Locust and Grasshopper Outbreaks in Zululand Sugarcane, Kwazulu-Natal
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Character Evolution and Microbial Community Structure in a Host-Associated Grasshopper
CHARACTER EVOLUTION AND MICROBIAL COMMUNITY STRUCTURE IN A HOST-ASSOCIATED GRASSHOPPER by TYLER JAY RASZICK B.S. University of Florida, 2010 A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in the Department of Biology in the College of Sciences at the University of Central Florida Orlando, Florida Spring Term 2014 © 2014 Tyler J. Raszick ii ABSTRACT The spotted bird grasshopper, Schistocerca lineata Scudder (Orthoptera: Acrididae), is a widely distributed species found throughout most of the continental United States and southern Canada. This species is known to be highly variable in morphology, with many distinct ecotypes across its native range. These ecotypes display high levels of association with type-specific host plants. Understanding the evolutionary relationships among different ecotypes is crucial groundwork for studying the process of ecological differentiation. I examine four ecotypes from morphological and phylogeographic perspectives, and look for evidence of distinct evolutionary lineages within the species. I also begin to explore the potential role of the microbial community of these grasshoppers in ecological divergence by using 454 pyrosequencing to see if the microbial community structure reflects the ecology of the grasshoppers. I find support for a distinct aposematic lineage when approaching the data from a phylogeographic perspective and also find that this ecotype tends to harbor a unique bacterial community, different from that of a single other ecotype. iii ACKNOWLEDGMENTS I would like to acknowledge my advisor H. Song of the University of Central Florida for mentorship throughout my degree, as well as my thesis committee, K. Fedorka and E. -
Studies on the Nymphal Aggregation Pheromone of Malagasy
STUDIES ON THE NYMPHAL AGGREGATION PHEROMONE OF MALAGASY MIGRATORY LOCUST, LOCUSTA MIGRATORIA CAPITO (SAUSSURE, 1884) AND ITS EFFECTS ON ADULT MATURATION VICTOR RAZAFINDRANAIVO DOCTOR OF PHILOSOPHY (Zoology) JOMO KENYATTA UNIVERSITY OF AGRICULTURE AND TECHNOLOGY 2010 Studies on the nymphal aggregation pheromone of Malagasy Migratory Locust, Locusta migratoria capito (Saussure, 1884) and its effects on adult maturation. Victor Razafindranaivo A thesis submitted in fulfilment for the degree of Doctor of Philosophy in Zoology in the Jomo Kenyatta University of Agriculture and Technology 2010 DECLARATION This thesis is my original work and has not been presented for a degree in any other University Signature --------------------------------- Date ------------------------------------------------ Victor Razafindranaivo This thesis has been submitted with our approval as university supervisors Signature --------------------------------- Date ------------------------------------------------ Dr. Helen Lydia Kutima JKUAT, Kenya Signature --------------------------------- Date ------------------------------------------------ Prof. Muniru K. Tsanuo Pwani University College, Kenya Signature --------------------------------- Date ------------------------------------------------ Prof. Ahmed Hassanali KU, Kenya Signature --------------------------------- Date ------------------------------------------------ Dr. Peter G. N. Njagi International Centre of Insect Physiology and Ecology, Kenya ii DEDICATION I dedicated this thesis to my late mother, who struggled -
Elements for the Sustainable Management of Acridoids of Importance in Agriculture
African Journal of Agricultural Research Vol. 7(2), pp. 142-152, 12 January, 2012 Available online at http://www.academicjournals.org/AJAR DOI: 10.5897/AJAR11.912 ISSN 1991-637X ©2012 Academic Journals Review Elements for the sustainable management of acridoids of importance in agriculture María Irene Hernández-Zul 1, Juan Angel Quijano-Carranza 1, Ricardo Yañez-López 1, Irineo Torres-Pacheco 1, Ramón Guevara-Gónzalez 1, Enrique Rico-García 1, Adriana Elena Castro- Ramírez 2 and Rosalía Virginia Ocampo-Velázquez 1* 1Department of Biosystems, School of Engineering, Queretaro State University, C.U. Cerro de las Campanas, Querétaro, México. 2Department of Agroecology, Colegio de la Frontera Sur, San Cristóbal de las Casas, Chiapas, México. Accepted 16 December, 2011 Acridoidea is a superfamily within the Orthoptera order that comprises a group of short-horned insects commonly called grasshoppers. Grasshopper and locust species are major pests of grasslands and crops in all continents except Antarctica. Economically and historically, locusts and grasshoppers are two of the most destructive agricultural pests. The most important locust species belong to the genus Schistocerca and populate America, Africa, and Asia. Some grasshoppers considered to be important pests are the Melanoplus species, Camnula pellucida in North America, Brachystola magna and Sphenarium purpurascens in northern and central Mexico, and Oedaleus senegalensis and Zonocerus variegatus in Africa. Previous studies have classified these species based on specific characteristics. This review includes six headings. The first discusses the main species of grasshoppers and locusts; the second focuses on their worldwide distribution; the third describes their biology and life cycle; the fourth refers to climatic factors that facilitate the development of grasshoppers and locusts; the fifth discusses the action or reaction of grasshoppers and locusts to external or internal stimuli and the sixth refers to elements to design management strategies with emphasis on prevention. -
Morphology and Development of Oocyte and Follicle Resorption Bodies in the Lubber Grasshopper, Romalea Microptera (Beauvois)
S.V. SUNDBERG, M.H. LUONG-SKOVMANDJournal of Orthoptera AND D.W. Research, WHITMAN June 2001, 10 (1): 39-5139 Morphology and development of oocyte and follicle resorption bodies in the Lubber grasshopper, Romalea microptera (Beauvois) STEVEN V. SUNDBERG, MY HANH LUONG-SKOVMAND AND DOUGLAS W. WHITMAN [SVS, DWW] Behavior, Ecology, Evolution, & Systematic Section, 4120 Department of Biological Sciences, Illinois State University, Normal, IL 61790-4120, USA e-mail: [email protected] [MHLS] CIRAD, Centre de Cooperation Internationale en Recherche Agronomique pour le Developpement (Prifas) BP 5035 - 34032 Montpellier cedex 1 - France e-mail: [email protected] Abstract We describe the development and appearance of Follicle Resorption ovocyte, produisent un corps de régression de couleur jaune orangé. Bodies (FRBs) and Oocyte Resorption Bodies (ORBs) in the Le nombre de traces de ponte est égal au nombre d’oeufs pondus et grasshopper Romalea microptera (= guttata), and demonstrate that le nombre de corps de régression au nombre d’ovocytes ayant these structures can be used to determine the past ovipositional and régressé. Les R. microptera en bonne santé et nourris en abondance environmental history of females. In R. microptera, one resorption résorbent environ le quart de leur ovocytes en croissance. La privation body is deposited at the base of each ovariole following each de nourriture ou le stress physiologique entrainent une gonotropic cycle. These structures are semi-permanent, and remain augmentation du taux de régression ovocytaire et par conséquent distinct for at least 8 wks and two additional ovipositions. Ovarioles du nombre de corps de régression (ORB). Si l’on compte les traces that ovulate a mature, healthy oocyte, produce a cream-colored de ponte et les corps de régression dans chaque ovariole, on obtient FRB. -
Susceptibility of Five Pearl Ecotypes to the Nymphal I Locusta Migratoria
Sudan University of Science and Technology College of Graduate Studies Susceptibility of five pearl millet (Pennisetum glaucum L. Ecotypes to the nymphal instars of the Migratory locust Locusta migratoria migratorioides (Reiche and Farmaire) infestation. By Kholdi Fathi Salim Gomaa B.Sc. in Agricultural studies, Honors (Plant Protection). Sudan University of Science & technology. 2010. A dissertation Submitted to the Sudan University of Science & technology in Partial Fulfillment of the Requirements for the Degree of Master of Science in Plant Protection. Supervisor. Prof: Magzoub Omer Bashir. Department of Crop Protection. Faculty of Agriculture University of Khartoum June, 2015. INCEPTION ﻗﺎل ﺗﻌﺎﻟﻰ: (اﻷﻋﺮاف : 133 ) {ﺧُﺸﱠﻌﺎً أَﺑْﺼَﺎرُﻫُﻢْ ﻳَﺨْﺮُﺟُﻮنَ ﻣِﻦَ اﻟْﺄَﺟْﺪَاثِ ﻛَﺄَﻧﱠﻬُﻢْ ﺟَﺮَادٌ ﻣﱡﻨﺘَﺸِﺮٌ } (اﻟﻘﻤﺮ : 7 ) I DEDICATION To my beloved mother. To my dear father. To my dear and faithful uncle Nassir Elsayed. To my uncles, aunts, brothers, sisters and cousins. II ACKNOWLEDGEMENTS In the beginning I render my acknowledgement to the Almighty Allah. I am indebted to and express my deepest thanks, sincere gratitude and appreciation to my supervisor Professor Magzoub Omer Bashir for his continuous guidance, suggestions and encouragement throughout the period of this study. I would like to thank all staff members of Plant Protection Department, Sudan University of Science and Technology and staff members of Crop Protection Department, University of Khartoum. My thanks also extend to my colleague Salih Nurain who helped me in literature, data analysis and thesis preparing. Also thanks to Dr. Jaffar Farah at crop production of (SUST), Dr. Rabei Abdelmagid from Ministry of Agriculture and to my colleague Abdelhakim Shogar. At Last but not least I am greatly indebted to all those whom I may have forgotten, I offer my sincere apologies. -
Studies on the Biology and Morphology
STUDIES ON THE BIOLOGY AND MORPHOLOGY OF SCHISTOCERCA OBSctTRA. FABR~ OCT ~-'/ 1939 \,. STODI]S ON fflE BIOLOGY AND UORPHOLOGf OF SOHISTOCERCA OBSCURA FABR. By LESTER GLEN DUCK 1, Bachelor ot Science Northwestern State Teacher's College Alva, Oklahoma. A THESIS Submitted to the Department of" Entomology Oklahoma .Agricultural and Mechanical College In Partial J!ultillment of" the Requirements FOr the Degree ot MASTER OF SCIENCE C 1939 o" -: o "e ((.f!) ~ r ~ 0 0 , 0 ,, {,] 0 . 0 0 0' 0 ,._< )",-- : ,." - ' ' O r c> o " O ,, C> 0 ~ ·'" "•i" U U O D 0 0 ' 0 C ,-- 0 0 <l 0 r: ' Cl , 0 O O ' 0 O C' OQ<.,1:~ ll~ STUDIES ON mE BIOLOGY AND MORPHOLOGY OF SCHISTOCERCA OBSCURA. J'ABR. CCLLEGE OCT ;.;,'/ 1939 .._ STUDIES ON 'IRE BIOLOGY AND MORPHOLOGY OF SOHISTOCERCA OBSCURA ll"ABR. By LESTER GLEN DUCK I\ Bachelor of Science Northwestern State Teacher's College Alva, Oklahoma 1937 A THESIS Submitted to the Department of Entomology Oklahoma Agricultural and Mechanical College In Partial Jfu.lfillment of the Requirements For the Degree of 0 MASTER OF SCIENCE : e. r:, 0 J 0 • , ... ,"- ~ ~ 1939 0-'"';_, 0~0°,~ IJO 1 0 0 0 _, ·~ 0 ' c~ O ()" c_, O O D c 0 (' C~ 0 <:I Or 11 OCT ~11939 l APPROVED: In Charge of Thesis Head or Department ot 1!ntomology Dean or Graduate School 119466 111 PREFACE This thesis grew out ot a suggestion b1 Professor F. A. !'enton concern ing the need tor information on certain members of the Orthopteran genus Schistocerca. As the work progressed, it became Dl)re and more evident that a thorough understanding ot the genus can coma only through a close e:xam.1.nation of the biology of each species. -
Grasshoppers of the Choctaw Nation in Southeast Oklahoma
Oklahoma Cooperative Extension Service EPP-7341 Grasshoppers of the Choctaw Nation in Southeast OklahomaJune 2021 Alex J. Harman Oklahoma Cooperative Extension Fact Sheets Graduate Student are also available on our website at: extension.okstate.edu W. Wyatt Hoback Associate Professor Tom A. Royer Extension Specialist for Small Grains and Row Crop Entomology, Integrated Pest Management Coordinator Grasshoppers and Relatives Orthoptera is the order of insects that includes grasshop- pers, katydids and crickets. These insects are recognizable by their shape and the presence of jumping hind legs. The differ- ences among grasshoppers, crickets and katydids place them into different families. The Choctaw recognize these differences and call grasshoppers – shakinli, crickets – shalontaki and katydids– shakinli chito. Grasshoppers and the Choctaw As the men emerged from the hill and spread throughout the lands, they would trample many more grasshoppers, killing Because of their abundance, large size and importance and harming the orphaned children. Fearing that they would to agriculture, grasshoppers regularly make their way into all be killed as the men multiplied while continuing to emerge folklore, legends and cultural traditions all around the world. from Nanih Waiya, the grasshoppers pleaded to Aba, the The following legend was described in Tom Mould’s Choctaw Great Spirit, for aid. Soon after, Aba closed the passageway, Tales, published in 2004. trapping many men within the cavern who had yet to reach The Origin of Grasshoppers and Ants the surface. In an act of mercy, Aba transformed these men into ants, During the emergence from Nanih Waiya, grasshoppers allowing them to rule the caverns in the ground for the rest of traveled with man to reach the surface and disperse in all history. -
Orthoptera: Acrididae
FOOD PLAOT PREFERENCES OF GRASSHOPPERS (ORTOOPTERAt ACRIDIDAE) OF SELECTED PLANTED PASTURES IN EASTERN KANSAS by JAMES DALE LAMBLEY B. S., Kansas State University, ftonhattan, 1965 A THESIS submitted in partial fulfillment of the requirements for the degree MASTER OF SCIENCE Department of Entomology Kansas State University Manhattan, Kansas 1967 Approved byt Major Professor LP alW ii IP C-'-5- TABLE OF CONTENTS ^ INTRODUCTION • ^ REVIEV OF LITERATURE MTHRIALS AND METHODS ^ ^ Study Area '° Field and Laboratory Studies RESULTS AND DISCUSSION 21 Acridinae 1 22 Oedipodinae ' 1 9S Cyrtacanthacridinae SUWJ'ARY 128 LITERAPJRS CITED. 131 ACKKO'.VLEDGKENTS '•^® APPENDIX 1^° INTOODUCnON The purpose of this study, near Manhattan, Kansas, during 1965 and 1966, was to increase knowledge of the feeding and behavior of grasshoppers in of the planted (tame) pastures. Emphasis was placed on the feeding habits more common species. Great Grasshoppers have long been considered serious plant pests in the of rangelands Plains area of the United States. Loss in production potential (including pasture grass and other forage) has been estimated to be not include $80,000,000 per year for 1959 and 1960 (Anon., 1965). This does funds spent for grasshopper control. methods of Consequently, m-jch of the research has been directed towards biology immediate direct control. Little basic research dealing with the less on and ecology of grasshoppers of rangeland has been done and even from such planted pasture species. Neglect in basic research has resulted from cropland; factors as (l) lower economic return from grassland than than in cropland: and, (2) insect damage is often less apparent in grassland intensive (3) recent recognition of grasslands as resources deserving scientific investigation. -
New Canadian and Ontario Orthopteroid Records, and an Updated Checklist of the Orthoptera of Ontario
Checklist of Ontario Orthoptera (cont.) JESO Volume 145, 2014 NEW CANADIAN AND ONTARIO ORTHOPTEROID RECORDS, AND AN UPDATED CHECKLIST OF THE ORTHOPTERA OF ONTARIO S. M. PAIERO1* AND S. A. MARSHALL1 1School of Environmental Sciences, University of Guelph, Guelph, Ontario, Canada N1G 2W1 email, [email protected] Abstract J. ent. Soc. Ont. 145: 61–76 The following seven orthopteroid taxa are recorded from Canada for the first time: Anaxipha species 1, Cyrtoxipha gundlachi Saussure, Chloroscirtus forcipatus (Brunner von Wattenwyl), Neoconocephalus exiliscanorus (Davis), Camptonotus carolinensis (Gerstaeker), Scapteriscus borellii Linnaeus, and Melanoplus punctulatus griseus (Thomas). One further species, Neoconocephalus retusus (Scudder) is recorded from Ontario for the first time. An updated checklist of the orthopteroids of Ontario is provided, along with notes on changes in nomenclature. Published December 2014 Introduction Vickery and Kevan (1985) and Vickery and Scudder (1987) reviewed and listed the orthopteroid species known from Canada and Alaska, including 141 species from Ontario. A further 15 species have been recorded from Ontario since then (Skevington et al. 2001, Marshall et al. 2004, Paiero et al. 2010) and we here add another eight species or subspecies, of which seven are also new Canadian records. Notes on several significant provincial range extensions also are given, including two species originally recorded from Ontario on bugguide.net. Voucher specimens examined here are deposited in the University of Guelph Insect Collection (DEBU), unless otherwise noted. New Canadian records Anaxipha species 1 (Figs 1, 2) (Gryllidae: Trigidoniinae) This species, similar in appearance to the Florida endemic Anaxipha calusa * Author to whom all correspondence should be addressed. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Pathogen-Induced Change in the Phase State of Locust Offspring
Submitted to PNAS Classification: Biological Sciences - Ecology Fever impacts on host life history traits, but is this a cost? Sam L. Elliot1, Charlotte M. Horton1, Simon Blanford1,2 and Matthew B. Thomas1,3 Author affiliation: 1 NERC Centre for Population Biology, Imperial College London, Silwood Park Campus, Ascot, Berks, SL5 7PY, UK 2 Institute of Cell, Animal and Population Biology, Ashworth Laboratories, West Mains Road, University of Edinburgh, Edinburgh, EH9 3JT, UK 3 Department of Agricultural Sciences, Imperial College London, Wye Campus, Wye, Ashford, Kent, TN25 5AH, UK Corresponding author: Sam Elliot, NERC Centre for Population Biology, Imperial College London, Silwood Park Campus, Ascot, Berks, SL5 7PY, UK. Tel: +44 (0)20 7594 2529. Fax: +44 (0)1344 873173. E-mail: [email protected] Manuscript information: 11 text pages (16 total), 1 figure Word and character counts: 273 words in Abstract 25, 675 characters in paper (incl. spaces) ABSTRACT Fever is one mechanism by which animals may defend themselves against pathogens but, as with other defenses, may have consequences for the host. In ectotherms such as the desert locust (Schistocerca gregaria), fever temperatures are attained through modified behavioural thermoregulation. We have previously demonstrated that the fitness benefits of behavioural fever in S. gregaria can be substantial: a fever temperature just 2-4°C higher than the normal can make the difference between zero and near-normal reproduction when infected with a fungal pathogen. Here we examined whether there are costs associated with these elevated temperatures by holding adult, gregarious S. gregaria at elevated temperatures for one or five hours per day and for ten or twenty days. -
Wasps and Bees in Southern Africa
SANBI Biodiversity Series 24 Wasps and bees in southern Africa by Sarah K. Gess and Friedrich W. Gess Department of Entomology, Albany Museum and Rhodes University, Grahamstown Pretoria 2014 SANBI Biodiversity Series The South African National Biodiversity Institute (SANBI) was established on 1 Sep- tember 2004 through the signing into force of the National Environmental Manage- ment: Biodiversity Act (NEMBA) No. 10 of 2004 by President Thabo Mbeki. The Act expands the mandate of the former National Botanical Institute to include respon- sibilities relating to the full diversity of South Africa’s fauna and flora, and builds on the internationally respected programmes in conservation, research, education and visitor services developed by the National Botanical Institute and its predecessors over the past century. The vision of SANBI: Biodiversity richness for all South Africans. SANBI’s mission is to champion the exploration, conservation, sustainable use, appreciation and enjoyment of South Africa’s exceptionally rich biodiversity for all people. SANBI Biodiversity Series publishes occasional reports on projects, technologies, workshops, symposia and other activities initiated by, or executed in partnership with SANBI. Technical editing: Alicia Grobler Design & layout: Sandra Turck Cover design: Sandra Turck How to cite this publication: GESS, S.K. & GESS, F.W. 2014. Wasps and bees in southern Africa. SANBI Biodi- versity Series 24. South African National Biodiversity Institute, Pretoria. ISBN: 978-1-919976-73-0 Manuscript submitted 2011 Copyright © 2014 by South African National Biodiversity Institute (SANBI) All rights reserved. No part of this book may be reproduced in any form without written per- mission of the copyright owners. The views and opinions expressed do not necessarily reflect those of SANBI.