Grasshopper Identification Guide for Cropland Grasshoppers Summer Feeding Species
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Grasshoppers
Grasshoppers Orthoptera: Acrididae Plains Lubber Pictured grasshoppers Great crested grasshopper Snakeweed grasshoppers Primary Pest Grasshoppers • Migratory grasshopper • Twostriped grasshopper • Differential grasshopper • Redlegged grasshopper • Clearwinged grasshopper Twostriped Grasshopper, Melanoplus bivittatus Redlegged Grasshopper, Melanoplus femurrubrum Differential Grasshopper, Melanoplus differentialis Migratory Grasshopper, Melanoplus sanguinipes Clearwinged Grasshopper Camnula pellucida Diagram courtesy of Alexandre Latchininsky, University of Wyoming Photograph courtesy of Jean-Francoise Duranton, CIRAD Grasshoppers lay pods of eggs below ground Grasshopper Egg Pods Molting is not Linedfor wimps! bird grasshopper molting to adult stage Grasshopper Nymphs Some grasshoppers found in winter and early spring Velvet-striped grasshopper – a common spring species Grasshopper Controls • Weather (rainfall mediated primarily) • Natural enemies – Predators, diseases • Treatment of breeding areas • Biological controls • Row covers Temperature and rainfall are important mortality factors Grasshoppers and Rainfall Moisture prior to egg hatch generally aids survival – Newly hatched young need succulent foliage Moisture after egg hatch generally reduces problems – Assists spread of diseases – Allows for plenty of food, reducing competition for rangeland and crops Grasshopper predators Robber Flies Larvae of many blister beetles develop on grasshopper egg pods Blister beetle larva Fungus-killed Grasshoppers Pathogen: Entomophthora grylli Mermis -
Spur-Throated Grasshoppers of the Canadian Prairies and Northern Great Plains
16 Spur-throated grasshoppers of the Canadian Prairies and Northern Great Plains Dan L. Johnson Research Scientist, Grassland Insect Ecology, Lethbridge Research Centre, Agriculture and Agri-Food Canada, Box 3000, Lethbridge, AB T1J 4B1, [email protected] The spur-throated grasshoppers have become the most prominent grasshoppers of North Ameri- can grasslands, not by calling attention to them- selves by singing in the vegetation (stridulating) like the slant-faced grasshoppers, or by crackling on the wing (crepitating) like the band-winged grasshoppers, but by virtue of their sheer num- bers, activities and diversity. Almost all of the spur-throated grasshoppers in North America are members of the subfamily Melanoplinae. The sta- tus of Melanoplinae is somewhat similar in South America, where the melanopline Dichroplus takes the dominant role that the genus Melanoplus pated, and hiding in the valleys?) scourge that holds in North America (Cigliano et al. 2000). wiped out so much of mid-western agriculture in The biogeographic relationships are analysed by the 1870’s. Chapco et al. (2001). The grasshoppers are charac- terized by a spiny bump on the prosternum be- Approximately 40 species of grasshoppers in tween the front legs, which would be the position the subfamily Melanoplinae (mainly Tribe of the throat if they had one. This characteristic is Melanoplini) can be found on the Canadian grass- easy to use; I know elementary school children lands, depending on weather and other factors af- who can catch a grasshopper, turn it over for a fecting movement and abundance. The following look and say “melanopline” before grabbing the notes provide a brief look at representative next. -
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. -
Food Plants of Melanoplus Femurrubrum Femurrubrum (Degeer
FOOD PLANTS OF MELANOPLUS FEMURRUERU?' ^'? URRUBRUM (DEGEER) THE BLUESTEM GRASS REGION OF KANSAS by ORLO KENNETH JANTZ I B. S., Kansas State University, 1957 A MASTER 1 S THESIS submitted in partial fulfillment of the requirements for the degree MASTER OF SCIENCE Department of Entomology KANSAS STATE UNIVERSITY Manhattan, Kansas 1962 LD 2(ofc8 T^ \%a ii cm TABLE c £ OF CONTENTS INTRODUCTION 1 REVIEW OF LITERATURE 2 MATERIALS AND METHODS 5 RESULTS AND DISCUSSION 10 SUMMARY 22 ACKNOWLEDGMENTS 77 LITERATURE 78 INTRODUCTION The species of grasshoppers in a given area and their populations are determined to a considerable extent by food plants. Food prefer- ences and relationships of grasshopper species and plant species in pastures of the Great Plains are not well understood. Cage studies on plant food preferences are one of the current phases of the grasshopper project which has been in progress since 1957 and is part of Regional Project NC-52 on factors influencing the distribution and abundance of grasshoppers. The Kansas portion of the project involves a study of a series of habitats within a bluestem grass range, the Donaldson Pastures, near Manhattan, Kansas. Nine pastures, each under different experimental treatments, are studied. Three of these pastures are included in an intensity-of-grazing treat- ment, three in a deferred grazing treatment and three in a time-of- spring-burning treatment. Range sites *ithin each of the nine treat- ments are: limestone breaks, ordinary upland, and clay upland. Axnett (i960) was the initial investigator. Largest grasshopper populations were found on the early spring burned and the heaviest grazed pastures. -
A Spur-Throat Grasshopper (Melanoplus Lemhiensis)
A Spur-throat Grasshopper Melanoplus lemhiensis Insecta — Orthoptera — Acrididae CONSERVATION STATUS / CLASSIFICATION Rangewide: Critically imperiled/Imperiled (G1G2) Statewide: Critically imperiled (S1) ESA: No status USFS: Region 1: No status; Region 4: No status BLM: No status IDFG: Not classified BASIS FOR INCLUSION Lack of essential information pertaining to status; Idaho endemic. TAXONOMY Hebard (1935) considered this species to be morphologically similar to M. artemisiae and M. salmonis. Hebard (1935) reported that both M. idaho and M. lemhiensis were collected on the same date and at the same location and that he did not recognize, in the field, that the observed male and female M. idaho individuals were different from M. lemhiensis. In later examination and description of both new species, M. idaho and M. lemhiensis, Hebard placed M. idaho in the montanus species group and M. lemhiensis in the artemisiae species group. Strohecker (1963) retained M. lemhiensis in the artemisiae species group. DISTRIBUTION AND ABUNDANCE This grasshopper is endemic to Idaho. The taxon is known from 1 locality in Lemhi County. No record of this species since its original collection during 1928 (Hebard 1935) is known. POPULATION TREND No data are available to suggest population trend. The species has not been recorded since 1928. HABITAT AND ECOLOGY Hebard (1935) reported that the series of specimens he collected were “secured on steep slopes of rock fragments thickly overgrown with sagebrush. The species was common only on the steepest upper slopes where there were many tufts of a fine, dry, yellow grass. The insect is a powerful though slow leaper …, but instead of immediately jumping into another bush individuals usually leaped about in the open and were consequently much easier to capture. -
The Food Insects Newsletter Home
Volume 2 No.3 Index for A Place to Browse - The Food Insects Newsletter Home THE FOOD INSECTS NEWSLETTER NOVEMBER 1989 VOLUME II, NO. 3 CHITIN: A Magic Bullet? Editor's Note: Whole dried insects are about 10 percent chitin, of chitin that are parallel to the upper surface of the cell. As more or less. Although chitin presents problems of the process continues, the newer layers are secreted in a digestibility and assimilability in monogastric animals, it and parallel fashion but the orientation of the fibrils has been its derivatives, particularly chitosan, possess properties that slightly rotated. This can be best visualized by placing one are of increasing interest in medicine, industry and agriculture. hand over the other in a parallel fashion and outstretching the If the time should come when protein concentrates from fingers. Keeping the bottom hand in the same plane, rotate it insects are acceptable and produced on a large scale, the chitin slightly so that looking from the top side the fingers form a byproduct could be of significant value. At the editor's request grid. As your hands rotate through 180°, note the spatial Dr. Walter G. Goodman. professor of developmental biology orientation between the fingers of the upper and lower hands. in the Department of Entomology, University of Wisconsin, On a smaller scale, a similar process occurs in the newly kindly agreed to prepare a short article for the Newsletter on secreted layers of fibrils. Thus, micrograph cross-section the characteristics of chitin and some of its potential through the cuticle resembles the end-view of plywood due to applications. -
ARTICULATA 1993 8(2): 1 -22 SYSTEMATIK to the Knowledge Of
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Articulata - Zeitschrift der Deutschen Gesellschaft für Orthopterologie e.V. DGfO Jahr/Year: 1993 Band/Volume: 8_2_1993 Autor(en)/Author(s): Storozhenko Sergey Artikel/Article: To the knowledge of the tribe Melanoplini (Orthoptera, Acrididae: Catantopinae) of the Eastern Palearctlca 1-22 Deutschen Gesellschaft für Orthopterologie e.V.; download http://www.dgfo-articulata.de/ ARTICULATA 1993 8(2): 1 -22 SYSTEMATIK To the knowledge of the tribe Melanoplini (Orthoptera, Acrididae: Catantopinae) of the Eastern Palearctlca Sergey Storozhenko Abstract Data on the grasshoppers of the tribe Melanoplini SCUDDER, 1897 (= Podismini JACOBSON, 1905 = Parapodisminae INOUE, 1985, syn. n) of Eastern Palearctica are given. Podisma kanoi sp. n. and Podisma sapporensis ashibetsuensis ssp. n. from Japan are described. The new synonyms are established: Rhinopodisma MISTSHENKO, 1954 = Aserratus HUANG, 1981, syn. n., Sinopodisma CHANG, 1940 = Pedopodisma ZHENG, 1980, syn. n., Parapodisma MISTSHENKO, 1947 = Pseudoparapodisma INOUE, 1985, syn. n., Monopterus FISCHER-WALDHEIM, 1846 = Bohemanella RAMME, 1951, syn.n. Tribe Melanoplini SCUDDER, 1897 Type genus: Melanoplus STAL, 1873. Notes The tribe Melanoplini was established by S.SCUDDER (1897) as a group Melanopli. JACOBSON (1905) proposed Podismini as a new name for this group. In the most modem classification the position of tribe Melanoplini is following: MISTSHENKO (1952) considered it as a tribe Podismini of subfamily Catanto pinae (Acrididae); UVAROV (1966) as Catantopinae (without division on tribes); DIRSH (1975) as subfamily Podisminae of family Catantopidae; HARZ (1975) as tribe Podismini of subfamily Catantopinae (Acrididae); VICKERY & KEVAN (1983) as subfamily Melanoplinae of family Acrididae with two tribes (Melanoplini and Podismini) and YIN (1984) as subfamily Podisminae of family Oedipodidae. -
Redlegged Grasshopper
Pest Profile Photo credit: Russ Ottens, University of Georgia, Bugwood.org Common Name: Redlegged Grasshopper Scientific Name: Melanoplus femurrubrum Order and Family: Orthoptera and Acrididae Size and Appearance: Redlegged grasshoppers range in size, from ¾ to 1-inch long. They are variable in color but they can be identified by their reddish-brown color with a yellow underside, their bright red tibia on the hind legs, and a black colored line right behind the eyes. Nymphs resemble the adults, but are smaller in size and have a solid black stripe that runs across the sides of the head and along the sides of the thorax. Length (mm) Appearance Egg Light brown colored; elongate shaped; eggs are laid in soil in clusters in earthen cell; females lay 25-30 eggs in a cluster; hatch late spring to summer. Larva/Nymph 4-6mm, 1st Resemble adults but smaller; have solid black stripe running instar across sides of head and along sides of thorax; wings absent, but have developing wing buds in later instars; 5 instars. Adult 17-30mm Variable in color from yellow, green, dark brown, or reddish brown; yellow underside; bright red tibia on hind legs; black line behind eyes; black herringbone pattern on femur of back legs. Pupa (if applicable) Type of feeder (Chewing, sucking, etc.): Nymphs and Adults: Chewing. Host plant/s: They have a wide range of host plants; grasses particularly favored, but they can also damage garden plants and grain crops. More commonly damaged garden plants include bean, leafy vegetables, corn, soybean, alfalfa, and iris among others. Description of Damage (larvae and adults): Redlegged grasshoppers are leaf chewers primarily feeding on leaves, sometimes causing total defoliation of the host plant leaves by chewing most leaf tissue but leaving the tougher veins. -
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NUTRIENT RESOURCES AND STOICHIOMETRY AFFECT THE ECOLOGY OF ABOVE- AND BELOWGROUND INVERTEBRATE CONSUMERS by JAYNE LOUISE JONAS B.S., Wayne State College, 1998 M.S., Kansas State University, 2000 AN ABSTRACT OF A DISSERTATION submitted in partial fulfillment of the requirements for the degree DOCTOR OF PHILOSOPHY Division of Biology College of Arts and Sciences KANSAS STATE UNIVERSITY Manhattan, Kansas 2007 Abstract Aboveground and belowground food webs are linked by plants, but their reciprocal influences are seldom studied. Because phosphorus (P) is the primary nutrient associated with arbuscular mycorrhizal (AM) symbiosis, and evidence suggests it may be more limiting than nitrogen (N) for some insect herbivores, assessing carbon (C):N:P stoichiometry will enhance my ability to discern trophic interactions. The objective of this research was to investigate functional linkages between aboveground and belowground invertebrate populations and communities and to identify potential mechanisms regulating these interactions using a C:N:P stoichiometric framework. Specifically, I examine (1) long-term grasshopper community responses to three large-scale drivers of grassland ecosystem dynamics, (2) food selection by the mixed-feeding grasshopper Melanoplus bivittatus, (3) the mechanisms for nutrient regulation by M. bivittatus, (4) food selection by fungivorous Collembola, and (5) the effects of C:N:P on invertebrate community composition and aboveground-belowground food web linkages. In my analysis of grasshopper community responses to fire, bison grazing, and weather over 25 years, I found that all three drivers affected grasshopper community dynamics, most likely acting indirectly through effects on plant community structure, composition and nutritional quality. In a field study, the diet of M. -
The Feasibility of Use of Caecal and Diverticular Coloration in Field Determination of Grasshopper Diet
The Great Lakes Entomologist Volume 4 Number 1 -- Spring 1971 Number 1 -- Spring Article 4 1971 July 2017 The Feasibility of Use of Caecal and Diverticular Coloration in Field Determination of Grasshopper Diet Michael Tyrkus Wayne State University Follow this and additional works at: https://scholar.valpo.edu/tgle Part of the Entomology Commons Recommended Citation Tyrkus, Michael 2017. "The Feasibility of Use of Caecal and Diverticular Coloration in Field Determination of Grasshopper Diet," The Great Lakes Entomologist, vol 4 (1) Available at: https://scholar.valpo.edu/tgle/vol4/iss1/4 This Peer-Review Article is brought to you for free and open access by the Department of Biology at ValpoScholar. It has been accepted for inclusion in The Great Lakes Entomologist by an authorized administrator of ValpoScholar. For more information, please contact a ValpoScholar staff member at [email protected]. Tyrkus: The Feasibility of Use of Caecal and Diverticular Coloration in F THE MICHIGAN ENTOMOLOGIST Vol. 4, No. 1 THE FEASIBILITY OF USE OF CAECAL AND DIVERTICULAR COLORATION IN FIELD DETERMINATION OF GRASSHOPPER DIET',' Michael Tyrkus Department of Biology, Wayne State University, Detroit, Michigan 48202 INTRODUCTION Many studies have been undertaken in the past on the food selection, food preferences, and economic damage of various grasshoppers and their allies. Among the more salient of these researches are those of Anderson (1961, 1964); Ball (1 936); Bindra (1958); Boldyrev (1928); Blackith and Blackith (1966); Brues (1946); Chapman (1957); Dibble (1940); Gangwere (1959, 1960, 1961, 1965, 1965a, 1966, 1966a, 1967);Husain etal. (1946); Isely (1938, 1946); Isely and Alexander (1949); Joyce (1952); Mulkern and Anderson (1959); Mulkern, Anderson, and Brusven (1962); Mulkern et al. -
Forms of Melanoplus Bowditchi (Orthoptera: Acrididae) Collected from Different Host Plants Are Indistinguishable Genetically and in Aedeagal Morphology
Forms of Melanoplus bowditchi (Orthoptera: Acrididae) collected from diVerent host plants are indistinguishable genetically and in aedeagal morphology Muhammad Irfan Ullah1,4 , Fatima Mustafa1,5 , Kate M. Kneeland1, Mathew L. Brust2, W. Wyatt Hoback3,6 , Shripat T. Kamble1 and John E. Foster1 1 Department of Entomology, University of Nebraska, Lincoln, NE, USA 2 Department of Biology, Chadron State College, Chadron, NE, USA 3 Department of Biology, University of Nebraska, Kearney, NE, USA 4 Current aYliation: Department of Entomology, University of Sargodha, Pakistan 5 Current aYliation: Department of Entomology, University of Agriculture Faisalabad, Pakistan 6 Current aYliation: Entomology and Plant Pathology Department, Oklahoma State University, Stillwater, OK, USA ABSTRACT The sagebrush grasshopper, Melanoplus bowditchi Scudder (Orthoptera: Acrididae), is a phytophilous species that is widely distributed in the western United States on sagebrush species. The geographical distribution of M. bowditchi is very similar to the range of its host plants and its feeding association varies in relation to sagebrush dis- tribution. Melanoplus bowditchi bowditchi Scudder and M. bowditchi canus Hebard were described based on their feeding association with diVerent sagebrush species, sand sagebrush and silver sagebrush, respectively. Recently, M. bowditchi have been observed feeding on other plant species in western Nebraska. We collected adult M. bowditchi feeding on four plant species, sand sagebrush, Artemisia filifolia, big sagebrush, A. tridentata, fringed sagebrush, A. frigidus, and winterfat, Kraschenin- Submitted 10 January 2014 nikovia lanata. We compared the specimens collected from the four plant species for Accepted 17 May 2014 Published 10 June 2014 their morphological and genetic diVerences. We observed no consistent diVerences among the aedeagal parameres or basal rings among the grasshoppers collected Corresponding author W. -
SYNAPOMORPHIES ORTHOPTERA, Sensu Stricto Grasshoppers
The Orthopteridan Orders Orthoptera Phasmatodea Plecoptera PLECOPTERIDA Embioptera Zoraptera Dermaptera POLYORTHOPTERA Grylloblattodea Mantophasmatodea Phasmatodea ORTHOPTERIDA Orthoptera Blattodea Perhaps similar Isoptera development of the gonoplac over 2nd DICTYOPTERA valvulae Mantodea Plecoptera PLECOPTERIDA Embioptera Zoraptera Dermaptera Grylloblattodea Mantophasmatodea Phasmatodea ORTHOPTERIDA Orthoptera • Second valvula reduced, with developmentBlattodea of gonoplac as functional ovipositor • Enlarged precostal field in forewingIsoptera DICTYOPTERA Mantodea ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas What is a “Weta”? A giant cricket! New Zealand Maori name of wetapunga that was given to the giant weta. Wetapunga translates roughly to "God of ugly things.” Wetas and king crickets occur principally in New Zealand and Australia. Can reach 90 mm (3.5 in) and 70 grams (2.5 oz). Orthoptera Ensifera Stenopelmatoidea Anostostomatidae ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas SYNAPOMORPHIES • Lateral flange of pronotum largely covering pleuron, which • Hind leg modified for jumping correspondingly becomes by straightening of femoral/tibial desclerotized joint (cryptopleuron) • Femur enlarged to • Hind tibia with 2 dorsal accommodate large tibia rows of teeth extensor muscle ORTHOPTERA, sensu stricto Grasshoppers, Locusts, Katydids, Crickets, Wetas SYNAPOMORPHIES • First thoracic spiracle horizontally divided • Wings inclined over abdomen at rest • Wing pads of late nymphal