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Da Flyer General
The Citrus Root Weevil The citrus root weevil, Diaprepes abbreviatus, is a large colorful weevil that is native to the Caribbean Islands. This weevil was accidentally introduced into Florida in the 1960’s where it has caused extensive damage. It has been intercepted in shipments of plants to California. This weevil will feed on about 270 different plants including citrus, guava, loquat, holly, and other ornamentals. An adult citrus root weevil (approximate size a to w inch in length). 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 12345678901234567890123456789012123456789012345678901234567890121234567890123456789012345678901212345678901234567890123456789012123456789012345678901234 -
Integration of Entomopathogenic Fungi Into IPM Programs: Studies Involving Weevils (Coleoptera: Curculionoidea) Affecting Horticultural Crops
insects Review Integration of Entomopathogenic Fungi into IPM Programs: Studies Involving Weevils (Coleoptera: Curculionoidea) Affecting Horticultural Crops Kim Khuy Khun 1,2,* , Bree A. L. Wilson 2, Mark M. Stevens 3,4, Ruth K. Huwer 5 and Gavin J. Ash 2 1 Faculty of Agronomy, Royal University of Agriculture, P.O. Box 2696, Dangkor District, Phnom Penh, Cambodia 2 Centre for Crop Health, Institute for Life Sciences and the Environment, University of Southern Queensland, Toowoomba, Queensland 4350, Australia; [email protected] (B.A.L.W.); [email protected] (G.J.A.) 3 NSW Department of Primary Industries, Yanco Agricultural Institute, Yanco, New South Wales 2703, Australia; [email protected] 4 Graham Centre for Agricultural Innovation (NSW Department of Primary Industries and Charles Sturt University), Wagga Wagga, New South Wales 2650, Australia 5 NSW Department of Primary Industries, Wollongbar Primary Industries Institute, Wollongbar, New South Wales 2477, Australia; [email protected] * Correspondence: [email protected] or [email protected]; Tel.: +61-46-9731208 Received: 7 September 2020; Accepted: 21 September 2020; Published: 25 September 2020 Simple Summary: Horticultural crops are vulnerable to attack by many different weevil species. Fungal entomopathogens provide an attractive alternative to synthetic insecticides for weevil control because they pose a lesser risk to human health and the environment. This review summarises the available data on the performance of these entomopathogens when used against weevils in horticultural crops. We integrate these data with information on weevil biology, grouping species based on how their developmental stages utilise habitats in or on their hostplants, or in the soil. -
Diaspididae (Hemiptera: Coccoidea) En Olivo, <I>Olea Europaea</I>
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 2014 Diaspididae (Hemiptera: Coccoidea) en olivo, Olea europaea Linnaeus (Oleaceae), en Brasil Vera Regina dos Santos Wolff Fundação Estadual de Pesquisa Agropecuária (FEPAGRO), [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi dos Santos Wolff, Vera Regina, "Diaspididae (Hemiptera: Coccoidea) en olivo, Olea europaea Linnaeus (Oleaceae), en Brasil" (2014). Insecta Mundi. 900. http://digitalcommons.unl.edu/insectamundi/900 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI A Journal of World Insect Systematics 0385 Diaspididae (Hemiptera: Coccoidea) en olivo, Olea europaea Linnaeus (Oleaceae), en Brasil Vera Regina dos Santos Wolff Fundação Estadual de Pesquisa Agropecuária (FEPAGRO) Rua Gonçalves Dias 570. Porto Alegre Rio Grande do Sul, Brasil Date of Issue: September 26, 2014 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Vera Regina dos Santos Wolff Diaspididae (Hemiptera: Coccoidea) en olivo, Olea europaea Linnaeus (Oleaceae), en Brasil Insecta Mundi 0385: 1–6 ZooBank Registered: urn:lsid:zoobank.org:pub:8ED57F9D-E002-4269-88DA-A8DBDB41F57E Published in 2014 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod. Topics considered for publication include systematics, taxonomy, nomenclature, checklists, faunal works, and natural history. -
Arthropod Pests of Citrus Roots
lds. r at ex ual to ap ila red t is een vi Clayton W. McCoy fa University of Florida ks Citrus Res ea rch and Educati on Center, Lake Alfred )0 Ily I'::y les Ill up 10 Arthropod Pests of Citrus Roots 'ul r-J!l 'Ie '](1 cc The major arthropods that are injurious to plant roots are Geographical Distribution members of the classes Insecta and Acari (mites). Two-thi rds of these pests are members of the order Coleoptera (beetles), Citrus root weevi ls are predominantly trop ical ; however, a which as larvae cause serious economic loss in a wide range few temperate species are important pests in the United States, of plan t hosts. Generally, the larvae hatch from eggs laid by Chile. Argentina. Australia. and New Zealand (Table 14.1). adults on plan ts or in the soil and complete part of their life The northern blue-green citrus root weevil, Pachnaeus opalus; cycle chewing on plant roots, and in many cases as adults the Fuller rose beetle, Asynonychus godmani: and related spe they feed on the foli age of the same or other host plan ts. A cies in the genus Pantomorus are found in temperate areas. Ap number of arthropods inhabit the rhizosphere of citrus trees. proximately 150 species have been recorded in the Caribbean some as unique syrnbionts, but few arc injurious to the roots. region, including Florida. Central America, and South America, Only citrus root weevils. termi tes. and ants. in descending or feeding as larvae on the roots of all species of the genus Citrus. -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
Parasitism of the Soybean Aphid, Aphis Glycines by Binodoxys Communis: the Role of Aphid Defensive Behaviour and Parasitoid Reproductive Performance
Bulletin of Entomological Research (2008) 98, 361–370 doi:10.1017/S000748530800566X Ó 2008 Cambridge University Press Printed in the United Kingdom First published online 25 February 2008 Parasitism of the soybean aphid, Aphis glycines by Binodoxys communis: the role of aphid defensive behaviour and parasitoid reproductive performance K.A.G. Wyckhuys1 *, L. Stone3, N. Desneux2, K.A. Hoelmer4, K.R. Hopper4 and G.E. Heimpel2 1Horticulture Research Center, Universidad Jorge Tadeo Lozano, Chia (Cundinamarca), Colombia: 2Department of Entomology, University of Minnesota, St. Paul, USA: 3Saint Olaf College, Northfield, Minnesota, USA: 4Beneficial Insect Introductions Research Unit, USDA-ARS, Newark, Delaware, USA Abstract The Asian parasitoid, Binodoxys communis (Gahan) (Hymenoptera: Braconidae), is a candidate for release against the exotic soybean aphid, Aphis glycines Matsumura (Hemiptera: Aphididae), in North America. In this study, we examined preferences by B. communis for the different developmental stages of A. glycines and investigated consequences of these preferences for parasitoid fitness. We also determined to what extent aphid defensive behaviours mediate such preferences. We found that B. communis readily attacks and successfully develops in the different A. glycines developmental stages. Binodoxys communis development time gradually increased with aphid developmental stage, and wasps took longest to develop in alates. An average (+SE) of 54.01+0.08% of parasitized A. glycines alatoid nymphs transformed into winged adult aphids prior to mummification. No-choice assays showed a higher proportion of successful attacks for immature apterous A. glycines nymphs compared to adults and alatoid nymphs. Also, choice trials indicated avoidance and lower attack and oviposition of adults and alatoid nymphs. -
Diversity of Buprestidae (Coleoptera) from El Limón De Cuauchichinola, Tepalcingo, Morelos, Mexico Author(S): Angélica M
Diversity of Buprestidae (Coleoptera) from El Limón de Cuauchichinola, Tepalcingo, Morelos, Mexico Author(s): Angélica M. Corona-López, Emma V. Reza-Pérez, Víctor H. Toledo- Hernández, Alejandro Flores-Palacios, Ted C. Macrae, Richard L. Westcott, Henry A. Hespenheide and Charles L. Bellamy Source: Pan-Pacific Entomologist, 93(2):71-83. Published By: Pacific Coast Entomological Society https://doi.org/10.3956/2017-93.2.71 URL: http://www.bioone.org/doi/full/10.3956/2017-93.2.71 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/ terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. THE PAN-PACIFIC ENTOMOLOGIST 93(2):71–83, (2017) Diversity of Buprestidae (Coleoptera) from El Limón de Cuauchichinola, Tepalcingo, Morelos, Mexico 1, 1 ANGÉLICA M. CORONA-LÓPEZ *, EMMA V. REZA-PÉREZ , 1 1 VÍCTOR H. TOLEDO-HERNÁNDEZ , ALEJANDRO FLORES-PALACIOS , 2 3 4 TED C. MACRAE , RICHARD L. WESTCOTT , HENRY A. -
International Symposium on Biological Control of Arthropods 424 Poster Presentations ______
POSTER PRESENTATIONS ______________________________________________________________ Poster Presentations 423 IMPROVEMENT OF RELEASE METHOD FOR APHIDOLETES APHIDIMYZA (DIPTERA: CECIDOMYIIDAE) BASED ON ECOLOGICAL AND BEHAVIORAL STUDIES Junichiro Abe and Junichi Yukawa Entomological Laboratory, Kyushu University, Japan ABSTRACT. In many countries, Aphidoletes aphidimyza (Rondani) has been used effectively as a biological control agent against aphids, particularly in greenhouses. In Japan, A. aphidimyza was reg- istered as a biological control agent in April 1999, and mass-produced cocoons have been imported from The Netherlands and United Kingdom since mass-rearing methods have not yet been estab- lished. In recent years, the effect of imported A. aphidimyza on aphid populations was evaluated in greenhouses at some Agricultural Experiment Stations in Japan. However, no striking effect has been reported yet from Japan. The failure of its use in Japan seems to be caused chiefly by the lack of detailed ecological or behavioral information of A. aphidimyza. Therefore, we investigated its ecological and behavioral attributes as follows: (1) the survival of pupae in relation to the depth of pupation sites; (2) the time of adult emergence in response to photoperiod during the pupal stage; (3) the importance of a hanging substrate for successful mating; and (4) the influence of adult size and nutrient status on adult longev- ity and fecundity. (1) A commercial natural enemy importer in Japan suggests that users divide cocoons into groups and put each group into a plastic container filled with vermiculite to a depth of 100 mm. However, we believe this is too deep for A. aphidimyza pupae, since under natural conditions mature larvae spin their cocoons in the top few millimeters to a maxmum depth of 30 mm. -
Aphid-Parasitoid (Insecta) Diversity and Trophic Interactions in South Dakota
Proceedings of the South Dakota Academy of Science, Vol. 97 (2018) 83 APHID-PARASITOID (INSECTA) DIVERSITY AND TROPHIC INTERACTIONS IN SOUTH DAKOTA Abigail P. Martens* and Paul J. Johnson Insect Biodiversity Lab South Dakota State University Brookings, SD 57007 *Corresponding author email: [email protected] ABSTRACT Parasitoid wasps of the subfamily Aphidiinae (Hymenoptera: Braconidae) specialize on aphids (Hemiptera: Aphididae) as hosts. The diversity of known and probable aphidiine wasps from South Dakota is itemized, with represen- tation by 13 genera and 42 species, 43% of which are probably adventitious. The wasps and aphids are central to various combinations of multitrophic relationships involving host plants and secondary parasitoids. Selected native and introduced aphid host taxa were quantitatively and qualitatively collected from diverse native and crop host plants in eastern South Dakota and western Iowa. Wasps were reared to confirm plant association, host aphid association, taxonomic diversity, and native or introduced status of the wasps. Acanthocaudus tissoti (Smith) and Aphidius (Aphidius) ohioensis (Smith) were found together on the native aphid Uroleucon (Uroleucon) nigrotuberculatum (Olive), a new host aphid species for both wasps on Solidago canadensis L. (Asterales: Asteraceae). The native waspLysiphlebus testaceipes (Cresson) was repeatedly reared in mas- sive numbers from mummies of invasive Aphis glycines Matsumura on soybean, Glycine max (L.) Merr. This wasp was also reared from the non-nativeAphis nerii Boyer de Fonscolombe and the native Aphis asclepiadis Fitch, both on Asclepias syriaca L. The introduced wasp Binodoxys communis (Gahan) was not recovered from any Aphis glycines population. Hyperparasitoids from the genus Dendrocerus Ratzeburg (Hymenoptera: Megaspilidae), and the pteromalid (Hymenoptera: Pteromalidae) genera Asaphes Walker, and Pachyneuron Walker were reared from mummies of Uroleucon (Uroleucon) nigrotuberculatum parasitized by either Acanthocaudus tissoti or Aphidius (Aphidius) ohioensis. -
Use of Landscape Fabric to Manage Diaprepes Root Weevil in Citrus Groves
Use of Landscape Fabric to Manage Diaprepes Root Weevil in Citrus Groves Authors: L. W. Duncan, R. J. Stuart, F. G. Gmitter, and S. L. Lapointe Source: Florida Entomologist, 92(1) : 74-79 Published By: Florida Entomological Society URL: https://doi.org/10.1653/024.092.0112 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/Florida-Entomologist on 21 Jun 2019 Terms of Use: https://bioone.org/terms-of-use 74 Florida Entomologist 92(1) March 2009 USE OF LANDSCAPE FABRIC TO MANAGE DIAPREPES ROOT WEEVIL IN CITRUS GROVES L. W. DUNCAN,1 R. J. STUART1, F. G. GMITTER2 AND S. L. LAPOINTE3 1Department of Entomology and Nematology and 2Department of Horticultural Sciences, University of Florida, IFAS, Citrus Research and Education Center, 700 Experiment Station Road, Lake Alfred, FL 33850 3U. S. Horticultural Research Lab, U. -
Aspidiotus Nerii Bouchè (Insecta: Hemipthera: Diaspididae)
University of Massachusetts Amherst ScholarWorks@UMass Amherst Masters Theses 1911 - February 2014 2003 Molecular systematics of a sexual and parthenogenetic species complex : Aspidiotus nerii Bouchè (Insecta: Hemipthera: Diaspididae). Lisa M. Provencher University of Massachusetts Amherst Follow this and additional works at: https://scholarworks.umass.edu/theses Provencher, Lisa M., "Molecular systematics of a sexual and parthenogenetic species complex : Aspidiotus nerii Bouchè (Insecta: Hemipthera: Diaspididae)." (2003). Masters Theses 1911 - February 2014. 3090. Retrieved from https://scholarworks.umass.edu/theses/3090 This thesis is brought to you for free and open access by ScholarWorks@UMass Amherst. It has been accepted for inclusion in Masters Theses 1911 - February 2014 by an authorized administrator of ScholarWorks@UMass Amherst. For more information, please contact [email protected]. MOLECULAR SYSTEMATICS OF A SEXUAL AND PARTHENOGENETIC SPECIES COMPLEX: Aspidiotus nerii BOUCHE (INSECTA: HEMIPTERA: DIASPIDIDAE). A Thesis Presented by LISA M. PROVENCHER Submitted to the Graduate School of the University of Massachusetts Amherst in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE May 2003 Entomology MOLECULAR SYSTEMATICS OF A SEXUAL AND PARTHENOGENETIC SPECIES COMPLEX: Aspidiotus nerii BOUCHE (INSECTA: HEMIPTERA: DIASPIDIDAE). A Thesis Presented by Lisa M. Provencher Roy G. V^n Driesche, Department Head Department of Entomology What is the opposite of A. nerii? iuvf y :j3MSuy ACKNOWLEDGEMENTS I thank Edward and Mari, for their patience and understanding while I worked on this master’s thesis. And a thank you also goes to Michael Sacco for the A. nerii jokes. I would like to thank my advisor Benjamin Normark, and a special thank you to committee member Jason Cryan for all his generous guidance, assistance and time. -
A Contribution to the Aphid Fauna of Greece
Bulletin of Insectology 60 (1): 31-38, 2007 ISSN 1721-8861 A contribution to the aphid fauna of Greece 1,5 2 1,6 3 John A. TSITSIPIS , Nikos I. KATIS , John T. MARGARITOPOULOS , Dionyssios P. LYKOURESSIS , 4 1,7 1 3 Apostolos D. AVGELIS , Ioanna GARGALIANOU , Kostas D. ZARPAS , Dionyssios Ch. PERDIKIS , 2 Aristides PAPAPANAYOTOU 1Laboratory of Entomology and Agricultural Zoology, Department of Agriculture Crop Production and Rural Environment, University of Thessaly, Nea Ionia, Magnesia, Greece 2Laboratory of Plant Pathology, Department of Agriculture, Aristotle University of Thessaloniki, Greece 3Laboratory of Agricultural Zoology and Entomology, Agricultural University of Athens, Greece 4Plant Virology Laboratory, Plant Protection Institute of Heraklion, National Agricultural Research Foundation (N.AG.RE.F.), Heraklion, Crete, Greece 5Present address: Amfikleia, Fthiotida, Greece 6Present address: Institute of Technology and Management of Agricultural Ecosystems, Center for Research and Technology, Technology Park of Thessaly, Volos, Magnesia, Greece 7Present address: Department of Biology-Biotechnology, University of Thessaly, Larissa, Greece Abstract In the present study a list of the aphid species recorded in Greece is provided. The list includes records before 1992, which have been published in previous papers, as well as data from an almost ten-year survey using Rothamsted suction traps and Moericke traps. The recorded aphidofauna consisted of 301 species. The family Aphididae is represented by 13 subfamilies and 120 genera (300 species), while only one genus (1 species) belongs to Phylloxeridae. The aphid fauna is dominated by the subfamily Aphidi- nae (57.1 and 68.4 % of the total number of genera and species, respectively), especially the tribe Macrosiphini, and to a lesser extent the subfamily Eriosomatinae (12.6 and 8.3 % of the total number of genera and species, respectively).