species: Most tachinid flies attack caterpillars and adult and larval beetles, although others specialize on Tachinid fly adult. (327) sawfly larvae, true bugs, grasshoppers, or other insects. Photo: John Davidson Lydella thompsoni is a parasitoid of European corn borer, Voria ruralis attacks cabbage looper caterpillars, Myiopharus doryphorae attacks Colorado potato beetle larvae, and Istocheta aldrichi parasitizes adult Japanese beetles. Although these are very important natural en- emies, none is available commercially. IPM of Midwest Landscapes 263. -
Twenty-Five Pests You Don't Want in Your Garden
Twenty-five Pests You Don’t Want in Your Garden Prepared by the PA IPM Program J. Kenneth Long, Jr. PA IPM Program Assistant (717) 772-5227 [email protected] Pest Pest Sheet Aphid 1 Asparagus Beetle 2 Bean Leaf Beetle 3 Cabbage Looper 4 Cabbage Maggot 5 Colorado Potato Beetle 6 Corn Earworm (Tomato Fruitworm) 7 Cutworm 8 Diamondback Moth 9 European Corn Borer 10 Flea Beetle 11 Imported Cabbageworm 12 Japanese Beetle 13 Mexican Bean Beetle 14 Northern Corn Rootworm 15 Potato Leafhopper 16 Slug 17 Spotted Cucumber Beetle (Southern Corn Rootworm) 18 Squash Bug 19 Squash Vine Borer 20 Stink Bug 21 Striped Cucumber Beetle 22 Tarnished Plant Bug 23 Tomato Hornworm 24 Wireworm 25 PA IPM Program Pest Sheet 1 Aphids Many species (Homoptera: Aphididae) (Origin: Native) Insect Description: 1 Adults: About /8” long; soft-bodied; light to dark green; may be winged or wingless. Cornicles, paired tubular structures on abdomen, are helpful in identification. Nymph: Daughters are born alive contain- ing partly formed daughters inside their bodies. (See life history below). Soybean Aphids Eggs: Laid in protected places only near the end of the growing season. Primary Host: Many vegetable crops. Life History: Females lay eggs near the end Damage: Adults and immatures suck sap from of the growing season in protected places on plants, reducing vigor and growth of plant. host plants. In spring, plump “stem Produce “honeydew” (sticky liquid) on which a mothers” emerge from these eggs, and give black fungus can grow. live birth to daughters, and theygive birth Management: Hide under leaves. -
Big Creek Lepidoptera Checklist
Big Creek Lepidoptera Checklist Prepared by J.A. Powell, Essig Museum of Entomology, UC Berkeley. For a description of the Big Creek Lepidoptera Survey, see Powell, J.A. Big Creek Reserve Lepidoptera Survey: Recovery of Populations after the 1985 Rat Creek Fire. In Views of a Coastal Wilderness: 20 Years of Research at Big Creek Reserve. (copies available at the reserve). family genus species subspecies author Acrolepiidae Acrolepiopsis californica Gaedicke Adelidae Adela flammeusella Chambers Adelidae Adela punctiferella Walsingham Adelidae Adela septentrionella Walsingham Adelidae Adela trigrapha Zeller Alucitidae Alucita hexadactyla Linnaeus Arctiidae Apantesis ornata (Packard) Arctiidae Apantesis proxima (Guerin-Meneville) Arctiidae Arachnis picta Packard Arctiidae Cisthene deserta (Felder) Arctiidae Cisthene faustinula (Boisduval) Arctiidae Cisthene liberomacula (Dyar) Arctiidae Gnophaela latipennis (Boisduval) Arctiidae Hemihyalea edwardsii (Packard) Arctiidae Lophocampa maculata Harris Arctiidae Lycomorpha grotei (Packard) Arctiidae Spilosoma vagans (Boisduval) Arctiidae Spilosoma vestalis Packard Argyresthiidae Argyresthia cupressella Walsingham Argyresthiidae Argyresthia franciscella Busck Argyresthiidae Argyresthia sp. (gray) Blastobasidae ?genus Blastobasidae Blastobasis ?glandulella (Riley) Blastobasidae Holcocera (sp.1) Blastobasidae Holcocera (sp.2) Blastobasidae Holcocera (sp.3) Blastobasidae Holcocera (sp.4) Blastobasidae Holcocera (sp.5) Blastobasidae Holcocera (sp.6) Blastobasidae Holcocera gigantella (Chambers) Blastobasidae -
No Slide Title
Tachinidae: The “other” parasitoids Diego Inclán University of Padova Outline • Briefly (re-) introduce parasitoids & the parasitoid lifestyle • Quick survey of dipteran parasitoids • Introduce you to tachinid flies • major groups • oviposition strategies • host associations • host range… • Discuss role of tachinids in biological control Parasite vs. parasitoid Parasite Life cycle of a parasitoid Alien (1979) Life cycle of a parasitoid Parasite vs. parasitoid Parasite Parasitoid does not kill the host kill its host Insects life cycles Life cycle of a parasitoid Some facts about parasitoids • Parasitoids are diverse (15-25% of all insect species) • Hosts of parasitoids = virtually all terrestrial insects • Parasitoids are among the dominant natural enemies of phytophagous insects (e.g., crop pests) • Offer model systems for understanding community structure, coevolution & evolutionary diversification Distribution/frequency of parasitoids among insect orders Primary groups of parasitoids Diptera (flies) ca. 20% of parasitoids Hymenoptera (wasps) ca. 70% of parasitoids Described Family Primary hosts Diptera parasitoid sp Sciomyzidae 200? Gastropods: (snails/slugs) Nemestrinidae 300 Orth.: Acrididae Bombyliidae 5000 primarily Hym., Col., Dip. Pipunculidae 1000 Hom.:Auchenorrycha Conopidae 800 Hym:Aculeata Lep., Orth., Hom., Col., Sarcophagidae 1250? Gastropoda + others Lep., Hym., Col., Hem., Tachinidae > 8500 Dip., + many others Pyrgotidae 350 Col:Scarabaeidae Acroceridae 500 Arach.:Aranea Hym., Dip., Col., Lep., Phoridae 400?? Isop.,Diplopoda -
Life Table of Orius Insidiosus (Hemiptera: Anthocoridae) Feeding on Sitotroga Cerealella (Lepidoptera: Gelechiidae) Eggs
Research article http://www.revistas.unal.edu.co/index.php/refame Life table of Orius insidiosus (Hemiptera: Anthocoridae) feeding on Sitotroga cerealella (Lepidoptera: Gelechiidae) eggs Tabla de vida de Orius insidiosus (Hemiptera: Anthocoridae) alimentado con huevos de Sitotroga cerealella (Leideoptera: Gelechiidae) doi: 10.15446/rfna.v69n1.54745 Jhon Alexander Avellaneda Nieto1, Fernando Cantor Rincon1, Daniel Rodríguez Caicedo1* ABSTRACT Key words: To use a natural enemy to control an insect pest, it is important to determine the biological parameters Biological control of the native populations of the predator. The goal of this study was determinate the biological Pirate bugs parameters of O. insidiosus fed on Sitotroga cerealella eggs. A batch of 225 O. insidiosus eggs were Stock colony laid into bean pods. The bean pods were kept in glass jars, and the eggs and first instar nymphs were Sabana de Bogotá counted daily. All nymphs were extracted and individualized in Petri dishes. The presence/absence of exuvie was observed daily as a way to assess the emergence of adults from the nymphal stage. Seventeen adult couples were placed into Petri dishes with a segment of bean pod. The bean pod segments were extracted and replaced daily, counting the number of eggs present on the pods. The life cycle, survival percentage, sex ratio, male/female longevity, pre ovoposition, ovoposition and post ovoposition periods were determined. Finally, fertility life table parameters were estimated. The nymphal development time was 12.0 ± 0.22 days, with 80.47% ± 3.23 survival, while the total development time was 15.0 ± 0.23 days, with 66.67% ± 1.90 survival. -
Phylogeny and Evolution of Lepidoptera
EN62CH15-Mitter ARI 5 November 2016 12:1 I Review in Advance first posted online V E W E on November 16, 2016. (Changes may R S still occur before final publication online and in print.) I E N C N A D V A Phylogeny and Evolution of Lepidoptera Charles Mitter,1,∗ Donald R. Davis,2 and Michael P. Cummings3 1Department of Entomology, University of Maryland, College Park, Maryland 20742; email: [email protected] 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560 3Laboratory of Molecular Evolution, Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland 20742 Annu. Rev. Entomol. 2017. 62:265–83 Keywords Annu. Rev. Entomol. 2017.62. Downloaded from www.annualreviews.org The Annual Review of Entomology is online at Hexapoda, insect, systematics, classification, butterfly, moth, molecular ento.annualreviews.org systematics This article’s doi: Access provided by University of Maryland - College Park on 11/20/16. For personal use only. 10.1146/annurev-ento-031616-035125 Abstract Copyright c 2017 by Annual Reviews. Until recently, deep-level phylogeny in Lepidoptera, the largest single ra- All rights reserved diation of plant-feeding insects, was very poorly understood. Over the past ∗ Corresponding author two decades, building on a preceding era of morphological cladistic stud- ies, molecular data have yielded robust initial estimates of relationships both within and among the ∼43 superfamilies, with unsolved problems now yield- ing to much larger data sets from high-throughput sequencing. Here we summarize progress on lepidopteran phylogeny since 1975, emphasizing the superfamily level, and discuss some resulting advances in our understanding of lepidopteran evolution. -
International Symposium on Biological Control of Arthropods 2005
Agusti et al. _________________________________________________________________________ Session 12: Environmental Risk Assessment of Invertebrate Biological Control Agents ESTIMATING PARASITISM LEVELS IN OSTRINIA NUBILALIS HÜBNER (LEPIDOPTERA: CRAMBIDAE) FIELD POPULATIONS USING MOLECULAR TECHNIQUES Nuria AGUSTI1, Denis BOURGUET2, Thierry SPATARO3, and Roger ARDITI3 1Dept. de Proteccio Vegetal Institut de Recerca i Tecnologia Agroalimentaries (IRTA) 08348 Cabrils (Barcelona), Spain [email protected] 2Centre de Biologie et de Gestion des Populations (CBGP) Institut National de la Recherche Agronomique (INRA) Campus International de Baillarguet CS 30 016, 34988 Montferrier / Lez cedex, France [email protected] 3Ecologie des populations et communautés 76 Institut National Agronomique Paris-Grignon (INA P-G) 75231 Paris cedex 05, France [email protected] [email protected] Accurate detection and identification of parasitoids are critical to the success of IPM pro- grams to detect unusual variations of the density of these natural enemies, which may follow changes in agricultural practices. For such purposes specific molecular markers to detect Lydella thompsoni (Herting) and Pseudoperichaeta nigrolineata (Walker) (Diptera: Tachinidae) within the european corn borer, Ostrinia nubilalis (Hübner) (Lepidoptera: Crambidae) have been developed. Primers amplifying fragments of the mitochondrial cytochrome oxidase I (COI) gene were designed following alignment of comparable sequences for a range of parasitoid and host species. Each of the primer pairs proved to be species-specific to one of those ta- chinid species, amplifying DNA fragments of 191 and 91 bp in length for L. thompsoni and P. nigrolineata, respectively. This DNA-based technique allowed to perform a molecular detec- tion of parasitism in natural populations of O. nubilalis. Molecular evaluation of parasitism was compared with the traditional method of rearing ECB populations in controlled conditions before breaking off the diapause. -
Orius Insidiosus (Say) and ENTOMOPATHOGENS AS POSSIBLE BIOLOGICAL CONTROL AGENTS for THRIPS
Orius insidiosus (Say) AND ENTOMOPATHOGENS AS POSSIBLE BIOLOGICAL CONTROL AGENTS FOR THRIPS Ronald D. Oetting and Ramona J. Beshear Department of Entomology University of Georgia College of Agriculture, Experiment Stations Georgia Station Griffin, Georgia USA The entomology program in ornamental floriculture at the University of Georgia places primary emphasis on commercial production of flowering and foliage plants under greenhouse conditions. Thrips management is a major part of that program. Several species of foliage and flower inhabiting species are pests on greenhouse crops. The western flower thrips, Frankliniella occidentalis (Pergande), has become the most important pest of the thrips complex during this decade. Other thrips species have also become more difficult to control or occur more frequently on greenhouse crops in different areas of the country. The subject of this paper is the potential use of natural enemies for the management of thrips under greenhouse and other environments. The use of predatory mites for thrips management is discussed in the previous paper and we will focus on two other potential natural enemies: entomopathogens and a hemipteran predator in the genus Orius. Neither of these natural enemies have been utilized in commercial programs for thrips control in greenhouses in the United States but both occur as natural enemies limiting populations of thrips in their respective environments. They should both be considered as potential tools for thrips management. Entomopathogens Entomopathogens are organisms utilized for management of insect populations and the fungi are the only group of pathogens which have been studied for thrips control. There have been three genera of fungi reported from thrips: Verticillium, Entomophthora, and Paecilomyces. -
Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation
CHAPTER THIRTEEN Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation MARJORIE A. LIÉNARD and CHRISTER LÖFSTEDT INTRODUCTION Role of antagonists as enhancers of reproductive isolation and interspecific interactions THE EVOLUTION TOWARDS SPECIALIZED HOST-PLANT ASSOCIATIONS SUMMARY: AN EMERGING MODEL SYSTEM IN RESEARCH ON THE ROLE OF SEX PHEROMONES IN SPECIATION—TOWARD A NEW SEX PHEROMONES AND OTHER ECOLOGICAL FACTORS “SMALL ERMINE MOTH PROJECT”? INVOLVED IN REPRODUCTIVE ISOLATION Overcoming the system limitations Overview of sex-pheromone composition Possible areas of future study Temporal and behavioral niches contributing to species separation ACKNOWLEDGMENTS PHEROMONE BIOSYNTHESIS AND MODULATION REFERENCES CITED OF BLEND RATIOS MALE PHYSIOLOGICAL AND BEHAVIORAL RESPONSE Detection of pheromone and plant compounds Introduction onomic investigations were based on examination of adult morphological characters (e.g., wing-spot size and color, geni- Small ermine moths belong to the genus Yponomeuta (Ypo- talia) (Martouret 1966), which did not allow conclusive dis- nomeutidae) that comprises about 75 species distributed glob- crimination of all species, leading to recognition of the so- ally but mainly in the Palearctic region (Gershenson and called padellus-species complex (Friese 1960) which later Ulenberg 1998). These moths are a useful model to decipher proved to include five species (Wiegand 1962; Herrebout et al. the process of speciation, in particular the importance of eco- 1975; Povel 1984). logical adaptation driven by host-plant shifts and the utiliza- In the 1970s, “the small ermine moth project” was initiated tion of species-specific pheromone mating-signals as prezy- to include research on many aspects of the small ermine gotic reproductive isolating mechanisms. -
Lydella Slavonica, a New Species from the Western Palaearctic with Notes on the Subgenus Lydelloxenis (Diptera, Tachinidae) Theo Zeegers
Tijdschrift voor Entomologie 156 (2013) 103–112 brill.com/tve Lydella slavonica, a new species from the western Palaearctic with notes on the subgenus Lydelloxenis (Diptera, Tachinidae) Theo Zeegers Lydella (Lydelloxenis) slavonica sp. n. is described from Montenegro and Poland. The definition of the subgenus Lydelloxenis Mesnil, 1956 is discussed. A key to western Palaearctic subgenera of Lydella Robineau-Desvoidy, 1830 and species of Lydelloxenis is provided. A phylogenetic analysis for the genus Lydella is provided. The species from the tropics and subtropics are found to form a monophyletic group, called the Metoposisyrops-clade. The species of this clade combined with those of Lydelloxenis are found to form a monophyletic group as well. The results are weakly supported. For practical reasons and nomenclatural stability, Lydelloxenis and Metoposisyrops Townsend, 1916 are proposed as subgenera. Keywords: parasitoids, stem boring caterpillars, phylogeny, Exoristinae, Eryciini. Theo Zeegers, Eikenlaan 24, 3768 EV Soest, the Netherlands. [email protected] Introduction Within the western Palaearctic, the genus Lydella The genus Lydella Robineau-Desvoidy, 1830 is consists of grey tachinids of medium size. The genus known from all major biogeographic regions (O’Ha- is characterized by the bare eye, the erect apical ra 2010). As currently understood, it includes the scutellar setae, presence of one very strong setula subjective synonyms Lydelloxenis Mesnil, 1956 from at base of vein R4+5 and the presence of median the Palaearctic region (Herting 1959) and Dia- discal setae on tergites 3 and 4 (Tschorsnig & Richter traeophaga Towsend, 1916, Metagonistylum Town- 1998). Six species are known (Herting 1984), falling send, 1927 and Metoposisyrops Townsend, 1916 from into two distinct groups.