Fall Armyworm, Spodoptera Frugiperda (JE Smith)
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Egyptian Cottonworm Spodoptera Littoralis
Michigan State University’s invasive species factsheets Egyptian cottonworm Spodoptera littoralis The Egyptian cottonworm is a highly polyphagous defoliator of many cultivated plants. Its accidental introduction to Michigan may be a particular concern to vegetable, fruit and ornamental industries. Michigan risk maps for exotic plant pests. Other common names African cotton leafworm, Egyptian cotton leafworm, Mediterranean Brocade moth Systematic position Insecta > Lepidoptera > Noctuidae > Spodoptera littoralis (Boisduval) Global distribution Adult. (Photo: O. Heikinheimo, Bugwood.org) Most parts of Africa. Southern or Mediterranean Europe: Greece, Italy, Malta, Portugal, Spain. Middle East: Israel, Syria, Turkey. Quarantine status The Egyptian cottonworm has been intercepted at least 65 times at U.S. ports of entry since 2004 (Ellis 2004). This insect has been detected in greenhouses in Ohio but was subsequently eradicated (Passoa 2008). It is listed as an exotic organism of high invasive risk to the United States (USDA-APHIS 2008). Plant hosts Larva. (Photo: Biologische Bundesanstalt für Land- und Forstwirtschaft Archive, A wide host range of at least 87 plant species over Biologische Bundesanstalt für Land- und Forstwirtschaft, Bugwood.org) 40 plant families including many vegetable, fruit and ornamental crops. Some examples include alfalfa, white oblique bands; hind wings pale with brown margins. apples, avocados, beets, bell peppers, cabbage, carrots, Larva: Body up to 45 mm long and hairless; newly cauliflower, cereal, clover, corn, cotton, cucurbits, hatched larvae are blackish-grey to dark green; mature eggplants, figs, geraniums, grapes, lettuce, oaks, okra, larvae are reddish-brown or whitish-yellow; larvae have onions, peas, peanuts, pears, pines, poplars, potatoes, dark and light longitudinal bands and two dark, semi- radish, roses, soybeans, spinach, sunflowers, taro, tea, circular spots on their back. -
Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence
When the Body Hides the Ancestry: Phylogeny of Morphologically Modified Epizoic Earwigs Based on Molecular Evidence Petr Kocarek1*, Vaclav John2, Pavel Hulva2,3 1 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Ostrava, Czech Republic, 2 Department of Zoology, Faculty of Science, Charles University in Prague, Prague, Czech Republic, 3 Life Science Research Centre, Faculty of Science, University of Ostrava, Ostrava, Czech Republic Abstract Here, we present a study regarding the phylogenetic positions of two enigmatic earwig lineages whose unique phenotypic traits evolved in connection with ectoparasitic relationships with mammals. Extant earwigs (Dermaptera) have traditionally been divided into three suborders: the Hemimerina, Arixeniina, and Forficulina. While the Forficulina are typical, well-known, free-living earwigs, the Hemimerina and Arixeniina are unusual epizoic groups living on molossid bats (Arixeniina) or murid rodents (Hemimerina). The monophyly of both epizoic lineages is well established, but their relationship to the remainder of the Dermaptera is controversial because of their extremely modified morphology with paedomorphic features. We present phylogenetic analyses that include molecular data (18S and 28S ribosomal DNA and histone-3) for both Arixeniina and Hemimerina for the first time. This data set enabled us to apply a rigorous cladistics approach and to test competing hypotheses that were previously scattered in the literature. Our results demonstrate that Arixeniidae and Hemimeridae belong in the dermapteran suborder Neodermaptera, infraorder Epidermaptera, and superfamily Forficuloidea. The results support the sister group relationships of Arixeniidae+Chelisochidae and Hemimeridae+Forficulidae. This study demonstrates the potential for rapid and substantial macroevolutionary changes at the morphological level as related to adaptive evolution, in this case linked to the utilization of a novel trophic niche based on an epizoic life strategy. -
Molecular Characterization of Fall Armyworm (Spodoptera Frugiperda) Resistant to Vip3aa20 Protein Expressed in Corn
Molecular Characterization of Fall Armyworm (Spodoptera frugiperda) Resistant to Vip3Aa20 Protein Expressed in Corn Dissertation Presented in partial fulfillment of the requirements for the degree of doctor of philosophy in the Graduate School of The Ohio State University Julio Cesar Fatoretto, B. Sc. Graduate Program in Translational Plant Science The Ohio State University 2017 Dissertation Committee: Andrew P. Michel, Advisor Marcio C. Silva Filho Thomas Mitchell Fernando Consoli Copyright by Julio Cesar Fatoretto 2017 Abstract Transgenic plants containing genes from Bacillus thuringiensis have been used as an alternative to chemical insecticides for insect pest control. The vegetative insecticidal proteins (Vip) secreted during the vegetative growth phase of bacteria are considered a second generation of insecticidal proteins since they do not share any structural or sequence homology with previously used crystal proteins (Cry) as well as having a wide insecticidal spectrum. One of the target pests for this protein is the fall armyworm (FAW) (Spodoptera frugiperda), the most important corn pest in South America. Previously it has been controlled by insecticides and corn expressing Cry proteins, but has rapidly evolved resistance to many control practices and remains a top concern for sustainable biotechnology control efforts. Thus, resistance characterization involving mode of action and genetics of resistance can help with Insect Resistance Management strategies, and improve the durability of control. In this dissertation, using selected FAW population resistant to Vip3Aa20 Bt protein (Vip-R1and Vip-R2) we generated comparative proteomic and transcriptomic data among resistant and susceptible colonies. In the chapter 2, we bring FAW biology/ecology and Brazilian agriculture landscape data to support the high adaptive potential of this pest to genetically modified corn expressing Bt Cry proteins in Brazil. -
Cross-Crop Resistance of Spodoptera Frugiperda Selected on Bt Maize To
www.nature.com/scientificreports OPEN Cross‑crop resistance of Spodoptera frugiperda selected on Bt maize to genetically‑modifed soybean expressing Cry1Ac and Cry1F proteins in Brazil Eduardo P. Machado1, Gerson L. dos S. Rodrigues Junior1, Fábio M. Führ1, Stefan L. Zago1, Luiz H. Marques2*, Antonio C. Santos2, Timothy Nowatzki3, Mark L. Dahmer3, Celso Omoto4 & Oderlei Bernardi1* Spodoptera frugiperda is one of the main pests of maize and cotton in Brazil and has increased its occurrence on soybean. Field‑evolved resistance of this species to Cry1 Bacillus thuringiensis (Bt) proteins expressed in maize has been characterized in Brazil, Argentina, Puerto Rico and southeastern U.S. Here, we conducted studies to evaluate the survival and development of S. frugiperda strains that are susceptible, selected for resistance to Bt‑maize single (Cry1F) or pyramided (Cry1F/Cry1A.105/ Cry2Ab2) events and F 1 hybrids of the selected and susceptible strains (heterozygotes) on DAS‑ 444Ø6‑6 × DAS‑81419‑2 soybean with tolerance to 2,4‑d, glyphosate and ammonium glufosinate herbicides (event DAS‑444Ø6‑6) and insect‑resistant due to expression of Cry1Ac and Cry1F Bt proteins (event DAS‑81419‑2). Susceptible insects of S. frugiperda did not survive on Cry1Ac/Cry1F‑ soybean. However, homozygous‑resistant and heterozygous insects were able to survive and emerge as fertile adults when fed on Cry1Ac/Cry1F‑soybean, suggesting that the resistance is partially recessive. Life history studies revealed that homozygous‑resistant insects had similar development, reproductive performance, net reproductive rate, intrinsic and fnite rates of population increase on Cry1Ac/Cry1F‑soybean and non‑Bt soybean. In contrast, heterozygotes had their fertility life table parameters signifcantly reduced on Cry1Ac/Cry1F‑soybean. -
Striped Earwig
Beneficial Species Profile Photo credit: Joseph Berger, Bugwood.org Common Name: Striped Earwig Scientific Name: Labidura riparia Order and Family: Dermaptera: Labiduridae Size and Appearance: A small, mostly soft-bodied insect that appears pale brown in color with two lengthwise stripes on the pronotum, which is the protective outer plate covering the insect’s thorax. Front wings appear to be shortened and disguise much longer hind wings folded up beneath. Large pincher-like cerci, which are paired appendages at the end of the abdomen. Male cerci are widely separated at the base, slightly curved, and symmetrical. Antenna have 14-24 segments; 4th, 5th & 6th antennae segments combined are shorter than the 1st segment. 2nd tarsal segment is cylindrical, not lobed. Length (mm) Appearance Egg ~ 1mm but can swell to over Pearly grayish-white; laid in clustered double the size while uptaking masses water during development Larva/Nymph Strongly resemble the adult without 2mm- 18mm developed wings; whitish appearance when first born; 4 instars Adult Pale brown in color; front wings appear to be shortened and disguise much 18-26mm longer hind wings folded up beneath; Large pincher-like cerci on abdomen; antennae have 14-24 segments; 4th, 5th & 6th antennae segments combined are shorter than the 1st segment. 2nd tarsal segment is cylindrical, not lobed. Pupa (if applicable) Incomplete Metamorphosis (no pupae) n/a Type of feeder (Chewing, sucking, etc.): Chewing mouthparts on adult and immature. Host/s: Widespread and found on a variety of hosts in all life cycles including, but not limited to, ground litter, beaches, river banks, and irrigation fields. -
Insect Pest Management in Soybeans 12 by G
Chapter Insect Pest Management in Soybeans 12 by G. Lorenz, D. Johnson, G. Studebaker, C. Allen and S. Young, III he importance of insect pests in Arkansas Finally, it is important to determine what soybeans is extremely variable from year to management tactics are available and whether or year due in large part to environmental not they are economically feasible. T conditions. For example, hot, dry years favor many lepidopterous pests such as the soybean Insect Identification podworm and the beet armyworm; and when drought conditions occur, these pests usually are The three types of insect pests found in soybeans abundant. Many other lepidopterous pests, such as in Arkansas are: the velvetbean caterpillar and the soybean looper, 1. Foliage feeders, which comprise the biggest may cause problems following migrations from group of insect pests, southern areas, particularly in concurrence with winds out of the Gulf region where they are a 2. Pod feeders, which are probably the most common problem. Generally, insect pressure is detrimental to yield, and greater in the southern part of the state compared to 3. Stem, root and seedling feeders, which are northern Arkansas due to warmer temperatures and often the hardest to sample and are not detected closeness to the aforementioned migration sources. until after they have caused damage. Production practices also have an impact on the Some insects, such as the bean leaf beetle, may feed GEMENT occurrence of pest insects in soybeans. For example, on both foliage and pods but are primarily insects such as the Dectes stem borer and grape considered foliage feeders. -
Natural Distribution of Parasitoids of Larvae of the Fall Armyworm, <I
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 2009 Natural distribution of parasitoids of larvae of the fall armyworm, Spodoptera frugiperda, in Argentina M Gabriela Murua Estación Experimental Agroindustrial Obispo Colombres, CONICET Jamie Molina Ochoa Universidad de Colima, University of Nebraska-Lincoln Patricio Fidalgo CRILAR Follow this and additional works at: http://digitalcommons.unl.edu/entomologyfacpub Part of the Entomology Commons Murua, M Gabriela; Ochoa, Jamie Molina; and Fidalgo, Patricio, "Natural distribution of parasitoids of larvae of the fall armyworm, Spodoptera frugiperda, in Argentina" (2009). Faculty Publications: Department of Entomology. 384. http://digitalcommons.unl.edu/entomologyfacpub/384 This Article is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications: Department of Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Journal of Insect Science: Vol. 9 | Article 20 Murúa et al. Natural distribution of parasitoids of larvae of the fall armyworm, Spodoptera frugiperda, in Argentina M. Gabriela Murúaa,b, Jaime Molina-Ochoac,d and Patricio Fidalgoe aEstación Experimental Agroindustrial Obispo Colombres, Sección Zoología Agrícola, CC 9, Las Talitas (T4101XAC), Tucumán, Argentina bCONICET cUniversidad de Colima, Facultad de Ciencias Biológicas y Agropecuarias, Km. 40, autopista Colima-Manzanillo, Tecomán, Colima (28100), México dDepartment of Entomology, University of Nebraska-Lincoln, Lincoln, NE 68583-0816, USA eCRILAR (CONICET), entre Ríos y Mendoza s/n, Anillaco (5301), La Rioja, Argentina Abstract To develop a better understanding of the natural distribution of the fall armyworm, Spodoptera frugiperda (Smith) (Lepidoptera: Noctuidae), and to update the knowledge of the incidence of its complex of parasitoids. -
Abundance and Diversity of Ground-Dwelling Arthropods of Pest Management Importance in Commercial Bt and Non-Bt Cotton Fields
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by DigitalCommons@University of Nebraska University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 2007 Abundance and diversity of ground-dwelling arthropods of pest management importance in commercial Bt and non-Bt cotton fields J. B. Torres Universidade Federal Rural de Pernarnbuco, [email protected] J. R. Ruberson University of Georgia Follow this and additional works at: https://digitalcommons.unl.edu/entomologyfacpub Part of the Entomology Commons Torres, J. B. and Ruberson, J. R., "Abundance and diversity of ground-dwelling arthropods of pest management importance in commercial Bt and non-Bt cotton fields" (2007). Faculty Publications: Department of Entomology. 762. https://digitalcommons.unl.edu/entomologyfacpub/762 This Article is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications: Department of Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Annals of Applied Biology ISSN 0003-4746 RESEARCH ARTICLE Abundance and diversity of ground-dwelling arthropods of pest management importance in commercial Bt and non-Bt cotton fields J.B. Torres1,2 & J.R. Ruberson2 1 Departmento de Agronomia – Entomologia, Universidade Federal Rural de Pernambuco, Dois Irma˜ os, Recife, Pernambuco, Brazil 2 Department of Entomology, University of Georgia, Tifton, GA, USA Keywords Abstract Carabidae; Cicindelinae; Falconia gracilis; genetically modified cotton; Labiduridae; The modified population dynamics of pests targeted by the Cry1Ac toxin in predatory heteropterans; Staphylinidae. -
A Synergism Between Dimethyl Trisulfide and Methyl Thiolacetate
University of Connecticut OpenCommons@UConn Department of Ecology and Evolutionary EEB Articles Biology 2020 A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically-Supplemented Minimal Trap Stephen T. Trumbo University of Connecticut at Waterbury, [email protected] John Dicapua III University of Connecticut at Waterbury, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/eeb_articles Part of the Behavior and Ethology Commons, and the Entomology Commons Recommended Citation Trumbo, Stephen T. and Dicapua, John III, "A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically- Supplemented Minimal Trap" (2020). EEB Articles. 46. https://opencommons.uconn.edu/eeb_articles/46 1 1 2 A Synergism Between Dimethyl Trisulfide And Methyl Thiolacetate In Attracting 3 Carrion-Frequenting Beetles Demonstrated By Use Of A Chemically-Supplemented 4 Minimal Trap 5 6 Stephen T. Trumbo* and John A. Dicapua III 7 8 University of Connecticut, Department of Ecology and Evolutionary Biology, 9 Waterbury, Connecticut, USA 10 11 *Department of Ecology and Evolutionary Biology, University of Connecticut, 99 E. 12 Main St., Waterbury, CT 06710, U.S.A. ([email protected]) 13 ORCID - 0000-0002-4455-4211 14 15 Acknowledgements 16 We thank Alfred Newton (staphylinids), Armin MocZek and Anna Macagno (scarabs) 17 for their assistance with insect identification. Sandra Steiger kindly reviewed the 18 manuscript. The Southern Connecticut Regional Water Authority and the Flanders 19 Preserve granted permission for field experiments. The research was supported by 20 the University of Connecticut Research Foundation. -
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 -
U.S. EPA, Pesticide Product Label, LAMBDA 13% INSECTICIDE, 04/24
EPA Reg. Number: Date of Issuance: US. ENVIRONMENTAI.PR<lTECTION AGENCY 71532-20 Office of Pesticide Programs APR 2 4 20D7 Registration Division (H7505C) 1200 Pl:nnsylvania Avenue, N.W. Washington, D.c' 20460 NOTICE OF PESTICIDE: L Registration _ Reregistration (Under FrFRA as amended) Name LG Life Sciences, Ltd. c/o Biologic Inc. 115 Obtuse Hill Road and Rodenticide Act. Registration is in no way to bc construed as an endorsement or recommendation of this product by the Agency. In order to prot~t health and the : environment, the Administrator, on his motion, may at any time suspend or cancel the registratIOn of a pesticide in accordance with the Act. The acceptance , of any name in conneCtion with the registration of a product under this Act is not to be construed as giving the registrant a right to exclusive use of the name or to its use if it has been covered by others. This product is conditionally registercd in accordance with PIFRA sec. 3(c)(7)(A), subject to the following provisions: 1. You will submit andlor cite all data required for registration/reregistration of your pmduct under FIFRA sec. 3( c)(5) when the Agency requires all registrants of similar products to submit su;h data; and submit acceptable responses required for reregistration of your product under FIFRA sectior 4. 2. You will make the following label changes before you release the product for shipmmt: a) Revise the EPA Registration Number to read "EPA Reg. No.71532-20." b) Add "Contains petroleum distillates" immediately below the ingredient statement as a footnote below the term "Inert ingredients." c) Under First Aid list the statcments in the following order: "If on skin or clothing, Ifin eyes, If swallowed, If inhaled." d) Revise the 2"d bullet of the "If Swallowed" first aid statements to read "Do not give any liquid to the person." e) Add H(PPE)" after the Personal Protective Equipment headi!lg on page 3. -
The Fall Armyworm – a Pest of Pasture and Hay
The Fall Armyworm – A Pest of Pasture and Hay. Allen Knutson Extension Entomologist, Texas A&M AgriLife Extension Texas A&M AgriLife Research and Extension Center, Dallas, 2019 revision The fall armyworm, Spodoptera frugiperda, is a common pest of bermudagrass, sorghum, corn, wheat and rye grass and many other crops in north and central Texas. Larvae of fall armyworms are green, brown or black with white to yellowish lines running from head to tail. A distinct white line between the eyes forms an inverted “Y” pattern on the face. Four black spots aligned in a square on the top of the segment near the back end of the caterpillar are also characteristic. Armyworms are very small (less than 1/8 inch) at first, cause little plant damage and as a result often go unnoticed. Larvae feed for 2-3 weeks and full grown larvae are about 1 to 1 1/2 inches long. Given their immense appetite, great numbers, and marching ability, fall armyworms can damage entire fields or pastures in a few days. Once the armyworm larva completes feeding, it tunnels into the soil to a depth of about an inch and enters the pupal stage. The armyworm moth emerges from the pupa in about ten days and repeats the life cycle. The fall armyworm moth has a wingspan of about 1 1/2 inches. The front pair of wings is dark gray with an irregular pattern of light and dark areas. Moths are active at night when they feed on nectar and deposit egg masses. A single female can deposit up to 2000 eggs and there are four to five generations per year.