Biological Control of Mole Crickets
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The Digger Wasps of Saudi Arabia: New Records and Distribution, with a Checklist of Species (Hym.: Ampulicidae, Crabronidae and Sphecidae)
NORTH-WESTERN JOURNAL OF ZOOLOGY 9 (2): 345-364 ©NwjZ, Oradea, Romania, 2013 Article No.: 131206 http://biozoojournals.3x.ro/nwjz/index.html The digger wasps of Saudi Arabia: New records and distribution, with a checklist of species (Hym.: Ampulicidae, Crabronidae and Sphecidae) Neveen S. GADALLAH1,*, Hathal M. AL DHAFER2, Yousif N. ALDRYHIM2, Hassan H. FADL2 and Ali A. ELGHARBAWY2 1. Entomology Department, Faculty of Science, Cairo University, Giza, Egypt. 2. Plant Protection Department, College of Food and Agriculture Science, King Saud University, King Saud Museum of Arthropod (KSMA), Riyadh, Saudi Arabia. *Corresponing author, N.S. Gadalah, E-mail: [email protected] Received: 24. September 2012 / Accepted: 13. January 2013 / Available online: 02. June 2013 / Printed: December 2013 Abstract. The “sphecid’ fauna of Saudi Arabia (Hymenoptera: Apoidea) is listed. A total of 207 species in 42 genera are recorded including previous and new species records. Most Saudi Arabian species recorded up to now are more or less common and widespread mainly in the Afrotropical and Palaearctic zoogeographical zones, the exception being Bembix buettikeri Guichard, Bembix hofufensis Guichard, Bembix saudi Guichard, Cerceris constricta Guichard, Oxybelus lanceolatus Gerstaecker, Palarus arabicus Pulawski in Pulawski & Prentice, Tachytes arabicus Guichard and Tachytes fidelis Pulawski, which are presumed endemic to Saudi Arabia (3.9% of the total number of species). General distribution and ecozones, and Saudi Arabian localities are given for each species. In this study two genera (Diodontus Curtis and Dryudella Spinola) and 11 species are newly recorded from Saudi Arabia. Key words: Ampulicidae, Crabronidae, Sphecidae, faunistic list, new records, Saudi Arabia. Introduction tata boops (Schrank), Bembecinus meridionalis A.Costa, Diodontus sp. -
Incorporating Genomics Into the Toolkit of Nematology
Journal of Nematology 44(2):191–205. 2012. Ó The Society of Nematologists 2012. Incorporating Genomics into the Toolkit of Nematology 1 2 1,* ADLER R. DILLMAN, ALI MORTAZAVI, PAUL W. STERNBERG Abstract: The study of nematode genomes over the last three decades has relied heavily on the model organism Caenorhabditis elegans, which remains the best-assembled and annotated metazoan genome. This is now changing as a rapidly expanding number of nematodes of medical and economic importance have been sequenced in recent years. The advent of sequencing technologies to achieve the equivalent of the $1000 human genome promises that every nematode genome of interest will eventually be sequenced at a reasonable cost. As the sequencing of species spanning the nematode phylum becomes a routine part of characterizing nematodes, the comparative approach and the increasing use of ecological context will help us to further understand the evolution and functional specializations of any given species by comparing its genome to that of other closely and more distantly related nematodes. We review the current state of nematode genomics and discuss some of the highlights that these genomes have revealed and the trend and benefits of ecological genomics, emphasizing the potential for new genomes and the exciting opportunities this provides for nematological studies. Key words: ecological genomics, evolution, genomics, nematodes, phylogenetics, proteomics, sequencing. Nematoda is one of the most expansive phyla docu- piece of knowledge we can currently obtain for any mented with free-living and parasitic species found in particular life form (Consortium, 1998). nearly every ecological niche(Yeates, 2004). Traditionally, As in many other fields of biology, the nematode C. -
Diptera: Tachinidae) Larvae
Welch: Competition by Ormia depleta 497 INTRASPECIFIC COMPETITION FOR RESOURCES BY ORMIA DEPLETA (DIPTERA: TACHINIDAE) LARVAE C. H. WELCH USDA/ARS/cmave, 1600 SW 23rd Drive, Gainesville, FL 32608 ABSTRACT Ormia depleta is a parasitoid of pest mole crickets in the southeastern United States. From 2 to 8 larvae of O. depleta were placed on each of 368 mole cricket hosts and allowed to de- velop. The weights of the host crickets, number of larvae placed, number of resulting pupae, and the weights of those pupae were all factored to determine optimal parasitoid density per host under laboratory rearing conditions. Based on larval survival and pupal weight, this study indicates that 4-5 larvae per host is optimal for laboratory rearing. Key Words: biocontrol, Scapteriscus, parasitoid, superparasitism RESUMEN Ormia depleta es un parasitoide de grillotopos en el sureste de los Estados Unidos. Entre 2 y 8 larvas de O. depleta se colocaron en 368 grillotopos huéspedes y se dejaron madurar. El peso de los huéspedes, el número de larvas de O. depleta colocadas, el número de pupas re- sultantes y el peso de las pupas fueron usados para determinar la densidad optima de para- sitoides en cada huésped para ser usadas en la reproducción de este parasitoide en el laboratorio. Nuestros resultados muestran que entre 4 y 5 larvas por cada grillotopo es la densidad optima para la reproducción en el laboratorio de este parasitoide. Translation provided by the author. Ormia depleta (Wiedemann) is a parasitoid of protocol requires hand inoculation of 3 planidia Scapteriscus spp. mole crickets, imported pests of under the posterior margin of the pronotum of turf and pasture grasses in the southeastern each host (R. -
A Review of Sampling and Monitoring Methods for Beneficial Arthropods
insects Review A Review of Sampling and Monitoring Methods for Beneficial Arthropods in Agroecosystems Kenneth W. McCravy Department of Biological Sciences, Western Illinois University, 1 University Circle, Macomb, IL 61455, USA; [email protected]; Tel.: +1-309-298-2160 Received: 12 September 2018; Accepted: 19 November 2018; Published: 23 November 2018 Abstract: Beneficial arthropods provide many important ecosystem services. In agroecosystems, pollination and control of crop pests provide benefits worth billions of dollars annually. Effective sampling and monitoring of these beneficial arthropods is essential for ensuring their short- and long-term viability and effectiveness. There are numerous methods available for sampling beneficial arthropods in a variety of habitats, and these methods can vary in efficiency and effectiveness. In this paper I review active and passive sampling methods for non-Apis bees and arthropod natural enemies of agricultural pests, including methods for sampling flying insects, arthropods on vegetation and in soil and litter environments, and estimation of predation and parasitism rates. Sample sizes, lethal sampling, and the potential usefulness of bycatch are also discussed. Keywords: sampling methodology; bee monitoring; beneficial arthropods; natural enemy monitoring; vane traps; Malaise traps; bowl traps; pitfall traps; insect netting; epigeic arthropod sampling 1. Introduction To sustainably use the Earth’s resources for our benefit, it is essential that we understand the ecology of human-altered systems and the organisms that inhabit them. Agroecosystems include agricultural activities plus living and nonliving components that interact with these activities in a variety of ways. Beneficial arthropods, such as pollinators of crops and natural enemies of arthropod pests and weeds, play important roles in the economic and ecological success of agroecosystems. -
Mole Crickets Scapteriscus Spp
Mole Crickets Scapteriscus spp. Southern mole cricket, Scapteriscus borellii Tawny mole cricket, Scapteriscus vicinus DESCRIPTION OF INSECT All stages live in the soil and are rarely see on the surface. Immature stage Nymphs of both species are similar in appearance to adults, but lack wings. Nymphs proceed through 8-10 instars ranging in size from 0.2 to 1.25 inches in length. Each instar is progressively larger with wing buds apparent on later instars. Color varies from gray to brown. Pronotum (large shield behind head) with distinctive mottling or spots, depending on species and location. Mature stage Adults are somewhat cylindrically shaped, light colored crickets 1.26 to 1.38 inches in length. Adults have two pairs of wings, but only fly at night during two brief flight periods in fall and early spring. Spring flights are generally more extensive than fall flights. Damaging stage(s) Both nymphs and adults cause damage Predictive models (degree day, plant phenology, threat temperatures, other) Eggs being to hatch at threat temperatures of 65° F and higher (spring/early summer in most locations). Egg-laying and hatch timing are affected by soil moisture. Threat temperatures can be used to trigger preventive treatments. See the article, “Threat temperatures” for more information. Preventive treatments should be applied prior to egg-hatch (early June) or at the time of peak hatch (last week of June, first week of July in most years and locations). Weekly soap flushes in June and early July is the best method to determine when hatch is occurring, and the best time to treat. -
Long-Term Mole Cricket Control on Horizon
Long-term mole cricket control on horizon A nematode product patented for use by the University of Florida to provide long-term biological con- trol of turf-damaging mole crickets will be available next year from Becker Underwood. This product, known as Nematac S, will be cost-effective and highly beneficial for a wide range of consumers, from golf- course managers to ranchers. By Angela Brammer UF graduate student The parasitic nematode Stein- ernema scapterisci attacks only for- eign mole crickets — those that are most damaging to turfgrasses in the Southeast. The nematodes live in the soil and enter the mole cricket through openings in the body, such as the mouth or spiracles. Once in- side, they release bacteria that feed on the mole cricket, usually killing it within 48 hours. The nematodes feed on the bacteria and reproduce inside the mole cricket, and the next generation emerges to search for another host once it dies. Steinernema scapterisci spreads slowly on its own, mostly relying on University of Florida/Dr. K.B. Nguyen its host for dispersal. After infection, Steinernema scapterisci nematodes emerge from the body of a dead a mole cricket may fly up to a mile, tawny mole cricket. taking its parasitic nematodes along for the ride. Nematodes then emerge on insecticides to prevent such dam- Applying them just beneath the sur- into the new location once the host age. face provides some protection from cricket dies. Because of this, it may In the 1980s, University of Flor- desiccation and ultraviolet light. be possible to effectively cover an ida scientists imported the mole Surface distribution should be fol- area of mole cricket infestation by cricket nematode from South Amer- lowed by irrigation to help the applying the nematodes to the “hot ica. -
Tawny Mole Cricket
INSECT PESTS Tawny Mole Cricket Prepared by Camille Goodwin, MG 2008 Texas AgriLife Extension Service Galveston County Office Dickinson, TX 77539 Educational programs of the Texas AgriLife Extension Service are open to all people without regard to race, color, sex, disability, religion, age, or national origin. The Texas A&M System, U.S. Department of Agriculture and the County Commissioners Courts of Texas cooperating. FIG. 1 Type Pest: chewing insect (Scapteriscus vicinus Scudder) • Another closely related mole cricket, the southern mole cricket (Scapteriscus borellia Giglio-Tos) also occurs in the Galveston-Houston area Type Metamorphous: simple (egg, nymph and adult stages) Period of Primary Activity: April through October Plants Affected • Bermudagrass and bahiagrass are the primary turfgrasses damaged by the mole cricket, although extensive damage can be sustained on cultivars of St. Augustinegrass, FIG. 2 centipedegrass, ryegrass, zoysiagrass and bentgrass • Tomato, strawberry, beet, cabbage, cantaloupe, carrot, cauliflower, collard, eggplant, kale, lettuce, onion, pepper, potato, spinach, sweet potato, turnip, flowers such as coleus, chrysanthemum, gypsophila, and other plants • Mole crickets feed on other soil-dwelling insects Identifying Characteristics of Insect Pest EGG STAGE • After mating and dispersal flights occur, females lay eggs in cells dug in the soil primarly during April with some egg laying occurring into early summer • Eggs hatch in about 2 weeks FIG. 3 NYMPH STAGES • Nymphs develop through eight juvenile stages (separated by molts) mostly during the summer months. • Each successive growth stage (instar) is larger and looks more and more like the adult but lack fully developed wings • Winter is spent as partially grown nymphs and as adults ADULT STAGE (Fig. -
Mole Cricket: Scapteriscus Vicinus Shortwinged Mole Cricket: Scapteriscus Abbreviatus
Tawny Mole Cricket: Scapteriscus vicinus Shortwinged Mole Cricket: Scapteriscus abbreviatus Biology & Lifecycle: Adults and larger nymphs chew on stems of seedlings and smaller plants at the soil surface. The tawny mole cricket has one generation each year and overwinters as adults, which lay eggs in April through early June. Nymphs grow slowly through the summer months and start becoming adults in September. The shortwinged mole cricket is almost restricted to coastal areas. Most eggs are laid in late spring through early summer. Females of both species lay clutches of eggs in underground egg chambers. Environmental Factors: Tawny and shortwinged mole crickets are present year-around, with adults and large nymphs overwintering but inactivated by cold temperatures and drought (they burrow deeper underground). Irrigation during drought allows them to be active. Flooding forces them to migrate to higher ground. Adult: Adults are large, about 1¼ inches, with wings longer than body (tawny mole cricket (Figure 3)) or very much shorter than body (shortwinged mole cricket (Figure 1)). Both adults and nymphs have enlarged and toothed forelegs for digging; expanded femurs (base of the hind legs) for jumping, although only nymphs jump. All species have soft bodies, with the middle body section protected by a hardened cover (pronotum). Immature: Nymphs range from less than 1/8 inch at hatching to about 1 inch several months later, resembling the adults but without trace of wings in the first 4 instars and with small wing buds in later instars. The number of molts varies from 6 to 9 (Figure 5). Host range: Both species attack seedlings of eggplant, sweet pepper, tobacco, tomato and cabbage. -
Olfaction Shapes Host–Parasite Interactions in Parasitic Nematodes
Olfaction shapes host–parasite interactions in PNAS PLUS parasitic nematodes Adler R. Dillmana, Manon L. Guillerminb, Joon Ha Leeb, Brian Kima, Paul W. Sternberga,1, and Elissa A. Hallemb,1 aHoward Hughes Medical Institute, Division of Biology, California Institute of Technology, Pasadena, CA 91125; and bDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095 Contributed by Paul W. Sternberg, July 9, 2012 (sent for review May 8, 2012) Many parasitic nematodes actively seek out hosts in which to host recognition (19). IJs then infect the host either by entering complete their lifecycles. Olfaction is thought to play an important through natural orifices or by penetrating through the insect role in the host-seeking process, with parasites following a chem- cuticle (20). Following infection, IJs release a bacterial endo- ical trail toward host-associated odors. However, little is known symbiont into the insect host and resume development (21–23). about the olfactory cues that attract parasitic nematodes to hosts The bacteria proliferate inside the insect, producing an arsenal or the behavioral responses these cues elicit. Moreover, what little of secondary metabolites that lead to rapid insect death and is known focuses on easily obtainable laboratory hosts rather digestion of insect tissues. The nematodes feed on the multi- than on natural or other ecologically relevant hosts. Here we in- plying bacteria and the liberated nutrients of broken-down in- vestigate the olfactory responses of six diverse species of ento- sect tissues. They reproduce in the cadaver until resources are mopathogenic nematodes (EPNs) to seven ecologically relevant depleted, at which time new IJs form and disperse in search of potential invertebrate hosts, including one known natural host new hosts (24). -
Nematodes As Biocontrol Agents This Page Intentionally Left Blank Nematodes As Biocontrol Agents
Nematodes as Biocontrol Agents This page intentionally left blank Nematodes as Biocontrol Agents Edited by Parwinder S. Grewal Department of Entomology Ohio State University, Wooster, Ohio USA Ralf-Udo Ehlers Department of Biotechnology and Biological Control Institute for Phytopathology Christian-Albrechts-University Kiel, Raisdorf Germany David I. Shapiro-Ilan United States Department of Agriculture Agriculture Research Service Southeastern Fruit and Tree Nut Research Laboratory, Byron, Georgia USA CABI Publishing CABI Publishing is a division of CAB International CABI Publishing CABI Publishing CAB International 875 Massachusetts Avenue Wallingford 7th Floor Oxfordshire OX10 8DE Cambridge, MA 02139 UK USA Tel: þ44 (0)1491 832111 Tel: þ1 617 395 4056 Fax: þ44 (0)1491 833508 Fax: þ1 617 354 6875 E-mail: [email protected] E-mail: [email protected] Web site: www.cabi-publishing.org ßCAB International 2005. All rights reserved. No part of this publication may be reproduced in any form or by any means, electronically, mech- anically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Nematodes as biocontrol agents / edited by Parwinder S. Grewal, Ralf- Udo Ehlers, David I. Shapiro-Ilan. p. cm. Includes bibliographical references and index. ISBN 0-85199-017-7 (alk. paper) 1. Nematoda as biological pest control agents. I. Grewal, Parwinder S. II. Ehlers, Ralf-Udo. III. Shaprio-Ilan, David I. SB976.N46N46 2005 632’.96–dc22 2004030022 ISBN 0 85199 0177 Typeset by SPI Publisher Services, Pondicherry, India Printed and bound in the UK by Biddles Ltd., King’s Lynn This volume is dedicated to Dr Harry K. -
Howard Frank Professor Emeritus
J. Howard Frank Professor Emeritus Contact: PO Box 110620 Building 970, Natural Area Dr. Gainesville, FL 32611 (352) 273-3922 [email protected] Education B.Sc. (Honors), Durham University, England (Zoology), 1963 D.Phil., Oxford University, England (Entomology), 1967 Relevant Employment History Professor (1987-2012) Entomology and Nematology Department, University of Florida Associate Professor (1985-1987) Entomology and Nematology Department, University of Florida Associate Professor (1983-1985) Florida Medical Entomology Lab, Vero Beach, FL Entomologist (1972-1983) Entomological Research Center (later Florida Medical Entomology Lab), Vero Beach, FL Entomologist (1968-1972) Research Department, Sugar Manufacturers' Association, Mandeville, Jamaica Post-doctoral Fellow (1966-1968) Entomology Department, University of Alberta, Canada Former Research Responsibilities Biological control of pest insects using parasitoids, predators, or pathogens. Current projects are against Scapteriscus mole crickets (pests of turf, pasture grasses, and vegetables), and Metamasius callizona (pest of bromeliads). Former Teaching responsibilities Biological Control (ENY 5241), a course for graduate students. Tropical Entomology for undergraduates (ENY 3563/ENY 3564L) and for graduates (ENY 5566/ENY 5567L). Supervision of research by graduate students. Former Extension responsibilities Extension of results of the research project Accomplishments Introduction, colonization, release, and establishment in at least 38 Florida counties of Ormia depleta (Diptera: Tachinidae) -
Caribbean Food Crops Society Serving the Caribbean Since 1963 Caribbean Food Crops Society 40
CARIBBEAN FOOD CROPS SOCIETY SERVING THE CARIBBEAN SINCE 1963 CARIBBEAN FOOD CROPS SOCIETY 40 Fortieth Annual Meeting 2004 Proceedings of the Caribbean Food Crops Society. 40:249-183. 2004 A COMMERCI AL NEMATODE FOR MOLE CRICKET CONTROL N.C. Leppla1, J.H. Frank', N. Vicente2 and A. Pantoja3. 1 University of Florida, IF AS, P.O. Box 110620, Gainesville, FL 32611-0620, 2University of Puerto Rico, Agricultural Experiment Station, P.O. Box 9030, Mayaguez, PR 00681-9030, United States Department of Agriculture, ARS, SARU, Fairbanks, AK99775-7200 ABSTRACT: In Puerto Rico, the name "changa" is generally applied to Scapteriscus didactylus (Latreille) (Orthoptera: Gryllotalpidae), the most widespread and damaging of the non- indigenous pest mole crickets in Puerto Rico. S. abbreviatus Scudder is also established but much less abundant. We conducted a T-STAR project to efficiently release, establish, distribute and evaluate the entomopathogenic nematode, Stinernema scapterisci Nguyen and Smart (Rhabditida: Steinernematidae), for controlling Scapteriscus spp. mole crickets. The University of Florida negotiated an agreement with Becker Underwood for commercial production of the nematode that is available as the product, Nematac®S. The "mole cricket nematode" has been used effectively to control non-indigenous mole crickets in pastures and turf in Florida since the early 1990s. It parasitizes only Scapteriscus spp. in nature and not indigenous mole crickets that are in a different genus, so it is safe to import and release. The level of mole cricket infection, nematode establishment and dispersal, and suppression of mole cricket populations is being quantified. This project provided data on the occurrence and life history of Scapteriscus spp.