Orthoptera: Acrididae) from Turkey with Description of a New Species
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ARTHROPOD COMMUNITIES and PASSERINE DIET: EFFECTS of SHRUB EXPANSION in WESTERN ALASKA by Molly Tankersley Mcdermott, B.A./B.S
Arthropod communities and passerine diet: effects of shrub expansion in Western Alaska Item Type Thesis Authors McDermott, Molly Tankersley Download date 26/09/2021 06:13:39 Link to Item http://hdl.handle.net/11122/7893 ARTHROPOD COMMUNITIES AND PASSERINE DIET: EFFECTS OF SHRUB EXPANSION IN WESTERN ALASKA By Molly Tankersley McDermott, B.A./B.S. A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biological Sciences University of Alaska Fairbanks August 2017 APPROVED: Pat Doak, Committee Chair Greg Breed, Committee Member Colleen Handel, Committee Member Christa Mulder, Committee Member Kris Hundertmark, Chair Department o f Biology and Wildlife Paul Layer, Dean College o f Natural Science and Mathematics Michael Castellini, Dean of the Graduate School ABSTRACT Across the Arctic, taller woody shrubs, particularly willow (Salix spp.), birch (Betula spp.), and alder (Alnus spp.), have been expanding rapidly onto tundra. Changes in vegetation structure can alter the physical habitat structure, thermal environment, and food available to arthropods, which play an important role in the structure and functioning of Arctic ecosystems. Not only do they provide key ecosystem services such as pollination and nutrient cycling, they are an essential food source for migratory birds. In this study I examined the relationships between the abundance, diversity, and community composition of arthropods and the height and cover of several shrub species across a tundra-shrub gradient in northwestern Alaska. To characterize nestling diet of common passerines that occupy this gradient, I used next-generation sequencing of fecal matter. Willow cover was strongly and consistently associated with abundance and biomass of arthropods and significant shifts in arthropod community composition and diversity. -
Catalogue of the Type Specimens Deposited in the Department of Entomology, National Museum, Prague, Czech Republic*
ACTA ENTOMOLOGICA MUSEI NATIONALIS PRAGAE Published 30.iv.2014 Volume 54(1), pp. 399–450 ISSN 0374-1036 http://zoobank.org/urn:lsid:zoobank.org:pub:7479D174-4F1D-4465-9EEA-2BBB5E1FC2A2 Catalogue of the type specimens deposited in the Department of Entomology, National Museum, Prague, Czech Republic* Polyneoptera Lenka MACHÁýKOVÁ & Martin FIKÁýEK Department of Entomology, National Museum in Prague, Kunratice 1, CZ-148 00 Praha 4-Kunratice, Czech Republic & Department of Zoology, Faculty of Sciences, Charles University in Prague, Viniþná 7, CZ-128 43, Praha 2, Czech Republic; e-mails: [email protected]; m¿ [email protected] Abstract. Type specimens from the collection of the polyneopteran insect orders (Dermaptera, Blattodea, Orthoptera, Phasmatodea) deposited in the Department of Entomology, National Museum, Prague are catalogued. We provide precise infor- mation about types of 100 taxa (5 species of Dermaptera, 3 species of Blattodea, 4 species of Phasmatodea, 55 species of Caelifera, and 33 species of Ensifera), including holotypes of 38 taxa. The year of publication of Calliptamus tenuicer- cis anatolicus MaĜan, 1952 and Calliptamus tenuicercis iracus MaĜan, 1952 are corrected. The authorship of the names traditionally ascribed to J. Obenberger is discussed in detail. Only the name Podisma alpinum carinthiacum Obenberger, 1926 is available since the publication by OBENBERGER (1926a). ‘Stenobothrus (Stauroderus) biguttulus ssp. bicolor Charp. 1825’ and ‘Stenobothrus (Stau- roderus) ssp. collinus Karny’ sensu OBENBERGER (1926a,b) refer to Gryllus bicolor Charpentier, 1825 and Stauroderus biguttulus var. collina Karny, 1907, respectively, which both have to be considered available already since their original descriptions by CHARPENTIER (1825) and KARNY (1907). Key words. -
Clubhorned Grasshopper Aeropedellus Clavatus (Thomas)
Wyoming_________________________________________________________________________________________ Agricultural Experiment Station Bulletin 912 • Species Fact Sheet September 1994 Clubhorned Grasshopper Aeropedellus clavatus (Thomas) Distribution and Habitat and North Dakota it is frequently abundant in The clubhorned grasshopper, Aeropedellus clavatus grasshopper assemblages infesting rangeland. (Thomas), inhabits grasslands of western Canada and the northern United States and extends its range into Food Habits mountainous areas as far south as Arizona and New The clubhorned grasshopper feeds on grasses and Mexico. In Colorado, one resident population survives sedges. Examinations of crop contents show that in above timberline at 13,600 feet in a rocky, grass-sedge mixedgrass prairie this grasshopper feeds on western habitat. In the prairie provinces of Canada it is the most wheatgrass, prairie junegrass, Sandberg bluegrass, widely distributed and abundant of the grassland species, needleandthread, threadleaf sedge, and needleleaf sedge. occurring on all dry and somewhat sandy areas south of the In mountain meadows and parks different groups of boreal forest. In four of ten years it was the dominant grasses and sedges are used for food. Wherever species of a grasshopper assemblage inhabiting the sand Kentucky bluegrass has invaded an area, it is a preferred prairie of southeastern North Dakota. host plant. When grass seeds and glumes become available in the habitat, they are fed upon heavily. The Economic Importance clubhorned grasshopper is known to feed upon 28 The clubhorned grasshopper is primarily a pest of species of grasses and six species of sedges. Small grasses and sedges in the mixedgrass and bunchgrass amounts of forbs, fungi, pollen, and arthropod parts prairies and in mountain meadows and parks. -
The Transcriptomic and Genomic Architecture of Acrididae Grasshoppers
The Transcriptomic and Genomic Architecture of Acrididae Grasshoppers Dissertation To Fulfil the Requirements for the Degree of “Doctor of Philosophy” (PhD) Submitted to the Council of the Faculty of Biological Sciences of the Friedrich Schiller University Jena by Bachelor of Science, Master of Science, Abhijeet Shah born on 7th November 1984, Hyderabad, India 1 Academic reviewers: 1. Prof. Holger Schielzeth, Friedrich Schiller University Jena 2. Prof. Manja Marz, Friedrich Schiller University Jena 3. Prof. Rolf Beutel, Friedrich Schiller University Jena 4. Prof. Frieder Mayer, Museum für Naturkunde Leibniz-Institut für Evolutions- und Biodiversitätsforschung, Berlin 5. Prof. Steve Hoffmann, Leibniz Institute on Aging – Fritz Lipmann Institute, Jena 6. Prof. Aletta Bonn, Friedrich Schiller University Jena Date of oral defense: 24.02.2020 2 Table of Contents Abstract ........................................................................................................................... 5 Zusammenfassung............................................................................................................ 7 Introduction ..................................................................................................................... 9 Genetic polymorphism ............................................................................................................. 9 Lewontin’s paradox ....................................................................................................................................... 9 The evolution -
Comparison of Gene Expression in the Red Imported Fire Ant, Solenopsis Invicta, in Different Temperature Conditions
Comparison of Gene Expression in the Red Imported Fire Ant, Solenopsis Invicta, in Different Temperature Conditions Youngjin Park ( [email protected] ) Animal and Plant Quarantine Agency Mohammad Vatanparast Animal and Plant Quarantine Agency Robert Puckett Texas A&M University Deuk-Soo Choi Animal and Plant Quarantine Agency Research Article Keywords: Solenopsis invicta, RIFA, transcriptome, RNA-seq, KEGG pathway, differentially expressed gene Posted Date: March 1st, 2021 DOI: https://doi.org/10.21203/rs.3.rs-255031/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Version of Record: A version of this preprint was published at Scientic Reports on August 13th, 2021. See the published version at https://doi.org/10.1038/s41598-021-95779-w. Page 1/21 Abstract The red imported re ant (RIFA), Solenopsis invicta Buren is native to South America and is known as a global problematic invasive species. This study focused on the molecular response of RIFA by comparing gene expression proles after exposing ants to low (10℃) and high (40℃) temperature stress and comparing to untreated controls (30℃). A total of 99,085 unigenes were obtained, of which 19,154 were annotated with gene descriptions, gene ontology terms, and metabolic pathways. 86 gene ontology (GO) functional sub-groups and 23 EggNOG terms resulted. Differentially expressed genes (DEGs) with log2FC ≥ 10 were screened and were compared at different temperatures. We found 203, 48, and 66 specic DEGs co-regulated at 10, 20, and 40℃. Comparing transcriptome proles for differential gene expression resulted in various DE proteins and genes, including cytochrome P450, NADH dehydrogenase subunit 1, cuticle protein and heat shock protein (HSP) which have previously been reported to be involved in cold and high temperature resistance. -
The Taxonomy of Utah Orthoptera
Great Basin Naturalist Volume 14 Number 3 – Number 4 Article 1 12-30-1954 The taxonomy of Utah Orthoptera Andrew H. Barnum Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Barnum, Andrew H. (1954) "The taxonomy of Utah Orthoptera," Great Basin Naturalist: Vol. 14 : No. 3 , Article 1. Available at: https://scholarsarchive.byu.edu/gbn/vol14/iss3/1 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. IMUS.COMP.ZSOL iU6 1 195^ The Great Basin Naturalist harvard Published by the HWIilIijM i Department of Zoology and Entomology Brigham Young University, Provo, Utah Volum e XIV DECEMBER 30, 1954 Nos. 3 & 4 THE TAXONOMY OF UTAH ORTHOPTERA^ ANDREW H. BARNUM- Grand Junction, Colorado INTRODUCTION During the years of 1950 to 1952 a study of the taxonomy and distribution of the Utah Orthoptera was made at the Brigham Young University by the author under the direction of Dr. Vasco M. Tan- ner. This resulted in a listing of the species found in the State. Taxonomic keys were made and compiled covering these species. Distributional notes where available were made with the brief des- criptions of the species. The work was based on the material in the entomological col- lection of the Brigham Young University, with additional records obtained from the collection of the Utah State Agricultural College. -
President's Message
ISSN 2372-2517 (Online), ISSN 2372-2479 (Print) METALEPTEAMETALEPTEA THE NEWSLETTER OF THE ORTHOPTERISTS’ SOCIETY TABLE OF CONTENTS President’s Message (Clicking on an article’s title will take you By DAVID HUNTER to the desired page) President [email protected] [1] PRESIDENT’S MESSAGE [2] SOCIETY NEWS ear Fellow Orthopterists! [2] Call for the 2020 Theodore J. Cohn Research Fund by M. LECOQ [2] Grants supporting the Orthoptera Species As I am writing this File by M.M. CIGLIANO from Canberra, the sky is [3] A call for manuscripts Special Issue “Locusts and Grasshoppers: Biology, Ecology and Man- filled with dense smoke agement” by A.V. LATCHININSKY D from the catastrophic [3] A call for DNA-grade specimens to recon- D sruct a comprehensive phylogeny of Ensifera fires we have had in Australia this by H. SONG fire season. Continuing drought and [4] Updates from the GLI by R. OVERSON [5] Reminder: Seeking Speakers for the 2020 weeks of unusually high temperatures ICE Symposium: “Polyneoptera for our Planet” have led to widespread fires covering by D.A. WOLLER ET AL. [5] REGIONAL REPORTS millions of hectares: as of the first [5] East Europe - North and Central Asia by week in January, 6.3 million ha have M.G. SERGEEV [6] Central & Southern Africa burnt which is just under half the area by V. COULDRIDGE of England! A catastrophic situation [8] T.J. COHN GRANT REPORTS indeed! [8] On the study of gregarine parasites in Orthoptera by J.H. MEDINA DURÁN Our society continues our support [10] Genetic diversity in populations of for research through OSF grants and Anonconotus italoaustriacus Nadig, 1987 (Insecta, Orthoptera) in North-East Italy by F. -
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. -
Field Guide to Some of the Common Grasshoppers of the Front Range of Colorado
Field guide to some of the common grasshoppers of the Front Range of Colorado Instructions: The following guide presents the grasshopper species most commonly found along an elevational gradient from the plains of Boulder, Colorado, to the subalpine that lies to the west. Use this guide to identify the species that are found during each weekly sample at your designated site. This will help you determine whether climate change is impacting the timing to adulthood of each community. Grasshoppers of the Front Range There are 548 species of North American grasshoppers and 133 of these occur in Colorado. Only about a dozen of these species are considered important pests on rangelands, with five of these causing most problems on crops. Within the Front Range of Colorado, 72 species can be found, although most are relatively uncommon. The most commonly encountered species along our lower foothills (1752m) to subalpine (3000 m) transect can be placed into 3 groups (subfamilies); Gomphocerinae, Melanoplinae and Oedipodinae. The Gomphocerinae (slant-faced grasshoppers) are grass specialists that tend to be small and are the grasshoppers commonly heard in meadows chorusing during the day. The Melanoplinae (spur-throated grasshoppers) are the most commonly encountered grasshoppers and are primarily forb feeders. Melanoplinae are small (but some can be large) and several of these species tend to be short winged and cannot actively fly, They do not chorus. Most of the Oedipodinae (banded-winged grasshoppers) tend to be grass feeders or herbivorous (both grass and forb feeding) and are rarely solely forb feeders. These grasshoppers are commonly found in open areas where they bask and display, they vary considerably in size, and are all active fliers that often use their wings to make loud clicking sounds. -
Evolution, Discovery, and Interpretations of Arthropod Mushroom Bodies Nicholas J
Downloaded from learnmem.cshlp.org on September 28, 2021 - Published by Cold Spring Harbor Laboratory Press Evolution, Discovery, and Interpretations of Arthropod Mushroom Bodies Nicholas J. Strausfeld,1,2,5 Lars Hansen,1 Yongsheng Li,1 Robert S. Gomez,1 and Kei Ito3,4 1Arizona Research Laboratories Division of Neurobiology University of Arizona Tucson, Arizona 85721 USA 2Department of Ecology and Evolutionary Biology University of Arizona Tucson, Arizona 85721 USA 3Yamamoto Behavior Genes Project ERATO (Exploratory Research for Advanced Technology) Japan Science and Technology Corporation (JST) at Mitsubishi Kasei Institute of Life Sciences 194 Machida-shi, Tokyo, Japan Abstract insect orders is an acquired character. An overview of the history of research on the Mushroom bodies are prominent mushroom bodies, as well as comparative neuropils found in annelids and in all and evolutionary considerations, provides a arthropod groups except crustaceans. First conceptual framework for discussing the explicitly identified in 1850, the mushroom roles of these neuropils. bodies differ in size and complexity between taxa, as well as between different castes of a Introduction single species of social insect. These Mushroom bodies are lobed neuropils that differences led some early biologists to comprise long and approximately parallel axons suggest that the mushroom bodies endow an originating from clusters of minute basophilic cells arthropod with intelligence or the ability to located dorsally in the most anterior neuromere of execute voluntary actions, as opposed to the central nervous system. Structures with these innate behaviors. Recent physiological morphological properties are found in many ma- studies and mutant analyses have led to rine annelids (e.g., scale worms, sabellid worms, divergent interpretations. -
Orthoptera: Acrididae)
bioRxiv preprint doi: https://doi.org/10.1101/119560; this version posted March 22, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 2 Ecological drivers of body size evolution and sexual size dimorphism 3 in short-horned grasshoppers (Orthoptera: Acrididae) 4 5 Vicente García-Navas1*, Víctor Noguerales2, Pedro J. Cordero2 and Joaquín Ortego1 6 7 8 *Corresponding author: [email protected]; [email protected] 9 Department of Integrative Ecology, Estación Biológica de Doñana (EBD-CSIC), Avda. Américo 10 Vespucio s/n, Seville E-41092, Spain 11 12 13 Running head: SSD and body size evolution in Orthopera 14 1 bioRxiv preprint doi: https://doi.org/10.1101/119560; this version posted March 22, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 15 Sexual size dimorphism (SSD) is widespread and variable in nature. Although female-biased 16 SSD predominates among insects, the proximate ecological and evolutionary factors promoting 17 this phenomenon remain largely unstudied. Here, we employ modern phylogenetic comparative 18 methods on 8 subfamilies of Iberian grasshoppers (85 species) to examine the validity of 19 different models of evolution of body size and SSD and explore how they are shaped by a suite 20 of ecological variables (habitat specialization, substrate use, altitude) and/or constrained by 21 different evolutionary pressures (female fecundity, strength of sexual selection, length of the 22 breeding season). -
B Chromosomes in Grasshoppers: Different Origins and Pathways to the Modern Bs
G C A T T A C G G C A T genes Article B Chromosomes in Grasshoppers: Different Origins and Pathways to the Modern Bs Ilyas Yerkinovich Jetybayev 1,2,* , Alexander Gennadievich Bugrov 2,3, Victoria Vladimirovna Dzyubenko 3 and Nikolay Borisovich Rubtsov 1,3 1 The Federal Research Center Institute of Cytology and Genetics, Russian Academy of Sciences, Siberian Branch, Lavrentjev Ave., 10, 630090 Novosibirsk, Russia; [email protected] 2 Institute of Systematics and Ecology of Animals, Russian Academy of Sciences, Siberian Branch, Frunze str. 11, 630091 Novosibirsk, Russia; [email protected] 3 Novosibirsk State University, Pirogov str., 2, 630090 Novosibirsk, Russia; [email protected] * Correspondence: [email protected]; Tel.: +7-383-363-49-63 (ext. 1027) Received: 28 August 2018; Accepted: 11 October 2018; Published: 18 October 2018 Abstract: B chromosomes (Bs) were described in most taxa of eukaryotes and in around 11.9% of studied Orthopteran species. In some grasshopper species, their evolution has led to many B chromosome morphotypes. We studied the Bs in nine species (Nocaracris tardus, Nocaracris cyanipes, Aeropus sibiricus, Chorthippus jacobsoni, Chorthippus apricarius, Bryodema gebleri, Asiotmethis heptapotamicus songoricus, Podisma sapporensis, and Eyprepocnemis plorans), analyzing their possible origin and further development. The studied Bs consisted of C-positive or C-positive and C-negative regions. Analyzing new data and considering current hypotheses, we suggest that Bs in grasshoppers could arise through different mechanisms and from different chromosomes of the main set. We gave our special attention to the Bs with C-negative regions and suggest a new hypothesis of B chromosome formation from large or medium autosomes.