Illustration of the Morphologic Characters of the Sunn Pest
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Zootaxa,Phylogeny and Higher Classification of the Scale Insects
Zootaxa 1668: 413–425 (2007) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2007 · Magnolia Press ISSN 1175-5334 (online edition) Phylogeny and higher classification of the scale insects (Hemiptera: Sternorrhyncha: Coccoidea)* P.J. GULLAN1 AND L.G. COOK2 1Department of Entomology, University of California, One Shields Avenue, Davis, CA 95616, U.S.A. E-mail: [email protected] 2School of Integrative Biology, The University of Queensland, Brisbane, Queensland 4072, Australia. Email: [email protected] *In: Zhang, Z.-Q. & Shear, W.A. (Eds) (2007) Linnaeus Tercentenary: Progress in Invertebrate Taxonomy. Zootaxa, 1668, 1–766. Table of contents Abstract . .413 Introduction . .413 A review of archaeococcoid classification and relationships . 416 A review of neococcoid classification and relationships . .420 Future directions . .421 Acknowledgements . .422 References . .422 Abstract The superfamily Coccoidea contains nearly 8000 species of plant-feeding hemipterans comprising up to 32 families divided traditionally into two informal groups, the archaeococcoids and the neococcoids. The neococcoids form a mono- phyletic group supported by both morphological and genetic data. In contrast, the monophyly of the archaeococcoids is uncertain and the higher level ranks within it have been controversial, particularly since the late Professor Jan Koteja introduced his multi-family classification for scale insects in 1974. Recent phylogenetic studies using molecular and morphological data support the recognition of up to 15 extant families of archaeococcoids, including 11 families for the former Margarodidae sensu lato, vindicating Koteja’s views. Archaeococcoids are represented better in the fossil record than neococcoids, and have an adequate record through the Tertiary and Cretaceous but almost no putative coccoid fos- sils are known from earlier. -
Heteroptera: Coreidae: Coreinae: Leptoscelini)
Brailovsky: A Revision of the Genus Amblyomia 475 A REVISION OF THE GENUS AMBLYOMIA STÅL (HETEROPTERA: COREIDAE: COREINAE: LEPTOSCELINI) HARRY BRAILOVSKY Instituto de Biología, UNAM, Departamento de Zoología, Apdo Postal 70153 México 04510 D.F. México ABSTRACT The genus Amblyomia Stål is revised and two new species, A. foreroi and A. prome- ceops from Colombia, are described. New host plant and distributional records of A. bifasciata Stål are given; habitus illustrations and drawings of male and female gen- italia are included as well as a key to the known species. The group feeds on bromeli- ads. Key Words: Insecta, Heteroptera, Coreidae, Leptoscelini, Amblyomia, Bromeliaceae RESUMEN El género Amblyomia Stål es revisado y dos nuevas especies, A. foreroi y A. prome- ceops, recolectadas en Colombia, son descritas. Plantas hospederas y nuevas local- idades para A. bifasciata Stål son incluidas; se ofrece una clave para la separación de las especies conocidas, las cuales son ilustradas incluyendo los genitales de ambos sexos. Las preferencias tróficas del grupo están orientadas hacia bromelias. Palabras clave: Insecta, Heteroptera, Coreidae, Leptoscelini, Amblyomia, Bromeli- aceae The neotropical genus Amblyomia Stål was previously known from a single Mexi- can species, A. bifasciata Stål 1870. In the present paper the genus is redefined to in- clude two new species collected in Colombia. This genus apparently is restricted to feeding on members of the Bromeliaceae, and specimens were collected on the heart of Ananas comosus and Aechmea bracteata. -
2010 Central Asia IPM
Annual Report FY 2009-10 Oct0ber 1, 2009 to September 30, 2010 Development and Delivery of Ecologically-based IPM Packages in Central Asia Project Management: Dr. Karim Maredia (PI), Michigan State University Dr. Zakir Khalikulov, CGIAR/ICARDA-Project Facilitation Unit, Tashkent, Uzbekistan Wheat IPM Package: Dr. Nurali Saidov, IPM CRSP Coordinator, Tajikistan Dr. Doug Landis, Michigan State University Dr. Bohssini Mustapha, ICARDA Dr. Megan Kennelly, Kansas State University Tomato IPM Package: Dr. Barno Tashpulatova, IPM CRSP Coordinator, Uzbekistan Dr. Frank Zalom, University of California-Davis Dr. Ravza Mavlyanova, AVRDC/World Vegetable Center Potato IPM Package: Dr. Murat Aitmatov, IPM CRSP Coordinator, Kyrgyzstan Dr. David Douches, Michigan State University Dr. George Bird, Michigan State University Dr. Walter Pett, Michigan State University IPM Communication: Ms. Joy Landis, Michigan State University Links with IPM CRSP Global Theme Projects: Pest Diagnostics: Dr. Sally Miller, Ohio State University Viruses: Dr. Naidu Rayapati, Washington State University and Dr. Sue Tolin, Virginia Tech University Gender Issues: Dr. Linda Racioppi and Dr. Zahra Jamal, Michigan State University and Dr. Maria Elisa Christie, Virginia Tech University Socio-Economic Impact Assessment: Dr. Mywish Maredia and Richard Bernsten, Michigan State University, and Dr. George Norton, Virginia Tech University 1 Michigan State University (MSU) in partnership with University of California-Davis, Kansas State University, ICARDA, AVRDC, and several local research and academic institutions and NGOs is implementing a regional IPM program in Central Asia. The three host countries include - Tajikistan, Uzbekistan and Kyrgyzstan. The technical objectives of the Central Asia Regional IPM Program are as follow: 1. Develop ecologically based IPM packages for wheat, tomato and potato through collaborative research and access to new technologies. -
Correlation of Stylet Activities by the Glassy-Winged Sharpshooter, Homalodisca Coagulata (Say), with Electrical Penetration Graph (EPG) Waveforms
ARTICLE IN PRESS Journal of Insect Physiology 52 (2006) 327–337 www.elsevier.com/locate/jinsphys Correlation of stylet activities by the glassy-winged sharpshooter, Homalodisca coagulata (Say), with electrical penetration graph (EPG) waveforms P. Houston Joosta, Elaine A. Backusb,Ã, David Morganc, Fengming Yand aDepartment of Entomology, University of Riverside, Riverside, CA 92521, USA bUSDA-ARS Crop Diseases, Pests and Genetics Research Unit, San Joaquin Valley Agricultural Sciences Center, 9611 South Riverbend Ave, Parlier, CA 93648, USA cCalifornia Department of Food and Agriculture, Mt. Rubidoux Field Station, 4500 Glenwood Dr., Bldg. E, Riverside, CA 92501, USA dCollege of Life Sciences, Peking Univerisity, Beijing, China Received 5 May 2005; received in revised form 29 November 2005; accepted 29 November 2005 Abstract Glassy-winged sharpshooter, Homalodisca coagulata (Say), is an efficient vector of Xylella fastidiosa (Xf), the causal bacterium of Pierce’s disease, and leaf scorch in almond and oleander. Acquisition and inoculation of Xf occur sometime during the process of stylet penetration into the plant. That process is most rigorously studied via electrical penetration graph (EPG) monitoring of insect feeding. This study provides part of the crucial biological meanings that define the waveforms of each new insect species recorded by EPG. By synchronizing AC EPG waveforms with high-magnification video of H. coagulata stylet penetration in artifical diet, we correlated stylet activities with three previously described EPG pathway waveforms, A1, B1 and B2, as well as one ingestion waveform, C. Waveform A1 occured at the beginning of stylet penetration. This waveform was correlated with salivary sheath trunk formation, repetitive stylet movements involving retraction of both maxillary stylets and one mandibular stylet, extension of the stylet fascicle, and the fluttering-like movements of the maxillary stylet tips. -
Eurygaster Integriceps Put.)
FAT BODY ROLE IN THE DYNAMICS OF CEREAL BUG POPULATIONS (EURYGASTER INTEGRICEPS PUT.) Constantin POPOV*) ABSTRACT 1977), but often the observations have been ori- ented on a single factor, clima - tic (Popov, The accumulation of reserve matter and the fat body 1980; Radjani, 1994) or biologi- cal (Popov, level among the E. integriceps species present a great 1979, 1984, 1985; Scepetilni- kova, 1963; ununiformity, both individually and from one zone to another or from one generation to another, being the Polivanova, 1994; Radjabi, 1995) without to try consequence of a complex of factors from which the the explanation of the complexity of all factors climatic and agrotechnical ones are the most important. The fat body presents a significant role into the life-cycle which influence the diapause. The paper presents of this species, constituting one of the most important a complex analysis of the physiological prepara- factors of perpetuation and numerical blasting with in- vasion role. The mean value of the fat body is different tion role, exp ressed by the fat body, on bug between sexes too, the females presenting a higher level. populations during both diapause and active life in The fat body level influences the mortality during dia- pause, the sterility and fertility, strongly influencing the postdiapause. bug population multiplication. The insects with low level of fat matter accumulations have a high mortality per- centage during diapause as well as a very low fertility. MATERIALS AND METHODS The fat body is consumed in a proportion of 25% for maturation during diapause and 50% for oviposition. The main factor of the formation of a well developed fat body The biological material consisted of Eury- is the complete rearing of adults under the best condi- gaster integriceps adults from different genera- tions. -
Bird Predation on Periodical Cicadas in Ozark Forests: Ecological Release for Other Canopy Arthropods?
Studies in Avian Biology No. 13:369-374, 1990. BIRD PREDATION ON PERIODICAL CICADAS IN OZARK FORESTS: ECOLOGICAL RELEASE FOR OTHER CANOPY ARTHROPODS? FREDERICK M. STEPHEN, GERALD W. WALLIS, AND KIMBERLY G. SMITH Abstract. Population dynamics of canopy arthropods were monitored in two upland forests in the Arkansas Ozarks during spring and summer of 1984-1986 to test whether the emergence of adult 13-year periodical cicadas on one site during late spring in 1985 would disrupt normal patterns of bird predation on canopy arthropods, resulting in ecological release for those prey populations. Canopy arthropods on foliage of oak, hickory, and eastern redcedar were sampled weekly beginning in June 1984, and April 1985 and 1986, and continuing through August in all years. We classed arthropods into four broad guilds based on foraging mode (chewers, suckers, spiders, and lepidopterous larvae) and expressed densities as number of individuals per kg of foliage sampled. Two-way analysis of variance revealed no significant treatment effects for densities of chewing, sucking, or lepidopteran larval guilds. A significant interaction of mean density between sites among years was detected for the spider guild, but not when cicadas were present, indicating that ecological release did not occur. We trace the development of the notion that bird populations are capable of affecting prey population levels, and discuss those ideas in light of our results, which suggest that birds have little impact upon their arthropod prey in Ozark forests. Kev Words: Arkansas: canonv arthronods: ecological release; guilds; insect sampling; Magicicada; Ozarks; periodical cicadas; predation. _ ’ One of the most predictable events in nature (Mugicicudu tredecim Walsh and Riley, M. -
A New Pupillarial Scale Insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in Coastal New South Wales, Australia
Zootaxa 4117 (1): 085–100 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4117.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:5C240849-6842-44B0-AD9F-DFB25038B675 A new pupillarial scale insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in coastal New South Wales, Australia PENNY J. GULLAN1,3 & DOUGLAS J. WILLIAMS2 1Division of Evolution, Ecology & Genetics, Research School of Biology, The Australian National University, Acton, Canberra, A.C.T. 2601, Australia 2The Natural History Museum, Department of Life Sciences (Entomology), London SW7 5BD, UK 3Corresponding author. E-mail: [email protected] Abstract A new scale insect, Aolacoccus angophorae gen. nov. and sp. nov. (Eriococcidae), is described from the bark of Ango- phora (Myrtaceae) growing in the Sydney area of New South Wales, Australia. These insects do not produce honeydew, are not ant-tended and probably feed on cortical parenchyma. The adult female is pupillarial as it is retained within the cuticle of the penultimate (second) instar. The crawlers (mobile first-instar nymphs) emerge via a flap or operculum at the posterior end of the abdomen of the second-instar exuviae. The adult and second-instar females, second-instar male and first-instar nymph, as well as salient features of the apterous adult male, are described and illustrated. The adult female of this new taxon has some morphological similarities to females of the non-pupillarial palm scale Phoenicococcus marlatti Cockerell (Phoenicococcidae), the pupillarial palm scales (Halimococcidae) and some pupillarial genera of armoured scales (Diaspididae), but is related to other Australian Myrtaceae-feeding eriococcids. -
Melon Aphid Or Cotton Aphid, Aphis Gossypii Glover (Insecta: Hemiptera: Aphididae)1 John L
EENY-173 Melon Aphid or Cotton Aphid, Aphis gossypii Glover (Insecta: Hemiptera: Aphididae)1 John L. Capinera2 Distribution generation can be completed parthenogenetically in about seven days. Melon aphid occurs in tropical and temperate regions throughout the world except northernmost areas. In the In the south, and at least as far north as Arkansas, sexual United States, it is regularly a pest in the southeast and forms are not important. Females continue to produce southwest, but is occasionally damaging everywhere. Be- offspring without mating so long as weather allows feeding cause melon aphid sometimes overwinters in greenhouses, and growth. Unlike many aphid species, melon aphid is and may be introduced into the field with transplants in the not adversely affected by hot weather. Melon aphid can spring, it has potential to be damaging almost anywhere. complete its development and reproduce in as little as a week, so numerous generations are possible under suitable Life Cycle and Description environmental conditions. The life cycle differs greatly between north and south. In the north, female nymphs hatch from eggs in the spring on Egg the primary hosts. They may feed, mature, and reproduce When first deposited, the eggs are yellow, but they soon parthenogenetically (viviparously) on this host all summer, become shiny black in color. As noted previously, the eggs or they may produce winged females that disperse to normally are deposited on catalpa and rose of sharon. secondary hosts and form new colonies. The dispersants typically select new growth to feed upon, and may produce Nymph both winged (alate) and wingless (apterous) female The nymphs vary in color from tan to gray or green, and offspring. -
CANDAN S., SULUDERE Z. Studies on the External Morphology of The
POLSKIE P I S M O ENTOMOLOGICZNE P O L I S H JOURNAL OF ENTOMOLOGY VOL. 75 : 369-374 Bydgoszcz 30 September 2006 Studies on the external morphology of the eggs of Eurygaster maura (Linnaeus, 1758) (Heteroptera: Scutelleridae) SELAMI CANDAN *, Z EKIYE SULUDERE ** Gazi University, Faculty of Arts and Sciences, Department of Biology, 06500 Teknikokullar, Ankara, Turkey e-mail: *[email protected], **[email protected] ABSTRACT . External morphology of egg of Eurygaster maura (LINNAEUS , 1758) was investigated by light (LM) and scanning electron microscope (SEM). The females were collected from Ankara, Aya ş, Asartepe and maintained under the laboratory conditions. Each female was shown to deposit generally 14 green eggs in a mass. The spherical shaped eggs were 1.04 mm in length and 0.96 mm in width. The first external evidence of embryonic development was the appearance of two red eye spots opposite each other beneath the aero-micropylar processes followed by appearance of a blackish T-shaped egg burster between the eye spots. Egg surface are covered with polygons. They have 20 to 22 aero-micropyles in a shape of truncated cones between polygons. KEY WORDS: Heteroptera, Scutelleridae, Eurygaster maura , chorion, external morphology, aero- micropylar processes, egg-burster, scanning electron microscope INTRODUCTION The taxonomic and phylogenetic importance of eggshell structure in pterygote insects has been demonstrated in various orders at different levels (HINTON 1981, SALKELD 1983, 1984, MARGARITIS 1985). Research on eggs of Heteroptera has been reviewed by SOUTHWOOD (1956), COBBEN (1968), and HINTON (1981). Afterwards, egg surface structure of Heteroptera species including Scutelleridae has been reported by many authors, however accurate knowledge of the egg morphology still lacks in many taxonomic groups (ESSELBAUGH 1946, GRIGOROV 1988, JAVAHERY 1994, SIMICZYJEW 1994, SULUDERE et al. -
Bilimsel Araştırma Projesi (8.011Mb)
1 T.C. GAZİOSMANPAŞA ÜNİVERSİTESİ Bilimsel Araştırma Projeleri Komisyonu Sonuç Raporu Proje No: 2008/26 Projenin Başlığı AMASYA, SİVAS VE TOKAT İLLERİNİN KELKİT HAVZASINDAKİ FARKLI BÖCEK TAKIMLARINDA BULUNAN TACHINIDAE (DIPTERA) TÜRLERİ ÜZERİNDE ÇALIŞMALAR Proje Yöneticisi Prof.Dr. Kenan KARA Bitki Koruma Anabilim Dalı Araştırmacı Turgut ATAY Bitki Koruma Anabilim Dalı (Kasım / 2011) 2 T.C. GAZİOSMANPAŞA ÜNİVERSİTESİ Bilimsel Araştırma Projeleri Komisyonu Sonuç Raporu Proje No: 2008/26 Projenin Başlığı AMASYA, SİVAS VE TOKAT İLLERİNİN KELKİT HAVZASINDAKİ FARKLI BÖCEK TAKIMLARINDA BULUNAN TACHINIDAE (DIPTERA) TÜRLERİ ÜZERİNDE ÇALIŞMALAR Proje Yöneticisi Prof.Dr. Kenan KARA Bitki Koruma Anabilim Dalı Araştırmacı Turgut ATAY Bitki Koruma Anabilim Dalı (Kasım / 2011) ÖZET* 3 AMASYA, SİVAS VE TOKAT İLLERİNİN KELKİT HAVZASINDAKİ FARKLI BÖCEK TAKIMLARINDA BULUNAN TACHINIDAE (DIPTERA) TÜRLERİ ÜZERİNDE ÇALIŞMALAR Yapılan bu çalışma ile Amasya, Sivas ve Tokat illerinin Kelkit havzasına ait kısımlarında bulunan ve farklı böcek takımlarında parazitoit olarak yaşayan Tachinidae (Diptera) türleri, bunların tanımları ve yayılışlarının ortaya konulması amaçlanmıştır. Bunun için farklı böcek takımlarına ait türler laboratuvarda kültüre alınarak parazitoit olarak yaşayan Tachinidae türleri elde edilmiştir. Kültüre alınan Lepidoptera takımına ait türler içerisinden, Euproctis chrysorrhoea (L.), Lymantria dispar (L.), Malacosoma neustrium (L.), Smyra dentinosa Freyer, Thaumetopoea solitaria Freyer, Thaumetopoea sp. ve Vanessa sp.,'den parazitoit elde edilmiş, -
The Semiaquatic Hemiptera of Minnesota (Hemiptera: Heteroptera) Donald V
The Semiaquatic Hemiptera of Minnesota (Hemiptera: Heteroptera) Donald V. Bennett Edwin F. Cook Technical Bulletin 332-1981 Agricultural Experiment Station University of Minnesota St. Paul, Minnesota 55108 CONTENTS PAGE Introduction ...................................3 Key to Adults of Nearctic Families of Semiaquatic Hemiptera ................... 6 Family Saldidae-Shore Bugs ............... 7 Family Mesoveliidae-Water Treaders .......18 Family Hebridae-Velvet Water Bugs .......20 Family Hydrometridae-Marsh Treaders, Water Measurers ...22 Family Veliidae-Small Water striders, Rime bugs ................24 Family Gerridae-Water striders, Pond skaters, Wherry men .....29 Family Ochteridae-Velvety Shore Bugs ....35 Family Gelastocoridae-Toad Bugs ..........36 Literature Cited ..............................37 Figures ......................................44 Maps .........................................55 Index to Scientific Names ....................59 Acknowledgement Sincere appreciation is expressed to the following individuals: R. T. Schuh, for being extremely helpful in reviewing the section on Saldidae, lending specimens, and allowing use of his illustrations of Saldidae; C. L. Smith for reading the section on Veliidae, checking identifications, and advising on problems in the taxon omy ofthe Veliidae; D. M. Calabrese, for reviewing the section on the Gerridae and making helpful sugges tions; J. T. Polhemus, for advising on taxonomic prob lems and checking identifications for several families; C. W. Schaefer, for providing advice and editorial com ment; Y. A. Popov, for sending a copy ofhis book on the Nepomorpha; and M. C. Parsons, for supplying its English translation. The University of Minnesota, including the Agricultural Experi ment Station, is committed to the policy that all persons shall have equal access to its programs, facilities, and employment without regard to race, creed, color, sex, national origin, or handicap. The information given in this publication is for educational purposes only. -
Chapter 12. Estimating the Host Range of the Tachinid Trichopoda Giacomellii, Introduced Into Australia for Biological Control of the Green Vegetable Bug
__________________________________ ASSESSING HOST RANGES OF PARASITOIDS AND PREDATORS CHAPTER 12. ESTIMATING THE HOST RANGE OF THE TACHINID TRICHOPODA GIACOMELLII, INTRODUCED INTO AUSTRALIA FOR BIOLOGICAL CONTROL OF THE GREEN VEGETABLE BUG M. Coombs CSIRO Entomology, 120 Meiers Road, Indooroopilly, Queensland, Australia 4068 [email protected] BACKGROUND DESCRIPTION OF PEST INVASION AND PROBLEM Nezara viridula (L.) is a cosmopolitan pest of fruit, vegetables, and field crops (Todd, 1989). The native geographic range of N. viridula is thought to include Ethiopia, southern Europe, and the Mediterranean region (Hokkanen, 1986; Jones, 1988). Other species in the genus occur in Africa and Asia (Freeman, 1940). First recorded in Australia in 1916, N. viridula soon be- came a widespread and serious pest of most legume crops, curcubits, potatoes, tomatoes, pas- sion fruit, sorghum, sunflower, tobacco, maize, crucifers, spinach, grapes, citrus, rice, and mac- adamia nuts (Hely et al., 1982; Waterhouse and Norris, 1987). In northern Victoria, central New South Wales, and southern Queensland, N. viridula is a serious pest of soybeans and pecans (Clarke, 1992; Coombs, 2000). Immature and adult bugs feed on vegetative buds, devel- oping and mature fruits, and seeds, causing reductions in crop quality and yield. The pest status of N. viridula in Australia is assumed to be partly due to the absence of parasitoids of the nymphs and adults. No native Australian tachinids have been found to parasitize N viridula effectively, although occasional oviposition and development of some species may occur (Cantrell, 1984; Coombs and Khan, 1997). Previous introductions of biological control agents to Australia for control of N. viridula include Trichopoda pennipes (Fabricius) and Trichopoda pilipes (Fabricius) (Diptera: Tachinidae), which are important parasitoids of N.