Vegetable Insects Indentification
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Epidemiology and Disease Management of Stewart's Disease of Corn in Iowa Paul David Esker Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 2005 Epidemiology and disease management of Stewart's disease of corn in Iowa Paul David Esker Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Agriculture Commons, and the Plant Pathology Commons Recommended Citation Esker, Paul David, "Epidemiology and disease management of Stewart's disease of corn in Iowa " (2005). Retrospective Theses and Dissertations. 1727. https://lib.dr.iastate.edu/rtd/1727 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Epidemiology and disease management of Stewart's disease of corn in Iowa by Paul David Esker A dissertation submitted to the graduate faculty in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Co-majors: Plant Pathology; Statistics Program of Study Committee: Philip M. Dixon, Co-major Professor Forrest W. Nutter, Jr., Co-major Professor Charles C. Block Petrutza C. Caragea Mark L. Gleason S. Elwynn Taylor Iowa State University Ames, Iowa 2005 UMI Number: 3200414 INFORMATION TO USERS The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleed-through, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. -
Insect Management
C H A P T E R 5 INSECT MANAGEMENT “change in form.” Pests of field crops undergo either sim- LEARNING OBJECTIVES ple or complete metamorphosis. After completely studying this chapter, you should: Group 1. Simple Metamorphosis I Understand how insects grow and develop. When insects that develop by simple metamorphosis hatch from their eggs, they resemble the adult insects I Understand the difference between simple and com- except that the immatures, or nymphs, do not have plete metamorphosis. wings. Nymphs periodically molt, growing larger. After I Be able to identify general and major insect pests of the final molt, nymphs become adults and generally have alfalfa, corn, dry beans, soybeans, small grains, and wings. Many pests of field crops such as potato leafhop- sugar beets. per, sugarbeet root aphid, tarnished plant bug, and grasshoppers develop by simple metamorphosis. I Be able to describe the life cycles and habitats of the Nymphs and adults are often found together in the crop major field crop pests. and usually eat the same food. Insect damage reduces crop yield or quality, or conta- minates the final product. Insects can also transmit plant diseases. To effectively control insect pests, you should understand how insects grow and develop. Egg Nymphs Adult GROWTH AND DEVELOPMENT A plant bug is an example of an insect with simple Growth metamorphosis. An insect’s body is confined in a protective exoskele- Group 2. Complete Metamorphosis ton. This hard outer covering does not grow continuous- ly. A new, soft exoskeleton is formed under the old one, Insects that develop by complete metamorphosis and the old exoskeleton is shed—a process called molt- make a radical change in appearance from immature to ing. -
BD5208 Wide Scale Enhancement of Biodiversity (WEB) Final Report on Phase 2, and Overview of Whole Project Executive Summary
BD5208 Wide Scale Enhancement of Biodiversity (WEB) Final report on phase 2, and overview of whole project Executive summary Core objective The WEB project aimed to inform the development of new or existing Entry Level (ELS) and Higher Level Stewardship scheme (HLS) options that create grassland of modest biodiversity value, and deliver environmental ecosystem services, on large areas of land with little or no potential for creation or restoration of BAP Priority Habitat grassland. Specific objectives Quantify the success of establishing a limited number of plant species into seedbeds (ELS/HLS creation option) and existing grassland (currently HLS restoration option) to provide pollen, nectar, seed, and/or spatial and structural heterogeneity. Quantify the effects of grassland creation and sward restoration on faunal diversity/abundance, forage production and quality, soil properties and nutrient losses. Develop grazing and cutting management practices to enhance biodiversity, minimise pollution and benefit agronomic performance. Liaise with Natural England to produce specifications for new or modified ES options, and detailed guidance for their successful management. Overview of experiment: The vast majority of lowland grasslands in the UK have been agriculturally improved, receiving inputs of inorganic fertiliser, reseeding, improved drainage and are managed with intensive cutting and grazing regimes. While this has increased livestock productivity it has led to grasslands that are species-poor in both native plants and invertebrates. To rectify this simple Entry Level Stewardship scheme options have been developed that reduce fertiliser inputs; this includes the EK2 and EK3 options. While permanent grasslands receiving low fertiliser inputs account for the largest area of lowland managed under the agri-environment schemes they currently provide only minimal benefits for biodiversity or ecosystem services. -
Chrysomela 43.10-8-04
CHRYSOMELA newsletter Dedicated to information about the Chrysomelidae Report No. 43.2 July 2004 INSIDE THIS ISSUE Fabreries in Fabreland 2- Editor’s Page St. Leon, France 2- In Memoriam—RP 3- In Memoriam—JAW 5- Remembering John Wilcox Statue of 6- Defensive Strategies of two J. H. Fabre Cassidine Larvae. in the garden 7- New Zealand Chrysomelidae of the Fabre 9- Collecting in Sholas Forests Museum, St. 10- Fun With Flea Beetle Feces Leons, France 11- Whither South African Cassidinae Research? 12- Indian Cassidinae Revisited 14- Neochlamisus—Cryptic Speciation? 16- In Memoriam—JGE 16- 17- Fabreries in Fabreland 18- The Duckett Update 18- Chrysomelidists at ESA: 2003 & 2004 Meetings 19- Recent Chrysomelid Literature 21- Email Address List 23- ICE—Phytophaga Symposium 23- Chrysomela Questionnaire See Story page 17 Research Activities and Interests Johan Stenberg (Umeå Univer- Duane McKenna (Harvard Univer- Eduard Petitpierre (Palma de sity, Sweden) Currently working on sity, USA) Currently studying phyloge- Mallorca, Spain) Interested in the cy- coevolutionary interactions between ny, ecological specialization, population togenetics, cytotaxonomy and chromo- the monophagous leaf beetles, Altica structure, and speciation in the genus somal evolution of Palearctic leaf beetles engstroemi and Galerucella tenella, and Cephaloleia. Needs Arescini and especially of chrysomelines. Would like their common host plant Filipendula Cephaloleini in ethanol, especially from to borrow or exchange specimens from ulmaria (meadow sweet) in a Swedish N. Central America and S. America. Western Palearctic areas. Archipelago. Amanda Evans (Harvard University, Maria Lourdes Chamorro-Lacayo Stefano Zoia (Milan, Italy) Inter- USA) Currently working on a phylogeny (University of Minnesota, USA) Cur- ested in Old World Eumolpinae and of Leptinotarsa to study host use evolu- rently a graduate student working on Mediterranean Chrysomelidae (except tion. -
Corn Flea Beetle
Pest Profile Photo credit: North Central Branch-Entomological Society of America, UNL-Entomology Extension Common Name: Corn flea beetle Scientific Name: Chaetocnema pulicaria Order and Family: Coleoptera, Chrysomelidae Size and Appearance: Length (mm) Appearance white have a pointy end Egg ~0.35 darken slightly in color before hatching white slimly shaped Larva/Nymph < 9 cylindrical prothorax and last abdominal segment are slightly darkened small shiny black Adult < 2 enlarged hind legs white Pupa (if soft in texture applicable) gets dark before development is complete Type of feeder (Chewing, sucking, etc.): Chewing mouthparts Host plant/s: Corn is the preferred host plant, but they are also found on a number of different grass types, oats, Timothy, barley and wheat. Description of Damage (larvae and adults): The adult corn flea beetle injures corn plants by removing leaf tissue and by transmitting pathogenic bacteria. Injury by the adults appears as scratches in the upper and lower surfaces of the leaf, usually parallel to the veins. They feed on both the upper and the lower epidermis of corn leaves, but they do not chew completely through the leaves. The scratches rarely result in economy injury. The leaves of severely injured plants appear whitish or silvery. More importantly, the beetles transmit the bacterium Erwinia stewartia, the casual organism of Stewart’s wilt, to susceptible varieties of corn. Field corn infested with Stewart’s disease will show little sign of disease until late in the summer when numerous leaf lesions will appear on the leaves. The result is often small ears or no ears at all. -
CERTAIN INSECT VECTORS of APLANOBACTER STEWARTI ' by F
CERTAIN INSECT VECTORS OF APLANOBACTER STEWARTI ' By F. W. Poos, senior entomologist, Division of Cereal and Forage Insects, Bureau of Entomology and Plant Quarantine; and CHARLOTTE ELLIOTT, associate pa- thologist, Division of Cereal Crops and Diseases, Bureau of Plant Industry, United States Department of Agriculture ^ INTRODUCTION Bacterial wilt of corn (Zea mays L.) caused by Aplanobacter stewarti (E. F. Sm.) McC. was exceedingly destructive and more widely dis- tributed during 1932 and 1933 than during any previous time in the history of the disease. Since 1897, when it was first described by Stewart, it has been studied by a number of investigators whose work has pointed more and more toward insects as a means of dis- semination of the causal organism. Kand and Cash (7) ^ during 1920-23 found that bacterial wilt could be transmitted from diseased to healthy com plants by two species of flea beetles, Chaetocnema pulicaria Melsh. and C, denticulata (111.), and by the spotted cucum- ber beetle, Diabrotica duodecimpunctata (Fab.). IvanoíF (ö) reported transmission from diseased to healthy plants by the larval stage of the corn rootworm, Diabrotica longicornis (Say), as it attacked the roots of young seedling com plants. He also reported that the bac- teria of A. stewarti entered the corn plants through wounds made by white grubs, the larvae of Phyllophaga sp., feeding upon the roots in infested soil. A summary of this work, together with a brief review of the other literature on this disease, has recently appeared else- where (1), The results of experiments by previous investigators on soil trans- mission of the causal organism indicate that transmission through the soil to uninjured roots of com plants is exceedingly rare, if it ever occurs. -
Insects for Weed Control: Status in North Dakota
Insects for Weed Control: Status in North Dakota E. U. Balsbaugh, Jr. Associate Professor, Department of Entomology R. D. Frye Professor, Department of Entomology C. G. Scholl Plant Protection Specialist, North Dakota State Department of Agriculture A. W. Anderson Associate Professor, Department of Entomology Two foreign species of weevils have been introduced into North Dakota for the biological control of musk thistle, Carduus nutans L. - Rhinocyllus conicus (Froelich), a seed feeding weevH, and Ceutorrhynchidius horridus (Panzer), an internal root and lower stem inhabiting species. R. conicus has survived for several generations and is showing some promise for thistle suppression in Walsh County, but releases of C. hor ridus have been unsuccessful. The pigweed nea beetle, Disonycha glabrata (Fab.), which is native in southern United States, has been introduced into experimental sugarbeet plots in the Red River Valley for testing its effects at controlling rough pigweed or redroot, Amaranthus retroflexus L. Although both larvae and adults of these beetles feed heavily on pigweed, damage to the weed occurs too late in the season for them to be effective in suppressing weed growth or seed set. An initial survey for native insects of bindweed has been conducted. Feeding by localized populations of various insects, particularly tortoise beetles, has been observed. Several foreign species of nea beetles and a stem boring beetle are anticipated for release against leafy spurge. Entomologists at North Dakota State University are successful. In 1940, the cactus-feeding moth, Cac studying insects that feed on weeds to determine if the toblastis cactorum (Berg), was transported from its insects can reduce populations of selected weeds to native Argentina to Australia where it greatly reduced levels at which the weeds no longer are economically im the numbers of prickly pear cactus, Opuntia spp. -
Article-P605.Pdf
J. AMER. SOC. HORT. SCI. 118(5):605-608. 1993. Potential of Non-chemical Control Strategies for Reduction of Soil Insect Damage in Sweetpotato J.M. Schalk1, J.R. Bohac2, and P.D. Dukes3 U.S. Department of Agriculture, Agricultural Research Service, U.S. Vegetable Laboratory, 2875 Savannah Highway, Charleston, SC 29414 W.R. Martin4 Biosys, 1057 East Meadow Circle, Palo Alto, CA 94303 Additional index words. Ipomoea batatas, parasitic nematode, plant resistance, biological control, wireworms, flea beetles, grubs, cucumber beetles Abstract. This 2-year study was conducted to determine if soil insect damage could be reduced in sweetpotato [Ipomoea batatas (L.) Lam] by treatment with an insecticide (fonofos) and/or a parasitic nematode (Steinernema carpocapsae Weiser), in conjunction with sweetpotato cultivars that differed in susceptibility to soil insect damage. Analysis of field data for the first year showed that the parasitic nematode provided significant damage protection of sweetpotato from wireworms (Conoderus spp.), Diabrotica sp., Systena sp., and sweetpotato flea beetle (Chaetocnema confinis Crotch), but not from grubs (Plectris aliena Chapin; Phyllophaga ephilida Say). In this same test, fonofos used alone provided protection against wireworm- Diabrotica-Systena (WDS complex) damage. In the second test, the nematode did not provide soil insect protection for the WDS complex, but fonofos did reduce damage for these insects. Poor efficacy in the second test with the nematode probably was due to high rainfall, which saturated the soil. Resistant cultivars provided good protection for all three categories of damage. When used with the insect-susceptible check ‘SC 1149-19’, the nematode or fonofos treatments provided better control for all insect categories in the first test. -
PIGWEED FLEA BEETLE (Disonycha Glabrata) (Coleoptera: Chrysomelidae)
Rose Hiskes, Diagnostician and Horticulturist Department of Entomology The Connecticut Agricultural Experiment Station 123 Huntington Street, P. O. Box 1106 New Haven, CT 06504 Phone: (203) 974-8600 Fax: (203) 974-8502 Founded in 1875 Email: [email protected] Putting science to work for society Website: www.ct.gov/caes PIGWEED FLEA BEETLE (Disonycha glabrata) (Coleoptera: Chrysomelidae) Pigweeds are serious agricultural weeds in the This native beetle is found from California to Amaranth family. This would lead one to Florida in the Southern United States. In the believe a pigweed flea beetle would be a great Northern United States it is found from New biological control organism. However, there York to the foothills of the Rockies. are species of amaranth used for food, both as a grain and a leafy vegetable, and as In the Caribbean it is found on the islands of ornamentals (e.g., Love-Lies-Bleeding). In Jamaica and Trinidad. It is also found in Jamaica, callaloo refers to Amaranthus Central and South America. viridis, a pigweed that is harvested prior to flowering and mainly used as a steamed green vegetable. If left to flower, the grain produced is high in lysine and when combined with other grains, provides good human nutrition. The pigweed flea beetle is becoming a problem for callaloo producers in Connecticut. Figure 2. Damage to callaloo caused by the pigweed flea beetle. Photo by Richard Cowles. DAMAGE Adults feed on foliage, chewing small, round holes (Fig. 2). Larvae are also foliage feeders. Heavy feeding results in early leaf drop and Figure 1. -
Redheaded Flea Beetle Integrated Pest Management Andrew Kness and Brian A
Redheaded Flea Beetle Integrated Pest Management Andrew Kness and Brian A. Kunkel, University of Delaware, Department of Entomology & Wildlife Ecology, Newark, DE ABSTRACT: Redheaded flea beetle (Systena frontalis) has become a serious pest insect of woody and herbaceous ornamental plants over the last several years. Our research focused on identifying when key life stages of the redheaded flea beetle were active and correlating these stages with growing degree day (GDD) data and plant phonological indicators (PPIs). Choice and no-choice feeding assays were conducted to determine host plant preferences. Entomopathogenic nematodes (epns) were applied to containers in field experiments at two locations to evaluate efficacy against the soil-dwelling larvae. Overwintering eggs hatch with larvae active between 257– 481 GDD50, and the corresponding PPIs were black locust and Chinese fringetree in full bloom. First adult emergence occurred between 590– 785 GDD50, and the PPIs were Magnolia grandiflora in flower bud swell to bloom. The second generation of larvae was found between 1818– 1860 GDD50 and the following plants were in the indicated phenological stage: 1) Hosta in full bloom, 2) Crape Myrtle ‘Hopi Pink’ bloom to full bloom, 3) Crape Myrtle ‘Siren Red’ flower bud swell, 4) Hibisucs in bloom and 5) Cerastigma plumbaginoides in bloom. Field observations and choice tests found S. frontalis feeds on many different hosts and exhibited little preference between host plants tested. Field trials with epns did not provide significant control of S. frontalis larvae in either experiment. Further work with potting media, soil temperatures and irrigation needs to continue in order to improve EPN efficacy. -
Biology of Diamondback Moth, Plutellae Xylostella (Lepidoptera: Plutellidae) of Cauliflower Under Laboratory Condition
Int.J.Curr.Microbiol.App.Sci (2019) 8(1): 866-873 International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Volume 8 Number 01 (2019) Journal homepage: http://www.ijcmas.com Original Research Article https://doi.org/10.20546/ijcmas.2019.801.094 Biology of Diamondback Moth, Plutellae xylostella (Lepidoptera: Plutellidae) of Cauliflower under Laboratory Condition G. Harika1*, S. Dhurua2, N. Sreesandhya2, M. Suresh2 and S. Govinda Rao2 1DAATTC, Vizianagaram, AP, India 2ANGRAU, Agricultural College, Naira, A.P, India *Corresponding author ABSTRACT K e yw or ds Biological studies conducted during 2017-18 at the Post Graduation Research laboratory, Department of Entomology, Agricultural College, Naira on Diamondback moth, Plutellae Biology, Plutellae xylostella (L.) (Lepidoptera: Plutellidae) revealed that the egg period (incubation period) xylostella , varies from 2 to 4 days (Av. 3 ± 0.5 days). The larva passed through four different instars. Cauliflower The first, second, third and fourth instar larva lived for 2 to 3 days (Av. 2.5 days), 2 days (Av. 1.5 days), 1 to 3 days (Av. 1.75 ± 0.25 days) and 2 to 4 days (Av. 2.75 ± 0.25 days), Article Info respectively with a total larval period of 7 to 12 days (Av. 9 days). The pre-pupal and Accepted: pupal stage lasted for 1 - 2 days (Av. 1.5 ± 0.5 days) and 3 to 5 days (Av. 4.25 ± 0.25 07 December 2018 days), respectively. The adults lived for 3 to 7 days (Av. 4.5 ± 1 days) and the entire life Available Online: span under laboratory conditions varied from 13 to 22 days (Av. -
Diversity and Abundance of Pest Insects Associated with Solanum Tuberosum L
American Journal of Entomology 2021; 5(3): 51-69 http://www.sciencepublishinggroup.com/j/aje doi: 10.11648/j.aje.20210503.13 ISSN: 2640-0529 (Print); ISSN: 2640-0537 (Online) Diversity and Abundance of Pest Insects Associated with Solanum tuberosum L. 1753 (Solanaceae) in Balessing (West-Cameroon) Babell Ngamaleu-Siewe, Boris Fouelifack-Nintidem, Jeanne Agrippine Yetchom-Fondjo, Basile Moumite Mohamed, Junior Tsekane Sedick, Edith Laure Kenne, Biawa-Miric Kagmegni, * Patrick Steve Tuekam Kowa, Romaine Magloire Fantio, Abdel Kayoum Yomon, Martin Kenne Department of the Biology and Physiology of Animal Organisms, University of Douala, Douala, Cameroon Email address: *Corresponding author To cite this article: Babell Ngamaleu-Siewe, Boris Fouelifack-Nintidem, Jeanne Agrippine Yetchom-Fondjo, Basile Moumite Mohamed, Junior Tsekane Sedick, Edith Laure Kenne, Biawa-Miric Kagmegni, Patrick Steve Tuekam Kowa, Romaine Magloire Fantio, Abdel Kayoum Yomon, Martin Kenne. Diversity and Abundance of Pest Insects Associated with Solanum tuberosum L. 1753 (Solanaceae) in Balessing (West-Cameroon). American Journal of Entomology . Vol. 5, No. 3, 2021, pp. 51-69. doi: 10.11648/j.aje.20210503.13 Received : July 14, 2021; Accepted : August 3, 2021; Published : August 11, 2021 Abstract: Solanum tuberosum L. 1753 (Solanaceae) is widely cultivated for its therapeutic and nutritional qualities. In Cameroon, the production is insufficient to meet the demand in the cities and there is no published data on the diversity of associated pest insects. Ecological surveys were conducted from July to September 2020 in 16 plots of five development stages in Balessing (West- Cameroon). Insects active on the plants were captured and identified and the community structure was characterized.